Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77926385-77926888 | Common:2; Rare:141; Clinvar:16; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr1:77947806-77948003 | Rare:38 | ||||
chr1:77948239-77948268 | Rare:6 | ||||
chr1:77978901-77979334 | Common:4; Rare:153 | ||||
chr1:77979499-77979536 | Rare:12 | ||||
chr1:78004552-78004971 | Common:4; Rare:94 | ||||
chr1:79006674-79006876 | Common:1; Rare:71 | ||||
chr1:84690378-84690613 | Rare:83 | ||||
chr1:85062183-85062369 | Common:2; Rare:43 | ||||
chr1:85276314-85276680 | Common:6; Rare:126; Clinvar (benign):3 | ||||
chr1:85464578-85464897 | Common:5; Rare:100 | ||||
chr1:85577997-85578365 | Common:3; Rare:56 | ||||
chr1:85580664-85580772 | Rare:23 | ||||
chr1:85707836-85708015 | Common:1; Rare:51 | ||||
chr1:85708029-85708272 | Common:2; Rare:66 |