chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51008871	51008872	A	G	22	GENIC	homozygous	114342307
13	51008938	51008939	C	T	11	GENIC	homozygous	114342309
13	51009002	51009003	C	A	24	GENIC	homozygous	114342311
13	51009057	51009058	G	A	26	GENIC	homozygous	114342313
13	51009089	51009090	G	T	17	GENIC	homozygous	114342315
13	51009374	51009375	C	G	29	GENIC	homozygous	114342317
13	51009466	51009467	C	T	27	GENIC	homozygous	114342319
13	51009813	51009814	C	T	26	GENIC	homozygous	114342321
13	51009836	51009837	T	A	27	GENIC	homozygous	114342323
13	51009924	51009925	A	G	29	GENIC	homozygous	114342325
13	51010094	51010095	G	A	7	GENIC	heterozygous	126066682
13	51010095	51010096	T	C	7	GENIC	heterozygous	126066683
13	51010247	51010248	G	A	12	GENIC	heterozygous	118450728
13	51010360	51010361	C	T	14	GENIC	heterozygous	118450729
13	51010697	51010698	T	C	23	GENIC	homozygous	114342327
13	51010981	51010982	C	T	26	GENIC	possibly homozygous	114857610
13	51011588	51011589	C	T	16	GENIC	homozygous	114342329
13	51014436	51014437	T	C	11	GENIC	homozygous	114342331
13	51014486	51014487	A	T	4	GENIC	homozygous	114342333
13	51014706	51014707	A	G	21	GENIC	homozygous	114342337
13	51014749	51014750	G	A	9	GENIC	homozygous	114342339
13	51014954	51014955	T	A	10	GENIC	homozygous	114342341
13	51015007	51015008	G	A	22	GENIC	homozygous	114857612
13	51016418	51016419	G	A	8	GENIC	homozygous	114342343
13	51016710	51016711	C	T	22	GENIC	homozygous	114342345
13	51017051	51017052	A	G	17	GENIC	homozygous	114342347
13	51017452	51017453	T	G	28	GENIC	homozygous	114342349
13	51017951	51017952	A	G	12	GENIC	homozygous	114342351
13	51018047	51018048	A	C	7	GENIC	homozygous	114342353