chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90937217	90937218	A	G	6	GENIC	homozygous	51738271
10	90939820	90939821	G	A	7	GENIC	homozygous	51738279
10	90940197	90940198	G	GA	2	GENIC	heterozygous	51738281
10	90940262	90940263	C	T	1	GENIC	homozygous	52996723
10	90941296	90941297	C	A	6	GENIC	homozygous	52996725
10	90941861	90941862	G	A	11	GENIC	heterozygous	52996727
10	90942630	90942631	A	G	23	GENIC	homozygous	52996729
10	90942865	90942866	C	T	23	GENIC	homozygous	52996731
10	90943204	90943205	A	G	10	GENIC	homozygous	52165942
10	90943385	90943386	T	TGAG	8	GENIC	homozygous	52165943
10	90943656	90943657	T	C	12	GENIC	homozygous	52996733
10	90943681	90943682	G	A	11	GENIC	homozygous	52996735
10	90943829	90943830	G	C	7	GENIC	heterozygous	52996738
10	90943975	90943976	A	G	12	GENIC	homozygous	52996740
10	90944249	90944250	A	G	2	GENIC	homozygous	52996742
10	90944372	90944373	C	T	14	GENIC	possibly homozygous	52996744
10	90944539	90944540	T	C	9	GENIC	heterozygous	52996746
10	90944553	90944554	C	T	5	GENIC	homozygous	52996748
10	90946158	90946159	T	C	17	GENIC	homozygous	51538761
10	90949349	90949350	G	GC	2	GENIC	heterozygous	51738294
10	90953339	90953340	A	G	8	GENIC	homozygous	51738317
10	90955906	90955907	G	C	8	GENIC	heterozygous	52996750
10	90956391	90956394	CCC	---	1	GENIC	homozygous	52165953
10	90956505	90956506	T	C	14	GENIC	possibly homozygous	51738323
10	90947896	90947897	C	A	1	GENIC	homozygous	51997628