chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	104059231	104059232	T	A	11	GENIC	homozygous	54940192
6	104064479	104064480	C	CA	39	GENIC	homozygous	54608272
6	104069756	104069757	G	T	8	GENIC	possibly homozygous	54608295
6	104088402	104088403	G	A	19	GENIC	possibly homozygous	54608373
6	104091199	104091200	A	C	33	GENIC	homozygous	54608381
6	104102311	104102312	A	ACATGTCTTCTCTTTAGC	31	GENIC	homozygous	54940193
6	104109776	104109777	A	AGT	13	GENIC	heterozygous	54608468
6	104116479	104116480	C	CCTCCTCCTCCT	23	GENIC	homozygous	54608489
6	104116481	104116482	C	T	27	GENIC	heterozygous	54608490
6	104116484	104116485	C	T	29	GENIC	heterozygous	54608491
6	104118425	104118426	C	G	24	GENIC	homozygous	54940194
6	104137322	104137323	T	TCA	16	GENIC	homozygous	54608540
6	104137421	104137428	AGACCAC	-------	11	GENIC	homozygous	54608546
6	104143345	104143349	CACA	----	6	GENIC	heterozygous	54608558
6	104143347	104143349	CA	--	6	GENIC	heterozygous	54940195
6	104145152	104145153	A	C	18	GENIC	heterozygous	54608567
6	104159626	104159627	C	G	15	GENIC	homozygous	54608599
6	104159628	104159629	C	G	11	GENIC	homozygous	54608600
6	104159630	104159631	C	G	10	GENIC	homozygous	54608601
6	104159641	104159642	C	G	13	GENIC	homozygous	54608602
6	104159644	104159645	T	A	14	GENIC	homozygous	54608603
6	104159645	104159646	T	G	15	GENIC	homozygous	54608604
6	104159649	104159650	C	G	16	GENIC	homozygous	54608605
6	104164979	104164981	AG	--	13	GENIC	homozygous	54608622
6	104164980	104164981	G	GAT	14	GENIC	heterozygous	54608623
6	104165534	104165535	G	C	33	GENIC	homozygous	54608626
6	104175878	104175879	C	CCT	12	GENIC	heterozygous	54940196
6	104179666	104179669	GGG	---	9	GENIC	heterozygous	54608651
6	104179667	104179669	GG	--	9	GENIC	possibly homozygous	54608652
6	104110115	104110116	A	T	1	GENIC	homozygous	55046741
6	104175878	104175879	C	CCTCT	12	GENIC	heterozygous	55046742
6	104116475	104116480	TTCTC	-----	21	GENIC	heterozygous	54843057
6	104161108	104161109	C	CT	4	GENIC	heterozygous	54843061