chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	147825943	147825944	G	A	8	GENIC	homozygous	55780350
5	147826094	147826095	C	T	15	GENIC	homozygous	55780352
5	147826379	147826380	C	A	22	GENIC	possibly homozygous	55780354
5	147826654	147826655	G	A	20	GENIC	homozygous	55780356
5	147827301	147827302	T	-	16	GENIC	homozygous	55780358
5	147827381	147827382	C	T	21	GENIC	possibly homozygous	55780360
5	147827570	147827571	T	A	19	GENIC	homozygous	55780362
5	147827665	147827666	C	T	14	GENIC	homozygous	55780364
5	147828207	147828208	A	C	19	GENIC	heterozygous	55780374
5	147829767	147829768	T	A	15	GENIC	homozygous	55780382
5	147831558	147831563	CACTG	-----	2	GENIC	homozygous	55780400
5	147832977	147832978	C	T	14	GENIC	homozygous	55780404
5	147833655	147833656	G	A	12	GENIC	homozygous	55780406
5	147834162	147834163	T	C	19	GENIC	possibly homozygous	55780408
5	147834395	147834396	A	G	15	GENIC	homozygous	55780410
5	147834545	147834546	T	C	10	GENIC	possibly homozygous	55780412