chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	208769664	208769665	T	C	36	GENIC	homozygous	57066957
4	208770232	208770233	A	-	14	GENIC	homozygous	57066958
4	208775104	208775105	G	A	25	GENIC	homozygous	57607914
4	208770260	208770261	C	A	17	GENIC	homozygous	57607902
4	208770460	208770461	T	A	29	GENIC	homozygous	57607904
4	208770921	208770922	C	CA	39	GENIC	homozygous	57607906
4	208774071	208774072	G	T	35	GENIC	homozygous	57607910
4	208774448	208774449	T	C	31	GENIC	homozygous	57607912
4	208775145	208775146	A	G	26	GENIC	homozygous	57607916
4	208776680	208776681	C	T	13	GENIC	homozygous	57607918
4	208777824	208777825	T	C	42	GENIC	homozygous	57066962
4	208779028	208779029	C	T	35	GENIC	homozygous	57066963
4	208779043	208779044	C	G	35	GENIC	homozygous	57066964
4	208779477	208779485	TTTTTTTT	--------	11	GENIC	heterozygous	57607920
4	208779776	208779779	AAC	---	8	GENIC	homozygous	57066965
4	208779797	208779798	C	CT	3	GENIC	homozygous	57607922
4	208780591	208780592	C	CAT	15	GENIC	heterozygous	57607924
4	208780593	208780594	C	T	15	GENIC	heterozygous	57747433
4	208780595	208780596	C	CACACAG	13	GENIC	homozygous	57066966
4	208780682	208780683	A	AT	13	GENIC	homozygous	57066967
4	208782951	208782952	C	T	6	GENIC	homozygous	57066969
4	208783088	208783089	G	T	14	GENIC	homozygous	57066970
4	208783142	208783143	A	T	18	GENIC	homozygous	57607928
4	208783383	208783384	C	G	23	GENIC	homozygous	57607930
4	208783620	208783621	G	T	27	GENIC	homozygous	57066972
4	208784079	208784080	G	C	27	GENIC	homozygous	57066973
4	208784088	208784089	G	C	25	GENIC	homozygous	57066974