chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	208769664	208769665	T	C	21	GENIC	homozygous	57066957
4	208770232	208770233	A	-	19	GENIC	homozygous	57066958
4	208770260	208770261	C	A	17	GENIC	homozygous	57607902
4	208770460	208770461	T	A	18	GENIC	homozygous	57607904
4	208770593	208770599	ACACAC	------	5	GENIC	homozygous	58369289
4	208770921	208770922	C	CA	46	GENIC	homozygous	57607906
4	208774071	208774072	G	T	22	GENIC	homozygous	57607910
4	208774448	208774449	T	C	18	GENIC	homozygous	57607912
4	208775104	208775105	G	A	19	GENIC	homozygous	57607914
4	208775145	208775146	A	G	24	GENIC	homozygous	57607916
4	208776680	208776681	C	T	19	GENIC	homozygous	57607918
4	208777824	208777825	T	C	25	GENIC	homozygous	57066962
4	208779028	208779029	C	T	23	GENIC	homozygous	57066963
4	208779043	208779044	C	G	21	GENIC	homozygous	57066964
4	208779477	208779485	TTTTTTTT	--------	13	GENIC	heterozygous	57607920
4	208779776	208779779	AAC	---	11	GENIC	homozygous	57066965
4	208779797	208779798	C	CT	7	GENIC	heterozygous	57607922
4	208779797	208779798	C	CTT	7	GENIC	heterozygous	58369291
4	208780591	208780592	C	CAT	12	GENIC	possibly homozygous	57607924
4	208780595	208780596	C	CACACAG	12	GENIC	possibly homozygous	57066966
4	208780595	208780596	C	CACAG	12	GENIC	heterozygous	58369293
4	208780682	208780683	A	AT	17	GENIC	homozygous	57066967
4	208782951	208782952	C	T	20	GENIC	homozygous	57066969
4	208783142	208783143	A	T	28	GENIC	homozygous	57607928
4	208783383	208783384	C	G	34	GENIC	homozygous	57607930
4	208783620	208783621	G	T	16	GENIC	homozygous	57066972
4	208784079	208784080	G	C	22	GENIC	homozygous	57066973
4	208784088	208784089	G	C	22	GENIC	homozygous	57066974