chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	144015423	144015424	C	T	22	GENIC	homozygous	115944875
7	144019000	144019001	A	G	22	GENIC	homozygous	115944876
7	144022604	144022605	G	A	29	GENIC	homozygous	116100885
7	144023336	144023337	A	G	9	GENIC	homozygous	115944879
7	144023893	144023894	C	A	8	GENIC	homozygous	118261193
7	144024517	144024518	C	T	10	GENIC	homozygous	115944880
7	144025133	144025134	C	T	26	GENIC	homozygous	115944881
7	144027657	144027658	C	T	18	GENIC	homozygous	115944882
7	144028379	144028380	G	A	22	GENIC	homozygous	115944884
7	144029965	144029966	T	C	26	GENIC	homozygous	115944885
7	144031371	144031372	C	A	22	GENIC	homozygous	115944886
7	144031834	144031835	A	C	19	GENIC	homozygous	115944887
7	144032902	144032903	A	G	21	GENIC	homozygous	115944889
7	144034163	144034164	G	C	20	GENIC	homozygous	115944890
7	144034238	144034239	T	G	29	GENIC	homozygous	115944891
7	144034422	144034423	C	A	26	GENIC	homozygous	115944892
7	144035801	144035802	G	A	29	GENIC	homozygous	115944893
7	144036250	144036251	G	A	26	GENIC	homozygous	115944894
7	144036284	144036285	G	A	30	GENIC	homozygous	115944895
7	144037788	144037789	T	C	28	GENIC	homozygous	115944896
7	144038076	144038077	T	G	25	GENIC	homozygous	115944897
7	144038077	144038078	G	A	25	GENIC	homozygous	116305509
7	144041713	144041714	G	A	28	GENIC	possibly homozygous	115944898
7	144044395	144044396	A	T	31	GENIC	homozygous	115944899