chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	184184339	184184340	A	ATC	13	GENIC	heterozygous	61313321
1	184184394	184184395	C	T	23	GENIC	possibly homozygous	60998679
1	184184740	184184741	C	T	67	GENIC	homozygous	60998680
1	184185044	184185045	G	C	83	GENIC	homozygous	60998681
1	184185799	184185800	G	A	53	GENIC	homozygous	60998682
1	184185935	184185936	T	C	56	GENIC	homozygous	60998683
1	184185938	184185939	T	C	57	GENIC	homozygous	60998684
1	184185966	184185967	T	-	36	GENIC	possibly homozygous	60998685
1	184186294	184186295	G	A	49	GENIC	homozygous	60998686
1	184186366	184186371	GCGCC	-----	17	GENIC	homozygous	60998687
1	184186369	184186374	CCGCC	-----	21	GENIC	homozygous	60998688
1	184186433	184186434	T	C	44	GENIC	possibly homozygous	60998689
1	184186679	184186680	G	A	65	GENIC	possibly homozygous	60998690
1	184187250	184187251	A	ATT	36	GENIC	homozygous	60998691
1	184188059	184188060	C	T	59	GENIC	homozygous	60998692
1	184188545	184188546	G	GT	47	GENIC	possibly homozygous	60998693
1	184188868	184188872	ACAC	----	19	GENIC	possibly homozygous	60998694
1	184188883	184188884	C	T	23	GENIC	heterozygous	60998695
1	184188898	184188899	G	A	32	GENIC	heterozygous	60998696
1	184188909	184188910	G	A	34	GENIC	heterozygous	60998697
1	184188919	184188920	A	G	33	GENIC	heterozygous	60998698