chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13551262	13551263	A	T	10	GENIC	homozygous	116496232
10	13553541	13553541		G	12	GENIC	possibly homozygous	128790627
10	13555281	13555282	T	C	19	GENIC	homozygous	116496234
10	13555682	13555683	T	C	16	GENIC	homozygous	116496236
10	13555711	13555712	A	G	19	GENIC	homozygous	116496238
10	13556946	13556949	CTT		17	GENIC	homozygous	128790628
10	13557289	13557290	G	T	22	GENIC	homozygous	116496240
10	13559231	13559232	A		14	GENIC	homozygous	128790629
10	13561902	13561903	G		15	GENIC	homozygous	128790630
10	13562048	13562049	C	T	16	GENIC	homozygous	116496250
10	13558699	13558700	G	A	32	GENIC	homozygous	116496242
10	13558709	13558710	A	G	30	GENIC	homozygous	116496244
10	13560320	13560321	A	G	21	GENIC	homozygous	116496246
10	13561826	13561827	T	G	16	GENIC	homozygous	116496248
10	13563337	13563338	T	G	16	GENIC	homozygous	116496252
10	13563786	13563787	A		18	GENIC	homozygous	128790631
10	13564064	13564065	C	A	24	GENIC	possibly homozygous	116496254
10	13564135	13564136	A	G	24	GENIC	homozygous	116496256
10	13566455	13566456	A	C	18	GENIC	homozygous	116496264
10	13566580	13566580		GCTCTCTT	15	GENIC	homozygous	128790632
10	13567726	13567727	T	A	15	GENIC	possibly homozygous	116496266
10	13569080	13569081	C	T	21	GENIC	homozygous	116994656
10	13569532	13569533	A	G	34	GENIC	homozygous	116496268
10	13569693	13569694	T	C	23	GENIC	homozygous	116496270
10	13570110	13570111	C	T	28	GENIC	homozygous	116496272
10	13570229	13570229		TCCT	21	GENIC	homozygous	128790633
10	13570514	13570514		C	12	GENIC	possibly homozygous	128790634
10	13571357	13571358	C	T	19	GENIC	homozygous	116496274
10	13571411	13571412	G		14	GENIC	homozygous	128790635
10	13572029	13572030	G	T	22	GENIC	homozygous	116496276
10	13572387	13572387		GA	22	GENIC	homozygous	128790636
10	13573396	13573397	T	C	21	GENIC	homozygous	116496278
10	13574061	13574062	G	A	27	GENIC	homozygous	116496280
10	13574101	13574102	T	C	22	GENIC	homozygous	116496282
10	13564423	13564424	C	T	13	GENIC	homozygous	117294202