| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:32201706-32201739 | Rare:9 | ||||
| chr14:32203248-32203646 | Common:13; Rare:176 | ||||
| chr14:32418050-32418420 | Common:1; Rare:59 | ||||
| chr14:49633956-49634053 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49862655-49862994 | Common:1; Rare:160 | ||||
| chr14:54568913-54569051 | Common:1; Rare:25 | ||||
| chr14:54569502-54569601 | Rare:22 | ||||
| chr14:61750979-61751232 | Rare:68 | ||||
| chr14:71001873-71002075 | Common:1; Rare:36 | ||||
| chr14:72894956-72895091 | Rare:20 | ||||
| chr14:73633757-73633862 | Common:3; Rare:19 | ||||
| chr14:75258976-75259309 | Common:2; Rare:83 | ||||
| chr14:75294104-75294458 | Common:2; Rare:90 | ||||
| chr14:77032859-77033090 | Common:2; Rare:50 | ||||
| chr14:77033265-77033508 | Common:7; Rare:54 |