| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120116705-120116917 | Common:1; Rare:64 | ||||
| chr12:120201072-120201360 | Common:2; Rare:92 | ||||
| chr12:120446235-120446477 | Common:1; Rare:86 | ||||
| chr12:120495923-120496144 | Common:4; Rare:60 | ||||
| chr12:121399885-121400147 | Common:5; Rare:94 | ||||
| chr12:121802939-121803070 | Rare:31 | ||||
| chr12:122526929-122527260 | Common:3; Rare:98 | ||||
| chr12:122974583-122974758 | Rare:41 | ||||
| chr12:123233087-123233490 | Common:2; Rare:134; Clinvar:1 | ||||
| chr12:123436452-123436762 | Common:1; Rare:67 | ||||
| chr12:123584334-123584589 | Common:5; Rare:70 | ||||
| chr12:123633553-123633845 | Common:1; Rare:139; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:125065303-125065450 | Common:2; Rare:56 | ||||
| chr12:128823981-128824092 | Rare:33 | ||||
| chr12:131710795-131711095 | Rare:80 |