| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130069659-130069946 | Common:2; Rare:99 | ||||
| chr11:134253314-134253594 | Common:2; Rare:91; Clinvar (benign):1 | ||||
| chr12:389300-389383 | Rare:31 | ||||
| chr12:991101-991251 | Common:1; Rare:56 | ||||
| chr12:2812534-2812715 | Common:1; Rare:46 | ||||
| chr12:2877027-2877262 | Rare:70 | ||||
| chr12:3753064-3753252 | Common:1; Rare:45 | ||||
| chr12:4538439-4538933 | Common:3; Rare:111 | ||||
| chr12:4648982-4649149 | Common:2; Rare:54; Clinvar (benign):1 | ||||
| chr12:5431936-5432118 | Common:4; Rare:73 | ||||
| chr12:6383993-6384268 | Common:1; Rare:61 | ||||
| chr12:6452031-6452134 | Common:1; Rare:23 | ||||
| chr12:6493219-6493387 | Common:6; Rare:46 | ||||
| chr12:6493840-6494132 | Common:2; Rare:87 | ||||
| chr12:6534240-6534582 | Common:6; Rare:135 |