Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74507669-74507789 | Rare:25 | ||||
chr2:74529668-74530009 | Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74554411-74554757 | Common:2; Rare:102 | ||||
chr2:74958431-74958742 | Common:6; Rare:112 | ||||
chr2:74958876-74959071 | Rare:70 | ||||
chr2:75199509-75199588 | Rare:10 | ||||
chr2:75710872-75711250 | Common:2; Rare:97 | ||||
chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:84905504-84905953 | Common:2; Rare:136 | ||||
chr2:85327915-85328092 | Common:3; Rare:79 | ||||
chr2:85354496-85354786 | Common:1; Rare:97 | ||||
chr2:85376772-85376914 | Rare:18 | ||||
chr2:85538989-85539207 | Common:3; Rare:94 | ||||
chr2:85561432-85561574 | Rare:52; Clinvar:4 | ||||
chr2:85584294-85584472 | Common:2; Rare:51 |