Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53946490-53946599 | Common:1; Rare:32 | ||||
chr1:54052507-54052882 | Common:1; Rare:76 | ||||
chr1:54053148-54053749 | Common:6; Rare:192 | ||||
chr1:54053933-54054073 | Common:1; Rare:25 | ||||
chr1:54054589-54054807 | Rare:42 | ||||
chr1:54199902-54200287 | Rare:110 | ||||
chr1:54200644-54200791 | Common:1; Rare:27 | ||||
chr1:54406322-54406634 | Common:4; Rare:128 | ||||
chr1:54542039-54542435 | Common:5; Rare:111 | ||||
chr1:54542438-54542899 | Common:1; Rare:98 | ||||
chr1:54715694-54715941 | Common:4; Rare:82 | ||||
chr1:54716078-54716143 | Rare:20 | ||||
chr1:54764388-54764870 | Common:7; Rare:143; Clinvar (benign):1 | ||||
chr1:54800818-54800873 | Rare:19 | ||||
chr1:54800909-54800976 | Common:1; Rare:22 |