| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102139572-102139949 | Common:1; Rare:129 | ||||
| chr14:102140117-102140157 | Rare:9 | ||||
| chr14:102140466-102140743 | Common:1; Rare:73 | ||||
| chr14:102305073-102305371 | Common:1; Rare:86 | ||||
| chr14:102316900-102317118 | Common:4; Rare:99 | ||||
| chr14:102317323-102317691 | Common:2; Rare:53 | ||||
| chr14:102319593-102320000 | Common:4; Rare:113 | ||||
| chr14:102320280-102320388 | Rare:34 | ||||
| chr14:102362809-102363125 | Common:1; Rare:134 | ||||
| chr14:102363273-102363341 | Rare:18 | ||||
| chr14:102438125-102438286 | Common:2; Rare:89; Clinvar (benign):1 | ||||
| chr14:102508487-102508711 | Common:2; Rare:40 | ||||
| chr14:102509008-102509110 | Common:1; Rare:10 | ||||
| chr14:102509176-102509391 | Common:4; Rare:32 | ||||
| chr14:102509662-102510108 | Common:1; Rare:125 |