Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100296336-100296475 | Common:1; Rare:25 | ||||
chr14:100376264-100376502 | Common:3; Rare:79 | ||||
chr14:101809694-101810030 | Rare:81 | ||||
chr14:101964395-101964824 | Common:4; Rare:129; Clinvar:4; Clinvar (benign):7 | ||||
chr14:102027621-102028141 | Rare:101; Clinvar:8; Clinvar (benign):9 | ||||
chr14:102039433-102039732 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):7 | ||||
chr14:102086978-102087330 | Common:4; Rare:143 | ||||
chr14:102139655-102139957 | Rare:104 | ||||
chr14:102305124-102305308 | Common:1; Rare:60 | ||||
chr14:102362847-102363094 | Rare:112 | ||||
chr14:102928497-102928692 | Rare:69 | ||||
chr14:103333977-103334257 | Rare:117 | ||||
chr14:103521080-103521243 | Common:1; Rare:60 | ||||
chr14:103529029-103529255 | Common:1; Rare:70 | ||||
chr14:103562223-103562375 | Rare:62 |