Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:61762235-61762380 | Rare:34 | ||||
chr14:64503628-64503887 | Common:2; Rare:100 | ||||
chr14:66508409-66508518 | Rare:42 | ||||
chr14:67359768-67359999 | Rare:74 | ||||
chr14:67600257-67600333 | Common:1; Rare:21 | ||||
chr14:67816572-67816769 | Rare:36 | ||||
chr14:68793034-68793173 | Rare:39 | ||||
chr14:69398263-69398381 | Rare:45 | ||||
chr14:69611469-69611708 | Common:1; Rare:81 | ||||
chr14:73886768-73886869 | Common:1; Rare:31 | ||||
chr14:73950054-73950322 | Common:6; Rare:112; Clinvar (benign):4 | ||||
chr14:74019265-74019411 | Common:1; Rare:58 | ||||
chr14:74493290-74493789 | Common:4; Rare:159; Clinvar:2; Clinvar (benign):4 | ||||
chr14:74713082-74713200 | Rare:60 | ||||
chr14:75002754-75002943 | Common:1; Rare:50; Clinvar:2 |