chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	40944157	40944158	A	-	5	GENIC	heterozygous	53550315
8	40944179	40944183	TCGT	----	20	GENIC	heterozygous	53428293
8	40944463	40944464	A	AT	225	GENIC	heterozygous	53428295
8	40944715	40944716	G	-	136	GENIC	heterozygous	53378819
8	40944835	40944836	C	-	72	GENIC	heterozygous	53378820
8	40945377	40945378	T	TG	112	GENIC	heterozygous	53378822
8	40947731	40947732	C	-	95	GENIC	heterozygous	53378823
8	40948264	40948265	T	-	131	GENIC	heterozygous	53378825
8	40949767	40949769	AG	--	57	GENIC	heterozygous	53550317
8	40949849	40949851	AA	--	20	GENIC	heterozygous	53550318
8	40949850	40949851	A	-	20	GENIC	heterozygous	53550319
8	40950436	40950437	A	-	21	GENIC	heterozygous	52595218
8	40957949	40957950	G	GCTT	25	GENIC	heterozygous	53363264
8	40958441	40958442	T	-	48	GENIC	possibly homozygous	53378826
8	40958524	40958525	C	-	18	GENIC	heterozygous	52595250
8	40963282	40963283	T	-	21	GENIC	heterozygous	53378827
8	40963477	40963478	C	CT	26	GENIC	heterozygous	53378829
8	40963805	40963806	C	CTTT	12	GENIC	heterozygous	53378830
8	40963806	40963808	TT	--	12	GENIC	heterozygous	53428299
8	40965339	40965340	A	-	7	GENIC	heterozygous	53633434
8	40965397	40965398	C	CA	8	GENIC	heterozygous	53428301
8	40965398	40965400	AA	--	8	GENIC	heterozygous	53550321
8	40966298	40966301	CTT	---	57	GENIC	heterozygous	52965091
8	40968404	40968405	A	-	20	GENIC	homozygous	53378832
8	40968672	40968673	C	-	35	GENIC	heterozygous	53428305
8	40969556	40969557	T	-	161	GENIC	heterozygous	53550323
8	40969985	40969986	G	-	80	GENIC	heterozygous	53378833
8	40970260	40970261	G	GCAAGGA	11	GENIC	heterozygous	53378834
8	40976084	40976085	T	-	101	GENIC	heterozygous	52595390
8	40980808	40980809	C	CAT	16	GENIC	heterozygous	53378836
8	40982132	40982136	TGAT	----	40	GENIC	heterozygous	53378839
8	40982468	40982471	AAC	---	8	GENIC	heterozygous	52595410