chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	123209917	123209917		T	46	GENIC	homozygous	127925569
3	123210158	123210158		G	40	GENIC	homozygous	127925570
3	123210666	123210666		GCTGTC	47	GENIC	homozygous	127925571
3	123214018	123214019	T	G	33	GENIC	homozygous	111692086
3	123210663	123210664	A	T	46	GENIC	homozygous	111692080
3	123210480	123210481	G	T	49	GENIC	homozygous	111692078
3	123210509	123210510	A	G	43	GENIC	homozygous	111692079
3	123211679	123211680	T	C	27	GENIC	homozygous	111692081
3	123212764	123212765	C	T	51	GENIC	homozygous	111692082
3	123213093	123213094	G	A	54	GENIC	homozygous	111692083
3	123213309	123213310	C	T	50	GENIC	homozygous	111692084
3	123213588	123213589	T	A	48	GENIC	homozygous	111692085
3	123210667	123210668	G	C	45	GENIC	homozygous	119651444
3	123214554	123214554		ATGCCT	61	GENIC	homozygous	127925572
3	123214646	123214647	C	T	56	GENIC	homozygous	111692087
3	123215525	123215526	A	T	54	GENIC	homozygous	111692088
3	123215919	123215920	A	G	48	GENIC	homozygous	111692089
3	123215941	123215944	CTT		45	GENIC	homozygous	127925573
3	123215945	123215948	TAT		46	GENIC	homozygous	127925574
3	123215950	123215951	A		47	GENIC	homozygous	127925575
3	123215951	123215952	T	G	46	GENIC	homozygous	119651445
3	123216647	123216648	T	C	41	GENIC	homozygous	119801182
3	123216926	123216927	G	A	53	GENIC	homozygous	111692090
3	123217142	123217143	A	G	16	GENIC	homozygous	111692091
3	123217206	123217206		AG	32	GENIC	homozygous	127925576
3	123217390	123217391	C	T	46	GENIC	homozygous	111692092
3	123217471	123217472	G	A	47	GENIC	homozygous	111692093
3	123218338	123218338		CTGCCT	50	GENIC	homozygous	127925577
3	123218376	123218377	T	A	41	GENIC	heterozygous	119651446
3	123218377	123218378	T	A	41	GENIC	heterozygous	132293226
3	123219843	123219857	TCAAACATGGTGTG		52	GENIC	homozygous	127925578
3	123219859	123219866	GGGGCCC		52	GENIC	homozygous	127925579