| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100573811-100574211 | Common:6; Rare:99 | ||||
| chr12:101279680-101280593 | Common:7; Rare:370 | ||||
| chr12:101406628-101407028 | Common:7; Rare:76 | ||||
| chr12:101407250-101407502 | Rare:69 | ||||
| chr12:101407487-101408324 | Common:20; Rare:818 | ||||
| chr12:101408287-101408687 | Common:2; Rare:64 | ||||
| chr12:101696773-101697330 | Common:7; Rare:146 | ||||
| chr12:101697340-101698030 | Common:27; Rare:1034 | ||||
| chr12:101698109-101698280 | Common:2; Rare:71 | ||||
| chr12:101830770-101831204 | Common:6; Rare:361; Clinvar (benign):6 | ||||
| chr12:101876693-101877400 | Common:33; Rare:356 | ||||
| chr12:101877320-101877780 | Common:15; Rare:467 | ||||
| chr12:102061590-102062337 | Common:7; Rare:437 | ||||
| chr12:102119131-102119859 | Common:6; Rare:153 | ||||
| chr12:102119960-102120738 | Common:13; Rare:821 |