Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:89701448-89701643 | Common:1; Rare:50 | ||||
chr10:92574034-92574149 | Common:1; Rare:35 | ||||
chr10:93482275-93482334 | Rare:9 | ||||
chr10:93702510-93702681 | Common:3; Rare:57 | ||||
chr10:94545653-94545856 | Common:3; Rare:65 | ||||
chr10:95693917-95694236 | Common:5; Rare:89; Clinvar (benign):1 | ||||
chr10:95907865-95907928 | Common:1; Rare:19 | ||||
chr10:97445975-97446229 | Rare:67 | ||||
chr10:98268182-98268458 | Common:3; Rare:70 | ||||
chr10:99732072-99732284 | Rare:70; Clinvar:4 | ||||
chr10:100529836-100529983 | Rare:40 | ||||
chr10:100987256-100987562 | Common:1; Rare:113; Clinvar (benign):1 | ||||
chr10:100996969-100997102 | Common:1; Rare:38 | ||||
chr10:101588173-101588329 | Rare:67 | ||||
chr10:102714282-102714631 | Common:2; Rare:117 |