Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:31753745-31753982 | Rare:80 | ||||
chr22:31944414-31944702 | Common:2; Rare:116 | ||||
chr22:32412201-32412298 | Common:1; Rare:30 | ||||
chr22:35299713-35299957 | Common:2; Rare:64 | ||||
chr22:35380805-35381108 | Common:11; Rare:114 | ||||
chr22:35399904-35400195 | Rare:102 | ||||
chr22:36387975-36388322 | Common:2; Rare:98; Clinvar (benign):1 | ||||
chr22:36529095-36529521 | Common:6; Rare:131 | ||||
chr22:37849324-37849476 | Rare:85 | ||||
chr22:37953644-37953771 | Rare:56 | ||||
chr22:38181818-38182072 | Common:2; Rare:69 | ||||
chr22:38570184-38570483 | Common:5; Rare:53 | ||||
chr22:38656391-38656687 | Common:1; Rare:65 | ||||
chr22:38681858-38682026 | Common:1; Rare:77 | ||||
chr22:39399629-39399805 | Common:3; Rare:69 |