chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	55063117	55063118	A	G	18	GENIC	homozygous	116496492
8	55063533	55063534	C	T	18	GENIC	homozygous	116496494
8	55063960	55063961	T	C	29	GENIC	homozygous	116822968
8	55064937	55064938	G	C	17	GENIC	homozygous	116496496
8	55065061	55065062	T	A	19	GENIC	homozygous	116496498
8	55065258	55065259	T	C	28	GENIC	homozygous	116496500
8	55065400	55065401	A	G	38	GENIC	heterozygous	116496502
8	55066664	55066665	A	G	19	GENIC	homozygous	116496504
8	55067267	55067268	C	T	8	GENIC	homozygous	116496506
8	55067810	55067811	T	C	18	GENIC	possibly homozygous	116496508
8	55072649	55072650	A	C	16	GENIC	homozygous	116496510
8	55074870	55074871	G	A	23	GENIC	homozygous	116496512
8	55075836	55075837	C	G	19	GENIC	homozygous	116496514
8	55076977	55076978	T	A	19	GENIC	homozygous	116496516
8	55079618	55079619	C	T	27	GENIC	heterozygous	116496518
8	55079620	55079621	C	T	26	GENIC	heterozygous	116496520
8	55079648	55079649	C	T	21	GENIC	possibly homozygous	116496522
8	55081221	55081222	A	T	26	GENIC	homozygous	116496524
8	55081510	55081511	A	C	26	GENIC	heterozygous	116496526
8	55081916	55081917	G	A	9	GENIC	homozygous	116496528
8	55082926	55082927	A	T	12	GENIC	heterozygous	116496530
8	55083065	55083066	G	A	17	GENIC	homozygous	116496532