chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	107843900	107843901	G	A	10	GENIC	heterozygous	49188225
14	107843902	107843903	T	C	10	GENIC	possibly homozygous	48891656
14	107844771	107844772	A	G	11	GENIC	homozygous	49188227
14	107846656	107846657	C	A	6	GENIC	heterozygous	49455499
14	107846975	107846976	T	C	24	GENIC	possibly homozygous	49455500
14	107847797	107847798	T	-	10	GENIC	homozygous	49455501
14	107848164	107848165	C	T	18	GENIC	possibly homozygous	49455502
14	107849445	107849446	C	T	12	GENIC	homozygous	49188235
14	107849454	107849455	T	C	11	GENIC	homozygous	49188237
14	107849558	107849671	TAAAAAGTTTTATGTTGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGTAAGCACAAGGCCCTGGGTTATGTCCTCAGCTCCAAAAAAAAAGAAAGAAAGAAAGAAAAAG	-----------------------------------------------------------------------------------------------------------------	34	GENIC	heterozygous	49423042
14	107850436	107850437	T	C	14	GENIC	homozygous	49455503
14	107850731	107850732	T	A	14	GENIC	homozygous	49455504
14	107851366	107851367	A	C	25	GENIC	homozygous	49455505
14	107852146	107852147	C	CGCT	4	GENIC	homozygous	49485622
14	107852302	107852303	T	C	12	GENIC	possibly homozygous	49455506
14	107853586	107853587	G	T	12	GENIC	homozygous	49455507
14	107854130	107854131	G	A	13	GENIC	homozygous	49188245
14	107854144	107854145	G	A	5	GENIC	homozygous	49455508
14	107854320	107854321	G	GC	11	GENIC	homozygous	49455509
14	107854447	107854448	C	G	7	GENIC	homozygous	49455510