chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	135841136	135841137	C	T	38	GENIC	homozygous	115920630
7	135841142	135841143	C	T	40	GENIC	homozygous	115920632
7	135841167	135841168	C	T	48	GENIC	homozygous	115920634
7	135841216	135841217	C	G	40	GENIC	homozygous	115920636
7	135841238	135841239	C	T	39	GENIC	homozygous	115920638
7	135841492	135841493	C	T	32	GENIC	homozygous	115920640
7	135842079	135842080	G	A	28	GENIC	homozygous	115920642
7	135842611	135842612	C	T	29	GENIC	homozygous	115920644
7	135843715	135843716	T	C	32	GENIC	homozygous	115920650
7	135843759	135843760	C	T	39	GENIC	heterozygous	118399178
7	135844589	135844590	C	T	28	GENIC	homozygous	115920652
7	135844630	135844631	T	C	34	GENIC	homozygous	115920654
7	135846328	135846329	T	A	24	GENIC	homozygous	115920656
7	135847629	135847630	T	C	29	GENIC	homozygous	115920658
7	135848410	135848411	C	A	12	GENIC	heterozygous	116092207
7	135849410	135849411	T	G	26	GENIC	homozygous	115920662
7	135849614	135849615	C	T	34	GENIC	homozygous	115920664