chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	152495708	152495709	A	G	16	GENIC	homozygous	114543620
5	152495841	152495842	T	A	22	GENIC	homozygous	114543622
5	152497704	152497707	AAC		9	GENIC	homozygous	131391318
5	152498267	152498268	A	G	19	GENIC	homozygous	114543624
5	152503573	152503574	G	A	25	GENIC	homozygous	114543632
5	152503361	152503362	A	G	13	GENIC	homozygous	114543626
5	152503376	152503377	T	C	14	GENIC	homozygous	114543628
5	152503529	152503530	T	C	25	GENIC	homozygous	114543630
5	152504221	152504222	T	C	28	GENIC	homozygous	114543634
5	152504269	152504270	A	G	35	GENIC	homozygous	114543636
5	152504511	152504513	AT		17	GENIC	possibly homozygous	131391319
5	152504526	152504562	CTCTCTCTCTCTCTCTCTCTCTCTCCCTCTCCCTCC		16	GENIC	heterozygous	131391320
5	152504584	152504585	T	C	16	GENIC	possibly homozygous	114543640
5	152504745	152504746	A	T	24	GENIC	homozygous	114543642
5	152505127	152505128	A	G	25	GENIC	homozygous	114543644
5	152506524	152506525	G	A	21	GENIC	homozygous	114543646
5	152506735	152506736	T	C	21	GENIC	homozygous	114543648
5	152507198	152507199	G	A	17	GENIC	homozygous	114543650
5	152507229	152507230	A	G	16	GENIC	homozygous	114543652
5	152507348	152507349	T	C	20	GENIC	homozygous	114543654
5	152507692	152507692		GG	10	GENIC	homozygous	131391321