chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	143937632	143937633	G	T	52	GENIC	heterozygous	116396875
7	143942010	143942011	G	A	16	GENIC	heterozygous	116396876
7	143942291	143942292	A	G	27	GENIC	homozygous	116396877
7	143942373	143942374	T	C	35	GENIC	homozygous	116396878
7	143942641	143942642	A	G	30	GENIC	homozygous	116396879
7	143942890	143942891	A	C	34	GENIC	homozygous	115944797
7	143943180	143943181	C	T	43	GENIC	homozygous	116396880
7	143943735	143943736	C	A	8	GENIC	homozygous	116396881
7	143945583	143945584	A	G	26	GENIC	homozygous	115944798
7	143946079	143946080	A	T	36	GENIC	homozygous	115944799
7	143947046	143947047	C	T	15	GENIC	possibly homozygous	116396882
7	143947715	143947716	T	C	22	GENIC	homozygous	116396883
7	143947910	143947911	G	A	30	GENIC	homozygous	116396884
7	143948028	143948029	C	T	31	GENIC	possibly homozygous	116396885
7	143948053	143948054	C	T	30	GENIC	possibly homozygous	116396886
7	143948257	143948258	A	G	19	GENIC	homozygous	116396887
7	143948523	143948524	G	A	34	GENIC	possibly homozygous	116396888
7	143948622	143948623	T	C	28	GENIC	homozygous	116396889
7	143949334	143949335	G	C	31	GENIC	heterozygous	115944800
7	143949351	143949352	T	C	25	GENIC	homozygous	115944801
7	143949918	143949919	C	T	30	GENIC	homozygous	116396890
7	143952424	143952425	T	C	19	GENIC	homozygous	116396891
7	143955614	143955615	T	C	14	GENIC	homozygous	115944802
7	143956062	143956063	G	A	25	GENIC	homozygous	116396892
7	143956510	143956511	C	T	20	GENIC	homozygous	116396893