chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	43999299	43999300	C	G	12	GENIC	homozygous	142238391
10	44000123	44000123		ATGG	10	GENIC	homozygous	142201344
10	44001506	44001507	T	C	20	GENIC	homozygous	142238392
10	44001522	44001523	A	C	21	GENIC	homozygous	142238393
10	44002333	44002334	A	G	14	GENIC	homozygous	142238394
10	44003982	44003982		ACTC	16	GENIC	homozygous	138681681
10	44004171	44004173	CA		11	GENIC	homozygous	142201345
10	44004172	44004173	A		11	GENIC	homozygous	403285131
10	44004150	44004151	A	G	13	GENIC	homozygous	154634493
10	44004158	44004159	A	G	14	GENIC	homozygous	154634494
10	44004172	44004173	A	G	11	GENIC	heterozygous	154634495
10	44004150	44004151	A		13	GENIC	heterozygous	403285129
10	44004158	44004159	A		14	GENIC	heterozygous	403285130
10	44004319	44004320	C	T	20	GENIC	homozygous	142238395
10	44004883	44004886	GGT		7	GENIC	homozygous	138681684
10	44006454	44006455	A		17	GENIC	homozygous	142201346
10	44007041	44007042	A	G	6	GENIC	homozygous	142238396
10	44009888	44009889	C	T	11	GENIC	homozygous	142238397
10	44011206	44011207	A	C	14	GENIC	homozygous	142238398
10	44013439	44013439		TAGCTAGC	10	GENIC	homozygous	138681686
10	44008950	44008951	C	T	13	GENIC	homozygous	138782153