| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49688199-49688278 | Rare:29 | ||||
| chr14:49693046-49693167 | Common:1; Rare:39 | ||||
| chr14:49767506-49767704 | Common:2; Rare:76 | ||||
| chr14:49852713-49852886 | Common:2; Rare:72 | ||||
| chr14:49853019-49853149 | Rare:26 | ||||
| chr14:49892909-49893125 | Rare:87 | ||||
| chr14:50116553-50116668 | Rare:57 | ||||
| chr14:50312093-50312376 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:50532467-50532798 | Common:3; Rare:103 | ||||
| chr14:50668322-50668556 | Common:3; Rare:86 | ||||
| chr14:50944378-50944583 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51095118-51095298 | Common:3; Rare:73 | ||||
| chr14:51240093-51240295 | Common:1; Rare:81 | ||||
| chr14:51651636-51651984 | Common:4; Rare:100 | ||||
| chr14:51989349-51989700 | Common:2; Rare:111 |