Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70354634-70354919 | Rare:90 | ||||
chr1:70354998-70355061 | Rare:31 | ||||
chr1:70410749-70410880 | Rare:25 | ||||
chr1:70410994-70411357 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080968-71081435 | Rare:133 | ||||
chr1:74198035-74198473 | Common:4; Rare:196 | ||||
chr1:74673815-74674017 | Common:2; Rare:41 | ||||
chr1:74732966-74733443 | Common:6; Rare:167 | ||||
chr1:74733803-74733903 | Rare:16 | ||||
chr1:75724221-75724472 | Common:4; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
chr1:75724495-75725039 | Common:6; Rare:187; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:75785914-75786379 | Common:5; Rare:156 | ||||
chr1:76074539-76074752 | Common:2; Rare:85 | ||||
chr1:77219291-77219572 | Common:1; Rare:122 | ||||
chr1:77682547-77682724 | Rare:42 |