Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4847246-4847439 | Common:1; Rare:83 | ||||
chr16:8797607-8797910 | Common:1; Rare:123; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
chr16:11976624-11976755 | Common:2; Rare:46 | ||||
chr16:20806437-20806610 | Rare:58 | ||||
chr16:21599364-21599651 | Common:4; Rare:102 | ||||
chr16:23641295-23641539 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
chr16:25111478-25111762 | Common:2; Rare:66 | ||||
chr16:27549895-27550167 | Common:2; Rare:99 | ||||
chr16:28823957-28824090 | Rare:34 | ||||
chr16:28846261-28846643 | Common:2; Rare:129; Clinvar:6; Clinvar (benign):6 | ||||
chr16:29805519-29805760 | Common:2; Rare:110 | ||||
chr16:29807948-29808165 | Rare:124 | ||||
chr16:29995610-29995701 | Rare:42 | ||||
chr16:29996070-29996271 | Common:2; Rare:71 | ||||
chr16:30407484-30407656 | Rare:59 |