| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122001400-122001710 | Common:1; Rare:88 | ||||
| chr12:122021650-122022200 | Common:10; Rare:157 | ||||
| chr12:122078525-122078771 | Common:2; Rare:72 | ||||
| chr12:122225447-122225847 | Common:1; Rare:152 | ||||
| chr12:122225964-122226268 | Common:1; Rare:176; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:122266377-122266657 | Common:2; Rare:98 | ||||
| chr12:122421963-122422229 | Rare:68 | ||||
| chr12:122422954-122423106 | Rare:27 | ||||
| chr12:122500922-122501160 | Common:3; Rare:58 | ||||
| chr12:122526883-122527296 | Common:4; Rare:145 | ||||
| chr12:122752603-122752906 | Common:1; Rare:111 | ||||
| chr12:122753043-122753464 | Rare:135 | ||||
| chr12:122835349-122835511 | Rare:36 | ||||
| chr12:122871970-122872580 | Common:2; Rare:103 | ||||
| chr12:122896077-122896224 | Rare:80 |