chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40701522	40701523	A	-	20	GENIC	homozygous	51426315
10	40702944	40702945	C	CTTCCT	11	GENIC	homozygous	51426323
10	40706674	40706676	TG	--	19	GENIC	heterozygous	52647731
10	40710612	40710616	CTTC	----	8	GENIC	homozygous	52370381
10	40713206	40713207	T	C	13	GENIC	homozygous	51426385
10	40720917	40720918	T	C	21	GENIC	homozygous	51426416
10	40744507	40744508	A	ATGTG	9	GENIC	homozygous	51426502
10	40746144	40746145	T	-	18	GENIC	heterozygous	52438293
10	40746558	40746559	C	CA	28	GENIC	homozygous	51426517
10	40746568	40746569	T	-	25	GENIC	homozygous	51426519
10	40751028	40751032	GTAT	----	19	GENIC	homozygous	51861520
10	40755722	40755723	T	TAG	6	GENIC	heterozygous	52370387
10	40756641	40756642	G	GGCAT	23	GENIC	homozygous	52316629
10	40770933	40770935	GT	--	25	GENIC	heterozygous	52647734
10	40771137	40771138	C	T	26	GENIC	homozygous	51426607
10	40771143	40771144	A	G	27	GENIC	homozygous	51426608
10	40771151	40771152	C	G	24	GENIC	homozygous	51426609
10	40771163	40771164	C	G	27	GENIC	homozygous	51426610
10	40771176	40771177	C	A	26	GENIC	homozygous	52316633
10	40771178	40771179	A	G	26	GENIC	homozygous	52316634
10	40771192	40771193	G	A	28	GENIC	homozygous	52316636
10	40771193	40771194	A	G	29	GENIC	homozygous	52316638
10	40771263	40771264	C	CTA	3	GENIC	homozygous	52370389
10	40771264	40771265	C	CTGTTCTCCTTGTAACTTAGGATAATAGCCGGCTTCTAGTGGGAACTAGT	1	GENIC	homozygous	52494796
10	40775742	40775743	T	TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC	8	GENIC	homozygous	52370393
10	40779474	40779475	T	-	16	GENIC	homozygous	51426641
10	40779475	40779476	C	G	16	GENIC	homozygous	52316639