chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3971347	3971348	T	G	56	GENIC	homozygous	130027202
20	3971517	3971518	A	T	48	GENIC	homozygous	130027203
20	3971523	3971524	C	G	47	GENIC	homozygous	130027204
20	3971848	3971849	T	C	46	GENIC	homozygous	130027205
20	3971986	3971987	G	C	58	GENIC	possibly homozygous	130027206
20	3972117	3972118	T	C	44	GENIC	homozygous	130027207
20	3972294	3972295	C	T	49	GENIC	homozygous	130027208
20	3972415	3972416	A	G	53	GENIC	possibly homozygous	130027209
20	3972754	3972755	T	C	43	GENIC	homozygous	130027210
20	3973034	3973035	C	T	45	GENIC	homozygous	130027211
20	3973782	3973785	CTT		51	GENIC	homozygous	129978753
20	3973800	3973801	G	C	57	GENIC	homozygous	130027212
20	3974134	3974135	T	C	49	GENIC	homozygous	130027213
20	3974150	3974151	A	G	51	GENIC	homozygous	130027214
20	3974199	3974200	G	T	55	GENIC	homozygous	130027215
20	3974963	3974965	TA		48	GENIC	homozygous	129978754
20	3975066	3975067	G	T	50	GENIC	homozygous	130027216
20	3975288	3975289	A	G	55	GENIC	homozygous	130027217
20	3975525	3975526	G	A	59	GENIC	homozygous	130027218
20	3975947	3975948	C	T	56	GENIC	homozygous	130027219
20	3976284	3976285	C	T	63	GENIC	homozygous	130027220
20	3976462	3976463	C	G	51	GENIC	homozygous	130027221