chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	102941599	102941600	T	C	14	GENIC	possibly homozygous	109115427
1	102944242	102944243	A	G	20	GENIC	homozygous	109115429
1	102945598	102945599	C	T	19	GENIC	homozygous	109115433
1	102946046	102946047	A	G	11	GENIC	homozygous	120503647
1	102946047	102946048	T	A	11	GENIC	homozygous	120503648
1	102947136	102947137	T	A	17	GENIC	homozygous	109115435
1	102947607	102947608	T	C	20	GENIC	homozygous	109115437
1	102947653	102947654	T	A	15	GENIC	homozygous	109115439
1	102947528	102947528		C	30	GENIC	homozygous	130818477
1	102947579	102947579		C	22	GENIC	homozygous	130818478
1	102948656	102948656		A	15	GENIC	homozygous	130818479
1	102950349	102950350	C	T	22	GENIC	homozygous	109115441
1	102953494	102953495	C	T	16	GENIC	homozygous	109115443
1	102954626	102954627	C	T	17	GENIC	homozygous	109115447
1	102957497	102957498	T	C	17	GENIC	homozygous	109115449
1	102958021	102958022	A	T	22	GENIC	homozygous	109115451
1	102958165	102958166	C	T	25	GENIC	homozygous	109115453
1	102958201	102958202	A	G	18	GENIC	homozygous	109115455
1	102960758	102960759	A	G	15	GENIC	homozygous	109115457
1	102965291	102965292	T	C	25	GENIC	homozygous	109115459
1	102968260	102968261	T	A	20	GENIC	homozygous	109115461
1	102969965	102969965		AGGAGGAGG	16	GENIC	homozygous	130818480
1	102965533	102965534	C	T	20	GENIC	homozygous	130843637
1	102965559	102965560	C	T	20	GENIC	heterozygous	132444843