chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	130556123	130556124	A	G	18	GENIC	homozygous	115890580
7	130556165	130556166	C	T	9	GENIC	homozygous	115890582
7	130556669	130556670	A	G	21	GENIC	homozygous	115890584
7	130556712	130556713	G	T	25	GENIC	homozygous	115890586
7	130556727	130556728	A	T	28	GENIC	homozygous	115890588
7	130556738	130556739	A	G	30	GENIC	homozygous	115890590
7	130557064	130557065	T	C	27	GENIC	homozygous	115890592
7	130557291	130557292	G	A	20	GENIC	homozygous	115890594
7	130557836	130557837	C	T	12	GENIC	homozygous	115890596
7	130558518	130558519	G	A	35	GENIC	homozygous	115890598
7	130558657	130558658	T	C	23	GENIC	homozygous	115890600
7	130558747	130558748	G	T	25	GENIC	homozygous	115890602
7	130558847	130558848	T	C	26	GENIC	homozygous	115890604
7	130559154	130559155	T	C	9	GENIC	homozygous	115890606
7	130559962	130559963	A	G	23	GENIC	homozygous	115890608
7	130559993	130559994	C	A	21	GENIC	homozygous	115890609
7	130560530	130560531	A	G	22	GENIC	homozygous	115890611
7	130560735	130560736	G	A	22	GENIC	homozygous	115890613
7	130561146	130561147	A	G	26	GENIC	homozygous	115890615
7	130561201	130561202	C	T	33	GENIC	homozygous	115890617
7	130561298	130561299	G	A	17	GENIC	homozygous	115890619
7	130561671	130561672	T	C	24	GENIC	homozygous	115890621
7	130561781	130561782	C	T	16	GENIC	homozygous	115890623
7	130561970	130561971	T	C	19	GENIC	homozygous	115890625
7	130563831	130563832	G	C	29	GENIC	homozygous	115890627
7	130564355	130564356	A	T	15	GENIC	homozygous	115890631
7	130564596	130564597	T	C	8	GENIC	homozygous	115890633
7	130564617	130564618	T	C	7	GENIC	homozygous	115890635