chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	44535080	44535081	G		22	GENIC	homozygous	129048675
13	44535083	44535086	GAG		23	GENIC	homozygous	129048676
13	44535098	44535099	C		18	GENIC	homozygous	129048677
13	44535121	44535122	T		13	GENIC	homozygous	129048678
13	44535125	44535127	CA		13	GENIC	homozygous	129048679
13	44535139	44535141	CA		12	GENIC	homozygous	129048680
13	44535146	44535147	G		12	GENIC	homozygous	129048681
13	44535159	44535160	T		9	GENIC	homozygous	129048682
13	44535493	44535494	A		9	GENIC	homozygous	129048684
13	44535505	44535508	TTT		11	GENIC	homozygous	129048685
13	44535517	44535517		A	11	GENIC	homozygous	129048686
13	44535520	44535520		A	11	GENIC	homozygous	129048687
13	44535527	44535528	A		11	GENIC	homozygous	129048688
13	44535549	44535550	C		15	GENIC	homozygous	129048689
13	44535557	44535558	G		17	GENIC	homozygous	129048690
13	44535575	44535576	T	A	18	GENIC	homozygous	118449756
13	44535592	44535592		C	18	GENIC	homozygous	129048691
13	44535599	44535600	C		16	GENIC	homozygous	129048692
13	44535618	44535619	T		17	GENIC	homozygous	129048693
13	44535646	44535647	C		15	GENIC	homozygous	129048694
13	44535653	44535657	AAGA		15	GENIC	homozygous	129048695
13	44535668	44535669	G		16	GENIC	homozygous	129048696
13	44535671	44535671		C	16	GENIC	homozygous	129048697
13	44550615	44550616	C	G	28	GENIC	homozygous	114334691
13	44535675	44535677	AC		16	GENIC	heterozygous	130690403
13	44550483	44550484	C	A	12	GENIC	possibly homozygous	114967687