Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100912678-100913029 | Common:1; Rare:103 | ||||
chr10:100987243-100987571 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996990-100997138 | Rare:42 | ||||
chr10:101031113-101031302 | Common:1; Rare:40 | ||||
chr10:101588144-101588333 | Rare:76 | ||||
chr10:101818323-101818762 | Common:1; Rare:121 | ||||
chr10:102114958-102115133 | Common:2; Rare:50 | ||||
chr10:102132879-102133066 | Rare:43 | ||||
chr10:102394337-102394570 | Rare:64 | ||||
chr10:102395579-102395729 | Common:1; Rare:43 | ||||
chr10:102432546-102432783 | Common:1; Rare:68 | ||||
chr10:102714275-102714636 | Common:2; Rare:121 | ||||
chr10:102776041-102776269 | Common:1; Rare:35 | ||||
chr10:103193243-103193338 | Common:5; Rare:35; Clinvar (benign):1 | ||||
chr10:103396411-103396709 | Rare:106 |