| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121803893-121804074 | Rare:54 | ||||
| chr12:121858809-121859056 | Common:4; Rare:98; Clinvar (benign):4 | ||||
| chr12:121888620-121888901 | Common:4; Rare:172 | ||||
| chr12:122021822-122022031 | Common:18; Rare:106 | ||||
| chr12:122078467-122078809 | Common:6; Rare:205 | ||||
| chr12:122266389-122266573 | Common:4; Rare:135 | ||||
| chr12:122422429-122422718 | Common:2; Rare:121 | ||||
| chr12:122422717-122423033 | Common:3; Rare:95 | ||||
| chr12:122500841-122501170 | Common:3; Rare:89 | ||||
| chr12:122526881-122527331 | Common:7; Rare:290 | ||||
| chr12:122896064-122896256 | Rare:96 | ||||
| chr12:122974533-122974841 | Common:1; Rare:132 | ||||
| chr12:122975139-122975339 | Common:2; Rare:158 | ||||
| chr12:122980162-122980292 | Rare:79 | ||||
| chr12:122980565-122980969 | Common:4; Rare:234 |