chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	122665391	122665392	T	C	55	GENIC	homozygous	137607815
5	122665621	122665621		AAAC	42	GENIC	homozygous	146122412
5	122668191	122668192	G	A	30	GENIC	homozygous	137607823
5	122668509	122668510	T	G	33	GENIC	homozygous	137607825
5	122669199	122669200	G	A	41	GENIC	homozygous	146138796
5	122667220	122667221	T	A	46	GENIC	homozygous	146138793
5	122667983	122667984	C	T	43	GENIC	homozygous	146138794
5	122668932	122668933	G	A	52	GENIC	homozygous	146138795
5	122669215	122669216	C	T	44	GENIC	homozygous	146138797
5	122669436	122669437	G	A	49	GENIC	homozygous	146138798
5	122670468	122670469	G	A	42	GENIC	homozygous	146138799
5	122670720	122670721	A	T	39	GENIC	possibly homozygous	146138800
5	122671236	122671237	C	T	1	GENIC	homozygous	137607830
5	122671357	122671358	G	A	22	GENIC	homozygous	146138801
5	122671564	122671565	A		19	GENIC	homozygous	146122413
5	122671592	122671593	T	A	22	GENIC	homozygous	146138802
5	122671863	122671864	A	G	39	GENIC	homozygous	137607832
5	122676735	122676786	TCCTCCCCTTTCTCCTTTTCCTCCTCTTTCTCCTTTTCCTCCTCTTCTTCC		4	GENIC	homozygous	146122414
5	122680183	122680184	T	G	31	GENIC	homozygous	146138803
5	122680702	122680703	C	T	48	GENIC	homozygous	146138804
5	122680708	122680709	C	T	47	GENIC	homozygous	146138805
5	122671173	122671173		GTAC	5	GENIC	homozygous	147795251
5	122671564	122671565	A	T	19	GENIC	heterozygous	154319241
5	122676692	122676693	T	C	11	GENIC	homozygous	154319243
5	122676692	122676693	T		11	GENIC	heterozygous	403156019