chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160175313160175314AG13GENIChomozygous114160561
5160175334160175335GA20GENIChomozygous114160562
5160175639160175640CT25GENIChomozygous114160563
5160175689160175690GA24GENIChomozygous114160564
5160175712160175713CT18GENIChomozygous114160565
5160175801160175802AC32GENIChomozygous114160566
5160175943160175944TG23GENIChomozygous114160567
5160175958160175959GA22GENIChomozygous114160568
5160175975160175976AG26GENIChomozygous114160569
5160176397160176398AG20GENIChomozygous114160571
5160176809160176810AG27GENIChomozygous114160572
5160176821160176822AT25GENIChomozygous114160573
5160176836160176837AG27GENIChomozygous114160574
5160177294160177295CT13GENIChomozygous114160575
5160177640160177641GA23GENIChomozygous114160576
5160177642160177643CA22GENIChomozygous114160577
5160177896160177897TC22GENIChomozygous114160578
5160178257160178258CT20GENIChomozygous114160579
5160178894160178895GC14GENIChomozygous114160583
5160179022160179023TC6GENIChomozygous114160584
5160179232160179233AG25GENIChomozygous114160585
5160179918160179919TC16GENIChomozygous114160586