Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:37608788-37609031 | Common:1; Rare:73 | ||||
chr22:37675327-37675710 | Common:4; Rare:104 | ||||
chr22:37849286-37849480 | Rare:118 | ||||
chr22:37953532-37953765 | Common:1; Rare:93 | ||||
chr22:38181799-38182064 | Common:2; Rare:68 | ||||
chr22:38656360-38656716 | Common:1; Rare:90 | ||||
chr22:38681810-38682239 | Common:3; Rare:164 | ||||
chr22:38872186-38872483 | Rare:80 | ||||
chr22:39319594-39319826 | Common:3; Rare:100 | ||||
chr22:39502141-39502400 | Rare:73 | ||||
chr22:40044560-40044862 | Common:2; Rare:68 | ||||
chr22:40346441-40346556 | Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
chr22:40819294-40819506 | Common:11; Rare:105 | ||||
chr22:40856364-40856737 | Common:1; Rare:168 | ||||
chr22:40856939-40857159 | Common:1; Rare:93; Clinvar:3 |