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

FCHSD2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs76555174	snp	C/T	0.0169612	0.0905146	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902561	ATCACTGTCACAAGG[C/T]TGGAACTGGAAGGGC	9873
rs76569812	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73047554	CACTGCCAAGGATAA[C/T]GCAAAAAGAAATCCT	9873
rs76579313	snp	A/G	0.0185938	0.0946107	intron-variant	FCHSD2	GRCh38.p7	11:72903610	TCATTGCATTTACAT[A/G]CCTTGGGAAAGAGTG	9873
rs76581108	snp	A/T	0.0444908	0.142359	intron-variant	FCHSD2	GRCh38.p7	11:72954155	ATGCAAAGATAATAA[A/T]GGTGGCTTAGATTAT	9873
rs76608021	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73046005	TTTTTTTTTTTTTTT[A/T]TTAGAGACAGGGTCT	9873
rs76615529	snp	A/C	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73039194	GTAAGCAATTCCTTT[A/C]GGATTCCTCATAAAC	9873
rs76640911	snp	A/G	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73130273	TTTCTTAGAGATAGG[A/G]TCTTGCTAAGTTGCC	9873
rs76641528	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72936751	TGTATTTTTAACTCC[A/G]GAATTTATATTTGAT	9873
rs76645433	snp	A/C	0.0372196	0.131242	intron-variant	FCHSD2	GRCh38.p7	11:73000744	AATTATGCCGAAAAG[A/C]GGTATTACTAAAAAG	9873
rs76654236	snp	C/T	0.0228947	0.104514	intron-variant	FCHSD2	GRCh38.p7	11:72966897	CTGGGATGTGAACCC[C/T]GATTATGAGTTAAGA	9873
rs76727972	snp	C/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72867701	CTCTCTTTCACTTCC[C/T]GCAATAATTTTAAAT	9873
rs76735116	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73038349	CCTGTCTCTTTAAGA[A/G]AAAAAAAAAAAAAGG	9873
rs76749858	snp	C/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73028124	ACTGCCTACTGGAGG[C/G]GTGAGAAGAGAGCCA	9873
rs76757350	snp	A/G	0.0244538	0.107838	intron-variant	FCHSD2	GRCh38.p7	11:73101742	GCACCCCCCGCCCCC[A/G]AAAAAAACACAACAC	9873
rs76760498	snp	A/G	0.0410537	0.137264	intron-variant	FCHSD2	GRCh38.p7	11:72884456	AGGTAATATAAATTT[A/G]GAAATAATGTGATTA	9873
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	9873
rs76790176	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72991535	AGTGGGCTTCATCCC[C/T]GGGATGCAAGGCTGG	9873
rs76793740	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72882369	TCTCAAAAAAAAAAA[A/G]GTACAGAGTAGAATG	9873
rs76793820	snp	A/G	0.235564	0.249583	intron-variant	FCHSD2	GRCh38.p7	11:72908815	ATGCCACTATGCCCC[A/G]CTATAGTTTTGTACT	9873
rs76815220	in-del	-/T	0.0955749	0.196603	intron-variant	FCHSD2	GRCh38.p7	11:72957020	CAAAGGACTCTAGTC[-/T]TTTTTTTTTTTTCTT	9873
rs76821975	snp	A/C	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72951893	GTCCTTACTCCCATA[A/C]AACTTAGGGAAAATC	9873
rs76849542	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72963929	GTGTCATGAATAGAT[C/T]TCACAGTTGAATAAC	9873
rs76871630	snp	G/T	0.5	0	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143611	TTTTTTTTTTTTTTT[G/T]GAGTCACGGGGCTGT	9873
rs76873900	snp	C/G	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73006911	TGAAACCAAATGTGT[C/G]TGGCTCCCAAACCTC	9873
rs76904120	snp	A/G	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73020033	TGATGCATAATGCTG[A/G]TTTGATTTGCAATTC	9873
rs76916550	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72870342	GCTCCTTTAAGACTC[A/G]AGCATTGACATTCAG	9873
rs76936742	snp	C/T	0.0471551	0.14613	intron-variant	FCHSD2	GRCh38.p7	11:73114876	AAGCTACAAGCTGTG[C/T]GCCCAAAACTGAGGG	9873
rs76941532	snp	A/G	0.0329836	0.124112	intron-variant	FCHSD2	GRCh38.p7	11:72869302	AAGTTCTTCCTAATC[A/G]ATTAATTACAACAAT	9873
rs76949292	snp	C/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72865367	CTTTATTTATATTAT[C/T]AGATCTTCCACAAAA	9873
rs76951135	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72914979	TTTTTTTTTTTTTTT[G/T]TTTTGCAAACTAAGC	9873
rs76953154	snp	G/T	0.0418186	0.138422	intron-variant	FCHSD2	GRCh38.p7	11:72851217	TTGAAAAAACAACCT[G/T]TTCACTGAAATTAAA	9873
rs76967156	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73108206	TGTCAATGACTTCTT[C/T]TGAAAAATGTCCACT	9873
rs76982282	snp	C/T	0.0414363	0.137845	intron-variant	FCHSD2	GRCh38.p7	11:73057335	ACAGAAGCTAAAGAA[C/T]CACAAGGAAGAAAAA	9873
rs77004023	snp	C/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73011061	AGTGGCAGGGGTGGG[C/T]AGAACCAACCTCAGG	9873
rs77006715	snp	C/G	0.030278	0.119257	intron-variant	FCHSD2	GRCh38.p7	11:73098148	TAGGGTATAAAGCTA[C/G]GTTGTTAACTTGAAA	9873
rs77038197	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73091905	AATTAGCTGGTAGCG[C/T]GCACCTGTAATCCCA	9873
rs77041803	snp	C/T	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72936974	TCCCTGTGTATGGGC[C/T]ATATATTCCTGTTTC	9873
rs77066090	snp	C/T	0.0513262	0.151752	intron-variant	FCHSD2	GRCh38.p7	11:72999735	TATTCTGATATTGAG[C/T]AAGGTGGCAGTAATT	9873
rs77146803	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72861931	AGCGAAACGCCGTCT[A/C]AAAAAAAAAAAAAAA	9873
rs77154202	snp	G/T	0.145642	0.227177	intron-variant	FCHSD2	GRCh38.p7	11:73103535	TGTCTTATTGCTAAC[G/T]ATATTACATTGAATA	9873
rs77175480	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72871057	AAAAGTTCCTATTCT[C/T]CAAATTCAAGAAAGG	9873
rs77175727	snp	G/T	0.0126467	0.0785075	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73000992	ATAAAAACAATACCC[G/T]TTTTAGTTGCTGTTC	9873
rs77188826	snp	C/T	0.0704125	0.17392	intron-variant	FCHSD2	GRCh38.p7	11:72914309	TGTGAGTCAGGTGCC[C/T]AGCCTGCCCTAAGCA	9873
rs77193680	snp	C/G	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73023135	TCTCCTTGACCTTTG[C/G]TGAAAAGTTTTAACA	9873
rs77203641	snp	A/G	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73109729	GCTAGGACTTCCAGT[A/G]ATACACTGAGTAACA	9873
rs77204389	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72966202	TCTCACTCTGTCGCC[A/C]AGGAAGGAGTGCAGT	9873
rs77217967	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73127495	AAAAGCCAAGAACAC[A/G]AGCCAGACTTACAAA	9873
rs77230680	snp	C/T	0.0441612	0.141882	intron-variant	FCHSD2	GRCh38.p7	11:72897374	ACATGTACAGACTTT[C/T]TTTCTTTGTCTTATT	9873
rs77247067	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72924652	GGAAGTCTTCCATTG[G/T]ATCTTATGTTTGGCT	9873
rs77254773	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73044272	TCAATTAAAAAAAAA[C/T]TTATGAATATTTCCA	9873
rs77263609	snp	A/G	0.0425829	0.139564	intron-variant	FCHSD2	GRCh38.p7	11:73046174	TTTTTAATGTTTTGT[A/G]AAGACAGGGGTCTTG	9873
rs77310163	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72880881	TCGAAAAAAAAAAAA[A/G]GAAAACAACAACAAC	9873
rs77315987	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73095911	GACTGGCTGAGGATT[A/T]AAAAAAAAAAAAGTT	9873
rs77322995	snp	G/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72974937	TTAGGTGAATCAGAG[G/T]TACAAGAGCTAGAGA	9873
rs77340504	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72896788	AAAAAAAAAAAAAAA[A/G]AAGAAAGAAATATGC	9873
rs77351594	snp	A/G	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:72924085	TTCACTTTCTTGAAA[A/G]TTTCTTTTGATGTAC	9873
rs77360270	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965437	TTCTACCAGGTGAGA[A/C]AAAATAAGTCTTAAC	9873
rs77363202	snp	C/G	0.0418186	0.138422	intron-variant	FCHSD2	GRCh38.p7	11:73134546	TGGGAATCTACAGTT[C/G]AGAGAAAGTAACATA	9873
rs77363286	snp	C/T	0.0494327	0.149241	intron-variant	FCHSD2	GRCh38.p7	11:72935887	TTTTTCTATAAAGCT[C/T]GTGTTATCCTCTTGC	9873
rs77393561	snp	C/T	0.0637235	0.166737	intron-variant	FCHSD2	GRCh38.p7	11:73038420	TATAATTTATCCAGT[C/T]GAATCCTCTCAGATC	9873
rs77393660	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73066714	GAAGACATTTATGTA[A/G]CCAACAGACATGAAA	9873
rs77396132	snp	C/T	0.0433465	0.140692	intron-variant	FCHSD2	GRCh38.p7	11:73076249	TTAGGCAGCATTATA[C/T]CTAATAACCAAATTT	9873
rs77403018	snp	A/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:72895643	GAGAAAGGTGACTAA[A/T]CCAGTAGAGGGCCTA	9873
rs77424910	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73048183	CCCAAAGCATTTGAG[G/T]CATAGCTAGAGCAGC	9873
rs77429641	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73136416	AACACAAAAATTAGC[C/T]GCGCACCTGGAGTCT	9873
rs77447505	snp	A/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72846026	TAATATCTTCCTCAT[A/G]GGGTTATTGAAGGGA	9873
rs77487804	snp	G/T	0.0648419	0.167978	intron-variant	FCHSD2	GRCh38.p7	11:73035150	TTTTAGTTTTTATTT[G/T]TATGTATGTATGTAT	9873
rs77502656	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72934330	CTATGAAGAGCCATG[C/T]CTTTTTTTTTTTTTT	9873
rs77512961	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73106405	AATGAGACTCTGTCT[A/C]CAAAAAAAAAAAAAA	9873
rs77557631	snp	A/C	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72898343	CTATATCTTACGTAA[A/C]TTTAGATAAAATATT	9873
rs77570823	snp	G/T	0.0444908	0.142359	intron-variant	FCHSD2	GRCh38.p7	11:73069520	TCACTAACAAAGCAA[G/T]GGATAAGATAAAACC	9873
rs77576882	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72941978	TATGATCAAATACTA[C/T]GCAGTCATTAAAATC	9873
rs77605839	snp	A/G	0.00831782	0.0639509	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72868021	TTCAGCTTTCAATTT[A/G]ATTATCTAGAGAACC	9873
rs77639079	snp	C/T	0.226188	0.248863	intron-variant	FCHSD2	GRCh38.p7	11:72899361	TTTTACCAAAGAAGA[C/T]ATATGAGTGGCTAAT	9873
rs77656109	snp	G/T	0.0252325	0.109451	intron-variant	FCHSD2	GRCh38.p7	11:72858134	GAGAATCCAGATAAA[G/T]AATCTGGTAATACCT	9873
rs77663794	snp	A/G	0.0901694	0.192235	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840002	AAACGAGGCAAATGT[A/G]GAGAAGCACATCAGC	9873
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	9873
rs77715619	snp	A/C	0.0418186	0.138422	intron-variant	FCHSD2	GRCh38.p7	11:73013200	CCAGTTAACCTCTAA[A/C]CCACATACTTCACAG	9873
rs77717172	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72887460	ATGCCACAATTAGCT[G/T]CCACCTTACCTCTGC	9873
rs77718624	snp	A/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73075006	GAGACTTTAACAGGC[A/T]CTTAATAACACAAAA	9873
rs77731311	snp	A/C	0.0919752	0.193722	intron-variant	FCHSD2	GRCh38.p7	11:72967707	GTGATGGTTGTACAA[A/C]CTAGTAAATATAATA	9873
rs77754605	snp	A/T	0.0337553	0.125452	intron-variant	FCHSD2	GRCh38.p7	11:73097388	TTTATTTATTTATTT[A/T]TTTTTTTTGCATCTC	9873
rs77757462	snp	C/T	0.0444908	0.142359	intron-variant	FCHSD2	GRCh38.p7	11:72848339	ACTCTCATCACACTC[C/T]GTCTCTATACCTGCT	9873
rs77780279	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73063720	CTCTTCTTGTTGAAT[C/T]GATCCCTTTACCAAT	9873
rs77781108	snp	A/G	0.031825	0.122064	intron-variant	FCHSD2	GRCh38.p7	11:73125136	ACCAGAAATGCTGAA[A/G]GAAGTTCCTTAAGCT	9873
rs77786657	snp	C/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72980977	TAATTCAGAAAAATA[C/G]ATATTTCCTTAACAT	9873
rs77796017	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72861936	AACGCCGTCTCAAAA[A/C]AAAAAAAAAAAAAGA	9873
rs77800942	snp	C/G	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72985571	AAGACTCTAACAATA[C/G]GCTCTATGAAGTCCT	9873
rs77809521	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73111464	TATCTTTCTCCATCC[C/T]TTTTTTTTTTTTCAG	9873
rs77836591	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72970656	AAAGTCCATCCCTGT[A/G]AAATGCCACTGTCTG	9873
rs77847109	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73009052	ATTTAAAAAAAAAAA[A/G]GGTCCAAGAGAAAGT	9873
rs77853902	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73130843	GCATGTTACCTTTTA[C/T]TAATTATAAAATCAG	9873
rs77884652	snp	A/C	0.138546	0.223781	intron-variant	FCHSD2	GRCh38.p7	11:72859704	AAATCTGCAGAGGGT[A/C]CTCCTCAAGACTTTG	9873
rs77894281	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72966166	CTTCTTTGAACTGAG[C/T]CTTTTTTTTTTTTCA	9873
rs77907627	snp	C/T	0.0532157	0.154195	intron-variant	FCHSD2	GRCh38.p7	11:72859131	AGCAGTCTCCCCTTA[C/T]GTGTGGTTTGGCTTT	9873
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	9873
rs77960535	snp	A/C	0.0422008	0.138995	intron-variant	FCHSD2	GRCh38.p7	11:73051176	TAAAAATTAGCAGGA[A/C]GTGGTGTCACACATG	9873
rs77963674	snp	A/C	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73010231	TCAATGAATTCTTCC[A/C]TTACAGAATTTCTGT	9873
rs77971648	snp	C/T	0.0414363	0.137845	intron-variant	FCHSD2	GRCh38.p7	11:72929435	TTCTGGTGGGTAAGA[C/T]AGCTGGAGGCCTTCT	9873
rs77981438	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73060244	TTTAAACAAATGTCT[A/G]ATTGTACCATATTTT	9873
rs77983294	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73084961	AGAGTAAGAAGGAGG[A/G]AAAAAAAAAAAAAAG	9873
rs77986964	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73091400	AAACAACAAAAAAAA[A/T]TAGCCAGGTGTGGTG	9873
rs78005959	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73119302	AGCGAGACTCTGCCT[A/C]AAAAAAAAAAAAAAG	9873
rs78059239	snp	C/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73040877	TCCCTTCAACCTTCC[C/T]ACAAACTGCTCCCCC	9873
rs78060984	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73094384	ATAATTAAACTTACA[C/T]TTATTTTGATATAAC	9873
rs78061964	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72923520	TTAGTGATTAGGAAC[A/G]GTATATCTTTGTAGT	9873
rs78063789	snp	A/T	0.0513262	0.151752	intron-variant	FCHSD2	GRCh38.p7	11:72876975	TAATATGATCACTTC[A/T]TTTTTTTTTTTTTTA	9873
rs78082263	snp	C/G	0.143959	0.226396	intron-variant	FCHSD2	GRCh38.p7	11:72875391	TTTATTTGACAGAGT[C/G]TCGCTCTGCTGCCCA	9873
rs78088433	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73046006	TTTTTTTTTTTTTTT[G/T]TAGAGACAGGGTCTC	9873
rs78103413	snp	A/G	0.0134861	0.0810011	intron-variant	FCHSD2	GRCh38.p7	11:73096424	GATGTGGTGGCGGGC[A/G]CCTGTAATTCCAGCT	9873
rs78104946	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:72885582	TAGGGTACCAGTCGG[C/T]GATACCATGCATGGG	9873
rs78106592	snp	A/G	0.0729998	0.176553	intron-variant	FCHSD2	GRCh38.p7	11:72936116	GGGAAGACACTGACC[A/G]TTCTTGAGCTTTCCA	9873
rs78113905	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946953	CCCTCTTTGTGGGAC[C/T]AGTCTTTGCAGCCAT	9873
rs78115530	snp	A/G	0.0425829	0.139564	intron-variant	FCHSD2	GRCh38.p7	11:72882976	ACAGACATATAGACC[A/G]ATGGAACTGAATAAA	9873
rs78124059	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72844906	GAAAAATAATATTGA[A/G]GAAAAAACCCCACTC	9873
rs78125524	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72982043	TATGGAAAATATATG[C/T]AGAGTTTTCATCTGA	9873
rs78139650	snp	C/T	0.0444908	0.142359	intron-variant	FCHSD2	GRCh38.p7	11:72870321	GCCTGTTTGATATAA[C/T]TGGGGGCTCCTTTAA	9873
rs78165696	snp	A/G	0.0452528	0.143452	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143759	ACTTCCCAGATGACC[A/G]CATGACCAGAAATTG	9873
rs78167218	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72850075	TTTTTTTTTTTTTTT[G/T]TTTTTGAGATGGAAT	9873
rs78186456	snp	A/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73060063	TTAAAAGCAGGTAGG[A/G]TACACTGCTATCAGA	9873
rs78195769	snp	A/G	0.0980852	0.198549	intron-variant	FCHSD2	GRCh38.p7	11:72996663	AGAAAATCTTTAAAA[A/G]AACATGAACTTTAAA	9873
rs78197229	snp	A/C/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73048276	CTCATGCCATGTACC[A/C/G]ACACACATATGGGAC	9873
rs78201152	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73065150	TGATTGTGGTGGATA[A/C]GCTTTTTGATGTGCT	9873
rs78216886	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72872352	AATTCAGTGGCTTAC[A/G]GTATATTCATAGTAC	9873
rs78217242	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72998189	TGGAATTATCTTGCT[A/G]GAAGATTTTTATATT	9873
rs78218814	snp	A/G	0.0425829	0.139564	intron-variant	FCHSD2	GRCh38.p7	11:73030921	TATCTCTATACTTGC[A/G]CGTCCTGAATTTCTG	9873
rs78242798	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73063672	TCTTTTTTTGATCTT[C/T]GTTGGTTTAAGGTCT	9873
rs78246085	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73034501	AATTCGGTACCAGAG[A/G]CTGAGCCTGTACCAA	9873
rs78281067	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73063799	ATAAAGCAACTTCTT[A/G]GAGACCTACAAAGAG	9873
rs78285898	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73070750	AATTAAAAAAAAAAA[A/G]GAAATTGAACAAGTT	9873
rs78295328	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72968092	CAAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAGA	9873
rs78329834	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73127196	ACACTTTTCATAACA[C/T]CAGAAATAACATTTT	9873
rs78338303	snp	A/G	0.046775	0.145601	intron-variant	FCHSD2	GRCh38.p7	11:73084557	CACCACATCTGGTTA[A/G]TTTTTAAATACTTCT	9873
rs78339540	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73109556	ACTGATTTCTGTATG[C/T]TAATTTCATATCCTG	9873
rs78345869	snp	C/G	0.0338708	0.126327	intron-variant	FCHSD2	GRCh38.p7	11:72982832	TAAATTCAGGATAAA[C/G]GTAATGAAATTTTTT	9873
rs78355612	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72952341	TATCTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA	9873
rs78373710	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72949222	GGGAGGCCCATGGCG[G/T]GCAGATCACCTGAGG	9873
rs78392861	snp	C/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73084884	GTTTAAAGACTTTAC[C/T]GTTATGTGCCAGGAA	9873
rs78394787	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73049686	ACTTAGAGTATAATA[A/T]AAAAAAAAAAAAAAA	9873
rs78400285	snp	G/T	0.0170251	0.090679	intron-variant	FCHSD2	GRCh38.p7	11:73051603	CGACTTTATACTATT[G/T]TACACAAAAGTATGA	9873
rs78420754	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73086245	AAAACTCCGTCTCTA[C/G]TAAAAATACAAAAAT	9873
rs78484827	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73017452	CAACTACCTGCTTGA[A/G]GCAAAAATTACTCAA	9873
rs78496443	snp	C/T	0.0422008	0.138995	intron-variant	FCHSD2	GRCh38.p7	11:72897691	CCCATGTTTTCTCCA[C/T]TGTACACCACCTGTA	9873
rs78519750	snp	A/G	0.0240643	0.107019	intron-variant	FCHSD2	GRCh38.p7	11:72953813	GAGTGAGGGAGTATC[A/G]AGTTCTGTGGCTCTC	9873
rs78560506	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73009054	TTAAAAAAAAAAAAG[G/T]TCCAAGAGAAAGTAG	9873
rs78560848	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73121657	TAATTGTTAAGGGCC[A/C]AAAAAAAAAAAAGTC	9873
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	9873
rs78601302	snp	C/G	0.0221141	0.102801	intron-variant	FCHSD2	GRCh38.p7	11:73048804	CTCAAGAGAAAGGGT[C/G]GGGAATGAATATTTG	9873
rs78632327	snp	C/T	0.0486741	0.148216	intron-variant	FCHSD2	GRCh38.p7	11:73084879	CCTGAGTTTAAAGAC[C/T]TTACCGTTATGTGCC	9873
rs78642949	snp	C/T	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72957760	GAGGCATTATGTTCA[C/T]GATTTGCTCTCAAAT	9873
rs78654834	snp	A/G	0.0221141	0.102801	intron-variant	FCHSD2	GRCh38.p7	11:73056378	CTGCTAGGGAATACC[A/G]GTATTAGTAAAGAAC	9873
rs78659915	snp	C/T	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72939027	CAGGATATTTTCAAA[C/T]TTTAATACAGTAGCC	9873
rs78680390	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73047247	CTACCATTTTTTTTT[A/T]AATTAAAGAAAAAGA	9873
rs78691374	snp	C/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72912939	GTTTAATTGACCCAT[C/G]GTTCTGCAGGCTGTA	9873
rs78691864	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72893749	GGAGACTCTGTCTCC[A/C]AAAAAAAAAAAAACT	9873
rs78693033	snp	A/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72924699	TTTTTTTTTTTTTAA[A/T]TACACAAATTCTGTC	9873
rs78715889	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72968090	AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	9873
rs78724679	snp	C/T	0.0170251	0.090679	intron-variant	FCHSD2	GRCh38.p7	11:73020594	ACTTTAAAAGTAATA[C/T]AGAATTTCACTCCCA	9873
rs78753085	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72895031	CACATATTTCAAATA[C/T]GCCACACACCTTGAA	9873
rs78766352	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72875499	CCACCACATCTAATG[C/T]TAAAGTTTTTTGTAG	9873
rs78782831	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73054382	CAGACAGGGGGCTAG[A/G]AAAAAAAAAGAAATT	9873
rs78807111	snp	C/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:72911552	TTGAAAGAGACTGCA[C/T]TGAATCTGTAGACTG	9873
rs78835923	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73121662	GTTAAGGGCCAAAAA[A/G]AAAAAAAGTCTACAT	9873
rs78838741	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72933234	CTTAAATTAGGTCAT[A/C]CCTGGGATAGAGGCT	9873
rs78849193	snp	C/T	0.0532157	0.154195	intron-variant	FCHSD2	GRCh38.p7	11:72855989	GTTTCTTGCCCGCTA[C/T]ACCCAAGCACTTATT	9873
rs78852731	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72980696	ATATATATATATATA[A/T]AATGTATGTATGTAT	9873
rs78856007	snp	C/T	0.0298908	0.118541	intron-variant	FCHSD2	GRCh38.p7	11:72855905	TACTCTTTGAACTAT[C/T]AGAATATGCACGTTT	9873
rs78861246	snp	C/G	0.142609	0.225759	intron-variant	FCHSD2	GRCh38.p7	11:72978687	GATGGTTTAAAAGTG[C/G]CACTTCCCCCTTCGC	9873
rs78873590	snp	C/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73051849	ATAATAGACCTTCAG[C/G]ATGCTAACACGGTAT	9873
rs78888296	snp	C/T	0.0267878	0.112589	intron-variant	FCHSD2	GRCh38.p7	11:72875575	CTCAAACGATCCTTC[C/T]GCCCTCCTGCCCTGG	9873
rs78927304	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73039530	TCCAAAAAAAAAAAG[A/G]AAGAAAGAAAAGAAA	9873
rs78982391	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72876142	GCAGCCTGGGCAAAA[C/T]AGCAAGACCCTATCT	9873
rs78984730	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72980551	TGGTTAGGATAATGC[C/T]AAGGCAATATTAAGC	9873
rs79059902	snp	C/G	0.46875	0.121031	intron-variant	FCHSD2	GRCh38.p7	11:73065169	CCACCACGATCAAGT[C/G]AGCTTCATCCCTGGG	9873
rs79063774	snp	A/G	0.0189856	0.0955633	intron-variant	FCHSD2	GRCh38.p7	11:73000237	AAAATATTATTTCCC[A/G]AAATAATTACTTTAA	9873
rs79069192	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72850662	CTGGCCAGGACAGAG[A/T]TTTTTTTTAAATCAA	9873
rs79070889	snp	G/T	0.375	0.216506	intron-variant	FCHSD2	GRCh38.p7	11:73063777	TTGCTTTATGAATCT[G/T]GGTGCTCCTGTATTG	9873
rs79078438	snp	C/T	0.0165278	0.0893908	intron-variant	FCHSD2	GRCh38.p7	11:73097296	TGCAGGCGTGTAATC[C/T]CACTTGGTCGTGGTG	9873
rs79094432	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72921355	ACTTTTAAATGAAAC[A/G]ACTGCTGTCAAAGAA	9873
rs79117587	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72871343	AAACCCTATATATCA[A/G]CTCTTGCTTTGTTCA	9873
rs79158392	snp	C/T	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:73002046	TGAAATTCTGATAGA[C/T]TATAATATTCATCTC	9873
rs79181259	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72938798	AAACTATTGAAAAAA[A/T]TCTTATCAAGCTAAC	9873
rs79183144	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73002575	AACTATTAATTTATA[C/T]TTAAAATACATTTTA	9873
rs79185012	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73033289	CGAGATTCCGACTCA[A/C]AAAAAAAAAAAAAGT	9873
rs79208044	snp	A/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73057803	ACAGCTATACAGGGA[A/T]TGAGTTCCCCTCAGT	9873
rs79214015	snp	C/T	0.0391387	0.134304	intron-variant	FCHSD2	GRCh38.p7	11:72912710	TTGGTATTAGTTATT[C/T]TTTAAATGTTTGATA	9873
rs79227805	snp	C/T	0.0711525	0.174681	intron-variant	FCHSD2	GRCh38.p7	11:73010314	TGTTTTTCTGATTTC[C/T]CTGTACTGTTTTTCA	9873
rs79256301	snp	C/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73022177	TACTTTTAATGGTGA[C/G]TGAATGCTTTTCCCT	9873
rs79257384	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73124755	AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAGG	9873
rs79280809	snp	A/T	0.0520825	0.152737	intron-variant	FCHSD2	GRCh38.p7	11:72889479	GAAAGTACAGAAAAA[A/T]CACATATAATGCTTG	9873
rs79297540	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73116929	ATTATATTTTTTCAT[A/G]TAAAACCTTTCCATT	9873
rs79305492	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72848815	CGTTCAAGTAAATAT[A/T]ATGGGAGGTGGTATC	9873
rs79329636	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72955102	CCTGGAGAGCGTCAG[A/G]TCTCACAGACTGCTA	9873
rs79336645	snp	A/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72961010	GGGTAAATAGAAAAT[A/G]GTGACCTAGGAATGG	9873
rs79339967	snp	C/T	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73077818	CAGATGTGTTCATTA[C/T]CTTGCTTGTGATGCT	9873
rs79351640	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72959671	AATAAATTGCTAAGA[C/T]AGACATTTCAACGCA	9873
rs79378475	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73052014	TTTCCAATGACACCA[C/T]AGTCTGATGAATTCA	9873
rs79426191	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73090913	AGACCCATTAAGTAA[C/T]CACGCTTCATTCCCC	9873
rs79429231	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73080318	AAAAAAAAAAAAAAA[A/G]AGAAAGAAAGAAAAG	9873
rs79443180	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73063775	CCCAGTACAGGAGCA[A/C]CCAGATTCATAAAGC	9873
rs79469405	snp	C/T	0.0425829	0.139564	intron-variant	FCHSD2	GRCh38.p7	11:73029493	TCCCTGGCCCATTGG[C/T]AGGCAGCCATGCATA	9873
rs79483878	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73072619	ACAGAAAATAATACT[C/T]AATTTTGCCCTGGTG	9873
rs79504019	snp	A/G	0.0260105	0.111035	intron-variant	FCHSD2	GRCh38.p7	11:72887189	CCATTAATCTCTGTG[A/G]TTTATTATGTACCTT	9873
rs79569799	snp	A/G	0.0422008	0.138995	intron-variant	FCHSD2	GRCh38.p7	11:73013756	AATTAGGGTTTATAA[A/G]CTAGCCTAGGAGCAT	9873
rs79596649	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72850663	TGGCCAGGACAGAGA[A/T]TTTTTTTAAATCAAG	9873
rs79611522	snp	A/T	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72977425	GTAAAAAATATTTGT[A/T]AATTATCCAGTTGAC	9873
rs79634977	snp	A/C	0.0283406	0.115616	intron-variant	FCHSD2	GRCh38.p7	11:72961634	GTGACTTGAAGACAG[A/C]AATTCCCTACCCTGT	9873
rs79638730	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72913832	AAAAACCCAAAAAAA[A/C]AACAAAAAAAAAAAC	9873
rs79661690	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73093619	ATTTCTTTTTTTTTT[G/T]AGACCGAGTTTCGCT	9873
rs79668918	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73047951	TAAGTAATTTATGTA[C/G]AGTGATTATGTTAAC	9873
rs79685996	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73093618	GATTTCTTTTTTTTT[G/T]GAGACCGAGTTTCGC	9873
rs79690010	snp	C/T	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:72894305	ATCCCAGTGTTCTGG[C/T]AGGCCAAGGCAGAAA	9873
rs79725269	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72913821	AAAAAACCAAAAAAA[A/C]CCCAAAAAAAAAACA	9873
rs79727431	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72965711	CTCTTTCCCATTCTA[C/T]GTACACCCCTCACCC	9873
rs79745265	snp	G/T	0.0517044	0.152246	intron-variant	FCHSD2	GRCh38.p7	11:72918809	GAAGGCATTTCCTTA[G/T]GGAGACAAAAAGCAA	9873
rs79746021	snp	C/T	0.143959	0.226396	intron-variant	FCHSD2	GRCh38.p7	11:73070790	ATGGTGACCTTAGAG[C/T]GTCACCATTCACTTA	9873
rs79813422	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72893750	GAGACTCTGTCTCCA[A/C]AAAAAAAAAAAACTC	9873
rs79836775	snp	A/G	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73080467	TATGTATTTAACAAA[A/G]AAAAGACCAAGTTTA	9873
rs79856396	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72886825	TCTCCCTATCTAGAG[C/T]AGGGAGTATTAGCCT	9873
rs79892128	snp	C/T	0.039522	0.134904	intron-variant	FCHSD2	GRCh38.p7	11:72888769	GGGAAGATAGGTGTG[C/T]GCCCCCATGCCCGAC	9873
rs79906268	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73122302	CAAGTACAAAAACTT[C/G]CCCGTATTAGAGACT	9873
rs79929666	snp	C/T	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:72885385	AGACTTAAATACTTG[C/T]ATTAGAAGAGGTGAG	9873
rs79947899	snp	A/G	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73094743	ATTATCAGCAAATTG[A/G]TAATTGTTTAATAAA	9873
rs79959847	snp	C/G/T	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:73106714	GCTGTGTTTTTTCTA[C/G/T]GTTCAGAATCACAAA	9873
rs79982450	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73006495	TGCTAGACTTAAAAA[A/T]TACCATGGAATTTAA	9873
rs79999406	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72861932	GCGAAACGCCGTCTC[A/C]AAAAAAAAAAAAAAA	9873
rs80012052	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72858031	TAGCATAAAGATTAA[A/C]TGAAGTAAAATATTT	9873
rs80012643	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72882370	CTCAAAAAAAAAAAA[G/T]TACAGAGTAGAATGA	9873
rs80015550	snp	C/G	0.0240643	0.107019	intron-variant	FCHSD2	GRCh38.p7	11:73088548	TTCCTTTACTTTCTT[C/G]TTTTGCTTTCCATAA	9873
rs80033263	snp	A/T	0.0715223	0.175059	intron-variant	FCHSD2	GRCh38.p7	11:72938944	AAAAATATAGTAAGG[A/T]TAGGGTCACAGAAGT	9873
rs80057058	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72866271	TTTTTGTTTTGTTTT[G/T]TTTTTTTTGTTTTTT	9873
rs80096155	snp	C/T	0.0383715	0.133092	intron-variant	FCHSD2	GRCh38.p7	11:72986625	GTGTTTGGGGATATT[C/T]CCAGTTCTCCTTTTT	9873
rs80113739	snp	A/G	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73051750	CAACAAAAAAAATTT[A/G]AAATAAATAGTAGTG	9873
rs80114378	snp	C/T	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:73040800	ACTAATCCGACTGTG[C/T]TATAAAATACTAAAA	9873
rs80115797	snp	A/G	0.0189856	0.0955633	intron-variant	FCHSD2	GRCh38.p7	11:73003276	AGAAATAACAAAAAT[A/G]CCTGCACCACTTACC	9873
rs80119927	snp	A/G	0.144969	0.226867	intron-variant	FCHSD2	GRCh38.p7	11:73047759	TCAAAATGCTATAAA[A/G]TGTATTGACTTTTTT	9873
rs80126159	snp	A/C	0.0279526	0.114869	intron-variant	FCHSD2	GRCh38.p7	11:73125862	CTATTATATAAAACA[A/C]TTCTTTTAGTAAAAC	9873
rs80146192	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73106407	TGAGACTCTGTCTCC[A/C]AAAAAAAAAAAAAAA	9873
rs80174420	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72959974	AAGCACAGATATATA[A/G]GAAGAAACCTACACA	9873
rs80194265	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73065133	GGCAAACCAAATCTA[C/G]CAGCACACCAAAAAG	9873
rs80196167	snp	A/G	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:72880445	CATCCCAGAAATAAT[A/G]TACTTATAGCCAACC	9873
rs80212858	snp	G/T	0.0168055	0.0901129	intron-variant	FCHSD2	GRCh38.p7	11:72880611	AAAATGATTAAAGAC[G/T]TTAAAAATAAACCCA	9873
rs80213802	snp	C/T	0.0260105	0.111035	intron-variant	FCHSD2	GRCh38.p7	11:72918184	ATTATTTTCTTAACC[C/T]TCTTTTTGGATCATT	9873
rs80262507	snp	A/G	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73134775	CTGATCGACAGCTCA[A/G]TGTATCAAAAAATAA	9873
rs80285823	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73006571	CTCACCTTATGCCTA[C/G]ATTACTGCAACAGTC	9873
rs80298780	snp	G/T	0.0298908	0.118541	intron-variant	FCHSD2	GRCh38.p7	11:72888682	GGAGTTCAGAGGCAT[G/T]ATCTTACCTCAATGT	9873
rs80316970	snp	C/T	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72981113	CTGTACTGCAGACTA[C/T]AGAATTAGCATGAGG	9873
rs80319951	snp	A/G	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73099808	GGCTAGAAAGAGTGC[A/G]AAGGGAAGCCAGGAG	9873
rs80333510	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73065308	ACAAAATTAAACAGC[A/G]CTTCATGCTAAAAAC	9873
rs80333555	snp	G/T	0.0267878	0.112589	intron-variant	FCHSD2	GRCh38.p7	11:73014607	AAGAAATCATCTGAT[G/T]TCAATCATCACTGAC	9873
rs80354696	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73128867	GTCAGGCTATAATTT[A/C]TTTTTATTTTTATTT	9873
rs80356403	in-del	-/A	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73003032	AATGTATTAACTATG[-/A]AGACTGTACAATAAA	9873
rs111265747	snp	G/T	0.0298908	0.118541	intron-variant	FCHSD2	GRCh38.p7	11:73111054	GCTATTATTTCAGGG[G/T]TTTTTTTTAATGTTT	9873
rs111271662	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72901988	CAAGTGATTCTCCTG[C/T]TTTAGCCTCCTGAGT	9873
rs111288078	snp	C/T	0.5	0	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72989004	GTACTGCATGAGCCA[C/T]CTGTTCAGTCTCAAA	9873
rs111307075	snp	A/C	0.0425829	0.139564	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141695	CGGAAAGGCAACTCA[A/C]ACGCGCGCCCCCCAC	9873
rs111320541	snp	C/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73084521	TCAGCCTCCTAAGTA[C/G]CTGGGACTACAGGTG	9873
rs111327773	snp	A/G	0.0456336	0.143994	intron-variant	FCHSD2	GRCh38.p7	11:73104600	TTGAGACAGACTCTC[A/G]CTCTGTCACCCAGGC	9873
rs111335495	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73022368	ATGTAAGAAACCCTG[A/C]AGAATCTACCAAAAA	9873
rs111344181	snp	C/T	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:73013904	AGGCATGAGCCACCA[C/T]GCCCAGCCTAACTAT	9873
rs111374724	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73064166	TACATGGAAATTGAA[C/T]AACCTGTTCCTAAAT	9873
rs111376558	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72928848	TTTAGCATTAGGTAT[A/T]TCTCCTAATGCTATC	9873
rs111377330	snp	C/T	0.0287284	0.116357	intron-variant	FCHSD2	GRCh38.p7	11:72956533	AATCAACAGCATTAA[C/T]TTCTCTTACTTCTGG	9873
rs111386020	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72925217	GAAAAGAAAATCAAA[A/G]TTCTGCTGGTACTTC	9873
rs111390711	in-del	-/A	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73068505	TATACTCCTGAAGTT[-/A]AAAAAAAAGTTGAGA	9873
rs111394825	snp	A/G	0.5	0	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72887551	TGATACAGCAGCTCC[A/G]TGACACTCCAGATCA	9873
rs111425392	in-del	-/A	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73032585	TTACCTTCCTAACTG[-/A]AAAAAAAAAAAGCAC	9873
rs111426684	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72909964	GCCCAGCTGCCCATT[A/G]TCTGGGAGGTGAGGA	9873
rs111427631	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72890138	CATAAAACCATTAAA[A/G]ACCATAAGCTTTTTG	9873
rs111437116	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72948074	GTGCAGTGGTGCGAT[C/T]TCGGCTCACTGCAAC	9873
rs111482231	in-del	-/AAAA	0.0275645	0.114116	intron-variant	FCHSD2	GRCh38.p7	11:73054223	TCTGGTCCTTTGCAG[-/AAAA]AAAAAAAAAAGTTTG	9873
rs111484239	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72958584	ATGTAAACACCACGG[A/G]ACAAAATCTAATAAG	9873
rs111490917	snp	C/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73134347	TGGTGGTGCATGCCT[C/G]TGGTCCCAGCTACTC	9873
rs111536891	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73128903	TTGAGACAGAGTCTC[A/G]CTCTGTTGCCCAGGC	9873
rs111553274	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72954764	GAAAGCCAGATTTAT[A/C]AATGGTAAGGAAGAT	9873
rs111573314	snp	C/T	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:72928145	GCTGGATAATGAGTA[C/T]GTGGGGGTCATTATA	9873
rs111577880	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969552	CACAAAGTGGAACTT[C/T]AGGCAAAATTATCCT	9873
rs111599136	snp	G/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72885472	TCTAGTTTGGCATAC[G/T]ATGGAAATAATAGGT	9873
rs111602928	in-del	-/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73087720	AAAAAAAAAAAAAAA[-/T]TTTTTAAAATAAATT	9873
rs111611038	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73030944	AATTTCTGCTATTTT[G/T]TATCCTTTGACCTAA	9873
rs111615035	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72987142	TCTTCCTTCTATGGT[C/G]TCTCCTAATGTGTGC	9873
rs111616537	snp	A/C/T	0.0291435	0.117316	intron-variant	FCHSD2	GRCh38.p7	11:73065888	AATATTCCATGCTTA[A/C/T]GGCTAGGAAGAATCA	9873
rs111676821	snp	C/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73039386	AGCTGGGCATGGTGG[C/G]GCGTGCCTGTAGTCC	9873
rs111678355	in-del	-/A	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72961177	AGCTGCTCTACAAGT[-/A]TATCAAATCCAGGTG	9873
rs111686502	in-del	-/G	0.342134	0.232404	intron-variant	FCHSD2	GRCh38.p7	11:73039249	TCTGCAGGGTGCAGT[-/G]GCTCACACCTGTAAG	9873
rs111710083	snp	C/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73119648	GAGATGGGATTTCAC[C/T]GTGTTGCCCAGGTTG	9873
rs111749204	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73119541	ACAATTATAGCTCAC[C/T]ATAACCTCAACCTCC	9873
rs111762225	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73096370	ACATGTTGAAACCCT[A/G]CCTCTACAAAAAAAA	9873
rs111777107	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73056837	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG	9873
rs111785565	snp	C/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72887938	AACATTACATAAGTG[C/G]AACACTGAATTTGAG	9873
rs111796479	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73104586	TTACTTATTTATTTT[C/T]GAGACAGACTCTCGC	9873
rs111804015	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73134102	ATAAATAAAGCCTTA[A/T]AAAAAAAAACTCTAG	9873
rs111857648	snp	C/T	0.0275645	0.114116	intron-variant	FCHSD2	GRCh38.p7	11:72999076	ACCATCATTTGAACC[C/T]CTAGATCCACCCATG	9873
rs111873122	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72946703	ACAGAGTAATAGCTA[A/C]CATTTACAGAATATC	9873
rs111883118	snp	A/T	0.0126979	0.078662	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841011	GTTGTTGAGCAATAA[A/T]GCTGATGCAAGGCTG	9873
rs111890322	snp	C/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73098697	CTTCAACAAATGGTG[C/G]CAAGACAAGATTTCT	9873
rs111918239	snp	A/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73043113	GAGTGGTGAAAGTGG[A/G]CATCCTTGTCTTACT	9873
rs111941738	snp	A/G	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73113494	CCACCTCAGCCTCCT[A/G]AGTAGCTGGGACTAC	9873
rs111948912	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836971	CTTCCAAAAAATATT[C/T]TAAAATACAACAAAA	9873
rs111960308	snp	A/C	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73129726	TCATCCCAAAACCAT[A/C]CCCCTGACCCCACCC	9873
rs111962346	snp	A/C	0.0437281	0.141251	intron-variant	FCHSD2	GRCh38.p7	11:73125346	AATAACTGTAATTAG[A/C]CCATTGTAAGGTCGT	9873
rs111970625	in-del	-/A	0.0287454	0.116389	intron-variant	FCHSD2	GRCh38.p7	11:73002598	ACATTTTAAAATAAT[-/A]AAAAAAATGAAAAAG	9873
rs111971075	snp	C/T	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:73003784	AAAATTTTATTTCAC[C/T]AGGTTTCATATGAAG	9873
rs111981480	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72983714	ATTCTGCCTAGCTTC[A/T]ATAATTTATTGAAAC	9873
rs111992518	snp	A/G	0.0130921	0.0798413	intron-variant	FCHSD2	GRCh38.p7	11:73081941	GGCGCGGTGACTCAC[A/G]CCTGTAATCCCAGCA	9873
rs112011198	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72965078	ACAGGCATGAGCCAC[C/T]GCGCCTGGCCAATCA	9873
rs112027563	snp	C/T	0.0441095	0.141807	intron-variant	FCHSD2	GRCh38.p7	11:72917953	AAGGCCATTGGAATT[C/T]TGATAGGGACTACAT	9873
rs112033048	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72897910	TTTACTTTTTCTAGA[A/G]AGAGCTCTGGCTTTC	9873
rs112040956	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72865008	TAGCATGATACAGAA[A/G]GCAGAGTTAATACCC	9873
rs112074658	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72854463	TAGAGACAGGGTCTC[A/G]CTCTGCTGCCCAAGC	9873
rs112110292	in-del	-/T	0.365646	0.221644	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143596	CCATGCCCAGGGAGG[-/T]TTTTTTTTTTTTTTT	9873
rs112118937	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72845458	AAAAAAAAAAAAAAA[A/C]AAACAACAACAAACA	9873
rs112120710	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73051238	GAAAATCAGTTGAAC[C/T]CAGGGGATTGAGGCT	9873
rs112137719	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72936108	ATCACTCTGGGAAGA[C/T]ACTGACCGTTCTTGA	9873
rs112187663	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72853054	TACTAGGCTTAGTAC[A/C]TGGGTAGTGAAACAA	9873
rs112195448	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72905804	TAGTATTCCATGGTG[C/T]ATATGTGCTATATTT	9873
rs112202410	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72883935	AGACCGTGTCTCAAA[A/G]AAAAAAAAAAAAAAT	9873
rs112204807	in-del	-/T	0.0279526	0.114869	intron-variant	FCHSD2	GRCh38.p7	11:73057328	AAGCAAAACAGAAGC[-/T]AAAGAATCACAAGGA	9873
rs112218116	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72992696	GTGCTGGGAATACTG[C/G]CTAGCCATATGTAGA	9873
rs112222854	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72924239	CACCACTGCATCTGG[C/T]TTACAAGTTTTAAAT	9873
rs112237652	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73077109	TCTCAAAAAAAAAAA[A/T]AAAAGAAAAAGAAAA	9873
rs112268354	in-del	-/A	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73038348	CCCTGTCTCTTTAAG[-/A]AAAAAAAAAAAAAAG	9873
rs112278425	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72872156	ATTTTTGGCTTAGAG[A/G]CACTCCAATTGGTAA	9873
rs112283538	snp	A/G	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73079351	ACAGGTACCCGCCAC[A/G]ACGCCTGGCTAATTT	9873
rs112314567	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72926491	GCAGAGACAACTTGC[C/T]AGCAGAGAGGGGAGC	9873
rs112325687	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72890293	CATGCCAACCTACTA[C/T]GGTGATAAAATCATT	9873
rs112402361	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73100930	CTTCTGTCTGACAAC[A/C]CTTTTCTCAGAGCTC	9873
rs112406958	snp	A/G	0.281313	0.248031	intron-variant	FCHSD2	GRCh38.p7	11:73093665	GGAGTGCAATGACGC[A/G]GTCTTGGCTCACCAC	9873
rs112420782	snp	C/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72998963	TTAAGATTTATAAAT[C/G]TGGCACATTGGGGGT	9873
rs112443096	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72914099	AGCTCGCTGCAAACT[A/G]CGCTTCCTGGGTTCA	9873
rs112475514	snp	C/T	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73093772	ATGCCGAGCTAATTT[C/T]TTTTGTATTTTTAGT	9873
rs112512641	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958128	CACATGAAAACCTCA[A/G]CAATAAGTGTTCCCA	9873
rs112513234	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044554	TGCACTCCAGCCTGG[A/G]TGACAGAGTGAGACC	9873
rs112539842	in-del	-/A	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73134100	TATAAATAAAGCCTT[-/A]AAAAAAAAAAACTCT	9873
rs112576724	in-del	-/T	0.0509478	0.151255	intron-variant	FCHSD2	GRCh38.p7	11:73054682	CTTTTCCTGTTATAA[-/T]TTTTTTTTTTCAGAC	9873
rs112582480	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72940700	GGATTCATGTTCACC[A/G]TGGTGGCAGAAAACG	9873
rs112603695	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72931545	GCCAAGGCAGGTGGA[G/T]CACAAGGTCAGGAGT	9873
rs112614182	snp	C/G	0.097727	0.198275	intron-variant	FCHSD2	GRCh38.p7	11:73120153	ATTATCTCCCACCAG[C/G]TCCCTCCCACAACAC	9873
rs112614512	snp	A/G	0.0799831	0.183287	intron-variant	FCHSD2	GRCh38.p7	11:73082206	GCTGGGCGTGATGGC[A/G]TGTGCCTGTCATCCC	9873
rs112633302	snp	C/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72905600	CCTAGCCCCCCACCC[C/G]CCGACAGGTCCCAGT	9873
rs112656518	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73098538	ATTGGGTGGAGTGTT[A/C]TATATACACCTGTTG	9873
rs112657585	snp	C/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72909566	CTAGACGGGGTGGCA[C/G]CTGGGCAGAGGCGCT	9873
rs112680047	snp	A/G	0.0372196	0.131242	intron-variant	FCHSD2	GRCh38.p7	11:72978920	GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC	9873
rs112681233	snp	C/T	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:73021513	GCTAAATGATGAGAA[C/T]ACATGAACACATAGA	9873
rs112706814	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141494	CTAAACAATCACACA[C/T]GCACAAGGCTCTGCA	9873
rs112721728	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72947871	CAAATTCAAGACTAT[A/G]TTTTACATATTATTT	9873
rs112722227	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72934981	TCCAGGTAGCTATTA[A/G]GCCACACACTCCCTT	9873
rs112731104	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72882691	AATAAAAAATTAAGA[A/G]GCCAAAAAAGGAAAC	9873
rs112742843	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73028399	GGGCCTGTAGCCCCA[C/T]TGTTTTGGCCAATTT	9873
rs112744819	snp	A/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72847955	CCTCATTTTCCCAAA[A/G]TGTTGGGATTACAGG	9873
rs112748940	snp	A/G	0.0111196	0.0737302	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142160	CGGAGACGGCGAGGG[A/G]GCGGGGGCCCCAGGA	9873
rs112752699	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72977304	GTAATACCCTGTAAG[A/C]ACAGGCAATCAAAGC	9873
rs112759795	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72907033	TGGCCATTTGTTTGC[A/G]TCCTCTTTTATTTCG	9873
rs112763936	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72865590	TCCCTTCCTTCACAA[C/T]GAGAACAGCCCTTCT	9873
rs112778193	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952578	GATCTACCGGCCTCG[A/G]CCTCTCAAAGTGCTG	9873
rs112803780	in-del	-/CA	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73082316	CACTCTAGCCTGGAT[-/CA]CAGAGTGAGACTTGT	9873
rs112806939	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73086269	CAAAAATTAGCTGGG[C/T]GTGGTGGTGCGTGCC	9873
rs112820916	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73132718	AGTCCTAGCTACTCC[A/G]GAGGCTGGGGTGAGA	9873
rs112825943	in-del	-/TTAA	0.097727	0.198275	intron-variant	FCHSD2	GRCh38.p7	11:73033938	AAACATTCAATAATG[-/TTAA]TTGTTTTAAAGAAAT	9873
rs112858988	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72921267	TTTAATCTATCAAAT[C/T]TTGAAGAAAAGTCAT	9873
rs112897475	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73114839	TCTCCTCTTCTCAAG[C/T]GGAAGGAGGGGGTCT	9873
rs112943178	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73088776	AAAATGAACTAGTTC[A/C]CACTTTCACCATTTA	9873
rs112953894	snp	C/G/T	0.0283406	0.115616	intron-variant	FCHSD2	GRCh38.p7	11:72985179	TCACAATAAAATTAC[C/G/T]AAATATATTATTAAA	9873
rs112954419	snp	A/G	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:72908845	TTTTTGTAGAGATGG[A/G]GTTTCACCATGTTGC	9873
rs112962977	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73014154	TTTTTTTTTGGGAGA[C/G]AGAGTCTCACTCTGT	9873
rs112980303	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73004128	AAAAAAAAAAAAAAA[A/T]AAAAAAAAGGATATC	9873
rs113065770	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73138880	GCCAAAGTGCTGGGA[C/T]TACAGGTGTCAGTGA	9873
rs113101952	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73077104	CTCTGTCTCAAAAAA[A/T]AAAAAAAAAGAAAAA	9873
rs113102552	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73133972	ACATTTTAAATTGGC[A/G]TGACGATTGTACAAT	9873
rs113107956	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72870856	AGTGAGCCGAGATTG[C/T]GCCACTGCACTACAG	9873
rs113155918	snp	C/T	0.0130921	0.0798413	intron-variant	FCHSD2	GRCh38.p7	11:72886546	GGCATTCTTTATGCC[C/T]TTCTAACAAGAACCT	9873
rs113159872	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73058797	GGTCTTGAACTTCTG[A/G]CCTCAGGTGATCCGC	9873
rs113160782	in-del	-/AC	0.0640965	0.167152	intron-variant	FCHSD2	GRCh38.p7	11:73121174	TATACACATACACAT[-/AC]ACACACACACACACA	9873
rs113169066	snp	C/T	0.0433465	0.140692	intron-variant	FCHSD2	GRCh38.p7	11:72966929	AGTGGCCGGGCGCGG[C/T]GGCTCACGCCTGTAA	9873
rs113180330	snp	C/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72859824	AACTCACACAGGTCT[C/G]AGAATAACTCCTGCT	9873
rs113188552	snp	C/G	0.00755907	0.0610114	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843738	ACCATAACAAAAACT[C/G]AAGAAACTGAATCCT	9873
rs113189295	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73071269	CGTGCATACACATGA[A/T]ATCTATAATGGAGGC	9873
rs113195592	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73118054	AGGCCCAGTGGCTCA[A/C]ACCTGTAATCCCAGC	9873
rs113196005	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73056822	GCGCGGTGGCTCACG[C/T]CTGTAATCCCAGCAC	9873
rs113199051	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72995764	TGAGTATGACAGAGA[C/T]ACAATAATAAACTTG	9873
rs113207050	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72907599	GAGATAATCACGTGG[G/T]TTTTTTTTTTTTTTT	9873
rs113219882	snp	C/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72887906	TATGGCATTAAGTTT[C/G]AGGTGGTTTGTTAAG	9873
rs113229757	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72853234	AGGATGCCAAGACCA[C/T]TCAGTGGAGGAAAGG	9873
rs113245631	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73074319	ATATCATAGAATAAA[A/G]CTCTGTATGTGCAAG	9873
rs113246963	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73133736	AGGCGGAGGTTACAA[C/T]GAGCCGGCATCGCGC	9873
rs113249286	in-del	-/A	0.0456336	0.143994	intron-variant	FCHSD2	GRCh38.p7	11:72878952	CTCTACTAAAAATAC[-/A]AAAAAAAATTAGCTG	9873
rs113274192	snp	A/G	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72896291	GTGTATTCTCATTCC[A/G]ACTGGGAAACCTGAG	9873
rs113275345	snp	C/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72971596	GAGCACCTCTAGGAG[C/G]TGAGAATGACCCCAG	9873
rs113285427	snp	A/C	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:72883772	CCCATCTCTACAAAA[A/C]AATAGAAAAATTAGC	9873
rs113290402	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72878570	ACTAGGAAGAAAGTA[C/T]TCAAGGACTAACGGG	9873
rs113292837	snp	G/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72940503	GTAAGCCAAGATGGG[G/T]GCATACCCGCACATC	9873
rs113309736	in-del	-/A	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73016303	GTGAGGCTCTGTCTC[-/A]AAAAAAAAAAAAAAC	9873
rs113313804	snp	A/G	0.0185938	0.0946107	intron-variant	FCHSD2	GRCh38.p7	11:73105023	ATAATCCCTGCTAGT[A/G]AAGTACTTCAAGTTT	9873
rs113326682	snp	A/G	0.279991	0.248195	intron-variant	FCHSD2	GRCh38.p7	11:72986271	TCGGAGTGCAGTGGC[A/G]TGATCTCTGCTCACT	9873
rs113340414	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72958292	GAAGGCTGAGGCAGG[C/T]GGATCACTTGAGGTC	9873
rs113340921	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890114	AAGTTACCAGAAGAG[A/T]AAGATCAGCATAAAA	9873
rs113346682	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73099307	AGAAAATAATAAGCA[C/T]TGGCCAGGATGTGAA	9873
rs113355644	snp	A/G	0.225005	0.248747	intron-variant	FCHSD2	GRCh38.p7	11:72874348	CATGCCACCATGCCT[A/G]GCTAATTTTTTAAAA	9873
rs113357204	snp	A/C	0.0260105	0.111035	intron-variant	FCHSD2	GRCh38.p7	11:72905093	TGTCCTAATTCCCAA[A/C]ACCTGTGAATGTTAC	9873
rs113361290	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73044898	ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA	9873
rs113414727	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72992594	AACAGAGCCCTCAGA[A/G]ATAATGCCACATATC	9873
rs113420418	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73012079	ATACTTATGTTCATA[C/T]AGAACTTATTCACTG	9873
rs113422490	snp	A/G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72928992	GTTTTTTGTCCTTGC[A/G/T]ATAGTTTGCTGAGAA	9873
rs113426864	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72977186	CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT	9873
rs113432199	snp	A/G	0.0448719	0.142907	intron-variant	FCHSD2	GRCh38.p7	11:73058770	ATGGGGTTTTACCAT[A/G]TTGGCCAGGCTGGTC	9873
rs113436162	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72916037	CACATGGGAACAACG[C/T]ACACTAGGGCCTACC	9873
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	9873
rs113474461	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72953357	TTTCAAAAAATCTTT[A/C]ATCTCTAATTCTGCT	9873
rs113495402	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73081930	ATTCAAGATCGGGCG[C/T]GGTGACTCACGCCTG	9873
rs113501899	snp	G/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73076107	GCCTGGGCAACAGAG[G/T]GAGAACCCATCTCAA	9873
rs113511914	in-del	-/AGTT	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73050994	AAGCAATTTGACATC[-/AGTT]AGTTTGTTATCTATA	9873
rs113549727	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73080296	AGCAAGACCCTGTCT[C/T]AAAAAAAAAAAAAAA	9873
rs113560473	snp	C/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73063765	TATACATGCACCCAA[C/T]ACAGGAGCATCCAGA	9873
rs113561444	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999445	CTGTCTCAGCCTCCC[A/G]AGTAGCTGGAACTAC	9873
rs113569546	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72989566	TCTGAGTAGTCTGAC[C/T]TGGTAAGTCCAAGGT	9873
rs113583431	snp	C/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:72862919	CAAGAAACAGACCCA[C/T]ACATATATGATTAAT	9873
rs113593662	snp	A/G	0.0505692	0.150756	intron-variant	FCHSD2	GRCh38.p7	11:73003738	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	9873
rs113605367	in-del	-/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72916242	AAAAAGGTTTATCAA[-/T]TTTTGTTAATCTTTT	9873
rs113620730	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72950571	TTGTGCCAGTACAAT[C/T]TGTTGAAAGACTATT	9873
rs113631395	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73131009	ATACTAATTGAGAAG[C/T]AACTATGATTGTTGA	9873
rs113645062	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72957031	AGTCTTTTTTTTTTT[C/T]TCTTCTTTTTTTTTA	9873
rs113655714	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72986399	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	9873
rs113666130	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73118571	TTCACCCACATTGAT[A/G]TGTGTATCCATAATT	9873
rs113673316	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900655	AATGTGAATAAGTCA[C/T]TGGCAAAAGCTGATT	9873
rs113674515	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72867625	TGGTAGATAGGCATC[A/G]ATAACCCAAATAGTG	9873
rs113694306	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72917141	AGGCACCCACCACCA[C/T]GCCCAGCCAATTTTT	9873
rs113701028	in-del	-/AA	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73050845	TAAGAAAAATAATAT[-/AA]GACTCAGAACACCCC	9873
rs113704626	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73085835	GTTACCACATTATTA[C/T]ATTCAAATCTCCAGT	9873
rs113725147	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73000813	ACATTCATTTTTAGC[A/G]GTTAATAAAACATAG	9873
rs113725323	snp	C/T	0.0973687	0.197999	intron-variant	FCHSD2	GRCh38.p7	11:73070572	GGTATTACAGGCGCC[C/T]GCCACCATGTCTGGC	9873
rs113726693	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72954082	CTATTACGCAGAGAA[C/T]AGACATAAAGGTAGG	9873
rs113741656	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72912903	AACTACCTGAGACTG[A/G]GTAATTTATAAAGAA	9873
rs113745103	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72854398	AATGTGGTATACATA[C/T]ATACGATGGAATATT	9873
rs113786055	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73134138	ATTAGATTACCTCTA[A/G]GATCTCTTTCTAGAT	9873
rs113807150	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73073083	AGCATTCTGCCAAAG[A/C]CTACAGGAAGTACTT	9873
rs113807821	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73015523	ATTTGTGTTCCATTG[C/T]CACCTGCCTTCTTTA	9873
rs113811560	in-del	-/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73021385	TGCAGCCATAAAAAA[-/C]AATGAGATCATGTCC	9873
rs113813070	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72894650	GTAAAAAGCATCTGG[A/G]TCTCTGTATTCCAAC	9873
rs113820890	snp	A/G	0.0185938	0.0946107	intron-variant	FCHSD2	GRCh38.p7	11:73091912	TGGTAGCGTGCACCT[A/G]TAATCCCAGCTACTC	9873
rs113840704	in-del	-/A	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72852662	GAGCAAGATTGTCTT[-/A]AAAAAAAAAAAGACA	9873
rs113841029	snp	A/G	0.0185938	0.0946107	intron-variant	FCHSD2	GRCh38.p7	11:73098837	CAGGGGCAATTCTTC[A/G]TGACCTTGGATTTTG	9873
rs113852908	snp	A/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73044447	TAGATGGGCATGGTG[A/G]CACACACCTATAGTC	9873
rs113873443	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73095150	TCTTATTTCTTATTA[A/C]TTAGGTGACCTTGAG	9873
rs113876218	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73030575	CTCTTACCTGATGAC[A/C]TTAACTTTGTAAAGA	9873
rs113877361	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73087574	GCCAGGCATGGTGGC[A/G]TGTGCCTGTAGTCCC	9873
rs113958825	snp	A/C	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:72982286	AAGGAAAGAACTTGC[A/C]GTTTCTGGCCAGAGT	9873
rs113972769	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73026757	CCTGCTAGGAGGTGA[C/T]TGGATCACAGGGGCA	9873
rs113974510	snp	A/G	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73081583	CCAGGCTGGAGTCCA[A/G]TGGCACTATCTGAGC	9873
rs113990312	in-del	-/A	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73094877	AAATATTTTTTAACG[-/A]GGCAAGCGGAACGAA	9873
rs114000235	snp	C/T	0.0295035	0.117819	intron-variant	FCHSD2	GRCh38.p7	11:72854809	GGAGTTATTGCTTAA[C/T]GGCCAGAAAGTTTTA	9873
rs114002424	snp	A/G	0.0107246	0.0724382	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840592	TTTCACAATTAGCCC[A/G]CTTTAATGCTCATAA	9873
rs114008928	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73080993	AATAAAATAAAGAAA[C/T]AGAAATAATCACCAG	9873
rs114049775	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73050582	GAACCCAGGCCCCCA[C/T]AATGGTTTTTCAGTA	9873
rs114054917	snp	G/T	0.0232847	0.105357	intron-variant	FCHSD2	GRCh38.p7	11:72921309	TCTCTGCATACAATG[G/T]GACATGTCAGCAAAC	9873
rs114173737	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72964111	ATATAGTTAATATTA[C/T]GGATGACACAATCAG	9873
rs114176709	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857140	TCCCATGGAAGGCAG[A/T]AAGAAGGCTGCAGTG	9873
rs114215734	snp	G/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73132314	AATACCTACCATTCT[G/T]GGCATTTCACCTGTC	9873
rs114220643	snp	A/G	0.0185938	0.0946107	intron-variant	FCHSD2	GRCh38.p7	11:72995425	CCAAAAACTGGGCCA[A/G]GTGCGGTGGCTCACA	9873
rs114237301	snp	A/G	0.030665	0.119967	intron-variant	FCHSD2	GRCh38.p7	11:72890655	GTGCAAGGTACTATG[A/G]AAAGTGCTTCATATA	9873
rs114243110	snp	A/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72935879	CAATGCTGTTTTTCT[A/G]TAAAGCTTGTGTTAT	9873
rs114257207	snp	C/T	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:73023735	CTTCTGGCAGCTTTA[C/T]TGATAAACTTGGCAA	9873
rs114258122	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143250	GCCTTTCTAAAGGTT[A/G]CACAGCAGGACTAGA	9873
rs114259149	snp	A/T	0.0244538	0.107838	intron-variant	FCHSD2	GRCh38.p7	11:73074979	ATAAATCAATAAGAG[A/T]AAAGCCAACAAGAGA	9873
rs114266847	snp	G/T	0.030665	0.119967	intron-variant	FCHSD2	GRCh38.p7	11:72877055	CGGCTCAGTGCAGCC[G/T]CAACCTCCAGGCTGC	9873
rs114296380	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73133289	ATCCAAAAGAAAAAC[A/T]TATATCCATACAAAA	9873
rs114301773	snp	G/T	0.0471551	0.14613	intron-variant	FCHSD2	GRCh38.p7	11:72916072	GGTAGAGGGTGGAGG[G/T]TGGGAGGAGGGAGAG	9873
rs114327330	snp	A/G	0.021333	0.101051	intron-variant	FCHSD2	GRCh38.p7	11:73072066	AAACAACAAATGAGT[A/G]AAGACATACGCAGAC	9873
rs114328398	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73056416	ATACCCCCAAAATGT[A/T]ATCTTTTTAAAAATT	9873
rs114333094	snp	C/T	0.0221141	0.102801	intron-variant	FCHSD2	GRCh38.p7	11:73060987	AGAACTGTTGATAAA[C/T]AGAAGCAAAAGAAAA	9873
rs114340239	snp	C/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:72886160	CTTGTATTGGGTCCC[C/T]GAAAGATGCTTGCCC	9873
rs114409985	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73099603	ATATACATACAACCG[A/G]GTATTATCCAGTCAC	9873
rs114415082	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73109986	TGATACGATGTATCA[C/T]ACTGACTGATTTGCA	9873
rs114420234	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72918430	CAATGGTTAATAGCG[A/G]TGGTGAAAATGGGTA	9873
rs114435156	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73007856	TGTACTACAGTTATG[C/T]AAGATATTACCACTG	9873
rs114457721	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73042212	CTACAGGCATGCGCC[A/T]CTGCACCCGGCTGAG	9873
rs114465769	snp	A/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72942167	CACAGTAATGAGAGC[A/G]TTCTCACTCTATAAG	9873
rs114472634	snp	C/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73112263	TTTTCACCAGACATA[C/T]CACTCTAGGGTAAAA	9873
rs114495105	snp	G/T	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72941030	GGCTTGGAAAGGACC[G/T]TATGTTCCACCATGC	9873
rs114499039	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73017045	TGGAGTGCAGTGGCG[C/T]GATCATGGCTCAATG	9873
rs114500143	snp	C/T	0.0256215	0.110247	intron-variant	FCHSD2	GRCh38.p7	11:73058201	TATTCTTTAAAGGTA[C/T]TGGACCATTATTGTT	9873
rs114582333	snp	C/T	0.0232847	0.105357	intron-variant	FCHSD2	GRCh38.p7	11:72923887	GAGGTTGCAGTAAGC[C/T]GAGTTTGTGCTATTG	9873
rs114626975	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73041882	ATGTCAGTAGTTTTA[C/T]AGTTTTGGGTCCTAG	9873
rs114634336	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72951875	TTCAGTATAGCAGAG[A/G]AAGTCCTTACTCCCA	9873
rs114667785	snp	C/T	0.0448719	0.142907	intron-variant	FCHSD2	GRCh38.p7	11:72999615	GTGAGCCACCACACC[C/T]GGCCTTATCAAACAT	9873
rs114668595	snp	C/T	0.029116	0.117091	intron-variant	FCHSD2	GRCh38.p7	11:73092431	AGGCACAAGCCACCA[C/T]ACCTGGCCCGGCATC	9873
rs114673292	snp	A/G/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73055008	GGACTGTGGTTCCAC[A/G/T]TGGCTGGGGAGGCCT	9873
rs114675965	snp	C/T	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72995780	ACAATAATAAACTTG[C/T]TAATAACTTGAATAT	9873
rs114690823	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73051133	CTAGTCTGGGCTAAC[A/G]AAGTGAGACCCTGTC	9873
rs114705375	snp	A/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72994376	CCTTGAAACGACTCT[A/T]TGAAAAAGGTAGTAG	9873
rs114706437	snp	G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73110496	TGTTCATAGTACCCA[G/T]GAATAATCTTTTTAA	9873
rs114735374	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73024575	CATGGGGGTAAATTA[C/G]AGTCACAGACATCAA	9873
rs114739106	snp	A/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72926432	ATAGCTGGAGACGAT[A/G]GGATGGCCAGCTGCA	9873
rs114741122	snp	A/C	0.0337553	0.125452	intron-variant	FCHSD2	GRCh38.p7	11:72851045	TGGAGACTAAGTGAG[A/C]CAAGAAAGATTGCAC	9873
rs114764285	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73106377	CACCACTACACTCCA[C/T]CCTGGGTGACAGAAT	9873
rs114764446	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73093238	CTCTCTTAGACCCTG[C/T]CCTGTACACCTCTTC	9873
rs114766548	snp	C/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73138061	TAGGATACTAGTATA[C/T]TGCAAGCAAAATGTG	9873
rs114766719	snp	A/G	0.0551013	0.156571	intron-variant	FCHSD2	GRCh38.p7	11:73046035	TCATTTTGTCACCTA[A/G]GCTGAAGTGCAGTGG	9873
rs114769135	snp	C/T	0.0236746	0.106192	intron-variant	FCHSD2	GRCh38.p7	11:72873950	AAAAAAGGATACTAC[C/T]GTGCCACTTTAACCA	9873
rs114772218	snp	G/T	0.0158469	0.0875917	intron-variant	FCHSD2	GRCh38.p7	11:72937424	AAATATAAAGCCTTA[G/T]TGTTAATTCAGTAAA	9873
rs114773324	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:73101202	CATTTATTCATAAAA[A/G]GGCCACATAAAATAG	9873
rs114844612	snp	A/C	0.0162398	0.0886349	intron-variant	FCHSD2	GRCh38.p7	11:73078406	ACCTTTGTTTAGAAG[A/C]CCTAGTCAAAAGTCA	9873
rs114849157	snp	A/C	0.0185938	0.0946107	intron-variant	FCHSD2	GRCh38.p7	11:72867575	TCTATTACTTCCAGA[A/C]ACGAAGCATATTTAC	9873
rs114865273	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72931914	AATGCCATTGTTTCA[C/T]TGTTGTTGTTTTAAA	9873
rs114865497	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72995472	TTTGGGAGGCTGAGG[C/T]GGCCAGATATCTTGA	9873
rs114875020	snp	A/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72949117	CAAAGTTGTGCAACC[A/G]TCACCATTACCTAAT	9873
rs114876231	snp	A/G	0.0236746	0.106192	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839837	ATGGTTATCATAGCT[A/G]TGGAAGTAGATGAGG	9873
rs114895480	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72852741	GAAGACATGAAATCA[A/G]CCTAAATACTAATCA	9873
rs114905990	snp	A/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:73024043	AAGGGTGGTGAACTA[A/T]TATACATAGTATTGT	9873
rs114942058	snp	A/G	0.00426843	0.0459999	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841540	GGCTGGTCGTACAAC[A/G]GCAGTGGAGGCAGGG	9873
rs114983577	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72916714	GATATGTGATGTGCA[A/G]ATATTTTCTCTCATC	9873
rs115011804	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72987560	TGGCATTCCTTACTC[C/T]ATAGTTGAAAAGTTA	9873
rs115044150	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857094	CTAAACATTCCTTTT[C/T]TCCTCCTTTATTTGG	9873
rs115044314	snp	A/G	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72929494	TAGAGTTAATGCAGG[A/G]GATACAAAAATTAAG	9873
rs115089126	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73008454	TTGTTATTGGTAGTA[A/G]AAAGGGAGAATATCC	9873
rs115091392	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73049955	TTTGCTCAAGATAAA[C/T]AGAAACTAACTATAA	9873
rs115124293	snp	A/C	0.0228947	0.104514	intron-variant	FCHSD2	GRCh38.p7	11:72965520	TCTAATTACATTTGT[A/C]CATACTGCCATTATA	9873
rs115125910	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114919	AGTACTCCCTCGGAC[A/G]CCATGGCTGGTGTCT	9873
rs115153113	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73059079	TCAATTCAACAAACA[C/T]GGATATAAATGTAAA	9873
rs115160909	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72927813	TCCTGAATAGGGTCA[A/G]GAGCACCAATAGGTA	9873
rs115167696	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72919468	CTAAAGAGAATATAG[C/T]AGAAGATCATGGAAA	9873
rs115181409	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72987565	TTCCTTACTCTATAG[C/T]TGAAAAGTTAATATT	9873
rs115202509	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142640	GTGGCACGTTCCAGA[C/T]GCCTCCTGCCCTCCC	9873
rs115306402	snp	C/T	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:72923916	TGAAATACAGCTCTG[C/T]GTGACAGAGCAAGAC	9873
rs115313998	snp	C/T	0.0217236	0.101931	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836295	TCACACAATTCATTA[C/T]TCCTTAGGGTGGAGG	9873
rs115330229	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73095143	GAAGTGTTCTTATTT[C/T]TTATTAATTAGGTGA	9873
rs115373005	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73003127	GCAGGGAAACATATC[C/T]TGAACACTGATATAC	9873
rs115382841	snp	A/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:72916410	TTCCAATTCCTGGGC[A/T]CAAGTAATCCTCCCA	9873
rs115402459	snp	A/G	0.0189856	0.0955633	intron-variant	FCHSD2	GRCh38.p7	11:72867262	ATTTTTCTGGTACTT[A/G]GATCTCCAACATGAA	9873
rs115410165	snp	A/C	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72889727	TCAAATAAAACAAAA[A/C]AACACATATAGGATA	9873
rs115419800	snp	C/G/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72969837	TGGATGAAGTTTAAA[C/G/T]ACACACATTGGTTAT	9873
rs115426147	snp	A/G/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73017548	TCTCAAGTTCCTCCC[A/G/T]AACTTGGCAACAATT	9873
rs115430925	snp	G/T	0.0150695	0.0854849	intron-variant	FCHSD2	GRCh38.p7	11:72901872	CTATTCTGGTTTTTT[G/T]TTTGTTTGTTTGTTT	9873
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	9873
rs115470194	snp	C/T	0.0244538	0.107838	intron-variant	FCHSD2	GRCh38.p7	11:73098891	CAAAAGCACAAACAA[C/T]GAAGAAAAAACAGGT	9873
rs115480895	snp	C/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72848358	TCTATACCTGCTGTT[C/G]TCTTTGCTTAGAAGG	9873
rs115503432	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73090519	CGTGAGCCACCGCGC[A/G]CGGCCTACAATACTT	9873
rs115538474	snp	C/T	0.0275645	0.114116	intron-variant	FCHSD2	GRCh38.p7	11:72950457	TCAAAGAGTTTTATA[C/T]AGTTTTAGCTCTTAA	9873
rs115550866	snp	C/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72927420	GTCAGTGTAGGTTCA[C/T]CAATTGCAACAAATG	9873
rs115584766	snp	C/G	0.0248432	0.108648	intron-variant	FCHSD2	GRCh38.p7	11:72982504	GTTTTGGGAAAACAG[C/G]AAAGAATGACAGATA	9873
rs115665885	snp	C/G	0.0562307	0.157967	intron-variant	FCHSD2	GRCh38.p7	11:72929694	ATAAATATTTATATA[C/G]ACTTTGATTAAAAAG	9873
rs115666265	snp	A/C/G	0.00875309	0.0656392	intron-variant	FCHSD2	GRCh38.p7	11:73093054	AGGCTAAGGCCAGCC[A/C/G]CATGAGTAGTAATCA	9873
rs115677815	snp	A/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72997875	CTGGCTAATTTTTAC[A/G]TTTTTTGTAGAGACG	9873
rs115701249	snp	A/G	0.00494653	0.0494853	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840999	CATTTTACTTGAGTT[A/G]TTGAGCAATAATGCT	9873
rs115702074	snp	C/G	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:72928677	TTGAATCTTATTTAA[C/G]TAGGTGAGAGGAGGC	9873
rs115705219	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028719	TTGTAATCCCCATGT[A/G]TCAGGGGAAAAACCT	9873
rs115708254	snp	A/C	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73126738	ATACACAAAAAAGAA[A/C]ATACAATAAAAAGCT	9873
rs115718387	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73006551	CTACCCCGCTTTGAG[C/T]CACCCTCACCTTATG	9873
rs115721591	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73018771	CTGAGATTATGACCA[A/G]GTGGCTTTAATATAA	9873
rs115721767	snp	A/C	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73106210	CCAAGGAGTTCGAGA[A/C]CAGCCTGGGAACATA	9873
rs115726258	snp	C/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:72937653	TGGCCAAAATATTTT[C/T]TTAGAACCTACTCTG	9873
rs115736450	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72953669	TCTTAAATGTTATGG[A/C]AGGTTGTAATAAATA	9873
rs115780798	snp	C/T	0.0236746	0.106192	intron-variant	FCHSD2	GRCh38.p7	11:72965848	GCTCTACCTCATGAC[C/T]AGGATTAATCCATGC	9873
rs115888856	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72932509	TATTACACCTTCTCT[A/G]CAATGCAGTTTTTGG	9873
rs115894057	snp	A/G	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72878681	TTGATAATATACTAA[A/G]TAGATAAAAATCTAT	9873
rs115902490	snp	C/T	0.0279526	0.114869	intron-variant	FCHSD2	GRCh38.p7	11:73108268	TTAGATCTTTTCCTA[C/T]GAAGTTGTTTAAGCT	9873
rs115907550	snp	A/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72878525	TCTGGGCAGGAAAAA[A/T]ATAAGGTGAACACTG	9873
rs115930873	snp	G/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72980151	ATCGTCTCTGTAAAT[G/T]AGGAAGAAAACCCAC	9873
rs115933650	snp	A/C	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73132307	AATGCTAAATACCTA[A/C]CATTCTTGGCATTTC	9873
rs115942451	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73125173	AAATGATAACAGATG[A/G]AAACTCAAACCTGTA	9873
rs115967958	snp	C/T	0.000927558	0.0215155	intron-variant	FCHSD2	GRCh38.p7	11:72983792	AGTCATTATTTTATT[C/T]CTTACATCACTCTTG	9873
rs115976304	snp	A/G	0.0228947	0.104514	intron-variant	FCHSD2	GRCh38.p7	11:73103088	AAAAGTAAATCAGCA[A/G]TTATTTGAGGCTGAA	9873
rs116002987	snp	A/G	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:73123792	TTTCTCTAGTTACAG[A/G]TGCTGGCCAACTGAC	9873
rs116062710	snp	C/G	0.0221141	0.102801	intron-variant	FCHSD2	GRCh38.p7	11:72949587	CTTTCTACATTTCTG[C/G]ATTTGCCTATTCTGG	9873
rs116084245	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960046	CTGCTGTAAAGGAAT[A/G]TGTAAGGCTGGGTAG	9873
rs116085316	snp	G/T	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72916606	AAGCGTGAGCCACTG[G/T]GCCCAGCCTCCTTTG	9873
rs116113806	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73135843	TGGTCTCCTCCCCTC[A/G]AAATTCCAAAAGATA	9873
rs116118214	snp	C/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72997462	CCACAATGTCCAATA[C/T]TGTGAGTCATAATCA	9873
rs116210010	snp	A/G	0.0232847	0.105357	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841288	ATGAGCCGTGATCAT[A/G]CCACTGAACTCCAGC	9873
rs116210869	snp	A/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72928679	GAATCTTATTTAAGT[A/G]GGTGAGAGGAGGCCC	9873
rs116215431	snp	C/T	0.0248432	0.108648	intron-variant	FCHSD2	GRCh38.p7	11:73115256	ACTCTCCCTCCCTGA[C/T]ATGCAGAATCTCCAC	9873
rs116229484	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73057754	AGTCCCTAACCCTTT[A/G]AATCAGAGCTTCCCA	9873
rs116233754	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73043512	ATACAACTTTTATTG[C/T]TGTCTTTAAAAACTG	9873
rs116240892	snp	A/G	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:73001634	ACATTGTCTTTCAAC[A/G]ACATCATTTTACTCT	9873
rs116241211	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72924713	AATACACAAATTCTG[A/T]CCCAAAAGCACTGAG	9873
rs116245253	snp	C/G/T	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:72914053	AAGGAGTCTCACTGT[C/G/T]GCCCAGGCTAGAGTG	9873
rs116295237	snp	C/T	0.0252325	0.109451	intron-variant	FCHSD2	GRCh38.p7	11:73020359	TTTCATCCCTCAGCA[C/T]ACAGAGAAACTAATA	9873
rs116322355	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73041907	TCCTAGGTTTAAGTC[C/T]AATCCACTTTGAGAT	9873
rs116323406	snp	C/T	0.0228947	0.104514	intron-variant	FCHSD2	GRCh38.p7	11:72969123	CAGACTCCAGATGTC[C/T]CCTCCTCATTGTCAG	9873
rs116351371	snp	A/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73111329	TTTACAACTGTTATA[A/T]CTTCTTGCTAAATTG	9873
rs116352467	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73124991	TCAGAAATAATGAAA[A/G]CCAGAAGACACTGGA	9873
rs116356495	snp	A/C	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73028117	CAGGGGCACTGCCTA[A/C]TGGAGGGGTGAGAAG	9873
rs116394852	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72872260	GGTGACAAAGACCTT[C/T]TGGCACACAACTTTT	9873
rs116412856	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73061378	ACAAACCTGGGTGGC[C/T]ATTTGGGCAAACACC	9873
rs116417616	snp	C/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72989601	AAGAGAAGCACGAAA[C/G]CTGGGTACCACATAA	9873
rs116437116	snp	C/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72894680	CTACACGTTTGTACA[C/G]GTTCACAATCCCACA	9873
rs116526311	snp	G/T	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:73015536	TGTCACCTGCCTTCT[G/T]TAAGTTTCAATTGGG	9873
rs116529002	snp	C/T	0.0236746	0.106192	intron-variant	FCHSD2	GRCh38.p7	11:72869533	AATACTTGCTTTTTT[C/T]TTTTTTTAATAAAAG	9873
rs116539912	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73042416	CATCCCATTGTTCTA[A/T]GTGTCTGTATTTATA	9873
rs116591754	snp	A/G	0.0236746	0.106192	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840521	TTATTTCATCTTGGT[A/G]TTCCTCAAAGAGGCA	9873
rs116597116	snp	C/T	0.0185938	0.0946107	intron-variant	FCHSD2	GRCh38.p7	11:73041624	TACTGAGTTGAGTTT[C/T]TTATATATTCTGGAT	9873
rs116615223	snp	C/G	0.0248432	0.108648	intron-variant	FCHSD2	GRCh38.p7	11:73019639	TTATTCAAGTTAGTT[C/G]ACAGAGGCAGGAATC	9873
rs116625556	snp	A/G	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:72896316	CCTGAGGAAGTTTCC[A/G]TGTTTTTCCTGCCTG	9873
rs116626069	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72885799	CTACTTGGCCAGCAC[C/T]CTAAGATAGTGGTTT	9873
rs116667893	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73130532	TGCCTTGGGCTGCAA[C/T]GGCTGTCCCATTCAG	9873
rs116726729	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73054831	ACAGACATGTGGGCC[C/T]GGTGGCATGTGCCTG	9873
rs116727324	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73073149	GAGTACTGCAAATGA[C/T]TTTACCAACACCTCA	9873
rs116749689	snp	A/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72903985	TGAATAAGACAAACA[A/G]ACAAGGTTAGTATCT	9873
rs116752266	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72950855	CTTCCTGGGCACATG[C/T]TGTGGGACTACACTT	9873
rs116818176	snp	A/T	0.0232847	0.105357	intron-variant	FCHSD2	GRCh38.p7	11:72894732	TGAAAAAGAATAAGT[A/T]TTTTTTGGTAAGTTT	9873
rs116831617	snp	C/T	0.0252325	0.109451	intron-variant	FCHSD2	GRCh38.p7	11:73106319	GCTAAGGCAGGAGGA[C/T]TGCTTGAGCCCATGA	9873
rs116842217	snp	A/G	0.030278	0.119257	intron-variant	FCHSD2	GRCh38.p7	11:73060710	AAAATGGGCATGAAA[A/G]TAAGATAACTATTTC	9873
rs116845993	snp	A/G	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72954970	GCTTTTTCTACCCTC[A/G]CTCACCACTCAACAC	9873
rs116878858	snp	C/T	0.0165278	0.0893908	intron-variant	FCHSD2	GRCh38.p7	11:73137148	AGGCAACTGAAGTTA[C/T]CATGAATACCAAGAG	9873
rs116884791	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839858	GTAGATGAGGTCATT[C/T]GGCAAGAGTGCGTTC	9873
rs116885891	snp	C/T	0.0471551	0.14613	intron-variant	FCHSD2	GRCh38.p7	11:72997159	TCCAGTAGAGAACTA[C/T]AGCCGAGAGGCCAAA	9873
rs116923077	snp	C/G	0.0577344	0.159793	intron-variant	FCHSD2	GRCh38.p7	11:72966459	ACCACCACACCCGGA[C/G]TAAACTGAGCATATT	9873
rs117002492	snp	A/G	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73097145	ATAGCTAGAACTACA[A/G]GTATGCACCACCAGG	9873
rs117005908	snp	A/G	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:73128128	AGGAGAATCCTAAGA[A/G]GCCAAAATACAAAAA	9873
rs117006866	snp	C/G	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73035336	GCACCACTACTCCTG[C/G]CTTGTATTTTTTGTA	9873
rs117008121	snp	A/G	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73093333	CAGTGAGCTCTGAGA[A/G]TCCTGGCAAATTATT	9873
rs117021568	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72848000	CCCGGCCAACTCTAA[C/T]CATTAAATATAGTTT	9873
rs117023160	snp	G/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73035148	GTTTTTAGTTTTTAT[G/T]TTTATGTATGTATGT	9873
rs117024108	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72895750	TAACTGTCAGTATTG[C/T]TAATTCTAAAACGCA	9873
rs117054606	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72979146	TATGGGTGTAAGTCA[C/G]CATGCCCGGCCACAG	9873
rs117085272	snp	G/T	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:72915956	CTATCCTTAGCAAAC[G/T]AATGTAGGAACAGAA	9873
rs117127779	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907143	CATTATTTGGCTCTC[C/T]ATTACTGCTGGAATG	9873
rs117167659	snp	C/T	0.0158469	0.0875917	intron-variant	FCHSD2	GRCh38.p7	11:73058223	ATTATTGTTTTATGT[C/T]ATAAAATCAGCCAGG	9873
rs117174420	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046793	TCACCATGTTGCCCA[A/G]GCTGGTCTTGAACTC	9873
rs117181194	snp	A/C	0.0399052	0.1355	intron-variant	FCHSD2	GRCh38.p7	11:73074494	AAATGTGAAATATTA[A/C]ACAATAAAAATTCCA	9873
rs117191547	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72888712	TAACCTCCACCTCCC[A/G]GGCTCAAGCAATTCT	9873
rs117218917	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73080397	TGTAATTCCACTGTA[C/T]CTGCATACATTCATA	9873
rs117276035	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72925661	ATAACTGACGCACGT[A/G]TCCCAGGGTCCACCA	9873
rs117279208	snp	A/G	0.0189856	0.0955633	intron-variant	FCHSD2	GRCh38.p7	11:72937466	ATGCTGGCCAATTTG[A/G]GTATTCCTTACATTG	9873
rs117280763	snp	C/G	0.0209421	0.100162	intron-variant	FCHSD2	GRCh38.p7	11:72883215	CACAAAGAAAAGCTT[C/G]AACTATAACACTTCT	9873
rs117288769	snp	C/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72926938	TGAAAAAAATGGCGA[C/T]TTGGTGCACTAGTAG	9873
rs117298868	snp	A/G	0.0165278	0.0893908	intron-variant	FCHSD2	GRCh38.p7	11:72930521	CTTTGGGATCAGGAG[A/G]ATCACCTGAGGACAA	9873
rs117308472	snp	A/G	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:73070199	GGAAAGCAATCTCCA[A/G]AACAATATCCCTATA	9873
rs117331368	snp	C/G	0.0376037	0.131863	intron-variant	FCHSD2	GRCh38.p7	11:72966857	TATAGTTTGAGGAAG[C/G]ATTCCCTAAAGAAGT	9873
rs117337119	snp	C/G	0.0418186	0.138422	intron-variant	FCHSD2	GRCh38.p7	11:72858947	AGGACAGTGATCCCT[C/G]GGGGATGGGAAACAA	9873
rs117374082	snp	C/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73089586	TATATTTATATAATG[C/G]AATGTTATTCAGCCA	9873
rs117377192	snp	C/T	0.0193772	0.0965046	intron-variant	FCHSD2	GRCh38.p7	11:73020902	TACATTGAGACAGGG[C/T]CTTGCTCTGTCACCC	9873
rs117386734	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73060908	CACTATAGTGAGATT[C/T]CCGTGTTCATGAAGG	9873
rs117395638	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72876305	GTCCAGCCTGCGAGA[C/T]AGAGTGAGATGGTCT	9873
rs117437316	snp	C/T	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:73094609	TGACCACTTCATTTT[C/T]GCTACGATACTTGAC	9873
rs117438589	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029616	TTGTGGAGGTGCAGA[A/C]ACAGAGGTAGGAAGT	9873
rs117442324	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72964300	ACATCGAATCATGTA[C/T]TATTGTCTTTGCACT	9873
rs117466269	snp	C/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72981945	ATGTTCAAGCCACTG[C/G]ACTCTAGCCTGTTAT	9873
rs117484624	snp	C/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72845224	CCAGCAGTTTGAGAC[C/T]GGCCTGGGCAACATG	9873
rs117495951	snp	A/T	0.0327778	0.123752	intron-variant	FCHSD2	GRCh38.p7	11:73110098	TTTGCTAGTATTTTG[A/T]GGAGGATTTTTGCAT	9873
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	9873
rs117527774	snp	A/G	0.0418186	0.138422	intron-variant	FCHSD2	GRCh38.p7	11:73102427	AGGACCCATACACAA[A/G]TGTGTACAAAATGTG	9873
rs117545018	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870054	TGTTCCTCTGATCCA[A/T]CATGTGCTTGCGTGC	9873
rs117559934	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72987071	CAGTGTTTCCCAGGC[C/T]CTTCAGAATAAACAT	9873
rs117590031	snp	A/G	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73058852	GGATTACACGTGTGA[A/G]CCATCCCACCTAGAC	9873
rs117591835	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73078832	CACGTGATTCTCCTG[C/T]TTCAGTCTCCAAGTA	9873
rs117594886	snp	A/G	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:72991561	GCTGGTTCAACATAC[A/G]CTGATCAAGTGGGCT	9873
rs117610694	snp	C/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73070209	CTCCAGAACAATATC[C/T]CTATAAGTGTAGTCT	9873
rs117617770	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72971878	TTGTTACATAGCAAC[A/G]GAAATCAAATATAAC	9873
rs117624063	snp	A/G	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:73051320	ACTCTAGCTCTAAAA[A/G]ATAAAAAAATAAAAA	9873
rs117631429	snp	A/T	0.0360663	0.129354	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72844141	GCCATTTTCTGGAGG[A/T]TGTGAGTCAATGTGG	9873
rs117645057	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72994230	GTACTCTGTCCTTCT[C/T]AGTAAACCTCTTGTC	9873
rs117651646	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72875562	TCAAACTCCTGGCCT[C/T]AAACGATCCTTCCGC	9873
rs117664896	snp	C/T	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:73062601	AGAACATAAATGACC[C/T]GATGGAGCTGAAATA	9873
rs117678186	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900480	AAAAGTGAGATGAGA[A/G]TCACTGTTATTCTGA	9873
rs117705747	snp	C/T	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:73042549	TATTGAGGTCTTCTG[C/T]GGTTCCATACAATTT	9873
rs117707243	snp	A/G	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:73031988	AATATCCACCAAGAG[A/G]AACTATTAACTAAAT	9873
rs117733068	snp	A/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72904704	TTCTTTTTTTTACAA[A/G]AAAGTTTTTCAAATC	9873
rs117794201	snp	A/C	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73071905	TGACACATGATCTTA[A/C]TATATGTTCTTTAAC	9873
rs117801487	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73036226	TTTTAAAGGAAGAAA[A/G]ATATACAATTAGAAA	9873
rs117824058	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130721	AGACCCTCTCAAACT[A/G]TATTTCCTTCTCTGC	9873
rs117893776	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032940	CAGTGCCATTATCAG[A/C]CTAAAATGTGATTTA	9873
rs117932352	snp	A/G	0.0700422	0.173537	intron-variant	FCHSD2	GRCh38.p7	11:72913951	AACAAATGAAAAAAC[A/G]TACTATGCTCATGGA	9873
rs117943137	snp	C/T	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72986995	CCTCAAAGCGAGATC[C/T]TGAGGCCCAAATTCT	9873
rs117946797	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73015267	GATATTAACTAGCCA[C/T]GTCTAAATCTTTTGT	9873
rs117962776	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72933582	ATAAATGATACCCAA[C/T]TTATATTAGCCATAT	9873
rs117969824	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73040251	CAACCCAGCTCTTTT[C/T]CCAGGAACAGGAGAA	9873
rs117972485	snp	A/C	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73130984	ACATTTTAAGTTCTA[A/C]TTTGAAAGAATACTA	9873
rs117980813	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72998206	AAGATTTTTATATTG[C/T]TCATGAGGTAGTAAA	9873
rs117984489	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73095646	GCTCCAAAACTCAAA[A/G]CGGGAGTACCTTTGT	9873
rs118010414	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040539	CATTCTGTTGGTGAT[A/G]CCTTCCCTTGTCAAT	9873
rs118051917	snp	C/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836265	ATCCACCCCTGGGAC[C/T]GAGAAAATCTCCTTT	9873
rs118071307	snp	C/T	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:72997345	CTAAAACCAGAGATC[C/T]TAACAGAATCAAGGT	9873
rs118077937	snp	C/T	0.143284	0.226079	intron-variant	FCHSD2	GRCh38.p7	11:72853121	TATAACAAACCTGCA[C/T]ATGTACTCTTGCACT	9873
rs118109338	snp	C/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73006287	TCCAACTTGGATATT[C/T]AGTAGGCACCTTTAC	9873
rs118125226	snp	C/T	0.0174175	0.0916809	intron-variant	FCHSD2	GRCh38.p7	11:73088641	ATTCATAAACATGTA[C/T]ACACACTTTTTTTAC	9873
rs118141553	snp	G/T	0.0368353	0.130617	intron-variant	FCHSD2	GRCh38.p7	11:72877870	AATTAGCTGGGTATG[G/T]TGGCACATGTCTGTA	9873
rs118152894	snp	C/G	0.0376037	0.131863	intron-variant	FCHSD2	GRCh38.p7	11:73017097	AAACAATCCTCCCAA[C/G]TCAGCCTCCCAAGTA	9873
rs118185214	snp	C/T	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:72898822	GCAACCTCCACCTCC[C/T]GGGCTCAAGTGATCC	9873
rs137862963	snp	C/T	0.0260105	0.111035	intron-variant	FCHSD2	GRCh38.p7	11:72907841	CTCGTCATCTGCCCA[C/T]CTTGGCCTCCCAAAG	9873
rs137935783	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73010262	TTGGTTCTTTTTTAT[A/C]TCTCTCTTTGGTAAA	9873
rs137950141	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102749	ATAATGCATCAAGAG[C/G]TTCCTCACCAGATGC	9873
rs137962254	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73089834	ATTTTTATTTAACTA[C/G]ATAAGCATTTTCATA	9873
rs137966433	snp	C/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73048465	ACAACTCAAAAAGTG[C/G]AAATGGATTAAAACA	9873
rs137971113	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853231	ACAAGGATGCCAAGA[A/C]CACTCAGTGGAGGAA	9873
rs137979422	snp	A/C	0.144969	0.226867	intron-variant	FCHSD2	GRCh38.p7	11:72991008	GAATCAAACAGACGC[A/C]ATAAAAAATGATAAA	9873
rs137998102	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73125484	CCAAAGAAGGGGGAC[A/T]GCTTGAGCTCCACAG	9873
rs138009125	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950249	AATATTAAATCCTTT[A/T]CAGATATGTAATTTG	9873
rs138010437	in-del	-/AT	0.040671	0.13668	intron-variant	FCHSD2	GRCh38.p7	11:72938670	GTCTGGAGAGGGTCA[-/AT]TTTCATCATTCTTTT	9873
rs138014563	in-del	-/AATATCTGTTA	0.0437281	0.141251	intron-variant	FCHSD2	GRCh38.p7	11:73126608	AATACGAACTTTTAT[-/AATATCTGTTA]AATATCTGTTATGCT	9873
rs138023210	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72895271	TATACCCATTAAGGC[C/T]GGGGTGAAGAAATGA	9873
rs138050533	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000689	CTAATACACATCAAA[C/T]TATACCGATATTGTG	9873
rs138085044	snp	A/G	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:72941848	GCTTCAAAAAAAGAT[A/G]TCTTAAGGAAGTTAT	9873
rs138085724	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73094793	TGGAATACAGTGGCT[-/G]GTTTGTAAAGGTATT	9873
rs138086578	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72902711	TTATAAAGTTTAAGA[C/T]TTATTCTGCTATTTT	9873
rs138088346	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72927423	AGTGTAGGTTCATCA[A/G]TTGCAACAAATGTGC	9873
rs138094995	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73029930	AAAACAAAAGAAAAA[C/G]AAAAACAAAAACAAA	9873
rs138123962	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883361	CCAATCTAGAAAATG[A/G]AAAGGTAAGCCAAAG	9873
rs138191331	snp	C/T	0.0205511	0.0992634	intron-variant	FCHSD2	GRCh38.p7	11:72882672	TGTACAATTATTTTG[C/T]ATCAATAAAAAATTA	9873
rs138193944	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846871	ATATTAGGACATAAG[C/G]GTTTCTTCTTATATA	9873
rs138227849	in-del	-/TG	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:72935887	TTTTTCTATAAAGCT[-/TG]TGTTATCCTCTTGCA	9873
rs138232413	snp	A/C	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73065689	AATCAATGTGCAAAA[A/C]TCATAAGCATTCCTA	9873
rs138243522	snp	G/T	0.0134861	0.0810011	intron-variant	FCHSD2	GRCh38.p7	11:73058588	GTTTTTTAGGTTTAT[G/T]TCATTTTCCTTTTTT	9873
rs138253386	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72913394	ACACCTCAGCCTCCC[A/G]AGCAGCTGGGATTTC	9873
rs138317587	snp	A/G	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:72857676	GCTGGTCTTGAACTC[A/G]TGACCTCAGATGATC	9873
rs138320954	snp	A/G	0.000153988	0.00877327	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867899	CTGGTCACTGCAGGA[A/G]GGCGGGCCCATCGCT	9873
rs138330211	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022397	AAACCTCATGGAACT[A/G]ATAACTGAGTTTAGC	9873
rs138356958	snp	A/C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73118260	GCAGGCAGAGACTGC[A/C/G]GTGAGCCGAGACTGT	9873
rs138364507	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72954879	ATATCTATACATATA[C/T]ACACACACACACAGA	9873
rs138389902	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73029345	CACTGCGGCAAGATC[A/G]GTTTGATGCAATTAT	9873
rs138400377	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73104442	GCCTGGCTAATTTTT[A/G]GATTTTCAGTAGAGA	9873
rs138400995	snp	A/C/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72868246	AGCAAACTAAGGCAG[A/C/G]AACAGAAAACCAAAC	9873
rs138416817	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039405	TGCCTGTAGTCCTAG[C/T]TACTCCAGAGGCAGA	9873
rs138425398	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131544	AAAAAAAATAAAAAT[A/T]ACTACAAAAATTATC	9873
rs138432563	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902921	GAAAGCAAGAAGATA[A/G]TTTTTACACAAAAAG	9873
rs138434576	in-del	-/AG			intron-variant	FCHSD2	GRCh38.p7	11:72869443	TGGGGGGAGGGAAGA[-/AG]AGAGAGAGAGAGACA	9873
rs138442949	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73016874	TATAACAGGTGTCAG[A/G]GAGAGGTACAGGGAT	9873
rs138446983	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73107911	CTGCAATCGACATGG[A/G]TATCTTTTGGATATA	9873
rs138451046	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976483	CAAAGTCTCACTATG[C/T]TGCCCAGGCTGGTCT	9873
rs138452684	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72873502	TATCAGATACATGAT[G/T]TGCAAATATTTTCCC	9873
rs138471526	snp	C/T	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72955018	ATGTGTGGGGACTTT[C/T]CCACATGCCAAGCAA	9873
rs138480712	snp	A/G	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72962173	TCTGAGACCCTTTTA[A/G]GGGACCTGTGGGGTC	9873
rs138484535	in-del	-/ACACACACAC			intron-variant	FCHSD2	GRCh38.p7	11:72999867	TTTCTGCACAATCAG[-/ACACACACAC]ACACACACACAAACA	9873
rs138487138	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73060072	GGTAGGATACACTGC[A/T]ATCAGAGATGACTAA	9873
rs138510554	in-del	-/A	0.385741	0.209939	intron-variant	FCHSD2	GRCh38.p7	11:73078649	ATAAAAAAAAAAAAA[-/A]GTACTGGTTGCCATT	9873
rs138526473	in-del	-/TTTG	0.109108	0.206518	intron-variant	FCHSD2	GRCh38.p7	11:72923157	TCAGTTGTACCACAT[-/TTTG]TTTATTAATCAGGTG	9873
rs138562468	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73098914	AAACAGGTAAAATGA[A/G]CTTCATCAAAATTTA	9873
rs138622197	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124819	AAAGCATCAACCATT[A/G]AATGATGAACCCCAA	9873
rs138634237	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141466	CGGCTGGAGGGCTCA[A/G]AGCTGGTGCAGACTA	9873
rs138638149	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995229	TTTATCTTGCAGAAC[A/G]AAAAGCTGTTTTCCC	9873
rs138653886	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083119	TAAAGAAGAATAAAT[A/C]AACAAACTTGTAAAA	9873
rs138656618	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72978435	AGGTGCTCAATATCA[C/T]TGACCATCAGAGAAA	9873
rs138657916	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73074890	GCACTCCAGCCTAGG[C/T]GACAGAGTGAGACCC	9873
rs138664316	in-del	-/TA/TATA	0.118021	0.215066	intron-variant	FCHSD2	GRCh38.p7	11:73107035	TTTTGTTAGAAAAGC[-/TA/TATA]TATATATATATATAT	9873
rs138669194	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839561	GCGAGCTCTCTGCAA[G/T]GTATACCTGGCAGGA	9873
rs138725034	snp	G/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72942535	ATGCCTAGGAAAGAT[G/T]AGAAGGATATGCCAA	9873
rs138728187	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73034727	ATTTGCACAAAATGA[C/T]CTGCAAATTTTAAAG	9873
rs138758312	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72932982	CAAGTTAAAGGAGTA[A/G]TTGATTTCATAAAAC	9873
rs138765855	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72876752	TTCTATCAATTACTG[A/G]AAGAGGGATCCTAAA	9873
rs138767346	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72848070	CTGGACTATAAGAAT[G/T]ATGATTAGGCTTAAA	9873
rs138791840	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72948231	CAGGCTGGTCTTGAA[C/T]TCCTGGACTCAAGCA	9873
rs138797316	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852793	ATGTGGTACATATAT[A/G]CCATGAAATACTAGG	9873
rs138821268	snp	A/C	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73021452	CTTAGCAAACTAATG[A/C]AAGAACAGAAAACTA	9873
rs138825787	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114285	AGTGCTCTTCAGTCA[C/T]CTTGTGGTGAATTCT	9873
rs138831216	snp	A/G	0.000164275	0.00906148	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867924	ATCGCTCATTTTCCA[A/G]TTCTTCCATTACTTG	9873
rs138847212	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72881870	GCTGGGGCCGGGTGC[A/G]GTGGCTCACGCCTGT	9873
rs138856854	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839004	AAATGTTGTGAGCAC[A/G]TGCTTTCAACCTAGT	9873
rs138878062	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72863317	AGGGACAAAGAACTC[G/T]GACTTATTCTGTTTA	9873
rs138884204	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73055452	AGAGCTCTTTATCAG[A/G]AGAAGTATACAATGA	9873
rs138909479	snp	G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72963559	AAAAAATGTGGATTG[G/T]ATCAGCAGCCCCCAA	9873
rs138979720	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73061124	ACCTGGTTCATCTCA[C/T]TGGGACTGGTTGGAC	9873
rs139013046	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73013127	GCAAACTCTATACTG[C/T]GATATGTAAAGTCCT	9873
rs139013123	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908660	GTACCTTTCCATATG[A/C]CTGTCTGCCACTTAT	9873
rs139019742	snp	A/C	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73016352	CAACCAACCAACCAA[A/C]CAAACAAAAAACAAT	9873
rs139021724	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72912795	TATTACAGCTTTGAT[C/G]TTGTTACTTGTTTTT	9873
rs139024112	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73078632	AAAATAACAACTATT[C/T]TGATAAAAAAAAAAA	9873
rs139052840	snp	C/G/T	0.000171153	0.00924944	synonymous-codon, missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902567	GTCACAAGGCTGGAA[C/G/T]TGGAAGGGCTGGGGT	9873
rs139075918	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72971093	GTATAGACTTGAAGG[C/T]AAACTAAATGCTGTT	9873
rs139077318	in-del	-/AT	0.153	0.230415	intron-variant	FCHSD2	GRCh38.p7	11:72887076	TATATATATATATAT[-/AT]GAATATATGTCTCCA	9873
rs139080054	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73066305	GCCATATGCAGAAAA[C/T]TGAAACCGGATCCCT	9873
rs139093689	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73073821	AATAATAAAAACTGT[A/G]CATGTGCAAGGATTT	9873
rs139096262	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72933149	AACTTGCAGGGTAGG[C/T]AGATATGCAAGACAG	9873
rs139096647	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73116642	AAATCCTGGGCACAA[C/G]CTCCCGCGTCAGCCT	9873
rs139135376	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73069934	ATATGTAAAAAAACA[A/G]AGTCACAGAAAATTA	9873
rs139154031	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72917610	CGAAGACTGGGCCGA[A/G]TGCAGTGGCTGACGC	9873
rs139157139	snp	A/G	0.0248432	0.108648	intron-variant	FCHSD2	GRCh38.p7	11:73031080	GTATGAATCTGGATG[A/G]GTTCATCCAGAATAT	9873
rs139159296	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73119952	ATTGGACTTACAGTT[A/C]CACATGGCTGGGGAA	9873
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	9873
rs139167869	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018139	CTCAAATTGTCACAT[C/G]TGTGGTCTGTCAGAG	9873
rs139214762	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72972351	AGACCTCTATAAGAA[A/G]TTTGGTAGTTGGAAA	9873
rs139241556	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73109438	TGCAGAGATCTTTCA[C/T]TTCATCAGTTAATTC	9873
rs139242866	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73082368	AAAAAAAAAAGAAAA[A/G]AAAAAGCATTCAACA	9873
rs139250745	in-del	-/AA			intron-variant	FCHSD2	GRCh38.p7	11:73133814	AAAAAAAAAAAAAAA[-/AA]GTAACCATTATGCCA	9873
rs139268471	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959311	CTCGGCTCACTGCAA[A/G]CTCCACCCCCCAGGT	9873
rs139271142	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72879148	ACAAAAAAAAAGATA[C/T]TACAACTCTATCCAG	9873
rs139273875	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056526	CTTTGCTAAAATGAA[C/G/T]CAATTTAATCTTTCA	9873
rs139282498	in-del	-/ATA	0.499	0.0223418	intron-variant	FCHSD2	GRCh38.p7	11:72890387	TAAGAACAAAACAAT[-/ATA]ATAACAGCAACACAA	9873
rs139290743	snp	A/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73133742	AGGTTACAACGAGCC[A/G]GCATCGCGCCACTGC	9873
rs139295729	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72872287	TTTTTTTTTCTTTTC[-/TT]TTTTTTTTTTTTTTT	9873
rs139333874	snp	A/G	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:72978960	CTCTCAGGTTCAAGC[A/G]ATTCTCGTGCCTCAG	9873
rs139386488	snp	G/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72997726	TTTGTTTTGAGAAAG[G/T]GTCTCCCTCTGTCAT	9873
rs139395844	snp	A/C	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:73127468	TGTGCCTAGATCCCT[A/C]ATTAGTTACTGAAAA	9873
rs139404812	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897504	GTTATATGCAAATAT[A/T]ACATCATTTTATATA	9873
rs139411354	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841073	TTTGGGATACTGAGG[C/T]GGGAGGATTACTTGA	9873
rs139419717	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980171	AGAAAACCCACTTGC[A/T]AAGCATAAAAGAGAA	9873
rs139451596	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73031418	GAGGTGGAGGCTGCA[C/T]TGAGTTGTGACTACT	9873
rs139490055	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72884957	AATAATGAGGACTCA[C/T]ATTTTATATAACCAG	9873
rs139492265	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73096870	TCCATTCCTAGTTTT[C/T]TGAGTCTTTTTATCA	9873
rs139508122	snp	A/G	0.0248432	0.108648	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144440	GAATAGCGTGAACCC[A/G]GGAGGTGGAGCTTGC	9873
rs139515863	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72884286	AAAGCCAGTATTGCA[A/G]AATATAATAGTTGAA	9873
rs139520391	snp	G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73096551	GCAAAGGAAAGGAAA[G/T]GAAAGGAAAGGACAG	9873
rs139525599	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025574	GTGATGCAATAATCT[G/T]TACCACAACCCCCGA	9873
rs139527982	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:72983973	TATATTCCAATGAGA[C/T]GCAACATAGCCTGGC	9873
rs139557221	snp	G/T	0.0130921	0.0798413	intron-variant	FCHSD2	GRCh38.p7	11:72889708	ACAGAGCAAGCCTCT[G/T]GTCTCAAATAAAACA	9873
rs139562774	snp	G/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73115978	ACATAAAAGTAACCA[G/T]CACAGGGGCACAACT	9873
rs139568627	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73005310	CAAATCAGACTTTAG[C/T]GTCTACCACTCTTCT	9873
rs139588609	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72865134	ATGTCTAACAGTAGT[A/G]TTAATCATGTTTTCC	9873
rs139588810	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73099735	TGGGGCTGTCAAGCC[A/G]GACCAAAAAGGCTGT	9873
rs139631736	snp	C/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73013773	TAGCCTAGGAGCATA[C/G]CTTTTTAATCCTTAT	9873
rs139638060	snp	G/T	0.0205511	0.0992634	intron-variant	FCHSD2	GRCh38.p7	11:72945452	ATAAAAACCCTAGAA[G/T]AAAAGCTAGGCAATA	9873
rs139647968	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72939639	TTTTTTTTTTTTTGA[A/G]ACAGTGTCTCGCCCT	9873
rs139661814	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72854462	TTAGAGACAGGGTCT[C/T]GCTCTGCTGCCCAAG	9873
rs139669483	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73110477	CAATTTATTGGTATA[C/T]AGTTGTTCATAGTAC	9873
rs139673303	snp	C/G	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:72869430	GGAAAGAGAGGGTTG[C/G]GGGGAGGGAAGAAGA	9873
rs139679700	in-del	-/AGG	0.0134861	0.0810011	intron-variant	FCHSD2	GRCh38.p7	11:72882418	GAAGGATTATGGGGA[-/AGG]AGAAGAAGAGAGATT	9873
rs139693098	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73138320	TGACTGCAGTGTCCA[C/T]ATTCTTGACCATAAG	9873
rs139716607	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014349	GCCCAGTCTAGTCTT[C/G]AACTACTTGCCTCAA	9873
rs139718830	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73104860	ACCGTGCCTGGCCAA[C/T]TTTACTAATTGAAAG	9873
rs139719199	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72951400	TGATAACACAGCAAA[C/T]GAGAGCGACAGATTA	9873
rs139724091	snp	C/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72959737	GGAGCAATAGAAGTA[C/T]TTAATATTAAATGTC	9873
rs139731234	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72952208	TTCTCTATCTTAATA[C/T]CAGAAAGATATATAT	9873
rs139731860	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73115489	TGAAAACAATCTTAT[A/G]TATCTTTTCCAACTC	9873
rs139732100	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73057581	ACATCTATATAAGGA[A/G]TATTCTACCTCCTTC	9873
rs139791467	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965896	TAAAACAGAACACAA[C/T]ACTGGAGGGGAAATG	9873
rs139836028	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73071122	TATTTTACAAGAACA[C/T]TTTTGGAAGACACAG	9873
rs139843152	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73077170	TCGTTCTACTTTCAC[A/G]TATGTTTGAAAACTT	9873
rs139844164	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72979823	AAGACATATAGGAAG[A/C]TCTCAGGATAAATAC	9873
rs139864836	in-del	-/C	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73114996	CAGCACAAAGACTTG[-/C]CTAAGAATTGGAGTC	9873
rs139877831	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72921726	AAATTTGTTCGTTAA[C/T]GCATTCTTCTAATAT	9873
rs139904240	in-del	-/A	0.0912534	0.193131	intron-variant	FCHSD2	GRCh38.p7	11:72979493	AACTTCTAAAAAAAG[-/A]AAAAAACAAACAATT	9873
rs139907370	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72859778	GCTAGGGCTAGAAGC[A/C]CTAAAAAGGATTAGG	9873
rs139932333	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099246	ATGAGGTACTACTTC[C/T]TACCCACTAGGATGG	9873
rs139942011	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73030923	TCTCTATACTTGCGC[A/G]TCCTGAATTTCTGCT	9873
rs139946654	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73045962	AAAAAACATCTCTTG[C/T]TTATATTTCTACAAT	9873
rs139952715	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73085472	GACTGAAATGACTTT[C/T]GGAGGATTTAAAGAA	9873
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	9873
rs139978371	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72944271	AATAAACATAATCCA[A/G]CATATAAACAGAACC	9873
rs139990700	snp	C/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72890543	GCTAGATCAAATGAT[C/G]ACCAAGGGTTTCTTC	9873
rs140047600	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047584	TGAAATAAAGTATTA[A/T]CCTATCAAATAACAT	9873
rs140054772	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73050454	TACTATAAACATATA[C/T]GGGACGGGTCACCTT	9873
rs140058120	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144139	TCCTCACTTGTAAAA[C/T]GGAGGTATAATGCTA	9873
rs140087490	snp	A/G	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72899417	TTAGTCATTAGGGAA[A/G]TGCAAACCAGAACCA	9873
rs140088581	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72998471	CACCTGAGCCCAAGA[A/G]GCAGAGGTTGCTGTG	9873
rs140101651	in-del	-/GAT			intron-variant	FCHSD2	GRCh38.p7	11:72846092	AGATAGATAGATAGA[-/GAT]TAAGTAGTTACGATT	9873
rs140103402	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73033856	TTAACAACTAGTATA[C/T]TGTATTTACCTATTT	9873
rs140132918	snp	G/T	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73090874	CCTCTAATTTCAAAC[G/T]TTTTCATCACCCCAG	9873
rs140144850	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73095181	CGAGTTAACTTTCCT[A/G]ACTGTGCTTCAGTTT	9873
rs140145201	snp	A/C	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:72934594	TTGCCTCGGCCTCCC[A/C]AAGTGCTGGGATCAC	9873
rs140145919	snp	A/C	0.0256215	0.110247	intron-variant	FCHSD2	GRCh38.p7	11:72906921	GGCTCTTTTTCGGTT[A/C]CATATGAACTTTAAA	9873
rs140146646	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73003926	AGCCTGGCCAACACG[C/G]TGAAATCCCGTCTCT	9873
rs140146837	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036785	GTCTTCCTCCACAAA[C/T]ATTGTGTTCACTCAT	9873
rs140147424	snp	C/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842427	AAGATGGAGGTGTGG[C/G]AGGATGGCCACATTC	9873
rs140147529	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72904015	TGCAAAGAATTTATA[A/C]TCTGGGAACTGGGCG	9873
rs140160021	snp	A/G	0.031825	0.122064	intron-variant	FCHSD2	GRCh38.p7	11:73009326	ACATGGTGAAACTCC[A/G]TCTCTACTAAAAATA	9873
rs140178229	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72849617	AGCCTAAACTCATCA[C/T]CATTCTGTTATGTTG	9873
rs140212338	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039722	TTCATTATCAAGGAT[A/G]ACGAATGATGCAGGA	9873
rs140212673	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853122	ATAACAAACCTGCAC[A/G]TGTACTCTTGCACTT	9873
rs140213795	snp	A/C	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72939922	CATGCCTGGCCTTGA[A/C]GGCTCTTTGTATAAC	9873
rs140228039	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73019847	AAAGGTTTACTTACA[C/T]AGAAAACAAAATCCA	9873
rs140230474	snp	C/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73112807	GCATACACTATCATG[C/T]CTGGCTAACATTTAT	9873
rs140250816	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862295	CCAAATAGGAAAGGA[A/G]TAAGTAAAACTGTCT	9873
rs140255342	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72961474	TTGCCCAGGCTGATA[C/T]TGAACTCCTGGCCTC	9873
rs140260667	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73026871	CGCTCTCTCTCCTGC[A/G]ACCATGTAAGACATG	9873
rs140262262	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72969327	TTTGGCTTTAAGTTA[C/T]TTATATCAGGAATAA	9873
rs140264980	snp	A/G	0.0170251	0.090679	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836522	TCCCATGGGAAAAGC[A/G]AAGACCGTAACCTAT	9873
rs140272859	snp	A/G	0.0228947	0.104514	intron-variant	FCHSD2	GRCh38.p7	11:73090295	CAGTGGCGGGATCTC[A/G]GCTCACTGCAAGCTC	9873
rs140280382	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72987222	TTAACTTCCCCTTCC[-/C]TGATCTTCCTCCTTA	9873
rs140283903	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72865769	GGAGTGGGAATCTCA[C/G]AGTCTTTTAATCTTT	9873
rs140324220	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72933735	TCTCAAAGCTTAAAG[C/T]AGACAATTTTTATGT	9873
rs140378749	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840680	CAGTGAAAAAAGTTC[C/T]AGTGTAGATTAAATG	9873
rs140380444	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038908	ATAAATTATGACATG[C/T]CTCCCACTTTAGTGT	9873
rs140380718	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73097848	ATATTTACTCTGTCT[A/G]TCTATTTTAGAGACA	9873
rs140386400	snp	A/G	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72860129	TGAGAATCTAATGCT[A/G]CCTGCTGGTCTGACA	9873
rs140389692	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72938766	CACAATTTTCATTAA[C/T]AGAATAGTTCAGTTC	9873
rs140393712	snp	C/T	0.000125276	0.00791343	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72889839	CTTACCCGTTGTTGG[C/T]GAACAATGTTTTTAT	9873
rs140405680	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72845386	GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG	9873
rs140445702	snp	A/G	0.0221141	0.102801	intron-variant	FCHSD2	GRCh38.p7	11:73124518	CCCAGCACTTTGGGA[A/G]GCCAAGGTAGGTGGA	9873
rs140484268	in-del	-/G	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72989910	AAGCTCAGCAAAGCA[-/G]GAGGAGACACTGGTG	9873
rs140486256	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994896	AAGTATACAATTCAG[C/T]GGTGACAAGGTTGTT	9873
rs140502810	snp	A/G	0.0279526	0.114869	intron-variant	FCHSD2	GRCh38.p7	11:73091943	AGGAGGCTGAGGCAG[A/G]AGAATTGTTTGTACC	9873
rs140511235	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72886355	CATAAGTCTGTGCTA[C/T]CCCCTTTTCTCTGAC	9873
rs140545626	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73118147	AACATGGTAACACCC[C/T]ATCTCTACTAAAAAT	9873
rs140551501	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73065613	TTAGAAAACCCCATC[A/G]TCTCAGTCCAAAATC	9873
rs140556226	snp	A/G	0.0134861	0.0810011	intron-variant	FCHSD2	GRCh38.p7	11:73063364	GAACATCAACACTAT[A/G]AAGAAACTGCATCAA	9873
rs140557765	snp	A/C/G	0.000305991	0.0123655	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867866	AAAAGAAATCGTACC[A/C/G]AGTGTAAAGTGCCAT	9873
rs140561459	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936068	ACTTTCATTCAAATC[C/T]CAGTTCTACCACTTA	9873
rs140568204	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73014900	CCAGGCTGGAGTGCA[C/G]TGACATGATTTCGGC	9873
rs140570012	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067702	CACAGAGAAAATGAG[C/T]GGAATGAAAAAAAAC	9873
rs140572677	snp	A/G	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:72970197	TTGAACAGATAATAC[A/G]TATACCACTTCCTTT	9873
rs140633743	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73017281	ACCAAACCTGGCCAA[C/T]GTATTACTTTTGGAT	9873
rs140695121	snp	A/C	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73062930	TCAAATTCAGGAAAT[A/C]CATAGAACACCACAA	9873
rs140697681	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016656	TGAAGTAGACAGATA[C/T]ATACTGGCATGTAAA	9873
rs140718366	snp	A/G	0.0130921	0.0798413	intron-variant	FCHSD2	GRCh38.p7	11:73107204	GGATTACAGGCATGC[A/G]CCACCATACCCAGCT	9873
rs140736128	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72872180	TTGGTAAATACTCTT[A/G]CAAAAATCTGCTTAT	9873
rs140747098	snp	A/C	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73016132	ACATGGTGAAAATCT[A/C]TCTCTACCAAAAATA	9873
rs140752948	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72954352	TAGCTGGGACCACAG[A/G]TGCATGCCACCATGC	9873
rs140771439	in-del	-/A	0.47726	0.104176	intron-variant	FCHSD2	GRCh38.p7	11:72897320	TTTTTTAAAAAGAGT[-/A]AAAAAAAAAAAAAAA	9873
rs140782014	snp	A/C	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:73064787	TCCTTGACACATACA[A/C]CCTCCGAAGTCTAAA	9873
rs140783978	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969453	AAACACTGAGAGGGA[A/C]AGAGACAAAAAGATG	9873
rs140817195	snp	A/G	0.0275645	0.114116	intron-variant	FCHSD2	GRCh38.p7	11:72914054	AGGAGTCTCACTGTC[A/G]CCCAGGCTAGAGTGC	9873
rs140830158	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101389	TAACTCTGTACTGAG[A/G]TGGGAACTACTGAGG	9873
rs140848228	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72912237	AAATCTTAGAGGAAA[C/T]GCATTCAGTTTTTCT	9873
rs140891884	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894053	TTTAACTCTGTAACT[A/G]AAATATAACCATTTC	9873
rs140926660	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73133367	GTAGAAACAACCCAT[A/G]TCTCTGTCAACTGAT	9873
rs140930483	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73081835	AACATATATAAAATA[C/T]TCAGAGCATGGTACA	9873
rs140940361	in-del	-/TTG	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:73041593	ATTTATGGAGTTTTT[-/TTG]TTTGTTTGTTTGCTA	9873
rs140968315	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72994436	GTAGCAGTGATCCCA[C/T]TAAGATGAGAAAATA	9873
rs140971021	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73091419	CCAGGTGTGGTGGTG[A/G]GTGCCTGTAATCCCA	9873
rs140985202	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73137163	TCATGAATACCAAGA[A/G]GAGGCAAGTTTCAAC	9873
rs140999225	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935280	TTTGATGTAATTTCC[C/T]CTAAAGTAAGAACTT	9873
rs141005370	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73068812	TCATCTCTACAAAAA[A/G]TAAAAAAAAAAAAAA	9873
rs141027363	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73135256	CACAGATACAGGGGA[C/G]AGTACAGTAGTATGG	9873
rs141040331	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73073401	CAACTTGAAAAAGTT[C/G]ACTGCTTGAATTCCT	9873
rs141046332	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73021085	GTCTCGCTATGTTGC[C/T]CAGGTTGATCTGAAC	9873
rs141105155	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72929384	TTACCACCTCTGCAA[A/G]GCTGTGATACTCATT	9873
rs141143422	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72895764	GCTAATTCTAAAACG[C/T]AACACTCATGTCTTT	9873
rs141144931	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138726	CAATTCTCTGCCTCA[A/G]CCTCCTGAGTAGCTA	9873
rs141145006	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087992	TCAAGTGATCCTCTC[A/C]CCTCAGCCTCTTAAA	9873
rs141187345	snp	A/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73044598	AAAGTCACTCATAAA[A/T]CTTAATTCTATTAAT	9873
rs141199608	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73102488	CTGAAAGCAATGAAA[C/T]GAAACATCCATCAAC	9873
rs141200549	snp	C/T	0.0232847	0.105357	intron-variant	FCHSD2	GRCh38.p7	11:72941304	TGAATTAATGAATGG[C/T]CTCAAATAAAAACCT	9873
rs141204574	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73042771	TTGTAGGTCTTTCAT[C/T]TCCTTGGTTAAATTT	9873
rs141223001	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135880	GGGGATTAAGGGGTG[C/T]GTTGCAGCAGTAGTG	9873
rs141231810	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73119781	TATACAATATTTGAC[C/G]CATCAATTCTACTTC	9873
rs141250039	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72888988	TTGAGACAGAGTCTC[A/G]CTGTCGCCCAGGTTG	9873
rs141266427	snp	C/T	0.0433465	0.140692	intron-variant	FCHSD2	GRCh38.p7	11:73068064	ACTTATTCACTACCA[C/T]GAGAACAGTATGGAA	9873
rs141275823	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892536	AATGTTCCAATACCA[A/C]CTTCACTATCAAAGA	9873
rs141289190	snp	A/G	0.000153988	0.00877327	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72989000	TCTCGTACTGCATGA[A/G]CCATCTGTTCAGTCT	9873
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	9873
rs141315742	snp	G/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73106778	TCAGTACAGTAACAT[G/T]CTGGACAGGTTTGTA	9873
rs141317479	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72948828	CCGCCACTACGCCTG[A/G]CTAATTTTTTATATT	9873
rs141380977	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73052493	TTAAAGGCTAATGCA[A/G]TGTATTAGAGAGTAC	9873
rs141383130	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72953821	GAGTATCGAGTTCTG[C/T]GGCTCTCTGGCATTA	9873
rs141394612	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73117312	GTGGAGAACTAAGAA[C/T]TCACAATCAGGCAAT	9873
rs141411173	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034401	ACAAACATGCAAAAA[C/T]GTTCCTCTTCCTGAA	9873
rs141420513	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73017069	CTCAATGCAGCCTCA[A/C]CTTCCTGGGCTCAAA	9873
rs141423275	snp	A/G	5.3934e-05	0.0051927	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73001122	AAAAGATTTCCAAAC[A/G]GGATACATGCTCCTA	9873
rs141441544	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72874602	TTAATTGCTGAAGCA[A/G]AAAAGAGAGAAGTAT	9873
rs141531486	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73104285	ACTTATTTATTTATG[C/G]AGACAGAGTCTCACT	9873
rs141551349	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72913216	TGATGAGATTTGGGT[A/G]GGGACACAAATCCAA	9873
rs141562392	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72951379	TATGACAAAACATCT[A/G]GCATATGATAACACA	9873
rs141571649	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72954222	TTTTTTTTTTTTTTT[-/TT]GAGACAGGGTCTCAC	9873
rs141591305	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73048971	GAGCTATGAAGAACA[A/G]TAAATATTTAAATAA	9873
rs141617677	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72943879	GTAAACTACTACACT[A/G]AGAACGTATGAAGAT	9873
rs141619117	snp	C/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73080696	CACCTGTAATCTCAG[C/T]ACTTTCGGAGGCTGA	9873
rs141677196	snp	A/C	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:73083568	AAAAGAAAAAAAAAA[A/C]AACAAGAAAGAAATA	9873
rs141698014	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73093476	TTCTCGAACTTACAG[C/G]TGGTGTCAGAATTGA	9873
rs141722119	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937664	TTTTTTTAGAACCTA[C/T]TCTGTGCCAAGAACT	9873
rs141729582	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73039238	AGAACCTAACTTTCT[A/G]CAGGGTGCAGTGCTC	9873
rs141731801	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73076766	AGCTATAAATGAACA[A/G]ATTTTGTAATGTATT	9873
rs141731947	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72924898	TATCAGGACATACTT[C/T]TCCTGAACTTGTTTA	9873
rs141734054	snp	A/C/G	0.00795819	0.0626103	intron-variant	FCHSD2	GRCh38.p7	11:73028840	AGCACTTCCCCTTTC[A/C/G]TTCTCTCCGTCTCTC	9873
rs141746971	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73030936	GCGTCCTGAATTTCT[A/G]CTATTTTTTATCCTT	9873
rs141759129	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034743	CTGCAAATTTTAAAG[C/T]AAAAGTAAATAGAGC	9873
rs141791908	snp	C/T	0.0158469	0.0875917	intron-variant	FCHSD2	GRCh38.p7	11:72933044	AGTGGCATCCTTTTA[C/T]GTGGAATTCCAAGAC	9873
rs141799406	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:72930262	TGCCGAAACAATCTG[C/T]TGTGACTCTAAGACT	9873
rs141804603	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72877587	AAAGTCTCTTAGAGA[C/T]ATATTTATTCTACAT	9873
rs141804665	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936921	AGTAAGTCCAATGTA[C/T]GGACTTCCTTGGAGA	9873
rs141811726	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72873044	ATTAATGTTACAAAT[A/C]TTAGGCCAGGCACGG	9873
rs141828520	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72983015	AATAAAAGAAAGGGG[C/T]CGGGCGCGGTGGCTC	9873
rs141849544	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73061951	CCCAGCACTGTGTTC[A/G]AGCTCTGTGAAGGGT	9873
rs141861044	snp	C/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72927137	TAGGCAAAAAACCCT[C/G]TAAGCCTTTAAGGGT	9873
rs141870443	snp	A/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72883111	TGTATAGGAAAAAAC[A/G]AAACAAAACAACAAC	9873
rs141878044	snp	C/T	0.0193772	0.0965046	intron-variant	FCHSD2	GRCh38.p7	11:72909181	GTCTGGGATTGCAGG[C/T]ACACGCCGCCACGCC	9873
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	9873
rs141942027	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72932561	GCCTCTGAGCTTTCA[C/T]ACAGGCTTTTCTTCT	9873
rs142022530	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73098968	CCTATAATCTCAACA[C/T]TTTGGGAGACTGAAG	9873
rs142040552	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73126902	AATTTGCCGAGCATC[A/G]TGTTGCACACCTGTA	9873
rs142059365	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036377	TACAATATTTCACAA[C/T]GTTATATCGGTCTTT	9873
rs142063236	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:72979950	GTAAGAACAGAATGT[C/T]CAGGAAATACGAAAA	9873
rs142064444	snp	A/G	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72880203	AAAGAAATTGAAGAG[A/G]ACAAAAACGAATCCA	9873
rs142066704	snp	A/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73055653	ATGTTACAAATATAT[A/G]TATCACTTAAATTTT	9873
rs142085324	snp	A/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72902728	TATTCTGCTATTTTC[A/T]ATACAAATGAGAAAT	9873
rs142104148	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73112617	TCCTCTTTAAGGTCA[A/G]TAACTCTTAGATTTG	9873
rs142130423	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73061270	GCCTGAAGAACTCTG[A/G]AACAGATACTGTGCT	9873
rs142135014	snp	A/G	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:73059259	CACTGTGTGAACTAC[A/G]GTTTATTTACCCTCC	9873
rs142144574	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73013478	CTAGCCTCTCTAATC[C/G]TAAGGTCTACTTTAA	9873
rs142155723	snp	C/T	0.0158469	0.0875917	intron-variant	FCHSD2	GRCh38.p7	11:73002331	ATTTAGGCAGAGGTG[C/T]ATCACTATTCCTTTG	9873
rs142166708	snp	A/G	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72971718	CCCCAGAATCTCCAG[A/G]TAAGAATGCAGCCAA	9873
rs142195604	in-del	-/C	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72856307	CAGGATATGATGAGT[-/C]CAAAAGTACAGGCTG	9873
rs142197813	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72854280	GATATTTGTAAACAA[A/G]TGTTCACAGCCACAT	9873
rs142199416	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72914556	ATAGACCAATGAAAC[A/G]GAATAGAGAACCCAG	9873
rs142233360	in-del	-/GA	0.115788	0.21092	intron-variant	FCHSD2	GRCh38.p7	11:72908343	TGCTGCAATCAACAT[-/GA]GAGTGCAGATATCTC	9873
rs142236923	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051352	TTTAAATCTGAGAAA[A/C]TGTAAGCATATTTTC	9873
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	9873
rs142265247	snp	C/T	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72852502	GAAACCTTGTCTCTA[C/T]TAAAAATACAAAAAT	9873
rs142266887	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947499	GGAATTGACCACAAG[A/G]TCTTATTCTAAGCAA	9873
rs142288080	in-del	-/GT			intron-variant	FCHSD2	GRCh38.p7	11:73088459	TGATTGTATACATAC[-/GT]GTGTGTGTGTGCGTT	9873
rs142302248	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858964	GGGATGGGAAACAAA[C/T]AAACTCCTACAACAT	9873
rs142335433	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72907887	CGTGAGCCACCATGC[C/T]TGGCTGGTTTTGTTA	9873
rs142372915	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73096423	AGATGTGGTGGCGGG[C/T]GCCTGTAATTCCAGC	9873
rs142380262	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041087	ATGGCTAAATAGTAT[A/T]CCATTGTGTATATAA	9873
rs142394697	snp	A/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73033301	TCAAAAAAAAAAAAA[A/T]AGTAGTTAGACTACA	9873
rs142402738	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940537	GAGCTATGGAGAAAG[A/G/T]AGTAGTCTCATGTCA	9873
rs142409479	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72885567	GAGGTTTCGTGGAGT[C/T]AGGGTACCAGTCGGT	9873
rs142433632	in-del	-/TATA			intron-variant	FCHSD2	GRCh38.p7	11:72980676	GTATGTGTGTGTGTG[-/TATA]TATATATATATATAT	9873
rs142448157	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72873599	ATGATGTCTAATTTA[C/T]CTAGTTTTTCTTTTG	9873
rs142464402	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73124030	GTCCATCAATGATAG[A/G]CTGGATTAAGAAAAT	9873
rs142485523	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085096	TAAGATCTTACTATA[C/G/T]TTGTTTTGAGTAAAT	9873
rs142521777	snp	A/T	0.0221141	0.102801	intron-variant	FCHSD2	GRCh38.p7	11:73064237	TGTTCTTTGAAACCA[A/T]TGAGAACAAAGACAC	9873
rs142558696	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131219	AAATCCCATCTCTAT[A/G]AAAACTACAAAAATT	9873
rs142558957	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:72979089	TCTCAAACTCCTGAC[C/T]TCAGGTGATCTGCCC	9873
rs142568333	snp	G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73082730	CATATTTTAAAATTT[G/T]TGCTACAAAGACAAC	9873
rs142568897	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72881146	CAAGGGACTAATATA[A/C]GGAATATACACGGAA	9873
rs142587978	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981105	GAGTTTTCCTGTACT[A/G]CAGACTATAGAATTA	9873
rs142618697	snp	A/C	0.000148318	0.00861028	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72887556	CAGCAGCTCCATGAC[A/C]CTCCAGATCATTTAG	9873
rs142620764	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024844	AGGACATGAACAGAC[A/G]CTTTTCAAAAACAGA	9873
rs142620849	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72921261	AAACATTTTAATCTA[A/T]CAAATCTTGAAGAAA	9873
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	9873
rs142629561	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72989901	GACTGGCAAAAGCTC[A/G]GCAAAGCAGGAGGAG	9873
rs142637835	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72927449	TGTGCCACTCTGATG[A/G]GGGATGTTGATAGTG	9873
rs142660548	snp	G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72864850	ACAGGCTGATGGGGT[G/T]GCTGGCAGCAATCTA	9873
rs142693354	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72997470	TCCAATATTGTGAGT[C/T]ATAATCAAACAGAAG	9873
rs142695604	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73094167	AATGAGCCAAGACCA[C/T]GCCAATGCACTCCAG	9873
rs142700060	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002666	GGAGATACCCTTCAT[C/T]CATGTTCTTCTCTCA	9873
rs142702801	snp	C/T	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:72939649	TTTGAGACAGTGTCT[C/T]GCCCTGTCGCCCAGG	9873
rs142724039	snp	C/T	0.000141794	0.00841883	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840843	AATTTGGAAGAACTA[C/T]GCATTCGATAATCCT	9873
rs142729788	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73007387	GCATTTTGGGAGGCT[A/G]AGGCAGAAGGATTGC	9873
rs142730356	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848513	CTATAAATCTTTTCA[C/T]ACTTGTTCTATTTTC	9873
rs142736469	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72943054	TGGAGTGCAATGGTG[C/T]GATCTTGGCTCACTA	9873
rs142767971	in-del	-/AA			intron-variant	FCHSD2	GRCh38.p7	11:72851102	CGTGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA	9873
rs142861333	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73059730	TCTTTCTTTTTTTTT[C/T]TTTTTTTCCCCTAGC	9873
rs142891668	snp	A/C	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73138096	ATCAGCAATAATACA[A/C]ACTAAGCAACAGCAA	9873
rs142899648	snp	C/T	0.000284542	0.0119243	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867911	GGAGGGCGGGCCCAT[C/T]GCTCATTTTCCAGTT	9873
rs142906284	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73123533	TGTAAAGTGCACAGG[C/T]GACTCTTGCTTTTAT	9873
rs142916551	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72854768	GACAGAAAGCAGAAT[A/G]GTGATTGTCAGAGGC	9873
rs142924895	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72934725	TATAAATGTGAGTTA[A/G]TCTGGCAGTATGAAC	9873
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	9873
rs142951785	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108057	GAGGGTCCCCTTTTC[A/T]CCACATCCTTGCCGG	9873
rs142964299	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72955042	CAAGCAATTCCCTGG[A/C]AGATACCAGCTGGAC	9873
rs142964390	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73054970	ATACTTGAGACTGGG[C/T]AGTTTATAAAAAGAG	9873
rs143009366	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73074188	CAAAATATCACTTCA[A/G]TACAGTGCTGGAGTG	9873
rs143029589	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903621	ACATACCTTGGGAAA[C/G/T]AGTGGAAATCGGCAT	9873
rs143031441	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962259	ACAAGTATGTGGTAT[A/G]GTTTTCTAGAGGCTG	9873
rs143081503	snp	C/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73021504	TAAATGGGAGCTAAA[C/T]GATGAGAACACATGA	9873
rs143086970	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72931271	TTTTTTTTTTTTTTT[-/T]AGTAGAGATGAGGTT	9873
rs143099261	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960419	TAGTCTGCTGCTCCT[C/T]TGGATTTAAATGGAT	9873
rs143129014	in-del	-/TTG			intron-variant	FCHSD2	GRCh38.p7	11:73100335	GCGCTTTACATGCTT[-/TTG]TTGTTGTTGTTGTTG	9873
rs143131200	snp	C/T	0.0295035	0.117819	intron-variant	FCHSD2	GRCh38.p7	11:72906385	TAGGGTGCCTGTTCA[C/T]TCTGATGATAGTTTC	9873
rs143143356	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72888134	CAAGATAGCCAAGTA[C/T]AGGAATCTGAGAAAC	9873
rs143180594	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019545	CAAAGCTAAACTGTA[C/T]TAAACTGAATGAGCC	9873
rs143191185	snp	C/T	0.00769574	0.061552	intron-variant	FCHSD2	GRCh38.p7	11:73077705	AATGAAATACTGATG[C/T]ACACAACAACATAAA	9873
rs143215833	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087513	GAGTTTGAGACCAGT[C/G]TGCCAACATGGTGAA	9873
rs143233093	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73137424	TAATTAAAGTGATCA[C/T]GTGAACCAAAGTATA	9873
rs143233886	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72922409	GTGACAGAAAAAACA[C/T]AATAGAAATATTAAA	9873
rs143247683	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033612	AAGCAACTACAAGCA[C/T]ATCCACACTCCCAAA	9873
rs143255561	in-del	-/AG	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73007627	AAGAAGAAAGAAAAA[-/AG]GGGGGAAAAAGAGAA	9873
rs143283322	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066254	CAATGGGGAAAAGAT[G/T]ACCTATTTAATAAAT	9873
rs143308827	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72874188	CTAGCACCATTGTAG[C/T]ATGCTTTTGCTTTTT	9873
rs143309417	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73025732	AATCTGTATACTTGT[A/G]ACTAAACTATATCTC	9873
rs143353128	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928544	AACACAGGCAACTGA[C/T]ATTTACTAACGGCTT	9873
rs143353518	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73027710	TCGCTGCACTCCCCG[C/T]CATCACAGGCCCAGG	9873
rs143355152	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72865213	CCTCTAGAATGTGCA[C/T]TTCTGCTTCATGTTC	9873
rs143382984	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73117662	GGGAATGGGAAGAAA[C/G]CTTCAACAGATTATT	9873
rs143395790	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73103869	CATGAACCAAGCAAA[C/T]TCTCCTCCAGAGAAG	9873
rs143406067	in-del	-/C	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:73020679	GTAAGATTAAAAAAA[-/C]AGTATATTATTTTAA	9873
rs143407520	snp	A/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72969477	AAAGATGAATCTTTG[A/T]CTTAATTTTTTGAGG	9873
rs143408886	snp	A/T	1.64765e-05	0.00287019	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843514	GTTCCTCAATGGTCA[A/T]CTCATCTGGTTGAGA	9873
rs143410428	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72867042	AGAGAACCAGGAAGA[C/T]ATGGCAATTACATTC	9873
rs143414149	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011382	GAACATGTGCACCAC[C/T]TAGGCTAGCAGGTGG	9873
rs143430107	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048497	TAAATGCTAACTTCT[A/G]CTCATGAATCTGCAG	9873
rs143430419	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:72991662	CAACGACAAAAACCA[C/T]ATGATTATCTCAATA	9873
rs143436453	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73140990	CAGACACGGGTGAGT[C/T]AGGCGTTAGGCAAAT	9873
rs143461020	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889736	ACAAAACAACACATA[C/T]AGGATATTTTTCACA	9873
rs143474930	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72895536	TCACAAGCTAGATAG[A/G]GGAACTTTCAGGCTC	9873
rs143495237	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72996612	ATACAATTGTGTTTA[C/T]CTTCCAAGCATTATA	9873
rs143501492	snp	G/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140420	CAAGCTCAATCCACG[G/T]CTAGGTCTTCCTACA	9873
rs143514898	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72911765	TTTGTTGCCTAGGCT[A/G]GAGTGCACTGGCACA	9873
rs143515808	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73015688	TTTTGAAATTATATC[C/T]GAAAACACAGCAGAG	9873
rs143537137	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73047680	TGGGATTAGAACCCC[C/T]TTCTCTTTTCCTTTC	9873
rs143543601	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840467	AATAATATATTCACC[C/T]GGAGAATAAACGCTC	9873
rs143544414	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:73138381	AAAATGGAGACAAAA[C/T]GCAATCAAGAAGTCT	9873
rs143548146	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855949	AAAAACCTAATAAAG[A/G]AGAGACAAACAGCCT	9873
rs143553457	snp	A/C	0.00755907	0.0610114	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840119	CCTATATCCTTTCTG[A/C]CACCCTCCATCCATC	9873
rs143563717	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72937446	TTCAGTAAACAATAT[C/T]TCTGATGCTGGCCAA	9873
rs143606848	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72994617	AAAAATACAAAAAAA[C/T]TAGCTGGGTGTGGTG	9873
rs143606909	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73050666	CCATATCCACATGGG[A/G]AGATAATGGGAACAT	9873
rs143635163	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73038445	CAGATCAAGAAAAAT[A/G]GGCAGTGACTCAAGA	9873
rs143652784	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115514	CAACTCTATACTTTC[A/G]TGTCGTTTTCATGTC	9873
rs143654667	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73009365	AGCCAGGTGTGGTGG[-/C]CGTACACCTGTAATC	9873
rs143658197	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72847226	TGGTCTCAAACTCCC[A/G]GCTTCAAGTGATCTT	9873
rs143659152	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72899521	GAGGATCTTTTGAGC[C/T]CAGGAGTTCAAGGCC	9873
rs143659400	snp	G/T	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72882482	GATAAGTTCTGGTGT[G/T]TGATAGCTTAGCAGG	9873
rs143659748	snp	A/G	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:72844440	AGACTGAGCTGATCC[A/G]TTTGCGTGCTACCGT	9873
rs143663537	snp	C/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:72982697	AACTGTAATCTAATC[C/T]ATCTGCATTTCAGAG	9873
rs143672859	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144258	CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT	9873
rs143701055	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114943	GGTGTCTCACTAGGT[C/T]ATGTGCCCCACCATG	9873
rs143725899	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72998837	GATGTTGGCAAGGCT[A/G]TAGAGAAATTGGAGC	9873
rs143760818	snp	A/G	0.000555104	0.0166506	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72921844	TTGCTGGAGTTTTCT[A/G]ATAAAAACTGGAATG	9873
rs143769564	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73118819	CCATTTCTGTTTTAC[A/G]GATGAGAAAATTGAA	9873
rs143776225	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72904547	CCACCCCTAATTATA[C/T]TGAAACAAGTTCCAG	9873
rs143776544	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72975091	TTCTGTTCCTGGCTT[A/C]TTTCACTTAACATAA	9873
rs143787937	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73115377	TTTAGCAGAGATGGG[A/G]TTTCACTGTGTTAGC	9873
rs143807686	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73072247	TTGGGGAGGAAAATA[A/C]TGGGGATCAGCATCA	9873
rs143824289	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022880	GAGAGATCCCAGAAA[C/T]AGACCCATACAAATA	9873
rs143837769	snp	C/G	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72917205	GGCCAGGCTGGTCTT[C/G]AACTCCTGATCTCAT	9873
rs143839705	snp	C/T	0.0130921	0.0798413	intron-variant	FCHSD2	GRCh38.p7	11:72850124	GCTGGACTGCAATGG[C/T]GTGATCTTGGCTCAC	9873
rs143844192	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73054741	AGTGCAGTGGCACAA[C/T]CATGGCTCACTGCAG	9873
rs143850216	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73118387	GTTTCCTCATGCCCC[A/G]TCTTAGTCAATTCCT	9873
rs143851916	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72950821	CTATTTGTTGTTGTC[C/T]GCCAAATGTTATCCC	9873
rs143858039	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73090195	AATGTTTACAAATAT[A/G]TATTTATGGTAATTA	9873
rs143872333	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72864107	CATACTCTAAGTGAG[A/G]CTGTACAACAGAGTA	9873
rs143899766	snp	C/T	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72970733	ATGCGAATTCTTCTA[C/T]GAAGAAAAGACTTCC	9873
rs143940649	in-del	-/AG	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:72955621	TTCAGGAGCCCACTA[-/AG]AGTTACTTCATTAAG	9873
rs143942598	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933536	TTGGGTCATTGTTAT[C/T]TGCAATCAAAAGACT	9873
rs143957676	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73027033	GGAAATGGAGTAATA[C/T]AGAAAATTGGTACCG	9873
rs143959801	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73116851	CCATATCTCTTTTTT[C/T]AGTTATGAACTCAAA	9873
rs143979928	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879592	ACCACATAGAACTTA[C/T]AGAGCTAAAAATATA	9873
rs143999158	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73120008	CAAGTCCCCTCTTAC[A/G]TGGATGGCAGAAGGC	9873
rs143999802	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969394	ATTTAGGTTTTGCCA[C/T]CTCAGTTAATTTTTT	9873
rs144001366	in-del	-/C	0.0235167	0.105855	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836507	GTATTTCTTTTTTTT[-/C]CCCATGGGAAAAGCA	9873
rs144027695	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72871538	TCCACTTACTTAACC[G/T]AAGTAAAGTTCCACT	9873
rs144064911	in-del	-/A	0.236724	0.249647	intron-variant	FCHSD2	GRCh38.p7	11:73099281	AAAACAACACAAAAC[-/A]AAACAAAAACAGAAA	9873
rs144136190	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119508	CTCACTCTGTCACCT[A/G]AACTGGAAGGCAGTG	9873
rs144150140	snp	A/C	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:73105665	CATAAAGAACTCAAT[A/C]AATATTTATTATTAG	9873
rs144157976	in-del	-/AAT			intron-variant	FCHSD2	GRCh38.p7	11:73075426	TCAGAAACAACAGAC[-/AAT]GACAGGTATTTGCTA	9873
rs144182747	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73097180	GCTGATTTTTGTATT[C/T]TTTCGTAGAGATGGG	9873
rs144183464	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72971294	AGGAATAAATTTAAC[A/G]AAATACGTGAAGACT	9873
rs144196683	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72934146	AAAAGAGCTATTTAA[A/G]GCTTACAACAAATCA	9873
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	9873
rs144205568	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941109	GTTCCACTGTTACCA[C/T]TAATATAAGTAAAGT	9873
rs144291169	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143363	CAGGAGAGGCCATAG[A/G]GGAAGCCCTTGTCTG	9873
rs144311226	snp	C/G/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73016964	AATGTATTATGTTTG[C/G/T]TTTTTTGCTTGTTTG	9873
rs144320130	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72998415	GGTGTGGTGGCACAC[A/G]CCTGTAATCCCAGCC	9873
rs144322316	snp	A/C	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73095972	CTGTAAATTTGAAAG[A/C]CACAACCCTGAGCTA	9873
rs144333124	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73047367	GCATCTTATTCAAGG[C/T]TATAAGAAAAAAATA	9873
rs144333577	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72857883	TGAGGTAGAAAGCAG[A/G]GTCTTGGGGTCTGGC	9873
rs144344315	snp	C/T	0.000495878	0.0157383	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902551	CCCTTACAGTATCAC[C/T]GTCACAAGGCTGGAA	9873
rs144381133	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891995	TTCCTAGGTTCTTAA[G/T]AGCCTAAACAATGAA	9873
rs144393014	snp	C/G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72951481	GCACTTACTACAAGG[C/G/T]TTGGCATTTAGCTCA	9873
rs144407351	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72898046	ATGAGACAGCTATTA[A/C]GTTACTACATAAGAA	9873
rs144427542	snp	C/T	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:73015069	GGCTGGTCTTGAACT[C/T]CTGATCTCAGGTGAT	9873
rs144435093	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106050	AACTGGGATGAACTT[C/T]AGAAATTATGTGGAG	9873
rs144453070	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72848538	ATTTTCCAGTTTAAT[A/G]TTTAACCCTTCATAG	9873
rs144457320	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73131792	GCTAAGAAAAAAATG[C/T]TGCCAATTAACACAA	9873
rs144479618	snp	C/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72855554	CTTAATGCCACTAAA[C/T]TTACACTTAAAGTGG	9873
rs144488482	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72984381	TTCATCACTACTAAG[C/G]AATGAAACAGTGACT	9873
rs144510546	in-del	-/T	0.0629771	0.165899	intron-variant	FCHSD2	GRCh38.p7	11:73059720	GTGAGGTTTTCTTTC[-/T]CTTTTTTTTTCTTTT	9873
rs144520810	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928566	TAACGGCTTACTGAG[A/T]TCCAAGTGCTTTACA	9873
rs144550444	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73109856	AATGGCTTTTATTGT[A/G]TTGAGGTATGTTCCT	9873
rs144552217	snp	A/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72953522	ATCAATTTCAACCAC[A/T]TGAATTTATTGAACA	9873
rs144561750	snp	C/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73016259	AGTGAGCCGAGACTG[C/G]GCCTCAGCACTCCAG	9873
rs144581326	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73057880	TGCCAATTCGGTATT[-/C]TTTTTTTTTTTTTTT	9873
rs144605758	snp	C/T	0.0185938	0.0946107	intron-variant	FCHSD2	GRCh38.p7	11:72856529	AAAGGGAAAAGATTA[C/T]ACAGAATTGTGGAGA	9873
rs144606913	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72916004	TCTCATTTGTAAGTG[A/G]GAGCTAAATTATGAG	9873
rs144621421	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057279	TAGGACACAGTACAC[A/G]GGTTCGAAGCATGGG	9873
rs144631789	snp	A/G	0.000370934	0.0136136	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72868025	GCTTTCAATTTAATT[A/G]TCTAGAGAACCAAGA	9873
rs144641029	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72861475	AGACGAAATTCCATA[C/T]AATTCTACACAAGGC	9873
rs144649889	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72920967	TACAAGAGGCATTCA[A/G]GATGAAGAGTCTGTG	9873
rs144659156	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72872281	CACAACTTTTTTTTT[-/C]TTTTCTTTTTTTTTT	9873
rs144749100	snp	G/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73135407	AATAATTTTTCCATA[G/T]TATAGACCTCCTTAA	9873
rs144756868	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061276	AGAACTCTGGAACAG[A/G]TACTGTGCTTGTCGC	9873
rs144757924	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72964325	TGCACTGGCTCTTCC[C/G]TTTGCTTAAGATGTC	9873
rs144765007	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908912	GCCCACCTTGGCCTC[C/G]TACAGTGCTGGGATT	9873
rs144772331	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73129226	CAAATTACAGCTGGG[C/T]GCCATAATTTGTGAA	9873
rs144772849	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046759	TTTGTTTATTGATTG[A/G]TTGATTAAGACAGGG	9873
rs144784879	snp	C/T	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:73133664	AGCTGGGTACGGTGG[C/T]GGGCACCTATAATCC	9873
rs144798246	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72989940	GAAGGACTATTGTGC[A/C]AGGGTGAATAGTGTG	9873
rs144799677	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137541	ATAGCCAGTTACATT[C/T]GACAACAAGGGTATA	9873
rs144832332	snp	C/T	0.0244538	0.107838	intron-variant	FCHSD2	GRCh38.p7	11:72993872	TGTAACTAACCTGCA[C/T]GTTGTGCACATGTAC	9873
rs144842254	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72987380	CACATTACTACTGCA[A/G]GTAAGTTATTAGTTA	9873
rs144846314	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085797	CTGGTTCAAGTTGAT[A/G]TTTAAAAAAAAATGA	9873
rs144867398	in-del	-/TAACA	0.0479149	0.147179	intron-variant	FCHSD2	GRCh38.p7	11:73106626	GATAAATAAATACAG[-/TAACA]TAACATTTCCATAAA	9873
rs144868637	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73088473	CGTGTGTGTGTGTGC[A/G]TTTGTGTGTGTGTAC	9873
rs144868987	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72866419	GGATTATGGGCGTCT[A/G]CCACCATGCCTGGCT	9873
rs144913712	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72932732	GTGATATTTGTTTGT[A/G]TGTCCCTCTTTTTGT	9873
rs144917152	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994953	AACATTTTCCTACCC[C/T]AAAAAGAAACTCTGT	9873
rs144933882	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73092847	CCCAAAGACAGGTCT[A/T]ACCTTTGTCTTTGGC	9873
rs144939458	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988672	CATAGCAGTGACTTC[A/C]GGCTTTTGATAAGCT	9873
rs144947548	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73019095	TCTGGTATTTTCTCA[A/G]ATCACATCTAAATGA	9873
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	9873
rs144955256	snp	C/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72993772	GTGGGGTGAGGGGAG[C/G]GGGGAGGGATAGCAT	9873
rs144955525	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73110677	AATTTATTTCTGCTC[C/T]GATCTTTATTATTTC	9873
rs144959029	snp	C/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72929785	ACAAACTCCCCATCA[C/G]AGTATTTAAAACACT	9873
rs144974943	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860327	AACAATAGCAAAATA[C/T]ACATTCTTTTTTTTA	9873
rs144987216	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72960011	ACACATATTAATATA[A/G]GGTATTAATCTGTTC	9873
rs144987798	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72892943	ATATTAGCAGTGGTC[A/G]ATTCTAACAAAGAAA	9873
rs144998272	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72914982	CTACAGAATGGGAAT[-/TT]TTTTTTTTTTTTTTT	9873
rs145020567	snp	C/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73097943	CCTCCAACTGGCTAG[C/G]ACTAGACTTGCATAG	9873
rs145036173	snp	C/G	0.00239393	0.0345281	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839003	GAAATGTTGTGAGCA[C/G]GTGCTTTCAACCTAG	9873
rs145068964	snp	C/T	0.000444148	0.0148955	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72989037	ATTTCTTTTTGCCTT[C/T]AGCTAAATCTTTCAC	9873
rs145148955	snp	C/T	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:72905726	AGTTTGCTTAGAATA[C/T]TGGTTTCCAACTTCA	9873
rs145150639	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73060304	ATCTTCATTTCTACC[C/T]ATTTATTATTATTAT	9873
rs145182565	snp	A/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73065010	TAACTCCTTTCATGA[A/G]GCCAGCATCATCCTG	9873
rs145182795	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106986	CAGATATCCTGGACT[C/T]GACTTTTTAAAGCCC	9873
rs145194022	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73110624	TCACAAAACCAACTT[C/T]TCATTTTGTTGGTCT	9873
rs145197131	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72961616	TTGAGAAATGAATCT[A/G]AAGTGACTTGAAGAC	9873
rs145240004	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72959968	TTTTAAAAGCACAGA[C/T]ATATAGGAAGAAACC	9873
rs145240576	in-del	-/TTGTTG			intron-variant	FCHSD2	GRCh38.p7	11:72961406	TTTTTAAGAAGTTTT[-/TTGTTG]TTGTTGTTGTTGTTG	9873
rs145243066	snp	A/G	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:72862365	ATTTACAAAAAAGCT[A/G]CTAGAACTAATAAGT	9873
rs145244617	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73087007	TCCTACAGCTAACTG[C/T]AAAACAGCCTCAGGC	9873
rs145245706	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72988095	TCTTGTGAATAAAAA[A/C]TGTATTAGAAAGATA	9873
rs145253354	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:72866007	CAAAGTTAGATGGTA[C/T]GTGCCTGCTCAGTTC	9873
rs145279206	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72966548	TGCATAGCTTCACTG[C/G]AAGCTCCCTGCAAAG	9873
rs145316351	snp	C/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:73062933	AATTCAGGAAATACA[C/T]AGAACACCACAAAGA	9873
rs145337870	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72859914	AGTAAGGATACAGAA[C/T]AGCTGTCCCCAATCT	9873
rs145346308	in-del	-/TTTCTATTTT	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73097672	ACTTGTTATTGAGAA[-/TTTCTATTTT]TTTCTGTAATCAGTT	9873
rs145360918	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842151	GTGATGAACTAAGTC[G/T]AGGGTCACTTGAGTG	9873
rs145393765	in-del	-/AAGG	0.281049	0.248064	intron-variant	FCHSD2	GRCh38.p7	11:73103219	AAACTCTGTACACTT[-/AAGG]TAGATGGATTTTATT	9873
rs145399490	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940189	CTTAGCCTTTTAAAC[G/T]CATCACTACTGAGAT	9873
rs145405823	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73078994	CAAGTGTTGGGATTA[C/T]AGGCGTGCGCTACCG	9873
rs145412933	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73027047	ACAGAAAATTGGTAC[C/T]GAGAGACATGGCGTA	9873
rs145457810	in-del	-/ATA	0.349452	0.229367	intron-variant	FCHSD2	GRCh38.p7	11:73039925	TTAATATTCATGAGG[-/ATA]ATATCACAAAAGCAG	9873
rs145484225	in-del	-/GTTT			intron-variant	FCHSD2	GRCh38.p7	11:73016989	TGTTTGTTTTCGTTC[-/GTTT]GTTTGTTTGAGACAA	9873
rs145491476	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73086829	TGTCCCAGAAATGAA[C/T]AGATAAATACAATGT	9873
rs145506517	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72864130	CAGAGTAGACTGGCA[-/G]GTTTGCCCTTGCACA	9873
rs145516428	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72968276	ATAAATAACACTGGT[A/G]CTCTGTCCTTAAGAC	9873
rs145537418	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73039166	AGTCTAGTTCAAGAC[C/T]GTCTCACTGGGAGTA	9873
rs145550076	snp	G/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:72911279	TTCTTGACAACTTTG[G/T]CAAAAATGAGTTCAC	9873
rs145569785	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036939	ACGTTCATCTGTTAA[C/T]GCGGATCTGTAATTA	9873
rs145578424	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048209	GCAGCAGGATATTTC[C/T]GTATATCCTGTTTAG	9873
rs145586672	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73139146	TGAAACTAAAATCTT[C/T]GGGCTATAAACAGCA	9873
rs145594238	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72999311	TTGAATCTTACCAAA[-/G]ATTCTTTTTTTTTTT	9873
rs145603882	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73042794	TTAAATTTATTCCTA[A/G]GAATTTTACTTTTTT	9873
rs145608151	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72983017	TAAAAGAAAGGGGCC[A/G]GGCGCGGTGGCTCAT	9873
rs145608310	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134198	TCTCAGCACCATGCA[C/T]AGTGGCTCATGCCTG	9873
rs145624750	snp	A/C	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72880510	AAGGACACCCTCTTC[A/C]ATAAATGCTGCTGGG	9873
rs145635734	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839414	AGGTAACAACTGGAG[A/G]AAGGATCAGAGGCAA	9873
rs145687923	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040134	ATAATGTTACACAAA[A/G]GCTGAGTTCATTTGT	9873
rs145694213	snp	C/G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72953155	CTAACAGTGCTGGAT[C/G/T]AGAAAGAAAAGGTAT	9873
rs145694404	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73050722	TTTATATTGGTTGAA[C/T]GTTATGTCTCCATTC	9873
rs145736647	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73141056	CACCCAGTGCCCAGA[A/G]TAGACATTCAGTATC	9873
rs145750701	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72935690	AAATATCTTAATATG[C/T]AGTTGAATTTATCAG	9873
rs145752852	snp	C/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72899623	TCAGCTGTAGTCCCA[C/G]TTACTCGGGAAGCTG	9873
rs145761048	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73038002	TCTGATGAAAAGATT[C/G]ACCAAGTCAAGCTTT	9873
rs145788634	in-del	-/A	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73120031	AGAAGGCAAAGAGGG[-/A]AATGAGGAAGATGCA	9873
rs145823087	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72890895	TTGAGATAATTAGGA[A/G]TTTTTTTTAAAATAT	9873
rs145851714	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73053775	ATGACAAAAAAGTTA[C/T]GACTATAGCAGCGAT	9873
rs145860739	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73031673	TATTAACCAACACTG[C/T]TTATACCCAGGAATC	9873
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	9873
rs145881197	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73016820	GCCCACTTACTATTA[C/T]CTACACAACACAAAT	9873
rs145885705	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73107397	CAGGTGTATATATAG[A/T]TGAGGACATGAGATA	9873
rs145886931	snp	C/G/T			intron-variant	FCHSD2	GRCh38.p7	11:72872743	CTATTATGAATAATA[C/G/T]TGCTATAAACGTGTG	9873
rs145901429	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72902746	ACAAATGAGAAATCA[C/T]CCAACACTGTGGTAA	9873
rs145918758	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73020143	ACTTTTAAAAAGCCA[G/T]CAGTGTCTGATGTTA	9873
rs145919003	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72954927	CTGGCTGTATGTATA[C/T]GTAATAAAGATAGGA	9873
rs145933818	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72910386	GTTTTGTCGAAAAGA[A/G]AAGGGGGAAATGTGG	9873
rs145966742	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73126016	TGACATTAGGCAAGA[C/T]TCTATCTAATATGTT	9873
rs145970097	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73077042	ATGAACCCGGGAGGC[A/G]GAGCTTACAGTGAGA	9873
rs145970411	snp	A/T	0.029116	0.117091	intron-variant	FCHSD2	GRCh38.p7	11:73131336	TCCTGGCTAACACGG[A/T]GAAACCCCCTCTCTA	9873
rs145971576	in-del	-/AAATTAAA			intron-variant	FCHSD2	GRCh38.p7	11:73024159	ACTCTTAATATACGT[-/AAATTAAA]AAATTAAAAAAAATC	9873
rs145974150	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72956839	GAAAAAAAAAAAAAA[A/C]CAACCCTAGAAGACA	9873
rs145978076	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72852752	ATCAACCTAAATACT[A/G]ATCAATGACAAGTTG	9873
rs145981476	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72979320	AGAAGTCTCCCAAAA[A/C]GTACAACATAATGAC	9873
rs145985107	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72921552	GTAGAATACAAAACT[A/G]TTTAAACCCTTCTCA	9873
rs145985507	snp	A/G	0.000357782	0.0133702	intron-variant	FCHSD2	GRCh38.p7	11:72983849	TAACAAATGTTTGCC[A/G]CACCTAGGGAATAAT	9873
rs145989160	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73082967	GTAAAATTAAAGAAG[A/G]AAATGCTTCAATTTC	9873
rs145997556	snp	A/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72948200	TTTAGTAGAGATGGG[A/G]TTTTGCCATGTTGGC	9873
rs146004687	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72928100	CTTTAAAATCATCAA[A/T]GCATTGGCCACATAT	9873
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	9873
rs146033070	in-del	-/TACTT	0.0486741	0.148216	intron-variant	FCHSD2	GRCh38.p7	11:73098409	TATGGGTAAAGAAAA[-/TACTT]TATATGATTTTGATC	9873
rs146053285	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72939638	TTTTTTTTTTTTTTG[A/G]GACAGTGTCTCGCCC	9873
rs146056703	snp	A/G	0.000489345	0.0156344	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867923	CATCGCTCATTTTCC[A/G]GTTCTTCCATTACTT	9873
rs146072965	in-del	-/A	0.0444908	0.142359	intron-variant	FCHSD2	GRCh38.p7	11:72950010	TTTACATTCTCACCC[-/A]AATTTCTCCATCTCC	9873
rs146092192	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108356	CCCATTCTGTGGGTT[A/C]TCTCTTCACTTTGTT	9873
rs146092450	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73050040	GTTGCCAGGCCTCTC[G/T]ATATAAGAAGTCAGT	9873
rs146103224	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72951987	TCTACATATTGTTGG[C/T]ATTTTCAACAGGCAC	9873
rs146107435	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955250	GTTTGCTATAGTGGG[C/T]CACAGAACCCAAGGA	9873
rs146111778	snp	G/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73055424	TGGCAGAGCTGCCAC[G/T]TTCTACCCATACAGA	9873
rs146161580	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908292	ATCTGTTGATGGACA[C/T]TTAGGTTGCTTCTAA	9873
rs146171949	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:73096402	AAAAAAAAAAAAAAA[-/TT]AGCCAGATGTGGTGG	9873
rs146214858	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73031059	TCCTGCTATTTGTCA[C/T]AACATGTATGAATCT	9873
rs146233135	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73034782	TTACTTATTAAGGAT[C/T]AGGTGAATTTTGACC	9873
rs146233722	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73125288	TTTAAAGAAAACTAA[C/G]ATTATATTACGAGGT	9873
rs146250321	snp	C/T	0.143622	0.226238	intron-variant	FCHSD2	GRCh38.p7	11:72878881	GGAGGCCGAGGCGGG[C/T]AGATCACTTGAGGTC	9873
rs146313546	snp	A/C	0.00835141	0.0640778	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144402	TGCCTGTAGTCCCAG[A/C]TACTCAGGAGGCTGA	9873
rs146335642	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099366	GAGAACATAAAATTA[C/T]GTACCTGCTACAGAA	9873
rs146345787	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73005132	TGGAGCATTCTTATG[A/G]GCAAACATGCTATAA	9873
rs146349986	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73013700	ACAGTGTCTGCCACA[C/T]AGTAAATATTTTGTA	9873
rs146356678	snp	C/G	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:73104287	TTATTTATTTATGGA[C/G]ACAGAGTCTCACTCT	9873
rs146370009	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951387	AACATCTGGCATATG[A/C]TAACACAGCAAACGA	9873
rs146371430	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854432	CTCTGTCTGTCTACC[A/T]ATCTGTCTATCTGGT	9873
rs146404333	snp	A/G	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:72857542	CTCTTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	9873
rs146412375	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969433	TGTCTGAGAAAGAAA[C/G]AGAAAAACACTGAGA	9873
rs146431182	snp	A/T	0.030278	0.119257	intron-variant	FCHSD2	GRCh38.p7	11:73064301	AGTCTGTAGAGGGAA[A/T]TTTATAGCACTAAAT	9873
rs146447439	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911819	TCTCTTGAATTCAAG[C/T]GATTCTCCTGTCTCA	9873
rs146465744	snp	C/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72915610	GATCACCTGAGGTCA[C/G]GAGTTCAAAACCAGC	9873
rs146482717	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72846181	CTCCTCCTTTTGCTC[-/T]CTTTTTTTTTTTTTT	9873
rs146501539	snp	C/T	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:73134796	CAAAAAATAAGAAAA[C/T]AAATTATTCCCTGAT	9873
rs146519853	snp	C/T	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73047866	GAGCTAATGACTTTG[C/T]TATCTCATTTAAGCT	9873
rs146523967	snp	A/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73138382	AAATGGAGACAAAAC[A/G]CAATCAAGAAGTCTT	9873
rs146525743	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73124175	ACAGAAAACCAAACA[C/T]CGCATGTTCTCACTC	9873
rs146539536	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941271	CACATAGAATGACAG[G/T]AAATATTTGTTAAAT	9873
rs146555109	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73042070	TAGCTGGGATTACAG[A/G]TGCCCACCATCACAC	9873
rs146556084	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100267	CAAGAAAACCCTTCT[C/T]CTATTAACAACAACA	9873
rs146569969	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72946848	GCCTAGGGAAATTTT[C/T]CAAGCTTAAGTAAAC	9873
rs146573248	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886429	TTCTGTGTTACACCC[A/G/T]CAACAATCCCTCCCA	9873
rs146574639	snp	C/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73047520	GAACAAAAAATACTG[C/G]TCATTGACAGTACCT	9873
rs146588900	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72892322	GACAGGTAACTAATG[C/T]CACTGATTGGAAGAT	9873
rs146618245	snp	A/G	3.29669e-05	0.00405984	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72984177	AATCATTCCTTGCGT[A/G]GGTAGCTTTGGAATT	9873
rs146621880	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113875	GGTCTTGGTTAAGAT[A/C]CAGAAGAATTCTCTA	9873
rs146639431	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73116903	TTCCTCTTTATTCTT[C/T]GGTAAGAGTAATTAT	9873
rs146655632	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73073588	TATTTTTCTTTTAGG[A/G]TGGCTCACCTGTATG	9873
rs146656054	snp	C/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73019722	TCAGACATACTCTGG[C/G]GCTATTACAGTAAAG	9873
rs146674345	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73078099	GTACTCTTCTCTGTA[C/T]GTATATGTCAATTTT	9873
rs146675050	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72981294	CAATGCTGATCAAAT[A/G]TATGCATAAAGACTT	9873
rs146684346	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73079691	ATCAAAAAGAGAGGA[C/T]AGAAATATCTTTGTC	9873
rs146684896	in-del	-/TTTTATATTCCCCACTCTATTTTATAT			intron-variant	FCHSD2	GRCh38.p7	11:72941442	TAAATTATGTTGGAT[-/TTTTATATTCCCCACTCTATTTTATAT]GTCAGTTTGCTTAGT	9873
rs146685430	in-del	-/TATTTATA	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72903200	ATTTATTTATTTATT[-/TATTTATA]TATTTATTTATTTAT	9873
rs146690834	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72922800	TAAAATTCACCCAAT[A/G]TAAGTCACCATTTTA	9873
rs146691231	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72861892	GCTGAGATCATGCCA[C/T]TGCACTCCAGCCTGG	9873
rs146710424	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72865486	CAGAGGATATGTATG[C/T]CTCTAGAGGAGTGAT	9873
rs146714169	snp	A/G	0.030278	0.119257	intron-variant	FCHSD2	GRCh38.p7	11:72870849	AGCTTTCAGTGAGCC[A/G]AGATTGCGCCACTGC	9873
rs146742719	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093049	GCTGGAGGCTAAGGC[A/C]AGCCGCATGAGTAGT	9873
rs146749547	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72917592	TGTAGTTCCATATTA[A/G]TTCGAAGACTGGGCC	9873
rs146778682	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72994790	AACAAAAAAAAGATA[A/T]AGTGCAAACTGTATC	9873
rs146810894	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998846	AAGGCTGTAGAGAAA[C/T]TGGAGCCCTTGTGCA	9873
rs146822591	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72870922	AAAAAAAAAAAAAAA[A/G]AATTCCCCCTTTGAC	9873
rs146829948	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940761	GCCTGTTCATCATGG[G/T]GTTAATCAGCTAAAG	9873
rs146830265	snp	C/T	6.63196e-05	0.00575807	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843575	ATTAAAAAGGTTAGA[C/T]AAGGAGCAGATGTGA	9873
rs146834357	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850263	AGAGATGGGGTTTCA[C/G]CATGTTGGCCAGGCT	9873
rs146865639	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73113708	TTCCAGGCATTTGAA[A/G]AAACACCCATTTGTA	9873
rs146877390	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72948684	TTCTTTTTTTTTTTT[G/T]AGAGGCAGTCTCGCT	9873
rs146880819	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73071430	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	9873
rs146920683	in-del	-/AAAC			intron-variant	FCHSD2	GRCh38.p7	11:72880068	ACCAAAACAAGACAA[-/AAAC]AAAACAAACAAACAA	9873
rs146921791	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098718	CAAGATTTCTACATA[C/T]AAAAAATGAAAGTGG	9873
rs146951208	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73102492	AAGCAATGAAACGAA[A/C]CATCCATCAACTGAT	9873
rs146963849	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73125064	AAAGTGAGGGTGAAA[A/T]AAAGACATTTTCAGA	9873
rs146964933	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72950033	CCATCTCCTCACCAA[A/C]ACTTGTTATTTTCTG	9873
rs146967520	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048380	TAGGCATTTCAGAGA[A/T]AATTCCTGCAAAACA	9873
rs146973546	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73052683	GTGTGAATTGGACAA[C/T]TGGATTTATTCATCT	9873
rs146981432	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72894954	TCTAAAATCTGGAAA[A/G]TTCTGAATTTTGACA	9873
rs146981531	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953872	TCACATGTGAAAGTC[C/G]AGAGGTGACAATGTG	9873
rs146992571	in-del	-/TTTGT	0.0267878	0.112589	intron-variant	FCHSD2	GRCh38.p7	11:72892601	GTTTTTGTGTTTTTG[-/TTTGT]TTTGTTTTTTGTTTT	9873
rs147027575	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074361	GCAAGTATAAAATAT[A/G]TGCAAGCATATGTGC	9873
rs147056310	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73080717	CGGAGGCTGAGGTGG[A/G]CGGATGATCTGAGGT	9873
rs147068944	snp	C/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72925805	GCCAGTGGCTACAGA[C/G]CCCTGCCCCTTCTGA	9873
rs147072797	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028993	TCAGGTAGTTCTTCA[C/T]AGCAGTGTGAAAACG	9873
rs147075849	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73032604	AAAAAAAAGCACAAC[A/G]AAGAGGAAAAACTCA	9873
rs147085844	snp	G/T			missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867887	AAAGTGCCATTACTG[G/T]TCACTGCAGGAGGGC	9873
rs147088353	snp	G/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72873345	AAAAAAAAAAAAAAT[G/T]AATCTTTTCATGTGC	9873
rs147120594	in-del	-/ACAG	0.0279526	0.114869	intron-variant	FCHSD2	GRCh38.p7	11:73089278	GCTATAATAAAACAG[-/ACAG]TAACAAGTATTGGTA	9873
rs147129619	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890169	TCTTACACTGCTGAA[C/T]ACAAAAGCATCATCT	9873
rs147130311	in-del	-/AGATA	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:72846090	GATAGATAGATAGAT[-/AGATA]AGTAGTTACGATTAC	9873
rs147131855	snp	G/T	0.0314385	0.121371	intron-variant	FCHSD2	GRCh38.p7	11:72991678	ATGATTATCTCAATA[G/T]ATGTAGAAAAGGCCT	9873
rs147146693	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72895701	AAGCCTTTTGTGAAA[C/T]GCTGAAGAAATTAGG	9873
rs147161252	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997052	AGAAAGAGGGGTACT[A/G]CAGAAAAGCAAGTCC	9873
rs147216671	snp	C/G	0.0252325	0.109451	intron-variant	FCHSD2	GRCh38.p7	11:73063321	AACAACCGGTACCAG[C/G]CACTGCAAAAACATG	9873
rs147220007	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73067652	TAGGAGCTGAAAAGG[A/G]ACAAGTGCAAAATCA	9873
rs147233902	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72864334	GGGAGGCCAACGTGG[A/G]CGGACTGCTTGATCC	9873
rs147250096	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971021	TCACATTTGAGTTTC[C/T]CTAGCTGATGTGAGT	9873
rs147280772	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913983	AGGAAAAATCAATAT[C/T]ATAAAAATGGCCATA	9873
rs147320980	snp	C/G/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73040403	TGTGAGATGTATAAA[C/G/T]ACATACACACAGATA	9873
rs147325868	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73132861	CAGGTGATTCTTCCA[C/T]AGAATGGGAAAAAAA	9873
rs147327239	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73045831	CTAGATGATGAGTTA[C/G]TGGGTGCAGCCACCA	9873
rs147342795	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73039511	AACAGAGAGAGACTC[C/T]GTCTCCAAAAAAAAA	9873
rs147356248	snp	A/G	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72884465	AAATTTGGAAATAAT[A/G]TGATTAGAAATATAT	9873
rs147356363	snp	A/G	0.0314385	0.121371	intron-variant	FCHSD2	GRCh38.p7	11:72943078	CTCACTACAACCTCC[A/G]CCTCCCGGGTTCAAG	9873
rs147372030	snp	A/C	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73044631	ACAATAATAGAATTC[A/C]AACTCTGTCCTTAAG	9873
rs147418267	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73068813	CATCTCTACAAAAAG[A/T]AAAAAAAAAAAAAAA	9873
rs147426973	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73017575	AATTTGGTTTCACTA[C/T]TTCTAAGTATTGTGT	9873
rs147430682	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73110338	CTTGGCTTTGCTAGG[C/T]GATATTTTATTACGG	9873
rs147433238	in-del	-/AG	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:72896179	AGCATCTAGAATAAC[-/AG]GGAAAGATCATACAT	9873
rs147433955	snp	A/G	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73115385	AGATGGGGTTTCACT[A/G]TGTTAGCTAGGATAG	9873
rs147443220	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73022889	CAGAAATAGACCCAT[A/G]CAAATATAGTAAACT	9873
rs147444597	snp	C/G	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:72914129	AAGTGATTCTCCTGC[C/G]TCAGCCTCCCGAGCA	9873
rs147446351	in-del	-/CTT	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73100197	TCAGAATCCCACCTC[-/CTT]GTCACCAAAATGTAC	9873
rs147448318	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73017169	TTGTATTTTTAGTAG[A/G]CACAGTGTTTCGCCA	9873
rs147460968	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72918581	TCACAAAAAAGTACT[C/G]AATTTTGTCAAATCT	9873
rs147477108	in-del	-/C	0.0287284	0.116357	intron-variant	FCHSD2	GRCh38.p7	11:73130871	AGGTAATCTTTTTTT[-/C]CCCTCTCTTAAAGAA	9873
rs147533718	snp	C/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73090734	CTATTTGAATGTAAA[C/G]TATGTGCATATATAT	9873
rs147536321	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73094291	TATAGCAATGAGGAT[A/G]AAGGGCAATGGAACT	9873
rs147593241	snp	G/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73052904	CAGACTGGAGAGCAG[G/T]GGTGTGGTGTCAGCT	9873
rs147623099	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73058713	CAATTCTCCTGCCTC[A/G]GCCTCCCGAGTACCT	9873
rs147638036	snp	A/G	0.0275645	0.114116	intron-variant	FCHSD2	GRCh38.p7	11:72906004	TTCTAGATCCTTGAG[A/G]AGTTGCCACACTGCC	9873
rs147642368	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73014859	CAAATTCTTTTTTTT[C/T]TTGAGCTGGAGTCTC	9873
rs147653683	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72852277	CACTGCTGGTGGGAG[C/T]ATAAATTAGTTCAGC	9873
rs147665190	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72880868	CGAAAAAAAAAAAAA[-/A]GAAAACAACAACAAC	9873
rs147676031	snp	A/C	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72910069	GCACCTCTGCCCGGC[A/C]GCCCCATCTGGGAGG	9873
rs147695446	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73033005	TTAAGAGTACTTAGA[C/T]TGGCCGGGTGCGGTG	9873
rs147699293	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73123718	CTTCAAAACATCACA[A/G]AGGCTGGAGAGTATA	9873
rs147711868	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73036941	GTTCATCTGTTAACG[C/T]GGATCTGTAATTAGA	9873
rs147729004	snp	A/G	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:73127772	TTTAGGCACTTCACT[A/G]ATGCCTTCACCTGAG	9873
rs147740269	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72980918	CCAACAAATCAAATA[C/T]CCTGCTTTTAAGCTA	9873
rs147740939	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72880965	ATGCTTCTGGACATT[C/G]GTCAAGGGAGATTTT	9873
rs147756694	snp	G/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:72986443	CTCAATCTCCTGACC[G/T]TGTAATCCACCCGCC	9873
rs147757013	in-del	-/C	0.0283406	0.115616	intron-variant	FCHSD2	GRCh38.p7	11:73102183	TGAGATACCACTGAA[-/C]CACCCACTAGAATGA	9873
rs147759110	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880398	TGGTATTGTCACAAA[C/T]ACAGACACACAGACC	9873
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	9873
rs147800570	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73009312	GACCAGCCTGGCCAA[C/T]ATGGTGAAACTCCAT	9873
rs147801880	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73102004	TGCAGACCCAGATAA[A/G]ATCCAATGCTACAAT	9873
rs147816704	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73015497	TGTGTTTCATCATAG[A/G]TCACTCAGCAATTTG	9873
rs147819361	in-del	-/CTT	0.0520825	0.152737	intron-variant	FCHSD2	GRCh38.p7	11:72865601	ACAACGAGAACAGCC[-/CTT]CTTCTTTATCTCCTG	9873
rs147831158	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106370	GTGATGGCACCACTA[C/T]ACTCCACCCTGGGTG	9873
rs147844628	snp	A/G	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:72953733	TGAAGAAAAGATGCC[A/G]CCTTATGTTGTGTAG	9873
rs147845987	in-del	-/AAAT			intron-variant	FCHSD2	GRCh38.p7	11:72925544	AACAAACAAACAAAC[-/AAAT]AAATTTCTAAACACT	9873
rs147846068	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855783	GTGATATAGTGAATA[A/T]AAATAATATTTATAT	9873
rs147861164	snp	C/G	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72959726	GTTTACTGAAAGGAG[C/G]AATAGAAGTATTTAA	9873
rs147862583	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72860048	TCATCAGGTATTAGA[G/T]TCTCATAAGGAGGGT	9873
rs147866201	snp	A/G	0.0244538	0.107838	intron-variant	FCHSD2	GRCh38.p7	11:72855005	TAGGCCAGGCACGGT[A/G]GCTCACACCTGTAAT	9873
rs147891651	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73130038	GGCACCCGCCACCAC[A/G]CCCAGCTAATTTTTT	9873
rs147907021	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73133680	GGGCACCTATAATCC[A/C]AGCTACTCAGGAGGC	9873
rs147920406	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987460	CCTTAAATTCCTTGA[A/G]GGCACAAAGCTTACC	9873
rs147937273	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73086237	AACATGGCAAAACTC[C/T]GTCTCTACTAAAAAT	9873
rs147950266	snp	A/C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72930133	ACTAAATCAATTGAG[A/C/G]GGCCAGGAGGAAAAA	9873
rs147983751	in-del	-/AT			intron-variant	FCHSD2	GRCh38.p7	11:72931052	TCATGTGCCTCACAA[-/AT]ATATATATATATATA	9873
rs147997347	snp	A/C	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140468	CTTCTATTTCTAAAA[A/C]AGATTCAAAGACATT	9873
rs148012524	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72996560	ATGTAATAATTCTCA[C/T]AATCCTCATTATAAA	9873
rs148013752	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73093374	TGGTCTTGGGACCCA[C/T]AAAATTGCAAGTCGT	9873
rs148017817	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856088	GGACAGGCAGGATTG[C/G]CCTTCATAGGAGAGC	9873
rs148027442	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840358	AAATTGCAAAGTATC[C/T]GACTGGATTACCGTG	9873
rs148042453	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937527	ATGGACATATGGGAC[A/C]ATTAATGGAAAGGCA	9873
rs148095650	snp	A/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72982897	CAAGCACAATGGCTC[A/G]CACCTGTAATCCCAG	9873
rs148097422	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73115210	CTTCGACAGAACAGC[A/G]CTGAGTTCAATGGAG	9873
rs148100572	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73061438	TACCCCAGTGGCACC[A/G]GGAATACCAGTGAGA	9873
rs148115745	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73113579	TCGCCATGTTGCCAA[A/G]ACTTGGCCTTGATGC	9873
rs148154083	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73054879	GAGGCAGAGGTGGGA[A/G]GACTGCTTGAGACCA	9873
rs148161779	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72917314	GCATGTGGCTATCCA[A/G]CTGTCCCAAAACCTT	9873
rs148167254	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72903618	TTTACATACCTTGGG[A/C]AAGAGTGGAAATCGG	9873
rs148171052	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73003055	ACAATAAAAAGACAA[A/C]TCCTTTCATTAAAAA	9873
rs148177966	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72862594	AAGTCCTAAATAAAT[A/G]GAGAAGTATATTATG	9873
rs148197824	in-del	-/AAAG	0.0437281	0.141251	intron-variant	FCHSD2	GRCh38.p7	11:73125787	AAAAAGAAAAAGAAA[-/AAAG]AAAGAAAGAAAATGG	9873
rs148222210	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72906857	TGAAGTCAGGTAGCA[C/T]GATGTCTCCAGCTTT	9873
rs148237286	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72888973	TCTTTTTTCTTTTTA[C/T]TGAGACAGAGTCTCG	9873
rs148240882	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73135526	ACAATCCTAAGAAGA[A/G]AAGTACACAGACTCT	9873
rs148277938	snp	A/G	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73130166	GGTGTGAGCCACCGC[A/G]CCTGGCCCATAATCT	9873
rs148305589	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73033997	ATCATGAAAATATAA[C/T]AGACAATTTTAATAC	9873
rs148313080	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73017046	GGAGTGCAGTGGCGC[A/G]ATCATGGCTCAATGC	9873
rs148344441	snp	A/G	1.64787e-05	0.00287038	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72849782	AACAACTTTGCAGGT[A/G]AGTGGATAATTTCTT	9873
rs148345193	in-del	-/CCC			intron-variant	FCHSD2	GRCh38.p7	11:72913822	AAAAACCAAAAAAAA[-/CCC]AAAAAAAAAACAAAA	9873
rs148366306	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73104053	ACAGCTCCCAAGTAC[C/T]TGAATGTCAGCCATC	9873
rs148370809	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72867449	ACTAAGCCCACGTAC[G/T]AAGAAGAACATTCCT	9873
rs148377994	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72951000	CTTCTCCATGCTCTC[C/T]TTCCCCTATCCACTG	9873
rs148383061	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73048642	TAAGTGCCGGAAGTA[C/T]GAAAAAGCTGGAAAT	9873
rs148393710	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72848611	CATCCCCCCAGTGTA[G/T]CACATATTGGGCACT	9873
rs148398905	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132229	ACGATAACTTCCTTT[G/T]GTACCTTGAATAAGA	9873
rs148410888	snp	C/T	8.47997e-05	0.00651096	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72985067	GAAAACTTACCTTTA[C/T]ACTTGCCTTCTGTAA	9873
rs148416020	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085042	AAATCATTTAAATTC[A/C]CCAAATGACTTGATT	9873
rs148444805	snp	C/T	8.23934e-05	0.00641794	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72887547	GTTCTGATACAGCAG[C/T]TCCATGACACTCCAG	9873
rs148461912	in-del	-/TTC	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:73110145	TACTGGTCTGTAGTT[-/TTC]TTCTTTTTTTTTTTG	9873
rs148468971	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73023031	TTGACACATACCTCA[C/G]GAGTTACACAAAAAT	9873
rs148479323	snp	C/T	0.0221141	0.102801	intron-variant	FCHSD2	GRCh38.p7	11:72921185	ATTTAATTTATCAGA[C/T]AAAAAACATTTGCCA	9873
rs148482066	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864517	CACCACTGCACTCCA[A/G]CCTGGGCGATAGAGG	9873
rs148501569	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73050915	AACAAAGGTCCTCCA[A/G]CTGTTTGTTACTGAT	9873
rs148512536	in-del	-/TTTTG	0.499801	0.00998203	intron-variant	FCHSD2	GRCh38.p7	11:72866257	CAACTCTGTTCTGTT[-/TTTTG]TTTTGTTTTGTTTTT	9873
rs148531899	snp	A/G	0.0205511	0.0992634	intron-variant	FCHSD2	GRCh38.p7	11:72964462	TTCCTTCCCCTTTGT[A/G]CTACTACCACACTGT	9873
rs148535285	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72908942	TACAGGTGTGAGCCA[C/T]TGCATGTTGCCCTGT	9873
rs148554472	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73047098	GTGAATATAATTCTA[C/T]TTTTTTATAAAGGAA	9873
rs148555291	snp	C/G/T	0.00319074	0.0398324	intron-variant	FCHSD2	GRCh38.p7	11:73137840	TGCATGGGCATGAAA[C/G/T]GGTAGTAACTAAGCC	9873
rs148569492	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891922	ATGTTAAAGACCCAA[C/T]TGAAAATTACTTGAA	9873
rs148570856	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72993961	AGGCTTTGGGCTTCT[A/G]TGAGTACGGTGTATC	9873
rs148622322	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73036107	CTAAAGGCTAAGAGT[A/T]GACTGGCTTGGACAG	9873
rs148631389	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73111305	GCTCCAGTATTGGGT[A/G]CATATATATTTACAA	9873
rs148634930	snp	A/C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72879948	AGCTTGACGTGAGCC[A/C/G]AGATCGCGCCATCGC	9873
rs148649236	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73124270	TATTGTGGGATGGGG[G/T]GACGGGGAAGGGATA	9873
rs148677276	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119662	CTGTGTTGCCCAGGT[G/T]GGTCTCACTCCTGGC	9873
rs148679298	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72971563	TTGGTAATGGAGAAT[C/T]ATGTACAAAGGACCT	9873
rs148681476	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73105938	TACCTATAGAAGATA[C/T]CTGGCAGAAGCAAGG	9873
rs148694719	snp	A/C	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72953339	CCTTTTTCACAATTT[A/C]TTTTTCAAAAAATCT	9873
rs148700453	in-del	-/A	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72983483	TAAAAAATTAAAATT[-/A]AAAAAAGCTTCATAA	9873
rs148712178	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73007045	TAAGTCCTTTGTACA[C/T]ATCATCTACTATTTT	9873
rs148713592	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100784	CTATTGGGTAGCTGA[C/G]TCTAAATCTGGTGCT	9873
rs148717235	in-del	-/ATG	0.498813	0.0243321	intron-variant	FCHSD2	GRCh38.p7	11:72958993	ACTCATCAGTAAGAT[-/ATG]TGTGTGTGTGTGTGT	9873
rs148746554	snp	A/G	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:72857931	TTGACTATGTCACTT[A/G]CTTGTTGTGTGACCT	9873
rs148766705	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096014	TATCCTAAAGTGCTA[C/T]AGAAAAAAACAAAAA	9873
rs148778084	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940246	CTAAATGGGGCTTTG[C/T]GTGTTTATATTATGC	9873
rs148783664	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73040965	CCCACATATCAGTGA[A/G]TGAGAACATGTGATA	9873
rs148794915	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72885494	ATAATAGGTCATCTG[A/G]CCTAAATGAAGACTC	9873
rs148853768	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72911537	AATGGCACTGGTATT[C/T]TGAAAGAGACTGCAT	9873
rs148870698	snp	C/T	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:73015579	TATATAAAATATAAT[C/T]TTGGCTTATATAAGA	9873
rs148876541	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139209	AGTTAATATTTTTCA[C/T]GAAACCAACACGAAG	9873
rs148884154	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72855868	TAGAGGAAATGACTG[A/C]CTTGCTTTTTATATA	9873
rs148888549	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72995428	AAAACTGGGCCAGGT[A/G]CGGTGGCTCACACCT	9873
rs148930931	snp	C/T	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:73130064	TTTTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	9873
rs148936091	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72899675	CCAGGAGGTTGAGGC[A/G]CAGTGAGCCGTGATT	9873
rs148947133	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981996	CAAAAACTATATATA[C/T]TAAAACACCTAAACC	9873
rs148968336	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902631	TGAAGATTGTAGTCC[C/T]GGACCACCTAAAGAG	9873
rs148983701	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122626	TTAATGAGGGAAAAA[C/G]AAGGGGACAGTTTAT	9873
rs149000225	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072076	TGAGTGAAGACATAC[A/G]CAGACCACTATGTCC	9873
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	9873
rs149032628	snp	C/T	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:73103619	CTTTATGCCAACACA[C/T]AGTTCAATTAAACTA	9873
rs149048029	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019462	TATCTATTTTTTTAA[A/G]TTATGAAATTAATTT	9873
rs149064144	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72960127	CACAGTGCCAGGATC[G/T]ATTTCTGGTGAGGCT	9873
rs149064589	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72860366	TGTAACAGTTACCAA[C/G]ATATACGTTTATACT	9873
rs149082689	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098367	TTTCTGTCCCCTTCT[A/G]TTAATTGATTTCTAG	9873
rs149086193	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73043915	AACCTCAAGATTAAA[A/G]GAGCCTGGATCATTG	9873
rs149095791	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941924	CATTAAAAAAGTTTA[C/T]AAAAGCATAAAAAAG	9873
rs149135783	snp	G/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73134174	AGTCTCTGAGACACT[G/T]AAAAAAAGTCTCAGC	9873
rs149138489	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73087293	TTTATACAGTTGTAC[A/G]ATATGTGTTTTAAGC	9873
rs149148129	snp	A/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72851519	GCCGAGGTGGGCGGA[A/T]CACAAGGACAGGAGA	9873
rs149150087	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72947103	GTCACTCTGGTTTAA[C/G]AGCTGCATGCCCCAT	9873
rs149150936	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988212	AGTCAGCACACTGAC[C/T]CTGAGTCTCAGCTCT	9873
rs149152120	snp	C/T	0.0174175	0.0916809	intron-variant	FCHSD2	GRCh38.p7	11:72931086	CCTACTATATACCCA[C/T]AATAATTAAATTTTT	9873
rs149192643	snp	A/G	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:73079689	CAATCAAAAAGAGAG[A/G]ATAGAAATATCTTTG	9873
rs149208066	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72924268	ATTTTGATGCAGTCT[A/C]ATTTAGCTATTTTTC	9873
rs149209481	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027694	GGCATTTCAGAGATG[G/T]TCGCTGCACTCCCCG	9873
rs149242627	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73053908	TAACTTGTTGTCTGT[A/G]ATCTAAAAATTTTAA	9873
rs149251166	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73131662	TAAGCCAAGATCGCA[C/T]CACTGCACTCCGGTC	9873
rs149262603	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72983999	CTGGCTACTCTTTTA[C/T]AGATTCAATCCCATA	9873
rs149301323	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73124870	ATACTAGTCACATTA[C/T]ACTCAAACTGTAGGA	9873
rs149310362	snp	G/T	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:72894875	AAAATACTATGTTTG[G/T]TCACAGGTGCTTCCC	9873
rs149313870	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839789	GAAGAGATCGGATTG[G/T]CAGTTATAAATCTGA	9873
rs149314558	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72978664	GTGACTGAGTTCTCA[C/T]GATATCTGATGGTTT	9873
rs149331331	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73075758	GGGCAGAGTTTGCAG[C/T]GAGCCAAGATCATAC	9873
rs149345507	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72971183	GAACAGGTCAAAATA[C/T]AAAAATCAATCATAT	9873
rs149346859	snp	A/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72869967	AAATATCTTTCACAG[A/T]TTGGCTGAGTTATTT	9873
rs149408946	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73046375	ATGAATGGCCAATAC[A/T]GCAAGAATGCATTGT	9873
rs149453288	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:73010308	CTGAATTGTTTTTCT[A/G]ATTTCTCTGTACTGT	9873
rs149462015	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73090194	AAATGTTTACAAATA[C/T]ATATTTATGGTAATT	9873
rs149469294	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853445	TTGGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG	9873
rs149474328	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933398	TGAAGATGGGAATGG[C/T]GGGCAGAGGACAGGG	9873
rs149491382	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73035234	GTCTCGCTCTGTCAC[C/G]CAGGTTGGAGCGCAG	9873
rs149523444	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72887947	TAAGTGGAACACTGA[A/C]TTTGAGACACCTGTG	9873
rs149528333	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030135	AGTTATAAAACTGCT[A/G]CATGATAGCAGTACC	9873
rs149556223	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920831	ATAGGAAAACAGATA[C/T]ATGACAGGACTTCAA	9873
rs149596681	snp	C/T	0.0441095	0.141807	intron-variant	FCHSD2	GRCh38.p7	11:73066036	AACCAAAAAAGAGCC[C/T]GCATTGCCAAAACAA	9873
rs149602034	snp	A/G	0.021333	0.101051	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73142938	GGGCGCAGCATGCCT[A/G]TGGGATACGAGAATT	9873
rs149611292	snp	G/T	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:72913614	TTTATTGGCATATAT[G/T]GTTCACAGTAGCCTC	9873
rs149612773	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73016926	GTTAAGAATTGATTT[C/T]AAACTGCTCATTCCA	9873
rs149618147	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73095814	CAAACAAGCCACGCT[A/G]GCAGAAACTGAGTTG	9873
rs149626850	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72857827	ATCTTCTTGTACTCA[C/T]TAAAAACACCTCTGA	9873
rs149664177	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72973622	GGAGATGTTTTGGGA[A/G]GGGTCACCTGGGAGA	9873
rs149685109	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72884312	TTGAATCTAGATGTT[A/G]GGAAATACATGTTTA	9873
rs149704195	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73115992	ATCACAGGGGCACAA[A/C]TGTGTTATCCACGAG	9873
rs149707276	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73063694	GAAAGAGACAAAGAA[C/T]GGTATTACATATTGG	9873
rs149708497	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73101974	AGTCCAAAATCTGCA[A/G]GGTAGGCCAGAAGCT	9873
rs149758898	snp	A/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73104929	TTACAATATAGTTTT[A/T]CACGTTTAAATGAAT	9873
rs149771427	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014509	TCAAGACACCTTCCA[C/T]GATATCAGTAGGCCA	9873
rs149772506	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72952323	GTGTTCACCAAGTTT[A/G]ACTATCTTTTTTTTT	9873
rs149806975	snp	C/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:73037463	ATCCTCAACTTCTGG[C/T]AACTACTGATCTTTT	9873
rs149828222	snp	C/T	0.281841	0.247964	intron-variant	FCHSD2	GRCh38.p7	11:72944315	ATATGATTATCTCAA[C/T]AGATGCAGAAAAGGC	9873
rs149843295	snp	G/T	0.000153988	0.00877327	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902587	AGGGCTGGGGTTTGT[G/T]AAATACAGCGTTTTC	9873
rs149845018	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72890668	TGGAAAGTGCTTCAT[A/G]TAACTTTTTTTTTTT	9873
rs149856886	in-del	-/TTGTTGTTG			intron-variant	FCHSD2	GRCh38.p7	11:72961406	TTTTTAAGAAGTTTT[-/TTGTTGTTG]TTGTTGTTGTTGTTG	9873
rs149860774	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73031657	GACCAACAAAGGACC[A/C]TATTAACCAACACTG	9873
rs149862249	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73121133	AAAAGCAATTAAGCA[C/T]ACCCTTTGGGGTCTC	9873
rs149878215	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72924084	TTTCACTTTCTTGAA[A/G]GTTTCTTTTGATGTA	9873
rs149924832	snp	C/T	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72879500	ACAAGAACTTTAAAA[C/T]TGCTGTTATAAATAT	9873
rs149929919	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019027	GCAACATATGGGTTA[C/T]TGCCAAACAAGTGGC	9873
rs149932797	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72860148	GCTGGTCTGACAGGA[C/T]GCAGAGCTCAAGCAG	9873
rs149982029	snp	A/G	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:73057032	AGCTTGCAGTGAGCC[A/G]AGATCACACCACTGC	9873
rs149985061	snp	G/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73005678	ATAAGGTCTTGCTCT[G/T]CCACTCAGGTGGTAG	9873
rs149989276	snp	C/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73041776	TCAATTTTGTGTTTT[C/G]GTTTGTTCACAGTTT	9873
rs149992039	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73059279	TTTACCCTCCGTGGG[-/T]TTTTTTTTTTAACCC	9873
rs149998754	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73077130	AAAAAGAAAAAAAAG[-/A]AAAAAAAAAGTTTGT	9873
rs150002719	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72851080	GCACTACAGCTGGGG[C/T]GACACAGCGTGACTC	9873
rs150003161	snp	C/T	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:73134064	AGTCACATCATGTAA[C/T]TTACATGATATGTAC	9873
rs150038311	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72998065	TGTTAAATATTCAGA[C/T]TGAAGTACACAGAGA	9873
rs150052638	snp	C/T	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72940046	GTGTTACAGCCTGTA[C/T]AGAAAATGCAAGCAA	9873
rs150056236	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73127681	CAAGAGTAAATTGCC[A/T]ATCATCAATTATTAA	9873
rs150073025	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73078916	ATAGAGATGGGGCCT[C/T]ATTATGTTGTCAGGC	9873
rs150078842	snp	C/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73107249	TAGTAGAGACAGGGT[C/T]TCACCATGTTGGCCA	9873
rs150087439	in-del	-/AAAC	0.244643	0.249943	intron-variant	FCHSD2	GRCh38.p7	11:72868691	GCAAGACTCTGTTAA[-/AAAC]AAACAAACAAACAAA	9873
rs150094087	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72954362	CACAGGTGCATGCCA[C/T]CATGCCTGGCTAATT	9873
rs150145659	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73048138	ACTTGACAATGTTAG[C/T]ATATCAAACTGCAAA	9873
rs150148356	in-del	-/CCCCC			intron-variant	FCHSD2	GRCh38.p7	11:73123137	TTTATAAACAAGCCA[-/CCCCC]AACCGCCACTCTCTT	9873
rs150168360	snp	C/G	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73124640	GTGTGCCTCTAATCC[C/G]AGCTACTCAGGAGGC	9873
rs150169582	in-del	-/T	0.031825	0.122064	intron-variant	FCHSD2	GRCh38.p7	11:72971372	TATAATCCCCTTTCC[-/T]TTTGAGTGTCAGTAG	9873
rs150180023	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034490	ACTAATGTTAAAATT[C/T]GGTACCAGAGGCTGA	9873
rs150181977	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73029773	TTGAAAATTAGGACA[C/T]TGAAGGGCAATTGCA	9873
rs150228321	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935476	TAAATATCAAGATGA[C/T]GATAAATGTGAGTTG	9873
rs150235624	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114012	GGGCCTCTGTCCTTC[C/G]CTTTAGGGTGGCAAT	9873
rs150246305	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72863062	TGAGTAGCTAGGACC[A/G]CAGGAATGTACCACA	9873
rs150249064	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72962501	TGATATTCACTGTAA[A/G]AAGAACAGGAGTTTA	9873
rs150286279	snp	A/G	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73059903	ATTTGTTGTACCAAA[A/G]CTTTGCTTATATCTG	9873
rs150302160	snp	C/T	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72907036	CCATTTGTTTGCGTC[C/T]TCTTTTATTTCGTTG	9873
rs150321791	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73136386	GTAACATGGTAAGAC[A/C]CCATGTCTACAAAAA	9873
rs150332516	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72853209	ATACATGATTAAATG[A/G]TTTTCAACAAGGATG	9873
rs150363993	snp	A/G	0.000219452	0.0104727	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73015858	GCCAATCTCTCTTCA[A/G]GTATTGACTAGCCAA	9873
rs150368027	snp	C/T	0.0232847	0.105357	intron-variant	FCHSD2	GRCh38.p7	11:72846203	TTTTTTTTTTTGAGA[C/T]GGAGTCTCACAGTGT	9873
rs150370971	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73097925	GCGATCCTCCTGCCT[C/T]GGCCTCCAACTGGCT	9873
rs150383005	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72941821	AATCTTTGTTTTTGA[C/T]CAGGGAATGTAGCTT	9873
rs150417770	snp	A/G	2.01177e-05	0.0031715	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867872	AATCGTACCGAGTGT[A/G]AAGTGCCATTACTGG	9873
rs150420652	snp	C/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:72886384	ACTAATCAAATACTA[C/T]TCATCTGCCAGCATT	9873
rs150430378	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73118244	AAATTGCTTGGACTC[A/G]GCAGGCAGAGACTGC	9873
rs150436386	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987958	TACAATAAAACAAAT[C/T]AGAGAAATATTAAAT	9873
rs150445293	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72970613	CCACTGGTTTCTTCT[C/G]TGCATTACTTTCACT	9873
rs150447374	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73065626	TCGTCTCAGTCCAAA[A/G]TCTCCTTAAGCTGAT	9873
rs150462084	snp	C/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:72913257	TAGGTTGCATGCATC[C/T]AGGAATTTATCCATT	9873
rs150536129	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73066614	AGGGCTAATATCCAG[A/G]ATCTACAAAGAACTT	9873
rs150552509	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025527	AGATAATGAGAAAAA[A/G]ATAACTAATGGGTAC	9873
rs150604096	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927172	AAGATCCTTCAGATA[C/T]GAGCTGCCTTCCATT	9873
rs150608202	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73062756	AAAGAATAAAAAGGA[C/T]GAACAAAGCTTCCAA	9873
rs150620198	snp	G/T	0.0337553	0.125452	intron-variant	FCHSD2	GRCh38.p7	11:72869157	GGTGATCCACCTGCT[G/T]CAGCCTCCCAAAGTG	9873
rs150637500	snp	C/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73014217	GCTCACTGCAGCCTT[C/G]AACTCCTGGGCTCAA	9873
rs150690788	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098980	ACACTTTGGGAGACT[A/G]AAGCAGGAGGATCAC	9873
rs150699430	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72849205	AAGAGAAGATTCATG[C/T]ATTCACGCCTCCCTT	9873
rs150705258	snp	A/T	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72944085	ACCAAAGCCTGGCAG[A/T]GACACAACAAAAAAA	9873
rs150747224	snp	A/C	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73119845	TACCATAAATATACA[A/C]GGATGTAAATAAGAA	9873
rs150761733	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933075	ATAAAATATATATAA[A/C]CTTGCATGCCTTCTT	9873
rs150763783	snp	A/C	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:72972307	TTACCTCAAAAAACT[A/C]TAAAATTAAGATCAT	9873
rs150763977	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73068952	TAAAGAAGGTCGAGG[C/T]TGCAGTGAGTCATGA	9873
rs150767189	snp	C/T	0.000206872	0.0101683	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841499	GGGAGCTCCTCTTAT[C/T]TGGGCTGGGGTAGGG	9873
rs150817025	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73109402	CTTCAATTTCTTTCA[C/T]CAATGTTTTATAGTT	9873
rs150822952	snp	C/T	0.0158469	0.0875917	intron-variant	FCHSD2	GRCh38.p7	11:72875566	ACTCCTGGCCTCAAA[C/T]GATCCTTCCGCCCTC	9873
rs150846197	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73055850	CAGAAAGTAGATTCA[A/G]GGGCTGTGGGAGGAG	9873
rs150863314	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905088	GTTCATGTCCTAATT[C/T]CCAAAACCTGTGAAT	9873
rs150900658	snp	A/C	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73049319	CTCATACCCACAACA[A/C]TATTAAATTTGGTTC	9873
rs150901635	snp	A/G	0.00358779	0.0422022	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142057	CGGACCCCAGCCAGA[A/G]AGCGAGTGTGAGGAG	9873
rs150912808	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72896813	ATATGCTTGCCTTGT[A/G]GATTTTTGTTTTGTT	9873
rs150917575	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997515	AAATCAAGAAAAACC[G/T]CAGGCGGTTAAAAGA	9873
rs150935795	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72871881	ACAGGTGTGAACTGC[G/T]GTGCCCAACAGGTAC	9873
rs150945500	snp	C/T	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73107046	AAAGCTATATATATA[C/T]ATATATTTTTAAATG	9873
rs150954696	snp	A/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73015748	TGTTACATTATCTAT[A/G]TGTAACATAGCTTTA	9873
rs150967585	in-del	-/C	0.0410537	0.137264	intron-variant	FCHSD2	GRCh38.p7	11:72916466	AACAGGTATGCAGCA[-/C]CATGTCTGGCTAATT	9873
rs150989206	in-del	-/AAAT			intron-variant	FCHSD2	GRCh38.p7	11:72864608	TGTTTGTCAATTAAA[-/AAAT]AAATAAATAAGAGTA	9873
rs151008705	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101211	ATAAAAAGGCCACAT[A/G]AAATAGCAGATAAAT	9873
rs151062289	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73138127	CAGGAGCAACAGACT[A/G]TATCAACTTAGCTTA	9873
rs151064107	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994303	CTTCTAAAAAGACCC[C/T]TTGTGGGCACTGCAC	9873
rs151065029	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73091277	GGCATGGTGGCTCAC[A/G]CCTGTAATCTCAGCA	9873
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	9873
rs151082202	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934972	CACGTCCTTTCCAGG[C/T]AGCTATTAGGCCACA	9873
rs151099675	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73073164	TTTTACCAACACCTC[A/C]GTGGTTAGCTAATTG	9873
rs151135971	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72980015	CAGGAGGGGATGAGA[A/T]ATAATCCAAAGCTGA	9873
rs151152781	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73112776	GCCTCAGCCTCCTGA[A/G]TAGCTGGGGTTACAG	9873
rs151167846	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72960751	TGTGGAGAAAGGGTA[C/T]GGGGCAAGGGACAGG	9873
rs151168876	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73059610	ATGGTAAGAGGAAAA[A/G]CAAAATTAGTCTATG	9873
rs151217357	snp	C/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:72914691	GCCATATGCAGAAAA[C/T]TGAAACTGGACCCCT	9873
rs151232993	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72901105	TTTAAACAATTGCCA[A/G]TTGGGGCCGGACATC	9873
rs151239951	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72893473	GCATATGCCATCACA[C/T]GCAGATAATTTTTTT	9873
rs151277201	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73041249	GATAAATATCCAGTA[A/G]TGAGATTGCTGGATC	9873
rs151288942	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72885763	CCAGTGTTTCTTAGA[G/T]TAGATGAGGGCTTGC	9873
rs151307612	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73028531	ACTTCCTTGTCTCAG[A/G]TGAGACTTTGGCCTT	9873
rs151308853	snp	C/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73117697	AATTTTTCAATCACA[C/T]TGTAAAGAATTTTAC	9873
rs151320549	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73049873	GCACAAAAGGACCAT[-/A]AAAAAAAAATTGTTT	9873
rs180682661	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72850326	CACTTCGGCTTCCCA[A/G]AGTGCTGGTATTACA	9873
rs180775596	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72974183	TGGTTCATGGTTCTC[A/G]GGACTGGGAAGTCCA	9873
rs180797947	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932434	TACAGACCACATTAT[C/T]TGAACTTGGCATACC	9873
rs180798153	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73031411	AGGGCGGGAGGTGGA[A/G]GCTGCATTGAGTTGT	9873
rs180803981	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73012926	TTCCCTACAACTTGA[C/T]TTCTGCTACAATTTC	9873
rs180805587	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952300	TCCATACACTTTTTT[A/G]TTTGCTTGTGTTCAC	9873
rs180805990	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72995109	TCTCACTTCTTTCAC[C/T]TATCAAAACATTTTT	9873
rs180816339	snp	A/T	0.0501905	0.150254	intron-variant	FCHSD2	GRCh38.p7	11:72878000	ACTGTCTCAAAAAAA[A/T]TTTTTTTAAATATAT	9873
rs180826664	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869325	ACAACAATCTTGATA[A/T]TCACTAGCAATTCTT	9873
rs180829310	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72914512	AGGGCCACAGCAACC[A/C]AACAGCATGGTACTA	9873
rs180829720	snp	A/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72885285	AAATGCTACAGATAT[A/T]CAAAACTGAGAAAAC	9873
rs180837744	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840817	CGGGGAAACATTAAT[C/T]CCTTACTTTCAATTT	9873
rs180859719	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73139801	ACTAGTAAGACTTTT[A/T]AGGTCCTTGTTTTTT	9873
rs180859870	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121885	CATTTTTAACAAGTT[C/T]CAGATGGTGTTGATA	9873
rs180862222	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895748	CTTAACTGTCAGTAT[G/T]GCTAATTCTAAAACG	9873
rs180881361	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836799	TAAATACAAACTTTT[C/T]ACAGCCACTGTAAAG	9873
rs180887054	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72860810	GTGACAGAGCAAGAC[C/T]CTGTTTGAAAAAAAA	9873
rs180914478	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73023608	AATAGTATGGCCACT[C/T]TGAAAGACAGTTTTG	9873
rs180916909	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73079618	CTATAGAAAGAATAT[A/G]CTAATTATTTCAGAG	9873
rs180923953	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099454	ACCCCAAGGTATATA[A/C]TCGAGAGAAAACAAA	9873
rs180937592	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73051915	CACACACACACACAC[A/C]CCCCACACACACTGA	9873
rs180947828	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131158	AGCTTGAGGCAGGCA[A/G]ATCACTTGAGACCAG	9873
rs180955809	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73086198	TGGATCACTTGAGGC[C/T]AGGAGTTTAAGACAG	9873
rs180956528	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067839	TGAGGTACCTGCATT[A/C]GTCCATTTTCACACT	9873
rs180959279	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73041480	ATTTCCCTGATGATT[A/G]GTGATGCTGAGCATT	9873
rs180968003	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73060075	AGGATACACTGCTAT[C/G]AGAGATGACTAACAC	9873
rs180977770	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73006019	CTCAAGTGGTCCTCC[C/T]GCCTCAGCCTCCCAA	9873
rs180978966	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875265	AAAAAAGCTCCAAAC[A/G]GCTTTTATCATAGGT	9873
rs180982227	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72854773	AAAGCAGAATGGTGA[C/T]TGTCAGAGGCTGCAT	9873
rs180984692	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72903136	TTCTTGAGGAGGTTA[C/T]ACTCTAATTACCATC	9873
rs180987795	snp	C/G	3.34286e-05	0.00408818	intron-variant	FCHSD2	GRCh38.p7	11:72849719	ATCTTCAGAGTTAAT[C/G]AGAATTTAATAACAT	9873
rs180997092	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73108762	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCTTGTT	9873
rs181009649	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881046	AGGACTACATTAAAT[C/T]AAAAACTCTATGCAG	9873
rs181018773	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72990108	ATGGACAGATAAAAG[A/C]AAAATAACCACTCAT	9873
rs181019062	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864993	TTACATTCTGTACTA[C/T]AGCATGATACAGAAG	9873
rs181021437	snp	A/G/T			intron-variant	FCHSD2	GRCh38.p7	11:72926936	AGTGAAAAAAATGGC[A/G/T]ACTTGGTGCACTAGT	9873
rs181030563	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72962602	GAACTAAATTCCCCC[C/T]TTTTTTTTTAAACTA	9873
rs181035671	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72845862	CTTTGAACCTCAGTT[G/T]TCTTTTTTCGTACTA	9873
rs181064660	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72864132	AGAGTAGACTGGCAG[G/T]TTGCCCTTGCACATT	9873
rs181082910	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73013508	ACCGCTGACATGTAG[C/T]AGGTATTTCATATGT	9873
rs181083352	snp	A/T	0.0170251	0.090679	intron-variant	FCHSD2	GRCh38.p7	11:73006085	GCTATTTTTTTTTTT[A/T]AATAAAAATAGTATC	9873
rs181089609	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72907409	GCATCCTTATCTTGT[A/G]CTGGTTTTCAAAGGG	9873
rs181090307	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004674	CTACCTTGGTTAAAT[A/C]TAAAACTGTTTACAT	9873
rs181091131	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040804	ATCCGACTGTGCTAT[A/T]AAATACTAAAACGTA	9873
rs181092521	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921616	AAGCTACCTTGTATC[A/G]GCACCTCTCTTTTTG	9873
rs181092522	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72985290	TTTATTTTACTACAG[C/G]AAGAATTTATTATCA	9873
rs181097056	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058752	TTTGAATTTTTAGTC[A/G]AGATGGGGTTTTACC	9873
rs181097667	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941213	TCCTTCAAGGGACCA[A/G]AGGCCACATGAGTCT	9873
rs181099149	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72964166	GAAATGATGTAACAG[A/C]AATCAAGAGAATTAC	9873
rs181104804	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72996009	AAAAAATAATAAACA[C/T]AAAGGTTATGTAGAA	9873
rs181110602	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73022554	GGATCTGTATGTGGA[A/G]AAGTCCATAATACTA	9873
rs181111662	snp	A/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73052415	GTATAATTTTTTTTT[A/T]AAAAAAAGACACCTG	9873
rs181112298	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73098611	TAGTCCAGGAAAAAA[A/C]AAACAAACATCTATG	9873
rs181112902	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974698	ACAAGTACCAGTGGT[A/G]AAGGCACAAATATGA	9873
rs181116107	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73068626	TAACAAAATTAACAA[C/T]TGGAACACACATTTG	9873
rs181125043	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73031997	CAAGAGGAACTATTA[A/T]CTAAATTATGGTCAT	9873
rs181128661	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73120685	AGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG	9873
rs181136214	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73077726	ACAACATAAACTACA[A/G]AATAGTTAATGCTAA	9873
rs181141546	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72914836	TGGGCAAAGATTTCA[C/T]GATGAAGATGCCAAA	9873
rs181152218	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72933337	TGTAGTAGGAAAGAA[C/T]TAAACCAACTCACAG	9873
rs181178523	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896226	AGCTTTTTGCTGTCA[C/T]GATCTGTGAAGATCT	9873
rs181185749	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73085827	AGAGCAGAGTTACCA[C/T]ATTATTACATTCAAA	9873
rs181214814	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110111	TGTGGAGGATTTTTG[C/T]ATCAGTATTCATCAG	9873
rs181228674	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881688	ACACACAATGGAATA[C/T]TATTCAGTCATAAAA	9873
rs181230154	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72865618	TCTTCTTTATCTCCT[A/G]TTAAAATTCTTCAAA	9873
rs181248924	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086454	CAATCTCAAATCAAC[A/T]GCCTAACTTTACAAC	9873
rs181251366	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846616	TTACCCCAACTAAAG[A/G]CAGTGAGCAGTAAAT	9873
rs181263952	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73138421	ACAACCAACAGAAAT[C/T]ATTACAACTACTGAC	9873
rs181265370	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72903629	TGGGAAAGAGTGGAA[A/G]TCGGCATCTGATGGG	9873
rs181282423	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72917087	CCTTTCGGGTTCAAG[C/T]GATTCTCCTGCCTCA	9873
rs181296282	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956579	AGATCAAGGCGCCAG[A/C]AGATTTGGTGTCTGG	9873
rs181359503	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115896	AACATCCACAAAATG[A/C]CTTCATGGCAACATG	9873
rs181363447	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73064838	TGAATAAACCAATAA[C/G]AAGTTCTGAAATTGA	9873
rs181367368	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73046654	ATATAGATAGACTTC[A/G]CTTACAAGGAAGCCA	9873
rs181380863	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72936750	TTGTATTTTTAACTC[A/C]AGAATTTATATTTGA	9873
rs181395072	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969184	AGCCATGTCAAAATC[A/C]GTGTTAACAGTCTAC	9873
rs181414633	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72904081	AGTGTGTAAAGGGTA[C/T]GAGAAGAGAACAAGG	9873
rs181421003	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73055241	TGGGGATTATGGGAG[C/T]TACAATTCAAGATGA	9873
rs181421111	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73028206	GGCACTCAATGGCAG[C/G]CTGTGAAAGTAGCTG	9873
rs181422098	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73104524	ATCCAGCCTCCCAAA[A/G]TGTTGGGATTACAGG	9873
rs181424075	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73072012	TTTTTTGATCAGCGG[C/T]CAGGGCAGGGGACTC	9873
rs181424154	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73010047	TAATATGTGTATTTG[G/T]TCACTTTATGTTGTC	9873
rs181426916	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72947976	ATAATTTTTATGACA[C/T]CGTTTGGGTATCATA	9873
rs181427267	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73034709	TTCAACTTCAATAAA[C/T]TTATTTGCACAAAAT	9873
rs181431934	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72991485	ACTGGCAAACCAAAT[A/C]CAGCAGCACACCAAA	9873
rs181432454	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73000713	TATTGTGAAACTAAG[G/T]AGATCTATGTACTTG	9873
rs181452832	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958421	TATTTGGGAGGCTGA[C/G]GCAGGAGAATCACTG	9873
rs181454747	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989743	ACACACCGGGGCCAA[G/T]CAACACTGCCTCAGG	9873
rs181477592	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73045019	AGGTTGCAGTGAGCC[A/G]AGATCGCTCCACTGC	9873
rs181477925	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72904790	TCATATACTAGTTTC[G/T]TCATCTATCTCTCCT	9873
rs181481128	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72918001	TTGGGGAATATTACA[A/G]TATTAGCAACATGAA	9873
rs181488848	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72980785	ATATACATCTCACTC[C/T]CTTCTACCATATTGA	9873
rs181490441	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73027435	AGCAGCAAAGCATTC[A/C]AAATGTAACCTGGCT	9873
rs181490623	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937411	AGCATTTAGCAAGAA[A/G]TATAAAGCCTTAGTG	9873
rs181496436	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132071	TCTGGGATTTTCTTA[C/T]AAGATTGCTGATACC	9873
rs181497343	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73009220	CATACTACAGGCTGG[A/G]TGTGGTGGCTCACGC	9873
rs181502117	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72865976	GTTCATCTTCAGTTT[G/T]CCCAGGAAGTAAGTA	9873
rs181505512	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083463	CTGACACAGGAGAAT[C/T]GCTTGAACCTGAGAG	9873
rs181515227	snp	A/G	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:72882030	GGCGCCTGTAGTCCC[A/G]GCTAGTTGGGAGGCT	9873
rs181527132	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73127207	AACACCAGAAATAAC[A/G]TTTTCTTATTAAATT	9873
rs181562425	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73017731	TTCATAATGCTCCCA[C/T]TGCATGAAAATATCT	9873
rs181574020	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978622	CTGGATTATAGGAGC[G/T]ATTTCCCTGATGCTG	9873
rs181590527	snp	A/G	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:73063313	TGGAAAGGAACAACC[A/G]GTACCAGCCACTGCA	9873
rs181624383	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72869728	AGAGATCAAGAGTGA[C/T]AAAGTCTGTTTCCTT	9873
rs181640042	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72885865	TTCATTGTACACCCT[A/G]CCCTCCTCACTATGG	9873
rs181660842	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73010979	TTGGTGGTGGCTGTG[A/G]GGGGGTGGGCAGCTC	9873
rs181667824	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72945890	TCATTAGAAAGTCAG[G/T]AAACAACTGGTGCTG	9873
rs181691094	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909796	AGGAGCACCTCTGCC[C/T]GGCCGCCCCGTCTGA	9873
rs181717233	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846783	TCATACATGTTCATC[A/G]TAGAAAAGCTGGAAA	9873
rs181721870	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72874480	CAGGTGCGAGCCACT[A/G]TGCCTGACCTCTAGT	9873
rs181728041	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73134456	GCTTGGGTGACAGGG[C/T]GAGACCCTGTCTCAA	9873
rs181759893	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73001533	ACTGAGGCCCAGAGA[A/G]ATTTTAGAGTATCAC	9873
rs181786694	snp	C/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73055737	ACAATCTGTAGAGTA[C/G]AAAAGCAGAAATATC	9873
rs181787878	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72889253	GGCGTGAGCCACCGC[A/G]CCCGGCTATAATTAT	9873
rs181793089	snp	G/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73018257	GTTCCTGGCCCAGAC[G/T]TGAAATAAGCTAGTT	9873
rs181799148	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092159	TAGAGGTAGGGTCTT[G/T]CTCCATCACTAAGGC	9873
rs181805737	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72996792	AACAAAATACATTTT[A/T]AAAAAACTGCCAGCA	9873
rs181817308	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925601	TTTGTTGCCACGGTG[C/T]ATTTCACTTCAGCAA	9873
rs181827318	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890232	TGGACTTATCTTTCC[A/G/T]AGTGGGAAGGAAGCT	9873
rs181831271	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936091	ACCACTTACTAGCAA[C/T]CATCACTCTGGGAAG	9873
rs181836447	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72955477	GCATAATTGGTTACA[C/T]CACTGGCTAATGGTG	9873
rs181837297	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72910435	TGTTACTGTGTCTGT[A/G]TAGAAAGAAGTAGAC	9873
rs181837962	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854489	CAAGCTGGAGTGCAA[C/T]GGTGCGATCATAGCT	9873
rs181839815	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72926394	GGCATGACCAGTTGC[A/T]GAGAGGAGTATTCTC	9873
rs181841793	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73094740	TTTATTATCAGCAAA[C/T]TGATAATTGTTTAAT	9873
rs181847422	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104016	AATACAAATAAATGT[C/T]TTCTGTTATTAAACC	9873
rs181855206	snp	G/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73074079	AGTACTTAAAACAGT[G/T]TGATATCGGGAAAAA	9873
rs181855299	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126668	TGTTTACCAATATTA[A/C]TGAATCATTAAATTT	9873
rs181924570	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72930840	GTAGGGATGGCTAAT[C/G]GGTACAAAAAAATAG	9873
rs181927956	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72900675	AAAAGCTGATTTGAT[A/T]AAAAAAAAAAAGCAC	9873
rs181928289	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73009514	AAACAAAGTCATACT[A/G]GAAAAAATTAAATAT	9873
rs181930369	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950930	TCTCTAATTCAGTGT[G/T]AACAGAAGTAACATT	9873
rs181938995	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73082484	AATTAGTTCTGTCTA[C/G]CTTTCAAGGAATAGG	9873
rs181948780	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894671	GTATTCCAACTACAC[A/G]TTTGTACAGGTTCAC	9873
rs181951898	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914248	TTGAACTCCTGACCT[A/C]AAGTGATCTGCCCAC	9873
rs181954327	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73046037	ATTTTGTCACCTAGG[C/T]TGAAGTGCAGTGGCA	9873
rs181961231	snp	A/G	0.000165645	0.00909918	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838819	ATTTCCACATCTTCA[A/G]TCTTCTCTGCTGGCC	9873
rs181968071	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73099021	GAGTTCAAAGCCAGC[C/T]TGGCCCACATAGTAA	9873
rs181974029	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877337	TTCAGGCCAGTAAGA[C/T]GGAGGTTCTGCTTAA	9873
rs181975849	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73059107	AAACAAGAAAATGAG[A/T]CTACTTTCAGTGAGA	9873
rs181976528	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72859677	AGAAGAGAGAGATGC[A/G]CAGAACTTAGGAAAT	9873
rs181976872	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72885242	GGAAACCAAGTGAGA[G/T]TATTTTATGCTAACA	9873
rs181978805	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73079246	CTGTTGCCCAGGCTG[G/T]AGTGTGGTGGCCTGA	9873
rs181984515	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72968648	TGATTTCCAAAATGA[C/T]AGTGCTGGCATGGAA	9873
rs182007133	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72986085	CCTCTTATTTTTCTA[A/G]CAAGAGAAAACATTC	9873
rs182020883	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73040895	AAACTGCTCCCCCCC[C/T]TCTTTGGTAACTATC	9873
rs182034340	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023252	CAAAGAGAATAAAAA[G/T]ACAAGCTGCAGATTA	9873
rs182039275	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005465	ACTTGGCTTCCAGGA[A/C]ATCACTCTCCCTTGG	9873
rs182046529	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035955	CAATCTCTTGACCTT[A/G]TGATCCGCCTACCTC	9873
rs182064182	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117962	ATATGCACACATATT[A/C]TATATACATTTTCTG	9873
rs182067434	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73073024	ATGTTTTCCTGCTCC[C/T]TCTCTCCAGCCACAG	9873
rs182083298	snp	C/T	0.0228947	0.104514	intron-variant	FCHSD2	GRCh38.p7	11:72850514	GCCCACCACCACGCC[C/T]GGCTAATTTTTTGTA	9873
rs182092878	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118595	CATAATTCACTCATT[C/T]TTATTGCTGAATGGT	9873
rs182094043	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73066395	AGGACCATAAAAATC[C/T]TAGAAGAAAACCTAG	9873
rs182098294	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73118861	ACTTACCCAAGGTCA[C/T]ACAACTAGGGGAAAA	9873
rs182102151	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73135868	AAGATAAGAACTGGG[A/G]ATTAAGGGGTGCGTT	9873
rs182145962	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72922069	TATTAATAATAAATG[C/G]ACAAAAGATACAGAT	9873
rs182153195	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72850758	TACTGACTGACAAGG[C/G]CCTCTAAATTTTAAC	9873
rs182166562	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886615	TGTCTACCTCCATAC[C/T]CCTTCACCACATTGC	9873
rs182204251	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72887154	ATATCTAAATTGATA[C/T]ATATACATCATTTTT	9873
rs182208123	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73027649	GAAGCCAAATGTTAA[C/T]AGCCAAAACAATGAA	9873
rs182222664	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73070264	GCCTCTTATATGGCA[C/T]AGGCCCTGTCTGCTC	9873
rs182232673	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73064117	CAATCAAACTAGAAC[G/T]CAGGATTAAGACACT	9873
rs182234585	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72908602	TGATATAATATCTTA[C/T]TGTAGTTTTGATTTG	9873
rs182243265	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72922594	GATTAAGCTATGATG[A/T]GTACTGTCACCAAAA	9873
rs182244532	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72946654	TATTGTGGAAGTATC[C/T]AGCATATTTTACCTT	9873
rs182249473	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997783	TCGACTTCCTGCAAT[C/T]TCTACCTCCTGTGCT	9873
rs182253972	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72975325	ATATATCCAGCAGTA[C/G]AGAGTAGATTGGTGG	9873
rs182254359	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72851588	TATTAACAAAAAAAC[A/T]AAAAATTAGCCGGGC	9873
rs182264940	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72870761	AAAAATTAGCTGGGC[A/G]TGGTGGCGGGTGCCT	9873
rs182265472	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72990093	TCTAGAAGATTCTGC[A/G]TGGACAGATAAAAGC	9873
rs182266336	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953398	TCTACATTTGGAAAA[C/T]AAATTCTCTCTCTTA	9873
rs182268551	snp	A/G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73032756	CTGTAACGAGAGGTG[A/G/T]GGTGCAAGTGGGAAC	9873
rs182268826	snp	C/T	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73053787	TTATGACTATAGCAG[C/T]GATTCTCTATATTAA	9873
rs182272751	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138992	TTAAAATTGTAATTT[G/T]CAGTCAGAAAACAAC	9873
rs182279750	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73014932	CAATGCAACCTCTGC[C/T]TCCCAGGTTCAAGCA	9873
rs182284608	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72967124	AGAATGGCGTGAACC[C/T]GGGAGGCAGAGCTTG	9873
rs182304489	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72964842	TTGCCCAGGCTGGAG[C/T]GCACTGGCAGGATCT	9873
rs182313755	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72994716	GCTTGCAGTGAGCCG[A/G]GATCATGCCACTGCA	9873
rs182320430	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73102950	ATACACAACATGGAT[A/G]AATCTCAAAAACATT	9873
rs182331082	snp	A/G	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73124259	ACACCAGGGCCTATT[A/G]TGGGATGGGGGGACG	9873
rs182374528	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135728	TTAGTTGTCTTTTCA[C/T]CTCAAACTTCACTCC	9873
rs182405550	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908311	GGTTGCTTCTAAATC[A/T]TGGCTATTGTGAATA	9873
rs182417969	snp	C/T	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72869363	ACAGATGCTAATTTT[C/T]CACTTGAAGCAGGGC	9873
rs182423745	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73107230	CAGCTAAGTTTTGTA[G/T]TTTTAGTAGAGACAG	9873
rs182424320	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72972540	ATAACTTCCCTTTTA[C/T]CTGCTTTATATATAA	9873
rs182429206	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72861160	AAACCTCTAGCAGAA[C/T]GATCAGAAGAGAGGA	9873
rs182430195	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72878168	GTTGTAGTCACAACT[A/G]TTTTGGAGGCTGAGG	9873
rs182436006	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870075	GCTTGCGTGCCTGTG[A/T]GCGTGCCAGTCCCTC	9873
rs182441899	snp	C/T	0.0437281	0.141251	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73142813	CTGCCTGCCTTTGCG[C/T]GTGTGTGTGTGTGTG	9873
rs182443796	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73133536	CCCAGCACTTTGGCA[G/T]GCCAAGGCAGGTGGA	9873
rs182456524	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112647	GCCTTTTTGTTGTTG[G/T]TGGTGGTGTTGGTGT	9873
rs182472858	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72943365	TTCAACTATAGTTAG[A/G]ATTAACTGAGGACTA	9873
rs182480660	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915674	AATACAAAAATTAGC[C/T]GGGCGCGGTGGTGGG	9873
rs182498339	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986740	AATCCTAATATACTT[A/C]TTGTGTAGTATTAAG	9873
rs182498829	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965299	TACTTGGAAAGTTCT[C/T]CATTTGCCTGTCTTC	9873
rs182509033	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72843767	CTCAAGAGGCAATGA[C/T]GTTCAATGAACAGAA	9873
rs182512810	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73088986	CCTTGATGTGCATAT[C/G]AACTAATTTAAATAT	9873
rs182518328	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73053928	AAAAATTTTAACCAT[A/G]TATTTTTTACTCATC	9873
rs182519872	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923342	ATTGCTCGGTCATAT[A/G]ATAACTCTATGTTTA	9873
rs182521085	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024235	ATCCAATTGTATTAC[A/C]AAATGTGAGACATAA	9873
rs182522258	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73070486	TGGAGTGCAGTGGCA[C/T]GACCTTGGCTCACTG	9873
rs182526176	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878905	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	9873
rs182528664	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943793	TGATATTTTATTAGT[G/T]CATTAACTACAAGAA	9873
rs182532144	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120938	ACATAGGCTCCCCAC[A/G]AAATCTAATCTGGCA	9873
rs182533272	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006972	TCTCAGTAACAATGC[C/T]GAACATTAAAAAGGG	9873
rs182538621	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72988002	ACATCAAGTCCTTCA[C/T]GAATACTCACTTACC	9873
rs182553797	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908892	CTCCTGGGCTCAAGC[A/G]ATCTGCCCACCTTGG	9873
rs182566801	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73012659	ACAATAGCACCACCA[G/T]CCTCTCAGTTGCCTA	9873
rs182573882	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088664	TTTTTTACACTCATG[C/T]TGTTTTTCTAAAATT	9873
rs182575915	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72872286	CTTTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT	9873
rs182580884	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72942396	TTATATTACCCAGCC[C/T]TGTGTATTTCTTTAA	9873
rs182584771	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72953628	AGACACTGCATGGGG[A/G]AAAAAAAAAACACAA	9873
rs182618666	snp	C/T	0.0162398	0.0886349	intron-variant	FCHSD2	GRCh38.p7	11:73133132	ATGCACTGGCCATGA[C/T]GTGGAGAAATAGGAC	9873
rs182644421	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074548	GGTGGACTTTAGGAT[A/G]GCAATATACCCTTAA	9873
rs182651788	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73050452	ATTACTATAAACATA[C/T]ATGGGACGGGTCACC	9873
rs182652041	snp	C/T	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73096356	GACCAGCCTGGCCAA[C/T]ATGTTGAAACCCTGC	9873
rs182661874	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085237	TTTTTTTTTAAATGT[C/T]TATTCAAAAAAAGTC	9873
rs182679253	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848556	TAACCCTTCATAGAT[C/T]GTCCATTCCTAGAGG	9873
rs182697946	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72910812	GAGAAACACCCAAGA[A/G]TGATCAATAAATACT	9873
rs182699348	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72867482	CACTTAAGATTTTGT[A/G]CAAATCTCTGGATGT	9873
rs182709180	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73129906	TTGAGACAGAGTCTC[A/G]CTCTGTCGCCCAGGC	9873
rs182723977	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72934214	TGAAGATGCATCTGT[A/C]TCTTGTCTAGCATTT	9873
rs182725545	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72999876	AATCAGACACACACA[C/G]ACACACACACAAACA	9873
rs182736697	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72899519	AGGAGGATCTTTTGA[A/G]CCCAGGAGTTCAAGG	9873
rs182752486	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72934418	TCACTGCAACCTCCA[A/C]CTCCTGGGTTCAAGA	9873
rs182761531	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72863208	TTGGGATTACAGGCA[C/T]AAGCCACTGTGGCAG	9873
rs182833308	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927060	TCCTAGTTTTTACTA[C/T]CTTAACAATTCACAA	9873
rs182833359	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883155	ATGACCCTTAACTCA[C/T]ACCAGACCTCAACAA	9873
rs182835402	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905603	AGCCCCCCACCCCCC[G/T]ACAGGTCCCAGTGCG	9873
rs182862047	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856121	TTACATTAATTAATT[A/G]AAGTATCAAATATCT	9873
rs182862834	snp	A/C/G	0.00119752	0.0244452	intron-variant	FCHSD2	GRCh38.p7	11:73111702	TTCCTTTTAGTGAAG[A/C/G]TGATTTTCTCTGGTG	9873
rs182866364	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72872131	TACGTCTTTATATAA[A/G]ACAATTGGAATTTTT	9873
rs182903177	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123679	ATACGATCTTCTTAA[C/T]TGCATAACCATCCCC	9873
rs182916806	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73081127	AATAATAAACATGTC[C/G]TATTTACTTGATTAA	9873
rs182923281	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73102102	TTCATTAAAAACTTA[C/T]CCAAATAATTGGTAA	9873
rs182954713	snp	A/G	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73080595	TCTCATTTATTATAG[A/G]TAATCAAGTGATAAT	9873
rs182963334	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73015676	AAATTTTGATAATTT[C/T]GAAATTATATCCGAA	9873
rs182967548	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72920113	TAAACTGTAAGACAG[C/T]AGAAATAATGAATAT	9873
rs182969082	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042221	TGCGCCACTGCACCC[A/G]GCTGAGATTATTTTT	9873
rs182971398	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73122460	TCCTGCACAAAGGTA[A/G]CACCACTTAACCATC	9873
rs182991888	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842452	ACATTCCACAAGGGA[C/T]TGACTGACAAGTCTC	9873
rs183007295	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891018	AACCTCCGGGCTCAA[C/G]TGACTCTCCCACTTC	9873
rs183045873	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73127824	TGGGTGCAGTGGCTC[A/C]AGCTGTAATCCCAAC	9873
rs183048980	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73084306	ACAAAACAATGTACA[A/C]GGCCACTACAAATTG	9873
rs183051783	snp	A/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72855644	ATGTAACACAAGGAG[A/G]ATAATTTTTTAACCC	9873
rs183056692	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73106361	CAGTGAGCTGTGATG[A/G]CACCACTACACTCCA	9873
rs183063407	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73002070	TCATCTCCTGAGATT[G/T]CCCTTTTGTGGGAAA	9873
rs183070081	snp	A/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72981467	CCAATAGAAAAAAAA[A/T]AGGATTTTATTTTTG	9873
rs183079493	snp	C/G/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72983288	GACAGAGCGAGACTC[C/G/T]GTCTCAAAAAAAAAA	9873
rs183084863	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72961676	TTTCAGAGCAAGTTA[C/T]TAAATATACTAGCCT	9873
rs183086221	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72912594	GTTTTTATTTTTTGA[A/T]GTGTCTTTGTCTGAT	9873
rs183087190	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010398	TTCCAGGATTTTGTA[A/T]ATTTGTTTTTTATTG	9873
rs183089634	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72959150	TCTGTCAATACTCTT[C/T]ACCCATTTTAGAAAT	9873
rs183093778	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037306	CATCTGAAGTCCATG[A/G]TTTACACTAGGATTC	9873
rs183096908	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018938	TATGAGGGTTCAATT[A/G]AGTCAAGATCTCAGA	9873
rs183100428	snp	A/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72949389	CTGGAGGCAGAGGTT[A/T]CAGTGAGCCGAGATC	9873
rs183105172	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72939295	TGACAGTAATTCCCC[A/C]CTAAAAATTGTAACT	9873
rs183106982	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73020217	TTAACAAGTGAAGAA[A/G]CACAAAGAGAGCCAC	9873
rs183107250	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876856	GCATTATTATTATAT[A/C]TACGTCCAGGATTTT	9873
rs183108949	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73065307	GACAAAATTAAACAG[C/T]GCTTCATGCTAAAAA	9873
rs183110218	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73037677	GTGGCCATTTAATCA[C/T]ATAAGTCAGATATAG	9873
rs183114142	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73002890	TAATTGTTTATTAAC[A/G]TCTGTCCCTCTCACT	9873
rs183114198	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72856708	ATCATCAGTCAGTTC[A/G]GTGGCAAAACAGTCT	9873
rs183117270	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047528	AATACTGGTCATTGA[C/T]AGTACCTAGCCACTG	9873
rs183117431	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028794	GTCTCATGATAGTGA[C/G]TTCTCATGAGAGCTG	9873
rs183123969	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002576	ACTATTAATTTATAC[A/T]TAAAATACATTTTAA	9873
rs183129175	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72893474	CATATGCCATCACAC[A/G]CAGATAATTTTTTTG	9873
rs183129847	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72888124	AATAAGAAAACAAGA[C/T]AGCCAAGTATAGGAA	9873
rs183170315	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72851825	CTCAATATCACTAAA[A/G]AAATGCAAATCAAAA	9873
rs183172658	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72960352	GATCACATTTCAACA[C/T]GCAATTTGGAAGAAA	9873
rs183174428	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843387	TAGACAGGGCACAAC[A/G]AAGACCAAAACAAAC	9873
rs183209096	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73056405	GAACACTGCTCATAC[A/C]CCCAAAATGTAATCT	9873
rs183224290	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72919253	CTCTTCTGGTACTTG[A/G]AACAAAAGGGCACTA	9873
rs183226014	snp	A/C	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73032920	AATCAAGCTTGCGAG[A/C]AGTGCAGTGCCATTA	9873
rs183242385	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73061412	CTAGCTGCAGGAATT[A/C]TTTTTTTCCATACCC	9873
rs183244284	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72861737	GAGTTCAAGACCAAC[C/T]TGACCGACATAGAGA	9873
rs183249206	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878282	GAAATATATTGAGAC[A/C]CTGTCTCTAAAAATA	9873
rs183251833	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998697	TAGTGGAGGAAAAAA[A/T]TGATAATAAAAAATA	9873
rs183262581	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898865	TTCCTGAGTAGCAGG[A/G]ACTACAGGTGTGTGC	9873
rs183266272	snp	A/G			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140212	TACATCTGTCAGAAT[A/G]TGTCTCTTGCTCGCC	9873
rs183270202	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73099836	GAGAGGCGGCACCAC[A/C]ATTTTCTTCCCACCT	9873
rs183283548	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875583	ATCCTTCCGCCCTCC[A/T]GCCCTGGCCTCCCAA	9873
rs183300556	snp	C/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73129501	ACTGCACATGCAAGG[C/G]ATCTAGGTTGCATGC	9873
rs183317811	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73141150	AGCGGGGAGACTGAT[A/G]ACAAGCCGGGTGCAT	9873
rs183343329	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72948373	TCAAAATTACTGAAT[A/G]TTTCATTTTTCAACA	9873
rs183351214	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72876443	GCAGCAACAGATTAC[C/T]GTGTTTGAACAACAT	9873
rs183373687	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72911073	CTTTGCCTAGTCCTA[C/T]GTCTTAGAGAGTTTC	9873
rs183376673	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73019465	CTATTTTTTTAAATT[A/G]TGAAATTAATTTGTT	9873
rs183420678	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72938559	TTTGCAAGGTGTCCT[C/T]TTCCTGACTGAATGA	9873
rs183442868	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72915158	AAAACTCAACATCAC[C/T]GATCATTACAGAAAT	9873
rs183444141	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72982420	GTGTGTGTTTGTTAG[A/T]CATTAAGAACAATAC	9873
rs183446404	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72933861	TGCCTGCAATTTCAA[C/G]ACTTTTGGAGGCTTA	9873
rs183448004	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72975006	AAGATGAGTTATATA[C/T]GCCTACATATGAATG	9873
rs183453164	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73057136	CATAGGTTGACAATT[C/G]ATTTGCATCGTGAAG	9873
rs183453698	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72952782	AGGCACTTACACATA[C/T]TTACAATTCATGAAA	9873
rs183477087	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73096631	TCAAACACAAGAGAA[C/T]AGCAATGGTAAAAAG	9873
rs183480670	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73136247	AATTCTATTTACAGT[C/T]TAATGTGCTGTAGAT	9873
rs183496026	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024687	ATCAAAAGAAACTAT[C/G]AACAGAGTAAACAGA	9873
rs183499592	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72991987	TCCCTGTTTGTAGAT[A/G]ACATGATTGTTTATT	9873
rs183503641	snp	G/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73007495	AAGCATGGTGGTAGT[G/T]GTGGCTATGCAGGAG	9873
rs183514223	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061861	CAGAGCACTTGGGGA[A/G]AGGGGCAGCTGTGGG	9873
rs183523300	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73043309	ATCACTAAAAGGCTC[A/G]GTCAAGTAGTGAAGA	9873
rs183547931	snp	C/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72853447	GGAGACAGAGTCTCG[C/G]TCTGTTGCCCAGGCT	9873
rs183560554	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72888914	GGCGTGAGCCACTGC[A/G]CCCAGCCAAACATAT	9873
rs183573794	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72927995	CATTTATAATTAGGG[A/C]AAGTGGGAGTACCAC	9873
rs183602278	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892067	ATCTCAAAGAGAATG[A/G]ATTTGTAGGGAGTAG	9873
rs183603895	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137231	GAAACCTAAACTCTT[A/G]TTTTAGTAGGTAATA	9873
rs183666875	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011422	GCCCCAGCACCACTC[A/G]CTCCCCAGCAGCACT	9873
rs183679967	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72970328	ACAATCCAGTGAGTA[A/G]AAATACTTACAATTC	9873
rs183682027	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73120590	CAAAATTAGCCGGGC[G/T]TGGTGGTGCATGCCT	9873
rs183684314	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075083	ATCATCAGGAAAGTG[C/T]AAATCAAACCCACAA	9873
rs183686924	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72909209	GCCTGACTGGTTTTT[A/G]TATTTTTGGTGGAGA	9873
rs183690873	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73098426	CTTTATATGATTTTG[A/G]TCTTTTAAAATTAAC	9873
rs183692622	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72924524	CCTGATCTCGTGATC[C/T]GCCCACCTTGGCCTC	9873
rs183693329	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72905481	TCTAGGGTACATAGG[C/T]ACAACGTGCAGGTTT	9873
rs183699941	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73038579	GCAACGATTATCCTA[A/G]GCAAACTAACACAGA	9873
rs183703429	snp	C/T	0.0498117	0.149749	intron-variant	FCHSD2	GRCh38.p7	11:72944384	TCAATAAATTAGGTA[C/T]TGATGGGACGTATCT	9873
rs183714081	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72937819	CCTAGACAAACATGA[A/G]GTTTAAAAATGATTT	9873
rs183725018	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73119962	CAGTTCCACATGGCT[A/G]GGGAAGCCTCACAAT	9873
rs183746625	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72969365	ATTAGAACTGTGCAG[A/G]AAAGCTAGTTGGCAT	9873
rs183749768	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72866910	AGTTGGGAGGTTAGA[C/G]TTTTAGCTTTTAGTT	9873
rs183778210	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73017245	TGTCCTCCCAAAGTT[C/T]TGGGATTACAAGTAT	9873
rs183787235	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72999663	CAGTTAAATTCAGGT[C/T]TGAGATTACTTCATC	9873
rs183792793	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978359	AAAATAAAAATGAGC[A/C]AAAAATCTGAATAGA	9873
rs183812781	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72925257	CCTTACCATAATCAG[A/G]ATCATTTCTGATTAT	9873
rs183818421	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048315	TACCTCTGATCTCCC[C/T]TAAGCCAAGGTTCAT	9873
rs183821478	snp	A/T	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72944939	TTCCATGCTCACGGG[A/T]AGGAAGAATCAATAT	9873
rs183830121	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73071560	AAAAAAATTAGCTGG[A/G]CATGGTGGTGTGTGC	9873
rs183834907	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055058	AAAAGGAGGAACAAA[A/G]GCTCATCCTACCTGG	9873
rs183838938	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034106	TTATACTTTAAGTTC[C/T]GGGATACATGTGCAG	9873
rs183875624	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084683	ACTGGCATGGGCCAA[C/T]GTGCTTAGCCAGTAC	9873
rs183894886	snp	C/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72992508	CCTGACTTCAAACTA[C/T]ACTACAAGGCTACGG	9873
rs183914914	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72918478	ATGTTAGCAGAGGAA[G/T]ATTTCAGTCTTTCAT	9873
rs183940938	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72959220	CATATATCCAGCAGT[C/T]TTTTTTTTTTTTTTT	9873
rs183941106	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72847581	AAAGCAGTACTATAT[A/G]AAAGGACATTTTTGT	9873
rs183946797	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73091367	AACATGGTGAAACCC[A/C]ATCTCTACTAAAAAT	9873
rs183947373	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989448	AAAGAATAAGGCAAT[A/T]CTGTATTTCCCCATA	9873
rs183949153	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72882238	ATGAGGTCAGGAGTT[C/T]GAGACCAGCTTGGCC	9873
rs183957437	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72967882	GGATCACGAGGTCAG[A/G]AGATTGAGACCATCC	9873
rs183978829	snp	C/G	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:73044847	AGGCCGAGGCAGGTG[C/G]ATCACGAGGTCAGGA	9873
rs183979932	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73027060	ACCGAGAGACATGGC[A/G]TATTTCTATAAAAAT	9873
rs183983718	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008971	TAAGCTTACTTAAAA[A/G]TCATTAGAGAGCTGA	9873
rs184004249	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900518	TGTGGAAAATAGCAA[C/T]GATAAAATAACATCA	9873
rs184009962	snp	A/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73032397	CCTGGTTAATTTTTT[A/T]AATTTTTTTATAGAG	9873
rs184011946	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73065852	CTCAAGGAAATAAGA[C/G]AGGACACAAACAAAT	9873
rs184017080	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029234	GAAAACAAAAGATAC[A/G]GAAACCACTTACAAG	9873
rs184017366	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72844000	GCAACAGAGCGAGAC[C/T]CTGTCTCTAAAAAAA	9873
rs184030487	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106476	CTCTTAAATCAGTAT[A/T]CTGCTTGTTAAAGAA	9873
rs184038970	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879551	ACATGAAGATAAATA[A/G]GAATGAACTAGAAGA	9873
rs184039673	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72863891	GTTGATGTAATTGTA[A/C]AATGGTATAACCACT	9873
rs184043683	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:73069352	ACAAAATAACTATCC[A/G]AAGAGAAATTTAAAA	9873
rs184050819	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923776	GAAACCCCGTCTCTA[A/C]TAAAAATACAAAAAT	9873
rs184061634	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72864611	TTGTCAATTAAAAAA[A/T]AAATAAATAAGAGTA	9873
rs184077037	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965784	TGCATGTTCTTAAGT[A/G]TATAAATAGAATCAC	9873
rs184080953	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72996912	TGTTTTTCCTTAGGG[C/T]ATTTGTTGAATCATG	9873
rs184085547	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72994333	CAGGTGCTATGTTTC[A/G]TACTTTACAGGTATT	9873
rs184090852	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72888535	ATAGGTATCAATAAA[C/T]GAAACAGAAAAAAAG	9873
rs184095645	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971744	GCCAAGGTGACATTT[C/G]GATTTTGGCCTTGTG	9873
rs184100530	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73116256	CCCAATTTCATTATT[A/G]CTTAATTTTCTTATA	9873
rs184105479	snp	A/C	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72949408	TGAGCCGAGATCATG[A/C]CACTGCACTCTAGCC	9873
rs184109355	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921374	GCTGTCAAAGAATGA[C/G]AGCATATAGATAGTA	9873
rs184115010	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091904	AAATTAGCTGGTAGC[A/G/T]TGCACCTGTAATCCC	9873
rs184117614	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73029986	AATCTGATGTCCAGA[C/G]TCACCACCTTATTAG	9873
rs184118909	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73011847	TTTCCTGTCACTTTT[A/C]TGTTGAATTCCAGTG	9873
rs184135260	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885302	AAAACTGAGAAAACG[A/G]ATCTGCTACAATGGT	9873
rs184135454	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72929584	CCTGCCTTAAATTGC[A/G]ATTGTCTGAACCAAT	9873
rs184138637	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907342	CTTTCTCTTGCCTGA[C/T]TGCCTTAGCCAGAAC	9873
rs184154871	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052728	TTTTAATAATCTTCA[C/T]ACTTGTAAGAAAGGG	9873
rs184156001	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850367	ACTGCACCAGGCCTA[A/G]GACAGAGATTTTTTT	9873
rs184166241	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988067	ACAAGTTGCTTATAA[A/G]GTTGCTTACATTTCT	9873
rs184170588	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014800	GGACAACTCCTGAGC[A/G]TAAAAGATAATAAAT	9873
rs184171222	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73040415	AAACACATACACACA[C/G]ATACACATTTGTATG	9873
rs184185068	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126057	AAGACAAAAGAATTC[C/T]ACGGCCAGGTGCGGT	9873
rs184195207	snp	A/T	0.0205511	0.0992634	intron-variant	FCHSD2	GRCh38.p7	11:73087719	CAAAAAAAAAAAAAA[A/T]ATTTTTAAAATAAAT	9873
rs184198940	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73077225	TAAGAAACCAAACAA[C/T]CCAATTTAAAAAAAA	9873
rs184212589	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943916	ACTATTAAATACTCA[C/G]ACTTTAATCATTATT	9873
rs184213415	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045854	AGCCACCAGCATGGC[A/T]CATGTATACATATGT	9873
rs184216272	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027574	CCATGAGGTAGAAAA[G/T]AAAAACCAATTTTCT	9873
rs184231701	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134310	ACCCTCTCTCTACAA[A/C]AAATACAAAATTAGC	9873
rs184234438	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73082164	AACAGGGTGAAACCC[A/G]GTCTCTACTAAAAAT	9873
rs184235898	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72872464	GCCCCCTATTCCCTG[C/T]AGTCTTGACAATCAC	9873
rs184237359	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73103174	GTGTAGTAGTGTTTA[A/G]TCAACTACATATAAT	9873
rs184243700	snp	A/C/G	0.00279242	0.0372774	intron-variant	FCHSD2	GRCh38.p7	11:72909059	TCCCTTCCCCTCCCC[A/C/G]CTCCATCTCTCCGGT	9873
rs184244757	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72846244	GGAGTGCAGTGGTGC[A/C]ATCTCGGCTCACTGC	9873
rs184247422	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73063386	CTGCATCAACTAATG[A/G]TCAAAACAACCAGCT	9873
rs184254412	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72938183	ATGAAGGAGTTTTTT[G/T]TTTTTTTTTTTTTTT	9873
rs184306165	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058390	TGTGACATGGTATGG[C/T]TAGATGTCATCACAA	9873
rs184314338	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73021923	AAATAATAAAAAAAA[A/T]TTTCCAGGCCTGGTG	9873
rs184358381	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73062611	TGACCCGATGGAGCT[A/G]AAATACACAGCACGA	9873
rs184367755	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73040892	CACAAACTGCTCCCC[C/G]CCCTCTTTGGTAACT	9873
rs184371163	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023192	AAGAAAAATGATAAA[C/T]TGGACCTTATCAGAA	9873
rs184373248	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73025777	CTTATGACTAAGAAT[G/T]TTTTTAAAGCTATAT	9873
rs184374741	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051256	GGGGATTGAGGCTAC[A/G]GTGAGCCAAGATTGC	9873
rs184379086	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73066677	AAAGTAGGCAAAGGA[C/T]ATGAACAGACAGTTC	9873
rs184380496	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72865051	TTCCTTCCTTATTCT[A/G]TAAGGGAGTAGTCTG	9873
rs184399276	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72916835	TACTTGTGCTTTCAA[C/T]GTCAAATCTGAGAAT	9873
rs184415678	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956136	TGGAGCAATTTGAGC[A/G]TAAAAATAAATAGTA	9873
rs184431474	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881564	AGGAAAGGAAATCAG[C/T]GTATCAAAGTCATAC	9873
rs184437641	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883702	TCTGGGCGGCCAAGG[C/T]AGGCAGATTGCTTGA	9873
rs184438309	snp	A/C	0.000222796	0.0105522	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72989034	AGTATTTCTTTTTGC[A/C]TTTAGCTAAATCTTT	9873
rs184449954	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838272	GTTTCACTTTCTCAG[C/T]CTGGGGACTAACCTT	9873
rs184452452	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72877076	TCCAGGCTGCCTCCA[G/T]TGCAGCCTCATCCTC	9873
rs184454535	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72906148	TGACATAGTATCTCA[C/T]TGTGGTTTTGATTTG	9873
rs184457700	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858841	AAGATGGAGTATCAG[A/G]GATCAGATTTAACCT	9873
rs184478726	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73108137	TATCTCATTGTAGTT[C/T]TGATATGCATTTCTC	9873
rs184487789	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130472	ACCATCAAGTTCAGG[A/G]GAGTATCCTCTATTC	9873
rs184515736	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134127	CTCTAGACCAGATTA[A/G]ATTACCTCTAAGATC	9873
rs184516482	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081306	GGGCATGGTGGCACG[C/T]ACCTGTAGTCCCAGC	9873
rs184536470	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936335	GCTCTAAGTCTGTTA[C/T]CTTATCTATAAAATA	9873
rs184549370	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73008799	GAATTGTGAAAGAAA[C/T]CACATGCAAACAAGC	9873
rs184552304	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72934961	CTTTAAGCAGCCACG[A/T]CCTTTCCAGGTAGCT	9873
rs184558868	snp	C/T	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72909440	TGCTAAGATTACAGC[C/T]TCTGCCCAGCCGCCA	9873
rs184570692	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72903371	ACAGGCGCCCGCCAC[C/T]GCGCCCAGCTAATTT	9873
rs184575778	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967392	TGGGTAAACAAAATA[C/T]GGTATATCCATATCA	9873
rs184579057	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977341	GGACAAATGGGATCA[C/T]ATCAAGTTAAAAAAC	9873
rs184593267	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72874116	AATTTAATGTGCCTA[A/C]GTTTATCTTTTAACA	9873
rs184633554	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73115452	TGAGCCACTGCGCCC[A/G]CCCTATCTCACTGTT	9873
rs184668340	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:73082103	AGCACTTTGGGAGGC[C/T]GAGGTAGGCGGATCA	9873
rs184687037	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124853	AGATAATTACAGACA[C/T]TATACTAGTCACATT	9873
rs184690454	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72954371	ATGCCACCATGCCTG[A/G]CTAATTATTTTATTT	9873
rs184717545	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854051	TTAGGATGCTGTTAT[A/G]TATATTTTTAAAAAC	9873
rs184719227	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915860	AGAAAATGTGGTACA[C/T]ATACACCACAGAACA	9873
rs184720749	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72845478	AACAACAAACAAACA[A/C]AAACCATGGAGGTCC	9873
rs184723847	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852175	ATTATAGGAGTGAGC[C/T]ATCATGCCTGGCTGA	9873
rs184727292	snp	A/G	0.0256215	0.110247	intron-variant	FCHSD2	GRCh38.p7	11:72889080	CTGCCTCAACCTCCC[A/G]AGTAGCTGGGACTAC	9873
rs184731307	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72895424	CGTCTAACACTTTTG[A/G]GAACATACCTAGAGG	9873
rs184740279	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914303	TACAGGTGTGAGTCA[A/G]GTGCCCAGCCTGCCC	9873
rs184802273	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102988	AAAAGCAAATTACAC[A/T]ATTAAGTAGAAAATG	9873
rs184807794	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73063092	AACAGTGGATGTCTC[A/G]GCAGAAACCCTACAA	9873
rs184814935	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144332	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	9873
rs184817678	snp	A/G	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73120397	ATGTCTCATTTGGTA[A/G]CAAACATTTCTTCAG	9873
rs184834026	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73097368	GGTTTGTTTGTTTGG[C/T]TTATTTTATTTATTT	9873
rs184856359	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72899759	AAAAAAAAAAAAAAA[A/G]ACTTTTTAAATGATT	9873
rs184858202	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72966179	AGCCTTTTTTTTTTT[C/T]CAGTTGGTCTCACTC	9873
rs184871103	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73021261	AAACAGGCACACATA[C/T]GTTCACTGCAGCCCC	9873
rs184871339	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72973142	GGAGGCCAAGGCAGG[C/T]GGATCACCTGAGGTC	9873
rs184875062	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73003370	TAAATGAATACATAG[G/T]AACAGCAGCAGAATT	9873
rs184884281	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72984288	ATAGGAATCCTACTC[C/T]TAGTTTGCAATTAAT	9873
rs184892323	snp	G/T	0.0360663	0.129354	intron-variant	FCHSD2	GRCh38.p7	11:72931272	ACTAATTTTTGTGGG[G/T]TTTTTTTTTTTTTTA	9873
rs184895297	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057947	TGCAGTGGCACGATC[C/T]TGGCTCACTGCAAGC	9873
rs184898790	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076696	AATGGTATGTAAATT[A/T]AAAGTATACATAAAA	9873
rs184900038	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837690	TGTGCAGGGTGCGCA[A/G]TCCTTCAGTCCTTTC	9873
rs184901859	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72951408	CAGCAAACGAGAGCG[A/G]CAGATTACGCAGCTC	9873
rs184909189	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72994751	AGCCTGGGTGACAGA[A/G]CGAGACTCCATCTCA	9873
rs184913275	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73038764	TACCTGGGTGATAGA[C/T]TCATTCATACTCCAA	9873
rs184924083	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962988	CACTTAACTGCTTAC[C/T]TGTGTGAGCTGGCAA	9873
rs184924455	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73139972	CCTGGGGCTTGGTAA[C/T]TCAAAGGTTCTTTGA	9873
rs184927960	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122233	GTGATTCAAATTTTA[C/T]GTTTTCATCAAAGAA	9873
rs184930770	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72893702	GCAGTGAGCCAAGAT[C/T]GTGGCACTGCACTCC	9873
rs184952171	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72857989	GACCTCGTCTCTCTA[A/G]TGAAGACAGTTACTT	9873
rs184957157	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72896763	ATTAGGGGGAAAATA[A/C]TAAAAAAAAAAAAAA	9873
rs185013639	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72977964	GTGGCATATACACCA[C/T]GGAATACTATGCAGT	9873
rs185022919	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72984930	CTGGGAGGGAAAGTT[C/T]CTCCCTGAGTCAGTG	9873
rs185024886	snp	C/T	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72940626	GGCTCCCCGCCCCAC[C/T]CAGCCTGATAAAGCG	9873
rs185025525	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071220	TTCCTAGTTTTGCAC[C/T]TCAGAGTTACAAAAA	9873
rs185045639	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009291	ACTTGAGATCAAAGA[A/G]TTTGAGACCAGCCTG	9873
rs185045994	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913694	ACTTCTGATTTTATT[A/T]ATTTGGTTATTCTCT	9873
rs185050390	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955147	TCCCCACTTCAGATG[C/T]TAATTGGAAGTCTCA	9873
rs185058316	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999291	TTCACAGACATGAGC[A/G]TTTGTTGAATCTTAC	9873
rs185064989	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72880591	CCATATATAAAAGTC[A/G]GCTCAAAATGATTAA	9873
rs185066689	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73113522	TACAAGCATGTGCCA[C/G]CACGCCCAGCTAGTT	9873
rs185079300	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902737	ATTTTCTATACAAAT[A/G]AGAAATCATCCAACA	9873
rs185081423	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916379	CAGTAGTAGCATGAT[A/C]ATAGCCTGCTGCAGC	9873
rs185081838	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876876	TCCAGGATTTTAATA[C/T]ATTCATGATGAAATG	9873
rs185115877	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72849056	TTACCAAACACTGCC[A/G]CCTTTTGGCTACACA	9873
rs185127415	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73086238	ACATGGCAAAACTCC[A/G]TCTCTACTAAAAATA	9873
rs185142470	snp	C/T	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:73090514	ACAGGCGTGAGCCAC[C/T]GCGCGCGGCCTACAA	9873
rs185156277	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054643	GGGAAACAAACAGAG[C/G]GGGTGGAGGAAAGAG	9873
rs185161814	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73134029	ACTTTAAATGGGATA[C/T]GTAATCATATATGAT	9873
rs185174319	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73135773	CAAATGCCATTCGCA[A/G]AACAAATGAACTGAA	9873
rs185174560	snp	A/G	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72965111	TTACTTCTTAATTCA[A/G]AGGTCTTTGATAGAT	9873
rs185174791	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73013088	GAAACATTTCAACAC[C/T]TCCATTACGTTCTGA	9873
rs185180048	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73030434	ACATAAATGTATCCA[A/C]GTGAGTATATAGTTT	9873
rs185180656	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995248	AGCTGTTTTCCCCCT[A/C]AATTGTAATAGTACT	9873
rs185187404	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118711	AGAATATGATGATAC[C/T]ATAATGATGATGGCA	9873
rs185191355	snp	C/G	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:73068363	GGTAGGGTGGGGTTG[C/G]GGGGGCGGAGAGAGA	9873
rs185197764	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943548	TTAATGAAAGGGAAG[A/G]AAATTGAAGAGAATG	9873
rs185203016	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73058841	CCAAAGTGCTGGGAT[G/T]ACACGTGTGAGCCAT	9873
rs185209328	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031463	GTGACAGAACAAGAC[C/G]CTGTCTCCGAAAAAA	9873
rs185211439	snp	C/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73051919	CACACACACACACCC[C/T]ACACACACTGACATC	9873
rs185227205	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72868329	CATGAGTGGGGGAGA[A/C]CAACACACACTGGGG	9873
rs185227959	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950202	TGGGTTATTTGTTTT[C/T]ATTGAATTGTAAAGC	9873
rs185231884	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037389	ATTACAGTATCATAG[A/G]GAGTTATTTTCACTG	9873
rs185232170	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73019058	AAAATGTGATATAAG[C/T]ACCCAAATGAGGAAA	9873
rs185242099	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73002092	TGTGGGAAATCCATA[C/T]CGATTTTCAACCACA	9873
rs185244449	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73126978	GGGAGGCAGAGGTTG[C/T]AGTGAGCCGAGATTG	9873
rs185253195	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73095575	TGGACATATAAGGGA[A/G]TGATATGCTATAAGG	9873
rs185260595	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72914000	TAAAAATGGCCATAC[C/T]GCCTTAAGCTATTTA	9873
rs185261136	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056417	TACCCCCAAAATGTA[A/C]TCTTTTTAAAAATTA	9873
rs185262735	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73074177	CTAATGTGCCACAAA[A/G]TATCACTTCAATACA	9873
rs185280509	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72865685	TTTCTTCCCTATTCT[C/T]CTAGCTGATATTGAG	9873
rs185284915	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72881699	AATACTATTCAGTCA[C/T]AAAAAAGAATGAAAT	9873
rs185288665	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72904141	GAGATGAGGTGAGGA[C/G]TTGTCAGAATATGGT	9873
rs185308055	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72846702	GACAACCAGAGCTCC[A/G]TTTCCACCAGTATCT	9873
rs185319571	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72968709	TTGGCAGGGTTAAAG[C/G]CTATAAACTATATAC	9873
rs185339880	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72926428	GCTAATAGCTGGAGA[C/T]GATGGGATGGCCAGC	9873
rs185345917	snp	A/C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72947051	CCAGGTGAGATTCAG[A/C/G]TCCAAGAAAATGAGA	9873
rs185346335	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138744	TCCTGAGTAGCTAGG[A/G]CTACAGGCGCACGCC	9873
rs185359870	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72894179	GGTTGTTAGGCCAAT[A/G]GCATAACATTCTAGT	9873
rs185369923	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72972080	AAGAGTTAATCTCTT[C/T]AAAATTTTCTTCTTA	9873
rs185375011	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72890274	GCAAAGAAGAAAATG[C/T]ATTCATGCCAACCTA	9873
rs185376843	snp	C/T	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72939763	AGCTGGGATTACAGA[C/T]GCCCACCAAGACACT	9873
rs185377466	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72910666	TCCCTAATCTCAAGT[A/G]CCCAGGGATACAAAC	9873
rs185384171	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930364	GTTCTTTGTACATAC[C/T]GAAGATCACCCAATC	9873
rs185398608	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72869185	GTGCTGGGATTACAG[C/G]CATGAGCCACCTCAC	9873
rs185403435	snp	G/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72875365	CTATCTATCTATCTA[G/T]CTAGCTATTATTTAT	9873
rs185405508	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854777	CAGAATGGTGATTGT[C/T]AGAGGCTGCATGATG	9873
rs185411176	snp	C/T	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72906904	ATTGTCTTGGCTATG[C/T]GGGCTCTTTTTCGGT	9873
rs185461789	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73078823	TCCTGGACTCACGTG[A/G]TTCTCCTGCTTCAGT	9873
rs185463215	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73086044	AAGAAAACTATGTGC[A/G]GGCAAAATGTAAATA	9873
rs185471573	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73051589	GAAATAAAGACCAAC[A/G]ACTTTATACTATTTT	9873
rs185475769	snp	A/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73120729	AGCAAAATTGTGTCT[A/T]AAAAAATAATAATAA	9873
rs185484148	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73130790	CATAATATGGAAGTA[C/T]ATATTTACATTTAAA	9873
rs185494271	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72920836	AAAACAGATACATGA[C/T]AGGACTTCAAAGCAC	9873
rs185517797	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72962334	ACTTGGGCATTCTTG[C/T]GTCTCTAAATTTTCT	9873
rs185521083	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72884028	GTGACTAGCACTTGG[C/T]AATTGCAAAGAGGAA	9873
rs185540483	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73012840	AACAAATTTGACAAA[C/G]ACAAAAAACAAAACT	9873
rs185560266	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72849637	CTGTTATGTTGCCCC[A/G]ATATTAACCTAATAA	9873
rs185591246	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73067007	CCAAAGGATTATAAA[C/T]CATTCTACTATAAAG	9873
rs185599085	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73136921	TGGTGGCAGCTACTA[C/G]GGAGGCTGAGGCAGG	9873
rs185602991	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72861950	AAAAAAAAAAAAAAA[A/G]ATAATATATCATTAC	9873
rs185610794	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73028569	TGGGATAATGTTGGC[A/G]TGAGTTAAGACTTTG	9873
rs185612500	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010332	GTACTGTTTTTCAGA[A/T]TTTTCTTGTATCTCA	9873
rs185622050	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72991536	GTGGGCTTCATCCCC[A/G]GGATGCAAGGCTGGT	9873
rs185632386	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064973	AACTATTCCAAACAA[C/T]AGAAAAAGAGGGAAT	9873
rs185646571	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73072452	TTTAATGAAGTTTTT[A/T]AAAACTTAAAAATCA	9873
rs185654100	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047171	TACCAAACATGACTG[C/T]AAATTTGAAAAAAAA	9873
rs185663457	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031044	TAAAAAAAAGGGAGA[C/T]CCTGCTATTTGTCAC	9873
rs185668357	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72948171	TGCCACCAGACCTGG[C/T]AAATTTTTGTATTTT	9873
rs185681239	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72969193	AAAATCAGTGTTAAC[A/C]GTCTACCTACTCCCT	9873
rs185682464	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73033262	CACTGCACTCCAGCC[C/T]GGGCAACAGAGCGAG	9873
rs185689078	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72968143	TATAAGGCCTTTGGA[A/G]TTATCTTGAGGTTTT	9873
rs185722185	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73001664	TTATATAAACTGACG[C/T]GGCTGGAAAAATATA	9873
rs185730415	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980786	TATACATCTCACTCT[C/G]TTCTACCATATTGAG	9873
rs185741147	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864230	GCAATAAAAGAACAG[A/G]GTGGGCATAGTGGCT	9873
rs185746541	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958734	GTTTTATCTATAGTC[A/C]CTTAAAAGTAATCAG	9873
rs185755875	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080077	GCTGAGACAGGAGAA[C/T]TACTTGAACCCAGGA	9873
rs185767575	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73018529	TGTCTTTTTTTTTTT[C/T]TTTTAATCATTATAT	9873
rs185773315	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73042029	CTTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTTG	9873
rs185777114	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73109112	CTGTTTTTATGCCAG[C/T]ACCATGCTGTTTTGT	9873
rs185798316	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72887312	ATGTACTGCCTTCCA[A/C]AGAGCAGGTACTCAA	9873
rs185813870	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952570	CCTCAAGTGATCTAC[C/T]GGCCTCGGCCTCTCA	9873
rs185815472	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72908814	TATGCCACTATGCCC[C/T]GCTATAGTTTTGTAC	9873
rs185816183	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989915	CAGCAAAGCAGGAGG[A/G]GACACTGGTGAAGGA	9873
rs185819478	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73016434	TGTCTCCATTTTTAG[C/G]AAAAGGGTGAGTATA	9873
rs185820432	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72922769	TCTTGCCAATCAGTA[A/G]AGGTAAAAATTGAGG	9873
rs185824047	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974270	AGCAGAAGAGCAACA[A/G]AACACAAGAGGGAAA	9873
rs185847604	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006709	GCTTACTGCTCTTAC[C/T]GCCAATTGGCATATA	9873
rs185865193	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844866	AAAATCCAGATTCTG[A/G]ATGTTGCCATAGCTC	9873
rs185868512	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73005175	AAAAATCTCCATCAA[A/G]CCTCCATTTCTCACC	9873
rs185879396	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72985454	AGACTATTCTCAGTA[C/T]CATACAACTTCATAC	9873
rs185886891	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72964639	CAGCAGAATCTTCTG[C/T]GTTAACTTCCGAATC	9873
rs185893609	snp	A/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:73131314	CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	9873
rs185907639	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73060898	TGAAACCAGGCACTA[C/T]AGTGAGATTCCCGTG	9873
rs185907791	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837460	AATTTGATTTCTTAA[A/C]CAAGGAAAAAAAAAA	9873
rs185914978	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72907739	GGGACTACAGGCACC[C/T]GCCACCACGCCTGGC	9873
rs185923414	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878190	AGGCTGAGGCAGGAG[A/G]ATCATTTGAGTCCAG	9873
rs185923904	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106387	CTCCACCCTGGGTGA[C/G]AGAATGAGACTCTGT	9873
rs185924623	snp	A/C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73099610	TACAACCGAGTATTA[A/C/T]CCAGTCACAAATGCA	9873
rs185925219	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861560	TGTAACAAAACCAGA[A/C]AAGAATACTACAAGG	9873
rs185930775	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73128171	CTGACATACTTAATT[C/T]AAAAGGAATTGGGAA	9873
rs185931366	snp	A/C			missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72921940	TGATCATACACATTT[A/C]CATCAAGAGCCTGTA	9873
rs185937131	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73084439	TCTGTTGCCTAGGCT[C/T]GAGTGCGGCGGTGAG	9873
rs185937757	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941474	TAAAATATAGACTCC[C/T]AACTCTATTAATATA	9873
rs185938043	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987321	TCATTTATCATTAGG[C/T]AAAATTAACCTCTAT	9873
rs185939617	snp	A/C/T			intron-variant	FCHSD2	GRCh38.p7	11:72896277	AGGTAAAGGGGAAAG[A/C/T]GTATTCTCATTCCGA	9873
rs185960628	snp	A/T	0.00716266	0.059414	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842466	ACTGACTGACAAGTC[A/T]CTGGTTTCCCAAATG	9873
rs185964058	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72959206	TTTCTTTTCCACTTC[A/T]TATATCCAGCAGTCT	9873
rs185970980	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023956	TCTGGGAAAGACCAA[C/T]TGATAGAGAAAACAG	9873
rs185981405	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73027966	TGGAAACCTCTGCCT[A/G]GATTTCAGAGAATGT	9873
rs186002943	snp	A/C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72990747	ACTAAATGCCCACAA[A/C/G]AGAAAGCAGGAAAGA	9873
rs186118724	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981634	GTAAATGTGTTCTTT[A/G]AAACTGTTGGTCCTT	9873
rs186122986	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73064235	GATGTTCTTTGAAAC[C/G]AATGAGAACAAAGAC	9873
rs186126968	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009867	ATAGTTTGACTATAA[C/T]GTACCATGGAGAATG	9873
rs186133124	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72938451	GATAGTTAAGGGTGT[A/T]CAAAGCAGTAGCCGG	9873
rs186146076	snp	G/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73104183	ATTAGTGAGAAACAC[G/T]ATGTACACTGCAACT	9873
rs186160830	snp	C/G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73040943	CATGACAGCAACTTT[C/G/T]TTAGCTCCCACATAT	9873
rs186167142	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997670	AAAAATCCTGGAACT[C/G]AAAAGTACATTAAGA	9873
rs186173498	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73023409	TCATCAAAGAAGATA[C/T]AAGAATGGCAAACAA	9873
rs186186758	snp	A/C	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:73079316	ATTCTCCTGCCTCAG[A/C]CTCCTGAGTAGCTGG	9873
rs186190641	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099041	CCACATAGTAAGACA[C/T]CATCTCTACAAAATA	9873
rs186199066	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73059124	TACTTTCAGTGAGAA[C/T]GCACACTATAATTCA	9873
rs186204721	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014883	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	9873
rs186244449	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73082682	CCATGTAGAAAATTT[A/G]CTGTATGTTAATTTT	9873
rs186249879	snp	G/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73068907	GTAGTCCCAGCTACT[G/T]GGGAGGCTGAGGTAG	9873
rs186255263	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73046434	GAATACCAATTTTCA[C/T]AGAAAGGAAACAAAA	9873
rs186255333	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73055593	TTCATTAAGATTTTA[C/T]GCATATTTTATAATG	9873
rs186267882	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110166	TTTTTTTTTTTGATG[C/T]GTCTTTGGTCTTTGG	9873
rs186277858	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131981	AGTCACTGACATCCA[C/T]ATATTTCCACAAATT	9873
rs186283532	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73086479	TACAACTTAAGGAAC[C/T]AGAAAAAGAACAAAT	9873
rs186286239	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73083544	CAAAGCGAGACTCCA[C/T]CTCAGAAAAAAAGAA	9873
rs186314162	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860305	ACATTTATAGAACAT[A/G]ACCCCTAACAATAGC	9873
rs186315057	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855916	CTATTAGAATATGCA[C/T]GTTTTACTTTTTAAA	9873
rs186330048	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017834	TAAACAATCACAAAT[A/G]TATATAGGAAAATGT	9873
rs186333490	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875804	CTTTGGCTAGTGGGG[A/C]ATTTGCCAATTTAAT	9873
rs186336835	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73121004	TTGTTTAGACAAGAG[C/G]CAGAGAGCTACTAGT	9873
rs186337358	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72936922	GTAAGTCCAATGTAT[A/G]GACTTCCTTGGAGAC	9873
rs186340632	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72979606	GACTCCAATGTTTCA[A/G]TGAAAGAGTTTTCAA	9873
rs186341497	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139007	TCAGTCAGAAAACAA[C/T]AATCTTGATATATCC	9873
rs186347933	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72910946	CCATTCTGTGGGTTG[C/T]TGCTTCACTTTGTTG	9873
rs186376600	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72905041	TTTACAAACAGCTGT[A/C]GTGGGCTGAATGGTA	9873
rs186382560	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72918119	CCTTTAACTCCTTTG[C/G]TTAAGTTTATTCCTA	9873
rs186386691	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937533	ATATGGGACCATTAA[C/T]GGAAAGGCAAGGTCT	9873
rs186399419	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73127395	TCCATAAATTACTCC[C/T]GATCAACACTGACAG	9873
rs186425937	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035358	TTTTTTGTAGAGACG[A/G]GGGTCTCATCATGTT	9873
rs186465880	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73053858	ATTGTTTTCTTTTTC[C/T]CTATGTATGACCATT	9873
rs186467771	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72927432	TCATCAATTGCAACA[A/G]ATGTGCCACTCTGAT	9873
rs186468882	snp	A/G	0.00205798	0.0320118	intron-variant	FCHSD2	GRCh38.p7	11:72989100	ACTGGTCCACACACT[A/G]TAAAATACAAAAGTA	9873
rs186469440	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73032914	ACAGGAAATCAAGCT[C/T]GCGAGCAGTGCAGTG	9873
rs186477637	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932649	TCTCTTCACTTAATC[A/G]TCTACTTGGATATCT	9873
rs186485521	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088861	TTTCACAAAAGATAA[A/C]AGGAAATATTTAAAT	9873
rs186498849	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895911	ACAACGCTATATGCA[A/G]TACAAAATTTCTACA	9873
rs186507265	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72885246	ACCAAGTGAGATTAT[A/T]TTATGCTAACAGTAA	9873
rs186514264	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72860815	AGAGCAAGACTCTGT[C/T]TGAAAAAAAAAAAAA	9873
rs186520050	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73070381	TAGAACCTAGCATCA[C/T]GCCAGTCGTAAAGTA	9873
rs186525797	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73000851	TGAGAACATGTTGAA[A/G]TCAGAAAATCCTAGT	9873
rs186542221	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72891839	GTAGGTTATAATGAG[A/G]TCATATTTTAAACAT	9873
rs186543732	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118200	GGCAGGTGCATATAA[C/T]CCCAGCAACTTGGGA	9873
rs186547003	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73073748	GGCCATAATGCCATA[A/T]AAGTGGCTTTGAAGA	9873
rs186552347	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72957857	GTGAGGGAGAGGGAA[C/G]AAACAGAACAAAATG	9873
rs186553136	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998327	GGCAGATCACTTGAG[G/T]TCAGGAGTTCAGGAC	9873
rs186558808	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72854495	GGAGTGCAATGGTGC[A/G]ATCATAGCTCATTGC	9873
rs186563679	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72957019	TCAAAGGACTCTAGT[C/T]TTTTTTTTTTTTTCT	9873
rs186564718	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72874591	ATGCAAGTCATTTAA[C/T]TGCTGAAGCAGAAAA	9873
rs186608120	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73033304	AAAAAAAAAAAAAAG[A/T]AGTTAGACTACAGTC	9873
rs186623151	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112367	CTGCTGGACATATTG[A/G]AGCTCCATTATGTGT	9873
rs186625206	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73104909	AAATGGTGAAAATCT[A/G]TATTTTACAATATAG	9873
rs186632988	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036381	ATATTTCACAACGTT[A/G]TATCGGTCTTTGGAG	9873
rs186657825	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913162	TGATTTAATTACCTC[C/T]CACTGGCCCCTCCTC	9873
rs186665447	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72929538	TCAAAGCACGGGAAG[C/T]GGATGATAACCCTAT	9873
rs186678424	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949398	GAGGTTACAGTGAGC[C/T]GAGATCATGCCACTG	9873
rs186686917	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73036324	ATAGGAAATAAAAGA[A/C]AAAAAAAAAAAACCC	9873
rs186692169	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876859	TTATTATTATATATA[C/T]GTCCAGGATTTTAAT	9873
rs186694868	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72893504	GATTTTTAGTAGAGA[C/T]GAGATCTCACTATGT	9873
rs186698111	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878096	ATAAATAAATGTAAA[A/G]TCAAAGAAATCAAAT	9873
rs186712321	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72914592	AGACCGCACACCTAA[A/G]ACCACCTGATCTTCA	9873
rs186734312	snp	A/C/G	0.00057876	0.0170032	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840850	AAGAACTATGCATTC[A/C/G]ATAATCCTGCAAGAT	9873
rs186768935	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092453	CCCGGCATCTTCTAA[C/T]ATAGCATCTGCTTTA	9873
rs186775977	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143204	GAGGCCCCCGTTTCA[C/G]AGACGGGGAGGCAAG	9873
rs186781004	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72914857	AGATGCCAAAAGCAA[C/T]TGCAACAAAAGCAAA	9873
rs186791855	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72993868	CATATGTAACTAACC[C/T]GCACGTTGTGCACAT	9873
rs186792195	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72996151	ATAAACCTGTTTCAA[C/T]ATTAAGCTTTGTTTT	9873
rs186797187	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73134483	TCAAAAAAAAAAAGT[C/T]TCAGAACATCCATAA	9873
rs186800750	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72952623	AGCCACCATGCCTGG[C/T]CTATAGTTAATTTTG	9873
rs186802032	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72970347	TACTTACAATTCTAA[C/T]GTATGAAAATTGTCT	9873
rs186840540	snp	A/G	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:72965085	TGAGCCACCGCGCCT[A/G]GCCAATCATTTTACT	9873
rs186851236	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72847818	CTGCCTCAGCCTCCC[C/T]AGTAGCTGAGATTAC	9873
rs186853803	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055858	AGATTCAGGGGCTGT[A/G]GGAGGAGACAAAGGG	9873
rs186854312	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72850545	TTTTTAGTAGAGATG[C/G]GGTTTCACTGTGTTA	9873
rs186867395	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72885931	GAGGTGGGGTTACTG[A/G]GGTTTCTCCAGCCCA	9873
rs186890603	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140517	GCAGAGTGTGGATGG[A/G]GGCTGGGAGCCTAAG	9873
rs186891434	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73057991	TTCACGCCATCCTCC[C/T]GCCTCAGCTTCCCGA	9873
rs186904033	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039335	CCAGCCTAGACAAAA[C/T]GGTGAAATCCCATCT	9873
rs186918483	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73120398	TGTCTCATTTGGTAG[C/T]AAACATTTCTTCAGT	9873
rs186929867	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73076834	TGTTATGCTAGGCCC[A/G]GCGCAGTGCCTCACG	9873
rs186931990	snp	C/T	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:73097665	TCCCTTCACTTGTTA[C/T]TGAGAATTTCTATTT	9873
rs186942910	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72994387	CTCTATGAAAAAGGT[A/G]GTAGTAGTAGTAGCA	9873
rs186948625	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971871	TGGTGATTTGTTACA[C/T]AGCAACGGAAATCAA	9873
rs186953128	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73032109	GAAAAATGAATAGCA[C/T]GGTCCTATTTTAATT	9873
rs186999450	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014703	CCCTGGATTCTCTGC[C/T]ATTGTTTGAAGGGTA	9873
rs187001445	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72870328	TGATATAATTGGGGG[C/T]TCCTTTAAGACTCGA	9873
rs187002736	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72933527	TACTTTGAGTTGGGT[A/C]ATTGTTATTTGCAAT	9873
rs187003149	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839650	AGTAGGATGGGGGTT[C/G]CATTTACCAAGATAG	9873
rs187006338	snp	C/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72890060	CAAAACATGAGGCAC[C/G]CTCCACTACTGCTGG	9873
rs187014051	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72974809	AGAAAGAGGGCATTA[A/T]AAAAAAAAGGATATA	9873
rs187047564	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72869747	GTCTGTTTCCTTTTC[C/T]TGTTCATAATGCTAT	9873
rs187068617	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030197	CTTAGTTCCTATGTA[C/T]ATGTATGCGTGTGTG	9873
rs187070125	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051204	ATGGTGCTGCCAGTG[C/G]TGTTGCATGCTGAGG	9873
rs187071463	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73096500	AGGTTGCAGTGAGCC[A/G]AGATTGTGCTGCTGC	9873
rs187073173	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73123435	CAAATGAGAATCATA[C/T]GCTATGGCTTTTTAT	9873
rs187080392	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73011928	TCTTCTTAGTGGAGG[A/C]GGTACGAAGTGCCCC	9873
rs187084501	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085315	CAGCTTAGTAAACAC[C/G]AGGAATCTGACTCCC	9873
rs187092924	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73066513	TCTAATTAAACTAAA[A/G]AGCTTTTGCACAGCA	9873
rs187095780	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938603	CACAGCATCTCACCA[A/G]ATGGAGAAGCTTAGG	9873
rs187097506	snp	A/G	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73136198	GAAAAAAGAAGGGAC[A/G]TAATGGGGAAGAACT	9873
rs187097697	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73118984	CTAATAAATAAATAA[A/T]TAATTTTTGTTTGAA	9873
rs187118784	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72883220	AGAAAAGCTTGAACT[A/G]TAACACTTCTAGAAG	9873
rs187122703	snp	A/C	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72905924	GTGTCTTTATAGCAG[A/C]ATGATTTATAATCCT	9873
rs187127477	snp	A/T	0.02016	0.0983543	intron-variant	FCHSD2	GRCh38.p7	11:73052416	TATAATTTTTTTTTT[A/T]AAAAAAGACACCTGT	9873
rs187129479	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72919276	GGGCACTACATTATT[A/C]TTATTAAATTTTTAT	9873
rs187130587	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73053025	CTAATTTTTGTATTT[G/T]TAGTAAGATGGGGTT	9873
rs187137294	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848723	CAGAGGGAATGTTGA[A/G]TGAATGTGAACTGTT	9873
rs187143815	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72867778	ATTATCTTTTTAAAA[A/G]ATTTTGGCTATTATT	9873
rs187159861	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72949999	TGGCTGTTCCATTTT[A/T]CATTCTCACCCAATT	9873
rs187165736	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72986120	ATGAACACATATGCA[A/G]CCCAACTACTTCCCC	9873
rs187171619	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908371	TCTCTTTGATATATT[G/T]ATTTCCTTTCTTTTG	9873
rs187276589	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73088307	AGGTTTGTAGCCTAG[A/G]AGCAATAGGCTATAT	9873
rs187290288	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005567	ACTGGAGTGCCCTCA[A/T]GTCAGACCCCAGGCT	9873
rs187304287	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72870774	GCGTGGTGGCGGGTG[C/T]CTGTAGTCCCAGCTA	9873
rs187307526	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132272	TGGACTTCAATTTTC[A/C]ACTAATAACAGTAGC	9873
rs187308356	snp	C/T	0.0170251	0.090679	intron-variant	FCHSD2	GRCh38.p7	11:72851686	AGGCAGAGGTTGCAG[C/T]GAGCCGAGATTGTGC	9873
rs187331563	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73032577	AAATGTTTATTACCT[G/T]CCTAACTGAAAAAAA	9873
rs187348808	snp	A/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72866086	CTAGCTGAAGGAAAA[A/T]CATGGGTTTGATTGG	9873
rs187348829	snp	A/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72889321	TATTAATTCAACATA[A/T]GTCTCTTCCCCTGCC	9873
rs187349271	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73020672	TGATTATGTAAGATT[A/T]AAAAAACAGTATATT	9873
rs187360828	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72925685	TCCACCAGTAGACAC[A/G]ATTATCGAAATGGCT	9873
rs187361149	snp	G/T	0.00504829	0.0499866	intron-variant	FCHSD2	GRCh38.p7	11:72867845	AATCAACTTGTCATA[G/T]CCAAGAAAAGAAATC	9873
rs187367473	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002914	TCTCACTATAGTGAA[A/G]GCTCCATGAAGGCAG	9873
rs187370322	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72886656	ATAAAAGTGTGTGCA[C/T]AGGTCCTCCATAAAC	9873
rs187371368	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73047652	CAAATATTTATGCTC[C/T]TTCTTTCAGAAATGG	9873
rs187374852	snp	A/T	0.0629771	0.165899	intron-variant	FCHSD2	GRCh38.p7	11:72983305	TCTCAAAAAAAAAAA[A/T]AAATAAATAAAAGAA	9873
rs187376805	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72964980	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT	9873
rs187378103	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72922082	TGGACAAAAGATACA[A/G]ATTGTAAGTAAATAT	9873
rs187390428	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038651	AGCTAAACATTGAAT[A/G]CAAATGGACATAAAC	9873
rs187394491	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920510	CTTTGAGAGGCAAGG[C/T]GGGTGGACCACTTGA	9873
rs187398822	snp	A/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72939317	ATTGTAACTAAGCAT[A/T]TTTCCCCCAGTCGGT	9873
rs187401962	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72861396	TATTTAAAAACTTCC[A/C]AAAAAAAAAAAAAAC	9873
rs187414999	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72961896	ATTTCAACTCGATGT[A/G]TAAATGCCACATTTC	9873
rs187433664	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73008832	CTACTTAACATTTCA[A/G]ATATGAAGAGATCTA	9873
rs187456826	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73044710	TGGGTAAATACTATA[G/T]AGAAAACAGTGCACA	9873
rs187460323	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111641	ACTCCTGTTATTTTA[C/T]TTTTGGGTGTGTGGT	9873
rs187466666	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73069981	AAGACCAGGTAGAAA[C/G]TTAGAATGCACATAC	9873
rs187471323	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73090282	CCAGGCTGGAGTGCA[A/G]TGGCGGGATCTCGGC	9873
rs187481930	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73133624	GAGATGGCAAAACCC[C/T]ATCTCTACTAAAAAT	9873
rs187491604	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112744	ACCTCTGCCTCCCAA[A/G]TTCAAGCAATTCTCC	9873
rs187499384	snp	A/G	0.000121751	0.00780132	intron-variant	FCHSD2	GRCh38.p7	11:72900290	CAGAGCACTGACAGG[A/G]GAGAGCTCAATATCC	9873
rs187507922	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72975863	TATTAAGAATTACTA[A/G]GCTTTTAAAAAATCT	9873
rs187516175	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72923519	ATTAGTGATTAGGAA[C/T]GGTATATCTTTGTAG	9873
rs187517451	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72934601	GGCCTCCCAAAGTGC[C/T]GGGATCACAGGCATG	9873
rs187519009	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879955	CGTGAGCCGAGATCG[C/T]GCCATCGCATTCCAG	9873
rs187523959	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72900721	AGGTTGTAATATAGA[A/G]GGAAATGCTGATTTC	9873
rs187525312	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943801	TATTAGTTCATTAAC[A/T]ACAAGAAGTTTCAGT	9873
rs187526925	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72916041	TGGGAACAACGCACA[C/G]TAGGGCCTACCAGAG	9873
rs187551304	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72864170	GAAAGTGGCTGAAAA[C/T]GGGGAAGTGATGTTA	9873
rs187566279	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124554	AGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	9873
rs187574150	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081504	ATTTTGTATTAAAAA[A/T]TTTTAAAGCATATCA	9873
rs187577629	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946088	GCTGCTATAAAGACA[C/T]ATGCATACATATGTT	9873
rs187591670	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73021233	AGATCAAACATAGAA[A/T]AAAAAAAAAAAAAAA	9873
rs187609457	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72847148	ACGATAGGCATGTGC[C/T]ACCATGCTCAGCTAA	9873
rs187614168	snp	A/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72882120	ACTGCACTCCAGCCT[A/G]GGTGACAGCAAGACT	9873
rs187625691	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72856958	ACAAAAATCAAAACA[A/C]AACACAACACCCATA	9873
rs187625768	snp	C/T	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72918799	TTATTAATTGGAAGG[C/T]ATTTCCTTATGGAGA	9873
rs187642145	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024365	AGCTAGAAACTGTAC[A/G]ACTAAAGACAAAAAA	9873
rs187652822	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73007281	AATATCATATAAGAT[A/G]TCTAGGAAAACCTAG	9873
rs187656472	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882591	GTGATAGATATCTTA[A/G]TTACTCTAATTTGAT	9873
rs187660527	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72988033	AGCCCTTGATAAACC[A/G]CGGAGCCCCTGAATT	9873
rs187669352	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73061657	ATTGCTGAGGCTTGA[A/G]TAGGGTGGTTTTATG	9873
rs187682335	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72975066	AGAAAAACCGAAAAA[A/G]AACTTGGCTTTCTGT	9873
rs187682577	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042268	CAGGGGTCATTCTTC[C/T]GCATATGGATATTCA	9873
rs187683215	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106639	AGTAACATAACATTT[C/T]CATAAAAAATGGACC	9873
rs187693854	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953223	GAGAAAGCATGACAA[A/G]CATTAGAAACTAAGG	9873
rs187695250	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066052	GCATTGCCAAAACAA[A/T]CCTGGGCAAGAAGAA	9873
rs187708399	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062655	CATACACCGTTTCAA[C/T]AGCCAAATCGATCAA	9873
rs187714139	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72872868	TCTGGGGAAATACTA[A/G]ACTGTTTTTCAACGT	9873
rs187726818	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73026619	CTTAATTGAGAACTA[C/T]ATATGATTAAAGATC	9873
rs187728151	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915320	AAATTAGTTCAACCA[A/T]CGTGGAAGACAGGGT	9873
rs187733491	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72933883	GGAGGCTTAGGTGGG[C/T]GTATCACTTGAGCCC	9873
rs187734740	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72953412	ATAAATTCTCTCTCT[C/T]AAGGCCAGTTGAGAG	9873
rs187750074	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878501	CTTGGAGAAACAGCT[A/G]ATTCTAAGTCTGGGC	9873
rs187751465	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137015	CCTAGCCAACAGAGC[A/G]AGACTTTGTCTCAAA	9873
rs187752211	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852219	TTAAAAAGTCAAAAA[A/G]TAACAGATGCTGGTG	9873
rs187753457	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898881	ACTACAGGTGTGTGC[C/T]ACCATGCCCAGCTAG	9873
rs187761486	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72915779	GCCGAGATCACGCCA[C/T]TGCTCTCCAGCCTGG	9873
rs187774352	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029354	AAGATCGGTTTGATG[C/T]AATTATTTTAGAATT	9873
rs187823181	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102954	ACAACATGGATGAAT[A/C]TCAAAAACATTACAC	9873
rs187839590	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73133161	ACCCATCATGTATTA[C/T]TGCTGGTGGGAATAT	9873
rs187856959	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876609	TGGTCTTGTTGAATG[C/T]TCTATGTGTACTTTA	9873
rs187867615	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892585	TAGTATAGATAATTA[C/T]GTTTTTGTGTTTTTG	9873
rs187886663	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949476	AAGAAAAGAAAAGAA[A/G]GGAAAGAAAAAGAAA	9873
rs187886815	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72982772	TCTTTTGTTTGTCCC[A/G]TACGCAGCTCAAAAT	9873
rs187892739	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965554	TTTTTTTAAAACTCA[A/G]TATTTTCATGTATTT	9873
rs187896894	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856407	AAAACTGACTCTCCT[C/T]TTAACCACTGTTTGC	9873
rs187901758	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72905513	TTACACAGGTATACA[C/T]GTGCCATGCTGGTTT	9873
rs187904527	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141417	TAGAAACAAATCCCC[A/C]GCAAATTTGCAAACG	9873
rs187911426	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019742	TTACAGTAAAGGTCC[C/T]AAATAATATTGCACA	9873
rs187913161	snp	A/C	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72913812	TGATATACAAAAAAA[A/C]CAAAAAAAACCCAAA	9873
rs187938207	snp	G/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72867166	GAGAGTAATGGGTGG[G/T]GAGGTGACAGTAGGA	9873
rs187943531	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062116	TTCAGAGGAAAGATC[A/G]GCAGCAATCTTTGAT	9873
rs187960053	snp	A/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73043345	ATTATCAGTTTCCAT[A/T]AGCAAGTATTTATCA	9873
rs187971549	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967774	TATGGTATGTGAATT[A/C]TATCTAATTTTTTTT	9873
rs187975062	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124139	GCTGGAAACCATCAC[A/T]CTGAGCAAACTATTG	9873
rs187986293	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73084860	GACAATTTACCTTGA[A/C]TATCCTGAGTTTAAA	9873
rs187986695	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081154	TTAAAACTTTAAATC[A/G]ACCAGGCACTGTGGC	9873
rs187990704	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73102179	TAAAATGAGATACCA[C/T]TGAACACCCACTAGA	9873
rs187999986	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73129979	TGCCTCCCGGGTTCA[C/T]GTCATTCTCCTGCCT	9873
rs188003127	snp	A/G	0.0329836	0.124112	intron-variant	FCHSD2	GRCh38.p7	11:72909334	AGTCTCGCTCACTCA[A/G]TGCTCAATGTTGCCC	9873
rs188005617	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73129742	CCCCTGACCCCACCC[A/G]CAGTCCATGGGAAAA	9873
rs188013226	snp	A/T	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:72924553	TCCCAAAGTGCTGGG[A/T]TTACAGACATGAGCC	9873
rs188019894	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011687	TATCTTAGTTTCAAG[G/T]CCCAGGAAGGTTGAA	9873
rs188033301	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72873278	AGGCTGCAGTGAACC[A/G]AGATCGCGCCACTGC	9873
rs188035366	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72853500	ACTCACTGCAACCTC[C/T]GCCTGCCAGGTTCAA	9873
rs188041954	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73048516	ATGAATCTGCAGGTT[A/G]GCTAGAGCATCTCTG	9873
rs188051439	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72846423	CTGACCTCGCGATTC[A/G]CCCGCCTTGGCCCCG	9873
rs188053410	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72888931	CCAGCCAAACATATA[C/T]TTTCATGAAATCTAT	9873
rs188053870	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73056859	AGGCCAAGGTGGGTG[C/G]ATCACAGGGTCAGGA	9873
rs188084098	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72863288	AAGGACAGTTAAAAA[A/C]AAAAGTTCAAAAAAG	9873
rs188115229	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017364	AGAAATCATTAACAT[G/T]GAGATACTTATTTCT	9873
rs188165197	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869264	AAAAAAGGAAATCAA[A/G]GCTTTTTTCCCTCAA	9873
rs188194080	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73038500	TGGTACATATACAGC[A/G]TGGATACTATGCAGC	9873
rs188194861	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850249	TTTGTATTTTTAGTA[A/G]AGATGGGGTTTCACC	9873
rs188201864	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72960649	GCCATTCCCATTCCT[C/T]TAAAGTTACAAAGAT	9873
rs188209915	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73002748	CTTCCAGTCTCAGTT[G/T]AAATGTAACTTCCTT	9873
rs188210123	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72929987	TGTAAGAGGGAAAGC[A/G]CCAAAGAAACATTTT	9873
rs188211141	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075247	GAAAACCATTTCATG[A/G]TATTTCCTAAAGCTG	9873
rs188214918	snp	C/T	0.201418	0.245234	intron-variant	FCHSD2	GRCh38.p7	11:72962601	TGAACTAAATTCCCC[C/T]TTTTTTTTTTAAACT	9873
rs188242564	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055132	CTTATAAAAACCATC[A/C]GATCTCGAAAGAACT	9873
rs188244083	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071764	GAAATGGACAGAGTG[A/C]AACACAGGTTTCTTG	9873
rs188253689	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73010576	GATAGATCTATGGTG[C/T]TGTTTGGTAGGGCCC	9873
rs188262611	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034536	ATAGAGATCAAAGTT[G/T]CCACTCTTGTGAAAA	9873
rs188263615	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928059	AAGGTAAAGGATGTG[A/G]TATAATGTTAGTCTT	9873
rs188263941	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72906683	TTTATTAAACTGAAT[C/T]CTTTCCCCATTTCTT	9873
rs188264695	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73115518	TCTATACTTTCGTGT[C/T]GTTTTCATGTCTTCT	9873
rs188273904	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969457	ACTGAGAGGGACAGA[A/G]ACAAAAAGATGAATC	9873
rs188275736	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73134200	TCAGCACCATGCACA[A/G]TGGCTCATGCCTGTA	9873
rs188282848	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73091694	AGCAAATGTGGTCTT[C/T]TCCACTTGGAATTTC	9873
rs188317584	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73074606	AAAAGAAAAAAAATA[C/T]ATTTCCTTAAAATTA	9873
rs188329649	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73120051	AGGAAGATGCAAAAG[C/T]AGAAACCCCTGATAA	9873
rs188349089	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73107451	TAATAATCACATTAG[A/C]GTAAATGGGGTATCC	9873
rs188359255	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73082386	AAAGCATTCAACAGA[A/C]ATATTAAAACTGATG	9873
rs188375631	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72843813	AACACAGCGAGACCC[C/T]CATCTCTACCAATAA	9873
rs188386442	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879084	CCACTGCACTCAAGC[C/T]TGTGCGACAGAGTGA	9873
rs188389203	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73012865	AAAACTCTGCCAAAT[C/G]ATTTGCAAGTCCTCT	9873
rs188403376	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994836	ATCTTAAAAGCTTTT[A/G/T]AAAAATTGACATATA	9873
rs188410484	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72888131	AAACAAGATAGCCAA[G/T]TATAGGAATCTGAGA	9873
rs188436826	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931728	AGAGATCGCACCACT[A/G]CATTCTAGTCTGGGT	9873
rs188443012	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72951857	GAGGAAATGAGGCTA[A/G]CGTTCAGTATAGCAG	9873
rs188446950	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72851966	ATTGCAGTGTCAACC[C/T]CCTGGGCTCAAGCAA	9873
rs188452241	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72907348	CTTGCCTGATTGCCT[C/T]AGCCAGAACTTCCAA	9873
rs188457629	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73021374	ATGGAATACTATGCA[A/G]CCATAAAAAACAATG	9873
rs188459369	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72973439	TATATACAATGAAAT[A/G]CTATATAGCAAAGAT	9873
rs188460456	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921484	TAGTACTCTTTGTAC[C/T]GACACATGACCTGTT	9873
rs188461678	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72895635	CAGATCAGGAGAAAG[A/G]TGACTAAACCAGTAG	9873
rs188464790	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72941062	ATTGGTGGTTCTTGC[C/T]GGGCAGCTTAGAGAA	9873
rs188474062	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72869503	AAGAAAGGAATCAGG[G/T]TCTCCTAACAATGGA	9873
rs188478537	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914315	TCAGGTGCCCAGCCT[G/T]CCCTAAGCAATTTAT	9873
rs188481358	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73070749	AAATTAAAAAAAAAA[A/G]AGAAATTGAACAAGT	9873
rs188485147	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73028919	AGTTTCCTGAAGGCT[C/T]CCAAGCCACGTGAAA	9873
rs188497795	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73099924	CCCGTCCCTATCCCC[C/T]ACTAATGAGGCCTTT	9873
rs188507295	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057539	GACAGAAGGGAAGAA[A/G]AGAGGAAGGGAGGGA	9873
rs188512724	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850400	ATTTTATTTTTGAGA[C/T]GGAGTCTCGCTCTGT	9873
rs188535705	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117834	ACCTTATTTTTGGTG[A/T]CTTTAAAGCAAATTG	9873
rs188542700	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72911610	TATTTATTCTCCCAA[G/T]CCATCAACATGGAAT	9873
rs188548999	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72883825	TATTCCCAGCTACTC[A/G]GGAGGCTGACATGGG	9873
rs188552561	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033063	GGGGGCTGAGGCATG[C/T]GGATCATGAGGTCAG	9873
rs188552972	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72992298	ACATTCCATGCTCAT[G/T]GGTAGAAAGAATCAA	9873
rs188555206	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72948619	TTAACAAAATTTTAA[C/T]TTACCATTTTAATGG	9873
rs188561646	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954630	TTGTCATTACTGAAA[C/T]TGGGAAGATCAAAAG	9873
rs188562410	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73134324	AAAAATACAAAATTA[A/G]CCAGGCATGGTGGTG	9873
rs188576890	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998895	AATGATGCAGCTGCT[A/T]TGCAAAACAATTCTG	9873
rs188595798	snp	A/G	0.000988419	0.0222088	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843416	ACTCCTAAAAATGTC[A/G]CAAGAAAGGGCGATA	9873
rs188616081	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963347	CTATCTCATTTAGAT[G/T]TCCTAAAGCAATCTG	9873
rs188626890	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73136256	TACAGTCTAATGTGC[C/T]GTAGATTTTTTTTTA	9873
rs188627175	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096657	AAAAGGTGCATCCTT[A/G]TGTTCTTCCTGAACT	9873
rs188686890	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73068465	CACAAAATTTACCTA[C/T]GTAACAAACCTGCAC	9873
rs188692282	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72872226	TTTTTTTGGTAAAAC[G/T]TTATTGACATATAGC	9873
rs188697008	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052261	CAATAAACATGATTT[C/G]AGTTTAAATTTTGTG	9873
rs188697362	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73031803	AGGTAAGAGCTGGCA[C/T]AGCAGCCTTTTCGCC	9873
rs188702916	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109311	CTGTAGATTGCTATA[A/G/T]AAACTATGGACATTT	9873
rs188706353	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72908950	TGAGCCATTGCATGT[G/T]GCCCTGTCTGCTATT	9873
rs188707078	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73138130	GAGCAACAGACTATA[C/T]CAACTTAGCTTAGAT	9873
rs188710779	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131674	GCACCACTGCACTCC[C/G]GTCTAGGCAACAAAC	9873
rs188717949	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944159	TCCTCAATAAAATAC[C/T]GGCAAACTGAATCGA	9873
rs188718115	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72988107	AAACTGTATTAGAAA[C/G]ATAGCCCCCTCCTTA	9873
rs188719078	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086416	CCATCTCAAAACAAA[C/T]AAACAAACAAAAAAC	9873
rs188746994	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909174	GCTGAGTGTCTGGGA[C/T]TGCAGGCACACGCCG	9873
rs188753750	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73013191	TCCACCACTCCAGTT[A/T]ACCTCTAACCCACAT	9873
rs188769907	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73005205	CAGCTGCCACCCTAA[C/T]GTCTGCTCTCTTTTA	9873
rs188773854	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054135	ATTGTCTATGGCTGC[C/T]TACACTCTACAACAG	9873
rs188776247	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72985569	GAAAGACTCTAACAA[C/T]AGGCTCTATGAAGTC	9873
rs188786416	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72964705	CTTTATGGTAATAGC[C/T]TTACTGGTATTCTTG	9873
rs188789967	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73090857	TTGTACAACCACCAC[C/T]ACCTCTAATTTCAAA	9873
rs188792690	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942163	TCCTCACAGTAATGA[C/G]AGCGTTCTCACTCTA	9873
rs188813535	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72977622	TATGTGCTGCCGAAG[C/T]GAGCACGCTCTCACA	9873
rs188833365	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935709	TGAATTTATCAGTTG[A/G]TATAAAGTAAAATCA	9873
rs188839453	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080832	ACCTGTAATCCCAGC[A/T]ACTCAGGAAGCTGAG	9873
rs188847554	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025155	ACATACCCAAAGGAA[C/T]ATAAATCATTCTATT	9873
rs188849741	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73016290	CCTGGGTGACAGAGT[A/G]AGGCTCTGTCTCAAA	9873
rs188871989	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73010924	ACAGCAGTGGCAGTG[A/G]TGGGATAATCTTCTG	9873
rs188894363	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72868801	CTATCAGTCTTACAT[A/G]GCAAATATTCTCAAG	9873
rs188900965	snp	A/C/G	0.00279242	0.0372774	intron-variant	FCHSD2	GRCh38.p7	11:73040894	CAAACTGCTCCCCCC[A/C/G]CTCTTTGGTAACTAT	9873
rs188902893	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023204	AAATTGGACCTTATC[A/G]GAATTAAACTCTTTC	9873
rs188908941	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73066828	CATTAAAAAGTCAGG[A/G]AACAACAGATGCTGG	9873
rs188925524	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108376	TTCACTTTGTTGATT[A/G]TTTCCTTTGCTGTAC	9873
rs188929739	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058936	CAACCAGAAATATAA[C/T]TGCATATGAGTTTCC	9873
rs188934820	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894623	TATTTATCCTCAAAA[C/G]GACTTCTTCAAGTAA	9873
rs188935888	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130529	ACCTGCCTTGGGCTG[C/T]AATGGCTGTCCCATT	9873
rs188936640	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72914216	GATGGGGTTTCACCA[C/T]GTTGGCCAGACTGAT	9873
rs188956217	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966469	CCGGACTAAACTGAG[C/T]ATATTACTTTGTTAT	9873
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	9873
rs188964925	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877215	TAATGATTAGTGTTT[A/G]TTCTCCTGTGATAAG	9873
rs188969663	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72859594	AAGGTTCGGTACTAT[C/T]TGTGACTTCAGGCAT	9873
rs188987844	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72924299	TTTCTTTTTTTTGAG[A/T]CAGAGTCTTGCTCTA	9873
rs188989972	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73007500	TGGTGGTAGTGGTGG[C/T]TATGCAGGAGGTGAT	9873
rs189020991	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978618	GTGACTGGATTATAG[A/G]AGCGATTTCCCTGAT	9873
rs189021683	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72888596	AGAGTTTAGTCTTCG[A/C]GATATATTTTCTTTC	9873
rs189030245	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72865596	CCTTCACAACGAGAA[C/T]AGCCCTTCTTCTTTA	9873
rs189031415	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863015	GTAACCTTGAACTTC[C/T]GGGTTCAAGATACCT	9873
rs189035949	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73044863	ATCACGAGGTCAGGA[A/G]ATCGAGACCATCCTG	9873
rs189046555	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72903508	ACAGGCGTGAGCTAC[C/T]GCGCCCGGCCTGGAA	9873
rs189050305	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027293	GAACTTATTGAGAAC[C/T]AGAGCAAAGGTCACT	9873
rs189054347	snp	G/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73009217	AATCATACTACAGGC[G/T]GGGTGTGGTGGCTCA	9873
rs189060222	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958343	GCCAATGTGGTGAAA[C/T]TCTGTCTCTATCAAA	9873
rs189072826	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73063187	CATATCCAGCCTAAC[C/T]AAGCTTCATAAGCAA	9873
rs189075039	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73127157	TATACTCCAACTTGT[G/T]TCTGTGGAACCACAG	9873
rs189078294	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73113705	GTTTTCCAGGCATTT[A/G]AAGAAACACCCATTT	9873
rs189081339	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73082119	GAGGTAGGCGGATCA[C/G]GTGGTCAAGAGATTG	9873
rs189097888	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72844690	AAGCTTTCCCCAAGT[C/T]CCAAGATGGGTTAAA	9873
rs189115800	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989671	ATACACATATACATT[C/T]GAGGAGAAGGGATGG	9873
rs189123668	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:72967959	AGCCGGGTATGGTGG[C/T]GGGCACCTGTAGTCC	9873
rs189160479	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73082716	TTCTAACAATCTCCC[A/G]TATTTTAAAATTTTT	9873
rs189176430	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72849217	ATGTATTCACGCCTC[C/T]CTTCCAACATTCATG	9873
rs189186394	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860515	AAATTCAGTAACACA[C/T]TTTTAATTACCCATC	9873
rs189192090	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72884442	AGTAACAGGCCCAGA[A/G]GTAATATAAATTTGG	9873
rs189210868	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838038	TCAGATCCGGAAGTT[A/C]CATTTCTGCTTTAGC	9873
rs189226497	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139269	GATGAGGCTTACAGA[C/G]CCAATTCCAATTTGA	9873
rs189275882	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73031116	GTGAAATAAGCCAGA[C/T]AGAAAGAAGACGACT	9873
rs189283796	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72917048	GGAGTGCAGTGGTAC[A/G]ATCTCAGCTCACTGC	9873
rs189293763	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73000571	TAGTCAAAATGTGTT[A/C]ATTTCCTTTAAATTA	9873
rs189302338	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72956466	CTGATACAAGAAATA[C/T]CATAAACTGTGACTT	9873
rs189302446	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067453	CTGCGCGTTCTGCAC[A/T]TGTATCCCAGAACTT	9873
rs189315874	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72881635	AGATGTGGAATCAAC[C/G]TAAGTGTCCATCAGT	9873
rs189325569	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73082323	GCCTGGATCACAGAG[C/T]GAGACTTGTCCCAAA	9873
rs189325945	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72962417	AAAGCTCTTTGATTC[C/T]TCAATAATTTTTAAG	9873
rs189346026	snp	A/C	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73063854	TGGGAGACTTTAACA[A/C]CCCACTGTCAATATT	9873
rs189351914	snp	G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72920934	AGAGCTCTGGTACAG[G/T]GAAAACAAGAATATA	9873
rs189361588	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73103861	AAAAGTCCCATGAAC[A/C]AAGCAAACTCTCCTC	9873
rs189370237	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126641	GTTATGCTTAACAGA[C/T]ATGCAATAAAATGTT	9873
rs189370769	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72889516	GGAGTTTGAGACCAG[C/T]CTGGGAAACATGGCA	9873
rs189373071	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73104220	ATTAAATAGCACATA[C/T]AGTATCATTTACTTT	9873
rs189376734	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935993	GTGGGCTAAAACCAC[A/G]TAATATTTAGGTTGC	9873
rs189383138	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955294	TACTTACTCATTTAT[C/T]ATAAAACATTATTAC	9873
rs189393181	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978261	ACATGTATACATATG[C/T]AACAAACCTGCACAT	9873
rs189396762	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72854715	AAAATACTCTGATTC[C/T]ACTTATTTGAGGTAT	9873
rs189406604	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72875218	AATAATGGTAGATAA[C/T]AGTATTTGCTACTCC	9873
rs189410587	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72903103	CCAAATAGTGTTTGT[A/G]GAGTATTTCTCAGCA	9873
rs189416999	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916528	CTATGTTGCCTAGGC[A/T]GCTCTTGAACTCCTC	9873
rs189438652	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73072860	CTTCTTGTATAGTAT[A/G]CCCAAGTCTTCATAA	9873
rs189462062	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840332	AAAGCTAATAGGGGT[C/T]AAGGAAAATAAAATT	9873
rs189480763	snp	G/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72906982	GTGGTAGCTTGATGG[G/T]GACAGCATTGAATCC	9873
rs189526697	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73016936	GATTTTAAACTGCTC[A/G]TTCCAATTATACAAT	9873
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	9873
rs189532103	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72999374	ACCCAGGCTGGAGGG[C/T]AGTGGCACGATCTCA	9873
rs189546279	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72876889	TATATTCATGATGAA[A/C]TGTCTTTAAAAAATC	9873
rs189558195	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73033275	CCTGGGCAACAGAGC[A/G]AGATTCCGACTCAAA	9873
rs189573466	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73098610	ATAGTCCAGGAAAAA[A/G]AAAACAAACATCTAT	9873
rs189590133	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086157	TCACGCCTGTAATCC[C/T]AGCACTTTTGAGAGA	9873
rs189604263	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73051668	TGCAGAGATGTACTG[A/G]CTATGCAACAATAAA	9873
rs189624868	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73096278	GGGAACAGTGGCTCA[C/T]GTCTGTAATCCCAGC	9873
rs189631801	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056693	GAGAGCATAACAGAA[C/T]AATAAGTCATATGAC	9873
rs189634855	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72877899	TAGCCCCAGCTATTC[A/G]GGAAATGGAGGTGGG	9873
rs189637821	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73074518	AATTCCAGAACATTG[C/T]ATAACACACCTCAAG	9873
rs189643707	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72985136	AATAAAAATAGAAAA[G/T]TATGTTTAATAAAAT	9873
rs189644324	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939836	GTTTGTCAGGCTGGT[C/G]TTGAACTCCTGACCT	9873
rs189648566	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72984322	TCCCCAACAAGAATA[A/G]AGGTAACCACGTGCG	9873
rs189651189	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72926890	GAATGTCAGCCAGAA[C/T]TATACAGATGTGCAT	9873
rs189657617	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118716	ATGATGATACTATAA[A/T]GATGATGGCAAACAC	9873
rs189661661	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72947546	AGTCACTGAGTCTAG[A/C]AAGAAATGGGTATAT	9873
rs189666268	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135848	TCCTCCCCTCGAAAT[C/T]CCAAAAGATAAGAAC	9873
rs189678401	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72848551	ATATTTAACCCTTCA[C/T]AGATTGTCCATTCCT	9873
rs189681274	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022467	GCTCTCCTACATACA[C/T]GCAATGAACAACTGG	9873
rs189683307	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72968878	ATAGTAACATTAAAA[G/T]ATATTTCTATAAATT	9873
rs189683434	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72875520	TTTTTTGTAGAGATG[A/G]GGTCTTGCTATGCTG	9873
rs189685855	snp	A/C/G			intron-variant	FCHSD2	GRCh38.p7	11:72890659	AAGGTACTATGGAAA[A/C/G]TGCTTCATATAACTT	9873
rs189690609	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910735	AGAGACCTTTGTTCA[C/T]GTGTTTATCTGCTGA	9873
rs189691958	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73037648	TTAGGGCCCATACTG[A/G]TTATGTTATGAATGT	9873
rs189699139	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72867402	TATGTGAGGAGAATA[C/T]GAAAGCTGTCAAGAA	9873
rs189719184	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73092150	CTTCTTTTTTAGAGG[A/T]AGGGTCTTGCTCCAT	9873
rs189775324	snp	A/C	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72893778	CTCTAGTCCCTTTAG[A/C]ATAAAATATTACAAT	9873
rs189800067	snp	A/G	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:72858155	GGTAATACCTAATAC[A/G]GAGGAAGACAGCTCC	9873
rs189800427	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72972278	ACCATGTTTTGATTT[A/G]TATTTTTATGAGTTT	9873
rs189814170	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009954	TAAATCTCGTTAGAC[C/T]TGGGAAGTTTTTGTC	9873
rs189815053	snp	A/C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953278	GATCTCCAGAAACCT[A/C/G]CTGCTGGTGATGAGT	9873
rs189818767	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908273	ACATTTTCTCTATCC[A/G]TTCATCTGTTGATGG	9873
rs189822186	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990917	AAAAATCAATGAATC[C/T]AGGAGCTGGTTTTTT	9873
rs189840762	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040964	TCCCACATATCAGTG[A/C]GTGAGAACATGTGAT	9873
rs189840977	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72997723	TGTTTTGTTTTGAGA[A/T]AGGGTCTCCCTCTGT	9873
rs189844708	snp	C/T	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72915446	AAAGACATATGCCTG[C/T]TTATGTTCATTGCAG	9873
rs189850804	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72975073	CCGAAAAAGAACTTG[A/G]CTTTCTGTTCCTGGC	9873
rs189853247	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933930	CTTGGGCAACACAGC[A/G]AGACTCCATCTCTAC	9873
rs189855355	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120661	TTCATCTTGGAAGGC[A/G]GAGGCTGCAGTGAGC	9873
rs189859425	snp	C/T	0.000903138	0.021231	intron-variant	FCHSD2	GRCh38.p7	11:73077653	GGATAAACTGTGGTA[C/T]ATCCATACAATGGAA	9873
rs189863288	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72930690	GGAGGCTACAGTAAG[C/T]CAAAATCGTGCCACT	9873
rs189898793	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73003872	AGCACTCTGGGAGGC[A/C]AAGGTGGGCAGACTG	9873
rs189899316	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73038369	AAAAAAAAAGGAAAA[A/G]AAATTCTGATGACTG	9873
rs189903723	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73120797	AAGACAGTCTTGCTC[C/T]GAAAAAGCTCACAGT	9873
rs189910850	snp	C/G/T			intron-variant	FCHSD2	GRCh38.p7	11:72871605	CAAGTTGGAGCTGGT[C/G/T]CAGTGGCTTGTACCT	9873
rs189930079	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73136204	AGAAGGGACGTAATG[A/G]GGAAGAACTAGACAA	9873
rs189939143	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040448	TCTGGTGTATATTTC[C/T]CAAACACCATACAGT	9873
rs189953401	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73051268	TACGGTGAGCCAAGA[C/T]TGCATTATTGCACTT	9873
rs189982556	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73078998	TGTTGGGATTACAGG[C/T]GTGCGCTACCGCACC	9873
rs189990903	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72854434	CTGTCTGTCTACCTA[C/T]CTGTCTATCTGGTTA	9873
rs190000462	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72887080	TAAGCTCTGAAAATA[C/T]ATATATATATATGAA	9873
rs190026566	snp	A/G	0.0130921	0.0798413	intron-variant	FCHSD2	GRCh38.p7	11:72851527	GGGCGGATCACAAGG[A/G]CAGGAGATCGAGATC	9873
rs190046133	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72870744	TCTCTACTAAAAATA[C/T]AAAAAATTAGCTGGG	9873
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	9873
rs190068660	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73024507	TGGCAGAGGGTAAAA[C/G]CTCAGTGTTGGAGTG	9873
rs190075895	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950516	ATATATGCTGTGAGG[C/T]AGAGGTCCAACTTCA	9873
rs190076755	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72934135	AAAAAAAAAAAAAAA[A/G]AGCTATTTAAAGCTT	9873
rs190079731	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73030868	GCAAAAAATCCTGAA[A/T]ACAATATTATTAACT	9873
rs190081817	snp	A/G	0.0016993	0.0290992	intron-variant	FCHSD2	GRCh38.p7	11:72921955	CCATCAAGAGCCTGT[A/G]ATAGAGGAGTAAATA	9873
rs190090868	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72994658	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	9873
rs190096243	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73001303	AAGCAACATGGCATA[C/T]ACTCTATTCTTCTTA	9873
rs190097592	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73065157	CAAAAAGCTTATCCA[C/T]CATGATCAAATCAGC	9873
rs190116108	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028763	TGGATCATGAGGGCA[G/T]ATTTTCCTCATGCTG	9873
rs190118694	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73103033	ATCTACTGTATGATT[C/T]CATTTATATGAAATT	9873
rs190129213	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73035443	CGAAGTGCTGGGATT[A/G]CAGGCATGAGCCACT	9873
rs190139090	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73083672	AAGTATACCTAGAAT[A/G]GGACCTCCAATTTCA	9873
rs190143877	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73138753	GCTAGGACTACAGGC[A/G]CACGCCACCATGCCT	9873
rs190145498	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105588	TTACATCTACAAAAT[A/G]TACTTACTAGGCAGT	9873
rs190163953	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72871963	CAATTTATGTTCTGA[A/C]TTGTATCACTGGGCT	9873
rs190180922	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72925587	CATTCAAGAAGGAAT[C/T]TGTTGCCACGGTGTA	9873
rs190220177	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098825	TAAAGGAAAACACAG[G/T]GGCAATTCTTCATGA	9873
rs190254836	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73108745	GGCTAATTTTTTTTT[A/G]TATTTTTAGTAGAGA	9873
rs190261433	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72874359	GCCTGGCTAATTTTT[A/T]AAAATTTTTTGTAGA	9873
rs190267731	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72987457	AGGCCTTAAATTCCT[C/T]GAGGGCACAAAGCTT	9873
rs190286665	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72885237	TAAGTGGAAACCAAG[A/T]GAGATTATTTTATGC	9873
rs190293960	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73112553	GTTTGGGAAGTTCTC[C/T]GTTGTTATCCCCGTG	9873
rs190301716	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72910296	CGCCTTTGTCCGGCC[A/G]CCCCGTCTGGGAGGT	9873
rs190302225	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73133245	CATAGAGTTACCATA[C/T]GACCCAGACATTCCA	9873
rs190302628	snp	A/C	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72943678	TTAAAATATAAAATT[A/C]TATTGGCTGTTTTGT	9873
rs190306157	snp	A/T	0.0217236	0.101931	intron-variant	FCHSD2	GRCh38.p7	11:72915146	AATCATATGAAAAAA[A/T]CTCAACATCACTGAT	9873
rs190311907	snp	A/G	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:72880687	TTGGGAGGCTGAGGC[A/G]GGTGGATCCCTTGAG	9873
rs190317672	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933623	TCTTTTGGTTGCATT[A/G/T]TAAGGAAAAAAAGTT	9873
rs190328057	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72965151	CTGTAGAACAATTCT[G/T]AACAGTGGATACAAC	9873
rs190330340	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72887985	GAAAAGAAGATGTCA[A/C]AACAGGCAAGAGATT	9873
rs190332287	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72995590	GCACCTGTAGTCCCA[A/C]CTACTTGGGAGGCTG	9873
rs190332454	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72908885	TCTCTAACTCCTGGG[A/C]TCAAGCGATCTGCCC	9873
rs190337763	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861644	TCAATATATAGAAAG[A/G]ATAGGCCGGGCGCGC	9873
rs190340712	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923070	TGGTGCCTGGCTTCT[C/G]TTGCCCAGCATAATA	9873
rs190346058	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72878221	GAGTTCAAGGCTATA[C/G]TACACTATGATTGTG	9873
rs190350193	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896401	CCATCCCAGCTTCGC[G/T]TTGTCCTTTTTCACA	9873
rs190354399	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980384	CTGCTTAGATACAGA[C/T]TATCCAGTTATGGGG	9873
rs190357383	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72845086	TGTGACAGCAAACCA[C/G]GGAGGTAGTACACTT	9873
rs190364265	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055616	TTATAATGTATACAA[C/T]ATATTAGTACAGAGT	9873
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	9873
rs190383163	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017906	AGTATAATAGCTATT[A/C]TTTCTATATTTATTA	9873
rs190387640	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945781	ATTTATGCAGCCAAA[C/T]GATACATGAAAAAAT	9873
rs190421568	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909530	GCCCCTCTGCCCGGC[C/T]GCCCTGTCTGGGAAG	9873
rs190438558	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72990069	GAAAGGACTACAGGG[A/G]ATGAGACATCTAGAA	9873
rs190471915	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027588	AGAAAAACCAATTTT[C/G]TGAAGAGAAATTCAA	9873
rs190483440	snp	A/C	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73054957	GCTAAATAAAGACAT[A/C]CTTGAGACTGGGTAG	9873
rs190490512	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131046	TTTTAAATACCTGAG[C/T]CCAGTACCTGATCTG	9873
rs190518528	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846706	ACCAGAGCTCCGTTT[C/T]CACCAGTATCTCTCC	9873
rs190541369	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73110351	GGCGATATTTTATTA[C/T]GGCTTCAATCCTGTT	9873
rs190546070	snp	C/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73081124	TTAAATAATAAACAT[C/G]TCCTATTTACTTGAT	9873
rs190548890	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72856157	ATGTAGAAAACTACG[C/T]TAGCCTCTTTGATGG	9873
rs190552398	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73042355	CACCTTTGTCAAAAA[C/T]CAGTTGGCAGTAAAA	9873
rs190559953	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72926165	GTTCCCAGTAAGGCC[C/T]CACCTTCAGGCCAGG	9873
rs190575648	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131995	ATATATTTCCACAAA[C/T]TACCATCCTCCATGC	9873
rs190581085	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73100959	TCTCCTCACACAGAC[C/T]CTTGTTTTTTACCAA	9873
rs190596897	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72905602	TAGCCCCCCACCCCC[C/T]GACAGGTCCCAGTGC	9873
rs190600427	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73014124	AAATCTGTGTGGTTT[C/T]TTTTTTTTTTTTTTT	9873
rs190601612	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72864427	GCATGAGCCTGTAGT[C/T]CCAGCTACTCAGGAG	9873
rs190616605	snp	C/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73024657	GGATCTAATTAAACT[C/G]AAGAGCTTCTGCACA	9873
rs190618626	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73007460	ACCTCATCTCTACAA[A/G]AAAAATTTTAAAATT	9873
rs190633612	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72988044	AACCGCGGAGCCCCT[A/G]AATTTTCACAAGTTG	9873
rs190655223	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72917345	TTTCTGAAGAGAATA[A/T]TCTTTCTCTATTGAA	9873
rs190665296	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72937356	TTTAAATAGTCTCTT[C/T]TGTGTGCATTTTTGA	9873
rs190673415	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72865759	GTGGGGGTGGGGAGT[C/G]GGAATCTCAGAGTCT	9873
rs190688332	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72881745	AATATAAATGGAACT[A/G]GAGGTCATTATGTTA	9873
rs190695859	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72968503	GATTCCAATACATAG[C/G]ATCAGAATAACTGTG	9873
rs190714429	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071462	CTTGAGAGGTCGAGG[C/T]GGGCAGATCACGAGG	9873
rs190716684	snp	C/T	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73045974	TTGCTTATATTTCTA[C/T]AATAATTTCAGTAAT	9873
rs190717521	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72982005	TATATACTAAAACAC[C/T]TAAACCTCTAGGTCT	9873
rs190726646	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009367	CCAGGTGTGGTGGCG[C/T]ACACCTGTAATCCCA	9873
rs190756842	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73099333	GTGAAGAAATTAGAA[C/T]CCTCATGCATTGCTG	9873
rs190758003	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72938511	CCTTGCTGGTGTCTA[G/T]GTGTGCCCACAGCCA	9873
rs190758987	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73059754	CCCTAGCTGTGAACA[A/C]TTCCAGAATTCTGGC	9873
rs190762991	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032709	AAGGCTTCCCCAAAG[G/T]AAATGAAAATTGACA	9873
rs190769348	snp	C/G	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:73014886	TCTCACTCTGTCGCC[C/G]AGGCTGGAGTGCAGT	9873
rs190770993	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73010349	TTTCTTGTATCTCAT[C/T]GAGCTTCTTTAATAT	9873
rs190774583	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73019234	AAAGCAGAATGACAG[C/T]ACTCTAAATTTATGT	9873
rs190778787	snp	G/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:72991610	GCTGGTTCAACATAC[G/T]CAAATCAATAAACAT	9873
rs190780372	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046563	AGAAATATAAATTGG[C/T]GTAGCATTTTAAATT	9873
rs190789717	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121840	TCAGAGTTCCTGATG[A/C]AGGAGATTAGGGATA	9873
rs190852823	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72919231	ACATGGCATAAAACT[C/T]GTAGGCCTCTTCTGG	9873
rs190880695	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72883061	AATGGGAAAAGCATA[A/C]TCTTTAAAATATGAT	9873
rs190899543	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056361	ACAGGAGTTATTTTT[C/T]ACTGCTAGGGAATAC	9873
rs190899721	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73036386	TCACAACGTTATATC[A/G]GTCTTTGGAGTCAAA	9873
rs190907527	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72899434	GCAAACCAGAACCAC[A/G]AGATACTATTTCATA	9873
rs190911109	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72855401	GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC	9873
rs190914713	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73018549	AATCATTATATCCCC[A/G]GCTATAGCAGATCAC	9873
rs190923921	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005600	TTCTCTTCTCTAACT[A/G]CATTCACTCTGTTGA	9873
rs190944507	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72959036	GTGTGTACATCCATG[A/C]GTGCATGGGACACAC	9873
rs190948531	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72922374	TTATACATTGGTATA[G/T]GTATATTTACTGAAC	9873
rs190950850	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928604	CTCAACTAGCTCTTC[C/T]TTAGCGTTTTCACAA	9873
rs190965840	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73001946	ATGCCTTAGTCAATT[A/C]TAGCATGCTCCTACA	9873
rs190974896	snp	A/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72980957	GGGCATTATCACCTT[A/T]ACATTAATTCAGAAA	9873
rs190984914	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73028188	GTACCTGGAAAAGCC[A/G]CAGGCACTCAATGGC	9873
rs190984973	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72998133	AGACATGAACAGAGT[A/C]AAAAGGTCTAACAGC	9873
rs190986362	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937795	ATACAGGGTGCTAGA[A/G]GAGAGGCACCTAGAC	9873
rs191003486	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119660	CACTGTGTTGCCCAG[C/G]TTGGTCTCACTCCTG	9873
rs191010171	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73064456	CAGAACTGAAGGAGA[C/T]AGAAACAAGAAAAAC	9873
rs191014379	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72960114	ACTGTACAAAAAGCA[C/T]AGTGCCAGGATCTAT	9873
rs191015771	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72999315	ATCTTACCAAAGATT[C/T]TTTTTTTTTTTTTTT	9873
rs191029087	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73002161	GTGGTCAACAGATGA[C/T]AGTGTAGAAGCAAGA	9873
rs191057746	snp	G/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73075046	GCCCAATCAAGATAT[G/T]AAAAGTTCCTCTAAT	9873
rs191091455	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878141	CCCTCTGGCTGGGCA[C/T]AGTGGCATGCAGTTG	9873
rs191098015	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72851700	GTGAGCCGAGATTGT[A/G]CCACTGCACTCCGGC	9873
rs191133172	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986668	CCCAAATAGGCTGAG[C/T]TGCATGTAGATCTTC	9873
rs191155895	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943095	CTCCCGGGTTCAAGT[A/G]ATTCTCCTTCCTTGG	9873
rs191161055	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73023460	CATCACTTGTCATTA[C/T]GGAAATGCAAACTAA	9873
rs191183511	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72908585	AGCCACCTGAACTAG[C/G]ATGATATAATATCTT	9873
rs191184885	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73106417	TCTCCAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA	9873
rs191189848	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878852	TGGCTCATGCTTGTA[A/G]TCCCAGCACTTTGGG	9873
rs191191035	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024111	CAAAGAACTTTGACA[A/G]TACCCACAGAACTTT	9873
rs191195099	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73129025	TACAGGCATGTGCCA[C/T]CGTGCCTGGCTAATT	9873
rs191197672	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73029810	AGAGAAATTAGTAAG[A/T]CACCACAATATACAG	9873
rs191203349	snp	A/T	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:73011727	CATGGCCAGCACTAC[A/T]GAAGTCTACAGTGGG	9873
rs191203925	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73084635	TGGCCTCAAAGCAAT[C/T]CTCCTGCCTTGGCCT	9873
rs191230535	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73061285	GAACAGATACTGTGC[A/T]TGTCGCATGGTTTTC	9873
rs191233090	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949399	AGGTTACAGTGAGCC[A/G]AGATCATGCCACTGC	9873
rs191237251	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72892908	CGTGCGTGGCTGGTA[A/T]TTTTTTTTTTAAGAC	9873
rs191241979	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096517	GATTGTGCTGCTGCA[C/T]TCCAGCCTGGGTGGC	9873
rs191262507	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72914760	AAAGACTTAAATGTA[A/C]AACCCGAAACTATAA	9873
rs191265796	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994193	ATGCTAGATGCTTCC[C/T]TACTGGCAAATTGTG	9873
rs191267726	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72913453	TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCGCC	9873
rs191272653	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72971693	TGAATGACCCTGGAA[A/G]GAGATTCTTCCCCAG	9873
rs191274601	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72929548	GGAAGTGGATGATAA[C/G]CCTATGATTTGCTCC	9873
rs191276265	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72952575	AGTGATCTACCGGCC[C/T]CGGCCTCTCAAAGTG	9873
rs191276485	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907195	TTTTGTATCCTGAGA[C/G]TTTGCTGAAGTTGCT	9873
rs191306923	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73127647	CTCCTCAGATAAACA[C/G]CTTCAGACTTGATAC	9873
rs191321953	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73057078	ACAGAGCAAGACTCC[A/G]ACTCAAAAACTAAAA	9873
rs191338603	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72896207	ACATCAGAAATTTAG[G/T]GTCAGCTTTTTGCTG	9873
rs191346354	snp	C/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73099686	AGGCTTAGCGGCGCT[C/T]ACCACCCTGGTTCTT	9873
rs191350191	snp	A/G			missense, utr-variant-5-prime, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73140034	CTATAGCCTTACCTC[A/G]TATCTTCAAGCAAAT	9873
rs191351993	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73058273	GCATTAACACTTGAG[G/T]TTATTACAGCACAGA	9873
rs191366525	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861078	TCAAGAAAATAGAAA[A/G]GAGAAAAACGAGGGA	9873
rs191384737	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72909194	GGCACACGCCGCCAC[A/G]CCTGACTGGTTTTTG	9873
rs191408308	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72873087	ATAATCCCAGCACTT[C/T]GGGAGGCTGAGGCGG	9873
rs191420783	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72888693	GCATGATCTTACCTC[A/G]ATGTAACCTCCACCT	9873
rs191432676	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73006819	CACTGTTGTATGTTC[A/G]GCACAGGGTATGGCA	9873
rs191446100	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852772	ATGACAAGTTGAATA[A/C]AGAAAATGTGGTACA	9873
rs191451802	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72869875	GACCTCATCATGTTG[C/T]TCCCCAGTTTAAAAA	9873
rs191465767	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73042209	GGACTACAGGCATGC[A/G]CCACTGCACCCGGCT	9873
rs191478698	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085785	AAATCTGGTATTCTG[G/T]TTCAAGTTGATGTTT	9873
rs191483241	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73120589	ACAAAATTAGCCGGG[C/G]GTGGTGGTGCATGCC	9873
rs191488916	snp	A/G	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:73107935	GGATATATACCCAGC[A/G]CTGTGATTGATGGAT	9873
rs191494064	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73077094	CAGCCTGAGACTCTG[C/T]CTCAAAAAAAAAAAA	9873
rs191499485	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73097970	ATAGCCCATGGTGCC[C/T]AGCTCTTCTTCTAAT	9873
rs191500216	snp	A/C	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:73086978	AAATATTGTATGATT[A/C]CAATTATATGAGGTC	9873
rs191500976	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066557	TCAGAGTGAACAGGC[A/C]ACCTACAGAATGGGA	9873
rs191503604	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932786	CAGGTCTGTCTGTTT[A/G]CCATTCCATCTTCTG	9873
rs191509868	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137098	TCATTCCACTTACTA[A/G]GGCAGACAAGAGAAG	9873
rs191521488	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974423	AAAAGTCCCACTTCT[C/T]AGTATTGTTGCATTG	9873
rs191522557	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73130091	ATGTTAGCCAGGATG[A/G]TCTCAATCTCCTGAT	9873
rs191533302	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73014715	TGCTATTGTTTGAAG[A/G]GTATTTGGTCATAAT	9873
rs191540603	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73036336	AGACAAAAAAAAAAA[A/C]CCCAAGCTTCATAAT	9873
rs191547534	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72974840	AAGCAAGAGAAGCAG[A/G]GATTTAACAGAATTA	9873
rs191560483	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051213	CCAGTGGTGTTGCAT[A/G]CTGAGGAGGGAAAAT	9873
rs191562122	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030408	TGAATATACAAAACT[C/T]AATTTACCATACATA	9873
rs191573725	snp	C/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73011934	TAGTGGAGGAGGTAC[C/G]AAGTGCCCCTAGTCA	9873
rs191597009	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73122344	AAGAAACATCAAGAC[A/G]TAGACTCTGCTGCAG	9873
rs191650364	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72952678	TAAGAGCTTATTGGT[A/T]GAGATGAGACATTAA	9873
rs191692914	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72969243	CGGAGCTGCATTCCA[A/G]TGTTTATTATCTTCA	9873
rs191693431	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72850722	ATATTTATCAGTATC[C/T]TTTCACTTTTCACTG	9873
rs191705546	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886166	TTGGGTCCCTGAAAG[A/C]TGCTTGCCCAGAATC	9873
rs191708354	snp	G/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72909408	ACCTCCCAGCTGCCT[G/T]CCTTGGCCTCCAAAA	9873
rs191710517	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008964	ATATAAATAAGCTTA[A/C]TTAAAAGTCATTAGA	9873
rs191718941	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72989225	TCAGTACGTTCAGTG[C/T]CCTTCAAATTGCAGA	9873
rs191719006	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73032919	AAATCAAGCTTGCGA[A/G]CAGTGCAGTGCCATT	9873
rs191721065	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73015420	ATATTTAGAATTTAT[G/T]TCAAAAGTATCAGTG	9873
rs191721309	snp	A/T	0.0329836	0.124112	intron-variant	FCHSD2	GRCh38.p7	11:72924696	TTTTTTTTTTTTTTT[A/T]AAATACACAAATTCT	9873
rs191723184	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927796	GGCAGAGAAGCCTAC[C/T]ATCCTGAATAGGGTC	9873
rs191726173	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72967789	ATATCTAATTTTTTT[A/T]AAAAAGAAGTGGGCA	9873
rs191732342	snp	C/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72944935	AACATTCCATGCTCA[C/G]GGGTAGGAAGAATCA	9873
rs191753097	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73069085	GGAAGCCAAGGTGGG[C/T]TAATCACCTGAGGTC	9873
rs191753262	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72891942	AATTACTTGAAACAA[A/C]AATTTTCTTATTACT	9873
rs191756586	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889065	GTTCATGCCATTCTC[C/T]TGCCTCAACCTCCCG	9873
rs191775254	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855955	CTAATAAAGAAGAGA[C/G]AAACAGCCTCAAATA	9873
rs191800010	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72996232	CCCACTCTGTTATTT[A/C]CTACCTAAGTCTCTT	9873
rs191829901	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032162	ACTCTAGAATACATA[C/T]GAACTTGGAAATGAG	9873
rs191841276	snp	A/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73088936	AATAAGGACATTCAC[A/G]TGAAGTCCACAAGAA	9873
rs191851035	snp	C/T			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72843922	CTGAGGTGGGAGGAT[C/T]GCTTGAGCCTGGGAG	9873
rs191853918	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73053881	TGACCATTTAAATTA[C/T]AGATTGAAATGTAAC	9873
rs191855649	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73070394	CACGCCAGTCGTAAA[A/G]TAGATACTTGATAAA	9873
rs191857841	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72863534	AAAAATTTGTGCTCT[C/T]TGAAAGGTATTAAGG	9873
rs191868874	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73111684	CTTTCCTTCCTTCCT[A/G]TCTTCCTTTTAGTGA	9873
rs191872423	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73070093	GTAAAAAAGGAAACT[A/T]ATCAGTAACAAGAAT	9873
rs191888101	snp	A/C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72847417	ACTAATGACCTACTA[A/C/T]GTGCTGGGCATTGTC	9873
rs191903064	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882124	CACTCCAGCCTGGGT[A/G]ACAGCAAGACTCCGT	9873
rs191940194	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140545	AAGAGTGCCTGATAC[C/T]CAATGACCAATATTT	9873
rs191959813	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72844828	ATCAATTTCCCATTT[C/T]ATGAACATTAAAACA	9873
rs191974030	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72992394	CAATGACTTTCTTCA[C/T]AGAATTGGAAAAGAC	9873
rs191979902	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72864221	AAAATGTAAGCAATA[A/G]AAGAACAGGGTGGGC	9873
rs191989417	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73093046	GAGGCTGGAGGCTAA[A/G]GCCAGCCGCATGAGT	9873
rs191991072	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73065396	CAAACCCACAGCCAA[C/T]ATCATACTGAATGGG	9873
rs192004615	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029092	CCAGAAAGGGCACCA[C/T]AAATATAATGGTGTA	9873
rs192020347	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72948851	TTTATATTTTTAGTA[C/G]AGATGGGGTTTCACC	9873
rs192022594	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72948250	TGGACTCAAGCAATC[C/T]ACCCACCTCAGCCTC	9873
rs192032705	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72918412	TGTCTAGGACTTCCA[A/G]TACAATGGTTAATAG	9873
rs192046403	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72876065	TGGCTGACACCTGTG[A/G]TCCCCACATTTTGGA	9873
rs192058290	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911046	GCCTGTGCTTGCAGG[A/G]TATTACTCAATCTTT	9873
rs192090261	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73135144	CAGGCATAAGCCACC[A/G]CACCCAGCCTCCTGA	9873
rs192105075	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73132959	AAATGGGCAAAGTAC[C/T]TGAATAGACATTTCT	9873
rs192110798	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965720	ATTCTATGTACACCC[C/T]TCACCCAAGATAACC	9873
rs192112753	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72935822	AGGAAACAAATAAGG[A/G]AGTTTATGTCTGTAA	9873
rs192120707	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72954682	AAATCAAAGGCTGAG[C/T]AGGTAACCAGGCTGG	9873
rs192137030	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880500	ACATTGGGGAAAGGA[C/T]ACCCTCTTCAATAAA	9873
rs192139113	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900778	AGAGCTACTTAAAGT[A/G]TAAGAAAAGTAATGA	9873
rs192149361	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73133725	ATGAACCCAGGAGGC[A/G]GAGGTTACAACGAGC	9873
rs192149530	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73082128	GGATCACGTGGTCAA[A/G]AGATTGAGACCATCC	9873
rs192154379	snp	A/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72916232	ATTAAAGGGAAAAAA[A/T]GGTTTATCAATTTTG	9873
rs192157021	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876860	TATTATTATATATAC[G/T]TCCAGGATTTTAATA	9873
rs192158918	snp	G/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73103160	GTTCTATATATTGAG[G/T]GTAGTAGTGTTTAGT	9873
rs192162330	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088500	GTACTAAAATAGTAA[G/T]GAAAGTTTTCTCTGG	9873
rs192191951	snp	G/T	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:72866276	GTTTTGTTTTGTTTT[G/T]TTTGTTTTTTGAGAC	9873
rs192192296	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125419	ATTAAGAATGCATGG[C/T]GTAGATCGAGTGTGG	9873
rs192234537	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73050258	GTTTGCCAGCCTCTA[C/T]ATTAAAAAGAGGGCT	9873
rs192236942	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72984336	AAAGGTAACCACGTG[A/C]GGAAAACATTTATAC	9873
rs192263780	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085137	TTTCAAAATAACAAA[C/T]GGAAGAAGTTTCACC	9873
rs192263892	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73021727	AACTTAAAAAAAAAG[C/T]TCATTCATGACAGAA	9873
rs192265166	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938986	CATTTAATAAAAGTG[A/G]CCTCTGAGCTACTAA	9873
rs192274627	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961030	CCTAGGAATGGGGAG[C/G]TAACACACATGTGAG	9873
rs192281172	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72940195	CTTTTAAACTCATCA[C/T]TACTGAGATTCTAAA	9873
rs192286311	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883506	AATACTTTACTAAGG[G/T]GGATATATGAAGGGC	9873
rs192286560	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72982825	TTACCCATAAATTCA[C/G]GATAAACGTAATGAA	9873
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	9873
rs192292988	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010670	AGTGTCAGTGGTGTT[C/T]GTAATTTATTCAGTG	9873
rs192298962	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72906052	TAATTTACACTCCCA[C/T]CAACAGTGTAAAAGT	9873
rs192305686	snp	A/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72919472	AGAGAATATAGTAGA[A/T]GATCATGGAAAGCAC	9873
rs192309940	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72848919	TTTTCAAAAGATTAT[A/C]AAAACGATTTACATT	9873
rs192313668	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72969773	CAGCAAACTCCACAC[C/T]ATGTTATTTGTGATA	9873
rs192322684	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047883	ATCTCATTTAAGCTT[A/G]GCAACAACTGTGAGT	9873
rs192329800	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118210	TATAATCCCAGCAAC[A/T]TGGGAGGCTGAGGCA	9873
rs192342195	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73073986	AACTGATTCTAAAAT[G/T]TATAAGAAAATATAA	9873
rs192348382	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102569	CTCCTCTAAAACTCA[C/T]GTTGAAGTTTAATTG	9873
rs192353971	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73124202	ACTCATGGATGGGAA[C/T]TGAACAATGAGAACA	9873
rs192356667	snp	G/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73071555	AAAAAAAAAAAATTA[G/T]CTGGGCATGGTGGTG	9873
rs192358457	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73081159	ACTTTAAATCGACCA[A/G]GCACTGTGGCTCATG	9873
rs192368433	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055001	GTTTAATGGACTGTG[A/G]TTCCACGTGGCTGGG	9873
rs192368532	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73033499	ACTCTGACCCCTCAC[A/G]TTTTAGATCTACTAG	9873
rs192372894	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72905358	CAGGACTACAATGTG[C/T]AATAATCATATCAAG	9873
rs192385240	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72846094	GATAGATAGATAGAT[A/T]AGTAGTTACGATTAC	9873
rs192385945	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129809	GGTTGGGGACCACTG[C/G]TGTAAACTAGCACTT	9873
rs192398642	snp	A/C			intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842881	CTGGTAAGATAATTA[A/C]CAGCCGGTTGCTTTT	9873
rs192426140	snp	C/T	0.0267878	0.112589	intron-variant	FCHSD2	GRCh38.p7	11:72924503	TAGCCAGGATGGTCT[C/T]GATCTCCTGATCTCG	9873
rs192428711	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73017099	ACAATCCTCCCAACT[C/T]AGCCTCCCAAGTACC	9873
rs192430829	snp	C/G/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72999444	CCTGTCTCAGCCTCC[C/G/T]GAGTAGCTGGAACTA	9873
rs192439617	snp	C/T	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:72978292	TGTGCACATGTACCC[C/T]AGAACTTAAAGTATA	9873
rs192472611	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72863026	CTTCTGGGTTCAAGA[C/T]ACCTTCTTGCTTTAG	9873
rs192523772	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962155	GGACCACTGGGGGGA[A/G]TCTCTGAGACCCTTT	9873
rs192537114	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72893646	TCTTTTAAAAATGTA[C/T]TTGATACAAAAATTA	9873
rs192538959	snp	C/T	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:73021074	GTAGAGATGGGGTCT[C/T]GCTATGTTGCCCAGG	9873
rs192550766	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002925	TGAAAGCTCCATGAA[A/G]GCAGGGGTGTATGTC	9873
rs192556299	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72912224	CTTGTCATGTTCCAA[A/G]TCTTAGAGGAAACGC	9873
rs192556824	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983595	AATAGAAATATTCTT[C/T]TGCATAAAACTTTTC	9873
rs192575341	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73038576	CTGGCAACGATTATC[C/T]TAAGCAAACTAACAC	9873
rs192581474	snp	C/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72876757	TCAATTACTGAAAGA[C/G]GGATCCTAAAGACTC	9873
rs192582257	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971969	TTATGATAGTGACAA[C/T]ATGGTTATACATATT	9873
rs192585468	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73002857	AGCACTTTTCTTTTA[A/G]TTATAAATATTTTAA	9873
rs192587919	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856488	TCCCATAAATATGTA[C/T]AAATATTATGTGTCA	9873
rs192603746	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72892850	ACCTCGTGATCCACC[A/C]GCCTCGGCCTCCCAA	9873
rs192605891	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73130648	AGGTATTACCAAAAC[C/T]CTAATTCTTTCAATT	9873
rs192624511	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108533	TAGCAGTTTCATAGA[C/T]TGAGATTTTAGATTT	9873
rs192639454	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73003728	CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC	9873
rs192644353	snp	A/C	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73057918	AGAGTCTCGCTCTGT[A/C]GCCCAGGCTGGAGTG	9873
rs192658767	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076413	TAAGAACCTCAAAAA[C/T]ATCTGCTAAGCGAAA	9873
rs192663545	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106875	ATTCTATGATGTTGA[C/T]ACAAGGATGAAATTA	9873
rs192667505	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039906	TTAAATTTTCATATC[C/T]CTAATTAATATTCAT	9873
rs192670225	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038670	ATGGACATAAACATG[A/G]GAATAATAAACACTA	9873
rs192670960	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73066239	CCTGACACAAACAAG[C/T]AATGGGGAAAAGATT	9873
rs192685910	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921255	ACTGCAAAACATTTT[A/C]ATCTATCAAATCTTG	9873
rs192702404	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72962680	GATTTCCTATCAAAT[C/T]CTGGAAAAGATGGTT	9873
rs192707079	snp	C/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72998674	GGATTTAAAAAGTAA[C/G]AAGCTAATAGTGGAG	9873
rs192727732	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953526	ATTTCAACCACATGA[A/C]TTTATTGAACATGAA	9873
rs192736109	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72853829	GTTATGTATCTTAAA[A/G]GGGACTAATATCCAG	9873
rs192739088	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915832	CAAAAACAAAAAACA[A/C]AAAGAAAAGAAAAGA	9873
rs192752692	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72879319	CAAAACAAAACTCAA[C/T]AGTCTTTATAAGAAG	9873
rs192756400	snp	A/T	0.00636936	0.0560724	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143982	CAAGGGGACAGGTGG[A/T]TGGAGGCCCAGGGCC	9873
rs192787151	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73026903	CTTGCTTTCCCTTTG[C/T]CTTCTACCATGATTT	9873
rs192793408	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73102980	TACACTAAAAAAGCA[A/T]ATTACACTATTAAGT	9873
rs192794725	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843644	TGATTTTGAGAAACA[A/T]GTTGAACATAAAAAT	9873
rs192800451	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73062668	AATAGCCAAATCGAT[A/C]AAGAGGAAGAAAGGA	9873
rs192808587	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72872275	TTGGCACACAACTTT[A/T]TTTTTCTTTTCTTTT	9873
rs192816074	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909020	CCCCATTTTTAAATC[A/G]AATTATTAAATTTTT	9873
rs192839956	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994591	ACTCACGGTGAAACC[A/C]CGTCTCTACTAAAAA	9873
rs192844531	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73019770	ACATTTCTGAAAGCA[C/T]TCTATGCTTAAATTA	9873
rs192853753	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72949792	TGATGGACATTTGGG[A/T]TGTTTCCACCTTTGG	9873
rs192858401	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016313	GTCTCAAAAAAAAAA[A/C]AAAACAAAACCCAAT	9873
rs192871727	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73090375	GGACTACAGACGCCC[A/G]CCACTACGCCCAGCT	9873
rs192872573	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73054180	TTGACAGAGACCATA[C/T]GGCCCTCAAAGCATA	9873
rs192892249	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72977771	GATTCCTCAAGGATC[C/T]AGAACTAGAAATACC	9873
rs192897489	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943828	CAGTTAGCACATCTA[C/T]AATTAAATATTTGTT	9873
rs192938520	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72900452	AAGATTTAGGGCTGC[A/G]GTTGGGCTGGGAAAA	9873
rs192947505	snp	G/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72873679	GACTTACCCCTGTGG[G/T]TTTTTTTGTAAGTTT	9873
rs192948695	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934636	GCTGTGCTTGGCCAT[A/G]AATTTCTTAATCAAT	9873
rs192954128	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72893872	CATTCCAATATTCTT[C/G]ATATATTAGTCTTTA	9873
rs192962601	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930037	AGGCATTTATCTTAA[C/T]TGGGTCACCTTTATT	9873
rs192966461	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72967623	GGAGTAGGGAGAACA[A/C]AAAATGACAGCCAAT	9873
rs192967860	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72858534	AGAAGACCAAATACC[A/G]CAAATTCTCATTTGT	9873
rs192969098	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73124578	CTGGCCAACATGGTG[A/G]AACCCCGCCTCTACT	9873
rs192991765	snp	A/G	0.00835973	0.0641091	intron-variant	FCHSD2	GRCh38.p7	11:73044831	ATCCCAGTACTTTGG[A/G]AGGCCGAGGCAGGTG	9873
rs193011273	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73081931	TTCAAGATCGGGCGC[A/G]GTGACTCACGCCTGT	9873
rs193015275	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72888370	CACAGACATCATTGG[C/T]GATTTTGGTAAGCTT	9873
rs193026056	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73016503	CTTTTAACTATTTGA[C/T]TAGCCATAAAAACAA	9873
rs193026093	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73114840	CTCCTCTTCTCAAGC[A/G]GAAGGAGGGGGTCTT	9873
rs193028483	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73007710	GAAGAGGTCACACAA[A/G]GCTACAAATGTGGTA	9873
rs193030796	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72852001	CCTGCCTCAGCCTCC[C/T]AAATAGATGGGACTA	9873
rs193038651	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966545	GCCTGCATAGCTTCA[C/T]TGCAAGCTCCCTGCA	9873
rs193048075	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73044459	GTGGCACACACCTAT[A/T]GTCCTAGCTACTCAG	9873
rs193061979	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73033245	GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC	9873
rs193069365	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72998906	TGCTATGCAAAACAA[C/T]TCTGGTCATTTGGGA	9873
rs193074617	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73070752	TTAAAAAAAAAAAAG[A/C]AATTGAACAAGTTAT	9873
rs193104091	snp	A/C	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72920678	TTTTCCCCCAACATT[A/C]TTTTCTGAAAAATTC	9873
rs193113592	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883886	GCAGTGAGTTGAGAT[C/T]GTGCCACTGCACTCC	9873
rs193124741	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72849502	TAAGAAGGAACTATT[C/T]GAGCTGAGCTTCAAT	9873
rs193128718	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72923635	CCTACTCAAGTCCTT[A/C]ACTCATTTTTAAATT	9873
rs193138368	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030920	ATATCTCTATACTTG[C/T]GCGTCCTGAATTTCT	9873
rs193150069	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73136392	TGGTAAGACCCCATG[A/T]CTACAAAAAACACAA	9873
rs193150356	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73097185	TTTTTGTATTTTTTC[A/G]TAGAGATGGGGTTTC	9873
rs193151549	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73066922	TTGTGGAAGACAGTG[C/T]AGCGATTCCTCAAGG	9873
rs193171980	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112962	TGAGCCACTGCCCTC[A/G]GCCAGATATGCCCTT	9873
rs193181761	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913925	TGCTCAAATAAATTA[C/G]AGATGATACAAACAA	9873
rs193183004	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72898738	TTTCTATTTTTTTTT[A/T]TTTTTTTTAAAGACA	9873
rs193212315	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134118	AAAAAAAAACTCTAG[A/C]CCAGATTAGATTACC	9873
rs193214932	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73090959	TGTCAACTACTAATC[C/T]AATTTTTTGTCTCTA	9873
rs193219671	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72988237	AGCTCTCCTTCTCAC[A/G]GATGTCTTCAGAGTC	9873
rs193225680	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73062548	GAACCTTGAAAAAAC[A/G]TTAGACGAATTGCTA	9873
rs193227612	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73025283	GAAAATGTGGTATAT[A/G]TATACCATGGAGTAC	9873
rs193262030	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939383	CTTTCTAAGGAATGG[C/T]TTTTAAATTATTAAA	9873
rs193267770	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869067	GTGTACCACCACACC[C/T]GGCTAATTTTTGTAT	9873
rs193269410	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72906827	TTTTGGTTACTGTAG[C/T]CTTGTAGTATAGTTT	9873
rs193297324	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120282	GAAGATTACATATTA[C/G/T]AATGTAGCATATGGT	9873
rs193299512	snp	C/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73085973	TACTAAACAAAGATA[C/G]TAAAACAATGGTTTT	9873
rs193300514	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73051323	CTAGCTCTAAAAAAT[A/G]AAAAAATAAAAAATT	9873
rs199509377	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73111834	TTTTAAACTGATGAC[-/A]AACACTGATTGCATA	9873
rs199515499	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72907496	AACTCTTATTATTTT[C/G]AGATATGTTCCAACA	9873
rs199515890	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72956825	ATGATTTCATAGTGG[A/G]AAAAAAAAAAAAACC	9873
rs199517517	in-del	-/AGGAGG	0.0359534	0.129167	cds-indel, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73141927	GCGTTAGCAAGGACC[-/AGGAGG]AGGAGGAGGGCCGGA	9873
rs199528205	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73011057	TTGTAGTGGCAGGGG[A/C]GGGTAGAACCAACCT	9873
rs199534784	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72950637	ACAATCAGCTACTGA[C/T]GTATGATTAGTAGTC	9873
rs199550363	in-del	-/TATTTATTTATA			intron-variant	FCHSD2	GRCh38.p7	11:72903196	AGGAATTTATTTATT[-/TATTTATTTATA]TATTTATTTATTTAT	9873
rs199550489	snp	A/C			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143612	TTTTTTTTTTTTTTT[A/C]AGTCACGGGGCTGTG	9873
rs199617683	in-del	-/A	0.0295035	0.117819	intron-variant	FCHSD2	GRCh38.p7	11:73049434	TGAACTAAATAAACT[-/A]ACAAATTTTTATGAT	9873
rs199617864	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73039930	TATTCATGAGGATAT[A/G]ACAAAAGCAGTTATA	9873
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	9873
rs199623642	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73116952	TTTCCATTTTTCCCC[A/C]AAAAAAATCACTATT	9873
rs199632936	in-del	-/AATAT	0.0228947	0.104514	intron-variant	FCHSD2	GRCh38.p7	11:73033990	AATAGAAATCATGAA[-/AATAT]AATAGACAATTTTAA	9873
rs199660269	snp	C/T	0.000711385	0.0188464	intron-variant	FCHSD2	GRCh38.p7	11:72984258	AGTGCAAACTGATAT[C/T]GTACTGCAAAACACA	9873
rs199682597	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72866257	CAACTCTGTTCTGTT[C/T]TTTGTTTTGTTTTGT	9873
rs199698613	in-del	-/AAAT	0.0528381	0.153711	intron-variant	FCHSD2	GRCh38.p7	11:72846046	TATTGAAGGGATTAC[-/AAAT]AAATAGATAGATAGA	9873
rs199723808	snp	C/T	5.7468e-05	0.0053601	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73000999	CAATACCCTTTTTAG[C/T]TGCTGTTCTTTTAAG	9873
rs199757942	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72864608	TGTTTGTCAATTAAA[A/T]AATAAATAAATAAGA	9873
rs199788957	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72957020	CAAAGGACTCTAGTC[-/TT]TTTTTTTTTTTCTTC	9873
rs199797068	in-del	-/TTA			intron-variant	FCHSD2	GRCh38.p7	11:73097382	GTTTATTTTATTTAT[-/TTA]TTTTTTTTTTTTGCA	9873
rs199797090	in-del	-/TTTG	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72866268	TGTTTTTTGTTTTGT[-/TTTG]TTTTTTTTGTTTTTT	9873
rs199841948	in-del	-/T	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:73073833	GTACATGTGCAAGGA[-/T]TTTTTTTTTCTTTTT	9873
rs199843128	in-del	-/A	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72916123	GGTACTAGGCTTAAT[-/A]ACGTGGGTGATAAAA	9873
rs199857250	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73082637	CATTATTTATAATGA[A/G]AATAAAAACAGTAGC	9873
rs199859279	in-del	-/TATAATA/TATAATATA/TATAATATACTGAATGCT/TATAATATACTGAATGCTT			intron-variant	FCHSD2	GRCh38.p7	11:72907441	TGCTTCCAGTTTTTG[lengthTooLong]CCCATTCAGTATAAT	9873
rs199874957	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73069019	CCATCTCCAAAAAAC[-/A]AAAAAAAAAGGCCAG	9873
rs199878479	in-del	-/GA			intron-variant	FCHSD2	GRCh38.p7	11:72956824	GATGATTTCATAGTG[-/GA]AAAAAAAAAAAAACC	9873
rs199882651	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73039927	AATATTCATGAGGAT[-/A]ATCACAAAAGCAGTT	9873
rs199886576	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72898746	TTTTTTTTTTTTTTT[A/T]AAAGACAGGGTCTTG	9873
rs199889884	in-del	-/AAGCAGAG			intron-variant	FCHSD2	GRCh38.p7	11:72917004	TTTTTTTTTTTTTTG[-/AAGCAGAG]TGTTGCTCTGTCGCC	9873
rs199892054	snp	A/G	3.54497e-05	0.00420994	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73001104	CTGCATTGTTCCCTC[A/G]AGAAAAGATTTCCAA	9873
rs199959976	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73023582	CTCCTTCAACGGTGG[G/T]GGGAATGCAAAATAG	9873
rs199961304	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72896947	TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG	9873
rs199969266	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73045521	TTGGAACCAACCCAG[A/C]TGTCCAACAATGATA	9873
rs199986930	in-del	-/GGC	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72972751	CATAAGCCCCTTGTG[-/GGC]GGCACCAGAGAATAA	9873
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	9873
rs200038057	in-del	-/AGTTGTC			intron-variant	FCHSD2	GRCh38.p7	11:72923961	TAAATAAATAAATAA[-/AGTTGTC]TTTTTGTTGTTGGGT	9873
rs200056109	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73083570	AGAAAAAAAAAAAAA[-/A]CAAGAAAGAAATAAC	9873
rs200071474	in-del	-/A	0.0166325	0.0896639	intron-variant	FCHSD2	GRCh38.p7	11:73030103	AATGCCATTAGTTTG[-/A]AAATATTTTTGCCTA	9873
rs200093798	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73099280	TAAAACAACACAAAA[A/C]AAAACAAAAACAGAA	9873
rs200106413	in-del	-/T/TT/TTT	0.406641	0.194842	intron-variant	FCHSD2	GRCh38.p7	11:72914963	TTTTTTTTTTTTTTT[-/T/TT/TTT]GCAAACTAAGCATCT	9873
rs200107454	in-del	-/C	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:72883854	GGAGAATCGCTTGAG[-/C]CCAGGAGGTTCGGGC	9873
rs200108232	in-del	-/AAAAAAAAAAAAC			intron-variant	FCHSD2	GRCh38.p7	11:72845450	CTCAAAAAAAAAAAA[-/AAAAAAAAAAAAC]AACAACAAACAAACA	9873
rs200133588	in-del	-/A	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:72946547	CTTAAAGTATAATTT[-/A]AAAAAAAACTAGACA	9873
rs200153578	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72851499	TAATCCCAGCACTTT[C/G]GGAGGCCGAGGTGGG	9873
rs200159157	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73097615	TTTTTTTTTTTTTTT[-/T]CTAATTACTGATTCA	9873
rs200173029	in-del	-/CA			intron-variant	FCHSD2	GRCh38.p7	11:72871525	GGTTAAGTAAGGTTC[-/CA]CTTACTTAACCTAAG	9873
rs200198004	in-del	-/ATA			intron-variant	FCHSD2	GRCh38.p7	11:72890385	AGTAAGAACAAAACA[-/ATA]TAATAACAGCAACAC	9873
rs200234136	in-del	-/TTA	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73090761	ATATAATGCATGTTT[-/TTA]TTGAGATGAAATTCA	9873
rs200241574	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73132824	AATGAAACGGTAACA[A/G]AAAAAAAAAAAAAAA	9873
rs200250879	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73109396	TGTCCTCTTCAATTT[A/C]TTTCATCAATGTTTT	9873
rs200261651	in-del	-/CTGT	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:73108082	TGCCGGTGTTTGTTA[-/CTGT]CTGTCTTTTGGATAA	9873
rs200269084	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72978216	ACCTAATGTAAATGA[C/T]GAGTTAATGGGTACA	9873
rs200272080	snp	A/T	1.68071e-05	0.00289884	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72984133	GTAGCGATCCTGATG[A/T]GCATTTGCTGCCGCT	9873
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	9873
rs200346955	snp	C/T	0.000129738	0.00805309	intron-variant	FCHSD2	GRCh38.p7	11:72921957	ATCAAGAGCCTGTAA[C/T]AGAGGAGTAAATAAA	9873
rs200370813	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73067120	CTGGATAAAGAAAAT[A/G]TGGCACATATACACC	9873
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	9873
rs200382288	in-del	-/AA			intron-variant	FCHSD2	GRCh38.p7	11:72861396	TATTTAAAAACTTCC[-/AA]AAAAAAAAAAAAACT	9873
rs200382897	in-del	-/AG			intron-variant	FCHSD2	GRCh38.p7	11:73129703	CAATAAATGTAATGC[-/AG]ACTTGAATCATCCCA	9873
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	9873
rs200395290	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73026837	AATGGTTTAAAAGTT[C/T]GGCACTTCCCCCTTT	9873
rs200419528	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73106423	AAAAAAAAAAAAAAA[C/T]AAAAAGAAAAAAGAA	9873
rs200439027	in-del	-/TGTA			intron-variant	FCHSD2	GRCh38.p7	11:73035204	GTATGTATGTATGTA[-/TGTA]CGTACTAAGACAAGG	9873
rs200462571	in-del	-/GAGA	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72985678	TATTCTGAACTTACT[-/GAGA]AAGTCCTGGGACTCT	9873
rs200464991	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72935353	TCTTCAGCAATAAAG[A/T]TTTGCTGAAATCTCT	9873
rs200475196	snp	C/T			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143772	CCACATGACCAGAAA[C/T]TGAAAAGGTGGAACT	9873
rs200477185	in-del	-/TATG	0.129873	0.219248	intron-variant	FCHSD2	GRCh38.p7	11:73025993	TATAGAGATTCATTT[-/TATG]TATGTATGTATGTAT	9873
rs200499779	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72891427	GCAAAATAATCAATA[C/T]TCAAACTTAACCATC	9873
rs200508014	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72941468	TTAGTATAAAATATA[-/G]ACTCCCAACTCTATT	9873
rs200510857	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72890391	AACAAAACAATATAA[-/T]AACAGCAACACAATC	9873
rs200513826	in-del	-/A	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73024164	TAATATACGTAAATT[-/A]AAAAAAAATCTACCA	9873
rs200538165	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72907602	TAATCACGTGGGTTT[-/G]TTTTTTTTTTTTTTT	9873
rs200561815	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72979902	CAAAAGACAGTCATA[A/G]TGAGGGTTGTTATCA	9873
rs200567071	in-del	-/GCA			intron-variant	FCHSD2	GRCh38.p7	11:72910066	GAGCACCTCTGCCCG[-/GCA]GCCGCCCCATCTGGG	9873
rs200571034	in-del	-/CA	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73035692	CAGTACTGAAATGTT[-/CA]GTTTTTATTTATTTA	9873
rs200584717	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73014880	CTGGAGTCTCACTCT[G/T]TCGCCCAGGCTGGAG	9873
rs200589229	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72950593	AGACTATTCTTTCCT[-/C]CCACTGAATTGTTTT	9873
rs200590736	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72886084	CTCAAAACCTCTGGA[A/G]TTCTAAGGGGGTGTT	9873
rs200623024	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72866259	ACTCTGTTCTGTTTT[G/T]TGTTTTGTTTTGTTT	9873
rs200625859	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72923160	GTTGTACCACATTTT[A/G]TTTATTAATCAGGTG	9873
rs200661196	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72901865	TTAATTCTATTCTGG[-/T]TTTTTTTTTTGTTTG	9873
rs200661604	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72907497	ACTCTTATTATTTTG[A/C]GATATGTTCCAACAA	9873
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	9873
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	9873
rs200720258	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72968387	TTTGTTCAGAAACGG[C/T]TACTCCTCTCCAGAG	9873
rs200725859	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72906201	GATGAGCATTTTTTC[A/G]TGTCTGTTGGCTGCA	9873
rs200728959	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73110011	TTTGCATATGTTGAA[A/C]CATCCTTGCATCCCT	9873
rs200735136	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73064487	CTTCAAAAAAAAAAA[-/A]TCAATGAATCCAGGA	9873
rs200737760	in-del	-/T	0.0170251	0.090679	intron-variant	FCHSD2	GRCh38.p7	11:73097510	TTCCCTTTTCTTCTG[-/T]TTTTTTTGGAATAGT	9873
rs200753128	snp	A/G	0.000131955	0.00812157	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72988978	CTTTGCCTCGATGTC[A/G]GCTTTCTCTCGTACT	9873
rs200761582	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73057880	TGCCAATTCGGTATT[C/T]TTTTTTTTTTTTTTT	9873
rs200768834	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73087719	AAAAAAAAAAAAAAA[-/T]ATTTTTAAAATAAAT	9873
rs200774518	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72853505	CTGCAACCTCCGCCT[C/G]CCAGGTTCAAGCAAT	9873
rs200783836	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837813	TAGCAGTTGGTCTGG[A/C]CCAGCCACAGCCTGG	9873
rs200788964	in-del	-/T/TT			intron-variant	FCHSD2	GRCh38.p7	11:72907598	GAGATAATCACGTGG[-/T/TT]GTTTTTTTTTTTTTT	9873
rs200809431	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72925058	AGGCATCATGAGCTC[-/A]AAAAAAAAATAAGGC	9873
rs200814557	in-del	-/AA	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73086207	TGAGGCCAGGAGTTT[-/AA]GACAGGCCTGGCCAA	9873
rs200837586	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72873329	GTGAGACTCTGTTTC[-/A]AAAAAAAAAAAAAAT	9873
rs200855476	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72924680	GCTGTTCCATTAAAC[-/T]TTTTTTTTTTTTTTT	9873
rs200902127	snp	C/T	0.00299544	0.0385843	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843222	GACGTGTGTGACCGA[C/T]TGTCCAAAGCGGCCA	9873
rs200915587	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73006057	GGCCTACAGGCATGA[C/G]CCACTGCATGTGGCT	9873
rs200960351	in-del	-/ACTC	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73033654	CTATGTTAATTAAAT[-/ACTC]AAACTATGGAATTCT	9873
rs200962772	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72926195	GGAGGGCCTGAAGAC[A/C]GGGGGCTGGACTGCC	9873
rs200980735	in-del	-/A	0.0232847	0.105357	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142589	AGGTGTAGAAACGCC[-/A]AGCGCCACGCGAAAA	9873
rs201009553	snp	A/C/T			intron-variant	FCHSD2	GRCh38.p7	11:73105438	TCTTTATTTGGTAAC[A/C/T]TTACTTTCCTAGGGA	9873
rs201018083	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72962612	CCCCCTTTTTTTTTT[A/T]AACTAAGAATGTTCT	9873
rs201055524	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73085718	AACTTTTTAACTATT[-/A]AAAAAAAAAATCCCT	9873
rs201063455	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72890391	AACAAAACAATATAA[C/T]AACAGCAACACAATC	9873
rs201093762	in-del	-/A	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72947326	GGCCCACATCTGGCC[-/A]AGAGGAGCAGAACTG	9873
rs201145516	in-del	-/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841383	ATGCAGTTTTTTTTT[-/T]GCCCTTCAGGCGAAT	9873
rs201157171	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73109405	CAATTTCTTTCATCA[A/G]TGTTTTATAGTTTTC	9873
rs201158355	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73003665	CTAATTTTTTGTATT[C/T]TTAGTAGAGACGGGG	9873
rs201229145	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72995536	TGAAACCTCATCTCT[-/A]AAAAAAAAAGTACAA	9873
rs201245908	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72992099	TGCAAAAAATCACAA[A/G]CATTCTTATACACCA	9873
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	9873
rs201284616	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72984116	ACTAAATCTGTTTGA[C/T]AGTAGCGATCCTGAT	9873
rs201292605	in-del	-/TTTTTTGTATC	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72885208	ATTTTACTTAGGCTA[-/TTTTTTGTATC]TGTTAAGTGGAAACC	9873
rs201295990	in-del	-/GAA	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:72900031	TCCAGCACACCTGTT[-/GAA]GAAGATTAAGGTGCT	9873
rs201296902	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73065388	ATTTATGACAAACCC[A/C]CAGCCAATATCATAC	9873
rs201298041	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72965048	CCCGCCTTGGCCTCC[A/C]AAAGTGCTGGGATTA	9873
rs201300387	in-del	-/TTTA	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73097373	GTTTGTTTGGTTTAT[-/TTTA]TTTATTTATTTTTTT	9873
rs201315056	snp	A/G	0.000224052	0.0105819	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902570	ACAAGGCTGGAACTG[A/G]AAGGGCTGGGGTTTG	9873
rs201318726	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73117149	ATAAGCTGGTACTTA[C/T]AACAAATACATTCTA	9873
rs201339205	in-del	-/GGC			intron-variant	FCHSD2	GRCh38.p7	11:72975759	TGCCATACAGAAAGA[-/GGC]TGTTTATCTTTTATT	9873
rs201356134	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73100877	GATTTTTTTTTTTTT[C/T]CTTAATGCTGTTTAG	9873
rs201357306	in-del	-/T	0.0232847	0.105357	intron-variant	FCHSD2	GRCh38.p7	11:73041587	GGATAATTTATGGAG[-/T]TTTTTTTGTTTGTTT	9873
rs201364368	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73080320	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA	9873
rs201371746	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72921085	GACAAAAAAAAAAAA[-/A]TTGAACTGGATCTTT	9873
rs201374616	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72920068	TATAGGATCTAAATA[A/G]AAAAAGAAGCTTGAG	9873
rs201376447	in-del	-/A	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73016149	CTCTACCAAAAATAC[-/A]AAAATTAGCCGGGTG	9873
rs201405233	in-del	-/TTTG	0.0391387	0.134304	intron-variant	FCHSD2	GRCh38.p7	11:73041604	TTTTTTGTTTGTTTG[-/TTTG]CTACTGAGTTGAGTT	9873
rs201459401	in-del	-/TTTT			intron-variant	FCHSD2	GRCh38.p7	11:73035695	TACTGAAATGTTCAG[-/TTTT]TATTTATTTATTTAT	9873
rs201464402	in-del	-/AA			intron-variant	FCHSD2	GRCh38.p7	11:72908338	AATAGTGCTGCAATC[-/AA]CATGAGAGTGCAGAT	9873
rs201465503	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72989418	ACTGTTGGAGATATC[-/A]ATGATAATAAAATCA	9873
rs201473940	in-del	-/CG			intron-variant	FCHSD2	GRCh38.p7	11:73049726	GAAAGAGAGACACCT[-/CG]GAAGAGTTGGATAAT	9873
rs201512091	in-del	-/CAAA			intron-variant	FCHSD2	GRCh38.p7	11:72855314	AAACAAACAAACAAA[-/CAAA]AAAGACCAAAAAGTT	9873
rs201515010	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72902068	TTAGTAGAGACAGGG[-/TT]TTGTCATGTTGGCCA	9873
rs201565404	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72906832	GTTACTGTAGCCTTG[C/T]AGTATAGTTTGAAGT	9873
rs201579323	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73116960	TTTCCCCAAAAAAAA[-/T]CACTATTGTTATATC	9873
rs201596756	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72866261	TCTGTTCTGTTTTTT[G/T]TTTTGTTTTGTTTTT	9873
rs201598501	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72985609	ATTATTTCCACCATT[A/G]AAAGTACTTCTTGTT	9873
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	9873
rs201618443	in-del	-/A	0.0295035	0.117819	intron-variant	FCHSD2	GRCh38.p7	11:72866744	CCTTTTTAAATGTGC[-/A]AGTGTATTCTCATTA	9873
rs201620143	snp	A/G	0.000229183	0.0107023	intron-variant	FCHSD2	GRCh38.p7	11:73000965	GATATTAAAATGCAT[A/G]TAAGAACAGAAATAA	9873
rs201627189	snp	C/T	8.50593e-05	0.00652092	intron-variant	FCHSD2	GRCh38.p7	11:72985050	TGTGAAATACACTTA[C/T]TGAAAACTTACCTTT	9873
rs201639046	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72913821	AAAAACCAAAAAAAA[-/C]CCCAAAAAAAAAACA	9873
rs201655074	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72992384	ATCAAGCTACCAATG[A/C]CTTTCTTCACAGAAT	9873
rs201660154	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72924696	TTTTTTTTTTTTTTT[-/T]AAATACACAAATTCT	9873
rs201676944	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73109378	TATCTTTCCATTTGT[C/T]TGTGTCCTCTTCAAT	9873
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	9873
rs201721901	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72900687	GATTAAAAAAAAAAA[C/T]CACTACTATAAAGGG	9873
rs201725751	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72991338	ATCAATAGAAAAAGA[C/G]GGAATCCTCCCTAAC	9873
rs201734419	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73109343	AACAATATTGATTCT[C/T]CCAATCCATGAACAT	9873
rs201739186	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73016168	ATTAGCCGGGTGTGG[G/T]AGCATGCGCCTGTAG	9873
rs201755122	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967698	GAGATAGTGGTGATG[A/G/T]TTGTACAACCTAGTA	9873
rs201756436	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73120820	CTCACAGTCTGGAGG[G/T]GAAGATATACCAAAA	9873
rs201765729	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73103222	CTCTGTACACTTAAG[C/T]TAGATGGATTTTATT	9873
rs201774717	in-del	-/ATTTCT			intron-variant	FCHSD2	GRCh38.p7	11:73097671	CACTTGTTATTGAGA[-/ATTTCT]ATTTTTTTCTGTAAT	9873
rs201775859	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73071535	TTTCTACTAAAAATA[-/C]AAAAAAAAAAAAAAA	9873
rs201783308	in-del	-/A	0.281313	0.248031	intron-variant	FCHSD2	GRCh38.p7	11:72928841	TCGTCATTTAGCATT[-/A]AGGTATATCTCCTAA	9873
rs201791287	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72960572	CATAATACTTCTTGG[C/T]CCAGTGTTCCATGCA	9873
rs201795040	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72892622	TGTTTTTTGTTTTTT[-/T]GAGACAGAGTCTCAC	9873
rs201818849	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73097396	TTATTTTTTTTTTTT[-/T]GCATCTCTCTTCACA	9873
rs201841322	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73082151	GACCATCCTGGCCAA[A/C]AGGGTGAAACCCAGT	9873
rs201858110	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72896614	TGGAATAAGTAGAAC[A/G]AAAGTCCCAAGGGAC	9873
rs201864880	snp	A/C/G	0.00819378	0.0634803	intron-variant	FCHSD2	GRCh38.p7	11:72947756	AAAACATAATTTTCT[A/C/G]ATAAAGAAAATTAAA	9873
rs201865960	snp	C/G	0.000214145	0.0103454	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72849810	CTTAAGGTGCCAGAA[C/G]GGCTGGAACTGCTGT	9873
rs201894941	snp	A/C	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:72943830	GTTAGCACATCTATA[A/C]TTAAATATTTGTTCT	9873
rs201895006	snp	A/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72883949	AAAAAAAAAAAAAAA[A/T]TTTTTTTTAATGAGG	9873
rs201906618	in-del	-/TA	0.0448719	0.142907	intron-variant	FCHSD2	GRCh38.p7	11:73025277	ATAAAGAAAATGTGG[-/TA]TATATATATACCATG	9873
rs201914151	in-del	-/TAAA	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72882715	AGGAAACAGAGTGCC[-/TAAA]TAAATAGAGAGACAC	9873
rs201946674	snp	C/T	2.78765e-05	0.00373329	intron-variant	FCHSD2	GRCh38.p7	11:73015915	ATATTTTTTCTAAAA[C/T]AAATATTATGCCATA	9873
rs201952781	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73086263	AAAATACAAAAATTA[G/T]CTGGGCGTGGTGGTG	9873
rs201956100	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72978176	TGGGGTGGGGGGAGC[A/G]GGGAGGGATAGCGTT	9873
rs201970337	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72946041	CCCAGCCATTCCATT[A/T]CCGAGTATATACTCA	9873
rs201980141	in-del	-/GTATGTAC			intron-variant	FCHSD2	GRCh38.p7	11:73035198	TATGTATGTATGTAT[-/GTATGTAC]GTACTAAGACAAGGT	9873
rs201980904	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72907620	TTTTTTTTTTTTTTT[C/T]TTGAGACGGAGTCTG	9873
rs202001987	in-del	-/TGAATGCTT	0.0341408	0.126114	intron-variant	FCHSD2	GRCh38.p7	11:72907442	GCTTCCAGTTTTTGC[-/TGAATGCTT]CCATTCAGTATAATA	9873
rs202043775	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72973218	ACTAAAAATACAAAA[G/T]TAGCTGGGTGTGGTG	9873
rs202050835	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72975897	ATTAAATTGACGTTT[C/G]TTCTCTTTTCTACTA	9873
rs202075634	in-del	-/AA	0.0356815	0.128715	intron-variant	FCHSD2	GRCh38.p7	11:72873074	GTGGCTCATGCCTAT[-/AA]TCCCAGCACTTCGGG	9873
rs202083118	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72941481	AGACTCCCAACTCTA[-/T]TTAATATATTACTTA	9873
rs202108873	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73116948	AACCTTTCCATTTTT[-/C]CCCAAAAAAAATCAC	9873
rs202109035	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73017277	AGTCACCAAACCTGG[-/C]CAACGTATTACTTTT	9873
rs202112144	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73100876	GATTTTTTTTTTTTT[-/T]CCTTAATGCTGTTTA	9873
rs202119912	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73063047	CAGAGAGAAAGGTCA[G/T]GTTACCCACAAAGGG	9873
rs202144556	snp	C/T	4.98194e-05	0.00499071	intron-variant	FCHSD2	GRCh38.p7	11:72849910	AAAAATTAGAAACCA[C/T]TGGCTAGTTTCCTTA	9873
rs202178689	snp	C/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840890	ACAGGTCGCAGTTTG[C/T]CATATGAGGTCTCAG	9873
rs202179623	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73126336	CAGGGCAAGATTCCA[A/T]CTTAAAAAAAAAAAA	9873
rs202185212	snp	C/T	8.86486e-05	0.00665706	intron-variant	FCHSD2	GRCh38.p7	11:72902658	AGAGAAAATAAAATA[C/T]CTTTAGGTCTTTAAT	9873
rs202202871	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73085914	ATTCAAAGGGGAAAA[A/C]AAGCCAATACAAATT	9873
rs202226782	in-del	-/TTT			intron-variant	FCHSD2	GRCh38.p7	11:72851878	ATCAGTCAGAGTGGC[-/TTT]TTTTTTTTTTTTTTG	9873
rs207472005	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73032357	CCTCGGCTTCCCAAG[A/G]AACTAATATTACAGG	9873
rs367550753	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73066911	TACTTCAACCATTGT[A/G]GAAGACAGTGTAGCG	9873
rs367582930	in-del	-/AGA			intron-variant	FCHSD2	GRCh38.p7	11:72900036	CACACCTGTTGAAGA[-/AGA]TTAAGGTGCTTCACA	9873
rs367632709	in-del	-/A/AA			intron-variant	FCHSD2	GRCh38.p7	11:73132824	ATGAAACGGTAACAG[-/A/AA]AAAAAAAAAAAAAAA	9873
rs367639909	snp	C/T	3.48693e-05	0.00417534	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72889941	TCTGATTCTAACTGT[C/T]GGCTCTACAATACAA	9873
rs367666447	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72992251	CAAACCACTGCTCAA[G/T]GAAATAAAAGAGGAT	9873
rs367683290	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72924744	TAATAAAGCTGCACC[G/T]TCTATAGTGCTTACA	9873
rs367685476	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73090110	TTGTGTTGGGATAAC[C/T]TGATAGGAAGATCTA	9873
rs367685737	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73002431	AACGAATGCTCTCCA[C/T]GGCCTCACTGCATGA	9873
rs367689342	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73112725	ATGATCTCAGCTCAC[C/T]ACAACCTCTGCCTCC	9873
rs367695555	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73029090	GACCAGAAAGGGCAC[C/G]ATAAATATAATGGTG	9873
rs367695760	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73000745	ATTATGCCGAAAAGC[A/G]GTATTACTAAAAAGT	9873
rs367699025	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73130379	CAAGGACTACAGGCA[C/T]GTGCTATGGTGCCAG	9873
rs367701194	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73099145	CACCGAGCCCAGGCG[C/T]TCCAGGTTGCAGTAA	9873
rs367734791	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73123380	ACAATGCATATTAAA[C/T]GGTGGTAACTCCTGG	9873
rs367734833	in-del	-/CCTTCTCATTC			intron-variant	FCHSD2	GRCh38.p7	11:73096049	AACAAAACAAAAAAA[-/CCTTCTCATTC]AAAAATAAACCACCA	9873
rs367745075	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73091715	TTGGAATTTCCTCCC[A/G]TTATTTGGCCTAACT	9873
rs367771000	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73062318	AAGGTACACAAATCC[A/G]CAAAGATGGGGAGAA	9873
rs367780229	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72917694	AGTTCAAGACTAGCC[C/T]GGCTAACATGACGAA	9873
rs367780871	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72932064	AGTTCCTCAGTGTGT[A/G]ATGCCACTATTCACT	9873
rs367784456	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72960768	GGGCAAGGGACAGGG[A/C]ATAATAAAGAACCCC	9873
rs367786674	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72996235	ACTCTGTTATTTACT[A/G]CCTAAGTCTCTTTAA	9873
rs367801051	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73017320	ATGTGGTCCCCTAAC[A/G]CTATAACAGGGCCTA	9873
rs367811851	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73006187	TCTGGGATTACATAC[A/G]TGAACCACTACTCTC	9873
rs367816005	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72956232	AACAAGCACATAAAT[A/G]GCAGAGAATAGAAAC	9873
rs367825165	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72928393	TGTTCTCTGCATTAT[A/G]CTCTACTTCCCAACT	9873
rs367837031	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72897124	AGGCGTGAGCCACCA[C/T]GCCCGGCCGTCCTGT	9873
rs367867112	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73070557	GCCTCCTGAGTAGCT[A/G]GTATTACAGGCGCCT	9873
rs367872795	in-del	-/TTCT	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73111370	CATTATACAATGACC[-/TTCT]TTGTCTCTTCTAAAA	9873
rs367876577	in-del	-/G			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143002	CTACTCTCCCTACCA[-/G]CTAGATGTGCGCGAG	9873
rs367886976	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72870078	TGCGTGCCTGTGTGC[A/G]TGCCAGTCCCTCTGT	9873
rs367895469	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72847771	GATCTTGGCTCACTG[C/G]AACCTCCTCCTCCTG	9873
rs367901975	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73109731	TAGGACTTCCAGTAA[C/T]ACACTGAGTAACAGT	9873
rs367903852	in-del	-/TG			intron-variant	FCHSD2	GRCh38.p7	11:72931113	TTTTTTTTTTTTTTT[-/TG]AAAAGGAGTCGCGCT	9873
rs367905842	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72934804	ATATACTTAAAAAAA[C/T]AGCCAAACTTTTTGA	9873
rs367915822	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72917917	AAAAAATTGAGGACC[A/G]GCTTTTCCATTTCTG	9873
rs367926797	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72861473	GAAGACGAAATTCCA[C/T]ACAATTCTACACAAG	9873
rs367927694	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72947760	CATAATTTTCTCATA[A/T]AGAAAATTAAATACA	9873
rs367928077	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73011345	CTACCTTCTGAGCTG[-/G]AAGCCTAGGCTAGCA	9873
rs367939016	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72991142	TCCTCGACACATACA[C/T]CCTCCCAAGACTAAA	9873
rs367943180	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72950715	CTTTTAGGATATTTT[A/C]ATTTTTCATTTATAA	9873
rs367964796	in-del	-/C			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143967	AGGGAAGGCCTGGGG[-/C]AAGGGGACAGGTGGA	9873
rs368003593	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72903845	AGTAGTAGGTGTATA[C/T]TGCATTTTGTTTACC	9873
rs368008403	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870508	TGCCATTCAATGATA[C/T]TGAGTTATAAACTAC	9873
rs368008664	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72943552	TGAAAGGGAAGGAAA[C/T]TGAAGAGAATGACAG	9873
rs368010371	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72900316	TATCCACCAGTTGGG[C/T]GGCTTTTAAACTCTG	9873
rs368024554	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72965475	CTACTTCTATAAAGC[C/G]TTTTGTGACTTTCCT	9873
rs368035510	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72896398	TTCCCATCCCAGCTT[C/T]GCTTTGTCCTTTTTC	9873
rs368050578	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72994688	GGAGAATGGCTTGAA[C/T]CCAGGAGGTAGAGCT	9873
rs368051476	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73001677	CGCGGCTGGAAAAAT[A/G]TATCATGAACAACTG	9873
rs368062555	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72959811	ATGCTGATGAGCAGA[A/G]GTAGAACTATACTTC	9873
rs368085784	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72944336	CAGAAAAGGCCTTTG[A/G]CAAAATTCAACAACG	9873
rs368106300	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73082607	AAAGCCTAAAAGAGT[C/T]ATGCCCCAATCTCTC	9873
rs368123466	in-del	-/GA			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842252	GCTCTGACAGTGAGG[-/GA]GAGAGAGAGCCAGCT	9873
rs368134636	snp	C/T	0.000154888	0.00879886	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840858	TGCATTCGATAATCC[C/T]GCAAGATCAGAGACT	9873
rs368161429	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73033904	TTGAAACATGATGGT[A/G]AACAACGCTTATGAC	9873
rs368191101	in-del	-/TTTA			intron-variant	FCHSD2	GRCh38.p7	11:73035697	CTGAAATGTTCAGTT[-/TTTA]TTTATTTATTTATTT	9873
rs368232959	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73057277	CCTAGGACACAGTAC[A/G]CAGGTTCGAAGCATG	9873
rs368243277	in-del	-/GC			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841365	AAAAAAAAAAAAAAA[-/GC]AAATGCAGTTTTTTT	9873
rs368246136	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72973239	GGGTGTGGTGGCATG[C/T]GCCTGTAATCCCAGC	9873
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	9873
rs368267125	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72992785	AAGACTTAAATGTTA[-/G]ACCTAAAACCATAAA	9873
rs368271488	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73107261	GGTTTCACCATGTTG[C/G]CCAGGATAGTCGATC	9873
rs368273321	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73006656	TTACAGCAATTGCTG[C/T]GCAATCACTTCTTGG	9873
rs368296357	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861817	ATGCCTATAATCCCA[A/G]CTACTTGGGAGGCTG	9873
rs368324915	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73131256	GGCGCAGTGGTTCAC[A/G]CCTGTAATCCCAGCA	9873
rs368332938	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73016147	ATCTCTACCAAAAAT[A/G]CAAAAATTAGCCGGG	9873
rs368333075	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72877348	AAGATGGAGGTTCTG[C/T]TTAAATTCTGGTTGT	9873
rs368367894	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72969600	AATACAAGAAGCATC[A/G]AAGATATAAAAAACA	9873
rs368402914	snp	A/C			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143969	GGAAGGCCTGGGGCA[A/C]GGGGACAGGTGGATG	9873
rs368406708	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084446	CCTAGGCTTGAGTGC[A/G]GCGGTGAGGTCCTAG	9873
rs368407877	snp	G/T	1.64893e-05	0.0028713	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72887567	TGACACTCCAGATCA[G/T]TTAGAACCTATTAAA	9873
rs368418620	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905849	ATCATTGATGGACAT[C/T]TGGGTTGGCTCCAAG	9873
rs368439520	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72870867	ATTGCGCCACTGCAC[A/T]ACAGCCTGGGTGACA	9873
rs368443132	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72910300	TTTGTCCGGCCGCCC[C/T]GTCTGGGAGGTGTAC	9873
rs368448051	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72988346	TTGCTTTATATCACC[C/T]TCTATTACCAGTTGC	9873
rs368454241	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840234	TCATTTGGGATAAAG[A/G]CTCAAGTCCTTAAGA	9873
rs368461314	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73057423	TTACTGTGGTAATTA[C/T]GGGGGTTCCCAGCTT	9873
rs368461885	snp	A/C			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143495	GCACCCCACCACCAC[A/C]CATGAACCTTCCTGC	9873
rs368461952	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72978425	GCATATAAAAAGGTG[C/T]TCAATATCATTGACC	9873
rs368463095	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72898485	TTCAAACTATAAAAT[A/T]CAAAATAAAAGAACA	9873
rs368466459	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73069858	TTCATAAATGATACA[C/T]TGGTCTCATTCCACA	9873
rs368475839	in-del	-/AC			intron-variant	FCHSD2	GRCh38.p7	11:72871526	TTAAGTAAGGTTCCA[-/AC]CTTACTTAACCTAAG	9873
rs368488720	snp	A/G	0.0015437	0.0277393	intron-variant	FCHSD2	GRCh38.p7	11:72868075	CTTTTATTATTCACA[A/G]TAGCAAAGATAAGGA	9873
rs368503360	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72917185	AGATGAGGTTTCACC[A/G]TATTGGCCAGGCTGG	9873
rs368517276	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73113327	GGTACCTTAGTTTGG[C/T]TGATCATCATGCTTC	9873
rs368528340	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72868857	TTGCACAACTGTATT[A/C]TTGGTGGCAATGCAG	9873
rs368530743	in-del	-/GTCTCAG			intron-variant	FCHSD2	GRCh38.p7	11:73134481	TCTCAAAAAAAAAAA[-/GTCTCAG]AACATCCATAAACAG	9873
rs368541963	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73123303	TCCTGCAGTATCTCC[C/T]AGCCAAGCCAGTATT	9873
rs368544385	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72896890	GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC	9873
rs368549352	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72931550	GCAGGTGGATCACAA[-/C]GGTCAGGAGTTCAAG	9873
rs368558079	snp	C/T	0.000167986	0.00916323	intron-variant	FCHSD2	GRCh38.p7	11:72985014	CAATTCTCTGTTTTA[C/T]AAGCTAAGAGGTTTC	9873
rs368565080	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72962844	AGATTACAGAACTGC[C/G]ACAAAAGTTAAATAT	9873
rs368604322	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72853375	TAAGCCTATGAAACT[G/T]TAAAAGAAAACACAG	9873
rs368608709	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72984909	GGGTGCAAAACCCCC[-/C]ATGAACTGGGAGGGA	9873
rs368613716	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72949345	ATCACAGCTACTCAG[C/G]AGGCTGAGACAGGAG	9873
rs368644886	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108662	CAAGCTCCGCTTCCC[A/G]GGTTCACGCCATTCT	9873
rs368647135	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72889542	TGGCAAGACCCTATC[C/T]CTACAAAAAATCTAA	9873
rs368659761	snp	A/G			missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72849840	TCATCGAAAACATCC[A/G]TGTTATCTTCAAACT	9873
rs368669408	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72989689	GGAGAAGGGATGGAC[A/C]TAACAACTAAAACAA	9873
rs368677495	snp	A/G	4.99671e-05	0.00499811	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72889895	TTTTCGAGCTTCCTT[A/G]TTTAGACTGTGCTCC	9873
rs368696879	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72997216	GCAGCTACACGATGT[C/T]GAGAAGACAAAGGTT	9873
rs368726413	in-del	-/CC			intron-variant	FCHSD2	GRCh38.p7	11:73004436	CCTCCTGATTCTACT[-/CC]CAAACCCTTTAGAAT	9873
rs368736333	snp	A/G	0.000199727	0.00999118	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841416	GTAGGTTTCTGAAGT[A/G]AAAATGCATTTAGAC	9873
rs368745203	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72911114	CTTTTAGTAGTTTCA[C/T]AGTTTGAGGTCTTAG	9873
rs368746768	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72929072	ATTTTTTATGGCTGG[A/G]TAGTATTCCATGGTG	9873
rs368763998	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73132122	TGAAGAGGCAATGAC[A/G]ACTGCATCACAGCCT	9873
rs368765590	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73119684	ACTCCTGGCTTCAAG[C/T]GATCCTCCCACCTTG	9873
rs368775478	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73102438	ACAAATGTGTACAAA[A/G]TGTGTACAGCAGCAT	9873
rs368795801	in-del	-/AGGA			intron-variant	FCHSD2	GRCh38.p7	11:72966203	TCACTCTGTCGCCCA[-/AGGA]GGAAGGAGTGCAGTG	9873
rs368803817	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73094473	ACAAAAATATTTATA[A/C]CATCTTTAGTCATAA	9873
rs368859921	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72968299	CTTAAGACTGATAGA[C/T]CTTTGCCTTTTAATT	9873
rs368864043	in-del	-/AA			intron-variant	FCHSD2	GRCh38.p7	11:73076958	CTCTACTAAAAATAC[-/AA]AAAAAATTAGCCAGG	9873
rs368880489	snp	A/C/T	0.000356943	0.0133553	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73001048	GGCTCAGAAATGAAG[A/C/T]TTTTATAGTTTTCAC	9873
rs368911084	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73054382	CAGACAGGGGGCTAG[-/A]AAAAAAAAAGAAATT	9873
rs368911938	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72907540	TGAGAGTTTTTAGCA[C/T]GAAGGGCTGCTAAAT	9873
rs368915774	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72885470	AGTCTAGTTTGGCAT[A/G]CTATGGAAATAATAG	9873
rs368915914	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73077444	AGCACCTAGAACTCA[A/C]ATACACAGCTGGTGG	9873
rs368935748	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72938815	CTTATCAAGCTAACC[C/T]AAGACTAATTTATCA	9873
rs368938666	snp	C/T	0.0174175	0.0916809	intron-variant	FCHSD2	GRCh38.p7	11:73096419	AGCCAGATGTGGTGG[C/T]GGGCGCCTGTAATTC	9873
rs368967084	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72874742	TTAGACTGCAGTCCC[A/G]GAATTAAACACTGCT	9873
rs368981030	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72873202	GACACGGTGGCGGGT[A/G]CCTGTAATCCCAGCT	9873
rs368983956	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72966615	TGATGCAAACAGATT[C/G]CTGCATGAATACATT	9873
rs368984181	in-del	-/GA			intron-variant	FCHSD2	GRCh38.p7	11:72885240	TGGAAACCAAGWGAG[-/GA]AKTATTTTATGCTAA	9873
rs368989172	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006330	CAAAACTAAATTCTT[C/G]ATTTCCCTAAAATCT	9873
rs368995456	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72929298	CTGAGGAATAGAAGC[C/T]ACTTTCAATGGAGAT	9873
rs369015175	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73029817	TTAGTAAGTCACCAC[A/T]ATATACAGAGAAAGG	9873
rs369020177	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72879906	TGAGAGACTGAGGCC[A/G]AACAATCGGTTGAAC	9873
rs369020667	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73078512	AACTACTACTACATG[C/T]AACAACATGCATGAA	9873
rs369023201	in-del	-/T	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73043274	TGAAGGAATTTTTAC[-/T]TCTCTTCATCACAGA	9873
rs369024565	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72884354	TTCTGTATGTTTGAA[A/C]ATTTTCAGTAAAAAA	9873
rs369032350	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72854854	AAAGAATACTAGAAA[C/T]GGGCCAGGCACGGTG	9873
rs369033136	in-del	-/ATG	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73118701	ATGTGATCAGAGAAT[-/ATG]ATGATACTATAATGA	9873
rs369033928	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72907814	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG	9873
rs369035653	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72894269	ATATACTGGGGCTGG[A/G]CACAGTAGCTCACAC	9873
rs369038418	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72981061	TCAATGGTGGAAATT[C/T]ACTAAGTAGCTAACA	9873
rs369044485	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73030571	AGGTCTCTTACCTGA[C/T]GACCTTAACTTTGTA	9873
rs369046018	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72998868	CCTTGTGCACTGTTG[A/G]TGGGAATGCCAAATG	9873
rs369049901	in-del	-/TCTTT			intron-variant	FCHSD2	GRCh38.p7	11:72888650	GGAGACAGGGTCTTT[-/TCTTT]CTCTGTCACCCAGTC	9873
rs369060852	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72992603	CTCAGAAATAATGCC[A/G]CATATCTACAACTAT	9873
rs369071419	snp	A/C	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73132234	AACTTCCTTTTGTAC[A/C]TTGAATAAGACAACA	9873
rs369077477	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73050532	AATAGTTCCTTTCGT[A/G]GGACAACATTGGAGT	9873
rs369082709	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72931749	TAGTCTGGGTGACAG[A/G]GCAAGACCCTGTCTC	9873
rs369095699	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72873023	TTTGCATTTTCCTGG[A/G]TAACTATTAATGTTA	9873
rs369095812	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72864785	TTGTCATCTTGGTAT[A/G]GCTTTTGAATAAGAG	9873
rs369135921	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73035246	CACCCAGGTTGGAGC[A/G]CAGTGGCGCGATCTT	9873
rs369144556	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73048970	AGAGCTATGAAGAAC[A/G]GTAAATATTTAAATA	9873
rs369175013	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73108818	CCTCATGATCCACCC[A/G]CTTCGGCCTCCCAAA	9873
rs369185909	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73043335	GAAGATAAATATTAT[A/C]AGTTTCCATAAGCAA	9873
rs369207284	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72906138	CATTCTGTTGTGACA[C/T]AGTATCTCATTGTGG	9873
rs369215343	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73036862	ACAATTTTCTGTAAT[A/G]CACATATTCTGCTTA	9873
rs369215706	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73039249	TTCTGCAGGGTGCAG[G/T]GCTCACACCTGTAAG	9873
rs369219061	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72871888	TGAACTGCTGTGCCC[A/C]ACAGGTACATAATTT	9873
rs369263755	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901083	TCAAGGACGATTACT[C/G]TATGCTTTTAAACAA	9873
rs369274428	in-del	-/TTAAGTAAGGTTCC			intron-variant	FCHSD2	GRCh38.p7	11:72871512	TAAGCTAATTTTAGG[-/TTAAGTAAGGTTCC]ACTTACTTAACCTAA	9873
rs369285667	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73004439	TCCTGATTCTACTCA[A/G]ACCCTTTAGAATTCT	9873
rs369289700	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930442	AGAGATTCATCTCTA[C/T]ATTTTCTTTGACTTC	9873
rs369295273	snp	C/T	4.63639e-05	0.00481454	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72921877	TTCTGCACAGCTTGG[C/T]ATGTTTCTAGCTCAG	9873
rs369300695	snp	C/T	8.24205e-05	0.00641899	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843376	CACACACAATTTAGA[C/T]AGGGCACAACAAAGA	9873
rs369303085	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842367	GTATGTCACATATAA[C/T]TTGGCATTTTGGTTA	9873
rs369305227	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73004182	TCTACATATCACATG[A/G]TAAGTACTACGTTAT	9873
rs369313444	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858148	AGAATCTGGTAATAC[C/T]TAATACAGAGGAAGA	9873
rs369313931	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73006196	ACATACATGAACCAC[C/T]ACTCTCAGCCCAATT	9873
rs369315223	snp	A/T	0.000268276	0.0115787	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841497	CAGGGAGCTCCTCTT[A/T]TCTGGGCTGGGGTAG	9873
rs369316091	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73051856	ACCTTCAGGATGCTA[A/C]CACGGTATATAAACA	9873
rs369322682	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73016396	ACACTACAACCTTTT[C/T]TCATTATTGTCCAGT	9873
rs369344558	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72983085	GGATCACGAGGTCAG[C/G]AGATCGAGACCATCC	9873
rs369363765	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72937388	ATCAAAGTATTGAAC[C/T]GACAGAAAGCATTTA	9873
rs369393504	snp	A/C	0.000629822	0.0177346	intron-variant	FCHSD2	GRCh38.p7	11:72902498	GTTACTTAAGCACAA[A/C]CACAACTGAACAACA	9873
rs369415482	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73118365	AATGGCACTATCATC[C/G]CAAAAAGTTTCCTCA	9873
rs369441390	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72997507	ATAACCAAAAATCAA[C/G]AAAAACCGCAGGCGG	9873
rs369449969	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72937748	AGAACCTGGGCAAGC[A/G]TTGGAAACAAACAAA	9873
rs369458748	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73071566	ATTAGCTGGGCATGG[G/T]GGTGTGTGCCCGTAG	9873
rs369468492	snp	C/T	0.000153988	0.00877327	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843427	TGTCACAAGAAAGGG[C/T]GATATGAGCAAAGGA	9873
rs369497265	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73079354	GGTACCCGCCACGAC[A/G]CCTGGCTAATTTTTT	9873
rs369507203	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73044053	AAACAATTAGCCTAT[C/G]CAAATGAACACAGTA	9873
rs369513274	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73010746	AGGACTGGGGCACCA[A/G]GTAGGCCAGTCTTTG	9873
rs369537734	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73019115	CATCTAAATGACATG[A/G]TAGTGACTTTTTCAG	9873
rs369546889	snp	A/G	0.00358779	0.0422022	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73141935	AAGGACCAGGAGGAG[A/G]AGGAGGGCCGGAGAG	9873
rs369552692	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72899950	TACCGTATGACTCTG[A/G]ACAAGTCTCCCTTAC	9873
rs369559627	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73040758	ATGTATTCTAATTAT[G/T]TTGAAAGACATATTG	9873
rs369562211	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73124193	CATGTTCTCACTCAT[A/G]GATGGGAATTGAACA	9873
rs369593900	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73096730	ACTGTGAGCTTGTCA[C/T]ATGTGCCCTTTAACA	9873
rs369608429	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73052142	TTTCCTTTGGTATAT[A/C]TGTGATCTGAACATG	9873
rs369614111	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73101365	ATCTAAGTTCAGAGA[A/G]AGGAGTGATAACTCT	9873
rs369617685	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908530	CCCTTTTCTCCACAT[C/T]CTCACCAGCATCTGT	9873
rs369620863	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73069169	TACAAAAATTAGCCA[G/T]GCGTGGTGGCATGCA	9873
rs369627062	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019730	ACTCTGGGGCTATTA[C/T]AGTAAAGGTCCTAAA	9873
rs369636857	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73072302	TACGAGATGTGCTAC[C/T]GAATAGCCATGAAAA	9873
rs369639708	in-del	-/AT			intron-variant	FCHSD2	GRCh38.p7	11:72887077	TCCTAAGCTCTGAAA[-/AT]ATATATATATATATG	9873
rs369649475	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72992479	AAAAGAACAAAGCTG[C/G]AGGCATCACACTACC	9873
rs369674043	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72901291	GGCCCCAGCTAATCG[G/T]GAGGCTGATGTGGGA	9873
rs369695601	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72945659	TACTCATCTGACAAA[C/G]GGCTAATATCTAGAA	9873
rs369700486	snp	A/G	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73066821	TGGCGATCATTAAAA[A/G]GTCAGGAAACAACAG	9873
rs369705103	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72949567	GCCTGGCAACCACTA[A/G]TCTACTTTCTACATT	9873
rs369711968	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73104480	TCACCATGTTGGCCA[C/G]GGTGGTCTCAAACTC	9873
rs369713004	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124177	AGAAAACCAAACACC[A/G]CATGTTCTCACTCAT	9873
rs369718040	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73017958	ATCCCTCATGAACTA[C/T]CTGGTTATATTGAGA	9873
rs369720865	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73065539	AAGAAATAAAAGGTA[C/T]TCAAATAGGAAGAGA	9873
rs369749417	in-del	-/AACAT			intron-variant	FCHSD2	GRCh38.p7	11:73106632	TAAATACAGTAACAT[-/AACAT]TTCCATAAAAAATGG	9873
rs369765858	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72914514	GGCCACAGCAACCAA[A/G]CAGCATGGTACTAGT	9873
rs369766908	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028502	TTGATTTTACAGGCT[C/T]ACAGGCAGAAGGGAC	9873
rs369773160	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72915277	TTGTGGAGAAAAAGG[A/C]ACACTTTTACACTGT	9873
rs369794395	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73116996	TTCATTTTTAGCATA[C/T]TGATTTTTATTACTC	9873
rs369813919	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72855348	GGGTGTGGTGGCAGG[G/T]GCCTGTAATCCCAGC	9873
rs369816755	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72855475	GTGAGACTCCATCTC[-/A]AAAAAAAAAAGAGTT	9873
rs369827007	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73094177	GACCACGCCAATGCA[C/T]TCCAGCCTGGGCTAC	9873
rs369829973	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72893748	GGAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAC	9873
rs369839004	snp	C/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73029924	TAATCAAAAACAAAA[C/G]AAAAACAAAAACAAA	9873
rs369841182	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73048020	CTATATTGTTTCTTT[-/T]AAGTAGTACATACTG	9873
rs369861585	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72892663	AGGCTGGAGTGCAGT[A/G]GCATGATCTCAGCTC	9873
rs369874613	in-del	-/TATATATAAGATCATATATATAGTTTA	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:72884531	TAATCATACATAGTT[-/TATATATAAGATCATATATATAGTTTA]TATATATGATGATAT	9873
rs369887017	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72954079	TGGCTATTACGCAGA[A/G]AATAGACATAAAGGT	9873
rs369899455	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72986187	TTTTTTACCTTGTCA[C/T]AGTCATATTTCATAA	9873
rs369930628	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72866149	AAGTGGGCCTGGAAT[G/T]TGCTGTCATCAAAAA	9873
rs369934177	snp	A/G	1.93646e-05	0.00311158	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73001053	AGAAATGAAGTTTTT[A/G]TAGTTTTCACATATA	9873
rs369941149	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72973913	CTATTTATTATCTGT[C/T]CCTTTACAAGAAATG	9873
rs369948122	in-del	-/A	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73074090	CAGTGTGATATCGGG[-/A]AAAAAATATTTCAAA	9873
rs369961395	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73069310	GCAAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	9873
rs369975719	snp	A/C/G	3.29491e-05	0.00405877	missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843247	CGGCCAGGGACTGCA[A/C/G]CATGCTCAGGAGGCT	9873
rs369985163	in-del	-/TG			intron-variant	FCHSD2	GRCh38.p7	11:72958994	CTCATCAGTAAGATA[-/TG]TGTGTGTGTGTGTGT	9873
rs370003615	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72886485	CTTCAACTATACTTA[A/G]TGCACCACTCCTCGG	9873
rs370014040	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73125024	GACCAACTCAGAATT[C/G]TATATCCAGCAAAAA	9873
rs370021960	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73029408	ACTCCCAGAGAAAGA[C/T]TTGGAGAGTAAATTA	9873
rs370022558	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73043069	TTGACTGATGCTCTG[G/T]CTAGAACTTCTGCCA	9873
rs370065778	snp	C/T	0.000131898	0.00811982	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842612	TCAACTGTCTCCCCT[C/T]TCAGGTACCTGAATC	9873
rs370068827	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72875394	ATTTGACAGAGTCTC[A/G]CTCTGCTGCCCAGGC	9873
rs370091016	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005993	GCTTACTACAGCCTC[A/G]AACCCCTGGACTCAA	9873
rs370098964	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73098394	CTAGCTTCATTCCTC[C/T]ATGGGTAAAGAAAAT	9873
rs370113610	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72888603	AGTCTTCGAGATATA[C/T]TTTCTTTCTTTCTTT	9873
rs370119525	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72861754	GACCGACATAGAGAA[A/C]CCCTATCTCTACTAA	9873
rs370143460	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72956602	GTGTCTGGTGAGGGC[C/T]CACTTCCTGGATCAT	9873
rs370152940	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73089196	ATAATCTCCATGTAA[C/G]ATGAAAAGGCATTTG	9873
rs370154472	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73118757	CTTACCACGTGTAAT[A/G]CATTGTTCTGAATGC	9873
rs370191845	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72936878	TCTTTGAAATATATT[A/T]AAAATAGGCGATTTA	9873
rs370218294	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943440	AAGGATTAGTGAGAC[A/G]CTGAATCAGGAAAAA	9873
rs370218807	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73001961	CTAGCATGCTCCTAC[A/G]CTATTTATAAACACA	9873
rs370226557	snp	A/G	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:72909841	CTCTGCCCGGCAGCC[A/G]CCCCATCTGGGAAGT	9873
rs370246364	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73088289	TACAGTAACATGTTG[C/T]ACAGGTTTGTAGCCT	9873
rs370251087	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73076454	AAGAAAGGAGACATA[C/G]CATATGATTACATTT	9873
rs370251322	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72977479	TAAGGAGCTCAAACA[A/G]CTCTATAGGAAAAAA	9873
rs370262297	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73128534	AATTTCTGGTAAAAA[-/A]TTTCTTCCCTGGTGG	9873
rs370271176	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73067312	TAGGGAGGGGAATAT[A/C]ACACACCAGGGCCTG	9873
rs370273285	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72934224	TCTGTATCTTGTCTA[G/T]CATTTTACATTTAAA	9873
rs370276042	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72881626	CAGTGGCCAAGATGT[A/G]GAATCAACCTAAGTG	9873
rs370292311	in-del	-/ACACACACACAC			intron-variant	FCHSD2	GRCh38.p7	11:73051869	TAACACGGTATATAA[-/ACACACACACAC]ACACACACACACACA	9873
rs370292718	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142046	CGGGCGGCAGGCGGA[C/T]CCCAGCCAGAGAGCG	9873
rs370311064	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73013288	GGGTTATTTTCACTT[A/C]GAATTTCTTTTACCA	9873
rs370324130	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72896399	TCCCATCCCAGCTTC[A/G]CTTTGTCCTTTTTCA	9873
rs370333227	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72992816	AACCCTAGAAGAAAA[C/G]CTAGGCAATACCATT	9873
rs370339159	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73054969	CATACTTGAGACTGG[A/G]TAGTTTATAAAAAGA	9873
rs370342500	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72948370	ACTTCAAAATTACTG[A/G]ATGTTTCATTTTTCA	9873
rs370345537	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73038660	TTGAATACAAATGGA[C/G]ATAAACATGGGAATA	9873
rs370352416	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72916027	ATTATGAGAACACAT[A/G]GGAACAACGCACACT	9873
rs370353231	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73082075	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	9873
rs370357373	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72866472	ACAGCGTTTCACCAT[C/G]TTGGCCAGGCTGGTC	9873
rs370364523	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73093466	GTATTAGGGATTCTC[A/G]AACTTACAGCTGGTG	9873
rs370375451	snp	C/T	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:72976416	CCCACTTCAGCCTCC[C/T]GAGTAGCTGGGACTA	9873
rs370380429	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73022579	ATACTAATGAAAGAA[A/G]GAAAAGAATAAAAGA	9873
rs370381174	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72852237	ACAGATGCTGGTGAC[A/G]TTATGGAAAAAAGGG	9873
rs370382406	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986683	TTGCATGTAGATCTT[A/C]CAATATAAGGTTTTA	9873
rs370402231	in-del	-/GT			intron-variant	FCHSD2	GRCh38.p7	11:73081783	AAGGGCATCATAACT[-/GT]TGCTATTTCACAGGT	9873
rs370413143	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72857282	TGTTACACTGTTTTC[C/T]TGACCCAGCATTTCT	9873
rs370426539	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73097017	TTTTTTTTTTTTTTT[G/T]ATGAGACAGGGTCTC	9873
rs370437908	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987319	TTTCATTTATCATTA[C/G]GCAAAATTAACCTCT	9873
rs370473294	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72967337	TAGGCTGGTAACAGC[C/T]GAAAAGTGGAAACAA	9873
rs370485215	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72903928	TATTGAGAGAGTTTA[C/T]CAGGTCCAACATGAA	9873
rs370490694	in-del	-/GTTTT			intron-variant	FCHSD2	GRCh38.p7	11:72892609	GTTTTTGTTTGTTTT[-/GTTTT]TTGTTTTTTGAGACA	9873
rs370494051	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72874102	CTCAAATAAAAAAAA[-/A]TTTAATGTGCCTAAG	9873
rs370517191	in-del	-/TATG/TATGTATG	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73025992	TATAGAGATTCATTT[-/TATG/TATGTATG]TATGTATGTATGTAT	9873
rs370564816	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72861215	GTGATATCTCTACTA[A/G]TTTTCCAGATAATCA	9873
rs370567817	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72995082	GAATCAAATAATATG[C/T]GGCCTTATGTTTCTC	9873
rs370570752	in-del	-/CAAAGAC			intron-variant	FCHSD2	GRCh38.p7	11:73084936	CACCAGTGCAAAGAC[-/CAAAGAC]ATAAGAGTAAGAAGG	9873
rs370571733	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72959813	GCTGATGAGCAGAGG[C/T]AGAACTATACTTCAA	9873
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	9873
rs370577358	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72881132	AATTATTCATGCAAC[A/T]AGGGACTAATATACG	9873
rs370584105	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73120899	AGCACTGGATGTTAT[A/G]GGAACACACAGGCAG	9873
rs370588594	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73036378	ACAATATTTCACAAC[A/G]TTATATCGGTCTTTG	9873
rs370592445	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73137922	AGTGTTTGACCTTTA[C/T]CCAGAAGGCCACAGA	9873
rs370594630	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081305	AGGGCATGGTGGCAC[A/G]CACCTGTAGTCCCAG	9873
rs370601705	in-del	-/TA			intron-variant	FCHSD2	GRCh38.p7	11:72980675	GTATGTGTGTGTGTG[-/TA]TATATATATATATAT	9873
rs370604763	in-del	-/TA			intron-variant	FCHSD2	GRCh38.p7	11:73107036	TTTTGTTAGAAAAGC[-/TA]TATATATATATATAT	9873
rs370615702	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73053329	CTATTCATTGAGAGA[C/T]AATTTAAATTTAACT	9873
rs370616838	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72922890	TTCCATTATCTAATT[C/T]CAGAACATTTCCACC	9873
rs370633105	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73080296	GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	9873
rs370643448	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73021882	TCACTTGAGCCCAGG[A/C]AACACAAGGAGACCC	9873
rs370661533	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953672	TAAATGTTATGGCAG[G/T]TTGTAATAAATACAA	9873
rs370681950	snp	A/C/T			intron-variant	FCHSD2	GRCh38.p7	11:72999398	GATCTCAGCTCACTG[A/C/T]AATCTCCACCTCCCG	9873
rs370687106	snp	C/T	3.31175e-05	0.00406911	intron-variant	FCHSD2	GRCh38.p7	11:72984263	AAACTGATATTGTAC[C/T]GCAAAACACATAGGA	9873
rs370689006	snp	A/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73109152	TGAAGTCAGGTAATG[A/T]GATTCCTCCAATTTT	9873
rs370691571	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73088779	ATGAACTAGTTCACA[C/T]TTTCACCATTTAAAA	9873
rs370700420	in-del	-/CCTATTGT	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:73099090	AGGTAGTGGTACATG[-/CCTATTGT]CCCAGCTACTCAGGA	9873
rs370701482	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044911	CCATCTCTACTAAAA[A/T]TACAAAAAATTAGCC	9873
rs370751936	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73026856	ACTTCCCCCTTTGCT[C/T]GCTCTCTCTCCTGCG	9873
rs370759240	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73037636	TTTCCTAAAAACTTA[A/G]GGCCCATACTGATTA	9873
rs370799159	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72867128	CTGTAATAAATACCA[C/T]TGAGGAAATAAACAG	9873
rs370817258	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73078858	AAGTAGTTACGACTA[A/G]AGGCATGCGTCACCT	9873
rs370830651	snp	A/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836574	AGGATATTACACCTA[A/G]CACATGGGGGCTTCA	9873
rs370859529	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889268	GCCCGGCTATAATTA[C/T]GTCTTTTAAAAAATA	9873
rs370861205	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72994371	TTAGTCCTTGAAACG[A/G]CTCTATGAAAAAGGT	9873
rs370871782	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72954074	CACTTTGGCTATTAC[A/G]CAGAGAATAGACATA	9873
rs370899725	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72873381	TATGGGTCATTCATA[A/C]ATCTTCTTTGGAGAA	9873
rs370908059	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73112656	TTGTTGGTGGTGGTG[G/T]TGGTGTTGTTGAGAC	9873
rs370915712	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72913825	AACCAAAAAAAACCC[-/A]AAAAAAAAACAAAAA	9873
rs370915900	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73084187	TGGACTTAACCAATG[G/T]AAGAGGGAACTAATG	9873
rs370925163	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73097508	ACATTCCCTTTTCTT[C/T]TGTTTTTTTGGAATA	9873
rs370929444	snp	A/G	0.000153988	0.00877327	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841004	TACTTGAGTTGTTGA[A/G]CAATAATGCTGATGC	9873
rs370930426	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73065180	AAATCAGCTTCATAC[C/T]TGGGATGTAAGGCTG	9873
rs370979720	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73057015	GTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC	9873
rs370995018	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110317	GCAAAGCCATTAGGT[A/C]TTGGACTTGGCTTTG	9873
rs371020243	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72980343	ATGAATCTGCTCCGT[C/T]GAAACTTTTCTTCAG	9873
rs371024327	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73070383	GAACCTAGCATCACG[C/T]CAGTCGTAAAGTAGA	9873
rs371074155	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72917396	CAAATCAATTGACCA[C/T]AGATGTTCAGGTTTA	9873
rs371076366	in-del	-/G			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140782	CCACTTCAAACAGCG[-/G]AGAACAGCAAATGCC	9873
rs371134360	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72999315	ATCTTACCAAAGATT[-/C]TTTTTTTTTTTTTTT	9873
rs371136794	in-del	-/GTTGTTGTT			intron-variant	FCHSD2	GRCh38.p7	11:72961426	GTTGTTGTTGTTGTT[-/GTTGTTGTT]TTTAATAGATGGGGT	9873
rs371168620	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72977895	ACTATTCAAAATAGC[A/G]AAGACTTGGAACCAA	9873
rs371204300	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73082802	CCCCACATATAAAGT[A/C]ATTGCTTAAAGGGTC	9873
rs371210131	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72954822	AGGCTACAAAGAATC[C/T]TGAAGTATTGAACCT	9873
rs371222056	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72945338	TGCTGGGAATACTGG[C/T]TAGCCATATGTAGAA	9873
rs371235112	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73121843	GAGTTCCTGATGCAG[A/G]AGATTAGGGATAAGC	9873
rs371242867	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73091472	GAGAATCACTTGAAC[A/C]CGGGAGGCAGAGGTT	9873
rs371254431	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73058243	AATCAGCCAGGCTGA[C/T]GCTACAGCAACCTGG	9873
rs371260996	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73024923	CATTAGAAAAATGCA[A/T]ATCAAAATCACAATG	9873
rs371262804	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72914281	TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT	9873
rs371268181	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73034672	ACTACATCGCCTACA[C/T]TGTTGAAGTTTCCCA	9873
rs371277740	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72890015	TACTGCTTTGTAGAT[A/G]GATCAGAAGGCCTTC	9873
rs371282008	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73004440	CCTGATTCTACTCAA[A/T]CCCTTTAGAATTCTG	9873
rs371294708	snp	C/T	0.000153988	0.00877327	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72989048	CCTTTAGCTAAATCT[C/T]TCACTGTCTCTTGTA	9873
rs371306830	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73038178	GAGATCTGTCTCTAT[G/T]AAAAAATTTAAAAAT	9873
rs371311109	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73103661	TGTAAAACCTACACA[A/T]AAAATACAGATATTA	9873
rs371313184	snp	A/T	1.8592e-05	0.00304888	intron-variant	FCHSD2	GRCh38.p7	11:73001147	CTCCTAAATTCAAAG[A/T]GGGATAGAAAAGCAT	9873
rs371330272	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72992047	CTCCTTAAGCTGATA[A/G]GCAACTTCAGCAAAG	9873
rs371332699	snp	A/C	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72950933	CTAATTCAGTGTGAA[A/C]AGAAGTAACATTTGC	9873
rs371339065	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120521	GATCACCTGAGGTCA[C/G]GGGTTCGAGACCAGC	9873
rs371381983	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72918132	TGGTTAAGTTTATTC[C/T]TAGATAGTTTATTCT	9873
rs371394729	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73025023	CGTGGAGAAAAAGAA[C/T]GCTTATACACTGTTT	9873
rs371403865	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72937570	TAGATGTTTCCATCT[C/T]CTGACCTCATGATCT	9873
rs371405339	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72988227	CCTGAGTCTCAGCTC[A/T]CCTTCTCACAGATGT	9873
rs371420183	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73101901	GAATATATTGTGTCT[-/A]TGTATGAAAACAGAT	9873
rs371424307	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73012161	ACAAAAGTATAGTTC[A/G]TCAATACTATGGCAC	9873
rs371437419	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73068759	AGGACTGCTTGAGCC[C/T]AGGAGTTCAAAACCA	9873
rs371444969	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73051671	AGAGATGTACTGGCT[A/G]TGCAACAATAAAACC	9873
rs371448419	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73127699	CATCAATTATTAAGG[C/G]GCAAATTATTCAGCT	9873
rs371486749	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123874	ACTATAAATCAAAAC[A/T]AGGTGGTCAAACTGA	9873
rs371551490	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72965098	CTGGCCAATCATTTT[A/C]CTTCTTAATTCAAAG	9873
rs371566450	snp	A/G	5.52257e-05	0.0052545	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902573	AGGCTGGAACTGGAA[A/G]GGCTGGGGTTTGTGA	9873
rs371582743	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73058963	TTCCACAGTCCTTAC[A/G]TTGATAGGCTAGCCT	9873
rs371632308	in-del	-/GG			intron-variant	FCHSD2	GRCh38.p7	11:73114851	TCTCAAGCGGAAGGA[-/GG]GGGGGTCTTTTTTGA	9873
rs371645598	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72863614	TCTGATAAAGGATTT[C/G]TATTCAGAGTATAAA	9873
rs371655675	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72917802	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	9873
rs371674049	snp	A/C/G	4.94224e-05	0.00497083	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843269	CAGGAGGCTGTTCGA[A/C/G]GTGGGAAACTGTAGG	9873
rs371713208	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72974158	TAATTATAAACAACA[G/T]ACGTTTATTTGGTTC	9873
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	9873
rs371758125	snp	A/T	3.49583e-05	0.00418066	intron-variant	FCHSD2	GRCh38.p7	11:73000980	ATAAGAACAGAAATA[A/T]AAACAATACCCTTTT	9873
rs371765543	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73129359	ACAGGAGGTGAGTGG[C/T]GGGCAAGCAGGCCAA	9873
rs371785507	in-del	A/GAT			intron-variant	FCHSD2	GRCh38.p7	11:72940405	AATATTAAAGGAAAT[A/GAT]ATATATGTAATGAGG	9873
rs371791504	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73060247	AAACAAATGTCTAAT[C/T]GTACCATATTTTGGC	9873
rs371799308	snp	A/C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73001523	TAATAAGGTAACTGA[A/C/G]GCCCAGAGAGATTTT	9873
rs371819619	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73110678	ATTTATTTCTGCTCC[A/G]ATCTTTATTATTTCT	9873
rs371820427	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72912238	AATCTTAGAGGAAAC[A/G]CATTCAGTTTTTCTC	9873
rs371827007	snp	A/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72971820	CTACAGAACTGTGAG[A/G]TAATAAATGGAGGTA	9873
rs371845004	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72980399	TTATCCAGTTATGGG[C/G]GCTCATCAGAGTTAC	9873
rs371869960	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72860703	TACAAAATTTAGCTG[A/G]GCGTGGTGGTGCTGG	9873
rs371886568	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943934	TTTAATCATTATTCA[C/T]TGTGATGCTGCCAAC	9873
rs371901947	in-del	-/ATTT			intron-variant	FCHSD2	GRCh38.p7	11:72850385	CAGAGATTTTTTTTT[-/ATTT]TATTTTTGAGACGGA	9873
rs371922660	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73068481	GTAACAAACCTGCAC[A/G]TCTTGCATATATACT	9873
rs371969922	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73026827	CATGAGATCTAATGG[C/T]TTAAAAGTTTGGCAC	9873
rs371995664	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72971259	AATGTTACAGTAACA[C/T]TGAGAAATATGAAAT	9873
rs372015593	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72905834	TTCTTAATCCAGTCT[A/G]TCATTGATGGACATT	9873
rs372047817	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72862017	ATATCTGAATAATCA[C/T]CAATGCAATTACACC	9873
rs372054931	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72944301	CAACGACAAAAACCA[C/T]ATGATTATCTCAATA	9873
rs372109238	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72913833	AAACCCAAAAAAAAA[-/C]ACAAAAAAAAAAACC	9873
rs372120877	snp	C/T			synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72849773	GTAGGAATAAACAAC[C/T]TTGCAGGTGAGTGGA	9873
rs372155918	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72997989	TGAACTACCACTCCC[A/G]TCCCCAAAAGATGAG	9873
rs372160233	in-del	-/CCCAAT			intron-variant	FCHSD2	GRCh38.p7	11:72863659	TAAAAATAAAACAAA[-/CCCAAT]AAAAATTAAACAAAG	9873
rs372170666	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73113521	CTACAAGCATGTGCC[A/C]CCACGCCCAGCTAGT	9873
rs372183073	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73050106	TTGGCTCTGCAGGCC[A/G]TAAGATCTCCAGGGC	9873
rs372187815	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083129	TAAATCAACAAACTT[C/G]TAAAAAGTATTATTA	9873
rs372206901	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73103463	TCAGAAATCATTACC[C/T]GAATCCCTAGGGTGA	9873
rs372250808	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72981679	CTATGTAATACCTAA[C/T]ACGATACTAAAACCA	9873
rs372258795	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838754	AAACTCCAAGCCTGG[C/T]CTTGATTGTAGCAGT	9873
rs372271675	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73048323	ATCTCCCTTAAGCCA[A/C]GGTTCATGATAGTCT	9873
rs372280505	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73003573	CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG	9873
rs372280601	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72969862	GGTTATGCTAGGTAC[A/T]ACACGACCAAATACA	9873
rs372284799	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73131307	TGGATCACAAGGTCA[A/G]GAGATCGAGACCATC	9873
rs372287081	snp	A/G	0.000149314	0.00863915	intron-variant	FCHSD2	GRCh38.p7	11:72887603	TGGGACAATAATGAT[A/G]ACTGTTTTTTACTTT	9873
rs372299821	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73093977	ATACTTTGGAAGGCC[A/G]AGTCAGGCGGACAAC	9873
rs372301561	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73121553	TCTTGGGTTGCTAAG[A/C]TTTAAATGAAATAAT	9873
rs372311035	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72930684	GGGAGGGAGGCTACA[-/A]GTAAGCCAAAATCGT	9873
rs372311189	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72910488	GTAATAAGAAAAATT[A/C]TTCTGCCTTGGGATG	9873
rs372311715	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114612	AGGTATTGCTGCTGG[C/T]TCCTCAGGGCCCAAG	9873
rs372313536	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73029257	CTTACAAGACTATTG[C/T]AGGAGCAAATTCTGA	9873
rs372332271	snp	A/G	0.000153988	0.00877327	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840975	CTAAGGGAGAAAACC[A/G]AAGAAGCTCATTTTA	9873
rs372366696	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73034027	CCGATAGCAAATATA[A/T]CATCTTTTTTTAAGA	9873
rs372391210	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72963328	AGTGAGCATTTACTA[C/T]GCACTATCTCATTTA	9873
rs372401086	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72878587	CAAGGACTAACGGGG[A/G]TAATGTCAAAAGTAC	9873
rs372425489	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72862710	TCCTGATAGGCTTTT[C/T]GGGGTAGAAAACCAA	9873
rs372436241	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72992327	AATATCGTGAAAATG[A/G]CCATACTGCCCAAGG	9873
rs372441212	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840359	AATTGCAAAGTATCC[A/G]ACTGGATTACCGTGC	9873
rs372465008	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73039315	TTGAGGTCAGGAGTT[A/G]GAGACCAGCCTAGAC	9873
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	9873
rs372521605	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72895221	CTGAGCCTTGGGACA[A/G]TTCTGGAAAACTCTG	9873
rs372565576	snp	G/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73131274	TGTAATCCCAGCACT[G/T]TGGGAGGCCGAGGCA	9873
rs372572079	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73101621	TTTGTATTTTTTGTA[C/G]AGACAGGATCTTACT	9873
rs372573511	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72850427	CTGTTGCCAGGCTTG[A/G]GTGTAGTGGCGTGAT	9873
rs372581330	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73069428	AACTGAAAAAAAACT[G/T]GTATAAGAACATATA	9873
rs372620540	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72902378	TGAGTTTCTTGGCCA[C/T]AATTCAGAAAAAAAA	9873
rs372620576	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72878933	CCAACATGGTGAAAC[C/T]CCGTCTCTACTAAAA	9873
rs372631550	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72966719	TCATGAAGTTTATAG[C/T]ACACTAAAGGTAGGA	9873
rs372641793	in-del	-/A	0.24019	0.249807	intron-variant	FCHSD2	GRCh38.p7	11:73077097	CTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	9873
rs372658067	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73013739	TTGCAATACTTTTTT[-/T]AAATTAGGGTTTATA	9873
rs372669164	in-del	-/AGA			intron-variant	FCHSD2	GRCh38.p7	11:72935220	CTTGTTTGAAGAAGA[-/AGA]TTATGATGAATTAGG	9873
rs372678020	in-del	-/AGTA	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72980612	CCACAGTCCTCCAGC[-/AGTA]AGTGATTTCCATCAC	9873
rs372685355	snp	A/G/T	0.000165551	0.00909679	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841611	GAAGCGAGGTTACCC[A/G/T]GTGCTCCCCTCCAGG	9873
rs372687487	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73078999	GTTGGGATTACAGGC[A/G]TGCGCTACCGCACCT	9873
rs372687874	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73102494	GCAATGAAACGAAAC[A/G]TCCATCAACTGATGA	9873
rs372694728	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73035784	GGAGTACAGTGGCGC[A/G]ATCTTGGCTCACTGC	9873
rs372699005	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73043968	ATTCACCAATTTTGG[C/T]AACAAACTATTAGGT	9873
rs372733176	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72947725	GTGATAAAATCATTA[G/T]TTAAAAAAAATATTG	9873
rs372765515	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73123341	ATCCCTGAGGTCAGG[A/G]AAAGTATCTGAAATG	9873
rs372779512	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73097615	TTCTTGTGAGGTGTT[-/C]TTTTTTTTTTTTTTT	9873
rs372805734	in-del	-/GTTC			intron-variant	FCHSD2	GRCh38.p7	11:72873444	TGAGTATTTTTGCCT[-/GTTC]TTTTATTATTATGAG	9873
rs372808884	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72937521	CATGTCATGGACATA[C/T]GGGACCATTAATGGA	9873
rs372841337	snp	A/G	0.000153988	0.00877327	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843400	ACAAAGACCAAAACA[A/G]ACTCCTAAAAATGTC	9873
rs372850671	snp	C/T	0.000241687	0.0109902	intron-variant	FCHSD2	GRCh38.p7	11:72921806	TTGGATAACACTACA[C/T]GTTGCACTAAAGGTA	9873
rs372852511	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72983074	CTGAGGCGGGCGGAT[A/C]ACGAGGTCAGGAGAT	9873
rs372858683	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73097546	TAGGATTGGTGTTAA[C/T]TCATCATTAACTGTT	9873
rs372895283	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73133855	AGTCGCAAGATTCCA[C/T]TTCTATAGAGACAGA	9873
rs372899478	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73085530	TTTCTCTTTTTCCCC[C/T]TTTGAGAGCCAGATC	9873
rs372903933	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73052223	GATTTCTAAACTGTA[C/T]AAATCTATGAAAAAT	9873
rs372905938	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892073	AAGAGAATGAATTTG[C/T]AGGGAGTAGCTAGAT	9873
rs372923584	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72953253	GTAGTGAGGTAAACT[A/C]CAGATCTTAGATCTC	9873
rs372925366	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72967136	ACCCGGGAGGCAGAG[C/T]TTGCAGTGAGCTGAG	9873
rs372930452	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73004630	TACCCTTGCCTCTTT[C/T]TCTTTCCACCTTTAT	9873
rs372934014	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73017210	GGCTCAACTCCTGGG[A/C]TCAAGCAAGCCACCT	9873
rs372934826	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73002723	TTCTCCTAGTTAATA[A/G]CTGTTTGCCCTTCCA	9873
rs372941463	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72984759	ACGAAATAGATTTTG[C/T]AGAGCTTTCCAAAGC	9873
rs372950360	snp	C/T	6.65059e-05	0.00576616	intron-variant	FCHSD2	GRCh38.p7	11:72849918	GAAACCATTGGCTAG[C/T]TTCCTTACTTCAAGA	9873
rs372956797	snp	C/T	4.25288e-05	0.00461114	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867983	ACAGAAACACCAATC[C/T]GCTTTAGCAGGTCCA	9873
rs372956857	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73066885	CTTACACTGTTGGTG[A/G]GAGTGTAAATTACTT	9873
rs372961576	in-del	-/ACACAC			intron-variant	FCHSD2	GRCh38.p7	11:73051869	TAACACGGTATATAA[-/ACACAC]ACACACACACACACA	9873
rs372970893	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72872063	AAACATTACATAAAA[C/T]TTACTATCTGCACCA	9873
rs372985899	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73097059	CCAAGCTGGAGTATA[A/G]TGGCACAATCTCAGC	9873
rs372987116	snp	A/G	0.0162398	0.0886349	intron-variant	FCHSD2	GRCh38.p7	11:73124689	TGAACCAAGGGGGCG[A/G]AGGTTGCAGTGAGCT	9873
rs372987922	snp	A/T	2.34277e-05	0.00342247	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72921879	CTGCACAGCTTGGCA[A/T]GTTTCTAGCTCAGTC	9873
rs372990461	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73023248	ACTACAAAGAGAATA[A/C]AAAGACAAGCTGCAG	9873
rs372990609	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72999590	CATCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC	9873
rs372996021	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72918213	TTCATTGATGGAATA[C/T]AGAGATGCAACTGAT	9873
rs372996239	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73009640	AATTTACTTCTCCTT[C/T]ATTTATGAAGGATAA	9873
rs373005159	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73068045	AACCATCAGATCTCG[C/T]GAGACTTATTCACTA	9873
rs373012061	snp	A/C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135071	GTTGGCCAGGCTGGT[A/C/G]TCGAACTCCTGACCT	9873
rs373024382	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72987826	TAAAAACGACTATGA[C/T]AGTATATTCCCAATG	9873
rs373037782	in-del	-/ACAC			intron-variant	FCHSD2	GRCh38.p7	11:73051868	TAACACGGTATATAA[-/ACAC]ACACACACACACACA	9873
rs373040966	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72909186	GGATTGCAGGCACAC[A/G]CCGCCACGCCTGACT	9873
rs373042591	snp	A/C	0.000153988	0.00877327	intron-variant	FCHSD2	GRCh38.p7	11:72921963	AGCCTGTAATAGAGG[A/C]GTAAATAAAAGAAAA	9873
rs373046545	snp	A/C/G			intron-variant	FCHSD2	GRCh38.p7	11:73107286	TCGATCTGACCTTGT[A/C/G]ATCTGCCCAGCTCGG	9873
rs373047862	snp	C/T	0.0228947	0.104514	intron-variant	FCHSD2	GRCh38.p7	11:72954443	ACTCCTGGGCTCAAG[C/T]GATCCTTCCCCTTCA	9873
rs373054301	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72886623	TCCATACCCCTTCAC[C/T]ACATTGCTGCTGAGT	9873
rs373075007	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72865587	CATTCCCTTCCTTCA[C/T]AACGAGAACAGCCCT	9873
rs373087879	snp	A/C	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72948371	CTTCAAAATTACTGA[A/C]TGTTTCATTTTTCAA	9873
rs373101435	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73003832	AAAAGTATCAGCCAG[C/T]GTGGTGGCTCAAGCC	9873
rs373133591	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72846013	ATGGGGTGTTTGATA[A/G]TATCTTCCTCATAGG	9873
rs373137786	snp	A/G	0.00152016	0.0275276	intron-variant	FCHSD2	GRCh38.p7	11:72984246	AATAAAATAATCAGT[A/G]CAAACTGATATTGTA	9873
rs373143205	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72851644	GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATTGC	9873
rs373171773	snp	C/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72945670	CAAAGGGCTAATATC[C/T]AGAATCTACAATGAA	9873
rs373184299	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73052947	CGCCTCCTAGGTTCA[A/G]GTGATTCTCCTGCCT	9873
rs373197019	snp	A/G	3.29935e-05	0.00406149	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843543	GAAGCCTGCAGTGTA[A/G]GATGGTCATGGACAA	9873
rs373226801	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73080044	AGCTCATGCCTCTAA[A/T]CCCCAGTGCTTTGAG	9873
rs373277761	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72924474	TTTTCAGTAGAGACG[A/G]GGTTTCACCGTGTTA	9873
rs373288395	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72914868	GCAATTGCAACAAAA[A/G]CAAAAATTGACAAAT	9873
rs373289650	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73055300	ATTAGCCATGATCAC[C/G]CCACTGGACTCCAGC	9873
rs373295551	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139109	TAGTGCCTAAATATA[A/G]GAGAGGAAAAAAGGA	9873
rs373334602	snp	C/T	2.18233e-05	0.00330321	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841433	AAATGCATTTAGACC[C/T]ATGCCCAGGAGAACC	9873
rs373338294	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963900	TTGGGGACCCTGGAT[G/T]AGATGACAACTCTGT	9873
rs373377265	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72873096	GCACTTCGGGAGGCT[A/G]AGGCGGGCAGATCAC	9873
rs373396483	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106374	TGGCACCACTACACT[C/T]CACCCTGGGTGACAG	9873
rs373406058	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73104702	GCCTCCCAAGTAGCT[A/G]GGACCACAGGCACGT	9873
rs373410364	snp	G/T	2.43028e-05	0.0034858	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72984090	AAAGCTGTATTACCT[G/T]CATAATGTTAACTAA	9873
rs373414387	snp	A/C	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73136440	GGAGTCTCAGCTACC[A/C]TGGAGGATGAGATGG	9873
rs373416543	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73065706	CATAAGCATTCCTAT[A/G]CATCAATAACAGACA	9873
rs373424848	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73087070	TTGTATCATAGGAGA[C/T]GACAGCTCCATGCAT	9873
rs373482789	snp	C/T			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72844035	CAAAAAAAGAGAGCA[C/T]TTCCTGGAAGTAGAG	9873
rs373483930	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72900829	TTTCTATTAAACTGA[C/T]ACCATTAAACTCTGG	9873
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	9873
rs373495264	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72925786	GGGTTGCACACTCCA[C/T]GGAGCCAGTGGCTAC	9873
rs373510520	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72866766	TTCTCATTAGAAAAT[C/T]AGAATGCTATGTGAA	9873
rs373522120	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73050793	CAGCAAATGAAAACT[A/G]TAATTAAGTTTTACC	9873
rs373525177	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72992839	ATACCATTCAGGACA[C/T]AGGCATAGGCAAGGA	9873
rs373530005	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72974092	GCGGGATGGAAGAAA[A/T]CAAAGTTTTGGTCCA	9873
rs373531357	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72907599	AGATAATCACGTGGG[-/TT]TTTTTTTTTTTTTTT	9873
rs373552324	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913427	GCATGTGCCACCACA[C/T]TTGGATAATTTTTGT	9873
rs373554640	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73120819	GCTCACAGTCTGGAG[A/G]TGAAGATATACCAAA	9873
rs373565219	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72992543	CAAAACAGCATGGTA[C/G]TGGTACCAAAACAGA	9873
rs373572752	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73077114	AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAAAAAG	9873
rs373572906	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72907567	AAATTTTGTTGAAGG[A/C]CTTTTCTGCATCTAT	9873
rs373579244	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72879626	TTTGAAATAAAAATT[C/T]ACAAGATGGCCTTAA	9873
rs373583526	snp	A/C	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73045753	AAGGGGAACATCACA[A/C]TCTGGGGACTGTTGT	9873
rs373590228	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72858594	CACATAGAGGGGATC[A/G]ACAGACACTGGGGCC	9873
rs373653514	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72983273	CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC	9873
rs373665021	multinucleotide-polymorphism	AA/TG			intron-variant	FCHSD2	GRCh38.p7	11:73030366	ATTATACTAAATAAA[AA/TG]AAACAAAAGGAGATA	9873
rs373666755	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72914765	CTTAAATGTAAAACC[C/T]GAAACTATAAAAACC	9873
rs373692654	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73031368	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGTGG	9873
rs373708559	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72992691	AAATGGTGCTGGGAA[A/T]ACTGGCTAGCCATAT	9873
rs373719529	in-del	-/TCTG	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73034867	AACCAAGACTGTCAA[-/TCTG]TCTGTCAACAACACA	9873
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	9873
rs373756132	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73118725	CTATAATGATGATGG[C/T]AAACACTAACTGAGC	9873
rs373764522	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038674	ACATAAACATGGGAA[C/T]AATAAACACTAGGGA	9873
rs373805762	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130106	GTCTCAATCTCCTGA[C/T]CTCGTGATCCGCCCG	9873
rs373842790	snp	C/T	0.000437904	0.0147905	intron-variant	FCHSD2	GRCh38.p7	11:73083677	TACCTAGAATGGGAC[C/T]TCCAATTTCAAGCTT	9873
rs373855802	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840093	ATGCTGCTCCAGCCT[C/T]CTAATCGCTCCCTAT	9873
rs373901992	snp	C/T	0.000542959	0.0164677	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867892	GCCATTACTGGTCAC[C/T]GCAGGAGGGCGGGCC	9873
rs373902675	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72915570	GCTCATGCCTGTAAC[C/T]CCAGCACTTTGGCCA	9873
rs373907491	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73043087	AGAACTTCTGCCACA[A/G]CGCTGAATAGGAGTG	9873
rs373921854	snp	C/T	0.00058987	0.0171635	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838893	AGCAGGAAACAATTA[C/T]GTAGTTTGTCAGTCA	9873
rs373926714	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73128707	ACTATCCAGCAATCA[C/T]GAGGAGAATCATTAC	9873
rs373946798	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72896643	ACTTTTAGTGATCAA[G/T]CCAATAAGGGAGTTG	9873
rs373949133	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73121568	ATTTAAATGAAATAA[C/T]AGATGTTTAACATTT	9873
rs373949284	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73067210	GAAGCTGGAAACCAT[C/G]ATTCTCAGCAAACTA	9873
rs373949897	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73036576	CCCTGATAAATTATA[A/G]TCATGATTACTGTGA	9873
rs373952785	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73110339	TTGGCTTTGCTAGGC[A/G]ATATTTTATTACGGC	9873
rs373954970	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72943077	GCTCACTACAACCTC[C/T]GCCTCCCGGGTTCAA	9873
rs373955787	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72887911	CATTAAGTTTGAGGT[A/G]GTTTGTTAAGCAACA	9873
rs373969244	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72930398	CCCAAAATGCAATTC[C/T]TGTTTTCCAAATAAA	9873
rs373976094	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73011515	TCTTGTGGTTTAGCC[C/G]TAGTGATGCTGGACC	9873
rs374005398	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72995937	GTAGACTTAAGGGTA[A/G]TGTCCAAACCCAGTT	9873
rs374006179	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72894754	GGTAAGTTTGGAGCC[A/T]AAACTCACTTGAGCC	9873
rs374025849	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73032003	GAACTATTAACTAAA[C/T]TATGGTCATCAGTAT	9873
rs374044633	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72923233	ATGCTGCAAAGTTAA[A/T]AAATAAATAAATAAT	9873
rs374049137	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73088888	AAATTATGTATTTTT[G/T]ACCCTTTTAAGTTTA	9873
rs374051157	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72893250	CAAGTGATCCACCTG[C/T]TCTTGGCCTCCCAAA	9873
rs374051654	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73128333	AACTGGAAATGGGTC[C/T]CTGCAGCAAATCAGG	9873
rs374054070	in-del	-/AA	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72852206	GAATGGCTATTATTT[-/AA]AAAGTCAAAAAATAA	9873
rs374054551	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73070466	TCTCGTTCTGTCGCC[C/T]AGGCTGGAGTGCAGT	9873
rs374057481	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72950704	TTTCCTTATTTCTTT[C/T]AGGATATTTTAATTT	9873
rs374057500	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73045051	CTCCAGCCTGGGCGA[C/T]AGAGCAAGACTCCAT	9873
rs374067751	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72874948	CTTTAAAGAGACAGA[A/G]CTTTTAAAAATAGTA	9873
rs374080134	in-del	-/TTT			intron-variant	FCHSD2	GRCh38.p7	11:72954197	CAGTAGATGTGGGGA[-/TTT]TTTTTTTTTTTTTTT	9873
rs374084325	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72917608	TTCGAAGACTGGGCC[A/G]AGTGCAGTGGCTGAC	9873
rs374092549	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72933638	GTAAGGAAAAAAAGT[C/T]GATTCACATGGACAA	9873
rs374093062	snp	A/C	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72890473	ATCAACTTGCCACCA[A/C]ACCTCAAAAGCCAGC	9873
rs374100201	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72860850	AATTAGAAAATATTT[C/T]GAACTGGATAAAAAT	9873
rs374125531	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72934491	GCATACCACCATACC[C/T]GGGTAATTTTTGTAT	9873
rs374142987	snp	A/C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911747	TAGTTACATATGTTC[A/C/G]CTTTTGTTGCCTAGG	9873
rs374145363	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72959708	CCCAATAGCTTTCTA[C/T]GTGTTTACTGAAAGG	9873
rs374192684	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853822	TTTGCAAGTTATGTA[C/T]CTTAAAAGGGACTAA	9873
rs374195299	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72927853	TAGATGGATCAGCAG[C/T]TGTTTTCAACGGGGA	9873
rs374234294	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:73132486	CTACCTTCAAAGCTC[-/TT]GTTTCCATTACCAGT	9873
rs374276600	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72865963	GAGACCAAGTTTTGT[C/T]CATCTTCAGTTTGCC	9873
rs374321817	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72910810	CCGAGAAACACCCAA[A/G]AATGATCAATAAATA	9873
rs374321963	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73031481	GTCTCCGAAAAAAAA[-/A]GAGAGACAGAGAGAG	9873
rs374334004	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72999413	CAATCTCCACCTCCC[A/G]GGTTCAAGCAATTCT	9873
rs374368422	in-del	-/CT			intron-variant	FCHSD2	GRCh38.p7	11:73113214	TTCTGAAGTCCTTCT[-/CT]GTGTTATCTCGAATT	9873
rs374372834	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73031110	TGTTAAGTGAAATAA[A/G]CCAGATAGAAAGAAG	9873
rs374388715	snp	A/G	0.000153988	0.00877327	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840854	ACTATGCATTCGATA[A/G]TCCTGCAAGATCAGA	9873
rs374410891	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73006006	TCGAACCCCTGGACT[C/G]AAGTGGTCCTCCCGC	9873
rs374415879	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72859647	TCCCCCACAGATAAG[C/G]GGGGACTGTAATGAA	9873
rs374427786	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73074375	TGTGCAAGCATATGT[C/G]CAAGCATAAAATATG	9873
rs374432808	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005330	ACCACTCTTCTGAAA[C/T]TGCTTGCCAAAGTCA	9873
rs374486468	in-del	-/A	0.00952359	0.0683454	intron-variant	FCHSD2	GRCh38.p7	11:72897337	AAAAAAAAAAAAAAA[-/A]GGATAGTTGTGTCTG	9873
rs374494257	in-del	-/CA			intron-variant	FCHSD2	GRCh38.p7	11:72954892	ACACACACACACACA[-/CA]GATATATACAGAAAC	9873
rs374496379	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72924456	CTTTTTTTTTTTTTT[G/T]TATTTTCAGTAGAGA	9873
rs374517176	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73119932	TTACAAAAGAAAGAA[G/T]TTTAATTGGACTTAC	9873
rs374519488	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106224	ACCAGCCTGGGAACA[C/T]AGTGAGAACCCATCT	9873
rs374522181	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72862228	GGCAAGGATTTCTGT[C/T]GACTCTCACCACTTC	9873
rs374530016	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73094207	CAGAGCAAGACTCTT[A/G]TCTCCCTGCACCAAA	9873
rs374530499	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889436	TCCAACATGAGTAGA[C/G/T]AGCTGACAGCACACT	9873
rs374532248	in-del	CTTTC/T			intron-variant	FCHSD2	GRCh38.p7	11:72912145	GCTCTTTCTTTCTTT[CTTTC/T]GTCTGACTGCTGTAG	9873
rs374537477	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73062166	TGATACCCAGGCAAA[C/T]AGGGTCAGGAGTGGA	9873
rs374539465	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093387	CACAAAATTGCAAGT[C/T]GTGTCAGAAGTAAAG	9873
rs374557443	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73032794	CTTCAAGAAACTTCA[C/T]ACAAGCTGGCATGGA	9873
rs374563514	snp	C/T			synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72889829	TTCTCTTACACTTAC[C/T]CGTTGTTGGTGAACA	9873
rs374569447	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73025545	AACTAATGGGTACTA[G/T]GCTTAATACCTGGGT	9873
rs374571969	in-del	-/CT			intron-variant	FCHSD2	GRCh38.p7	11:72896763	ATTAGGGGGAAAATA[-/CT]AAAAAAAAAAAAAAA	9873
rs374572551	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998701	GGAGGAAAAAATTGA[C/T]AATAAAAAATATTAG	9873
rs374576330	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72933133	CCTGATCTCAGGGGT[A/G]AACTTGCAGGGTAGG	9873
rs374587260	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72949188	GCGTGGTGGCTCACG[C/T]CTGTAATCCCAGCAC	9873
rs374587409	in-del	-/A	0.0020032	0.0315846	intron-variant	FCHSD2	GRCh38.p7	11:73044832	TCCCAGTACTTTGGG[-/A]GGCCGAGGCAGGTGG	9873
rs374631580	in-del	-/CTTTA			intron-variant	FCHSD2	GRCh38.p7	11:73098411	TGGGTAAAGAAAATA[-/CTTTA]TATGATTTTGATCTT	9873
rs374643152	in-del	-/AC			intron-variant	FCHSD2	GRCh38.p7	11:73066875	TAGGAACGCTCTTAC[-/AC]TGTTGGTGGGAGTGT	9873
rs374653615	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72992163	AACTCCCATTCACAA[C/T]TGCTTCAAAGAGAAT	9873
rs374657135	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72907149	TTGGCTCTCTATTAC[G/T]GCTGGAATGCCTGTG	9873
rs374660835	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72878941	GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA	9873
rs374661276	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73083158	TATTCATACTTGTAA[A/C]TACTTTACAAATATA	9873
rs374663881	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72918874	TACCTTCAGAGTTAC[C/T]ATCCTAGAGAAAATA	9873
rs374677204	snp	A/G			upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142396	CACCACTCAGGCCGC[A/G]GGAATTTCCGGCCTC	9873
rs374683303	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058465	TTTGAATACTACTAG[C/T]ATAACACATGATAGA	9873
rs374688945	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73025024	GTGGAGAAAAAGAAC[A/G]CTTATACACTGTTTA	9873
rs374694171	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937038	CATTTAAATAGCAGA[C/T]TTCTGCTCATCAACC	9873
rs374707465	in-del	-/A	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73138499	CCTGAACTGCTTCTG[-/A]AAATGTATTACTTTC	9873
rs374737492	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72876635	CTTTAAAAGAACATA[C/T]ATTCTACTCATATGC	9873
rs374744169	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72916372	TACAGTACAGTAGTA[A/G]CATGATCATAGCCTG	9873
rs374746074	snp	C/G	1.69192e-05	0.00290849	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73015828	AATCATTCCGATCAT[C/G]AGCTTTTACTCCAGG	9873
rs374752473	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72889227	CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT	9873
rs374777469	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72861655	AAAGGATAGGCCGGG[C/T]GCGCTGGCTCATGCC	9873
rs374790939	snp	C/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:72907627	TTTTTTTTCTTGAGA[C/T]GGAGTCTGGCTTTGT	9873
rs374815420	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108610	TCTGTCGCCCAGGCC[A/G]GACTGCGGACTGCAG	9873
rs374821033	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73112171	CATTTCTTATAGGAC[A/C]GGTCTGGTGTTGATG	9873
rs374821525	snp	A/C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73027697	ATTTCAGAGATGTTC[A/C/G]CTGCACTCCCCGCCA	9873
rs374825143	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73029045	ATACAGCAATGAAAG[C/T]AGAAAGTTAGTCAAG	9873
rs374829444	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73043230	GAGGTATGTTCTTTC[C/T]ATGCCCAGTCTGTTG	9873
rs374865039	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72903823	GGATAATTGAGGAGA[C/T]GCAAAAAGTAGTAGG	9873
rs374868216	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72983065	TTTGGGAGGCTGAGG[C/G]GGGCGGATCACGAGG	9873
rs374876270	snp	A/G	2.01375e-05	0.00317307	intron-variant	FCHSD2	GRCh38.p7	11:72921810	ATAACACTACACGTT[A/G]CACTAAAGGTAACTT	9873
rs374881802	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72881345	AATCAGATATCATCT[C/T]ACCCCAGTTAGAATC	9873
rs374900099	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72846249	GCAGTGGTGCCATCT[C/T]GGCTCACTGCAACCT	9873
rs374906780	in-del	-/AGAA	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72954107	GGTAGGGGTGGGAGT[-/AGAA]AGCCAATTAGAAGAA	9873
rs374910065	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73115594	GAATAGGGAAGAGAG[A/T]AAACACGAGAGAGAA	9873
rs374911982	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72987376	TTTTCACATTACTAC[A/T]GCAAGTAAGTTATTA	9873
rs374946138	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72854494	TGGAGTGCAATGGTG[C/T]GATCATAGCTCATTG	9873
rs374946704	snp	C/T	4.94262e-05	0.00497098	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843324	TGGCCAACTTTATTT[C/T]GAGCCTGGGTAAAAG	9873
rs375006222	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73057823	TTCCCCTCAGTTCTT[-/G]AGGGATCTAAGAGGA	9873
rs375050705	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043980	TGGCAACAAACTATT[A/G]GGTGAGTGAGAAATA	9873
rs375077629	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971877	TTTGTTACATAGCAA[C/T]GGAAATCAAATATAA	9873
rs375091855	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73132215	ATAATTCATGAAACA[C/T]GATAACTTCCTTTTG	9873
rs375101155	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73049290	GGAAAAAATTAAAAC[A/G]TGACAGAAACTGTCT	9873
rs375114793	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72925588	ATTCAAGAAGGAATT[G/T]GTTGCCACGGTGTAT	9873
rs375183560	snp	C/T	3.42214e-05	0.00413637	intron-variant	FCHSD2	GRCh38.p7	11:72984067	GAAGTAAAATTACCA[C/T]AGATATGAAAGCTGT	9873
rs375211663	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73103477	CTGAATCCCTAGGGT[A/G]AACCAAATATCTGCC	9873
rs375234198	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73112022	TCTACTTAAGAATAA[C/T]TTATACATCACAATT	9873
rs375234960	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73110151	TCTGTAGTTTTCTTC[-/T]TTTTTTTTTTGATGT	9873
rs375255208	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72910153	GCCCGGCTGCCCCAT[A/C]TGGGAAGTGAGGAGC	9873
rs375264770	snp	G/T	0.0256215	0.110247	intron-variant	FCHSD2	GRCh38.p7	11:73066810	GCCAGTTAGAATGGC[G/T]ATCATTAAAAAGTCA	9873
rs375268428	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73104848	CAGGCCTGAGTCACC[A/G]TGCCTGGCCAACTTT	9873
rs375284836	snp	G/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73107222	ACCATACCCAGCTAA[G/T]TTTTGTATTTTTAGT	9873
rs375294254	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73039299	GAGGTGGGCGGATCA[C/T]TTGAGGTCAGGAGTT	9873
rs375295493	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73065007	CCCTAACTCCTTTCA[C/T]GAGGCCAGCATCATC	9873
rs375307992	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73096656	AAAAAGGTGCATCCT[C/T]GTGTTCTTCCTGAAC	9873
rs375368255	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72877212	TTTTAATGATTAGTG[C/T]TTGTTCTCCTGTGAT	9873
rs375373670	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72893195	TAGTAGAGATGGGGG[C/T]TTTGCTATGTTGGCC	9873
rs375376049	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73115371	TGTATTTTTAGCAGA[A/G]ATGGGGTTTCACTGT	9873
rs375393711	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72972547	CCCTTTTATCTGCTT[C/T]ATATATAAAGATTCC	9873
rs375406196	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73006432	GCCCTGGAATCATCA[C/T]TGATTCCTCATTTGT	9873
rs375411975	snp	C/T	9.77613e-05	0.00699079	intron-variant	FCHSD2	GRCh38.p7	11:72988934	CATTTATTTGCATAA[C/T]AATTTTCTCAGAAAT	9873
rs375435105	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73017817	ACTTAAATTTCCTAA[C/T]GTAAACAATCACAAA	9873
rs375464183	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72934110	AAGACACTGTCTCAG[-/A]AAAAAAAAAAAAAAA	9873
rs375476948	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72871179	TGCTGCTTTGCTCCA[A/C]CAGCCATGCCTCTGA	9873
rs375480927	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73131092	ATCACATCTAAAACA[C/T]CACTGAGGGCTGGGC	9873
rs375482336	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72845527	TGCAGCACTAGTTGT[C/T]CAATGTAAGCAGACA	9873
rs375488152	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73015171	ATTCTAAACAAACAT[A/G]TACTTTTAAGATATC	9873
rs375490957	snp	C/T	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72945428	GACTTAAATGTTAGA[C/T]CTAAAACCATAAAAA	9873
rs375518533	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72988316	TTGTCACTGCAAAAA[C/T]CTCTATTATATTGCT	9873
rs375537394	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73122365	TCTGCTGCAGCTGAA[C/T]GCACCCTGATAGCCC	9873
rs375543755	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72981681	ATGTAATACCTAATA[C/T]GATACTAAAACCAGC	9873
rs375550096	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73084312	CAATGTACAAGGCCA[C/G]TACAAATTGTGGTAT	9873
rs375595227	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098676	TAAACTGAGAAAGAA[A/C/T]AGTCTCTTCAACAAA	9873
rs375601859	in-del	-/GT			intron-variant	FCHSD2	GRCh38.p7	11:73133816	AAAAAAAAAAAAAAA[-/GT]AACCATTATGCCAAA	9873
rs375617608	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72978031	ATGGATGAAGCTGGA[A/C]ACCACCATTCTGAGC	9873
rs375628821	in-del	-/ATATTTAT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72903207	TATTTATTTATTTAT[-/ATATTTAT]TTATTTATTTATTTA	9873
rs375656465	in-del	-/TAA			intron-variant	FCHSD2	GRCh38.p7	11:72890391	AACAAAACAATATAA[-/TAA]CAGCAACACAATCTT	9873
rs375668527	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73040135	TAATGTTACACAAAG[A/G]CTGAGTTCATTTGTT	9873
rs375686070	in-del	-/AGT			intron-variant	FCHSD2	GRCh38.p7	11:72927487	TGTATGTAGGGGAAG[-/AGT]GGAGTGTAAGGGAAA	9873
rs375687642	snp	C/T	0.00018128	0.00951879	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72887473	CTGCCACCTTACCTC[C/T]GCTTTACGAATATTT	9873
rs375707210	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73033287	GCGAGATTCCGACTC[-/A]AAAAAAAAAAAAAAA	9873
rs375709248	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72890926	AAATTACCCAAAGAG[A/G]CTTTTAATATAGAAA	9873
rs375755254	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73078285	GGAAAACTGGCTGTA[C/T]CTACTAAAGTAGAAC	9873
rs375788859	in-del	-/GT/GTGT/GTGTGT	0.496778	0.0400063	intron-variant	FCHSD2	GRCh38.p7	11:72959853	TTTTAAGTTTCTAGG[-/GT/GTGT/GTGTGT]GTGTGTGTGTGTGTG	9873
rs375791768	snp	A/G/T	0.00239393	0.0345281	intron-variant	FCHSD2	GRCh38.p7	11:73124482	AATAATGGGCCAGGC[A/G/T]CAGTGGCTCACACCT	9873
rs375834190	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73128964	GCAACCTCCATCTCC[C/T]GGGTTCAAGCGATTC	9873
rs375839124	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72892140	GTTACTGAGCAGCAT[C/T]TTAGGAATAGGTAAA	9873
rs375843071	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73102006	CAGACCCAGATAAAA[C/T]CCAATGCTACAATTG	9873
rs375875859	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73015104	CTGCCTTGGCCTCCC[A/C]AAGTGCTGGGATTAC	9873
rs375890603	snp	C/T	0.0193772	0.0965046	intron-variant	FCHSD2	GRCh38.p7	11:73001598	GATACAAGACGAAGA[C/T]TGGGTACCTGTATAT	9873
rs375894869	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73045312	GGAACACTTTTACAC[C/T]GTTGGTGGGACTGTA	9873
rs375904291	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72929030	TTCCAGCTTCATCCA[C/T]GTCCCTACAAAGGAC	9873
rs375942657	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72956320	AACCACCATTTGGCA[-/A]CCATCATAAAGGTGG	9873
rs375954074	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72870731	CAGTGAAACCCTGTC[A/T]CTACTAAAAATACAA	9873
rs375957423	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840448	TGAGGAGAGGTAACT[C/T]TGCAATAATATATTC	9873
rs375976990	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73095751	GAGGAAGCTTTCCTG[C/T]TCATAGTTTGAAGAA	9873
rs375978223	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72858051	GTAAAATATTTAAAA[C/T]CCCTAACACATGTTT	9873
rs375999717	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72966104	TATAACTACCAGCGT[A/G]ATGGATACATCTACA	9873
rs376027855	in-del	-/A	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73108978	TTTCCAGCACCATTT[-/A]ATTGAAGAGACTGTC	9873
rs376037263	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73068961	TCGAGGCTGCAGTGA[A/G]TCATGACTTCGCCAC	9873
rs376047908	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72931496	TTCTGGCCAGGCATG[A/G]TGGCTCACGCCTGTA	9873
rs376055737	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73004434	ACACCTCCTGATTCT[-/A]CTCAAACCCTTTAGA	9873
rs376058381	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72872725	GTTGTTTCTATTTCT[C/T]GGCTATTATGAATAA	9873
rs376069834	snp	C/G	0.0232847	0.105357	intron-variant	FCHSD2	GRCh38.p7	11:73061839	TAAAACCCCCATCTC[C/G]CTGGGACAGAGCACT	9873
rs376083184	snp	A/G	0.000163987	0.00905354	intron-variant	FCHSD2	GRCh38.p7	11:72868049	ACCAAGAAAATGGTC[A/G]GAAATCAAGGCTTTT	9873
rs376089245	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72908178	TAACATAATGACCTC[C/T]AGTTTTATCTATGTT	9873
rs376098610	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72969487	CTTTGTCTTAATTTT[C/T]TGAGGGTAGAGAGTA	9873
rs376103014	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72935452	AGACTTTGGTAAAAG[C/T]CAAGGATATAAATAT	9873
rs376103099	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72976994	GCAGTGGCATGATCT[C/T]GGCACACTGTGACCT	9873
rs376131197	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73037341	TGCTGTACAGTCTAT[C/G]TGTCTGGACAAACAT	9873
rs376134705	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058986	GCTAGCCTCTATAAC[A/G]TAAGGTGAAATAGAC	9873
rs376148389	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73004441	CTGATTCTACTCAAA[C/T]CCTTTAGAATTCTGA	9873
rs376171133	snp	C/T	0.000407028	0.01426	intron-variant	FCHSD2	GRCh38.p7	11:72867816	ACTACAGAGTCAAAG[C/T]ATGCTTCAGTGAAAA	9873
rs376176748	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72903256	GAGTCTCGCTCTGTC[A/G]CCTGGGCTGGAGTAC	9873
rs376183252	in-del	-/GAAA			intron-variant	FCHSD2	GRCh38.p7	11:73125798	GAAAAAAGAAAGAAA[-/GAAA]ATGGAATACTAACAA	9873
rs376186984	snp	G/T	0.00017584	0.00937491	intron-variant	FCHSD2	GRCh38.p7	11:72889802	TGGCTTAAGGTGAAT[G/T]TAACTAGGACTTTCT	9873
rs376190842	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73014587	AGCTTCATTGCCACA[C/T]TCTTAAGAAATCATC	9873
rs376202576	in-del	-/GA			intron-variant	FCHSD2	GRCh38.p7	11:72885238	AGTGGAAACCAAGTG[-/GA]AGATTATTTTATGCT	9873
rs376204027	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73135124	CTCCCAAAGTGCTGG[G/T]ATCACAGGCATAAGC	9873
rs376225949	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72876627	TATGTGTACTTTAAA[-/A]GAACATATATTCTAC	9873
rs376230330	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850168	TCCCAGGTTCAAGAA[C/T]TCTCGTGCCTCAGTC	9873
rs376244623	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909526	AGGAGCCCCTCTGCC[C/T]GGCCGCCCTGTCTGG	9873
rs376254108	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72941029	GGGCTTGGAAAGGAC[C/T]GTATGTTCCACCATG	9873
rs376264013	snp	A/C/T			intron-variant	FCHSD2	GRCh38.p7	11:73097112	GGCTCAAGCAATCCT[A/C/T]CCACCTCAGCCTCCC	9873
rs376268111	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72917818	GCTTGAACCTGGGAG[A/G]TGGAGGTTGCAGTGA	9873
rs376276570	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73088501	TACTAAAATAGTAAT[G/T]AAAGTTTTCTCTGGG	9873
rs376277937	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72943509	ATGTGAACTTCATAT[C/T]ACCTTGGTTATTTAT	9873
rs376279878	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909880	CCTCTGCCCGGCAGC[C/T]GCCCCATCTGGGAAG	9873
rs376289743	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73068858	AAAAAATTAAAAAAA[A/C]AAAAAAATCAGCCAG	9873
rs376293661	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73124179	AAAACCAAACACCGC[A/G]TGTTCTCACTCATGG	9873
rs376310150	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72925327	TAGAAGTATATTACA[A/T]ATCAGGAATTATACA	9873
rs376321678	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73000136	TTGGCAAACGGAAAA[C/T]TGGGGGGTTTTTGGT	9873
rs376325787	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72965806	TAGAATCACACAGTA[C/T]GTCATCTCTTGTGAT	9873
rs376326430	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72932983	AAGTTAAAGGAGTAA[C/T]TGATTTCATAAAACT	9873
rs376337070	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085757	AGGGGAATCTGATTA[G/T]CAGAGTTACCACAAA	9873
rs376355033	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73017759	TCTTCTAACCACTCC[C/T]ATTCCTACTTGCTAA	9873
rs376370110	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73051091	GAGGCCAAGGTGGGA[C/G]GATCGCTTGAATCCA	9873
rs376380363	snp	G/T	7.46714e-05	0.00610984	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838909	GTAGTTTGTCAGTCA[G/T]TTCCTGACTCAGTAT	9873
rs376386856	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72907747	AGGCACCCGCCACCA[C/T]GCCTGGCTGCTAATT	9873
rs376390504	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72880226	CGAATCCATGTGCAA[C/T]TGCTATCAAAATCAA	9873
rs376390897	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72966563	CAAGCTCCCTGCAAA[C/G]AGACTGGTTTTTCAT	9873
rs376396139	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73003833	AAAGTATCAGCCAGC[A/G]TGGTGGCTCAAGCCT	9873
rs376398152	in-del	-/AA			intron-variant	FCHSD2	GRCh38.p7	11:72899735	GTAAGACCCTATCTT[-/AA]AAAAAAAAAAAAAAA	9873
rs376409633	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72866836	TCAGTTTCGCTAGCA[A/G]GCCTGCCTGATATCT	9873
rs376421601	in-del	-/AAAATAAAATAAAAT	0.0225401	0.10374	intron-variant	FCHSD2	GRCh38.p7	11:73080961	CTCAAAAAAACAACA[-/AAAATAAAATAAAAT]AAAATAAAATAAAGA	9873
rs376431604	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73071456	CAGCACCTTGAGAGG[C/T]CGAGGCGGGCAGATC	9873
rs376485432	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72873347	AAAAAAAAAAAATGA[A/C]TCTTTTCATGTGCTT	9873
rs376486887	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72872477	TGCAGTCTTGACAAT[C/G]ACTATTCTACTTTCT	9873
rs376508779	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137370	CACCAACAATCTCTG[C/T]CTTTACATATTATAT	9873
rs376515630	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72963945	TCACAGTTGAATAAC[A/C]ATGGCTAATTAATAG	9873
rs376521432	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73106230	CTGGGAACATAGTGA[C/G]AACCCATCTCTACAA	9873
rs376604544	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73018952	TAAGTCAAGATCTCA[C/G]AATTCAAATAACTCA	9873
rs376612008	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73094843	TAGCACTAAAATGAT[A/G]ACCTGAGAATACAAA	9873
rs376635765	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73120257	ATCCTTGTATATTTA[C/T]TGAACTATGGAAGAT	9873
rs376681390	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72919953	AGAAAAAAATAGATA[C/T]AAAACAAAAGCCCTA	9873
rs376683085	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73072010	TATTTTTTGATCAGC[A/G]GTCAGGGCAGGGGAC	9873
rs376721409	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72850019	CATAGAAATGACTAT[C/T]TTTCGCACTTACATT	9873
rs376729911	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73114359	GGCCCAGGGCAGGTC[C/G]AGAAACGCTGTCCAA	9873
rs376735962	snp	C/T	0.0010855	0.0232716	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841587	GGAAGGAGAGATCTG[C/T]AGCAAAGGGAAGCGA	9873
rs376751741	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73085175	TAAAGACTCATGCTT[A/C]TTCAAGAGTGCTTCA	9873
rs376757976	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73116542	CTTCTTTCGTTTTTG[-/T]TTTTTTTTTCTTTGA	9873
rs376758400	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73124409	GAACTTAAAGTATAA[C/T]AATAATAATTTTAAA	9873
rs376772375	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72855234	GCTGAGATCGTGCCA[C/T]TGTACTCCAGCTTGC	9873
rs376782235	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126963	GAATTGCTGGAACAC[A/G]GGAGGCAGAGGTTGC	9873
rs376783595	in-del	-/AG			intron-variant	FCHSD2	GRCh38.p7	11:73057905	TTTTTTTTGAGACAG[-/AG]TCTCGCTCTGTCGCC	9873
rs376786680	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72988720	AATGTTCATTTACCT[C/T]CTTTTTCAAAATTCA	9873
rs376799687	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73127656	TAAACAGCTTCAGAC[C/T]TGATACTCTCAAGAG	9873
rs376799869	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73040955	TTTTTTAGCTCCCAC[A/G]TATCAGTGAGTGAGA	9873
rs376801969	in-del	-/CAA			intron-variant	FCHSD2	GRCh38.p7	11:72920598	TAACAACAACAACAA[-/CAA]AATTGTTCACTCAAA	9873
rs376804937	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72998858	AAATTGGAGCCCTTG[G/T]GCACTGTTGGTGGGA	9873
rs376826385	snp	C/T	2.25966e-05	0.00336122	intron-variant	FCHSD2	GRCh38.p7	11:72889779	AGTTCCTTAAACTGT[C/T]TGACATTTGGCTTAA	9873
rs376826474	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73067478	AACTTAAAGTATAAT[-/A]AAAAAAAAAAGAAAG	9873
rs376843544	snp	A/T	0.000390016	0.0139591	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141846	CCAAAGCCCCCCAGC[A/T]GCGCCCTTACCTTCC	9873
rs376844755	snp	C/T	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:73003529	TCTTGCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT	9873
rs376854635	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72992577	ATAGACCAATGGAAC[A/C]GAACAGAGCCCTCAG	9873
rs376873819	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72881037	CAGACAAATAGGACT[A/G]CATTAAATTAAAAAC	9873
rs376886418	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72958704	TCAGAGAAAGGTCTC[C/T]TATCTCCTTCCCAAG	9873
rs376887668	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73120114	CACCAAGAACAGCAC[A/G]GTGGAAACCACCCCC	9873
rs376893943	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73004019	GGAGACTGAGGCAGG[A/C]GACTCGCTTGAACTG	9873
rs376897053	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73048587	CTTTCATTCTGGGAC[A/C]CCATCTGAAGTAGTT	9873
rs376900869	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73080151	AAAATAAAAATACTA[C/G]ACGGGTATGGTGGCA	9873
rs376904269	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72893371	CCCAGGCTGGAGTGC[A/G]GTGGTGCAATCATGG	9873
rs376912275	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011048	CAGCTGTGATTGTAG[G/T]GGCAGGGGTGGGTAG	9873
rs376918746	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72851720	TGCACTCCGGCCTGG[C/T]GACAGAGCGAGACTC	9873
rs376924376	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72896014	ACTTTTATAGACAAG[G/T]GAAATTTTTGCCAAA	9873
rs376933062	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73080333	AAGAAAGAAAGAAAA[A/G]AAATTTTTCAAGGGT	9873
rs376961182	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72999641	AACATTCTTTGCCCA[A/G]GAATGTCAGTTAAAT	9873
rs376962688	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72904590	GTTTATAAATATTTC[A/C]GTATGACATCTAAAA	9873
rs376963310	in-del	-/CTCT	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72867380	TAAAACTCACCTACA[-/CTCT]CTCTATGTGAGGAGA	9873
rs376971494	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72889364	TCACAATTTTCTTTG[C/T]TAATTTTATGGTAAA	9873
rs376981337	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72963391	CAGCCTCATATTACA[C/G]ATGAGCTAAGTGAGG	9873
rs376985315	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73086116	ATACTTACATTATTT[A/T]ACAAGATGAGGCTGG	9873
rs376985892	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842303	TTAACCACAGAGCAA[C/T]GCCTTCCCTCTTCGG	9873
rs377006140	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931917	GCCATTGTTTCATTG[C/T]TGTTGTTTTAAATTT	9873
rs377012657	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73034528	CCAAGGAAATAGAGA[C/T]CAAAGTTTCCACTCT	9873
rs377015764	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72973232	ATTAGCTGGGTGTGG[A/T]GGCATGTGCCTGTAA	9873
rs377029329	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002987	TGGTTACAATAATAT[A/G]TGTTGAAGGAGTAAA	9873
rs377049362	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73097877	CAGAGTCTTGCTATG[C/T]TATCCCAGTTGGGCT	9873
rs377056635	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73038456	AAATGGGCAGTGACT[C/G]AAGATCACTCACCAC	9873
rs377062818	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73086740	ATAGAAGTAAAAAGA[C/T]TGTACAGAGTATTAT	9873
rs377080868	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894362	CCAGCCTGGGCAACA[C/T]AGCTAGACCCCAGCT	9873
rs377101234	in-del	-/GTTTT			intron-variant	FCHSD2	GRCh38.p7	11:72866271	TTTTTGTTTTGTTTT[-/GTTTT]TTTTGTTTTTTGAGA	9873
rs377109230	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72870857	GTGAGCCGAGATTGC[A/G]CCACTGCACTACAGC	9873
rs377115275	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72901249	AAAATACAAAGAAAA[C/T]AGCCAGGCACAGTGG	9873
rs377117989	snp	A/C/T	4.35713e-05	0.00466735	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841437	GCATTTAGACCCATG[A/C/T]CCAGGAGAACCCTTA	9873
rs377119952	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72966847	AGGAATATGATATAG[C/T]TTGAGGAAGGATTCC	9873
rs377120511	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965585	ATTTCTGAAACTTTT[A/T]GTTAAAGTATAACAT	9873
rs377121227	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72933676	CAAGTAATAATAATT[C/T]AATTGCTTTCCTTAC	9873
rs377136825	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73102840	TTATAAATTATCCAG[C/T]CTCAGGTATTCTGTT	9873
rs377145831	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72997745	TCCCTCTGTCATCCA[A/G]GCTGGAGTGCAGTGG	9873
rs377168813	in-del	-/TTAA			intron-variant	FCHSD2	GRCh38.p7	11:73130700	ACAAAAAAAGTTTAA[-/TTAA]ACAGACCCTCTCAAA	9873
rs377175988	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72976025	TATGAAAAAGGAACA[A/T]GTGAGGAACAAATTA	9873
rs377180154	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72958868	CATAAAAGGACATTC[C/T]AGTCTGCCAAAACAA	9873
rs377182532	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72998095	AAAAAAGGGTGGAAA[A/C]CAAAATGCTGAAAAA	9873
rs377184982	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72909262	GGCTGGTCTCCAGCT[C/T]TTGACCTCGAGTGAT	9873
rs377212987	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029321	GTCTCCCAACCTAGA[C/T]AACAATCACACTGCG	9873
rs377214009	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73107629	TCCAGTAAACTTCCT[C/T]CTACTCTCGAGTTCC	9873
rs377216154	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73077028	GGCAGGAGAATGGCA[A/T]GAACCCGGGAGGCGG	9873
rs377219319	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73041337	CTATACTAATTTACA[C/T]TCCTACCAACAATGT	9873
rs377234825	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848632	ATTGGGCACTCTATA[C/T]GTTTATTCAATGATT	9873
rs377235232	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72992794	ATGTTAGACCTAAAA[C/T]CATAAAAACCCTAGA	9873
rs377235812	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72905010	ACGTTTACTTCCATC[A/C]GGAAGCTTGCTTCTT	9873
rs377239317	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73035108	CTCAGGTTTAACTCC[C/T]GGACCTTGACAAGTT	9873
rs377243961	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73064001	CACTCTTCTTAGCAC[C/T]ACATCACACTTATTC	9873
rs377254910	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72922090	AGATACAGATTGTAA[C/G]TAAATATGAACAGTT	9873
rs377281883	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840105	CCTCCTAATCGCTCC[C/T]TATATCCTTTCTGCC	9873
rs377311663	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73101785	CAAAAATAAAAACAC[C/T]GATACCTATTCCAAC	9873
rs377320397	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73120713	CAGCCTGGGCAACAA[C/T]AGCAAAATTGTGTCT	9873
rs377330061	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124712	AGTGAGCTGAGATTA[C/T]GCCACTGCACTCCAG	9873
rs377335309	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73094317	GAACTCTAACATGCC[A/G]TTGGTGGGAATGTAA	9873
rs377337117	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73062242	AGGAAAACTAACAAA[C/T]AGAAAGGAATAGCAT	9873
rs377341114	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73029640	AGGAAGTCATTGCAG[C/T]ACCCTTTCCCTATTG	9873
rs377374757	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72942521	TGTATATGTAATACA[C/T]GCCTAGGAAAGATTA	9873
rs377434750	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088625	TTTAAAAAAAATGCA[C/T]ATTCATAAACATGTA	9873
rs377439592	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72993883	TGCACGTTGTGCACA[C/T]GTACCCTAAAACTTA	9873
rs377444126	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73075553	AACAGTTTGATCATT[C/T]GTTAAAAAGTTAAAC	9873
rs377446138	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72977809	CGAGCAATCCCATTA[C/T]TGGGTATATACCCAA	9873
rs377461624	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73044783	ATCATCTAACACTAA[A/G]GATGGGGCTGGGCAC	9873
rs377472581	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72992753	ACCTTATACAAAAAT[C/T]AATTCAAGATGGATT	9873
rs377475495	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72909825	GAGAAGTGAGGAGCA[A/C]CTCTGCCCGGCAGCC	9873
rs377484374	snp	C/T	0.0036988	0.0428453	intron-variant	FCHSD2	GRCh38.p7	11:72984252	ATAATCAGTGCAAAC[C/T]GATATTGTACTGCAA	9873
rs377502346	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73043061	TCTTTCTCTTGACTG[A/T]TGCTCTGGCTAGAAC	9873
rs377504447	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72965235	GTACATTATACTGTA[A/G]AAATATTGAACTACT	9873
rs377509184	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987297	AACATCACTTCTTCT[A/G]TAAAGCTTTCATTTA	9873
rs377510266	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005375	ATGGCTAGTCCAAAT[A/C]GTTCAAGTCTTGATT	9873
rs377519029	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73021803	CGGATATATACAAAA[A/G]ACTGGCTGGGCGTGG	9873
rs377532751	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72902166	AAGCGTGAGCCACAG[C/T]GCACGGCCTACTCTG	9873
rs377534328	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72915691	GGCGCGGTGGTGGGC[A/G]CCTATAATCCCAGCT	9873
rs377537934	snp	A/C/G	0.000149055	0.00863188	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72984146	TGTGCATTTGCTGCC[A/C/G]CTAGGGTAAGAAGAT	9873
rs377558770	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72897316	AATATTTTTTAAAAA[-/G]AGTAAAAAAAAAAAA	9873
rs377561905	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73118084	CACTTTGGGAGGCCA[A/G]GGTGGGCAGATCACT	9873
rs377583611	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837465	ATTTCTTAACCAAGG[-/A]AAAAAAAAAAAAAAC	9873
rs377728144	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986309	CTGCCTCCTGGGTTC[A/G]TGCCATTCTCCTGCC	9873
rs377728258	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72948879	ACCACGTTAGCTAGG[A/G]TGGTCTGGATCTCCT	9873
rs377732924	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023634	TTTTGAAATTTCTTA[C/T]GAACAGAGACTTCCA	9873
rs377733683	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73068245	AAAAATATGCCATTA[A/T]GTGCATGTTCTCGCT	9873
rs377737266	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72988209	ATCAGTCAGCACACT[A/G]ACCCTGAGTCTCAGC	9873
rs377759935	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72859988	GGACTGGACCCTTGG[C/G]GTACCATGAGGGAAG	9873
rs377764706	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73021138	CACCTCTGCCTCCCA[A/G]AGGGCTGGGATTAAA	9873
rs386374144	in-del	-/AA			intron-variant	FCHSD2	GRCh38.p7	11:72900676	AAGCTGATTTGATTA[-/AA]AAAAAAAAAAGCACT	9873
rs386374145	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72907600	GATAATCACGTGGGT[-/TT]TTTTTTTTTTTTTTT	9873
rs386374146	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72907618	TTTTTTTTTTTTTTT[-/TT]TCTTGAGACGGAGTC	9873
rs386374148	in-del	-/AGGA			intron-variant	FCHSD2	GRCh38.p7	11:72966207	TCTGTCGCCCAGGAA[-/AGGA]GGAGTGCAGTGGTGC	9873
rs386374149	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73039250	CTGCAGGGTGCAGTG[-/G]CTCACACCTGTAAGC	9873
rs386754897	multinucleotide-polymorphism	GTT/TTC			intron-variant	FCHSD2	GRCh38.p7	11:72851217	TTGAAAAAACAACCT[GTT/TTC]CACTGAAATTAAAAA	9873
rs386754898	in-del	G/TT			intron-variant	FCHSD2	GRCh38.p7	11:72885242	GGAAACCAAGTGAGA[G/TT]ATTTTATGCTAACAG	9873
rs386754899	in-del	CTC/GAGA			intron-variant	FCHSD2	GRCh38.p7	11:72889462	ACACTGCTGAGTGTT[CTC/GAGA]AAGTACAGAAAAAAC	9873
rs386754900	in-del	AT/TTA			intron-variant	FCHSD2	GRCh38.p7	11:72928510	CTTCCACTTAAATAC[AT/TTA]AATGATAATGATGGT	9873
rs386754901	multinucleotide-polymorphism	CTG/GTA			intron-variant	FCHSD2	GRCh38.p7	11:72928677	TTGAATCTTATTTAA[CTG/GTA]GGTGAGAGGAGGCCC	9873
rs386754902	multinucleotide-polymorphism	CT/TC			intron-variant	FCHSD2	GRCh38.p7	11:72988385	TCTTTTCCTACTTAT[CT/TC]TTAAAAAAAGGTCTT	9873
rs386754903	multinucleotide-polymorphism	AA/GC			intron-variant	FCHSD2	GRCh38.p7	11:73023467	TGTCATTACGGAAAT[AA/GC]AAACTAAAATAATGT	9873
rs386754904	in-del	AAAC/GTT			intron-variant	FCHSD2	GRCh38.p7	11:73042237	GCTGAGATTATTTTT[AAAC/GTT]TCTGGTGAAAGACAG	9873
rs386754905	multinucleotide-polymorphism	CTG/TGT			intron-variant	FCHSD2	GRCh38.p7	11:73062204	CAAACTTCAGCAGAC[CTG/TGT]CAGCAGAGGGGCCTG	9873
rs386754906	multinucleotide-polymorphism	CGT/TGG			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140418	CACAAGCTCAATCCA[CGT/TGG]CTAGGTCTTCCTACA	9873
rs397727172	in-del	-/GA	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72885241	GGAAACCAAGTGAGA[-/GA]TTATTTTATGCTAAC	9873
rs397743939	in-del	-/TCCT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72966210	ATCGCACCACTGCAC[-/TCCT]TCCTTCCTGGGCGAC	9873
rs397743943	in-del	-/A	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72861949	AAAAAAAAAAAAAAA[-/A]GATAATATATCATTA	9873
rs397747922	in-del	-/CT			intron-variant	FCHSD2	GRCh38.p7	11:72985695	AAAGTCCTGGGACTC[-/CT]TGCCCTGTATGATGT	9873
rs397748520	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73132842	AAAAAAAAAAAAAAA[-/A]CCTCAGGTGATTCTT	9873
rs397748721	in-del	-/CT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72985696	AAGTCCTGGGACTCT[-/CT]GCCCTGTATGATGTA	9873
rs397752452	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72953638	GGGGGAAAAAAAAAA[-/A]CACAAAAACTCTTGC	9873
rs397757720	in-del	-/AA	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72900686	GATTAAAAAAAAAAA[-/AA]GCACTACTATAAAGG	9873
rs397766521	in-del	-/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72898746	TTTTTTTTTTTTTTT[-/T]AAAGACAGGGTCTTG	9873
rs397793205	in-del	-/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72962611	CCCCCTTTTTTTTTT[-/T]AAACTAAGAATGTTC	9873
rs397820243	in-del	-/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72892918	GGTAATTTTTTTTTT[-/T]AAGACAGTGATATTA	9873
rs397848524	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73111476	TCCTTTTTTTTTTTT[-/T]CAGTCTATGTGTGTC	9873
rs397848553	in-del	-/AC			intron-variant	FCHSD2	GRCh38.p7	11:73121191	CACACACACACACAC[-/AC]GCATGCACGCACACA	9873
rs397849002	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73108562	TTAAGTTTTTTTTTT[-/T]GTTTGTTTTTTGTTT	9873
rs397849055	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72861410	CAAAAAAAAAAAAAA[-/A]CTCCAGGACCAGATA	9873
rs397849152	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73046007	TTTTTTTTTTTTTTT[-/T]AGAGACAGGGTCTCA	9873
rs398016628	in-del	-/AAA	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72938198	GCAAAACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA	9873
rs398016629	in-del	-/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72956838	GTCTTCTAGGGTTGG[-/T]TTTTTTTTTTTTTCC	9873
rs398016630	in-del	-/A	0	0	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143611	ACAGCCCCGTGACTC[-/A]AAAAAAAAAAAAAAA	9873
rs398055242	in-del	-/TTTTTTTTTTTTTTTTTT			intron-variant	FCHSD2	GRCh38.p7	11:72916985	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTT]GAAGCAGAGTGTTGC	9873
rs398076031	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72898745	TTTTTTTTTTTTTTT[-/T]TAAAGACAGGGTCTT	9873
rs398076032	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72956837	TGGAAAAAAAAAAAA[-/A]ACCAACCCTAGAAGA	9873
rs398076033	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72957031	AGTCTTTTTTTTTTT[-/T]TCTTCTTTTTTTTTA	9873
rs398076034	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73116958	TTTTTCCCCAAAAAA[-/A]ATCACTATTGTTATA	9873
rs398115498	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73039528	CTCCAAAAAAAAAAA[-/A]GAAAGAAAGAAAAGA	9873
rs527254458	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73044823	CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA	9873
rs527281722	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944661	AAACCCCATTGTCTC[A/G]GCTCAAAATCTCCTT	9873
rs527286541	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72845797	CTTAGATTACTGTGG[A/G]TTTAAGTCCAGCTTC	9873
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	9873
rs527300183	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093307	AATCATAACCTTACT[C/G]AGTAAACTTTCAGTG	9873
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	9873
rs527306373	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101251	GTTGCACAGAAAATA[C/G]ATTGCATAAGAGCAA	9873
rs527309727	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945415	AAGATGGGTTAAAGA[C/T]TTAAATGTTAGATCT	9873
rs527319341	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937538	GGACCATTAATGGAA[A/C]GGCAAGGTCTGATCT	9873
rs527322784	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038089	AAACAAAACCATCTA[C/T]CACTAAAAAATTCTT	9873
rs527327047	in-del	-/TAAA	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72985179	TCACAATAAAATTAC[-/TAAA]TATATTATTAAAATT	9873
rs527337922	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72893316	CCTAGATCATTCTTT[C/T]AACATTTTTCTTTTT	9873
rs527349596	snp	A/C	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72992673	AACGATTCCCTATTT[A/C]ATAAATGGTGCTGGG	9873
rs527355810	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72884713	AGGATCAAGCCTCTG[C/T]CTCCCAAGTAGCTGA	9873
rs527386964	in-del	-/TC	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72968334	ACTATAATTTATCAT[-/TC]TGTTTCCTAGAAAAT	9873
rs527400247	snp	G/T	0.029116	0.117091	intron-variant	FCHSD2	GRCh38.p7	11:72938186	AAGGAGTTTTTTTTT[G/T]TTTTTTTTTTTTTTG	9873
rs527402881	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930161	AAAGCACTTAGGGCA[C/T]ATAATGTTGCTCCAT	9873
rs527405468	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73070423	AATGTCAGGGTTTTT[C/T]ATTTTTATTTTTATT	9873
rs527405487	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73129465	CAGCATTAGATTCTC[A/G]TGGCACGAACCCTAT	9873
rs527415730	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73074089	CAGTGTGATATCGGG[-/A]AAAAAAATATTTCAA	9873
rs527427328	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72885511	CTAAATGAAGACTCT[A/G]TGTGCCTGATACCTA	9873
rs527428549	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122517	ACAGGAATGGCTACT[A/T]GTAAGAAATGGCCTG	9873
rs527429814	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72877509	TTTTAATATTTTTAC[A/C]CCAGATTAATATTGT	9873
rs527436715	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73086080	AGAAAGCAGTGCTAC[A/G]GGGGAAATTTATAGC	9873
rs527438146	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930850	CTAATGGGTACAAAA[A/C]AATAGAATAAGACCT	9873
rs527441740	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73123636	GTCATCACACTATAA[A/T]GGCAATATTCAGGAA	9873
rs527442516	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72941155	CTCATAATTTAGGAC[A/G]GTCAAAAAAATAAAT	9873
rs527459024	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031549	GTAATGCCAACATTT[G/T]TACTGGGTGTTACAC	9873
rs527465850	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878222	AGTTCAAGGCTATAG[C/T]ACACTATGATTGTGC	9873
rs527485065	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73086524	GCAGAAAGAAGGAAA[C/T]ATTAATAATAAAGAT	9873
rs527485142	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73077409	TAAGAAGACTATATC[C/T]AGTGTTGAGGAAGAC	9873
rs527557482	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72871306	TTGAAAATCTGCCAA[A/T]CCCTGACATTCAAGC	9873
rs527563693	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72968139	AGCATATAAGGCCTT[C/T]GGAATTATCTTGAGG	9873
rs527569749	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72974458	TTAGGTTTCCAACAC[A/C]TGAACTTTAGAGGAC	9873
rs527575711	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914839	GCAAAGATTTCATGA[C/T]GAAGATGCCAAAAGC	9873
rs527583999	in-del	-/ATG	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73028659	TGGGCCAGGGGTGGA[-/ATG]ATATGGTTTGGCTCT	9873
rs527588334	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870682	GAGGGGGGCAGATCA[C/T]GAGGTCAGGAGATCG	9873
rs527591234	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72897214	TAAATGCTTAGTATC[C/T]TATTTAATTTTCAAA	9873
rs527595471	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72960413	ATGCTCTAGTCTGCT[A/G]CTCCTTTGGATTTAA	9873
rs527610222	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73070170	GCCTTCATATAATGG[C/T]CTATTAATGACATGG	9873
rs527622272	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047627	AAAACTGTTCCATGA[C/T]TTCTAACGGCAAATA	9873
rs527631637	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862171	AACTTCATACTTAAT[A/G]GTGAAAGACTGAATG	9873
rs527636874	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017096	CAAACAATCCTCCCA[A/G]CTCAGCCTCCCAAGT	9873
rs527638917	snp	C/G/T			intron-variant	FCHSD2	GRCh38.p7	11:72969855	ACACATTGGTTATGC[C/G/T]AGGTACAACACGACC	9873
rs527639303	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72929362	CCCAGAATTCCCTGA[A/G]TTTTAATTACCACCT	9873
rs527639565	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72862886	GGACAAACAGATCAA[C/T]AGAACAGAACAAAAT	9873
rs527645855	snp	A/G	0.00835141	0.0640778	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144009	GGCCCTGACAGCTGC[A/G]GGGTGGCAGCTAGAG	9873
rs527655535	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908954	CCATTGCATGTTGCC[C/T]TGTCTGCTATTTATA	9873
rs527673570	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73062216	GACCTGCAGCAGAGG[A/G]GCCTGTCAGAAGGAA	9873
rs527674163	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73136747	TAAAAACCCAAGTTC[A/G]GGCCAGGCGCAGTGG	9873
rs527684488	snp	A/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:72961244	AGTACTTTTTGTTTG[A/T]TTTTTGAGACAGAGT	9873
rs527692452	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909245	TTTCGCCCTGTTGAC[C/T]GGGCTGGTCTCCAGC	9873
rs527700181	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72967181	CTCCAGCCTGGGCGA[C/T]AGAGCAAGACTCTGT	9873
rs527702324	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854945	GAGTTCGAGACCAGC[C/T]TGGCCAACATGGTGA	9873
rs527702414	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73135886	TAAGGGGTGCGTTGC[-/A]GCAGTAGTGGCTCAT	9873
rs527706491	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008139	AGGCCAGGAGTTTGC[A/G]ACCAGCCTGGCCAAC	9873
rs527721273	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953519	TAAATCAATTTCAAC[C/G]ACATGAATTTATTGA	9873
rs527729071	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144033	GCTAGAGCCCAGGCC[A/G]TAGGTAGCGTAGGCT	9873
rs527734343	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054839	GTGGGCCTGGTGGCA[C/T]GTGCCTGTAATCTCA	9873
rs527735907	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062701	CCAGTGATTGAAGAT[A/C]AACTTAATGAAATAA	9873
rs527746800	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72965358	TGAATTTTTACTGAG[C/T]GCTCTTCTATGCACT	9873
rs527760608	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010281	CTCTTTGGTAAATTT[C/T]TCATTCATATCCTGA	9873
rs527764167	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73001296	ACATAACAAGCAACA[C/T]GGCATATACTCTATT	9873
rs527768471	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73003233	TAGCACACTTCACTA[C/T]ACTTTCATTTCCTCA	9873
rs527775949	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102485	AAACTGAAAGCAATG[A/T]AACGAAACATCCATC	9873
rs527804106	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72946054	TTACCGAGTATATAC[C/T]CAAAGGATTATAAAT	9873
rs527810701	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055336	CAACAGAGTGAGACC[C/T]TGTCTCGAAAAAAAA	9873
rs527817955	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72894655	AAGCATCTGGATCTC[C/T]GTATTCCAACTACAC	9873
rs527822837	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994091	TCTCACTCCCTTGTC[C/T]TAGACCTGTCACTTG	9873
rs527826739	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73038103	ATCACTAAAAAATTC[G/T]TATGACGAGGTGGGA	9873
rs527839040	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939375	TCAAAAACCTTTCTA[A/G]GGAATGGTTTTTAAA	9873
rs527842311	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73103279	AGAAAAAATAAAACA[A/T]AATAAAAGTTGTAAA	9873
rs527860429	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72903646	GGCATCTGATGGGGC[-/A]AAAAAACCCCACTTT	9873
rs527863709	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73107101	CAGTGCAGTGGCGCA[A/G]TATCGGCTCACTGCA	9873
rs527877908	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839869	CATTCGGCAAGAGTG[C/T]GTTCAACAACTTCAA	9873
rs527879790	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848313	AATTTAACATTTCCT[A/G]AACACCCCACACTCT	9873
rs527887207	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113712	AGGCATTTGAAGAAA[C/T]ACCCATTTGTACCCA	9873
rs527889471	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994568	CCATGTTTTAAGATA[C/T]AGTGTAAACTCACGG	9873
rs527897973	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840550	CAAATAGAGGCCTGG[A/G]AAATTAAATGCTTAC	9873
rs527903420	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886428	CTTCTGTGTTACACC[C/T]GCAACAATCCCTCCC	9873
rs527908992	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72932756	TTTTTGTTTAAGTTC[C/T]ATAAAGGGAGGCATC	9873
rs527919105	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73040371	AGTGTTTTCATTAAG[A/G]GCACTATTACAATAC	9873
rs527937884	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72962855	CTGCCACAAAAGTTA[A/G]ATATCTTGATTTCAG	9873
rs527947916	snp	A/G			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144352	AACCCCGTCTCTACT[A/G]AAAATACAAAAAATT	9873
rs527948536	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72986917	TAATGTTCCTTGGGG[C/T]TCCAAACTCAACTTC	9873
rs527959956	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087757	AGCCTAAGTGTATAG[C/T]GTAATAAATAAACAG	9873
rs527976883	in-del	-/TGTT			intron-variant	FCHSD2	GRCh38.p7	11:72932781	GGCATCAGGTCTGTC[-/TGTT]TACCATTCCATCTTC	9873
rs527996022	snp	A/C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932704	CCTGATCATAGCATA[A/C/G]AACCTCATACTGGTG	9873
rs528006420	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72958384	TTAGCTGGGCATGGT[A/G]GTGCTGACCTGTAGT	9873
rs528013212	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73079755	GGAGAACATTAAAGA[A/G]TAAGAAGAACTCAGA	9873
rs528022687	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73119906	TAAAGACATACCTAA[C/G]ACTGGGCAATTTACA	9873
rs528032944	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72866381	TTCAAGCGATTCTTC[C/T]GTCTCAGTCTCCTGA	9873
rs528033852	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72879761	TGTGGAATGAGCTTT[A/G]CATATGACATGTAGG	9873
rs528038861	snp	A/C	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72987693	CTTCTCAGAAACGCC[A/C]CTCCACTGTGCTCAT	9873
rs528044878	in-del	-/C	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73101522	ATGGCTCACTGCAGT[-/C]TCCATCTCCTGGGCT	9873
rs528049254	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72890111	AGAAAGTTACCAGAA[A/G]AGTAAGATCAGCATA	9873
rs528052095	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911258	TTGTCCTTTCTCCAA[G/T]GTATGTTCTTGACAA	9873
rs528056235	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72861109	AAAATCAATAAAATC[A/G]AAAGCTGATTCTTCA	9873
rs528057618	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134938	CAACCTCCACCTCCC[A/G]GGTTCAAGTGATTCT	9873
rs528078531	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73133346	CATTATTAATAATAG[C/T]AAAAAGTAGAAACAA	9873
rs528089606	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73013097	CAACACCTCCATTAC[A/G]TTCTGAATAAAAAAG	9873
rs528118235	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72856894	CTTAGAAGACATTGC[C/T]TTCATATTCTAGGAA	9873
rs528121165	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73141011	TTAGGCAAATGTTTG[C/T]CCACGAGGGGAGGAC	9873
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	9873
rs528146605	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096601	TATACCACTTCCAGA[C/T]AGAATTATAGAATGT	9873
rs528149022	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058207	TTAAAGGTATTGGAC[C/G]ATTATTGTTTTATGT	9873
rs528152151	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73013870	CTCCCATCTTAGCCT[C/T]CTAAAGCACTGGGAT	9873
rs528161283	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956656	GAAAGGGCAAGAGGT[C/T]TCTCTGGGACTTCTT	9873
rs528164962	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004681	GGTTAAATCTAAAAC[G/T]GTTTACATCACATCA	9873
rs528171013	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905791	TTTTATGGCTGCATA[C/G]TATTCCATGGTGTAT	9873
rs528194906	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72963965	CTAATTAATAGATGG[C/G]TAAACTTGGAAGTAG	9873
rs528196435	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949431	CTCTAGCCTGGGCAC[C/G]AAAGAGCAAAACTCC	9873
rs528199377	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72957511	AAAAAAACTGAGGAA[C/T]TCTTCTAGATTGAAG	9873
rs528207473	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72906439	GTTTAATTAGATACT[A/G]TTTGTCTATTTTGGT	9873
rs528223492	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72897987	TTTAGAAATCAGTAA[C/T]TCTCTTATGGAAATA	9873
rs528226975	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850827	GTGTGTGGTGGCTCA[C/T]GCCTGTAATCCAAGC	9873
rs528268435	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950438	CTTGCATTTTTTTTT[C/T]CCCTCAAAGAGTTTT	9873
rs528280028	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942549	TTAGAAGGATATGCC[A/C]AGATGACAGTAAGAG	9873
rs528290418	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851501	ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGCG	9873
rs528290577	snp	A/G	4.94393e-05	0.00497164	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843210	GTGGAATTGCTGGAC[A/G]TGTGTGACCGACTGT	9873
rs528302859	snp	A/G	0.00318978	0.0398085	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72844137	TCCTGCCATTTTCTG[A/G]AGGATGTGAGTCAAT	9873
rs528303581	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72943241	CATGTGATCTGCCCA[C/T]CTCTACCTCCCAAAG	9873
rs528310257	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73043221	TATTTTGCTGAGGTA[G/T]GTTCTTTCTATGCCC	9873
rs528313197	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098856	CCTTGGATTTTGCAA[C/T]GCATTCCTAGATGGG	9873
rs528322645	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071446	CCTGTAATCCCAGCA[C/T]CTTGAGAGGTCGAGG	9873
rs528335100	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72859925	AGAACAGCTGTCCCC[A/T]ATCTTTTAGGCACCA	9873
rs528356293	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990323	ACCCTGGTAGGCAAA[C/T]TGCATCAATTTGGGA	9873
rs528373245	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73043986	CAAACTATTAGGTGA[C/G]TGAGAAATAAATTTC	9873
rs528385735	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936030	AAAACATCATGGGCA[A/G]CAGAAAACCTTGAAC	9873
rs528410608	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117135	AGAAGCTGGTATTTA[C/T]AAGCTGGTACTTATA	9873
rs528414941	in-del	-/TTTC	0.00244848	0.0349033	intron-variant	FCHSD2	GRCh38.p7	11:72897375	CATGTACAGACTTTT[-/TTTC]TTTGTCTTATTTCCT	9873
rs528417004	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73092261	GCCTCCCAAGTAGCT[G/T]GGACTATAGGTGTAC	9873
rs528428539	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928268	ACAAAATTTTTTTCA[A/G]TGGCTCCCACTGTAT	9873
rs528440829	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882964	ACTGGCATAAGTACA[G/T]ACATATAGACCAATG	9873
rs528451507	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029101	GCACCATAAATATAA[C/T]GGTGTAGTACACTAA	9873
rs528465730	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124340	GGTGCAGCACACTAA[C/T]ATGGCACATGTATAC	9873
rs528468743	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883471	AAGACCAATCTAAAT[C/T]TGGGCAAAAGATATT	9873
rs528532744	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72919590	TCATGGGATTCAAGA[C/T]ATATCCCATGCTAAA	9873
rs528538343	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73075303	AATTCCATTCCTTAG[A/G]TAAATACCCAATAGA	9873
rs528541458	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72849093	TGGCGGAGGAGTGAA[C/T]CTGGTGCATGACAGG	9873
rs528561336	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72920718	TACATTAAAATCAAA[A/C]AAATTATACAGTAAA	9873
rs528576961	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72981641	TGTTCTTTGAAACTG[C/T]TGGTCCTTGTAAGTC	9873
rs528586277	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73043366	GTATTTATCATCCTA[A/T]CCACTTTTCTGGGCA	9873
rs528588470	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131445	GAGGCAGGAGAATGG[C/T]GTGAAACCAGAAGGC	9873
rs528590123	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022884	GATCCCAGAAATAGA[A/C]CCATACAAATATAGT	9873
rs528598150	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076046	ATCACCTGAGCCCCC[A/G]GGAGGTCGAGGCTGC	9873
rs528604944	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72846418	AACTCCTGACCTCGC[A/G]ATTCGCCCGCCTTGG	9873
rs528610576	snp	A/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73139539	TAACCTCAATAATAA[A/T]ATAAAATATGATAAA	9873
rs528622406	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73102440	AAATGTGTACAAAAT[A/G]TGTACAGCAGCATTA	9873
rs528629275	in-del	-/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73047238	TTGTTAAAACTACCA[-/T]TTTTTTTTTAATTAA	9873
rs528646565	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014953	GGTTCAAGCAATCCT[C/T]CTGCCTCAGCCTCCT	9873
rs528651503	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913626	TATTGTTCACAGTAG[C/G]CTCTAATGGTCCTTT	9873
rs528663898	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138757	GGACTACAGGCGCAC[A/G]CCACCATGCCTGGTT	9873
rs528680792	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72852279	CTGCTGGTGGGAGTA[C/T]AAATTAGTTCAGCCA	9873
rs528683330	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73060125	ACCTCTGTGACTCTG[C/T]TACTGTATAAGGAGT	9873
rs528705342	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860943	AGCACTTAATGCCAA[C/T]ATTCAAAAAGAAGAA	9873
rs528708131	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907432	TCAAAGGGAATGCTT[C/G]CAGTTTTTGCCCATT	9873
rs528725437	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72959391	CCCGCCACCATGCCC[A/G]GCTATTTTTTTTTTT	9873
rs528741358	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061033	GGCAAGATGGCCAAA[C/T]AGGAACAGCTCTGGT	9873
rs528764503	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951870	TAGCGTTCAGTATAG[A/C]AGAGAAAGTCCTTAC	9873
rs528777655	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72990870	GACCAGAACAGAACT[A/G]AACGAAATAGAGACA	9873
rs528789724	snp	C/T	0.000128016	0.00799949	intron-variant	FCHSD2	GRCh38.p7	11:72900225	AACCCACACTTCCCA[C/T]CCCTCCCGCCCTTGA	9873
rs528793043	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72845071	CCAGACGTTAATGTA[C/T]GTGACAGCAAACCAG	9873
rs528805420	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73061290	GATACTGTGCTTGTC[A/G]CATGGTTTTCGCAAA	9873
rs528809365	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939956	GTAGTAAAGTTCCAG[A/G]GAGTTTCTTCGAGAA	9873
rs528814150	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853143	TCTTGCACTTAAAAG[C/T]TTTTTTAAAAATTGA	9873
rs528826706	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72900696	AAAAAAGCACTACTA[C/T]AAAGGGCAAAGGTTG	9873
rs528828070	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028599	GGTGGACTGTTGAGA[C/T]GGCATGATTGTGTTT	9873
rs528847471	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72860143	GCCTGCTGGTCTGAC[-/A]AGGACGCAGAGCTCA	9873
rs528850475	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040293	AGAAGCTGTAATTGT[C/T]TCGCAGTCATGTGGA	9873
rs528866332	snp	A/T	0.0298908	0.118541	intron-variant	FCHSD2	GRCh38.p7	11:73087721	AAAAAAAAAAAAAAA[A/T]TTTTAAAATAAATTT	9873
rs528868877	in-del	-/TTG			intron-variant	FCHSD2	GRCh38.p7	11:73101431	GTACTCTTGTTGTTA[-/TTG]TTGTTGTTGTTGTTG	9873
rs528876081	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878936	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	9873
rs528878659	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139858	CCCCCACTGAAGGAA[A/G]AAGTTTGTATTGTGT	9873
rs528905318	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72908192	CCAGTTTTATCTATG[C/T]TGTTGTAAATGACAG	9873
rs528910007	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856661	CAGCTGAGTGAGGAA[A/G]TCCTGTGCTATCTCT	9873
rs528911937	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033171	CGGGCACCTGTAGTT[C/G]CAGCTACTCGGGAGG	9873
rs528922558	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72894571	TCTTTATGAAGTATA[A/T]TAATATATGGTTAAT	9873
rs528927999	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73138541	ATTTCTTAGTTTGCT[C/T]AATAAGTTAAAAAAA	9873
rs528963940	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879635	AAAATTCACAAGATG[A/G]CCTTAACAGTAGTTT	9873
rs528968552	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73136019	TTTAAAATAAGCCAG[C/G]CATGGTGGCACGTGC	9873
rs528969720	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72924484	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	9873
rs528987693	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72928750	ATTATACTTTAAGTT[G/T]TAGGGTACATGTGCA	9873
rs528988481	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72871925	CCCTCCGAATTCTCT[G/T]CTTGGGGAGTTGATA	9873
rs528989747	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025999	GATTCATTTTATGTA[C/T]GTATGTATGTATGTA	9873
rs528992350	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72969799	TGATAAAGAAGCAAA[A/T]TTCTTAGGCTTAAGT	9873
rs529030676	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970611	AGCCACTGGTTTCTT[C/T]TGTGCATTACTTTCA	9873
rs529042770	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863679	TAAAAATTAAACAAA[C/G]ATTTGAACAGACACT	9873
rs529074152	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855886	TGCTTTTTATATACA[A/G/T]CTATACTCTTTGAAC	9873
rs529098976	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72864238	AGAACAGGGTGGGCA[C/T]AGTGGCTCATAAATA	9873
rs529107078	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73116990	CTCTGTTTCATTTTT[A/G]GCATATTGATTTTTA	9873
rs529116316	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72963151	TGTTTTTAAAAAAAT[A/G]TTGTCTTTGTTTCAC	9873
rs529117284	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018944	GGTTCAATTAAGTCA[A/G]GATCTCAGAATTCAA	9873
rs529120593	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73023785	GTGAATGGATAAACA[A/C]ACTGTGGTACATAAT	9873
rs529144875	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954311	ACACCTGGGCTCATG[A/C]AATTCTCTCAACTCA	9873
rs529145343	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111188	ACTACCAGGTCCATT[C/T]GGTCTATAGTACAGA	9873
rs529148049	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73063721	TTGGTAAAGTGATCA[A/G]TGCAGCAAGAAGAGC	9873
rs529152265	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73072999	CAAGGAGCCGCCCTT[A/G]AAGTCCACAATGTTT	9873
rs529164342	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73010951	TCTGGGTCTTGAGCA[C/G]TGTATGCTGGTGTTG	9873
rs529164686	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084725	GTATTAACATTTATG[A/T]TACTGGAATGCATCT	9873
rs529168014	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73038624	TACCACATGTTCTCA[C/T]ATCTAAGTGGGAGCT	9873
rs529171919	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116521	GCATTATCAAAAGTC[A/G]TAATTCCTTCTTTCG	9873
rs529200649	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72910103	GGAGCCCCTCTGCCC[A/G]GCCACCCATCGTCTG	9873
rs529201226	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73070325	CTGATAACATTCCAG[A/C]ACTAAACAGCCTATA	9873
rs529203529	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73123667	TTTGAATAAACTATA[C/T]GATCTTCTTAATTGC	9873
rs529205894	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104370	CTCCCAGGTTCAAGC[A/G]CTTCTCTTGCCTCAG	9873
rs529214660	in-del	-/A	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72989417	ACTGTTGGAGATATC[-/A]ATGATAATAAAATCA	9873
rs529226200	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002752	CAGTCTCAGTTTAAA[C/T]GTAACTTCCTTTGGG	9873
rs529244356	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72849203	GCAAGAGAAGATTCA[C/T]GTATTCACGCCTCCC	9873
rs529250453	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995176	ATTCCTTTTTATCGC[C/G]GAATAGTATTTTGTT	9873
rs529255697	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73032551	ACTTAATTGCTCAGT[A/G]TTTTTAAAGCAAATG	9873
rs529267866	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73104853	CTGAGTCACCGTGCC[G/T]GGCCAACTTTACTAA	9873
rs529295576	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841287	TATGAGCCGTGATCA[C/T]GCCACTGAACTCCAG	9873
rs529296970	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72948377	AATTACTGAATGTTT[A/C]ATTTTTCAACATTTT	9873
rs529312933	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041169	ATAACTTGGCTACTA[G/T]GAATAGTGCTGCAAC	9873
rs529313012	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73042921	ATCCTGCAATTCTAC[A/T]GAATTCATTTTTCAG	9873
rs529322293	in-del	-/TTC	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73044747	TGCAATAATTTAACA[-/TTC]TTCTAGCATGTTATA	9873
rs529322977	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72896983	AGGTGCCCGCCACCA[C/T]GCCCGGCTAATTTTT	9873
rs529331809	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940891	TACAAATTTTTTGAG[G/T]TTATCCTCATTGATC	9873
rs529335034	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987898	GTTCACTGACTCTAT[A/G]AAAGTACAGGAAATA	9873
rs529343015	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842014	GGGTCACAATCACCA[A/C]GCAAACAAGATCGGC	9873
rs529372004	snp	C/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:72988386	CTTTTCCTACTTATT[C/T]TTAAAAAAAGGTCTT	9873
rs529381459	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72852163	CAAATTGCTAAGATT[A/G]TAGGAGTGAGCCATC	9873
rs529390176	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880549	ATATCCACCTGCCAA[A/G]GAATGAAACTAGATC	9873
rs529412122	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041922	TAATCCACTTTGAGA[C/T]TATTATTATTTATTT	9873
rs529420680	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941466	GCTTAGTATAAAATA[C/T]AGACTCCCAACTCTA	9873
rs529422389	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72933494	CTTAGCCAACAAATT[C/T]CTCTGTTTTGCCTAA	9873
rs529427160	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881417	GATGCAGAAAAAAGG[C/G]AACTGTTATACACTG	9873
rs529459283	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72924779	TAGATGACACCATTG[A/C]GCACTTCAAATTTAG	9873
rs529475500	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027746	TAGGAAGGAAAAATG[A/G]TTTTGTAGCCCAGGA	9873
rs529494488	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73035223	ACTAAGACAAGGTCT[C/T]GCTCTGTCACCCAGG	9873
rs529504221	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980436	ATTTCATTTGAAGAA[A/G]GGCAAAGATAAGAAT	9873
rs529520714	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081826	AAACCAGATAACATA[C/T]ATAAAATACTCAGAG	9873
rs529546956	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72874719	ACATGGTATTTGCCA[A/G]CTCAGATTTAGACTG	9873
rs529554223	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73028245	GTACCCTGCAGAGCC[A/T]CAAGGACAGAGATGC	9873
rs529559659	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73007519	GCAGGAGGTGATGTG[A/G]AAGGATCACTTGGAT	9873
rs529565771	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72961560	CATACCTGGCCTACT[A/G]TTGTTTTAAATGCGG	9873
rs529568216	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73032717	CCCAAAGGAAATGAA[A/C]ATTGACATCTAAAAA	9873
rs529597447	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927353	ACTGAGAATGTACAA[C/T]ACAAAGAATGAGCCC	9873
rs529600275	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72972054	TTGTACCTCAATAAA[A/G]TTGATTTAAAAAGAG	9873
rs529601805	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73107296	CTTGTGATCTGCCCA[A/G]CTCGGCCTCCCAAAG	9873
rs529620398	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006452	TCCTCATTTGTCTAT[A/C]ATATCTGCTCCATCA	9873
rs529648284	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951311	AGTGGCAGAGTTGTA[A/C]GCAGTGATGAAACAG	9873
rs529649812	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73073497	GTAATACAAGTTTAC[C/T]TTGCATGTGCTTGAG	9873
rs529655128	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72950582	CAATTTGTTGAAAGA[C/G]TATTCTTTCCTCCAC	9873
rs529661388	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108239	GATCTTTTGCCCATT[C/T]CTTAATCAGATTATT	9873
rs529670615	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73107650	CTCGAGTTCCATGAG[C/T]TCAAATGTTTTCATT	9873
rs529674731	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72989652	CCCCTGCCCAACTCC[A/G]TGGATACACATATAC	9873
rs529674886	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900165	TATACATGTATATAC[A/G]TAACTTTCATCCCAA	9873
rs529696717	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051997	CTGCAATAAAGAACC[A/C]ATTTCCAATGACACC	9873
rs529698035	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135410	AATTTTTCCATATTA[C/T]AGACCTCCTTAAACT	9873
rs529714697	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099682	CGTTAGGCTTAGCGG[C/T]GCTCACCACCCTGGT	9873
rs529720916	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951792	AGGTTTACCCTTTCA[A/C]AATCTCTTTATAAAT	9873
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	9873
rs529726555	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991086	ATACTATAAACACCT[C/T]TACGCAAATAAACTA	9873
rs529736368	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73044241	ATTATTGCCTCACTT[A/G]TTAACGCTGAATTCC	9873
rs529757456	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134846	GGGAGTTTGTTTTTT[C/G]GTTTTTGGTTTTTTT	9873
rs529758452	snp	A/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73052660	AGTTTGGTCCTAATG[A/T]TTTAAAGGTGTGAAT	9873
rs529768098	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72845658	CTGTGGGCCTCTTGA[C/T]GCTTTGGCCCCTGCA	9873
rs529775204	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73142901	GACGACGCTCGCAGG[A/G]AAACGTTTGCAGTGG	9873
rs529812643	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72886138	ACCTAAACCAGTGCA[A/G]GGATTCCTTGTATTG	9873
rs529817944	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73037957	AACTTATTTTATTTT[C/T]ATATGAAATATGTGA	9873
rs529827925	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936923	TAAGTCCAATGTATG[A/G]ACTTCCTTGGAGACA	9873
rs529829545	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944578	GAGAAGGAAATAAAG[A/G]GTATTTAATTAGGAA	9873
rs529837591	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73024184	AAAATCTACCAGTGG[C/T]TGGGGGAACCGAAGA	9873
rs529839579	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892229	TTATACCTTCTTATT[G/T]AGTATTCACTGTGCT	9873
rs529865650	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72937513	TTAATAAACATGTCA[C/T]GGACATATGGGACCA	9873
rs529881500	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72898728	ATTGCTTTTCTTTCT[-/A]TTTTTTTTTTTTTTT	9873
rs529885578	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142154	AGGAGGCGGAGACGG[C/T]GAGGGGGCGGGGGCC	9873
rs529889493	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73092784	CAAGCATTTTGTGTA[C/T]ATCAAATCAAGGAGG	9873
rs529898819	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72975798	AAATTATCAACTAGT[A/C]AATGTATGTTTGGCT	9873
rs529905272	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877237	TGTGATAAGCAACAG[C/G]TAAAATTTCTCCTGG	9873
rs529910197	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093694	ACAACCTCCGCCTCC[C/T]GGGTTCAAGCGATTC	9873
rs529920921	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085285	TAAGCAATGAGAGAG[G/T]ATTCTGGGAGATGGC	9873
rs529921261	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73138162	TGTGCCACATCTCAT[A/G]TGTATTGTCATTTGA	9873
rs529927877	snp	C/G/T			intron-variant	FCHSD2	GRCh38.p7	11:72915188	TGCAAATCAAAACCA[C/G/T]CATGAGATACCATCT	9873
rs529940416	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72878187	TGGAGGCTGAGGCAG[A/G]AGGATCATTTGAGTC	9873
rs529948606	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72865650	ACTATCTCAAATGAC[A/G]TATCCTCCATGGGGC	9873
rs529953102	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72984746	GGTCTAAATCTAAAC[G/T]AAATAGATTTTGTAG	9873
rs529957400	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72847018	ATTTATTTTTTAGAG[A/G]CAGGGTCTCACTCTG	9873
rs529959601	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72985897	GACCAGTGATTTTTT[C/T]TTTAAAGCTGCAATG	9873
rs529966875	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73036324	TAGGAAATAAAAGAC[-/A]AAAAAAAAAAAACCC	9873
rs529972572	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73128965	CAACCTCCATCTCCC[A/G]GGTTCAAGCGATTCT	9873
rs529979603	snp	G/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73112072	TTTCTGTGTACTTAC[G/T]ATTACCAGTGAGTTT	9873
rs529990484	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73076442	AAGAAGACAGACAAG[A/G]AAGGAGACATACCAT	9873
rs529991049	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869404	GAAAGGGAGGGGAGA[C/T]AGTGAAGAAGGGAAA	9873
rs530008100	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024359	TATTTTAGCTAGAAA[C/G]TGTACGACTAAAGAC	9873
rs530010230	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914140	CTGCCTCAGCCTCCC[A/G]AGCAGCTGGGACTAC	9873
rs530045089	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976630	AGAAAACTGGAGGAA[C/T]CACATTACCTAACTT	9873
rs530059669	in-del	-/GGGGCGC	0.0232847	0.105357	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73142874	GTGTGTGTGTGTCGG[-/GGGGCGC]GGGGCGCGGGGGACG	9873
rs530073736	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016400	TACAACCTTTTTTCA[C/T]TATTGTCCAGTCCTC	9873
rs530074571	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861437	GATAACAGCCCTGGT[A/G]AATTCCACTAAACAT	9873
rs530075772	in-del	-/TAC			intron-variant	FCHSD2	GRCh38.p7	11:72872667	TCTATTGTATGGATA[-/TAC]ATTAGAATGTTTATC	9873
rs530080204	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72875874	CTTCTTGAAATATGC[G/T]GCCACCATGCTGGGG	9873
rs530089767	snp	A/G	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:72956316	AGAAAACCACCATTT[A/G]GCAACCATCATAAAG	9873
rs530090539	in-del	-/T	0.148661	0.22854	intron-variant	FCHSD2	GRCh38.p7	11:72959395	CACCATGCCCGGCTA[-/T]TTTTTTTTTTTTTGT	9873
rs530097851	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061518	GTGGTATGGGTCTGC[A/G]GGTCCCACCCCCACG	9873
rs530130353	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862036	TGCAATTACACCATA[A/T]TAGCAGACTAAAAAA	9873
rs530135705	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008760	AAAGATATAAAGATA[C/T]AGTTTGTGTCATTAT	9873
rs530137764	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72952637	GCCTATAGTTAATTT[G/T]GGTAAGAAAATTTGG	9873
rs530161988	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72909200	CGCCGCCACGCCTGA[A/C]TGGTTTTTGTATTTT	9873
rs530185133	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960172	GTCATAGTGGAAGGC[A/G]AAGGCAGAGCAGGCA	9873
rs530209355	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73017034	AATGCCCAGGCTGGA[A/G]TGCAGTGGCGCGATC	9873
rs530212518	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108911	GATTTGGTTTTTATA[C/T]ATGGCAAGAGACATG	9873
rs530214819	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72944719	TCAGGATACAAAATC[A/G]ATGTGCAAAAATCAC	9873
rs530215148	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73054733	CAGGCTGAAGTGCAG[C/T]GGCACAATCATGGCT	9873
rs530216552	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72906733	AAGATCAGATGGTTG[C/T]AGGTGTGTGGTGTTA	9873
rs530219838	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945506	AAGGACTTCATGTCT[A/G]AAACACCAAAAGCAA	9873
rs530222774	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961038	TGGGGAGGTAACACA[A/C]ATGTGAGGCTGCCTT	9873
rs530224098	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72927831	GCACCAATAGGTACT[G/T]TTACTGTAGATGGAT	9873
rs530234408	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062154	AGCCTCTGCTGATGA[C/T]ACCCAGGCAAACAGG	9873
rs530273102	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045877	ACATATGTAACTAAC[C/T]TGCACAATGTGCACA	9873
rs530278538	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000485	GTCCATTTGAAAACA[C/T]TTACTCATGTGTAAC	9873
rs530297332	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73088397	ACAATGACGAAATTG[C/T]CTAACAATGCACTTC	9873
rs530313484	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73133971	AACATTTTAAATTGG[C/T]GTGACGATTGTACAA	9873
rs530318057	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854898	ATCCCAGCACTTTGG[A/G]AGGCCGAGGCAGGCA	9873
rs530318094	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846593	TTAGGGACTACATTT[C/G]TTCTCACTTACCCCA	9873
rs530323095	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73054793	TGATCCCCCCCACCT[C/T]GGCCTCTAGAGTAGC	9873
rs530329603	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847452	GGGCTGAAGACACAC[A/G]GACAAGGTAAACATA	9873
rs530341485	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939303	ATTCCCCCCTAAAAA[C/T]TGTAACTAAGCATTT	9873
rs530342350	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72945989	GGAAGTCAGTGTGGC[A/G]ATTCCTCAGGGATCT	9873
rs530360358	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73060893	TAGCTTGAAACCAGG[C/T]ACTATAGTGAGATTC	9873
rs530371545	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087043	CTTCAGGAGGTATAC[A/C]AGAAAAAGGCATTGT	9873
rs530372220	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894581	GTATATTAATATATG[A/G]TTAATTATTTCAATA	9873
rs530381501	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72883854	GGAGAATCGCTTGAG[A/C]CCAGGAGGTTCGGGC	9873
rs530389554	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916817	ATCTATGTTTTCTTT[A/C/T]GTTACTTGTGCTTTC	9873
rs530390817	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72926725	CAGGACAAGAACTTG[C/G]GCAAAGGCACCATGG	9873
rs530393612	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73027708	GTTCGCTGCACTCCC[C/T]GCCATCACAGGCCCA	9873
rs530402079	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73103157	AATGTTCTATATATT[G/T]AGTGTAGTAGTGTTT	9873
rs530404099	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72993946	TCGGATAGAAAAGCC[A/C]GGCTTTGGGCTTCTG	9873
rs530412936	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72873696	TTTTTTGTAAGTTTA[C/T]TAGCTTTCGCTGTTA	9873
rs530418260	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126069	TTCCACGGCCAGGTG[A/C]GGTGGCTCACACCTG	9873
rs530425832	snp	G/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72917340	ACCTTTTTCTGAAGA[G/T]AATATTCTTTCTCTA	9873
rs530437541	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140913	TGGGGGTACATGTTC[G/T]AAAGAAAAGGACTCA	9873
rs530445753	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085998	GGTTTTAAAGATGTT[C/G]AAAGAATTAAAGGGC	9873
rs530468271	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73095856	AAAAGATAGTGAGAG[A/T]GCCTACACTATGAAC	9873
rs530473700	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142069	AGAGAGCGAGTGTGA[A/G]GAGACGAGGGAGGAG	9873
rs530477130	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72862633	TTGGAAAACTGAATA[C/T]TGTTAACATGGCAAT	9873
rs530478897	in-del	-/A	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72930683	TGGGAGGGAGGCTAC[-/A]AGTAAGCCAAAATCG	9873
rs530479221	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864617	ATTAAAAAATAAATA[A/C]ATAAGAGTAAGGAAA	9873
rs530496726	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129472	AGATTCTCATGGCAC[A/G]AACCCTATTGTGAAC	9873
rs530498461	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971440	CAAAAGGGAGATTAT[C/T]TGCGATTACCTAATC	9873
rs530520998	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134718	AAGTGTCTTTGACTT[C/T]GGTGAAACTCACGTT	9873
rs530523085	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73072394	TTCTTTAATGAAGTT[C/T]AAAAACTTAATTAAA	9873
rs530531293	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73070706	GCTGGTATTACAGGC[A/G]TGAGCCACCATACCC	9873
rs530544861	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72915681	AAATTAGCCGGGCGC[A/G]GTGGTGGGCGCCTAT	9873
rs530549362	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73065564	AAGAGAGGAAGTCAA[A/G]TTGTCTCTGTTTGCA	9873
rs530558686	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72880869	GATACCCTGTCTCGA[-/A]AAAAAAAAAAAAGAA	9873
rs530565055	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73019901	ATAAACCTATGTCTT[A/G]CAATTTTTTAAAGTT	9873
rs530567340	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72867768	CTAGCAAACTATTAT[C/G]TTTTTAAAAAATTTT	9873
rs530600536	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73038509	TACAGCGTGGATACT[A/G]TGCAGCCATGAAAAG	9873
rs530609119	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72948740	GCACAATCTCGGCTC[A/C]CTGCAAGCTCCATCT	9873
rs530612461	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058149	CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC	9873
rs530631090	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72964915	CTGCCTCAGCCTCCC[A/G]AGTAGCGGGGACTAC	9873
rs530632717	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72955882	ATATTACAGTGCATA[C/T]ATACATATATTTCCT	9873
rs530633398	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72850707	TCAAATATGTAAGAA[A/T]TATTTATCAGTATCC	9873
rs530655072	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905316	AGTAGGTATTTATAT[A/T]TATGGGGTACATAAG	9873
rs530659981	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857406	ATACTAACGTTTACC[C/T]TTTCTTAGATGTTGT	9873
rs530661826	in-del	-/TAA	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72923950	TCTCAGAAAATAAAT[-/TAA]AAATAAATAAAGTTG	9873
rs530667443	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897917	TTTCTAGAAAGAGCT[A/C]TGGCTTTCTGGTATC	9873
rs530729838	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850107	TCGCTCTTGTCACCC[C/T]GGCTGGACTGCAATG	9873
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	9873
rs530746943	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004492	TATAAGAACCCACAA[C/T]CCATTTGGTCCTACC	9873
rs530751770	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118428	ACCAGAGGAAACCAC[C/T]GTACTGACTTCTCCA	9873
rs530752410	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897187	TCTGACTCAATGTGC[C/T]AGGCATTGAGTTAAA	9873
rs530753029	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980577	TAAGCAATAAAAAAG[A/T]TAGCTATTATTATTA	9873
rs530754918	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73105749	AATAAATTCAAATTA[C/T]ACTAATTATTTTTAA	9873
rs530776593	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943119	TCCTTGGCCTCCTGA[A/G]TAGCTAGGATTACAG	9873
rs530794585	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043117	GGTGAAAGTGGGCAT[A/C]CTTGTCTTACTCCAC	9873
rs530818805	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098341	TGTTTAATTTCTACA[C/T]ATTTGCATATTTTCT	9873
rs530825350	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091563	CAAAAAAAAGAAAAA[A/T]GAAAAGAAAGCAAAT	9873
rs530828158	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72990248	CTAGATCTGTGTTTC[A/G]ATAGAAACCTGATGA	9873
rs530840345	snp	C/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843054	ATTATAGGACAGGAG[C/G]AAAGTTGTGCTTTTT	9873
rs530853904	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042420	CCATTGTTCTATGTG[C/T]CTGTATTTATATCAA	9873
rs530854343	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036016	GAGCCACCACTCCTC[A/G]CCCAGTTTTTATTAA	9873
rs530861672	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72935922	CTACTAGCATGCAAG[A/G]TAAGTCAGATGTCTG	9873
rs530862263	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982092	TGTCTCTATATTTTC[C/T]AACCTGTATTCTAAT	9873
rs530865223	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889484	TACAGAAAAAACACA[G/T]ATAATGCTTGAGCAA	9873
rs530866888	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73131594	CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC	9873
rs530873021	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997794	CAATCTCTACCTCCT[A/G]TGCTCAAGTGATCCT	9873
rs530875272	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72928908	CCCCGATGTGTGATG[C/T]TCCCCTTCCTGTGTC	9873
rs530875318	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72996891	TAAGTCTTAAATTCA[A/G]CTTAATGTTTTTCCT	9873
rs530879197	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117161	TTATAACAAATACAT[C/T]CTACATGTACTAACA	9873
rs530901674	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72846291	TTCAAGAAATTCTCC[-/T]TGCCTCAGCCTCCCA	9873
rs530918101	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73035356	TATTTTTTGTAGAGA[C/T]GGGGGTCTCATCATG	9873
rs530920354	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73064477	CAAGAAAAACCCTTC[-/A]AAAAAAAAAATCAAT	9873
rs530939542	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73124438	AAAAAAGAAGAGAGA[A/G]AATGGGGCAGAAAAA	9873
rs530947906	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084308	AAAACAATGTACAAG[A/G]CCACTACAAATTGTG	9873
rs530949651	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73120612	TGCATGCCTATAATC[C/T]CAGCTACTCAGGAGG	9873
rs530952024	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981318	AAGACTTCAAAGTAA[A/G]TTCGAGAACATATAT	9873
rs530955365	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72973552	CAGGGCATGATACTA[C/T]CTAAGACAACACTAT	9873
rs530958424	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72880353	AAGCTGGAGGTAATA[C/T]ACTACCTGACTTTAG	9873
rs530984556	in-del	-/TAAAATAAAATAAAA	0.00322906	0.0401001	intron-variant	FCHSD2	GRCh38.p7	11:73080973	CAAAAATAAAATAAA[-/TAAAATAAAATAAAA]ATAAAATAAAATAAA	9873
rs530991529	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882727	GCCTAAATAAATAGA[A/G]AGACACATCATGTTC	9873
rs531000753	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875174	ATGTATTACTATTTA[C/G]GACAGTGGTTTACTT	9873
rs531008117	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075237	AATCACCTGAGAAAA[C/G]CATTTCATGATATTT	9873
rs531019705	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72911563	TGCATTGAATCTGTA[A/G]ACTGCTTTGGGTAGT	9873
rs531031385	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72859126	AGTATAGCAGTCTCC[C/G]CTTATGTGTGGTTTG	9873
rs531051039	snp	C/G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73048270	CCTCAGCTCATGCCA[C/G/T]GTACCGACACACATA	9873
rs531060082	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73133018	GCACATGAAAAAATG[C/T]TCACCATCATAAGTT	9873
rs531069723	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067032	ATAAAGACACATGCA[C/T]ACGTATGTTTATTCC	9873
rs531076341	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966253	CAACCTCTGCCTCCC[A/G]GGTTCATGCAATTCT	9873
rs531095681	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73029468	GCTCAGCTGTGGCTA[A/C]CCATCTTTATCCCTG	9873
rs531097502	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021796	CTAATAACGGATATA[C/T]ACAAAAAACTGGCTG	9873
rs531112625	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958622	TTCAATATTTTCCTA[G/T]ACTGATCCATCAGTT	9873
rs531128109	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066542	CAAAAGAAACTATCA[C/T]CAGAGTGAACAGGCA	9873
rs531129217	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73028467	ACCCCCATTGTATCT[G/T]GGAAGTAACTAACTT	9873
rs531131571	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72912996	GGACACTTACAATCA[C/T]GGCAGAAGGCAAAGG	9873
rs531136975	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920643	CATAGAAGGAACAAA[A/G]ATAAGATTTTTTCAT	9873
rs531145710	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851624	GGCATGCGCCTGTAG[A/T]CCCAGCTACTTGGGA	9873
rs531157990	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72868134	CTGGATAAAGAAAAT[A/G]TGGTACATATACACC	9873
rs531161448	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022618	GGATGGAGAGACATT[C/T]CATGTTAATGACTTG	9873
rs531170510	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014264	AGCCTCCTGAGTAGC[C/T]GGGACTACATGCACG	9873
rs531200165	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72957840	AAGCACATAAATATA[C/T]AGTGAGGGAGAGGGA	9873
rs531211425	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114887	TGTGCGCCCAAAACT[A/G]AGGGAGGGGTGGCAC	9873
rs531216742	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73024737	AAATACTGCAAACTA[C/T]GCATCCCACAAAGGT	9873
rs531218833	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913477	TTTCGCCATGTTGGC[C/G]AGGCTGATCGCGAAC	9873
rs531221546	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73094735	GTGCTTTTATTATCA[G/T]CAAATTGATAATTGT	9873
rs531225841	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72906689	AAACTGAATCCTTTC[C/T]CCATTTCTTGTTTTT	9873
rs531250629	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73103346	ACTACTTCAGAACCC[A/G]CAAAACACTGAAATA	9873
rs531254495	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138872	CTCAGCCTGCCAAAG[A/T]GCTGGGATTACAGGT	9873
rs531255201	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930894	ACAATAGGGTGACTA[C/T]AGTCAATAATAATTG	9873
rs531269701	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73047971	ATTATGTTAACAAAT[A/G]GTGGAGCCATAATTA	9873
rs531275192	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121529	CCTATACAAATAATG[A/G]TATCTGCCTCTTGGG	9873
rs531286618	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73055139	AAACCATCAGATCTC[A/G]AAAGAACTCACTATC	9873
rs531288624	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73102229	TTAACAATTCCAAGT[A/G]CTGATAAGGATTTGG	9873
rs531320337	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118117	AGGTCACGCATTCCC[A/G]AGACCAGCCTGGCCA	9873
rs531321332	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73045783	TGGGGTGGGGGGAGC[A/G]GGGAGGGATAGCATT	9873
rs531337730	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73129802	CAAAAAGGGTTGGGG[A/G]CCACTGCTGTAAACT	9873
rs531344404	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73087666	GCCGAGATCACACCA[A/C]TGCACTCCAGCCTGG	9873
rs531347471	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73078782	GAAGCACAGTGGTGC[A/G]ATCACAGCTCACTGC	9873
rs531350393	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977680	TCAGGAAACAACAGG[C/T]GCTGGAGAGGATGTG	9873
rs531371695	in-del	-/TATG	0.23482	0.249539	intron-variant	FCHSD2	GRCh38.p7	11:73025996	GAGATTCATTTTATG[-/TATG]TATGTATGTATGTAT	9873
rs531376554	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73068123	CCACCAGGTCCCTCG[A/C]ACAACACATGGGAAT	9873
rs531379271	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73025231	TAGAAAAGACATGGA[A/G]TCAACCTAAACGCCC	9873
rs531379983	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031728	GCCAGTCCACACTCC[C/T]GTTATTCTATTTCTC	9873
rs531382728	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72939047	ATACAGTAGCCAAAC[C/T]GTACTTTTTTGGGGG	9873
rs531385725	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969228	AAACCTTATGAGAGA[C/T]GGAGCTGCATTCCAA	9873
rs531393131	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72986165	TGGGTTTAAAAGATT[C/T]CTGTTATTTTTTACC	9873
rs531411596	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73070235	AGTCTATTTCATAAG[G/T]CTATTTCTAACAAGC	9873
rs531437758	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73017123	AAGTACCTGGGACTA[A/C]AGGCACATGCCACTG	9873
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	9873
rs531445690	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032518	GGTGTGAGCCACCAT[G/T]CTTGGCCTATTTCTA	9873
rs531461546	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73082065	AAAATCGGCTGGGCG[C/T]GGTGGCTCATGCCTG	9873
rs531473381	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969677	GTATGTTTTGACTAG[A/T]TAATTTAATAAGAAA	9873
rs531478343	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862996	AGCACAATCATAGTT[C/T]GCTGTAACCTTGAAC	9873
rs531478548	snp	G/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72961405	ATTTTTAAGAAGTTT[G/T]TTGTTGTTGTTGTTG	9873
rs531500657	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923977	GTTGTCTTTTTGTTG[A/T]TGGGTTGTAAGAATC	9873
rs531524554	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73129122	TTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	9873
rs531527807	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137207	TCTTTGAAAAAAAAA[A/C]GCAAATCAGAAACCT	9873
rs531537505	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73079389	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	9873
rs531538206	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915679	AAAAATTAGCCGGGC[A/G]CGGTGGTGGGCGCCT	9873
rs531538252	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72924408	GCAGCCTCCCGAGTA[A/G]CTGGGACTACAGGTG	9873
rs531538936	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73020457	TACTATACCATTTTG[G/T]CATGAAATTCCCGGC	9873
rs531539126	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863560	TAAGGAAATAAAAAA[A/C]TAAGCCACAGACTAG	9873
rs531539287	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855013	GCACGGTGGCTCACA[C/T]CTGTAATCCCTGCAC	9873
rs531550134	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855733	GAGTGTAAAAAATGA[C/G]TTAGATCCACAGGCA	9873
rs531567343	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110380	TTATTTGTTATTGCT[C/G]TGTTCAGGTTTTGGA	9873
rs531599373	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923075	CCTGGCTTCTGTTGC[A/C]CAGCATAATATTTTC	9873
rs531603698	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062251	AACAAACAGAAAGGA[A/G]TAGCATGTGCACTCA	9873
rs531610909	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72982229	CCTTCAACACTCTTG[-/T]TTTTGCCTGAAGGTC	9873
rs531617918	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002174	GACAGTGTAGAAGCA[A/G]GAAAAAGAAAAATTG	9873
rs531618304	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841760	AAGCTCCAATTTTGC[A/G]TTGCACTTCACTTTT	9873
rs531629959	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010843	TGGCTTACTCAGATG[C/T]TGGTAGTGGCAGCAG	9873
rs531630236	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73103426	TAAGATTTAATTAGA[C/T]TTAGTTTAGGTATCC	9873
rs531644993	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895575	AGCACATAACTAATG[C/T]GTCTATGCAAAGATC	9873
rs531646161	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72954921	ACAGATCTGGCTGTA[C/T]GTATATGTAATAAAG	9873
rs531663490	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909724	CGCCTCTGCCTGGCC[A/G]CCACCCCGTCTGGTA	9873
rs531667401	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062868	GAAAACACACTTCAG[C/T]GTATTATCCAGGAGA	9873
rs531667620	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72904070	ATACACCACGGAGTG[C/T]GTAAAGGGTACGAGA	9873
rs531692671	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73130626	ACCAAGAGTCACCAA[C/T]AGGAAGAGGTATTAC	9873
rs531715447	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143131	GCACTCTACTGCAGG[A/G]CATTCAAGTCAAACA	9873
rs531727802	snp	A/C/G	0.00677183	0.0578675	intron-variant	FCHSD2	GRCh38.p7	11:73063695	AAAGAGACAAAGAAC[A/C/G]GTATTACATATTGGT	9873
rs531728829	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72887416	AGATGTATATCACAG[C/T]TGTGACAGTGTCATT	9873
rs531729233	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72954267	CTGGAGTGCAGTGGC[A/G]CAGCATGGCGGCTCA	9873
rs531738325	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848932	ATCAAAACGATTTAC[A/T]TTGGAAAAAAATGCT	9873
rs531745747	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848341	TCTCATCACACTCTG[A/T]CTCTATACCTGCTGT	9873
rs531749373	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903472	GATCCACCGGCCTCG[A/G]CCTCCTAAAGTGCTG	9873
rs531749650	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72973109	CGCGGTGGCTCATGC[C/T]TATAATCCCAGCACC	9873
rs531766735	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72888205	AAAAATCTAGGTATG[A/G]CCAGAAAGGCAGAAG	9873
rs531774543	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946836	GTTAAGTATAATGCC[C/T]AGGGAAATTTTTCAA	9873
rs531778294	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72975655	TTATTATGTATCAAT[A/T]TTAGAAAGGATTTGT	9873
rs531799864	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73078164	TATATACTCACCAAA[A/C]TGTCAGTCTTTTTAA	9873
rs531815455	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73003807	ATATGAAGCAATTGT[C/G]AAGGATAAGAAAAGT	9873
rs531823151	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73097086	CAGCTCACTGCAGCC[G/T]CGACCTCCCAGGCTC	9873
rs531827881	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096105	CGAGGTATCTAAACA[C/G]ACGTAAAATTTTTAA	9873
rs531853027	snp	A/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73047646	TAACGGCAAATATTT[A/T]TGCTCTTTCTTTCAG	9873
rs531854590	in-del	-/AAACAAAC	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72868691	GCAAGACTCTGTTAA[-/AAACAAAC]AAACAAACAAACAAA	9873
rs531857195	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041836	AAATTTTTGCCTAGG[C/T]CAATGTCCTGGAGTA	9873
rs531859118	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840601	TAGCCCGCTTTAATG[C/T]TCATAAAGTTTGTTC	9873
rs531866943	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988376	CCAGTTCCTTCTTTT[C/T]CTACTTATTCTTAAA	9873
rs531872755	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72904028	TAATCTGGGAACTGG[A/G]CGAACCAAACAGACT	9873
rs531873030	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73015694	AATTATATCCGAAAA[C/T]ACAGCAGAGGAAAGA	9873
rs531875192	snp	A/G	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:73127547	AGATCACCCCTGAAG[A/G]CTGATACCAACAACA	9873
rs531877770	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72995102	TTATGTTTCTCACTT[C/G]TTTCACTTATCAAAA	9873
rs531880028	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73008757	TACAAAGATATAAAG[-/A]TATAGTTTGTGTCAT	9873
rs531881463	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73096559	AAGGAAAGGAAAGGA[A/C]AGGACAGGACAGGAT	9873
rs531881973	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112845	CTTATTTAGTATTTT[C/T]AGTAGAGATGGGGTT	9873
rs531882740	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080756	CAAAACCAGCCTGGA[C/T]AACATTGTGAAACCC	9873
rs531886856	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73110806	GATGTAGGTACTTAT[A/C]GCTATGAACTTCCCA	9873
rs531890579	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034724	CTTATTTGCACAAAA[C/T]GACCTGCAAATTTTA	9873
rs531890724	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027226	ACCATTGATCACTGA[C/T]AGTGATATGGGCAAT	9873
rs531900607	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72940702	ATTCATGTTCACCGT[G/T]GTGGCAGAAAACGCC	9873
rs531913648	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881203	ATGTAATCTTATTAA[A/G]AATTGGGCAATGGAT	9873
rs531918603	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041068	CAGAATTTCATTCTT[C/T]TTTATGGCTAAATAG	9873
rs531920668	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73114929	CGGACGCCATGGCTG[C/G]TGTCTCACTAGGTCA	9873
rs531944254	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119753	TACCTGGCCTAGACA[A/G]CCATTTAAAGAGTAT	9873
rs531946103	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73112249	ATGTTTGAAGGATAT[C/T]TTCACCAGACATACC	9873
rs531982335	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72912771	GCTTTTCCTTGCTGA[C/G]AGACTTTCTATTACA	9873
rs531998128	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72979866	CAGAGGGCAACTAGT[A/C]CAGATTAGAAGAATG	9873
rs532002504	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72952394	CAGTGGCACTATTTC[A/G]GCTCACTGCAACTTC	9873
rs532008935	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73119296	CAACAGAGCGAGACT[C/T]TGCCTCAAAAAAAAA	9873
rs532015360	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73089326	TCAGAACTCTCATAG[C/T]GTTAGTGGAAAAGTA	9873
rs532019916	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72906495	TTAGTCATGAAGTCT[C/T]TGCCCATGCCTATGT	9873
rs532036057	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73023698	AAAACTTAGGTTCAC[-/A]AAAAAAACCTGAGCA	9873
rs532038989	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129058	TTGTATTTTTAGTAG[A/C]GACGAGATTTCACCA	9873
rs532041123	snp	A/C	0.000633692	0.0177889	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842583	GGAGCAATTTTCTTT[A/C]AACATCTTTTAATTC	9873
rs532056725	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006337	AAATTCTTGATTTCC[C/T]TAAAATCTGTTCTGG	9873
rs532075125	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898901	TGCCCAGCTAGTTTT[C/G]TGTATTATTATTATT	9873
rs532084552	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970811	ATTTTGGGGTTAGGT[A/T]TACAAAATGGGACAA	9873
rs532111771	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72899693	GTGAGCCGTGATTAT[A/G]CCATTGCACTTCAGT	9873
rs532123067	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051842	TTTTTATATAATAGA[C/T]CTTCAGGATGCTAAC	9873
rs532131127	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73136321	TCTCAAGCTGGGCAC[A/G]GTGGCCTGACGGTAG	9873
rs532134813	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059065	TTGTTGAACTGTACT[A/C]AATTCAACAAACATG	9873
rs532151718	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72998662	TAAAAGAATATAGGA[C/T]TTAAAAAGTAAGAAG	9873
rs532156469	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73124093	CCATAAAAAAGGATG[C/T]GTTCACGTCCTTTGT	9873
rs532164440	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73099713	TCTTCTGCACCCTCG[G/T]TCTGGTTGGGGCTGT	9873
rs532185611	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051231	GAGGAGGGAAAATCA[A/G]TTGAACCCAGGGGAT	9873
rs532189122	in-del	-/TT	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73121159	GTCTCACTCTCTCTC[-/TT]ATACACATACACATA	9873
rs532197272	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890936	AAGAGGCTTTTAATA[C/T]AGAAAGCAGCAAAAT	9873
rs532201423	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73131978	ATCAGTCACTGACAT[C/G]CATATATTTCCACAA	9873
rs532212130	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991005	GAAGAATCAAACAGA[C/T]GCAATAAAAAATGAT	9873
rs532215122	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998056	TAATAAACTTGTTAA[A/T]TATTCAGATTGAAGT	9873
rs532216436	in-del	-/A	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73048294	ACACATATGGGACCC[-/A]AAAGTTACCTCTGAT	9873
rs532221007	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037189	ACAGAGAGTTCCCAT[C/G]TATCACTTGCCCCCA	9873
rs532229523	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907310	TTACTCTTTTCCTAA[C/T]TGAATACCCTTTATT	9873
rs532252822	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72936919	CTAGTAAGTCCAATG[C/T]ATGGACTTCCTTGGA	9873
rs532254077	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943360	CTTAATTCAACTATA[A/G]TTAGGATTAACTGAG	9873
rs532255997	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043305	TTAAATCACTAAAAG[G/T]CTCGGTCAAGTAGTG	9873
rs532264528	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951053	GACACAGGTTTAGCC[A/G]GGCCATGAGAGAAAG	9873
rs532267928	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72949800	ATTTGGGTTGTTTCC[A/G]CCTTTGGATTGTTAT	9873
rs532279197	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73051534	TGTCTCTGAATGAGG[C/T]AGAGGTAGTAAACCA	9873
rs532284655	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72929184	GCCGCTATAAACATA[C/T]GTGTGCGTGTGTCTT	9873
rs532286163	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029752	CCACCTTTTGAGAAC[C/T]ACACATTGAAAATTA	9873
rs532286213	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037784	TAGGAGTCCTCATTA[C/T]CTTGTAACCCTCCAA	9873
rs532300823	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909805	TCTGCCCGGCCGCCC[C/T]GTCTGAGAAGTGAGG	9873
rs532321028	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928463	TCCCAAATAAGTTAT[A/T]CTCTTGGCCTAGAAT	9873
rs532321128	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142190	AGCAGGGGCGCGAGG[A/G]TCTCAGCCGGCCGGG	9873
rs532324640	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135624	AAGAAAGTAGACTCT[A/G]CTTGTCTACTGCTGA	9873
rs532326716	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72844777	AACTCCAAGTTACAC[A/G]AACAAAAATAAGGCA	9873
rs532339581	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920876	GATTTTTGTATTTCC[A/G]TATCAACCTAGCATT	9873
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	9873
rs532360674	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72883057	AGGTAATGGGAAAAG[C/T]ATACTCTTTAAAATA	9873
rs532363635	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092288	GTACACCACCACACC[C/T]GGCTAATTTTTTAAG	9873
rs532369397	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72911726	ACATGTGCACAATGT[G/T]CAGGTTAGTTACATA	9873
rs532403832	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869896	AGTTTAAAAACTTTC[A/G]TAACTCCTGACTGTC	9873
rs532405717	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983020	AAGAAAGGGGCCGGG[C/T]GCGGTGGCTCATGCC	9873
rs532432702	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72904512	CAATATTCTTTCATC[C/T]TTAAGCCCACCTACC	9873
rs532436870	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023552	ATGCTAGTGAGGACG[C/G]AGAGTTACAGAGTAC	9873
rs532468809	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72967462	ATTACTAATATATGC[C/T]ACAACATGAATGAAC	9873
rs532479174	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075470	GAACTAGAACCTTCA[G/T]GCATTGCAAAACGAG	9873
rs532483588	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72884321	GATGTTAGGAAATAC[A/T]TGTTTATTCTTCATA	9873
rs532495339	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73015703	CGAAAACACAGCAGA[A/G]GAAAGAAGTAATTCT	9873
rs532504465	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72929953	GAAGGGTCTGAGCTA[C/T]AAAAGCAGACTCCAG	9873
rs532510595	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023010	ACAACAAAACAACAA[A/G]AACCCTTGACACATA	9873
rs532523149	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72877185	AGAGATGGGGTTTTG[C/T]CACTTCAGTTTTTTT	9873
rs532530828	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112302	CTTTGGCACTTTAAA[C/T]ATGTCATGTCACTCT	9873
rs532534938	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72975600	CCTTACACATTGTAC[A/G]CATGCATCAAAATAT	9873
rs532544135	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913761	TTTCAACAGTCAAGC[C/T]GAGAGCCAAATTACT	9873
rs532548262	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72853326	AAATCTCACCTTATA[C/T]GATACACAGAAAAAA	9873
rs532549331	snp	A/G	0.000475384	0.0154099	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841601	GCAGCAAAGGGAAGC[A/G]AGGTTACCCGGTGCT	9873
rs532559076	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061460	CCAGTGAGACAGAAC[A/G]ATTCACTTCCCCTGG	9873
rs532565385	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951959	TCTTTCACTTACAAG[A/G]TAACTTTCAGAATCT	9873
rs532576441	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72898683	TTCTGGCTCTAATGC[C/T]TATTAGCTGAGTGAC	9873
rs532594097	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72889252	AGGCGTGAGCCACCG[C/T]GCCCGGCTATAATTA	9873
rs532595495	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118682	TGATTTCTATTTTCA[C/T]TGCATGTGATCAGAG	9873
rs532605776	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73048588	TTTCATTCTGGGACC[C/T]CATCTGAAGTAGTTA	9873
rs532605809	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72944869	GACCTCTTCAAGGAG[A/C]ACTACAAACCACTGC	9873
rs532611203	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900850	TAAACTCTGGAACTA[C/T]ATCATAAACTCCCTT	9873
rs532636253	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024179	TAAAAAAAATCTACC[A/G]GTGGTTGGGGGAACC	9873
rs532646530	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967893	TCAGGAGATTGAGAC[C/T]ATCCTGGCTAACGCG	9873
rs532681104	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73101491	GTCACCTAGGCTGGA[C/G]TGCAGTGGTATGATC	9873
rs532688795	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119218	GAAGAGGGAAGATTG[C/T]TTTGAGTCTGGGAGG	9873
rs532690060	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945468	AAAAGCTAGGCAATA[C/T]CATTCAGGACATAGG	9873
rs532693093	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72861087	TAGAAAAGAGAAAAA[C/T]GAGGGAAAAATCAAT	9873
rs532701254	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108374	TCTTCACTTTGTTGA[C/T]TGTTTCCTTTGCTGT	9873
rs532704645	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72861989	GGTTTACCAGGAATG[G/T]GAAGCTGGTTTAATA	9873
rs532712637	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73007745	TGCACAGAACTCAAT[A/G]TGCACACACATACAC	9873
rs532715976	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045175	TGAAAAAATGCTCAT[C/G]ATCACTGGCCATCAG	9873
rs532716225	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73093806	GACAGGGTTCTTCCA[C/T]GTTGGTCAGGCTGAT	9873
rs532731599	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052901	GCCCAGACTGGAGAG[C/T]AGTGGTGTGGTGTCA	9873
rs532737797	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72992907	GCCAAAATTGACAAA[A/T]AGGATCTAATTAAAC	9873
rs532750173	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126855	CCAGCCTGACCAACA[G/T]GGCAAAACCCTATCT	9873
rs532751127	in-del	-/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72866271	TTTTGTTTTGTTTTG[-/T]TTTTTTTTGTTTTTT	9873
rs532757633	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73026301	TAAATGAAATATTCT[G/T]TATGAGGACTATAGT	9873
rs532762898	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73085581	ACGCAACCACATTTA[A/C]GGGAGAAATTGAAAA	9873
rs532773028	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72999468	GGAACTACAGGTGCA[C/T]GCCACCACACCTGGC	9873
rs532775042	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008497	ACAGAAATAAAGACA[A/G]GGAAAAAGACTGCTT	9873
rs532777737	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969903	ACCTGACCCTCATTA[C/T]TACAGGAATAGGGGA	9873
rs532793153	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901602	CAGTGCACAGCACTG[C/G]AAATGTAGTAAGTGA	9873
rs532808642	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925500	CACTGCACCCCAGCC[C/T]GGGCAACAGAGCGAG	9873
rs532816971	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73125934	AACTACATTTCACAA[C/T]AGAAACAATGTTTTA	9873
rs532833994	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72916133	CTTAATACGTGGGTG[A/G]TAAAATAATGTGTAC	9873
rs532837551	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000309	ACTTCCACAAGAAAA[C/T]TTTAATTACTTATTA	9873
rs532855468	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054566	AATCTGGAAGACCCT[A/G]AAGAATCCCAGACAC	9873
rs532863624	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134055	ATGATATACAGTCAC[A/T]TCATGTAACTTACAT	9873
rs532865645	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846426	ACCTCGCGATTCGCC[C/T]GCCTTGGCCCCGCAA	9873
rs532878992	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73061494	GGGGTGCTGAAGCCA[A/G]GGAGCCAAGTGGTAT	9873
rs532891586	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072350	AATCTATGTCCCCAA[A/G]AGTACTAACATTTAA	9873
rs532897471	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116393	GGCATCACAGTTATA[A/C]AAGATTAATAAAATG	9873
rs532906827	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033797	GTATTCTTGGATAAG[A/G]CACCAAGCTAACTAG	9873
rs532938778	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019790	TGCTTAAATTAACTG[A/G]TTTCCTCTATACTTT	9873
rs532947045	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73111274	TAGCTCTAATATTTG[C/T]TTTACATATCTGGGT	9873
rs532949265	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064654	TTATATCAGTGGTGA[C/T]ATCCTGTGGGATATT	9873
rs532986924	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72864854	GCTGATGGGGTTGCT[C/G]GCAGCAATCTAACAG	9873
rs532986931	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73035254	TTGGAGCGCAGTGGC[A/G]CGATCTTGGCTCACT	9873
rs532993695	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72955660	TCTCCTATGACCCAG[A/G]AAACTCCAAGGGATT	9873
rs532999070	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002887	ATGTAATTGTTTATT[A/G]ACATCTGTCCCTCTC	9873
rs533016520	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73070467	CTCGTTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG	9873
rs533020945	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72970687	CTGCCACAGCCTGCC[A/G]ACATCCCACTCACAT	9873
rs533025944	in-del	-/ATTAA	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72972191	TCTCCAGCCCAAGAC[-/ATTAA]ATTAAACTCTGAAAT	9873
rs533028967	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72916711	TCAGATATGTGATGT[A/G]CAAATATTTTCTCTC	9873
rs533039155	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898596	AAAACTCAAAAATAA[A/C]ACCTGGTTGCATCCC	9873
rs533066975	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72861030	AATCCAAATTGAACA[A/G]AAGAAAAGAAATAAT	9873
rs533079572	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72948687	TTTTTTTTTTTTGAG[A/C]GGCAGTCTCGCTCTG	9873
rs533087423	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841395	TTTTGCCCTTCAGGC[A/G]AATATGTAGGTTTCT	9873
rs533103598	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72856443	ACAATTCTATAGCAC[C/T]GTATACATGTATCAA	9873
rs533104700	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72850026	ATGACTATCTTTCGC[A/G]CTTACATTTTTCATG	9873
rs533109433	snp	A/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73097384	TTATTTTATTTATTT[A/T]TTTTTTTTTTTTGCA	9873
rs533112709	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73011218	TCTCAACAATATGTG[C/T]AGGTGCCAGCCATGG	9873
rs533115476	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72964882	GCAAGTTCTGCCTCC[C/T]GGGTTCACGCCATTC	9873
rs533122051	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910142	GGAGCACCTCTGCCC[A/G]GCTGCCCCATCTGGG	9873
rs533136889	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73095648	TCCAAAACTCAAAGC[A/G]GGAGTACCTTTGTAC	9873
rs533147842	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842133	TTTAAAGGCTGTTTC[C/T]CTGTGATGAACTAAG	9873
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	9873
rs533160856	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73049581	GGAGATATACCTAAT[A/G]CTAGATGACACGTTA	9873
rs533162646	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115658	ATTTATTTTAAGAAA[C/T]TGGTTCATGCAATTG	9873
rs533170314	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72849235	TCCAACATTCATGTA[A/G]TCATCCCACAATTAT	9873
rs533171004	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72904341	TTGTCCTCAAAACTA[C/T]TAACCTTTTTGTTTT	9873
rs533175797	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72988659	GATATTCAGACACCA[C/T]AGCAGTGACTTCAGG	9873
rs533176736	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72997306	AACTCTAGGAGTAAG[C/T]GAAACAGAATAGCCC	9873
rs533184686	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73089714	TAGAATTTCATTTAT[A/T]CAAAGTGTCTAGAAT	9873
rs533185742	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72970955	GAAGGTCTGAGTCAA[C/T]AGGCAGCATTAATGA	9873
rs533185785	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73012065	CAGTGTACAAAAATA[C/T]ACTTATGTTCATACA	9873
rs533215358	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942252	CCATCTCTCACCATA[C/T]GACATGCAGGCTTCC	9873
rs533225974	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122748	GAAAAAAAGTCTCTA[C/T]TGGACTCTGTGAAAT	9873
rs533230588	snp	G/T	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72889464	ACTGCTGAGTGTTGA[G/T]AAAGTACAGAAAAAA	9873
rs533233667	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73003367	TTTTAAATGAATACA[C/T]AGTAACAGCAGCAGA	9873
rs533253568	in-del	-/A	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73042237	GCTGAGATTATTTTT[-/A]AACTCTGGTGAAAGA	9873
rs533255933	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73130517	TAAACTATCTTCACC[C/T]GCCTTGGGCTGCAAT	9873
rs533259600	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905251	CCTGTGCCTGTGTCC[C/T]GCTCTCCTTTTTTTC	9873
rs533264556	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896586	AAGAAGGCCGTTGAT[A/G]AGATCCTCTTTGTGG	9873
rs533296766	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981191	CTCATTTTTAAGGGG[A/C]AGGAGGGACCAACCC	9873
rs533298815	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72874052	ACCCTGAACTGCATA[C/T]GATCTGGTGCTGCCC	9873
rs533301644	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897092	CAGCTCTCAGCCTCC[C/T]AAAGTGCTGGGATTA	9873
rs533312460	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72882069	AGAATGGCATGAAGC[C/T]GGGAGGAGGAGCTTG	9873
rs533314341	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73065453	AACCGGCACAAGACA[A/C]GGATGCCCTCTCTCA	9873
rs533315283	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941718	ACAAGGGTGCAAGGA[C/T]AGGCACTTTCATACA	9873
rs533329136	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73139340	TTGCTTCACCATGCA[A/G]ATCATCTTCCATTCT	9873
rs533349413	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130037	AGGCACCCGCCACCA[C/T]GCCCAGCTAATTTTT	9873
rs533351942	snp	A/G	0.0130921	0.0798413	intron-variant	FCHSD2	GRCh38.p7	11:73041988	TTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT	9873
rs533367930	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083293	CAGTGGCTCATGCCT[A/G]TAATCCCAACACTTT	9873
rs533389359	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897888	CATTTCAGCAAAAAA[A/G]ATGTATTTTACTTTT	9873
rs533398139	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72850479	CCTCCTCAGCCTCCC[G/T]AGTAGCTGGGACTAC	9873
rs533416955	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137498	GTATACAGTATCTCA[C/T]CCAAGAAAAAATAAG	9873
rs533424594	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72866471	GACAGCGTTTCACCA[C/T]GTTGGCCAGGCTGGT	9873
rs533425274	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881565	GGAAAGGAAATCAGT[C/G]TATCAAAGTCATACC	9873
rs533432399	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114751	AGGGCCTGATGACTC[C/T]GCCCAGTGCCCTATC	9873
rs533442972	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72966969	TTTGGGAGGCTGAGG[C/T]GGGCGGATCACGAGG	9873
rs533448684	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021722	AATAAAACTTAAAAA[A/G]AAAGCTCATTCATGA	9873
rs533474976	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73035256	GGAGCGCAGTGGCGC[C/G]ATCTTGGCTCACTTG	9873
rs533505105	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73082602	CTGACAAAGCCTAAA[A/T]GAGTCATGCCCCAAT	9873
rs533510785	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092496	GTCTATGAATTGACT[A/G]TGGAGCTCCTTGAGA	9873
rs533542578	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73028294	ACATCTTGCAACAGC[A/G]TGCCCTGGATGTGAG	9873
rs533570910	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72918398	TTACCGAATTGCCCT[C/G]TCTAGGACTTCCAGT	9873
rs533571332	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084684	CTGGCATGGGCCAAC[C/G]TGCTTAGCCAGTACA	9873
rs533582961	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72953040	CTGAAAGTGCAAAGA[A/G]TAAGAGATATTTATG	9873
rs533609416	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73020922	CTCTGTCACCCAGGC[G/T]GGAAGGCAGTGGCAT	9873
rs533610344	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928039	CATAGTGAAGATAAA[A/G]GATAAAGGTAAAGGA	9873
rs533610814	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73042415	CCATCCCATTGTTCT[A/G]TGTGTCTGTATTTAT	9873
rs533613078	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974956	AAGAGCTAGAGACGA[C/T]AGAGAAACCAGAAGA	9873
rs533619595	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73006004	CCTCGAACCCCTGGA[A/C]TCAAGTGGTCCTCCC	9873
rs533635586	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73065793	TAGGAATCCAACTTA[C/T]AAGGGATGTGAAGGA	9873
rs533635857	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73062837	TGAAAGGGACAAGGA[C/G]AATGGAACCCAGTTG	9873
rs533645490	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965084	ATGAGCCACCGCGCC[C/T]GGCCAATCATTTTAC	9873
rs533646222	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72868888	CTTAGCTTTTACTTT[G/T]TAAGTTACCTTTTTT	9873
rs533647628	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875399	ACAGAGTCTCGCTCT[A/G]CTGCCCAGGCTAGAG	9873
rs533671263	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921208	ATTTGCCAACCACAG[A/G]AACAATTTATCTTCC	9873
rs533674142	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72925265	TAATCAGGATCATTT[A/C]TGATTATAGATATTT	9873
rs533679357	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72956784	GGAAACTTCAGACCA[C/T]AGCACTATTGCATAG	9873
rs533679504	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73039286	ACTTTGGGAAGCAGA[C/G]GTGGGCGGATCACTT	9873
rs533693584	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066410	CTAGAAGAAAACCTA[A/G]GCAATACCATTCAGG	9873
rs533698299	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966906	GAACCCTGATTATGA[C/G]TTAAGAAAGTGGCCG	9873
rs533699668	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72866348	GATTTTGGCTCCCTG[A/C]AACCTCTGCCTCCCG	9873
rs533708487	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905860	ACATTTGGGTTGGCT[C/T]CAAGTCTTTGCTATT	9873
rs533715107	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860699	AATATACAAAATTTA[C/G]CTGGGCGTGGTGGTG	9873
rs533718393	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113847	TGAAAACTTGTAGTG[G/T]TACTGCCTTAGTGGT	9873
rs533720545	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858166	ATACAGAGGAAGACA[A/G]CTCCTCAATATTTAC	9873
rs533744758	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73037347	ACAGTCTATGTGTCT[A/G]GACAAACATATAGTG	9873
rs533746944	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108452	GGTTGCCTGTGCTTG[C/T]GTAGTATTACTCAAG	9873
rs533767455	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73015938	ATGCCATAAAGGAAG[A/C]TCTTTTCCTTAAAAT	9873
rs533774418	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72968891	AAGATATTTCTATAA[A/G]TTGGTAAACAAAACA	9873
rs533786150	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73009243	GCTCACGCCTGTAAT[A/C]CCAGCAGTTTGGGAG	9873
rs533810677	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061251	GGAAGCCATGAGGGA[C/T]TGAGCCTGAAGAACT	9873
rs533825702	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144343	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	9873
rs533826868	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008202	AAATTAGCAGGGCAT[A/G]GTGATGCACACCTGT	9873
rs533832822	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73118911	CCTCTCTTAGACACA[C/T]ACTACACAACATGTA	9873
rs533846255	snp	G/T	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:73108559	GATTTAAGTTTTTTT[G/T]TTTGTTTGTTTTTTG	9873
rs533847674	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73075726	AGACTGACGCATGAG[A/T]ATTTCTTGAACCCAG	9873
rs533869258	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73114589	CCAAGACCCACAGCG[C/T]ACTAACTAGGTATTG	9873
rs533889960	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73008919	AATATATTATTATTA[C/T]CAGTTCATAGTCAAG	9873
rs533896582	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999699	AAGAGAAAAGCACCA[G/T]AGGTAGTTAAACTCT	9873
rs533902588	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72892077	GAATGAATTTGTAGG[A/G]AGTAGCTAGATGAGA	9873
rs533906106	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901130	GACATCGTGGCTCAC[A/G]TCCGTAATGCCAGCA	9873
rs533913568	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067588	CCCCAATATCATCAT[A/G]TTCAAGATCCCTGAA	9873
rs533913668	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076671	ACATACTTAAGATTG[A/G]TGAATCATTAATGGT	9873
rs533930190	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73045024	GCAGTGAGCCGAGAT[C/T]GCTCCACTGCACTCC	9873
rs533930803	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72922071	TTAATAATAAATGGA[C/T]AAAAGATACAGATTG	9873
rs533935060	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72944978	TGGCCATACTGCCCA[A/G]GGTAAATTATAGATT	9873
rs533936062	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72976126	GCAATAGTTTTTTGT[C/T]TGTTTGTTTTAGTTT	9873
rs533937035	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73136784	CCTGTAATCCTAGCA[A/C/T]TTTGGGAGGCCGAGG	9873
rs533939719	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72901865	ATTAATTCTATTCTG[G/T]TTTTTTTTTTGTTTG	9873
rs533952669	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023709	TTCACAAAAAAACCT[A/G]AGCACAAATGCTTCT	9873
rs533976227	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967655	GGGTATAGAGCTTTT[C/T]TGGGGGATAACAGAA	9873
rs533990020	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045323	ACACTGTTGGTGGGA[A/C]TGTAAACTAGTTCAA	9873
rs533992897	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72937419	GCAAGAAATATAAAG[A/C]CTTAGTGTTAATTCA	9873
rs534013800	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72965118	TTAATTCAAAGGTCT[C/T]TGATAGATCCCCATT	9873
rs534034368	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885314	ACGGATCTGCTACAA[A/T]GGTTTTAGCATACTA	9873
rs534042465	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143243	GAGGGAAGCCTTTCT[A/G]AAGGTTACACAGCAG	9873
rs534052492	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73039100	TATTTTTATCTGCAA[C/T]CAGTTTCAAACTGGA	9873
rs534073045	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72861626	CTAGCAAACCAGTTC[C/T]AATCAATATATAGAA	9873
rs534084759	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72931125	TTTTGAAAAGGAGTC[A/G]CGCTGTGTCACCTAG	9873
rs534112908	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039790	TTTGATGACTTTAAG[C/T]GTTTAATTATTCCAC	9873
rs534115663	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73032015	AAATTATGGTCATCA[A/G]TATGCTGCAATGTTA	9873
rs534118928	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73070919	GAATTTAGTTTGATT[C/T]AGAAGTAAAACCTAG	9873
rs534119326	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72907442	TGCTTCCAGTTTTTG[C/T]CCATTCAGTATAATA	9873
rs534120556	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061638	GTGGGGAGAGACGTC[C/T]GCCATTGCTGAGGCT	9873
rs534138795	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853488	GGCGCAATCTTGACT[C/T]ACTGCAACCTCCGCC	9873
rs534146231	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100943	ACCCTTTTCTCAGAG[A/C]TCTCCTCACACAGAC	9873
rs534167204	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931948	TTATCAGACTGACTT[A/G]TATTTTGACCAGACA	9873
rs534172212	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73128206	GAATACAAATAATTT[A/C]TATGGAGTCTCTAAT	9873
rs534175803	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024730	TGGGAGAAAATACTG[C/T]AAACTACGCATCCCA	9873
rs534176646	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73068135	TCGCACAACACATGG[G/T]AATTATGGGAACTAC	9873
rs534180467	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952866	AGATATATAATAAAG[A/C]AATAAAAGCCTACTC	9873
rs534183315	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72879639	TTCACAAGATGGCCT[A/T]AACAGTAGTTTATAC	9873
rs534183485	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72968673	ATGGAATTTCAGAAG[C/T]CCTGCAAACTTTCTC	9873
rs534187544	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72879008	CCAGCTACTTGGGAA[A/G]CTGAGGCAGGGGAAC	9873
rs534187953	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73053977	GTATTTTACAAAAAT[A/G]TCCATCTACAAATTT	9873
rs534201542	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72992110	ACAAGCATTCTTATA[A/C]ACCAATAACAGACAA	9873
rs534202395	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72924167	GCTGGACTCAAACTT[C/T]TGGGTTCCAGTAATC	9873
rs534207807	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915295	ACTTTTACACTGTTG[G/T]TAGGAGTGTAAATTA	9873
rs534213450	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101901	GAATATATTGTGTCT[A/C]TGTATGAAAACAGAT	9873
rs534227638	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72862503	TAGCACCAAAATTAT[A/G]AAATAGGGGTAAGTC	9873
rs534232169	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945643	GAATATTTTTGCAAT[C/T]TACTCATCTGACAAA	9873
rs534264524	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73070395	ACGCCAGTCGTAAAG[A/T]AGATACTTGATAAAT	9873
rs534273525	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73012435	TGGAAGATGCTTGGG[A/C]AATGATATTCTTTAT	9873
rs534275616	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73094103	GTAATCCCAGCTACC[C/T]GGGAGGCTGAGGCAA	9873
rs534279141	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72993484	TTGTGGCACTATTCA[A/C]AATAGGAAAGACTTG	9873
rs534283861	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73079842	TCTATAAATGGGCTC[A/G]ATTTTCCCAAGCAGA	9873
rs534321714	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057739	CTATTAATCAAGCTC[A/C]GTCCCTAACCCTTTA	9873
rs534329053	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905412	AAGCATTTATCCTTA[C/T]TTTGTATTACAAAAA	9873
rs534336500	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72885929	TGGAGGTGGGGTTAC[C/T]GGGGTTTCTCCAGCC	9873
rs534341308	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73094885	TTTAACGAGGCAAGC[A/G]GAACGAACAACTGAA	9873
rs534349038	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72999031	CAGAAAAGCAGAGCT[A/C]ATGGATGGAAAGAAA	9873
rs534350789	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850847	GTAATCCAAGCACTT[C/T]GGGAGGCCAAGGTAG	9873
rs534370356	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72851780	CAAAACAAGAAAAAA[A/G]ATAAAGTTCGTGAAG	9873
rs534374468	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142342	CGCCCCCGCCCGCCC[A/G]GGAGGAGGAAGGTGG	9873
rs534386716	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72948901	GGATCTCCTGACCTC[A/G]TGATCTGCCCACCTC	9873
rs534414596	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897269	ATATCTGTGGGTTCT[A/G]TATCTGTGGATTCAA	9873
rs534415870	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72986354	AGCTGGGACTACAGG[C/T]GCCTGCCACCACGCC	9873
rs534416537	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72884429	AGTGAAACCTCACAG[C/T]AACAGGCCCAGAGGT	9873
rs534417652	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73087235	AAAAAAATAAAAATT[A/T]GTAAAAATAGTCAAA	9873
rs534424408	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72941863	ATCTTAAGGAAGTTA[A/T]CAAAGAGGTGTATTA	9873
rs534424731	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042171	ACTTCAGGTGATCCA[C/T]CCACCTCAGCCTCCC	9873
rs534428882	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72845173	CGTCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA	9873
rs534451930	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978012	TCATGTCCTTTGTAG[G/T]GACATGGATGAAGCT	9873
rs534479343	in-del	-/ACACACAC	0.301932	0.244547	intron-variant	FCHSD2	GRCh38.p7	11:73051869	TAACACGGTATATAA[-/ACACACAC]ACACACACACACACA	9873
rs534486427	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870387	TATGTGTTCAGTAAC[C/G]TTTTTTGAATAAATA	9873
rs534487215	snp	A/C/T	0.00239393	0.0345281	intron-variant	FCHSD2	GRCh38.p7	11:73078932	ATTATGTTGTCAGGC[A/C/T]GGTCTGAAACTCCTG	9873
rs534487895	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042624	TTGATAGAGACTGCA[C/T]TGAATCTGTTGATTG	9873
rs534502446	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934249	TTTAAATGAGCAAAA[C/T]ACAAGAATGTTCTTT	9873
rs534513157	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73044971	GTTACTCAGCAGGCT[A/G]AGGCAAGAGAATCAC	9873
rs534518504	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025457	GAACACATGCACACA[A/T]AGAGGGGAACAACAG	9873
rs534521263	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72995798	ATAACTTGAATATAA[G/T]AATACAAATAAAAGT	9873
rs534525978	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081990	GGCGGATCACCTAAG[A/G]TCAGCAGTTCGAGAC	9873
rs534533658	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73090926	AATCACGCTTCATTC[C/T]CCTTTCTTCTCCTCC	9873
rs534546160	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72871087	GGAATAACTGCTTAT[C/T]CTTTAGCCCTTGTTC	9873
rs534553396	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035388	TGCCCGGCTGTTCTC[A/G]AACTCCTAAGCTCAA	9873
rs534554069	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969331	GCTTTAAGTTATTTA[C/T]ATCAGGAATAAAAAT	9873
rs534557131	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72849594	GCAAGTGAAAGACGT[C/G]AAGTCAGAGCCTAAA	9873
rs534580226	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73033061	TGGGGGGCTGAGGCA[G/T]GCGGATCATGAGGTC	9873
rs534583845	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73082855	TTATCTTTGTACATG[A/G]AAGAATAGTTATTAA	9873
rs534590867	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72948196	TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGT	9873
rs534593494	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73060152	GAGTTAGTCACCCAA[C/T]AGATTCATTGAATGA	9873
rs534614813	in-del	-/A	0.212122	0.247114	intron-variant	FCHSD2	GRCh38.p7	11:73087705	GCGAGGCTTTGTCTC[-/A]AAAAAAAAAAAAAAA	9873
rs534616987	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995559	AAGTACAAAAATCAG[C/G]CAGGTGTGGTGGCAA	9873
rs534618293	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896759	AGCAATTAGGGGGAA[A/G]ATACTAAAAAAAAAA	9873
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	9873
rs534623152	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72850187	CGTGCCTCAGTCTCC[C/T]GAATAGCTGGGATTA	9873
rs534657681	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72972487	TAGGGAGTGGGGAAA[A/C]CACACAAAGAGGAAA	9873
rs534661050	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73093787	TTTTTGTATTTTTAG[C/T]AGAGACAGGGTTCTT	9873
rs534669883	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72918736	AACATTGTTATTTTC[C/T]GAATTCTTTTTTTAA	9873
rs534683844	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965183	CCATTCATATAACTT[C/T]CTAGAATCCAGCCTC	9873
rs534717818	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73024866	AAAAACAGACATACA[C/T]GCAGCCAACAATCAA	9873
rs534725172	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73090683	AAACTGGCAGTATTA[A/G]TAGAAGAAAGACCTT	9873
rs534730845	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73140007	GACAAACAGAAGTCC[G/T]TGAACTATTTACTAT	9873
rs534742598	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842525	CCGGTGAGGGTAAGG[A/C]AGAGACTGCAGCCCA	9873
rs534744630	snp	G/T	2.41882e-05	0.00347757	intron-variant	FCHSD2	GRCh38.p7	11:72988937	TTATTTGCATAATAA[G/T]TTTCTCAGAAATGTT	9873
rs534758975	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066654	TACAAGAAAAAAAAA[A/C]CCATCAAAAAGTAGG	9873
rs534765147	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72957039	TTTTTTTTTCTTCTT[C/T]TTTTTTATTATACTT	9873
rs534770188	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115848	TTGAGGGTAGCCTCC[C/T]TTACTTAAAGTCAAC	9873
rs534781809	in-del	-/G	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72889462	ACACTGCTGAGTGTT[-/G]AGAAAGTACAGAAAA	9873
rs534802178	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72958006	TGATAAATGTATACA[A/G]TATCTGAATCTACAG	9873
rs534817448	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123094	AATTAACATGAACTA[C/T]ATATACATTAAAGAA	9873
rs534834300	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059422	AAAACATTGTGTCAG[A/G]TAAGTGTTAGCCATC	9873
rs534844100	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851685	GAGGCAGAGGTTGCA[C/G]TGAGCCGAGATTGTG	9873
rs534844135	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72843746	AAAAACTCAAGAAAC[C/T]GAATCCTCAAGAGGC	9873
rs534850132	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73038083	TATTAAAAACAAAAC[C/T]ATCTATCACTAAAAA	9873
rs534850451	in-del	-/GTAC			intron-variant	FCHSD2	GRCh38.p7	11:73035206	TATGTATGTATGTAC[-/GTAC]TAAGACAAGGTCTCG	9873
rs534857599	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028094	GGAGCCCCCACACAG[A/G]ATGCTCACAGGGGCA	9873
rs534871459	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882214	TTGGGAGGCCAAGGC[A/G]GGTGGATCATGAGGT	9873
rs534872513	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73020315	TAGAAGGGTGCTCTA[C/T]GGCTCTAGCACAGGT	9873
rs534874131	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122185	TAAAAGGCAAAAAAA[A/G]AAAATGTAGCTCAAA	9873
rs534880533	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971865	AGTTTGTGGTGATTT[G/T]TTACATAGCAACGGA	9873
rs534885275	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72992811	ATAAAAACCCTAGAA[G/T]AAAAGCTAGGCAATA	9873
rs534914343	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73099170	CAGTAAGCTATGACT[A/G]TGCCACTGCACTCCA	9873
rs534922304	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72866026	CCTGCTCAGTTCAAA[C/G]TCAGATGGTATATGG	9873
rs534933902	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130109	TCAATCTCCTGATCT[C/T]GTGATCCGCCCGCCT	9873
rs534936697	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72917881	TGACAGAGTGAGACC[C/T]TGTCTCAAATTAAAA	9873
rs534946475	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73062861	CCAGTTGGAAAACAC[A/T]CTTCAGCGTATTATC	9873
rs534982356	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990703	CTCTGGGACACATTC[A/G]AAGCAGTGTGTACAG	9873
rs534983873	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73021316	TCGACCTAAATGGCC[A/G]TCAATGGTAAAGTGG	9873
rs534984287	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73097550	ATTGGTGTTAATTCA[A/T]CATTAACTGTTTGGT	9873
rs534985286	in-del	-/TAT	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73030873	AAATCCTGAATACAA[-/TAT]TATTAACTATAGTCC	9873
rs535008647	snp	A/G			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141445	ACGGGCGGGGCTGGC[A/G]ACAAGCGGCTGGAGG	9873
rs535016278	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116647	CTGGGCACAAGCTCC[C/T]GCGTCAGCCTCCCAA	9873
rs535017455	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137758	ACACAGGGGCATGAA[C/T]GTAGAGTGCACAGTT	9873
rs535020118	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73093659	CAGGCTGGAGTGCAA[C/T]GACGCGGTCTTGGCT	9873
rs535024364	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72991134	TGATAAATTCCTCGA[A/C]ACATACACCCTCCCA	9873
rs535045704	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848682	CATAGTCTATTTAAC[A/G]CAGGGATGTGCCTGG	9873
rs535049150	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72996432	ATAAATGTGAAAGAT[-/A]ACGGACAAAAGTATG	9873
rs535049164	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73013456	CAAAGGACAGACAAC[A/G]TATCTTCTAGCCTCT	9873
rs535061023	in-del	-/AG	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73069933	AATATGTAAAAAAAC[-/AG]AGTCACAGAAAATTA	9873
rs535073098	snp	A/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73107051	TATATATATATATAT[A/T]TTTTTAAATGGAGTC	9873
rs535080657	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73058721	CTGCCTCAGCCTCCC[A/G]AGTACCTGGCTAATT	9873
rs535100226	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913097	AACAACCAGATCTCA[G/T]GAGGACTCACTCACT	9873
rs535114734	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72978382	GAATAGACATTTCTC[-/A]AAAAAAAGTCATATA	9873
rs535128494	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969320	AATTTAATTTGGCTT[C/T]AAGTTATTTATATCA	9873
rs535130383	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960740	TTGGGAGTTGATGTG[G/T]AGAAAGGGTATGGGG	9873
rs535137763	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72983581	AAAAATATATTTTTA[A/G]TAGAAATATTCTTTT	9873
rs535148509	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72844281	CAAAGAACTATGTAC[A/G]TGAATTTGATGATAG	9873
rs535151290	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73052282	AAATTTTGTGTAACG[G/T]TATATTCTGATGGTG	9873
rs535175487	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73061726	GGTGGAGCCCACTGC[A/C]GCTCAGCAAGGCTGC	9873
rs535181135	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72881885	GGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG	9873
rs535190236	in-del	-/AG			intron-variant	FCHSD2	GRCh38.p7	11:72853438	GATTTTTTTGGAGAC[-/AG]AGTCTCGCTCTGTTG	9873
rs535198563	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72906869	GCACGATGTCTCCAG[C/T]TTTGTTCTTTTTGCT	9873
rs535216386	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73126040	ATATGTTTGCTTGTT[G/T]CAAGACAAAAGAATT	9873
rs535219087	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051473	TTACACCTAATTTAC[A/G]AACAGAAAAAGTTTA	9873
rs535232139	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855119	TCTCTACTAAAAATA[C/T]AAAATTAGCCGGGTG	9873
rs535238260	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953197	AGGAACATTCTTTGA[G/T]AAATGGTCTTGAGAA	9873
rs535239364	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109929	AATTTTATTAAATGC[C/T]TTTTGAGCATCAATT	9873
rs535255634	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72955367	AAGGTATGGAAGAAG[A/G]CATGTGAGGCTTCCA	9873
rs535268681	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902172	GAGCCACAGCGCACG[A/G]CCTACTCTGGTTAAA	9873
rs535287057	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847838	GCTGAGATTACAGGC[A/G]CCCGCCACCACGCCC	9873
rs535287684	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052122	AATGCAAAGATAGTA[C/T]GGCATTTCCTTTGGT	9873
rs535297459	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110453	ATTATGCATTCCTTC[C/T]AGATTTTTCAATTTA	9873
rs535298276	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043424	TTTCTATTTGCTTAA[G/T]TGTTCTTTTCCATTT	9873
rs535300892	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72960414	TGCTCTAGTCTGCTG[C/T]TCCTTTGGATTTAAA	9873
rs535321413	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72952743	AAAGATAAATGAATA[C/T]TTACAGAACACCTAC	9873
rs535331284	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943937	AATCATTATTCATTG[G/T]GATGCTGCCAACTTT	9873
rs535352958	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044290	ATGAATATTTCCAAA[G/T]TCAGAGGCTGAGTGT	9873
rs535360805	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891211	TGTTCAAATTAGAGG[C/G]ATGAGCCAGTACACC	9873
rs535363287	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002298	CCAGATGAATCGGTT[C/T]AGATGGAAATAGTCA	9873
rs535380527	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73018151	CATCTGTGGTCTGTC[A/G]GAGCCCCTCCAAGTT	9873
rs535390549	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946934	ACAAGGCAGCACCAG[A/G]TGCCCCTCTTTGTGG	9873
rs535393290	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72886650	GAGTAGATAAAAGTG[C/T]GTGCACAGGTCCTCC	9873
rs535395266	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986493	GGATTACAGGCGTGA[A/G]CCACCGTGCCCGGCC	9873
rs535397222	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72994642	GTGGTGGTGGGCGCC[C/T]GTAGTCCCAGCTACT	9873
rs535427955	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72941753	TTTCAGAAGTATATA[C/T]TGATATAATCTTTTC	9873
rs535431281	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73066664	AAAAAACCATCAAAA[A/G]GTAGGCAAAGGATAT	9873
rs535448576	in-del	-/AA	0.0202498	0.0985639	intron-variant	FCHSD2	GRCh38.p7	11:73049874	CACAAAAGGACCATA[-/AA]AAAAAAATTGTTTTC	9873
rs535472673	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025265	AGTGATAGACTGGAT[A/T]AAGAAAATGTGGTAT	9873
rs535475838	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879209	CGGCATTAGTATAGG[G/T]CTAATTTCTAATTTA	9873
rs535481608	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72991545	ATCCCCGGGATGCAA[C/G]GCTGGTTCAACATAC	9873
rs535490507	snp	G/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839719	ACTCATTTTTGCTGA[G/T]TTTTGGGGATCTGGG	9873
rs535501981	snp	A/G	1.67346e-05	0.00289258	intron-variant	FCHSD2	GRCh38.p7	11:72887621	TGTTTTTTACTTTTC[A/G]TCTTCCTTAAGTGAT	9873
rs535509399	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73070314	ACTCTGTTTTACTGA[A/T]AACATTCCAGCACTA	9873
rs535515722	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862327	TATTTGCAGGTGACA[C/T]GGTTATATAGAAAAT	9873
rs535520766	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73029103	ACCATAAATATAATG[A/G]TGTAGTACACTAAAA	9873
rs535530613	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909137	CCTGCCTTGGGCTCC[C/T]GTGATTCTCCTGCCT	9873
rs535536608	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121860	GATTAGGGATAAGCC[C/T]ACAAAACTGCATTTT	9873
rs535550142	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138494	GCCTTCCTGAACTGC[C/T]TCTGAAAATGTATTA	9873
rs535554819	snp	G/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73026545	AATATATAAAACAGA[G/T]ATACAGTGCTCTAAA	9873
rs535571105	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72971065	GTTATCCCTACTGAC[C/T]CCCCTGCCCAAAGTA	9873
rs535571815	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062371	TTCCAAAAGCCAAAA[C/T]GCCTCTTCTCCTCCA	9873
rs535579271	snp	C/T			synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843266	GCTCAGGAGGCTGTT[C/T]GAGGTGGGAAACTGT	9873
rs535579437	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73025703	ATCTCCTTGGAATTA[A/G]TTTGTAGAATTATAA	9873
rs535585082	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73031709	CAAGCCTTCTGACTC[C/G]AAGGCCAGTCCACAC	9873
rs535590195	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009937	TCCAGTATCTGGATG[A/T]CTAAATCTCGTTAGA	9873
rs535601571	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72979961	ATGTCCAGGAAATAC[A/G]AAAAGAACATAAAAT	9873
rs535609622	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73092651	TTTTCAGACTCTTCA[C/T]AAATTTGATTAATAG	9873
rs535621824	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027333	CTTTAACAGAGAGAC[G/T]GGCAGCATTTTGCCC	9873
rs535634212	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72873277	GAGGCTGCAGTGAAC[A/C]GAGATCGCGCCACTG	9873
rs535634634	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925655	GAGATAATAACTGAC[A/G]CACGTATCCCAGGGT	9873
rs535638082	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137610	CTTCATCTGAGGGAG[A/G]ATGCCAGAACCATGT	9873
rs535643735	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054975	TGAGACTGGGTAGTT[C/T]ATAAAAAGAGGTTTA	9873
rs535657685	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902926	CAAGAAGATAGTTTT[A/T]ACACAAAAAGCTATT	9873
rs535678446	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019319	AGGCTTTGTTATCAC[C/T]ACAGAGAAATTGGAC	9873
rs535696086	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909913	AGGAGCACCTCTGCC[C/T]GGCTGCCCATCATCT	9873
rs535699650	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046322	GAAAAGCCTTATGAA[A/C]TGATTTTAAAAAGAA	9873
rs535707780	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055542	ATGATAGCAGAAAGT[A/C]ATCAAAAGATACTGA	9873
rs535709425	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946235	AAAATGATGAGTTCA[C/T]GTCCTTTGTAAGGAC	9873
rs535724003	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72916932	TTTTGAGTTAATTTT[G/T]TGAGGTAAGGGTTCA	9873
rs535733540	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910344	AGAGACAGCGACCAT[C/T]GAGAACGGGCCATGA	9873
rs535753859	in-del	-/T	0.499968	0.00399348	intron-variant	FCHSD2	GRCh38.p7	11:73138605	TATCTTGCACAGGAA[-/T]TTTTTTTTTTTTTTT	9873
rs535756388	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144311	ACAAGGTCAAGAGAT[C/G/T]GAGGCCATCCTGGCT	9873
rs535767304	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72996550	ATTTTGAAAAATGTA[A/G]TAATTCTCATAATCC	9873
rs535774961	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73139453	CATCCCTCTAGTAAG[A/G]AAGATACTGATTTTC	9873
rs535775957	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73035845	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGACTA	9873
rs535777373	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840100	TCCAGCCTCCTAATC[A/G]CTCCCTATATCCTTT	9873
rs535779758	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115785	CTTCCAGATACCTCA[A/G]TTTTGTTCCTAAGGC	9873
rs535795725	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096229	ATTTAAAATGAATTT[G/T]TAAACTTCTTGTATT	9873
rs535814433	in-del	-/ATAA	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72975628	TATCACACATACACT[-/ATAA]ATATATAGTTATTAT	9873
rs535816248	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956376	TATGCTAAGGCTGGT[C/G]AGTGGAGGTCTGACA	9873
rs535818127	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856788	AGAATCACAGACTTA[C/T]GATTCTATTGTTTTC	9873
rs535818573	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040793	TGATTACACTAATCC[A/G]ACTGTGCTATAAAAT	9873
rs535830314	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73044692	TTAAAATTAGGCAAA[C/T]GCTGGGTAAATACTA	9873
rs535837470	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73122868	TTTACAAAGAATCTA[C/G]AAGATATGCAGATTA	9873
rs535852400	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043346	TTATCAGTTTCCATA[A/C]GCAAGTATTTATCAT	9873
rs535858494	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088078	ATTCCTTGCTATGTT[C/T]CCTAGGCTGGTCCTG	9873
rs535863561	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882398	TGATGGTTATCAGAA[A/G]CTGGGAAGGATTATG	9873
rs535868114	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73119401	AAATCTATATACTTT[A/G]AAATTTTTATGTGCT	9873
rs535872334	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72990543	AACTAGAACTCAGGA[C/T]TAAGAAACTCACTCA	9873
rs535875216	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72977081	AGGTGCCCACCACCA[C/T]ACCTGGCTAATTTTT	9873
rs535880493	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72932868	ACAAATAATAACACC[A/T]ATCAGAATTCGCATG	9873
rs535881950	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033403	AGATGTAAATGGGAC[A/T]AGTTTTAGTGCAAAG	9873
rs535904708	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72979003	GCTGGGACTACAAGT[A/G]CATGCCTCCACACAC	9873
rs535912198	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036383	ATTTCACAACGTTAT[A/G]TCGGTCTTTGGAGTC	9873
rs535918457	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72946982	ATCTATGCAATAGCT[C/T]ACCCAGCTACCCAAG	9873
rs535918546	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72908857	TGGGGTTTCACCATG[A/T]TGCCCAGGCTGGTCT	9873
rs535931002	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73080153	AATAAAAATACTAGA[C/T]GGGTATGGTGGCATG	9873
rs535967235	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72924876	TTAAGTCTGAATAAA[C/T]TTCCTGTATCAGGAC	9873
rs535979353	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72943559	GAAGGAAATTGAAGA[G/T]AATGACAGGTGAGAC	9873
rs535987753	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928524	CTTAAATGATAATGA[C/T]GGTTAACACAGGCAA	9873
rs535992534	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970338	GAGTAAAAATACTTA[A/C]AATTCTAATGTATGA	9873
rs535998585	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72851250	CTAAACATACCATTG[A/G]TCTAGCAATTCCGCT	9873
rs536002745	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916381	GTAGTAGCATGATCA[G/T]AGCCTGCTGCAGCTT	9873
rs536004401	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876028	AAACCAGCAAAAGAA[A/G]TGACTAGTTGGCTTG	9873
rs536006242	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72983077	AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA	9873
rs536016137	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025930	TACTGATATGCTCCA[C/T]GTTTTGACTAAAAAA	9873
rs536028861	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73056618	CATTCATTCATTCAT[C/T]AAATAAACATTCACC	9873
rs536070044	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72921067	GCCAGTTCTCACTCT[A/C]CCTGACAAAAAAAAA	9873
rs536071071	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73023083	CCTCAATATAAAGCA[C/T]AAAACTATGAAACAT	9873
rs536083947	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72846460	GCTGGGATTACAGGC[A/G]TGAGCTACCGTGCCC	9873
rs536091438	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73133703	CAGGAGGCTGAGGCA[A/G]AATTGCATGAACCCA	9873
rs536091703	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141736	CGGCAAGTCGGTGAC[A/T]AGCCCAAGACGAGGG	9873
rs536108895	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72963581	AGCCCCCAACCTTTT[C/T]GGCACCAGGGACCAG	9873
rs536110246	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73090248	TTTTTTTTTTTGAGA[C/G]GGAGTCTCGCTCTGT	9873
rs536126017	snp	A/C	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72913822	AAAAACCAAAAAAAA[A/C]CCAAAAAAAAAACAA	9873
rs536130827	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067444	GTAACAAAACTGCGC[A/G]TTCTGCACATGTATC	9873
rs536134703	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011421	TGCCCCAGCACCACT[C/T]GCTCCCCAGCAGCAC	9873
rs536143368	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72881126	CTTGCAAATTATTCA[A/T]GCAACAAGGGACTAA	9873
rs536152620	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73141169	AGCCGGGTGCATCCG[C/T]CACTCCCACCCTGGT	9873
rs536165787	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73124489	GGCCAGGCGCAGTGG[C/T]TCACACCTGTAATCC	9873
rs536183104	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73056940	ACAAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC	9873
rs536188863	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73060316	ACCTATTTATTATTA[C/T]TATCTGTCACCAGCA	9873
rs536195235	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955229	CACCTTTCTTAGGGT[C/T]GATTAGTTTGCTATA	9873
rs536196576	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72878380	TATCCCTAGCTCTAA[C/T]AACAAAGAAAAGATA	9873
rs536204985	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73006909	TTTGAAACCAAATGT[A/G]TCTGGCTCCCAAACC	9873
rs536218703	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907815	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT	9873
rs536231730	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951496	CTTGGCATTTAGCTC[A/G]ATAAATGTTTGCTCT	9873
rs536242589	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935508	CTTAAAATTAAATCA[C/T]GAAATTCTACAGTCT	9873
rs536243062	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73121411	GGAGGATACCAGAAA[A/C]GGCCTCATAAAGCAT	9873
rs536248653	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908472	AACTGTTTTCCATAG[C/T]GGTTGTACTAATTTA	9873
rs536252962	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836370	CCAGTGGTCACATCC[A/G]GCAAGGGGACTTCAG	9873
rs536259680	snp	A/G	0.00207507	0.0321439	intron-variant	FCHSD2	GRCh38.p7	11:72900317	ATCCACCAGTTGGGC[A/G]GCTTTTAAACTCTGC	9873
rs536269781	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72845225	CAGCAGTTTGAGACC[A/G]GCCTGGGCAACATGG	9873
rs536278733	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936234	AGAGAATTTCATCTA[A/T]CTCCCTTGTAAGCCT	9873
rs536305754	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73052937	CTGCAACCACCGCCT[C/T]CTAGGTTCAGGTGAT	9873
rs536318914	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72903464	GACCTCGTGATCCAC[C/T]GGCCTCGGCCTCCTA	9873
rs536326793	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73092389	CAGTGATTCTTCCAC[C/G]TCAGCCTCCCAAAGT	9873
rs536335769	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73083822	ACACCTTCAAATACT[G/T]CCTGGTTAAGATATG	9873
rs536343102	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891781	TCTGAGTCGTAGCTA[C/T]ATCTGAAAACTAGTG	9873
rs536351777	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037248	TCCCCCACCACAGTG[C/G]TACATTTACAATGGA	9873
rs536366192	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73126147	AAGTTCGAGACCAGG[C/T]TGGCCAACATGGTGA	9873
rs536368812	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72873350	AAAAAAAAATGAATC[C/T]TTTCATGTGCTTATT	9873
rs536378676	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72973988	AGTGCAAATGAAGGA[A/G]CAATTAATTGTGAAA	9873
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	9873
rs536394849	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074947	TGGGGAGGGAGGGAG[A/G]CAGGGAAAGAAAGAC	9873
rs536408751	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72929246	TATACCCAGTAATGG[C/G]ATGGCTAGGTCAAAT	9873
rs536424453	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038412	AGGGACCTTATAATT[C/T]ATCCAGTCGAATCCT	9873
rs536427759	snp	A/G	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:73045245	ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA	9873
rs536440846	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72857637	TTTTTTTAGTAGAGA[C/T]GGGGGTTTCACTATG	9873
rs536446936	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72984329	CAAGAATAAAGGTAA[A/C]CACGTGCGGAAAACA	9873
rs536462267	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075590	GGAGGCCAAGGAGGA[C/T]GGATCACTTGAGGTC	9873
rs536469445	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085639	CAGGTTCACAAAAGA[A/C]TTCAGAAGACCTGAT	9873
rs536473040	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930389	CCAATCTGTCCCAAA[A/G]TGCAATTCTTGTTTT	9873
rs536475536	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938665	GGTTTGTCTGGAGAG[A/G]GTCAATTTTCATCAT	9873
rs536489058	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73031089	TGGATGGGTTCATCC[A/G]GAATATGTTAAGTGA	9873
rs536495707	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921013	TTTGGACACTGTCAT[G/T]TGAAAATGGATATCC	9873
rs536502829	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966641	ACATTCAACAGATAT[A/G]TATGTCAGTTACTGT	9873
rs536503422	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73116829	GGCATGAGCCACAGC[A/G]CCTGGCCCATATCTC	9873
rs536513005	in-del	-/T	0.475702	0.107512	intron-variant	FCHSD2	GRCh38.p7	11:72924441	GCCACCACACCCGGC[-/T]TTTTTTTTTTTTTTG	9873
rs536526506	in-del	-/AGA	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73096156	GAAAAACATGGTAGC[-/AGA]AGGACACCCATGAGC	9873
rs536530708	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72868723	AACAAACAAACAAAC[A/C]AAGAAACTATATAAC	9873
rs536531555	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086235	CCAACATGGCAAAAC[C/T]CCGTCTCTACTAAAA	9873
rs536534070	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72976355	GGAGTGCTGTGGCAG[A/G]ATCATAGCTCACTGT	9873
rs536534966	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72859744	TGGTCAGTACATATA[G/T]GTGAAGAAATTACCC	9873
rs536536678	snp	A/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72844233	TGGAACTGCTACCAG[A/G]GGGCTCCCATGGACA	9873
rs536537665	in-del	-/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73005601	TCTCTTCTCTAACTA[-/C]ATTCACTCTGTTGAA	9873
rs536541581	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72923738	AGAGATCAGGAGTTC[A/G]AGACCAGCCTGGCCA	9873
rs536552479	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73077232	CAAACAACCCAATTT[-/A]AAAAAAAAATCAATA	9873
rs536564510	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124137	AAGCTGGAAACCATC[A/T]CTCTGAGCAAACTAT	9873
rs536566298	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72922386	ATATGTATATTTACT[C/G]AACAGCAGTGACAGA	9873
rs536570292	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73014913	CAGTGACATGATTTC[G/T]GCTCAATGCAACCTC	9873
rs536584411	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067992	TGGTGACAGACACGA[C/G]AGAATAAGAACCAAG	9873
rs536596095	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73077768	AGCTGGGAGAGAGGG[A/T]TTATAAGGACACACA	9873
rs536605873	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852726	ACTATTTATACTAGC[A/G]AAGACATGAAATCAA	9873
rs536621200	snp	A/G	3.40379e-05	0.00412526	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73015822	ACCTGTAATCATTCC[A/G]ATCATCAGCTTTTAC	9873
rs536622414	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963412	CTAAGTGAGGCATAC[A/C]GAAGGGAAATAATTT	9873
rs536629149	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959673	TAAATTGCTAAGATA[G/T]ACATTTCAACGCACC	9873
rs536639343	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083534	AGCCTCGCAACAAAG[C/T]GAGACTCCATCTCAG	9873
rs536644451	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064055	GTAAAACACTCCTCA[C/G]CAAATGCAAAAGAAT	9873
rs536645992	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061174	AGGCGAGCCGAAGCA[C/G]GGTGGGGGGTCACCT	9873
rs536650004	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910281	CTGGGAAGTGAGGAG[C/T]GCCTTTGTCCGGCCG	9873
rs536659622	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72999011	TGTTAGTGAGTGAAG[C/T]CATTCAGAAAAGCAG	9873
rs536682583	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73104013	AAAAATACAAATAAA[C/T]GTTTTCTGTTATTAA	9873
rs536685531	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73007923	ATTTATTATTTCTGA[C/T]GACTATGTGTGGCTA	9873
rs536706211	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056794	AATAAAATCCATAGA[C/T]TGACAAGGCCGGGCG	9873
rs536711612	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955143	CTGCTCCCCACTTCA[A/G]ATGCTAATTGGAAGT	9873
rs536714040	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952112	ACAGGAAGAGCACCC[A/G]TGAGTTTAATGCTTG	9873
rs536741543	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72900977	CGTGCCTTCTCATTT[C/T]GCAGAAGTTAAATTT	9873
rs536742322	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72912555	GATTTTTGCATTAAT[G/T]TTCATCAGGGATACT	9873
rs536743175	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999616	TGAGCCACCACACCC[A/G]GCCTTATCAAACATT	9873
rs536760081	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73112497	AATCTGCTTGGTGTT[C/T]TATATGCTTCTTATA	9873
rs536764701	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124608	TGAAAATACAAAAAT[C/T]AGCTGGGCATGATGG	9873
rs536777655	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72896637	CAAGGGACTTTTAGT[C/G]ATCAATCCAATAAGG	9873
rs536781522	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892832	GATGGTCTCGATCTC[C/T]TGACCTCGTGATCCA	9873
rs536789665	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72846131	CTTGAGACTGAGCGC[A/G]TATGTTTTCCCAGAC	9873
rs536804504	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73105072	CTTATCCTACCTGAC[G/T]TGACAATAACTCTAT	9873
rs536810542	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101664	GTAGTCTGGAACTCC[C/T]GACTTCAAACGATCC	9873
rs536823220	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72962596	GATATGAACTAAATT[-/C]CCCCCTTTTTTTTTT	9873
rs536830004	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73141117	GCCTCGGCCCCTGGG[A/G]AAGCTGGGGAAGGGC	9873
rs536847464	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117386	TGATTTATATTTTAT[C/T]ATTTTTCCATCCTAT	9873
rs536855795	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72885256	ATTATTTTATGCTAA[C/T]AGTAAAATTAATTAA	9873
rs536862038	snp	C/T	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72993414	CCATTACTGGGTATA[C/T]ACCCAAAGGATTATA	9873
rs536870937	snp	C/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:73097616	TCTTGTGAGGTGTTC[C/T]TTTTTTTTTTTTTTT	9873
rs536872746	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093921	ATGAATGTTAAGAAT[A/G]AAGATAGGACTGGGT	9873
rs536873250	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941809	AAAGTATTAACCAAT[A/C]TTTGTTTTTGACCAG	9873
rs536882780	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72876855	AGCATTATTATTATA[C/T]ATACGTCCAGGATTT	9873
rs536885732	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73018843	ACTATTTTAAGAGAA[A/G]TATGTGTGGGTATTC	9873
rs536891878	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042119	TTTAGTAGAGACAGG[G/T]TTTCACTGTGTTGGC	9873
rs536902106	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877887	GGCACATGTCTGTAG[C/G]CCCAGCTATTCGGGA	9873
rs536919270	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73017385	ACTTATTTCTATACA[C/T]GTAACTAAAAAGAAC	9873
rs536920803	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73059342	TTGTTTCCTTTTTAA[A/C]AAAGGAATTTTAAAA	9873
rs536922238	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73026297	CAGATAAATGAAATA[A/T]TCTGTATGAGGACTA	9873
rs536934717	snp	G/T	0.00399679	0.0445244	intron-variant	FCHSD2	GRCh38.p7	11:73089971	GTAATTAAAATAGCT[G/T]GGTAATGGAACATAA	9873
rs536937294	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988849	CACATGTAGGTCAAA[C/T]GAAACCACCACTACC	9873
rs536945774	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72988961	AAATGTTAAAACACA[C/T]ACTTTGCCTCGATGT	9873
rs536958271	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031899	TAGATGCTGGGGGAA[C/T]AGCAATAAACATTAT	9873
rs536966927	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132286	CCACTAATAACAGTA[C/G]CTACCAATGCTAAAT	9873
rs536970723	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73049105	GGATGGTGAAGATCT[A/G]ATTTAATAGCAAGAT	9873
rs536975494	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72980706	ATATATAATGTATGT[A/G]TGTATATATATGTAT	9873
rs536996122	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927082	AATTCACAAGCACAA[A/C]ACAAATGTATTTCAG	9873
rs537014460	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110761	GGTACATCATTAGGT[A/T]ATCTAGCTGAAGATT	9873
rs537025108	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010578	TAGATCTATGGTGTT[A/G]TTTGGTAGGGCCCTT	9873
rs537027346	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954458	CGATCCTTCCCCTTC[A/G]GCCTCCCAAAGTGTT	9873
rs537035053	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118225	TTGGGAGGCTGAGGC[A/G]GGAAAATTGCTTGGA	9873
rs537046022	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73087749	TTTAGTGCAGCCTAA[A/G]TGTATAGTGTAATAA	9873
rs537047640	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73090436	TTCACCGTTTTAGCC[A/G]GGATGGTCTCGATCT	9873
rs537051749	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903893	CTACTGCTTCCCTCC[C/T]CCTCACTCCACCAAC	9873
rs537077957	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002462	CAACCAATGGAACTT[A/G]CAATGTAAACTCACC	9873
rs537099358	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72956826	TGATTTCATAGTGGA[-/A]AAAAAAAAAAAACCA	9873
rs537102526	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72972399	TTCTTTCCAAACTAT[A/G]TTTCAAGGTGCCCTA	9873
rs537108060	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73125464	AATCCCAGCACTTTG[C/G]GAGGCCAAAGAAGGG	9873
rs537111698	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72865591	CCCTTCCTTCACAAC[A/G]AGAACAGCCCTTCTT	9873
rs537119549	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73073803	GAAGACCACATAAAA[G/T]CAAATAATAAAAACT	9873
rs537133734	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72865953	TATGAGGAGGGAGAC[C/G]AAGTTTTGTTCATCT	9873
rs537140801	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994845	GCTTTTAAAAAATTG[A/G]CATATAATTCACATA	9873
rs537146791	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73121804	AGTGATTATTAAAAC[A/C]TGGATTGCTGGGCTC	9873
rs537169920	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72922012	TGACATATGATATCT[A/T]CTGCCTATGAGAAAA	9873
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	9873
rs537208541	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858415	AATGTGGTACATATA[C/T]ACCATGGAATACTAT	9873
rs537219545	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73013303	AGAATTTCTTTTACC[A/C]AACTGTCTGCCTGGA	9873
rs537230922	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73041473	GATTTTCATTTCCCT[G/T]ATGATTAGTGATGCT	9873
rs537238949	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73123807	GTGCTGGCCAACTGA[C/T]TCTTACTTAAAAGGG	9873
rs537249544	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72998193	ATTATCTTGCTAGAA[G/T]ATTTTTATATTGTTC	9873
rs537249981	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905902	CGCAATAAACATATG[C/T]GTGCATGTGTCTTTA	9873
rs537253580	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72988063	TTTCACAAGTTGCTT[A/G]TAAGGTTGCTTACAT	9873
rs537265037	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72996546	AATAATTTTGAAAAA[C/T]GTAATAATTCTCATA	9873
rs537272117	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72851088	GCTGGGGCGACACAG[C/T]GTGACTCTGTCTCAA	9873
rs537284292	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004952	TTCCCACCACATTTG[C/T]CAAACTCCTTGTCTC	9873
rs537284682	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034402	CAAACATGCAAAAAC[A/G]TTCCTCTTCCTGAAA	9873
rs537296963	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880942	TAGTACAAGAAAACA[C/T]AGGGGAAATGCTTCT	9873
rs537297128	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889183	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT	9873
rs537302481	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123299	CCTCTCCTGCAGTAT[C/T]TCCTAGCCAAGCCAG	9873
rs537335584	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898472	TCAAAATTCCTAATT[A/C]AAACTATAAAATTCA	9873
rs537343867	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106789	ACATGCTGGACAGGT[C/T]TGTAGCCTAGGAACA	9873
rs537345941	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72977654	CAGTTAGAATGGCAA[A/T]CACTAAAAAGTCAGG	9873
rs537347926	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72997538	TTAAAAGAGACCTAC[A/G]GTAATTCAGATAGTG	9873
rs537367065	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72969923	GGAATAGGGGACTGG[G/T]CTCAGAAAAAGACTT	9873
rs537375965	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72926024	GTCCCTGCTGGCTTG[A/G]GGATATCTGTTCCCG	9873
rs537392309	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72873418	ATTCAGACCCTTTTC[C/G]CATTTTTAAGTTGAG	9873
rs537422359	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143430	GCTCCTTAACAGGCT[A/G]GGTGAGCTCGGCTTC	9873
rs537425530	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028026	TCTGCTGCAGGGGCA[C/G]AGCCCTCATGGAGAA	9873
rs537446855	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935409	AAACAAACTCTTCTT[C/T]TCTGAGAGCAACGGG	9873
rs537450960	snp	G/T	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:73076736	AAAGTAACCAGCAAG[G/T]GATAGCAGGTGGGAA	9873
rs537459780	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072854	CACTAACTTCTTGTA[C/T]AGTATGCCCAAGTCT	9873
rs537466573	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976185	TACAGACAGAGAAAG[A/T]TATATTCAGTATCTG	9873
rs537483012	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72913309	AGTCTCAGTCTGTTG[C/T]CCAGGATGAAGTGCA	9873
rs537487715	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023819	AATGGAATAGTACTT[A/G]GCAATTAAAAGAAAC	9873
rs537490047	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73103942	CTTTTCTTTTGCAAT[G/T]TCTGAAACAAGGTGC	9873
rs537500297	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73020254	GTAGACACTAGGAAA[C/T]GGACTGATGGCTTAA	9873
rs537502928	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977068	TAGCTGGGACTACAG[C/G]TGCCCACCACCACAC	9873
rs537509961	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72971905	TAACTGCAAAGGAAC[A/G]AGAGATAAAAGTTTG	9873
rs537514329	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73068199	AAACCATATCAGTAC[A/C]CCAAATAAATGAAGA	9873
rs537515240	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113890	CCAGAAGAATTCTCT[A/G]TATTACTAGGCAGAG	9873
rs537519645	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72918508	TTATTGAATATGACA[C/T]TGGTTGATGCTATCA	9873
rs537533765	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869589	GTCATCCTTGCATAG[C/G]GGCCATGCTAATCTT	9873
rs537545331	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839382	TAAGCAATATCAGAT[C/T]TGCGAAAAGATGACT	9873
rs537580103	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113260	CAAAATAGCTATTTC[A/G]AATTATCTGTCTGAA	9873
rs537585168	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959925	ATATTTCAATGCACT[C/G]ACCTCAGTCTAACTT	9873
rs537587675	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73084036	ACAGTACTCACCTCA[C/T]AGGGATATTATAAAA	9873
rs537589734	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72956230	TAAACAAGCACATAA[A/G]TGGCAGAGAATAGAA	9873
rs537590518	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72968230	GTAGATGCTCCAAAA[C/T]TACTTTCTGAACAAA	9873
rs537596679	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73009687	ACCCTTGGTTGGTAG[-/T]TTTTTTTTTCTTTCA	9873
rs537598409	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72861651	ATAGAAAGGATAGGC[C/T]GGGCGCGCTGGCTCA	9873
rs537599820	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72866748	TTTAAATGTGCAAGT[A/G]TATTCTCATTAGAAA	9873
rs537603785	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72853691	TTTAAATATGATACC[A/G]AGAGCATAGGCAACA	9873
rs537605924	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908623	TTTTGATTTGCATTT[C/T]TCTGATGATTAATGA	9873
rs537622292	in-del	-/A	0.00121507	0.0246182	intron-variant	FCHSD2	GRCh38.p7	11:73002598	CATTTTAAAATAATA[-/A]AAAAAAATGAAAAAG	9873
rs537623671	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008275	ACCCAGGAGGCAGAC[A/T]TTGCAGTGGGCCAAG	9873
rs537627435	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73117542	AAGTTTGTTTATATA[A/G]GGCATTCATTTTCAT	9873
rs537642501	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73081286	TAAAAATACAAAAAT[C/T]AGAAGGGCATGGTGG	9873
rs537643947	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112658	GTTGGTGGTGGTGTT[C/G]GTGTTGTTGAGACGG	9873
rs537673525	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72947931	TGTTAACATTTTTCA[C/T]GGCACTATAATGGTA	9873
rs537679341	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73109197	GGATAGCTTTGGCTA[A/G]CTATTCTGGGTCTTT	9873
rs537683980	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106284	TGGTGACATAAACCT[A/G]TATCCCCAGCATTCG	9873
rs537686683	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009009	TTGAGAAGCATTTAC[A/G]TAGAAAGGAATGAAA	9873
rs537691420	in-del	-/GGCCCGGGC	0.00318978	0.0398085	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142100	ACCGGGAAGGCTTGG[-/GGCCCGGGC]GGCCCGGGCGGCCCG	9873
rs537699167	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059180	AAAAGTCAACCATTT[G/T]GGATGAAAGCAAAAT	9873
rs537701998	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73119571	CTGGGTGCAGCCTCC[C/G]AAGTAGCTGGGACTA	9873
rs537704135	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73128088	TTTCTCCAAATTATC[A/C]GAAGACTGAAGTGGT	9873
rs537704909	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131623	GCACAAGGATCGCTT[C/G]AGTCTGGAAGGCAGA	9873
rs537725873	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983655	CAATCTAACAAAAAT[C/T]ATGCTAAAATGTCTT	9873
rs537742357	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942867	GTTCGCAGCTTCAAA[C/G]TCTTGGACTTCAGAA	9873
rs537743658	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098583	ACAGTATGGTTAGTT[A/G]GAATAGAATTGATAG	9873
rs537748543	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101976	TCCAAAATCTGCAGG[A/G]TAGGCCAGAAGCTGC	9873
rs537749674	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005879	TGGCTTTAAAGAGTA[A/T]CAATATCCTGACTAT	9873
rs537749854	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950580	TACAATTTGTTGAAA[G/T]ACTATTCTTTCCTCC	9873
rs537759209	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953561	TAAAAAGTCACTCAA[C/T]AAAATATTTATCAAG	9873
rs537759820	in-del	-/CAGGGAGG			intron-variant	FCHSD2	GRCh38.p7	11:72845084	TATGTGACAGCAAAC[-/CAGGGAGG]TAGTACACTTTTAAA	9873
rs537778361	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72899151	TATAGGTAATGCCAT[C/T]AGAAAAATGTCTAGC	9873
rs537783281	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045522	TGGAACCAACCCAGA[C/T]GTCCAACAATGATAG	9873
rs537789001	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73021892	CCAGGCAACACAAGG[A/G]GACCCCTGTCTCTGT	9873
rs537789217	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72981305	AAATATATGCATAAA[G/T]ACTTCAAAGTAAGTT	9873
rs537805965	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72862150	ATCTACAAAAACCCT[A/G]CTGCTAACTTCATAC	9873
rs537806473	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73001415	TATAAAAATTAGTGA[A/C]TATTTCAGACTCTCC	9873
rs537808986	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930310	ACCAATCACAGCTTG[A/C]CAGCTCCTCAAAACT	9873
rs537810098	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72993612	TGTCCTTTGTAGGGA[C/T]ATGGATGAAGCTGGA	9873
rs537850121	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72975095	GTTCCTGGCTTATTT[C/T]ACTTAACATAATGTC	9873
rs537850944	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938873	AATTCATTAGGTTTT[A/C]AAATGGTTTTTGAGT	9873
rs537855130	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72985715	CTGTATGATGTAATC[G/T]TCTCCCACTCTTGGG	9873
rs537862811	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72886003	GGCTGTACCAAAAAC[A/G]TGCTCATATTCTCTA	9873
rs537864910	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72896311	GGAAACCTGAGGAAG[C/T]TTCCGTGTTTTTCCT	9873
rs537869148	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840069	ATCTTGCCACCACTT[C/G]TTTCTTGGATGCTGC	9873
rs537871461	in-del	-/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73111714	AAGGTGATTTTCTCT[-/G]GTGGGGTGTTTTAAT	9873
rs537917130	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923168	ACATTTTGTTTATTA[A/C]TCAGGTGATATAAAT	9873
rs537928274	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72929567	ATGATTTGCTCCAGC[C/T]CCCTGCCTTAAATTG	9873
rs537952296	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024542	TTAGAAATAAGAAGG[G/T]GAAATGAGAATGAAT	9873
rs537983805	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987087	CTTCAGAATAAACAT[A/T]TCCAAAATGAAATTC	9873
rs537994225	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72873310	CTCCAGCCCAGGCAA[C/T]GGTGTGAGACTCTGT	9873
rs538002426	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72914933	AAAATAAACTATCAA[C/T]GGAATAAAAAGGCAT	9873
rs538016060	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932803	CATTCCATCTTCTGT[C/G]TTGAGCATAGGGTTT	9873
rs538023579	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960695	ATCCATTCTGTTAGC[A/C]ACCAGAAAGTTCTCT	9873
rs538033126	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061711	GGGAAGTTCGAACTG[A/G]GTGGAGCCCACTGCA	9873
rs538033149	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73025518	GGAGGAGGGAGATAA[C/T]GAGAAAAAAATAACT	9873
rs538060085	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73043028	ACTTTCTCTTTTCCT[A/T]TTTAGATGCCTTGAA	9873
rs538103092	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73017386	CTTATTTCTATACAC[A/G]TAACTAAAAAGAACA	9873
rs538106429	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054062	GCAAATTCTAGCCTG[C/T]TGTCTGTTTCACTAA	9873
rs538108245	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72953028	AAAATTTTGTTACTG[A/C]AAGTGCAAAGAATAA	9873
rs538111179	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961793	TATTTTATAGAATTA[C/T]GTAACTTAGTTTATA	9873
rs538121894	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72936786	TTTTATAATTTGTAT[C/T]AAAGATGATATTCTT	9873
rs538124036	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916286	TTTAATTTCATTGAC[C/G]TTTTGGTACACAACT	9873
rs538140660	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109763	GTGACAGTGGGCATC[C/G]TTGCCATGTTCCAGA	9873
rs538149213	snp	A/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72945668	GACAAAGGGCTAATA[A/T]CTAGAATCTACAATG	9873
rs538172606	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054939	TTAGTCCATTCTCAC[A/G]CTGCTAAATAAAGAC	9873
rs538179410	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73063236	TACAGACAAGCAAAT[G/T]CTGAGGGATTTTGTC	9873
rs538180041	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72846811	AAAATATGCATAATT[A/G]AGCTCTTACGGTACA	9873
rs538194429	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73071788	TTTCTTGTCTTGGTG[C/T]CCACAATTATAAAAT	9873
rs538195524	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839216	TTTCAGTGTGTCTTG[G/T]GTAGAGAGTTACAAA	9873
rs538204236	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004823	CTACATTTCCTTAAT[C/T]CATTCTTCACCCACC	9873
rs538219218	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106110	GAGGCCAAAAGTAAA[C/T]AATTAATTTTACAAA	9873
rs538247381	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73050460	AAACATATATGGGAC[A/G]GGTCACCTTTATCAC	9873
rs538255842	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73113058	GTGCATTTCCAAAGA[A/G]TTTATCTTCAAGCTC	9873
rs538260106	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72994181	TTATTTCCATTAATG[A/C]TAGATGCTTCCCTAC	9873
rs538263220	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72898320	TAAAAGTCCTATAAC[C/T]TTCCTAACTATATCT	9873
rs538266907	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73095137	AAATTAGAAGTGTTC[C/T]TATTTCTTATTAATT	9873
rs538274291	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997520	AAGAAAAACCGCAGG[C/T]GGTTAAAAGAGACCT	9873
rs538279078	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72939542	TTTCTTGGTTAGAAT[G/T]TGATCACTGAGAAAA	9873
rs538289411	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142233	CGCAGCCGCGTTGTC[C/G]GCGCTCCCGGTCGGC	9873
rs538292265	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942680	TACTTTATTAAAATT[A/T]AAAAGTATTGACAAA	9873
rs538299952	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72889574	AAAATTTAGCCAGGC[A/G]TAGTGGCATGTGCCT	9873
rs538306150	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042747	TCATCAGTGTTTTGC[A/G]GTTTTTTGTTGTAGG	9873
rs538328376	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73087317	TTTAAGCTAAATGCT[A/G]TTTCAAAAGTCAAAA	9873
rs538329554	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72986400	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	9873
rs538332936	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938953	GTAAGGATAGGGTCA[C/T]AGAAGTTTTGGTCTT	9873
rs538342739	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73137136	ACCTCCTTCCTCAGG[C/T]AACTGAAGTTATCAT	9873
rs538349567	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989783	AGTATCCAAAGGAGA[C/T]TGACCCCACTTTGAA	9873
rs538352718	snp	A/G	0.000681962	0.0184531	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73141908	TCAATCCTCCCCGAC[A/G]GCAGCGTTAGCAAGG	9873
rs538360465	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932205	CAAACCCAACCCCTC[C/G]TCCTGATCTCCACAG	9873
rs538371021	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72978167	GGCCTGTCATGGGGT[C/G]GGGGGAGCGGGGAGG	9873
rs538376760	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879100	TGTGCGACAGAGTGA[A/G]ACTTTGTCTCAAAAA	9873
rs538391516	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087869	CTAAGCTCCATTCAT[A/G]GCAAGTGCCCTACAC	9873
rs538394421	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882239	TGAGGTCAGGAGTTC[A/G]AGACCAGCTTGGCCA	9873
rs538400112	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72927717	CACAGTTACTTTAGC[C/T]GACTAGGTTGAGCAT	9873
rs538411213	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72871221	TCTGTGACAGCTTCT[A/G]CTTCTACTAGTCCTC	9873
rs538429743	snp	A/C/G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73105192	TAGCTCTGGTTAGGT[A/C/G/T]GGGGGAAGACTTAGG	9873
rs538431746	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72875352	AATATTATAAACTCT[A/G]TCTATCTATCTAGCT	9873
rs538432771	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73036337	GACAAAAAAAAAAAA[A/C]CCAAGCTTCATAATC	9873
rs538437034	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73127155	TATATACTCCAACTT[C/G]TTTCTGTGGAACCAC	9873
rs538457053	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72978967	GTTCAAGCGATTCTC[A/G]TGCCTCAGCCTCCCT	9873
rs538459213	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969402	TTTGCCACCTCAGTT[A/C]ATTTTTTAGAGTATG	9873
rs538470774	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083654	CCTTAAGCCACGGAA[A/G]AGAAGTATACCTAGA	9873
rs538490626	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72877471	GCTTTGGGTCATTTT[A/C]CAGCTCTATTAAATA	9873
rs538495859	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73081815	TTGAAAGGATCAAAC[C/T]AGATAACATATATAA	9873
rs538495899	snp	C/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73126317	TGCACTCCAGCCTGG[C/G]CAACAGGGCAAGATT	9873
rs538501968	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:73084879	CCTGAGTTTAAAGAC[-/TT]TACCGTTATGTGCCA	9873
rs538504727	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73074602	ATATAAAAGAAAAAA[A/T]ATATATTTCCTTAAA	9873
rs538509520	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73134992	TAGAGTAGCTAGGAT[C/T]ATAGGTGTGCGCCAC	9873
rs538514148	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73121193	CACACACACACACAC[A/G]CATGCACGCACACAC	9873
rs538524654	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72919873	ATAAAAATGTCACCC[A/T]ACCACATATTCCAAC	9873
rs538541911	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018501	CTCTATAAGCTCCAT[C/T]AGGTACAGATCTTGT	9873
rs538553497	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73118222	AACTTGGGAGGCTGA[A/G]GCAGGAAAATTGCTT	9873
rs538561328	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72943311	ACTTTTATATTTACT[A/G]TCTACATTTAACACT	9873
rs538572341	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962555	AGTGATTTTTGAGAT[A/G]TTTTTCTTCAACCAT	9873
rs538585938	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863866	GGAACAACTGAAACA[C/G]TAGTACCCCGTTGAT	9873
rs538586369	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72996754	CAGACTACCTTTCTC[C/T]AGACTGGAAAGTGTA	9873
rs538589370	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066712	AAGAAGACATTTATG[C/T]AGCCAACAGACATGA	9873
rs538600133	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73097885	TGCTATGTTATCCCA[C/G]TTGGGCTTAAACTCC	9873
rs538602078	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72989790	AAAGGAGATTGACCC[C/T]ACTTTGAAACAAACC	9873
rs538603053	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965785	GCATGTTCTTAAGTA[C/T]ATAAATAGAATCACA	9873
rs538623642	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913141	CAAGGGGGAACTCCA[A/T]CCCCGTGATTTAATT	9873
rs538625295	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941967	TGGCATATTAATATG[A/C]TCAAATACTATGCAG	9873
rs538633517	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72989095	TGTCAACTGGTCCAC[A/G]CACTGTAAAATACAA	9873
rs538636207	in-del	-/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72925747	TGCTGCCATCATGCC[-/G]GCTAGAGCAGGGAAG	9873
rs538637090	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949477	AGAAAAGAAAAGAAA[A/G]GAAAGAAAAAGAAAA	9873
rs538642314	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958150	GTGTTCCCACTATTT[C/T]ACAAAGGGGAAAGAT	9873
rs538650356	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067297	GAGAACTCATGGACA[C/T]AGGGAGGGGAATATC	9873
rs538662232	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72906930	TCGGTTCCATATGAA[C/T]TTTAAAGTAGTTTTT	9873
rs538680533	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72866027	CTGCTCAGTTCAAAG[G/T]CAGATGGTATATGGC	9873
rs538695229	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141330	TTTTCCCTTGGGGTG[G/T]GGAGGCGGTGACTAT	9873
rs538715150	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73060225	TAACACCCATTCAAG[A/G]AAGTTTAAACAAATG	9873
rs538719176	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950781	AGATATTTAGAGGCA[A/G]CACAGGTAGTAGTTG	9873
rs538721895	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091119	TTTATGGCTGAATAA[C/T]GTTCCATTCTATGAG	9873
rs538754145	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73107522	ATTGTCACCCTGTTG[C/T]GCTATCAAATACTAC	9873
rs538758722	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943595	TGAAGGGCACAGAAA[C/T]GGAAGTGAGAATTCC	9873
rs538773321	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73082941	TAATCTGGACTCCAC[G/T]AAAGGTCTAAGTAAA	9873
rs538775805	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044848	GGCCGAGGCAGGTGG[A/G]TCACGAGGTCAGGAG	9873
rs538786680	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73052243	CTATGAAAAATTATA[A/G]GTCAATAAACATGAT	9873
rs538796613	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844502	CCTGACAGCAGCAAT[A/C/T]CACCAGCATCAGCCA	9873
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	9873
rs538852904	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044347	CTTTGGGAAGCCAAG[A/G]TAGGAGTATCGCTTG	9873
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	9873
rs538868612	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092724	ATCTACATCCACATG[A/G]ACCAATCAAGTTTCT	9873
rs538870730	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021420	CAGGGGCGTGGATGG[C/T]GCTGGAGGCTATTAA	9873
rs538881241	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991328	AACTATTCCAATCAA[C/T]AGAAAAAGAGGGAAT	9873
rs538884743	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72965359	GAATTTTTACTGAGC[A/G]CTCTTCTATGCACTA	9873
rs538888695	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875604	GGCCTCCCAAAATGC[C/T]GGAATTAGAGGTGTC	9873
rs538904335	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72912506	TAATCTTTTTAATGC[A/G]TTGTTGAATTCAGTT	9873
rs538935248	snp	A/G	4.36157e-05	0.00466969	intron-variant	FCHSD2	GRCh38.p7	11:72867842	GAAAATCAACTTGTC[A/G]TATCCAAGAAAAGAA	9873
rs538935439	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858703	TGAAATAATCTGTAC[A/G]ACCCCCCCATGACAC	9873
rs538938176	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134287	ACCAGCTGGGGCAAC[A/T]TAGTGAAACCCTCTC	9873
rs538939875	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983535	GCCAAAATTGTAGTT[A/G]ATAAAAAATTCAGGC	9873
rs538951833	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72865334	TCCTCATTAAGCTAT[C/T]TTGTGCCTATGTCTC	9873
rs538963585	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72930480	TAATTGGCTGGGTGC[A/G]GTGGCTCACACCTGT	9873
rs538975169	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73119471	CTATGATGACAGATT[G/T]GTTTTTTAATACATA	9873
rs538978545	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72975060	TTAGCCAGAAAAACC[A/G]AAAAAGAACTTGGCT	9873
rs538989859	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117458	AGATGAACCCACTAC[C/T]TTTCAATCTGTCCTA	9873
rs538995051	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085532	TCTCTTTTTCCCCTT[C/T]TGAGAGCCAGATCTT	9873
rs539003681	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141802	AGCGGTCGCCCCAGC[C/T]GCGTTCCGCGTACGC	9873
rs539005121	in-del	-/GTAC	0.31357	0.241783	intron-variant	FCHSD2	GRCh38.p7	11:73035202	TATGTATGTATGTAT[-/GTAC]GTACTAAGACAAGGT	9873
rs539025049	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72872865	CCATCTGGGGAAATA[C/T]TAGACTGTTTTTCAA	9873
rs539029487	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73074921	TGTCCCAAGGATGGA[C/T]GGACAGACAGTGGGG	9873
rs539050431	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062582	AGAATAACCAGTGTA[A/G]AGGAGAACATAAATG	9873
rs539067960	snp	A/C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73006097	TTTAAATAAAAATAG[A/C/T]ATCTCACTTTGTTGC	9873
rs539088891	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72854059	CTGTTATATATATTT[C/T]TAAAAACCCAGAAAA	9873
rs539095837	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959034	GTGTGTGTACATCCA[C/T]GCGTGCATGGGACAC	9873
rs539098510	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110068	AATTTTCCTTTAATG[C/T]ATTATTGAGTTCAGT	9873
rs539103385	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73107860	TGCTGATGGACACTC[-/A]AGGTTGCTTCCAAAT	9873
rs539118011	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72901771	AATATTCTAAGAAAT[A/C]TGAAAGGAATTATAA	9873
rs539120144	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998414	AGGTGTGGTGGCACA[C/T]GCCTGTAATCCCAGC	9873
rs539129341	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006730	TTGGCATATATGTTT[A/G]ATTATTCACTTGTTT	9873
rs539141703	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73104919	AATCTATATTTTACA[A/G]TATAGTTTTACACGT	9873
rs539142897	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909806	CTGCCCGGCCGCCCC[A/G]TCTGAGAAGTGAGGA	9873
rs539158499	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946298	GACTATCGCAAGGAC[A/T]AAAAACCAAACACCA	9873
rs539160383	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890665	CTATGGAAAGTGCTT[C/T]ATATAACTTTTTTTT	9873
rs539163722	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852586	CGAGAATTGCTTGAA[A/C]CTGGGAGGTGAAGGT	9873
rs539175784	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72845193	TGGGAGGCCAAGGTG[G/T]GTGGATCACTTGAGG	9873
rs539210139	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73012830	TTTGTCTCAGAACAA[A/C]TTTGACAAACACAAA	9873
rs539228777	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73014389	CCACCTCGGCCTCCC[A/G]AAGTGCTAGGATTAC	9873
rs539233813	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73112566	TCTGTTGTTATCCCC[A/G]TGAATAAACTTTCTA	9873
rs539243151	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947020	CTCCTTGTGTCCCAG[C/G]CTGCTTTCCCAGGCC	9873
rs539246298	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100513	GGATTACAGGCATGC[A/G]CCACCACGCCTGGCT	9873
rs539248194	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891690	AATAGGTTTTTGAGT[C/T]AGATAGACTTAGTTT	9873
rs539250065	snp	C/G	0.02016	0.0983543	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143170	TCCGCTGAGAGGGAG[C/G]CAAGAGAACGTTAAG	9873
rs539273806	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104458	GATTTTCAGTAGAGA[C/T]GGGGTTTCACCATGT	9873
rs539275786	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096338	TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	9873
rs539291451	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72949058	CACACACCATTAAGT[C/T]AATCATTTTAAAGTA	9873
rs539291750	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73045945	AAAAATGGAAGGAAA[A/G]CAAAAAACATCTCTT	9873
rs539298585	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037406	AGTTATTTTCACTGC[C/T]CTAAAAATCCCCTGT	9873
rs539302097	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991939	GAGAAGGAAATAAAG[A/G]GTATTCAATTAGGAA	9873
rs539315785	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047917	TTATTAATCCCAATA[C/T]GCAGAGGGGGAAATG	9873
rs539333853	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72995357	ATAATGCTGTGTTTG[C/T]AGGTGTGAAGAGCTA	9873
rs539338110	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096658	AAAGGTGCATCCTTG[G/T]GTTCTTCCTGAACTT	9873
rs539341086	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937634	AGGCGTGAGCCACCG[C/T]GCCTGGCCAAAATAT	9873
rs539342205	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987354	TTTCTAGGCTTTCCT[A/G]AAAGTGTTTTCACAT	9873
rs539351744	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73071100	TACTAAAAGATGGTC[C/T]ACCAATTATTTTACA	9873
rs539360588	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73065020	CATGAGGCCAGCATC[A/G]TCCTGATACCAAAGC	9873
rs539362833	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038122	GACGAGGTGGGAAGA[C/T]TGCTTGAGGCCAGGA	9873
rs539372352	snp	A/C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940960	TGGATCACCAAAGCA[A/C/G]TCTATAAGCACAGGG	9873
rs539375031	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73079259	TGGAGTGTGGTGGCC[A/T]GATCTTGGCTCCCTG	9873
rs539380841	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72979128	CTCCCAAGGTGCTGG[A/G]ATTATGGGTGTAAGT	9873
rs539386184	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915732	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	9873
rs539386411	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72888457	GGAGGTGAGATTCTA[C/T]AGATAATAAGCATAG	9873
rs539400449	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961536	GCTATGATTACAGGC[A/G]TGAGCCACCATACCT	9873
rs539409174	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72922218	TTAGAGACAAAATGC[G/T]TGGGTTCTGATCTTT	9873
rs539412430	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73017323	TGGTCCCCTAACACT[A/G]TAACAGGGCCTAATG	9873
rs539422421	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909451	CAGCCTCTGCCCAGC[C/T]GCCACCCCATCTAGG	9873
rs539433107	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73013832	AAATAAACTTGGAAT[A/G]TAACTCCTGGCCTCA	9873
rs539447303	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72999900	ACAAACACACACACA[C/T]ACACACTTTCTTCCA	9873
rs539462885	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73050580	AGGAACCCAGGCCCC[C/T]ACAATGGTTTTTCAG	9873
rs539466911	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72980061	TTTAGACAGGAACAA[C/G]TGCTACTGAGACTCT	9873
rs539467502	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73018372	GTCTTTTTCTAAAAC[A/G]CCTTTTCTAATCACT	9873
rs539470227	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72962016	AAGCATTGTTATTGA[A/C]ACCTAAGAATTCCAT	9873
rs539474210	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880786	GTGGGAGGATCACCT[C/G]AGCCTGGGGAGGCCA	9873
rs539491704	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72989672	TACACATATACATTC[A/G]AGGAGAAGGGATGGA	9873
rs539496497	snp	A/C	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72855320	AACAAACAAAAAAGA[A/C]CAAAAAGTTGCTGGG	9873
rs539509495	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72873344	AAAAAAAAAAAAAAA[C/T]GAATCTTTTCATGTG	9873
rs539528816	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081924	AAAAGCATTCAAGAT[C/T]GGGCGCGGTGACTCA	9873
rs539530614	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903012	TCCCAGCTCTAAAAT[C/T]GTATGGGCCTCTTAA	9873
rs539532537	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73010531	CTTCCAGTTTTTTGA[A/T]TTTGCTTCTGTAGGG	9873
rs539533057	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72994759	TGACAGAGCGAGACT[C/G]CATCTCAAAAAACAA	9873
rs539560771	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73027796	TGCAGCCTTGGGACA[C/T]GGTGCCCTGCACCCC	9873
rs539567932	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894959	AATCTGGAAAATTCT[G/T]AATTTTGACATGTAT	9873
rs539593531	snp	G/T	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72991959	TCAATTAGGAAAAGA[G/T]GAAGTCAAATTGTCC	9873
rs539613510	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011470	AGTGTTAACCCACAG[C/T]TTGGCCCCAAGGGCA	9873
rs539614568	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903685	CTACCATATCGCTTA[A/C]CCCTTACTTGTCTTT	9873
rs539616130	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73020182	TTGTTTTACCTCTCA[A/G]TAACACTTGCTGTAT	9873
rs539623543	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73099326	CCAGGATGTGAAGAA[A/C]TTAGAACCCTCATGC	9873
rs539625488	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144248	AGGCCAGGCGCGGTG[C/G]CTCACGCCTGTAATC	9873
rs539636312	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141282	CTCGCCCCTCAGCCG[C/G]GGACGAGGCAGGACC	9873
rs539638875	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994753	CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA	9873
rs539648781	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911416	GAAGTCACACAATAT[C/G]ATTCCTTGAGTTCTT	9873
rs539652286	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940463	AAATAAGCTATTTTC[C/T]TTTCTGTCTGGCAGT	9873
rs539709326	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115134	CCCTCTGACTATGGC[G/T]GGCCTAAATGCTCCC	9873
rs539718449	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72887740	TATAGACTTACTAGT[A/C]ACAAACTTACTACAG	9873
rs539723035	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72857638	TTTTTTAGTAGAGAC[A/G]GGGGTTTCACTATGT	9873
rs539732032	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72967863	TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT	9873
rs539748684	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73133353	AATAATAGTAAAAAG[G/T]AGAAACAACCCATAT	9873
rs539749155	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114258	CTACTGCCAATGTTC[A/C]CTTCAGGCTCAAGTG	9873
rs539757430	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880055	GCTACCCAAACCAAA[C/T]CAAAACAAGACAAAA	9873
rs539766303	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041354	CCTACCAACAATGTA[C/T]AAGAGTTACCTTTTA	9873
rs539771295	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897432	TAGCATAGCATTTAC[A/T]TTGTATTAGGGATTA	9873
rs539772183	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121816	AACATGGATTGCTGG[A/G]CTCCACTCTCAGAGT	9873
rs539773691	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088796	TTCACCATTTAAAAA[A/C]CTCTAAAAAGCCTAT	9873
rs539782166	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850264	GAGATGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG	9873
rs539792834	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73004342	ATAGCACCTCCATGG[C/T]CATAACCTAGATTCT	9873
rs539792940	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72966225	AGTGCAGTGGTGCGA[C/T]GTCGGCTCACTGCAA	9873
rs539796980	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72925037	TGAGTTCAGCAAATG[A/G]TAATACAGGCATCAT	9873
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	9873
rs539825660	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021530	CATGAACACATAGAG[A/G]AGAACAACAGACACT	9873
rs539830431	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034276	ATATATTTACAGATA[C/T]GTTAAAGTGGAATTT	9873
rs539870164	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73027464	CTTTTTCTGAAAGCA[C/T]ACAGTCATATCCAGT	9873
rs539870271	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72867437	AGTCACCTTCAGACT[A/T]AGCCCACGTACTAAG	9873
rs539883238	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925692	GTAGACACGATTATC[A/G]AAATGGCTGCCAAAG	9873
rs539888308	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022438	AATACAACGTCAATA[C/T]TCCAAAGTTAATTGC	9873
rs539904169	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72957247	GTCCATGTGATCTCA[C/T]TGTTCAATTCCCACC	9873
rs539918488	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72906473	TGTTGCCATTGCTTT[C/T]GGTGTTTTAGTCATG	9873
rs539918962	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72917024	GAGTGTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	9873
rs539926652	in-del	-/TTAA	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73130696	TGTGACAAAAAAAGT[-/TTAA]TTAAACAGACCCTCT	9873
rs539930198	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73019478	TTATGAAATTAATTT[G/T]TTAACTTTGTGCATT	9873
rs539938822	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73025687	TTTAAAAATTTTTTA[A/T]ATCTCCTTGGAATTA	9873
rs539944349	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014843	ACCTCAAAAAAGAAA[A/C/T]CAAATTCTTTTTTTT	9873
rs539955833	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72937143	ATAGCTGGAGGAAGA[C/T]AGAGCTAGAGGACCA	9873
rs539955932	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143599	TGCCCAGGGAGGTTT[G/T]TTTTTTTTTTTTGAG	9873
rs539974737	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73081213	GGCCGAGGCAGGTGG[A/C]TCACAAGGTCAAGAG	9873
rs539976455	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73131506	TGCACTCCAGCCTGG[A/G]TGACAGAGTGAGACT	9873
rs539991232	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910392	TCGAAAAGAAAAGGG[A/G]GAAATGTGGGGAAAA	9873
rs539993940	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059803	CTCATCCCAAGACAA[C/T]GAAAACCCACGGTTA	9873
rs540005083	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135965	CCCAGGAGTTCAAGA[C/T]GAGCCTGGGCAACAA	9873
rs540007823	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72917623	GAGTGCAGTGGCTGA[C/T]GCCTGTAATCCCAGC	9873
rs540007880	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72857407	TACTAACGTTTACCC[C/T]TTCTTAGATGTTGTA	9873
rs540020710	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73006311	CCTTTACACCTAACA[C/T]GTACAAAACTAAATT	9873
rs540024386	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955278	GGAAACATTTTATTT[A/G]TACTTACTCATTTAT	9873
rs540027946	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72904888	GGGAAGAAATGACAA[A/T]CATGTAATTTTTATT	9873
rs540061134	in-del	-/AAAAAAAAAAAAAAAAAA	0.381308	0.21274	intron-variant	FCHSD2	GRCh38.p7	11:73126340	GCAAGATTCCATCTT[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAATT	9873
rs540062237	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143272	AGGACTAGAATCTGC[G/T]TCAGGAAGTGTTCTA	9873
rs540071635	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72854183	CATGTTTCTTCAATA[A/C]ATTAAACACAGAATT	9873
rs540083734	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998544	AGACTCTGTCTCAAA[A/G]AAAAAAAGTTAATTT	9873
rs540084868	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72899672	AGCCCAGGAGGTTGA[A/G]GCGCAGTGAGCCGTG	9873
rs540092774	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73057783	CAAACAATGTATTGC[A/G]CCCCACAGCTATACA	9873
rs540116730	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73132649	ACAACATGGCAAAAC[C/T]CCATCTCTACAAAAA	9873
rs540121267	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900454	GATTTAGGGCTGCAG[C/T]TGGGCTGGGAAAAAG	9873
rs540124388	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:73105404	ATAAGACACCACCAT[A/G]CCCCAGAATCTACCA	9873
rs540126967	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943768	AATAAGATACATAAA[C/T]ATTGTATTTTGATAT	9873
rs540141432	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72890903	ATTAGGAATTTTTTT[A/T]AAAATATAAATTACC	9873
rs540148569	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949082	TAAAGTATACAATGC[A/G]GTGGCTTTTAGTATA	9873
rs540159314	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73049136	ATGTAAAAAGACGTA[A/G]TGGTTTTTGAGTTTG	9873
rs540167154	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936800	TCAAAGATGATATTC[C/T]TTATTTGCTGAGATA	9873
rs540169878	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73054706	TTCAGACAGAGTCTT[A/G]GCTTTGTCACCCAGG	9873
rs540171881	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044619	TTCTATTAATCTACA[A/G]TAATAGAATTCAAAC	9873
rs540176923	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73084054	GGATATTATAAAATT[C/T]AGTTACTTGAAATAC	9873
rs540181666	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73101166	CCTGAGGTTTAGTTC[C/T]GACCTGAAGGAGAAA	9873
rs540192638	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074212	TGGAGTGCAGTCAGG[A/G]GGAATAAACTTTTCA	9873
rs540197933	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72888987	ATTGAGACAGAGTCT[C/T]GCTGTCGCCCAGGTT	9873
rs540210590	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029367	TGCAATTATTTTAGA[A/C]TTCTAGAAGCCACTG	9873
rs540211056	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73061301	TGTCGCATGGTTTTC[A/G]CAAACTGCAGACCAG	9873
rs540227605	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72955920	CCCACTACGGACTCA[A/C]AGTAATAGCACACAG	9873
rs540233680	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72928537	GATGGTTAACACAGG[A/C]AACTGACATTTACTA	9873
rs540236258	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72861357	CCTTAATAACCCTGT[A/G]TCTACTAAAGAAATG	9873
rs540244274	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974074	GACAGGTAAGGGCGG[A/G]GGGCGGGATGGAAGA	9873
rs540251415	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066313	CAGAAAATTGAAACC[A/G]GATCCCTTCCTTACA	9873
rs540251468	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075010	CTTTAACAGGCACTT[A/C]ATAACACAAAATATT	9873
rs540260318	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72929921	TAATAAATGATTATT[A/G]AAATGAATCAAACTG	9873
rs540266730	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920262	GGCACACACAATATT[A/T]AAAACAAAAACAGAG	9873
rs540270234	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73095146	GTGTTCTTATTTCTT[A/T]TTAATTAGGTGACCT	9873
rs540279475	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72966157	TTTATTATTCTTCTT[G/T]GAACTGAGCCTTTTT	9873
rs540293011	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72957601	AGAAATAAAAAAGAT[A/G]TTTTTGGAACATCTC	9873
rs540294849	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966456	TGAACCACCACACCC[A/G]GACTAAACTGAGCAT	9873
rs540294924	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72924287	AGCTATTTTTCTTTC[-/T]TTTTTTTTGAGACAG	9873
rs540303537	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913393	CACACCTCAGCCTCC[C/T]GAGCAGCTGGGATTT	9873
rs540331289	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030669	ACCAACAAAGAAAAA[C/T]ATATTAATAGTACTG	9873
rs540331771	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851507	GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC	9873
rs540345138	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921521	CCCATGTGAGCAGAG[A/T]GCATTTAAACTCTGA	9873
rs540348279	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930563	CAGCCTCACCAACAA[C/G]GTGAAACCCCGTCTC	9873
rs540350042	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73014611	AATCATCTGATGTCA[A/G]TCATCACTGACAATT	9873
rs540377480	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73038347	CCCTGTCTCTTTAAG[-/A]AAAAAAAAAAAAAAA	9873
rs540382562	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73076978	AGCCAGGCATGGTGG[C/T]GGGCACCTGTAGTCC	9873
rs540382645	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72922585	TTGAGGAATGATTAA[A/G]CTATGATGTGTACTG	9873
rs540389848	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852031	ATAGGTGTGCACCAC[C/T]ACACCTGGCTAATTT	9873
rs540394990	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73131255	GGGCGCAGTGGTTCA[C/T]GCCTGTAATCCCAGC	9873
rs540406396	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967390	AATGGGTAAACAAAA[C/T]ATGGTATATCCATAT	9873
rs540423917	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73060513	AGAAAGTTTTCCAGG[C/G]GAAATAATCAATAGT	9873
rs540427139	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72914089	GCATAATCTCAGCTC[A/G]CTGCAAACTGCGCTT	9873
rs540436049	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72863493	TCCATAAAAGAAAAA[C/T]TGGTAGGTTGGACTT	9873
rs540445327	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73068595	TGGTTTAAAGTTTTA[A/T]CAGTTTTTATACAGT	9873
rs540456984	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73105559	AGTATCTTTACTACT[A/C]TAAGCCTCAATTTTT	9873
rs540463608	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72997553	AGTAATTCAGATAGT[A/G]AAATTATATAATAGA	9873
rs540472315	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099595	AATGTGGTATATACA[C/T]ACAACCGAGTATTAT	9873
rs540495878	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72897226	ATCCTATTTAATTTT[C/T]AAACAAATAAGGTAT	9873
rs540496251	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861007	ACAAATTAGAAAGGA[G/T]AAAATTAAATCCAAA	9873
rs540498193	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994849	TTAAAAAATTGACAT[A/G]TAATTCACATACAAC	9873
rs540504509	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73141993	TGTGTGAAAGGAGCG[C/T]TTAAGAAGCAAGACT	9873
rs540505708	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73069769	TTCTTTCCAGAATTG[A/G]AGAAAAGCAAGAGAC	9873
rs540525093	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73033779	GCTGTGAATTAGTTA[C/T]GAGTATTCTTGGATA	9873
rs540533792	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099980	ATGTGCCGTTTGTCA[C/T]AGAAGCACTCACAGC	9873
rs540534412	in-del	-/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72922957	CTCCATCCCTTCCTT[-/C]CCCCCAGCCCCTGGC	9873
rs540569057	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960803	TGTGAAATACACTCT[C/G]ATAATAAGAATACAG	9873
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	9873
rs540570757	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72931085	ACCTACTATATACCC[A/T]CAATAATTAAATTTT	9873
rs540571959	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72854865	GAAATGGGCCAGGCA[C/T]GGTGGCTCATGCCTG	9873
rs540576660	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72845302	GGCACGTGCCTGTAA[G/T]CCCAGCTACTTGGGA	9873
rs540581669	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73108792	TAGCCAGGATGGTCT[C/G]GATCTCCTGACCTCA	9873
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	9873
rs540592595	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891941	AAATTACTTGAAACA[A/C]AAATTTTCTTATTAC	9873
rs540609142	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73112087	TATTACCAGTGAGTT[C/T]TGTACCTTTAGATAA	9873
rs540612343	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73053803	GATTCTCTATATTAA[C/T]AGAAGATATCTTCAA	9873
rs540619866	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940555	TAGTCTCATGTCATG[A/C]GCTTTCTTCTGAGAG	9873
rs540629081	in-del	-/ATAAA	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72870554	ATAATAATTTTTAAT[-/ATAAA]AGAACTTCTCTCTAA	9873
rs540637100	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73083361	CGAGACCATCCCGGC[A/C]AACATGGTGAAACCC	9873
rs540657686	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933160	TAGGCAGATATGCAA[C/G]ACAGAACCTCAAACC	9873
rs540659261	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093506	AGAGCTGTCTTAGAA[A/G]AGCTGTAATGCACCC	9873
rs540663119	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73027285	GAGAAGAGGAACTTA[C/T]TGAGAACTAGAGCAA	9873
rs540672682	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119177	CATAGTGGCACATGC[C/T]TGTAGTCCCAGCTAC	9873
rs540681526	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72888112	ATGAGGGTAAAGAAT[A/G]AGAAAACAAGATAGC	9873
rs540699963	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73096843	AAACAAAAAAAAAAA[A/C]GGAAATTTCCTTCCA	9873
rs540719439	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116326	TTTTTACTTATGCTC[C/T]TAAGGCAGACTGGCA	9873
rs540723895	in-del	-/A	0.39214	0.205661	intron-variant	FCHSD2	GRCh38.p7	11:72985358	ATATCCAGAATGACC[-/A]AAAAAAAAAAAAAAA	9873
rs540728577	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72877080	GGCTGCCTCCAGTGC[A/T]GCCTCATCCTCCTAC	9873
rs540732231	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72933682	ATAATAATTCAATTG[C/T]TTTCCTTACTATTCC	9873
rs540743343	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73031200	TAGAGAATAAAGGCC[A/G]GGCACGGTGGCTCAC	9873
rs540744643	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869287	TCCCTCAAATTAATT[A/C]AGTTCTTCCTAATCG	9873
rs540755433	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72976462	TTTTAAATTTTTTTG[C/T]AGAGACAAAGTCTCA	9873
rs540761391	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73010096	TTGTTAATTCTTTCT[C/T]ATTTTTCTTCTTTTT	9873
rs540801960	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134457	CTTGGGTGACAGGGC[A/G]AGACCCTGTCTCAAA	9873
rs540806789	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024048	TGGTGAACTAATATA[C/T]ATAGTATTGTAGTAG	9873
rs540817431	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73134923	TATCTCAGCTCACTG[C/T]AACCTCCACCTCCCA	9873
rs540821692	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72926386	GAGAGGATGGCATGA[A/C]CAGTTGCAGAGAGGA	9873
rs540830015	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72914476	AGAGGCATCACGCTA[C/T]CCAACTTCAAACTAT	9873
rs540840504	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072260	TAATGGGGATCAGCA[C/T]CAACAATGATTTCCT	9873
rs540875362	snp	G/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:73016289	GCCTGGGTGACAGAG[G/T]GAGGCTCTGTCTCAA	9873
rs540884388	in-del	-/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100339	TTACATGCTTTTGTT[-/G]GTTGTTGTTGTTGTT	9873
rs540889168	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963906	ACCCTGGATTAGATG[A/G]CAACTCTGTGTCATG	9873
rs540891469	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72954710	TGGTCAGGAGATGAG[C/T]AGTGTACAAAGAGAT	9873
rs540918860	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141430	CCCGCAAATTTGCAA[A/G]CGGGCGGGGCTGGCG	9873
rs540921205	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854111	TGGAAAAATTGGAAC[C/T]TTTATACACTGCTGG	9873
rs540928209	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72894726	ATGCTCTGAAAAAGA[A/G]TAAGTATTTTTTGGT	9873
rs540936769	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016904	TTTGAATTGAGAAGA[A/C]CATTTTGTTAAGAAT	9873
rs540937053	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008427	GGTGTTTTAATAAAT[G/T]TTCATACATGGTTGT	9873
rs540958348	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72865326	AATATAGGTCCTCAT[C/T]AAGCTATTTTGTGCC	9873
rs540971360	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72955556	GCTAAAAGTTCCAAC[C/T]CTTTAATCATGTTTG	9873
rs540986237	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096480	CACCTGAACACAGGA[A/G]GCAGAGGTTGCAGTG	9873
rs540995727	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72849949	AAATGGTTGAAAGCC[A/G]GAAAAACACTTAAAA	9873
rs540997249	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72989234	TCAGTGTCCTTCAAA[C/T]TGCAGATTAAAATCC	9873
rs541051900	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088516	GAAAGTTTTCTCTGG[A/G]TCATGGTATTATAGG	9873
rs541097494	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004167	ACGGTACTTTGCCAT[C/T]CTACATATCACATGG	9873
rs541107949	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850446	TAGTGGCGTGATCTC[A/G]GCTCACTGCAAGCTC	9873
rs541125018	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988211	CAGTCAGCACACTGA[A/C]CCTGAGTCTCAGCTC	9873
rs541127576	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925373	AAATCCTACTTTAAA[A/T]ATTCCAGCTGGGTAC	9873
rs541128610	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106341	AGCCCATGAAGTCAA[A/G]GCTGCAGTGAGCTGT	9873
rs541130524	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73097999	ATCTAAGGTTTGCCA[A/G]TAAGTTATCTTTTCA	9873
rs541145153	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73054472	TAGTCTCTGTCTCTT[A/G]GTATCCTAAAATTCC	9873
rs541158516	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997176	GCCGAGAGGCCAAAG[A/G]GTGAGCAGAGATCAG	9873
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	9873
rs541180653	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73128779	TGGTGAAAGATTCTG[C/T]AGCATCACTGGAGCA	9873
rs541197477	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72989327	CCTAACAACCATACA[C/T]TGAGAAATAACCCGA	9873
rs541216278	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72916615	CCACTGTGCCCAGCC[C/T]CCTTTGTTCACTTTT	9873
rs541233996	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990062	GTGTTAAGAAAGGAC[C/T]ACAGGGGATGAGACA	9873
rs541235869	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882014	GCTGGGTGTGGTGGC[A/G]GGCGCCTGTAGTCCC	9873
rs541249477	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72873521	AAATATTTTCCCCCA[C/T]TCTGTGGGCTGTCTT	9873
rs541251360	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842029	CGCAAACAAGATCGG[C/T]AAACACGTTCCTTCT	9873
rs541258861	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73138637	TTTTTGAGACAGGGT[C/T]TCACTCTGTTGCCCA	9873
rs541288968	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879873	GCTCAGTGGCTCATG[A/C]CTGTAATCCCAGCTA	9873
rs541296056	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064641	AGTGGTGATATCCTT[A/G]TATCAGTGGTGATAT	9873
rs541297165	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73122752	AAAAGTCTCTATTGG[A/C]CTCTGTGAAATTCAT	9873
rs541313673	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121171	CTCTTATACACATAC[A/T]CATACACACACACAC	9873
rs541323444	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72874783	TAGGATTTCAGTTGC[G/T]TATAAGTTAAAAATT	9873
rs541338210	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72966638	AATACATTCAACAGA[C/T]ATATATGTCAGTTAC	9873
rs541339746	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73129579	ACCCCAGATGGGACC[A/G]TCCAGTTGCAGAAAA	9873
rs541347220	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72910363	AACGGGCCATGATGA[C/T]GATGGCGGTTTTGTC	9873
rs541358903	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72910634	AAGGCAGCATGCTCG[C/T]TAAGAGTCATCACCA	9873
rs541363687	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73026493	TGCAATAAAATTTAT[C/T]TTAAAATAAAAGAAA	9873
rs541382416	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857862	CTCAGCTTCATGGCA[C/T]AATCATGAGGTAGAA	9873
rs541384549	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73003300	ACTTACCTCACAGGG[C/T]TATTTTAAAAATTAA	9873
rs541384964	in-del	-/A	0.390277	0.206936	intron-variant	FCHSD2	GRCh38.p7	11:72880000	GTGAAATTCTGTCTC[-/A]AAAAAAAAAAAAAAA	9873
rs541393169	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72973293	AATCACTTGAACCCA[A/G]GAGGCAGAGGTTGTG	9873
rs541395657	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905191	GGTAATTATTGTCGG[C/G]TTGTAGTTGGCCACC	9873
rs541397006	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72948383	TGAATGTTTCATTTT[G/T]CAACATTTTAGTTGC	9873
rs541403855	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73012910	AAATATCTCTGAAAT[C/G]TTCCCTACAACTTGA	9873
rs541404256	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73108266	TATTAGATCTTTTCC[C/T]ATGAAGTTGTTTAAG	9873
rs541428078	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73007470	TACAAAAAAAATTTT[A/T]AAATTAGCCAAGCAT	9873
rs541431846	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861747	CCAACCTGACCGACA[C/T]AGAGAAACCCTATCT	9873
rs541438935	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72944563	AGGGCAATCAGGCAG[C/G]AGAAGGAAATAAAGA	9873
rs541444357	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951822	TTCTTAATATCTAAC[C/T]GAGATCAATCATGCT	9873
rs541464083	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72896987	GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA	9873
rs541465767	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73108742	CCCGGCTAATTTTTT[G/T]TTGTATTTTTAGTAG	9873
rs541483596	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905659	TGTTCTCATTGTTCA[A/G]CTCCCATCTATGAGT	9873
rs541503976	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72981672	TGAAGCACTATGTAA[C/T]ACCTAATACGATACT	9873
rs541505432	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72900664	AAGTCATTGGCAAAA[C/G]CTGATTTGATTAAAA	9873
rs541508594	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72845740	TATAGGTGTTCTTCC[A/G]TCCATCAGGCTCTGT	9873
rs541509569	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122467	CAAAGGTAACACCAC[C/T]TAACCATCTTCTTTC	9873
rs541512046	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73049379	TGACAAGAAACAAGA[C/T]AGGTAAAAGGTTTAA	9873
rs541513023	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000073	TAACATTTTACATAA[A/G]GACACATATACATCT	9873
rs541519758	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72917014	TTTTGAAGCAGAGTG[C/T]TGCTCTGTCGCCCAG	9873
rs541529150	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109302	GCATTGAATCTGTAG[A/G]TTGCTATAGAAACTA	9873
rs541538838	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72850205	ATAGCTGGGATTACA[A/G]GCACCCACCACCACA	9873
rs541539263	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115384	GAGATGGGGTTTCAC[C/T]GTGTTAGCTAGGATA	9873
rs541540547	in-del	-/A	0.499424	0.0169631	intron-variant	FCHSD2	GRCh38.p7	11:73039517	AGAGACTCCGTCTCC[-/A]AAAAAAAAAAAGAAA	9873
rs541563560	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73050712	TTAAAGTCCCTTTAT[A/G]TTGGTTGAACGTTAT	9873
rs541568066	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997761	GCTGGAGTGCAGTGG[C/T]ACGATCTCGACTTCC	9873
rs541571275	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130172	AGCCACCGCGCCTGG[A/C]CCATAATCTCTTATA	9873
rs541571862	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846331	GATTACAGGTGCACA[A/C]CACCATGCCTGGCTA	9873
rs541575554	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73042239	TGAGATTATTTTTAA[A/T]CTCTGGTGAAAGACA	9873
rs541576359	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72992505	CTACCTGACTTCAAA[A/C]TATACTACAAGGCTA	9873
rs541576845	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73090477	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	9873
rs541609609	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035239	GCTCTGTCACCCAGG[A/T]TGGAGCGCAGTGGCG	9873
rs541612099	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73000826	GCAGTTAATAAAACA[C/T]AGTACTTAATGAGAA	9873
rs541616682	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73088103	GTCCTGAACTCCTGG[C/G]CTCAAGCAATCCTTC	9873
rs541618649	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73060775	TGAAGTTAGAAATAC[A/G]CAAAACTCTAGGTTA	9873
rs541625697	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889772	AAAACTCAGTTCCTT[A/C]AACTGTTTGACATTT	9873
rs541628263	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093742	AAGTAGCTGGGATTA[C/T]AGGCATGCACCACCA	9873
rs541637150	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945755	TGAACAGACACTTCT[C/T]AAAAGAAGACATTTA	9873
rs541642565	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042894	CTACTGATTTTTGTA[C/T]GGTGATTTTGTATCC	9873
rs541662887	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73090030	GTAATCAGGAATATA[C/T]CTAAATATATCTACA	9873
rs541666894	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893931	GCTCTCTCAAGATAT[C/G]ATTTTGTTTTATTTT	9873
rs541672478	in-del	-/TATG	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72883055	AAGGTAATGGGAAAA[-/TATG]GCATACTCTTTAAAA	9873
rs541676121	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927403	GGGGTGATGATGATG[C/G]TGTCAGTGTAGGTTC	9873
rs541686542	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73085586	ACCACATTTAAGGGA[A/G]AAATTGAAAAGTCAC	9873
rs541715991	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886094	CTGGAGTTCTAAGGG[A/G]GTGTTAGAAAACCAT	9873
rs541728684	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72883192	TAGAAATGTTTAGGA[C/T]CACAGTCCACAAAGA	9873
rs541749339	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72909234	TGGAGACGGGGTTTC[A/G]CCCTGTTGACCGGGC	9873
rs541755217	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72878698	AGATAAAAATCTATA[A/G]TAAGTTGAAATGATG	9873
rs541764264	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927964	TTTACTTACTTTATC[A/T]TGTTAATGATTTTCT	9873
rs541792498	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123400	GTAACTCCTGGAAAA[A/G]TAGCGCTCATCCTTA	9873
rs541803180	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908217	TGACAGGATCTCATT[C/G]TTTTTCATGGCTGAA	9873
rs541813622	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087447	TGTGGTGGCTCACCC[C/T]GTAATCCCAGCATTT	9873
rs541834112	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032926	GCTTGCGAGCAGTGC[A/G]GTGCCATTATCAGAC	9873
rs541835306	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73008392	GAATAATTTATATAA[A/T]AACTAGTAACAAGAA	9873
rs541862051	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952481	AGGCATGTGTCACCA[C/T]GCCCAGCTAATTTTT	9873
rs541873159	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73070102	GAAACTTATCAGTAA[C/G]AAGAATTTCATTGTC	9873
rs541890553	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901278	GGTGCGTGCCTGTGG[C/T]CCCAGCTAATCGGGA	9873
rs541892771	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131014	AATTGAGAAGCAACT[A/G]TGATTGTTGAATGAA	9873
rs541896944	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72908789	CTCCCATCTCAGCCT[A/C]CTACAGACATATGCC	9873
rs541915920	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72871390	TGTCATTCTCTTTTG[C/T]TTAGCAAGTAAAACA	9873
rs541926175	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72949207	TAATCCCAGCACTTT[A/G]GGAGGCCCATGGCGG	9873
rs541949784	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945274	TCTGATCTTTGACAA[A/C]CCTGACAAAAACAAG	9873
rs541960262	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73060388	GACATTTTGTATAAT[C/T]TCATTTCAAACATTC	9873
rs541963001	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72863429	GGAGAAAATCTTTAT[C/G]ACCTTGGTTTTAGGC	9873
rs541970878	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73045081	TCTCAAAAAAAAAAA[A/G]AAAGAATGGGGTAAA	9873
rs541979431	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72915946	CTGGAGGCCACTATC[C/G]TTAGCAAACTAATGT	9873
rs541981055	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73028102	CACACAGAATGCTCA[C/G]AGGGGCACTGCCTAC	9873
rs541985238	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72984854	GAAACTTATCCCTAA[C/T]GCAGTCTTGAGAAGC	9873
rs542019926	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137886	CAGCTGGGTTGCAGA[A/G]AACCATATATACTAT	9873
rs542025111	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72894188	GCCAATGGCATAACA[A/T]TCTAGTTAACCCTCA	9873
rs542025743	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938076	CCAGGTAGGGAAATA[C/T]ATCCCCAGCACCCTC	9873
rs542034053	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73045662	TCTCAGTAAACTATC[A/G]CAAGAACAAAAAACC	9873
rs542039410	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73094519	CCAGTTGTCCATCAA[C/T]GGGATCATGGATAAA	9873
rs542040866	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120352	AACAATGTACATTTT[A/G]AAAGTCTATTAAGTA	9873
rs542063523	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903308	TGCAAGCTCCGCCTC[C/G]CGGGTTCATGCCATT	9873
rs542073071	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73131419	CTGTAGTCCCACCTA[C/T]TCAGGAGGCTGAGGC	9873
rs542074305	in-del	-/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:72963641	GGTAGGGTGGGGTGG[-/T]TTTGGGATGAAACTG	9873
rs542087817	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010650	CGATTTCTTTGGCTA[G/T]GAACAGTGTCAGTGG	9873
rs542098553	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903971	GGGGGATATATAGAT[A/G]AATAAGACAAACAAA	9873
rs542101962	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73128928	CCAGGCTGGAGTGTA[C/G]TGGTGTGATCTCAGC	9873
rs542105093	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72985977	ATGTGTTGGCAGCTG[C/T]GCCTCATGAAGTAAA	9873
rs542113645	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72930729	GCCTGGGTGACAGGG[C/T]GAGACTCTGTCTCAA	9873
rs542120337	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73091238	TCATGTATAAATCTG[C/T]ATGTAAAGACACGTT	9873
rs542120558	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73056318	ATCTTTAAAATCTCT[C/T]TGATGCAAACAAATT	9873
rs542123212	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73032215	TTTTTATTCTTTATA[A/C]CACTGGATTGTTCAA	9873
rs542124989	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939984	GAACATCTGTGGACT[A/G]CTTGTACAGTCCCCT	9873
rs542125004	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73136166	CTCTTGTCTCTTAAG[A/G]AAAAAAAAAAAAGAA	9873
rs542141853	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977617	TAGTATATGTGCTGC[C/T]GAAGCGAGCACGCTC	9873
rs542153249	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047526	AAAATACTGGTCATT[C/G]ACAGTACCTAGCCAC	9873
rs542159670	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73126255	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	9873
rs542167738	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947200	GTTAAGGGCTTTAAA[C/T]CAAGTGGAAGACCTA	9873
rs542186952	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72961082	CCTAATGCTTTCCAT[C/G]GCCAACATTGTGACT	9873
rs542192116	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73047687	AGAACCCCCTTCTCT[G/T]TTCCTTTCATTTGGC	9873
rs542194969	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123452	CTATGGCTTTTTATA[C/T]ATGCGCAGGCCTCTC	9873
rs542201239	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72923822	CGTCTGCCTGTAATC[C/G]CAGCTACTTGGCAGG	9873
rs542241603	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73095075	TCATTTGAATACAGT[A/G]TAAACAGATGATGCC	9873
rs542250198	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72910893	TATATTCTCATTATT[A/G]ATCCTCTGTCAGATG	9873
rs542255702	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927323	GTGGATACATATCAT[C/T]ATACATTTGTCTAAA	9873
rs542268497	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969062	TTTTCTTTGAAATCA[A/T]TTTAAAATAGTATAC	9873
rs542272239	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72875046	TAACACAACATTTAA[C/T]ATAAACACATATAAG	9873
rs542284297	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72950178	AATCCTTGCCCTTTT[-/A]AAAAAAACTGGGTTA	9873
rs542294380	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72918167	GTATTATTGTAGTTG[A/G]AATTATTTTCTTAAC	9873
rs542300319	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841781	CTTCACTTTTTCCTC[C/T]TACAGATCTCATCAC	9873
rs542301105	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114365	GGGCAGGTCCAGAAA[C/T]GCTGTCCAAGGGCCA	9873
rs542302276	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862859	AAGTCAGTGCAATAC[C/T]GGCATCAAGCTGGAC	9873
rs542303509	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72961090	TTTCCATCGCCAACA[C/T]TGTGACTTTTCACCC	9873
rs542321534	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73070739	CCTAAATGTCAAATT[A/T]AAAAAAAAAAAGAAA	9873
rs542337339	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72975394	GAGAGGTTGGTTAAT[A/G]GGTATAAAATTACAG	9873
rs542343605	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074115	TTCAAAGATAGGTCA[A/G]TTGACTAGAATAAAA	9873
rs542346268	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72854903	AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA	9873
rs542348141	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72901645	CTCACACTTTAACTA[C/T]GGTTAAAAATGGTAA	9873
rs542352851	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72905682	CTATGAGTGAGAACA[A/T]GCAGTGTTTGGTTTT	9873
rs542372671	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72945502	GGGCAAGGACTTCAT[A/G]TCTAAAACACCAAAA	9873
rs542375577	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72912621	TGATTTTGGTATCAG[C/G]GTAATGCTGGCCTTA	9873
rs542391002	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961957	TGTATTTGTTTCATC[G/T]CTGCATCCCTGAAAG	9873
rs542392276	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954039	GAAATGACATAATCT[C/G]ACTTAGGTTATAAAA	9873
rs542403930	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73022705	AATCTCAATCAATAG[C/T]CCAGAAAGATAAAGG	9873
rs542409693	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72962518	AGAACAGGAGTTTAC[A/C]AAATATACTTTATAT	9873
rs542426219	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73058811	GACCTCAGGTGATCC[A/G]CCTGCCTCAGCATCC	9873
rs542440304	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73057799	CCCCACAGCTATACA[C/G]GGAATGAGTTCCCCT	9873
rs542463124	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72906273	CCACTTTTTGATGGC[A/G]TTGTTTTTTTCTTGT	9873
rs542474376	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72957349	TCATCCATGTCCCTA[C/T]AAAGGACATGAACTC	9873
rs542480135	snp	A/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72946548	CTTAAAGTATAATTT[A/T]AAAAAAACTAGACAA	9873
rs542484785	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005416	ACCTATCAGCAACAC[C/T]GACCTAGTTTATCCT	9873
rs542485760	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059719	CTGTGAGGTTTTCTT[C/T]CTTTTTTTTTCTTTT	9873
rs542511208	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950260	CTTTTCAGATATGTA[A/T]TTTGCAAATATTTTC	9873
rs542511976	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72954662	GTAGCAAGTTTGGGA[A/G]GGAAAAATCAAAGGC	9873
rs542516914	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73127563	CTGATACCAACAACA[C/T]AGAATGGCATCTGTG	9873
rs542522066	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72957933	CAAGTTTGGAATTAT[A/G]TAAACATAAATTATT	9873
rs542533275	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73088541	TATAGGCTTCCTTTA[C/T]TTTCTTCTTTTGCTT	9873
rs542539915	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72898790	GATGGAATGCAGTGG[G/T]GTGATCACGGCTCAT	9873
rs542542028	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104120	TCATATAGTTGCTGG[C/T]GGCTAACAGTGTAAT	9873
rs542549052	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051746	AAAACAACAAAAAAA[A/T]TTTGAAATAAATAGT	9873
rs542551570	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840497	CTTTAAGGCCATGAA[A/G]TTAGCTTATTATTTC	9873
rs542557136	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943157	CCACCATGCCCAGCT[A/C]ATTTTTTGTATTTTT	9873
rs542567047	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124273	TGTGGGATGGGGGGA[C/T]GGGGAAGGGATAACA	9873
rs542577977	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72978998	GAGTAGCTGGGACTA[C/T]AAGTGCATGCCTCCA	9873
rs542582427	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73110235	ATATTCCCTCCTCCT[C/T]TATTTTTCAGAATAG	9873
rs542584199	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73047052	TGATAAAAAATACTA[C/T]TAAATATAAAAGACA	9873
rs542586783	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035886	CCACCACACCCAGCT[A/T]ATTTTTGTATTTTTA	9873
rs542590498	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943640	TTGACTTTTGAACAT[A/G]TATGTTTCAGTGTTT	9873
rs542593788	in-del	-/CAG	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73080421	ATTCATATTTACACA[-/CAG]ATACACAGCATAAAT	9873
rs542604257	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73091337	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	9873
rs542609154	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981839	TTAAGAAATTAGCTG[A/G]GTATGGTGGCAGGCA	9873
rs542629670	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73119286	CCAGCCTGCACAACA[A/G]AGCGAGACTCTGCCT	9873
rs542629814	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73073313	TTACTTCTGGAGAAT[C/T]ACAAAGTGAACTTCA	9873
rs542647837	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139313	CAAGGGAAATAAGAA[C/T]TGCAGCCACTCTTGC	9873
rs542662466	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72875370	TATCTATCTAGCTAG[C/T]TATTATTTATTTGAC	9873
rs542665551	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73083070	ATGCGTGATGAAAAA[C/T]TAACCTTTCATAAAC	9873
rs542684931	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72871462	TGTTTCACATATGCA[A/G]GTGGTGATCTCTTCC	9873
rs542693047	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73065577	AAATTGTCTCTGTTT[A/G]CAGATGACATGATTG	9873
rs542704750	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084420	TTTAGAGATAGGGTC[G/T]TGTTCTGTTGCCTAG	9873
rs542705938	in-del	-/TAATT			intron-variant	FCHSD2	GRCh38.p7	11:73008380	TTCATAACCTAAGAA[-/TAATT]TATATAATAACTAGT	9873
rs542707943	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036900	TTCAAAGTTAGTGTT[C/T]CCTACCATCAAAATC	9873
rs542715395	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937166	GAGGACCAAAGGCTT[A/G]ATGAAGGAACTCTTA	9873
rs542715478	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72867269	TGGTACTTAGATCTC[C/T]AACATGAAAAACTAA	9873
rs542729908	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72919133	ATAAAATAAAAAAAA[A/T]CTAAAAAGTGTCAAA	9873
rs542735020	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72964979	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	9873
rs542751474	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858066	CCCCTAACACATGTT[C/T]GGTGCATAGGAGGTA	9873
rs542754998	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982959	TGAAGCCAGGAGTTT[C/G]AGGCCAGCCTGGTCA	9873
rs542763315	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72928892	CCCACCCCACAACAG[G/T]CCCCGATGTGTGATG	9873
rs542771652	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965432	TTACATTCTACCAGG[C/T]GAGACAAAATAAGTC	9873
rs542812943	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858748	AACAAACCTGCAATT[A/G]TATCCCTGAACTTAA	9873
rs542814803	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73094315	TGGAACTCTAACATG[A/C]CATTGGTGGGAATGT	9873
rs542827667	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73075934	GACCAGCCTGGGCAA[C/T]GTGGCAAAACCTCAT	9873
rs542849202	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920644	ATAGAAGGAACAAAG[A/G]TAAGATTTTTTCATA	9873
rs542853495	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73090707	AGACCTTTTACTACA[C/T]TCCTGTTTGTACTAT	9873
rs542862724	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958199	TCAGAGGAAAACCTT[C/T]GGAGCTAAGGACTAG	9873
rs542874383	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72966955	TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGTG	9873
rs542881940	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72851879	TCAGTCAGAGTGGCT[-/TT]TTTTTTTTTTTTTTG	9873
rs542882012	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72868240	ATCCTCAGCAAACTA[A/C]GGCAGGAACAGAAAA	9873
rs542898894	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076836	TTATGCTAGGCCCGG[C/T]GCAGTGCCTCACGCC	9873
rs542927247	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72851458	AAAAATAAAGGTTGC[C/T]GGCCGGGTGAGGTGG	9873
rs542934294	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73043118	GTGAAAGTGGGCATC[C/T]TTGTCTTACTCCACT	9873
rs542940225	snp	A/C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967803	TTAAAAAGAAGTGGG[A/C/G]AGAGAGGCTGGGTGC	9873
rs542947726	snp	A/T	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:73107053	TATATATATATATAT[A/T]TTTAAATGGAGTCTC	9873
rs542957383	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73015668	AAACATTAAAATTTT[G/T]ATAATTTTGAAATTA	9873
rs542960640	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72959378	GGGACTACAGGCGCC[C/T]GCCACCATGCCCGGC	9873
rs542990058	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73060969	AGGAACAAGAACTTA[C/T]ATAGAACTGTTGATA	9873
rs542990882	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946375	CATAGGAAGGGGAAC[A/G]TCACACACCAGGGCC	9873
rs542991125	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939166	ATTCTAAAGTCAATT[C/T]CAGCAAAAACTTGTG	9873
rs542997548	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73010522	TAGTCACTTCTTCCA[A/G]TTTTTTGAATTTGCT	9873
rs543008156	in-del	-/TAAGC	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73059028	TCCCATTTTAGTTTT[-/TAAGC]TAAGCTAAGAAATAC	9873
rs543017989	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890726	ATCATTTTATAGAAA[A/G]GAAAACAGAGGCTCA	9873
rs543024992	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72993933	AAATAAATAAATATC[A/G]GATAGAAAAGCCAGG	9873
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	9873
rs543038619	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73099894	CTCCGAGGGGACTTT[C/T]GGCACTTGCCTCTGC	9873
rs543047095	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73053971	TTTATTGTATTTTAC[-/A]AAAATGTCCATCTAC	9873
rs543057831	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990863	TAACTAAGACCAGAA[C/T]AGAACTGAACGAAAT	9873
rs543060962	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044508	CTTGTGCCCAGGAGT[C/T]TGAGGCTGCAGCGAG	9873
rs543078969	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939902	GGATTACAGGCATGA[A/G]CCACCATGCCTGGCC	9873
rs543096840	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73043943	TTGAATCATCATCCC[C/T]TGGAAGGCCATTCAC	9873
rs543099743	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092839	TAACCCTACCCAAAG[A/G]CAGGTCTTACCTTTG	9873
rs543108864	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087618	GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCGGGA	9873
rs543109739	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087691	GCCTGGGCAACAGAG[C/T]GAGGCTTTGTCTCAA	9873
rs543113931	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940505	AAGCCAAGATGGGTG[A/C]ATACCCGCACATCCA	9873
rs543118927	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72991475	TCAATAAAATACTGG[A/C]AAACCAAATCCAGCA	9873
rs543122281	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73037555	CTCTGGTATAGAATG[A/C]ATTCTTTCTCCATAT	9873
rs543144853	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983571	GATACACTATAAAAA[C/T]ATATTTTTAATAGAA	9873
rs543159156	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73040895	AACTGCTCCCCCCCC[-/T]TCTTTGGTAACTATC	9873
rs543175766	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72884191	TTTCTGCCTAAAACA[C/T]TAACCTGCCTCTAAT	9873
rs543176931	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978659	TGATTGTGACTGAGT[C/T]CTCACGATATCTGAT	9873
rs543212968	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73079425	GGCTGGTCTCGAACT[C/T]CTGATGTCGTGATCC	9873
rs543215946	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969693	TAATTTAATAAGAAA[A/G]CAAATAAAATGGCTT	9873
rs543219061	snp	A/C			intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73140963	ATTAGGAAAGAGAGA[A/C]AGCAGCGGCAGCAGA	9873
rs543220395	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030420	ACTCAATTTACCATA[C/T]ATAAATGTATCCAAG	9873
rs543225958	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72988416	TATAATTCACATATA[G/T]TGAATTCATACAATT	9873
rs543238205	snp	A/G	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:73080316	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	9873
rs543239742	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921388	ACAGCATATAGATAG[C/T]AGGGCTTAATTTGAA	9873
rs543255735	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72979188	AAGCAGTGTGAAAAC[A/G]AACTAATACAACAGG	9873
rs543268216	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880222	AAAACGAATCCATGT[A/G]CAATTGCTATCAAAA	9873
rs543282827	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72985549	AAACTTTCAGGGCTG[C/T]GTGTGAAAGACTCTA	9873
rs543288498	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925258	CTTACCATAATCAGG[A/G]TCATTTCTGATTATA	9873
rs543306817	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72872507	TGTCTATAAAGATTT[A/G]CCTATTCCAGACATT	9873
rs543321527	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72864224	ATGTAAGCAATAAAA[C/G]AACAGGGTGGGCATA	9873
rs543330651	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72973090	TGGGTAAGTTATGGC[A/C]GGGCGCGGTGGCTCA	9873
rs543338214	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971172	ATAAGTAACTGGAAC[A/G]GGTCAAAATATAAAA	9873
rs543344445	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73023109	AACATTTAGAAGAAC[-/A]GAGAAGAAAATCTCC	9873
rs543383159	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856300	GAGAAGTCAGGATAT[A/G]ATGAGTCCAAAAGTA	9873
rs543393033	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111116	TATGCTTGAGAATGA[C/T]CCATGTGCTGAGGAA	9873
rs543398352	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046651	TAAATATAGATAGAC[C/T]TCGCTTACAAGGAAG	9873
rs543401010	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072236	AAACAGAAGGTTTGG[G/T]GAGGAAAATAATGGG	9873
rs543418138	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73001967	TGCTCCTACACTATT[C/T]ATAAACACAATCGAT	9873
rs543421259	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73100234	GACCATTCCTCTTCG[C/T]GTCCCTTCCTCCCTT	9873
rs543424095	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72963832	GGCTCACCTCCTGCT[C/G]TGCGGCCTGGTTCCT	9873
rs543437999	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73002732	TTAATAGCTGTTTGC[C/T]CTTCCAGTCTCAGTT	9873
rs543439310	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73095678	CAAGCATACTTCCTG[A/G]GGTAGTAAACTTAAA	9873
rs543441316	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994398	AGGTAGTAGTAGTAG[C/T]AGCAGCAGCAGCAGT	9873
rs543446783	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886295	CATCTCCTTCTTTCC[C/T]ACCTTCATCTTTTGG	9873
rs543446885	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72895098	AACTTATTCTGACTA[C/T]GCTAGGATAGCAGAA	9873
rs543464099	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064343	AAAGCAGGAAAGATC[C/T]AAAATTGATACCCTA	9873
rs543479941	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73011643	CCCTTCTTGGTGTAG[C/T]GCCATCACACAATCT	9873
rs543498847	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117516	AAATTTCCTTTTGAA[C/T]CATACCCTACAAGTT	9873
rs543499714	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73003213	TTTAACAAAATAATC[A/G]TAAGTAGCACACTTC	9873
rs543508614	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955420	CTCCAGGAGGCTCCC[C/T]GAACCCTGTCCTGGG	9873
rs543534344	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72887056	ACCTTCCATATGGGG[A/G]AGATTTCCTAAGCTC	9873
rs543560585	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73033116	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	9873
rs543560594	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73116931	TATATTTTTTCATGT[A/G]AAACCTTTCCATTTT	9873
rs543560850	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72996014	ATAATAAACATAAAG[G/T]TTATGTAGAAACATG	9873
rs543566870	in-del	-/TCTA			intron-variant	FCHSD2	GRCh38.p7	11:72875348	GTCAATATTATAAAC[-/TCTA]TCTATCTATCTATCT	9873
rs543583427	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73003975	AGCCAGGCGTTGTGG[C/T]TGGCACCTGTAACCC	9873
rs543583728	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124226	GAGAACACCTGGACA[C/G]AGGATGGGGAACATC	9873
rs543596392	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72948372	TTCAAAATTACTGAA[C/T]GTTTCATTTTTCAAC	9873
rs543596845	snp	A/G	6.60469e-05	0.00574622	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72849875	GCCTTCTTCTCTTTC[A/G]GTATCTGCATTAAGC	9873
rs543602079	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72924465	TTTTTTGTATTTTCA[A/G]TAGAGACGGGGTTTC	9873
rs543606453	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73136072	GGCTGAGGCAGAAGG[A/C]TCACCTGAACCCAGG	9873
rs543608961	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841856	CTCTCTAGGGTTCTA[C/T]TGAAAATGTACCAAA	9873
rs543616331	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72949495	AAGAAAAAGAAAAGA[A/G]AAGAAAAGAAAAGAA	9873
rs543620596	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72871915	ATTTTGATTTCCCTC[C/T]GAATTCTCTGCTTGG	9873
rs543621015	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033667	ATACTCAAACTATGG[A/C]ATTCTATACAAATTT	9873
rs543622299	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105430	TACCAGGCTCTTTAT[C/T]TGGTAACATTACTTT	9873
rs543623054	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73025931	ACTGATATGCTCCAC[A/G]TTTTGACTAAAAAAC	9873
rs543624383	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896952	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	9873
rs543629920	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72872126	TCATATACGTCTTTA[C/T]ATAAGACAATTGGAA	9873
rs543644444	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131961	TCTTCTCATTTTTTT[G/T]AATCAGTCACTGACA	9873
rs543673941	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73028484	GAAGTAACTAACTTG[C/G]TTTTGATTTTACAGG	9873
rs543676485	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916036	ACACATGGGAACAAC[A/G]CACACTAGGGCCTAC	9873
rs543684419	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73026870	TCGCTCTCTCTCCTG[A/C/T]GACCATGTAAGACAT	9873
rs543686243	in-del	-/CAAAT	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72980907	GTATGATTAAACCAA[-/CAAAT]CAAATACCCTGCTTT	9873
rs543689279	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72906049	AACTAATTTACACTC[C/T]CACCAACAGTGTAAA	9873
rs543689537	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071539	TACTAAAAATACAAA[A/T]AAAAAAAAAAAATTA	9873
rs543702093	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955907	TTTCCTAGTTCTGCC[A/C]ACTACGGACTCAAAG	9873
rs543702278	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72881245	TTTCTCAAAAGAAGA[A/C]ATAATGGCCAACAGG	9873
rs543703438	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018880	AGTTTTTAAAAATAA[C/T]AGAAGTTTATTCCAT	9873
rs543734023	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989162	AGAAAATGACTTCAT[A/C]CTAAGGACTATACAC	9873
rs543736937	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881925	GGGGGGCGAATCATG[A/G]GGTCAGGAGATTGAG	9873
rs543742186	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72944069	CCAGCATCATCCTGA[C/T]ACCAAAGCCTGGCAG	9873
rs543764470	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73010871	CAGTGAGCTGGGTGG[A/G]TGGGCAGATTCTTGG	9873
rs543775333	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135393	CCTGACTAAAATTCA[A/G]TAATTTTTCCATATT	9873
rs543785302	in-del	-/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73042446	ATCAATACCATGCTG[-/T]TTTGGTTACAATAGC	9873
rs543798939	snp	C/T	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72910065	AGGAGCACCTCTGCC[C/T]GGCCGCCCCATCTGG	9873
rs543803411	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72888432	AATGTAATGGGCTAA[A/T]AAGTAAGTGGGAGGT	9873
rs543810781	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72978453	ACCATCAGAGAAACA[A/T]AAATCAAAACTATAA	9873
rs543848982	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056425	AAATGTAATCTTTTT[A/T]AAAATTATTTTTTGT	9873
rs543851955	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73006393	CAGCAACTCAAACCT[C/T]CTAGTAGTTGGCTCA	9873
rs543856534	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73056115	CTTACTATCTTTGAC[A/C]TACAACCTTGCTTCC	9873
rs543865713	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72864284	TAAAAATATGGACTG[A/G]GTGTGGTGGCTCATG	9873
rs543878691	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958450	TGGAACCCAGGAGGC[A/G]GAGGCTGCAGAGAGC	9873
rs543881033	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72848937	AACGATTTACATTGG[A/G]AAAAAATGCTAACAC	9873
rs543885922	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910530	TAACCTTACCCCCAA[C/G]CCCATGCTCTTTGAA	9873
rs543890545	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860726	GGTGCTGGGAGGCTG[A/G]GGCATAAGAATCACC	9873
rs543893360	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947594	AGCCACACCACTATA[A/T]TGCTGGTCCTAATGG	9873
rs543897983	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142105	GGAAGGCTTGGGGCC[C/T]GGGCGGCCCGGGCGG	9873
rs543899306	in-del	-/T	0.349699	0.22926	intron-variant	FCHSD2	GRCh38.p7	11:73018518	GGTACAGATCTTGTC[-/T]TTTTTTTTTTTTTTT	9873
rs543904018	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104825	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCCTG	9873
rs543908213	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057106	AAAAATAAAATAAAA[G/T]AAATAAATAAAATCC	9873
rs543910309	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016029	AATGATAGGCTGCAC[A/G]TGGTGGCTTACACCT	9873
rs543911195	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907318	TTCCTAATTGAATAC[C/T]CTTTATTTCTTTCTC	9873
rs543951776	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72899938	ATGTCATTAATTTAC[C/T]GTATGACTCTGGACA	9873
rs543959935	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852208	ATGGCTATTATTTAA[A/G]AAGTCAAAAAATAAC	9873
rs543969381	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73011789	CTGACTAATCCCACC[G/T]GAACAGGCTACCTTG	9873
rs543971757	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72949165	ACCACAAAAAGAAAC[C/G]TGGCCGGGCGTGGTG	9873
rs543974920	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72999241	AATTGCTTAGATGTA[A/G]CATAGATCATCAGCA	9873
rs543980503	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108129	TGGGGTAATATCTCA[C/T]TGTAGTTTTGATATG	9873
rs543999183	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897608	CAACTGTTGTCATTT[C/T]ACACATGAGGAAGCT	9873
rs544007335	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988384	TTCTTTTCCTACTTA[C/T]TCTTAAAAAAAGGTC	9873
rs544008847	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052604	AACACTGTCGAAAAT[A/C]AACAATGAAACAAAT	9873
rs544010720	snp	A/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72941384	TAAAAACTATACTTA[A/T]ATTATAATTTATATA	9873
rs544025794	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844786	TTACACAAACAAAAA[C/T]AAGGCAAAAAAGGGG	9873
rs544037279	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999824	AAGTTATACTAGTAT[A/T]AATTCTCTGCCCCTA	9873
rs544048651	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100101	ACAGTGGCTGTGACA[A/C]CCCGCTAATCCTCAC	9873
rs544057484	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73037824	CACTTGTTATGCATA[C/G]AGCAGAACCTCAAAC	9873
rs544058634	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73089401	GGTTAAACACATCAT[G/T]AGCATATGATCCAAC	9873
rs544060193	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933915	GGAGTTCAAGACTAA[C/T]TTGGGCAACACAGCA	9873
rs544069295	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73044708	GCTGGGTAAATACTA[C/T]ATAGAAAACAGTGCA	9873
rs544091900	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72884391	GTGATTAGTCAAGAG[G/T]TCTGCTAACATAGCA	9873
rs544093765	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893189	TATTTTTAGTAGAGA[C/T]GGGGGTTTTGCTATG	9873
rs544094637	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942061	CTCAAAATCTCATGT[C/T]GAAATGTGATCTCCA	9873
rs544097569	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846230	GTGTTGCCCAGGCTG[A/G]AGTGCAGTGGTGCCA	9873
rs544102705	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72907793	AGAGACAGGGTTTCA[C/T]CATGTTAGCCAGGAT	9873
rs544117461	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038533	TGAAAAGAATGAAAT[C/T]TTGTCCTTTGTAGCA	9873
rs544119502	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119076	GGAGGCCAAGGCAGA[C/T]GGATAGCTCAAGCTT	9873
rs544129558	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885393	ATACTTGCATTAGAA[A/G]AGGTGAGACATCGTG	9873
rs544157594	in-del	-/ATG	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72884563	ATATAGTTTATATAT[-/ATG]ATGATATATATAAAA	9873
rs544166742	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73122177	GCTAACTTAAAAGGC[-/A]AAAAAAAAAAAATGT	9873
rs544178976	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023268	ACAAGCTGCAGATTA[A/G]GAAAAAATACTTGCA	9873
rs544180312	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913432	TGCCACCACACTTGG[A/G]TAATTTTTGTATTTT	9873
rs544180482	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031407	CTTGAGGGCGGGAGG[C/T]GGAGGCTGCATTGAG	9873
rs544182850	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73118472	GTTCTGCCTGTTTTA[C/G]AACTTTTCAGTATAT	9873
rs544184510	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72864192	GTGATGTTAACATTG[C/T]GGGCTATAGTTTGAA	9873
rs544199323	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034012	TAGACAATTTTAATA[A/C]CGATAGCAAATATAT	9873
rs544209367	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877205	TCAGTTTTTTTAATG[A/G]TTAGTGTTTGTTCTC	9873
rs544228025	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72875072	ATAAGTGTAAAGCTA[C/T]AGTTGAATTTCAAGT	9873
rs544236164	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73059912	ACCAAAACTTTGCTT[A/G]TATCTGCAGAAATTC	9873
rs544236272	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067629	GACCTGGTTCTACAT[C/T]AAAGACTTAGGAGCT	9873
rs544263128	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126604	AACTAATACGAACTT[C/T]TATAATATCTGTTAA	9873
rs544271643	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72908039	ATCTGACTACCCTTC[C/T]CAGACTCTGGTAAAC	9873
rs544276031	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951098	GCTATCTGAGTCTCT[A/G]AATAACTTCATGAGG	9873
rs544279752	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72931520	GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAG	9873
rs544320838	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024190	TACCAGTGGTTGGGG[A/G]AACCGAAGATAGAAT	9873
rs544321051	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72931126	TTTGAAAAGGAGTCG[C/T]GCTGTGTCACCTAGG	9873
rs544332923	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878675	CTGGAATTGATAATA[C/T]ACTAAATAGATAAAA	9873
rs544333499	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72925540	TTAAAACAAACAAAC[A/C]AACAAATAAATTTCT	9873
rs544340785	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852919	CTGCATGTTCTCACT[A/C]ATAAGTGGGAGCTAA	9873
rs544340863	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72969372	CTGTGCAGAAAAGCT[A/C]GTTGGCATTTAGGTT	9873
rs544342448	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72889494	ACACATATAATGCTT[A/G]AGCAAAGGAGTTTGA	9873
rs544355849	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72845387	AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGC	9873
rs544359133	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72855476	GTGAGACTCCATCTC[-/A]AAAAAAAAAGAGTTC	9873
rs544362242	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72900548	AAATTAGTCATAATT[A/T]TAAGACAAGCTTGAC	9873
rs544362933	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951776	TTTTCCCATTGATTT[A/G]AGGTTTACCCTTTCA	9873
rs544365801	snp	A/C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73068735	AACACTTTGGGAGGC[A/C/T]GAGGCAAGAGGACTG	9873
rs544389608	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870468	ACCAATTCTTTCAAG[A/T]TTGGCTCTACCAATC	9873
rs544389994	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73053389	GACTACTAATGAAAG[A/G]TAGAAAATGAATTCT	9873
rs544396200	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72944502	CACAAGACAGGGATG[A/C]CCTCTCTCACCACTC	9873
rs544402062	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73098361	GCATATTTTCTGTCC[C/G]CTTCTATTAATTGAT	9873
rs544411012	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062039	CCCAGTAGGGGCCAA[C/T]AGACACCTCATACAG	9873
rs544413122	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006657	TACAGCAATTGCTGC[A/G]CAATCACTTCTTGGC	9873
rs544439461	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908894	CCTGGGCTCAAGCGA[G/T]CTGCCCACCTTGGCC	9873
rs544449320	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73133065	TCAAAGCCACTTACA[A/G]TATCACTTCACATCC	9873
rs544450501	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093088	CTAAGTGACTGAACC[A/G]CAATAAAAACTGCAT	9873
rs544451849	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73045048	GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC	9873
rs544455898	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73077052	GAGGCGGAGCTTACA[A/G]TGAGACAAGATTATG	9873
rs544483195	snp	C/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72945121	AAAAGAACAAAGCTG[C/G]AGGCATCACACTACC	9873
rs544486926	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046141	GACTAAAGACACACA[C/T]CATGATGCCATGCTG	9873
rs544488155	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72966907	AACCCTGATTATGAG[G/T]TAAGAAAGTGGCCGG	9873
rs544491019	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72891083	ACCATACTCAGCTCA[-/T]TTTTTTTTTTTCCTT	9873
rs544492827	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72992367	GATTCAATGCCATCC[C/T]CATCAAGCTACCAAT	9873
rs544497767	in-del	-/TA	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72866905	GGGAAGTTGGGAGGT[-/TA]TAGAGTTTTAGCTTT	9873
rs544498822	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108862	AGGCGTGAGCCACCG[C/T]GCCCAGCCTAGATTT	9873
rs544499820	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72980616	AGTCCTCCAGCAGTA[A/C]GTGATTTCCATCACT	9873
rs544513637	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093631	TTTGAGACCGAGTTT[C/G]GCTCTTGTTGCCCAG	9873
rs544523212	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109440	CAGAGATCTTTCACT[A/T]CATCAGTTAATTCAT	9873
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	9873
rs544555948	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909478	TAGGAAGTGAGGAGC[A/G]TCTCTGCCTGGCCGC	9873
rs544560374	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72984676	TCAGGCATTCCACAG[C/T]GTGAAGTTTCCGAAG	9873
rs544582730	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930622	TGGTGGTGCCCATCC[A/G]TAGTCCCAATTATTT	9873
rs544586336	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73102291	GAATGCTAAATAATA[C/T]AGATAGACTCTGGGG	9873
rs544588514	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010182	GCTTGATCTAGTCTA[C/T]TGTTGAAGCTTTCAA	9873
rs544593149	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73069343	AAAAAGACTACAAAA[G/T]AACTATCCAAAGAGA	9873
rs544609862	in-del	-/TGTATAATATACTGAA	0.0341408	0.126114	intron-variant	FCHSD2	GRCh38.p7	11:72907439	AATGCTTCCAGTTTT[-/TGTATAATATACTGAA]TGCCCATTCAGTATA	9873
rs544620004	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72976492	ACTATGCTGCCCAGG[C/T]TGGTCTCAAACGCTT	9873
rs544636773	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72923349	GGTCATATGATAACT[C/T]TATGTTTAATTTTGA	9873
rs544638146	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125668	CATGACCGCACCACT[A/G]TAACCTAGCCCAGAC	9873
rs544658265	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73100322	GGCACTGACCTAAGC[A/G]CTTTACATGCTTTTG	9873
rs544661598	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035179	ATGTATGTATGTATG[C/T]ATGTATGTATGTATG	9873
rs544674781	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73077966	AGTAAGAGTGAGGGC[A/G]GTAATGGCAGGGAAC	9873
rs544676383	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72933742	GCTTAAAGTAGACAA[C/T]TTTTATGTCAAAGCT	9873
rs544701489	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73133916	AGGGTTATGGGGAGC[A/G]ACTGCTAATGGGTAC	9873
rs544706234	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967947	ATACAAAAAATTAGC[C/T]GGGTATGGTGGCGGG	9873
rs544713892	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024955	GATACTATCTAACAC[A/C]AGTCCAAATGGCTAT	9873
rs544718837	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927180	TCAGATACGAGCTGC[C/T]TTCCATTTTCTAAGG	9873
rs544726479	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862016	AATATCTGAATAATC[A/G]TCAATGCAATTACAC	9873
rs544748739	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72968824	CCCAAGGTTCATCCT[C/T]TGACCAACACTTCTC	9873
rs544753757	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72917405	TGACCATAGATGTTC[A/G]GGTTTATTTCTGAAC	9873
rs544760096	in-del	-/TTTTTTTTTTTTTTTTT			intron-variant	FCHSD2	GRCh38.p7	11:72916986	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTT]GAAGCAGAGTGTTGC	9873
rs544786891	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854338	ATGTCCATTGAGAGA[G/T]GAATGGATAAGTAAA	9873
rs544787011	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141391	AAGCAGGCCAAACCC[C/T]AAGGCTAGGCTAGAA	9873
rs544801818	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73111654	TATTTTTGGGTGTGT[A/G]GTCATCTCTTCCTTC	9873
rs544824453	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72898805	TGTGATCACGGCTCA[C/T]TGCAACCTCCACCTC	9873
rs544826330	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111603	AATCCATTTACATTC[A/C]ATGTTGTTACTGATA	9873
rs544829734	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909193	AGGCACACGCCGCCA[C/T]GCCTGACTGGTTTTT	9873
rs544852572	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140612	AATTACTCCATAATG[A/G]CTGCGAAAAAGCACA	9873
rs544855637	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118373	TATCATCCCAAAAAG[A/T]TTCCTCATGCCCCAT	9873
rs544863380	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73020496	AGTGATCTTTTAACA[A/T]TGAACAAGTTCACTG	9873
rs544872267	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73058037	GGCGCCCACGACCAC[A/G]CCTGGCTAATTTTTT	9873
rs544882465	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066095	CATCACGCTACCTGA[C/G]TTCAAACTAGGGCTA	9873
rs544913461	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72911721	AGGGTACATGTGCAC[A/T]ATGTGCAGGTTAGTT	9873
rs544916755	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125588	CACACATCTGTAGTC[C/T]GAGCTACTCAGGAGG	9873
rs544916792	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73117820	CCATTAATTAATCCA[A/C]CTTATTTTTGGTGTC	9873
rs544918826	in-del	-/ATGTAGTGTAC			intron-variant	FCHSD2	GRCh38.p7	11:73081736	ATTTTATAAATATAT[-/ATGTAGTGTAC]ATGTATGAAAGTGTA	9873
rs544929183	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110188	GGTCTTTGGTATCAG[C/G]GTACTGCTGGCCTCA	9873
rs544941248	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949373	GAGAATCACTTGAAC[C/T]CTGGAGGCAGAGGTT	9873
rs544950236	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905710	TTTCTGTCCTTGTGA[C/T]AGTTTGCTTAGAATA	9873
rs544968267	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855415	CGGGAGGCGGAGGTT[A/G]CAGTGAGCCAAGATC	9873
rs544972325	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72873329	TGAGACTCTGTTTCA[-/A]AAAAAAAAAAAAAAT	9873
rs544978013	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72942316	AGGCCTCACCAGAAG[C/G]AGATGCCAGCAGCAT	9873
rs544980557	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72870527	GTTATAAACTACTGT[C/G]TCTCTTTAATAATAA	9873
rs544982271	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73089263	ATGATATTAATGGAT[A/G]CTATAATAAAACAGA	9873
rs544987923	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949804	GGGTTGTTTCCACCT[C/T]TGGATTGTTATGAAT	9873
rs545022936	in-del	-/C	0.000816493	0.0201886	intron-variant	FCHSD2	GRCh38.p7	11:73097634	TTTTTTTTTTTTTTT[-/C]TAATTACTGATTCAA	9873
rs545044023	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73067910	AAAAGAGGATTAATG[A/G]ACTGATAGTTCCATG	9873
rs545046140	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027696	CATTTCAGAGATGTT[C/T]GCTGCACTCCCCGCC	9873
rs545072411	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72903471	TGATCCACCGGCCTC[A/G]GCCTCCTAAAGTGCT	9873
rs545074194	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72873654	TAAGAAACTAATCCA[A/C]GGCCACAAAGACTTA	9873
rs545097204	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099265	CCACTAGGATGGCTG[G/T]AAAACAACACAAAAC	9873
rs545097529	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091522	CCACTGCACTCCAGC[C/T]TGGGCCACAGAGTGA	9873
rs545106599	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72997770	CAGTGGCACGATCTC[A/G]ACTTCCTGCAATCTC	9873
rs545116211	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971392	AGTGTCAGTAGAACA[C/T]AATCACTCTTGTGAT	9873
rs545117588	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72964089	ATGGATGATACAAAC[A/C]TGGATAATATAGTTA	9873
rs545138076	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910778	TATTATCCTATGACC[C/T]TGCCACATCCCCCTC	9873
rs545141367	snp	G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73043033	CTCTTTTCCTATTTA[G/T]ATGCCTTGAATTTCT	9873
rs545160649	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092076	TATGATCTCATCTGA[A/G]AAGCCTTCCTGAATT	9873
rs545162435	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857238	AGAATAATTTCTTCC[C/T]TTTTCCTCTTCCACT	9873
rs545173776	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73040235	TTATGCAAATGCCAA[C/T]CAACCCAGCTCTTTT	9873
rs545190229	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73069724	GATACAAATAATGTT[A/G]AAGAAGCAATATTTA	9873
rs545198293	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72866148	CAAGTGGGCCTGGAA[C/T]TTGCTGTCATCAAAA	9873
rs545205614	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72972160	TCTGCTTCAGTACCC[C/T]TCATCTATTGTTGAT	9873
rs545237433	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73107152	TTGATTCTCAAGACT[C/G]TCCGCAATTCTTGAG	9873
rs545239664	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73139565	ATAAACACACTTCTC[A/G]CTAAATTTGGCACTC	9873
rs545267298	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72969628	ACATTAAAAGACTAG[A/G]AAAAAGCCCAAATGT	9873
rs545271827	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73012963	TCAAATATGAGATGA[C/T]GAGGAATTAAATTCC	9873
rs545276787	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73099882	GCCTCTCGGTCACTC[C/T]GAGGGGACTTTCGGC	9873
rs545282278	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72932270	TATTGCAGCAATCTT[C/T]TGTTGCCCTGCATCC	9873
rs545288450	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72875434	GTGGTGCAATAATAG[C/T]TCACTGTAACCTTGG	9873
rs545289682	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974175	CGTTTATTTGGTTCA[C/T]GGTTCTCGGGACTGG	9873
rs545296770	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084221	ACAATGTGAAAATCA[A/G]ATTTTGATTGGCTTC	9873
rs545297143	snp	A/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73105619	TCTGAAGATTAAGTA[A/T]AATAAATGGATATAA	9873
rs545310469	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857919	TGGGTTTGAATGTTG[A/G]CTATGTCACTTACTT	9873
rs545310548	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73035678	TTTTAAGTACTGAAC[A/G]GTACTGAAATGTTCA	9873
rs545329404	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73013688	TGAGTTCTTAGCACA[A/G]TGTCTGCCACATAGT	9873
rs545333321	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73004338	GGAAATAGCACCTCC[A/G]TGGTCATAACCTAGA	9873
rs545354934	snp	C/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72906183	TCTCTGATGACCAGT[C/G]ATGATGAGCATTTTT	9873
rs545390126	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72897891	TTCAGCAAAAAAGAT[G/T]TATTTTACTTTTTCT	9873
rs545392085	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005318	ACTTTAGTGTCTACC[A/G]CTCTTCTGAAATTGC	9873
rs545407997	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72966217	CAGGAAGGAGTGCAG[A/T]GGTGCGATGTCGGCT	9873
rs545425143	snp	A/C	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72889465	CTGCTGAGTGTTGAG[A/C]AAGTACAGAAAAAAC	9873
rs545440808	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072355	ATGTCCCCAAGAGTA[C/G]TAACATTTAATTATA	9873
rs545451536	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73000236	TAAAATATTATTTCC[C/G]GAAATAATTACTTTA	9873
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	9873
rs545507178	snp	C/T	2.35691e-05	0.00343278	intron-variant	FCHSD2	GRCh38.p7	11:72889991	TATTGCTATCCTTAT[C/T]GTAACCACTACTGCT	9873
rs545517758	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043744	TTAAGAGATATGATA[C/T]GTGTTACATTCAGTT	9873
rs545537336	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839475	AGACTTTTGTAATCC[C/T]CTGAATGAGAGTTGA	9873
rs545539659	in-del	-/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140827	CTCGCCCGCCAGGCC[-/G]GGGGCCCCAGGGTTC	9873
rs545546372	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083448	CAGCTACTCAGGAGG[C/G]TGACACAGGAGAATC	9873
rs545550408	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035963	TGACCTTGTGATCCG[C/T]CTACCTCAGCCTCCC	9873
rs545550551	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990754	GCCCACAAGAGAAAG[A/C]AGGAAAGATCTAAAA	9873
rs545581545	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936533	TACTCCCAGCACTTT[G/T]GAAGGCCAAGATGGG	9873
rs545600639	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986504	GTGAGCCACCGTGCC[C/T]GGCCCCAATTATTTT	9873
rs545614494	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046424	GAATATGTCTGAATA[C/T]CAATTTTCATAGAAA	9873
rs545634626	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72876235	TTCGGGAGGCTGAGG[C/T]GGGAGGATTGCTTGA	9873
rs545644187	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72919361	GGAGTGAGATACTCA[C/T]ATGAGTGAATGCAGA	9873
rs545676699	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029421	GATTTGGAGAGTAAA[C/T]TACAGTTAATTTAGG	9873
rs545677053	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73092827	ACAGTAAAGGATTAA[A/C]CCTACCCAAAGACAG	9873
rs545685562	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72866541	TCCCAAAGTGCTGGG[A/G]TTACAGGTGTGAATC	9873
rs545703127	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72999815	CTGGTTGGGAAGTTA[C/T]ACTAGTATTAATTCT	9873
rs545748808	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73120583	AAAAATACAAAATTA[A/G]CCGGGCGTGGTGGTG	9873
rs545760547	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73067015	TTATAAATCATTCTA[A/C]TATAAAGACACATGC	9873
rs545765176	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130164	CAGGTGTGAGCCACC[A/G]CGCCTGGCCCATAAT	9873
rs545768586	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73021458	AAACTAATGCAAGAA[C/G]AGAAAACTAAATAAT	9873
rs545774371	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017744	CATTGCATGAAAATA[C/T]CTTCTAACCACTCCT	9873
rs545774448	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73091837	TTGAGGTCAGAAGTT[C/T]GTGACTAGCCTGGCC	9873
rs545778144	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879403	AAAAACTTAGTAGGT[A/C]TTTGAAAAGCAGAAA	9873
rs545779382	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901478	TACAGACAGAAAGTA[G/T]ATTAATGATGTCAGG	9873
rs545784873	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73130961	AATTCTCCCTCTCAA[G/T]ATTTACAACATTTTA	9873
rs545787717	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054448	GATGGGCATGTAAAC[C/T]CTTCAATGTAGTCTC	9873
rs545817371	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893333	ACATTTTTCTTTTTG[A/G]AAGACAGGTTCTCAC	9873
rs545819752	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863530	AATTAAAAATTTGTG[A/C]TCTTTGAAAGGTATT	9873
rs545825638	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72963899	GTTGGGGACCCTGGA[A/T]TAGATGACAACTCTG	9873
rs545829110	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72924184	GGGTTCCAGTAATCC[A/G]CCTGTCTCAGCCTCC	9873
rs545833265	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080248	ATTACACTAAGCTAT[A/G]ATTGTGCCACTGCAA	9873
rs545868115	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73113610	TTGTGGATATTTGTC[A/G]GTGTCCAGGCATTGA	9873
rs545881438	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864178	CTGAAAACGGGGAAG[C/T]GATGTTAACATTGTG	9873
rs545886724	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73045761	CATCACACTCTGGGG[A/C]CTGTTGTGGGGTGGG	9873
rs545888765	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959513	GTGCTGGGATAACAG[C/G]CGTGAGCCACCACGC	9873
rs545894055	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939010	CTACTAAACATGTAA[C/T]GCAGGATATTTTCAA	9873
rs545898853	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970357	TCTAATGTATGAAAA[C/T]TGTCTTTTATCTAAA	9873
rs545899648	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010709	TGCAGTTATTAGTGG[A/G]GCCTGTGGTAAAGTT	9873
rs545914739	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033414	GGACAAGTTTTAGTG[C/T]AAAGAATTTTAGAAT	9873
rs545932522	snp	C/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73002900	TTAACATCTGTCCCT[C/G]TCACTATAGTGAAAG	9873
rs545935555	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962828	AGCAATTAGAGTCAA[C/T]AGATTACAGAACTGC	9873
rs545954415	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72994126	ACCAAACAGAATAAC[C/T]GGTCAGCTATGTGGA	9873
rs545959286	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002652	AGAAAGAGAGGAAGG[C/G]AGATACCCTTCATCC	9873
rs545962088	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72909996	CACCTCTGCCCGGCC[A/G]CCCCATCTAGGAAGT	9873
rs545982504	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856103	GCCTTCATAGGAGAG[A/C]CATTACATTAATTAA	9873
rs545993573	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72878878	TTGGGAGGCCGAGGC[A/G]GGCAGATCACTTGAG	9873
rs545997545	snp	A/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72922262	GGTGTAGGAGTTAAG[A/T]GAAATAATAAACGTG	9873
rs546015473	snp	A/C/G			intron-variant	FCHSD2	GRCh38.p7	11:73100476	TCAAGCGATTCTCCC[A/C/G]CCTCAGCCTCCCAAG	9873
rs546017847	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72931626	AAAAATTAGCCGGGC[A/G]CAGTGGCAGGCATCT	9873
rs546018019	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040151	CTGAGTTCATTTGTT[C/T]TGGACAGGTGGCCAG	9873
rs546018892	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73003095	AAAAGAGACCTTTAG[A/G]GTTTAGCAGATTTAT	9873
rs546025217	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954276	AGTGGCACAGCATGG[C/T]GGCTCACTGCAAGCC	9873
rs546034005	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72953844	TGGCATTAAGAGCTT[A/G]CTTGAGGAAACATCA	9873
rs546045887	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848808	TCTGGGACGTTCAAG[C/T]AAATATAATGGGAGG	9873
rs546048421	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143945	CACCAGAATCCTTAA[G/T]CAAATCAGGGAAGGC	9873
rs546052592	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73137363	CTTGGAGCACCAACA[A/G]TCTCTGTCTTTACAT	9873
rs546054576	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932389	ACTGGCTACTCATCA[A/C]ATTTAGGAAAAGGCT	9873
rs546057521	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041016	TTATTTCGCTTAACA[C/T]AATGACCTCCAGTTC	9873
rs546062898	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73098473	TCTAACATATGATCT[A/G]TCCTGGAAAATGTTT	9873
rs546065257	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72928257	AAAAAAATTCCACAA[A/T]ATTTTTTTCAATGGC	9873
rs546077162	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73031471	ACAAGACCCTGTCTC[C/T]GAAAAAAAAAGAGAG	9873
rs546077998	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72896889	TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG	9873
rs546080755	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73033010	AGTACTTAGATTGGC[C/T]GGGTGCGGTGGCTCA	9873
rs546085146	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057038	CAGTGAGCCGAGATC[A/G]CACCACTGCACTCTA	9873
rs546117842	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104773	GGGGTTTCACCACCA[A/G]GCCAGGCTGGTCTCA	9873
rs546122866	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041710	TCTCTTCACTATGTT[A/G]ACTGTTTCTTTGATG	9873
rs546124094	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73135368	AAATGAACAAACATG[A/G]TAATATCCACCTGAC	9873
rs546136533	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73060798	CTAGGTTAAGAAGAA[C/G]GCAATGGAGAGTTTG	9873
rs546143883	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72905422	CCTTACTTTGTATTA[C/T]AAAAAATCCAATTAT	9873
rs546175105	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995673	CATGCCACTGCACTC[C/T]AGCAGGGGTGACAGA	9873
rs546178343	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848710	TGGGATATGCCAACA[A/G]AGGGAATGTTGAATG	9873
rs546181131	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142528	GGCACGGGGCTTCGT[A/T]CCGCGGCAGGGGAAG	9873
rs546207620	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73127358	CTAACAAAATGAAAT[G/T]AACAAAAATACCAGC	9873
rs546221975	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909673	TGGGAAGTGGGGAGC[A/G]CCTCTGCCTGGCCGC	9873
rs546241357	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72883095	GGAACAACTGGCTAT[C/T]TGTATAGGAAAAAAC	9873
rs546260203	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916449	TCCCGAGTAGTTGGG[A/G]CAACAGGTATGCAGC	9873
rs546272149	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120253	TTACATCCTTGTATA[C/T]TTATTGAACTATGGA	9873
rs546280300	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72954102	ATAAAGGTAGGGGTG[G/T]GAGTAGAAAGCCAAT	9873
rs546281242	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72848320	CATTTCCTGAACACC[C/T]CACACTCTCATCACA	9873
rs546282962	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72852847	TTCTGTAGGAACATG[G/T]ATGGAACTGGAGCCC	9873
rs546289491	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110973	TTCCATGTGGTTATA[G/T]AGTTTCCAAAATTAT	9873
rs546290042	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73127002	GAGATTGCACCACTG[C/T]GCTCCAGCCTGGGAT	9873
rs546300665	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73063449	AACAATATTAACCTT[A/C]AATGTAAATGGGCTA	9873
rs546317190	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962065	ATCTTCAATTTTAGT[A/C]TTAGAGTTTCTTCTA	9873
rs546322049	in-del	-/AAAC	0.088267	0.190637	intron-variant	FCHSD2	GRCh38.p7	11:72868694	GACTCTGTTAAAAAC[-/AAAC]AAACAAACAAACAAA	9873
rs546323657	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004727	TGTGGCTGGAGAAAA[A/G]GATAATTACGTTGCC	9873
rs546326626	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911580	CTGCTTTGGGTAGTA[C/T]TGACATTTTAAGAAT	9873
rs546335273	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042668	GGTCATGTTAACAAT[A/G]TTCATTCTTCCAGTC	9873
rs546340346	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72949448	AAGAGCAAAACTCCA[C/T]CTCAAAGAAAGAAAG	9873
rs546346166	in-del	-/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72887684	GACTAGTAGCCATAA[-/T]TTTTTTTCATTTATT	9873
rs546350851	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104243	TTTACTTTGCTTCTC[C/T]TAAACAGAAAAGATG	9873
rs546355293	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73074250	TAGAAAAATAAACTT[C/T]TCTATATGGATTTTC	9873
rs546375758	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935300	AGTAAGAACTTTAAA[C/T]AGTCCCCTCCTTATT	9873
rs546390177	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73098541	GGGTGGAGTGTTCTA[C/T]ATACACCTGTTGGGT	9873
rs546391236	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73132283	TTTCCACTAATAACA[A/G]TAGCTACCAATGCTA	9873
rs546392775	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73015103	CCTGCCTTGGCCTCC[C/G]CAAGTGCTGGGATTA	9873
rs546398465	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043236	TGTTCTTTCTATGCC[A/C]AGTCTGTTGAGAGAT	9873
rs546404971	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947492	TCACATAGGAATTGA[A/C]CACAAGATCTTATTC	9873
rs546410257	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72995090	TAATATGTGGCCTTA[C/T]GTTTCTCACTTCTTT	9873
rs546425945	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72942625	TTTCTGTACTTTTCA[A/C]ATTTTCTTCTGGTAC	9873
rs546442634	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72889543	GGCAAGACCCTATCT[C/T]TACAAAAAATCTAAA	9873
rs546451244	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940682	AAGGTTACATTATAT[A/G]TAGGATTCATGTTCA	9873
rs546456313	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096522	TGCTGCTGCACTCCA[G/T]CCTGGGTGGCAGAGC	9873
rs546456548	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72999176	AGGTTTCTTTCATTT[A/G]CTATCTCAGAGTCCT	9873
rs546459933	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036245	TACAATTAGAAACAT[C/T]AAAGTATTGGAGCCA	9873
rs546462501	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126858	GCCTGACCAACATGG[A/C]AAAACCCTATCTTTA	9873
rs546479001	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882216	GGGAGGCCAAGGCGG[A/G]TGGATCATGAGGTCA	9873
rs546487702	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933285	GCCTATCCTTCCCAC[A/C]AAAGTTATTCTTCCT	9873
rs546493264	in-del	-/A	0.0193772	0.0965046	intron-variant	FCHSD2	GRCh38.p7	11:72901690	GTATTCTGCTACCAT[-/A]AAAAAAATGGCAGAG	9873
rs546496104	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73058005	CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGACTAC	9873
rs546496996	snp	C/T	3.6632e-05	0.00427957	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841000	ATTTTACTTGAGTTG[C/T]TGAGCAATAATGCTG	9873
rs546499177	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987710	TCCACTGTGCTCATG[C/T]TCATCCTGTGGGCTG	9873
rs546513744	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73091673	AGGCTCATGCTTTCA[C/T]GTTCTAGCAAATGTG	9873
rs546515511	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72851557	CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC	9873
rs546517331	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096941	TACTGAGATAATCAT[A/G]TGGTTCTGTCCTTCC	9873
rs546525271	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036942	TTCATCTGTTAACGC[A/G]GATCTGTAATTAGAT	9873
rs546528777	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72912011	ATTTTGTATCCTGCA[A/G]CTTTACTAAAGGTGT	9873
rs546538806	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73099073	AAAAATTAATTAGTC[A/G]GAGGTAGTGGTACAT	9873
rs546547862	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074842	ACTTGAGCTCAGGAG[G/T]TCGAGGCTGTAGTGA	9873
rs546605506	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062923	CCAATATTCAAATTC[A/C]GGAAATACATAGAAC	9873
rs546610095	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73029120	GTAGTACACTAAAAA[C/T]GATAAAATGCCATTG	9873
rs546617260	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73075308	CATTCCTTAGGTAAA[C/T]ACCCAATAGAACACA	9873
rs546619086	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920758	ACATACTACATAGAT[A/T]CCTCAATTAATGTTT	9873
rs546624649	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73135311	CTTCAACAATATAAT[A/T]CACTTCATTTCACTG	9873
rs546629435	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73058393	GACATGGTATGGCTA[G/T]ATGTCATCACAATTT	9873
rs546642365	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72956765	CTCAACATATGAATT[C/T]TGGGGAAACTTCAGA	9873
rs546642390	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73107706	CGTGCAAATTTATCT[C/T]TTCTGTGTCTGGCTT	9873
rs546664284	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883804	AGGCATGGTGGAGTG[C/T]GCCTGTATTCCCAGC	9873
rs546667366	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72919654	TTAGCTATCTGTTAC[A/G]ACTATAATGTTTCCT	9873
rs546668634	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73096609	TTCCAGATAGAATTA[C/T]AGAATGTCAAACACA	9873
rs546680568	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067240	ATCACAACAGAAAAC[A/G]AAACACTGCATGTTC	9873
rs546690559	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73056145	CCTAAGTGTCTTACT[C/T]ATCTGGACCAGCAGA	9873
rs546690774	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73092174	GCTCCATCACTAAGG[C/G]TGGAGTACATTGGTG	9873
rs546704088	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72913118	CTCACTCACTACCAA[C/G]AGAACAGCAAGGGGG	9873
rs546723654	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72958847	ACAAAATTCAGACTC[C/T]TGTTTCATAAAAGGA	9873
rs546730125	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098469	ATAATCTAACATATG[A/C]TCTATCCTGGAAAAT	9873
rs546743019	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72997902	GACGGGATTTCACCA[C/T]GTTGGCCAGGCTGAT	9873
rs546745223	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067855	GTCCATTTTCACACT[A/G]CTGATAAAGACATAC	9873
rs546758851	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943246	GATCTGCCCACCTCT[A/G]CCTCCCAAAGTGCTG	9873
rs546766351	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950455	CCTCAAAGAGTTTTA[C/T]ATAGTTTTAGCTCTT	9873
rs546777640	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72859373	TCTCGGTTATCCCAA[C/T]TGACTGTCACCATAT	9873
rs546790116	snp	A/C	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73118673	CTTCATTACTGATTT[A/C]TATTTTCATTGCATG	9873
rs546790890	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098871	TGCATTCCTAGATGG[C/G]AAACCAAAAGCACAA	9873
rs546810885	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72959473	ATCTCCTGACCTCAT[A/G]ATCCGCCCGCCTCGG	9873
rs546818710	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72942289	CCTTCTGCCATGATT[A/G]TAAGTTTCCTGAGGC	9873
rs546860339	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990325	CCTGGTAGGCAAACT[A/G]CATCAATTTGGGATA	9873
rs546866893	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141739	CAAGTCGGTGACAAG[A/C]CCAAGACGAGGGCGG	9873
rs546875266	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092268	AAGTAGCTGGGACTA[C/T]AGGTGTACACCACCA	9873
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	9873
rs546896239	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052159	GTGATCTGAACATGA[A/T]GGTGCTGTGAAGGAA	9873
rs546897172	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982186	AAAACGTTTTTGCAA[C/T]AGGATACTTCTTAGT	9873
rs546898764	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100275	CCCTTCTCCTATTAA[C/T]AACAACAATTAACAG	9873
rs546920649	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908296	GTTGATGGACACTTA[A/G]GTTGCTTCTAAATCT	9873
rs546939221	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72943962	AACTTTAACTTCTAT[C/T]GCATGACATGGAGGT	9873
rs546955215	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891294	TAGAAATTGATAAAC[C/T]GGATTTTAAAAATTA	9873
rs546956177	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73078865	TACGACTAGAGGCAT[A/G]CGTCACCTCGCCTGG	9873
rs546971436	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029620	GGAGGTGCAGACACA[A/G]AGGTAGGAAGTCATT	9873
rs546976490	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72946711	ATAGCTACCATTTAC[A/C]GAATATCTATTATAT	9873
rs546981442	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72974655	CAGAATTTTAAAATG[C/T]ATTTATTTTTAGTTA	9873
rs546982761	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932567	GAGCTTTCACACAGG[C/T]TTTTCTTCTGCCTTG	9873
rs546992185	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990896	AGACACAAAAAAACC[C/T]TTCACAAAAATCAAT	9873
rs547004494	in-del	-/A	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73085801	TTCAAGTTGATGTTT[-/A]AAAAAAAATGAGAGC	9873
rs547010245	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73021966	GGTCTTAGCTACTTT[C/T]GTGTATGGCAGGAGA	9873
rs547013467	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73025070	GCTCAGGCATTGTGG[A/G]AGACTGTCATGATTC	9873
rs547020105	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72871432	TTGCTTAGCAAGTAA[C/T]GCATTCAGCTTCATT	9873
rs547028531	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876650	TATTCTACTCATATG[C/T]AGTGGAGTTCGATGA	9873
rs547053247	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72867782	TCTTTTTAAAAAATT[C/T]TGGCTATTATTAAGT	9873
rs547066789	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72868268	AAACCAAACACTCCA[C/T]GTTCTCACTTGTAAG	9873
rs547075919	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033223	AACCCGGGAGGCGGA[A/G]GTTGCAGTGAGCTGA	9873
rs547078315	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008686	TTAAATTTATCCCAT[C/T]GGCAAGGAAAAACAA	9873
rs547081894	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071160	CATTCTGGAGCTGCT[C/T]TAACTAGCTAATACC	9873
rs547086209	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978779	TGTAAGTTTCCTGAG[A/G]CCTCCCCAGCCATGC	9873
rs547088835	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913683	TCTCCTTTTTCACTT[C/G]TGATTTTATTTATTT	9873
rs547091456	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72850006	CCTTTTAACTCTGCA[C/T]AGAAATGACTATCTT	9873
rs547122485	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962377	CAAATACATTAAATA[C/T]CAATAAGTATAACCT	9873
rs547134476	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73014998	ACAGGTGCCCGCCAC[A/C]ACACCTGGCTAATTT	9873
rs547147296	in-del	-/ATC	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72970402	AGGTAATGGAAAAAT[-/ATC]ATGTGTTATAGAAAA	9873
rs547164723	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142257	GGTCGGCCGCCTGCG[C/T]CGCCGCTCCCGGCGG	9873
rs547171209	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72907504	TTATTTTGAGATATG[G/T]TCCAACAATACCTAG	9873
rs547186685	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72997631	TGTACCAGAAATATG[G/T]AATGTAGTATTTAAA	9873
rs547189216	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73061070	CTCCCAGCAAGATCC[C/T]CGCAGAAGGCAGATG	9873
rs547189536	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125869	ATAAAACACTTCTTT[G/T]AGTAAAACAGAGCAA	9873
rs547190580	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863716	AAGAAAATATACAGA[C/T]GCAAATAAACATATG	9873
rs547197774	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73006682	CTTGGCCCTCTGTAT[G/T]CTCCCTACTATGCTT	9873
rs547199252	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72852485	GGTGGTGCCAAAATG[A/G]CGAAACCTTGTCTCT	9873
rs547203557	in-del	-/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72862682	ATGCAGTCATCATAA[-/T]TCCTAATAAAAATCC	9873
rs547209700	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961503	TCAAGTGATTCTCCC[A/G]TCTTGGCCTCCTAAA	9873
rs547214419	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72963152	GTTTTTAAAAAAATA[C/T]TGTCTTTGTTTCACT	9873
rs547219290	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108296	GCTCATTACATATTC[C/T]AGTTACTAATCCCTG	9873
rs547245435	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954985	ACTCACCACTCAACA[A/C]AATACTTCTGACTTC	9873
rs547251944	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052804	GATGCTAATAGCATG[A/G]AAAGATCAGTTTCTA	9873
rs547252482	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115070	CAATTTAGCCTGCAG[C/T]GGCAAGGCGTGCTGA	9873
rs547271105	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72955981	TAAATATCATCCTCC[A/G]CTAAAAGGAAACAGG	9873
rs547275684	in-del	-/GTT			intron-variant	FCHSD2	GRCh38.p7	11:73100376	GTTGTTGTTGTTGTT[-/GTT]TTGAGATGGAGTTTC	9873
rs547276147	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73123766	CAAATGCAGTCTAAA[C/T]AGAGCTGCCTTTTCT	9873
rs547276478	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72880710	CCCTTGAGCCCAGGA[A/G]TTCGAGACCAGTCTG	9873
rs547288674	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73063739	CAGCAAGAAGAGCTA[A/T]CTATCCTAAATATAC	9873
rs547289366	snp	C/T	0	0	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840699	GTAGATTAAATGTCC[C/T]GAGATGAGTTGATTT	9873
rs547302453	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855897	TACATCTATACTCTT[G/T]GAACTATTAGAATAT	9873
rs547302943	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104414	AGCTGGGATTACAGA[C/T]GCACACCACCATGCC	9873
rs547314712	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72950387	GTGTTTTTGGTGATA[C/T]CTGAGAAACTGTTGC	9873
rs547317270	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944736	TGTGCAAAAATCACA[A/G]GCATTCTTATATACC	9873
rs547325925	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73119040	GGCGCGGTGACTCAC[A/G]TCTGTAATCCTACCA	9873
rs547326220	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111195	GGTCCATTCGGTCTA[C/T]AGTACAGATTAAGAG	9873
rs547333004	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72986080	AGCAGCCTCTTATTT[C/T]TCTAACAAGAGAAAA	9873
rs547341194	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72977812	GCAATCCCATTACTG[G/T]GTATATACCCAAAGG	9873
rs547342347	in-del	-/CA			intron-variant	FCHSD2	GRCh38.p7	11:72845462	AAAAAAAAAAAAAAA[-/CA]ACAACAAACAAACAA	9873
rs547361381	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72924096	GAAAGTTTCTTTTGA[C/T]GTACAAAAGTTTTAC	9873
rs547388303	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986770	GGTAGGTATTAGTGA[C/T]AGATAGAATAAAATA	9873
rs547388444	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878962	AAATACAAAAAAAAT[C/T]AGCTGGTTTTGGTGG	9873
rs547414706	snp	C/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73025276	GGATAAAGAAAATGT[C/G]GTATATATATACCAT	9873
rs547419584	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947887	TTTTACATATTATTT[A/G]TGATTCTCATTTTAA	9873
rs547426990	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72871018	TTATGATGTGGCTGG[C/T]AGAAATAGCAGAGAT	9873
rs547427070	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879690	AGGTTTTAATAGACA[A/C]TAATAATAACTCATC	9873
rs547433969	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896502	TACATAGGGCAGAGA[A/T]GTTGAAAAGTACAAG	9873
rs547457366	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72940940	GAAGAAATCCTGACA[A/C]CCAATGGATCACCAA	9873
rs547468426	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72988473	ATATATACACTAGAT[C/T]TTTGTGTAAAAGAAA	9873
rs547472452	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72880590	ACCATATATAAAAGT[C/T]GGCTCAAAATGATTA	9873
rs547475472	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73026131	GGTGTGTGCCACTGC[A/C]CCCAGCTCATTTTTT	9873
rs547476261	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72906274	CACTTTTTGATGGCG[C/T]TGTTTTTTTCTTGTA	9873
rs547483419	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73115616	GAGAGAGAAGGCAGA[G/T]AGCTAGACACAGACA	9873
rs547504717	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73136748	AAAAACCCAAGTTCG[C/G]GCCAGGCGCAGTGGC	9873
rs547521724	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72888440	GGGCTAAAAAGTAAG[C/T]GGGAGGTGAGATTCT	9873
rs547560553	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144074	CTCAGCTCCACCACC[A/T]ATTTATTGTGAAGCG	9873
rs547569192	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909803	CCTCTGCCCGGCCGC[C/T]CCGTCTGAGAAGTGA	9873
rs547586322	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73055581	AATAATATTTATTTC[A/G]TTAAGATTTTATGCA	9873
rs547591820	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73122579	TTAAATTTCCTTTGT[C/T]AAATCAAATAGGCAA	9873
rs547612539	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034806	TTTGACCAGAACTTC[A/G]AAGCAGCAAAAGAAA	9873
rs547644779	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980506	TAACGAGGATAACAA[A/C]GAAAATGAGAAAGGA	9873
rs547646169	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910118	GGCCACCCATCGTCT[A/G]GGAAGTGAGGAGCAC	9873
rs547652239	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121732	TGCCACTGTAAACAA[C/T]AGCTATAATTTATAA	9873
rs547654980	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73051547	GGCAGAGGTAGTAAA[A/C]CAAACAACAATGAAA	9873
rs547657920	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73121355	AGTCCATTATTCCCA[C/T]TCTACACAGATGAAG	9873
rs547662138	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856415	CTCTCCTCTTAACCA[C/T]TGTTTGCCTAATACA	9873
rs547672561	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027769	GCCCAGGACCAGGGC[G/T]GTGCTGCTCTGTGCA	9873
rs547696275	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72909912	GAGGAGCACCTCTGC[C/T]CGGCTGCCCATCATC	9873
rs547715206	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129949	GTGTGATCTCAGCTC[A/G]CTCACTGCAAGCTCT	9873
rs547725094	snp	C/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72865731	TTCAAAGAATCATGA[C/G]ATTCTGGAGTTGGTG	9873
rs547735822	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72904311	CTAAGAGGATCACCT[C/T]TCTAGTTGCCAAACT	9873
rs547769705	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72870006	TGTTTCTTTCCACAC[A/C]CCCCTATGCTCCCAC	9873
rs547776300	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73091441	GTAATCCCAGCTACA[C/T]GGGAGGCTGAGGCAG	9873
rs547777477	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73079434	CGAACTCCTGATGTC[A/G]TGATCCGCCCGCTTC	9873
rs547779801	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73129306	CCCAGGCCACGGACC[A/G]CTAACGGTCTGTGGC	9873
rs547787051	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72857562	TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGGGACT	9873
rs547788844	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112985	ATGCCCTTTTGCAGC[A/T]ACTTTCTAGATCTGG	9873
rs547793044	snp	C/G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72911263	CTTTCTCCAATGTAT[C/G/T]TTCTTGACAACTTTG	9873
rs547810415	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991099	CTCTACGCAAATAAA[A/C]TAGAAAATCTAGAAG	9873
rs547814946	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72872193	TTGCAAAAATCTGCT[C/T]ATTCTTTTCATAATT	9873
rs547822299	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048605	ATCTGAAGTAGTTAC[C/T]TGGGGCAAGTTCTTC	9873
rs547822347	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041233	TGATTTCCTTTCTTT[G/T]GATAAATATCCAGTA	9873
rs547828865	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114916	ACAAGTACTCCCTCG[A/G]ACGCCATGGCTGGTG	9873
rs547843586	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034143	GAGGTTTGTTACATA[C/T]GTATACATGTGCCGT	9873
rs547851905	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72980005	CCTAAGAAGGCAGGA[A/G]GGGATGAGATATAAT	9873
rs547866977	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883761	CATGGTGAAACCCCA[C/T]CTCTACAAAAAAATA	9873
rs547884777	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041954	TGTTTTTGAGACAGA[C/G]TCTCACTCGTCACCC	9873
rs547891735	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113899	TTCTCTATATTACTA[A/G]GCAGAGATTCTTGTT	9873
rs547919718	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72934072	CATGATCGCGCCACT[A/C]CACTCCAGCCTGGGC	9873
rs547931074	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944619	CAAATTGTCCCTGTT[G/T]GTAGATGACATGATT	9873
rs547948361	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72950918	CGTGACTAATTCTCT[C/G]TAATTCAGTGTGAAC	9873
rs547952731	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72884483	ATTAGAAATATATAT[A/G]TATCTGTGTGTATGT	9873
rs547965712	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73118750	CTGAGCCCTTACCAC[A/G]TGTAATGCATTGTTC	9873
rs547965752	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73059240	GGCTGAAGACTTTAC[A/G]TTACACTGTGTGAAC	9873
rs548001939	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72926920	TTATTTAACATAAAA[A/G]AGTGAAAAAAATGGC	9873
rs548003355	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73113854	TTGTAGTGGTACTGC[C/T]TTAGTGGTCTTGGTT	9873
rs548009223	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73048635	CTTACAGTAAGTGCC[A/G]GAAGTACGAAAAAGC	9873
rs548014987	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72986268	AGGTCGGAGTGCAGT[C/G]GCGTGATCTCTGCTC	9873
rs548019605	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113750	TGGGAAAGTTTGTCA[A/G]GTATCTGAAGAAACT	9873
rs548034236	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023654	AGAGACTTCCACAAT[C/T]ATGTTCTAGGTATTT	9873
rs548038848	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072581	AACAGTAAGATTTTA[A/C]AAAGTAATTTACAAA	9873
rs548053186	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120655	AATCATTTCATCTTG[C/G]AAGGCGGAGGCTGCA	9873
rs548061512	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72868517	CCTGCACACGTATCC[A/G]GGAACTTAAAAGTTG	9873
rs548062516	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72883710	GCCAAGGCAGGCAGA[C/T]TGCTTGACCCACGAG	9873
rs548063214	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73064866	TGAGGCAGTAATTAA[C/T]AGCCTACCAACTAAA	9873
rs548063357	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72972058	ACCTCAATAAAATTG[A/G]TTTAAAAAGAGTTAA	9873
rs548087861	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72918274	TTTATTAGCTCTATT[A/C]GTTTTTTTAATGGGC	9873
rs548095412	snp	C/T	2.39043e-05	0.0034571	intron-variant	FCHSD2	GRCh38.p7	11:73015905	TAAAAAATACATATT[C/T]TTTCTAAAATAAATA	9873
rs548102549	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73073509	TACTTTGCATGTGCT[C/T]GAGATAAAATTTTCC	9873
rs548104170	snp	C/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72850516	CCACCACCACGCCCG[C/G]CTAATTTTTTGTATT	9873
rs548104928	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72964344	GCTTAAGATGTCATT[A/G]TAACTCTTCTTTGAT	9873
rs548112813	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73083356	GAGATCGAGACCATC[C/T]CGGCCAACATGGTGA	9873
rs548122420	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129153	TGGGATTACAGGCAT[A/G]AGCCACCGCGCCTGG	9873
rs548123507	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73124526	TTTGGGAGGCCAAGG[C/T]AGGTGGATCACCAGA	9873
rs548129955	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900175	TATACATAACTTTCA[C/T]CCCAACACCAGGTCC	9873
rs548130978	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73092933	GTCTACCTGGGGACC[C/T]TGTGCCACACCAAAT	9873
rs548134043	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72844927	AACCCCACTCATTTA[A/C]CCTTGATAGCTTTTC	9873
rs548144995	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956123	TATCAGTCAAGTATG[G/T]AGCAATTTGAGCGTA	9873
rs548147258	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73033555	TAGGGCGCTACACAA[C/G]ACATCTTCCACAAGA	9873
rs548158733	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73016488	TTGATATGCCTTTCA[C/T]TTTTAACTATTTGAC	9873
rs548174229	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908473	ACTGTTTTCCATAGC[A/G]GTTGTACTAATTTAC	9873
rs548176656	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067998	CAGACACGAGAGAAT[A/G]AGAACCAAGTGAAAG	9873
rs548185018	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976683	GTAACCAAAACAGTA[C/T]GGTACTGGCATAAAA	9873
rs548195704	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923008	CCTCTATGGATTTGC[C/T]TACTCTGGATATTTC	9873
rs548203922	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73128978	CCGGGTTCAAGCGAT[C/T]CTCCTGCCTTAGCCT	9873
rs548211131	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908944	CAGGTGTGAGCCATT[G/T]CATGTTGCCCTGTCT	9873
rs548216744	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72891048	CAGCCTCCTGAGTAG[C/G]TGGAACTACAGGTGT	9873
rs548219793	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044246	TGCCTCACTTATTAA[C/T]GCTGAATTCCTCAAT	9873
rs548240268	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061190	GGTGGGGGGTCACCT[C/T]ACCTGGGAAGCACAA	9873
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	9873
rs548270288	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73044738	ACATAGTACATGCAA[C/T]AATTTAACATTCTAG	9873
rs548272593	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093253	CCCTGTACACCTCTT[C/T]CCTTGGCTGATTTTA	9873
rs548275819	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73086175	CACTTTTGAGAGATA[A/G]AGGTGGGTGGATCAC	9873
rs548276498	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936933	GTATGGACTTCCTTG[A/G]AGACAGTTTCTCTTG	9873
rs548277054	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121554	CTTGGGTTGCTAAGA[G/T]TTAAATGAAATAATA	9873
rs548281094	in-del	-/TAAAT	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73125401	CTAAGTAGACAGTGA[-/TAAAT]TAAGAATGCATGGTG	9873
rs548297236	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72901849	GTTCATTATTCCATT[G/T]ATTAATTCTATTCTG	9873
rs548298616	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72876061	ACAGTGGCTGACACC[A/T]GTGATCCCCACATTT	9873
rs548306068	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084675	TTGGGATTACTGGCA[A/T]GGGCCAACGTGCTTA	9873
rs548323250	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73045295	GAGGATGTGGAGAAA[C/T]AGGAACACTTTTACA	9873
rs548351278	in-del	-/AAAAC			intron-variant	FCHSD2	GRCh38.p7	11:73096027	TATAGAAAAAAACAA[-/AAAAC]AAAACAAAACAAAAA	9873
rs548356077	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030922	ATCTCTATACTTGCG[C/T]GTCCTGAATTTCTGC	9873
rs548369659	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062203	GCAAACTTCAGCAGA[C/T]CTGCAGCAGAGGGGC	9873
rs548387112	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72930071	ATGAAAAAAATAATA[C/T]GTTGTGAAAGTTGAT	9873
rs548398323	snp	A/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836703	GGGCCTTTTGGAAAG[A/G]TCTGTTTACCCAAAC	9873
rs548418438	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869427	AAGGGAAAGAGAGGG[C/T]TGGGGGGAGGGAAGA	9873
rs548430279	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73076528	TGATGGTTACTTTGG[G/T]CTCAGGATAAAAGTA	9873
rs548435517	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72927965	TTACTTACTTTATCA[A/T]GTTAATGATTTTCTC	9873
rs548443348	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939315	AAATTGTAACTAAGC[A/G]TTTTTCCCCCAGTCG	9873
rs548460319	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73001201	GTTGGCTAACCTTTT[G/T]CTCACAGGGCAGCAC	9873
rs548463172	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73128126	GGAGGAGAATCCTAA[A/G]AGGCCAAAATACAAA	9873
rs548473508	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73094012	GGTCAGGAGTTCAAG[A/C]CCAGCCTGGCCAACA	9873
rs548479615	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946035	ATTTGACCCAGCCAT[C/T]CCATTACCGAGTATA	9873
rs548491010	in-del	-/A	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:73133993	ATTGTACAATCCTAT[-/A]AAAAAAAAGTTGAAT	9873
rs548502233	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72967616	GAACTAGGGAGTAGG[A/G]AGAACACAAAATGAC	9873
rs548505405	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72847103	CTGGGCTCCAGTGAT[C/T]CTCCTGCCTGAGCCT	9873
rs548537887	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72851313	CAAGGTGTAAGACTA[C/T]GTATTTTAAGATGTT	9873
rs548540521	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959696	AACGCACCTGCTCCC[A/C]ATAGCTTTCTATGTG	9873
rs548547922	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894603	ATTTCAATAAAGTTA[C/T]TAATTATTTATCCTC	9873
rs548569590	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839139	ACTAAGATCCTAGCA[C/T]ATCCTCCAAAGCAAA	9873
rs548580255	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061547	CGGAGCCCAGCAAAC[A/T]AAGATCCACTGGCTT	9873
rs548601877	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73095876	ACACTATGAACAGCC[A/C]TGCAGCAGCAATCTT	9873
rs548610416	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119300	AGAGCGAGACTCTGC[C/T]TCAAAAAAAAAAAAA	9873
rs548623052	in-del	-/G	0.00159617	0.0282053	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144036	AGAGCCCAGGCCATA[-/G]GTAGCGTAGGCTGGG	9873
rs548625848	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73130744	TTCTCTGCCTAGTTA[A/G]CATCTCCTTTTTCTC	9873
rs548626109	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960186	CGAAGGCAGAGCAGG[A/C]ATGTCACAAGGGAGC	9873
rs548628649	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73045049	CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC	9873
rs548632227	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853477	TGGAGTGTAGTGGCG[C/T]AATCTTGACTCACTG	9873
rs548637226	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73040295	AAGCTGTAATTGTTT[C/T]GCAGTCATGTGGAAA	9873
rs548648906	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908515	CAGTATACAAGGGCT[C/T]CCTTTTCTCCACATC	9873
rs548652610	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108951	TCATTCTTCTGCATA[C/T]GGATATTCAGTTTTT	9873
rs548662208	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072400	AATGAAGTTTAAAAA[C/T]TTAATTAAATTTTTA	9873
rs548668632	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72909387	TCTCGGCTCGCTACA[A/G]CCTCCACCTCCCAGC	9873
rs548669638	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000518	ATATAATTAAAGTTT[A/G]GAGTCCATCAGGTTT	9873
rs548676661	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73019920	TTTTTTAAAGTTTTT[A/T]AAAAAATTTTTTTCA	9873
rs548706214	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048819	GGGGAATGAATATTT[C/G]CTGAGCAATAATTCA	9873
rs548707383	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72945513	TCATGTCTAAAACAC[C/G]AAAAGCAATGGCAAC	9873
rs548710358	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72903814	TGGGAAAAGGGATAA[C/T]TGAGGAGACGCAAAA	9873
rs548713481	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101741	TGCACCCCCCGCCCC[C/T]GAAAAAAACACAACA	9873
rs548715335	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109605	TGGTTTTTTAGTGGG[C/G]TCTTTATGTTTCCCC	9873
rs548718362	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058187	CCTGGCCAATTCTGT[A/G]TTCTTTAAAGGTATT	9873
rs548723485	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893614	GCCACTATGCCCAGC[C/G]CAATATTTTTCCTTT	9873
rs548726152	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064816	AACCAGAAAGAAGTC[A/G]AATCCTTGAATAAAC	9873
rs548729084	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72906821	ATGCTGTTTTGGTTA[A/C]TGTAGCCTTGTAGTA	9873
rs548742695	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73012057	TACACTTTCAGTGTA[C/T]AAAAATATACTTATG	9873
rs548763299	in-del	-/C	0.0185938	0.0946107	intron-variant	FCHSD2	GRCh38.p7	11:73009364	AGCCAGGTGTGGTGG[-/C]CGTACACCTGTAATC	9873
rs548766118	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847464	CACAGACAAGGTAAA[C/T]ATACAGAGACAAAAC	9873
rs548767845	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72993417	TTACTGGGTATATAC[C/T]CAAAGGATTATAAAT	9873
rs548769087	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72905302	CTCTGTGGGTATATA[C/G]TAGGTATTTATATTT	9873
rs548777974	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102374	CAATTACACTCCTAA[A/G]TACTTATCCAAGAGA	9873
rs548784630	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112881	ATGTTAGCCAAGCTC[A/G]TCTTGAACTCCTGAC	9873
rs548801687	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73094835	TACTGCAATAGCACT[A/G]AAATGATGACCTGAG	9873
rs548813860	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885856	AAATGACTATTCATT[G/T]TACACCCTGCCCTCC	9873
rs548821112	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942432	TGTAAATGGGCTAAC[A/T]CAGGCAGGAATAGCT	9873
rs548834753	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72948791	CTGCCTCAGTCTCCC[A/G]AGTAGCTGGGACTAC	9873
rs548838430	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73039576	TGTAAGTTTGTCACA[A/G]GTGAATTTTAAAAAT	9873
rs548847090	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72868533	GGAACTTAAAAGTTG[-/A]AAAAAAAATTAGCTA	9873
rs548861592	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72897252	GGTATAGTTGTCCTT[C/T]CATATCTGTGGGTTC	9873
rs548864891	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087062	AAAAGGCATTGTATC[A/G]TAGGAGATGACAGCT	9873
rs548883044	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986305	ACCTCTGCCTCCTGG[A/G]TTCATGCCATTCTCC	9873
rs548888457	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72844992	TGCCTTGAATATGCC[-/A]AGCAAAAGGCATTTT	9873
rs548899667	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032668	GAAAGTATATGGGAA[C/T]ATAAAGCAGAGAGAT	9873
rs548909263	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72935006	TCCCTTACACATTAC[C/T]TCTGCCCTCTTTATT	9873
rs548910289	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038937	GTTCTTTTTCCAGTA[C/T]ATTTTTTTGGCTTGA	9873
rs548915910	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73064102	TCTCAGGCCACAGTG[A/C]AATCAAACTAGAACT	9873
rs548939910	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72952483	GCATGTGTCACCACG[C/T]CCAGCTAATTTTTAT	9873
rs548944467	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72935939	AAGTCAGATGTCTGA[A/C]AAAGGTCTGCTGTAC	9873
rs548944535	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011395	ACCTAGGCTAGCAGG[C/T]GGGGAATACTTGCCC	9873
rs548956591	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72929460	CCTTCTGGCCTGGGT[A/G]GATTATTGCTAGTGT	9873
rs548959432	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72979556	GCTTTGGATTCTCAA[C/T]ACTTACACAGTAAAG	9873
rs548964330	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132292	ATAACAGTAGCTACC[A/G]ATGCTAAATACCTAC	9873
rs548973502	in-del	-/CC	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73072993	TTAAGCAAGGAGCCG[-/CC]CCCTTAAAGTCCACA	9873
rs548977116	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72972416	TTCAAGGTGCCCTAG[A/T]ATTCAGCCTGATGCC	9873
rs548992252	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989659	CCAACTCCGTGGATA[A/C]ACATATACATTCGAG	9873
rs548994050	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72904628	TTTAAGAAAATATAT[A/C]CATATTACAATTTAC	9873
rs548995394	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083506	GTGAGCCAAGATTGC[A/G]CCACTGTACTCCAGC	9873
rs549001315	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73131368	TAAAAGTACAAAAAA[A/C]AAAAAAAAAAATTAG	9873
rs549025670	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139868	AGGAAAAAGTTTGTA[A/T]TGTGTTAGTTCCAGT	9873
rs549029605	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856573	AAATTATATATTTTT[C/T]CTGACATATTTATTG	9873
rs549059424	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73139933	TTAAAGCAGGAAATC[C/G]AAAAGGAAATTCCAT	9873
rs549063034	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138752	AGCTAGGACTACAGG[C/T]GCACGCCACCATGCC	9873
rs549075748	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104623	ACCCAGGCTGGAGTG[C/T]AGTACCGCAATCTCA	9873
rs549078184	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73105121	TATTCCCATTCCATA[A/C]ATGAGGAAAGTACAA	9873
rs549079776	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981350	AATCTGTGAGCTGGC[C/T]AGGCCCTTTAACTTC	9873
rs549083542	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73115824	TAATTGTGAGACATA[C/T]CCACATTATTGAGGG	9873
rs549090482	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956568	TGAGAAATCCAAGAT[C/G]AAGGCGCCAGCAGAT	9873
rs549091095	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72849527	TTCAATGAGGAGCAG[A/G]GGACAACCAACTGAG	9873
rs549094870	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72857478	AGTTTCACTCTTGTC[A/G]CCCAGGCTGGAGTGC	9873
rs549101212	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73003688	AGACGGGGTTTCACC[A/G]TTTTAGCCGGGATGG	9873
rs549102924	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73070748	CAAATTAAAAAAAAA[A/G]AAGAAATTGAACAAG	9873
rs549113684	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73102188	ATACCACTGAACACC[C/G]ACTAGAATGACTAAA	9873
rs549115079	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73027979	CTAGATTTCAGAGAA[A/T]GTATGGAAACACCTG	9873
rs549116689	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875198	TTTACTTGTAGAATA[C/G]AATCAATAATGGTAG	9873
rs549123297	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905773	GGACATGAACTCACC[C/T]CTTTTTATGGCTGCA	9873
rs549124526	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72977097	ACCTGGCTAATTTTT[C/G]TATTTTTAGTAGAGA	9873
rs549126055	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138278	TACAAGTCAGCACAG[A/T]TATCAGGACACAAAC	9873
rs549127097	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004616	ATGTATGCCCTTTTT[A/G]CCCTTGCCTCTTTCT	9873
rs549141327	snp	C/T	0.0433635	0.140717	intron-variant	FCHSD2	GRCh38.p7	11:73097633	TTTTTTTTTTTTTTT[C/T]CTAATTACTGATTCA	9873
rs549145077	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122871	ACAAAGAATCTACAA[G/T]ATATGCAGATTAAGT	9873
rs549152619	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73074436	ATCCTCACCCCAATA[C/T]AATATCACATACGAA	9873
rs549161982	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042135	TTTCACTGTGTTGGC[C/T]AGGCTGGTCTTCAAC	9873
rs549178765	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73105890	TGTATTTCAGGTCTC[C/T]AATAAATCTGACAAA	9873
rs549187515	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72966263	CTCCCGGGTTCATGC[A/G]ATTCTCCTGTCTCAG	9873
rs549189500	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73093315	CCTTACTGAGTAAAC[A/T]TTCAGTGAGCTCTGA	9873
rs549193468	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137744	AAAGACAACAGCATA[C/T]ACAGGGGCATGAATG	9873
rs549204940	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897936	CTTTCTGGTATCATC[A/T]GAGAAATGATAATTG	9873
rs549207005	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72988892	CATGCTCACTACTAA[C/T]AGAGAACAAACTATT	9873
rs549207381	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72904798	TAGTTTCTTCATCTA[G/T]CTCTCCTTTCCTCCC	9873
rs549217934	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106816	AACAACAGACCAGAG[C/T]CTCCATGTGCAGTAG	9873
rs549224325	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958673	TCCACTTTCTCCTTT[C/T]ATTAAAAATCTACCT	9873
rs549225814	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997431	AACATCTTCCCAGAG[C/T]CTCTACAGTTTTTAT	9873
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	9873
rs549244242	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889193	GTCTCGATCTCCTGA[A/C]CTTGTGATCCACCCA	9873
rs549256890	snp	G/T	0.00795532	0.062565	intron-variant	FCHSD2	GRCh38.p7	11:72851658	TGAGGCAGGAGAATT[G/T]CTTGAACCTGGGAGG	9873
rs549259384	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73037589	CACAATATTCTTGTC[A/G]TCTTTAGATATTCTA	9873
rs549263625	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066550	ACTATCATCAGAGTG[A/G]ACAGGCAACCTACAG	9873
rs549270391	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116589	TCTGCCACCCATGCT[A/G]GAGTGCAGTTGTGTG	9873
rs549271057	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998265	TTAATTTGGACCAGG[C/T]GAGGTGGCTCATGCC	9873
rs549281553	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73107299	GTGATCTGCCCAGCT[C/T]GGCCTCCCAAAGTGC	9873
rs549286687	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73018361	TTACTATTTGTGTCT[C/T]TTTCTAAAACGCCTT	9873
rs549292990	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72974801	TCTCTCCAAGAAAGA[A/G]GGCATTAAAAAAAAA	9873
rs549325439	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091564	AAAAAAAAGAAAAAA[G/T]AAAAGAAAGCAAATA	9873
rs549336915	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086200	GATCACTTGAGGCCA[A/G]GAGTTTAAGACAGGC	9873
rs549346185	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73084883	AGTTTAAAGACTTTA[C/T]CGTTATGTGCCAGGA	9873
rs549349834	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73036106	ACTAAAGGCTAAGAG[C/T]AGACTGGCTTGGACA	9873
rs549364413	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73139025	TCTTGATATATCCAG[A/G]TTGGATGAGAATAGA	9873
rs549369053	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882152	CGTCTCAAAAAAAAA[C/G]AGAGCAGAGGCTGGG	9873
rs549370117	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950619	GTTTTAGTACCTTTG[C/T]TGACAATCAGCTACT	9873
rs549370403	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982100	TATTTTCTAACCTGT[A/G]TTCTAATAAGCAGAA	9873
rs549371115	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72990250	AGATCTGTGTTTCAA[C/T]AGAAACCTGATGAGA	9873
rs549380023	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72861743	AAGACCAACCTGACC[A/G]ACATAGAGAAACCCT	9873
rs549384770	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73073811	CATAAAATCAAATAA[A/T]AAAAACTGTACATGT	9873
rs549404359	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882867	GGCAATGAGAATAGT[C/T]CAAATAATTCTAAAA	9873
rs549404584	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860235	CATGGACCGGTAAAA[C/G]GTTCGTTCCAGTCTA	9873
rs549409373	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72967185	AGCCTGGGCGACAGA[C/G]CAAGACTCTGTCTCA	9873
rs549416700	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844380	AAGGAAATGATTGAG[A/G]TCAGTCATGGTTTGG	9873
rs549434845	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72899322	CAATCCAATAAAAAA[A/G]TAGAAACAAGGTTTG	9873
rs549442263	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977706	ATGTGAAGAAACAGG[A/G]ACACTTTTACACTGT	9873
rs549442512	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72968255	AACAAATGAAAATAA[C/T]TACAGATAAATAACA	9873
rs549449667	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029017	GAAAACGGACTAACA[C/G]AGGAAGCATGACATA	9873
rs549453627	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73021084	GGTCTCGCTATGTTG[C/T]CCAGGTTGATCTGAA	9873
rs549466266	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72919548	GTCCAATTTCCTCCA[C/T]ATAAAATGAACATGG	9873
rs549470844	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73003263	AACTGGCAAATGGAG[A/T]AATAACAAAAATACC	9873
rs549474438	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72867767	ACTAGCAAACTATTA[G/T]CTTTTTAAAAAATTT	9873
rs549487298	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73013814	ACCTGAATCCTGAAT[C/T]TTAAATAAACTTGGA	9873
rs549511801	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023195	AAAAATGATAAATTG[C/G]ACCTTATCAGAATTA	9873
rs549512977	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021890	GCCCAGGCAACACAA[A/G]GAGACCCCTGTCTCT	9873
rs549549271	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986228	TTATTTATTTATTTA[A/G]AGACGGAGTCTCGCT	9873
rs549558305	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72865569	TACTAGGCACAGCTC[C/T]TTCATTCCCTTCCTT	9873
rs549574408	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022869	GTGGAACAAAAGAGA[A/G]ATCCCAGAAATAGAC	9873
rs549576009	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931782	AAACACAAAAAACTC[C/T]TCTTACATCTTGCAT	9873
rs549592705	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72913024	AGGGGAAGCAGCTTT[A/G]TCTTACGTGGCAGGA	9873
rs549597815	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863006	TAGTTCGCTGTAACC[C/T]TGAACTTCTGGGTTC	9873
rs549602631	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72878922	GACCAGCCTGGCCAA[C/G]ATGGTGAAACCCCGT	9873
rs549620705	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72924051	TGCAAATATTTTCTC[A/C]CATTTTGTGGGCTGT	9873
rs549631301	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913565	TGAGCCATCACACCC[A/G]GCCCTATTTATCCAT	9873
rs549656632	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006543	CACTGTGACTACCCC[A/G]CTTTGAGCCACCCTC	9873
rs549659237	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863583	CAGACTAGAAGAAAA[C/T]TGCATAAATCAAATA	9873
rs549661132	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72855086	CGAAACCAGTCTGAC[C/T]AACATGGAGAAACCC	9873
rs549681651	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110385	TGTTATTGCTCTGTT[C/G]AGGTTTTGGATTTCT	9873
rs549695587	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951323	GTAAGCAGTGATGAA[A/G]CAGATGCTGCAGATT	9873
rs549696152	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982253	GAAGGTCCCGAGAAC[G/T]GTCCCATCTCTACTT	9873
rs549717343	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907406	AGAGCATCCTTATCT[C/T]GTGCTGGTTTTCAAA	9873
rs549721036	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72909477	CTAGGAAGTGAGGAG[C/T]GTCTCTGCCTGGCCG	9873
rs549728217	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930924	GTACATTTTAAAATA[C/T]CTTAAGAGTGTAATT	9873
rs549728409	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002224	TAGAAGTAAAGGAAA[A/C]AACTTGATAAACTAT	9873
rs549731850	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73070887	CTGGAAGTGAAATAA[C/T]GTGGTCTGAAAACTA	9873
rs549731920	in-del	-/A	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:72986141	TACTTCCCCATTGTT[-/A]AAAAAAATTGGGTTT	9873
rs549753812	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138898	CAGGTGTCAGTGACT[A/G]CGCACGGCCTCGCAT	9873
rs549756497	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878387	AGCTCTAACAACAAA[A/G]AAAAGATAAAAAAGA	9873
rs549771342	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885713	CATCTAGAGTGCGGA[C/G]AAACAAACAACAGGA	9873
rs549780882	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72946290	TCTCAGCAGACTATC[A/G]CAAGGACAAAAAACC	9873
rs549795982	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031816	CACAGCAGCCTTTTC[A/G]CCTGGAAAAGGCATA	9873
rs549809554	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010339	TTTTCAGAATTTTCT[C/T]GTATCTCATTGAGCT	9873
rs549820205	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72923334	GGAATGGAATTGCTC[A/G]GTCATATGATAACTC	9873
rs549846535	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73078807	CACTGCAGCCTTGAA[A/G]TCCTGGACTCACGTG	9873
rs549857389	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032556	ATTGCTCAGTATTTT[C/T]AAAGCAAATGTTTAT	9873
rs549857656	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024567	ATGAATTACATGGGG[A/G]TAAATTAGAGTCACA	9873
rs549908018	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73070257	CTAACAAGCCTCTTA[C/T]ATGGCATAGGCCCTG	9873
rs549912734	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915031	CAGCATCTATAAGGA[A/C]CTTAAACAAGTTTAC	9873
rs549920566	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025237	AGACATGGAATCAAC[C/G]TAAACGCCCATCAGT	9873
rs549924307	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017143	ACATGCCACTGAGCC[C/T]AGCTAACTTTTTGTA	9873
rs549925932	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73030874	AATCCTGAATACAAT[A/G]TTATTAACTATAGTC	9873
rs549931489	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879940	GGAGGCGGAGCTTGA[C/T]GTGAGCCGAGATCGC	9873
rs549950601	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104290	TTTATTTATGGAGAC[A/C]GAGTCTCACTCTGTT	9873
rs549950812	snp	G/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72961408	TTTAAGAAGTTTTTT[G/T]TTGTTGTTGTTGTTG	9873
rs549952686	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895576	GCACATAACTAATGC[A/G]TCTATGCAAAGATCT	9873
rs549983991	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116420	AATGAGCTGGGTGTT[C/T]TTCTCATTCTGTGAA	9873
rs549986337	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009776	CTGCTAGTAGTCTCA[C/T]AGCAGTTCCTTGACA	9873
rs549989403	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840635	TCTAAATCACTTTCA[A/T]AGCCATCATCTTGCA	9873
rs550024701	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062255	AACAGAAAGGAATAG[C/T]ATGTGCACTCAAACA	9873
rs550038627	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909341	CTCACTCAATGCTCA[A/T]TGTTGCCCAGGCTGG	9873
rs550041814	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953608	GACATTATTCCAGGT[A/C]CTGGAGACACTGCAT	9873
rs550044829	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115697	GACAAGTCCAAAATC[C/T]GTAGGGCAGGCCATC	9873
rs550058038	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847794	TCCTCCTGAGTTCAA[C/G]TGATTCTCCTGCCTC	9873
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	9873
rs550070051	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916818	TCTATGTTTTCTTTC[A/G]TTACTTGTGCTTTCA	9873
rs550072693	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902881	TAGATCAGATTTGGG[A/G]ACTGGACAATATATA	9873
rs550081261	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987788	TGTTCTAGGATCTCT[A/G]AAAGTTTAAGAAAAC	9873
rs550085316	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933342	TAGGAAAGAATTAAA[C/T]CAACTCACAGAGAAA	9873
rs550087716	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73062908	ACCTAGCAAGACAGG[C/T]CAATATTCAAATTCA	9873
rs550089321	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73082071	GGCTGGGCGCGGTGG[C/T]TCATGCCTGTAATCC	9873
rs550092834	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73071418	TGTCCAGGACTGGGC[A/G]CAGTGGCTCACGCCT	9873
rs550105836	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122835	ACAATAGCTTTATAG[C/T]GTGGCTGTTCTACTA	9873
rs550106820	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72865773	TGGGAATCTCAGAGT[A/C]TTTTAATCTTTCTTT	9873
rs550107126	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894802	AATAAGAGGTTATTT[A/G]TAGTTTTTTCTTTCA	9873
rs550121365	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73130518	AAACTATCTTCACCT[A/G]CCTTGGGCTGCAATG	9873
rs550124059	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909732	CCTGGCCGCCACCCC[A/G]TCTGGTAGGTGAGGA	9873
rs550128242	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72946117	TTTATTGTGGCACTA[C/T]TCAAAATAGGAAAGA	9873
rs550129689	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73103428	AGATTTAATTAGACT[C/T]AGTTTAGGTATCCTC	9873
rs550150395	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047071	ATATAAAAGACAAGA[C/T]GCAGAATAAATGTGA	9873
rs550154234	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73095720	CAACAACAAAAGCAG[A/G]GAACATGGGCTGGCA	9873
rs550168953	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121827	CTGGGCTCCACTCTC[A/T]GAGTTCCTGATGCAG	9873
rs550182757	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138156	TAGATGTGTGCCACA[C/T]CTCATATGTATTGTC	9873
rs550189207	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096133	TAAGAGAAGAAGAAA[C/T]AGAACAGGAAAAACA	9873
rs550200531	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72873169	CCCATCTCTACTAAA[A/C]ATACAAAAAATTAGC	9873
rs550202718	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72898945	AGAAAGGGTTTCGCC[A/G]TGTTGCCCAGGCTGG	9873
rs550213607	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040617	TACATAATAATTGTA[C/T]ACATTTAAGGGGCAC	9873
rs550214640	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72844216	ACGAGAAGGCACTGA[A/C]TTGGAACTGCTACCA	9873
rs550217761	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72933621	TGTCTTTTGGTTGCA[C/T]TGTAAGGAAAAAAAG	9873
rs550231972	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896364	TAAGTTTTGTGGACA[C/T]GCATGTTTCCCATAT	9873
rs550239710	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890283	AAAATGTATTCATGC[C/T]AACCTACTATGGTGA	9873
rs550253328	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72977500	TAGGAAAAAAAAATC[A/T]AATAATCTGATTTTT	9873
rs550276611	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73138633	TTTTTTTTTGAGACA[A/G]GGTCTCACTCTGTTG	9873
rs550277848	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126904	TTTGCCGAGCATCGT[A/G]TTGCACACCTGTAAT	9873
rs550282039	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843610	ATCATGACAAAAACT[A/G]GGGATCAAAATATTG	9873
rs550292151	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72932813	TCTGTGTTGAGCATA[A/G]GGTTTGGCATACTGG	9873
rs550317500	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141699	AAGGCAACTCACACG[C/T]GCGCCCCCCACCTGG	9873
rs550324800	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978994	CCCTGAGTAGCTGGG[A/C]CTACAAGTGCATGCC	9873
rs550327474	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890945	TTAATATAGAAAGCA[A/G]CAAAATTGTAGAATG	9873
rs550331048	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73045546	ATGATAGAATGGATT[A/C]AGAAAATGTGGCACA	9873
rs550333086	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73004218	TTACATTTATCATAT[A/C]ATTTAATCCTCATCG	9873
rs550338449	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940721	GCAGAAAACGCCCAG[C/T]TCCTAAGGGTGCAAC	9873
rs550351068	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73066684	GCAAAGGATATGAAC[A/T]GACAGTTCTCAAAAG	9873
rs550352044	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73037194	GAGTTCCCATGTATC[A/T]CTTGCCCCCACACAT	9873
rs550362944	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088638	CACATTCATAAACAT[A/G]TACACACACTTTTTT	9873
rs550368186	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72883588	TAGCCAAATGCAATT[C/T]AAAACCACAGTGAGA	9873
rs550371555	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043306	TAAATCACTAAAAGG[C/T]TCGGTCAAGTAGTGA	9873
rs550384765	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73141147	CGCAGCGGGGAGACT[C/G]ATGACAAGCCGGGTG	9873
rs550385021	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72846462	TGGGATTACAGGCGT[A/G]AGCTACCGTGCCCAG	9873
rs550394575	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73078235	TGGAACTCTCATACA[C/T]TGCTGGTGAGAATGT	9873
rs550412259	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73099256	ACTTCCTACCCACTA[A/G]GATGGCTGTAAAACA	9873
rs550458050	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72926826	ACTGAACTTTTGTTG[A/G]TAGTTTTGAATTTAG	9873
rs550477293	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030894	TAACTATAGTCCTCA[C/T]GATACACATTATATC	9873
rs550481058	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72873873	GTAAAACAAAACTGA[A/C]GCTTAACCAATCAAA	9873
rs550487828	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928439	GGAAAATGACATTCA[C/T]TTTCATGTTCCCAAA	9873
rs550488055	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73132667	ATCTCTACAAAAAAA[C/T]ACAAAAATTAGCTGG	9873
rs550496289	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72967795	AATTTTTTTTAAAAA[G/T]AAGTGGGCAGAGAGG	9873
rs550503278	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72906640	ATTTAAGCTTTCTAC[A/G]TATAGCTAGCCAGTT	9873
rs550513157	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73111409	TGTCTGATATATGCA[G/T]AGCTACTCCTGTTCT	9873
rs550529441	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963516	CTTCTTTAGCCATTA[C/T]GCTGTGTGTGATTAA	9873
rs550558821	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72913762	TTCAACAGTCAAGCC[A/G]AGAGCCAAATTACTA	9873
rs550568010	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118731	TGATGATGGCAAACA[A/C]TAACTGAGCCCTTAC	9873
rs550579142	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102333	AGTTTCTTTTAAATT[A/T]AACACACATTTGTCA	9873
rs550587176	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73126074	CGGCCAGGTGCGGTG[C/G]CTCACACCTGTAATC	9873
rs550595965	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72914103	CGCTGCAAACTGCGC[C/T]TCCTGGGTTCAAGTG	9873
rs550600291	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075504	GCAAACACAATGCAA[A/G]GCAGAAATGCAAAAT	9873
rs550609119	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950557	ATGTGGATATTCAGT[C/T]GTGCCAGTACAATTT	9873
rs550622423	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73032590	CTTCCTAACTGAAAA[A/G]AAAAAAGCACAACAA	9873
rs550646804	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73061167	CCATGGAAGGCGAGC[C/T]GAAGCAGGGTGGGGG	9873
rs550663559	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73067385	ACCTAACATAGGTGA[C/T]GGGTTGTTGGGTGCA	9873
rs550669185	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73117164	TAACAAATACATTCT[A/G]CATGTACTAACATAT	9873
rs550677449	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73015123	TGCTGGGATTACAGG[C/T]GTAAGCCACTGCCCC	9873
rs550680004	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044165	ACCTTTGTATAAATC[A/C]AACAAAGAGACCATT	9873
rs550704957	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091796	TGTAATCCCAGTACT[C/T]TGGGAGGCCGAGGCA	9873
rs550710205	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061485	CCCTGGAAAGGGGTG[C/G]TGAAGCCAGGGAGCC	9873
rs550716143	in-del	-/ACAG	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73065715	TCCTATACATCAATA[-/ACAG]ACAGAGAAAAATCAT	9873
rs550716631	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72987543	AATAAATGAAGATAA[A/C]GTGGCATTCCTTACT	9873
rs550718318	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73136260	GTCTAATGTGCTGTA[A/G]ATTTTTTTTTAACTT	9873
rs550741952	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72890917	TTAAAATATAAATTA[C/T]CCAAAGAGGCTTTTA	9873
rs550766553	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092289	TACACCACCACACCC[A/G]GCTAATTTTTTAAGT	9873
rs550767576	in-del	-/C	0.0825414	0.185628	intron-variant	FCHSD2	GRCh38.p7	11:73082332	CAGAGTGAGACTTGT[-/C]CCCAAAAAAAAAAAA	9873
rs550771642	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73053864	TTCTTTTTCCCTATG[C/T]ATGACCATTTAAATT	9873
rs550779839	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72944892	ACCACTGCTCAATGA[A/C]ATAAAAAAGGATACA	9873
rs550790410	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983120	TAAAACGGTGAAACC[C/T]CGTCTCTACTAAAAA	9873
rs550791279	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852635	TGCCAGTGCATTGCA[A/G]CCTGGGCAACAGAGC	9873
rs550816570	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937640	GAGCCACCGCGCCTG[C/G]CCAAAATATTTTTTT	9873
rs550816652	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945483	CCATTCAGGACATAG[A/G]CATGGGCAAGGACTT	9873
rs550827205	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084653	CCTGCCTTGGCCTCC[C/G]AAAGCATTGGGATTA	9873
rs550830977	in-del	-/A	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73067755	AGGCTTTAAACCAAT[-/A]ATTCCAGCAATTGAA	9873
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	9873
rs550851944	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041591	TAATTTATGGAGTTT[C/T]TTTGTTTGTTTGTTT	9873
rs550871505	snp	C/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73093832	CTGATCTCGAACTCC[C/T]GACCTCAGGTGATCT	9873
rs550872274	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72974749	AGACAGATTTGAGAA[A/T]CATATGGTATTTATG	9873
rs550878237	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72914368	AACTACCATTGACAT[A/T]CTTTGCAGAACTAGA	9873
rs550888726	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085230	ACTAAGATTTTTTTT[A/T]AAATGTTTATTCAAA	9873
rs550897337	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73100433	CAATGGTGCAATCTC[A/G]GTTCACCGCAACCTC	9873
rs550897647	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73044852	GAGGCAGGTGGATCA[C/T]GAGGTCAGGAGATCG	9873
rs550915059	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72868337	GGGGAGAACAACACA[C/T]ACTGGGGCCTGTCAG	9873
rs550918501	snp	A/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72991958	TTCAATTAGGAAAAG[A/T]GGAAGTCAAATTGTC	9873
rs550920574	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071256	CAAATTCAATTCACG[C/T]GCATACACATGAAAT	9873
rs550931938	snp	A/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73023574	ACAGAGTACTCCTTC[A/T]ACGGTGGTGGGAATG	9873
rs550943246	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72900533	TGATAAAATAACATC[-/A]AATTAGTCATAATTT	9873
rs550951287	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916165	AAACCCTCCATGACA[C/T]AAGTTTACCTACATA	9873
rs550959945	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72975628	TATCACACATACACT[A/G]TAAATATATAGTTAT	9873
rs550973572	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846443	CCTTGGCCCCGCAAC[A/G]TGCTGGGATTACAGG	9873
rs550976279	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72898917	TGTATTATTATTATT[A/T]TTTTTTTTTTAGAGA	9873
rs550977142	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73067954	CTCACAATCATGGCA[G/T]AAGGCTAAAGCCATG	9873
rs550982044	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071744	GTAGATTATTTGAAG[A/G]GAGGGAAATGGACAG	9873
rs550985909	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131659	CAGTAAGCCAAGATC[G/T]CACCACTGCACTCCG	9873
rs550994795	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967542	TGTATGATTCCATTT[A/C]TATGAAATGACCATT	9873
rs551004542	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73073988	CTGATTCTAAAATTT[A/G]TAAGAAAATATAAAG	9873
rs551022538	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72961598	GTTCAGAAATGGATA[A/C]TTTTGAGAAATGAAT	9873
rs551029405	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72860370	ACAGTTACCAAGATA[C/T]ACGTTTATACTGGGT	9873
rs551034950	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73044170	TGTATAAATCAAACA[A/G]AGAGACCATTTTAAT	9873
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	9873
rs551042342	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959578	GTCTACTCTGAGACC[A/G]TCAATTTAGGGTTGC	9873
rs551045657	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73063883	TTAAACAGATTAATG[A/G]GACAGAAAATTAACA	9873
rs551046050	in-del	-/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72861930	AAGCGAAACGCCGTC[-/T]CAAAAAAAAAAAAAA	9873
rs551075314	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908410	CCTAGCAGTGAGATT[A/G]CTGAATCATAAGGCA	9873
rs551082311	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73107009	TAAAGCCCACTTCAC[A/G]TCTCTATTATTTTTT	9873
rs551085317	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952024	GGGCATTTTTATTTT[C/T]GGCAAGAATCAAAAA	9873
rs551085906	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027122	GGTAGCAGGCAGAGG[C/T]TGGAACAGTTTGGAG	9873
rs551088241	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955061	TACCAGCTGGACATC[C/T]TCCAGTCCAATTCTG	9873
rs551097134	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73007758	ATATGCACACACATA[C/T]ACACAAATGAATGTG	9873
rs551101442	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853422	CACTGGATTTGGCAA[A/T]GATTTTTTTGGAGAC	9873
rs551104942	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73064709	AAATACAAACTACCA[C/T]CAGAGAATACTTTAA	9873
rs551112126	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900904	AATACTTTATGAATA[C/T]AATTTGATTTTCCTT	9873
rs551116605	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141645	CTGGGGGTCTCCTGC[C/G]TTAGAGGACGGACGA	9873
rs551126021	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73124443	AGAAGAGAGAGAATG[A/G]GGCAGAAAAAAAATA	9873
rs551141869	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72874504	CTCTAGTATTCATTT[C/T]AAAACAATGAAATGT	9873
rs551151159	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019035	TGGGTTACTGCCAAA[C/T]AAGTGGCAAAATGTG	9873
rs551160316	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008508	GACAAGGAAAAAGAC[C/T]GCTTTCAGTCCAGTG	9873
rs551168331	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057401	AAAGCATTCCACCAG[A/G]ATTTCCTTACTGTGG	9873
rs551174287	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72948056	TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGTGCG	9873
rs551176790	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955779	TATAGGAACAAAAGA[G/T]TCTCTTAGTGCCCCT	9873
rs551196476	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856471	CAAAATGTCCTTCTG[C/T]ATCCCATAAATATGT	9873
rs551198672	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101527	TCACTGCAGTCTCCA[C/T]CTCCTGGGCTCAAGA	9873
rs551202523	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72910219	GCGCCTCTGCCTGGC[G/T]GCCCATCATCTGGGA	9873
rs551221482	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73045191	ATCACTGGCCATCAG[A/G]GAAATGCAAATTAAA	9873
rs551222305	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000351	AATCTCAATTTTTGT[A/G]ACTCTATTTCCAAAA	9873
rs551227157	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72964648	CTTCTGCGTTAACTT[C/G]CGAATCTACCTCTTT	9873
rs551240894	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892644	GAGTCTCACTCTGTT[C/G]GCCAGGCTGGAGTGC	9873
rs551248230	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841400	CCCTTCAGGCGAATA[C/T]GTAGGTTTCTGAAGT	9873
rs551259589	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72909071	CCCCCTCCATCTCTC[C/T]GGTCTCCCTCTGTTG	9873
rs551261597	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72849306	TGAAGACACACAGAC[A/G]AGGTACACATACACA	9873
rs551265112	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72921073	CTCACTCTCCCTGAC[-/A]AAAAAAAAAAAATTG	9873
rs551268425	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72992924	GGATCTAATTAAACT[A/T]AAGAGCTTCTGCACA	9873
rs551270948	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73097386	ATTTTATTTATTTAT[A/T]TTTTTTTTTTGCATC	9873
rs551277654	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72885024	AGTATCGATAAAAAC[A/G]AAAAACCACTGCAAA	9873
rs551286565	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73038845	CCTGATTCTAAAATA[A/G]AAGTTGAAAAAAAAG	9873
rs551289957	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139806	TAAGACTTTTAAGGT[C/T]CTTGTTTTTTCTGAA	9873
rs551321847	in-del	-/ATAG			intron-variant	FCHSD2	GRCh38.p7	11:72948450	TAGACAAATATCATA[-/ATAG]ATATTTATTATATCC	9873
rs551330313	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73089887	TAGCCATAAAAATTC[C/T]GAGAAAGAGTAATAT	9873
rs551332309	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73098239	CACAGCGTAAGTTTT[A/G]GTATTGTATATTTTT	9873
rs551335665	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042220	ATGCGCCACTGCACC[A/C]GGCTGAGATTATTTT	9873
rs551353852	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048653	AGTACGAAAAAGCTG[C/G]AAATAACTTGCCATG	9873
rs551354341	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018396	AATCACTGTATGCAA[A/C]GTATCTTCGCCTCTG	9873
rs551361546	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72979711	CCCATGCCCACTTTC[C/G]CAAGAAGGTACTGGA	9873
rs551362190	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962474	CGTTTGAGAACCTCT[C/G]GTATAAGCGATTGAT	9873
rs551363470	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125252	TTTTTTCCTTCTCTT[A/C]ATCTTTTTAAAAGAT	9873
rs551383828	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73038135	GATTGCTTGAGGCCA[A/G]GAGTTCAAGCCAAGC	9873
rs551396748	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72996435	AAATGTGAAAGATAC[A/G]GACAAAAGTATGGTT	9873
rs551401535	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980613	CACAGTCCTCCAGCA[C/G]TAAGTGATTTCCATC	9873
rs551403717	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124353	AATATGGCACATGTA[C/T]ACATATATAACAAAC	9873
rs551404461	in-del	-/AG	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73101620	TTTTGTATTTTTTGT[-/AG]AGACAGGATCTTACT	9873
rs551410481	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72873050	GTTACAAATCTTAGG[C/T]CAGGCACGGTGGCTC	9873
rs551425033	snp	A/C	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72941723	GGTGCAAGGATAGGC[A/C]CTTTCATACACTGCT	9873
rs551430778	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863761	ATTATCAGAGAAATG[A/G]AAATTAAAATGACAA	9873
rs551438572	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981207	AGGAGGGACCAACCC[C/T]TGCCTCTATTTTTAA	9873
rs551448074	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73141048	GCCTCATCCACCCAG[G/T]GCCCAGAGTAGACAT	9873
rs551460965	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73055345	GAGACCCTGTCTCGA[-/A]AAAAAAAAAAAATTC	9873
rs551462151	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934196	TGAGAAGGGCACGTA[C/T]GATGAAGATGCATCT	9873
rs551464559	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123729	CACAGAGGCTGGAGA[A/G]TATATCACCTCTCAG	9873
rs551465891	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132147	CAGCCTAAAAGAGCC[A/G]TAAGATGCATCTTGA	9873
rs551475957	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72995333	CATAAAGAAGTGCTA[A/T]ACATTCTAATAATGC	9873
rs551488452	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881627	AGTGGCCAAGATGTG[A/G]AATCAACCTAAGTGT	9873
rs551489387	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72864969	CTCTGGGATTCCTTT[C/T]TTCCAATCTTACATT	9873
rs551499475	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056725	GAAACAAAAGGTACT[A/T]CAGGAGAGCACATGA	9873
rs551499677	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864549	AGACCATCTCCAAAC[A/C]AACAAAAATACACAT	9873
rs551506563	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981986	GACCCTGTCTCAAAA[A/G]CTATATATACTAAAA	9873
rs551508544	in-del	-/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73061178	GAGCCGAAGCAGGGT[-/G]GGGGGTCACCTCACC	9873
rs551518676	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73103040	GTATGATTCCATTTA[C/T]ATGAAATTCTAGGAA	9873
rs551524100	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73011278	CTGGCAGAATGCTCA[C/G]GTGGGAGGCAGTAGT	9873
rs551524815	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73043856	GAGGCCCTAAAGGAT[C/G]TAGAAATCTCAAGAT	9873
rs551527156	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73116649	GGGCACAAGCTCCCG[C/T]GTCAGCCTCCCAAGT	9873
rs551528767	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131485	AGTGAGCCAAGATAG[C/T]GCCACTGCACTCCAG	9873
rs551549069	snp	A/C	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73014922	GATTTCGGCTCAATG[A/C]AACCTCTGCCTCCCA	9873
rs551558016	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048058	ATGAGTTATTTCTAA[A/C]AAGGCAGGAAGTTAA	9873
rs551589206	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73011866	TGAATTCCAGTGTTC[C/T]CTTGGATGATCTAGT	9873
rs551590435	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905252	CTGTGCCTGTGTCCC[A/G]CTCTCCTTTTTTTCA	9873
rs551593498	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72973867	ATGGCTGCACTGCAA[C/G]AGCTGAACTGAGTAA	9873
rs551600353	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995387	AAAAGCAGGCTCCAT[G/T]GCTACAATTTTGATA	9873
rs551602568	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940998	TGGGCTGACATCTAC[A/G]GGCCGAAAGAGCCAT	9873
rs551618779	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73013301	TTAGAATTTCTTTTA[C/G]CAAACTGTCTGCCTG	9873
rs551638133	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72850047	ATTTTTCATGTTATG[A/G]AAGAATAGAGTTTTT	9873
rs551643095	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896619	TAAGTAGAACAAAAG[C/T]CCCAAGGGACTTTTA	9873
rs551643468	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73136484	GCCCGAGAGGAGAGG[C/T]TGCAGTAAGCAGAGA	9873
rs551657222	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72970972	GGCAGCATTAATGAG[A/G]AACGTGAGATAGCAA	9873
rs551660457	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021013	TCCAGAGTAGCTGGG[A/G]CTGCAGGTGCATGCC	9873
rs551667621	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858979	CAAACTCCTACAACA[C/T]ACTGTATGAAGAAAG	9873
rs551681233	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72897123	CAGGCGTGAGCCACC[A/G]CGCCCGGCCGTCCTG	9873
rs551681522	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004834	TAATCCATTCTTCAC[A/C]CACCCTTCTACACAA	9873
rs551691933	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72967042	TCTCTACTAAAAAAA[C/T]ACAAAAAATTAGCCG	9873
rs551723862	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72912165	GACTGCTGTAGCTAG[C/G]ACTTCCAGTACTATG	9873
rs551729443	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101282	CTTTGGGCAAATCAG[A/G]TAAGTGCTAGATTTG	9873
rs551737193	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113848	GAAAACTTGTAGTGG[G/T]ACTGCCTTAGTGGTC	9873
rs551767868	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72884031	ACTAGCACTTGGTAA[C/T]TGCAAAGAGGAAAGA	9873
rs551775128	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72956843	AAAAAAAAAAACCAA[A/C]CCTAGAAGACACCAA	9873
rs551789126	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081929	CATTCAAGATCGGGC[A/G]CGGTGACTCACGCCT	9873
rs551793062	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989456	AGGCAATTCTGTATT[C/T]CCCCATAATCTTAAC	9873
rs551798874	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113107	TTGATAAATTCTGCT[A/G]TTAAGAAATTATGAT	9873
rs551802011	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72905876	CAAGTCTTTGCTATT[A/G]TGAATAGTGCCGCAA	9873
rs551815589	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934959	GCCTTTAAGCAGCCA[C/T]GTCCTTTCCAGGTAG	9873
rs551833617	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976157	AGAGTTTAAAGAAAT[A/C]TGCCTAATAATATAC	9873
rs551844220	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882102	GTGAGCCGAAATCGC[A/G]CCACTGCACTCCAGC	9873
rs551845687	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72877571	CTATTACAAGAAGCA[A/G]AAAGTCTCTTAGAGA	9873
rs551853463	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035308	TCAAGAGAGTAGCTG[G/T]CACTACAGGCACGCA	9873
rs551869333	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73034935	AAAAAGGTCACTCCA[A/C]AGGCAGCTAAAGTAC	9873
rs551879454	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72875056	TTTAACATAAACACA[C/T]ATAAGTGTAAAGCTA	9873
rs551890980	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73117325	AATTCACAATCAGGC[A/T]ATCTGGTTCAAGAGT	9873
rs551892714	in-del	-/A	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72997112	TAACAGATGACTTCT[-/A]AAAAGCAGGTGTTGG	9873
rs551915453	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72917673	GGCGGATCACTTGAC[A/G]TCAGGAGTTCAAGAC	9873
rs551918013	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72992800	GACCTAAAACCATAA[A/C]AACCCTAGAAGAAAA	9873
rs551921054	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72976777	AACTCATTTTCAACA[A/G]TGGTGCTAAGAACAT	9873
rs551921330	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028368	TAACTGCCCTGTTAC[A/G]TTTCAGACTTGCATG	9873
rs551921979	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73085387	CATTTTGGAACTAGG[A/G]GTCAACTGAAAGAGA	9873
rs551953059	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73102463	CAGCATTATTTATAA[C/T]AGCCAAAAACTGAAA	9873
rs551956828	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73031001	CACACACACATTGAC[A/G]CACACCTCCAGAAAT	9873
rs551958597	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938320	CCAAGATTTATACTT[C/G]AATTTAATGTCAGCC	9873
rs551961444	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72896028	GGGAAATTTTTGCCA[A/C]ATATTTTTTTAATAG	9873
rs551969629	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73074453	ATATCACATACGAAA[A/G]TTTACTTCAGAAAGA	9873
rs551974811	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885559	GATGGCGGGAGGTTT[C/T]GTGGAGTTAGGGTAC	9873
rs551981479	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138764	AGGCGCACGCCACCA[C/T]GCCTGGTTAATTTTT	9873
rs551997748	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73139651	GGGTTGACTGGCTCA[-/C]CCCCAGATATTAACC	9873
rs552012039	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878248	TGTGCCTGTGAATAG[C/T]CACTGCATTCTAGCC	9873
rs552014767	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73016712	TCCATATTATTAATT[C/T]TCAAGACAGATTTTA	9873
rs552039255	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72852657	CAACAGAGCAAGATT[C/G]TCTTAAAAAAAAAAA	9873
rs552044913	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965561	AAAACTCAATATTTT[A/C]ATGTATTTATTTCTG	9873
rs552053555	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862238	TCTGTTGACTCTCAC[C/T]ACTTCTATTCAGCAA	9873
rs552075437	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014234	ACTCCTGGGCTCAAG[C/G]GATCGTCCTGCCTTA	9873
rs552077555	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72957733	ATAAATTCTGGAGTA[C/T]TGAGAGGTGAGGAGG	9873
rs552084988	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066442	CATAGGCATGGGCAA[A/G]GACTTCATGTCTAAA	9873
rs552086914	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058405	CTAGATGTCATCACA[A/G]TTTGCCCATCAATTA	9873
rs552100155	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72887085	TCTGAAAATATATAT[A/G]TATATATGAATATAT	9873
rs552102071	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72850746	TTCACTGTTAAGTAC[C/T]GACTGACAAGGGCCT	9873
rs552121237	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72991784	TAAGAACTATCTATG[A/G]CAAACTCACAGCCAA	9873
rs552129654	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949566	TGCCTGGCAACCACT[A/C]ATCTACTTTCTACAT	9873
rs552130394	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062625	TGAAATACACAGCAC[A/G]AGAACTTCATGAAGC	9873
rs552137553	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937561	TCTGATCTCTAGATG[C/T]TTCCATCTCCTGACC	9873
rs552139056	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73009634	GGAAAGAATTTACTT[C/T]TCCTTCATTTATGAA	9873
rs552153744	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72884767	CCCAGCTAATTTATT[C/T]TCATTTGTAACAGAG	9873
rs552160142	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72919137	AATAAAAAAAATCTA[A/G]AAAGTGTCAAACTTC	9873
rs552160250	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73131599	ATCCCAGCTACTCGG[A/G]AGGCTGAGGCACAAG	9873
rs552160511	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997846	GCTGGGACTGCAGGC[A/G]TGAACCACCACACCT	9873
rs552164773	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892557	CTATCAAAGATCAAT[A/G]TAAATCAGGATCTAG	9873
rs552185602	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72877627	ATTATAAAGAAATCT[A/G]AAACTTTCAATAGTT	9873
rs552202053	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915645	CCAACAAGGCAAAAC[C/T]CCAGCTCTACAAAAA	9873
rs552211340	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73045154	TTTATGCAGCCAAAA[A/G]ACACATGAAAAAATG	9873
rs552216337	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961307	TAGCTCACTATAGCC[A/T]CGAACTCCTGGGCTC	9873
rs552240482	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909284	TCGAGTGATCTGCCC[A/G]CCTCGGCCTCCTGAG	9873
rs552266600	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930196	GTAATTCTCTGCAAG[A/C]CCGCTGCTGAAACTG	9873
rs552272111	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73124013	CATATGGCAACCCAA[A/C]TGTCCATCAATGATA	9873
rs552273010	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038656	AACATTGAATACAAA[C/T]GGACATAAACATGGG	9873
rs552280569	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031640	GTATCCTATTAGAAT[A/C]TGACCAACAAAGGAC	9873
rs552283956	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039864	AATTTATAGAATAAC[A/G]AATGCAAATCATTTT	9873
rs552289497	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73112880	CATGTTAGCCAAGCT[C/T]GTCTTGAACTCCTGA	9873
rs552307637	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73077558	AATGAAACCACTTAT[C/T]CATACACAAATGTTT	9873
rs552311424	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930853	ATGGGTACAAAAAAA[C/T]AGAATAAGACCTACT	9873
rs552314835	in-del	-/GTG	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72962915	TGACAGTATTACACA[-/GTG]GTGGTTAAGAGAAGG	9873
rs552316608	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895530	CTATAATCACAAGCT[A/T]GATAGGGGAACTTTC	9873
rs552328278	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73065500	TAGTATTGGAAGTTC[C/T]GGCCAGAGCAATCAA	9873
rs552332693	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73088883	TATTTAAATTATGTA[G/T]TTTTTACCCTTTTAA	9873
rs552337370	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72933260	AGGCTGAAAGATTAA[C/T]CCAAAAATGGCCTAT	9873
rs552344261	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024379	CGACTAAAGACAAAA[A/C]ACTGTATATAAACAT	9873
rs552371487	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055341	GAGTGAGACCCTGTC[G/T]CGAAAAAAAAAAAAA	9873
rs552375481	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847597	AAAGGACATTTTTGT[G/T]TCCAAAACTTTTCTA	9873
rs552376358	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72970527	AATTCTTTCCTCAAG[C/G]TCAAATTTTTTTCAA	9873
rs552422352	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73069116	AGGAGTTTGAGACCA[A/G]TCTGGCCAAAATGGT	9873
rs552434999	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046919	TAAATCAATAGGATG[C/T]AGATCAAAATATGTG	9873
rs552443561	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135012	GTGTGCGCCACCATG[A/C]ACACCTAATTTTTGT	9873
rs552454745	in-del	-/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72943709	TCACTGAGGCACTCA[-/G]AATGATACCTCACAC	9873
rs552482245	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940119	TCAGGTCTAATTCCA[C/T]AGAAGCAGGACAAAT	9873
rs552485194	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033871	CTGTATTTACCTATT[C/T]GATGACGTGACTTGA	9873
rs552496403	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143123	AAACGGCGGCACTCT[A/G]CTGCAGGGCATTCAA	9873
rs552504467	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73096435	GGGCGCCTGTAATTC[C/T]AGCTACCGGTAAGGC	9873
rs552526733	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72952915	GATAGAATTATCTGC[G/T]TTTCCTCAAGGTCAG	9873
rs552544982	snp	C/T	0.0209421	0.100162	intron-variant	FCHSD2	GRCh38.p7	11:72897915	TTTTTCTAGAAAGAG[C/T]TCTGGCTTTCTGGTA	9873
rs552550708	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062225	CAGAGGGGCCTGTCA[C/G]AAGGAAAACTAACAA	9873
rs552565207	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142203	GGGTCTCAGCCGGCC[A/G]GGCGGCGGGTTAGCC	9873
rs552569019	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73049077	TAAAAAGTCCTGCCA[C/T]GGGTTCAGCGTAGGA	9873
rs552583954	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73052044	AGGAACTGGTTAATG[A/G]CATGGAAGACCAATT	9873
rs552612182	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933734	ATCTCAAAGCTTAAA[G/T]TAGACAATTTTTATG	9873
rs552625457	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846323	GTAGCTGGGATTACA[C/G]GTGCACACCACCATG	9873
rs552632603	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042187	CCACCTCAGCCTCCC[A/C]GTGTTGGGACTACAG	9873
rs552646398	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086322	GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGAG	9873
rs552656070	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946060	AGTATATACTCAAAG[G/T]ATTATAAATCATGCT	9873
rs552677918	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72995568	AATCAGCCAGGTGTG[A/G]TGGCAAGCACCTGTA	9873
rs552679966	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73030799	ATCCATCATTTCACA[C/T]TGTTATCCCTTTTTG	9873
rs552688952	in-del	-/TA	0.00037779	0.0137387	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843359	GTGACAAAACAAGTT[-/TA]CACACACAATTTAGA	9873
rs552689086	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72880404	TGTCACAAATACAGA[C/G]ACACAGACCAATGGA	9873
rs552698124	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72934354	TTTTTTTTTTGAGAC[A/G]GAGTCTTACTCTGTT	9873
rs552713783	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932020	CCTCTTAGACTGAAT[C/T]ATTCTCTTTTCCATC	9873
rs552717171	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72979110	TGATCTGCCCACCTC[A/G]GCCTCCCAAGGTGCT	9873
rs552726736	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927142	AAAAAACCCTGTAAG[C/T]CTTTAAGGGTAAGGA	9873
rs552728610	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72962941	GAAGGCACACTGGAG[C/T]CAGACTGGTTGAGTT	9873
rs552734470	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72952059	CTGAAGCTTCATGGT[A/G]GGTCTGCATATGTCT	9873
rs552740804	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72879023	GCTGAGGCAGGGGAA[A/C]TGCTTGAACCCAGGA	9873
rs552752243	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946694	ATGGTATAAACAGAG[C/T]AATAGCTACCATTTA	9873
rs552752346	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877034	TGCAGTGCAGTGGTA[C/T]GATCACGGCTCAGTG	9873
rs552756529	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986360	GACTACAGGCGCCTG[A/C]CACCACGCCCAGCTA	9873
rs552768830	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840568	ATTAAATGCTTACTG[A/C]AAAAAGTGTTTCACA	9873
rs552773883	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087798	TATACATTAGTTTCC[C/T]AGGCCTTTACATTCA	9873
rs552776834	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72951919	AAATCCTATTTGACA[A/G]GAATACTGTAACAGC	9873
rs552778655	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73096005	AACATCTAATATCCT[A/G]AAGTGCTATAGAAAA	9873
rs552781591	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73072912	AAATAGCAAAAAATT[C/T]TAGGTGCAACAGTAT	9873
rs552782931	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119270	ATCATGCCATTGCAT[A/T]CCAGCCTGCACAACA	9873
rs552799415	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72990458	ACATAGTTGGAAGTA[A/C]AGCACTCCTCAGCAA	9873
rs552813843	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927675	TTGCCACTGGCCTGG[C/G]ACCATACTTTGAAAA	9873
rs552821379	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848189	ATCTAAGGATCTTCC[A/T]AGCCAGGATAAAAAC	9873
rs552829078	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73079762	ATTAAAGAGTAAGAA[A/G]AACTCAGAAGGATCA	9873
rs552840851	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73133716	CAGAATTGCATGAAC[A/C]CAGGAGGCGGAGGTT	9873
rs552844877	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73073905	ATATCAGTTCCCCCT[A/C]AATTGACTTAAAGAT	9873
rs552862630	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72986645	TTCTCCTTTTTTTAC[A/G]GTCATTACCCAAATA	9873
rs552866030	snp	C/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73081995	ATCACCTAAGGTCAG[C/G]AGTTCGAGACCAGCC	9873
rs552876093	snp	C/T	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:73048082	AAGTTAAAAAAAAAA[C/T]ACAGGAGGAACAAGA	9873
rs552903485	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73088585	GTGTTTTAGTAAACA[C/T]ATAATGTTTGAAAAA	9873
rs552904458	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132900	ATATTTGCAAATCAT[A/G]TATGTTATAAAGAAC	9873
rs552910164	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73112304	TTGGCACTTTAAACA[C/T]GTCATGTCACTCTTT	9873
rs552924123	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73024822	AATCCCATTAAGAAA[C/T]GGGCAAAGGACATGA	9873
rs552925540	in-del	-/TTCT	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72901024	AAATTAGCATTTTTG[-/TTCT]TTTTTAAAAATTTAA	9873
rs552932020	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72872128	ATATACGTCTTTATA[C/T]AAGACAATTGGAATT	9873
rs552951628	snp	A/C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72957045	TTTCTTCTTTTTTTT[A/C/T]ATTATACTTTAAGTT	9873
rs552955200	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72948956	AGGCATGAGCCACAG[A/C]ACCCAGCATAATTTT	9873
rs552957965	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72917916	AAAAAAATTGAGGAC[C/T]GGCTTTTCCATTTCT	9873
rs552969922	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066655	ACAAGAAAAAAAAAA[A/C]CATCAAAAAGTAGGC	9873
rs552989438	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105377	TTCCACTGTCTACAG[C/T]ACACCCTCTATATAA	9873
rs552991370	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73096875	TCCTAGTTTTCTGAG[C/T]CTTTTTATCATGAAA	9873
rs552995729	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941868	AAGGAAGTTATCAAA[C/G]AGGTGTATTAAGATT	9873
rs553008216	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889256	GTGAGCCACCGCGCC[C/T]GGCTATAATTATGTC	9873
rs553015169	in-del	-/AAAC			intron-variant	FCHSD2	GRCh38.p7	11:72993067	AAATTTACAAGAAAA[-/AAAC]AAACAACCCCATCAA	9873
rs553039331	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949787	CTAGTTGATGGACAT[C/T]TGGGTTGTTTCCACC	9873
rs553041254	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72958121	TTCATTTCACATGAA[A/C]ACCTCAGCAATAAGT	9873
rs553050739	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73097688	TTCTATTTTTTTCTG[C/T]AATCAGTTTTAGTAA	9873
rs553052709	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73060287	ATTGAAGCATTATTC[A/G]TATCTTCATTTCTAC	9873
rs553060071	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72843763	AATCCTCAAGAGGCA[A/G]TGACGTTCAATGAAC	9873
rs553061287	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72884492	ATATATATATCTGTG[C/T]GTATGTTATATATAT	9873
rs553073926	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73106899	GAAATTACCTAATGA[C/T]GCATTTCTCAGAATA	9873
rs553076874	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72851361	TAGTGACAAACGCCT[C/T]GACACAATCTATATG	9873
rs553093577	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842534	GTAAGGCAGAGACTG[C/T]AGCCCACTTTTGTGT	9873
rs553096004	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881753	TGGAACTGGAGGTCA[C/T]TATGTTAAGTGAAAT	9873
rs553098045	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73118268	AGACTGCGGTGAGCC[A/G]AGACTGTGCCACTGC	9873
rs553104338	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73090947	CTTCTCCTCCCCTGT[C/T]AACTACTAATCTAAT	9873
rs553113296	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058740	ACCTGGCTAATTTTT[G/T]AATTTTTAGTCGAGA	9873
rs553115973	snp	A/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73093858	GATCTGCCCACCTCG[A/G]CCTCCCAAAGTGTTG	9873
rs553116041	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73057599	TTCTACCTCCTTCTA[C/G]GTGGCCATCAGGACT	9873
rs553139178	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035405	ACTCCTAAGCTCAAG[A/C]AATCCACCCACCTTT	9873
rs553142636	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73104613	TCGCTCTGTCACCCA[A/G]GCTGGAGTGCAGTAC	9873
rs553152401	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005229	TCTTTTATAGAAAAA[A/C]TCCTTGAAAGAATTG	9873
rs553159192	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980855	CTTCCCAAAGCCTAA[C/T]TCAGTAGTTAGCATG	9873
rs553167696	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73082890	TATACAACCATAAAA[A/T]GATACATCAACATAA	9873
rs553178414	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844446	AGCTGATCCATTTGC[A/G]TGCTACCGTACAAGC	9873
rs553179311	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73099343	TAGAACCCTCATGCA[C/T]TGCTGGTGAGAACAT	9873
rs553192291	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72996344	CTATAATGGATATGG[C/T]AGCAGTTTGCAAACT	9873
rs553198852	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099718	TGCACCCTCGGTCTG[G/T]TTGGGGCTGTCAAGC	9873
rs553213657	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997763	TGGAGTGCAGTGGCA[C/T]GATCTCGACTTCCTG	9873
rs553217623	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943090	TCCGCCTCCCGGGTT[C/G]AAGTGATTCTCCTTC	9873
rs553237440	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72866185	CAACAGTCTGAAGTA[A/G]ATGAGCATTATGACT	9873
rs553241964	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836716	AGGTCTGTTTACCCA[A/C]ACCTTTCTATATTAA	9873
rs553247110	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72981565	AATAGTAGACATATA[C/T]AGAATATAGTGAATT	9873
rs553255569	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73033140	AAAAATATAAAAAAT[C/T]AGCTGGGCATGGTGG	9873
rs553260250	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991247	CCAAAAACAGTCCAG[A/G]ACCAGATGGATTCAC	9873
rs553264153	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092549	TTAGTATTTATATGT[C/T]TGGCACAGTGACTGA	9873
rs553268346	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982735	CAGAGGACAGACATC[G/T]TCATATAGCTACTGA	9873
rs553277635	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73020392	TAAATTTTACTAAGG[G/T]TTTGCCATTAGATGG	9873
rs553293642	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875224	GGTAGATAATAGTAT[G/T]TGCTACTCCATCTTT	9873
rs553298311	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965233	CTGTACATTATACTG[C/T]AGAAATATTGAACTA	9873
rs553303785	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72930441	TAGAGATTCATCTCT[A/G]TATTTTCTTTGACTT	9873
rs553308765	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72987054	TCCAAACATATTCAC[A/C]CCAGTGTTTCCCAGG	9873
rs553317597	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73069534	ATGGATAAGATAAAA[C/T]CCTCAAATAGACACA	9873
rs553320727	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72912391	GCTTTTTCAGTATCA[A/G]TTGAAATGATCATAT	9873
rs553329952	snp	A/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73126183	CATCTCTACTAAAAA[A/T]ACAAAAATTAGCCAG	9873
rs553330081	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117406	TTCCATCCTATTAGG[C/T]TTTTAGGCATATTTT	9873
rs553340210	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091961	AATTGTTTGTACCGG[G/T]GAGACAGAGGTTGCA	9873
rs553368147	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858570	GAAGCTAAATGATTA[C/G]AACATGGACACATAG	9873
rs553383134	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72949156	ATTTTTATCACCACA[A/G]AAAGAAACCTGGCCG	9873
rs553389124	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73114326	GGACTAACCCTTCAG[C/T]GCAGTAGGCTCCCAT	9873
rs553402407	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084130	AATGTTGGCTACTGT[C/T]ATAAGAATAGCTACT	9873
rs553407327	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72942856	GTATGATCATAGTTC[A/G]CAGCTTCAAACTCTT	9873
rs553407536	in-del	-/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140781	TCCACTTCAAACAGC[-/G]GAGAACAGCAAATGC	9873
rs553414789	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059460	ACTTCAAAGAGTTCA[C/T]AAATCATAAACATAA	9873
rs553431131	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851222	AAAACAACCTGTTCA[A/C]TGAAATTAAAAACTA	9873
rs553435137	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029396	TGTGGACTTGCAACT[A/C]CCAGAGAAAGATTTG	9873
rs553455870	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73006084	GGCTATTTTTTTTTT[A/T]AAATAAAAATAGTAT	9873
rs553461272	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72968537	CATGTATCTTAATGG[A/G]GAGCCCTGAAGAGGA	9873
rs553464441	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847000	AATTTAAATTTTTTT[A/T]AAATTTATTTTTTAG	9873
rs553474931	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73102127	TGGTAACAGTGAAAA[G/T]ATGCTTAACATCACT	9873
rs553481779	in-del	-/ATA	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72908591	CTGAACTAGGATGAT[-/ATA]ATATCTTACTGTAGT	9873
rs553488428	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051600	CAACGACTTTATACT[A/G]TTTTACACAAAAGTA	9873
rs553504403	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73137082	GTGAATTTTTAAAAA[A/G]TCATTCCACTTACTA	9873
rs553515271	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998330	AGATCACTTGAGGTC[A/C]GGAGTTCAGGACCAG	9873
rs553515442	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73052506	CAGTGTATTAGAGAG[C/T]ACTCTCTTCACTGAG	9873
rs553515748	in-del	-/TGGGGTATAGAGCTTTTT	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72967638	CAAAATGACAGCCAA[-/TGGGGTATAGAGCTTTTT]TGGGGGATAACAGAA	9873
rs553522228	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898621	CATCCCACTTTCATC[A/C]TCAAGTCTACTTGCT	9873
rs553538137	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102766	TCCTCACCAGATGCT[A/G]GTGCCTTGATTTTGG	9873
rs553552240	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73064776	AATGGATAAATTCCT[C/T]GACACATACACCCTC	9873
rs553554192	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72943556	AGGGAAGGAAATTGA[A/G]GAGAATGACAGGTGA	9873
rs553570206	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890639	ATAGCTAACTTCTAT[C/T]GTGCAAGGTACTATG	9873
rs553576844	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73086739	TATAGAAGTAAAAAG[A/G]CTGTACAGAGTATTA	9873
rs553577016	in-del	-/AT	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73050378	GACGTATTTAGATTG[-/AT]ATAGAGACATATCAT	9873
rs553577068	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847850	GGCGCCCGCCACCAC[A/G]CCCAGCTAATTTTTG	9873
rs553577884	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062503	CTCCAAGCTAAAGGA[A/G]CATGTTCTAACCCAA	9873
rs553579402	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73091599	TTCCAGACAGAATTA[C/T]AGAATGTCAAACCAC	9873
rs553592776	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936463	TTGCCTGGGAATTAT[A/C]AGTGTGATTTTATCA	9873
rs553595364	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72994287	GTCTGAATGCTTATT[A/G]CTTCTAAAAAGACCC	9873
rs553599387	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73103645	AACTAAAATGAACCT[A/C]TGTAAAACCTACACA	9873
rs553606079	in-del	-/A/AAA	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72968090	GCAAGACTCTGTCTC[-/A/AAA]AAAAAAAAAAAAAAA	9873
rs553612932	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72948198	TTTTTAGTAGAGATG[C/G]GGTTTTGCCATGTTG	9873
rs553614222	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73107638	CTTCCTTCTACTCTC[A/G]AGTTCCATGAGTTCA	9873
rs553631233	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116848	GGCCCATATCTCTTT[C/T]TTTAGTTATGAACTC	9873
rs553636129	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72948697	TTGAGAGGCAGTCTC[A/G]CTCTGTCGCCCAGGC	9873
rs553640436	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054983	GGTAGTTTATAAAAA[C/G]AGGTTTAATGGACTG	9873
rs553646655	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73006770	CTTCCCTCATTAGAA[C/T]GTAGGCTCCATGCAG	9873
rs553669344	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986498	ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCCCAAT	9873
rs553677978	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72923880	GGAGGTGGAGGTTGC[A/G]GTAAGCCGAGTTTGT	9873
rs553682474	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137775	TAGAGTGCACAGTTA[C/G]ACAACCTGACGTCCC	9873
rs553684730	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73044304	AGTCAGAGGCTGAGT[A/G]TGGTGTCTTATATCT	9873
rs553685033	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036565	ATACTGCAAGTCCCT[C/G]ATAAATTATAATCAT	9873
rs553704556	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861767	AAACCCTATCTCTAC[C/T]AAAAAAATATAAAAT	9873
rs553709622	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72946246	TTCATGTCCTTTGTA[A/G]GGACATGGATGAAGC	9873
rs553711157	in-del	-/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72848692	TAACGCAGGGATGTG[-/C]CCTGGGATATGCCAA	9873
rs553719572	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72952776	TGTGCCAGGCACTTA[C/T]ACATATTTACAATTC	9873
rs553721111	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870985	ACTAACAGTAATGTC[A/T]TTGCTTTTAAACTAC	9873
rs553723946	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894949	ACTTTTCTAAAATCT[A/G]GAAAATTCTGAATTT	9873
rs553740176	in-del	-/ATC	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73085397	TAGGAGTCAACTGAA[-/ATC]AGAGAGGGGATGACC	9873
rs553740180	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928610	TAGCTCTTCCTTAGC[A/G]TTTTCACAATATTCT	9873
rs553747964	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73037386	ATCATTACAGTATCA[C/T]AGGGAGTTATTTTCA	9873
rs553751162	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72879962	CGAGATCGCGCCATC[A/G]CATTCCAGCCTGGGC	9873
rs553759669	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73020851	TTTTATTTAAATTAA[A/G]TATATATAAGAAATA	9873
rs553776653	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72892035	AAGATTGAAGATATA[C/T]TGAAAGATTAAGGCA	9873
rs553785647	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113538	CACGCCCAGCTAGTT[C/T]CTCTATTTTTAGTAG	9873
rs553790360	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009126	AAATGCTGCATGTAT[C/T]ATCAGATAGGCAAAC	9873
rs553814604	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72866142	CCAAATCAAGTGGGC[A/C]TGGAATTTGCTGTCA	9873
rs553821059	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72917308	TCTTTTGCATGTGGC[G/T]ATCCAGCTGTCCCAA	9873
rs553823253	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054370	CATTCCAACACGCAG[A/G]CAGGGGGCTAGAAAA	9873
rs553831218	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953210	GAGAAATGGTCTTGA[C/G]AAAGCATGACAAGCA	9873
rs553833981	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909138	CTGCCTTGGGCTCCC[A/G]TGATTCTCCTGCCTT	9873
rs553842453	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72961738	TGTCATTTTTGTTTA[C/T]AGTTAATCACATGTC	9873
rs553847569	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72855227	GCTGTGAGCTGAGAT[C/T]GTGCCATTGTACTCC	9873
rs553848617	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120178	CAACACGTGGGAATT[A/T]TGGGAATTCAGGATG	9873
rs553851737	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000837	AACATAGTACTTAAT[A/G]AGAACATGTTGAAAT	9873
rs553853057	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73088188	TTTTTTAATCTTTCA[A/T]ACCATATTTTTGTTG	9873
rs553870165	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945767	TCTCAAAAGAAGACA[C/T]TTATGCAGCCAAACG	9873
rs553876170	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72863013	CTGTAACCTTGAACT[C/T]CTGGGTTCAAGATAC	9873
rs553884637	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72893974	AAGGCATAGAAGGCT[C/T]AGATATCTGAGCAGA	9873
rs553896429	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73019599	CATGAAATAGACAAA[A/C]AATGAGATCTTTAGA	9873
rs553921920	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902213	TGATTTCTGTGGAGG[A/G]GTACAACATAAAAAA	9873
rs553939494	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019329	ATCACCACAGAGAAA[C/T]TGGACATTAAAAGCA	9873
rs553941149	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010656	CTTTGGCTATGAACA[A/G]TGTCAGTGGTGTTTG	9873
rs553962963	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902940	TTACACAAAAAGCTA[C/T]TCTGTGTAACACAGA	9873
rs553968688	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045669	AAACTATCGCAAGAA[C/T]AAAAAACCAAACACC	9873
rs553973672	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114009	GCTGGGCCTCTGTCC[C/T]TCCCTTTAGGGTGGC	9873
rs554030195	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046324	AAAGCCTTATGAACT[G/T]ATTTTAAAAAGAAAA	9873
rs554045325	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087512	GGAGTTTGAGACCAG[C/T]CTGCCAACATGGTGA	9873
rs554048231	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864126	TACAACAGAGTAGAC[C/T]GGCAGTTTGCCCTTG	9873
rs554061630	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72904749	GCCCCCACAGTGCAA[C/T]TGCACGATGCTGTTT	9873
rs554065078	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909914	GGAGCACCTCTGCCC[G/T]GCTGCCCATCATCTG	9873
rs554085555	snp	A/C	0.00199481	0.0315187	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142361	GGAGGAAGGTGGCGC[A/C]GCTCTCCCCGCTAGG	9873
rs554091199	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040058	ATGTTTCCTAAATAA[G/T]AGTTTCATATTATTT	9873
rs554098740	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73043688	CCAGCCTCCTTTAAA[A/G]TTAGATGTGACTATG	9873
rs554101731	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064175	ATTGAACAACCTGTT[C/T]CTAAATGACTACCGG	9873
rs554106361	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72882449	TTGGGGAATAGAAGC[A/G]AACAGTTAGATAGAT	9873
rs554110022	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856079	ACAAAGAATGGACAG[A/G]CAGGATTGGCCTTCA	9873
rs554130476	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111605	TCCATTTACATTCAA[C/T]GTTGTTACTGATAAA	9873
rs554153530	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73028839	TAGCACTTCCCCTTT[C/T]GTTCTCTCCGTCTCT	9873
rs554156415	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932356	TTGTGTATTTTACTT[C/G]ACTGCTCTACACTGT	9873
rs554161290	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057027	GGCGGAGCTTGCAGT[C/G]AGCCGAGATCACACC	9873
rs554180777	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73079095	TTATCAAACAGTGTA[C/T]TAAGGACTTGTCCAT	9873
rs554189781	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73003039	TAACTATGAAGACTG[C/T]ACAATAAAAAGACAA	9873
rs554192121	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883125	CAAAACAAAACAACA[A/G]CAAAAAAACCAAACA	9873
rs554192391	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875385	CTATTATTTATTTGA[A/C]AGAGTCTCGCTCTGC	9873
rs554193286	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932909	ATGAATAAACCTATA[C/T]TTGAGCCCCATGACT	9873
rs554214941	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72910086	CCCCATCTGGGAGGT[A/G]AGGAGCCCCTCTGCC	9873
rs554224529	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981847	TTAGCTGGGTATGGT[A/G]GCAGGCACCTGTGGT	9873
rs554234107	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73075602	GGACGGATCACTTGA[A/G]GTCAGGAGTTCGAGA	9873
rs554238596	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73087274	AAGATATAAAGAAAA[C/T]ATTTTTATACAGTTG	9873
rs554242305	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080167	ACGGGTATGGTGGCA[C/T]GCACCTGTAGTCCCA	9873
rs554246989	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927887	ACGCTCTACTTTAGA[C/T]GCAAGACAGGAATGA	9873
rs554271660	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73134826	AATATACTGTTTTCT[-/G]GGGGGGGAGTTTGTT	9873
rs554278555	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73027382	GAACTTTGAACTTGA[A/G]AGAGATGATTTAGGG	9873
rs554293617	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73108157	ATGCATTTCTCTGAT[C/G]ATCAATGATGTTGCA	9873
rs554310243	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73121428	GCCTCATAAAGCATT[A/G]TAAATATATAACTTT	9873
rs554311730	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081088	TCACTTTTCATAAAA[C/T]TTAATGTAGTATTTT	9873
rs554311797	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071433	GCAGTGGCTCACGCC[C/T]GTAATCCCAGCACCT	9873
rs554316996	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113403	AGACAAGGTCTCACT[C/T]TGTCACCTAGATTGG	9873
rs554325142	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73025977	GTTTTGACTAAAGAA[G/T]TATAGAGATTCATTT	9873
rs554332729	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72867319	AGAGTAGAAAAAGCC[A/C]TGGACTTGAAGTAAG	9873
rs554341708	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73110837	CTTCGTACTGCTGTC[A/G]TTGTATCTCATGGGT	9873
rs554342381	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73014642	CAACAGCTTGATTTC[A/G]TATTCAGACTCTAAA	9873
rs554362852	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135262	TACAGGGGAGAGTAC[A/T]GTAGTATGGAAATCA	9873
rs554371980	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907079	CCCTTGTAAGTTGGA[C/T]TCCTAGGTATTTTAT	9873
rs554372238	snp	A/C	0.0850919	0.187897	intron-variant	FCHSD2	GRCh38.p7	11:72913826	ACCAAAAAAAACCCA[A/C]AAAAAAAACAAAAAA	9873
rs554374634	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910350	AGCGACCATCGAGAA[C/T]GGGCCATGATGACGA	9873
rs554379072	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72962703	AGATGGTTAAACAAA[C/T]AGCTTTGTAATTTAA	9873
rs554380239	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112675	TGTTGTTGAGACGGT[C/G]TCTCGCTCTGTCGCC	9873
rs554382791	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864889	AGCTGCATGCAGGCT[C/T]CAGACACCTGCAACT	9873
rs554385457	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73072878	CAAGTCTTCATAATT[G/T]TATTTCTTAAAAGAG	9873
rs554388293	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73022986	AGAACAATTGAATGA[C/T]CATAAACAACAACAA	9873
rs554388603	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73056991	GGGAAACTGAGGCAG[A/G]AGAATGGCGTGAACC	9873
rs554403566	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73114901	TGAGGGAGGGGTGGC[-/A]CAAGTACTCCCTCGG	9873
rs554415957	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963600	ACCAGGGACCAGTTT[C/T]GTGGAAGATAATTTT	9873
rs554423637	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142013	GAAGCAAGACTTGCC[A/C]CGGAGGGAGCAGGCC	9873
rs554451821	in-del	-/AGCCTCCCAA			intron-variant	FCHSD2	GRCh38.p7	11:73053097	TGATCTGCCCACCTC[-/AGCCTCCCAA]AGCCTCCCAAAGTGC	9873
rs554459709	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72921120	GTAGCAGTTATGAAA[C/T]GCGTATTTTTAAAAA	9873
rs554496698	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052442	CCTGTCTAAACAGTA[C/T]GTTTAGTGACAATTA	9873
rs554503489	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144312	CAAGGTCAAGAGATC[A/G]AGGCCATCCTGGCTA	9873
rs554503723	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72955248	TAGTTTGCTATAGTG[A/G]GTCACAGAACCCAAG	9873
rs554520620	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860666	CGTGGGCAACATAGT[A/G]AGACCCCATCTCTAC	9873
rs554526642	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73104730	CGTGCCACCGCACCC[A/G]GCTAATTTTTGTATT	9873
rs554558189	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73052997	GATTACAGATGCCCG[C/T]CACCACACCTAGCTA	9873
rs554558413	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841074	TTGGGATACTGAGGC[A/G]GGAGGATTACTTGAG	9873
rs554560901	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036385	TTCACAACGTTATAT[C/T]GGTCTTTGGAGTCAA	9873
rs554565870	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72950858	CCTGGGCACATGCTG[C/T]GGGACTACACTTCCT	9873
rs554565894	snp	A/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73119614	ACCATACCTGGCTAA[A/T]TTTTTTTATTTTTTT	9873
rs554582326	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72899660	AAGGACTGCTCGAGC[C/T]CAGGAGGTTGAGGCG	9873
rs554595579	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982615	TCTTCTCTTTATTTC[A/G]GTGAAAGTTAAAGAC	9873
rs554602939	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937173	AAAGGCTTGATGAAG[A/G]AACTCTTAAGGCTTT	9873
rs554621742	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72875247	CATCTTTGGTACCTT[-/A]AAAAAAAAGCTCCAA	9873
rs554627256	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73127301	CCAAAAAGATCAAAT[A/G]GAATGTTAAAACAAA	9873
rs554630388	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974042	ACTGGGAAAAATGAC[C/T]AGCAGAGTTGATAAC	9873
rs554643529	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73083859	AAAGGACAATATTTT[A/G]TTCATCTTTATGTGC	9873
rs554645169	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008051	AAGACAACTCAGGAC[A/G]ATGTGATTAAGGGCT	9873
rs554654880	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72920165	AGACACAACACTGAG[A/G]AGCAGAATAAAGGTC	9873
rs554683129	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72947110	TGGTTTAACAGCTGC[A/T]TGCCCCATGGGGCCA	9873
rs554684669	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72929802	GTATTTAAAACACTA[C/T]ATTGAAACCATTTAT	9873
rs554685637	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952157	ACTTTAACTTATATT[G/T]GTCTTGCTTGGTCAC	9873
rs554722760	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944955	AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA	9873
rs554726294	snp	A/G	4.19992e-05	0.00458234	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867904	CACTGCAGGAGGGCG[A/G]GCCCATCGCTCATTT	9873
rs554727505	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930433	TTTTAATTTAGAGAT[G/T]CATCTCTATATTTTC	9873
rs554731523	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72931694	TGCTTGGACCCGGGA[A/G]GTGGAGGTTGCAGTG	9873
rs554740294	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72994192	AATGCTAGATGCTTC[C/T]CTACTGGCAAATTGT	9873
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	9873
rs554771205	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73052708	TCATCTTATATATTC[A/G]GTATTTTTAATAATC	9873
rs554772383	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075613	TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC	9873
rs554774469	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965956	GATACAATCTCAAAA[A/T]TATAAACATCGGCAG	9873
rs554784810	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076852	GCAGTGCCTCACGCC[G/T]GTAATCCCAACACTT	9873
rs554788262	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892893	ACAGGTGTGAGCCAC[C/T]GTGCGTGGCTGGTAA	9873
rs554799226	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72939916	AGCCACCATGCCTGG[C/T]CTTGACGGCTCTTTG	9873
rs554813415	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931038	TGTATCAAAACATCT[C/T]ATGTGCCTCACAAAT	9873
rs554815346	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72958290	TGGAAGGCTGAGGCA[A/G]GCGGATCACTTGAGG	9873
rs554826097	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967848	TGTAATCTCAGCACT[G/T]TGGGAGGCCGAGGCG	9873
rs554827121	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72878302	CTCTAAAAATAAGTA[A/G]AATCCCTCTAATTGT	9873
rs554840583	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73060394	TTGTATAATTTCATT[C/T]CAAACATTCTAATAC	9873
rs554855887	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851969	GCAGTGTCAACCTCC[C/T]GGGCTCAAGCAATCT	9873
rs554857121	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73090428	GACGGGGTTTCACCG[C/T]TTTAGCCGGGATGGT	9873
rs554885498	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951505	TAGCTCAATAAATGT[C/T]TGCTCTGGTGTTATT	9873
rs554902205	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959105	GAGACAAGCCACTTG[A/C]GATTCACAGGCTTAG	9873
rs554903394	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900396	TTAAGGCAAACAAGG[A/T]CACAACACCTAAGAA	9873
rs554918012	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73082286	AAGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC	9873
rs554926830	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72981286	GACCTACCCAATGCT[A/G]ATCAAATATATGCAT	9873
rs554935696	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73015440	AAGTATCAGTGAAGA[C/T]GGCAGAACATATACA	9873
rs554942283	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140213	ACATCTGTCAGAATA[C/T]GTCTCTTGCTCGCCT	9873
rs554945608	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72977222	CCACTACACCCAGCC[A/C]AAAACTATTAAAATA	9873
rs554967903	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73068445	TACAGTAAACCACCA[C/T]GGCACACAAAATTTA	9873
rs554967991	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923460	CCTTGCCAACACTTA[C/T]TCTTTTGTATTTTGG	9873
rs554971816	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72944289	TATAAACAGAACCAA[C/T]GACAAAAACCATATG	9873
rs554985167	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999062	GTCTGAATTCTAATA[A/C]CATCATTTGAACCCC	9873
rs554991313	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108518	CCTAATGTTTTCTTT[C/T]AGCAGTTTCATAGAT	9873
rs555000641	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940536	GGAGCTATGGAGAAA[C/G]AAGTAGTCTCATGTC	9873
rs555008867	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73065761	ATTCACAATCGCTAC[A/G]AAGATAATAAAATAC	9873
rs555052593	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100857	TTTTAGATGCTTCTA[C/T]GTGGGATTTTTTTTT	9873
rs555060784	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73125293	AGAAAACTAACATTA[C/T]ATTACGAGGTTTATA	9873
rs555085263	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142248	CGCGCTCCCGGTCGG[A/C]CGCCTGCGCCGCCGC	9873
rs555091405	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134382	GGCTGAGGTAGAAGG[A/T]TCACTTAAGTCTGAG	9873
rs555093798	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846149	TGTTTTCCCAGACTA[C/T]TCATGATGAGTAAGC	9873
rs555096855	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72848681	TCATAGTCTATTTAA[C/T]GCAGGGATGTGCCTG	9873
rs555104995	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895947	AAAGAGCCACCCATA[A/G]CAAAGAGAATTTTCA	9873
rs555105982	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72992024	ACCCCATCGTCTCAG[C/T]CCAAAATCTCCTTAA	9873
rs555109778	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044006	AAATAAATTTCTTTT[C/T]ATAAGCCTCAGTGAT	9873
rs555118712	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088968	AAGGAATAGCTTTTG[A/T]ACCCTTGATGTGCAT	9873
rs555121342	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73104662	CAACCTTCACCTCCC[A/G]GGTTCAAGCCATTCT	9873
rs555121955	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085697	AGACTACCTACAACA[C/T]TTAAAAACTTTTTAA	9873
rs555124371	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72884269	CAATCTAACAAACAC[A/G]TAAAGCCAGTATTGC	9873
rs555141767	in-del	-/A	0.319855	0.240042	intron-variant	FCHSD2	GRCh38.p7	11:73049875	ACAAAAGGACCATAA[-/A]AAAAAAATTGTTTTC	9873
rs555154787	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73141929	GTTAGCAAGGACCAG[A/G]AGGAGGAGGAGGGCC	9873
rs555184511	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73096781	TTCCCCAGCCTAGAC[C/T]GTGTCACTACACTCT	9873
rs555185906	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73090095	TGAATTATCAGTAAA[C/T]TGTGTTGGGATAACT	9873
rs555186143	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081260	CCACTATGGTGAAAC[C/T]CCAACTCTACTAAAA	9873
rs555207661	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869817	TCTAACCCATTTCCT[A/G]GACTTTTTCTCCTCT	9873
rs555211645	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72922444	GAAAAGTGACTCAGA[C/G]ATACTGCTTTGGGGA	9873
rs555219984	in-del	-/A	0.0952156	0.196321	intron-variant	FCHSD2	GRCh38.p7	11:72967200	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	9873
rs555223600	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73112857	TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTAG	9873
rs555224908	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971173	TAAGTAACTGGAACA[A/G]GTCAAAATATAAAAA	9873
rs555246879	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72985476	ACTTCATACACTTTA[A/G]TTCCTGCAAAGGTTA	9873
rs555251238	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877888	GCACATGTCTGTAGC[C/G]CCAGCTATTCGGGAA	9873
rs555269153	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72858327	GCACATGCATGTTCA[C/T]TGCAGCACTATTCAC	9873
rs555275588	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73023960	GGAAAGACCAATTGA[C/T]AGAGAAAACAGATCA	9873
rs555282918	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034409	GCAAAAACGTTCCTC[G/T]TCCTGAAAGAAGCAA	9873
rs555287938	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878542	TAAGGTGAACACTGT[C/G]ATAGCTTGTTTTACT	9873
rs555311297	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72963869	CCATGGACTGCTGAG[A/G]TCCAAGGCCCTGGGG	9873
rs555315584	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72971781	TAAGCAGAGAACCTG[G/T]CTAAGCCTACTTGGA	9873
rs555326549	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73017858	AAAATGTGAAAAGCG[C/T]CATTGCCTAGGTACT	9873
rs555341544	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72926143	AGTCCTGGGCAGAAG[A/T]GGGTGGGTTCCCAGT	9873
rs555381610	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002472	AACTTGCAATGTAAA[C/T]TCACCACAGGCTCTC	9873
rs555383091	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857126	GTTGATTTTTGGATT[C/T]CCATGGAAGGCAGTA	9873
rs555391633	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73096461	AAGGCTGAGGCAGGA[A/G]AATCACCTGAACACA	9873
rs555392168	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111496	CTATGTGTGTCTTTA[C/T]AGGTGAAGTGTGTTT	9873
rs555396927	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857778	TTATTGCAGAGGCAG[A/G]AAAGATGATCTTTTT	9873
rs555405013	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72999135	AAGCAGATACATTCC[C/T]TTCTTGGCTTAAAGC	9873
rs555439571	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072879	AAGTCTTCATAATTT[C/T]ATTTCTTAAAAGAGT	9873
rs555444484	snp	C/T	0.000400105	0.0141383	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841471	TTTGCTGAAGGAGAC[C/T]GGGGAAAGTACAGGG	9873
rs555453840	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72865229	TTCTGCTTCATGTTC[C/G]TCAGCCAGCTAGCTG	9873
rs555456978	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858477	TTGGAGGGACATGGA[C/T]AGAGCTGGAGGCCAT	9873
rs555460382	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72987509	ACCATATCCAATATA[A/G]AGTATTCAACAAACT	9873
rs555466998	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105446	TGGTAACATTACTTT[C/T]CTAGGGAAGAACTCC	9873
rs555505004	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73065232	AAATGTAATCTATCA[A/C]GTAAACAGAATCAAT	9873
rs555505279	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73019389	GTAACTAGTTAGGTG[C/T]GAGCTAGAATCCAAA	9873
rs555512999	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73098035	CCAACTTTAGTTTCA[C/T]TGATTCTCTTCATCA	9873
rs555520894	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997074	AGCAAGTCCAAAAAT[A/C]TGTATGCAATTTCCC	9873
rs555533636	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72889249	TACAGGCGTGAGCCA[C/T]CGCGCCCGGCTATAA	9873
rs555551111	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73138558	ATAAGTTAAAAAAAC[C/T]TTACATTTTTAACCA	9873
rs555552351	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72960787	ATAAAGAACCCCAGG[G/T]TGTGAAATACACTCT	9873
rs555561038	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880238	CAATTGCTATCAAAA[C/T]CAATGACATTCTTCA	9873
rs555561397	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72888649	TTGGAGACAGGGTCT[C/T]TCTCTGTCACCCAGT	9873
rs555568428	snp	G/T	0.021333	0.101051	intron-variant	FCHSD2	GRCh38.p7	11:73056439	TAAAAATTATTTTTT[G/T]TCTCCCTAGATTCTA	9873
rs555571840	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851137	AAAGGTTGCTAAGTG[A/C]TACCAAGGATGTGGA	9873
rs555573324	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73076786	TGTAATGTATTGATA[C/G]TACTAGAAGCTGGGT	9873
rs555590276	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73036778	TCAAGAAGTCTTCCT[C/T]CACAAATATTGTGTT	9873
rs555597220	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73004041	CTTGAACTGGAAGGC[A/G]GAGGTTGCAGTGAGC	9873
rs555601421	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035110	CAGGTTTAACTCCTG[A/G]ACCTTGACAAGTTAT	9873
rs555613182	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949221	TGGGAGGCCCATGGC[A/G]GGCAGATCACCTGAG	9873
rs555629366	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73136959	CTTGTACCCAGGAGG[C/T]GGAGGTTGCAGTAAG	9873
rs555651592	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73068827	GTAAAAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA	9873
rs555660055	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989942	AGGACTATTGTGCAA[C/G]GGTGAATAGTGTGGA	9873
rs555668392	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73000846	CTTAATGAGAACATG[-/T]TGAAATCAGAAAATC	9873
rs555671569	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72902467	CTTTTTCTGTCTGTC[A/T]ATGCCAAGGGTAACT	9873
rs555673502	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027605	GAAGAGAAATTCAAG[C/T]TGGCTGCAGAAATTT	9873
rs555678942	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72897665	ATAAACTGCTAGTTT[A/G]GACACCCAAACCCAT	9873
rs555683353	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881690	ACACAATGGAATACT[A/G]TTCAGTCATAAAAAA	9873
rs555704222	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72874271	AGCTCACTGCAGCCT[A/C]GAACTGCTGGGCTCA	9873
rs555710924	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129569	TCTCCCACCAACCCC[A/G]GATGGGACCGTCCAG	9873
rs555711610	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966936	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	9873
rs555713603	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976246	AGTATTTCTTGGGGA[A/C]TCTGTCCAAATACTT	9873
rs555714737	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72917849	GCTGAGCTCATGCCA[C/T]TGCACTCTAGCCTGG	9873
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	9873
rs555724944	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72892113	GGCAACTGATAGAGA[C/T]ATTTAATTTTTGTTA	9873
rs555732594	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72935285	TGTAATTTCCCCTAA[A/G]GTAAGAACTTTAAAC	9873
rs555733574	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73098605	AATTGATAGTCCAGG[A/G]AAAAAAAAACAAACA	9873
rs555750349	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967776	TGGTATGTGAATTAT[A/G]TCTAATTTTTTTTAA	9873
rs555769646	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73115310	TGGAAGAGGGGTGGC[A/G]TTGGCAATTCAAGAC	9873
rs555770234	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042813	TTTTACTTTTTTCTA[A/G]CTATTATAAATTTGA	9873
rs555771851	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73136801	TTGGGAGGCCGAGGC[A/G]GGTGGATCACTTGAG	9873
rs555783161	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72860755	CCTGGGAGGAGGAGG[C/T]TGCCGTCAGCTGAGA	9873
rs555789587	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73020258	ACACTAGGAAATGGA[C/T]TGATGGCTTAACCTT	9873
rs555791293	in-del	-/A	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73031029	ATACTATTCAGCCTT[-/A]AAAAAAAAGGGAGAT	9873
rs555795310	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861658	GGATAGGCCGGGCGC[G/T]CTGGCTCATGCCTGT	9873
rs555799181	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72976208	AGTATCTGCTCTAGT[A/G]ACTACTGGCATAAGA	9873
rs555802084	in-del	-/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72975963	ACAAAGAAAATATTT[-/C]ACAAGCTTCTAAAAA	9873
rs555813976	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72911863	TTTCATTTTAAGAGA[A/C]CTTTCACTTCTTTGG	9873
rs555818730	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73065889	ATATTCCATGCTTAC[A/G]GCTAGGAAGAATCAA	9873
rs555833081	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035921	AGACAGGGTTTCACC[A/T]TGTTGGCCAAGATGG	9873
rs555845895	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73013376	GTTTTCTTCTATGGC[C/T]CCAGTGCCCCTCTCC	9873
rs555853456	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72916361	GTCACCCAGGCTACA[C/G]TACAGTAGTAGCATG	9873
rs555855479	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877764	ATAATCTCAACACTT[A/T]GGAGGCTGAGGCATG	9873
rs555855927	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72972896	AACAATGCTGAAAGG[C/T]ACAATAAAAGGATTG	9873
rs555856751	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853736	ATAAATTGAACCTTA[A/T]CAAAATAAAAAATAT	9873
rs555858376	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008293	GCAGTGGGCCAAGAC[C/T]GTACCACTGCACTCC	9873
rs555860059	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73088613	AAAAAAGTCCTTTTT[A/T]AAAAAAATGCACATT	9873
rs555862220	snp	A/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72956929	CACTTCTTCATGTGA[A/T]ACATAGAGAAGACAC	9873
rs555868653	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108703	CCTCCCGAGTAGCTG[A/G]GACTACAGGCGCCCG	9873
rs555884322	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938677	GAGGGTCAATTTTCA[C/T]CATTCTTTTACTCGT	9873
rs555898022	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114515	AGTTTCTCACTGTAG[C/T]CACCATAGCTGGAAA	9873
rs555909277	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005007	TCCTATTACTTGCAC[A/G]AACTACCTGTGCTCT	9873
rs555917295	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73032044	TACACAATTATTAAA[A/G]AGAATGTGCTATATA	9873
rs555929156	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72869647	GTGATGCTGAAGTGA[A/G]CACATACTTGCATTT	9873
rs555930397	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109212	GCTATTCTGGGTCTT[C/T]TGTGGTTCCATATAT	9873
rs555946234	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949632	ATCATACAATATATA[C/T]GCTTTTGTGTCTGGC	9873
rs555957261	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73049294	AAAATTAAAACATGA[C/G]AGAAACTGTCTCATA	9873
rs555973174	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72854526	AGCTTTGAACTCCTG[A/G]ATGCAAGGGATCCTC	9873
rs555977069	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893205	GGGGGTTTTGCTATG[A/T]TGGCCAGGCTGGTCT	9873
rs555982518	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73069455	TATATACATACATAC[A/G]TATATACACACATCT	9873
rs556010446	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73050665	TCCATATCCACATGG[A/G]GAGATAATGGGAACA	9873
rs556017617	snp	C/T	0.00676609	0.0577691	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843653	GAAACATGTTGAACA[C/T]AAAAATTTAAATGCT	9873
rs556018354	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942062	TCAAAATCTCATGTC[A/G]AAATGTGATCTCCAA	9873
rs556022297	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73113649	GTATTTATTGTAGTC[A/G]TCATAGTCTGGGCTT	9873
rs556031439	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72893150	ATTACAGGGCATGTA[A/C]CACCATGCCCAGTTA	9873
rs556039979	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73099072	AAAAAATTAATTAGT[C/T]GGAGGTAGTGGTACA	9873
rs556042463	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72993653	CTCAGCAGACTATCG[A/C]AAGGACAAAAAACCA	9873
rs556049930	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72960725	TCTGCTTTGATAATG[C/T]TGGGAGTTGATGTGG	9873
rs556053624	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73084443	TTGCCTAGGCTTGAG[A/T]GCGGCGGTGAGGTCC	9873
rs556054959	snp	C/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72858801	ATGCTAAAAATATCA[C/G]GAAAATGGATTTGTG	9873
rs556055311	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942945	TCCCAAAGTGCTGGG[A/G]TTATAGGTGTGAGCC	9873
rs556061897	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009091	AAAAGTCTAATGCAA[A/T]TTGAGGTTTTAATGA	9873
rs556070649	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73007861	TACAGTTATGCAAGA[C/T]ATTACCACTGGGAGA	9873
rs556088546	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72953073	GTTATTGTGCTCCAA[C/T]AGAAAATAAAATAAA	9873
rs556105691	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869135	TGGTGTCGAACTCCT[A/G]ACCTCAGGTGATCCA	9873
rs556115407	in-del	-/AATG	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72884246	TTATACAACACAGTT[-/AATG]AATGGGTCAATCTAA	9873
rs556121411	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72902154	TGCTGAGATTACAAG[C/T]GTGAGCCACAGCGCA	9873
rs556132527	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72937878	CAGTTATTATGCTAG[A/G]CACCATGGGAAATAC	9873
rs556139353	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943501	AACAGTAAATGTGAA[C/T]TTCATATTACCTTGG	9873
rs556140271	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032146	ACATGTAAGCATATA[C/T]ACTCTAGAATACATA	9873
rs556141257	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72935597	GAAGACCCCAAGCTA[C/T]GCCTAATCAGGTTAC	9873
rs556179572	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73016110	GAGTTTGAGACCAGC[C/T]TGGCCAACATGGTGA	9873
rs556180687	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846820	ATAATTGAGCTCTTA[C/T]GGTACATACAATTTG	9873
rs556183038	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886582	TTTAATGGCTGGATG[A/G]TGTCAGTCTTTTATA	9873
rs556183669	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72935502	AGTTGTCTTAAAATT[A/C]AATCATGAAATTCTA	9873
rs556183871	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023911	CAAATTAAAAAGGTT[A/G]CACACTGTATTATTC	9873
rs556194744	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839243	CAAAAGAGAAGGCTA[G/T]AAAGGTAGGCTAGGG	9873
rs556200743	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73102635	AGATGATTAGGCCAT[C/G]AGGGCTCTGCCCTCA	9873
rs556211938	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72859397	ACCATATCACGGTGC[C/T]TGTGTTCAAGTAGCC	9873
rs556219303	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72905282	AAAAAGTTTTAACTT[C/T]TAATCTCTGTGGGTA	9873
rs556223311	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046144	TAAAGACACACACCA[C/T]GATGCCATGCTGATT	9873
rs556245422	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72972050	TTAATTGTACCTCAA[C/T]AAAATTGATTTAAAA	9873
rs556273261	in-del	-/TTTG			intron-variant	FCHSD2	GRCh38.p7	11:72892606	TGTGTTTTTGTTTGT[-/TTTG]TTTTTTGTTTTTTGA	9873
rs556279890	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137847	GCATGAAACGGTAGT[A/G]ACTAAGCCAGGAAAG	9873
rs556281855	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061289	AGATACTGTGCTTGT[C/T]GCATGGTTTTCGCAA	9873
rs556282348	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72888156	CTGAGAAACTGAATA[G/T]TTCATTGTGGGATGG	9873
rs556284610	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73039927	TAATATTCATGAGGA[C/T]ATCACAAAAGCAGTT	9873
rs556290235	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73046816	TTGAACTCCTGGCCA[A/G]AAACGATCCTCCTAC	9873
rs556322105	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73009764	CTGCTGAGAAATCTG[C/T]TAGTAGTCTCATAGC	9873
rs556323221	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901275	AGTGGTGCGTGCCTG[C/T]GGCCCCAGCTAATCG	9873
rs556335296	snp	C/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836342	GGCATCCAGAATGCC[C/G]GCTTCCTGGAAGCCA	9873
rs556337846	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932210	CCAACCCCTCCTCCT[A/G]ATCTCCACAGCTACT	9873
rs556344952	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73053398	TGAAAGATAGAAAAT[A/G]AATTCTGAAAAAAAT	9873
rs556355312	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73061712	GGAAGTTCGAACTGG[A/G]TGGAGCCCACTGCAG	9873
rs556364589	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73100441	CAATCTCGGTTCACC[A/G]CAACCTCCACCTCCT	9873
rs556366629	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978174	CATGGGGTGGGGGGA[A/G]CGGGGAGGGATAGCG	9873
rs556378271	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101987	CAGGGTAGGCCAGAA[A/G]CTGCAGACCCAGATA	9873
rs556381705	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73006763	TGTTTGTCTTCCCTC[A/G]TTAGAATGTAGGCTC	9873
rs556398636	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045532	CCAGATGTCCAACAA[C/T]GATAGAATGGATTAA	9873
rs556412342	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916359	CTGTCACCCAGGCTA[C/T]AGTACAGTAGTAGCA	9873
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	9873
rs556414063	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72945204	ACCAAAACAGAGATA[C/T]AGACCAATGGAACAG	9873
rs556427544	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143359	GAGGCAGGAGAGGCC[A/G]TAGAGGAAGCCCTTG	9873
rs556439493	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73094447	GAAAACGTGTCCACA[A/G]AAACACTTTTACAAA	9873
rs556444314	snp	C/G/T			intron-variant	FCHSD2	GRCh38.p7	11:73039724	CATTATCAAGGATAA[C/G/T]GAATGATGCAGGACT	9873
rs556446174	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909881	CTCTGCCCGGCAGCC[A/G]CCCCATCTGGGAAGT	9873
rs556453953	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73000221	ACACTGGATGGCTTC[C/T]AAAATATTATTTCCC	9873
rs556471418	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72870252	AAGCACTCTATATAG[A/T]TCTAATTACAATGTG	9873
rs556480640	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72985719	ATGATGTAATCTTCT[A/C]CCACTCTTGGGTTCT	9873
rs556490456	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73071594	TAGTCCCAACTACTC[A/G]GGGGGCTGAGGCAGG	9873
rs556497422	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72889294	AAATATGTCTTGAGG[A/G]ATGAAAACTTATATT	9873
rs556500228	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73136015	AATCTTTAAAATAAG[C/T]CAGGCATGGTGGCAC	9873
rs556528301	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938894	GTTTTTGAGTTGCAC[C/T]CTAAAGCTGATTTAA	9873
rs556539640	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931412	ATGCCCAGCCTTAAA[A/T]TTTTTTTTTAAATAA	9873
rs556540316	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73035189	GTATGTATGTATGTA[C/T]GTATGTATGTATGTA	9873
rs556579377	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086342	TGAACCCAGAGGTGG[A/G]GGTAGCAGTGAACCA	9873
rs556580983	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72889690	TGCCCTTCAACCTGG[G/T]TGACAGAGCAAGCCT	9873
rs556598276	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010626	GCTTGCAGTGGTACG[G/T]TATCTGTACGATTTC	9873
rs556611020	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954610	GAGTAATTCCAAGAA[C/T]ATAGTTGTCATTACT	9873
rs556614838	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129493	TATTGTGAACTGCAC[A/G]TGCAAGGGATCTAGG	9873
rs556615317	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939570	AAATTCTCTGGCTTA[C/T]AGGAAATCTATGAAG	9873
rs556628402	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120747	AAAATAATAATAATA[A/G]AACAAAAATTAAAAA	9873
rs556638237	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087412	TTTATTACTGAAGAA[A/G]GAAAAGTTTTTGGGC	9873
rs556642562	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72977404	GCAGAGACAGCCCAT[G/T]GAATGGTAAAAAATA	9873
rs556668263	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028747	CCTGGTGGGAGGAGA[G/T]TGGATCATGAGGGCA	9873
rs556680839	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73070580	AGGCGCCTGCCACCA[A/T]GTCTGGCTAATTTTT	9873
rs556709403	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017400	CGTAACTAAAAAGAA[C/T]ACAATGCTGAAATGA	9873
rs556726727	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72881866	AGAGGCTGGGGCCGG[A/G]TGCGGTGGCTCACGC	9873
rs556731400	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029246	TACGGAAACCACTTA[C/T]AAGACTATTGTAGGA	9873
rs556741002	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927304	TCTGTATGATACTAC[A/C]ATGGTGGATACATAT	9873
rs556759118	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73080105	GGAGTTCGAGACCAG[C/T]CTGGGCAACATAGTA	9873
rs556770556	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73010184	TTGATCTAGTCTATT[A/G]TTGAAGCTTTCAAAT	9873
rs556772498	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066218	AACCAACTGATCTTT[A/G]ACAAACCTGACACAA	9873
rs556789445	in-del	-/A	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73138549	TTTGCTTAATAAGTT[-/A]AAAAAAACCTTACAT	9873
rs556805983	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970273	TTAACCAACAATAAA[C/T]ATTACAGAATCTAAG	9873
rs556809238	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72919998	CAGTTCAAGCAGAAA[C/G]ACACTTTTTTAAAAG	9873
rs556815627	in-del	-/CTGATTATAAAATACATG	0.0573587	0.15934	intron-variant	FCHSD2	GRCh38.p7	11:72947753	TGAAAACATAATTTT[-/CTGATTATAAAATACATG]CTCATAAAGAAAATT	9873
rs556823954	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72903168	TACAGCATACCAAGA[A/C]GACAGGCTAGAAAGG	9873
rs556834130	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848038	CTCACCAGATTATTC[A/G]AGGCCTCCTTTTTGG	9873
rs556835437	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066804	TCTCACGCCAGTTAG[A/C]ATGGCGATCATTAAA	9873
rs556848974	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855420	GGCGGAGGTTGCAGT[A/G]AGCCAAGATCATGCC	9873
rs556851235	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074055	CAAGATTTATTGTTA[C/T]AAAGACAAAGTACTT	9873
rs556898982	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059620	GAAAAGCAAAATTAG[G/T]CTATGAAAATTCAAG	9873
rs556903565	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997521	AGAAAAACCGCAGGC[A/G]GTTAAAAGAGACCTA	9873
rs556906927	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73127161	CTCCAACTTGTTTCT[A/G]TGGAACCACAGACAT	9873
rs556916901	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965382	ATGCACTAAAACACA[A/G]TAGGAAACAATACAC	9873
rs556919977	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042770	GTTGTAGGTCTTTCA[C/T]CTCCTTGGTTAAATT	9873
rs556924298	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73110811	AGGTACTTATAGCTA[C/T]GAACTTCCCACTTCG	9873
rs556953889	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72957329	GAGAATGATGGTTTC[C/T]AGTTTCATCCATGTC	9873
rs556969208	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72935436	CGGGCATTTCTAAAA[C/T]AGACTTTGGTAAAAG	9873
rs556975204	snp	A/G	0.0240643	0.107019	intron-variant	FCHSD2	GRCh38.p7	11:73090351	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	9873
rs556977277	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73035846	CTGCCTCAGCCTCCC[A/G]AGTAGCTGAGACTAC	9873
rs556979079	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73098574	AGTTTGTTTACAGTA[C/T]GGTTAGTTGGAATAG	9873
rs556988228	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72906184	CTCTGATGACCAGTG[A/G]TGATGAGCATTTTTT	9873
rs556994723	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851381	CAATCTATATGTCCA[C/T]CAACAGGGGAATGTT	9873
rs556998221	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882244	TCAGGAGTTCGAGAC[C/T]AGCTTGGCCAACATG	9873
rs556998443	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963690	GGCATTAGATTCTCA[C/T]AGGGAGTGTGCAACT	9873
rs557027961	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951453	TCAACCTTGGCACTG[A/G]CTTATACGTAAAGCA	9873
rs557027988	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943601	GCACAGAAATGGAAG[C/T]GAGAATTCCCTGGGT	9873
rs557040792	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091210	GTATTATGGATAATG[A/C]TGCTATCCACATTCA	9873
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	9873
rs557064001	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72853635	GCCCAGGCTGGTCTC[A/G]AACTCCTGAGCTCAG	9873
rs557086635	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72875361	AACTCTATCTATCTA[G/T]CTAGCTAGCTATTAT	9873
rs557091776	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117625	GTGGTTTTGTTTGTT[C/T]TTAGTTTGCAAGCAC	9873
rs557100380	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73051672	GAGATGTACTGGCTA[C/T]GCAACAATAAAACCC	9873
rs557103636	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116806	CCTCTCAAAGTGCAC[A/G]GATTACAGGCATGAG	9873
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	9873
rs557108951	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73090952	CCTCCCCTGTCAACT[-/A]CTAATCTAATTTTTT	9873
rs557111516	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092805	ATCAAGGAGGGCATC[A/G]GAGTATACAGTAAAG	9873
rs557141819	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132763	CAGAAGGTGGAGATT[G/T]CAGTGAGCCATGACC	9873
rs557144908	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72972834	ATCACCAAGTGCCTA[A/T]CACCTAGTACAAACT	9873
rs557151442	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043835	TAGAGGATCCATTGA[A/G]GACTTGAGGCCCTAA	9873
rs557155966	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074899	CCTAGGCGACAGAGT[A/G]AGACCCTGTCCCAAG	9873
rs557166942	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115951	TGGGTACTACAGCAT[A/G]AGCAAGTTGATACAT	9873
rs557176293	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022266	AAGCCCTACTTAGTA[C/T]AATAAGGCAAGAAAA	9873
rs557182064	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72845212	GATCACTTGAGGCCA[A/G]CAGTTTGAGACCGGC	9873
rs557194577	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900291	AGAGCACTGACAGGG[G/T]AGAGCTCAATATCCA	9873
rs557198292	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72990776	GATCTAAAATTGACA[A/C]CCTAACATGACAAGG	9873
rs557205080	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72852461	CCAGCACTTTGGAAG[A/G]CTAAAGTGGGTGGTG	9873
rs557232816	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72973906	CAGAAGCCTATTTAT[C/T]ATCTGTCCCTTTACA	9873
rs557235777	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014663	AGACTCTAAACCATG[C/T]GCTTCAATACTAAGT	9873
rs557236139	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73085584	CAACCACATTTAAGG[A/G]AGAAATTGAAAAGTC	9873
rs557236950	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72867253	ATCAACCGAATTTTT[C/T]TGGTACTTAGATCTC	9873
rs557243350	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73060678	TAAAAAATAAAAAGG[-/A]AAAAAACTATAAGAC	9873
rs557245207	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143957	TAATCAAATCAGGGA[A/G]GGCCTGGGGCAAGGG	9873
rs557260895	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72977749	AAACTAGTTCAACCA[C/T]TGGGGCGATTCCTCA	9873
rs557262661	in-del	-/A	0.0209421	0.100162	intron-variant	FCHSD2	GRCh38.p7	11:73049684	AACTTAGAGTATAAT[-/A]AAAAAAAAAAAAAAA	9873
rs557290748	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958172	GGGAAAGATGGCTTG[A/C]TTTAAATCAAGTCAG	9873
rs557323089	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72906934	TTCCATATGAACTTT[A/G]AAGTAGTTTTTTCCA	9873
rs557335921	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038154	TTCAAGCCAAGCCTA[A/G]GCAACAAGGAGATCT	9873
rs557338750	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72910260	GCCTCTGCCCGGCCA[C/T]CCCATCTGGGAAGTG	9873
rs557372589	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73075899	CAACGCAGTCGGATC[A/G]CTTGAGTCCAGGAGT	9873
rs557380608	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73107567	GTTTATACCCATTAA[C/T]CATCCTCACTTCCCA	9873
rs557391974	in-del	-/TATT	0.0341408	0.126114	intron-variant	FCHSD2	GRCh38.p7	11:72914009	CATACTGCCTTAAGC[-/TATT]TATTTATTTATTTAT	9873
rs557394856	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023301	TCATGTATCTGATAA[A/G]GGAAGTCCAAATATA	9873
rs557410814	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930333	TCAAAACTTTACTAG[C/T]GCCAACCTTCTCTTT	9873
rs557412841	in-del	-/AGACT			intron-variant	FCHSD2	GRCh38.p7	11:72846143	CGCATATGTTTTCCC[-/AGACT]ACTCATGATGAGTAA	9873
rs557420634	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954441	AAACTCCTGGGCTCA[A/G]GCGATCCTTCCCCTT	9873
rs557423798	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844503	CTGACAGCAGCAATC[C/T]ACCAGCATCAGCCAC	9873
rs557432250	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006731	TGGCATATATGTTTA[A/T]TTATTCACTTGTTTA	9873
rs557446435	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099817	GAGTGCGAAGGGAAG[C/T]CAGGAGAGGCGGCAC	9873
rs557455660	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947047	GGCCCCAGGTGAGAT[C/T]CAGGTCCAAGAAAAT	9873
rs557458068	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72909452	AGCCTCTGCCCAGCC[A/G]CCACCCCATCTAGGA	9873
rs557468751	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044395	CCAGCCTGGGCAACA[C/G]AGTGAGGCCCTCTAT	9873
rs557470631	snp	C/G/T			intron-variant	FCHSD2	GRCh38.p7	11:72865871	TGCTACACAGTAGTC[C/G/T]AGTCATACACTGCCA	9873
rs557493393	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72991353	GGGAATCCTCCCTAA[C/T]TCATTTTATGAGGCC	9873
rs557504794	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855400	AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG	9873
rs557521446	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140472	TATTTCTAAAAAAGA[G/T]TCAAAGACATTAACC	9873
rs557525477	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110687	TGCTCCGATCTTTAT[A/T]ATTTCTTTTATTCTA	9873
rs557546958	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72937085	AAGAGGAGTTCTTCC[C/T]TAGCTGTGGTCCTGA	9873
rs557548505	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891704	TCAGATAGACTTAGT[C/T]TGAATCCATTGTATG	9873
rs557559673	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132391	TTCACACATACAAAA[C/T]ACTGAAGCTCAGAAA	9873
rs557575429	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096698	GTGTTCAGTCTTTCA[A/C]CACTGAGTACGATGT	9873
rs557580827	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983550	AATAAAAAATTCAGG[A/C]TAAGAGATACACTAT	9873
rs557586495	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104003	ATACTAATACAAAAA[C/T]ACAAATAAATGTTTT	9873
rs557590907	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72929660	TCTCAACATGGTTTG[C/T]GATTAGAAGGCAGAT	9873
rs557591358	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037439	TCTGCTATTTGTCCC[G/T]TCCCCTTCATCCTCA	9873
rs557595664	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72854510	GATCATAGCTCATTG[C/T]AGCTTTGAACTCCTG	9873
rs557597426	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72888127	AAGAAAACAAGATAG[C/G]CAAGTATAGGAATCT	9873
rs557608941	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047301	ATATCTGGTAGAAGC[C/T]ACATACCTAAATGAT	9873
rs557613540	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72957023	AGGACTCTAGTCTTT[-/T]TTTTTTTTTCTTCTT	9873
rs557615504	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72877004	TAGACAGGGTCTGGA[C/G]TTTGTTGTCTACGCT	9873
rs557621100	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140182	ATTTAACCCAAAAAA[A/C]TTGCTTCAGGAAAAT	9873
rs557628106	in-del	-/A	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72889546	AGACCCTATCTCTAC[-/A]AAAAAATCTAAAAAA	9873
rs557631885	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123315	TCCTAGCCAAGCCAG[C/T]ATTTCCTGGAATCCC	9873
rs557650650	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030399	TTTCACAACTGAATA[C/T]ACAAAACTCAATTTA	9873
rs557658681	in-del	-/CT			intron-variant	FCHSD2	GRCh38.p7	11:72885106	TAATTCCTTTGAAGA[-/CT]CTCATGGTCTAGTCC	9873
rs557668574	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73113239	TCGAATTTCTTAGAG[A/T]TTCCTCAAAATAGCT	9873
rs557683640	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970367	GAAAATTGTCTTTTA[A/T]CTAAAAGCCCTACAA	9873
rs557683699	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980084	GAGACTCTGGAAGAG[A/T]CTTCAACACAGATGA	9873
rs557684185	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940491	AGTAGCCATCAGGTA[A/G]GCCAAGATGGGTGCA	9873
rs557698165	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72872500	TACTTTCTGTCTATA[A/C]AGATTTGCCTATTCC	9873
rs557700115	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73054147	TGCTTACACTCTACA[A/G]CAGCAATGTTGGGAA	9873
rs557715470	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73093664	TGGAGTGCAATGACG[C/G]GGTCTTGGCTCACCA	9873
rs557719330	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932985	GTTAAAGGAGTAATT[A/G]ATTTCATAAAACTCT	9873
rs557737022	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73085966	GCAGATCTACTAAAC[A/T]AAGATACTAAAACAA	9873
rs557748468	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880059	CCCAAACCAAACCAA[A/G]ACAAGACAAAAACAA	9873
rs557754938	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73117500	ATTCATTAAGAGCTA[C/T]AAATTTCCTTTTGAA	9873
rs557767089	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73004457	CCTTTAGAATTCTGA[A/C]TCTAACAGTTACTCA	9873
rs557767380	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72966230	AGTGGTGCGATGTCG[A/G]CTCACTGCAACCTCT	9873
rs557767739	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971102	TGAAGGCAAACTAAA[C/T]GCTGTTGTTTTAAGC	9873
rs557775663	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72864204	TTGTGGGCTATAGTT[C/T]GAAAATGTAAGCAAT	9873
rs557785507	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73009998	AATAGATTTTTCTAA[C/T]CTTCCCTTCCCTCTT	9873
rs557788262	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72865052	TCCTTCCTTATTCTA[C/T]AAGGGAGTAGTCTGT	9873
rs557843444	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72957714	GTAATCTTGCATGGC[A/G]GATATAAATTCTGGA	9873
rs557845417	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011524	TTAGCCCTAGTGATG[C/G]TGGACCCCAGGACAG	9873
rs557846856	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010567	TTTCCTGAAGATAGA[A/T]CTATGGTGTTGTTTG	9873
rs557849726	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903736	CCATTAGCACCTCTG[A/C]TAGAAGATGGGCAGA	9873
rs557858278	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72994377	CTTGAAACGACTCTA[C/T]GAAAAAGGTAGTAGT	9873
rs557858658	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027565	GCAGCCTGACCATGA[C/G]GTAGAAAAGAAAAAC	9873
rs557860424	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72939872	GATCTGCCCACCTTG[A/G]CCTCCCAAGTGTTGG	9873
rs557888795	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886869	TCTAAACACTACACA[A/G]AATGTACATTTTTGT	9873
rs557896566	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123141	ATAAACAAGCCAAAC[C/T]GCCACTCTCTTTATC	9873
rs557906747	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73003116	GCAGATTTATAGCAG[C/G]GAAACATATCCTGAA	9873
rs557908623	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73012651	TCTTTTTCACAATAG[C/G]ACCACCATCCTCTCA	9873
rs557917166	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72917338	AAACCTTTTTCTGAA[A/G]AGAATATTCTTTCTC	9873
rs557942678	snp	G/T			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141515	AGGCTCTGCAAAGCT[G/T]CAGGGGCGTCCCCGC	9873
rs557947380	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963697	GATTCTCATAGGGAG[G/T]GTGCAACTTAGATTC	9873
rs557955088	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72954706	AGGCTGGTCAGGAGA[C/T]GAGTAGTGTACAAAG	9873
rs557962501	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72896896	CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCCC	9873
rs557962577	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857674	AGGCTGGTCTTGAAC[A/T]CGTGACCTCAGATGA	9873
rs557976694	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73099334	TGAAGAAATTAGAAC[C/T]CTCATGCATTGCTGG	9873
rs557983097	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72930641	TCCCAATTATTTGGG[A/G]GCCTGAGGCATAAGA	9873
rs557991810	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72990148	GCACTTAATAAGTGT[C/T]AGGCTGTGAAGGAAA	9873
rs558021425	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130120	ATCTCGTGATCCGCC[C/T]GCCTTGGCCTCCCAA	9873
rs558025248	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72887847	TAAGCTGAGACCATC[C/T]AATACTCAGATTAGT	9873
rs558026250	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72912146	CTCTTTCTTTCTTTT[A/G]TCTGACTGCTGTAGC	9873
rs558032326	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73033746	TCAACACTTGAGTTT[C/G]AGTACTGTACTGCCT	9873
rs558036622	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72955285	TTTTATTTATACTTA[C/T]TCATTTATTATAAAA	9873
rs558043171	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080278	ATCCAGTCTGGGTGA[C/T]AGAGCAAGACCCTGT	9873
rs558047144	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988041	ATAAACCGCGGAGCC[C/T]CTGAATTTTCACAAG	9873
rs558051946	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041415	TGTTCTTTTTAATAA[A/T]CACCATTCTGACTGA	9873
rs558064364	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73033542	AATGGAGGAATTATA[C/G]GGCGCTACACAAGAC	9873
rs558067009	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72904982	TTTATTTATTTATTT[A/T]CTTGGGAAGGTAACG	9873
rs558079954	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72965525	TTACATTTGTACATA[C/T]TGCCATTATAGTATT	9873
rs558085027	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983344	GGCATGGTAGCATGC[A/C]CCTGGATCCCAGCTA	9873
rs558095243	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876187	AATAAAATATTAGCT[A/G]GGTTTGGTGGTACAT	9873
rs558095989	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73063825	AAGAGACTTAGACTC[C/T]CACACAATAATAATG	9873
rs558098471	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72880869	TGATACCCTGTCTCG[A/G]AAAAAAAAAAAAGAA	9873
rs558099885	snp	C/T	1.66305e-05	0.00288357	intron-variant	FCHSD2	GRCh38.p7	11:72849734	CAGAATTTAATAACA[C/T]TATGTTGGAGAAATA	9873
rs558112889	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034381	TGATTTGACTTTGGT[A/G]GCACACAAACATGCA	9873
rs558122899	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72922230	TGCGTGGGTTCTGAT[C/T]TTTGCTCATCTGCTT	9873
rs558124282	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105420	CCCCAGAATCTACCA[A/G]GCTCTTTATTTGGTA	9873
rs558131730	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925250	TTTTTGACCTTACCA[A/T]AATCAGGATCATTTC	9873
rs558131993	snp	G/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72876965	TGTCTAACAGTAATA[G/T]GATCACTTCATTTTT	9873
rs558140383	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72881009	TTAAGGCCACAGGCA[A/G]CAAAACAAAAAACAG	9873
rs558144943	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73049274	CATAGTAAAACTTTA[A/C]GGAAAAAATTAAAAC	9873
rs558167408	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72996815	TGCCAGCATTAAAGA[A/C]CACCACCACACACTG	9873
rs558168291	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916482	CATGTCTGGCTAATT[A/T]AAAAAATTTTTTTGT	9873
rs558177096	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867955	GTTCATGGCACTCTT[C/T]AGCCATGTGTCCACA	9873
rs558191190	snp	A/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72868907	GTTACCTTTTTTTTT[A/T]AAATTTTTTATTTTT	9873
rs558205382	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72881864	GTAGAGGCTGGGGCC[A/G]GGTGCGGTGGCTCAC	9873
rs558231079	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072699	AAGATTGGCAGAAAG[A/G]AAAGCTCCAAATATA	9873
rs558232612	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72883807	CATGGTGGAGTGCGC[C/T]TGTATTCCCAGCTAC	9873
rs558234788	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73057259	TAAGTGACCGGCATA[A/G]TACCTAGGACACAGT	9873
rs558280662	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064255	AGAACAAAGACACAA[C/T]GTGCCAGAATCTCTG	9873
rs558294398	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72964536	AGGGCAAGGGCTGTG[G/T]TTTTGTTGCCTTTTC	9873
rs558296373	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73067182	AGTTCATGTCCTTTG[A/C]AGGGACATGGATGAA	9873
rs558301508	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119536	GTGGCACAATTATAG[A/C]TCACTATAACCTCAA	9873
rs558311681	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72992016	TTTAGAAAACCCCAT[C/T]GTCTCAGCCCAAAAT	9873
rs558327491	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911503	AAATTTTAGGATTGC[C/T]TTTTCTATCTCTGTG	9873
rs558328216	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73007381	ATCCCAGCATTTTGG[G/T]AGGCTGAGGCAGAAG	9873
rs558330130	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73015974	ACTTAGAAAATCTCA[C/T]TTTTCCAAATGTAAA	9873
rs558343715	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057075	GCGACAGAGCAAGAC[C/T]CCGACTCAAAAACTA	9873
rs558361211	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73119039	AGGCGCGGTGACTCA[C/T]GTCTGTAATCCTACC	9873
rs558364765	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905557	ACTCATCATTTACGT[C/T]AGGTATTTCTCCCAA	9873
rs558373929	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72988695	GATAAGCTTTCAAGT[A/C]TGTAAATACAATGTT	9873
rs558393956	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008223	GCACACCTGTAATCC[A/C]AGCTACTCAGGAGGC	9873
rs558425425	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126443	TGTGCTACAACCAAC[A/T]GGAAACCAATCACTT	9873
rs558426506	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73060646	CATCCCACTGAAAAC[A/G]CTTATGAATGAGAGA	9873
rs558444318	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901133	ATCGTGGCTCACGTC[C/T]GTAATGCCAGCACTT	9873
rs558449480	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72888515	AGGCAAAGAATGAGA[C/T]GGATATAGGTATCAA	9873
rs558453984	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73107970	TGGCAAGTGTATCTT[C/T]AGTTTTCTGAGTGAA	9873
rs558459271	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914252	ACTCCTGACCTAAAG[C/T]GATCTGCCCACCGTG	9873
rs558466117	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73045025	CAGTGAGCCGAGATC[A/G]CTCCACTGCACTCCA	9873
rs558479068	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892989	CTTTTTAAAATGCTG[A/G]CAAATTTATTTTTAT	9873
rs558486927	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72930784	TATTCAGACTGACAT[A/G]ATTTTTTAATTTTTA	9873
rs558496622	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72908537	CTCCACATCCTCACC[A/G]GCATCTGTGTTACTG	9873
rs558504717	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73097921	TCAAGCGATCCTCCT[A/G]CCTCGGCCTCCAACT	9873
rs558534324	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038510	ACAGCGTGGATACTA[C/T]GCAGCCATGAAAAGA	9873
rs558563726	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920390	TCCAGGAAAATGTAA[A/G]TTACCCAAATATACT	9873
rs558571052	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72853613	AGAGATGGGGTTTTA[C/T]CGTGTTGCCCAGGCT	9873
rs558572300	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72893679	TAGGCGTGGTGGCGC[C/T]GGAGGTTGCAGTGAG	9873
rs558578718	snp	A/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72930595	ACCAAAAATACAAAA[A/T]TTAGCTGGGCGTGGT	9873
rs558594086	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73039136	CGTGTATTCCAAATC[A/C]TATCTATTCCTAAGA	9873
rs558599129	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109117	TTTATGCCAGTACCA[C/T]GCTGTTTTGTAGTAT	9873
rs558602447	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966921	GTTAAGAAAGTGGCC[A/G]GGCGCGGTGGCTCAC	9873
rs558607596	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72993873	GTAACTAACCTGCAC[A/G]TTGTGCACATGTACC	9873
rs558618112	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075834	AAAATCATTAAACAC[A/G]GGGGCCAGGCATGGT	9873
rs558622902	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72913838	CCAAAAAAAAAACAA[A/C]AAAAAAAACCCTAGA	9873
rs558623543	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054015	AAAGGGGGGAAGAGT[C/T]CTCACAACAGATAGT	9873
rs558641437	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72860714	GCTGGGCGTGGTGGT[A/G]CTGGGAGGCTGAGGC	9873
rs558653893	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913146	GGGAACTCCATCCCC[A/G]TGATTTAATTACCTC	9873
rs558655428	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032024	TCATCAGTATGCTGC[A/G]ATGTTACACAATTAT	9873
rs558660572	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73065084	GGCCAATATCCCTGA[G/T]GAACATCAATGCGAA	9873
rs558665279	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931205	GTTCAAGTGATTCTC[C/T]TGGCTCAGCCTCCTG	9873
rs558666358	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000597	AATTATTATACAAAA[C/T]GGGTCAAGTTGAAAG	9873
rs558670908	in-del	-/TGT			intron-variant	FCHSD2	GRCh38.p7	11:73100332	AAGCGCTTTACATGC[-/TGT]TTTTGTTGTTGTTGT	9873
rs558677026	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73088036	AGGCACATGCCACCA[C/T]ATGTGGCTAATTATT	9873
rs558686937	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045360	TGGAAGTCAGTGTGG[C/T]GATTCCTCAGGGATC	9873
rs558698663	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73119472	TATGATGACAGATTT[A/G]TTTTTTAATACATAT	9873
rs558704725	snp	C/G	9.82946e-05	0.00700982	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141824	CGCGTACGCATCTCT[C/G]CGAACCCCAAAGCCC	9873
rs558706522	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907933	TAAACTATTGCTGAC[A/G]TGGTCACCTTATTGT	9873
rs558729368	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72993519	CAACCCAAATGTCCA[A/G]CAATGATAGACTGGA	9873
rs558732342	in-del	-/A	0.113334	0.209338	intron-variant	FCHSD2	GRCh38.p7	11:72983294	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAT	9873
rs558733522	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938789	TTCAGTTCTAAACTA[C/T]TGAAAAAAATCTTAT	9873
rs558744636	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73068121	TCCCACCAGGTCCCT[C/T]GCACAACACATGGGA	9873
rs558752961	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72959183	CAATCCTGGTTTCCC[C/T]GTTATTCTTTCTTTT	9873
rs558759741	in-del	-/AAC	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73030020	AAATGGCCAGTTTTT[-/AAC]AACAACAACAACAAC	9873
rs558762565	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73069841	CAAATAAAACATCTA[A/G]ATTCATAAATGATAC	9873
rs558765297	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73045883	GTAACTAACCTGCAC[A/G]ATGTGCACATGTACC	9873
rs558788656	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73050190	CAAATAGGTATGTCC[A/G]TGGTCTAACAAAACT	9873
rs558789170	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72924175	CAAACTTCTGGGTTC[C/T]AGTAATCCGCCTGTC	9873
rs558818983	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73070463	CAGTCTCGTTCTGTC[A/G]CCCAGGCTGGAGTGC	9873
rs558841621	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72944996	TAAATTATAGATTCA[A/G]TGCCATCCTCATCAA	9873
rs558872397	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72908533	TTTTCTCCACATCCT[C/T]ACCAGCATCTGTGTT	9873
rs558881527	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952223	CCAGAAAGATATATA[C/T]GGCCTATGAAGGAAA	9873
rs558896624	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72992114	GCATTCTTATACACC[A/T]ATAACAGACAAACAG	9873
rs558901959	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72846175	TAAGCTGCTCCTCCT[C/T]TTGCTCTTTTTTTTT	9873
rs558928869	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73060144	TGTATAAGGAGTTAG[C/T]CACCCAATAGATTCA	9873
rs558948624	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72933215	GGTGGAGGTGGTCCC[C/T]TGACTTAAATTAGGT	9873
rs558951503	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885375	TTGAGAATGTAGACT[C/T]AAATACTTGCATTAG	9873
rs558957367	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025462	CATGCACACATAGAG[G/T]GGAACAACAGGCACT	9873
rs558969458	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72880401	TATTGTCACAAATAC[A/G]GACACACAGACCAAT	9873
rs558970325	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72981613	CTGTGCTAAAAATCA[C/T]CTTTAGTAAATGTGT	9873
rs558973232	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925484	TGATCTATGATCGTG[C/T]CACTGCACCCCAGCC	9873
rs558973976	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73093519	AAGAGCTGTAATGCA[C/T]CCATTTAAATTCATC	9873
rs558975973	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101912	GTCTATGTATGAAAA[C/T]AGATTTGCTTTCAAG	9873
rs558988953	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878023	AAATATATAAAGCAA[A/C]TAAAATATTAGATAA	9873
rs558991287	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141357	CTATTCCAACTTCTT[C/T]TCGGCCGCCCCGTGG	9873
rs559006881	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72945646	TATTTTTGCAATCTA[C/T]TCATCTGACAAAGGG	9873
rs559015565	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086270	AAAAATTAGCTGGGC[A/G]TGGTGGTGCGTGCCT	9873
rs559019164	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72984469	CTTTGTAGATAACTT[A/T]AAAATATTTTGCCCA	9873
rs559021788	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73017335	ACTATAACAGGGCCT[A/G]ATGTAATGGTTATAG	9873
rs559029921	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73071650	AGGCTGCAGTGAGCC[A/G]AGATCATGTCACTGC	9873
rs559034253	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018705	TGAATAAAAACTTCT[C/G/T]TGGTTCCTAATTTTC	9873
rs559077590	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839062	GTTGTTCTCAATGAA[A/G]TATCAAGCCCACAAA	9873
rs559078359	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963319	TGGCAAAGTAGTGAG[C/T]ATTTACTACGCACTA	9873
rs559080403	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73092714	CAAGATCACAATCTA[C/G]ATCCACATGGACCAA	9873
rs559082008	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73077882	TCAAATTATAAATTG[A/T]GTGGCTTATTGTGTA	9873
rs559090808	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072317	CGAATAGCCATGAAA[A/C]AGTGAAACTTACTAG	9873
rs559107823	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73033787	TTAGTTATGAGTATT[C/T]TTGGATAAGACACCA	9873
rs559115604	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72979620	AATGAAAGAGTTTTC[A/C]ACCTTTAATTCTATA	9873
rs559117300	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72918331	TGTCATCTGCAAAGA[C/G]AGGTAATTTTAATTC	9873
rs559133725	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72986103	AGAGAAAACATTCAG[A/G]GATGAACACATATGC	9873
rs559148196	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977338	AATGGACAAATGGGA[C/T]CACATCAAGTTAAAA	9873
rs559156587	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064648	ATATCCTTATATCAG[C/T]GGTGATATCCTGTGG	9873
rs559166424	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73121817	ACATGGATTGCTGGG[C/G]TCCACTCTCAGAGTT	9873
rs559199319	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955586	GGATCCCTTGGCAAC[C/T]AGCCCCCATCCTGAC	9873
rs559219442	in-del	-/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72862934	TACATATATGATTAA[-/T]TTTTTTTTTAAAGAG	9873
rs559226570	in-del	-/AAC	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72852965	GGACACAAAGAGGGG[-/AAC]AACAGACACTGGGGC	9873
rs559237194	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978084	CCAAACACCACATGT[A/T]CTCACTCATAGGTGG	9873
rs559241386	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72870415	ATATCCTATATAACT[A/G]TGCTTCTACTTTTCC	9873
rs559243105	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72954865	CTCAATGTGAATTGA[C/T]ATCTATACATATACA	9873
rs559253461	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862534	TGACAAAGGATATGC[A/G]AGATCTATCTACTGA	9873
rs559259050	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72910141	AGGAGCACCTCTGCC[C/T]GGCTGCCCCATCTGG	9873
rs559284359	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72871123	ACCATAAACAAGTAA[A/C]CACAGAACTAGTTTT	9873
rs559286766	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72989597	GAACAAGAGAAGCAC[A/G]AAACCTGGGTACCAC	9873
rs559287439	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73128813	TATCTTTGAGATTAA[C/T]TTCACGTTTCAACCC	9873
rs559290845	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72978891	AGATGAAGTCTCACT[C/T]TGTCACCCAGGCTGG	9873
rs559308407	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72983963	CAATAACAAGTATAT[G/T]CCAATGAGATGCAAC	9873
rs559309566	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73140997	GGGTGAGTTAGGCGT[C/T]AGGCAAATGTTTGCC	9873
rs559312868	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117714	GTAAAGAATTTTACA[A/G]CTAACATCCATATAG	9873
rs559314663	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863104	GTTGAAATTTTTTTT[A/C/T]TTCTTTTTTTAGAGA	9873
rs559317989	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73105574	CTAAGCCTCAATTTT[C/T]ACATCTACAAAATAT	9873
rs559324258	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949360	GAGGCTGAGACAGGA[C/G]AATCACTTGAACCCT	9873
rs559331945	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72856429	ACTGTTTGCCTAATA[A/C]AATTCTATAGCACTG	9873
rs559347584	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73028001	AAACACCTGGATGTC[C/T]AGGCAGAAGTCTGCT	9873
rs559349562	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73089117	TTCACATAATAAATA[C/T]TTGGAAATCTATTCA	9873
rs559374414	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043259	TGAGAGATTTTATCA[C/T]GAAGGAATTTTTACT	9873
rs559380418	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098111	TTTCCTTTTGGGTTT[A/G]GCATGCTCTTTTCCT	9873
rs559381126	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987676	ACCCTATCAAATCCC[C/T]ACTTCTCAGAAACGC	9873
rs559383402	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034517	CTGAGCCTGTACCAA[C/G]GAAATAGAGATCAAA	9873
rs559400311	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131441	GGCTGAGGCAGGAGA[A/C]TGGCGTGAAACCAGA	9873
rs559418791	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843083	TTATCCTACTGAAGG[C/G]TTACTCCAGGGCAAT	9873
rs559422905	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72989361	CTGCTGATGACTGAC[A/G]TTAAGGTAAGACATG	9873
rs559425460	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73003341	TATGAAAATTCATGA[C/T]ACACAGATTCTTTTA	9873
rs559430022	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72880376	GACTTTAGTAACCAA[A/G]ACAGCATGGTATTGT	9873
rs559436457	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72975415	AAAATTACAGTCAGA[A/T]AGAAGGAATACATTC	9873
rs559441974	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73048634	TCTTACAGTAAGTGC[C/T]GGAAGTACGAAAAAG	9873
rs559444754	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73027693	GGGCATTTCAGAGAT[A/G]TTCGCTGCACTCCCC	9873
rs559451820	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72948582	TATCAATTTACATTA[C/T]CAATAATAGAATATG	9873
rs559454177	in-del	-/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72892616	TTGTTTTGTTTTTTG[-/T]TTTTTTGAGACAGAG	9873
rs559468163	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72909289	TGATCTGCCCGCCTC[A/G]GCCTCCTGAGGTGCT	9873
rs559468769	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72872898	TGGCTTTATCATTTG[A/G]TCCCACCAGTAGGGT	9873
rs559475396	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72917191	GGTTTCACCATATTG[C/G]CCAGGCTGGTCTTGA	9873
rs559477062	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72863096	CCTGGCTAGTTGAAA[-/T]TTTTTTTTTTCTTTT	9873
rs559486754	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72996301	TAATACTTAAATACT[A/G]TCAGGGTTGTGTAAA	9873
rs559490789	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941507	ACTTATTATTACTTT[A/G]TCATTAACTGTTTTG	9873
rs559510801	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990064	GTTAAGAAAGGACTA[A/C]AGGGGATGAGACATC	9873
rs559510810	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72981160	GTACAGTACATGAAA[A/G]CTGAAAGTATGTTTT	9873
rs559513005	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72845331	GAGGCTGAGGTGGGA[C/G]GATCACTTGAATCAG	9873
rs559517131	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889020	AGTGCAGTGGCGTGA[C/T]CTCAGCTCACTGCAA	9873
rs559523374	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850493	CGAGTAGCTGGGACT[A/G]CAGGTGCCCACCACC	9873
rs559538179	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018975	ATAACTCATTATCTG[C/T]AGAGAAGAATAACAA	9873
rs559546315	in-del	-/AAG	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73059383	AGGTTTTCTAGGATT[-/AAG]AAGTTGTAGGACGGG	9873
rs559562008	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72874901	AACTTGATGGCATTC[C/T]AGATACTACTTGACC	9873
rs559573440	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139423	GTGGTATTTCTTTCA[G/T]TAAAATAAGTCATCC	9873
rs559590856	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117096	TATTTTTGTTTTCCA[C/T]TCATCTTTCTACTTA	9873
rs559598772	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73019751	AGGTCCTAAATAATA[C/T]TGCACATTTCTGAAA	9873
rs559653304	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124337	ATGGGTGCAGCACAC[C/T]AATATGGCACATGTA	9873
rs559657264	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058004	CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGACTA	9873
rs559658569	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011773	GGGTCTCTCTTGGCT[C/G]CTGACTAATCCCACC	9873
rs559690928	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959988	AGGAAGAAACCTACA[C/T]ACTTCAAACACATAT	9873
rs559693369	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73081872	GGATTCAATAAATGT[A/C]AGCTATCATTACTAG	9873
rs559695752	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004192	ACATGGTAAGTACTA[C/T]GTTATGTATTTTACA	9873
rs559696351	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028275	CTTAAGGCCTTGGGA[A/G]CCCACATCTTGCAAC	9873
rs559697641	in-del	-/AAAATAAAAT	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:73080960	CTCAAAAAAACAACA[-/AAAATAAAAT]AAAATAAAATAAAAT	9873
rs559709560	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935796	TCAGGTTACTTCATG[A/T]TCTGTGAAAGAGGAA	9873
rs559714644	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73049467	GAAAGACTGGGAATG[A/G]GATGTAGACTACTAG	9873
rs559716011	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73100254	CTTCCTCCCTTCTCA[A/G]GAAAACCCTTCTCCT	9873
rs559721202	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73012932	ACAACTTGATTTCTG[C/T]TACAATTTCCTTGGT	9873
rs559737261	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882578	ATAAATGTCTGAGGT[C/G]ATAGATATCTTAATT	9873
rs559737476	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73129027	CAGGCATGTGCCACC[A/G]TGCCTGGCTAATTTT	9873
rs559756589	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854025	CACAATGAGATACCA[C/T]TTCACACCCATTAGG	9873
rs559756707	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72845770	TTCCCTCTTTCCTAT[A/C]TGATGAGCAGACTTA	9873
rs559756810	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72906476	TGCCATTGCTTTCGG[C/T]GTTTTAGTCATGAAG	9873
rs559757743	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72918395	TTCTTACCGAATTGC[C/T]CTGTCTAGGACTTCC	9873
rs559768272	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846347	CACCATGCCTGGCTA[A/C]TTTTTTGTATTTTTA	9873
rs559771047	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905660	GTTCTCATTGTTCAA[C/T]TCCCATCTATGAGTG	9873
rs559774641	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72991682	TTATCTCAATAGATG[C/T]AGAAAAGGCCTTTGA	9873
rs559792850	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73109699	GCTCTTTCTTTCTCT[C/T]GTCTGACTGCTCTTG	9873
rs559815778	snp	A/C	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72889463	CACTGCTGAGTGTTG[A/C]GAAAGTACAGAAAAA	9873
rs559827873	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72944584	GAAATAAAGAGTATT[C/T]AATTAGGAAAAGAGG	9873
rs559866459	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73042240	GAGATTATTTTTAAA[C/T]TCTGGTGAAAGACAG	9873
rs559879763	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091471	GGAGAATCACTTGAA[A/C]CCGGGAGGCAGAGGT	9873
rs559884681	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73117309	GAAGTGGAGAACTAA[A/G]AATTCACAATCAGGC	9873
rs559887012	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008395	TAATTTATATAATAA[C/T]TAGTAACAAGAAGAA	9873
rs559898467	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72993833	TTACTGGGTGCAGCA[C/T]ACCAACATGGCACTG	9873
rs559903312	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952565	CCTGACCTCAAGTGA[C/T]CTACCGGCCTCGGCC	9873
rs559906939	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72984915	CAAAACCCCCATGAA[C/T]TGGGAGGGAAAGTTC	9873
rs559907706	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941059	GCTATTGGTGGTTCT[C/T]GCCGGGCAGCTTAGA	9873
rs559930173	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042987	CTATATATGAGGTCA[C/T]GTCATCTGCAAAGAA	9873
rs559940860	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083172	AATACTTTACAAATA[C/T]AGTAAATAATGTCTC	9873
rs559945689	snp	A/C	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72986038	AGCAGTTAGTCTTTG[A/C]AAAGCCAGTGTGAAG	9873
rs559946068	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72867495	GTGCAAATCTCTGGA[C/T]GTTTATTTTCATTTT	9873
rs559952060	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000208	AATTAGAATCAAAAC[A/G]CTGGATGGCTTCTAA	9873
rs559953086	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72879911	GACTGAGGCCGAACA[A/G]TCGGTTGAACCCAGG	9873
rs559958964	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73054754	AATCATGGCTCACTG[A/C]AGCCTTGACCTCCTG	9873
rs559963437	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73028848	CCCTTTCGTTCTCTC[C/T]GTCTCTCCTGCCACC	9873
rs559973588	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73123227	CTGACATTTTTGACC[C/T]ATGACAAATTCAATG	9873
rs559988151	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870066	CCATCATGTGCTTGC[A/G]TGCCTGTGTGCGTGC	9873
rs559988585	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945407	ATTAATTCAAGATGG[A/G]TTAAAGACTTAAATG	9873
rs559993622	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035959	CTCTTGACCTTGTGA[C/T]CCGCCTACCTCAGCC	9873
rs560004633	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72893295	AGCATGAGCCTCCAC[A/G]CCTGGCCTAGATCAT	9873
rs560009035	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72903535	GGAATTTCTATAAAA[C/G]GAGAATTCTGATAAG	9873
rs560009367	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72973310	AGGCAGAGGTTGTGG[C/T]GAGACGAGATCGTGC	9873
rs560012099	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927415	ATGGTGTCAGTGTAG[C/G]TTCATCAATTGCAAC	9873
rs560023098	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021620	GGTACTAGGCTTAAT[A/C]CCTGGGTAACGAAAT	9873
rs560024145	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73088205	CCATATTTTTGTTGT[A/G]TCTTTCCTACATTTA	9873
rs560035104	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73135558	GTATGTAGAAACTTA[C/T]TGTAAGTGGTCTTAA	9873
rs560042934	snp	C/T	0.0193772	0.0965046	intron-variant	FCHSD2	GRCh38.p7	11:72896581	CTGCCAAGAAGGCCG[C/T]TGATGAGATCCTCTT	9873
rs560060676	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025046	CACTGTTTATGGAAG[C/T]GTAAATTAGCTCAGG	9873
rs560073516	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73094521	AGTTGTCCATCAATG[A/G]GATCATGGATAAACA	9873
rs560081132	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72967127	ATGGCGTGAACCCGG[A/G]AGGCAGAGCTTGCAG	9873
rs560086430	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73085608	AAAAGTCACCACACA[A/G]ACCCACGGGAAGGTG	9873
rs560086840	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73035233	GGTCTCGCTCTGTCA[C/T]CCAGGTTGGAGCGCA	9873
rs560088509	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73001592	TACTGAGATACAAGA[C/T]GAAGATTGGGTACCT	9873
rs560089565	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72999383	GGAGGGCAGTGGCAC[G/T]ATCTCAGCTCACTGC	9873
rs560100346	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143026	GCGCGAGAGAGGCGA[A/G]CAAGGACAAGTCGCT	9873
rs560101000	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870672	TTGGGAAGCCGAGGG[A/G]GGCAGATCACGAGGT	9873
rs560101355	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074277	TTTCAGTTGAGGAAG[A/C]ACAAAATATGCTTGC	9873
rs560110869	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72933042	GTAGTGGCATCCTTT[C/T]ATGTGGAATTCCAAG	9873
rs560120347	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892508	GCCCAGGCTATTAAA[C/T]AATACACAGAGAAAT	9873
rs560124503	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73112518	GCTTCTTATACTTGA[A/C]TACTGATAGCTTTCC	9873
rs560126005	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73062506	CAAGCTAAAGGAGCA[C/T]GTTCTAACCCAATGC	9873
rs560158842	snp	A/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73052717	ATATTCGGTATTTTT[A/T]ATAATCTTCATACTT	9873
rs560169547	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032356	ACCTCGGCTTCCCAA[G/T]AAACTAATATTACAG	9873
rs560176571	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909233	GTGGAGACGGGGTTT[C/T]GCCCTGTTGACCGGG	9873
rs560208078	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72884501	TCTGTGTGTATGTTA[C/T]ATATATCATATATAT	9873
rs560210523	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72865121	AGTTGCACTATTAAT[G/T]TCTAACAGTAGTATT	9873
rs560216114	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72901288	TGTGGCCCCAGCTAA[C/T]CGGGAGGCTGATGTG	9873
rs560218397	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093753	ATTACAGGCATGCAC[A/C]ACCATGCCGAGCTAA	9873
rs560222069	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73044759	AACATTCTAGCATGT[C/T]ATATAAAAATCATCT	9873
rs560223559	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72995831	CCTGGGCCAACACAT[C/T]GAAGTCCTACAAATG	9873
rs560252742	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73007573	GCCACTTCACTCCAG[C/T]TTGGGTGCAAAAGTG	9873
rs560264936	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915607	GTGGATCACCTGAGG[C/T]CAGGAGTTCAAAACC	9873
rs560276943	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73107034	TTTTTTGTTAGAAAA[G/T]CTATATATATATATA	9873
rs560281769	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73086045	AGAAAACTATGTGCG[A/G]GCAAAATGTAAATAT	9873
rs560284450	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045147	GAAGACATTTATGCA[A/G]CCAAAAAACACATGA	9873
rs560301779	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903310	CAAGCTCCGCCTCCC[A/G]GGTTCATGCCATTCT	9873
rs560305262	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72888994	CAGAGTCTCGCTGTC[A/G]CCCAGGTTGGAGTGC	9873
rs560315460	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112149	CTGATTAAAGAACTC[C/T]CTTTAGCATTTCTTA	9873
rs560324591	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976700	GTACTGGCATAAAAA[C/T]AGACTCACAGACCAA	9873
rs560327115	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938110	GGCAGAATTTAGTTA[A/C]CTGAGGTAAATAAAT	9873
rs560332442	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046775	TTGATTAAGACAGGG[A/G]TTTCACCATGTTGCC	9873
rs560334038	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862866	TGCAATACCGGCATC[A/C]AGCTGGACAAACAGA	9873
rs560335201	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886108	GGGTGTTAGAAAACC[A/G]TTAGTTTAGTTTAAA	9873
rs560344203	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854943	AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGT	9873
rs560346601	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72923037	TCATATAAATCAAAT[A/C]ATATAATATATGACT	9873
rs560355657	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72932507	CGTATTACACCTTCT[C/G]TACAATGCAGTTTTT	9873
rs560374168	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72979249	AAACAGAACTCTCAT[A/G]CATTAAAACTACTAT	9873
rs560376787	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119194	GTAGTCCCAGCTACT[C/T]GGGAGACTGAAGAGG	9873
rs560377115	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062664	TTTCAATAGCCAAAT[C/T]GATCAAGAGGAAGAA	9873
rs560413081	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72869708	AATATAACTTGTGAA[A/G]AGGAAGAGATCAAGA	9873
rs560413103	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930808	ATTTTTAAAGGGTAG[C/T]AGGGGTTGAGGAGGA	9873
rs560414374	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72968070	CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCT	9873
rs560414917	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72969739	CAGAAATTATAAAGC[C/T]ATGTCTGAAAATAGA	9873
rs560415930	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72963113	TTAGATCAGTGCCTA[A/G]CATATACTCAGTACT	9873
rs560432308	snp	C/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72870009	TTCTTTCCACACCCC[C/G]CTATGCTCCCACCCC	9873
rs560433670	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73077387	CATCTATCACAATAT[C/T]AAAAATTAAGAAGAC	9873
rs560434676	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914766	TTAAATGTAAAACCC[A/G]AAACTATAAAAACCC	9873
rs560438182	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055312	CACCCCACTGGACTC[C/T]AGCCTGGGCAACAGA	9873
rs560449733	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931544	GGCCAAGGCAGGTGG[A/T]TCACAAGGTCAGGAG	9873
rs560467603	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73078287	AAAACTGGCTGTATC[C/T]ACTAAAGTAGAACAT	9873
rs560472705	snp	C/T			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836626	GGATTAATTTACTTT[C/T]TCCTCTCTCTGTCTG	9873
rs560483366	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73070156	CAAAGATGTTCCTAG[A/C]CTTCATATAATGGTC	9873
rs560499436	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72894828	TTTCATATATACATA[A/T]ATGAATGAAAATATT	9873
rs560505551	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73112752	CTCCCAAGTTCAAGC[A/G]ATTCTCCTGCCTCAG	9873
rs560512458	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961198	AATCCAGGTGTTTCT[A/C]GGTCATTTTGAATTG	9873
rs560518729	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73002058	AGATTATAATATTCA[C/T]CTCCTGAGATTTCCC	9873
rs560544711	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73025680	ATAGAATTTTAAAAA[A/T]TTTTTAAATCTCCTT	9873
rs560546086	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953480	AATTTACAGCTATAT[A/G]AAAGATACTGCTAAT	9873
rs560547166	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962026	ATTGAAACCTAAGAA[C/T]TCCATTGAAATATTC	9873
rs560552838	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895402	CAAAAATGGCATAAA[A/T]ACCTTGCGTCTAACA	9873
rs560557945	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73020639	TTTAAAATATTCTTC[A/G]TTGTTCTGTGTGGTA	9873
rs560558127	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72956026	TAGTTGATTCCAGAA[C/T]TGGGGCAAAGAAAGT	9873
rs560562232	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73002690	TCTCTCAGTGTAACA[A/C]CCTCTTCTCTTTATC	9873
rs560566532	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062206	AACTTCAGCAGACCT[G/T]CAGCAGAGGGGCCTG	9873
rs560592321	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847492	AACTTCTCCCTTCAT[A/G]GACCTTTAGCGGGGA	9873
rs560596203	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863474	TACCACACCAAAAAT[A/G]TGATCCATAAAAGAA	9873
rs560611476	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72940045	AGTGTTACAGCCTGT[A/G]TAGAAAATGCAAGCA	9873
rs560617999	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911899	TCCTATGTATTTTAA[C/T]GTATTTGTAGCTATT	9873
rs560621840	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73126787	TCACGTCTGTAATCC[C/G]AGCACTTTGGGAGGC	9873
rs560624496	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73037850	CAAACATAGTGGACA[A/G]CTTTAGGAAAAGAAG	9873
rs560641392	in-del	-/T	0.26326	0.249648	intron-variant	FCHSD2	GRCh38.p7	11:73100863	TGCTTCTACGTGGGA[-/T]TTTTTTTTTTTTTCC	9873
rs560652970	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72912683	CTATTTTTTGGAATT[A/G]GTTGAGTAAAATTGG	9873
rs560654777	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905789	CTTTTTATGGCTGCA[G/T]AGTATTCCATGGTGT	9873
rs560659458	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72855594	ATATTTTACCATACA[C/T]ACGAACAAACGTGAA	9873
rs560672684	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73127631	CCATCAACTTACAGG[C/G]CTCCTCAGATAAACA	9873
rs560674816	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73121178	ACACATACACATACA[C/T]ACACACACACACACG	9873
rs560684304	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73066776	TGCAAATCAAAACCA[A/C]AATGAGATATTATCT	9873
rs560686309	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125897	CAAACCATTCTTCCA[C/T]GGAGAGAGCTGGCTA	9873
rs560693556	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142152	GAAGGAGGCGGAGAC[A/G]GCGAGGGGGCGGGGG	9873
rs560700574	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72946045	GCCATTCCATTACCG[A/G]GTATATACTCAAAGG	9873
rs560702953	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72848240	CCAAGGCCCTTTACT[A/G]TCTGACAACAAACAC	9873
rs560721700	in-del	-/TTTGGGTTGGG	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73127842	CTGTAATCCCAACAC[-/TTTGGGTTGGG]GGGCGGGGGTGGGAA	9873
rs560727350	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72994503	GCAAGGATGTGATGA[C/T]ACCATTTACTATGGA	9873
rs560733171	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72943011	GACTTTTTCTTTTGA[A/G]ACAGAGTTTTGCTCT	9873
rs560739399	snp	C/T			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144088	CAATTTATTGTGAAG[C/T]GTTGAGCTAGTCAAT	9873
rs560747602	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134048	ATCATATATGATATA[C/G]AGTCACATCATGTAA	9873
rs560767483	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056343	CAAATTGCTAATTGA[G/T]GTACAGGAGTTATTT	9873
rs560770261	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986855	CAAACACTACACAAA[C/T]AATGAACTATACCGC	9873
rs560777228	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051140	GGGCTAACAAAGTGA[A/G]ACCCTGTCTCTACCA	9873
rs560782632	snp	A/G	1.7894e-05	0.0029911	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840990	AAAGAAGCTCATTTT[A/G]CTTGAGTTGTTGAGC	9873
rs560790418	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73013096	TCAACACCTCCATTA[C/T]GTTCTGAATAAAAAA	9873
rs560792460	in-del	-/AAAC	0.00159617	0.0282053	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837231	GTTAAGAAGTGTAAA[-/AAAC]AACAACGAAAAAAAA	9873
rs560795871	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73095916	GCTGAGGATTAAAAA[A/C]AAAAAAAGTTATGCA	9873
rs560838602	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947253	AAACTTCCCCTGGGT[A/G]AGAAATGCTGTGTGT	9873
rs560841195	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73051747	AAACAACAAAAAAAA[A/T]TTGAAATAAATAGTA	9873
rs560845342	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043217	CCTTTATTTTGCTGA[C/G]GTATGTTCTTTCTAT	9873
rs560857746	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73020235	CAAAGAGAGCCACTG[C/T]TGAGTAGACACTAGG	9873
rs560859392	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087736	TTTTTAAAATAAATT[G/T]AGTGCAGCCTAAGTG	9873
rs560883549	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033243	CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA	9873
rs560900003	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72972003	CAAAACTCAACCAAC[A/C]CTATTTTAAAATAGA	9873
rs560901784	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72874684	AAGATTTTGTCAGTA[A/T]TTTATCAAACAACAG	9873
rs560907900	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074141	TAAAAAGTCCAGAAA[C/T]AGACTTACATACACA	9873
rs560915326	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72897985	ACTTTAGAAATCAGT[A/T]ACTCTCTTATGGAAA	9873
rs560928361	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72858125	CGAGGAAGGGAGAAT[C/G]CAGATAAAGAATCTG	9873
rs560940923	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72866362	GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC	9873
rs560995084	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73084445	GCCTAGGCTTGAGTG[C/T]GGCGGTGAGGTCCTA	9873
rs561037621	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:72957394	CTGCATAGTATTCCA[C/T]GGTGTATATGTGCCA	9873
rs561053497	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927334	TCATTATACATTTGT[C/T]TAAACTGAGAATGTA	9873
rs561053900	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73096189	AAAAAAATGCTGTCA[C/T]GAAAGAGATAATATG	9873
rs561054838	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72894380	TAGACCCCAGCTCTT[-/A]AAAAAAAATTAGCAC	9873
rs561056335	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075292	TATGACACAACAATT[A/C]CATTCCTTAGGTAAA	9873
rs561062913	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106475	GCTCTTAAATCAGTA[C/T]TCTGCTTGTTAAAGA	9873
rs561080298	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890788	GTTAAATGTTACAAC[C/G/T]TTAATTGACCGATTC	9873
rs561100237	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966265	CCCGGGTTCATGCAA[G/T]TCTCCTGTCTCAGCC	9873
rs561105350	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851492	ATTCCTGTAATCCCA[C/G]CACTTTGGGAGGCCG	9873
rs561108011	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72973096	AGTTATGGCCGGGCG[C/T]GGTGGCTCATGCCTA	9873
rs561120127	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982150	AAAGGGGATTTCAGG[C/T]AGTGAACAAAAAGGA	9873
rs561124983	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73075974	AAACACAAAAATTAG[C/T]CAGGCATGGTGGTGC	9873
rs561148169	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950383	GCTTGTGTTTTTGGT[A/G]ATATCTGAGAAACTG	9873
rs561156974	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837009	AATAACCCTTTGAGG[C/T]TGTGGAAAACCCAAA	9873
rs561164090	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898798	GCAGTGGTGTGATCA[C/T]GGCTCATTGCAACCT	9873
rs561171172	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72990291	TCAGCTGTGTTATTA[A/G]GCAACATTGCTTACA	9873
rs561179258	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844588	GGGGCTGGAAAGTCC[A/G]TGTGGCTTTGCTTCC	9873
rs561187303	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72998489	AGAGGTTGCTGTGAG[C/T]GAGATCATGCCACTG	9873
rs561188677	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72844017	TGTCTCTAAAAAAAC[A/G]AACAAAAAAAGAGAG	9873
rs561189731	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73000856	ACATGTTGAAATCAG[A/G]AAATCCTAGTAAAAT	9873
rs561201174	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73021234	ATCAAACATAGAATA[-/A]AAAAAAAAAAAAAAC	9873
rs561214313	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125827	AACAATTTCAATTGA[A/T]TCAATGTAACTAAGA	9873
rs561217899	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882923	CTATCTGATTTCAAG[A/T]CTTACAATGTCATTA	9873
rs561229973	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72959379	GGACTACAGGCGCCC[A/G]CCACCATGCCCGGCT	9873
rs561233301	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943205	CCCATGTTAGCCAGG[A/C]TGGTCTCGAACTCCT	9873
rs561245359	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72979907	GACAGTCATAATGAG[A/G]GTTGTTATCACCAAG	9873
rs561248575	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990874	AGAACAGAACTGAAC[A/G]AAATAGAGACACAAA	9873
rs561251597	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890132	GATCAGCATAAAACC[A/C]TTAAAGACCATAAGC	9873
rs561259922	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099384	ACCTGCTACAGAAAA[A/C]AGCTTGGCAGTTCCT	9873
rs561270621	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72936493	AAACTCAAGAATCTC[A/G]ACCAGGTGCCATGGC	9873
rs561282060	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72975261	CTTAGCTATTGTGAA[C/T]AGTGCTATAAGACAT	9873
rs561293871	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73114877	AGCTACAAGCTGTGC[A/G]CCCAAAACTGAGGGA	9873
rs561295928	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067168	CATAAAAAAGGATGA[C/G]TTCATGTCCTTTGCA	9873
rs561308972	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046653	AATATAGATAGACTT[C/T]GCTTACAAGGAAGCC	9873
rs561320817	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73092191	GGAGTACATTGGTGC[A/G]ATCATAGCTCACAGC	9873
rs561323609	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73060754	AAGCAAAGCTGTGGG[C/G]AAGATTGAAGTTAGA	9873
rs561323820	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869246	TTGTTTATATCCCTA[A/T]CAAAAAAAGGAAATC	9873
rs561344003	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876575	TAAACTTATTGAAAC[A/C]GGTTTATGGTCCAGT	9873
rs561355327	in-del	-/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72984818	CTAAAGACAACAGGC[-/T]GCCTAAGCAGGTAAG	9873
rs561364903	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982978	CCAGCCTGGTCAACA[C/T]AGCAAGACTCTTGTT	9873
rs561379194	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72970162	AGAAAACTCACTAAA[A/G]CCACAAATGGCTAAG	9873
rs561384579	in-del	-/CAAAGAC	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73084929	ATCACTGCACCAGTG[-/CAAAGAC]CAAAGACATAAGAGT	9873
rs561386570	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860939	GTTTAGCACTTAATG[C/T]CAATATTCAAAAAGA	9873
rs561398103	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73070107	TTATCAGTAACAAGA[A/C]TTTCATTGTCCCAAG	9873
rs561413558	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837874	AAAATAATGCCGGGG[C/T]GTCCCCAGTAGAGAA	9873
rs561416295	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029552	ATGGGAGCCAGGATG[A/G]GCAAATGGGACCCTA	9873
rs561429507	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877075	CTCCAGGCTGCCTCC[A/G]GTGCAGCCTCATCCT	9873
rs561440629	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73008600	GGATGAAAGCAGAAA[C/T]GGCCAGAGGTAAGTA	9873
rs561450860	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974477	ACTTTAGAGGACACA[C/T]TCAAACCATAACAAG	9873
rs561463756	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73079432	CTCGAACTCCTGATG[A/T]CGTGATCCGCCCGCT	9873
rs561481608	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141415	GCTAGAAACAAATCC[C/G]CCGCAAATTTGCAAA	9873
rs561482772	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73124915	AGAAAAAAGCTATTA[A/G]AGCAAGGGAAAGCAC	9873
rs561489019	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73077944	AGTCAGTATAGTAGA[C/T]TCCTTGAGTAAGAGT	9873
rs561491163	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73116161	TGAATCTTTACTGAG[A/G]TGATCTTATGGTTCT	9873
rs561526540	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080370	GACTTTAACTTTGAC[C/T]ACTCTGTAAAATGTA	9873
rs561527066	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73016236	TGAATCCAGGAGGCG[A/G]AGGCTGCAGTGAGCC	9873
rs561529845	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72868555	AATTAGCTAGGCATG[A/G]TATCATGGGCCTGTA	9873
rs561537565	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73110622	TTTCACAAAACCAAC[C/T]TTTCATTTTGTTGGT	9873
rs561541889	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140831	GCCCGCCAGGCCGGG[G/T]CCCCAGGGTTCGAAG	9873
rs561553137	in-del	-/A	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72919125	ATAATAATATAAAAT[-/A]AAAAAAATCTAAAAA	9873
rs561553907	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040277	GAGAAGCCCTCCTAC[C/T]AGAAGCTGTAATTGT	9873
rs561571912	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73067797	TTTCACATGAAATCA[C/T]TGAGAACAGTCTTAC	9873
rs561577707	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72860288	CCAACCTGACTTAAT[A/T]GACATTTATAGAACA	9873
rs561586379	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932527	ATGCAGTTTTTGGCT[C/T]CTCCAATACTCCTTT	9873
rs561591740	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970559	CTCACTTAAAAACTA[C/T]TGCTAGCACTCTCAT	9873
rs561593891	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962309	CGCTCTGACAGCTAA[C/T]GAAATCTGTACTTGG	9873
rs561622547	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73135593	CAAAGAGAAAAAAAT[A/G]TAATAATAAACTAAA	9873
rs561630032	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963143	TTTACGTGTGTTTTT[A/T]AAAAAATATTGTCTT	9873
rs561646856	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994413	TAGCAGCAGCAGCAG[C/T]AGTAGTAGTAGCAGT	9873
rs561674518	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72924472	TATTTTCAGTAGAGA[C/T]GGGGTTTCACCGTGT	9873
rs561675633	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72888746	CAACCTTAGCCTCCC[A/G]AATAGGTGGGAAGAT	9873
rs561684116	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111179	TGTTCTGTAACTACC[A/G]GGTCCATTCGGTCTA	9873
rs561685406	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039443	GACTCGCTTGAACCC[A/G]GGAGATGGAGGTAGC	9873
rs561686408	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121625	CTTAAGACAATAAAG[G/T]CTTAACAAAGAATCA	9873
rs561691917	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73101197	CATGACATTTATTCA[C/T]AAAAAGGCCACATAA	9873
rs561692717	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72871921	ATTTCCCTCCGAATT[C/T]TCTGCTTGGGGAGTT	9873
rs561703510	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878932	GCCAACATGGTGAAA[C/T]CCCGTCTCTACTAAA	9873
rs561716891	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73032476	AGTGATTCTCCCGAC[C/T]TGGCATCCCAAGGTG	9873
rs561720119	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72986240	TTAGAGACGGAGTCT[C/T]GCTCTGTTGCCCAGG	9873
rs561723274	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72928733	TTTTTTATTTTATTA[C/T]TATTATACTTTAAGT	9873
rs561724159	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895211	CTGGTGTGGACTGAG[C/T]CTTGGGACAATTCTG	9873
rs561730331	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73138432	AAATTATTACAACTA[C/T]TGACCACCCATACCC	9873
rs561732240	in-del	-/A	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73031473	AAGACCCTGTCTCCG[-/A]AAAAAAAAGAGAGAC	9873
rs561735930	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72863620	AAAGGATTTGTATTC[A/G]GAGTATAAACTCTTA	9873
rs561744824	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931825	CAAACATCTGTCAAA[C/T]AGAATTGCACAGACA	9873
rs561745461	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104302	GACAGAGTCTCACTC[C/T]GTTGCCCAGGCTGGA	9873
rs561751818	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73033138	CTAAAAATATAAAAA[A/G]TTAGCTGGGCATGGT	9873
rs561780008	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73061600	CAGCAGTCTGAGATC[A/G]ACCTGGGACGCTCGA	9873
rs561786714	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72924574	GACATGAGCCACCAC[A/G]CCCCACCCAGCTATT	9873
rs561800757	snp	A/C/G	4.98694e-05	0.00499326	intron-variant	FCHSD2	GRCh38.p7	11:72849917	AGAAACCATTGGCTA[A/C/G]TTTCCTTACTTCAAG	9873
rs561802600	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995173	TTCATTCCTTTTTAT[C/T]GCCGAATAGTATTTT	9873
rs561810419	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122498	TTGATCTGCTCTTCA[A/G]AACACAGGAATGGCT	9873
rs561812960	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025952	ACTAAAAAACACAGA[C/T]ATGCTCCATGTTTTG	9873
rs561816780	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130178	CGCGCCTGGCCCATA[A/G]TCTCTTATATTTATA	9873
rs561837221	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73041035	GACCTCCAGTTCCAT[A/C]CATGTTGCTATAAAT	9873
rs561860830	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72888407	GGGAAGGAAAGGACA[C/G]GAAAGCTCAAATGTA	9873
rs561866636	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73010937	TGATGGGATAATCTT[C/T]TGGGTCTTGAGCAGT	9873
rs561870324	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033676	CTATGGAATTCTATA[C/T]AAATTTATATAATTT	9873
rs561873753	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73026887	ACCATGTAAGACATG[C/G]CTTGCTTTCCCTTTG	9873
rs561877607	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137930	ACCTTTATCCAGAAG[G/T]CCACAGAGGAGTGAT	9873
rs561880510	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72979232	TGGTAAGGATGTGGA[A/G]AAAACAGAACTCTCA	9873
rs561881772	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129884	AATCTTTTTTTTTTT[C/T]TTTTTTTTGAGACAG	9873
rs561897864	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73072909	TAAAAATAGCAAAAA[A/G]TTTTAGGTGCAACAG	9873
rs561901278	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73071103	TAAAAGATGGTCTAC[C/G]AATTATTTTACAAGA	9873
rs561901396	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925261	ACCATAATCAGGATC[A/C]TTTCTGATTATAGAT	9873
rs561909510	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72954951	GATAGGAAAAAACTG[A/C]AGTGCTTTTTCTACC	9873
rs561927506	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72904118	TTAATCCAGGCCGAT[A/G]ATGGGGTGAGATGAG	9873
rs561930730	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909788	GGGAACTGAGGAGCA[C/T]CTCTGCCCGGCCGCC	9873
rs561932617	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72916594	TATTGGGATTACAAG[C/T]GTGAGCCACTGTGCC	9873
rs561936599	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144010	GCCCTGACAGCTGCG[C/G]GGTGGCAGCTAGAGC	9873
rs561939918	snp	C/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:72988385	TCTTTTCCTACTTAT[C/T]CTTAAAAAAAGGTCT	9873
rs561944189	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73137325	AAGAACACACTAACT[C/G]CTTTAAAAAAAACCT	9873
rs561951069	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947637	TCCCATCCTCCAGCA[C/T]ATTCTGTTGGAACAG	9873
rs561964692	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72872549	AAACAATATAATACA[C/T]GGTCTTTTATGACTA	9873
rs561977608	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989211	ATCCAGGGGAAAAGT[C/G]AGTACGTTCAGTGTC	9873
rs561981817	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881259	ACATAATGGCCAACA[A/G]GTATATGAAAAAATA	9873
rs562009294	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72956205	CCATGGACATAATGA[A/T]ATAAATAAATAAACA	9873
rs562067844	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73097166	CACCACCAGGCCTGG[C/G]TGATTTTTGTATTTT	9873
rs562070132	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881948	AGATTGAGACCATCC[A/T]GACTAACACGGTGAA	9873
rs562091358	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73136565	TAATAATAATAAAAA[A/G]AATTATCTACTACTA	9873
rs562102142	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041887	AGTAGTTTTATAGTT[C/T]TGGGTCCTAGGTTTA	9873
rs562104398	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73122413	CCAGGAAAGCAGGTA[C/T]ACAGGCATCCCCTCA	9873
rs562105186	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011659	GCCATCACACAATCT[C/T]CTGGCAGCTCCCTAT	9873
rs562116565	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73109066	TGGATTTGCTTTTGG[A/G]TTCTCTATTCTGTTC	9873
rs562132699	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73089431	CAATTCTATTCCTAG[C/G]TGTATATCCATGAAA	9873
rs562137374	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73006446	ATTGATTCCTCATTT[A/G]TCTATCATATCTGCT	9873
rs562154037	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73106766	TGCTTAAAGTATTCA[C/G]TACAGTAACATGCTG	9873
rs562166562	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121360	ATTATTCCCACTCTA[C/T]ACAGATGAAGGACAC	9873
rs562167760	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73003261	TCAACTGGCAAATGG[A/C]GAAATAACAAAAATA	9873
rs562184062	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72905175	TTTAATTTCTTCTGA[C/T]GGTAATTATTGTCGG	9873
rs562197387	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941452	TTGGATGTCAGTTTG[C/T]TTAGTATAAAATATA	9873
rs562197947	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72926837	GTTGATAGTTTTGAA[A/T]TTAGATGTAGAAGCA	9873
rs562198853	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853004	GAAGGCAGAAGGTGG[A/G]AGGAGGGAGAGGATT	9873
rs562198855	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998686	TAAGAAGCTAATAGT[A/G]GAGGAAAAAATTGAT	9873
rs562199319	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73007399	GCTGAGGCAGAAGGA[C/T]TGCTTGAGGCCAGGA	9873
rs562208746	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73095340	TAAGTGACAATATCA[C/T]ATTCCACAGCTTATA	9873
rs562221153	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72896981	ACAGGTGCCCGCCAC[C/T]ACGCCCGGCTAATTT	9873
rs562229425	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841979	CTGACTTCCCCAGGT[A/T]TTGTGCATGTTAGGC	9873
rs562237297	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72865376	TATTATTAGATCTTC[A/C]ACAAAATGTAATCTC	9873
rs562241608	in-del	-/TCTGTTCAGACCA			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143511	CATGAACCTTCCTGC[-/TCTGTTCAGACCA]TCTACGGGGGAGTTT	9873
rs562242563	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72886109	GGTGTTAGAAAACCA[C/T]TAGTTTAGTTTAAAC	9873
rs562255277	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72891005	TCACTGCAGCCTCAA[C/T]CTCCGGGCTCAAGTG	9873
rs562257730	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73007275	TTTATGAATATCATA[C/T]AAGATATCTAGGAAA	9873
rs562259109	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73032447	CCAAGGTTGGTCTCA[A/C]ACTCCTGGCCTTAAG	9873
rs562259604	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72999244	TGCTTAGATGTAACA[C/T]AGATCATCAGCAATA	9873
rs562269939	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72873898	ATCAAAAACTGCCAA[C/T]TACCTTCTAACTAGA	9873
rs562271861	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72889327	TTCAACATATGTCTC[C/T]TCCCCTGCCCATAAT	9873
rs562286444	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72917384	GCACCTTTGTTGCAA[A/G]TCAATTGACCATAGA	9873
rs562294337	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112893	CTCGTCTTGAACTCC[A/T]GACCTCAAATAATCC	9873
rs562309312	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72962763	CAGGTTAAAATAAAA[A/T]AAAAAATCACACCAA	9873
rs562332145	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73120369	AAGTCTATTAAGTAT[A/T]AATTGGCCAACAATG	9873
rs562346779	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73107258	CAGGGTTTCACCATG[C/T]TGGCCAGGATAGTCG	9873
rs562354880	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959293	GGAGTGCAGTGGCCC[A/G]ATCTCGGCTCACTGC	9873
rs562356630	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72997787	CTTCCTGCAATCTCT[A/G]CCTCCTGTGCTCAAG	9873
rs562360473	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73090454	ATGGTCTCGATCTGC[C/T]GACCTCGTGATCCGC	9873
rs562377488	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73120900	GCACTGGATGTTATG[A/G]GAACACACAGGCAGA	9873
rs562389466	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971531	ACATGAACAGGACTG[A/G]ACACACTACTGCTGG	9873
rs562393211	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035206	TATGTATGTATGTAC[A/G]TACTAAGACAAGGTC	9873
rs562397118	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73128937	AGTGTAGTGGTGTGA[C/T]CTCAGCTCACTGCAA	9873
rs562414145	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72908136	GAACATGTGAAATTT[A/G]TCTTTCTGTGCCTAG	9873
rs562438789	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951784	TTGATTTGAGGTTTA[C/T]CCTTTCACAATCTCT	9873
rs562442277	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73021466	GCAAGAACAGAAAAC[G/T]AAATAATATATGTTC	9873
rs562455093	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900625	CCAGGCTTCAAAGAA[G/T]TCAAATCACAGGAGA	9873
rs562461078	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72845543	CAATGTAAGCAGACA[C/T]TAGCTTGATCATCCC	9873
rs562466244	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885457	AACTAACAAACACAG[C/T]CTAGTTTGGCATACT	9873
rs562492150	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129078	AGATTTCACCATGTT[A/T]GCCAGGATGGTCTCG	9873
rs562502229	in-del	-/AAGG	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72883058	GTAATGGGAAAAGCA[-/AAGG]TACTCTTTAAAATAT	9873
rs562509853	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72998086	TACACAGAGAAAAAA[C/G]GGTGGAAAACAAAAT	9873
rs562511782	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73037373	TAGTGACATATCCAT[C/T]ATTACAGTATCATAG	9873
rs562513301	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951145	ACTCCAAACCATTGC[A/G]TTAGAAATAATTAAC	9873
rs562519702	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898564	GAGTATATAGTTCTC[C/T]ATTTACCATCATATA	9873
rs562532450	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101167	CTGAGGTTTAGTTCC[C/G]ACCTGAAGGAGAAAC	9873
rs562557852	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844793	AACAAAAATAAGGCA[A/G]AAAAGGGGTCATTTT	9873
rs562558807	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052627	AAACAAATTCTTAGT[G/T]TTTCTGCAAGATAAA	9873
rs562569534	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838109	TGGCTACTAGTTCAG[C/G]CCCTCCATATTAGCT	9873
rs562577359	in-del	-/GTT			intron-variant	FCHSD2	GRCh38.p7	11:73041595	TTATGGAGTTTTTTT[-/GTT]TGTTTGTTTGCTACT	9873
rs562578024	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900160	CCTCTTATACATGTA[C/T]ATACATAACTTTCAT	9873
rs562588493	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129763	CATGGGAAAACTGTC[C/T]TCCAGGAAACTGGTC	9873
rs562601174	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914617	TCTTCAACAAACCTG[A/T]CAAAAAGCAATGGGG	9873
rs562604126	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944519	CTCTCTCACCACTCC[C/T]ATTCAACATAGTGTT	9873
rs562608719	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025008	AGAAGTTGGCAAGGT[C/T]GTGGAGAAAAAGAAC	9873
rs562627602	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038543	GAAATCTTGTCCTTT[C/G]TAGCAACATGAATGT	9873
rs562629065	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73100138	CATGTGCTGCCCCCA[A/C]CACTCTTCTCACTCC	9873
rs562631823	in-del	-/AT	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73077170	TCGTTCTACTTTCAC[-/AT]ATGTTTGAAAACTTT	9873
rs562642395	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73011994	AACATTTTAAATATA[C/T]AAACCCTTTGATCCA	9873
rs562651284	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137198	TCAATATTGTCTTTG[A/G]AAAAAAAAAGCAAAT	9873
rs562661192	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093163	TACTGTCACACATCA[C/T]TGCAGAAGAAGTGAA	9873
rs562662362	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72984707	GAAAAACTCACTCAC[A/C]TCTGGCCCAGAATAT	9873
rs562670921	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930645	AATTATTTGGGAGCC[C/T]GAGGCATAAGAATTG	9873
rs562680219	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72855689	TTACCCATCATAGCT[A/G]AAAGGCATTTATTAA	9873
rs562691192	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72924324	GCTCTATTGCCCAGG[C/T]TGGAGTGCAGTGGCA	9873
rs562726992	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037858	GTGGACAACTTTAGG[A/C]AAAGAAGAAGGCAGT	9873
rs562728689	snp	A/C	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72937979	TCTGAATGGTAAGGG[A/C]AACAACAGAATAATG	9873
rs562757336	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930031	AGAATGAGGCATTTA[C/T]CTTAATTGGGTCACC	9873
rs562759773	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72922804	ATTCACCCAATATAA[A/G]TCACCATTTTAATAA	9873
rs562772118	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73069466	ATACATATATACACA[C/T]ATCTCTAAAAAGAAC	9873
rs562793401	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73041839	TTTTTGCCTAGGCCA[A/G]TGTCCTGGAGTATTT	9873
rs562819792	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73137939	CAGAAGGCCACAGAG[A/G]AGTGATCTATAATAA	9873
rs562837216	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72945951	ACACTGTTGGTGGGA[A/C]TGTAAACTAGTTCAA	9873
rs562842709	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73070031	TGAATTTCCAGGTGG[C/T]GAAAGTAAAAAGGGA	9873
rs562856542	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841666	ACTGCTCTGTACTCA[C/T]GCCTTTTCTCTAAAG	9873
rs562871397	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017014	TTGAGACAAGGCCTC[A/G]TTCCAATGCCCAGGC	9873
rs562873366	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72895176	TGCCTGGCCTCTCAG[C/G]AGAGCACACTGGAGA	9873
rs562875002	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946415	GTGGGGGAGGGGGGA[A/G]GGATAGCATTTGGAG	9873
rs562876635	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73077152	AAAGTTTGTTACGCT[A/C]ATTCGTTCTACTTTC	9873
rs562904275	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113662	TCGTCATAGTCTGGG[A/C]TTGTTTGTACCCGTC	9873
rs562908353	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73078008	CTGGGATGCTGTTAA[C/T]GTGTTTCTTTACCTG	9873
rs562936980	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862028	ATCATCAATGCAATT[A/G]CACCATATTAGCAGA	9873
rs562937285	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72973999	AGGAGCAATTAATTG[C/T]GAAATAATCAAATAT	9873
rs562940411	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73068736	ACACTTTGGGAGGCC[A/G]AGGCAAGAGGACTGC	9873
rs562948220	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953381	TTCTGCTTTCTGAAA[C/T]ATCTACATTTGGAAA	9873
rs562957319	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969018	TGATATACACACATA[A/T]ATACATATGCTACTA	9873
rs562965943	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72926604	GAACACTCCAAGGGA[C/T]GATATGCCTACAGAG	9873
rs562967617	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112809	ATACACTATCATGCC[C/T]GGCTAACATTTATTT	9873
rs562987496	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72960147	CTGGTGAGGCTTCTG[A/G]AAGCTTACAGTCATA	9873
rs562995711	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847432	CGTGCTGGGCATTGT[C/T]CTAGGGGCTGAAGAC	9873
rs563026577	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126895	ATAAAAAAATTTGCC[A/G]AGCATCGTGTTGCAC	9873
rs563031596	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119710	CCTTGGCCTCCCAAA[G/T]TGCTGGGATTACAGG	9873
rs563050440	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72894575	TATGAAGTATATTAA[C/T]ATATGGTTAATTATT	9873
rs563052633	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839688	GGGAGAAGGAACATG[C/T]CTGGAAGGGAACATA	9873
rs563068159	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952627	ACCATGCCTGGCCTA[C/T]AGTTAATTTTGGTAA	9873
rs563074975	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109531	TTCACTGTTGGCATA[C/T]AGAAATCTTACTGAT	9873
rs563078798	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72952275	CTAGTATTTTTAGAG[A/C]AAAAACAATTCCATA	9873
rs563082282	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72901663	TTAAAAATGGTAATT[C/T]TTGTGTTATGTGTAT	9873
rs563086769	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134598	GAGGTCTCTAGACCA[C/T]CAGGTGTCTGCAAAG	9873
rs563089138	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72918054	ATTATATGCATTTAT[C/T]TATATCTTTTATTTC	9873
rs563098953	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119289	GCCTGCACAACAGAG[C/T]GAGACTCTGCCTCAA	9873
rs563114888	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081603	ACTATCTGAGCTCAC[A/T]GCAATCTCCGGCTCC	9873
rs563132107	snp	A/T	0.000399281	0.0141238	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73000997	AACAATACCCTTTTT[A/T]GTTGCTGTTCTTTTA	9873
rs563136950	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72966926	GAAAGTGGCCGGGCG[C/T]GGTGGCTCACGCCTG	9873
rs563140222	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73110201	AGGGTACTGCTGGCC[C/T]CACAGAATGAGTTTA	9873
rs563142324	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010368	CTTCTTTAATATCAA[A/C]ATTTTGAATTCTTTT	9873
rs563159377	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102303	ATATAGATAGACTCT[A/G]GGGAAATTTTTGGCA	9873
rs563168518	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058083	ACAGGGTTTCACCGT[C/G]TTAGCCAGGATGGTC	9873
rs563176081	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73072365	GAGTACTAACATTTA[A/G]TTATAGCCACCATTT	9873
rs563183798	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135389	TCCACCTGACTAAAA[C/T]TCAATAATTTTTCCA	9873
rs563193470	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72993936	TAAATAAATATCGGA[A/T]AGAAAAGCCAGGCTT	9873
rs563193561	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73001978	TATTTATAAACACAA[C/T]CGATAATTTATAACA	9873
rs563205721	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019878	GCCTAATTAATTTGC[C/T]AAGGAAAATAAACCT	9873
rs563241373	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73058779	TACCATGTTGGCCAG[G/T]CTGGTCTTGAACTTC	9873
rs563246812	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72989761	ACACTGCCTCAGGAC[C/T]TTTCTGAGTATCCAA	9873
rs563249980	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73070313	CACTCTGTTTTACTG[A/G]TAACATTCCAGCACT	9873
rs563284749	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910793	CTGCCACATCCCCCT[C/G]TCCGAGAAACACCCA	9873
rs563309694	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72942327	GAAGCAGATGCCAGC[A/G]GCATGCTCCCTGTAC	9873
rs563310095	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955855	GAGACCAAACATGTA[C/T]TTCAAATTATAATAT	9873
rs563320275	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905312	ATATAGTAGGTATTT[A/G]TATTTATGGGGTACA	9873
rs563320999	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971416	TTGTGATTATGCTAC[A/G]TTAAATGGCAAAAGG	9873
rs563321299	in-del	-/CGCTCCCGGTCGGCCGCCTGCGCCGC	0.0244538	0.107838	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142235	CAGCCGCGTTGTCCG[-/CGCTCCCGGTCGGCCGCCTGCGCCGC]CGCTCCCGGCGGACG	9873
rs563330558	in-del	-/TGATGCTAGAACAAT	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73022964	GTCTCAATCAACAAG[-/TGATGCTAGAACAAT]TGAATGACCATAAAC	9873
rs563336705	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72852375	CCCATTACTGGACAC[A/G]TACCCAAAGGTACAT	9873
rs563348156	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943107	AGTGATTCTCCTTCC[C/T]TGGCCTCCTGAGTAG	9873
rs563352250	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138730	TCTCTGCCTCAGCCT[C/T]CTGAGTAGCTAGGAC	9873
rs563361656	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73027644	AAAAAGAAGCCAAAT[A/G]TTAATAGCCAAAACA	9873
rs563397957	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091558	CATCTCAAAAAAAAG[A/G]AAAAAGAAAAGAAAG	9873
rs563423343	snp	A/G	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73049698	ATAAAAAAAAAAAAA[A/G]AAAGAAAAAGGGGGA	9873
rs563428955	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73020508	ACAATGAACAAGTTC[A/G]CTGCATAAGCTGGAT	9873
rs563434210	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116979	TATTGTTATATCTCT[A/G]TTTCATTTTTAGCAT	9873
rs563452718	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72857365	GTCACTTGACAGAAC[C/T]TCAATCAAAACTATT	9873
rs563454394	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72866229	ATAGTAGGAGATATT[C/T]CATGAGATGGAGCAA	9873
rs563461015	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092086	TCTGAGAAGCCTTCC[C/T]GAATTCCTCTTGTGA	9873
rs563464328	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098240	ACAGCGTAAGTTTTG[A/G]TATTGTATATTTTTG	9873
rs563470065	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72964883	CAAGTTCTGCCTCCC[A/G]GGTTCACGCCATTCT	9873
rs563490563	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73013017	CTTCCTCACACCCCT[A/C]GAATCCACCTTTACA	9873
rs563498037	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116427	TGGGTGTTTTTCTCA[C/T]TCTGTGAAACATTCC	9873
rs563502477	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72973547	TATCACAGGGCATGA[C/T]ACTATCTAAGACAAC	9873
rs563506449	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956527	ACTTATAATCAACAG[A/C]ATTAATTTCTCTTAC	9873
rs563509998	snp	A/C			intron-variant, upstream-variant-2KB, utr-variant-5-prime	FCHSD2	GRCh38.p7	11:73141051	TCATCCACCCAGTGC[A/C]CAGAGTAGACATTCA	9873
rs563526271	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004474	CTAACAGTTACTCAG[G/T]CCTATAAGAACCCAC	9873
rs563527274	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72898755	TTTTTTTAAAGACAG[C/G]GTCTTGCTCTGTCAC	9873
rs563529432	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72989499	TATGTTTGGGTAACC[A/G]ACAGTGCAAAGGGTA	9873
rs563544130	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72867624	TTGGTAGATAGGCAT[C/T]GATAACCCAAATAGT	9873
rs563553208	in-del	-/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72986635	TATTCCCAGTTCTCC[-/T]TTTTTTTACAGTCAT	9873
rs563566111	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72843858	AAATAAATAAATAAA[A/G]TTAGTCAGGCATGGT	9873
rs563570925	in-del	-/A	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73131528	GTGAGACTTCGTCTC[-/A]AAAAAAAATAAAAAT	9873
rs563585834	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123596	TATGTTTAATTCTGG[A/G]AATTCAAAATATTTC	9873
rs563589682	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997383	TAGCATTCTATCCAC[C/T]TGCCAGAAGAAAGCT	9873
rs563591349	in-del	-/AATA	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73055671	TCACTTAAATTTTTT[-/AATA]GATAAAACATACCAT	9873
rs563605341	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72859011	TTTTAGGTTATGACA[C/T]AGGGAGAAGAAACCC	9873
rs563621415	snp	A/C/G	0.000462897	0.0152069	missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843170	GGCATCTCCGTTGAG[A/C/G]CTGCCTGAAACGAGT	9873
rs563624490	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966252	GCAACCTCTGCCTCC[C/T]GGGTTCATGCAATTC	9873
rs563638326	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115512	TCCAACTCTATACTT[A/T]CGTGTCGTTTTCATG	9873
rs563661765	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051082	ACATTTTGGGAGGCC[A/G]AGGTGGGAGGATCGC	9873
rs563670251	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72880123	AACAAAAAACCCCAA[C/T]CCCAGGAATAAATTT	9873
rs563705177	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890027	GATGGATCAGAAGGC[C/G]TTCACTTAATCAGCA	9873
rs563732024	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102223	AGAAAATTAACAATT[C/G]CAAGTGCTGATAAGG	9873
rs563733061	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021771	AGATGCAGAAGAATA[A/C]GTCCTTAACCTAATA	9873
rs563733835	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72911246	TTATTGAAGAGATTG[C/T]CCTTTCTCCAATGTA	9873
rs563744279	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72945802	ATGAAAAAATGCTCA[C/T]CATCAATGGACATCA	9873
rs563748006	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73035985	CAGCCTCCCAAAGTG[C/T]TGGGATTACAAGCGT	9873
rs563775873	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72876238	GGGAGGCTGAGGTGG[C/G]AGGATTGCTTGAGGC	9873
rs563793101	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73083650	CTGTCCTTAAGCCAC[A/G]GAAAAGAAGTATACC	9873
rs563796409	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72868116	ATGCCCATCAATGAT[C/T]GACTGGATAAAGAAA	9873
rs563813641	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028937	AAGCCACGTGAAACT[A/G]TGAGTCCATGAAACC	9873
rs563819935	snp	A/G	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73093762	ATGCACCACCATGCC[A/G]AGCTAATTTTTTTTG	9873
rs563837415	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928085	GTCTTTCTTGCCTTG[A/C]TTTAAAATCATCAAT	9873
rs563837940	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839485	AATCCTCTGAATGAG[A/C]GTTGACAATAGCCCA	9873
rs563862635	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986159	AAAAATTGGGTTTAA[A/G]AGATTCCTGTTATTT	9873
rs563862794	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72846169	GATGAGTAAGCTGCT[C/G]CTCCTTTTGCTCTTT	9873
rs563863558	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875482	GGGACCAGAAGCATA[C/T]GCCACCACATCTAAT	9873
rs563874327	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029461	GCTCTTAGCTCAGCT[A/G]TGGCTACCCATCTTT	9873
rs563899349	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72977667	AATCACTAAAAAGTC[A/G]GGAAACAACAGGTGC	9873
rs563900933	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73024518	AAAAGCTCAGTGTTG[C/G]AGTGGGACTTAGAAA	9873
rs563901925	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000894	AGAAACATATGGGAC[C/T]ATATAGTTTTAAATA	9873
rs563924067	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73087648	AGGCAGAGGTTGCAG[C/T]GGGCCGAGATCACAC	9873
rs563926430	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986505	TGAGCCACCGTGCCC[A/G]GCCCCAATTATTTTA	9873
rs563929243	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920527	GGTGGACCACTTGAG[A/G]CCAGGACTTCAAGAC	9873
rs563937033	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73057822	GTTCCCCTCAGTTCT[C/T]GAGGGATCTAAGAGG	9873
rs563941863	snp	C/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:73045774	GGACTGTTGTGGGGT[C/G]GGGGGAGCGGGGAGG	9873
rs563945308	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73075227	AAATTGCAATAATCA[C/T]CTGAGAAAACCATTT	9873
rs563965617	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978621	ACTGGATTATAGGAG[C/T]GATTTCCCTGATGCT	9873
rs563968857	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72919561	CATATAAAATGAACA[C/T]GGTAATGGCGACCTC	9873
rs563983811	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72870769	GCTGGGCGTGGTGGC[A/G]GGTGCCTGTAGTCCC	9873
rs564008667	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862937	ATATATGATTAATTT[G/T]TTTTTTAAAGAGACT	9873
rs564012068	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73067017	ATAAATCATTCTACT[A/G]TAAAGACACATGCAC	9873
rs564020678	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72871738	CACTCCAGTGACAAA[C/T]ACCTTTGGTACATAA	9873
rs564054547	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72931689	AGAATTGCTTGGACC[C/T]GGGAGGTGGAGGTTG	9873
rs564061360	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73045159	GCAGCCAAAAAACAC[A/G]TGAAAAAATGCTCAT	9873
rs564068271	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893357	TTCTCACTCTATTGC[C/T]CAGGCTGGAGTGCGG	9873
rs564068384	snp	A/C	0.000155328	0.00881134	intron-variant	FCHSD2	GRCh38.p7	11:72902511	AAACACAACTGAACA[A/C]CACATGAAATGAAAA	9873
rs564102953	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116923	AGAGTAATTATATTT[C/T]TTCATGTAAAACCTT	9873
rs564113323	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72963921	ACAACTCTGTGTCAT[A/G]AATAGATTTCACAGT	9873
rs564171013	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72997400	GCCAGAAGAAAGCTT[A/C]ACCCTCTTTGGAAAT	9873
rs564177692	snp	A/C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72893465	AGACCACAGCATATG[A/C/T]CATCACACGCAGATA	9873
rs564193619	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025856	ACCAACTCAGTAACA[C/T]CCTTCTGGTCTCCCG	9873
rs564203322	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73116362	TTTGATTGCTTGTAC[A/T]GTCCTGTTAGATTGT	9873
rs564207897	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138660	GTTGCCCAGGCTGGA[A/G]AGCAGTGGTGCCATC	9873
rs564208734	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73032496	ATCCCAAGGTGCTAG[C/G]ATTACAGGTGTGAGC	9873
rs564211100	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040173	GGTGGCCAGTCTGCA[C/G]CTCTGTGTCAGCAGC	9873
rs564224963	snp	A/C/T			intron-variant	FCHSD2	GRCh38.p7	11:73069843	AATAAAACATCTAGA[A/C/T]TCATAAATGATACAT	9873
rs564236016	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73003733	CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA	9873
rs564237149	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72969599	GAATACAAGAAGCAT[C/T]GAAGATATAAAAAAC	9873
rs564239887	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73127967	CCAGGCGTTGTGAGA[G/T]CACACCACTGTACTC	9873
rs564249103	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017785	GCTAAATTCTCACCC[C/G]TCCCTTTTAATCTGA	9873
rs564274824	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73025506	GGGTGGAGGGTGGGA[A/G]GAGGGAGATAATGAG	9873
rs564277024	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73124027	AATGTCCATCAATGA[C/T]AGACTGGATTAAGAA	9873
rs564278477	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73033017	AGATTGGCCGGGTGC[A/G]GTGGCTCACACCTGT	9873
rs564294699	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923917	GAAATACAGCTCTGC[A/G]TGACAGAGCAAGACT	9873
rs564294829	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131244	AAAATTAGGCCGGGC[A/G]CAGTGGTTCACGCCT	9873
rs564308740	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909723	GCGCCTCTGCCTGGC[C/T]GCCACCCCGTCTGGT	9873
rs564311992	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025199	CACACATATGTTCAC[G/T]GCAACACTATTCACA	9873
rs564333289	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72924393	TGCCATTCTCCTGCC[A/G]CAGCCTCCCGAGTAG	9873
rs564334274	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72896310	GGGAAACCTGAGGAA[A/G]TTTCCGTGTTTTTCC	9873
rs564348751	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879475	ATGACAGAGATGATG[C/G]AATGAGTAGACAAGA	9873
rs564354199	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130420	CTATTCTTAACCCTA[A/G]AGATAAGTAACTTTC	9873
rs564354708	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73041065	TGACAGAATTTCATT[C/G]TTTTTTATGGCTAAA	9873
rs564368847	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855682	AGGTATATTACCCAT[C/G]ATAGCTAAAAGGCAT	9873
rs564369591	snp	A/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72898600	CTCAAAAATAACACC[A/T]GGTTGCATCCCACTT	9873
rs564370520	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72888203	GAAAAAATCTAGGTA[C/T]GGCCAGAAAGGCAGA	9873
rs564388282	in-del	-/TCAAGA	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73032781	GGGAACATAGCCCCT[-/TCAAGA]AACTTCATACAAGCT	9873
rs564391399	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111011	ATTGATTTCTAGTTT[C/T]ATTCCATTGTGATCA	9873
rs564393493	snp	C/T			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144431	GAGGCAGGAGAATAG[C/T]GTGAACCCGGGAGGT	9873
rs564398752	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903470	GTGATCCACCGGCCT[C/T]GGCCTCCTAAAGTGC	9873
rs564405351	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72922855	TGGCTTTTAGTACAC[C/T]GACAAAGTTGTTTAA	9873
rs564420075	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72916025	AAATTATGAGAACAC[A/G]TGGGAACAACGCACA	9873
rs564422477	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72890050	AATCAGCACTCAAAA[C/G]ATGAGGCACGCTCCA	9873
rs564431834	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73121176	ATACACATACACATA[C/T]ACACACACACACACA	9873
rs564463191	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72848981	GAAGTATTATGAATT[C/T]AAATATAAAATGAAA	9873
rs564473242	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925537	TCTTTAAAACAAACA[A/G]ACAAACAAATAAATT	9873
rs564479053	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73034712	AACTTCAATAAACTT[A/G]TTTGCACAAAATGAC	9873
rs564494233	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018827	AAATTTGACCATCTT[A/C]ACTATTTTAAGAGAA	9873
rs564498808	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995092	ATATGTGGCCTTATG[A/T]TTCTCACTTCTTTCA	9873
rs564503709	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72982280	ACTTTCAAGGAAAGA[A/C]CTTGCAGTTTCTGGC	9873
rs564510184	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110354	GATATTTTATTACGG[C/T]TTCAATCCTGTTATT	9873
rs564513640	snp	A/G	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:72861919	CTGGGCAACAAAAGC[A/G]AAACGCCGTCTCAAA	9873
rs564528720	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014061	AGAATTTCATCTCTC[C/T]TCTCTTCCTCCTTAG	9873
rs564540235	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055378	ATAAAGAAACACTGA[A/C]GTAAATACTAATAAT	9873
rs564546925	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142059	GACCCCAGCCAGAGA[A/G]CGAGTGTGAGGAGAC	9873
rs564551523	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946797	CATTTTCATTTTACA[A/G]AGCAGGAAACTGAGT	9873
rs564551627	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954909	ATATATACAGAAACA[C/G]ATCTGGCTGTATGTA	9873
rs564560959	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987730	CCTGTGGGCTGTGGC[C/T]AAATTATTTGTTTAT	9873
rs564565518	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73020699	TATTATTTTAAATTA[C/T]ATAATAAATTGTCTT	9873
rs564578813	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910017	TCTAGGAAGTGAGGA[A/G]CGCCTCTGCCCGGCC	9873
rs564586411	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72880426	ACCAATGGAACAGAA[C/G]AGACATCCCAGAAAT	9873
rs564615732	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72904030	ATCTGGGAACTGGGC[G/T]AACCAAACAGACTAC	9873
rs564617030	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72933302	AAGTTATTCTTCCTA[C/T]CAAGCAGATAGTGCC	9873
rs564619126	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73113836	GCTATGTTTCTTGAA[A/C]ACTTGTAGTGGTACT	9873
rs564633049	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73131850	CTTATTAAAAGAGTT[A/C]TTTTAAACTTATTTA	9873
rs564634419	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72994155	GACCGAGACATACAA[C/T]AGTGGGAGAATTATT	9873
rs564644417	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880440	ACAGACATCCCAGAA[A/G]TAATGTACTTATAGC	9873
rs564670288	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840293	ATGAAGCCAAAAGAA[A/G]CCAGTGGTAAAGGAA	9873
rs564694943	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73099270	AGGATGGCTGTAAAA[C/T]AACACAAAACAAAAC	9873
rs564696286	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73104809	CTGACCTCAGTGATC[C/T]GGCCTCCCAAAGTGC	9873
rs564713464	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72954323	ATGCAATTCTCTCAA[C/T]TCAGCCTCCTGAGTA	9873
rs564723888	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73097079	ACAATCTCAGCTCAC[G/T]GCAGCCTCGACCTCC	9873
rs564723974	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088587	GTTTTAGTAAACATA[C/T]AATGTTTGAAAAAAA	9873
rs564727193	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73031891	CACTGTATTAGATGC[C/T]GGGGGAATAGCAATA	9873
rs564737496	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022450	ATATTCCAAAGTTAA[C/T]TGCTCTCCTACATAC	9873
rs564753573	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044133	ACTGATACATCCAAG[A/G]CCTGCTACTATATGT	9873
rs564760860	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72941286	TAAATATTTGTTAAA[A/T]TATGAATTAATGAAT	9873
rs564764106	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059030	CCATTTTAGTTTTTA[A/T]GCTAAGCTAAGAAAT	9873
rs564772243	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966183	TTTTTTTTTTTTCAG[C/T]TGGTCTCACTCTGTC	9873
rs564787214	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73089322	GAAATCAGAACTCTC[A/G]TAGCGTTAGTGGAAA	9873
rs564791775	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73061087	GCAGAAGGCAGATGA[C/T]TTCTGCATGTCCAAC	9873
rs564795664	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72851599	AAACAAAAAATTAGC[C/T]GGGCATGGTGGCATG	9873
rs564816913	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037010	TAGGGACTGCCAAAT[A/G]CTGATATCAATTCAA	9873
rs564824825	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988301	TTATCTTTCCTCAAA[C/T]TGTCACTGCAAAAAT	9873
rs564832304	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907274	TACAATCATGTCATC[G/T]GCAAAAAGACACAAT	9873
rs564848859	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965533	GTACATACTGCCATT[A/G]TAGTATTTTTTTAAA	9873
rs564851276	in-del	-/TTTTT	0.00875682	0.0655876	intron-variant	FCHSD2	GRCh38.p7	11:73110151	TCTGTAGTTTTCTTC[-/TTTTT]TTTTTTGATGTGTCT	9873
rs564866255	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73023314	AAAGGAAGTCCAAAT[A/C]TATAAAGAATTCCTA	9873
rs564879535	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72879134	ACAAAACAAAAAAAC[-/A]AAAAAAAAAGATATT	9873
rs564883005	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72912770	GGCTTTTCCTTGCTG[A/G]GAGACTTTCTATTAC	9873
rs564894734	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125621	GAGGCAAGAGGACTG[A/T]TTGAGCTCAAGGGGT	9873
rs564905930	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73066925	TGGAAGACAGTGTAG[C/T]GATTCCTCAAGGATC	9873
rs564923052	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73054066	ATTCTAGCCTGCTGT[C/G]TGTTTCACTAAATAA	9873
rs564926936	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73108026	GTACTAATTTACATT[C/T]CCACCAACACTGTCT	9873
rs564930348	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72933973	AATTAGCCAGGTGTG[A/G]TGGTATGTGGCTGTA	9873
rs564930448	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73000129	ATCATCTTTGGCAAA[C/T]GGAAAATTGGGGGGT	9873
rs564950089	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958363	TCTCTATCAAAAACA[G/T]AAAAATTAGCTGGGC	9873
rs564953874	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052553	AATTGTACACTACTG[G/T]TACTACATACTGAAG	9873
rs564960284	snp	A/T	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:73124844	CCCCAAACAAGATAA[A/T]TACAGACACTATACT	9873
rs564965258	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72906483	GCTTTCGGTGTTTTA[C/G]TCATGAAGTCTTTGC	9873
rs564987727	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73059866	ACAATCCTTGACTAA[C/T]AGAAGACTTGATAAA	9873
rs564994910	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999143	ACATTCCCTTCTTGG[C/T]TTAAAGCAGTTTGAA	9873
rs565023485	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944444	TCACAGCCAATATCA[C/T]ACTGAATGGGCAAAA	9873
rs565023936	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72917697	TCAAGACTAGCCTGG[C/T]TAACATGACGAAACC	9873
rs565048747	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067868	CTGCTGATAAAGACA[C/T]ACTCAAGACTGGGTA	9873
rs565057112	in-del	-/AAAAT	0.0019996	0.0315563	intron-variant	FCHSD2	GRCh38.p7	11:73080965	AAAAACAACAAAAAT[-/AAAAT]AAAATAAAATAAAAT	9873
rs565057427	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991554	ATGCAAGGCTGGTTC[A/T]ACATACGCTGATCAA	9873
rs565078733	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72976453	CGTGCTAATTTTTAA[A/G]TTTTTTTGTAGAGAC	9873
rs565088259	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998569	TAATTTGGAACAAGG[A/C]TTGGGGAATAGTAAG	9873
rs565089668	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72884318	CTAGATGTTAGGAAA[C/T]ACATGTTTATTCTTC	9873
rs565095242	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73040303	ATTGTTTCGCAGTCA[A/T]GTGGAAAAACAAAAA	9873
rs565111729	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73068603	AGTTTTATCAGTTTT[C/T]ATACAGTTAACAAAA	9873
rs565113329	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844756	ACAATCTCAAAATGT[A/G]AAATTAACTCCAAGT	9873
rs565117899	in-del	-/A	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73063368	ATCAACACTATGAAG[-/A]AACTGCATCAACTAA	9873
rs565132893	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73100032	CGCTGCCTTCCCTGA[C/T]GCACCCCGGAAGGCG	9873
rs565134858	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73092271	TAGCTGGGACTATAG[A/G]TGTACACCACCACAC	9873
rs565148324	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990979	GCAAGACTAATAAAG[A/G]AGAAAAGAGAGAAGA	9873
rs565171678	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061454	GGAATACCAGTGAGA[C/T]AGAACGATTCACTTC	9873
rs565173024	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837265	CCCCAAATCATGGAG[A/G]AGATTCATTAATGGG	9873
rs565175823	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936888	ATATTAAAAATAGGC[G/T]ATTTAAAATCTTTGT	9873
rs565185548	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838069	CACAGCCTCCTTTCT[A/G]TTAGTCTATGTGATG	9873
rs565192277	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73056258	GGCTTACGAGCCAAG[A/G]TAGGGGTCCTGTGCA	9873
rs565202395	snp	C/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72883519	GGGGGATATATGAAG[C/G]GCTAAAAACTTATAA	9873
rs565217183	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132995	GAAGATATACAAATG[A/G]CCAATAAGCACATGA	9873
rs565235587	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062005	CCTGACCCCTGTTCC[C/T]CCTGACTGGGAGACA	9873
rs565240327	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72876663	TGCAGTGGAGTTCGA[C/T]GAATGCCAATTAGGT	9873
rs565242262	in-del	-/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72901216	GGCAACATGGTGAGA[-/C]CCCCCCCATCTCTAT	9873
rs565245370	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73076980	CCAGGCATGGTGGCG[A/G]GCACCTGTAGTCCCA	9873
rs565265243	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085151	ACGGAAGAAGTTTCA[C/T]CTTAAACCTAAAGAC	9873
rs565268454	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72983738	TTGAAACCATGACAT[A/G]AGTCTCATAAAATAG	9873
rs565287095	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030849	CCTAAAGCCTACTCT[C/T]TCAGCAAAAAATCCT	9873
rs565289889	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73085519	CTCCCTTAATTTTTC[C/T]CTTTTTCCCCTTTTG	9873
rs565304144	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72975599	TCCTTACACATTGTA[C/T]GCATGCATCAAAATA	9873
rs565319093	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72910019	TAGGAAGTGAGGAGC[A/G]CCTCTGCCCGGCCAC	9873
rs565320514	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72978597	GGGGGAGGGTCCCTG[C/T]GGGAGGTGACTGGAT	9873
rs565324719	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914547	AACAGACACATAGAC[C/G]AATGAAACAGAATAG	9873
rs565328033	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73076230	ATAAAGACTAATATG[G/T]TTATTAGGCAGCATT	9873
rs565348220	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73023510	ACATGTATTAGAATG[C/T]TAAATCCAAAAAATT	9873
rs565353750	in-del	-/TTGAT	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72911933	AATGACATTACTTTC[-/TTGAT]TTATTTTTCAGAATG	9873
rs565362249	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961535	TGCTATGATTACAGG[C/T]GTGAGCCACCATACC	9873
rs565377850	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960053	AAAGGAATATGTAAG[C/G]CTGGGTAGTCTATAA	9873
rs565382465	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72946762	ACTCTACTTTTTACA[A/T]CCACCTTTAAGGTAG	9873
rs565383764	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72973179	TCAAGACCAGCCTGA[C/T]CAACATGGAGAAACC	9873
rs565383827	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73016075	TGGGAGGCCAAGGTA[C/G]ACAGATCACTTGAGG	9873
rs565386542	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071169	GCTGCTCTAACTAGC[C/T]AATACCTTCTGTCAT	9873
rs565393826	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976468	ATTTTTTTGTAGAGA[C/T]AAAGTCTCACTATGC	9873
rs565396381	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854264	AGCACAGACTTGAAC[A/C]GATATTTGTAAACAA	9873
rs565404153	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73015701	TCCGAAAACACAGCA[A/G]AGGAAAGAAGTAATT	9873
rs565427402	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132177	ATTTCAGAAATGTAA[G/T]AATGTAAAACAATGT	9873
rs565429550	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959487	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	9873
rs565450938	snp	C/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:72962400	TATAACCTACATCAA[C/T]AAAAGCTCTTTGATT	9873
rs565454670	snp	C/T	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:72906120	TTCCTTTTTAATGAT[C/T]GCCATTCTGTTGTGA	9873
rs565456986	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953712	ACAAAGAAAAGAAAT[A/C]GAGAATGAAGAAAAG	9873
rs565461897	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869905	ACTTTCATAACTCCT[C/G]ACTGTCTACTGAGTA	9873
rs565488161	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139624	AACCCAGTGAGAGCA[C/T]ATAACCATCTGGGGT	9873
rs565489340	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73119271	TCATGCCATTGCATT[C/T]CAGCCTGCACAACAG	9873
rs565526567	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72909096	CTGTTGCCGATACTG[C/T]CGTGATCTCAGCTCG	9873
rs565527812	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72969329	TGGCTTTAAGTTATT[G/T]ATATCAGGAATAAAA	9873
rs565537448	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72903918	ACCAACCATTTATTG[A/T]GAGAGTTTACCAGGT	9873
rs565541067	snp	A/G	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73108793	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT	9873
rs565563165	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72915712	AATCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA	9873
rs565569863	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73053857	AATTGTTTTCTTTTT[C/T]CCTATGTATGACCAT	9873
rs565576568	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73116055	AAATATGATGACTGC[A/G]GATTTTTAAATAAAT	9873
rs565585231	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901590	ACCAAGTTATGACAG[C/T]GCACAGCACTGGAAA	9873
rs565585372	in-del	-/A	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73073635	ACGCTCAATCTTTTT[-/A]AGTCAATCAATCCTT	9873
rs565609111	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73096294	GTCTGTAATCCCAGC[A/G]CTTAGGGAGGCCAAG	9873
rs565609619	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855273	CAAGAGCAAAACTCC[A/G]TCTCAAAAACAAACA	9873
rs565621229	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73086774	CAACTGTACACCAGC[A/C]AATTAGATAAATTAA	9873
rs565632744	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72871058	AAAGTTCCTATTCTC[C/T]AAATTCAAGAAAGGG	9873
rs565636660	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73013302	TAGAATTTCTTTTAC[C/T]AAACTGTCTGCCTGG	9873
rs565645939	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062971	CAAGAAGAGCAACCC[C/T]AAGACACATAATCGT	9873
rs565657372	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72911955	ATTTTTCAGAATGCT[C/T]ACTGTTCACATATAG	9873
rs565661698	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841394	TTTTTGCCCTTCAGG[C/T]GAATATGTAGGTTTC	9873
rs565681788	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017311	TAGGAATATATGTGG[G/T]CCCCTAACACTATAA	9873
rs565713250	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72987976	AGAAATATTAAATGT[A/G]TTTTCCTGTAACATC	9873
rs565730132	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916114	ATAACTAATGGGTAC[C/T]AGGCTTAATACGTGG	9873
rs565740221	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72863754	GATCAACATTATCAG[A/G]GAAATGGAAATTAAA	9873
rs565746256	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009947	GGATGTCTAAATCTC[G/T]TTAGACTTGGGAAGT	9873
rs565746385	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018355	TGGGTCTTACTATTT[A/G]TGTCTTTTTCTAAAA	9873
rs565748781	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002373	TGTGTTGCACCAGCA[A/G]AAACTGTCAGCATAA	9873
rs565775561	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72946977	CAGCCATCTATGCAA[C/T]AGCTCACCCAGCTAC	9873
rs565780006	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983016	ATAAAAGAAAGGGGC[C/T]GGGCGCGGTGGCTCA	9873
rs565794161	snp	C/T			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72844198	TTTGGGAAGCAAAGG[C/T]AAACGAGAAGGCACT	9873
rs565799572	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72988843	ATATAACACATGTAG[C/G]TCAAATGAAACCACC	9873
rs565808062	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72961045	GTAACACACATGTGA[G/T]GCTGCCTTAGCACTG	9873
rs565809219	in-del	-/GAG			intron-variant	FCHSD2	GRCh38.p7	11:72904366	TGTTTTGTTCCTCTT[-/GAG]GAGGAGATTTCAACC	9873
rs565814250	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940452	CAATAAATAGTAAAT[A/C]AGCTATTTTCCTTTC	9873
rs565828083	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902980	AGATAAGGAAACACA[C/T]TGGTCTTTGCCATCT	9873
rs565853751	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855901	TCTATACTCTTTGAA[C/T]TATTAGAATATGCAC	9873
rs565855051	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72873293	GAGATCGCGCCACTG[A/C]ACTCCAGCCCAGGCA	9873
rs565861632	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72846438	GCCCGCCTTGGCCCC[A/G]CAACGTGCTGGGATT	9873
rs565865774	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73121374	ACACAGATGAAGGAC[A/G]CTTAAAAAGGAAAAA	9873
rs565873855	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73111222	AGAGTGATGTTTCTT[C/T]GCTGATTTTCTGTTT	9873
rs565877440	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73130650	GTATTACCAAAACCC[C/T]AATTCTTTCAATTTC	9873
rs565889221	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72873955	AGGATACTACCGTGC[C/T]ACTTTAACCAATCAA	9873
rs565901673	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73056683	AGGTAGAGAAGAGAG[A/C]ATAACAGAACAATAA	9873
rs565910593	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047222	ACCCATATTATTTGA[A/G]TTGTTAAAACTACCA	9873
rs565926075	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72880912	AACAACAAACAAACA[A/C]CCACACTATAGAACT	9873
rs565935959	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088786	AGTTCACACTTTCAC[C/T]ATTTAAAAACCTCTA	9873
rs565936733	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138301	ACACAAACTCAGGAC[G/T]GTCTGACTGCAGTGT	9873
rs565940864	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72865743	TGAGATTCTGGAGTT[C/G]GTGGGGGTGGGGAGT	9873
rs565941079	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72947955	AATGGTATAATCTTA[C/T]ACAACATAATTTTTA	9873
rs565945731	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72904318	GATCACCTCTCTAGT[C/T]GCCAAACTTGTCCTC	9873
rs565957471	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73124382	ACCTGCACATTGTGC[A/C]CATGTACCCTAGAAC	9873
rs565958524	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73034248	CTCCCTCCCCTTTAA[A/G]GTTTTTCTTTAAATA	9873
rs565977644	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73033050	TCCCAGCACTTTGGG[A/G]GGCTGAGGCATGCGG	9873
rs565997531	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72870050	TTGCTGTTCCTCTGA[C/T]CCATCATGTGCTTGC	9873
rs565999722	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137752	CAGCATACACAGGGG[C/T]ATGAATGTAGAGTGC	9873
rs566001330	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73081113	TATTTTACATTTTAA[A/G]TAATAAACATGTCCT	9873
rs566001700	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73093381	GGGACCCACAAAATT[G/T]CAAGTCGTGTCAGAA	9873
rs566029766	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940944	AAATCCTGACACCCA[A/G]TGGATCACCAAAGCA	9873
rs566032492	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73112464	ATTAAATGCCTTAAG[A/G]TAGTCTTCTTTGGGC	9873
rs566038300	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083500	GTTGCAGTGAGCCAA[G/T]ATTGCGCCACTGTAC	9873
rs566042940	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971060	GATAAGTTATCCCTA[C/T]TGACCCCCCTGCCCA	9873
rs566044513	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932951	TGATGTTACATAACA[C/T]TTATAAAATCGTATA	9873
rs566056230	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72888452	AAGTGGGAGGTGAGA[C/T]TCTATAGATAATAAG	9873
rs566068447	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73116750	GCCATGTTGCCCAGG[C/G]TAGTCTCGAACTCCT	9873
rs566079071	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72990168	GTGAAGGAAAAGGTT[-/A]AAAAAAACACAAAAT	9873
rs566080150	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905445	CCAATTATACTTTTT[A/T]ATTTTTATTATACTT	9873
rs566082682	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115847	ATTGAGGGTAGCCTC[C/T]TTTACTTAAAGTCAA	9873
rs566095515	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041962	AGACAGAGTCTCACT[C/G]GTCACCCAGGTTGGA	9873
rs566101422	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73079959	TACATTATTATATAG[C/G]ATTGTATAAACAAAA	9873
rs566123665	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73089602	AATGTTATTCAGCCA[A/T]AAGAAAGAATGAAGT	9873
rs566128530	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991132	ACTGATAAATTCCTC[A/G]ACACATACACCCTCC	9873
rs566131241	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72963618	GGAAGATAATTTTTC[C/T]ACAGATGGGTAGGGT	9873
rs566137681	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72977132	ATTTCACCATATTGG[A/C]CAGGTGGTCTTGAAC	9873
rs566140375	in-del	-/A	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72977488	AAACAACTCTATAGG[-/A]AAAAAAAAATCTAAT	9873
rs566146045	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123026	TCCCATCAAAAAAAA[A/C]CACAAAATAATTAAT	9873
rs566146128	snp	A/C	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73034884	TGTCTGTCAACAACA[A/C]AACTGAAAATCCTCT	9873
rs566149347	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119959	TTACAGTTCCACATG[A/G]CTGGGGAAGCCTCAC	9873
rs566168842	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72934095	GCCTGGGCAACAGAG[G/T]AAGACACTGTCTCAG	9873
rs566188784	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081845	AAATACTCAGAGCAT[A/G]GTACAAAGTAAGGAT	9873
rs566199903	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072058	GACCAGGTAAACAAC[A/C]AATGAGTGAAGACAT	9873
rs566205567	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027786	TGCTGCTCTGTGCAG[C/T]CTTGGGACACGGTGC	9873
rs566213888	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72926934	AGAGTGAAAAAAATG[A/G]CGACTTGGTGCACTA	9873
rs566251767	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971597	AGCACCTCTAGGAGC[C/T]GAGAATGACCCCAGC	9873
rs566254652	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057766	TTTAAATCAGAGCTT[C/T]CCAAACAATGTATTG	9873
rs566257098	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72965069	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT	9873
rs566264426	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072611	AACAGGACACAGAAA[A/G]TAATACTCAATTTTG	9873
rs566269176	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73003775	ACAGGCGTAAAAATT[C/T]TATTTCACCAGGTTT	9873
rs566278179	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73127121	TTATCACTAAAATAC[A/C]ATCAGGAGACATATA	9873
rs566284323	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72877407	AATGGAAATATCACT[A/G]AGTATAGTCTTGTTC	9873
rs566323890	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064877	TTAATAGCCTACCAA[C/T]TAAAAAAAGTCCAGG	9873
rs566325813	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73073580	CTTCACAATATTTTT[C/T]TTTTAGGATGGCTCA	9873
rs566351352	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023664	ACAATCATGTTCTAG[A/G]TATTTGGCCAACTGA	9873
rs566372738	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73048783	AGGGATGTATGTATA[A/G]TTCACCTCAAGAGAA	9873
rs566393403	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956135	ATGGAGCAATTTGAG[C/G]GTAAAAATAAATAGT	9873
rs566406976	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093295	TTAGCTATAATAAAT[A/C]ATAACCTTACTGAGT	9873
rs566418113	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105387	TACAGTACACCCTCT[A/G]TATAAGACACCACCA	9873
rs566420416	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113000	TACTTTCTAGATCTG[A/G]TAGGCGTGCTTCATT	9873
rs566431974	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73044273	CAATTAAAAAAAAAC[C/T]TATGAATATTTCCAA	9873
rs566438305	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936313	TATGTACTTGAGCAG[C/T]AGAACTGCTCTAAGT	9873
rs566468563	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73085329	CCAGGAATCTGACTC[C/T]CAGGCTAGGTAACAA	9873
rs566478037	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016610	GCAGCCAAACTCTCA[A/T]ATACCAGGAAAGAGA	9873
rs566499344	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73005608	TCTAACTACATTCAC[G/T]CTGTTGAAAATTGTT	9873
rs566507392	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901106	TTAAACAATTGCCAA[C/T]TGGGGCCGGACATCG	9873
rs566540582	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73107847	TTTATCCATTTATCT[A/G]CTGATGGACACTCAG	9873
rs566558413	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030082	TAGGTAAGAAATACC[C/T]AAGGGAATGCCATTA	9873
rs566573282	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72965036	CCTCATGATCCGCCC[A/G]CCTTGGCCTCCAAAA	9873
rs566579881	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967642	ATGACAGCCAATGGG[C/G]TATAGAGCTTTTTTG	9873
rs566591143	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075688	GGAGTGGTGGTGCGT[C/G]CCTGTAATCCCAGCT	9873
rs566591431	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901855	TATTCCATTTATTAA[C/T]TCTATTCTGGTTTTT	9873
rs566602321	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72914244	GATCTTGAACTCCTG[A/G]CCTAAAGTGATCTGC	9873
rs566634366	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962296	GTGATGATGCAATCG[C/T]TCTGACAGCTAATGA	9873
rs566643733	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72902028	TACAGGGGCCCACGA[C/G]CAAGCCCAGCTAATT	9873
rs566651688	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72847733	AGTCTCGCTCTGTCA[C/T]CCAGGCTGGAGCGCA	9873
rs566653074	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076580	CAGGAGATGAACTGG[A/T]ATAATGGCAATGTTC	9873
rs566654419	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72937074	ATCCAATAGCAAAGA[A/G]GAGTTCTTCCTTAGC	9873
rs566656215	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72868821	ATATTCTCAAGGCTT[A/T]GTCCACATGCAGACA	9873
rs566667686	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134979	CCTCCCAAGTAGCTA[C/G]AGTAGCTAGGATTAT	9873
rs566669736	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860688	CATCTCTACTAAATA[C/T]ACAAAATTTAGCTGG	9873
rs566679120	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73045995	TTTCAGTAATTTTTT[C/T]TTTTTTTTTTTTAGA	9873
rs566680872	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73039082	AATTGCAGAATCACT[A/G]TTTATTTTTATCTGC	9873
rs566689812	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141789	GGGGAAGGGGCGCAG[A/C]GGTCGCCCCAGCCGC	9873
rs566718093	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72934822	CCAAACTTTTTGACT[A/G]TTGGACACAAATTTC	9873
rs566719135	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72879930	GTTGAACCCAGGAGG[C/T]GGAGCTTGACGTGAG	9873
rs566724549	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061562	TAAGATCCACTGGCT[G/T]GAAATTCTCACTGCC	9873
rs566725245	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73103151	GATGGAAATGTTCTA[C/T]ATATTGAGTGTAGTA	9873
rs566733545	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142161	GGAGACGGCGAGGGG[A/G]CGGGGGCCCCAGGAG	9873
rs566767993	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061203	CTCACCTGGGAAGCA[C/T]AAAGGGTCAGGGAAT	9873
rs566779153	snp	A/C	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73068980	TGACTTCGCCACTGC[A/C]CTCTAGCCTGATGAC	9873
rs566786272	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73053944	TATTTTTTACTCATC[C/T]AATAATTCACTTTTA	9873
rs566827853	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72929340	TATCTTTTTCAGCTA[C/T]CCAACACCCAGAATT	9873
rs566827994	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72960223	GGAGGGGAGATGCCA[C/T]GGCCAGTCTCATGTG	9873
rs566829487	snp	A/G	0.0275645	0.114116	intron-variant	FCHSD2	GRCh38.p7	11:72945549	CCAAAATTGACAAAT[A/G]GGATCTAATTAAACT	9873
rs566843134	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72862131	CTTTAACATGATAAA[C/G]GGCATCTACAAAAAC	9873
rs566857310	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893615	CCACTATGCCCAGCC[A/C]AATATTTTTCCTTTA	9873
rs566870342	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999670	ATTCAGGTCTGAGAT[C/T]ACTTCATCAATGGAA	9873
rs566896594	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72944956	GGAAGAATCAATATC[A/G]TGAAAATGGCCATAC	9873
rs566906653	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72854441	TCTACCTATCTGTCT[A/G]TCTGGTTAGAGACAG	9873
rs566913373	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72905520	GGTATACATGTGCCA[C/T]GCTGGTTTGCTGCAC	9873
rs566914526	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838406	GATGAGAATCTTTGC[C/T]ACATCCTTGTGGTCA	9873
rs566915416	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938698	TTTTACTCGTATTCT[A/G]CACAAACAGTAGAGA	9873
rs566919751	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846154	TCCCAGACTACTCAT[A/G]ATGAGTAAGCTGCTC	9873
rs566922829	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892898	TGTGAGCCACCGTGC[A/G]TGGCTGGTAATTTTT	9873
rs566932580	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72861635	CAGTTCCAATCAATA[C/T]ATAGAAAGGATAGGC	9873
rs566947150	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73094876	AAAATATTTTTTAAC[A/G]AGGCAAGCGGAACGA	9873
rs566955209	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72930670	GAATTGCTAGAACCT[A/G]GGAGGGAGGCTACAG	9873
rs566966443	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73057634	CATTAGGCTCCATTT[C/T]CCTTTCAACATCAGT	9873
rs566986544	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72884100	TTAAGAGACCACTCT[C/T]AGTATCATTAATAGC	9873
rs567007364	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72993455	CTATAGAGACACATG[C/T]ACACATATGTTTATT	9873
rs567014258	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009604	TGATGAATTCCCTAA[C/T]CTTTTGCTTGTCTGG	9873
rs567018117	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73045469	AAGACACATGCACAC[G/T]TATGTTTATTGTGGC	9873
rs567023060	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72997753	TCATCCAGGCTGGAG[G/T]GCAGTGGCACGATCT	9873
rs567028729	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73048941	CTCATTGCTATCAAA[A/T]TCTCACATGACAAAG	9873
rs567043121	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73139715	GTGTAAAACCGTTAA[A/G]GTCAATAAAATGATT	9873
rs567048318	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72985534	GAGGCAAGCGTCAGC[A/C]AACTTTCAGGGCTGT	9873
rs567054922	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977926	CCCAAATGCCCATCA[A/G]TGATAGACTGGATTA	9873
rs567064875	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73085632	AAGGTGCAGGTTCAC[-/A]AAAAGACTTCAGAAG	9873
rs567068757	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72993973	TCTGTGAGTACGGTG[C/T]ATCCGGACATGTCCC	9873
rs567084267	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886402	ATCTGCCAGCATTCA[C/T]CTTAAGTCTTCTTCT	9873
rs567093725	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025392	ACGAATGCAGGAAAA[G/T]AAAACCAAATACCAC	9873
rs567103811	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955152	ACTTCAGATGCTAAT[C/T]GGAAGTCTCAGGTTG	9873
rs567119080	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977236	CCAAAACTATTAAAA[C/T]AAAGCATTGGGGGAA	9873
rs567124578	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141714	CGCGCCCCCCACCTG[C/G]AGCCGGCGGCAAGTC	9873
rs567135380	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117430	ATATTTTGGGTTTTT[C/T]CCTAATTTATTGAGA	9873
rs567136720	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934231	CTTGTCTAGCATTTT[A/G]CATTTAAATGAGCAA	9873
rs567153505	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923488	TGGTATTTTTTTTTT[A/T]AATTATGAAAGCCAT	9873
rs567154980	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042550	ATTGAGGTCTTCTGC[A/G]GTTCCATACAATTTT	9873
rs567158003	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72891944	TTACTTGAAACAAAA[A/G]TTTTCTTATTACTGT	9873
rs567158451	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73002926	GAAAGCTCCATGAAG[A/G]CAGGGGTGTATGTCT	9873
rs567166673	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118798	AACTCTGAGAGACCA[C/T]TATTACCATTTCTGT	9873
rs567182418	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73136511	GAGATCACACCACTG[A/C]ATTCCAGCCTGGGCA	9873
rs567187743	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72878980	CTGGTTTTGGTGGCG[G/T]GCACCTGTAATCCCA	9873
rs567222266	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935245	GAATTAGGAGGGAAA[A/G]TGGGTCATTTTCCTA	9873
rs567226003	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73070821	ATAACTAACCAACAC[C/T]TCAGTGGTTAGTTAA	9873
rs567229865	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73126116	GGAGGCCGAGGTGGG[C/T]GGATCACAAGGTCAG	9873
rs567230833	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72964270	GGTTGATGGTTCCAA[C/T]CTTATGTTCTCATCA	9873
rs567259543	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73107583	CATCCTCACTTCCCA[C/G]AAACACACACCCTCA	9873
rs567261887	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73012256	ACTCCTTAAGTGTGT[C/G]GGCGGGGAGCAAGGG	9873
rs567271702	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857526	TCATTGCAACCTCTG[C/T]CTCTTGGGTTCAAGC	9873
rs567272649	in-del	-/T	0.299487	0.245053	intron-variant	FCHSD2	GRCh38.p7	11:73110155	TAGTTTTCTTCTTTT[-/T]TTTTTTGATGTGTCT	9873
rs567285006	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73097662	CAATCCCTTCACTTG[C/T]TATTGAGAATTTCTA	9873
rs567301100	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956017	TTGGGGAAATAGTTG[A/G]TTCCAGAATTGGGGC	9873
rs567306163	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72896248	TGAAGATCTTGTTAT[C/T]TGCTGTTCAAAGAAG	9873
rs567318659	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72849557	GATTTGGGGAAAAAA[A/G]GAGTTCTAGGCAGAC	9873
rs567319292	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042138	CACTGTGTTGGCCAG[G/T]CTGGTCTTCAACTCC	9873
rs567338214	in-del	-/C	0.00018615	0.00964575	intron-variant	FCHSD2	GRCh38.p7	11:72902669	ATATCTTTAGGTCTT[-/C]TAATGAGGTTAAAAT	9873
rs567349751	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73090172	TGTAAACCATCTTTT[C/T]ATATAAAAATGTTTA	9873
rs567374565	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889501	TAATGCTTGAGCAAA[A/G]GAGTTTGAGACCAGC	9873
rs567382720	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035118	ACTCCTGGACCTTGA[C/G]AAGTTATTTAACTTG	9873
rs567394774	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73096016	CCTAAAGTGCTATAG[-/A]AAAAAAACAAAAAAC	9873
rs567403889	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72996603	ATAATTGTAATACAA[C/T]TGTGTTTATCTTCCA	9873
rs567404209	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105929	TAAATAAGATACCTA[C/T]AGAAGATACCTGGCA	9873
rs567410686	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117977	ATATATACATTTTCT[A/G]AGTTTTGACAAATGT	9873
rs567413586	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980771	ATGTGTATGTATATA[C/T]ATACATCTCACTCTC	9873
rs567415775	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73039545	AAAGAAAGAAAAGAA[A/G]TATTAATATGTCACA	9873
rs567435333	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72957015	AGAATCAAAGGACTC[C/T]AGTCTTTTTTTTTTT	9873
rs567437698	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927135	GGTAGGCAAAAAACC[A/C]TGTAAGCCTTTAAGG	9873
rs567439167	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965688	CATTTCCAACACCTC[A/G]GAAGGCACTCTTTCC	9873
rs567442668	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72889228	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG	9873
rs567447118	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988906	ATAGAGAACAAACTA[C/T]TAGCAACAATAACAT	9873
rs567455114	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72870230	AATTCCTTTTTCTCT[A/G]CTCCTAAAGCACTCT	9873
rs567455954	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72873258	CGCTTGAACCTGGGA[A/G]GTGGAGGCTGCAGTG	9873
rs567473434	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73117356	CCACACTCTTAAATA[C/T]TACATAATAATGCAT	9873
rs567473486	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72957939	TGGAATTATATAAAC[A/T]TAAATTATTTTAAAA	9873
rs567474713	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73113290	AAGGTCACATAGCTC[C/T]GTTTCTCCAGGACTG	9873
rs567479069	in-del	-/T/TTTTT	0.481396	0.0946345	intron-variant	FCHSD2	GRCh38.p7	11:72959220	ATATATCCAGCAGTC[-/T/TTTTT]TTTTTTTTTTTTTTT	9873
rs567515127	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72905009	AACGTTTACTTCCAT[C/T]AGGAAGCTTGCTTCT	9873
rs567533197	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72914540	CTAGTACAACAGACA[C/T]ATAGACCAATGAAAC	9873
rs567548673	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035377	TCTCATCATGTTGCC[C/T]GGCTGTTCTCGAACT	9873
rs567555025	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72981371	CTTTAACTTCCTCTT[C/T]GCTTTAGGCAGAGAG	9873
rs567568513	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72851669	AATTGCTTGAACCTG[A/G]GAGGCAGAGGTTGCA	9873
rs567576985	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927491	ATGTAGGGGAAGGGA[A/G]TGTAAGGGAAATCTC	9873
rs567580206	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844436	GTGGAGACTGAGCTG[A/C]TCCATTTGCGTGCTA	9873
rs567581964	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72973574	CAACACTATCTATTG[G/T]CAGAGTGGTAGTTAC	9873
rs567590743	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73107320	CCCAAAGTGCTGAGA[C/T]TACAGGCATGAGCTA	9873
rs567590868	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998314	GGAGGCTGAGGCAGG[C/G]AGATCACTTGAGGTC	9873
rs567600269	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73065967	CTATCCCCATCAAGC[C/T]ACCACTGACTTTCTT	9873
rs567606445	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72919552	AATTTCCTCCATATA[A/C]AATGAACATGGTAAT	9873
rs567616666	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875216	TCAATAATGGTAGAT[A/G]ATAGTATTTGCTACT	9873
rs567624753	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73139192	TTTATCATTAACACC[A/G]GAGTTAATATTTTTC	9873
rs567640456	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73013435	TGGCTATCTCCTGTA[G/T]GCTTACAAAGGACAG	9873
rs567641221	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72845051	CCTAAAAAGTATCAA[C/T]ACGACCAGACGTTAA	9873
rs567644795	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72972459	GGAAAGTAGAGGATG[A/T]CACAGGCAGGTATAG	9873
rs567659452	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990693	ATACCAGAATCTCTG[C/G]GACACATTCAAAGCA	9873
rs567661276	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72866828	AATTTTCGTCAGTTT[C/T]GCTAGCAAGCCTGCC	9873
rs567665031	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72918717	TTTCAAATAAATGTA[A/G]AATAACATTGTTATT	9873
rs567683460	snp	A/G			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140402	GTCATTCCATTTCAT[A/G]CACAAGCTCAATCCA	9873
rs567687572	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73021165	TAAAGGTGCAGGCCA[A/C]TGTGTCTGGCCTATC	9873
rs567707252	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087017	AACTGTAAAACAGCC[A/T]CAGGCAGTTCCTTCA	9873
rs567709290	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73077747	TTAATGCTAAATGAA[A/G]AAGCCAGCTGGGAGA	9873
rs567723950	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72858533	CAGAAGACCAAATAC[C/T]GCAAATTCTCATTTG	9873
rs567746821	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72859361	ATTTAGTGGCCATCT[C/T]GGTTATCCCAATTGA	9873
rs567772902	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73106289	ACATAAACCTATATC[C/T]CCAGCATTCGGGAGG	9873
rs567798628	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913030	AGCAGCTTTGTCTTA[C/T]GTGGCAGGAGCAGGA	9873
rs567808812	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014371	TTGCCTCAAGTGATC[C/T]TTCCACCTCGGCCTC	9873
rs567814300	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73048982	AACAGTAAATATTTA[A/T]ATAACAGAATCAAGA	9873
rs567816148	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059322	AGGATTTTTACACTA[C/T]AAAGTTGTTTCCTTT	9873
rs567817244	in-del	-/AAACAAAC	0.00239568	0.0345268	intron-variant	FCHSD2	GRCh38.p7	11:72855280	AAAACTCCGTCTCAA[-/AAACAAAC]AAACAAACAAACAAA	9873
rs567836027	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960736	AATGTTGGGAGTTGA[G/T]GTGGAGAAAGGGTAT	9873
rs567836053	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969284	TTCTCCCTCTTGGAT[C/T]ATGTTAGAATGGTTT	9873
rs567840977	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951330	GTGATGAAACAGATG[C/T]TGCAGATTGGGAAGC	9873
rs567841954	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862299	ATAGGAAAGGAATAA[A/G]TAAAACTGTCTTTAT	9873
rs567857546	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73107239	TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC	9873
rs567870649	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900209	CCTTCATTAACATGC[A/C]AACCCACACTTCCCA	9873
rs567872270	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961463	GTCTCACTATGTTGC[C/T]CAGGCTGATATTGAA	9873
rs567889543	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950693	AATTTGTAGTTTTTC[C/T]TTATTTCTTTTAGGA	9873
rs567899426	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998718	ATAAAAAATATTAGA[C/T]TGCTTAATATCACCA	9873
rs567899906	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73075796	AGACTGTCTCAAAAG[-/A]AAAAAAAAAAATCAA	9873
rs567901134	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72959396	ACCATGCCCGGCTAT[-/T]TTTTTTTTTTTTGTA	9873
rs567904713	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72854564	AGCCCCCCGAGTAGC[C/T]GGGACTACAGGAACA	9873
rs567917668	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72855112	AACCCTGTCTCTACT[A/G]AAAATACAAAATTAG	9873
rs567924014	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943537	TATTAATAGCTTTAA[C/T]GAAAGGGAAGGAAAT	9873
rs567925198	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73109861	CTTTTATTGTGTTGA[A/G]GTATGTTCCTTCTAT	9873
rs567953165	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043391	TGGGCAACCTGTCAA[C/G]TAATGTATAATTTAA	9873
rs567954294	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890507	TGCTCTTTCTCCAGG[C/T]TTCATATGAAAGATA	9873
rs567954753	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052075	CACAGAACAAAGAAA[G/T]TTAGTGACATGTTTT	9873
rs567957759	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977128	CAGCATTTCACCATA[C/T]TGGCCAGGTGGTCTT	9873
rs567970972	in-del	-/A	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73069822	ACTCTGGGTACCAGC[-/A]AGGCAAATAAAACAT	9873
rs567976151	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870275	ACAATGTGATAGGCA[C/T]GAAATTATACTTAGC	9873
rs567983893	snp	A/C/G			intron-variant	FCHSD2	GRCh38.p7	11:73099134	GGTAGAAGAATCACC[A/C/G]AGCCCAGGCGTTCCA	9873
rs567987376	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73131660	AGTAAGCCAAGATCG[C/T]ACCACTGCACTCCGG	9873
rs567988608	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110417	CAAGGTTCAATCTTG[A/G]TAAGTTGTATGTGTC	9873
rs567991949	snp	A/G			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144432	AGGCAGGAGAATAGC[A/G]TGAACCCGGGAGGTG	9873
rs567997984	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73139818	GGTCCTTGTTTTTTC[A/T]GAATACTATGTGTGC	9873
rs568002697	snp	C/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72940412	AAGGAAATAATATAT[C/G]TAATGAGGTTAGTAT	9873
rs568016320	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73066548	AAACTATCATCAGAG[C/T]GAACAGGCAACCTAC	9873
rs568018249	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73033207	GCAGGAGAATGGCAT[-/A]AACCCGGGAGGCGGA	9873
rs568020525	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031826	TTTTCGCCTGGAAAA[A/G]GCATATGCATTGCTT	9873
rs568045108	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73002294	TATACCAGATGAATC[A/G]GTTTAGATGGAAATA	9873
rs568080041	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72977738	GGTGGGACTGTAAAC[C/T]AGTTCAACCATTGGG	9873
rs568082796	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73062978	AGCAACCCTAAGACA[C/G]ATAATCGTCAGATTC	9873
rs568102557	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73069517	TGATCACTAACAAAG[A/C]AATGGATAAGATAAA	9873
rs568117260	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72915059	TACAAGAAAGAAACA[A/G]ACAACTTCATTCAAA	9873
rs568129260	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73096885	CTGAGTCTTTTTATC[A/T]TGAAAGAGTGTTAAA	9873
rs568129286	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016858	AAACAGAATGTTTAT[A/C]TATAACAGGTGTCAG	9873
rs568143852	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062327	AAATCCACAAAGATG[A/G]GGAGAAAGCAGTGCA	9873
rs568144352	snp	A/T	9.88468e-05	0.00702948	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72887505	CTCTAGCTTCATCTA[A/T]TTTCTGTTCTAGCTC	9873
rs568147690	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73025242	TGGAATCAACCTAAA[C/T]GCCCATCAGTGATAG	9873
rs568171656	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870967	TGACTAACTTGTTTG[C/T]TGACTAACAGTAATG	9873
rs568177923	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73132460	AGCAGAGCTGGGTTT[A/C]AATCTACGGCCTACC	9873
rs568202185	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73113960	CTCTTTGCTCAAGGG[C/T]CTAGGGCTCTACAAT	9873
rs568202674	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915684	TTAGCCGGGCGCGGT[C/G]GTGGGCGCCTATAAT	9873
rs568203042	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909088	GTCTCCCTCTGTTGC[C/T]GATACTGCCGTGATC	9873
rs568211674	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72953618	CAGGTACTGGAGACA[C/T]TGCATGGGGGAAAAA	9873
rs568248911	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946141	GGAAAGACTTGGAAC[C/T]AACCCAAATGTCCAA	9873
rs568262463	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73120660	TTTCATCTTGGAAGG[C/T]GGAGGCTGCAGTGAG	9873
rs568272351	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73026510	TAAAATAAAAGAAAC[C/T]GAGTATAAAAATAAT	9873
rs568278979	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72999390	AGTGGCACGATCTCA[A/G]CTCACTGCAATCTCC	9873
rs568317151	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010347	ATTTTCTTGTATCTC[A/C]TTGAGCTTCTTTAAT	9873
rs568317288	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102742	CCATGTGATAATGCA[G/T]CAAGAGCTTCCTCAC	9873
rs568331375	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72954304	GCCTCAAACACCTGG[A/G]CTCATGCAATTCTCT	9873
rs568334904	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027332	GCTTTAACAGAGAGA[C/T]TGGCAGCATTTTGCC	9873
rs568342491	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840099	CTCCAGCCTCCTAAT[C/T]GCTCCCTATATCCTT	9873
rs568343620	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129201	TAAATTGATGTTCTC[A/G]ATTACAAAACAAATT	9873
rs568347660	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72903514	GTGAGCTACCGCGCC[C/T]GGCCTGGAATTTCTA	9873
rs568348214	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73018423	TCTGGCCCTCTCACA[C/T]AACTCTATTTATGCA	9873
rs568358276	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73035782	CTGGAGTACAGTGGC[A/G]CGATCTTGGCTCACT	9873
rs568367513	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055506	AATAAGACAAAGTTT[C/T]AAACCTTGAGATACA	9873
rs568396475	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040742	GGAAATATTTCAAAT[C/T]ATGTATTCTAATTAT	9873
rs568401680	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019116	ATCTAAATGACATGA[C/T]AGTGACTTTTTCAGT	9873
rs568416964	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72946906	GATGTAGGACAAAAA[C/T]GACTGCCTGCCAACA	9873
rs568428887	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72987167	GTGTGCATCTCCACA[C/T]CATCTATCAAATCAT	9873
rs568435769	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047072	TATAAAAGACAAGAT[A/G]CAGAATAAATGTGAA	9873
rs568439706	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939587	GGAAATCTATGAAGA[C/T]GGTTGATGGCTCTTT	9873
rs568455477	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025149	CTGGGTACATACCCA[A/G]AGGAATATAAATCAT	9873
rs568457091	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033348	GGAGGCTACCACTCT[A/G]GTCCTGTCCAAAGAT	9873
rs568458888	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019926	AAAGTTTTTAAAAAA[A/T]TTTTTTTCAAATCAT	9873
rs568468753	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135856	TCGAAATTCCAAAAG[A/G]TAAGAACTGGGGATT	9873
rs568474173	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72940238	CACAATATCTAAATG[C/G]GGCTTTGTGTGTTTA	9873
rs568480826	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840651	AGCCATCATCTTGCA[A/T]TCTCACTGTGGCTCA	9873
rs568498330	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889703	GGGTGACAGAGCAAG[A/C]CTCTTGTCTCAAATA	9873
rs568508727	snp	A/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843138	ATAAAGAGTGCCTTG[A/T]TTCAGTCTTTACCAC	9873
rs568533480	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73130787	GACCATAATATGGAA[G/T]TATATATTTACATTT	9873
rs568537387	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041101	TTCCATTGTGTATAT[A/G]AACCATATTTTCTTT	9873
rs568546650	in-del	-/ATATATATAAAAGATCATATAT			intron-variant	FCHSD2	GRCh38.p7	11:72884569	TTTATATATATGATG[-/ATATATATAAAAGATCATATAT]ATATATATAAAAGAT	9873
rs568565328	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72932866	CAACAAATAATAACA[A/C]CAATCAGAATTCGCA	9873
rs568571374	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73125427	TGCATGGTGTAGATC[A/G]AGTGTGGTGGCTCAT	9873
rs568572903	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72863908	ATGGTATAACCACTT[C/T]GGAAAACAGTTTGTC	9873
rs568579159	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73130165	AGGTGTGAGCCACCG[C/T]GCCTGGCCCATAATC	9873
rs568583775	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890363	GAGTAAAGAATCATT[A/G]AAGAGAAGTAAGAAC	9873
rs568590032	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080131	TAGTAAGACCCTGTC[C/T]CTACAAAATAAAAAT	9873
rs568598083	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113146	CAACTCCAGAATTTC[C/T]GCTTGATTTTTTGTA	9873
rs568598657	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73034013	AGACAATTTTAATAC[C/T]GATAGCAAATATATC	9873
rs568609871	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73102600	CCATTATAACAGTAT[C/T]ACAAGCTGAGACTTT	9873
rs568631298	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72979960	AATGTCCAGGAAATA[C/T]GAAAAGAACATAAAA	9873
rs568652478	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72920240	GTCTGGTCAAAATAA[A/G]ACAGAGGGCACACAC	9873
rs568653574	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925629	CAATAAAACATATAT[C/T]ATCTCATCATGAGAT	9873
rs568659374	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120030	GCAGAAGGCAAAGAG[A/G]GAATGAGGAAGATGC	9873
rs568665491	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846510	AAAGGCTCTCTGAGC[A/G]TCCCCATAACACTGA	9873
rs568673291	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029260	ACAAGACTATTGTAG[A/G]AGCAAATTCTGAGAA	9873
rs568708635	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72883693	TCCCAGCACTCTGGG[C/T]GGCCAAGGCAGGCAG	9873
rs568710473	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864793	TTGGTATGGCTTTTG[A/C]ATAAGAGAAGCAGGA	9873
rs568711460	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73039093	CACTGTTTATTTTTA[C/T]CTGCAACCAGTTTCA	9873
rs568714503	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72980305	TGAAACTGCTGCACT[A/G]GTTTCTCTATTAATT	9873
rs568719740	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72916948	TGAGGTAAGGGTTCA[C/G]AACTTCATTGAACTT	9873
rs568720079	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72961524	GCCTCCTAAAGTGCT[A/T]TGATTACAGGCGTGA	9873
rs568727293	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72920066	AATATAGGATCTAAA[C/T]AGAAAAAGAAGCTTG	9873
rs568760307	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112289	TAAAAGATTTCCCCT[C/T]TGGCACTTTAAACAT	9873
rs568775607	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73070382	AGAACCTAGCATCAC[A/G]CCAGTCGTAAAGTAG	9873
rs568782674	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72956161	ATAGTAAGAGTAACA[A/C]ATTTCAATCCATTGA	9873
rs568786982	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73072427	TTTAATGAAGTTTTT[A/T]AAAACTTCCTTTAAT	9873
rs568796700	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023047	GAGTTACACAAAAAT[C/T]GGCTCAAAATGATTC	9873
rs568802203	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844270	CAGTGAAAATGCAAA[G/T]AACTATGTACGTGAA	9873
rs568805338	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72890436	CTGCCCCAAGGCAGA[C/T]GGAACTCTTTAGAGG	9873
rs568817586	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111588	TTGATTGAAGAGTTT[A/C]ATCCATTTACATTCA	9873
rs568824813	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099667	CCCTGAGCAGTCAGG[C/T]GTTAGGCTTAGCGGC	9873
rs568832686	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73058114	TCGATCTCCTGACCT[C/G]GTGCTCCGCCTGCCT	9873
rs568841510	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942708	AAACATGCTATAGAA[C/T]GTTATGGTATATGCT	9873
rs568847706	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72936607	TAGCAAGACTCCATC[A/T]CTAATTTAGAAAAGA	9873
rs568859249	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044174	TAAATCAAACAAAGA[G/T]ACCATTTTAATAGAT	9873
rs568875975	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72991029	AAATGATAAAGGGGA[C/T]ATCACCACCAATCCC	9873
rs568878613	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72943427	GGTTTGAGTAGGAAA[A/G]GATTAGTGAGACACT	9873
rs568882636	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73035932	CACCATGTTGGCCAA[C/G]ATGGTCTCAATCTCT	9873
rs568905202	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990420	CTTCTCAGCACCACA[C/T]TGCACTTATTCCAAA	9873
rs568912121	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72998240	CTAATTCAAGGTAGA[C/T]TGTAGTAAGTTAATT	9873
rs568920425	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037195	AGTTCCCATGTATCA[C/T]TTGCCCCCACACATG	9873
rs568923835	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836297	ACACAATTCATTACT[C/G]CTTAGGGTGGAGGTT	9873
rs568929519	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936194	TTATTAAAATAATAG[G/T]GCTTAACCATTTCTA	9873
rs568939818	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982497	TGTTTGGGTTTTGGG[A/G]AAACAGGAAAGAATG	9873
rs568941095	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72994660	AGTCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA	9873
rs568951636	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061168	CATGGAAGGCGAGCC[A/G]AAGCAGGGTGGGGGG	9873
rs568954296	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983131	AACCCCGTCTCTACT[A/G]AAAATACAAAAAATT	9873
rs568974951	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72929191	TAAACATACGTGTGC[A/G]TGTGTCTTTATAGCA	9873
rs568976088	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908422	ATTGCTGAATCATAA[C/G]GCAGTTCTATTTTTA	9873
rs568998199	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73092310	TTTTTTAAGTTTTTG[G/T]TTTTTTTTTTGTAGA	9873
rs568999995	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083805	AATGTAAATCTATCA[A/G]CACACCTTCAAATAC	9873
rs569001228	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72929817	TATTGAAACCATTTA[C/T]ATACATGTCAGATTT	9873
rs569004335	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73032685	TAAAGCAGAGAGATC[A/G]AGTCAGGGAAGGCTT	9873
rs569004417	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72991609	GGCTGGTTCAACATA[C/T]GCAAATCAATAAACA	9873
rs569012854	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052932	GCTCACTGCAACCAC[C/T]GCCTCCTAGGTTCAG	9873
rs569033485	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72875971	GCCCAGCCCTCTGGC[C/T]AGTCCTCTAGCTGAA	9873
rs569036480	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73100659	TGAGCCACCGTGATC[A/G]GCCTACATACATTTT	9873
rs569041078	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970814	TTGGGGTTAGGTATA[C/T]AAAATGGGACAAAAC	9873
rs569043960	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73127856	CTTTGGGTTGGGGGG[C/T]GGGGGTGGGAATCAC	9873
rs569047846	snp	C/T	0.000166324	0.00911779	intron-variant	FCHSD2	GRCh38.p7	11:72867860	TCCAAGAAAAGAAAT[C/T]GTACCGAGTGTAAAG	9873
rs569058383	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72967844	TGCCTGTAATCTCAG[C/T]ACTTTGGGAGGCCGA	9873
rs569061803	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73084662	GCCTCCCAAAGCATT[G/T]GGATTACTGGCATGG	9873
rs569075316	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076418	ACCTCAAAAATATCT[A/G]CTAAGCGAAAGAAGA	9873
rs569083537	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72868372	CGATGGGTGGGGAAG[C/G]AGAGCATTAAAAAGA	9873
rs569088779	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075532	AATGATACAGTCAAT[C/T]TGGAAAACAGTTTGA	9873
rs569097479	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73135015	TGCGCCACCATGCAC[A/G]CCTAATTTTTGTATT	9873
rs569102737	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73008830	AGCTACTTAACATTT[C/T]AGATATGAAGAGATC	9873
rs569105420	snp	A/C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135830	ACTGTATCATAATTG[A/C/G]TCTCCTCCCCTCGAA	9873
rs569106780	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974811	AAAGAGGGCATTAAA[A/C]AAAAAAGGATATAAA	9873
rs569116388	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945487	TCAGGACATAGGCAT[A/G]GGCAAGGACTTCATG	9873
rs569138379	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067989	ACATGGTGACAGACA[C/T]GAGAGAATAAGAACC	9873
rs569150467	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067442	ATGTAACAAAACTGC[A/G]CGTTCTGCACATGTA	9873
rs569167163	snp	C/T	0.000153498	0.00875932	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73015821	TACCTGTAATCATTC[C/T]GATCATCAGCTTTTA	9873
rs569178338	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73015124	GCTGGGATTACAGGC[A/G]TAAGCCACTGCCCCT	9873
rs569183561	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72957232	TATTCCCCTTCCTGT[A/G]TCCATGTGATCTCAT	9873
rs569194244	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72966627	ATTCCTGCATGAATA[C/T]ATTCAACAGATATAT	9873
rs569195085	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959049	TGCGTGCATGGGACA[C/T]ACATCTCCTTACATA	9873
rs569197266	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72961757	TAATCACATGTCAAG[A/G]GAATCATCAATAGTC	9873
rs569208960	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143127	GGCGGCACTCTACTG[A/C]AGGGCATTCAAGTCA	9873
rs569228882	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72875393	TATTTGACAGAGTCT[C/T]GCTCTGCTGCCCAGG	9873
rs569232219	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967581	AATTCAGAGACAGAA[A/G]GCAGATTAGTGGTTG	9873
rs569236777	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086214	AGGAGTTTAAGACAG[G/T]CCTGGCCAACATGGC	9873
rs569237649	in-del	-/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72934388	AGGCTGGTGTGCAGC[-/G]GGCACTATCTCGGCT	9873
rs569239313	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952078	CTGCATATGTCTTAC[C/T]AAATGAAGACAAGAT	9873
rs569264935	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860388	GTTTATACTGGGTTA[C/G]AAAACAAAGCTCAAA	9873
rs569275023	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72852704	GCACGTGTATATTCA[C/T]TGCAGCACTATTTAT	9873
rs569276374	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72861148	CATATAATTAATAAA[C/T]CTCTAGCAGAATGAT	9873
rs569278371	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142218	GGGCGGCGGGTTAGC[C/T]GCAGCCGCGTTGTCC	9873
rs569288975	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73063198	TAACTAAGCTTCATA[A/C]GCAAAGGAGAAATAA	9873
rs569297352	in-del	-/AAA	0.00451692	0.0473081	intron-variant	FCHSD2	GRCh38.p7	11:73049873	GCACAAAAGGACCAT[-/AAA]AAAAAAATTGTTTTC	9873
rs569298600	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900307	AGAGCTCAATATCCA[C/T]CAGTTGGGCGGCTTT	9873
rs569311623	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72903465	ACCTCGTGATCCACC[A/G]GCCTCGGCCTCCTAA	9873
rs569328449	snp	C/T	0.0134861	0.0810011	intron-variant	FCHSD2	GRCh38.p7	11:72846085	AGATAGATAGATAGA[C/T]AGATAGATAAGTAGT	9873
rs569346616	snp	A/C	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72902834	TGTCCTATTTTCTCA[A/C]AAATAAATTTGGAAA	9873
rs569348568	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108411	GCTTTTTCACTTCAT[A/G]TAATCCTATTTGTTC	9873
rs569349502	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064050	TGAAAGTAAAACACT[C/T]CTCAGCAAATGCAAA	9873
rs569351360	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72912457	TTGAACCATCCCTGC[A/G]TTCTTGGGATACATT	9873
rs569352243	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73101592	ACAGATGCACATACC[A/G]TGCCCAGCTAATTTT	9873
rs569369595	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73100750	CGCAGCTTGGATGTG[G/T]TAATGTTGAAATTCG	9873
rs569386078	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045214	AAATTAAAACCACAA[C/T]GAGATACCATCTCAC	9873
rs569412648	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108881	CAGCCTAGATTTAAG[G/T]TTTTAACACAATTTG	9873
rs569413279	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056736	TACTACAGGAGAGCA[C/G]ATGAGAGCCATCAAA	9873
rs569413623	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72910282	TGGGAAGTGAGGAGC[A/G]CCTTTGTCCGGCCGC	9873
rs569432631	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73093465	GGTATTAGGGATTCT[C/T]GAACTTACAGCTGGT	9873
rs569433531	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73112214	TTTTGTTTGTCTGGA[A/G]AAGCCTTTATTTTTC	9873
rs569449605	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72891490	TTGGGGTTATCAGAA[A/G]TTTGGGAATGAACTT	9873
rs569451567	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72853770	TGCATCAAAGAACAA[C/T]AGAGTGAAAAGACAA	9873
rs569452200	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72964875	GCTCACTGCAAGTTC[C/T]GCCTCCCGGGTTCAC	9873
rs569456432	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72985264	AAAACCAAGAGTAAT[C/G]ATTATTTTCCTTTAT	9873
rs569463830	snp	C/G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72892681	ATGATCTCAGCTCAG[C/G/T]GCAACCTCCACCTCC	9873
rs569466177	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73000478	AAAATATGTCCATTT[A/G]AAAACATTTACTCAT	9873
rs569467213	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73029845	AGGCACAGGCTCAGA[A/G]AATTCCTGAGAAGAC	9873
rs569467634	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73038168	AGGCAACAAGGAGAT[C/G]TGTCTCTATTAAAAA	9873
rs569485095	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72948077	CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC	9873
rs569499559	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72885189	CCCTCATATTTGCTG[A/G]CTAATTTTACTTAGG	9873
rs569512149	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72888132	AACAAGATAGCCAAG[C/T]ATAGGAATCTGAGAA	9873
rs569514783	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73096709	TTCACCACTGAGTAC[A/G]ATGTTACTGTGAGCT	9873
rs569522789	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72948727	CTGGAGTGCAGTGGC[A/C]CAATCTCGGCTCACT	9873
rs569528182	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72992979	AACAGGCAACCTACA[C/G]AATGGGAGAACATTT	9873
rs569533678	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72921729	TTTGTTCGTTAATGC[A/T]TTCTTCTAATATCAC	9873
rs569538658	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72943136	AGCTAGGATTACAGG[C/T]GCGTGCCACCATGCC	9873
rs569570999	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909876	AGTGCCTCTGCCCGG[C/T]AGCCGCCCCATCTGG	9873
rs569607790	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903762	GCAGAAGAAAAAAAA[A/G]GTTCAAAGTAACTCT	9873
rs569609253	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72941743	CATACACTGCTTTCA[C/G]AAGTATATACTGATA	9873
rs569610791	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071763	GGAAATGGACAGAGT[A/G]AAACACAGGTTTCTT	9873
rs569618032	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848615	CCCCCAGTGTATCAC[A/G]TATTGGGCACTCTAT	9873
rs569620162	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73118224	CTTGGGAGGCTGAGG[A/C]AGGAAAATTGCTTGG	9873
rs569627918	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73111326	ATATTTACAACTGTT[A/G]TATCTTCTTGCTAAA	9873
rs569630454	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970753	AAAAGACTTCCATGA[A/G]GAAAGGCCGCTGAAC	9873
rs569639019	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019047	AAACAAGTGGCAAAA[G/T]GTGATATAAGTACCC	9873
rs569670246	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73138900	GGTGTCAGTGACTGC[A/G]CACGGCCTCGCATAG	9873
rs569674491	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72864607	TTGTTTGTCAATTAA[A/G]AAATAAATAAATAAG	9873
rs569675250	in-del	-/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72885214	TTAGGCTATTTTTTG[-/T]TATCTGTTAAGTGGA	9873
rs569681964	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72963408	TGAGCTAAGTGAGGC[A/C]TACAGAAGGGAAATA	9873
rs569690360	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72910254	AGGAGAGCCTCTGCC[C/T]GGCCACCCCATCTGG	9873
rs569707734	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73090751	ATGTGCATATATATA[A/G]TGCATGTTTTTATTG	9873
rs569735489	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011381	GGAACATGTGCACCA[C/T]CTAGGCTAGCAGGTG	9873
rs569749918	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73017044	CTGGAGTGCAGTGGC[A/G]CGATCATGGCTCAAT	9873
rs569770576	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73082623	ATGCCCCAATCTCTC[A/G]TTATTTATAATGAGA	9873
rs569786279	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73038400	ATTGATTCTTAAAGG[G/T]ACCTTATAATTTATC	9873
rs569787141	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041468	GTTTTGATTTTCATT[C/T]CCCTGATGATTAGTG	9873
rs569805158	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842282	CTAAGAGTTTTACTA[C/T]GTAAATTAACCACAG	9873
rs569812244	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72849396	AAGATTAAGTTTGGC[G/T]GAGCAGAAGTGCTAT	9873
rs569827877	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73057064	CTCTAGCCTGGGCGA[A/C]AGAGCAAGACTCCGA	9873
rs569842094	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72865866	AAGTGTGCTACACAG[C/T]AGTCCAGTCATACAC	9873
rs569847493	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72933588	GATACCCAACTTATA[C/T]TAGCCATATCCAAAT	9873
rs569852212	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896629	AAAAGTCCCAAGGGA[C/G]TTTTAGTGATCAATC	9873
rs569854738	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137552	CATTCGACAACAAGG[A/G]TATAAAGATACAAAA	9873
rs569858287	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73003384	GTAACAGCAGCAGAA[C/T]TGTAACAAATAGAAG	9873
rs569861872	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880940	ACTAGTACAAGAAAA[C/G]ATAGGGGAAATGCTT	9873
rs569864300	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72846900	TAGAAAAACTCTTGA[C/T]GAAAATTTCAGTAAG	9873
rs569868031	in-del	-/AT	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72973418	GGTAAGTTATTTATG[-/AT]ATATATATATACAAT	9873
rs569885893	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72996486	AAAAGCCTTAAGTTA[C/T]TGTAGCTCTCATTCT	9873
rs569892558	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73090435	TTTCACCGTTTTAGC[C/T]GGGATGGTCTCGATC	9873
rs569894186	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850643	CAGGTGTGAGCCACC[A/G]TGCCTGGCCAGGACA	9873
rs569902323	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73122846	ATAGTGTGGCTGTTC[C/T]ACTACATTTACAAAG	9873
rs569906138	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72866626	ACCCCAAAGTCAAGT[A/G]GGTGATGTTTCTTTT	9873
rs569911157	snp	C/G/T			intron-variant	FCHSD2	GRCh38.p7	11:73093431	CCTCCAACCTTGAAG[C/G/T]TGGTGTCAAAGTGAA	9873
rs569916280	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73136898	TTAGCCGGGCGTGGT[G/T]GCAGGTGTGGTGGCA	9873
rs569920150	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72858409	AAAGAAAATGTGGTA[C/T]ATATACACCATGGAA	9873
rs569931955	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042100	CCCAGCTAATTTTTT[A/T]ATTTTTAGTAGAGAC	9873
rs569939928	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72888594	TTAGAGTTTAGTCTT[C/T]GAGATATATTTTCTT	9873
rs569954067	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115741	GAGATAGGAGTTGAT[G/T]CTGCAGTCTTGAGGC	9873
rs569965203	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934205	CACGTATGATGAAGA[C/T]GCATCTGTATCTTGT	9873
rs569982563	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144269	GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCCGAG	9873
rs569982656	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004910	TTTCAGCCAACAGTG[A/G]CACTATCAGAAGGCA	9873
rs570007396	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072815	GAAATTCACCAAAAA[A/G]GAACCCCCACCACAT	9873
rs570015619	snp	G/T	0.00199481	0.0315187	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839367	GTTTTTGGTGGATTT[G/T]AAGCAATATCAGATC	9873
rs570020991	in-del	-/GT			intron-variant	FCHSD2	GRCh38.p7	11:73051815	TTCAAATAAGTATTA[-/GT]GTTTTCAGGCTTTTT	9873
rs570027904	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035044	GATTCTGATATGCAG[C/T]CACTATTGGGAACAA	9873
rs570031248	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73083860	AAGGACAATATTTTA[G/T]TCATCTTTATGTGCT	9873
rs570031472	snp	C/G			missense, synonymous-codon, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842629	CAGGTACCTGAATCT[C/G]TCTCATCCATGGAGT	9873
rs570041727	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72977028	CTTCCCGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	9873
rs570044903	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005857	GTTTTAAAGCCATCC[A/G]GTCTCATGGCTTTAA	9873
rs570044940	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997523	AAAAACCGCAGGCGG[A/T]TAAAAGAGACCTACA	9873
rs570046413	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927424	GTGTAGGTTCATCAA[C/T]TGCAACAAATGTGCC	9873
rs570066566	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72874182	CTTGCCCTAGCACCA[C/T]TGTAGTATGCTTTTG	9873
rs570070647	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73087726	AAAAAAAAAATTTTT[A/T]AAATAAATTTAGTGC	9873
rs570073197	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875156	GGACAAGGACTGTGT[A/G]TAATGTATTACTATT	9873
rs570085312	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73116966	CAAAAAAAATCACTA[C/T]TGTTATATCTCTGTT	9873
rs570093633	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72850828	TGTGTGGTGGCTCAC[A/G]CCTGTAATCCAAGCA	9873
rs570105252	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093779	GCTAATTTTTTTTGT[A/G]TTTTTAGTAGAGACA	9873
rs570112067	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73130040	CACCCGCCACCACGC[C/G]CAGCTAATTTTTTTT	9873
rs570114906	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72947911	ATTTTAATCAGTTAA[C/T]ACAGTGTTAACATTT	9873
rs570142990	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028457	AAATGCCTGTACCCC[C/T]ATTGTATCTTGGAAG	9873
rs570150839	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976168	AAATCTGCCTAATAA[C/T]ATACAGACAGAGAAA	9873
rs570172851	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021034	GGTGCATGCCACTGC[A/G]ACCAGCTAAGTTTTA	9873
rs570188515	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72873101	TCGGGAGGCTGAGGC[A/G]GGCAGATCACCAGGT	9873
rs570193344	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72965096	GCCTGGCCAATCATT[C/T]TACTTCTTAATTCAA	9873
rs570205072	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911525	ATCTCTGTGAAGAAT[A/G]GCACTGGTATTTTGA	9873
rs570220088	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014238	CTGGGCTCAAGCGAT[C/T]GTCCTGCCTTAGCCT	9873
rs570237505	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72976798	CTAAGAACATACACT[A/G]GGGGAAAAGTGCTGG	9873
rs570243606	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72869573	CTTCACGAATTTGTG[C/T]GTCATCCTTGCATAG	9873
rs570274903	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956845	AAAAAAAAACCAACC[C/T]TAGAAGACACCAAAT	9873
rs570283915	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72912174	AGCTAGGACTTCCAG[C/T]ACTATGTTGAACAAC	9873
rs570285547	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72995671	TTCATGCCACTGCAC[G/T]CTAGCAGGGGTGACA	9873
rs570289293	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905888	ATTGTGAATAGTGCC[A/G]CAATAAACATATGTG	9873
rs570293033	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73012703	GGGAGTCATTGTATA[A/C]TTCTTCATCTCTCTC	9873
rs570301976	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058424	GCCCATCAATTATCT[A/G]AACAACAAACTGACT	9873
rs570305770	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72870129	TTGATGCCTGGTGAG[G/T]GCTTATCTTTTGACG	9873
rs570317878	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862246	CTCTCACCACTTCTA[C/T]TCAGCAATTTTATAG	9873
rs570318515	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72937616	CCAAAGTGCTGGGAA[C/T]ATAGGCGTGAGCCAC	9873
rs570330823	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72887128	ATTGATATATAAGGA[A/G]ATATATATATATATC	9873
rs570354361	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73021753	CAGAATTCTAAAAAA[A/T]CTAGATGCAGAAGAA	9873
rs570361654	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72892804	AGAGACGGGGTTTCA[A/C]CATGTTGGCCAGGAT	9873
rs570375055	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898391	TGTAAGGCAAGGGCA[C/T]ATGCAAAGTATATGT	9873
rs570382455	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73064822	AAAGAAGTCGAATCC[C/T]TGAATAAACCAATAA	9873
rs570404938	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73086167	AATCCCAGCACTTTT[A/G]AGAGATAGAGGTGGG	9873
rs570416248	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73038110	AAAAATTCTTATGAC[A/G]AGGTGGGAAGATTGC	9873
rs570434062	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72958904	CCATTTCCATCTATG[A/G]AAACAGAAGCACTGG	9873
rs570441726	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73000654	CAAGAACTAGTGGGA[C/T]TAATAACCTTGTAAC	9873
rs570475349	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73031042	CTTAAAAAAAAGGGA[C/G]ATCCTGCTATTTGTC	9873
rs570480630	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076701	TATGTAAATTAAAAG[C/T]ATACATAAAAGTATT	9873
rs570502752	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73001347	GGGAGTTCTGATTCA[C/T]TAGTTATTCTTAATA	9873
rs570503484	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023743	AGCTTTATTGATAAA[C/G]TTGGCAACAAAGATG	9873
rs570510605	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115641	CAGACAGACATAAAG[A/G]TATTTATTTTAAGAA	9873
rs570514493	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72968224	TACAATGTAGATGCT[C/T]CAAAATTACTTTCTG	9873
rs570518971	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72930870	GAATAAGACCTACTA[C/T]TTGATAGCACAATAG	9873
rs570527802	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73034995	ACTCTAGAGGTGGGG[C/T]TGAGACACTGATAGT	9873
rs570538667	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031677	AACCAACACTGCTTA[C/T]ACCCAGGAATCCAAC	9873
rs570558210	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914275	CCACCGTGGCCTCCC[A/G]AAGTGCTGGGATTAC	9873
rs570560561	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016730	AAGACAGATTTTAAG[A/G]GTCTTTTCTTTTTAA	9873
rs570586868	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73089066	AATTTCCTGTTTTAA[A/G]GCAAAAGACAAATCT	9873
rs570589661	in-del	-/AT	0.00438332	0.0466095	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836470	CCTCCCTTCTAGCAC[-/AT]GTCCCACAGTACTGT	9873
rs570595382	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72923132	ATTCCTTTTTACAGC[G/T]TAATAATATTCAGTT	9873
rs570600806	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039887	ATCATTTTGAAGTTT[A/C]TTTTTAAATTTTCAT	9873
rs570602438	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960593	GTTCCATGCAGCTGC[C/T]ATTAATTTCTTACAA	9873
rs570619426	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886466	TTTCTGTGGCCTCTG[G/T]GTTCTTCAACTATAC	9873
rs570637642	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73069172	AAAAATTAGCCAGGC[A/G]TGGTGGCATGCACCT	9873
rs570646905	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115079	CTGCAGTGGCAAGGC[A/G]TGCTGAAATTCAAGT	9873
rs570661186	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73033011	GTACTTAGATTGGCC[A/G]GGTGCGGTGGCTCAC	9873
rs570663796	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73032808	ATACAAGCTGGCATG[C/G]AGCTTGTAAAAGGGA	9873
rs570665815	snp	A/C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72974953	TACAAGAGCTAGAGA[A/C/T]GACAGAGAAACCAGA	9873
rs570680269	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72914889	ATTGACAAATGGGAT[C/T]TAATAAAACTTAAGA	9873
rs570698651	snp	A/G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73061705	GCCTCTGGGAAGTTC[A/G/T]AACTGGGTGGAGCCC	9873
rs570700674	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901920	CACTCTGTCATCCAG[A/G]CTGGAGTGCAGTGGT	9873
rs570717496	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72924220	AGCTGGGACCACAGG[A/C]ACTCACCACTGCATC	9873
rs570724350	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054028	GTCCTCACAACAGAT[A/G]GTTTGAGTGCACAGG	9873
rs570725742	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73033266	GCACTCCAGCCTGGG[C/T]AACAGAGCGAGATTC	9873
rs570731317	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054892	GAGGACTGCTTGAGA[C/T]CAAGAGGTTGAAGCT	9873
rs570735377	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846810	GAAAATATGCATAAT[G/T]GAGCTCTTACGGTAC	9873
rs570739886	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72961308	AGCTCACTATAGCCT[C/T]GAACTCCTGGGCTCA	9873
rs570743155	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72953015	ACTTTGACTTGAAAA[A/G]ATTTTGTTACTGAAA	9873
rs570743168	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73121751	TATAATTTATAACAG[C/T]GGTCCACAAACTTTA	9873
rs570771448	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062232	GCCTGTCAGAAGGAA[A/T]ACTAACAAACAGAAA	9873
rs570773406	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72909301	CTCGGCCTCCTGAGG[C/T]GCTGGGATTGCAGAT	9873
rs570777213	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024843	AAGGACATGAACAGA[C/T]GCTTTTCAAAAACAG	9873
rs570782310	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73046101	ACTCAAGGGATACTG[C/T]GGCCTCAGCCTCTGA	9873
rs570788898	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72912739	TAAAATTCAGCAGCA[A/C]AGCCACCCAGTCCCA	9873
rs570790346	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73091604	GACAGAATTATAGAA[C/T]GTCAAACCACATTCA	9873
rs570792588	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73021982	GTGTATGGCAGGAGA[A/G]GGAGAGGAGAATGAG	9873
rs570806242	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120721	GCAACAACAGCAAAA[C/T]TGTGTCTAAAAAAAT	9873
rs570812123	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902822	TTATTATTTATCTGT[C/T]CTATTTTCTCAAAAA	9873
rs570827628	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934823	CAAACTTTTTGACTA[C/T]TGGACACAAATTTCT	9873
rs570830672	snp	G/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72945653	GCAATCTACTCATCT[G/T]ACAAAGGGCTAATAT	9873
rs570837587	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939485	GAGTTATAGAGATTT[A/C]TTCAGATGTTAAAAG	9873
rs570855982	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73052111	GAAACTTAATAAATG[C/T]AAAGATAGTATGGCA	9873
rs570864224	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73081175	GCACTGTGGCTCATG[C/T]CTGAAATCCCAACAC	9873
rs570866353	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72986386	AGCTAATTTTTTGTA[G/T]TTTTAGTAGAGACGG	9873
rs570866991	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129463	AGCAGCATTAGATTC[C/T]CATGGCACGAACCCT	9873
rs570869962	in-del	-/TTTG	0.00120651	0.0245316	intron-variant	FCHSD2	GRCh38.p7	11:72901872	TATTCTGGTTTTTTT[-/TTTG]TTTGTTTGTTTGTTT	9873
rs570870808	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72847709	TTTTTTTTTTTTTTT[C/T]TGAGACAGAGTCTCG	9873
rs570890950	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73103411	CTGCTTCCATTTTTA[C/T]AAGATTTAATTAGAC	9873
rs570894222	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897422	GGACCATTATTAGCA[C/T]AGCATTTACATTGTA	9873
rs570894555	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135894	GCGTTGCAGCAGTAG[C/T]GGCTCATTTCTGTAA	9873
rs570898083	snp	C/G/T	0.00119737	0.0244387	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839132	TCCTATGACTAAGAT[C/G/T]CTAGCACATCCTCCA	9873
rs570900044	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946070	CAAAGGATTATAAAT[C/T]ATGCTGCTATAAAGA	9873
rs570900072	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73025666	TAAAAATTAAATAAA[C/T]AGAATTTTAAAAATT	9873
rs570910303	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72846417	GAACTCCTGACCTCG[C/T]GATTCGCCCGCCTTG	9873
rs570913494	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73046984	TGATGCTGTCAATAA[A/T]ATGAGGTCTTTCTGT	9873
rs570925420	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72932155	ACATACTGTTAATTA[C/G]CAAATCTTATTGATT	9873
rs570926266	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73094976	TCTAACATCCATTGA[A/C]TATCTTCTGGATTTC	9873
rs570933947	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73138713	TACTAGGTTCAAGCA[A/G]TTCTCTGCCTCAGCC	9873
rs570937079	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72980341	TCATGAATCTGCTCC[A/G]TCGAAACTTTTCTTC	9873
rs570938375	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994582	ATAGTGTAAACTCAC[A/G]GTGAAACCCCGTCTC	9873
rs570951848	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143253	TTTCTAAAGGTTACA[C/T]AGCAGGACTAGAATC	9873
rs570990869	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72871164	CGATCAGAAAGTAAC[C/T]GCTGCTTTGCTCCAA	9873
rs570993357	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72940127	AATTCCATAGAAGCA[A/G]GACAAATAAAATTTA	9873
rs570998273	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73017067	GGCTCAATGCAGCCT[C/T]AACTTCCTGGGCTCA	9873
rs570998702	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042746	TTCATCAGTGTTTTG[C/T]GGTTTTTTGTTGTAG	9873
rs570998727	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72976230	GGCATAAGAAATAAA[C/T]AGTATTTCTTGGGGA	9873
rs571009000	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73079864	CCAAGCAGAGACACA[C/T]TGGAGTATTTTAATT	9873
rs571024610	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72955223	CTATGACACCTTTCT[C/T]AGGGTCGATTAGTTT	9873
rs571033774	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73026370	ATTACAGTTGCTCTT[A/G]CCACTGGGAGCAAAA	9873
rs571049281	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087857	ACTTCCAGTCTCCTA[A/G]GCTCCATTCATGGCA	9873
rs571055176	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978103	ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA	9873
rs571059348	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879891	GTAATCCCAGCTACT[C/T]GAGAGACTGAGGCCG	9873
rs571060441	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73035429	CACCTTTGGCCTCCC[A/G]AAGTGCTGGGATTAC	9873
rs571071138	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73071327	CATTTTCCCAAAAAG[C/T]ATGATTTCCAACCCC	9873
rs571072019	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73086453	TCAATCTCAAATCAA[A/C]AGCCTAACTTTACAA	9873
rs571082990	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990670	ACCAATGAGAACAAA[C/G]ACACAACATACCAGA	9873
rs571084851	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952160	TTAACTTATATTGGT[C/G]TTGCTTGGTCACTCA	9873
rs571091069	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72978966	GGTTCAAGCGATTCT[C/T]GTGCCTCAGCCTCCC	9873
rs571098883	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018458	CATCATACACTGTTA[C/G]TGTCTGGTTTAAATA	9873
rs571117273	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927716	GCACAGTTACTTTAG[C/T]TGACTAGGTTGAGCA	9873
rs571124047	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72941963	TTAATGGCATATTAA[C/T]ATGATCAAATACTAT	9873
rs571137650	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080750	GCAGTTCAAAACCAG[C/T]CTGGACAACATTGTG	9873
rs571144644	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72996752	ATCAGACTACCTTTC[C/T]CTAGACTGGAAAGTG	9873
rs571150248	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72986684	TGCATGTAGATCTTC[C/T]AATATAAGGTTTTAA	9873
rs571161180	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027163	AAGAGAGGAGGATGT[A/C]GGAAAGTTTGGAACT	9873
rs571187501	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970070	AGAATACCAGTAAAA[A/T]GAACCCAACTTGCTG	9873
rs571192189	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73048903	AACGACCACACAAAC[A/G]TAGCAAGATGTTGAT	9873
rs571195619	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837888	GCGTCCCCAGTAGAG[A/C]AGCTCAACAATGCAG	9873
rs571196435	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73118137	CAGCCTGGCCAACAT[-/G]GTAACACCCCATCTC	9873
rs571204644	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928368	TCTCATTAGCACCAT[A/C]TCTCATCACTGTTCT	9873
rs571211406	snp	A/C	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73004767	TTTAAATTGATGTCA[A/C]ATAAATGCTAGTAAC	9873
rs571218605	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956781	TGGGGAAACTTCAGA[C/T]CATAGCACTATTGCA	9873
rs571222857	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73106501	AAAGAACCCTGAAGT[A/G]CAAACTGTTACAGGA	9873
rs571228015	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73106051	ACTGGGATGAACTTT[A/G]GAAATTATGTGGAGA	9873
rs571230289	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73077791	GACACACAGGAAAAC[C/T]CTGGGGGCTTACAGA	9873
rs571242828	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72919822	ATTAGAATAAATGTC[A/G]TTGGATTAAAAATAC	9873
rs571267844	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997991	AACTACCACTCCCGT[C/G]CCCAAAAGATGAGTT	9873
rs571276243	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125270	CTTTTTAAAAGATAC[C/T]TGTTTAAAGAAAACT	9873
rs571298552	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72952329	CCAAGTTTGACTATC[-/T]TTTTTTTTTTTTTGA	9873
rs571299177	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942629	TGTACTTTTCAAATT[C/T]TCTTCTGGTACTTTG	9873
rs571321824	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943290	GACCTACTTTGCCCA[A/G]CCCTGACTTTTATAT	9873
rs571328364	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889544	GCAAGACCCTATCTC[C/T]ACAAAAAATCTAAAA	9873
rs571329020	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73117159	ACTTATAACAAATAC[A/G]TTCTACATGTACTAA	9873
rs571329958	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990340	GCATCAATTTGGGAT[A/T]AACTAAAAATTAACT	9873
rs571333497	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73098491	CTGGAAAATGTTTTA[C/T]GTGTACTTGAGAAAA	9873
rs571344661	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73082893	ACAACCATAAAATGA[C/T]ACATCAACATAATTT	9873
rs571355456	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067269	TCTCACTCATAAGTG[A/G]GAGTTGAACAATGAG	9873
rs571366013	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028703	CAATTCTCAACTGGA[A/G]TTGTAATCCCCATGT	9873
rs571368758	in-del	-/G	0.00558655	0.0525553	intron-variant	FCHSD2	GRCh38.p7	11:73089972	TAATTAAAATAGCTT[-/G]GTAATGGAACATAAG	9873
rs571383553	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72883033	TAGTTGTTTTCAATA[C/T]GGGTGCAAAGGTAAT	9873
rs571390495	snp	A/G	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73124436	TAAAAAAAGAAGAGA[A/G]AGAATGGGGCAGAAA	9873
rs571417047	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140202	TTCAGGAAAATACAT[C/G]TGTCAGAATATGTCT	9873
rs571420558	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73060215	CTCAGGAAAGTAACA[A/C]CCATTCAAGGAAGTT	9873
rs571461946	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72909800	GCACCTCTGCCCGGC[C/T]GCCCCGTCTGAGAAG	9873
rs571462996	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091711	CCACTTGGAATTTCC[C/T]CCCGTTATTTGGCCT	9873
rs571465192	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72981615	GTGCTAAAAATCATC[C/T]TTAGTAAATGTGTTC	9873
rs571472672	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084583	CTTCTTGTAGAGATG[G/T]AGTCTTGATATGTTT	9873
rs571479975	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73061071	TCCCAGCAAGATCCT[C/T]GCAGAAGGCAGATGA	9873
rs571493242	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73029712	ACTTAAAGGGACAGC[A/G]TCCTTTTTCCCTGTC	9873
rs571498872	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029233	GGAAAACAAAAGATA[C/T]GGAAACCACTTACAA	9873
rs571516408	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123255	ATGTTGACTATCCAA[C/T]TGATAATTTTATACA	9873
rs571519430	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72973647	GGGAGATTTCCACTG[C/T]ACTGAGAGTGTTTCA	9873
rs571530842	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982246	TTTGCCTGAAGGTCC[C/T]GAGAACTGTCCCATC	9873
rs571536265	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075448	GGTATTTGCTAGGAC[A/T]TTACTAGAACTAGAA	9873
rs571539839	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73074854	GAGTTCGAGGCTGTA[A/G]TGAACTAGGATCACG	9873
rs571550090	in-del	-/TA	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73048778	AGACAGGGATGTATG[-/TA]TATAGTTCACCTCAA	9873
rs571550384	in-del	-/TTTT			intron-variant	FCHSD2	GRCh38.p7	11:72850077	TTTTTTTTTTTTTTT[-/TTTT]GAGATGGAATTTCGC	9873
rs571553947	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72845140	AAAAGCTATGGAGAG[A/G]CTGAGTGAGGTGGCT	9873
rs571556488	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73022978	GTGATGCTAGAACAA[C/T]TGAATGACCATAAAC	9873
rs571561446	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73022190	GAGTGAATGCTTTTC[C/T]CTTAAGATAGAGATA	9873
rs571576486	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73092683	TCAGTAGGTTAGCTC[A/C]TGAGACACACAGAAC	9873
rs571576591	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100321	AGGCACTGACCTAAG[C/T]GCTTTACATGCTTTT	9873
rs571579266	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966465	ACACCCGGACTAAAC[C/T]GAGCATATTACTTTG	9873
rs571590529	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944853	TACAAGGGATGTGAA[A/G]GACCTCTTCAAGGAG	9873
rs571599669	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059520	GGAATGCTCCCTACC[C/T]TTCACTCTAACTTCT	9873
rs571608740	in-del	-/GTAC	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73035181	TATGTATGTATGTAT[-/GTAC]GTATGTATGTATGTA	9873
rs571619432	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860352	TTTTTAAGAACACAT[A/G]TAACAGTTACCAAGA	9873
rs571621850	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72865513	TGATTTCTCTGGACA[C/G]GTCTCAAAAATACTC	9873
rs571622135	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72859410	GCTTGTGTTCAAGTA[A/G]CCCTTATTTTACTTA	9873
rs571628838	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72872157	TTTTTGGCTTAGAGG[C/T]ACTCCAATTGGTAAA	9873
rs571630857	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838278	CTTTCTCAGTCTGGG[A/G]ACTAACCTTGGGGAG	9873
rs571636690	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093343	TGAGAGTCCTGGCAA[A/G]TTATTGAATCTAAGG	9873
rs571638384	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913130	CAAGAGAACAGCAAG[A/G]GGGAACTCCATCCCC	9873
rs571642260	in-del	-/AAAC	0.0532157	0.154195	intron-variant	FCHSD2	GRCh38.p7	11:72855279	AAAACTCCGTCTCAA[-/AAAC]AAACAAACAAACAAA	9873
rs571650252	snp	A/C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72934048	TGGGAGGTTGAGGCT[A/C/G]CAGTGAGCCATGATC	9873
rs571657898	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72974684	TACTTTCAGTATTCA[A/C]AAGTACCAGTGGTAA	9873
rs571661940	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72867786	TTTAAAAAATTTTGG[C/T]TATTATTAAGTTTGA	9873
rs571666453	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959008	ATGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG	9873
rs571669745	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73014511	AAGACACCTTCCATG[A/G]TATCAGTAGGCCACT	9873
rs571676003	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72868308	AACAATGAGAACATA[C/T]GGACACATGAGTGGG	9873
rs571696188	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960784	ATAATAAAGAACCCC[A/G]GGGTGTGAAATACAC	9873
rs571698907	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907594	CTATTGAGATAATCA[C/T]GTGGGTTTTTTTTTT	9873
rs571699933	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952567	TGACCTCAAGTGATC[C/T]ACCGGCCTCGGCCTC	9873
rs571714234	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73081928	GCATTCAAGATCGGG[C/T]GCGGTGACTCACGCC	9873
rs571716936	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846371	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	9873
rs571751649	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73082559	CTACAAAATTAACTA[C/T]AATGAAATCAGAATT	9873
rs571753112	snp	A/C	0.00438332	0.0466095	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143121	GGAAACGGCGGCACT[A/C]TACTGCAGGGCATTC	9873
rs571760828	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73045881	ATGTAACTAACCTGC[A/C]CAATGTGCACATGTA	9873
rs571766372	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73048348	TAGTCTAGTACTGGC[G/T]TGTTATTTACAGGTA	9873
rs571778302	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72847082	GCTCACTGCAGCCTC[C/G]ATCTCCTGGGCTCCA	9873
rs571783502	snp	A/C	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73052811	ATAGCATGAAAAGAT[A/C]AGTTTCTACAGATAT	9873
rs571786801	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73052240	AATCTATGAAAAATT[A/G]TAAGTCAATAAACAT	9873
rs571788739	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73102129	GTAACAGTGAAAAGA[A/T]GCTTAACATCACTAC	9873
rs571790162	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72852238	CAGATGCTGGTGACG[C/T]TATGGAAAAAAGGGA	9873
rs571795945	snp	A/G			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140843	GGGGCCCCAGGGTTC[A/G]AAGTTAACGGTCAGT	9873
rs571799573	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999463	TAGCTGGAACTACAG[A/G]TGCACGCCACCACAC	9873
rs571818291	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73102523	GAATGAATAAACAAA[C/T]TGCAGTTGTACTCTG	9873
rs571822356	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138814	GGTTTTATCATGTTG[C/G]CCAGGCTGGTCTCGA	9873
rs571824222	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73079062	GATAATAGTTTACAT[A/G]AGTGTGTTCACAAAA	9873
rs571833639	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72993863	GTATACATATGTAAC[A/T]AACCTGCACGTTGTG	9873
rs571850676	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73094531	CAATGGGATCATGGA[C/T]AAACAGTAACATATT	9873
rs571851017	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73102792	TTTGGACTTCCCAGC[C/G]TCCAGAACTATAAGC	9873
rs571851553	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72900253	TGACCCACACCCCAT[A/C]TACCTCAGCTATGGT	9873
rs571853877	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944040	GGGAATCCTCCCTAA[C/T]TCATTTTATGAGGCC	9873
rs571860733	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991874	GATGCCCTCTCTCAC[C/T]ACTCCTATTCAACAT	9873
rs571862127	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991267	GATGGATTCACAGCC[A/G]AATTCTACCAGAGGT	9873
rs571892018	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72847898	GGGTTTCACCATGTT[C/G]GTTGGGCCAGTCTTG	9873
rs571896257	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986055	AAGCCAGTGTGAAGA[A/G]GATAGGAAAAGCAGC	9873
rs571896294	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839459	AAGAAGGCAACTTAG[A/G]AGACTTTTGTAATCC	9873
rs571914629	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73095552	AATAAAACTAGGAAA[C/T]ATATGTATGGACATA	9873
rs571928916	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73052995	GGGATTACAGATGCC[C/T]GCCACCACACCTAGC	9873
rs571938865	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72891485	CATTTTTGGGGTTAT[C/G]AGAAGTTTGGGAATG	9873
rs571959634	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840262	AGAAGGCACTCAATA[C/T]ATATTTGCTGAATGA	9873
rs571964629	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73109332	ATGGACATTTTAACA[A/G]TATTGATTCTCCCAA	9873
rs571979419	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72892558	TATCAAAGATCAATA[C/T]AAATCAGGATCTAGT	9873
rs571984091	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986499	CAGGCGTGAGCCACC[A/G]TGCCCGGCCCCAATT	9873
rs571989353	snp	C/T			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140409	CATTTCATGCACAAG[C/T]TCAATCCACGTCTAG	9873
rs571990935	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72874635	ACTACATTCTATTTT[C/T]TCAAAGCAGTTATTC	9873
rs571995302	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73054427	GTATTTCCTGTGATA[A/G]GGAATGATGGGCATG	9873
rs572016828	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879328	ACTCAATAGTCTTTA[C/T]AAGAAGAAAATAGAA	9873
rs572022112	in-del	-/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72887304	TTTGTTATATGTACT[-/G]CCTTCCACAGAGCAG	9873
rs572025673	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73118275	GGTGAGCCGAGACTG[C/T]GCCACTGCACTCCAG	9873
rs572051889	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73084882	GAGTTTAAAGACTTT[A/G]CCGTTATGTGCCAGG	9873
rs572055260	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837061	TAAAGACAGAATACA[A/G]GACTGGGTGGCAAGA	9873
rs572064960	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945778	GACATTTATGCAGCC[A/G]AACGATACATGAAAA	9873
rs572090745	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72901442	AAGTAAAAATAAAAA[A/C]AAAAATTGCCAGTTG	9873
rs572094376	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909165	CCTTGGCCTGCTGAG[G/T]GTCTGGGATTGCAGG	9873
rs572099225	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72939006	TGAGCTACTAAACAT[A/G]TAATGCAGGATATTT	9873
rs572105193	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72981988	CCCTGTCTCAAAAAC[C/T]ATATATACTAAAACA	9873
rs572126291	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73017702	GTACGGTAGTTTTTC[A/C]CCTCTGCACCTTGTT	9873
rs572131133	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902222	TGGAGGGGTACAACA[C/T]AAAAAATTTCAGGGA	9873
rs572131776	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886151	CAGGGATTCCTTGTA[C/T]TGGGTCCCTGAAAGA	9873
rs572138563	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72872380	TACATGCAACCATCA[C/T]CACAGTCAAATTTAG	9873
rs572142986	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73131731	AAATTAAAAAATTTA[A/C]AAAATAAGAACACCA	9873
rs572143108	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123417	AGCGCTCATCCTTAA[A/T]TACAAATGAGAATCA	9873
rs572153041	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73021031	GCAGGTGCATGCCAC[C/T]GCGACCAGCTAAGTT	9873
rs572153390	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72951669	TTACATTTATCTTTA[A/T]CAAACCTATAACTTA	9873
rs572164226	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73022534	AATCCCACAAAATGT[C/T]TGCAGGATCTGTATG	9873
rs572183490	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018729	AATTTTCATGTACTC[A/T]AATTTTTTAATAACT	9873
rs572193296	snp	C/T	0.0189856	0.0955633	intron-variant	FCHSD2	GRCh38.p7	11:72917682	CTTGACGTCAGGAGT[C/T]CAAGACTAGCCTGGC	9873
rs572211986	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73002885	TAATGTAATTGTTTA[C/T]TAACATCTGTCCCTC	9873
rs572275441	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886817	TCCCAACCTCTCCCT[A/G]TCTAGAGCAGGGAGT	9873
rs572280189	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72939743	TATGCCTCAGCCTCC[C/T]GAGCAGCTGGGATTA	9873
rs572301410	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025681	TAGAATTTTAAAAAT[G/T]TTTTAAATCTCCTTG	9873
rs572311350	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931563	CAAGGTCAGGAGTTC[A/C]AGACCAGCCTGGCCA	9873
rs572338854	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088235	AGATATGTTTTGATA[C/T]ATAAATACCATCATG	9873
rs572342014	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880014	CAAAAAAAAAAAAAA[A/G]AAAAAAAGTAATCCT	9873
rs572347904	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72969493	CTTAATTTTTTGAGG[G/T]TAGAGAGTATTTGTC	9873
rs572348665	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932377	TCTACACTGTTCACT[A/G]GCTACTCATCACATT	9873
rs572356421	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915964	AGCAAACTAATGTAG[A/G]AACAGAAAAGCAAAT	9873
rs572370600	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73043827	GCTAGATGTAGAGGA[C/T]CCATTGAGGACTTGA	9873
rs572376555	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129578	AACCCCAGATGGGAC[C/T]GTCCAGTTGCAGAAA	9873
rs572400334	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72973054	TAAAACAATAAACAA[C/T]TAAAATTTCCATTAA	9873
rs572401778	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73080195	CCAGCCACTCAGTAG[C/G]CTGAGGCAGAAGGAT	9873
rs572410425	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73088024	AGCTAGGACTACAGG[C/T]ACATGCCACCACATG	9873
rs572417732	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72911975	TTCACATATAGAAAT[A/G]CTACTTATTTTTGTA	9873
rs572422383	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73026710	ACCCAAATCTCATCT[C/T]GAATTGTAATCCCCA	9873
rs572439007	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73128958	CTCACTGCAACCTCC[A/G]TCTCCCGGGTTCAAG	9873
rs572443912	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72924317	GAGTCTTGCTCTATT[A/G]CCCAGGCTGGAGTGC	9873
rs572450378	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896827	TGGATTTTTGTTTTG[C/T]TTTGTTTTGTTTTGT	9873
rs572467569	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970350	TTACAATTCTAATGT[A/G]TGAAAATTGTCTTTT	9873
rs572477396	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855600	TACCATACACACGAA[C/G]AAACGTGAAAAGCAC	9873
rs572480655	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925004	ATTACATTTTGGCAG[A/G]AAACCATTGGAGTAT	9873
rs572489305	snp	G/T	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73122149	CTTTAATACCAGAGT[G/T]TTTTGTTGTTGTTGC	9873
rs572496946	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72875389	TATTTATTTGACAGA[A/G]TCTCGCTCTGCTGCC	9873
rs572499885	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916437	CCCACTTGGGCCTCC[C/T]GAGTAGTTGGGACAA	9873
rs572501328	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110868	TGTTGGTATGTCATG[C/T]TTCCATTATCATTTG	9873
rs572504169	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962786	CACACCAAAATGATA[C/T]CACAAAGGTCCCTCC	9873
rs572519422	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73021529	ACATGAACACATAGA[A/G]GAGAACAACAGACAC	9873
rs572533645	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72876106	GGGAGGATTGCTGAG[A/C]CCAGGAATTCGAGGT	9873
rs572538612	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72909983	GGGAGGTGAGGAGCA[C/T]CTCTGCCCGGCCGCC	9873
rs572544301	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72848801	TTTTAGTTCTGGGAC[A/G]TTCAAGTAAATATAA	9873
rs572546206	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73114565	AGCCAGCACATCACA[A/G]AAGCTCACCCAAGAC	9873
rs572559177	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72856885	TTATATATACTTAGA[A/G]GACATTGCCTTCATA	9873
rs572577020	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910389	TTGTCGAAAAGAAAA[A/G]GGGGAAATGTGGGGA	9873
rs572581136	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72947447	AAGTTGTCTGACTAG[A/C]ACTAAAGCCAAAGTC	9873
rs572582477	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73022436	ACAATACAACGTCAA[C/T]ATTCCAAAGTTAATT	9873
rs572596770	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73063448	TAACAATATTAACCT[C/T]AAATGTAAATGGGCT	9873
rs572609940	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125449	GTGGCTCATGCCTAT[A/T]ATCCCAGCACTTTGG	9873
rs572616365	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995081	GGAATCAAATAATAT[C/G]TGGCCTTATGTTTCT	9873
rs572617267	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73072794	TTTTTAAGTTTCTAT[A/G]CAGATGAAATTCACC	9873
rs572642286	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014832	CTTCCAAATTGACCT[A/C]AAAAAAGAAATCAAA	9873
rs572643776	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72966492	TTTGTTATACTAATA[C/T]GGGAATTACAGCATT	9873
rs572656288	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73026388	ACTGGGAGCAAAATG[A/G]CTGACTGAGACAATG	9873
rs572669768	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73021525	GAACACATGAACACA[C/T]AGAGGAGAACAACAG	9873
rs572700540	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048286	GTACCGACACACATA[C/T]GGGACCCAAAAGTTA	9873
rs572705624	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036508	ACTGTAAAATGGGCA[C/T]AATAATGAAACCTAA	9873
rs572725381	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995603	CAACTACTTGGGAGG[C/G]TGGGGTGGAAGGATC	9873
rs572726848	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72982660	ATAAACAGGGAAATG[A/C]TAGATCAAGTTTGGG	9873
rs572732884	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72923891	TTGCAGTAAGCCGAG[A/T]TTGTGCTATTGAAAT	9873
rs572748689	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051748	AACAACAAAAAAAAT[A/T]TGAAATAAATAGTAG	9873
rs572754660	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72907872	TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC	9873
rs572756181	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104738	CGCACCCGGCTAATT[C/T]TTGTATTTTTAGTAG	9873
rs572760901	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72899671	GAGCCCAGGAGGTTG[A/G]GGCGCAGTGAGCCGT	9873
rs572771423	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125489	GAAGGGGGACTGCTT[G/T]AGCTCCACAGTTCAA	9873
rs572772395	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72973175	GAGTTCAAGACCAGC[C/T]TGACCAACATGGAGA	9873
rs572794747	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72983853	AAATGTTTGCCGCAC[C/T]TAGGGAATAATATAA	9873
rs572796897	in-del	-/GTTGTT			intron-variant	FCHSD2	GRCh38.p7	11:72961429	GTTGTTGTTGTTGTT[-/GTTGTT]TTTAATAGATGGGGT	9873
rs572808524	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72919143	AAAAATCTAAAAAGT[G/T]TCAAACTTCCCTTTA	9873
rs572810117	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73052483	TGTGAATTACTTAAA[A/G]GCTAATGCAGTGTAT	9873
rs572815010	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974055	ACCAGCAGAGTTGAT[A/T]ACAGACAGGTAAGGG	9873
rs572816824	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72867330	AGCCCTGGACTTGAA[A/G]TAAGGAGACTTAAGC	9873
rs572819762	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096904	AAGAGTGTTAAATTA[C/T]GTGAAATGCTTTTTC	9873
rs572836793	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124713	GTGAGCTGAGATTAC[A/G]CCACTGCACTCCAGC	9873
rs572846375	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72928453	ACTTTCATGTTCCCA[A/C]ATAAGTTATTCTCTT	9873
rs572850025	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72920226	AAATAGACTGGCAAG[C/T]CTGGTCAAAATAAGA	9873
rs572850276	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927888	CGCTCTACTTTAGAT[C/G]CAAGACAGGAATGAC	9873
rs572850394	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72968625	TATCCATAAATGGGG[G/T]GTTATTCTGATTTCC	9873
rs572870755	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73083920	CAGTCAGAGGATCTA[C/T]ATTCAAACCCCAGCT	9873
rs572900150	snp	A/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73132912	CATATATGTTATAAA[A/G]AACTCTTAAAATTCA	9873
rs572907596	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72966353	TTAGTAGAGACAGGG[C/T]TTCGTCATGTTGGCC	9873
rs572910160	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73094890	CGAGGCAAGCGGAAC[A/G]AACAACTGAAGCTAT	9873
rs572919145	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73066851	GATGCTGGAGAGGAT[A/G]TGGAGAAATAGGAAC	9873
rs572927269	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858808	AAATATCAGGAAAAT[C/G]GATTTGTGCTTCCAG	9873
rs572930774	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73044940	CCGGGTGTGGTGACA[C/T]GTGCCTGTAATCCTG	9873
rs572931672	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72976928	CTCAAACTATGAAAC[-/A]TTTTTTTTTTTTTTT	9873
rs572936057	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72863069	CTAGGACCGCAGGAA[C/T]GTACCACAATGCCTG	9873
rs572939568	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965474	GCTACTTCTATAAAG[C/G]CTTTTGTGACTTTCC	9873
rs572942649	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937287	AAACAAAAAAATTCT[C/T]GGCATTTCAGTTTAG	9873
rs572974790	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965972	TATAAACATCGGCAG[A/G]AAACATGATTCTATT	9873
rs572978810	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73059800	ATTCTCATCCCAAGA[A/C]AATGAAAACCCACGG	9873
rs572979179	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937781	GGATAATTTCAATTA[C/T]ACAGGGTGCTAGAAG	9873
rs572981968	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73040031	CAAAATGGAGGACTT[A/G]CGTTGAACACAATGT	9873
rs572987103	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72929845	TTTTCCCAAAAGACC[C/T]TTAATTCCTTGAGAA	9873
rs572994427	in-del	-/ATT			intron-variant	FCHSD2	GRCh38.p7	11:72864026	CTTATCTCCAACATC[-/ATT]ATTAAGCATGGTTCT	9873
rs572998014	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72897063	AATCTCCTGACCTCA[C/T]GATCCGCCCATCTCA	9873
rs573000031	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73060496	AGGAACACATTACAG[C/T]GAGAAAGTTTTCCAG	9873
rs573010256	snp	A/C			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141585	GGCAGCATTGCCATG[A/C]GCGCGCACACACACA	9873
rs573056708	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998528	CCTGGGTGACAGAGC[A/G]AGACTCTGTCTCAAA	9873
rs573057789	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73067534	TGAATAAAAAACAAT[C/T]TGAACTTCCCCTCTG	9873
rs573068103	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72958293	AAGGCTGAGGCAGGC[A/G]GATCACTTGAGGTCA	9873
rs573092524	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105260	CACAATAATGTGCTA[C/T]AAAAGGTGGTGATAA	9873
rs573092594	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73107211	AGGCATGCGCCACCA[A/T]ACCCAGCTAAGTTTT	9873
rs573098949	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959140	TCTGTATGATTCTGT[C/T]AATACTCTTTACCCA	9873
rs573099296	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73076937	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	9873
rs573104242	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999070	TCTAATACCATCATT[G/T]GAACCCCTAGATCCA	9873
rs573109802	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943717	GCACTCAGAATGATA[C/T]CTCACACTTAGTATT	9873
rs573120099	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73099608	CATACAACCGAGTAT[C/T]ATCCAGTCACAAATG	9873
rs573123412	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067201	GACATGGATGAAGCT[A/G]GAAACCATCATTCTC	9873
rs573134037	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73138101	CAATAATACAAACTA[A/T]GCAACAGCAACAGGA	9873
rs573137985	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72890829	GCTATTAAACACAAA[A/G]CTATTTTAATTCTCT	9873
rs573144638	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844608	GCTTTGCTTCCTAAC[A/T]GTCTTGCCTGTCATG	9873
rs573160220	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73068582	CTTTATATATTTTTG[G/T]TTTAAAGTTTTATCA	9873
rs573183989	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73064326	CTAAATGCCCACAAA[A/C]GAAAGCAGGAAAGAT	9873
rs573184962	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141320	CCTTAATTTGTTTTC[C/T]CTTGGGGTGGGGAGG	9873
rs573186732	in-del	-/AAAAT	0.00478562	0.0486817	intron-variant	FCHSD2	GRCh38.p7	11:73080961	CTCAAAAAAACAACA[-/AAAAT]AAAATAAAATAAAAT	9873
rs573200937	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837839	CCTGGCTGTCTGGGC[C/T]GGTCTGCTGGCTTGG	9873
rs573201152	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72922808	ACCCAATATAAGTCA[A/C]CATTTTAATAATTTT	9873
rs573217959	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73037666	ATGTTATGAATGTGG[C/T]CATTTAATCATATAA	9873
rs573219212	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140490	AAAGACATTAACCAC[C/G]AGGAGAGGTGAGCAG	9873
rs573220087	snp	A/C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73099942	TAATGAGGCCTTTCC[A/C/T]GAGCTCTAAGTTTCC	9873
rs573225008	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73069738	TGAAGAAGCAATATT[C/T]ACAGAAATGACTAAA	9873
rs573227726	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093493	GGTGTCAGAATTGAG[A/C]GCTGTCTTAGAAGAG	9873
rs573233980	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73115081	GCAGTGGCAAGGCGT[A/G]CTGAAATTCAAGTTC	9873
rs573247480	snp	A/C/T			intron-variant	FCHSD2	GRCh38.p7	11:73097960	CTAGACTTGCATAGC[A/C/T]CATGGTGCCCAGCTC	9873
rs573257117	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72851618	CATGGTGGCATGCGC[A/C]TGTAGTCCCAGCTAC	9873
rs573261273	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72845287	ATTGGTGGGTGTGGT[G/T]GCACGTGCCTGTAAT	9873
rs573270284	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73047525	AAAAATACTGGTCAT[C/T]GACAGTACCTAGCCA	9873
rs573280940	snp	C/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73030589	CCTTAACTTTGTAAA[C/G]ATGGTGGTGGTCAAT	9873
rs573286658	snp	A/T			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73142704	GCGCGCTTTCCCGCC[A/T]GCTCGCCCCGGCGCG	9873
rs573312840	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031150	ATTTGATCTGTTATA[C/T]ATGGAATCTAAAAAA	9873
rs573318709	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73036496	TTAGTTTCCTCAACT[A/G]TAAAATGGGCATAAT	9873
rs573333024	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976442	GACTACAAGCACGTG[C/T]TAATTTTTAAATTTT	9873
rs573349448	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72992108	TCACAAGCATTCTTA[C/T]ACACCAATAACAGAC	9873
rs573358915	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921518	TCCCCCATGTGAGCA[G/T]AGTGCATTTAAACTC	9873
rs573367558	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72922523	CTTAAACATTTTGTA[A/G]CAGGGATCTTTGAAA	9873
rs573422878	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72967857	AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA	9873
rs573439255	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72859563	ATGTATGTATAGGGA[A/C]AAACACAGTATACAT	9873
rs573462914	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73024704	ACAGAGTAAACAGAC[A/G]CCCTACCGAATGGGA	9873
rs573482746	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72968646	TCTGATTTCCAAAAT[G/T]ATAGTGCTGGCATGG	9873
rs573494410	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081304	AAGGGCATGGTGGCA[C/T]GCACCTGTAGTCCCA	9873
rs573501174	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72879597	ATAGAACTTATAGAG[C/G]TAAAAATATAACATT	9873
rs573518260	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915201	CACCATGAGATACCA[C/T]CTCACACCAATAAGA	9873
rs573518433	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008416	ACAAGAAGAATGGTG[C/T]TTTAATAAATGTTCA	9873
rs573532712	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72947194	TTCTTAGTTAAGGGC[C/T]TTAAACCAAGTGGAA	9873
rs573541908	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840483	GGAGAATAAACGCTC[C/T]TTAAGGCCATGAAGT	9873
rs573556982	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73072258	AATAATGGGGATCAG[C/T]ATCAACAATGATTTC	9873
rs573561114	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73081978	GAGGCTGAGGTGGGC[A/G]GATCACCTAAGGTCA	9873
rs573563616	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096465	CTGAGGCAGGAGAAT[C/T]ACCTGAACACAGGAG	9873
rs573567289	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73132794	ATGCCCCCTGCACTC[C/T]AGTCTGGGTGACAGA	9873
rs573570967	in-del	-/AAACAAAC	0.0019972	0.0315375	intron-variant	FCHSD2	GRCh38.p7	11:72855287	GTCTCAAAAACAAAC[-/AAACAAAC]AAACAAACAAACAAA	9873
rs573586129	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040900	GCTCCCCCCCCTCTT[G/T]GGTAACTATCATTCT	9873
rs573598395	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72854749	GAGTAGTCAAATTCA[C/T]AGAGACAGAAAGCAG	9873
rs573617798	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072900	TTAAAAGAGTAAAAA[C/T]AGCAAAAAATTTTAG	9873
rs573619373	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016895	GTACAGGGATTTGAA[C/T]TGAGAAGACCATTTT	9873
rs573624409	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73088502	ACTAAAATAGTAATG[A/G]AAGTTTTCTCTGGGT	9873
rs573644186	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72935293	CCCCTAAAGTAAGAA[C/T]TTTAAACAGTCCCCT	9873
rs573653718	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73096782	TCCCCAGCCTAGACC[A/G]TGTCACTACACTCTG	9873
rs573685994	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72955537	AGTAGGTGGGTGGGG[A/T]GGAGCTAAAAGTTCC	9873
rs573688174	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73041532	TGTATATGTCTTTTT[G/T]TGAGAAATGTCTATT	9873
rs573688949	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72994859	GACATATAATTCACA[C/T]ACAACAAAATTCACC	9873
rs573690027	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72964694	CAGCCCCAGGTCTTT[A/G]TGGTAATAGCCTTAC	9873
rs573707067	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72931311	GAGGTTTCACCATGT[C/T]GGTCAGGCTGGTCTC	9873
rs573708461	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72849948	AAAATGGTTGAAAGC[C/T]GGAAAAACACTTAAA	9873
rs573717143	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73088970	GGAATAGCTTTTGTA[A/C]CCTTGATGTGCATAT	9873
rs573722787	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956336	CCATCATAAAGGTGG[C/T]TGATTCAGGAGGGTT	9873
rs573728481	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72925358	TTCACTCAGCTTCTT[A/G]AATCCTACTTTAAAA	9873
rs573745789	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72887992	AGATGTCAAAACAGG[C/G]AAGAGATTATATGGA	9873
rs573746448	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72872661	TAACATTCTATTGTA[A/T]GGATATACATTAGAA	9873
rs573747204	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72892290	TGTCTACTAAGACTT[A/G]GGAGTCCAATGATCA	9873
rs573750280	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72995500	TGAGCCCTGGAGTTC[A/G]AGACCACCCTGGGCA	9873
rs573758154	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980178	CCACTTGCTAAGCAT[A/G]AAAGAGAAGGGGTAA	9873
rs573758241	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124663	CAGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC	9873
rs573771308	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72850408	TTTGAGACGGAGTCT[C/T]GCTCTGTTGCCAGGC	9873
rs573779321	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105490	CTTGGGAAGTGAAAA[G/T]GGAATAGAGAAGAAA	9873
rs573780452	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72926225	CAGTCCAGCAGACTA[A/G]AGTGGGGACTGGTGG	9873
rs573784137	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72880295	TTTGTATGGAACCAC[A/G]AAAGTCCCTGAATAG	9873
rs573793051	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72866690	GAAAATAAAGCTTCA[A/G]TAGATTGTTTTTCCT	9873
rs573819613	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72853061	CTTAGTACCTGGGTA[G/T]TGAAACAATTTGTAA	9873
rs573874221	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73064581	GAAGAATCAAACAGA[C/T]GCAATAAAAAATGAT	9873
rs573874559	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73019956	TTCTCCAAGCCCACA[A/G]CACTACTATCTAAAA	9873
rs573878399	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72917857	CATGCCATTGCACTC[C/T]AGCCTGGGTGACAGA	9873
rs573883375	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843016	ACTGTGCAGGACAAA[C/T]GTGACCATATAAAGA	9873
rs573913766	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72865265	ATGAAGAGATACAAC[C/T]CCCTCTAAATAATTT	9873
rs573947659	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990025	TATGACATACAGGCT[A/C]GACTTTCCCAGAAGC	9873
rs573961890	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73065233	AATGTAATCTATCAC[A/G]TAAACAGAATCAATC	9873
rs573963414	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72881966	CTAACACGGTGAAAC[C/T]CCATCTCTACTAAAA	9873
rs573969667	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72916820	TATGTTTTCTTTCGT[C/T]ACTTGTGCTTTCAAC	9873
rs573972316	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73100235	ACCATTCCTCTTCGC[A/G]TCCCTTCCTCCCTTC	9873
rs573975765	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73036795	ACAAATATTGTGTTC[A/C/T]CTCATAATTTTTTCC	9873
rs573979045	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028076	GAGGGGAAATGTGGG[C/G]TTGGAGCCCCCACAC	9873
rs573985763	snp	A/C	0.000235544	0.0108497	intron-variant	FCHSD2	GRCh38.p7	11:72902504	TAAGCACAAACACAA[A/C]TGAACAACACATGAA	9873
rs573997646	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882469	GTTAGATAGATGGGA[G/T]AAGTTCTGGTGTTTG	9873
rs574010385	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910628	TGCCTGAAGGCAGCA[A/T]GCTCGTTAAGAGTCA	9873
rs574029546	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72855141	AGCCGGGTGTGGTGG[C/T]GCATGCCTATAACCC	9873
rs574036838	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73068829	AAAAAAAAAAAAAAA[-/G]AAAGAAAAAGAAAAA	9873
rs574037277	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73088846	TTGGATTTTTTTATA[C/T]TTCACAAAAGATAAA	9873
rs574066565	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73004072	CGAGATAGTGCCACT[A/G]CACTCCGGCCTGGGC	9873
rs574092906	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949225	AGGCCCATGGCGGGC[A/G]GATCACCTGAGGTCA	9873
rs574097778	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72905177	TAATTTCTTCTGACG[A/G]TAATTATTGTCGGCT	9873
rs574103004	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949720	CTACATTCAATTTTA[C/T]GGTTGATAATATTCC	9873
rs574104573	snp	A/C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72853033	TTAGAAAAAATAACT[A/C/G]TTGGGTACTAGGCTT	9873
rs574104692	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73006544	ACTGTGACTACCCCG[C/G]TTTGAGCCACCCTCA	9873
rs574108431	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72861719	TGGAGCAACTGAGGT[C/T]GGGAGTTCAAGACCA	9873
rs574121111	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897676	GTTTAGACACCCAAA[A/C]CCATGTTTTCTCCAT	9873
rs574134099	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72905652	GTCCATGTGTTCTCA[C/T]TGTTCAACTCCCATC	9873
rs574155598	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889397	GGTAAATTAATGTAT[C/T]GCTGATGGAGGGCTT	9873
rs574177764	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72850375	GGCCTAGGACAGAGA[-/T]TTTTTTTTTATTTTA	9873
rs574179220	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73108718	GGACTACAGGCGCCC[A/G]CCACCGCGCCCGGCT	9873
rs574194476	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73001207	TAACCTTTTGCTCAC[A/G]GGGCAGCACTGACAG	9873
rs574223082	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73060622	TCATGCTTTGATGGA[C/T]TGTCCACTCATCCCA	9873
rs574233006	in-del	-/T	0.191461	0.24305	intron-variant	FCHSD2	GRCh38.p7	11:73003489	TAGGTCATAGAGTGA[-/T]TTTTTTTTTTTTTTT	9873
rs574238748	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72999925	CTTCCAACTCAAAAT[C/T]ACTGGCCAGTGATCA	9873
rs574240837	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73109300	TTGCATTGAATCTGT[A/G]GATTGCTATAGAAAC	9873
rs574250747	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73042238	CTGAGATTATTTTTA[A/G]ACTCTGGTGAAAGAC	9873
rs574283459	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091930	ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAGGAG	9873
rs574291902	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123379	AACAATGCATATTAA[A/G]CGGTGGTAACTCCTG	9873
rs574301584	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72992419	AAAGACTAAAGTTCA[C/T]ATGGAACCAAAAAAG	9873
rs574315182	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042838	ATTTGAGGCTTTCTT[G/T]ATTTCTTTTTCTGCT	9873
rs574319820	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72918391	CTTTTTCTTACCGAA[C/T]TGCCCTGTCTAGGAC	9873
rs574322320	in-del	-/ACAG	0.00269875	0.0366345	intron-variant	FCHSD2	GRCh38.p7	11:73139989	CAAAGGTTCTTTGAA[-/ACAG]ACAAACAGAAGTCCT	9873
rs574323643	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934637	CTGTGCTTGGCCATA[A/C]ATTTCTTAATCAATG	9873
rs574329180	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72993853	ACATGGCACTGTATA[C/G]ATATGTAACTAACCT	9873
rs574337361	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73015617	ATGATCTATTTTATA[C/T]AGATTACAATCTATT	9873
rs574342633	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73068251	ATGCCATTATGTGCA[C/T]GTTCTCGCTTGTGAG	9873
rs574355590	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885471	GTCTAGTTTGGCATA[C/T]TATGGAAATAATAGG	9873
rs574361740	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72993675	AAAAAACCAAACACC[A/G]CATGTTCTCACTCAT	9873
rs574367772	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016119	ACCAGCTTGGCCAAC[A/G]TGGTGAAAATCTATC	9873
rs574370270	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73112698	CTGTCGCCCAGGCTG[A/G]AGTGCAGTGGCATGA	9873
rs574370665	in-del	-/T	0.00159617	0.0282053	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839543	AGAGAAGTGGAAAGA[-/T]TTGCGAGCTCTCTGC	9873
rs574391775	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72886092	CTCTGGAGTTCTAAG[A/G]GGGTGTTAGAAAACC	9873
rs574395734	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73109791	AGATCTTAGAGGAAA[C/G]GCTTTCAGTCTTCCC	9873
rs574431510	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008357	AAAGAAAAGAAAATG[C/T]GATTAAGTTCATAAC	9873
rs574433509	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72889489	AAAAAACACATATAA[C/T]GCTTGAGCAAAGGAG	9873
rs574435761	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143584	AATACCTCTTCCCCA[A/T]GCCCAGGGAGGTTTT	9873
rs574448643	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023919	AAAGGTTACACACTG[C/T]ATTATTCCATTCATA	9873
rs574469971	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952393	GCAGTGGCACTATTT[C/T]GGCTCACTGCAACTT	9873
rs574482312	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878682	TGATAATATACTAAA[C/T]AGATAAAAATCTATA	9873
rs574485988	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901276	GTGGTGCGTGCCTGT[A/G]GCCCCAGCTAATCGG	9873
rs574490402	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73093980	CTTTGGAAGGCCGAG[C/T]CAGGCGGACAACTTG	9873
rs574497396	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72881157	TATACGGAATATACA[C/T]GGAACTCAAACAACT	9873
rs574497491	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72908166	GTTTATTTCACTTAA[C/T]ATAATGACCTCCAGT	9873
rs574497907	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72916624	CCAGCCTCCTTTGTT[C/T]ACTTTTATATTGGGT	9873
rs574519084	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72879150	AAAAAAAAAGATATT[A/G]CAACTCTATCCAGCC	9873
rs574520294	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009092	AAAGTCTAATGCAAA[C/T]TGAGGTTTTAATGAC	9873
rs574522559	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73101187	GAAGGAGAAACATGA[A/C]ATTTATTCATAAAAA	9873
rs574522832	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893222	GGCCAGGCTGGTCTC[A/G]AACTCCTGTCCTCAA	9873
rs574525593	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73025009	GAAGTTGGCAAGGTC[A/G]TGGAGAAAAAGAACG	9873
rs574537110	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72846324	TAGCTGGGATTACAG[C/G]TGCACACCACCATGC	9873
rs574540233	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73061300	TTGTCGCATGGTTTT[C/T]GCAAACTGCAGACCA	9873
rs574540338	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908697	CATTATTTTTTGAGA[C/G]AGAGTCTCACCCAGG	9873
rs574549620	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838544	GGCTGCCCCCCTCTT[G/T]GCTCCTAGGGTCCGC	9873
rs574555233	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72902167	AGCGTGAGCCACAGC[A/G]CACGGCCTACTCTGG	9873
rs574555742	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73102041	TTGAAGGCCATCAGG[C/T]TGAAGACCATATTTT	9873
rs574557158	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045055	AGCCTGGGCGACAGA[A/G]CAAGACTCCATCTCA	9873
rs574562461	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73028052	GAGAACCTCTTCTAG[A/G]GCACTACAGAGGGGA	9873
rs574580306	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72963334	CATTTACTACGCACT[A/G]TCTCATTTAGATTTC	9873
rs574580536	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915544	AATGTGGTACATGGT[C/T]GGGCGTGGTGGCTCA	9873
rs574586863	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025560	GGCTTAATACCTGGG[C/T]GATGCAATAATCTGT	9873
rs574604113	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73053427	ATCACTTGCTTCACC[C/T]TGGAAAAAAGTTAGA	9873
rs574619151	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73094518	TCCAGTTGTCCATCA[A/G]TGGGATCATGGATAA	9873
rs574621249	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915903	AAAAAAGAATGAGAT[C/T]GTGTCCTTTGCAGGA	9873
rs574628252	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73057688	CCAGTTTATTCATCA[C/T]CAACAAAACCCTTAT	9873
rs574636731	in-del	-/A			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143775	CATGACCAGAAATTG[-/A]AAAGGTGGAACTTCA	9873
rs574639068	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893886	TGATATATTAGTCTT[C/T]AAGTCATCTTAACTA	9873
rs574642742	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839338	CTGTGCTTTATTCTG[C/T]AGGCAAAAGAGGAGT	9873
rs574646457	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72945213	GAGATATAGACCAAT[A/G]GAACAGAACAGAGCC	9873
rs574651100	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73039210	GGATTCCTCATAAAC[C/T]TACCTCCATAACAGA	9873
rs574680163	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73046545	TTACTATAAATTATT[C/G]GTAGAAATATAAATT	9873
rs574685759	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72985792	TCTAACAATAGGTAG[C/T]ACAAACATGTTGATT	9873
rs574705317	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909527	GGAGCCCCTCTGCCC[A/G]GCCGCCCTGTCTGGG	9873
rs574716034	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72931449	AATTTTAAAAATTAA[C/T]TTAAAAAATAATTTC	9873
rs574717403	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018548	TAATCATTATATCCC[C/T]GGCTATAGCAGATCA	9873
rs574719295	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119621	CTGGCTAATTTTTTT[A/C/T]ATTTTTTTGTAGAGA	9873
rs574731624	snp	A/C	0.030665	0.119967	intron-variant	FCHSD2	GRCh38.p7	11:73045591	TACTATGCAGCCATA[A/C]AAAATGATGAGTTCA	9873
rs574733763	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72945677	CTAATATCTAGAATC[C/T]ACAATGAACTCAAAC	9873
rs574734100	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938019	GTCTCTAAGGAGTAT[A/G]TCTAAGAAGTATGAC	9873
rs574743441	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72909902	TCTGGGAAGTGAGGA[C/G]CACCTCTGCCCGGCT	9873
rs574746607	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119138	GAGATCCTGTCTCTA[C/T]ATAAAATACAAAAAT	9873
rs574747344	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039966	ATACCAAAGATGATA[C/T]GGAAATACATAGTTG	9873
rs574755611	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72986464	TCCACCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG	9873
rs574759419	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72955490	CACCACTGGCTAATG[C/G]TGATCAAGTCACCCT	9873
rs574763137	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870507	CTGCCATTCAATGAT[A/G]TTGAGTTATAAACTA	9873
rs574779987	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73127321	GTTAAAACAAAGCAC[A/G]ATCAAGGAATATTGA	9873
rs574787373	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950731	ATTTTTCATTTATAA[A/G]AATACTTAACTCCCA	9873
rs574799201	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73056201	GCGTCTTGTTAGTTT[C/T]ATCAGGACATGTCTT	9873
rs574845460	in-del	-/GG	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73114846	TCTCAAGCGGAAGGA[-/GG]GGGGGTCTTTTTTGA	9873
rs574857509	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73070720	CGTGAGCCACCATAC[A/C]CGGCCTAAATGTCAA	9873
rs574868104	snp	C/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:73035201	GTATGTATGTATGTA[C/T]GTACGTACTAAGACA	9873
rs574871653	snp	A/C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862761	GCAAAGGACCTAGAA[A/C/T]ACCCAAAACAACTTT	9873
rs574872788	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72984372	TAAAAATTATTCATC[A/C]CTACTAAGGAATGAA	9873
rs574883792	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087417	TACTGAAGAAAGAAA[A/T]GTTTTTGGGCCAGGT	9873
rs574886901	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142661	CTGCCCTCCCTCCCC[A/C]ACGCTGGGAGCCAGC	9873
rs574896162	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932287	GTTGCCCTGCATCCA[A/G]CTCTCCCTCTCACCA	9873
rs574916787	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73062635	AGCACGAGAACTTCA[C/T]GAAGCATACACCGTT	9873
rs574922301	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72949171	AAAAGAAACCTGGCC[A/G]GGCGTGGTGGCTCAC	9873
rs574930318	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035783	TGGAGTACAGTGGCG[C/T]GATCTTGGCTCACTG	9873
rs574930360	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73028187	TGTACCTGGAAAAGC[C/T]GCAGGCACTCAATGG	9873
rs574944851	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73079048	TATACCTTAATCTGG[A/G]TAATAGTTTACATGA	9873
rs574953197	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73135253	AAACACAGATACAGG[G/T]GAGAGTACAGTAGTA	9873
rs574961579	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953909	GTGGAATAGTAAAAG[C/G]CCAATATGATTAAAT	9873
rs574962366	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72848270	CCTTTATGCACAGCC[C/G]CTCTGTTCTCCCACT	9873
rs574969304	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72882260	AGCTTGGCCAACATG[A/G]TAAAACCCTGTCTTT	9873
rs574982688	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73091132	AATGTTCCATTCTAT[A/G]AGTATACCACAATTT	9873
rs574984428	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72903302	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAT	9873
rs574991279	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73065778	AGATAATAAAATACC[G/T]AGGAATCCAACTTAC	9873
rs575023805	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72919125	ATAATAATATAAAAT[A/T]AAAAAAATCTAAAAA	9873
rs575035243	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73126245	CTTGGGAGGCTGAGG[C/T]AGGAGAATCGCTTGA	9873
rs575046982	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946456	TGTTAAATGATGAGT[C/T]ACTGGGTGCAGCACA	9873
rs575063849	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73010643	ATCTGTACGATTTCT[C/T]TGGCTATGAACAGTG	9873
rs575073502	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895269	AATATACCCATTAAG[C/G]CTGGGGTGAAGAAAT	9873
rs575075919	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73123423	CATCCTTAATTACAA[A/G]TGAGAATCATATGCT	9873
rs575078748	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72961906	GATGTGTAAATGCCA[C/G/T]ATTTCGTAACAAGAA	9873
rs575098660	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72855475	AGTGAGACTCCATCT[A/C]AAAAAAAAAAGAGTT	9873
rs575106397	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110209	GCTGGCCTCACAGAA[A/T]GAGTTTAGGAATATT	9873
rs575114490	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962675	AATGTGATTTCCTAT[C/G]AAATTCTGGAAAAGA	9873
rs575115143	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72912618	GTCTGATTTTGGTAT[A/C]AGGGTAATGCTGGCC	9873
rs575124541	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002509	AAGCAGTCCCAACAA[C/T]TGATTTTCTTGAAGA	9873
rs575124792	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72889680	TTCACACCACTGCCC[G/T]TCAACCTGGGTGACA	9873
rs575132365	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72963828	CCTCGGCTCACCTCC[C/T]GCTGTGCGGCCTGGT	9873
rs575151546	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73058810	TGACCTCAGGTGATC[C/T]GCCTGCCTCAGCATC	9873
rs575155020	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73006073	CACTGCATGTGGCTA[-/T]TTTTTTTTTTTAAAT	9873
rs575160106	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72856046	TACAAAAGCACCAAT[A/G]TTTACACATTTAAGG	9873
rs575170202	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73110826	TGAACTTCCCACTTC[A/G]TACTGCTGTCGTTGT	9873
rs575172105	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002019	TTTATTTTTTAAAAT[A/G]AGTCCTTAAAGTGAA	9873
rs575185008	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73059641	AAAATTCAAGTTTTA[C/T]GTATCCTGGTACCAA	9873
rs575198579	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927313	TACTACAATGGTGGA[C/T]ACATATCATTATACA	9873
rs575214556	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73051738	AGACATTCAAAACAA[A/C]AAAAAAAATTTGAAA	9873
rs575222386	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73093985	GAAGGCCGAGTCAGG[C/T]GGACAACTTGAGGTC	9873
rs575240365	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72927805	GCCTACCATCCTGAA[C/T]AGGGTCAAGAGCACC	9873
rs575281329	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943612	GAAGTGAGAATTCCC[C/T]GGGTCAGTCTATTTG	9873
rs575308818	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73051961	CCACCAAAGATGTTT[A/G]CTTGGAAATATTCAG	9873
rs575320038	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72936741	CTTCAGTTATTGTAT[G/T]TTTAACTCCAGAATT	9873
rs575335420	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72866250	GATGGAGCAACTCTG[C/T]TCTGTTTTTTGTTTT	9873
rs575337035	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73074922	GTCCCAAGGATGGAC[A/G]GACAGACAGTGGGGA	9873
rs575363270	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72993874	TAACTAACCTGCACG[A/T]TGTGCACATGTACCC	9873
rs575372641	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022321	AAAGGAAGAAATAAA[A/G]CTATCTTTATTCATA	9873
rs575375751	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73083058	AATGAGAACTAAATG[C/T]GTGATGAAAAATTAA	9873
rs575381751	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971911	CAAAGGAACGAGAGA[G/T]AAAAGTTTGGGAGGA	9873
rs575387478	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73066231	TTGACAAACCTGACA[A/C]AAACAAGCAATGGGG	9873
rs575387943	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72993885	CACGTTGTGCACATG[C/T]ACCCTAAAACTTAAA	9873
rs575405114	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937132	AACACAATTATATAG[C/G]TGGAGGAAGACAGAG	9873
rs575419409	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72972914	AATAAAAGGATTGTA[A/G]GCTGGCACTCTTTTG	9873
rs575430585	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72957346	GTTTCATCCATGTCC[C/T]TATAAAGGACATGAA	9873
rs575472834	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72958176	AAGATGGCTTGCTTT[A/G]AATCAAGTCAGAGGA	9873
rs575486566	in-del	-/AT	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72948593	ATTATCAATAATAGA[-/AT]ATGAGTGTATTAACA	9873
rs575487368	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72924122	TTTACTTTTTTAAAA[A/G]AAGTGATAAGGTCTT	9873
rs575493204	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73085599	GAGAAATTGAAAAGT[A/C]ACCACACAAACCCAC	9873
rs575505875	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965385	CACTAAAACACAGTA[A/G]GAAACAATACACAGT	9873
rs575510812	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72950838	CCAAATGTTATCCCT[C/T]TCTTCCTGGGCACAT	9873
rs575522547	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858713	TGTACAACCCCCCCA[A/T]GACACAAGTTTACCT	9873
rs575524326	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73137256	GTAATACGGTATCCT[A/G]TTTACAACTCTATGG	9873
rs575527401	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72899587	AAAATAAAAATAAAA[A/T]AAAACAAAATAAAAT	9873
rs575533966	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898777	CTCTGTCACCCAGGA[C/T]GGAATGCAGTGGTGT	9873
rs575534322	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73126597	TAGCATCAACTAATA[C/T]GAACTTTTATAATAT	9873
rs575534429	in-del	-/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72868839	CCACATGCAGACATA[-/T]TTTTGCACAACTGTA	9873
rs575537624	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966937	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	9873
rs575537716	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72976343	GTCACCCAGGCTGGA[C/G]TGCTGTGGCAGGATC	9873
rs575549555	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73125659	GCAGTGAGCCATGAC[C/T]GCACCACTATAACCT	9873
rs575551347	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72844507	CAGCAGCAATCCACC[A/G]GCATCAGCCACCCAC	9873
rs575582594	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73130906	TATTTAAGTGTAGCC[C/T]TACTTGATCTTTTTT	9873
rs575585093	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72843935	ATCGCTTGAGCCTGG[C/G]AGGTTGAGGCTGCAG	9873
rs575609504	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73055095	GCAAGAGAATGAGTG[C/G]CAGGAGGGAAAATGC	9873
rs575614788	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73133908	GGCTGGAGAGGGTTA[C/T]GGGGAGCGACTGCTA	9873
rs575615047	in-del	-/AGACT	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72926219	GACTGCCAGTCCAGC[-/AGACT]AGAGTGGGGACTGGT	9873
rs575616958	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836932	GTTTTCACAACTTTG[C/T]TTTTTAAAATAAAAT	9873
rs575635717	in-del	-/ATAAT			intron-variant	FCHSD2	GRCh38.p7	11:73050838	TCTACTCTAAGAAAA[-/ATAAT]ATAAGACTCAGAACA	9873
rs575648714	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990862	ATAACTAAGACCAGA[A/C]CAGAACTGAACGAAA	9873
rs575651421	snp	C/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73115612	ACACGAGAGAGAAGG[C/G]AGATAGCTAGACACA	9873
rs575657192	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73006233	TTTTTAATTCCTGCC[C/T]AGACACCTTCCCTAA	9873
rs575677214	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72946317	AACCAAACACCACAT[A/G]TTCTCACTCATAGGT	9873
rs575680488	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72991462	GATGCAAAAATCCTC[A/C]ATAAAATACTGGCAA	9873
rs575695550	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840334	AGCTAATAGGGGTCA[A/G]GGAAAATAAAATTGC	9873
rs575697957	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72851903	TTTTTTTGAGATAGG[G/T]TCTTGCTCTGTTATC	9873
rs575703037	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73036799	ATATTGTGTTCACTC[A/G]TAATTTTTTCCTCAA	9873
rs575709880	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73095650	CAAAACTCAAAGCGG[A/G]AGTACCTTTGTACAA	9873
rs575716506	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998467	GGATCACCTGAGCCC[A/C]AGAGGCAGAGGTTGC	9873
rs575731166	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72983566	TAAGAGATACACTAT[A/G]AAAATATATTTTTAA	9873
rs575758887	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72928867	CCTAATGCTATCCCT[C/T]CCCCCGTCCCCCACC	9873
rs575773036	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72890673	AGTGCTTCATATAAC[C/T]TTTTTTTTTTTTAAC	9873
rs575782584	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72988134	CTTACTGGTCTGTTT[C/G]TACAGGTGTTCAAAG	9873
rs575811555	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72891713	CTTAGTTTGAATCCA[C/T]TGTATGCCATTTTAT	9873
rs575813937	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73119099	TCAAGCTTGGGAGTT[C/T]GGGGCTATCCTGGGC	9873
rs575833800	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73088378	TGTACTCCATGATGT[C/T]CACACAATGACGAAA	9873
rs575834303	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141378	CGCCCCGTGGGAAAA[G/T]CAGGCCAAACCCTAA	9873
rs575845630	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72985469	CCATACAACTTCATA[C/T]ACTTTAGTTCCTGCA	9873
rs575845861	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73026267	ACAGGCATAAGCCAC[C/T]GTACCCAGCCTATAC	9873
rs575853666	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73075916	TTGAGTCCAGGAGTT[C/T]GAGACCAGCCTGGGC	9873
rs575883281	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72949187	GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	9873
rs575895017	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72884133	GACAACTTGATATTA[A/T]GATTCTTTATGTGAT	9873
rs575895018	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140593	TGCCTGAATCGACTA[C/G]ATAAATTACTCCATA	9873
rs575900591	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72979187	AAAGCAGTGTGAAAA[C/T]GAACTAATACAACAG	9873
rs575908483	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73023040	ACCTCACGAGTTACA[C/T]AAAAATTGGCTCAAA	9873
rs575914492	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067668	ACAAGTGCAAAATCA[C/T]CAGACAGAGAAGGAT	9873
rs575920168	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72922384	GTATATGTATATTTA[A/C]TGAACAGCAGTGACA	9873
rs575937539	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72970496	AAAAATCAAAGCTAC[G/T]TTAGTGGCATTTTAG	9873
rs575941234	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72847413	ATTTACTAATGACCT[A/G]CTACGTGCTGGGCAT	9873
rs575941740	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980128	GAAGCTGTCTTCCAA[A/C]GGTTTCTATCGTCTC	9873
rs575949132	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857223	AAAGCATGTCATCTC[A/G]GAATAATTTCTTCCT	9873
rs575992720	snp	A/C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72847988	TGAGCCACCATTCCC[A/C/G]GCCAACTCTAACCAT	9873
rs575993117	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841159	GGTGACAGAATAATA[C/T]CCTTTGTCCAGAAAA	9873
rs576002545	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73110693	GATCTTTATTATTTC[C/T]TTTATTCTACTAATT	9873
rs576003551	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73023351	AACAGTAAGAAAAAA[A/G]TCAACACATTTTTAA	9873
rs576020584	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73085221	AAACGAAGACTAAGA[-/T]TTTTTTTTTAAATGT	9873
rs576022177	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971153	TGTCATGCAGAGTAA[C/T]ACTATAAGTAACTGG	9873
rs576040979	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72939900	TGGGATTACAGGCAT[A/G]AGCCACCATGCCTGG	9873
rs576063958	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104004	TACTAATACAAAAAT[A/G]CAAATAAATGTTTTC	9873
rs576065710	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73040246	CCAACCAACCCAGCT[A/C]TTTTCCCAGGAACAG	9873
rs576110390	in-del	-/A	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72883052	TGCAAAGGTAATGGG[-/A]AAAGCATACTCTTTA	9873
rs576112122	in-del	-/AAAAG	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72949483	AAAAGAAAGGAAAGA[-/AAAAG]AAAAGAAAAGAAAAG	9873
rs576128246	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72932439	ACCACATTATCTGAA[C/T]TTGGCATACCTCTTC	9873
rs576163823	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893674	TTAGCTAGGCGTGGT[A/G]GCGCCGGAGGTTGCA	9873
rs576166566	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895059	GAAGAGGAGTGGAAC[A/G]GTGCCTCTTAAGAGA	9873
rs576174262	in-del	-/GG	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72879973	ATCGCATTCCAGCCT[-/GG]GGGCAACAAGAGTGA	9873
rs576174859	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73138465	CACGGGATCTTCACT[C/T]ACACACTAATTCTGC	9873
rs576174911	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73002438	GCTCTCCATGGCCTC[A/C]CTGCATGACAACCAA	9873
rs576193202	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72909047	TTTTTCCACCTCTCC[C/G]TTCCCCTCCCCCCTC	9873
rs576224675	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73080314	AAAAAAAAAAAAAAA[A/G]AAAAAGAAAGAAAGA	9873
rs576235341	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73137866	AAGCCAGGAAAGGAA[G/T]CTTGCAGCTGGGTTG	9873
rs576237610	snp	C/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:73003967	CAAAAATTAGCCAGG[C/T]GTTGTGGCTGGCACC	9873
rs576251762	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72887005	CCAAATCTTCCCTAT[A/T]CTTAAAAGCCCAGCT	9873
rs576253426	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72895905	TATGAGACAACGCTA[C/T]ATGCAATACAAAATT	9873
rs576253610	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73118723	TACTATAATGATGAT[A/G]GCAAACACTAACTGA	9873
rs576289180	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72925989	TCCTGGGGGAGGGCC[A/G]GGAAGGGCCCCCTGC	9873
rs576289344	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73071473	GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATTG	9873
rs576292668	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72888811	TTTTTTGTAGACACC[A/G]GGTTTTTTGCCATGT	9873
rs576296226	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72872501	ACTTTCTGTCTATAA[A/C]GATTTGCCTATTCCA	9873
rs576316160	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73018865	TGGGTATTCCAAAGC[A/T]GTTTTTAAAAATAAT	9873
rs576326599	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73053486	CTTTTAAATCTAAAT[C/G]TCTTCAGTTCACAGC	9873
rs576342445	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73033622	AAGCATATCCACACT[A/C]CCAAACCAGGATAAA	9873
rs576346878	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72994204	TTCCCTACTGGCAAA[C/T]TGTGTTTCCTGTACT	9873
rs576354205	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72962950	CTGGAGCCAGACTGG[C/T]TGAGTTCAAACTCCA	9873
rs576374900	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910047	CACCCCGTCTGGGAA[G/T]TGAGGAGCACCTCTG	9873
rs576376412	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72889306	AGGGATGAAAACTTA[C/T]ATTAATTCAACATAT	9873
rs576379602	snp	G/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:73072234	AGAAACAGAAGGTTT[G/T]GGGAGGAAAATAATG	9873
rs576404050	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73019605	ATAGACAAACAATGA[G/T]ATCTTTAGATGAAAG	9873
rs576405474	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72954887	ACATATACACACACA[C/T]ACACAGATATATACA	9873
rs576427059	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72975013	GTTATATACGCCTAC[A/T]TATGAATGAGGAAGA	9873
rs576436877	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72916489	GGCTAATTTAAAAAA[A/T]TTTTTTGTAGAGATA	9873
rs576447405	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73014863	TTCTTTTTTTTTTTG[A/G]GCTGGAGTCTCACTC	9873
rs576447410	snp	A/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72868908	TTACCTTTTTTTTTT[A/T]AATTTTTTATTTTTT	9873
rs576448096	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73026850	TTTGGCACTTCCCCC[C/T]TTGCTCGCTCTCTCT	9873
rs576460160	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73055007	TGGACTGTGGTTCCA[C/T]GTGGCTGGGGAGGCC	9873
rs576464772	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011605	CTTAGTTCTCAGAGC[A/G]TGTGTGGGACCCAGC	9873
rs576473191	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72847427	TACTACGTGCTGGGC[A/G]TTGTCCTAGGGGCTG	9873
rs576473215	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72885974	GCCTGTTCTGATTCA[G/T]ATCACTTCCATGGGG	9873
rs576498751	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73129500	AACTGCACATGCAAG[A/G]GATCTAGGTTGCATG	9873
rs576506958	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73012707	GTCATTGTATAATTC[G/T]TCATCTCTCTCCCCC	9873
rs576509146	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73104819	TGATCCGGCCTCCCA[A/G]AGTGCTGGGATTACA	9873
rs576523348	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72956167	AGAGTAACAAATTTC[A/G]ATCCATTGAATAAAA	9873
rs576524214	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72917078	CAACCTCCACCTTTC[A/G]GGTTCAAGCGATTCT	9873
rs576536572	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72863794	ATTTACAACATCACA[A/C]CTATTAGAATGTCTA	9873
rs576536593	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72845208	GGTGGATCACTTGAG[C/G]CCAGCAGTTTGAGAC	9873
rs576543509	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73048426	CTGTGTATGGACCAG[C/T]TATTGCTGAATCAAT	9873
rs576556843	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72896951	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	9873
rs576559024	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72860718	GGCGTGGTGGTGCTG[A/G]GAGGCTGAGGCATAA	9873
rs576559561	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72910461	TAGACATAGGAGACT[C/G]CATTTTGTTCTGTAA	9873
rs576568698	snp	C/T	8.23771e-05	0.0064173	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72849829	TGGAACTGCTGTCAT[C/T]GAAAACATCCATGTT	9873
rs576571316	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73007382	TCCCAGCATTTTGGG[A/T]GGCTGAGGCAGAAGG	9873
rs576578276	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72901491	TAGATTAATGATGTC[A/G]GGGGCTGAGGTGAGG	9873
rs576579319	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73128902	TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG	9873
rs576579386	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841815	ACTGATTTTAGTTTA[A/T]CTTAAACAGTTATCA	9873
rs576582329	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73113676	GCTTGTTTGTACCCG[C/T]CCTTCTTGGGAAAGT	9873
rs576584432	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73046464	ATTAGATATCATTTT[C/T]GGCCCAGGATGGCAA	9873
rs576586250	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73011442	CCAGCAGCACTTACA[A/C]TGCTAACCTAACAGT	9873
rs576590259	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73105429	CTACCAGGCTCTTTA[A/T]TTGGTAACATTACTT	9873
rs576598640	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72958214	TGGAGCTAAGGACTA[C/G]AGTGCAAAAGTGACA	9873
rs576622316	snp	C/T	5.63037e-05	0.00530553	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842886	AAGATAATTAACAGC[C/T]GGTTGCTTTTGCAAC	9873
rs576623240	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73049276	TAGTAAAACTTTAAG[A/G]AAAAAATTAAAACAT	9873
rs576625989	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72897591	CCATGGAAACCAAGG[A/G]ACAACTGTTGTCATT	9873
rs576632519	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73008236	CCCAGCTACTCAGGA[C/G]GCTGAGGCACAAGAA	9873
rs576649525	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73044139	ACATCCAAGGCCTGC[C/T]ACTATATGTCACCTT	9873
rs576649832	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73120294	TTATAATGTAGCATA[C/T]GGTCTTTATGTAAAC	9873
rs576651463	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73097924	AGCGATCCTCCTGCC[C/T]CGGCCTCCAACTGGC	9873
rs576660667	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72954426	GCCCAGGATGATCAC[-/A]AACTCCTGGGCTCAA	9873
rs576662910	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72992443	AAAAAAGAGCCCGCA[C/T]TGCCAAGTCAATCCT	9873
rs576665379	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73074326	AGAATAAAACTCTGT[A/G]TGTGCAAGGACTTAT	9873
rs576687650	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72901148	CGTAATGCCAGCACT[G/T]TGGGAGACTAAAGTG	9873
rs576688613	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73057801	CCACAGCTATACAGG[A/G]AATGAGTTCCCCTCA	9873
rs576690046	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73135391	CACCTGACTAAAATT[C/T]AATAATTTTTCCATA	9873
rs576696627	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72962507	TCACTGTAAAAAGAA[A/C]AGGAGTTTACAAAAT	9873
rs576702377	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73098578	TGTTTACAGTATGGT[C/T]AGTTGGAATAGAATT	9873
rs576716654	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73030205	CTATGTATATGTATG[C/T]GTGTGTGGGTAATCA	9873
rs576717520	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72989130	ACAATCATTATGATT[A/T]TAGTTTTCAGGCTTA	9873
rs576724440	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72988932	AACATTTATTTGCAT[A/C]ATAATTTTCTCAGAA	9873
rs576725696	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73022453	TTCCAAAGTTAATTG[C/T]TCTCCTACATACATG	9873
rs576734182	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73027150	GAGGGCTCAGAAGAA[C/G]AGAGGAGGATGTCGG	9873
rs576750981	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075875	TGTAATCCCATCACA[A/G]TGGGAGGCCAACGCA	9873
rs576759862	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949160	TTATCACCACAAAAA[A/G]AAACCTGGCCGGGCG	9873
rs576772842	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72966199	TGGTCTCACTCTGTC[A/G]CCCAGGAAGGAGTGC	9873
rs576777702	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72893153	ACAGGGCATGTACCA[C/T]CATGCCCAGTTAACT	9873
rs576794416	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72942019	GTAACATGTAAAGGC[A/G]GTGATACAGTTTGAA	9873
rs576795170	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73057306	TGGGCACTGAGGCCA[C/T]TAGGAGAAGCAAAAC	9873
rs576801694	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73038522	CTATGCAGCCATGAA[A/G]AGAATGAAATCTTGT	9873
rs576840078	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72887725	ACATTTTGAAATAAT[G/T]ATAGACTTACTAGTA	9873
rs576850362	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73054327	AGTAAGCAAAGACAG[G/T]ACTGCCCAGACCCTT	9873
rs576861419	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72913891	AAGGACCTCTAAAAG[A/G]AGAACTACAAATCAC	9873
rs576861824	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73031350	GTGTGGTGGTGTGTG[C/T]CTGTAGTCCCAGCTA	9873
rs576861927	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73039155	CTATTCCTAAGAGTC[C/T]AGTTCAAGACTGTCT	9873
rs576878862	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72920478	GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC	9873
rs576887988	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72959189	TGGTTTCCCTGTTAT[C/T]CTTTCTTTTCCACTT	9873
rs576892488	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144433	GGCAGGAGAATAGCG[G/T]GAACCCGGGAGGTGG	9873
rs576898220	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72908020	CCATCCTGGCTCCCC[C/T]CACATCTGACTACCC	9873
rs576912979	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73016013	AGAAGTGAAAAAAAA[C/T]AATGATAGGCTGCAC	9873
rs576913973	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72921301	ATTTATTTTCTCTGC[A/G]TACAATGTGACATGT	9873
rs576923864	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73032058	AGAGAATGTGCTATA[C/T]AGTCTCAAATATTTA	9873
rs576929292	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72959836	TACTTCAAATTTCCC[C/T]GATTTTAAGTTTCTA	9873
rs576949020	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72948718	TCGCCCAGGCTGGAG[A/T]GCAGTGGCACAATCT	9873
rs576954355	snp	G/T	0.00358779	0.0422022	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143911	GTCTTGCTTTTTCTG[G/T]CTTCAAAAGTTAGCC	9873
rs576955529	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72923621	TCTTTGGTGAAAAGC[C/T]TACTCAAGTCCTTAA	9873
rs576956499	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72852899	CAGGAAGAGAAAACC[A/G]AATACTGCATGTTCT	9873
rs576962560	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73067619	GCATTTATAAGACCT[A/G]GTTCTACATTAAAGA	9873
rs576971136	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72853615	AGATGGGGTTTTACC[A/G]TGTTGCCCAGGCTGG	9873
rs577001990	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73053305	AAAAGAAATGTGTGG[A/C]TCTACAACCTATTCA	9873
rs577028778	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73068175	TGAGATTTGGGTGGG[A/G]GCACAGGCAAACCAT	9873
rs577040188	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915322	ATTAGTTCAACCATC[A/G]TGGAAGACAGGGTGG	9873
rs577040324	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73125852	CTAAGAAAAACTATT[A/G]TATAAAACACTTCTT	9873
rs577041443	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73101157	TCAAAGAACCCTGAG[G/T]TTTAGTTCCGACCTG	9873
rs577059117	in-del	-/TTG			intron-variant	FCHSD2	GRCh38.p7	11:73088050	ACATGTGGCTAATTA[-/TTG]TTGTTGTTCCATTCC	9873
rs577060083	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73030057	AAAAATCACAAAGCA[A/T]ACAAAGAAATAGGTA	9873
rs577069314	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72951769	TCTGTTATTTTCCCA[C/T]TGATTTGAGGTTTAC	9873
rs577074362	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73045041	CTCCACTGCACTCCA[G/T]CCTGGGCGACAGAGC	9873
rs577074844	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062029	GGAGACACCTCCCAG[A/T]AGGGGCCAACAGACA	9873
rs577115071	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73113570	AACGGGGTTTCGCCA[C/T]GTTGCCAAGACTTGG	9873
rs577116546	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72915801	CCAGCCTGGGTGACA[A/G]AGCAAGACTCTGCCT	9873
rs577127299	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73100040	TCCCTGACGCACCCC[A/G]GAAGGCGTGTTCTTG	9873
rs577133039	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72937839	AAAAATGATTTTCTA[C/T]AGGAAATCATGTCTG	9873
rs577134188	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73062604	ACATAAATGACCCGA[C/T]GGAGCTGAAATACAC	9873
rs577138971	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72953337	TTCCTTTTTCACAAT[C/T]TCTTTTTCAAAAAAT	9873
rs577144109	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73045434	TATATACCCAAAGGA[C/T]TATAAATCATGCTGC	9873
rs577144670	in-del	-/A	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72930591	CTCTACCAAAAATAC[-/A]AAAATTAGCTGGGCG	9873
rs577153417	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72944500	GGCACAAGACAGGGA[A/T]GCCCTCTCTCACCAC	9873
rs577155394	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72952231	ATATATATGGCCTAT[A/G]AAGGAAAACACTAAT	9873
rs577160481	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72993522	CCCAAATGTCCAACA[A/G]TGATAGACTGGATTA	9873
rs577174857	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838075	CTCCTTTCTATTAGT[C/T]TATGTGATGAACAAG	9873
rs577175883	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72930610	ATTAGCTGGGCGTGG[C/T]GGTGCCCATCCGTAG	9873
rs577176316	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72938814	TCTTATCAAGCTAAC[C/G]CAAGACTAATTTATC	9873
rs577181480	snp	A/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73041630	GTTGAGTTTCTTATA[A/T]ATTCTGGATATTAGT	9873
rs577193472	snp	C/G	0.00993419	0.0697739	intron-variant	FCHSD2	GRCh38.p7	11:72945118	GCCAAAAGAACAAAG[C/G]TGGAGGCATCACACT	9873
rs577209182	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72961891	ACTCTATTTCAACTC[A/G]ATGTGTAAATGCCAC	9873
rs577234184	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73109647	CAAATCATCTGCAAA[C/T]AAGCATAATTTGACT	9873
rs577242230	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72885995	TTCCATGGGGCTGTA[A/C]CAAAAACATGCTCAT	9873
rs577246115	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73042194	AGCCTCCCAGTGTTG[A/G]GACTACAGGCATGCG	9873
rs577248812	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73093561	CAAAATCCCTAAGAA[C/T]GTTCAAATTACCAAT	9873
rs577266853	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73018883	TTTTAAAAATAATAG[-/A]AGTTTATTCCATACC	9873
rs577278520	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72878582	GTATTCAAGGACTAA[C/T]GGGGGTAATGTCAAA	9873
rs577287749	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838534	TAGGCATGAGGGCTG[C/T]CCCCCTCTTTGCTCC	9873
rs577293793	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72984609	TGTGCCAGATGAACT[A/G]CATGCTAGTTTGAAG	9873
rs577306022	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035166	TATGTATGTATGTAT[G/T]TATGTATGTATGTAT	9873
rs577335896	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72879577	GAAGATAAAAGAAGA[A/G]CCACATAGAACTTAT	9873
rs577360999	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72968735	TATACCCCATGAGCA[C/T]AAGGCCTGCTTACAG	9873
rs577366815	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73135314	CAACAATATAATTCA[C/T]TTCATTTCACTGTGC	9873
rs577373995	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73086312	TACTCGGGAGGCTGA[A/G]GCAGGAGAATTGCTT	9873
rs577384747	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73025507	GGTGGAGGGTGGGAG[A/G]AGGGAGATAATGAGA	9873
rs577386367	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73128483	GCATATGACGCAAAC[A/G]CAGATAATGAAATAT	9873
rs577396434	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72910360	GAGAACGGGCCATGA[C/T]GACGATGGCGGTTTT	9873
rs577402285	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72960996	GTGGTTGCAGAGTAG[A/G]GTAAATAGAAAATGG	9873
rs577404829	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73072992	CTTTAAGCAAGGAGC[C/T]GCCCTTAAAGTCCAC	9873
rs577423911	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142481	CGGGGTTCGAGGGGC[C/T]GGTCCGGGCTGCCAG	9873
rs577426379	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73134501	AGAACATCCATAAAC[A/T]GACCTTGGAATCCAA	9873
rs577449708	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73127303	AAAAAGATCAAATGG[A/T]ATGTTAAAACAAAGC	9873
rs577450556	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73127406	CTCCCGATCAACACT[A/G]ACAGAACATCTGCAG	9873
rs577463372	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72909185	GGGATTGCAGGCACA[A/C]GCCGCCACGCCTGAC	9873
rs577466780	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72870440	TTTTCCAAGAAAAGA[C/T]TGAATAGGCTCTACC	9873
rs577467829	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73073930	AAAGATTCAAACCAA[G/T]TCCAATCAAAATATC	9873
rs577487802	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142018	AAGACTTGCCCCGGA[C/G]GGAGCAGGCCAGCGG	9873
rs577522803	snp	A/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72941242	CTTGTTCACTATGTG[A/T]CCCCAGTAAATGACA	9873
rs577528461	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72862547	GCAAGATCTATCTAC[C/T]GAAAACTACAAAACA	9873
rs577528498	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73122342	AGAAGAAACATCAAG[A/G]CATAGACTCTGCTGC	9873
rs577530253	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73066069	CTGGGCAAGAAGAAC[A/G]AAGCTGGAGGCATCA	9873
rs577536496	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956500	ATCAACAGGTTATTA[C/T]AATCAACTTTGACTT	9873
rs577542402	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73113681	TTTGTACCCGTCCTT[C/T]TTGGGAAAGTTTTCC	9873
rs577570736	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73089145	TCATTATAATGTATC[A/G]TATATATATCAAGAG	9873
rs577575003	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72957105	AATTACATATGTATA[C/T]ATGTGCCATGCTGGT	9873
rs577575028	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72949366	GAGACAGGAGAATCA[C/T]TTGAACCCTGGAGGC	9873
rs577591618	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73009233	GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC	9873
rs577597121	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73066794	TGAGATATTATCTCA[A/C]GCCAGTTAGAATGGC	9873
rs577603257	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72948394	TTTTTCAACATTTTA[G/T]TTGCTTTCCATTTTT	9873
rs577636492	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72889257	TGAGCCACCGCGCCC[A/G]GCTATAATTATGTCT	9873
rs577639281	snp	C/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72881066	ACTCTATGCAGCAAA[C/G]GAAACAAAAGAGTTA	9873
rs577644520	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72934413	TCGGCTCACTGCAAC[A/C]TCCACCTCCTGGGTT	9873
rs577668910	in-del	-/TTT	0.00257532	0.0357915	intron-variant	FCHSD2	GRCh38.p7	11:73018518	GTACAGATCTTGTCT[-/TTT]TTTTTTTTTTTTTTT	9873
rs577671110	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72881812	ATGTTCTCACTCATG[C/T]GTGGGAGCTAAAAAA	9873
rs577677140	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72971317	TGAAGACTGCTGAAG[C/T]AGACAGAACTATAAA	9873
rs577690532	snp	C/T			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140841	CCGGGGCCCCAGGGT[C/T]CGAAGTTAACGGTCA	9873
rs577702522	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73132449	AGCTAATAAGCAGCA[A/G]AGCTGGGTTTCAATC	9873
rs577718262	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73028115	CACAGGGGCACTGCC[G/T]ACTGGAGGGGTGAGA	9873
rs577719179	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72859618	CAGGCATGCACTGGA[A/G]GTCTTGAAATATATC	9873
rs577724524	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73117505	TTAAGAGCTATAAAT[C/T]TCCTTTTGAATCATA	9873
rs577731692	snp	A/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72950749	TACTTAACTCCCACA[A/T]TATCATTTGGCTTCT	9873
rs577753969	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73091484	AACCCGGGAGGCAGA[C/G]GTTGCAGTGAGCCGA	9873
rs577764138	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73115910	GCCTTCATGGCAACA[G/T]GTAGATTAACATTTG	9873
rs577784320	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980232	AAAGTTGAAATAACT[A/G]TTAAAAATAGTAGGA	9873
rs577785694	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73020409	TTGCCATTAGATGGC[C/T]CTTTAAAATTTTTGG	9873
rs577786257	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73124584	AACATGGTGAAACCC[C/T]GCCTCTACTGAAAAT	9873
rs577787034	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73047055	TAAAAAATACTATTA[A/C]ATATAAAAGACAAGA	9873
rs577797281	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72972566	TATAAAGATTCCATG[C/T]AGGAGTTTGTTTTAA	9873
rs577803952	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72964729	ATTCTTGCTATTAGT[A/G]TCTGCCTTTCATATT	9873
rs577821689	snp	A/C	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73092034	AATGAGACTCACTCT[A/C]AAAAAAAAACAAAAC	9873
rs577825018	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72980892	GAGGCTCTTAAATGT[A/G]TATGATTAAACCAAC	9873
rs577827269	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72904520	TTTCATCTTTAAGCC[C/T]ACCTACCTCTTCCAC	9873
rs577831994	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72969607	GAAGCATCGAAGATA[C/T]AAAAAACATTAAAAG	9873
rs577846045	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73081716	TATCACAGACTTTCA[C/T]CTCAATTTTATAAAT	9873
rs577863266	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72911659	GTCCTCTTCAATTTA[C/T]TCCTTCCTTCCTTTT	9873
rs577864620	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836732	ACCTTTCTATATTAA[A/C]ACTTAGAAAACATAA	9873
rs577866082	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72865414	AAAGATGCAGGCTCC[A/G]TAAGAGTGATGAGGG	9873
rs577869126	in-del	-/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837841	GGCTGTCTGGGCCGG[-/T]TCTGCTGGCTTGGGA	9873
rs577872080	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73016348	CAACCAACCAACCAA[A/C]CAAACAAACAAAAAA	9873
rs577877994	in-del	-/AA	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:73076954	CTCTACTAAAAATAC[-/AA]AAAAAATTAGCCAGG	9873
rs577879890	in-del	-/ATAGATAAG			intron-variant	FCHSD2	GRCh38.p7	11:72846088	TAGATAGATAGATAG[-/ATAGATAAG]TAGTTACGATTACTT	9873
rs577889963	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72982739	GGACAGACATCTTCA[C/T]ATAGCTACTGAACAT	9873
rs577890569	snp	A/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839707	GAAGGGAACATAACT[A/C]ATTTTTGCTGAGTTT	9873
rs577892758	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72912482	TACATTCCACTTGGT[A/C]ATGATGAATAATCTT	9873
rs577894014	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73007283	TATCATATAAGATAT[A/C]TAGGAAAACCTAGAA	9873
rs577895665	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73138678	CAGTGGTGCCATCTC[A/G]GCTCACTGCAACCTC	9873
rs577899514	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72857905	GGGTCTGGCCAACTT[A/G]GGTTTGAATGTTGAC	9873
rs577901486	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72905696	ATGCAGTGTTTGGTT[G/T]TCTGTCCTTGTGATA	9873
rs577917798	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73077284	ACCACAGAATATATA[C/G]AGATGGCAAATAAAC	9873
rs577926829	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72983527	TAGTTGTGGCCAAAA[C/T]TGTAGTTAATAAAAA	9873
rs577928643	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72974163	ATAAACAACAGACGT[G/T]TATTTGGTTCATGGT	9873
rs577950281	snp	A/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72858590	TGGACACATAGAGGG[A/G/T]ATCAACAGACACTGG	9873
rs577955608	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73121234	AGAAGATTATTTGCT[C/T]CTGCTTATTCCTCTC	9873
rs577958549	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73071679	GCACTCCAGCCTGGC[A/G]ACAGAATGAGACTCC	9873
rs577984504	snp	G/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:73012938	TGATTTCTGCTACAA[G/T]TTCCTTGGTTCAAAT	9873
rs577998859	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73050749	ATTCACTAACATGAG[A/G]AAAAAACCGTCTCAC	9873
rs578010128	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72859367	TGGCCATCTCGGTTA[C/T]CCCAATTGACTGTCA	9873
rs578014184	in-del	-/TTT	0.0821764	0.185298	intron-variant	FCHSD2	GRCh38.p7	11:72850058	TATGAAAGAATAGAG[-/TTT]TTTTTTTTTTTTTTT	9873
rs578017680	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73106980	TACCACCAGATATCC[C/T]GGACTCGACTTTTTA	9873
rs578020336	snp	A/C	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72997769	GCAGTGGCACGATCT[A/C]GACTTCCTGCAATCT	9873
rs578039780	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73069633	AAAGAATTAAAAATA[C/T]GTGAAAAAACCAAGA	9873
rs578054597	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72998376	GAAACCCTGTCTCTA[C/G]TAAAAATACAATAAA	9873
rs578077615	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72943584	TGAGACGGAGATGAA[A/G]GGCACAGAAATGGAA	9873
rs578088788	in-del	-/TTCT	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72932175	TCTTATTGATTCCAC[-/TTCT]TAAATATTTACCAAA	9873
rs578099122	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72990753	TGCCCACAAGAGAAA[A/G]CAGGAAAGATCTAAA	9873
rs578101036	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72935831	ATAAGGAAGTTTATG[C/T]CTGTAAATTACAAAA	9873
rs578116833	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72898680	CTTTTCTGGCTCTAA[C/T]GCTTATTAGCTGAGT	9873
rs578135426	snp	A/C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73104715	CTGGGACCACAGGCA[A/C/T]GTGCCACCGCACCCG	9873
rs578153226	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72912325	TATGTTCCCTCTATA[C/T]CCAGTTTATTGAGGG	9873
rs578162307	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73100467	CTCCTGGGTTCAAGC[A/G]ATTCTCCCGCCTCAG	9873
rs578173534	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084178	GATGTTTACTGGACT[C/T]AACCAATGTAAGAGG	9873
rs578176228	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72899441	AGAACCACGAGATAC[G/T]ATTTCATATCCACTA	9873
rs578179442	snp	A/T	1.69522e-05	0.00291132	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72889930	TGGTCCCAGTTTCTG[A/T]TTCTAACTGTCGGCT	9873
rs578188928	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73029412	CCAGAGAAAGATTTG[A/G]AGAGTAAATTACAGT	9873
rs578190058	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73043662	CAAGGCATATACATA[A/G]AAGAAATTTTCCAGC	9873
rs578191374	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73035961	CTTGACCTTGTGATC[C/T]GCCTACCTCAGCCTC	9873
rs578194087	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72876222	GTAGTCCCAGCTATT[C/T]GGGAGGCTGAGGTGG	9873
rs578209399	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73084819	CAAACATAGGCATTG[G/T]AGAGTCAACAAAATG	9873
rs578212525	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73130121	TCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA	9873
rs578215301	snp	C/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73075057	ATATGAAAAGTTCCT[C/G]TAATTCATTAATCAT	9873
rs578235393	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73108952	CATTCTTCTGCATAC[A/G]GATATTCAGTTTTTC	9873
rs578245548	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72928640	TTCTATGTGCTGTAT[A/G]GGTATTATTGCCAAT	9873
rs578250873	snp	G/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73092816	CATCGGAGTATACAG[G/T]AAAGGATTAACCCTA	9873
rs745308193	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72928254	GGAAAAAAAATTCCA[C/G]AAAATTTTTTTCAAT	9873
rs745310383	snp	C/G/T	0.000162995	0.00902633	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838917	TCAGTCAGTTCCTGA[C/G/T]TCAGTATCTGAAGCA	9873
rs745313133	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72903240	ATTTATTTTTTGAGA[C/T]GAGTCTCGCTCTGTC	9873
rs745314714	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73138997	ATTGTAATTTTCAGT[C/T]AGAAAACAACAATCT	9873
rs745317990	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73090957	CCTGTCAACTACTAA[A/T]CTAATTTTTTGTCTC	9873
rs745334765	in-del	-/TTTATTTA			intron-variant	FCHSD2	GRCh38.p7	11:73035696	CTGAAATGTTCAGTT[-/TTTATTTA]TTTATTTATTTATTT	9873
rs745341056	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73100829	CTCTTTCCCAAATAC[G/T]GGGCATTCCTTTTTT	9873
rs745341664	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72892266	AGAGCTTTTCCCTTA[C/T]TTTTTATGTGTCTAC	9873
rs745343426	in-del	-/TTTG			intron-variant	FCHSD2	GRCh38.p7	11:72892597	TTATGTTTTTGTGTT[-/TTTG]TTTGTTTTGTTTTTT	9873
rs745343898	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72848159	CTTCTTAAAAGTCCA[A/G]TCTGATTTCAGGCCA	9873
rs745363284	snp	C/T	5.66524e-05	0.00532194	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867945	CCATTACTTGGTTCA[C/T]GGCACTCTTTAGCCA	9873
rs745373823	in-del	-/AT			intron-variant	FCHSD2	GRCh38.p7	11:72884585	TATATATAAAAGATC[-/AT]ATATATATATATAAA	9873
rs745394107	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73073825	ATAAAAACTGTACAT[A/G]TGCAAGGATTTTTTT	9873
rs745395795	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72879594	CACATAGAACTTATA[A/G]AGCTAAAAATATAAC	9873
rs745404124	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73022619	GATGGAGAGACATTC[C/T]ATGTTAATGACTTGG	9873
rs745413421	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73125593	ATCTGTAGTCTGAGC[C/T]ACTCAGGAGGCTGAG	9873
rs745415736	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72969441	AAAGAAAGAGAAAAA[C/T]ACTGAGAGGGACAGA	9873
rs745422990	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72930140	CAATTGAGGGGCCAG[A/G]AGGAAAAAGCACTTA	9873
rs745428864	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73132221	CATGAAACACGATAA[C/T]TTCCTTTTGTACCTT	9873
rs745450412	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72859312	CCCCTTTGTCGAGTA[C/T]ATGCAAGCTATGTAA	9873
rs745474324	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72999706	AAGCACCAGAGGTAG[G/T]TAAACTCTCTAAATA	9873
rs745477329	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73104386	CTTCTCTTGCCTCAG[A/C]CTCCTCCAGAGTAGC	9873
rs745485009	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72891002	GGCTCACTGCAGCCT[A/C]AACCTCCGGGCTCAA	9873
rs745505072	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841765	CCAATTTTGCATTGC[A/G]CTTCACTTTTTCCTC	9873
rs745518805	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72874279	GCAGCCTCGAACTGC[G/T]GGGCTCAAGTGATCC	9873
rs745524855	snp	C/T	1.6585e-05	0.00287962	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840903	TGCCATATGAGGTCT[C/T]AGGAGTATGCCTTGA	9873
rs745533675	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72981155	TTAATGTACAGTACA[C/T]GAAAACTGAAAGTAT	9873
rs745543789	snp	A/G	1.78551e-05	0.00298784	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73001083	ATTCATCCGAGACTG[A/G]GCTACCTGCATTGTT	9873
rs745549602	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73001982	TATAAACACAATCGA[C/T]AATTTATAACAATGG	9873
rs745563864	snp	C/G	0.000131852	0.00811842	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72887472	GCTGCCACCTTACCT[C/G]TGCTTTACGAATATT	9873
rs745582841	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73051239	AAAATCAGTTGAACC[C/T]AGGGGATTGAGGCTA	9873
rs745593354	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72965080	AGGCATGAGCCACCG[C/T]GCCTGGCCAATCATT	9873
rs745599806	in-del	-/TTC	6.55759e-05	0.0057257	intron-variant	FCHSD2	GRCh38.p7	11:72983898	TTGTCTGTAAACATT[-/TTC]TTAACTAAAAATTAA	9873
rs745606453	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72850993	AGTCCCAGCTACTGC[A/G]AAGGCTGAGGCAAGA	9873
rs745609042	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73097798	TTTTAGTTTCTGTAA[A/G]GTAGTAGTATCCCCA	9873
rs745614790	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72954787	AGGAAGATATTTACA[A/T]ACAAACATAGAAAGG	9873
rs745622574	in-del	-/CCC			intron-variant	FCHSD2	GRCh38.p7	11:73051910	CACACACACACACAC[-/CCC]ACACACCCCACACAC	9873
rs745641459	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72994468	ACTCAGATGTTAAAT[A/G]ATTTACTCTGAGTCA	9873
rs745645162	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73048337	AAGGTTCATGATAGT[C/G]TAGTACTGGCTTGTT	9873
rs745660353	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72901773	TATTCTAAGAAATCT[A/G]AAAGGAATTATAAAA	9873
rs745661517	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73081925	AAAGCATTCAAGATC[A/G]GGCGCGGTGACTCAC	9873
rs745663713	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72980098	GTCTTCAACACAGAT[-/G]AAGTGGACAATATTG	9873
rs745674562	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72886061	CCCCACAACCAGTGA[A/C]GCACTTCCTCAAAAC	9873
rs745677352	in-del	-/TTC			intron-variant	FCHSD2	GRCh38.p7	11:73115762	GTCTTGAGGCAAAAT[-/TTC]TTCTTCTTCCAGATA	9873
rs745683935	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72999567	TCAGGTGATCCACCC[A/G]GCTTGGCCATCCAAA	9873
rs745685749	snp	A/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839572	GCAAGGTATACCTGG[A/C]AGGATTTGGGAATGA	9873
rs745696727	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73083505	AGTGAGCCAAGATTG[A/C]GCCACTGTACTCCAG	9873
rs745708763	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72855040	GCACTTTGGGAGGCC[A/G]AGGCAGGCAGTTCAC	9873
rs745718172	snp	C/T	0.000291146	0.0120619	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902562	TCACTGTCACAAGGC[C/T]GGAACTGGAAGGGCT	9873
rs745730403	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73133737	GGCGGAGGTTACAAC[A/G]AGCCGGCATCGCGCC	9873
rs745741726	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72938085	GAAATACATCCCCAG[C/T]ACCCTCAATGGCAGA	9873
rs745755939	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73130331	AGTACTATCATAGCT[A/C]ACTGTGGGCTCAAGC	9873
rs745765804	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73058482	TAACACATGATAGAA[A/T]GATACATAGTTAAAT	9873
rs745771397	snp	A/G	6.59609e-05	0.00574248	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902632	GAAGATTGTAGTCCC[A/G]GACCACCTAAAGAGA	9873
rs745774006	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72914694	ATATGCAGAAAATTG[A/C]AACTGGACCCCTTCC	9873
rs745787298	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73112174	TTCTTATAGGACAGG[G/T]CTGGTGTTGATGAAA	9873
rs745820838	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72953740	AAGATGCCGCCTTAT[A/G]TTGTGTAGTCAGGGA	9873
rs745828267	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72970305	ACACTACCAAAACCT[A/G]ACAGTCTACAATCCA	9873
rs745830695	snp	C/T	3.29652e-05	0.00405974	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843405	GACCAAAACAAACTC[C/T]TAAAAATGTCACAAG	9873
rs745841542	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72854291	ACAAATGTTCACAGC[C/T]ACATTATTCACAAAA	9873
rs745853043	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72867630	GATAGGCATCGATAA[C/T]CCAAATAGTGATAAC	9873
rs745861138	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73011037	CAGGTAGGTGTCAGC[A/T]GTGATTGTAGTGGCA	9873
rs745862596	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73041944	TATTTATTTATGTTT[C/T]TGAGACAGAGTCTCA	9873
rs745866223	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73050977	AGCATTTAGAAAGTT[G/T]TAAGCAATTTGACAT	9873
rs745875391	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72967790	TATCTAATTTTTTTT[A/T]AAAAGAAGTGGGCAG	9873
rs745880447	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73059684	GAAACCGGCTAATAA[C/T]GAATTTTACTAAAAA	9873
rs745896076	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72895875	CACAAATTCTATCAC[A/G]GCCTTTTTCACATTT	9873
rs745896145	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72912284	TCATTGTGGGTCTGT[C/T]ATACATGGCTTTTAT	9873
rs745901140	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72946146	GACTTGGAACCAACC[C/T]AAATGTCCAACAATG	9873
rs745915996	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73008221	ATGCACACCTGTAAT[A/C]CCAGCTACTCAGGAG	9873
rs745919391	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73107914	CAATCGACATGGGTA[A/T]CTTTTGGATATATAC	9873
rs745922317	snp	C/T			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143494	TGCACCCCACCACCA[C/T]ACATGAACCTTCCTG	9873
rs745926550	snp	A/G			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73144173	TCATAGGCTTACTGT[A/G]TTAAATAGAATTTCT	9873
rs745959500	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73063699	AGACAAAGAACGGTA[C/T]TACATATTGGTAAAG	9873
rs745959636	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73031416	GGGAGGTGGAGGCTG[A/C]ATTGAGTTGTGACTA	9873
rs745962873	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72942667	AATGGAAAATACATA[C/T]TTTATTAAAATTAAA	9873
rs745966128	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73056805	TAGATTGACAAGGCC[A/G]GGCGCGGTGGCTCAC	9873
rs745971826	in-del	-/GTA			intron-variant	FCHSD2	GRCh38.p7	11:72994384	GACTCTATGAAAAAG[-/GTA]GTAGTAGTAGTAGTA	9873
rs745976958	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73038958	TTTGGCTTGACTTCT[A/G]TAATGACCCCCAGCC	9873
rs746009828	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72934192	AGTTTGAGAAGGGCA[C/T]GTATGATGAAGATGC	9873
rs746010900	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73094382	ACATAATTAAACTTA[C/T]ATTTATTTTGATATA	9873
rs746012468	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73033357	CACTCTAGTCCTGTC[C/T]AAAGATGATATGCAC	9873
rs746052176	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73112863	TAGAGATGGGGTTTC[A/G]CCATGTTAGCCAAGC	9873
rs746054674	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72911308	ACTGCAGATAGGTAG[A/G]TTTGATTCTGGGTTC	9873
rs746058811	snp	A/C	1.66018e-05	0.00288108	intron-variant	FCHSD2	GRCh38.p7	11:72849907	AAGAAAAATTAGAAA[A/C]CATTGGCTAGTTTCC	9873
rs746059344	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72926401	CCAGTTGCAGAGAGG[A/T]GTATTCTCTCTGCTA	9873
rs746061284	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72882573	AAATTATAAATGTCT[A/G]AGGTGATAGATATCT	9873
rs746081521	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72876739	TTCTATATTCTTGTT[C/T]TATCAATTACTGAAA	9873
rs746082711	in-del	-/TTT			intron-variant	FCHSD2	GRCh38.p7	11:72872287	TTTTTTTTTCTTTTC[-/TTT]TTTTTTTTTTTTTTT	9873
rs746101129	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72863032	GGTTCAAGATACCTT[C/T]TTGCTTTAGCCTCCT	9873
rs746103407	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73122506	CTCTTCAGAACACAG[C/G]AATGGCTACTTGTAA	9873
rs746107271	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72966008	AAAGTAACAATGAGG[C/T]AAGAGAAGAAGATAA	9873
rs746112798	snp	A/C	2.09028e-05	0.00323279	intron-variant	FCHSD2	GRCh38.p7	11:72867857	ATATCCAAGAAAAGA[A/C]ATCGTACCGAGTGTA	9873
rs746129435	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73034613	CAGCAAATTTATACT[A/C]ATAGTAAAGAAAAAG	9873
rs746151468	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73021564	GCCTTTTGGAGGATG[A/G]AAGCTAGAAGGAAGG	9873
rs746153399	in-del	-/TTTT			intron-variant	FCHSD2	GRCh38.p7	11:73035698	GAAATGTTCAGTTTT[-/TTTT]TATTTATTTATTTAT	9873
rs746153612	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73006797	GCAGCAGAAGCTCTG[C/T]TTCATTCACTGTTGT	9873
rs746180524	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73116355	CATATAATTTGATTG[C/T]TTGTACTGTCCTGTT	9873
rs746184838	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72927093	ACAAAACAAATGTAT[C/T]TCAGTCTTGCCCTCT	9873
rs746187247	snp	A/T	1.64784e-05	0.00287035	missense, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842625	CTCTCAGGTACCTGA[A/T]TCTCTCTCATCCATG	9873
rs746194343	snp	A/G			intron-variant, synonymous-codon	FCHSD2	GRCh38.p7	11:73016545	CATGTCACAGGGAAC[A/G]CAGCTGTCCATCTCC	9873
rs746202780	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72974631	AATATGGCTACTGGG[A/G]CTGAGAAACAGAATT	9873
rs746222333	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73010761	GGTAGGCCAGTCTTT[A/G]AGCCCCAGTAGAGGC	9873
rs746238777	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73008326	CCTGGGCGACAGACC[A/G]AGACTGTCTCAAAAC	9873
rs746258410	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72858210	CAACTCCACTGGACA[A/G]AGAAGTAATCACAGT	9873
rs746266455	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73064901	GTCCAGGACCAGACC[A/G]ATTCACAGCCAAATT	9873
rs746271376	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72960812	CACTCTGATAATAAG[A/C]ATACAGGTAAAGAAA	9873
rs746280031	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73101417	AGGGAGGTAAAGGCT[A/G]TACTCTTGTTGTTAT	9873
rs746301927	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73123630	GACAATGTCATCACA[C/T]TATAATGGCAATATT	9873
rs746316730	snp	A/G			intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836515	TTTTTTTTCCCATGG[A/G]AAAAGCAAAGACCGT	9873
rs746324977	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73040290	ACTAGAAGCTGTAAT[G/T]GTTTCGCAGTCATGT	9873
rs746340521	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72987948	AAACAATAAATACAA[A/T]AAAACAAATTAGAGA	9873
rs746350196	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72917945	CTGCAAAAAAGGCCA[C/T]TGGAATTTTGATAGG	9873
rs746351724	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72863043	CCTTCTTGCTTTAGC[A/C]TCCTGAGTAGCTAGG	9873
rs746365924	snp	G/T	2.79045e-05	0.00373517	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72921904	TCAGTCCGGCTGAAG[G/T]CTATTAAATAATCCT	9873
rs746368005	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72989323	TTTGCCTAACAACCA[C/T]ACATTGAGAAATAAC	9873
rs746373190	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72883353	AAAAGTTTCCAATCT[A/C]GAAAATGAAAAGGTA	9873
rs746389436	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72973589	TCAGAGTGGTAGTTA[C/T]AATCTGTTGAACATA	9873
rs746400679	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72960077	TCTATAAAGAAAAAA[-/G]GTTTGGCTCACAGTT	9873
rs746447650	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72991089	CTATAAACACCTCTA[C/T]GCAAATAAACTAGAA	9873
rs746447753	snp	A/G	1.64773e-05	0.00287026	missense, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843220	TGGACGTGTGTGACC[A/G]ACTGTCCAAAGCGGC	9873
rs746453333	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72932141	CTGCCTTGTCCCCCA[C/T]ATACTGTTAATTACC	9873
rs746454215	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73127697	ATCATCAATTATTAA[A/G]GGGCAAATTATTCAG	9873
rs746456952	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837875	AAATAATGCCGGGGC[A/G]TCCCCAGTAGAGAAG	9873
rs746465457	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72914815	ATACCATTCAGGACA[C/T]AGGCATGGGCAAAGA	9873
rs746470535	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73073833	TGTACATGTGCAAGG[A/T]TTTTTTTTTCTTTTT	9873
rs746480369	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73025532	ATGAGAAAAAAATAA[C/T]TAATGGGTACTAGGC	9873
rs746488064	in-del	-/TTT			intron-variant	FCHSD2	GRCh38.p7	11:72938178	AGATTATGAAGGAGT[-/TTT]TTTTTTTTTTTTTTT	9873
rs746524095	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72858252	CAAATACAACATGAG[C/T]AAGTTATCAAAGATG	9873
rs746529474	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73064641	GTGGTGATATCCTTA[-/T]TATCAGTGGTGATAT	9873
rs746539896	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73113226	TCTCTGTGTTATCTC[A/G]AATTTCTTAGAGTTT	9873
rs746555667	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73060015	TATATATTCCTCTAA[A/C]GTATACCTCCTATCC	9873
rs746558175	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73104629	GCTGGAGTGCAGTAC[C/T]GCAATCTCATCTCAC	9873
rs746564626	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72915995	ACCACATGTTCTCAT[C/T]TGTAAGTGGGAGCTA	9873
rs746582575	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72848352	TCTGTCTCTATACCT[A/G]CTGTTCTCTTTGCTT	9873
rs746594006	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72900118	AATTCTTAATTTATA[A/G]GAGAAAACACAGCTG	9873
rs746595141	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72982402	CAATTCGACTACAGC[A/G]ATGTGTGTGTTTGTT	9873
rs746612703	in-del	-/AC			intron-variant	FCHSD2	GRCh38.p7	11:72999875	CAATCAGACACACAC[-/AC]ACACACACACAAACA	9873
rs746616980	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73041657	TAGTCCTTTATTAAA[C/G]GAATACTTGCAAATA	9873
rs746626503	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73077245	TTTAAAAAAAAATCA[A/G]TAAAATATTTGAACA	9873
rs746626524	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73004867	ATTTCCCAAGTTCTC[C/T]CTTCTCAAACCTCTA	9873
rs746649659	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72893195	TAGTAGAGATGGGGG[-/T]TTTGCTATGTTGGCC	9873
rs746658418	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72844934	CTCATTTACCCTTGA[C/T]AGCTTTTCCAATGGA	9873
rs746666197	snp	C/G			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140486	ATTCAAAGACATTAA[C/G]CACCAGGAGAGGTGA	9873
rs746671526	snp	C/T	1.704e-05	0.00291885	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843365	AAACAAGTTTACACA[C/T]ACAATTTAGACAGGG	9873
rs746671914	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72846919	AATTTCAGTAAGTTT[-/C]ATAATATTATATGTT	9873
rs746677663	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73125922	TGGCTAATGCAAAAC[C/T]ACATTTCACAACAGA	9873
rs746690584	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72930251	TATCTAATAGCTGCC[A/G]AAACAATCTGTTGTG	9873
rs746708450	snp	A/C	1.88386e-05	0.00306903	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72988999	CTCTCGTACTGCATG[A/C]GCCATCTGTTCAGTC	9873
rs746712636	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72880576	GATCCCTATCTCTCA[A/C]CATATATAAAAGTCG	9873
rs746716199	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72956204	TCCATGGACATAATG[A/T]TATAAATAAATAAAC	9873
rs746724931	snp	A/G	1.67301e-05	0.00289219	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838905	TTACGTAGTTTGTCA[A/G]TCAGTTCCTGACTCA	9873
rs746736841	snp	A/G	6.30524e-05	0.00561446	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841472	TTGCTGAAGGAGACC[A/G]GGGAAAGTACAGGGA	9873
rs746760902	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72887824	TGAGAGACCCCAAGG[C/G]AAACTGCTAAGCTGA	9873
rs746763642	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72939817	AGAGATGGGGTTTCA[C/T]CATGTTTGTCAGGCT	9873
rs746780734	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73134869	GTTTTTTTTGAGACA[G/T]AGTCTAGCTCTGTCA	9873
rs746803382	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72968048	GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC	9873
rs746804866	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72997755	ATCCAGGCTGGAGTG[C/T]AGTGGCACGATCTCG	9873
rs746812226	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72920040	TTACTTAAAAACAAG[-/A]AAAGACTGAAAATAT	9873
rs746812270	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72875592	CCCTCCTGCCCTGGC[C/T]TCCCAAAATGCTGGA	9873
rs746819034	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73054822	GCTAGGACTACAGAC[A/G]TGTGGGCCTGGTGGC	9873
rs746839937	in-del	-/AC			intron-variant	FCHSD2	GRCh38.p7	11:73134047	AATCATATATGATAT[-/AC]AGTCACATCATGTAA	9873
rs746843050	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72856117	GCCATTACATTAATT[A/T]ATTAAAGTATCAAAT	9873
rs746843392	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73069205	AGTCCCAGCCACTCG[A/G]GAGGCTGAGGCAGGA	9873
rs746843587	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73032291	TGGAGTACAACAGCA[C/G]AATCATTGTTCACTG	9873
rs746858855	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72869256	CCCTATCAAAAAAAG[A/G]AAATCAAGGCTTTTT	9873
rs746866405	snp	C/T	3.3873e-05	0.00411526	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73015863	TCTCTCTTCAGGTAT[C/T]GACTAGCCAACTTCT	9873
rs746868656	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73136199	AAAAAAGAAGGGACG[C/T]AATGGGGAAGAACTA	9873
rs746885224	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73012712	TGTATAATTCTTCAT[C/T]TCTCTCCCCCTGCTT	9873
rs746892598	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72924776	CACTAGATGACACCA[C/T]TGAGCACTTCAAATT	9873
rs746894251	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73055496	TCTGATAAGAAATAA[C/G]ACAAAGTTTTAAACC	9873
rs746899622	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73043376	TCCTATCCACTTTTC[G/T]GGGCAACCTGTCAAG	9873
rs746919408	snp	A/T	1.64936e-05	0.00287168	intron-variant	FCHSD2	GRCh38.p7	11:72889979	CAGAGATAAAAATAT[A/T]GCTATCCTTATTGTA	9873
rs746923631	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72871896	TGTGCCCAACAGGTA[C/T]ATAATTTTGATTTCC	9873
rs746925121	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73101134	AAACATCTGAGATAA[C/T]TGGGGTTTCAAAGAA	9873
rs746925497	snp	A/G	9.08884e-05	0.00674062	intron-variant	FCHSD2	GRCh38.p7	11:73083659	AGCCACGGAAAAGAA[A/G]TATACCTAGAATGGG	9873
rs746925641	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73061235	TTTCCCCCTACCCAG[A/G]GGAAGCCATGAGGGA	9873
rs746931270	in-del	-/T	2.72676e-05	0.0036923	intron-variant	FCHSD2	GRCh38.p7	11:72984084	GATATGAAAGCTGTA[-/T]TACCTTCATAATGTT	9873
rs746932644	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73098838	AGGGGCAATTCTTCA[C/T]GACCTTGGATTTTGC	9873
rs746975893	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72956094	GTGCTCAGAGAACAA[G/T]GGGGACATACTCCTA	9873
rs746980300	snp	A/G	7.21267e-05	0.00600484	intron-variant	FCHSD2	GRCh38.p7	11:72902530	ATGAAATGAAAATCT[A/G]TAATTCCCTTACAGT	9873
rs747005831	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72935721	TTGATATAAAGTAAA[A/G]TCAGAAACATATCAT	9873
rs747011718	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73079060	TGGATAATAGTTTAC[-/A]TGAGTGTGTTCACAA	9873
rs747017439	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73023269	AAGCTGCAGATTAGG[-/A]AAAAAATACTTGCAA	9873
rs747018165	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72898579	CATTTACCATCATAT[A/T]TAAAACTCAAAAATA	9873
rs747029278	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73095529	ACATAACTGGAAATA[C/T]GATCTCCAATAAAAC	9873
rs747033485	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72953330	TTCAAAATTCCTTTT[C/T]CACAATTTCTTTTTC	9873
rs747035903	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72938669	TGTCTGGAGAGGGTC[A/G]ATTTTCATCATTCTT	9873
rs747059598	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73131059	AGTCCAGTACCTGAT[C/G]TGCTACTTCCAGTTT	9873
rs747075817	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73037514	CAAAATTATTTTTTG[-/C]CTCTGAGTTTTTGAT	9873
rs747079073	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72954195	GCAGTAGATGTGGGG[-/A]ATTTTTTTTTTTTTT	9873
rs747082091	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72989472	CCCCATAATCTTAAC[A/T]AAGTCTCTCTTTATG	9873
rs747102767	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72884449	GGCCCAGAGGTAATA[C/T]AAATTTGGAAATAAT	9873
rs747138187	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73081392	TGAGCCAAGATGGCG[C/T]CACTGGACTCCAGCC	9873
rs747141256	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72919707	TCTCCAGTCCAACTT[A/G]TTCTTGGAAAAAAAC	9873
rs747157317	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73118659	GAGGATGTTTATCTC[C/T]TCATTACTGATTTCT	9873
rs747161380	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73022390	TACCAAAAAACCTCA[G/T]GGAACTAATAACTGA	9873
rs747177379	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73056956	GGCATGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT	9873
rs747177420	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72913466	TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC	9873
rs747227530	in-del	-/ACACACA			intron-variant	FCHSD2	GRCh38.p7	11:73051909	CACACACACACACAC[-/ACACACA]CCCCACACACACTGA	9873
rs747232164	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72897597	AAACCAAGGGACAAC[A/T]GTTGTCATTTTACAC	9873
rs747257782	snp	C/T	7.61731e-05	0.00617096	intron-variant	FCHSD2	GRCh38.p7	11:72984040	CCAACTTAAGTTGTT[C/T]TTGTTTTCAATGAAG	9873
rs747261290	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:73138606	ATCTTGCACAGGAAT[-/TT]TTTTTTTTTTTTTTT	9873
rs747276308	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73002573	GTAACTATTAATTTA[C/T]ACTTAAAATACATTT	9873
rs747279943	snp	C/T	1.65888e-05	0.00287996	intron-variant	FCHSD2	GRCh38.p7	11:72989146	TAGTTTTCAGGCTTA[C/T]AGAAAATGACTTCAT	9873
rs747280691	in-del	-/TTT			intron-variant	FCHSD2	GRCh38.p7	11:73045989	CAATAATTTCAGTAA[-/TTT]TTTTTTTTTTTTTTT	9873
rs747306146	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73002232	AAGGAAAAAACTTGA[C/T]AAACTATGGTTTTCA	9873
rs747313583	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72942642	TTTTCTTCTGGTACT[C/T]TGGTAATCAAATGGA	9873
rs747315735	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72977782	GATCTAGAACTAGAA[A/G]TACCATTTGACCGAG	9873
rs747317511	snp	C/T	1.65894e-05	0.00288	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867975	ATGTGTCCACAGAAA[C/T]ACCAATCTGCTTTAG	9873
rs747322191	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73058045	CGACCACGCCTGGCT[A/G]ATTTTTTGTATTTTT	9873
rs747324551	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72962466	GACAAAAACGTTTGA[A/G]AACCTCTGGTATAAG	9873
rs747327330	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72906807	TTGGTACCAGTGCCA[C/T]GCTGTTTTGGTTACT	9873
rs747337739	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72898480	CCTAATTCAAACTAT[A/G]AAATTCAAAATAAAA	9873
rs747347756	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73064078	AAAAGAATGGAAATC[A/C]TAACAGTCTCTCAGG	9873
rs747361345	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72860372	AGTTACCAAGATATA[C/T]GTTTATACTGGGTTA	9873
rs747382501	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72908343	TGCTGCAATCAACAT[A/G]AGAGTGCAGATATCT	9873
rs747406635	in-del	-/ATGAG			intron-variant	FCHSD2	GRCh38.p7	11:73026813	AGCAAGTGAGTTCTC[-/ATGAG]ATCTAATGGTTTAAA	9873
rs747417682	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72943460	ATCAGGAAAAAGACA[G/T]CACAGAACAATATGG	9873
rs747418406	in-del	-/CT			intron-variant	FCHSD2	GRCh38.p7	11:73038831	TGTACATGTATTCCC[-/CT]GATTCTAAAATAAAA	9873
rs747429087	in-del	-/CAT			intron-variant	FCHSD2	GRCh38.p7	11:73065799	CCAACTTACAAGGGA[-/CAT]TGTGAAGGACCTCTT	9873
rs747434588	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72847366	ATTCATTTGTTCATG[C/G]CTTCCATCATTCAAG	9873
rs747441529	snp	A/C	1.65474e-05	0.00287636	intron-variant	FCHSD2	GRCh38.p7	11:72887441	GTCATTAGACCTGGG[A/C]AAAATGCCACAATTA	9873
rs747445193	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72912604	TTTGATGTGTCTTTG[C/T]CTGATTTTGGTATCA	9873
rs747462611	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73139063	GCCTTAGTCATAAAC[C/T]CTGAAGACAGGTATA	9873
rs747465670	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837758	CTTCCTTCCACGGAA[A/G]TGTCAGGGTAGTGGG	9873
rs747466755	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73095173	ACCTTGAGCGAGTTA[A/T]CTTTCCTGACTGTGC	9873
rs747476149	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72976062	CACAAACCAGCTGAG[C/T]TGATTTCTGTAGATT	9873
rs747483752	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72949950	GTTTGAGAAACCACC[-/A]AATGCTAATGTTCAC	9873
rs747486123	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72867836	TTCAGTGAAAATCAA[C/G]TTGTCATATCCAAGA	9873
rs747497341	snp	G/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839206	AAATGAAACATTTCA[G/T]TGTGTCTTGGGTAGA	9873
rs747506216	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72872656	CCAAATAACATTCTA[C/T]TGTATGGATATACAT	9873
rs747510209	snp	A/T	7.97099e-05	0.00631257	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841588	GAAGGAGAGATCTGC[A/T]GCAAAGGGAAGCGAG	9873
rs747521904	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73065033	TCATCCTGATACCAA[A/G]GCCTGACAGAGACAC	9873
rs747530320	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72921459	CGCTCCTTTTCCCTT[C/G]GTGCTCTTTTAGTAC	9873
rs747538666	snp	C/T	1.64963e-05	0.00287192	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842609	AATTCAACTGTCTCC[C/T]CTCTCAGGTACCTGA	9873
rs747553851	in-del	-/A	2.4551e-05	0.00350356	frameshift-variant, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838840	CTGCTGGCCTTCGGT[-/A]GATTCTGTGTAGGTG	9873
rs747555740	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72961292	GCTGGAGTGGGATCA[C/T]AGCTCACTATAGCCT	9873
rs747555867	snp	C/T	1.96845e-05	0.00313717	intron-variant	FCHSD2	GRCh38.p7	11:72889964	CAATACAAGAGAGAA[C/T]AGAGATAAAAATATT	9873
rs747567451	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72873959	TACTACCGTGCCACT[C/T]TAACCAATCAAATAT	9873
rs747578526	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73050413	CAGACATATATGTAC[A/C]TTTATAAACCATATA	9873
rs747581257	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72960945	CATACCTCTCACTTA[A/C]TATGTTTTCCTACTT	9873
rs747603871	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72859553	TATGATAGATATGTA[G/T]GTATAGGGAAAAACA	9873
rs747605545	in-del	-/AC			intron-variant	FCHSD2	GRCh38.p7	11:72925387	AAATTCCAGCTGGGT[-/AC]AGTGACTTGTGCCTA	9873
rs747616519	in-del	-/AGAGTATAATAAAAAAAAAAAAAAA			intron-variant	FCHSD2	GRCh38.p7	11:73049675	TGTACCCTAAAACTT[-/AGAGTATAATAAAAAAAAAAAAAAA]AAGAAAAAGGGGGAA	9873
rs747631217	in-del	-/CACACACAAACACACAC			intron-variant	FCHSD2	GRCh38.p7	11:72999880	AGACACACACACACA[-/CACACACAAACACACAC]ACACACACACTTTCT	9873
rs747637868	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73014507	TCTCAAGACACCTTC[A/C]ATGATATCAGTAGGC	9873
rs747655994	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72958595	ACGGAACAAAATCTA[A/T]TAAGTGAGTATTTCA	9873
rs747659581	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73046208	TCTTGCCCAGGCTAC[A/G]ATCGAATTCCTGTGC	9873
rs747660564	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73080875	CTTGAACCCAGGAGG[C/T]GGAAGTTGCAGTGAG	9873
rs747666159	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73134939	AACCTCCACCTCCCA[A/G]GTTCAAGTGATTCTC	9873
rs747681384	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72956285	AACTAAGAAAAGTAG[A/C]AGAAATGATGAAAAT	9873
rs747688258	in-del	-/ATA			intron-variant	FCHSD2	GRCh38.p7	11:73082630	AATCTCTCATTATTT[-/ATA]ATGAGAATAAAAACA	9873
rs747697773	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72847273	AAAGTGTTGGGATTA[C/T]AGGCATGAGCCATTG	9873
rs747704903	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72940031	GTGTTTTATGCGGCA[C/G]TGTTACAGCCTGTAT	9873
rs747725923	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72956443	CTATTTGTCTCAATC[C/T]GTTGAGGCTGATACA	9873
rs747730534	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73127043	TCTGTCTCAAAAGCA[A/G]ACAACAAAAAGAGTC	9873
rs747748872	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72986130	ATGCAGCCCAACTAC[G/T]TCCCCATTGTTAAAA	9873
rs747774745	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73038731	GCAAGGGTTGAAAAA[A/G]TAATTAGGCATGCTC	9873
rs747796955	snp	C/G	1.70362e-05	0.00291853	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843141	AAGAGTGCCTTGTTT[C/G]AGTCTTTACCACTGG	9873
rs747802828	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72882035	CTGTAGTCCCGGCTA[C/G]TTGGGAGGCTGAGGC	9873
rs747806521	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73010858	CTGGTAGTGGCAGCA[A/G]TGAGCTGGGTGGGTG	9873
rs747810192	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73129082	TTCACCATGTTAGCC[A/G]GGATGGTCTCGATCT	9873
rs747886740	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72926722	ACACAGGACAAGAAC[C/T]TGGGCAAAGGCACCA	9873
rs747891045	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73070964	AAGTTGCAAACTGGC[A/G]TCCTTCAGATGGGAA	9873
rs747893694	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73012870	TCTGCCAAATCATTT[C/G]CAAGTCCTCTGGCTT	9873
rs747899089	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72882180	GGGCATGGTGGCTCA[-/T]GCCTGTAATCCCAGC	9873
rs747924316	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73123053	TAATTTTAAAAGATA[C/T]ATAGGTGAAGGATAA	9873
rs747932275	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73104980	TATCAACAGACCAAG[C/T]CACAGAGGCTGTCAT	9873
rs747933553	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72966302	GTAGCTGGGATTACA[A/G]GTGCCCGCCACCACA	9873
rs747943617	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73023793	ATAAACAAACTGTGG[A/T]ACATAATTATAATGG	9873
rs747949146	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73138632	TTTTTTTTTTGAGAC[A/T]GGGTCTCACTCTGTT	9873
rs747957375	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73021631	TAATACCTGGGTAAC[A/G]AAATAATCTGTACAA	9873
rs747974370	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73108070	TCTCCACATCCTTGC[C/T]GGTGTTTGTTACTGT	9873
rs747975143	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72864373	TGAGACTAGCCTGGG[A/C]AACATGGTGAAAAAT	9873
rs747983595	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73071888	GTGCTTAGAACAGTG[C/G]CTGACACATGATCTT	9873
rs747986422	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72967671	TGGGGGATAACAGAA[A/G]TGTTCTGGAATGAGA	9873
rs748000242	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72878036	AAATAAAATATTAGA[C/T]AATATGATTAGGAAT	9873
rs748017056	snp	C/T	0.000131802	0.00811688	missense, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842763	TCTTTGTTCAAGATA[C/T]GGATTATTGCTCCCT	9873
rs748024059	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72889155	GAGATGGGGTTTCAC[C/T]GTAACACATGTTAGC	9873
rs748027354	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73048020	TCTATATTGTTTCTT[A/T]AAGTAGTACATACTG	9873
rs748040988	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72912416	TCATATAGTTTTTGC[C/T]CTTCACACAGAGTGA	9873
rs748068558	snp	C/T	1.68315e-05	0.00290094	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73015849	TTACTCCAGGCCAAT[C/T]TCTCTTCAGGTATTG	9873
rs748090882	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73030955	TTTTTTATCCTTTGA[C/T]CTAAGAAACTGTAGT	9873
rs748109834	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72921578	TCTCAAAGGCAATGC[A/G]CATGGCAATGGGCCA	9873
rs748116610	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73100952	TCAGAGCTCTCCTCA[C/T]ACAGACCCTTGTTTT	9873
rs748118469	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72940641	CCAGCCTGATAAAGC[A/G]CGCCGACCAGGCTGC	9873
rs748120938	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73136383	TGAGTAACATGGTAA[G/T]ACCCCATGTCTACAA	9873
rs748122196	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72924863	GACACTGCTGGTGTT[A/G]AGTCTGAATAAATTT	9873
rs748124902	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72908547	TCACCAGCATCTGTG[C/T]TACTGCCTATCTTTT	9873
rs748127248	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72999206	TGACAGGTATACCCA[A/G]TATGTACTGAATATT	9873
rs748134526	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72922257	GCTTAGGTGTAGGAG[-/T]TAAGTGAAATAATAA	9873
rs748149969	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72844798	AAATAAGGCAAAAAA[A/G]GGGTCATTTTCAAGA	9873
rs748153726	in-del	-/CTT			intron-variant	FCHSD2	GRCh38.p7	11:73012245	TTCTAAAATAGACTC[-/CTT]AAGTGTGTGGGCGGG	9873
rs748156748	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73017396	TACACGTAACTAAAA[A/T]GAACACAATGCTGAA	9873
rs748157496	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72993799	GCATTTGGAGATATA[C/T]CTAATGTTAAATGAC	9873
rs748158131	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72937894	CACCATGGGAAATAC[A/C]GAACATAAGATCAAA	9873
rs748186428	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73033469	GTAATCTCTAAGGTC[A/T]CCGCTTATAAACATA	9873
rs748188568	snp	C/G	4.70267e-05	0.00484883	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841569	GGAGGCGTGTGGCTT[C/G]GGGGAAGGAGAGATC	9873
rs748212723	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73133653	ATTGAAAAATTAGCT[A/G]GGTACGGTGGCGGGC	9873
rs748231538	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73088200	TCATACCATATTTTT[-/G]TTGTATCTTTCCTAC	9873
rs748233824	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72911695	TTATTATTATTATAC[-/T]TTTAAGTTTTAGGGT	9873
rs748242433	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72907031	TATGGCCATTTGTTT[C/G]CGTCCTCTTTTATTT	9873
rs748269627	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73003250	CTTTCATTTCCTCAA[C/G]TGGCAAATGGAGAAA	9873
rs748278333	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73031133	GAAAGAAGACGACTA[C/T]TATTTGATCTGTTAT	9873
rs748286462	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73066676	AAAAGTAGGCAAAGG[A/G]TATGAACAGACAGTT	9873
rs748286547	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73040711	TCATCTCAAACATTT[A/G]TCATTTCTTCATGTT	9873
rs748302390	snp	C/T	9.55795e-05	0.00691235	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140137	CTTTCACCTAAAATA[C/T]ACCATATATTTATGA	9873
rs748303731	snp	A/C	1.66957e-05	0.00288922	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842584	GAGCAATTTTCTTTA[A/C]ACATCTTTTAATTCA	9873
rs748305830	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72899939	TGTCATTAATTTACC[A/G]TATGACTCTGGACAA	9873
rs748313207	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73119195	TAGTCCCAGCTACTC[A/G]GGAGACTGAAGAGGG	9873
rs748317204	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72922431	AATATTAAAAAAAGA[A/G]AAGTGACTCAGAGAT	9873
rs748320406	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73132224	GAAACACGATAACTT[C/T]CTTTTGTACCTTGAA	9873
rs748341902	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72853875	CCTAAAACTGACCAT[C/G]AACAACAAATAATCC	9873
rs748352981	snp	G/T	1.97556e-05	0.00314284	intron-variant	FCHSD2	GRCh38.p7	11:72902676	TTAGGTCTTTAATGA[G/T]GTTAAAATGTCCAAT	9873
rs748362949	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72968246	ACTTTCTGAACAAAT[-/G]GAAAATAATTACAGA	9873
rs748389618	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73030102	GAATGCCATTAGTTT[G/T]AAAATATTTTTGCCT	9873
rs748389860	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73092366	GCTGATCTCAAACTC[A/C]TGGCTTCCAGTGATT	9873
rs748396336	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72974983	AAGAGCCACAACTCA[A/G]AATAAAAAAGATGAG	9873
rs748404241	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72948446	CATGTAGACAAATAT[A/C]ATAATAGATATTTAT	9873
rs748445392	snp	C/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839342	GCTTTATTCTGTAGG[C/T]AAAAGAGGAGTTTTT	9873
rs748452986	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73069920	AAAACAATAACTAAA[C/T]ATGTAAAAAAACAGA	9873
rs748453353	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73043088	GAACTTCTGCCACAA[C/T]GCTGAATAGGAGTGG	9873
rs748456874	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72950465	TTTTATATAGTTTTA[A/G]CTCTTAAGTCTTTGA	9873
rs748459634	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73106756	GTATCACAATTGCTT[A/C]AAGTATTCAGTACAG	9873
rs748467138	in-del	-/TTTAT			intron-variant	FCHSD2	GRCh38.p7	11:72948514	AGACAAAGAATATAG[-/TTTAT]TTTAAAGCATTTGAT	9873
rs748471116	in-del	-/TATTTATA			intron-variant	FCHSD2	GRCh38.p7	11:72903199	ATTTATTTATTTATT[-/TATTTATA]TATTTATATATTTAT	9873
rs748481080	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73006327	GTACAAAACTAAATT[A/C]TTGATTTCCCTAAAA	9873
rs748481456	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73075584	ATGGTGGGAGGCCAA[C/G]GAGGACGGATCACTT	9873
rs748484057	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72871242	ACTAGTCCTCCAAAC[G/T]CTAAAAACCAAGGCT	9873
rs748484166	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838174	ACGAAGGACACTGTT[A/G]TTTTAAGTCTGTTAG	9873
rs748484486	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72894564	ATCTTATTCTTTATG[A/G]AGTATATTAATATAT	9873
rs748489534	snp	C/T			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140560	CCAATGACCAATATT[C/T]ACACAATCATGATAA	9873
rs748528598	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72932555	TTTTTTGCCTCTGAG[C/T]TTTCACACAGGCTTT	9873
rs748530013	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73099731	TGGTTGGGGCTGTCA[A/G]GCCGGACCAAAAAGG	9873
rs748539414	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72880967	GCTTCTGGACATTGG[A/T]CAAGGGAGATTTTTA	9873
rs748549568	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73037500	CTCATAATTATGCCC[A/C]AAATTATTTTTTGCC	9873
rs748572936	snp	G/T	1.65326e-05	0.00287507	intron-variant	FCHSD2	GRCh38.p7	11:72984244	AAAATAAAATAATCA[G/T]TGCAAACTGATATTG	9873
rs748577324	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73127900	CAAGAGTTTGAGACC[A/G]GCCTGGCCAACATAG	9873
rs748581735	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72885342	CTATATTCAACATTT[G/T]TGATAAGAAAACTAT	9873
rs748587201	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72861183	AGAGAGGAGACATGA[A/C]CAATATCAGGAATGA	9873
rs748617827	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73018743	CAAATTTTTTAATAA[C/T]TGTATCAGATTTCTG	9873
rs748626464	snp	C/T	3.80069e-05	0.00435913	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72988974	CATACTTTGCCTCGA[C/T]GTCAGCTTTCTCTCG	9873
rs748628419	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73068173	GATGAGATTTGGGTG[C/G]GGGCACAGGCAAACC	9873
rs748651242	in-del	-/AG			intron-variant	FCHSD2	GRCh38.p7	11:73122558	GCATGGCTAAGGAAT[-/AG]AGACTTAAATTTCCT	9873
rs748665720	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73053574	GTAGTATACAAATAC[A/G]TTATCTCTTGTGAGT	9873
rs748666776	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72908489	GTTGTACTAATTTAC[A/C]TTCCCAGCAACAGTA	9873
rs748678642	snp	A/G			missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841514	CTGGGCTGGGGTAGG[A/G]GCTGCTGGGAGGCTG	9873
rs748685313	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73139380	TCTTTGTTGAACTGT[C/T]AGTCTGTATTACAAG	9873
rs748686088	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72960535	ACTGATAATGGATTA[C/T]GGCACTTGAGCCTAG	9873
rs748700554	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72931159	GGAGTGTAGTGGTGC[A/G]ATCAGGCTCACTGCA	9873
rs748704300	in-del	-/TG			intron-variant	FCHSD2	GRCh38.p7	11:72873531	CCCCATTCTGTGGGC[-/TG]TCTTTCATTTTCTTG	9873
rs748707251	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73036472	TAATTTCATTAGTCA[C/G]TTTGAGCTTTAGTTT	9873
rs748710085	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73005006	CTCCTATTACTTGCA[C/T]GAACTACCTGTGCTC	9873
rs748724466	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72952471	CTGGGATTACAGGCA[A/T]GTGTCACCACGCCCA	9873
rs748755228	snp	C/G	1.85197e-05	0.00304295	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841002	TTTACTTGAGTTGTT[C/G]AGCAATAATGCTGAT	9873
rs748757363	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73049873	GCACAAAAGGACCAT[A/T]AAAAAAAAATTGTTT	9873
rs748769706	in-del	-/TAAAGAGAAAATAAAA	7.15999e-05	0.00598288	splice-acceptor-variant	FCHSD2	GRCh38.p7	11:72902640	TAGTCCCGGACCACC[-/TAAAGAGAAAATAAAA]TATCTTTAGGTCTTT	9873
rs748785977	in-del	-/AGGAAACTTATCAGTAACAAGAATTTCATTGTCCCAAGAAGAAAAT			intron-variant	FCHSD2	GRCh38.p7	11:73070085	TGGCAAAAGTAAAAA[lengthTooLong]ATAGGGTAAACAAAG	9873
rs748809019	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73047863	GGTGAGCTAATGACT[C/T]TGTTATCTCATTTAA	9873
rs748814318	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73025007	CAGAAGTTGGCAAGG[-/T]CGTGGAGAAAAAGAA	9873
rs748824328	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73033545	GGAGGAATTATAGGG[C/T]GCTACACAAGACATC	9873
rs748876562	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73137816	AGCAGGGGGAAGAAA[C/G]AGGAAGGATGCATGG	9873
rs748882724	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73014679	GCTTCAATACTAAGT[A/T]CTCAATTACCCTGGA	9873
rs748882925	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72871027	GGCTGGCAGAAATAG[C/T]AGAGATTGAGAATAA	9873
rs748902180	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73132092	TGCTGATACCCATCC[A/C]GCAAGTTCTATGCAT	9873
rs748903589	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73028453	TATCAAATGCCTGTA[C/G]CCCCATTGTATCTTG	9873
rs748915265	snp	C/T	3.32298e-05	0.004076	intron-variant	FCHSD2	GRCh38.p7	11:72887609	AATAATGATGACTGT[C/T]TTTTACTTTTCATCT	9873
rs748918413	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72903894	TACTGCTTCCCTCCC[C/G]CTCACTCCACCAACC	9873
rs748926730	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73115765	TTGAGGCAAAATTTC[C/T]TCTTCTTCCAGATAC	9873
rs748931317	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72978635	GCGATTTCCCTGATG[C/G]TGTTCTCATGATTGT	9873
rs748938354	in-del	-/AAG	1.75007e-05	0.00295805	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840976	TAAGGGAGAAAACCA[-/AAG]AAGCTCATTTTACTT	9873
rs748938816	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73015373	TACATTAGAAAGTTT[-/C]CCCCCTAGTCTCACA	9873
rs748950790	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72919164	CTTCCCTTTAGGTTG[A/C]TTTCAGCAGCATAGC	9873
rs748966822	snp	C/T	0.000164788	0.00907562	synonymous-codon, utr-variant-3-prime, nc-transcript-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842792	CTCAGGAAAAGATAA[C/T]TCATCATCTGTCTGG	9873
rs748974353	snp	A/G	3.29576e-05	0.00405928	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843431	ACAAGAAAGGGCGAT[A/G]TGAGCAAAGGAATAT	9873
rs748986412	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72879540	TTTAAAGAAAAACAT[A/G]AAGATAAATAGGAAT	9873
rs748991921	in-del	-/TTGT			intron-variant	FCHSD2	GRCh38.p7	11:73098313	TCTTTGATCTACTCG[-/TTGT]TTAAGAATATGTTTA	9873
rs748999134	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72858076	ATGTTTGGTGCATAG[A/G]AGGTACTTAATAAAG	9873
rs749003948	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72958746	GTCACTTAAAAGTAA[C/T]CAGATTTAAGAAAAA	9873
rs749005398	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72998155	TCTAACAGCCAAAAA[A/G]TCATAAATGAGAGTT	9873
rs749030704	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73048158	CAAACTGCAAAAAGT[A/G]AAAATCTGACCCAAA	9873
rs749038308	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72911889	TTTGGTTAATTCCTA[C/T]GTATTTTAATGTATT	9873
rs749044301	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72913660	TTTCTGTGGTATTGG[C/T]TGTAATGTCTCCTTT	9873
rs749056876	snp	C/T	2.26078e-05	0.00336205	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72921872	ATGTGTTCTGCACAG[C/T]TTGGCATGTTTCTAG	9873
rs749069973	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72952482	GGCATGTGTCACCAC[A/G]CCCAGCTAATTTTTA	9873
rs749073358	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73109911	TATCATGAAGGAATA[C/T]TAAATTTTATTAAAT	9873
rs749080820	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73111764	GTGTATCTGTTATAT[G/T]ATTTTTGATTTGAGG	9873
rs749089733	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73111720	ATTTTCTCTGGTGGG[A/G]TGTTTTAATTTCTTG	9873
rs749124128	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72953586	ATCAAGAGTCTACTA[C/T]TTGTCAGACATTATT	9873
rs749124405	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72846732	TCTCCAAATTTCCTG[C/T]ATTTCTTTTAAAACA	9873
rs749126909	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72852718	ATTGCAGCACTATTT[A/G]TACTAGCGAAGACAT	9873
rs749138038	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72866415	GCTGGGATTATGGGC[A/G]TCTGCCACCATGCCT	9873
rs749149007	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73072537	TTTCTAAACACTGTT[A/G]TAAGATAAGGAAAAA	9873
rs749162724	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73034810	ACCAGAACTTCGAAG[C/G]AGCAAAAGAAAATAA	9873
rs749162889	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73021728	ACTTAAAAAAAAAGC[C/T]CATTCATGACAGAAT	9873
rs749169818	snp	C/T			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143489	AGCAGTGCACCCCAC[C/T]ACCACACATGAACCT	9873
rs749180350	in-del	-/CT			intron-variant	FCHSD2	GRCh38.p7	11:73047831	AATATTTGCTAATGA[-/CT]GTATATACAAATGAT	9873
rs749180515	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72878370	TAAAAAAAGTTATCC[A/C]TAGCTCTAACAACAA	9873
rs749185922	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73081509	GTATTAAAAATTTTT[A/T]AAGCATATCATAGAC	9873
rs749195782	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72964921	CAGCCTCCCGAGTAG[C/T]GGGGACTACAGGCGC	9873
rs749221039	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72928479	CTCTTGGCCTAGAAT[A/G]TCCTTCCCCCCTTCT	9873
rs749225080	in-del	-/AG			intron-variant	FCHSD2	GRCh38.p7	11:72882724	AGTGCCTAAATAAAT[-/AG]AGAGACACATCATGT	9873
rs749233608	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72850648	GTGAGCCACCGTGCC[C/T]GGCCAGGACAGAGAT	9873
rs749239138	snp	A/C	6.78288e-05	0.00582321	intron-variant	FCHSD2	GRCh38.p7	11:73000984	GAACAGAAATAAAAA[A/C]AATACCCTTTTTAGT	9873
rs749241529	snp	C/T	1.67203e-05	0.00289134	intron-variant	FCHSD2	GRCh38.p7	11:72849705	ATACAGTCATGTGTA[C/T]CTTCAGAGTTAATCA	9873
rs749265906	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73124108	CGTTCACGTCCTTTG[C/T]AGGGACATGGATGAA	9873
rs749273168	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72879383	TCACTATGTCTAGAT[G/T]CAGTAAAAACTTAGT	9873
rs749285691	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73022571	AGTCCATAATACTAA[C/T]GAAAGAAAGAAAAGA	9873
rs749292142	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73057057	CACTGCACTCTAGCC[C/T]GGGCGACAGAGCAAG	9873
rs749310257	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73068989	CACTGCACTCTAGCC[G/T]GATGACAGAGCAAAA	9873
rs749320299	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72908605	TATAATATCTTACTG[C/T]AGTTTTGATTTGCAT	9873
rs749326905	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72939396	GGTTTTTAAATTATT[A/C]AACAAAAATTAAGTT	9873
rs749327485	snp	A/C/G	0.000165817	0.00910418	intron-variant	FCHSD2	GRCh38.p7	11:72867861	CCAAGAAAAGAAATC[A/C/G]TACCGAGTGTAAAGT	9873
rs749336301	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72894769	AAAACTCACTTGAGC[C/T]AAAATGTGATTTGAA	9873
rs749348800	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73120445	CAGAAACATATGAAG[A/T]TAGGCCAGGAGCAGT	9873
rs749376981	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72911002	TTTTTAACTTGATGT[C/G]ATCCCACTTGTCCAT	9873
rs749379374	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73058918	CTTTTTTGGATCACT[G/T]ACCAACCAGAAATAT	9873
rs749390574	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73091700	TGTGGTCTTTTCCAC[G/T]TGGAATTTCCTCCCG	9873
rs749405496	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73053961	ATAATTCACTTTTAT[C/T]GTATTTTACAAAAAT	9873
rs749406715	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73139750	CAATTCCGTGGAAAG[A/G]TTATTTAAACAAGAA	9873
rs749417568	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72948877	TCACCACGTTAGCTA[A/G]GATGGTCTGGATCTC	9873
rs749420617	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72965709	CACTCTTTCCCATTC[G/T]ATGTACACCCCTCAC	9873
rs749443033	snp	C/T			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140796	GGAGAACAGCAAATG[C/T]CTGCTGGCCAGAGAG	9873
rs749466926	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72995897	ATTTATCCTAAGAAA[A/C]AAATTTAAAAAGTTA	9873
rs749469386	snp	A/G			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840700	TAGATTAAATGTCCC[A/G]AGATGAGTTGATTTC	9873
rs749471907	snp	C/T	2.43579e-05	0.00348975	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72867929	TCATTTTCCAGTTCT[C/T]CCATTACTTGGTTCA	9873
rs749472013	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72978259	GCACATGTATACATA[C/T]GTAACAAACCTGCAC	9873
rs749472014	snp	C/T	0.000101942	0.00713867	intron-variant	FCHSD2	GRCh38.p7	11:73140022	TTGAACTATTTACTA[C/T]AGCCTTACCTCATAT	9873
rs749481772	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72976695	GTATGGTACTGGCAT[A/G]AAAATAGACTCACAG	9873
rs749487064	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72908870	TGTTGCCCAGGCTGG[C/T]CTCTAACTCCTGGGC	9873
rs749487380	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72923076	CTGGCTTCTGTTGCC[C/T]AGCATAATATTTTCA	9873
rs749504440	in-del	-/TTATC			intron-variant	FCHSD2	GRCh38.p7	11:72918239	CTGATTTTTGTGTTT[-/TTATC]TTATATGTTGCTAAA	9873
rs749518810	snp	A/G	0.000156928	0.00885659	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841560	TGGAGGCAGGGAGGC[A/G]TGTGGCTTGGGGGAA	9873
rs749521135	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73063544	GTATTCAGGAGACCC[A/T]TCTCATGTGCAAAGA	9873
rs749521440	snp	C/T	2.07303e-05	0.00321943	synonymous-codon, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841494	GTACAGGGAGCTCCT[C/T]TTATCTGGGCTGGGG	9873
rs749530121	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73134730	CTTTGGTGAAACTCA[C/T]GTTAACGGTTTGAAA	9873
rs749539444	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73019080	ATGAGGAAAAGATCA[A/T]CTGGTATTTTCTCAA	9873
rs749556858	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73028546	ATGAGACTTTGGCCT[C/T]GGACTTTTGGGATAA	9873
rs749567911	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73129392	TTCGTCCATACTTAC[A/T]GCCGCCCCCGCATTG	9873
rs749593246	snp	A/G	1.90391e-05	0.00308532	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843115	CAGTTTAGGTCAAAC[A/G]TGACCAAATAAAGAG	9873
rs749606299	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72919628	AGAAATTGTTAAGTG[C/T]GTGTAAAATATTAGC	9873
rs749607211	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73094190	CACTCCAGCCTGGGC[C/T]ACAGAGCAAGACTCT	9873
rs749633750	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73027438	AGCAAAGCATTCAAA[A/C]TGTAACCTGGCTTTT	9873
rs749638461	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73041103	CCATTGTGTATATAA[A/T]CCATATTTTCTTTAT	9873
rs749644671	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72987818	CAAGTTTCTAAAAAC[A/G]ACTATGACAGTATAT	9873
rs749657024	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73039077	ATAATAATTGCAGAA[A/T]CACTGTTTATTTTTA	9873
rs749666335	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72956923	ATCATGCACTTCTTC[A/G]TGTGATACATAGAGA	9873
rs749705988	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72973379	TCTCAAAAAAAAAAG[A/G]AAGAAAAGAAAAGAA	9873
rs749706606	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72844402	ATGGTTTGGATTTCT[C/T]ATGCTCCAACTTAAC	9873
rs749715322	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73088595	AACATATAATGTTTG[-/A]AAAAAAAAGTCCTTT	9873
rs749730627	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72850188	GTGCCTCAGTCTCCC[A/G]AATAGCTGGGATTAC	9873
rs749733650	snp	C/T	2.32275e-05	0.00340781	missense, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72984093	GCTGTATTACCTTCA[C/T]AATGTTAACTAAATC	9873
rs749738163	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72864016	TTATCTTACCCTTAT[C/G]TCCAACATCATTATT	9873

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