chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	56015829	56015830	T	G	4	GENIC	homozygous	114722100
13	56015831	56015832	T	G	4	GENIC	homozygous	114722102
13	56105721	56105722	C	G	13	GENIC	homozygous	114356120
13	56106247	56106248	G	A	18	GENIC	homozygous	114356126
13	56106248	56106249	A	T	18	GENIC	homozygous	114356128
13	56108308	56108309	C	G	28	GENIC	homozygous	114356142
13	56108320	56108321	C	A	37	GENIC	homozygous	114356144
13	56108322	56108323	A	T	37	GENIC	homozygous	114356146
13	56108337	56108338	A	G	36	GENIC	homozygous	114356148
13	56108340	56108341	C	A	36	GENIC	homozygous	114356150
13	56128296	56128297	A	G	12	GENIC	homozygous	115025028
13	56128647	56128648	T	G	9	GENIC	homozygous	114553415
13	56128648	56128649	A	T	9	GENIC	homozygous	114553416
13	56232006	56232007	A	T	17	GENIC	homozygous	114356340
13	56232007	56232008	C	A	16	GENIC	homozygous	114356342
13	56237738	56237739	T	C	27	GENIC	homozygous	114356360
13	56237739	56237740	T	C	27	GENIC	homozygous	114356362
13	56237740	56237741	T	G	28	GENIC	homozygous	114356364
13	56237743	56237744	T	C	28	GENIC	homozygous	114356366