chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	113917163	113917164	A	C	30	GENIC	homozygous	111677955
3	113917179	113917180	G	T	35	GENIC	homozygous	111677956
3	113917184	113917185	G	T	38	GENIC	homozygous	111677957
3	113917203	113917204	G	T	34	GENIC	homozygous	111677958
3	113917205	113917206	G	T	35	GENIC	homozygous	111677959
3	113921616	113921617	C	A	25	GENIC	homozygous	111677978
3	113921630	113921631	G	T	25	GENIC	homozygous	111677979
3	113921656	113921657	A	T	24	GENIC	homozygous	111677980
3	113921665	113921666	G	T	24	GENIC	homozygous	111677981
3	113921670	113921671	G	T	23	GENIC	homozygous	111677982
3	113921675	113921676	G	T	23	GENIC	homozygous	111677983
3	113932052	113932053	T	C	17	GENIC	homozygous	111677997
3	113932062	113932063	G	A	13	GENIC	homozygous	111677998
3	113932065	113932066	C	A	13	GENIC	homozygous	111677999
3	113951981	113951982	C	A	38	GENIC	homozygous	111678017
3	113955889	113955890	G	T	28	GENIC	homozygous	119702419
3	113955891	113955892	C	G	28	GENIC	homozygous	119702420
3	113955894	113955895	C	A	28	GENIC	homozygous	119702421
3	113955905	113955906	G	A	24	GENIC	homozygous	111678024
3	113955933	113955934	G	C	23	GENIC	homozygous	111678025
3	113955943	113955944	C	A	25	GENIC	homozygous	119702422
3	113955944	113955945	A	G	24	GENIC	homozygous	119702423
3	113955948	113955949	A	G	23	GENIC	homozygous	111678026
3	113955950	113955951	C	A	22	GENIC	homozygous	111678027
3	113956487	113956488	G	C	23	GENIC	possibly homozygous	111678028