chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42778672927786729GTGCTTGCTAGGCAA14GENIChomozygous128017626
42778673327786733TCTA12GENIChomozygous128017627
42778673527786735ACT10GENIChomozygous128017628
42778673627786737GA10GENIChomozygous122014859
42782196627821967T11GENICheterozygous132395910
42782631927826319TCTTGGTCAGGCCCATGTTG11GENIChomozygous128017629
42783159127831591A6GENIChomozygous128017630
42783258727832587C1GENIChomozygous128017631
42783542127835421T2GENIChomozygous128017633
42783543027835431T2GENIChomozygous128017634
42783543827835439TG4GENIChomozygous112565510
42783544327835443T4GENIChomozygous128017635
42783545627835457G5GENIChomozygous128017636
42783545827835459A5GENIChomozygous128017637
42786188927861890GT19GENICheterozygous113256102
42786191127861912GT20GENICheterozygous113256103
42788534027885341AG7GENIChomozygous126086698
42792523627925238TA12GENIChomozygous128017642
42792523927925239TCA12GENIChomozygous128017643
42792529127925292AC18GENIChomozygous112565518
42792530427925304C18GENIChomozygous128017644
42792533327925334C18GENIChomozygous128017645
42792533727925337A17GENIChomozygous128017646
42792534227925343C17GENIChomozygous128017647
42792535427925356GT15GENIChomozygous128017648
42792536127925361T14GENIChomozygous128017649