chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	79919524	79919525	C	G	55	GENIC	homozygous	112132948
3	79925608	79925609	C	G	9	GENIC	homozygous	131635949
3	79926125	79926126	A	G	48	GENIC	homozygous	111634803
3	79926660	79926661	T	C	43	GENIC	homozygous	112132950
3	79927989	79927990	A	G	52	GENIC	homozygous	111634804
3	79928066	79928067	T	A	41	GENIC	homozygous	111634805
3	79928103	79928104	A	G	45	GENIC	homozygous	120110480
3	79928582	79928583	T	C	33	GENIC	homozygous	112132956
3	79928615	79928616	C	T	34	GENIC	homozygous	112132958
3	79928639	79928640	C	T	33	GENIC	homozygous	111634807
3	79924542	79924544	TG		38	GENIC	homozygous	131624133
3	79926934	79926934		T	44	GENIC	homozygous	132585655
3	79928465	79928465		AAACA	42	GENIC	possibly homozygous	127900247
3	79929023	79929024	G	T	52	GENIC	homozygous	112132960
3	79929031	79929032	A	G	48	GENIC	homozygous	111634808
3	79929381	79929382	C	G	51	GENIC	homozygous	111634809
3	79929584	79929585	A	G	47	GENIC	homozygous	111634811
3	79929937	79929938	A	G	53	GENIC	homozygous	111634814
3	79930647	79930648	A	G	32	GENIC	homozygous	111634815
3	79930997	79930998	C	T	34	GENIC	homozygous	112132962
3	79931175	79931176	G	A	45	GENIC	homozygous	112132964
3	79932228	79932229	C	T	47	GENIC	homozygous	111634816
3	79932539	79932540	G	C	29	GENIC	homozygous	111634817
3	79932813	79932814	T		18	GENIC	possibly homozygous	127900249
3	79932828	79932829	G		12	GENIC	homozygous	127900250
3	79932940	79932950	TGTCTCTGTG		20	GENIC	homozygous	127900251
3	79934695	79934696	T	G	49	GENIC	homozygous	111634818
3	79935861	79935862	C	T	40	GENIC	homozygous	111634820
3	79936065	79936066	A	G	53	GENIC	homozygous	111634822
3	79936593	79936594	A	G	35	GENIC	homozygous	111634823
3	79936733	79936734	T	C	38	GENIC	homozygous	111634824
3	79936951	79936952	C	T	34	GENIC	homozygous	111949815
3	79937468	79937469	C	G	54	GENIC	homozygous	111634827