chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149902465149902466GA10GENIChomozygous112882630
4149902573149902574GA12GENIChomozygous112882631
4149902953149902954CT21GENIChomozygous112882632
4149903003149903004CT16GENIChomozygous112882633
4149903121149903122TG24GENICpossibly homozygous112882634
4149903640149903641AG22GENIChomozygous112882635
4149903765149903766AG24GENIChomozygous112882636
4149903790149903791GA7GENIChomozygous112882637
4149904033149904034AG19GENIChomozygous112882638
4149904070149904071AT10GENIChomozygous112882639
4149904072149904073GA8GENIChomozygous112882640
4149904145149904146AT11GENIChomozygous112882641
4149904186149904187TG14GENIChomozygous112882642
4149904194149904195TC17GENIChomozygous112882643
4149904239149904240AG9GENIChomozygous112882644
4149904246149904247AG7GENIChomozygous112882645
4149904272149904273TC10GENIChomozygous112882646
4149904410149904411TC20GENIChomozygous112882647
4149904505149904506TA6GENICheterozygous112882648
4149904513149904514TA8GENIChomozygous112882649
4149904595149904596GT23GENIChomozygous112882650
4149904741149904742GT27GENIChomozygous112882651
4149905111149905112TC6GENIChomozygous112882656
4149905116149905117TC8GENIChomozygous112882657
4149905120149905121GC12GENIChomozygous112882658
4149905151149905152CT4GENIChomozygous112882659
4149905236149905237TC21GENIChomozygous112882661
4149905281149905282GA11GENIChomozygous112882662
4149905311149905312GA17GENIChomozygous112882663
4149905746149905747GA28GENIChomozygous112882664
4149906284149906285AG11GENIChomozygous112882665
4149906458149906459CA6GENIChomozygous126081989
4149906459149906460TA8GENICheterozygous119281940
4149906672149906673CA15GENIChomozygous112882666
4149907558149907559AG19GENIChomozygous112882667
4149908206149908207CT30GENIChomozygous112882668
4149908629149908630AG20GENIChomozygous112882669
4149908689149908690AG17GENIChomozygous112882670
4149909787149909788GT13GENIChomozygous112882671