chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	108491086	108491087	T	C	25	GENIC	homozygous	113541344
14	108492575	108492576	T	C	37	GENIC	homozygous	113541346
14	108494917	108494918	A	C	7	GENIC	homozygous	118725429
14	108495283	108495284	G	C	13	GENIC	homozygous	118725430
14	108496413	108496414	G	A	6	GENIC	homozygous	114027029
14	108497000	108497001	C	G	6	GENIC	homozygous	118725431
14	108497006	108497007	A	G	6	GENIC	homozygous	118725432
14	108498973	108498974	T	C	28	GENIC	homozygous	113541348
14	108500231	108500232	G	A	23	GENIC	homozygous	113541350
14	108500328	108500329	G	C	30	GENIC	homozygous	113541352
14	108500632	108500633	A	G	40	GENIC	homozygous	113541354
14	108501160	108501161	G	T	33	GENIC	homozygous	113541356
14	108501545	108501546	C	A	15	GENIC	heterozygous	118850200
14	108505961	108505962	G	A	21	GENIC	homozygous	113541366
14	108502309	108502310	C	A	8	GENIC	homozygous	113541358
14	108502495	108502496	T	A	13	GENIC	homozygous	113541360
14	108502649	108502650	A	G	16	GENIC	homozygous	113541362
14	108505624	108505625	G	A	23	GENIC	homozygous	113541364
14	108504065	108504066	C	G	23	GENIC	homozygous	113789757
14	108505123	108505124	C	T	17	GENIC	homozygous	113695060
14	108507958	108507959	C	T	20	GENIC	homozygous	113541368
14	108509375	108509376	T	G	39	GENIC	homozygous	113541370
14	108510335	108510336	G	A	24	GENIC	homozygous	113541372
14	108511293	108511294	G	A	14	GENIC	homozygous	113541374
14	108511383	108511384	C	A	20	GENIC	possibly homozygous	113789759
14	108511532	108511533	A	G	13	GENIC	homozygous	113541376
14	108511866	108511867	G	A	16	GENIC	homozygous	113541378
14	108512264	108512265	C	T	13	GENIC	homozygous	113541380
14	108514018	108514019	A	G	37	GENIC	homozygous	113541382
14	108515726	108515727	G	A	14	GENIC	homozygous	113541384
14	108516013	108516014	T	C	24	GENIC	homozygous	113541386
14	108516799	108516800	T	C	34	GENIC	homozygous	113541388
14	108517480	108517481	G	T	23	GENIC	homozygous	113541390