chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	24110604	24110605	A	G	31	GENIC	homozygous	142695369
19	24111022	24111023	G	A	50	GENIC	homozygous	142695370
19	24111403	24111404	C	T	63	GENIC	homozygous	142695371
19	24112033	24112033		CCTGAAACTCAGAGTTCTC	43	GENIC	homozygous	140383320
19	24112080	24112080		CT	38	GENIC	homozygous	140383321
19	24112193	24112194	T	C	51	GENIC	homozygous	140431750
19	24112787	24112788	C	T	40	GENIC	homozygous	142695372
19	24116483	24116483		T	40	GENIC	homozygous	142678715
19	24116245	24116246	T	A	38	GENIC	homozygous	142695375
19	24116246	24116247	T	C	39	GENIC	homozygous	142695376
19	24117238	24117239	A	G	49	GENIC	homozygous	142695377
19	24117827	24117828	T	G	54	GENIC	homozygous	140431754
19	24116539	24116540	T	G	50	GENIC	homozygous	148390259
19	24117909	24117910	G	T	48	GENIC	possibly homozygous	148390260
19	24116963	24117086	GGCCTTGAACTTCTTTTTGGTTCTTTTTTTTTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGTGCTTCTTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC		10	GENIC	heterozygous	140928418