chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	102941599	102941600	T	C	39	GENIC	homozygous	109115427
1	102944242	102944243	A	G	39	GENIC	homozygous	109115429
1	102945598	102945599	C	T	51	GENIC	homozygous	109115433
1	102946046	102946047	A	G	49	GENIC	homozygous	120503647
1	102946047	102946048	T	A	51	GENIC	homozygous	120503648
1	102947136	102947137	T	A	46	GENIC	homozygous	109115435
1	102947607	102947608	T	C	53	GENIC	homozygous	109115437
1	102947653	102947654	T	A	59	GENIC	homozygous	109115439
1	102948656	102948656		A	43	GENIC	homozygous	130818479
1	102947528	102947528		C	55	GENIC	homozygous	130818477
1	102947579	102947579		C	46	GENIC	homozygous	130818478
1	102950349	102950350	C	T	54	GENIC	homozygous	109115441
1	102953494	102953495	C	T	45	GENIC	homozygous	109115443
1	102954626	102954627	C	T	47	GENIC	homozygous	109115447
1	102957497	102957498	T	C	60	GENIC	homozygous	109115449
1	102958021	102958022	A	T	49	GENIC	homozygous	109115451
1	102958165	102958166	C	T	44	GENIC	possibly homozygous	109115453
1	102958201	102958202	A	G	51	GENIC	possibly homozygous	109115455
1	102960758	102960759	A	G	52	GENIC	homozygous	109115457
1	102965291	102965292	T	C	42	GENIC	homozygous	109115459
1	102968260	102968261	T	A	51	GENIC	homozygous	109115461
1	102969965	102969965		AGGAGGAGG	37	GENIC	possibly homozygous	130818480
1	102965533	102965534	C	T	22	GENIC	homozygous	130843637