| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6493486-6493618 | Common:3; Rare:20 | ||||
| chr12:6493778-6494126 | Common:2; Rare:104 | ||||
| chr12:6534325-6534582 | Common:5; Rare:112 | ||||
| chr12:6568260-6568382 | Rare:46 | ||||
| chr12:6598010-6598360 | Common:1; Rare:88 | ||||
| chr12:6631594-6631736 | Common:1; Rare:32 | ||||
| chr12:6663071-6663380 | Common:1; Rare:90 | ||||
| chr12:6688879-6689195 | Rare:100 | ||||
| chr12:6689250-6689336 | Rare:25 | ||||
| chr12:6689343-6689760 | Common:3; Rare:111 | ||||
| chr12:6723828-6724295 | Common:1; Rare:103 | ||||
| chr12:6752932-6753189 | Common:6; Rare:78 | ||||
| chr12:6851255-6851492 | Rare:51 | ||||
| chr12:6851912-6852191 | Rare:72 | ||||
| chr12:6867355-6867680 | Common:2; Rare:152; Clinvar:2; Clinvar (benign):2 |