Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97445975-97446225 | Rare:66 | ||||
chr10:97469702-97469767 | Common:1; Rare:22 | ||||
chr10:97498358-97498533 | Common:1; Rare:81 | ||||
chr10:97498694-97499099 | Common:2; Rare:119 | ||||
chr10:97633436-97633618 | Common:2; Rare:45 | ||||
chr10:97687184-97687460 | Common:6; Rare:83 | ||||
chr10:98446822-98447048 | Rare:68; Clinvar:1 | ||||
chr10:99430616-99430994 | Common:3; Rare:90 | ||||
chr10:99532728-99532995 | Common:4; Rare:59 | ||||
chr10:99659219-99659571 | Common:2; Rare:91 | ||||
chr10:99732056-99732344 | Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185884-100186198 | Rare:115 | ||||
chr10:100229560-100229640 | Rare:23 | ||||
chr10:100267606-100267735 | Common:3; Rare:41 | ||||
chr10:100286605-100286730 | Common:4; Rare:73 |