| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121889023-121889134 | Rare:29 | ||||
| chr12:121918408-121918606 | Common:5; Rare:44 | ||||
| chr12:122021797-122021980 | Common:9; Rare:55 | ||||
| chr12:122078593-122078870 | Common:3; Rare:96 | ||||
| chr12:122225736-122225844 | Rare:34 | ||||
| chr12:122225896-122226496 | Common:3; Rare:284; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:122266009-122266099 | Common:1; Rare:25 | ||||
| chr12:122266297-122266651 | Common:2; Rare:120 | ||||
| chr12:122266993-122267069 | Rare:11 | ||||
| chr12:122422179-122422531 | Rare:98 | ||||
| chr12:122500177-122500459 | Common:2; Rare:53 | ||||
| chr12:122500739-122501009 | Rare:84 | ||||
| chr12:122526867-122527346 | Common:4; Rare:172 | ||||
| chr12:122527694-122527799 | Common:1; Rare:24 | ||||
| chr12:122752485-122752924 | Common:1; Rare:142 |