chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	3733867	3733868	A	G	28	GENIC	homozygous	66599605
12	3747414	3747415	C	T	36	GENIC	possibly homozygous	66599607
12	3748209	3748210	C	G	34	GENIC	homozygous	66599608
12	3748423	3748424	C	A	26	GENIC	homozygous	66599609
12	3750713	3750715	T	AT	5	GENIC		67654330
12	3750733	3750734	A	T	19	GENIC	heterozygous	66599610
12	3755052	3755053	C	A	31	GENIC	possibly homozygous	66599612
12	3755695	3755696	C	T	20	GENIC	homozygous	66599613
12	3757251	3757252	G	T	36	GENIC	homozygous	66599614
12	3761302	3761303	A	G	16	GENIC	homozygous	66599616
12	3762286	3762287	A	G	24	GENIC	possibly homozygous	66599617
12	3764099	3764100	G	A	15	GENIC	homozygous	66599621
12	3764106	3764107	C	T	14	GENIC	homozygous	66599622
12	3764255	3764256	T	C	28	GENIC	homozygous	66599623
12	3769038	3769039	G	A	18	GENIC	homozygous	66599625
12	3769134	3769135	G	C	30	GENIC	homozygous	66599626
12	3769184	3769185	C	G	12	GENIC	homozygous	66599627
12	3769453	3769454	C	G	23	GENIC	homozygous	66599628