chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	17019691	17019692	T	C	40	GENIC	homozygous	137389560
5	17020107	17020108	C	T	40	GENIC	homozygous	137389561
5	17020912	17020913	G	C	42	GENIC	homozygous	137389562
5	17021243	17021244	T		6	GENIC	heterozygous	403593008
5	17021243	17021244	T	C	6	GENIC	homozygous	403593009
5	17021369	17021370	C	T	29	GENIC	homozygous	137389564
5	17022555	17022556	A	G	35	GENIC	homozygous	154269299
5	17022555	17022556	A		35	GENIC	heterozygous	403593011
5	17022943	17022944	A	G	49	GENIC	homozygous	137389565
5	17024239	17024240	C	T	46	GENIC	homozygous	137389566
5	17026204	17026205	G	A	48	GENIC	possibly homozygous	137389567
5	17030544	17030545	G	A	48	GENIC	homozygous	137389568
5	17032211	17032212	A	T	51	GENIC	homozygous	137389570
5	17033520	17033521	G	C	45	GENIC	possibly homozygous	137389571
5	17033631	17033632	T	C	45	GENIC	homozygous	137389572
5	17033673	17033674	A	C	40	GENIC	homozygous	137389573
5	17035897	17035898	T		41	GENIC	possibly homozygous	137293168
5	17021626	17021626		TTT	35	GENIC	homozygous	137293164
5	17026682	17026698	AGAGGGCAAAGAGGGA		31	GENIC	homozygous	137293165
5	17027872	17027873	T		35	GENIC	homozygous	137293166
5	17028585	17028586	A		33	GENIC	homozygous	137293167
5	17021755	17021755		TG	18	GENIC	possibly homozygous	143174216
5	17026412	17026413	C	T	10	GENIC	possibly homozygous	143196979
5	17028997	17028998	A	C	36	GENIC	homozygous	143196980
5	17036464	17036465	G	A	42	GENIC	homozygous	137389574
5	17038190	17038191	T	C	45	GENIC	homozygous	137389575
5	17039513	17039514	A	G	50	GENIC	homozygous	137389577
5	17040446	17040447	C	T	43	GENIC	homozygous	137389578
5	17037784	17037786	TG		44	GENIC	homozygous	137293169
5	17038030	17038031	A		40	GENIC	homozygous	137293170