chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	103638426	103638427	T	C	22	GENIC	homozygous	52779345
8	103640624	103640625	A	G	22	GENIC	homozygous	52779346
8	103641451	103641452	C	T	17	GENIC	homozygous	52779347
8	103641768	103641769	A	C	21	GENIC	homozygous	52779348
8	103641982	103641983	A	G	11	GENIC	homozygous	52779349
8	103642155	103642156	A	G	22	GENIC	homozygous	52779350
8	103642175	103642176	C	G	22	GENIC	homozygous	52779351
8	103642324	103642325	T	C	22	GENIC	homozygous	52779352
8	103642643	103642644	A	G	14	GENIC	homozygous	52779353
8	103646000	103646001	C	A	14	GENIC	homozygous	52779364
8	103646177	103646178	T	C	19	GENIC	homozygous	52779365
8	103647563	103647564	C	T	18	GENIC	homozygous	52779372
8	103647844	103647845	T	C	14	GENIC	homozygous	52779373
8	103649108	103649109	C	CA	15	GENIC	heterozygous	52779375
8	103649126	103649127	T	C	19	GENIC	homozygous	52779376
8	103649925	103649926	A	AT	9	GENIC	homozygous	52779377
8	103651575	103651576	C	T	11	GENIC	homozygous	52779378
8	103654987	103654988	G	A	19	GENIC	homozygous	52779380
8	103655221	103655222	T	-	15	GENIC	homozygous	52779381
8	103655267	103655268	A	-	20	GENIC	homozygous	52779382
8	103655268	103655269	A	T	19	GENIC	homozygous	53406405
8	103656939	103656940	A	T	19	GENIC	homozygous	52779384
8	103656948	103656949	T	-	20	GENIC	homozygous	52779385
8	103657792	103657793	A	-	17	GENIC	homozygous	52779389
8	103657805	103657806	T	A	16	GENIC	homozygous	52779390
8	103658007	103658008	G	A	16	GENIC	homozygous	52779391
8	103658104	103658105	C	T	20	GENIC	homozygous	52779392
8	103658507	103658508	C	T	19	GENIC	homozygous	53367103
8	103658508	103658509	T	G	19	GENIC	homozygous	52779393
8	103658663	103658664	G	A	22	GENIC	homozygous	52779394
8	103661198	103661199	T	C	10	GENIC	homozygous	52779399
8	103661366	103661367	G	A	14	GENIC	homozygous	52779400
8	103661830	103661831	T	C	13	GENIC	homozygous	52779401
8	103662156	103662157	A	G	18	GENIC	homozygous	52779402