chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40275731	40275732	G	A	21	GENIC	homozygous	115328005
12	40275735	40275736	G	A	20	GENIC	homozygous	115328007
12	40275743	40275743		A	20	GENIC	homozygous	128989139
12	40275744	40275745	T	G	20	GENIC	homozygous	115328009
12	40278185	40278185		CCCG	13	GENIC	homozygous	128989141
12	40278188	40278192	ATAG		14	GENIC	homozygous	128989142
12	40313861	40313862	C	G	13	GENIC	homozygous	115328013
12	40313871	40313872	C	A	10	GENIC	homozygous	115328015
12	40313887	40313888	C	A	12	GENIC	homozygous	115328017
12	40313893	40313894	C	A	11	GENIC	homozygous	115328019
12	40313908	40313909	G	A	10	GENIC	homozygous	115328021
12	40313912	40313913	C	A	10	GENIC	homozygous	115328023
12	40313920	40313921	C	A	9	GENIC	homozygous	115328025
12	40314365	40314365		TCTGTAATGGGATCTGATGCCTTCTTCTAGTGTGTCTGAAGACAGCTACAGTGTAC	9	GENIC	homozygous	128989146
12	40322048	40322048		C	10	GENIC	homozygous	128989147
12	40326937	40326938	C	T	18	GENIC	homozygous	115328029
12	40326939	40326941	CT		18	GENIC	homozygous	128989148
12	40326942	40326943	C		18	GENIC	homozygous	128989149
12	40326962	40326962		T	17	GENIC	homozygous	128989150