Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99430622-99430965 | Common:3; Rare:83 | ||||
chr10:99659271-99659562 | Common:1; Rare:71 | ||||
chr10:99732072-99732335 | Rare:97; Clinvar:4 | ||||
chr10:100185938-100186180 | Rare:94 | ||||
chr10:100229553-100229664 | Rare:38 | ||||
chr10:100346928-100347252 | Common:1; Rare:81 | ||||
chr10:100912841-100913023 | Common:1; Rare:51 | ||||
chr10:100913335-100913456 | Rare:31 | ||||
chr10:100969326-100969526 | Common:3; Rare:43 | ||||
chr10:100987429-100987573 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996983-100997132 | Common:1; Rare:42 | ||||
chr10:100999608-100999924 | Common:2; Rare:95 | ||||
chr10:101031113-101031487 | Common:1; Rare:83 | ||||
chr10:101031502-101031533 | Rare:7 | ||||
chr10:101588166-101588340 | Rare:72 |