chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	37325682	37325683	C	T	11	GENIC	homozygous	53542174
10	37326498	37326499	C	T	7	GENIC	homozygous	53542175
10	37327505	37327506	T	G	10	GENIC	homozygous	52303107
10	37328838	37328839	A	G	9	GENIC	homozygous	51416677
10	37328980	37328981	T	-	14	GENIC	homozygous	53542176
10	37328998	37328999	C	T	16	GENIC	homozygous	52303116
10	37329586	37329587	T	TA	14	GENIC	homozygous	53542177
10	37329903	37329904	G	A	8	GENIC	homozygous	52303120
10	37330461	37330462	C	A	20	GENIC	homozygous	52303122
10	37330582	37330583	G	A	17	GENIC	homozygous	53542178
10	37330600	37330601	C	T	18	GENIC	homozygous	52303124
10	37331377	37331378	A	G	17	GENIC	homozygous	53542179
10	37331503	37331504	T	-	18	GENIC	homozygous	52303128
10	37332629	37332630	T	TC	14	GENIC	homozygous	52303132
10	37332798	37332799	A	C	18	GENIC	homozygous	51416683
10	37333647	37333648	G	T	13	GENIC	homozygous	53542180
10	37333648	37333649	C	T	13	GENIC	homozygous	53542181
10	37334576	37334577	T	TG	11	GENIC	homozygous	52303134
10	37335217	37335218	C	T	19	GENIC	homozygous	52303136
10	37335811	37335812	G	A	19	GENIC	homozygous	52303138
10	37336917	37336918	A	AGTTT	18	GENIC	homozygous	53542182
10	37337218	37337219	A	T	23	GENIC	homozygous	52303142
10	37337905	37337906	C	A	21	GENIC	homozygous	52303146
10	37339353	37339354	A	G	15	GENIC	homozygous	52041619
10	37339797	37339798	G	A	20	GENIC	homozygous	52041621
10	37340691	37340692	C	CTGGT	13	GENIC	homozygous	52041625
10	37341063	37341064	C	A	14	GENIC	possibly homozygous	52041627
10	37342494	37342495	C	T	10	GENIC	homozygous	52041635