chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40467431	40467432	C	T	10	GENIC	homozygous	115328180
12	40468040	40468041	T	A	21	GENIC	homozygous	115383811
12	40468275	40468276	A	G	28	GENIC	homozygous	115328182
12	40468623	40468624	C	T	13	GENIC	homozygous	115328184
12	40468982	40468983	C	T	21	GENIC	homozygous	115328186
12	40471718	40471719	A	C	9	GENIC	homozygous	115328188
12	40471835	40471836	A	T	24	GENIC	homozygous	115328190
12	40471968	40471969	T	A	4	GENIC	homozygous	115633283
12	40473723	40473724	A	G	14	GENIC	homozygous	115328193
12	40477088	40477089	T	C	24	GENIC	homozygous	115328201
12	40480636	40480637	C	T	4	GENIC	homozygous	118326988
12	40483212	40483213	C	A	11	GENIC	homozygous	115383825
12	40483217	40483218	G	A	8	GENIC	homozygous	115426776
12	40483422	40483423	G	T	24	GENIC	homozygous	115328205
12	40484593	40484594	T	C	9	GENIC	homozygous	118270545
12	40487376	40487377	C	T	19	GENIC	homozygous	115328209
12	40487460	40487461	T	C	11	GENIC	homozygous	115328211
12	40487519	40487520	C	T	17	GENIC	homozygous	115328213
12	40487596	40487597	T	C	8	GENIC	homozygous	115328215
12	40487606	40487607	C	T	12	GENIC	homozygous	115328217
12	40487658	40487659	G	A	5	GENIC	homozygous	115328219
12	40488148	40488149	A	C	7	GENIC	homozygous	115328225
12	40488759	40488760	G	A	16	GENIC	homozygous	115643746
12	40489937	40489938	G	T	9	GENIC	homozygous	115328227
12	40495881	40495882	G	A	13	GENIC	homozygous	115328233
12	40497113	40497114	T	C	9	GENIC	homozygous	115328235
12	40497657	40497658	C	T	5	GENIC	homozygous	115383845
12	40497811	40497812	C	T	4	GENIC	homozygous	115486352
12	40497816	40497817	G	A	6	GENIC	homozygous	115477539
12	40498039	40498040	C	T	14	GENIC	homozygous	115383847
12	40498317	40498318	A	T	14	GENIC	homozygous	115328237
12	40498437	40498438	T	C	8	GENIC	homozygous	115328239
12	40498449	40498450	T	C	5	GENIC	homozygous	115328241
12	40498463	40498464	G	A	8	GENIC	homozygous	115328243
12	40498778	40498779	A	G	12	GENIC	homozygous	115328247