chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	31961989	31961990	G	A	10	GENIC	homozygous	50932125
12	31962110	31962111	C	CCA	7	GENIC	homozygous	50442226
12	31962151	31962152	G	A	7	GENIC	homozygous	50932128
12	31962766	31962767	A	G	11	GENIC	homozygous	50442232
12	31963234	31963235	G	A	9	GENIC	homozygous	50932131
12	31963798	31963799	C	CCCGA	5	GENIC	homozygous	50442236
12	31965328	31965329	C	T	8	GENIC	homozygous	50932134
12	31965949	31965950	C	T	14	GENIC	homozygous	50442246
12	31966253	31966254	T	C	14	GENIC	homozygous	50932136
12	31966322	31966323	G	GGTGTGTGTGTGTGT	5	GENIC	heterozygous	50609711
12	31966328	31966329	T	TGTGTGTGTGTGTGTGTGTGC	5	GENIC	heterozygous	50932139
12	31966394	31966395	G	GTTTTGGGTTTGTTTTTT	5	GENIC	homozygous	50932142
12	31966494	31966495	A	G	3	GENIC	homozygous	50442250
12	31966523	31966524	A	C	4	GENIC	homozygous	50591516
12	31966524	31966525	C	A	4	GENIC	homozygous	50591517
12	31966550	31966553	CCA	---	2	GENIC	homozygous	50932145
12	31966966	31966967	G	A	5	GENIC	homozygous	50932148
12	31967103	31967107	AACA	----	7	GENIC	homozygous	50932151
12	31967119	31967120	G	T	8	GENIC	homozygous	50932154
12	31967153	31967154	A	G	8	GENIC	homozygous	50932157
12	31967197	31967198	C	T	6	GENIC	homozygous	50932160
12	31967225	31967226	A	G	7	GENIC	homozygous	50932163
12	31967230	31967231	T	C	8	GENIC	homozygous	50932166
12	31967305	31967306	T	C	8	GENIC	homozygous	50442264
12	31967330	31967331	A	G	6	GENIC	homozygous	50442266
12	31967459	31967460	G	A	8	GENIC	homozygous	50932169
12	31967881	31967882	T	G	4	GENIC	homozygous	50442268
12	31967951	31967952	A	G	8	GENIC	homozygous	50442270
12	31968259	31968260	A	C	3	GENIC	homozygous	50174766
12	31968853	31968854	T	TA	2	GENIC	homozygous	50312734
12	31969608	31969609	C	CA	4	GENIC	heterozygous	50558362
12	31969609	31969610	A	-	4	GENIC	heterozygous	50174769