chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	101608987	101608987		A	15	GENIC	heterozygous	140903579
10	101628153	101628153		T	20	GENIC	homozygous	146494024
10	101629292	101629293	T	C	26	GENIC	homozygous	146495310
10	101628160	101628161	A	T	21	GENIC	homozygous	146495307
10	101628228	101628229	T	C	23	GENIC	homozygous	146495308
10	101628435	101628436	G	A	25	GENIC	homozygous	146495309
10	101630248	101630249	G	A	33	GENIC	homozygous	146495311
10	101630362	101630363	T		22	GENIC	homozygous	146494025
10	101630398	101630399	A	T	28	GENIC	homozygous	146495312
10	101631329	101631330	T	A	28	GENIC	homozygous	146495313
10	101631330	101631331	C	T	28	GENIC	homozygous	146495314
10	101631336	101631337	T	A	28	GENIC	homozygous	146495315
10	101631680	101631681	C	A	20	GENIC	homozygous	146495316
10	101632275	101632276	G	A	24	GENIC	homozygous	146495317
10	101632330	101632331	A	C	34	GENIC	homozygous	146495318
10	101632530	101632531	T	C	28	GENIC	homozygous	146495319
10	101633735	101633736	G	A	23	GENIC	homozygous	146495320
10	101634356	101634357	A	G	15	GENIC	homozygous	146495321
10	101634804	101634805	C	A	1	GENIC	homozygous	146495322
10	101635147	101635148	C	T	10	GENIC	homozygous	146495323
10	101635189	101635194	ATTTA		9	GENIC	homozygous	146494026
10	101635243	101635244	T	C	10	GENIC	homozygous	146495324
10	101635260	101635261	T	C	12	GENIC	homozygous	143469190
10	101635968	101635968		T	13	GENIC	homozygous	146494027
10	101636403	101636404	G	C	23	GENIC	homozygous	146495325
10	101636496	101636497	G	A	24	GENIC	homozygous	146495326
10	101636694	101636695	C	T	7	GENIC	homozygous	146495327
10	101637622	101637623	A	G	28	GENIC	homozygous	146495328
10	101637942	101637943	A	G	34	GENIC	homozygous	146495329
10	101638776	101638776		A	25	GENIC	possibly homozygous	146494028
10	101633238	101633238		C	15	GENIC	heterozygous	144079764
10	101634639	101634640	T	C	10	GENIC	homozygous	154671700
10	101634793	101634793		A	1	GENIC	homozygous	138702628