| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:102958202-102958629 | Common:5; Rare:153; Clinvar (benign):2 | ||||
| chr12:102958866-102959079 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr12:103930033-103930564 | Common:9; Rare:178 | ||||
| chr12:103957059-103957275 | Common:4; Rare:61 | ||||
| chr12:103965616-103965986 | Common:2; Rare:92 | ||||
| chr12:103966113-103966205 | Common:4; Rare:30 | ||||
| chr12:104064327-104064555 | Common:1; Rare:57 | ||||
| chr12:104138147-104138473 | Common:1; Rare:101 | ||||
| chr12:104286741-104287152 | Common:3; Rare:75 | ||||
| chr12:104287203-104287430 | Rare:59 | ||||
| chr12:104288720-104288951 | Common:1; Rare:94 | ||||
| chr12:104958247-104958430 | Common:3; Rare:54 | ||||
| chr12:104986190-104986365 | Common:2; Rare:63 | ||||
| chr12:105107588-105107789 | Common:1; Rare:89 | ||||
| chr12:105236035-105236364 | Common:3; Rare:146 |