Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77888430-77888694 | Common:1; Rare:58; Clinvar:2 | ||||
chr1:77941819-77942114 | Common:1; Rare:84; Clinvar:4; Clinvar (benign):2 | ||||
chr1:77978985-77979224 | Common:2; Rare:93 | ||||
chr1:78004551-78004883 | Common:3; Rare:82 | ||||
chr1:78045792-78046313 | Common:1; Rare:179 | ||||
chr1:78490731-78491048 | Common:3; Rare:62; Clinvar:1 | ||||
chr1:84077904-84078130 | Common:1; Rare:83 | ||||
chr1:84297727-84298039 | Common:2; Rare:48 | ||||
chr1:84298439-84298546 | Rare:32 | ||||
chr1:84299203-84299299 | Rare:17 | ||||
chr1:84299314-84299609 | Common:1; Rare:60 | ||||
chr1:84690425-84690706 | Rare:91 | ||||
chr1:84997063-84997225 | Common:7; Rare:47 | ||||
chr1:85276019-85276307 | Common:5; Rare:70 | ||||
chr1:85276336-85276769 | Common:6; Rare:137; Clinvar (benign):2 |