| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20684414-20684531 | Common:1; Rare:15; Clinvar (benign):1 | ||||
| chr14:20989614-20990097 | Common:8; Rare:130 | ||||
| chr14:20990332-20990482 | Common:1; Rare:57 | ||||
| chr14:21025051-21025200 | Rare:54 | ||||
| chr14:21069619-21069838 | Common:2; Rare:50 | ||||
| chr14:21071050-21071073 | Rare:7 | ||||
| chr14:21071082-21071160 | Rare:13 | ||||
| chr14:21071265-21071930 | Common:5; Rare:136 | ||||
| chr14:21094471-21094654 | Rare:22 | ||||
| chr14:21098081-21098321 | Rare:40 | ||||
| chr14:21098481-21098797 | Common:1; Rare:69 | ||||
| chr14:21098816-21098883 | Rare:15 | ||||
| chr14:21103692-21103834 | Rare:34 | ||||
| chr14:21103847-21104254 | Common:5; Rare:99 | ||||
| chr14:21104258-21104391 | Common:2; Rare:25 |