chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	41738989	41738990	G	A	10	GENIC	homozygous	114921401
13	41739462	41739463	G	A	17	GENIC	homozygous	114921403
13	41740554	41740555	T	C	29	GENIC	homozygous	114329878
13	41740687	41740688	A	G	18	GENIC	homozygous	114921405
13	41741236	41741237	G	A	24	GENIC	homozygous	114921407
13	41741248	41741249	C	T	25	GENIC	homozygous	114921409
13	41743188	41743189	T	G	18	GENIC	homozygous	114921411
13	41743203	41743204	A	G	17	GENIC	homozygous	114329884
13	41743464	41743465	C	T	24	GENIC	homozygous	114921413
13	41744150	41744151	C	T	22	GENIC	homozygous	114921415
13	41744376	41744377	C	T	29	GENIC	homozygous	114921417
13	41745047	41745048	T	C	13	GENIC	homozygous	114921419
13	41745148	41745149	C	G	19	GENIC	homozygous	114921421
13	41745240	41745241	C	T	21	GENIC	homozygous	114921423
13	41745358	41745359	C	T	24	GENIC	homozygous	114921425
13	41745360	41745361	C	T	26	GENIC	homozygous	114921427
13	41746097	41746098	T	C	22	GENIC	homozygous	114921429
13	41746579	41746580	T	A	20	GENIC	homozygous	114921431
13	41746764	41746765	A	G	24	GENIC	homozygous	114921435
13	41747233	41747234	C	T	17	GENIC	homozygous	114329888
13	41747305	41747306	T	C	11	GENIC	homozygous	114329890
13	41748265	41748266	T	C	19	GENIC	homozygous	114921439
13	41748428	41748429	C	A	33	GENIC	homozygous	114329894
13	41749680	41749681	G	A	10	GENIC	homozygous	114329896
13	41750179	41750180	A	G	9	GENIC	homozygous	114921441
13	41750190	41750191	T	C	9	GENIC	homozygous	114921443
13	41752453	41752454	G	T	31	GENIC	homozygous	114921447
13	41752785	41752786	C	A	32	GENIC	homozygous	114921449
13	41755431	41755432	T	A	18	GENIC	homozygous	114329904
13	41756505	41756506	T	C	26	GENIC	homozygous	114921451
13	41757405	41757406	C	T	25	GENIC	homozygous	114921453