Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:75791273-75791387 | Rare:23 | ||||
chr1:77219368-77219520 | Rare:74 | ||||
chr1:77721889-77722072 | Rare:44 | ||||
chr1:77926362-77926462 | Common:1; Rare:29; Clinvar (benign):2 | ||||
chr1:77926532-77926890 | Common:1; Rare:111; Clinvar:14; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr1:77946325-77946429 | Rare:17 | ||||
chr1:77947786-77948014 | Rare:45 | ||||
chr1:77978880-77979496 | Common:6; Rare:189 | ||||
chr1:77979499-77979559 | Rare:20 | ||||
chr1:78004551-78004986 | Common:4; Rare:96 | ||||
chr1:81699293-81699767 | Common:4; Rare:74 | ||||
chr1:84077901-84078270 | Common:1; Rare:116 | ||||
chr1:84479194-84479567 | Common:3; Rare:166 | ||||
chr1:84506493-84506731 | Common:3; Rare:41 | ||||
chr1:84574380-84574557 | Common:3; Rare:58 |