Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154405011-154405169 | Common:3; Rare:20 | ||||
chr1:154405492-154405630 | Rare:25 | ||||
chr1:154501560-154502165 | Common:2; Rare:189 | ||||
chr1:154502362-154502555 | Common:3; Rare:57 | ||||
chr1:154502873-154502979 | Rare:30 | ||||
chr1:154558908-154559097 | Common:1; Rare:68 | ||||
chr1:154584940-154585254 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:154627889-154628011 | Common:3; Rare:65 | ||||
chr1:154859843-154860018 | Common:1; Rare:27 | ||||
chr1:154936618-154936762 | Common:2; Rare:50 | ||||
chr1:154936842-154937038 | Rare:39 | ||||
chr1:154956068-154956235 | Common:1; Rare:46 | ||||
chr1:154961364-154961568 | Rare:64 | ||||
chr1:154961712-154962041 | Common:1; Rare:114 | ||||
chr1:154968529-154968834 | Rare:93 |