chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9236256	9236257	C	T	37	GENIC	homozygous	130048733
20	9236557	9236558	G	A	28	GENIC	homozygous	130048738
20	9236610	9236611	C	A	31	GENIC	homozygous	130048741
20	9236749	9236750	T	C	45	GENIC	homozygous	130048744
20	9236831	9236832	C	T	34	GENIC	homozygous	130048750
20	9236844	9236845	A	G	37	GENIC	homozygous	130048752
20	9237042	9237043	C	T	40	GENIC	homozygous	143720326
20	9237101	9237102	C	T	37	GENIC	homozygous	143720327
20	9237267	9237268	C	T	40	GENIC	homozygous	130048755
20	9237485	9237486	G	A	45	GENIC	homozygous	143720328
20	9237537	9237538	T	C	52	GENIC	homozygous	143720329
20	9237658	9237659	G	A	49	GENIC	homozygous	140514472
20	9237683	9237684	G	A	47	GENIC	homozygous	143720330
20	9237891	9237892	T	A	38	GENIC	homozygous	143720331
20	9237904	9237911	GGAGCTG		34	GENIC	homozygous	140484575
20	9239233	9239234	T	C	38	GENIC	homozygous	130048761
20	9239282	9239283	T	C	38	GENIC	homozygous	130048764
20	9239292	9239293	C	G	43	GENIC	homozygous	130048767
20	9238386	9238387	G		2	GENIC	homozygous	143710641