chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	10203343	10203344	A	G	9	GENIC	heterozygous	50276867
12	10228273	10228274	G	A	27	GENIC	heterozygous	51088167
12	10240071	10240072	C	T	24	GENIC	heterozygous	50042642
12	10240129	10240130	A	G	22	GENIC	heterozygous	51088183
12	10240140	10240141	T	C	21	GENIC	heterozygous	50042644
12	10334932	10334933	A	G	18	GENIC	heterozygous	50044164
12	10335026	10335027	G	A	22	GENIC	heterozygous	50044166
12	10335048	10335049	A	G	22	GENIC	heterozygous	50044168
12	10344496	10344497	C	T	38	GENIC	heterozygous	51088297
12	10344577	10344578	A	G	27	GENIC	heterozygous	51088299
12	10344594	10344595	C	CT	26	GENIC	heterozygous	51088301
12	10344598	10344599	C	T	23	GENIC	heterozygous	51088303
12	10361735	10361736	T	G	22	GENIC	heterozygous	50044448
12	10364165	10364166	G	A	19	GENIC	heterozygous	50277212
12	10364166	10364167	A	C	19	GENIC	heterozygous	50277213
12	10364192	10364193	A	G	28	GENIC	heterozygous	50044466
12	10364220	10364221	G	A	25	GENIC	heterozygous	50044468
12	10364239	10364240	G	GA	28	GENIC	heterozygous	50044470
12	10364244	10364245	G	C	26	GENIC	heterozygous	50044472
12	10364247	10364248	T	C	26	GENIC	heterozygous	50044474
12	10364334	10364335	T	C	39	GENIC	heterozygous	50044476
12	10366149	10366150	G	A	32	GENIC	heterozygous	50044563
12	10372286	10372287	T	C	33	GENIC	heterozygous	50044903
12	10372289	10372290	C	T	32	GENIC	heterozygous	50044905
12	10372306	10372307	T	C	35	GENIC	heterozygous	50044907
12	10372378	10372379	C	T	25	GENIC	heterozygous	50044909
12	10385104	10385105	C	T	48	GENIC	heterozygous	50277242
12	10407619	10407620	C	T	29	GENIC	heterozygous	50277334
12	10408430	10408431	T	C	13	GENIC	heterozygous	50277340
12	10408448	10408449	T	C	18	GENIC	heterozygous	50277341
12	10408496	10408497	T	C	18	GENIC	heterozygous	50045305
12	10408512	10408513	T	G	18	GENIC	heterozygous	50277342
12	10408631	10408632	A	G	40	GENIC	heterozygous	50277343
12	10438846	10438847	C	T	9	GENIC	heterozygous	50277607
12	10438887	10438888	A	T	14	GENIC	heterozygous	50277608