Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42980394-42980571 | Common:1; Rare:53 | ||||
chr17:43125359-43125654 | Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170243-43170374 | Rare:32 | ||||
chr17:43170982-43171245 | Rare:85 | ||||
chr17:43778917-43779078 | Rare:36 | ||||
chr17:43833114-43833362 | Common:2; Rare:70 | ||||
chr17:43847053-43847176 | Rare:28 | ||||
chr17:44123596-44123834 | Common:3; Rare:70 | ||||
chr17:44186663-44187002 | Common:1; Rare:123 | ||||
chr17:44220845-44220986 | Rare:39 | ||||
chr17:44324760-44324977 | Common:2; Rare:80 | ||||
chr17:44503367-44503658 | Rare:122 | ||||
chr17:44899375-44899741 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
chr17:45060992-45061339 | Common:2; Rare:91 | ||||
chr17:45148159-45148496 | Common:1; Rare:107 |