chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40270951	40270952	G	T	49	GENIC	homozygous	115328003
12	40275731	40275732	G	A	39	GENIC	homozygous	115328005
12	40275735	40275736	G	A	38	GENIC	homozygous	115328007
12	40275744	40275745	T	G	40	GENIC	homozygous	115328009
12	40276358	40276359	T	C	45	GENIC	homozygous	115328011
12	40313861	40313862	C	G	32	GENIC	homozygous	115328013
12	40313871	40313872	C	A	33	GENIC	homozygous	115328015
12	40313887	40313888	C	A	33	GENIC	homozygous	115328017
12	40313893	40313894	C	A	33	GENIC	homozygous	115328019
12	40313908	40313909	G	A	34	GENIC	homozygous	115328021
12	40313912	40313913	C	A	33	GENIC	homozygous	115328023
12	40313920	40313921	C	A	35	GENIC	homozygous	115328025
12	40322611	40322612	G	A	55	GENIC	homozygous	115328027
12	40326937	40326938	C	T	45	GENIC	homozygous	115328029
12	40329811	40329812	A	G	28	GENIC	homozygous	115328031
12	40334432	40334433	G	A	42	GENIC	homozygous	115328033