chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	26785677	26785678	C	T	31	GENIC	homozygous	111010973
17	26785978	26785979	A	G	40	GENIC	homozygous	111010975
17	26786718	26786719	A	G	29	GENIC	homozygous	111010977
17	26788249	26788250	T	G	26	GENIC	homozygous	111010979
17	26787866	26787867	A	G	10	GENIC	possibly homozygous	111398875
17	26788634	26788635	C	T	21	GENIC	homozygous	111010981
17	26789508	26789509	C	T	27	GENIC	homozygous	111010983
17	26789736	26789737	C	T	24	GENIC	homozygous	111398876
17	26789738	26789739	A	G	24	GENIC	homozygous	111237439
17	26789759	26789760	A	G	21	GENIC	homozygous	111183239
17	26789834	26789835	A	G	30	GENIC	homozygous	111010985
17	26789868	26789869	G	A	24	GENIC	homozygous	111010987
17	26790059	26790060	A	G	30	GENIC	homozygous	111010989
17	26790192	26790193	T	A	30	GENIC	homozygous	111010991
17	26790568	26790569	A	G	29	GENIC	homozygous	111398877
17	26791490	26791491	A	C	27	GENIC	homozygous	111010993
17	26791513	26791514	G	C	27	GENIC	homozygous	111010995
17	26791965	26791966	C	T	33	GENIC	possibly homozygous	111010997
17	26792036	26792037	A	G	29	GENIC	homozygous	111010999
17	26792364	26792365	G	A	50	GENIC	homozygous	111011001
17	26792972	26792973	C	T	23	GENIC	homozygous	111011003
17	26793767	26793768	C	A	30	GENIC	homozygous	111011005
17	26793775	26793776	G	A	32	GENIC	homozygous	111011007
17	26795280	26795281	A	G	29	GENIC	homozygous	111011009
17	26795442	26795443	C	T	29	GENIC	possibly homozygous	111011012
17	26795699	26795700	A	G	15	GENIC	homozygous	111398878
17	26795702	26795703	A	T	15	GENIC	homozygous	111398879