chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	200037846	200037847	C	G	31	GENIC	homozygous	108502948
1	200082407	200082408	T	C	16	GENIC	homozygous	108502952
1	200089184	200089185	G	T	28	GENIC	homozygous	109363250
1	200039464	200039465	A	G	15	GENIC	homozygous	109363247
1	200082384	200082385	G	A	21	GENIC	heterozygous	109363248
1	200082397	200082398	T	C	17	GENIC	homozygous	109363249
1	200089615	200089616	G	A	33	GENIC	homozygous	109363251
1	200091092	200091093	C	T	21	GENIC	homozygous	108502954
1	200092336	200092337	T	C	25	GENIC	homozygous	108502958
1	200094805	200094806	C	A	37	GENIC	homozygous	109363252
1	200094844	200094845	G	T	32	GENIC	homozygous	108765870
1	200096126	200096127	A	G	19	GENIC	homozygous	109363253
1	200096203	200096204	C	A	29	GENIC	homozygous	109363254
1	200096223	200096224	A	C	34	GENIC	homozygous	109363255
1	200099876	200099877	T	C	38	GENIC	homozygous	109363256
1	200102337	200102338	G	C	43	GENIC	homozygous	108502966
1	200102768	200102769	A	G	24	GENIC	homozygous	108502968
1	200103259	200103260	A	G	17	GENIC	homozygous	108502970
1	200103287	200103288	A	G	18	GENIC	homozygous	108502972
1	200103734	200103735	C	A	22	GENIC	homozygous	108502974
1	200103867	200103868	T	G	24	GENIC	homozygous	109363257
1	200103883	200103884	G	A	25	GENIC	homozygous	109363258
1	200105292	200105293	G	A	29	GENIC	homozygous	108502976
1	200105691	200105692	T	C	39	GENIC	homozygous	108502978
1	200107695	200107696	T	C	34	GENIC	homozygous	108502980
1	200110097	200110098	A	G	20	GENIC	homozygous	109363259
1	200111928	200111929	T	C	29	GENIC	homozygous	108502988
1	200112449	200112450	A	G	37	GENIC	homozygous	108502990
1	200112480	200112481	A	G	38	GENIC	homozygous	109363260
1	200112530	200112531	T	G	33	GENIC	homozygous	109363261
1	200112829	200112830	A	G	39	GENIC	homozygous	108502992
1	200115478	200115479	T	C	30	GENIC	homozygous	108502998