chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	50792561	50792563	CT	--	3	GENIC	homozygous	49187883
15	50814215	50814216	A	AG	3	GENIC	homozygous	48306058
15	50854503	50854505	GT	--	5	GENIC	heterozygous	49149185
15	50886081	50886082	C	-	11	GENIC	homozygous	48306079
15	50886092	50886094	AC	--	11	GENIC	homozygous	48306080
15	50886102	50886103	G	GC	12	GENIC	homozygous	48306081
15	50888871	50888873	GT	--	8	GENIC	heterozygous	49052486
15	50889071	50889072	G	GA	27	GENIC	homozygous	48306087
15	50889789	50889790	C	CTTTTTT	10	GENIC	heterozygous	49052487
15	50903019	50903020	G	GT	15	GENIC	heterozygous	48306106
15	50917163	50917164	T	G	13	GENIC	homozygous	48306115
15	50917179	50917180	T	G	12	GENIC	homozygous	48306117
15	50918801	50918803	CA	--	12	GENIC	heterozygous	48601712
15	50920815	50920817	CT	--	5	GENIC	heterozygous	49149186
15	50922442	50922443	T	-	9	GENIC	heterozygous	49149187
15	50922493	50922494	T	C	19	GENIC	homozygous	48306129
15	50922497	50922498	C	T	20	GENIC	homozygous	48306130
15	50922498	50922499	A	T	20	GENIC	homozygous	48306131
15	50928432	50928433	G	T	28	GENIC	homozygous	48306138
15	50928438	50928439	A	C	24	GENIC	homozygous	48306139