chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	81208413	81208414	T	C	24	GENIC	homozygous	112748239
4	81209606	81209607	T	C	31	GENIC	homozygous	113461194
4	81210744	81210745	C	T	20	GENIC	possibly homozygous	113461196
4	81212090	81212091	A	G	18	GENIC	homozygous	113128100
4	81213132	81213133	A	T	19	GENIC	homozygous	112748243
4	81215251	81215252	C	T	15	GENIC	homozygous	113461198
4	81216563	81216564	A	G	25	GENIC	homozygous	112748251
4	81217264	81217265	C	T	23	GENIC	homozygous	113461200
4	81217775	81217776	T	C	21	GENIC	homozygous	113461202
4	81218358	81218359	A	T	31	GENIC	homozygous	113461204
4	81219204	81219205	T	C	13	GENIC	homozygous	112748255
4	81220000	81220001	A	G	28	GENIC	homozygous	112748259
4	81220089	81220090	C	T	30	GENIC	homozygous	113461208
4	81223921	81223922	A	G	25	GENIC	homozygous	112748271
4	81225013	81225014	G	A	30	GENIC	homozygous	113461216
4	81225323	81225324	C	T	21	GENIC	homozygous	113128104
4	81225996	81225997	T	A	27	GENIC	homozygous	113128106
4	81226951	81226952	G	A	16	GENIC	homozygous	113461218
4	81230543	81230544	G	A	27	GENIC	homozygous	113461220
4	81223680	81223681	A	G	18	GENIC	homozygous	119307535
4	81223681	81223682	G	A	17	GENIC	homozygous	119307537