| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110502050-110502198 | Common:1; Rare:54 | ||||
| chr12:110641616-110641834 | Common:1; Rare:44 | ||||
| chr12:111597976-111598236 | Rare:79 | ||||
| chr12:111598792-111598825 | Rare:6 | ||||
| chr12:111685934-111686127 | Rare:66 | ||||
| chr12:111766823-111766980 | Rare:49 | ||||
| chr12:111841887-111842249 | Common:3; Rare:99 | ||||
| chr12:112013113-112013460 | Common:1; Rare:122 | ||||
| chr12:113185415-113185775 | Common:9; Rare:136 | ||||
| chr12:113221129-113221489 | Common:3; Rare:107 | ||||
| chr12:114407937-114408277 | Common:2; Rare:58; Clinvar (benign):4 | ||||
| chr12:116738064-116738319 | Common:3; Rare:78 | ||||
| chr12:118061055-118061464 | Common:4; Rare:90 | ||||
| chr12:118135953-118136264 | Common:2; Rare:90 | ||||
| chr12:118372846-118373189 | Common:2; Rare:93 |