| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12266842-12266993 | Rare:66 | ||||
| chr12:12267210-12267398 | Common:5; Rare:82 | ||||
| chr12:12350212-12350477 | Common:1; Rare:85 | ||||
| chr12:12356956-12357212 | Common:4; Rare:125 | ||||
| chr12:12611627-12612025 | Common:2; Rare:119 | ||||
| chr12:12684464-12684731 | Common:1; Rare:37 | ||||
| chr12:12696148-12696286 | Rare:38 | ||||
| chr12:12696634-12696768 | Rare:41 | ||||
| chr12:12717244-12717509 | Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725565-12726065 | Common:6; Rare:124 | ||||
| chr12:12891451-12891567 | Rare:29 | ||||
| chr12:13000207-13000491 | Common:2; Rare:91 | ||||
| chr12:13044290-13044403 | Rare:25 | ||||
| chr12:14365490-14365785 | Common:1; Rare:93 | ||||
| chr12:14384957-14385397 | Common:1; Rare:83 |