| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115625972-115626247 | Rare:83 | ||||
| chr5:115841780-115842027 | Common:4; Rare:84 | ||||
| chr5:116084883-116085089 | Common:7; Rare:90 | ||||
| chr5:119070840-119071191 | Common:4; Rare:107 | ||||
| chr5:119268614-119268887 | Common:1; Rare:73 | ||||
| chr5:119355712-119356003 | Common:4; Rare:79 | ||||
| chr5:120465480-120465669 | Common:2; Rare:54 | ||||
| chr5:121961700-121962053 | Common:15; Rare:130 | ||||
| chr5:122076897-122077257 | Common:1; Rare:81 | ||||
| chr5:122077318-122077708 | Common:1; Rare:143; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:122077775-122078445 | Common:1; Rare:191; Clinvar:1 | ||||
| chr5:122078470-122078715 | Rare:50 | ||||
| chr5:122775156-122775208 | Rare:17 | ||||
| chr5:122845516-122845684 | Common:3; Rare:66 | ||||
| chr5:123036447-123036536 | Rare:39 |