chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	121099787	121099788	T	G	12	GENIC	homozygous	54085603
7	121101350	121101351	G	A	15	GENIC	homozygous	54085604
7	121101382	121101383	C	-	11	GENIC	homozygous	54085605
7	121101641	121101642	T	-	9	GENIC	homozygous	54921186
7	121101643	121101644	T	-	9	GENIC	homozygous	54085607
7	121101645	121101646	T	G	10	GENIC	homozygous	54921188
7	121101659	121101660	T	G	14	GENIC	homozygous	54085609
7	121102443	121102444	T	C	11	GENIC	homozygous	54085610
7	121104272	121104273	T	C	11	GENIC	homozygous	54085611
7	121105519	121105520	A	G	9	GENIC	homozygous	54085612
7	121106032	121106033	T	C	8	GENIC	homozygous	54085613
7	121106239	121106240	T	G	9	GENIC	homozygous	54085614
7	121107611	121107612	A	G	12	GENIC	homozygous	54085619
7	121108556	121108557	C	T	15	GENIC	homozygous	54085620
7	121109857	121109858	C	T	11	GENIC	homozygous	54085634
7	121110821	121110822	A	G	26	GENIC	homozygous	54085635
7	121111441	121111442	A	T	18	GENIC	homozygous	54085636
7	121111971	121111972	T	C	12	GENIC	homozygous	54085637
7	121112504	121112505	G	A	9	GENIC	homozygous	54085639
7	121111978	121111979	G	A	9	GENIC	homozygous	54085638
7	121113083	121113084	A	G	14	GENIC	homozygous	54085640
7	121114739	121114740	G	A	12	GENIC	homozygous	54085641
7	121115205	121115206	C	T	9	GENIC	homozygous	54085642
7	121118039	121118040	C	T	13	GENIC	homozygous	54085644
7	121118276	121118277	C	T	15	GENIC	homozygous	54085645