chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124069726540697266A-8GENIChomozygous50543733
124069750540697509ACAC----5GENIChomozygous50543734
124069875040698751TC28GENIChomozygous50204351
124070197840701979CCA19INTERGENIChomozygous50204363
124070198240701983T-19INTERGENIChomozygous50204364
124070198440701985TC19INTERGENIChomozygous50204365
124070202540702026CCA3INTERGENICheterozygous50204366
124070245340702454TTA12INTERGENIChomozygous50204370
124070246340702464TTAA14INTERGENIChomozygous50422917
124069797240697973GA27GENIChomozygous50422914
124069932740699328CG26GENIChomozygous50422915
124069995040699956GAGGGG------6INTERGENIChomozygous50422916
124070246840702469GA14INTERGENIChomozygous50543735
124070390540703906TA28INTERGENIChomozygous50422918
124070433040704331TG45INTERGENIChomozygous50422919
124070441340704414GA27INTERGENIChomozygous50204375
124070457640704577CT25INTERGENIChomozygous50422920
124070487740704878G-6INTERGENIChomozygous50204376
124070720640707207TTC27INTERGENIChomozygous50422921
124070746340707464GA39INTERGENIChomozygous50422922
124070760540707606CT40INTERGENIChomozygous50422923
124070762240707623GA32INTERGENIChomozygous50422924
124070787040707871AATAGC11INTERGENIChomozygous50422926
124070814240708143CCA21INTERGENIChomozygous50422927
124070878340708784GC26INTERGENIChomozygous50422928
124070878440708785AC25INTERGENIChomozygous50422929
124070883240708833TTTTTTTTG9INTERGENICpossibly homozygous50543736
124070884540708846GT11INTERGENIChomozygous50543737
124070894140708942TC27INTERGENICpossibly homozygous50422930
124070910040709101TC25INTERGENIChomozygous50204379
124070925440709255CT17INTERGENIChomozygous50422931
124070883540708836CT13INTERGENIChomozygous50512453