chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134909241949092420CT39GENIChomozygous791008047
134909454549094546GT36GENIChomozygous791008048
134909517449095175GC23GENIChomozygous791008049
134909540549095406AG27GENIChomozygous791008050
134909582549095826AC32GENIChomozygous791008051
134909638849096389GA31GENIChomozygous791008052
134909697349096974CT41GENIChomozygous791008053
134909725749097258GA23GENIChomozygous791008054
134909745749097458TC21GENICpossibly homozygous791008055
134909773249097733AG25GENIChomozygous791008056
134909813249098133CT15GENIChomozygous791008057
134909831249098313TC27GENIChomozygous791008058
134909915049099151GA35GENIChomozygous791008059
134909966849099669GC15GENIChomozygous791008060
134910029949100300CT45GENIChomozygous791008061
134910087549100876GA23GENIChomozygous791008062
134910158849101589GT22GENIChomozygous791008063
134910207849102079TC16GENIChomozygous791008064
134910254049102541CG32GENIChomozygous791008065
134910380649103807AG42GENIChomozygous791008066
134910413649104137CT36GENIChomozygous791008067
134910435649104357TC34GENIChomozygous791008068
134910500149105002AG32GENIChomozygous791008069
134910535849105359CT36GENIChomozygous791008070
134910771849107719AG34GENIChomozygous791008071
134910806349108064TC26GENIChomozygous791008072
134910817149108172AG31GENIChomozygous791008073
134910874949108750CT26GENIChomozygous791008074