Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70411059-70411276 | Common:1; Rare:54; Clinvar:1 | ||||
chr1:71066682-71066875 | Rare:63 | ||||
chr1:71067633-71067863 | Common:1; Rare:57 | ||||
chr1:71067915-71068035 | Rare:21 | ||||
chr1:71069191-71069357 | Rare:48 | ||||
chr1:71080937-71081411 | Rare:130 | ||||
chr1:72282293-72282597 | Common:1; Rare:98 | ||||
chr1:72282636-72283367 | Common:10; Rare:214 | ||||
chr1:74198126-74198351 | Common:3; Rare:120 | ||||
chr1:74732973-74733353 | Common:6; Rare:132 | ||||
chr1:75724626-75724830 | Common:2; Rare:95; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:75749207-75749538 | Rare:83; Clinvar:5; Clinvar (pathogenic):5 | ||||
chr1:75786094-75786594 | Common:7; Rare:161 | ||||
chr1:75786777-75787079 | Common:2; Rare:65 | ||||
chr1:75790865-75790981 | Common:3; Rare:25 |