| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50764718-50764898 | Common:2; Rare:47 | ||||
| chr12:50924280-50924419 | Rare:17 | ||||
| chr12:50924456-50924675 | Common:3; Rare:67 | ||||
| chr12:50924868-50925021 | Common:1; Rare:32 | ||||
| chr12:51025770-51025902 | Common:1; Rare:27 | ||||
| chr12:51026300-51026618 | Common:6; Rare:122; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51028214-51028334 | Rare:30 | ||||
| chr12:51047838-51048007 | Common:2; Rare:30 | ||||
| chr12:51048039-51048395 | Common:2; Rare:119 | ||||
| chr12:51082938-51083051 | Rare:23 | ||||
| chr12:51083433-51083861 | Common:1; Rare:154 | ||||
| chr12:51172676-51172794 | Common:1; Rare:21 | ||||
| chr12:51172813-51172887 | Common:2; Rare:15 | ||||
| chr12:51172994-51173336 | Rare:72 | ||||
| chr12:51217208-51217296 | Rare:14 |