chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1458487755848776GA26GENIChomozygous113571164
1458490205849021AG29GENIChomozygous113802338
1458491605849161AT29GENIChomozygous113571165
1458493045849305AG23GENIChomozygous118671621
1458494455849446AC24GENIChomozygous113802340
1458497485849749AG23GENIChomozygous113571166
1458497495849750CA23GENIChomozygous113571167
1458497535849754AG23GENIChomozygous113712569
1458498725849873CT25GENIChomozygous118671625
1458498855849886AG19GENIChomozygous118671627
1458499095849910TC18GENIChomozygous113802342
1458503145850315GT17GENIChomozygous118778167
1458492715849272CG16GENIChomozygous118778164
1458502475850248TC21GENIChomozygous118778165
1458503135850314CT17GENIChomozygous118778166
1458498535849854CG26GENIChomozygous113322668
1458505225850523GC6GENIChomozygous118671631
1458505555850556TC4GENIChomozygous118778168
1458511525851153AC8GENICpossibly homozygous118778169
1458516485851649CT23GENICheterozygous118671637
1458516555851656TC25GENICheterozygous118778170
1458517545851755CG36GENIChomozygous113802345
1458517775851778GA43GENICheterozygous118778171
1458517795851780GC44GENICheterozygous118778172
1458518305851831AG44GENICheterozygous118778173
1458523615852362GA22GENICheterozygous118778174
1458523895852390TA20GENICheterozygous118778175
1458526395852640TG25GENICpossibly homozygous118778176
1458536065853607GA44GENICheterozygous118778177
1458536995853700CT32GENICheterozygous118778178
1458537025853703AG32GENICheterozygous118778179
1458537625853763GA40GENICheterozygous118778180
1458582715858272CT14GENIChomozygous118778181
1458584425858443TC15GENIChomozygous118778182
1458585585858559AG22GENIChomozygous118778183
1458592805859281TC17GENIChomozygous118778184
1458592815859282GA17GENIChomozygous118778185
1458594115859412TC15GENIChomozygous118778186