Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:9435490-9435641 | Common:1; Rare:58 | ||||
chr19:9538563-9538736 | Common:1; Rare:56 | ||||
chr19:9621192-9621562 | Common:3; Rare:105 | ||||
chr19:9675018-9675202 | Common:2; Rare:51 | ||||
chr19:9768559-9768785 | Common:2; Rare:80 | ||||
chr19:9786042-9786206 | Rare:45 | ||||
chr19:9818816-9818858 | Rare:17 | ||||
chr19:9827838-9827982 | Common:1; Rare:53 | ||||
chr19:9835012-9835354 | Rare:139 | ||||
chr19:10271040-10271127 | Rare:23 | ||||
chr19:10315986-10316276 | Common:2; Rare:88; Clinvar (benign):5 | ||||
chr19:10333503-10333709 | Rare:66 | ||||
chr19:10836272-10836551 | Common:2; Rare:71 | ||||
chr19:10928551-10928751 | Common:1; Rare:50 | ||||
chr19:11089297-11089551 | Rare:53; Clinvar:12; Clinvar (pathogenic):1 |