chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41160615	41160617	AC		43	GENIC	heterozygous	141039498
12	41173633	41173634	C	A	18	GENIC	homozygous	139144298
12	41173634	41173635	C	T	17	GENIC	homozygous	139144299
12	41173636	41173637	C	T	16	GENIC	homozygous	139144300
12	41173639	41173640	C	T	15	GENIC	homozygous	139144301
12	41173641	41173642	C	T	15	GENIC	homozygous	139144302
12	41173643	41173644	C	T	15	GENIC	homozygous	139144303
12	41173647	41173648	C	T	14	GENIC	homozygous	139144304
12	41173650	41173651	C	T	13	GENIC	homozygous	139144305
12	41173658	41173659	C	T	7	GENIC	homozygous	139144306
12	41173663	41173664	C	T	9	GENIC	homozygous	139144307
12	41173666	41173667	C	T	8	GENIC	homozygous	139144308
12	41175697	41175698	G	T	45	GENIC	heterozygous	154745973
12	41184885	41184886	C		19	GENIC	homozygous	139056577
12	41175697	41175698	G		45	GENIC	homozygous	403327414
12	41175706	41175707	G	T	47	GENIC	homozygous	144923716
12	41198271	41198272	C		24	GENIC	heterozygous	403327416
12	41198271	41198272	C	G	24	GENIC	possibly homozygous	403327417
12	41198292	41198293	A		41	GENIC	heterozygous	403645908
12	41198292	41198293	A	T	41	GENIC	heterozygous	403645909
12	41216582	41216583	C	A	13	GENIC	heterozygous	139144381