chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5122863357122863358GC41GENIChomozygous113987842
5122869466122869466A4GENIChomozygous130313774
5122869417122869420CAC16GENIChomozygous130313770
5122869442122869442G10GENIChomozygous130313771
5122869448122869449T7GENIChomozygous130313772
5122869459122869460A5GENIChomozygous130313773
5122869438122869439GC10GENIChomozygous130322663
5122869749122869750A4GENIChomozygous130313775
5122883534122883535AT14GENIChomozygous113987884
5122883543122883544T14GENICheterozygous130313779
5122869752122869753A4GENIChomozygous130313776
5122869764122869764G9GENIChomozygous130313777
5122869774122869776TA14GENIChomozygous130313778
5122887109122887110CA31GENICheterozygous122381582
5122887126122887127AG32GENICheterozygous114526408
5122887209122887210AT29GENICheterozygous113987889
5122887221122887222AG30GENICheterozygous114244601
5122887224122887225CT29GENICheterozygous114244602
5122887590122887591GC35GENICheterozygous130322664
5122887606122887607GA34GENICheterozygous130322665
5122887612122887613GA32GENICheterozygous130322666
5122889086122889087GA80GENICheterozygous130322667
5122889506122889506T64GENICheterozygous130313780
5122889577122889578GC81GENICheterozygous113987901
5122890112122890113TA54GENICheterozygous130322668