chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	49622776	49622777	G	A	34	GENIC	homozygous	116489075
8	49622796	49622797	C	T	29	GENIC	homozygous	116489077
8	49622806	49622807	G	A	27	GENIC	homozygous	116489079
8	49622846	49622847	G	A	26	GENIC	homozygous	116489081
8	49622873	49622874	C	T	23	GENIC	homozygous	116489083
8	49622892	49622893	C	T	28	GENIC	homozygous	116489085
8	49624949	49624950	A	G	33	GENIC	homozygous	116489097
8	49624950	49624951	T	C	35	GENIC	homozygous	116489099
8	49625027	49625028	T	G	38	GENIC	homozygous	116489101
8	49625052	49625053	A	G	41	GENIC	homozygous	116489103
8	49625087	49625088	C	T	39	GENIC	homozygous	116489105
8	49626541	49626542	A	G	34	GENIC	homozygous	116489109
8	49626857	49626858	G	A	26	GENIC	homozygous	116489111
8	49627445	49627446	C	G	41	GENIC	homozygous	116489113
8	49627446	49627447	C	T	40	GENIC	homozygous	116489115
8	49627768	49627769	A	G	30	GENIC	homozygous	116489117
8	49627779	49627780	T	C	32	GENIC	homozygous	116489119
8	49629917	49629918	C	T	43	GENIC	homozygous	116489121
8	49630276	49630277	G	T	37	GENIC	homozygous	116489123
8	49632843	49632844	G	T	26	GENIC	homozygous	116489125
8	49634297	49634298	A	C	40	GENIC	homozygous	116489127
8	49636369	49636370	C	T	29	GENIC	homozygous	116489131
8	49637578	49637579	G	A	33	GENIC	homozygous	116489133
8	49639210	49639211	T	C	31	GENIC	homozygous	116489135
8	49639882	49639883	T	G	28	GENIC	homozygous	116489137
8	49640562	49640563	C	T	41	GENIC	homozygous	116489139
8	49640730	49640731	T	C	27	GENIC	homozygous	116489141
8	49640863	49640864	C	T	32	GENIC	homozygous	116489143
8	49641262	49641263	A	G	27	GENIC	homozygous	116489145
8	49641886	49641887	T	C	39	GENIC	homozygous	116489147
8	49647419	49647420	G	A	43	GENIC	homozygous	116489149
8	49647956	49647957	C	A	26	GENIC	homozygous	116489151
8	49648103	49648104	A	G	35	GENIC	homozygous	116489153
8	49649238	49649239	C	T	30	GENIC	homozygous	116489155
8	49649250	49649251	T	C	29	GENIC	homozygous	116489157
8	49649826	49649827	T	G	30	GENIC	homozygous	116489159