chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	102638068	102638069	C	T	59	GENIC	homozygous	114586924
13	102638948	102638949	C	A	46	GENIC	homozygous	114694049
13	102638969	102638970	A	G	45	GENIC	homozygous	114694050
13	102639226	102639227	C	T	8	GENIC	homozygous	118507081
13	102639255	102639256	T	C	10	GENIC	heterozygous	118529560
13	102639837	102639838	G	A	38	GENIC	homozygous	114694051
13	102639868	102639868		A	35	GENIC	homozygous	132714871
13	102639640	102639641	G		10	GENIC	homozygous	132714870
13	102640101	102640102	G	A	10	GENIC	homozygous	118529561
13	102640181	102640181		T	33	GENIC	homozygous	132714873
13	102640593	102640594	T	C	55	GENIC	homozygous	114586932
13	102640724	102640725	G	A	61	GENIC	homozygous	114586934
13	102641270	102641271	C	G	22	GENIC	homozygous	114586936
13	102641292	102641293	A	T	20	GENIC	homozygous	132178344
13	102641286	102641287	A	T	21	GENIC	homozygous	132178341
13	102641288	102641289	A	T	22	GENIC	homozygous	132178342
13	102641290	102641291	A	T	21	GENIC	homozygous	132178343
13	102641294	102641295	A	T	20	GENIC	homozygous	132178345
13	102641296	102641297	A	T	21	GENIC	homozygous	132178346
13	102641298	102641299	A	T	21	GENIC	homozygous	132178347
13	102641300	102641301	A	T	22	GENIC	homozygous	132178348
13	102641302	102641303	A	T	23	GENIC	homozygous	132178349
13	102641304	102641305	A	T	23	GENIC	homozygous	132178350
13	102642306	102642307	A		58	GENIC	homozygous	132714874
13	102642362	102642363	A	T	52	GENIC	homozygous	114586938
13	102642450	102642451	G	C	44	GENIC	homozygous	114586940
13	102642611	102642612	C	T	40	GENIC	homozygous	114694052
13	102642790	102642791	T	G	45	GENIC	homozygous	114694053