| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121712646-121712885 | Common:3; Rare:88 | ||||
| chr12:121802939-121803120 | Common:1; Rare:43 | ||||
| chr12:121803141-121803311 | Rare:49 | ||||
| chr12:121888634-121888863 | Common:2; Rare:75 | ||||
| chr12:122422547-122422807 | Common:4; Rare:86 | ||||
| chr12:122526868-122527301 | Common:4; Rare:152 | ||||
| chr12:122896066-122896221 | Rare:82 | ||||
| chr12:122980568-122980915 | Common:2; Rare:103 | ||||
| chr12:123233090-123233490 | Common:2; Rare:132; Clinvar:1 | ||||
| chr12:123268175-123268349 | Rare:34 | ||||
| chr12:123364821-123364992 | Common:3; Rare:64 | ||||
| chr12:123458086-123458205 | Common:1; Rare:29 | ||||
| chr12:123584317-123584593 | Common:6; Rare:85 | ||||
| chr12:123602022-123602174 | Common:3; Rare:56 | ||||
| chr12:123633558-123633852 | Common:1; Rare:141; Clinvar:8; Clinvar (benign):1 |