Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212858076-212858303 | Common:4; Rare:59; Clinvar:2 | ||||
chr1:213015443-213015647 | Rare:61 | ||||
chr1:213051192-213051370 | Rare:64 | ||||
chr1:214280923-214281257 | Common:4; Rare:138 | ||||
chr1:214551553-214551939 | Common:2; Rare:123 | ||||
chr1:215567141-215567417 | Common:1; Rare:75 | ||||
chr1:217631009-217631385 | Common:3; Rare:110 | ||||
chr1:219173786-219173900 | Common:1; Rare:64 | ||||
chr1:220094268-220094411 | Common:1; Rare:43; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:220272307-220272588 | Rare:80; Clinvar:5 | ||||
chr1:220786734-220787213 | Common:5; Rare:120 | ||||
chr1:220879199-220879519 | Common:9; Rare:84 | ||||
chr1:220879603-220879743 | Rare:33 | ||||
chr1:220881397-220881534 | Common:1; Rare:33 | ||||
chr1:221742041-221742288 | Rare:65 |