chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
156072235060722351AG27GENIChomozygous977129576
156072251560722516CT17GENIChomozygous977129577
156072300660723007TG16GENIChomozygous977129578
156072320060723201AC31GENIChomozygous977129579
156072339460723395TA35GENIChomozygous977129580
156072358960723590CT32GENIChomozygous977129581
156072404160724042TG30GENIChomozygous977129582
156072404360724044TC30GENIChomozygous977129583
156072406660724067AG31GENIChomozygous977129584
156072410360724104TC25GENIChomozygous977129585
156072418360724184TC21GENIChomozygous977129586
156072557560725576TC15GENIChomozygous977129587
156072719360727194TA33GENICheterozygous977129588
156072762960727630CT24GENIChomozygous977129589
156072763060727631CA24GENIChomozygous977129590
156073477660734777TA24GENIChomozygous977129591
156073854060738541GA25GENICpossibly homozygous977129592
156073856260738563CT25GENICpossibly homozygous977129593
156073861660738617GA30GENIChomozygous977129594
156073873060738731CT33GENIChomozygous977129595
156073893760738938GA29GENIChomozygous977129596
156073906260739063GA32GENIChomozygous977129597
156074183860741839CT30GENIChomozygous977129598
156074745360747454AG29GENIChomozygous977129599
156074838960748390CA15GENICheterozygous977129600
156074907160749072GT32GENIChomozygous977129601
156074908060749081GA33GENIChomozygous977129602
156074995560749956CA26GENIChomozygous977129603
156075067960750680AG32GENIChomozygous977129604
156075134560751346TC34GENIChomozygous977129605
156075184260751843TA26GENIChomozygous977129606
156075431260754313TC22GENIChomozygous977129607
156075599360755994AG22GENIChomozygous977129608
156076161960761620TG19GENIChomozygous977129609
156076164660761647GA13GENICpossibly homozygous977129610
156076218560762186GA17GENIChomozygous977129611
156076598760765988AG21GENIChomozygous977129612
156076648860766489GC5GENIChomozygous977129613
156076649160766492AC5GENIChomozygous977129614