iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

ATG16L2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs557682996	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823938	TTGGAGAAGTCAAGT[G/T]CTTATCCCAGACTTG	89849
rs557753385	in-del	-/T			intron-variant	ATG16L2	GRCh38.p7	11:72835748	TATACTGGAACATAT[-/T]TTTTTTTTTTTTTTT	89849
rs557811644	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72826071	AACCTGGGGATGTGT[C/T]GGGGGGTGGGGCGGG	89849
rs557934736	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72825422	AGTAAGGAGCCCTCC[C/G]CTGCCGGCCAACTTG	89849
rs558092090	snp	C/T	1.70217e-05	0.00291729	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826477	CCCGAAGAATGTTGC[C/T]TCCGGCTTAGCACCT	89849
rs558203295	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814241	GGACGGGGCCCCGGC[C/G]GTTCAGACCCGGAGG	89849
rs558234726	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72829100	CTCCACCTTCCACCC[A/G]ACCAGAGCCCTTTGC	89849
rs558310810	in-del	-/T	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72834755	CCTGGCTAATTTTTG[-/T]TATTTTTAGTAAGAG	89849
rs558667037	snp	A/G	0.00636936	0.0560724	intron-variant	ATG16L2	GRCh38.p7	11:72816946	TGGCTGCTGCCCAGG[A/G]GTGGTGGGGGTGGTG	89849
rs558728285	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817440	TGGCCAGGATGGTCT[C/T]GATCTCTTGATCTTG	89849
rs558829700	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830599	CTGGTCTTCCCGAAG[G/T]GCTGGGATTACAGGT	89849
rs558866186	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819827	CTCGGCTCGCTGCAA[C/G]CTCAGCCTCCCGGGT	89849
rs558993125	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72830045	CACAGGGCCTCCCTT[A/G]GACTGGGTCCGCGTT	89849
rs559053143	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824636	TTCTGCCGCCTGCCA[C/T]GTCTGCTTCCTATGG	89849
rs559056913	snp	A/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72825773	AGCTCTCAGAACTCA[A/G]GTAAGAGACAAGTAT	89849
rs559077590	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839062	GTTGTTCTCAATGAA[A/G]TATCAAGCCCACAAA	89849
rs559090566	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814401	GCCCCGGCCTGGCGC[A/C]GTCCTGGGCGGGAGG	89849
rs559329195	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832435	GAAACAGGCCAAGGA[A/G]TTCCCGGGAATGAGG	89849
rs559391484	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826304	CTCCACACTGGGCAG[A/G]TGGGGGCTGTGGGAC	89849
rs559418791	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843083	TTATCCTACTGAAGG[C/G]TTACTCCAGGGCAAT	89849
rs559587295	snp	A/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72833571	TTCTATGCGCAGTGT[A/G]GAAGGGCTGTGAGCC	89849
rs559805099	snp	A/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72834875	CAGGCGTAAGCCACC[A/G]TGCCCAGCCATCATT	89849
rs560116965	snp	A/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72830296	ACTCCCAGACCACTC[A/G]CTACTTTTGGTCTAG	89849
rs560134090	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72816080	GCCTCCCAAGTTCAC[A/G]CCTGTCTCCCGTCTC	89849
rs560337744	snp	G/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815832	CTCCCCTGGAACTGG[G/T]GAGAAAAGAGGAAGT	89849
rs560366705	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812982	GTGTGATAACTGGTG[A/T]CGGTTATAACTCGAA	89849
rs560389568	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830752	CCCTTTGGATGTGAC[C/T]CTGCTGGCCTCTCAG	89849
rs560466511	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825201	GAGATACCACGTCTG[C/T]AGCAGGCTGTGTCTG	89849
rs560472705	snp	C/T			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836626	GGATTAATTTACTTT[C/T]TCCTCTCTCTGTCTG	89849
rs560682033	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813664	AGCTCGTTCTCTCCT[A/C]CCGGCCAGGGGCTTT	89849
rs560687008	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815148	ATGCTGGCTGAGCCC[A/G]GCGAAGTCGGACTCT	89849
rs560782632	snp	A/G	1.7894e-05	0.0029911	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840990	AAAGAAGCTCATTTT[A/G]CTTGAGTTGTTGAGC	89849
rs560792460	in-del	-/AAAC	0.00159617	0.0282053	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837231	GTTAAGAAGTGTAAA[-/AAAC]AACAACGAAAAAAAA	89849
rs560893789	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72816506	CAGGTCCTCTTCCAC[G/T]TGGGCCTGGGGACCG	89849
rs561038009	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823174	CAACCCCTACCCTCA[A/G]CCCTTTCCCTCCTTC	89849
rs561073643	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72834659	ATGATCTTGGCTCAC[C/T]GCAACCTCTGCCTCC	89849
rs561110630	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823956	TATCCCAGACTTGAG[A/C]GGTTACAAGCCTCCA	89849
rs561156974	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837009	AATAACCCTTTGAGG[C/T]TGTGGAAAACCCAAA	89849
rs561223655	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817674	GGCTCTTGTTTTAGG[C/T]TTTTCATGTAGCATC	89849
rs561253880	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72836136	CTTACTGCATGTCCC[C/T]AGCTCCAGGAAAGAG	89849
rs561371801	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830910	GCTGGGCCTATAGGT[A/G]CATGCCACCGTGCCT	89849
rs561413558	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837874	AAAATAATGCCGGGG[C/T]GTCCCCAGTAGAGAA	89849
rs561438122	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831559	TCTAACGGTCTAAGA[G/T]CCTTGGGCTCCAACA	89849
rs561448267	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825678	TTGGTGGGGGTCCCC[G/T]ATCATGAGGTCCTAC	89849
rs561499113	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817136	TTTTTCCATTTCCCT[A/G]TTCCTTGCCTGATGC	89849
rs561696549	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819988	CTGACCTCGTGATCC[A/G]CCCACCTTGGCCTCC	89849
rs561699506	in-del	-/GG	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72836162	AAGAGGAGAGCTTGT[-/GG]GGCCCTTCCCCAAAC	89849
rs561821745	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813951	GCTTCCTTATCTTGC[A/T]GTCCTGCTGCGCCGC	89849
rs561984740	snp	G/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827541	ACCAAGATGGAGATG[G/T]ACCTTTTTCCATTTA	89849
rs561993110	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820845	CCTGCTTGGCTCTGG[A/G]TTGAAGGCATGACGA	89849
rs562042315	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820595	AAAGGTGCCCCAACC[C/T]GCATGTGCAGATTCC	89849
rs562052642	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814265	CCGGAGGCGGCTCCT[A/C]CCGGAGGCAGATCCT	89849
rs562229425	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841979	CTGACTTCCCCAGGT[A/T]TTGTGCATGTTAGGC	89849
rs562357912	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826914	TGCTCTCTGGGAGTG[A/G]CTCTGAGATTCATAG	89849
rs562368470	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827512	CCAATGCTGGACTCC[A/G]CCTGGACCTTGCAAC	89849
rs562399743	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823477	GTCTCCTCCATCCTT[C/T]TTGATTTGCCTGTCA	89849
rs562496673	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72819952	GGGTTTCACCATGTT[A/G]GCTAGGATGGTTTTG	89849
rs562569534	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838109	TGGCTACTAGTTCAG[C/G]CCCTCCATATTAGCT	89849
rs562760783	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829505	GATTTAATGGGGAAG[A/G]AGGCCTGGCAGGACC	89849
rs562772338	snp	C/T	3.29592e-05	0.00405938	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824154	CTGTGTGTGCACCCA[C/T]GTGTGTGTCGGGCTC	89849
rs562843635	snp	A/C/G	8.28365e-05	0.00643526	synonymous-codon, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824758	GAGGAGAGGTCACTC[A/C/G]ATTGGGGGAGCCCCT	89849
rs562856542	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841666	ACTGCTCTGTACTCA[C/T]GCCTTTTCTCTAAAG	89849
rs562863097	snp	C/T	0.000568801	0.0168546	intron-variant	ATG16L2	GRCh38.p7	11:72817919	GGAGCCAGCCAGTGA[C/T]GGGTACTCCTGTGTT	89849
rs563052633	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839688	GGGAGAAGGAACATG[C/T]CTGGAAGGGAACATA	89849
rs563103397	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815929	GCTCAAGGACTTTCT[A/G]TTCTGGCCTGGGGGT	89849
rs563269035	snp	A/C/T	8.19462e-05	0.0064006	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826857	CCCACCTCTCCTCCC[A/C/T]ACCAGCCAGGAGCCC	89849
rs563440636	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827655	GTAAAAGCAAAGCTA[C/G]AGGCCAGGCGTGGTG	89849
rs563451221	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828135	CCAAAGGTTTCAAAG[A/G]CTCCAGCTTTCAAAT	89849
rs563621415	snp	A/C/G	0.000462897	0.0152069	missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843170	GGCATCTCCGTTGAG[A/C/G]CTGCCTGAAACGAGT	89849
rs563837940	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839485	AATCCTCTGAATGAG[A/C]GTTGACAATAGCCCA	89849
rs563910269	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815110	GCCTGAGGGGGCATC[A/C]GGGGGCCCCGGGCTG	89849
rs563936338	snp	A/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824238	TGCAGCTGTCTGCCT[A/G]TGAGTCTGTTGGGCC	89849
rs563995514	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816526	CCTGGGGACCGGTGC[C/T]ATGAGGACACTGCTA	89849
rs564000672	snp	A/C			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814878	TCTCTTTTGCCTCCC[A/C]ACCCGGGCAGTCCCC	89849
rs564088439	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72833904	CTCCAGCCTGGGTGA[C/T]GAGCGAAACTCCGTC	89849
rs564099987	snp	A/G	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72825230	TGCACAGGCACCGGT[A/G]AGAGGGCCCGTGAGC	89849
rs564209944	snp	C/T	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72819577	GCCTGGCTCCCCCGT[C/T]GAGCTCCCCAGGCTC	89849
rs564389647	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825603	GGTGGAGCCTCCTGG[C/T]TCCTAGGGTCCAGAT	89849
rs564413760	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813098	CCAGGCCCCCTAGAG[A/G]CGACGATGTTCCAAA	89849
rs564426238	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813828	GCACGTGCTCTTCTC[A/G]AGGCCTAGAGTCCCT	89849
rs564452467	snp	G/T	0.00199481	0.0315187	intron-variant	ATG16L2	GRCh38.p7	11:72819907	CCCGCCACCATGCCC[G/T]GCTAATTTTTTGTAT	89849
rs564637547	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826327	TGTGGGACCTGAGGG[C/T]GCAACATGGATACCC	89849
rs564670288	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840293	ATGAAGCCAAAAGAA[A/G]CCAGTGGTAAAGGAA	89849
rs565173024	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837265	CCCCAAATCATGGAG[A/G]AGATTCATTAATGGG	89849
rs565185548	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838069	CACAGCCTCCTTTCT[A/G]TTAGTCTATGTGATG	89849
rs565192203	snp	A/C	1.64751e-05	0.00287007	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828774	GACCAAAGCTGTGTT[A/C]AGGTATGTCCGTGAG	89849
rs565219118	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824036	AGCCAGTCCCTTAGC[A/G]TATCTCTCTTGGTTT	89849
rs565419706	snp	C/G	0.0023933	0.0345097	intron-variant	ATG16L2	GRCh38.p7	11:72820034	ACAGGCGTGAGCCAC[C/G]GCACCCGGCCTTTTC	89849
rs565619755	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813388	GCCTGCTGGCATGCC[C/G]CAGGGTGAGGCTGTG	89849
rs565661698	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841394	TTTTTGCCCTTCAGG[C/T]GAATATGTAGGTTTC	89849
rs565731540	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72835681	AATCTAACAAAATTA[A/C]ATACATACCTTTTTG	89849
rs566047039	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826963	TCTCAAGGCCCTCCA[A/G]TTCCCTAATGGTATC	89849
rs566160132	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826461	TAGCCTCATTCTGTG[A/G]CCCGAAGAATGTTGC	89849
rs566187431	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821201	CTTGTCTGTGAAGTG[A/G]GAGTGGCAGTACCAG	89849
rs566246310	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821812	CAACTATACGGGAGG[C/G]GGGGGGAATGGCGCG	89849
rs566248213	snp	C/T	4.61627e-05	0.00480409	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814569	GTGCCGGCCTGTGAG[C/T]GCGCCCCGGTGCTGA	89849
rs566495285	snp	C/T	1.6483e-05	0.00287076	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828473	CACACTCAAGGTCAT[C/T]GACCTGCGTGTCAGC	89849
rs566578531	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829559	GTATGGGTTGGGGGA[C/T]TACGCTAGTTTTTCT	89849
rs566589206	snp	A/G	0.000339501	0.0130244	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823771	CTCCCTGTAGGCCCC[A/G]GCTCAGCTTCCCAGG	89849
rs566591222	snp	A/G			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828028	TACTCACTGATCTCC[A/G]GCAATTACTGTTTGC	89849
rs566657034	snp	A/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72817366	TCAGCCTCCTGGAAC[A/G]TGCACCACCACCCCC	89849
rs566703479	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824205	TGTCTGTGCCTCGAC[C/G]TGTCCATCCCTGTGA	89849
rs566703646	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72817371	CTCCTGGAACGTGCA[C/T]CACCACCCCCGGCTA	89849
rs566914526	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838406	GATGAGAATCTTTGC[C/T]ACATCCTTGTGGTCA	89849
rs567149905	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831005	CTTCCCTCCCAGCCC[C/T]CAGTTCAAATTTTTC	89849
rs567353475	snp	A/C	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822707	GTGTGGTCGTAGGAG[A/C]CTGCATGCGTGACCG	89849
rs567402996	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72835124	AAATTTAGCTATGAC[A/G]CTGGGGTGAGGCAGT	89849
rs567494917	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834111	ACAGGAAGAGTCTAG[A/G]AGGAAACTTAAAAGT	89849
rs567610776	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72826058	GATTCTGTCTTCTAA[C/T]CTGGGGATGTGTCGG	89849
rs567658642	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816615	CTGCCAGAAGCTTCC[C/T]CATCCCTAGCATCTC	89849
rs567673408	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813439	GTGTCTCACAGTAGC[C/T]TGAGCCTGCAGAGCT	89849
rs567709163	snp	C/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821458	GCGAGGATTGGGACC[C/G]AGGGCTGACTCCAGA	89849
rs567741766	snp	C/T	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816220	CTCCTGACCTCGTGA[C/T]CCGCCCGCCTCGGCC	89849
rs567745371	snp	C/G	7.48629e-05	0.00611767	intron-variant	ATG16L2	GRCh38.p7	11:72824854	GCTGGTAAGGGAGGA[C/G]CTGAGCCACATGGGT	89849
rs568073017	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812569	TATTTATTTAACATT[A/T]CCTAGGTGTATTTTG	89849
rs568342491	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840099	CTCCAGCCTCCTAAT[C/T]GCTCCCTATATCCTT	89849
rs568480826	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840651	AGCCATCATCTTGCA[A/T]TCTCACTGTGGCTCA	89849
rs568496647	snp	A/G	0.0023933	0.0345097	intron-variant	ATG16L2	GRCh38.p7	11:72831976	CCTGCCTGCTACCAC[A/G]GGGGTAGAGGTGTGA	89849
rs568508727	snp	A/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843138	ATAAAGAGTGCCTTG[A/T]TTCAGTCTTTACCAC	89849
rs568533603	snp	C/T	0.00478085	0.0486577	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72816244	CTCGGCCTCCCAGAG[C/T]GCTGGGAATTCAGGT	89849
rs568598463	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813353	GGGATGTTCAAGTCT[A/G]CCAACACTCAGAGGG	89849
rs568656095	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814079	CTCGAACTCGGCCCG[A/G]GCGCGGCGGGGTTAA	89849
rs568701370	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826398	TGGGCCGGAGGCTCC[G/T]TTGCCTGCCTTGGTG	89849
rs568739118	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814471	CGGGCGTCCCCGGTG[C/G]CCCCGCAGCGCGCTG	89849
rs568759470	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827758	AGCCTAGCCAACATG[A/G]CGAAACCCTGTCTCT	89849
rs568762255	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821150	CTCTTAGCTACGTGA[C/T]TTTGGGCAAGACACT	89849
rs568829417	snp	C/T	0.0123036	0.0774623	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823292	CATGCCAGGCATGTG[C/T]GCGCAGCCATAGGTG	89849
rs568895426	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72825231	GCACAGGCACCGGTA[A/G]GAGGGCCCGTGAGCA	89849
rs568909857	snp	A/C	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72835451	GGAGAGGTGGTGGTG[A/C]GAAGAGTTCGTGGTG	89849
rs568923835	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836297	ACACAATTCATTACT[C/G]CTTAGGGTGGAGGTT	89849
rs569044678	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823513	GCTGCCCGCTCTGGG[C/T]GCCATTCCCCAGCCT	89849
rs569090223	snp	A/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72816270	CAGGTGTGAGCCACC[A/G]CGCCCGGCTGGGGAT	89849
rs569100498	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72828836	GGACCCTGTGTGTGC[C/G]CTCCCCTCTGACCCC	89849
rs569123429	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816789	GAAGCTGCAGCCGGA[A/G]CCAAACAGTGTCACT	89849
rs569163496	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829798	CAAGTCTAACCATGG[A/G]AACAGCAGGAAGAAA	89849
rs569205339	snp	A/G			upstream-variant-2KB, intron-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812408	CAGCAAGTTAAATGT[A/G]AAAAGCAGAAATTTG	89849
rs569222004	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830488	GCCAGAGTGACTTTT[G/T]TTGTTGTTGTTGTTG	89849
rs569226414	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824577	ACCAACCCCTGGGGT[C/T]GAGGCTGGGTTGGGG	89849
rs569274159	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814057	GGCCTGGGAAGCACC[A/T]GCGGCTCTCGAACTC	89849
rs569279274	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72820245	CAACCAGGAAACTGG[G/T]ATTGGTATGAAGTGT	89849
rs569629681	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72833750	ACATGGTGAAACCCC[A/G]TTTCTACTAAAAATA	89849
rs569805158	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842282	CTAAGAGTTTTACTA[C/T]GTAAATTAACCACAG	89849
rs569813321	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813501	ACCACAGTTCCCTGC[A/G]ACCCATGATTCACTT	89849
rs569820643	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72817189	TGTTGCAAAGAGGGA[A/G]TAAAGATGAGAACCA	89849
rs570015619	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839367	GTTTTTGGTGGATTT[G/T]AAGCAATATCAGATC	89849
rs570031472	snp	C/G			missense, synonymous-codon, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842629	CAGGTACCTGAATCT[C/G]TCTCATCCATGGAGT	89849
rs570125250	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816123	AGCTGGGACTACAGG[C/T]GCCTGCCACCACGCC	89849
rs570134585	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815445	AGCAGCCACACTTCT[A/C]CACTGCTCAGACAGA	89849
rs570389066	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829651	CTGCGTCTGCCTACC[A/T]CTTTGCAGCATTCAT	89849
rs570589661	in-del	-/AT	0.00438332	0.0466095	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836470	CCTCCCTTCTAGCAC[-/AT]GTCCCACAGTACTGT	89849
rs570898083	snp	C/G/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839132	TCCTATGACTAAGAT[C/G/T]CTAGCACATCCTCCA	89849
rs570981401	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831171	CCTGGGATCAGGCCT[G/T]GCACAGAGAATGACT	89849
rs571004799	snp	C/T	0.00557542	0.0525036	intron-variant	ATG16L2	GRCh38.p7	11:72818773	GCTATATCCAAAGTA[C/T]GGGGAGTGCAACAAT	89849
rs571057533	snp	A/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819831	GCTCGCTGCAACCTC[A/T]GCCTCCCGGGTTCAC	89849
rs571092794	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831927	GTTAGGCAGGGCTGC[A/G]GGGCATGCCCCCTCC	89849
rs571121697	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825927	GTGCTCTACATAGTC[C/G]CTTCTCCCTGGTCCT	89849
rs571135424	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72820047	ACGGCACCCGGCCTT[C/T]TCTTTTCTTTTGTAA	89849
rs571195619	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837888	GCGTCCCCAGTAGAG[A/C]AGCTCAACAATGCAG	89849
rs571279922	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816654	TTCAGCCCTTTTAGC[C/T]GGAGATAAATTGCAT	89849
rs571390562	snp	G/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72817253	TTGCTTTTTTTTTTT[G/T]GAGACGGAGTCTGGC	89849
rs571455963	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827858	GAATGGCTTGAACCC[G/T]GGAGGCAGAGGTTGC	89849
rs571460246	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823206	TGGGATCAGAGCTCT[A/G]GGGGTGGGGAGTCAG	89849
rs571497946	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72836241	TCAGCCTTTGACTAA[C/G]AATGCTCCATCCACC	89849
rs571517082	snp	G/T	0.000102717	0.00716574	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822802	CTGGGGTCGGGAGGG[G/T]CTGGCTTGGTCCCTT	89849
rs571560176	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835242	ATTTCGTGTCCTGAC[A/G]GCCCTTCCCACATTT	89849
rs571630857	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838278	CTTTCTCAGTCTGGG[A/G]ACTAACCTTGGGGAG	89849
rs571896294	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839459	AAGAAGGCAACTTAG[A/G]AGACTTTTGTAATCC	89849
rs571959634	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840262	AGAAGGCACTCAATA[C/T]ATATTTGCTGAATGA	89849
rs572055260	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837061	TAAAGACAGAATACA[A/G]GACTGGGTGGCAAGA	89849
rs572165179	in-del	-/G			intron-variant	ATG16L2	GRCh38.p7	11:72832715	CTGAGACCCAGAGAT[-/G]GGGCAGCTCCTTCGG	89849
rs572197238	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72830769	TGCTGGCCTCTCAGC[C/T]TCATCTTCATTTCCT	89849
rs572207448	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825222	GCTGTGTCTGCACAG[G/T]CACCGGTAAGAGGGC	89849
rs572563474	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813711	GCACCCCTTTACTCT[C/G]AGGGACCTAAAATTT	89849
rs572567836	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72820448	TACTTGAATTTTGAA[A/G]GGCATACAATAAAAT	89849
rs572581900	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814101	CGGGGTTAAGACACC[C/T]GGGCCTTGAGGGCCC	89849
rs572907523	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823043	CCTCTTGGACCTTGG[A/G]GCCAGCTCTTGGGTT	89849
rs572970418	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823294	TGCCAGGCATGTGTG[C/T]GCAGCCATAGGTGTG	89849
rs573021635	snp	C/T	6.58968e-05	0.00573969	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824029	ACACACCAGCCAGTC[C/T]CTTAGCATATCTCTC	89849
rs573135338	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824623	CCTTGGGGCCATGTT[A/C]TGCCGCCTGCCATGT	89849
rs573135418	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817676	CTCTTGTTTTAGGCT[C/T]TTCATGTAGCATCAC	89849
rs573200937	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837839	CCTGGCTGTCTGGGC[C/T]GGTCTGCTGGCTTGG	89849
rs573215028	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72829238	AGGTCCAGCAGTCGG[A/G]GCAGAGCCAGGTTGC	89849
rs573305762	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829891	GCAACATGTTGGGCC[C/T]ACCTGCTTCAGGCAC	89849
rs573423104	snp	C/T	1.84228e-05	0.00303497	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826281	CATGGGATTGTGCCC[C/T]CTCTGATCTCCACAC	89849
rs573456440	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72825808	TGTTGGCCTTGTCCC[A/G]AGCTCTGTGCTCTGG	89849
rs573533915	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823279	CCCAGAGCCCAGTCA[C/T]GCCAGGCATGTGTGC	89849
rs573541908	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840483	GGAGAATAAACGCTC[C/T]TTAAGGCCATGAAGT	89849
rs573554911	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821366	CGCTGGCTTCCCACT[C/T]TTCAGGCGAGGCAGT	89849
rs573734222	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72833127	CTTCAGTCTGCTGTT[A/G]CGCTGAGTGTCTCCC	89849
rs573883375	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843016	ACTGTGCAGGACAAA[C/T]GTGACCATATAAAGA	89849
rs573953634	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823763	CGTCTCTCCTCCCTG[C/T]AGGCCCCGGCTCAGC	89849
rs573980900	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815682	GGTTTGCTGGGTGCT[A/G]CAGTACCCTGGGGGC	89849
rs574209789	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72835752	ACTGGAACATATTTT[G/T]TTTTTTTTTTTTTGA	89849
rs574265065	snp	A/C			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826340	GGCGCAACATGGATA[A/C]CCTAGAACCAGGCCC	89849
rs574370665	in-del	-/T	0.00159617	0.0282053	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839543	AGAGAAGTGGAAAGA[-/T]TTGCGAGCTCTCTGC	89849
rs574549620	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838544	GGCTGCCCCCCTCTT[G/T]GCTCCTAGGGTCCGC	89849
rs574642742	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839338	CTGTGCTTTATTCTG[C/T]AGGCAAAAGAGGAGT	89849
rs574751759	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72830113	AGGCCTCTGTGTGTC[C/T]GTGCCTGGGGGAGGG	89849
rs574795515	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819285	TCTCCAAATCCATCA[A/G]TGTCTCTCTGTTTCT	89849
rs574855701	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812944	GGTCCTGCCCTAAGG[G/T]GCACCGCACAGATTA	89849
rs574865007	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830659	GACTTTCTAGGGTGT[C/T]GTGTTCACAAGTCCA	89849
rs574893250	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819865	ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG	89849
rs575011142	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813566	CAGACGCCGCCCAAT[C/G]GGGTGAAGCGTCTGG	89849
rs575287927	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72834428	AGTCCAGTGGCTTGC[C/T]TTCTTTTCAATTTCT	89849
rs575361579	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827907	CACTGCCGTCCAGCC[A/T]GGGCGACAGAGCGAG	89849
rs575414420	snp	A/C	0.00279162	0.0372561	intron-variant	ATG16L2	GRCh38.p7	11:72828620	CCCTCCAGACCAGGT[A/C]CTGCTGAGGTACCAA	89849
rs575476192	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72829198	AGATGAGGAAACAGG[C/T]TCAAGAGAGGGCCTC	89849
rs575486677	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823939	TGGAGAAGTCAAGTT[C/T]TTATCCCAGACTTGA	89849
rs575616958	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836932	GTTTTCACAACTTTG[C/T]TTTTTAAAATAAAAT	89849
rs575695550	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840334	AGCTAATAGGGGTCA[A/G]GGAAAATAAAATTGC	89849
rs575779454	snp	G/T	0.00318978	0.0398085	intron-variant	ATG16L2	GRCh38.p7	11:72818920	GGTACGGACTCATTT[G/T]AGAACCTTTCCCTAG	89849
rs575807193	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831545	AAGGACTCAGCCAGT[C/G]TAACGGTCTAAGAGC	89849
rs575863435	snp	A/G	0.00438332	0.0466095	intron-variant	ATG16L2	GRCh38.p7	11:72817585	AGCAGAGGAGTCATG[A/G]ACAGCTCATTTCTAG	89849
rs575870939	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832283	CTTCTACTTTATGGG[C/T]GTCAATCTTACCACA	89849
rs575993117	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841159	GGTGACAGAATAATA[C/T]CCTTTGTCCAGAAAA	89849
rs576011832	snp	C/T	0.00358779	0.0422022	intron-variant	ATG16L2	GRCh38.p7	11:72835092	CATCAAGTCAGTTCC[C/T]GTGATGAAGGAGACC	89849
rs576197786	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825626	GTCCAGATTTGCAGG[A/G]TGGGGAGGGCTGAGT	89849
rs576236787	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72826077	GGGATGTGTCGGGGG[G/T]TGGGGCGGGAACTGA	89849
rs576384327	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821300	ATGGGCATTTGGCAG[C/T]CTCTGCGCGAGGAGT	89849
rs576447825	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814729	ACTCCGCCCCTTGCC[A/G]TCCAGGCTCTGGTTA	89849
rs576505585	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72836071	TTTTATGTAAACAAG[A/C]AGTGTGTACACTTAA	89849
rs576533444	snp	A/C	0.00517822	0.0506191	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814249	CCCCGGCGGTTCAGA[A/C]CCGGAGGCGGCTCCT	89849
rs576579386	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841815	ACTGATTTTAGTTTA[A/T]CTTAAACAGTTATCA	89849
rs576622316	snp	C/T	5.63037e-05	0.00530553	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842886	AAGATAATTAACAGC[C/T]GGTTGCTTTTGCAAC	89849
rs576778495	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72833315	GGCTCTTCCACTGGA[A/G]ACACATTCACTCATC	89849
rs576911712	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824349	GTCTTCATCCAAGGT[C/T]GTCACAGGGGACCAA	89849
rs576950679	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816954	GCCCAGGGGTGGTGG[A/G]GGTGGTGGAGGTGGT	89849
rs577011578	snp	C/G	0.0023933	0.0345097	intron-variant	ATG16L2	GRCh38.p7	11:72817441	GGCCAGGATGGTCTC[C/G]ATCTCTTGATCTTGT	89849
rs577120312	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812775	AGGGAATTCATCACT[C/G]TCATCAGCTGGCCCT	89849
rs577120483	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813443	CTCACAGTAGCCTGA[A/G]CCTGCAGAGCTGGCT	89849
rs577174857	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838075	CTCCTTTCTATTAGT[C/T]TATGTGATGAACAAG	89849
rs577218554	snp	A/G	1.65776e-05	0.00287898	intron-variant, synonymous-codon	ATG16L2	GRCh38.p7	11:72824699	TGAGAAGGACTTGCT[A/G]AATGCCCTCCTGACC	89849
rs577282538	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825146	ACACCTGGTGGGGCC[A/G]GGTTTGAAACTCAGA	89849
rs577287749	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838534	TAGGCATGAGGGCTG[C/T]CCCCCTCTTTGCTCC	89849
rs577351604	snp	C/T	0.00279162	0.0372561	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72830057	CTTAGACTGGGTCCG[C/T]GTTCTTCCTCCAGGG	89849
rs577363586	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830617	TGGGATTACAGGTGC[A/G]CAGCACCATGCTCGG	89849
rs577394506	snp	A/G/T	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72819183	GACTGCCCCCCAGTC[A/G/T]TTCTCACACATGCTG	89849
rs577550172	snp	A/G	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72832510	GAGGGGCATGTCAGC[A/G]GGAAGGCTGTTCCTC	89849
rs577795525	snp	C/G	0.00149078	0.0272611	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822420	AAGGGACCGGGTCTA[C/G]CCCCGCCTGCGTGCG	89849
rs577864620	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836732	ACCTTTCTATATTAA[A/C]ACTTAGAAAACATAA	89849
rs577869126	in-del	-/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837841	GGCTGTCTGGGCCGG[-/T]TCTGCTGGCTTGGGA	89849
rs577890569	snp	A/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839707	GAAGGGAACATAACT[A/C]ATTTTTGCTGAGTTT	89849
rs577942206	snp	C/T	0.000115953	0.00761333	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828326	GGCCTGGCTAGGCTG[C/T]TCCTCATCCCTGTCT	89849
rs578127977	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72832319	TGCTGCCATCGGGTG[C/G]AGTTGCCTCTCTCAG	89849
rs578153401	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72827968	AAAAACAAAACAAAA[C/T]AAAAAAACAAAGCTA	89849
rs578204863	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823324	GCAAGCATGTGCATC[C/T]GCAGGGACATGAGGC	89849
rs578235448	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813649	AACCCCAGGCAAGCA[A/G]GCTCGTTCTCTCCTC	89849
rs745310383	snp	C/G/T	0.000162995	0.00902633	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838917	TCAGTCAGTTCCTGA[C/G/T]TCAGTATCTGAAGCA	89849
rs745347007	snp	A/G	0.000105446	0.00726031	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823497	TTTGCCTGTCATTGA[A/G]GCTGCCCGCTCTGGG	89849
rs745478603	snp	C/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813185	ACTGAGCCCAGCTCA[C/G]TGGAAGCAGAGCAGG	89849
rs745505072	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841765	CCAATTTTGCATTGC[A/G]CTTCACTTTTTCCTC	89849
rs745524855	snp	C/T	1.6585e-05	0.00287962	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840903	TGCCATATGAGGTCT[C/T]AGGAGTATGCCTTGA	89849
rs745556164	snp	C/T	1.90514e-05	0.00308632	intron-variant	ATG16L2	GRCh38.p7	11:72824863	GGAGGAGCTGAGCCA[C/T]ATGGGTGGGGCAGTG	89849
rs745615608	snp	C/T	1.64749e-05	0.00287005	intron-variant	ATG16L2	GRCh38.p7	11:72828796	GTCCGTGAGAGCATA[C/T]GCCTGTGTCCAAGTG	89849
rs745685749	snp	A/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839572	GCAAGGTATACCTGG[A/C]AGGATTTGGGAATGA	89849
rs745798505	snp	A/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823307	TGCGCAGCCATAGGT[A/G]TGCAAGCATGTGCAT	89849
rs745808792	snp	A/C/G	9.33576e-05	0.00683155	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822087	CAGCTGCGAGAGGCG[A/C/G]GGGCGCAGCAGGCCC	89849
rs745817335	snp	A/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824595	GGCTGGGTTGGGGAA[A/T]GCTCTCGCTGCTCCT	89849
rs745884666	snp	A/G	0.000102202	0.00714778	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822805	GGGTCGGGAGGGGCT[A/G]GCTTGGTCCCTTGGC	89849
rs745912141	snp	C/T	1.68354e-05	0.00290128	synonymous-codon, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829333	CGTGGCCTGGTGCTA[C/T]TCCGGGAGCCACATG	89849
rs745962549	snp	C/T	1.66175e-05	0.00288244	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826783	AGTGACTGGGAGCCG[C/T]GACCGGACAGTGAAG	89849
rs745976106	snp	A/G	1.64738e-05	0.00286995	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824047	TAGCATATCTCTCTT[A/G]GTTTTGTCTCAGGTC	89849
rs746082057	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72831047	CCCTTCCTTCGCCTG[C/T]CAGGCTGGGTAGAGG	89849
rs746106146	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72818151	ACTCCATGGCTCACC[A/C]CTCGCCCAGCCATCC	89849
rs746186522	snp	C/T	0.000100174	0.00707649	intron-variant	ATG16L2	GRCh38.p7	11:72825285	GGCCGGGGCACCAAC[C/T]TCCCCTTTCCCCACA	89849
rs746187247	snp	A/T	1.64784e-05	0.00287035	missense, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842625	CTCTCAGGTACCTGA[A/T]TCTCTCTCATCCATG	89849
rs746210320	snp	G/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827068	TGCTGGGAAGCGGAA[G/T]ACCTGGGTTCTAGTC	89849
rs746248276	snp	A/G	3.48803e-05	0.00417599	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822354	CTGCAGGGAGGAGTC[A/G]GGCCTCGCCGGTGTC	89849
rs746316730	snp	A/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836515	TTTTTTTTCCCATGG[A/G]AAAAGCAAAGACCGT	89849
rs746350119	in-del	-/CTC	1.6834e-05	0.00290116	intron-variant	ATG16L2	GRCh38.p7	11:72825457	TTCTCTCCAGACCCT[-/CTC]CTCAGCTCACTCCTT	89849
rs746426935	snp	C/T	1.66211e-05	0.00288275	intron-variant	ATG16L2	GRCh38.p7	11:72829013	CCACCTGGCCACCTG[C/T]CTGGCCCCAGTCCTG	89849
rs746444521	snp	C/T	1.65921e-05	0.00288024	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822398	GGCAGCAGCCGCCCC[C/T]TGGAGGAAGGGACCG	89849
rs746456952	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837875	AAATAATGCCGGGGC[A/G]TCCCCAGTAGAGAAG	89849
rs746459407	in-del	-/TGCGTTC	2.05821e-05	0.0032079	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822573	GGCCGGTCCGACCCT[-/TGCGTTC]TGCGTTCTGCCTCCC	89849
rs746480218	snp	A/G	1.70035e-05	0.00291572	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822490	AAGGGCCAAGCAGGC[A/G]CGGGTGTCCCAGGAG	89849
rs746495358	snp	C/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823424	TCACACTTGTGGGAC[C/G]TGATTGGGGCTTCAG	89849
rs746527281	snp	A/G	4.70633e-05	0.00485071	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822594	TCTGCCTCCCGCCCC[A/G]CCTGCCTGCGGCGAC	89849
rs746535246	snp	A/C	1.66023e-05	0.00288113	intron-variant	ATG16L2	GRCh38.p7	11:72816700	GGTATCTGTCTCTGC[A/C]CCAGGCTCACTCTCT	89849
rs746711858	snp	C/T	0.000102246	0.0071493	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827148	GGTGGCTCCCGACAA[C/T]CCTCCTCTGAGGCCC	89849
rs746724170	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72833372	TTACCCTATTTCATC[C/T]TCCTGGATCTTAGAA	89849
rs746724931	snp	A/G	1.67301e-05	0.00289219	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838905	TTACGTAGTTTGTCA[A/G]TCAGTTCCTGACTCA	89849
rs746736841	snp	A/G	6.30524e-05	0.00561446	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841472	TTGCTGAAGGAGACC[A/G]GGGAAAGTACAGGGA	89849
rs746748548	snp	C/T	9.68758e-05	0.00695906	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821518	AGCAGCGCGTCCCTG[C/T]GCAAGGTCCCAAACC	89849
rs746843598	snp	C/G	6.58827e-05	0.00573908	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822002	CACTGGGCAGTGACG[C/G]GGGAAGCTTGGGACC	89849
rs746951892	snp	A/T	1.65776e-05	0.00287898	intron-variant	ATG16L2	GRCh38.p7	11:72828550	GTGGCCTTTGCTGGG[A/T]CAGCTGAGCCTCTCT	89849
rs747009341	snp	A/T	4.14938e-05	0.00455469	intron-variant	ATG16L2	GRCh38.p7	11:72826126	AATTCCTCCATTTTG[A/T]GAGGTTAAGACCTCA	89849
rs747046140	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828910	CTATGCACTGGCAGG[C/T]TCCTGTGATGGGGCC	89849
rs747079071	snp	A/G	3.69932e-05	0.00430061	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822335	CTGAGGAAAGGCCCC[A/G]CCCCTGCAGGGAGGA	89849
rs747219538	snp	C/T	0.000148858	0.00862593	intron-variant	ATG16L2	GRCh38.p7	11:72828996	ATTGGTGAGCATGGC[C/T]TCCACCTGGCCACCT	89849
rs747239084	snp	C/T	3.30131e-05	0.00406269	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826662	GGCCTGTTATGGGGT[C/T]TTGGCCAAACTCTTG	89849
rs747319554	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815271	GCGATTGTATGTCTG[C/T]GGTTGGAAGTCTAAC	89849
rs747341716	snp	A/G	1.64811e-05	0.00287059	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827257	ATATCATCATTAGTG[A/G]CCACAATGACCAGAA	89849
rs747394734	snp	C/G	1.8257e-05	0.00302129	splice-donor-variant	ATG16L2	GRCh38.p7	11:72824843	GCTCAGGATGTGCTG[C/G]TAAGGGAGGAGCTGA	89849
rs747409432	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72816276	TGAGCCACCGCGCCC[A/G]GCTGGGGATTATTTT	89849
rs747423081	snp	C/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827116	TCTGGGCCTCAGCTT[C/T]TCCATATGTCCTGTG	89849
rs747465670	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837758	CTTCCTTCCACGGAA[A/G]TGTCAGGGTAGTGGG	89849
rs747497341	snp	G/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839206	AAATGAAACATTTCA[G/T]TGTGTCTTGGGTAGA	89849
rs747510209	snp	A/T	7.97099e-05	0.00631257	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841588	GAAGGAGAGATCTGC[A/T]GCAAAGGGAAGCGAG	89849
rs747525162	snp	A/G	0.000298909	0.0122215	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822137	GGCGCAGAATGCGGT[A/G]CAGCGGGCAGCCTAC	89849
rs747538666	snp	C/T	1.64963e-05	0.00287192	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842609	AATTCAACTGTCTCC[C/T]CTCTCAGGTACCTGA	89849
rs747553851	in-del	-/A	2.4551e-05	0.00350356	frameshift-variant, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838840	CTGCTGGCCTTCGGT[-/A]GATTCTGTGTAGGTG	89849
rs747587070	snp	A/G	3.35284e-05	0.00409427	intron-variant	ATG16L2	GRCh38.p7	11:72825277	GCGGGGAGGGCCGGG[A/G]CACCAACCTCCCCTT	89849
rs747620490	snp	C/G	1.65436e-05	0.00287602	intron-variant	ATG16L2	GRCh38.p7	11:72828540	TGCTGACCCTGTGGC[C/G]TTTGCTGGGACAGCT	89849
rs747675632	snp	C/T	1.68122e-05	0.00289928	intron-variant	ATG16L2	GRCh38.p7	11:72825453	GTGCTTCTCTCCAGA[C/T]CCTCTCCTCAGCTCA	89849
rs747692688	in-del	-/TT			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821151	TCTTAGCTACGTGAC[-/TT]TGGGCAAGACACTTA	89849
rs747728202	in-del	-/TGGGGTCT	1.65046e-05	0.00287264	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826656	CTAGGGGGCCTGTTA[-/TGGGGTCT]TGGCCAAACTCTTGA	89849
rs747768845	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821493	GAGGGCCTTCCACTG[C/T]TCCACAAACAGCAGC	89849
rs747796955	snp	C/G	1.70362e-05	0.00291853	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843141	AAGAGTGCCTTGTTT[C/G]AGTCTTTACCACTGG	89849
rs747889378	snp	C/T	1.71185e-05	0.00292557	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822474	ATGCTTTTTACCCAA[C/T]AAGGGCCAAGCAGGC	89849
rs747912349	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72831235	ATTCAGGCTGGATGC[A/G]GTGGCTCACGCCTGT	89849
rs747967304	snp	A/G	5.18722e-05	0.00509248	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817830	GGCAGGAGGAGGAGG[A/G]GGGGCTCCGGCTGGT	89849
rs747995950	snp	C/G			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829932	CTGAAGCTGAGGAGG[C/G]GCTGGGGGAGCTCTG	89849
rs748017056	snp	C/T	0.000131802	0.00811688	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842763	TCTTTGTTCAAGATA[C/T]GGATTATTGCTCCCT	89849
rs748149896	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72830223	CTTTACCAACCTAGG[A/T]CTGGGCACAGGCCTG	89849
rs748150660	snp	G/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827912	CCGTCCAGCCTGGGC[G/T]ACAGAGCGAGATGTC	89849
rs748161460	snp	A/G/T	0.000208073	0.0101977	intron-variant	ATG16L2	GRCh38.p7	11:72817920	GAGCCAGCCAGTGAC[A/G/T]GGTACTCCTGTGTTT	89849
rs748188568	snp	C/G	4.70267e-05	0.00484883	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841569	GGAGGCGTGTGGCTT[C/G]GGGGAAGGAGAGATC	89849
rs748199017	snp	A/G	0.000339109	0.0130169	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822035	CTATCCGCTCTTTCC[A/G]TCCTCCAGGCTGGCA	89849
rs748213121	snp	G/T	3.60913e-05	0.00424786	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824837	ACCCGGGCTCAGGAT[G/T]TGCTGGTAAGGGAGG	89849
rs748235939	snp	C/G	1.78404e-05	0.00298662	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822101	GCGGGCGCAGCAGGC[C/G]CAGCAGGTGGAGGAG	89849
rs748303731	snp	A/C	1.66957e-05	0.00288922	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842584	GAGCAATTTTCTTTA[A/C]ACATCTTTTAATTCA	89849
rs748358860	snp	A/G	0.000625813	0.0176781	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828886	TGGCCACTACAGCCC[A/G]GACAGAAGCTATGCA	89849
rs748364499	in-del	-/G	7.82167e-05	0.00625318	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822379	GGTGTCTGGAAGGGA[-/G]GGGGGCAGCAGCCGC	89849
rs748384619	snp	C/T	1.64749e-05	0.00287005	intron-variant	ATG16L2	GRCh38.p7	11:72828816	GTGTCCAAGTGTGCC[C/T]TGCCGGACCCTGTGT	89849
rs748417008	snp	C/T	1.88219e-05	0.00306767	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826289	TGTGCCCTCTCTGAT[C/T]TCCACACTGGGCAGG	89849
rs748445392	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839342	GCTTTATTCTGTAGG[C/T]AAAAGAGGAGTTTTT	89849
rs748481468	snp	A/T	3.29728e-05	0.00406021	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816792	GCTGCAGCCGGAGCC[A/T]AACAGTGTCACTCCC	89849
rs748484166	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838174	ACGAAGGACACTGTT[A/G]TTTTAAGTCTGTTAG	89849
rs748501059	snp	A/G	1.67888e-05	0.00289726	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826800	ACCGGACAGTGAAGG[A/G]GTGGGACCTCGGCCG	89849
rs748600343	snp	C/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813245	CACTGCTTTCTACGT[C/T]CTCTGACCCATCCCC	89849
rs748621116	snp	A/G			synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828729	CCTGTCTGTCCTCAG[A/G]GCCGATGGCTTCAAG	89849
rs748678642	snp	A/G			missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841514	CTGGGCTGGGGTAGG[A/G]GCTGCTGGGAGGCTG	89849
rs748729101	snp	A/G	1.70371e-05	0.0029186	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817823	GTGAAGTGGCAGGAG[A/G]AGGAGGAGGGGCTCC	89849
rs748732085	snp	A/G	1.64792e-05	0.00287042	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827239	ACGTGGTGTGTGGGG[A/G]CCATATCATCATTAG	89849
rs748752549	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72816655	TCAGCCCTTTTAGCC[A/G]GAGATAAATTGCATG	89849
rs748755228	snp	C/G	1.85197e-05	0.00304295	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841002	TTTACTTGAGTTGTT[C/G]AGCAATAATGCTGAT	89849
rs748755241	snp	C/T	1.64974e-05	0.00287201	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828366	TTCCTCAGGGGGCCC[C/T]ACTGCACCCAGGTCA	89849
rs748772793	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813064	AGTTCTCCTGGAGGA[A/G]GTGATGCATGATTAG	89849
rs748806104	snp	A/G	1.64844e-05	0.00287087	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828457	GCTGTTCCCGAGACA[A/G]CACACTCAAGGTCAT	89849
rs748827195	snp	C/T	1.74692e-05	0.00295539	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829407	GCCACGACCTGCCTG[C/T]CTGGGCTGGAGCTCT	89849
rs748838832	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821790	CCACCTCAGGGAGGC[C/T]CGGGGCCAACTATAC	89849
rs748847303	snp	A/C	3.31494e-05	0.00407107	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825367	CCTCCTGGCCACTGG[A/C]GGGGCTGACCGCCTG	89849
rs748938354	in-del	-/AAG	1.75007e-05	0.00295805	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840976	TAAGGGAGAAAACCA[-/AAG]AAGCTCATTTTACTT	89849
rs748965358	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824084	AGCCACCTCCCTGAC[A/G]CTGTCCCACTGTGTG	89849
rs748966822	snp	C/T	0.000164788	0.00907562	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842792	CTCAGGAAAAGATAA[C/T]TCATCATCTGTCTGG	89849
rs749015524	in-del	-/CC			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814720	ACTGCCAGGACTCCG[-/CC]CCTTGCCATCCAGGC	89849
rs749034330	snp	A/C	1.65861e-05	0.00287972	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825376	CACTGGAGGGGCTGA[A/C]CGCCTGATCCACCTC	89849
rs749096417	snp	C/T	0.000176196	0.0093844	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823752	GGAACCTTCAGCGTC[C/T]CTCCTCCCTGTAGGC	89849
rs749194608	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72831339	TAGTGAAACCTTGTC[C/T]CTACTAAAAATACAA	89849
rs749254141	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72832169	CCCTCATTTCACAGG[C/G]TTGTAGTGGAGACTG	89849
rs749292068	snp	A/G	1.64749e-05	0.00287005	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824025	GTACACACACCAGCC[A/G]GTCCCTTAGCATATC	89849
rs749316023	snp	A/G	1.64741e-05	0.00286998	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824141	AGTGTGTGTGTGCCT[A/G]TGTGTGCACCCACGT	89849
rs749339794	snp	C/T	3.42032e-05	0.00413527	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827139	GTCCTGTGGGGTGGC[C/T]CCCGACAACCCTCCT	89849
rs749372930	snp	A/G	3.30491e-05	0.00406491	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824745	CCAGTTTTAAGAAGA[A/G]GAGAGGTCACTCAAT	89849
rs749469386	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840700	TAGATTAAATGTCCC[A/G]AGATGAGTTGATTTC	89849
rs749470113	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72832684	CTGGAGTGGCCCGCA[C/G]TCATGGGTATAAAAA	89849
rs749518810	snp	A/G	0.000156928	0.00885659	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841560	TGGAGGCAGGGAGGC[A/G]TGTGGCTTGGGGGAA	89849
rs749521440	snp	C/T	2.07303e-05	0.00321943	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841494	GTACAGGGAGCTCCT[C/T]TTATCTGGGCTGGGG	89849
rs749543752	in-del	-/GGG	1.6588e-05	0.00287988	cds-indel, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824762	AGAGGTCACTCAATT[-/GGG]GGAGCCCCTGAGCAG	89849
rs749581122	snp	A/T	6.71344e-05	0.00579333	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822032	CCGCTATCCGCTCTT[A/T]CCGTCCTCCAGGCTG	89849
rs749589263	snp	A/G			splice-donor-variant	ATG16L2	GRCh38.p7	11:72828985	ACAGGGACCCCATTG[A/G]TGAGCATGGCCTCCA	89849
rs749593246	snp	A/G	1.90391e-05	0.00308532	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843115	CAGTTTAGGTCAAAC[A/G]TGACCAAATAAAGAG	89849
rs749598015	snp	C/T	7.37327e-05	0.00607132	intron-variant	ATG16L2	GRCh38.p7	11:72829257	GAGCCAGGTTGCAGG[C/T]GCAGTTCCTGAAGCC	89849
rs749635645	snp	C/G	6.6335e-05	0.00575874	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822409	CCCCCTGGAGGAAGG[C/G]ACCGGGTCTAGCCCC	89849
rs749696419	snp	A/C	0.000149198	0.00863578	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814465	CGGGGCCGGGCGTCC[A/C]CGGTGCCCCCGCAGC	89849
rs749749231	snp	A/G	4.34037e-05	0.00465832	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814600	GAGGATGGCGGCTGA[A/G]GGGACGCGGCTACGG	89849
rs749797227	snp	A/G	0.000149946	0.0086574	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826788	CTGGGAGCCGCGACC[A/G]GACAGTGAAGGAGTG	89849
rs749855075	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835049	ATCTAGGTGGTGTAC[C/T]GAGAACCTGTGGGTT	89849
rs749926518	snp	C/T	1.72012e-05	0.00293263	intron-variant	ATG16L2	GRCh38.p7	11:72829297	CCTGCCCCTCCCTTT[C/T]CCCAGCGCTGCCGTC	89849
rs749927245	snp	A/G	0.000115474	0.00759762	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826620	GGAGGCTGCCTGGAG[A/G]TCAGAGGTCATACCT	89849
rs749977076	snp	A/C	0.00608232	0.0548103	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824018	GCCATTTGTACACAC[A/C]CCAGCCAGTCCCTTA	89849
rs749980446	snp	A/T	1.64901e-05	0.00287137	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826699	ACCTGGGGCCGGGGT[A/T]CAGGAGACACTGTCT	89849
rs749982182	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824081	CTCAGCCACCTCCCT[A/G]ACGCTGTCCCACTGT	89849
rs749984022	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72831908	CAACGTGTTCAGACT[C/T]GCAGTTAGGCAGGGC	89849
rs750028212	snp	A/C			utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817817	CTGAGGGTGAAGTGG[A/C]AGGAGGAGGAGGAGG	89849
rs750052250	snp	C/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840311	AGTGGTAAAGGAATG[C/G]TATCAAAAGCTAATA	89849
rs750081391	snp	A/C	7.24953e-05	0.00602017	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840995	AGCTCATTTTACTTG[A/C]GTTGTTGAGCAATAA	89849
rs750184184	snp	A/G	5.07344e-05	0.00503633	intron-variant	ATG16L2	GRCh38.p7	11:72825262	CTCACAGAGACATGC[A/G]CGGGGAGGGCCGGGG	89849
rs750189689	snp	A/C/G	4.17598e-05	0.00456926	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841632	CCCCTCCAGGAAGGA[A/C/G]AGCCTGGCTGCTTCT	89849
rs750227960	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835285	TTCACACACATTCTT[C/T]CCCTTGGGCCTTATG	89849
rs750253711	snp	G/T	0.000248416	0.0111421	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822226	AGGCGCGCGACCTGC[G/T]GGAGAGGCTCGTGCA	89849
rs750254119	snp	A/C	1.64741e-05	0.00286998	intron-variant	ATG16L2	GRCh38.p7	11:72828879	TCTGCTGTGGCCACT[A/C]CAGCCCGGACAGAAG	89849
rs750285549	in-del	-/ATCC	6.64341e-05	0.00576304	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822021	AGCTTGGGACCCGCT[-/ATCC]ATCCGCTCTTTCCGT	89849
rs750448491	snp	A/G	1.64836e-05	0.0028708	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828963	CCGGGAAACTGGAGA[A/G]CAGACTACAGGGACC	89849
rs750502982	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72831722	ACTCCTGTAGCCACC[A/G]TGACTGAGCCCTTAG	89849
rs750504394	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72832561	GTTCAGCAGAGAGGT[G/T]AAAATAGATGTTGAC	89849
rs750510058	snp	A/G	1.73902e-05	0.0029487	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822458	GCGCCAGGGTCTCAG[A/G]ATGCTTTTTACCCAA	89849
rs750512820	snp	C/G/T	5.35416e-05	0.00517382	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829427	GCTGGAGCTCTTGCC[C/G/T]GAAGCCTGAAGCTTC	89849
rs750550696	snp	C/G	1.86939e-05	0.00305722	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822562	AGAGTGGGGATGGGC[C/G]GGTCCGACCCTTGCG	89849
rs750620083	snp	G/T	4.94711e-05	0.00497324	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816759	GAAGGCTGAGCTGCT[G/T]GACAAGTTCTCAAAG	89849
rs750703393	snp	C/T	0.000115383	0.00759462	stop-gained, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828450	CTGCTCAGCTGTTCC[C/T]GAGACAACACACTCA	89849
rs750733173	snp	C/G	0.000214266	0.0103483	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841449	ATGCCCAGGAGAACC[C/G]TTACCGTTTGCTGAA	89849
rs750742456	snp	A/C	5.28234e-05	0.00513896	intron-variant	ATG16L2	GRCh38.p7	11:72817892	AAATGGGGTAGAGAG[A/C]TGTGGTCCAAGGGAG	89849
rs750803354	snp	C/G	1.64906e-05	0.00287142	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828500	CAGCAACATCCGCCA[C/G]GTGTTCAGGTACCAG	89849
rs750822410	snp	G/T	1.65707e-05	0.00287838	synonymous-codon, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825364	CAGCCTCCTGGCCAC[G/T]GGAGGGGCTGACCGC	89849
rs750842866	in-del	-/T			intron-variant	ATG16L2	GRCh38.p7	11:72834586	ACCTCATTCCATTCC[-/T]TTTTTTTTTTTTTGG	89849
rs750844853	in-del	-/CCTGAAGCCCC	3.65263e-05	0.00427339	intron-variant	ATG16L2	GRCh38.p7	11:72829264	GTTGCAGGCGCAGTT[-/CCTGAAGCCCC]CCTGAAGCCTGCCCC	89849
rs750884736	in-del	-/TGTA			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823372	TTGACTGAGCCCGTC[-/TGTA]TGTGTGAATATATAA	89849
rs750913807	snp	A/C			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821979	GTCTCTGCTCCGAGG[A/C]ATATTCCCACTGGGC	89849
rs750924054	snp	C/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821229	CAGCCTCCTGGTGTG[C/G]TGAGGATGGAAGGAG	89849
rs750992653	snp	A/G	1.90026e-05	0.00308236	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842887	AGATAATTAACAGCC[A/G]GTTGCTTTTGCAACC	89849
rs750994935	snp	C/T	1.67433e-05	0.00289333	intron-variant	ATG16L2	GRCh38.p7	11:72825436	CCCTGCCGGCCAACT[C/T]GGTGCTTCTCTCCAG	89849
rs751172587	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72832092	TTGAAGTGAGGGACA[C/T]GCAGGGACACAGGAG	89849
rs751227206	snp	A/G	1.64939e-05	0.0028717	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826603	AGGTGAGGCCTGACT[A/G]GGGAGGCTGCCTGGA	89849
rs751230493	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72817909	GTGGTCCAAGGGAGC[A/C]AGCCAGTGACGGGTA	89849
rs751267405	snp	C/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813744	GCGACCATGTGGAGC[C/T]GTAAACCCTTCTGCC	89849
rs751337441	snp	C/G/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812633	AATATGGCTCCTTAC[C/G/T]TGAGAGAAACGGCAT	89849
rs751388517	snp	C/G	8.28809e-05	0.00643689	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822079	GCGTGGCGCAGCTGC[C/G]AGAGGCGCGGGCGCA	89849
rs751474918	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829614	ACTTTTTCTCCCAAA[C/G]TAGAAAAAAATGATA	89849
rs751487641	in-del	-/G	0.000635768	0.017818	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823811	TGGTGGGTACTAGTA[-/G]GGTAAGGCAGTTCTT	89849
rs751495094	snp	C/G	0.000280036	0.0118296	intron-variant	ATG16L2	GRCh38.p7	11:72828781	GCTGTGTTCAGGTAT[C/G]TCCGTGAGAGCATAT	89849
rs751497717	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835854	CGCAGGTTCAAGCGA[C/T]TCTCCTGCCTCAGCC	89849
rs751552870	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72825221	GGCTGTGTCTGCACA[A/G]GCACCGGTAAGAGGG	89849
rs751572193	in-del	-/C	0.000308119	0.0124082	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822144	ATGCGGTGCAGCGGG[-/C]CAGCCTACGAGGCGC	89849
rs751572265	snp	C/G	1.64741e-05	0.00286998	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842718	CGCCCATTGAATTCC[C/G]CTTCCCAGAAGCCAT	89849
rs751612236	snp	A/G	6.31652e-05	0.00561949	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822386	GGAAGGGAGGGGGGC[A/G]GCAGCCGCCCCCTGG	89849
rs751650269	snp	C/T			missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822895	AGAGAAGGGAGACTC[C/T]GGCTCTGGCCCCTGA	89849
rs751667754	snp	C/T	1.65589e-05	0.00287736	synonymous-codon, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825352	TGGCCCCAACAGCAG[C/T]CTCCTGGCCACTGGA	89849
rs751737936	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72831909	AACGTGTTCAGACTC[A/G]CAGTTAGGCAGGGCT	89849
rs751738143	snp	C/G	1.81204e-05	0.00300996	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822447	TGCGAGGCGCCGCGC[C/G]AGGGTCTCAGGATGC	89849
rs751768510	snp	A/G	1.7172e-05	0.00293013	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842853	CATACTAGGGAGCAA[A/G]AGAAAAACAAATCTG	89849
rs751787070	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72832826	GCTGGCCAGGGCTTC[C/T]GGAGGCCTAGTTCTA	89849
rs751819707	snp	A/G	8.46418e-05	0.0065049	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829314	CCAGCGCTGCCGTCA[A/G]CGCCGTGGCCTGGTG	89849
rs751834736	snp	C/T	1.66087e-05	0.00288168	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840893	GGTCGCAGTTTGCCA[C/T]ATGAGGTCTCAGGAG	89849
rs751853489	snp	C/T	9.89332e-05	0.00703255	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828495	CGTGTCAGCAACATC[C/T]GCCAGGTGTTCAGGT	89849
rs751899045	snp	A/G	1.72475e-05	0.00293657	intron-variant	ATG16L2	GRCh38.p7	11:72817706	CTTGGGTGCCTTTGG[A/G]CACTTGGGTGAACCG	89849
rs751918940	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823944	AAGTCAAGTTCTTAT[C/T]CCAGACTTGAGAGGT	89849
rs751952468	snp	G/T	1.67784e-05	0.00289636	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817796	CAAGTCCCATCACTG[G/T]TCGCACTGAGGGTGA	89849
rs751969318	snp	C/T	1.76968e-05	0.00297457	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840983	GAAAACCAAAGAAGC[C/T]CATTTTACTTGAGTT	89849
rs751991718	snp	A/G	6.78864e-05	0.00582568	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829310	TTCCCCAGCGCTGCC[A/G]TCAACGCCGTGGCCT	89849
rs752010595	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840459	AACTTTGCAATAATA[C/T]ATTCACCCGGAGAAT	89849
rs752180251	snp	C/T	1.64841e-05	0.00287085	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828444	CTGCACCTGCTCAGC[C/T]GTTCCCGAGACAACA	89849
rs752221997	snp	C/G	6.81234e-05	0.00583584	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824796	GATACCAGATCATCC[C/G]TGTGTGTGTGGCTGC	89849
rs752231293	snp	C/T	0.000145911	0.00854015	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72821717	TGGGCACGCTGGAGT[C/T]GGAGCTGCAGCAGAG	89849
rs752286622	snp	C/G	0.000302046	0.0122854	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822066	GCCCTGGAGGCCCGC[C/G]TGGCGCAGCTGCGAG	89849
rs752362895	snp	A/C	3.29484e-05	0.00405871	intron-variant	ATG16L2	GRCh38.p7	11:72828850	CCCTCCCCTCTGACC[A/C]CCCGTTTTCTTGCTC	89849
rs752417065	snp	A/G	1.70101e-05	0.00291629	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826201	CAACCAGACCCTGGA[A/G]GGAGCTGGTGGCAGC	89849
rs752440169	snp	A/G	1.93351e-05	0.00310921	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826839	GTGAGCCCGAGCCCC[A/G]GCCCCACCTCTCCTC	89849
rs752445311	snp	G/T	1.74909e-05	0.00295722	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829409	CACGACCTGCCTGCC[G/T]GGGCTGGAGCTCTTG	89849
rs752470673	snp	A/G	8.86918e-05	0.00665868	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814577	CTGTGAGTGCGCCCC[A/G]GTGCTGAGAGGATGG	89849
rs752543316	snp	G/T	9.88354e-05	0.00702908	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824107	ACTGTGTGGATGTGG[G/T]GAAGGGGCTTCTGGA	89849
rs752628239	snp	A/G	2.10347e-05	0.00324298	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841467	ACCGTTTGCTGAAGG[A/G]GACCGGGGAAAGTAC	89849
rs752636491	snp	C/T	4.96142e-05	0.00498043	intron-variant, missense	ATG16L2	GRCh38.p7	11:72824715	AATGCCCTCCTGACC[C/T]CAACCCACCTTACCC	89849
rs752643443	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838541	GAGGGCTGCCCCCCT[C/T]TTTGCTCCTAGGGTC	89849
rs752673404	snp	A/C	3.31005e-05	0.00406807	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827315	GGCGCAGGCTGGGGG[A/C]GGACTTGGGGAGGGC	89849
rs752696413	snp	C/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827511	TCCAATGCTGGACTC[C/T]GCCTGGACCTTGCAA	89849
rs752733567	in-del	-/GAT	1.64844e-05	0.00287087	cds-indel, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828732	TCTGTCCTCAGGGCC[-/GAT]GATGGCTTCAAGTGT	89849
rs752770334	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72825056	GAGAGAGGAGGCTGG[C/G]AGGCCAGGAGGCCAG	89849
rs752823580	in-del	-/GT	0.00028005	0.0118299	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824126	GGGCTTCTGGAGTAA[-/GT]GTGTGTGTGTGCCTG	89849
rs752896385	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72818556	TCAGGCTCACCATCT[C/G]CCCCAGAATTTGGCC	89849
rs752980963	snp	A/C	5.67827e-05	0.00532805	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822281	GCGCAACCTGCGCAA[A/C]GAGCGCCGGGAGCGG	89849
rs753038429	snp	G/T	1.68153e-05	0.00289955	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826492	CTCCGGCTTAGCACC[G/T]CTCACTTCCTCTCCC	89849
rs753040414	snp	A/C	2.58856e-05	0.00359752	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822580	TCCGACCCTTGCGTT[A/C]TGCCTCCCGCCCCGC	89849
rs753093468	snp	G/T	7.64555e-05	0.00618239	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822944	GGAAGCTTGTGAGAA[G/T]TGGAAGAGGCCCTTC	89849
rs753122202	snp	C/G			missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828909	GCTATGCACTGGCAG[C/G]CTCCTGTGATGGGGC	89849
rs753124464	snp	A/G	0.000279403	0.0118162	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838894	GCAGGAAACAATTAC[A/G]TAGTTTGTCAGTCAG	89849
rs753180635	snp	A/C/G	5.0661e-05	0.00503273	intron-variant	ATG16L2	GRCh38.p7	11:72816872	GGGCTGCCTGTGCTG[A/C/G]GGCCCTGCCCCTGCT	89849
rs753208235	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841968	TTGCTGAATTTCTGA[C/T]TTCCCCAGGTTTTGT	89849
rs753274488	snp	C/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827545	AGATGGAGATGTACC[C/T]TTTTCCATTTAGTTA	89849
rs753298581	snp	A/C/G	3.33074e-05	0.00408078	missense, synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840885	GACTTACAGGTCGCA[A/C/G]TTTGCCATATGAGGT	89849
rs753359718	snp	C/T	8.48752e-05	0.00651386	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841457	GAGAACCCTTACCGT[C/T]TGCTGAAGGAGACCG	89849
rs753405914	snp	G/T	3.45465e-05	0.00415597	intron-variant	ATG16L2	GRCh38.p7	11:72817907	ATGTGGTCCAAGGGA[G/T]CCAGCCAGTGACGGG	89849
rs753425031	snp	A/G			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827104	AGGACACTGGGTTCT[A/G]GGCCTCAGCTTCTCC	89849
rs753432918	snp	C/T	6.60327e-05	0.00574561	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824167	CACGTGTGTGTCGGG[C/T]TCCCCAGCCCAGGCT	89849
rs753494550	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838690	CCTTGTTTTTTGCTC[C/T]GTTCAAGAGTCATCA	89849
rs753591494	snp	A/G	3.41373e-05	0.00413128	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829304	CTCCCTTTCCCCAGC[A/G]CTGCCGTCAACGCCG	89849
rs753716870	snp	C/G	6.0192e-05	0.00548565	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814539	CGTACGCAAAAGGCG[C/G]TTTTCCTGGAGCTGG	89849
rs753720221	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72836009	CGCCTCGGCCTCCCA[A/C]AGTGCTGGGATTACA	89849
rs753811747	snp	A/G	2.78524e-05	0.00373168	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838878	AGCTGCCCGGACCTG[A/G]GCAGGAAACAATTAC	89849
rs753834491	snp	C/T	7.29315e-05	0.00603825	synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822908	TCTGGCTCTGGCCCC[C/T]GAGCCAGAGCCCCTG	89849
rs753862622	snp	C/G/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815994	TATTTATTTATTTAT[C/G/T]TGAGATGGAGTCTTT	89849
rs753896391	snp	A/G	1.64909e-05	0.00287144	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826705	GGCCGGGGTACAGGA[A/G]ACACTGTCTGGACAC	89849
rs754040049	in-del	-/T	3.52858e-05	0.0042002	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829420	TGCCTGGGCTGGAGC[-/T]CTTGCCCGAAGCCTG	89849
rs754075926	in-del	-/CGGA	1.64751e-05	0.00287007	intron-variant	ATG16L2	GRCh38.p7	11:72828819	CCAAGTGTGCCCTGC[-/CGGA]CGGACCCTGTGTGTG	89849
rs754125732	snp	C/T	1.67722e-05	0.00289583	intron-variant	ATG16L2	GRCh38.p7	11:72825445	CCAACTTGGTGCTTC[C/T]CTCCAGACCCTCTCC	89849
rs754138870	in-del	-/GCA			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815127	GGGCCCCGGGCTGCT[-/GCA]GGTGGATGCTGGCTG	89849
rs754143741	snp	A/C/G	6.61096e-05	0.005749	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827308	GGTGACAGGCGCAGG[A/C/G]TGGGGGAGGACTTGG	89849
rs754250782	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72820489	ACAACACAACATAAA[G/T]GAAAGCAAGTGACAA	89849
rs754257904	snp	A/G	3.44976e-05	0.00415303	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826183	CCCAGGTCGCCTGGA[A/G]GCCAACCAGACCCTG	89849
rs754309110	snp	G/T	3.90244e-05	0.00441709	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822568	GGGATGGGCCGGTCC[G/T]ACCCTTGCGTTCTGC	89849
rs754326534	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72818728	AACTTCTGTGCTCTC[C/T]ATTCATTCTCTCAAC	89849
rs754405300	snp	A/G	3.57686e-05	0.00422883	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829431	GAGCTCTTGCCCGAA[A/G]CCTGAAGCTTCCTTC	89849
rs754408375	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72831668	CTAGTCTACTGAGGC[C/T]ATTCCCGTTTCCAGG	89849
rs754477675	snp	A/G	3.31868e-05	0.00407336	intron-variant	ATG16L2	GRCh38.p7	11:72817911	GGTCCAAGGGAGCCA[A/G]CCAGTGACGGGTACT	89849
rs754522632	in-del	-/CAGA			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815453	CACTTCTCCACTGCT[-/CAGA]CAGACAGTGGAACCG	89849
rs754535414	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72835940	TTCGGTAGAGACTGG[C/G]TTTCTCCATGTTGGT	89849
rs754669980	snp	A/T	4.69517e-05	0.00484496	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72821702	AGAAGGGCGCGGCCC[A/T]GGGCACGCTGGAGTC	89849
rs754678386	snp	A/C	1.67885e-05	0.00289724	intron-variant	ATG16L2	GRCh38.p7	11:72825448	ACTTGGTGCTTCTCT[A/C]CAGACCCTCTCCTCA	89849
rs754714669	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72834813	TGGTCTCAAACTCCT[G/T]ATCTCAGGTGATCCA	89849
rs754790128	snp	C/G	1.651e-05	0.0028731	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826641	GGTCATACCTCAGGA[C/G]TAGGGGGCCTGTTAT	89849
rs754914153	snp	A/G	1.84862e-05	0.00304019	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841003	TTACTTGAGTTGTTG[A/G]GCAATAATGCTGATG	89849
rs754934749	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72832203	AGAGAGCCCAGAGGA[A/G]GTGCTCAGGAAATGG	89849
rs754974392	in-del	-/TG	1.6473e-05	0.00286988	frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824094	CTGACGCTGTCCCAC[-/TG]TGTGGATGTGGTGAA	89849
rs754991850	snp	C/T	3.29462e-05	0.00405857	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824090	CTCCCTGACGCTGTC[C/T]CACTGTGTGGATGTG	89849
rs755032564	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829627	AAGTAGAAAAAAATG[A/G]TATCTGAACTGCGTC	89849
rs755033439	snp	A/T	5.01056e-05	0.00500503	intron-variant	ATG16L2	GRCh38.p7	11:72816856	GGTCCGTGGTCACAA[A/T]GGGCTGCCTGTGCTG	89849
rs755066191	in-del	-/GCCGAGCGCAACCTGCGC	0.000254939	0.0112874	cds-indel, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822260	AAGGCGCGCGCCGCG[-/GCCGAGCGCAACCTGCGC]GCCGAGCGCAACCTG	89849
rs755174406	snp	C/G	2.25864e-05	0.00336046	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841562	GAGGCAGGGAGGCGT[C/G]TGGCTTGGGGGAAGG	89849
rs755184931	snp	A/G	1.78819e-05	0.00299009	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824832	TTCCTACCCGGGCTC[A/G]GGATGTGCTGGTAAG	89849
rs755193106	snp	A/G			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820876	GTGAGGCGGGAGTGC[A/G]GATGAAATGACCCTC	89849
rs755237867	snp	G/T	1.76855e-05	0.00297362	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822088	AGCTGCGAGAGGCGC[G/T]GGCGCAGCAGGCCCA	89849
rs755243243	in-del	-/TTTC			intron-variant	ATG16L2	GRCh38.p7	11:72819744	GAGGAGGCTTTTTCT[-/TTTC]TTTCTTTTTTTTTTT	89849
rs755246286	snp	C/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823055	TGGAGCCAGCTCTTG[C/G]GTTGGGAGGGGGCTT	89849
rs755289006	snp	C/T	8.62061e-05	0.00656473	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826810	GAAGGAGTGGGACCT[C/T]GGCCGTGCCTATTGT	89849
rs755296773	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815150	GCTGGCTGAGCCCAG[C/T]GAAGTCGGACTCTCA	89849
rs755347275	snp	A/G	0.000363672	0.0134798	intron-variant	ATG16L2	GRCh38.p7	11:72828700	CTAGTGATGACCTCT[A/G]TTCTGACCCCAGCCC	89849
rs755408336	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841100	TTGAGGCCAGAAGTT[C/T]AAGGCTGCAGTGAGC	89849
rs755416638	snp	C/G/T	5.40666e-05	0.00519912	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829432	AGCTCTTGCCCGAAG[C/G/T]CTGAAGCTTCCTTCG	89849
rs755467465	snp	C/T	1.71053e-05	0.00292444	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827140	TCCTGTGGGGTGGCT[C/T]CCGACAACCCTCCTC	89849
rs755474307	snp	C/T	1.64879e-05	0.00287118	utr-variant-5-prime, stop-gained, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816781	TTCTCAAAGAAGCTG[C/T]AGCCGGAGCCAAACA	89849
rs755534483	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840468	ATAATATATTCACCC[A/G]GAGAATAAACGCTCT	89849
rs755539344	snp	C/T	6.00673e-05	0.00547997	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838891	TGAGCAGGAAACAAT[C/T]ACGTAGTTTGTCAGT	89849
rs755540672	snp	A/G	4.34716e-05	0.00466197	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814602	GGATGGCGGCTGAGG[A/G]GACGCGGCTACGGGC	89849
rs755600778	in-del	-/C			intron-variant	ATG16L2	GRCh38.p7	11:72830933	CGTGCCTGGCTATTT[-/C]CCTTGCTATCATGAG	89849
rs755675282	snp	C/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826872	CACCAGCCAGGAGCC[C/T]CAGGCCAGGGCACAA	89849
rs755734270	snp	C/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823975	TACAAGCCTCCAGGT[C/G]TCTGGCAAAGTGTGG	89849
rs755820801	snp	A/G	1.64841e-05	0.00287085	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828451	TGCTCAGCTGTTCCC[A/G]AGACAACACACTCAA	89849
rs755822391	snp	C/T	0.00105585	0.0229524	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821645	GGGCCTCAGCGCCGC[C/T]GTGCCCACCTGTCCG	89849
rs755848282	snp	A/T	0.000691232	0.0185779	intron-variant	ATG16L2	GRCh38.p7	11:72817893	AATGGGGTAGAGAGA[A/T]GTGGTCCAAGGGAGC	89849
rs755859265	snp	C/G	4.9093e-05	0.0049542	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822237	CTGCTGGAGAGGCTC[C/G]TGCAGCGCAAGGCGC	89849
rs755922827	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72832064	GGTCCTGAGCCTGGA[C/T]GGTTAGTATCCCTTG	89849
rs755994711	snp	A/G	3.29468e-05	0.00405861	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842704	GGAAAACTCCAATAC[A/G]CCCATTGAATTCCCC	89849
rs756087040	snp	A/C	1.64931e-05	0.00287163	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828977	AGCAGACTACAGGGA[A/C]CCCATTGGTGAGCAT	89849
rs756138186	snp	C/T	1.65002e-05	0.00287225	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826628	CCTGGAGGTCAGAGG[C/T]CATACCTCAGGACTA	89849
rs756146519	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72835538	TTCCAGATGAGGACA[A/C]AGGCTCAGTCCCCAT	89849
rs756173502	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72818570	TCCCCCAGAATTTGG[C/T]CCACACCGTTTTGAG	89849
rs756217715	snp	C/T	4.36977e-05	0.00467407	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814581	GAGTGCGCCCCGGTG[C/T]TGAGAGGATGGCGGC	89849
rs756225861	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840539	CCTCAAAGAGGCAAA[C/T]AGAGGCCTGGAAAAT	89849
rs756241191	in-del	-/TG	1.64746e-05	0.00287002	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824140	AAGTGTGTGTGTGCC[-/TG]TGTGTGCACCCACGT	89849
rs756268984	snp	A/T	1.6489e-05	0.00287128	utr-variant-5-prime, stop-gained, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816763	GCTGAGCTGCTGGAC[A/T]AGTTCTCAAAGAAGC	89849
rs756276829	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842015	GGTCACAATCACCAC[A/G]CAAACAAGATCGGCA	89849
rs756293852	snp	A/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823957	ATCCCAGACTTGAGA[A/G]GTTACAAGCCTCCAG	89849
rs756350126	snp	A/C	1.64863e-05	0.00287104	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827212	CCATCAATGTCCTTT[A/C]CTACTGTAATGACGT	89849
rs756350179	snp	A/G	1.65184e-05	0.00287384	missense, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824738	CCTTACCCCAGTTTT[A/G]AGAAGAGGAGAGGTC	89849
rs756376046	snp	C/T	1.64955e-05	0.00287184	splice-donor-variant	ATG16L2	GRCh38.p7	11:72828510	CGCCAGGTGTTCAGG[C/T]ACCAGCCTCATGCCT	89849
rs756397849	in-del	-/G	7.82167e-05	0.00625318	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822378	GGTGTCTGGAAGGGA[-/G]GGGGGGCAGCAGCCG	89849
rs756572086	snp	A/G	1.67489e-05	0.00289381	intron-variant	ATG16L2	GRCh38.p7	11:72825437	CCTGCCGGCCAACTT[A/G]GTGCTTCTCTCCAGA	89849
rs756645906	snp	C/G/T	3.2986e-05	0.00406105	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843190	CTGAAACGAGTTCTG[C/G/T]TTCCGTGGAATTGCT	89849
rs756677540	snp	A/G	4.04572e-05	0.00449744	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822400	CAGCAGCCGCCCCCT[A/G]GAGGAAGGGACCGGG	89849
rs756687970	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829499	CCTTGGGATTTAATG[C/G]GGAAGAAGGCCTGGC	89849
rs756832207	snp	A/G			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814903	GTCCCCGGGGTAGGG[A/G]CTTGATCAGTGCACT	89849
rs756855763	snp	G/T	3.82892e-05	0.00437529	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822990	TGACAGTCTCAGAGC[G/T]CTGAGCTGAGCCCCA	89849
rs756899598	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838710	AAGAGTCATCATCAT[A/G]CAAAGGTGCCTAAAA	89849
rs756931464	snp	C/T			synonymous-codon, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827243	GGTGTGTGGGGACCA[C/T]ATCATCATTAGTGGC	89849
rs756944346	snp	A/T	1.7213e-05	0.00293364	intron-variant	ATG16L2	GRCh38.p7	11:72817708	TGGGTGCCTTTGGGC[A/T]CTTGGGTGAACCGGG	89849
rs756945666	snp	C/T	1.7149e-05	0.00292817	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822010	AGTGACGGGGGAAGC[C/T]TGGGACCCGCTATCC	89849
rs756981735	snp	C/T	1.64765e-05	0.00287019	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824015	ACAGCCATTTGTACA[C/T]ACACCAGCCAGTCCC	89849
rs757068887	snp	A/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823198	CTCCTTCTTGGGATC[A/G]GAGCTCTGGGGGTGG	89849
rs757182952	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72833256	CTGACACCATCAGAC[A/G]TGGACCCATCTGTGA	89849
rs757189973	snp	A/C/T	8.92168e-05	0.00667844	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841559	GTGGAGGCAGGGAGG[A/C/T]GTGTGGCTTGGGGGA	89849
rs757217013	snp	A/G	8.46059e-05	0.00650352	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822081	GTGGCGCAGCTGCGA[A/G]AGGCGCGGGCGCAGC	89849
rs757235088	snp	A/C	7.00525e-05	0.00591788	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841617	AGGTTACCCGGTGCT[A/C]CCCTCCAGGAAGGAG	89849
rs757251971	snp	A/G	1.75835e-05	0.00296504	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826251	ACCCCTCGGTGAGGA[A/G]CTCTGCCCCAGTGGC	89849
rs757288498	snp	A/G	1.64749e-05	0.00287005	intron-variant	ATG16L2	GRCh38.p7	11:72828867	CCGTTTTCTTGCTCT[A/G]CTGTGGCCACTACAG	89849
rs757322028	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823895	CGACCTTCCTGGGAC[C/T]GATCTGGGTCACCCT	89849
rs757395430	snp	C/T	3.31378e-05	0.00407036	intron-variant	ATG16L2	GRCh38.p7	11:72828999	GGTGAGCATGGCCTC[C/T]ACCTGGCCACCTGCC	89849
rs757397648	snp	C/T	1.86743e-05	0.00305562	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842885	TAAGATAATTAACAG[C/T]CGGTTGCTTTTGCAA	89849
rs757453631	snp	A/G	1.65616e-05	0.00287759	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826771	GAGGCACCAGGCAGT[A/G]ACTGGGAGCCGCGAC	89849
rs757484520	in-del	-/CT	1.64746e-05	0.00287002	intron-variant	ATG16L2	GRCh38.p7	11:72828842	TGTGTGTGCCCTCCC[-/CT]CTGACCCCCCGTTTT	89849
rs757491196	snp	A/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842259	CAGTGAGGGAGAGAG[A/C]GAGCCAGCTAAGAGT	89849
rs757495319	snp	C/G	0.000553557	0.0166274	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814426	GGGAGGAACGCGCCG[C/G]TAGGCGGGAGAGCGC	89849
rs757495469	snp	C/T			missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838837	TTCTCTGCTGGCCTT[C/T]GGTGATTCTGTGTAG	89849
rs757537164	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72832750	CAGAGCAGAGCTGGG[A/C]TAAGAACCCAGACCT	89849
rs757540902	snp	A/G			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829691	ACCTTTGGGCTAGTG[A/G]GCTCTGGAAGATCCA	89849
rs757549734	snp	A/G/T	5.33854e-05	0.00516627	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822450	GAGGCGCCGCGCCAG[A/G/T]GTCTCAGGATGCTTT	89849
rs757571634	snp	C/T	1.67829e-05	0.00289675	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817798	AGTCCCATCACTGGT[C/T]GCACTGAGGGTGAAG	89849
rs757623880	snp	A/C	1.77112e-05	0.00297578	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840984	AAAACCAAAGAAGCT[A/C]ATTTTACTTGAGTTG	89849
rs757633057	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837686	TACTTGTGCAGGGTG[C/T]GCAATCCTTCAGTCC	89849
rs757651167	in-del	-/A	1.98908e-05	0.00315357	intron-variant	ATG16L2	GRCh38.p7	11:72824884	TGGGGCAGTGGTGAG[-/A]GAGTGCAGGCACAGG	89849
rs757754438	snp	C/T	1.68932e-05	0.00290625	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827344	GCTGGGGACAGGGCT[C/T]CCAAGTTCTTGTTCC	89849
rs757795559	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829485	GGGACTGGAGCTGGC[C/T]TTGGGATTTAATGGG	89849
rs757809558	snp	C/T	1.67262e-05	0.00289185	intron-variant	ATG16L2	GRCh38.p7	11:72825281	GGAGGGCCGGGGCAC[C/T]AACCTCCCCTTTCCC	89849
rs757862655	snp	A/T	3.3123e-05	0.00406945	missense, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825354	GCCCCAACAGCAGCC[A/T]CCTGGCCACTGGAGG	89849
rs757895538	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72820495	CAACATAAATGAAAG[A/C]AAGTGACAAGTGAGA	89849
rs758019259	snp	C/T	1.69934e-05	0.00291486	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826206	AGACCCTGGAGGGAG[C/T]TGGTGGCAGCATCAC	89849
rs758062360	snp	A/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72816241	CGCCTCGGCCTCCCA[A/G]AGCGCTGGGAATTCA	89849
rs758070793	snp	A/G	2.63459e-05	0.00362936	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822582	CGACCCTTGCGTTCT[A/G]CCTCCCGCCCCGCCT	89849
rs758071790	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824114	GGATGTGGTGAAGGG[A/G]CTTCTGGAGTAAGTG	89849
rs758222991	in-del	-/CAGCAGGCC	0.000102454	0.00715656	cds-indel, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822092	CGAGAGGCGCGGGCG[-/CAGCAGGCC]CAGCAGGCCCAGCAG	89849
rs758309188	snp	C/T	2.10104e-05	0.0032411	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841470	GTTTGCTGAAGGAGA[C/T]CGGGGAAAGTACAGG	89849
rs758316776	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824046	TTAGCATATCTCTCT[C/T]GGTTTTGTCTCAGGT	89849
rs758321662	snp	A/G			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827532	GACCTTGCAACCAAG[A/G]TGGAGATGTACCTTT	89849
rs758352282	snp	A/C	1.65288e-05	0.00287474	intron-variant, synonymous-codon	ATG16L2	GRCh38.p7	11:72824720	CCTCCTGACCCCAAC[A/C]CACCTTACCCCAGTT	89849
rs758364386	snp	C/G	1.65652e-05	0.0028779	intron-variant	ATG16L2	GRCh38.p7	11:72828547	CCTGTGGCCTTTGCT[C/G]GGACAGCTGAGCCTC	89849
rs758404774	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72834292	AGAGGGCTGGGCAGT[C/G]ATTGGCCACAAAACC	89849
rs758449802	snp	A/G	9.66791e-05	0.00695199	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72821729	AGTCGGAGCTGCAGC[A/G]GAGGCAAAGCAGGTG	89849
rs758458018	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835659	TTATAGGAAGCCAAT[C/T]TGGCAAAATCTAACA	89849
rs758540990	snp	C/G	1.65192e-05	0.00287391	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842603	TCTTTTAATTCAACT[C/G]TCTCCCCTCTCAGGT	89849
rs758554756	snp	C/T	1.65081e-05	0.00287293	splice-donor-variant	ATG16L2	GRCh38.p7	11:72828986	CAGGGACCCCATTGG[C/T]GAGCATGGCCTCCAC	89849
rs758594623	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72831897	TCTTTTTAAAGCAAC[A/G]TGTTCAGACTCGCAG	89849
rs758595614	snp	A/C	1.64735e-05	0.00286993	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842713	CAATACGCCCATTGA[A/C]TTCCCCTTCCCAGAA	89849
rs758631087	snp	A/G	2.50737e-05	0.00354065	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822289	TGCGCAACGAGCGCC[A/G]GGAGCGGTGAGGGAG	89849
rs758641384	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72831158	GAATAGATTATTTCC[C/T]GGGATCAGGCCTGGC	89849
rs758731122	snp	A/G	4.94588e-05	0.00497262	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816796	CAGCCGGAGCCAAAC[A/G]GTGTCACTCCCACCA	89849
rs758739273	in-del	-/AG			intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821401	CGGGTTGCTCTTGCC[-/AG]AGAGGTTCCTAGTAG	89849
rs758866538	in-del	-/TG			intron-variant	ATG16L2	GRCh38.p7	11:72818664	TGTAGAGGAGGAAAC[-/TG]AGGCTTGGAGAGGTA	89849
rs758900995	snp	C/T	3.27509e-05	0.00404653	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838899	AAACAATTACGTAGT[C/T]TGTCAGTCAGTTCCT	89849
rs758939971	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72820274	GTGTATATGTCCTTT[A/G]TCATTTTATCACGTG	89849
rs758954622	snp	A/G	1.64789e-05	0.0028704	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827244	GTGTGTGGGGACCAT[A/G]TCATCATTAGTGGCC	89849
rs759007993	snp	A/C	1.66032e-05	0.0028812	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827326	GGGGAGGACTTGGGG[A/C]GGGCTGGGGACAGGG	89849
rs759019193	snp	A/G	1.67114e-05	0.00289057	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827168	CTCTGAGGCCCTGGG[A/G]TCTGCTGCTTGGTCC	89849
rs759172900	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72831422	GAGGCAGGAGAATCA[C/T]GGAACCCAGGAGGAG	89849
rs759205526	snp	C/T	2.08392e-05	0.00322787	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841534	CTGGGAGGCTGGTCG[C/T]ACAACGGCAGTGGAG	89849
rs759212308	snp	C/T	2.04301e-05	0.00319603	intron-variant	ATG16L2	GRCh38.p7	11:72826138	TTGTGAGGTTAAGAC[C/T]TCATTTCAACTGTCC	89849
rs759250549	snp	C/T	1.67877e-05	0.00289716	stop-gained, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824780	GGAGCCCCTGAGCAG[C/T]GATACCAGATCATCC	89849
rs759253273	snp	A/G	5.09498e-05	0.00504701	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822512	TCCCAGGAGCTGAAG[A/G]AGGCTGCCAAGCGGA	89849
rs759268382	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838437	CAGTAATATACTGTA[C/T]GAGTGCACATGATCA	89849
rs759309439	snp	G/T	7.357e-05	0.00606462	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822055	CCAGGCTGGCAGCCC[G/T]GGAGGCCCGCGTGGC	89849
rs759322538	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837092	ACTGCTCTATTTAAT[A/G]AGCATTTGAAGATTT	89849
rs759325995	snp	G/T	1.96342e-05	0.00313316	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822438	CCGCCTGCGTGCGAG[G/T]CGCCGCGCCAGGGTC	89849
rs759329092	snp	C/T	5.93102e-05	0.00544533	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814540	GTACGCAAAAGGCGC[C/T]TTTCCTGGAGCTGGT	89849
rs759337407	in-del	-/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842490	CCAAATGCAGTTGTG[-/C]AGACACTGGCAACCA	89849
rs759338509	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72819894	GGGACTACAGGCGCC[C/T]GCCACCATGCCCGGC	89849
rs759357590	in-del	-/TTTCAGTC	0.00010313	0.00718014	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843138	ATAAAGAGTGCCTTG[-/TTTCAGTC]TTTACCACTGGCATC	89849
rs759361205	snp	A/G	6.93457e-05	0.00588796	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829397	TGGCAGTAGGGCCAC[A/G]ACCTGCCTGCCTGGG	89849
rs759418387	snp	C/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826831	TGCCTATTGTGAGCC[C/T]GAGCCCCAGCCCCAC	89849
rs759439878	snp	A/G			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827427	TGTGGGGCTGGCACT[A/G]CCAGCTAGTGCCTCT	89849
rs759441184	in-del	-/AA			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841343	AGACTCTGTCTCCAA[-/AA]AAAAAAAAAAAAAAA	89849
rs759445648	in-del	-/T	1.64844e-05	0.00287087	frameshift-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828481	GGTCATCGACCTGCG[-/T]TGTCAGCAACATCCG	89849
rs759527212	snp	C/T	1.65091e-05	0.00287303	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816733	CACTCTCCAGATAAC[C/T]ATCTCTTAGAGAAGG	89849
rs759537329	snp	A/G	3.36462e-05	0.00410146	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817766	GGCAGGGAGGAGTCA[A/G]AGCTTGACTCAGACC	89849
rs759544589	snp	A/G	3.30693e-05	0.00406615	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838803	TCATCACACCAGTGT[A/G]ATTTCCACATCTTCA	89849
rs759630130	snp	A/G	1.6904e-05	0.00290719	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840868	AATCCTGCAAGATCA[A/G]AGACTTACAGGTCGC	89849
rs759643947	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835150	GCAGTTAGCTGAGCT[C/T]TGCCCTTGGTCACAG	89849
rs759645953	snp	C/G	7.17592e-05	0.00598953	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823837	TTCTTCCCATCATGA[C/G]GGAGACCTTGGGAGA	89849
rs759802802	snp	A/G	1.68533e-05	0.00290282	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840951	GTGACTCAGCATGAA[A/G]GCTTTTTTCTAAGGG	89849
rs759807516	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72833889	CATAGTGCCATCACA[C/T]TCCAGCCTGGGTGAC	89849
rs759829275	snp	A/C/G	4.94477e-05	0.0049721	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828423	CTGAGCCTCAGCCAC[A/C/G]ACCAACTGCACCTGC	89849
rs759837975	snp	G/T	1.64743e-05	0.00287	intron-variant	ATG16L2	GRCh38.p7	11:72828845	GTGTGCCCTCCCCTC[G/T]GACCCCCCGTTTTCT	89849
rs759939145	snp	C/T	0.000341472	0.0130621	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822152	GCAGCGGGCAGCCTA[C/T]GAGGCGCTGCGCGCG	89849
rs759979352	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72825014	CCACTCAAGCATGTT[A/G]TGATGTGGGCATAAG	89849
rs760026309	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72830909	AGCTGGGCCTATAGG[C/T]GCATGCCACCGTGCC	89849
rs760032306	snp	A/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828917	CTGGCAGGCTCCTGT[A/G]ATGGGGCCCTTTACA	89849
rs760089327	snp	A/G	1.64874e-05	0.00287113	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826578	TGGAAGGTGGGGGAG[A/G]CACAGTCCAAGGTGA	89849
rs760108741	in-del	-/AAAA			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72827969	AAAACAAAACAAAAC[-/AAAA]AAACAAAGCTAGAGC	89849
rs760134544	snp	C/G	1.70481e-05	0.00291955	utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814514	CGTGCGGCAGCTGCG[C/G]CTTCGGGACCGTACG	89849
rs760141265	snp	C/T	1.67978e-05	0.00289804	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822918	GCCCCTGAGCCAGAG[C/T]CCCTGGAGAAGGAAG	89849
rs760194617	snp	C/T	3.29777e-05	0.00406051	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826700	CCTGGGGCCGGGGTA[C/T]AGGAGACACTGTCTG	89849
rs760194771	snp	A/G	5.06547e-05	0.00503237	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829367	AGCGTGGACCAGGGC[A/G]GGAAGGTTGTGCTCT	89849
rs760196463	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842007	GGCTAAGGGGTCACA[A/G]TCACCACGCAAACAA	89849
rs760288892	in-del	-/T	3.30756e-05	0.00406654	splice-donor-variant	ATG16L2	GRCh38.p7	11:72816828	CACCAGGGCCCCTGG[-/T]TAAGTGTATGTGGGT	89849
rs760297673	snp	C/T	1.65021e-05	0.00287241	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824163	CACCCACGTGTGTGT[C/T]GGGCTCCCCAGCCCA	89849
rs760347351	snp	C/T	2.13751e-05	0.00326911	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841454	CAGGAGAACCCTTAC[C/T]GTTTGCTGAAGGAGA	89849
rs760413646	snp	A/G	0.00134971	0.0259429	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814438	CCGCTAGGCGGGAGA[A/G]CGCGGCCATGGCGGG	89849
rs760470731	snp	C/T			utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821653	GCGCCGCCGTGCCCA[C/T]CTGTCCGCCCCCAGA	89849
rs760497980	snp	C/T	1.66985e-05	0.00288946	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842838	AGTGCTTTCACAAAA[C/T]ATACTAGGGAGCAAG	89849
rs760510329	snp	A/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839231	GGTAGAGAGTTACAA[A/C]AGAGAAGGCTAGAAA	89849
rs760518536	snp	A/G	1.66313e-05	0.00288364	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825398	ATCCACCTCTGGAAT[A/G]TTGTGGGAAGTAAGG	89849
rs760594916	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839859	TAGATGAGGTCATTC[A/G]GCAAGAGTGCGTTCA	89849
rs760598434	snp	A/C			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822378	CGGTGTCTGGAAGGG[A/C]GGGGGGCAGCAGCCG	89849
rs760683004	snp	A/G	5.00063e-05	0.00500006	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843155	TCAGTCTTTACCACT[A/G]GCATCTCCGTTGAGG	89849
rs760685701	in-del	-/G			intron-variant	ATG16L2	GRCh38.p7	11:72829270	GGCGCAGTTCCTGAA[-/G]CCCCCCTGAAGCCTG	89849
rs760710191	snp	C/T	1.71408e-05	0.00292747	intron-variant	ATG16L2	GRCh38.p7	11:72829300	GCCCCTCCCTTTCCC[C/T]AGCGCTGCCGTCAAC	89849
rs760724944	snp	C/T			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828217	GGGAGATGAGTCACT[C/T]GCAGCCTTTACCCCA	89849
rs760744047	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835190	CCAGTACCGAAAGCA[A/G]CTTTCACTGGCAGGG	89849
rs760771712	in-del	-/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837906	TCAACAATGCAGGTA[-/T]TGTGTCCTCAACTTA	89849
rs760772829	snp	C/G	2.51569e-05	0.00354652	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838859	TCTGTGTAGGTGGAG[C/G]GGGAGCTGCCCGGAC	89849
rs760777707	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72825928	TGCTCTACATAGTCC[C/T]TTCTCCCTGGTCCTC	89849
rs760810445	in-del	-/GTATGTCC	3.29495e-05	0.00405877	splice-donor-variant	ATG16L2	GRCh38.p7	11:72828777	CAAAGCTGTGTTCAG[-/GTATGTCC]GTGAGAGCATATGCC	89849
rs760895516	snp	C/T	0.000147667	0.00859137	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821647	GCCTCAGCGCCGCCG[C/T]GCCCACCTGTCCGCC	89849
rs760970365	snp	A/G	2.06145e-05	0.00321043	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841509	CTTATCTGGGCTGGG[A/G]TAGGGGCTGCTGGGA	89849
rs761084631	snp	A/G	3.32723e-05	0.00407861	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824766	GTCACTCAATTGGGG[A/G]AGCCCCTGAGCAGCG	89849
rs761102070	snp	A/G/T	0.000352607	0.0132738	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822047	TCCGTCCTCCAGGCT[A/G/T]GCAGCCCTGGAGGCC	89849
rs761133127	snp	C/G	1.64762e-05	0.00287016	intron-variant	ATG16L2	GRCh38.p7	11:72828826	GTGCCCTGCCGGACC[C/G]TGTGTGTGCCCTCCC	89849
rs761238446	snp	A/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813417	TGCCCAGCGAGTCCC[A/T]CCTTTCGTGTCTCAC	89849
rs761238915	snp	C/T	4.94833e-05	0.00497385	intron-variant	ATG16L2	GRCh38.p7	11:72828720	GACCCCAGCCCTGTC[C/T]GTCCTCAGGGCCGAT	89849
rs761289753	snp	C/T	1.75884e-05	0.00296545	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826175	CTGGTCCTCCCAGGT[C/T]GCCTGGAGGCCAACC	89849
rs761340506	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841194	CAAAAATTAGCTGTG[C/T]GTGGTGGTGCATGCC	89849
rs761342720	snp	C/T			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828258	GCCCTGGGGTTCCTC[C/T]GGACTTGGTTAGCTA	89849
rs761346030	snp	C/T	1.65778e-05	0.002879	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842831	ATCATAAAGTGCTTT[C/T]ACAAAACATACTAGG	89849
rs761349330	snp	G/T	9.64553e-05	0.00694394	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822368	CGGGCCTCGCCGGTG[G/T]CTGGAAGGGAGGGGG	89849
rs761500395	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72829220	GAGGGCCTCAAACTA[C/G]CCAGGTCCAGCAGTC	89849
rs761505701	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823463	TGCCTGTCCGCAGGG[C/T]CTCCTCCATCCTTCT	89849
rs761524675	snp	A/C	1.65181e-05	0.00287381	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827304	AGCAGGTGACAGGCG[A/C]AGGCTGGGGGAGGAC	89849
rs761540055	in-del	-/G	1.9528e-05	0.00312468	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822818	CTGGCTTGGTCCCTT[-/G]GCCTTTCTGAACTTC	89849
rs761548534	snp	C/G	3.64817e-05	0.00427078	intron-variant	ATG16L2	GRCh38.p7	11:72829270	GGCGCAGTTCCTGAA[C/G]CCCCCCTGAAGCCTG	89849
rs761628131	in-del	-/G	0.000837872	0.0204508	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821573	GGAAGGGGGCGGGCA[-/G]GGTGAGCAGCCGACT	89849
rs761639720	in-del	-/G			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814930	CACTTAGTCTCGGTA[-/G]CGCAGTGAAAGAACG	89849
rs761680014	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72829242	CCAGCAGTCGGGGCA[C/G]AGCCAGGTTGCAGGC	89849
rs761707500	snp	A/G	0.000509424	0.0159516	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822215	GCTCCAGGAAGAGGC[A/G]CGCGACCTGCTGGAG	89849
rs761722652	snp	A/G	1.64852e-05	0.00287094	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828397	TCCCTGTGCAGGGCC[A/G]GGTCACCTCCCTGAG	89849
rs761774058	snp	A/G	1.66076e-05	0.00288158	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825305	CTTTCCCCACAGGAT[A/G]CCCACCTCTCTGAGG	89849
rs761869339	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842687	TTCCACTAGCACCGA[C/T]GGGAAAACTCCAATA	89849
rs761876318	snp	C/G/T	0.000102868	0.00717113	intron-variant	ATG16L2	GRCh38.p7	11:72817723	ACTTGGGTGAACCGG[C/G/T]GGACATTGAGCACCA	89849
rs761916567	snp	C/T	3.34431e-05	0.00408906	intron-variant	ATG16L2	GRCh38.p7	11:72825427	GGAGCCCTCCCCTGC[C/T]GGCCAACTTGGTGCT	89849
rs761932041	in-del	-/AAAA			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841341	AGAGACTCTGTCTCC[-/AAAA]AAAAAAAAAAAAAAA	89849
rs762002880	snp	C/T	6.60131e-05	0.00574476	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843181	TGAGGCTGCCTGAAA[C/T]GAGTTCTGCTTCCGT	89849
rs762042459	snp	A/G	1.6473e-05	0.00286988	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824070	CTCAGGTCTGCCTCA[A/G]CCACCTCCCTGACGC	89849
rs762056021	snp	G/T	1.76362e-05	0.00296948	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829420	TGCCTGGGCTGGAGC[G/T]CTTGCCCGAAGCCTG	89849
rs762065689	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838244	TCAGGGCAGTCCAAT[C/T]TTTCCCAATAAGGTT	89849
rs762160006	snp	A/G	8.24002e-05	0.0064182	synonymous-codon, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827231	CTGTAATGACGTGGT[A/G]TGTGGGGACCATATC	89849
rs762203122	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72833585	TAGAAGGGCTGTGAG[C/T]CCTGTCCCTGGGTTC	89849
rs762235242	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821852	CTTTCCCTACGTCCC[C/T]CCGACCCCATCGGTT	89849
rs762246965	snp	A/G	2.06383e-05	0.00321228	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841503	GCTCCTCTTATCTGG[A/G]CTGGGGTAGGGGCTG	89849
rs762313226	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72831675	ACTGAGGCCATTCCC[A/G]TTTCCAGGGACACAT	89849
rs762336759	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72830461	CCCCATCCAATCCTT[C/T]CCCTTACTATGGCCA	89849
rs762347999	snp	C/G/T	0.0001715	0.00925876	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841448	CATGCCCAGGAGAAC[C/G/T]CTTACCGTTTGCTGA	89849
rs762367223	snp	A/G	8.43846e-05	0.00649501	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821586	GCAGGTGAGCAGCCG[A/G]CTCCCTTAGCGCCTT	89849
rs762403296	snp	A/G	1.6489e-05	0.00287128	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828496	GTGTCAGCAACATCC[A/G]CCAGGTGTTCAGGTA	89849
rs762416026	snp	G/T			utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817790	TCAGACCAAGTCCCA[G/T]CACTGGTCGCACTGA	89849
rs762421746	snp	C/T	0.000115379	0.00759449	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828476	ACTCAAGGTCATCGA[C/T]CTGCGTGTCAGCAAC	89849
rs762486252	snp	A/C	0.000115307	0.00759211	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842665	CATTTTCTGAGGCTG[A/C]AAGTTCTTCCACTAG	89849
rs762498494	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72833820	CCCAGCTACTTGAGA[G/T]GCTGAGGCAGGAGAA	89849
rs762503254	snp	A/G	0.000156043	0.00883159	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822071	GGAGGCCCGCGTGGC[A/G]CAGCTGCGAGAGGCG	89849
rs762530107	snp	C/T	0.000321285	0.0126704	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822173	GCTGCGCGCGCACGT[C/T]GGGCTCCGGGAGGCG	89849
rs762539163	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828941	CTTTACATCTGGGAT[A/G]TGGACACCGGGAAAC	89849
rs762573347	snp	C/G/T	0.0026817	0.0365223	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822363	GGAGTCGGGCCTCGC[C/G/T]GGTGTCTGGAAGGGA	89849
rs762573350	in-del	-/GG	1.65985e-05	0.00288079	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828311	CTTCCTGTCAGGAGT[-/GG]CCTGGCTAGGCTGTT	89849
rs762585135	snp	C/T	6.64143e-05	0.00576218	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841610	GGAAGCGAGGTTACC[C/T]GGTGCTCCCCTCCAG	89849
rs762638642	snp	C/G	1.64741e-05	0.00286998	intron-variant	ATG16L2	GRCh38.p7	11:72828852	CTCCCCTCTGACCCC[C/G]CGTTTTCTTGCTCTG	89849
rs762669325	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72832031	TCCCTCCCTACATCT[G/T]CACCCTTTTCTATTC	89849
rs762673462	snp	G/T	1.65236e-05	0.00287429	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816826	ACCCACCAGGGCCCC[G/T]GGTAAGTGTATGTGG	89849
rs762680972	snp	C/T	5.08156e-05	0.00504036	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838830	TTCAATCTTCTCTGC[C/T]GGCCTTCGGTGATTC	89849
rs762784721	snp	C/T	6.97946e-05	0.00590698	synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822851	TACCTCTCCTAGGGG[C/T]CCGGACACCCTAGGC	89849
rs762796519	snp	G/T	1.64974e-05	0.00287201	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827200	CAGGCTCCAGGACCA[G/T]CAATGTCCTTTCCTA	89849
rs762812468	in-del	-/TT	0.000155557	0.00881785	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823790	CAGCTTCCCAGGAAC[-/TT]TTGTTGGTGGGTACT	89849
rs762824027	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72818606	ACTCCTTGCAGGCAT[C/T]GGGCTAAACATTGTC	89849
rs762868683	snp	A/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836896	CCTGGATGGAGGGGT[A/T]ATTTTTTAAAAAGGA	89849
rs762903000	snp	A/G	2.07239e-05	0.00321893	intron-variant	ATG16L2	GRCh38.p7	11:72817869	AGGTAAGTTGGGAAG[A/G]GGTCTGAAAATGGGG	89849
rs762926402	snp	C/G	1.64969e-05	0.00287196	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827291	CCGGTTCTGGGACAG[C/G]AGGTGACAGGCGCAG	89849
rs762949035	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72819598	CCCCAGGCTCTTGTC[C/G]CATTTCCTGCCACGC	89849
rs763049308	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72832597	CTCCAGGCTCTCAGC[A/G]GTCACTGCCCAGGTT	89849
rs763068827	snp	A/C	3.29658e-05	0.00405978	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828428	CCTCAGCCACGACCA[A/C]CTGCACCTGCTCAGC	89849
rs763072917	snp	C/T	2.16932e-05	0.00329334	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841439	ATTTAGACCCATGCC[C/T]AGGAGAACCCTTACC	89849
rs763166449	snp	C/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842847	ACAAAACATACTAGG[C/G]AGCAAGAGAAAAACA	89849
rs763269890	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815662	GGGTATAGAGACCTT[C/T]TTTAGGTTTGCTGGG	89849
rs763286955	snp	C/T	1.66971e-05	0.00288934	intron-variant	ATG16L2	GRCh38.p7	11:72825419	GGAAGTAAGGAGCCC[C/T]CCCCTGCCGGCCAAC	89849
rs763337491	in-del	-/GGCTCACTC	1.65842e-05	0.00287955	intron-variant	ATG16L2	GRCh38.p7	11:72816704	TCTGTCTCTGCCCCA[-/GGCTCACTC]TCTTGCACTCTCCAG	89849
rs763349326	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72824929	CAGGGGTGGTCCCAA[A/G]AGGCCAGGGAAGCAA	89849
rs763431629	snp	C/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823560	CTTTCCTTGCAGGTC[C/G]CTGGTGTCCAGGCCT	89849
rs763436009	snp	C/T	4.95005e-05	0.00497471	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826683	CAAACTCTTGATCCG[C/T]ACCTGGGGCCGGGGT	89849
rs763438012	snp	C/G	2.04426e-05	0.00319701	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823786	GGCTCAGCTTCCCAG[C/G]AACTTTTGTTGGTGG	89849
rs763491240	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824060	TTGGTTTTGTCTCAG[A/G]TCTGCCTCAGCCACC	89849
rs763496232	in-del	-/A			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826365	GGCCCCTGGGCTCTT[-/A]ACACAGATCCTCCTC	89849
rs763563880	snp	C/T	1.67789e-05	0.00289641	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817787	GACTCAGACCAAGTC[C/T]CATCACTGGTCGCAC	89849
rs763579653	snp	C/T	2.8598e-05	0.00378129	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822190	GGCTCCGGGAGGCGG[C/T]ACTGCGCAGGCTCCA	89849
rs763589419	snp	A/C/G	5.26887e-05	0.00513245	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840979	GGGAGAAAACCAAAG[A/C/G]AGCTCATTTTACTTG	89849
rs763616318	snp	C/G	4.96701e-05	0.00498323	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826519	TCCCATTTCTCCAGG[C/G]CTACCAGGTTTTAGC	89849
rs763771109	in-del	-/AGG	0.00104027	0.0227828	cds-indel, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817818	TGAGGGTGAAGTGGC[-/AGG]AGGAGGAGGAGGGGC	89849
rs763786268	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835840	CGCAACCTCTGCCTC[A/G]CAGGTTCAAGCGATT	89849
rs763822436	snp	C/G	3.2987e-05	0.00406108	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826601	CAAGGTGAGGCCTGA[C/G]TGGGGAGGCTGCCTG	89849
rs763864788	snp	C/T	1.99047e-05	0.00315467	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826846	CGAGCCCCAGCCCCA[C/T]CTCTCCTCCCCACCA	89849
rs763885595	snp	A/G	1.65381e-05	0.00287555	splice-donor-variant	ATG16L2	GRCh38.p7	11:72816828	CCACCAGGGCCCCTG[A/G]TAAGTGTATGTGGGT	89849
rs763915625	snp	C/T			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828231	TCGCAGCCTTTACCC[C/T]AGCGATCCAGGGCCC	89849
rs763940127	snp	A/G	4.09802e-05	0.00452642	intron-variant	ATG16L2	GRCh38.p7	11:72824891	GTGGTGAGAGAGTGC[A/G]GGCACAGGGGTGGTC	89849
rs764038231	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72826004	CCAGCAGTTAGGGGA[A/G]GTGTAGTCTCCAGCC	89849
rs764042916	snp	A/G			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814896	CCGGGCAGTCCCCGG[A/G]GTAGGGGCTTGATCA	89849
rs764043252	snp	C/T	1.73881e-05	0.00294852	stop-gained, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824813	GTGTGTGTGGCTGCC[C/T]GACTTCCTACCCGGG	89849
rs764106685	snp	C/G	8.2058e-05	0.00640486	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822078	CGCGTGGCGCAGCTG[C/G]GAGAGGCGCGGGCGC	89849
rs764136221	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839238	AGTTACAAAAGAGAA[A/G]GCTAGAAAGGTAGGC	89849
rs764161082	in-del	-/GTGTGCCCTGCCGGACCCTGT	1.64741e-05	0.00286998	intron-variant	ATG16L2	GRCh38.p7	11:72828808	TATGCCTGTGTCCAA[-/GTGTGCCCTGCCGGACCCTGT]GTGTGCCCTGCCGGA	89849
rs764234934	snp	C/T	1.89521e-05	0.00307826	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822442	CTGCGTGCGAGGCGC[C/T]GCGCCAGGGTCTCAG	89849
rs764245364	snp	A/C	3.41664e-05	0.00413304	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842850	AAACATACTAGGGAG[A/C]AAGAGAAAAACAAAT	89849
rs764256374	snp	G/T	3.29669e-05	0.00405984	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828431	CAGCCACGACCAACT[G/T]CACCTGCTCAGCTGT	89849
rs764260536	in-del	-/TAT			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820925	CCAGCGCTGTTCCCA[-/TAT]TGAGTCTGGGCCCTG	89849
rs764311387	snp	C/T	3.29679e-05	0.00405991	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828482	GGTCATCGACCTGCG[C/T]GTCAGCAACATCCGC	89849
rs764311420	snp	A/G	9.93312e-05	0.00704668	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825345	TTCGTTTTGGCCCCA[A/G]CAGCAGCCTCCTGGC	89849
rs764362745	snp	C/T	1.67075e-05	0.00289023	intron-variant	ATG16L2	GRCh38.p7	11:72825423	GTAAGGAGCCCTCCC[C/T]TGCCGGCCAACTTGG	89849
rs764554289	snp	A/G	1.67804e-05	0.00289653	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817792	AGACCAAGTCCCATC[A/G]CTGGTCGCACTGAGG	89849
rs764607462	snp	C/G	2.42269e-05	0.00348035	intron-variant	ATG16L2	GRCh38.p7	11:72817884	GGGTCTGAAAATGGG[C/G]TAGAGAGATGTGGTC	89849
rs764674214	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841272	CCAGGAATTGGTTGC[C/T]ATGAGCCGTGATCAT	89849
rs764805382	snp	C/T	1.64814e-05	0.00287061	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828735	TGTCCTCAGGGCCGA[C/T]GGCTTCAAGTGTGGT	89849
rs764908171	snp	A/G	1.68007e-05	0.00289828	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824781	GAGCCCCTGAGCAGC[A/G]ATACCAGATCATCCC	89849
rs764912788	in-del	-/GGGCGG	0.000498546	0.0157805	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821750	AAGCAGGTGAGGCGC[-/GGGCGG]GGGCGGGGGCGGGAG	89849
rs764951273	snp	A/G	7.40165e-05	0.00608299	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822056	CAGGCTGGCAGCCCT[A/G]GAGGCCCGCGTGGCG	89849
rs764968609	in-del	-/AC	0.000529922	0.016269	frameshift-variant, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822890	AGGGAGAGAAGGGAG[-/AC]ACTCTGGCTCTGGCC	89849
rs765007312	snp	A/G	4.91388e-05	0.00495651	utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814559	CCTGGAGCTGGTGCC[A/G]GCCTGTGAGTGCGCC	89849
rs765010766	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842919	CCCCTATGCTCACAT[A/G]ACAACTAAAAGAGCA	89849
rs765027262	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840005	CGAGGCAAATGTAGA[A/G]AAGCACATCAGCCCA	89849
rs765101251	snp	G/T	1.66241e-05	0.00288302	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827175	GCCCTGGGGTCTGCT[G/T]CTTGGTCCCCAGGCT	89849
rs765181809	snp	A/G	3.78401e-05	0.00434955	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826832	GCCTATTGTGAGCCC[A/G]AGCCCCAGCCCCACC	89849
rs765200178	snp	A/G	1.65075e-05	0.00287289	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816734	ACTCTCCAGATAACC[A/G]TCTCTTAGAGAAGGC	89849
rs765252673	snp	A/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823304	GTGTGCGCAGCCATA[A/G]GTGTGCAAGCATGTG	89849
rs765267559	snp	A/C			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814931	ACTTAGTCTCGGTAG[A/C]GCAGTGAAAGAACGC	89849
rs765280500	snp	C/T	1.65583e-05	0.00287731	intron-variant, synonymous-codon	ATG16L2	GRCh38.p7	11:72824705	GGACTTGCTGAATGC[C/T]CTCCTGACCCCAACC	89849
rs765294104	snp	C/T	0.00060553	0.0173896	intron-variant	ATG16L2	GRCh38.p7	11:72825273	ATGCGCGGGGAGGGC[C/T]GGGGCACCAACCTCC	89849
rs765299930	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72831695	CAGGGACACATGGCT[A/G]GGGAGACCGACACTC	89849
rs765405062	snp	A/G	5.00505e-05	0.00500227	stop-gained, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840882	AGAGACTTACAGGTC[A/G]CAGTTTGCCATATGA	89849
rs765409903	snp	A/G	4.96413e-05	0.00498179	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827314	AGGCGCAGGCTGGGG[A/G]AGGACTTGGGGAGGG	89849
rs765422473	snp	C/G/T	3.35701e-05	0.00409685	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817778	TCAGAGCTTGACTCA[C/G/T]ACCAAGTCCCATCAC	89849
rs765459491	snp	A/G	0.000137781	0.0082989	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840966	GGCTTTTTTCTAAGG[A/G]AGAAAACCAAAGAAG	89849
rs765506311	in-del	-/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842435	GGTGTGGGAGGATGG[-/C]CACATTCCACAAGGG	89849
rs765538493	snp	C/G			synonymous-codon, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827279	TGACCAGAAGATCCG[C/G]TTCTGGGACAGCAGG	89849
rs765573524	snp	C/T	3.29511e-05	0.00405887	intron-variant	ATG16L2	GRCh38.p7	11:72828848	TGCCCTCCCCTCTGA[C/T]CCCCCGTTTTCTTGC	89849
rs765575560	snp	A/C	1.70653e-05	0.00292102	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826193	CTGGAGGCCAACCAG[A/C]CCCTGGAGGGAGCTG	89849
rs765615909	in-del	-/G			intron-variant	ATG16L2	GRCh38.p7	11:72818414	TGTCCCTTCAAATGT[-/G]GGTGTTCTTGGGGTT	89849
rs765815451	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72820548	GCTCAGTGGTGAAAA[G/T]AATTATGTTATAAAT	89849
rs765869209	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72830529	ACACAAAAAACCTTA[A/G]TGCAGCCTCAAACTC	89849
rs765904220	snp	A/G	2.87294e-05	0.00378997	intron-variant	ATG16L2	GRCh38.p7	11:72817897	GGGTAGAGAGATGTG[A/G]TCCAAGGGAGCCAGC	89849
rs765982360	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72832055	TCTATTCTGGGTCCT[A/G]AGCCTGGACGGTTAG	89849
rs766028610	snp	C/G/T	3.62998e-05	0.00426014	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826823	CTCGGCCGTGCCTAT[C/G/T]GTGAGCCCGAGCCCC	89849
rs766064361	snp	A/C	0.000136036	0.00824618	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821661	GTGCCCACCTGTCCG[A/C]CCCCAGATGGCCTAC	89849
rs766081890	snp	A/C/T	6.58941e-05	0.00573964	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842709	ACTCCAATACGCCCA[A/C/T]TGAATTCCCCTTCCC	89849
rs766083733	snp	A/G	3.29973e-05	0.00406172	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824164	ACCCACGTGTGTGTC[A/G]GGCTCCCCAGCCCAG	89849
rs766135378	snp	A/C	1.65004e-05	0.00287227	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828980	AGACTACAGGGACCC[A/C]ATTGGTGAGCATGGC	89849
rs766171873	in-del	-/GGT	1.89066e-05	0.00307457	intron-variant, cds-indel	ATG16L2	GRCh38.p7	11:72823801	GAACTTTTGTTGGTG[-/GGT]ACTAGTAGGGTAAGG	89849
rs766182856	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72833909	GCCTGGGTGACGAGC[A/G]AAACTCCGTCTCAAA	89849
rs766223788	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837083	GTGGCAAGAACTGCT[C/G]TATTTAATAAGCATT	89849
rs766244653	snp	C/T	1.67598e-05	0.00289476	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842840	TGCTTTCACAAAACA[C/T]ACTAGGGAGCAAGAG	89849
rs766370199	snp	C/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822775	GAATTCCTGTCTTCA[C/G]CGTATCCTGTGCTGG	89849
rs766371476	in-del	-/GCGGGCGCAGAATGCGGTGCA	0.00018379	0.00958442	cds-indel, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822119	GCAGGTGGAGGAGTG[-/GCGGGCGCAGAATGCGGTGCA]GCGGGCAGCCTACGA	89849
rs766394206	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72832680	AAATCTGGAGTGGCC[C/T]GCACTCATGGGTATA	89849
rs766430064	snp	A/G	1.64901e-05	0.00287137	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826703	GGGGCCGGGGTACAG[A/G]AGACACTGTCTGGAC	89849
rs766471788	snp	C/T	1.72952e-05	0.00294063	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840856	TATGCATTCGATAAT[C/T]CTGCAAGATCAGAGA	89849
rs766519909	snp	A/G	1.6528e-05	0.00287467	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827305	GCAGGTGACAGGCGC[A/G]GGCTGGGGGAGGACT	89849
rs766526432	snp	C/T	2.61168e-05	0.00361355	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838866	AGGTGGAGGGGGAGC[C/T]GCCCGGACCTGAGCA	89849
rs766544041	snp	G/T	1.64841e-05	0.00287085	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827218	ATGTCCTTTCCTACT[G/T]TAATGACGTGGTGTG	89849
rs766551326	snp	A/G	0.00145388	0.0269226	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822885	GGGATGAGGGAGAGA[A/G]GGGAGACTCTGGCTC	89849
rs766599053	snp	A/G/T	5.32042e-05	0.00515745	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824826	CCCGACTTCCTACCC[A/G/T]GGCTCAGGATGTGCT	89849
rs766635532	snp	A/G	1.64871e-05	0.00287111	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816771	GCTGGACAAGTTCTC[A/G]AAGAAGCTGCAGCCG	89849
rs766647897	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815878	AGGGTGTTCCAGGGT[C/T]AAACCACCAACCTCC	89849
rs766674214	snp	A/G	1.66015e-05	0.00288105	intron-variant	ATG16L2	GRCh38.p7	11:72816841	TGGTAAGTGTATGTG[A/G]GTCCGTGGTCACAAA	89849
rs766704443	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840403	GGAGTACAGTGGTGG[A/G]TGGAATGCAGATGGC	89849
rs766713425	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72828515	GGTGTTCAGGTACCA[A/G]CCTCATGCCTGCTGA	89849
rs766715895	snp	C/T	2.07024e-05	0.00321726	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841510	TTATCTGGGCTGGGG[C/T]AGGGGCTGCTGGGAG	89849
rs766720051	snp	A/G			missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841469	CGTTTGCTGAAGGAG[A/G]CCGGGGAAAGTACAG	89849
rs766768817	snp	C/T	3.29783e-05	0.00406055	intron-variant	ATG16L2	GRCh38.p7	11:72828724	CCAGCCCTGTCTGTC[C/T]TCAGGGCCGATGGCT	89849
rs766890535	snp	A/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823594	GGCAGTGAAGAAACC[A/G]TGGGGAGGGGCATGA	89849
rs767015177	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72820338	TTCACCACTGCAAAG[A/G]TCTCTTTCTTATTAC	89849
rs767027658	snp	A/C	1.64779e-05	0.00287031	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824016	CAGCCATTTGTACAC[A/C]CACCAGCCAGTCCCT	89849
rs767056738	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72818774	CTATATCCAAAGTAC[A/G]GGGAGTGCAACAATA	89849
rs767115370	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837150	TAAAAAAACCACCCT[G/T]TTAATTTCTTTTTTA	89849
rs767118900	snp	A/G	4.94417e-05	0.00497176	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828961	CACCGGGAAACTGGA[A/G]AGCAGACTACAGGGA	89849
rs767133271	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838986	GCACCCTAGGGGTCT[C/T]AGAAATGTTGTGAGC	89849
rs767151376	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835165	TTGCCCTTGGTCACA[A/G]ACGGAACCTCCAGTA	89849
rs767176019	snp	A/C	1.79793e-05	0.00299822	intron-variant	ATG16L2	GRCh38.p7	11:72829276	GTTCCTGAAGCCCCC[A/C]TGAAGCCTGCCCCTC	89849
rs767390327	in-del	-/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842575	ACCCTTTGGGAGCAA[-/T]TTTCTTTAAACATCT	89849
rs767416718	snp	A/G/T	6.62947e-05	0.00575705	synonymous-codon, missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825319	TGCCCACCTCTCTGA[A/G/T]GTCAATGCTGTTCGT	89849
rs767437963	snp	C/T	7.05542e-05	0.00593903	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841618	GGTTACCCGGTGCTC[C/T]CCTCCAGGAAGGAGA	89849
rs767447177	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835167	GCCCTTGGTCACAGA[C/T]GGAACCTCCAGTACC	89849
rs767460946	snp	C/T	0.000507099	0.0159152	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822216	CTCCAGGAAGAGGCG[C/T]GCGACCTGCTGGAGA	89849
rs767464019	in-del	-/C	4.95115e-05	0.00497527	intron-variant	ATG16L2	GRCh38.p7	11:72828516	GTGTTCAGGTACCAG[-/C]CTCATGCCTGCTGAC	89849
rs767468123	snp	A/G	9.13617e-05	0.00675815	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822371	GCCTCGCCGGTGTCT[A/G]GAAGGGAGGGGGGCA	89849
rs767535622	snp	A/C			synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826735	CAAGGATAAGGTGAC[A/C]GCTGCCAAATTCAAG	89849
rs767537588	snp	A/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823870	TTCATTACCAAATCC[A/G]TTGCTGCCCCGACCT	89849
rs767551802	in-del	-/AGTA	4.94189e-05	0.00497062	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824122	TGAAGGGGCTTCTGG[-/AGTA]AGTGTGTGTGTGCCT	89849
rs767590600	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72825015	CACTCAAGCATGTTA[C/T]GATGTGGGCATAAGC	89849
rs767657270	snp	C/T	1.64947e-05	0.00287177	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816750	TCTCTTAGAGAAGGC[C/T]GAGCTGCTGGACAAG	89849
rs767662932	snp	A/G	9.9005e-05	0.0070351	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843182	GAGGCTGCCTGAAAC[A/G]AGTTCTGCTTCCGTG	89849
rs767663873	snp	A/G	5.32203e-05	0.00515823	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829424	TGGGCTGGAGCTCTT[A/G]CCCGAAGCCTGAAGC	89849
rs767752825	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72834103	AGGCAAACACAGGAA[C/G]AGTCTAGGAGGAAAC	89849
rs767771115	snp	A/C	5.59937e-05	0.00529091	intron-variant	ATG16L2	GRCh38.p7	11:72826160	CAACTGTCCCTTCCC[A/C]TGGTCCTCCCAGGTC	89849
rs767819746	snp	A/T	1.81661e-05	0.00301376	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822556	CGAGTAAGAGTGGGG[A/T]TGGGCCGGTCCGACC	89849
rs767840059	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72830657	GTGACTTTCTAGGGT[A/G]TCGTGTTCACAAGTC	89849
rs767867079	snp	G/T			missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828905	AGAAGCTATGCACTG[G/T]CAGGCTCCTGTGATG	89849
rs767867956	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829402	GTAGGGCCACGACCT[A/G]CCTGCCTGGGCTGGA	89849
rs767870522	snp	A/G	1.64906e-05	0.00287142	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828499	TCAGCAACATCCGCC[A/G]GGTGTTCAGGTACCA	89849
rs767993795	snp	A/G	0.00403021	0.0447086	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821627	GGGACTGGAGGCCTG[A/G]AGGGGCCTCAGCGCC	89849
rs768149600	snp	A/G	3.34605e-05	0.00409012	intron-variant	ATG16L2	GRCh38.p7	11:72825428	GAGCCCTCCCCTGCC[A/G]GCCAACTTGGTGCTT	89849
rs768160673	snp	A/C	1.65858e-05	0.00287969	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825377	ACTGGAGGGGCTGAC[A/C]GCCTGATCCACCTCT	89849
rs768160884	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72818989	GGTGATTCTCAAACA[A/T]CTGACCCCCACACCA	89849
rs768171858	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841728	TTAGAGGCAACTGAG[C/T]ATTAAATAACCACCT	89849
rs768228056	snp	A/C	3.25537e-05	0.00403433	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822410	CCCCTGGAGGAAGGG[A/C]CCGGGTCTAGCCCCG	89849
rs768243020	in-del	-/GTCTGT			intron-variant, cds-indel	ATG16L2	GRCh38.p7	11:72824185	CCCAGCCCAGGCTTG[-/GTCTGT]GTCTGTGCCTCGACC	89849
rs768300840	snp	A/G			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824289	AATGGCCTCAGCCCC[A/G]GCCCCGGTTCAGCTG	89849
rs768346952	snp	C/G			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72830029	ATCAAAGTCCTTGGT[C/G]CACAGGGCCTCCCTT	89849
rs768378654	snp	A/T	1.64808e-05	0.00287057	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842795	AGGAAAAGATAACTC[A/T]TCATCTGTCTGGCCC	89849
rs768396524	snp	C/G	1.65127e-05	0.00287334	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842605	TTTTAATTCAACTGT[C/G]TCCCCTCTCAGGTAC	89849
rs768462299	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823450	TTCAGACCTTGGGTG[C/T]CTGTCCGCAGGGTCT	89849
rs768476009	snp	C/T	3.52125e-05	0.00419583	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840849	GAAGAACTATGCATT[C/T]GATAATCCTGCAAGA	89849
rs768503407	snp	C/T	0.000701508	0.0187153	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823755	ACCTTCAGCGTCTCT[C/T]CTCCCTGTAGGCCCC	89849
rs768527873	snp	C/T	3.31879e-05	0.00407343	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840923	GTATGCCTTGATGCC[C/T]GTGAGAATCCTGGTG	89849
rs768531673	snp	A/G	1.65007e-05	0.00287229	splice-donor-variant, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827294	GTTCTGGGACAGCAG[A/G]TGACAGGCGCAGGCT	89849
rs768590038	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838629	AGGCACGAAATATTC[-/A]AAACGTGGGAGGAGT	89849
rs768737301	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836784	ACATTTTATACATAA[C/T]AAATACAAACTTTTT	89849
rs768741002	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838158	TGGCACAGATATTAA[G/T]ACGAAGGACACTGTT	89849
rs768741849	snp	A/G	0.00310135	0.0392563	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817824	TGAAGTGGCAGGAGG[A/G]GGAGGAGGGGCTCCG	89849
rs768771238	snp	A/G	2.1558e-05	0.00328307	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841442	TAGACCCATGCCCAG[A/G]AGAACCCTTACCGTT	89849
rs768793777	snp	A/G	3.41839e-05	0.0041341	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827143	TGTGGGGTGGCTCCC[A/G]ACAACCCTCCTCTGA	89849
rs768856550	snp	C/T	0.000134953	0.00821329	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822033	CGCTATCCGCTCTTT[C/T]CGTCCTCCAGGCTGG	89849
rs768866533	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839258	GAAAGGTAGGCTAGG[A/G]TTAAGTTGTGAAGGG	89849
rs768948303	snp	A/C	1.65477e-05	0.00287638	intron-variant	ATG16L2	GRCh38.p7	11:72828684	CTGCAGAGGGCAGAG[A/C]CTAGTGATGACCTCT	89849
rs768966227	snp	C/G	1.65002e-05	0.00287225	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826685	AACTCTTGATCCGTA[C/G]CTGGGGCCGGGGTAC	89849
rs769001348	snp	A/G	1.64743e-05	0.00287	intron-variant	ATG16L2	GRCh38.p7	11:72828811	TGCCTGTGTCCAAGT[A/G]TGCCCTGCCGGACCC	89849
rs769003516	snp	A/G	1.98876e-05	0.00315332	intron-variant	ATG16L2	GRCh38.p7	11:72826147	TAAGACCTCATTTCA[A/G]CTGTCCCTTCCCCTG	89849
rs769035835	snp	C/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827805	GGGTGTGGTGGCAGA[C/T]GCCTGTAATCGCAGC	89849
rs769087083	snp	G/T	0.000133485	0.00816851	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814476	GTCCCCGGTGCCCCC[G/T]CAGCGCGCTGGAAAC	89849
rs769087653	snp	C/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813430	CCTCCTTTCGTGTCT[C/T]ACAGTAGCCTGAGCC	89849
rs769127298	snp	A/G	1.68151e-05	0.00289953	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829341	GGTGCTACTCCGGGA[A/G]CCACATGGTGAGCGT	89849
rs769144650	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72832370	CTTGCTTGGAGGTCC[C/T]CCTCCCAGTAGGAGG	89849
rs769179882	snp	C/T	1.64743e-05	0.00287	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824146	GTGTGTGCCTGTGTG[C/T]GCACCCACGTGTGTG	89849
rs769182539	snp	A/G	1.66866e-05	0.00288842	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826792	GAGCCGCGACCGGAC[A/G]GTGAAGGAGTGGGAC	89849
rs769191117	snp	A/C			intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843007	TAGGGTTCTACTGTG[A/C]AGGACAAACGTGACC	89849
rs769263801	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837835	ACAGCCTGGCTGTCT[C/G]GGCCGGTCTGCTGGC	89849
rs769264670	in-del	-/CAC	1.64912e-05	0.00287147	cds-indel, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826707	CCGGGGTACAGGAGA[-/CAC]TGTCTGGACACAAGG	89849
rs769322853	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72817574	GGGAATCTTAGAGCA[C/G]AGGAGTCATGGACAG	89849
rs769335561	in-del	-/TTCAGCCCCTCCATATTAGCTCGGCTA	2.45047e-05	0.00350025	cds-indel, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838841	TGCTGGCCTTCGGTG[-/TTCAGCCCCTCCATATTAGCTCGGCTA]ATTCTGTGTAGGTGG	89849
rs769362674	snp	C/T	3.33628e-05	0.00408415	intron-variant	ATG16L2	GRCh38.p7	11:72825287	CCGGGGCACCAACCT[C/T]CCCTTTCCCCACAGG	89849
rs769363155	in-del	-/ATTA			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815973	GCTGGGGAAGTTGGG[-/ATTA]TTTATTTATTTATTT	89849
rs769415235	snp	A/G	1.6486e-05	0.00287102	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827278	ATGACCAGAAGATCC[A/G]GTTCTGGGACAGCAG	89849
rs769466395	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72824883	GTGGGGCAGTGGTGA[A/G]AGAGTGCAGGCACAG	89849
rs769592479	snp	C/G	4.70223e-05	0.0048486	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822159	GCAGCCTACGAGGCG[C/G]TGCGCGCGCACGTCG	89849
rs769595660	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72819370	TTAGCACTCCCTGTC[C/G]CTTCTCCATACAGCT	89849
rs769653254	snp	C/T	1.65151e-05	0.00287355	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816822	CACCACCCACCAGGG[C/T]CCCTGGTAAGTGTAT	89849
rs769683570	snp	A/G	1.65403e-05	0.00287574	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838812	CAGTGTGATTTCCAC[A/G]TCTTCAATCTTCTCT	89849
rs769689284	snp	C/T			missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826242	TGGACTTTGACCCCT[C/T]GGTGAGGAACTCTGC	89849
rs769697470	snp	A/C	5.09472e-05	0.00504688	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822513	CCCAGGAGCTGAAGA[A/C]GGCTGCCAAGCGGAC	89849
rs769760709	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72818531	TGCTTTTTGGAGATC[A/G]CATCTAAAATCAGGC	89849
rs769760770	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72831316	GTTCAAGACCAACCT[A/G]AGCAACATAGTGAAA	89849
rs769823638	snp	G/T	3.29473e-05	0.00405864	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824049	GCATATCTCTCTTGG[G/T]TTTGTCTCAGGTCTG	89849
rs769884957	snp	A/G	1.76446e-05	0.00297018	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817839	AGGAGGAGGGGCTCC[A/G]GCTGGTCTGTGGTGA	89849
rs769922001	snp	A/G	3.32452e-05	0.00407695	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826784	GTGACTGGGAGCCGC[A/G]ACCGGACAGTGAAGG	89849
rs769970369	snp	A/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815441	CTCCAGCAGCCACAC[A/T]TCTCCACTGCTCAGA	89849
rs769972686	snp	C/T	6.58935e-05	0.00573955	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824136	GAGTAAGTGTGTGTG[C/T]GCCTGTGTGTGCACC	89849
rs770072481	snp	C/T	1.64833e-05	0.00287078	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828480	AAGGTCATCGACCTG[C/T]GTGTCAGCAACATCC	89849
rs770086812	snp	A/G	0.000291957	0.0120786	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821521	AGCGCGTCCCTGTGC[A/G]AGGTCCCAAACCTGT	89849
rs770156767	snp	A/G	2.07609e-05	0.0032218	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841484	ACCGGGGAAAGTACA[A/G]GGAGCTCCTCTTATC	89849
rs770188001	snp	A/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828918	TGGCAGGCTCCTGTG[A/G]TGGGGCCCTTTACAT	89849
rs770205461	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72834933	AGCTAAGAGGGAAAG[C/G]TCTTCCATCAAGCAG	89849
rs770218098	snp	C/G	1.73875e-05	0.00294847	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822355	TGCAGGGAGGAGTCG[C/G]GCCTCGCCGGTGTCT	89849
rs770238136	snp	A/G	1.64765e-05	0.00287019	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842764	CTTTGTTCAAGATAC[A/G]GATTATTGCTCCCTC	89849
rs770289267	snp	C/T	1.6679e-05	0.00288777	intron-variant	ATG16L2	GRCh38.p7	11:72829020	GCCACCTGCCTGGCC[C/T]CAGTCCTGCCAGGCT	89849
rs770335519	snp	A/G	1.7141e-05	0.0029275	synonymous-codon, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829387	GGTTGTGCTCTGGCA[A/G]TAGGGCCACGACCTG	89849
rs770354176	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72831342	TGAAACCTTGTCTCT[A/G]CTAAAAATACAAAAT	89849
rs770445836	snp	A/C	3.68793e-05	0.00429398	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838908	CGTAGTTTGTCAGTC[A/C]GTTCCTGACTCAGTA	89849
rs770511266	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813072	TGGAGGAGGTGATGC[A/G]TGATTAGGAGCCAGG	89849
rs770515748	snp	A/T	4.87128e-05	0.00493498	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838776	TGTAGCAGTAATGGA[A/T]GGGCAAGCCCATCAT	89849
rs770617200	in-del	-/AG	2.19065e-05	0.0033095	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841428	AGTGAAAATGCATTT[-/AG]ACCCATGCCCAGGAG	89849
rs770661763	snp	C/T	1.69329e-05	0.00290967	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827155	CCCGACAACCCTCCT[C/T]TGAGGCCCTGGGGTC	89849
rs770707766	snp	A/C	1.66015e-05	0.00288105	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843160	CTTTACCACTGGCAT[A/C]TCCGTTGAGGCTGCC	89849
rs770709340	in-del	-/T	3.3134e-05	0.00407012	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828325	GGCCTGGCTAGGCTG[-/T]TTCCTCATCCCTGTC	89849
rs770712690	snp	A/G	1.64825e-05	0.00287071	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827266	TTAGTGGCCACAATG[A/G]CCAGAAGATCCGGTT	89849
rs770828941	snp	G/T	1.66502e-05	0.00288527	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825405	TCTGGAATGTTGTGG[G/T]AAGTAAGGAGCCCTC	89849
rs770892199	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72832191	TGGAGACTGCTTAGA[A/G]AGCCCAGAGGAGGTG	89849
rs770897339	snp	A/C			intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821285	GCGCCCGAGGGCCGG[A/C]TGGGCATTTGGCAGC	89849
rs770985644	snp	A/G	3.29707e-05	0.00406008	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826573	AGCTCTGGAAGGTGG[A/G]GGAGGCACAGTCCAA	89849
rs771040611	snp	C/G/T	0.000170663	0.00923593	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823770	CCTCCCTGTAGGCCC[C/G/T]GGCTCAGCTTCCCAG	89849
rs771047006	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72829099	CCTCCACCTTCCACC[C/T]GACCAGAGCCCTTTG	89849
rs771067715	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72828601	TGGAGCCCTCCCTGG[A/T]GGCCCCTCCAGACCA	89849
rs771158214	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72818124	CACATGGTTTAGCCT[A/G]CTCTGCTCACTACTC	89849
rs771163251	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72824990	GCCTCCCACAGCCTG[C/T]GGTGGGAGCCACTCA	89849
rs771165970	snp	C/T	3.30126e-05	0.00406266	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826663	GCCTGTTATGGGGTC[C/T]TGGCCAAACTCTTGA	89849
rs771249004	snp	A/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836306	ATTACTCCTTAGGGT[A/G]GAGGTTTAGGAAAGG	89849
rs771298486	in-del	-/CAA	1.71737e-05	0.00293028	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822471	AGGATGCTTTTTACC[-/CAA]CAAGGGCCAAGCAGG	89849
rs771307762	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72817075	GCATTTGTCCCATCT[C/T]CTTCCCGTCCCACCC	89849
rs771324357	snp	A/G	2.75281e-05	0.00370989	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841594	GAGATCTGCAGCAAA[A/G]GGAAGCGAGGTTACC	89849
rs771371980	snp	C/G	1.75711e-05	0.00296399	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822351	CCCCTGCAGGGAGGA[C/G]TCGGGCCTCGCCGGT	89849
rs771389755	snp	C/T	3.29495e-05	0.00405877	intron-variant	ATG16L2	GRCh38.p7	11:72828839	CCCTGTGTGTGCCCT[C/T]CCCTCTGACCCCCCG	89849
rs771410039	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835067	GAACCTGTGGGTTGA[C/T]TGCATCATGCATCAA	89849
rs771442871	snp	C/T	3.29462e-05	0.00405857	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828911	TATGCACTGGCAGGC[C/T]CCTGTGATGGGGCCC	89849
rs771444204	snp	A/G	0.000918414	0.0214094	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822143	GAATGCGGTGCAGCG[A/G]GCAGCCTACGAGGCG	89849
rs771456551	snp	G/T			upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814172	GGAGGCTCCGACCTC[G/T]CTCCTGCTTATGACC	89849
rs771481475	snp	A/G	1.85775e-05	0.00304769	intron-variant	ATG16L2	GRCh38.p7	11:72824849	GATGTGCTGGTAAGG[A/G]AGGAGCTGAGCCACA	89849
rs771517454	in-del	-/ACCATCTC	4.95356e-05	0.00497648	utr-variant-5-prime, frameshift-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816731	TGCACTCTCCAGATA[-/ACCATCTC]TTAGAGAAGGCTGAG	89849
rs771630943	snp	C/T	1.68445e-05	0.00290206	intron-variant	ATG16L2	GRCh38.p7	11:72825459	CTCTCCAGACCCTCT[C/T]CTCAGCTCACTCCTT	89849
rs771649936	snp	C/T	3.32591e-05	0.0040778	intron-variant	ATG16L2	GRCh38.p7	11:72816694	CTGCTGGGTATCTGT[C/T]TCTGCCCCAGGCTCA	89849
rs771688111	snp	C/G	1.70321e-05	0.00291818	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822484	CCCAACAAGGGCCAA[C/G]CAGGCGCGGGTGTCC	89849
rs771693765	snp	A/C/T	3.32012e-05	0.00407427	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842833	CATAAAGTGCTTTCA[A/C/T]AAAACATACTAGGGA	89849
rs771800342	snp	A/G/T	3.36838e-05	0.00410378	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829355	AGCCACATGGTGAGC[A/G/T]TGGACCAGGGCAGGA	89849
rs771809767	snp	G/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841773	GCATTGCACTTCACT[G/T]TTTCCTCTTACAGAT	89849
rs771836595	snp	C/G	6.65956e-05	0.00577004	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822214	GGCTCCAGGAAGAGG[C/G]GCGCGACCTGCTGGA	89849
rs771853466	snp	A/G	5.49345e-05	0.00524063	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838758	TCCAAGCCTGGCCTT[A/G]ATTGTAGCAGTAATG	89849
rs771922954	snp	A/G	1.74811e-05	0.00295639	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817833	AGGAGGAGGAGGAGG[A/G]GCTCCGGCTGGTCTG	89849
rs771962828	in-del	-/TG			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823288	CAGTCATGCCAGGCA[-/TG]TGTGCGCAGCCATAG	89849
rs771967114	snp	C/T	1.64849e-05	0.00287092	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828401	TGTGCAGGGCCGGGT[C/T]ACCTCCCTGAGCCTC	89849
rs771975030	snp	G/T	1.87802e-05	0.00306427	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822121	AGGTGGAGGAGTGGC[G/T]GGCGCAGAATGCGGT	89849
rs772314744	snp	A/C	1.64738e-05	0.00286995	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828889	CCACTACAGCCCGGA[A/C]AGAAGCTATGCACTG	89849
rs772383877	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72819196	TCGTTCTCACACATG[C/G]TGGAAATGCAGGGGC	89849
rs772397859	snp	C/G			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826468	ATTCTGTGGCCCGAA[C/G]AATGTTGCCTCCGGC	89849
rs772442655	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838023	TTATATTGGCTAATT[G/T]CAGATCCGGAAGTTC	89849
rs772451287	snp	C/T	1.73456e-05	0.00294491	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822853	CCTCTCCTAGGGGCC[C/T]GGACACCCTAGGCGA	89849
rs772451381	snp	A/G	1.64866e-05	0.00287106	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826559	CAACCAGGCTGCCCA[A/G]CTCTGGAAGGTGGGG	89849
rs772469113	snp	C/G	4.69859e-05	0.00484672	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841570	GAGGCGTGTGGCTTG[C/G]GGGAAGGAGAGATCT	89849
rs772555777	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72825794	AGACAAGTATGAACT[A/G]TTGGCCTTGTCCCAA	89849
rs772574751	snp	A/G	8.35596e-05	0.00646319	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843152	GTTTCAGTCTTTACC[A/G]CTGGCATCTCCGTTG	89849
rs772588181	snp	A/G	4.11879e-05	0.00453787	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841507	CTCTTATCTGGGCTG[A/G]GGTAGGGGCTGCTGG	89849
rs772607000	snp	A/G			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827075	AAGCGGAAGACCTGG[A/G]TTCTAGTCTTGGGAG	89849
rs772633981	snp	G/T	3.43265e-05	0.00414271	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814510	ACATCGTGCGGCAGC[G/T]GCGGCTTCGGGACCG	89849
rs772692861	snp	C/T	2.17162e-05	0.00329509	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822427	CGGGTCTAGCCCCGC[C/T]TGCGTGCGAGGCGCC	89849
rs772746188	snp	A/C	1.70284e-05	0.00291786	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822485	CCAACAAGGGCCAAG[A/C]AGGCGCGGGTGTCCC	89849
rs772752797	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841279	TTGGTTGCTATGAGC[C/T]GTGATCATGCCACTG	89849
rs772754047	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72830336	GGCCATCATCTCCCC[C/T]GCAAGTGACCCGTTC	89849
rs772757361	in-del	-/G	3.47464e-05	0.00416797	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826180	CCTCCCAGGTCGCCT[-/G]GAGGCCAACCAGACC	89849
rs772776770	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72819506	TAAAAAGTAAAAGCC[C/T]GTCTTACTACCTCTG	89849
rs772844446	in-del	-/CT	7.56974e-05	0.00615166	frameshift-variant, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822892	GGGAGAGAAGGGAGA[-/CT]CTGGCTCTGGCCCCT	89849
rs772863057	snp	C/T	6.59294e-05	0.00574111	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828422	CCTGAGCCTCAGCCA[C/T]GACCAACTGCACCTG	89849
rs772932290	in-del	-/GAGCCCCAGCCCCACCTCTCCTCCCCACCAGCCAG	7.57074e-05	0.00615207	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826832	GCCTATTGTGAGCCC[lengthTooLong]GAGCCCCAGGCCAGG	89849
rs773019535	in-del	-/AAA			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841342	GAGACTCTGTCTCCA[-/AAA]AAAAAAAAAAAAAAA	89849
rs773062016	snp	A/G	3.36304e-05	0.0041005	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822375	CGCCGGTGTCTGGAA[A/G]GGAGGGGGGCAGCAG	89849
rs773093966	snp	A/G	1.64838e-05	0.00287083	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828475	CACTCAAGGTCATCG[A/G]CCTGCGTGTCAGCAA	89849
rs773135874	snp	G/T	1.74921e-05	0.00295732	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817834	GGAGGAGGAGGAGGG[G/T]CTCCGGCTGGTCTGT	89849
rs773180988	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836798	ATAAATACAAACTTT[C/T]TACAGCCACTGTAAA	89849
rs773238415	snp	C/G/T	4.94567e-05	0.00497255	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826571	CCAGCTCTGGAAGGT[C/G/T]GGGGAGGCACAGTCC	89849
rs773309842	snp	A/G	4.94271e-05	0.00497102	intron-variant	ATG16L2	GRCh38.p7	11:72828821	CAAGTGTGCCCTGCC[A/G]GACCCTGTGTGTGCC	89849
rs773447544	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72834984	GATGCCCTCCCACTG[A/G]GTCTCTGGCTTGTGA	89849
rs773474388	snp	A/G	3.32336e-05	0.00407624	synonymous-codon, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824764	AGGTCACTCAATTGG[A/G]GGAGCCCCTGAGCAG	89849
rs773494642	in-del	-/CCTCTCACTT			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826489	GCCTCCGGCTTAGCA[-/CCTCTCACTT]CCTCTCACTTCCTCT	89849
rs773498117	snp	A/G	0.000161473	0.00898389	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822875	CCTAGGCGATGGGAT[A/G]AGGGAGAGAAGGGAG	89849
rs773556217	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823504	GTCATTGAGGCTGCC[C/T]GCTCTGGGCGCCATT	89849
rs773569322	snp	A/G	6.18857e-05	0.00556228	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841508	TCTTATCTGGGCTGG[A/G]GTAGGGGCTGCTGGG	89849
rs773617764	snp	A/G	4.94279e-05	0.00497107	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824157	TGTGTGCACCCACGT[A/G]TGTGTCGGGCTCCCC	89849
rs773649954	snp	C/T	1.65181e-05	0.00287381	intron-variant	ATG16L2	GRCh38.p7	11:72828709	ACCTCTGTTCTGACC[C/T]CAGCCCTGTCTGTCC	89849
rs773683959	snp	A/T	1.70507e-05	0.00291977	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827144	GTGGGGTGGCTCCCG[A/T]CAACCCTCCTCTGAG	89849
rs773690406	snp	C/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813759	CGTAAACCCTTCTGC[C/T]TCCTGTCCTCCCAGC	89849
rs773691335	in-del	-/GGACGCGGCTAC	4.33717e-05	0.00465661	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814602	GGATGGCGGCTGAGG[-/GGACGCGGCTAC]GGGCGCGGGGAGAGG	89849
rs773776801	snp	G/T	1.69588e-05	0.00291189	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822366	GTCGGGCCTCGCCGG[G/T]GTCTGGAAGGGAGGG	89849
rs773789344	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72833642	CATTCTAGGAAAGGC[C/T]GGGCGAGGTGGCTCA	89849
rs773844965	snp	A/T	1.66101e-05	0.0028818	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825303	CCCTTTCCCCACAGG[A/T]TGCCCACCTCTCTGA	89849
rs773891289	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72830542	TAGTGCAGCCTCAAA[C/T]TCCTGCAGCCTTAAA	89849
rs773912123	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72831375	GTTGGGCATGGTGGC[A/T]CATGCCTGTAATCCC	89849
rs773945981	snp	A/G	1.64732e-05	0.0028699	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842685	TCTTCCACTAGCACC[A/G]ATGGGAAAACTCCAA	89849
rs774000414	snp	A/T	3.29864e-05	0.00406105	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842811	TCATCTGTCTGGCCC[A/T]CATAATCATAAAGTG	89849
rs774009423	snp	C/G/T	9.62428e-05	0.0069364	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822411	CCCTGGAGGAAGGGA[C/G/T]CGGGTCTAGCCCCGC	89849
rs774060355	snp	C/T	0.000126223	0.00794327	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814482	GGTGCCCCCGCAGCG[C/T]GCTGGAAACGCCACA	89849
rs774107286	snp	A/G	1.83199e-05	0.00302648	intron-variant	ATG16L2	GRCh38.p7	11:72829260	CCAGGTTGCAGGCGC[A/G]GTTCCTGAAGCCCCC	89849
rs774169827	in-del	-/TG	1.65446e-05	0.00287612	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828337	GCTGTTCCTCATCCC[-/TG]TCTCTGTCCTTGTTC	89849
rs774231672	snp	A/G	1.6607e-05	0.00288153	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840926	TGCCTTGATGCCTGT[A/G]AGAATCCTGGTGACT	89849
rs774270734	snp	A/G/T	0.000347479	0.0131773	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823762	GCGTCTCTCCTCCCT[A/G/T]TAGGCCCCGGCTCAG	89849
rs774287306	snp	A/G	1.65663e-05	0.002878	intron-variant	ATG16L2	GRCh38.p7	11:72816836	GCCCCTGGTAAGTGT[A/G]TGTGGGTCCGTGGTC	89849
rs774298944	snp	A/C	6.85895e-05	0.00585577	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822040	CGCTCTTTCCGTCCT[A/C]CAGGCTGGCAGCCCT	89849
rs774324084	snp	C/T	1.69717e-05	0.002913	intron-variant	ATG16L2	GRCh38.p7	11:72817745	TGAGCACCACTCTGA[C/T]TGGTTGGCAGGGAGG	89849
rs774330328	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839517	ACGAGGGTACTGGCA[A/G]TAGGGGAAGTAGAGA	89849
rs774334012	snp	A/G			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827392	GGAGGAGTCTTGGTG[A/G]CACTTTGGGCAGGCA	89849
rs774404517	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72833831	GAGAGGCTGAGGCAG[C/G]AGAATCGCTTGAACC	89849
rs774412932	snp	C/G	0.000310994	0.012466	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821583	CGGGCAGGTGAGCAG[C/G]CGACTCCCTTAGCGC	89849
rs774459699	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835119	GACCAAAATTTAGCT[A/G]TGACGCTGGGGTGAG	89849
rs774597347	snp	A/G	8.36155e-05	0.00646535	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826795	CCGCGACCGGACAGT[A/G]AAGGAGTGGGACCTC	89849
rs774601753	snp	A/G	1.65405e-05	0.00287576	intron-variant	ATG16L2	GRCh38.p7	11:72828693	GCAGAGACTAGTGAT[A/G]ACCTCTGTTCTGACC	89849
rs774633244	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72825734	CCCTGAGTCTACCAG[A/G]TGACCCTCTTCTAGC	89849
rs774719029	snp	C/G	0.00041175	0.0143424	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824064	TTTTGTCTCAGGTCT[C/G]CCTCAGCCACCTCCC	89849
rs774746234	snp	G/T	1.64947e-05	0.00287177	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826691	TGATCCGTACCTGGG[G/T]CCGGGGTACAGGAGA	89849
rs774753248	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72817161	TGATGCCTAAAGAAA[A/G]GGTCTTGCTACCTGT	89849
rs774789726	snp	A/G	2.15181e-05	0.00328003	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841443	AGACCCATGCCCAGG[A/G]GAACCCTTACCGTTT	89849
rs774810073	in-del	-/AC	1.64868e-05	0.00287109	utr-variant-5-prime, frameshift-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816794	TGCAGCCGGAGCCAA[-/AC]AGTGTCACTCCCACC	89849
rs774820886	snp	A/G	1.68162e-05	0.00289962	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829346	TACTCCGGGAGCCAC[A/G]TGGTGAGCGTGGACC	89849
rs774830257	snp	G/T	1.64887e-05	0.00287125	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827283	CAGAAGATCCGGTTC[G/T]GGGACAGCAGGTGAC	89849
rs774836252	snp	C/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841958	ATAAAATACTTTGCT[C/G]AATTTCTGACTTCCC	89849
rs774864125	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72824998	CAGCCTGTGGTGGGA[A/G]CCACTCAAGCATGTT	89849
rs774883626	snp	G/T	1.99806e-05	0.00316068	intron-variant	ATG16L2	GRCh38.p7	11:72824885	GGGGCAGTGGTGAGA[G/T]AGTGCAGGCACAGGG	89849
rs774914053	in-del	-/AGCGGGG			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813909	CCATCATCCCCGGAA[-/AGCGGGG]AGCGGGGATTCCTCC	89849
rs774997715	snp	A/T			utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821652	AGCGCCGCCGTGCCC[A/T]CCTGTCCGCCCCCAG	89849
rs774998623	in-del	-/GAA	3.39455e-05	0.00411966	cds-indel, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822508	GGTGTCCCAGGAGCT[-/GAA]GAAGGCTGCCAAGCG	89849
rs775028766	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72820368	CCCCTTTTTAGTCAC[A/G]TTCACCCCTCTCCCC	89849
rs775061033	in-del	-/GG			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823770	CTCCCTGTAGGCCCC[-/GG]GGCTCAGCTTCCCAG	89849
rs775135083	snp	C/T	1.70889e-05	0.00292304	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822529	GGCTGCCAAGCGGAC[C/T]GTGAGCATCAGCGAG	89849
rs775145140	snp	G/T			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828060	ACCCTTCCTTCTCTC[G/T]CTCATATTTTTTAAA	89849
rs775191907	snp	C/T	1.65072e-05	0.00287286	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816735	CTCTCCAGATAACCA[C/T]CTCTTAGAGAAGGCT	89849
rs775212385	snp	A/G			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822461	CCAGGGTCTCAGGAT[A/G]CTTTTTACCCAACAA	89849
rs775225390	snp	A/T	5.09528e-05	0.00504716	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822169	AGGCGCTGCGCGCGC[A/T]CGTCGGGCTCCGGGA	89849
rs775282196	snp	C/T	1.64743e-05	0.00287	synonymous-codon, missense, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842639	AATCTCTCTCATCCA[C/T]GGAGTGTCACCATTT	89849
rs775305654	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72832261	CTTCTCTCCCCCAAA[A/G]CCTTCCCTTCTACTT	89849
rs775329171	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72825032	ATGTGGGCATAAGCC[A/G]GGGAGGGAGAGAGAG	89849
rs775353860	snp	A/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840794	AGTCAGTAACAACAC[A/T]GGGGCCACGGGGAAA	89849
rs775402637	snp	G/T	0.000460003	0.0151588	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822850	TTACCTCTCCTAGGG[G/T]CCCGGACACCCTAGG	89849
rs775420141	snp	G/T	1.87443e-05	0.00306134	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826288	TTGTGCCCTCTCTGA[G/T]CTCCACACTGGGCAG	89849
rs775425827	snp	C/T			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836693	TAAGAAGCATGGGCC[C/T]TTTGGAAAGGTCTGT	89849
rs775449948	snp	C/T	1.65157e-05	0.0028736	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816823	ACCACCCACCAGGGC[C/T]CCTGGTAAGTGTATG	89849
rs775461391	snp	C/T	4.16086e-05	0.00456098	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838919	AGTCAGTTCCTGACT[C/T]AGTATCTGAAGCATC	89849
rs775525969	snp	A/G	0.000194439	0.00985808	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821523	CGCGTCCCTGTGCAA[A/G]GTCCCAAACCTGTGT	89849
rs775543374	snp	C/G	1.64738e-05	0.00286995	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824053	ATCTCTCTTGGTTTT[C/G]TCTCAGGTCTGCCTC	89849
rs775557791	snp	C/T	1.65551e-05	0.00287702	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827185	CTGCTGCTTGGTCCC[C/T]AGGCTCCAGGACCAT	89849
rs775594514	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72825922	GCTGCGTGCTCTACA[C/T]AGTCCCTTCTCCCTG	89849
rs775663297	snp	A/G	1.73721e-05	0.00294716	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840969	TTTTTTCTAAGGGAG[A/G]AAACCAAAGAAGCTC	89849
rs775678649	snp	A/T	1.9121e-05	0.00309195	intron-variant	ATG16L2	GRCh38.p7	11:72817858	GGTCTGTGGTGAGGT[A/T]AGTTGGGAAGGGGTC	89849
rs775750821	snp	C/T	1.67287e-05	0.00289207	intron-variant	ATG16L2	GRCh38.p7	11:72829029	CTGGCCCCAGTCCTG[C/T]CAGGCTGATTCCAGG	89849
rs775795357	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835188	CTCCAGTACCGAAAG[C/T]AGCTTTCACTGGCAG	89849
rs775819315	snp	C/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813319	TCTCCCATCGTTGCC[C/G]AACTTCTCTCGTTCC	89849
rs775864044	snp	A/G	1.64901e-05	0.00287137	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826593	GCACAGTCCAAGGTG[A/G]GGCCTGACTGGGGAG	89849
rs775905348	snp	C/T	3.29468e-05	0.00405861	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828919	GGCAGGCTCCTGTGA[C/T]GGGGCCCTTTACATC	89849
rs775912740	snp	A/C/G	3.29683e-05	0.00405996	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828481	AGGTCATCGACCTGC[A/C/G]TGTCAGCAACATCCG	89849
rs775919368	snp	A/G	3.30055e-05	0.00406222	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826682	CCAAACTCTTGATCC[A/G]TACCTGGGGCCGGGG	89849
rs775994416	snp	A/G	0.000118842	0.0077076	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822361	GAGGAGTCGGGCCTC[A/G]CCGGTGTCTGGAAGG	89849
rs776040735	snp	C/T	5.03318e-05	0.00501631	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827164	CCTCCTCTGAGGCCC[C/T]GGGGTCTGCTGCTTG	89849
rs776156339	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841118	GGCTGCAGTGAGCTA[C/T]GATCCCACCACTGCA	89849
rs776236281	in-del	-/A	1.70721e-05	0.0029216	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826469	TTCTGTGGCCCGAAG[-/A]ATGTTGCCTCCGGCT	89849
rs776260226	snp	A/G	3.33795e-05	0.00408517	intron-variant	ATG16L2	GRCh38.p7	11:72825415	TGTGGGAAGTAAGGA[A/G]CCCTCCCCTGCCGGC	89849
rs776286724	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72817547	TGAGAAGGGTCCTTG[A/G]CCAAGGCCTAGGGGA	89849
rs776290220	in-del	-/CTG			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824517	CCCACCAACCCTACC[-/CTG]CTGCTCCTGTGTCTG	89849
rs776323966	in-del	-/G	4.00176e-05	0.00447294	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822799	GTGCTGGGGTCGGGA[-/G]GGGCTGGCTTGGTCC	89849
rs776367938	snp	A/G	1.67307e-05	0.00289224	synonymous-codon, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824776	TGGGGGAGCCCCTGA[A/G]CAGCGATACCAGATC	89849
rs776433416	in-del	-/TG	3.5979e-05	0.00424125	utr-variant-5-prime, frameshift-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817847	GGGCTCCGGCTGGTC[-/TG]TGGTGAGGTAAGTTG	89849
rs776453643	snp	A/C			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823455	ACCTTGGGTGCCTGT[A/C]CGCAGGGTCTCCTCC	89849
rs776499710	snp	A/G	0.000165631	0.00909881	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843164	ACCACTGGCATCTCC[A/G]TTGAGGCTGCCTGAA	89849
rs776505320	snp	A/C			synonymous-codon, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827213	CATCAATGTCCTTTC[A/C]TACTGTAATGACGTG	89849
rs776507940	snp	C/T	2.04857e-05	0.00320038	intron-variant	ATG16L2	GRCh38.p7	11:72826137	TTTGTGAGGTTAAGA[C/T]CTCATTTCAACTGTC	89849
rs776537598	snp	A/T	3.31978e-05	0.00407404	intron-variant	ATG16L2	GRCh38.p7	11:72828555	CTTTGCTGGGACAGC[A/T]GAGCCTCTCTTCTCC	89849
rs776570024	snp	G/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842064	CTACCTGTCTGGCCT[G/T]CAGTGATAGATCCCT	89849
rs776573775	snp	A/G	0.000118756	0.00770479	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822509	GTGTCCCAGGAGCTG[A/G]AGAAGGCTGCCAAGC	89849
rs776653026	snp	A/T	1.64738e-05	0.00286995	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824039	CAGTCCCTTAGCATA[A/T]CTCTCTTGGTTTTGT	89849
rs776745903	snp	A/G	3.29717e-05	0.00406015	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826575	CTCTGGAAGGTGGGG[A/G]AGGCACAGTCCAAGG	89849
rs776775518	snp	A/T	5.0391e-05	0.00501926	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840947	CCTGGTGACTCAGCA[A/T]GAAGGCTTTTTTCTA	89849
rs776932302	snp	A/G	3.37376e-05	0.00410703	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817760	TTGGTTGGCAGGGAG[A/G]AGTCAGAGCTTGACT	89849
rs776932794	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72826018	AGGTGTAGTCTCCAG[C/T]CCAGGCCCGCAGAAC	89849
rs776933053	snp	A/G	2.74194e-05	0.00370256	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841595	AGATCTGCAGCAAAG[A/G]GAAGCGAGGTTACCC	89849
rs776986374	snp	A/C	1.64846e-05	0.0028709	intron-variant, splice-acceptor-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842615	ACTGTCTCCCCTCTC[A/C]GGTACCTGAATCTCT	89849
rs777038938	snp	C/T	7.31021e-05	0.0060453	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822052	CCTCCAGGCTGGCAG[C/T]CCTGGAGGCCCGCGT	89849
rs777092904	snp	C/G			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827036	TGTGGGTAGGAAAAA[C/G]ACGTGGGTGAGCCCT	89849
rs777118716	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72833742	CCTGGCCAACATGGT[A/G]AAACCCCGTTTCTAC	89849
rs777150258	snp	C/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813035	GAAGCTTGAACTCAG[C/T]GTAGGGGCAGGAAAG	89849
rs777159584	snp	A/G			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815318	CTCTCACTGGGGCTA[A/G]TCTTGGCCAAACCCC	89849
rs777175160	snp	A/C	0.0016116	0.0283409	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822151	TGCAGCGGGCAGCCT[A/C]CGAGGCGCTGCGCGC	89849
rs777215909	in-del	-/AG	5.08643e-05	0.00504277	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840867	TAATCCTGCAAGATC[-/AG]AGACTTACAGGTCGC	89849
rs777243635	snp	A/G			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821753	GCAGGTGAGGCGCGG[A/G]CGGGGGCGGGAGGGA	89849
rs777247190	in-del	-/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829527	GGCAGGACCTGGCCT[-/G]TTTGTTTAAAAATGA	89849
rs777264141	snp	G/T	2.07359e-05	0.00321986	intron-variant	ATG16L2	GRCh38.p7	11:72826124	CCAATTCCTCCATTT[G/T]GTGAGGTTAAGACCT	89849
rs777293453	snp	C/T	1.6495e-05	0.0028718	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816807	AAACAGTGTCACTCC[C/T]ACCACCCACCAGGGC	89849
rs777366428	snp	C/T	2.25253e-05	0.00335591	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822590	GCGTTCTGCCTCCCG[C/T]CCCGCCTGCCTGCGG	89849
rs777392140	snp	C/T	1.69795e-05	0.00291367	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826218	GAGCTGGTGGCAGCA[C/T]CACCAGTGTGGACTT	89849
rs777416264	snp	G/T	1.83078e-05	0.00302549	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822976	GGTGAGGACCCAGGT[G/T]ACAGTCTCAGAGCTC	89849
rs777437660	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837547	TTCTACAGGAGCGGA[C/G]AGCAGACAGTCAGCA	89849
rs777470467	snp	C/G	1.65244e-05	0.00287436	intron-variant, missense	ATG16L2	GRCh38.p7	11:72824723	CCTGACCCCAACCCA[C/G]CTTACCCCAGTTTTA	89849
rs777517782	snp	A/G	1.65745e-05	0.00287871	intron-variant	ATG16L2	GRCh38.p7	11:72828549	TGTGGCCTTTGCTGG[A/G]ACAGCTGAGCCTCTC	89849
rs777531815	snp	C/T	0.000182899	0.00956117	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821780	GGGACCGCGCCCACC[C/T]CAGGGAGGCCCGGGG	89849
rs777604074	snp	C/G/T	8.70386e-05	0.00659642	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841435	ATGCATTTAGACCCA[C/G/T]GCCCAGGAGAACCCT	89849
rs777607093	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72833103	CCTTGGTCATCTCTC[A/T]GTCCCTGGCTTCAGT	89849
rs777627260	snp	C/T	0.000162836	0.00902171	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838760	CAAGCCTGGCCTTGA[C/T]TGTAGCAGTAATGGA	89849
rs777671771	snp	A/C	0.000385282	0.0138742	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821515	AACAGCAGCGCGTCC[A/C]TGTGCAAGGTCCCAA	89849
rs777734621	snp	A/G	1.64735e-05	0.00286993	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828897	GCCCGGACAGAAGCT[A/G]TGCACTGGCAGGCTC	89849
rs777762854	snp	A/C	0.000391389	0.0139836	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822305	GGAGCGGTGAGGGAG[A/C]AGGCCCCGCCCCTCC	89849
rs777798669	snp	C/G	2.17663e-05	0.00329889	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841553	ACGGCAGTGGAGGCA[C/G]GGAGGCGTGTGGCTT	89849
rs777862692	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842717	ACGCCCATTGAATTC[C/T]CCTTCCCAGAAGCCA	89849
rs777901428	snp	A/G	3.84623e-05	0.00438516	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822128	GGAGTGGCGGGCGCA[A/G]AATGCGGTGCAGCGG	89849
rs777937554	in-del	-/CTGCCTC			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822579	TCCGACCCTTGCGTT[-/CTGCCTC]CTGCCTCCCGCCCCG	89849
rs777977970	in-del	-/C	5.09359e-05	0.00504632	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822394	GGGGGGCAGCAGCCG[-/C]CCCCTGGAGGAAGGG	89849
rs778016494	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72818643	AATCCTTCACAACTT[C/T]ATGGTTGTAGAGGAG	89849
rs778057497	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829611	CTCACTTTTTCTCCC[A/G]AAGTAGAAAAAAATG	89849
rs778083614	in-del	-/GAG	4.95626e-05	0.00497784	cds-indel, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824743	CCCCAGTTTTAAGAA[-/GAG]GAGAGGTCACTCAAT	89849
rs778168203	snp	C/T	1.71413e-05	0.00292752	intron-variant	ATG16L2	GRCh38.p7	11:72816878	CCTGTGCTGGGGCCC[C/T]GCCCCTGCTGCCTGT	89849
rs778251705	snp	A/T	3.3552e-05	0.00409571	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838900	AACAATTACGTAGTT[A/T]GTCAGTCAGTTCCTG	89849
rs778252927	snp	C/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836262	TCCATCCACCCCTGG[C/G]ACCGAGAAAATCTCC	89849
rs778279430	snp	C/T	1.8176e-05	0.00301458	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824841	GGGCTCAGGATGTGC[C/T]GGTAAGGGAGGAGCT	89849
rs778295388	snp	G/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824359	AAGGTCGTCACAGGG[G/T]ACCAAGAGCTCCAGC	89849
rs778340234	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72832221	GCTCAGGAAATGGTC[G/T]GACTGATCTCTGGGA	89849
rs778361922	snp	C/G	3.32138e-05	0.00407502	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827328	GGAGGACTTGGGGAG[C/G]GCTGGGGACAGGGCT	89849
rs778386612	in-del	-/TTAT			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815973	CTGGGGAAGTTGGGA[-/TTAT]TTATTTATTTATTTA	89849
rs778394806	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72818021	CTGAGCAGGGGTCAG[A/T]GTGCCCTGGGCAGCC	89849
rs778439980	snp	A/G	0.0001493	0.00863872	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825378	CTGGAGGGGCTGACC[A/G]CCTGATCCACCTCTG	89849
rs778469920	in-del	-/TTTTCTTTTCTTTT			intron-variant	ATG16L2	GRCh38.p7	11:72819751	TTTTTCTTTTCTTTC[-/TTTTCTTTTCTTTT]TTTTTTTTTTTTGAG	89849
rs778474685	snp	A/C	3.3588e-05	0.00409791	intron-variant	ATG16L2	GRCh38.p7	11:72825450	TTGGTGCTTCTCTCC[A/C]GACCCTCTCCTCAGC	89849
rs778586469	snp	C/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813123	TCCAAACATCAGGCT[C/T]GGCCTGTGCAAAGGC	89849
rs778655386	snp	C/T	1.87064e-05	0.00305825	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841008	TGAGTTGTTGAGCAA[C/T]AATGCTGATGCAAGG	89849
rs778762765	snp	A/G	3.52989e-05	0.00420098	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843130	GTGACCAAATAAAGA[A/G]TGCCTTGTTTCAGTC	89849
rs778767910	snp	A/T	1.65072e-05	0.00287286	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826653	GGACTAGGGGGCCTG[A/T]TATGGGGTCTTGGCC	89849
rs778888175	snp	C/T	2.30944e-05	0.00339804	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841567	AGGGAGGCGTGTGGC[C/T]TGGGGGAAGGAGAGA	89849
rs778941737	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72833264	ATCAGACGTGGACCC[A/G]TCTGTGAGATTCAGA	89849
rs778942205	snp	A/G	1.71246e-05	0.00292609	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817827	AGTGGCAGGAGGAGG[A/G]GGAGGGGCTCCGGCT	89849
rs778946816	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72833208	TGGGGCAGCACATTT[C/G]CTGAATTGAATAGAG	89849
rs778956881	snp	A/G	1.64732e-05	0.0028699	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824092	CCCTGACGCTGTCCC[A/G]CTGTGTGGATGTGGT	89849
rs778991084	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72830960	TGAGTGCATCTCAGA[C/T]ATGCTTTTCTTTCTT	89849
rs779035627	snp	C/G			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829717	ATCCAGGCTTGGCCC[C/G]CTTCCTCCTTCCATA	89849
rs779071640	snp	C/T	3.56513e-05	0.00422189	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822100	CGCGGGCGCAGCAGG[C/T]CCAGCAGGTGGAGGA	89849
rs779077489	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72818147	CACTACTCCATGGCT[C/T]ACCCCTCGCCCAGCC	89849
rs779108506	snp	C/G	6.16884e-05	0.00555341	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822273	GCGGCCGAGCGCAAC[C/G]TGCGCAACGAGCGCC	89849
rs779191349	snp	C/T	1.6757e-05	0.00289452	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814605	TGGCGGCTGAGGGGA[C/T]GCGGCTACGGGCGCG	89849
rs779305377	snp	C/G/T	5.02021e-05	0.00500984	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838858	TTCTGTGTAGGTGGA[C/G/T]GGGGAGCTGCCCGGA	89849
rs779307457	snp	C/T			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827063	CCCTGTGCTGGGAAG[C/T]GGAAGACCTGGGTTC	89849
rs779378328	snp	G/T	2.20378e-05	0.0033194	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822577	CGGTCCGACCCTTGC[G/T]TTCTGCCTCCCGCCC	89849
rs779400435	in-del	-/C	3.29495e-05	0.00405877	intron-variant	ATG16L2	GRCh38.p7	11:72828847	TGCCCTCCCCTCTGA[-/C]CCCCCCGTTTTCTTG	89849
rs779406833	snp	A/C/T	3.42743e-05	0.00413959	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827142	CTGTGGGGTGGCTCC[A/C/T]GACAACCCTCCTCTG	89849
rs779474862	in-del	-/A	1.69384e-05	0.00291014	intron-variant	ATG16L2	GRCh38.p7	11:72825254	CGTGAGCACTCACAG[-/A]GACATGCGCGGGGAG	89849
rs779488163	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823404	AAGCATGTGTAGATG[C/T]GTGCTCACACTTGTG	89849
rs779505229	snp	A/G	1.65789e-05	0.0028791	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840912	AGGTCTCAGGAGTAT[A/G]CCTTGATGCCTGTGA	89849
rs779506320	snp	C/G	1.64844e-05	0.00287087	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828455	CAGCTGTTCCCGAGA[C/G]AACACACTCAAGGTC	89849
rs779638371	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72833363	ATCTGTACATTACCC[C/T]ATTTCATCCTCCTGG	89849
rs779676341	snp	A/G	1.70342e-05	0.00291836	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817822	GGTGAAGTGGCAGGA[A/G]GAGGAGGAGGGGCTC	89849
rs779764714	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842292	TACTACGTAAATTAA[C/T]CACAGAGCAACGCCT	89849
rs779767714	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72834294	AGGGCTGGGCAGTCA[C/T]TGGCCACAAAACCAA	89849
rs779813565	snp	C/T	0.00216684	0.032844	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823568	GCAGGTCCCTGGTGT[C/T]CAGGCCTTGGGGCAG	89849
rs779945229	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72825219	CAGGCTGTGTCTGCA[C/G]AGGCACCGGTAAGAG	89849
rs779983317	snp	G/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840389	CAAGTTATGACCTTG[G/T]AGTACAGTGGTGGGT	89849
rs780009142	snp	C/T			missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824094	CTGACGCTGTCCCAC[C/T]GTGTGGATGTGGTGA	89849
rs780039646	snp	A/C	1.6498e-05	0.00287206	stop-gained, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826544	TTTAGCAGCAACTTA[A/C]AACCAGGCTGCCCAG	89849
rs780097225	snp	A/T	1.65034e-05	0.00287253	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826632	GAGGTCAGAGGTCAT[A/T]CCTCAGGACTAGGGG	89849
rs780101920	snp	C/T	3.32591e-05	0.0040778	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826786	GACTGGGAGCCGCGA[C/T]CGGACAGTGAAGGAG	89849
rs780105120	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72819271	TCATGTTGACTCTAT[C/G]TCCAAATCCATCAAT	89849
rs780130741	snp	C/G			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820660	CAGTGCAGGTGGCAG[C/G]GCCAACCGTGCTCCT	89849
rs780150270	snp	A/G	8.2373e-05	0.00641714	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824021	ATTTGTACACACACC[A/G]GCCAGTCCCTTAGCA	89849
rs780155191	snp	C/T	1.64741e-05	0.00286998	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824138	GTAAGTGTGTGTGTG[C/T]CTGTGTGTGCACCCA	89849
rs780156782	snp	A/G	0.000175293	0.00936032	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826874	CCAGCCAGGAGCCCC[A/G]GGCCAGGGCACAAGG	89849
rs780207822	snp	A/G	1.6525e-05	0.00287441	missense, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824744	CCCAGTTTTAAGAAG[A/G]GGAGAGGTCACTCAA	89849
rs780224312	snp	A/C			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827679	CGTGGTGGCTCATAC[A/C]TGTAATCCCAGCTGT	89849
rs780230005	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838031	GCTAATTTCAGATCC[A/G]GAAGTTCCATTTCTG	89849
rs780267490	snp	A/G	4.9731e-05	0.00498629	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825368	CTCCTGGCCACTGGA[A/G]GGGCTGACCGCCTGA	89849
rs780485692	snp	C/T	2.06913e-05	0.0032164	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841492	AAGTACAGGGAGCTC[C/T]TCTTATCTGGGCTGG	89849
rs780506741	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72835983	AAACTCCTGACCTCA[A/C]GTGATCTGCCCGCCT	89849
rs780531630	snp	A/C/T	1.64974e-05	0.00287201	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828368	CCTCAGGGGGCCCCA[A/C/T]TGCACCCAGGTCATC	89849
rs780550050	snp	C/T	5.04936e-05	0.00502436	synonymous-codon, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829336	GGCCTGGTGCTACTC[C/T]GGGAGCCACATGGTG	89849
rs780553708	snp	C/T	4.03584e-05	0.00449194	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822803	TGGGGTCGGGAGGGG[C/T]TGGCTTGGTCCCTTG	89849
rs780616416	snp	A/G	3.52491e-05	0.00419801	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822406	CCGCCCCCTGGAGGA[A/G]GGGACCGGGTCTAGC	89849
rs780653733	snp	C/G	3.31768e-05	0.00407275	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840901	TTTGCCATATGAGGT[C/G]TCAGGAGTATGCCTT	89849
rs780712339	in-del	-/CTTCCTTC	1.8553e-05	0.00304568	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829439	GCCCGAAGCCTGAAG[-/CTTCCTTC]GGCGCCATGCAGGGG	89849
rs780738066	snp	A/G	1.65018e-05	0.00287239	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826539	CAGGTTTTAGCAGCA[A/G]CTTACAACCAGGCTG	89849
rs780838487	snp	A/C	1.6793e-05	0.00289763	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817805	TCACTGGTCGCACTG[A/C]GGGTGAAGTGGCAGG	89849
rs780840366	snp	C/G	4.94556e-05	0.00497246	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827276	CAATGACCAGAAGAT[C/G]CGGTTCTGGGACAGC	89849
rs780909362	snp	A/G	1.759e-05	0.00296558	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822084	GCGCAGCTGCGAGAG[A/G]CGCGGGCGCAGCAGG	89849
rs780925969	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72834818	TCAAACTCCTGATCT[C/G]AGGTGATCCACCAGC	89849
rs781020374	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72831232	CTTATTCAGGCTGGA[A/T]GCGGTGGCTCACGCC	89849
rs781107228	snp	A/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812677	AGCCAGGCCAAGCCC[A/T]GTTAATATACTCTCC	89849
rs781119624	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815254	CGCACCTCTGGCCGC[C/T]TGCGATTGTATGTCT	89849
rs781159430	snp	A/G	1.64746e-05	0.00287002	intron-variant	ATG16L2	GRCh38.p7	11:72828789	CAGGTATGTCCGTGA[A/G]AGCATATGCCTGTGT	89849
rs781221620	snp	C/T	3.314e-05	0.00407049	intron-variant	ATG16L2	GRCh38.p7	11:72829002	GAGCATGGCCTCCAC[C/T]TGGCCACCTGCCTGG	89849
rs781272626	snp	C/G	1.65064e-05	0.00287279	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826672	GGGGTCTTGGCCAAA[C/G]TCTTGATCCGTACCT	89849
rs781276437	snp	C/T	3.37849e-05	0.00410991	synonymous-codon, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829318	CGCTGCCGTCAACGC[C/T]GTGGCCTGGTGCTAC	89849
rs781308425	in-del	-/G	1.75108e-05	0.0029589	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822354	CTGCAGGGAGGAGTC[-/G]GGCCTCGCCGGTGTC	89849
rs781326474	snp	C/T	4.98277e-05	0.00499113	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826781	GCAGTGACTGGGAGC[C/T]GCGACCGGACAGTGA	89849
rs781350411	snp	G/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839277	AGTTGTGAAGGGCCT[G/T]GTTAAACCATGTTTA	89849
rs781407047	snp	A/G	0.000116137	0.00761939	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828317	GTCAGGAGTGGCCTG[A/G]CTAGGCTGTTCCTCA	89849
rs781444879	snp	A/C	4.44435e-05	0.00471378	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814576	CCTGTGAGTGCGCCC[A/C]GGTGCTGAGAGGATG	89849
rs781477083	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840480	CCCGGAGAATAAACG[C/T]TCTTTAAGGCCATGA	89849
rs781517248	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72828610	CCCTGGAGGCCCCTC[A/C]AGACCAGGTCCTGCT	89849
rs781568852	in-del	-/G			intron-variant	ATG16L2	GRCh38.p7	11:72820498	CATAAATGAAAGCAA[-/G]TGACAAGTGAGAAAG	89849
rs781655286	snp	C/G	1.64833e-05	0.00287078	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828448	ACCTGCTCAGCTGTT[C/G]CCGAGACAACACACT	89849
rs781671946	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72817937	GTACTCCTGTGTTTG[C/T]TGAATTCTCCAAGCC	89849
rs781689013	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841169	TAATACCCTTTGTCC[A/G]GAAAAAATACAAAAA	89849
rs781724178	snp	C/T	1.67049e-05	0.00289002	intron-variant	ATG16L2	GRCh38.p7	11:72825284	GGGCCGGGGCACCAA[C/T]CTCCCCTTTCCCCAC	89849
rs781745820	snp	A/T	1.75477e-05	0.00296202	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822352	CCCTGCAGGGAGGAG[A/T]CGGGCCTCGCCGGTG	89849
rs781750008	snp	C/G	1.65712e-05	0.00287843	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825363	GCAGCCTCCTGGCCA[C/G]TGGAGGGGCTGACCG	89849
rs781752775	snp	A/G	1.6476e-05	0.00287014	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842760	TTTTCTTTGTTCAAG[A/G]TACGGATTATTGCTC	89849
rs781765879	snp	C/T	9.23617e-05	0.00679502	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822395	GGGGGCAGCAGCCGC[C/T]CCCTGGAGGAAGGGA	89849
rs796216909	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72826072	ACCTGGGGATGTGTC[A/G]GGGGGTGGGGCGGGA	89849
rs796335435	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837466	ATTTCTTAACCAAGG[-/A]AAAAAAAAAAAAACA	89849
rs796488576	in-del	-/AAG			cds-indel, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838001	AATACCCAAATACAA[-/AAG]AACATTATATTGGCT	89849

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