chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	45045331	45045332	T	G	22	GENIC	homozygous	114719579
13	45050815	45050816	T	C	33	GENIC	homozygous	114547601
13	45051058	45051059	C	T	31	GENIC	homozygous	114547602
13	45051148	45051149	G	A	24	GENIC	homozygous	114719581
13	45053144	45053145	G	A	18	GENIC	homozygous	114719583
13	45055376	45055377	C	T	7	GENIC	homozygous	114547612
13	45056578	45056579	C	G	21	GENIC	homozygous	114719587
13	45059879	45059880	G	C	19	GENIC	homozygous	114719589
13	45060523	45060524	C	T	9	GENIC	homozygous	114719591
13	45061899	45061900	T	C	29	GENIC	homozygous	114719593
13	45062613	45062614	A	C	10	GENIC	homozygous	114547627
13	45062948	45062949	A	G	12	GENIC	homozygous	114547628
13	45063352	45063353	T	G	13	GENIC	homozygous	114719596
13	45063602	45063603	A	G	20	GENIC	homozygous	114547629
13	45064674	45064675	A	G	30	GENIC	homozygous	114547632
13	45064878	45064879	G	T	12	GENIC	homozygous	114547634
13	45065287	45065288	A	G	18	GENIC	homozygous	114547641
13	45065640	45065641	A	G	22	GENIC	homozygous	114719598
13	45067212	45067213	A	G	20	GENIC	homozygous	114547645
13	45058426	45058427	A	G	15	GENIC	homozygous	115099440
13	45067576	45067577	T	C	7	GENIC	homozygous	115099442
13	45059843	45059844	T	C	23	GENIC	homozygous	114612422