| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49110048-49110374 | Common:2; Rare:72 | ||||
| chr12:49110553-49111107 | Rare:134 | ||||
| chr12:49129740-49129894 | Common:1; Rare:40 | ||||
| chr12:49130222-49130532 | Common:1; Rare:115 | ||||
| chr12:49130623-49131029 | Common:5; Rare:134 | ||||
| chr12:49131150-49131461 | Common:2; Rare:123 | ||||
| chr12:49131551-49131745 | Common:2; Rare:58 | ||||
| chr12:49131896-49132000 | Rare:18 | ||||
| chr12:49187930-49188005 | Rare:11 | ||||
| chr12:49188279-49188433 | Rare:43 | ||||
| chr12:49188486-49188867 | Common:3; Rare:71 | ||||
| chr12:49188871-49188972 | Common:2; Rare:27 | ||||
| chr12:49188985-49189307 | Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264376-49264901 | Common:7; Rare:126 | ||||
| chr12:49264918-49265348 | Common:1; Rare:151 |