chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63205886232058863GA26GENIChomozygous54330873
63205915132059152AG30GENIChomozygous54330876
63205950832059509GA26GENIChomozygous54330879
63205961432059615GA48GENIChomozygous54330882
63206125932061260CCAA20GENICpossibly homozygous54330886
63206125932061260CCA20GENICheterozygous55490628
63206244632062447CT31GENIChomozygous54330892
63206313632063137GA45GENIChomozygous54330895
63206343732063438CCT37GENIChomozygous54330898
63206609632066098TT--30GENIChomozygous54330901
63206651232066513GA58GENIChomozygous54330904
63206699432066995GA29GENIChomozygous54330906
63206740832067409TC40GENIChomozygous54330911
63206883332068837ACAC----6GENICheterozygous54330914
63206883532068837AC--6GENICheterozygous54330917
63206906432069065GT28GENIChomozygous54330920
63206910832069109GA25GENIChomozygous54330923
63206956232069563CCCA19GENIChomozygous54330925
63206998732069988GA44GENIChomozygous54330928
63207068632070687AATTT24GENICheterozygous54330931
63207068632070687AATT24GENICheterozygous54330934
63207068632070687AAT24GENICheterozygous55698749
63207261832072619CCTTTTTTTT2GENIChomozygous55490638
63207473732074745TTCTTTCT--------20GENIChomozygous54330940
63207503932075040CT39GENIChomozygous54330946
63207520032075201AG40GENIChomozygous54330948
63207646032076461AG40GENIChomozygous54330951
63207653732076538CT42GENIChomozygous54330955
63207683032076831GC39GENIChomozygous54330958
63207687032076874AATG----33GENIChomozygous54330960
63207881632078817CA34GENIChomozygous54330963
63207919132079192TA21GENIChomozygous54330966
63207946132079462CT36GENIChomozygous54330969
63207983332079834GA33GENIChomozygous54330972
63207998832079989GA48GENIChomozygous54330975
63208079932080800GA23GENIChomozygous54330978