Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:75724271-75724796 | Common:6; Rare:183; Clinvar:7; Clinvar (benign):5 | ||||
chr1:75732708-75732920 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
chr1:76074634-76074867 | Rare:66 | ||||
chr1:77219360-77219536 | Rare:82 | ||||
chr1:77683327-77683544 | Common:1; Rare:73 | ||||
chr1:77888037-77888224 | Rare:56 | ||||
chr1:77888227-77888430 | Common:2; Rare:41 | ||||
chr1:77888457-77888758 | Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77979000-77979318 | Common:2; Rare:111 | ||||
chr1:77979452-77979537 | Common:1; Rare:23 | ||||
chr1:78004546-78004960 | Common:4; Rare:97 | ||||
chr1:78619871-78620058 | Common:1; Rare:25 | ||||
chr1:79006656-79006876 | Common:1; Rare:78 | ||||
chr1:81800355-81800634 | Rare:92 | ||||
chr1:81800651-81800719 | Rare:23 |