Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89065194-89065413 | Rare:30 | ||||
chr1:89198851-89199001 | Rare:22 | ||||
chr1:89820906-89821219 | Common:1; Rare:99 | ||||
chr1:89994973-89995193 | Common:2; Rare:81 | ||||
chr1:91021963-91022192 | Rare:68 | ||||
chr1:91022194-91022319 | Rare:26 | ||||
chr1:92298945-92299075 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92831972-92832113 | Common:1; Rare:79; Clinvar:6; Clinvar (benign):5 | ||||
chr1:92961430-92961585 | Rare:60 | ||||
chr1:93179602-93179970 | Common:2; Rare:68 | ||||
chr1:93180031-93180738 | Common:1; Rare:272 | ||||
chr1:93345772-93345946 | Common:4; Rare:67 | ||||
chr1:93447996-93448252 | Common:2; Rare:84 | ||||
chr1:93879110-93879269 | Common:1; Rare:60 | ||||
chr1:94237573-94237728 | Rare:60 |