chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11845679	11845680	A	G	42	GENIC	homozygous	47021054
17	11846541	11846542	T	C	36	GENIC	homozygous	47021056
17	11847110	11847114	TAAC	----	3	GENIC	homozygous	47021058
17	11847119	11847120	T	A	5	GENIC	homozygous	47021060
17	11847367	11847369	TT	--	5	GENIC	homozygous	47021062
17	11847708	11847722	GTGTGTGTGTGTGT	--------------	18	GENIC	homozygous	47021065
17	11847743	11847744	T	C	14	GENIC	homozygous	47722461
17	11847745	11847746	T	C	18	GENIC	homozygous	47722463
17	11847786	11847787	C	T	21	GENIC	homozygous	47366110
17	11848614	11848620	TGTGTG	------	9	GENIC	heterozygous	47722465
17	11848616	11848620	TGTG	----	9	GENIC	heterozygous	47722467
17	11849085	11849086	C	CT	4	GENIC	homozygous	47366112
17	11849116	11849141	TTTTTTTTTTTTTTTTTTTTTTTTT	-------------------------	1	GENIC	homozygous	47722469
17	11851630	11851631	A	AT	20	GENIC	homozygous	47021069
17	11852136	11852137	T	TCTC	13	GENIC	homozygous	47021071
17	11852177	11852178	T	C	12	GENIC	possibly homozygous	47021073
17	11852212	11852213	C	CTCT	15	GENIC	homozygous	47021074
17	11852224	11852225	C	T	14	GENIC	homozygous	47722471
17	11852287	11852288	T	C	14	GENIC	possibly homozygous	47722473
17	11852426	11852427	T	TCC	10	GENIC	homozygous	47722475
17	11852427	11852428	T	TC	10	GENIC	homozygous	47722477