chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	92029028	92029029	T	C	36	GENIC	homozygous	54022258
7	92029133	92029134	G	C	27	GENIC	homozygous	54022259
7	92029171	92029172	T	C	28	GENIC	homozygous	54022260
7	92029471	92029472	G	T	26	GENIC	homozygous	54022261
7	92029476	92029477	T	A	30	GENIC	possibly homozygous	54022262
7	92029858	92029859	C	T	21	GENIC	homozygous	54022263
7	92030172	92030173	G	GATTGATTT	4	GENIC	homozygous	55084008
7	92030500	92030501	C	T	21	GENIC	homozygous	54022267
7	92030703	92030704	G	GT	26	GENIC	homozygous	54022268
7	92030824	92030946	GGAAATTTTTCTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCA	--------------------------------------------------------------------------------------------------------------------------	25	GENIC	homozygous	54912057
7	92031176	92031177	C	T	26	GENIC	possibly homozygous	54022269
7	92031283	92031284	T	TGAGGTAATCCAGTA	28	GENIC	homozygous	54022270
7	92031715	92031716	G	T	21	GENIC	homozygous	54022271
7	92031916	92031917	A	-	10	GENIC	homozygous	54022272
7	92031934	92031935	T	C	16	GENIC	homozygous	54022273
7	92032190	92032191	C	T	17	GENIC	homozygous	54798418
7	92032389	92032390	A	C	21	GENIC	homozygous	54022274