chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1617144116171442CT11GENIChomozygous108472953
X1617154116171542CT11GENIChomozygous108472955
X1617314816173149GA14GENIChomozygous108370738
X1617342816173429TC19GENIChomozygous108370740
X1617347916173480AG15GENIChomozygous108370742
X1617363416173635TA4GENIChomozygous108472957
X1617409316174094CG8GENIChomozygous108472959
X1617462916174630GA27GENIChomozygous108472961
X1617505816175059TA8GENIChomozygous108233628
X1617618716176188TC8GENIChomozygous108472963
X1617680916176810TC10GENIChomozygous108472965
X1617803316178034GA14GENIChomozygous108472967
X1617956616179567TA12GENIChomozygous108370744
X1617991516179916AG9GENIChomozygous108370746
X1618104116181042GA9GENIChomozygous108472969
X1618137216181373AT13GENIChomozygous108370752
X1618198016181981CG5GENIChomozygous108370754
X1618400216184003GA7GENIChomozygous108472971
X1618409416184095AG11GENIChomozygous108370756
X1618711616187117AC11GENIChomozygous108472973
X1618813516188136GA5GENIChomozygous108370762
X1618813616188137AT5GENIChomozygous108370764
X1618872816188729CA20GENIChomozygous108370766
X1618874316188744CT22GENIChomozygous108472975
X1618889916188900TC17GENIChomozygous108370768
X1618947516189476TG8GENIChomozygous108370770
X1618971616189717CT15GENIChomozygous108370772
X1619008416190085CT13GENIChomozygous108370774
X1619049116190492TC15GENIChomozygous108370776
X1619091916190920CA16GENIChomozygous108472977
X1619096516190966CT7GENIChomozygous108370780
X1619138916191390GA10GENIChomozygous108370782
X1619163716191638TC8GENIChomozygous108370784
X1619185216191853AG9GENIChomozygous108472979
X1619188316191884CT13GENIChomozygous108370786
X1619205716192058AG6GENIChomozygous108370788
X1619305016193051TC18GENIChomozygous108370792
X1619316416193165AG11GENIChomozygous108370794
X1619568716195688AG8GENIChomozygous108233630