chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11254390	11254391	C	T	31	GENIC	homozygous	53787853
7	11254526	11254527	G	T	33	GENIC	homozygous	53787855
7	11254786	11254787	T	C	37	GENIC	homozygous	53787858
7	11255117	11255118	T	C	28	GENIC	possibly homozygous	53787861
7	11256317	11256318	G	A	35	GENIC	possibly homozygous	54181342
7	11256345	11256346	G	A	38	GENIC	homozygous	54181343
7	11257231	11257232	C	T	32	GENIC	possibly homozygous	54181344
7	11257547	11257548	T	C	35	GENIC	homozygous	53787864
7	11257684	11257685	C	A	36	GENIC	homozygous	53787866
7	11257775	11257776	T	TTGAA	39	GENIC	homozygous	53787868
7	11257902	11257903	T	C	34	GENIC	homozygous	54181345
7	11258228	11258229	A	G	31	GENIC	homozygous	53787872
7	11258410	11258411	C	T	43	GENIC	homozygous	53787874
7	11258455	11258456	C	T	40	GENIC	homozygous	54181346
7	11258722	11258723	T	C	39	GENIC	homozygous	53787875
7	11259091	11259092	C	T	41	INTERGENIC	homozygous	54181347