chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	41100422	41100422		TCTCCG	44	GENIC	homozygous	129249126
15	41101117	41101118	G	C	2	GENIC	homozygous	118915019
15	41172462	41172462		G	28	GENIC	homozygous	129249153
15	41172464	41172464		T	30	GENIC	homozygous	129249154
15	41172487	41172487		TT	33	GENIC	homozygous	129249155
15	41172496	41172497	A		36	GENIC	homozygous	129249156
15	41172501	41172502	G		35	GENIC	homozygous	129249157
15	41172511	41172512	A		36	GENIC	homozygous	129249158
15	41172540	41172540		G	33	GENIC	homozygous	129249159
15	41172559	41172559		G	22	GENIC	homozygous	129249160
15	41172574	41172576	AT		20	GENIC	homozygous	129249161
15	41172579	41172579		T	20	GENIC	homozygous	129249162
15	41172585	41172586	T		19	GENIC	homozygous	129249163
15	41172588	41172589	T		18	GENIC	homozygous	129249164
15	41172611	41172611		G	15	GENIC	homozygous	129249165
15	41172620	41172620		G	11	GENIC	homozygous	129249166
15	41123618	41123727	CTAACTATGGATCAGTATTAACTAACTAACTATGGATCAGTATTAACTAACTATGGATCAGTATTAACTAACTATGGATCAGTGTTAACTAACTATGGATCAGTATTAG		35	GENIC	heterozygous	130440668
15	41134498	41134499	T		27	GENIC	heterozygous	130440669
15	41172448	41172449	A	T	29	GENIC	homozygous	113294549
15	41172449	41172450	T	A	28	GENIC	homozygous	112914231
15	41149882	41149883	A	C	12	GENIC	heterozygous	130448779
15	41172504	41172505	C	T	35	GENIC	homozygous	112879281
15	41180659	41180659		A	45	GENIC	homozygous	129249179