| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101739380-101739603 | Common:4; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:101877437-101877730 | Common:3; Rare:77 | ||||
| chr12:102120060-102120249 | Rare:73 | ||||
| chr12:102478497-102478610 | Rare:20 | ||||
| chr12:103587102-103587276 | Rare:46 | ||||
| chr12:103930072-103930509 | Common:8; Rare:150 | ||||
| chr12:103965730-103965960 | Common:2; Rare:51 | ||||
| chr12:104064341-104064598 | Common:1; Rare:61 | ||||
| chr12:104138153-104138448 | Common:1; Rare:87 | ||||
| chr12:105107641-105107795 | Common:1; Rare:74 | ||||
| chr12:105236065-105236271 | Common:2; Rare:95 | ||||
| chr12:106955520-106955923 | Rare:148 | ||||
| chr12:106987049-106987258 | Common:4; Rare:60 | ||||
| chr12:107093484-107093623 | Rare:52 | ||||
| chr12:108561141-108561448 | Common:3; Rare:74 |