Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:55215071-55215423 | Rare:116 | ||||
chr1:55215448-55215559 | Rare:29 | ||||
chr1:58577220-58577557 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr1:58577665-58577915 | Common:3; Rare:29 | ||||
chr1:58699990-58700288 | Common:4; Rare:123 | ||||
chr1:58783901-58784099 | Rare:53 | ||||
chr1:58784304-58784425 | Common:2; Rare:28 | ||||
chr1:59296508-59296833 | Common:12; Rare:84 | ||||
chr1:59297003-59297117 | Common:3; Rare:45 | ||||
chr1:59673674-59673700 | Rare:8 | ||||
chr1:59673957-59674115 | Rare:59 | ||||
chr1:59814726-59815048 | Common:2; Rare:101 | ||||
chr1:61082508-61082775 | Common:2; Rare:88 | ||||
chr1:61724956-61725231 | Common:1; Rare:120 | ||||
chr1:61742311-61742551 | Rare:66 |