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
rs891655	snp	A/G	0.0681886	0.171594	intron-variant	ATG16L2	GRCh38.p7	11:72817928	AATTCAGCAAACACA[A/G]GAGTACCCGTCACTG	89849
rs891657	snp	G/T	0.0150606	0.0854603	intron-variant	ATG16L2	GRCh38.p7	11:72829180	CCTGTGAGCTAACTT[G/T]ACAGATGAGGAAACA	89849
rs919600	snp	C/T	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72818748	TATAGCAACTGTCAA[C/T]AGATGTTGAGAGAAT	89849
rs1045315	snp	C/G	0	0	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841516	ACCAGCCTCCCAGCA[C/G]CCCCTACCCCAGCCC	89849
rs1045372	snp	A/C	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836863	ATGGAATCCAGCACC[A/C]CAGTGCACAGGTCAG	89849
rs1062909	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838452	CAGTCCCTAAATTAC[G/T]GATCATGTGCACTCG	89849
rs1062910	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838373	TCTTCAAGTGGCTTT[G/T]GCTCATCTGATTGAG	89849
rs1126205	snp	A/C	0.379942	0.213577	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812749	TCCCTTTAGAACTGG[A/C]GGACTCTTGGGTGCT	89849
rs1298094	snp	A/C	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838251	AGTCCAATTTTTCCC[A/C]ATAAGGTTTCACTTT	89849
rs1320730	snp	A/T	0	0	intron-variant	ATG16L2	GRCh38.p7	11:72817678	CTTGTTTTAGGCTTT[A/T]CATGTAGCATCACTT	89849
rs1801886	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838230	AAATTGGACTGCCCT[G/T]AATTTAGCACCAATT	89849
rs1807188	snp	A/G	0.00335007	0.0407899	intron-variant	ATG16L2	GRCh38.p7	11:72817223	ATAGGTTGGGGCTCA[A/G]AGTTGGGAGGTGCTT	89849
rs1808621	snp	C/T	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72817364	GGGTGGTGGTGCACG[C/T]TCCAGGAGGCTGAGG	89849
rs1864651	snp	G/T	0.0108365	0.0728068	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821524	GCGTCCCTGTGCAAG[G/T]TCCCAAACCTGTGTG	89849
rs1864652	snp	G/T	0.000271186	0.0116413	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821576	AAGGGGGCGGGCAGG[G/T]GAGCAGCCGACTCCC	89849
rs2282613	snp	C/T	0.495351	0.0479864	intron-variant	ATG16L2	GRCh38.p7	11:72819151	AATGAGGTGGGCTGT[C/T]CTTCCTGTCTTCCTG	89849
rs2303969	snp	A/G	0.477684	0.103247	intron-variant	ATG16L2	GRCh38.p7	11:72825227	GTCTGCACAGGCACC[A/G]GTAAGAGGGCCCGTG	89849
rs3214595	in-del	-/C	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72825523	TCTATCTGGAATATT[-/C]TGTGGGCAGTGACTA	89849
rs3765638	snp	A/G	0.331874	0.236213	intron-variant	ATG16L2	GRCh38.p7	11:72826027	CTCCAGCCCAGGCCC[A/G]CAGAACAGACCCAGC	89849
rs3814729	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838441	AATATACTGTACGAG[C/T]GCACATGATCAGTAA	89849
rs3862793	snp	C/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827096	GTCTTGGGAGGACAC[C/T]GGGTTCTGGGCCTCA	89849
rs3862794	snp	A/G	0.38821	0.208322	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827555	ATAAAAGTGGTAACT[A/G]AATGGAAAAAGGTAC	89849
rs3862795	snp	A/G	0.00755907	0.0610114	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827661	GCAAAGCTAGAGGCC[A/G]GGCGTGGTGGCTCAT	89849
rs4245436	snp	C/T	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72816279	GCCACCGCGCCCGGC[C/T]GGGGATTATTTTTAA	89849
rs4944014	snp	C/T	0.403334	0.197456	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816135	AGGCGCCTGCCACCA[C/T]GCCTGGCTAATTTTT	89849
rs4944806	snp	A/G	0.00557542	0.0525036	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822666	CCCCCATGTGGTCGG[A/G]GCCCACGAGACACCT	89849
rs4944808	snp	A/G	0.00279162	0.0372561	intron-variant	ATG16L2	GRCh38.p7	11:72834218	GAAAAACAACTTCAC[A/G]ATGAACAAAATAAAT	89849
rs6592491	snp	A/G	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72831487	TCTAGCCTGGGCAAC[A/G]AGAGTGAAACTCCAT	89849
rs6592492	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837551	ACAGGAGCGGACAGC[A/G]GACAGTCAGCACCTG	89849
rs7110183	snp	C/T	0.221439	0.248363	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839990	gaggaagaaagcaaa[C/T]gaggcaaatgtagAG	89849
rs7120156	snp	A/C	0.0770498	0.180522	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821088	ACTCACATTCCCCTG[A/C]CCAGCCTGGAGGGTG	89849
rs7924575	snp	C/T	0	0	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815140	GCTGGTGGATGCTGG[C/T]TGAGCCCAGCGAAGT	89849
rs7936074	snp	C/T	0.0130921	0.0798413	intron-variant	ATG16L2	GRCh38.p7	11:72831642	AGCAGCCACCAGGGG[C/T]CACCAGCTGCCTAGT	89849
rs7939267	snp	A/G	0.0792508	0.182605	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815291	GGAAGTCTAACCACA[A/G]TCCCTGCGGCTCTCT	89849
rs7940683	snp	C/T	0.0444908	0.142359	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842035	CAAGATCGGCAAACA[C/T]GTTCCTTCTTCCTCT	89849
rs7950432	snp	A/C	0.00716266	0.059414	intron-variant	ATG16L2	GRCh38.p7	11:72832256	GAGCCCTTCTCTCCC[A/C]CAAAACCTTCCCTTC	89849
rs10751215	snp	C/T	0.489142	0.0728777	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815042	CTCAGGCTCTGCCGC[C/T]GACAGGCGACGCTGG	89849
rs10751216	snp	C/T	0.489259	0.0724914	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815078	GCTTATGGAACACCT[C/T]CCTGTCAGCCTACCC	89849
rs10898880	snp	A/C	0.48955	0.071525	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814066	AGCACCAGCGGCTCT[A/C]GAACTCGGCCCGGGC	89849
rs10898881	snp	A/G	0.492037	0.0625946	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815973	GCTGGGGAAGTTGGG[A/G]TTATTTATTTATTTA	89849
rs10898882	snp	C/G	0.00716266	0.059414	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827899	GATTGCGCCACTGCC[C/G]TCCAGCCTGGGCGAC	89849
rs10898883	snp	A/C	0.0955749	0.196603	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72827957	AAACCAAAACCAAAA[A/C]CAAAACAAAACAAAA	89849
rs11235600	snp	C/T			utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814494	GCGCGCTGGAAACGC[C/T]ACATCGTGCGGCAGC	89849
rs11235601	snp	G/T	0.426478	0.186327	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814897	CGGGCAGTCCCCGGG[G/T]TAGGGGCTTGATCAG	89849
rs11235602	snp	C/T	0.00716266	0.059414	intron-variant	ATG16L2	GRCh38.p7	11:72820427	TAATCTGTTTTCCAC[C/T]TCTACTACTTGAATT	89849
rs11235603	snp	C/T	0.00179026	0.0298651	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821663	GCCCACCTGTCCGCC[C/T]CCAGATGGCCTACCA	89849
rs11235604	snp	C/T	0.0136909	0.0815967	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822491	AGGGCCAAGCAGGCG[C/T]GGGTGTCCCAGGAGC	89849
rs11235605	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72834725	gtagctgggattaca[C/G]gtacccaccaccaca	89849
rs11430316	in-del	-/T	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72834897	CCATCATTCCATTCC[-/T]TTTACAATTGAGGAT	89849
rs11600601	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72819877	cagcctcccgagtag[C/T]tgggactacaggcgc	89849
rs11602724	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72819898	ctacaggcgcccgcc[A/C]ccatgcccggctaat	89849
rs11604683	snp	C/T	0.172674	0.237741	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827501	TGGCTCTTGGTCCAA[C/T]GCTGGACTCCGCCTG	89849
rs11605818	snp	A/G	0.0119091	0.0762411	intron-variant	ATG16L2	GRCh38.p7	11:72835207	TTTCACTGGCAGGGA[A/G]GTCAGAAGACGGAAA	89849
rs11824212	snp	C/T	0.0825414	0.185628	intron-variant	ATG16L2	GRCh38.p7	11:72831337	catagtgaaaccttg[C/T]ctctactaaaaatac	89849
rs12271465	snp	C/T	0.0138799	0.0821421	intron-variant	ATG16L2	GRCh38.p7	11:72819186	TGCCCCCCAGTCGTT[C/T]TCACACATGCTGGAA	89849
rs12293084	snp	A/G	0.0126979	0.078662	intron-variant	ATG16L2	GRCh38.p7	11:72829233	TACCCAGGTCCAGCA[A/G]TCGGGGCAGAGCCAG	89849
rs12794689	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72825122	GCAGGGGTCCAGGCA[G/T]AGGTGAGAACACCTG	89849
rs12808532	snp	C/T	0.0246875	0.108325	splice-acceptor-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840960	CATGAAGGCTTTTTT[C/T]TAAGGGAGAAAACCA	89849
rs34006101	in-del	-/G			intron-variant	ATG16L2	GRCh38.p7	11:72835798	TGTTCCCCAGACTGG[-/G]AGTGTAATGGCACAA	89849
rs34065651	in-del	-/A			intron-variant	ATG16L2	GRCh38.p7	11:72830523	GAGACACACAAAAAA[-/A]CCTTAGTGCAGCCTC	89849
rs34132493	in-del	-/A			intron-variant	ATG16L2	GRCh38.p7	11:72825834	CTGGAGAGGGGGTGT[-/A]CCTGGGGAGTCAGAG	89849
rs34325800	in-del	-/T			intron-variant	ATG16L2	GRCh38.p7	11:72817400	TAATATTTGTATTTT[-/T]AGTAGAGACGGGGTT	89849
rs34384997	in-del	-/A			intron-variant	ATG16L2	GRCh38.p7	11:72830597	CCTGGTCTTCCCGAA[-/A]GGGCTGGGATTACAG	89849
rs34683629	in-del	-/CATT/CATTCATT	0	0	intron-variant	ATG16L2	GRCh38.p7	11:72830803	ATTCATTCATTCATT[-/CATT/CATTCATT]TACTCATTTAGAGAT	89849
rs34696027	snp	G/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823011	CTGAGCCCCACCCCA[G/T]AGGCTGCCAGGGTCT	89849
rs34732465	in-del	-/T	0.499968	0.00399348	intron-variant	ATG16L2	GRCh38.p7	11:72833932	AATTTTTTTTTTTTT[-/T]CAGGAAAATATTCCC	89849
rs34789461	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837346	TACTTTTGGTCAAAA[-/A]TCCCATGGGGACATT	89849
rs34976675	in-del	-/G			intron-variant	ATG16L2	GRCh38.p7	11:72831684	TTCCCGTTTCCAGGG[-/G]ACACATGGCTGGGGA	89849
rs35220889	in-del	-/C			intron-variant	ATG16L2	GRCh38.p7	11:72833072	CAGATGCCCCTATCC[-/C]TGTGCTCCTACTGCC	89849
rs35333793	in-del	-/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842134	TAAAGGCTGTTTCCC[-/C]TGTGATGAACTAAGT	89849
rs35388270	in-del	-/G			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815115	GGGGGCATCAGGGGG[-/G]CCCCGGGCTGCTGGT	89849
rs35407315	in-del	-/GTCT	0.319856	0.240042	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828155	AGCTTTCAAATCAAA[-/GTCT]GTCTAAGTTCCTCGA	89849
rs35499071	in-del	-/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840268	ACTCAATACATATTT[-/T]GCTGAATGAATGAAG	89849
rs35634761	in-del	-/G			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828243	CCCCAGCGATCCAGG[-/G]CCCTGGGGTTCCTCC	89849
rs35740958	snp	A/G	0.00118199	0.0242817	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826801	CCGGACAGTGAAGGA[A/G]TGGGACCTCGGCCGT	89849
rs35868740	snp	C/T	0.00199481	0.0315187	intron-variant	ATG16L2	GRCh38.p7	11:72819814	ACAGTCGCGTCATCT[C/T]GGCTCGCTGCAACCT	89849
rs56060052	snp	G/T	0.020002	0.0979842	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836507	CGTATTTCTTTTTTT[G/T]CCCATGGGAAAAGCA	89849
rs56071001	snp	A/C	0.105924	0.204309	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827939	TGTCTCAAAACAAAA[A/C]CAAAACCAAAACCAA	89849
rs56088156	snp	C/T	0.00914312	0.0669923	intron-variant	ATG16L2	GRCh38.p7	11:72832523	GCGGGAAGGCTGTTC[C/T]TCCCTCCAGCCTCTT	89849
rs56148078	snp	A/C	0.275999	0.248644	intron-variant	ATG16L2	GRCh38.p7	11:72818313	TCTTGGCTTCTCTTT[A/C]ACCATGCTCTCCTGG	89849
rs57674996	in-del	-/ATCT			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829594	TTTTTATCTCTATCT[-/ATCT]CCTCACTTTTTCTCC	89849
rs58682117	snp	C/T	0.34526	0.23114	intron-variant	ATG16L2	GRCh38.p7	11:72819955	TTTCACCATGTTAGC[C/T]AGGATGGTTTTGATC	89849
rs58718333	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813592	TCTGGCCCTGAGTCA[A/G]GATGCTGGGGTGCTG	89849
rs59059938	snp	C/T	0.0825414	0.185628	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840778	CATCCTTGTTTGGCA[C/T]AGTCAGTAACAACAC	89849
rs59348649	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816237	CGCCCGCCTCGGCCT[C/T]CCAGAGCGCTGGGAA	89849
rs59748827	in-del	-/A			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841364	AAAAAAAAAAAAAAA[-/A]GCAAATGCAGTTTTT	89849
rs60091261	in-del	-/A			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841341	GAGACTCTGTCTCCA[-/A]AAAAAAAAAAAAAAA	89849
rs61049260	snp	C/T	0.0387552	0.1337	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841137	CCCACCACTGCACTC[C/T]AGCCTGGGTGACAGA	89849
rs61348171	snp	A/C			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815568	GAGAGATCTGGAGGG[A/C]TGAAATCAGACTGAA	89849
rs61738587	snp	A/G	0.00314142	0.0395075	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825333	AGGTCAATGCTGTTC[A/G]TTTTGGCCCCAACAG	89849
rs61894254	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814947	GCAGTGAAAGAACGC[A/G]GGACTTGTCCAGAGC	89849
rs61894255	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72834601	TTTTTTTTTTTTTTG[G/T]AGACAGAGTCTTGCT	89849
rs61894256	snp	A/G	0.5	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837464	TGATTTCTTAACCAA[A/G]GAAAAAAAAAAAAAA	89849
rs67634043	in-del	-/ATTC			intron-variant	ATG16L2	GRCh38.p7	11:72830789	TTTCCTTGCTATTCA[-/ATTC]TTCATTCATTTACTC	89849
rs71062791	in-del	-/CTCACCACCACCTCTC	0	0	intron-variant	ATG16L2	GRCh38.p7	11:72835437	TCACCACGAACTCTT[-/CTCACCACCACCTCTC]CTCACCACCACCTCT	89849
rs71477744	snp	C/G	0.00517822	0.0506191	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823911	GATCTGGGTCACCCT[C/G]GTCTCCTGATCTTGG	89849
rs71477745	snp	C/T	0.00478085	0.0486577	intron-variant	ATG16L2	GRCh38.p7	11:72834129	GAAACTTAAAAGTTG[C/T]AGGATTTGGGGATAA	89849
rs71477746	snp	A/G	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72835439	AGGTGGTGGTGAGGA[A/G]AGGTGGTGGTGAGAA	89849
rs71477747	snp	C/T	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72835833	AGCTCACCGCAACCT[C/T]TGCCTCGCAGGTTCA	89849
rs72969813	snp	C/G	0.0293117	0.117459	intron-variant	ATG16L2	GRCh38.p7	11:72828842	TGTGTGTGCCCTCCC[C/G]TCTGACCCCCCGTTT	89849
rs72969821	snp	A/C	0.0154538	0.0865337	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836438	CTCCCTCCTCAGCTG[A/C]CTCTATGCTATCTGC	89849
rs72969826	snp	C/T	0.0130921	0.0798413	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838284	CAGTCTGGGGACTAA[C/T]CTTGGGGAGGAGCCA	89849
rs73547762	snp	C/T	0.00540568	0.051707	intron-variant	ATG16L2	GRCh38.p7	11:72828784	GTGTTCAGGTATGTC[C/T]GTGAGAGCATATGCC	89849
rs74669541	snp	A/G	0.145642	0.227177	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837090	GAACTGCTCTATTTA[A/G]TAAGCATTTGAAGAT	89849
rs74697139	snp	C/T	0.00914312	0.0669923	intron-variant	ATG16L2	GRCh38.p7	11:72819615	ATTTCCTGCCACGCT[C/T]ATCTCTGAGCTCCCA	89849
rs74720753	snp	C/G	0.00636936	0.0560724	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823158	TTCCATCTCACCCCC[C/G]CAACCCCTACCCTCA	89849
rs75149850	snp	A/G	0.0111196	0.0737302	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828235	AGCCTTTACCCCAGC[A/G]ATCCAGGGCCCTGGG	89849
rs75185096	snp	G/T	0.0622301	0.165053	intron-variant	ATG16L2	GRCh38.p7	11:72816640	CATCTCTGGGCTCCT[G/T]CAGCCCTTTTAGCCG	89849
rs75362349	snp	C/T	0.0134861	0.0810011	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821084	CAGAACTCACATTCC[C/T]CTGACCAGCCTGGAG	89849
rs75429647	snp	C/T	0.040671	0.13668	intron-variant	ATG16L2	GRCh38.p7	11:72832802	ACTGGATTCAGATTC[C/T]GCAAAGGGGCTGGCC	89849
rs75528386	snp	A/C	0.00557542	0.0525036	intron-variant	ATG16L2	GRCh38.p7	11:72818925	GGACTCATTTGAGAA[A/C]CTTTCCCTAGAGCTG	89849
rs75772023	snp	A/C/G/T	0.0196033	0.0970431	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841600	TGCAGCAAAGGGAAG[A/C/G/T]GAGGTTACCCGGTGC	89849
rs75859052	snp	C/T	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72828858	TCTGACCCCCCGTTT[C/T]CTTGCTCTGCTGTGG	89849
rs75911233	snp	C/G	0.0298908	0.118541	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838731	GTGCCTAAAAAACAA[C/G]ACTGGCCAAACTCCA	89849
rs76079323	snp	A/G			missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841556	GCAGTGGAGGCAGGG[A/G]GGCGTGTGGCTTGGG	89849
rs76762469	snp	A/C	0.0528381	0.153711	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838329	CCCTCCTTCTGTTTC[A/C]TTATGTAGCCAACAT	89849
rs77392972	snp	G/T	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72819763	TTTCTTTTTTTTTTT[G/T]GAGACGGAGTCTCAC	89849
rs77419620	snp	C/G	0.0163588	0.0889482	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824802	AGATCATCCCTGTGT[C/G]TGTGGCTGCCCGACT	89849
rs77541177	snp	C/T	0.020127	0.0982772	intron-variant	ATG16L2	GRCh38.p7	11:72817736	GGGGGACATTGAGCA[C/T]CACTCTGATTGGTTG	89849
rs77663794	snp	A/G	0.0901694	0.192235	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840002	AAACGAGGCAAATGT[A/G]GAGAAGCACATCAGC	89849
rs77705768	snp	A/C	0.0123036	0.0774623	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838607	AGAAAATGACAACAA[A/C]AAAAAAAGGCACGAA	89849
rs77910635	snp	C/T	0.0119091	0.0762411	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837365	CATGGGGACATTTGG[C/T]GAGCATTTCAAGTTT	89849
rs77937957	snp	A/C	0.0498117	0.149749	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815361	TGCTCTTAGCCAGGA[A/C]AATTTCTCTGCAAGC	89849
rs78095359	snp	A/T	0.0166325	0.0896639	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823086	GAGGAGAGGCCAGAA[A/T]GCTCAGATCTCCCAG	89849
rs78238378	snp	C/T	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72830924	TGCATGCCACCGTGC[C/T]TGGCTATTTCCTTGC	89849
rs78333957	snp	A/T	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72833932	GTCTCAAAAAAAAAA[A/T]TTTTTTTTTTTTTCA	89849
rs78600286	snp	A/G	0.5	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837467	TTTCTTAACCAAGGA[A/G]AAAAAAAAAAAACAA	89849
rs79145554	snp	A/G			missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824122	TGAAGGGGCTTCTGG[A/G]GTAAGTGTGTGTGTG	89849
rs79332493	snp	A/G	0.0256215	0.110247	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815154	GCTGAGCCCAGCGAA[A/G]TCGGACTCTCAGAAT	89849
rs79343393	snp	A/T	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72833922	GCGAAACTCCGTCTC[A/T]AAAAAAAAAATTTTT	89849
rs79797230	snp	C/T	0.0160194	0.0880515	intron-variant	ATG16L2	GRCh38.p7	11:72825426	AGGAGCCCTCCCCTG[C/T]CGGCCAACTTGGTGC	89849
rs79961755	snp	A/G	0.0165278	0.0893908	intron-variant	ATG16L2	GRCh38.p7	11:72825701	GGTCCTACAGGGACA[A/G]GCCCTTGAAGAGCAG	89849
rs80099467	snp	G/T	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72819764	TTCTTTTTTTTTTTT[G/T]AGACGGAGTCTCACT	89849
rs111230135	snp	A/C	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72830467	CCAATCCTTTCCCTT[A/C]CTATGGCCAGAGTGA	89849
rs111271436	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72834896	AGCCATCATTCCATT[C/T]CTTTACAATTGAGGA	89849
rs111451981	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72817696	TGTAGCATCACTTGG[A/G]TGCCTTTGGGCACTT	89849
rs111478080	in-del	-/ATTC	0.0119091	0.0762411	intron-variant	ATG16L2	GRCh38.p7	11:72830788	CTTCATTTCCTTGCT[-/ATTC]TATTCATTCATTCAT	89849
rs111873688	snp	A/C	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72831506	GTGAAACTCCATCTC[A/C]ACAACAACAAAATTC	89849
rs111883118	snp	A/T	0.0126979	0.078662	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841011	GTTGTTGAGCAATAA[A/T]GCTGATGCAAGGCTG	89849
rs111948912	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836971	CTTCCAAAAAATATT[C/T]TAAAATACAACAAAA	89849
rs112124890	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814009	GCTGAGGGCCTCTGG[G/T]TCCCTGGCTGGGTGC	89849
rs112275640	in-del	-/T	0.5	0	intron-variant	ATG16L2	GRCh38.p7	11:72835748	TTATACTGGAACATA[-/T]TTTTTTTTTTTTTTT	89849
rs112613208	snp	A/C/T	0.0111196	0.0737302	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827038	TGGGTAGGAAAAAGA[A/C/T]GTGGGTGAGCCCTGT	89849
rs112951181	snp	A/C	0.0194124	0.0965887	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824038	CCAGTCCCTTAGCAT[A/C]TCTCTCTTGGTTTTG	89849
rs112981237	snp	A/G	0.0185938	0.0946107	intron-variant	ATG16L2	GRCh38.p7	11:72831584	CCAACATTCTTCGAT[A/G]CTCAGCCTTCTACTC	89849
rs113016055	snp	C/T	0.0433465	0.140692	intron-variant	ATG16L2	GRCh38.p7	11:72833214	AGCACATTTGCTGAA[C/T]TGAATAGAGGTGGTT	89849
rs113098516	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72834895	CAGCCATCATTCCAT[C/T]CCTTTACAATTGAGG	89849
rs113187035	snp	A/G	5.37139e-05	0.00518209	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829428	CTGGAGCTCTTGCCC[A/G]AAGCCTGAAGCTTCC	89849
rs113332022	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72834897	GCCATCATTCCATTC[C/T]TTTACAATTGAGGAT	89849
rs113430241	snp	A/G	0.5	0	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828360	TCCTTGTTCCTCAGG[A/G]GGCCCCACTGCACCC	89849
rs113447165	in-del	-/A	0.5	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838605	ATAGAAAATGACAAC[-/A]AAAAAAAAAGGCACG	89849
rs113500027	snp	A/G	0.0111196	0.0737302	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829648	GAACTGCGTCTGCCT[A/G]CCTCTTTGCAGCATT	89849
rs113984858	snp	C/G	0.0433465	0.140692	intron-variant	ATG16L2	GRCh38.p7	11:72832729	TGGGGCAGCTCCTTC[C/G]GGTCACAGAGCAGAG	89849
rs114002424	snp	A/G	0.0107246	0.0724382	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840592	TTTCACAATTAGCCC[A/G]CTTTAATGCTCATAA	89849
rs114158056	snp	A/G	0.0126979	0.078662	intron-variant	ATG16L2	GRCh38.p7	11:72830894	CTTAGCCTCCCCAGT[A/G]GCTGGGCCTATAGGT	89849
rs114646384	snp	A/C	0.0189856	0.0955633	intron-variant	ATG16L2	GRCh38.p7	11:72818558	AGGCTCACCATCTCC[A/C]CCAGAATTTGGCCCA	89849
rs114653296	snp	A/G	0.0228947	0.104514	intron-variant	ATG16L2	GRCh38.p7	11:72818850	GTGATAGCCCAGGAA[A/G]TACACATCCAGTCAC	89849
rs114835258	snp	G/T	0.00517822	0.0506191	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823429	CTTGTGGGACCTGAT[G/T]GGGGCTTCAGACCTT	89849
rs114876231	snp	A/G	0.0236746	0.106192	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839837	ATGGTTATCATAGCT[A/G]TGGAAGTAGATGAGG	89849
rs114942058	snp	A/G	0.00426843	0.0459999	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841540	GGCTGGTCGTACAAC[A/G]GCAGTGGAGGCAGGG	89849
rs115308215	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72818885	TGGCAAGTCACCTGC[C/G]CAACAGAAATGCGGG	89849
rs115313998	snp	C/T	0.0217236	0.101931	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836295	TCACACAATTCATTA[C/T]TCCTTAGGGTGGAGG	89849
rs115461335	snp	C/G	0.0232847	0.105357	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838171	AATACGAAGGACACT[C/G]TTATTTTAAGTCTGT	89849
rs115538122	snp	A/G	0.00517822	0.0506191	intron-variant	ATG16L2	GRCh38.p7	11:72818607	CTCCTTGCAGGCATC[A/G]GGCTAAACATTGTCT	89849
rs115701249	snp	A/G	0.00494653	0.0494853	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840999	CATTTTACTTGAGTT[A/G]TTGAGCAATAATGCT	89849
rs115859489	snp	G/T	0.021333	0.101051	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826413	TTTGCCTGCCTTGGT[G/T]ACCTGGGCCGTGGGA	89849
rs116210010	snp	A/G	0.0232847	0.105357	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841288	ATGAGCCGTGATCAT[A/G]CCACTGAACTCCAGC	89849
rs116243770	snp	C/T	0.021333	0.101051	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826422	CTTGGTGACCTGGGC[C/T]GTGGGAAACTGTGAG	89849
rs116530967	snp	A/C	0.02016	0.0983543	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813253	TCTACGTCCTCTGAC[A/C]CATCCCCATCAGAAT	89849
rs116591754	snp	A/G	0.0236746	0.106192	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840521	TTATTTCATCTTGGT[A/G]TTCCTCAAAGAGGCA	89849
rs116807477	snp	A/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72828587	GTAATAGACCCTCTT[A/G]GAGCCCTCCCTGGAG	89849
rs116884791	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839858	GTAGATGAGGTCATT[C/T]GGCAAGAGTGCGTTC	89849
rs116926964	snp	G/T	0.0182019	0.0936463	intron-variant	ATG16L2	GRCh38.p7	11:72833311	TACAGGCTCTTCCAC[G/T]GGAGACACATTCACT	89849
rs116970024	snp	C/G	0.0209421	0.100162	intron-variant	ATG16L2	GRCh38.p7	11:72825102	AGCATAGCACGGAGG[C/G]TGCTGCAGGGGTCCA	89849
rs117134203	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814027	CCTGGCTGGGTGCGC[A/G]GCCAGGAGCGCGACG	89849
rs117202859	snp	C/G	0.0165278	0.0893908	intron-variant	ATG16L2	GRCh38.p7	11:72825697	ATGAGGTCCTACAGG[C/G]ACAGGCCCTTGAAGA	89849
rs117283758	snp	A/G	0.00557542	0.0525036	intron-variant	ATG16L2	GRCh38.p7	11:72833415	GCTTGTTCCTACTTT[A/G]CAGATGAGGAAAGCA	89849
rs117512134	snp	A/G	0.0360663	0.129354	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838300	CTTGGGGAGGAGCCA[A/G]CCTCTCCTGAAATCC	89849
rs117558080	snp	C/T	0.00358779	0.0422022	intron-variant	ATG16L2	GRCh38.p7	11:72833629	TTTCAGCATAAAACA[C/T]TCTAGGAAAGGCCGG	89849
rs117778213	snp	A/C/T	0.00133609	0.0258123	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822459	CGCCAGGGTCTCAGG[A/C/T]TGCTTTTTACCCAAC	89849
rs118051917	snp	C/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836265	ATCCACCCCTGGGAC[C/T]GAGAAAATCTCCTTT	89849
rs118167348	snp	C/T	0.0182019	0.0936463	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823339	CGCAGGGACATGAGG[C/T]CACAGGTGTGTACAA	89849
rs137892262	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813791	CCGCACCCACCTGGC[A/G]TTTTCGTGTCACGGA	89849
rs138135570	snp	A/G	0.00953063	0.0683702	intron-variant	ATG16L2	GRCh38.p7	11:72828520	TCAGGTACCAGCCTC[A/G]TGCCTGCTGACCCTG	89849
rs138182296	snp	C/T	0.000101545	0.00712477	synonymous-codon, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829315	CAGCGCTGCCGTCAA[C/T]GCCGTGGCCTGGTGC	89849
rs138450793	snp	C/G	1.64876e-05	0.00287116	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816778	AAGTTCTCAAAGAAG[C/G]TGCAGCCGGAGCCAA	89849
rs138454321	snp	A/G	0.0372196	0.131242	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816182	GATGGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	89849
rs138528786	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821421	GGTTCCTAGTAGGGT[C/T]GCAGAGAAACGAAGC	89849
rs138669194	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839561	GCGAGCTCTCTGCAA[G/T]GTATACCTGGCAGGA	89849
rs138797856	snp	C/T	0.00676609	0.0577691	intron-variant	ATG16L2	GRCh38.p7	11:72832379	AGGTCCCCCTCCCAG[C/T]AGGAGGGGGTGCTTC	89849
rs138856854	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839004	AAATGTTGTGAGCAC[A/G]TGCTTTCAACCTAGT	89849
rs138910593	snp	A/T	1.64762e-05	0.00287016	stop-gained, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828953	GATGTGGACACCGGG[A/T]AACTGGAGAGCAGAC	89849
rs139161872	snp	C/T	8.4016e-05	0.00648081	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841539	AGGCTGGTCGTACAA[C/T]GGCAGTGGAGGCAGG	89849
rs139186024	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823169	CCCCCCAACCCCTAC[C/T]CTCAACCCTTTCCCT	89849
rs139239383	snp	A/G	0.000149577	0.00864675	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823797	CCAGGAACTTTTGTT[A/G]GTGGGTACTAGTAGG	89849
rs139269124	snp	C/T	0.00358779	0.0422022	intron-variant	ATG16L2	GRCh38.p7	11:72819211	CTGGAAATGCAGGGG[C/T]ACCTCTGACTCTTCC	89849
rs139269726	snp	C/G/T	6.58907e-05	0.00573948	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824083	CAGCCACCTCCCTGA[C/G/T]GCTGTCCCACTGTGT	89849
rs139388322	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824575	ACACCAACCCCTGGG[A/G]TCGAGGCTGGGTTGG	89849
rs139411354	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841073	TTTGGGATACTGAGG[C/T]GGGAGGATTACTTGA	89849
rs139549869	snp	A/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72829225	CCTCAAACTACCCAG[A/G]TCCAGCAGTCGGGGC	89849
rs139902397	in-del	-/CTGCCTC	0.146459	0.227551	intron-variant	ATG16L2	GRCh38.p7	11:72822580	TCCGACCCTTGCGTT[-/CTGCCTC]CCGCCCCGCCTGCCT	89849
rs139969359	snp	G/T	1.66308e-05	0.00288359	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840931	TGATGCCTGTGAGAA[G/T]CCTGGTGACTCAGCA	89849
rs140125425	snp	C/T	0.0023933	0.0345097	intron-variant	ATG16L2	GRCh38.p7	11:72825676	GATTGGTGGGGGTCC[C/T]CTATCATGAGGTCCT	89849
rs140147424	snp	C/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842427	AAGATGGAGGTGTGG[C/G]AGGATGGCCACATTC	89849
rs140264980	snp	A/G	0.0170251	0.090679	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836522	TCCCATGGGAAAAGC[A/G]AAGACCGTAACCTAT	89849
rs140291439	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812642	CCTTACCTGAGAGAA[A/G]CGGCATCTCTGCACC	89849
rs140378749	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840680	CAGTGAAAAAAGTTC[C/T]AGTGTAGATTAAATG	89849
rs140569553	snp	C/T	0.00398564	0.0444627	intron-variant	ATG16L2	GRCh38.p7	11:72831378	GGGCATGGTGGCACA[C/T]GCCTGTAATCCCAGC	89849
rs140791287	snp	A/G	0.0146672	0.084371	intron-variant	ATG16L2	GRCh38.p7	11:72818537	TTGGAGATCACATCT[A/G]AAATCAGGCTCACCA	89849
rs140836009	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815292	GAAGTCTAACCACAA[C/T]CCCTGCGGCTCTCTC	89849
rs140894436	snp	A/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72820474	AAAATATTGAATGGT[A/G]CAACACAACATAAAT	89849
rs141290464	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832980	GAGCTGTTCTGTAGG[C/T]ATGAGGACCATGGCC	89849
rs141309534	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838697	TTTTGCTCTGTTCAA[A/G]AGTCATCATCATGCA	89849
rs141447742	snp	C/T	0.00636936	0.0560724	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823410	GTGTAGATGTGTGCT[C/T]ACACTTGTGGGACCT	89849
rs141490660	snp	A/G	1.72187e-05	0.00293412	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822532	TGCCAAGCGGACCGT[A/G]AGCATCAGCGAGTAA	89849
rs141553336	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815924	TAATTGCTCAAGGAC[C/T]TTCTATTCTGGCCTG	89849
rs141855549	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828259	CCCTGGGGTTCCTCC[A/G]GACTTGGTTAGCTAG	89849
rs141914231	snp	A/G	2.15924e-05	0.00328569	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841549	TACAACGGCAGTGGA[A/G]GCAGGGAGGCGTGTG	89849
rs141976065	snp	C/T	0.000115393	0.00759493	missense, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828396	ATCCCTGTGCAGGGC[C/T]GGGTCACCTCCCTGA	89849
rs142195908	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72818800	CAATAAACAAGACCT[A/G]GCCCCATGGGGCTTC	89849
rs142241169	snp	C/T	0.000106061	0.00728145	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841458	AGAACCCTTACCGTT[C/T]GCTGAAGGAGACCGG	89849
rs142581537	snp	C/T	0.000148413	0.00861305	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826710	GGGTACAGGAGACAC[C/T]GTCTGGACACAAGGA	89849
rs142624444	snp	C/T	0.000181376	0.0095213	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843194	AACGAGTTCTGCTTC[C/T]GTGGAATTGCTGGAC	89849
rs142632291	snp	A/C	0.00664166	0.0572448	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826693	ATCCGTACCTGGGGC[A/C]GGGGTACAGGAGACA	89849
rs142644434	snp	A/C	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72830889	CCTGCCTTAGCCTCC[A/C]CAGTAGCTGGGCCTA	89849
rs142677944	snp	A/G	0.00398564	0.0444627	intron-variant	ATG16L2	GRCh38.p7	11:72832405	GCTTCCTGGAGGAAC[A/G]AGTCTGTAAGGCCAG	89849
rs142724039	snp	C/T	0.000141794	0.00841883	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840843	AATTTGGAAGAACTA[C/T]GCATTCGATAATCCT	89849
rs142770133	snp	A/G	0.000252332	0.0112295	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829337	GCCTGGTGCTACTCC[A/G]GGAGCCACATGGTGA	89849
rs142927800	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837771	AAATGTCAGGGTAGT[A/G]GGACCTGGAAGCTGC	89849
rs143025776	snp	C/T	0.0494327	0.149241	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815559	GAGGGACTAGAGAGA[C/T]CTGGAGGGCTGAAAT	89849
rs143300353	snp	A/C/T	0.000232511	0.0107801	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814491	GCAGCGCGCTGGAAA[A/C/T]GCCACATCGTGCGGC	89849
rs143377298	snp	C/T	0.000629076	0.0177245	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825332	GAGGTCAATGCTGTT[C/T]GTTTTGGCCCCAACA	89849
rs143543601	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840467	AATAATATATTCACC[C/T]GGAGAATAAACGCTC	89849
rs143553457	snp	A/C	0.00755907	0.0610114	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840119	CCTATATCCTTTCTG[A/C]CACCCTCCATCCATC	89849
rs143798722	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821246	GAGGATGGAAGGAGC[C/G]TGTAGCCTGCTGGGA	89849
rs143921286	snp	A/G	0.00358779	0.0422022	intron-variant	ATG16L2	GRCh38.p7	11:72817509	CAGGTGTGAGCCACC[A/G]CGCCTGACTGGGAGG	89849
rs144001366	in-del	-/C	0.0235167	0.105855	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836507	GTATTTCTTTTTTTT[-/C]CCCATGGGAAAAGCA	89849
rs144002516	snp	C/T	1.64944e-05	0.00287175	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816809	ACAGTGTCACTCCCA[C/T]CACCCACCAGGGCCC	89849
rs144019051	snp	A/C/G	0.00937818	0.0678459	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822381	TGTCTGGAAGGGAGG[A/C/G]GGGCAGCAGCCGCCC	89849
rs144118330	snp	G/T	0.000399281	0.0141238	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824762	AGAGGTCACTCAATT[G/T]GGGGAGCCCCTGAGC	89849
rs144200516	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842680	AAAGTTCTTCCACTA[A/G]CACCGATGGGAAAAC	89849
rs144262601	snp	A/G	1.69026e-05	0.00290706	splice-acceptor-variant	ATG16L2	GRCh38.p7	11:72817755	TCTGATTGGTTGGCA[A/G]GGAGGAGTCAGAGCT	89849
rs144487404	in-del	-/TCTA	0.497271	0.0368399	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829587	CTTTGTATTTTTATC[-/TCTA]CTCTATCTCCTCACT	89849
rs144675215	snp	C/G	0.00993419	0.0697739	intron-variant	ATG16L2	GRCh38.p7	11:72818668	GAGGAGGAAACTGAG[C/G]CTTGGAGAGGTAGAG	89849
rs144745719	snp	C/T	0.000102615	0.00716219	synonymous-codon, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829303	CCTCCCTTTCCCCAG[C/T]GCTGCCGTCAACGCC	89849
rs144900518	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72830919	ATAGGTGCATGCCAC[C/T]GTGCCTGGCTATTTC	89849
rs144952535	snp	A/G	0.000153988	0.00877327	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841544	GGTCGTACAACGGCA[A/G]TGGAGGCAGGGAGGC	89849
rs145036173	snp	C/G	0.00239393	0.0345281	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839003	GAAATGTTGTGAGCA[C/G]GTGCTTTCAACCTAG	89849
rs145073390	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830584	AAGCAATCCTCCCAC[C/G]TGGTCTTCCCGAAGG	89849
rs145084668	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72835182	CGGAACCTCCAGTAC[C/G]GAAAGCAGCTTTCAC	89849
rs145319072	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812925	CAGAGACATCTAGGA[A/C]CCAGGTCCTGCCCTA	89849
rs145360918	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842151	GTGATGAACTAAGTC[G/T]AGGGTCACTTGAGTG	89849
rs145435818	snp	A/C	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820822	TGGGGTCTGTCTCTC[A/C]CACCGACCCTGCTTG	89849
rs145635734	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839414	AGGTAACAACTGGAG[A/G]AAGGATCAGAGGCAA	89849
rs145880755	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837568	ACAGTCAGCACCTGA[C/T]GTGGGGGCACCTGCT	89849
rs146005831	snp	C/T	0.000378872	0.0137584	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828949	CTGGGATGTGGACAC[C/T]GGGAAACTGGAGAGC	89849
rs146015778	snp	G/T	8.31663e-05	0.00644796	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840888	TTACAGGTCGCAGTT[G/T]GCCATATGAGGTCTC	89849
rs146039885	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832627	TTTCAGAACTCTGGT[A/G]CTCAGGGGCTGCCTG	89849
rs146056807	snp	A/G	0.00438332	0.0466095	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828282	TTAGCTAGGAAGGCT[A/G]CTGCGCCTGGCCCCT	89849
rs146470112	snp	C/T	0.00398564	0.0444627	intron-variant	ATG16L2	GRCh38.p7	11:72820018	CCAAAGTGCTGGGAT[C/T]ACAGGCGTGAGCCAC	89849
rs146474296	snp	C/T	0.00526955	0.0510589	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824840	CGGGCTCAGGATGTG[C/T]TGGTAAGGGAGGAGC	89849
rs146520723	snp	C/T	0.000159471	0.00892806	missense, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824825	GCCCGACTTCCTACC[C/T]GGGCTCAGGATGTGC	89849
rs146786729	snp	A/G	0.000155563	0.00881802	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826840	TGAGCCCGAGCCCCA[A/G]CCCCACCTCTCCTCC	89849
rs147103732	snp	A/G	0.00016484	0.00907704	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828461	TTCCCGAGACAACAC[A/G]CTCAAGGTCATCGAC	89849
rs147121349	snp	G/T	7.03953e-05	0.00593234	utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814529	GCTTCGGGACCGTAC[G/T]CAAAAGGCGCTTTTC	89849
rs147280877	snp	A/G	0.00597247	0.0543191	intron-variant	ATG16L2	GRCh38.p7	11:72817983	TGAGTGAGCCCTAGT[A/G]TGTGCCAGGCCCTGA	89849
rs147756960	snp	G/T	0.00358779	0.0422022	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826307	CACACTGGGCAGGTG[G/T]GGGCTGTGGGACCTG	89849
rs147782509	snp	A/C/T	6.5893e-05	0.0057396	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842703	GGGAAAACTCCAATA[A/C/T]GCCCATTGAATTCCC	89849
rs148027442	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840358	AAATTGCAAAGTATC[C/T]GACTGGATTACCGTG	89849
rs148109459	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828172	CTGTCTAAGTTCCTC[A/G]ATGGAGGCAGCTGGC	89849
rs148261464	snp	C/G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825145	AACACCTGGTGGGGC[C/G/T]GGGTTTGAAACTCAG	89849
rs148266386	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832728	ATGGGGCAGCTCCTT[C/T]GGGTCACAGAGCAGA	89849
rs148387255	snp	G/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815781	TGGGAAGGAAGTTGA[G/T]GAGGAGGGAGCTAGG	89849
rs148427877	snp	C/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72830062	ACTGGGTCCGCGTTC[C/T]TCCTCCAGGGGTAGT	89849
rs148638811	snp	A/C/G	5.08689e-05	0.00504304	intron-variant	ATG16L2	GRCh38.p7	11:72825251	GCCCGTGAGCACTCA[A/C/G]AGAGACATGCGCGGG	89849
rs148693633	snp	A/C	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72818793	AGTGCAACAATAAAC[A/C]AGACCTGGCCCCATG	89849
rs148743255	snp	C/T	0.000153988	0.00877327	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822524	AAGAAGGCTGCCAAG[C/T]GGACCGTGAGCATCA	89849
rs149006588	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837760	TCCTTCCACGGAAAT[A/G]TCAGGGTAGTGGGAC	89849
rs149012164	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820924	GCCAGCGCTGTTCCC[A/G]TATTGAGTCTGGGCC	89849
rs149313870	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839789	GAAGAGATCGGATTG[G/T]CAGTTATAAATCTGA	89849
rs149363742	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72818621	CGGGCTAAACATTGT[C/T]TCAGTTAATCCTTCA	89849
rs149372160	snp	A/G	0.000153988	0.00877327	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828967	GAAACTGGAGAGCAG[A/G]CTACAGGGACCCCAT	89849
rs149383628	snp	A/G	0.00795532	0.062565	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827444	CAGCTAGTGCCTCTC[A/G]GCTGGGCTCAGCTCC	89849
rs149714414	snp	A/G	0.00105006	0.0228895	intron-variant	ATG16L2	GRCh38.p7	11:72829258	AGCCAGGTTGCAGGC[A/G]CAGTTCCTGAAGCCC	89849
rs150089868	snp	A/G			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820636	ACTCACTCACATAGC[A/G]CGTCATGTCAGTGCA	89849
rs150243335	snp	A/G	3.29522e-05	0.00405894	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828950	TGGGATGTGGACACC[A/G]GGAAACTGGAGAGCA	89849
rs150767189	snp	C/T	0.000206872	0.0101683	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841499	GGGAGCTCCTCTTAT[C/T]TGGGCTGGGGTAGGG	89849
rs150768612	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72833146	TGAGTGTCTCCCACC[A/G]GATGCAAGCCCCTCA	89849
rs150821280	snp	A/G	0.000154655	0.00879225	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822883	ATGGGATGAGGGAGA[A/G]AAGGGAGACTCTGGC	89849
rs150850600	in-del	-/GGAGGAAGGGA	0.0179601	0.0930455	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822400	CAGCAGCCGCCCCCT[-/GGAGGAAGGGA]CCGGGTCTAGCCCCG	89849
rs151076964	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838634	CGAAATATTCAAAAC[A/G]TGGGAGGAGTCTACC	89849
rs151146589	snp	A/C/G	0.00159649	0.0282165	intron-variant	ATG16L2	GRCh38.p7	11:72825557	AATGCCTTGGAAAGA[A/C/G]TGAGACTCTGGGCTC	89849
rs180690361	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72826100	GGAACTGATCTTCCG[C/T]TCTCAATCCCAATTC	89849
rs180837744	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840817	CGGGGAAACATTAAT[C/T]CCTTACTTTCAATTT	89849
rs180875949	snp	A/C/G	0.000511351	0.0159824	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816815	TCACTCCCACCACCC[A/C/G]CCAGGGCCCCTGGTA	89849
rs180881361	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836799	TAAATACAAACTTTT[C/T]ACAGCCACTGTAAAG	89849
rs180970395	snp	A/G	0.00199481	0.0315187	intron-variant	ATG16L2	GRCh38.p7	11:72832748	CACAGAGCAGAGCTG[A/G]GATAAGAACCCAGAC	89849
rs181010657	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821422	GTTCCTAGTAGGGTC[C/G]CAGAGAAACGAAGCG	89849
rs181241692	snp	C/T	0.00873819	0.065519	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822038	TCCGCTCTTTCCGTC[C/T]TCCAGGCTGGCAGCC	89849
rs181484325	snp	C/T	0.00358779	0.0422022	intron-variant	ATG16L2	GRCh38.p7	11:72832071	AGCCTGGACGGTTAG[C/T]ATCCCTTGAAGTGAG	89849
rs181588123	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72832288	ACTTTATGGGCGTCA[A/G]TCTTACCACACACGC	89849
rs181866073	snp	C/T	8.71376e-05	0.00660009	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826814	GAGTGGGACCTCGGC[C/T]GTGCCTATTGTGAGC	89849
rs181881012	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823256	CAGGAGAGAACCTGT[A/G]GGCAAAGCCCAGAGC	89849
rs181961231	snp	A/G	0.000165645	0.00909918	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838819	ATTTCCACATCTTCA[A/G]TCTTCTCTGCTGGCC	89849
rs181988926	snp	A/C	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815955	GGGGTACCTTACACC[A/C]GGGCTGGGGAAGTTG	89849
rs182262565	snp	C/T	1.65121e-05	0.00287329	intron-variant	ATG16L2	GRCh38.p7	11:72828521	CAGGTACCAGCCTCA[C/T]GCCTGCTGACCCTGT	89849
rs182449947	snp	A/G	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827485	TGTGCCACTGTCTTC[A/G]TGGCTCTTGGTCCAA	89849
rs182685271	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823405	AGCATGTGTAGATGT[A/G]TGCTCACACTTGTGG	89849
rs182686987	snp	G/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824218	ACCTGTCCATCCCTG[G/T]GATGTGCAGCTGTCT	89849
rs182821787	snp	A/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819616	TTTCCTGCCACGCTC[A/T]TCTCTGAGCTCCCAG	89849
rs182847493	snp	C/G/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829639	ATGATATCTGAACTG[C/G/T]GTCTGCCTACCTCTT	89849
rs182853389	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812643	CTTACCTGAGAGAAA[C/T]GGCATCTCTGCACCT	89849
rs182863360	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834927	TGTGGCAGCTAAGAG[A/G]GAAAGGTCTTCCATC	89849
rs182976224	snp	A/C	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817433	ACCATGTTGGCCAGG[A/C]TGGTCTCGATCTCTT	89849
rs182991888	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842452	ACATTCCACAAGGGA[C/T]TGACTGACAAGTCTC	89849
rs183015860	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72830503	GTTGTTGTTGTTGTT[G/T]CTTTTGAGACACACA	89849
rs183147361	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72836040	GGCATGAGCCACTGC[A/G]CCCGGCTGAACACAT	89849
rs183148632	snp	C/T	0.00953873	0.0683987	intron-variant	ATG16L2	GRCh38.p7	11:72832252	CAGTGAGCCCTTCTC[C/T]CCCCCAAAACCTTCC	89849
rs183300933	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72834320	ACCAAAAGCTGCAGC[G/T]GGGTTCTTCAGGCAG	89849
rs183582088	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831161	TAGATTATTTCCTGG[A/G]ATCAGGCCTGGCACA	89849
rs183795968	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815427	AGGCCAGCCCCCACC[C/T]CCAGCAGCCACACTT	89849
rs183930380	snp	C/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813465	GAGCTGGCTCTCTAG[C/T]ATCTAGCTAGAGACG	89849
rs183931234	snp	A/G	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72818441	GGTTCACTGACCCCC[A/G]TTTTTTCTGTTTGCC	89849
rs184051572	snp	A/C/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72820384	TTCACCCCTCTCCCC[A/C/G]CAACCATCCCTAACC	89849
rs184051998	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72816984	TGGGGGTGGTGGGGG[A/G]GGCAGGCCCTTGGCC	89849
rs184167046	snp	A/C			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826260	TGAGGAACTCTGCCC[A/C]AGTGGCATGGGATTG	89849
rs184449954	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838272	GTTTCACTTTCTCAG[C/T]CTGGGGACTAACCTT	89849
rs184479860	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814952	GAAAGAACGCGGGAC[A/T]TGTCCAGAGCAGCCA	89849
rs184563491	snp	A/G	0.000202703	0.0100653	intron-variant	ATG16L2	GRCh38.p7	11:72825264	CACAGAGACATGCGC[A/G]GGGAGGGCCGGGGCA	89849
rs184616354	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832233	GTCTGACTGATCTCT[A/G]GGACAGTGAGCCCTT	89849
rs184712120	snp	C/T	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72830398	CTGCTGGTTCTAGTA[C/T]TCCTCCACCCTCCTG	89849
rs184793041	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814403	CCCGGCCTGGCGCCG[A/T]CCTGGGCGGGAGGAA	89849
rs184863000	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72835749	TATACTGGAACATAT[A/T]TTTTTTTTTTTTTTT	89849
rs184900038	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837690	TGTGCAGGGTGCGCA[A/G]TCCTTCAGTCCTTTC	89849
rs184985774	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821579	GGGGCGGGCAGGTGA[A/G]CAGCCGACTCCCTTA	89849
rs185219028	snp	A/G	0.00265705	0.0363519	intron-variant, missense	ATG16L2	GRCh38.p7	11:72824727	ACCCCAACCCACCTT[A/G]CCCCAGTTTTAAGAA	89849
rs185295626	snp	C/G/T	3.43161e-05	0.00414211	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822471	AGGATGCTTTTTACC[C/G/T]AACAAGGGCCAAGCA	89849
rs185739122	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821171	GCAAGACACTTAAAC[C/T]TCTCTGTCGGTGTCC	89849
rs185907791	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837460	AATTTGATTTCTTAA[A/C]CAAGGAAAAAAAAAA	89849
rs185941148	snp	A/G	0.00478085	0.0486577	intron-variant	ATG16L2	GRCh38.p7	11:72817954	GAATTCTCCAAGCCC[A/G]GTGCTGCAAGCATTG	89849
rs185960628	snp	A/T	0.00716266	0.059414	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842466	ACTGACTGACAAGTC[A/T]CTGGTTTCCCAAATG	89849
rs186156587	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834505	TGTGACCTTTTTTGT[A/G]TGATGTTCTCTGTAT	89849
rs186162233	snp	A/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72833432	AGATGAGGAAAGCAG[A/G]GTCCAGAAGGTGAAG	89849
rs186305267	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828138	AAGGTTTCAAAGGCT[C/T]CAGCTTTCAAATCAA	89849
rs186509225	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817100	CCACCCCTATACTTA[C/T]GTCTTTTCCCTTTCT	89849
rs186563184	snp	C/T	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72832301	CAATCTTACCACACA[C/T]GCTGCTGCCATCGGG	89849
rs186734312	snp	A/C/G	0.00057876	0.0170032	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840850	AAGAACTATGCATTC[A/C/G]ATAATCCTGCAAGAT	89849
rs186814271	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72830804	ATTCATTCATTCATT[C/T]ACTCATTTAGAGATG	89849
rs186882145	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826958	AAACCTCTCAAGGCC[C/T]TCCAATTCCCTAATG	89849
rs187003149	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839650	AGTAGGATGGGGGTT[C/G]CATTTACCAAGATAG	89849
rs187142195	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824247	CTGCCTGTGAGTCTG[C/T]TGGGCCTTGGAGACA	89849
rs187219589	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72816252	CCCAGAGCGCTGGGA[A/G]TTCAGGTGTGAGCCA	89849
rs187294169	snp	A/G	3.32011e-05	0.00407424	intron-variant	ATG16L2	GRCh38.p7	11:72828556	TTTGCTGGGACAGCT[A/G]AGCCTCTCTTCTCCT	89849
rs187305817	snp	C/T	0.00279162	0.0372561	intron-variant	ATG16L2	GRCh38.p7	11:72819643	CCAGCTCCCTTTGCC[C/T]GAGATACTTTCCCTG	89849
rs187389025	snp	C/T	0.00279162	0.0372561	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823296	CCAGGCATGTGTGCG[C/T]AGCCATAGGTGTGCA	89849
rs187637973	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813689	GGCTTTCTAGATGAA[A/G]TCAGCTGCACCCCTT	89849
rs187755588	snp	A/C	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72830569	TAAACCCCTGGGTTT[A/C]AGCAATCCTCCCACC	89849
rs187882198	snp	C/G	0.00318978	0.0398085	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812971	ATTACAGGATGGTGT[C/G]ATAACTGGTGACGGT	89849
rs187904831	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835494	CACACTTTATATGGC[C/T]TTCCTGGAACCACAG	89849
rs187929629	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72836132	AATGCTTACTGCATG[C/T]CCCCAGCTCCAGGAA	89849
rs188033427	snp	C/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821937	GGCTTAGCCACCCGG[C/G]TAGCCGCGTTTGGCA	89849
rs188182920	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825528	CTGGAATATTCTGTG[A/G]GCAGTGACTAGACAA	89849
rs188671842	snp	A/C	0.0159072	0.0877528	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814439	CGCTAGGCGGGAGAG[A/C]GCGGCCATGGCGGGG	89849
rs188714442	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829860	ACTCTTGGTCCAACC[C/T]GGTCCTGAGGCCAAA	89849
rs188848404	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72817627	TTCCTTTACTGGCTT[G/T]CTGGCTTCCATCTTC	89849
rs188879480	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825031	GATGTGGGCATAAGC[C/T]GGGGAGGGAGAGAGA	89849
rs188882423	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819050	GCCCTGGGATGTCTT[C/T]GTTTGCCTCCGAGGC	89849
rs188958650	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838772	TGATTGTAGCAGTAA[C/T]GGATGGGCAAGCCCA	89849
rs189135984	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820810	AGCTGCCTTGCCTGG[A/G]GTCTGTCTCTCCCAC	89849
rs189185936	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816449	CTCAGGACCCTCAGC[A/G]GGCAGTACCCCGCAG	89849
rs189210868	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838038	TCAGATCCGGAAGTT[A/C]CATTTCTGCTTTAGC	89849
rs189398803	snp	C/T	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72832517	ATGTCAGCGGGAAGG[C/T]TGTTCCTCCCTCCAG	89849
rs189462062	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840332	AAAGCTAATAGGGGT[C/T]AAGGAAAATAAAATT	89849
rs189529446	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837729	AGCTGGTTTCCTCCA[C/T]GAGCCACCAGGTTCT	89849
rs189577095	snp	C/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815943	TATTCTGGCCTGGGG[C/G]TACCTTACACCAGGG	89849
rs189714001	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831580	GGCTCCAACATTCTT[C/T]GATACTCAGCCTTCT	89849
rs189715605	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823712	GTGAGCCTAGGCTCC[C/T]CCCTCCTCCCATCCC	89849
rs189768107	snp	C/G	0.0128334	0.0790756	intron-variant	ATG16L2	GRCh38.p7	11:72828854	CCCCTCTGACCCCCC[C/G]TTTTCTTGCTCTGCT	89849
rs189813896	snp	A/C/G	0.000831902	0.0203796	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826481	AAGAATGTTGCCTCC[A/C/G]GCTTAGCACCTCTCA	89849
rs190030912	snp	C/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828267	TTCCTCCGGACTTGG[C/T]TAGCTAGGAAGGCTG	89849
rs190036902	snp	A/G	0.0103295	0.0711199	intron-variant	ATG16L2	GRCh38.p7	11:72817363	GCCTCAGCCTCCTGG[A/G]ACGTGCACCACCACC	89849
rs190050244	snp	A/T	0.000433695	0.0147194	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840937	CTGTGAGAATCCTGG[A/T]GACTCAGCATGAAGG	89849
rs190354024	snp	A/G	0.00199481	0.0315187	intron-variant	ATG16L2	GRCh38.p7	11:72818048	AGCCCAGGATGAAGT[A/G]GGCTCCAACAGCAGC	89849
rs190366587	snp	A/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842969	AGTTGTAATTTTTTT[A/T]CTCACTGATGAATGA	89849
rs190522629	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823153	GTCAGTTCCATCTCA[C/T]CCCCCCAACCCCTAC	89849
rs190592433	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821321	CGCGAGGAGTCCTCG[A/C]AGTGGTTATGCATGG	89849
rs190635340	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834235	TGAACAAAATAAATG[C/T]GAAGATTCAGAGCAG	89849
rs191454413	snp	G/T	0.00279162	0.0372561	intron-variant	ATG16L2	GRCh38.p7	11:72830822	TCATTTAGAGATGAT[G/T]TCTCACTATGTTGCC	89849
rs191474724	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827064	CCTGTGCTGGGAAGC[A/G]GAAGACCTGGGTTCT	89849
rs191623327	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829587	TCTTTGTATTTTTAT[A/C]TCTATCTCCTCACTT	89849
rs192083168	snp	C/G	0.00279162	0.0372561	intron-variant	ATG16L2	GRCh38.p7	11:72834665	TTGGCTCACCGCAAC[C/G]TCTGCCTCCTGGGTT	89849
rs192234097	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823315	CATAGGTGTGCAAGC[A/G]TGTGCATCCGCAGGG	89849
rs192265025	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835028	GGTGGGTCAGAGAGG[A/G]AGGGGATCTAGGTGG	89849
rs192289484	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838207	GTGGAAGAGATGTGC[A/G]TTAATGCAATTGGTG	89849
rs192290007	snp	A/C			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815424	GCGAGGCCAGCCCCC[A/C]CCTCCAGCAGCCACA	89849
rs192323223	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814634	CGGGGAGAGGGTTTG[A/G]CTGGCTCCTCCGCCT	89849
rs192398642	snp	A/C			intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842881	CTGGTAAGATAATTA[A/C]CAGCCGGTTGCTTTT	89849
rs192402186	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813239	GGCCTTCACTGCTTT[C/T]TACGTCCTCTGACCC	89849
rs192417812	snp	A/G	0.00358779	0.0422022	intron-variant	ATG16L2	GRCh38.p7	11:72835928	CAATTTTGTATTTTC[A/G]GTAGAGACTGGGTTT	89849
rs192517947	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819325	TCTGACATAGTACAA[A/G]TAACTTTCATCCTGC	89849
rs192569446	snp	A/G	0.0252325	0.109451	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814037	TGCGCGGCCAGGAGC[A/G]CGACGGCCTGGGAAG	89849
rs192817013	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829890	AGCAACATGTTGGGC[C/T]CACCTGCTTCAGGCA	89849
rs192828644	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72833946	AATTTTTTTTTTTTT[C/T]AGGAAAATATTCCCA	89849
rs192980887	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824354	CATCCAAGGTCGTCA[C/G]AGGGGACCAAGAGCT	89849
rs193016268	snp	A/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820849	CTTGGCTCTGGGTTG[A/C]AGGCATGACGAGTGA	89849
rs193273361	snp	C/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72825192	CTGGGGAGGGAGATA[C/G]CACGTCTGCAGCAGG	89849
rs199542942	snp	A/G	6.59957e-05	0.005744	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826543	TTTTAGCAGCAACTT[A/G]CAACCAGGCTGCCCA	89849
rs199579390	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822984	CCCAGGTGACAGTCT[C/T]AGAGCTCTGAGCTGA	89849
rs199588445	snp	C/G/T	0.000476186	0.0154231	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826480	GAAGAATGTTGCCTC[C/G/T]GGCTTAGCACCTCTC	89849
rs199623106	snp	A/G	2.11584e-05	0.0032525	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841462	CCCTTACCGTTTGCT[A/G]AAGGAGACCGGGGAA	89849
rs199726953	snp	C/T	0.000397891	0.0140992	missense, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824760	GGAGAGGTCACTCAA[C/T]TGGGGGAGCCCCTGA	89849
rs199851515	snp	A/G	0.000230608	0.0107355	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828915	CACTGGCAGGCTCCT[A/G]TGATGGGGCCCTTTA	89849
rs199977799	snp	C/G	6.61452e-05	0.0057505	intron-variant	ATG16L2	GRCh38.p7	11:72828698	GACTAGTGATGACCT[C/G]TGTTCTGACCCCAGC	89849
rs199982763	snp	A/G	0.000461232	0.015179	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824155	TGTGTGTGCACCCAC[A/G]TGTGTGTCGGGCTCC	89849
rs200023715	snp	A/G	0.000399281	0.0141238	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843195	ACGAGTTCTGCTTCC[A/G]TGGAATTGCTGGACG	89849
rs200042497	snp	A/G	0.00166456	0.0288012	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826608	AGGCCTGACTGGGGA[A/G]GCTGCCTGGAGGTCA	89849
rs200044683	snp	C/G/T	0.000118444	0.00769484	intron-variant	ATG16L2	GRCh38.p7	11:72825263	TCACAGAGACATGCG[C/G/T]GGGGAGGGCCGGGGC	89849
rs200046023	snp	C/T	0.0014944	0.0272941	intron-variant	ATG16L2	GRCh38.p7	11:72816867	ACAAAGGGCTGCCTG[C/T]GCTGGGGCCCTGCCC	89849
rs200160307	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828286	CTAGGAAGGCTGCTG[A/C]GCCTGGCCCCTTCCT	89849
rs200280731	in-del	-/TCTGCC			intron-variant	ATG16L2	GRCh38.p7	11:72822579	GTCCGACCCTTGCGT[-/TCTGCC]TCCCGCCCCGCCTGC	89849
rs200337344	snp	A/C	2.44807e-05	0.00349854	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838842	TGCTGGCCTTCGGTG[A/C]TTCTGTGTAGGTGGA	89849
rs200377316	snp	C/T	0.00299557	0.0385851	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842777	ACGGATTATTGCTCC[C/T]TCAGGAAAAGATAAC	89849
rs200391084	snp	C/T	0.000115318	0.00759249	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842750	ATCATCTTGGTTTTC[C/T]TTGTTCAAGATACGG	89849
rs200423702	snp	G/T	0.000145028	0.00851428	intron-variant	ATG16L2	GRCh38.p7	11:72826129	TCCTCCATTTTGTGA[G/T]GTTAAGACCTCATTT	89849
rs200456427	snp	C/T	0.000399281	0.0141238	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822489	CAAGGGCCAAGCAGG[C/T]GCGGGTGTCCCAGGA	89849
rs200478307	in-del	-/GAG	0.0150606	0.0854603	intron-variant	ATG16L2	GRCh38.p7	11:72833221	TTGCTGAATTGAATA[-/GAG]GTGGTTTCTGGAGAG	89849
rs200672561	snp	C/G	4.96159e-05	0.00498051	intron-variant	ATG16L2	GRCh38.p7	11:72828538	CCTGCTGACCCTGTG[C/G]CCTTTGCTGGGACAG	89849
rs200684861	snp	C/T	0.00178316	0.0298061	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843114	ACAGTTTAGGTCAAA[C/T]GTGACCAAATAAAGA	89849
rs200687115	snp	C/T	0.00028187	0.0118683	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840916	CTCAGGAGTATGCCT[C/T]GATGCCTGTGAGAAT	89849
rs200728373	snp	A/G	0.000198026	0.00994857	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816818	CTCCCACCACCCACC[A/G]GGGCCCCTGGTAAGT	89849
rs200746293	snp	A/G	0.00363119	0.0424548	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817821	GGGTGAAGTGGCAGG[A/G]GGAGGAGGAGGGGCT	89849
rs200783836	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837813	TAGCAGTTGGTCTGG[A/C]CCAGCCACAGCCTGG	89849
rs200822228	snp	A/G	1.64738e-05	0.00286995	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824129	GCTTCTGGAGTAAGT[A/G]TGTGTGTGCCTGTGT	89849
rs200865441	snp	C/T	1.68315e-05	0.00290094	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829335	TGGCCTGGTGCTACT[C/T]CGGGAGCCACATGGT	89849
rs200934612	snp	A/C/G	0.000135575	0.00823219	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822034	GCTATCCGCTCTTTC[A/C/G]GTCCTCCAGGCTGGC	89849
rs201100842	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72817314	GATCTCAGCTCACTG[C/G]AACCTCTGCCTCCTG	89849
rs201145516	in-del	-/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841383	ATGCAGTTTTTTTTT[-/T]GCCCTTCAGGCGAAT	89849
rs201194597	snp	C/T	0.0086084	0.0650392	intron-variant	ATG16L2	GRCh38.p7	11:72816845	AAGTGTATGTGGGTC[C/T]GTGGTCACAAAGGGC	89849
rs201269620	snp	A/G	0.000341785	0.0130681	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841455	AGGAGAACCCTTACC[A/G]TTTGCTGAAGGAGAC	89849
rs201308008	snp	C/T	0.000115393	0.00759493	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827277	AATGACCAGAAGATC[C/T]GGTTCTGGGACAGCA	89849
rs201419985	snp	A/C/T	0.000105771	0.00727161	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822430	GTCTAGCCCCGCCTG[A/C/T]GTGCGAGGCGCCGCG	89849
rs201429666	snp	A/G	9.94102e-05	0.00704948	missense, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825324	ACCTCTCTGAGGTCA[A/G]TGCTGTTCGTTTTGG	89849
rs201449569	snp	A/G	8.24722e-05	0.006421	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826609	GGCCTGACTGGGGAG[A/G]CTGCCTGGAGGTCAG	89849
rs201600699	snp	A/G	1.67198e-05	0.0028913	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824775	TTGGGGGAGCCCCTG[A/G]GCAGCGATACCAGAT	89849
rs201613221	snp	A/G	0.000321982	0.0126841	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842846	CACAAAACATACTAG[A/G]GAGCAAGAGAAAAAC	89849
rs201617758	snp	C/T	8.3273e-05	0.0064521	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826505	CCTCTCACTTCCTCT[C/T]CCATTTCTCCAGGGC	89849
rs201682261	snp	C/T	1.65803e-05	0.00287922	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840911	GAGGTCTCAGGAGTA[C/T]GCCTTGATGCCTGTG	89849
rs201700689	snp	A/G	0.000399281	0.0141238	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72821689	TACCAGGTGGTGGAG[A/G]AGGGCGCGGCCCTGG	89849
rs201702623	in-del	-/AGGAGAGGTGGTGGTG			intron-variant	ATG16L2	GRCh38.p7	11:72835403	GTGGTGAGAAAAGGC[-/AGGAGAGGTGGTGGTG]AGGAGAGGTGGTGGT	89849
rs201827763	snp	C/G/T	3.2948e-05	0.00405871	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824034	CCAGCCAGTCCCTTA[C/G/T]CATATCTCTCTTGGT	89849
rs201873625	in-del	-/TTTT	0.0103295	0.0711199	intron-variant	ATG16L2	GRCh38.p7	11:72830258	ACGGTGTTGGTTAAA[-/TTTT]TGGCAACACCTACAC	89849
rs201930699	snp	C/T	3.29745e-05	0.00406031	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816785	CAAAGAAGCTGCAGC[C/T]GGAGCCAAACAGTGT	89849
rs201938834	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72830509	GTTGTTGTTGCTTTT[A/C]AGACACACAAAAAAC	89849
rs201982526	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72826082	GTGTCGGGGGGTGGG[A/G]CGGGAACTGATCTTC	89849
rs202152915	snp	A/G	1.64746e-05	0.00287002	intron-variant	ATG16L2	GRCh38.p7	11:72828813	CCTGTGTCCAAGTGT[A/G]CCCTGCCGGACCCTG	89849
rs202165878	snp	C/T	1.66405e-05	0.00288443	intron-variant	ATG16L2	GRCh38.p7	11:72825295	CCAACCTCCCCTTTC[C/T]CCACAGGATGCCCAC	89849
rs202178689	snp	C/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840890	ACAGGTCGCAGTTTG[C/T]CATATGAGGTCTCAG	89849
rs202200166	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829557	AAGTATGGGTTGGGG[A/G]ATTACGCTAGTTTTT	89849
rs367645022	snp	C/T	3.2962e-05	0.00405954	synonymous-codon, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827255	CCATATCATCATTAG[C/T]GGCCACAATGACCAG	89849
rs367835102	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824601	GTTGGGGAATGCTCT[C/T]GCTGCTCCTTGGGGC	89849
rs367875068	snp	C/G	6.59065e-05	0.00574012	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828752	GCTTCAAGTGTGGTT[C/G]TGACTGGACCAAAGC	89849
rs367967362	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72819966	TAGCTAGGATGGTTT[C/T]GATCTCCTGACCTCG	89849
rs367969271	snp	A/G			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829938	CTGAGGAGGGGCTGG[A/G]GGAGCTCTGAGGAGA	89849
rs368062723	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72825629	CAGATTTGCAGGATG[A/G]GGAGGGCTGAGTTCA	89849
rs368086033	snp	A/G	1.65187e-05	0.00287386	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826749	CAGCTGCCAAATTCA[A/G]GCTAACGAGGCACCA	89849
rs368123466	in-del	-/GA			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842252	GCTCTGACAGTGAGG[-/GA]GAGAGAGAGCCAGCT	89849
rs368134636	snp	C/T	0.000154888	0.00879886	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840858	TGCATTCGATAATCC[C/T]GCAAGATCAGAGACT	89849
rs368175073	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72819354	GCCCTGGAACACTCC[C/T]TTAGCACTCCCTGTC	89849
rs368243277	in-del	-/GC			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841365	AAAAAAAAAAAAAAA[-/GC]AAATGCAGTTTTTTT	89849
rs368260628	snp	A/G	1.7903e-05	0.00299185	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826264	GAACTCTGCCCCAGT[A/G]GCATGGGATTGTGCC	89849
rs368265647	snp	C/T	3.62457e-05	0.00425694	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843124	TCAAACGTGACCAAA[C/T]AAAGAGTGCCTTGTT	89849
rs368318423	snp	G/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815702	ACCCTGGGGGCTGAG[G/T]TGGGGTTTTCATGAG	89849
rs368329251	snp	C/G	0.000406587	0.0142523	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814572	CCGGCCTGTGAGTGC[C/G]CCCCGGTGCTGAGAG	89849
rs368454241	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840234	TCATTTGGGATAAAG[A/G]CTCAAGTCCTTAAGA	89849
rs368546416	snp	A/G	0.000153988	0.00877327	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826815	AGTGGGACCTCGGCC[A/G]TGCCTATTGTGAGCC	89849
rs368549136	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820993	GCCTCTGCGCAGGGC[C/T]TCTCGCTGCTGAGAC	89849
rs368710471	snp	A/G/T	3.29473e-05	0.00405864	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824131	TTCTGGAGTAAGTGT[A/G/T]TGTGTGCCTGTGTGT	89849
rs368728875	snp	C/T	9.88981e-05	0.00703131	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828732	GTCTGTCCTCAGGGC[C/T]GATGGCTTCAAGTGT	89849
rs368736333	snp	A/G	0.000199727	0.00999118	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841416	GTAGGTTTCTGAAGT[A/G]AAAATGCATTTAGAC	89849
rs368762555	snp	A/G	0.000265896	0.0115272	splice-acceptor-variant, intron-variant	ATG16L2	GRCh38.p7	11:72825300	CTCCCCTTTCCCCAC[A/G]GGATGCCCACCTCTC	89849
rs368822224	in-del	-/CCTGCAGGGAGGAGTCGGGCCTCGCC			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822338	AGGAAAGGCCCCGCC[-/CCTGCAGGGAGGAGTCGGGCCTCGCC]GGTGTCTGGAAGGGA	89849
rs368965663	snp	C/T	1.65012e-05	0.00287234	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828982	ACTACAGGGACCCCA[C/T]TGGTGAGCATGGCCT	89849
rs369064624	snp	A/G	0.000145217	0.00851982	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826275	CAGTGGCATGGGATT[A/G]TGCCCTCTCTGATCT	89849
rs369078861	snp	A/C	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72831969	TGTGCCCCCTGCCTG[A/C]TACCACGGGGGTAGA	89849
rs369120388	snp	C/G	4.95168e-05	0.00497553	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826537	ACCAGGTTTTAGCAG[C/G]AACTTACAACCAGGC	89849
rs369146874	snp	A/G	6.64628e-05	0.00576429	intron-variant	ATG16L2	GRCh38.p7	11:72816698	TGGGTATCTGTCTCT[A/G]CCCCAGGCTCACTCT	89849
rs369209148	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72830684	AGTCCAATCCTTTGG[A/C]GTTCCCCTGCTGCCT	89849
rs369278248	snp	A/G	0.000153988	0.00877327	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828311	CTTCCTGTCAGGAGT[A/G]GCCTGGCTAGGCTGT	89849
rs369303085	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842367	GTATGTCACATATAA[C/T]TTGGCATTTTGGTTA	89849
rs369306828	snp	A/G	5.21871e-05	0.00510792	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824814	TGTGTGTGGCTGCCC[A/G]ACTTCCTACCCGGGC	89849
rs369315223	snp	A/T	0.000268276	0.0115787	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841497	CAGGGAGCTCCTCTT[A/T]TCTGGGCTGGGGTAG	89849
rs369320489	snp	A/G	0.000182474	0.00955007	intron-variant	ATG16L2	GRCh38.p7	11:72816840	CTGGTAAGTGTATGT[A/G]GGTCCGTGGTCACAA	89849
rs369352973	snp	G/T	5.02475e-05	0.00501211	intron-variant	ATG16L2	GRCh38.p7	11:72825438	CTGCCGGCCAACTTG[G/T]TGCTTCTCTCCAGAC	89849
rs369367414	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822028	GGACCCGCTATCCGC[C/T]CTTTCCGTCCTCCAG	89849
rs369460248	snp	C/T	1.64939e-05	0.0028717	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826547	AGCAGCAACTTACAA[C/T]CAGGCTGCCCAGCTC	89849
rs369494820	snp	A/G/T	0.000120373	0.00775723	intron-variant	ATG16L2	GRCh38.p7	11:72817721	GCACTTGGGTGAACC[A/G/T]GGGGACATTGAGCAC	89849
rs369667021	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823368	AAGCTTGACTGAGCC[C/T]GTCTGTATGTGTGAA	89849
rs369676186	multinucleotide-polymorphism	CC/TA			intron-variant	ATG16L2	GRCh38.p7	11:72832255	TGAGCCCTTCTCTCC[CC/TA]CAAAACCTTCCCTTC	89849
rs369740786	snp	C/T	0.000115374	0.0075943	stop-gained, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828426	AGCCTCAGCCACGAC[C/T]AACTGCACCTGCTCA	89849
rs369900834	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72830719	AGACCACCCGCAACC[C/T]CAGCATGAAATCTGG	89849
rs369947367	snp	C/G/T	8.2367e-05	0.006417	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828885	GTGGCCACTACAGCC[C/G/T]GGACAGAAGCTATGC	89849
rs370065778	snp	C/T	0.000131898	0.00811982	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842612	TCAACTGTCTCCCCT[C/T]TCAGGTACCTGAATC	89849
rs370112019	snp	A/T	1.6625e-05	0.00288309	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825397	GATCCACCTCTGGAA[A/T]GTTGTGGGAAGTAAG	89849
rs370329191	snp	C/T	6.60197e-05	0.00574504	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826681	GCCAAACTCTTGATC[C/T]GTACCTGGGGCCGGG	89849
rs370361758	snp	G/T	4.94197e-05	0.00497066	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824063	GTTTTGTCTCAGGTC[G/T]GCCTCAGCCACCTCC	89849
rs370385881	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814850	TGCGTCCTCGGGTGT[C/T]GGTTTTGCAGGGTCT	89849
rs370391057	snp	C/T			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828174	GTCTAAGTTCCTCGA[C/T]GGAGGCAGCTGGCTG	89849
rs370451057	in-del	-/CAA			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72827976	AACAAAACAAAAAAA[-/CAA]AGCTAGAGCCAGTGC	89849
rs370497449	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823472	GCAGGGTCTCCTCCA[C/T]CCTTCTTGATTTGCC	89849
rs370509918	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72818979	TTGTTTGAGAGGTGA[G/T]TCTCAAACATCTGAC	89849
rs370540910	snp	C/G/T	5.83009e-05	0.00539885	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822567	GGGGATGGGCCGGTC[C/G/T]GACCCTTGCGTTCTG	89849
rs370575074	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838271	GGTTTCACTTTCTCA[A/G]TCTGGGGACTAACCT	89849
rs370640417	snp	A/G	1.66632e-05	0.0028864	intron-variant	ATG16L2	GRCh38.p7	11:72816686	CCAGGGGGCTGCTGG[A/G]TATCTGTCTCTGCCC	89849
rs370813789	snp	G/T	0.0452985	0.143518	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814432	AACGCGCCGCTAGGC[G/T]GGAGAGCGCGGCCAT	89849
rs370826665	snp	A/G	0.0232847	0.105357	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814941	GGTAGCGCAGTGAAA[A/G]AACGCGGGACTTGTC	89849
rs370830651	snp	A/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836574	AGGATATTACACCTA[A/G]CACATGGGGGCTTCA	89849
rs370849214	snp	A/G	1.68459e-05	0.00290219	intron-variant	ATG16L2	GRCh38.p7	11:72825269	AGACATGCGCGGGGA[A/G]GGCCGGGGCACCAAC	89849
rs370896555	snp	C/T	0.000115675	0.00760421	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826755	CCAAATTCAAGCTAA[C/T]GAGGCACCAGGCAGT	89849
rs370916472	snp	A/C	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823240	TCTGAATAGCTGTCA[A/C]CAGGAGAGAACCTGT	89849
rs370929444	snp	A/G	0.000153988	0.00877327	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841004	TACTTGAGTTGTTGA[A/G]CAATAATGCTGATGC	89849
rs370997742	snp	C/T	0.000101704	0.00713032	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822813	AGGGGCTGGCTTGGT[C/T]CCTTGGCCTTTCTGA	89849
rs371117094	snp	A/C	0.000670166	0.018293	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822468	CTCAGGATGCTTTTT[A/C]CCCAACAAGGGCCAA	89849
rs371207895	snp	A/G	1.64833e-05	0.00287078	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828733	TCTGTCCTCAGGGCC[A/G]ATGGCTTCAAGTGTG	89849
rs371236698	snp	C/G			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827710	TTGGGAGGCCGAGGC[C/G]GGCAGATCACCTGAG	89849
rs371279032	snp	C/T	9.89413e-05	0.00703284	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826596	CAGTCCAAGGTGAGG[C/T]CTGACTGGGGAGGCT	89849
rs371304735	snp	A/C	0.000153988	0.00877327	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826500	TAGCACCTCTCACTT[A/C]CTCTCCCATTTCTCC	89849
rs371387332	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72829081	GAGTCCCCAGCCCTT[G/T]TCCCTCCACCTTCCA	89849
rs371478932	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72830571	AACCCCTGGGTTTAA[A/G]CAATCCTCCCACCTG	89849
rs371530362	snp	A/G	3.30115e-05	0.00406259	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826637	CAGAGGTCATACCTC[A/G]GGACTAGGGGGCCTG	89849
rs371567047	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834874	ACAGGCGTAAGCCAC[C/T]GTGCCCAGCCATCAT	89849
rs371578822	snp	A/C	1.94365e-05	0.00311735	intron-variant	ATG16L2	GRCh38.p7	11:72826152	CCTCATTTCAACTGT[A/C]CCTTCCCCTGGTCCT	89849
rs371587704	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815799	GGAGGGAGCTAGGCC[C/G]GGACTTACCACCCCA	89849
rs371704907	snp	C/T	6.62921e-05	0.00575688	intron-variant	ATG16L2	GRCh38.p7	11:72816706	TGTCTCTGCCCCAGG[C/T]TCACTCTCTTGCACT	89849
rs371718185	snp	C/T	1.64792e-05	0.00287042	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842789	TCCCTCAGGAAAAGA[C/T]AACTCATCATCTGTC	89849
rs371779494	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72816348	CCAAAGGCCATTGAC[A/G]GGTAGAGCTCGGTTT	89849
rs371901824	snp	C/T	5.05038e-05	0.00502487	synonymous-codon, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829354	GAGCCACATGGTGAG[C/T]GTGGACCAGGGCAGG	89849
rs372026480	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72831230	CTCTTATTCAGGCTG[G/T]ATGCGGTGGCTCACG	89849
rs372118310	snp	C/T	0.00014556	0.00852989	intron-variant	ATG16L2	GRCh38.p7	11:72826166	TCCCTTCCCCTGGTC[C/T]TCCCAGGTCGCCTGG	89849
rs372205989	in-del	-/CTTCCTGT	0.0517242	0.152272	intron-variant	ATG16L2	GRCh38.p7	11:72819160	ATGAGGTGGGCTGTC[-/CTTCCTGT]CTTCCTGTGACTGCC	89849
rs372258795	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838754	AAACTCCAAGCCTGG[C/T]CTTGATTGTAGCAGT	89849
rs372293223	snp	C/G	0.000411743	0.0143423	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824078	TGCCTCAGCCACCTC[C/G]CTGACGCTGTCCCAC	89849
rs372298404	in-del	-/CAAAAA			intron-variant	ATG16L2	GRCh38.p7	11:72827952	AAACAAAACCAAAAC[-/CAAAAA]CAAAACAAAACAAAA	89849
rs372312861	snp	A/G	1.64751e-05	0.00287007	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824147	TGTGTGCCTGTGTGT[A/G]CACCCACGTGTGTGT	89849
rs372332271	snp	A/G	0.000153988	0.00877327	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840975	CTAAGGGAGAAAACC[A/G]AAGAAGCTCATTTTA	89849
rs372434092	snp	A/T	0.00398564	0.0444627	intron-variant	ATG16L2	GRCh38.p7	11:72817154	CCTTGCCTGATGCCT[A/T]AAGAAAGGGTCTTGC	89849
rs372441212	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840359	AATTGCAAAGTATCC[A/G]ACTGGATTACCGTGC	89849
rs372460060	snp	C/G	4.95193e-05	0.00497566	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826674	GGTCTTGGCCAAACT[C/G]TTGATCCGTACCTGG	89849
rs372481151	snp	A/G	3.39012e-05	0.00411697	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843143	GAGTGCCTTGTTTCA[A/G]TCTTTACCACTGGCA	89849
rs372509129	snp	C/G	1.64961e-05	0.00287189	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72816748	CATCTCTTAGAGAAG[C/G]CTGAGCTGCTGGACA	89849
rs372568353	snp	A/G			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821046	TGGGTGAGGCCAGGA[A/G]GCCAGCAGGGAGGGG	89849
rs372685355	snp	A/G/T	0.000165551	0.00909679	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841611	GAAGCGAGGTTACCC[A/G/T]GTGCTCCCCTCCAGG	89849
rs372774100	snp	A/G	0.000131939	0.00812109	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827202	GGCTCCAGGACCATC[A/G]ATGTCCTTTCCTACT	89849
rs372792786	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72832899	CAGTGACTTCCAGGC[A/G]CTCATATCCCCACCT	89849
rs372921987	snp	C/T	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72831244	GGATGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	89849
rs372974423	snp	A/G	0.000324842	0.0127403	intron-variant	ATG16L2	GRCh38.p7	11:72817888	CTGAAAATGGGGTAG[A/G]GAGATGTGGTCCAAG	89849
rs372993822	snp	A/T	0.00199481	0.0315187	intron-variant	ATG16L2	GRCh38.p7	11:72817935	GGGTACTCCTGTGTT[A/T]GCTGAATTCTCCAAG	89849
rs372997980	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835437	AGAGGTGGTGGTGAG[A/G]AGAGGTGGTGGTGAG	89849
rs373005839	snp	A/T	2.00214e-05	0.00316391	intron-variant	ATG16L2	GRCh38.p7	11:72824886	GGGCAGTGGTGAGAG[A/T]GTGCAGGCACAGGGG	89849
rs373092699	snp	C/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814078	TCTCGAACTCGGCCC[C/G]GGCGCGGCGGGGTTA	89849
rs373191976	snp	A/G	1.64893e-05	0.0028713	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826589	GGAGGCACAGTCCAA[A/G]GTGAGGCCTGACTGG	89849
rs373317721	snp	A/G	3.30066e-05	0.00406229	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826538	CCAGGTTTTAGCAGC[A/G]ACTTACAACCAGGCT	89849
rs373334602	snp	C/T	2.18233e-05	0.00330321	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841433	AAATGCATTTAGACC[C/T]ATGCCCAGGAGAACC	89849
rs373357084	snp	A/C/T	1.65872e-05	0.00287981	intron-variant	ATG16L2	GRCh38.p7	11:72828551	TGGCCTTTGCTGGGA[A/C/T]AGCTGAGCCTCTCTT	89849
rs373494327	snp	A/G	2.06503e-05	0.00321321	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841511	TATCTGGGCTGGGGT[A/G]GGGGCTGCTGGGAGG	89849
rs373543348	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813569	ACGCCGCCCAATGGG[A/G]TGAAGCGTCTGGCCC	89849
rs373581172	snp	A/G			splice-acceptor-variant, utr-variant-5-prime, intron-variant	ATG16L2	GRCh38.p7	11:72822846	TTCATTACCTCTCCT[A/G]GGGGCCCGGACACCC	89849
rs373641292	snp	C/T	1.6522e-05	0.00287414	intron-variant	ATG16L2	GRCh38.p7	11:72828990	GACCCCATTGGTGAG[C/T]ATGGCCTCCACCTGG	89849
rs373641875	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72818060	AGTGGGCTCCAACAG[A/C]AGCTGGAGGGAGTTA	89849
rs373737720	snp	A/G	3.295e-05	0.00405881	missense, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842634	ACCTGAATCTCTCTC[A/G]TCCATGGAGTGTCAC	89849
rs373804690	snp	A/G	1.67638e-05	0.0028951	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827338	GGGAGGGCTGGGGAC[A/G]GGGCTCCCAAGTTCT	89849
rs373847657	in-del	-/GC			intron-variant	ATG16L2	GRCh38.p7	11:72828603	GAGCCCTCCCTGGAG[-/GC]CCCTCCAGACCAGGT	89849
rs373855802	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840093	ATGCTGCTCCAGCCT[C/T]CTAATCGCTCCCTAT	89849
rs373884554	snp	C/T	9.89006e-05	0.00703139	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828446	GCACCTGCTCAGCTG[C/T]TCCCGAGACAACACA	89849
rs373921854	snp	C/T	0.00058987	0.0171635	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838893	AGCAGGAAACAATTA[C/T]GTAGTTTGTCAGTCA	89849
rs374002673	snp	C/G	0.00010068	0.00709434	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823003	GCTCTGAGCTGAGCC[C/G]CACCCCAGAGGCTGC	89849
rs374082496	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72831618	CCCAGCCCTCATGCC[C/G]TGGCTCCCAGCAGCC	89849
rs374108476	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822470	CAGGATGCTTTTTAC[C/G]CAACAAGGGCCAAGC	89849
rs374109742	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72819964	GTTAGCTAGGATGGT[C/T]TTGATCTCCTGACCT	89849
rs374112851	snp	A/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813002	TATAACTCGAACTCA[A/G]CTGGGGCTGGTGTCT	89849
rs374124705	snp	A/G	1.75234e-05	0.00295997	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826176	TGGTCCTCCCAGGTC[A/G]CCTGGAGGCCAACCA	89849
rs374182416	snp	G/T	0.000193106	0.00982424	utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814451	GAGCGCGGCCATGGC[G/T]GGGCCGGGCGTCCCC	89849
rs374206026	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828234	CAGCCTTTACCCCAG[C/T]GATCCAGGGCCCTGG	89849
rs374267897	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72831859	GAAGCCCTGCAGCTG[G/T]ACTGTGGCTGCATTA	89849
rs374287118	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72829138	AAGGTACTTTCCACA[C/T]GCACTTGGTTCCATC	89849
rs374319604	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72820025	GCTGGGATTACAGGC[A/G]TGAGCCACGGCACCC	89849
rs374361202	snp	C/T	1.66785e-05	0.00288773	intron-variant	ATG16L2	GRCh38.p7	11:72825288	CGGGGCACCAACCTC[C/T]CCTTTCCCCACAGGA	89849
rs374388715	snp	A/G	0.000153988	0.00877327	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840854	ACTATGCATTCGATA[A/G]TCCTGCAAGATCAGA	89849
rs374500366	in-del	-/TGCCTCC			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822581	CCGACCCTTGCGTTC[-/TGCCTCC]CGCCCCGCCTGCCTG	89849
rs374539842	snp	C/G			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814848	AGTGCGTCCTCGGGT[C/G]TTGGTTTTGCAGGGT	89849
rs374619076	snp	A/G			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814883	TTTGCCTCCCCACCC[A/G]GGCAGTCCCCGGGGT	89849
rs374634166	snp	C/T	0.000121203	0.00778374	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829396	CTGGCAGTAGGGCCA[C/T]GACCTGCCTGCCTGG	89849
rs374686890	snp	G/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72835075	GGGTTGATTGCATCA[G/T]GCATCAAGTCAGTTC	89849
rs374711175	snp	C/G			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820954	CCTGGCTCCCCGAGT[C/G]CATGCCTGATCTTAG	89849
rs374760952	snp	G/T	3.29582e-05	0.00405931	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828737	TCCTCAGGGCCGATG[G/T]CTTCAAGTGTGGTTC	89849
rs374838124	snp	G/T	1.90551e-05	0.00308661	intron-variant	ATG16L2	GRCh38.p7	11:72826156	ATTTCAACTGTCCCT[G/T]CCCCTGGTCCTCCCA	89849
rs374858526	snp	C/G/T	0.000165085	0.00908378	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823778	TAGGCCCCGGCTCAG[C/G/T]TTCCCAGGAACTTTT	89849
rs374888014	snp	C/T	0.000214704	0.0103589	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827302	ACAGCAGGTGACAGG[C/T]GCAGGCTGGGGGAGG	89849
rs374944114	snp	C/T	5.1813e-05	0.00508958	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826240	TGTGGACTTTGACCC[C/T]TCGGTGAGGAACTCT	89849
rs375034663	snp	C/T	8.23744e-05	0.0064172	intron-variant	ATG16L2	GRCh38.p7	11:72828820	CCAAGTGTGCCCTGC[C/T]GGACCCTGTGTGTGC	89849
rs375174814	snp	A/G	0.000153988	0.00877327	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828325	TGGCCTGGCTAGGCT[A/G]TTCCTCATCCCTGTC	89849
rs375195570	snp	C/G	1.64765e-05	0.00287019	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824020	CATTTGTACACACAC[C/G]AGCCAGTCCCTTAGC	89849
rs375424380	snp	C/T	8.26398e-05	0.00642753	intron-variant	ATG16L2	GRCh38.p7	11:72816720	GCTCACTCTCTTGCA[C/T]TCTCCAGATAACCAT	89849
rs375724989	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72830712	CCTTCAGAGACCACC[C/T]GCAACCCCAGCATGA	89849
rs375759503	snp	G/T	0.000546923	0.0165276	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828321	GGAGTGGCCTGGCTA[G/T]GCTGTTCCTCATCCC	89849
rs375819702	in-del	-/CCC			intron-variant	ATG16L2	GRCh38.p7	11:72831962	GGTGTGTGTGCCCCC[-/CCC]TGCCTGCTACCACGG	89849
rs375841521	snp	A/T			upstream-variant-2KB, intron-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812521	TTTAGTCAAAATCAA[A/T]CACTTCTTTATCATA	89849
rs375957423	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840448	TGAGGAGAGGTAACT[C/T]TGCAATAATATATTC	89849
rs375973734	snp	C/T	3.29647e-05	0.00405971	synonymous-codon, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827225	TTCCTACTGTAATGA[C/T]GTGGTGTGTGGGGAC	89849
rs375989927	snp	A/C/G	0.000402936	0.0141885	intron-variant	ATG16L2	GRCh38.p7	11:72817889	TGAAAATGGGGTAGA[A/C/G]AGATGTGGTCCAAGG	89849
rs376020271	snp	C/T			upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814100	GCGGGGTTAAGACAC[C/T]CGGGCCTTGAGGGCC	89849
rs376063409	snp	C/T	1.65007e-05	0.00287229	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826541	GGTTTTAGCAGCAAC[C/T]TACAACCAGGCTGCC	89849
rs376086779	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72818133	TAGCCTGCTCTGCTC[A/G]CTACTCCATGGCTCA	89849
rs376089151	snp	C/T	8.60919e-05	0.00656037	intron-variant	ATG16L2	GRCh38.p7	11:72817720	GGCACTTGGGTGAAC[C/T]GGGGGACATTGAGCA	89849
rs376155418	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72834901	TCATTCCATTCCTTT[A/T]CAATTGAGGATGTGG	89849
rs376208354	snp	A/G	0.000153988	0.00877327	intron-variant	ATG16L2	GRCh38.p7	11:72825267	AGAGACATGCGCGGG[A/G]AGGGCCGGGGCACCA	89849
rs376360091	snp	A/G	5.06308e-05	0.00503119	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817759	ATTGGTTGGCAGGGA[A/G]GAGTCAGAGCTTGAC	89849
rs376377691	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825542	GGGCAGTGACTAGAC[A/G]ATGCCTTGGAAAGAG	89849
rs376380363	snp	G/T	7.46714e-05	0.00610984	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838909	GTAGTTTGTCAGTCA[G/T]TTCCTGACTCAGTAT	89849
rs376409434	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835680	AAATCTAACAAAATT[A/G]AATACATACCTTTTT	89849
rs376481786	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72818597	TGAGAGTTGACTCCT[C/T]GCAGGCATCGGGCTA	89849
rs376493601	snp	C/T	3.32138e-05	0.00407502	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825389	GACCGCCTGATCCAC[C/T]TCTGGAATGTTGTGG	89849
rs376578895	snp	G/T	0.000153988	0.00877327	intron-variant	ATG16L2	GRCh38.p7	11:72828997	TTGGTGAGCATGGCC[G/T]CCACCTGGCCACCTG	89849
rs376664808	snp	C/G	0.000131785	0.00811635	intron-variant	ATG16L2	GRCh38.p7	11:72828877	GCTCTGCTGTGGCCA[C/G]TACAGCCCGGACAGA	89849
rs376735962	snp	C/T	0.0010855	0.0232716	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841587	GGAAGGAGAGATCTG[C/T]AGCAAAGGGAAGCGA	89849
rs376832672	snp	G/T	2.05821e-05	0.0032079	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822573	GGGCCGGTCCGACCC[G/T]TGCGTTCTGCCTCCC	89849
rs376864965	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72833446	GGGTCCAGAAGGTGA[A/T]GGGATGAGCCTCAAG	89849
rs376985892	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842303	TTAACCACAGAGCAA[C/T]GCCTTCCCTCTTCGG	89849
rs377044129	snp	A/G	1.64838e-05	0.00287083	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828468	GACAACACACTCAAG[A/G]TCATCGACCTGCGTG	89849
rs377117989	snp	A/C/T	4.35713e-05	0.00466735	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841437	GCATTTAGACCCATG[A/C/T]CCAGGAGAACCCTTA	89849
rs377168281	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72831937	GCTGCGGGGCATGCC[C/T]CCTCCCCCAGGGTGT	89849
rs377221319	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72831286	CCAAGGAGGGCAGAT[C/T]ACCTGAGGTCAAGAG	89849
rs377281883	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840105	CCTCCTAATCGCTCC[C/T]TATATCCTTTCTGCC	89849
rs377297513	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72816635	CCTAGCATCTCTGGG[C/T]TCCTTCAGCCCTTTT	89849
rs377424006	snp	C/G	1.70997e-05	0.00292396	missense, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72826190	CGCCTGGAGGCCAAC[C/G]AGACCCTGGAGGGAG	89849
rs377431219	snp	C/T	8.49697e-05	0.00651749	synonymous-codon, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829309	TTTCCCCAGCGCTGC[C/T]GTCAACGCCGTGGCC	89849
rs377583611	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837465	ATTTCTTAACCAAGG[-/A]AAAAAAAAAAAAAAC	89849
rs377584404	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72831730	AGCCACCGTGACTGA[A/G]CCCTTAGGAGGTGCC	89849
rs377664209	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823205	TTGGGATCAGAGCTC[C/T]GGGGGTGGGGAGTCA	89849
rs377697639	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823562	TTCCTTGCAGGTCCC[C/T]GGTGTCCAGGCCTTG	89849
rs377758400	snp	C/T			intron-variant, missense	ATG16L2	GRCh38.p7	11:72824680	GGAGCTGGAGGCTCC[C/T]ACCTGAGAAGGACTT	89849
rs386374138	in-del	-/ATCT			utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829591	GTATTTTTATCTCTA[-/ATCT]TCTCCTCACTTTTTC	89849
rs386374139	in-del	-/CATT			intron-variant	ATG16L2	GRCh38.p7	11:72830796	CCTTGCTATTCATTC[-/CATT]ATTCATTTACTCATT	89849
rs397810124	in-del	-/T	0	0	intron-variant	ATG16L2	GRCh38.p7	11:72834900	TCATTCCATTCCTTT[-/T]ACAATTGAGGATGTG	89849
rs397848860	in-del	-/GTCT			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828159	TTCAAATCAAAGTCT[-/GTCT]AAGTTCCTCGATGGA	89849
rs397954866	in-del	-/T			intron-variant	ATG16L2	GRCh38.p7	11:72833945	AATTTTTTTTTTTTT[-/T]CAGGAAAATATTCCC	89849
rs527297703	in-del	-/A	0.000322619	0.0126967	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842848	CAAAACATACTAGGG[-/A]GCAAGAGAAAAACAA	89849
rs527300920	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838217	TGTGCGTTAATGCAA[C/T]TGGTGCTAAATTCAG	89849
rs527468428	snp	A/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830304	ACCACTCACTACTTT[A/T]GGTCTAGCTGCCTCC	89849
rs527543577	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72818798	AACAATAAACAAGAC[C/T]TGGCCCCATGGGGCT	89849
rs527607769	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819526	TACTACCTCTGTCCC[C/T]ATGGTTAGTGCGCTG	89849
rs527713447	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812983	TGTGATAACTGGTGA[A/C]GGTTATAACTCGAAC	89849
rs527877908	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839869	CATTCGGCAAGAGTG[C/T]GTTCAACAACTTCAA	89849
rs527882811	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831138	CTTGGAAGAGGCCAG[A/G]ATGGGAATAGATTAT	89849
rs527897973	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840550	CAAATAGAGGCCTGG[A/G]AAATTAAATGCTTAC	89849
rs527959316	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831683	CATTCCCGTTTCCAG[G/T]GACACATGGCTGGGG	89849
rs528106873	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815981	AGTTGGGATTATTTA[C/T]TTATTTATTTATTTG	89849
rs528134078	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838103	AAGATGTGGCTACTA[A/G]TTCAGCCCCTCCATA	89849
rs528182415	snp	A/T			intron-variant	ATG16L2	GRCh38.p7	11:72817970	GTGCTGCAAGCATTG[A/T]GTGAGCCCTAGTGTG	89849
rs528300416	snp	A/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72835152	AGTTAGCTGAGCTTT[A/G]CCCTTGGTCACAGAC	89849
rs528348540	snp	A/C	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72836175	GTGGGGCCCTTCCCC[A/C]AACAGGCTGTGTCCT	89849
rs528526102	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816637	TAGCATCTCTGGGCT[C/T]CTTCAGCCCTTTTAG	89849
rs528584658	snp	A/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72817150	TGTTCCTTGCCTGAT[A/G]CCTAAAGAAAGGGTC	89849
rs528812501	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72819442	CATTAAAGACAAGCA[A/G]TACACAAAACATGCT	89849
rs528913363	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825703	TCCTACAGGGACAGG[C/T]CCTTGAAGAGCAGGT	89849
rs528913420	snp	A/C	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819768	TTTTTTTTTTTGAGA[A/C]GGAGTCTCACTCTGT	89849
rs528974603	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819995	CGTGATCCACCCACC[C/T]TGGCCTCCCAAAGTG	89849
rs529125082	snp	G/T			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829680	ATGGTACAGAGACCT[G/T]TGGGCTAGTGGGCTC	89849
rs529295576	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841287	TATGAGCCGTGATCA[C/T]GCCACTGAACTCCAG	89849
rs529343015	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842014	GGGTCACAATCACCA[A/C]GCAAACAAGATCGGC	89849
rs529344213	snp	A/G	0.00199481	0.0315187	intron-variant	ATG16L2	GRCh38.p7	11:72819895	GGACTACAGGCGCCC[A/G]CCACCATGCCCGGCT	89849
rs529556043	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826916	CTCTCTGGGAGTGGC[C/T]CTGAGATTCATAGGC	89849
rs529570599	snp	G/T	0.000399281	0.0141238	missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72821730	GTCGGAGCTGCAGCA[G/T]AGGCAAAGCAGGTGA	89849
rs529725070	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837477	AAGGAAAAAAAAAAA[A/C]AACAAACCACAACCG	89849
rs529960861	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829506	ATTTAATGGGGAAGA[A/C]GGCCTGGCAGGACCT	89849
rs530465127	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821594	GCAGCCGACTCCCTT[A/G]GCGCCTTCGGCCCCG	89849
rs530498746	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826894	AGGGCACAAGGGACC[G/T]CACCTGCTCTCTGGG	89849
rs530701542	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72820356	TCTTTCTTATTACCC[A/C]TTTTTAGTCACATTC	89849
rs530741137	snp	A/G	3.3012e-05	0.00406262	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843180	TTGAGGCTGCCTGAA[A/G]CGAGTTCTGCTTCCG	89849
rs530805207	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72835078	TTGATTGCATCATGC[A/G]TCAAGTCAGTTCCTG	89849
rs530819424	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72836101	AGAGTCTTATGCACA[A/G]GATAATGTCTGGAAA	89849
rs530840345	snp	C/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843054	ATTATAGGACAGGAG[C/G]AAAGTTGTGCTTTTT	89849
rs530992036	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823162	ATCTCACCCCCCCAA[C/G]CCCTACCCTCAACCC	89849
rs531002879	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822673	GTGGTCGGAGCCCAC[A/G]AGACACCTGCAGAGG	89849
rs531054955	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816594	AGGCACAGGGCAGAG[A/G]CCAGCCTGCCAGAAG	89849
rs531059140	snp	A/C			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815688	CTGGGTGCTGCAGTA[A/C]CCTGGGGGCTGAGGT	89849
rs531189477	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72817081	GTCCCATCTCCTTCC[C/T]GTCCCACCCCTATAC	89849
rs531195228	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72816245	TCGGCCTCCCAGAGC[A/G]CTGGGAATTCAGGTG	89849
rs531211698	snp	A/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72830441	ACCTTCTAGACCTGC[A/G]GTCTCCCCATCCAAT	89849
rs531224111	in-del	-/A	0.00438332	0.0466095	intron-variant	ATG16L2	GRCh38.p7	11:72830518	GCTTTTGAGACACAC[-/A]AAAAACCTTAGTGCA	89849
rs531275476	snp	A/G	1.79326e-05	0.00299432	missense, synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824834	CCTACCCGGGCTCAG[A/G]ATGTGCTGGTAAGGG	89849
rs531438698	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837377	TGGCGAGCATTTCAA[A/G]TTTTTTAAGATTCTT	89849
rs531458254	snp	A/G	0.00358779	0.0422022	intron-variant	ATG16L2	GRCh38.p7	11:72819947	AGATGGGGTTTCACC[A/G]TGTTAGCTAGGATGG	89849
rs531597135	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813124	CCAAACATCAGGCTC[A/G]GCCTGTGCAAAGGCC	89849
rs531618304	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841760	AAGCTCCAATTTTGC[A/G]TTGCACTTCACTTTT	89849
rs531661363	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813836	TCTTCTCGAGGCCTA[C/G]AGTCCCTCTCTCCCT	89849
rs531801331	in-del	-/AGTCTGGGCCCTGGCTCC	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820930	GCTGTTCCCATATTG[-/AGTCTGGGCCCTGGCTCC]CCGAGTCCATGCCTG	89849
rs531859118	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840601	TAGCCCGCTTTAATG[C/T]TCATAAAGTTTGTTC	89849
rs532011361	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826388	TCCTCCTCCTTGGGC[C/T]GGAGGCTCCTTTGCC	89849
rs532041123	snp	A/C	0.000633692	0.0177889	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842583	GGAGCAATTTTCTTT[A/C]AACATCTTTTAATTC	89849
rs532201176	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72818847	ACTGTGATAGCCCAG[A/G]AAATACACATCCAGT	89849
rs532348821	snp	G/T	0.00358779	0.0422022	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837323	AAAAATTTCTTCAGT[G/T]ATCACCTTACTTTTG	89849
rs532411146	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817297	CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT	89849
rs532549331	snp	A/G	0.000475384	0.0154099	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841601	GCAGCAAAGGGAAGC[A/G]AGGTTACCCGGTGCT	89849
rs532590002	snp	C/T	3.52299e-05	0.00419687	utr-variant-5-prime, missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72817838	GAGGAGGAGGGGCTC[C/T]GGCTGGTCTGTGGTG	89849
rs532814371	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72820036	AGGCGTGAGCCACGG[C/T]ACCCGGCCTTTTCTT	89849
rs532826258	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820970	CATGCCTGATCTTAG[C/G]CTTGTGTGCCTCTGC	89849
rs532924529	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72830319	TGGTCTAGCTGCCTC[C/T]TGGCCATCATCTCCC	89849
rs532927825	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825774	GCTCTCAGAACTCAG[A/G]TAAGAGACAAGTATG	89849
rs533087423	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841395	TTTTGCCCTTCAGGC[A/G]AATATGTAGGTTTCT	89849
rs533147842	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842133	TTTAAAGGCTGTTTC[C/T]CTGTGATGAACTAAG	89849
rs533159367	snp	A/G	0.0011165	0.0236009	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843101	ACTCCAGGGCAATAC[A/G]GTTTAGGTCAAACGT	89849
rs533219666	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834882	AAGCCACCGTGCCCA[A/G]CCATCATTCCATTCC	89849
rs533340953	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827627	AGACCCTAACTTTGG[A/G]CTTGAATTGTTTGTA	89849
rs533399984	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822608	CGCCTGCCTGCGGCG[A/T]CCCAGGCTGCCGACT	89849
rs533431248	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827009	CTGTCTGGTTTCTTG[G/T]TGACCTCAGGCTGTG	89849
rs533618130	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816091	TCACGCCTGTCTCCC[A/G]TCTCAGCCTCCCGAG	89849
rs533636867	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823134	TTGTCTGGAGCCACT[A/T]GGGGTCAGTTCCATC	89849
rs533691668	snp	A/C	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816476	GCAGTGGTCATCCTT[A/C]TGTCCCTGGGAGAGC	89849
rs534059616	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829905	CCACCTGCTTCAGGC[A/T]CTCAGGGTAGACTGA	89849
rs534187018	snp	C/T	0.00199481	0.0315187	intron-variant	ATG16L2	GRCh38.p7	11:72819131	TATTTGTAGACTAAG[C/T]GATGAATGAGGTGGG	89849
rs534284309	snp	A/C/G			intron-variant	ATG16L2	GRCh38.p7	11:72818155	CATGGCTCACCCCTC[A/C/G]CCCAGCCATCCCCAA	89849
rs534394182	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830595	CCACCTGGTCTTCCC[A/G]AAGGGCTGGGATTAC	89849
rs534419333	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72826026	TCTCCAGCCCAGGCC[C/T]GCAGAACAGACCCAG	89849
rs534527439	snp	A/G	4.94776e-05	0.00497357	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827203	GCTCCAGGACCATCA[A/G]TGTCCTTTCCTACTG	89849
rs534579467	snp	C/G	0.00088589	0.0210276	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822383	TCTGGAAGGGAGGGG[C/G]GCAGCAGCCGCCCCC	89849
rs534623034	snp	A/G	2.20053e-05	0.00331695	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841557	CAGTGGAGGCAGGGA[A/G]GCGTGTGGCTTGGGG	89849
rs534666788	in-del	-/G	0.00716266	0.059414	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821397	GAGCGGGTTGCTCTT[-/G]GCCAGAGAGGTTCCT	89849
rs534683679	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822723	CTGCATGCGTGACCG[C/G]TGCACGTGTACACCC	89849
rs534683991	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815724	TTTCATGAGAACTAG[A/G]CCAGGCCCAGGGCCT	89849
rs534700170	snp	G/T	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827597	AAAAATTCTTTTAGC[G/T]GTTTTTTAAACCAAA	89849
rs534742598	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842525	CCGGTGAGGGTAAGG[A/C]AGAGACTGCAGCCCA	89849
rs534743238	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816232	TGATCCGCCCGCCTC[A/G]GCCTCCCAGAGCGCT	89849
rs534749896	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72833128	TTCAGTCTGCTGTTG[C/T]GCTGAGTGTCTCCCA	89849
rs534893300	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827789	ACTAAAAATATTAGC[C/T]GGGTGTGGTGGCAGA	89849
rs535065753	snp	G/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72824900	GAGTGCAGGCACAGG[G/T]GTGGTCTCGGCACCA	89849
rs535139538	snp	A/G	0.000145275	0.00852152	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72821703	GAAGGGCGCGGCCCT[A/G]GGCACGCTGGAGTCG	89849
rs535403649	snp	A/G	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72825176	AGTGTGGACAGAGAA[A/G]CTGGGGAGGGAGATA	89849
rs535478599	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819003	ATCTGACCCCCACAC[C/T]ACCCCCAGCCTCTGG	89849
rs535488392	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812585	CCTAGGTGTATTTTG[G/T]GAGTCAAAAAAGGAT	89849
rs535490507	snp	G/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839719	ACTCATTTTTGCTGA[G/T]TTTTGGGGATCTGGG	89849
rs535598467	in-del	-/CTT	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812524	AGTCAAAATCAATCA[-/CTT]CTTTATCATATACTA	89849
rs535734266	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814508	CCACATCGTGCGGCA[A/G]CTGCGGCTTCGGGAC	89849
rs535777373	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840100	TCCAGCCTCCTAATC[A/G]CTCCCTATATCCTTT	89849
rs535841740	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831393	TGCCTGTAATCCCAG[C/T]TACTTGGGAGGCTGA	89849
rs535866208	snp	A/T	0.00835141	0.0640778	intron-variant	ATG16L2	GRCh38.p7	11:72835605	CTCCTGGCTCCTAAG[A/T]CCATATGCGGTTGGT	89849
rs536043541	snp	C/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72820424	TACTAATCTGTTTTC[C/G]ACTTCTACTACTTGA	89849
rs536093225	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814085	CTCGGCCCGGGCGCG[G/T]CGGGGTTAAGACACC	89849
rs536102643	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821153	TTAGCTACGTGACTT[G/T]GGGCAAGACACTTAA	89849
rs536115700	snp	A/T	0.00106025	0.023	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72824759	AGGAGAGGTCACTCA[A/T]TTGGGGGAGCCCCTG	89849
rs536252962	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836370	CCAGTGGTCACATCC[A/G]GCAAGGGGACTTCAG	89849
rs536260330	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827920	CCTGGGCGACAGAGC[A/G]AGATGTCTCAAAACA	89849
rs536325396	snp	A/G	0.000198049	0.00994914	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828359	GTCCTTGTTCCTCAG[A/G]GGGCCCCACTGCACC	89849
rs536383328	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837767	ACGGAAATGTCAGGG[G/T]AGTGGGACCTGGAAG	89849
rs536424929	snp	A/C			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813354	GGATGTTCAAGTCTG[A/C]CAACACTCAGAGGGC	89849
rs536496579	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823527	GCGCCATTCCCCAGC[C/T]TAACACCTCTTCTCA	89849
rs536675609	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835879	TCAGCCTCCAGAGTA[A/G]CTGGGATTACAGGCA	89849
rs536695784	snp	C/T	0.0023933	0.0345097	intron-variant	ATG16L2	GRCh38.p7	11:72817032	TTTAGAATCTCTTTC[C/T]CCTCCACCTTTCTTT	89849
rs536856809	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832995	CATGAGGACCATGGC[C/T]TCTGCCTGCCCTGCC	89849
rs536881382	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72817296	GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC	89849
rs536920197	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834017	TTTGGCCTCTGGGAC[C/T]GAGGGAAAATAGTCT	89849
rs537056267	snp	A/G	0.000399281	0.0141238	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822206	ACTGCGCAGGCTCCA[A/G]GAAGAGGCGCGCGAC	89849
rs537185229	snp	G/T	3.32049e-05	0.00407448	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840895	TCGCAGTTTGCCATA[G/T]GAGGTCTCAGGAGTA	89849
rs537346883	snp	A/C			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813591	GTCTGGCCCTGAGTC[A/C]GGATGCTGGGGTGCT	89849
rs537435253	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821306	ATTTGGCAGCCTCTG[C/T]GCGAGGAGTCCTCGC	89849
rs537441992	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829677	TTCATGGTACAGAGA[C/T]CTTTGGGCTAGTGGG	89849
rs537545331	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839382	TAAGCAATATCAGAT[C/T]TGCGAAAAGATGACT	89849
rs537851900	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824510	TCTTTGCACCCACCA[A/G]CCCTACCCTGCTCCT	89849
rs537869148	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840069	ATCTTGCCACCACTT[C/G]TTTCTTGGATGCTGC	89849
rs537913300	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72818270	CCACCTGACACTACC[A/G]CCTTCCCTGCCCCTT	89849
rs538040771	snp	A/C			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827822	CCTGTAATCGCAGCT[A/C]CTTGGGAGGCTGAGG	89849
rs538119067	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72818332	ATGCTCTCCTGGTTT[C/T]CCTCTCATTTCTGTG	89849
rs538119554	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813464	AGAGCTGGCTCTCTA[A/G]CATCTAGCTAGAGAC	89849
rs538125151	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72820205	CATCTCCTGCTGGCT[A/G]CATCTTACATAACTA	89849
rs538195524	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839216	TTTCAGTGTGTCTTG[G/T]GTAGAGAGTTACAAA	89849
rs538258898	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830627	GGTGCACAGCACCAT[C/G]CTCGGCCCAACAGGG	89849
rs538427308	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825501	GTCTTGGATCTCTTT[A/G]TGTTTCTCTATCTGG	89849
rs538437761	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819838	GCAACCTCAGCCTCC[C/T]GGGTTCACGCCATTC	89849
rs538444678	snp	C/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72825979	GACTAGCTGTCCCTG[C/G]GACCCAGTGCCAGCA	89849
rs538448260	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827890	GTGAGCCCAGATTGC[A/G]CCACTGCCGTCCAGC	89849
rs538460355	snp	A/G	0.00165115	0.0286854	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822937	TGGAGAAGGAAGCTT[A/G]TGAGAAGTGGAAGAG	89849
rs538481822	snp	C/G			missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72822906	ACTCTGGCTCTGGCC[C/G]CTGAGCCAGAGCCCC	89849
rs538626114	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816668	CCGGAGATAAATTGC[A/G]TGCCAGGGGGCTGCT	89849
rs538655412	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834240	AAAATAAATGCGAAG[A/G]TTCAGAGCAGCTGGA	89849
rs538769652	snp	A/G	0.00318978	0.0398085	intron-variant	ATG16L2	GRCh38.p7	11:72835398	AGGTGGTGGTGAGAA[A/G]AGGCAGGAGAGGTGG	89849
rs538801990	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836821	ACTGTAAAGAAAGCA[C/T]ATCTGCACAGAGGCT	89849
rs538864187	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837737	TCCTCCACGAGCCAC[C/G]AGGTTCTTCCTTCCA	89849
rs538890214	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823212	CAGAGCTCTGGGGGT[A/G]GGGAGTCAGGCTTCT	89849
rs538976931	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72829160	GGTTCCATCCTTTCC[A/G]CAGCCCTGTGAGCTA	89849
rs539021809	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819815	CAGTCGCGTCATCTC[A/G]GCTCGCTGCAACCTC	89849
rs539096623	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813429	CCCTCCTTTCGTGTC[C/T]CACAGTAGCCTGAGC	89849
rs539436185	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832898	ACAGTGACTTCCAGG[C/T]GCTCATATCCCCACC	89849
rs539449994	snp	A/G	1.70499e-05	0.0029197	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826470	TCTGTGGCCCGAAGA[A/G]TGTTGCCTCCGGCTT	89849
rs539513368	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72821218	AGTGGCAGTACCAGC[C/T]TCCTGGTGTGGTGAG	89849
rs539809593	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72826068	TCTAACCTGGGGATG[C/T]GTCGGGGGGTGGGGC	89849
rs539823846	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838513	CATATAAAAACAGAC[C/T]ACTGTTAGGCATGAG	89849
rs539990968	snp	C/T			intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822778	TTCCTGTCTTCAGCG[C/T]ATCCTGTGCTGGGGT	89849
rs540015948	snp	A/G	4.34358e-05	0.00466004	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814595	GCTGAGAGGATGGCG[A/G]CTGAGGGGACGCGGC	89849
rs540061346	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827516	TGCTGGACTCCGCCT[A/G]GACCTTGCAACCAAG	89849
rs540077780	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815330	CTAATCTTGGCCAAA[A/C]CCCCACAATCAAATC	89849
rs540213343	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828769	GACTGGACCAAAGCT[A/G]TGTTCAGGTATGTCC	89849
rs540222162	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823067	TTGGGTTGGGAGGGG[C/G]CTTGAGGAGAGGCCA	89849
rs540233801	snp	A/C	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72816458	CTCAGCGGGCAGTAC[A/C]CCGCAGTGGTCATCC	89849
rs540260970	snp	A/C			intron-variant	ATG16L2	GRCh38.p7	11:72818915	GCATAGGTACGGACT[A/C]ATTTGAGAACCTTTC	89849
rs540293199	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816927	CTAGTGCCTCATCAG[C/T]CCTTGGCTGCTGCCC	89849
rs540417017	snp	A/C	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817691	TTTCATGTAGCATCA[A/C]TTGGGTGCCTTTGGG	89849
rs540461443	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824627	GGGGCCATGTTCTGC[C/T]GCCTGCCATGTCTGC	89849
rs540570583	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837146	ATCTTAAAAAAACCA[C/G]CCTTTTAATTTCTTT	89849
rs540584639	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837968	AGAAGAGTATATGCT[C/G]TAAAAATTAAGATGA	89849
rs540762693	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826300	TGATCTCCACACTGG[A/G]CAGGTGGGGGCTGTG	89849
rs541169568	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843023	AGGACAAACGTGACC[A/G]TATAAAGAAAAGCAT	89849
rs541232919	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814305	GGCCTTCGGTCCTCC[C/G]CGCCAAAGCCCTCTT	89849
rs541251360	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842029	CGCAAACAAGATCGG[C/T]AAACACGTTCCTTCT	89849
rs541579422	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72831885	CATTACACATACTCT[C/T]TTTAAAGCAACGTGT	89849
rs541627703	snp	C/T	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72835780	TGAGACAGAGTTTCA[C/T]TCTTGTTCCCCAGAC	89849
rs541737314	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827949	CAAAAACAAAACCAA[A/C]ACCAAAAACAAAACA	89849
rs541793322	snp	A/C	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830724	ACCCGCAACCCCAGC[A/C]TGAAATCTGGAGCCC	89849
rs541906595	snp	A/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72818552	AAAATCAGGCTCACC[A/T]TCTCCCCCAGAATTT	89849
rs542016223	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815093	CCCTGTCAGCCTACC[C/T]AGCCTGAGGGGGCAT	89849
rs542031385	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830288	CTCTGCTGACTCCCA[A/G]ACCACTCACTACTTT	89849
rs542034694	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813575	CCCAATGGGGTGAAG[C/G]GTCTGGCCCTGAGTC	89849
rs542244117	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825198	AGGGAGATACCACGT[C/T]TGCAGCAGGCTGTGT	89849
rs542280229	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816280	CCACCGCGCCCGGCT[G/T]GGGATTATTTTTAAG	89849
rs542300319	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841781	CTTCACTTTTTCCTC[C/T]TACAGATCTCATCAC	89849
rs542315775	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72819870	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	89849
rs542551570	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840497	CTTTAAGGCCATGAA[A/G]TTAGCTTATTATTTC	89849
rs542700790	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72833001	GACCATGGCCTCTGC[C/T]TGCCCTGCCCAATCT	89849
rs542716664	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822987	AGGTGACAGTCTCAG[A/G]GCTCTGAGCTGAGCC	89849
rs542749997	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72828632	GGTCCTGCTGAGGTA[C/T]CAAACCCCTCGACAA	89849
rs542823542	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823951	GTTCTTATCCCAGAC[C/T]TGAGAGGTTACAAGC	89849
rs543032403	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836962	TTAGCAGCTCTTCCA[A/G]AAAATATTTTAAAAT	89849
rs543145692	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831557	AGTCTAACGGTCTAA[A/G]AGCCTTGGGCTCCAA	89849
rs543264335	snp	C/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72835995	TCAAGTGATCTGCCC[C/G]CCTCGGCCTCCCAAA	89849
rs543279116	snp	A/C	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72817649	TCCATCTTCCCAGGA[A/C]GAAGTTAATGGCTCT	89849
rs543321228	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820830	GTCTCTCCCACCGAC[C/G]CTGCTTGGCTCTGGG	89849
rs543435462	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814251	CCGGCGGTTCAGACC[C/G]GGAGGCGGCTCCTCC	89849
rs543608961	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841856	CTCTCTAGGGTTCTA[C/T]TGAAAATGTACCAAA	89849
rs543843025	snp	A/C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814761	AACCTGGACGAGCCC[A/C/T]TCCTGGTCCCCCTGC	89849
rs544054434	snp	C/T	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72833339	ACTCATCACAAACAT[C/T]TTCAGCTTATCTGTA	89849
rs544163827	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826895	GGGCACAAGGGACCT[C/T]ACCTGCTCTCTGGGA	89849
rs544173451	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72830075	TCTTCCTCCAGGGGT[A/C]GTGCCCAGGGTGGGG	89849
rs544189194	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817011	GGCCTTCCCACAGGA[C/T]AGCTGTTTAGAATCT	89849
rs544408951	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812777	GGAATTCATCACTGT[C/T]ATCAGCTGGCCCTGG	89849
rs544552512	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838538	CATGAGGGCTGCCCC[C/T]CTCTTTGCTCCTAGG	89849
rs544552620	snp	A/G	0.000685203	0.0184968	utr-variant-3-prime, intron-variant, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72829436	CTTGCCCGAAGCCTG[A/G]AGCTTCCTTCGGCGC	89849
rs544942684	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826323	GGGCTGTGGGACCTG[A/G]GGGCGCAACATGGAT	89849
rs544976413	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72833294	ACATATCCATGCCTG[A/G]ATACAGGCTCTTCCA	89849
rs544982429	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72833951	TTTTTTTTTTCAGGA[A/G]AATATTCCCAGACCA	89849
rs545028664	snp	C/T			synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828506	CATCCGCCAGGTGTT[C/T]AGGTACCAGCCTCAT	89849
rs545152613	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828041	CCAGCAATTACTGTT[C/T]GCAACCCTTCCTTCT	89849
rs545290399	snp	C/G	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823157	GTTCCATCTCACCCC[C/G]CCAACCCCTACCCTC	89849
rs545472967	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838727	AAAGGTGCCTAAAAA[A/T]CAAGACTGGCCAAAC	89849
rs545537336	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839475	AGACTTTTGTAATCC[C/T]CTGAATGAGAGTTGA	89849
rs545615442	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814270	GGCGGCTCCTCCCGG[A/T]GGCAGATCCTCCCGG	89849
rs545652423	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832785	TTCCTGCTTTTCTAA[A/G]AACTGGATTCAGATT	89849
rs545714353	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823325	CAAGCATGTGCATCC[A/G]CAGGGACATGAGGCC	89849
rs545746508	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816505	GCAGGTCCTCTTCCA[C/T]GTGGGCCTGGGGACC	89849
rs545936230	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819846	AGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT	89849
rs545938917	snp	C/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72830786	CATCTTCATTTCCTT[C/G]CTATTCATTCATTCA	89849
rs546147526	snp	C/G	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72819564	TCCAAAGCTCCTAGC[C/G]TGGCTCCCCCGTCGA	89849
rs546209060	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819903	GGCGCCCGCCACCAT[A/G]CCCGGCTAATTTTTT	89849
rs546214659	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72835312	TATGACAACTCTGTG[C/T]GTTACTATGGGCCTG	89849
rs546284520	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814169	CCCGGAGGCTCCGAC[C/G]TCGCTCCTGCTTATG	89849
rs546474256	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72825096	TAGAGTAGCATAGCA[C/T]GGAGGCTGCTGCAGG	89849
rs546496996	snp	C/T	3.6632e-05	0.00427957	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841000	ATTTTACTTGAGTTG[C/T]TGAGCAATAATGCTG	89849
rs546537220	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820955	CTGGCTCCCCGAGTC[C/G]ATGCCTGATCTTAGC	89849
rs546559006	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827826	TAATCGCAGCTACTT[A/G]GGAGGCTGAGGCAGG	89849
rs546603017	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823457	CTTGGGTGCCTGTCC[A/G]CAGGGTCTCCTCCAT	89849
rs546607595	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72816035	CCAGGCTGGAGTGCA[A/G]TGGTGTGATCTCCGC	89849
rs546712975	snp	C/G			intron-variant	ATG16L2	GRCh38.p7	11:72818751	CTCTCAACATCTGTT[C/G]ACAGTTGCTATATCC	89849
rs546854689	snp	A/G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72836223	GCTGGAAGCCAGGGG[A/G/T]ACTCAGCCTTTGACT	89849
rs546892677	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837700	GCGCAATCCTTCAGT[C/T]CTTTCTCATAGAAAG	89849
rs547002915	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825739	AGTCTACCAGGTGAC[C/T]CTCTTCTAGCATCAC	89849
rs547002971	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819776	TTTGAGACGGAGTCT[C/T]ACTCTGTTGCCCAGG	89849
rs547101480	snp	C/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813160	CGTCTAAGACAATGA[C/T]ATGTGGGGGACTGAG	89849
rs547274238	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814021	TGGGTCCCTGGCTGG[C/G]TGCGCGGCCAGGAGC	89849
rs547289366	snp	C/T	0	0	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840699	GTAGATTAAATGTCC[C/T]GAGATGAGTTGATTT	89849
rs547505893	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813363	AGTCTGCCAACACTC[A/G]GAGGGCAGGGCCTGC	89849
rs547722116	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72835596	AACCCAGACCTCCTG[A/G]CTCCTAAGTCCATAT	89849
rs547908984	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72833538	TGTTCCTCACAGGAG[C/T]AAGTGGTGAAGAGTG	89849
rs548035295	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72817074	TGCATTTGTCCCATC[C/T]CCTTCCCGTCCCACC	89849
rs548244847	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837531	TATTGTGCTCCCTAC[A/C]TTCTACAGGAGCGGA	89849
rs548327958	in-del	-/C	0.00199481	0.0315187	intron-variant	ATG16L2	GRCh38.p7	11:72825745	CCAGGTGACCCTCTT[-/C]TAGCATCACTTGAGC	89849
rs548398323	snp	A/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836703	GGGCCTTTTGGAAAG[A/G]TCTGTTTACCCAAAC	89849
rs548428200	snp	G/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824184	CCCCAGCCCAGGCTT[G/T]GTCTGTGTCTGTGCC	89849
rs548473298	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72816460	CAGCGGGCAGTACCC[C/T]GCAGTGGTCATCCTT	89849
rs548569590	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839139	ACTAAGATCCTAGCA[C/T]ATCCTCCAAAGCAAA	89849
rs548601392	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72818782	AAAGTACGGGGAGTG[C/T]AACAATAAACAAGAC	89849
rs548699072	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814461	ATGGCGGGGCCGGGC[G/T]TCCCCGGTGCCCCCG	89849
rs548781965	snp	G/T			intron-variant	ATG16L2	GRCh38.p7	11:72834250	CGAAGATTCAGAGCA[G/T]CTGGATTTCATCCTA	89849
rs548840304	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72830579	GGTTTAAGCAATCCT[C/T]CCACCTGGTCTTCCC	89849
rs548925941	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827704	AGCTGTTTGGGAGGC[C/T]GAGGCGGGCAGATCA	89849
rs548973197	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815139	TGCTGGTGGATGCTG[A/G]CTGAGCCCAGCGAAG	89849
rs548991114	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822690	GACACCTGCAGAGGA[C/T]CGTGTGGTCGTAGGA	89849
rs548992201	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834073	ATTTGGTTCTTGGCA[C/G]ATCAAGCAGTAACAA	89849
rs549243569	snp	A/G	1.64991e-05	0.00287215	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843184	GGCTGCCTGAAACGA[A/G]TTCTGCTTCCGTGGA	89849
rs549322641	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830463	CCATCCAATCCTTTC[C/T]CTTACTATGGCCAGA	89849
rs549499520	snp	C/T	3.39018e-05	0.004117	intron-variant	ATG16L2	GRCh38.p7	11:72825261	ACTCACAGAGACATG[C/T]GCGGGGAGGGCCGGG	89849
rs549552442	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72816600	AGGGCAGAGGCCAGC[C/G]TGCCAGAAGCTTCCC	89849
rs549714613	snp	A/G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813219	CACTGACCTGGGGGC[A/G/T]TCTAGGCCTTCACTG	89849
rs549989403	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840635	TCTAAATCACTTTCA[A/T]AGCCATCATCTTGCA	89849
rs550017168	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813861	CTCCCTCTGGCCAAC[C/T]CCTATTTCATCCCTC	89849
rs550064861	snp	G/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838126	CCTCCATATTAGCTC[G/T]GCTAATTCTAAATGA	89849
rs550243229	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821128	GGTAGGTGGCTTGTG[C/G]CCAAATCTCTTAGCT	89849
rs550343669	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821026	GTGCTTGGGCAGGCC[C/T]GGGTTGGGTGAGGCC	89849
rs550346616	snp	C/T	0.00279162	0.0372561	intron-variant	ATG16L2	GRCh38.p7	11:72831975	CCCTGCCTGCTACCA[C/T]GGGGGTAGAGGTGTG	89849
rs550360576	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72826002	TGCCAGCAGTTAGGG[A/G]AGGTGTAGTCTCCAG	89849
rs550371971	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72820287	TTGTCATTTTATCAC[A/G]TGTAGATTTGTGTAA	89849
rs550421908	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72826389	CCTCCTCCTTGGGCC[A/G]GAGGCTCCTTTGCCT	89849
rs550505494	in-del	-/CTAA			intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827616	TTTAAACCAAAGACC[-/CTAA]CTAACTTTGGGCTTG	89849
rs550522976	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823233	TCAGGCTTCTGAATA[A/G]CTGTCACCAGGAGAG	89849
rs550849396	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838286	GTCTGGGGACTAACC[C/T]TGGGGAGGAGCCAGC	89849
rs550885266	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823480	TCCTCCATCCTTCTT[G/T]ATTTGCCTGTCATTG	89849
rs550910665	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72829678	TCATGGTACAGAGAC[C/T]TTTGGGCTAGTGGGC	89849
rs550948252	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817345	GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCT	89849
rs550982066	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814052	GCGACGGCCTGGGAA[G/T]CACCAGCGGCTCTCG	89849
rs551040655	snp	G/T	3.36672e-05	0.00410274	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838802	ATCATCACACCAGTG[G/T]GATTTCCACATCTTC	89849
rs551046830	snp	A/G	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72820037	GGCGTGAGCCACGGC[A/G]CCCGGCCTTTTCTTT	89849
rs551248230	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841400	CCCTTCAGGCGAATA[C/T]GTAGGTTTCTGAAGT	89849
rs551307815	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832970	CTCTTCTGCAGAGCT[A/G]TTCTGTAGGCATGAG	89849
rs551319989	snp	C/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72833685	CAGCACTTTTGGAGG[C/G]TGGGGCAGGTGGATC	89849
rs551420514	snp	A/C	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72830635	GCACCATGCTCGGCC[A/C]AACAGGGTGACTTTC	89849
rs551477176	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827945	AAAACAAAAACAAAA[A/C]CAAAACCAAAAACAA	89849
rs551505114	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827027	ACCTCAGGCTGTGGG[C/T]AGGAAAAAGACGTGG	89849
rs551615367	snp	C/G	0.00169566	0.0290681	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822019	GGAAGCTTGGGACCC[C/G]CTATCCGCTCTTTCC	89849
rs551883637	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827630	CCCTAACTTTGGGCT[C/T]GAATTGTTTGTAAAA	89849
rs551946729	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822634	CGACTGTACTTGTGC[A/T]CAGCCCCGTCCTGAG	89849
rs552011029	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72816112	GCCTCCCGAGTAGCT[A/G]GGACTACAGGCGCCT	89849
rs552101552	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72820635	GACTCACTCACATAG[C/T]GCGTCATGTCAGTGC	89849
rs552242683	snp	C/G			upstream-variant-2KB, splice-donor-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812632	CAATATGGCTCCTTA[C/G]CTGAGAGAAACGGCA	89849
rs552356250	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72818035	GAGTGCCCTGGGCAG[C/T]CCAGGATGAAGTGGG	89849
rs552601959	snp	G/T	0.00597247	0.0543191	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813066	TTCTCCTGGAGGAGG[G/T]GATGCATGATTAGGA	89849
rs552637011	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825787	AGGTAAGAGACAAGT[A/G]TGAACTGTTGGCCTT	89849
rs552680328	in-del	-/AAA	0.00318978	0.0398085	intron-variant	ATG16L2	GRCh38.p7	11:72819408	TGACATATTTTAATT[-/AAA]AAAAAAGAAAGATCT	89849
rs552732026	in-del	-/TTCA	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72818310	TCTCTTGGCTTCTCT[-/TTCA]TTCACCATGCTCTCC	89849
rs552768830	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840568	ATTAAATGCTTACTG[A/C]AAAAAGTGTTTCACA	89849
rs552814779	snp	C/T	3.32265e-05	0.0040758	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72825391	CCGCCTGATCCACCT[C/T]TGGAATGTTGTGGGA	89849
rs552826510	snp	C/T	0.000265654	0.011522	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822392	GAGGGGGGCAGCAGC[C/T]GCCCCCTGGAGGAAG	89849
rs552890183	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822792	GTATCCTGTGCTGGG[A/G]TCGGGAGGGGCTGGC	89849
rs553090628	snp	C/T			intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72814769	CGAGCCCCTCCTGGT[C/T]CCCCTGCCCTCGTCG	89849
rs553093577	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842534	GTAAGGCAGAGACTG[C/T]AGCCCACTTTTGTGT	89849
rs553100451	snp	A/G	9.88908e-05	0.00703105	missense, utr-variant-3-prime, intron-variant	ATG16L2	GRCh38.p7	11:72827226	TCCTACTGTAATGAC[A/G]TGGTGTGTGGGGACC	89849
rs553123167	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72835905	AGGCATGAGCTACCA[C/T]GCCCAGCCAATTTTG	89849
rs553241964	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836716	AGGTCTGTTTACCCA[A/C]ACCTTTCTATATTAA	89849
rs553301454	snp	C/T			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813121	GTTCCAAACATCAGG[C/T]TCGGCCTGTGCAAAG	89849
rs553304939	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72819005	CTGACCCCCACACCA[C/T]CCCCAGCCTCTGGGC	89849
rs553480281	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72830258	GACGGTGTTGGTTAA[A/G]TGGCAACACCTACAC	89849
rs553510780	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72812610	AAGGATTAGGAAACC[C/G]CTGCCCCAATATGGC	89849
rs553751386	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72832441	GGCCAAGGAGTTCCC[A/G]GGAATGAGGTAGGCA	89849
rs553776554	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823872	CATTACCAAATCCAT[C/T]GCTGCCCCGACCTTC	89849
rs553787405	snp	A/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831439	GAACCCAGGAGGAGG[A/T]GGTTGCAGTGAGCTG	89849
rs553822620	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72828606	CCCTCCCTGGAGGCC[C/T]CTCCAGACCAGGTCC	89849
rs554025893	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814086	TCGGCCCGGGCGCGG[C/T]GGGGTTAAGACACCC	89849
rs554054993	in-del	-/AAC	0.00279162	0.0372561	intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72827974	AAAACAAAACAAAAA[-/AAC]AAAGCTAGAGCCAGT	89849
rs554104790	snp	A/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832153	GCGCCATTGCGTTTC[A/T]CCCTCATTTCACAGG	89849
rs554174965	snp	C/G	0.00159617	0.0282053	intron-variant	ATG16L2	GRCh38.p7	11:72825551	CTAGACAATGCCTTG[C/G]AAAGAGTGAGACTCT	89849
rs554219260	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72826057	CGATTCTGTCTTCTA[A/G]CCTGGGGATGTGTCG	89849
rs554287127	snp	G/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72819871	CTGCCTCAGCCTCCC[G/T]AGTAGCTGGGACTAC	89849
rs554515981	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72828664	GAGGAAGCTCTGGAA[A/G]CTCACTGCAGAGGGC	89849
rs554558413	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841074	TTGGGATACTGAGGC[A/G]GGAGGATTACTTGAG	89849
rs554680370	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823018	CCACCCCAGAGGCTG[C/T]CAGGGTCTTCCTCTT	89849
rs554682364	snp	C/T	1.64838e-05	0.00287083	synonymous-codon, nc-transcript-variant	ATG16L2	GRCh38.p7	11:72828470	CAACACACTCAAGGT[C/T]ATCGACCTGCGTGTC	89849
rs554734887	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72836039	AGGCATGAGCCACTG[C/T]GCCCGGCTGAACACA	89849
rs554765755	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838369	AATTCTCAATCAGAT[A/G]AGCAAAAGCCACTTG	89849
rs554767261	snp	C/G			upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813480	CATCTAGCTAGAGAC[C/G]GTTTGACCACAGTTC	89849
rs554819732	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72824619	TGCTCCTTGGGGCCA[C/T]GTTCTGCCGCCTGCC	89849
rs554883122	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72824935	TGGTCCCAAGAGGCC[A/G]GGGAAGCAAGGCTGG	89849
rs554945292	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72823201	CTTCTTGGGATCAGA[A/G]CTCTGGGGGTGGGGA	89849
rs555046643	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72832322	TGCCATCGGGTGGAG[C/T]TGCCTCTCTCAGGGA	89849
rs555089251	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72833266	CAGACGTGGACCCAT[C/T]TGTGAGATTCAGACA	89849
rs555290760	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827081	AAGACCTGGGTTCTA[A/G]TCTTGGGAGGACACT	89849
rs555303244	snp	C/G	0.00162614	0.0284679	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822380	GTGTCTGGAAGGGAG[C/G]GGGGCAGCAGCCGCC	89849
rs555444484	snp	C/T	0.000400105	0.0141383	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841471	TTTGCTGAAGGAGAC[C/T]GGGGAAAGTACAGGG	89849
rs555482434	snp	A/G			intron-variant	ATG16L2	GRCh38.p7	11:72825207	CCACGTCTGCAGCAG[A/G]CTGTGTCTGCACAGG	89849
rs555503496	snp	C/T	0.000798403	0.0199641	intron-variant	ATG16L2	GRCh38.p7	11:72833000	GGACCATGGCCTCTG[C/T]CTGCCCTGCCCAATC	89849
rs555597861	in-del	-/GGGTGCGCGGCCA	0.0123036	0.0774623	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814019	TCTGGGTCCCTGGCT[-/GGGTGCGCGGCCA]GGAGCGCGACGGCCT	89849
rs555714802	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843003	ACTTTAGGGTTCTAC[C/T]GTGCAGGACAAACGT	89849
rs555757256	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ATG16L2, LOC107984421	GRCh38.p7	11:72815587	AATCAGACTGAAGGG[C/T]CAGTCTTGAAACCTT	89849
rs555774159	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834580	GAGATAACCTCATTC[C/T]ATTCCTTTTTTTTTT	89849
rs555968159	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72830357	TGACCCGTTCCTCCT[A/G]CACCCCATGTCCCTG	89849
rs556004301	snp	C/G			intron-variant, downstream-variant-500B	ATG16L2	GRCh38.p7	11:72828222	ATGAGTCACTCGCAG[C/G]CTTTACCCCAGCGAT	89849
rs556025889	snp	C/T	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72835638	GAGTGTAAATGGATA[C/T]AGTCCTTATAGGAAG	89849
rs556085468	snp	A/C	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72817562	GCCAAGGCCTAGGGG[A/C]ATCTTAGAGCAGAGG	89849
rs556194744	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839243	CAAAAGAGAAGGCTA[G/T]AAAGGTAGGCTAGGG	89849
rs556335296	snp	C/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836342	GGCATCCAGAATGCC[C/G]GCTTCCTGGAAGCCA	89849
rs556413217	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838539	ATGAGGGCTGCCCCC[C/T]TCTTTGCTCCTAGGG	89849
rs556494286	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72813466	AGCTGGCTCTCTAGC[A/C]TCTAGCTAGAGACGG	89849
rs556681352	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72825182	GACAGAGAAACTGGG[A/G]AGGGAGATACCACGT	89849
rs556744605	snp	C/G	0.00119737	0.0244387	intron-variant	ATG16L2	GRCh38.p7	11:72825516	GTGTTTCTCTATCTG[C/G]AATATTCTGTGGGCA	89849
rs556820688	in-del	-/TG			intron-variant	ATG16L2	GRCh38.p7	11:72818834	TCCTCTGAAAGAGAC[-/TG]TGATAGCCCAGGAAA	89849
rs556826875	snp	C/G	0.00012216	0.00781441	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72822434	AGCCCCGCCTGCGTG[C/G]GAGGCGCCGCGCCAG	89849
rs556842505	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	ATG16L2, LOC107984421	GRCh38.p7	11:72814073	GCGGCTCTCGAACTC[G/T]GCCCGGGCGCGGCGG	89849
rs556971473	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72834278	CTAAGGCCACTGGGA[A/G]AGGGCTGGGCAGTCA	89849
rs556997980	snp	G/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	ATG16L2	GRCh38.p7	11:72821794	CTCAGGGAGGCCCGG[G/T]GCCAACTATACGGGA	89849
rs557046230	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836823	TGTAAAGAAAGCACA[A/T]CTGCACAGAGGCTCC	89849
rs557075251	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72835441	GTGGTGGTGAGGAGA[A/G]GTGGTGGTGAGAAGA	89849
rs557078109	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ATG16L2	GRCh38.p7	11:72822967	GGCCCTTCAGGTGAG[G/T]ACCCAGGTGACAGTC	89849
rs557079282	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	ATG16L2	GRCh38.p7	11:72827450	GTGCCTCTCGGCTGG[A/G]CTCAGCTCCCGCAGG	89849
rs557107292	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837754	GGTTCTTCCTTCCAC[A/G]GAAATGTCAGGGTAG	89849
rs557500352	snp	A/G	0.000399281	0.0141238	intron-variant	ATG16L2	GRCh38.p7	11:72831518	CTCAACAACAACAAA[A/G]TTCTCTTATTCAAGG	89849
rs557560712	snp	C/T			intron-variant	ATG16L2	GRCh38.p7	11:72834772	ATTTTTAGTAAGAGA[C/T]GGGGTTTCCATTATG	89849

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