chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46277857562778575ATCA54GENIChomozygous136887504
46277914062779141AG69GENIChomozygous137064969
46278246362782464GT63GENIChomozygous137064970
46278246462782465AC62GENIChomozygous137064971
46278340562783406TA64GENIChomozygous137064972
46278348062783481TC59GENIChomozygous137064973
46278509862785099GA49GENIChomozygous137064974
46278546662785467AG30GENIChomozygous137064975
46278606962786070CG50GENIChomozygous137064976
46278748862787489GA66GENIChomozygous137064977
46279017862790288TCAAAAATATTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGAACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC65GENIChomozygous136887505
46279149762791498TC75GENIChomozygous137064978
46279176862791769TC56GENIChomozygous137064979
46279366562793666AG58GENIChomozygous137064980
46279374062793741TC65GENIChomozygous137064981
46279411662794117CT51GENIChomozygous137064982
46279435362794354TC63GENIChomozygous137064983
46279491062794911GA60GENIChomozygous137064984
46279548762795488GA34GENIChomozygous137064985
46279560862795608AC19GENIChomozygous136887506
46279667162796672AT7GENIChomozygous403581349
46279667162796672A7GENICheterozygous403581350
46279666962796670AT7GENIChomozygous403581347
46279666962796670A7GENICheterozygous403581348
46279667362796674AT7GENIChomozygous403581351
46279667562796676AT7GENIChomozygous137064986
46279667762796678AT7GENIChomozygous137064987
46279667962796680AT7GENIChomozygous137064988
46279668162796682AT7GENIChomozygous137064989
46279668362796684AT7GENIChomozygous137064990
46279740562797406TC66GENIChomozygous137064991
46279758762797588TC42GENIChomozygous137064992
46279760362797603CATTTTCATATTCTTATC41GENIChomozygous136887507
46279828662798287AC59GENIChomozygous137064993
46279850762798508TC59GENIChomozygous137064994