| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:119667934-119668117 | Common:1; Rare:47 | ||||
| chr12:120116759-120116935 | Common:2; Rare:60 | ||||
| chr12:120194683-120194786 | Rare:37 | ||||
| chr12:120201081-120201374 | Common:2; Rare:93 | ||||
| chr12:120437842-120438229 | Common:2; Rare:143; Clinvar (benign):2 | ||||
| chr12:120446292-120446735 | Common:4; Rare:176 | ||||
| chr12:120469535-120469912 | Common:3; Rare:130 | ||||
| chr12:120495831-120496214 | Common:8; Rare:129 | ||||
| chr12:120534308-120534371 | Rare:24 | ||||
| chr12:121221978-121222136 | Common:3; Rare:69 | ||||
| chr12:121580241-121580507 | Rare:79 | ||||
| chr12:121802931-121803091 | Rare:40 | ||||
| chr12:121803148-121803310 | Rare:45 | ||||
| chr12:121858685-121859035 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:122266396-122266518 | Common:1; Rare:59 |