Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149812148-149812523 | Common:2; Rare:170 | ||||
chr1:149842746-149842962 | Rare:3 | ||||
chr1:149850889-149851063 | |||||
chr1:149886605-149887184 | Common:3; Rare:226 | ||||
chr1:149887859-149888186 | Rare:106 | ||||
chr1:150067606-150067873 | Common:1; Rare:75 | ||||
chr1:150282299-150282596 | Common:3; Rare:59 | ||||
chr1:150321413-150321602 | Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363919-150364225 | Common:4; Rare:106 | ||||
chr1:150552485-150552591 | Rare:30 | ||||
chr1:150558084-150558369 | Rare:66; Clinvar (pathogenic):1 | ||||
chr1:150578705-150578861 | Common:3; Rare:44 | ||||
chr1:150579151-150579311 | Rare:66 | ||||
chr1:150579595-150579830 | Common:9; Rare:75 | ||||
chr1:150629112-150629392 | Common:1; Rare:85 |