chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	80273589	80273590	A	G	18	GENIC	homozygous	109298504
1	80274858	80274859	C	T	28	GENIC	homozygous	120481170
1	80276284	80276285	A	G	32	GENIC	homozygous	109298506
1	80277440	80277441	T	C	24	GENIC	homozygous	120779162
1	80278277	80278278	C	T	24	GENIC	homozygous	120481171
1	80278767	80278768	T	C	32	GENIC	homozygous	109298514
1	80279623	80279624	T	C	27	GENIC	possibly homozygous	109298518
1	80282887	80282888	T	C	15	GENIC	homozygous	109298526
1	80283877	80283878	A	C	22	GENIC	homozygous	109298528
1	80284222	80284223	A	G	15	GENIC	homozygous	120481174
1	80284712	80284713	C	G	22	GENIC	homozygous	120481175
1	80284790	80284791	C	A	21	GENIC	homozygous	120779163
1	80284829	80284830	G	A	17	GENIC	homozygous	120481176
1	80285137	80285138	G	A	17	GENIC	homozygous	109298535
1	80285215	80285216	G	A	28	GENIC	homozygous	120481177
1	80285392	80285393	A	G	21	GENIC	homozygous	109298537
1	80286009	80286010	T	A	27	GENIC	homozygous	120481178
1	80287075	80287076	A	G	23	GENIC	possibly homozygous	109298547
1	80287780	80287781	C	G	18	GENIC	homozygous	109298549
1	80288928	80288929	G	A	29	GENIC	homozygous	120481179
1	80290339	80290340	T	C	28	GENIC	possibly homozygous	109298553