chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101848572818485729GA26GENIChomozygous116995556
101848616218486163GA17GENIChomozygous116995557
101848985818489859GT16GENIChomozygous116995558
101849012118490122CT15GENIChomozygous116995559
101849050118490502GA33GENIChomozygous116995560
101849077918490780AG12GENIChomozygous116503057
101849088618490887GA33GENIChomozygous116503059
101849096718490968GT24GENIChomozygous116503061
101849172418491725GA24GENIChomozygous116503063
101849228418492285GA32GENIChomozygous116740591
101849238818492389TC37GENIChomozygous116740592
101849241618492417CT32GENIChomozygous116995561
101849368918493690TC12GENIChomozygous116503073
101849591718495918AG32GENIChomozygous116503075
101849619418496195CT17GENIChomozygous116995562
101849630518496306TA34GENIChomozygous116503077
101849817818498179AG19GENIChomozygous116995563
101849831418498315TG20GENIChomozygous116503079
101849951018499511AG17GENIChomozygous116995564
101850079218500793CT10GENIChomozygous116861344
101850079318500794TC10GENIChomozygous116861346
101850128218501283AC10GENIChomozygous116918860
101850133918501340GT6GENIChomozygous116918862
101850155118501552AT19GENIChomozygous116503085
101850429118504292CG23GENIChomozygous116995565
101850463418504635CG22GENIChomozygous116503121
101850475718504758TC24GENIChomozygous116503125
101850766118507662GA10GENIChomozygous116995566
101850904618509047CG13GENIChomozygous116995567
101850914318509144AG25GENIChomozygous116995568
101850947618509477TA16GENIChomozygous116995569