chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116581664116581665AG64GENIChomozygous53721428
8116582097116582098A-9GENIChomozygous53291240
8116583144116583145GT36GENIChomozygous52828382
8116583369116583370AG25GENIChomozygous52828383
8116584154116584158GTTC----9GENICheterozygous53411376
8116584195116584196AG15GENIChomozygous52828384
8116584398116584399TC39GENIChomozygous52828385
8116584906116584907AAT32GENIChomozygous53305828
8116586144116586145GGC26GENIChomozygous52828399
8116586493116586494CT31GENIChomozygous53721430
8116586709116586713CACC----20GENICheterozygous53634433
8116587456116587457TA31GENIChomozygous52828405
8116587622116587623GA22GENIChomozygous53721432
8116587624116587625AC22GENIChomozygous52828406
8116587734116587736AA--6GENICheterozygous53305833
8116587970116587971GA52GENIChomozygous53721434
8116588490116588492AT--30GENICpossibly homozygous52828410
8116588494116588498ACAA----36GENICheterozygous53411381
8116588496116588498AA--29GENICheterozygous52828411
8116588541116588542AG37GENIChomozygous53051533
8116588600116588606TTTTTT------5GENICheterozygous53523578
8116588601116588606TTTTT-----5GENICheterozygous53523580
8116589652116589653GA15GENIChomozygous53721436
8116591285116591286AG54GENIChomozygous53051537
8116592100116592101AATTT23GENIChomozygous53721438
8116593096116593097TC30GENIChomozygous53051541
8116593101116593102GA34GENIChomozygous53721440
8116595831116595855CTGCCTCCGCCTCTGCCTCCGCCT------------------------7GENIChomozygous53411382
8116586970116586971AAGTGTGT8GENICheterozygous53982644
8116586173116586174C-14GENIChomozygous53982642