chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	129745152	129745153	C	T	26	GENIC	possibly homozygous	54109535
7	129745635	129745636	A	G	14	GENIC	possibly homozygous	54109536
7	129746108	129746109	G	A	12	GENIC	heterozygous	54109538
7	129747543	129747545	AA	--	2	GENIC	homozygous	54109541
7	129751958	129751959	A	G	14	GENIC	possibly homozygous	54109546
7	129752060	129752182	CTGGTGTCCAGTTTTTTTTTTTTTTTTTTTTTTTTTGGGTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAACCCCCAACCC	--------------------------------------------------------------------------------------------------------------------------	20	GENIC	heterozygous	54922317
7	129752657	129752658	C	T	26	GENIC	homozygous	54109549
7	129753323	129753324	T	C	25	GENIC	possibly homozygous	54109550
7	129753758	129753764	TCCCTG	------	9	GENIC	homozygous	54109551