chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	124449790	124449791	C	T	22	GENIC	homozygous	54093681
7	124449817	124449818	G	-	20	GENIC	homozygous	54093683
7	124450917	124450918	A	G	17	GENIC	homozygous	54093685
7	124451217	124451218	C	T	13	GENIC	homozygous	54093687
7	124451629	124451630	C	CA	31	GENIC	homozygous	54093689
7	124452089	124452090	G	A	19	GENIC	homozygous	54093691
7	124452604	124452605	A	G	31	GENIC	homozygous	54093693
7	124452876	124452877	G	C	8	GENIC	homozygous	54093695
7	124452911	124452912	G	GAA	11	GENIC	heterozygous	54093697
7	124452911	124452912	G	GA	11	GENIC	heterozygous	54921585
7	124453174	124453175	C	-	14	GENIC	homozygous	54093699
7	124453417	124453418	C	-	4	GENIC	homozygous	54093701
7	124453482	124453483	C	-	4	GENIC	homozygous	54093703
7	124453538	124453539	T	C	11	GENIC	homozygous	54093705
7	124453679	124453681	GT	--	12	GENIC	homozygous	54093707
7	124453682	124453683	C	CA	12	GENIC	homozygous	54093709
7	124453684	124453685	G	T	11	GENIC	homozygous	54093711
7	124453738	124453739	A	G	9	GENIC	homozygous	54093713
7	124453766	124453767	C	T	12	GENIC	homozygous	54093715
7	124454208	124454209	A	G	19	GENIC	homozygous	54093717
7	124454297	124454298	C	T	14	GENIC	homozygous	54093719
7	124454320	124454321	G	GA	13	GENIC	homozygous	54093721
7	124454581	124454582	C	G	26	GENIC	homozygous	54093723
7	124454974	124454975	T	A	23	GENIC	homozygous	54093725
7	124455581	124455582	C	T	21	GENIC	homozygous	54093735
7	124455672	124455673	T	-	40	GENIC	homozygous	54093737
7	124455899	124455902	TTT	---	35	GENIC	homozygous	54093739
7	124458367	124458368	A	T	23	GENIC	homozygous	54093747
7	124456166	124456167	C	CGTGTCCGTGTGTGTGTGTGT	11	GENIC	homozygous	55003754