chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142819455142819456TC30GENIChomozygous115942480
7142821555142821556TC35GENIChomozygous115942481
7142823002142823003GA33GENIChomozygous116098674
7142823135142823136CT35GENIChomozygous115942483
7142823641142823642CT30GENIChomozygous115942485
7142823916142823917GA44GENIChomozygous115942486
7142824186142824187CT33GENIChomozygous115942487
7142825311142825312CT24GENIChomozygous115942488
7142826399142826400CT21GENIChomozygous115942489
7142826985142826986TC28GENIChomozygous115942490
7142827057142827058AT29GENIChomozygous115942491
7142827264142827265TC53GENIChomozygous115942493
7142827310142827311AC40GENIChomozygous115942495
7142827419142827420GT25GENIChomozygous115942496
7142827763142827764AG23GENICpossibly homozygous115942497
7142838888142838889GA21GENIChomozygous115942507
7142839765142839766GA28GENIChomozygous115942508
7142839890142839891CT15GENIChomozygous115942509
7142843862142843863AG26GENIChomozygous115942517
7142844647142844648TC37GENIChomozygous115942518
7142845070142845071GA21GENIChomozygous115942519
7142845652142845653CT36GENIChomozygous115942520
7142845755142845756CA39GENIChomozygous115942521
7142845908142845909GA36GENIChomozygous115942522
7142845988142845989GA31GENIChomozygous115942523
7142846107142846108CG36GENIChomozygous115942524
7142846294142846295GA29GENIChomozygous115942525
7142847205142847206AG41GENIChomozygous115942526
7142847900142847901CT32GENIChomozygous115942527
7142849608142849609TC31GENIChomozygous115942528
7142853531142853532GA24GENIChomozygous115942533
7142854060142854061TC34GENIChomozygous115942534
7142854458142854459GA16GENIChomozygous115942535
7142858078142858079TC29GENIChomozygous115942538