| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101823501-101823885 | Rare:91 | ||||
| chr14:101964420-101964721 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:101964723-101964824 | Common:1; Rare:25; Clinvar:2; Clinvar (benign):4 | ||||
| chr14:102039520-102039731 | Common:1; Rare:60; Clinvar (benign):4 | ||||
| chr14:102084398-102085062 | Common:1; Rare:301 | ||||
| chr14:102086978-102087429 | Common:5; Rare:195 | ||||
| chr14:102087586-102087598 | Rare:2 | ||||
| chr14:102139667-102139935 | Rare:94 | ||||
| chr14:102305048-102305333 | Common:1; Rare:86 | ||||
| chr14:102362849-102363107 | Rare:114 | ||||
| chr14:102592424-102592663 | Common:1; Rare:97 | ||||
| chr14:102922558-102922691 | Common:4; Rare:51 | ||||
| chr14:102928469-102928687 | Rare:76 | ||||
| chr14:103333969-103334260 | Common:1; Rare:122 | ||||
| chr14:103385755-103385863 | Common:1; Rare:29 |