| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50532494-50532823 | Common:4; Rare:100 | ||||
| chr14:50944401-50944538 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51554501-51554696 | Rare:38 | ||||
| chr14:51651554-51651993 | Common:4; Rare:120 | ||||
| chr14:51989388-51989626 | Common:2; Rare:75 | ||||
| chr14:52707033-52707240 | Common:1; Rare:91 | ||||
| chr14:52791427-52791785 | Common:2; Rare:117 | ||||
| chr14:55027049-55027290 | Common:2; Rare:69 | ||||
| chr14:55051462-55051743 | Rare:121 | ||||
| chr14:55191538-55191746 | Common:5; Rare:47 | ||||
| chr14:55411823-55411944 | Common:2; Rare:58 | ||||
| chr14:55580102-55580285 | Common:2; Rare:81 | ||||
| chr14:57268819-57269090 | Common:2; Rare:84 | ||||
| chr14:57493731-57494023 | Common:1; Rare:59 | ||||
| chr14:58199855-58200207 | Common:4; Rare:133 |