chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	44114654	44114655	G	A	46	GENIC	homozygous	83906593
14	44114656	44114657	G	A	45	GENIC	homozygous	65948314
14	44114808	44114809	T	C	37	GENIC	homozygous	83906594
14	44114956	44114957	A	G	37	GENIC	homozygous	65948318
14	44115001	44115002	G	T	37	GENIC	homozygous	66501481
14	44115104	44115105	T	C	29	GENIC	homozygous	83906595
14	44115465	44115466	G	T	29	GENIC	homozygous	83906596
14	44116368	44116369	A	G	20	GENIC	possibly homozygous	65948330
14	44116760	44116761	A	G	33	GENIC	homozygous	65948336
14	44120206	44120207	C	T	23	GENIC	homozygous	83906597
14	44121590	44121591	G	A	22	GENIC	homozygous	65948360
14	44122017	44122018	C	T	26	GENIC	possibly homozygous	83906598
14	44122887	44122888	G	A	33	GENIC	homozygous	83906599
14	44123115	44123116	T	G	25	GENIC	homozygous	65948366
14	44123156	44123157	C	T	28	GENIC	homozygous	66445598
14	44124571	44124572	A	G	33	GENIC	homozygous	65948368