chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13730639	13730640	G	A	79	GENIC	heterozygous	50062275
12	13730648	13730649	A	T	85	GENIC	heterozygous	50062277
12	13730692	13730693	A	T	91	GENIC	heterozygous	51057890
12	13730693	13730694	A	G	91	GENIC	heterozygous	51057891
12	13730694	13730695	C	G	91	GENIC	heterozygous	51057892
12	13730704	13730705	G	A	88	GENIC	heterozygous	51057893
12	13730705	13730706	T	C	87	GENIC	heterozygous	51057894
12	13730736	13730737	A	G	64	GENIC	heterozygous	50281359
12	13730738	13730739	G	T	63	GENIC	heterozygous	51057895
12	13730744	13730745	C	T	59	GENIC	heterozygous	51057896
12	13730747	13730748	C	T	55	GENIC	heterozygous	51057897
12	13730751	13730752	C	A	54	GENIC	heterozygous	51057898
12	13730755	13730756	C	T	51	GENIC	heterozygous	51057899
12	13731146	13731147	T	-	26	GENIC	heterozygous	50062281
12	13731310	13731311	C	CT	46	GENIC	heterozygous	50062283
12	13736634	13736635	T	C	40	GENIC	heterozygous	50281370
12	13736664	13736665	A	T	46	GENIC	heterozygous	50281371
12	13736758	13736759	A	G	30	GENIC	heterozygous	50281372
12	13740582	13740583	A	G	23	GENIC	heterozygous	50281391