| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113422276-113422491 | Common:6; Rare:115 | ||||
| chr12:113966233-113966566 | Common:27; Rare:273 | ||||
| chr12:114683142-114683467 | Common:3; Rare:86; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:114683888-114684831 | Common:15; Rare:583; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:116276672-116276907 | Common:2; Rare:104 | ||||
| chr12:116277177-116277936 | Common:6; Rare:482 | ||||
| chr12:116737207-116737807 | Common:37; Rare:316 | ||||
| chr12:116737938-116738400 | Common:16; Rare:417 | ||||
| chr12:116878589-116878719 | Common:2; Rare:29 | ||||
| chr12:116878730-116879170 | Common:3; Rare:132 | ||||
| chr12:116881010-116881132 | Common:1; Rare:30 | ||||
| chr12:116881389-116881594 | Common:5; Rare:76 | ||||
| chr12:116910814-116911068 | Common:1; Rare:151 | ||||
| chr12:117190346-117190640 | Common:1; Rare:199 | ||||
| chr12:117968752-117969580 | Common:14; Rare:570 |