chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	76388003	76388003		TA	54	GENIC	homozygous	129475824
17	76388751	76388752	A	G	41	GENIC	homozygous	111095127
17	76388771	76388772	T	C	40	GENIC	homozygous	111095129
17	76390168	76390168		C	45	GENIC	homozygous	129475825
17	76393095	76393096	T	C	51	GENIC	homozygous	111095135
17	76393324	76393325	A	G	56	GENIC	homozygous	111095139
17	76393939	76393940	G	T	51	GENIC	homozygous	111095141
17	76396161	76396161		AG	52	GENIC	homozygous	129475827
17	76397807	76397808	A	G	54	GENIC	homozygous	111095147
17	76398645	76398690	GGAGAGGACTCTGGGGTTAAGGACACTTGCTGTTCATCGGGGCTA		15	GENIC	homozygous	129475829
17	76389072	76389073	T	C	24	GENIC	homozygous	131538118
17	76398084	76398085	A	C	12	GENIC	homozygous	111213316
17	76392801	76392803	AG		44	GENIC	possibly homozygous	131533509
17	76401736	76401737	A	G	45	GENIC	homozygous	111095151
17	76402111	76402112	A	G	44	GENIC	homozygous	111095153
17	76403393	76403393		T	54	GENIC	homozygous	131533510
17	76406122	76406123	T	C	49	GENIC	homozygous	111095157
17	76406326	76406327	T	C	45	GENIC	homozygous	111095159
17	76406394	76406395	A	G	40	GENIC	homozygous	111095161
17	76409142	76409143	G	A	47	GENIC	homozygous	111095163
17	76410090	76410091	A	C	50	GENIC	homozygous	111095166
17	76401011	76401012	C	T	28	GENIC	homozygous	111600791
17	76406897	76406898	A	T	46	GENIC	homozygous	111366176
17	76408304	76408305	G	C	51	GENIC	homozygous	111560112