Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54887114-54887483 | Common:3; Rare:119; Clinvar:4; Clinvar (benign):1 | ||||
chr1:55215263-55215456 | Rare:80 | ||||
chr1:55215469-55215763 | Common:2; Rare:91 | ||||
chr1:56517003-56517131 | Common:1; Rare:19 | ||||
chr1:56579392-56579420 | Rare:8 | ||||
chr1:58546191-58546431 | Common:4; Rare:56 | ||||
chr1:58546604-58546969 | Common:4; Rare:114 | ||||
chr1:58699966-58700254 | Common:4; Rare:127 | ||||
chr1:58783881-58784431 | Common:2; Rare:144 | ||||
chr1:58784565-58784825 | Common:3; Rare:69 | ||||
chr1:59296275-59296414 | Rare:21 | ||||
chr1:59296440-59296648 | Common:3; Rare:48 | ||||
chr1:59296770-59297275 | Common:4; Rare:145 | ||||
chr1:59814419-59814993 | Common:4; Rare:165 | ||||
chr1:59926220-59926525 | Common:1; Rare:55 |