| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:81761520-81761567 | Not yet | Common:4; Rare:8; Clinvar (benign):1 | 36 | ||
| chr3:101676275-101676490 | Not yet | Common:1; Rare:71 | 133 | ||
| chr3:107240630-107240761 | Not yet | Rare:53 | 91 | ||
| chr3:119517128-119517229 | Not yet | Common:2; Rare:29 | 117 | ||
| chr3:130111485-130111776 | Not yet | Common:3; Rare:68 | 147 | ||
| chr3:131361648-131361904 | Not yet | Common:3; Rare:77 | 162 | ||
| chr3:141660275-141660365 | Not yet | Rare:28 | 80 | ||
| chr3:150408860-150409008 | Not yet | Rare:44 | 91 | ||
| chr3:151460702-151460837 | Not yet | Rare:40 | 139 | ||
| chr3:151770111-151770427 | Not yet | Common:4; Rare:50 | 222 | ||
| chr3:169659509-169659816 | Not yet | Common:1; Rare:56 | 172 | ||
| chr3:169765053-169765222 | Not yet | Rare:71; Clinvar (pathogenic):2 | 152 | ||
| chr3:194583866-194584020 | Not yet | Common:10; Rare:56 | 141 | ||
| chr3:195657868-195658110 | Not yet | Common:12; Rare:38 | 120 | ||
| chr3:195990260-195990419 | Not yet | Rare:21 | 110 |