chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174410894444108945AAG11GENIChomozygous47113741
174410907244109073CT24GENIChomozygous47113742
174411160244111603TC26GENIChomozygous47113744
174411218344112184TA31GENIChomozygous47113746
174411258944112593AAAC----29GENIChomozygous47113747
174411298844112989GGCCCCCGTCA27GENIChomozygous47113748
174411343744113438GT23GENIChomozygous47113750
174411358544113586CT28GENIChomozygous47113752
174411359144113592CCTTTTTTT18GENICheterozygous47709028
174411359244113594TT--18GENICheterozygous47113753
174411530144115303AT--24GENIChomozygous47709030
174411530344115304TTCTCCA22GENIChomozygous47709032
174411568344115685TT--3GENICheterozygous47709034
174411610144116117TTTTTTTTTTTTTTTT----------------5GENICheterozygous47856244
174411651144116512GC28GENIChomozygous47113762
174411729744117298CG38GENIChomozygous47113763
174411743344117434TG29GENIChomozygous47113765
174411752244117523GGA26GENIChomozygous47113766
174411797644117980AAAC----22GENIChomozygous47113768
174411839044118404CACACACACACACG--------------10GENIChomozygous47113769
174411855044118551CT34GENIChomozygous47113771
174411871144118712AC23GENIChomozygous47113773
174411902944119041CCCAGATGCCAT------------26GENIChomozygous47113774
174411926144119262AG34GENIChomozygous47113776
174411948144119482TC25GENIChomozygous47113777
174411979244119793TA30GENIChomozygous47113779
174411990844119909CCA28GENIChomozygous47113781
174412042644120429ATG---31GENIChomozygous47113782
174412098844120989GGA23GENICpossibly homozygous47113784
174412098844120989GGAA23GENICheterozygous47739436
174412135744121358CT24GENIChomozygous47113785