| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:70591928-70591951 | Rare:4 | ||||
| chr14:70907312-70907601 | Common:2; Rare:111 | ||||
| chr14:71320289-71320508 | Rare:69 | ||||
| chr14:71321026-71321173 | Common:1; Rare:53 | ||||
| chr14:72893963-72894264 | Common:4; Rare:95 | ||||
| chr14:72926185-72926529 | Common:6; Rare:83 | ||||
| chr14:73026961-73027208 | Common:1; Rare:60 | ||||
| chr14:73058309-73058627 | Common:3; Rare:98 | ||||
| chr14:73490801-73491007 | Common:4; Rare:68 | ||||
| chr14:73569026-73569075 | Rare:4 | ||||
| chr14:73644883-73645046 | Common:3; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73714360-73714553 | Common:2; Rare:67 | ||||
| chr14:73787115-73787383 | Common:2; Rare:94 | ||||
| chr14:73851746-73851983 | Common:4; Rare:83 | ||||
| chr14:73949979-73950372 | Common:7; Rare:171; Clinvar (benign):5 |