chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	25039966	25039967	T	A	31	GENIC	homozygous	110309751
18	25041247	25041248	A	G	13	GENIC	homozygous	110309753
18	25041447	25041448	G	A	16	GENIC	homozygous	110309755
18	25042443	25042444	C	T	38	GENIC	homozygous	110309757
18	25043238	25043239	T	C	28	GENIC	homozygous	110309759
18	25044806	25044807	T	G	24	GENIC	homozygous	110309761
18	25046211	25046212	G	A	42	GENIC	homozygous	110309763
18	25046231	25046232	C	T	41	GENIC	homozygous	110309765
18	25047729	25047730	A	G	25	GENIC	homozygous	110309767
18	25048165	25048166	C	G	39	GENIC	homozygous	119485436
18	25048779	25048780	C	T	17	GENIC	homozygous	110309769
18	25049039	25049040	A	G	23	GENIC	homozygous	110309773
18	25050774	25050775	T	C	23	GENIC	homozygous	110309775
18	25052796	25052797	C	T	35	GENIC	homozygous	110309777
18	25052852	25052853	G	A	33	GENIC	homozygous	110309778
18	25052981	25052982	G	A	41	GENIC	possibly homozygous	110832264
18	25053064	25053065	A	G	51	GENIC	heterozygous	119485438
18	25053073	25053074	G	A	50	GENIC	heterozygous	119485439
18	25053110	25053111	G	A	27	GENIC	possibly homozygous	119485440
18	25053279	25053280	T	G	37	GENIC	homozygous	119485444
18	25053553	25053554	T	A	17	GENIC	homozygous	110309779
18	25057309	25057310	G	A	34	GENIC	homozygous	110309780
18	25057746	25057747	G	A	28	GENIC	homozygous	110647645
18	25057937	25057938	C	T	31	GENIC	homozygous	110309781
18	25060898	25060899	T	C	34	GENIC	homozygous	110309782
18	25063727	25063728	C	T	30	GENIC	homozygous	110309783
18	25063890	25063891	G	A	32	GENIC	homozygous	110309784
18	25064071	25064072	G	T	19	GENIC	homozygous	110309785
18	25064281	25064282	C	A	23	GENIC	homozygous	110309786