chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	23971196	23971197	A	G	17	GENIC	homozygous	111761477
16	23972760	23972761	C	T	42	GENIC	homozygous	111761479
16	23972780	23972781	A	G	39	GENIC	homozygous	111761481
16	23974308	23974309	T	C	21	GENIC	homozygous	111761483
16	23975214	23975215	A	G	52	GENIC	homozygous	111761485
16	23981356	23981357	T	C	69	GENIC	homozygous	111761487
16	23982519	23982520	T	C	44	GENIC	possibly homozygous	119103266
16	23983639	23983640	A	G	68	GENIC	heterozygous	119103267
16	23984145	23984146	A	T	18	GENIC	homozygous	112108700
16	23984244	23984245	C	T	31	GENIC	homozygous	112108702
16	23984248	23984249	A	G	30	GENIC	homozygous	112108704
16	23984714	23984715	G	A	37	GENIC	homozygous	119103268
16	23984768	23984769	C	T	46	GENIC	homozygous	119103269
16	23985612	23985613	T	A	10	GENIC	homozygous	119103270
16	23985729	23985730	A	G	27	GENIC	homozygous	111761489
16	23986092	23986093	G	A	27	GENIC	homozygous	111761491
16	23986200	23986201	A	T	18	GENIC	homozygous	111761493
16	23986446	23986447	A	C	27	GENIC	homozygous	111761495
16	23986641	23986642	T	C	35	GENIC	homozygous	111761497
16	23986642	23986643	A	G	35	GENIC	homozygous	111761499
16	23987178	23987179	G	A	31	GENIC	homozygous	119103271
16	23987528	23987529	A	G	50	GENIC	homozygous	111761501
16	23987929	23987930	C	T	47	GENIC	homozygous	111761503
16	23988504	23988505	G	A	41	GENIC	possibly homozygous	111761505
16	23989390	23989391	T	G	64	GENIC	homozygous	111761507
16	23990202	23990203	G	T	39	GENIC	homozygous	111761509
16	23990263	23990264	T	A	56	GENIC	homozygous	111761511
16	23990538	23990539	C	T	64	GENIC	homozygous	111761513
16	23990609	23990610	G	A	54	GENIC	homozygous	111761515
16	23990638	23990639	A	T	48	GENIC	homozygous	111761517
16	23990864	23990865	C	A	30	GENIC	homozygous	112151247
16	23990866	23990867	A	T	30	GENIC	homozygous	119103272
16	23990867	23990868	A	T	30	GENIC	homozygous	112151249
16	23990894	23990895	G	A	24	GENIC	possibly homozygous	111761519
16	23990999	23991000	G	T	19	GENIC	homozygous	111761521