chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	60780790	60780795	GCTCG		25	GENIC	homozygous	141682657
5	60780824	60780825	A	G	25	GENIC	homozygous	141727800
5	60781216	60781217	G	C	20	GENIC	homozygous	146131338
5	60781586	60781587	A	T	15	GENIC	homozygous	141727801
5	60784878	60784879	G	A	12	GENIC	homozygous	146131339
5	60782150	60782151	T	A	15	GENIC	homozygous	141727802
5	60782340	60782341	T	G	27	GENIC	homozygous	141727803
5	60783318	60783319	A	G	13	GENIC	homozygous	141727805
5	60783677	60783678	C	T	16	GENIC	homozygous	141727806
5	60783834	60783835	C	T	18	GENIC	homozygous	141727807
5	60784784	60784785	A	G	12	GENIC	homozygous	141727809
5	60781464	60781465	C		7	GENIC	homozygous	146120573
5	60783135	60783135		T	21	GENIC	homozygous	137311563
5	60785445	60785446	T	C	17	GENIC	homozygous	141727810
5	60786358	60786359	C	T	20	GENIC	homozygous	146131340
5	60786459	60786459		T	23	GENIC	homozygous	146120574
5	60786638	60786639	T	G	14	GENIC	homozygous	146131341
5	60786639	60786640	C	A	14	GENIC	homozygous	146131342
5	60787539	60787540	C	T	22	GENIC	homozygous	146131343
5	60788568	60788569	A	T	15	GENIC	homozygous	146131344
5	60788014	60788015	C	T	29	GENIC	homozygous	137482127
5	60790159	60790160	A	C	9	GENIC	homozygous	137482129
5	60792123	60792124	T	C	16	GENIC	homozygous	137482132
5	60792551	60792552	T	G	21	GENIC	homozygous	137482133
5	60793229	60793230	T	C	15	GENIC	homozygous	137482134
5	60794213	60794214	G	T	26	GENIC	homozygous	146131345
5	60794742	60794743	C	T	33	GENIC	homozygous	146131346
5	60795230	60795231	C	T	22	GENIC	homozygous	146131347
5	60795864	60795865	C	T	15	GENIC	homozygous	146131348
5	60796889	60796890	A	G	14	GENIC	homozygous	137482136
5	60797214	60797215	A	G	23	GENIC	homozygous	137482137