chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154478692154478693TG16GENIChomozygous108317312
1154478821154478822GA17GENIChomozygous108317314
1154479672154479673AG19GENIChomozygous108317316
1154479938154479939CA28GENIChomozygous108317317
1154480020154480021TG23GENICpossibly homozygous108317319
1154480796154480797CT25GENIChomozygous108317321
1154482018154482019TC14GENIChomozygous108317329
1154482769154482770AG10GENIChomozygous108317331
1154482773154482774TC10GENIChomozygous108317333
1154483272154483273CT12GENIChomozygous108317335
1154483837154483838AG13GENIChomozygous108317337
1154483840154483841CT17GENIChomozygous108317339
1154484208154484209CG15GENIChomozygous108317341
1154484727154484728GA12GENIChomozygous108317343
1154485208154485209AG20GENIChomozygous108317345
1154485627154485628TC13GENIChomozygous108317347
1154485706154485707GA16GENIChomozygous108317349
1154486088154486089GA23GENIChomozygous108317351
1154486444154486445TC6GENIChomozygous108317353
1154494593154494594GA16GENIChomozygous125293494
1154481733154481734GA14GENIChomozygous109151243
1154493089154493090GA11GENICheterozygous125464066
1154495192154495193CT16GENIChomozygous125464067
1154496926154496927GA18GENIChomozygous108317359
1154497041154497042TG8GENIChomozygous109151251
1154497243154497244TC21GENIChomozygous108317363
1154500637154500638AG9GENIChomozygous108317368
1154501972154501973GA23GENIChomozygous108317370
1154502301154502302CT18GENIChomozygous109151257
1154502986154502987CT13GENIChomozygous108317376
1154506183154506184GT20GENIChomozygous108317380
1154506593154506594TC9GENIChomozygous108317382