| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110502047-110502210 | Common:1; Rare:60 | ||||
| chr12:110613811-110614162 | Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:110641601-110641853 | Common:1; Rare:48 | ||||
| chr12:110742825-110743171 | Common:3; Rare:134 | ||||
| chr12:111369011-111369277 | Common:1; Rare:72 | ||||
| chr12:111597384-111597425 | Rare:8 | ||||
| chr12:111597942-111598055 | Rare:38 | ||||
| chr12:111598785-111598838 | Rare:11 | ||||
| chr12:111599891-111600090 | Rare:47 | ||||
| chr12:111685752-111686133 | Rare:142 | ||||
| chr12:111766836-111767036 | Rare:65 | ||||
| chr12:111841877-111842260 | Common:3; Rare:107 | ||||
| chr12:111888585-111889005 | Common:1; Rare:84 | ||||
| chr12:112013096-112013523 | Common:1; Rare:162 | ||||
| chr12:112013533-112013594 | Rare:22 |