chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40270951	40270952	G	T	41	GENIC	homozygous	115328003
12	40275735	40275736	G	A	40	GENIC	homozygous	115328007
12	40275744	40275745	T	G	41	GENIC	homozygous	115328009
12	40277046	40277047	C	T	23	GENIC	homozygous	115494845
12	40292875	40292876	G	C	27	GENIC	homozygous	115383497
12	40293118	40293119	T	C	39	GENIC	homozygous	115383499
12	40294814	40294815	G	T	16	GENIC	homozygous	115494847
12	40294970	40294971	G	T	28	GENIC	homozygous	115494849
12	40295634	40295635	G	A	23	GENIC	homozygous	115494851
12	40309759	40309760	C	T	24	GENIC	homozygous	115383501
12	40313861	40313862	C	G	30	GENIC	homozygous	115328013
12	40313871	40313872	C	A	30	GENIC	homozygous	115328015
12	40313887	40313888	C	A	26	GENIC	homozygous	115328017
12	40313893	40313894	C	A	22	GENIC	homozygous	115328019
12	40313908	40313909	G	A	21	GENIC	homozygous	115328021
12	40313912	40313913	C	A	20	GENIC	homozygous	115328023
12	40313920	40313921	C	A	22	GENIC	homozygous	115328025
12	40319421	40319422	A	T	30	GENIC	homozygous	115383503
12	40325280	40325281	T	C	21	GENIC	homozygous	115383505
12	40326937	40326938	C	T	22	GENIC	homozygous	115328029
12	40329811	40329812	A	G	26	GENIC	homozygous	115328031
12	40334203	40334204	T	C	26	GENIC	homozygous	115383507
12	40334934	40334935	T	C	39	GENIC	homozygous	115383509