chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2644743	2644744	T	G	10	GENIC	homozygous	139064324
12	2644746	2644747	T	G	10	GENIC	homozygous	139064325
12	2644750	2644751	T	C	10	GENIC	homozygous	139064326
12	2663955	2663956	A	G	23	GENIC	homozygous	139064347
12	2664391	2664392	C	T	17	GENIC	homozygous	144915554
12	2667214	2667215	T	C	21	GENIC	homozygous	139064353
12	2667060	2667061	C	T	26	GENIC	homozygous	139064352
12	2668717	2668718	A	G	20	GENIC	homozygous	139064354
12	2668969	2668973	AGAC		13	GENIC	homozygous	139036225
12	2669407	2669408	A	C	17	GENIC	homozygous	144915555
12	2670025	2670026	C		14	GENIC	homozygous	139036226
12	2670154	2670155	G	A	14	GENIC	homozygous	144915556
12	2670192	2670197	AAAAC		14	GENIC	possibly homozygous	144912155
12	2670618	2670619	C	A	30	GENIC	homozygous	144915557
12	2672456	2672457	A	G	17	GENIC	homozygous	139064357
12	2672640	2672641	C	T	24	GENIC	homozygous	139064358
12	2672704	2672705	C	T	27	GENIC	homozygous	144915558
12	2672790	2672791	A	G	24	GENIC	homozygous	139064359
12	2675465	2675466	C	T	29	GENIC	homozygous	139064362
12	2677148	2677149	T	C	16	GENIC	homozygous	144915559
12	2677832	2677833	C	G	22	GENIC	homozygous	139064365
12	2679387	2679388	A	C	24	GENIC	homozygous	139064367
12	2670203	2670207	AAAC		16	GENIC	heterozygous	147800804
12	2672384	2672384		TTC	16	GENIC	heterozygous	144912156
12	2679710	2679710		CT	12	GENIC	possibly homozygous	144912157
12	2680702	2680702		A	24	GENIC	homozygous	144912158
12	2679348	2679349	C	T	24	GENIC	heterozygous	154753492
12	2680459	2680460	A	C	33	GENIC	homozygous	139064369
12	2681642	2681643	C	G	28	GENIC	homozygous	139064372
12	2682743	2682744	A	G	19	GENIC	homozygous	139064374
12	2683954	2683955	G	T	27	GENIC	homozygous	139064375
12	2684225	2684226	A	G	28	GENIC	homozygous	144915560
12	2679348	2679349	C		24	GENIC	homozygous	403313194