chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	49050514	49050515	T	TC	25	GENIC	possibly homozygous	50230908
12	49050515	49050516	T	TTTC	26	GENIC	possibly homozygous	50230910
12	49050523	49050524	A	C	35	GENIC	possibly homozygous	50230912
12	49050527	49050528	A	C	36	GENIC	possibly homozygous	50230914
12	49050531	49050532	A	C	34	GENIC	possibly homozygous	50230916
12	49050535	49050536	A	C	33	GENIC	homozygous	50230918
12	49050539	49050540	A	C	35	GENIC	homozygous	50230920
12	49050543	49050544	A	C	33	GENIC	homozygous	50230922
12	49050547	49050548	A	C	35	GENIC	heterozygous	50230924
12	49051394	49051395	C	A	46	GENIC	homozygous	50230926
12	49051755	49051756	G	-	38	GENIC	heterozygous	50230928
12	49052300	49052301	A	AGT	49	GENIC	homozygous	50230930
12	49052364	49052365	A	T	60	GENIC	possibly homozygous	50230932
12	49052768	49052769	T	C	53	GENIC	homozygous	50230934
12	49055395	49055396	A	C	68	GENIC	homozygous	50230936
12	49055667	49055668	G	GA	19	GENIC	heterozygous	50230938
12	49055716	49055717	T	TG	14	GENIC	heterozygous	50343654
12	49056077	49056078	C	CA	19	GENIC	homozygous	50230940
12	49056146	49056147	C	A	21	GENIC	homozygous	50230942