chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89352872	89352873	A	T	10	GENIC	homozygous	116675323
10	89353216	89353217	T	C	21	GENIC	homozygous	116819883
10	89353244	89353245	T	A	17	GENIC	homozygous	117087448
10	89353340	89353341	G	A	31	GENIC	homozygous	116902366
10	89353659	89353660	A	C	26	GENIC	homozygous	116902368
10	89353790	89353791	A	C	29	GENIC	homozygous	116902370
10	89354061	89354062	G	T	31	GENIC	homozygous	117105222
10	89354188	89354189	T	A	36	GENIC	homozygous	117087450
10	89354209	89354210	G	T	41	GENIC	homozygous	117087452
10	89354474	89354475	C	T	11	GENIC	homozygous	116902372
10	89354515	89354516	T	G	13	GENIC	homozygous	116675329
10	89354529	89354530	T	C	12	GENIC	homozygous	116902374
10	89354885	89354886	G	A	21	GENIC	homozygous	116675331
10	89355190	89355191	T	C	32	GENIC	possibly homozygous	117087454
10	89355242	89355243	C	T	24	GENIC	homozygous	116902384
10	89355278	89355279	G	A	31	GENIC	homozygous	116902386
10	89355334	89355335	A	G	41	GENIC	homozygous	116902388
10	89356084	89356085	C	G	38	GENIC	homozygous	116675339
10	89356128	89356129	G	A	32	GENIC	homozygous	116902392