chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	74241179	74241180	C	T	11	GENIC	heterozygous	116636663
10	74241318	74241319	G	T	11	GENIC	heterozygous	116636667
10	74241730	74241731	A	G	11	GENIC	heterozygous	116636671
10	74241871	74241872	C	G	22	GENIC	heterozygous	116636675
10	74241996	74241997	A	T	24	GENIC	homozygous	118001365
10	74242538	74242539	G	T	13	GENIC	heterozygous	116636677
10	74242656	74242657	G	C	6	GENIC	heterozygous	116636679
10	74243055	74243056	G	T	11	GENIC	heterozygous	116636683
10	74243732	74243733	C	T	11	GENIC	heterozygous	116636695
10	74243733	74243734	G	C	12	GENIC	heterozygous	116636697
10	74243963	74243964	A	G	17	GENIC	heterozygous	116636699
10	74244086	74244087	T	C	14	GENIC	heterozygous	116636703
10	74244107	74244108	C	G	15	GENIC	heterozygous	116636705
10	74244201	74244202	G	A	14	GENIC	heterozygous	116636711
10	74244297	74244298	G	T	17	GENIC	heterozygous	116636713
10	74244441	74244442	G	T	13	GENIC	heterozygous	116636715
10	74244498	74244499	G	C	23	GENIC	heterozygous	116636717
10	74244562	74244563	G	T	12	GENIC	heterozygous	116636719
10	74244867	74244868	C	T	13	GENIC	heterozygous	116636721
10	74245078	74245079	A	G	15	GENIC	heterozygous	116800146
10	74244439	74244440	C	A	13	GENIC	heterozygous	116800144
10	74245183	74245184	T	C	12	GENIC	heterozygous	116636727
10	74245914	74245915	T	C	15	GENIC	homozygous	117257089
10	74246862	74246863	G	T	13	GENIC	homozygous	117278393
10	74246914	74246915	C	T	14	GENIC	homozygous	117064320
10	74247473	74247474	T	C	13	GENIC	homozygous	116636731
10	74247517	74247518	C	G	16	GENIC	homozygous	116636733
10	74247938	74247939	C	T	7	GENIC	homozygous	116636739
10	74248011	74248012	A	G	8	GENIC	homozygous	116636741
10	74298518	74298519	G	A	3	GENIC	heterozygous	116636896