chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139840228898402292ACAC----9GENICheterozygous736377633
139840229098402292AC--9GENICpossibly homozygous736377634
139840273998402740GGTT2GENIChomozygous736377636
139840291398402914CT19GENIChomozygous612600303
139840331998403323TTTT----4GENICheterozygous736377637
139840332298403323T-4GENICheterozygous736377638
139840619398406194TTTTTG13GENIChomozygous736377639
139840632598406326TC21GENIChomozygous612600304
139840655398406554TC32GENIChomozygous612600305
139840693198406932G-2GENIChomozygous736377640
139840693898406939C-2GENIChomozygous736377641
139840787298407873AG35GENIChomozygous615708540
139840791798407918CT30GENIChomozygous612600306
139840792998407930TC37GENIChomozygous612600307
139840800798408008G-37GENIChomozygous736377642
139840924698409247AG34GENIChomozygous612600308
139840972298409723CT36GENIChomozygous612600309
139841027898410279AG23GENIChomozygous615708541
139841201398412018TTAAC-----24GENIChomozygous736377643
139841227698412277CCTTT16GENICheterozygous736377646
139841242598412426CCT20GENICpossibly homozygous736377647
139841329198413292AG21GENIChomozygous612600310
139841379498413795TG32GENIChomozygous612600311
139841427898414279A-5GENIChomozygous736377649
139841472398414724AAT10GENICheterozygous736377651
139841472398414724AATTTTTT10GENICheterozygous736377652
139841534898415349CT35GENIChomozygous612600312
139841708498417085AAT40GENIChomozygous736377653
139841708598417086AATATTT41GENIChomozygous736377654
139841709398417094TTATATATA40GENIChomozygous736377657
139841771198417712GC24GENIChomozygous612600313
139841855398418554T-20GENIChomozygous736377658
139841858998418590CG32GENIChomozygous612600314
139841887098418871GA21GENIChomozygous612600315
139842142698421427GC38GENIChomozygous612600316
139842193698421937GC39GENIChomozygous612600317
139842735298427353GT22GENIChomozygous612600318