chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145377793145377794CG18GENIChomozygous112870837
4145377958145377959CT25GENIChomozygous112870838
4145378139145378140GC17GENIChomozygous112870839
4145380277145380278AG8GENIChomozygous112870841
4145380893145380894GA28GENIChomozygous112870842
4145381300145381301AG24GENIChomozygous112870843
4145381344145381345GA27GENIChomozygous112870844
4145382075145382076TC10GENIChomozygous112870845
4145382782145382782CACACT8GENIChomozygous128087979
4145379202145379207TTGTC11GENIChomozygous128087975
4145382526145382532TACACA13GENIChomozygous128087976
4145382588145382590AT14GENIChomozygous128087977
4145382703145382705CA6GENIChomozygous128087978
4145381839145381840CT15GENIChomozygous128136025
4145382822145382832CTCACACACT13GENIChomozygous128087980
4145383020145383032CACTCACACACA16GENIChomozygous128087981
4145383063145383063CA16GENICpossibly homozygous128087982
4145384778145384779A13GENICheterozygous131363346
4145384927145384927A24GENIChomozygous128087983
4145385061145385062GA13GENIChomozygous112870846
4145385904145385905CT18GENIChomozygous112870848
4145386018145386022ACAC18GENIChomozygous128087984
4145386110145386111GA16GENIChomozygous112870849
4145386529145386529CAAA12GENIChomozygous128087985
4145386860145386861AC21GENIChomozygous112870851
4145387394145387395TA23GENIChomozygous113178975
4145387719145387720AG21GENIChomozygous112870852
4145388150145388151CT13GENIChomozygous112870855