chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62168855	62168856	T	C	46	GENIC	homozygous	52990235
8	62170191	62170192	G	GTTTGT	18	GENIC	homozygous	52668838
8	62172237	62172238	A	AGCG	3	GENIC	homozygous	53389359
8	62171469	62171470	G	GCC	13	GENIC	homozygous	53700946
8	62172226	62172227	T	TGGG	3	GENIC	homozygous	53389357
8	62172235	62172236	T	TTAGCTCAGTGGTA	3	GENIC	homozygous	53389358
8	62172241	62172242	G	GCCTAGCAAGC	3	GENIC	homozygous	53389360
8	62172281	62172282	A	-	5	GENIC	heterozygous	53700947
8	62173572	62173573	C	T	41	GENIC	homozygous	53700948
8	62174054	62174055	C	T	23	GENIC	homozygous	53273775
8	62174120	62174121	A	G	13	GENIC	homozygous	53273776
8	62174305	62174306	C	T	20	GENIC	homozygous	53700949
8	62174491	62174492	C	T	24	GENIC	homozygous	52990294
8	62174521	62174522	C	T	32	GENIC	homozygous	53700950
8	62175018	62175019	G	C	48	GENIC	homozygous	52990308
8	62175211	62175212	T	C	41	GENIC	homozygous	53273780
8	62175226	62175227	A	G	39	GENIC	homozygous	52990310
8	62175237	62175238	T	TGTGTGCGTGCATGC	6	GENIC	homozygous	53964275
8	62175268	62175269	G	GTGTGTGTGTC	34	GENIC	possibly homozygous	53700951
8	62175417	62175418	A	G	28	GENIC	homozygous	52990313
8	62176229	62176230	T	-	29	GENIC	homozygous	53700952
8	62176233	62176239	TTTGTT	------	29	GENIC	homozygous	53700953
8	62176608	62176610	AA	--	20	GENIC	heterozygous	52990315
8	62176609	62176610	A	-	20	GENIC	heterozygous	52990317
8	62177132	62177133	T	C	63	GENIC	homozygous	53273786