chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X8409994084099941TC13GENIChomozygous108281377
X8410378984103790GT8GENIChomozygous108397228
X8410544084105441AG18GENIChomozygous108281383
X8410773884107739CG9GENIChomozygous108281385
X8410792784107928TC16GENIChomozygous108397230
X8411143184111432CT6GENIChomozygous125126130
X8411146084111461CG6GENIChomozygous125107298
X8411149184111492CG12GENIChomozygous125107299
X8411150684111507TG10GENIChomozygous108281391
X8411150784111508GT10GENIChomozygous108281393
X8411258384112584GT17GENIChomozygous108397232
X8411321984113220AG17GENIChomozygous108281397
X8411427184114272CT20GENICpossibly homozygous108281399
X8411459584114596TC18GENIChomozygous108281401
X8411503384115034TC16GENICheterozygous108281403
X8411882284118823CT9GENIChomozygous108397234
X8411929884119299AG20GENIChomozygous108281413
X8412000084120001TC16GENIChomozygous108281417
X8412290584122906TC20GENIChomozygous108281425
X8412294884122949TG14GENIChomozygous108281427
X8412893584128936TC12GENIChomozygous108397236
X8413179784131798GT11GENIChomozygous108397238
X8413242284132423CG15GENIChomozygous108281441
X8413320984133210TC13GENIChomozygous108397240
X8413452684134527AT17GENIChomozygous108397244
X8413481484134815CT26GENIChomozygous108397250
X8414262384142624AC22GENIChomozygous108281447
X8414427984144280CA20GENIChomozygous108397254
X8414546484145465AG15GENIChomozygous108397256
X8414759984147600TC13GENIChomozygous108281451
X8414809784148098GT11GENIChomozygous108397258
X8414826984148270GA28GENIChomozygous108397260
X8414855684148557CT5GENIChomozygous120055903
X8415089084150891CT22GENIChomozygous108397262
X8415257584152576AT22GENIChomozygous108397264
X8415935384159354AG8GENIChomozygous108281462
X8415937884159379AT7GENIChomozygous108397266
X8416054784160548GA7GENIChomozygous108281464
X8416501284165013AT15GENIChomozygous108397268
X8416512984165130GA12GENIChomozygous108397270
X8411629884116299GA15GENIChomozygous108450802