chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	54238969	54238970	C	T	18	GENIC	homozygous	53926860
7	54240666	54240667	T	C	12	GENIC	homozygous	53926861
7	54243359	54243360	G	A	19	GENIC	possibly homozygous	53926863
7	54244506	54244507	T	A	21	GENIC	homozygous	53926864
7	54245075	54245076	C	T	19	GENIC	homozygous	53926865
7	54246676	54246680	TTTC	----	4	GENIC	homozygous	53926866
7	54246685	54246686	G	A	4	GENIC	homozygous	53926867
7	54247212	54247213	T	C	25	GENIC	possibly homozygous	53926868
7	54248465	54248466	C	A	13	GENIC	homozygous	53926869
7	54248837	54248838	G	A	19	GENIC	homozygous	53926870
7	54249464	54249465	A	G	25	GENIC	homozygous	53926871
7	54249907	54249911	TGTT	----	10	GENIC	homozygous	53926872
7	54252028	54252029	A	AGGTCT	1	GENIC	homozygous	54976484
7	54254991	54254992	C	CT	8	GENIC	heterozygous	53926875
7	54255266	54255267	C	T	21	GENIC	possibly homozygous	53926876
7	54255285	54255286	T	C	16	GENIC	homozygous	53926877
7	54256818	54256819	C	T	19	GENIC	possibly homozygous	53926878
7	54256850	54256851	T	G	23	GENIC	possibly homozygous	53926879
7	54258910	54258911	A	G	14	GENIC	homozygous	53926882
7	54259252	54259253	G	A	23	GENIC	possibly homozygous	53926883
7	54259529	54259530	A	AT	3	GENIC	homozygous	53926884
7	54259888	54259889	C	T	18	GENIC	homozygous	53926885
7	54259970	54259971	T	G	14	GENIC	possibly homozygous	53926886
7	54261477	54261479	GT	--	22	GENIC	homozygous	53926888
7	54261861	54261862	G	GT	5	GENIC	heterozygous	53926889