| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24195431-24195727 | Common:1; Rare:69 | ||||
| chr14:24216047-24216142 | Rare:23 | ||||
| chr14:24232317-24232650 | Common:8; Rare:79 | ||||
| chr14:24232848-24232936 | Rare:21 | ||||
| chr14:24242580-24242725 | Common:1; Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24299749-24299854 | Common:1; Rare:30 | ||||
| chr14:24442666-24443013 | Common:5; Rare:112 | ||||
| chr14:26597392-26597628 | Common:1; Rare:45 | ||||
| chr14:26597629-26597754 | Rare:30 | ||||
| chr14:28765284-28765402 | Rare:16 | ||||
| chr14:28765473-28765733 | Common:1; Rare:49 | ||||
| chr14:30559083-30559201 | Common:1; Rare:41 | ||||
| chr14:30622194-30622344 | Rare:54 | ||||
| chr14:31025366-31025675 | Common:2; Rare:75 | ||||
| chr14:31207655-31207911 | Common:2; Rare:92 |