chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187162054187162055CG29GENICpossibly homozygous110166988
2187162200187162201TA25GENIChomozygous111278050
2187162356187162357TC23GENIChomozygous111278052
2187162932187162933GA23GENIChomozygous111278054
2187163386187163387AT23GENIChomozygous110803641
2187163719187163720TC30GENIChomozygous110803642
2187163833187163834AG21GENICpossibly homozygous110803643
2187164064187164065TG21GENIChomozygous110166992
2187164868187164869TC26GENIChomozygous110166993
2187164913187164914GA30GENIChomozygous111278056
2187165065187165066AG28GENIChomozygous110166994
2187165764187165765GA56GENIChomozygous110803645
2187166445187166446CT24GENIChomozygous111278058
2187167375187167376AC24GENIChomozygous110166995
2187167603187167604AG38GENIChomozygous110166997
2187168259187168260GA18GENIChomozygous111278060
2187168914187168915AG19GENIChomozygous110166998
2187169697187169698TG20GENIChomozygous110167001
2187170415187170416AG27GENICpossibly homozygous111278062
2187170663187170664AC17GENIChomozygous110167002
2187171916187171917AG34GENIChomozygous110167004
2187172861187172862AG16GENIChomozygous110167005
2187173979187173980CT23GENIChomozygous111278064
2187176239187176240TC18GENIChomozygous110167010
2187177411187177412GA13GENIChomozygous111278065
2187179339187179340CT23GENIChomozygous111278067
2187179800187179801TC20GENIChomozygous110167016
2187180011187180012TC18GENIChomozygous110167017
2187180169187180170AT26GENIChomozygous110167020
2187181292187181293AG29GENIChomozygous110167025