| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69398586-69398756 | Rare:39 | ||||
| chr14:69611462-69611698 | Common:1; Rare:83 | ||||
| chr14:69767683-69767956 | Common:1; Rare:119 | ||||
| chr14:70416968-70417154 | Rare:57 | ||||
| chr14:70600620-70600953 | Common:3; Rare:81 | ||||
| chr14:70809514-70809956 | Common:4; Rare:124 | ||||
| chr14:70907293-70907568 | Common:2; Rare:112 | ||||
| chr14:71320201-71320510 | Rare:99 | ||||
| chr14:72926202-72926528 | Common:4; Rare:77 | ||||
| chr14:73027058-73027227 | Common:1; Rare:47 | ||||
| chr14:73058295-73058701 | Common:3; Rare:121 | ||||
| chr14:73058751-73058861 | Common:1; Rare:26 | ||||
| chr14:73136361-73136558 | Common:4; Rare:70; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73458520-73458894 | Common:5; Rare:98 | ||||
| chr14:73567946-73568128 | Rare:51 |