chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	44153355	44153356	C	A	25	GENIC	homozygous	116153208
7	44157413	44157414	G	T	15	GENIC	homozygous	116153210
7	44162427	44162428	C	T	11	GENIC	homozygous	116153212
7	44162872	44162873	A	G	18	GENIC	homozygous	115663004
7	44162897	44162898	G	A	11	GENIC	homozygous	116153214
7	44163966	44163967	T	C	24	GENIC	homozygous	115663006
7	44165165	44165166	A	G	16	GENIC	homozygous	116153216
7	44166953	44166954	C	T	18	GENIC	homozygous	116153220
7	44170370	44170371	C	T	11	GENIC	homozygous	116153222
7	44171050	44171051	C	A	19	GENIC	homozygous	115663031
7	44172391	44172392	T	C	15	GENIC	homozygous	115663041
7	44172911	44172912	C	T	20	GENIC	homozygous	115663044
7	44173623	44173624	T	G	28	GENIC	homozygous	115663046
7	44174280	44174281	T	C	7	GENIC	homozygous	116153224
7	44174559	44174560	T	C	13	GENIC	homozygous	115663054
7	44174659	44174660	T	A	14	GENIC	homozygous	116153226
7	44174726	44174727	T	G	21	GENIC	homozygous	116153228
7	44175000	44175001	C	G	22	GENIC	homozygous	116023922
7	44176384	44176385	A	G	18	GENIC	homozygous	115663066
7	44176597	44176598	T	C	19	GENIC	homozygous	116153230
7	44176648	44176649	A	G	11	GENIC	homozygous	115663067
7	44176899	44176900	T	C	26	GENIC	homozygous	115663068
7	44177694	44177695	T	C	19	GENIC	homozygous	115663070
7	44176661	44176662	A	G	14	GENIC	homozygous	116288136
7	44176660	44176661	G	C	12	GENIC	homozygous	118307450