Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161159392-161159532 | Common:1; Rare:40 | ||||
chr1:161166257-161166511 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161197291-161197423 | Common:2; Rare:18 | ||||
chr1:161198972-161199326 | Rare:55 | ||||
chr1:161201726-161202046 | Common:1; Rare:66 | ||||
chr1:161225731-161226063 | Common:10; Rare:49 | ||||
chr1:161314254-161314412 | Common:3; Rare:60; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161367857-161367991 | Rare:31 | ||||
chr1:161524237-161524540 | Common:5; Rare:94 | ||||
chr1:161549792-161549896 | Rare:36 | ||||
chr1:161766162-161766372 | Common:3; Rare:63 | ||||
chr1:162497761-162497859 | Common:1; Rare:33 | ||||
chr1:162561336-162561696 | Common:3; Rare:137 | ||||
chr1:162790516-162790805 | Common:4; Rare:86 | ||||
chr1:163321723-163321957 | Common:1; Rare:62 |