chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212589681212589682TC42GENICpossibly homozygous108988522
1212589772212589773CT61GENIChomozygous108988523
1212589960212589961TC55GENIChomozygous108988524
1212589999212590000TC63GENIChomozygous108988526
1212591315212591316AT37GENIChomozygous120591659
1212591388212591389GA32GENIChomozygous120591662
1212591669212591670CT44GENIChomozygous108988535
1212591999212592000CT26GENIChomozygous120591664
1212592258212592259TC29GENIChomozygous108988540
1212593662212593663TG36GENIChomozygous108988554
1212597126212597127AG29GENIChomozygous108988591
1212598085212598086GA33GENIChomozygous120591666
1212598279212598280CT24GENIChomozygous120591668
1212601182212601183AG36GENIChomozygous108988606
1212601986212601987CT53GENIChomozygous120591670
1212602821212602822TG27GENIChomozygous108988609