chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211206491211206492AG41GENIChomozygous108523144
1211206769211206769A23GENICpossibly homozygous127479490
1211207312211207313GC56GENIChomozygous109448535
1211207575211207576TA67GENIChomozygous108523146
1211208010211208011GA42GENIChomozygous108523147
1211216139211216140TC49GENIChomozygous108523171
1211211682211211683CT39GENIChomozygous109448536
1211213156211213157AG56GENIChomozygous108523162
1211213288211213289AG56GENIChomozygous109448537
1211214667211214668GT54GENIChomozygous108523166
1211215409211215410GA52GENICpossibly homozygous108523169
1211211205211211205T54GENIChomozygous131582554
1211212616211212618TG59GENIChomozygous131582555
1211213512211213512CATACTGCTCTTTTTATGTAAGTTCACGGTACACTGAAAGATCGGGTTCCATCACAGATGGTCATGAGCCACCATGTGGTTG21GENIChomozygous131582556
1211214169211214175TTGTTG43GENIChomozygous131582557
1211219571211219571T32GENICheterozygous131582558
1211220653211220654AG60GENIChomozygous109448538
1211224654211224655CA55GENICpossibly homozygous109448539
1211225925211225926CT57GENIChomozygous109448540
1211235329211235330GT68GENIChomozygous108523220
1211237783211237784AG34GENIChomozygous109448542
1211239132211239133CG50GENIChomozygous108523240