chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90379787	90379788	A	G	19	GENIC	homozygous	114574392
13	90383118	90383119	T	C	23	GENIC	homozygous	114574394
13	90385661	90385662	C	T	28	GENIC	homozygous	114574396
13	90388031	90388032	T	C	11	GENIC	homozygous	114574398
13	90388685	90388686	T	A	20	GENIC	homozygous	114574400
13	90388698	90388699	G	A	19	GENIC	homozygous	114574402
13	90388766	90388767	G	A	18	GENIC	homozygous	114574404
13	90389065	90389066	G	A	11	GENIC	homozygous	114574406
13	90390732	90390733	A	G	16	GENIC	homozygous	114574408
13	90397302	90397303	T	C	18	GENIC	homozygous	114574411
13	90397575	90397576	T	C	9	GENIC	homozygous	114574413
13	90397757	90397758	A	G	21	GENIC	homozygous	114574415
13	90401643	90401644	A	G	20	GENIC	homozygous	114574417
13	90401941	90401942	G	A	22	GENIC	homozygous	114574419
13	90402424	90402425	T	G	22	GENIC	homozygous	114574421
13	90402989	90402990	G	A	17	GENIC	homozygous	114574423
13	90404717	90404718	A	T	17	GENIC	homozygous	114574425