Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77888087-77888413 | Common:2; Rare:76 | ||||
chr1:77888442-77888722 | Common:1; Rare:65; Clinvar:2 | ||||
chr1:77926595-77926887 | Common:1; Rare:92; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr1:77960182-77960380 | Rare:47 | ||||
chr1:77978880-77979344 | Common:4; Rare:160 | ||||
chr1:77979470-77979616 | Common:1; Rare:44 | ||||
chr1:78004551-78004901 | Common:3; Rare:85 | ||||
chr1:81306254-81306348 | Rare:17 | ||||
chr1:84077854-84078269 | Common:3; Rare:138 | ||||
chr1:84298414-84298500 | Common:1; Rare:26 | ||||
chr1:84479185-84479410 | Common:3; Rare:106 | ||||
chr1:84574385-84574587 | Common:2; Rare:62 | ||||
chr1:84690337-84690843 | Rare:179 | ||||
chr1:84893109-84893308 | Common:2; Rare:57 | ||||
chr1:84997107-84997234 | Common:6; Rare:37 |