chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39614643	39614644	G	A	28	GENIC	homozygous	115326335
12	39615672	39615673	T	C	22	GENIC	homozygous	115326337
12	39615721	39615722	G	A	25	GENIC	homozygous	115326339
12	39615733	39615734	C	T	23	GENIC	homozygous	115326341
12	39616266	39616267	C	T	27	GENIC	homozygous	115326343
12	39616679	39616680	A	G	26	GENIC	homozygous	115326345
12	39617852	39617853	G	T	32	GENIC	homozygous	115326349
12	39619503	39619504	T	C	23	GENIC	homozygous	115326351
12	39619923	39619924	T	C	27	GENIC	homozygous	115326353
12	39620562	39620563	T	C	16	GENIC	homozygous	115326355
12	39620649	39620650	C	T	16	GENIC	homozygous	115326357
12	39622491	39622492	A	G	12	GENIC	homozygous	115326359
12	39623211	39623212	T	G	27	GENIC	homozygous	115326361
12	39625847	39625848	T	C	20	GENIC	homozygous	115326363
12	39627328	39627329	T	C	34	GENIC	homozygous	115326365
12	39633454	39633455	C	T	11	GENIC	homozygous	115326371
12	39633995	39633996	G	A	14	GENIC	homozygous	115326373
12	39636266	39636267	C	T	31	GENIC	homozygous	115326375
12	39636782	39636783	G	C	19	GENIC	homozygous	115326377
12	39638157	39638158	T	A	18	GENIC	homozygous	115326379
12	39638813	39638814	T	C	15	GENIC	homozygous	115326381
12	39639931	39639932	C	T	5	GENIC	homozygous	115383349
12	39640896	39640897	C	T	16	GENIC	homozygous	115326383