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

SEH1L

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs533458586	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12963862	GAATTACAGGCATGC[A/G]CCACCACGTCTGCCT	81929
rs533495668	snp	G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12962829	GTGACAAAACTTCTT[G/T]TCTGAAAATTCTAAC	81929
rs533573285	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12969595	TGGGAGGCCGAGGCA[C/T]GAGAATCGCTTGAAT	81929
rs533598606	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976104	TGGCTGAAACAGTAC[A/G]GATTCGGTATTTCAA	81929
rs533695098	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12950647	CTAGAAGATAAATTA[G/T]TGGATATTTTAAACA	81929
rs533944948	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955709	TAAAATATCACCACT[C/G]CCCTCTAGTTTTACC	81929
rs533947156	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949325	CTTTTTCACATTCGA[C/G]TTTGATACCAGTGAT	81929
rs533988784	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955159	ACTCTCCAACTATCA[A/G]CACTGGAAGTAGTCA	81929
rs534077541	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12972530	TGATCAGATGGGCTT[C/T]GCAGGTACTAGACAA	81929
rs534143913	snp	C/G	0.00438332	0.0466095	intron-variant	SEH1L	GRCh38.p7	18:12965263	GTGATCCGCCCACCT[C/G]GGCCTCCCAAACTGC	81929
rs534145877	snp	C/G	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12962164	AACTCGGGAGGCTGA[C/G]GTGGGAAGATCAGTT	81929
rs534178566	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12984395	TTATGAAGTCATTAC[A/G]TTATATTCTGAAGCT	81929
rs534185610	snp	G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12970984	TGTGACATTCTCAGG[G/T]GCATACTTGCAGTGT	81929
rs534218140	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12983809	GTAAGATGGGTGGTG[A/G]AAGCTTTATATTTTT	81929
rs534326620	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12976975	GCCAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	81929
rs534409034	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12964855	TGTTAGCCAGGCTGG[A/T]CTTGAACTCCTGACC	81929
rs534414303	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946903	CATTCCTGGCCAAAA[A/T]CCAAAGGGCAAGTCC	81929
rs534425732	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971548	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG	81929
rs534458934	in-del	-/A	0.00279162	0.0372561	intron-variant	SEH1L	GRCh38.p7	18:12958952	CAGCTACACCATTTT[-/A]ACATTCCTACCAGCA	81929
rs534595550	snp	C/T	0.105924	0.204309	intron-variant	SEH1L	GRCh38.p7	18:12980244	TCCCGGACGGGGCGG[C/T]TGGCCCCCCCACCTC	81929
rs534668940	snp	G/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12953888	CCAATAAATATACCA[G/T]TTTGCTTAACTAGTG	81929
rs534834940	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12959697	GTTTCCTTTGATGCA[C/T]GAAATTTTAAAATTT	81929
rs534918539	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12981344	GCACTTTGGGGGGCC[A/G]AGGCAGGCAGCTGGG	81929
rs534927747	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12976790	TAACATGGTGAAACC[C/T]TGTCTCTACTAAAAA	81929
rs535040991	snp	C/G	1.83538e-05	0.00302929	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948244	TAAGGTGCGCGCGGC[C/G]CTTGCGGGCGGGGCC	81929
rs535261506	snp	G/T	0.00478085	0.0486577	intron-variant	SEH1L	GRCh38.p7	18:12960573	CTCTTCTCAGGGGAG[G/T]AGTATGTCTGATTGC	81929
rs535419825	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974604	TTCTAAGTAGTATCA[A/C]CATTTAGTAGACAGG	81929
rs535458519	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12980957	GACGGGGTGGCTGCC[A/G]GGCGGAGATGCTCCT	81929
rs535478876	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12980835	GGCTGACCCCCCCAC[C/T]TCCCTTCCGGACGGG	81929
rs535543379	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948297	AGTGGGTGGGCGGCG[A/C]GGGGAACGGGGCTGT	81929
rs535551351	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12957307	GTGGCACATGCCTGT[A/T]ATCCCAGCTACTCAG	81929
rs535581396	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12953994	ATCTAATAAAACTTA[C/T]CTGCCTTAGTGTGCA	81929
rs535631756	in-del	-/G	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime	SEH1L	GRCh38.p7	18:12987645	ATCCAAGTAGGTTAT[-/G]TAATAAAATATATTT	81929
rs535670460	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976206	CTCGTGTTCCTGCCA[C/T]GAGACCCTCCCTTGT	81929
rs535706709	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12973858	TTAGTACACTGGTGA[C/T]AGCTCCCTCTTATGA	81929
rs535728469	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12982008	GGGACTACAGGCGCC[C/T]GCCACCATGCCTGGC	81929
rs535817814	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951540	GGACTATAGGCATGC[A/G]GCACCATGCCTGGCT	81929
rs535857495	snp	G/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12950982	GTGCACCACCATGCC[G/T]GGTTTCAATATTTTT	81929
rs535894151	in-del	-/ACTC	0.00478085	0.0486577	intron-variant	SEH1L	GRCh38.p7	18:12962499	TTGAGAGAGGGTCTT[-/ACTC]TGTCACCCAGGCTGG	81929
rs535933627	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954584	TGATCCTCCCACCTC[A/T]GCCTCCCAAGCAGCT	81929
rs535944498	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12975558	GAGCAAAGACAAGGG[C/T]GTGGGGTCGAGGCGG	81929
rs536018946	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12979073	AGTTACTTTTTTTTC[C/T]TTCTTTTTTTTTTTA	81929
rs536058831	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12978552	TACATTTTCAAAGAC[A/G]CTATTTTTGAATAAG	81929
rs536108211	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12966593	TTTTTGTGGATATGG[C/G]GTTTCGCCTTGTTGC	81929
rs536388665	snp	A/C	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12973369	CAGTGATGCAATCTC[A/C]GCTCACTGCAACCTC	81929
rs536503739	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985650	ATTTCTTTTGCTTTC[C/T]TAAAACAGCTTAAAA	81929
rs536561316	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12969517	ACATGGTGAAACCTC[A/G]TCTTTACTAAAGATA	81929
rs536652921	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12966266	CCCGTCTAATTTTAT[A/G]TTTTTAGTAGAGATG	81929
rs536738341	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952001	AAAATAACATTTATA[C/T]AGTAGTTCTTTTCCT	81929
rs536772425	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12957770	AATGGCATGATACTA[C/T]GTTAGAGCCAGTCAC	81929
rs536814452	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12953151	TTTGTGTCTGGCCAC[C/T]TTCCCTTTGCATGTT	81929
rs536814801	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946985	GCTTCCACTGTCTCC[C/T]ATCCTAACTTTACCA	81929
rs536826047	snp	G/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12974024	ATGCCTTAGCTGCAA[G/T]AGAGTGAGACAGCAA	81929
rs536849817	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12952477	ACCTCAGGTGATCCT[C/T]CCTCGGCCTCCCAAA	81929
rs536863824	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12959470	ACAGGTGTGAGCCAC[C/T]GTGGCCAGCCCCAGT	81929
rs536901340	snp	C/T	7.6536e-05	0.00618564	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986885	TTACCCCTCTGGATT[C/T]CCCACGGGCTGGATC	81929
rs536952257	snp	C/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947181	AGCAGCCCACTTCCC[C/T]GGCCGCTTCCTTCCC	81929
rs536963726	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946769	TTATGGTTGAAAAAG[A/G]TCAGGTCATTGCGCC	81929
rs537019530	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12959539	TTCAATAAGCATTTT[C/T]TTTGAGCATCATGCC	81929
rs537037602	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986349	GCTTTTGCAGAAAAA[A/T]AAGTGTTCAATGTTT	81929
rs537048682	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12967840	AATCGCTTGAACTTC[A/G]GAGATGAAGGTTGCA	81929
rs537275692	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12956356	CAAGGGTTAATAAAA[C/T]TCTTTAAATTTTATT	81929
rs537359972	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12980692	GCTGGCAGGGCGGGG[A/G]GCTGACACCCCCCAC	81929
rs537444642	snp	C/T	0.0142736	0.0832652	intron-variant	SEH1L	GRCh38.p7	18:12962371	AGAGCAAGACCCTGT[C/T]CCTAAGAAAAAAAAA	81929
rs537452629	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12970700	AAAATGCTGGGATTA[C/T]AGGCATGAGCCACCC	81929
rs537459448	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12958789	ACTTCGTGGCTATTG[C/T]GAATACTGCTACTAT	81929
rs537589753	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974520	CTTGATCTTGTGATC[C/T]GCCCACCTCAGCCTT	81929
rs537594904	snp	C/T	0.000103891	0.00720656	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948109	CTTCGGAGGCGCGGG[C/T]CCGACGGAAACCATG	81929
rs537702774	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12978202	AGGAGGAAACGTGGG[A/C]GGTTGTATTAATTTC	81929
rs537732009	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947506	ATGTGTCTGGGGGGA[A/G]ACACATCCAAACGTC	81929
rs537734235	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12959436	ATCCTCCACCTTGGC[C/T]CCCCAGAGTGCTGGG	81929
rs537811355	snp	A/T	9.82077e-05	0.00700673	intron-variant	SEH1L	GRCh38.p7	18:12963139	TGTATATAATTTAAA[A/T]TGTTATTATTTTTTT	81929
rs537867214	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985352	CCAGCGCCGTTTGAC[C/T]TCTCCCAAGATACAC	81929
rs538091398	snp	C/T	0.00597247	0.0543191	intron-variant	SEH1L	GRCh38.p7	18:12978551	TTACATTTTCAAAGA[C/T]GCTATTTTTGAATAA	81929
rs538131025	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12950454	AAAGTGAAAAAATTA[C/T]AGACTTATTGCTAAT	81929
rs538217853	snp	C/T	0.00318978	0.0398085	intron-variant	SEH1L	GRCh38.p7	18:12971590	AGTGAGCTGAGATTG[C/T]GCTATTGCACTCCAG	81929
rs538252103	snp	A/T	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12978003	CCAGCTATTTCTGTA[A/T]TTTTTGTAAAGATGG	81929
rs538394740	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971439	GAGAAAGTAGACCAG[C/T]CTGGCCAATATGGTG	81929
rs538405670	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12966144	GTCACCCAGGCTGGA[C/G]TGCAGTGGTGTGATC	81929
rs538440849	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12965254	CCTGACCTTGTGATC[C/T]GCCCACCTCGGCCTC	81929
rs538443382	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985500	CTTTCTGTTGAGACA[C/T]TGTCACCAAAACAAT	81929
rs538481530	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12984704	TTTTAGAATATTTAG[C/T]ATATGTTACATTCTT	81929
rs538894158	snp	A/C			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946450	AATTTTGCTGTGAAC[A/C]TGAAAGTGTTCTAAA	81929
rs539017238	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12965311	GCCACCTCGCCCAGT[C/T]CATTTCCTAATTCTT	81929
rs539046921	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12972527	AGGTGATCAGATGGG[C/T]TTCGCAGGTACTAGA	81929
rs539192386	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952100	AATCTGTAATTCTGT[A/G]GCATTCTAACATAAT	81929
rs539206934	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12958482	CTCAAAACTGTTCAT[C/T]ACTGCCAACATAAAC	81929
rs539224610	snp	A/C	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12954666	AGTGATGGCATTTTG[A/C]CATATTGCCCAGACT	81929
rs539336317	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12960920	AAGTTTTAGAGCCAG[A/G]GTGGAAATTTGTTAA	81929
rs539543185	snp	C/G	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12953665	CCAAGGTCCCCCCCC[C/G]TTTTAAGGTGAGGTT	81929
rs539578852	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949010	GCACGCCACCACCCC[C/T]GGCTAATCTTTTTTT	81929
rs539675483	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951451	GCTGGAGTGCAGTGG[C/T]GTGATGTCAGCTCAC	81929
rs539704761	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976703	GGGCGCAGTGGCTCA[C/T]GCCTGAATCCCAGCA	81929
rs539884815	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970865	TATCTTTTAAAAATA[C/T]GTTGAATGCTTGAAA	81929
rs539954005	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955035	AGCAAATAAATCTAA[C/T]GTTATTTATTTTATT	81929
rs540047542	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12977070	GCTGCTGCAGACCAC[A/G]CAGTAGAAGCAAGGA	81929
rs540100263	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12983556	ATTTTTCATTCAAAC[A/T]AATAAGGCCATTTTG	81929
rs540207920	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948497	CGCCGGGCCCTCTCC[C/T]AGGCCGCGCTGCCGG	81929
rs540221851	snp	A/G	0.00279162	0.0372561	intron-variant	SEH1L	GRCh38.p7	18:12954282	GGTGAAATTCTTTAA[A/G]ACCTTTGTATCCCTT	81929
rs540257006	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12960874	GAAAGAATTCCACCT[A/C]GGGGCATAAGGCAGA	81929
rs540281198	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12969035	GACCAACATGGAGAA[A/G]ACCCTTCTCTACTAA	81929
rs540291109	snp	A/G	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12960098	GCCTTGAGCAACCAG[A/G]TGTCTGGTTGTTAGC	81929
rs540411257	snp	G/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12956017	AATTCTTTTTTTTTT[G/T]TAACTTTAAACTCTT	81929
rs540413322	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949715	ACCTCGGCCTCCCAA[A/G]GTGCTAGGATTACGG	81929
rs540433874	snp	G/T	0.119978	0.213528	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949026	GGCTAATCTTTTTTT[G/T]TTTTTGTATTTTTTA	81929
rs540663655	snp	A/C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976760	ACGAGGTCAGAAGAT[A/C/T]GAGACCATCCTGGCT	81929
rs540665118	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12973510	TCACCATGTTGGCCA[C/G]GCTTGTCTTGAACTC	81929
rs540688111	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12965359	GCAAGATTTATAATA[A/T]TTACATTCTGTAAAC	81929
rs540720372	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947735	GGGACGAGGATTGAC[A/G]AGCCGGGAACAGGGC	81929
rs540751016	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12982346	ACATTGGCCCAGCTC[A/G]AGGGCCAAGGTGTGG	81929
rs540813553	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952253	TTTTTTTTTTTGAGA[C/T]GGAGAGTCTTGCTCT	81929
rs540878226	in-del	-/A	0.0524604	0.153226	intron-variant	SEH1L	GRCh38.p7	18:12962378	GACCCTGTCCCTAAG[-/A]AAAAAAAAAAAATAA	81929
rs540882080	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12962618	GGCCACAGGCGTGCA[C/G]CACCACACCTGGCTT	81929
rs540929865	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12966386	CGTGAGCCACCGCAC[C/G]CAGCCACCATTTATT	81929
rs541053828	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12972863	TTAAAGTAAATTTCA[A/T]CCTGAGCTGAGCAGA	81929
rs541059564	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12979323	AGCACATCTTGCACC[A/G]CCCTTAATCCATTCA	81929
rs541071324	snp	C/T	0	0	downstream-variant-500B	SEH1L	GRCh38.p7	18:12987706	ACAGAATGTATTTTA[C/T]TTAAGATAATTGCCA	81929
rs541075002	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947098	CTTGATCTGAGCCAG[A/G]CCTCTTCCCAGGGGC	81929
rs541100188	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986435	TCATGTACGCACTAA[A/C]AAAAATGTGTGCTTG	81929
rs541173356	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12952820	GGCGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	81929
rs541279262	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12957318	CTGTAATCCCAGCTA[C/G]TCAGGAGGCTGAGGC	81929
rs541294749	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12981109	ACTTCTCAGACAGGG[C/T]GGCCGGGCAGAGATG	81929
rs541304807	snp	A/G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12975255	CTTCGGCCTCCCAAA[A/G/T]TGTTGGGATTACAGG	81929
rs541333429	snp	C/T	0.00676609	0.0577691	intron-variant	SEH1L	GRCh38.p7	18:12980687	GGGTGGCTGGCAGGG[C/T]GGGGGGCTGACACCC	81929
rs541347691	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12972569	AGTCTAATAGTCAGA[A/T]CTTAGGCAGGGCCAG	81929
rs541436367	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12967635	CATGAAAGCCTGGGC[C/T]GGGCACAGTGGCTCA	81929
rs541609431	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12975411	CTTACAGCGCCTAGG[A/T]TATGGATGAGGATGG	81929
rs541627273	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952927	GCTGGGATTACAGGC[A/G]CATGCCACCACACCC	81929
rs541810005	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12975061	GCAATGGTGTGATCT[C/T]GGCTCACCGTAACCT	81929
rs541822843	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12966523	ACCACACACAGCCTC[C/T]CAAGTAACTGGGACT	81929
rs541864557	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974117	GTGGGGGTGTGTGCT[A/G]TTGACTTGGGAAGTA	81929
rs541897463	in-del	-/CTC	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12960563	TGTTTTACAGCTCTT[-/CTC]AGGGGAGGAGTATGT	81929
rs541901020	snp	G/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12980389	ACCCCCCCACCTCCC[G/T]CCCGGACGGGGCGGC	81929
rs542010786	snp	G/T	0.00398564	0.0444627	intron-variant	SEH1L	GRCh38.p7	18:12959932	GGTTTATTCGATTTG[G/T]CTAAAGCAAGAAGAT	81929
rs542030987	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12969149	GGGAGGTAGAGGTTG[C/T]GGTGAGCTGAAATCA	81929
rs542093081	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12974472	TTTAGTAGAGATGGG[A/G]TTTCACCATTTTGGC	81929
rs542244305	snp	C/T	3.30819e-05	0.00406692	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984178	ATTCATTAAATGGAT[C/T]TTCTGCTGGCAGGTA	81929
rs542251648	snp	A/C	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12984771	GTCTGTTTCCATGTT[A/C]AAATTTTAAATATGT	81929
rs542363243	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12950402	TATTTATTTGTATAT[A/G]TTTTTAATTGAGCAA	81929
rs542430474	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971830	TGACCTATAGGGTGA[C/G]TAGAAGTTAGCCAGA	81929
rs542447211	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12945988	AGCACTAAAAAGAAA[C/T]GAACTCTCAAGACAA	81929
rs542783371	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12964823	TTTGTATTTTTAGTA[C/G]AGACGGGGTTTGTCC	81929
rs542793936	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12965354	TACTGGCAAGATTTA[C/T]AATATTTACATTCTG	81929
rs542820420	snp	G/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949456	CGTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTG	81929
rs543076168	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985733	GATTGTTTTGAGTGC[C/T]GATTTGTTTACTTTT	81929
rs543131332	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985818	ATTTAAAAAATATTA[C/G]TAAAGGAGTGAATTA	81929
rs543136962	snp	C/G	0.00597247	0.0543191	intron-variant	SEH1L	GRCh38.p7	18:12970100	GAACTAATTTTTTTT[C/G]TCAGTTACCACATTT	81929
rs543183887	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12957150	ATACTGTCCTCGGCC[A/G]GGTGCGGTGGCTCAC	81929
rs543193256	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12966369	AGTGTTGGGATTACA[A/G]GCGTGAGCCACCGCA	81929
rs543207331	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12983411	CCAGACCTTCCTTTC[C/T]TCAGTGTAATTTGAT	81929
rs543228124	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12973446	CTGGGATTACAAGTG[C/T]GTGCCACCACGCCTG	81929
rs543236709	snp	C/T	0.00716266	0.059414	intron-variant	SEH1L	GRCh38.p7	18:12979524	TTCCCCACCTTTCCC[C/T]GCTTTCTATTCCACA	81929
rs543255353	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946288	GAGTGAACCCTAATG[C/G]AAACTCTGAATTTTG	81929
rs543266850	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12972701	TTGGTGTCTGCAGAG[A/C]GGCTCAGTCTTCAAC	81929
rs543290416	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12957127	TTACTTTTGTTTTCT[C/T]AGGAAATATACTGTC	81929
rs543391574	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952145	AGAATATTCCTTTTG[C/T]CTTTACATATTTTAA	81929
rs543441206	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12978275	CACAGAAATGTATTC[A/G]CTCACAGTTCTGGAG	81929
rs543458279	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952208	AAAAAAAAAAAACAA[A/T]ACCTTTACTCAAGTA	81929
rs543725701	in-del	-/G	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12977500	GAGGCAGAGGCGGGT[-/G]GATCACCTGAGGTCA	81929
rs543807165	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946442	TTCTGCTCAATTTTG[C/T]TGTGAACCTGAAAGT	81929
rs543994294	snp	A/G	0.0182019	0.0936463	intron-variant	SEH1L	GRCh38.p7	18:12980997	GACGGGGTGGCTGCC[A/G]GGCGGAGGGGCTCCT	81929
rs544017451	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954303	TGTATCCCTTCTCCA[A/G]CCACCTCCCCTCCCA	81929
rs544142270	snp	C/T	0.00478085	0.0486577	intron-variant	SEH1L	GRCh38.p7	18:12982448	ACGTGTGTATATATA[C/T]ATGTGTGTGTATATA	81929
rs544192318	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949047	GTATTTTTTAGTAGA[G/T]ACAGAGTTTCACCAT	81929
rs544195752	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12954846	CATTTAAAGTGTACA[A/G]TTTAGTGATTTTAAG	81929
rs544297514	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12962805	TCTAATGCTTGCAGC[A/G]TGCTTTGTGTGACAA	81929
rs544328662	in-del	-/CCC			intron-variant	SEH1L	GRCh38.p7	18:12969226	GCCCCCCCCCCCCCC[-/CCC]ACCTCACCAAAAAGA	81929
rs544332468	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12961754	TCAGTGCAGCCTCCG[C/G]CGACCACACTCAAGC	81929
rs544405172	snp	C/G	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12950555	ATACGTATATGTCTT[C/G]TCAGAAATAGTGTTG	81929
rs544420111	snp	G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12982983	GCTCTACAAACTCAG[G/T]CTAGGACTGTAGTGG	81929
rs544574763	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12963748	GACAGAGTATTGCTC[A/G]TTTGCCCAGGCTGGA	81929
rs544647932	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12950278	TGAGCTCAAGTGATC[C/T]TCTCACCTCAGCCTC	81929
rs544669245	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970491	AGTGGCACGATCATA[A/G]CTCACTGCAGCCTCC	81929
rs544829923	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12967930	AAAGAGAAAAAAAAG[-/A]AAAAAAAAAAGAAAG	81929
rs544875606	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12978178	TTCGAGCTAAATGTA[C/T]ATTATTAAAGGAGGA	81929
rs544910495	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12983144	TAAGTGCCAGGCTGA[A/G]TGAGAAGGTCTGGTC	81929
rs544964105	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12964321	TTAATTCTGGTAGTC[A/C]CTAGTATATTTTTAA	81929
rs544995804	snp	G/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949675	AGCCAGGATGGTCTC[G/T]ATCTCCTGACCTCGT	81929
rs545133475	snp	A/G	0.00438332	0.0466095	intron-variant	SEH1L	GRCh38.p7	18:12971705	GTGAAACAAAAAATA[A/G]TAGTAAAAAAGGGTG	81929
rs545282192	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951634	GACCTCAGGTGATCC[A/G]TTTGCCTTGGCCTCC	81929
rs545295813	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12971862	AAAGAGGGCAGAAGC[A/C]CTCCTGGTGGAGAAA	81929
rs545392935	snp	A/C			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985534	TTGAAATGTTCCTGA[A/C]ACTAATTTGGGTTTA	81929
rs545437844	snp	C/T	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12964459	AACTGATAGAAAAGA[C/T]GAATAGAGCACATTT	81929
rs545474702	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12963878	CCACCACGTCTGCCT[A/G]ATTTTTGCATTTTTA	81929
rs545799521	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12960024	ACTAGATCTAGTAAG[C/G]GAGGGGGAGTTTCAC	81929
rs545949202	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948399	TCCCCGCCCGCGTAT[C/T]GTGGGGTCACGGCGG	81929
rs545954016	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12981497	ACTCGCGGTTAGGAG[C/G]TGGAGACCAGCCCGG	81929
rs546010546	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970380	GTGACTTCTGCAGGG[A/G]TAGTCTTTTCCACTT	81929
rs546045164	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12974066	TTTCAGCATCAAAAA[C/T]GAGGGGAAGTGGTGT	81929
rs546064400	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12954926	TTTACCACCTCTAAA[A/G]GAAACCCTGTGCTCA	81929
rs546145992	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12952307	GCGTGATCTTGGCTC[A/G]CTGCAACCTCCGCCT	81929
rs546152124	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12975004	TTTTATTTTATTTTT[A/T]TTTTTGAGATGAAGT	81929
rs546159891	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12960709	AGTTCAGTATACTAT[A/G]GATTGGATTTGGGAG	81929
rs546177890	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976288	TCTCATGAGGCAGGC[A/G]TCACAGGCTTGTGTG	81929
rs546189013	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12955758	TCCATGTTTTTTTCT[G/T]CCTTTTTTATTTCAT	81929
rs546212709	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12982173	ACCTGGCCTTGCCCT[A/G]CCTTTTTAAATTAAT	81929
rs546242232	in-del	-/CCCC			intron-variant	SEH1L	GRCh38.p7	18:12969225	CGCCCCCCCCCCCCC[-/CCCC]ACCTCACCAAAAAGA	81929
rs546303452	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947427	GCTCTTCAGCCGTCC[C/G]GACGGAGCGCGGCTC	81929
rs546566315	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954474	CTTTTGAAGCAAATA[A/C]TTTTTTTTTGGAGAC	81929
rs546640360	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12953536	CATTTTAGTAGTTGA[C/G]AAGTGACCACAAAAA	81929
rs546655053	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12961912	CCTCAAGTGATCACC[C/T]GCCTCAGTCTCCCAA	81929
rs546790600	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949144	AGTGCTGGGATTACA[A/G]GCGTGAGCCACCGCG	81929
rs546848076	snp	A/G	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12981661	TGCTTTATTTAGGCT[A/G]AAACTAACAATTCTC	81929
rs546882787	snp	C/T	0.00318978	0.0398085	intron-variant	SEH1L	GRCh38.p7	18:12981188	TCCTAGATGGGATGG[C/T]GGCCGGGCAGAGACG	81929
rs546913794	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12979218	GAGGACCCTGCGGCC[-/T]TCTGCAGTGTTTGTG	81929
rs546929207	snp	C/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12954972	TTGTTTACTCTGCTC[C/T]CAGCCGCTGGTAACC	81929
rs546987484	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12961166	GTTTACTGGAGTTGC[A/G]CAGATGCTCACTTGA	81929
rs547025359	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12965115	GCCTCCTGGTTCAAG[C/T]GATTCCCCTGCCTCA	81929
rs547025999	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12969465	GAGGCCGAGGTGGGC[A/G]GATCATGAGGTCAGG	81929
rs547147563	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12972108	ACATGGTGGATTCAC[A/G]GCTAGGATGCTATGA	81929
rs547479094	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971462	ATATGGTGAAACCCC[A/G]TCTCTACTAAAAGTA	81929
rs547491184	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986147	TCAAGATTTTCTTAA[C/T]TTAGTTCGCTGTTTA	81929
rs547709076	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12975936	CTTGTTGAGATGGGG[A/G]CTGAGCAAAGAGGAG	81929
rs547727065	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12967115	CAATTATCATTTGCA[C/T]TGGCAATGTTCTATA	81929
rs547751219	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12953539	TTTAGTAGTTGAGAA[A/G]TGACCACAAAAATCA	81929
rs547760699	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951920	GGTTAGTATTTATTT[G/T]TACATTTATTAAAAA	81929
rs547865974	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12966598	GTGGATATGGGGTTT[C/T]GCCTTGTTGCCCAGA	81929
rs547935084	snp	C/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949653	AGAGACAGGGTTTCA[C/G]CATGTTAGCCAGGAT	81929
rs548003123	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12967722	AGTTTGAGACTAGCC[C/T]GGCCAACACAGCGAA	81929
rs548118099	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952293	GTGGGAGTGCAGTGG[C/T]GTGATCTTGGCTCAC	81929
rs548124411	snp	C/G	6.74969e-05	0.00580895	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986840	TTTGTTTGGTGTTTT[C/G]TTCCTGTCTTCATTG	81929
rs548155932	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12969744	GAAAAAGGAAGTTTG[C/T]GGCCAGGTGTGGTGG	81929
rs548196686	in-del	-/GCCAATGGAAATGAGTTTTAATG	0.0023933	0.0345097	intron-variant	SEH1L	GRCh38.p7	18:12965769	TGATGGATTTTGATA[-/GCCAATGGAAATGAGTTTTAATG]GCCAATGGAAATGAG	81929
rs548241106	snp	A/G	0.039522	0.134904	intron-variant	SEH1L	GRCh38.p7	18:12973992	GGTGCTGGCGGCTGG[A/G]GTTTGGTCATCCAGC	81929
rs548389131	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12972014	TCCATTGTTTCAGTT[C/T]TATCTTACAGGTGAT	81929
rs548425417	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968372	ATGAACCATTGGGGC[A/G]CAGTTCCTTCCTCCC	81929
rs548555664	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12959528	ATTCGGTATGCTTCA[A/G]TAAGCATTTTCTTTG	81929
rs548625649	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12980803	ACCTCCCGGACGGGG[C/T]GGCTGGCCGGGCGGG	81929
rs548632347	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12976579	TGTCCTATTTCTGGC[C/T]TTTGGTAGAAGGCCA	81929
rs548634796	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12983221	TTGGATGATTATCCA[C/T]TAGGCAGAGATGTCT	81929
rs548669565	snp	C/T	1.94839e-05	0.00312115	intron-variant	SEH1L	GRCh38.p7	18:12982470	GTGTATATATATATG[C/T]TTTAAAACTTTGTTT	81929
rs548781288	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12960330	TCAGTCATTAAAAAA[C/T]GTTAGGGTGCTGAAA	81929
rs548875824	snp	C/T	0.00835141	0.0640778	intron-variant	SEH1L	GRCh38.p7	18:12957352	AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG	81929
rs548957025	snp	A/G	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12970614	TTTTTTTGTAGAGAT[A/G]GAGTCTTATTATGTG	81929
rs548961767	snp	A/T	0.000345955	0.0131475	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971228	GGCCAAGGTTCAGAT[A/T]TTTGAATATAATGAA	81929
rs549010174	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12966036	ATTATTATGTGTTGG[A/C]CTTTGTTGATTAATC	81929
rs549094665	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12976993	AAAAAAAAAAAAAGC[A/G]TATTCTGATTGTGTA	81929
rs549210923	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12963016	ATGTACTTGTAGGAA[C/T]TTGTGGCCCAGAGAT	81929
rs549211696	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955753	TTTCTTCCATGTTTT[C/T]TTCTTCCTTTTTTAT	81929
rs549363369	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971938	TACTGTTGTTGGAAC[A/G]TGCTGGGCAAAAATG	81929
rs549380822	in-del	-/AAAG	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12967938	AAAAAAGAAAAAAAA[-/AAAG]AAAGCCTGAGAGAAT	81929
rs549398877	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12984448	GTTTACAGGTTTAAG[A/G]TTCAACTTTGCTTCC	81929
rs549419362	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12960010	GTAGATTTTATGTGA[C/T]TAGATCTAGTAAGGG	81929
rs549539523	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12950777	TTTAACAGGTGAAAT[C/T]GGCACCTTCTTATTG	81929
rs549584076	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12977657	TGAACTCAGGAGGCG[G/T]AGGTTTCAGTGAGCC	81929
rs549624301	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12964987	TGCTTCCCCCTCACA[C/T]TGCCCCTTCCATTTC	81929
rs549625256	snp	A/G	1.66147e-05	0.0028822	intron-variant	SEH1L	GRCh38.p7	18:12978921	GCATTTATGAATTTG[A/G]AAATACTCTTGCCTT	81929
rs549625304	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12972146	CCAGGTGGGAGAGTA[C/T]GTGGCTTTGGGATAG	81929
rs549625750	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12980708	GCTGACACCCCCCAC[C/T]TCCCTCCCGGACGGG	81929
rs549661968	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12978424	TGCCTCTGTGTTCAC[A/G]TGGCTGCCTCCTCTC	81929
rs549665633	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12973592	GGTGTGAGCCACCAC[A/G]GCCGGCCTAGAAATT	81929
rs549725316	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12957196	ACTTTAGGAGGCCAA[A/G]ATGGACAGATCACCT	81929
rs549857074	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12977017	TTGTGTAGGCCCCAG[G/T]AGGGGGCTGAGATTC	81929
rs550007203	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12956780	TGCTTCAGAGTTTAG[C/T]GTAACCAACCTTTGA	81929
rs550041972	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12970343	CACAGATGAGTCTAG[G/T]GAGGGGAATGACGTG	81929
rs550135828	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12975188	GTAGAGATGGGGTTT[C/T]TCCATGTTGGTCAGG	81929
rs550137253	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947201	GCTTCCTTCCCCCGG[A/G]ATGACACGTTTCTAC	81929
rs550199131	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12950476	ATTGCTAATGTGTTA[A/C]TATTTATTGATTTCC	81929
rs550274406	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12952433	AGATGGGGTTTCGCC[A/G]TGTTGGCCAGGCTGG	81929
rs550292299	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951743	TTGCTGATTGTGTTC[G/T]TTTGTTAACTATATG	81929
rs550384432	snp	C/G	0.00279162	0.0372561	intron-variant	SEH1L	GRCh38.p7	18:12973610	CGGCCTAGAAATTAC[C/G]TAAGTATTTCTAAAT	81929
rs550424990	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12979692	GGTGGCTGGCTGGGC[C/G]GGGGGCTGACCCCCC	81929
rs550430031	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12966176	TGGCTCACTGCAAGC[G/T]CCGCCTCCTGGGTTT	81929
rs550469945	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12973077	TGTGGGGATGATGGC[A/G]CATGCCTGTAGTTCC	81929
rs550494009	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12961380	GCAACCAATGATTAG[C/T]TTAGAGAGAAAGTTT	81929
rs550598943	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948528	GGCTGCGGGCGGGAA[C/T]CCAGGGGCATCCCAC	81929
rs550737763	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948042	TCCCGGGCTGCGAGG[C/T]CTGGCTAGGCTACGG	81929
rs550751796	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12969132	GGAGAATCATTGAAC[C/T]TGGGAGGTAGAGGTT	81929
rs550801144	in-del	-/TTTTC	0.00419396	0.0456003	intron-variant	SEH1L	GRCh38.p7	18:12951844	AATATCTGCCTTTTA[-/TTTTC]TTATAGGTCTGGGAT	81929
rs550802107	in-del	-/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12970052	TTCTTAATTAGATAA[-/T]TTGATCTAATTACCT	81929
rs550821183	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12976528	GCCTGGATTCAAACA[C/T]GTTCTGGCTGCAGCA	81929
rs550822954	snp	A/C	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12969513	GCCAACATGGTGAAA[A/C]CTCATCTTTACTAAA	81929
rs550858149	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12975951	ACTGAGCAAAGAGGA[A/G]TGAATGTGGTAAGCA	81929
rs550904207	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949722	CCTCCCAAAGTGCTA[A/G]GATTACGGGCGTGAG	81929
rs550968868	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954996	GGTAACCACTAATCT[A/G]CTTTCTGTCTGTATG	81929
rs551043394	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12981756	TTAGTATTGAGACAG[A/T]CTTGTGAATAACATA	81929
rs551109666	snp	A/G			downstream-variant-500B	SEH1L	GRCh38.p7	18:12987849	TTAGAATGGACAGAT[A/G]TTGACTTTCAGTCTA	81929
rs551205025	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12983401	TAAAACCAGCCCAGA[C/T]CTTCCTTTCCTCAGT	81929
rs551318831	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970574	AACGGCACATGCCAC[C/T]ACACCAGGCTAATTA	81929
rs551426230	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12956103	AGGCTGGAGTGCAGT[A/G]GCACAATCTTGGCTC	81929
rs551468046	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12950754	AGTGTTATTGCCCTC[A/G]TTACATTTTTAACAG	81929
rs551611569	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12981397	AGATCACGCCACTGC[A/G]CTCCAGCCTGGGCAC	81929
rs551622128	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970019	TTACTGTAGCATTTT[G/T]TAGTTTGCCTGGTAC	81929
rs551638612	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12962153	GTAATCCTAGCAACT[C/T]GGGAGGCTGAGGTGG	81929
rs551684929	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12979978	CCTCACCTCCCGGAC[A/G]GGGCGGCTGGCCGGG	81929
rs551737582	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946808	TTGCAGGTTTCTGTG[A/C]AATCCATCAGGGGAC	81929
rs551817722	snp	A/C	0.00993419	0.0697739	intron-variant	SEH1L	GRCh38.p7	18:12981411	CACTCCAGCCTGGGC[A/C]CCATTGAGCACTGAG	81929
rs551818761	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12956321	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC	81929
rs551906362	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12967444	ACAGGGTTTTAAACT[A/G]TGAAATCACTTTTAA	81929
rs551996194	snp	G/T	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12977843	TTTTTTATTTTTTAT[G/T]TTTGCAGTTGAGTCT	81929
rs552088527	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12950261	GGCTAGTCTCGAACT[C/G]CTGAGCTCAAGTGAT	81929
rs552133272	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12953029	TCAAGTGATCCGCCC[A/G]CCTTGGCCTTCCAAA	81929
rs552147286	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12960409	TGAATGGTCTTGACA[C/T]CTTTGTTGAAAATAA	81929
rs552153099	snp	A/G	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12969416	AAATCTTGGCCAGGC[A/G]TGGTTGTTTACGCCT	81929
rs552190172	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968569	TCTGGAATTTTCTAC[G/T]TACTGATGGTGATAC	81929
rs552221993	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12959254	ATCCCTTATCTGTTA[C/T]AGGTTGAGTATTCCT	81929
rs552398112	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974539	CACCTCAGCCTTCCA[A/T]AGTGCTGGGATTACA	81929
rs552411038	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12961105	GGTGGGCAGTCCGCA[C/T]GTGCAGTGGCCCACT	81929
rs552603876	in-del	-/TTTTA	0.00175033	0.0295314	intron-variant	SEH1L	GRCh38.p7	18:12951839	TATAAAATATCTGCC[-/TTTTA]TTTTCTTATAGGTCT	81929
rs552650708	snp	A/G	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12981177	CGCTCCTCACTTCCT[A/G]GATGGGATGGCGGCC	81929
rs552722076	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948569	GGCGTCGTGGGTCTT[C/G]CCCGCGCTGTTCACC	81929
rs552740458	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12962353	TACTCCAGCCTGGGT[A/G]ACAGAGCAAGACCCT	81929
rs552870007	snp	A/C			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985356	CGCCGTTTGACCTCT[A/C]CCAAGATACACCAGC	81929
rs552903487	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959966	AGGGCAAGATCTCTC[A/G]AATCCATCTAAACAA	81929
rs552940148	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12957525	AGAACATAATATAAT[A/C]TGTGTGCTGTTGAAG	81929
rs552955909	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12967564	CTTCTGCTGGGAAAC[C/T]GCATCAGGCAACTGG	81929
rs552965621	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12953904	TTTGCTTAACTAGTG[A/G]ATATTTCAGTTTCCA	81929
rs552997243	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974086	GGAAGTGGTGTTGGG[A/G]AAAGAGTGTCTGCAG	81929
rs553000534	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12953349	TGTAGACATATATTT[C/T]CATTTCTTTTGGATA	81929
rs553000602	snp	A/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12960541	TAGCTTGAGTGGCTA[A/T]TCAGACTGTTTTACA	81929
rs553046466	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12980338	CAGAGGCGCCCCTCA[C/T]CTCCCGGACAGGGCG	81929
rs553069808	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946942	GCCTCATTTTTTTTT[C/T]TTCTGTACTTTCGCT	81929
rs553083310	snp	A/G	1.69072e-05	0.00290746	utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987058	AATGAAGGGATTTAA[A/G]ACACTGATTTAACAT	81929
rs553163467	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968020	ATCTCTAAATAGTGA[C/G]GATTGGCTATATGTG	81929
rs553188637	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12975423	AGGATATGGATGAGG[A/G]TGGTCACCTGCTAGA	81929
rs553190578	snp	A/G	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12981911	GTTGCCCAGGCTGGA[A/G]GGCAGTGGCTTGATC	81929
rs553229479	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12981375	AGGTGGAGGTTGTAG[C/T]GAGCCGAGATCACGC	81929
rs553299217	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12975281	ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCACCTT	81929
rs553306884	snp	C/G	2.01424e-05	0.00317345	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948270	GGGCCGACCCCGGAA[C/G]GAAGGAAGGGGAGTG	81929
rs553308129	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12980890	CCCCCCCCACCTCCC[G/T]TCCGGACGGGGCGGC	81929
rs553386953	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12956885	AACATGGCTAACATG[A/G]TGAAACCCTGTCTCT	81929
rs553423685	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12964098	ATATATTAATATATC[C/T]AGTCTTACCTCATTT	81929
rs553423875	snp	G/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12955988	TAGGCATGAGCCACT[G/T]TGCCTAACTCTAAAA	81929
rs553593472	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12978181	GAGCTAAATGTACAT[C/T]ATTAAAGGAGGAAAC	81929
rs553628721	snp	G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12984745	ATAAGGAATATTTGA[G/T]GTCATCTAGAGTCTG	81929
rs553766205	snp	A/G	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12950316	GCTGGGATTACAGGT[A/G]TGAGTCACCTTGCCC	81929
rs553776938	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12970723	AGCCACCCTGCCGCA[A/G]TGTTTCTTCTTTTTG	81929
rs553795234	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12980841	CCCCCCCACTTCCCT[C/T]CCGGACGGGGCGGCT	81929
rs553855344	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12978535	ATTCTGAGGTCCTTA[A/G]TTACATTTTCAAAGA	81929
rs553939187	snp	C/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12973885	ATGATCACAAAAGAG[C/T]TGCACAATGTCAGGT	81929
rs553951749	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12975610	GAGAGAGACAGGGGA[A/G]GGGCAGGCCAACAGG	81929
rs554125516	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12966211	GATTCTCCTGCCTCA[A/G]CCTCCTGAGTAGCTG	81929
rs554159705	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951565	CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGACG	81929
rs554187309	snp	G/T	0.00896121	0.0663348	intron-variant	SEH1L	GRCh38.p7	18:12984243	TTTTAAATCATTCTG[G/T]TAGCCATACTTAAGG	81929
rs554197589	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12957533	ATATAATCTGTGTGC[A/T]GTTGAAGTTCCTCAT	81929
rs554225709	snp	A/G	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12968060	ATATCAGTTCTTTTC[A/G]TGTGCCTTGGTCTTT	81929
rs554301255	in-del	-/TT	0.0733698	0.176923	intron-variant	SEH1L	GRCh38.p7	18:12955441	GTATCTGTTCTTTTC[-/TT]TTTTTTTTTTGATTC	81929
rs554349980	snp	A/G			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949081	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCGT	81929
rs554382409	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12979163	GGAGGGAAGGTCAGC[A/G]GATAAACAAGTGAAC	81929
rs554383411	snp	A/G	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12952422	GTTTTTAGCAGAGAT[A/G]GGGTTTCGCCATGTT	81929
rs554420085	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952105	GTAATTCTGTAGCAT[A/T]CTAACATAATTATCT	81929
rs554457184	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12957960	GCAATCCTCTCACCT[C/T]GGCCTCCCAAAGTGC	81929
rs554661112	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12965292	GCTGGGATTACAGGC[A/C]TGAGCCACCTCGCCC	81929
rs554695889	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12958001	GGCGTGAGCCACTAC[A/G]AGGGCCATGATGCAA	81929
rs554732661	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12966337	GCTCAGGTGATTTGC[C/T]GGCCTCGGCCTCCCA	81929
rs554886753	in-del	-/TTTTTTTTTT			intron-variant	SEH1L	GRCh38.p7	18:12981868	TTTTTTTTTTTTTTT[-/TTTTTTTTTT]GAGGCAAGGTCTCAC	81929
rs554939776	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12958711	CTGAGTAATATTCCA[C/T]TGTGTGTGTATACCA	81929
rs554956211	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12966969	AATGGCAATCATTTT[G/T]AATTGTTCAGAGTTT	81929
rs554996266	in-del	-/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12954789	AATGAAAAAAAAGTA[-/T]TTTTTTGATTGAGCT	81929
rs555098055	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12982416	TGGCGAGACCACTTG[C/T]ATTAATTTAGAATTT	81929
rs555218546	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946988	TCCACTGTCTCCCAT[C/T]CTAACTTTACCACTA	81929
rs555280863	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12958672	CCATTTTGTAGCATA[A/T]ATTAACTTTATTCCT	81929
rs555403890	snp	A/G	0.00438332	0.0466095	intron-variant	SEH1L	GRCh38.p7	18:12969596	GGGAGGCCGAGGCAC[A/G]AGAATCGCTTGAATC	81929
rs555554111	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12983858	AAAACTTCTAAAAAG[G/T]TGTTAAAACTGAGAT	81929
rs555614584	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949332	ACATTCGAGTTTGAT[A/G]CCAGTGATCTCTCAA	81929
rs555652406	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12974927	TTATTTACACTCTCA[C/T]TGAGGATCTTATTTG	81929
rs555674764	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12956993	GAATGGTGTGAACCC[A/G]GGAGGCGGAGCTTGC	81929
rs555838494	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12977247	GGGAGATGTCTCCAC[C/T]CAGTCTCCTACATGC	81929
rs555850649	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970265	AAAAAGTCATTCAGC[A/T]TATAGTTCAGGAGAG	81929
rs555882256	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955868	TTGTATTTGATTTTA[C/T]CTATTAGTATATTTT	81929
rs555910336	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12982826	TTGAACATCAGTTTA[A/C]CTAGTTCATAGAAGT	81929
rs556096190	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12977920	TGCAACCTCCGCCTC[C/T]TGGGCTCAAGCCATC	81929
rs556098013	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971022	TCAGCTATGTGGCAG[A/C]GACCTAGATTCACTA	81929
rs556155133	snp	C/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12955300	AATTTAACTTTTTAT[C/T]TACATGTTATGTTGA	81929
rs556213470	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968085	GTCTTTATCTTCTGC[A/G]CCACTTGTTTTTCTT	81929
rs556284026	snp	C/T	1.65773e-05	0.00287895	intron-variant	SEH1L	GRCh38.p7	18:12984032	GTATTTGATTATTTT[C/T]CTTTCAGCTAATTAT	81929
rs556337414	in-del	-/T	0.464947	0.127663	intron-variant	SEH1L	GRCh38.p7	18:12973307	AATAGAAATTACCTA[-/T]TTTTTTTTTTTTTTG	81929
rs556364708	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12978058	GTCTTGAACTACTGG[A/G]TTCAAGCAATTCTCC	81929
rs556403287	snp	C/G	0.00517822	0.0506191	intron-variant	SEH1L	GRCh38.p7	18:12984662	CTTTAATAGAAATAA[C/G]AGGAAATAATAAAAC	81929
rs556581819	snp	C/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948485	GCCCGCAGGGTACGC[C/T]GGGCCCTCTCCCAGG	81929
rs556637753	snp	C/T	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12977289	TGCTGCCGTTCTGTC[C/T]AGGATATTCAATCTT	81929
rs556638598	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971618	CAGGCTGGGCAACAA[C/G]AGCGAAACCCTGCCT	81929
rs556724364	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12953737	CATTTACTTCATTTA[C/T]AGTGTTGTGTAACTA	81929
rs556802267	snp	A/G	0.00438332	0.0466095	intron-variant	SEH1L	GRCh38.p7	18:12980461	GGGGCGGCTGGCCGG[A/G]CGGGGGGCTGATCCC	81929
rs556865546	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12966382	CAGGCGTGAGCCACC[A/G]CACCCAGCCACCATT	81929
rs556954150	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948829	TCTGTAGACACTTCC[G/T]ACAAGCAGAATTTCT	81929
rs557006262	snp	G/T	0.00755907	0.0610114	intron-variant	SEH1L	GRCh38.p7	18:12980990	CTTCCCAGACGGGGT[G/T]GCTGCCGGGCGGAGG	81929
rs557042670	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974686	TGAAAATACTAAAAC[A/G]GATCTAGGATTGATA	81929
rs557130819	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954606	CAAGCAGCTGGGACC[C/G]TAAGTGCATACCACC	81929
rs557153968	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12960577	TCTCAGGGGAGGAGT[A/T]TGTCTGATTGCCTTT	81929
rs557181307	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12969659	TGCCACTGCACTCCA[A/G]CCTGGCGACAGAGTG	81929
rs557217921	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976233	TTGTGTCCTCACAGC[A/G]TGGCAGCTGCTTCTG	81929
rs557658166	snp	C/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12982062	GTAGGGATGGGGTTT[C/T]GCCATGTTGGCCAGG	81929
rs557680378	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12981035	CAGACGGTGTGGCTG[C/G]CGGGCGGAGGGGCTT	81929
rs557832745	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968981	TTTGAAAGGCTGAGG[C/T]GGGCAGATCACCTAA	81929
rs557854039	snp	G/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12981329	GAGGCTGCAATCTCG[G/T]CACTTTGGGGGGCCA	81929
rs557931191	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949288	ACTCCAGAGTAACTG[C/G]AAATCTGAAGGATAG	81929
rs557966999	snp	A/G	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12954706	CCCCTGGGCTCAAGC[A/G]GTCTGCCCACCTCAG	81929
rs558125148	snp	A/G	0.00597247	0.0543191	intron-variant	SEH1L	GRCh38.p7	18:12962043	ATGTTGGAATTTTAC[A/G]GTGATCATAAAGCTT	81929
rs558150539	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946037	ATGCATATTACTATA[A/C]GGAAAGAAGCCAATC	81929
rs558160356	snp	A/C	0.00795532	0.062565	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946530	CACTCCCACTCTGAT[A/C]ATCTCTGGCAACCAA	81929
rs558319286	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12978082	ATTCTCCCACCTCAG[C/G]CTCTCAAAATGCTGG	81929
rs558379771	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12966380	TACAGGCGTGAGCCA[C/T]CGCACCCAGCCACCA	81929
rs558397021	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970382	GACTTCTGCAGGGGT[A/G]GTCTTTTCCACTTTT	81929
rs558432041	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976704	GGCGCAGTGGCTCAC[A/G]CCTGAATCCCAGCAC	81929
rs558451877	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12958758	TCATTTGTAGATGGA[C/T]CCTTGGGTTGTTTCT	81929
rs558494068	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12983671	TAATTAAGAAGACAA[C/G]TTCATTACCTTACAT	81929
rs558564499	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12959550	TTTTCTTTGAGCATC[A/G]TGCCAGTGCTCAAAA	81929
rs558602050	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12958823	CATTGTTGTACAGAT[A/G]AATGTTTGAGACCGT	81929
rs558637156	snp	A/C	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12967383	CATAAGGCACATCCC[A/C]GCCTTCCTATGTTTA	81929
rs558761648	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974038	AGAGAGTGAGACAGC[A/T]AGTGTCTGGCATTTT	81929
rs558797727	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12980064	CCTCCTGGACGGGGC[A/G]GCTGGCCGGGCGGGG	81929
rs558857380	snp	A/C			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947664	CCCTCCGCCGCCGAA[A/C]GGTCAGAGCCTGGAG	81929
rs558905423	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948121	GGGCCCGACGGAAAC[C/T]ATGTTTGTGGCTCGC	81929
rs559111226	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952834	TCGCCCAGGCTGGAG[C/T]GCAGTGGTGCGATGT	81929
rs559120465	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12967406	TATGTTTAGGAACAC[C/G]AGACAGCACTTCAGC	81929
rs559127603	snp	A/G	0.00279162	0.0372561	intron-variant	SEH1L	GRCh38.p7	18:12965769	ATGATGGATTTTGAT[A/G]GCCAATGGAAATGAG	81929
rs559147979	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12958993	GTTCCAGTTTTTCCA[A/G]ATCTTCATCAGCACT	81929
rs559151898	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952254	TTTTTTTTTTGAGAC[A/G]GAGAGTCTTGCTCTC	81929
rs559159800	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12972864	TAAAGTAAATTTCAA[C/T]CTGAGCTGAGCAGAA	81929
rs559165389	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947510	GTCTGGGGGGAAACA[C/T]ATCCAAACGTCGACT	81929
rs559273634	snp	C/T	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12980716	CCCCCACTTCCCTCC[C/T]GGACGGGGCGGCTGG	81929
rs559324262	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12969917	AAAAAACGCAAAAGG[A/G]AGTTTGTGAGACACA	81929
rs559336403	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12957367	CGGGAGGCGGAGGTT[G/T]TGATGAGCAGAGATC	81929
rs559337628	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12973516	TGTTGGCCAGGCTTG[C/T]CTTGAACTCCTGACC	81929
rs559429157	in-del	-/TG	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12982748	TTAAAATGTAAACTC[-/TG]AAATATTTTTTGAAA	81929
rs559459634	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12979484	TTTCTACACAGACAC[A/G]GCAACCATCCGATTT	81929
rs559503584	snp	C/T	1.64762e-05	0.00287016	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978817	ATATTGCATTCGCTC[C/T]AAATTTGGGAAGATC	81929
rs559634312	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974367	TCGCTTCAACCTTTG[C/T]CTCCCGGGTTCAAGC	81929
rs559672481	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12983168	TCTGGTCAGTTGACA[C/G]TGACTGTGGTCTCTG	81929
rs559735800	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12975375	CATAAGCAGCATGGA[C/G]TGTACTAAGAGCTGA	81929
rs559785206	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	SEH1L	GRCh38.p7	18:12987742	TACTCTTCTTTCACT[A/G]TCTCACAAAAAACCC	81929
rs559935079	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968365	GAGCACGATGAACCA[C/T]TGGGGCGCAGTTCCT	81929
rs560018856	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12952531	CACTGTGCCCGGCCA[A/T]GTAGAAATTTTCATA	81929
rs560039073	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12964322	TAATTCTGGTAGTCA[C/G]TAGTATATTTTTAAA	81929
rs560042323	in-del	-/TA	6.78196e-05	0.00582282	intron-variant	SEH1L	GRCh38.p7	18:12963146	AATTTAAATTGTTAT[-/TA]TTTTTTTTTTAGGTT	81929
rs560167429	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12977421	TGCATAGTTTCCTTT[C/T]ATTATCACTTAACTC	81929
rs560277285	snp	A/G	0.00597247	0.0543191	intron-variant	SEH1L	GRCh38.p7	18:12951184	CATTGAGGTGAAACC[A/G]GGCGATACTCTATTT	81929
rs560405023	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12976845	GCCGGGCGTGGTGGC[A/G]GGCCCCTGTAGTCCC	81929
rs560410093	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976940	GAGATCACACCACTG[C/T]ACTCCAGCCTGGGCG	81929
rs560497805	snp	G/T	0.00517822	0.0506191	intron-variant	SEH1L	GRCh38.p7	18:12957120	TTTGTGGTTACTTTT[G/T]TTTTCTTAGGAAATA	81929
rs560524550	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948718	AAGCTCACTTTGTTA[C/G]GCCGAGGAAGAAAAA	81929
rs560567929	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12968681	CTAATGGCACTCTTT[C/G]TAGATTTCTAGCCCT	81929
rs560569404	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12963896	TTTTGCATTTTTAGT[A/G]GACATGGGGTTTTAC	81929
rs560640802	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971780	ACCTGGGGAACCTAA[C/T]CTGGTTTAGGGGCTA	81929
rs560717348	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951651	TTGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC	81929
rs560722784	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12959357	TACCAGTTAAGCATT[C/T]GCCTACTTATTTATT	81929
rs560755878	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12985016	ATGCATCAAAACAAT[A/T]TCAGGTTACCGTGGA	81929
rs560817883	snp	A/C	1.72027e-05	0.00293275	intron-variant	SEH1L	GRCh38.p7	18:12984255	CTGGTAGCCATACTT[A/C]AGGTGGATTATTTCA	81929
rs560835163	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971847	AGAAGTTAGCCAGAC[A/T]AAGAGGGCAGAAGCA	81929
rs560871783	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12978218	GGTTGTATTAATTTC[C/T]TAGGGCTGCCATAAC	81929
rs560903005	snp	G/T	0.0023933	0.0345097	intron-variant	SEH1L	GRCh38.p7	18:12984793	TAAATATGTGAATTT[G/T]TAAGATAAAATTATT	81929
rs561090166	in-del	-/A	0.0023933	0.0345097	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946841	TGGGACTAATCATTT[-/A]AAAAAACTTTCCAGC	81929
rs561299601	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12951690	GCCATCGCACCCAGC[C/T]TCTCAATAAATACTT	81929
rs561339766	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12960515	ACACTGTTTTAATTC[C/T]GGTAGCTTTGTAGCT	81929
rs561461215	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12983665	CTTGCATAATTAAGA[A/G]GACAACTTCATTACC	81929
rs561464578	in-del	-/TAAT			intron-variant	SEH1L	GRCh38.p7	18:12962941	TTTCATTAAAGGGAG[-/TAAT]TAATTATAGCTCACT	81929
rs561494838	snp	A/G	0.00438332	0.0466095	intron-variant	SEH1L	GRCh38.p7	18:12979582	CTCAATGAGCTGTTG[A/G]GTACACCTCCCAGAC	81929
rs561566831	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12978952	CTGATTACCTTTGTT[C/T]GTGGAGGAGAGAGTA	81929
rs561596014	snp	A/C	0.00835141	0.0640778	intron-variant	SEH1L	GRCh38.p7	18:12960966	AAATGAAGTAAAATA[A/C]ATTTGGAAGAGGGCC	81929
rs561658942	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948516	CCGCGCTGCCGGGGC[A/T]GCGGGCGGGAACCCA	81929
rs561731715	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12953577	TTGATTTGTATTTCC[C/T]TAATACCTCATGTTG	81929
rs561826350	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12960168	GCAACATTTTTCTTT[A/C]CATGACGCTGAAGTT	81929
rs561918505	snp	G/T	0.212425	0.24716	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949028	CTAATCTTTTTTTTT[G/T]TTTGTATTTTTTAGT	81929
rs561939783	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12950421	TTAATTGAGCAAGTA[A/G]TATATTTTTCTTTTT	81929
rs561962656	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12981664	TTTATTTAGGCTGAA[A/G]CTAACAATTCTCCAA	81929
rs561973732	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12956138	CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT	81929
rs562045826	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12962631	ACCACCACACCTGGC[-/T]TTTTTTTTTTTTTTA	81929
rs562140409	snp	A/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12976800	AAACCCTGTCTCTAC[A/T]AAAAAATACAAAAAA	81929
rs562196521	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12969826	GAACCCAGGAGGTGG[A/G]GGTTGCAGTGATCAG	81929
rs562340850	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949576	TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGGGACT	81929
rs562478032	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974353	GGCGCAACCTTGGCT[C/T]GCTTCAACCTTTGCC	81929
rs562500638	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12976869	TAGTCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG	81929
rs562502094	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949061	AGACAGAGTTTCACC[A/G]TGTGGGCCAGGCTGG	81929
rs562540802	snp	A/G	0.00835141	0.0640778	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948531	TGCGGGCGGGAACCC[A/G]GGGGCATCCCACCGT	81929
rs562610389	snp	C/T	0.00835141	0.0640778	intron-variant	SEH1L	GRCh38.p7	18:12954317	AGCCACCTCCCCTCC[C/T]ACCCCTTGGCCAACA	81929
rs562637802	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12983066	AATCCAGTATCTTCC[A/C]TGCTTCTTCTCTGCA	81929
rs562722912	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12971574	AGGAGGCGGAGGTTG[A/C]AGTGAGCTGAGATTG	81929
rs562797702	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976547	CTGGCTGCAGCATGT[A/G]TGCTCTTAGCTCCAC	81929
rs562832452	snp	A/G	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12982449	CGTGTGTATATATAT[A/G]TGTGTGTGTATATAT	81929
rs562888623	in-del	-/T	0.48714	0.0791489	intron-variant	SEH1L	GRCh38.p7	18:12955442	TATCTGTTCTTTTCT[-/T]TTTTTTTTTTGATTC	81929
rs562927661	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12970368	GACGTGGGGATCGTG[A/T]CTTCTGCAGGGGTAG	81929
rs562953092	snp	A/G	1.65644e-05	0.00287783	intron-variant	SEH1L	GRCh38.p7	18:12971111	GTGAATGAAATGTGT[A/G]TTTCTTTTGTTATCT	81929
rs562990344	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970520	CCAACTCCTGGGCGC[A/G]AGTGATCCTCCTGCC	81929
rs563028729	in-del	-/AAAAAAA/AAAAAAAA	0.465996	0.12588	intron-variant	SEH1L	GRCh38.p7	18:12971634	GCGAAACCCTGCCTC[-/AAAAAAA/AAAAAAAA]AAAAAAAAAAAGAGG	81929
rs563050535	snp	A/G	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12956280	CGATCTCCTGACCTC[A/G]TGATCTGCCTGTCGG	81929
rs563120477	snp	G/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949460	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTGAGAC	81929
rs563130643	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951086	GAAATTTACTTGTAC[C/T]CCAAAAGTCACACTG	81929
rs563135994	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947640	AGGTAACTCGCCTTT[G/T]GCAGAGCACCCTCCG	81929
rs563180288	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12958366	GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCT	81929
rs563301197	snp	A/G	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12975062	CAATGGTGTGATCTC[A/G]GCTCACCGTAACCTC	81929
rs563317372	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12967636	ATGAAAGCCTGGGCC[A/G]GGCACAGTGGCTCAC	81929
rs563340252	in-del	-/ATTTCAG	0.00279162	0.0372561	intron-variant	SEH1L	GRCh38.p7	18:12959584	TTTGGAGTTTGGAGC[-/ATTTCAG]ATTTCAGATTTTTGG	81929
rs563354143	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12966531	CAGCCTCCCAAGTAA[C/T]TGGGACTACAGGCAT	81929
rs563359910	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974160	AAGTTCAGCACTTTT[C/T]GGAGTTCTGTTGCTG	81929
rs563371304	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12953440	TCTTCCAAAGTGGCT[G/T]TGCCCACCAGCCATG	81929
rs563438504	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12951591	AGACGGGGTTTCACC[A/G]CGTTGTCTAGGCTGG	81929
rs563477759	snp	C/G			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948600	CGACGACCTGCAGTG[C/G]GACCTGGTGGGAGAC	81929
rs563626561	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12969210	GCAAAACTCTGTACC[C/T]GCCCCCCCCCCCCCC	81929
rs563658447	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968477	TCTCACTAAGACAAT[A/G]TTTTTTGACCAAATC	81929
rs563658570	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12975484	AGAAGTTTCAGCTGA[A/T]GATGTTTGAGCATGA	81929
rs563732237	snp	A/G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12951299	AAATGGCCTCCAAGC[A/G/T]TAGTGACTGTAACTA	81929
rs563799946	snp	C/T	0.00478085	0.0486577	intron-variant	SEH1L	GRCh38.p7	18:12981148	ATCTCAGATGATGGG[C/T]GGCCGGGCAGAGACG	81929
rs563951462	snp	G/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12961034	TCTTGGACTTGGGTT[G/T]TTACACGTTGGCATG	81929
rs564117515	snp	G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12960031	CTAGTAAGGGAGGGG[G/T]AGTTTCACAGAATCC	81929
rs564135544	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12959331	GATTTTGCAATATTT[G/T]CATTTATACTTACCA	81929
rs564163360	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948416	TGGGGTCACGGCGGC[C/G]TCGCGGGCCGCCCTC	81929
rs564173332	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12967688	GGAGGCTGAGGCGGG[C/T]GGATCACTTGAAGTC	81929
rs564227428	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12981183	TCACTTCCTAGATGG[G/T]ATGGCGGCCGGGCAG	81929
rs564305782	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12978679	CAGTGTGAAAAAAAG[A/G]TGAGATGCAGTGATG	81929
rs564329909	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955346	CATAGAAGTAAAACT[A/G]TATTCTGTTTCCTGA	81929
rs564365531	snp	A/C	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12976383	CACGGGCCCCACTCA[A/C]ACTCATGGGGAGGAG	81929
rs564366968	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12954931	CACCTCTAAAGGAAA[C/G]CCTGTGCTCATTTAG	81929
rs564368085	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12962571	CCCACTGGCTCAAGC[A/G]ATCCACCCGCCTCAG	81929
rs564379591	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947748	ACGAGCCGGGAACAG[A/G]GCGGGGCTTGAGGGG	81929
rs564404447	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12961824	GGCGCCCGCCACAAT[A/G]TCTGGCTAATTTGAA	81929
rs564481481	in-del	-/AA			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946569	TTACTGTCTGTATTT[-/AA]ATTTAATTAAAACAA	81929
rs564499509	snp	A/G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12971986	GCAAGACTTGTATCT[A/G/T]TAAGAAGTAATGTCC	81929
rs564503811	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12956137	GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC	81929
rs564585034	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	SEH1L	GRCh38.p7	18:12975744	TTAGGGAGATGACTT[C/T]GGCAGCTGTGTGGAC	81929
rs564588296	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12981612	TTTTGGAAAGGGGAA[C/T]TGAGTCAAGAGCAGA	81929
rs564632643	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12968861	ATCTTAGTTCTGGTT[A/G]TACAATTGAGGTAAT	81929
rs564676370	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12968939	TATTTTTAAGGCCAG[C/G]TGGGGTGGCTCACGT	81929
rs564759181	snp	C/G			missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984129	CAGGGAACCTCAAAT[C/G]CTTCCCTAGGTTCAA	81929
rs564823633	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12965647	TATTAACGAGCTGTC[A/G]TCAGTCTGATGCTGG	81929
rs564856441	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12978694	GTGAGATGCAGTGAT[G/T]TGTGGATTTTTGCAC	81929
rs564892416	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986716	TTAGTTTTGGCATGA[A/G]TATACTAAAGCTTTT	81929
rs564980371	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12957604	CTTTCCAGCATTTTC[A/C]TATGAAGGTATTATC	81929
rs565188870	snp	C/G	0.00279162	0.0372561	intron-variant	SEH1L	GRCh38.p7	18:12973398	TCTACCTCCCGAGTT[C/G]AAGTGATTCTCCTGC	81929
rs565206137	snp	C/G	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12972830	ATTTTATAGAGGCTT[C/G]ATGAAGTGTTGGGCT	81929
rs565247130	snp	A/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12951753	TGTTCTTTTGTTAAC[A/T]ATATGTTCACCGCTT	81929
rs565255941	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987500	CTGACTAGTATGTAA[A/C]ATAAATCATTCCTGT	81929
rs565405901	snp	C/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947575	TCTTCACTTTTTCAT[C/T]TTTCTTCATTTGCAC	81929
rs565418906	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12973840	TTTTTCTTGCTGTCA[C/T]GCTTAGTACACTGGT	81929
rs565430919	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12963541	CCTGTTTTCACTCAA[C/T]AGAGGAAGCCGGCAT	81929
rs565454870	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12979818	ACTTCCCAGTAGGGG[C/G]GGCCGGGCAGAGGCA	81929
rs565493635	in-del	-/AT			intron-variant	SEH1L	GRCh38.p7	18:12965384	GTAAACATTTAACAC[-/AT]GTGTAAGTATTTTGT	81929
rs565589096	snp	C/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986078	ACTATTAAGAGAAGC[C/T]ATTAAAATTTTACTA	81929
rs565641187	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951477	CTCACTGCGACCTCC[A/G]CCTCTGGGGTTCAAA	81929
rs565642525	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12981898	AAGGTCTCACTCCGT[G/T]GCCCAGGCTGGAGGG	81929
rs565654150	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12964149	GCATGACTATATGAA[C/T]ATTACCATAGTTGCT	81929
rs565690570	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12955891	TATATTTTATGATAG[C/T]AATATATGATTTTAA	81929
rs565748022	snp	A/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12965141	CCTCAGCCACCTGAG[A/T]AGCTGGGACTACAGG	81929
rs565825471	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12979905	CTTCGCGGACGGGGC[A/G]GCTGGCCGGGCAGAG	81929
rs565875010	in-del	-/C			intron-variant	SEH1L	GRCh38.p7	18:12953657	AGGTCTATCCAAGGT[-/C]CCCCCCCCTTTTAAG	81929
rs565899060	in-del	-/C	0.00279162	0.0372561	intron-variant	SEH1L	GRCh38.p7	18:12975621	GGAGGGGCAGGCCAA[-/C]CAGGCCAGGCAGATT	81929
rs566077648	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986785	TCTTTGTATTTACTA[C/T]TTTTCTCTTTTTCTT	81929
rs566187957	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12957081	CAAAAAAAAAAAAAA[A/T]TCTATAAAAATTGTT	81929
rs566319713	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12952439	GGTTTCGCCATGTTG[C/G]CCAGGCTGGTCTCAA	81929
rs566414439	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12969559	TGGGCGTGGTGGCGC[A/G]TGCCTGTAATCCCAG	81929
rs566549806	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976055	AATAGCTGAGATTAG[G/T]TGTCTATTGCTGCAT	81929
rs566613843	in-del	-/A	0.475259	0.108435	intron-variant	SEH1L	GRCh38.p7	18:12957066	AGCGAGACTTGTCTC[-/A]AAAAAAAAAAAAAAT	81929
rs566754492	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12962155	AATCCTAGCAACTCG[A/G]GAGGCTGAGGTGGGA	81929
rs566812059	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12972509	GAGAAGAGAGCACTT[C/G]TCAGGTGATCAGATG	81929
rs566903435	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12971516	GCAGGTGCCTGTAAT[C/T]CCAGCTACTCGGGAG	81929
rs566976743	snp	A/G	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12955698	CAGATAATTGGTAAA[A/G]TATCACCACTCCCCT	81929
rs567429762	snp	A/C	0.00318978	0.0398085	intron-variant	SEH1L	GRCh38.p7	18:12955759	CCATGTTTTTTTCTT[A/C]CTTTTTTATTTCATT	81929
rs567499339	snp	C/T	0.00478085	0.0486577	intron-variant	SEH1L	GRCh38.p7	18:12956683	TAATGCTTCTGAAGT[C/T]CAGTTCTTCTGACAT	81929
rs567767381	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12950782	CAGGTGAAATTGGCA[C/G]CTTCTTATTGTAATC	81929
rs567905436	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12956655	TTTAGAAGACATTCT[A/G]TATTTAGGATTGTAA	81929
rs568034579	snp	C/T	0.0240643	0.107019	intron-variant	SEH1L	GRCh38.p7	18:12980897	CACCTCCCTTCCGGA[C/T]GGGGCGGCTGGCCGG	81929
rs568091097	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947942	GGGCCGGTGGGTGGG[A/G]CGGGGCTTGAAGGAC	81929
rs568115038	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947443	GACGGAGCGCGGCTC[C/G]TGACCAAACCCACGG	81929
rs568162720	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954501	AGACAAGTTCTTGCT[C/T]TGTCACCCAGGCTGG	81929
rs568222560	snp	A/G	0.00119737	0.0244387	intron-variant, splice-donor-variant	SEH1L	GRCh38.p7	18:12975883	CCAGCTGTAGGTCAC[A/G]TGAGTCTTGGTTTCT	81929
rs568270689	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12973953	AACACCTTTCCTAGA[A/G]GTATCTTAGCAGGCT	81929
rs568318000	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12950700	TGCTATTTTGCAGGT[C/T]GTACCGTTTTATACC	81929
rs568383010	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949186	AGCAGAATTTCTAAT[A/G]TGGGGATGCTACATG	81929
rs568398200	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12977821	TAGTGGCTAATAAAT[C/G]AAGCCCTTTTTTATT	81929
rs568407066	in-del	-/TCT			downstream-variant-500B, cds-indel	SEH1L	GRCh38.p7	18:12987551	ATGTGGACTTTTTGG[-/TCT]TTTTTTTTTTTTTTT	81929
rs568445292	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12961306	TTATCAGGAAGCTGC[G/T]GATCACCAGTTTCAG	81929
rs568534503	snp	A/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982530	CAGGAAAGAACTGAC[A/T]TCCTCTGGTGGGCCA	81929
rs568825509	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12975359	CACTTTTTCAACATT[C/T]CATAAGCAGCATGGA	81929
rs568925554	snp	C/T	0.00557542	0.0525036	intron-variant	SEH1L	GRCh38.p7	18:12981268	CAGACGATGGGTGGC[C/T]AGGCAGAGACGCTCC	81929
rs568948289	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12977543	CAGCCTGACCAACAT[G/T]GTGAAACCCTGTCTC	81929
rs569060452	snp	G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12957650	TTCCCCCTTTATGAT[G/T]TGTTTTTTGTAATAG	81929
rs569204395	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949252	ATGAAAGCTGGAGTG[C/T]GGATTATTTGGTTCT	81929
rs569237108	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955009	CTACTTTCTGTCTGT[A/G]TGGATTTTGGAGCAA	81929
rs569306122	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12977032	GAGGGGGCTGAGATT[C/T]TGGATTTCCCAGAAG	81929
rs569357670	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951967	GTTTATTTTATAGTT[A/G]TCTATGAATTGTTTT	81929
rs569396743	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12962019	GCCAGAAGATAACTT[A/T]TAAATGTGATGTTGG	81929
rs569491730	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12984703	TTTTTAGAATATTTA[G/T]CATATGTTACATTCT	81929
rs569542139	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986611	TTTTTAACATTTTAA[A/G]TTTAACAGATTGTAT	81929
rs569543645	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949747	CGTGAGCCACCGCGC[C/T]CGGCCCACGTTAACC	81929
rs569570776	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12964123	TCATTTCTTTTTAAC[G/T]GCTGCATAGAGCATG	81929
rs569592763	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12961233	ATAGATCAGTTAAGC[G/T]CCACCATTTTTCCTC	81929
rs569623446	snp	C/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12952305	TGGCGTGATCTTGGC[C/T]CACTGCAACCTCCGC	81929
rs569737012	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12984677	GAGGAAATAATAAAA[C/T]ACGAGATTGATTTTT	81929
rs569804308	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12980006	GGGCGCGGGGCTGAC[C/T]CCCCCACCTCCCTCC	81929
rs569839195	snp	A/G	0.000683223	0.0184701	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986862	TCTTCATTGTTTCAG[A/G]TATTTCTTTACCCCT	81929
rs569848196	snp	A/C	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12974022	CCATGCCTTAGCTGC[A/C]AGAGAGTGAGACAGC	81929
rs569850827	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12957547	CTGTTGAAGTTCCTC[A/G]TCTATAAAGTGAAAA	81929
rs569873287	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12954338	TTGGCCAACAGGAGG[G/T]GTGTAAGGATTTGGG	81929
rs569896770	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986339	CTATTCTAAGGCTTT[C/T]GCAGAAAAATAAGTG	81929
rs569927762	in-del	-/CT	0.00119737	0.0244387	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985783	TGATATTCAGTACAA[-/CT]CTGTCATTTCTTTGT	81929
rs570191171	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12980683	GACAGGGTGGCTGGC[A/C]GGGCGGGGGGCTGAC	81929
rs570315538	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12953182	TTGAGGTTCATCCAT[A/G]TTGTGTCATGTGTCA	81929
rs570340793	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947369	TTAGGCTGCCGAGCC[C/T]GGACTGCTTGTCATC	81929
rs570454173	snp	G/T	0.0023933	0.0345097	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946836	GACAGCTGGGACTAA[G/T]CATTTAAAAAACTTT	81929
rs570549327	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12960442	GCTATATATATGGAG[G/T]ATTGCATTCTGGGCT	81929
rs570577837	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12974557	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC	81929
rs570586867	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12959567	GCCAGTGCTCAAAAA[A/G]TTTTGGAGTTTGGAG	81929
rs570630931	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12968003	CAGTTTACAAGTGCA[C/G]AATCTCTAAATAGTG	81929
rs570680708	snp	C/T	0.00279162	0.0372561	intron-variant	SEH1L	GRCh38.p7	18:12980220	GGGGGGCTGACCCCC[C/T]CACCTCCCTCCCGGA	81929
rs570714005	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12980865	GGCGGCTGGCCGGGC[C/G]GGGGGCTGACCCCCC	81929
rs570759462	in-del	-/TTTTTTTTTTTT			intron-variant	SEH1L	GRCh38.p7	18:12958090	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTT]GAGACAGAGTCTTGT	81929
rs570772650	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954391	ACAATAGTCTGTTAT[C/T]GATAGACTGTATTGT	81929
rs570794325	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12950043	CTTTTTTCTTTTTCC[-/T]TTTTTTTTGAGGCAG	81929
rs570820431	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12972678	ACACCTTCTACCTTC[C/T]TAGATTGTTGGTGTC	81929
rs570837659	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968586	ACTGATGGTGATACG[G/T]ACTCTTTTTTCCTTT	81929
rs570874252	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12975220	TGGTCTCGAACTGTC[C/G]ACCTCAGGTGATCTG	81929
rs570881577	snp	A/C			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948055	GGTCTGGCTAGGCTA[A/C]GGGCCACGCGCCGCC	81929
rs570951316	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12963992	TGCTGGGATGACAGG[C/T]GTGAGCTGCTGCACC	81929
rs570984677	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948572	GTCGTGGGTCTTGCC[C/T]GCGCTGTTCACCCGA	81929
rs570988392	snp	A/G	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12971419	CAGGCATGAGTGATA[A/G]AGAGGAGAAAGTAGA	81929
rs571026987	snp	A/C	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12970847	TTACTAAGACCTCTT[A/C]AGTATCTTTTAAAAA	81929
rs571125575	snp	C/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12953859	CTATATCTTTAAAGG[C/T]TTTTTATTAACAGCC	81929
rs571132777	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12966249	AGGCATGTGCCACCA[C/T]GCCCGTCTAATTTTA	81929
rs571271270	in-del	-/CT	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12983936	AATGTAGCTCATAGC[-/CT]CTGTCTCGTTTCTTT	81929
rs571336766	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12977776	TTCAAATACTTAGGC[A/T]ATGTGTTACTCTTTT	81929
rs571415455	snp	A/G	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12950845	TTTGTTTTGAGATGG[A/G]GTCTTGCCATGTTGC	81929
rs571436488	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985464	ACACTATTTGAAACT[C/T]TTGAAATATAAACGG	81929
rs571533022	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12981935	CTTGATCTTGGCTCA[C/T]TGCAACCTCCACCTC	81929
rs571544911	in-del	-/G	0.0111196	0.0737302	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947714	AGGGCATGACGGGCC[-/G]GGGGCGGGACGAGGA	81929
rs571751644	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12950979	GGTGTGCACCACCAT[A/G]CCTGGTTTCAATATT	81929
rs571825190	snp	G/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955990	GGCATGAGCCACTGT[G/T]CCTAACTCTAAAATT	81929
rs571909916	snp	C/T	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12966749	AATAAATGTTATTGT[C/T]TCAAATTGGGGATAT	81929
rs571910014	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12957897	TTTATTTTGTAGAGA[C/T]GGGGTTTCACCATGT	81929
rs571922662	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985633	TTGGAAAATATAGAC[A/C]TATTTCTTTTGCTTT	81929
rs571925677	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12973118	GAGACTGAGGTGGGA[A/T]GATCACCTGAGCCTG	81929
rs572055899	snp	A/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12984760	TGTCATCTAGAGTCT[A/G]TTTCCATGTTCAAAT	81929
rs572126813	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12968710	CTGTACGATAATATT[C/G]TTTCATCATTTCAGT	81929
rs572456208	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12973949	AAAAAACACCTTTCC[C/T]AGAAGTATCTTAGCA	81929
rs572479712	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12950936	AGTAATCCCTCCTGC[C/T]TCAGCCTCTTGAGTA	81929
rs572511558	snp	C/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949108	TCGTGATCCACCCGC[C/T]TCGGCGCCTCGGCCT	81929
rs572643810	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946242	TCCATGTCATTATAT[A/G]TTTGCCAAAACCCAC	81929
rs572669327	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12964513	ATGACTAGATAGATA[C/T]CTTATTTGTGGTGAT	81929
rs572760194	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952119	TTCTAACATAATTAT[C/T]TTAGTAATTCAGAAT	81929
rs572795383	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951652	TGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA	81929
rs572880333	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12975403	TGAAGGAGCTTACAG[C/T]GCCTAGGATATGGAT	81929
rs572921569	snp	A/C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968220	TGTTAACAACTTACT[A/C/G]TCTCAACTAGGGAGG	81929
rs572994127	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949021	CCCCCGGCTAATCTT[C/T]TTTTTTTTTTGTATT	81929
rs573044326	snp	G/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12954707	CCCTGGGCTCAAGCA[G/T]TCTGCCCACCTCAGC	81929
rs573073162	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948433	CGCGGGCCGCCCTCC[C/T]GTGCGCCTGCGCAGC	81929
rs573128672	snp	A/G	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12976747	AGGTGGGCAGATCAC[A/G]AGGTCAGAAGATCGA	81929
rs573168396	in-del	-/T	0.0482946	0.147699	intron-variant	SEH1L	GRCh38.p7	18:12950018	TTTCACTTAGTATAA[-/T]TTTTTTTTTCTTTTT	81929
rs573191511	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954190	ATGTTAGCTATACAG[C/T]GTGAAACACATTTTC	81929
rs573196536	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12962612	AGCTGGGGCCACAGG[C/G]GTGCACCACCACACC	81929
rs573340438	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12963512	CCATTTTTCACCCAG[C/G]CATGTCATTTGTCCC	81929
rs573360501	snp	C/T	0.000430093	0.0146582	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12951899	GCATTGTACTGCTAG[C/T]TGGAAGGTTAGTATT	81929
rs573374276	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12965300	TACAGGCATGAGCCA[C/T]CTCGCCCAGTCCATT	81929
rs573473059	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970936	AGAATATGCTAAAAA[C/T]AGTTCATAAGGATGG	81929
rs573493501	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12970421	CATCTGTTTTTTCTT[C/T]TTCTTTTCTTTTTTT	81929
rs573587319	snp	C/G	0.021333	0.101051	intron-variant	SEH1L	GRCh38.p7	18:12981193	GATGGGATGGCGGCC[C/G]GGCAGAGACGCTCCT	81929
rs573640088	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954764	TGAGCCACTATGCCT[A/G]GTTGAATCAAATGAA	81929
rs573685587	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12969628	AGGAGATGGAGGTTG[C/T]AGTAAACCAAGATCA	81929
rs573746073	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12958809	ACTGCTACTATGAGC[A/G]TTGTTGTACAGATAA	81929
rs573966780	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949484	TTGAGACGGAGTCTT[A/G]CTCTGTCACCCAGGC	81929
rs574004396	snp	G/T	0.212728	0.247206	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949030	AATCTTTTTTTTTTT[G/T]TGTATTTTTTAGTAG	81929
rs574023245	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12969580	GTAATCCCAGCCACT[C/T]GGGAGGCCGAGGCAC	81929
rs574054609	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971060	GACAGGCTAACTGTA[A/G]GCTGGTTGTCTGCTT	81929
rs574123155	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12983966	TTAATTGTAGTTTAA[A/G]GACATGGGTACAGAT	81929
rs574191265	snp	C/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948853	AATTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTG	81929
rs574232085	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976817	AAAAATACAAAAAAA[A/C]CAAAAAACATTGGCC	81929
rs574250166	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12956226	ATTTTTTGCATTTTT[A/G]GTAGAGACGGGGTTT	81929
rs574255398	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12954528	CTGGAGTGCAGTGGC[A/G]CAATCTTGGCTTACT	81929
rs574274153	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12964315	CAGACTTTAATTCTG[C/G]TAGTCACTAGTATAT	81929
rs574341416	in-del	-/TC			intron-variant	SEH1L	GRCh38.p7	18:12978442	GCTGCCTCCTCTCTG[-/TC]TCTGCGTTTCTTCTC	81929
rs574384139	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12963571	TTGTAAATATTTTCA[C/T]GTGAACCTTTTGGAT	81929
rs574418260	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971576	GAGGCGGAGGTTGCA[A/G]TGAGCTGAGATTGCG	81929
rs574451313	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12976672	CATGGGTGTAGAAAC[A/C]ATGCATATTCTGGCC	81929
rs574453633	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946965	CTTTCGCTCCCCTGA[C/G]GCAAGCTTCCACTGT	81929
rs574495378	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12980380	GGGGGGCTGACCCCC[C/T]CACCTCCCTCCCGGA	81929
rs574504556	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12959907	TCACCGGTACTTGGA[A/G]ATAGAGAAAGGTTTA	81929
rs574535865	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948296	GAGTGGGTGGGCGGC[A/G]CGGGGAACGGGGCTG	81929
rs574662264	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12976117	ACAGATTCGGTATTT[C/T]AATGTCTGTGGGTCA	81929
rs574671898	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12959007	AAATCTTCATCAGCA[C/T]TTGTTGTGGTGCTAT	81929
rs574708732	snp	C/G	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12967610	TGCTCTGCACCTGCC[C/G]ATGAATGACCATGAA	81929
rs574839822	snp	C/G	0.00199481	0.0315187	intron-variant	SEH1L	GRCh38.p7	18:12981400	TCACGCCACTGCACT[C/G]CAGCCTGGGCACCAT	81929
rs574900493	in-del	-/A	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12954080	GGACAAAACAAGGTT[-/A]AAAAAAAAGGGTGCA	81929
rs574902386	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12970411	TTCCCCTGTCCATCT[G/T]TTTTTTCTTCTTCTT	81929
rs574945925	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12969097	TGCCTGTAATGCTAG[A/C]TACTCAGGAGGCTGA	81929
rs575264546	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12968101	CCACTTGTTTTTCTT[C/G]GGTGTCTGCTGATCT	81929
rs575274184	snp	C/T	0.0023933	0.0345097	intron-variant	SEH1L	GRCh38.p7	18:12980996	AGACGGGGTGGCTGC[C/T]GGGCGGAGGGGCTCC	81929
rs575306434	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12954052	AAGAATTAAAGATGA[C/T]ACAGAAAAGACTGGA	81929
rs575320213	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948874	TTTTTTTTTGAGACC[A/G]AGTCTCACTCTGTCA	81929
rs575357848	snp	C/T	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948385	CTGAGCGGAAGCCCT[C/T]CCCGCCCGCGTATTG	81929
rs575439677	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12974253	AGTGGACTATGTAGT[A/T]TCGTTATTAATACCT	81929
rs575469340	snp	G/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986550	AGATTAGAAAATGTT[G/T]TGAATTTATAAAATT	81929
rs575562572	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12962780	GCCCAACTCATTTAC[A/T]GTTAAAGGGTCTAAT	81929
rs575599511	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12981451	CTCCGTCTGCCATCC[C/T]GGCACCTCGGGAGGC	81929
rs575632154	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12977409	TGAAATAGCCTTTGC[A/C]TAGTTTCCTTTTATT	81929
rs575755391	snp	G/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12951056	GATTCTGTATTTTTT[G/T]AATTTGTCTACTCTG	81929
rs575804820	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12973409	AGTTCAAGTGATTCT[C/G]CTGCCTTAGCCTCCT	81929
rs575804867	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12965553	TGACTCCATGCTTAA[C/T]TGATAGTTTGGCTAG	81929
rs575841557	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12972620	TTACTCCCGTGGGCT[C/T]TGCAATTCCAAATGT	81929
rs575953972	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12984893	CTGTGGTTATATCCT[C/G]TTGTTATCCTATATA	81929
rs576165433	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12979182	AAACAAGTGAACAAA[A/G]GTCTCTGGTTTTCCT	81929
rs576189686	in-del	-/TCTTTTTTTT	0.00636936	0.0560724	intron-variant	SEH1L	GRCh38.p7	18:12974284	GTTTATCTTTTTCTC[-/TCTTTTTTTT]TCTTTGAGATGGAGT	81929
rs576318177	snp	C/T	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12958718	ATATTCCATTGTGTG[C/T]GTATACCACATTTTG	81929
rs576347268	snp	A/C	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12952200	TTTCTCTTAAAAAAA[A/C]AAAACAAAACCTTTA	81929
rs576426642	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12958779	GGTTGTTTCTACTTC[A/G]TGGCTATTGTGAATA	81929
rs576548493	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12980596	TCCCTCCCGGACGGG[A/G]CAGCTGGCCGGGCAG	81929
rs576574805	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12971377	TTTACTATAATATAC[C/T]AAGTTCTGTGCTAGG	81929
rs576585084	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987339	TCAAAGTGCCTGTTC[C/T]GTAAATTTTATTTTA	81929
rs576585747	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12967517	TGTGTAAAGGACATT[C/T]GTTTACCAATGACAG	81929
rs576585772	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12958175	TGCATTCTCCGCCTC[C/T]GGGGTTCAAGCGATT	81929
rs576619247	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12970565	GCTGAGACAAACGGC[A/T]CATGCCACCACACCA	81929
rs576735881	snp	C/G	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12979305	CAAGCATCTGTTTAA[C/G]AAAGCACATCTTGCA	81929
rs576832575	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946322	GATAATGATGTGTCA[A/G]TGTAGGTTCACTGAT	81929
rs576909868	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986428	CCCAGTATCATGTAC[A/G]CACTAAAAAAAATGT	81929
rs576986578	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12981337	AATCTCGGCACTTTG[C/G]GGGGCCAAGGCAGGC	81929
rs577050761	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985839	GAGTGAATTAATAAA[C/G]TAGTAATAGTAAAAT	81929
rs577206308	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12953301	TGTTTTTGGCTGTTA[C/T]GAGTAATGTTAAGAA	81929
rs577248317	snp	C/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12952789	CTCTTCTTTTCTTTT[C/T]TTTTTTTTTTGAGCT	81929
rs577417757	snp	C/T	1.64827e-05	0.00287073	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984071	TTGGAAGTGTACTGG[C/T]ATTTTGAAAGGTAAT	81929
rs577469497	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947539	CTTAAATGATTCAGG[A/G]CCGAGGACCGTGAGA	81929
rs577500900	snp	A/G	0.00119737	0.0244387	intron-variant	SEH1L	GRCh38.p7	18:12959358	ACCAGTTAAGCATTC[A/G]CCTACTTATTTATTT	81929
rs577606706	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955917	TTTAAAGTATTCTGG[C/T]TCACTGCAGTCTCAA	81929
rs577607587	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12975315	TAATTACAATATATA[A/G]CTTGCCTCAGGTAAG	81929
rs577642602	snp	A/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12955332	CAGTTTTCTTCTCTC[A/G]TAGAAGTAAAACTAT	81929
rs577825435	snp	C/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985358	CCGTTTGACCTCTCC[C/T]AAGATACACCAGCAG	81929
rs577871046	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12977157	TTGAGGTGTGTACCA[C/G]CTTGGTAGAGATTTT	81929
rs577908629	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947587	CATCTTTCTTCATTT[A/G]CACAGTATACCAATA	81929
rs578001352	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12964578	ATAATTTCAAATAAT[A/G]TATATATCTCTACAC	81929
rs578034795	snp	A/T	0.000798403	0.0199641	intron-variant	SEH1L	GRCh38.p7	18:12964382	TGTTATCTTTTTTTT[A/T]AAAATTTTTATTCTG	81929
rs578044346	snp	A/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12971679	CTCCCAGTATGATGT[A/T]CCATCTTGCAGTGAA	81929
rs578095449	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947556	CGAGGACCGTGAGAG[A/G]CAGTCTTCACTTTTT	81929
rs578153523	snp	C/T	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12951632	CTGACCTCAGGTGAT[C/T]CGTTTGCCTTGGCCT	81929
rs578171055	snp	C/T	0.00159617	0.0282053	intron-variant	SEH1L	GRCh38.p7	18:12951100	CCCCAAAAGTCACAC[C/T]GGTTTTGCAGTCATT	81929
rs578213824	in-del	-/A	0.00517822	0.0506191	intron-variant	SEH1L	GRCh38.p7	18:12976801	AACCCTGTCTCTACT[-/A]AAAAATACAAAAAAA	81929
rs578253429	snp	C/G	0.000399281	0.0141238	intron-variant	SEH1L	GRCh38.p7	18:12957053	AGCCTGGGCGACGGA[C/G]CGAGACTTGTCTCAA	81929
rs578253478	snp	A/G	0.0023933	0.0345097	intron-variant	SEH1L	GRCh38.p7	18:12965264	TGATCCGCCCACCTC[A/G]GCCTCCCAAACTGCT	81929
rs745333983	snp	A/G			intron-variant, nc-transcript-variant	SEH1L	GRCh38.p7	18:12975762	CAGCTGTGTGGACTG[A/G]GAGCAGGAACTCAGG	81929
rs745457974	in-del	-/G			intron-variant	SEH1L	GRCh38.p7	18:12984612	AGGCTTTCTAGAAGA[-/G]GGTACATTAAGTTAT	81929
rs745489007	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963219	TGTGAAGTTTGCTCC[C/T]AAGCACATGGGTCTT	81929
rs745513725	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12954522	CCCAGGCTGGAGTGC[A/G]GTGGCACAATCTTGG	81929
rs745603292	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12963749	ACAGAGTATTGCTCA[C/T]TTGCCCAGGCTGGAG	81929
rs745776891	snp	A/G	1.64871e-05	0.00287111	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982549	TCTGGTGGGCCAACA[A/G]AGTTTGAAATCCATA	81929
rs745846105	snp	A/G	1.65037e-05	0.00287256	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978884	AATTTTTACATTAAA[A/G]CCTGTGAGGTGAGTT	81929
rs745867864	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959418	AACTCCTGGGTTCAA[A/G]CGATCCTCCACCTTG	81929
rs745869856	snp	G/T	1.71755e-05	0.00293044	intron-variant	SEH1L	GRCh38.p7	18:12978703	AGTGATGTGTGGATT[G/T]TTGCACATTTTATTT	81929
rs746088451	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959058	ACTGTGTTGTGAAGT[A/G]GCATCTCCATTGTGG	81929
rs746259882	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12968680	TCTAATGGCACTCTT[C/T]CTAGATTTCTAGCCC	81929
rs746261315	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12965234	AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTTGT	81929
rs746277787	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12953493	ATCCTCACCTACACT[C/T]GATAATATCTGTCTT	81929
rs746291412	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12952232	CAAGTAGAAATTTTC[-/T]TTTTTTTTTTTTTTT	81929
rs746349744	snp	A/G	4.94417e-05	0.00497176	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984144	CCTTCCCTAGGTTCA[A/G]CTATTCCAAGTCTTC	81929
rs746354672	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947142	ACTTCCTTTTCCCCG[A/G]AGGACTCTGGCTCCC	81929
rs746384745	snp	C/T	0.001306	0.0255205	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948073	GCCACGCGCCGCCGC[C/T]GCTGCCGCCGCCACT	81929
rs746576734	in-del	-/ACCCGCCCCC			intron-variant	SEH1L	GRCh38.p7	18:12969207	AGAGCAAAACTCTGT[-/ACCCGCCCCC]CCCCCCCCCCCCACC	81929
rs746577623	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12974176	GGAGTTCTGTTGCTG[A/G]TTCTTTGAGGTAAGC	81929
rs746615642	snp	C/G	1.64746e-05	0.00287002	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955528	GCAGGTTTTGGCTTC[C/G]TGTTCTTTTGACCGA	81929
rs746645650	snp	A/G	3.44406e-05	0.00414959	intron-variant	SEH1L	GRCh38.p7	18:12984258	GTAGCCATACTTAAG[A/G]TGGATTATTTCATGG	81929
rs746658258	in-del	-/TTT	0.000878986	0.0209457	intron-variant	SEH1L	GRCh38.p7	18:12955441	GTATCTGTTCTTTTC[-/TTT]TTTTTTTTTGATTCC	81929
rs746698872	snp	A/G	1.64792e-05	0.00287042	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984125	TCAGCAGGGAACCTC[A/G]AATCCTTCCCTAGGT	81929
rs746757592	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976439	AGGTGCGGGTCATGG[A/G]GGCACTTAGAATCTC	81929
rs747016005	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12972061	GGGATCAGATGGATC[C/T]TCTATAGGTGTGACA	81929
rs747016438	snp	A/C	8.24681e-05	0.00642085	intron-variant	SEH1L	GRCh38.p7	18:12971135	GTTATCTAAAATGTT[A/C]TTTCTCCCCGTTTCT	81929
rs747084587	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12976315	TGTGTTGTAGTCACA[C/T]GGGTGTTGTCCCACC	81929
rs747103951	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12958994	TTCCAGTTTTTCCAA[A/G]TCTTCATCAGCACTT	81929
rs747244492	snp	C/T	1.65176e-05	0.00287376	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987001	CAGTATCCTCACCCT[C/T]GCAGACGATATCTCT	81929
rs747268929	snp	A/G	8.39877e-05	0.00647972	intron-variant	SEH1L	GRCh38.p7	18:12951924	AGTATTTATTTTTAC[A/G]TTTATTAAAAATACA	81929
rs747323548	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12978459	TCTGCGTTTCTTCTC[C/T]TCTTTTTAAAGAATA	81929
rs747343010	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12959467	ATTACAGGTGTGAGC[C/T]ACCGTGGCCAGCCCC	81929
rs747343686	in-del	-/GTTTG	8.87981e-05	0.00666267	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986827	TCCTGTTTTTGTTTT[-/GTTTG]GTTTGGTGTTTTGTT	81929
rs747371596	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12982025	CCACCATGCCTGGCT[A/G]ATTTTTTATTTTGTA	81929
rs747537985	snp	A/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971199	GGAAGTGATGACAGT[A/G]GCCCCAACGCAATGG	81929
rs747547449	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12951132	GTGCATGTGTGAGGA[C/G]TGGTGAAAAAGTTTG	81929
rs747547667	snp	A/G	1.66236e-05	0.00288297	intron-variant	SEH1L	GRCh38.p7	18:12955416	GAAAAAAGAAGCCCT[A/G]GGATAATGAGTATCT	81929
rs747624219	snp	A/G	1.64784e-05	0.00287035	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984106	GCCCAGTCAATGGGA[A/G]TTCTCAGCAGGGAAC	81929
rs747626854	in-del	-/G	1.64743e-05	0.00287	frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955511	GCCCATCCTGAATTT[-/G]GGCAGGTTTTGGCTT	81929
rs747689273	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12965370	AATATTTACATTCTG[G/T]AAACATTTAACACAT	81929
rs747754353	snp	A/G			utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987211	GTGTTTGGAACCTAA[A/G]TCTGTTTGTGCGTCT	81929
rs747782998	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12954551	GCTTACTGCAGCCTC[-/A]AACCTTCCAGGCTGA	81929
rs747804822	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12967329	ACAACACAAACTACT[C/T]AGACCTGAATAAAGC	81929
rs747910187	in-del	-/TCT			intron-variant	SEH1L	GRCh38.p7	18:12978457	TCTCTGCGTTTCTTC[-/TCT]TCTTTTTAAAGAATA	81929
rs748143508	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955517	CCTGAATTTGGGCAG[A/G]TTTTGGCTTCCTGTT	81929
rs748275777	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12970449	TTTCTGAAAGAGACT[C/T]TCACTCTGTTGCCCA	81929
rs748319733	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12974060	TGGCATTTTCAGCAT[C/T]AAAAACGAGGGGAAG	81929
rs748334053	snp	G/T	0.000115717	0.00760559	intron-variant	SEH1L	GRCh38.p7	18:12951814	TTGTATCAATTTGTA[G/T]GAATTTTTGTATAAA	81929
rs748389019	snp	C/G/T	5.22237e-05	0.00510975	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948190	CTCTTTCGACTTCCA[C/G/T]GGGCGGCGGATGGCA	81929
rs748405268	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12983970	TTGTAGTTTAAGGAC[A/G]TGGGTACAGATTTGT	81929
rs748469825	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12958867	TTGGAAATATACCTA[C/G]GAGTAGAATTGCTGG	81929
rs748558951	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12977746	CCTGTTACCAGCTTT[A/G]CTTTTTTATTTACAT	81929
rs748589435	in-del	-/CTATTGCCCAGGCTGGAGT			intron-variant	SEH1L	GRCh38.p7	18:12964669	AGATGGAGTCTTGCC[-/CTATTGCCCAGGCTGGAGT]CTATTGCCCAGGCTG	81929
rs748647720	snp	G/T	1.65165e-05	0.00287367	intron-variant	SEH1L	GRCh38.p7	18:12971126	ATTTCTTTTGTTATC[G/T]AAAATGTTCTTTCTC	81929
rs748692771	snp	A/C	1.65116e-05	0.00287324	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986983	GCTGACACTGCCAAC[A/C]TCCAGTATCCTCACC	81929
rs748749901	snp	C/G	1.64787e-05	0.00287038	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982567	TTTGAAATCCATATA[C/G]TGGCTCAGTTCGATA	81929
rs748760174	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12962742	CTTCCCAAAGTTTTG[A/G]GATTACAGGTGTAAG	81929
rs748785252	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12977582	ATACAAAATTAGCCA[C/G]GCGTAGTGGTGCACG	81929
rs748829516	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12951288	TTTGCTGTTTAAAAT[C/G]GCCTCCAAGCGTAGT	81929
rs748918847	snp	C/T	1.65649e-05	0.00287788	intron-variant	SEH1L	GRCh38.p7	18:12963413	AACATCCTAGTAAAA[C/T]AAACTAGTAACTTTT	81929
rs748986076	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12963533	CATTTGTCCCTGTTT[G/T]CACTCAACAGAGGAA	81929
rs749019636	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12957428	GCGAGACTTCGTCTC[-/A]AAAAAAAAAAAAATA	81929
rs749043100	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986832	GTTTTTGTTTTGTTT[A/G]GTGTTTTGTTCCTGT	81929
rs749115334	snp	C/T			missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971169	TCTCGTGCTCATTCC[C/T]CCATGATCGCCGTAG	81929
rs749132093	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12972393	TAGAGTGTGGCAGCA[C/T]GTGAAGGTAAGTTAA	81929
rs749216407	snp	A/C	3.33056e-05	0.00408065	intron-variant	SEH1L	GRCh38.p7	18:12955412	TTAGGAAAAAAGAAG[A/C]CCTGGGATAATGAGT	81929
rs749267810	snp	G/T	3.32873e-05	0.00407953	intron-variant	SEH1L	GRCh38.p7	18:12982694	AGAGTTCAGTGAAGG[G/T]GTAATTGTTGGTTTA	81929
rs749269892	snp	C/T	1.65222e-05	0.00287417	intron-variant	SEH1L	GRCh38.p7	18:12951852	CCTTTTATTTTCTTA[C/T]AGGTCTGGGATAAAA	81929
rs749359335	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12957132	TTTGTTTTCTTAGGA[A/G]ATATACTGTCCTCGG	81929
rs749429704	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12983790	ATTGTCTTTGCTAGT[A/T]TCTGTAAGATGGGTG	81929
rs749493338	snp	A/G	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978830	TCCAAATTTGGGAAG[A/G]TCTTTCCATATTCTA	81929
rs749504403	snp	A/C	2.50423e-05	0.00353843	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948082	CGCCGCCGCTGCCGC[A/C]GCCACTGTCCTCTTC	81929
rs749509680	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946509	GTTTCACCTAATTCA[A/G]CACTTCACTCCCACT	81929
rs749546370	snp	C/T	1.70435e-05	0.00291915	intron-variant	SEH1L	GRCh38.p7	18:12978720	TGCACATTTTATTTC[C/T]AAAATGTTAATGTCA	81929
rs749602230	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963241	ATGGGTCTTATGTTA[A/G]CAACCTGTTCCGCAG	81929
rs749618150	in-del	-/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946636	ATATTTTGATTGGAC[-/T]TTTTATAGTGAGCAC	81929
rs749787395	snp	C/T	2.15827e-05	0.00328494	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986878	TATTTCTTTACCCCT[C/T]TGGATTCCCCACGGG	81929
rs749859772	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12981934	GCTTGATCTTGGCTC[A/G]CTGCAACCTCCACCT	81929
rs750003792	snp	A/T	3.2962e-05	0.00405954	missense, stop-gained, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963370	TCTTGGAACCCTTCA[A/T]GGTAAGTTTACATAT	81929
rs750077121	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12969990	TATTATAAATAACTT[A/C]TAATTTTATTTTATT	81929
rs750078379	in-del	-/CCCTCCCTCTC			intron-variant	SEH1L	GRCh38.p7	18:12952741	TTCTTCTCTCCTCTG[-/CCCTCCCTCTC]CCCTCCCCTCCCACC	81929
rs750166344	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12950903	GGGCGTGATCATAGC[C/T]TTAAACTCCTGGGCT	81929
rs750184937	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12978165	TTTATTAAAGCGTTT[C/T]GAGCTAAATGTACAT	81929
rs750277308	in-del	-/TTTTCT	1.70321e-05	0.00291818	intron-variant	SEH1L	GRCh38.p7	18:12955436	AATGAGTATCTGTTC[-/TTTTCT]TTTTTTTTTTTGATT	81929
rs750311557	snp	G/T	4.98012e-05	0.0049898	intron-variant	SEH1L	GRCh38.p7	18:12982687	AAAGGTAAGAGTTCA[G/T]TGAAGGGGTAATTGT	81929
rs750335306	in-del	-/AATGTTCTTTCT	1.65111e-05	0.0028732	intron-variant	SEH1L	GRCh38.p7	18:12971129	TCTTTTGTTATCTAA[-/AATGTTCTTTCT]CCCCGTTTCTAGCTC	81929
rs750446094	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12974988	CCTTAATTATTTTTA[C/T]TTTTATTTTATTTTT	81929
rs750531439	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12976165	GGAAAGACTCCACTT[C/T]GGAGCTCACCTGGTT	81929
rs750548098	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12960499	TCCTTGTCCTAATAG[C/T]ACACTGTTTTAATTC	81929
rs750691521	snp	A/G	4.95356e-05	0.00497648	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955593	CAAATGATAAACTGC[A/G]AGGACAGAGCCACTG	81929
rs750811970	snp	A/G	1.91049e-05	0.00309065	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948257	GCGCTTGCGGGCGGG[A/G]CCGACCCCGGAAGGA	81929
rs750836925	in-del	-/AG			downstream-variant-500B	SEH1L	GRCh38.p7	18:12988011	CCTCTTATCAGGGCT[-/AG]AGAGAGAGGTGTTTT	81929
rs750866804	snp	G/T	4.97929e-05	0.00498939	intron-variant	SEH1L	GRCh38.p7	18:12978914	TTTAGAAGCATTTAT[G/T]AATTTGAAAATACTC	81929
rs750906891	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12961334	CAGGTGTTTCTATCT[G/T]TTGGGAGACTACCTT	81929
rs750911370	snp	A/G	5.7038e-05	0.00534001	missense, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948138	TGTTTGTGGCTCGCA[A/G]CATCGCGGCGGACCA	81929
rs750949514	snp	C/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947642	GTAACTCGCCTTTTG[C/G]AGAGCACCCTCCGCC	81929
rs751087478	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12954370	TTCCCCATATTTGCT[C/T]TTCCTACAATAGTCT	81929
rs751138515	snp	C/G	6.93666e-05	0.00588884	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985302	TGCTTGTTGCATGCA[C/G]ACAGGAATGGAAAGC	81929
rs751217794	snp	C/T	1.87373e-05	0.00306077	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948249	TGCGCGCGGCGCTTG[C/T]GGGCGGGGCCGACCC	81929
rs751261388	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12972812	GAGCCCTATTAATAG[A/C]ACATTTTATAGAGGC	81929
rs751330984	in-del	-/A	0.000194775	0.00986658	intron-variant	SEH1L	GRCh38.p7	18:12971303	TGCATTTAATTTTTT[-/A]AAATGTTATTTCTTT	81929
rs751444271	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12977154	ACCTTGAGGTGTGTA[A/C]CAGCTTGGTAGAGAT	81929
rs751457465	snp	C/T	6.58903e-05	0.00573941	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963342	CTCATGTAAGCTAAG[C/T]TGTAGTTGTATTTCT	81929
rs751464274	snp	A/G	1.64825e-05	0.00287071	missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963169	TTTTAGGTTAAAAGG[A/G]CAACTCTGGTGGATA	81929
rs751679216	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12966576	GCTAATTTTTTGTTA[-/T]TTTTTTGTGGATATG	81929
rs751698148	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12951444	CTCCCAGGCTGGAGT[A/G]CAGTGGCGTGATGTC	81929
rs751701839	snp	C/T	1.64751e-05	0.00287007	intron-variant	SEH1L	GRCh38.p7	18:12955455	CTTTTTTTTTTTTGA[C/T]TCCCCAGACACATAG	81929
rs751719831	snp	A/G	3.29821e-05	0.00406078	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955581	TAGTAGGAGAATCAA[A/G]TGATAAACTGCGAGG	81929
rs751806279	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12960280	GAGTGGTTAACATGC[A/G]CAAGCAAGCAAGGGC	81929
rs751865021	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12952687	TATTCCCACTCCAAG[A/C]CCCAGGCAACCACTG	81929
rs751974219	in-del	-/TTTTTTTTTT			intron-variant	SEH1L	GRCh38.p7	18:12958076	TTAACTTTTTTTTTT[-/TTTTTTTTTT]TTTTTTTTTTTTTTT	81929
rs751977396	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12961197	GGCGTTTTTCCCTTA[A/C]CAGAATGTTCCTAGA	81929
rs751985405	in-del	-/C			intron-variant	SEH1L	GRCh38.p7	18:12974389	GGTTCAAGCGATTCT[-/C]CTGCCTCAGCCTCCC	81929
rs752099519	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12959382	TTTATTTACTTAATA[G/T]AGTTGCCCAGGCTGG	81929
rs752178578	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12966915	TCTCCACTTTGTTCT[C/T]CAGGTATACATTTTT	81929
rs752189420	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12957713	AACAAAAGGAAGTGT[A/G]TAGTGGGAGTGTCCT	81929
rs752197144	snp	A/G	0.00016001	0.00894311	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948112	CGGAGGCGCGGGCCC[A/G]ACGGAAACCATGTTT	81929
rs752263431	in-del	-/TTTG	3.87064e-05	0.00439906	intron-variant	SEH1L	GRCh38.p7	18:12982479	TATATGTTTTAAAAC[-/TTTG]TTTGGAATGCCTCAG	81929
rs752346301	snp	C/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946853	ATTTAAAAAACTTTC[C/T]AGCCTGCTAATTTTA	81929
rs752462732	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12956049	AGGGTTAATAAAATT[C/T]TTTTTTTTTTTTTTA	81929
rs752548941	snp	A/G	1.66026e-05	0.00288115	intron-variant	SEH1L	GRCh38.p7	18:12955617	GCCACTGGGTGAGAC[A/G]TTTATTAGTATTCTG	81929
rs752595545	snp	A/G	8.52929e-05	0.00652987	intron-variant	SEH1L	GRCh38.p7	18:12984245	TTAAATCATTCTGGT[A/G]GCCATACTTAAGGTG	81929
rs752653247	snp	C/T	1.65468e-05	0.00287631	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985293	CTGTTTTGCTGCTTG[C/T]TGCATGCACACAGGA	81929
rs752653547	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12968448	CTTACCTTTTCTTTT[C/T]CAAGTTCTAATTGTC	81929
rs752713059	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12950812	CTATATTTTTTCTGG[A/G]TAATAAGGTTTAATT	81929
rs752757933	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12964549	TAGTTGTTGGAGTTA[C/T]ACTGGTAATTATTAT	81929
rs752770888	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12964586	AAATAATATATATAT[C/G]TCTACACATATTTAT	81929
rs752829682	snp	C/T	1.65836e-05	0.0028795	intron-variant	SEH1L	GRCh38.p7	18:12951908	TGCTAGCTGGAAGGT[C/T]AGTATTTATTTTTAC	81929
rs752834677	snp	G/T	3.29843e-05	0.00406092	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982656	TTCAGGAGATGATGG[G/T]TGTGTAAGATTGTGG	81929
rs752851520	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12951397	ATTCAAGGTTCTCAA[C/T]GTAAATTTTTTGAGA	81929
rs752853402	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12963551	CTCAACAGAGGAAGC[C/T]GGCATTGTAAATATT	81929
rs752934834	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12950657	AATTAGTGGATATTT[C/T]AAACACTATTGAAGA	81929
rs753040811	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12973232	AAGAAAATATTTCAT[A/G]AGTAAGATTTGAGTA	81929
rs753131224	in-del	-/ACCC			intron-variant	SEH1L	GRCh38.p7	18:12969207	AGAGCAAAACTCTGT[-/ACCC]GCCCCCCCCCCCCCC	81929
rs753139651	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12973674	GATTGCATTTGAGTC[-/T]AGTCTCTTAGCTAAC	81929
rs753147264	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959325	ATTTTGGATTTTGCA[A/G]TATTTGCATTTATAC	81929
rs753237063	snp	C/T	1.71223e-05	0.00292589	utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987074	ACACTGATTTAACAT[C/T]GAAAGGCCTTATTCA	81929
rs753340930	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12953024	TGACCTCAAGTGATC[C/T]GCCCGCCTTGGCCTT	81929
rs753351887	snp	C/T	1.64795e-05	0.00287045	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971237	TCAGATTTTTGAATA[C/T]AATGAAAACACCAGG	81929
rs753494958	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959278	TATTCCTTATCCATA[A/G]TGCTAGGATCCAGAA	81929
rs753499801	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12958551	TCTACCCCCTATTCA[A/G]CTGTCTGTCTATAAA	81929
rs753501548	snp	A/G	3.29478e-05	0.00405867	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971172	CGTGCTCATTCCCCC[A/G]TGATCGCCGTAGGAA	81929
rs753563802	snp	A/T	0.000151688	0.00870751	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987054	TGAGAATGAAGGGAT[A/T]TAAAACACTGATTTA	81929
rs753594962	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12955191	GTTTATCTGGCTAGA[-/T]TTTTCTTTTATTAGT	81929
rs753601099	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12966726	TGACACTCAGTGGTC[C/G]CTTTAAAAATAAATG	81929
rs753750638	snp	G/T	3.37268e-05	0.00410637	intron-variant	SEH1L	GRCh38.p7	18:12984230	GAAATCATCTTTGTT[G/T]TAAATCATTCTGGTA	81929
rs753754691	snp	A/G	3.29457e-05	0.00405854	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955492	TGTATGGCGTGTGAC[A/G]TGGGCCCATCCTGAA	81929
rs753867750	in-del	-/GTA			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949389	CAATTTTTAAAAGAT[-/GTA]GTTTCTTTTTTAAAA	81929
rs753884911	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976837	AAACATTGGCCGGGC[A/G]TGGTGGCAGGCCCCT	81929
rs753933659	snp	G/T			missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963308	TGAATCTCAGCCAGT[G/T]GTCTTTGCAGCATGA	81929
rs753954268	snp	G/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948763	ATCCAATGATTTCCC[G/T]GCTTGCTGCCCAGGA	81929
rs753970501	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12984277	ATTATTTCATGGATT[A/G]TAAGATGGAGTGGAA	81929
rs753992600	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976398	CACTCATGGGGAGGA[A/G]CCTCCACAAGGGCGG	81929
rs754080928	snp	C/T	6.60437e-05	0.00574608	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986979	CGATGCTGACACTGC[C/T]AACCTCCAGTATCCT	81929
rs754300260	snp	A/G	1.6537e-05	0.00287545	missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12951894	GATTGGCATTGTACT[A/G]CTAGCTGGAAGGTTA	81929
rs754359932	snp	C/T	1.64754e-05	0.00287009	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982622	TGAGTTGGAATATAA[C/T]AGGAACGGTGCTAGC	81929
rs754412757	snp	C/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948463	CTGGTGCCACGTGCG[C/T]GCTCCCGCCCGCAGG	81929
rs754486989	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12978243	CATAACAAATTACCA[C/G]AAATCAGGTGGCTTA	81929
rs754489384	in-del	-/G			intron-variant	SEH1L	GRCh38.p7	18:12985140	TTTCTTTTGTAAATA[-/G]CTTCTATTTTTTGAT	81929
rs754511627	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12981753	AAATTAGTATTGAGA[C/T]AGTCTTGTGAATAAC	81929
rs754578831	in-del	-/T/TT	0.0808932	0.184252	intron-variant	SEH1L	GRCh38.p7	18:12955440	GTATCTGTTCTTTTC[-/T/TT]TTTTTTTTTTTTGAT	81929
rs754582493	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12965507	ATGGAATGGATGGCA[A/G]ACTCTTCAAATACCT	81929
rs754638850	snp	C/T	4.94205e-05	0.0049707	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971177	TCATTCCCCCATGAT[C/T]GCCGTAGGAAGTGAT	81929
rs754666890	in-del	-/AATGTC	3.36474e-05	0.00410153	intron-variant	SEH1L	GRCh38.p7	18:12978729	TATTTCTAAAATGTT[-/AATGTC]AATTGTTTTTCCATT	81929
rs754676384	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959284	TTATCCATAATGCTA[A/G]GATCCAGAAATGTTT	81929
rs754730828	snp	A/T	1.69504e-05	0.00291117	intron-variant	SEH1L	GRCh38.p7	18:12984237	TCTTTGTTTTAAATC[A/T]TTCTGGTAGCCATAC	81929
rs754774049	snp	A/G	4.95511e-05	0.00497726	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955596	ATGATAAACTGCGAG[A/G]ACAGAGCCACTGGGT	81929
rs754829076	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955509	GGGCCCATCCTGAAT[C/T]TGGGCAGGTTTTGGC	81929
rs754882167	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12966860	TTTACTCTCCATTTA[A/C]AACAAAATTGTTTGG	81929
rs754894205	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12975212	GGTCAGGCTGGTCTC[A/G]AACTGTCGACCTCAG	81929
rs754968936	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12963390	AGTTTACATATTAAA[A/C]CTCTGATAACATCCT	81929
rs754998481	snp	A/T	1.64792e-05	0.00287042	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984101	TGGGAGCCCAGTCAA[A/T]GGGAGTTCTCAGCAG	81929
rs755005128	snp	A/C	4.1238e-05	0.00454063	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948282	GAAGGAAGGAAGGGG[A/C]GTGGGTGGGCGGCGC	81929
rs755060044	snp	A/G	1.86107e-05	0.00305041	intron-variant	SEH1L	GRCh38.p7	18:12982489	AAAACTTTGTTTGGA[A/G]TGCCTCAGAAAATGT	81929
rs755088099	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12961826	CGCCCGCCACAATGT[C/T]TGGCTAATTTGAATA	81929
rs755203361	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12961593	GTTTATGTAATATTA[C/T]CCTTTTAATGTTGAG	81929
rs755307523	snp	A/G			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948476	CGCGCTCCCGCCCGC[A/G]GGGTACGCCGGGCCC	81929
rs755349669	snp	A/G	1.68835e-05	0.00290542	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987056	AGAATGAAGGGATTT[A/G]AAACACTGATTTAAC	81929
rs755349793	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12957598	AAGACTCTTTCCAGC[A/G]TTTTCATATGAAGGT	81929
rs755361855	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12971748	AAGTGGAAGAATTAG[A/G]GTGCTAAAGAGCTTA	81929
rs755367431	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12958562	TTCAACTGTCTGTCT[A/G]TAAATTTGACTAGGT	81929
rs755440463	in-del	-/AAAA			intron-variant	SEH1L	GRCh38.p7	18:12967930	AAAGAGAAAAAAAAG[-/AAAA]AAAAAAAGAAAGCCT	81929
rs755484531	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12984303	GGAAATGTTCACATG[-/T]TGCTTGTATTAGCAT	81929
rs755515480	snp	A/C	1.65386e-05	0.00287559	missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12951895	ATTGGCATTGTACTG[A/C]TAGCTGGAAGGTTAG	81929
rs755615997	in-del	-/ATC	1.64747e-05	0.00287003	cds-indel, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982583	TGGCTCAGTTCGATA[-/ATC]ATAATTCTCAGGTCT	81929
rs755770612	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12964634	ATTTACTCCCGTCTC[-/T]TTTTTTTTTTTTTTT	81929
rs755815221	snp	C/T	7.14592e-05	0.005977	intron-variant	SEH1L	GRCh38.p7	18:12951944	TTAAAAATACAGAAA[C/T]ATTTACTGTTTATTT	81929
rs755822418	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963228	TGCTCCCAAGCACAT[A/G]GGTCTTATGTTAGCA	81929
rs755838036	in-del	-/TGGT			intron-variant	SEH1L	GRCh38.p7	18:12983175	AGTTGACACTGACTG[-/TGGT]CTCTGTAGCTTGGTT	81929
rs755942807	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12965269	CGCCCACCTCGGCCT[C/T]CCAAACTGCTGGGAT	81929
rs756049304	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12977413	ATAGCCTTTGCATAG[C/T]TTCCTTTTATTATCA	81929
rs756145911	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12963794	CTTGGCTCACAGTAG[A/C]CTCCACCTCCTGAGT	81929
rs756155707	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12960501	CTTGTCCTAATAGCA[A/C]ACTGTTTTAATTCCG	81929
rs756481671	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12968719	AATATTCTTTCATCA[C/T]TTCAGTGGGCTTTTG	81929
rs756482575	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12977196	TGTTGGGATGAAAAG[A/G]AGGTCAAGTGAAGAA	81929
rs756629446	snp	C/G	1.88025e-05	0.00306609	missense, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948143	GTGGCTCGCAGCATC[C/G]CGGCGGACCACAAGG	81929
rs756720630	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12983482	TCAGGACCACCTTGC[C/T]ATGCTCCCCAGCAGG	81929
rs756729957	snp	A/G/T			intron-variant	SEH1L	GRCh38.p7	18:12969909	AAACAGGAAAAAAAC[A/G/T]CAAAAGGAAGTTTGT	81929
rs756796713	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12983225	ATGATTATCCATTAG[A/G]CAGAGATGTCTGTGA	81929
rs756816860	snp	C/G			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948919	CAATGGCACGATCTC[C/G]GCTCACTGCAACGTC	81929
rs756859600	snp	A/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946412	GACAGTAGGGGTACA[A/T]ACGGGAACTCTATTT	81929
rs756960021	snp	G/T	1.64974e-05	0.00287201	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982542	GACTTCCTCTGGTGG[G/T]CCAACAAAGTTTGAA	81929
rs756964619	snp	A/G	3.44988e-05	0.0041531	intron-variant	SEH1L	GRCh38.p7	18:12984260	AGCCATACTTAAGGT[A/G]GATTATTTCATGGAT	81929
rs756984665	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12962029	AACTTTTAAATGTGA[C/T]GTTGGAATTTTACAG	81929
rs757060545	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12982982	TGCTCTACAAACTCA[A/G]GCTAGGACTGTAGTG	81929
rs757145910	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12963592	CCTTTTGGATGTTTT[C/T]TATGCATATGCAAAT	81929
rs757264868	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12973672	GAGATTGCATTTGAG[G/T]CTAGTCTCTTAGCTA	81929
rs757288322	in-del	-/TTTATT	0.000448084	0.0149613	intron-variant	SEH1L	GRCh38.p7	18:12951913	GCTGGAAGGTTAGTA[-/TTTATT]TTTACATTTATTAAA	81929
rs757294492	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976458	ACTTAGAATCTCTCT[A/G]CCACAGTACGGGTGT	81929
rs757337206	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12959386	TTTACTTAATAGAGT[A/T]GCCCAGGCTGGTCTT	81929
rs757447533	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12978070	TGGGTTCAAGCAATT[C/G]TCCCACCTCAGCCTC	81929
rs757548850	snp	C/T	0.0680428	0.17144	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955468	GATTCCCCAGACACA[C/T]AGTGGATCTGTATGG	81929
rs757604906	in-del	-/TT			downstream-variant-500B, utr-variant-3-prime	SEH1L	GRCh38.p7	18:12987554	TGGACTTTTTGGTCT[-/TT]TTTTTTTTTTTTTTT	81929
rs757616369	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12965193	AATTTTTTGTATTTT[C/T]AGTAGAGACGGGGTT	81929
rs757645712	snp	A/C			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947113	GCCTCTTCCCAGGGG[A/C]TCTGGCCCTCTTCAC	81929
rs757752688	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12971302	TTGCATTTAATTTTT[A/T]AAAATGTTATTTCTT	81929
rs757798049	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12960358	AAATCTAGTTTTCCC[A/G]GCACCATTTCTTGAA	81929
rs757842349	snp	C/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946025	GAGAAAGCTTAAATG[C/G]ATATTACTATAAGGA	81929
rs757855180	snp	C/T	3.29576e-05	0.00405928	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984107	CCCAGTCAATGGGAG[C/T]TCTCAGCAGGGAACC	81929
rs757868447	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12967169	GCTAATACTGAATAC[C/G]GAATTGCTCCTTGGG	81929
rs757890122	snp	C/T	1.71217e-05	0.00292584	intron-variant	SEH1L	GRCh38.p7	18:12984250	TCATTCTGGTAGCCA[C/T]ACTTAAGGTGGATTA	81929
rs757958089	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12968472	AATTGTCTCACTAAG[A/G]CAATGTTTTTTGACC	81929
rs757996732	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12953251	ATTGCCACGTTTTGT[C/T]TGTCTGTTCACCAGT	81929
rs758134553	snp	A/C			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946906	TCCTGGCCAAAATCC[A/C]AAGGGCAAGTCCCTT	81929
rs758261610	snp	G/T	1.71029e-05	0.00292424	intron-variant	SEH1L	GRCh38.p7	18:12963151	AAATTGTTATTATTT[G/T]TTTTTTAGGTTAAAA	81929
rs758276566	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12976400	CTCATGGGGAGGAGC[C/T]TCCACAAGGGCGGGA	81929
rs758297225	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12956195	GACTACAGGCGCCCG[C/T]CACCACGCCCATCTA	81929
rs758357726	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12951400	CAAGGTTCTCAATGT[A/G]AATTTTTTGAGACGG	81929
rs758405955	snp	A/G	1.66618e-05	0.00288628	intron-variant	SEH1L	GRCh38.p7	18:12955635	TATTAGTATTCTGGG[A/G]ACCGGGAAGACATGA	81929
rs758468908	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12964615	ATCAATTTTTAGACT[A/G]TATATTTACTCCCGT	81929
rs758593010	snp	C/T	1.65266e-05	0.00287455	intron-variant	SEH1L	GRCh38.p7	18:12951837	TGTATAAAATATCTG[C/T]CTTTTATTTTCTTAT	81929
rs758641230	snp	A/G	1.6588e-05	0.00287988	intron-variant	SEH1L	GRCh38.p7	18:12951910	CTAGCTGGAAGGTTA[A/G]TATTTATTTTTACAT	81929
rs758698474	snp	A/G	1.65053e-05	0.0028727	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982662	AGATGATGGGTGTGT[A/G]AGATTGTGGAAAGGT	81929
rs758784105	snp	A/G	1.67066e-05	0.00289016	intron-variant	SEH1L	GRCh38.p7	18:12971279	TTGGTTTTAATAATT[A/G]TTCAGAATTGCATTT	81929
rs758810300	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12959344	TTGCATTTATACTTA[C/G]CAGTTAAGCATTCGC	81929
rs758890127	snp	A/C	1.73276e-05	0.00294338	utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987090	GAAAGGCCTTATTCA[A/C]GTGCTTGTAAATGCT	81929
rs758908748	snp	C/G/T	4.94347e-05	0.00497145	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978785	AACTCTTATGACAGT[C/G/T]ACTGATCCTGTTCAT	81929
rs758970107	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12973373	GATGCAATCTCAGCT[C/G]ACTGCAACCTCTACC	81929
rs759023840	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12978688	AAAAAGGTGAGATGC[A/C]GTGATGTGTGGATTT	81929
rs759114145	snp	A/T	1.7714e-05	0.00297602	intron-variant	SEH1L	GRCh38.p7	18:12984288	GATTATAAGATGGAG[A/T]GGAAATGTTCACATG	81929
rs759169432	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12961093	TTCTTCCCTTGGGGT[G/T]GGCAGTCCGCATGTG	81929
rs759182478	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12957511	TTTGAATTTGGGCAA[A/G]AACATAATATAATCT	81929
rs759270538	in-del	-/TTTAG			intron-variant	SEH1L	GRCh38.p7	18:12960774	AGATACTTATTTGTA[-/TTTAG]TTTAGTCATCTTTCA	81929
rs759294145	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12969556	AGCTGGGCGTGGTGG[C/T]GCGTGCCTGTAATCC	81929
rs759322061	snp	C/T	2.23167e-05	0.00334034	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985270	ACAAGCTAACTGGAG[C/T]AACTTTGCTGTTTTG	81929
rs759418325	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12962632	ACCACCACACCTGGC[-/T]TTTTTTTTTTTTTAG	81929
rs759418660	snp	G/T	2.14516e-05	0.00327496	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948106	CCTCTTCGGAGGCGC[G/T]GGCCCGACGGAAACC	81929
rs759491753	snp	A/G	1.75191e-05	0.0029596	missense, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948216	TGGCAACCTGCTCCA[A/G]CGATCAGAGCGTTAA	81929
rs759497448	in-del	-/TT			intron-variant	SEH1L	GRCh38.p7	18:12964634	ATTTACTCCCGTCTC[-/TT]TTTTTTTTTTTTTTT	81929
rs759632780	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12978054	GCTGGTCTTGAACTA[C/T]TGGGTTCAAGCAATT	81929
rs759688349	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976842	TTGGCCGGGCGTGGT[A/G]GCAGGCCCCTGTAGT	81929
rs759706897	snp	A/G	0.00011536	0.00759387	intron-variant	SEH1L	GRCh38.p7	18:12971145	ATGTTCTTTCTCCCC[A/G]TTTCTAGCTCTCGTG	81929
rs759723982	snp	A/C			intron-variant, synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12964439	TTATCATTAAAGAAT[A/C]TCCAAACTGATAGAA	81929
rs759794734	snp	C/G			intron-variant, stop-gained, nc-transcript-variant	SEH1L	GRCh38.p7	18:12964478	TAGAGCACATTTATA[C/G]AACTTCCACATCCCA	81929
rs759798128	in-del	-/GCCGCCGCC	7.61238e-05	0.00616896	cds-indel, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948077	CGCGCCGCCGCCGCT[-/GCCGCCGCC]ACTGTCCTCTTCGGA	81929
rs759823719	in-del	-/AAG			intron-variant	SEH1L	GRCh38.p7	18:12978676	GAGCAGTGTGAAAAA[-/AAG]GTGAGATGCAGTGAT	81929
rs759827567	snp	A/G	1.64792e-05	0.00287042	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955550	TTTGACCGAACAGCT[A/G]CTGTATGGGAAGAAA	81929
rs759945288	snp	C/T			downstream-variant-500B	SEH1L	GRCh38.p7	18:12987668	ATATATTTAAAAATA[C/T]ACGAATCTCTTGCCT	81929
rs760020112	snp	C/T	0.00272851	0.0368349	intron-variant	SEH1L	GRCh38.p7	18:12955442	TATCTGTTCTTTTCT[C/T]TTTTTTTTTTGATTC	81929
rs760046468	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12951389	CTTGACACATTCAAG[A/G]TTCTCAATGTAAATT	81929
rs760062235	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12972674	TCTTACACCTTCTAC[C/G]TTCCTAGATTGTTGG	81929
rs760074499	in-del	-/TTAT			intron-variant	SEH1L	GRCh38.p7	18:12955037	CAAATAAATCTAATG[-/TTAT]TTATTTTATTAGGTG	81929
rs760079312	snp	A/G/T	3.32847e-05	0.00407939	intron-variant	SEH1L	GRCh38.p7	18:12984024	ATGTTAATGTATTTG[A/G/T]TTATTTTCCTTTCAG	81929
rs760144336	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959158	TGTCTTCCTGGGGAA[A/G]ATACTATTCATATCC	81929
rs760185949	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971163	TCTAGCTCTCGTGCT[C/T]ATTCCCCCATGATCG	81929
rs760235253	snp	C/T	3.33578e-05	0.00408384	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987038	CTCTTAATCCCTTAC[C/T]TGAGAATGAAGGGAT	81929
rs760398202	snp	C/G	2.31254e-05	0.00340032	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948098	GCCACTGTCCTCTTC[C/G]GAGGCGCGGGCCCGA	81929
rs760573309	snp	G/T	1.64787e-05	0.00287038	stop-gained, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971232	AAGGTTCAGATTTTT[G/T]AATATAATGAAAACA	81929
rs760650151	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12959639	GTAAATGATTTGCAA[A/C]TATTTTCTCCCGTTC	81929
rs760743430	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12950075	GTCTGGCTCTGTCAC[C/G]CAGGCTGGAGTGCAG	81929
rs760800943	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12976765	GTCAGAAGATCGAGA[C/T]CATCCTGGCTAACAT	81929
rs760850658	snp	A/G	3.4031e-05	0.00412484	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986901	CCCACGGGCTGGATC[A/G]AGATGGTCCAGTTAT	81929
rs760882341	in-del	-/GGAA	1.96415e-05	0.00313375	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948266	GGCGGGGCCGACCCC[-/GGAA]GGAAGGAAGGGGAGT	81929
rs760895225	snp	G/T	1.65293e-05	0.00287479	missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12951888	AGTGGTGATTGGCAT[G/T]GTACTGCTAGCTGGA	81929
rs760963231	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963293	AGGCACCAGATGTTA[C/T]GAATCTCAGCCAGTG	81929
rs760966657	snp	A/G	1.68513e-05	0.00290265	intron-variant	SEH1L	GRCh38.p7	18:12982724	ATATTTCTGCTCTGC[A/G]ATTTTTACTTAAAAT	81929
rs760969561	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12955871	TATTTGATTTTACCT[A/G]TTAGTATATTTTATG	81929
rs760998473	in-del	-/TT	0.000111294	0.00745885	intron-variant	SEH1L	GRCh38.p7	18:12963148	TTTAAATTGTTATTA[-/TT]TTTTTTTTAGGTTAA	81929
rs761021256	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12963145	TAATTTAAATTGTTA[C/T]TATTTTTTTTTTAGG	81929
rs761129810	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12972267	TGAACTGAGGAAGAA[C/G]GGGGAAGGTGTTAAG	81929
rs761172901	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12963110	GTCTTTTCCACTCTA[C/T]CATGCTTTCTTTTTG	81929
rs761264688	snp	A/G	1.65089e-05	0.00287301	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986963	TGGTAGAGCACTCTT[A/G]CGATGCTGACACTGC	81929
rs761373129	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12971010	AGTGTGGCCATGTCA[G/T]CTATGTGGCAGAGAC	81929
rs761514619	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12950197	CGCCACCACGCCTGG[C/G]CAATTAAAACATTTT	81929
rs761533294	in-del	-/AG			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949050	TTTTTTAGTAGAGAC[-/AG]AGTTTCACCATGTGG	81929
rs761546237	snp	G/T	8.25975e-05	0.00642588	missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12951874	GGGATAAAAGTGAAA[G/T]TGGTGATTGGCATTG	81929
rs761549536	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12984484	AGTGAGAGGAAGGTT[A/G]TCTGGTTTAATGGTG	81929
rs761555319	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12959135	CATGTGCTTATTGGT[C/G]AATTGTATGTCTTCC	81929
rs761565691	snp	A/T			missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982582	GTGGCTCAGTTCGAT[A/T]ATCATAATTCTCAGG	81929
rs761599729	snp	A/G	1.86981e-05	0.00305756	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948251	CGCGCGGCGCTTGCG[A/G]GCGGGGCCGACCCCG	81929
rs761771046	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12978107	TGCTGGGATTACAGG[A/T]GTGAGCCACTGTGGC	81929
rs761928842	snp	C/T	7.17129e-05	0.00598759	intron-variant	SEH1L	GRCh38.p7	18:12963140	GTATATAATTTAAAT[C/T]GTTATTATTTTTTTT	81929
rs761938482	snp	C/T	3.29853e-05	0.00406098	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955582	AGTAGGAGAATCAAA[C/T]GATAAACTGCGAGGA	81929
rs761957485	in-del	-/TT	1.65567e-05	0.00287716	intron-variant	SEH1L	GRCh38.p7	18:12971116	TGAAATGTGTATTTC[-/TT]TTGTTATCTAAAATG	81929
rs762036284	snp	G/T	8.29016e-05	0.00643769	intron-variant	SEH1L	GRCh38.p7	18:12978909	TGAGTTTTAGAAGCA[G/T]TTATGAATTTGAAAA	81929
rs762052534	in-del	-/ATAATC			intron-variant	SEH1L	GRCh38.p7	18:12957520	GGGCAAGAACATAAT[-/ATAATC]TGTGTGCTGTTGAAG	81929
rs762118979	snp	C/T	4.50582e-05	0.00474627	intron-variant, synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985246	CTTTAACAGAAAGCA[C/T]AGCTGAGTACAAGCT	81929
rs762130922	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12968047	TGTGTTTTCTCAAAT[A/G]TCAGTTCTTTTCGTG	81929
rs762174021	snp	C/T	1.6607e-05	0.00288153	intron-variant	SEH1L	GRCh38.p7	18:12984200	TGGCAGGTAGGCTGC[C/T]TCATGGGAAAACTGG	81929
rs762286943	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12962812	CTTGCAGCATGCTTT[A/G]TGTGACAAAACTTCT	81929
rs762323947	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12976044	CAGATGGATAGAATA[G/T]CTGAGATTAGTTGTC	81929
rs762416227	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12983021	TTTATCAAATAAATT[G/T]CTTTAGACAATCCAT	81929
rs762467307	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12985026	ACAATTTCAGGTTAC[C/T]GTGGAAGATACCAGA	81929
rs762511243	snp	A/C			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947491	CTCCGCGCGCCTCGC[A/C]TGTGTCTGGGGGGAA	81929
rs762680365	snp	A/G	0.000297629	0.0121953	intron-variant	SEH1L	GRCh38.p7	18:12978896	AAAGCCTGTGAGGTG[A/G]GTTTTAGAAGCATTT	81929
rs762680499	snp	C/G	1.93737e-05	0.00311231	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948115	AGGCGCGGGCCCGAC[C/G]GAAACCATGTTTGTG	81929
rs762699246	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12970669	GCCTCAAATGATCCT[C/T]TCTCCTGAGTCTCTC	81929
rs762701006	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12961149	GGCTGCGTGTGCAGT[G/T]TGTTTACTGGAGTTG	81929
rs762733325	snp	A/T	3.29538e-05	0.00405904	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978791	TATGACAGTCACTGA[A/T]CCTGTTCATGATATT	81929
rs762748807	snp	A/G/T	3.29458e-05	0.00405857	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963330	GCAGCATGAGATCTC[A/G/T]TGTAAGCTAAGCTGT	81929
rs762850117	snp	C/T	2.26981e-05	0.00336876	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985294	TGTTTTGCTGCTTGT[C/T]GCATGCACACAGGAA	81929
rs762875648	snp	C/T	1.65132e-05	0.00287339	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986945	CTCCTCCTCCTCCTC[C/T]TCTGGTAGAGCACTC	81929
rs762882876	snp	A/T	1.64762e-05	0.00287016	intron-variant	SEH1L	GRCh38.p7	18:12955448	TTCTTTTCTTTTTTT[A/T]TTTTGATTCCCCAGA	81929
rs762892629	in-del	-/CGT	1.6483e-05	0.00287076	intron-variant	SEH1L	GRCh38.p7	18:12971144	AATGTTCTTTCTCCC[-/CGT]TTCTAGCTCTCGTGC	81929
rs762895918	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12969810	GACAGGAGAATCACT[C/T]GAACCCAGGAGGTGG	81929
rs763015548	snp	A/T	1.64814e-05	0.00287061	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984141	AATCCTTCCCTAGGT[A/T]CAACTATTCCAAGTC	81929
rs763031454	snp	A/G	1.65364e-05	0.0028754	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984176	GAATTCATTAAATGG[A/G]TCTTCTGCTGGCAGG	81929
rs763053880	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12966429	TTATGTATTTGTTTT[C/T]GAGACACGTGTCACT	81929
rs763083382	snp	A/G	1.64874e-05	0.00287113	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984062	TATGGACAATTGGAA[A/G]TGTACTGGTATTTTG	81929
rs763099850	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12964554	GTTGGAGTTATACTG[A/G]TAATTATTATAATTT	81929
rs763131080	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12952544	CAAGTAGAAATTTTC[A/C]TACCTTAAAAGTCAT	81929
rs763329101	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12981666	ATTTAGGCTGAAACT[-/A]AACAATTCTCCAAAT	81929
rs763355665	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12953558	CCACAAAAATCATTG[C/G]ATTTTGATTTGTATT	81929
rs763355952	snp	A/G	2.83748e-05	0.00376651	intron-variant	SEH1L	GRCh38.p7	18:12963131	TTTCTTTTTGTATAT[A/G]ATTTAAATTGTTATT	81929
rs763426418	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12976642	TAGGAATTATTGGTT[A/T]ATAGGTACTGAAACC	81929
rs763436965	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12975967	TGAATGTGGTAAGCA[C/G]AATTTATTTCAGACA	81929
rs763471600	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12960174	TTTTTCTTTACATGA[C/T]GCTGAAGTTATCTTC	81929
rs763545616	snp	C/T	3.29658e-05	0.00405978	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955569	TATGGGAAGAAATAG[C/T]AGGAGAATCAAATGA	81929
rs763563600	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12954504	CAAGTTCTTGCTCTG[A/T]CACCCAGGCTGGAGT	81929
rs763582993	snp	A/T	6.86711e-05	0.00585925	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985298	TTGCTGCTTGTTGCA[A/T]GCACACAGGAATGGA	81929
rs763603007	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12968495	TTTTGACCAAATCAC[G/T]CCATGATTGTCCGTG	81929
rs763700533	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12981649	TTCTCTTAACTGTGC[C/T]TTATTTAGGCTGAAA	81929
rs763709828	snp	C/G	1.6516e-05	0.00287362	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948245	AAGGTGCGCGCGGCG[C/G]TTGCGGGCGGGGCCG	81929
rs763769387	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947068	GCTCCTCCACTTTCC[A/G]GTTTTGGCAGAATCC	81929
rs763797230	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12983106	AGTTAAGAGCCTTGG[A/G]GGCCCTGATTGTAAG	81929
rs763904580	snp	C/T	2.03101e-05	0.00318664	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948127	GACGGAAACCATGTT[C/T]GTGGCTCGCAGCATC	81929
rs763906548	snp	C/T	1.65542e-05	0.00287695	intron-variant	SEH1L	GRCh38.p7	18:12978900	CCTGTGAGGTGAGTT[C/T]TAGAAGCATTTATGA	81929
rs763942996	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12958176	GCATTCTCCGCCTCC[A/G]GGGTTCAAGCGATTT	81929
rs763954851	snp	C/G/T	3.30138e-05	0.00406276	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986956	CCTCCTCTGGTAGAG[C/G/T]ACTCTTGCGATGCTG	81929
rs764022655	snp	G/T	1.64893e-05	0.0028713	missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963167	TTTTTTAGGTTAAAA[G/T]GACAACTCTGGTGGA	81929
rs764058717	snp	A/G	3.29734e-05	0.00406025	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955576	AGAAATAGTAGGAGA[A/G]TCAAATGATAAACTG	81929
rs764076722	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12952557	TCATACCTTAAAAGT[C/T]ATCCATTTTAAATGT	81929
rs764256537	snp	A/T	1.64827e-05	0.00287073	intron-variant	SEH1L	GRCh38.p7	18:12955454	TCTTTTTTTTTTTTG[A/T]TTCCCCAGACACATA	81929
rs764316367	in-del	-/TGT			intron-variant	SEH1L	GRCh38.p7	18:12974079	AACGAGGGGAAGTGG[-/TGT]TGGGGAAAGAGTGTC	81929
rs764326798	in-del	-/CT			downstream-variant-500B, utr-variant-3-prime	SEH1L	GRCh38.p7	18:12987552	TGTGGACTTTTTGGT[-/CT]TTTTTTTTTTTTTTT	81929
rs764410193	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12968589	GATGGTGATACGGAC[-/T]CTTTTTTCCTTTGTA	81929
rs764424406	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12951436	TGCTTTGTCTCCCAG[A/G]CTGGAGTGCAGTGGC	81929
rs764452520	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12966540	AAGTAACTGGGACTA[C/T]AGGCATTCACCACCA	81929
rs764530135	snp	A/G	0.000148276	0.00860907	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978804	GATCCTGTTCATGAT[A/G]TTGCATTCGCTCCAA	81929
rs764552400	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12960232	AACAGTTTATCATTA[C/T]ATTGTGGCAACAAGG	81929
rs764630924	in-del	-/TTA			intron-variant	SEH1L	GRCh38.p7	18:12982044	TTTTATTTTGTATTT[-/TTA]GTAGGGATGGGGTTT	81929
rs764854258	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12956097	TCACCCAGGCTGGAG[A/T]GCAGTGGCACAATCT	81929
rs764867974	in-del	-/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949214	TGAGATTTAGGAACC[-/T]TCCCAGATGTGTTGC	81929
rs764914932	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12963146	AATTTAAATTGTTAT[C/T]ATTTTTTTTTTAGGT	81929
rs764920382	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12959293	ATGCTAGGATCCAGA[A/C]ATGTTTTGGATTTTG	81929
rs764937072	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12974341	CTAGAGTGCAGTGGC[A/G]CAACCTTGGCTCGCT	81929
rs764939552	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12954226	GTTATTTGTTATTAT[A/G]CAGTATTTTCCCTGA	81929
rs764976565	snp	C/T	2.23107e-05	0.00333989	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985273	AGCTAACTGGAGTAA[C/T]TTTGCTGTTTTGCTG	81929
rs765064959	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12969589	GCCACTTGGGAGGCC[A/G]AGGCACGAGAATCGC	81929
rs765107040	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12982888	AACAGAGCAGTTTTC[A/G]AAACTAAAGTAATTA	81929
rs765182168	in-del	-/GAG			intron-variant, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949790	GAATTCAGTGGCATA[-/GAG]GAGCACAGCATTCAC	81929
rs765231354	in-del	-/A	1.6631e-05	0.00288362	intron-variant	SEH1L	GRCh38.p7	18:12951916	GGAAGGTTAGTATTT[-/A]TTTTTACATTTATTA	81929
rs765337378	in-del	-/TTATC	1.65451e-05	0.00287615	intron-variant	SEH1L	GRCh38.p7	18:12971121	TGTGTATTTCTTTTG[-/TTATC]TAAAATGTTCTTTCT	81929
rs765392405	snp	A/G	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982629	GAATATAACAGGAAC[A/G]GTGCTAGCATCTTCA	81929
rs765533016	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12963471	TCAAAGGTGCTTCTT[C/T]TCAAGATATATAGAG	81929
rs765557572	snp	A/T			missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12951873	TGGGATAAAAGTGAA[A/T]GTGGTGATTGGCATT	81929
rs765601208	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12952319	CTCACTGCAACCTCC[A/G]CCTGTTGGGTTCAAG	81929
rs765618012	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986049	GCTTCCTTCAAATCA[A/G]AATTTGGACACACAC	81929
rs765687047	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12974482	ATGGGGTTTCACCAT[C/T]TTGGCCAGGATGGTC	81929
rs765688546	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12973122	CTGAGGTGGGATGAT[C/G]ACCTGAGCCTGGGAG	81929
rs765753458	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12952394	TGCACCACGATGCCC[A/G]GCTAATTTTTGTGTT	81929
rs765840726	snp	C/T	3.29489e-05	0.00405874	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971167	GCTCTCGTGCTCATT[C/T]CCCCATGATCGCCGT	81929
rs765887619	snp	A/G	3.34711e-05	0.00409078	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987042	TAATCCCTTACCTGA[A/G]AATGAAGGGATTTAA	81929
rs765895395	snp	A/G	1.64795e-05	0.00287045	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971236	TTCAGATTTTTGAAT[A/G]TAATGAAAACACCAG	81929
rs765898259	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12971340	TTACAGAATTATGTG[G/T]CATTCATCATATGTT	81929
rs765910089	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959271	GGTTGAGTATTCCTT[A/G]TCCATAATGCTAGGA	81929
rs765963470	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976888	GGCTGAGGCAGGAGA[A/G]TGGCATGAACCTGGG	81929
rs765997840	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12958529	ATGCCTCCCCCTTCC[G/T]CCTCCCTCTACCCCC	81929
rs766094718	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12972804	AAAACTATGAGCCCT[A/C]TTAATAGCACATTTT	81929
rs766112532	in-del	-/T	1.65529e-05	0.00287683	intron-variant	SEH1L	GRCh38.p7	18:12971267	TCAGTCCTGCTTTGG[-/T]TTTTAATAATTGTTC	81929
rs766262068	snp	C/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946727	AAGAGGTGGGGCCCA[C/T]CTCTTAAAGTAGCAA	81929
rs766262328	snp	C/T	1.67787e-05	0.00289639	intron-variant	SEH1L	GRCh38.p7	18:12984222	GAAAACTGGAAATCA[C/T]CTTTGTTTTAAATCA	81929
rs766272663	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12966614	GCCTTGTTGCCCAGA[A/G]TGGTGTTGAACTCCT	81929
rs766301628	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12978185	TAAATGTACATTATT[A/G]AAGGAGGAAACGTGG	81929
rs766441099	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12961405	AAGTTTAACAACTGC[C/G]TGATCATCACCTGAT	81929
rs766488737	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12950362	TTTATTCCAGAGTAC[-/T]TTTTTTTTTAAAGGA	81929
rs766569619	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12955978	GCTGAGATTATAGGC[A/G]TGAGCCACTGTGCCT	81929
rs766618034	snp	G/T	1.75059e-05	0.00295849	intron-variant	SEH1L	GRCh38.p7	18:12955438	TGAGTATCTGTTCTT[G/T]TCTTTTTTTTTTTTG	81929
rs766686217	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963303	TGTTATGAATCTCAG[C/T]CAGTGGTCTTTGCAG	81929
rs766734368	snp	A/T	5.9638e-05	0.00546035	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948269	GGGGCCGACCCCGGA[A/T]GGAAGGAAGGGGAGT	81929
rs766792403	snp	A/G	1.65323e-05	0.00287505	missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12951891	GGTGATTGGCATTGT[A/G]CTGCTAGCTGGAAGG	81929
rs766853254	snp	G/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985886	TACAGTTTGTAGCCA[G/T]GTTAAGCATTTGGTA	81929
rs766858932	snp	C/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948428	GGCCTCGCGGGCCGC[C/T]CTCCCGTGCGCCTGC	81929
rs766874892	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12972518	GCACTTGTCAGGTGA[G/T]CAGATGGGCTTCGCA	81929
rs766897487	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12950513	TTTCCTTTAACGTTT[C/T]AAGTTGTCATGGTAG	81929
rs766968508	snp	C/G/T	3.30171e-05	0.00406296	missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986964	GGTAGAGCACTCTTG[C/G/T]GATGCTGACACTGCC	81929
rs766988737	in-del	-/A			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947591	TTTCTTCATTTGCAC[-/A]GTATACCAATAAGCT	81929
rs767001820	snp	C/T	1.64768e-05	0.00287021	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963364	TGTATTTCTTGGAAC[C/T]CTTCAAGGTAAGTTT	81929
rs767019805	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12950237	GGCAGGGTCTTGCTG[C/T]GTTGCCCAGGCTAGT	81929
rs767039913	snp	C/T	6.6454e-05	0.0057639	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987032	CTCGGCCTCTTAATC[C/T]CTTACCTGAGAATGA	81929
rs767376115	snp	A/G	4.94262e-05	0.00497098	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971158	CCGTTTCTAGCTCTC[A/G]TGCTCATTCCCCCAT	81929
rs767393118	in-del	-/TGTGATTA			intron-variant	SEH1L	GRCh38.p7	18:12957975	GGCCTCCCAAAGTGC[-/TGTGATTA]TGTGATTATAGGCGT	81929
rs767425397	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12978115	TTACAGGTGTGAGCC[A/C]CTGTGGCCAGCCAAG	81929
rs767730077	snp	A/T	4.62011e-05	0.00480608	intron-variant	SEH1L	GRCh38.p7	18:12963143	TATAATTTAAATTGT[A/T]ATTATTTTTTTTTTA	81929
rs767777413	snp	A/C			missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984115	ATGGGAGTTCTCAGC[A/C]GGGAACCTCAAATCC	81929
rs767778886	snp	A/G	2.23761e-05	0.00334478	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985253	AGAAAGCACAGCTGA[A/G]TACAAGCTAACTGGA	81929
rs767837357	in-del	-/GCC			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948076	CGCGCCGCCGCCGCT[-/GCC]GCCGCCGCCACTGTC	81929
rs767854326	snp	A/G	1.6476e-05	0.00287014	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978813	CATGATATTGCATTC[A/G]CTCCAAATTTGGGAA	81929
rs767875721	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12953702	TAAAATTAATAATTT[C/G]AGAGTAAACAATTAA	81929
rs767902585	snp	A/G	1.88585e-05	0.00307065	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948254	GCGGCGCTTGCGGGC[A/G]GGGCCGACCCCGGAA	81929
rs767957856	snp	A/T	1.65864e-05	0.00287974	intron-variant	SEH1L	GRCh38.p7	18:12978911	AGTTTTAGAAGCATT[A/T]ATGAATTTGAAAATA	81929
rs767964977	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976053	AGAATAGCTGAGATT[A/G]GTTGTCTATTGCTGC	81929
rs768019548	snp	A/G	1.66618e-05	0.00288628	intron-variant	SEH1L	GRCh38.p7	18:12982701	AGTGAAGGGGTAATT[A/G]TTGGTTTATATTTCT	81929
rs768057778	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12983089	CTCTGCAGCTCCCAT[-/A]AAGTTAAGAGCCTTG	81929
rs768234076	snp	A/C	1.64751e-05	0.00287007	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982574	TCCATATAGTGGCTC[A/C]GTTCGATAATCATAA	81929
rs768249709	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12949975	ATAAATAGAATCATA[A/G]AATATTCGCCCTTTT	81929
rs768251830	snp	A/G	1.65201e-05	0.00287398	missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12951855	TTTATTTTCTTATAG[A/G]TCTGGGATAAAAGTG	81929
rs768265097	in-del	-/TTC			intron-variant	SEH1L	GRCh38.p7	18:12970416	CTGTCCATCTGTTTT[-/TTC]TTCTTCTTTTCTTTT	81929
rs768316859	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12963892	TAATTTTTGCATTTT[C/T]AGTAGACATGGGGTT	81929
rs768387265	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12962765	GGTGTAAGCCATCAC[A/G]CCCAACTCATTTACA	81929
rs768462017	snp	C/T	1.65457e-05	0.00287621	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987013	CCTCGCAGACGATAT[C/T]TCTCTCGGCCTCTTA	81929
rs768466666	snp	A/T	1.64776e-05	0.00287028	intron-variant	SEH1L	GRCh38.p7	18:12971150	CTTTCTCCCCGTTTC[A/T]AGCTCTCGTGCTCAT	81929
rs768485375	in-del	-/CTG	9.9249e-05	0.00704377	cds-indel, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984181	CATTAAATGGATCTT[-/CTG]CTGGCAGGTAGGCTG	81929
rs768623777	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12970764	TAAGATCTTTTTGTC[A/G]TGAAGTTAGTCACAG	81929
rs768675788	in-del	-/TTT			downstream-variant-500B, cds-indel	SEH1L	GRCh38.p7	18:12987553	GTGGACTTTTTGGTC[-/TTT]TTTTTTTTTTTTTTT	81929
rs768679522	snp	A/G			missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987008	CTCACCCTCGCAGAC[A/G]ATATCTCTCTCGGCC	81929
rs768841794	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12983813	GATGGGTGGTGAAAG[C/G]TTTATATTTTTAAAA	81929
rs768844107	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12967900	GCCTGGGCAACAGAG[C/T]GAGACTGTCTCAAAA	81929
rs768871228	snp	C/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947328	CTACTACTTCTGATC[C/G]TTTCCTCCCCGTCCA	81929
rs768917134	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963242	TGGGTCTTATGTTAG[C/T]AACCTGTTCCGCAGA	81929
rs768928236	snp	C/G	2.46612e-05	0.00351141	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948085	CGCCGCTGCCGCCGC[C/G]ACTGTCCTCTTCGGA	81929
rs768956545	in-del	-/TTT	7.14822e-05	0.00597796	intron-variant	SEH1L	GRCh38.p7	18:12963148	TTTAAATTGTTATTA[-/TTT]TTTTTTTAGGTTAAA	81929
rs769046151	in-del	-/TCC	0.0389757	0.134048	cds-indel, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986928	TTATGCCCAGCTCCT[-/TCC]TCCTCCTCCTCCTCC	81929
rs769149368	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12953604	GTTGATTATTTTTTC[A/T]TATGCTTATTTACCA	81929
rs769218084	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12968877	TACAATTGAGGTAAT[C/T]CTCAATTCAGGTTGC	81929
rs769274336	snp	G/T	2.70018e-05	0.00367426	intron-variant	SEH1L	GRCh38.p7	18:12963134	CTTTTTGTATATAAT[G/T]TAAATTGTTATTATT	81929
rs769395799	snp	C/T	1.65083e-05	0.00287296	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978886	TTTTTACATTAAAGC[C/T]TGTGAGGTGAGTTTT	81929
rs769418474	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12961144	GGAGGGGCTGCGTGT[A/G]CAGTGTGTTTACTGG	81929
rs769418571	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976538	AAACACGTTCTGGCT[A/G]CAGCATGTGTGCTCT	81929
rs769452441	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12950959	CTTGAGTAGCTGGGA[C/G]TACAGGTGTGCACCA	81929
rs769613021	snp	C/G			intron-variant, nc-transcript-variant	SEH1L	GRCh38.p7	18:12975791	GGGATGAATGCAGTA[C/G]CCCACTATGATGTGG	81929
rs769640302	snp	C/T	0.000148276	0.00860907	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982628	GGAATATAACAGGAA[C/T]GGTGCTAGCATCTTC	81929
rs769677753	snp	A/C	3.58809e-05	0.00423546	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948236	CAGAGCGTTAAGGTG[A/C]GCGCGGCGCTTGCGG	81929
rs769780772	in-del	-/C	1.65113e-05	0.00287322	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986977	GCGATGCTGACACTG[-/C]CCAACCTCCAGTATC	81929
rs769798536	snp	C/T			intron-variant, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949787	TGTAGAATTCAGTGG[C/T]ATAGAGCACAGCATT	81929
rs769877776	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12971055	AGTGTGACAGGCTAA[C/G]TGTAAGCTGGTTGTC	81929
rs769880138	snp	C/T	7.59004e-05	0.0061599	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948079	CGCCGCCGCCGCTGC[C/T]GCCGCCACTGTCCTC	81929
rs769908639	snp	C/T	1.64808e-05	0.00287057	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982560	AACAAAGTTTGAAAT[C/T]CATATAGTGGCTCAG	81929
rs769917144	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12978607	CAGGACTTGGACATA[C/T]TCTTTTGGGGGCTGC	81929
rs769931503	snp	A/T	0.00015488	0.00879864	intron-variant	SEH1L	GRCh38.p7	18:12978705	TGATGTGTGGATTTT[A/T]GCACATTTTATTTCT	81929
rs769937844	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12974030	TAGCTGCAAGAGAGT[A/G]AGACAGCAAGTGTCT	81929
rs770069655	snp	A/C	3.51784e-05	0.0041938	intron-variant	SEH1L	GRCh38.p7	18:12984279	TATTTCATGGATTAT[A/C]AGATGGAGTGGAAAT	81929
rs770141685	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12982195	TAAATTAATTATTGT[C/T]ATCTATTTTATTCTT	81929
rs770155230	snp	C/T	0.000115351	0.00759355	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955554	ACCGAACAGCTGCTG[C/T]ATGGGAAGAAATAGT	81929
rs770235667	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12967621	TGCCGATGAATGACC[A/G]TGAAAGCCTGGGCCG	81929
rs770250498	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12954557	CTGCAGCCTCAACCT[G/T]CCAGGCTGAAGTGAT	81929
rs770547419	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12974222	TTATTTAGATTGAAC[A/G]TGGAGGAGATGTGAT	81929
rs770598627	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12953416	TAGCTTTCTAAGAAA[C/T]TGCGAAACTCTTCCA	81929
rs770686951	snp	C/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949701	CTCGTGATCCGCCCA[C/G]CTCGGCCTCCCAAAG	81929
rs770719649	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12959649	TGCAAATATTTTCTC[C/G]CGTTCTGTGGGTTGC	81929
rs770729524	snp	A/G	2.24732e-05	0.00335203	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948101	ACTGTCCTCTTCGGA[A/G]GCGCGGGCCCGACGG	81929
rs770769506	snp	G/T	1.64806e-05	0.00287054	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978864	ATAGCGACCAAAGAT[G/T]TGAGAATTTTTACAT	81929
rs770844641	snp	A/G	1.64947e-05	0.00287177	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978759	TCCATTAGGAAATAT[A/G]CAAAAGCTGAAACTC	81929
rs770926470	snp	C/T	1.64833e-05	0.00287078	intron-variant	SEH1L	GRCh38.p7	18:12971142	AAAATGTTCTTTCTC[C/T]CCGTTTCTAGCTCTC	81929
rs771000556	snp	C/T	3.29468e-05	0.00405861	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971201	AAGTGATGACAGTAG[C/T]CCCAACGCAATGGCC	81929
rs771004200	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12970543	CTCCTGCCTCAGCTC[C/T]TGAGTAGCTGAGACA	81929
rs771008612	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12959023	TTGTTGTGGTGCTAT[G/T]TATTGTAGCCATCCT	81929
rs771128663	snp	A/G	0.000115633	0.00760283	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987002	AGTATCCTCACCCTC[A/G]CAGACGATATCTCTC	81929
rs771312010	snp	C/T	3.35284e-05	0.00409427	intron-variant	SEH1L	GRCh38.p7	18:12984010	CATTGGTATTAATCA[C/T]GTTAATGTATTTGAT	81929
rs771346876	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12952060	TAAAGTAACAACTGT[A/G]TTTCTCAGAATTTGA	81929
rs771447423	snp	C/T	1.64738e-05	0.00286995	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955518	CTGAATTTGGGCAGG[C/T]TTTGGCTTCCTGTTC	81929
rs771476203	snp	A/G			utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987223	TAAATCTGTTTGTGC[A/G]TCTGCATCAAAGGAA	81929
rs771477580	in-del	-/TGGTTACGCTAAACTCTGAAGCAACTCTCCAACTATCAGCACT	1.67388e-05	0.00289294	intron-variant	SEH1L	GRCh38.p7	18:12955650	ACCGGGAAGACATGA[lengthTooLong]GCAGCCAAGGAGCAT	81929
rs771687004	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12964265	GTAAAGTTCCTTTAC[C/T]CCCTAAAAACAAATG	81929
rs771789390	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12951144	GGAGTGGTGAAAAAG[G/T]TTGAGTCTCAGGACA	81929
rs771820310	snp	C/T	1.67214e-05	0.00289144	intron-variant	SEH1L	GRCh38.p7	18:12982707	GGGGTAATTGTTGGT[C/T]TATATTTCTGCTCTG	81929
rs771825366	snp	A/C	1.69324e-05	0.00290962	intron-variant	SEH1L	GRCh38.p7	18:12978724	CATTTTATTTCTAAA[A/C]TGTTAATGTCAATTG	81929
rs771846054	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12972613	ACTAGTGTTACTCCC[A/G]TGGGCTCTGCAATTC	81929
rs771851777	in-del	-/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986040	CATGGCTTAGCTTCC[-/T]TCAAATCAAAATTTG	81929
rs771878349	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971220	AACGCAATGGCCAAG[A/G]TTCAGATTTTTGAAT	81929
rs771912994	snp	C/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946554	CAACCAATGATCTGT[C/T]TACTGTCTGTATTTA	81929
rs771919182	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12960705	TGTCAGTTCAGTATA[C/T]TATAGATTGGATTTG	81929
rs772251875	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963253	TTAGCAACCTGTTCC[A/G]CAGATGGTATAGTAA	81929
rs772296944	snp	C/T	1.74148e-05	0.00295078	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986895	GGATTCCCCACGGGC[C/T]GGATCGAGATGGTCC	81929
rs772299912	snp	A/G	4.94246e-05	0.0049709	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982586	CTCAGTTCGATAATC[A/G]TAATTCTCAGGTCTG	81929
rs772497914	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12974751	ACCGGGCATTTTTAT[A/G]TGTGTTATGAAGTTT	81929
rs772579987	in-del	-/T	2.40486e-05	0.00346752	intron-variant	SEH1L	GRCh38.p7	18:12985211	GTGATGCATTTTCCC[-/T]TTTCCATTTGTATTA	81929
rs772605180	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976688	ATGCATATTCTGGCC[A/G]GGCGCAGTGGCTCAC	81929
rs772607802	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12957342	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG	81929
rs772613795	in-del	-/TT			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948839	TTCCGACAAGCAGAA[-/TT]TTTCTTTTCTTTTTT	81929
rs772693574	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12951194	AAACCAGGCGATACT[C/G]TATTTTGGCTCATAC	81929
rs772728252	snp	C/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985792	GTACAACTCTGTCAT[C/T]TCTTTGTAATATTTA	81929
rs772759424	snp	A/G	1.65135e-05	0.00287341	intron-variant	SEH1L	GRCh38.p7	18:12971127	TTTCTTTTGTTATCT[A/G]AAATGTTCTTTCTCC	81929
rs772800744	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12972664	ACCAAGGGGATCTTA[C/T]ACCTTCTACCTTCCT	81929
rs772832528	snp	A/C/G	3.33501e-05	0.0040834	intron-variant	SEH1L	GRCh38.p7	18:12982704	GAAGGGGTAATTGTT[A/C/G]GTTTATATTTCTGCT	81929
rs772992074	snp	A/C	4.68735e-05	0.00484093	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948097	CGCCACTGTCCTCTT[A/C]GGAGGCGCGGGCCCG	81929
rs773004722	snp	C/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946671	TTTGGAAATGAGTGT[C/T]TTTGACCTTCAAAAA	81929
rs773091267	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12964142	GCATAGAGCATGACT[A/G]TATGAATATTACCAT	81929
rs773091561	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959610	CAGATTTTTGGATTT[A/G]ATATGCACAACCTGT	81929
rs773112779	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12959151	AATTGTATGTCTTCC[C/T]GGGGAAAATACTATT	81929
rs773301081	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12972140	GACAGTCCAGGTGGG[A/G]GAGTACGTGGCTTTG	81929
rs773316659	snp	A/C	2.23631e-05	0.00334381	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985258	GCACAGCTGAGTACA[A/C]GCTAACTGGAGTAAC	81929
rs773359900	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12970517	CCTCCAACTCCTGGG[C/T]GCAAGTGATCCTCCT	81929
rs773439892	snp	C/T	1.7119e-05	0.00292562	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986900	CCCCACGGGCTGGAT[C/T]GAGATGGTCCAGTTA	81929
rs773477986	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963264	TTCCGCAGATGGTAT[A/G]GTAAGAATCTATGAG	81929
rs773483250	snp	C/T			intron-variant, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949891	AAGAGCACCCTGTTC[C/T]GCCACCCCATCCTCT	81929
rs773532745	snp	A/G	4.57362e-05	0.00478184	intron-variant	SEH1L	GRCh38.p7	18:12963144	ATAATTTAAATTGTT[A/G]TTATTTTTTTTTTAG	81929
rs773681200	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982604	ATTCTCAGGTCTGGC[A/G]AGTGAGTTGGAATAT	81929
rs773773623	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12963034	GTGGCCCAGAGATGT[A/G]TCCAAGCTTATATAC	81929
rs773773844	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12977887	AGGCTGGAGTGCAGT[G/T]GCGTAATCTCAGCTC	81929
rs773810241	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12963900	GCATTTTTAGTAGAC[A/G]TGGGGTTTTACCATG	81929
rs773834028	snp	G/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982575	CCATATAGTGGCTCA[G/T]TTCGATAATCATAAT	81929
rs773844299	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12962787	TCATTTACAGTTAAA[A/G]GGTCTAATGCTTGCA	81929
rs773944563	snp	C/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985628	TTCATTTGGAAAATA[C/T]AGACATATTTCTTTT	81929
rs774053676	snp	A/C	3.30382e-05	0.00406423	missense, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12951862	TCTTATAGGTCTGGG[A/C]TAAAAGTGAAAGTGG	81929
rs774066539	snp	A/G	3.31087e-05	0.00406857	intron-variant	SEH1L	GRCh38.p7	18:12978902	TGTGAGGTGAGTTTT[A/G]GAAGCATTTATGAAT	81929
rs774134493	snp	A/C			utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987089	TGAAAGGCCTTATTC[A/C]AGTGCTTGTAAATGC	81929
rs774135084	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12959128	TTATTTTCATGTGCT[A/T]ATTGGTCAATTGTAT	81929
rs774180018	snp	G/T	1.64768e-05	0.00287021	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971154	CTCCCCGTTTCTAGC[G/T]CTCGTGCTCATTCCC	81929
rs774213071	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12950033	TTTTTTTTTTCTTTT[C/T]TCTTTTTCCTTTTTT	81929
rs774233064	snp	C/T	1.65455e-05	0.00287619	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987015	TCGCAGACGATATCT[C/T]TCTCGGCCTCTTAAT	81929
rs774251412	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12970810	TTTCATAGTTAATGA[C/T]CAAAAATTTCAGGAG	81929
rs774328926	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12958186	CCTCCGGGGTTCAAG[C/T]GATTTTCCTGCCTCA	81929
rs774603314	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976677	GTGTAGAAACCATGC[A/G]TATTCTGGCCGGGCG	81929
rs774628625	snp	C/T	2.30062e-05	0.00339155	intron-variant	SEH1L	GRCh38.p7	18:12985234	TTGTATTATGTCCTT[C/T]AACAGAAAGCACAGC	81929
rs774683633	snp	C/T	3.31791e-05	0.00407289	intron-variant	SEH1L	GRCh38.p7	18:12984196	CTGCTGGCAGGTAGG[C/T]TGCTTCATGGGAAAA	81929
rs774691653	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12982459	TATATATGTGTGTGT[A/G]TATATATATGTTTTA	81929
rs774788193	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12981985	ATGCCTCAGCCTCCT[A/G]AGTAGCTGGGACTAC	81929
rs774819709	in-del	-/GCT			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948073	CCACGCGCCGCCGCC[-/GCT]GCTGCCGCCGCCACT	81929
rs774876682	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963244	GGTCTTATGTTAGCA[A/G]CCTGTTCCGCAGATG	81929
rs774987725	snp	C/T			intron-variant, nc-transcript-variant	SEH1L	GRCh38.p7	18:12975822	AATGAGGACATGCAC[C/T]GTGGCGTGGGATGAA	81929
rs775059202	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12960082	TTTGGTCTCAGGTAA[C/T]GCCTTGAGCAACCAG	81929
rs775060873	snp	C/T	1.80406e-05	0.00300333	intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12948238	GAGCGTTAAGGTGCG[C/T]GCGGCGCTTGCGGGC	81929
rs775175073	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12963490	AGATATATAGAGTAT[A/G]TGTTCTCCATTTTTC	81929
rs775201532	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985521	CCAAAACAATTTTTT[A/G]AAATGTTCCTGAAAC	81929
rs775210345	snp	C/T	1.78274e-05	0.00298553	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986929	TATGCCCAGCTCCTT[C/T]CTCCTCCTCCTCCTC	81929
rs775241546	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978788	TCTTATGACAGTCAC[C/T]GATCCTGTTCATGAT	81929
rs775274339	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12970402	TTTCCACTTTTCCCC[-/T]GTCCATCTGTTTTTT	81929
rs775352541	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12961148	GGGCTGCGTGTGCAG[C/T]GTGTTTACTGGAGTT	81929
rs775509752	snp	C/T	1.65888e-05	0.00287996	intron-variant	SEH1L	GRCh38.p7	18:12951849	CTGCCTTTTATTTTC[C/T]TATAGGTCTGGGATA	81929
rs775518137	snp	C/G			intron-variant, utr-variant-5-prime	SEH1L	GRCh38.p7	18:12949848	TCTCCAGAACCTTTT[C/G]ATCATCCTAAACTGA	81929
rs775570572	in-del	-/TG	2.44927e-05	0.00349939	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948088	CGCTGCCGCCGCCAC[-/TG]TCCTCTTCGGAGGCG	81929
rs775694610	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971210	CAGTAGCCCCAACGC[A/G]ATGGCCAAGGTTCAG	81929
rs775790312	in-del	-/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946596	AACAATTTTTAAACT[-/G]TTTTGATATTTTTAT	81929
rs775811852	snp	A/G	1.64822e-05	0.00287068	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955567	TGTATGGGAAGAAAT[A/G]GTAGGAGAATCAAAT	81929
rs775828298	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12954473	ACTTTTGAAGCAAAT[A/G]ATTTTTTTTTGGAGA	81929
rs775829011	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12968514	TGATTGTCCGTGACT[C/T]ATTTATATTCTTTGC	81929
rs775864624	in-del	-/T	0.132653	0.220748	intron-variant	SEH1L	GRCh38.p7	18:12963147	TTTAAATTGTTATTA[-/T]TTTTTTTTTTAGGTT	81929
rs775867104	snp	A/G	3.30126e-05	0.00406266	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984153	GGTTCAACTATTCCA[A/G]GTCTTCAGAATTCAT	81929
rs775956810	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12974438	GCACCCGCCACCATG[C/G]CCAGCTAACTTTTGT	81929
rs775973024	snp	A/G	2.95068e-05	0.0038409	intron-variant	SEH1L	GRCh38.p7	18:12963127	ATGCTTTCTTTTTGT[A/G]TATAATTTAAATTGT	81929
rs776016117	snp	A/G	1.76393e-05	0.00296974	intron-variant	SEH1L	GRCh38.p7	18:12984281	TTTCATGGATTATAA[A/G]ATGGAGTGGAAATGT	81929
rs776120003	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12952320	TCACTGCAACCTCCG[C/G]CTGTTGGGTTCAAGT	81929
rs776166381	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12964635	TTTACTCCCGTCTCT[-/T]TTTTTTTTTTTTTTT	81929
rs776212363	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12959651	CAAATATTTTCTCCC[A/G]TTCTGTGGGTTGCCT	81929
rs776291342	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12975492	CAGCTGATGATGTTT[C/G]AGCATGAATCTTGAA	81929
rs776327419	snp	A/C	1.7393e-05	0.00294893	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948194	TTCGACTTCCACGGG[A/C]GGCGGATGGCAACCT	81929
rs776379920	snp	A/C	3.29832e-05	0.00406085	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978878	TGTGAGAATTTTTAC[A/C]TTAAAGCCTGTGAGG	81929
rs776477612	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947438	GTCCCGACGGAGCGC[A/G]GCTCCTGACCAAACC	81929
rs776491899	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12974247	TGTGATAGTGGACTA[C/T]GTAGTATCGTTATTA	81929
rs776580049	snp	C/G	2.18005e-05	0.00330148	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948105	TCCTCTTCGGAGGCG[C/G]GGGCCCGACGGAAAC	81929
rs776584350	snp	A/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946788	GGTCATTGCGCCACT[A/T]CTCTTTGCAGGTTTC	81929
rs776593881	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12978035	GTCTTGCTGTGTTGC[A/G]CAGGCTGGTCTTGAA	81929
rs776631192	snp	A/C	1.64808e-05	0.00287057	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978777	AAAGCTGAAACTCTT[A/C]TGACAGTCACTGATC	81929
rs776720532	snp	A/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963322	TGGTCTTTGCAGCAT[A/G]AGATCTCATGTAAGC	81929
rs776771917	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12968368	CACGATGAACCATTG[G/T]GGCGCAGTTCCTTCC	81929
rs776782017	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12959035	TATTTATTGTAGCCA[C/T]CCTAGTGACTGTGTT	81929
rs776822220	in-del	-/AAAG			intron-variant	SEH1L	GRCh38.p7	18:12978675	TGAGCAGTGTGAAAA[-/AAAG]GTGAGATGCAGTGAT	81929
rs776862905	snp	C/T	4.94491e-05	0.00497213	intron-variant	SEH1L	GRCh38.p7	18:12971144	AATGTTCTTTCTCCC[C/T]GTTTCTAGCTCTCGT	81929
rs776887211	in-del	-/ACATATTAAACCTCTGATA	1.64879e-05	0.00287118	intron-variant	SEH1L	GRCh38.p7	18:12963379	CTTCAAGGTAAGTTT[-/ACATATTAAACCTCTGATA]ACATATTAAACCTCT	81929
rs776918239	snp	C/T	0.000132199	0.00812907	stop-gained, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987007	CCTCACCCTCGCAGA[C/T]GATATCTCTCTCGGC	81929
rs776975228	in-del	-/TCC/TCCTCC	0.0391591	0.134357	cds-indel, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986927	TTATGCCCAGCTCCT[-/TCC/TCCTCC]TCCTCCTCCTCCTCC	81929
rs776978394	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12976435	CAGGAGGTGCGGGTC[A/G]TGGGGGCACTTAGAA	81929
rs776980370	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12952372	CAAGTAGCTGGGACT[A/G]TAGGCGTGCACCACG	81929
rs777086688	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12964385	TATCTTTTTTTTAAA[A/C]ATTTTTATTCTGCTA	81929
rs777104900	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12950458	TGAAAAAATTATAGA[C/T]TTATTGCTAATGTGT	81929
rs777109525	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12967839	GAATCGCTTGAACTT[C/G]GGAGATGAAGGTTGC	81929
rs777129983	snp	C/T	1.66779e-05	0.00288768	intron-variant	SEH1L	GRCh38.p7	18:12955637	TTAGTATTCTGGGGA[C/T]CGGGAAGACATGAGC	81929
rs777269939	in-del	-/A	1.68012e-05	0.00289833	intron-variant	SEH1L	GRCh38.p7	18:12984005	TTAGGCATTGGTATT[-/A]ATCATGTTAATGTAT	81929
rs777362135	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12981994	CCTCCTGAGTAGCTG[G/T]GACTACAGGCGCCCG	81929
rs777362226	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12965710	GTTTTAGGATTTTGC[C/G]TTATTATTCTGAGCT	81929
rs777379692	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955522	ATTTGGGCAGGTTTT[A/G]GCTTCCTGTTCTTTT	81929
rs777430821	snp	G/T			intron-variant	SEH1L	GRCh38.p7	18:12976426	CGGGACCACCAGGAG[G/T]TGCGGGTCATGGGGG	81929
rs777447750	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12967202	AATACAGGGTTTCCA[C/G]AAGTCTCTCACTACA	81929
rs777624374	snp	C/T	1.64792e-05	0.00287042	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978856	TTCTAGCAATAGCGA[C/T]CAAAGATGTGAGAAT	81929
rs777695284	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12956323	CTGGGATTACAGGCG[C/T]GAGCCACCACGCCTG	81929
rs777769068	snp	C/T	6.60622e-05	0.00574689	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986998	CTCCAGTATCCTCAC[C/T]CTCGCAGACGATATC	81929
rs777824193	snp	G/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985275	CTAACTGGAGTAACT[G/T]TGCTGTTTTGCTGCT	81929
rs777907389	snp	A/G	6.98129e-05	0.00590776	utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987093	AGGCCTTATTCAAGT[A/G]CTTGTAAATGCTTTC	81929
rs777925948	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12972002	TAAGAAGTAATGTCC[A/G]TTGTTTCAGTTTTAT	81929
rs777936793	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12978019	TTTTTGTAAAGATGG[A/G]GTCTTGCTGTGTTGC	81929
rs777955827	in-del	-/TCTC			frameshift-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12987012	CCCTCGCAGACGATA[-/TCTC]TCTCGGCCTCTTAAT	81929
rs778025117	snp	C/T			intron-variant, nc-transcript-variant	SEH1L	GRCh38.p7	18:12975882	ACCAGCTGTAGGTCA[C/T]GTGAGTCTTGGTTTC	81929
rs778112188	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986277	AAGAAGAATAACAGT[A/G]GGGCACAGTCATTCT	81929
rs778160613	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12962552	TGCTCACTGTACCTT[C/T]TGCCCCACTGGCTCA	81929
rs778279224	snp	A/G	3.29582e-05	0.00405931	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12984102	GGGAGCCCAGTCAAT[A/G]GGAGTTCTCAGCAGG	81929
rs778312637	snp	G/T	1.67052e-05	0.00289004	intron-variant	SEH1L	GRCh38.p7	18:12971280	TGGTTTTAATAATTG[G/T]TCAGAATTGCATTTA	81929
rs778371919	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12958962	CATTTTACATTCCTA[C/T]CAGCAATGCTCAAGG	81929
rs778469978	in-del	-/CTCA			intron-variant	SEH1L	GRCh38.p7	18:12974309	TCTTTGAGATGGAGT[-/CTCA]CTCTGTTTCCAGGCT	81929
rs778596225	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12977729	TCAAAAAAACCTCAA[C/T]TCCTGTTACCAGCTT	81929
rs778858196	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12966891	AGATTTAGTACTCCA[A/T]CTCCCAGATCTCCAC	81929
rs778887175	snp	A/G	1.65312e-05	0.00287495	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955601	AAACTGCGAGGACAG[A/G]GCCACTGGGTGAGAC	81929
rs778923576	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12951369	CCTTGGTGCTTGGCC[C/T]AGTGCTTGACACATT	81929
rs778940102	snp	C/G	1.64735e-05	0.00286993	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12955514	CATCCTGAATTTGGG[C/G]AGGTTTTGGCTTCCT	81929
rs778941220	snp	C/G	1.65968e-05	0.00288065	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982525	ATTAACAGGAAAGAA[C/G]TGACTTCCTCTGGTG	81929
rs778956584	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12951648	CGTTTGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT	81929
rs778992154	snp	A/C	1.65329e-05	0.0028751	intron-variant	SEH1L	GRCh38.p7	18:12951805	TTATAGTTTTTGTAT[A/C]AATTTGTAGGAATTT	81929
rs779053029	snp	C/T	3.53363e-05	0.0042032	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948169	CAAGGATCTCATCCA[C/T]GATGTCTCTTTCGAC	81929
rs779062613	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12985113	TTTTTGGTCACTGCC[C/T]GTACTGCATATTTTC	81929
rs779070026	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12983969	ATTGTAGTTTAAGGA[C/T]ATGGGTACAGATTTG	81929
rs779160037	snp	A/G			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949177	CGGCCTACAAGCAGA[A/G]TTTCTAATGTGGGGA	81929
rs779189266	snp	G/T	1.65438e-05	0.00287605	intron-variant	SEH1L	GRCh38.p7	18:12971119	AATGTGTATTTCTTT[G/T]GTTATCTAAAATGTT	81929
rs779202819	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12960066	AAAAGTCTGTGTTTC[-/A]TTTGGTCTCAGGTAA	81929
rs779258003	in-del	-/G			intron-variant	SEH1L	GRCh38.p7	18:12954005	CTTATCTGCCTTAGT[-/G]TGCATTTTTAATTTT	81929
rs779410467	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12958640	ATTTCACTAAGTAAA[A/G]TGTTTTCATGGTCTG	81929
rs779443400	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12977416	GCCTTTGCATAGTTT[C/T]CTTTTATTATCACTT	81929
rs779509661	snp	C/T	4.95356e-05	0.00497648	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986982	TGCTGACACTGCCAA[C/T]CTCCAGTATCCTCAC	81929
rs779521733	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12970436	CTTCTTTTCTTTTTT[C/T]CTGAAAGAGACTCTC	81929
rs779532239	in-del	-/CTGT			intron-variant	SEH1L	GRCh38.p7	18:12958552	CTACCCCCTATTCAA[-/CTGT]CTGTCTATAAATTTG	81929
rs779564825	snp	C/T	3.62522e-05	0.00425732	missense, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986890	CCTCTGGATTCCCCA[C/T]GGGCTGGATCGAGAT	81929
rs779605618	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12957662	GATTTGTTTTTTGTA[A/G]TAGATAATCATGCAC	81929
rs779706273	snp	A/G	3.29576e-05	0.00405928	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982566	GTTTGAAATCCATAT[A/G]GTGGCTCAGTTCGAT	81929
rs779759540	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12951201	GCGATACTCTATTTT[C/G]GCTCATACTGTAAGC	81929
rs779792643	snp	C/T	0.00409797	0.0450798	intron-variant	SEH1L	GRCh38.p7	18:12955446	TGTTCTTTTCTTTTT[C/T]TTTTTTGATTCCCCA	81929
rs779852409	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12975190	AGAGATGGGGTTTCT[C/G]CATGTTGGTCAGGCT	81929
rs779982065	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12951563	GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA	81929
rs780035511	snp	A/G	1.78627e-05	0.00298849	intron-variant	SEH1L	GRCh38.p7	18:12951945	TAAAAATACAGAAAT[A/G]TTTACTGTTTATTTT	81929
rs780038355	snp	C/T	5.02197e-05	0.00501072	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948081	CCGCCGCCGCTGCCG[C/T]CGCCACTGTCCTCTT	81929
rs780090956	snp	A/C	3.32325e-05	0.00407617	intron-variant	SEH1L	GRCh38.p7	18:12982691	GTAAGAGTTCAGTGA[A/C]GGGGTAATTGTTGGT	81929
rs780133963	snp	A/G			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949219	ATTTAGGAACCTCCC[A/G]GATGTGTTGCAGGAT	81929
rs780150803	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12978819	ATTGCATTCGCTCCA[A/G]ATTTGGGAAGATCTT	81929
rs780169677	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12947257	TTTCCCTACCCCCGT[A/G]GTGGCTCCTAGCACC	81929
rs780201740	snp	A/G	1.71402e-05	0.00292742	intron-variant	SEH1L	GRCh38.p7	18:12978710	TGTGGATTTTTGCAC[A/G]TTTTATTTCTAAAAT	81929
rs780207662	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12975211	TGGTCAGGCTGGTCT[C/T]GAACTGTCGACCTCA	81929
rs780277719	snp	C/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963230	CTCCCAAGCACATGG[C/G]TCTTATGTTAGCAAC	81929
rs780312189	in-del	-/A	6.86099e-05	0.00585664	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12985296	TTTGCTGCTTGTTGC[-/A]ATGCACACAGGAATG	81929
rs780470423	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12970229	AGGCAAAGGAAATTA[C/T]GTTAATTAGGCATAG	81929
rs780513793	in-del	-/TTG			intron-variant	SEH1L	GRCh38.p7	18:12952161	CTTTACATATTTTAA[-/TTG]TTGTGATGTTTCATA	81929
rs780516553	snp	A/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946909	TGGCCAAAATCCAAA[A/G]GGCAAGTCCCTTCTG	81929
rs780666760	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12957310	GCACATGCCTGTAAT[C/G]CCAGCTACTCAGGAG	81929
rs780677589	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12983498	ATGCTCCCCAGCAGG[A/G]TGCCTAACTTGATTT	81929
rs780711888	snp	A/C	0.000197664	0.00993947	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12963187	ACTCTGGTGGATAGC[A/C]GAACATCTGTTACTG	81929
rs780763157	snp	A/G	1.67052e-05	0.00289004	intron-variant	SEH1L	GRCh38.p7	18:12955647	GGGGACCGGGAAGAC[A/G]TGAGCAGCCAAGGAG	81929
rs780763370	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12985007	TTTAAGTACATGCAT[A/C]AAAACAATTTCAGGT	81929
rs780766927	snp	G/T	1.66885e-05	0.00288859	intron-variant, utr-variant-3-prime, nc-transcript-variant	SEH1L	GRCh38.p7	18:12986833	TTTTTGTTTTGTTTG[G/T]TGTTTTGTTCCTGTC	81929
rs780801859	in-del	-/TAC	1.6623e-05	0.00288292	intron-variant	SEH1L	GRCh38.p7	18:12978925	TTATGAATTTGAAAA[-/TAC]TCTTGCCTTCTGATT	81929
rs780837703	snp	C/T	1.65089e-05	0.00287301	synonymous-codon, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982666	GATGGGTGTGTAAGA[C/T]TGTGGAAAGGTAAGA	81929
rs780856322	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12963594	TTTTGGATGTTTTCT[A/G]TGCATATGCAAATAA	81929
rs780860581	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12968585	TACTGATGGTGATAC[A/G]GACTCTTTTTTCCTT	81929
rs780865615	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12975435	GGATGGTCACCTGCT[-/A]AGAGATGGCAGCACA	81929
rs780933316	snp	C/T			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946481	AACTAAAGTCTATTT[C/T]AAAAAATCCACTGTT	81929
rs781026373	snp	C/G/T	6.61336e-05	0.00575005	intron-variant	SEH1L	GRCh38.p7	18:12951842	AAAATATCTGCCTTT[C/G/T]ATTTTCTTATAGGTC	81929
rs781079210	snp	C/G	1.64977e-05	0.00287203	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12982543	ACTTCCTCTGGTGGG[C/G]CAACAAAGTTTGAAA	81929
rs781169276	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	SEH1L	GRCh38.p7	18:12971203	GTGATGACAGTAGCC[C/T]CAACGCAATGGCCAA	81929
rs781251838	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12962199	CCAGGAGTTTGAGAC[C/T]CATCTGGGCAACATA	81929
rs781282289	in-del	-/A			intron-variant	SEH1L	GRCh38.p7	18:12952054	CGCTATTAAAGTAAC[-/A]ACTGTGTTTCTCAGA	81929
rs781295574	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12978105	AATGCTGGGATTACA[A/G]GTGTGAGCCACTGTG	81929
rs781318120	snp	C/T	0.00077295	0.0196438	intron-variant	SEH1L	GRCh38.p7	18:12978701	GCAGTGATGTGTGGA[C/T]TTTTGCACATTTTAT	81929
rs781344463	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12959399	GTTGCCCAGGCTGGT[C/G]TTGAACTCCTGGGTT	81929
rs781363677	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12972220	TGAGAAGTGGTATCA[A/G]TAGGATCTGGTGATT	81929
rs781443645	snp	A/C	0.000199629	0.00998872	missense, upstream-variant-2KB, nc-transcript-variant	SEH1L	GRCh38.p7	18:12948137	ATGTTTGTGGCTCGC[A/C]GCATCGCGGCGGACC	81929
rs781453243	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12973849	CTGTCATGCTTAGTA[C/G]ACTGGTGATAGCTCC	81929
rs781484328	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12965228	CGTATTAGCCAGGAT[A/G]GTCTCGATCTCCTGA	81929
rs781535026	snp	A/T	3.47325e-05	0.00416714	intron-variant	SEH1L	GRCh38.p7	18:12984268	TTAAGGTGGATTATT[A/T]CATGGATTATAAGAT	81929
rs781553400	snp	A/T			intron-variant	SEH1L	GRCh38.p7	18:12967500	AGGCGAACTGACTAA[A/T]CTGTGTAAAGGACAT	81929
rs781633662	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12983254	GATTTGTGCACCACC[A/G]TAGAATGGTGTCCCA	81929
rs781655894	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12982104	CTCCTGGCCTCAAGT[C/G]ATCTGTCCACCTTGG	81929
rs781666299	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12966677	AAAGTGCTGAGATTA[C/T]AGGCATGAGCCACTG	81929
rs781695128	snp	C/G			upstream-variant-2KB	SEH1L	GRCh38.p7	18:12946046	ACTATAAGGAAAGAA[C/G]CCAATCTGAAAAGGC	81929
rs796071594	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12972309	GGTTCTGGCTTAAGA[C/G]TTCAGTGTGTAATTT	81929
rs796087569	snp	A/C			intron-variant	SEH1L	GRCh38.p7	18:12981112	TCTCAGACAGGGCGG[A/C]CGGGCAGAGATGCTC	81929
rs796090338	in-del	-/T			intron-variant	SEH1L	GRCh38.p7	18:12955452	TTTCTTTTTTTTTTT[-/T]GATTCCCCAGACACA	81929
rs796143737	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12979691	GGGTGGCTGGCTGGG[C/T]GGGGGGCTGACCCCC	81929
rs796154235	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12964144	ATAGAGCATGACTAT[A/G]TGAATATTACCATAG	81929
rs796171550	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12979740	GGGCGGCTGGCCGGG[C/T]GGGGGGCTGACCCCC	81929
rs796219313	snp	G/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949454	ACCGTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	81929
rs796293158	in-del	-/CCCCCC			intron-variant	SEH1L	GRCh38.p7	18:12969212	AAAACTCTGTACCCG[-/CCCCCC]CCCCCCCCCCCACCT	81929
rs796309371	in-del	-/AA			intron-variant	SEH1L	GRCh38.p7	18:12962378	GACCCTGTCCCTAAG[-/AA]AAAAAAAAAAATAAT	81929
rs796354257	snp	C/G			intron-variant	SEH1L	GRCh38.p7	18:12975449	CTAGAGATGGCAGCA[C/G]ATACCTGCCTGGTAG	81929
rs796376250	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12980170	CGGCCGGGCAGAGGC[A/G]CCCCTCACCTCCCGG	81929
rs796403440	in-del	-/AA			intron-variant	SEH1L	GRCh38.p7	18:12956455	TGTGTCTGGGGAATC[-/AA]AAAAAAAAAAAGAAA	81929
rs796443639	snp	G/T			intron-variant, upstream-variant-2KB	SEH1L	GRCh38.p7	18:12949458	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTGAG	81929
rs796549692	in-del	-/CCCCC			intron-variant	SEH1L	GRCh38.p7	18:12969212	AAAACTCTGTACCCG[-/CCCCC]CCCCCCCCCCCCACC	81929
rs796645007	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12960819	AGCAGTGGCAAATCC[A/G]TATGGGTCTGCAGCA	81929
rs796778825	snp	C/T			intron-variant	SEH1L	GRCh38.p7	18:12980473	CGGGCGGGGGGCTGA[C/T]CCCCCAACCTCCCTC	81929
rs796833401	in-del	-/AT			intron-variant	SEH1L	GRCh38.p7	18:12982795	TACTTTTAATGTCAT[-/AT]TAATTTATGTTATTT	81929
rs796987434	snp	A/G			intron-variant	SEH1L	GRCh38.p7	18:12956468	TCAAAAAAAAAAAAA[A/G]AAAAGAACAGATACT	81929

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