chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	127628056	127628057	A	G	23	GENIC	homozygous	110008751
2	127628245	127628246	T	G	16	GENIC	homozygous	110008752
2	127630254	127630255	T	C	15	GENIC	homozygous	110008753
2	127632664	127632665	G	T	16	GENIC	homozygous	110008754
2	127632740	127632741	A	G	21	GENIC	homozygous	110008755
2	127635216	127635217	T	C	20	GENIC	homozygous	110008756
2	127636322	127636323	A	G	18	GENIC	homozygous	110008759
2	127636447	127636448	C	T	17	GENIC	homozygous	110008760
2	127642081	127642082	C	T	20	GENIC	homozygous	110008770
2	127645184	127645185	A	G	16	GENIC	homozygous	110008771
2	127645728	127645729	T	C	31	GENIC	homozygous	110008772
2	127647328	127647329	C	T	22	GENIC	homozygous	110008773
2	127651756	127651757	C	A	14	GENIC	homozygous	110008776
2	127652304	127652305	G	T	24	GENIC	homozygous	110008777
2	127654318	127654319	C	T	20	GENIC	homozygous	110008778
2	127655866	127655867	A	G	21	GENIC	homozygous	110008779
2	127656126	127656127	C	T	31	GENIC	homozygous	110008780
2	127657300	127657301	T	A	9	GENIC	homozygous	110008781
2	127660484	127660485	C	T	13	GENIC	homozygous	110008783
2	127661229	127661230	T	C	24	GENIC	homozygous	110008784
2	127661425	127661426	T	C	28	GENIC	homozygous	110008785
2	127664583	127664584	A	G	23	GENIC	homozygous	110008786
2	127664768	127664769	A	G	22	GENIC	homozygous	110008787
2	127666753	127666754	A	C	21	GENIC	homozygous	110008788
2	127667391	127667392	T	C	11	GENIC	homozygous	110008789
2	127667510	127667511	G	T	10	GENIC	homozygous	110008790
2	127669849	127669850	A	G	20	GENIC	homozygous	110008791
2	127670955	127670956	A	G	17	GENIC	homozygous	110008792
2	127673491	127673492	G	T	19	GENIC	homozygous	110008794
2	127674167	127674168	T	C	20	GENIC	homozygous	110008795
2	127674168	127674169	A	G	21	GENIC	homozygous	110008796
2	127676881	127676882	T	C	28	GENIC	homozygous	110008797
2	127679155	127679156	A	T	21	GENIC	possibly homozygous	110008799
2	127680020	127680021	A	C	11	GENIC	homozygous	110008800