chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	88318250	88318251	T	C	29	GENIC	homozygous	116901269
10	88318336	88318337	C	T	21	GENIC	homozygous	116901271
10	88318833	88318834	C	T	17	GENIC	homozygous	116901273
10	88318876	88318877	G	A	11	GENIC	homozygous	116901275
10	88318994	88318995	G	A	16	GENIC	homozygous	116901277
10	88319055	88319056	G	C	15	GENIC	homozygous	116901279
10	88319084	88319085	T	C	15	GENIC	homozygous	116901281
10	88319121	88319122	C	T	9	GENIC	homozygous	117020348
10	88319796	88319797	G	A	15	GENIC	homozygous	116901283
10	88319993	88319994	A	G	21	GENIC	homozygous	116901285
10	88320419	88320420	C	T	21	GENIC	homozygous	116901287
10	88320588	88320589	G	A	16	GENIC	homozygous	116901289
10	88320629	88320630	T	A	11	GENIC	homozygous	116901291
10	88320800	88320801	C	G	18	GENIC	possibly homozygous	117068338
10	88321108	88321109	A	G	23	GENIC	homozygous	116901293
10	88321188	88321189	A	G	29	GENIC	homozygous	116901295
10	88321285	88321286	G	C	24	GENIC	homozygous	116901297
10	88321368	88321369	G	A	22	GENIC	homozygous	116901299
10	88321402	88321403	A	T	22	GENIC	homozygous	116901301
10	88321430	88321431	G	A	25	GENIC	homozygous	116901303
10	88321846	88321847	G	A	11	GENIC	homozygous	116901305
10	88321880	88321881	T	G	7	GENIC	homozygous	116901307
10	88321884	88321885	T	G	7	GENIC	homozygous	116901309
10	88322131	88322132	T	C	7	GENIC	homozygous	116818815
10	88322228	88322229	A	T	20	GENIC	homozygous	116901311
10	88322506	88322507	G	A	10	GENIC	homozygous	116901313
10	88322597	88322598	A	T	17	GENIC	homozygous	116901315
10	88323651	88323652	G	C	26	GENIC	homozygous	116901317
10	88323695	88323696	G	T	23	GENIC	homozygous	116901319
10	88323790	88323791	G	A	14	GENIC	homozygous	116901321
10	88324462	88324463	A	G	12	GENIC	homozygous	116901323
10	88324551	88324552	T	G	8	GENIC	homozygous	116901325
10	88324752	88324753	A	G	13	GENIC	homozygous	116818817
10	88324790	88324791	G	A	11	GENIC	homozygous	116901327