| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118372617-118373220 | Common:3; Rare:152 | ||||
| chr12:119668094-119668224 | Common:1; Rare:31 | ||||
| chr12:120116715-120116926 | Common:2; Rare:69 | ||||
| chr12:120194659-120194803 | Rare:52 | ||||
| chr12:120201077-120201369 | Common:2; Rare:92 | ||||
| chr12:120437900-120438123 | Common:2; Rare:66; Clinvar (benign):1 | ||||
| chr12:120446282-120446508 | Common:2; Rare:91 | ||||
| chr12:120495935-120496144 | Common:4; Rare:56 | ||||
| chr12:120686967-120687184 | Common:1; Rare:74 | ||||
| chr12:121209901-121210065 | Common:3; Rare:44 | ||||
| chr12:121399895-121400147 | Common:5; Rare:91 | ||||
| chr12:121580227-121580360 | Rare:41 | ||||
| chr12:121888635-121888859 | Common:2; Rare:73 | ||||
| chr12:122021859-122022025 | Common:8; Rare:45 | ||||
| chr12:122500832-122501170 | Common:3; Rare:90 |