chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	43485094	43485095	T	C	53	GENIC	homozygous	109707526
19	43485096	43485097	G	C	54	GENIC	homozygous	109783734
19	43485098	43485100	TA		54	GENIC	homozygous	129610576
19	43485109	43485110	C		50	GENIC	homozygous	129610577
19	43485111	43485112	G	A	50	GENIC	homozygous	110006356
19	43485119	43485120	G		49	GENIC	homozygous	129610578
19	43485125	43485125		T	51	GENIC	homozygous	129610579
19	43485128	43485129	G	T	49	GENIC	homozygous	110006358
19	43485142	43485143	T	C	50	GENIC	homozygous	109707528
19	43485146	43485147	G	A	51	GENIC	homozygous	110006361
19	43485162	43485163	G	C	52	GENIC	homozygous	109928566
19	43485168	43485169	T		51	GENIC	homozygous	129610580
19	43496653	43496653		TGCTTGCTAGG	27	GENIC	homozygous	129610591
19	43496656	43496656		G	31	GENIC	homozygous	129610592
19	43496657	43496658	A	G	36	GENIC	homozygous	124580337
19	43496659	43496659		TCTA	36	GENIC	homozygous	129610593
19	43496664	43496666	TC		41	GENIC	homozygous	129610594
19	43496667	43496667		AGC	41	GENIC	homozygous	129610595
19	43496668	43496668		AAATCCCCAAA	42	GENIC	homozygous	129610596