| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20684427-20684673 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20802796-20802970 | Common:1; Rare:23 | ||||
| chr14:20989665-20990036 | Common:7; Rare:92 | ||||
| chr14:21022062-21022277 | Rare:58 | ||||
| chr14:21024936-21025212 | Common:1; Rare:97 | ||||
| chr14:21025437-21026063 | Common:3; Rare:124 | ||||
| chr14:21383931-21384051 | Common:1; Rare:50 | ||||
| chr14:21456041-21456254 | Common:4; Rare:58 | ||||
| chr14:21476600-21476729 | Rare:62 | ||||
| chr14:21476868-21477262 | Common:2; Rare:124 | ||||
| chr14:21511284-21511557 | Rare:67 | ||||
| chr14:21526231-21526466 | Rare:50 | ||||
| chr14:22589144-22589479 | Common:4; Rare:108 | ||||
| chr14:22766543-22766756 | Common:1; Rare:123 | ||||
| chr14:22829781-22829940 | Common:1; Rare:59 |