chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	10843245	10843247	CC	--	1	GENIC	homozygous	50047318
12	10845322	10845323	C	G	13	GENIC	heterozygous	50047326
12	10846697	10846701	TGTG	----	6	GENIC	heterozygous	50047363
12	10847299	10847300	C	T	14	GENIC	homozygous	50047367
12	10847436	10847437	C	T	4	GENIC	homozygous	50047369
12	10848739	10848741	GT	--	2	GENIC	homozygous	50047381
12	10849585	10849589	ACAT	----	12	GENIC	homozygous	50047385
12	10849746	10849747	A	G	26	GENIC	possibly homozygous	50047387
12	10850340	10850341	C	G	11	GENIC	possibly homozygous	50047389
12	10851086	10851087	T	TC	20	GENIC	possibly homozygous	50047391
12	10851334	10851335	G	GA	2	GENIC	homozygous	50047393
12	10851351	10851352	T	A	2	GENIC	homozygous	50047395
12	10851363	10851364	A	C	4	GENIC	heterozygous	50047397
12	10852168	10852240	GGGCGAGCATCCGACTCAGCCTGGTTTGCTCTGTGCGGGCGAGCATCCGACTCAGCCTGGTTTGCTCTGTGC	------------------------------------------------------------------------	17	GENIC	homozygous	50503697
12	10852495	10852496	C	T	1	GENIC	homozygous	50503698
12	10852043	10852044	A	C	15	GENIC	possibly homozygous	50047405
12	10852456	10852457	T	C	15	GENIC	homozygous	50047407
12	10853558	10853559	A	G	21	GENIC	possibly homozygous	50047421
12	10854391	10854392	G	A	12	GENIC	homozygous	50047423
12	10855957	10855958	G	C	12	GENIC	possibly homozygous	50047435
12	10856148	10856149	C	T	24	GENIC	homozygous	50047437
12	10856801	10856802	A	ACAGGCTCT	4	GENIC	heterozygous	50047443
12	10857007	10857008	T	C	7	GENIC	possibly homozygous	50047445
12	10857217	10857218	C	CT	8	GENIC	homozygous	50047447
12	10857314	10857315	G	A	14	GENIC	possibly homozygous	50047449
12	10857874	10857875	G	A	9	GENIC	homozygous	50047451