chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	43883524	43883525	A		47	GENIC	homozygous	129152452
14	43885109	43885109		ATAAA	44	GENIC	homozygous	129152453
14	43886362	43886363	A	T	74	GENIC	possibly homozygous	113443756
14	43884850	43884851	A	G	45	GENIC	homozygous	113443748
14	43885262	43885263	T	C	49	GENIC	homozygous	113443750
14	43885696	43885697	G	A	56	GENIC	homozygous	113443752
14	43885881	43885882	A	G	52	GENIC	homozygous	113443754
14	43886741	43886742	C	T	55	GENIC	possibly homozygous	113443758
14	43886915	43886915		CTTG	39	GENIC	homozygous	129152454
14	43887287	43887288	G	A	43	GENIC	homozygous	113443760
14	43887300	43887301	T	C	43	GENIC	homozygous	113443762
14	43887474	43887475	C	G	58	GENIC	homozygous	113443764
14	43887875	43887876	G	T	41	GENIC	homozygous	113443766
14	43888038	43888041	AAA		26	GENIC	homozygous	129152455
14	43888044	43888045	A	G	26	GENIC	homozygous	113443768
14	43888178	43888179	C	T	46	GENIC	homozygous	113443770
14	43888587	43888588	A	G	52	GENIC	homozygous	113443772
14	43889548	43889549	A	G	63	GENIC	homozygous	113443774