Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:72051921-72052119 | Rare:41 | ||||
chr16:72073769-72073972 | Common:2; Rare:86 | ||||
chr16:72664947-72665145 | Common:1; Rare:58 | ||||
chr16:74368127-74368367 | Common:1; Rare:69 | ||||
chr16:76532276-76532524 | Common:1; Rare:51 | ||||
chr16:79598316-79598796 | Common:12; Rare:120 | ||||
chr16:85536913-85537081 | Common:1; Rare:42 | ||||
chr16:87839145-87839493 | Common:5; Rare:82 | ||||
chr16:87839718-87839976 | Common:3; Rare:64 | ||||
chr16:87841653-87841697 | Common:1; Rare:13 | ||||
chr16:87841699-87842079 | Common:1; Rare:85 | ||||
chr16:87856285-87856457 | Common:1; Rare:45 | ||||
chr17:1712589-1712836 | Common:2; Rare:56 | ||||
chr17:1725460-1725688 | Rare:72 | ||||
chr17:1744904-1745213 | Common:2; Rare:90; Clinvar (benign):2 |