Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:98446835-98446971 | Rare:35; Clinvar:1 | ||||
chr10:99430602-99430998 | Common:3; Rare:96 | ||||
chr10:99659239-99659556 | Common:1; Rare:80 | ||||
chr10:99732070-99732360 | Rare:109; Clinvar:5; Clinvar (benign):1 | ||||
chr10:99913971-99914142 | Rare:55 | ||||
chr10:100185895-100186198 | Rare:113 | ||||
chr10:100229553-100229689 | Rare:49 | ||||
chr10:100267606-100267768 | Common:3; Rare:48 | ||||
chr10:100286343-100286431 | Rare:20 | ||||
chr10:100286605-100286763 | Common:5; Rare:88 | ||||
chr10:100346921-100347438 | Common:3; Rare:118 | ||||
chr10:100529831-100530006 | Common:1; Rare:48 | ||||
chr10:100912751-100913031 | Common:1; Rare:86 | ||||
chr10:100913327-100913464 | Rare:35 | ||||
chr10:100987205-100987602 | Common:1; Rare:145; Clinvar:1; Clinvar (benign):1 |