| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121804660-121805333 | Common:1; Rare:234 | ||||
| chr12:121888523-121888972 | Common:8; Rare:327 | ||||
| chr12:121893247-121894242 | Common:2; Rare:260 | ||||
| chr12:121918380-121918660 | Common:11; Rare:101 | ||||
| chr12:122021278-122021678 | Rare:129 | ||||
| chr12:122021762-122022207 | Common:28; Rare:317 | ||||
| chr12:122078452-122078872 | Common:8; Rare:329 | ||||
| chr12:122203220-122203580 | Rare:330 | ||||
| chr12:122203588-122203768 | Common:3; Rare:158 | ||||
| chr12:122225717-122226069 | Rare:243; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:122265780-122266122 | Common:2; Rare:114 | ||||
| chr12:122266375-122266659 | Common:6; Rare:236 | ||||
| chr12:122399910-122400210 | Rare:91 | ||||
| chr12:122400494-122400759 | Common:1; Rare:45 | ||||
| chr12:122422370-122422890 | Common:8; Rare:272 |