| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120194683-120194804 | Rare:45 | ||||
| chr12:120201081-120201360 | Common:2; Rare:89 | ||||
| chr12:120437896-120438229 | Common:2; Rare:128; Clinvar (benign):2 | ||||
| chr12:120446338-120446495 | Common:2; Rare:72 | ||||
| chr12:120469496-120469906 | Common:5; Rare:139 | ||||
| chr12:120495845-120496228 | Common:7; Rare:128 | ||||
| chr12:120529127-120529188 | Common:1; Rare:21 | ||||
| chr12:120687373-120687467 | Rare:30 | ||||
| chr12:121209887-121210146 | Common:5; Rare:77 | ||||
| chr12:121581003-121581143 | Rare:21 | ||||
| chr12:121712611-121712844 | Common:5; Rare:94 | ||||
| chr12:121802931-121803109 | Common:1; Rare:45 | ||||
| chr12:121888626-121888876 | Common:2; Rare:81 | ||||
| chr12:121918467-121918609 | Common:4; Rare:28 | ||||
| chr12:122266408-122266573 | Common:2; Rare:64 |