Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1713910-1713979 | Rare:11 | ||||
chr17:3665155-3665378 | Common:11; Rare:52 | ||||
chr17:8222590-8222679 | Common:2; Rare:20 | ||||
chr17:44351456-44351669 | Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
chr17:50199226-50199577 | Common:1; Rare:115; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr17:64975575-64975810 | Common:2; Rare:91 | ||||
chr17:75038684-75038908 | Common:3; Rare:39 | ||||
chr17:76557681-76557815 | Rare:49 | ||||
chr18:5237984-5238163 | Common:1; Rare:64 | ||||
chr18:12367048-12367332 | Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
chr19:19492327-19492625 | Rare:111 | ||||
chr19:43508029-43508211 | Rare:50 | ||||
chr19:45767443-45767748 | Rare:90 | ||||
chr19:46608954-46609148 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr19:46860822-46861111 | Common:3; Rare:93 |