chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	93740462	93740463	A	G	28	GENIC	homozygous	114904749
6	93741251	93741252	C		27	GENIC	homozygous	128367987
6	93742792	93742793	A	C	36	GENIC	homozygous	114904751
6	93743371	93743371		C	31	GENIC	homozygous	128367989
6	93745226	93745227	T	C	10	GENIC	homozygous	126358339
6	93745765	93745766	A	T	41	GENIC	homozygous	114904753
6	93745780	93745782	AA		38	GENIC	homozygous	128367990
6	93745787	93745787		A	37	GENIC	homozygous	128367991
6	93745789	93745789		A	38	GENIC	homozygous	128367992
6	93745813	93745814	G		44	GENIC	homozygous	128367993
6	93745825	93745825		T	49	GENIC	homozygous	128367994
6	93745923	93745924	G		46	GENIC	homozygous	128367995
6	93745931	93745931		A	48	GENIC	homozygous	128367996
6	93745974	93745975	A	C	41	GENIC	homozygous	114904755
6	93745977	93745978	A	T	41	GENIC	homozygous	114904757
6	93745979	93745980	C	G	41	GENIC	homozygous	114904759
6	93745980	93745981	C	G	42	GENIC	homozygous	114904761
6	93746171	93746171		C	27	GENIC	homozygous	128367997
6	93746175	93746181	ACTTAA		27	GENIC	homozygous	128367998
6	93746640	93746640		ATGGTTGTGAGCCACCATGTGGTTGCTAGGAATTGAACTCAGGACCTCTGGAAGAGCAGTCAGTGCTCTTAACCACTGAGTCATCTCTCC	23	GENIC	homozygous	128367999
6	93747220	93747221	T	G	50	GENIC	homozygous	114904763
6	93747856	93747857	A	G	53	GENIC	possibly homozygous	114904771
6	93749148	93749149	T	C	55	GENIC	possibly homozygous	114904773
6	93748749	93748750	T	C	50	GENIC	homozygous	115139515
6	93746171	93746172	T	A	27	GENIC	homozygous	118554921
6	93747113	93747114	C	T	45	GENIC	homozygous	115139514