| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120903490-120903532 | Rare:8 | ||||
| chr12:121352323-121352656 | Common:3; Rare:128 | ||||
| chr12:121399893-121400160 | Common:5; Rare:97 | ||||
| chr12:121580241-121580394 | Rare:53 | ||||
| chr12:121580962-121581110 | Rare:22 | ||||
| chr12:121712617-121712954 | Common:5; Rare:126 | ||||
| chr12:121802845-121803120 | Common:1; Rare:66 | ||||
| chr12:121803135-121803285 | Rare:38 | ||||
| chr12:121803925-121804041 | Rare:37 | ||||
| chr12:121888563-121888895 | Common:2; Rare:100 | ||||
| chr12:122021596-122022092 | Common:9; Rare:137 | ||||
| chr12:122266385-122266564 | Common:2; Rare:73 | ||||
| chr12:122278790-122279052 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr12:122500824-122501170 | Common:3; Rare:92 | ||||
| chr12:122513863-122514207 | Common:2; Rare:90 |