| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:21102054-21102454 | Common:3; Rare:99 | ||||
| chr14:21102474-21102874 | Rare:99 | ||||
| chr14:21103570-21104280 | Common:22; Rare:688 | ||||
| chr14:21104297-21104450 | Common:3; Rare:27 | ||||
| chr14:21104390-21104632 | Common:6; Rare:92 | ||||
| chr14:21104544-21104944 | Common:7; Rare:95 | ||||
| chr14:21233990-21234450 | Common:3; Rare:97 | ||||
| chr14:21267692-21268459 | Common:4; Rare:375 | ||||
| chr14:21268437-21269425 | Common:1; Rare:668 | ||||
| chr14:21269392-21270016 | Common:21; Rare:901 | ||||
| chr14:21317441-21317873 | Common:4; Rare:289; Clinvar:4; Clinvar (benign):2 | ||||
| chr14:21319890-21320568 | Common:5; Rare:292; Clinvar:4 | ||||
| chr14:21383394-21383596 | Common:2; Rare:53 | ||||
| chr14:21383542-21384537 | Common:27; Rare:1408 | ||||
| chr14:21384528-21384928 | Common:1; Rare:93 |