chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12259316	12259317	T	C	42	GENIC	homozygous	118404797
7	12260510	12260511	G	T	22	GENIC	possibly homozygous	116274516
7	12261426	12261427	A	G	38	GENIC	homozygous	115569720
7	12262104	12262105	A	G	30	GENIC	homozygous	116316535
7	12262958	12262959	G	A	26	GENIC	homozygous	116274520
7	12263312	12263313	A	G	40	GENIC	homozygous	116274522
7	12263975	12263976	G	A	40	GENIC	homozygous	116316537
7	12264861	12264862	A	G	30	GENIC	homozygous	116274524
7	12265001	12265002	T	C	21	GENIC	homozygous	116274526
7	12265018	12265019	A	G	24	GENIC	homozygous	115569725
7	12267080	12267081	A	G	33	GENIC	homozygous	116274530
7	12267566	12267567	G	T	39	GENIC	homozygous	115569726
7	12268263	12268264	G	A	23	GENIC	homozygous	116316539
7	12268849	12268850	C	T	24	GENIC	possibly homozygous	116316541
7	12268959	12268960	C	T	26	GENIC	homozygous	116316543
7	12271275	12271276	T	C	21	GENIC	homozygous	115569728
7	12272465	12272466	C	T	19	GENIC	homozygous	116316545
7	12272933	12272934	A	T	12	GENIC	homozygous	116316547
7	12273229	12273230	T	C	25	GENIC	homozygous	115569729
7	12273715	12273716	G	A	22	GENIC	homozygous	116316551
7	12273810	12273811	C	G	23	GENIC	homozygous	115569730
7	12273936	12273937	G	A	24	GENIC	homozygous	116316553
7	12274551	12274552	T	G	38	GENIC	homozygous	115569731
7	12274599	12274600	C	T	43	GENIC	homozygous	116316555
7	12275432	12275433	T	C	21	GENIC	homozygous	115569734
7	12275611	12275612	T	C	33	GENIC	homozygous	115569735
7	12275697	12275698	T	C	26	GENIC	homozygous	115569736
7	12275700	12275701	T	G	25	GENIC	homozygous	115569737
7	12276334	12276335	T	C	28	GENIC	homozygous	115569739
7	12276942	12276943	C	T	36	GENIC	homozygous	116316557
7	12278780	12278781	T	C	23	GENIC	homozygous	115569742
7	12278988	12278989	C	T	20	GENIC	homozygous	116316561
7	12279252	12279253	A	G	20	GENIC	homozygous	115569744
7	12279656	12279657	G	A	31	GENIC	homozygous	116316563
7	12279786	12279787	G	T	28	GENIC	homozygous	116316565