chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	41801055	41801056	G	A	16	GENIC	homozygous	111048972
17	41801228	41801229	T	C	30	GENIC	homozygous	111048974
17	41801899	41801900	G	A	35	GENIC	homozygous	111048976
17	41802420	41802421	G	A	22	GENIC	homozygous	111048978
17	41802895	41802896	T	C	23	GENIC	homozygous	111048980
17	41803064	41803065	G	A	19	GENIC	homozygous	111048982
17	41803331	41803332	A	G	30	GENIC	homozygous	111048984
17	41803723	41803724	A	G	19	GENIC	homozygous	111048986
17	41804579	41804580	C	A	18	GENIC	possibly homozygous	111048988
17	41804691	41804692	A	T	17	GENIC	homozygous	111048990
17	41805049	41805050	A	G	23	GENIC	homozygous	111048992
17	41805653	41805654	G	A	30	GENIC	homozygous	111048994
17	41805760	41805761	T	C	19	GENIC	homozygous	111048996
17	41806052	41806053	G	T	17	GENIC	homozygous	111048998
17	41807132	41807133	C	T	11	GENIC	homozygous	111049000
17	41807849	41807850	T	C	23	GENIC	homozygous	111049002
17	41808996	41808997	A	G	17	GENIC	homozygous	111049004
17	41809399	41809400	C	G	26	GENIC	homozygous	111049006
17	41809606	41809607	C	T	21	GENIC	homozygous	111049008
17	41809607	41809608	T	A	21	GENIC	homozygous	111049010
17	41811273	41811274	T	C	17	GENIC	homozygous	111049012
17	41811480	41811481	G	A	25	GENIC	homozygous	111049014
17	41811519	41811520	T	G	28	GENIC	homozygous	111049016
17	41811800	41811801	T	C	19	GENIC	homozygous	111049018
17	41814826	41814827	G		15	GENIC	heterozygous	132507567
17	41815347	41815348	A	C	19	GENIC	homozygous	111049022
17	41815395	41815396	G	A	20	GENIC	homozygous	111049024
17	41804028	41804028		A	14	GENIC	homozygous	129450027
17	41808858	41808863	GACTC		22	GENIC	homozygous	129450028
17	41812766	41812766		T	18	GENIC	possibly homozygous	129450029
17	41813614	41813615	G	A	3	GENIC	homozygous	134072742