| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118061037-118061407 | Common:3; Rare:85 | ||||
| chr12:118103816-118104122 | Common:1; Rare:74 | ||||
| chr12:118135917-118136367 | Common:2; Rare:132 | ||||
| chr12:118139216-118139544 | Common:2; Rare:71 | ||||
| chr12:118372846-118373165 | Common:2; Rare:83 | ||||
| chr12:118376370-118376561 | Common:1; Rare:50 | ||||
| chr12:119668094-119668184 | Common:1; Rare:18 | ||||
| chr12:120116655-120116946 | Common:5; Rare:89 | ||||
| chr12:120194678-120194814 | Common:1; Rare:53 | ||||
| chr12:120201081-120201385 | Common:2; Rare:96 | ||||
| chr12:120437892-120438229 | Common:2; Rare:129; Clinvar (benign):2 | ||||
| chr12:120446329-120446478 | Common:1; Rare:66 | ||||
| chr12:120469618-120470006 | Common:3; Rare:123 | ||||
| chr12:120495843-120496266 | Common:8; Rare:142 | ||||
| chr12:120581334-120581577 | Common:1; Rare:84 |