| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110613991-110614203 | Rare:64; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685730-111686090 | Rare:132 | ||||
| chr12:111766823-111767040 | Rare:69 | ||||
| chr12:111841898-111842243 | Common:3; Rare:94 | ||||
| chr12:112013123-112013468 | Common:1; Rare:122 | ||||
| chr12:112419077-112419118 | Rare:10; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:112938284-112938512 | Common:1; Rare:46 | ||||
| chr12:113185429-113185777 | Common:9; Rare:129 | ||||
| chr12:113221038-113221319 | Common:2; Rare:80 | ||||
| chr12:113403881-113403906 | Rare:5 | ||||
| chr12:113966298-113966527 | Common:8; Rare:79 | ||||
| chr12:114405788-114405885 | Common:1; Rare:15 | ||||
| chr12:114408051-114408219 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr12:114408616-114408999 | Rare:78 | ||||
| chr12:118103882-118104128 | Common:1; Rare:59 |