| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122422574-122422837 | Common:4; Rare:86 | ||||
| chr12:122526864-122527291 | Common:4; Rare:152 | ||||
| chr12:122752467-122752921 | Common:1; Rare:146 | ||||
| chr12:122896058-122896272 | Rare:101 | ||||
| chr12:122975143-122975252 | Common:1; Rare:32 | ||||
| chr12:122980196-122980292 | Rare:34 | ||||
| chr12:122980558-122980969 | Common:2; Rare:120 | ||||
| chr12:123233081-123233504 | Common:3; Rare:145; Clinvar:1 | ||||
| chr12:123364825-123364983 | Common:3; Rare:58 | ||||
| chr12:123383950-123384188 | Rare:60 | ||||
| chr12:123584314-123584816 | Common:9; Rare:167 | ||||
| chr12:123633597-123633851 | Common:1; Rare:123; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972540-123972893 | Common:6; Rare:120 | ||||
| chr12:124422636-124422816 | Common:2; Rare:45 | ||||
| chr12:124914877-124915057 | Common:3; Rare:86 |