Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:3443481-3443732 | Common:3; Rare:86 | ||||
chr16:3717510-3717639 | Rare:64 | ||||
chr16:4538394-4538561 | Common:2; Rare:47 | ||||
chr16:4847268-4847436 | Common:1; Rare:72 | ||||
chr16:4890332-4890591 | Common:4; Rare:85 | ||||
chr16:8797618-8797879 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
chr16:11345251-11345461 | Common:1; Rare:73 | ||||
chr16:11797187-11797527 | Common:3; Rare:132 | ||||
chr16:11976629-11976758 | Rare:45 | ||||
chr16:14975003-14975167 | Common:2; Rare:41 | ||||
chr16:20806435-20806655 | Rare:71 | ||||
chr16:20900352-20900679 | Common:3; Rare:70 | ||||
chr16:21303030-21303320 | Rare:58 | ||||
chr16:21599364-21599657 | Common:4; Rare:104 | ||||
chr16:21953005-21953409 | Common:1; Rare:102; Clinvar (benign):3 |