chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	83891111	83891112	T	C	25	GENIC	homozygous	113501687
14	83904697	83904698	G	A	37	GENIC	homozygous	113605147
14	83904716	83904717	T	A	31	GENIC	homozygous	113605148
14	83904736	83904737	G	A	36	GENIC	homozygous	113605149
14	83904738	83904739	G	A	37	GENIC	homozygous	113605150
14	83904740	83904741	A	C	38	GENIC	homozygous	113605151
14	83904745	83904746	C	A	39	GENIC	homozygous	113605152
14	83904755	83904756	G	A	37	GENIC	homozygous	113605153
14	83904761	83904762	A	C	39	GENIC	homozygous	113605154
14	83904763	83904764	G	A	38	GENIC	homozygous	113605155
14	83904781	83904782	T	C	38	GENIC	homozygous	113605156
14	83904793	83904794	A	T	42	GENIC	homozygous	113605157
14	83904813	83904814	G	A	43	GENIC	homozygous	113501691
14	83904819	83904820	T	C	42	GENIC	homozygous	113501693
14	83911061	83911062	A	G	26	GENIC	homozygous	113605161
14	83925815	83925816	C	A	12	GENIC	homozygous	113501695
14	83917973	83917974	G	A	19	GENIC	heterozygous	114099307