Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:96391809-96392169 | Common:2; Rare:106 | ||||
chr14:96502261-96502614 | Common:2; Rare:147 | ||||
chr14:99480728-99481128 | Common:2; Rare:140 | ||||
chr14:99580095-99580258 | Rare:40 | ||||
chr14:100141032-100141137 | Rare:20 | ||||
chr14:100238536-100238851 | Common:3; Rare:90 | ||||
chr14:100238884-100239226 | Common:1; Rare:127 | ||||
chr14:100239716-100239915 | Common:2; Rare:69 | ||||
chr14:100375408-100375675 | Common:1; Rare:38 | ||||
chr14:100376264-100376504 | Common:3; Rare:79 | ||||
chr14:101809736-101810044 | Rare:73 | ||||
chr14:101964368-101964670 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
chr14:102027777-102028139 | Rare:70; Clinvar:3; Clinvar (benign):5 | ||||
chr14:102086987-102087383 | Common:5; Rare:169 | ||||
chr14:102139667-102139932 | Rare:93 |