chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39256517	39256518	T	C	9	GENIC	homozygous	116799878
8	39256560	39256561	T	C	16	GENIC	homozygous	116462783
8	39257415	39257416	T	A	14	GENIC	homozygous	116462788
8	39257436	39257437	C	T	12	GENIC	homozygous	116799880
8	39258192	39258193	C	G	13	GENIC	homozygous	116799882
8	39258539	39258540	T	C	11	GENIC	homozygous	116462798
8	39259531	39259532	T	A	23	GENIC	homozygous	116799884
8	39260318	39260319	T	C	11	GENIC	heterozygous	116941746
8	39260638	39260639	A	G	16	GENIC	homozygous	116462815
8	39261416	39261417	G	A	13	GENIC	homozygous	116799886
8	39261753	39261754	T	C	25	GENIC	homozygous	116462836
8	39261813	39261814	A	C	17	GENIC	homozygous	116462838
8	39262676	39262677	A	G	20	GENIC	homozygous	116462847
8	39262772	39262773	G	T	11	GENIC	heterozygous	116799888
8	39264033	39264034	A	G	18	GENIC	homozygous	116462859
8	39264107	39264108	C	T	7	GENIC	homozygous	116799890
8	39265392	39265393	T	C	15	GENIC	homozygous	116799896
8	39267472	39267473	T	A	25	GENIC	homozygous	116799898
8	39267510	39267511	C	G	9	GENIC	heterozygous	116799900
8	39267514	39267515	C	G	10	GENIC	heterozygous	116462892
8	39267884	39267885	G	T	20	GENIC	homozygous	116462904
8	39268072	39268073	A	G	31	GENIC	homozygous	116462906
8	39268492	39268493	T	C	15	GENIC	homozygous	116799902
8	39268503	39268504	T	C	12	GENIC	homozygous	116462912
8	39270222	39270223	A	G	27	GENIC	homozygous	116462927
8	39270259	39270260	C	A	17	GENIC	homozygous	116799904
8	39270473	39270474	A	G	18	GENIC	homozygous	116799906
8	39270657	39270658	A	G	21	GENIC	homozygous	116462928