| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:126988380-126988850 | Common:4; Rare:131 | ||||
| chr3:127590628-127591300 | Common:21; Rare:531 | ||||
| chr3:127597344-127597751 | Rare:141 | ||||
| chr3:127598087-127598489 | Common:18; Rare:575 | ||||
| chr3:127604690-127605090 | Common:2; Rare:150; Clinvar (benign):3 | ||||
| chr3:127628869-127629269 | Common:5; Rare:480 | ||||
| chr3:127672041-127672495 | Common:6; Rare:213 | ||||
| chr3:127672680-127673080 | Common:13; Rare:549 | ||||
| chr3:127673160-127673566 | Common:6; Rare:204 | ||||
| chr3:128051373-128051970 | Common:3; Rare:208 | ||||
| chr3:128052097-128052525 | Common:24; Rare:856 | ||||
| chr3:128123070-128123470 | Common:2; Rare:77 | ||||
| chr3:128123700-128124168 | Rare:600 | ||||
| chr3:128153217-128153623 | Common:6; Rare:412 | ||||
| chr3:128153633-128154033 | Common:7; Rare:213 |