Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73167948-73168142 | Rare:50 | ||||
chr10:73252542-73252791 | Common:2; Rare:71; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73495618-73495757 | Rare:26 | ||||
chr10:73625850-73626113 | Rare:57 | ||||
chr10:73744243-73744435 | Common:1; Rare:53 | ||||
chr10:73781982-73782357 | Common:1; Rare:118 | ||||
chr10:73874465-73874820 | Rare:89 | ||||
chr10:73997756-73998205 | Common:2; Rare:120; Clinvar (benign):1 | ||||
chr10:74151053-74151275 | Common:1; Rare:68 | ||||
chr10:74176411-74176558 | Rare:35 | ||||
chr10:74176628-74176806 | Rare:49; Clinvar:3 | ||||
chr10:74825322-74825610 | Rare:76 | ||||
chr10:75210473-75210892 | Common:2; Rare:140 | ||||
chr10:78029446-78029643 | Common:1; Rare:62; Clinvar (benign):1 | ||||
chr10:80078608-80078715 | Rare:42 |