chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	104338962	104338963	A		20	GENIC	homozygous	129190535
14	104338964	104338965	A	C	20	GENIC	homozygous	114093210
14	104350691	104350691		T	26	GENIC	homozygous	129190543
14	104356915	104356965	TGGATGGATGGGGGATGGATAGATGGATGGGTGATGGATGGATAGCTGGG		9	GENIC	homozygous	129190547
14	104370913	104370913		A	16	GENIC	homozygous	129190549
14	104370916	104370916		GGTA	16	GENIC	homozygous	129190550
14	104370918	104370918		AGGTACA	18	GENIC	homozygous	129190551
14	104370922	104370922		TCCTTAAGA	17	GENIC	homozygous	129190552
14	104370924	104370924		AAAAAAAAGGAACAAAAG	17	GENIC	homozygous	129190553
14	104370927	104370927		TGTCTATATTCAATATCACAGAAA	19	GENIC	homozygous	129190554
14	104370931	104370931		TTCCTTAAATAGG	20	GENIC	homozygous	129190555
14	104370933	104370934	A		18	GENIC	homozygous	129190556
14	104370936	104370936		A	18	GENIC	homozygous	129190557
14	104370940	104370940		TTT	18	GENIC	homozygous	129190558
14	104370942	104370942		TTTTATTT	18	GENIC	homozygous	129190559
14	104370943	104370944	G	T	20	GENIC	homozygous	123968508
14	104370949	104370949		TTT	21	GENIC	homozygous	129190560
14	104370951	104370952	G	T	19	GENIC	homozygous	123968510
14	104370956	104370960	TCCC		18	GENIC	homozygous	129190561
14	104370978	104370979	A		21	GENIC	homozygous	129190562
14	104370983	104370984	T	C	21	GENIC	homozygous	113529853
14	104370987	104370988	G	C	20	GENIC	homozygous	113529855
14	104370990	104370990		CCAA	19	GENIC	homozygous	129190563
14	104370994	104371003	AATTTAAAT		19	GENIC	homozygous	129190564
14	104371010	104371011	G	A	20	GENIC	homozygous	114093212
14	104371011	104371012	A	C	20	GENIC	homozygous	114093214
14	104371024	104371025	A	T	17	GENIC	homozygous	114124555
14	104371030	104371030		C	16	GENIC	homozygous	129190565
14	104371039	104371039		T	14	GENIC	homozygous	129190566
14	104374217	104374217		G	16	GENIC	homozygous	129190569