| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120437926-120438223 | Common:2; Rare:116; Clinvar (benign):2 | ||||
| chr12:120446229-120446504 | Common:2; Rare:104 | ||||
| chr12:120469456-120469872 | Common:5; Rare:137 | ||||
| chr12:120495845-120496214 | Common:7; Rare:127 | ||||
| chr12:120534312-120534399 | Rare:37 | ||||
| chr12:120565105-120565528 | Common:1; Rare:113 | ||||
| chr12:120686967-120687247 | Common:2; Rare:90 | ||||
| chr12:120687310-120687441 | Common:1; Rare:42 | ||||
| chr12:121296659-121296914 | Common:1; Rare:76 | ||||
| chr12:121352325-121352620 | Common:3; Rare:111 | ||||
| chr12:121399885-121400166 | Common:5; Rare:104 | ||||
| chr12:121580226-121580368 | Rare:47 | ||||
| chr12:121580971-121581098 | Rare:15 | ||||
| chr12:121672608-121672680 | Common:4; Rare:29 | ||||
| chr12:121802849-121803117 | Common:1; Rare:64 |