Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100825915-100826166 | Rare:52 | ||||
chr14:100828335-100828771 | Common:3; Rare:56 | ||||
chr14:100830400-100830535 | Rare:20 | ||||
chr14:100833701-100833835 | Rare:23 | ||||
chr14:100897742-100897921 | Common:11; Rare:59 | ||||
chr15:23303467-23303779 | Rare:27 | ||||
chr15:29730407-29730611 | Rare:44 | ||||
chr15:41304112-41304187 | Rare:7 | ||||
chr15:48427678-48428033 | Rare:82; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr15:69415016-69415144 | Common:2; Rare:21 | ||||
chr15:71341738-71341919 | Rare:44 | ||||
chr15:82354933-82355170 | Rare:16 | ||||
chr16:12041688-12041815 | Common:1; Rare:35 | ||||
chr16:15715162-15715572 | Common:1; Rare:111; Clinvar:4; Clinvar (benign):8 | ||||
chr16:15719223-15719445 | Common:1; Rare:71; Clinvar:6; Clinvar (benign):3 |