chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157581749157581750TA7INTERGENIChomozygous57536839
4157583728157583729CT7INTERGENIChomozygous57536877
4157584181157584182TG21INTERGENICpossibly homozygous57536887
4157585816157585817TA7INTERGENICheterozygous58511203
4157586499157586500TG22INTERGENIChomozygous57536911
4157588029157588030GA5INTERGENIChomozygous58511205
4157588815157588816TC6INTERGENICheterozygous57536941
4157588853157588854GA12INTERGENIChomozygous57536945
4157589336157589337CG13INTERGENICheterozygous57536948
4157590104157590105CCT1INTERGENIChomozygous57536956
4157590878157590879AG15INTERGENIChomozygous57536968
4157590916157590917AC13INTERGENICpossibly homozygous57536970
4157591355157591356AG2INTERGENIChomozygous57536974
4157591577157591578AC4INTERGENIChomozygous57536978
4157592104157592105CA5INTERGENICheterozygous58511209
4157592786157592787AG16INTERGENIChomozygous58511211
4157593367157593369GT--6INTERGENICheterozygous58511213
4157593379157593380GA6INTERGENICheterozygous58511215
4157595627157595628TC10INTERGENIChomozygous57537002
4157595809157595810CA4INTERGENIChomozygous58511217
4157595810157595811AT4INTERGENIChomozygous58511219
4157596001157596002GA12INTERGENIChomozygous58511221