chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4126887139126887140TG13GENIChomozygous113302597
4126887270126887271CT26GENIChomozygous113302598
4126887411126887412AT20GENIChomozygous113302599
4126887674126887675GA22GENIChomozygous119535472
4126887845126887846TC9GENIChomozygous113302600
4126888179126888180GT22GENIChomozygous113302602
4126888588126888589CT34GENIChomozygous113302603
4126888971126888972GC33GENIChomozygous113302608
4126888975126888976GA32GENIChomozygous113302609
4126888986126888987TC29GENIChomozygous113302610
4126889541126889542CA35GENIChomozygous113302612
4126890219126890220TC24GENIChomozygous113302613
4126890357126890358TG19GENIChomozygous113302616
4126891195126891196GT23GENIChomozygous113302617
4126891402126891403AG36GENIChomozygous119409574
4126892077126892078TC17GENIChomozygous113302620
4126892845126892846CT32GENIChomozygous119409575
4126892924126892925CT26GENIChomozygous119409576
4126893107126893108AG25GENIChomozygous113302622
4126893825126893826TC27GENIChomozygous113302623
4126895010126895011AG28GENIChomozygous119409577
4126895146126895147TG38GENIChomozygous119409578
4126896108126896109TC21GENIChomozygous119409579
4126897005126897006AC23GENIChomozygous119409580
4126897064126897065CT23GENIChomozygous119409581
4126897166126897167TC29GENIChomozygous119409582
4126897491126897492TC19GENIChomozygous113302624
4126898592126898593GA22GENIChomozygous119409583