chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	39391102	39391103	T	A	34	GENIC	homozygous	113266928
4	39391209	39391210	G	A	25	GENIC	homozygous	113266929
4	39391263	39391264	A	G	29	GENIC	homozygous	112596355
4	39391295	39391296	C	T	30	GENIC	homozygous	112596357
4	39391323	39391324	G	A	36	GENIC	homozygous	113266930
4	39391348	39391349	A	C	37	GENIC	homozygous	113266931
4	39391397	39391398	C	T	32	GENIC	homozygous	113266932
4	39391481	39391482	T	C	34	GENIC	homozygous	113266933
4	39391525	39391526	A	G	29	GENIC	homozygous	113266934
4	39391533	39391534	G	A	28	GENIC	homozygous	113266935
4	39391593	39391594	G	A	36	GENIC	homozygous	113266936
4	39391701	39391702	C	T	27	GENIC	homozygous	113266937
4	39391743	39391744	C	T	30	GENIC	possibly homozygous	113266938
4	39391745	39391746	T	C	31	GENIC	homozygous	113266939
4	39391858	39391859	G	A	28	GENIC	homozygous	113266940
4	39391861	39391862	G	T	29	GENIC	homozygous	113266941