chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4699171	4699172	T	TAGACAA	17	GENIC	homozygous	50004803
12	4699187	4699188	G	C	21	GENIC	homozygous	50004807
12	4699441	4699442	A	G	13	GENIC	homozygous	50004815
12	4699552	4699553	G	A	13	GENIC	homozygous	50004817
12	4699689	4699690	C	T	15	GENIC	homozygous	50394995
12	4699883	4699884	G	A	14	GENIC	homozygous	50004819
12	4701193	4701194	A	T	7	GENIC	homozygous	50004823
12	4701219	4701220	G	A	7	GENIC	homozygous	50004825
12	4701298	4701299	C	T	8	GENIC	homozygous	50004827
12	4701409	4701410	G	A	12	GENIC	homozygous	50004829
12	4702416	4702417	C	T	12	GENIC	homozygous	50004831
12	4702676	4702677	G	A	7	GENIC	homozygous	50004833
12	4704018	4704019	T	C	9	GENIC	homozygous	50394997
12	4704033	4704034	T	C	9	GENIC	homozygous	50394999
12	4704134	4704135	C	T	15	GENIC	homozygous	50395001
12	4704283	4704284	T	C	9	GENIC	homozygous	50395003
12	4704684	4704685	T	C	7	GENIC	homozygous	50395005
12	4705806	4705807	C	T	12	GENIC	homozygous	50395007
12	4706949	4706950	A	G	17	GENIC	homozygous	50004849
12	4708031	4708032	C	T	7	GENIC	homozygous	50395009