| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50763720-50764720 | Common:34; Rare:1206 | ||||
| chr12:50764746-50765171 | Common:3; Rare:174 | ||||
| chr12:50923784-50924184 | Common:2; Rare:74 | ||||
| chr12:50924248-50924418 | Common:1; Rare:22 | ||||
| chr12:50924380-50924780 | Common:15; Rare:437 | ||||
| chr12:50924800-50925140 | Common:4; Rare:161 | ||||
| chr12:50925103-50925545 | Common:2; Rare:294 | ||||
| chr12:51024720-51025926 | Common:13; Rare:677 | ||||
| chr12:51025831-51026840 | Common:35; Rare:1002; Clinvar:18; Clinvar (benign):14 | ||||
| chr12:51047580-51048119 | Common:13; Rare:251 | ||||
| chr12:51048020-51048439 | Common:9; Rare:539 | ||||
| chr12:51048491-51049116 | Common:7; Rare:222 | ||||
| chr12:51082488-51083286 | Common:2; Rare:224 | ||||
| chr12:51083480-51083880 | Common:3; Rare:493 | ||||
| chr12:51172547-51173363 | Common:16; Rare:649 |