chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	124070722	124070723	T	C	23	GENIC	homozygous	112393828
3	124075101	124075102	A	T	31	GENIC	homozygous	112393829
3	124078637	124078638	G	A	15	GENIC	homozygous	112393831
3	124085213	124085214	A	C	13	GENIC	homozygous	111693419
3	124086782	124086783	G	C	24	GENIC	homozygous	111693424
3	124094023	124094024	G	A	43	GENIC	homozygous	112393832
3	124094588	124094589	C	T	33	GENIC	homozygous	119739844
3	124094611	124094612	A	G	32	GENIC	homozygous	112393833
3	124094739	124094740	A	G	32	GENIC	homozygous	111693436
3	124095077	124095078	G	C	30	GENIC	homozygous	112393834
3	124095719	124095720	G	A	39	GENIC	homozygous	111693437
3	124095868	124095869	A	C	10	GENIC	homozygous	111693438
3	124096324	124096325	A	T	46	GENIC	homozygous	111693441
3	124096420	124096421	C	T	33	GENIC	homozygous	119685347
3	124096679	124096680	T	C	31	GENIC	homozygous	111693442
3	124096691	124096692	C	T	26	GENIC	homozygous	111693443
3	124096821	124096822	T	C	12	GENIC	homozygous	111693444
3	124097026	124097027	C	T	23	GENIC	homozygous	111693445
3	124099749	124099750	C	T	30	GENIC	homozygous	111693448
3	124099803	124099804	T	C	23	GENIC	homozygous	111693449
3	124100384	124100385	A	G	42	GENIC	homozygous	111693452
3	124100847	124100848	C	T	26	GENIC	homozygous	112393835
3	124101035	124101036	A	T	27	GENIC	homozygous	112027535
3	124101036	124101037	T	C	28	GENIC	homozygous	112027537
3	124102742	124102743	C	T	32	GENIC	homozygous	112393836
3	124102746	124102747	C	T	32	GENIC	homozygous	111693456
3	124102867	124102868	C	T	36	GENIC	homozygous	111693457
3	124103139	124103140	A	G	32	GENIC	homozygous	111693460
3	124103450	124103451	T	A	18	GENIC	homozygous	111693463
3	124103451	124103452	T	C	18	GENIC	homozygous	111693464
3	124103672	124103673	C	T	32	GENIC	homozygous	111693467