chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	124025590	124025591	A	G	19	GENIC	homozygous	115864596
7	124026985	124026986	A	C	14	GENIC	homozygous	115864598
7	124027202	124027203	A		16	GENIC	homozygous	128514193
7	124027604	124027605	A	G	21	GENIC	homozygous	115864600
7	124027664	124027665	C	T	23	GENIC	homozygous	115864602
7	124028018	124028019	T	C	22	GENIC	homozygous	115864604
7	124029142	124029143	T	C	20	GENIC	homozygous	115864606
7	124029411	124029412	A	G	19	GENIC	homozygous	115864608
7	124029635	124029636	A	G	26	GENIC	homozygous	115864610
7	124029662	124029663	T	C	26	GENIC	homozygous	115864612
7	124036144	124036145	G	T	16	GENIC	homozygous	115864614
7	124036353	124036354	T	C	22	GENIC	homozygous	115864616
7	124036622	124036623	G	C	10	GENIC	homozygous	115864618
7	124036639	124036650	ACCAAGTTGAC		10	GENIC	homozygous	128514194
7	124039590	124039600	AAGTGGGAGG		15	GENIC	homozygous	128514195
7	124039678	124039679	G	A	18	GENIC	homozygous	115864626
7	124036671	124036672	A	G	11	GENIC	homozygous	115864620
7	124037519	124037520	A	G	10	GENIC	possibly homozygous	115864622
7	124039001	124039002	A	G	26	GENIC	homozygous	115864624
7	124040677	124040678	A		8	GENIC	homozygous	128514196
7	124040712	124040713	T	A	15	GENIC	homozygous	115864628
7	124041414	124041415	A	G	21	GENIC	homozygous	115864630