chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76569379565693796TC47GENIChomozygous144373720
76569383165693832GA40GENIChomozygous144373721
76569392265693922T28GENIChomozygous144367812
76569396465693964CTAGGT30GENIChomozygous144367813
76569417665694177TA42GENIChomozygous144373722
76569422365694228ATAAA42GENIChomozygous144367814
76569455765694558A45GENIChomozygous144367815
76569478965694790AG48GENIChomozygous144373723
76569502365695024TC50GENIChomozygous144373724
76569504165695042CT53GENIChomozygous144373725
76569520865695209AG46GENIChomozygous144373726
76569530565695306TC45GENIChomozygous144373727
76569540065695401CT48GENIChomozygous144373728
76569552565695526CG44GENIChomozygous144373729
76569578265695783TA42GENICpossibly homozygous138108823
76569581065695811T43GENICpossibly homozygous144367816
76569609465696095CT19GENICpossibly homozygous144373730
76569636465696365TC53GENIChomozygous144373731
76569656465696565GA40GENIChomozygous144373732
76569662765696628CT34GENIChomozygous144373733
76569719465697195GA42GENIChomozygous144373734
76569869165698692GA67GENIChomozygous144373735
76569943565699436AG32GENIChomozygous138108827
76569953265699533TC25GENICheterozygous403614861
76569953265699533T25GENIChomozygous403614862
76570007265700073CT40GENIChomozygous138108828
76570109865701110TTTTGTTTTGTT49GENIChomozygous144367817
76570133165701332GA55GENIChomozygous144373736
76570199965702000TC53GENIChomozygous138108835
76570226765702268C30GENIChomozygous144367818
76570230165702302CT36GENIChomozygous144373737
76570350565703506GC49GENIChomozygous138108840
76570510865705109GC44GENIChomozygous144373738