Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153634358-153634452 | Common:1; Rare:33 | ||||
chr1:153670916-153671247 | Rare:112 | ||||
chr1:153727739-153728092 | Common:1; Rare:107 | ||||
chr1:153963479-153963727 | Common:2; Rare:66 | ||||
chr1:153967309-153967512 | Common:1; Rare:39 | ||||
chr1:153967624-153967908 | Common:1; Rare:52 | ||||
chr1:153985374-153985511 | Rare:21 | ||||
chr1:153986202-153986463 | Rare:69 | ||||
chr1:153990673-153990826 | Common:2; Rare:78 | ||||
chr1:154182986-154183290 | Rare:97 | ||||
chr1:154219917-154220220 | Common:5; Rare:82 | ||||
chr1:154220504-154221004 | Common:1; Rare:170 | ||||
chr1:154272455-154272682 | Common:4; Rare:52; Clinvar:1; Clinvar (benign):3 | ||||
chr1:154627881-154628039 | Common:3; Rare:82 | ||||
chr1:154936668-154936762 | Common:2; Rare:31 |