chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59594124	59594125	C	A	11	GENIC	homozygous	53272590
8	59594533	59594534	C	T	25	GENIC	homozygous	53272591
8	59595061	59595062	T	C	15	GENIC	homozygous	52664068
8	59595243	59595244	T	C	11	GENIC	homozygous	53272592
8	59596324	59596325	G	A	19	GENIC	homozygous	53272593
8	59596559	59596560	T	C	18	GENIC	homozygous	53272594
8	59596999	59597058	TATTATAGGAAATAGATAATTTTACTTTTTCCTCTCCAGCTTGGATCAATTTTATTTAC	-----------------------------------------------------------	5	GENIC	homozygous	53388679
8	59597237	59597238	C	T	19	GENIC	homozygous	53272595
8	59597256	59597257	G	GTGTAA	19	GENIC	homozygous	53272597
8	59597365	59597366	C	A	10	GENIC	homozygous	53272598
8	59597430	59597431	C	CAAA	7	GENIC	homozygous	52983291
8	59597687	59597688	G	A	7	GENIC	homozygous	53272601
8	59598668	59598669	A	-	18	GENIC	homozygous	52983292
8	59599276	59599277	C	T	20	GENIC	homozygous	53272602
8	59599291	59599292	C	T	18	GENIC	homozygous	53272603
8	59602402	59602403	T	TA	13	GENIC	homozygous	53272604
8	59602616	59602617	T	A	24	GENIC	homozygous	53272605
8	59603281	59603282	A	G	13	GENIC	homozygous	52664084
8	59603988	59603989	T	C	9	GENIC	homozygous	52664086
8	59604055	59604056	G	A	10	GENIC	homozygous	53272606
8	59604494	59604495	C	A	12	GENIC	homozygous	53272607
8	59604655	59604656	C	T	14	GENIC	homozygous	53272608
8	59604957	59604958	C	CACCCTTGCCGCTTCACTTCTTGAGAACGCGCGCGCACGCGCGCTCTCACCAA	19	GENIC	heterozygous	53570150
8	59604976	59604977	G	GAAAAAAAA	10	GENIC	heterozygous	53388680
8	59604977	59604978	A	-	10	GENIC	heterozygous	52664088
8	59605092	59605093	T	-	12	GENIC	homozygous	52664090
8	59605328	59605329	C	A	10	GENIC	homozygous	53272609
8	59605333	59605334	A	AC	10	GENIC	homozygous	53122433
8	59606600	59606608	AAACAAAC	--------	19	GENIC	homozygous	53902567
8	59606721	59606722	G	T	12	GENIC	homozygous	53272610