chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11695569016955691GGTAAGTCCTCTAGT23GENIChomozygous737916029
11695673716956738AG15GENIChomozygous619177765
11695702216957026GTGG----15GENIChomozygous737916030
11695797016957971GGGGCTTCACTGACGTCGATGACGCTCTGGCATTGGTTC19GENICpossibly homozygous737916031
11695802116958022TG20GENIChomozygous619177766
11695821616958217CT23GENIChomozygous619177767
11695837516958376AG22GENIChomozygous619177768
11695869316958694TC21GENIChomozygous619177769
11695888216958883TA13GENIChomozygous619177770
11695922716959228TTTTTTTTTTTTTTTTGTTTTTTGTTTTTTG14GENICpossibly homozygous737916032
11695942016959421AT24GENIChomozygous619177771