chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	7596246	7596250	TGTG	----	19	GENIC	possibly homozygous	45841117
20	7597103	7597104	C	CA	37	GENIC	homozygous	45413969
20	7597867	7597868	A	G	26	GENIC	homozygous	45413972
20	7600176	7600177	C	T	27	GENIC	possibly homozygous	45973354
20	7601748	7601777	TGGGCTGTGGCGGCCGTCTACTAACTGCG	-----------------------------	12	GENIC	homozygous	45413977
20	7602005	7602010	GACAC	-----	1	GENIC	homozygous	45413978
20	7602147	7602153	GCGGTG	------	7	GENIC	homozygous	45841119
20	7602456	7602457	G	A	23	GENIC	homozygous	45973355
20	7603609	7603610	T	C	28	GENIC	homozygous	45413982
20	7604275	7604276	A	C	42	GENIC	homozygous	45413986
20	7604933	7604934	T	C	31	GENIC	homozygous	45973356
20	7606561	7606562	T	TCGCAGAGTGGA	27	GENIC	homozygous	45973357
20	7608061	7608062	T	G	37	GENIC	homozygous	45973358
20	7609610	7609611	T	-	14	GENIC	homozygous	45973359
20	7611101	7611102	G	A	22	GENIC	homozygous	45973360
20	7612759	7612760	G	A	25	GENIC	homozygous	45414015
20	7616784	7616785	C	G	23	GENIC	homozygous	45414019
20	7617455	7617456	A	G	30	GENIC	homozygous	45414021
20	7621197	7621198	A	G	30	GENIC	homozygous	45414026