chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	41100422	41100422		TCTCCG	13	GENIC	homozygous	129249126
15	41149979	41149980	G	A	6	GENIC	heterozygous	124151193
15	41172449	41172450	T	A	16	GENIC	homozygous	112914231
15	41172462	41172462		G	13	GENIC	homozygous	129249153
15	41172464	41172464		T	13	GENIC	homozygous	129249154
15	41172487	41172487		TT	11	GENIC	homozygous	129249155
15	41172197	41172201	GTGT		4	GENIC	homozygous	130592557
15	41172496	41172497	A		12	GENIC	homozygous	129249156
15	41172501	41172502	G		12	GENIC	homozygous	129249157
15	41172511	41172512	A		10	GENIC	homozygous	129249158
15	41172540	41172540		G	5	GENIC	homozygous	129249159
15	41172559	41172559		G	5	GENIC	homozygous	129249160
15	41172574	41172576	AT		5	GENIC	homozygous	129249161
15	41172579	41172579		T	5	GENIC	homozygous	129249162
15	41172585	41172586	T		4	GENIC	homozygous	129249163
15	41172588	41172589	T		4	GENIC	homozygous	129249164
15	41172611	41172611		G	4	GENIC	homozygous	129249165
15	41172620	41172620		G	3	GENIC	homozygous	129249166
15	41149543	41149544	G	A	16	GENIC	heterozygous	119034143
15	41106025	41106027	TG		2	GENIC	homozygous	133686768
15	41172448	41172449	A	T	16	GENIC	homozygous	113294549
15	41172504	41172505	C	T	12	GENIC	homozygous	112879281
15	41180659	41180659		A	16	GENIC	homozygous	129249179