chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225689398225689399CA28GENIChomozygous75247822
1225690219225690220AG24GENIChomozygous74731967
1225690781225690782AG24GENIChomozygous74731969
1225691366225691367GA29GENIChomozygous75247824
1225691506225691507CT26GENIChomozygous74731971
1225691991225691992AG10GENIChomozygous75247826
1225692140225692141TA24GENIChomozygous75247828
1225692272225692273GA29GENIChomozygous74731973
1225692512225692513TA20GENIChomozygous75247830
1225692619225692620GA23GENIChomozygous75247832
1225692986225692987TC24GENICpossibly homozygous74731979
1225693212225693213AG25GENIChomozygous75247834
1225693414225693415AT34GENIChomozygous75247836
1225693714225693715CT34GENIChomozygous75247838
1225693865225693866AG35GENIChomozygous74731981
1225694155225694156TG30GENIChomozygous74731983
1225694371225694372GA39GENIChomozygous75247840
1225694417225694418CT34GENIChomozygous75247842
1225694566225694567GA25GENIChomozygous75247844
1225695141225695142AG40GENIChomozygous75247846
1225695805225695806TC20GENIChomozygous75247848
1225696283225696284AG25GENIChomozygous75247850
1225696546225696547CG32GENIChomozygous75247852
1225696670225696671TC27GENIChomozygous75247854
1225697180225697181CT26GENIChomozygous75247856
1225698561225698562TC43GENIChomozygous75247860
1225700201225700202AG35GENICheterozygous74731989
1225702085225702086CT23GENIChomozygous75247866
1225707684225707685AC40GENIChomozygous75247870
1225708285225708286GA33GENIChomozygous75247872
1225708560225708561GA30GENIChomozygous75247874
1225709892225709893TA31GENIChomozygous75247876
1225710963225710964GA42GENIChomozygous75247878
1225711586225711587GA39GENIChomozygous75247880
1225712792225712793TG34GENIChomozygous74732003
1225712999225713000CA35GENIChomozygous75247882
1225714544225714545AG32GENIChomozygous74732005
1225735334225735335GA22GENIChomozygous75247884
1225739881225739882TC15GENIChomozygous74732027
1225733718225733719TC15GENICheterozygous77942473
1225788265225788266TA16GENICheterozygous75247886