Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:31496418-31496556 | Common:1; Rare:37 | ||||
chr22:31753802-31753982 | Rare:59 | ||||
chr22:32412188-32412285 | Common:1; Rare:35 | ||||
chr22:32474944-32475313 | Common:2; Rare:123; Clinvar (benign):1 | ||||
chr22:32801491-32801706 | Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr22:35399904-35400199 | Rare:102 | ||||
chr22:36481604-36481734 | Common:2; Rare:33 | ||||
chr22:36529090-36529439 | Common:2; Rare:104 | ||||
chr22:37019427-37019757 | Common:5; Rare:93 | ||||
chr22:37560331-37560521 | Common:1; Rare:66 | ||||
chr22:37675368-37675710 | Common:4; Rare:98 | ||||
chr22:37849316-37849465 | Rare:85 | ||||
chr22:37953571-37953749 | Rare:76 | ||||
chr22:38570175-38570470 | Common:4; Rare:53 | ||||
chr22:38656391-38656687 | Common:1; Rare:65 |