chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45060554	45060555	C	T	21	GENIC	homozygous	51441652
10	45060662	45060663	T	A	24	GENIC	homozygous	51441655
10	45060879	45060880	G	-	24	GENIC	homozygous	51441656
10	45061589	45061590	G	A	39	GENIC	homozygous	51441657
10	45061770	45061771	C	A	47	GENIC	homozygous	51441658
10	45062481	45062482	G	A	42	GENIC	homozygous	51441659
10	45062861	45062865	TCTC	----	16	GENIC	homozygous	51441660
10	45062888	45062889	T	TTC	15	GENIC	homozygous	51441662
10	45062931	45062932	T	C	16	GENIC	homozygous	51441663
10	45063002	45063003	G	GGTGTGT	2	GENIC	homozygous	52372829
10	45063070	45063071	T	TGC	25	GENIC	homozygous	51441664
10	45063074	45063075	A	-	27	GENIC	homozygous	51441665
10	45063076	45063077	A	G	28	GENIC	homozygous	52372832
10	45064023	45064024	C	T	47	GENIC	homozygous	51441666
10	45064711	45064721	AAAAAAAAAA	----------	24	GENIC	homozygous	51441667
10	45066883	45066884	T	TTGGTTTCCGACCTGC	16	GENIC	homozygous	52372834
10	45066885	45066886	A	AACTGAGCCTACACAAGATGACAGGTAAGCAG	16	GENIC	homozygous	52372836
10	45067232	45067233	G	A	38	GENIC	homozygous	51441668
10	45067839	45067840	A	AGAGGGAGGGAGGGAGG	2	GENIC	homozygous	52372838
10	45069783	45069784	C	A	36	GENIC	homozygous	51441670
10	45070445	45070446	T	C	44	GENIC	homozygous	51441671
10	45070557	45070558	G	A	31	GENIC	homozygous	51441672