| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101407686-101408035 | Common:3; Rare:79 | ||||
| chr12:102120060-102120249 | Rare:73 | ||||
| chr12:103930030-103930564 | Common:9; Rare:178 | ||||
| chr12:103965717-103965960 | Common:2; Rare:52 | ||||
| chr12:104064465-104064555 | Rare:26 | ||||
| chr12:104138147-104138390 | Common:1; Rare:61 | ||||
| chr12:104288773-104288947 | Rare:81 | ||||
| chr12:105107612-105107803 | Common:1; Rare:91; Clinvar:1 | ||||
| chr12:105236035-105236304 | Common:2; Rare:116 | ||||
| chr12:106774509-106774618 | Rare:22 | ||||
| chr12:107093490-107093599 | Rare:44 | ||||
| chr12:107685706-107685895 | Rare:67 | ||||
| chr12:107761036-107761360 | Common:6; Rare:123 | ||||
| chr12:108562417-108562705 | Common:9; Rare:120; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109052465-109052667 | Common:3; Rare:62 |