Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86914302-86914632 | Common:2; Rare:81 | ||||
chr1:88684070-88684379 | Common:3; Rare:82 | ||||
chr1:89994981-89995165 | Common:2; Rare:74 | ||||
chr1:91021963-91022206 | Rare:73 | ||||
chr1:92298945-92299089 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92784640-92784953 | Common:1; Rare:77 | ||||
chr1:92785087-92785426 | Common:6; Rare:105 | ||||
chr1:92831884-92832117 | Common:1; Rare:107; Clinvar:7; Clinvar (benign):5 | ||||
chr1:93079114-93079280 | Common:2; Rare:73 | ||||
chr1:93180238-93180292 | Rare:22 | ||||
chr1:93180298-93180744 | Common:2; Rare:178 | ||||
chr1:93345788-93345912 | Common:3; Rare:50 | ||||
chr1:94541730-94541969 | Rare:75 | ||||
chr1:94926839-94926927 | Rare:23 | ||||
chr1:95233973-95234227 | Common:5; Rare:77 |