chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	49950516	49950517	T	TC	36	GENIC	homozygous	55323666
6	49950558	49950559	C	T	47	GENIC	homozygous	55323668
6	49950938	49950939	G	A	37	GENIC	heterozygous	55323670
6	49950939	49950940	T	TCA	36	GENIC	heterozygous	55323672
6	49950949	49950950	T	A	36	GENIC	heterozygous	55323674
6	49950953	49950954	T	C	37	GENIC	heterozygous	55323676
6	49950955	49950957	TC	--	31	GENIC	homozygous	55323678
6	49951104	49951106	GT	--	33	GENIC	possibly homozygous	55323680
6	49951129	49951131	TG	--	24	GENIC	homozygous	55323682
6	49951172	49951176	GTGT	----	25	GENIC	heterozygous	55323684
6	49951202	49951203	A	ATG	20	GENIC	possibly homozygous	55323686
6	49951252	49951253	A	G	38	GENIC	possibly homozygous	55323688
6	49951288	49951289	A	G	28	GENIC	heterozygous	55323690
6	49951290	49951291	C	CTT	23	GENIC	heterozygous	55323692
6	49951296	49951297	C	T	33	GENIC	heterozygous	55323694
6	49951309	49951317	TGTGTGTG	--------	30	GENIC	possibly homozygous	54878470
6	49951316	49951317	G	A	31	GENIC	heterozygous	55323696
6	49951463	49951464	T	A	76	GENIC	possibly homozygous	55323698
6	49952817	49952818	C	T	52	GENIC	homozygous	55149340
6	49953038	49953039	G	T	41	GENIC	homozygous	55149341
6	49953689	49953690	T	C	52	GENIC	homozygous	54379993
6	49954160	49954161	C	T	74	GENIC	homozygous	54379995
6	49954672	49954673	T	TTGTCCAGTATG	28	GENIC	homozygous	54379997
6	49955058	49955059	T	C	39	GENIC	homozygous	54380001
6	49956371	49956372	C	A	34	GENIC	heterozygous	55323700
6	49956794	49956795	T	G	42	GENIC	homozygous	54380003