Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41812841-41813010 | Rare:43; Clinvar:2 | ||||
chr17:41966610-41966819 | Common:1; Rare:74 | ||||
chr17:42017390-42017711 | Common:1; Rare:107 | ||||
chr17:42577664-42577845 | Rare:88 | ||||
chr17:42609333-42609732 | Common:8; Rare:165; Clinvar (benign):2 | ||||
chr17:42773394-42773491 | Rare:31 | ||||
chr17:42833341-42833479 | Rare:51 | ||||
chr17:42964417-42964503 | Rare:37 | ||||
chr17:43125357-43125642 | Rare:62; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170303-43170394 | Rare:16 | ||||
chr17:43171010-43171245 | Rare:74 | ||||
chr17:43545897-43546073 | Common:2; Rare:28 | ||||
chr17:43546299-43546647 | Common:2; Rare:80 | ||||
chr17:43778917-43779078 | Rare:36 | ||||
chr17:44186691-44187030 | Rare:111 |