| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107685709-107685834 | Rare:42 | ||||
| chr12:108731512-108731697 | Common:2; Rare:68 | ||||
| chr12:109097991-109098229 | Common:4; Rare:79 | ||||
| chr12:109477287-109477649 | Common:3; Rare:88 | ||||
| chr12:109573472-109573813 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:110502058-110502242 | Common:1; Rare:65 | ||||
| chr12:111685752-111686085 | Rare:125 | ||||
| chr12:112013129-112013460 | Common:1; Rare:114 | ||||
| chr12:113185435-113185748 | Common:7; Rare:118 | ||||
| chr12:113966315-113966513 | Common:7; Rare:70 | ||||
| chr12:118135955-118136175 | Common:2; Rare:69 | ||||
| chr12:118372868-118373129 | Common:1; Rare:66 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120446353-120446474 | Common:1; Rare:55 | ||||
| chr12:120469543-120469895 | Common:3; Rare:122 |