| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120194683-120194760 | Rare:29 | ||||
| chr12:120201081-120201354 | Common:2; Rare:88 | ||||
| chr12:120437877-120438139 | Common:2; Rare:86; Clinvar (benign):1 | ||||
| chr12:120446344-120446478 | Common:1; Rare:60 | ||||
| chr12:120469568-120469873 | Common:2; Rare:109 | ||||
| chr12:120495860-120496216 | Common:7; Rare:123 | ||||
| chr12:121399885-121400144 | Common:5; Rare:93 | ||||
| chr12:121802940-121803091 | Rare:35 | ||||
| chr12:121888632-121888868 | Common:2; Rare:76 | ||||
| chr12:122526911-122527329 | Common:3; Rare:141 | ||||
| chr12:122980571-122980916 | Common:2; Rare:101 | ||||
| chr12:123233093-123233490 | Common:2; Rare:132; Clinvar:1 | ||||
| chr12:123364825-123364983 | Common:3; Rare:58 | ||||
| chr12:123584317-123584609 | Common:6; Rare:97 | ||||
| chr12:123602039-123602144 | Common:3; Rare:35 |