chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	55063533	55063534	C	T	12	GENIC	homozygous	116496494
8	55064937	55064938	G	C	26	GENIC	homozygous	116496496
8	55065061	55065062	T	A	21	GENIC	homozygous	116496498
8	55065258	55065259	T	C	21	GENIC	homozygous	116496500
8	55066664	55066665	A	G	16	GENIC	homozygous	116496504
8	55067810	55067811	T	C	25	GENIC	homozygous	116496508
8	55069371	55069372	G	A	19	GENIC	homozygous	117183327
8	55072649	55072650	A	C	12	GENIC	homozygous	116496510
8	55074870	55074871	G	A	22	GENIC	homozygous	116496512
8	55076977	55076978	T	A	29	GENIC	homozygous	116496516
8	55079827	55079828	G	T	31	GENIC	heterozygous	117183328
8	55081221	55081222	A	T	36	GENIC	homozygous	116496524
8	55081520	55081521	G	A	35	GENIC	homozygous	117183329
8	55082926	55082927	A	T	23	GENIC	homozygous	116496530
8	55084363	55084364	G	A	26	GENIC	homozygous	117183330
8	55085322	55085323	A	G	12	GENIC	homozygous	117183331
8	55085482	55085483	C	T	14	GENIC	possibly homozygous	117183332