Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93680202-93680308 | Common:1; Rare:20 | ||||
chr1:93902021-93902125 | Rare:13 | ||||
chr1:93904516-93904683 | Common:1; Rare:23 | ||||
chr1:93908234-93908266 | Rare:4 | ||||
chr1:93920836-93921028 | Common:3; Rare:30 | ||||
chr1:94045564-94045599 | Rare:7 | ||||
chr1:94048442-94048767 | Common:2; Rare:65 | ||||
chr1:94048897-94049061 | Common:2; Rare:38; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:94067297-94067540 | Common:5; Rare:52 | ||||
chr1:94068246-94068541 | Common:1; Rare:55 | ||||
chr1:94069012-94069224 | Rare:28 | ||||
chr1:94069728-94069758 | Rare:5 | ||||
chr1:94069806-94070304 | Common:2; Rare:86 | ||||
chr1:94092275-94092566 | Common:2; Rare:49 | ||||
chr1:94094038-94094316 | Common:4; Rare:49 |