| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109880337-109880664 | Common:1; Rare:101 | ||||
| chr12:109996313-109996633 | Common:3; Rare:77 | ||||
| chr12:110468522-110468915 | Rare:106 | ||||
| chr12:110502058-110502195 | Common:1; Rare:51 | ||||
| chr12:110614011-110614212 | Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685761-111686110 | Rare:130 | ||||
| chr12:111766767-111766984 | Rare:64 | ||||
| chr12:111841887-111842233 | Common:3; Rare:93 | ||||
| chr12:112013123-112013573 | Common:1; Rare:170 | ||||
| chr12:112108741-112108820 | Rare:26 | ||||
| chr12:113185429-113185794 | Common:9; Rare:132 | ||||
| chr12:113221005-113221322 | Common:2; Rare:93 | ||||
| chr12:113966288-113966462 | Common:3; Rare:56 | ||||
| chr12:114683879-114684353 | Common:4; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:114684518-114684737 | Common:2; Rare:62 |