chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5140539287140539288AG18GENIChomozygous114030510
5140540318140540319GA16GENIChomozygous114250950
5140542762140542763TC21GENIChomozygous114030549
5140546038140546039AG20GENIChomozygous114030570
5140547462140547463TC27GENIChomozygous114030573
5140547667140547668TC30GENICpossibly homozygous114030575
5140548269140548270AT17GENIChomozygous114250954
5140550194140550195CT21GENIChomozygous114030579
5140550286140550287GA30GENIChomozygous114030580
5140550662140550663GA25GENIChomozygous114030581
5140551268140551269GA19GENIChomozygous114030582
5140551305140551306CT14GENIChomozygous114030583
5140551702140551703TC25GENIChomozygous114030584
5140552214140552215TC27GENIChomozygous114030585
5140552323140552324CT24GENIChomozygous114030586
5140552440140552441GA28GENIChomozygous114030587
5140552805140552806AG30GENIChomozygous114030588
5140552939140552940CA18GENIChomozygous114030589
5140553482140553483GA25GENIChomozygous114030590
5140553546140553547GA28GENIChomozygous114030591
5140554537140554538CA25GENIChomozygous114030592
5140554558140554559CT30GENIChomozygous114030593
5140554842140554843GA24GENIChomozygous114250956
5140555106140555107GC20GENIChomozygous118845988
5140555164140555165GA18GENIChomozygous114030594
5140556079140556080CA38GENIChomozygous114030595
5140556095140556096GC41GENIChomozygous114030596
5140556600140556601AG29GENIChomozygous114030597