| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109999085-109999462 | Rare:87 | ||||
| chr12:110281073-110281344 | Rare:97; Clinvar (benign):1 | ||||
| chr12:110450271-110450443 | Common:2; Rare:60 | ||||
| chr12:110468662-110468911 | Rare:64 | ||||
| chr12:110502053-110502236 | Common:1; Rare:64 | ||||
| chr12:111598792-111598926 | Rare:37; Clinvar (pathogenic):1 | ||||
| chr12:111599278-111599490 | Common:2; Rare:75 | ||||
| chr12:111685933-111686119 | Rare:62 | ||||
| chr12:111841887-111842263 | Common:3; Rare:106 | ||||
| chr12:112013093-112013475 | Common:1; Rare:135 | ||||
| chr12:112108741-112108961 | Common:1; Rare:60 | ||||
| chr12:113185436-113185777 | Common:8; Rare:123 | ||||
| chr12:114407983-114408282 | Common:2; Rare:54; Clinvar (benign):4 | ||||
| chr12:116738028-116738338 | Common:4; Rare:98 | ||||
| chr12:118061046-118061283 | Common:1; Rare:68 |