Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:94410782-94410942 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
chr7:94412003-94412233 | Rare:60; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr7:94415162-94415312 | Rare:39; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr7:94418426-94418806 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr7:94420218-94420357 | Rare:40; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr7:95396931-95397168 | Common:3; Rare:37 | ||||
chr7:100335856-100336151 | Common:1; Rare:98 | ||||
chr7:100681862-100682164 | Rare:107 | ||||
chr7:102822433-102822640 | Common:3; Rare:27 | ||||
chr7:103280234-103280555 | Common:3; Rare:86 | ||||
chr7:103323605-103323766 | Rare:37 | ||||
chr7:105013028-105013207 | Common:1; Rare:63 | ||||
chr7:107924369-107924541 | Common:1; Rare:30 | ||||
chr7:107935643-107935676 | Rare:8 | ||||
chr7:108047301-108047337 | Rare:7 |