chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	95096903	95096904	T	C	17	GENIC	homozygous	137852131
6	95097117	95097118	T	G	17	GENIC	homozygous	137852132
6	95097246	95097246		GG	10	GENIC	homozygous	137698417
6	95101149	95101150	T		17	GENIC	possibly homozygous	144749346
6	95101178	95101179	A		16	GENIC	homozygous	144749347
6	95101183	95101185	AA		16	GENIC	homozygous	144749348
6	95101870	95101871	A	G	22	GENIC	homozygous	137852134
6	95102244	95102245	A	T	27	GENIC	homozygous	137852135
6	95102634	95102634		A	26	GENIC	homozygous	137698420
6	95103516	95103517	T	C	26	GENIC	homozygous	137852137
6	95103995	95103996	G	A	18	GENIC	homozygous	137852138
6	95107188	95107189	A	G	22	GENIC	homozygous	137852139
6	95107310	95107311	A	G	27	GENIC	homozygous	137852140
6	95111880	95111881	T		16	GENIC	homozygous	144749349
6	95113817	95113818	G	C	24	GENIC	homozygous	137852142
6	95116192	95116193	A	T	25	GENIC	homozygous	137852143
6	95116972	95116973	G	T	18	GENIC	possibly homozygous	137852144
6	95118222	95118223	T		14	GENIC	homozygous	137698423
6	95118623	95118624	A	G	28	GENIC	homozygous	137852145
6	95119978	95119979	C	A	13	GENIC	homozygous	137852146
6	95120038	95120038		A	13	GENIC	homozygous	137698424
6	95120861	95120862	T	G	27	GENIC	homozygous	137852147
6	95121382	95121383	G	A	12	GENIC	homozygous	137852148
6	95122654	95122655	T	C	16	GENIC	homozygous	137852149
6	95122654	95122655	T		16	GENIC	heterozygous	403179731
6	95101149	95101150	T	A	17	GENIC	heterozygous	403179722
6	95101153	95101154	T		16	GENIC	heterozygous	403179723
6	95101153	95101154	T	A	16	GENIC	homozygous	403179724
6	95102839	95102840	C	T	27	GENIC	homozygous	144769870
6	95115909	95115910	G	C	22	GENIC	homozygous	144769872
6	95122673	95122674	C	T	21	GENIC	homozygous	137852150