chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	30413757	30413758	G	A	24	GENIC	homozygous	47805187
17	30419389	30419390	G	GGT	4	GENIC	homozygous	47805189
17	30427002	30427003	A	C	11	GENIC	homozygous	47079388
17	30427013	30427014	G	C	12	GENIC	homozygous	47079389
17	30436402	30436403	C	CA	33	GENIC	homozygous	47079441
17	30436405	30436406	A	T	34	GENIC	homozygous	47319862
17	30436408	30436409	T	-	34	GENIC	homozygous	47079442
17	30440460	30440461	T	-	11	GENIC	heterozygous	47319866
17	30471744	30471745	C	CCT	14	GENIC	heterozygous	47805191
17	30471748	30471750	AA	--	16	GENIC	heterozygous	47805193
17	30472363	30472364	G	GT	24	GENIC	homozygous	47079501
17	30478663	30478664	C	CATAG	3	GENIC	homozygous	47805195
17	30519248	30519249	T	-	32	GENIC	homozygous	47079568
17	30519255	30519256	A	T	30	GENIC	homozygous	47079569
17	30519312	30519313	C	-	22	GENIC	homozygous	47079570
17	30519324	30519325	G	-	22	GENIC	homozygous	47079571
17	30527460	30527461	C	CA	19	GENIC	homozygous	47079608
17	30484688	30484691	ATA	---	1	GENIC	homozygous	47779724