| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100986888-100987061 | Common:1; Rare:32 | ||||
| chr12:101280008-101280221 | Common:1; Rare:61 | ||||
| chr12:101407670-101408322 | Common:3; Rare:161 | ||||
| chr12:101697560-101697962 | Common:4; Rare:135 | ||||
| chr12:101698001-101698187 | Rare:64 | ||||
| chr12:101830732-101830848 | Common:2; Rare:39; Clinvar (benign):2 | ||||
| chr12:101830850-101830987 | Rare:65 | ||||
| chr12:101876885-101877078 | Common:3; Rare:43 | ||||
| chr12:101877121-101877346 | Common:4; Rare:42 | ||||
| chr12:101877390-101877769 | Common:4; Rare:100 | ||||
| chr12:102061651-102061669 | Rare:5 | ||||
| chr12:102061886-102062247 | Common:1; Rare:99 | ||||
| chr12:102120025-102120304 | Common:1; Rare:107 | ||||
| chr12:102120371-102120576 | Common:3; Rare:54 | ||||
| chr12:102415573-102415812 | Common:1; Rare:33 |