chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	124327470	124327471	C	T	12	GENIC	homozygous	54093270
7	124327666	124327669	TGG	---	3	GENIC	homozygous	54093272
7	124328069	124328070	A	AC	7	GENIC	homozygous	54093274
7	124328073	124328074	G	C	9	GENIC	homozygous	54093275
7	124328585	124328586	T	-	5	GENIC	homozygous	54093277
7	124328765	124328766	C	T	22	GENIC	possibly homozygous	54093279
7	124331461	124331462	C	T	16	GENIC	possibly homozygous	54093281
7	124331535	124331536	A	-	1	GENIC	homozygous	54093283
7	124332025	124332026	G	A	28	GENIC	homozygous	54093285
7	124332227	124332228	C	CTG	14	GENIC	possibly homozygous	54093287
7	124332305	124332306	C	T	8	GENIC	homozygous	54093289
7	124332308	124332309	T	G	7	GENIC	homozygous	54093290
7	124332351	124332352	C	T	15	GENIC	homozygous	54093292
7	124332432	124332433	T	C	22	GENIC	possibly homozygous	54093294
7	124333202	124333203	C	A	17	GENIC	homozygous	54093296
7	124333269	124333270	T	C	25	GENIC	possibly homozygous	54093298
7	124333423	124333424	G	A	22	GENIC	possibly homozygous	54093300
7	124333484	124333485	C	-	6	GENIC	homozygous	54093302
7	124334296	124334297	G	A	6	GENIC	homozygous	54093304
7	124334297	124334298	G	T	6	GENIC	homozygous	54093306
7	124334311	124334326	CTCACACCTGTCAAG	---------------	3	GENIC	heterozygous	54093308
7	124334728	124334729	A	AGT	3	GENIC	heterozygous	54093311
7	124334929	124334930	A	G	17	GENIC	homozygous	54093321
7	124335889	124335890	T	C	17	GENIC	possibly homozygous	54093323
7	124336368	124336369	C	T	15	GENIC	possibly homozygous	54093325
7	124337118	124337119	A	G	2	GENIC	homozygous	54093327
7	124338001	124338002	T	G	25	GENIC	homozygous	54093329
7	124340177	124340178	A	G	1	GENIC	homozygous	54093335
7	124340981	124340982	T	TCCCACGAGTCTGCAAGAGTGGCAAGC	1	GENIC	homozygous	54921567
7	124341649	124341650	A	-	21	GENIC	possibly homozygous	54093340
7	124342956	124342957	T	C	4	GENIC	homozygous	54093346
7	124343455	124343456	T	C	13	GENIC	homozygous	54093348
7	124344281	124344283	GA	--	7	GENIC	heterozygous	54093350
7	124344769	124344770	T	-	9	GENIC	homozygous	54093352
7	124345485	124345605	GCCAGATGACATTCTGTTTTTTTTTTTTTTTCTTTTCTTTTTTTTCGGAGCTGAGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCT	------------------------------------------------------------------------------------------------------------------------	15	GENIC	possibly homozygous	54921569
7	124346174	124346175	C	T	15	GENIC	possibly homozygous	54093354
7	124346502	124346503	C	T	22	GENIC	possibly homozygous	54093356
7	124346789	124346790	C	T	11	GENIC	homozygous	54093358
7	124347109	124347110	C	T	26	GENIC	heterozygous	54093360
7	124348554	124348555	C	T	15	GENIC	heterozygous	54093362
7	124349393	124349394	G	A	17	GENIC	possibly homozygous	54093372
7	124350131	124350132	A	AAC	6	GENIC	heterozygous	54093376
7	124351550	124351551	C	T	18	GENIC	homozygous	54093378
7	124351759	124351760	T	-	1	GENIC	homozygous	54238079
7	124352258	124352259	G	T	24	GENIC	possibly homozygous	54093382
7	124353400	124353401	G	A	8	GENIC	homozygous	54093384
7	124354886	124354887	T	TAAC	12	GENIC	homozygous	54093386
7	124355060	124355061	T	C	27	GENIC	homozygous	54093388
7	124355239	124355240	C	T	16	GENIC	possibly homozygous	54093390
7	124356351	124356352	C	A	25	GENIC	homozygous	54093392