chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	54951656	54951657	T	C	36	GENIC	homozygous	109762925
2	54953466	54953467	G	A	28	GENIC	homozygous	110530985
2	54954319	54954320	T	C	35	GENIC	homozygous	109762933
2	54954683	54954684	C	T	43	GENIC	homozygous	110530987
2	54954997	54954998	A	G	37	GENIC	homozygous	109762935
2	54955053	54955054	T	C	33	GENIC	homozygous	109762937
2	54955606	54955607	T	C	27	GENIC	homozygous	109762938
2	54955811	54955812	A	G	27	GENIC	homozygous	109762942
2	54956730	54956731	C	T	29	GENIC	homozygous	110530989
2	54958071	54958072	C	T	25	GENIC	homozygous	110530991
2	54958355	54958356	T	G	27	GENIC	homozygous	110530993
2	54958835	54958836	A	G	22	GENIC	homozygous	109762956
2	54958896	54958897	A	G	43	GENIC	homozygous	109762958
2	54960374	54960375	T	G	26	GENIC	homozygous	109762964
2	54961481	54961482	T	G	18	GENIC	homozygous	109762970
2	54961817	54961818	T	C	9	GENIC	homozygous	109762972
2	54962435	54962436	T	A	19	GENIC	homozygous	109762980
2	54964196	54964197	C	T	8	GENIC	homozygous	110530995
2	54964809	54964810	G	T	13	GENIC	homozygous	110530996
2	54965371	54965372	C	A	21	GENIC	homozygous	109762984
2	54965425	54965426	A	G	29	GENIC	homozygous	110530998
2	54965538	54965539	G	A	21	GENIC	homozygous	110530999