chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG50GENICpossibly homozygous533804535
1228739709228739710AG53GENIChomozygous536817337
1228739864228739868CCCC----7GENIChomozygous695128423
1228741235228741236GT29GENIChomozygous536817338
1228741277228741278T-17GENICheterozygous695128424
1228741329228741330AAGAGAG16GENIChomozygous695128425
1228741505228741506A-14GENIChomozygous695128426
1228741525228741526A-17GENIChomozygous695128427
1228741661228741662TG43GENICheterozygous536817339
1228741819228741820CCG32GENIChomozygous695128428
1228743588228743589TG33GENICheterozygous536817340
1228744220228744221TC45GENICpossibly homozygous536817341
1228744784228744785TG26GENICheterozygous536817342
1228745418228745419CT54GENIChomozygous536817343
1228746722228746723TC47GENIChomozygous536817344
1228747028228747043CTGGCATTGTGGTAG---------------17GENIChomozygous695128429
1228751732228751733CCATTT4GENIChomozygous695128430
1228752487228752488AG34GENIChomozygous536817345
1228752836228752837G-31GENIChomozygous695128431
1228753035228753036CCCACA14GENICpossibly homozygous695128432
1228753085228753089ACAC----18GENIChomozygous695128433
1228754008228754009T-27GENIChomozygous695128435
1228754121228754122AG19GENICheterozygous536817346
1228754285228754286CCT14GENICheterozygous695128436
1228754312228754313AT27GENICheterozygous536817347
1228755144228755145CT32GENIChomozygous536817348
1228755467228755468GGCA33GENICpossibly homozygous695128437
1228755487228755488T-44GENICheterozygous695128438
1228755487228755488TTAC35GENICheterozygous695128440
1228755487228755488TTACAC35GENICpossibly homozygous695128441
1228755506228755507TA53GENICheterozygous536817349
1228756439228756440CCT8GENICheterozygous695128442
1228756440228756441T-8GENICheterozygous695128443
1228756521228756522AAGT4GENICheterozygous695128444