chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
193760390337603904CT13GENIChomozygous109693968
193760789337607894TC28GENIChomozygous109693970
193760953637609537CA15GENIChomozygous109693972
193760996537609966AT16GENIChomozygous109693974
193761148037611481AG20GENIChomozygous109693976
193761206937612070AG13GENIChomozygous110065523
193761253237612533CT28GENIChomozygous109693978
193761312737613128GT30GENIChomozygous109693980
193761477837614779AG30GENIChomozygous109693982
193761636537616366AG17GENIChomozygous109693984
193761743737617438TC34GENIChomozygous109693986
193761989937619900CG26GENIChomozygous109693988
193762176237621763AG20GENIChomozygous109693996
193762292237622923TC14GENIChomozygous109694000
193762459437624595GT30GENIChomozygous109694002
193762459837624599TC30GENIChomozygous109694004
193762460137624602GA30GENIChomozygous109694006
193762763237627633GT17GENIChomozygous109694008
193762879737628798GA20GENIChomozygous109694010
193762962437629625TG14GENIChomozygous109694012
193762974237629743GC22GENIChomozygous109694014
193763021237630213CT21GENIChomozygous109924814
193763059637630597TA27GENIChomozygous109694016
193763213437632135TG31GENIChomozygous109694019
193763333437633335AT31GENIChomozygous109694021
193763407037634071CT25GENIChomozygous109694023
193763412237634123GC22GENIChomozygous109694025
193763437037634371CT24GENIChomozygous109924816
193763442637634427AG21GENIChomozygous109694027
193763624237636243AG29GENIChomozygous109694029
193763681537636816TG17GENIChomozygous109694031
193763863537638636TG28GENIChomozygous109694033
193764104237641043AC30GENIChomozygous109694035
193764178137641782TC46GENIChomozygous109694037
193764255637642557AG18GENIChomozygous109694039
193764256637642567AG17GENIChomozygous109924818
193764505337645054CA21GENIChomozygous109694043
193764722837647229TC15GENIChomozygous109694045
193764902037649021AG20GENIChomozygous109694047
193761051237610513TC6GENIChomozygous109976874
193761013937610140GA22GENIChomozygous109780951
193761050537610506CT5GENIChomozygous109961690