chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	43670599	43670600	A	-	38	GENIC	homozygous	48688204
14	43671925	43671926	A	G	52	GENIC	homozygous	48688205
14	43672183	43672184	T	TATAAA	29	GENIC	homozygous	48688206
14	43672337	43672338	T	C	38	GENIC	homozygous	48688207
14	43672771	43672772	G	A	51	GENIC	homozygous	48688208
14	43672956	43672957	A	G	44	GENIC	homozygous	48688209
14	43673437	43673438	A	T	53	GENIC	homozygous	48688210
14	43673816	43673817	C	T	52	GENIC	homozygous	48688211
14	43673943	43673945	TT	--	2	GENIC	homozygous	48688212
14	43673989	43673990	C	CCTTG	17	GENIC	possibly homozygous	48688213
14	43674362	43674363	G	A	51	GENIC	homozygous	48688214
14	43674375	43674376	T	C	46	GENIC	homozygous	48688215
14	43674549	43674550	C	G	38	GENIC	homozygous	48688216
14	43674950	43674951	G	T	42	GENIC	homozygous	48688217
14	43675062	43675063	A	ACCC	3	GENIC	homozygous	48688219
14	43675070	43675071	C	CCCCG	17	GENIC	heterozygous	48688220
14	43675113	43675116	AAA	---	21	GENIC	homozygous	48688221
14	43675119	43675120	A	G	25	GENIC	homozygous	48688222
14	43675253	43675254	C	T	49	GENIC	homozygous	48688223
14	43675662	43675663	A	G	38	GENIC	homozygous	48688224
14	43676623	43676624	A	G	38	GENIC	homozygous	48688225
14	43673451	43673452	T	G	49	GENIC	heterozygous	49251504