| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121802670-121805165 | Common:7; Rare:2007 | ||||
| chr12:121805071-121805568 | Common:4; Rare:202 | ||||
| chr12:121888470-121888917 | Common:13; Rare:553 | ||||
| chr12:121889044-121889207 | Rare:56 | ||||
| chr12:121889190-121889590 | Rare:92 | ||||
| chr12:121893100-121893590 | Common:7; Rare:152 | ||||
| chr12:121933680-121934339 | Common:12; Rare:395; Clinvar (benign):3 | ||||
| chr12:121934325-121934725 | Common:2; Rare:67 | ||||
| chr12:122021456-122021856 | Common:1; Rare:111 | ||||
| chr12:122021814-122022023 | Common:36; Rare:213 | ||||
| chr12:122021979-122023042 | Common:6; Rare:514 | ||||
| chr12:122078370-122079100 | Common:26; Rare:933 | ||||
| chr12:122203201-122203892 | Common:4; Rare:555 | ||||
| chr12:122225204-122226024 | Common:4; Rare:470; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:122225926-122226484 | Common:5; Rare:633; Clinvar:7; Clinvar (benign):3 |