Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1020589-1020657 | Rare:17 | ||||
chr1:1033601-1033903 | Common:1; Rare:47 | ||||
chr1:1115897-1116191 | Rare:84 | ||||
chr1:1231469-1231664 | Common:1; Rare:56 | ||||
chr1:1231820-1232338 | Rare:178; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:1232428-1232564 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
chr1:1273137-1273294 | Rare:50 | ||||
chr1:1273774-1274169 | Common:4; Rare:142 | ||||
chr1:1274226-1274266 | Common:1; Rare:8 | ||||
chr1:1304754-1304936 | Common:2; Rare:50 | ||||
chr1:1305632-1305818 | Common:1; Rare:62 | ||||
chr1:1306180-1306200 | Common:1; Rare:6 | ||||
chr1:1307827-1308189 | Rare:90 | ||||
chr1:1308307-1308652 | Common:8; Rare:142 | ||||
chr1:1308662-1308826 | Common:2; Rare:66 |