Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43358674-43359102 | Common:7; Rare:129 | ||||
chr1:43367975-43368212 | Rare:65 | ||||
chr1:43389752-43389905 | Common:2; Rare:65 | ||||
chr1:44775462-44775599 | Rare:53 | ||||
chr1:44775815-44776080 | Common:2; Rare:101 | ||||
chr1:45012041-45012268 | Common:1; Rare:81; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45340028-45340212 | Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
chr1:45521871-45522087 | Common:1; Rare:83 | ||||
chr1:45686515-45686741 | Rare:80 | ||||
chr1:45687059-45687353 | Common:1; Rare:77 | ||||
chr1:45688061-45688211 | Common:1; Rare:39 | ||||
chr1:46303275-46303747 | Common:2; Rare:137 | ||||
chr1:47314093-47314451 | Common:3; Rare:76; Clinvar:1 | ||||
chr1:47333780-47333941 | Common:1; Rare:60 | ||||
chr1:50969992-50970268 | Rare:49 |