Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99430621-99430936 | Common:3; Rare:71 | ||||
chr10:99659244-99659562 | Common:1; Rare:80 | ||||
chr10:99732076-99732331 | Rare:93; Clinvar:3 | ||||
chr10:100185905-100186198 | Rare:112 | ||||
chr10:100229562-100229629 | Rare:18 | ||||
chr10:100267623-100267746 | Common:2; Rare:34 | ||||
chr10:100529844-100529968 | Rare:35 | ||||
chr10:100912751-100913038 | Common:1; Rare:89 | ||||
chr10:100987445-100987571 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031113-101031292 | Common:1; Rare:38 | ||||
chr10:101588205-101588329 | Rare:50 | ||||
chr10:101818355-101818762 | Common:1; Rare:108 | ||||
chr10:102394337-102394559 | Rare:63 | ||||
chr10:102395589-102395721 | Rare:36 | ||||
chr10:102432556-102432774 | Common:1; Rare:62 |