chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	43670532	43670533	T	TA	11	GENIC	possibly homozygous	49540812
14	43670599	43670600	A	-	19	GENIC	homozygous	48688204
14	43671816	43671817	G	A	30	GENIC	homozygous	49587251
14	43671925	43671926	A	G	32	GENIC	homozygous	48688205
14	43672183	43672184	T	TATAAA	27	GENIC	homozygous	48688206
14	43672337	43672338	T	C	30	GENIC	homozygous	48688207
14	43672956	43672957	A	G	20	GENIC	homozygous	48688209
14	43672974	43672975	C	T	20	GENIC	possibly homozygous	49587252
14	43673437	43673438	A	T	27	GENIC	homozygous	48688210
14	43673802	43673803	G	A	34	GENIC	possibly homozygous	49587253
14	43673943	43673945	TT	--	18	GENIC	homozygous	48688212
14	43674375	43674376	T	C	23	GENIC	homozygous	48688215
14	43674426	43674427	G	A	19	GENIC	possibly homozygous	49587254
14	43674549	43674550	C	G	25	GENIC	homozygous	48688216
14	43674721	43674722	A	AG	24	GENIC	possibly homozygous	49587255
14	43675070	43675071	C	CCCCG	3	GENIC	homozygous	48688220
14	43675119	43675120	A	G	12	GENIC	homozygous	48688222
14	43675662	43675663	A	G	35	GENIC	homozygous	48688224
14	43676242	43676243	T	G	29	GENIC	homozygous	49587256
14	43676314	43676315	C	T	24	GENIC	homozygous	49587257
14	43676331	43676332	C	T	16	GENIC	homozygous	49587258
14	43676394	43676395	G	A	23	GENIC	homozygous	49587259
14	43676497	43676498	G	A	18	GENIC	homozygous	49587260
14	43676556	43676557	C	T	29	GENIC	homozygous	49587261
14	43676626	43676627	G	GC	25	GENIC	homozygous	49587262
14	43676633	43676634	C	T	27	GENIC	homozygous	49587263
14	43676737	43676738	C	T	27	GENIC	possibly homozygous	49587264
14	43676928	43676929	G	C	26	GENIC	possibly homozygous	49587265
14	43676335	43676336	T	TATGCAGTCAC	17	GENIC	homozygous	49589538
14	43674768	43674769	G	A	17	GENIC	possibly homozygous	49589536
14	43674773	43674774	G	A	17	GENIC	possibly homozygous	49589537