chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	171627084	171627085	T	C	19	GENIC	homozygous	119188432
5	171629071	171629072	G	A	12	GENIC	homozygous	119188433
5	171630150	171630151	C	T	6	GENIC	homozygous	119188434
5	171632750	171632751	C	T	14	GENIC	homozygous	119188435
5	171632994	171632995	G	T	24	GENIC	homozygous	119188436
5	171633225	171633226	G	A	20	GENIC	homozygous	119188437
5	171634742	171634743	T	C	14	GENIC	homozygous	119188438
5	171636574	171636575	C	T	13	GENIC	homozygous	119188439
5	171636757	171636758	G	A	22	GENIC	homozygous	119188440
5	171637799	171637800	C	G	22	GENIC	possibly homozygous	119188441
5	171638251	171638252	T	C	15	GENIC	homozygous	119188442
5	171638580	171638581	A	G	27	GENIC	homozygous	119188443
5	171639603	171639604	T	C	14	GENIC	homozygous	114292521
5	171640187	171640188	T	C	12	GENIC	homozygous	114292527
5	171640374	171640375	C	T	11	GENIC	homozygous	119188444
5	171640914	171640915	A	G	12	GENIC	homozygous	119188445
5	171641989	171641990	G	A	23	GENIC	homozygous	119188446
5	171644687	171644688	A	G	15	GENIC	homozygous	114292539
5	171645031	171645032	C	T	14	GENIC	homozygous	114292541
5	171645094	171645095	C	G	5	GENIC	homozygous	114292543
5	171645296	171645297	A	G	18	GENIC	homozygous	114292545
5	171647447	171647448	A	G	23	GENIC	homozygous	119188447
5	171647525	171647526	T	C	23	GENIC	homozygous	119188448