| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101830800-101831150 | Common:2; Rare:113; Clinvar (benign):2 | ||||
| chr12:101877424-101877593 | Common:1; Rare:39 | ||||
| chr12:102061924-102062225 | Common:1; Rare:81 | ||||
| chr12:102120038-102120239 | Rare:78 | ||||
| chr12:102120446-102120557 | Common:1; Rare:34 | ||||
| chr12:102957453-102957690 | Common:4; Rare:58 | ||||
| chr12:102958567-102958967 | Common:2; Rare:132; Clinvar (benign):2 | ||||
| chr12:103495879-103496107 | Common:5; Rare:49 | ||||
| chr12:103841214-103841490 | Common:4; Rare:103 | ||||
| chr12:103930120-103930490 | Common:8; Rare:127 | ||||
| chr12:103930779-103930967 | Common:3; Rare:46 | ||||
| chr12:103957113-103957401 | Common:9; Rare:75 | ||||
| chr12:103965624-103965931 | Common:2; Rare:83 | ||||
| chr12:103966113-103966213 | Common:4; Rare:32 | ||||
| chr12:104049930-104050380 | Common:1; Rare:76 |