chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	5219340	5219341	C	T	38	GENIC	homozygous	114166505
5	5220538	5220539	G	C	47	GENIC	homozygous	113631204
5	5220563	5220564	C	T	45	GENIC	homozygous	113631205
5	5220682	5220683	G	A	55	GENIC	homozygous	113631206
5	5220693	5220694	T	C	55	GENIC	homozygous	113631207
5	5221417	5221418	T	C	6	GENIC	homozygous	114166507
5	5221489	5221490	T	C	16	GENIC	homozygous	114385712
5	5225964	5225965	T	G	59	GENIC	homozygous	113631208
5	5227420	5227421	G	A	18	GENIC	homozygous	113631209
5	5281498	5281499	G	A	26	GENIC	homozygous	113631210
5	5283282	5283283	C	T	51	GENIC	homozygous	113631211
5	5285421	5285422	C	T	42	GENIC	homozygous	114166509
5	5285521	5285522	A	G	34	GENIC	homozygous	113631212
5	5286103	5286104	C	G	35	GENIC	homozygous	114166511
5	5286433	5286434	G	A	26	GENIC	homozygous	113631214
5	5287632	5287633	A	G	47	GENIC	homozygous	113631215
5	5288941	5288942	C	G	30	GENIC	homozygous	113631216
5	5290562	5290563	C	G	62	GENIC	homozygous	113631217
5	5290961	5290962	C	T	31	GENIC	homozygous	113631218
5	5291353	5291354	G	A	48	GENIC	homozygous	113631219
5	5292183	5292184	A	G	53	GENIC	homozygous	113631220
5	5292602	5292603	G	A	43	GENIC	possibly homozygous	113631221
5	5293221	5293222	T	G	44	GENIC	possibly homozygous	113631222
5	5294042	5294043	C	T	71	GENIC	homozygous	114166513
5	5294251	5294252	C	T	56	GENIC	possibly homozygous	113631223
5	5294544	5294545	C	T	48	GENIC	homozygous	114166514
5	5294709	5294710	G	T	36	GENIC	possibly homozygous	114166516
5	5295562	5295563	G	A	51	GENIC	homozygous	114166518
5	5295929	5295930	A	G	51	GENIC	homozygous	114166519
5	5296190	5296191	C	A	48	GENIC	possibly homozygous	113631224