chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2171170921711716CCCGCAT8GENICheterozygous132247343
X2171172221711723TA9GENICheterozygous132254422
X2171184721711847GT28GENIChomozygous129726947
X2171260621712607T22GENIChomozygous129726948
X2171529721715297T18GENIChomozygous129726949
X2171950421719505TC1GENIChomozygous132254423
X2172135021721351CG36GENIChomozygous108238330
X2171949221719493TA1GENIChomozygous131245355
X2172080121720802CT37GENIChomozygous108238326
X2172105321721054GC27GENIChomozygous108238328
X2172619921726199C3GENIChomozygous129726951
X2173260721732607T25GENICpossibly homozygous129726952
X2173323221733240TTTATTTA6GENICheterozygous129726953
X2173327021733276TATTTA6GENICheterozygous129726954
X2173334621733347GA17GENIChomozygous108238332
X2173534421735345TG19GENIChomozygous108238334
X2173874521738746CT34GENIChomozygous108238336
X2174534621745347T31GENIChomozygous129726955
X2175278521752785C27GENIChomozygous129726956
X2175280321752804G30GENIChomozygous129726957
X2175281921752820A27GENIChomozygous129726958
X2175283221752833A31GENIChomozygous129726959
X2175284821752849A31GENIChomozygous129726960
X2175285021752851C31GENIChomozygous129726961
X2175285621752858AA35GENIChomozygous129726962
X2175286621752867T33GENIChomozygous129726963
X2175286921752870C33GENIChomozygous129726964
X2175288221752882G32GENIChomozygous129726965
X2175292221752922C27GENIChomozygous129726966
X2175293321752934T25GENIChomozygous129726967
X2175315321753153A20GENIChomozygous129726972
X2174078021740781TC22GENIChomozygous108238338
X2174535821745359GA35GENIChomozygous108238340
X2174900721749008CT32GENIChomozygous108238342
X2175295721752957C26GENIChomozygous129726968
X2175297721752977C26GENIChomozygous129726969
X2175297921752979C25GENIChomozygous129726970
X2175314321753143C22GENIChomozygous129726971
X2173876421738765CT34GENIChomozygous108439628
X2175392121753922GA16GENICpossibly homozygous119909803
X2175405621754063GGGGAGG15GENIChomozygous129726973