| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123458294-123458540 | Common:3; Rare:59 | ||||
| chr12:123533036-123533436 | Common:2; Rare:125 | ||||
| chr12:123533951-123534243 | Common:3; Rare:87 | ||||
| chr12:123584283-123584593 | Common:6; Rare:95 | ||||
| chr12:123601779-123602176 | Common:6; Rare:109 | ||||
| chr12:123633633-123633940 | Common:2; Rare:134; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123670981-123671196 | Common:4; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:123712151-123712395 | Common:8; Rare:97; Clinvar (benign):2 | ||||
| chr12:123971530-123971920 | Common:1; Rare:98 | ||||
| chr12:123972561-123972778 | Common:4; Rare:67 | ||||
| chr12:123972850-123973290 | Common:2; Rare:129 | ||||
| chr12:123973714-123974301 | Common:6; Rare:201 | ||||
| chr12:124518615-124518759 | Rare:35 | ||||
| chr12:124567776-124568176 | Common:3; Rare:129 | ||||
| chr12:124786609-124786839 | Rare:54 |