| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51239130-51239306 | Common:2; Rare:51 | ||||
| chr12:51270274-51270418 | Common:3; Rare:40 | ||||
| chr12:51391592-51391737 | Common:1; Rare:43 | ||||
| chr12:52051139-52051451 | Common:1; Rare:101 | ||||
| chr12:52232605-52232771 | Rare:33 | ||||
| chr12:52233075-52233530 | Common:5; Rare:152 | ||||
| chr12:52248815-52249057 | Rare:37 | ||||
| chr12:52904764-52905347 | Common:7; Rare:170; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:52926440-52926580 | Rare:37 | ||||
| chr12:52948787-52949305 | Common:2; Rare:146; Clinvar:1 | ||||
| chr12:52949774-52950066 | Rare:62 | ||||
| chr12:52951496-52951856 | Rare:95; Clinvar:5 | ||||
| chr12:53006117-53006486 | Common:4; Rare:134 | ||||
| chr12:53079329-53079559 | Common:2; Rare:78 | ||||
| chr12:53097565-53097687 | Rare:38 |