Table 1 Genomic annotation of variants.

From: The role of neurotrophin genes involved in the vulnerability to gambling disorder

SNP

Gene

Genomic region

ENCODE Cis regulatory elements (CREs)

TF binding sites (JASPAR)

rs6332

NTF3

Synonymous variant

rs6489630

NTF3

Downstream gene variant

pELS (EH38E1589222)

rs7956189

NTF3

Downstream gene variant

WT1

rs12273363

BDNF

Upstream gene variant

pELS (EH38E1528854)

YY1

rs908867

BDNF

Upstream gene variant

rs1491850

BDNF

Intron variant

rs2274592

CNTFR

Intron variant

ZNF740, WT1, CTCF, Znf281

rs4363285

CNTFR

Intron variant

ELF3, SPIB, ELF1, EHF, CTCF

rs10814123

CNTFR

Intron variant

HFN1A, BARX2

rs3763614

CNTFR

Intron variant

Nr5a2

rs657770

NGFR

Intron variant

rs534561

NGFR (P75)

Intron variant

MZF1(var.2)

rs741073

NGFR (P75)

3 prime UTR variant

adjacent to a dELS (EH38E1868997)

KLF9, MSANTD3

rs11140783

NTRK2

Intron variant

Adjacent to a dELS (EH38E2702614)

IRF8, IRF4

rs1545285

NTRK2

Intron variant

Dmbx1, OTX2

rs4412435

NTRK2

Intron variant

dELS (EH38E2702692)

BACH2, NFE2L1, MAFK, JUN (var.2), MAF::NFE2, Smad2::Smad3

rs10868241

NTRK2

Intron variant

Prmd15

rs4361832

NTRK2

Intron variant

NFIA, MSGN1

rs12000011

NTRK2

Intron variant

WTF1, Gfi1b

rs1948308

NTRK2

Intron variant

HIC2, Nkx3-1

rs3739570

NTRK2

3 prime UTR variant

rs10780695

NTRK2

Downstream gene variant

Stat2, HOXC13

rs2117655

NTRK3

Intron variant

SOX15, SOX8

rs11638486

NTRK3

Intron variant

rs1435403

NTRK3

Intron variant

Arid5a

rs922232

NTRK3

Intron variant

HOXC13

rs2009853

NTRK3

Intron variant

-

rs1461210

NTRK3

Intron variant

rs1346164

NTRK3

Intron variant

GFI1, Gfi1b

rs744993

NTRK3-AS1

Upstream gene variant

ZFP42

rs6328

NFG-AS1

Intron variant

INSM1

rs6537860

NFG-AS1

Intron variant

ZKSCAN5

rs1800601

NTRK1

5 prime UTR variant

Prom (EH38E1388452)

rs1998977

NTRK1

Intron variant

DMRTC2

rs10908521

NTRK1

Intron variant

rs1800879

NTRK1

Intron variant

RELB