| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31074053-31074271 | Common:1; Rare:49 | ||||
| chr12:31324134-31324457 | Common:1; Rare:68 | ||||
| chr12:31326093-31326439 | Common:4; Rare:120 | ||||
| chr12:31728813-31728972 | Common:2; Rare:36 | ||||
| chr12:31728993-31729313 | Common:1; Rare:103 | ||||
| chr12:31959176-31959241 | Common:1; Rare:10 | ||||
| chr12:31959249-31959477 | Common:2; Rare:73 | ||||
| chr12:32399858-32399870 | Rare:2 | ||||
| chr12:32679128-32679350 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:32755878-32756028 | Common:1; Rare:48 | ||||
| chr12:40224933-40225108 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:42144917-42144999 | Common:2; Rare:22 | ||||
| chr12:42326065-42326218 | Common:1; Rare:49 | ||||
| chr12:43758745-43759016 | Common:2; Rare:76; Clinvar:2 | ||||
| chr12:43806263-43806425 | Common:2; Rare:57 |