| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101809686-101810034 | Rare:83 | ||||
| chr14:101810287-101810473 | Common:2; Rare:38 | ||||
| chr14:101964361-101964670 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102027663-102028109 | Rare:84; Clinvar:7; Clinvar (benign):6 | ||||
| chr14:102039485-102039662 | Common:1; Rare:60; Clinvar (benign):3 | ||||
| chr14:102086556-102086793 | Rare:103 | ||||
| chr14:102086978-102087377 | Common:5; Rare:169 | ||||
| chr14:102087455-102087667 | Common:3; Rare:61 | ||||
| chr14:102139306-102139406 | Rare:50 | ||||
| chr14:102139644-102140029 | Rare:133 | ||||
| chr14:102178807-102178949 | Common:1; Rare:30 | ||||
| chr14:102234481-102234834 | Common:2; Rare:68 | ||||
| chr14:102235442-102235518 | Rare:13 | ||||
| chr14:102316924-102317114 | Common:4; Rare:92 | ||||
| chr14:102362843-102363098 | Rare:115 |