chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	23854639	23854640	A	G	26	GENIC	homozygous	110998105
17	23854695	23854696	C	T	34	GENIC	homozygous	110998107
17	23854696	23854697	T	G	33	GENIC	homozygous	110998109
17	23854885	23854886	T	C	33	GENIC	homozygous	110998111
17	23855104	23855105	T	C	40	GENIC	homozygous	110998113
17	23855373	23855374	G	C	26	GENIC	homozygous	110998116
17	23855558	23855559	T	C	26	GENIC	homozygous	110998118
17	23855680	23855681	A	G	25	GENIC	homozygous	110998120
17	23855752	23855753	A	G	33	GENIC	homozygous	110998122
17	23855895	23855896	A	G	37	GENIC	homozygous	110998124
17	23856116	23856117	G	A	35	GENIC	homozygous	110998126
17	23856129	23856130	C	T	42	GENIC	homozygous	110998128
17	23856291	23856292	T	A	20	GENIC	homozygous	111340204
17	23856583	23856584	A	T	25	GENIC	homozygous	110998130
17	23856733	23856734	A	G	28	GENIC	homozygous	110998132
17	23856894	23856895	C	A	34	GENIC	homozygous	110998134
17	23857283	23857284	C	T	28	GENIC	homozygous	110998136
17	23857630	23857631	G	A	30	GENIC	homozygous	110998138
17	23857640	23857641	T	C	28	GENIC	homozygous	110998140
17	23859194	23859195	C	T	24	GENIC	homozygous	110998142
17	23859515	23859516	T	C	18	GENIC	homozygous	110998144
17	23859671	23859672	A	G	24	GENIC	homozygous	110998146
17	23860001	23860002	C	T	36	GENIC	homozygous	111180437
17	23860267	23860268	A	G	30	GENIC	homozygous	110998148