| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20343174-20343647 | Common:12; Rare:277 | ||||
| chr14:20454772-20455270 | Common:7; Rare:131 | ||||
| chr14:20456391-20456705 | Common:1; Rare:81; Clinvar:1 | ||||
| chr14:20461424-20461715 | Common:1; Rare:76 | ||||
| chr14:20684429-20684745 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:20802788-20802970 | Common:1; Rare:24 | ||||
| chr14:21024220-21024316 | Rare:20 | ||||
| chr14:21025015-21025345 | Rare:102 | ||||
| chr14:21476868-21477267 | Common:2; Rare:128 | ||||
| chr14:22589144-22589328 | Common:4; Rare:64 | ||||
| chr14:22766591-22766699 | Common:1; Rare:59 | ||||
| chr14:22829781-22829915 | Rare:46 | ||||
| chr14:22872058-22872222 | Common:2; Rare:38 | ||||
| chr14:22929363-22929613 | Rare:58 | ||||
| chr14:22982614-22982932 | Common:3; Rare:108 |