chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5129511891129511892CT57GENIChomozygous143959125
5129512603129512604CT50GENIChomozygous143959126
5129512840129512841AT64GENIChomozygous143959127
5129515800129515801CG45GENIChomozygous143959128
5129516963129516964AC55GENIChomozygous143959129
5129519412129519413AG57GENIChomozygous143959130
5129519983129519984GA49GENIChomozygous143959131
5129520124129520125CT47GENIChomozygous143959132
5129520490129520491CT45GENIChomozygous137620186
5129523786129523787GA46GENIChomozygous143959133
5129523992129523993CT65GENIChomozygous143959134
5129525414129525415TC57GENIChomozygous143959135
5129526168129526169CT26GENIChomozygous146140766
5129526277129526278GC49GENIChomozygous143959136
5129527969129527970CT69GENIChomozygous143959137
5129528501129528502TG47GENIChomozygous137620190
5129528533129528534CT53GENIChomozygous143959138
5129531345129531346GA33GENICpossibly homozygous143959139
5129532275129532276GA48GENIChomozygous143959140
5129518141129518257CTACAGACTGTATTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCTTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC37GENIChomozygous143943613
5129518794129518798ATAT52GENIChomozygous143943614
5129522946129522946GA44GENIChomozygous143943615
5129528331129528335TAAA38GENIChomozygous143943616
5129528917129528920CAG35GENIChomozygous143943617
5129526118129526118CTTTTCTTTTC12GENICheterozygous146771172
5129526037129526038GC16GENICheterozygous403600041
5129526037129526038G16GENICheterozygous403600040