chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5129511891129511892CT19GENIChomozygous143959125
5129512603129512604CT11GENIChomozygous143959126
5129512840129512841AT13GENIChomozygous143959127
5129515800129515801CG20GENIChomozygous143959128
5129516963129516964AC20GENIChomozygous143959129
5129519412129519413AG12GENIChomozygous143959130
5129519983129519984GA20GENIChomozygous143959131
5129520124129520125CT27GENIChomozygous143959132
5129520490129520491CT11GENIChomozygous137620186
5129523786129523787GA17GENIChomozygous143959133
5129523992129523993CT10GENIChomozygous143959134
5129525414129525415TC15GENIChomozygous143959135
5129526277129526278GC10GENIChomozygous143959136
5129527969129527970CT25GENIChomozygous143959137
5129528501129528502TG19GENIChomozygous137620190
5129528533129528534CT18GENIChomozygous143959138
5129531345129531346GA10GENIChomozygous143959139
5129532275129532276GA8GENIChomozygous143959140
5129528331129528335TAAA9GENIChomozygous143943616
5129518141129518257CTACAGACTGTATTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCTTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC15GENIChomozygous143943613
5129518794129518798ATAT20GENIChomozygous143943614
5129522946129522946GA16GENIChomozygous143943615
5129528917129528920CAG5GENIChomozygous143943617