chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109095809090958091AAG21GENIChomozygous51538783
109095810390958104CG23GENIChomozygous51738333
109095887390958874AG40GENIChomozygous51738335
109095954790959548CG42GENIChomozygous51738337
109095954890959549CT44GENIChomozygous51738339
109095958890959589AG34GENIChomozygous51738341
109095967390959683TGGGGACGTT----------23GENIChomozygous51738343
109095972790959728AG19GENIChomozygous51738346
109096167690961677AC36GENIChomozygous51738348
109096226190962262AG35GENIChomozygous51738350
109096300590963006CG42GENIChomozygous51738352
109096337490963375GC32GENIChomozygous51738354
109096401190964018GAAAAGA-------13GENIChomozygous51538784
109096401290964016AAAA----13GENIChomozygous51538785
109096403390964034GGT15GENICheterozygous51738356
109096403790964038T-16GENICheterozygous51538786
109096404590964046TTGTGC13GENICpossibly homozygous51738358
109096404590964046TC15GENICheterozygous51928353
109096406290964063TG20GENICpossibly homozygous51538787
109096431890964319CT49GENIChomozygous51738360
109096446390964464TTAA30GENIChomozygous51738362
109096451890964525GGGGTTC-------21GENIChomozygous51738364
109096495590964956CA37GENIChomozygous51928356
109096501490965016TG--7GENICheterozygous51738366
109096556890965569CT28GENIChomozygous51928359
109096557890965579CCA24GENIChomozygous51928363
109096561690965617TTAC15GENICpossibly homozygous51738372
109096592290965923TA50GENIChomozygous51928366
109096610190966102TC27GENICpossibly homozygous51928369
109096625590966256CT35GENIChomozygous51928372
109096643190966432CCTT9GENIChomozygous51738376
109096649290966493C-29GENIChomozygous51928375
109096692790966936TTTTTTTTT---------6GENICheterozygous51928378
109096699790966998A-29GENIChomozygous51738378
109096795190967952TG40GENIChomozygous51538789
109096807790968078AG42GENIChomozygous51738381