chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149902573149902574GA4GENIChomozygous112882631
4149902953149902954CT20GENIChomozygous112882632
4149903003149903004CT17GENIChomozygous112882633
4149903640149903641AG15GENIChomozygous112882635
4149903765149903766AG14GENIChomozygous112882636
4149904070149904071AT10GENIChomozygous112882639
4149904072149904073GA8GENIChomozygous112882640
4149904145149904146AT5GENIChomozygous112882641
4149904186149904187TG14GENIChomozygous112882642
4149904194149904195TC14GENIChomozygous112882643
4149904239149904240AG10GENIChomozygous112882644
4149904246149904247AG6GENIChomozygous112882645
4149904272149904273TC9GENIChomozygous112882646
4149904410149904411TC15GENIChomozygous112882647
4149904505149904506TA5GENIChomozygous112882648
4149904513149904514TA8GENIChomozygous112882649
4149904595149904596GT15GENIChomozygous112882650
4149904741149904742GT14GENIChomozygous112882651
4149905111149905112TC8GENIChomozygous112882656
4149905116149905117TC7GENIChomozygous112882657
4149905120149905121GC9GENIChomozygous112882658
4149905236149905237TC11GENIChomozygous112882661
4149905281149905282GA21GENIChomozygous112882662
4149905311149905312GA16GENIChomozygous112882663
4149905746149905747GA15GENIChomozygous112882664
4149906284149906285AG11GENIChomozygous112882665
4149906459149906460TA9GENIChomozygous119281940
4149906672149906673CA13GENIChomozygous112882666
4149907558149907559AG15GENIChomozygous112882667
4149908206149908207CT12GENIChomozygous112882668
4149908629149908630AG6GENIChomozygous112882669
4149908689149908690AG9GENIChomozygous112882670
4149909787149909788GT13GENIChomozygous112882671