chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	11034210	11034211	T	C	28	GENIC	homozygous	117804133
9	11035361	11035362	C	T	11	GENIC	homozygous	117244468
9	11036617	11036618	T	G	19	GENIC	homozygous	117244469
9	11036726	11036727	A	C	9	GENIC	homozygous	117244470
9	11037133	11037134	T	G	24	GENIC	homozygous	117244472
9	11037171	11037172	G	C	20	GENIC	homozygous	117244473
9	11037192	11037193	T	A	12	GENIC	homozygous	117244474
9	11037199	11037200	C	T	17	GENIC	homozygous	117244475
9	11037380	11037381	C	G	6	GENIC	homozygous	117244476
9	11037382	11037383	C	A	6	GENIC	homozygous	117244477
9	11037427	11037428	G	C	12	GENIC	homozygous	117244478
9	11037541	11037542	G	T	6	GENIC	homozygous	117244479
9	11038250	11038251	T	G	18	GENIC	homozygous	117244480
9	11038426	11038427	C	A	18	GENIC	homozygous	117244481
9	11038436	11038437	C	T	18	GENIC	homozygous	117244482
9	11047500	11047501	A	G	25	GENIC	homozygous	117804134
9	11048442	11048443	A	G	18	GENIC	homozygous	117804135
9	11048774	11048775	T	C	25	GENIC	homozygous	117804136
9	11049320	11049321	G	A	31	GENIC	homozygous	117804137
9	11051308	11051309	T	C	30	GENIC	homozygous	117804138
9	11054865	11054866	T	G	39	GENIC	homozygous	117804139