chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	49441648	49441649	C	G	34	GENIC	homozygous	116488361
8	49441731	49441732	T	C	31	GENIC	homozygous	116488363
8	49443110	49443111	A	G	37	GENIC	homozygous	116488365
8	49443245	49443246	A	G	38	GENIC	homozygous	116488367
8	49444274	49444275	C	G	29	GENIC	homozygous	117961854
8	49444569	49444570	G	A	22	GENIC	homozygous	117961855
8	49444661	49444662	C	T	21	GENIC	homozygous	117961856
8	49444743	49444744	A	T	32	GENIC	homozygous	116488371
8	49446795	49446796	T	C	27	GENIC	homozygous	116488377
8	49448903	49448904	A	G	25	GENIC	homozygous	116488381
8	49449283	49449284	A	G	32	GENIC	homozygous	117961857
8	49449354	49449355	T	G	23	GENIC	homozygous	117961858
8	49450353	49450354	A	G	31	GENIC	homozygous	117961859
8	49450671	49450672	G	A	20	GENIC	homozygous	116488383
8	49450672	49450673	T	C	19	GENIC	homozygous	116488385
8	49450720	49450721	C	T	19	GENIC	homozygous	117961860
8	49452161	49452162	G	A	13	GENIC	homozygous	117961861
8	49452303	49452304	T	C	19	GENIC	homozygous	117961862
8	49454314	49454315	C	T	19	GENIC	homozygous	117961863
8	49455615	49455616	G	A	25	GENIC	homozygous	117961864