chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118804936588049366CG17GENIChomozygous118212184
118805641488056415GA22GENICpossibly homozygous115929716
118805937988059380AG12GENIChomozygous118171602
118806075888060759GA40GENIChomozygous116110829
118806330988063310AG37GENIChomozygous115929726
118806600188066002TC33GENIChomozygous115929730
118807100888071009TC41GENIChomozygous115929736
118807141788071418TC15GENICpossibly homozygous118212185
118807257488072575GT62GENIChomozygous116251134
118807524788075248TA42GENIChomozygous115929740
118807747788077478TC22GENIChomozygous115929742
118807907888079079GA36GENIChomozygous115929744
118807971688079717CG48GENIChomozygous116397966
118806617788066178GA40GENICpossibly homozygous116397961
118806623188066232CT29GENIChomozygous116397962
118806801488068015GA34GENIChomozygous116397963
118807414088074141AG46GENIChomozygous116397964
118807801688078017AG32GENIChomozygous116397965
118807795888077959AG42GENIChomozygous116107432
118808087988080880GT44GENICpossibly homozygous115929748
118808184988081850GA45GENIChomozygous116397967
118808237588082376CT54GENICpossibly homozygous116397968
118808274488082745GA34GENIChomozygous116397969
118808352188083522GA34GENIChomozygous115929752
118808363888083639AG34GENICpossibly homozygous115929754
118808498888084989GA29GENICpossibly homozygous118212186
118808731088087311GT22GENIChomozygous115929758
118808781488087815GA34GENIChomozygous116397970