chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	141041132	141041133	C	T	56	GENIC	homozygous	115939685
7	141041404	141041405	A		28	GENIC	possibly homozygous	128529393
7	141041587	141041588	A	T	53	GENIC	homozygous	115939686
7	141043436	141043437	G	A	30	GENIC	homozygous	115939687
7	141044200	141044211	AAAAAGAAAAG		38	GENIC	possibly homozygous	128529394
7	141044243	141044244	G	A	42	GENIC	homozygous	115939688
7	141045765	141045765		A	48	GENIC	possibly homozygous	128529395
7	141052572	141052573	C		16	GENIC	homozygous	128529396
7	141053521	141053522	C	G	36	GENIC	homozygous	115939690
7	141054282	141054283	A	G	91	GENIC	homozygous	115939691
7	141056273	141056274	C	T	63	GENIC	homozygous	115939692
7	141042385	141042385		A	38	GENIC	heterozygous	132112853
7	141049202	141049202		GGTTC	2	GENIC	homozygous	132478907
7	141049206	141049206		TTTC	2	GENIC	homozygous	132478908
7	141049208	141049208		AGCTGGGGACCGAACCCAGGGCCTTGCGCTTGCTAGGCCAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCTCTTT	2	GENIC	homozygous	132478909
7	141060510	141060511	A	G	49	GENIC	homozygous	115939693
7	141061219	141061219		C	37	GENIC	possibly homozygous	128529397
7	141062481	141062484	TCA		39	GENIC	homozygous	128529398
7	141063700	141063700		TGTT	53	GENIC	homozygous	128529399
7	141063969	141064011	TTTCCTTTTAAAAAAACGTTATCGTCAGCAAAACTAATGTTA		33	GENIC	homozygous	128529400
7	141066029	141066030	T	C	68	GENIC	homozygous	115939695
7	141066780	141066781	C	T	63	GENIC	homozygous	115939696
7	141068996	141068997	G	A	72	GENIC	homozygous	115939697
7	141069363	141069363		TTTTTTAAATTGTCAACCGTTGTTACTGATTGGTCTCC	57	GENIC	homozygous	128529401
7	141069637	141069637		G	64	GENIC	homozygous	128529402