| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122974590-122974817 | Rare:46 | ||||
| chr12:122975143-122975252 | Common:1; Rare:32 | ||||
| chr12:122980171-122980256 | Rare:30 | ||||
| chr12:122980559-122980915 | Common:2; Rare:107 | ||||
| chr12:123232753-123232919 | Common:4; Rare:44 | ||||
| chr12:123233081-123233517 | Common:3; Rare:151; Clinvar:1 | ||||
| chr12:123269517-123269857 | Common:1; Rare:99 | ||||
| chr12:123272227-123272559 | Rare:77 | ||||
| chr12:123364758-123364989 | Common:5; Rare:100 | ||||
| chr12:123383785-123384189 | Rare:88 | ||||
| chr12:123436437-123436546 | Rare:16 | ||||
| chr12:123458085-123458229 | Common:1; Rare:36 | ||||
| chr12:123584307-123584669 | Common:8; Rare:129 | ||||
| chr12:123602010-123602190 | Common:3; Rare:62 | ||||
| chr12:123633544-123633877 | Common:2; Rare:157; Clinvar:8; Clinvar (benign):1 |