chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76569379565693796TC25GENIChomozygous144373720
76569383165693832GA24GENIChomozygous144373721
76569392265693922T7GENIChomozygous144367812
76569396465693964CTAGGT4GENIChomozygous144367813
76569417665694177TA21GENIChomozygous144373722
76569422365694228ATAAA24GENIChomozygous144367814
76569455765694558A12GENIChomozygous144367815
76569478965694790AG17GENIChomozygous144373723
76569502365695024TC10GENIChomozygous144373724
76569504165695042CT10GENIChomozygous144373725
76569520865695209AG29GENIChomozygous144373726
76569530565695306TC12GENIChomozygous144373727
76569540065695401CT13GENIChomozygous144373728
76569552565695526CG15GENIChomozygous144373729
76569578265695783TA14GENIChomozygous138108823
76569581065695811T12GENIChomozygous144367816
76569609465696095CT7GENIChomozygous144373730
76569636465696365TC17GENIChomozygous144373731
76569656465696565GA15GENIChomozygous144373732
76569662765696628CT16GENIChomozygous144373733
76569719465697195GA17GENIChomozygous144373734
76569869165698692GA19GENICpossibly homozygous144373735
76569943565699436AG8GENIChomozygous138108827
76569953265699533TC9GENICheterozygous403614861
76569953265699533T9GENIChomozygous403614862
76570007265700073CT16GENIChomozygous138108828
76570109865701110TTTTGTTTTGTT22GENIChomozygous144367817
76570133165701332GA17GENIChomozygous144373736
76570199965702000TC20GENIChomozygous138108835
76570226765702268C10GENIChomozygous144367818
76570230165702302CT7GENIChomozygous144373737
76570350565703506GC14GENIChomozygous138108840
76570510865705109GC10GENIChomozygous144373738