chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1458487755848776GA26GENIChomozygous786791506
1458490205849021AG29GENIChomozygous786791507
1458491605849161AT29GENIChomozygous786791508
1458492715849272CG16GENIChomozygous786791509
1458493045849305AG23GENIChomozygous786791510
1458494455849446AC24GENIChomozygous786791511
1458497485849749AG23GENIChomozygous786791512
1458497495849750CA23GENIChomozygous786791513
1458497535849754AG23GENIChomozygous786791514
1458498535849854CG26GENIChomozygous786791515
1458498725849873CT25GENIChomozygous786791516
1458498855849886AG19GENIChomozygous786791517
1458499095849910TC18GENIChomozygous786791518
1458502475850248TC21GENIChomozygous786791519
1458503135850314CT17GENIChomozygous786791520
1458503145850315GT17GENIChomozygous786791521
1458505225850523GC6GENIChomozygous786791522
1458505555850556TC4GENIChomozygous786791523
1458511525851153AC8GENICpossibly homozygous786791524
1458516485851649CT23GENICheterozygous786791525
1458516555851656TC25GENICheterozygous786791526
1458517545851755CG36GENIChomozygous786791527
1458517775851778GA43GENICheterozygous786791528
1458517795851780GC44GENICheterozygous786791529
1458518305851831AG44GENICheterozygous786791530
1458523615852362GA22GENICheterozygous786791531
1458523895852390TA20GENICheterozygous786791532
1458526395852640TG25GENICpossibly homozygous786791533
1458536065853607GA44GENICheterozygous786791534
1458536995853700CT32GENICheterozygous786791535
1458537025853703AG32GENICheterozygous786791536
1458537625853763GA40GENICheterozygous786791537
1458582715858272CT14GENIChomozygous786791538
1458584425858443TC15GENIChomozygous786791539
1458585585858559AG22GENIChomozygous786791540
1458592805859281TC17GENIChomozygous786791541
1458592815859282GA17GENIChomozygous786791542
1458594115859412TC15GENIChomozygous786791543