| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526916-122527291 | Common:3; Rare:120 | ||||
| chr12:122974580-122974767 | Rare:45 | ||||
| chr12:122980538-122980986 | Common:2; Rare:133 | ||||
| chr12:123233087-123233494 | Common:2; Rare:137; Clinvar:1 | ||||
| chr12:123364816-123364952 | Common:1; Rare:51 | ||||
| chr12:123584334-123584739 | Common:7; Rare:137 | ||||
| chr12:123602030-123602139 | Common:3; Rare:34 | ||||
| chr12:123633620-123633851 | Common:1; Rare:108; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972580-123972869 | Common:6; Rare:103 | ||||
| chr12:124388781-124388978 | Common:3; Rare:65 | ||||
| chr12:124422528-124422808 | Common:4; Rare:80 | ||||
| chr12:130839155-130839386 | Common:2; Rare:85 | ||||
| chr12:130871735-130872110 | Common:4; Rare:156 | ||||
| chr12:131710795-131711110 | Rare:83 | ||||
| chr12:131929014-131929260 | Common:10; Rare:73 |