chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	64551819	64551820	C	T	9	GENIC	homozygous	53941322
7	64551870	64551871	G	A	12	GENIC	possibly homozygous	53941323
7	64552217	64552218	C	T	13	GENIC	homozygous	53941324
7	64552577	64552578	C	T	16	GENIC	homozygous	53941325
7	64552638	64552639	C	T	15	GENIC	possibly homozygous	53941326
7	64552687	64552689	TG	--	14	GENIC	homozygous	53941327
7	64553193	64553194	C	G	17	GENIC	possibly homozygous	53941328
7	64553944	64553945	G	A	13	GENIC	homozygous	53941329
7	64553978	64553979	T	C	16	GENIC	homozygous	53941330
7	64554103	64554104	A	-	15	GENIC	possibly homozygous	53941331
7	64554221	64554222	T	C	12	GENIC	possibly homozygous	53941332
7	64554498	64554499	T	C	10	GENIC	possibly homozygous	53941333
7	64554842	64554843	G	A	19	GENIC	possibly homozygous	53941334
7	64557848	64557849	A	C	8	GENIC	homozygous	53941338
7	64557888	64557889	A	G	11	GENIC	homozygous	53941339
7	64557988	64557989	A	T	5	GENIC	homozygous	53941340
7	64558075	64558076	A	T	7	GENIC	possibly homozygous	53941341
7	64558217	64558218	C	T	18	GENIC	possibly homozygous	53941347
7	64558324	64558325	T	C	21	GENIC	possibly homozygous	53941348
7	64558470	64558471	A	G	16	GENIC	homozygous	53941349
7	64558833	64558834	G	A	16	GENIC	homozygous	53941350
7	64559107	64559108	G	GT	8	GENIC	heterozygous	53941351
7	64559957	64559958	G	-	20	GENIC	homozygous	53941352
7	64560275	64560276	C	T	19	GENIC	possibly homozygous	53941353
7	64560454	64560455	A	G	22	GENIC	heterozygous	53941354
7	64560455	64560456	G	A	23	GENIC	heterozygous	54196632
7	64560577	64560578	C	T	25	GENIC	homozygous	53941355
7	64561100	64561101	A	AT	3	GENIC	homozygous	53941356
7	64561434	64561435	G	A	4	GENIC	heterozygous	53941358
7	64562072	64562073	C	A	3	GENIC	homozygous	53941359
7	64562252	64562253	C	T	2	GENIC	homozygous	53941361