| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93377728-93377970 | Rare:80 | ||||
| chr12:93378163-93378419 | Common:1; Rare:61 | ||||
| chr12:93570827-93571085 | Rare:66 | ||||
| chr12:93571738-93571902 | Common:6; Rare:63 | ||||
| chr12:94459833-94460000 | Common:2; Rare:47 | ||||
| chr12:95217384-95217746 | Common:4; Rare:99 | ||||
| chr12:98515353-98515876 | Common:1; Rare:189; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98593484-98593854 | Common:2; Rare:116; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644738-98645296 | Common:5; Rare:162 | ||||
| chr12:100142839-100143157 | Common:3; Rare:102 | ||||
| chr12:100267049-100267280 | Common:1; Rare:112 | ||||
| chr12:101407711-101408056 | Common:3; Rare:84 | ||||
| chr12:101877532-101877746 | Common:3; Rare:58 | ||||
| chr12:102120065-102120210 | Rare:54 | ||||
| chr12:103841259-103841466 | Common:3; Rare:67 |