chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	1915758	1915758		A	28	GENIC	possibly homozygous	139817051
16	1915759	1915760	C	A	29	GENIC	homozygous	139853348
16	1915768	1915769	C	A	28	GENIC	homozygous	139853349
16	1916082	1916083	A	G	18	GENIC	homozygous	139853350
16	1916121	1916122	G	A	19	GENIC	homozygous	139853351
16	1916347	1916348	G	A	23	GENIC	homozygous	139853352
16	1916543	1916544	G	A	15	GENIC	homozygous	139853353
16	1916795	1916796	T	C	26	GENIC	homozygous	139853354
16	1916819	1916820	A	C	27	GENIC	homozygous	139853355
16	1917246	1917246		GGATG	27	GENIC	homozygous	139817052
16	1917247	1917248	C	T	25	GENIC	homozygous	139853356
16	1918136	1918137	A	G	26	GENIC	homozygous	139853360
16	1917655	1917656	T	C	19	GENIC	homozygous	139853357
16	1917731	1917732	G	A	20	GENIC	homozygous	139853358
16	1918040	1918041	G	A	29	GENIC	homozygous	139853359
16	1918205	1918206	G	A	24	GENIC	homozygous	139853361
16	1918738	1918739	A	G	13	GENIC	homozygous	139853362
16	1918750	1918751	A	C	15	GENIC	homozygous	139853363
16	1918759	1918759		A	11	GENIC	homozygous	139817053
16	1918905	1918906	C	T	22	GENIC	homozygous	139853364
16	1919379	1919380	G	A	26	GENIC	homozygous	139853365
16	1919687	1919688	T	C	21	GENIC	homozygous	139853366
16	1920034	1920035	C	T	18	GENIC	homozygous	139853367
16	1920166	1920167	A	G	26	GENIC	homozygous	139853368
16	1920373	1920374	T	G	19	GENIC	homozygous	139853369
16	1920724	1920725	A	G	18	GENIC	homozygous	139853370
16	1920981	1920993	TTAAAATGAGTT		17	GENIC	homozygous	139817054
16	1921106	1921107	A	G	19	GENIC	homozygous	139853371
16	1921338	1921338		T	32	GENIC	homozygous	139817055
16	1922661	1922662	A	G	18	GENIC	homozygous	139853372
16	1923042	1923043	G	A	23	GENIC	homozygous	139853373
16	1923665	1923666	C	A	16	GENIC	homozygous	139853374
16	1923867	1923868	T		16	GENIC	homozygous	139817056
16	1925026	1925027	T	C	25	GENIC	homozygous	139853375
16	1925226	1925227	A	T	21	GENIC	possibly homozygous	139853376