chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117217357772173578CT12GENICheterozygous51070335
117219917772199178A-4GENICheterozygous50992432
117222642372226424T-8GENICheterozygous51167198
117223061372230732AAATAAAAAGTTATTGTGGAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAGGAGCAAGGCCCTAGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAATA-----------------------------------------------------------------------------------------------------------------------26GENICheterozygous51167220
117226009472260095GC2GENIChomozygous50825274
117226009572260096GA1GENIChomozygous50825276
117226010572260106GT1GENIChomozygous50825278
117226014672260147AT3GENIChomozygous50825282
117226014772260148AC3GENIChomozygous50825284
117226254272262543TTG4GENIChomozygous50825333
117226255672262557C-5GENICheterozygous51167234
117226673172266732A-18GENIChomozygous50825384
117227495772274958TA2GENIChomozygous50825557
117227572572275726T-2GENICheterozygous51070685
117227661172276612AG17GENICpossibly homozygous50825581
117228047372280474A-13GENICpossibly homozygous50825631
117228188572281886GA13GENICheterozygous51070755
117230765772307658AG11GENICheterozygous50825889
117231290872312909AC28GENICheterozygous51202492
117231846572318466TTGTGAG3GENIChomozygous51167237
117233704372337044AG2GENIChomozygous50826135
117237814472378145GGCACACACACACACACACACACA1GENIChomozygous51188530