chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	134493078	134493079	A	G	77	GENIC	homozygous	114534528
5	134493079	134493080	A	G	79	GENIC	homozygous	114534530
5	134494890	134494891	G	T	37	GENIC	possibly homozygous	114534532
5	134495795	134495796	G	A	39	GENIC	homozygous	114534536
5	134496303	134496304	A	G	41	GENIC	homozygous	114534538
5	134496374	134496375	C	T	56	GENIC	homozygous	114534540
5	134498638	134498639	C	T	43	GENIC	possibly homozygous	114534542
5	134499806	134499807	C	A	49	GENIC	homozygous	114534544
5	134501999	134502000	C	G	41	GENIC	homozygous	114534546
5	134502253	134502254	C	G	50	GENIC	homozygous	114534548
5	134505045	134505046	C	A	13	GENIC	possibly homozygous	114534550
5	134506309	134506310	T	C	47	GENIC	homozygous	114534552
5	134506310	134506311	G	A	47	GENIC	homozygous	114534554
5	134506795	134506796	G	T	54	GENIC	homozygous	114534556
5	134505781	134505782	A	G	42	GENIC	homozygous	114143995
5	134497244	134497245	C		69	GENIC	homozygous	128241794
5	134497466	134497467	C		48	GENIC	homozygous	128241795
5	134502206	134502210	ACAG		45	GENIC	homozygous	132844212