chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	37368853	37368854	A	G	18	GENIC	homozygous	115380842
12	37370041	37370042	G	A	20	GENIC	homozygous	115511214
12	37371070	37371071	G	A	17	GENIC	homozygous	115475603
12	37371467	37371468	C	T	15	GENIC	homozygous	115475605
12	37372383	37372384	T	C	14	GENIC	homozygous	115493827
12	37374844	37374845	A	G	20	GENIC	homozygous	115380850
12	37375060	37375061	C	T	19	GENIC	homozygous	115511215
12	37376312	37376313	G	C	26	GENIC	homozygous	115320306
12	37376857	37376858	C	T	30	GENIC	homozygous	115511216
12	37377190	37377191	T	C	25	GENIC	homozygous	115511217
12	37384618	37384619	C	G	27	GENIC	homozygous	115320310
12	37385385	37385386	A	C	30	GENIC	homozygous	115380856
12	37386324	37386325	T	C	30	GENIC	homozygous	115320312
12	37386371	37386372	T	C	25	GENIC	homozygous	115511218
12	37386645	37386646	C	T	31	GENIC	homozygous	115511219
12	37386821	37386822	C	T	22	GENIC	homozygous	115511220
12	37387201	37387202	T	C	29	GENIC	homozygous	115380860
12	37388042	37388043	C	T	31	GENIC	homozygous	115511221
12	37389149	37389150	A	G	21	GENIC	homozygous	115320316
12	37389552	37389553	C	T	22	GENIC	homozygous	115511222
12	37389967	37389968	T	G	24	GENIC	homozygous	115380866
12	37390001	37390002	G	A	23	GENIC	homozygous	115511223
12	37390056	37390057	A	G	18	GENIC	homozygous	115380868
12	37390087	37390088	C	T	18	GENIC	homozygous	115511224
12	37390182	37390183	C	T	9	GENIC	homozygous	115511225
12	37393618	37393619	C	T	13	GENIC	homozygous	115511226
12	37395108	37395109	A	C	11	GENIC	homozygous	115380874
12	37396046	37396047	T	C	18	GENIC	homozygous	115380878
12	37396056	37396057	T	C	20	GENIC	homozygous	115380880
12	37396308	37396309	G	C	14	GENIC	homozygous	115380882
12	37397137	37397138	A	G	31	GENIC	homozygous	115511228