chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	92029471	92029472	G	T	19	GENIC	possibly homozygous	54022261
7	92029963	92029964	C	T	21	GENIC	possibly homozygous	54208558
7	92030703	92030704	G	GT	4	GENIC	homozygous	54022268
7	92031574	92031575	A	AT	14	GENIC	possibly homozygous	54208559
7	92031691	92031692	G	A	16	GENIC	homozygous	54208560
7	92031771	92031772	G	A	12	GENIC	heterozygous	54208561
7	92031934	92031935	T	C	2	GENIC	heterozygous	54022273
7	92032184	92032185	G	A	17	GENIC	homozygous	54208562
7	92033062	92033063	C	A	19	GENIC	possibly homozygous	54208563
7	92033260	92033261	C	T	7	GENIC	possibly homozygous	54208564
7	92033441	92033442	G	C	16	GENIC	homozygous	54022276
7	92033680	92033681	C	T	18	GENIC	homozygous	54022278
7	92030824	92030946	GGAAATTTTTCTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCA	--------------------------------------------------------------------------------------------------------------------------	6	GENIC	heterozygous	54912057