| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69611450-69611802 | Common:2; Rare:116 | ||||
| chr14:69767676-69767980 | Common:1; Rare:129 | ||||
| chr14:70080174-70080296 | Common:1; Rare:24 | ||||
| chr14:70188924-70189124 | Common:3; Rare:40 | ||||
| chr14:70416968-70417125 | Rare:50 | ||||
| chr14:70641181-70641392 | Common:3; Rare:34 | ||||
| chr14:70907782-70907906 | Common:3; Rare:51 | ||||
| chr14:71320308-71320518 | Rare:64 | ||||
| chr14:72926164-72926524 | Common:6; Rare:90 | ||||
| chr14:73058301-73058661 | Common:3; Rare:110 | ||||
| chr14:73058760-73058870 | Common:1; Rare:27 | ||||
| chr14:73136331-73136553 | Common:4; Rare:75; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73458504-73458849 | Common:5; Rare:88 | ||||
| chr14:73644819-73645042 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73714316-73714534 | Common:2; Rare:82 |