| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20989691-20990011 | Common:7; Rare:71 | ||||
| chr14:21103746-21104098 | Common:3; Rare:85 | ||||
| chr14:21383931-21384425 | Common:8; Rare:173 | ||||
| chr14:21437221-21437406 | Common:4; Rare:77 | ||||
| chr14:21456041-21456221 | Common:3; Rare:48 | ||||
| chr14:21476843-21477267 | Common:2; Rare:139 | ||||
| chr14:21511289-21511534 | Rare:64 | ||||
| chr14:22766537-22766710 | Common:1; Rare:87 | ||||
| chr14:22815808-22815915 | Rare:19; Clinvar (benign):1 | ||||
| chr14:22819740-22819879 | Common:3; Rare:28; Clinvar (benign):1 | ||||
| chr14:22829778-22829924 | Rare:54 | ||||
| chr14:22871644-22871797 | Rare:43 | ||||
| chr14:22919077-22919491 | Common:8; Rare:114 | ||||
| chr14:22929340-22929643 | Common:1; Rare:87 | ||||
| chr14:22957021-22957194 | Rare:51 |