Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70354692-70354862 | Rare:62 | ||||
chr1:70411027-70411291 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080997-71081364 | Rare:96 | ||||
chr1:74198148-74198324 | Common:1; Rare:102 | ||||
chr1:74733008-74733254 | Common:5; Rare:78 | ||||
chr1:77219398-77219488 | Rare:41 | ||||
chr1:77683331-77683604 | Common:1; Rare:87 | ||||
chr1:77888193-77888703 | Common:3; Rare:112; Clinvar:2 | ||||
chr1:77979020-77979233 | Common:2; Rare:77 | ||||
chr1:77979468-77979536 | Common:1; Rare:19 | ||||
chr1:78004552-78004971 | Common:4; Rare:94 | ||||
chr1:83999104-83999245 | Common:1; Rare:40 | ||||
chr1:84077904-84078124 | Common:1; Rare:80 | ||||
chr1:84506544-84506711 | Common:3; Rare:32 | ||||
chr1:84574416-84574542 | Common:1; Rare:41 |