chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51641978816419789AT66GENIChomozygous113673516
51642216216422163GA48GENIChomozygous113673518
51642251116422512GC46GENIChomozygous113673520
51642253916422540CA39GENICpossibly homozygous113673522
51642468616424687AC41GENIChomozygous113673524
51642630716426308TC16GENIChomozygous113673526
51642661116426612GA19GENIChomozygous113673528
51642667316426674CT20GENIChomozygous113673530
51642683316426834TG16GENICheterozygous113673532
51642695516426956GA23GENIChomozygous113673534
51642843516428436AG39GENIChomozygous113673536
51642845116428452AG34GENIChomozygous113673538
51642920516429206TA36GENIChomozygous113673540
51642937716429378GA58GENIChomozygous113673542
51642962516429626CT43GENIChomozygous113673544
51642981616429817CT34GENIChomozygous113673546
51643111216431113GT36GENIChomozygous113673548
51643206616432067AG25GENIChomozygous113673550
51643295716432958GA22GENIChomozygous113673552
51643378016433781GA58GENIChomozygous113673554
51643505516435056GA20GENICheterozygous113673556
51643524916435250GA35GENICheterozygous113673558
51643529216435293AG44GENICheterozygous113673560
51643550516435506GA42GENICheterozygous113673562
51643561616435617AG36GENICheterozygous113673564
51643561816435619AT36GENICheterozygous113673566
51643595016435951GA11GENICheterozygous113673568
51643748516437486AG29GENIChomozygous113673570
51643753316437534CT26GENIChomozygous113673572
51643794916437950AG36GENICpossibly homozygous113673574
51643808916438090GA46GENIChomozygous113673576
51643827216438273AG31GENIChomozygous113673578
51643843716438438AG42GENIChomozygous113673580
51643849816438499AG49GENIChomozygous113673582
51644278016442781TC38GENICpossibly homozygous113673584
51644357216443573CA35GENIChomozygous113673586
51644399616443997CT20GENIChomozygous113673588
51644433916444340AT22GENIChomozygous113673590
51644481416444815TC27GENIChomozygous113673592
51644509416445095AC49GENIChomozygous113673594
51644535916445360GA47GENIChomozygous113673596
51644644616446447GA39GENIChomozygous113673598