chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	237136313	237136314	C	T	28	GENIC	homozygous	59946237
2	237136597	237136598	G	A	30	GENIC	homozygous	59946238
2	237136646	237136647	G	T	20	GENIC	homozygous	59454900
2	237136974	237136975	T	TTCTGTGTGTGTGTGTG	4	GENIC	homozygous	61940694
2	237137488	237137489	A	G	13	GENIC	homozygous	59946240
2	237137508	237137509	T	TTGGTTC	9	GENIC	homozygous	60595768
2	237137510	237137511	A	ACT	8	GENIC	possibly homozygous	60595770
2	237137511	237137512	G	GGAGGGCAACATGTAGAGGAATGC	8	GENIC	possibly homozygous	60595772
2	237137602	237137603	G	A	12	GENIC	homozygous	59946242
2	237137653	237137654	G	A	12	GENIC	homozygous	59946243
2	237137826	237137827	A	G	25	GENIC	homozygous	59946244
2	237137909	237137919	TTTCCTAAGA	----------	36	GENIC	homozygous	59946245
2	237138042	237138043	G	T	29	GENIC	homozygous	59946246
2	237138080	237138081	G	GT	12	GENIC	heterozygous	59776830
2	237138080	237138081	G	GTTTT	12	GENIC	heterozygous	60522107
2	237138101	237138102	C	G	23	GENIC	homozygous	59946247
2	237138175	237138176	C	T	21	GENIC	homozygous	59946248
2	237138400	237138401	C	A	21	GENIC	homozygous	59946249
2	237138489	237138490	T	C	27	GENIC	homozygous	59946250
2	237138718	237138719	C	T	21	GENIC	homozygous	59946251
2	237139012	237139013	T	C	24	GENIC	homozygous	59946252
2	237139239	237139240	A	G	20	GENIC	homozygous	59946253
2	237139830	237139831	A	G	43	GENIC	homozygous	59454906
2	237139927	237139928	G	A	35	GENIC	homozygous	59454907
2	237140757	237140759	CA	--	14	GENIC	homozygous	59454910