| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6493793-6494126 | Common:2; Rare:100 | ||||
| chr12:6568260-6568382 | Rare:46 | ||||
| chr12:6723970-6724158 | Rare:45 | ||||
| chr12:6752955-6753189 | Common:6; Rare:73 | ||||
| chr12:6851245-6851489 | Rare:57 | ||||
| chr12:6851893-6852180 | Rare:75 | ||||
| chr12:6867355-6867559 | Common:2; Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873334-6873534 | Common:1; Rare:54 | ||||
| chr12:6904644-6904839 | Common:1; Rare:43 | ||||
| chr12:6951266-6951379 | Rare:28 | ||||
| chr12:6970640-6970963 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr12:7109236-7109534 | Common:1; Rare:65 | ||||
| chr12:7130322-7130411 | Rare:16 | ||||
| chr12:7189563-7189735 | Rare:64; Clinvar:4 | ||||
| chr12:8032512-8032785 | Common:5; Rare:89 |