chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10257816	10257817	C	A	47	GENIC	possibly homozygous	140403496
19	10258399	10258399		GA	52	GENIC	homozygous	140376310
19	10258749	10258749		AAGGCTGGAGACTGGG	39	GENIC	homozygous	140376311
19	10258904	10258905	T	C	47	GENIC	homozygous	140403497
19	10259800	10259801	T	G	22	GENIC	homozygous	140403499
19	10260470	10260471	T		45	GENIC	homozygous	140376313
19	10263412	10263413	T	C	50	GENIC	homozygous	140403508
19	10259932	10259933	T	G	41	GENIC	homozygous	140403500
19	10260104	10260105	A	G	35	GENIC	homozygous	140403501
19	10261348	10261349	A	G	37	GENIC	homozygous	140403504
19	10262386	10262387	A	G	32	GENIC	homozygous	140403506
19	10262762	10262763	C	T	53	GENIC	homozygous	140403507
19	10261802	10261803	A		8	GENIC	heterozygous	148417188
19	10259271	10259272	A	G	48	GENIC	homozygous	147377967
19	10260555	10260556	C	T	16	GENIC	homozygous	147377968
19	10259428	10259428		TCTGTGTGTGTG	25	GENIC	heterozygous	147376324
19	10262528	10262529	T		54	GENIC	homozygous	147376325
19	10261802	10261803	A	G	8	GENIC	homozygous	403442117
19	10261806	10261807	A	G	6	GENIC	homozygous	404100477
19	10263942	10263943	A	G	46	GENIC	homozygous	140403509
19	10263978	10263979	T	C	51	GENIC	homozygous	140403510
19	10264105	10264106	C	T	59	GENIC	homozygous	147377969