chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87737139277371393CCT8GENICheterozygous745705608
87737139377371394T-8GENICheterozygous745705607
87740427877404279TC9GENICheterozygous631576316
87743231377432314GGC4GENIChomozygous745705614
87744212177442122A-16GENICheterozygous745705616
87745630477456305CA21GENICheterozygous631576317
87745638777456388GT18GENICheterozygous631576318
87746786777467868TG7GENICheterozygous631576319
87749444677494447GA13GENIChomozygous631576320
87749546977495470CCT8GENIChomozygous745705617
87751397177513972AATT14GENIChomozygous745705619
87752398377523984G-9GENICheterozygous745705620
87753576277535763A-6GENICheterozygous745705621
87753881077538811CCT3GENICheterozygous745705624
87756135577561356T-3GENICheterozygous745705626
87756525477565255A-2GENICheterozygous745705627
87756838677568387GGACACACAC2GENIChomozygous745705630
87759392077593921AAATC14GENICpossibly homozygous745705631
87761016677610167T-2GENICheterozygous745705632
87761794277617943GGT6GENIChomozygous745705633
87761981577619816G-6GENIChomozygous745705634
87762301177623012CCAA14GENIChomozygous745705635
87763371377633714T-2GENICheterozygous745705636
87763837377638383AAATGGGGGA----------3GENIChomozygous745705637
87765180477651805AAAAAG5GENICheterozygous745705638
87765516277655163A-4GENICheterozygous745705639
87767637277676373TTA1GENIChomozygous745705640
87769536477695365TG6GENICheterozygous631576321
87771838977718390GGT1GENIChomozygous745705644
87774816877748169A-4GENICheterozygous745705645
87774828877748289A-1GENIChomozygous745705646
87775250177752502TTA1GENIChomozygous745705647
87775462277754623AAG2GENIChomozygous745705648
87776383877763839G-7GENICheterozygous745705649