chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51242772	51242773	A	G	12	GENIC	heterozygous	118598284
13	51243814	51243815	T	C	54	GENIC	heterozygous	118450767
13	51243822	51243823	C	T	54	GENIC	heterozygous	118591987
13	51244449	51244450	G	C	40	GENIC	homozygous	114342955
13	51245167	51245168	T	C	42	GENIC	homozygous	114857637
13	51246097	51246098	T	G	27	GENIC	possibly homozygous	118591988
13	51246287	51246288	G	A	37	GENIC	homozygous	114342971
13	51247718	51247719	T	A	22	GENIC	heterozygous	115087205
13	51252415	51252416	T	A	32	GENIC	homozygous	114343009
13	51252834	51252835	G	A	33	GENIC	homozygous	114343011
13	51254302	51254303	A	G	29	GENIC	homozygous	114343017
13	51257143	51257144	A	G	26	GENIC	homozygous	114890575
13	51243763	51243764	C	T	35	GENIC	homozygous	114890565
13	51246329	51246330	G	A	40	GENIC	homozygous	114890567
13	51250061	51250062	A	G	32	GENIC	homozygous	114890569
13	51256991	51256992	T	C	27	GENIC	homozygous	114890571
13	51257128	51257129	T	C	27	GENIC	homozygous	114890573
13	51251325	51251326	G	A	15	GENIC	homozygous	114672315
13	51257671	51257672	G	C	16	GENIC	homozygous	114890577
13	51258067	51258068	C	T	26	GENIC	homozygous	114890579
13	51258251	51258252	G	A	33	GENIC	homozygous	114890581
13	51258338	51258339	A	C	23	GENIC	homozygous	115010053
13	51258873	51258874	G	A	36	GENIC	homozygous	114890583
13	51258917	51258918	G	A	36	GENIC	homozygous	114890585
13	51258918	51258919	G	A	36	GENIC	homozygous	114890587
13	51259257	51259258	C	T	28	GENIC	possibly homozygous	114890589