chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15747159757471598TG18GENIChomozygous108111589
15747190257471903CT22GENIChomozygous108111590
15747208257472083TG17GENIChomozygous108111591
15747246757472468AT32GENIChomozygous108111592
15747392257473923TC16GENIChomozygous108111593
15747417257474173TC35GENIChomozygous108111594
15747463557474636CT34GENICpossibly homozygous108111595
15747558757475588GT24GENIChomozygous108111596
15747589757475898GC23GENIChomozygous108111597
15747652557476526AG20GENIChomozygous108111601
15747900857479009GC25GENIChomozygous108111605
15747901357479014CT27GENIChomozygous108111606
15748119457481195TC24GENIChomozygous108111613
15748126157481262TC37GENIChomozygous108111614
15748149657481497TC29GENIChomozygous108111615
15748227557482276AG30GENIChomozygous108111616
15748240957482410CT41GENIChomozygous108111617
15748277957482780GA43GENIChomozygous108111618
15748304457483045GA38GENIChomozygous108111621
15748310057483101AT43GENIChomozygous108111622
15748311557483116GA37GENIChomozygous108111623
15748522457485225GA17GENIChomozygous108111630
15748590657485907TC26GENIChomozygous108111631
15748609257486093TC34GENIChomozygous108111632
15748650057486501TC32GENIChomozygous108111633
15748714657487147AG24GENIChomozygous108111634
15748818657488187CA29GENIChomozygous108111635
15748891757488918AG32GENIChomozygous108111636
15748938457489385TC17GENIChomozygous108111637
15748952957489530GA13GENIChomozygous108111638
15749033657490337TC18GENIChomozygous108111639
15749077457490775TC16GENIChomozygous108111641