Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10347772-10347941 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
chr1:10392511-10392566 | Rare:6 | ||||
chr1:10496046-10496357 | Common:2; Rare:56 | ||||
chr1:10523334-10523531 | Common:1; Rare:34 | ||||
chr1:10618196-10618394 | Rare:71; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11087520-11087905 | Rare:112 | ||||
chr1:11908227-11908339 | Common:25; Rare:121 | ||||
chr1:12001820-12002056 | Common:3; Rare:60; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr1:12459971-12460262 | Common:2; Rare:59 | ||||
chr1:12618294-12618521 | Common:1; Rare:44 | ||||
chr1:14138187-14138516 | Common:2; Rare:49 | ||||
chr1:14517626-14517791 | Rare:30 | ||||
chr1:15119260-15119332 | Rare:14 | ||||
chr1:15603579-15603730 | Common:3; Rare:45 | ||||
chr1:15635453-15635480 | Rare:9 |