chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10211169	10211170	T	C	14	GENIC	homozygous	155133439
20	10211169	10211170	T	G	14	GENIC	heterozygous	403464000
20	10211190	10211191	G	A	14	GENIC	homozygous	140515020
20	10211356	10211357	G	T	20	GENIC	homozygous	130051562
20	10214800	10214801	C	G	18	GENIC	homozygous	130051569
20	10216305	10216306	A	G	24	GENIC	homozygous	130051578
20	10217657	10217658	A	G	11	GENIC	homozygous	140515021
20	10219992	10219993	T	G	19	GENIC	homozygous	130051595
20	10222811	10222812	A	G	16	GENIC	homozygous	140515022
20	10222825	10222826	A	G	18	GENIC	homozygous	130051602
20	10223135	10223136	C	T	22	GENIC	homozygous	140515023
20	10223376	10223377	G	A	22	GENIC	homozygous	140515024
20	10224077	10224078	T	C	27	GENIC	homozygous	130051611
20	10224710	10224711	C	T	19	GENIC	homozygous	140515025
20	10218631	10218631		CTCT	14	GENIC	homozygous	140484755
20	10212062	10212062		A	12	GENIC	homozygous	140484753
20	10216371	10216371		G	27	GENIC	homozygous	140484754
20	10225487	10225488	C	T	12	GENIC	homozygous	140515026
20	10225893	10225894	A	G	23	GENIC	homozygous	130051613
20	10226570	10226571	C	T	25	GENIC	homozygous	140515027
20	10227407	10227408	C	T	24	GENIC	homozygous	140515028
20	10228253	10228254	T	C	18	GENIC	homozygous	130051615
20	10228354	10228355	A	G	24	GENIC	homozygous	130051616
20	10228362	10228363	C	T	24	GENIC	homozygous	130051617
20	10228382	10228383	G	A	28	GENIC	homozygous	130051618
20	10228475	10228476	G		11	GENIC	homozygous	129982678
20	10228504	10228505	C	T	11	GENIC	homozygous	130051620
20	10228518	10228519	C	T	12	GENIC	homozygous	130051621
20	10228533	10228534	G	T	7	GENIC	homozygous	130051622
20	10229619	10229620	C	G	21	GENIC	homozygous	130051625
20	10229625	10229626	T	C	20	GENIC	homozygous	140515029
20	10229628	10229628		TCCCGGTC	21	GENIC	homozygous	140484756
20	10229630	10229630		GCTGTCAATG	21	GENIC	homozygous	140484757
20	10230359	10230360	G	A	27	GENIC	homozygous	130051626