Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:71080974-71081364 | Rare:107 | ||||
chr1:74198141-74198302 | Common:1; Rare:92 | ||||
chr1:74732989-74733266 | Common:5; Rare:87 | ||||
chr1:75724658-75724773 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):1 | ||||
chr1:77219385-77219501 | Rare:53 | ||||
chr1:77888079-77888224 | Rare:43 | ||||
chr1:77888233-77888758 | Common:3; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77979034-77979327 | Common:3; Rare:92 | ||||
chr1:77979534-77979551 | Rare:6 | ||||
chr1:78004552-78004994 | Common:4; Rare:95 | ||||
chr1:78490912-78491155 | Common:1; Rare:55 | ||||
chr1:84077866-84078141 | Common:1; Rare:105 | ||||
chr1:84506557-84506726 | Common:3; Rare:31 | ||||
chr1:84574378-84574578 | Common:3; Rare:64 | ||||
chr1:84690418-84690688 | Rare:83 |