Table 2 QTLs surpassing the significance threshold (P < 5 × 10−7) for evidence of an association with the multifocal lesions.
BTA1 | QTL start (bp) | QTL end (bp) | P value most significant SNP | SNP position2 | Annotation | Genes in QTL3 | No of significant SNPs in QTL |
---|---|---|---|---|---|---|---|
3 | 24233907 | 25325344 | 1.50E−07 | 24825344 | Intergenic | TBX15, U6, SPAG17, GDAP2, WDR3, ENSBTAG00000048491, ENSBTAG00000051931 | 12 |
5 | 24941743 | 26254968 | 1.39E−08 | 25667192 | Intron | VEZT, METAP2, USP44, MUCL1, GLYCAM1, PPP1R1A, PDE1B, NCKAP1L, ZNF385A, GTSF1, GPR84, ITGA5, COPZ1, NFE2, HNRNPA1, CBX5, SMUG1, HOXC5, HOXC4, HOXC6, HOXC13, HOXC8, HOXC9, HOXC10, HOXC11, HOXC12, U6, ENSBTAG00000052805, ENSBTAG00000053941, ENSBTAG00000029988, ENSBTAG00000049200, ENSBTAG00000023670 ,ENSBTAG00000049405, ENSBTAG00000010711, ENSBTAG00000053336, ENSBTAG00000049915, ENSBTAG00000049837, ENSBTAG00000048717, ENSBTAG00000052958, ENSBTAG00000055223, ENSBTAG0000005385, ENSBTAG00000036381, ENSBTAG00000053232, ENSBTAG00000029788, ENSBTAG00000053186, ENSBTAG00000052715, ENSBTAG00000052501, ENSBTAG00000051607, ENSBTAG00000051555 | 24 |
5 | 38788039 | 39790008 | 2.04E−07 | 39288039 | Intron | PDZRN4, CNTN1, ENSBTAG00000001079 | 2 |
5 | 23274617 | 24292059 | 4.92E−07 | 23774617 | Intergenic | UBE2N, MRPL42, SOCS2, CRADD, PLXNC1, CEP83, TMCC3, ENSBTAG00000033531, ENSBTAG00000049886, ENSBTAG00000053589, ENSBTAG00000050045, ENSBTAG00000052916 | 5 |
5 | 27260957 | 28354826 | 1.69E−08 | 27777338 | Intergenic | KRT77, KRT1, KRT2, KRT73, KRT72, KRT74, KRT5, KRT6A, KRT6B, KRT75, KRT82, KRT84, KRT85, KRT89, KRT83, KRT81, KRT7, KRT80, SMIM41, ATG101, NR4A1, TAMALIN, ACVR1B, ACVRL1, ANKRD33, FIGNL2, SCN8A, U6, SLC4A8, ENSBTAG00000054953, ENSBTAG00000040019, ENSBTAG00000052798, ENSBTAG00000054816, ENSBTAG00000054136, ENSBTAG00000016166, ENSBTAG00000049194, ENSBTAG00000023471 | 6 |
11 | 12914642 | 14422761 | 1.01E−07 | 13611793 | Intron | DYSF, ZNF638, PAIP2B, ATP6V1B1, FIGLA, NAGK, VAX2, CLEC4F, TEX261, CD207, ANKRD53, ADD2, TGFA, FAM136A, XDH, SRD5A2, ENSBTAG00000048791, ENSBTAG00000051968, ENSBTAG00000050557, ENSBTAG00000051045 | 4 |
11 | 5223771 | 6618872 | 1.66E−11 | 5755689 | Intergenic | AFF3, CHST10, NMS, PDCL3, NPAS2, TBC1D8, CNOT11, RFX8, RNF149, CREG2, MAP4K4, ENSBTAG00000050215, ENSBTAG00000043158, ENSBTAG00000054755 | 7 |
11 | 9416584 | 10698629 | 1.98E−07 | 9916584 | Intergenic | TACR1, POLE4, U6, HK2, SEMA4F, M1AP, RTKN, DOK1, MRPL53, LOXL3, WBP1, DCTN1, HTRA2, WDR54, AUP1, DOX1, C11H2orf81, MGC152281, TLX2, PCGF1, LBX2, CCDC142, MOGS, INO80B, SLC4A5, MOB1A, MTHFD2, BOLA3, TET3, DGUOK, ENSBTAG00000049427 , ENSBTAG00000050345, ENSBTAG00000010072, ENSBTAG00000050408, ENSBTAG00000049783 | 3 |
22 | 5865513 | 6865513 | 4.85E−07 | 6365513 | Intron | STT3B, OSBPL10, GPD1L, CMTM8, CMTM7, ENSBTAG00000050895 | 1 |
22 | 2638700 | 4937859 | 8.62E−10 | 3138700 | Intergenic | CMC1, AZI2, RBMS3, bta-mir-11990, U6, ENSBTAG00000022751, ENSBTAG00000050982, ENSBTAG00000048601, ENSBTAG00000052346 | 15 |
22 | 1280377 | 2574848 | 1.50E−10 | 2008232 | Intergenic | U1, SEC61G, NEK10, U6, SLC4A7, 5S_rRNA, EOMES | 18 |
23 | 17326599 | 18326599 | 4.92E−07 | 17826599 | Intergenic | VEGFA, U6, MYMX, SPATS1, TMEM63B, HSP90AB1, CDC5L, CAPN11, NFKBIE, SLC9A1, SLC35B2, TMEM151B, AARS2, SUPT3H, 5S-rRNA, ENSBTAG00000050989, ENSBTAG00000049965, ENSBTAG00000050049, ENSBTAG00000050249, ENSBTAG00000050117, ENSBTAG00000053551, ENSBTAG00000053897 | 1 |
24 | 37183179 | 38191028 | 2.33E−07 | 37683179 | Intron | EMILIN2, LPIN2, MYOM1, MYL12A, MYL12B, TGIF1, DLGAP1, SNORA70, ENSBTAG00000052283 | 31 |