Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:50960116-50960271 | Rare:53 | ||||
chr1:50969922-50970300 | Common:1; Rare:78 | ||||
chr1:51236193-51236401 | Common:2; Rare:80 | ||||
chr1:51789394-51789678 | Rare:88 | ||||
chr1:51795921-51796089 | Common:1; Rare:33 | ||||
chr1:51878267-51878472 | Common:1; Rare:65 | ||||
chr1:52055070-52055271 | Common:1; Rare:60 | ||||
chr1:52056119-52056335 | Common:1; Rare:63 | ||||
chr1:52404436-52404633 | Common:1; Rare:61 | ||||
chr1:52552938-52553386 | Common:4; Rare:134 | ||||
chr1:53196673-53196872 | Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
chr1:53238379-53238598 | Rare:70 | ||||
chr1:53328110-53328253 | Rare:38 | ||||
chr1:53945561-53946077 | Common:8; Rare:138 | ||||
chr1:53946252-53946686 | Common:3; Rare:137 |