| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20454789-20455270 | Common:7; Rare:126 | ||||
| chr14:20684461-20684756 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20999056-20999305 | Rare:50 | ||||
| chr14:21022100-21022427 | Rare:80 | ||||
| chr14:21025670-21025803 | Rare:28 | ||||
| chr14:21383923-21384105 | Common:6; Rare:69 | ||||
| chr14:21437221-21437416 | Common:4; Rare:79 | ||||
| chr14:21456042-21456311 | Common:4; Rare:68 | ||||
| chr14:21476599-21476759 | Rare:70 | ||||
| chr14:21476868-21477267 | Common:2; Rare:128 | ||||
| chr14:21526279-21526489 | Rare:42 | ||||
| chr14:22589012-22589381 | Common:4; Rare:113 | ||||
| chr14:22766551-22766762 | Common:1; Rare:124 | ||||
| chr14:22829778-22829919 | Rare:52 | ||||
| chr14:22872102-22872188 | Common:2; Rare:16 |