Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:23105687-23105839 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):3 | ||||
chr7:26201571-26201821 | Common:2; Rare:131 | ||||
chr7:27095998-27096125 | Rare:36 | ||||
chr7:27113826-27113954 | Rare:30 | ||||
chr7:27185143-27185433 | Common:1; Rare:98 | ||||
chr7:27740097-27740199 | Common:3; Rare:27 | ||||
chr7:30594735-30595113 | Common:6; Rare:175; Clinvar:9; Clinvar (benign):14 | ||||
chr7:33109363-33109513 | Rare:56; Clinvar:1 | ||||
chr7:35695160-35695251 | Common:1; Rare:34 | ||||
chr7:40134588-40134648 | Rare:22 | ||||
chr7:41700586-41700775 | Rare:22 | ||||
chr7:42932160-42932404 | Rare:99 | ||||
chr7:44582212-44582553 | Common:1; Rare:126 | ||||
chr7:44796413-44796688 | Common:2; Rare:97 | ||||
chr7:44999922-45000210 | Common:1; Rare:59 |