| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53181313-53181408 | Rare:26 | ||||
| chr12:53252031-53252192 | Common:3; Rare:66 | ||||
| chr12:53501188-53501357 | Rare:39 | ||||
| chr12:53501537-53501596 | Rare:11 | ||||
| chr12:53625951-53626127 | Common:1; Rare:40 | ||||
| chr12:53999962-54000126 | Common:4; Rare:43 | ||||
| chr12:54259517-54259727 | Rare:40 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:55707503-55707597 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55716008-55716208 | Common:1; Rare:91 | ||||
| chr12:55725869-55726190 | Rare:65 | ||||
| chr12:55728952-55729135 | Rare:33 | ||||
| chr12:55729661-55729797 | Rare:31 | ||||
| chr12:55829511-55829793 | Rare:92 | ||||
| chr12:55830732-55830947 | Rare:67 |