chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1458486345848635AG20GENIChomozygous809153963
1458487755848776GA48GENIChomozygous809153964
1458490205849021AG64GENIChomozygous809153965
1458491605849161AT66GENIChomozygous809153966
1458492715849272CG37GENICpossibly homozygous809153967
1458493045849305AG43GENICpossibly homozygous809153968
1458494455849446AC31GENIChomozygous809153969
1458497485849749AG41GENICpossibly homozygous809153970
1458497495849750CA40GENICpossibly homozygous809153971
1458497535849754AG42GENIChomozygous809153972
1458498535849854CG35GENIChomozygous809153973
1458498725849873CT31GENIChomozygous809153974
1458498855849886AG33GENIChomozygous809153975
1458499095849910TC37GENIChomozygous809153976
1458502475850248TC43GENIChomozygous809153977
1458503135850314CT45GENIChomozygous809153978
1458503145850315GT43GENIChomozygous809153979
1458505555850556TC16GENICheterozygous809153980
1458506405850641CT33GENICheterozygous809153981
1458511525851153AC39GENICheterozygous809153982
1458516485851649CT40GENICheterozygous809153983
1458516555851656TC46GENICheterozygous809153984
1458517545851755CG99GENIChomozygous809153985
1458517775851778GA97GENICheterozygous809153986
1458517795851780GC97GENICheterozygous809153987
1458518305851831AG79GENICheterozygous809153988
1458518815851882GT55GENICheterozygous809153989
1458523615852362GA59GENICheterozygous809153990
1458523895852390TA52GENICheterozygous809153991
1458525095852510CG32GENICheterozygous809153992
1458526395852640TG35GENICheterozygous809153993
1458535145853515AC46GENICheterozygous809153994
1458536065853607GA108GENICheterozygous809153995
1458536995853700CT66GENICheterozygous809153996
1458537025853703AG60GENICheterozygous809153997
1458537625853763GA64GENICheterozygous809153998
1458584425858443TC22GENIChomozygous809153999
1458585585858559AG29GENIChomozygous809154000
1458592805859281TC42GENIChomozygous809154001
1458592815859282GA42GENICpossibly homozygous809154002
1458594115859412TC42GENIChomozygous809154003