chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	44714378	44714379	C	T	75	GENIC	heterozygous	117822914
9	44714501	44714502	C	T	68	GENIC	heterozygous	117822915
9	44714607	44714608	C	T	68	GENIC	heterozygous	117822916
9	44749989	44749990	T	C	92	GENIC	heterozygous	117333727
9	44750038	44750039	C	A	100	GENIC	heterozygous	117333728
9	44750110	44750111	C	T	72	GENIC	heterozygous	117505412
9	44750129	44750130	C	T	75	GENIC	heterozygous	117723135
9	44750146	44750147	T	C	81	GENIC	heterozygous	117333729
9	44750193	44750194	C	T	69	GENIC	heterozygous	117333730
9	44750203	44750204	C	A	69	GENIC	heterozygous	117333731
9	44750237	44750238	A	C	64	GENIC	heterozygous	117333732
9	44750337	44750338	A	C	81	GENIC	heterozygous	117333733
9	44750489	44750490	T	C	64	GENIC	heterozygous	117723141
9	44750593	44750594	T	C	45	GENIC	heterozygous	117333734
9	44750595	44750596	C	T	47	GENIC	heterozygous	117333735
9	44750688	44750689	A	C	48	GENIC	heterozygous	117333736
9	44750705	44750706	C	A	45	GENIC	heterozygous	117333737
9	44770142	44770143	G	A	50	GENIC	possibly homozygous	117333738
9	44781800	44781801	A	G	22	GENIC	possibly homozygous	117333739
9	44750496	44750497	C	T	58	GENIC	heterozygous	117723143
9	44750506	44750507	T	C	56	GENIC	heterozygous	117723145