| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50397033-50397303 | Rare:119 | ||||
| chr14:50531725-50532134 | Common:1; Rare:115 | ||||
| chr14:50532154-50532268 | Common:1; Rare:23 | ||||
| chr14:50532315-50532394 | Rare:11 | ||||
| chr14:50532415-50532731 | Common:3; Rare:96 | ||||
| chr14:50560078-50560309 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:50560381-50560685 | Common:1; Rare:72 | ||||
| chr14:50560710-50560896 | Common:4; Rare:37 | ||||
| chr14:50560976-50561139 | Rare:27 | ||||
| chr14:50561180-50561312 | Common:1; Rare:20 | ||||
| chr14:50667660-50667952 | Rare:98 | ||||
| chr14:50668187-50668466 | Common:3; Rare:94 | ||||
| chr14:50668489-50668662 | Common:11; Rare:93 | ||||
| chr14:50668788-50669054 | Common:2; Rare:57 | ||||
| chr14:50830503-50830813 | Common:2; Rare:80 |