chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13284647	13284648	C	T	40	GENIC	homozygous	115260277
12	13284775	13284776	T	C	39	GENIC	homozygous	115260279
12	13284919	13284920	C	T	25	GENIC	homozygous	115260281
12	13284961	13284962	A	G	24	GENIC	homozygous	115260283
12	13285329	13285330	C	T	41	GENIC	homozygous	115260285
12	13286950	13286951	T	C	40	GENIC	homozygous	115260287
12	13287511	13287512	A	G	20	GENIC	homozygous	115260289
12	13288854	13288855	T	G	43	GENIC	homozygous	115260291
12	13289382	13289383	T	C	37	GENIC	homozygous	115260293
12	13290113	13290114	A	G	55	GENIC	homozygous	115260295
12	13291046	13291047	G	A	31	GENIC	homozygous	115260297
12	13291222	13291223	C	T	28	GENIC	homozygous	115260299
12	13291655	13291656	A	G	32	GENIC	homozygous	115260301
12	13291664	13291665	T	C	33	GENIC	homozygous	115260303
12	13291915	13291916	G	A	34	GENIC	homozygous	115260305
12	13293881	13293882	G	A	56	GENIC	heterozygous	118245343
12	13293474	13293475	G	T	68	GENIC	heterozygous	118245340
12	13293855	13293856	G	A	46	GENIC	heterozygous	118245341
12	13293859	13293860	G	A	50	GENIC	heterozygous	118245342
12	13293881	13293882	G	T	56	GENIC	heterozygous	118245344
12	13293884	13293885	G	A	58	GENIC	heterozygous	118245345
12	13293945	13293946	A	G	50	GENIC	heterozygous	118245346
12	13294128	13294129	C	T	10	GENIC	possibly homozygous	118245347
12	13294211	13294212	G	A	25	GENIC	heterozygous	118245351
12	13296348	13296349	T	C	30	GENIC	homozygous	115260307
12	13297641	13297642	C	T	45	GENIC	possibly homozygous	115260309