Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:75710598-75710774 | Common:2; Rare:66 | ||||
chr2:75710872-75710979 | Common:1; Rare:40 | ||||
chr2:84459161-84459598 | Common:3; Rare:119; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr2:84516338-84516522 | Rare:50 | ||||
chr2:84905517-84905718 | Common:1; Rare:64 | ||||
chr2:84905756-84906116 | Common:1; Rare:93 | ||||
chr2:85327916-85328095 | Common:3; Rare:80 | ||||
chr2:85354479-85354807 | Common:1; Rare:114 | ||||
chr2:85413557-85413827 | Rare:57 | ||||
chr2:85413965-85414097 | Common:1; Rare:27 | ||||
chr2:85433631-85433961 | Rare:61 | ||||
chr2:85538755-85538842 | Common:2; Rare:25 | ||||
chr2:85539064-85539363 | Common:3; Rare:148; Clinvar (benign):7 | ||||
chr2:85561424-85561611 | Rare:64; Clinvar:4 | ||||
chr2:85577470-85577648 | Common:1; Rare:52 |