chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	31870660	31870661	T	C	75	GENIC	homozygous	50174560
12	31870699	31870700	A	G	69	GENIC	homozygous	50174561
12	31870739	31870740	C	T	61	GENIC	homozygous	50174562
12	31871182	31871190	CCATCCAT	--------	16	GENIC	homozygous	50734588
12	31872574	31872575	G	A	60	GENIC	homozygous	50931887
12	31874140	31874141	C	T	44	GENIC	homozygous	50931890
12	31874144	31874145	A	T	45	GENIC	homozygous	50931893
12	31874280	31874281	G	A	58	GENIC	homozygous	50174566
12	31875871	31875872	C	A	31	GENIC	homozygous	50931896
12	31876209	31876210	T	TTG	4	GENIC	homozygous	50541017
12	31876210	31876211	C	CATTTGAACAATAAAATACT	5	GENIC	heterozygous	50541018
12	31876212	31876213	G	GCAGCTGAAGC	5	GENIC	heterozygous	50541019
12	31876216	31876217	G	GGCAGAAGAACA	4	GENIC	heterozygous	50541020
12	31876231	31876232	A	-	8	GENIC	heterozygous	50562992
12	31876233	31876237	AGAA	----	9	GENIC	heterozygous	50562994
12	31876881	31876882	A	G	28	GENIC	homozygous	50174569
12	31876922	31876923	A	AC	10	GENIC	homozygous	50931899
12	31878777	31878779	TG	--	8	GENIC	heterozygous	50174572
12	31878778	31878782	GTTG	----	6	GENIC	heterozygous	50931902
12	31879440	31879441	G	A	51	GENIC	homozygous	50931905
12	31882171	31882172	A	AGGCAGGCG	57	GENIC	homozygous	50931908
12	31884692	31884693	T	C	29	GENIC	homozygous	50174579
12	31884910	31884911	T	TA	12	GENIC	homozygous	50174580
12	31885347	31885351	ACAC	----	2	GENIC	homozygous	50931914
12	31889730	31889731	A	C	30	GENIC	possibly homozygous	50174592
12	31889914	31889915	C	-	12	GENIC	homozygous	50931917
12	31893296	31893297	T	C	48	GENIC	homozygous	50931923
12	31893544	31893559	TAATAATATAGTGAT	---------------	1	GENIC	homozygous	50931926
12	31894098	31894099	A	T	31	GENIC	homozygous	50931929