chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41173633	41173634	C	A	8	GENIC	homozygous	139144298
12	41173634	41173635	C	T	8	GENIC	homozygous	139144299
12	41173636	41173637	C	T	8	GENIC	homozygous	139144300
12	41173639	41173640	C	T	8	GENIC	homozygous	139144301
12	41173641	41173642	C	T	9	GENIC	homozygous	139144302
12	41173643	41173644	C	T	8	GENIC	homozygous	139144303
12	41173647	41173648	C	T	8	GENIC	homozygous	139144304
12	41173650	41173651	C	T	8	GENIC	homozygous	139144305
12	41173658	41173659	C	T	8	GENIC	homozygous	139144306
12	41173663	41173664	C	T	8	GENIC	homozygous	139144307
12	41173666	41173667	C	T	9	GENIC	homozygous	139144308
12	41175706	41175707	G	T	55	GENIC	homozygous	144923716
12	41184885	41184886	C		10	GENIC	homozygous	139056577