| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:112106627-112106767 | Rare:25 | ||||
| chr13:112895149-112895325 | Rare:48 | ||||
| chr13:114343945-114344242 | Common:2; Rare:59 | ||||
| chr14:28188816-28189011 | Common:6; Rare:49 | ||||
| chr14:40954283-40954739 | Common:5; Rare:156 | ||||
| chr14:47795004-47795180 | Common:1; Rare:66 | ||||
| chr14:47901624-47901808 | Common:2; Rare:56 | ||||
| chr14:49633949-49634070 | Common:1; Rare:50; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49862791-49863012 | Rare:91 | ||||
| chr14:57112665-57112809 | Common:1; Rare:35 | ||||
| chr14:59951858-59952149 | Common:3; Rare:53 | ||||
| chr14:68795244-68795425 | Common:3; Rare:40 | ||||
| chr14:69886142-69886243 | Rare:9 | ||||
| chr14:71848352-71848609 | Common:6; Rare:24 | ||||
| chr14:81170405-81170482 | Rare:18 |