chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	54491273	54491274	T		12	GENIC	homozygous	128341609
6	54491288	54491289	T		10	GENIC	homozygous	128341610
6	54499455	54499456	A	C	17	GENIC	heterozygous	115059878
6	54519533	54519533		AAATGG	16	GENIC	homozygous	128341624
6	54538059	54538059		TGCTTGCT	9	GENIC	homozygous	128341637
6	54549362	54549363	T	C	7	GENIC	homozygous	114804470
6	54549369	54549370	G		6	GENIC	homozygous	128341638
6	54549444	54549445	C		5	GENIC	homozygous	128341639
6	54585670	54585671	G	C	9	GENIC	homozygous	114804521
6	54585682	54585683	A	C	8	GENIC	homozygous	114804522
6	54585725	54585726	A	C	9	GENIC	homozygous	118627905
6	54585729	54585730	G	C	10	GENIC	homozygous	118627906
6	54585734	54585735	G	T	10	GENIC	homozygous	118627907
6	54585735	54585736	A	T	10	GENIC	homozygous	118627908
6	54585737	54585738	A	C	10	GENIC	homozygous	118627909
6	54585738	54585739	A	T	10	GENIC	homozygous	118627910
6	54585739	54585740	G	T	10	GENIC	homozygous	118627911
6	54585745	54585746	C	T	12	GENIC	homozygous	118627912
6	54585749	54585750	C	T	12	GENIC	homozygous	118627913
6	54585760	54585761	A	C	14	GENIC	homozygous	118627914
6	54585761	54585762	G	T	14	GENIC	homozygous	118627915
6	54585775	54585777	AG		13	GENIC	homozygous	130326757
6	54569633	54569778	CTCCCTCCCTCCCTCCCTTTGGACCGGCGGCCGGCTGGGGGGGCGGTTCCTCTTAAGGTCTGCAGCAGGAATGGGGCGGGGGGTAGAGAGAATGGGTGTGAGACGGCAAGAAGGAAGGAAGGGGGGAGCGGGCGGAGGACGGACG		8	GENIC	homozygous	130556383
6	54585752	54585753	A	C	12	GENIC	homozygous	130334213
6	54585753	54585754	G	T	12	GENIC	homozygous	130334214
6	54585757	54585758	A	T	13	GENIC	homozygous	130334215
6	54585765	54585767	AG		14	GENIC	homozygous	130326755
6	54585768	54585771	AAG		14	GENIC	homozygous	130326756