chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130192683130192683A36GENIChomozygous149353842
7130192745130192745GT45GENIChomozygous149353843
7130192821130192822GA50GENIChomozygous138223921
7130193469130193470TC51GENIChomozygous138223923
7130194050130194051CT42GENIChomozygous148730200
7130194278130194278AAAGATTTCACATTTAAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGACCCCAGCACCGGGGGGGGGAAAAAAAAAA19GENICpossibly homozygous149353844
7130194511130194512CT34GENIChomozygous148730201
7130195326130195327CT62GENIChomozygous148730202
7130197200130197201CT58GENIChomozygous148730203
7130196367130196368TA56GENIChomozygous149359486
7130198452130198453TG61GENIChomozygous146460010
7130198993130198994AC58GENIChomozygous146460012