chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	51435359	51435360	C	G	34	GENIC	homozygous	112507241
15	51436476	51436477	C	T	43	GENIC	homozygous	112507243
15	51437259	51437259		TATC	22	GENIC	homozygous	129255671
15	51438610	51438611	A	G	31	GENIC	homozygous	112507245
15	51438635	51438636	A		34	GENIC	homozygous	129255672
15	51439318	51439318		AAAC	29	GENIC	homozygous	129255673
15	51439930	51439931	C	A	10	GENIC	homozygous	118918613
15	51440537	51440538	C	T	37	GENIC	homozygous	112507247
15	51440864	51440865	A	G	15	GENIC	homozygous	118918614
15	51441173	51441174	C		5	GENIC	homozygous	129255674
15	51457159	51457160	T		38	GENIC	homozygous	129255675
15	51459053	51459053		A	37	GENIC	possibly homozygous	129255676
15	51461080	51461081	A	G	52	GENIC	homozygous	112507259
15	51456014	51456015	C	A	36	GENIC	homozygous	112507249
15	51456070	51456071	G	A	33	GENIC	homozygous	112507251
15	51456844	51456845	G	T	28	GENIC	homozygous	118918616
15	51457249	51457250	C	T	35	GENIC	homozygous	112507253
15	51459576	51459577	T	G	37	GENIC	homozygous	112507255
15	51460342	51460343	G	T	43	GENIC	homozygous	112507257
15	51441171	51441172	A	C	5	GENIC	homozygous	129316746
15	51456856	51456857	T	G	20	GENIC	heterozygous	129316747
15	51453746	51453747	G	A	15	GENIC	possibly homozygous	113054309
15	51456855	51456856	T	G	20	GENIC	heterozygous	131939890
15	51461224	51461225	G	A	48	GENIC	homozygous	112507261
15	51461259	51461260	A	G	51	GENIC	homozygous	112507263
15	51461962	51461963	C	T	44	GENIC	homozygous	112507265
15	51462003	51462025	TCAGGATGGAGGGTGACACACT		34	GENIC	homozygous	129255677
15	51462532	51462533	C	G	50	GENIC	homozygous	112507267
15	51463287	51463288	G	A	49	GENIC	homozygous	112507269
15	51463693	51463693		CCT	46	GENIC	homozygous	129255678
15	51463737	51463738	A	G	45	GENIC	homozygous	113070660