| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24213095-24213186 | Rare:16 | ||||
| chr14:24213435-24213539 | Rare:38 | ||||
| chr14:24213556-24213598 | Common:1; Rare:10 | ||||
| chr14:24232289-24232681 | Common:8; Rare:102 | ||||
| chr14:24232816-24232934 | Common:1; Rare:26 | ||||
| chr14:24242604-24242741 | Rare:26; Clinvar:1 | ||||
| chr14:24271460-24271604 | Common:1; Rare:41 | ||||
| chr14:24299749-24299854 | Common:1; Rare:30 | ||||
| chr14:24442677-24443023 | Common:5; Rare:110 | ||||
| chr14:30622194-30622362 | Common:1; Rare:70 | ||||
| chr14:31207633-31207911 | Common:2; Rare:97 | ||||
| chr14:31420528-31420763 | Common:3; Rare:71 | ||||
| chr14:31457369-31457577 | Common:2; Rare:73 | ||||
| chr14:31561383-31561498 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076598-32077026 | Common:3; Rare:123 |