Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:36387818-36388043 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
chr22:36388339-36388601 | Common:6; Rare:63 | ||||
chr22:37019445-37019797 | Common:5; Rare:97 | ||||
chr22:37560371-37560516 | Rare:48 | ||||
chr22:37675365-37675680 | Common:3; Rare:92 | ||||
chr22:37849307-37849474 | Rare:96 | ||||
chr22:37953577-37953756 | Rare:77 | ||||
chr22:38656391-38656741 | Common:1; Rare:80 | ||||
chr22:38681780-38682239 | Common:3; Rare:172 | ||||
chr22:38700931-38701098 | Rare:62 | ||||
chr22:38755418-38755559 | Common:1; Rare:30 | ||||
chr22:39319607-39319797 | Common:2; Rare:83 | ||||
chr22:39399656-39399818 | Common:3; Rare:67 | ||||
chr22:40346441-40346578 | Rare:61; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr22:40856437-40856730 | Rare:131 |