chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103268595103268596GT46GENIChomozygous116832500
10103268597103268598GT46GENIChomozygous116832502
10103268607103268608GT31GENIChomozygous116832504
10103268610103268611GT30GENIChomozygous116832506
10103268612103268613AT30GENIChomozygous116832508
10103268617103268618GT30GENIChomozygous116832510
10103268621103268622CT30GENIChomozygous116832512
10103268638103268639AT39GENIChomozygous116832514
10103289548103289549GA30GENIChomozygous116713609
10103289562103289563TG31GENIChomozygous116713611
10103290209103290210CT35GENIChomozygous116713613
10103290210103290211CT35GENIChomozygous116713615
10103290919103290920TA22GENIChomozygous116713617
10103290939103290940TC25GENIChomozygous116713619
10103290950103290951GC26GENIChomozygous116713621
10103290964103290965TC31GENIChomozygous116713623
10103291083103291084TC33GENIChomozygous116713625
10103291087103291088TC34GENIChomozygous116713627
10103291105103291106GC36GENIChomozygous116713629
10103291126103291127GC36GENIChomozygous116713631
10103291134103291135TC33GENIChomozygous116713633
10103291292103291293GC21GENIChomozygous117105449
10103291295103291296TC21GENIChomozygous117105451
10103291598103291599CT53GENIChomozygous116713635
10103293123103293124AG34GENIChomozygous116713639