chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51641371516413716GA16GENIChomozygous118870390
51641409416414095GT19GENIChomozygous118870393
51641510416415105GT18GENIChomozygous118870397
51641513816415139TA13GENIChomozygous118870399
51641536116415362TG16GENIChomozygous118870401
51641574016415741CT20GENIChomozygous118870403
51641607016416071CA18GENIChomozygous118870405
51641630816416309GA21GENIChomozygous118870407
51641637316416374TC16GENIChomozygous114177242
51642042916420430CT19GENIChomozygous118870411
51642079516420796CT20GENIChomozygous118870413
51642216216422163GA15GENIChomozygous113673518
51642251016422511AG14GENIChomozygous118870415
51642253916422540CA9GENIChomozygous113673522
51642468616424687AC16GENIChomozygous113673524
51642630716426308TC18GENICheterozygous113673526
51642661116426612GA26GENIChomozygous113673528
51642667316426674CT22GENIChomozygous113673530
51642684916426850AT4GENICheterozygous126264567
51642685016426851CT5GENICheterozygous126264569
51642695516426956GA14GENIChomozygous113673534
51642759916427600GC20GENIChomozygous118870419
51642843516428436AG24GENIChomozygous113673536
51642857016428571TA14GENIChomozygous114108689
51642857116428572CA12GENICheterozygous114108690
51642857216428573TA12GENIChomozygous114108691
51642871316428714TA20GENIChomozygous118870421
51642962516429626CT20GENIChomozygous113673544
51643206616432067AG15GENIChomozygous113673550
51643234216432343GA33GENIChomozygous118870423
51643554416435545TG6GENIChomozygous122247653
51643753316437534CT6GENIChomozygous113673572
51643808916438090GA25GENIChomozygous113673576
51643827216438273AG19GENIChomozygous113673578
51643843716438438AG10GENIChomozygous113673580
51643849816438499AG25GENIChomozygous113673582
51644092616440927GC13GENIChomozygous119007353
51644194316441944GT26GENIChomozygous118870425
51644399616443997CT21GENIChomozygous113673588
51644481416444815TC13GENIChomozygous113673592
51644509416445095AC19GENIChomozygous113673594