chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	103397346	103397347	G	C	29	GENIC	homozygous	114438013
13	103397351	103397352	C	A	29	GENIC	possibly homozygous	114438015
13	103397371	103397372	C	T	32	GENIC	homozygous	114438017
13	103397644	103397645	C	A	18	GENIC	homozygous	118467719
13	103397645	103397646	C	G	18	GENIC	homozygous	118467720
13	103397646	103397647	C	G	18	GENIC	homozygous	118467721
13	103397647	103397648	C	G	18	GENIC	homozygous	118467722
13	103397651	103397652	C	A	19	GENIC	homozygous	114438019
13	103399438	103399439	C	T	36	GENIC	homozygous	118467724
13	103399475	103399476	C	T	24	GENIC	homozygous	118467725
13	103399544	103399545	A	C	22	GENIC	homozygous	118467726
13	103400747	103400748	G	T	32	GENIC	homozygous	114438021
13	103400886	103400887	T	G	35	GENIC	homozygous	114588834
13	103400963	103400964	C	T	8	GENIC	homozygous	118467727
13	103399418	103399419	T	G	38	GENIC	homozygous	118551056
13	103401272	103401273	A	G	41	GENIC	homozygous	114438027
13	103401418	103401419	T	A	48	GENIC	homozygous	114725661
13	103401273	103401274	G	A	42	GENIC	homozygous	115018532
13	103401292	103401293	C	A	34	GENIC	homozygous	115018534
13	103402508	103402509	T	C	44	GENIC	heterozygous	118551057
13	103402628	103402629	C	T	45	GENIC	heterozygous	118467728
13	103402667	103402668	C	T	17	GENIC	heterozygous	118467729
13	103402670	103402671	C	T	14	GENIC	heterozygous	118551058
13	103402676	103402677	C	T	8	GENIC	homozygous	118467730
13	103402751	103402752	A	T	8	GENIC	homozygous	118467732
13	103402763	103402764	C	T	11	GENIC	homozygous	118467733