chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	85099395	85099396	T	C	21	GENIC	homozygous	116665152
10	85099419	85099420	C	G	27	GENIC	homozygous	116814894
10	85100955	85100956	G	A	32	GENIC	homozygous	116665154
10	85101303	85101304	G	A	40	GENIC	homozygous	116665156
10	85103151	85103152	G	A	26	GENIC	homozygous	116665158
10	85103513	85103514	T	A	31	GENIC	homozygous	116665160
10	85103665	85103666	T	C	10	GENIC	homozygous	116665162
10	85104696	85104697	T	A	29	GENIC	homozygous	116665164
10	85105730	85105731	C	G	20	GENIC	homozygous	116665166
10	85106691	85106692	T	C	3	GENIC	homozygous	117104982
10	85108057	85108058	T	G	32	GENIC	homozygous	116665168
10	85110565	85110566	G	A	21	GENIC	homozygous	116665170
10	85111742	85111743	C	T	33	GENIC	homozygous	116665172
10	85114723	85114724	A	T	21	GENIC	possibly homozygous	116814896
10	85115416	85115417	G	A	24	GENIC	homozygous	116665174
10	85115454	85115455	A	T	31	GENIC	homozygous	116665176
10	85116123	85116124	G	A	26	GENIC	homozygous	116665178
10	85118112	85118113	G	T	27	GENIC	homozygous	116665182
10	85121441	85121442	C	G	26	GENIC	homozygous	116665184
10	85122786	85122787	G	A	24	GENIC	homozygous	116665186
10	85123568	85123569	A	G	14	GENIC	homozygous	116665188