chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	71405668	71405669	T	C	23	GENIC	homozygous	117718248
9	71408210	71408211	C	T	20	GENIC	homozygous	117737898
9	71408829	71408830	A	G	38	GENIC	homozygous	117737900
9	71408891	71408892	T	C	33	GENIC	homozygous	117737902
9	71410127	71410128	T	C	23	GENIC	homozygous	117737904
9	71410386	71410387	A	G	16	GENIC	possibly homozygous	117718262
9	71415393	71415394	G	A	38	GENIC	homozygous	117718272
9	71415727	71415728	G	A	24	GENIC	homozygous	117737910
9	71417941	71417942	A	C	19	GENIC	homozygous	117737912
9	71418961	71418962	G	T	38	GENIC	homozygous	117718276
9	71420396	71420397	T	C	30	GENIC	homozygous	117718278
9	71425529	71425530	T	C	23	GENIC	homozygous	117718288
9	71426411	71426412	G	C	31	GENIC	homozygous	117737920
9	71427459	71427460	T	C	21	GENIC	homozygous	117718298
9	71428402	71428403	T	G	36	GENIC	homozygous	117718304
9	71431410	71431411	C	T	18	GENIC	possibly homozygous	117737926
9	71432064	71432065	T	C	26	GENIC	homozygous	117737928
9	71432108	71432109	A	G	23	GENIC	homozygous	117718310
9	71433115	71433116	C	T	19	GENIC	homozygous	117737932
9	71433870	71433871	T	C	22	GENIC	homozygous	117718312