chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	79021969	79021970	C	T	8	GENIC	homozygous	113239633
4	79021989	79021990	G	C	9	GENIC	homozygous	113126358
4	79022044	79022045	A	C	13	GENIC	homozygous	113126359
4	79022049	79022050	C	T	12	GENIC	homozygous	113126360
4	79022051	79022052	G	C	12	GENIC	homozygous	113126361
4	79022083	79022084	T	A	13	GENIC	homozygous	113126362
4	79022714	79022715	A	C	27	GENIC	possibly homozygous	113459438
4	79022847	79022848	T	C	28	GENIC	homozygous	113126369
4	79022987	79022988	A	G	20	GENIC	homozygous	113126371
4	79024283	79024284	T	C	18	GENIC	homozygous	113459440
4	79024977	79024978	G	A	26	GENIC	homozygous	113126402
4	79027989	79027990	T	C	19	GENIC	homozygous	112740199
4	79029472	79029473	C	A	28	GENIC	homozygous	112740207
4	79030071	79030072	T	C	8	GENIC	homozygous	112740209
4	79032565	79032566	A	G	27	GENIC	homozygous	112740215
4	79032862	79032863	T	C	19	GENIC	homozygous	112740223
4	79033874	79033875	A	G	22	GENIC	homozygous	112740229
4	79034003	79034004	T	C	23	GENIC	homozygous	112740231
4	79034186	79034187	C	T	24	GENIC	homozygous	113459448
4	79035045	79035046	T	C	21	GENIC	homozygous	112740235
4	79035330	79035331	T	C	27	GENIC	homozygous	112740237
4	79035426	79035427	A	T	24	GENIC	homozygous	112740239
4	79038030	79038031	A	G	21	GENIC	homozygous	113459452
4	79041963	79041964	C	T	20	GENIC	possibly homozygous	113459454