Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2673351-2673684 | Common:10; Rare:114 | ||||
chr16:3686093-3686275 | Common:2; Rare:55 | ||||
chr16:4887141-4887380 | Common:2; Rare:80 | ||||
chr16:4902992-4903151 | Common:1; Rare:40 | ||||
chr16:5020550-5020802 | Common:2; Rare:68 | ||||
chr16:8843423-8843612 | Common:5; Rare:67 | ||||
chr16:8847485-8847829 | Rare:142; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):8 | ||||
chr16:21519991-21520253 | Common:4; Rare:112 | ||||
chr16:21520379-21520732 | Common:1; Rare:45 | ||||
chr16:21820380-21820560 | Rare:55 | ||||
chr16:25066824-25066907 | Common:3; Rare:31 | ||||
chr16:27718763-27719084 | Common:1; Rare:55 | ||||
chr16:29139634-29139696 | Rare:13 | ||||
chr16:30334782-30334952 | Common:1; Rare:50 | ||||
chr16:30335333-30335438 | Common:1; Rare:35 |