chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112710311627103117GT23GENIChomozygous116033023
112710426527104266TA28GENIChomozygous116033025
112710429527104296TC22GENIChomozygous115799053
112710701327107014TC18GENIChomozygous115799061
112710704827107049CG19GENIChomozygous115799063
112710979427109795CT14GENIChomozygous115956487
112710990027109901TC16GENIChomozygous115799071
112711316427113165TC34GENIChomozygous115799077
112711404727114048CT26GENIChomozygous115799081
112711420727114208TC23GENIChomozygous115799083
112711481027114811TG26GENIChomozygous115799085
112711483127114832AC31GENIChomozygous115799087
112711488827114889GC35GENIChomozygous115956491
112711493627114937CG31GENIChomozygous115956492
112711497927114980GA33GENIChomozygous115799089
112711500627115007AT33GENIChomozygous116242419
112710782227107823GC17GENIChomozygous116242414
112710816527108166GA17GENIChomozygous116242415
112710932027109321AT26GENIChomozygous116242416
112711380727113808CT28GENIChomozygous116242418
112711695427116955AG31GENIChomozygous115799101
112711812727118128CG23GENIChomozygous115799105
112711812927118130AT22GENIChomozygous115799107
112711821827118219CT19GENIChomozygous115956493
112712086027120861TC23GENIChomozygous115799111
112712156427121565TC22GENIChomozygous115799113
112712169327121694GA23GENIChomozygous115799115
112712175927121760GA30GENICpossibly homozygous115799117
112712183227121833AT27GENIChomozygous115799119
112712309727123098AG19GENIChomozygous115799121
112712311627123117GA24GENIChomozygous115799123
112712352927123530CT23GENIChomozygous115799125
112712543727125438CT29GENIChomozygous115799129
112712547127125472CA28GENIChomozygous115799131
112712831827128319TC41GENIChomozygous115799135
112712924227129243AG38GENIChomozygous115799141
112712951327129514CT33GENIChomozygous116242420