chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	20760885	20760886	C	CTTCA	9	GENIC	homozygous	45469530
20	20760960	20760961	A	G	9	GENIC	heterozygous	45469531
20	20763552	20763553	C	CT	23	GENIC	heterozygous	45469536
20	20764728	20764729	C	-	9	GENIC	possibly homozygous	45469537
20	20765522	20765523	G	A	18	GENIC	homozygous	45469538
20	20765771	20765772	C	T	28	GENIC	possibly homozygous	45469539
20	20767948	20767949	G	A	4	GENIC	homozygous	45469545
20	20768202	20768203	G	-	1	GENIC	homozygous	45469548
20	20768530	20768531	C	T	14	GENIC	possibly homozygous	45469549
20	20769060	20769061	C	T	14	GENIC	homozygous	45469550
20	20769160	20769161	A	G	4	GENIC	homozygous	45469551
20	20769456	20769457	G	A	7	GENIC	heterozygous	45469552
20	20770219	20770220	T	C	26	GENIC	possibly homozygous	45469553
20	20770418	20770422	TCTT	----	3	GENIC	homozygous	45469554
20	20770965	20770966	C	T	18	GENIC	possibly homozygous	45469555
20	20771950	20771951	T	C	25	GENIC	possibly homozygous	45469556
20	20772106	20772107	G	A	19	GENIC	homozygous	45469557
20	20772129	20772130	T	C	16	GENIC	homozygous	45469558