Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:218345977-218346092 | Common:5; Rare:39; Clinvar:7; Clinvar (benign):3 | ||||
chr1:218346145-218346361 | Rare:33 | ||||
chr1:218346775-218346959 | Rare:41; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:218347362-218347520 | Common:2; Rare:26 | ||||
chr1:219173771-219173911 | Common:1; Rare:76 | ||||
chr1:220093894-220094246 | Common:12; Rare:116; Clinvar (benign):2 | ||||
chr1:220272323-220272572 | Rare:73; Clinvar:5 | ||||
chr1:222589862-222589984 | Common:2; Rare:32 | ||||
chr1:222617879-222618117 | Common:3; Rare:61 | ||||
chr1:222644146-222644387 | Common:1; Rare:71 | ||||
chr1:222712424-222712864 | Common:3; Rare:151 | ||||
chr1:222713203-222713466 | Common:1; Rare:81 | ||||
chr1:223143236-223143338 | Common:2; Rare:25 | ||||
chr1:224113982-224114141 | Common:1; Rare:57 | ||||
chr1:224183111-224183312 | Common:2; Rare:94 |