chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	103396337	103396338	G	A	20	GENIC	homozygous	114694581
13	103396480	103396481	C	T	30	GENIC	homozygous	114694582
13	103397346	103397347	G	C	37	GENIC	homozygous	114438013
13	103397371	103397372	C	T	33	GENIC	homozygous	114438017
13	103397651	103397652	C	A	28	GENIC	homozygous	114438019
13	103398168	103398169	T	C	26	GENIC	homozygous	114694583
13	103398556	103398557	C	T	18	GENIC	homozygous	114588830
13	103398823	103398824	A	T	29	GENIC	homozygous	114694584
13	103398891	103398892	G	A	32	GENIC	homozygous	114694585
13	103398977	103398978	C	T	41	GENIC	homozygous	114694586
13	103400842	103400843	T	C	35	GENIC	homozygous	114588832
13	103402997	103402998	T	C	30	GENIC	homozygous	114694587
13	103403005	103403006	T	C	29	GENIC	homozygous	114694588
13	103403065	103403066	G	A	30	GENIC	homozygous	114694589
13	103403237	103403238	T	C	40	GENIC	homozygous	114694590
13	103403552	103403553	A	G	22	GENIC	homozygous	114588848
13	103404127	103404128	C	T	24	GENIC	homozygous	114694591
13	103404152	103404153	T	C	26	GENIC	homozygous	114694592
13	103404194	103404195	T	G	26	GENIC	homozygous	114588850
13	103404213	103404214	T	C	29	GENIC	homozygous	114694593
13	103404313	103404314	C	T	30	GENIC	homozygous	114694594
13	103404334	103404335	C	T	26	GENIC	homozygous	114694595
13	103404436	103404437	A	G	42	GENIC	homozygous	114694596
13	103405054	103405055	G	A	15	GENIC	homozygous	114694597
13	103405061	103405062	G	A	16	GENIC	homozygous	114694598
13	103406473	103406474	G	A	24	GENIC	homozygous	114694599
13	103406709	103406710	A	G	37	GENIC	homozygous	114694600
13	103401273	103401274	G	A	15	GENIC	homozygous	115018532
13	103401292	103401293	C	A	18	GENIC	homozygous	115018534
13	103401395	103401396	C	G	11	GENIC	homozygous	115018536