chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	70510011	70510012	C	T	70	GENIC	homozygous	143091168
4	70511263	70511264	A		13	GENIC	homozygous	403102991
4	70511263	70511264	A	G	13	GENIC	heterozygous	403102992
4	70513317	70513318	C	G	41	GENIC	homozygous	137079398
4	70514240	70514241	G	A	66	GENIC	homozygous	143091169
4	70514413	70514414	G	T	59	GENIC	possibly homozygous	143091170
4	70514912	70514913	C	T	51	GENIC	homozygous	137079400
4	70516446	70516447	C	T	63	GENIC	homozygous	137079404
4	70516294	70516295	G	A	57	GENIC	homozygous	137079403
4	70517583	70517584	T	C	73	GENIC	homozygous	137079406
4	70517754	70517755	C	A	48	GENIC	homozygous	137079407
4	70518988	70518989	A		50	GENIC	heterozygous	145440927
4	70518988	70518989	A	T	50	GENIC	homozygous	154183579
4	70521526	70521527	T	C	73	GENIC	homozygous	143091171
4	70522168	70522168		A	77	GENIC	possibly homozygous	143050460
4	70522185	70522191	CGATCA		71	GENIC	possibly homozygous	143050461
4	70518318	70518323	CAGTT		58	GENIC	homozygous	143050458
4	70521484	70521485	G		71	GENIC	homozygous	143050459
4	70522255	70522256	T	C	78	GENIC	homozygous	143091172
4	70522290	70522291	G	A	82	GENIC	homozygous	143091173
4	70522329	70522330	A	G	73	GENIC	homozygous	143091174
4	70522356	70522357	G	A	72	GENIC	homozygous	143091175
4	70522552	70522553	T	C	87	GENIC	possibly homozygous	143091176
4	70522826	70522827	A	G	69	GENIC	homozygous	143091177