chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160175313160175314AG29GENIChomozygous114160561
5160175334160175335GA30GENIChomozygous114160562
5160175580160175581CT16GENIChomozygous114259312
5160175639160175640CT26GENIChomozygous114160563
5160175689160175690GA30GENIChomozygous114160564
5160175712160175713CT33GENIChomozygous114160565
5160175801160175802AC31GENIChomozygous114160566
5160175943160175944TG25GENIChomozygous114160567
5160175975160175976AG21GENIChomozygous114160569
5160176018160176019TC16GENIChomozygous114160570
5160176397160176398AG19GENIChomozygous114160571
5160176425160176426AT23GENIChomozygous114259314
5160176663160176664AG24GENIChomozygous114259316
5160176809160176810AG20GENIChomozygous114160572
5160176821160176822AT20GENIChomozygous114160573
5160176836160176837AG22GENIChomozygous114160574
5160177294160177295CT8GENIChomozygous114160575
5160177374160177375TC27GENIChomozygous114259318
5160177640160177641GA22GENIChomozygous114160576
5160177642160177643CA21GENIChomozygous114160577
5160177896160177897TC28GENIChomozygous114160578
5160178257160178258CT26GENIChomozygous114160579
5160178581160178582TC13GENICpossibly homozygous114160580
5160178601160178602CG10GENICpossibly homozygous114160581
5160178745160178746AG17GENICheterozygous114160582
5160178894160178895GC17GENIChomozygous114160583
5160179022160179023TC16GENIChomozygous114160584
5160179232160179233AG18GENIChomozygous114160585
5160179918160179919TC15GENIChomozygous114160586