| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101762051-101762131 | Common:2; Rare:16 | ||||
| chr14:101762443-101762474 | Rare:7 | ||||
| chr14:101809686-101809971 | Rare:62 | ||||
| chr14:101810178-101810475 | Common:2; Rare:55 | ||||
| chr14:101964390-101964677 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:101964717-101964957 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr14:102086344-102086408 | Rare:38 | ||||
| chr14:102086414-102086646 | Common:3; Rare:115 | ||||
| chr14:102086781-102086871 | Common:2; Rare:36 | ||||
| chr14:102086907-102087266 | Common:6; Rare:144 | ||||
| chr14:102087276-102087812 | Common:5; Rare:192 | ||||
| chr14:102139215-102139471 | Rare:107 | ||||
| chr14:102139606-102140041 | Rare:147 | ||||
| chr14:102140430-102140755 | Common:1; Rare:88 | ||||
| chr14:102234489-102234551 | Rare:12 |