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

USP42

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs149978322	snp	G/T	0.00953873	0.0683987	intron-variant	USP42	GRCh38.p7	7:6128809	TCATTTTGCTTTACT[G/T]GAGTCTTTCTTTCTT	84132
rs150071702	snp	A/G	0.0279526	0.114869	intron-variant	USP42	GRCh38.p7	7:6089146	ACCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC	84132
rs150101632	snp	C/T	0.0232847	0.105357	intron-variant	USP42	GRCh38.p7	7:6098106	AGACGGGTTTCACCA[C/T]GTTGGCCAGGATGGT	84132
rs150200970	snp	A/G	0	0	intron-variant	USP42	GRCh38.p7	7:6146792	GGTGCAGCTGCAGGG[A/G]GAGGTGGTGGCTGAC	84132
rs150211756	snp	A/G	0.00993419	0.0697739	intron-variant	USP42	GRCh38.p7	7:6157541	TAGCCGGGACTACAG[A/G]CGCCCGCCACCACGC	84132
rs150242906	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103859	AGGAATCTTAGACCT[C/G]CCCGGGCAACAGTAA	84132
rs150249672	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6116255	CTCTTGTCACTGCCC[A/G]CAACCTCCTGGAATT	84132
rs150312213	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6144870	GTCAGATTCTGTCTC[-/A]AAAAAAAAAAAATTA	84132
rs150368729	snp	C/T	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6126680	CTGCGGTAAACACAT[C/T]TAGGTTGTTTCTAGT	84132
rs150402889	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6091680	ATCATTATGTTAGCA[C/T]ACACACACACACACA	84132
rs150406216	snp	A/C	0.0103295	0.0711199	intron-variant	USP42	GRCh38.p7	7:6083376	TTCTCCTGCCTCAGC[A/C]TCTCAAGTAGCTGGA	84132
rs150464765	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6149232	TCCTTCCTGGCACTC[G/T]GCATCAGCGAGCTCC	84132
rs150484876	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141838	GATATATGTAAAATC[C/G]TTTCCTTTTGAATGC	84132
rs150526976	snp	C/T	0.00557542	0.0525036	intron-variant	USP42	GRCh38.p7	7:6124102	GCTGGTCTTGAAATC[C/T]TAACCTCAGGTCATC	84132
rs150571105	snp	A/C	0.0178098	0.0926698	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079994	TTTGGGAGGCCAAGG[A/C]GGGTGGATCACGAGG	84132
rs150574619	snp	G/T	0.0182019	0.0936463	intron-variant	USP42	GRCh38.p7	7:6150956	GGGATGTGGTTGTCA[G/T]GCCAGCACCACAGTG	84132
rs150612440	in-del	-/GGGGG			intron-variant	USP42	GRCh38.p7	7:6150339	AGCCTCGTTTGTGGC[-/GGGGG]GGTTCCCTTGGCTGG	84132
rs150613268	snp	A/G	0.0182019	0.0936463	intron-variant	USP42	GRCh38.p7	7:6108318	AGAGGCAGGAGGATC[A/G]TTTGAGGCCAGGAGT	84132
rs150641357	snp	A/G	0.00953873	0.0683987	intron-variant	USP42	GRCh38.p7	7:6138204	CACATGTAAAATTCA[A/G]TATATATGTTTTAGT	84132
rs150685483	snp	A/G	0.0700422	0.173537	intron-variant	USP42	GRCh38.p7	7:6094849	CTGGAGTACAGTGAC[A/G]CAATCTCGGCTCATT	84132
rs150719532	in-del	-/TTATTTAT			intron-variant	USP42	GRCh38.p7	7:6083224	GCCACCGCACCCAGC[-/TTATTTAT]TTATTTATTTATTTA	84132
rs150726419	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6121264	CTTTTACCATTAAGT[A/G]TGGTGTTGTAGGTTT	84132
rs150736027	snp	G/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6158589	GTGAGCCCCATGGGG[G/T]ACATTTGCCCATGGA	84132
rs150769604	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077319	CTCTTACATTGTACT[A/G]AGGTTGGTCTGTGTG	84132
rs150896319	snp	C/T	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6127855	TTGGGGGGATTAACA[C/T]CTTTACTATGTCCCT	84132
rs150959853	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6078907	GTAGATCCTGTCAAT[C/T]AAGAGCGAATTGCCC	84132
rs150994876	snp	C/T	0.0185938	0.0946107	intron-variant	USP42	GRCh38.p7	7:6091523	TTGAGCCGCCATGCC[C/T]AGTGCCATACATAGC	84132
rs151011297	snp	C/T	0.000274408	0.0117102	synonymous-codon	USP42	GRCh38.p7	7:6144178	TTTTGCAAATTTTAC[C/T]GGTGGAAAAATTGCT	84132
rs151054692	snp	C/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6100765	CCCACCTCCCAGGTT[C/G]CAGCAATTCTCCTGC	84132
rs151101430	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6152260	CGGTGCCAGGCGCGG[G/T]TTCATCATCAGGAAG	84132
rs151218704	snp	A/G	0	0	intron-variant	USP42	GRCh38.p7	7:6096975	GTCATCCATGCTGGA[A/G]TGCTGTGGCATGATC	84132
rs151312630	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6119104	CCTATAGTCCTAGTT[A/G]CTTCGGAGGCTGAGG	84132
rs180678645	snp	A/C	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6091337	TCAAGCGATCCTCCC[A/C]CCTCCGCCTCCCTCA	84132
rs180694308	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122007	TTTTTAATGTTACTG[A/G]TCTTCTCAAAGAACG	84132
rs180703163	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137188	TAATTATACAGTAAC[A/G]AACTGTAATCTTTTT	84132
rs180721073	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6084184	GGCATGAGCCACCAC[A/G]CCCAGCTAATTTTTG	84132
rs180722618	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099560	AGTATGTTGGGCAGG[C/T]GGGTCTCAAACTCCT	84132
rs180731446	snp	A/G	0.0263992	0.111815	intron-variant	USP42	GRCh38.p7	7:6129426	GCCAGGCATGGTGGC[A/G]GGCGCCTGTAATCCC	84132
rs180734426	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6153652	AATAAAATAAAGAGA[C/T]GAAATAGCAAATGAA	84132
rs180736755	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116344	ATCAGTTAAAGCTTA[C/T]TAAAATGTCTTTAAT	84132
rs180739822	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6147021	TTCACTCACTCACTC[A/G]CTCCATTTTTGGAAA	84132
rs180935914	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094874	CTCATTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	84132
rs180944042	snp	C/T	0.0185938	0.0946107	intron-variant	USP42	GRCh38.p7	7:6087094	TGGAGTGCAGTGGTG[C/T]GATCTCAGCCCACTG	84132
rs180951558	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6112065	AAAATGGTTGTCTTT[G/T]GACAAATGAGCTTTA	84132
rs180965265	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6126410	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	84132
rs180970720	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157861	CTGCCCTGTGGGGCT[G/T]TGTCTCCGTCCTGTG	84132
rs180975177	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6144611	GTGGTGGCTCACGCC[C/T]GTAATCCCAGCACTT	84132
rs180981494	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120052	CTCACTGCAACCTAC[A/G]CCCCCGGGTTCACGC	84132
rs180986269	snp	C/T	0.00517822	0.0506191	intron-variant	USP42	GRCh38.p7	7:6150910	TCCGTCCGTCCACAA[C/T]AGGGATGCCTTCTGA	84132
rs180992406	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103365	AACATGGTGAAACTC[C/T]GTCTCTACAAAATAC	84132
rs181012909	snp	C/G	0.0142736	0.0832652	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079988	CAGCACTTTGGGAGG[C/G]CAAGGCGGGTGGATC	84132
rs181016419	snp	C/T	0.00557542	0.0525036	intron-variant	USP42	GRCh38.p7	7:6132398	AGTTTCACTCCGTGG[C/T]CCAGGCTGGAGTGCA	84132
rs181166382	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6115928	ACATAGTAAGACCCC[A/G]TCTCTACTAAAAATA	84132
rs181174904	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099324	GGTTCAAGAGATTCT[C/G]CTGCCTTAGCCTCCC	84132
rs181180670	snp	C/T	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6129231	TACTTCCCTATGTCC[C/T]TTACTCTCCACTAGT	84132
rs181194900	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091971	CTTAGTCCTCAAGGA[C/T]GTATTTTTTCTTCTT	84132
rs181195160	snp	A/C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161992	TATATTTACCGCAAA[A/C/T]AGAAATATTTTCTAA	84132
rs181196727	snp	A/G	0.00155978	0.0278829	synonymous-codon	USP42	GRCh38.p7	7:6146189	GAATGACTCCATTGT[A/G]TCTACCAGTGATATT	84132
rs181249104	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6083491	AAACTCCTGACCTCA[A/G]GTAATCTGCCCGCCT	84132
rs181277472	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108366	AACGTAGTGAGACCC[G/T]GTCTCTACAAAAAAG	84132
rs181286342	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138411	ATGGATTCTGTATTA[C/T]AGAGATGTAGCACCA	84132
rs181339046	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6122839	AAACTCCTGGCTTCA[A/G]GACAGTTGTCTTGAA	84132
rs181371881	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6079329	CCGGCGGGGTGGCAC[A/G]TGCCTGTAATCCCAG	84132
rs181385153	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6094539	GGATGGAGTGGGTAG[C/T]GGTGGAATTAAGCTG	84132
rs181389459	snp	A/G	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6154703	GCCGGGAGAAGTTCT[A/G]CCCCGACAGGCCGCG	84132
rs181402625	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6111433	GTAAATGCTGCTGGG[A/G]CTTGGTGGTTTCAGA	84132
rs181496799	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133216	GCTCAGTCAGGGTAC[A/G]AAACCATGCCTCTTC	84132
rs181502915	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6151673	GTCTCAAACTCCTGA[C/T]CTCAACTCATCCACC	84132
rs181529440	snp	C/T	0.00953873	0.0683987	intron-variant	USP42	GRCh38.p7	7:6157460	GGAGTGCAGTGGCGG[C/T]GATCTCAGCTCACTG	84132
rs181669032	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120640	CCAGGCTGGAGTGCA[A/G]TGGCACAATCTCGGC	84132
rs181701655	snp	A/G/T	0.00987637	0.0695952	missense	USP42	GRCh38.p7	7:6154240	GGCGCACCCGAGGCC[A/G/T]CAGAGCGGCCGCCAG	84132
rs181705885	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137952	CCAAAGTGTTGGAAT[A/T]ACAGGTGTGAGCCAC	84132
rs181808186	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091897	CTCAATCGGCATTTC[C/T]TCCTGAAATGCTGGC	84132
rs181848641	snp	G/T	0.0123036	0.0774623	intron-variant	USP42	GRCh38.p7	7:6122287	TGTGTCAGTTTTTTT[G/T]TTTTTTTTTTTAAAG	84132
rs181892321	snp	A/G	0.00517822	0.0506191	intron-variant	USP42	GRCh38.p7	7:6087311	GCTGGGATTACAGAC[A/G]TGAGCCACCGCACCT	84132
rs181907834	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120514	TCCCAAAGTGCTGGG[A/T]TTACAGGCATGAGAC	84132
rs181915520	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103796	CAGCGGCTCACGCCT[A/G]TAATCCCAACACTTT	84132
rs181916807	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6132759	TCACTGCAACCTCCG[C/T]CTCCCGGGTTCACGC	84132
rs181928850	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151113	GACAGTAAAAATATG[A/G]TATAAGAGGAAAACT	84132
rs182026911	snp	A/G	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6079081	ATCTTGAATTTTATT[A/G]AAGTGAAACACTTTA	84132
rs182047798	snp	C/G/T	5.91932e-05	0.00543995	intron-variant	USP42	GRCh38.p7	7:6111091	TTGCTTTTCTCACCT[C/G/T]ATGAAACAAATACAT	84132
rs182081008	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107637	TGGTCTTGAACTCCT[C/G]ATTTCAGGTGATCTG	84132
rs182099345	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109143	CAGAGAAAGTAAAGT[C/T]TAAACTGAGAAGTGG	84132
rs182102031	snp	G/T	0.00716266	0.059414	intron-variant	USP42	GRCh38.p7	7:6092131	TCCTCTTCCTTCTTC[G/T]TCTTCTTCTTCCTCT	84132
rs182107253	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140750	TCATTACACTTTTCA[C/G]CCATATTATGAGTAG	84132
rs182110664	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6123391	AAATTGGGCTGGGTG[C/T]GGTGGCTCACGCCTG	84132
rs182111048	snp	A/C	0.000798403	0.0199641	synonymous-codon	USP42	GRCh38.p7	7:6155187	CAAACACCGAGACCG[A/C]GACTCCAGGTGAGCC	84132
rs182311908	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6088573	CCTACTCTTATTACT[C/T]TTATTGACAATCCTT	84132
rs182357017	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094055	CCGGCTAATTTTTTT[G/T]GTATTTTTAGTAGAG	84132
rs182429882	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113781	TGCCTGCCACCACAC[C/T]TGGCTAATTTTTTGT	84132
rs182448175	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100977	CTGGCTGGTACCCAC[G/T]GTCTTAAACCAGGAT	84132
rs182453405	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6127860	GGGATTAACATCTTT[A/T]CTATGTCCCTGAAGT	84132
rs182471448	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159853	GCCCGGTCCCCAGCA[C/T]AGGCACCTCACTCAG	84132
rs182474509	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6145262	CTTGAACCCGGGAGG[C/T]GGAGCTTCCAGTGAG	84132
rs182480694	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130795	AGGCTCAGGAAGACA[A/G]AGATTTTATGCTCAC	84132
rs182670480	snp	C/T	0.0119091	0.0762411	intron-variant	USP42	GRCh38.p7	7:6085803	TATTTTTAGTAGAGA[C/T]GGGATCTCACCATGT	84132
rs182689813	snp	A/G	0.0252325	0.109451	intron-variant	USP42	GRCh38.p7	7:6130332	TGTCCCTGCTGGGTG[A/G]AAGTGGAAGTTCCTG	84132
rs182697924	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6117329	TTATCTCGCTTCTTT[C/G]ACTCAGCATAATCCT	84132
rs182711617	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6148492	ACTTGGAGATTCTTT[A/C]ATTCCTGTCGGATTG	84132
rs182712545	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121082	CGCAACTATGTGATA[C/T]GTGAATAAAGATAAT	84132
rs182713753	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6117639	TTCCAGAAGGGATTG[C/T]AGTGTTTTATAGTCC	84132
rs182723499	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151853	GCATCACCACACTCA[C/T]GAGGCACGCGTTGCC	84132
rs182728026	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098192	ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCCATGT	84132
rs182733871	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6148857	TCTGCTCCAGAGTGA[C/T]ATCAGGACTCTGGCA	84132
rs182898610	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080961	ATTTTAAACACATTA[C/T]CCTGTGTCTCAGTTT	84132
rs182916509	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096286	GAGACCAGCTTATTA[C/T]TTGGTGCCAGTAAGA	84132
rs182932819	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6112943	GAGTCTCGCTCTGTC[A/G]CCCATTCTGGAATGC	84132
rs182945105	snp	C/T	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6127694	AGTAAGTCTTGTCAT[C/T]GGTTAGAATGATTCC	84132
rs182974213	snp	C/G	0.0189856	0.0955633	intron-variant	USP42	GRCh38.p7	7:6105618	CCACCTGGCTGCTCC[C/G]TGGAGAGTCCGAGGT	84132
rs182979141	snp	C/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6085280	GCGCACCACCATGCC[C/T]GACTAATTTTTTTTT	84132
rs183010784	snp	A/G	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6133763	GGGCTCAAGTGGTCC[A/G]CCTGCCTCAGCCTCC	84132
rs183043633	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141702	TAGCTGGGACTACAG[C/T]GACTGTGCCCAGCCT	84132
rs183121898	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6085008	ACAGGTGCGAGCCAC[C/T]GCACCCAGCCAAGGA	84132
rs183135051	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6100361	TAATACGGAGTTTCG[C/T]TCTTGTTGCCCAGGC	84132
rs183145351	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117057	AATTGATATATACCA[A/G]ATTACACATATTTAA	84132
rs183165609	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6129677	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC	84132
rs183247815	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6121534	GGATATGTTTTCTTC[A/G]CATCTGTTTCCTGGA	84132
rs183262779	snp	C/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6089280	GTTCATCTTGAACTC[C/G]TGATCTTAGGTGATA	84132
rs183264055	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106049	GTTGTACATTTTAAA[C/T]CTAATTCTTTTTACT	84132
rs183267400	snp	A/G	0.00517822	0.0506191	intron-variant	USP42	GRCh38.p7	7:6135579	TGGCTTGGACCCGGG[A/G]AGGCCGAGGTTGCAG	84132
rs183282849	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152076	GAATGTGAATGTAAC[A/G]TTGGTCAGGAGTGAG	84132
rs183283794	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6100611	CTGGGATTACAGGCG[G/T]GAGCCACTGTGCCTG	84132
rs183295465	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104239	AGGCGCGCGCCACCA[C/G]GCCCGGCTAATTTTT	84132
rs183323569	snp	C/T	3.29245e-05	0.00405724	intron-variant	USP42	GRCh38.p7	7:6156705	TCCAGGGTCTGCTGC[C/T]GGTGGTTTTGTGTTT	84132
rs183493666	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6088400	AGCTGGGATTAAAGG[C/T]ACCCGCCACCATGCC	84132
rs183568277	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092821	CCTCAGAAGATTAAA[C/T]ATATCCCTCCTTGAA	84132
rs183607182	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6155701	ACACCTTCGTTTCCT[C/T]GGCCTTTGTTTTTGT	84132
rs183684590	snp	C/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6093965	CGCGATGTGGGCTCA[C/G]TGCAACCTCCACCTC	84132
rs183697137	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6110932	GATTGTTGACATTCA[C/G]ATTATCATGATGCTA	84132
rs183710730	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124091	ATGTTGGCCAGGCTG[G/T]TCTTGAAATCTTAAC	84132
rs183717405	snp	A/G	0.00579902	0.0535339	synonymous-codon	USP42	GRCh38.p7	7:6156961	TCTCTCTGGTGGCCC[A/G]CCTCTGGAAGGCGTC	84132
rs183722328	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142297	TCTCGGCTCACTGCA[A/G]CCTCCACCTCCTGGG	84132
rs183804685	snp	C/T	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6109857	AGGTACGTGCCACCA[C/T]GCCCGGCTAATTTTT	84132
rs183806281	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6076835	GCCCGCCTTGGTCTC[C/T]CAAAGTGCTGGGATT	84132
rs183827782	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6141263	GCTGGCATGCAGTGG[C/T]GTGATCTCGGCTCAC	84132
rs183889223	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6112542	TTCGTTAAAACTCAT[C/G]CAGATAAATGAGACA	84132
rs183908510	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6144818	GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCACTG	84132
rs183932890	snp	A/C	0.0228947	0.104514	intron-variant	USP42	GRCh38.p7	7:6090037	AGGCGCAGTGGCTCA[A/C]GCCTGTAATCCCAGC	84132
rs183961755	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107193	AATTGTGCTTTCGTT[A/G]AATTTTTTTTCACTT	84132
rs184048123	snp	C/T	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6095364	CCCAGCATATAATTA[C/T]GGAGTAAATTAAATG	84132
rs184056767	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6127023	GTTCATTTTACCTGT[A/G]CTGATAGGTGTGTAG	84132
rs184083812	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158727	TTCCCATTTCAGCGA[A/T]TCGGGGAAGGAGATT	84132
rs184181350	snp	C/T	0.00716266	0.059414	upstream-variant-2KB	USP42	GRCh38.p7	7:6078089	GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCATTG	84132
rs184183758	snp	C/T	0.0107246	0.0724382	intron-variant	USP42	GRCh38.p7	7:6093430	AACTGGGACTACAGG[C/T]ATGCACCACCATGCT	84132
rs184196761	snp	G/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077542	CTTCATCCCCAGTAG[G/T]CCCTTGAAATGTCCT	84132
rs184207206	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6110039	GGGTCTCACCATGTT[A/G]GCCAGGCTGGTCTCA	84132
rs184249594	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098838	GGCATGAGCCACCAT[A/G]CCCTGCCAAGAATGC	84132
rs184263813	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6083321	AGTGCAGTGGTGCTA[C/T]CTTGGCTCACTGCAA	84132
rs184265074	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6115742	GTATTTAAAAAGAAA[C/T]ATTTTATCAGCTTTT	84132
rs184265126	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153323	AAAAAAATAGAGGAA[C/T]TGGAAGAACTAGAGG	84132
rs184266411	snp	C/G	0.00597247	0.0543191	intron-variant	USP42	GRCh38.p7	7:6132551	TTTAGTAGAGACAGG[C/G]TTTCACCATGTTAGC	84132
rs184274961	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6145791	AATATTTCTCTTGGC[C/T]GGGCGCAGTGGCTTA	84132
rs184280950	snp	A/G	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6128685	TAAGACTTAAGGCTT[A/G]TTCTGCCATTTAATG	84132
rs184477737	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118640	TTTTGGGTCAGTGGT[C/G]CATTTTGAGTTAATT	84132
rs184481430	snp	C/T	0.0425829	0.139564	intron-variant	USP42	GRCh38.p7	7:6086272	GTGTAGTGGCGCGAT[C/T]TCAGTTCACTGCAAG	84132
rs184487934	snp	A/G	0.0704125	0.17392	intron-variant	USP42	GRCh38.p7	7:6101895	TCCAGCCTGACCAAC[A/G]TGGTGAAACCCCATC	84132
rs184498417	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131617	GGAGAGAGTGGGAGC[A/G]GGATTTTGCTGGGCT	84132
rs184511421	snp	A/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6149420	GAAAGTATGCGCGGG[A/T]AGGAGGGATTGAGAA	84132
rs184529145	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6121880	TGCCCAGGGTAGTCT[C/T]GAACTCCTGGCTTCA	84132
rs184611416	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081265	AGCGTTCAGCGGCTA[A/T]CGGAGGTGAGCTGGA	84132
rs184679746	snp	G/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6136651	ATTAGTTTCAGTTTG[G/T]TGAATGAATACTTTA	84132
rs184823998	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086608	ACCCCCCTCAACCTC[C/T]CAAAGTTCTGGGATT	84132
rs184837300	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119030	GACCAGCCTGGGCAA[C/T]ATGTCAAGACCCTGT	84132
rs184911894	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6123739	TATAGTCTTAGCTAC[A/T]CGGGAGGCCGAGGTA	84132
rs184928866	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6102356	TGATCTTGTGATCTG[C/T]CCGCCTCGGCTTCCC	84132
rs184939307	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131924	CTCATGGGGTGTAGA[A/G]TTCTATGTTAACATT	84132
rs184947446	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091515	TAACAGGCTTGAGCC[A/G]CCATGCCCAGTGCCA	84132
rs184969254	snp	G/T	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6107495	GCTCACCACAACCTC[G/T]GCCTCCTGGGTTCAA	84132
rs184980412	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6137191	TTATACAGTAACAAA[C/G]TGTAATCTTTTTGCC	84132
rs184985312	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122092	TGATGTTTGTTGTTA[C/T]TGTCATTATTCCATT	84132
rs184987363	snp	A/C	0.00127705	0.0252367	synonymous-codon	USP42	GRCh38.p7	7:6153855	GCCAGATGCGGCCGC[A/C]GGCCTCAGCAGCACC	84132
rs185040818	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6126436	ACTACAGGTGCCCAC[C/G]ACCACGCCTGGCTAA	84132
rs185049048	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6157952	CCGGTGACCGCTCAC[C/T]CTCGAGAGGAGCTGT	84132
rs185050936	snp	A/G	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6144680	TTTGAGACCACTCTG[A/G]CGAACGTGGCAAAGC	84132
rs185062995	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106473	ACCATATAAGAGACT[A/G]GGAATTTTAAAGCTT	84132
rs185093481	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135813	GGTTGTATTTTGCTA[A/C]TTTGGAGGATTATCA	84132
rs185110158	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6161076	TGAAGATGTATTTTA[C/T]AGACAAGTTCTGTTT	84132
rs185182985	snp	G/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6089702	CACGCCTGGCTAATT[G/T]TTTTGTATTTAGTAG	84132
rs185191637	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121849	TTATTTTTGTAGAGA[C/T]GAGGTCTCACTATGT	84132
rs185216393	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087238	CGTTCACCATGTTGG[C/T]CAGGCTGGTCTGGAA	84132
rs185269637	snp	A/G	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6129372	ACCAGCCTGGCCAAC[A/G]TGGCGAAACCCCATC	84132
rs185282746	snp	C/T	0.00716266	0.059414	intron-variant	USP42	GRCh38.p7	7:6122856	ACAGTTGTCTTGAAC[C/T]GCTGGCGCCCAGGCT	84132
rs185290636	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146349	TTTTAAAAAAAAAAA[A/C]AAACCCAGCAGCTTA	84132
rs185290884	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6108451	TATTATCCCTACTTC[A/G]TAGCATGGGTAGTAC	84132
rs185350633	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6094276	CCTCCTGGGCTCAAG[C/T]GATCCTCCCACCTCA	84132
rs185361126	snp	C/G	0.00953873	0.0683987	intron-variant	USP42	GRCh38.p7	7:6125955	TTACTGAACCTCCCC[C/G]AGTGATAACACTGTA	84132
rs185366715	snp	C/T	0.00676609	0.0577691	intron-variant	USP42	GRCh38.p7	7:6092085	TTCTTCCTCTTCCTC[C/T]TCTTCTTCTTCCTCC	84132
rs185385071	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157253	AGTTAAGCCCTTAGC[A/G]TTTATTGAAGGCCTA	84132
rs185444613	snp	C/T	0.0130921	0.0798413	intron-variant	USP42	GRCh38.p7	7:6079196	AAGCACGGGGGCTCA[C/T]ACCTGTAATCCCAGA	84132
rs185499132	snp	A/G	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6143182	CCGGAGTGTCTTGAT[A/G]TGTGTGTTTCTGCAA	84132
rs185507577	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079389	CTTGAACCCCGGAGG[A/C]GGAGCTTGCAGTGAG	84132
rs185525680	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094674	TGATGGAGACACCAG[C/T]CTTGCATCCTTTAAC	84132
rs185540174	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6111505	AGCAGAGTTGTATTA[C/G]TTGATGGGCTTTGTT	84132
rs185552720	snp	C/T	0.000458072	0.015127	intron-variant	USP42	GRCh38.p7	7:6144231	AATCATGTTTTATGT[C/T]GAGCCTTTCGAAGCT	84132
rs185557040	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6126371	CTCACTGCAGGCTTC[A/G]CCTCCTGGCTTCACG	84132
rs185566011	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6082585	TAAGGAGACTGCGTC[C/T]CTATTTTCTTTCTTT	84132
rs185606553	snp	A/G	1.65647e-05	0.00287786	synonymous-codon	USP42	GRCh38.p7	7:6145575	TCAACCCAACGGAGA[A/G]CCAATTGTCTACGTC	84132
rs185718916	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098637	GCTCACTGCAACCTC[C/T]GCCTCCCCGGTTCAA	84132
rs185729139	snp	G/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6128164	CGCTGTGTTACCCAG[G/T]CTGGTCTCGAACTCC	84132
rs185759664	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6160597	CCAGCCCAGCTTAAA[C/T]TATAAAGATAGACAA	84132
rs185870095	snp	A/C/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103393	TACAAAAAATTAGCC[A/C/G]GGCGTGGTGGCGGGC	84132
rs185892823	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6112363	CTGAGGCAGGAGAAT[C/T]GCATGAACCTGGGAG	84132
rs185897065	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080147	AGAATGGCATGAATC[C/T]GGGAGGCAGAGCTTG	84132
rs186014247	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6120066	CGCCCCCGGGTTCAC[A/G]CCATTCTTCTGCCTC	84132
rs186033322	snp	A/C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094890	CCTCCCAGGTTCAAG[A/C/T]GATTCTCCTGCCTCA	84132
rs186050989	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117285	CTAGAGTGTTGCTTA[A/T]GTGGAATTGTACAGT	84132
rs186067428	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6129958	GTTCTCAGTATGATG[A/G]GTGATTTTCAGTTGA	84132
rs186078404	snp	C/T	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6147633	AAACATGCTATTTTT[C/T]TCATCAGGTTTCCGC	84132
rs186148480	snp	G/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6099426	TCACAGTGTTAGCCA[G/T]GATTGTCTCAATCTC	84132
rs186200383	snp	A/C	0.000154835	0.00879735	synonymous-codon	USP42	GRCh38.p7	7:6155041	AAGTCCCGGAAACGG[A/C]GACACGACAGTGTGG	84132
rs186269753	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6087583	CTGAAGCAATCCACC[C/T]GCTTCGGCCTCCCAA	84132
rs186276534	snp	C/T	0.00914312	0.0669923	intron-variant	USP42	GRCh38.p7	7:6115960	AAATAAAAATTAGTC[C/T]AGCATGGCAGCACAC	84132
rs186281214	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084052	TTTGTTTTGAGACAG[A/G]GTCTCGCTCTGTCAC	84132
rs186286865	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120558	TCTTGCCTCAGCCTT[G/T]CAAAGTGTTGGGATT	84132
rs186290209	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103889	AGACCTCTGTCCCTA[C/G]AAAACAAAACTCCAC	84132
rs186291564	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133025	CACTGGTTGTAAGTA[A/G]GGGTCCTTTGTGTAG	84132
rs186301821	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6151133	AGAGGAAAACTGGCA[C/T]ACCTGCACAGGGCAC	84132
rs186384360	snp	A/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6155408	TATCTTTATTCTTCA[A/T]GGTGTCGTTAAATGC	84132
rs186403927	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6088423	ACCATGCCCAGCTAA[G/T]TTTTATATATTTTTA	84132
rs186465115	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120665	CTCGGCTCACTGCAC[C/T]CTCTGCCTTCTGGGT	84132
rs186471787	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6151732	CCAGACGTGAGCCAC[C/T]GTGCCCGGCCAGCAG	84132
rs186496647	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime	USP42	GRCh38.p7	7:6084576	TCCACATCGCTGCCC[A/G]CATCACCACGCTGCG	84132
rs186625818	snp	C/T	0.0107246	0.0724382	intron-variant	USP42	GRCh38.p7	7:6089169	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	84132
rs186627454	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121454	ATTAGCCTATAGTTT[C/G]TTATAATGCCTTTTT	84132
rs186630865	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6105758	CCAGCTTACCTGGAA[C/T]GGGGGATCCGTTGCA	84132
rs186647247	snp	C/T	0.122411	0.214991	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104889	GGCGGCCCGGAGGGG[C/T]GCGGCGGGCGCGGCG	84132
rs186661622	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6157666	AATACTTTTGCAGCG[C/T]ATACGTTACTCTCCC	84132
rs186674213	snp	C/T	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6133621	CTGGGCTCAGGTGGT[C/T]CTCCCATCCCACATC	84132
rs186679079	snp	A/C/T	0.00478244	0.0486902	intron-variant	USP42	GRCh38.p7	7:6107660	GTGATCTGCCCGCCT[A/C/T]GTCCTCCCAAAGTGC	84132
rs186710034	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6138182	AGAACATTTTTATAC[A/G]TTCATACACATGTAA	84132
rs186804390	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145301	GTGTCACTGCACTCC[A/G]GCCTGGGTGATAGAG	84132
rs186811376	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6160086	ACTGGTTTTATACCT[C/G]ACCCTTGTGGAGCTA	84132
rs186903125	snp	A/G	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6091932	ATCCTTTTTCTATTC[A/G]ATATCTGCCTGGAAA	84132
rs186906248	snp	C/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6122325	CTCACTCACTCTGTT[C/G]CCTAGGCTGGAGTGC	84132
rs186924738	snp	A/C	0.000264375	0.0114943	synonymous-codon	USP42	GRCh38.p7	7:6154317	TGAGCCTAGCCCCGG[A/C]GAGAGGGTCGAGGAC	84132
rs187003299	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6127193	TTGTTGTTGTACTGT[C/T]AAGTTTTGAGGATAT	84132
rs187008763	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093495	ACCATGTTGGCCAGG[C/G]TGGTCTCGAACTCCT	84132
rs187029035	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077692	AGGGTGAAACTCCGT[C/T]TGTACTAAAAATGCA	84132
rs187030669	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6148496	GGAGATTCTTTAATT[C/G]CTGTCGGATTGCAGG	84132
rs187039788	snp	C/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6110044	TCACCATGTTGGCCA[C/G]GCTGGTCTCAAACTC	84132
rs187043699	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158901	AGGGAGGTTGAACGT[C/G]ATCTTGTTTGCCTCG	84132
rs187047994	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6142166	GATATAATTTGGTAT[C/G]TAGATTTATAAAAGT	84132
rs187052203	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6123784	GCCAGGGAGTTGAAG[C/G]ATTATGCCACTGTAC	84132
rs187219996	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112757	AAGCTCATTAGCTGT[C/T]GTTAGTGTTAGTGTT	84132
rs187222298	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6144830	AGCCGAGATTGTGCC[A/G]CTGCACTCCAGCCTG	84132
rs187244398	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081099	TTATTTGCTCTGATC[C/T]TTTAGTTTAGGCTCC	84132
rs187253427	snp	C/T	0.0119091	0.0762411	intron-variant	USP42	GRCh38.p7	7:6097705	ATGCCATTCTCCTGC[C/T]TCAGCCTCCCGAGTT	84132
rs187264236	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6113242	GGTGTTGCAGTTTGG[A/C]TTGCTGAAGGTGTTT	84132
rs187283160	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6145045	CATGCCCTTTGAAAG[A/G]TGGCTAGGCCAGGTG	84132
rs187284269	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6127729	ACTTTATTCTTCACA[A/G]TAGTTTCGGCTATTC	84132
rs187290777	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159547	TGGCGCTGAGGGGAC[A/G]CAGGCAGAGGAGTTT	84132
rs187298242	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116664	CCAAGTAATGCTTGT[A/G]AAGAATTTGGAAAGT	84132
rs187307525	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6147066	TGAAAATCAAGAATA[C/T]TCTCAAATGTCCAAC	84132
rs187366241	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131795	TTCACAGCCTTTTAA[A/G]GTTCATTTTATACAC	84132
rs187396966	snp	A/G	4.97302e-05	0.00498624	synonymous-codon	USP42	GRCh38.p7	7:6149624	ACCATTGAAAGACAC[A/G]CCAAGCAGTTCCATG	84132
rs187470568	snp	G/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6099860	CCCAGCTACCTGGGA[G/T]GCGGAGGCAGGAGAA	84132
rs187570777	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6129655	TACCTGAGGTCAGGG[A/G]TTCAAGACCAGCCTG	84132
rs187571959	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6106240	ATAATTAAGACGAAG[A/G]TTTTGTCTTTTTAAA	84132
rs187577129	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114120	TCCTCACAAGTGTGT[A/C]CAGTGGTACCTGATA	84132
rs187582832	snp	G/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6133938	CTCTGTCGCCCAGGC[G/T]GGAGTGCAGTGGTGC	84132
rs187600321	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6135613	GCCAGGGTCACACCA[C/G]TGCACTCCAGCCTGG	84132
rs187603450	snp	A/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6121663	AAACTACATTCTTCT[A/T]TTCTTTGTTTTGTTT	84132
rs187622620	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152742	ATTAACCCCGAGGAT[A/G]TATCGAAAGCTCTGC	84132
rs187816074	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100841	TCAGCTAATTTTTTG[A/T]ATTTTTAGAAGAGAT	84132
rs187826692	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130359	CCTGCTCCCCACATG[G/T]TCTCCACGGACACTG	84132
rs187847013	snp	A/T	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6109277	TTCAGCATGGTGGGA[A/T]CGTGACGGAGAGGGT	84132
rs187851463	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6098219	ATGTAGCTTATTTCT[A/G]TTGTCAAATACCAGT	84132
rs187855236	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6101289	CTGCAGGCTCCCTAA[G/T]TCTGGAGGTCCTCAG	84132
rs187855557	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128129	ATTTTTTTATTTTTA[C/G]TTTTGTAGAGATTTG	84132
rs187859442	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6140856	TTGTCATTTCAGTAG[C/T]TGATGTTGCTGTAAT	84132
rs187861015	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151948	TGGTCTGTTGTTGAC[C/T]GTATGTATGAGGTAC	84132
rs187861495	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123441	GGCCAAGGCGAGCAG[A/T]TCACGAGCTCAGGAG	84132
rs187867805	snp	A/G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6085866	GATCTGCCCGCCTTG[A/G/T]CCTCCCAAGGTGCTG	84132
rs187870327	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156707	CAGGGTCTGCTGCTG[C/G]TGGTTTTGTGTTTTA	84132
rs188072287	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6085395	CTCCCAAAATCCTGG[A/G]ATTTTAGGCGTGGGC	84132
rs188079934	snp	C/T	0.0189856	0.0955633	intron-variant	USP42	GRCh38.p7	7:6089740	GTTTCACCATGTTGG[C/T]CAGGCTGTTCTCAAA	84132
rs188112615	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121860	GAGACGAGGTCTCAC[C/T]ATGTTGCCCAGGGTA	84132
rs188113576	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6117359	TGTCAACATTATTCC[A/G]TTTGTGCCATGTAGC	84132
rs188122562	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153351	AGGGATATCCAGAAA[C/G]AGGAAGAGCCTAGAA	84132
rs188268778	snp	C/G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091062	TTCCTTGGCCTCCTT[C/G/T]GATTGTGTTCTTCAT	84132
rs188286970	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6121920	CCCCGCTTGGCCTCC[A/G]AAAGTGCTAGGATTA	84132
rs188296250	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6107417	TCCTTTTCTTTTTTT[C/T]TTTTTTTTTGAGACG	84132
rs188300263	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136801	TAATTCTCTTTTTTC[A/G]GTTCTTCTTTTTTTT	84132
rs188342064	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109881	AATTTTTGTATTTTT[A/C]GTAGAGATGAGGTTT	84132
rs188376367	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141521	TTTAATATCTTAATA[A/C]AACTAGATTTTCTAT	84132
rs188378172	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6106956	TAACAGTAATATTTA[A/G]AAGCTTTACTGAAAG	84132
rs188408798	snp	C/T	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6136107	CCTCCCAGGTTCAAA[C/T]GATTGTCCTGTCTCA	84132
rs188452249	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144395	TATAATCTGAAATCC[A/G]AAGAGGACTTCCTGC	84132
rs188460443	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126385	CGCCTCCTGGCTTCA[C/T]GCCATTCTCCTGCCT	84132
rs188460777	snp	C/G	0.0182019	0.0936463	intron-variant	USP42	GRCh38.p7	7:6157743	CTGATTTGCTCGCTT[C/G]GTTCCTTAGAAGCGT	84132
rs188597741	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6095593	AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG	84132
rs188614641	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6093175	CCTTCCCTTCCTTCC[C/G]TCCCTCTCTCCCTTC	84132
rs188639608	snp	A/G	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6123523	AAATATTAGCCAGGC[A/G]AGGTGGCGGGCGCCT	84132
rs188668308	snp	G/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6156074	AAGCTAAATTGGTTG[G/T]TGATTGTCTTGAAAA	84132
rs188684040	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6083375	ATTCTCCTGCCTCAG[C/T]CTCTCAAGTAGCTGG	84132
rs188685969	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6115882	GGAGAAAGGATCACT[C/T]GAGCCCAAGAGTTGG	84132
rs188692203	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6099302	TCATTGCAACCTAGG[C/T]CTCCCAGGTTCAAGA	84132
rs188704099	snp	C/T	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6129098	ATTACAGGCGTGTGC[C/T]ACTGGGCCTGTAGCC	84132
rs188709640	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161836	TGCAAGAGCTCTGAC[A/G]GCCATCCACCCTCCA	84132
rs188715591	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146024	GCAAGATCACGCCAC[A/T]GCACTCCAGCCTGGG	84132
rs188873092	snp	C/T	0.00517822	0.0506191	intron-variant	USP42	GRCh38.p7	7:6092462	GGGATTACAGGCATG[C/T]GCCACCACGCCCGGC	84132
rs188880479	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080534	TTGAGGTCAGCAGTT[A/G]GAGACCAGTCTGGCC	84132
rs188892304	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6118067	GAAATTTCATTTCTT[C/T]TTTTTTCTTTTTATT	84132
rs188902056	snp	G/T	0.0103295	0.0711199	intron-variant	USP42	GRCh38.p7	7:6089559	TTTTTTTGAGATGGA[G/T]TCTCACCCTGTCTCC	84132
rs188906525	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6149030	ATCTGTTAACTGACT[G/T]TCACGCCTGCGCCTC	84132
rs188920580	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6079286	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	84132
rs188927380	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118841	CCATATCAATACGAT[C/G]TATTTCTGGACTCTA	84132
rs188931561	snp	A/G	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6086495	CAGGCGTGAGCCACC[A/G]CGCCCAGCCTAGCCG	84132
rs188933750	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6102035	CCGAGACTGTTCTAG[A/G]AGACAGGGTGACATT	84132
rs189168460	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6082695	GGCTCACTGCAACAT[A/C]TGCCTCCCAGGTTCA	84132
rs189184990	snp	C/T	0.0103295	0.0711199	intron-variant	USP42	GRCh38.p7	7:6098673	TCTCCTGCCTCAGCC[C/T]CCTGAGTAGCTGGGA	84132
rs189188663	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130901	TTCGTTGAGGTTTCC[A/G]TGGGAAAAGCAGGGT	84132
rs189194151	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6084083	CCAGGCTGGAGTGCA[C/G]TGGCTCAATCTCGGC	84132
rs189205285	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6116077	CTGCTGTACTTCAGC[C/T]TAGACAACAGAAAGA	84132
rs189219522	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6146746	ATGATGAGTTTGCTC[C/T]GCATCGCACTCTGTG	84132
rs189359951	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137486	GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG	84132
rs189362095	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6122251	GTACTTTAGTTGTAT[C/G]CCAGATATGTTGATA	84132
rs189370785	snp	C/T	0.000750831	0.0193611	missense	USP42	GRCh38.p7	7:6154108	GCGTTGGCGGAAGCC[C/T]CGGAAGGGTTGAGTC	84132
rs189438651	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6102582	CCTGGGCAACATAGC[A/G]AGCCCGTCTCTAAAA	84132
rs189449046	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131989	CCAGGCTAGAGTGCA[A/G]TGGTGTGATTATAGC	84132
rs189476720	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099507	GCGTGAGCCACTGTG[C/T]CTGGCCAATTTTTGT	84132
rs189487118	snp	C/G	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6129376	GCCTGGCCAACATGG[C/G]GAAACCCCATCTCTA	84132
rs189491432	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6153601	AACTAACCTGCACAT[C/T]GTGCACATGTAGCCT	84132
rs189523525	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134334	TTTATTTTCTCCTTG[A/T]TACCGGTCATTTCTG	84132
rs189527523	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158047	CCCTGGGGCCAACTT[C/T]GGCCAGTCACCAGAC	84132
rs189591102	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087262	TCTGGAACTCCTGAC[C/G]TCAGGTGATCTGCCC	84132
rs189601655	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103599	ACCGGTGGGGTCAGG[A/C]GGACTTGAAGGCTGC	84132
rs189609821	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124821	ATTGGCATATTTTTG[A/C]TATTTTTTTTCATGG	84132
rs189616708	snp	A/G	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6157014	AACACTTACGGATGG[A/G]AAGCAGGGATGACAG	84132
rs189617225	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6120290	CTCTGTCACTCCAGG[A/T]AGAGTGCAGTGCCAC	84132
rs189617401	snp	G/T	3.3749e-05	0.00410772	intron-variant	USP42	GRCh38.p7	7:6142899	AAGTGACGGTGTGCG[G/T]TGATGTGGTGTTTGT	84132
rs189719317	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6086611	CCCCTCAACCTCCCA[A/G]AGTTCTGGGATTACA	84132
rs189730201	snp	A/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6119876	ACCTAGCTAATTTTT[A/T]GTTTTTTTGTAGAGA	84132
rs189735953	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6150835	GAGAAATGATGATGT[A/G]AGGGTGTGCTGAGGG	84132
rs189758479	snp	C/T	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6092126	CTTCTTCCTCTTCCT[C/T]CTTCTTCTTCTTCTT	84132
rs189758674	snp	G/T	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6109079	GGGGGCCTTGAGGAG[G/T]GGTTTCTAACCCCGT	84132
rs189763464	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140257	AAAAAATGGTAATAG[A/T]AGGACAGGGTTAGTC	84132
rs189771815	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123181	GAAATGACCCTCTTC[A/T]TCCCAAATAATATTC	84132
rs189785860	snp	G/T	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6155064	CAGTGTGGAGAACAG[G/T]GACAGTCATGTTGAA	84132
rs189997619	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6079437	CACTCTAGCCTGGGC[A/G]ACAGAGCCAGACTCT	84132
rs190001847	snp	C/G	0.0182019	0.0936463	intron-variant	USP42	GRCh38.p7	7:6111715	TCAGGACATTTTCCT[C/G]CCTCAGCCTCCAGAG	84132
rs190009396	snp	A/G	0.000142876	0.0084509	intron-variant	USP42	GRCh38.p7	7:6111380	AAGGATCAAGGTACT[A/G]TTTTTCAAAAGAGAG	84132
rs190015268	snp	A/C	0.00993419	0.0697739	intron-variant	USP42	GRCh38.p7	7:6143528	TGCCTATTTTAAGAA[A/C]GCTCTTTTGTATGTT	84132
rs190210232	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6136661	GTTTGGTGAATGAAT[A/G]CTTTACTATACGCAG	84132
rs190247044	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094339	CCAGCACCTGGCTAA[A/T]TTTTTATTTTTTGTA	84132
rs190253207	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6126209	GCATAATTCTCTCAA[A/G]ATTGATCCAGGTCGT	84132
rs190267270	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107550	GAGTAGCTGGGATTA[C/T]AGGCATGCGCCACCA	84132
rs190271374	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6128523	ATTACATTTGAAGTG[A/T]GTTTTTCTGTAAACA	84132
rs190284834	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6157433	ACGGAGTCTTGCTCT[A/G]TTGCCCAGGCTGGAG	84132
rs190285232	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6160610	AATTATAAAGATAGA[C/T]AATAACTCTGTTCCA	84132
rs190419312	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117301	GTGGAATTGTACAGT[A/G]TATATTCTCATATTA	84132
rs190428980	snp	C/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6100490	GCTTGCAACCATGCC[C/T]GGCTAATTTTTGTAT	84132
rs190432988	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130311	CAGGTGGGAATTGGG[A/G]ATCGTTGTCCCTGCT	84132
rs190453054	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148132	CATTTGAGCTCAGTT[A/G]TTTGAGACCACCCTG	84132
rs190497277	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6091710	ACACACACACACACA[C/G]ACACATATATATGTT	84132
rs190504936	snp	A/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115000	CGGCCCTATATATAT[A/T]TTTTTTTAAGCAGTT	84132
rs190511282	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145765	GTTAAAATGTGAATA[C/G]CCGAGGTAAAAATAT	84132
rs190523258	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6094029	TGAGTAGCTGGTGCG[C/T]GCCACCACACCCGGC	84132
rs190567081	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151066	AGGCAGCTGTAATAC[A/G]GTGGTATTTGTGTAT	84132
rs190605190	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151960	GACCGTATGTATGAG[A/G]TACATGACTGTACTT	84132
rs190670591	snp	C/T	0.00755907	0.0610114	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104237	ACAGGCGCGCGCCAC[C/T]ACGCCCGGCTAATTT	84132
rs190679313	snp	A/T	0.0174175	0.0916809	intron-variant	USP42	GRCh38.p7	7:6095933	TTGGCTTTTTTTTTT[A/T]ATTTATTTTTTTGTA	84132
rs190681086	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133215	AGCTCAGTCAGGGTA[C/T]GAAACCATGCCTCTT	84132
rs190683511	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6120635	GTTGCCCAGGCTGGA[G/T]TGCAGTGGCACAATC	84132
rs190687279	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080658	GAGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC	84132
rs190696685	snp	A/G	0.00597247	0.0543191	intron-variant	USP42	GRCh38.p7	7:6151229	GAATGTGGAGGCCTG[A/G]GACGGTACACTACTG	84132
rs190738607	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	USP42	GRCh38.p7	7:6078587	AGCCTGGGAGACAGA[A/G]CAAGACTCCATCTCA	84132
rs190765486	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110989	ATGTTAGAAAGTACT[A/G]TTGTTTTTATATTTG	84132
rs190809403	snp	C/G	0.0142736	0.0832652	intron-variant	USP42	GRCh38.p7	7:6132600	CTGACCTCAAGTGAT[C/G]TACCCGCCTCAGCCT	84132
rs190835563	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155516	TGTTCCATCAATGAA[C/T]AATTGGGAGTCTTTG	84132
rs190839678	snp	A/G	1.68502e-05	0.00290255	synonymous-codon	USP42	GRCh38.p7	7:6140957	AGATACTTTTGATCC[A/G]TATCTTGATATAACA	84132
rs190856671	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6148630	TGGTCCTGTCGGGGC[A/G]AACAGTAGTGAGCTA	84132
rs190908392	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6084807	CACTGCAACCTCCAC[C/T]TCCCGGGTTCAAGTG	84132
rs190924459	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100338	TATTTATTTATTTTA[C/T]GGTTTTTTAATACGG	84132
rs190944153	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6116984	TTGTGCTTGCTTCCT[C/T]CCTCCCTCCCTTCCT	84132
rs191075626	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6121506	GGTAATGTTGGCATC[A/G]TGGCATGTGTTGGGA	84132
rs191083247	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104971	CCCGCCGGGCGGCTG[C/G]GCTGTGTGCGGCGGC	84132
rs191086305	snp	C/T	0.00517822	0.0506191	intron-variant	USP42	GRCh38.p7	7:6144735	ATTAGCTGGGTGTGG[C/T]GGCAGGCACTTGTAA	84132
rs191112059	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133640	CCATCCCACATCAGC[C/T]TCTGGAGTAGCTGAG	84132
rs191273045	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6160538	AACTCACTAACCCTG[C/T]GCCTCTTGTCTTTCA	84132
rs191344570	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120880	TGAGCCACTGCACCC[A/G]GCTGGAATAAATATT	84132
rs191348389	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091934	CCTTTTTCTATTCGA[C/T]ATCTGCCTGGAAAAA	84132
rs191352086	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6122484	TTTGTTTGTTTGTTT[A/G]TTTTGAGACAGAGTC	84132
rs191352746	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151751	CCCGGCCAGCAGAGT[C/T]GTTTATTGCCATTGT	84132
rs191377682	snp	A/C	0.00212973	0.0325627	missense	USP42	GRCh38.p7	7:6154640	ACCGGAGCGGGGTGG[A/C]GCTGGACTGGGTCAG	84132
rs191477530	snp	A/C	0.00438332	0.0466095	upstream-variant-2KB	USP42	GRCh38.p7	7:6077945	ACCCACCTCAGCCTC[A/C]CAAAGTGGGCGTGAG	84132
rs191487017	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6093753	ACTTCTTTTGAATGT[A/G]TTTTGTGACCAATCT	84132
rs191509411	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6110367	AAATTAAGTTAATGT[A/G]TGTCCAGCAGTTGAT	84132
rs191517615	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6142195	GTGAACATCATACTA[C/G]TAAATGAAAATTTTG	84132
rs191525832	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123908	TGAGGTGGAGTCTCA[C/G]TTTGTCACCTATGCT	84132
rs191527819	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156724	GGTTTTGTGTTTTAG[A/G]GTTTTGAATTCTGGC	84132
rs191573086	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6107965	TTTTTGGGTGATAAT[A/C]TTACCCTAGTTAAAA	84132
rs191577628	snp	C/T	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6085266	CTGGGACTACAGGTG[C/T]GCACCACCATGCCCG	84132
rs191586483	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087862	AAGACAGTGAATAAC[A/G]TACTTAACCTCTAAT	84132
rs191612170	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6138309	CAATTAGAAACAGGA[C/G]TGAAATGTTTCTGTG	84132
rs191640534	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112868	TCGAGTAGTTTGATC[A/G]CCATGTTGTTTTTGA	84132
rs191649760	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6144852	TCCAGCCTGGGCAAC[A/G]GAGTCAGATTCTGTC	84132
rs191695930	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081126	CTCCTAGGAGACTTG[A/G]TTCTGGCTGACGTGC	84132
rs191703462	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098097	TTTTAGTAGAGACGG[A/G]TTTCACCATGTTGGC	84132
rs191718684	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6113375	CTCTTTCTCCACGGC[C/T]TTCAACCTCCTGTCA	84132
rs191732094	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6127769	TGCTTTTCGTTACAA[A/G]TTATAAAATAATCTA	84132
rs191739123	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6159738	GCATCCTTCACGCAG[A/G]CAGAGTCGCCCTGTT	84132
rs191745158	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6145103	CTTTGGGAGGCCAAG[A/C]TGGGTGGATCACGAG	84132
rs191896156	snp	A/G	0.0759472	0.179459	upstream-variant-2KB	USP42	GRCh38.p7	7:6076807	TGGTCTCCATCTCCT[A/G]ACCTCATGATCCGCC	84132
rs191896188	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6109373	TTGGGCCACTCCTGA[A/G]AGGTGTTCTTTCTTC	84132
rs191900043	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6129666	AGGGATTCAAGACCA[A/G]CCTGGCCAACATGGT	84132
rs191905284	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6131865	AACTACCTCTATTCC[A/G]TCTCCCAGAAGTGCA	84132
rs191915517	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6119028	GAGACCAGCCTGGGC[A/C]ACATGTCAAGACCCT	84132
rs191929813	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127639	TGTGATGATGTATGT[A/G]TCCACCACTCTACAC	84132
rs191930676	snp	A/C	0.000761652	0.0194999	missense	USP42	GRCh38.p7	7:6149856	CCTACCAAGCCCGTT[A/C]CCTCTTCTACCATTA	84132
rs191932036	snp	C/T	0.0115144	0.0749975	intron-variant	USP42	GRCh38.p7	7:6093289	TCTTTTCTTCTCTCT[C/T]TTTTTTTTTGCCTTG	84132
rs191949250	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077165	GGCGTGATGAGCCAC[C/G/T]GTGCCGGGCCACCAG	84132
rs191966019	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6159066	GAGAAGGCCGCTGCC[C/T]GGCCCCGCCTCACCC	84132
rs192108589	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094985	TAGAGATGGAGTTTC[A/G]CCATGTTGGCCAGGC	84132
rs192113870	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6126668	TCGTGAGTGGAGCTG[C/T]GGTAAACACATCTAG	84132
rs192142485	snp	C/T	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6098547	GAATGCATTGTTTTC[C/T]TGTTTTTTGTTTTTC	84132
rs192151728	snp	G/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6128150	TAGAGATTTGGTCTC[G/T]CTGTGTTACCCAGGC	84132
rs192173699	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6098805	TCTGCCTCGGCCTCT[C/G]AGAGTGCTGGGATTA	84132
rs192175665	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6135756	ATTATTTCATTTCAG[A/G]TGTGTGCCCCTGATT	84132
rs192185446	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092777	CTGGCCAGCCACAGT[C/T]TCAGATTTCCTTCCT	84132
rs192185703	snp	C/G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6121711	GCTCTTTTGCCCAGG[C/G/T]TGGAGTACAGTGGCA	84132
rs192185955	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153242	CACACCACTGCGCTC[C/T]AGCCTGGGCAACAGA	84132
rs192188188	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6082932	TAAATTAAATATATA[C/T]AGATACATATATATA	84132
rs192195116	snp	A/C	1.66065e-05	0.00288149	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6115504	CAATTACATGCTATC[A/C]CATGAACACTCCAAA	84132
rs192203714	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6147487	AAGAAATACCTTTCA[A/G]ATGAAACAGCATCTT	84132
rs192217512	snp	C/T	0.0232847	0.105357	intron-variant	USP42	GRCh38.p7	7:6123459	ACGAGCTCAGGAGAT[C/T]GAGACCATCCTGGCT	84132
rs192389991	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117480	TTTTTCACTTTGTGC[C/T]GTTACAAATTAAGCT	84132
rs192419896	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101459	TAGGTCACAGAGCTT[A/G]TAAGAACAGAGGAAA	84132
rs192435413	snp	C/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6085902	ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCTATTA	84132
rs192437648	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118261	AAAATTAGGCCAGGT[G/T]TGGTGGTTCATGTGT	84132
rs192454277	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6131583	TCACACGAGGCTGCC[C/T]CTTCCTCATCCTTTG	84132
rs192471577	snp	C/T	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6112404	CAGTGAGCCCAAGAT[C/T]GCACCATTGCATTTC	84132
rs192480461	snp	C/G	0.0267878	0.112589	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080148	GAATGGCATGAATCC[C/G]GGAGGCAGAGCTTGC	84132
rs192504846	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6157215	GCCTCAGTGCTCATC[C/T]CTGCAGTGTGGTTCC	84132
rs192539425	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114388	ATTATAATGAACTCT[C/T]ATGTAGCCGTCAACC	84132
rs192555840	snp	C/T	0.000132912	0.00815098	intron-variant	USP42	GRCh38.p7	7:6145469	CCTGAATATGTGGAA[C/T]GATCTGTGCCCTCGG	84132
rs192657842	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106966	ATTTAGAAGCTTTAC[C/T]GAAAGTGAGGAACAT	84132
rs192688504	snp	A/G	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6136488	ATTAAAGACTATTCA[A/G]TTTAATATAACAAAT	84132
rs192696608	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6089189	AGCTGGGACTACAGG[C/T]GCCCGACACCACGCC	84132
rs192743762	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100878	TCACCATGTTGGTCA[C/T]GCTGGTCTTGAACTC	84132
rs192748891	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6130472	GTGGCAGAGTTTAGA[G/T]GTGGCTTTTTACTAC	84132
rs192804501	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123602	CGGGAGGCAGAGCCT[G/T]CAGTGAGCCGAGATC	84132
rs192814605	snp	A/G	0.0228947	0.104514	intron-variant	USP42	GRCh38.p7	7:6102219	CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	84132
rs192821006	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6156399	TGTTCAGGATGGAGC[C/T]AAAGTTGGTGAATTT	84132
rs192877214	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6089823	GGTGTGAGCTACCGC[A/G]CCCAGCCTCTTCACC	84132
rs192890374	snp	G/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6121866	AGGTCTCACTATGTT[G/T]CCCAGGGTAGTCTTG	84132
rs192903914	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153427	TGATATAACATTTTA[C/T]TTTTATTTAATAAGG	84132
rs192939232	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089681	GGGATTACAGGCATG[C/T]ACCACCACGCCTGGC	84132
rs192955553	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6145768	AAAATGTGAATACCC[A/G]AGGTAAAAATATTTC	84132
rs193018025	snp	C/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6109967	CGGCCTCCCAAAATG[C/G]TGGGATTACAGGTGT	84132
rs193019095	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141634	CGCAATATCAGCTCA[C/G]TGCATCCTCCACCTC	84132
rs193022149	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6086536	TGTATTTTTAGTAGA[C/G]ACTAGTTTTCACCAT	84132
rs193093713	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143161	CTGTCGTCCAAAGGC[A/G]AGAGCCCGGAGTGTC	84132
rs193171585	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6106390	AGAGTGCCACAGTGT[C/G]TAAATAGTGAAACTC	84132
rs193181379	snp	C/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6128618	TCTAGGCTGGGTGTC[C/G]TTCACCCTCATTTAT	84132
rs193182710	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime	USP42	GRCh38.p7	7:6160768	TGTAAAATACCGTGT[A/G]TATAAATCCCATTGA	84132
rs193245239	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6125520	CAATATTCTGCTTCT[C/T]GTGAAGTATAAGAAC	84132
rs193245949	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6149397	TTGCCAGAAAACTAG[A/G]GCCTGTGGAAAGTAT	84132
rs193298957	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6081946	TATGCAAGTTGCAGA[A/G]CAACACATAAAATAA	84132
rs199521734	snp	G/T	0.000231938	0.0107664	missense	USP42	GRCh38.p7	7:6150488	GCAACAAACTGAAAG[G/T]CTCGACGGATGAAAT	84132
rs199543868	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6085624	TATATATATATATAT[-/A]TTTTTTTTGAGATGG	84132
rs199546675	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6118553	AAGAAAAAAAAAAAA[-/C]TTTGCCTACCTACAG	84132
rs199566501	snp	A/G	5.28374e-05	0.00513964	intron-variant	USP42	GRCh38.p7	7:6145701	TGTTACATACATGCT[A/G]TAAGACAGCAGTAGC	84132
rs199569334	snp	A/G	0.00935923	0.0677645	missense	USP42	GRCh38.p7	7:6153934	GGCGCCTGGGAGGCC[A/G]TGGCCGTCGCCCCCG	84132
rs199587665	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6094823	CTTTTTTTTTTTTTT[-/G]GTCACCCAGGCTGGA	84132
rs199589142	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6141196	TGAATTTTCTTTTTC[-/T]TTTTCTTTTTTTTTT	84132
rs199657718	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6092054	TTCTTCTTCTTCTTC[C/T]TTCTTCTTCTTCTTC	84132
rs199663739	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137594	AACTCCTGACCTCAG[A/G]TGATCCACCCGTCTT	84132
rs199665296	snp	A/C	0.00516149	0.0505381	intron-variant	USP42	GRCh38.p7	7:6147715	GTCCTGTGTCACCCT[A/C]AGTATCGCTCTCCTT	84132
rs199666632	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6146671	TGTCTCAAAAAAAAA[-/A]CCAAAAACCATCAAC	84132
rs199671292	snp	G/T	0.00213433	0.0325977	synonymous-codon	USP42	GRCh38.p7	7:6149789	TCACAACAAGTTGCC[G/T]GTTCGCCAGTGTCAG	84132
rs199684634	snp	C/T	0.0230253	0.104797	synonymous-codon	USP42	GRCh38.p7	7:6154599	GCGCCGCTCTCTGGG[C/T]AGGTGCAGTCACCAC	84132
rs199890050	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6130574	TATGGTTGCAAGTCC[A/C]AGCTCCTAGTCAGCC	84132
rs199916390	in-del	-/AC/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103755	AAAAAAAAAAAAAAA[-/AC/C]CAAAACTTAAAAAAT	84132
rs199945331	snp	C/G	3.47572e-05	0.00416862	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116804	TCTCAGTCCATAATT[C/G]ATTCCCCACAGACAG	84132
rs199973271	snp	A/G/T	0.000480415	0.015492	missense	USP42	GRCh38.p7	7:6147830	ATCAGTCAGCGGGTT[A/G/T]TCACCAACAAACAGG	84132
rs200010499	snp	C/T	0.00096041	0.0218925	missense	USP42	GRCh38.p7	7:6154091	AGGGCCCGCGGGACT[C/T]GGCGTTGGCGGAAGC	84132
rs200024706	snp	A/G	0.000312867	0.0125034	synonymous-codon	USP42	GRCh38.p7	7:6155025	CGAACACGAAAATGG[A/G]AAGTCCCGGAAACGG	84132
rs200034120	snp	A/G	0.000121517	0.00779381	missense	USP42	GRCh38.p7	7:6135940	CAATGTTTGTCATCA[A/G]TGAGATGCGGCGTAA	84132
rs200050634	in-del	-/A/AA	0.463126	0.13068	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103516	CTCAAAAAAAAAAAA[-/A/AA]GAAAAAGAAAATCCC	84132
rs200071428	snp	A/C	0.000374869	0.0136855	missense	USP42	GRCh38.p7	7:6153997	GTGGGGGACACAGCA[A/C]CCCCTGACCTGTGTG	84132
rs200105504	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6092079	TTCTTCTTCTTCCTC[C/T]TCCTCTTCTTCTTCT	84132
rs200142164	snp	A/G	0.000351062	0.0132442	missense	USP42	GRCh38.p7	7:6149599	ATCCACCTCACTTAA[A/G]TGGGACTGGACCATT	84132
rs200192792	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6107409	TTTCTTCTTCCTTTT[C/T]TTTTTTTTTTTTTTT	84132
rs200231118	in-del	-/CTC	0.0119091	0.0762411	intron-variant	USP42	GRCh38.p7	7:6100179	TTCTAATGACTACTT[-/CTC]CTATATCCTCAAAAA	84132
rs200232891	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6146334	ATTCAATATTCAGTG[-/T]TTTAAAAAAAAAAAA	84132
rs200284815	in-del	-/AGGCAGAGT			intron-variant	USP42	GRCh38.p7	7:6160427	TCAGGAAGGCAGAGA[-/AGGCAGAGT]GATCTCCTCAAGGAA	84132
rs200300286	snp	A/C	0.00204837	0.0319373	missense	USP42	GRCh38.p7	7:6155010	CTCTGATCGGTTTCA[A/C]GAACACGAAAATGGA	84132
rs200357454	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6092103	TTCTTCTTCCTCCTC[C/T]TCTTCTTCTTCTTCC	84132
rs200369514	snp	C/T	1.84259e-05	0.00303523	missense	USP42	GRCh38.p7	7:6154177	CCACTCCTTGTTCAC[C/T]CCAGCGGGGACCACG	84132
rs200372288	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6142222	TCTTTTTTTTTTTTT[-/T]GAGACGGAGTCCTGC	84132
rs200398294	in-del	-/AT	0.0513262	0.151752	intron-variant	USP42	GRCh38.p7	7:6082939	AATATATATAGATAC[-/AT]ATATATATATATTTA	84132
rs200418298	snp	A/G	0.000151087	0.00869025	missense	USP42	GRCh38.p7	7:6150192	AATAGTGCAGACAGC[A/G]ACAGTGACCCGAAAG	84132
rs200429464	snp	C/T	0.000803831	0.0200317	missense	USP42	GRCh38.p7	7:6150222	GAAAACGGCCTAGCG[C/T]CTGATGGTGCCAGCT	84132
rs200454111	in-del	-/CATACA	0.00993419	0.0697739	intron-variant	USP42	GRCh38.p7	7:6091678	TAATCATTATGTTAG[-/CATACA]CACACACACACACAC	84132
rs200495011	snp	A/C/G	4.22344e-05	0.00459519	intron-variant	USP42	GRCh38.p7	7:6145670	AAGTAAGCTGTGCAG[A/C/G]TTTGCTATTAACTAT	84132
rs200506044	snp	C/T	0.000749122	0.0193391	intron-variant	USP42	GRCh38.p7	7:6149565	AGCTCTGACCAGGTG[C/T]GCTCTGCTTACTTCC	84132
rs200528323	snp	A/G	0.00174825	0.0295139	missense	USP42	GRCh38.p7	7:6154403	TCAGAAAGGTGGACC[A/G]AGGCCACTACCGCAG	84132
rs200534302	snp	A/C/T	0.000169985	0.00921758	missense	USP42	GRCh38.p7	7:6155185	GACAAACACCGAGAC[A/C/T]GCGACTCCAGGTGAG	84132
rs200556017	snp	C/T	4.2244e-05	0.00459567	missense	USP42	GRCh38.p7	7:6156777	AGGACTCAGACCTCT[C/T]AGCAGCGTGCTCTGA	84132
rs200598130	snp	A/G/T	0.000251232	0.0112055	missense	USP42	GRCh38.p7	7:6154984	CTTGTAGCCGGAGAC[A/G/T]ACTGTAACCTCTCTG	84132
rs200609357	in-del	-/TTATTTATTTAT			intron-variant	USP42	GRCh38.p7	7:6083224	GCCACCGCACCCAGC[-/TTATTTATTTAT]TTATTTATTTATTTA	84132
rs200692522	snp	C/T	0.000477365	0.015442	missense	USP42	GRCh38.p7	7:6154067	AGGACGCAAAGGGGA[C/T]GATCGCGGAGGGCCC	84132
rs200698734	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6158472	TGGAGCTGTGTGTTC[G/T]GGGGAAGGCCTGTCC	84132
rs200731155	snp	C/T	0.000447407	0.01495	synonymous-codon	USP42	GRCh38.p7	7:6150002	CAAGCTGAACTCCAG[C/T]GTGCTGGTGCCCTAT	84132
rs200753432	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6092073	TTCTTCTTCTTCTTC[C/T]TCCTCTTCCTCTTCT	84132
rs200767049	snp	A/G	0.000132492	0.00813809	missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115353	TCGCTCCTCCACAGA[A/G]AGTTCTTTTCCCATC	84132
rs200784714	in-del	-/TTCTTC			intron-variant	USP42	GRCh38.p7	7:6091979	TCAAGGACGTATTTT[-/TTCTTC]TTCTTCTTCTTCTTC	84132
rs200829371	snp	C/T	0.00299544	0.0385843	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111356	GATAAATCAAAACCA[C/T]CACCACAAAAGGATC	84132
rs200873032	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6096923	CATTTTCTTTCTTTC[-/T]TTTCTTTTCTTTTTT	84132
rs200873444	in-del	-/AAAG			intron-variant	USP42	GRCh38.p7	7:6110981	TTACAGAAATGTTAG[-/AAAG]TACTATTGTTTTTAT	84132
rs200874826	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6141566	TTGGTTATTATTATT[-/A]TTTTTTTTTTGAGAT	84132
rs200908439	snp	A/G	0.00102627	0.0226292	missense	USP42	GRCh38.p7	7:6149652	ATGTCGAGTCCTAAC[A/G]GGAATTCCAGTGTCA	84132
rs200910208	snp	C/G	4.97302e-05	0.00498624	intron-variant	USP42	GRCh38.p7	7:6150512	ATGAAATGAGGTAAC[C/G]TAAGAGTACATCTGA	84132
rs200951790	snp	C/T	0.000128789	0.00802358	synonymous-codon	USP42	GRCh38.p7	7:6154152	GCGGTCGGAGGAGCC[C/T]TGCGAGCAGCCACTC	84132
rs200959317	snp	A/G	1.72089e-05	0.00293328	missense	USP42	GRCh38.p7	7:6154273	CCTGTGCTGGACATG[A/G]CCCCGGCCGGTCACC	84132
rs200973544	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6123872	TCCAGTTTTCTTTTT[C/T]GTATCGTTTCTCTTT	84132
rs200987808	snp	A/C/G	0.00543512	0.0518475	missense	USP42	GRCh38.p7	7:6154268	CAGCTCCTGTGCTGG[A/C/G]CATGGCCCCGGCCGG	84132
rs201000582	in-del	-/C	0.493658	0.0559517	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103756	AAAAAAAAAAAAAAA[-/C]AAAACTTAAAAAATT	84132
rs201014093	snp	C/T	4.504e-05	0.00474531	intron-variant	USP42	GRCh38.p7	7:6144209	AAGGTATGTGGATGA[C/T]GTCATTAATCATGTT	84132
rs201039148	in-del	-/AGTT			downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161468	GAGATGTTTAAAGTT[-/AGTT]TGATCTTTGTTTTTC	84132
rs201039486	snp	G/T	1.84814e-05	0.00303979	synonymous-codon	USP42	GRCh38.p7	7:6154185	TGTTCACCCCAGCGG[G/T]GACCACGCCCGGGAC	84132
rs201072257	in-del	-/TG			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114647	GTGTGTATATATGTA[-/TG]TGTGTGTGTATATAT	84132
rs201085042	snp	A/G	1.65748e-05	0.00287874	utr-variant-3-prime, intron-variant	USP42	GRCh38.p7	7:6159487	AACAAAAAATTCACT[A/G]GTTATGGTAAGCTGT	84132
rs201131516	snp	A/G	0.000613645	0.0175056	intron-variant	USP42	GRCh38.p7	7:6156715	GCTGCTGGTGGTTTT[A/G]TGTTTTAGGGTTTTG	84132
rs201176874	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6129861	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	84132
rs201191443	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6087034	CTCCAGCCACCACAC[-/T]TTTTTTTTTTCTTTT	84132
rs201198108	in-del	-/T	0.0178098	0.0926698	intron-variant	USP42	GRCh38.p7	7:6152440	TTGTTGGCACTCACC[-/T]GTGGGGGTGCTGTTC	84132
rs201248764	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086238	TGAGACAGAGTCTCG[C/T]TCTGTCGCCCAGGCT	84132
rs201261995	snp	C/T	0.000139535	0.00835154	missense	USP42	GRCh38.p7	7:6150085	AGAATGGGATTGGTA[C/T]GATTGTGAGCTCCCA	84132
rs201264431	snp	A/G/T	3.36588e-05	0.00410226	intron-variant	USP42	GRCh38.p7	7:6150378	AGGCATGGAGCTGGC[A/G/T]ACTGAAGCTGAAATA	84132
rs201287707	snp	A/G	0.000120491	0.00776087	missense	USP42	GRCh38.p7	7:6156974	CCGCCTCTGGAAGGC[A/G]TCGGACCTTTCCGTG	84132
rs201311608	in-del	-/AC	0.0182019	0.0936463	intron-variant	USP42	GRCh38.p7	7:6122060	GTTTTCTGTTTCATT[-/AC]AGTTTTGTGTTTTAT	84132
rs201338882	snp	A/G	0.000461752	0.0151876	missense	USP42	GRCh38.p7	7:6155080	GACAGTCATGTTGAA[A/G]AGAAAGCCCGGAGGA	84132
rs201342208	snp	A/C/G	0.00376211	0.0432197	missense	USP42	GRCh38.p7	7:6150288	TTTGCTAAGGCAAAC[A/C/G]GTCTTCCTGGAAAGG	84132
rs201385856	in-del	-/TT			intron-variant	USP42	GRCh38.p7	7:6085622	ATATATATATATATA[-/TT]TATTTTTTTTGAGAT	84132
rs201439342	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6092066	TCTTTCTTCTTCTTC[-/T]TTCTTCTTCCTCTTC	84132
rs201451685	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6089108	GGAGTGAAGTGGTGC[A/G]ATCTCTGTTCACTGC	84132
rs201483349	in-del	-/AA	0.466927	0.124269	upstream-variant-2KB	USP42	GRCh38.p7	7:6078602	GCAAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA	84132
rs201498251	snp	C/T	0.000484283	0.0155534	synonymous-codon	USP42	GRCh38.p7	7:6154227	ATCCCAGAGCTTGGG[C/T]GCACCCGAGGCCGCA	84132
rs201567953	snp	C/G/T	0.000447502	0.014952	missense	USP42	GRCh38.p7	7:6154192	CCCAGCGGGGACCAC[C/G/T]CCCGGGACGCTCAGG	84132
rs201610818	snp	A/T	8.4735e-05	0.00650848	synonymous-codon	USP42	GRCh38.p7	7:6154980	TGCACTTGTAGCCGG[A/T]GACAACTGTAACCTC	84132
rs201617083	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6128854	CGTGGACAGGGTCTC[A/T]CTGTCACCTAGGCTG	84132
rs201634514	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120782	AGAGATGGGGTTTCA[C/T]CCTGTTGGCCAAGCT	84132
rs201656867	snp	C/T	0.000156323	0.00883953	missense	USP42	GRCh38.p7	7:6155032	GAAAATGGAAAGTCC[C/T]GGAAACGGAGACACG	84132
rs201677255	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6147988	TTGCTGTGTCCTCAA[A/G]TACATCTGAATTTCT	84132
rs201686654	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6121474	ATGCCTTTTTTTTTT[-/T]CTTGTTTTGGCATTA	84132
rs201686768	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6085618	AATATATATATATAT[A/T]TATATATTTTTTTTG	84132
rs201690340	snp	A/G	2.63932e-05	0.00363262	intron-variant	USP42	GRCh38.p7	7:6144229	TTAATCATGTTTTAT[A/G]TCGAGCCTTTCGAAG	84132
rs201699014	snp	C/G/T	0.00011441	0.00756253	intron-variant	USP42	GRCh38.p7	7:6146119	TTAATTAAATCTAAT[C/G/T]TCTCTCTTTTATTGG	84132
rs201733382	in-del	-/AA	0.0150606	0.0854603	upstream-variant-2KB	USP42	GRCh38.p7	7:6077519	AGAAAGTGAGTTTGG[-/AA]AAGATTCTTCATCCC	84132
rs201766388	snp	A/G	0.000331257	0.0128654	synonymous-codon	USP42	GRCh38.p7	7:6149885	TACCAATTCTGCAGT[A/G]CAGTCTACCTCGAAC	84132
rs201800019	snp	C/T	6.41691e-05	0.00566396	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111324	GTGCTGTAGTTTATT[C/T]GAGTTCATCTGTACC	84132
rs201836723	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6127761	AGTTACATTGCTTTT[C/T]GTTACAAATTATAAA	84132
rs201853732	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6146338	AAAAAAAAAAAAAAA[-/A]CCCAGCAGCTTAAAG	84132
rs201874634	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6133909	TTTTTTTTTTTTTTT[G/T]AGACAGCGTCTTGCT	84132
rs201893791	in-del	-/TTTATATATATA	0.152667	0.230274	intron-variant	USP42	GRCh38.p7	7:6090335	ATATATATATATTTC[-/TTTATATATATA]TTTATATATATATTT	84132
rs201917794	snp	A/C/G	0.000178419	0.00944352	missense	USP42	GRCh38.p7	7:6150066	TCAAAGGGGCTGGGC[A/C/G]AGGAGAATGGGATTG	84132
rs201918410	snp	C/G/T	0.000397469	0.014092	missense	USP42	GRCh38.p7	7:6149841	AATTCTTTGGAGAAC[C/G/T]CTACCAAGCCCGTTC	84132
rs201940898	snp	A/C			utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161891	TATCAATAGAGGCTG[A/C]TCCTTCATGCGAGCT	84132
rs201964969	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6124344	GCGATCTCGGCTCAC[C/T]GCAACCTTCACTTCC	84132
rs201973251	in-del	-/TTC			intron-variant	USP42	GRCh38.p7	7:6092096	CTCTTCTTCTTCTTC[-/TTC]CTCCTCTTCTTCTTC	84132
rs201991529	snp	C/T	0.000185512	0.00962919	synonymous-codon	USP42	GRCh38.p7	7:6154221	GGACCCATCCCAGAG[C/T]TTGGGCGCACCCGAG	84132
rs202027294	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6112471	AAAAAGAAAAAAAAA[-/G]AGAGAGCATGTAACA	84132
rs202055244	snp	G/T	0.00347224	0.0415219	synonymous-codon	USP42	GRCh38.p7	7:6154134	GAGTCCGGCTCCGCC[G/T]GCGCGGTCGGAGGAG	84132
rs202074726	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6112025	TCCTAAGTAGATGAC[G/T]TTTACAAATTTAAAG	84132
rs202078216	snp	C/T	7.80853e-05	0.00624793	missense	USP42	GRCh38.p7	7:6153959	CCCCCGAGGAGCCTC[C/T]GCCCAGCGCCGGCGA	84132
rs202090545	snp	G/T	0.000286738	0.0119703	intron-variant	USP42	GRCh38.p7	7:6150374	CAGGAGGCATGGAGC[G/T]GGCGACTGAAGCTGA	84132
rs202111561	in-del	-/TTT/TTTTTATTT			intron-variant	USP42	GRCh38.p7	7:6100006	AATTTCACAAGTCTA[-/TTT/TTTTTATTT]TTATTATTATTATTA	84132
rs202194940	snp	C/T	0.000418008	0.0144509	missense	USP42	GRCh38.p7	7:6156780	ACTCAGACCTCTCAG[C/T]AGCGTGCTCTGACGC	84132
rs367563922	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081521	GTAGCCCTTCTCCAG[A/T]CGTAAGACCCGCCCC	84132
rs367567380	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6111561	TGACAACAGGGTAGA[C/T]TGTTTTTAGTTGCTA	84132
rs367582670	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6089748	ATGTTGGTCAGGCTG[G/T]TCTCAAACTCCTGAC	84132
rs367590927	snp	C/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6127072	TTCATTTGCATTTCC[C/G]TAATGCTTAAAGGTA	84132
rs367601929	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158729	CCCATTTCAGCGAAT[C/T]GGGGAAGGAGATTCG	84132
rs367642950	snp	A/G	1.65679e-05	0.00287814	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6115477	GTGTTTAACCTACAC[A/G]CCACCTCTTGCCAAT	84132
rs367643420	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6120442	GAGATGGGGTTTCAC[A/T]GTGTTGGCCAGGCTG	84132
rs367653345	snp	A/G	4.97368e-05	0.00498657	synonymous-codon	USP42	GRCh38.p7	7:6142976	GCAGTTTGTGAAGCC[A/G]GAACAGCTTGATGGA	84132
rs367675308	snp	A/G	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6132874	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	84132
rs367710102	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6116018	GTGAGACAGGAAGGT[C/T]ACCTGAGTCTGGAAG	84132
rs367738089	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116935	CTCCCGATGTCCAGA[A/G]TTAGGTGCCTATCTT	84132
rs367745400	snp	C/T	0.00116347	0.0240911	missense	USP42	GRCh38.p7	7:6154592	CTGGCGAGCGCCGCT[C/T]TCTGGGCAGGTGCAG	84132
rs367753920	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148422	AAAGCCTGGGTGTCA[A/G]CACCTTTAAATTTTA	84132
rs367756775	snp	C/T	0.00157466	0.0280152	synonymous-codon	USP42	GRCh38.p7	7:6154539	CCAGGACCGCCACGC[C/T]CCGGAGCACCACCCC	84132
rs367760197	snp	A/C	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6160051	GTTGGATCACTTCAC[A/C]CAGCGGTCCTGGGAG	84132
rs367760345	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6086269	GGAGTGTAGTGGCGC[A/G]ATCTCAGTTCACTGC	84132
rs367767333	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6131003	CAGAGTTGCCTGGCA[C/G]CTGGCCCTGAGATGA	84132
rs367769564	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077816	CTCAGCCAACCAAGT[C/T]GCTGGGATTACAGGT	84132
rs367780926	snp	G/T	1.65605e-05	0.0028775	missense	USP42	GRCh38.p7	7:6149723	CTGGTCAGTTAATAG[G/T]TCCTCAGTGATCCCA	84132
rs367834172	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6092008	CTTCTTCTTCTTCTT[-/C]TTCTTCTTCTTCTTC	84132
rs367838211	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6147674	AAATGCTGTTGACTT[G/T]GTAAATGAATCTCTC	84132
rs367884695	snp	G/T	0.00367646	0.0427167	intron-variant	USP42	GRCh38.p7	7:6111787	TTTTTTTTTTTTTTT[G/T]TATTTTTAGTAGAGA	84132
rs367899474	snp	A/G	8.04667e-05	0.00634247	missense	USP42	GRCh38.p7	7:6155000	ACTGTAACCTCTCTG[A/G]TCGGTTTCACGAACA	84132
rs367952373	snp	C/T	1.65636e-05	0.00287776	synonymous-codon	USP42	GRCh38.p7	7:6149852	GAACCCTACCAAGCC[C/T]GTTCCCTCTTCTACC	84132
rs367966291	snp	A/T	0.000167986	0.00916323	synonymous-codon	USP42	GRCh38.p7	7:6135926	GGACGTTATTAAACC[A/T]ATGTTTGTCATCAAT	84132
rs367983845	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6124199	TTTTCTTATGATTCA[C/T]GTTAGCATGATATAT	84132
rs367997440	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6085831	TGTTGGCCAGGCTGG[C/T]TTTGAACTCCTGACC	84132
rs368118267	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6151274	ACTGCACACTTCAGC[C/T]GCACTCAATTTGTTA	84132
rs368129785	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6121891	GTCTTGAACTCCTGG[C/G]TTCAAATGATCCTCC	84132
rs368133066	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6126459	CTGGCTAATTTTTTT[G/T]GTATTTTTAGTAGAG	84132
rs368151101	snp	A/G/T			intron-variant	USP42	GRCh38.p7	7:6144592	ATTAAATAATCGGCC[A/G/T]AGTGTGGTGGCTCAC	84132
rs368159644	snp	A/G/T	3.31264e-05	0.00406968	missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115350	GCATCGCTCCTCCAC[A/G/T]GAAAGTTCTTTTCCC	84132
rs368176761	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6158142	AACAATGCGTTTCAC[A/G]TGAAAATGATGTGAA	84132
rs368181518	snp	A/G	6.62789e-05	0.00575631	missense	USP42	GRCh38.p7	7:6149628	TTGAAAGACACGCCA[A/G]GCAGTTCCATGTCGA	84132
rs368185315	snp	A/G	0.00045833	0.0151313	missense	USP42	GRCh38.p7	7:6154564	CACCCCGGCCACGGC[A/G]ACAGGCTCAGCCCTG	84132
rs368187647	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6084816	CTCCACCTCCCGGGT[G/T]CAAGTGAGTCTCCTG	84132
rs368188554	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6127030	TTACCTGTACTGATA[G/T]GTGTGTAGTGGTAAC	84132
rs368208021	snp	G/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6078174	AAAAAAAATAAGCCA[G/T]AACCATTAAGCCACC	84132
rs368222434	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6106992	AACATGCAAGTATAT[C/G]AATCTTAAGTCCTAC	84132
rs368260788	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6147103	AATGCTCATGTCTGC[A/G]CATTGAAATATTAAA	84132
rs368273741	snp	C/G	5.30903e-05	0.00515192	synonymous-codon	USP42	GRCh38.p7	7:6135890	GCAAGCACATATTAC[C/G]CAGGCACTCAGTAAT	84132
rs368286373	in-del	-/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104345	CTCGGCCTCCCAGAA[-/G]TGCTGGGATTAAGGC	84132
rs368302807	snp	C/G	9.6103e-05	0.00693125	missense	USP42	GRCh38.p7	7:6154952	ACCCCGACCGCTTCT[C/G]CCACGACAGAACTGC	84132
rs368322762	snp	C/T	6.21523e-05	0.00557425	synonymous-codon	USP42	GRCh38.p7	7:6146231	CAGCCAACAAGCCTA[C/T]GTGCTCTTTTATATC	84132
rs368327724	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6101372	TTCGGACTTGAGGGT[A/G]GGGCACTTGGAATCA	84132
rs368338461	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6093685	TTTTCTCTTCCTCTC[C/T]CTCTTTCTCTCCCCC	84132
rs368359490	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6150709	ACAGGACTGAGTCCA[C/T]GGAAACTTGATGTAC	84132
rs368396415	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6135584	TGGACCCGGGGAGGC[C/T]GAGGTTGCAGTGAGC	84132
rs368427289	snp	A/G	8.83166e-05	0.00664458	missense	USP42	GRCh38.p7	7:6157008	AAACGAAACACTTAC[A/G]GATGGAAAGCAGGGA	84132
rs368461438	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103516	GAGCAAACTCCGTCT[A/C]AAAAAAAAAAAAGAA	84132
rs368467784	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6090124	GACCAACATGGAGAA[A/C]CCCCCGCCTCTACTA	84132
rs368494814	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6127920	CCTGCTTTTTTTGTT[C/G]TTGTTGGTTTCTTTG	84132
rs368525201	snp	C/T	0.000173985	0.00932535	missense	USP42	GRCh38.p7	7:6154433	GCCGGAGAGAGCGCT[C/T]GTCCAGCGGGGAGCC	84132
rs368526993	snp	C/T	9.97805e-05	0.0070626	intron-variant	USP42	GRCh38.p7	7:6143018	CAAGTGCAGCAAGTA[C/T]GTTGGGTGGTGACTT	84132
rs368554957	snp	A/C/T	6.50277e-05	0.00570178	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111290	TCAAATCACACACTT[A/C/T]CTTTAGGACCAGTAC	84132
rs368591682	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6151265	TCTGGAAACACTGCA[C/T]ACTTCAGCCGCACTC	84132
rs368612006	in-del	-/A			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104342	CCGCCTCGGCCTCCC[-/A]GAATGCTGGGATTAA	84132
rs368640908	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080505	TGGGAGTGAGGCCAA[C/G]GTGGGTGGATCATTT	84132
rs368655873	snp	C/G/T	0.000386127	0.01389	missense, synonymous-codon	USP42	GRCh38.p7	7:6155046	CCGGAAACGGAGACA[C/G/T]GACAGTGTGGAGAAC	84132
rs368676635	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6135707	AATGAAAATGCATAA[-/G]AAGTAGATAGCTCAA	84132
rs368694025	snp	A/G	1.65726e-05	0.00287855	missense	USP42	GRCh38.p7	7:6150500	AAGGCTCGACGGATG[A/G]AATGAGGTAACGTAA	84132
rs368707906	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6144420	TCCTGCTAGACTTTG[C/T]CAGTTTTCACCAAAG	84132
rs368753126	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6146493	ACATAGTGAGACCAC[A/G]TGTCTACAAAATACG	84132
rs368769867	snp	G/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6099272	CAGGCTGGAGTGCAG[G/T]GGCGCGATCTCAGCT	84132
rs368777515	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6127666	ACACAAGTCCTTGTT[A/T]CTGTAGTTATGTAGT	84132
rs368785805	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6135705	GTAAATGAAAATGCA[A/T]AAAAGTAGATAGCTC	84132
rs368815194	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159733	GACCCGCATCCTTCA[C/T]GCAGGCAGAGTCGCC	84132
rs368828730	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6100078	GGCTGGTCTTGAACT[A/C]CTGGCCTCAAGCGAT	84132
rs368831707	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6160386	CCTGGCTGAGCTGCC[C/T]GCACCGCCAGTTCCC	84132
rs368914006	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6134599	CTGGGAGGGGCTGTC[C/T]GGTGCATTCGAGGCT	84132
rs368945539	snp	C/T	5.54739e-05	0.0052663	intron-variant	USP42	GRCh38.p7	7:6146124	TAAATCTAATCTCTC[C/T]CTTTTATTGGCTCTC	84132
rs368949041	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6117753	CCATAGGTGTGTAGT[A/G]TGGTAGTATTTTGTT	84132
rs369003430	snp	G/T	0.000149208	0.00863607	intron-variant	USP42	GRCh38.p7	7:6159405	AGAGGCCCTGGCGAT[G/T]TTGCAACCATCATTA	84132
rs369016770	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6142677	CGCTTGAGCCCAGGA[A/G]TTTGAGACCAGCCTG	84132
rs369027848	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6135678	AAAAAAAAAAAAAAA[-/G]AACAAAAAAAAGTAA	84132
rs369051655	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6079225	GAACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	84132
rs369085339	snp	A/G	3.59622e-05	0.00424026	intron-variant	USP42	GRCh38.p7	7:6147697	AATCTCTCCTAAGGA[A/G]GTGTCCTGTGTCACC	84132
rs369114720	snp	C/T	3.69884e-05	0.00430033	synonymous-codon	USP42	GRCh38.p7	7:6154182	CCTTGTTCACCCCAG[C/T]GGGGACCACGCCCGG	84132
rs369157147	snp	C/T	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6095792	TTTTTGTTTTTGAGA[C/T]AGGGTCTCACTGTTA	84132
rs369163067	snp	C/T	1.65619e-05	0.00287762	intron-variant	USP42	GRCh38.p7	7:6140110	TCTTCTCTCATGTCA[C/T]TGTTCAACGTTTTTC	84132
rs369197347	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6147537	AACGTCATTTACCCA[G/T]TTATCCTTGTTGTCT	84132
rs369290853	snp	C/G			missense	USP42	GRCh38.p7	7:6153795	TCCCGAGGACCGCGA[C/G]GCCGAGCCTCAGCCT	84132
rs369297374	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6140485	CAGCCTTCGACAGTT[-/CT]GGAGTAGTGTTCCAT	84132
rs369332625	snp	A/G	0.000159987	0.00894248	missense	USP42	GRCh38.p7	7:6150241	ATGGTGCCAGCTGCC[A/G]AGGCCAGCCTGCCCT	84132
rs369348058	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6142191	AAAAGTGAACATCAT[A/G]CTACTAAATGAAAAT	84132
rs369369720	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113812	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT	84132
rs369377115	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6158769	CTTGGTACCCGAGGA[G/T]CCGAGGATGCAGTGG	84132
rs369379436	snp	C/G	1.73788e-05	0.00294772	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116825	CCACAGACAGCTTTC[C/G]TATCACTTTTGCGCT	84132
rs369400219	snp	C/G/T			intron-variant	USP42	GRCh38.p7	7:6109403	CCTTTCCTTTTCTTT[C/G/T]TTTCTTTTCTTGAGG	84132
rs369402298	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6159858	TCCCCAGCACAGGCA[-/A]CCTCACTCAGGAGAG	84132
rs369456529	in-del	-/GA			intron-variant	USP42	GRCh38.p7	7:6159141	CCCTTGTCTTTCTCT[-/GA]TTCAAACTCCTCCTC	84132
rs369549903	snp	C/T	0.000437904	0.0147905	intron-variant	USP42	GRCh38.p7	7:6159376	ACCATAGCCACTTAA[C/T]GCACACACACAGCAG	84132
rs369591264	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6082642	TTGAGACACTGTCTC[C/T]CTCTGTCACCCAGGC	84132
rs369599830	snp	A/G			synonymous-codon	USP42	GRCh38.p7	7:6145551	TCTTGATATTCGGCC[A/G]TATATGTCTCAACCC	84132
rs369602106	snp	C/T	6.64592e-05	0.00576413	intron-variant	USP42	GRCh38.p7	7:6144081	TGTTTCTGTTTGTTT[C/T]AAGGTGTAAAAAGAT	84132
rs369604397	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6145799	TCTTGGCCGGGCGCA[A/G]TGGCTTACTCCTGTA	84132
rs369608071	snp	A/G	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6113179	GGATTACAGGTGTAG[A/G]CCACTGCACCCGGAC	84132
rs369611385	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096124	GCAGATGTTCGTGTT[C/T]TTCCACTGAGACAGC	84132
rs369615846	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6156659	TGTCTGCACAGTGAA[C/T]GTTCTCGGTGAATGG	84132
rs369623051	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104365	GGGATTAAGGCGTGA[A/G]CCACCGCGCCCGGCC	84132
rs369643801	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081095	ACCATTATTTGCTCT[C/G]ATCCTTTAGTTTAGG	84132
rs369643887	in-del	-/AT			intron-variant	USP42	GRCh38.p7	7:6090802	CATAATATATATAAC[-/AT]ATAGTTATATATATA	84132
rs369653181	snp	A/G	8.28768e-05	0.00643673	missense	USP42	GRCh38.p7	7:6147807	GCCAGTCCTCTCCCC[A/G]CCCCGTCATCAGTCA	84132
rs369702065	in-del	-/TTC			intron-variant	USP42	GRCh38.p7	7:6096930	CTTTCTTTCTTTCTT[-/TTC]TTTTTTTTTTTGAGA	84132
rs369773451	snp	C/G	6.96209e-05	0.00589963	missense	USP42	GRCh38.p7	7:6154634	CCCGACACCGGAGCG[C/G]GGTGGAGCTGGACTG	84132
rs369782517	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136808	CTTTTTTCGGTTCTT[C/T]TTTTTTTTTTTTTTC	84132
rs369785575	snp	A/G	4.96866e-05	0.00498406	missense	USP42	GRCh38.p7	7:6149748	ATCCCAGAACATCCT[A/G]AGAAACAAAAAATTA	84132
rs369788199	snp	A/C	0.000319949	0.012644	intron-variant	USP42	GRCh38.p7	7:6115574	GCGCTAACCTACTTT[A/C]ATTTTTTCCTCTGAA	84132
rs369794110	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6091856	CCTCCCAAATAGCTG[A/G]GACTACAGGGGTGCA	84132
rs369832833	snp	C/T	9.76777e-05	0.0069878	synonymous-codon	USP42	GRCh38.p7	7:6139150	TGAATTCCTTCAATA[C/T]ACTGTTGATGCTATG	84132
rs369841080	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6090469	CCTCTAATCCCGGCA[C/T]TTTGGGAGGCCAAGG	84132
rs369863349	snp	C/G	0.000464029	0.015225	intron-variant	USP42	GRCh38.p7	7:6159501	TAGTTATGGTAAGCT[C/G]TTTTCCTGTCTGTTT	84132
rs369884382	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6122556	CTCAACTGCAACCTG[C/T]GCCTCATGGGTTCAA	84132
rs369951067	snp	A/C/G	0.000208545	0.0102094	intron-variant	USP42	GRCh38.p7	7:6150313	GAAAGGTGAGTGCAC[A/C/G]TCAGGGTCTTCAGCC	84132
rs369953048	snp	A/G	8.65104e-05	0.0065763	missense	USP42	GRCh38.p7	7:6156834	AGAAGAAGAAAAAGA[A/G]GAGACATTCAAGAAA	84132
rs370027954	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6137555	TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC	84132
rs370045770	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077111	AACTCCTGATCTTGT[A/G]ATCTGCCCACCTCAG	84132
rs370074346	snp	C/G/T	0.000131832	0.00811797	missense, synonymous-codon	USP42	GRCh38.p7	7:6153966	GGAGCCTCCGCCCAG[C/G/T]GCCGGCGAGGACATC	84132
rs370093706	in-del	-/T	0.0126979	0.078662	intron-variant	USP42	GRCh38.p7	7:6124856	ACTTTAGGTTATATC[-/T]TTTAACGTATCAGTT	84132
rs370096687	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6155494	TCTTCCAGGAGTAAG[C/T]ATGCAGTGTTCCATC	84132
rs370131326	in-del	-/TTT			intron-variant	USP42	GRCh38.p7	7:6102110	GGTAGTCTCCTAAGA[-/TTT]TTTTTTTTTTTTTTT	84132
rs370177935	snp	A/G	0.000163987	0.00905353	missense	USP42	GRCh38.p7	7:6147791	CCCACCCATAGCCCC[A/G]GCCAGTCCTCTCCCC	84132
rs370179651	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6150318	GTGAGTGCACGTCAG[C/G]GTCTTCAGCCTCGTT	84132
rs370183034	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120382	CAGGTAACTGGGATT[A/G]CAGGCACGCACCATC	84132
rs370189462	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131787	TTCTACCTTTCACAG[C/T]CTTTTAAGGTTCATT	84132
rs370219757	in-del	-/T	0.0887219	0.191022	intron-variant	USP42	GRCh38.p7	7:6151604	ACCCCACCCAGCTAA[-/T]TTTTTTTTTTGTATT	84132
rs370260557	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6151135	AGGAAAACTGGCACA[C/T]CTGCACAGGGCACTT	84132
rs370274525	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6134832	GCTCTGTTGCCCAGG[C/G]TGTAGTGCAGTGGTG	84132
rs370300954	snp	C/T	7.06739e-05	0.00594407	missense	USP42	GRCh38.p7	7:6154043	CAGGCGATGCGAGCC[C/T]GTTGTCCCAGGACGC	84132
rs370313212	snp	A/G	0.000149087	0.00863257	missense	USP42	GRCh38.p7	7:6145579	CCCAACGGAGAGCCA[A/G]TTGTCTACGTCTTGT	84132
rs370358332	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6157531	GCCTCCTGAGTAGCC[A/G]GGACTACAGGCGCCC	84132
rs370415946	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126370	GCTCACTGCAGGCTT[C/T]GCCTCCTGGCTTCAC	84132
rs370422094	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6088663	ATAGCGTCTCATCAT[C/T]GATCTTTCACCATTA	84132
rs370423201	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6125259	TTTGAGAGGCTGAGG[A/C]TGGAGGATCACCTGA	84132
rs370430611	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6099494	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT	84132
rs370434357	snp	C/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161847	TGACAGCCATCCACC[C/G]TCCAATCTTACTTCA	84132
rs370494852	snp	C/T	0.000385625	0.0138803	missense	USP42	GRCh38.p7	7:6156923	ACTGTCGCCCAGTTC[C/T]GGAGAGCCCAGGGTG	84132
rs370556585	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134339	TTTCTCCTTGTTACC[A/G]GTCATTTCTGCATCT	84132
rs370581737	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137605	TCAGGTGATCCACCC[A/G]TCTTGGCCTCCCAAA	84132
rs370606288	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6159956	TGGAGCCAGCACCCC[C/G]CCAGCAGCCACCGTA	84132
rs370615204	snp	C/T	0.00024142	0.0109841	synonymous-codon	USP42	GRCh38.p7	7:6154332	CGAGAGGGTCGAGGA[C/T]GCCGCGGCGCCGAAA	84132
rs370615939	in-del	-/GTCCAGCCTGACCA			intron-variant	USP42	GRCh38.p7	7:6101879	AGGCCAGGAGTTCGA[-/GTCCAGCCTGACCA]ACATGGTGAAACCCC	84132
rs370623101	snp	A/G	3.31422e-05	0.00407063	missense	USP42	GRCh38.p7	7:6147825	CCGTCATCAGTCAGC[A/G]GGTTGTCACCAACAA	84132
rs370628315	snp	A/G	0.000437904	0.0147905	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104455	CAAGGTAGTTGCAGA[A/G]GGCGAAGCCCACGAA	84132
rs370637143	snp	C/T	0.000163733	0.00904653	synonymous-codon	USP42	GRCh38.p7	7:6154992	CGGAGACAACTGTAA[C/T]CTCTCTGATCGGTTT	84132
rs370638229	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104583	AAGCGCAGGACGAGG[C/T]GAAAGCCCAAAGTCC	84132
rs370643855	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136073	GTAGTGGCGCTATTT[C/T]GGCTCACTGCAGCTT	84132
rs370645914	snp	C/T	0.000155988	0.00883004	intron-variant	USP42	GRCh38.p7	7:6142922	GTGTTTGTGCCTCTT[C/T]TCTTCCCAGGCTGCT	84132
rs370664284	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6111625	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	84132
rs370675429	in-del	-/CCT			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081593	GACCCCGCCCCTTCT[-/CCT]TTCCGACTGGGCAGG	84132
rs370713748	snp	A/G	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6123604	GGAGGCAGAGCCTGC[A/G]GTGAGCCGAGATCGC	84132
rs370719599	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6107206	TTAAATTTTTTTTCA[C/T]TTAAGAGGCTTTTGT	84132
rs370723750	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6119932	GTCTTGAACTCCTAC[A/G]CTTAAGCGGTTCTCT	84132
rs370744249	snp	C/G/T	0.000422057	0.0145209	synonymous-codon	USP42	GRCh38.p7	7:6154167	CTGCGAGCAGCCACT[C/G/T]CTTGTTCACCCCAGC	84132
rs370752639	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB	USP42	GRCh38.p7	7:6077598	AGGAGCAGTGGCTCA[C/T]GCCTGTAGTCCCAGC	84132
rs370753120	snp	A/G	0.000166324	0.00911779	intron-variant	USP42	GRCh38.p7	7:6111403	AAAGAGAGAATTACC[A/G]CCAGAAACTCCTGTG	84132
rs370768384	snp	A/C	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6085200	TCTTCACTTACTGCA[A/C]CCTCTGCCTCCCGGG	84132
rs370775972	snp	A/G	1.65732e-05	0.00287859	intron-variant	USP42	GRCh38.p7	7:6145504	GTTTCTCCTGTTTCC[A/G]TTTCCTTCTAGGATG	84132
rs370776217	snp	A/G/T			intron-variant	USP42	GRCh38.p7	7:6084902	GTTTACATTTTTAGT[A/G/T]TAGATGGGGTTTCAC	84132
rs370777533	snp	A/G	0.000177984	0.00943188	missense	USP42	GRCh38.p7	7:6154450	TCCAGCGGGGAGCCC[A/G]CCAGAGAGAGCAGGA	84132
rs370778945	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6148070	CGGCCGAGCGCAGTG[G/T]CTCAAGCTTGTAATC	84132
rs370892498	snp	C/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6089892	TATGGCTTGCTGTGG[C/T]TGGGCGCAGGAGGCG	84132
rs370929112	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083764	GTACGTTGTTTTAGG[A/T]ACTCTCCATCTTAGG	84132
rs370964563	snp	G/T			missense	USP42	GRCh38.p7	7:6154040	TAACAGGCGATGCGA[G/T]CCCGTTGTCCCAGGA	84132
rs370978797	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125987	TGGAATATCACAAGC[A/C]CAGTAGTGACATTGA	84132
rs370996318	snp	C/T	0.000100042	0.00707183	missense	USP42	GRCh38.p7	7:6149938	GTAAAGTAACAAAAC[C/T]GATCCCCCGCAGTGA	84132
rs370998612	snp	C/G	0.000437904	0.0147905	intron-variant	USP42	GRCh38.p7	7:6122012	AATGTTACTGATCTT[C/G]TCAAAGAACGAGCTC	84132
rs371018465	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6123021	GTAGTGATGGGGTTT[C/T]GCCCGTGTTGGCTAG	84132
rs371024348	snp	C/T	0.00015341	0.00875678	synonymous-codon	USP42	GRCh38.p7	7:6149969	ATCCTGCTCCCAGCC[C/T]GTGATGAATGGCAAA	84132
rs371025803	snp	A/G	0.000569314	0.0168622	missense	USP42	GRCh38.p7	7:6154909	CCCAGCAGCCCCCGC[A/G]CAGGCGCGCCCCACG	84132
rs371071444	snp	A/G/T			intron-variant	USP42	GRCh38.p7	7:6120448	GGGTTTCACAGTGTT[A/G/T]GCCAGGCTGGTCTCA	84132
rs371094774	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126045	CACCTACAGAACCCA[A/G]CATGTTTCCCTTTCC	84132
rs371100707	snp	A/G	1.68684e-05	0.00290412	missense	USP42	GRCh38.p7	7:6140926	CAGTCAAATGTTTAA[A/G]TTGCAAGGGCGTTTC	84132
rs371110056	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6110026	TTTCGTAGAGACAGG[A/G]TCTCACCATGTTGGC	84132
rs371127204	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6157314	GTGTCACCAAAGCCC[A/T]GGAACGTACAGCTCT	84132
rs371139737	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6160056	ATCACTTCACACAGC[A/G]GTCCTGGGAGAGTCA	84132
rs371140550	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6159621	CAGAGCCATGGAGAG[A/G]CCCCGGCAGGTTCCC	84132
rs371151974	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6087921	GCTTTGTAGTCGTGT[C/T]GCAAACAGTAAATGA	84132
rs371175628	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6100353	TGGTTTTTTAATACG[G/T]AGTTTCGCTCTTGTT	84132
rs371197550	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6112900	TCCTTTAGTAAGTTT[-/C]TTTTTTTTTTTTTTT	84132
rs371197837	snp	C/G	5.7076e-05	0.00534179	intron-variant	USP42	GRCh38.p7	7:6111116	ATACATACTTTTCAT[C/G]TTTTGCAGAGTTGAA	84132
rs371199143	snp	A/C	0.000163987	0.00905353	missense	USP42	GRCh38.p7	7:6156881	AAAGATTCAGAACTG[A/C]ACTTACCCAGGGTCA	84132
rs371209184	in-del	-/TATT			intron-variant	USP42	GRCh38.p7	7:6085108	TGTTTTAGCCATTCC[-/TATT]TATTTATTTATTTAT	84132
rs371266011	snp	A/C/G	8.45316e-05	0.00650066	intron-variant	USP42	GRCh38.p7	7:6142898	CAAGTGACGGTGTGC[A/C/G]GTGATGTGGTGTTTG	84132
rs371275688	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6116059	CAGTGAGCTGTGATC[A/G]CACTGCTGTACTTCA	84132
rs371367522	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081567	GCAGTTTGGGGGCGG[A/G]GCCCGCCGCAGACCC	84132
rs371383398	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6122264	ATCCCAGATATGTTG[A/G]TATGTCATGTGTCAG	84132
rs371415361	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137904	CAGGATGGCCTCGAT[A/G]TCCTGACCTCATGAT	84132
rs371439868	snp	C/T	7.47021e-05	0.0061111	synonymous-codon	USP42	GRCh38.p7	7:6150023	GGTGCCCTATGGCGC[C/T]GAGTCCTCTGAGGAC	84132
rs371456221	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6083263	TTATTTATTTATTTA[A/T]TTATTTATTTTAGAT	84132
rs371476528	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6112959	CCCATTCTGGAATGC[A/G]GTGGCGCGATCTCGG	84132
rs371477949	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6135589	CCGGGGAGGCCGAGG[C/T]TGCAGTGAGCCAGGG	84132
rs371488627	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6121853	TTTTGTAGAGACGAG[C/G]TCTCACTATGTTGCC	84132
rs371505005	snp	A/C	0.000157988	0.00888644	missense	USP42	GRCh38.p7	7:6142994	ACAGCTTGATGGAGA[A/C]AACTCGTACAAGTGC	84132
rs371531352	snp	A/G	0.000191263	0.00977726	missense	USP42	GRCh38.p7	7:6156987	GCGTCGGACCTTTCC[A/G]TGAGAAAACGAAACA	84132
rs371557529	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132932	CATCTTGGTCTCCCA[A/G]AGTGCTGGGATTACA	84132
rs371569035	snp	C/T	0.000181984	0.00953723	missense	USP42	GRCh38.p7	7:6154570	GGCCACGGCGACAGG[C/T]TCAGCCCTGGCGAGC	84132
rs371585391	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6155303	GCCAGGCCACAGTTG[G/T]ATCCGTCTGATTTGT	84132
rs371602141	snp	A/G	3.31768e-05	0.00407275	missense	USP42	GRCh38.p7	7:6147863	GCGCCAGGCTTTATC[A/G]GACCACAGCTTCCCT	84132
rs371611764	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6121249	GGAAAAGCATTCAGT[C/T]TTTTACCATTAAGTA	84132
rs371676235	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095976	TACTGTGCTCAGGTT[A/G]GTCTCGAATTCCTAG	84132
rs371679311	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6118709	TGCATATGGATGTTC[A/G]GTTGTTCTAGCACCA	84132
rs371710604	in-del	-/AT			intron-variant	USP42	GRCh38.p7	7:6090006	ACTCTGTCTCAAAAG[-/AT]ATATATATAGGGCCA	84132
rs371714801	snp	A/G	0.001572	0.0279916	synonymous-codon	USP42	GRCh38.p7	7:6149729	AGTTAATAGGTCCTC[A/G]GTGATCCCAGAACAT	84132
rs371730573	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6079211	TACCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA	84132
rs371731198	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6122062	TTTCTGTTTCATTAC[A/T]GTTTTGTGTTTTATT	84132
rs371796866	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6102358	ATCTTGTGATCTGCC[C/T]GCCTCGGCTTCCCAA	84132
rs371811056	snp	A/G	0.00517822	0.0506191	intron-variant	USP42	GRCh38.p7	7:6108025	CCCGGCTCCACTAAA[A/G]ATACAAAAATTAGCC	84132
rs371813332	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6120646	TGGAGTGCAGTGGCA[A/C]AATCTCGGCTCACTG	84132
rs371814861	snp	A/T	0.000167986	0.00916323	intron-variant	USP42	GRCh38.p7	7:6146255	TTATATCAGGTATTG[A/T]CATGAAAACAAATTG	84132
rs371894056	snp	C/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6078728	GGTCTTGCCAACTGT[C/G]TGATGGTAAGTCCCA	84132
rs371969969	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113678	CCAGGCTGGAGAGCA[A/G]TGTTGCAATCTCGGC	84132
rs371983611	snp	C/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6126585	CCACTGTGCCGGCCT[C/G]ATAACGCCACAGTTT	84132
rs371987804	snp	A/G/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6142455	TCTCCTGACCTCATG[A/G/T]TCTGCCTGCCTTGGC	84132
rs371991911	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6158149	CGTTTCACATGAAAA[C/T]GATGTGAAATTCAGA	84132
rs372021498	snp	C/G	1.65734e-05	0.00287862	missense	USP42	GRCh38.p7	7:6150504	CTCGACGGATGAAAT[C/G]AGGTAACGTAAGAGT	84132
rs372030552	snp	A/G/T	0.00795939	0.0626292	intron-variant	USP42	GRCh38.p7	7:6121381	ATGATGCATTATTCT[A/G/T]TGTATTACTGGCTTT	84132
rs372043709	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133712	TTTAGTAGAGATGGG[A/G]TTTTTCTGTGTTGCC	84132
rs372052393	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	USP42	GRCh38.p7	7:6078496	AGTCCCAGCTACTCC[A/G]GAGGCTGAGGCAGGA	84132
rs372108268	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6111980	TGGGCAAGCATTATA[A/C]TAACTTGTTAACCAG	84132
rs372206097	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095078	TAGGTGTGAGCCACC[A/G]TGCCCAGCCCCACTT	84132
rs372212395	in-del	-/TCT			intron-variant	USP42	GRCh38.p7	7:6092083	TCTTCTTCCTCTTCC[-/TCT]TCTTCTTCTTCCTCC	84132
rs372218636	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6124324	CCAGGCTGGAGTGCA[G/T]TGGCGCGATCTCGGC	84132
rs372240911	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6130599	TCAGCCTTCTCCACC[A/G]TTAACCCAGTATGGG	84132
rs372286922	snp	C/T	2.97526e-05	0.00385687	synonymous-codon	USP42	GRCh38.p7	7:6146192	TGACTCCATTGTATC[C/T]ACCAGTGATATTAGA	84132
rs372360209	in-del	-/TC			intron-variant	USP42	GRCh38.p7	7:6092056	CTTCTTCTTCTTCTT[-/TC]TTCTTCTTCTTCTTC	84132
rs372363550	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6127089	AATGCTTAAAGGTAT[C/T]GAACATCTTTTCATG	84132
rs372364231	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6160534	CTCCAACTCACTAAC[C/G]CTGCGCCTCTTGTCT	84132
rs372385232	snp	C/T	8.28933e-05	0.00643737	intron-variant	USP42	GRCh38.p7	7:6159406	GAGGCCCTGGCGATT[C/T]TGCAACCATCATTAA	84132
rs372434961	snp	C/T	7.09379e-05	0.00595516	intron-variant	USP42	GRCh38.p7	7:6144218	GGATGATGTCATTAA[C/T]CATGTTTTATGTCGA	84132
rs372450272	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6082601	CTATTTTCTTTCTTT[C/T]TGTTTTTTTTTTTTT	84132
rs372467750	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113870	TTGTGATCCGCCCGC[C/T]TCGGCCTCCCAAAGT	84132
rs372485355	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6158882	AGGCAGCTGGTCCAG[C/T]GGGAGGGAGGTTGAA	84132
rs372540487	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6083071	ATGGAATTACAGGTG[C/T]GGGCTACCACACCTG	84132
rs372570434	snp	A/C/G			intron-variant	USP42	GRCh38.p7	7:6124620	GCTTTTTATCCAATA[A/C/G]TAGCCTCTGCCTTTT	84132
rs372626641	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117345	ACTCAGCATAATCCT[G/T]TCAACATTATTCCAT	84132
rs372637939	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6135681	AAAAAAAAAAAAGAA[-/C]AAAAAAAAGTAAATG	84132
rs372638603	snp	A/C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125912	ACATGCACTTGTAAG[A/C/G]AATAATATAGAGAAA	84132
rs372642571	snp	A/G/T	4.97668e-05	0.00498812	intron-variant	USP42	GRCh38.p7	7:6140210	GGTAAGCTTTTGCTT[A/G/T]TAAGTTGATAAAATG	84132
rs372653566	snp	A/T	5.67113e-05	0.0053247	missense	USP42	GRCh38.p7	7:6150116	CTCTCCCGGCCAAGA[A/T]GCCGAAGATGAGGAG	84132
rs372663679	in-del	-/GTA			intron-variant	USP42	GRCh38.p7	7:6111787	TTTTTTTTTTTTTTT[-/GTA]TTTTTAGTAGAGACG	84132
rs372681475	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6125449	GAGCCAAGAACACAC[A/C]ACTGCACTCCAGCCT	84132
rs372690806	snp	A/C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6137870	ATTTTTAGTAGAGAT[A/C/G]GGGTTTCACCATGTT	84132
rs372695499	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	USP42	GRCh38.p7	7:6077846	TGCCTGCCACCACAC[C/G]TAGCTAATTTTTTTG	84132
rs372720069	snp	C/T	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6156598	GGGACTACAGGTGTG[C/T]GCCACCATACCTGGC	84132
rs372750862	snp	A/G	0.0865458	0.189163	intron-variant	USP42	GRCh38.p7	7:6135678	AAAAAAAAAAAAAAA[A/G]AACAAAAAAAAGTAA	84132
rs372764421	snp	G/T	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6096568	GTCTGTCAGGAGCTG[G/T]TTTAAACTAACAAGG	84132
rs372790896	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080564	CAACATAGTGAAACC[A/G]CGTCTCTACTAAAAA	84132
rs372821842	snp	C/G	0.000215308	0.0103734	missense	USP42	GRCh38.p7	7:6149845	CTTTGGAGAACCCTA[C/G]CAAGCCCGTTCCCTC	84132
rs372870178	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6112813	CAATTTGTCTTCCAG[C/T]GTGGCCCAGGGAAGC	84132
rs372922724	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142320	CTCCTGGGTTCAGGC[A/G]ATTCTTCTGCCTCAA	84132
rs372942471	snp	A/G	3.31461e-05	0.00407086	synonymous-codon	USP42	GRCh38.p7	7:6149909	CTCGAACGCATCTAC[A/G]ATGTCAGTTTCTAGT	84132
rs373007004	snp	C/T	0.0418186	0.138422	intron-variant	USP42	GRCh38.p7	7:6091718	ACACACACACACATA[C/T]ATATGTTGCTGATTT	84132
rs373020846	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137881	AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	84132
rs373034123	snp	G/T	0.0178098	0.0926698	intron-variant	USP42	GRCh38.p7	7:6152442	GTTGGCACTCACCTG[G/T]GGGGGTGCTGTTCAT	84132
rs373068279	snp	C/T	4.33191e-05	0.00465378	intron-variant	USP42	GRCh38.p7	7:6139227	CCAGCCATGTCTTCA[C/T]TGGGGATCTCTGGTT	84132
rs373079438	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6119501	GTTGTTCTGGCTCTT[C/G]ATGGTTGCTTGGCCA	84132
rs373138875	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086765	GAGTTTCGCTCTTGT[C/T]GCCCAGGCTGGAATG	84132
rs373178582	in-del	-/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6078620	AAAAAAAAAAAAAAA[-/T]AGCTTAAGCCAAGGC	84132
rs373181771	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088382	TGCCTCAGCCTCCCA[A/T]GTAGCTGGGATTAAA	84132
rs373214969	snp	C/T	2.01782e-05	0.00317627	synonymous-codon	USP42	GRCh38.p7	7:6156790	CTCAGCAGCGTGCTC[C/T]GACGCTGACCTCCAC	84132
rs373305632	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6087693	TTTTTCAGCGAGAGT[A/G]TGAATCTTCTCCAAC	84132
rs373308984	snp	A/G	1.73788e-05	0.00294772	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116836	TTTCCTATCACTTTT[A/G]CGCTTAATGAAAGTA	84132
rs373310797	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6132774	CCTCCCGGGTTCACG[C/G]CATTCTCCTGCCTCA	84132
rs373312413	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6096748	ATACTGTGCTTTTGT[A/T]GACAGCCTGTCTTGC	84132
rs373360781	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6156000	AGACTCAAGCGATCC[C/G]AAAGCACTGGGATCA	84132
rs373376184	snp	C/T	0.000171985	0.00927162	synonymous-codon	USP42	GRCh38.p7	7:6140966	TGATCCATATCTTGA[C/T]ATAACATTGGAGATA	84132
rs373390788	snp	A/G	1.65946e-05	0.00288046	missense	USP42	GRCh38.p7	7:6147792	CCACCCATAGCCCCG[A/G]CCAGTCCTCTCCCCG	84132
rs373397877	snp	A/G	0.000159987	0.00894249	missense	USP42	GRCh38.p7	7:6154675	CACTACACCGAGGGC[A/G]AGCGTGGCTGGGGCC	84132
rs373459793	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077158	GATTACAGGCGTGAT[A/G]AGCCACCGTGCCGGG	84132
rs373488454	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6136876	CTTGAACTCCTGGCT[C/T]AAGTGATCCTCTTGC	84132
rs373489451	snp	C/G	3.69857e-05	0.00430017	intron-variant	USP42	GRCh38.p7	7:6150345	CGTTTGTGGCGGTTC[C/G]CTTGGCTGGATTTCA	84132
rs373490173	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114412	GTCAACCAACTTTGA[C/T]ATTTATCAACTTACG	84132
rs373494515	snp	A/G	5.09697e-05	0.00504799	missense	USP42	GRCh38.p7	7:6156845	AAGAAGAGACATTCA[A/G]GAAAATCAGAGGACT	84132
rs373507172	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104091	CTTTTCTTTTCTTTT[C/T]TGAGACAGACTCTCG	84132
rs373581855	snp	C/T	0.000100475	0.00708712	intron-variant	USP42	GRCh38.p7	7:6145697	CTATTGTTACATACA[C/T]GCTATAAGACAGCAG	84132
rs373600173	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6133805	GATGACAGGCGTAAG[C/G]CACCGCACCTGGTGC	84132
rs373604556	snp	A/G			missense	USP42	GRCh38.p7	7:6154679	ACACCGAGGGCGAGC[A/G]TGGCTGGGGCCGGGA	84132
rs373665800	snp	A/C	0.000392388	0.0140014	missense	USP42	GRCh38.p7	7:6155012	CTGATCGGTTTCACG[A/C]ACACGAAAATGGAAA	84132
rs373682976	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6136021	TTTTTTTTTTTTTTT[-/C]CGAGACAGAGTCTTG	84132
rs373689781	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6141201	TTTTCTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT	84132
rs373694269	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6146690	AAAACCATCAACTCT[A/G]CCATGTGCCTGGAGA	84132
rs373698987	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6135594	GAGGCCGAGGTTGCA[A/G]TGAGCCAGGGTCACA	84132
rs373704577	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152929	GGAAAGGAGGAGGCC[C/T]TGTCATCACTGGACT	84132
rs373791380	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6119265	CTTTGTTCTTTCTCC[A/G]AGTTATGCTGTAGCC	84132
rs373801453	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099561	GTATGTTGGGCAGGC[A/G]GGTCTCAAACTCCTG	84132
rs373816337	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6132209	GAGATTACAGGGCAG[C/T]CACCACACCTGGCCC	84132
rs373827893	snp	A/C	0.000437904	0.0147905	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104491	GGATTTCTCGGAGCC[A/C]AGTCCGTTTTCGGGG	84132
rs373857672	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6098702	GATGTGCACCACCAC[A/C]CCTGGCTAATTTTTG	84132
rs373861053	snp	C/T	2.95819e-05	0.00384578	missense	USP42	GRCh38.p7	7:6154246	CCCGAGGCCGCAGAG[C/T]GGCCGCCAGCTCCTG	84132
rs373865985	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120093	CCTCAGCTTCCTGAG[C/T]GGTTGGGACTACAGG	84132
rs373906321	in-del	-/TGTATA			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114655	ATATGTATGTGTGTG[-/TGTATA]TATATATATATATAT	84132
rs373978759	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152635	GGACACTCGCTCCCT[C/T]GGCCAGGGGACTCTG	84132
rs373979297	snp	C/T	0.00017685	0.0094018	synonymous-codon	USP42	GRCh38.p7	7:6154281	GGACATGGCCCCGGC[C/T]GGTCACCCGGAAGGG	84132
rs373988849	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6092369	TTTTTAGTAGAGATG[C/G]GGTTTCACCATGTTG	84132
rs373991514	snp	A/G	0.000132564	0.00814031	missense	USP42	GRCh38.p7	7:6147819	CCCGCCCCGTCATCA[A/G]TCAGCGGGTTGTCAC	84132
rs373995572	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104453	CGCAAGGTAGTTGCA[A/G]AGGGCGAAGCCCACG	84132
rs374021905	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6144551	GCATGCAAGAGAAAT[A/G]AACGATCCATTCCTG	84132
rs374046009	snp	A/G/T	0.000119657	0.00773413	missense	USP42	GRCh38.p7	7:6149970	TCCTGCTCCCAGCCC[A/G/T]TGATGAATGGCAAAT	84132
rs374091755	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6097581	CCAGCCATGTGGGTT[A/C]TTTCTTTTTCTTTTC	84132
rs374091994	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6079390	TTGAACCCCGGAGGC[A/G]GAGCTTGCAGTGAGC	84132
rs374138161	snp	C/T	1.68142e-05	0.00289945	intron-variant	USP42	GRCh38.p7	7:6142905	CGGTGTGCGGTGATG[C/T]GGTGTTTGTGCCTCT	84132
rs374139821	in-del	-/A/AA			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080222	GCGAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA	84132
rs374151941	snp	A/G	1.66679e-05	0.00288681	missense	USP42	GRCh38.p7	7:6156891	AACTGCACTTACCCA[A/G]GGTCACCAGCTTGGA	84132
rs374160888	snp	A/G	0.00241154	0.0346403	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115285	TAGCTTCAGTATGCA[A/G]AGCTTGGTTTCTGAC	84132
rs374191297	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6121314	AGGTTGAGTTGTTTG[A/G]TGCTTGAATGTTAAA	84132
rs374236213	snp	C/G/T			intron-variant	USP42	GRCh38.p7	7:6088338	TCGGCTCACTGCAAC[C/G/T]TCTGCCTCCCAGGTT	84132
rs374262203	snp	A/C/G/T	6.62489e-05	0.00575509	synonymous-codon	USP42	GRCh38.p7	7:6149765	GAAACAAAAAATTAC[A/C/G/T]ATCAGTATTCACAAC	84132
rs374262234	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6123087	TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTATA	84132
rs374270947	snp	C/G/T	0.000168819	0.00918592	missense	USP42	GRCh38.p7	7:6154492	GGCCACCGTCACCGG[C/G/T]GGCGCCGCACCTGCC	84132
rs374313153	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6146093	ATATTTCTCTTGACT[A/G]TGTTCCATGTTTAAT	84132
rs374359350	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6145079	TGGCTCATGCCTATA[A/G]TTCTAGCACTTTGGG	84132
rs374366035	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6139491	CTGCAGATCTCAAAC[C/T]AGCTGCTTCTCCTTT	84132
rs374369760	snp	A/G	8.33702e-05	0.00645586	synonymous-codon	USP42	GRCh38.p7	7:6149939	TAAAGTAACAAAACC[A/G]ATCCCCCGCAGTGAA	84132
rs374371362	snp	A/C	0.000791989	0.0198839	missense	USP42	GRCh38.p7	7:6154931	CGCCCCACGCCCTCG[A/C]CCCGCACCCCGACCG	84132
rs374371556	snp	A/C			missense	USP42	GRCh38.p7	7:6154249	GAGGCCGCAGAGCGG[A/C]CGCCAGCTCCTGTGC	84132
rs374377877	snp	A/C/T	0.000160858	0.00896688	synonymous-codon	USP42	GRCh38.p7	7:6154107	GGCGTTGGCGGAAGC[A/C/T]CCGGAAGGGTTGAGT	84132
rs374395528	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6099211	CCCATTGTTCCCTCT[C/T]TTTTTTTTTTTTTTT	84132
rs374415802	snp	A/C	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6089677	AGCTGGGATTACAGG[A/C]ATGCACCACCACGCC	84132
rs374422412	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6107749	TTTTCTTCTGTCCCC[A/G]CACTGTTTCATAATT	84132
rs374438551	snp	A/T	0.00250622	0.0353105	intron-variant	USP42	GRCh38.p7	7:6150383	TGGAGCTGGCGACTG[A/T]AGCTGAAATATTTTT	84132
rs374482299	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6120455	ACAGTGTTGGCCAGG[A/C]TGGTCTCAAACTCCT	84132
rs374544689	snp	A/G	0.0115144	0.0749975	intron-variant	USP42	GRCh38.p7	7:6106805	TCCTGGGCTCAAGCC[A/G]TCCTGCTGCCTTGGC	84132
rs374545879	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123495	GGTGAAACCCCGTCT[C/G]TACTAAAAATACAAA	84132
rs374549338	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6098056	ATTACAGGCACACAC[C/T]ACTACCCCACAGCTA	84132
rs374573042	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6084221	TAGTAGAGACAGGGT[A/T]TCACCATGTTGACCA	84132
rs374635482	snp	C/T	3.32259e-05	0.00407576	missense	USP42	GRCh38.p7	7:6147875	ATCGGACCACAGCTT[C/T]CCTCTCACATGATAA	84132
rs374686078	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096268	ACTTGAGGCCAGCAG[C/T]TCGAGACCAGCTTAT	84132
rs374697905	snp	G/T	0.000247262	0.0111162	missense	USP42	GRCh38.p7	7:6154053	GAGCCCGTTGTCCCA[G/T]GACGCAAAGGGGATG	84132
rs374789343	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6094562	TTAAGCTGGTGCTAG[A/T]TGAGTCCTTGAGGAT	84132
rs374814529	snp	A/G	3.6901e-05	0.00429525	missense	USP42	GRCh38.p7	7:6135915	AGTAATCCTGGGGAC[A/G]TTATTAAACCAATGT	84132
rs374831681	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086187	ATTACAGGAGCCTGC[C/T]ACCTCACCTGGCTAA	84132
rs374837710	snp	C/T	0.000244051	0.0110438	synonymous-codon	USP42	GRCh38.p7	7:6154995	AGACAACTGTAACCT[C/T]TCTGATCGGTTTCAC	84132
rs374860995	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6131126	GCACGAACGCTGAGC[A/C]CTTTGCTACCTCTAA	84132
rs374932330	snp	C/G/T			intron-variant	USP42	GRCh38.p7	7:6151916	TATGTTGTGATCTTA[C/G/T]GGACCGCCATCATAT	84132
rs374935996	snp	A/G	0.000195557	0.00988637	intron-variant	USP42	GRCh38.p7	7:6147722	GTCACCCTAAGTATC[A/G]CTCTCCTTGTTTCCA	84132
rs374947317	snp	C/T	3.31389e-05	0.00407042	missense	USP42	GRCh38.p7	7:6150491	ACAAACTGAAAGGCT[C/T]GACGGATGAAATGAG	84132
rs374956320	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6109861	ACGTGCCACCACGCC[C/T]GGCTAATTTTTGTAT	84132
rs374960858	snp	A/G	6.63119e-05	0.00575774	synonymous-codon	USP42	GRCh38.p7	7:6142961	CAACAAGGCATTGGA[A/G]CAGTTTGTGAAGCCG	84132
rs374964350	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121859	AGAGACGAGGTCTCA[C/G]TATGTTGCCCAGGGT	84132
rs374967794	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135788	GTAATTAGCCTTGAT[G/T]TGTGTATATGGTTGT	84132
rs374969700	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6101425	ATTTCAATAAAGGAA[A/T]CAGGTTAAGTAATTT	84132
rs374991376	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6151431	CTGTACAAAAATAAC[C/T]TCTTTTTTTGTTTGT	84132
rs375014786	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6156643	AGATAAGAATTGTGC[A/G]TGTCTGCACAGTGAA	84132
rs375026446	snp	G/T	3.31203e-05	0.00406928	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115384	TGAGAAGATTTGTCT[G/T]AAGTGGCAACAAACT	84132
rs375042824	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6102522	ATCCCAGCACTTTGG[C/G]AGGTCCAAGCAGAGG	84132
rs375045630	snp	G/T	0.00398564	0.0444627	downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161733	ATTGGAGGGGTGTTT[G/T]CTGGACCCAACAATA	84132
rs375114842	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6136549	TAATTGGTAAGTTTT[A/G]TAGTGTCTTTGCTCT	84132
rs375124524	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6085999	CTGGCTGCCAACATC[A/G]AGATGAGAGAAACCA	84132
rs375135245	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114478	CATTATCTCAAATCC[A/G]ATACTTCATCTTTCA	84132
rs375135344	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6130060	GTGTAATCATGGCTC[A/C]CTGCAGCTCCCACCT	84132
rs375186620	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6148079	CAGTGGCTCAAGCTT[-/T]GTAATCCCAGCACTT	84132
rs375226837	snp	A/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113751	CTCAGCCTCCTGAGT[A/T]GCTGGGACTACAGGT	84132
rs375267101	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6079148	AACTGAAAATATCAG[C/G]AGCCATATTTTAAAA	84132
rs375285669	snp	A/G	2.89742e-05	0.00380608	missense	USP42	GRCh38.p7	7:6146202	GTATCTACCAGTGAT[A/G]TTAGATCGGTACTCA	84132
rs375294510	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6111629	TTTTTTTGAGACGGA[C/G]TCTCGCTCTGTCACC	84132
rs375308599	snp	C/G/T	0.000283188	0.0118961	missense, synonymous-codon	USP42	GRCh38.p7	7:6154023	GTGTGATCCCGGGAG[C/G/T]TTAACAGGCGATGCG	84132
rs375344760	snp	C/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115192	AAATGTCCCTCTTCC[C/G]CCTGTATTTCAGGTA	84132
rs375401959	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136168	TACCACTATGCCAGG[C/T]TAATTTTGTACTTTT	84132
rs375411636	snp	A/G			intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153166	TAATCCCAGCTACCC[A/G]GGAAGCTGGGTCAGG	84132
rs375446417	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6090381	ATATTTCTTTATATA[C/T]ATTATATAGGTTTAT	84132
rs375556341	snp	A/C/T	1.7731e-05	0.00297744	missense	USP42	GRCh38.p7	7:6154081	ATGATCGCGGAGGGC[A/C/T]CGCGGGACTCGGCGT	84132
rs375578428	snp	A/G	3.65337e-05	0.00427382	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111134	TTGCAGAGTTGAACA[A/G]TGACCATAGTTGACA	84132
rs375580930	snp	A/G	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6146976	CCAGCACCCGCACCC[A/G]GCTCTGTCCTGTTGT	84132
rs375587591	snp	C/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6124978	TTGTGGTCAGGAATT[C/T]GAGACCAGCCTGGCC	84132
rs375593932	snp	A/G	8.77078e-05	0.00662165	missense	USP42	GRCh38.p7	7:6154405	AGAAAGGTGGACCGA[A/G]GCCACTACCGCAGCC	84132
rs375619055	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6132098	CCACCATGCCTGGCT[A/T]ATTTTTTGTAGAGAC	84132
rs375624699	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6109250	CAGGGACAAAAGAAA[A/G]AAAAACAAGACTTCA	84132
rs375627119	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6087603	CGGCCTCCCAAAGTG[A/C]TGGGATTACAGGAAT	84132
rs375648875	snp	C/T	6.95253e-05	0.00589558	intron-variant	USP42	GRCh38.p7	7:6150312	GGAAAGGTGAGTGCA[C/T]GTCAGGGTCTTCAGC	84132
rs375651984	snp	A/C	1.91334e-05	0.00309295	missense	USP42	GRCh38.p7	7:6156812	GACCTCCACAGACAC[A/C]AAAAAAAGAAGAAGA	84132
rs375687361	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136021	TTTTTTTTTTTTTTT[C/T]CGAGACAGAGTCTTG	84132
rs375713023	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6110299	TTGCTGACTGGTTGC[C/T]TCATTTTATAGGCCC	84132
rs375736931	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6112550	AACTCATCCAGATAA[A/G]TGAGACAGTAACACT	84132
rs375743154	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6097086	TAATTTTGTATGTTT[A/G]GTAGAGACGGGCTGC	84132
rs375745596	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6079224	AGAACTTTGGGAGGC[C/G]AAGGCGGGCGGATCA	84132
rs375750717	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6108220	CAAACAAAAAAATTA[C/T]AAGTAACAAAATTGA	84132
rs375752290	snp	C/T	0.000183983	0.00958946	missense	USP42	GRCh38.p7	7:6154274	CTGTGCTGGACATGG[C/T]CCCGGCCGGTCACCC	84132
rs375755874	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	USP42	GRCh38.p7	7:6077085	TCACCATATTGGTCC[A/G]GCTGGTCTTGAACTC	84132
rs375772971	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6129728	TAGCCAGGTGTGGTG[G/T]TGCACACCTCTAATC	84132
rs375841882	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106859	GCTTGGTCCACCATG[C/T]CCCACCTGTAGGTTG	84132
rs375844237	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6093157	TCCCTCTCTCCCTCC[C/T]TCCCTTCCCTTCCTT	84132
rs375859355	in-del	-/T/TT/TTT			intron-variant	USP42	GRCh38.p7	7:6111769	ACCAAGCCCGGCTAA[-/T/TT/TTT]TTTTTTTTTTTTTTT	84132
rs375867432	snp	C/T	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6113371	GGACCTCTTTCTCCA[C/T]GGCCTTCAACCTCCT	84132
rs375914959	in-del	-/TTTG			intron-variant	USP42	GRCh38.p7	7:6122465	GTTTTGTTTTGTTTT[-/TTTG]TTTGTTTGTTTGTTT	84132
rs375921996	snp	A/G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6122267	CCAGATATGTTGATA[A/G/T]GTCATGTGTCAGTTT	84132
rs375929061	snp	C/T			utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081728	TCGCGCTGCTGAAAG[C/T]CGACTGCGCCTACGT	84132
rs375945715	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095062	CAAAGTGCTGGCATT[A/T]TAGGTGTGAGCCACC	84132
rs375947233	snp	C/T	3.31208e-05	0.00406931	missense	USP42	GRCh38.p7	7:6149679	GTCAACAGGGCTAGT[C/T]CTGTTAATGCTTCAG	84132
rs375949266	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152544	CCTCTGTTAGGAGGG[C/T]GTAGATATTAAACCG	84132
rs375977254	snp	A/C	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6087290	CCCGCCTTGGCCTAC[A/C]AAAGTGCTGGGATTA	84132
rs376007876	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6141099	ATTGAAAAATTCAAT[A/G]TGCTAAGATTTCATT	84132
rs376047424	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6156485	GACAGGGTCTTGCTC[A/T]GTTGCCCAGGCTGGA	84132
rs376081299	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6160366	GGCCCAGCAGATGGC[A/G]CCTCCCTGGCTGAGC	84132
rs376125328	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6158581	GTTGCGGGGTGAGCC[C/T]CATGGGGGACATTTG	84132
rs376183536	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6128256	TGTGCCTGGCCCTGC[-/T]TTTTTTTTTTTTTTT	84132
rs376195442	snp	A/T	1.65707e-05	0.00287838	missense	USP42	GRCh38.p7	7:6150498	GAAAGGCTCGACGGA[A/T]GAAATGAGGTAACGT	84132
rs376216271	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6137892	CACCATGTTAGCCAG[C/G]ATGGCCTCGATATCC	84132
rs376220078	snp	A/G/T	9.95515e-05	0.00705461	synonymous-codon	USP42	GRCh38.p7	7:6143000	TGATGGAGAAAACTC[A/G/T]TACAAGTGCAGCAAG	84132
rs376248062	in-del	-/GGT			intron-variant	USP42	GRCh38.p7	7:6098910	AGTCTTCGGGTTGGT[-/GGT]ACCATTCTTGAACAA	84132
rs376251087	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6122716	GCCTTGTGATCCACC[C/T]GCCTCAGCCTCCCAA	84132
rs376260428	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6157461	GAGTGCAGTGGCGGC[A/G]ATCTCAGCTCACTGC	84132
rs376282709	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6105706	CCCAAAAGCATGTGT[G/T]CCTCTCTAGCGTTTT	84132
rs376347056	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6112942	AGAGTCTCGCTCTGT[C/T]GCCCATTCTGGAATG	84132
rs376372245	snp	A/G	1.68468e-05	0.00290226	synonymous-codon	USP42	GRCh38.p7	7:6156853	ACATTCAAGAAAATC[A/G]GAGGACTTTGTTAAA	84132
rs376378452	snp	C/T	3.67471e-05	0.00428628	intron-variant	USP42	GRCh38.p7	7:6150351	TGGCGGTTCCCTTGG[C/T]TGGATTTCAGGAGGC	84132
rs376395523	snp	A/G	1.75019e-05	0.00295815	synonymous-codon	USP42	GRCh38.p7	7:6156997	TTTCCGTGAGAAAAC[A/G]AAACACTTACGGATG	84132
rs376412352	snp	C/T	0.00017917	0.00946323	synonymous-codon	USP42	GRCh38.p7	7:6154707	GGAGAAGTTCTACCC[C/T]GACAGGCCGCGCTGG	84132
rs376429774	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6143470	TTGCTGAAAAACTCT[A/G]ATTTTGATCATTCAT	84132
rs376435812	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6109985	GGATTACAGGTGTGC[A/T]CCACCATGCCTGGGT	84132
rs376440635	snp	A/C/T	6.63713e-05	0.00576032	intron-variant	USP42	GRCh38.p7	7:6150532	AGTACATCTGAGGCA[A/C/T]GTGTGGCAGCATAGT	84132
rs376450151	snp	C/G	0.00131314	0.0255899	intron-variant	USP42	GRCh38.p7	7:6122009	TTTAATGTTACTGAT[C/G]TTCTCAAAGAACGAG	84132
rs376451090	snp	A/G	1.65971e-05	0.00288067	missense	USP42	GRCh38.p7	7:6149926	TGTCAGTTTCTAGTA[A/G]AGTAACAAAACCGAT	84132
rs376482503	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6122063	TTCTGTTTCATTACA[G/T]TTTTGTGTTTTATTG	84132
rs376482831	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6082866	TCTACCTGCCTTGGC[C/G]TCCCAAAGTGCTGGG	84132
rs376502671	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6083262	TTTATTTATTTATTT[A/T]TTTATTTATTTTAGA	84132
rs376510026	in-del	-/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081536	ACGTAAGACCCGCCC[-/C]ACCCACGCGCGCGCC	84132
rs376554110	snp	G/T	0.000167986	0.00916322	synonymous-codon	USP42	GRCh38.p7	7:6135950	CATCAATGAGATGCG[G/T]CGTAAGTATTAACTA	84132
rs376560447	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6087135	CTCCCATGTTCAAGC[A/G]ATTCTCCTGCCTCAG	84132
rs376563674	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6149297	CATGCCACAGGTCCT[A/G]CTGATTTCGATCAGA	84132
rs376617636	snp	C/G	3.31318e-05	0.00406999	missense	USP42	GRCh38.p7	7:6150473	AGACCTTCAGGCTTA[C/G]CAACAAACTGAAAGG	84132
rs376619670	in-del	-/TCT			intron-variant	USP42	GRCh38.p7	7:6092082	TCTTCTTCCTCTTCC[-/TCT]TCTTCTTCTTCTTCC	84132
rs376639934	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130197	TGAGTCTTATCTAAC[C/T]TTTGTTTTAGCCAAC	84132
rs376662963	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079902	ATACATTTTTCTGAC[C/T]ACATTTCACCCCCCT	84132
rs376710304	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096855	TGTACCAATCATGCC[C/T]ACCTTCTGCTGCGTA	84132
rs376728655	snp	C/G	7.75916e-05	0.00622814	missense	USP42	GRCh38.p7	7:6154628	ACCACTCCCGACACC[C/G]GAGCGGGGTGGAGCT	84132
rs376780738	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6110369	ATTAAGTTAATGTAT[A/G]TCCAGCAGTTGATGC	84132
rs376787076	in-del	-/ACAC/ACACACAC			intron-variant	USP42	GRCh38.p7	7:6091680	TCATTATGTTAGCAT[-/ACAC/ACACACAC]ACACACACACACACA	84132
rs376792206	snp	A/G	0.000343702	0.0131047	intron-variant	USP42	GRCh38.p7	7:6144232	ATCATGTTTTATGTC[A/G]AGCCTTTCGAAGCTT	84132
rs376858924	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6142674	GATCGCTTGAGCCCA[A/G]GAGTTTGAGACCAGC	84132
rs376865105	snp	G/T	0.00953873	0.0683987	intron-variant	USP42	GRCh38.p7	7:6109659	TTGGCCTCCCAAAGT[G/T]CTGGGATTACAGGGG	84132
rs376872215	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6136808	TTTTTTCGGTTCTTC[-/T]TTTTTTTTTTTTTTC	84132
rs376875644	snp	C/T	0.000285959	0.011954	intron-variant	USP42	GRCh38.p7	7:6142881	AGGGCAAGACCCAAA[C/T]ACAAGTGACGGTGTG	84132
rs376926258	snp	C/T	0.000335093	0.0129396	missense	USP42	GRCh38.p7	7:6154349	CCGCGGCGCCGAAAG[C/T]CCCAGGCCCTTCCCC	84132
rs376930802	snp	G/T	0.000165986	0.00910855	intron-variant	USP42	GRCh38.p7	7:6111111	AACAAATACATACTT[G/T]TCATCTTTTGCAGAG	84132
rs376948986	in-del	-/TGAAGC			intron-variant	USP42	GRCh38.p7	7:6158373	GTTCACGTGTGAAGC[-/TGAAGC]GCATCCCCTCCTCCC	84132
rs376970933	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6158192	TGGCTTGATTGGGGC[A/G]CAGCCAGGTGCGTTC	84132
rs376976590	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6118573	CCTACCTACAGGTCA[C/G]AAATATTTTTCCTAT	84132
rs377012531	snp	C/T	0.000215855	0.0103866	intron-variant	USP42	GRCh38.p7	7:6145482	AATGATCTGTGCCCT[C/T]GGAAATGTTTCTCCT	84132
rs377023378	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6082581	AACATAAGGAGACTG[C/T]GTCTCTATTTTCTTT	84132
rs377063477	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6083508	TAATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	84132
rs377080277	snp	C/T	1.73797e-05	0.0029478	intron-variant	USP42	GRCh38.p7	7:6116758	TTGTTATGCCAGAAT[C/T]AACGTTCTGTTTGCC	84132
rs377134337	snp	A/G	0.000235193	0.0108416	missense	USP42	GRCh38.p7	7:6155090	TTGAAAAGAAAGCCC[A/G]GAGGAGCGAACAGAA	84132
rs377136354	snp	C/T	8.45273e-05	0.0065005	synonymous-codon	USP42	GRCh38.p7	7:6139108	TATAGCTAGGCACTT[C/T]CGTTTTGGAAACCAA	84132
rs377160611	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104296	ACCATGCTGGCCAGG[C/G]TAGTCTCGAACTCCT	84132
rs377225532	snp	A/T	0.00993419	0.0697739	intron-variant	USP42	GRCh38.p7	7:6124647	TTTTATTTTGAGGCA[A/T]TATACCTTTTACATT	84132
rs377237604	snp	A/G	6.6986e-05	0.00578692	missense	USP42	GRCh38.p7	7:6156918	TGGAGACTGTCGCCC[A/G]GTTCCGGAGAGCCCA	84132
rs377244559	snp	C/T	0.000155988	0.00883004	intron-variant	USP42	GRCh38.p7	7:6142910	TGCGGTGATGTGGTG[C/T]TTGTGCCTCTTCTCT	84132
rs377259191	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114479	ATTATCTCAAATCCA[A/G]TACTTCATCTTTCAC	84132
rs377304826	snp	C/G	1.79062e-05	0.00299212	missense	USP42	GRCh38.p7	7:6153992	ACATCGTGGGGGACA[C/G]AGCACCCCCTGACCT	84132
rs377309106	in-del	-/AC			intron-variant	USP42	GRCh38.p7	7:6083678	GAGATATGTATATAT[-/AC]ACACACACACACATG	84132
rs377363946	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6088625	TCATCCTGCCAACCC[C/T]GATTGACGTCACTAC	84132
rs377447920	snp	C/T	9.94612e-05	0.00705129	synonymous-codon	USP42	GRCh38.p7	7:6147805	CGGCCAGTCCTCTCC[C/T]CGCCCCGTCATCAGT	84132
rs377506977	snp	C/G/T	7.0697e-05	0.00594512	missense	USP42	GRCh38.p7	7:6154037	GCTTAACAGGCGATG[C/G/T]GAGCCCGTTGTCCCA	84132
rs377512021	snp	C/T	0.00137384	0.0261731	synonymous-codon	USP42	GRCh38.p7	7:6145569	TATGTCTCAACCCAA[C/T]GGAGAGCCAATTGTC	84132
rs377551028	snp	A/G			missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115380	CATCTGAGAAGATTT[A/G]TCTTAAGTGGCAACA	84132
rs377554552	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094085	GACGGGGTTTCACCA[C/T]GTTGGTCAGTCTGGT	84132
rs377555571	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6137490	CAGCCTCCCAAGTAG[C/G]TGGGATTACAGACGT	84132
rs377566217	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6160338	AGGAGGCATCTGGGG[C/T]GGGTGGTGGCCGGGC	84132
rs377570802	snp	A/G/T	0.00106656	0.0230707	missense	USP42	GRCh38.p7	7:6154310	GGGACGCTGAGCCTA[A/G/T]CCCCGGCGAGAGGGT	84132
rs377573018	snp	C/T	3.31417e-05	0.00407059	missense	USP42	GRCh38.p7	7:6147824	CCCGTCATCAGTCAG[C/T]GGGTTGTCACCAACA	84132
rs377573972	snp	A/G	0.000437904	0.0147905	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104454	GCAAGGTAGTTGCAG[A/G]GGGCGAAGCCCACGA	84132
rs377635002	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6145256	CAATCACTTGAACCC[A/G]GGAGGCGGAGCTTCC	84132
rs377663785	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131854	GAGGAATAGAAAACT[A/G]CCTCTATTCCGTCTC	84132
rs386409441	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6133892	CATGTTTCTTCTTCT[-/T]TTTTTTTTTTTTTTT	84132
rs386709804	multinucleotide-polymorphism	CG/GA			intron-variant	USP42	GRCh38.p7	7:6101366	TGAGCCTTCGGACTT[CG/GA]GGGTGGGGCACTTGG	84132
rs386709805	multinucleotide-polymorphism	AG/CC			intron-variant	USP42	GRCh38.p7	7:6120442	GAGATGGGGTTTCAC[AG/CC]TGTTGGCCAGGCTGG	84132
rs386709806	multinucleotide-polymorphism	GA/TT			intron-variant	USP42	GRCh38.p7	7:6122788	TTTTTTTTTTAAATA[GA/TT]GATAGGGTCTCACTA	84132
rs386709807	in-del	AAGGCAGAGTGATCTC/TGAT			intron-variant	USP42	GRCh38.p7	7:6160426	CTCAGGAAGGCAGAG[AAGGCAGAGTGATCTC/TGAT]CTCAAGGAAGAGCTT	84132
rs397717212	in-del	-/C	0	0	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081359	ACCGGGGGCCGGGCC[-/C]GCCGCGGGGAGGTAG	84132
rs397799754	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6158942	GGCCACCACACAGAC[-/A]ACGCCTGACCACAGC	84132
rs397817822	in-del	-/A	0	0	upstream-variant-2KB	USP42	GRCh38.p7	7:6076889	AGACTCTGTATCAAG[-/A]AAAAAAAAAAAATTG	84132
rs397888967	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6141576	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAATAA	84132
rs397890563	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6111620	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	84132
rs397890870	in-del	-/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6078618	CTTGGCTTAAGCTAT[-/T]TTTTTTTTTTTTTTT	84132
rs397936885	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6085299	AATTTTTTTTTTTTT[-/T]AGTTTTTAGTAGAGA	84132
rs397957423	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6096943	TTTCTTTTTTTTTTT[-/T]GAGACAGTCTTCCTC	84132
rs398003534	in-del	-/T	0	0	intron-variant	USP42	GRCh38.p7	7:6090314	ATATATATATATTTC[-/T]TTTTTTTTTTTTTGA	84132
rs398003535	in-del	-/G	0	0	frameshift-variant	USP42	GRCh38.p7	7:6153884	CCGGGATCGCGGGGC[-/G]GCGGAGCCTTCTTGG	84132
rs398066574	in-del	-/AA			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103754	AAAAAAAAAAAAAAA[-/AA]CAAAACTTAAAAAAT	84132
rs398111002	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6142241	TTTTTTTTGAGACGG[-/G]AGTCCTGCTCTGTCA	84132
rs527272367	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6078098	GTGAGCCGAGATCGT[A/G]CCATTGCACTCCAGC	84132
rs527315958	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118854	ATCTATTTCTGGACT[C/G]TATTATGTTGTACTG	84132
rs527385127	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122901	TGATCTTGGTTCGCC[A/G]CAGCCTCCACCTTTC	84132
rs527386056	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118426	ACTTGGGAGACTGAG[G/T]TGGGAGGATCACATG	84132
rs527435775	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140021	TTCCATGGCTGTCCT[G/T]TTTGAATTCTTGATC	84132
rs527469093	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101877	TGAGGCCAGGAGTTC[A/G]AGTCCAGCCTGACCA	84132
rs527479702	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094813	TTCCACTTGGCTTTT[A/T]TTTTTTTTTGGTCAC	84132
rs527496472	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6139299	GGAAGCACACAGAAC[A/G]GTGTTCACTTTACCT	84132
rs527532761	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101224	CAGCAGACAAGGGAT[A/G]GAAGCATCCGCCAGT	84132
rs527542171	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107809	AAACTGTATTTGGAG[G/T]ATAAGGCTCAAGCTT	84132
rs527654661	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099505	AGGCGTGAGCCACTG[C/T]GCCTGGCCAATTTTT	84132
rs527742625	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106115	GATCAGTTTCACTTA[C/T]TTGTTTTAAATTAGG	84132
rs527748372	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6111945	TTTAAGAATAAACTT[C/T]ATCTTGGTGAGAATT	84132
rs527814862	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148645	GAACAGTAGTGAGCT[A/G]GTGTCACAAGGAACA	84132
rs527843351	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6122575	TCATGGGTTCAAGCG[A/G]TTCTCCTGCCTCGGC	84132
rs527875332	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088072	TGGGAGGCCAAGGCA[C/G]GAGGATTGCTTGAGG	84132
rs527889516	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6093921	TTTAAGATGGAGTCT[C/T]ACTCTGTCACCCAGG	84132
rs527910849	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6083341	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	84132
rs527922884	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161902	GCTGTTCCTTCATGC[A/G]AGCTGTGGGAGTATA	84132
rs527924770	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157579	AATTTTGTGTTTTTA[A/G]TAGAGACGGTGTTTC	84132
rs527943602	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093229	TTCCTTCCTCCCTCC[C/G]TCCCTCTCTTCCTCC	84132
rs527954405	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127079	GCATTTCCCTAATGC[G/T]TAAAGGTATTGAACA	84132
rs527963094	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161379	TCCTGCATCAGGAGA[C/T]GGAGTGGGGAAAACT	84132
rs527974957	in-del	-/TTC	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6127128	TGCCATCTGTTTGTG[-/TTC]TTTGGTGAAACGTGC	84132
rs527995235	snp	A/C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107655	TTCAGGTGATCTGCC[A/C/T]GCCTCGTCCTCCCAA	84132
rs527996037	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081338	CCCCACCGGTCCCCA[A/C]CATCATACCGGGGGC	84132
rs528019103	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132785	CACGCCATTCTCCTG[C/T]CTCAGCCTCCTGAGT	84132
rs528032937	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114455	AGCACCTCCTTATCT[C/T]CCCACGACATTATCT	84132
rs528056889	snp	A/G	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6126157	TGTTACGTGAATTAT[A/G]TAGTATGTAACCTTT	84132
rs528069737	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086307	GCCTCCTGGGTTCAC[G/T]CCATTCTCCTGCCTC	84132
rs528075244	snp	C/T	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6092075	CTTCTTCTTCTTCTT[C/T]CTCTTCCTCTTCTTC	84132
rs528075408	snp	C/T	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6160533	CCTCCAACTCACTAA[C/T]CCTGCGCCTCTTGTC	84132
rs528079279	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133419	TGTTTTATTATGGAT[A/G]TTTTCTACCCATAAT	84132
rs528112306	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160224	GTGGATTAATTGGCC[A/G]TTAATTAACAGGCTT	84132
rs528139632	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6097871	CTGGGACTACAGGCG[G/T]GAGCCACCGCGCCCG	84132
rs528154493	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131662	TGTTGGGGCTTCCAG[C/G]TTGCTGACTTTAGCT	84132
rs528161461	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6155962	GGATCTCACTATGCC[A/G]CGCACGCTGTTCTCA	84132
rs528214778	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136525	CTATTAAAAATCAAT[A/G]TGTTAAAATAATTGG	84132
rs528232451	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6131215	AACATCATAATAATT[C/T]TTACAATTCCAGCAG	84132
rs528284724	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148289	TTGCAGTGAGCTGAG[A/G]TTGCACCACTGCACT	84132
rs528297241	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153197	AGAATCGCTTGCACC[C/T]AGGAGATGGAGGTTG	84132
rs528336042	snp	A/G	0.000101097	0.00710902	missense	USP42	GRCh38.p7	7:6156936	TCCGGAGAGCCCAGG[A/G]TGGCTTTCCTCTCTC	84132
rs528346707	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6121324	GTTTGATGCTTGAAT[A/G]TTAAACCAACCTTGC	84132
rs528384700	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121980	TTTCGTTTGATCAAT[A/C]TGACCAGAAGTTTTT	84132
rs528398756	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6126540	TCTGCCCGCCTCAGC[C/G]TCCCAAAGTGCTGGG	84132
rs528407226	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6117321	TTCTCATATTATCTC[A/G]CTTCTTTCACTCAGC	84132
rs528408075	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6135069	TGCTGAGATGATAGG[C/T]ATGAGCCATGGCGCC	84132
rs528446269	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6079315	TACAAAAAATTAGCC[C/T]GGCGGGGTGGCACGT	84132
rs528450165	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159859	TCCCCAGCACAGGCA[C/T]CTCACTCAGGAGAGC	84132
rs528457923	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6146812	TGGTGGCTGACAAGG[A/G]TGGGCTTCTGCTGCG	84132
rs528513448	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6120844	CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC	84132
rs528544910	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155559	GTGTTAATATTCTTA[C/T]TTGTCAGATGTAGTT	84132
rs528618270	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142814	GCTTGAGCCCAGGAG[A/G]TCGAGGCTGCAGTGA	84132
rs528673568	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105541	GCCGGCCTCCCCGCC[C/T]CCACTGCATCCCTAA	84132
rs528679030	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6121159	TTGCTGTTTTTTTCT[A/T]GTAAAGAGACCTCCA	84132
rs528691465	in-del	-/AC			intron-variant	USP42	GRCh38.p7	7:6140807	ATTGATAGAAAAATT[-/AC]AGTTAAAAAATTTTA	84132
rs528749439	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6138115	GTCATGAAGTTGTCA[A/C]GTTTGTAGGTCTAAA	84132
rs528788945	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147314	CAGAAAATAAAAAAA[G/T]GAGCCAGGCGTGGTG	84132
rs528896370	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108806	AAAAAATTTTTTAAG[A/G]CCATTTCTACTCCAG	84132
rs528897524	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6102273	GTGCCATCACCACAG[C/T]CAACTGATTTTTGTA	84132
rs528906634	in-del	-/TCTGGAACTCCTGACCTCAGGTGA			intron-variant	USP42	GRCh38.p7	7:6087247	TGTTGGCCAGGCTGG[-/TCTGGAACTCCTGACCTCAGGTGA]TCTGCCCGCCTTGGC	84132
rs528940969	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152236	AGTGCGGCCGGATGT[C/T]ACCATACTCGGTGCC	84132
rs529007419	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113621	TGGTTTTTTTTGTTT[C/T]TGTTTTTGTTTTTTT	84132
rs529027027	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130315	TGGGAATTGGGGATC[A/G]TTGTCCCTGCTGGGT	84132
rs529029173	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6145739	GGGTAGGGAGAGGTG[C/G]AACTTTTACAGTTAA	84132
rs529058009	in-del	-/AAAC			intron-variant	USP42	GRCh38.p7	7:6108198	TCTCAAAACATAACA[-/AAAC]AAACAAACAAAAAAA	84132
rs529069538	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6128471	ATGCTTGCATGACAT[A/G]TCTTTTTTATCCTTT	84132
rs529071467	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6090736	ACAAAAAAACAAAAC[A/T]AACTATATATATATT	84132
rs529083596	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096653	GAAACAGGCTGATTG[C/T]ACAAGTTGATTAATC	84132
rs529093930	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084251	AGGCTGGTCTTGAAC[A/T]CTTGACCTCAGGAGA	84132
rs529095814	snp	C/T	1.65831e-05	0.00287945	intron-variant	USP42	GRCh38.p7	7:6159409	GCCCTGGCGATTTTG[C/T]AACCATCATTAAAAT	84132
rs529130162	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129887	AAAAAGGTTTCTTTT[A/G]TATACATTTAGAACC	84132
rs529136618	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159077	TGCCCGGCCCCGCCT[A/C]ACCCAGCGTCCTGTG	84132
rs529150315	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6095973	TCTTACTGTGCTCAG[A/G]TTGGTCTCGAATTCC	84132
rs529159408	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135299	TTAAACTCTCTGAGC[C/T]TTTTTCCTTTCTTGT	84132
rs529175461	snp	C/G/T			intron-variant	USP42	GRCh38.p7	7:6156548	TCAATCTCCTGGGCT[C/G/T]AAGTGATCCTCCTGC	84132
rs529190453	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6156432	GGCCCTGGACTGAAA[A/C]AGTCATTACAGTGAA	84132
rs529222754	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6124426	GTGCACCACCACACC[C/T]GGCTAATTTTTGTAT	84132
rs529228271	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134747	ATCTGTGGCCAGCAA[C/T]GCCAGAGTATTTACA	84132
rs529243936	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088763	GAGTTCGACATTTTG[A/C]TCTCCTTCTCTCCTG	84132
rs529269019	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158237	GGCTTCGCTGTCACT[A/G]CCTGGCAGAGGTGAG	84132
rs529294906	snp	C/G	0.00206611	0.0320747	intron-variant	USP42	GRCh38.p7	7:6139222	GAGCGCCAGCCATGT[C/G]TTCATTGGGGATCTC	84132
rs529300569	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6087460	TCCCACCTCAGCCTC[C/T]TGAGTAGCTGGGACT	84132
rs529354192	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101162	TTCAGCTAAGAACAG[C/G]CTCAGGAGAAGAGGC	84132
rs529426820	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6109381	CTCCTGAAAGGTGTT[A/C]TTTCTTCCTTTCCTT	84132
rs529442765	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077419	TCTTACTCTCTCCCT[C/G]TTTCATCTGTTGCCC	84132
rs529459924	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083127	GTGGGGTTTCACCAT[G/T]TTGGTCAGGCTGGTC	84132
rs529476201	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077067	TTTAGTAGAGACGGA[A/G]TTTCACCATATTGGT	84132
rs529503554	snp	C/G	4.96931e-05	0.00498439	synonymous-codon	USP42	GRCh38.p7	7:6150462	CAAAATCTTAGAGAC[C/G]TTCAGGCTTAGCAAC	84132
rs529510326	snp	A/G/T	0.000332055	0.0128812	missense, stop-gained	USP42	GRCh38.p7	7:6154696	GGCTGGGGCCGGGAG[A/G/T]AGTTCTACCCCGACA	84132
rs529520174	snp	A/C	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6154408	AAGGTGGACCGAGGC[A/C]ACTACCGCAGCCGGA	84132
rs529569119	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6082274	GCTGGGACTACAGGT[A/G]CCCGCCACCAGGCCC	84132
rs529573020	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089398	AGGGGGAGTTTCTTT[C/T]AGGCCAGCAAGCTTT	84132
rs529612042	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123740	ATAGTCTTAGCTACT[C/T]GGGAGGCCGAGGTAG	84132
rs529624847	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129216	GACGTATAGAAACAT[G/T]ACTTCCCTATGTCCT	84132
rs529661004	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6153702	TTGTAATGCAATGAC[A/G]TGAGCCTGTCAAGCC	84132
rs529691533	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117822	ACCTCTTTTCTTTTT[C/T]GTTTTGTTTTTGTTT	84132
rs529711199	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081391	TGGCGGGCGGCGCAG[C/T]CACAGCCCCGGCCCC	84132
rs529713306	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098339	TCTCTTATCTGCTCC[C/G]CAGCCCTCACCCCTC	84132
rs529713636	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157558	GCCCGCCACCACGCC[C/T]GGCTAAATTTTGTGT	84132
rs529725694	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6122862	GTCTTGAACTGCTGG[C/T]GCCCAGGCTAGAGTG	84132
rs529751307	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6122514	CTTGCTCTGTTGCCA[C/T]GCTGGAGTGCAGTAG	84132
rs529799288	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6098646	AACCTCCGCCTCCCC[A/G]GTTCAAACGATTCTC	84132
rs529808717	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6122172	GGAGTCTTAGGTCAT[A/T]TGATTTGAGATCTTT	84132
rs529823262	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080528	GATCATTTGAGGTCA[A/G]CAGTTGGAGACCAGT	84132
rs529956643	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6107143	TTTGGTTGGTTTTTC[C/T]ACAGTTACAATGCTG	84132
rs529968480	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6149268	AACCCAACCAGGTAG[C/G]AAGTGTGTGACTCCA	84132
rs529975932	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112533	GTGGTTACATTCGTT[A/C]AAACTCATCCAGATA	84132
rs529995797	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6119288	CTGTAGCCTGGGCAA[C/G]ATTGTGAGACCTCGT	84132
rs530001650	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143343	CTGCCAAATAGCATT[G/T]TCATTGACTTTCTTA	84132
rs530023386	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118388	TTATCTGGGCTTGGC[A/G]GTGTGCGCCTATAGT	84132
rs530023808	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106054	ACATTTTAAACCTAA[C/T]TCTTTTTACTTTGTC	84132
rs530028408	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6123167	TCGTTACCATTTATG[A/G]AATGACCCTCTTCAT	84132
rs530032276	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144330	ACATTTGGGCTTCAT[C/T]GTCTGTTTTGTTGGT	84132
rs530062840	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136669	AATGAATACTTTACT[A/T]TACGCAGTGACAGAA	84132
rs530081113	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6111458	TTCAGAGAGGGGCTT[A/G]TTTTGCAAGGCGTGA	84132
rs530084292	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6098104	AGAGACGGGTTTCAC[C/T]ATGTTGGCCAGGATG	84132
rs530093150	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110752	ACTGTGTATAATTTT[C/T]CTAGTTTTAAGCAGT	84132
rs530109547	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6144591	AATTAAATAATCGGC[C/T]GAGTGTGGTGGCTCA	84132
rs530138731	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148167	CCAGGGTGAAACCCC[A/G]TCTCCACAAAAAATA	84132
rs530150564	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6105621	CCTGGCTGCTCCGTG[G/T]AGAGTCCGAGGTGCC	84132
rs530155821	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6116140	CTGATGCCAGCAACT[C/T]GGGACAGGCGAGGTT	84132
rs530156322	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6115708	GAAAAACATTTTGCA[C/T]CTAATTAGACCTGTG	84132
rs530200944	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6132757	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAC	84132
rs530212786	in-del	-/AAA	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6148359	ACCCCCCAAAAAAAC[-/AAA]AACCCCAAAATATAC	84132
rs530309193	snp	C/T	9.33053e-05	0.00682964	missense	USP42	GRCh38.p7	7:6157034	AGGGATGACAGGTGT[C/T]GTCTCTTTGAGTATG	84132
rs530309477	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086826	CTGTCTCCCAGTTCA[A/G]GCAATTCTCCTACCT	84132
rs530309526	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093183	TCCTTCCCTCCCTCT[C/T]TCCCTTCCTTCCTTC	84132
rs530312234	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6132224	CCACCACACCTGGCC[C/T]GTTCTTTTTCTTTTA	84132
rs530320531	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092729	AAGGAGAGATTTGGG[A/G]TCTGTCTCCTAAAAA	84132
rs530321366	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6099455	TCCTGACCTCATGAT[C/G]TGCCCGCCTCGGCCT	84132
rs530351761	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6160665	ATACTGTACAGATTT[C/T]ACCATGGAGAACTTT	84132
rs530370986	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137232	CTGAAGATTAAAGAG[A/G]TCTTATATTGGCCCT	84132
rs530402647	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137842	CTTGCCACTACCCCT[C/G]GCTAATTTTTGTATT	84132
rs530409630	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6091571	ATTATACTATAATTG[A/G]GTTTCTATTGATTAT	84132
rs530413970	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131602	CCTCATCCTTTGGCT[A/G]GAGAGAGTGGGAGCG	84132
rs530424792	snp	A/G			intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153413	GGAGCTGGGCTTGAT[A/G]ATATAACATTTTATT	84132
rs530427799	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6090942	GTCAGCAATTTATGT[C/T]CCAGGAAGAATTTGT	84132
rs530519056	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159875	CTCACTCAGGAGAGC[A/G]GAGCCTTGCTCCCTC	84132
rs530594135	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6151437	AAAAATAACTTCTTT[C/T]TTTGTTTGTTTTTTT	84132
rs530594494	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096903	TCTGACACTCCAGGA[C/T]GCCATCATTTTCTTT	84132
rs530628170	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6086266	GCTGGAGTGTAGTGG[C/T]GCGATCTCAGTTCAC	84132
rs530631394	in-del	-/AAT	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6151294	TCAATTTGTTAAAAA[-/AAT]TGATTTCTTCAATAG	84132
rs530635887	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156617	ACCATACCTGGCCTA[C/T]GTGGCTAATTAGATA	84132
rs530639628	snp	C/T	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6119925	CAGGCTGGTCTTGAA[C/T]TCCTACGCTTAAGCG	84132
rs530654748	snp	A/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114354	TTTTTTAAATGTTCA[A/T]AGTGGATATAAAAGA	84132
rs530668113	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135528	ATGGTGGCGCATGTA[C/G]TAGTCCCAGCTACTT	84132
rs530671281	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160212	AGTGAAGAGTCTGTG[G/T]ATTAATTGGCCGTTA	84132
rs530688315	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6085804	ATTTTTAGTAGAGAC[A/G]GGATCTCACCATGTT	84132
rs530690748	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103037	CAGGGGAGGGAAAGA[A/G]GCAGTGAGAGAGGAA	84132
rs530705124	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6152529	TGCCCTCACTGAGGC[C/T]CTCTGTTAGGAGGGC	84132
rs530739245	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6132764	GCAACCTCCGCCTCC[C/T]GGGTTCACGCCATTC	84132
rs530743816	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079372	CTGAGGCAGGAGAAT[A/C]GCTTGAACCCCGGAG	84132
rs530770926	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6088456	AGAGACGGGGTTTCA[C/G]CACATTGGCCAGGCT	84132
rs530789263	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156146	GTAATTTTAGTTGAC[A/G]TCTCTTGAAACTGAA	84132
rs530792867	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155527	TGAACAATTGGGAGT[C/G]TTTGACCTTAGAATT	84132
rs530829287	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121074	TTTATAGACGCAACT[A/G]TGTGATACGTGAATA	84132
rs530882351	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083577	ACATATATATGTATG[C/T]ATACATATATATACA	84132
rs530901597	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6119422	ACTGCAGTGAGCCAT[C/T]ATTGTGCAGGTACGC	84132
rs530914733	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124025	GGATTACAGACATGC[A/G]CCGCCGTGCCCGGCT	84132
rs530919397	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129770	GGAGGCTGAGGCAAG[A/C]GAATCACTTGAACCC	84132
rs530934328	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6078157	AAAAAAAATAAAAAA[C/T]AAAAAAAAATAAGCC	84132
rs530966788	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119998	TGAGACGGAGTCTCG[A/C]TCTGCCGCCCGGGCT	84132
rs530995640	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089809	GTGCTGGGATTACAG[A/G]TGTGAGCTACCGCGC	84132
rs531014480	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6136423	AATTTTTAGTAAAAC[A/G]TTTGCTATATAAACA	84132
rs531029858	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6124424	GGGTGCACCACCACA[C/G]CCGGCTAATTTTTGT	84132
rs531129773	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6120494	GTGATCTGCCCGACT[C/T]GGCCTCCCAAAGTGC	84132
rs531143064	snp	A/T	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6146338	AATATTCAGTGTTTT[A/T]AAAAAAAAAAAAAAC	84132
rs531145164	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6078787	AACTACTTCTGCTTT[C/G]TTCTTTACTTCTCCA	84132
rs531170082	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6139390	ACACGTGTGTCTTAC[C/G]TAACAGTTTGAGTTG	84132
rs531170221	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096730	GTCTGCTTACAATGA[C/T]ATATACTGTGCTTTT	84132
rs531172313	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109333	AATGTGAAGTCCAGA[C/T]ATTAAGATGTTGTGC	84132
rs531230593	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145135	TCAGGCGTTCAAGAC[A/C]AGCCTAGCCAAGATG	84132
rs531238868	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6107904	ATTGAAATTGACAAA[C/T]ATCTTTTCTATTTCT	84132
rs531251862	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114148	ATAGCCTGAGTTCAA[A/C]ACCTGCTTCCTTAGT	84132
rs531297082	snp	A/G/T	7.53097e-05	0.00613589	intron-variant	USP42	GRCh38.p7	7:6145696	ACTATTGTTACATAC[A/G/T]TGCTATAAGACAGCA	84132
rs531298604	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6113124	TGGCCAGGCTGGTTT[A/C]AAACTTATAATCCAC	84132
rs531310305	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118978	TCAGTGTTTTGGGAG[G/T]CTGAGGCAGGAGGAC	84132
rs531377448	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134609	CTGTCCGGTGCATTC[A/G]AGGCTGTTGAGCGGC	84132
rs531399504	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158659	ACTGCCGGTGAGGAC[A/G]GGTTGCCTGCGGGCC	84132
rs531427317	in-del	-/CTC	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6119925	CAGGCTGGTCTTGAA[-/CTC]CTACGCTTAAGCGGT	84132
rs531451165	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6078430	ACACGGTGAAACCCT[A/G]TCTCTACTTAAAATA	84132
rs531466230	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6076961	CTCACTGCAACCTCT[A/C/G]GCTCCCAGGTTCAAA	84132
rs531488241	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134277	TTTTAAAGTTATTGT[C/G]TTCTGATTATATTTT	84132
rs531517132	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089513	CTGACCCTGGACCCC[A/G]TCCCTGCTTCACCTG	84132
rs531521127	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6148943	CTGTTTTTGTTTTTA[C/T]CATGAAGCTTTCCAG	84132
rs531535888	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146550	GGGCCTGTGGTCTTA[C/T]CTGCTCCGAAAGTTG	84132
rs531580092	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093984	AACCTCCACCTCCCG[A/G]GTTGAAGTGATTCTC	84132
rs531590756	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6102068	ACCTTAATTCACAAA[A/T]AATACCTTTTCTATT	84132
rs531600513	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6162057	CAGACCTAACTTCTC[A/G]GCAAAGCATATCTAT	84132
rs531610092	in-del	-/T	0.281313	0.248031	intron-variant	USP42	GRCh38.p7	7:6128257	TGTGCCTGGCCCTGC[-/T]TTTTTTTTTTTTTTT	84132
rs531681225	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140278	AGGGTTAGTCCTACT[A/G]GGAAGGAAGGAAAAG	84132
rs531683072	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6084078	GTCACCCAGGCTGGA[A/G]TGCAGTGGCTCAATC	84132
rs531688523	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6108987	GATGTGAATAAGAAC[A/G]TGGTAGAGAACAGCA	84132
rs531734077	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6106539	TGTGAAGTCTCATTC[C/T]TCCACACAGATCCAA	84132
rs531769086	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6107914	ACAAACATCTTTTCT[A/G]TTTCTACTTGAGTTC	84132
rs531794759	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088736	TTTCTCTTTCCACCA[A/T]CTCATCAAGGTGAGT	84132
rs531824613	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081604	TTCTCCTTTCCGACT[A/G]GGCAGGCGGGGCAGG	84132
rs531825302	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6138621	GCCGTAGACTGGTAC[A/C]CAATGTGGCCTGTTA	84132
rs531880819	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088189	TGCTCCAGTGCACTC[C/T]AGCCTGGGCAACAGA	84132
rs531883560	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144639	CTTTAGAAGGCCTAG[G/T]TGGGCATATCACTTC	84132
rs531888276	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138003	TATTTTTATACATAT[G/T]TATATAGCAGACATG	84132
rs531932965	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6082198	CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC	84132
rs531949929	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158194	GCTTGATTGGGGCGC[A/G]GCCAGGTGCGTTCCC	84132
rs531958966	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153252	CGCTCCAGCCTGGGC[A/T]ACAGAGTGGGACTCT	84132
rs531959070	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6157490	GCAACCTCTGCCTCC[C/G]AGGTTCATGCTGTTC	84132
rs531963905	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6093953	TGGAGTGCATGGCGC[A/G]ATGTGGGCTCACTGC	84132
rs532006383	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080418	GGTTTTTGTGTAAAA[G/T]AATTACTTAAAAAAA	84132
rs532029090	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128546	TGTAAACAGCGTATC[A/G]TTGGGTTGTGCTGTT	84132
rs532147803	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132156	GTCTCGAACTCCTAG[A/G]CTCAAGCGATCCACC	84132
rs532201878	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086406	GAGATAGGATTTCAC[C/T]GTGTTAGCCAGGATG	84132
rs532219645	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6092550	ACTTCAGGGGTAAAC[A/C]CATCCACTAAGTATT	84132
rs532402643	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152518	GCGGGTGGGAGTGCC[C/G]TCACTGAGGCCCTCT	84132
rs532425553	snp	A/G			missense	USP42	GRCh38.p7	7:6154688	GCGAGCGTGGCTGGG[A/G]CCGGGAGAAGTTCTA	84132
rs532429788	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6111577	TGTTTTTAGTTGCTA[A/G]AATATTATTAGTTTC	84132
rs532462029	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115279	TTTATTTAGCTTCAG[C/T]ATGCAAAGCTTGGTT	84132
rs532462789	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6160039	TGTGGGGCTTTGTTG[-/A]GATCACTTCACACAG	84132
rs532473144	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148310	CCACTGCACTCCAGC[C/T]TGGGCAACAGAGTGA	84132
rs532487414	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6145190	ATACAAAAATTAGCT[C/G]GGCGTGGTGGCGCAC	84132
rs532516697	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6143507	GTTTCCACATGAAGT[C/G]AAGAGTGCCTATTTT	84132
rs532522017	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137185	GTGTAATTATACAGT[A/G]ACAAACTGTAATCTT	84132
rs532563720	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147327	AATGAGCCAGGCGTG[A/G]TGGTGCATGTCTGTG	84132
rs532571955	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109979	ATGCTGGGATTACAG[A/G]TGTGCACCACCATGC	84132
rs532618687	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6139904	CCTTCCTGACAGACA[A/C]AGCTCCCACAGCTCT	84132
rs532635083	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6098644	GCAACCTCCGCCTCC[C/G]CGGTTCAAACGATTC	84132
rs532641591	in-del	-/CATGATG	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6121365	TGACTCACACTTGGT[-/CATGATG]CATTATTCTATGTAT	84132
rs532678083	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152226	GACAGCTCAGAGTGC[A/G]GCCGGATGTCACCAT	84132
rs532692166	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6101211	GCGAACACCACAGCA[A/G]CAGACAAGGGATGGA	84132
rs532692424	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131765	TCCGTAGCATGTCTC[C/T]TTCTCTTTCTACCTT	84132
rs532709929	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110661	TAAGCACAAAATTAA[A/G]TCTAGATTTTTTCTG	84132
rs532716253	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142864	ACTCCAGCCTGGGTG[G/T]CAGGGCAAGACCCAA	84132
rs532727835	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160254	TTATCAATGTGTCCT[C/T]AAGGGAGAGGCCCAA	84132
rs532861308	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104667	GCCCTTTCGCCGGCG[C/G]GCAGACGCGCGACCA	84132
rs532884234	in-del	-/TGAAGC	0.0107246	0.0724382	intron-variant	USP42	GRCh38.p7	7:6158367	GTTTGTGTTCACGTG[-/TGAAGC]TGAAGCGCATCCCCT	84132
rs532908313	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135387	GGGTGGTGGCTTACA[C/G]CTATAATCCCAGCAC	84132
rs532910633	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6146608	AGGCCGAGGCTGCAG[C/T]AAGCCATGATTGAGC	84132
rs532938602	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6111867	ATCCACCCACCTCAG[C/T]GTCCTGAAGTGCTGG	84132
rs532969162	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130734	GTCTTTTGTATTCTT[C/T]TATGAGATGGTTGCT	84132
rs532972295	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134826	GGTCTCGCTCTGTTG[C/T]CCAGGCTGTAGTGCA	84132
rs532972578	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141538	ACTAGATTTTCTATA[C/T]TAGCCAAGTACAGTT	84132
rs533066491	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6127303	TTTTGGTGAAGTTCA[A/G]TTGGTCAGCCTTTAG	84132
rs533083979	in-del	-/T	0.234401	0.249513	intron-variant	USP42	GRCh38.p7	7:6106732	ACCACACCCAGCTAA[-/T]TTTTTTTTTTTTTCT	84132
rs533087797	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141205	CTTTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTT	84132
rs533114447	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6086122	CTCATTGCAACCTTC[A/G]CCTCACAGGTTCAAG	84132
rs533131980	snp	C/G/T	4.8968e-05	0.00494789	missense	USP42	GRCh38.p7	7:6154732	CGCTGGGACAGGTGC[C/G/T]GGTACTACCATGACA	84132
rs533135580	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156080	AATTGGTTGGTGATT[A/G]TCTTGAAAATGACGT	84132
rs533158277	snp	A/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6079066	ATAAGATGTAGGCAT[A/T]TCTTGAATTTTATTA	84132
rs533159968	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084946	CTGGTCTTGAACTCC[G/T]GACCTCAGGTGATTC	84132
rs533175287	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6155681	GCCCAGCGTAGGCAT[C/T]GGAGACACCTTCGTT	84132
rs533177313	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6159798	CCGGCTCACAGCGGC[A/G]GAGCCCACGGGCCTT	84132
rs533229464	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6090859	ATATATAACTAACTT[C/T]TATTAGTAATCCTCT	84132
rs533233767	snp	A/G	0	0	intron-variant	USP42	GRCh38.p7	7:6125035	AAAATACAAAAATTA[A/G]CCGGGTGTGGTGGCT	84132
rs533242093	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	USP42	GRCh38.p7	7:6088862	ACAATCAGTGCACCC[A/G]CAGGAGGGGACGGCG	84132
rs533300456	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6130400	GGTTTTGTTACCACT[C/G]AGTGATGGTGACAGT	84132
rs533308015	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128807	CATCATTTTGCTTTA[C/G]TTGAGTCTTTCTTTC	84132
rs533332407	snp	C/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6123877	TTTTCTTTTTCGTAT[C/T]GTTTCTCTTTTTTTT	84132
rs533365482	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	USP42	GRCh38.p7	7:6078090	AGGTTGCAGTGAGCC[A/G]AGATCGTGCCATTGC	84132
rs533445629	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6143874	TCAGAATTGTCCTAA[C/T]TTCCTTTCCTTTCAT	84132
rs533480915	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6087871	AATAACATACTTAAC[C/G]TCTAATCTGTAAAAT	84132
rs533485471	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083988	CTGGTTGTGTAGGTC[A/G]TCCGTGAGTTAAGGT	84132
rs533505154	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134126	TCGATCTCCTGACCT[C/T]GTGATCTGCCCTCCT	84132
rs533535112	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6138296	TTAGCTGTTTAATCA[A/G]TTAGAAACAGGACTG	84132
rs533544303	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144401	CTGAAATCCAAAGAG[G/T]ACTTCCTGCTAGACT	84132
rs533552290	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6158454	GCTGAGTTGTGGGTT[A/G]GGTGGAGCTGTGTGT	84132
rs533552429	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6133591	GCTATCATAGCTTAC[C/T]GCAGCCTCCAACTGC	84132
rs533572496	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151045	TGTGACTGCACTGGA[C/T]CCCGTAGGCAGCTGT	84132
rs533582543	in-del	-/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6119957	TCTCTTGCCTCAGCC[-/T]TTTTTTTGTTTTTGT	84132
rs533601553	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114025	AAGTTGTTTCTTGAG[C/T]TTCATCTTGAGTTCC	84132
rs533668493	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6124336	GCAGTGGCGCGATCT[C/T]GGCTCACTGCAACCT	84132
rs533672842	snp	G/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6119694	TAGGCCTTGTTTTTT[G/T]TTGTTGTTGTTGTTT	84132
rs533725850	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157976	GAGCTGTGAGCCTGT[C/T]AGAAGCGGATGTCAC	84132
rs533764994	snp	C/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6127531	CGTCATTTTCTTGAA[C/G]AAGCTGTCTTTGTTG	84132
rs533799240	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161709	CCCACCTCGGACGGG[C/T]AAAGGAAAATTGGAG	84132
rs533808443	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093439	TACAGGCATGCACCA[C/T]CATGCTCGGGTAACT	84132
rs533849236	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6148843	CTCCCCTTTTGGGCT[C/G]TGCTCCAGAGTGACA	84132
rs533860964	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138781	GGGATCCAGGTTCCA[C/T]GCTCCTTAGGAGAAT	84132
rs533871649	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106304	TGAGAACGTGGATTA[C/T]ATTGTTTACGAAGAA	84132
rs533875072	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112238	TGGATCACCTGAGGT[C/T]AGGAGTTTGAGACCA	84132
rs533887823	snp	A/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6117902	AAATGCCTGTTGAAA[A/T]CTTTTGCCCGTTTGA	84132
rs533925163	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6086510	GCGCCCAGCCTAGCC[A/G]GGCTAATTTTTGTAT	84132
rs533942557	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128054	TGGTCTCAAGCTATC[C/G]TCCTGCCTCAGCCTT	84132
rs533973801	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6122119	CATTTCTTCTGCTTA[C/G]TTTGGATTTAATGTG	84132
rs533985794	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6092263	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	84132
rs533991712	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098160	CTTCCACCTTGGCCT[C/T]CCAAAGTGCTGGGAT	84132
rs534041295	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094152	CTCCTGAAGTGCTGG[A/G]ATTACAGGCATGAGC	84132
rs534041970	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100569	TCCTGACCTCAGGTT[A/T]TCTGCTCATCTCAGC	84132
rs534050738	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105680	GGAGAGGAGAAGCCG[C/G]GTGGCGCGTCCCCAA	84132
rs534098470	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117320	ATTCTCATATTATCT[C/T]GCTTCTTTCACTCAG	84132
rs534102409	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099770	GATTTCAAGAGCAGC[C/G]TTGCCAATATGGTGA	84132
rs534165465	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153417	CTGGGCTTGATGATA[C/T]AACATTTTATTTTTA	84132
rs534198750	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6122217	TAAGTGTCAAATGCT[A/G]TAAATTTCCCTATGA	84132
rs534211649	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160380	CGCCTCCCTGGCTGA[C/G]CTGCCCGCACCGCCA	84132
rs534277824	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6089107	TGGAGTGAAGTGGTG[C/T]GATCTCTGTTCACTG	84132
rs534309800	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6079393	AACCCCGGAGGCGGA[A/G]CTTGCAGTGAGCCGA	84132
rs534321906	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079234	GAGGCCAAGGCGGGC[A/G]GATCACAAGGTCAGG	84132
rs534322540	snp	A/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6097727	TCCCGAGTTGCTGTG[A/T]CTACAGGCGGCCGCC	84132
rs534323281	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6085855	CCTGACCTTGTGATC[C/T]GCCCGCCTTGGCCTC	84132
rs534349624	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6145193	CAAAAATTAGCTGGG[C/T]GTGGTGGCGCACCTG	84132
rs534357428	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156199	GCCATATGGAAAATA[A/G]GCAGTGGTTATTGGA	84132
rs534360676	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112529	AAATGTGGTTACATT[C/T]GTTAAAACTCATCCA	84132
rs534364286	in-del	-/AAT	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6079484	ATAAATAAATAAATA[-/AAT]AATAGTACTTAGTAT	84132
rs534381576	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6085138	TTATTTATTTATTTT[G/T]AGACAGATTCTCACT	84132
rs534385981	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159895	CTTGCTCCCTCGTCC[A/G]TCCCGTCCCCTGTGC	84132
rs534395413	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6110607	TATAATTATAATTTT[-/A]AAAAATATAATGTAT	84132
rs534402584	in-del	-/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6086705	TCCCCTTTCCTTTCC[-/T]TTTCCTTTTCCTTTT	84132
rs534428397	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6144489	ACACTGAATTTTCCC[A/G]TTTTCTTCCCACTTT	84132
rs534467158	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080103	TGGCGGACGCCTGTA[C/G]TCCCAGCTACTCGGG	84132
rs534469231	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157206	CCTGGTCTGGCCTCA[A/G]TGCTCATCCCTGCAG	84132
rs534494469	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6129501	GGTGGAAGTTGTGGT[G/T]AGCCAAGATTGTGCT	84132
rs534561207	snp	A/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6121133	CTGTGTAGGTTCTTT[A/T]TTAATTTTTCTTGCT	84132
rs534576309	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114933	CTGACCTCATAATCC[A/G]CCTGCCTCAGCCTCC	84132
rs534611715	snp	A/G/T	0.00517997	0.0506535	intron-variant	USP42	GRCh38.p7	7:6110260	AGCCTGGCTGGGAAC[A/G/T]CTGGACCTGGCTCTC	84132
rs534677147	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6116306	GCATTTGAGAACTTC[A/G]TCTTCAACCTACATG	84132
rs534690047	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141358	TAGGTGCATGTGCCA[C/T]CATGCCCAGCTAATT	84132
rs534699206	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146426	GCACTTTGGGCGGCC[A/G]AGATGGAAGGATCAC	84132
rs534709753	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140838	AAATTTCAAAATTGT[A/G]TTTTGTCATTTCAGT	84132
rs534711384	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6108530	TCTGTCGCCAGGCTG[C/G]AGTGCAGTGGCGCGA	84132
rs534746751	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125105	AGAATCGCTTGATCC[C/T]GGGAGTTGGAGGTTT	84132
rs534754421	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134671	CATCACTTAGCATGC[A/G]CTAAGAATGATTTTT	84132
rs534758855	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145898	AACAGGGTGAAACCC[A/C]GCCTCTATTAAAAAT	84132
rs534795919	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114297	GGCAGATGTTACAAG[C/G]AATCAAATGTATCTC	84132
rs534801099	snp	C/T	0.000201089	0.0100252	intron-variant	USP42	GRCh38.p7	7:6143053	CTTGATGCCGGCTTC[C/T]CCAGTGGGGATGGCC	84132
rs534812736	snp	C/G	1.6708e-05	0.00289028	missense	USP42	GRCh38.p7	7:6147892	CTCTCACATGATAAA[C/G]GTAACAGTCCTTAGG	84132
rs534897243	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6116680	AAGAATTTGGAAAGT[A/T]CAGAAAAACTTAAAG	84132
rs534935529	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6159336	GAGTGGCCTCAGGCG[C/G]TCACAGGGAACCGCA	84132
rs534944436	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6100678	TATTCTTGGTATCCA[-/CT]GTCTTTTTTTTTTTT	84132
rs534999707	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6136659	CAGTTTGGTGAATGA[A/C]TACTTTACTATACGC	84132
rs535036399	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128938	TGATCCTCCTGCCTC[A/C]GCCCCGCAAGTGGCT	84132
rs535055865	snp	G/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6109064	AGCACAGGGTGCTGT[G/T]GGGGCCTTGAGGAGG	84132
rs535062745	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134338	TTTTCTCCTTGTTAC[C/T]GGTCATTTCTGCATC	84132
rs535081729	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095403	GGCCGGGTGTGGTGG[C/T]TCACGCCTGTAATCC	84132
rs535122583	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108623	GTAGCTGGGATTACA[C/G]ACACGCACCACCATG	84132
rs535132451	in-del	-/CATA	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6151947	TGGTCTGTTGTTGAC[-/CATA]CGTATGTATGAGGTA	84132
rs535137697	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6146777	GCCATGAGCACTGAA[G/T]GTGCAGCTGCAGGGA	84132
rs535152069	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	USP42	GRCh38.p7	7:6078228	AAACTGTGGGAGAAA[A/T]GTTTCTGGGTAGTTA	84132
rs535189617	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107983	ACCCTAGTTAAAAAT[G/T]ACACCAGCCTGGCCA	84132
rs535249063	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6150785	GCGGTGTTACTGGCA[C/T]GCCTTCAAGTGCCAT	84132
rs535267752	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6122967	CAGCTGGGATTACAG[C/G]CATGCGCCACCACAC	84132
rs535275454	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096450	TCATCCTGCCAGCCC[A/G]TAGGTTGCATGTGAT	84132
rs535288055	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104097	TTTTCTTTTTTGAGA[C/G]AGACTCTCGCTCTGT	84132
rs535288929	snp	A/T	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6155163	AAAGAAGAAAAAGAA[A/T]TCCAAAGACAAACAC	84132
rs535306417	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6118093	TTATTCGTTGTGCTG[G/T]AGGTGTTTTAAGAAA	84132
rs535315171	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6092650	CAAAATAGTCTCTGG[A/T]AAGTAGGCACAGCAT	84132
rs535342024	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6124083	GTTTCACCATGTTGG[C/T]CAGGCTGGTCTTGAA	84132
rs535362068	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119297	GGGCAACATTGTGAG[A/G]CCTCGTCTTTACAAA	84132
rs535394639	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6158514	CCAGAGCCAGCATGC[A/G]TTGTTGATTGAGGGG	84132
rs535399188	snp	A/G	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6129411	AAATACAAAAGATTA[A/G]CCAGGCATGGTGGCG	84132
rs535445582	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081718	GAGAGGGTGATCGCG[C/G]TGCTGAAAGCCGACT	84132
rs535451113	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133879	TTTGCATCTATTTCC[A/G]TGTTTCTTCTTCTTT	84132
rs535455058	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118158	CAGCACTTTGGGAGA[A/G]CGAGGCAGGTAGATC	84132
rs535461752	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081217	CACCCCGTATACCTC[C/T]GCTTTAAGATGAGAG	84132
rs535484399	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101359	GATCCTGTGAGCCTT[C/T]GGACTTGAGGGTGGG	84132
rs535493131	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120251	TTACAGGCGTGAGCC[A/G]CTGCGCCCGGCCCTT	84132
rs535567857	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6139635	GCAGACTCAAGAGGA[A/T]GAACGAGGGGACAGA	84132
rs535572811	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6113182	TTACAGGTGTAGGCC[A/G]CTGCACCCGGACAAC	84132
rs535601029	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119808	TCCTTGGCTCAAGGG[A/G]TCCCCTTGCCTCAGC	84132
rs535602453	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6081890	TATATTCGTTAACAC[C/T]AACATATATAGAAAT	84132
rs535651187	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6083679	AGATATGTATATATA[C/T]ACACACACACACATG	84132
rs535665390	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6138965	GCTTATGTTAGTGCT[A/G]TTTCCTCATAAAGTA	84132
rs535675728	snp	C/T	0.000399281	0.0141238	synonymous-codon	USP42	GRCh38.p7	7:6154872	GGGCTGCGAGCCGGC[C/T]CGGGAGAGGGAGCGG	84132
rs535688395	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6113145	TATAATCCACCCGCC[A/T]CGGCCTCCCAGAGTG	84132
rs535711868	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6089587	TCCCAGGCTGGAGTG[C/G]AAGGGTGCGATCTCG	84132
rs535715904	snp	A/G	0.0107246	0.0724382	intron-variant	USP42	GRCh38.p7	7:6082632	TTTTTTTTTTTTGAG[A/G]CACTGTCTCCCTCTG	84132
rs535719829	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6123358	TGAGACCCTCTCTGT[A/G]TAATATAAAATATTA	84132
rs535746467	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112863	TGGCTTCGAGTAGTT[C/T]GATCGCCATGTTGTT	84132
rs535758269	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112405	AGTGAGCCCAAGATC[A/G]CACCATTGCATTTCA	84132
rs535798302	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6124003	GCCTCGGTCTCCTAA[G/T]TAGCTGGGATTACAG	84132
rs535864237	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6143558	TTTTAAGTAGATTTC[C/T]ACTTTGTGGTCAGGT	84132
rs535910519	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6148030	AATCAAACCCTCTTA[C/G]ACAGTATTTCAAATA	84132
rs535994783	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127385	CCTGCAGATTTTTTC[C/G]TATGTTAATTTTTTC	84132
rs536014952	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6087204	GCCCAGCTAATTTTC[A/G]TAATTTTAGTAGAGA	84132
rs536047995	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145226	ATCCCGGCTACTCGG[A/G]AGGCTGAGGCAGGAC	84132
rs536060073	snp	C/G	3.97772e-05	0.00445949	missense	USP42	GRCh38.p7	7:6150071	GGGGCTGGGCAAGGA[C/G]AATGGGATTGGTACG	84132
rs536069962	in-del	-/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6110628	TATAATGTATTTCAC[-/T]TGGTGCCATTTGCAC	84132
rs536091057	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6127961	AGAATCTTGTTCTGT[C/G]ACCCAGGCTTTGTGC	84132
rs536091458	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6160882	CAAGTTAGACATCTG[G/T]TGCAAGACCAACCGG	84132
rs536096246	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093026	GTGTCTGTTTCCAAA[C/G]AGTGCTCTCTGTGAC	84132
rs536100199	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136922	GGGATTACAGATGTG[C/T]ACCACTATGCCCAAC	84132
rs536157204	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118604	ACTTTCTTCTAGAAG[C/T]CTTAAAGTTTTAGCT	84132
rs536183481	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137722	TCTCACTCTGTCGCC[C/T]AGGCTGGAGTGCAGT	84132
rs536204081	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131446	GCCACTGCACTCCAG[C/G]CTGGGTGACAGAGTG	84132
rs536204184	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6099023	TCCTGACTTTGGTGT[C/T]AGAGACTGATAGTAG	84132
rs536250547	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6121447	AAGTATTATTAGCCT[A/G]TAGTTTCTTATAATG	84132
rs536270147	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6136336	TAATGTCCAACTGGT[A/G]AAAAAAACCGAACCC	84132
rs536280601	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105787	CAGATGTTGGAAATG[A/C]AAATTGGACGGAACA	84132
rs536288693	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6111583	TAGTTGCTAGAATAT[C/T]ATTAGTTTCTTTTAT	84132
rs536292466	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097683	GCAAACTCCGCCTTC[C/T]GGGATCATGCCATTC	84132
rs536293392	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096714	CCTGGAGATCCTCCT[C/T]GTCTGCTTACAATGA	84132
rs536304456	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104684	CAGACGCGCGACCAG[C/T]CCAGCCAATCAGCGC	84132
rs536352000	snp	C/T	1.96524e-05	0.00313461	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111200	AATCAGCCTGGCAGC[C/T]CCGAGGCAGTCTCAC	84132
rs536362963	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6110071	ACTCCTGACCTCAAG[C/T]GATCTGCCCACCTTG	84132
rs536374782	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094332	GCATGCACCAGCACC[C/T]GGCTAATTTTTTATT	84132
rs536379680	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6142495	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC	84132
rs536406131	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6132936	TTGGTCTCCCAAAGT[C/G]CTGGGATTACAGGCG	84132
rs536417930	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121717	TTGCCCAGGCTGGAG[C/T]ACAGTGGCAAGATCA	84132
rs536432649	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080049	CAACATGGTGAAACC[C/T]CGTCTCTACTAAATG	84132
rs536485647	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6099638	CAGGTGTGAGCCACC[A/G]CACCTGCCCCAATTT	84132
rs536487611	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6160134	TTTTTCCCTTGAAAG[A/G]AAACTTTGTCCAAAT	84132
rs536513775	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160339	GGAGGCATCTGGGGC[A/G]GGTGGTGGCCGGGCC	84132
rs536595884	snp	A/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6125895	TTGTGGTAACTAGAT[A/T]CACATGCACTTGTAA	84132
rs536611190	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6110123	ATAGGCATGAGCCAC[C/T]GCGCCCGGCCTCCTG	84132
rs536629123	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091891	AGCACTCTCAATCGG[C/T]ATTTCTTCCTGAAAT	84132
rs536636997	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6155741	TCAACTTGAAATCCA[A/G]TTGGGAAATTTGCTT	84132
rs536640376	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6085026	ACCCAGCCAAGGACT[C/T]TTAAGTGTAACTGAT	84132
rs536651953	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6129009	TAGAGACAGGGTTTC[A/G]CCATGTTGCCCAGGC	84132
rs536696218	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6108561	TCTCAGCTCACTGCA[A/G]CCTCCACCTCCCGGG	84132
rs536705742	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097230	CTGTCTCTGCCCTCC[A/G]TGGTCCTGGTAAAAC	84132
rs536733319	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6110920	TTTTAAAATAAAGAT[A/T]GTTGACATTCAGATT	84132
rs536766031	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104250	ACCACGCCCGGCTAA[A/T]TTTTTGTATCTTTAG	84132
rs536910099	snp	A/T	0	0	intron-variant	USP42	GRCh38.p7	7:6085923	CAGCCTATTAGTCTA[A/T]ATTTTTTATAAATGC	84132
rs536914421	snp	C/T	0.0158469	0.0875917	intron-variant	USP42	GRCh38.p7	7:6092152	TTCTTCCTCTTCCTC[C/T]TCTTCTTCTTCTTTC	84132
rs536923490	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156452	ATTACAGTGAAGGCA[A/G]ACTTGTTAAATTTTT	84132
rs536945010	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114839	AGGACTACAGGTGCC[C/T]GTCACCGCGCCTGGC	84132
rs536971321	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086447	CCTGACATCATGATC[C/T]GCCCACCTCGGCCTC	84132
rs536972755	snp	A/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077154	CTGGGATTACAGGCG[A/T]GATGAGCCACCGTGC	84132
rs537010801	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6085317	TTTTTAGTAGAGATG[A/G]GGTTTCACCACTTTG	84132
rs537023132	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6120126	CCTGCCACCACGCCG[C/G]CTAATTTTTTTGTAT	84132
rs537041366	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6078471	GCCGGGCATGGTGGC[A/G]GGTGCCTGTAGTCCC	84132
rs537058350	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145387	ATGCATTAGGTTTTT[C/G]CTAGAATATCACAGG	84132
rs537060334	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077699	AACTCCGTCTGTACT[A/G]AAAATGCAATTTTTT	84132
rs537067425	in-del	-/C	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6129706	TCTCTACTAAAAATA[-/C]AAAAATTAGCCAGGT	84132
rs537075958	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155382	TAAAAATTTGCCCTG[C/T]TTTGAAGCTGTATCT	84132
rs537078878	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6108163	TTGCATTCCAGCCTG[G/T]GTGGCAGAGCTAGAC	84132
rs537102434	snp	C/T	0.000399281	0.0141238	synonymous-codon	USP42	GRCh38.p7	7:6154785	GGACTGGAAGCCCTT[C/T]CACGGCGGCCGCGAG	84132
rs537119107	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159211	CTGTTCTAACATCAG[A/G]CTGCGTGTGGGTTGG	84132
rs537137952	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124617	CTTGCTTTTTATCCA[A/G]TAGTAGCCTCTGCCT	84132
rs537143839	in-del	-/TA			intron-variant	USP42	GRCh38.p7	7:6132321	TTTTACCTTTGTTCC[-/TA]TATATACATAATGAT	84132
rs537191872	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130101	AGCAGTCCTCTTGCG[G/T]CGACCTCCGAAAGTG	84132
rs537226534	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096270	TTGAGGCCAGCAGTT[C/T]GAGACCAGCTTATTA	84132
rs537238034	snp	C/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6147430	GCCTGGGCGACGCAG[C/T]AAGACCCTGTCTCAA	84132
rs537243331	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6141793	TTACAGATGTAATAC[A/G]TGCTTATGATAAAAA	84132
rs537248622	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146902	CTCTGAGCACCTGGC[C/G]TGGTCACAGCCAGCA	84132
rs537266504	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141269	ATGCAGTGGCGTGAT[A/C]TCGGCTCACTGCAAC	84132
rs537405869	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133479	TCTGTGGTGTCTAAT[C/T]TGTTATTAATTACAT	84132
rs537430796	snp	A/G	0.000538721	0.0164034	intron-variant	USP42	GRCh38.p7	7:6157131	AAAGGTGATTAACAT[A/G]TAGAAAGAAAACCTC	84132
rs537447326	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145801	TTGGCCGGGCGCAGT[A/G]GCTTACTCCTGTAAT	84132
rs537476277	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113720	TCCGCCTCCCGGGTT[C/T]ACACCATTCTCCTGC	84132
rs537499878	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100091	CTCCTGGCCTCAAGC[A/G]ATCTTCCGGCCTCAG	84132
rs537535951	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6088350	AACCTCTGCCTCCCA[C/G]GTTCAAGAGATTCTC	84132
rs537537883	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119738	TGACATTCTTGCTCT[C/G]TTGCCCAGGCTAGAG	84132
rs537539516	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6113296	GAAACACAACCTAAT[C/T]GAATGTTGCACATGG	84132
rs537550221	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119246	AACCAGGTAAGTCCT[C/T]CAACTTTGTTCTTTC	84132
rs537568727	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6112824	CCAGTGTGGCCCAGG[A/G]AAGCCAAAAGATTGG	84132
rs537580375	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138443	TTTAAAATCACCAGC[A/G]TAGCATTTTGGACAA	84132
rs537586814	in-del	-/ATTT			intron-variant	USP42	GRCh38.p7	7:6083270	TTTATTTATTTATTT[-/ATTT]TAGATACAGTCTAGC	84132
rs537603102	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6129529	GCTACTGCACTCCAG[A/G]CTGGGTGACAAAGTG	84132
rs537643979	snp	A/G	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6154532	GCGACCGCCAGGACC[A/G]CCACGCCCCGGAGCA	84132
rs537662136	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6134468	TTTATTGCAAGACAG[A/G]GTTAATTGGGAATAG	84132
rs537698324	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6099904	GGAGGTGGAGGTTGC[A/G]GTTAGCCAAGATCAC	84132
rs537703004	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6102555	CCCTTGAGGCCAGGG[A/G]TTCACAACCAACCTG	84132
rs537705348	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6134030	GAGTAGCTGGGACTA[-/C]CAGGTGCCCACCACC	84132
rs537755339	in-del	-/ATTTATTTATTT			intron-variant	USP42	GRCh38.p7	7:6083262	TTTATTTATTTATTT[-/ATTTATTTATTT]TAGATACAGTCTAGC	84132
rs537766135	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108584	CTCCCGGGTTCAAGC[A/G]ATTCTCCTACCTCAG	84132
rs537782559	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140550	TTTGTGTTTTGTTGT[A/T]GTTCATGGAGCATCC	84132
rs537798148	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133814	CGTAAGCCACCGCAC[C/G]TGGTGCATTTTTCAT	84132
rs537819956	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094233	GGCTGGAGTGCCATC[A/G]TGCCATAATAGCTCA	84132
rs537836710	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080624	GACAATCGCTTGAAC[A/C]CGGGAGGTGCAGATT	84132
rs537889548	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081452	AGAACTCGTCCGCCG[C/G]ACAGCCAATCGCGCC	84132
rs537898039	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087117	GCCCACTGCAACCTC[A/T]GCCTCCCATGTTCAA	84132
rs537907766	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092828	AGATTAAATATATCC[C/T]TCCTTGAACACTTTC	84132
rs537918421	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6160812	AATAGAACATCTCAA[A/T]TGCTGCTTAATTACA	84132
rs537967698	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098866	TGCATTGTCTTGTAG[A/G]GTACCTACCTCATTT	84132
rs537969558	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6092345	CACCACACCCAGCTA[A/G]TTTTTGTATTTTTAG	84132
rs537978638	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144887	AAAAAAAAAAATTAT[G/T]TTCAGAGTTGTCATT	84132
rs538027239	snp	C/G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125880	AACTCAACTTTTTAT[C/G/T]TGTGGTAACTAGATT	84132
rs538052147	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6144513	CCACTTTCTGAAGAT[C/T]GAAAGTGGTCAAAAA	84132
rs538096310	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6094831	TTTTTTTGGTCACCC[A/G]GGCTGGAGTACAGTG	84132
rs538102282	snp	G/T	0.00676609	0.0577691	intron-variant	USP42	GRCh38.p7	7:6122286	ATGTGTCAGTTTTTT[G/T]TTTTTTTTTTTTAAA	84132
rs538210511	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127301	AATTTTGGTGAAGTT[C/T]AATTGGTCAGCCTTT	84132
rs538234074	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157661	ATAGAAATACTTTTG[C/T]AGCGTATACGTTACT	84132
rs538253603	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147966	CTCTCAAGTTGAATT[A/G]TAGTGGTTGCTGTGT	84132
rs538263245	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6152677	GCCAGGTAGCGTGAG[C/G]GTGAGGTAGGTGGCT	84132
rs538268480	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161433	AATAATCTGTATGGT[C/T]TATACAGTTTGTGTT	84132
rs538291205	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6100432	CCTCCTGGGTTCAAG[C/T]GATTCTCTTGCCTCA	84132
rs538299886	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6156698	GCCAAGCTCCAGGGT[C/T]TGCTGCTGGTGGTTT	84132
rs538352617	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136212	TTTCTCCATGTTGGT[C/T]AGGCTGGTCTCAAAC	84132
rs538391494	snp	G/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6132425	TGCAGTGTTGCGATC[G/T]CAGCTCACTGCAACC	84132
rs538422850	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6158943	CTGTGGTCAGGCGTT[G/T]TCTGTGTGGTGGCCC	84132
rs538477594	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098283	CCTTGACAAAGTGTG[A/G]GATCTGTATTAAAGG	84132
rs538498891	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136712	AAGTTAATTAGGCTA[C/T]TCTGGACACACTGCC	84132
rs538504666	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081093	ATACCATTATTTGCT[C/T]TGATCCTTTAGTTTA	84132
rs538525248	in-del	-/T	0.49681	0.0398085	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079786	TACAAAACGTCATTC[-/T]TTTTTTTTTTTTTTG	84132
rs538560242	in-del	-/CTTTTCCT	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6086716	TTTCCTTTCCTTTTC[-/CTTTTCCT]TTTTCCTTTCCTTTC	84132
rs538562724	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6111046	AATGGCTGGAATGAT[C/T]TTCCAAGATCTAACG	84132
rs538606211	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116259	TGTCACTGCCCGCAA[C/G]CTCCTGGAATTCAGA	84132
rs538611746	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6119963	TGCCTCAGCCTTTTT[C/T]TGTTTTTGTTTTTGT	84132
rs538656694	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6118499	TTTATTCCAGTCTGG[C/G]TGACAGTAAGACCAT	84132
rs538659858	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110312	GCTTCATTTTATAGG[C/T]CCTGGGGATTCTGTC	84132
rs538672662	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6141710	ACTACAGCGACTGTG[C/T]CCAGCCTGCCTCTTG	84132
rs538691096	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104225	GTAGCTGGGACTACA[A/G]GCGCGCGCCACCACG	84132
rs538717420	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6121626	GCCATCTGGACCTTG[C/T]AGTTTCTCATGGGCA	84132
rs538732045	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6115911	GGAGACCAACCTGGA[C/T]AACATAGTAAGACCC	84132
rs538747138	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121202	ATAGAGGTGATAAGA[C/G]TAAAAATCCATGTCT	84132
rs538752244	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114800	GGTTCACGCCATTCT[A/C]CTGTCTTAGCCTCCC	84132
rs538785049	snp	A/G	0.00517822	0.0506191	intron-variant	USP42	GRCh38.p7	7:6141406	GATGGGGTTTCACCT[A/G]TCGGCCAGGATGGTC	84132
rs538792878	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6146859	GCCAGGAGCCACAGG[A/G]CAATGAGTGGAGACC	84132
rs538799927	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131919	ATATTCTCATGGGGT[A/G]TAGAATTCTATGTTA	84132
rs538799992	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137497	CCAAGTAGCTGGGAT[G/T]ACAGACGTGTACCAC	84132
rs538828171	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125801	TGTTTATTTTACTTT[C/G]TTGTTGATTTTAGTT	84132
rs538844820	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6085893	GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC	84132
rs538847262	in-del	-/T	0.386313	0.209568	intron-variant	USP42	GRCh38.p7	7:6122280	TATGTCATGTGTCAG[-/T]TTTTTTTTTTTTTTT	84132
rs538892894	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159925	CTGCTGTCTGCGCCC[C/T]GAGGTGGCACTGAGC	84132
rs538928124	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133319	CTTCAGACTCTAATG[A/G]TGTATATCAGGGGCA	84132
rs539107131	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095516	CTACTAAAAATACAA[A/C]AAATTAGCTGGGCGT	84132
rs539129436	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103625	GCTGCATCAGGTCTT[C/G]GGCGGTGGCTCCGGA	84132
rs539130524	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109092	AGGGGTTTCTAACCC[C/T]GTCTTGGGGGAATGG	84132
rs539170977	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6145363	GCTAAATGCACTAGG[-/T]TTTTTTAAATGCATT	84132
rs539233252	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6151837	GGGTTTGTTTACACC[A/G]GCATCACCACACTCA	84132
rs539278048	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6091251	CTTTTTTGAGGCAGG[G/T]TCTTGCTCTGTTGCC	84132
rs539282528	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091815	AGCTATTTTGCCCCA[A/G]CTGGGCTTGATCCCT	84132
rs539324140	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084271	ACCTCAGGAGATCTG[C/T]CCACCTTGGCCTCCC	84132
rs539400448	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083769	TTGTTTTAGGAACTC[A/T]CCATCTTAGGGCATG	84132
rs539430979	snp	C/T	8.64715e-05	0.00657482	missense	USP42	GRCh38.p7	7:6154976	GAACTGCACTTGTAG[C/T]CGGAGACAACTGTAA	84132
rs539434571	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6129449	GTAATCCCAGCTATT[C/T]GGGAGGCTGAGGAAG	84132
rs539444180	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077120	TCTTGTGATCTGCCC[A/C]CCTCAGCCTCCCAAA	84132
rs539456631	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6082368	CTCCTGACCTCGTGA[C/T]CCGCCTGCCTTGGCC	84132
rs539467163	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158770	TTGGTACCCGAGGAT[C/G]CGAGGATGCAGTGGA	84132
rs539467733	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6125629	TAAATTCATTTTAAA[A/G]GTTTTGTTTTAGATA	84132
rs539469582	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089619	CTCACTGCAACCTTC[A/G]CCTCCCGGGTTCAAA	84132
rs539499374	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158339	GGTTTGTCACCCCTG[C/T]CTGGACGCCCATTGT	84132
rs539509271	in-del	-/C	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6159622	AGAGCCATGGAGAGG[-/C]CCCGGCAGGTTCCCA	84132
rs539515030	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120879	GTGAGCCACTGCACC[C/T]GGCTGGAATAAATAT	84132
rs539518003	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081745	GACTGCGCCTACGTG[C/G]ACTGCGGGTTCGCTC	84132
rs539547876	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6134359	TTTCTGCATCTTTGC[A/G]TGCCTTGTACTGTTT	84132
rs539586552	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114359	TAAATGTTCAAAGTG[G/T]ATATAAAAGAGTAAT	84132
rs539605803	snp	C/G	0.00755907	0.0610114	intron-variant	USP42	GRCh38.p7	7:6133930	GCGTCTTGCTCTGTC[C/G]CCCAGGCTGGAGTGC	84132
rs539609780	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6113035	CAGCCTCCCGAGTAG[C/G]TGGGACTACAGGTGC	84132
rs539651504	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	USP42	GRCh38.p7	7:6078265	TACATTGCAATAATT[A/T]ATACATGTTAAACTC	84132
rs539663328	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126087	TGTCCCTGCCTTCCC[C/T]TTAACCTCTGGTGAC	84132
rs539679751	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108520	AGAGTCTCGCTCTGT[C/T]GCCAGGCTGGAGTGC	84132
rs539684771	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6084997	GTGCTGCGATTACAG[C/G]TGCGAGCCACCGCAC	84132
rs539715421	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077927	CTGCTGACCTCATGA[C/T]CCACCCACCTCAGCC	84132
rs539833267	snp	C/T	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6154472	AGAGCAGGAGCAAGA[C/T]TGAGGGCCACCGTCA	84132
rs539844064	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137746	GTGCAGTGGTGCAGT[C/T]TTGGCTCACTGCAAC	84132
rs539879642	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6092496	AAGGACCTATTTCAA[A/G]TGCCATTTCTGTTGT	84132
rs539883555	in-del	-/CAAAAAAAAAAAAAAAAAAAAAAAAAAGAA			intron-variant	USP42	GRCh38.p7	7:6135651	AGTGAGACTCCATCT[lengthTooLong]CAAAAAAAAGTAAAT	84132
rs539920926	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123506	GTCTCTACTAAAAAT[A/G]CAAATATTAGCCAGG	84132
rs539923897	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6158180	CCTCAGTGTCTGTGG[C/T]TTGATTGGGGCGCAG	84132
rs539974158	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137083	TGCAGTAAACTTTTG[C/T]ATCTTGTTAATTGAG	84132
rs539978776	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114899	GTTTCACCTTGTTAG[C/G]CAGGATGGTCTCGAT	84132
rs539983138	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6123286	CCCAACACTTTGGGA[A/G]GCTGAGGCAGGAGGA	84132
rs540005035	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6097312	TAGCATGTCCTCTTC[C/T]CTGAGAGTAGCACTC	84132
rs540008532	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117555	TTTCTCTTAGGTAAA[G/T]ATCTAGGAGTAAAAT	84132
rs540013175	snp	C/T			missense	USP42	GRCh38.p7	7:6154868	GTAGGGGCTGCGAGC[C/T]GGCCCGGGAGAGGGA	84132
rs540017149	in-del	-/A	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6159857	GTCCCCAGCACAGGC[-/A]ACCTCACTCAGGAGA	84132
rs540021112	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081364	GGGGCCGGGCCGCCG[C/T]GGGGAGGTAGATGGC	84132
rs540028171	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140479	GGCCTAACAGCCTTC[G/T]ACAGTTGGAGTAGTG	84132
rs540061122	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6139726	TCCCTGCCCTGGCAC[C/T]GCCCTGTCTAGGACT	84132
rs540065731	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157711	GTAGCATTCTGAGTG[C/T]ACCCTGATGCTCGGT	84132
rs540080958	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080804	AGTATAGCATGGTAG[C/T]CCATAACTGGATTCT	84132
rs540081592	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6153572	ACACCAGCATGGCAC[A/T]CGTATACATATGTAA	84132
rs540137631	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime	USP42	GRCh38.p7	7:6160989	CTCTCACCTAGACTT[C/T]GGAGAGCAGTCTGTT	84132
rs540143620	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6138316	AAACAGGACTGAAAT[A/G]TTTCTGTGCACCTGC	84132
rs540160667	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151824	CTGGCAGTGCAGTGG[A/G]TTTGTTTACACCAGC	84132
rs540183847	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6117324	TCATATTATCTCGCT[G/T]CTTTCACTCAGCATA	84132
rs540194794	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6126563	GTGCTGGGATTACAG[C/G]CATGAGCCACTGTGC	84132
rs540339896	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105857	GCAGTGGAGATGACT[G/T]TTGTTAATGACTCTT	84132
rs540356017	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6125437	GGGGGTTGCAGTGAG[C/T]CAAGAACACACCACT	84132
rs540382144	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6122800	ATAGAGATAGGGTCT[C/T]ACTAAGTTGCTCAGG	84132
rs540425464	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143249	GACATTATTGGGCAG[A/G]TTCGGTGGGAGGAGA	84132
rs540439547	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142849	TGATTGTGCCACTGC[A/G]CTCCAGCCTGGGTGG	84132
rs540449889	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122371	GCTCACTGCACCCTC[A/C]ACCTTCTGGGTTCAA	84132
rs540523968	snp	A/C	3.46344e-05	0.00416125	intron-variant	USP42	GRCh38.p7	7:6141014	TATGGGAGTAATTAC[A/C]TTTTTAAAATAAGTC	84132
rs540536066	snp	A/G			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161743	TGTTTGCTGGACCCA[A/G]CAATATCTGTTTTAA	84132
rs540544844	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093116	AGTAAACGGAAGGTA[C/G]TCTTTCTTCCTTCCT	84132
rs540549031	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126881	ATTTCTCTGGGATAA[A/G]TGCCCAGGACTGCAA	84132
rs540549608	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110591	TTAAAGGTGAGATCT[C/G]TATAATTATAATTTT	84132
rs540597411	snp	A/G	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6109200	GTTGGAAAAGAGTCG[A/G]AGAAAAGAACAGCAT	84132
rs540610531	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116058	GCAGTGAGCTGTGAT[C/T]GCACTGCTGTACTTC	84132
rs540615177	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079703	ACCCTCAAATCCTCA[C/T]CCCCTAATGGTAGAT	84132
rs540655553	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156528	AGTCGTAGCTCACTG[C/T]AGCCTCAATCTCCTG	84132
rs540675689	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6079327	GCCCGGCGGGGTGGC[A/G]CGTGCCTGTAATCCC	84132
rs540687075	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6155988	TCTCAAACCCCTAGA[C/G]TCAAGCGATCCCAAA	84132
rs540706701	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6085491	TTCCTCCTAGTGTTG[C/T]ACATAATTAGTGAGT	84132
rs540730573	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159769	CCCTTGTGCCTCACT[G/T]GGGAAAAGCCAACCC	84132
rs540747339	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131535	AAATACACACAGAAG[A/C]TGAAGTAGAGCAATG	84132
rs540786395	snp	A/G/T	8.62466e-05	0.00656635	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111309	TAGGACCAGTACCTG[A/G/T]TGCTGTAGTTTATTC	84132
rs540800034	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6105543	CGGCCTCCCCGCCCC[C/T]ACTGCATCCCTAACA	84132
rs540807296	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6120261	GAGCCACTGCGCCCG[G/T]CCCTTTTTATTTGCT	84132
rs540815130	in-del	-/A	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6131473	GTGAGATGCTGTCTC[-/A]AAAAAAAACAAACCA	84132
rs540833263	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148067	AAACGGCCGAGCGCA[A/G]TGGCTCAAGCTTGTA	84132
rs540858103	snp	A/G	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6130870	GAGCAAGGGGAAGGC[A/G]TTATTGGCCAGAGCC	84132
rs540860690	snp	G/T			intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153212	CAGGAGATGGAGGTT[G/T]CAGGGAGCTGAGATC	84132
rs540870634	snp	A/G/T	6.09686e-05	0.00552099	intron-variant	USP42	GRCh38.p7	7:6135968	TAAGTATTAACTATT[A/G/T]TAGTTTTATATTTGT	84132
rs540900686	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6116548	TATTAGTTACTAGGA[A/T]TTAAAAAAAAAAATC	84132
rs540924137	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104341	CCCGCCTCGGCCTCC[C/G]AGAATGCTGGGATTA	84132
rs540938193	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6109804	CTCCCAGGTTCAAGC[A/G]ATTTTCCTGACTCAG	84132
rs541000444	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6094716	GGCACTATTCTCTGC[A/G]ATTTTCTCCCATCAA	84132
rs541004338	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141510	CTGAATTTTCATTTA[A/C]TATCTTAATAAAACT	84132
rs541026404	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6145216	CGCACCTGTAATCCC[C/G]GCTACTCGGGAGGCT	84132
rs541054506	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134567	TCGGTGCTGCCAACA[C/G]TTTGGGTGACTCTTT	84132
rs541063569	snp	C/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6117404	TTGTTGAGTAGGATT[C/G]CATTTTATGGCTAGA	84132
rs541097595	snp	C/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114769	TATCTCAGCTCACTG[C/G]AAGCTCTGCCTCCCG	84132
rs541156790	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6111734	CAGCCTCCAGAGTAG[C/G]TGGGACTACAGGCGC	84132
rs541162189	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113956	AGCACTGGGGGACTG[C/T]CAAAGCCTTTGAAAA	84132
rs541187410	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130605	TTCTCCACCGTTAAC[C/T]CAGTATGGGTTAGGG	84132
rs541209889	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6078014	GGCACGGTGGCACAC[A/G]CCTGTAATCCCAGCT	84132
rs541273823	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083919	CCCTAACCTAGTTAA[A/C]CTCCTGCCCCTTTTT	84132
rs541285451	snp	A/G	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6135363	TTGTTAGAAAAGTAA[A/G]TGAGGCTGGGGTGGT	84132
rs541285831	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6083191	TGGCCTCCCAAAGGG[C/T]TGGGGTTACAGGCGT	84132
rs541291293	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158967	GTGGCCCTGTGTTTC[C/T]GTCCCCGTCCCACTG	84132
rs541295615	snp	C/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6141943	ATGTCTGTCTGGCCA[C/T]TCACTGTTCCGTGTA	84132
rs541316810	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096671	AAGTTGATTAATCCC[C/T]GGAGATTAATCCCAA	84132
rs541368864	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6121182	GACCTCCATTACATT[A/G]TTAAATAGAGGTGAT	84132
rs541417266	snp	C/G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6134107	TGTGTTAGCCAGGAT[C/G/T]GTCTCGATCTCCTGA	84132
rs541438978	snp	A/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6128432	ATGCCCAGATAAAAT[A/T]TTTTCCCTGCTTTGT	84132
rs541473376	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6102636	TGGGCTGTGCCTGTG[G/T]GGACACACTGTGGGC	84132
rs541474520	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6132605	CTCAAGTGATCTACC[C/T]GCCTCAGCCTCACAG	84132
rs541478594	snp	A/G	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6139970	TCTGGCCAGGAAGGG[A/G]TGCTCTTGGGCTGCC	84132
rs541517932	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143171	AAGGCGAGAGCCCGG[A/G]GTGTCTTGATGTGTG	84132
rs541547086	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6101170	AGAACAGCCTCAGGA[A/G]AAGAGGCAGCTGTGA	84132
rs541548974	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108286	CTCATGCCTGTAATT[C/T]CAGCATTTTGGGAGG	84132
rs541550738	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6119791	TCACTGCAGCCTTGA[C/T]CTCCTTGGCTCAAGG	84132
rs541637048	snp	A/G	5.44484e-05	0.0052174	synonymous-codon	USP42	GRCh38.p7	7:6139174	TGCTATGCAGAAAGC[A/G]TGCTTGAATGGCAGC	84132
rs541662807	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124298	TTTGAGACGGATTCT[C/T]GCTCTGTCACCCAGG	84132
rs541681838	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6118769	AAATTGTCTTTGCAC[A/C]TTTATCAAAAATCAG	84132
rs541776512	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129632	TTGGGAGGCCGAGGC[A/G]GGCGGATTACCTGAG	84132
rs541780151	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6130926	CAGGGTAGGGCAGGG[C/G]GAAGAATTTGGGATT	84132
rs541785410	snp	C/T	0.00557542	0.0525036	intron-variant	USP42	GRCh38.p7	7:6111858	GACCTCATGATCCAC[C/T]CACCTCAGCGTCCTG	84132
rs541825692	snp	A/C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6082101	TACGTGTATGTATGC[A/C/G]GAAAATATATATTTA	84132
rs541851858	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098398	ATTCCCGGGCTTATT[C/T]TCAGTTTCTGCTGGT	84132
rs541887077	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081433	CTTTGCGCTCGCGGG[C/T]CCCAGAACTCGTCCG	84132
rs541889845	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080711	GTCTCAAAAAAAAAA[A/C]AAAAAAGTACTCATA	84132
rs541890903	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6122587	GCGATTCTCCTGCCT[C/T]GGCCTCCTGAGTAGC	84132
rs541903352	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120836	TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	84132
rs541923219	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6093795	TTTATATATTTTCTT[C/T]TTTGTTTTTTTCATA	84132
rs541924407	snp	A/G	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6151314	ATTTCTTCAATAGTA[A/G]ACACACCTTAGCTTA	84132
rs541968842	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161828	ACAGTATCTGCAAGA[A/G]CTCTGACAGCCATCC	84132
rs541995778	snp	C/G	3.47572e-05	0.00416862	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116820	ATTCCCCACAGACAG[C/G]TTTCCTATCACTTTT	84132
rs542017883	snp	C/G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6107725	CTTCTTTCTTTTTTT[C/G/T]CTGCATTTTTTTCTT	84132
rs542018742	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132758	CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCACG	84132
rs542074223	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6076778	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	84132
rs542084483	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6113028	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	84132
rs542091029	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080175	TTGCAGTGAGCCAAG[A/G]TCGCGCCACTGCACT	84132
rs542093688	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6093220	CTTCCTTTCTTCCTT[C/T]CTCCCTCCCTCCCTC	84132
rs542106348	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106879	CCTGTAGGTTGTTGT[G/T]TTAATGCTCTTGTAA	84132
rs542116285	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6126131	TTTCTATGATTTTGT[A/C]ATTTCAACAGTGTTA	84132
rs542129234	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6106470	CATACCATATAAGAG[A/G]CTGGGAATTTTAAAG	84132
rs542157719	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099473	CCCGCCTCGGCCTCC[A/C]AAAGTGCTGGGATTA	84132
rs542221624	snp	G/T	0.000482865	0.0155306	intron-variant	USP42	GRCh38.p7	7:6144054	GTGTATATATTCGTC[G/T]TCTTATACTTTTGTT	84132
rs542281849	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153514	GGCGAGATGTATTTA[A/G]AGAGACGAAATAGCT	84132
rs542286278	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097812	AGCAAGGATGGTCTC[C/G]ATCTCCTGACCTCGT	84132
rs542295195	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148217	GTGGTGTGTGCTGTG[G/T]TCCCAGCTGCTCAGG	84132
rs542323441	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142770	CATGCCTGTGGTTTA[C/G]CTGCTCGGGAGGCTG	84132
rs542347605	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105069	GCCCGCCGCAGGCCG[C/G]CATGGGGCCCGCGCA	84132
rs542354176	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153120	TCTACTAAAAACACA[A/C]ATATCAGCTGGGCAT	84132
rs542383589	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6118728	GTTCTAGCACCATTT[G/T]TTGGAAACATAATCC	84132
rs542402557	snp	A/G	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6133128	TGGACAACTTTCAGT[A/G]ACTTTTGAAAACTTA	84132
rs542414644	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6138536	CACTCTGTAGCTACT[C/T]TCTAGACTCTCAGAA	84132
rs542420407	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6117245	ATCTGCTTTCCGTCA[C/T]TATAGATGAATTAGT	84132
rs542437793	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080202	CACTCCAGCCTGGGC[A/G]AGAGAGCGAGACTCC	84132
rs542441450	snp	A/C	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6079477	ATAAATAAATAAATA[A/C]ATAAATAAATAGTAC	84132
rs542452861	snp	C/T	0.00557542	0.0525036	intron-variant	USP42	GRCh38.p7	7:6086601	GTGATCCACCCCCCT[C/T]AACCTCCCAAAGTTC	84132
rs542500281	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6160512	AGCCCTACACGCCGC[C/T]GCCTGCCTCCAACTC	84132
rs542504998	snp	C/T	0.000184392	0.00960011	synonymous-codon	USP42	GRCh38.p7	7:6156922	GACTGTCGCCCAGTT[C/T]CGGAGAGCCCAGGGT	84132
rs542507817	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144579	CTGAATTATTAAAAT[C/T]AAATAATCGGCCGAG	84132
rs542526849	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091988	TATTTTTTCTTCTTC[C/T]TCTTCTTCTTCTTCT	84132
rs542599229	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137035	ATTTTAAATGGGTAA[A/G]TGCATGAAATTTTCT	84132
rs542625271	in-del	-/AA	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6152032	CCTGCCCCACAATTT[-/AA]AAAAAAAAAATCATG	84132
rs542700070	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6159661	AGACCCAGGCCACGC[A/G]CTTGGGGACAGACCT	84132
rs542708418	in-del	-/TA	0.0232847	0.105357	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114645	GTGTGTGTATATATG[-/TA]TGTGTGTGTGTATAT	84132
rs542739930	snp	A/G	0.000399281	0.0141238	intron-variant, missense	USP42	GRCh38.p7	7:6130292	TCAGCCTCCGTTGGC[A/G]CCCCAGGTGGGAATT	84132
rs542755599	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110478	CAAGTCCTTTCATAA[C/G]AGATATTTGTGTTTG	84132
rs542767511	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096624	GGAAGAACAGGTGCA[C/G]AGCAGGAGGCTGTGA	84132
rs542792766	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147569	CTGATCTGAGTGCCT[G/T]ACATTAGCCTGAAGG	84132
rs542846119	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152403	CGTGCCAGTGACACA[C/T]CCGTAGTTTTTACCC	84132
rs542854233	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147177	GATCAGAGGAGGCCT[C/T]AGGCCAAGTTGAGGG	84132
rs542857909	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126498	CACCGTGTTAGCCAG[G/T]ATGGTCTCTATCTCC	84132
rs542862947	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6135462	AGGCCAGCCTGGCTA[A/T]CATGGTGAAACCCCA	84132
rs542884952	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6152115	AATTTGTCATGCAGC[A/G]TCAGTGGCTTCACCT	84132
rs542919892	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6101860	GAGGTGGGCAGATCA[C/T]TTGAGGCCAGGAGTT	84132
rs542924045	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098357	GCCCTCACCCCTCAC[C/T]CCTTGATCTAGGCCC	84132
rs542930244	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160217	AGAGTCTGTGGATTA[A/G]TTGGCCGTTAATTAA	84132
rs542959080	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120511	GCCTCCCAAAGTGCT[G/T]GGATTACAGGCATGA	84132
rs542970015	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126139	ATTTTGTCATTTCAA[A/C]AGTGTTACGTGAATT	84132
rs542987158	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113916	ATGAGCCACTGTGCC[C/T]GACCCAATCTCAGCC	84132
rs543022243	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124833	TTGATATTTTTTTTC[A/C]TGGTGGTTACTTTAG	84132
rs543052604	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6102407	GTGAGCCACCACGCC[C/G]AGATTCTACTAAGAT	84132
rs543056832	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155533	ATTGGGAGTCTTTGA[C/G]CTTAGAATTGGTGTT	84132
rs543086831	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084753	AGACGGAGTCTCACT[C/T]TGTCACCCAGCCTGG	84132
rs543086836	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6091328	CTCCTGGTCTCAAGC[A/G]ATCCTCCCACCTCCG	84132
rs543094661	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6090548	GGTGAAACCCCATCT[A/C]TCCTAAAAATACAAA	84132
rs543098413	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6082491	GGTGTAGTGGCTCAC[A/G]CTTGTAATCTCAGCA	84132
rs543099538	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113612	TCAGCCTTTTGGTTT[C/T]TTTTGTTTTTGTTTT	84132
rs543114872	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083803	ATTCCTCTTTTTTTC[C/G]CCTTCCTTACTCAAT	84132
rs543115568	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6097480	TGCATGATCATAGCT[C/T]ACCGCAGCCTCCAAT	84132
rs543136377	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119915	CCATGTTGCCCAGGC[C/T]GGTCTTGAACTCCTA	84132
rs543161949	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6158915	TGATCTTGTTTGCCT[C/T]GTGTCTCGGGTGCTG	84132
rs543202595	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124212	CATGTTAGCATGATA[A/T]ATTTTTTCCATCTTT	84132
rs543206271	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6109889	TATTTTTAGTAGAGA[C/T]GAGGTTTCACTATGT	84132
rs543239860	snp	C/T			downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161438	TCTGTATGGTTTATA[C/T]AGTTTGTGTTGTTCA	84132
rs543277595	snp	A/C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144851	CTCCAGCCTGGGCAA[A/C/G]AGAGTCAGATTCTGT	84132
rs543279724	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6109053	CCGTAGAAATCAGCA[C/T]AGGGTGCTGTGGGGG	84132
rs543313704	snp	A/T	0.0170251	0.090679	intron-variant	USP42	GRCh38.p7	7:6108796	AATATTAAAAAAAAA[A/T]TTTTTTAAGGCCATT	84132
rs543319230	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146518	AATACGAAAAAATTA[A/G]CCAGGTGTGGTGTTG	84132
rs543330809	snp	C/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115046	CAAATGAAGTCTACA[C/G]TTTGCATTTGGTAGA	84132
rs543386283	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6146072	ATCTCAAAAAAAAAG[A/T]AAGAAATATTTCTCT	84132
rs543448105	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6139927	ACAGCTCTGCGTCTC[C/G]TCCCGCCACTCCCAG	84132
rs543468027	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077348	TGATGATTCATGTAC[A/G]GAGAATTGATGGTAT	84132
rs543484947	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6150933	CCTTCTGAGAAATGC[A/G]TCGTTTGGGGATGTG	84132
rs543513683	snp	A/G	0.000798403	0.0199641	missense	USP42	GRCh38.p7	7:6155003	GTAACCTCTCTGATC[A/G]GTTTCACGAACACGA	84132
rs543555675	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107028	ATTGTTTAGCTTCAA[C/G]AAAGGTTATGTGTGT	84132
rs543628184	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095938	TTTTTTTTTTAATTT[A/G]TTTTTTTGTAGAGAC	84132
rs543632406	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148965	GCTTTCCAGTGTTAG[A/G]ATGGCAGCTAATTCA	84132
rs543652099	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089221	GGCTAATTTTTTTTT[C/T]TTTTGTATTTTTAGT	84132
rs543664566	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6095042	ATCTGCCCGTCTGGG[C/T]CTCCCAAAGTGCTGG	84132
rs543664663	snp	A/C	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6088737	TTCTCTTTCCACCAA[A/C]TCATCAAGGTGAGTT	84132
rs543691745	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103025	GGGTTAGATCACCAG[G/T]GGAGGGAAAGAGGCA	84132
rs543697404	in-del	-/TG	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6082026	CTGCGGGGACTTGTC[-/TG]TATTACATATATATG	84132
rs543776164	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101564	ATCATCTCAGCCAAG[A/G]CCCCAGCTGTTTGTA	84132
rs543809457	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6111562	GACAACAGGGTAGAT[A/T]GTTTTTAGTTGCTAG	84132
rs543825336	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122472	TTTGTTTTTTTGTTT[G/T]TTTGTTTGTTTGTTT	84132
rs543828637	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101071	GGGGAGCGCTCTAGG[G/T]AGGAAGGTAATGAAA	84132
rs543835780	in-del	-/AAAA			intron-variant	USP42	GRCh38.p7	7:6095674	CTCCGTCTAAAAAAC[-/AAAA]AAAAAAAATGGCCAG	84132
rs543868924	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145021	GATTCCGCTATCCTC[C/G]CGGTTAACCATGCCC	84132
rs543879723	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6130435	CCTCTGACCCTCACC[A/G]GGGGCTGGGGAGGCC	84132
rs543888891	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126989	TGCATCTTTGCCAAC[A/T]TTTGCTGTTGTCACT	84132
rs543892134	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128456	GCTTTGTTTTGATTA[A/G]TGCTTGCATGACATA	84132
rs543916463	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6157497	CTGCCTCCCAGGTTC[A/G]TGCTGTTCTCCTGCC	84132
rs543935819	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132730	AGGCTGGAGTGCAGC[A/G]TCGAGATCTCGGCTC	84132
rs543942710	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112985	CTCGGCTCACTGCAA[C/T]CTCTGCCTGCTGGGT	84132
rs544070013	snp	A/G/T	5.38073e-05	0.00518659	missense	USP42	GRCh38.p7	7:6153989	AGGACATCGTGGGGG[A/G/T]CACAGCACCCCCTGA	84132
rs544161894	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128597	TGTCTTTTAACTCTC[C/T]GCTGCTCTAGGCTGG	84132
rs544170610	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116714	CCAAAGAAAAATCAC[C/T]TAGAATCTCACCACC	84132
rs544236413	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119271	TCTTTCTCCGAGTTA[C/T]GCTGTAGCCTGGGCA	84132
rs544242824	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161767	GTTTTAAAGAACCAA[A/G]TCTTAGGCTTGTTTT	84132
rs544265841	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6139921	GCTCCCACAGCTCTG[C/T]GTCTCCTCCCGCCAC	84132
rs544265977	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093650	CTCCTTTCCTTACCT[C/G]TTTCTTCCTTTCTCT	84132
rs544278122	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6137824	TAGCTGGGACTACAG[C/G]TGCTTGCCACTACCC	84132
rs544278374	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093170	CCCTCCCTTCCCTTC[C/T]TTCCCTCCCTCTCTC	84132
rs544309817	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6156666	ACAGTGAATGTTCTC[A/G]GTGAATGGGTGGAAA	84132
rs544392951	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6112511	CATTTGTTATAATGA[C/T]ACAAATGTGGTTACA	84132
rs544396650	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6137794	CAGCGATTTCTCCTG[C/T]GTCAGCCTCCTGAGT	84132
rs544401770	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086103	TGCAATGCCAAGATC[G/T]TGGCTCATTGCAACC	84132
rs544444779	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6124338	AGTGGCGCGATCTCG[A/G]CTCACTGCAACCTTC	84132
rs544460342	snp	C/T	0.0170251	0.090679	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081379	CGGGGAGGTAGATGG[C/T]GGGCGGCGCAGCCAC	84132
rs544480533	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6098133	TGGTCTTGATCTTCT[C/G]AACTCGTGATCCTTC	84132
rs544499839	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6111764	CCTGCCACCAAGCCC[A/G]GCTAATTTTTTTTTT	84132
rs544502977	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157727	ACCCTGATGCTCGGT[A/C]CTGATTTGCTCGCTT	84132
rs544503734	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118303	GAGGCGGGTGGCTCA[C/G]TTGAGTTCAGTAGTT	84132
rs544547724	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143305	TGGTAGTGCTGCTTC[A/T]GGTGTGGCTGGGCAC	84132
rs544586564	snp	C/G	2.05227e-05	0.00320327	intron-variant	USP42	GRCh38.p7	7:6111391	TACTGTTTTTCAAAA[C/G]AGAGAATTACCGCCA	84132
rs544648644	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	USP42	GRCh38.p7	7:6153041	TTTGGGAGGCTGAGG[C/T]GGGCGGATCACCTGA	84132
rs544652431	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086556	GTTTTCACCATGTTG[G/T]CCATGCTGGTTTCAA	84132
rs544685491	snp	A/G	1.6947e-05	0.00291088	synonymous-codon	USP42	GRCh38.p7	7:6156847	GAAGAGACATTCAAG[A/G]AAATCAGAGGACTTT	84132
rs544685815	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152522	GTGGGAGTGCCCTCA[A/C]TGAGGCCCTCTGTTA	84132
rs544695821	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6091433	GGGTCTCCCTATGTT[A/G]CCCAGGCTGGTCTTG	84132
rs544819482	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106368	ATATTATTACCTCAA[G/T]GTATGCAGAGTGCCA	84132
rs544845421	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091975	GTCCTCAAGGACGTA[C/T]TTTTTCTTCTTCTTC	84132
rs544855759	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6130969	TAATTTTTGTGGGCT[C/G]TGAGCCACAGGTGTG	84132
rs544857881	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6097752	GCCGCCACCATGCCC[C/T]GCTAATTTTTTGCAT	84132
rs544860221	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148502	TCTTTAATTCCTGTC[C/G]GATTGCAGGAAAGCG	84132
rs544893779	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131581	TGTCACACGAGGCTG[C/T]CCCTTCCTCATCCTT	84132
rs544917457	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160090	GTTTTATACCTGACC[C/G]TTGTGGAGCTAGAGG	84132
rs544918627	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6097382	AATTAGGTCCCTGTG[A/G]GTCCTTTTTTTTTTT	84132
rs544985352	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142560	CATTTGCTGTTATAT[C/G]TTTGAGTCTTCTGTT	84132
rs545015417	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136030	TTTTTTTCGAGACAG[A/T]GTCTTGCTCTGTCGC	84132
rs545030967	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6142239	TTTTTTTTTTTGAGA[C/T]GGAGTCCTGCTCTGT	84132
rs545031719	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130154	CCGCGCCTGGCCATG[C/G]ATATTTTGGTGTTAT	84132
rs545136089	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134601	GGGAGGGGCTGTCCG[G/T]TGCATTCGAGGCTGT	84132
rs545226010	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155839	TCACTGCAGCCTTGA[C/T]CTCCTGGGCTCAAAT	84132
rs545244503	snp	C/T	0.0119091	0.0762411	upstream-variant-2KB	USP42	GRCh38.p7	7:6078598	CAGAGCAAGACTCCA[C/T]CTCAAAAAAAAAAAA	84132
rs545263948	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6152036	GCCCCACAATTTAAA[A/C]AAAAAATCATGTCAT	84132
rs545299704	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159390	ACGCACACACACAGC[A/G]GAGGCCCTGGCGATT	84132
rs545305604	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104881	CGCCCCCCGGCGGCC[C/T]GGAGGGGCGCGGCGG	84132
rs545325585	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6091796	GCAAAGTGGGGTGGT[A/G]TCTAGCTATTTTGCC	84132
rs545338055	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	USP42	GRCh38.p7	7:6084598	CACGCTGCGGCATCT[A/G]CTGTTGCATCTGCGA	84132
rs545342774	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6124407	CATGTAGCTGGGACT[A/G]CGGGTGCACCACCAC	84132
rs545353978	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136410	GTCTTTGATAACAAA[G/T]TTTTAGTAAAACATT	84132
rs545363744	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119387	GAGGTGAGAGGCTCG[C/G]TTCAGCTCAGGAGGT	84132
rs545419131	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089754	GTCAGGCTGTTCTCA[A/G]ACTCCTGACCTCGTG	84132
rs545422393	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6124807	ATTTAATCTGCTTCA[C/T]TGGCATATTTTTGAT	84132
rs545452339	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096581	TGGTTTAAACTAACA[A/C]GGTGACTGCATTCCA	84132
rs545471476	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6116534	GTATGTTCTGGGGCT[A/G]TTAGTTACTAGGATT	84132
rs545475146	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6118891	TGTTTGTCTTGACAC[C/T]GTAACACAATGTTTT	84132
rs545476970	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123617	GCAGTGAGCCGAGAT[A/C]GCGCCACTGCACTCC	84132
rs545482304	snp	C/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6150958	GATGTGGTTGTCATG[C/T]CAGCACCACAGTGTG	84132
rs545515228	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095904	AGTAACTGGGACCAC[A/T]GGTGCCACCATACTT	84132
rs545525782	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6102916	AACAGAGAAGAGACT[A/G]TTGAGATGGAATTGT	84132
rs545536933	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6089170	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	84132
rs545567172	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146665	GCAAGACTGTCTCAA[A/G]AAAAAACCAAAAACC	84132
rs545587228	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6120744	GCCCACCATCATGCC[C/T]GGCTAATTTTTGTAT	84132
rs545588834	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114426	ACATTTATCAACTTA[C/G]GGGCAGTGATACCAG	84132
rs545619319	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6132462	TCCCAGGTTCAAGTG[A/G]TTCTCCTGTCTCAGC	84132
rs545626808	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128984	CGCGACCATGCCTGG[C/T]TAATTTTTGTAGAGA	84132
rs545628515	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151662	TGGTCAGGCTGGTCT[C/G]AAACTCCTGACCTCA	84132
rs545639676	snp	C/G			synonymous-codon	USP42	GRCh38.p7	7:6154620	CAGTCACCACCACTC[C/G]CGACACCGGAGCGGG	84132
rs545649334	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108740	CGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA	84132
rs545690261	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146019	AGATTGCAAGATCAC[A/G]CCACTGCACTCCAGC	84132
rs545759945	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113864	CTGACCTTGTGATCC[A/G]CCCGCCTCGGCCTCC	84132
rs545815800	snp	A/C			upstream-variant-2KB	USP42	GRCh38.p7	7:6078190	AACCATTAAGCCACC[A/C]TGCTCTGATCCGTGA	84132
rs545871782	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6100743	GGCTGTAGTGCAGTG[A/G]TGCAAGCCCACCTCC	84132
rs545880737	snp	A/G	0.000372232	0.0136373	synonymous-codon	USP42	GRCh38.p7	7:6154329	CGGCGAGAGGGTCGA[A/G]GACGCCGCGGCGCCG	84132
rs545904086	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088649	TCACTACACCAGTGA[C/T]AGCGTCTCATCATCG	84132
rs545908246	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122772	ACTGTGTCCAGCCTA[A/G]TTTTTTTTTTAAATA	84132
rs546018888	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094504	ACTCCATTCTGTTGT[A/G]GATGTAGAAGAACTC	84132
rs546023521	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6112016	ATTCTAGTTTCCTAA[A/G]TAGATGACTTTTACA	84132
rs546085622	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113465	TTCTGGGGCTCTCAT[C/T]TCATTCTCCACAGAA	84132
rs546094547	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100352	ATGGTTTTTTAATAC[A/G]GAGTTTCGCTCTTGT	84132
rs546153232	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6107704	GTGAGCACCTGCGCC[C/T]GGCCTCTTCTTTCTT	84132
rs546167103	snp	C/T	0.00557542	0.0525036	intron-variant	USP42	GRCh38.p7	7:6091226	TTTCTCTTCTCTTCT[C/T]TTTTCTTTTCTTTTT	84132
rs546168795	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6108940	AGTTGTTCTCCACAT[C/G]TATGGAAAGCTTTCT	84132
rs546215515	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133255	CTCCTTTGTGCTTTT[C/T]GTTTGTAGATAATTG	84132
rs546216180	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6126316	TTGAGAGGAAGTCTT[A/G]CTCTGTTGTCCAGGC	84132
rs546216572	snp	A/G	1.68457e-05	0.00290216	synonymous-codon	USP42	GRCh38.p7	7:6140942	TTGCAAGGGCGTTTC[A/G]GATACTTTTGATCCA	84132
rs546219069	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138609	CCTAACCCCTGGGCC[A/G]TAGACTGGTACCCAA	84132
rs546229324	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6144608	AGTGTGGTGGCTCAC[A/G]CCCGTAATCCCAGCA	84132
rs546255931	snp	C/G	8.50449e-05	0.00652037	missense	USP42	GRCh38.p7	7:6150170	ACCCATGACCCTAAA[C/G]GGTGCTAATAGTGCA	84132
rs546267747	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156211	ATAGGCAGTGGTTAT[G/T]GGAGGGAAAAATAAT	84132
rs546269639	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160236	GCCGTTAATTAACAG[A/G]CTTTATCAATGTGTC	84132
rs546271997	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148794	GGCAGTATATTTGAG[A/G]TATAACAGAGTCACA	84132
rs546308346	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159903	CTCGTCCGTCCCGTC[C/T]CCTGTGCTGCTGTCT	84132
rs546329796	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6112973	CAGTGGCGCGATCTC[A/G]GCTCACTGCAATCTC	84132
rs546340806	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086762	ATGGAGTTTCGCTCT[C/T]GTCGCCCAGGCTGGA	84132
rs546362266	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118212	TAGCCTGGGCAACGT[A/G]GGGAGAACTCATCTC	84132
rs546385120	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6091772	TTGGAGACAGTGGGG[G/T]ATGGGGGTGCAAAGT	84132
rs546477022	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6122584	CAAGCGATTCTCCTG[C/G]CTCGGCCTCCTGAGT	84132
rs546480167	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6093743	TATGGTAGGTACTTC[G/T]TTTGAATGTATTTTG	84132
rs546515169	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6091972	TTAGTCCTCAAGGAC[A/G]TATTTTTTCTTCTTC	84132
rs546536624	snp	A/T	1.71079e-05	0.00292466	intron-variant	USP42	GRCh38.p7	7:6147922	GGAGAAGAACATTTT[A/T]ATGTTAATTTTTAAA	84132
rs546572214	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6111495	CTGAGTGGCCAGCAG[A/G]GTTGTATTACTTGAT	84132
rs546574401	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6147323	AAAAAATGAGCCAGG[C/T]GTGGTGGTGCATGTC	84132
rs546576349	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141680	TCCCCTGTCTCAGCC[A/T]CCCTAGTAGCTGGGA	84132
rs546578702	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6121533	GGGATATGTTTTCTT[C/T]GCATCTGTTTCCTGG	84132
rs546612341	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086354	GGGACTACAGGTGCC[C/T]GCCACCATGCCTGGC	84132
rs546622485	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6116254	TCTCTTGTCACTGCC[C/T]GCAACCTCCTGGAAT	84132
rs546633686	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6122006	TTTTTTAATGTTACT[G/T]ATCTTCTCAAAGAAC	84132
rs546634662	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6109430	GAGGCAGAGTCTCTC[C/T]ATGTCAGTCTGGAGT	84132
rs546637649	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146824	AGGGTGGGCTTCTGC[C/T]GCGGGCAGTAATGGA	84132
rs546640160	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121148	ATTAATTTTTCTTGC[C/T]GTTTTTTTCTAGTAA	84132
rs546640247	snp	C/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6126206	CTAGCATAATTCTCT[C/G]AAGATTGATCCAGGT	84132
rs546673897	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6133427	TATGGATATTTTCTA[C/T]CCATAATGAATATCT	84132
rs546676648	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6158621	TGCTGGGGAAACAGC[C/T]GGAGATGAGGACAGG	84132
rs546704128	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136672	GAATACTTTACTATA[C/T]GCAGTGACAGAAATT	84132
rs546710530	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6131700	TGGACTAGAAGAAGC[A/G]CAAAGAAACCCCAGG	84132
rs546719484	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120578	GTGTTGGGATTTCAG[A/G]CATGAGCCACTATGC	84132
rs546730084	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6156394	GGGACTGTTCAGGAT[A/G]GAGCTAAAGTTGGTG	84132
rs546781748	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155564	AATATTCTTACTTGT[C/T]AGATGTAGTTATGTT	84132
rs546791375	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6116971	CTACTGGTAGTTTTT[G/T]TGCTTGCTTCCTCCC	84132
rs546803136	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143375	GATAAGAGGGCTGCC[A/G]TCGGGTGGGGAGTCA	84132
rs546812626	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159728	GGGAAGACCCGCATC[C/T]TTCACGCAGGCAGAG	84132
rs546820144	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148295	TGAGCTGAGATTGCA[C/G]CACTGCACTCCAGCC	84132
rs546834192	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6120111	TTGGGACTACAGGTG[C/G]CTGCCACCACGCCGG	84132
rs546840634	in-del	-/TGG	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6098906	GCATAGTCTTCGGGT[-/TGG]TGGTACCATTCTTGA	84132
rs546862489	snp	C/T	0.000218203	0.0104429	intron-variant	USP42	GRCh38.p7	7:6143055	TGATGCCGGCTTCTC[C/T]AGTGGGGATGGCCGG	84132
rs546864208	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142367	GACTACAGGCGCGTG[C/T]CACTGTGCCCTGCTA	84132
rs546902757	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6138527	AACATGAGTCACTCT[A/G]TAGCTACTCTCTAGA	84132
rs546914722	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6121174	AGTAAAGAGACCTCC[A/T]TTACATTGTTAAATA	84132
rs546928415	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115181	TCTGTCTTTTAAAAT[G/T]TCCCTCTTCCCCCTG	84132
rs546959999	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103193	TTGGATGTGTGGATC[G/T]GGCACTCTGGAGCAA	84132
rs547072842	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6078914	CTGTCAATTAAGAGC[A/G]AATTGCCCTCATTTC	84132
rs547073456	snp	C/T	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6102338	AGGCTGGTCTCGAAC[C/T]CCTGATCTTGTGATC	84132
rs547093035	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151251	ACACTACTGTAGACT[C/G]TGGAAACACTGCACA	84132
rs547136103	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084889	ATGCCTGGCTAATGT[C/T]TACATTTTTAGTATA	84132
rs547136185	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	USP42	GRCh38.p7	7:6078255	GTTAATTTGTTACAT[C/T]GCAATAATTAATACA	84132
rs547136807	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108484	TTTTGTACTTTTACA[A/G]TATCCTTTTCTTTTA	84132
rs547181903	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120033	TGCAGTGGCGCTGTC[A/T]CGGCTCACTGCAACC	84132
rs547185231	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097507	CAATTCCTGGCCTCA[A/G]GTGATCCTCCCAGTT	84132
rs547193914	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124553	ACAGGAGTGAGCCCC[C/T]GTGCCCAGCTTTAAA	84132
rs547245806	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135616	AGGGTCACACCACTG[C/T]ACTCCAGCCTGGGTG	84132
rs547271730	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6119841	CATGAATAGCCAGGA[C/T]TACAGGCATGTGCTA	84132
rs547297913	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104641	GCCCAGGGAAGCACA[G/T]GGCGGAAGGAGCCCT	84132
rs547297961	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097095	ATGTTTAGTAGAGAC[A/G]GGCTGCTATCATCCT	84132
rs547315794	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109962	TGCCTCGGCCTCCCA[A/G]AATGCTGGGATTACA	84132
rs547339283	snp	C/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6095417	GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGCAG	84132
rs547340736	snp	A/C/T	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6129892	GGTTTCTTTTATATA[A/C/T]ATTTAGAACCATATC	84132
rs547343500	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6147121	TTGAAATATTAAACA[C/G]TGGCATTGGATTTCG	84132
rs547362024	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104118	CTCGCTCTGTCGCCC[A/C]GGCTGGAGGGCTGCA	84132
rs547373715	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6127127	TTGCCATCTGTTTGT[G/T]TTCTTTGGTGAAACG	84132
rs547374158	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089859	TTCTGATACTCATCC[C/T]TCAAGTGTCTGATGA	84132
rs547386727	snp	C/G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095981	TGCTCAGGTTGGTCT[C/G/T]GAATTCCTAGACTCA	84132
rs547420036	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081730	GCGCTGCTGAAAGCC[G/T]ACTGCGCCTACGTGG	84132
rs547425853	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6158254	CTGGCAGAGGTGAGT[A/G]GCTGCGGCAGGGCAG	84132
rs547427045	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6141142	TCAAGCTTTGTAGTA[A/G]GCATCATAAAAAAGC	84132
rs547475527	in-del	-/ATAT	0.00534426	0.0514156	intron-variant	USP42	GRCh38.p7	7:6090802	CATAATATATATAAC[-/ATAT]AGTTATATATATAGT	84132
rs547487969	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140442	CTCTTCGTATTAGCA[C/G]TCTTTTACATTTCAG	84132
rs547536272	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6106888	TGTTGTTTTAATGCT[C/T]TTGTAACTTTTATAT	84132
rs547543561	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108002	CCAGCCTGGCCAACA[C/T]AGTGAAACCCGGCTC	84132
rs547550460	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6157896	CACGCTGTGCTCTTA[C/T]TGCACTTGAGGCAGC	84132
rs547574748	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094725	CTCTGCGATTTTCTC[C/T]CATCAACCTCCACCC	84132
rs547607425	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6090759	TATATATTATATACT[A/G]TATATATTATATATA	84132
rs547626561	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6108308	TTTGGGAGGCAGAGG[A/C]AGGAGGATCGTTTGA	84132
rs547629565	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113625	TTTTTTTGTTTTTGT[G/T]TTTGTTTTTTTTTTG	84132
rs547631069	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	USP42	GRCh38.p7	7:6077454	GTGAGGAAGCCATGC[C/T]GTGAGTAGCCCTAGC	84132
rs547644141	snp	G/T	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6084262	GAACTCTTGACCTCA[G/T]GAGATCTGCCCACCT	84132
rs547675956	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089595	TGGAGTGCAAGGGTG[C/T]GATCTCGGCTCACTG	84132
rs547690551	snp	C/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6119684	CCTATTCATTTAGGC[C/T]TTGTTTTTTGTTGTT	84132
rs547705431	snp	C/T	0.0146672	0.084371	intron-variant	USP42	GRCh38.p7	7:6082277	GGGACTACAGGTGCC[C/T]GCCACCAGGCCCGGC	84132
rs547723082	snp	A/G	1.65674e-05	0.00287809	missense	USP42	GRCh38.p7	7:6150479	TCAGGCTTAGCAACA[A/G]ACTGAAAGGCTCGAC	84132
rs547878818	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6128025	ATCCTCAAAATCCTA[C/T]ATCATCAAAATTTTG	84132
rs547901257	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6085998	ACTGGCTGCCAACAT[C/T]GAGATGAGAGAAACC	84132
rs547939455	in-del	-/T	0.00199481	0.0315187	utr-variant-5-prime	USP42	GRCh38.p7	7:6084553	AGCTGAGTTAGCCAC[-/T]TAGGCACTCCACATC	84132
rs547971121	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6143778	AGTCTGAACATGTTC[A/G]TTTTTCAGTTTCTTT	84132
rs547986631	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6113147	TAATCCACCCGCCTC[A/G]GCCTCCCAGAGTGCT	84132
rs548032274	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144813	AGGCAGAGGTTGCAG[C/T]GAGCCGAGATTGTGC	84132
rs548071242	snp	C/T	9.54244e-05	0.00690674	missense	USP42	GRCh38.p7	7:6154429	CGCAGCCGGAGAGAG[C/T]GCTCGTCCAGCGGGG	84132
rs548093351	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144386	GAGAGCCTGTATAAT[C/T]TGAAATCCAAAGAGG	84132
rs548098103	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6119092	TGGGAACTCATGCCT[A/G]TAGTCCTAGTTACTT	84132
rs548152682	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106079	TTTGTCACTCATTCA[A/C]ATTGCCTAGGGGATA	84132
rs548161029	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6112161	GCTCTTTGAAAGAGA[G/T]CAGATAGGCTAGGCA	84132
rs548172904	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6099655	ACCTGCCCCAATTTT[C/G]CCTCTTTAAAGGATC	84132
rs548185740	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6117882	TCCGTATATTTCCTT[G/T]GCTAAAATGCCTGTT	84132
rs548192637	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6099150	TGCTGAGGAGGCTCT[A/G]CTCTCTGGCTTTCTC	84132
rs548231075	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6153703	TGTAATGCAATGACA[C/T]GAGCCTGTCAAGCCC	84132
rs548269043	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157572	CCGGCTAAATTTTGT[A/G]TTTTTAGTAGAGACG	84132
rs548296229	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122540	AGTAGTGTGATCTCG[A/G]CTCAACTGCAACCTG	84132
rs548299796	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096118	ATCTGGGCAGATGTT[C/T]GTGTTTTTCCACTGA	84132
rs548332369	snp	C/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6136690	AGTGACAGAAATTGT[C/G]AAAATAAAGTTAATT	84132
rs548334302	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6119543	AAATGAATTTTAGAA[A/T]CACTTTGTGAATTTC	84132
rs548339104	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100540	TCACCATGTTGGCCA[C/G]GCTTGTCTCGAACTC	84132
rs548343021	snp	C/T	5.03022e-05	0.00501484	intron-variant	USP42	GRCh38.p7	7:6142911	GCGGTGATGTGGTGT[C/T]TGTGCCTCTTCTCTT	84132
rs548343132	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133403	AGATTTTCTCTCTCT[C/G]TGTTTTATTATGGAT	84132
rs548368180	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127049	TGTAGTGGTAACTCA[A/G]TGTGGCTTTCATTTG	84132
rs548378737	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6126657	GTTTTGGGATATCGT[G/T]AGTGGAGCTGCGGTA	84132
rs548393939	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6099050	GTAGCTGAAAATTCA[A/G]CCTTTTCTAATGTTC	84132
rs548404282	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6138763	TGTGAACTGTGTGTG[C/T]ATGGGATCCAGGTTC	84132
rs548437795	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6132235	GGCCCGTTCTTTTTC[G/T]TTTAATACTTGAAAG	84132
rs548488471	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6107144	TTGGTTGGTTTTTCC[A/G]CAGTTACAATGCTGT	84132
rs548499700	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6101730	TGTAACCCCCCATCC[A/C]CTCCAACCTTAGAGC	84132
rs548538909	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137264	GGCATTATTGATAGA[C/G]CACAACAGACAAGCC	84132
rs548550734	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6106704	TAAGTAGGTAGGACT[A/G]CAGGCACATGCCACC	84132
rs548596501	snp	C/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6085081	GAACGACTGTGCCCA[C/G]CCTTGTTTTTGTGTT	84132
rs548603087	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143350	ATAGCATTTTCATTG[A/G]CTTTCTTATGATAAG	84132
rs548612373	snp	C/T	0.00874735	0.0655527	intron-variant	USP42	GRCh38.p7	7:6092176	TTCTTTCTTCTTCTT[C/T]TCTTTTTTTTTTTTT	84132
rs548662206	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159890	GGAGCCTTGCTCCCT[C/T]GTCCGTCCCGTCCCC	84132
rs548699046	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6087791	TGTTGTCCCATCTGC[C/G]TAGAAAGTCCCTCTG	84132
rs548713515	snp	A/G	1.65729e-05	0.00287857	missense	USP42	GRCh38.p7	7:6147845	GTCACCAACAAACAG[A/G]CTGCGCCAGGCTTTA	84132
rs548875227	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098716	CACCTGGCTAATTTT[C/T]GTATTTTTTAGTAGA	84132
rs548918924	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6115643	TAAGAAGTTGGTTTA[C/T]TCTTTTAGAAACCAA	84132
rs548961506	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6079373	TGAGGCAGGAGAATC[A/G]CTTGAACCCCGGAGG	84132
rs549000862	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125095	CTGAGGCAGGAGAAT[C/T]GCTTGATCCCGGGAG	84132
rs549005096	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6131076	GGATGGAGAAGGAAG[A/G]GCTCTGGATTGGTTA	84132
rs549031132	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6156177	ACCCTGGGAAAGATT[A/G]CCAAAAGCCATATGG	84132
rs549053390	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097484	TGATCATAGCTCACC[A/G]CAGCCTCCAATTCCT	84132
rs549061604	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6159556	GGGGACGCAGGCAGA[A/G]GAGTTTTAATTCTGC	84132
rs549114727	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116148	AGCAACTTGGGACAG[C/G]CGAGGTTAAGAAATC	84132
rs549153073	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6078173	AAAAAAAAATAAGCC[A/G]GAACCATTAAGCCAC	84132
rs549174068	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121460	CTATAGTTTCTTATA[A/C]TGCCTTTTTTTTTTC	84132
rs549194381	snp	C/T	0.000241672	0.0109899	missense	USP42	GRCh38.p7	7:6155111	GCGAACAGAAGGATC[C/T]TCTAGAAGAGCCTAA	84132
rs549200966	snp	A/C	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079924	CACCCCCCTACGCCC[A/C]CCAAAAAAAACTTCA	84132
rs549218026	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146772	CTGTGGCCATGAGCA[C/G]TGAAGGTGCAGCTGC	84132
rs549225762	snp	A/G	0	0	intron-variant	USP42	GRCh38.p7	7:6147431	CCTGGGCGACGCAGC[A/G]AGACCCTGTCTCAAA	84132
rs549232872	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159072	GCCGCTGCCCGGCCC[C/T]GCCTCACCCAGCGTC	84132
rs549238875	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124456	TTTTTAGTAGAGATG[A/G]GGTTTCACCATATTG	84132
rs549247556	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156630	TACGTGGCTAATTAG[A/G]TAAGAATTGTGCGTG	84132
rs549248105	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152545	CTCTGTTAGGAGGGC[G/T]TAGATATTAAACCGG	84132
rs549285941	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104008	AACATCGCTTGAGCC[A/C]GGGAGGTCGCAGCTG	84132
rs549286344	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135561	GAGGCTGAGGCAGGC[A/G]AATGGCTTGGACCCG	84132
rs549290277	in-del	-/AT	0.0605117	0.163077	intron-variant	USP42	GRCh38.p7	7:6090804	TAATATATATAACAT[-/AT]AGTTATATATATAGT	84132
rs549346993	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133821	CACCGCACCTGGTGC[A/G]TTTTTCATCCCAGAG	84132
rs549472763	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083618	TATACCCAGAAACCG[C/T]AATAAATATATGTAA	84132
rs549484702	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119761	GGCTAGAGTACAGTG[G/T]TGCACAGTCAGAGCT	84132
rs549512996	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089821	CAGGTGTGAGCTACC[A/G]CGCCCAGCCTCTTCA	84132
rs549514281	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6113128	CAGGCTGGTTTCAAA[C/T]TTATAATCCACCCGC	84132
rs549603684	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141293	CTGCAACCTCCACCT[C/G]CCGAGTTCAAGCAAT	84132
rs549632570	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6134308	CTGTGTTATTTCTGG[A/G]TCTTTTTCTGTTTAT	84132
rs549660577	snp	A/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6158552	TCCTTAGAGTGTGTG[A/T]GAGAGAGCTGGGGGT	84132
rs549684939	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6109349	ATTAAGATGTTGTGC[C/T]GTGGGCAGTTGGGCC	84132
rs549735398	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114585	GTTCATATTTCTCTG[A/G]TTGTTGTTTTATGTA	84132
rs549747328	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109041	GCCAGCACAGTACCG[C/T]AGAAATCAGCACAGG	84132
rs549788598	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094010	TTCTCCTTCCTCAGC[C/T]TCCTGAGTAGCTGGT	84132
rs549797314	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095384	TAAATTAAATGGCCA[C/G]AGGGGCCGGGTGTGG	84132
rs549799366	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6146749	ATGAGTTTGCTCCGC[A/G]TCGCACTCTGTGGCC	84132
rs549803521	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6145148	ACCAGCCTAGCCAAG[A/G]TGGTGAAACCCCTGT	84132
rs549910215	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158666	GTGAGGACGGGTTGC[C/T]TGCGGGCCTTGTAGA	84132
rs549913007	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6112827	GTGTGGCCCAGGGAA[A/G]CCAAAAGATTGGACA	84132
rs549913764	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6084164	CCTGAGTAGCTGGGA[C/T]TACAGGCATGAGCCA	84132
rs549936520	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124027	ATTACAGACATGCGC[C/T]GCCGTGCCCGGCTAA	84132
rs550007416	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161484	TGATCTTTGTTTTTC[C/T]AAAGATTAAAAAAGC	84132
rs550028459	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6089538	CACCTGACTTTCTCT[C/T]TTTTTTTTTTTTGAG	84132
rs550032510	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125370	TGGCAGATGCCTGTA[A/G]TCTCAGCTACTTCGG	84132
rs550074155	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088191	CTCCAGTGCACTCCA[G/T]CCTGGGCAACAGAGT	84132
rs550083156	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077026	ATTACAGGCACATGC[C/T]ACCACGCCCAGCTAA	84132
rs550130625	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123460	CGAGCTCAGGAGATC[A/G]AGACCATCCTGGCTA	84132
rs550131803	in-del	-/GT	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6135416	CTTTGGGAGGCCAAG[-/GT]GTGGGTGGATTGCCT	84132
rs550138186	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6127867	ACATCTTTACTATGT[C/T]CCTGAAGTCTGCTTT	84132
rs550140129	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6139378	TGGTTGAAATTTACA[C/T]GTGTGTCTTACGTAA	84132
rs550190137	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6158200	TTGGGGCGCAGCCAG[G/T]TGCGTTCCCACGCTG	84132
rs550201952	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133345	GGGCAACTTAAAATT[G/T]TCCCATAGCTTACTG	84132
rs550206866	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153258	AGCCTGGGCAACAGA[A/G]TGGGACTCTGTCCTT	84132
rs550233464	in-del	-/A/AAA	0.410521	0.193876	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153302	AAAATGAAACAAAAC[-/A/AAA]AAAAAAAAAAAATAG	84132
rs550244131	snp	G/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081575	GGGGCGGAGCCCGCC[G/T]CAGACCCCGCCCCTT	84132
rs550250524	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099562	TATGTTGGGCAGGCG[A/G]GTCTCAAACTCCTGA	84132
rs550265218	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132920	TTGTGATCTGCCCAT[C/G]TTGGTCTCCCAAAGT	84132
rs550282394	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156701	AAGCTCCAGGGTCTG[C/T]TGCTGGTGGTTTTGT	84132
rs550293222	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6107938	TGAGTTCAGAAACTT[A/T]AAGATTGTATTTTTT	84132
rs550330105	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6105869	ACTTTTGTTAATGAC[C/T]CTTAGGAGGCCGTGG	84132
rs550404867	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081614	CGACTGGGCAGGCGG[A/G]GCAGGAGGGGCGGCT	84132
rs550416591	snp	A/C	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6086438	TCTCGATCTCCTGAC[A/C]TCATGATCCGCCCAC	84132
rs550424363	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6149508	AAAATGGGAAGGACC[C/T]ATCAGCCAAAATGGG	84132
rs550437026	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115221	TAGGCTGGTCATGAG[A/G]TTTCGGATCTTGTAA	84132
rs550444398	snp	A/C	0.000399281	0.0141238	synonymous-codon	USP42	GRCh38.p7	7:6154350	CGCGGCGCCGAAAGC[A/C]CCAGGCCCTTCCCCA	84132
rs550472878	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157862	TGCCCTGTGGGGCTG[C/T]GTCTCCGTCCTGTGG	84132
rs550476802	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6123026	GATGGGGTTTCGCCC[A/G]TGTTGGCTAGGCTGG	84132
rs550540567	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136255	TTGATCCACCTGCCT[C/T]CGCCTCCCAAAGTGC	84132
rs550555357	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143530	CCTATTTTAAGAAAG[C/T]TCTTTTGTATGTTTT	84132
rs550560596	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094031	AGTAGCTGGTGCGTG[C/T]CACCACACCCGGCTA	84132
rs550577738	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106171	CTTTGAATCAAGTCT[A/G]CAGTAAGTATTTGGT	84132
rs550589845	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141189	TTACTCTTTGAATTT[C/T]CTTTTTCTTTTCTTT	84132
rs550605662	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086821	GACCTCTGTCTCCCA[G/T]TTCAAGCAATTCTCC	84132
rs550616901	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6148328	GGCAACAGAGTGAGA[C/T]CCCGTCTCCAAAATA	84132
rs550665728	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104668	CCCTTTCGCCGGCGC[C/G]CAGACGCGCGACCAG	84132
rs550670477	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6160632	TCTGTTCCAATCTGC[A/G]TGGTGCTTCTTTAGT	84132
rs550686334	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126590	GTGCCGGCCTGATAA[C/T]GCCACAGTTTCTTTA	84132
rs550693175	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6117646	AGGGATTGCAGTGTT[G/T]TATAGTCCCACCACT	84132
rs550713438	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6092574	AAGTATTACCTTCCT[C/T]ATTTGAGGCATCATG	84132
rs550714999	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106541	TGAAGTCTCATTCCT[C/G]CACACAGATCCAACC	84132
rs550740528	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142477	TGCCTTGGCCTCCCA[A/G]CGTGCTGGGATTACA	84132
rs550752939	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147338	CGTGGTGGTGCATGT[C/G]TGTGGTCCCAGCTAC	84132
rs550757528	snp	A/C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6132163	ACTCCTAGGCTCAAG[A/C/G]GATCCACCCGCCTTG	84132
rs550771404	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131776	TCTCTTTCTCTTTCT[A/G]CCTTTCACAGCCTTT	84132
rs550774414	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138057	TTTAAGAAAATGTCA[C/T]TGCTCTGTGTGTGTG	84132
rs550794687	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144308	ACAAAATTGCTAACT[A/G]TTACCTACATTTGGG	84132
rs550801894	snp	C/T	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6124296	TTTTTGAGACGGATT[C/T]TCGCTCTGTCACCCA	84132
rs550852770	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160277	AGGCCCAACCCTAAT[C/T]AAGGAGCTAAACTTC	84132
rs550865333	in-del	-/AT			intron-variant	USP42	GRCh38.p7	7:6078870	CTTAGGTCAACTAAC[-/AT]ATTTTAAATGTCAGT	84132
rs550919840	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6140619	TAGGATGAATTCTTA[A/G]TATTAGAATTTCTGG	84132
rs550923884	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110680	AGATTTTTTCTGTGT[A/T]GTTGATGCTTTTCTC	84132
rs550935940	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142868	CAGCCTGGGTGGCAG[A/G]GCAAGACCCAAACAC	84132
rs550941725	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117769	TGGTAGTATTTTGTT[A/G]TGGTTTTAATTTGTA	84132
rs550943572	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6111578	GTTTTTAGTTGCTAG[A/G]ATATTATTAGTTTCT	84132
rs550944641	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6160392	TGAGCTGCCCGCACC[A/G]CCAGTTCCCTCATTT	84132
rs550988498	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6151243	GGGACGGTACACTAC[C/T]GTAGACTCTGGAAAC	84132
rs550990235	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6127454	GTGATCCATTTTGAG[-/T]TTTTTTTTTTAGAAA	84132
rs550990381	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6096719	AGATCCTCCTTGTCT[G/T]CTTACAATGATATAT	84132
rs550997416	snp	C/T	1.65745e-05	0.00287871	missense	USP42	GRCh38.p7	7:6147809	CAGTCCTCTCCCCGC[C/T]CCGTCATCAGTCAGC	84132
rs551055642	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6096193	TATAGGTATACCTGG[C/T]CAGGCGTGGTGGCTC	84132
rs551058924	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6160058	CACTTCACACAGCGG[A/T]CCTGGGAGAGTCACT	84132
rs551085753	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6124649	TTATTTTGAGGCATT[A/G]TACCTTTTACATTTA	84132
rs551101331	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152230	GCTCAGAGTGCGGCC[A/G]GATGTCACCATACTC	84132
rs551121281	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120996	AGATTTTGATCTTAT[A/G]TCTTGGAACCTTAAG	84132
rs551121351	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114828	CCCTAGTAGCTAGGA[C/G]TACAGGTGCCCGTCA	84132
rs551184856	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120619	CCATCTTTAGTTTCT[C/T]GTTGCCCAGGCTGGA	84132
rs551252016	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6098941	AAAGAGTTCAGAGGA[C/G]CTTGAAGTTCTACGG	84132
rs551260088	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105612	GCCTAGCCACCTGGC[C/T]GCTCCGTGGAGAGTC	84132
rs551297787	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097565	GCATAAGCCACTGCG[C/T]CCAGCCATGTGGGTT	84132
rs551339160	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084996	AGTGCTGCGATTACA[A/G]GTGCGAGCCACCGCA	84132
rs551386896	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089897	CTTGCTGTGGCTGGG[C/T]GCAGGAGGCGCCAAT	84132
rs551423292	snp	A/C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6125038	ATACAAAAATTAGCC[A/C/G]GGTGTGGTGGCTCAT	84132
rs551442303	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158650	GGCACCAGCACTGCC[A/G]GTGAGGACGGGTTGC	84132
rs551450030	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103946	AAAATTAAGTGGGCG[C/T]GGTAGCGCGCGTCCG	84132
rs551479853	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6158374	GTTCACGTGTGAAGC[A/G]CATCCCCTCCTCCCA	84132
rs551519148	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6083370	AAGCAATTCTCCTGC[A/C]TCAGCCTCTCAAGTA	84132
rs551530025	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079330	CGGCGGGGTGGCACG[C/T]GCCTGTAATCCCAGC	84132
rs551592398	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6085771	TGGCATGTGCCATCA[C/T]GCCTGGCTAAATTTT	84132
rs551618637	snp	C/G	0.0115144	0.0749975	upstream-variant-2KB	USP42	GRCh38.p7	7:6078095	GCAGTGAGCCGAGAT[C/G]GTGCCATTGCACTCC	84132
rs551636315	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159806	CAGCGGCAGAGCCCA[C/T]GGGCCTTTGATAAAC	84132
rs551646921	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6156096	TCTTGAAAATGACGT[A/G]TCCATGATGAGATGG	84132
rs551649950	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108889	GGTGCTAAAAGCAAA[C/T]GCTAGTTGTTTTCTG	84132
rs551672896	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086977	GGGTGATTTGCCTGC[C/T]TCAGCCTCCCAAAGA	84132
rs551679751	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	USP42	GRCh38.p7	7:6077689	AATAGGGTGAAACTC[C/T]GTCTGTACTAAAAAT	84132
rs551737498	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138792	TCCATGCTCCTTAGG[A/G]GAATCTCATGCCTGA	84132
rs551757486	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119706	TTTGTTGTTGTTGTT[A/G]TTTTGTTTTTTTTTA	84132
rs551805243	snp	A/G	0.00597247	0.0543191	intron-variant	USP42	GRCh38.p7	7:6082388	CTGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC	84132
rs551856470	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6113059	CAGGTGCGCGCCACC[A/C]TGCCCAGCTACATTT	84132
rs551869316	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088944	GTCTCACCAAATGCC[A/G]TGAAGGGCCATAGGG	84132
rs551898167	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6118439	AGGTGGGAGGATCAC[A/G]TGAGCCCAGGAGGTT	84132
rs551913167	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6095297	CTTTAGAGCTGCGTT[A/G]ACTTGGACTCTGTAA	84132
rs551932121	snp	A/G	1.65765e-05	0.00287888	missense	USP42	GRCh38.p7	7:6149912	GAACGCATCTACGAT[A/G]TCAGTTTCTAGTAAA	84132
rs551953393	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134188	GAGCCACCAGGCTCA[A/G]CCACCATGTTTCTTC	84132
rs551988616	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141215	TCTTTTTTTTTTTTT[C/T]TTTTTGAGATGGAAT	84132
rs552011807	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098590	CTCACTCTTAACTGT[C/T]GCCCAGGCTGGAATG	84132
rs552030458	snp	C/G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108543	TGGAGTGCAGTGGCG[C/G/T]GATCTCAGCTCACTG	84132
rs552031820	snp	A/C	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6133683	TGCCACCACACCTGG[A/C]TAATTTTTGTATTTT	84132
rs552052051	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6143959	TGAAGGCTGGTGGTT[C/T]TCATCCAGTGTCCTT	84132
rs552086737	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114106	GGTCATAGGTAGTCT[C/G]CTCACAAGTGTGTAC	84132
rs552119070	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107285	TTGTTAGTGATTGTT[C/T]TGAAGGTATGTTTAT	84132
rs552148374	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6119989	TTTGTTTTTTGAGAC[A/G]GAGTCTCGCTCTGCC	84132
rs552191417	snp	C/G	0.00755907	0.0610114	intron-variant	USP42	GRCh38.p7	7:6105647	GTGCCCACGCCGGGC[C/G]GAGCGGCCACCCCGA	84132
rs552235255	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106511	GACTAGTATTTAAAG[A/C]AAAGGAAACACTTGT	84132
rs552259321	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092783	AGCCACAGTCTCAGA[A/T]TTCCTTCCTAGGAGA	84132
rs552296574	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6106125	ACTTATTTGTTTTAA[A/G]TTAGGGTCAGTTTCA	84132
rs552301889	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6132299	CCTGATAAGAAGTCT[A/G]TTGTCGTTTTTACCT	84132
rs552312622	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122931	CAAGTTCAAGTGATT[C/G]TCATACCTCAGCCTC	84132
rs552313779	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6120047	CTCGGCTCACTGCAA[A/C]CTACGCCCCCGGGTT	84132
rs552325494	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081523	AGCCCTTCTCCAGAC[G/T]TAAGACCCGCCCCAC	84132
rs552372277	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122589	GATTCTCCTGCCTCG[A/G]CCTCCTGAGTAGCTG	84132
rs552541106	snp	C/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6132832	GCGTGCCACCACACC[C/T]GGCTAATTTTTTTGT	84132
rs552615505	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6137953	CAAAGTGTTGGAATT[A/G]CAGGTGTGAGCCACC	84132
rs552640140	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6102309	AGTAGAGACAGAGTT[C/T]CAGCATATTGGCCAG	84132
rs552647175	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079248	CGGATCACAAGGTCA[G/T]GAGATCGAGACCACC	84132
rs552716382	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6097740	TGACTACAGGCGGCC[A/G]CCACCATGCCCCGCT	84132
rs552718436	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105716	TGTGTGCCTCTCTAG[C/T]GTTTTTTATTTTCGG	84132
rs552772370	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6151983	CTGTACTTTGTAAAG[A/G]CCCTTCAAGGATTCT	84132
rs552830187	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104741	TCTGGTGACGCGCGA[C/T]GTCTGCCTTCGCCCA	84132
rs552840046	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081076	AGAGAGTCTTGTACC[C/T]AATACCATTATTTGC	84132
rs552843446	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093237	TCCCTCCCTCCCTCT[C/T]TTCCTCCTTCCTTTC	84132
rs552866995	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127185	CATGTTCTTTGTTGT[C/T]GTACTGTCAAGTTTT	84132
rs552874304	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6131536	AATACACACAGAAGC[C/T]GAAGTAGAGCAATGA	84132
rs552885014	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157587	GTTTTTAGTAGAGAC[A/G]GTGTTTCACCGTGTT	84132
rs552889844	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6115841	GCTGGGCTCACACCT[A/G]TAATCCCAGCACTTT	84132
rs552975330	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152339	AGCATGAGCGACTCT[A/G]GATTTATATACTGGG	84132
rs552980217	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6152042	AATTTAAAAAAAAAA[-/G]TCATGTCATGTTAGT	84132
rs552998567	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141359	AGGTGCATGTGCCAC[A/C]ATGCCCAGCTAATTT	84132
rs553036342	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146980	CACCCGCACCCAGCT[C/G]TGTCCTGTTGTGGCT	84132
rs553044608	snp	A/G/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6129878	AAAAAAAAAAAAAAG[A/G/T]TTTCTTTTATATACA	84132
rs553069718	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6110833	ATGTCCAATTATAAA[C/G]TGAAATGCCAGACTT	84132
rs553078981	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135067	AGTGCTGAGATGATA[C/G]GCATGAGCCATGGCG	84132
rs553104752	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159571	GGAGTTTTAATTCTG[C/T]GGCTCTGCCTGGGGG	84132
rs553248694	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6136352	AAAAAAACCGAACCC[A/G]TCATGTATTAGAAAA	84132
rs553253407	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6147515	CTTCAGAAAACACAG[C/T]TTAAAGAACGTCATT	84132
rs553263169	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142521	ACGCCCGCCCGGAAA[A/T]TTTTCTTTTTACATA	84132
rs553298600	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095874	CTCAAGCAATCCTCC[G/T]GCCTCAGCCTCCTGA	84132
rs553322552	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141973	AATTCTGTTGAGACC[C/T]TTCTGTGTGAGCGTG	84132
rs553359502	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130142	AGGCATGAGCCCCCG[C/T]GCCTGGCCATGGATA	84132
rs553360834	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103428	GTAATCCCAGGTACT[A/T]AGGAGGCTGAGGCAG	84132
rs553375418	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6090071	TTGGGAGGTCAAGGT[A/G]GGCAGATCACCTGAG	84132
rs553376234	snp	A/G	0	0	intron-variant	USP42	GRCh38.p7	7:6134589	TGACTCTTTGCTGGG[A/G]GGGGCTGTCCGGTGC	84132
rs553422195	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109068	CAGGGTGCTGTGGGG[A/G]CCTTGAGGAGGGGTT	84132
rs553502868	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091081	TGTGTTCTTCATTAA[A/G]TCCTCCAACTTACTT	84132
rs553539530	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130594	CCTAGTCAGCCTTCT[C/T]CACCGTTAACCCAGT	84132
rs553548701	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6108636	CAGACACGCACCACC[A/G]TGCCCAGCTAATTTT	84132
rs553559550	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133915	TTTTTTTTTGAGACA[A/G]CGTCTTGCTCTGTCG	84132
rs553598074	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125161	ACTCCAGCCTGGGCA[A/G]CAGAGCGAGACTCTG	84132
rs553612216	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124759	TCTTTTAAAATCTTT[G/T]TCCTGCCTTCTTTTG	84132
rs553701240	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6094631	TCCAGTTTTTGCAGG[G/T]GTCAGACTGGTAAAT	84132
rs553715615	in-del	-/CTTA	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6155555	ATTGGTGTTAATATT[-/CTTA]CTTGTCAGATGTAGT	84132
rs553718132	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6150788	GTGTTACTGGCACGC[A/C]TTCAAGTGCCATCTC	84132
rs553739913	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6092662	TGGAAAGTAGGCACA[A/G]CATCTCCAATGACCC	84132
rs553756379	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158527	GCATTGTTGATTGAG[A/G]GGTAAACGGTCCTTA	84132
rs553761080	snp	A/G	0.000177321	0.00941429	synonymous-codon	USP42	GRCh38.p7	7:6154881	GCCGGCCCGGGAGAG[A/G]GAGCGGCACCGCCCC	84132
rs553812634	in-del	-/AA	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6093828	GGTTGTAAAATCTAT[-/AA]GAGTTAAAAGACCTT	84132
rs553814866	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088624	CTCATCCTGCCAACC[C/T]CGATTGACGTCACTA	84132
rs553861444	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080773	CCAAATACGTCTTGG[A/G]GGAACTTCCTATGTC	84132
rs553861504	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087710	GAATCTTCTCCAACA[A/G]CTATTTGAGATAAGC	84132
rs553917396	snp	A/G	3.78594e-05	0.00435066	missense	USP42	GRCh38.p7	7:6154207	GCCCGGGACGCTCAG[A/G]ACCCATCCCAGAGCT	84132
rs553918808	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6136824	TTTTTTTTTTTTTTC[A/G]AGTGAGACTGTGTCT	84132
rs553953032	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6113409	TGCTGGGGCTTCTCT[C/T]TCTTCTTAGGACTGA	84132
rs553965703	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107620	CTCCATGTTGGTCAG[A/G]CTGGTCTTGAACTCC	84132
rs554024266	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6082169	AGTCTCGCTTTGTCG[C/T]CCAGGCTGGAGTGCA	84132
rs554051685	snp	A/G	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6154598	AGCGCCGCTCTCTGG[A/G]CAGGTGCAGTCACCA	84132
rs554056483	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6139641	TCAAGAGGAAGAACG[A/G]GGGGACAGATAATGC	84132
rs554060160	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080280	AAGTTTCCCTCCCCT[A/G]TTGACTGTTGGCAGT	84132
rs554075702	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106909	ACTTTTATATATCAT[C/G]AGAAGCTGTTGCTTA	84132
rs554095856	snp	A/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6108860	TACTGTATGTTAATC[A/T]TTCAGCACAAGCTGG	84132
rs554107407	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083752	TATTGTCTTCCAGTA[C/T]GTTGTTTTAGGAACT	84132
rs554107465	snp	A/C	0.0023933	0.0345097	upstream-variant-2KB	USP42	GRCh38.p7	7:6077227	TCCTTCATTTTGACC[A/C]CAGCTCTTACGCACC	84132
rs554119658	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6082699	CACTGCAACATCTGC[C/G]TCCCAGGTTCAAGCA	84132
rs554129454	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112434	CAGCCTGGGCAACAG[A/G]GTGAGACTCTGTCTC	84132
rs554141651	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118159	AGCACTTTGGGAGAA[C/T]GAGGCAGGTAGATCA	84132
rs554172616	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148624	CCCTGTTGGTCCTGT[C/T]GGGGCGAACAGTAGT	84132
rs554206555	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148423	AAGCCTGGGTGTCAG[C/T]ACCTTTAAATTTTAG	84132
rs554217282	snp	C/G/T	0.00109353	0.0233578	synonymous-codon	USP42	GRCh38.p7	7:6153948	CATGGCCGTCGCCCC[C/G/T]GAGGAGCCTCCGCCC	84132
rs554226515	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6098374	CTTGATCTAGGCCCC[A/G]TAGTATCCATTCCCG	84132
rs554254281	snp	A/C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6157682	ATACGTTACTCTCCC[A/C/G]AATCCTTAAACCTGT	84132
rs554294523	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161705	CCATCCCACCTCGGA[C/G]GGGCAAAGGAAAATT	84132
rs554312726	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087223	TTTTAGTAGAGAAGG[C/T]GTTCACCATGTTGGC	84132
rs554316212	snp	A/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6137036	TTTTAAATGGGTAAG[A/T]GCATGAAATTTTCTT	84132
rs554320793	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6118864	GGACTCTATTATGTT[A/G]TACTGATCACTTGTT	84132
rs554329765	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6133631	GTGGTCCTCCCATCC[C/G]ACATCAGCCTCTGGA	84132
rs554395156	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138981	TTTCCTCATAAAGTA[A/T]GTATTTGGGAGTTTT	84132
rs554422535	snp	A/G	0.00597247	0.0543191	intron-variant	USP42	GRCh38.p7	7:6157384	GTTTGGTTTGGTTTT[A/G]TTTTATTTTATTTTA	84132
rs554435551	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime	USP42	GRCh38.p7	7:6160944	ACAGTGTGTATATTT[A/T]ATTTAAAGACTTATT	84132
rs554441297	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6093410	CATGCCTCAGATTCC[C/T]GAGTAACTGGGACTA	84132
rs554451199	in-del	-/T	0.44252	0.159487	intron-variant	USP42	GRCh38.p7	7:6096932	TCTTTCTTTCTTTTC[-/T]TTTTTTTTTTTGAGA	84132
rs554466909	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144973	TGTTAAAAGAAAATA[A/T]TAAATGCAGCAGGAT	84132
rs554508487	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132950	TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC	84132
rs554528389	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144585	TATTAAAATTAAATA[A/C]TCGGCCGAGTGTGGT	84132
rs554536010	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6137743	GGAGTGCAGTGGTGC[A/T]GTCTTGGCTCACTGC	84132
rs554582773	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131523	ATATACAGAAAAAAA[A/T]ACACACAGAAGCTGA	84132
rs554596967	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6097000	ATGATCTTGGCTCCC[A/G]GGTTCAAGTGATTCT	84132
rs554626339	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6105809	GACGGAACAAGTTTT[C/T]CCATCTAGGACTTTA	84132
rs554682856	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120337	AACCTCCACCTCTTC[A/G]GTTTAAGTGATTCTC	84132
rs554682894	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6095287	CCTGAGGGTGCTTTA[C/G]AGCTGCGTTAACTTG	84132
rs554690868	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104705	CAATCAGCGCGCTCC[C/G]TCTGCCGGCCCGACC	84132
rs554733608	snp	A/G	0.000138363	0.0083164	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111203	CAGCCTGGCAGCTCC[A/G]AGGCAGTCTCACCTG	84132
rs554774858	in-del	-/T	0.273587	0.248885	intron-variant	USP42	GRCh38.p7	7:6141564	AGTTGGTTATTATTA[-/T]TTTTTTTTTTTTGAG	84132
rs554784235	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127455	TGATCCATTTTGAGT[C/T]TTTTTTTTTAGAAAC	84132
rs554799016	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6122309	TTTTTAAAGACAGGG[G/T]CTCACTCACTCTGTT	84132
rs554814458	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6097237	TGCCCTCCGTGGTCC[C/T]GGTAAAACGGTGTTT	84132
rs554820382	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132603	ACCTCAAGTGATCTA[C/T]CCGCCTCAGCCTCAC	84132
rs554868988	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077164	AGGCGTGATGAGCCA[C/T]CGTGCCGGGCCACCA	84132
rs554893930	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6099276	CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCATT	84132
rs554931049	snp	A/G	0.0107246	0.0724382	intron-variant	USP42	GRCh38.p7	7:6121283	TGTTGTAGGTTTTTC[A/G]TAGATGCCTTTTACC	84132
rs554934175	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114397	AACTCTCATGTAGCC[A/G]TCAACCAACTTTGAC	84132
rs554941362	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6152423	AGTTTTTACCCGCAC[A/G]GTTGTTGGCACTCAC	84132
rs554953244	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6159968	CCCCCCAGCAGCCAC[C/T]GTACAAAACCATAGG	84132
rs554957905	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079534	TTCATTAAATATGAG[C/G]TATGTAACATAGATA	84132
rs554977873	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156504	GCCCAGGCTGGAGTG[C/T]GGTGTTGCAGTCGTA	84132
rs554998531	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6108573	GCAACCTCCACCTCC[A/C]GGGTTCAAGCGATTC	84132
rs555001094	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6136346	CTGGTGAAAAAAACC[A/G]AACCCGTCATGTATT	84132
rs555033524	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097684	CAAACTCCGCCTTCC[A/G]GGATCATGCCATTCT	84132
rs555040180	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	USP42	GRCh38.p7	7:6084461	GCCGGACACTAAAGG[A/G]CATCACTCTGAGCCT	84132
rs555051271	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127813	GCTGGGATTTTGATA[A/G]GAAGTACACTAAACT	84132
rs555053235	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6090014	TCAAAAGATATATAT[A/G]TAGGGCCAGGCGCAG	84132
rs555058499	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142502	ATTACAGGCGTGAGC[C/T]ACCACGCCCGCCCGG	84132
rs555072295	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120187	GCCAGGATGGTCTTG[A/T]TCTCCTGACCTCATG	84132
rs555084149	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6107349	TGTTACTGTAAATAA[A/G]GCTGGATTAACCTTT	84132
rs555145582	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155383	AAAAATTTGCCCTGC[C/T]TTGAAGCTGTATCTT	84132
rs555165485	snp	C/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6109733	TGAGACTTAATCTTG[C/T]TCTGTCACCAAGGCT	84132
rs555183240	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152757	ATATCGAAAGCTCTG[C/T]GGGAATCAAAGGACA	84132
rs555234904	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080056	GTGAAACCCCGTCTC[C/T]ACTAAATGTACAAAA	84132
rs555305525	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155778	TTTTTAAGAGACAGG[A/G]TGTTGCTCTGTCACC	84132
rs555316611	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6160350	GGGCGGGTGGTGGCC[A/G]GGCCCAGCAGATGGC	84132
rs555442048	snp	C/T	9.0712e-05	0.00673408	synonymous-codon	USP42	GRCh38.p7	7:6150134	CGAAGATGAGGAGGC[C/T]ACTCCGCACGAGCTT	84132
rs555505068	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6145846	AGACTGAGGCTGGGG[G/T]ATCACTTGAGGTCAG	84132
rs555596783	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	USP42	GRCh38.p7	7:6077171	ATGAGCCACCGTGCC[A/G]GGCCACCAGGGCCTA	84132
rs555650671	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079206	GCTCATACCTGTAAT[C/T]CCAGAACTTTGGGAG	84132
rs555687577	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146907	AGCACCTGGCGTGGT[C/T]ACAGCCAGCACCTCC	84132
rs555723966	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146531	TAGCCAGGTGTGGTG[G/T]TGTGGGCCTGTGGTC	84132
rs555724216	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151949	GGTCTGTTGTTGACC[A/G]TATGTATGAGGTACA	84132
rs555783112	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133512	GGTGTTTTTGTTATT[C/G]TTGTTTGTTTTTATT	84132
rs555791081	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6133062	TCATGTTTCTACTCC[C/T]GGAATTTGTTGAGGT	84132
rs555798637	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140662	GTGTATTGTAAATTT[G/T]AATTCTGTCAGGTTG	84132
rs555811956	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113722	CGCCTCCCGGGTTCA[A/C]ACCATTCTCCTGCCT	84132
rs555820379	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108249	GATGCTTTTAAAAAA[C/G]AAATTTGGCCAGGTT	84132
rs555848955	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6129425	AGCCAGGCATGGTGG[A/C]GGGCGCCTGTAATCC	84132
rs555855471	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6142362	GCTGGGACTACAGGC[A/G]CGTGCCACTGTGCCC	84132
rs555909290	snp	C/T	0.00676609	0.0577691	intron-variant	USP42	GRCh38.p7	7:6124278	TAGATTCCCTTTTTT[C/T]TTTTTTTGAGACGGA	84132
rs555941287	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138871	GAAAAATGGTCTTCC[C/G]TGAAACCAGTCCCTG	84132
rs555964471	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135018	TAGTCTCAAACTCTT[C/G]GCCCCAAGAGATGCA	84132
rs555973222	in-del	-/TTTTTG	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113612	TCAGCCTTTTGGTTT[-/TTTTTG]TTTTTGTTTTTGTTT	84132
rs556000424	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6144915	ATTTTGTTAGTCTGT[C/T]CTTTGATGGGTTTGA	84132
rs556038611	snp	A/G	7.76277e-05	0.00622959	missense	USP42	GRCh38.p7	7:6154272	TCCTGTGCTGGACAT[A/G]GCCCCGGCCGGTCAC	84132
rs556038941	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129581	AAAAAAAAAAAAGGA[C/T]GAGGCGCGGTGGCTC	84132
rs556047257	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134470	TATTGCAAGACAGAG[C/T]TAATTGGGAATAGCT	84132
rs556115003	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6082580	CAACATAAGGAGACT[A/G]CGTCTCTATTTTCTT	84132
rs556116895	snp	A/C	0.00795532	0.062565	intron-variant	USP42	GRCh38.p7	7:6145300	CGTGTCACTGCACTC[A/C]AGCCTGGGTGATAGA	84132
rs556135301	snp	A/C/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113690	GCAGTGTTGCAATCT[A/C/T]GGCTCACTGCAACCT	84132
rs556228071	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6087126	AACCTCTGCCTCCCA[C/T]GTTCAAGCGATTCTC	84132
rs556237446	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6138477	TGAGACAAAACAGCC[A/G]GTTTATTCAAGTGTA	84132
rs556267933	snp	A/G			utr-variant-3-prime	USP42	GRCh38.p7	7:6161186	ATGATTTGTAAAGCC[A/G]ACAGTATGTTTCTAT	84132
rs556273846	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6100111	TCCGGCCTCAGCCTC[C/T]TAAAGTGCTGGGATT	84132
rs556277606	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6140092	CTGGAGTTTTTGCAA[A/G]GCTCTTCTCTCATGT	84132
rs556279659	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093657	CCTTACCTCTTTCTT[C/G]CTTTCTCTCTTTTTT	84132
rs556352497	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112392	AGGCAGAGGTTGCAG[A/T]GAGCCCAAGATCGCA	84132
rs556377382	snp	A/G			intron-variant, missense	USP42	GRCh38.p7	7:6130256	GTGATGTCAGATGGA[A/G]TAGAAGCCCACATTC	84132
rs556378315	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6100001	CTACCAAATTTCACA[A/G]GTCTATTATTATTAT	84132
rs556384831	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086598	CAGGTGATCCACCCC[C/G]CTCAACCTCCCAAAG	84132
rs556464901	snp	A/C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6111795	TTTTTTTGTATTTTT[A/C/T]GTAGAGACGGGGGTT	84132
rs556487504	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089056	ATTTATTTATATTTA[C/T]CTTTTTGAAATGGAG	84132
rs556504198	in-del	-/TTTTG			intron-variant	USP42	GRCh38.p7	7:6122446	ATGCACCACCATGCC[-/TTTTG]TTTTGTTTTGTTTTT	84132
rs556584939	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126733	TGCAGTAAACACATC[C/T]GGGTTGTTTCTGGTT	84132
rs556589790	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6100832	CTACCACACTCAGCT[A/C]ATTTTTTGTATTTTT	84132
rs556616576	snp	C/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6157287	GACACAGGACTGAGG[C/G]CAGCACTACCTGTGT	84132
rs556702968	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092379	AGATGGGGTTTCACC[A/C]TGTTGGCCAGGCTGG	84132
rs556706919	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6135270	ATAATAACTCTTTGA[C/T]ATTGGGCAAACTTTT	84132
rs556712391	snp	A/C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6142573	ATCTTTGAGTCTTCT[A/C/G]TTCCTTCTTTTAAAA	84132
rs556771870	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147541	TCATTTACCCAGTTA[G/T]CCTTGTTGTCTCCTG	84132
rs556794274	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131012	CTGGCACCTGGCCCT[C/G]AGATGATTAGGGCAG	84132
rs556851328	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6160506	GGAATAAGCCCTACA[C/T]GCCGCCGCCTGCCTC	84132
rs556885858	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6149012	CTGGGAAGGCCACAC[A/G]TGATCTGTTAACTGA	84132
rs556893358	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148003	ATACATCTGAATTTC[G/T]TCTCACAGTTTAATC	84132
rs556898051	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148557	TAGGTCCATTTAGTC[A/G]TTTCAGGGGTGTGGT	84132
rs556918457	snp	C/G/T	0.00011449	0.00756532	missense	USP42	GRCh38.p7	7:6153905	GCGATCCCGGCACCC[C/G/T]CGCTACCAAAGAAGG	84132
rs556978589	snp	A/C	0.0865458	0.189163	intron-variant	USP42	GRCh38.p7	7:6135681	AAAAAAAAAAAAGAA[A/C]AAAAAAAAGTAAATG	84132
rs556989435	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6120602	ACTATGCCTGGCCTA[C/G]GCCATCTTTAGTTTC	84132
rs556990725	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135182	CCTTGCTTTTCCTGT[A/G]TAGAGAGTAGCTAGG	84132
rs557041859	snp	C/G/T	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6136892	AAGTGATCCTCTTGC[C/G/T]CCAGTTGAGTAGCTG	84132
rs557050497	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141409	GGGGTTTCACCTATC[A/G]GCCAGGATGGTCTTG	84132
rs557076744	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6117232	CCGGCAACCACTGAT[C/T]TGCTTTCCGTCACTA	84132
rs557093147	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156404	AGGATGGAGCTAAAG[G/T]TGGTGAATTTATGGC	84132
rs557130336	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6115926	CAACATAGTAAGACC[C/T]CATCTCTACTAAAAA	84132
rs557196892	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098302	CTGTATTAAAGGAAA[C/G]TGCCCACATATCTAT	84132
rs557197555	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131370	ATCCCAGCTACTCGA[A/G]AGACGGGTGGGGAGA	84132
rs557214628	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103654	GAGTGTAATCCCAGC[C/G]CTTTGGGAGGCTGAG	84132
rs557249398	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6086917	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	84132
rs557302481	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079277	CCCTGGCTAACACGG[C/T]GAAACCCCATCTCTA	84132
rs557335759	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125320	ATGGTGAAACTTTGT[C/T]TCTACTAAAAATACA	84132
rs557345449	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094984	GTAGAGATGGAGTTT[C/T]GCCATGTTGGCCAGG	84132
rs557355374	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6097162	TCCTGTTATTAGCCC[G/T]GGCTTATACATGACA	84132
rs557387675	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6152705	GCTGTGCAGACAAGC[C/G]CAGGCCACAGCAGCT	84132
rs557400853	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6096642	CAGGAGGCTGTGAAA[C/G]AGGCTGATTGCACAA	84132
rs557405369	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104227	AGCTGGGACTACAGG[C/T]GCGCGCCACCACGCC	84132
rs557436991	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095591	GGAGAATCACTTGAA[A/C]CTGGGAGGCGGAGGT	84132
rs557446110	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146889	CTCAGGAAGGGACCT[C/T]TGAGCACCTGGCGTG	84132
rs557467007	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096612	TCCAAGGTTTGGGGA[A/C]GAACAGGTGCAGAGC	84132
rs557480267	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6124155	TGCTGGGATTACAGG[C/T]GTGAGCTACCATGCC	84132
rs557534053	snp	G/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6125831	TTTTGTTTTTTTTTT[G/T]GTTTGAAATGTCTTT	84132
rs557541120	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129515	TGAGCCAAGATTGTG[C/T]TACTGCACTCCAGGC	84132
rs557561660	snp	C/T	0.00517822	0.0506191	intron-variant	USP42	GRCh38.p7	7:6089625	GCAACCTTCGCCTCC[C/T]GGGTTCAAACAATTC	84132
rs557570342	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6113429	CTTAGGACTGAACTC[A/G]CATCTCCCCACTCTC	84132
rs557589448	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120763	TAATTTTTGTATTTT[C/T]AGTAGAGATGGGGTT	84132
rs557619179	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109138	TGTCCCAGAGAAAGT[A/G]AAGTCTAAACTGAGA	84132
rs557631931	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159926	TGCTGTCTGCGCCCC[A/G]AGGTGGCACTGAGCT	84132
rs557675284	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6091889	ACAGCACTCTCAATC[A/G]GCATTTCTTCCTGAA	84132
rs557687437	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091271	GCTCTGTTGCCCAGG[C/T]TGGAGTGAAATGGCA	84132
rs557731626	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124587	GATTTCTTATAAATA[C/G]CTTATTAATTTGATC	84132
rs557769666	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077153	GCTGGGATTACAGGC[A/G]TGATGAGCCACCGTG	84132
rs557801201	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6082371	CTGACCTCGTGATCC[A/G]CCTGCCTTGGCCTCC	84132
rs557827757	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6113196	CACTGCACCCGGACA[A/G]CAGTAAGTTTCATAT	84132
rs557883498	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6158856	CTACTGGGAGACAGT[A/G]ATGGCCCCCGAGGCA	84132
rs557895405	in-del	-/CAAT	0.0146876	0.0844278	utr-variant-3-prime	USP42	GRCh38.p7	7:6161116	TGGAACTGTTCCAAT[-/CAAT]CAATCAATTTCCCAG	84132
rs557897626	snp	C/G	0.000116241	0.00762279	missense	USP42	GRCh38.p7	7:6150105	GTGAGCTCCCACTCT[C/G]CCGGCCAAGATGCCG	84132
rs557898382	snp	A/C	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6102395	GGGATTACAGGCGTG[A/C]GCCACCACGCCCAGA	84132
rs557898531	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6095027	TCCTAACCTCAAGGG[A/T]TCTGCCCGTCTGGGC	84132
rs557967440	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6109247	CAGCAGGGACAAAAG[-/A]AAAAAAAACAAGACT	84132
rs557984532	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081746	ACTGCGCCTACGTGG[A/G]CTGCGGGTTCGCTCC	84132
rs558007131	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101501	CAGGCAGCATTCACT[C/T]TGGATTACACTCTGA	84132
rs558030920	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6085137	TTTATTTATTTATTT[A/T]GAGACAGATTCTCAC	84132
rs558035240	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6078398	ATTAGGTCAGGAGAT[A/C]GAGACCATCCTGGCT	84132
rs558067596	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6108358	GCCTGGGCAACGTAG[G/T]GAGACCCTGTCTCTA	84132
rs558087650	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6087151	ATTCTCCTGCCTCAG[C/G]CTCCCGAGTAGCTGG	84132
rs558105011	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6155278	CACTCGACTCAGGAA[A/C]AAGTGACCAGCCAGG	84132
rs558126244	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6111398	TTTCAAAAGAGAGAA[A/T]TACCGCCAGAAACTC	84132
rs558150628	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6108299	TTCCAGCATTTTGGG[A/G]GGCAGAGGCAGGAGG	84132
rs558185503	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145303	GTCACTGCACTCCAG[C/T]CTGGGTGATAGAGTG	84132
rs558189055	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137749	CAGTGGTGCAGTCTT[A/G]GCTCACTGCAACCTC	84132
rs558207061	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119213	GAGTGAGATGCTGTC[G/T]CAAAAAAAAAGTTTT	84132
rs558208001	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108044	CAAAAATTAGCCGGG[C/T]GTGGTGGCACGCACC	84132
rs558250570	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143770	ATTATACCAGTCTGA[A/G]CATGTTCGTTTTTCA	84132
rs558262584	snp	A/G			missense	USP42	GRCh38.p7	7:6150268	CCCTGCACTCAGAAA[A/G]TCCCTTTGCTAAGGC	84132
rs558287537	snp	C/T	7.41262e-05	0.0060875	synonymous-codon	USP42	GRCh38.p7	7:6153969	GCCTCCGCCCAGCGC[C/T]GGCGAGGACATCGTG	84132
rs558315063	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129002	ATTTTTGTAGAGACA[C/G]GGTTTCACCATGTTG	84132
rs558349107	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106808	TGGGCTCAAGCCATC[C/T]TGCTGCCTTGGCCTC	84132
rs558350412	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6113043	CGAGTAGCTGGGACT[A/G]CAGGTGCGCGCCACC	84132
rs558368101	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134387	TTTGATTGGATGCCA[A/G]ACAGAATGAATTTTA	84132
rs558369987	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126667	ATCGTGAGTGGAGCT[A/G]CGGTAAACACATCTA	84132
rs558390061	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6112147	TTCGTAGTAATAAAG[C/T]TCTTTGAAAGAGAGC	84132
rs558413754	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112282	GGTGAAACCCCATCT[C/T]CACTAAAAATACAAA	84132
rs558423274	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157714	GCATTCTGAGTGCAC[C/G]CTGATGCTCGGTACT	84132
rs558435195	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6140483	TAACAGCCTTCGACA[A/G]TTGGAGTAGTGTTCC	84132
rs558448136	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6139750	TAGGACTTCATTGTC[C/T]GGGTGATGACATACT	84132
rs558483834	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128113	CCACCATGACCAGCT[A/C]ATTTTTTTATTTTTA	84132
rs558495129	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6130324	GGGATCGTTGTCCCT[A/G]CTGGGTGGAAGTGGA	84132
rs558497992	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6122126	TCTGCTTACTTTGGA[C/T]TTAATGTGCTCTGTT	84132
rs558504509	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6139008	TTTTCCAACCAACAT[A/G]TTATTATAAGATATA	84132
rs558509027	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6141591	TGAGATGGAGTCTTG[C/T]TCCATTGCCCAGGCT	84132
rs558509078	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133010	TTTTAAGATTTTTAT[C/G]ACTGGTTGTAAGTAG	84132
rs558511928	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6115915	ACCAACCTGGACAAC[A/G]TAGTAAGACCCCATC	84132
rs558520802	in-del	-/A	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6140471	GCACACAGGCCTAAC[-/A]AGCCTTCGACAGTTG	84132
rs558540517	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6079578	GCTAACATTGTTTGT[A/T]ATTAAGCTGCCTTGG	84132
rs558543216	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133437	TTCTACCCATAATGA[A/G]TATCTTCAAGTTCAC	84132
rs558552064	in-del	-/TC			utr-variant-3-prime	USP42	GRCh38.p7	7:6161085	ATTTTATAGACAAGT[-/TC]TGTTTTTGAACTTTG	84132
rs558556285	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093140	CCTTCCTTTCCTTTC[A/C]CTCCCTCTCTCCCTC	84132
rs558624400	snp	C/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077296	AAATGATACCCTTGT[C/G]AAGTTCCCTCTTACA	84132
rs558659878	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106311	GTGGATTACATTGTT[A/T]ACGAAGAAGCAGAGC	84132
rs558743369	snp	G/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081371	GGCCGCCGCGGGGAG[G/T]TAGATGGCGGGCGGC	84132
rs558772461	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6086082	TGACTCTCACCCAGG[C/T]TGGTTTGCAATGCCA	84132
rs558785369	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123363	CCCTCTCTGTATAAT[A/G]TAAAATATTAAAAAA	84132
rs558854262	snp	G/T	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6122247	AGTGGTACTTTAGTT[G/T]TATCCCAGATATGTT	84132
rs558858166	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116636	AAACTGATTTTTTTT[C/T]CCCTCCAAAGAGCCA	84132
rs558871135	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6150647	GAATTATAATGTATA[A/G]GATTTATTAACTTGC	84132
rs558881750	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094162	GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC	84132
rs558893989	in-del	-/T	0.499234	0.0195537	intron-variant	USP42	GRCh38.p7	7:6097907	TTTTTCTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	84132
rs558896237	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093468	CTTTTGTATTTTTTG[A/G]TAGAAACCAAAACCA	84132
rs558939173	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086516	AGCCTAGCCGGGCTA[A/T]TTTTTGTATTTTTAG	84132
rs559001216	snp	A/G	0.00557542	0.0525036	intron-variant	USP42	GRCh38.p7	7:6092264	CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	84132
rs559005905	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6152910	CAGAGAAAGGGAGTC[A/G]AGAGGAAAGGAGGAG	84132
rs559067519	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6111753	GACTACAGGCGCCTG[C/T]CACCAAGCCCGGCTA	84132
rs559089237	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160387	CTGGCTGAGCTGCCC[A/G]CACCGCCAGTTCCCT	84132
rs559201310	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097267	TTCCAGGCCTTGTGA[C/T]GGAATGTCACCAGCT	84132
rs559212093	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108842	TTTAAGGATCAAATG[A/G]TATACTGTATGTTAA	84132
rs559246555	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084898	TAATGTTTACATTTT[C/T]AGTATAGATGGGGTT	84132
rs559265594	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096675	TGATTAATCCCTGGA[A/G]ATTAATCCCAAGTTC	84132
rs559266920	snp	A/G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6109473	TCTCGGCTCACTGCA[A/G/T]TCTCTGCCTTCCAGG	84132
rs559290614	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080565	AACATAGTGAAACCG[C/T]GTCTCTACTAAAAAT	84132
rs559292178	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158616	TGGAGTGCTGGGGAA[A/G]CAGCCGGAGATGAGG	84132
rs559370563	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6117895	TTTGCTAAAATGCCT[G/T]TTGAAATCTTTTGCC	84132
rs559408928	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135372	AAGTAAATGAGGCTG[G/T]GGTGGTGGCTTACAC	84132
rs559419911	in-del	-/TCTTGCAGT	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6098428	TGTGTATTAGCCTGG[-/TCTTGCAGT]TCCTTCAATTTTTGA	84132
rs559441035	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6139990	CTTGGGCTGCCACAC[A/G]TGCCATCCTTTTATT	84132
rs559454012	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089450	AATACAGAAAATTTT[A/T]AAAACGTAATACATA	84132
rs559484964	snp	A/G	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6146606	GGAGGCCGAGGCTGC[A/G]GTAAGCCATGATTGA	84132
rs559501136	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118837	TAAGCCATATCAATA[C/T]GATCTATTTCTGGAC	84132
rs559507672	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6097841	GTGATCCGCCCGCCT[A/C]GGCCTCCCAAAGTGC	84132
rs559537747	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129253	TCCACTAGTTATAAT[C/T]GTTATAAAATGTTTC	84132
rs559544607	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6134108	GTGTTAGCCAGGATC[A/G]TCTCGATCTCCTGAC	84132
rs559544834	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6130890	TGGCCAGAGCCTTCG[C/T]TGAGGTTTCCGTGGG	84132
rs559557043	snp	G/T	0.000186168	0.0096462	intron-variant	USP42	GRCh38.p7	7:6135998	TATTTATTACCTAGT[G/T]ATACTTTTTTTTTTT	84132
rs559560480	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159795	AACCCGGCTCACAGC[A/G]GCAGAGCCCACGGGC	84132
rs559571708	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095138	CTGTAAGTCAAGGAA[C/G]CAGTTGCTAAGTATG	84132
rs559621667	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083284	TATTTTAGATACAGT[C/T]TAGCGCTGTGGCCCA	84132
rs559650527	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158987	CCGTCCCACTGCACC[A/G]ATGACAGGGTTTGCA	84132
rs559659877	snp	A/C	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6151015	GCGGCTCCTAGGCCA[A/C]AAACCTGCACAGCCT	84132
rs559686187	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6129636	GAGGCCGAGGCGGGC[A/G]GATTACCTGAGGTCA	84132
rs559687623	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113959	ACTGGGGGACTGCCA[A/G]AGCCTTTGAAAAATT	84132
rs559724358	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123435	TTGGGAGGCCAAGGC[A/G]AGCAGATCACGAGCT	84132
rs559786405	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6122897	GGTATGATCTTGGTT[C/T]GCCGCAGCCTCCACC	84132
rs559817737	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133783	CCTCAGCCTCCCGAA[A/G]CACTGGGATGACAGG	84132
rs559850358	snp	A/G	0.000309665	0.0124393	missense	USP42	GRCh38.p7	7:6154315	GCTGAGCCTAGCCCC[A/G]GCGAGAGGGTCGAGG	84132
rs559871143	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6127603	CATATTTGTGTGTCT[G/T]TCTCCAGGTTTCTGT	84132
rs559909584	in-del	-/AT	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6143742	AGATGAATTTAAGAC[-/AT]ATTTTCACATAATTA	84132
rs559928426	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6101845	GCACTTTGGGAGGCT[C/G]AGGTGGGCAGATCAC	84132
rs559995902	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6119936	TGAACTCCTACGCTT[A/C]AGCGGTTCTCTTGCC	84132
rs560027095	snp	C/G	0.000585813	0.0171045	missense	USP42	GRCh38.p7	7:6154706	GGGAGAAGTTCTACC[C/G]CGACAGGCCGCGCTG	84132
rs560035245	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088039	GCATGGTGGCTCATA[A/C]CTGTAATGCCAGCAC	84132
rs560057087	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124299	TTGAGACGGATTCTC[A/G]CTCTGTCACCCAGGC	84132
rs560061959	snp	G/T	0.0107246	0.0724382	intron-variant	USP42	GRCh38.p7	7:6119691	ATTTAGGCCTTGTTT[G/T]TTGTTGTTGTTGTTG	84132
rs560063707	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6149298	ATGCCACAGGTCCTG[A/C]TGATTTCGATCAGAT	84132
rs560133493	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106085	ACTCATTCAAATTGC[C/T]TAGGGGATATGAATG	84132
rs560221285	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6113037	GCCTCCCGAGTAGCT[A/G]GGACTACAGGTGCGC	84132
rs560244987	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6111474	TTTTGCAAGGCGTGA[A/G]GCCACCTGAGTGGCC	84132
rs560282476	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158121	TGGTTGGAAATAATC[C/G]CAAAGAACAATGCGT	84132
rs560334300	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100274	CTAGATGGGCGCCTG[A/C]TACTGTTGCCCAGCT	84132
rs560345657	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6101190	GGCAGCTGTGAGTTA[C/T]AAGCAGCGAACACCA	84132
rs560373833	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081219	CCCCGTATACCTCCG[C/T]TTTAAGATGAGAGAA	84132
rs560375749	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6107526	GGGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC	84132
rs560399163	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153539	ATAGCTGCTAAATGA[C/T]GAGTTAATGGGTGCA	84132
rs560406945	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107737	TTTCCTGCATTTTTT[C/T]CTTCTGTCCCCACAC	84132
rs560445056	snp	C/T	0.0345262	0.126772	intron-variant	USP42	GRCh38.p7	7:6092094	TTCCTCTTCTTCTTC[C/T]TCCTCCTCTTCTTCT	84132
rs560517172	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6160218	GAGTCTGTGGATTAA[C/T]TGGCCGTTAATTAAC	84132
rs560519884	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159432	ATTAAAATCTCTTTC[C/T]TGACCTTTGCTTTCT	84132
rs560563576	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143364	GACTTTCTTATGATA[A/C]GAGGGCTGCCGTCGG	84132
rs560565291	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148635	CTGTCGGGGCGAACA[A/G]TAGTGAGCTAGTGTC	84132
rs560578067	snp	C/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6148242	CTCAGGAGGCTGAGG[C/G]AGGAGGATCACTTGA	84132
rs560584836	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138583	ACTTTTAATGGTGTA[A/G]AGCAGGGGTCCCTAA	84132
rs560672191	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161333	TAATATGGATATGCT[A/G]TCAAACTGTGATACA	84132
rs560707360	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131965	TTTGAGACAGGCTGT[C/G]ACTCTCACCCAGGCT	84132
rs560714514	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6138687	TGAGCATCCCCACCT[G/T]AGCTCCGCCTCCTGT	84132
rs560724448	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6093325	AAGTCTCACTCTGTT[A/G]CCCAGGCTGGAGTGC	84132
rs560759003	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6093223	CCTTTCTTCCTTCCT[C/T]CCTCCCTCCCTCTCT	84132
rs560813268	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117298	TATGTGGAATTGTAC[A/T]GTATATATTCTCATA	84132
rs560813380	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6091738	GTTGCTGATTTAATA[C/G]TCTGGTAAAAAAATT	84132
rs560831181	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086607	CACCCCCCTCAACCT[C/T]CCAAAGTTCTGGGAT	84132
rs560840940	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6126172	ATAGTATGTAACCTT[G/T]TGGAATTGGCTTTTT	84132
rs560844077	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136160	CAGGCGTGTACCACT[A/G]TGCCAGGCTAATTTT	84132
rs560849559	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114417	CCAACTTTGACATTT[A/G]TCAACTTACGGGCAG	84132
rs560850740	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126154	CAGTGTTACGTGAAT[C/T]ATATAGTATGTAACC	84132
rs560858256	snp	A/G			intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153499	CTAATATTGGGCTTC[A/G]GCGAGATGTATTTAA	84132
rs560873521	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6099482	GCCTCCCAAAGTGCT[G/T]GGATTACAGGCGTGA	84132
rs560880058	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160531	TGCCTCCAACTCACT[A/C]ACCCTGCGCCTCTTG	84132
rs560898080	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6092015	TTCTTCTTCTTCTTC[C/T]TCTTCTTCTTCTTCT	84132
rs560913885	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131658	CAGTTGTTGGGGCTT[C/T]CAGGTTGCTGACTTT	84132
rs560961362	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6097833	CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC	84132
rs560989076	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6125383	TAATCTCAGCTACTT[C/T]GGAGACTGAGGTGGG	84132
rs560996762	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121478	CCTTTTTTTTTTCTT[A/G]TTTTGGCATTAGGGT	84132
rs561017788	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6124862	AGGTTATATCTTTAA[C/T]GTATCAGTTTACCTT	84132
rs561055046	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156642	TAGATAAGAATTGTG[C/T]GTGTCTGCACAGTGA	84132
rs561059743	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6142777	GTGGTTTAGCTGCTC[A/G]GGAGGCTGAGGTGAG	84132
rs561091227	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153188	TGGGTCAGGAGAATC[A/G]CTTGCACCCAGGAGA	84132
rs561095909	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6078860	CTTGGTATTCCTTAG[G/T]TCAACTAACATATTT	84132
rs561136435	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126509	CCAGGATGGTCTCTA[C/T]CTCCTGACCTCGTGA	84132
rs561243851	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147184	GGAGGCCTCAGGCCA[A/G]GTTGAGGGGTAGGAT	84132
rs561260616	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6152160	AGGACGGCCCCGTGG[C/T]GAGAGGCTGTGCAGG	84132
rs561316407	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120841	CACCTGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT	84132
rs561343076	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6108797	ATATTAAAAAAAAAA[A/T]TTTTTAAGGCCATTT	84132
rs561351382	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113923	ACTGTGCCCGACCCA[A/G]TCTCAGCCTTCTGTT	84132
rs561355324	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6108463	TTCATAGCATGGGTA[A/G]TACTTTTTTGTACTT	84132
rs561356232	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6084787	GCAGTGGCAGAATTT[C/T]AGCTCACTGCAACCT	84132
rs561358008	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6142335	GATTCTTCTGCCTCA[A/G]CCTCCCAAGTAGCTG	84132
rs561411266	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6090578	AAATTAGTTGGGCAC[A/G]GTTGTGCATGCCTGT	84132
rs561414529	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113613	CAGCCTTTTGGTTTT[C/T]TTTGTTTTTGTTTTT	84132
rs561459138	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110493	CAGATATTTGTGTTT[C/G]AGTTTGATATCAGTA	84132
rs561473507	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6109901	AGATGAGGTTTCACT[A/G]TGTTGGCCAGACTGG	84132
rs561480931	snp	A/G	1.72818e-05	0.00293949	missense	USP42	GRCh38.p7	7:6156977	CCTCTGGAAGGCGTC[A/G]GACCTTTCCGTGAGA	84132
rs561519405	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6119698	CCTTGTTTTTTGTTG[A/T]TGTTGTTGTTTTGTT	84132
rs561594097	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129880	AAAAAAAAAAAAGGT[G/T]TCTTTTATATACATT	84132
rs561595327	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115083	TCTCAAGTTTCTTTA[A/C]ATCTGTAACCCTCTC	84132
rs561605237	snp	A/C	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6138882	TTCCGTGAAACCAGT[A/C]CCTGGTGCCCAAACG	84132
rs561609826	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6142273	CCAGGCTAGAGTGCA[A/G]TGGCTCGATCTCGGC	84132
rs561609847	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104117	TCTCGCTCTGTCGCC[C/T]AGGCTGGAGGGCTGC	84132
rs561635020	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077411	GGCTTTCATCTTACT[C/G]TCTCCCTCTTTCATC	84132
rs561668453	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152229	AGCTCAGAGTGCGGC[C/T]GGATGTCACCATACT	84132
rs561669622	in-del	-/TTGTG	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6158355	CTGGACGCCCATTGT[-/TTGTG]TTCACGTGTGAAGCG	84132
rs561674242	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080823	TAACTGGATTCTTCA[A/G]TAACAGTAAATCTAG	84132
rs561746569	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081120	TTTAGGCTCCTAGGA[C/G]ACTTGATTCTGGCTG	84132
rs561841304	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6124411	TAGCTGGGACTACGG[A/G]TGCACCACCACACCC	84132
rs561852755	snp	A/C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155202	CGACTCCAGGTGAGC[A/C/T]TGGGGCCTTGTGCTC	84132
rs561856352	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6141056	CTGTAGTTCATTTAT[A/G]ATTTAGACTACTTGT	84132
rs561961547	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101110	CAGTGAAAGGAGTGG[A/G]GCAACAATATTGTCT	84132
rs561964669	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6135265	GTCCCATAATAACTC[G/T]TTGACATTGGGCAAA	84132
rs561979114	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6141486	CAGGCGTGAGCCACC[A/G]CGCCCGGCCTGAATT	84132
rs562000813	snp	C/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6155961	AGGATCTCACTATGC[C/T]GCGCACGCTGTTCTC	84132
rs562039807	snp	A/G/T			intron-variant	USP42	GRCh38.p7	7:6111664	CTGGAGTGCAGTGGC[A/G/T]CGATCTTGACTCACT	84132
rs562044029	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145022	ATTCCGCTATCCTCC[C/T]GGTTAACCATGCCCT	84132
rs562093167	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133709	ATTTTTAGTAGAGAT[A/G]GGGTTTTTCTGTGTT	84132
rs562093818	snp	G/T	2.76453e-05	0.00371778	missense	USP42	GRCh38.p7	7:6154682	CCGAGGGCGAGCGTG[G/T]CTGGGGCCGGGAGAA	84132
rs562094236	snp	C/T	0.00636936	0.0560724	intron-variant	USP42	GRCh38.p7	7:6088753	TCATCAAGGTGAGTT[C/T]GACATTTTGCTCTCC	84132
rs562096128	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6153693	TATTTGTCCTTGTAA[C/T]GCAATGACATGAGCC	84132
rs562098554	in-del	-/T	0.489837	0.0705577	intron-variant	USP42	GRCh38.p7	7:6102110	GGTAGTCTCCTAAGA[-/T]TTTTTTTTTTTTTTT	84132
rs562122665	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6119473	GAGATCTTACGTCAA[C/T]CAAAATAAAAAAGTT	84132
rs562128278	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6109335	TGTGAAGTCCAGACA[C/T]TAAGATGTTGTGCTG	84132
rs562197783	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6107705	TGAGCACCTGCGCCC[A/G]GCCTCTTCTTTCTTT	84132
rs562233559	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138680	CAGCAGGTGAGCATC[C/T]CCACCTGAGCTCCGC	84132
rs562296787	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157730	CTGATGCTCGGTACT[C/G]ATTTGCTCGCTTGGT	84132
rs562323372	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129112	CCACTGGGCCTGTAG[A/C]CTTTTTAGTGGTCAC	84132
rs562360820	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123479	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	84132
rs562382201	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134039	GGGACTACAGGTGCC[C/T]ACCACCACGCCCAGC	84132
rs562389083	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6082271	GTAGCTGGGACTACA[A/G]GTGCCCGCCACCAGG	84132
rs562408381	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6087396	GTTGTCCAGACTGGA[A/G]TGTGATCATAGCTCA	84132
rs562432149	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158221	TCCCACGCTGTCTGG[A/C]GGCTTCGCTGTCACT	84132
rs562439440	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087917	ATCTGCTTTGTAGTC[A/G]TGTTGCAAACAGTAA	84132
rs562447543	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120655	GTGGCACAATCTCGG[C/T]TCACTGCACCCTCTG	84132
rs562454609	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095059	TCCCAAAGTGCTGGC[A/T]TTATAGGTGTGAGCC	84132
rs562475051	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080962	TTTTAAACACATTAC[C/T]CTGTGTCTCAGTTTT	84132
rs562514857	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6159384	CACTTAACGCACACA[C/G]ACAGCAGAGGCCCTG	84132
rs562546356	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6110719	TATACTCAAATTGAA[A/G]ATGTAGTCAAATGTA	84132
rs562546400	snp	A/G/T	0.0002433	0.0110271	intron-variant	USP42	GRCh38.p7	7:6116762	TATGCCAGAATTAAC[A/G/T]TTCTGTTTGCCCTCA	84132
rs562556644	snp	C/T	0.0119091	0.0762411	intron-variant	USP42	GRCh38.p7	7:6087335	CGCACCTGGCCTAAG[C/T]GCTTCTTTTTTTTTT	84132
rs562607485	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116130	AAAAAAACGTCTGAT[A/G]CCAGCAACTTGGGAC	84132
rs562620187	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093179	CCCTTCCTTCCCTCC[C/T]TCTCTCCCTTCCTTC	84132
rs562630718	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6161118	GGAACTGTTCCAATC[A/C]ATCAATTTCCCAGTT	84132
rs562648462	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081388	AGATGGCGGGCGGCG[A/C]AGCCACAGCCCCGGC	84132
rs562663001	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112992	CACTGCAATCTCTGC[C/T]TGCTGGGTTCAAGCA	84132
rs562700227	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107123	AATGAAGGCGAATGG[A/G]TAGCTTTGGTTGGTT	84132
rs562769188	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132167	CTAGGCTCAAGCGAT[A/C]CACCCGCCTTGGCTT	84132
rs562806873	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6101280	CAGTGCCCACTGCAG[G/T]CTCCCTAAGTCTGGA	84132
rs562832921	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080165	GAGGCAGAGCTTGCA[A/G]TGAGCCAAGATCGCG	84132
rs562864890	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148162	GGGTACCAGGGTGAA[A/G]CCCCGTCTCCACAAA	84132
rs562879022	snp	C/T	3.35087e-05	0.00409307	synonymous-codon	USP42	GRCh38.p7	7:6156862	AAAATCAGAGGACTT[C/T]GTTAAAGATTCAGAA	84132
rs562892352	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6123028	TGGGGTTTCGCCCGT[G/T]TTGGCTAGGCTGGTC	84132
rs562899446	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6158612	CCCATGGAGTGCTGG[A/G]GAAACAGCCGGAGAT	84132
rs562904886	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097463	AGGCTGAAGTGTGCC[A/G]TTGCATGATCATAGC	84132
rs562964505	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106406	TAAATAGTGAAACTC[C/T]ACAAATGAAGAAAGA	84132
rs562964791	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6137831	GACTACAGGTGCTTG[C/T]CACTACCCCTGGCTA	84132
rs562969660	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153042	TTGGGAGGCTGAGGC[A/G]GGCGGATCACCTGAG	84132
rs563003626	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079834	AAATTTGTCATTCTT[A/C]CTCAAGTTTTAAAGA	84132
rs563008359	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6152527	AGTGCCCTCACTGAG[C/G]CCCTCTGTTAGGAGG	84132
rs563033480	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092579	TTACCTTCCTCATTT[C/G]AGGCATCATGACAAT	84132
rs563104082	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6135077	TGATAGGCATGAGCC[A/G]TGGCGCCTGGCTTCC	84132
rs563196258	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6143321	GGTGTGGCTGGGCAC[A/G]CACTGTCTGCCAAAT	84132
rs563219272	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091982	AGGACGTATTTTTTC[C/T]TCTTCTTCTTCTTCT	84132
rs563225077	snp	A/C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132738	GTGCAGCGTCGAGAT[A/C/G]TCGGCTCACTGCAAC	84132
rs563237147	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141596	TGGAGTCTTGCTCCA[G/T]TGCCCAGGCTGGAGT	84132
rs563252291	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153307	TGAAACAAAACAAAA[A/C]AAAAAAATAGAGGAA	84132
rs563276752	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103956	GGGCGTGGTAGCGCG[C/T]GTCCGTAGCCCCAGC	84132
rs563283214	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097773	TTTTTTGCATTTTTA[A/G]TAGAGGCGGGGTTTT	84132
rs563298759	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6136043	AGAGTCTTGCTCTGT[C/T]GCCTAGGCTGGAATG	84132
rs563317445	snp	A/G	7.67725e-05	0.00619519	missense	USP42	GRCh38.p7	7:6155068	GTGGAGAACAGTGAC[A/G]GTCATGTTGAAAAGA	84132
rs563320505	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104396	CAGACCTTGTTTCTA[A/G]GAAACAAAAAATAAA	84132
rs563336336	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6100991	CTGTCTTAAACCAGG[A/T]TATCTAGAAGTGAGG	84132
rs563349165	snp	C/T	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6119857	TACAGGCATGTGCTA[C/T]AACACCTAGCTAATT	84132
rs563403575	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6111993	TAATAACTTGTTAAC[C/G]AGTAGTTATTCTAGT	84132
rs563459258	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6134603	GAGGGGCTGTCCGGT[A/G]CATTCGAGGCTGTTG	84132
rs563463807	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6086233	TTTTTTGAGACAGAG[C/T]CTCGCTCTGTCGCCC	84132
rs563478754	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6155762	AAATTTGCTTCTGTA[-/T]TTTTTAAGAGACAGG	84132
rs563501674	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6084082	CCCAGGCTGGAGTGC[A/G]GTGGCTCAATCTCGG	84132
rs563536781	snp	A/G	0.00557542	0.0525036	intron-variant	USP42	GRCh38.p7	7:6126062	ATGTTTCCCTTTCCA[A/G]GCCCACTTGTGTCCC	84132
rs563586704	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6093004	GGAGCTGGAATTTAC[A/G]TCTAGTGTGTCTGTT	84132
rs563593360	snp	A/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6136411	TCTTTGATAACAAAT[A/T]TTTAGTAAAACATTT	84132
rs563651704	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6119996	TTTGAGACGGAGTCT[C/T]GCTCTGCCGCCCGGG	84132
rs563675259	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159393	CACACACACAGCAGA[A/G]GCCCTGGCGATTTTG	84132
rs563677543	snp	A/G	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6124812	ATCTGCTTCATTGGC[A/G]TATTTTTGATATTTT	84132
rs563696364	snp	A/G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6146747	TGATGAGTTTGCTCC[A/G/T]CATCGCACTCTGTGG	84132
rs563738241	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113514	TTTTGCTCTCCTTTC[C/T]CCACCAAGCTGTAGC	84132
rs563740134	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6113117	ACCATGCTGGCCAGG[C/G]TGGTTTCAAACTTAT	84132
rs563749897	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089800	CCTCCCAAAGTGCTG[C/G]GATTACAGGTGTGAG	84132
rs563750399	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119435	ATTATTGTGCAGGTA[C/T]GCTGCAGCCTGGGCA	84132
rs563811981	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6095906	TAACTGGGACCACAG[A/G]TGCCACCATACTTGG	84132
rs563817038	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129322	GCATTTTGGGAAGCC[A/G]AGGCAGGTGGATCAC	84132
rs563830417	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6078101	AGCCGAGATCGTGCC[A/T]TTGCACTCCAGCCTG	84132
rs563830917	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6136366	CGTCATGTATTAGAA[A/C]ACAAATACATTTTGT	84132
rs563859906	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115002	GCCCTATATATATAT[A/T]TTTTTAAGCAGTTGT	84132
rs563893341	snp	A/C	0.000156902	0.00885588	intron-variant	USP42	GRCh38.p7	7:6150327	CGTCAGGGTCTTCAG[A/C]CTCGTTTGTGGCGGT	84132
rs563934308	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6133187	ATATTAATATAGACT[C/T]ATGTGAACTGACAGC	84132
rs563969913	snp	C/G	3.43938e-05	0.00414677	intron-variant	USP42	GRCh38.p7	7:6141006	TTCATAATTATGGGA[C/G]TAATTACATTTTTAA	84132
rs563971534	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134254	TAGGAATATATTTGT[A/G]ATATCCTTTTTAAAG	84132
rs564001836	snp	A/G	0.000798403	0.0199641	splice-donor-variant	USP42	GRCh38.p7	7:6078764	GAAGGCACTTGTCAG[A/G]TGAGCACAACTACTT	84132
rs564014045	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime	USP42	GRCh38.p7	7:6084648	TCGCCATCGCACCTG[A/G]CTGTTTGTTGCAGAT	84132
rs564072131	snp	C/T	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6120965	TTTATTGCTAGCATA[C/T]AGAAATACATTTTTC	84132
rs564075231	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6145126	ATCACGAGGTCAGGC[A/G]TTCAAGACCAGCCTA	84132
rs564092674	in-del	-/A			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080379	ATAAGCATATACCAC[-/A]AAAAAAACAGTATTG	84132
rs564097746	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6151586	GGGACTACAGGCATG[C/T]GCCACCCCACCCAGC	84132
rs564107888	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107900	GTTCATTGAAATTGA[C/G]AAACATCTTTTCTAT	84132
rs564129685	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6078324	ATAGCCTAAGCCATC[C/T]GGGCACGATGGCTTA	84132
rs564136790	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6122455	CATGCCTTTTGTTTT[A/G]TTTTGTTTTTTTGTT	84132
rs564140765	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6102025	TTGCAGTGAGCCGAG[A/G]CTGTTCTAGGAGACA	84132
rs564166409	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103467	GGTTGCAGTGAGCCG[A/C]GATGACACCATTGCA	84132
rs564180880	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123709	AAAAATTAGCTAGGC[A/G]TGGTGGTGTTCTTCT	84132
rs564196994	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6082931	TTAAATTAAATATAT[A/G]TAGATACATATATAT	84132
rs564202672	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158558	GAGTGTGTGAGAGAG[A/C]GCTGGGGGTTGCGGG	84132
rs564225391	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6095309	GTTAACTTGGACTCT[A/G]TAAGCAAAAGCCTGG	84132
rs564248998	snp	A/C	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6108363	GGCAACGTAGTGAGA[A/C]CCTGTCTCTACAAAA	84132
rs564428940	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6149216	AGGCGAGGGTGATTC[C/T]TCCTTCCTGGCACTC	84132
rs564441243	in-del	-/C	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6101441	CAGGTTAAGTAATTT[-/C]TGTAGGTCACAGAGC	84132
rs564442653	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6128058	CTCAAGCTATCCTCC[C/T]GCCTCAGCCTTCCTG	84132
rs564477364	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093983	CAACCTCCACCTCCC[A/G]GGTTGAAGTGATTCT	84132
rs564501197	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138617	CTGGGCCGTAGACTG[G/T]TACCCAATGTGGCCT	84132
rs564565799	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137977	AGCCACCACGCCCGA[A/C]CACATATATTTATTT	84132
rs564630018	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106535	CACTTGTGAAGTCTC[A/G]TTCCTCCACACAGAT	84132
rs564642842	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6158166	ATGTGAAATTCAGAC[C/T]TCAGTGTCTGTGGCT	84132
rs564669317	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081582	AGCCCGCCGCAGACC[A/C]CGCCCCTTCTCCTTT	84132
rs564671815	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6083963	TGATTAAGGGTACCT[A/G]ACTCCCAAGCTGGTT	84132
rs564695754	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6161015	CTGTTTTCTGTAATG[C/T]CTGATACTAGAAACT	84132
rs564712192	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126896	ATGCCCAGGACTGCA[A/G]ATGCTGGGTTATATG	84132
rs564759139	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6085733	GATTCTCCTGCCTCA[C/G]CTTCCTGAGTATCTG	84132
rs564763464	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6093231	CCTTCCTCCCTCCCT[C/G]CCTCTCTTCCTCCTT	84132
rs564777546	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088157	ATTTAAAAACTAGCC[A/G]GGTACTGAGCTATGA	84132
rs564787258	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133309	GTCCTTTTACCTTCA[C/G]ACTCTAATGATGTAT	84132
rs564827498	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080885	CAACATTTCAAACAT[A/C]TGGAAAAGTATCATC	84132
rs564842666	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6108960	GAAAGCTTTCTCTAC[A/G]CCAGGTCAGAGGATG	84132
rs564848737	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161994	TATTTACCGCAAATA[G/T]AAATATTTTCTAAGA	84132
rs564875578	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137619	CGTCTTGGCCTCCCA[A/G]AGTGCAGAGATTACA	84132
rs564880919	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6117344	CACTCAGCATAATCC[C/T]GTCAACATTATTCCA	84132
rs564890432	in-del	-/A			utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161934	ACATCATTGAATAAC[-/A]GACACTCCAGAAATC	84132
rs564941774	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6126582	GAGCCACTGTGCCGG[C/T]CTGATAACGCCACAG	84132
rs564953354	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132143	TTTGGCCAGGCTGGT[C/G]TCGAACTCCTAGGCT	84132
rs565039558	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087277	CTCAGGTGATCTGCC[C/T]GCCTTGGCCTACCAA	84132
rs565089183	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117644	GAAGGGATTGCAGTG[C/T]TTTATAGTCCCACCA	84132
rs565145644	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115228	GTCATGAGATTTCGG[A/G]TCTTGTAAAGATTGA	84132
rs565149228	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6122431	GCTGAGACTACAGAC[A/G]TGCACCACCATGCCT	84132
rs565166844	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136572	TTTGCTCTGAAACTT[A/G]GATTTCTATGCTGAG	84132
rs565169633	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143252	ATTATTGGGCAGATT[C/G]GGTGGGAGGAGAGAG	84132
rs565228985	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152194	TGCTTGCATCTCTGC[A/G]CAGGTTGGCTGTGAG	84132
rs565230080	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142856	GCCACTGCACTCCAG[C/T]CTGGGTGGCAGGGCA	84132
rs565230341	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6093839	CTATAAGAGTTAAAA[A/G]ACCTTGTTCATGTTT	84132
rs565240538	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6152504	CAGAATGGCCCCCGG[C/T]GGGTGGGAGTGCCCT	84132
rs565278606	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6141035	AAAATAAGTCATTTT[A/G]TGTAACTGTAGTTCA	84132
rs565290857	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6149256	GAGCTCCCAGGAAAC[C/G]CAACCAGGTAGCAAG	84132
rs565306027	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079815	TGAGACACCATGCTT[C/G]GTGAAATTTGTCATT	84132
rs565352186	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6147164	AAGCACAGATGATGA[A/T]CAGAGGAGGCCTCAG	84132
rs565369145	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6079328	CCCGGCGGGGTGGCA[C/G]GTGCCTGTAATCCCA	84132
rs565431100	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098010	CCCTGGTTTAAGCGA[G/T]TCTCCTGCCTCAGCC	84132
rs565433063	snp	C/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6105901	GTCACTTGTTTATGG[C/G]AAAACATGTTGGTTA	84132
rs565465341	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6102346	CTCGAACTCCTGATC[C/T]TGTGATCTGCCCGCC	84132
rs565489027	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114634	ATAAAATACGTGTGT[A/G]TGTATATATGTATGT	84132
rs565490826	snp	A/G	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6089602	CAAGGGTGCGATCTC[A/G]GCTCACTGCAACCTT	84132
rs565525364	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120583	GGGATTTCAGGCATG[A/C]GCCACTATGCCTGGC	84132
rs565539342	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6143575	CTTTGTGGTCAGGTA[A/G]TAGAAGTAATTTTTT	84132
rs565567237	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129430	GGCATGGTGGCGGGC[A/G]CCTGTAATCCCAGCT	84132
rs565588354	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6120046	TCTCGGCTCACTGCA[A/G]CCTACGCCCCCGGGT	84132
rs565598888	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124577	CTTTAAAGTGGATTT[A/C]TTATAAATAGCTTAT	84132
rs565629453	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134340	TTCTCCTTGTTACCG[G/T]TCATTTCTGCATCTT	84132
rs565665287	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158764	GGCTGCTTGGTACCC[A/G]AGGATCCGAGGATGC	84132
rs565701042	snp	A/G	0.0178098	0.0926698	intron-variant	USP42	GRCh38.p7	7:6082351	GCCAGGATGGTCTCG[A/G]TCTCCTGACCTCGTG	84132
rs565703614	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134817	TTGAGACAGGGTCTC[A/G]CTCTGTTGCCCAGGC	84132
rs565724891	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114351	TTATTTTTTAAATGT[C/T]CAAAGTGGATATAAA	84132
rs565811555	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081731	CGCTGCTGAAAGCCG[A/C]CTGCGCCTACGTGGA	84132
rs565842774	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6078264	TTACATTGCAATAAT[A/T]AATACATGTTAAACT	84132
rs565850290	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155655	CACACTTTTCCTGTG[C/T]CTGCCCGCCTGCCCA	84132
rs565882713	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6157929	CCCACTTCCTCTCCC[A/G]TTGGTGTCCGGTGAC	84132
rs565905092	snp	A/G	0.000897464	0.0211643	missense	USP42	GRCh38.p7	7:6154454	GCGGGGAGCCCGCCA[A/G]AGAGAGCAGGAGCAA	84132
rs565921096	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119109	AGTCCTAGTTACTTC[A/G]GAGGCTGAGGCAGGA	84132
rs565936360	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6108015	CATAGTGAAACCCGG[C/T]TCCACTAAAAATACA	84132
rs565986868	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129908	ATTTAGAACCATATC[A/G]GACAATGTTATAATT	84132
rs566002269	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6094809	CTTGTTCCACTTGGC[-/T]TTTTTTTTTTTTTGG	84132
rs566009009	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089879	GTGTCTGATGAAATA[C/T]GGCTTGCTGTGGCTG	84132
rs566025749	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159134	ACTTCGGCCCCTTGT[C/T]TTTCTCTTTCAAACT	84132
rs566079655	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6110865	TAGGGGGCATGAAAT[G/T]AAAATGAGAAGTTCT	84132
rs566128361	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123501	ACCCCGTCTCTACTA[A/C]AAATACAAATATTAG	84132
rs566226236	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6086046	CTCTTTTTTTTTTTC[-/T]TTTTTTTTTGAGACA	84132
rs566273054	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113660	GAAGTCTCTCTCTGT[C/T]GCCCAGGCTGGAGAG	84132
rs566274212	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148424	AGCCTGGGTGTCAGC[A/G]CCTTTAAATTTTAGG	84132
rs566295240	snp	C/T			missense	USP42	GRCh38.p7	7:6153923	CTACCAAAGAAGGCG[C/T]CTGGGAGGCCATGGC	84132
rs566353883	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112216	CACTTTGGGAGGCCA[A/T]GGCAGGTGGATCACC	84132
rs566405738	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151823	ACTGGCAGTGCAGTG[A/G]GTTTGTTTACACCAG	84132
rs566421582	in-del	-/C	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6102235	ATTCTCCTGCCTCAG[-/C]CTCCCAGTAGCTGGG	84132
rs566435442	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6144826	AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG	84132
rs566466828	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6106751	TTTTTTTTTTCTTAA[A/G]GAGACAGGGTCTCAC	84132
rs566475833	snp	A/C/G	0.0113671	0.0745273	missense	USP42	GRCh38.p7	7:6153826	GGCAGCCCCGCCGCC[A/C/G]AATCCCTGGAGGAGC	84132
rs566502823	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094123	TCCTGACCTCGTGAT[C/G]CACCTGCCTCAGCCT	84132
rs566599644	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6099300	GCTCATTGCAACCTA[-/G]GCCTCCCAGGTTCAA	84132
rs566602666	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6124727	TTTTTCCTATTTGTC[C/T]CATTTATTCTTGGTT	84132
rs566620168	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6096220	GCTCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG	84132
rs566654903	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6105665	GCGGCCACCCCGAAG[A/G]GAGAGGAGAAGCCGG	84132
rs566688713	snp	C/T	0.0126979	0.078662	intron-variant	USP42	GRCh38.p7	7:6100557	CTTGTCTCGAACTCC[C/T]GACCTCAGGTTATCT	84132
rs566714128	in-del	-/A	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6118234	CTCATCTCTATATAT[-/A]AAAAAAAATCAAAAA	84132
rs566755509	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6132966	GTGAGCCACTGCGCC[C/T]GGCCCAGCACTGTTT	84132
rs566767719	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138276	TTAAAAAATAATTTG[A/G]TCTTTTAGCTGTTTA	84132
rs566772542	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122199	CTTTCTTCTTTTCCA[A/G]TGTAAGTGTCAAATG	84132
rs566785010	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126662	GGGATATCGTGAGTG[A/G]AGCTGCGGTAAACAC	84132
rs566786152	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137356	ACACATGCATGCATG[C/T]ATTCATTCATCCATT	84132
rs566801648	snp	A/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6099693	ACCATCCGGGCACAG[A/T]GGCTCATGCCTGTAA	84132
rs566801836	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6107189	CTTGAATTGTGCTTT[C/G]GTTAAATTTTTTTTC	84132
rs566854995	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160365	GGGCCCAGCAGATGG[C/T]GCCTCCCTGGCTGAG	84132
rs566876402	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098139	TGATCTTCTGAACTC[A/G]TGATCCTTCCACCTT	84132
rs566890568	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131845	ACTTGGCAGGAGGAA[C/T]AGAAAACTACCTCTA	84132
rs566909615	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086457	TGATCCGCCCACCTC[A/G]GCCTCCCAAAATGCT	84132
rs566920124	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157577	TAAATTTTGTGTTTT[A/T]AGTAGAGACGGTGTT	84132
rs566927212	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159891	GAGCCTTGCTCCCTC[A/G]TCCGTCCCGTCCCCT	84132
rs566930220	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6098658	CCCGGTTCAAACGAT[G/T]CTCCTGCCTCAGCCT	84132
rs566950722	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6136718	ATTAGGCTACTCTGG[A/G]CACACTGCCTGTGGA	84132
rs566997662	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6110390	CAGTTGATGCAATGC[C/T]CAGTACATAGAAAAT	84132
rs567036100	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080542	AGCAGTTGGAGACCA[G/T]TCTGGCCAACATAGT	84132
rs567060986	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6144685	GACCACTCTGGCGAA[C/T]GTGGCAAAGCCCTGT	84132
rs567063970	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159557	GGGACGCAGGCAGAG[A/G]AGTTTTAATTCTGCG	84132
rs567093904	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092763	GCTGGGTCTAAGACC[C/T]GGCCAGCCACAGTCT	84132
rs567112012	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6079229	TTTGGGAGGCCAAGG[C/T]GGGCGGATCACAAGG	84132
rs567148266	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6086951	CAGGCTTGTCTCGAA[C/T]TCCTGACTTCGGGTG	84132
rs567156125	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155785	GAGACAGGGTGTTGC[G/T]CTGTCACCCAGGCTG	84132
rs567170791	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6091712	ACACACACACACACA[C/T]ACATATATATGTTGC	84132
rs567216778	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	USP42	GRCh38.p7	7:6160687	GAGAACTTTTTTTTT[A/G]GTTTTTACCTTTTCT	84132
rs567223014	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6156190	TTACCAAAAGCCATA[A/T]GGAAAATAGGCAGTG	84132
rs567225751	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131762	AGGTCCGTAGCATGT[C/T]TCTTTCTCTTTCTAC	84132
rs567235500	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121090	TGTGATACGTGAATA[A/C]AGATAATTTTACTTC	84132
rs567271395	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6089055	TATTTATTTATATTT[A/G]TCTTTTTGAAATGGA	84132
rs567293638	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6146399	GCATGGTGCCTCACG[C/G]CTATAATCCTAGCAC	84132
rs567314889	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125646	TTTTGTTTTAGATAG[C/T]TTAAAGCTTTTAAGA	84132
rs567326703	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6125100	GCAGGAGAATCGCTT[A/G]ATCCCGGGAGTTGGA	84132
rs567356075	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116149	GCAACTTGGGACAGG[C/T]GAGGTTAAGAAATCC	84132
rs567387913	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130501	ACTGGGTGGGTGGAA[A/T]TCTGGGCTCCCCACA	84132
rs567393432	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6129517	AGCCAAGATTGTGCT[A/G]CTGCACTCCAGGCTG	84132
rs567404861	in-del	-/TG	0.0126979	0.078662	intron-variant	USP42	GRCh38.p7	7:6119689	CATTTAGGCCTTGTT[-/TG]TTTTGTTGTTGTTGT	84132
rs567437091	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142511	GTGAGCCACCACGCC[C/T]GCCCGGAAAATTTTC	84132
rs567439071	snp	A/G	6.62965e-05	0.00575707	synonymous-codon	USP42	GRCh38.p7	7:6147850	CAACAAACAGGCTGC[A/G]CCAGGCTTTATCGGA	84132
rs567440060	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152549	GTTAGGAGGGCGTAG[A/G]TATTAAACCGGAATG	84132
rs567467273	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6150756	CCTCCTGCGTGGCCA[C/T]CTCTCTCTGGTTAGC	84132
rs567522278	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6115686	AGGATTGGGATTCAG[A/G]TTGCATGAAAAACAT	84132
rs567658032	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109060	AATCAGCACAGGGTG[C/T]TGTGGGGGCCTTGAG	84132
rs567665502	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6157378	CTCTTGGTTTGGTTT[G/T]GTTTTATTTTATTTT	84132
rs567672051	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6100255	CCAGCCCTAACTAGT[A/C]CCCCTAGATGGGCGC	84132
rs567719691	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120016	TGCCGCCCGGGCTGG[A/C]GTGCAGTGGCGCTGT	84132
rs567732380	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113725	CTCCCGGGTTCACAC[C/G]ATTCTCCTGCCTCAG	84132
rs567735614	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6078189	GAACCATTAAGCCAC[C/G]CTGCTCTGATCCGTG	84132
rs567753807	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133859	TCTTCATGTGTATAA[A/G]CAGATTTGCATCTAT	84132
rs567779846	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096363	CAGTAGGGTTTTATG[A/G]GGTGATGGAGAGGGG	84132
rs567799081	in-del	-/G	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6145959	CCAGTAATCCCAGCA[-/G]CTCCGGAGGCTGAGG	84132
rs567809075	snp	C/G	0.00478085	0.0486577	intron-variant	USP42	GRCh38.p7	7:6084218	TTTTAGTAGAGACAG[C/G]GTTTCACCATGTTGA	84132
rs567836935	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6118091	TTTTATTCGTTGTGC[C/T]GTAGGTGTTTTAAGA	84132
rs567844391	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096977	CATCCATGCTGGAGT[A/G]CTGTGGCATGATCTT	84132
rs567847472	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6094463	GGCATGAGCCACTAA[A/G]CCCAGCCTGAGAGAT	84132
rs567872505	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6141332	CTCAGCCTCCCGAGT[A/G]GGTGGGACTATAGGT	84132
rs567895105	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103397	AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCATCT	84132
rs567914147	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6146687	CCAAAAACCATCAAC[A/T]CTGCCATGTGCCTGG	84132
rs567928546	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6109354	GATGTTGTGCTGTGG[A/G]CAGTTGGGCCACTCC	84132
rs567967992	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120124	TGCCTGCCACCACGC[C/T]GGCTAATTTTTTTGT	84132
rs567972339	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6129391	CGAAACCCCATCTCT[A/T]CTAAAAATACAAAAG	84132
rs568015665	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6117590	TGGTCCTGGGGTGGG[A/T]GTGTACTTTAACATT	84132
rs568034990	snp	A/T	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6128906	GCTCACTACAGCCTC[A/T]GTCTCCCAACCTCAA	84132
rs568072884	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145215	GCGCACCTGTAATCC[C/T]GGCTACTCGGGAGGC	84132
rs568075651	snp	C/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6088277	TTTTTCTTTTTGCGA[C/T]GGAGTCTTGATCTGT	84132
rs568082295	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6140429	TGCTTCCATTTGTCT[C/T]TTCGTATTAGCAGTC	84132
rs568102121	snp	A/C	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6123183	AATGACCCTCTTCAT[A/C]CCAAATAATATTCTT	84132
rs568128476	snp	C/T	0.0643442	0.167427	synonymous-codon	USP42	GRCh38.p7	7:6154854	CCACAACCGGGGCCG[C/T]AGGGGCTGCGAGCCG	84132
rs568133576	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087665	CTCTCTTTCATTATA[C/T]GAAGTTGAGATATTT	84132
rs568143915	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119779	CACAGTCAGAGCTCA[C/T]TGCAGCCTTGACCTC	84132
rs568164673	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158714	AATTGGTTTTGCGTT[C/G]CCATTTCAGCGAATC	84132
rs568209705	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124074	AGTGATGGGGTTTCA[C/G]CATGTTGGCCAGGCT	84132
rs568222646	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083677	TGAGATATGTATATA[C/T]ACACACACACACACA	84132
rs568241595	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6112934	TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCCATT	84132
rs568247794	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093370	AGCTCACTGCAACCT[C/G]CACCTCCCGAGTTCA	84132
rs568249327	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6106012	GTTCTCGTTTTGGTG[A/G]CCTCTCAAAACGTTT	84132
rs568286219	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6125378	GCCTGTAATCTCAGC[G/T]ACTTCGGAGACTGAG	84132
rs568294800	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6113141	AACTTATAATCCACC[C/T]GCCTCGGCCTCCCAG	84132
rs568297208	snp	C/T	0.00318978	0.0398085	intron-variant	USP42	GRCh38.p7	7:6107524	AAGGGATTCTCCTGC[C/T]TCAGCCTCCCGAGTA	84132
rs568359206	snp	A/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6112861	CCTGGCTTCGAGTAG[A/T]TTGATCGCCATGTTG	84132
rs568379987	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6146970	CCAAGGCCAGCACCC[A/G]CACCCAGCTCTGTCC	84132
rs568401222	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6123533	CAGGCGAGGTGGCGG[A/G]CGCCTGTAGTCCCAG	84132
rs568404326	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081132	GGAGACTTGATTCTG[A/G]CTGACGTGCTGCGAC	84132
rs568411865	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6153599	GTAACTAACCTGCAC[A/G]TTGTGCACATGTAGC	84132
rs568445683	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157669	ACTTTTGCAGCGTAT[A/G]CGTTACTCTCCCGAA	84132
rs568504690	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084263	AACTCTTGACCTCAG[A/G]AGATCTGCCCACCTT	84132
rs568525373	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127320	TGGTCAGCCTTTAGT[A/G]GATTGTGCTTTTAGT	84132
rs568569086	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6107956	GATTGTATTTTTTTG[G/T]GTGATAATCTTACCC	84132
rs568612515	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144945	AAGAATTCACTTAAT[A/G]TAGATCCTGACTTGT	84132
rs568638731	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152731	CAGCTTTCATTATTA[A/T]CCCCGAGGATATATC	84132
rs568642511	snp	A/G	3.93321e-05	0.00443447	synonymous-codon	USP42	GRCh38.p7	7:6150056	TGACGAGGAGTCAAA[A/G]GGGCTGGGCAAGGAG	84132
rs568703294	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081648	ACGCGGGAGCACCCA[C/T]GGCGCATGCTCTCTG	84132
rs568726454	snp	A/C/G/T	8.56788e-05	0.00654462	synonymous-codon, missense	USP42	GRCh38.p7	7:6154380	AGCGAAGGAGAAAAT[A/C/G/T]GGCAGCCTCAGAAAG	84132
rs568826717	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6094042	CGTGCCACCACACCC[A/G]GCTAATTTTTTTTGT	84132
rs568843073	snp	A/C	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080516	CCAAGGTGGGTGGAT[A/C]ATTTGAGGTCAGCAG	84132
rs568849895	snp	A/G	0.0023933	0.0345097	intron-variant	USP42	GRCh38.p7	7:6111581	TTTAGTTGCTAGAAT[A/G]TTATTAGTTTCTTTT	84132
rs568875898	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6126616	CTTTAACTACTTTTC[C/T]ATTAAAGGATATCCG	84132
rs568935613	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6092216	AGATTCTCGCTTTGT[C/T]GCCCAGGCTGGAGTG	84132
rs568954294	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6099601	GATCCACCTGCCTCA[G/T]CCTCCCAGAGTGTTA	84132
rs568966726	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106690	CCACCTCAGCCTCCT[A/G]AGTAGGTAGGACTAC	84132
rs568978320	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079995	TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAGGT	84132
rs568993207	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138083	GTGTGTGTATCCACT[A/G]ATACACACATGGTTC	84132
rs569005876	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120662	AATCTCGGCTCACTG[C/T]ACCCTCTGCCTTCTG	84132
rs569042096	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099060	ATTCAACCTTTTCTA[A/T]TGTTCTGCTCCTTTT	84132
rs569045757	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158994	ACTGCACCGATGACA[A/G]GGTTTGCAGCTGGCG	84132
rs569105015	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106237	AGTATAATTAAGACG[A/C]AGGTTTTGTCTTTTT	84132
rs569120416	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094290	GCGATCCTCCCACCT[C/T]AGCCTCCTTAGTAGC	84132
rs569139544	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112114	TGTTTTTGTTTTTTT[C/T]CTGGCAGTTAAAAAT	84132
rs569146000	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143535	TTTAAGAAAGCTCTT[C/T]TGTATGTTTTTAAGT	84132
rs569211339	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6098955	AGCTTGAAGTTCTAC[A/G]GACATTAGAGTCCTG	84132
rs569211627	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131433	GAGCCGTGATCCCGC[C/T]ACTGCACTCCAGCCT	84132
rs569218549	snp	C/T			utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081765	CGGGTTCGCTCCGGG[C/T]CGCTCCTCCCTGCTG	84132
rs569233554	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097676	GCTCACTGCAAACTC[C/T]GCCTTCCGGGATCAT	84132
rs569263285	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141752	TTCCTAATTTTTTTG[C/T]TGTTTTTGAGCTTGC	84132
rs569268277	in-del	-/CCTCAGTCTCCCAA	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6128902	CTCAGCTCACTACAG[-/CCTCAGTCTCCCAA]CCTCAAATGATCCTC	84132
rs569270367	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6090911	ACTTAACTAAAAAGT[A/G]TTATGTATTTATCCT	84132
rs569289535	snp	A/G	0.00438332	0.0466095	intron-variant	USP42	GRCh38.p7	7:6142437	TAGCCAGGATGGTCT[A/G]GATCTCCTGACCTCA	84132
rs569308787	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6124962	GAGGTGGGCAGATCA[C/G]TTGTGGTCAGGAATT	84132
rs569310818	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142479	CCTTGGCCTCCCAAC[A/G]TGCTGGGATTACAGG	84132
rs569312315	snp	C/T			synonymous-codon	USP42	GRCh38.p7	7:6147862	TGCGCCAGGCTTTAT[C/T]GGACCACAGCTTCCC	84132
rs569316048	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6160645	GCGTGGTGCTTCTTT[A/C]GTAAATACTGTACAG	84132
rs569332386	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096749	TACTGTGCTTTTGTT[C/G]ACAGCCTGTCTTGCC	84132
rs569334027	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6089911	GCGCAGGAGGCGCCA[A/G]TGTGGCTTGAACCCG	84132
rs569371637	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147385	GGAGGGCAAGGCCAC[A/G]GTGAGCAATGGCTGT	84132
rs569410357	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6079002	ATAGATGTTACTAAG[C/G]GTTTTTTGTTTGTAA	84132
rs569415303	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6076907	TGATACAGAGTCTTG[C/T]TCTGTTGCCCAGGCT	84132
rs569434808	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160329	TGGAGGTGGAGGAGG[C/G]ATCTGGGGCGGGTGG	84132
rs569493040	snp	C/T	4.98666e-05	0.00499308	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115302	GCTTGGTTTCTGACT[C/T]TTTCTTGTTTATTTT	84132
rs569497637	snp	C/T	0.0162398	0.0886349	intron-variant	USP42	GRCh38.p7	7:6092143	TTCTTCTTCTTCTTC[C/T]TCTTCCTCTTCTTCT	84132
rs569498398	snp	C/T	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6109687	GGGTGTGAGCCACTG[C/T]GCCCCGCCCGGCCTT	84132
rs569505192	in-del	-/TAGT			upstream-variant-2KB	USP42	GRCh38.p7	7:6078238	AGAAATGTTTCTGGG[-/TAGT]TAATTTGTTACATTG	84132
rs569509244	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084403	ATTTTGTCTTGCTAA[C/T]GCTGATGTTTTCATT	84132
rs569514301	in-del	-/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6115720	GCACCTAATTAGACC[-/T]GTGAAGGTATTTAAA	84132
rs569555504	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114836	GCTAGGACTACAGGT[G/T]CCCGTCACCGCGCCT	84132
rs569581022	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124613	TGATCTTGCTTTTTA[C/T]CCAATAGTAGCCTCT	84132
rs569608041	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6091890	CAGCACTCTCAATCG[A/G]CATTTCTTCCTGAAA	84132
rs569609241	snp	A/G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6141078	ACTACTTGTTAGAGA[A/G/T]TATAAATTGAAAAAT	84132
rs569648273	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6144018	AATAGTAACAAGAAA[A/G]ACCAAAATACCACAA	84132
rs569666661	snp	A/C	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6150646	TGAATTATAATGTAT[A/C]GGATTTATTAACTTG	84132
rs569725760	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146901	CCTCTGAGCACCTGG[C/T]GTGGTCACAGCCAGC	84132
rs569731827	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6088324	GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACCT	84132
rs569759862	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130081	GCTCCCACCTCCTGG[A/G]CTCAAGCAGTCCTCT	84132
rs569864999	snp	C/T	0.00466282	0.048059	missense	USP42	GRCh38.p7	7:6154522	CCCCGGGAGCGCGAC[C/T]GCCAGGACCGCCACG	84132
rs569898252	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6086371	CCACCATGCCTGGCT[A/G]ATTTTTTGTATTTTT	84132
rs569911563	in-del	-/A	0.278399	0.248382	intron-variant	USP42	GRCh38.p7	7:6144869	GTCAGATTCTGTCTC[-/A]AAAAAAAAAAAAATT	84132
rs569915879	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079109	TTACAGTAATCAACA[C/T]TGAATACATTTATAA	84132
rs569992777	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155729	TGTCTCCATTTTTCA[A/C]CTTGAAATCCAATTG	84132
rs570042149	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113714	GCAACCTCCGCCTCC[C/T]GGGTTCACACCATTC	84132
rs570104326	snp	G/T	0.00398564	0.0444627	intron-variant	USP42	GRCh38.p7	7:6119713	TTGTTGTTGTTTTGT[G/T]TTTTTTTAGTGACAT	84132
rs570116074	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119235	AAAAGTTTTGGAACC[A/G]GGTAAGTCCTCCAAC	84132
rs570164867	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6102500	GGTGTGGTGGCTCAT[A/G]CCTGTAATCCCAGCA	84132
rs570181024	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6158658	CACTGCCGGTGAGGA[C/T]GGGTTGCCTGCGGGC	84132
rs570203111	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089493	CTTCCACCCAGAACA[C/G]TCTTCTGACCCTGGA	84132
rs570228138	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103340	TCAGGAGTTCGAGAC[A/C]AGCCTGACCAACATG	84132
rs570288821	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6157080	GATACTTGGAATTAG[A/G]AAGATAGAAACTATT	84132
rs570305082	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146274	GAAAACAAATTGCCA[C/G]ATTTTCTGGTATGTC	84132
rs570342243	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6140510	TTCCATTTATTTTAG[C/T]CCCCTATCGATGGGA	84132
rs570384412	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6105820	TTTTCCCATCTAGGA[C/T]TTTAACCCCTCTCAC	84132
rs570389591	in-del	-/A	0.377385	0.215112	intron-variant	USP42	GRCh38.p7	7:6145330	GTGGCACGCCATCTC[-/A]AAAAAAAAAAAAAAG	84132
rs570398628	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6132287	GCCTGTGCTGTGCCT[G/T]ATAAGAAGTCTGTTG	84132
rs570400853	snp	A/G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133810	CAGGCGTAAGCCACC[A/G/T]CACCTGGTGCATTTT	84132
rs570413667	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133458	TCAAGTTCACTAATC[C/T]TTTCTTCTGTGGTGT	84132
rs570415099	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6112785	GTTAGTGTATTTTAC[A/G]TGTGGCCCAAGACAA	84132
rs570465984	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6093252	CTTCCTCCTTCCTTT[C/T]TTCCTTTCTTCCCTC	84132
rs570493911	snp	A/C	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6149414	CCTGTGGAAAGTATG[A/C]GCGGGTAGGAGGGAT	84132
rs570506351	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089038	ATATTTATTTATTTA[C/T]TTATTTATTTATATT	84132
rs570568051	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6144497	TTTTCCCATTTTCTT[C/T]CCACTTTCTGAAGAT	84132
rs570648748	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088494	AACTCCTGAGTTCAG[A/G]TGATCACCCGCCTTG	84132
rs570678346	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6144744	GTGTGGTGGCAGGCA[C/G]TTGTAATCCTAGCTA	84132
rs570682338	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094828	TTTTTTTTTTGGTCA[C/T]CCAGGCTGGAGTACA	84132
rs570689079	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6116521	CAGATTCATGTGTGT[A/G]TGTTCTGGGGCTATT	84132
rs570741606	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161409	TGTATTTAATACAGT[C/T]TGTATCTGAATAATC	84132
rs570748755	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117959	CTTAGAGAGTTCTTT[A/G]TATATCCTCGATATA	84132
rs570777249	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6087100	GCAGTGGTGCGATCT[C/T]AGCCCACTGCAACCT	84132
rs570786580	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6132863	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	84132
rs570794019	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6141907	TATTGTTCACTTTTT[A/G]TATAAATGAGATTGT	84132
rs570795989	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6094177	ATGAGCCACCATGCC[C/T]GGCCTGTTGTTTTTA	84132
rs570846912	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6160801	TAATGCCCTGGAATA[C/G]AACATCTCAAATGCT	84132
rs570847217	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157229	CCCTGCAGTGTGGTT[C/G]CGTTGCACAGTTAAG	84132
rs570850942	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126669	CGTGAGTGGAGCTGC[A/G]GTAAACACATCTAGG	84132
rs570861987	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6102572	TCACAACCAACCTGG[G/T]CAACATAGCGAGCCC	84132
rs570878010	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079973	TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	84132
rs570893173	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6105603	CCTCCCCAGGCCTAG[A/C]CACCTGGCTGCTCCG	84132
rs570958376	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6122870	CTGCTGGCGCCCAGG[C/G]TAGAGTGCAGTGGTA	84132
rs570990511	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079414	AGTGAGCCGAGATTG[C/G]GCCACTGCACTCTAG	84132
rs571001514	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112316	TAGCTGGGCATGGTG[A/G]TGTGTGCCTATAATC	84132
rs571035907	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081080	AGTCTTGTACCTAAT[A/G]CCATTATTTGCTCTG	84132
rs571056376	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6156305	GTAACTACTGGTTTC[A/G]GGAAAAGTTAGCAGA	84132
rs571058266	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6160240	TTAATTAACAGGCTT[C/T]ATCAATGTGTCCTCA	84132
rs571071275	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127275	TGGTTGTTTTACAGA[C/T]AGAGGTTTTTAATTT	84132
rs571164777	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6152359	TATATACTGGGTGCC[C/T]TCCTGGAAACGTCAG	84132
rs571165084	snp	G/T	0.00676609	0.0577691	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080609	AGGAGCCTGAGGCAG[G/T]ACAATCGCTTGAACC	84132
rs571195125	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152661	CTCTGGCCTCACCTA[A/G]GCCAGGTAGCGTGAG	84132
rs571211999	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6157635	GAACTCTTGGTTTTA[A/G]AGCATTTTTGATAGA	84132
rs571315875	snp	A/C	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6121169	TTTCTAGTAAAGAGA[A/C]CTCCATTACATTGTT	84132
rs571326614	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6113023	ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG	84132
rs571326930	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136837	TCAAGTGAGACTGTG[C/T]CTCACTGTTTTGCCC	84132
rs571332932	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125785	TTTGATGCTCAGGGG[G/T]TGTTTATTTTACTTT	84132
rs571342228	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106139	AATTAGGGTCAGTTT[C/T]ACTTTCTCTTCTGTA	84132
rs571365775	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6111570	GGTAGATTGTTTTTA[C/G]TTGCTAGAATATTAT	84132
rs571420952	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105717	GTGTGCCTCTCTAGC[G/T]TTTTTTATTTTCGGG	84132
rs571434225	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143473	CTGAAAAACTCTAAT[G/T]TTGATCATTCATTAA	84132
rs571434505	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136874	GTCTTGAACTCCTGG[C/T]TCAAGTGATCCTCTT	84132
rs571459782	in-del	-/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113629	TTGTTTTTGTTTTTG[-/T]TTTTTTTTTTGAGAC	84132
rs571557555	snp	A/C	5.16729e-05	0.00508269	intron-variant	USP42	GRCh38.p7	7:6147928	GAACATTTTTATGTT[A/C]ATTTTTAAAATGTAA	84132
rs571599064	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136214	TCTCCATGTTGGTCA[A/G]GCTGGTCTCAAACTC	84132
rs571609530	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6118399	TGGCGGTGTGCGCCT[A/G]TAGTCCCAGCTACTT	84132
rs571612363	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6135629	TGCACTCCAGCCTGG[A/G]TGACAGAGTGAGACT	84132
rs571657479	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104216	GCTTCCCGAGTAGCT[A/G]GGACTACAGGCGCGC	84132
rs571689135	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114791	TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGTCT	84132
rs571693525	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6146839	TGCGGGCAGTAATGG[A/C]GTGGGCCAGGAGCCA	84132
rs571712011	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6136497	TATTCAATTTAATAT[A/T]ACAAATTTTAAACTA	84132
rs571735402	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123612	AGCCTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	84132
rs571764440	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6091787	GATGGGGGTGCAAAG[G/T]GGGGTGGTGTCTAGC	84132
rs571769682	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6078960	CCCTTTTGGTTTTAA[A/G]GCCTCCACCCCAGTG	84132
rs571798592	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123438	GGAGGCCAAGGCGAG[C/G]AGATCACGAGCTCAG	84132
rs571804221	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6101251	CAGTAAGGAGGACCT[C/G]GGTGGGGCATTAACA	84132
rs571818150	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096417	GAGGAGGGATCCCAA[C/T]GGTGCAGATGCAGTG	84132
rs571839600	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6131313	AAACCCTGTCTCTAC[C/T]GAAATACAAACATTA	84132
rs571854293	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6119954	CGGTTCTCTTGCCTC[A/C]GCCTTTTTTTGTTTT	84132
rs571863187	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145968	CCAGCAGCTCCGGAG[G/T]CTGAGGCAGGAGAAT	84132
rs571883351	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097552	GTTGTGATTACAAGC[A/T]TAAGCCACTGCGCCC	84132
rs571917598	in-del	-/G	0.00795532	0.062565	intron-variant	USP42	GRCh38.p7	7:6119711	TGTTGTTGTTGTTTT[-/G]TTTTTTTTTAGTGAC	84132
rs571998029	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104662	AAGGAGCCCTTTCGC[C/T]GGCGCGCAGACGCGC	84132
rs571998104	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6097097	GTTTAGTAGAGACGG[A/G]CTGCTATCATCCTCT	84132
rs572022908	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119340	TTCTCTGGGTGTGGC[A/G]GCAAGCGCTAGTCCT	84132
rs572025378	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6123611	GAGCCTGCAGTGAGC[C/T]GAGATCGCGCCACTG	84132
rs572065477	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103353	ACCAGCCTGACCAAC[A/G]TGGTGAAACTCTGTC	84132
rs572076657	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6122771	CACTGTGTCCAGCCT[A/G]ATTTTTTTTTTAAAT	84132
rs572088576	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6082145	ATCCTTTTTTTTTTT[C/T]TGAGATAGAGTCTCG	84132
rs572094445	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6158534	TGATTGAGGGGTAAA[C/T]GGTCCTTAGAGTGTG	84132
rs572102752	in-del	-/T	0.00279162	0.0372561	intron-variant	USP42	GRCh38.p7	7:6100542	CCATGTTGGCCAGGC[-/T]TTGTCTCGAACTCCT	84132
rs572111405	snp	C/T	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6133929	AGCGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	84132
rs572114712	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6101708	TGGGGCAAGGTAGAG[A/G]GGGAGGTGTAACCCC	84132
rs572130904	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158122	GGTTGGAAATAATCC[C/G]AAAGAACAATGCGTT	84132
rs572131553	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094897	GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCT	84132
rs572138682	in-del	-/T	0.403509	0.197319	intron-variant	USP42	GRCh38.p7	7:6085286	ACCATGCCCGACTAA[-/T]TTTTTTTTTTTTTAG	84132
rs572180622	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6108683	ACAGGGTTTCACCAT[G/T]TTGGTCAGGATGGTC	84132
rs572200118	in-del	-/GGAAA			intron-variant	USP42	GRCh38.p7	7:6160133	ATTTTTCCCTTGAAA[-/GGAAA]CTTTGTCCAAATGTG	84132
rs572221349	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6150868	TAGGCCAGGGCTCTC[A/G]GTCCTGTGAAGAAGC	84132
rs572254862	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113836	CTGTGTTAGCCTGAA[C/T]AGTCTCGATCTCCTG	84132
rs572277214	snp	A/C	3.38026e-05	0.00411098	missense	USP42	GRCh38.p7	7:6150259	GCCAGCCTGCCCTGC[A/C]CTCAGAAAATCCCTT	84132
rs572291599	in-del	-/A	0.36021	0.224397	intron-variant	USP42	GRCh38.p7	7:6123833	AGGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	84132
rs572308588	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100948	GCTGGGACTATAGGT[G/T]TGTGCCACTGAGCCT	84132
rs572334979	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096465	ATAGGTTGCATGTGA[C/T]GGGAATGAAGCTATA	84132
rs572359845	snp	C/T	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6149623	GACCATTGAAAGACA[C/T]GCCAAGCAGTTCCAT	84132
rs572398934	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112466	AAAAGAAAAAAGAAA[A/G]AAAAAAGAGAGCATG	84132
rs572412826	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077293	GGGAAATGATACCCT[C/T]GTCAAGTTCCCTCTT	84132
rs572423768	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144587	TTAAAATTAAATAAT[C/T]GGCCGAGTGTGGTGG	84132
rs572493113	snp	C/G	0.000399281	0.0141238	missense	USP42	GRCh38.p7	7:6153958	GCCCCCGAGGAGCCT[C/G]CGCCCAGCGCCGGCG	84132
rs572513801	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133636	CCTCCCATCCCACAT[C/T]AGCCTCTGGAGTAGC	84132
rs572542304	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6110901	TCAAATACTTCACTG[A/C]AGATTTTAAAATAAA	84132
rs572582862	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143616	TCTTCAAGACCAGAG[A/G]GATTTTGCCTTTGTT	84132
rs572625520	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6142109	GTGAGCATCCTCTAT[A/T]TTTTTGTTCACTTTA	84132
rs572652562	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080793	CTTCCTATGTCAGTA[C/T]AGCATGGTAGTCCAT	84132
rs572685265	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6157706	AACCTGTAGCATTCT[A/G]AGTGCACCCTGATGC	84132
rs572701246	snp	G/T			intron-variant, utr-variant-3-prime	USP42	GRCh38.p7	7:6152985	GAAGAACTAGAGGAA[G/T]TGCGGCCAGGCGCGG	84132
rs572711370	in-del	-/ACTT	0.000789134	0.019848	frameshift-variant	USP42	GRCh38.p7	7:6157002	GTGAGAAAACGAAAC[-/ACTT]ACGGATGGAAAGCAG	84132
rs572716694	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137744	GAGTGCAGTGGTGCA[A/G]TCTTGGCTCACTGCA	84132
rs572721443	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161706	CATCCCACCTCGGAC[A/G]GGCAAAGGAAAATTG	84132
rs572756108	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6139002	TGGGAGTTTTCCAAC[C/T]AACATATTATTATAA	84132
rs572758903	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	USP42	GRCh38.p7	7:6160953	ATATTTAATTTAAAG[A/G]CTTATTTAAAAACTC	84132
rs572763983	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132081	GGGACTACAGGCGTT[C/T]ACCACCATGCCTGGC	84132
rs572786407	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092471	GGCATGCGCCACCAC[A/G]CCCGGCCTCAAGGAC	84132
rs572790457	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6135608	AGTGAGCCAGGGTCA[C/T]ACCACTGCACTCCAG	84132
rs572798429	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6098388	CGTAGTATCCATTCC[C/T]GGGCTTATTTTCAGT	84132
rs572819702	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144978	AAAGAAAATAATAAA[C/T]GCAGCAGGATGGCCT	84132
rs572819794	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6138591	TGGTGTAAAGCAGGG[G/T]TCCCTAACCCCTGGG	84132
rs572864926	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099285	AGTGGCGCGATCTCA[C/G]CTCATTGCAACCTAG	84132
rs572866913	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159070	AGGCCGCTGCCCGGC[C/T]CCGCCTCACCCAGCG	84132
rs572878951	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6106275	GTGTGTTTTCTCTTA[C/T]AACGGAAATGCTATG	84132
rs572936758	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125939	GAAATCCCATGTACC[C/G]TTACTGAACCTCCCC	84132
rs572940041	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6105811	CGGAACAAGTTTTCC[C/T]ATCTAGGACTTTAAC	84132
rs572978509	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6153542	GCTGCTAAATGACGA[A/G]TTAATGGGTGCAGCA	84132
rs572987610	snp	A/G	0.00517822	0.0506191	intron-variant	USP42	GRCh38.p7	7:6118892	GTTTGTCTTGACACC[A/G]TAACACAATGTTTTG	84132
rs572991271	snp	A/C	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6120367	CCTGCCTCAGCCTCC[A/C]AGGTAACTGGGATTA	84132
rs572998831	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6125422	TTGAACCTTGGAAGC[A/G]GGGGTTGCAGTGAGC	84132
rs573011354	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6130802	GGAAGACAAAGATTT[C/T]ATGCTCACAGGGCAC	84132
rs573056532	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148065	GAAAACGGCCGAGCG[C/T]AGTGGCTCAAGCTTG	84132
rs573108921	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6127511	CTGGATGTCATTTGC[C/T]CCAGCGTCATTTTCT	84132
rs573119157	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147647	TTTCATCAGGTTTCC[A/G]CCTGAGGGGTTAAAT	84132
rs573157385	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6089686	TACAGGCATGCACCA[A/C]CACGCCTGGCTAATT	84132
rs573161795	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121855	TTGTAGAGACGAGGT[C/G]TCACTATGTTGCCCA	84132
rs573171618	snp	C/T			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161682	CGAAGTCGGCACCTT[C/T]GGCCAGGCCATCCCA	84132
rs573172819	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6156512	TGGAGTGCGGTGTTG[C/T]AGTCGTAGCTCACTG	84132
rs573173076	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126870	AGCATGTCTTCATTT[C/T]TCTGGGATAAATGCC	84132
rs573188154	in-del	-/AGTT			utr-variant-3-prime	USP42	GRCh38.p7	7:6161129	ATCAATCAATTTCCC[-/AGTT]AGTTATGATGAGTAT	84132
rs573243927	in-del	-/GGC	0.0588605	0.161139	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104914	CGGCGCTGACCCGGA[-/GGC]GGCGGCGGCGGCGGT	84132
rs573250070	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6123522	CAAATATTAGCCAGG[C/T]GAGGTGGCGGGCGCC	84132
rs573252062	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131525	ATACAGAAAAAAATA[A/C]ACACAGAAGCTGAAG	84132
rs573266167	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6136348	GGTGAAAAAAACCGA[A/G]CCCGTCATGTATTAG	84132
rs573287785	snp	C/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6085361	GGATCTCCTGACCTT[C/G]TGATCCACCAGCTTT	84132
rs573332510	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159739	CATCCTTCACGCAGG[C/T]AGAGTCGCCCTGTTC	84132
rs573349229	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6143641	TTTGTTTTAAATTCC[A/G]CAGACATTTCTAATA	84132
rs573363672	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152792	TAATTTACTACAGAA[C/T]GTTTTGCTAAAGCCT	84132
rs573404462	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6116517	GGCTCAGATTCATGT[G/T]TGTATGTTCTGGGGC	84132
rs573441749	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	USP42	GRCh38.p7	7:6084462	CCGGACACTAAAGGA[C/T]ATCACTCTGAGCCTG	84132
rs573504575	in-del	-/C	0.00914312	0.0669923	intron-variant	USP42	GRCh38.p7	7:6105938	TCAATACCCTGACAG[-/C]CAAAACTGTTTGAGA	84132
rs573505526	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121301	GATGCCTTTTACCAG[C/G]TTGAGTTGTTTGATG	84132
rs573525366	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151957	GTTGACCGTATGTAT[G/T]AGGTACATGACTGTA	84132
rs573525927	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110558	TCCATATAAATGAGC[C/G]TCTTCAGAAAAATGG	84132
rs573541612	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114911	TAGCCAGGATGGTCT[C/G]GATCTCCTGACCTCA	84132
rs573544493	snp	C/T	0.00676609	0.0577691	intron-variant	USP42	GRCh38.p7	7:6117169	CCCTCAAAAGTTCCC[C/T]GATGCCCCTTTGAAA	84132
rs573565289	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6109762	CTGGATATCAGTGGC[A/G]CGGTTTTGGCTCTCT	84132
rs573609061	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6127996	GTGTGATCATAGCTC[A/C]CTGCATCCTCAAAAT	84132
rs573619404	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079669	GAATGTGCTTTATGT[C/T]TATGCTCTTATTCTC	84132
rs573677237	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119927	GGCTGGTCTTGAACT[C/T]CTACGCTTAAGCGGT	84132
rs573698925	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151507	CAGTGGTGCGATCTC[A/G]GCTCACTGCAGCCTC	84132
rs573772350	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097243	CCGTGGTCCTGGTAA[A/C]ACGGTGTTTTCCAGG	84132
rs573804440	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124645	CCTTTTATTTTGAGG[C/G]ATTATACCTTTTACA	84132
rs573840712	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6145458	AGTACCCTCTACCTG[A/T]ATATGTGGAATGATC	84132
rs573848924	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083889	GGTCTCTAGCAAGGA[C/T]AGATTTGTACTGATC	84132
rs573908181	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6136809	TTTTTCGGTTCTTCT[-/T]TTTTTTTTTTTTTCA	84132
rs573922210	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134065	CCAGCTAATTTTTTT[G/T]TATCTTTAGTAGAGA	84132
rs573966290	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6132584	GGCTGGTCTCAAACT[C/G]CTGACCTCAAGTGAT	84132
rs574035192	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6139955	CAGACCTCCCTGTGT[C/T]CTGGCCAGGAAGGGA	84132
rs574076467	snp	A/G			missense	USP42	GRCh38.p7	7:6154972	GACAGAACTGCACTT[A/G]TAGCCGGAGACAACT	84132
rs574079482	snp	C/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113863	CCTGACCTTGTGATC[C/T]GCCCGCCTCGGCCTC	84132
rs574087722	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6108606	CTACCTCAGCTTCCC[A/G]AGTAGCTGGGATTAC	84132
rs574127316	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6128321	GGTCTGGAGTGCAGT[A/G]GTGCGATCATGGCTC	84132
rs574148503	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108267	ATTTGGCCAGGTTCT[A/G]TGGCTCATGCCTGTA	84132
rs574194747	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133609	AGCCTCCAACTGCTG[A/G]GCTCAGGTGGTCCTC	84132
rs574200995	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6133116	TTCTGTCAAATTTGG[A/T]CAACTTTCAGTGACT	84132
rs574304607	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6095829	CTGCAGTGGTGTGGT[C/T]ACATCTCACTGCAGT	84132
rs574321497	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6130134	AGAATTGTAGGCATG[A/C]GCCCCCGCGCCTGGC	84132
rs574332564	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6158089	TTGGAGTTAAGAATG[C/G]TTTTAACCTTTTTAA	84132
rs574353054	snp	G/T	0.00795532	0.062565	intron-variant	USP42	GRCh38.p7	7:6130537	GTCACAACGTGGGGT[G/T]GGACAGGGTTTGTTC	84132
rs574383185	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094274	GACCTCCTGGGCTCA[A/C]GCGATCCTCCCACCT	84132
rs574385852	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6129587	AAAAAAGGACGAGGC[A/G]CGGTGGCTCATGCCT	84132
rs574409747	in-del	-/TAAGA	0.00398564	0.0444627	upstream-variant-2KB	USP42	GRCh38.p7	7:6077007	AGCCTCCTGAGTAGC[-/TAAGA]TTACAGGCACATGCC	84132
rs574451925	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151167	CCATGAATGGAGCTG[A/G]CAGGACTGGAGGGTG	84132
rs574474402	snp	A/C	0	0	intron-variant	USP42	GRCh38.p7	7:6111849	CGATCTTCTGACCTC[A/C]TGATCCACCCACCTC	84132
rs574477752	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093695	CTCTCCCTCTTTCTC[C/T]CCCCCTCCCTTCTTT	84132
rs574477867	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6112800	GTGTGGCCCAAGACA[A/G]TTTGTCTTCCAGTGT	84132
rs574481162	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6088546	ACAGGCATGAGCCAC[C/T]GTGCATGGCCTCCTA	84132
rs574534638	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077201	AATCTTGTTTGTGTA[C/G]TGTCTCTAATTCCTT	84132
rs574542535	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161815	TTATTTAGTGAACAC[A/G]GTATCTGCAAGAGCT	84132
rs574556226	snp	G/T	0.00398564	0.0444627	upstream-variant-2KB	USP42	GRCh38.p7	7:6077710	TACTAAAAATGCAAT[G/T]TTTTTTGCTCTTACT	84132
rs574602791	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6118825	AAAAAAAATCAGTAA[A/G]CCATATCAATACGAT	84132
rs574615486	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148269	TTGAGCCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	84132
rs574618963	snp	A/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077787	CACCTTCCGGTTTCA[A/T]GCGATTCTCCTGCCT	84132
rs574632327	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6118337	GACCAGTTTGGGCAA[C/T]ATGGTGAAACCCTGT	84132
rs574632616	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6123589	ATGGCATAAACCCCG[C/G]GAGGCAGAGCCTGCA	84132
rs574697329	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6106873	GCCCCACCTGTAGGT[G/T]GTTGTTTTAATGCTC	84132
rs574710481	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6102933	TGAGATGGAATTGTT[A/G]AGCGAAGAAAGGCTG	84132
rs574731796	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6112994	CTGCAATCTCTGCCT[C/G]CTGGGTTCAAGCAAT	84132
rs574783613	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6117443	TGTTTCTCCATTTGT[C/T]TATTGATGGGCATCT	84132
rs574820248	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6081966	ACATAAAATAACATA[C/T]TCTGTGAGACAATAA	84132
rs574852764	snp	A/G/T	0.000148376	0.00861213	missense	USP42	GRCh38.p7	7:6153907	GATCCCGGCACCCCC[A/G/T]CTACCAAAGAAGGCG	84132
rs574876202	snp	G/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6157374	AGAACTCTTGGTTTG[G/T]TTTGGTTTTATTTTA	84132
rs574886376	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6127844	TGTGTCTTAATTTGG[C/G]GGGATTAACATCTTT	84132
rs574889954	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153475	GTTTCCAGAGATAGT[A/G]GTACTAGCCTAATAT	84132
rs574911841	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080179	AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG	84132
rs574927092	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100206	CAAAAACCAGAGAGA[C/T]TGAATAAGCCAACAC	84132
rs574979910	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148005	ACATCTGAATTTCTT[C/G]TCACAGTTTAATCAA	84132
rs575007598	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126829	TGGAGCTGCTATAAA[C/T]GTGAGTGTATATAGC	84132
rs575014674	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6144537	TCAAAAACTAAATAG[C/T]ATGCAAGAGAAATAA	84132
rs575028374	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153072	GGTCAGGAGTTCGAG[A/G]CCAGCTTGGCCAAGG	84132
rs575042219	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6147546	TACCCAGTTATCCTT[C/G]TTGTCTCCTGATCTG	84132
rs575096251	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6136913	TGAGTAGCTGGGATT[A/G]CAGATGTGCACCACT	84132
rs575103403	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143178	GAGCCCGGAGTGTCT[C/T]GATGTGTGTGTTTCT	84132
rs575105104	snp	A/C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092428	AGGGGATCTGCCCAC[A/C/T]TTGGGCTCTCAAAGT	84132
rs575113660	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105766	CCTGGAACGGGGGAT[C/G]CGTTGCAGATGTTGG	84132
rs575160985	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6097791	GAGGCGGGGTTTTAC[C/T]ATGTTAGCAAGGATG	84132
rs575240808	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6104973	CGCCGGGCGGCTGGG[C/T]TGTGTGCGGCGGCGG	84132
rs575280880	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131344	GCCGGGTATGGTGGT[A/G]CATGCCTGTAATCCC	84132
rs575282989	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6142637	CCTGTAATCCTAACA[A/G]TTTGGGAGGTCGAGG	84132
rs575290136	snp	A/C	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6148757	ACACGGTCTAGCTGC[A/C]TGCTTTATTTTATGG	84132
rs575326198	snp	A/T	0.00199481	0.0315187	utr-variant-3-prime	USP42	GRCh38.p7	7:6160875	GTTCCTCCAAGTTAG[A/T]CATCTGGTGCAAGAC	84132
rs575330356	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	USP42	GRCh38.p7	7:6130285	TCCCCACTCAGCCTC[C/T]GTTGGCACCCCAGGT	84132
rs575332216	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135757	TTATTTCATTTCAGG[C/T]GTGTGCCCCTGATTT	84132
rs575344722	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6135206	AGCTAGGAGCACTGG[C/G]TTTCAAATTTGAAAG	84132
rs575355820	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121941	GCTAGGATTATACCA[C/G]CATACCCAGCTTTCT	84132
rs575365753	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110341	TCTGATCTCTCATAC[A/G]TTCTTTATAAAAATT	84132
rs575377138	snp	A/C	0.000133806	0.00817833	synonymous-codon	USP42	GRCh38.p7	7:6156916	CTTGGAGACTGTCGC[A/C]CAGTTCCGGAGAGCC	84132
rs575398743	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152393	CAGTGAAAACCGTGC[C/T]AGTGACACACCCGTA	84132
rs575412043	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6160510	TAAGCCCTACACGCC[A/G]CCGCCTGCCTCCAAC	84132
rs575436915	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6152094	GGTCAGGAGTGAGAG[A/G]AAGGGAATTTGTCAT	84132
rs575460757	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136984	GAGCTTAGCAAATTG[A/G]TGGATAAATTTTACT	84132
rs575529628	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080318	ATGTTATTAATACTG[C/G]AGGTCTTTTTATAGT	84132
rs575531636	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6125566	TCCATCTTTCCTTTC[A/C]CATCTTTGTGCTATT	84132
rs575542672	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6126476	TATTTTTAGTAGAGA[C/T]GGGTTTCACCGTGTT	84132
rs575549252	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6084710	CTCCTCACCTGATAT[C/T]GCAAGGACTCTTTTT	84132
rs575570328	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6084357	ATCTATTGTAGGTTT[C/T]CAGTAACTTTTAGTC	84132
rs575574982	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6159659	CCAGACCCAGGCCAC[A/G]CGCTTGGGGACAGAC	84132
rs575622331	snp	C/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6131616	TGGAGAGAGTGGGAG[C/T]GGGATTTTGCTGGGC	84132
rs575639350	in-del	-/AT	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6155640	CAGACAACAGGAGGC[-/AT]ACACTTTTCCTGTGC	84132
rs575662644	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6119896	TTTTGTAGAGACAGT[C/G]TCACCATGTTGCCCA	84132
rs575704172	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6091309	AGCTCACTGCAGCCT[C/G]AAACTCCTGGTCTCA	84132
rs575706830	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6079486	TAAATAAATAAATAA[A/G]TAGTACTTAGTATTA	84132
rs575707178	snp	A/G			utr-variant-5-prime	USP42	GRCh38.p7	7:6093053	TGACTGAGTCTCCGT[A/G]TGGGCTGCTGGGACA	84132
rs575716608	snp	C/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6097226	GATGCTGTCTCTGCC[C/G]TCCGTGGTCCTGGTA	84132
rs575716660	snp	A/C	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6090437	ATTTATATATATGCC[A/C]GGCACAGTGGCTCAC	84132
rs575739589	snp	C/G			downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161368	TAATTCACTGGTCCT[C/G]CATCAGGAGATGGAG	84132
rs575761982	snp	G/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114375	ATATAAAAGAGTAAT[G/T]ATAATGAACTCTCAT	84132
rs575767754	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089646	CAAACAATTCTCCTT[A/C]CTCAGCCTCCTGAGT	84132
rs575777890	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121260	CAGTCTTTTACCATT[A/G]AGTATGGTGTTGTAG	84132
rs575778744	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6096616	AGGTTTGGGGAAGAA[C/T]AGGTGCAGAGCAGGA	84132
rs575926900	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6102328	CATATTGGCCAGGCT[A/G]GTCTCGAACTCCTGA	84132
rs575928780	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6085908	GTGAGCCACCGTGCC[C/G]AGCCTATTAGTCTAT	84132
rs575930281	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6085229	GGTTCAAGTGATTCT[C/T]CTGCCTTAGCCTCCA	84132
rs575938098	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6089835	CGCGCCCAGCCTCTT[C/T]ACCTGACTTTCTGAT	84132
rs575949509	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113873	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	84132
rs575950460	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	USP42	GRCh38.p7	7:6077960	CCAAAGTGGGCGTGA[A/G]CCACCGGGCCTGGCC	84132
rs575962072	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6107894	TTCTTAGTTCATTGA[A/C]ATTGACAAACATCTT	84132
rs575968406	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6077344	TGTGTGATGATTCAT[G/T]TACGGAGAATTGATG	84132
rs575981426	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6082376	CTCGTGATCCGCCTG[C/T]CTTGGCCTCCCGAAG	84132
rs576008744	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6083779	AACTCTCCATCTTAG[A/G]GCATGTAAATTCCTC	84132
rs576015178	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6106986	GTGAGGAACATGCAA[A/G]TATATGAATCTTAAG	84132
rs576061319	snp	G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6123718	CTAGGCGTGGTGGTG[G/T]TCTTCTATAGTCTTA	84132
rs576071801	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103586	TGGACAGTGGCGCAC[A/C]GGTGGGGTCAGGCGG	84132
rs576088137	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6082958	ATATATATATTTATT[A/T]ATTTTAATTTTATTT	84132
rs576090865	snp	C/T	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6129518	GCCAAGATTGTGCTA[C/T]TGCACTCCAGGCTGG	84132
rs576159376	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6141425	GCCAGGATGGTCTTG[A/T]ACTCTTGACCTCGTG	84132
rs576201917	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103004	GTAAACATGAGTTGG[C/T]GTAAAGGGTTAGATC	84132
rs576214515	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6108795	CAATATTAAAAAAAA[A/T]ATTTTTTAAGGCCAT	84132
rs576227800	snp	C/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6089201	AGGCGCCCGACACCA[C/T]GCCTGGCTAATTTTT	84132
rs576241685	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6095034	CTCAAGGGATCTGCC[C/T]GTCTGGGCCTCCCAA	84132
rs576244552	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6141041	AGTCATTTTATGTAA[C/G]TGTAGTTCATTTATA	84132
rs576245436	snp	C/G	3.01001e-05	0.00387932	missense	USP42	GRCh38.p7	7:6154642	CGGAGCGGGGTGGAG[C/G]TGGACTGGGTCAGAC	84132
rs576273516	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146500	GAGACCACATGTCTA[C/T]AAAATACGAAAAAAT	84132
rs576303960	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	USP42	GRCh38.p7	7:6078462	AAAAAATTAGCCGGG[C/T]ATGGTGGCGGGTGCC	84132
rs576305846	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6146033	CGCCACTGCACTCCA[C/G]CCTGGGTGACAGAGT	84132
rs576336838	snp	A/G	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6145376	AGGTTTTTTAAATGC[A/G]TTAGGTTTTTGCTAG	84132
rs576341926	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6100998	AAACCAGGATATCTA[C/G]AAGTGAGGCTTGAGA	84132
rs576445890	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6145012	ATACACTTAGATTCC[A/G]CTATCCTCCCGGTTA	84132
rs576453100	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151355	TTTACTTTATAGACT[G/T]TTAATTTTAAACTGT	84132
rs576478165	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6139032	AGATATATTTTGGGG[A/G]GTACAACTTAGGCTT	84132
rs576506193	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6132729	CAGGCTGGAGTGCAG[C/T]GTCGAGATCTCGGCT	84132
rs576516400	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6128180	CTGGTCTCGAACTCC[C/T]AGCCTCAAGTGATCC	84132
rs576549605	snp	G/T	0.00874735	0.0655527	intron-variant	USP42	GRCh38.p7	7:6089690	GGCATGCACCACCAC[G/T]CCTGGCTAATTTTTT	84132
rs576559500	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112984	TCTCGGCTCACTGCA[A/G]TCTCTGCCTGCTGGG	84132
rs576564526	in-del	-/A	0.00597247	0.0543191	intron-variant	USP42	GRCh38.p7	7:6146662	GAGCAAGACTGTCTC[-/A]AAAAAAAAACCAAAA	84132
rs576569569	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6137783	CTCTCGGATTCCAGC[C/G]ATTTCTCCTGCGTCA	84132
rs576603768	in-del	-/AG			intron-variant	USP42	GRCh38.p7	7:6087173	AGTAGCTGGGATAAC[-/AG]GGGTGTGCCATCACG	84132
rs576627460	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6112509	TACATTTGTTATAAT[A/G]ATACAAATGTGGTTA	84132
rs576628727	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6158013	CAGTGGACCTAGAGC[A/G]GAGGCTGGCAAACTG	84132
rs576631277	in-del	-/CCTTCCCTTCCC	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6086658	GCCTTTTCCTTTCCT[-/CCTTCCCTTCCC]CCTTCCCTTCCCCCT	84132
rs576737469	snp	C/T	0.00199481	0.0315187	intron-variant	USP42	GRCh38.p7	7:6113050	CTGGGACTACAGGTG[C/T]GCGCCACCATGCCCA	84132
rs576774860	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6112464	CAAAAAGAAAAAAGA[A/G]AAAAAAAAGAGAGCA	84132
rs576785161	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	USP42	GRCh38.p7	7:6161024	GTAATGTCTGATACT[A/G]GAAACTAATTTGCTT	84132
rs576787993	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6134031	GAGTAGCTGGGACTA[C/T]AGGTGCCCACCACCA	84132
rs576818347	snp	A/G	0.00159617	0.0282053	intron-variant	USP42	GRCh38.p7	7:6133662	GTAGCTGAGACTACA[A/G]GCACGTGCCACCACA	84132
rs576853371	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121861	AGACGAGGTCTCACT[A/G]TGTTGCCCAGGGTAG	84132
rs576891971	snp	C/G/T	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6141603	TTGCTCCATTGCCCA[C/G/T]GCTGGAGTGCAGTGG	84132
rs576903857	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6139828	TCCCACACAGGCCGC[A/G]GTGCCCGGAGGCTGC	84132
rs576913643	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6094272	TTGACCTCCTGGGCT[C/T]AAGCGATCCTCCCAC	84132
rs576914083	in-del	-/CAAT	0.00281237	0.0373935	utr-variant-3-prime	USP42	GRCh38.p7	7:6161113	TTTGTGGAACTGTTC[-/CAAT]CAATCAATTTCCCAG	84132
rs576916485	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6137617	CCCGTCTTGGCCTCC[C/T]AAAGTGCAGAGATTA	84132
rs576919408	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121390	TATTCTATGTATTAC[G/T]GGCTTTGATTTGCTA	84132
rs576926520	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6093160	CTCTCTCCCTCCCTC[C/T]CTTCCCTTCCTTCCC	84132
rs576926662	snp	A/C	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6099956	TGACAGAACGAGACT[A/C]CCTCTCAAAAAAAAA	84132
rs576928979	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081749	GCGCCTACGTGGACT[A/G]CGGGTTCGCTCCGGG	84132
rs576931069	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6149229	TCCTCCTTCCTGGCA[C/G]TCTGCATCAGCGAGC	84132
rs576951616	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6092287	GGTTCAAGTGATTCA[C/G]CTGCCTCAGACCTCC	84132
rs576959505	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6099436	AGCCAGGATTGTCTC[A/G]ATCTCCTGACCTCAT	84132
rs576984100	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081376	CCGCGGGGAGGTAGA[C/T]GGCGGGCGGCGCAGC	84132
rs576984902	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6099359	AGCTGGGACTACAGG[C/T]ACCCGCCACCATGCC	84132
rs577021085	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6147524	ACACAGTTTAAAGAA[C/T]GTCATTTACCCAGTT	84132
rs577036158	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143254	TATTGGGCAGATTCG[A/G]TGGGAGGAGAGAGGT	84132
rs577094624	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6144393	TGTATAATCTGAAAT[C/G]CAAAGAGGACTTCCT	84132
rs577204859	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104385	CGCGCCCGGCCCAGA[C/T]CTTGTTTCTAAGAAA	84132
rs577228740	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160403	CACCGCCAGTTCCCT[C/G]ATTTCCACTCAGGAA	84132
rs577255465	snp	A/C	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6126399	ACGCCATTCTCCTGC[A/C]TCAGCCTCCCGAGTA	84132
rs577297995	snp	A/T	0.000798403	0.0199641	intron-variant, missense	USP42	GRCh38.p7	7:6152965	TCTTTAGTCTTAGTT[A/T]TTAGGAAGAACTAGA	84132
rs577301339	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6086099	GGTTTGCAATGCCAA[A/G]ATCTTGGCTCATTGC	84132
rs577317070	snp	G/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6143811	AATTGAGAGGAAGTT[G/T]TGTTAACCTAATTTT	84132
rs577330871	snp	A/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079828	TTGGTGAAATTTGTC[A/T]TTCTTACTCAAGTTT	84132
rs577331767	snp	C/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6121015	TGGAACCTTAAGTCA[C/G]TTATTAATTCTAGTA	84132
rs577404333	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6111763	GCCTGCCACCAAGCC[C/T]GGCTAATTTTTTTTT	84132
rs577411648	snp	A/G	0.00358779	0.0422022	intron-variant	USP42	GRCh38.p7	7:6132650	AGGCATGAGCCACCA[A/G]GCCAGCCTATGTAAT	84132
rs577414093	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6105922	ATGTTGGTTATGTAA[A/G]GTCAATACCCTGACA	84132
rs577425564	snp	C/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6097750	CGGCCGCCACCATGC[C/G]CCGCTAATTTTTTGC	84132
rs577461153	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6148055	CAAATATACAGAAAA[C/T]GGCCGAGCGCAGTGG	84132
rs577488451	snp	A/G	0.00953873	0.0683987	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104756	CGTCTGCCTTCGCCC[A/G]CGGCTCTTGGGCGAC	84132
rs577496769	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6150650	TTATAATGTATAGGA[C/T]TTATTAACTTGCCTT	84132
rs577552294	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6110298	GTTGCTGACTGGTTG[C/T]TTCATTTTATAGGCC	84132
rs577580385	snp	A/G	0.00119737	0.0244387	intron-variant	USP42	GRCh38.p7	7:6147002	GTTGTGGCTGCATAC[A/G]CTTTTCACTCACTCA	84132
rs577679280	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114421	CTTTGACATTTATCA[A/G]CTTACGGGCAGTGAT	84132
rs577696717	snp	C/T	0.00914312	0.0669923	intron-variant	USP42	GRCh38.p7	7:6141365	ATGTGCCACCATGCC[C/T]AGCTAATTTTTGTAT	84132
rs577724569	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6133232	AAACCATGCCTCTTC[C/G]CAAAAACCTCCTTTG	84132
rs577729879	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6131548	AGCTGAAGTAGAGCA[A/G]TGATTTCTAAAGGTT	84132
rs577765145	snp	A/T	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6091974	AGTCCTCAAGGACGT[A/T]TTTTTTCTTCTTCTT	84132
rs577768442	snp	A/C	0.00318978	0.0398085	upstream-variant-2KB	USP42	GRCh38.p7	7:6078588	GCCTGGGAGACAGAG[A/C]AAGACTCCATCTCAA	84132
rs577769040	in-del	-/G/TTG	0.0126979	0.078662	intron-variant	USP42	GRCh38.p7	7:6119691	TTTAGGCCTTGTTTT[-/G/TTG]TTGTTGTTGTTGTTG	84132
rs577801434	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6155816	GAGTGCAGTGATGCC[A/G]TCATAACTCACTGCA	84132
rs577825081	snp	A/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6120705	TCTTCTGCTTCAGCC[A/T]CATGGGTAGCTGAGA	84132
rs577888454	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6160080	AGAGTCACTGGTTTT[A/G]TACCTGACCCTTGTG	84132
rs577952084	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6092826	GAAGATTAAATATAT[A/C]CCTCCTTGAACACTT	84132
rs577981262	snp	A/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6136387	TACATTTTGTCGTAC[A/G]TGGCTATGTCTTTGA	84132
rs578027374	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6136023	TTTTTTTTTTTTTTC[A/G]AGACAGAGTCTTGCT	84132
rs578061308	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113984	AAAATTAGTCTTGCC[A/G]TTGATGATTTTCAGC	84132
rs578069707	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103536	AAAAAAAAGAAAAAG[A/G]AAATCCCTTTCTGTA	84132
rs578071085	snp	C/G	0.000798403	0.0199641	intron-variant	USP42	GRCh38.p7	7:6095890	GCCTCAGCCTCCTGA[C/G]TAACTGGGACCACAG	84132
rs578077520	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6085147	TATTTTGAGACAGAT[C/T]CTCACTCTGTCATCC	84132
rs578090125	in-del	-/TT	0.0973687	0.197999	intron-variant	USP42	GRCh38.p7	7:6126288	ATACGCCACAGTTTC[-/TT]TTTTTTTTTTTTTTG	84132
rs578102124	snp	A/G	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6151626	TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTTAC	84132
rs578143093	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6095814	TCACTGTTACCCGGG[A/C]TGCAGTGGTGTGGTC	84132
rs578216682	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6090292	GCAACAATATTGAAA[C/T]TCTGTCTCAAAAAAA	84132
rs578247023	snp	C/T	0.000399281	0.0141238	intron-variant	USP42	GRCh38.p7	7:6124766	AAATCTTTTTCCTGC[C/T]TTCTTTTGGATTGAT	84132
rs745311841	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6152507	AATGGCCCCCGGCGG[C/G]TGGGAGTGCCCTCAC	84132
rs745323165	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131815	ATTTTATACACAATG[A/G]TCAGGATTTGTTGTA	84132
rs745386267	snp	A/G	1.73788e-05	0.00294772	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116859	TGAAAGTAGGGTGTG[A/G]ATGAAAACCCAGCAC	84132
rs745417556	snp	C/T	3.07602e-05	0.00392163	synonymous-codon	USP42	GRCh38.p7	7:6153921	CGCTACCAAAGAAGG[C/T]GCCTGGGAGGCCATG	84132
rs745421722	snp	C/T	1.77329e-05	0.0029776	synonymous-codon	USP42	GRCh38.p7	7:6149996	CAAATCCAAGCTGAA[C/T]TCCAGCGTGCTGGTG	84132
rs745441517	snp	A/C/T	3.47803e-05	0.00417003	missense	USP42	GRCh38.p7	7:6156986	GGCGTCGGACCTTTC[A/C/T]GTGAGAAAACGAAAC	84132
rs745449845	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6142317	CACCTCCTGGGTTCA[C/G]GCGATTCTTCTGCCT	84132
rs745456103	snp	C/T	6.12126e-05	0.00553196	synonymous-codon	USP42	GRCh38.p7	7:6154314	CGCTGAGCCTAGCCC[C/T]GGCGAGAGGGTCGAG	84132
rs745487904	snp	C/T	6.6368e-05	0.00576017	missense	USP42	GRCh38.p7	7:6142999	TTGATGGAGAAAACT[C/T]GTACAAGTGCAGCAA	84132
rs745489112	snp	A/G	1.66927e-05	0.00288895	missense	USP42	GRCh38.p7	7:6149602	CACCTCACTTAAATG[A/G]GACTGGACCATTGAA	84132
rs745502636	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6133799	CACTGGGATGACAGG[C/T]GTAAGCCACCGCACC	84132
rs745531431	in-del	-/AGG			upstream-variant-2KB	USP42	GRCh38.p7	7:6078047	TTGGGAGGCTGAGGC[-/AGG]AGAATTGCTTGAACC	84132
rs745547703	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6102588	CAACATAGCGAGCCC[A/G]TCTCTAAAAAAATAA	84132
rs745549973	snp	C/T	3.44525e-05	0.00415031	missense	USP42	GRCh38.p7	7:6153896	CGCCGCCCCGCGATC[C/T]CGGCACCCCCGCTAC	84132
rs745557502	snp	A/G	0.000413155	0.0143669	missense	USP42	GRCh38.p7	7:6153949	ATGGCCGTCGCCCCC[A/G]AGGAGCCTCCGCCCA	84132
rs745569983	snp	C/G/T	0.000254557	0.0112794	missense	USP42	GRCh38.p7	7:6154361	AAGCCCCAGGCCCTT[C/G/T]CCCAGCGAAGGAGAA	84132
rs745576966	snp	C/T	0.000154185	0.00877889	intron-variant	USP42	GRCh38.p7	7:6144050	TTGTGTGTATATATT[C/T]GTCTTCTTATACTTT	84132
rs745603542	in-del	-/AGAGAAGGC			intron-variant	USP42	GRCh38.p7	7:6160422	TCCACTCAGGAAGGC[-/AGAGAAGGC]AGAGTGATCTCCTCA	84132
rs745605892	snp	A/C/G	0.000103336	0.00718743	intron-variant	USP42	GRCh38.p7	7:6140867	GTAGTTGATGTTGCT[A/C/G]TAATGATTATACTTT	84132
rs745611614	snp	A/G	1.95907e-05	0.0031297	intron-variant	USP42	GRCh38.p7	7:6111097	TTCTCACCTGATGAA[A/G]CAAATACATACTTTT	84132
rs745611914	snp	C/T	3.45781e-05	0.00415787	intron-variant	USP42	GRCh38.p7	7:6147933	TTTTTATGTTAATTT[C/T]TAAAATGTAACTTCA	84132
rs745619695	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6150748	CTATTTCTCCTCCTG[C/T]GTGGCCACCTCTCTC	84132
rs745619719	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6159379	ATAGCCACTTAACGC[A/G]CACACACAGCAGAGG	84132
rs745644932	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6102421	CCAGATTCTACTAAG[A/C]TTTAAGGGGCAGCCT	84132
rs745712582	snp	C/T	1.69663e-05	0.00291253	missense	USP42	GRCh38.p7	7:6154993	GGAGACAACTGTAAC[C/T]TCTCTGATCGGTTTC	84132
rs745717287	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086184	GGGATTACAGGAGCC[C/T]GCCACCTCACCTGGC	84132
rs745730342	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6136454	CATTTTGAAACTTTA[A/G]AGCAAAAGATGACAA	84132
rs745731534	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6125431	GGAAGCGGGGGTTGC[A/T]GTGAGCCAAGAACAC	84132
rs745767979	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6141408	TGGGGTTTCACCTAT[C/T]GGCCAGGATGGTCTT	84132
rs745782080	snp	G/T	1.6799e-05	0.00289814	missense	USP42	GRCh38.p7	7:6150243	GGTGCCAGCTGCCAA[G/T]GCCAGCCTGCCCTGC	84132
rs745789379	snp	C/T	0.000139636	0.00835454	intron-variant	USP42	GRCh38.p7	7:6135994	TTTGTATTTATTACC[C/T]AGTTATACTTTTTTT	84132
rs745797090	in-del	-/TTATC			intron-variant	USP42	GRCh38.p7	7:6130166	ATGGATATTTTGGTG[-/TTATC]TTATAAGACACTGAG	84132
rs745800908	snp	A/G	1.77021e-05	0.00297502	synonymous-codon	USP42	GRCh38.p7	7:6154074	AAAGGGGATGATCGC[A/G]GAGGGCCCGCGGGAC	84132
rs745816513	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6089827	TGAGCTACCGCGCCC[A/G]GCCTCTTCACCTGAC	84132
rs745828349	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6133891	CCATGTTTCTTCTTC[-/T]TTTTTTTTTTTTTTT	84132
rs745838888	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6143719	ATAATTATTATTATT[A/T]TTAAATTAGATGAAT	84132
rs745872024	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6111695	GCAAGCTCTGCCTCC[A/C]GGGTTCAGGACATTT	84132
rs745888299	snp	C/T	0.000165615	0.00909836	missense	USP42	GRCh38.p7	7:6149833	TTCATAGTAATTCTT[C/T]GGAGAACCCTACCAA	84132
rs745899992	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6145767	TAAAATGTGAATACC[C/G]GAGGTAAAAATATTT	84132
rs745920123	snp	A/C	2.73856e-05	0.00370028	synonymous-codon	USP42	GRCh38.p7	7:6155194	CGAGACCGCGACTCC[A/C]GGTGAGCCTGGGGCC	84132
rs745987577	in-del	-/T	3.31538e-05	0.00407134	intron-variant	USP42	GRCh38.p7	7:6159428	CATCATTAAAATCTC[-/T]TTCCTGACCTTTGCT	84132
rs746008024	snp	A/G	2.2131e-05	0.00332641	missense	USP42	GRCh38.p7	7:6156764	TGCAGGCATCAGCAG[A/G]ACTCAGACCTCTCAG	84132
rs746044698	in-del	-/ACGGCG	5.54155e-05	0.00526352	cds-indel	USP42	GRCh38.p7	7:6154558	AGCACCACCCCGGCC[-/ACGGCG]ACGGCGACAGGCTCA	84132
rs746058415	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6134976	TTTATTTTTTGTAGA[G/T]ACAGGGTTTGACCAT	84132
rs746078856	snp	A/C	2.13641e-05	0.00326827	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111266	GCTGTGTCTTCATTG[A/C]ATGATGTGTCAAATC	84132
rs746080832	snp	A/G	1.87869e-05	0.00306482	synonymous-codon	USP42	GRCh38.p7	7:6154197	CGGGGACCACGCCCG[A/G]GACGCTCAGGACCCA	84132
rs746086008	snp	A/G	1.65987e-05	0.00288082	intron-variant	USP42	GRCh38.p7	7:6150538	TCTGAGGCACGTGTG[A/G]CAGCATAGTAGGAAA	84132
rs746090816	snp	A/T	0.0012981	0.0254433	intron-variant	USP42	GRCh38.p7	7:6140242	TACACACATGTGGTT[A/T]AAAAATGGTAATAGT	84132
rs746096062	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6108040	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCACG	84132
rs746102143	in-del	-/TTTTTTTTTTTT			intron-variant	USP42	GRCh38.p7	7:6082605	TTTCTTTCTTTCTGT[-/TTTTTTTTTTTT]TTTTTTTTTTTTGAG	84132
rs746105646	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6100433	CTCCTGGGTTCAAGC[A/G]ATTCTCTTGCCTCAG	84132
rs746124941	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6102270	CAGGTGCCATCACCA[A/C]AGCCAACTGATTTTT	84132
rs746152213	snp	G/T	1.65899e-05	0.00288005	intron-variant	USP42	GRCh38.p7	7:6140085	ACAGCATCTGGAGTT[G/T]TTGCAAAGCTCTTCT	84132
rs746197290	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6139801	TGCCTTTTCCGCCTC[C/T]GCTCCCTTTCCTCCC	84132
rs746201590	snp	A/C	1.67657e-05	0.00289527	missense	USP42	GRCh38.p7	7:6147777	GTGAACTTACTCATC[A/C]CACCCATAGCCCCGG	84132
rs746223298	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138969	ATGTTAGTGCTATTT[C/T]CTCATAAAGTAAGTA	84132
rs746269890	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6116311	TGAGAACTTCATCTT[C/T]AACCTACATGGCAGG	84132
rs746288421	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6118319	TTGAGTTCAGTAGTT[G/T]GAGACCAGTTTGGGC	84132
rs746290314	snp	A/G	2.19132e-05	0.00331001	intron-variant	USP42	GRCh38.p7	7:6157060	GTATGGCCAGGGTAA[A/G]AGGAGATACTTGGAA	84132
rs746306147	snp	C/T	5.4308e-05	0.00521067	synonymous-codon	USP42	GRCh38.p7	7:6154680	CACCGAGGGCGAGCG[C/T]GGCTGGGGCCGGGAG	84132
rs746334252	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6078905	TAGTAGATCCTGTCA[A/G]TTAAGAGCGAATTGC	84132
rs746348025	in-del	-/GTGT			intron-variant	USP42	GRCh38.p7	7:6153730	CCCACGCTAACGGGC[-/GTGT]GTGTTTGTTTGTTTG	84132
rs746348129	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126536	GTGATCTGCCCGCCT[C/T]AGCCTCCCAAAGTGC	84132
rs746370770	snp	A/C/G	0.000436149	0.0147611	missense	USP42	GRCh38.p7	7:6150072	GGGCTGGGCAAGGAG[A/C/G]ATGGGATTGGTACGA	84132
rs746382464	snp	C/G/T			intron-variant	USP42	GRCh38.p7	7:6148865	AGAGTGACATCAGGA[C/G/T]TCTGGCAAACAGGAG	84132
rs746390049	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095265	GATCCCTTAGCAATA[A/G]GGGAACCCTGAGGGT	84132
rs746391477	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094072	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	84132
rs746398286	snp	C/G	1.81171e-05	0.00300969	missense	USP42	GRCh38.p7	7:6154126	GAAGGGTTGAGTCCG[C/G]CTCCGCCTGCGCGGT	84132
rs746466418	in-del	-/T/TT			intron-variant	USP42	GRCh38.p7	7:6092041	TTCTTCTTCTTCTTC[-/T/TT]TTCTTCTTCTTCTTT	84132
rs746488006	snp	C/T	3.31543e-05	0.00407137	missense	USP42	GRCh38.p7	7:6142975	AGCAGTTTGTGAAGC[C/T]GGAACAGCTTGATGG	84132
rs746524745	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6098183	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	84132
rs746537466	snp	G/T	4.19331e-05	0.00457873	missense	USP42	GRCh38.p7	7:6156779	GACTCAGACCTCTCA[G/T]CAGCGTGCTCTGACG	84132
rs746549918	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096765	ACAGCCTGTCTTGCC[C/T]TGTGTTTTATTAGCC	84132
rs746559038	snp	C/T	5.76319e-05	0.00536774	missense	USP42	GRCh38.p7	7:6154307	AAGGGGACGCTGAGC[C/T]TAGCCCCGGCGAGAG	84132
rs746571466	snp	A/G	0.000139441	0.00834871	missense	USP42	GRCh38.p7	7:6153857	CAGATGCGGCCGCCG[A/G]CCTCAGCAGCACCAA	84132
rs746592691	in-del	-/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077642	AGGCAGGCAGATCAC[-/T]TGTAGGTCAGGAGTT	84132
rs746597902	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6132732	GCTGGAGTGCAGCGT[C/G]GAGATCTCGGCTCAC	84132
rs746622044	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6086759	GAGATGGAGTTTCGC[G/T]CTTGTCGCCCAGGCT	84132
rs746645842	in-del	-/TTTTTTTTTTTTT			intron-variant	USP42	GRCh38.p7	7:6082604	TTTTCTTTCTTTCTG[-/TTTTTTTTTTTTT]TTTTTTTTTTTTGAG	84132
rs746655295	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6115629	AGTGCTATGATTACT[-/A]AGAAGTTGGTTTATT	84132
rs746656434	snp	A/G	5.09515e-05	0.00504709	intron-variant	USP42	GRCh38.p7	7:6142888	GACCCAAACACAAGT[A/G]ACGGTGTGCGGTGAT	84132
rs746660207	snp	C/G/T	3.3161e-05	0.00407181	missense	USP42	GRCh38.p7	7:6147858	AGGCTGCGCCAGGCT[C/G/T]TATCGGACCACAGCT	84132
rs746663884	snp	G/T	5.16205e-05	0.00508011	synonymous-codon	USP42	GRCh38.p7	7:6150293	TAAGGCAAACGGTCT[G/T]CCTGGAAAGGTGAGT	84132
rs746672727	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6123951	CATGATCTTGGCTCA[C/G]TGGAAACTCTGCCTC	84132
rs746675172	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6085539	ATAGATTATATAGAA[G/T]AGGGACCTGCTGTAT	84132
rs746680308	snp	A/G	1.69758e-05	0.00291335	intron-variant	USP42	GRCh38.p7	7:6147913	AGTCCTTAGGGAGAA[A/G]AACATTTTTATGTTA	84132
rs746698714	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115141	TGGAGAAACCAGATC[A/G]TTGAAAATTTCTCAT	84132
rs746702875	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6157618	AGCCAGGATGGTCTC[A/G]AGAACTCTTGGTTTT	84132
rs746761179	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6142406	TATTTTTAGTAGAGA[C/T]GGGGTTTTACCATGT	84132
rs746761287	snp	G/T	4.65604e-05	0.00482473	intron-variant	USP42	GRCh38.p7	7:6135977	ACTATTGTAGTTTTA[G/T]ATTTGTATTTATTAC	84132
rs746793140	snp	C/T			utr-variant-3-prime	USP42	GRCh38.p7	7:6160709	ACCTTTTCTTAATTA[C/T]CCTTATTCCGAATGG	84132
rs746798598	snp	A/G	0.000132593	0.00814119	utr-variant-3-prime, intron-variant	USP42	GRCh38.p7	7:6159484	CAAAACAAAAAATTC[A/G]CTAGTTATGGTAAGC	84132
rs746814155	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6151695	TCATCCACCCGCTGT[C/G]GCCTCCCAAAGGGCT	84132
rs746860102	snp	C/T	1.6755e-05	0.00289435	synonymous-codon	USP42	GRCh38.p7	7:6150224	AAACGGCCTAGCGCC[C/T]GATGGTGCCAGCTGC	84132
rs746868233	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126929	AGTTGCATATTTGAT[C/T]TTATAAGAAACTGCC	84132
rs746870925	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6102833	ATAGAATGCTCAGAG[-/T]GGGGGAGTCAAGTGA	84132
rs746891100	snp	A/C/G	3.59986e-05	0.00424243	synonymous-codon	USP42	GRCh38.p7	7:6153984	CGGCGAGGACATCGT[A/C/G]GGGGACACAGCACCC	84132
rs746896177	in-del	-/AA			upstream-variant-2KB	USP42	GRCh38.p7	7:6078603	CAAGACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA	84132
rs746912424	snp	C/G	3.31241e-05	0.00406952	missense	USP42	GRCh38.p7	7:6145528	TAGGATGTGAAATAC[C/G]CTGAGTATCTTGATA	84132
rs746944339	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6108989	TGTGAATAAGAACAT[C/G]GTAGAGAACAGCAAG	84132
rs746972693	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6101175	AGCCTCAGGAGAAGA[A/G]GCAGCTGTGAGTTAT	84132
rs746991934	snp	A/T	1.76855e-05	0.00297362	synonymous-codon	USP42	GRCh38.p7	7:6135887	AATGCAAGCACATAT[A/T]ACCCAGGCACTCAGT	84132
rs747000461	snp	C/T	2.01696e-05	0.0031756	intron-variant	USP42	GRCh38.p7	7:6145662	CTACATAAAAGTAAG[C/T]TGTGCAGATTTGCTA	84132
rs747001372	snp	A/C/T	3.53971e-05	0.00420685	missense, synonymous-codon	USP42	GRCh38.p7	7:6154024	TGTGATCCCGGGAGC[A/C/T]TAACAGGCGATGCGA	84132
rs747020183	snp	C/G	4.19489e-05	0.0045796	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111241	GGATGCAGGTTCTGC[C/G]AGCTGGGGTGCTGTG	84132
rs747042880	in-del	-/AAG	5.38295e-05	0.00518766	cds-indel	USP42	GRCh38.p7	7:6154467	AGAGAGAGCAGGAGC[-/AAG]AAGACTGAGGGCCAC	84132
rs747061236	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6146796	CAGCTGCAGGGAGAG[A/G]TGGTGGCTGACAAGG	84132
rs747103141	snp	A/G	4.07814e-05	0.00451542	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111364	AAAACCATCACCACA[A/G]AAGGATCAAGGTACT	84132
rs747126672	snp	C/G	3.465e-05	0.00416219	missense	USP42	GRCh38.p7	7:6155086	CATGTTGAAAAGAAA[C/G]CCCGGAGGAGCGAAC	84132
rs747135308	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6113234	TGGGGGTGGGTGTTG[C/T]AGTTTGGCTTGCTGA	84132
rs747137240	snp	C/T	4.96841e-05	0.00498393	synonymous-codon	USP42	GRCh38.p7	7:6149651	CATGTCGAGTCCTAA[C/T]GGGAATTCCAGTGTC	84132
rs747150685	in-del	-/A	0.000449367	0.0149827	intron-variant	USP42	GRCh38.p7	7:6140241	TACACACATGTGGTT[-/A]AAAAAATGGTAATAG	84132
rs747173263	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6097713	CTCCTGCCTCAGCCT[-/C]CCGAGTTGCTGTGAC	84132
rs747177107	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6110869	GGGCATGAAATGAAA[A/G]TGAGAAGTTCTTTTA	84132
rs747191141	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077966	TGGGCGTGAGCCACC[A/G]GGCCTGGCCCTTAAA	84132
rs747194215	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6088282	CTTTTTGCGACGGAG[A/T]CTTGATCTGTCACCC	84132
rs747197429	snp	C/G/T	0.000108457	0.00736334	missense	USP42	GRCh38.p7	7:6154123	CCGGAAGGGTTGAGT[C/G/T]CGGCTCCGCCTGCGC	84132
rs747205983	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6113008	TGCTGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC	84132
rs747225916	snp	C/T	1.78777e-05	0.00298974	intron-variant	USP42	GRCh38.p7	7:6147713	GTGTCCTGTGTCACC[C/T]TAAGTATCGCTCTCC	84132
rs747226108	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137436	CGATCTTGGCTCACT[A/G]CAACCTCTGCCTCTC	84132
rs747239586	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6102504	TGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	84132
rs747245593	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6086319	CACGCCATTCTCCTG[A/C]CTCAGCCTCCAGAGT	84132
rs747268040	snp	C/T	1.65963e-05	0.0028806	intron-variant	USP42	GRCh38.p7	7:6150401	CTGAAATATTTTTGT[C/T]TTTATTGCAGTTGAT	84132
rs747327964	snp	A/G	8.71396e-05	0.00660017	synonymous-codon	USP42	GRCh38.p7	7:6146210	CAGTGATATTAGATC[A/G]GTACTCAGCCAACAA	84132
rs747342740	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6130530	CATGATTGTCACAAC[A/G]TGGGGTGGGACAGGG	84132
rs747402561	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6129775	CTGAGGCAAGAGAAT[A/C]ACTTGAACCCAGGAG	84132
rs747404032	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6143205	TTCTGCAAGATGCGC[-/A]GCTCTGTGCCTGTGA	84132
rs747444305	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6140696	TCTAAGAGGGTATAC[C/G]AGTTTTGATTCTAAT	84132
rs747459546	snp	C/T	9.92014e-05	0.00704208	missense	USP42	GRCh38.p7	7:6153886	AAGAAGGCTCCGCCG[C/T]CCCGCGATCCCGGCA	84132
rs747473136	snp	C/G	5.24907e-05	0.00512275	missense	USP42	GRCh38.p7	7:6154667	TCAGACACCACTACA[C/G]CGAGGGCGAGCGTGG	84132
rs747479991	snp	C/G	1.72931e-05	0.00294045	synonymous-codon	USP42	GRCh38.p7	7:6149981	GCCCGTGATGAATGG[C/G]AAATCCAAGCTGAAC	84132
rs747492566	snp	A/C	0.000952582	0.0218033	missense	USP42	GRCh38.p7	7:6154615	AGGTGCAGTCACCAC[A/C]ACTCCCGACACCGGA	84132
rs747510996	snp	A/G	1.73794e-05	0.00294778	intron-variant	USP42	GRCh38.p7	7:6116767	CAGAATTAACGTTCT[A/G]TTTGCCCTCATTTTC	84132
rs747536571	snp	C/T	1.69252e-05	0.00290901	intron-variant	USP42	GRCh38.p7	7:6115529	TCCAAAACATGTAAG[C/T]GTTCCGTGTTGTGTT	84132
rs747549188	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152255	ATACTCGGTGCCAGG[C/T]GCGGGTTCATCATCA	84132
rs747569062	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6146334	TTCAATATTCAGTGT[-/T]TTTAAAAAAAAAAAA	84132
rs747585209	snp	A/G			intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6121614	TTCAGCAGTGAAGCC[A/G]TCTGGACCTTGCAGT	84132
rs747626367	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6116472	CATTCTTTATAAATG[C/T]AGTCTCCCTGTTCTT	84132
rs747667261	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086850	CCTACCTCAGCCTCC[C/T]GAGTAGCTGGAATTA	84132
rs747701032	snp	C/G	0.000126382	0.00794828	synonymous-codon	USP42	GRCh38.p7	7:6154920	CCGCGCAGGCGCGCC[C/G]CACGCCCTCGCCCCG	84132
rs747702121	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6083216	AGGCGTGAGCCACCG[C/T]ACCCAGCTTATTTAT	84132
rs747703274	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6158168	GTGAAATTCAGACCT[C/T]AGTGTCTGTGGCTTG	84132
rs747715423	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6124125	AGGTCATCTGCCTGC[C/T]TCAGTCTCCCTAAGT	84132
rs747722182	in-del	-/TG			intron-variant	USP42	GRCh38.p7	7:6138063	AAAATGTCATTGCTC[-/TG]TGTGTGTGTGTATCC	84132
rs747735804	snp	G/T	4.97211e-05	0.00498579	utr-variant-3-prime, intron-variant	USP42	GRCh38.p7	7:6159468	ATTGAAAACTCAGCC[G/T]CAAAACAAAAAATTC	84132
rs747741283	snp	A/G	1.8757e-05	0.00306237	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6135852	TCAGGTCATGCAGAA[A/G]GCTTTTGTATGATGT	84132
rs747753876	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6120449	GGTTTCACAGTGTTG[G/T]CCAGGCTGGTCTCAA	84132
rs747778085	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6117551	TTCATTTCTCTTAGG[C/T]AAATATCTAGGAGTA	84132
rs747785779	snp	A/G	1.77059e-05	0.00297533	missense	USP42	GRCh38.p7	7:6154022	TGTGTGATCCCGGGA[A/G]CTTAACAGGCGATGC	84132
rs747787085	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095408	GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	84132
rs747803080	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6118679	TGATGTGAAGATGGA[A/G]CAAGTTTATTTTTTT	84132
rs747842497	snp	C/T	6.70017e-05	0.0057876	missense	USP42	GRCh38.p7	7:6150220	AAGAAAACGGCCTAG[C/T]GCCTGATGGTGCCAG	84132
rs747853552	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6144646	AGGCCTAGTTGGGCA[C/T]ATCACTTCAAGCCGG	84132
rs747859738	snp	C/T	0.000149131	0.00863385	intron-variant	USP42	GRCh38.p7	7:6145508	CTCCTGTTTCCATTT[C/T]CTTCTAGGATGTGAA	84132
rs747905300	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6132846	CCGGCTAATTTTTTT[C/G]TATTTTTAGTAGAGA	84132
rs747907633	snp	A/G	1.7386e-05	0.00294834	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116899	GACAGCAAGAGAGAG[A/G]ACCAAGACAAAATTC	84132
rs747931138	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6109934	TCAAACGCCTGACCT[A/C]AGGTGATTCACCTGC	84132
rs747984591	snp	C/T	3.62358e-05	0.00425636	synonymous-codon	USP42	GRCh38.p7	7:6153978	CAGCGCCGGCGAGGA[C/T]ATCGTGGGGGACACA	84132
rs748018064	snp	C/T	4.42351e-05	0.00470272	intron-variant	USP42	GRCh38.p7	7:6157097	AGATAGAAACTATTT[C/T]TTAATACATTTTCTT	84132
rs748019396	snp	A/G	8.46991e-05	0.0065071	missense	USP42	GRCh38.p7	7:6154370	GCCCTTCCCCAGCGA[A/G]GGAGAAAATCGGCAG	84132
rs748022693	in-del	-/TTTTA			intron-variant	USP42	GRCh38.p7	7:6157379	CTTGGTTTGGTTTGG[-/TTTTA]TTTTATTTTATTTTA	84132
rs748026598	in-del	-/GCACGAGCGGGCCGGGCT	0.000162575	0.0090145	cds-indel	USP42	GRCh38.p7	7:6154800	CCACGGCGGCCGCGA[-/GCACGAGCGGGCCGGGCT]GCACGAGCGGCCGCA	84132
rs748030072	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6157662	TAGAAATACTTTTGC[A/G]GCGTATACGTTACTC	84132
rs748035596	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081574	GGGGGCGGAGCCCGC[C/T]GCAGACCCCGCCCCT	84132
rs748041339	in-del	-/TCCC			intron-variant	USP42	GRCh38.p7	7:6126073	CCAAGCCCACTTGTG[-/TCCC]TCCCTGCCTTCCCCT	84132
rs748071198	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6133703	TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTTTC	84132
rs748073679	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6100112	CCGGCCTCAGCCTCC[C/T]AAAGTGCTGGGATTA	84132
rs748105598	snp	A/C/G	0.00165386	0.0287105	intron-variant	USP42	GRCh38.p7	7:6139211	TAAGTACAACAGAGC[A/C/G]CCAGCCATGTCTTCA	84132
rs748115231	snp	C/G	0.000103354	0.00718792	synonymous-codon	USP42	GRCh38.p7	7:6154443	GCGCTCGTCCAGCGG[C/G]GAGCCCGCCAGAGAG	84132
rs748115834	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6127195	GTTGTTGTACTGTCA[A/G]GTTTTGAGGATATGT	84132
rs748143474	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6156042	CACCTCACCTGGCCT[A/G]TTTTTGTATTTTTAA	84132
rs748175107	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103588	GACAGTGGCGCACCG[C/G]TGGGGTCAGGCGGAC	84132
rs748198567	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6138817	GCCTGATGATCTGAG[A/C]TGGAACAATTTCATC	84132
rs748213961	snp	C/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114925	TCGATCTCCTGACCT[C/G]ATAATCCGCCTGCCT	84132
rs748237144	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6091224	CTTTTCTCTTCTCTT[C/G]TCTTTTCTTTTCTTT	84132
rs748240259	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6137630	CCCAAAGTGCAGAGA[C/T]TACAGACGTGAGCCA	84132
rs748285932	snp	C/T	1.78992e-05	0.00299153	missense	USP42	GRCh38.p7	7:6154109	CGTTGGCGGAAGCCC[C/T]GGAAGGGTTGAGTCC	84132
rs748287245	in-del	-/TGT			downstream-variant-500B, cds-indel	CYTH3, USP42	GRCh38.p7	7:6161445	GGTTTATACAGTTTG[-/TGT]TGTTCAGAGATGTTT	84132
rs748287854	snp	G/T	1.74208e-05	0.00295129	intron-variant	USP42	GRCh38.p7	7:6150326	ACGTCAGGGTCTTCA[G/T]CCTCGTTTGTGGCGG	84132
rs748290020	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6102801	CTAGCTAAGGAATTT[A/G]GACTTTGCTGTGAGC	84132
rs748293416	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6125213	AAAAAAACAGGCAGG[A/T]TGCAGTGGCTCATGC	84132
rs748296832	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6088641	GATTGACGTCACTAC[A/G]CCAGTGATAGCGTCT	84132
rs748335879	snp	A/G	6.8355e-05	0.00584575	intron-variant	USP42	GRCh38.p7	7:6145684	GATTTGCTATTAACT[A/G]TTGTTACATACATGC	84132
rs748346918	in-del	-/CTATT			intron-variant	USP42	GRCh38.p7	7:6145903	GGTGAAACCCCGCCT[-/CTATT]AAAAATACAAAAATT	84132
rs748347563	snp	A/T	7.17643e-05	0.00598974	missense	USP42	GRCh38.p7	7:6154603	CGCTCTCTGGGCAGG[A/T]GCAGTCACCACCACT	84132
rs748350945	snp	A/G	0.00023597	0.0108595	synonymous-codon	USP42	GRCh38.p7	7:6154644	GAGCGGGGTGGAGCT[A/G]GACTGGGTCAGACAC	84132
rs748363893	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077237	TGACCACAGCTCTTA[C/T]GCACCCTGTATATAG	84132
rs748384636	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152451	CACCTGTGGGGGTGC[C/T]GTTCATGCTGGCGGG	84132
rs748399274	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6119412	GGAGGTGGTGACTGC[A/G]GTGAGCCATTATTGT	84132
rs748410824	snp	C/G/T	3.54819e-05	0.00421188	missense	USP42	GRCh38.p7	7:6154082	TGATCGCGGAGGGCC[C/G/T]GCGGGACTCGGCGTT	84132
rs748443022	snp	A/G	1.65282e-05	0.00287469	synonymous-codon	USP42	GRCh38.p7	7:6156784	AGACCTCTCAGCAGC[A/G]TGCTCTGACGCTGAC	84132
rs748456052	snp	A/G	2.3729e-05	0.00344441	intron-variant	USP42	GRCh38.p7	7:6135999	ATTTATTACCTAGTT[A/G]TACTTTTTTTTTTTT	84132
rs748460743	snp	A/T	1.65844e-05	0.00287957	missense	USP42	GRCh38.p7	7:6149919	TCTACGATGTCAGTT[A/T]CTAGTAAAGTAACAA	84132
rs748478544	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6122560	ACTGCAACCTGCGCC[C/T]CATGGGTTCAAGCGA	84132
rs748480073	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6147120	ATTGAAATATTAAAC[A/G]CTGGCATTGGATTTC	84132
rs748480302	snp	A/G	1.65688e-05	0.00287821	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6115480	TTTAACCTACACACC[A/G]CCTCTTGCCAATTAC	84132
rs748505571	in-del	-/CTT			intron-variant	USP42	GRCh38.p7	7:6092126	TTCTTCCTCTTCCTT[-/CTT]CTTCTTCTTCTTCTT	84132
rs748518510	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6121813	AGAGGTGTGCATCAC[C/T]ACACACAGCTAATTT	84132
rs748537946	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6096607	TTCCATCCAAGGTTT[A/G]GGGAAGAACAGGTGC	84132
rs748562166	in-del	-/AGTGC			intron-variant	USP42	GRCh38.p7	7:6093336	TGTTGCCCAGGCTGG[-/AGTGC]AGTGGCAGGATTTCA	84132
rs748566848	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6131723	ACCCCAGGAAACTCA[C/G]CACCATGTCTTCCTT	84132
rs748588143	snp	C/T	3.09478e-05	0.00393356	missense	USP42	GRCh38.p7	7:6154256	CAGAGCGGCCGCCAG[C/T]TCCTGTGCTGGACAT	84132
rs748599991	snp	A/G			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161655	TTAAAACCTTCAAGT[A/G]AGTGCTCCTGCCGAA	84132
rs748606518	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6111088	AGATTGCTTTTCTCA[C/T]CTGATGAAACAAATA	84132
rs748615868	in-del	-/A	3.31625e-05	0.00407188	intron-variant	USP42	GRCh38.p7	7:6140090	ATCTGGAGTTTTTGC[-/A]AAGCTCTTCTCTCAT	84132
rs748637649	snp	A/C	3.55935e-05	0.00421847	intron-variant	USP42	GRCh38.p7	7:6141029	ATTTTTAAAATAAGT[A/C]ATTTTATGTAACTGT	84132
rs748638149	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6113297	AAACACAACCTAATC[A/G]AATGTTGCACATGGA	84132
rs748647729	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6147982	TAGTGGTTGCTGTGT[C/T]CTCAAATACATCTGA	84132
rs748664352	in-del	-/A			utr-variant-3-prime	USP42	GRCh38.p7	7:6160772	AAATACCGTGTATAT[-/A]AATCCCATTGAAATA	84132
rs748674981	snp	G/T	0.00148002	0.0271628	missense	USP42	GRCh38.p7	7:6153807	CGACGCCGAGCCTCA[G/T]CCTGGCAGCCCCGCC	84132
rs748757953	snp	G/T	1.7736e-05	0.00297787	intron-variant	USP42	GRCh38.p7	7:6147724	CACCCTAAGTATCGC[G/T]CTCCTTGTTTCCAGG	84132
rs748766163	in-del	-/TT			intron-variant	USP42	GRCh38.p7	7:6093586	TCTCTTTCTTTTCTC[-/TT]TTTTTTCTTTCTTTC	84132
rs748779106	snp	C/G/T	1.78191e-05	0.00298484	missense, synonymous-codon	USP42	GRCh38.p7	7:6150143	GGAGGCCACTCCGCA[C/G/T]GAGCTTCAAGAACCC	84132
rs748796953	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6107280	GTCATTTGTTAGTGA[C/T]TGTTCTGAAGGTATG	84132
rs748800904	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6118272	AGGTGTGGTGGTTCA[C/T]GTGTTTTGGGAGGCT	84132
rs748811904	snp	C/G/T	2.88713e-05	0.00379932	intron-variant	USP42	GRCh38.p7	7:6157077	GGAGATACTTGGAAT[C/G/T]AGGAAGATAGAAACT	84132
rs748819055	snp	G/T	1.6574e-05	0.00287867	utr-variant-3-prime, intron-variant	USP42	GRCh38.p7	7:6159462	TAGGTGATTGAAAAC[G/T]CAGCCTCAAAACAAA	84132
rs748854085	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6117595	CTGGGGTGGGTGTGT[A/T]CTTTAACATTTTAAG	84132
rs748859633	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6141868	CATTATTTTTAACAG[C/T]TTGATATGTACTGCT	84132
rs748877135	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6125891	TTATTTGTGGTAACT[A/G]GATTCACATGCACTT	84132
rs748899664	snp	G/T	4.70245e-05	0.00484872	missense	USP42	GRCh38.p7	7:6154729	CCGCGCTGGGACAGG[G/T]GCCGGTACTACCATG	84132
rs748904301	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130635	GTGCCTTGCTACAGC[C/T]TGTTGAGTGTAAGTC	84132
rs748930740	snp	A/G	6.9512e-05	0.00589501	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116798	TCCCTTTCTCAGTCC[A/G]TAATTCATTCCCCAC	84132
rs748952419	snp	C/G	3.97939e-05	0.00446042	missense	USP42	GRCh38.p7	7:6150082	AGGAGAATGGGATTG[C/G]TACGATTGTGAGCTC	84132
rs748958467	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6108201	CAAAACATAACAAAA[C/G]AAACAAACAAAAAAA	84132
rs748976441	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6134816	TTTGAGACAGGGTCT[C/T]GCTCTGTTGCCCAGG	84132
rs748983897	snp	C/T	8.68938e-05	0.00659085	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116869	GTGTGGATGAAAACC[C/T]AGCACTAGCACCTGG	84132
rs749056836	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6158392	TCCCCTCCTCCCAGG[G/T]GCTTTTGACGAATCT	84132
rs749067274	snp	C/G	2.82985e-05	0.00376145	intron-variant	USP42	GRCh38.p7	7:6144056	GTATATATTCGTCTT[C/G]TTATACTTTTGTTTC	84132
rs749081139	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6100266	TAGTCCCCCTAGATG[G/T]GCGCCTGATACTGTT	84132
rs749119718	snp	A/G	1.69456e-05	0.00291075	synonymous-codon	USP42	GRCh38.p7	7:6154365	CCCAGGCCCTTCCCC[A/G]GCGAAGGAGAAAATC	84132
rs749143956	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6111470	CTTATTTTGCAAGGC[A/G]TGAGGCCACCTGAGT	84132
rs749152395	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6081866	TTACCAGCTGAGTTT[C/T]CTGACTTTTATATTC	84132
rs749166555	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6129860	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	84132
rs749221442	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6158414	GACGAATCTTCAGGG[A/C]TGCCCTGAGGCCTTT	84132
rs749224092	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6101160	CCTTCAGCTAAGAAC[A/G]GCCTCAGGAGAAGAG	84132
rs749226025	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086916	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	84132
rs749239250	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6158683	GCGGGCCTTGTAGAC[A/G]TTCTGGACATTTCAG	84132
rs749248742	snp	C/T	1.70892e-05	0.00292306	synonymous-codon	USP42	GRCh38.p7	7:6155073	GAACAGTGACAGTCA[C/T]GTTGAAAAGAAAGCC	84132
rs749259808	snp	A/T	1.65688e-05	0.00287821	missense	USP42	GRCh38.p7	7:6149631	AAAGACACGCCAAGC[A/T]GTTCCATGTCGAGTC	84132
rs749266082	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6084040	TTTTTGTTTTGTTTT[C/G]TTTTGAGACAGAGTC	84132
rs749312422	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6129092	GCTGGGATTACAGGC[A/G]TGTGCCACTGGGCCT	84132
rs749343457	snp	A/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161924	GGGAGTATATACATC[A/T]TTGAATAACAGACAC	84132
rs749451518	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6105626	CTGCTCCGTGGAGAG[A/T]CCGAGGTGCCCACGC	84132
rs749484476	snp	C/T	3.31461e-05	0.00407086	missense	USP42	GRCh38.p7	7:6149908	CCTCGAACGCATCTA[C/T]GATGTCAGTTTCTAG	84132
rs749487250	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6144768	CTAGCTACTCGGGAG[A/G]CTGAGGCAGGAGAAT	84132
rs749488498	in-del	-/CTGT	0.000116048	0.00761646	intron-variant	USP42	GRCh38.p7	7:6159506	TGGTAAGCTGTTTTC[-/CTGT]CTGTCTGTTTCCTCA	84132
rs749490494	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6110045	CACCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC	84132
rs749499171	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6128596	GTGTCTTTTAACTCT[A/C]TGCTGCTCTAGGCTG	84132
rs749503707	snp	A/G	3.95312e-05	0.00444567	missense	USP42	GRCh38.p7	7:6153835	GCCGCCGAATCCCTG[A/G]AGGAGCCAGATGCGG	84132
rs749533890	snp	A/G			utr-variant-5-prime	USP42	GRCh38.p7	7:6078749	GTAAGTCCCAGATAC[A/G]AAGGCACTTGTCAGG	84132
rs749539831	snp	C/G	0.000175824	0.0093745	missense	USP42	GRCh38.p7	7:6154538	GCCAGGACCGCCACG[C/G]CCCGGAGCACCACCC	84132
rs749580241	snp	C/T	2.07734e-05	0.00322277	intron-variant	USP42	GRCh38.p7	7:6111402	AAAAGAGAGAATTAC[C/T]GCCAGAAACTCCTGT	84132
rs749593344	snp	A/C	1.72368e-05	0.00293566	intron-variant	USP42	GRCh38.p7	7:6141009	ATAATTATGGGAGTA[A/C]TTACATTTTTAAAAT	84132
rs749609264	in-del	-/AAG	0.000756879	0.0194388	cds-indel	USP42	GRCh38.p7	7:6156818	CACAGACACAAAAAA[-/AAG]AAGAAGAAAAAGAAG	84132
rs749621713	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6148074	CGAGCGCAGTGGCTC[A/C]AGCTTGTAATCCCAG	84132
rs749633309	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6085519	AGTTAACATGTATAA[C/G]TCATATAGATTATAT	84132
rs749668630	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6157586	TGTTTTTAGTAGAGA[C/T]GGTGTTTCACCGTGT	84132
rs749674543	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136047	TCTTGCTCTGTCGCC[C/T]AGGCTGGAATGTAGT	84132
rs749679130	snp	C/T	1.65671e-05	0.00287807	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115339	CCTAGGTGATGGCAT[C/T]GCTCCTCCACAGAAA	84132
rs749697938	snp	A/G	1.66062e-05	0.00288146	intron-variant	USP42	GRCh38.p7	7:6150545	CACGTGTGGCAGCAT[A/G]GTAGGAAATCCAGTA	84132
rs749704861	snp	C/T	0.000152917	0.00874271	synonymous-codon	USP42	GRCh38.p7	7:6154788	CTGGAAGCCCTTCCA[C/T]GGCGGCCGCGAGCAC	84132
rs749724749	snp	A/C/G	0.000342129	0.0130755	intron-variant	USP42	GRCh38.p7	7:6155221	GGCCTTGTGCTCCCC[A/C/G]AGGCGCTGGCGCTGC	84132
rs749750963	in-del	-/AATTGTAATCA			intron-variant	USP42	GRCh38.p7	7:6090971	TTAGGGATCAATTTC[-/AATTGTAATCA]ATCACAGTTACAATC	84132
rs749790320	in-del	-/TT/TTTTT			intron-variant	USP42	GRCh38.p7	7:6092035	TTCTTCTTCTTCTTC[-/TT/TTTTT]TTCTTCTTCTTCTTC	84132
rs749794022	snp	A/C			utr-variant-3-prime	USP42	GRCh38.p7	7:6161082	TGTATTTTATAGACA[A/C]GTTCTGTTTTTGAAC	84132
rs749802236	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6089016	CCTGCACTGGGGTTT[A/C]TTTTCTATATTTATT	84132
rs749823473	snp	A/G	5.63587e-05	0.00530812	missense	USP42	GRCh38.p7	7:6154201	GACCACGCCCGGGAC[A/G]CTCAGGACCCATCCC	84132
rs749832963	snp	G/T	1.6563e-05	0.00287771	missense	USP42	GRCh38.p7	7:6149804	TGTTCGCCAGTGTCA[G/T]TCTCAACCTAACCTT	84132
rs749866923	snp	C/T	2.12307e-05	0.00325806	intron-variant	USP42	GRCh38.p7	7:6144200	AAAATTGCTAAGGTA[C/T]GTGGATGATGTCATT	84132
rs749900101	in-del	-/A	1.68562e-05	0.00290307	intron-variant	USP42	GRCh38.p7	7:6147904	AAGGTAACAGTCCTT[-/A]AGGGAGAAGAACATT	84132
rs749902965	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152909	TCAGAGAAAGGGAGT[C/T]GAGAGGAAAGGAGGA	84132
rs749910009	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077121	CTTGTGATCTGCCCA[C/T]CTCAGCCTCCCAAAG	84132
rs749947122	snp	C/T	0.000179921	0.00948304	missense	USP42	GRCh38.p7	7:6154414	GACCGAGGCCACTAC[C/T]GCAGCCGGAGAGAGC	84132
rs749954748	snp	A/G	1.66004e-05	0.00288096	intron-variant	USP42	GRCh38.p7	7:6145483	ATGATCTGTGCCCTC[A/G]GAAATGTTTCTCCTG	84132
rs749955153	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6127658	ACCACTCTACACAAG[G/T]CCTTGTTACTGTAGT	84132
rs749955992	snp	A/G			downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161512	AGCACTTGCCCCACT[A/G]TAAATATACAGCATG	84132
rs749985752	in-del	-/TCTCTTTTTTTTTTTTTTGAGATGGAG			intron-variant	USP42	GRCh38.p7	7:6089533	TGCTTCACCTGACTT[-/TCTCTTTTTTTTTTTTTTGAGATGGAG]TCTCACCCTGTCTCC	84132
rs750003222	in-del	-/T	2.70746e-05	0.00367921	intron-variant	USP42	GRCh38.p7	7:6135963	GGCGTAAGTATTAAC[-/T]TATTGTAGTTTTATA	84132
rs750004652	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104358	GAATGCTGGGATTAA[C/G]GCGTGAGCCACCGCG	84132
rs750005972	snp	C/T	0.000497995	0.0157718	synonymous-codon	USP42	GRCh38.p7	7:6147757	CCATGATGTGAAAAA[C/T]GGAGGTGAACTTACT	84132
rs750030997	in-del	-/TCT			intron-variant	USP42	GRCh38.p7	7:6092101	TCTTCTTCTTCCTCC[-/TCT]TCTTCTTCTTCTTCC	84132
rs750052666	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6111001	ACTATTGTTTTTATA[G/T]TTGAGTGATGTGTTT	84132
rs750115455	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6109611	GTTGGCCAGGCTGGT[C/G]TCGAACTCCTGGACT	84132
rs750140725	snp	C/T	3.76279e-05	0.00433734	intron-variant	USP42	GRCh38.p7	7:6140039	TGAATTCTTGATCTT[C/T]TGTGAGCTCCCATGT	84132
rs750145558	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077863	AGCTAATTTTTTTGT[A/G]CTTTTAGTAGAGACA	84132
rs750162043	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6137375	CATTCATCCATTCAT[A/T]TGAGATGGAGTCTCG	84132
rs750169664	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6088071	TTGGGAGGCCAAGGC[A/G]GGAGGATTGCTTGAG	84132
rs750183072	snp	C/T	3.6547e-05	0.0042746	missense	USP42	GRCh38.p7	7:6154138	CCGGCTCCGCCTGCG[C/T]GGTCGGAGGAGCCCT	84132
rs750188175	snp	C/T			intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116924	AAATTCAGAAGCTCC[C/T]GATGTCCAGAATTAG	84132
rs750231643	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114784	CAAGCTCTGCCTCCC[A/G]GGTTCACGCCATTCT	84132
rs750242421	snp	C/G	1.65611e-05	0.00287755	missense	USP42	GRCh38.p7	7:6140146	AGACAGACACACCCA[C/G]GCCACCACTCTTGTT	84132
rs750306082	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6090089	CAGATCACCTGAGAT[C/T]GGGAGTTCGAGACCA	84132
rs750318624	snp	A/C	1.83135e-05	0.00302596	synonymous-codon	USP42	GRCh38.p7	7:6157028	GAAAGCAGGGATGAC[A/C]GGTGTCGTCTCTTTG	84132
rs750335722	snp	A/G	3.72329e-05	0.00431452	missense	USP42	GRCh38.p7	7:6150021	CTGGTGCCCTATGGC[A/G]CCGAGTCCTCTGAGG	84132
rs750349066	snp	A/G	4.11887e-05	0.00453791	missense	USP42	GRCh38.p7	7:6146155	ATTTATAGGCTAGCA[A/G]TGGCCTCTGGTATCA	84132
rs750366607	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6160219	AGTCTGTGGATTAAT[G/T]GGCCGTTAATTAACA	84132
rs750388763	snp	C/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161822	GTGAACACAGTATCT[C/G]CAAGAGCTCTGACAG	84132
rs750390383	snp	A/T	1.7978e-05	0.00299811	intron-variant	USP42	GRCh38.p7	7:6147696	GAATCTCTCCTAAGG[A/T]GGTGTCCTGTGTCAC	84132
rs750394783	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138472	AAACTTGAGACAAAA[C/T]AGCCAGTTTATTCAA	84132
rs750406234	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126891	GATAAATGCCCAGGA[C/T]TGCAAATGCTGGGTT	84132
rs750454301	snp	C/T	1.65974e-05	0.0028807	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115317	CTTTCTTGTTTATTT[C/T]TCTAGCCCTAGGTGA	84132
rs750455112	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6131331	AATACAAACATTAGC[C/T]GGGTATGGTGGTGCA	84132
rs750457038	snp	A/G	1.67413e-05	0.00289316	intron-variant	USP42	GRCh38.p7	7:6142915	TGATGTGGTGTTTGT[A/G]CCTCTTCTCTTCCCA	84132
rs750474626	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6155603	TGTTATATTTTCCTG[A/C]AATTCAGTGGCTGTG	84132
rs750508906	snp	C/T	1.65614e-05	0.00287757	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115420	AGTTGGAGCTGGGCT[C/T]CAGAATTTGGGCAAT	84132
rs750516544	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6099057	AAAATTCAACCTTTT[C/T]TAATGTTCTGCTCCT	84132
rs750522759	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6151877	CGTTGCCCTTGGACT[G/T]TTACAGTGACGGGAG	84132
rs750545167	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6083661	TAAGTATATAGTATA[C/T]TGAGATATGTATATA	84132
rs750588042	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6156111	ATCCATGATGAGATG[C/G]ATGAGCAGGAGCAGA	84132
rs750635079	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6132077	AGCTGGGACTACAGG[C/T]GTTCACCACCATGCC	84132
rs750643430	snp	A/G	2.80919e-05	0.00374768	missense	USP42	GRCh38.p7	7:6154243	GCACCCGAGGCCGCA[A/G]AGCGGCCGCCAGCTC	84132
rs750654234	snp	A/G	1.71138e-05	0.00292516	intron-variant	USP42	GRCh38.p7	7:6141000	GTAAATTTCATAATT[A/G]TGGGAGTAATTACAT	84132
rs750658200	snp	C/T			intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153333	AGGAATTGGAAGAAC[C/T]AGAGGGATATCCAGA	84132
rs750683450	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131604	TCATCCTTTGGCTGG[A/G]GAGAGTGGGAGCGGG	84132
rs750717294	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081197	GTGGGAGTGTCTTCC[C/T]CCGACACCCCGTATA	84132
rs750728748	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6160525	GCCGCCTGCCTCCAA[C/G]TCACTAACCCTGCGC	84132
rs750745458	in-del	-/AATG			intron-variant	USP42	GRCh38.p7	7:6117792	AATTTGTACTTTCAT[-/AATG]AATAATGCTGAACCT	84132
rs750746502	snp	A/C/G			intron-variant	USP42	GRCh38.p7	7:6125726	CTTTTTATGTATTCA[A/C/G]ATTTCCATTTGGTAT	84132
rs750773438	snp	A/G	3.35137e-05	0.00409338	synonymous-codon	USP42	GRCh38.p7	7:6150203	CAGCGACAGTGACCC[A/G]AAAGAAAACGGCCTA	84132
rs750796786	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6117392	CACTTGATCGTATTG[C/T]TGAGTAGGATTCCAT	84132
rs750800362	in-del	-/TTGT			intron-variant	USP42	GRCh38.p7	7:6125785	TTTGATGCTCAGGGG[-/TTGT]TTATTTTACTTTGTT	84132
rs750822935	snp	A/C/G	0.000122227	0.00781656	stop-gained, missense	USP42	GRCh38.p7	7:6154775	ACGCTGCCCGGGACT[A/C/G]GAAGCCCTTCCACGG	84132
rs750865219	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6140488	GCCTTCGACAGTTGG[A/C]GTAGTGTTCCATTTA	84132
rs750888460	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096999	CATGATCTTGGCTCC[C/T]GGGTTCAAGTGATTC	84132
rs750950311	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6120329	CTCACTGTAACCTCC[A/T]CCTCTTCGGTTTAAG	84132
rs750959096	snp	C/T	0.000134482	0.00819896	missense	USP42	GRCh38.p7	7:6153961	CCCGAGGAGCCTCCG[C/T]CCAGCGCCGGCGAGG	84132
rs750960301	snp	A/T	3.31513e-05	0.00407118	intron-variant	USP42	GRCh38.p7	7:6159435	AAAATCTCTTTCCTG[A/T]CCTTTGCTTTCTAGG	84132
rs750977105	snp	C/T	3.57577e-05	0.00422819	missense	USP42	GRCh38.p7	7:6153995	TCGTGGGGGACACAG[C/T]ACCCCCTGACCTGTG	84132
rs751009297	snp	A/G	5.53388e-05	0.00525988	intron-variant	USP42	GRCh38.p7	7:6135817	GTATTTTGCTAATTT[A/G]GAGGATTATCATCTA	84132
rs751013700	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6145250	GCAGGACAATCACTT[A/G]AACCCGGGAGGCGGA	84132
rs751014430	snp	A/T	1.89708e-05	0.00307978	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111187	ATCAGCCTATCAGAA[A/T]CAGCCTGGCAGCTCC	84132
rs751018486	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6111104	CTGATGAAACAAATA[C/T]ATACTTTTCATCTTT	84132
rs751030251	snp	A/T	1.72092e-05	0.00293331	intron-variant	USP42	GRCh38.p7	7:6149575	AGGTGCGCTCTGCTT[A/T]CTTCCAGAATCCACC	84132
rs751052141	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6145201	AGCTGGGCGTGGTGG[C/T]GCACCTGTAATCCCG	84132
rs751104746	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6082905	TGTGAGCCACTGCGC[C/T]TGTGTCTCTATTAAA	84132
rs751107742	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120592	GGCATGAGCCACTAT[A/G]CCTGGCCTAGGCCAT	84132
rs751109495	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104648	GAAGCACAGGGCGGA[A/C]GGAGCCCTTTCGCCG	84132
rs751185779	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6101003	AGGATATCTAGAAGT[C/G]AGGCTTGAGACAGAA	84132
rs751224591	snp	A/G	1.78557e-05	0.0029879	synonymous-codon	USP42	GRCh38.p7	7:6154104	CTCGGCGTTGGCGGA[A/G]GCCCCGGAAGGGTTG	84132
rs751276625	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6150569	TCCAGTAGCCTCCAG[A/C]TGTGTCAGTATTTGA	84132
rs751284997	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6157820	CAGAGCGCTGGCTGC[C/T]CCTGCCAGGTGTCCT	84132
rs751291084	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6134417	ATGTTATTGGGTGCT[A/G]GGATTTTTGTATTTC	84132
rs751292352	snp	A/T	1.97295e-05	0.00314076	intron-variant	USP42	GRCh38.p7	7:6111087	GAGATTGCTTTTCTC[A/T]CCTGATGAAACAAAT	84132
rs751318258	in-del	-/TTCTC			intron-variant	USP42	GRCh38.p7	7:6091211	TTACACACTTTTCTT[-/TTCTC]TTCTCTTCTCTTCTC	84132
rs751326069	snp	C/T	2.0271e-05	0.00318357	intron-variant	USP42	GRCh38.p7	7:6140024	CATGGCTGTCCTGTT[C/T]GAATTCTTGATCTTT	84132
rs751330197	snp	A/G	4.8432e-05	0.00492074	intron-variant	USP42	GRCh38.p7	7:6146140	CTTTTATTGGCTCTC[A/G]TTTATAGGCTAGCAA	84132
rs751362278	snp	G/T	1.76842e-05	0.00297352	missense	USP42	GRCh38.p7	7:6154064	CCCAGGACGCAAAGG[G/T]GATGATCGCGGAGGG	84132
rs751372333	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138615	CCCTGGGCCGTAGAC[C/T]GGTACCCAATGTGGC	84132
rs751390750	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6094605	AGTTCATTGTCACCT[A/G]TGATGGTTCATCCAG	84132
rs751393269	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6092704	TAAATTAATATTTTG[A/T]CAATCCATAAAGGAG	84132
rs751415609	snp	C/T	2.62216e-05	0.00362079	synonymous-codon	USP42	GRCh38.p7	7:6139114	TAGGCACTTCCGTTT[C/T]GGAAACCAAGAAGAT	84132
rs751417357	snp	C/G	0.000120402	0.007758	missense	USP42	GRCh38.p7	7:6153878	GCAGCACCAAGAAGG[C/G]TCCGCCGCCCCGCGA	84132
rs751419797	snp	A/T	6.1476e-05	0.00554385	intron-variant	USP42	GRCh38.p7	7:6146298	GTATGTCATTTCTTC[A/T]TGTCTTATCAACATG	84132
rs751442400	in-del	-/TG			intron-variant	USP42	GRCh38.p7	7:6138064	AATGTCATTGCTCTG[-/TG]TGTGTGTGTGTATCC	84132
rs751446288	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6090711	CAGAGTGAGACTCTG[C/T]CTCAAATAAACAAAA	84132
rs751479415	snp	G/T	1.70688e-05	0.00292132	missense	USP42	GRCh38.p7	7:6156842	AAAAAGAAGAGACAT[G/T]CAAGAAAATCAGAGG	84132
rs751479428	in-del	-/TG	1.72859e-05	0.00293984	intron-variant	USP42	GRCh38.p7	7:6115539	GTAAGTGTTCCGTGT[-/TG]TGTTTGTAGTATTGT	84132
rs751480444	snp	C/T	1.65677e-05	0.00287812	missense	USP42	GRCh38.p7	7:6149896	CAGTACAGTCTACCT[C/T]GAACGCATCTACGAT	84132
rs751480553	snp	C/T	1.73249e-05	0.00294315	missense	USP42	GRCh38.p7	7:6154588	AGCCCTGGCGAGCGC[C/T]GCTCTCTGGGCAGGT	84132
rs751598676	snp	A/T	1.66007e-05	0.00288098	intron-variant	USP42	GRCh38.p7	7:6140226	TAAGTTGATAAAATG[A/T]TACACACATGTGGTT	84132
rs751619468	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6083823	CCTTACTCAATCTGC[A/G]TATTCAGAGCTGTTC	84132
rs751652050	snp	A/C	1.69761e-05	0.00291337	intron-variant	USP42	GRCh38.p7	7:6140989	TGGAGATAAAGGTAA[A/C]TTTCATAATTATGGG	84132
rs751654348	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6122863	TCTTGAACTGCTGGC[A/G]CCCAGGCTAGAGTGC	84132
rs751673278	snp	C/T	3.6205e-05	0.00425455	synonymous-codon	USP42	GRCh38.p7	7:6154710	GAAGTTCTACCCCGA[C/T]AGGCCGCGCTGGGAC	84132
rs751690088	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6156304	AGTAACTACTGGTTT[C/T]GGGAAAAGTTAGCAG	84132
rs751696021	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6148358	AACCCCCCAAAAAAA[C/T]AAAAACCCCAAAATA	84132
rs751701988	snp	A/G	3.71478e-05	0.00430958	missense	USP42	GRCh38.p7	7:6150120	CCCGGCCAAGATGCC[A/G]AAGATGAGGAGGCCA	84132
rs751711716	snp	A/C/T	0.000112094	0.0074857	synonymous-codon, missense	USP42	GRCh38.p7	7:6154195	AGCGGGGACCACGCC[A/C/T]GGGACGCTCAGGACC	84132
rs751787723	snp	A/G	6.84592e-05	0.0058502	missense	USP42	GRCh38.p7	7:6147761	GATGTGAAAAATGGA[A/G]GTGAACTTACTCATC	84132
rs751790404	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6115923	GGACAACATAGTAAG[A/T]CCCCATCTCTACTAA	84132
rs751809383	snp	C/T	0.000115667	0.00760396	missense	USP42	GRCh38.p7	7:6154768	GCCCTGTACGCTGCC[C/T]GGGACTGGAAGCCCT	84132
rs751843402	snp	A/C/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114901	TTCACCTTGTTAGCC[A/C/G]GGATGGTCTCGATCT	84132
rs751848293	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6084978	CACACCTCGGCCTCT[C/T]AGAGTGCTGCGATTA	84132
rs751860307	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6141703	AGCTGGGACTACAGC[A/G]ACTGTGCCCAGCCTG	84132
rs751876157	snp	A/G	2.9609e-05	0.00384755	intron-variant	USP42	GRCh38.p7	7:6135804	TGTGTATATGGTTGT[A/G]TTTTGCTAATTTGGA	84132
rs751878108	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6105894	CCGTGGGGTCACTTG[-/T]TTATGGGAAAACATG	84132
rs751926721	snp	C/G	1.9742e-05	0.00314175	missense	USP42	GRCh38.p7	7:6153956	TCGCCCCCGAGGAGC[C/G]TCCGCCCAGCGCCGG	84132
rs751938391	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6107920	ATCTTTTCTATTTCT[A/G]CTTGAGTTCAGAAAC	84132
rs751941690	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6102010	CCTGGGAGGTGGAGG[C/T]TGCAGTGAGCCGAGA	84132
rs751985335	snp	A/G	3.96416e-05	0.00445188	missense	USP42	GRCh38.p7	7:6157047	GTCGTCTCTTTGAGT[A/G]TGGCCAGGGTAAGAG	84132
rs751993935	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6118187	TCACTTGAGCCCAGG[A/G]TTTCAAGACTAGCCT	84132
rs752003284	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6100812	GCTGGGATTATAGGC[A/G]CGCGCTACCACACTC	84132
rs752010753	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6108663	TTTTTGTATTTTCAG[A/T]AGAGACAGGGTTTCA	84132
rs752024410	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096543	TCAGGTTCATCTGTA[C/T]GTTGTTGGGGTCTGT	84132
rs752035446	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131439	TGATCCCGCCACTGC[A/G]CTCCAGCCTGGGTGA	84132
rs752036894	snp	C/T	1.65605e-05	0.0028775	missense	USP42	GRCh38.p7	7:6149713	CTGTCCAAAACTGGT[C/T]AGTTAATAGGTCCTC	84132
rs752050893	in-del	-/TCTT			intron-variant	USP42	GRCh38.p7	7:6117017	CTCTCTTTCTCTCTC[-/TCTT]TTCCCAGCTTTACTG	84132
rs752088016	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6142733	CTACAAAAAAATGAA[A/G]AATTTAGCTGGGCAT	84132
rs752089209	snp	A/G	1.84123e-05	0.00303411	synonymous-codon	USP42	GRCh38.p7	7:6155127	TCTAGAAGAGCCTAA[A/G]GCAAAGAAGCACAAA	84132
rs752099114	snp	A/G	0.00015365	0.00876364	missense	USP42	GRCh38.p7	7:6139101	TTACAGGTATAGCTA[A/G]GCACTTCCGTTTTGG	84132
rs752100850	snp	C/T	8.58819e-05	0.00655237	synonymous-codon	USP42	GRCh38.p7	7:6150287	CTTTGCTAAGGCAAA[C/T]GGTCTTCCTGGAAAG	84132
rs752101867	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6124840	TTTTTTCATGGTGGT[-/A]TACTTTAGGTTATAT	84132
rs752105248	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6158640	GATGAGGACAGGCAC[C/T]AGCACTGCCGGTGAG	84132
rs752120985	snp	A/G	9.54973e-05	0.00690938	missense	USP42	GRCh38.p7	7:6153917	CCCCCGCTACCAAAG[A/G]AGGCGCCTGGGAGGC	84132
rs752121538	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6101063	GGCCTTGAGGGGAGC[A/G]CTCTAGGGAGGAAGG	84132
rs752157155	snp	A/C/T	3.57508e-05	0.00422781	missense	USP42	GRCh38.p7	7:6154100	GGGACTCGGCGTTGG[A/C/T]GGAAGCCCCGGAAGG	84132
rs752177633	snp	A/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113565	AACCACTAATAAGTC[A/T]CTTCAGATGGAGAAT	84132
rs752193927	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6085404	TCCTGGGATTTTAGG[C/T]GTGGGCCACCGTGCC	84132
rs752215986	in-del	-/A			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104469	AGGGCGAAGCCCACG[-/A]AGCGGAGGATTTCTC	84132
rs752282108	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6087568	TCTTGAACTCCTGGA[C/G]TGAAGCAATCCACCC	84132
rs752309100	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6134641	TCCCTGGCTTCTCCC[C/G]ACTAGATGCTGCAGC	84132
rs752331174	snp	C/T	0.000260858	0.0114176	synonymous-codon	USP42	GRCh38.p7	7:6154581	CAGGCTCAGCCCTGG[C/T]GAGCGCCGCTCTCTG	84132
rs752347831	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6142509	GCGTGAGCCACCACG[C/T]CCGCCCGGAAAATTT	84132
rs752369543	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6159151	TTCTCTTTCAAACTC[C/G]TCCTCTGGCTCTGTT	84132
rs752376736	snp	C/T	1.68883e-05	0.00290584	synonymous-codon	USP42	GRCh38.p7	7:6145623	CCACACTGGTTTTAA[C/T]TGCCATGCTGGCCAT	84132
rs752408701	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6102008	AACCTGGGAGGTGGA[C/G]GTTGCAGTGAGCCGA	84132
rs752417145	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6125795	AGGGGTTGTTTATTT[C/T]ACTTTGTTGTTGATT	84132
rs752434566	snp	A/T	3.02549e-05	0.00388928	intron-variant	USP42	GRCh38.p7	7:6135967	GTAAGTATTAACTAT[A/T]GTAGTTTTATATTTG	84132
rs752469806	snp	C/G	1.65608e-05	0.00287752	missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115404	GGCAACAAACTCATA[C/G]AGTTGGAGCTGGGCT	84132
rs752480491	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6120623	CTTTAGTTTCTCGTT[C/G]CCCAGGCTGGAGTGC	84132
rs752490177	snp	C/T			missense	USP42	GRCh38.p7	7:6154174	CAGCCACTCCTTGTT[C/T]ACCCCAGCGGGGACC	84132
rs752501237	snp	A/G	1.65658e-05	0.00287795	missense	USP42	GRCh38.p7	7:6149883	ATTACCAATTCTGCA[A/G]TACAGTCTACCTCGA	84132
rs752532722	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130174	TTTGGTGTTATCTTA[C/T]AAGACACTGAGTCTT	84132
rs752550552	snp	C/T			synonymous-codon	USP42	GRCh38.p7	7:6155178	ATCCAAAGACAAACA[C/T]CGAGACCGCGACTCC	84132
rs752586698	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6112607	ATTTGAGGACATGAA[G/T]ATTTGAAATACAATA	84132
rs752587116	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6140270	AGTAGGACAGGGTTA[C/G]TCCTACTAGGAAGGA	84132
rs752588819	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6107290	AGTGATTGTTCTGAA[A/G]GTATGTTTATCCCCT	84132
rs752593817	snp	G/T	4.18533e-05	0.00457437	missense	USP42	GRCh38.p7	7:6153823	CCTGGCAGCCCCGCC[G/T]CCGAATCCCTGGAGG	84132
rs752597679	snp	C/G	3.01891e-05	0.00388506	intron-variant	USP42	GRCh38.p7	7:6156730	GTGTTTTAGGGTTTT[C/G]AATTCTGGCTTTTCC	84132
rs752613781	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080923	AGTGTAATGTTTACA[C/G]CGAATTCTGCCACTG	84132
rs752653345	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6145263	TTGAACCCGGGAGGC[A/G]GAGCTTCCAGTGAGC	84132
rs752674627	in-del	-/TTC			intron-variant	USP42	GRCh38.p7	7:6092055	TCTTCTTCTTCTTCT[-/TTC]TTCTTCTTCTTCTTC	84132
rs752690115	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6121323	TGTTTGATGCTTGAA[C/T]GTTAAACCAACCTTG	84132
rs752694162	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6151152	TGCACAGGGCACTTA[A/C]CATGAATGGAGCTGG	84132
rs752695512	snp	A/G	1.65627e-05	0.00287769	missense	USP42	GRCh38.p7	7:6149823	CAACCTAACCTTCAT[A/G]GTAATTCTTTGGAGA	84132
rs752699163	snp	C/T	4.99006e-05	0.00499478	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115296	TGCAAAGCTTGGTTT[C/T]TGACTCTTTCTTGTT	84132
rs752735890	snp	A/G	1.79461e-05	0.00299545	intron-variant	USP42	GRCh38.p7	7:6147705	CTAAGGAGGTGTCCT[A/G]TGTCACCCTAAGTAT	84132
rs752736131	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6095451	GAGGCAGGCAGATCA[C/T]GAAGTCAGGAGTTTG	84132
rs752737907	snp	C/T	1.65364e-05	0.0028754	missense	USP42	GRCh38.p7	7:6150118	CTCCCGGCCAAGATG[C/T]CGAAGATGAGGAGGC	84132
rs752738306	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6079359	GCTACGCTGGAGGCT[A/G]AGGCAGGAGAATCGC	84132
rs752804310	snp	C/T	1.70365e-05	0.00291855	missense	USP42	GRCh38.p7	7:6156960	CTCTCTCTGGTGGCC[C/T]GCCTCTGGAAGGCGT	84132
rs752808563	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6106508	TAAGACTAGTATTTA[A/C]AGCAAAGGAAACACT	84132
rs752842085	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6137205	ACTGTAATCTTTTTG[C/T]CTAGAAAGCCACTGA	84132
rs752859603	snp	A/T	7.05741e-05	0.00593987	synonymous-codon	USP42	GRCh38.p7	7:6153909	TCCCGGCACCCCCGC[A/T]ACCAAAGAAGGCGCC	84132
rs752901112	snp	C/T			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161734	TTGGAGGGGTGTTTG[C/T]TGGACCCAACAATAT	84132
rs752930454	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6093714	CCTCCCTTCTTTACT[G/T]TTTTGTGGTAAAATA	84132
rs752933903	snp	A/G	1.93932e-05	0.00311387	missense	USP42	GRCh38.p7	7:6150045	TCTGAGGACTCTGAC[A/G]AGGAGTCAAAGGGGC	84132
rs752937038	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6144199	AAAAATTGCTAAGGT[A/G]TGTGGATGATGTCAT	84132
rs752963044	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6142221	TTTGTTTCTTTTTTC[-/T]TTTTTTTTTTTTTGA	84132
rs752982324	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6105596	GGCGCCCCCTCCCCA[A/G]GCCTAGCCACCTGGC	84132
rs752996936	snp	A/G	7.52233e-05	0.00613237	missense	USP42	GRCh38.p7	7:6157035	GGGATGACAGGTGTC[A/G]TCTCTTTGAGTATGG	84132
rs753053527	snp	C/T	8.10537e-05	0.00636555	missense	USP42	GRCh38.p7	7:6154337	GGGTCGAGGACGCCG[C/T]GGCGCCGAAAGCCCC	84132
rs753102162	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6109437	AGTCTCTCTATGTCA[A/G]TCTGGAGTGCAGTGG	84132
rs753109615	in-del	-/CCG			cds-indel	USP42	GRCh38.p7	7:6153879	AGCACCAAGAAGGCT[-/CCG]CCGCCGCCCCGCGAT	84132
rs753117122	snp	C/G	0.000101276	0.00711532	intron-variant	USP42	GRCh38.p7	7:6147906	AGGTAACAGTCCTTA[C/G]GGAGAAGAACATTTT	84132
rs753135066	snp	A/T	1.86128e-05	0.00305058	synonymous-codon	USP42	GRCh38.p7	7:6144154	TGTTCTTACACTTTC[A/T]CTGAAACGTTTTGCA	84132
rs753162238	snp	A/G	1.66363e-05	0.00288407	intron-variant	USP42	GRCh38.p7	7:6143019	AAGTGCAGCAAGTAC[A/G]TTGGGTGGTGACTTG	84132
rs753189945	snp	A/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081063	ATGGCAAGCTCTCAG[A/T]GAGTCTTGTACCTAA	84132
rs753196314	snp	C/T	0.000171807	0.00926681	synonymous-codon	USP42	GRCh38.p7	7:6154977	AACTGCACTTGTAGC[C/T]GGAGACAACTGTAAC	84132
rs753205231	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6098986	TCCTTTGTCTCAGGG[G/T]CTCACTCCTTCCTTA	84132
rs753207750	snp	A/C/G	0.000100883	0.00710149	missense	USP42	GRCh38.p7	7:6154945	GCCCCGCACCCCGAC[A/C/G]GCTTCTCCCACGACA	84132
rs753222002	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6122940	GTGATTCTCATACCT[C/T]AGCCTCCTGAGCAGC	84132
rs753224069	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6133282	ATTGTTATTTCTTGA[A/G]ATATTTATGCTGTCC	84132
rs753237713	snp	C/G	3.56411e-05	0.00422129	missense	USP42	GRCh38.p7	7:6154001	GGGACACAGCACCCC[C/G]TGACCTGTGTGATCC	84132
rs753241645	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6151461	TTTTTTTGTTTGAGA[C/T]GGAGTCTCGCTGTGT	84132
rs753278961	snp	A/G	5.09022e-05	0.00504465	synonymous-codon	USP42	GRCh38.p7	7:6154296	CGGTCACCCGGAAGG[A/G]GACGCTGAGCCTAGC	84132
rs753283464	in-del	-/TATT			intron-variant	USP42	GRCh38.p7	7:6089028	TTTCTTTTCTATATT[-/TATT]TATTTATTTATTTAT	84132
rs753295973	snp	A/C	0.000143379	0.00846576	synonymous-codon	USP42	GRCh38.p7	7:6154572	CCACGGCGACAGGCT[A/C]AGCCCTGGCGAGCGC	84132
rs753301767	snp	C/T	3.99433e-05	0.00446879	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6135842	CATCTATCTTTCAGG[C/T]CATGCAGAAGGCTTT	84132
rs753312819	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103170	AGGTGGAGACAGCCA[A/G]TAAATGATTGGATGT	84132
rs753337542	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137252	ATATTGGCCCTTGGC[A/G]TTATTGATAGACCAC	84132
rs753342582	in-del	-/CAAT			utr-variant-3-prime	USP42	GRCh38.p7	7:6161112	TTTGTGGAACTGTTC[-/CAAT]CAATCAATCAATTTC	84132
rs753357609	snp	A/G	2.23551e-05	0.00334321	missense	USP42	GRCh38.p7	7:6135949	TCATCAATGAGATGC[A/G]GCGTAAGTATTAACT	84132
rs753404492	snp	A/G			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161683	GAAGTCGGCACCTTC[A/G]GCCAGGCCATCCCAC	84132
rs753408011	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6159285	ACCCTGGGAGCAGCC[C/G]CTGAGCGCTGGGACA	84132
rs753424898	in-del	-/GAG	5.51101e-05	0.005249	cds-indel	USP42	GRCh38.p7	7:6150126	CAAGATGCCGAAGAT[-/GAG]GAGGCCACTCCGCAC	84132
rs753432698	in-del	-/TTTTTTTTTTTT			intron-variant	USP42	GRCh38.p7	7:6082604	TTTTCTTTCTTTCTG[-/TTTTTTTTTTTT]TTTTTTTTTTTTTGA	84132
rs753459051	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077086	CACCATATTGGTCCG[A/G]CTGGTCTTGAACTCC	84132
rs753476128	snp	A/T	3.15791e-05	0.00397348	intron-variant	USP42	GRCh38.p7	7:6156722	GTGGTTTTGTGTTTT[A/T]GGGTTTTGAATTCTG	84132
rs753494558	snp	C/T	6.40882e-05	0.00566039	missense	USP42	GRCh38.p7	7:6154516	ACCTGCCCCCGGGAG[C/T]GCGACCGCCAGGACC	84132
rs753499898	snp	C/T	1.65627e-05	0.00287769	synonymous-codon	USP42	GRCh38.p7	7:6149816	TCAGTCTCAACCTAA[C/T]CTTCATAGTAATTCT	84132
rs753527593	snp	C/T	2.11401e-05	0.00325109	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111330	TAGTTTATTCGAGTT[C/T]ATCTGTACCTGATAA	84132
rs753533046	in-del	-/TTTCT			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104072	GGGCTACAGACCCTG[-/TTTCT]TTTCTTTTCTTTTCT	84132
rs753552675	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6127583	ATTAAAAAAAATTAT[C/T]TGGGCATATTTGTGT	84132
rs753569905	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6118944	TTGTGGCCAACTGCA[A/G]TGGCTCATGTCTGTA	84132
rs753572980	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6146569	CTCCGAAAGTTGAGG[A/T]GGGAGGATTACCTGA	84132
rs753574568	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6156063	GTATTTTTAAAAAGC[C/T]AAATTGGTTGGTGAT	84132
rs753575326	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6112812	ACAATTTGTCTTCCA[A/G]TGTGGCCCAGGGAAG	84132
rs753588505	snp	C/T	1.65778e-05	0.002879	intron-variant	USP42	GRCh38.p7	7:6145499	GAAATGTTTCTCCTG[C/T]TTCCATTTCCTTCTA	84132
rs753621341	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6149477	AACTTGTTAGTCCTG[-/A]AAAAAAAAAAAAAGC	84132
rs753641042	snp	A/G	1.65792e-05	0.00287912	intron-variant	USP42	GRCh38.p7	7:6150520	AGGTAACGTAAGAGT[A/G]CATCTGAGGCACGTG	84132
rs753671395	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6143324	GTGGCTGGGCACGCA[-/CT]GTCTGCCAAATAGCA	84132
rs753671427	snp	C/T	4.99963e-05	0.00499956	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115276	CTATTTATTTAGCTT[C/T]AGTATGCAAAGCTTG	84132
rs753708877	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6135723	AAGTAGATAGCTCAA[C/G]GCATGCATATAGCAG	84132
rs753736171	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6131022	GCCCTGAGATGATTA[C/G]GGCAGAGGAGTTTTG	84132
rs753757499	snp	G/T	0.000103952	0.00720869	missense	USP42	GRCh38.p7	7:6147749	TCCAGGTCCCATGAT[G/T]TGAAAAATGGAGGTG	84132
rs753797224	snp	A/C	5.311e-05	0.00515288	intron-variant	USP42	GRCh38.p7	7:6140049	ATCTTTTGTGAGCTC[A/C]CATGTGTTTGAAATC	84132
rs753820844	snp	A/G	1.83095e-05	0.00302563	missense	USP42	GRCh38.p7	7:6154144	CCGCCTGCGCGGTCG[A/G]AGGAGCCCTGCGAGC	84132
rs753829899	snp	C/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113631	TGTTTTTGTTTTTGT[C/T]TTTTTTTTGAGACGA	84132
rs753871997	snp	A/G	1.68727e-05	0.00290449	missense	USP42	GRCh38.p7	7:6149959	CCCGCAGTGAATCCT[A/G]CTCCCAGCCCGTGAT	84132
rs753912389	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6140425	GCACTGCTTCCATTT[C/G]TCTCTTCGTATTAGC	84132
rs753945019	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6106850	GGATTACAGGCTTGG[C/T]CCACCATGCCCCACC	84132
rs753965561	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6095774	ACTGGATGGGTATTT[C/T]GATTTTTGTTTTTGA	84132
rs753994029	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6098661	GGTTCAAACGATTCT[-/C]CTGCCTCAGCCTCCT	84132
rs754000991	snp	A/G	4.9081e-05	0.00495359	synonymous-codon	USP42	GRCh38.p7	7:6154290	CCCGGCCGGTCACCC[A/G]GAAGGGGACGCTGAG	84132
rs754015722	snp	C/G	1.68199e-05	0.00289994	synonymous-codon	USP42	GRCh38.p7	7:6156931	CCAGTTCCGGAGAGC[C/G]CAGGGTGGCTTTCCT	84132
rs754028139	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6139706	GTAGATCTCCCTCTG[C/T]ATTCTCCCTGCCCTG	84132
rs754043868	snp	A/G	1.65636e-05	0.00287776	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6115462	CAATGCAGCACTGCA[A/G]TGTTTAACCTACACA	84132
rs754073417	snp	A/C	0.00011564	0.00760308	missense	USP42	GRCh38.p7	7:6153881	GCACCAAGAAGGCTC[A/C]GCCGCCCCGCGATCC	84132
rs754084839	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6134286	TATTGTCTTCTGATT[A/G]TATTTTCTGTGTTAT	84132
rs754093372	snp	A/G	1.74476e-05	0.00295356	intron-variant	USP42	GRCh38.p7	7:6149562	TGGAGCTCTGACCAG[A/G]TGCGCTCTGCTTACT	84132
rs754095366	snp	C/T	1.66468e-05	0.00288498	intron-variant	USP42	GRCh38.p7	7:6142929	TGCCTCTTCTCTTCC[C/T]AGGCTGCTCAGAGTG	84132
rs754102744	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6094918	TCAGCCTCCTGAGTA[A/G]CTGGGATTACAGGTG	84132
rs754105113	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6157946	TGGTGTCCGGTGACC[G/T]CTCACCCTCGAGAGG	84132
rs754175187	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6097386	GGTCCCTGTGGGTCC[-/T]TTTTTTTTTTTTTTT	84132
rs754215556	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6145054	TGAAAGGTGGCTAGG[A/C]CAGGTGCAGTGGCTC	84132
rs754218270	snp	C/T	8.38455e-05	0.00647423	intron-variant	USP42	GRCh38.p7	7:6147897	ACATGATAAAGGTAA[C/T]AGTCCTTAGGGAGAA	84132
rs754224195	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6099095	TAAGTCCTCTGCCTG[G/T]TTTTCAGGACTGTCT	84132
rs754247311	snp	C/T	5.92575e-05	0.00544291	missense	USP42	GRCh38.p7	7:6154250	AGGCCGCAGAGCGGC[C/T]GCCAGCTCCTGTGCT	84132
rs754259896	snp	C/T			utr-variant-3-prime	USP42	GRCh38.p7	7:6161231	TGATACAGCGTCTCT[C/T]GTCTTCACTGATACT	84132
rs754266876	snp	A/G	3.34919e-05	0.00409204	missense	USP42	GRCh38.p7	7:6150213	GACCCGAAAGAAAAC[A/G]GCCTAGCGCCTGATG	84132
rs754270575	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6149505	AGCAAAATGGGAAGG[A/G]CCCATCAGCCAAAAT	84132
rs754298296	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6117952	TGTTGAGCTTAGAGA[A/G]TTCTTTATATATCCT	84132
rs754303445	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6158670	GGACGGGTTGCCTGC[A/G]GGCCTTGTAGACGTT	84132
rs754304038	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081225	ATACCTCCGCTTTAA[C/G]ATGAGAGAATCTTCT	84132
rs754337929	snp	C/T	1.76658e-05	0.00297197	missense	USP42	GRCh38.p7	7:6154042	ACAGGCGATGCGAGC[C/T]CGTTGTCCCAGGACG	84132
rs754376621	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137524	CCACCACACCTGGCT[A/G]ATTTTGTAGTTTTAG	84132
rs754387169	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081412	CCCCGGCCCCGCCGC[C/T]TTCCACTTTGCGCTC	84132
rs754423788	snp	A/G	1.7074e-05	0.00292177	missense	USP42	GRCh38.p7	7:6150279	GAAAATCCCTTTGCT[A/G]AGGCAAACGGTCTTC	84132
rs754427122	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6106949	ATATTTGTAACAGTA[A/G]TATTTAGAAGCTTTA	84132
rs754446171	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6099456	CCTGACCTCATGATC[C/T]GCCCGCCTCGGCCTC	84132
rs754488840	snp	C/G	1.77401e-05	0.00297821	missense	USP42	GRCh38.p7	7:6154015	CCTGACCTGTGTGAT[C/G]CCGGGAGCTTAACAG	84132
rs754526590	snp	A/G	3.31477e-05	0.00407096	utr-variant-3-prime, intron-variant	USP42	GRCh38.p7	7:6159464	GGTGATTGAAAACTC[A/G]GCCTCAAAACAAAAA	84132
rs754532431	snp	A/T	1.65754e-05	0.00287879	intron-variant	USP42	GRCh38.p7	7:6145501	AATGTTTCTCCTGTT[A/T]CCATTTCCTTCTAGG	84132
rs754564754	snp	A/G	0.000132479	0.00813768	missense	USP42	GRCh38.p7	7:6149668	GGAATTCCAGTGTCA[A/G]CAGGGCTAGTCCTGT	84132
rs754572436	snp	C/T	2.70746e-05	0.00367921	intron-variant	USP42	GRCh38.p7	7:6135963	CGGCGTAAGTATTAA[C/T]TATTGTAGTTTTATA	84132
rs754582251	snp	A/G	1.67494e-05	0.00289386	missense	USP42	GRCh38.p7	7:6150214	ACCCGAAAGAAAACG[A/G]CCTAGCGCCTGATGG	84132
rs754582343	snp	A/G	5.81807e-05	0.00539323	intron-variant	USP42	GRCh38.p7	7:6111105	TGATGAAACAAATAC[A/G]TACTTTTCATCTTTT	84132
rs754585183	snp	C/T	0.000179646	0.0094758	synonymous-codon	USP42	GRCh38.p7	7:6154518	CTGCCCCCGGGAGCG[C/T]GACCGCCAGGACCGC	84132
rs754612179	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6101025	GAGACAGAATTTAGG[C/T]GCACAAGATTTAGGT	84132
rs754627839	snp	C/T	3.88916e-05	0.00440957	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6135845	CTATCTTTCAGGTCA[C/T]GCAGAAGGCTTTTGT	84132
rs754656813	in-del	-/C	1.65912e-05	0.00288016	intron-variant	USP42	GRCh38.p7	7:6150531	AGTACATCTGAGGCA[-/C]CGTGTGGCAGCATAG	84132
rs754691380	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6158077	CTTTGTATGAACTTG[G/T]AGTTAAGAATGGTTT	84132
rs754714649	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6138007	TTTATACATATTTAT[A/G]TAGCAGACATGACTA	84132
rs754726289	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120008	TCTCGCTCTGCCGCC[C/T]GGGCTGGAGTGCAGT	84132
rs754765071	snp	A/G	0.00010596	0.00727797	synonymous-codon	USP42	GRCh38.p7	7:6155175	GAAATCCAAAGACAA[A/G]CACCGAGACCGCGAC	84132
rs754766036	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6093683	TTTTTTCTCTTCCTC[G/T]CCCTCTTTCTCTCCC	84132
rs754782928	snp	C/T	1.65616e-05	0.00287759	synonymous-codon	USP42	GRCh38.p7	7:6149744	AGTGATCCCAGAACA[C/T]CCTAAGAAACAAAAA	84132
rs754783264	snp	C/G	6.30001e-05	0.00561214	intron-variant	USP42	GRCh38.p7	7:6156723	TGGTTTTGTGTTTTA[C/G]GGTTTTGAATTCTGG	84132
rs754800264	snp	A/C	3.31263e-05	0.00406965	missense	USP42	GRCh38.p7	7:6149820	TCTCAACCTAACCTT[A/C]ATAGTAATTCTTTGG	84132
rs754800508	snp	C/T	0.000116085	0.00761769	intron-variant	USP42	GRCh38.p7	7:6150524	AACGTAAGAGTACAT[C/T]TGAGGCACGTGTGGC	84132
rs754815958	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6151949	GTCTGTTGTTGACCG[-/T]TATGTATGAGGTACA	84132
rs754845275	snp	A/G	4.1431e-05	0.00455124	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111232	TGGAGACATGGATGC[A/G]GGTTCTGCCAGCTGG	84132
rs754885701	snp	A/G	1.65932e-05	0.00288034	intron-variant	USP42	GRCh38.p7	7:6140218	TTTGCTTATAAGTTG[A/G]TAAAATGATACACAC	84132
rs754890544	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104787	GACCCCTCCCACACT[A/C]GCCGTGCTTGTTAGC	84132
rs754904453	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077965	GTGGGCGTGAGCCAC[C/T]GGGCCTGGCCCTTAA	84132
rs754925996	snp	C/T			intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153165	GTAATCCCAGCTACC[C/T]GGGAAGCTGGGTCAG	84132
rs754928324	snp	C/T	1.65679e-05	0.00287814	missense	USP42	GRCh38.p7	7:6150482	GGCTTAGCAACAAAC[C/T]GAAAGGCTCGACGGA	84132
rs754974003	snp	C/G	0.000144046	0.00848542	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111353	CCTGATAAATCAAAA[C/G]CATCACCACAAAAGG	84132
rs755018793	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6113086	ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC	84132
rs755040467	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6147947	TTTAAAATGTAACTT[C/G]AAACTCTCAAGTTGA	84132
rs755048591	snp	C/T	0.000156635	0.00884834	missense	USP42	GRCh38.p7	7:6146160	TAGGCTAGCAATGGC[C/T]TCTGGTATCAAATGA	84132
rs755093081	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6084046	TTTTGTTTTGTTTTG[A/G]GACAGAGTCTCGCTC	84132
rs755125474	snp	G/T	1.75594e-05	0.00296301	synonymous-codon	USP42	GRCh38.p7	7:6153882	CACCAAGAAGGCTCC[G/T]CCGCCCCGCGATCCC	84132
rs755178406	snp	C/T			utr-variant-3-prime	USP42	GRCh38.p7	7:6160847	CAGGTCGATTACTTG[C/T]ATTTCATGTAATGTT	84132
rs755183520	snp	C/G/T	6.95258e-05	0.00589565	intron-variant	USP42	GRCh38.p7	7:6116761	TTATGCCAGAATTAA[C/G/T]GTTCTGTTTGCCCTC	84132
rs755192880	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6115930	ATAGTAAGACCCCAT[A/C]TCTACTAAAAATAAA	84132
rs755200881	snp	C/G	3.31334e-05	0.00407009	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6115471	ACTGCAGTGTTTAAC[C/G]TACACACCACCTCTT	84132
rs755211684	snp	C/T	1.69375e-05	0.00291006	missense	USP42	GRCh38.p7	7:6149961	CGCAGTGAATCCTGC[C/T]CCCAGCCCGTGATGA	84132
rs755216479	in-del	-/AAAT			intron-variant	USP42	GRCh38.p7	7:6090715	GTGAGACTCTGTCTC[-/AAAT]AAACAAAAAAACAAA	84132
rs755234383	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6095990	TGGTCTCGAATTCCT[A/C]GACTCAAATCATCCA	84132
rs755248810	snp	C/T			downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161323	ATTTTATTTTTAATA[C/T]GGATATGCTATCAAA	84132
rs755265130	snp	A/C/G	9.23299e-05	0.00679396	missense	USP42	GRCh38.p7	7:6154255	GCAGAGCGGCCGCCA[A/C/G]CTCCTGTGCTGGACA	84132
rs755278718	snp	A/G	3.36061e-05	0.00409901	missense	USP42	GRCh38.p7	7:6156857	TCAAGAAAATCAGAG[A/G]ACTTTGTTAAAGATT	84132
rs755279154	in-del	-/ACG	0.000107881	0.00734362	intron-variant	USP42	GRCh38.p7	7:6139057	GGCTTATTACGTGTA[-/ACG]ATGATAAAGCCTTGT	84132
rs755308989	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6108704	CAGGATGGTCTCAAT[A/C]TCCTGACCTCGTGAT	84132
rs755340026	snp	C/T	1.70883e-05	0.00292299	synonymous-codon	USP42	GRCh38.p7	7:6154971	CGACAGAACTGCACT[C/T]GTAGCCGGAGACAAC	84132
rs755375527	snp	C/G	3.41723e-05	0.0041334	missense	USP42	GRCh38.p7	7:6150281	AAATCCCTTTGCTAA[C/G]GCAAACGGTCTTCCT	84132
rs755392092	snp	G/T	0.000132935	0.00815166	missense	USP42	GRCh38.p7	7:6154915	AGCCCCCGCGCAGGC[G/T]CGCCCCACGCCCTCG	84132
rs755393243	snp	C/G	1.95743e-05	0.00312838	missense	USP42	GRCh38.p7	7:6153841	GAATCCCTGGAGGAG[C/G]CAGATGCGGCCGCCG	84132
rs755427729	snp	A/G	4.90328e-05	0.00495116	missense	USP42	GRCh38.p7	7:6154292	CGGCCGGTCACCCGG[A/G]AGGGGACGCTGAGCC	84132
rs755437513	snp	A/C	3.32105e-05	0.00407482	missense	USP42	GRCh38.p7	7:6142939	CTTCCCAGGCTGCTC[A/C]GAGTGTCAACAAGGC	84132
rs755455967	snp	A/C/G			intron-variant	USP42	GRCh38.p7	7:6118856	CTATTTCTGGACTCT[A/C/G]TTATGTTGTACTGAT	84132
rs755482225	snp	C/T	1.65693e-05	0.00287826	missense	USP42	GRCh38.p7	7:6147834	GTCAGCGGGTTGTCA[C/T]CAACAAACAGGCTGC	84132
rs755482331	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6156385	AGCAGAGATGGGACT[A/G]TTCAGGATGGAGCTA	84132
rs755495274	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6122464	TGTTTTGTTTTGTTT[G/T]TTTGTTTGTTTGTTT	84132
rs755515756	snp	C/T	0.00032408	0.0127254	intron-variant	USP42	GRCh38.p7	7:6142890	CCCAAACACAAGTGA[C/T]GGTGTGCGGTGATGT	84132
rs755535191	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6096544	CAGGTTCATCTGTAC[A/G]TTGTTGGGGTCTGTC	84132
rs755550405	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6102022	AGGTTGCAGTGAGCC[A/G]AGACTGTTCTAGGAG	84132
rs755567239	snp	A/C	1.6832e-05	0.00290099	intron-variant	USP42	GRCh38.p7	7:6147902	ATAAAGGTAACAGTC[A/C]TTAGGGAGAAGAACA	84132
rs755595633	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6087960	ATCTAAATCATTTAG[G/T]AGAGGGACCTGGGAC	84132
rs755616172	snp	C/G	0.000183201	0.00956905	missense	USP42	GRCh38.p7	7:6154419	AGGCCACTACCGCAG[C/G]CGGAGAGAGCGCTCG	84132
rs755616366	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6158649	AGGCACCAGCACTGC[C/T]GGTGAGGACGGGTTG	84132
rs755659929	snp	A/C	1.65608e-05	0.00287752	missense	USP42	GRCh38.p7	7:6149725	GGTCAGTTAATAGGT[A/C]CTCAGTGATCCCAGA	84132
rs755666610	snp	C/G	1.65985e-05	0.00288079	intron-variant	USP42	GRCh38.p7	7:6145484	TGATCTGTGCCCTCG[C/G]AAATGTTTCTCCTGT	84132
rs755679367	snp	A/G	4.64123e-05	0.00481705	intron-variant	USP42	GRCh38.p7	7:6157063	TGGCCAGGGTAAGAG[A/G]AGATACTTGGAATTA	84132
rs755681301	snp	A/T	1.73788e-05	0.00294772	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116860	GAAAGTAGGGTGTGG[A/T]TGAAAACCCAGCACT	84132
rs755691419	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6101103	GAAAGGGCAGTGAAA[C/G]GAGTGGAGCAACAAT	84132
rs755694304	in-del	-/TATTACCTAGTTA	6.11527e-05	0.00552925	intron-variant	USP42	GRCh38.p7	7:6135987	TTTTATATTTGTATT[-/TATTACCTAGTTA]TACTTTTTTTTTTTT	84132
rs755698163	in-del	-/CTT			intron-variant	USP42	GRCh38.p7	7:6092124	TTCTTCTTCCTCTTC[-/CTT]CTTCTTCTTCTTCTT	84132
rs755704095	snp	C/T	1.91053e-05	0.00309068	missense	USP42	GRCh38.p7	7:6153962	CCGAGGAGCCTCCGC[C/T]CAGCGCCGGCGAGGA	84132
rs755717697	snp	A/G	1.96157e-05	0.00313169	synonymous-codon	USP42	GRCh38.p7	7:6155145	AAAGAAGCACAAAAA[A/G]TCAAAGAAGAAAAAG	84132
rs755741667	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6089298	ATCTTAGGTGATACA[C/G]CCACCTTGGCCTCCC	84132
rs755793000	snp	C/G	2.15098e-05	0.00327939	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111312	GACCAGTACCTGGTG[C/G]TGTAGTTTATTCGAG	84132
rs755813106	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6121349	CCTTGCATTCCTGAG[A/G]TGACTCACACTTGGT	84132
rs755818175	snp	C/T	1.65644e-05	0.00287783	synonymous-codon	USP42	GRCh38.p7	7:6150465	AATCTTAGAGACCTT[C/T]AGGCTTAGCAACAAA	84132
rs755821768	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6122538	GCAGTAGTGTGATCT[C/T]GGCTCAACTGCAACC	84132
rs755914183	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6079363	CGCTGGAGGCTGAGG[A/C]AGGAGAATCGCTTGA	84132
rs755928003	snp	A/T	3.31334e-05	0.00407009	missense	USP42	GRCh38.p7	7:6150476	CCTTCAGGCTTAGCA[A/T]CAAACTGAAAGGCTC	84132
rs755948932	snp	G/T	1.82734e-05	0.00302264	missense	USP42	GRCh38.p7	7:6154139	CGGCTCCGCCTGCGC[G/T]GTCGGAGGAGCCCTG	84132
rs755987079	snp	A/G	3.54302e-05	0.00420878	intron-variant	USP42	GRCh38.p7	7:6139204	CAATAAGTAAGTACA[A/G]CAGAGCGCCAGCCAT	84132
rs756010608	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6112663	GGCTTAGAGCATGCA[G/T]CCCAGACAGCTTTGA	84132
rs756010882	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6083474	TCAACCAGGCTGGTC[C/T]CAAACTCCTGACCTC	84132
rs756028475	snp	C/T	1.97e-05	0.00313841	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111202	TCAGCCTGGCAGCTC[C/T]GAGGCAGTCTCACCT	84132
rs756038751	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6078373	TTTGGGAGGCTGAGG[C/T]GGGCAGATCATTAGG	84132
rs756054891	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130366	CCCACATGGTCTCCA[C/T]GGACACTGCAGTGGG	84132
rs756058666	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6145275	GGCGGAGCTTCCAGT[A/G]AGCTGAGATCGTGTC	84132
rs756076675	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6146497	AGTGAGACCACATGT[C/G]TACAAAATACGAAAA	84132
rs756078242	snp	A/G	1.86093e-05	0.0030503	intron-variant	USP42	GRCh38.p7	7:6140041	AATTCTTGATCTTTT[A/G]TGAGCTCCCATGTGT	84132
rs756093978	snp	C/T	1.65622e-05	0.00287764	missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115437	AGAATTTGGGCAATA[C/T]CTGTTTTGCCAATGC	84132
rs756121039	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6117827	TTTTCTTTTTTGTTT[C/T]GTTTTTGTTTTGAAC	84132
rs756122796	snp	C/T	0.000486184	0.0155838	missense	USP42	GRCh38.p7	7:6153830	GCCCCGCCGCCGAAT[C/T]CCTGGAGGAGCCAGA	84132
rs756155582	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6116223	TACATGCTTATAAGC[C/T]TTAGAGGAGAGGGAC	84132
rs756212841	snp	C/T	6.62778e-05	0.00575626	synonymous-codon	USP42	GRCh38.p7	7:6149900	ACAGTCTACCTCGAA[C/T]GCATCTACGATGTCA	84132
rs756246116	snp	G/T	2.11754e-05	0.00325381	missense	USP42	GRCh38.p7	7:6156776	CAGGACTCAGACCTC[G/T]CAGCAGCGTGCTCTG	84132
rs756281181	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6138840	ATTTCATCCCAACCC[C/G]CTCTTCTGGTCTGTG	84132
rs756284840	snp	A/G	8.80993e-05	0.0066364	synonymous-codon	USP42	GRCh38.p7	7:6154245	ACCCGAGGCCGCAGA[A/G]CGGCCGCCAGCTCCT	84132
rs756292067	snp	C/G	1.67069e-05	0.00289019	intron-variant	USP42	GRCh38.p7	7:6142919	GTGGTGTTTGTGCCT[C/G]TTCTCTTCCCAGGCT	84132
rs756316470	snp	A/C	3.31967e-05	0.00407397	intron-variant	USP42	GRCh38.p7	7:6150540	TGAGGCACGTGTGGC[A/C]GCATAGTAGGAAATC	84132
rs756334587	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6106639	GCGCAGTTGTAGCTC[A/G]CTGTAGCCTCAATCT	84132
rs756345033	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6128943	CTCCTGCCTCAGCCC[C/T]GCAAGTGGCTTGGAC	84132
rs756379179	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6093724	TTACTTTTTTGTGGT[A/G]AAATATGGTAGGTAC	84132
rs756391606	snp	A/G	3.31263e-05	0.00406965	missense	USP42	GRCh38.p7	7:6149868	GTTCCCTCTTCTACC[A/G]TTACCAATTCTGCAG	84132
rs756394038	snp	A/G	1.65726e-05	0.00287855	missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115328	ATTTTTCTAGCCCTA[A/G]GTGATGGCATCGCTC	84132
rs756403539	in-del	-/C	1.65759e-05	0.00287883	intron-variant	USP42	GRCh38.p7	7:6159435	AAATCTCTTTCCTGA[-/C]CCTTTGCTTTCTAGG	84132
rs756427618	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6122952	CCTCAGCCTCCTGAG[C/T]AGCTGGGATTACAGG	84132
rs756432614	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098007	ACTCCCTGGTTTAAG[C/T]GATTCTCCTGCCTCA	84132
rs756442609	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6139640	CTCAAGAGGAAGAAC[A/G]AGGGGACAGATAATG	84132
rs756462522	snp	C/G	0.000130642	0.00808109	missense	USP42	GRCh38.p7	7:6154780	GCCCGGGACTGGAAG[C/G]CCTTCCACGGCGGCC	84132
rs756488869	snp	A/T	0.000112657	0.00750439	missense	USP42	GRCh38.p7	7:6154199	GGGACCACGCCCGGG[A/T]CGCTCAGGACCCATC	84132
rs756518825	snp	C/G	2.64337e-05	0.0036354	synonymous-codon	USP42	GRCh38.p7	7:6154905	CCGCCCCAGCAGCCC[C/G]CGCGCAGGCGCGCCC	84132
rs756583514	snp	C/G	1.65707e-05	0.00287838	synonymous-codon	USP42	GRCh38.p7	7:6147826	CGTCATCAGTCAGCG[C/G]GTTGTCACCAACAAA	84132
rs756585345	snp	A/G	2.63633e-05	0.00363056	intron-variant	USP42	GRCh38.p7	7:6135821	TTTGCTAATTTGGAG[A/G]ATTATCATCTATCTT	84132
rs756601548	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137226	AAGCCACTGAAGATT[A/G]AAGAGGTCTTATATT	84132
rs756624628	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148634	CCTGTCGGGGCGAAC[A/G]GTAGTGAGCTAGTGT	84132
rs756679815	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6109619	GGCTGGTCTCGAACT[-/C]CTGGACTCAAGTGAT	84132
rs756697725	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6091618	ACCCCCATATTAATT[G/T]TATTCTTGTTTTTTT	84132
rs756710100	snp	A/G/T	0.000133321	0.00816359	missense	USP42	GRCh38.p7	7:6147783	TTACTCATCCCACCC[A/G/T]TAGCCCCGGCCAGTC	84132
rs756710447	snp	A/G	1.67472e-05	0.00289367	synonymous-codon	USP42	GRCh38.p7	7:6150206	CGACAGTGACCCGAA[A/G]GAAAACGGCCTAGCG	84132
rs756733149	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6143624	ACCAGAGGGATTTTG[C/G]CTTTGTTTTAAATTC	84132
rs756785346	snp	C/G	7.68669e-05	0.006199	missense	USP42	GRCh38.p7	7:6155058	ACACGACAGTGTGGA[C/G]AACAGTGACAGTCAT	84132
rs756799439	snp	A/C	1.65605e-05	0.0028775	missense	USP42	GRCh38.p7	7:6149718	CAAAACTGGTCAGTT[A/C]ATAGGTCCTCAGTGA	84132
rs756806074	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6126852	TATATAGCTCTTTTT[C/G]TCAGCATGTCTTCAT	84132
rs756824398	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151493	ACCAGGCTGGAGTAC[A/G]GTGGTGCGATCTCAG	84132
rs756830613	snp	C/T	3.10169e-05	0.00393795	intron-variant	USP42	GRCh38.p7	7:6144044	CACAAATTGTGTGTA[C/T]ATATTCGTCTTCTTA	84132
rs756834007	snp	A/G	1.68692e-05	0.00290419	intron-variant	USP42	GRCh38.p7	7:6150375	AGGAGGCATGGAGCT[A/G]GCGACTGAAGCTGAA	84132
rs756854020	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6143096	TTGAGAGAGTTTGGT[A/G]TGTCTAGGTTGCTTG	84132
rs756905180	snp	A/G	0.000167224	0.00914243	missense	USP42	GRCh38.p7	7:6154985	TTGTAGCCGGAGACA[A/G]CTGTAACCTCTCTGA	84132
rs756923941	snp	C/T	1.68026e-05	0.00289845	synonymous-codon	USP42	GRCh38.p7	7:6149594	CCAGAATCCACCTCA[C/T]TTAAATGGGACTGGA	84132
rs756930219	snp	A/C			upstream-variant-2KB	USP42	GRCh38.p7	7:6077104	GGTCTTGAACTCCTG[A/C]TCTTGTGATCTGCCC	84132
rs756941504	snp	G/T	1.9845e-05	0.00314994	intron-variant	USP42	GRCh38.p7	7:6140029	CTGTCCTGTTTGAAT[G/T]CTTGATCTTTTGTGA	84132
rs756951530	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6108821	GCCATTTCTACTCCA[G/T]AGTTTTTTAAGGATC	84132
rs756951705	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6119888	TTTTGTTTTTTTGTA[C/G]AGACAGTCTCACCAT	84132
rs756969872	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6102450	CTGGAGGGACCAGTT[C/T]GTCAACAGCGTGAAA	84132
rs756996497	snp	C/G	1.94539e-05	0.00311875	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111195	ATCAGAATCAGCCTG[C/G]CAGCTCCGAGGCAGT	84132
rs757022903	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6100155	ACCGCACCTGGCCCA[A/G]TTTCACAGTTCTAAT	84132
rs757067053	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6146699	AACTCTGCCATGTGC[C/T]TGGAGAGTAAGAAAG	84132
rs757082336	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6112962	ATTCTGGAATGCAGT[C/G]GCGCGATCTCGGCTC	84132
rs757112958	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081152	CGTGCTGCGACTGTC[A/G]TCTTTCAGATCAGAG	84132
rs757117565	snp	C/G/T			intron-variant	USP42	GRCh38.p7	7:6102333	TGGCCAGGCTGGTCT[C/G/T]GAACTCCTGATCTTG	84132
rs757160153	snp	A/G	1.67506e-05	0.00289396	missense	USP42	GRCh38.p7	7:6149949	AAACCGATCCCCCGC[A/G]GTGAATCCTGCTCCC	84132
rs757166091	snp	C/T	0.000101415	0.00712019	synonymous-codon	USP42	GRCh38.p7	7:6154590	CCCTGGCGAGCGCCG[C/T]TCTCTGGGCAGGTGC	84132
rs757177989	snp	A/G	2.42081e-05	0.003479	synonymous-codon	USP42	GRCh38.p7	7:6139147	CCATGAATTCCTTCA[A/G]TACACTGTTGATGCT	84132
rs757202150	snp	C/G	4.10458e-05	0.00453004	intron-variant	USP42	GRCh38.p7	7:6145664	ACATAAAAGTAAGCT[C/G]TGCAGATTTGCTATT	84132
rs757204219	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6159295	CAGCCGCTGAGCGCT[C/G]GGACATCCCTGCTCA	84132
rs757217576	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095024	AACTCCTAACCTCAA[A/G]GGATCTGCCCGTCTG	84132
rs757238382	snp	A/G			missense	USP42	GRCh38.p7	7:6150135	GAAGATGAGGAGGCC[A/G]CTCCGCACGAGCTTC	84132
rs757241741	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6086129	CAACCTTCGCCTCAC[A/T]GGTTCAAGCAATTCT	84132
rs757247997	snp	A/G	4.71999e-05	0.00485775	intron-variant	USP42	GRCh38.p7	7:6146144	TATTGGCTCTCATTT[A/G]TAGGCTAGCAATGGC	84132
rs757265981	snp	G/T	4.67475e-05	0.00483442	intron-variant	USP42	GRCh38.p7	7:6135981	TTGTAGTTTTATATT[G/T]GTATTTATTACCTAG	84132
rs757271216	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6107700	AGGTGTGAGCACCTG[A/C]GCCCGGCCTCTTCTT	84132
rs757301166	in-del	-/CGCGACCGC	2.13856e-05	0.00326991	cds-indel	USP42	GRCh38.p7	7:6154515	ACCTGCCCCCGGGAG[-/CGCGACCGC]CGCGACCGCCAGGAC	84132
rs757330781	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6092054	TCTTCTTCTTCTTCT[-/C]TTCTTCTTCTTCTTC	84132
rs757387218	snp	C/T	1.70081e-05	0.00291612	intron-variant	USP42	GRCh38.p7	7:6140993	GATAAAGGTAAATTT[C/T]ATAATTATGGGAGTA	84132
rs757387275	snp	A/C	2.03461e-05	0.00318946	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111373	ACCACAAAAGGATCA[A/C]GGTACTGTTTTTCAA	84132
rs757405723	snp	C/T	1.65721e-05	0.0028785	synonymous-codon	USP42	GRCh38.p7	7:6145587	AGAGCCAATTGTCTA[C/T]GTCTTGTATGCAGTG	84132
rs757405856	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6155458	AAATGATAGTGCCAT[G/T]TTTGGTGAATGCTTT	84132
rs757418213	snp	A/G	1.87778e-05	0.00306407	missense	USP42	GRCh38.p7	7:6154769	CCCTGTACGCTGCCC[A/G]GGACTGGAAGCCCTT	84132
rs757436984	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6129139	TCACTTTTAGGGACC[A/G]CATTTACACACACAT	84132
rs757444090	snp	A/T	0.000101779	0.00713298	missense	USP42	GRCh38.p7	7:6147768	AAAATGGAGGTGAAC[A/T]TACTCATCCCACCCA	84132
rs757451725	snp	A/G	1.65712e-05	0.00287843	missense	USP42	GRCh38.p7	7:6147822	GCCCCGTCATCAGTC[A/G]GCGGGTTGTCACCAA	84132
rs757454085	snp	C/T	1.84378e-05	0.00303621	synonymous-codon	USP42	GRCh38.p7	7:6154155	GTCGGAGGAGCCCTG[C/T]GAGCAGCCACTCCTT	84132
rs757469674	in-del	-/T			upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081192	TCTGGTGGGAGTGTC[-/T]TTCCCCCGACACCCC	84132
rs757475270	snp	A/C	1.66037e-05	0.00288125	intron-variant	USP42	GRCh38.p7	7:6140230	TTGATAAAATGATAC[A/C]CACATGTGGTTAAAA	84132
rs757492908	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6121405	TGGCTTTGATTTGCT[A/G]AAATTGTAAAACAGT	84132
rs757522143	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6095810	GGTCTCACTGTTACC[C/T]GGGCTGCAGTGGTGT	84132
rs757533228	snp	C/G			missense	USP42	GRCh38.p7	7:6154444	CGCTCGTCCAGCGGG[C/G]AGCCCGCCAGAGAGA	84132
rs757579160	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6123741	TAGTCTTAGCTACTC[A/G]GGAGGCCGAGGTAGG	84132
rs757580252	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6116268	CCGCAACCTCCTGGA[A/T]TTCAGACTAGACTTT	84132
rs757590880	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151749	TGCCCGGCCAGCAGA[A/G]TCGTTTATTGCCATT	84132
rs757604634	snp	C/G	2.04e-05	0.00319368	synonymous-codon	USP42	GRCh38.p7	7:6157051	TCTCTTTGAGTATGG[C/G]CAGGGTAAGAGGAGA	84132
rs757620872	snp	G/T	3.80322e-05	0.00436058	missense	USP42	GRCh38.p7	7:6154712	AGTTCTACCCCGACA[G/T]GCCGCGCTGGGACAG	84132
rs757635841	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6086687	TTCCCTTCCCCCTTC[A/C]CTTTCCCCTTTCCTT	84132
rs757667924	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6117737	TCAGTTTTAGCCATC[-/T]CCATAGGTGTGTAGT	84132
rs757673416	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6157955	GTGACCGCTCACCCT[C/T]GAGAGGAGCTGTGAG	84132
rs757691271	snp	G/T	1.96636e-05	0.0031355	missense	USP42	GRCh38.p7	7:6144179	TTTGCAAATTTTACC[G/T]GTGGAAAAATTGCTA	84132
rs757708536	snp	A/G	1.84742e-05	0.0030392	synonymous-codon	USP42	GRCh38.p7	7:6150122	CGGCCAAGATGCCGA[A/G]GATGAGGAGGCCACT	84132
rs757734114	in-del	-/G	1.76457e-05	0.00297028	frameshift-variant	USP42	GRCh38.p7	7:6157008	AAACGAAACACTTAC[-/G]GATGGAAAGCAGGGA	84132
rs757738350	snp	A/T	6.95132e-05	0.00589506	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116840	CTATCACTTTTGCGC[A/T]TAATGAAAGTAGGGT	84132
rs757741359	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6117385	GTAGCATCACTTGAT[C/G]GTATTGTTGAGTAGG	84132
rs757759781	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120173	GTTTCACTGTGTTAG[C/T]CAGGATGGTCTTGAT	84132
rs757761310	snp	A/G	5.21354e-05	0.00510539	intron-variant	USP42	GRCh38.p7	7:6116771	ATTAACGTTCTGTTT[A/G]CCCTCATTTTCTCCC	84132
rs757781425	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6102658	ACTGTGGGCTGCGCA[C/G]AAGAGGCAGCATGGG	84132
rs757783761	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6097387	GGTCCCTGTGGGTCC[-/T]TTTTTTTTTTTTTTT	84132
rs757801310	snp	A/C	9.46507e-05	0.00687869	missense	USP42	GRCh38.p7	7:6153918	CCCCGCTACCAAAGA[A/C]GGCGCCTGGGAGGCC	84132
rs757832805	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6149506	GCAAAATGGGAAGGA[C/T]CCATCAGCCAAAATG	84132
rs757839770	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6125812	CTTTGTTGTTGATTT[C/T]AGTTTTTGTTTTTTT	84132
rs757877951	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6109794	CAACTTCTGTCTCCC[A/G]GGTTCAAGCGATTTT	84132
rs757894656	snp	C/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077912	CAGGCTGGTCTCGAA[C/G]TGCTGACCTCATGAT	84132
rs757945954	snp	A/C			upstream-variant-2KB	USP42	GRCh38.p7	7:6077152	TGCTGGGATTACAGG[A/C]GTGATGAGCCACCGT	84132
rs757957010	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6111055	AATGATCTTCCAAGA[C/T]CTAACGGTAGGGTAA	84132
rs757962308	snp	A/C			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161656	TAAAACCTTCAAGTA[A/C]GTGCTCCTGCCGAAG	84132
rs757974351	snp	C/G	1.6898e-05	0.00290667	intron-variant	USP42	GRCh38.p7	7:6150370	ATTTCAGGAGGCATG[C/G]AGCTGGCGACTGAAG	84132
rs757978898	snp	A/T	0.000124278	0.00788184	missense	USP42	GRCh38.p7	7:6154922	GCGCAGGCGCGCCCC[A/T]CGCCCTCGCCCCGCA	84132
rs757994464	snp	A/G	1.6937e-05	0.00291002	intron-variant	USP42	GRCh38.p7	7:6147910	AACAGTCCTTAGGGA[A/G]AAGAACATTTTTATG	84132
rs758007295	snp	C/G	1.76608e-05	0.00297155	missense	USP42	GRCh38.p7	7:6154058	CGTTGTCCCAGGACG[C/G]AAAGGGGATGATCGC	84132
rs758090311	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104427	GGCTGCGTCCGCTAG[A/G]CCAAGGGAGGCGCAA	84132
rs758101645	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6098095	ATTTTTAGTAGAGAC[A/G]GGTTTCACCATGTTG	84132
rs758122731	snp	C/T	3.42965e-05	0.0041409	missense	USP42	GRCh38.p7	7:6156839	AAGAAAAAGAAGAGA[C/T]ATTCAAGAAAATCAG	84132
rs758160234	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161837	GCAAGAGCTCTGACA[A/G]CCATCCACCCTCCAA	84132
rs758188911	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6159905	CGTCCGTCCCGTCCC[-/CT]GTGCTGCTGTCTGCG	84132
rs758207042	snp	A/G	2.09172e-05	0.00323391	missense	USP42	GRCh38.p7	7:6154523	CCCGGGAGCGCGACC[A/G]CCAGGACCGCCACGC	84132
rs758207984	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6088082	AGGCAGGAGGATTGC[G/T]TGAGGCCAGGAGTTC	84132
rs758213545	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137390	TTGAGATGGAGTCTC[A/G]CTCTGTCCCCAAGCC	84132
rs758291035	snp	C/T	0.000342642	0.0130845	synonymous-codon	USP42	GRCh38.p7	7:6153825	TGGCAGCCCCGCCGC[C/T]GAATCCCTGGAGGAG	84132
rs758292198	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6091936	TTTTTCTATTCGATA[C/T]CTGCCTGGAAAAAAT	84132
rs758308318	snp	C/T	3.42161e-05	0.00413605	synonymous-codon	USP42	GRCh38.p7	7:6145626	CACTGGTTTTAATTG[C/T]CATGCTGGCCATTAC	84132
rs758322239	snp	C/T	1.65734e-05	0.00287862	missense	USP42	GRCh38.p7	7:6147849	CCAACAAACAGGCTG[C/T]GCCAGGCTTTATCGG	84132
rs758331217	in-del	-/CA			upstream-variant-2KB	USP42	GRCh38.p7	7:6078601	AGCAAGACTCCATCT[-/CA]AAAAAAAAAAAAAAA	84132
rs758334710	snp	G/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114893	GACGGGGTTTCACCT[G/T]GTTAGCCAGGATGGT	84132
rs758344882	snp	A/G	1.65633e-05	0.00287774	missense	USP42	GRCh38.p7	7:6149824	AACCTAACCTTCATA[A/G]TAATTCTTTGGAGAA	84132
rs758353005	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6152280	TCATCAGGAAGTCGT[C/G]TTCTCATGGCGAACA	84132
rs758374123	snp	G/T			intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153394	TGTTTTGAAAAATAG[G/T]CTAGGAGCTGGGCTT	84132
rs758374921	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138516	AACTTGCTAGAAACA[C/T]GAGTCACTCTGTAGC	84132
rs758376385	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6155677	GCCTGCCCAGCGTAG[G/T]CATCGGAGACACCTT	84132
rs758409939	snp	G/T	4.95074e-05	0.00497506	intron-variant	USP42	GRCh38.p7	7:6156749	TCTGGCTTTTCCTTC[G/T]GCAGGCATCAGCAGG	84132
rs758433522	snp	C/T	3.3134e-05	0.00407012	intron-variant	USP42	GRCh38.p7	7:6145512	TGTTTCCATTTCCTT[C/T]TAGGATGTGAAATAC	84132
rs758441505	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6090169	GACAGGCATGGTGGC[A/G]CATGCCTGTAATCCC	84132
rs758473775	in-del	-/GTT			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114585	GTTCATATTTCTCTG[-/GTT]GTTGTTTTATGTATA	84132
rs758501562	snp	C/T	1.89392e-05	0.00307721	synonymous-codon	USP42	GRCh38.p7	7:6157039	TGACAGGTGTCGTCT[C/T]TTTGAGTATGGCCAG	84132
rs758513301	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6122210	TCCAATGTAAGTGTC[A/C]AATGCTATAAATTTC	84132
rs758514756	snp	A/G	1.72567e-05	0.00293735	missense	USP42	GRCh38.p7	7:6147752	AGGTCCCATGATGTG[A/G]AAAATGGAGGTGAAC	84132
rs758537358	snp	C/T	3.35773e-05	0.00409726	intron-variant	USP42	GRCh38.p7	7:6140069	TGTTTGAAATCTGGT[C/T]ACAGCATCTGGAGTT	84132
rs758541065	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6095967	ACAGAGTCTTACTGT[G/T]CTCAGGTTGGTCTCG	84132
rs758550048	in-del	-/GTG			intron-variant	USP42	GRCh38.p7	7:6129120	CCTGTAGCCTTTTTA[-/GTG]GTCACTTTTAGGGAC	84132
rs758566349	snp	C/G/T	5.51266e-05	0.00524984	missense	USP42	GRCh38.p7	7:6154150	GCGCGGTCGGAGGAG[C/G/T]CCTGCGAGCAGCCAC	84132
rs758566418	snp	A/G			intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6121564	AAGAGTTTGTACAGA[A/G]TTGATGTTATTTCTT	84132
rs758577862	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6147638	TGCTATTTTTTTCAT[C/T]AGGTTTCCGCCTGAG	84132
rs758584009	snp	A/G	0.000156479	0.00884393	missense	USP42	GRCh38.p7	7:6150054	TCTGACGAGGAGTCA[A/G]AGGGGCTGGGCAAGG	84132
rs758598561	snp	C/G	2.58068e-05	0.00359204	missense	USP42	GRCh38.p7	7:6154655	AGCTGGACTGGGTCA[C/G]ACACCACTACACCGA	84132
rs758621313	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120344	ACCTCTTCGGTTTAA[A/G]TGATTCTCCTGCCTC	84132
rs758644479	snp	C/T	1.7895e-05	0.00299118	intron-variant	USP42	GRCh38.p7	7:6147711	AGGTGTCCTGTGTCA[C/T]CCTAAGTATCGCTCT	84132
rs758661509	snp	C/T	5.21354e-05	0.00510539	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116831	ACAGCTTTCCTATCA[C/T]TTTTGCGCTTAATGA	84132
rs758662106	snp	C/T	0.000423908	0.0145525	missense	USP42	GRCh38.p7	7:6153884	CCAAGAAGGCTCCGC[C/T]GCCCCGCGATCCCGG	84132
rs758685919	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6112428	GCATTTCAGCCTGGG[C/T]AACAGAGTGAGACTC	84132
rs758745223	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6110271	GAACGCTGGACCTGG[C/T]TCTCAGTCCCAGTTG	84132
rs758774602	snp	C/T	8.66318e-05	0.00658091	intron-variant	USP42	GRCh38.p7	7:6149569	CTGACCAGGTGCGCT[C/T]TGCTTACTTCCAGAA	84132
rs758797462	in-del	-/G			frameshift-variant	USP42	GRCh38.p7	7:6153890	AGGCTCCGCCGCCCC[-/G]CGATCCCGGCACCCC	84132
rs758806375	snp	C/G	8.41786e-05	0.00648708	synonymous-codon	USP42	GRCh38.p7	7:6154344	GGACGCCGCGGCGCC[C/G]AAAGCCCCAGGCCCT	84132
rs758854151	in-del	-/AAG	3.49815e-05	0.00418205	cds-indel	USP42	GRCh38.p7	7:6156830	AAAAAGAAGAAGAAA[-/AAG]AAGAGACATTCAAGA	84132
rs758855980	snp	A/T	1.70496e-05	0.00291967	missense	USP42	GRCh38.p7	7:6153910	CCCGGCACCCCCGCT[A/T]CCAAAGAAGGCGCCT	84132
rs758871205	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6107798	AGGAAAAATGTAAAC[C/T]GTATTTGGAGGATAA	84132
rs758878074	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6087913	TTTTATCTGCTTTGT[A/G]GTCGTGTTGCAAACA	84132
rs758884605	snp	A/T	1.65803e-05	0.00287922	synonymous-codon	USP42	GRCh38.p7	7:6142955	GAGTGTCAACAAGGC[A/T]TTGGAGCAGTTTGTG	84132
rs758892492	in-del	C/TTTTTTTTTT			intron-variant	USP42	GRCh38.p7	7:6089215	CGCCTGGCTAATTTT[C/TTTTTTTTTT]GTATTTTTAGTAGAG	84132
rs758926957	snp	A/G	5.38517e-05	0.00518874	missense	USP42	GRCh38.p7	7:6154300	CACCCGGAAGGGGAC[A/G]CTGAGCCTAGCCCCG	84132
rs758935843	snp	C/T	6.68975e-05	0.0057831	synonymous-codon	USP42	GRCh38.p7	7:6156913	CAGCTTGGAGACTGT[C/T]GCCCAGTTCCGGAGA	84132
rs758985742	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6121908	TCAAATGATCCTCCC[C/T]GCTTGGCCTCCAAAA	84132
rs758996287	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6140525	TCCCCTATCGATGGG[A/T]TTTAGGTTGTTTGTG	84132
rs759014605	snp	C/T	0.000419199	0.0144715	synonymous-codon	USP42	GRCh38.p7	7:6154575	CGGCGACAGGCTCAG[C/T]CCTGGCGAGCGCCGC	84132
rs759035709	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130783	GAGACACAAGAGAGG[C/T]TCAGGAAGACAAAGA	84132
rs759051939	in-del	-/CACATACA			intron-variant	USP42	GRCh38.p7	7:6091683	TTATGTTAGCATACA[-/CACATACA]CACACACACACACAC	84132
rs759086794	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6085338	CACCACTTTGGCCAC[A/G]CTGGTCTGGATCTCC	84132
rs759104089	snp	A/G	3.37496e-05	0.00410775	missense	USP42	GRCh38.p7	7:6154622	GTCACCACCACTCCC[A/G]ACACCGGAGCGGGGT	84132
rs759139011	snp	A/G	1.77865e-05	0.0029821	synonymous-codon	USP42	GRCh38.p7	7:6156823	ACACAAAAAAAAGAA[A/G]AAGAAAAAGAAGAGA	84132
rs759165525	in-del	-/A			frameshift-variant	USP42	GRCh38.p7	7:6156812	GACCTCCACAGACAC[-/A]AAAAAAAGAAGAAGA	84132
rs759192880	snp	A/G	9.98918e-05	0.00706653	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115284	TTAGCTTCAGTATGC[A/G]AAGCTTGGTTTCTGA	84132
rs759195725	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6119687	ATTCATTTAGGCCTT[G/T]TTTTTTGTTGTTGTT	84132
rs759211110	snp	A/G	1.65638e-05	0.00287778	missense	USP42	GRCh38.p7	7:6149871	CCCTCTTCTACCATT[A/G]CCAATTCTGCAGTAC	84132
rs759211169	snp	A/C	1.79181e-05	0.00299311	missense	USP42	GRCh38.p7	7:6153867	CGCCGGCCTCAGCAG[A/C]ACCAAGAAGGCTCCG	84132
rs759215969	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6147127	TATTAAACACTGGCA[C/T]TGGATTTCGGCAGTT	84132
rs759227979	snp	C/T			utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081776	CGGGCCGCTCCTCCC[C/T]GCTGTTCACGAGGAA	84132
rs759232416	snp	A/G	2.25594e-05	0.00335845	missense	USP42	GRCh38.p7	7:6154228	TCCCAGAGCTTGGGC[A/G]CACCCGAGGCCGCAG	84132
rs759247262	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6135781	CTGATTTGTAATTAG[A/C]CTTGATGTGTGTATA	84132
rs759252037	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6159870	GGCACCTCACTCAGG[A/G]GAGCGGAGCCTTGCT	84132
rs759259161	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6139389	TACACGTGTGTCTTA[C/G]GTAACAGTTTGAGTT	84132
rs759307000	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6146384	TCAACTCTAGCCTGG[A/G]CATGGTGCCTCACGC	84132
rs759332445	snp	C/T	4.96989e-05	0.00498467	intron-variant	USP42	GRCh38.p7	7:6140099	TTTTGCAAAGCTCTT[C/T]TCTCATGTCACTGTT	84132
rs759350212	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6106451	CATTTGATAACAAGG[A/G]AGACATACCATATAA	84132
rs759424872	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096172	ACAACCAGGTTATTA[C/T]AGACATATAGGTATA	84132
rs759443056	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6149335	CAGAACGAGTTTGGT[C/T]GGAGGATTGTTTTCT	84132
rs759456118	snp	C/T	3.31444e-05	0.00407076	synonymous-codon	USP42	GRCh38.p7	7:6147814	CTCTCCCCGCCCCGT[C/T]ATCAGTCAGCGGGTT	84132
rs759472526	snp	A/G	4.34849e-05	0.00466268	missense	USP42	GRCh38.p7	7:6153820	CAGCCTGGCAGCCCC[A/G]CCGCCGAATCCCTGG	84132
rs759491704	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130109	TCTTGCGTCGACCTC[C/T]GAAAGTGCTAGAATT	84132
rs759500726	snp	A/C	1.68601e-05	0.00290341	missense	USP42	GRCh38.p7	7:6140970	CCATATCTTGATATA[A/C]CATTGGAGATAAAGG	84132
rs759545822	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6157486	CACTGCAACCTCTGC[C/G]TCCCAGGTTCATGCT	84132
rs759556002	in-del	-/TTT			intron-variant	USP42	GRCh38.p7	7:6092053	TTCTTCTTCTTCTTC[-/TTT]TTTCTTCTTCTTCTT	84132
rs759561975	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6133973	TCAGCTCACTGCAAG[C/T]TCTGCTTCCTGGGTT	84132
rs759598164	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6098828	TGGGATTACAGGCAT[A/G]AGCCACCATGCCCTG	84132
rs759610637	snp	C/T	0.000240394	0.0109608	synonymous-codon	USP42	GRCh38.p7	7:6154335	GAGGGTCGAGGACGC[C/T]GCGGCGCCGAAAGCC	84132
rs759615539	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6133057	TTTCTTCATGTTTCT[A/C]CTCCTGGAATTTGTT	84132
rs759665713	snp	G/T	1.65605e-05	0.0028775	missense	USP42	GRCh38.p7	7:6149677	GTGTCAACAGGGCTA[G/T]TCCTGTTAATGCTTC	84132
rs759675721	snp	A/G	1.84035e-05	0.00303338	synonymous-codon	USP42	GRCh38.p7	7:6157030	AAGCAGGGATGACAG[A/G]TGTCGTCTCTTTGAG	84132
rs759680865	snp	C/T	2.14268e-05	0.00327306	missense	USP42	GRCh38.p7	7:6153946	GCCATGGCCGTCGCC[C/T]CCGAGGAGCCTCCGC	84132
rs759722310	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6110273	ACGCTGGACCTGGCT[C/G]TCAGTCCCAGTTGCT	84132
rs759750226	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6138710	CCTCCTGTCAGATCA[A/G]TGGCAGCATTAGATT	84132
rs759751853	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6106135	TTTAAATTAGGGTCA[G/T]TTTCACTTTCTCTTC	84132
rs759757244	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6139781	TGGGTCGGAGGAAGA[-/CT]CTCTGCCTTTTCCGC	84132
rs759763185	snp	C/T	3.48335e-05	0.00417319	synonymous-codon	USP42	GRCh38.p7	7:6155097	GAAAGCCCGGAGGAG[C/T]GAACAGAAGGATCCT	84132
rs759808953	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6122004	AGTTTTTTAATGTTA[C/T]TGATCTTCTCAAAGA	84132
rs759821528	snp	A/G	1.66535e-05	0.00288556	intron-variant	USP42	GRCh38.p7	7:6143026	GCAAGTACGTTGGGT[A/G]GTGACTTGATTCTTG	84132
rs759827661	snp	G/T	7.28558e-05	0.00603511	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111155	ATAGTTGACAAAGCT[G/T]CTGAATCTTCAGACC	84132
rs759837342	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6158442	TTTTGCTTCTCGGCT[C/G]AGTTGTGGGTTAGGT	84132
rs759841484	snp	C/T			utr-variant-3-prime	USP42	GRCh38.p7	7:6161144	CAGTTATGATGAGTA[C/T]TTACATTATGAATGT	84132
rs759845063	snp	A/T	1.8932e-05	0.00307663	synonymous-codon	USP42	GRCh38.p7	7:6144103	TAAAAAGATGGTTCC[A/T]GCTTCAAAGAGGTTC	84132
rs759849327	in-del	-/TTCT	2.86611e-05	0.00378546	intron-variant	USP42	GRCh38.p7	7:6144054	GTGTATATATTCGTC[-/TTCT]TATACTTTTGTTTCT	84132
rs759862213	snp	C/T	1.6569e-05	0.00287824	missense	USP42	GRCh38.p7	7:6150424	CAGTTGATGCCTGCT[C/T]CTTTGCTGTCTCTCC	84132
rs759876485	snp	A/G	1.69723e-05	0.00291305	synonymous-codon	USP42	GRCh38.p7	7:6155037	TGGAAAGTCCCGGAA[A/G]CGGAGACACGACAGT	84132
rs759879389	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6146727	AAGGTAGTGTCTGAG[C/T]GGGATGATGAGTTTG	84132
rs759918912	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6119569	ATTTCTACAAATAAT[C/G]TTCCTGGTATTTTGA	84132
rs759969689	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6151921	TGTGATCTTATGGAC[C/T]GCCATCATATGTGGT	84132
rs759988693	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6109431	AGGCAGAGTCTCTCT[A/G]TGTCAGTCTGGAGTG	84132
rs760002991	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152558	GCGTAGATATTAAAC[C/T]GGAATGGGGCGAACC	84132
rs760024453	snp	A/G	1.78042e-05	0.00298359	synonymous-codon	USP42	GRCh38.p7	7:6154095	CCCGCGGGACTCGGC[A/G]TTGGCGGAAGCCCCG	84132
rs760060676	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6137086	AGTAAACTTTTGCAT[C/G]TTGTTAATTGAGTTG	84132
rs760083951	snp	A/G	3.97907e-05	0.00446024	intron-variant	USP42	GRCh38.p7	7:6146263	GGTATTGTCATGAAA[A/G]CAAATTGCCAGATTT	84132
rs760090813	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120200	TGATCTCCTGACCTC[A/G]TGATCTGCCTGCCTC	84132
rs760092570	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103845	AGCTGCTTGAGCCCA[A/G]GAATCTTAGACCTGC	84132
rs760110571	snp	G/T	4.60713e-05	0.00479932	intron-variant	USP42	GRCh38.p7	7:6139228	CAGCCATGTCTTCAT[G/T]GGGGATCTCTGGTTG	84132
rs760112303	snp	C/G	1.87096e-05	0.0030585	intron-variant	USP42	GRCh38.p7	7:6150344	TCGTTTGTGGCGGTT[C/G]CCTTGGCTGGATTTC	84132
rs760122443	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114381	AAGAGTAATTATAAT[A/G]AACTCTCATGTAGCC	84132
rs760143928	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6125459	CACACCACTGCACTC[C/G]AGCCTAGGCAACAAG	84132
rs760150770	snp	A/T	0.000537252	0.016381	intron-variant	USP42	GRCh38.p7	7:6156720	TGGTGGTTTTGTGTT[A/T]TAGGGTTTTGAATTC	84132
rs760172830	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6122699	TGGTCTCTTATCTCC[C/T]GGCCTTGTGATCCAC	84132
rs760175706	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6111882	CGTCCTGAAGTGCTG[A/G]GATTACAGGCATGAA	84132
rs760194742	snp	A/G	1.65622e-05	0.00287764	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115354	CGCTCCTCCACAGAA[A/G]GTTCTTTTCCCATCT	84132
rs760236752	snp	C/T	1.93302e-05	0.00310882	missense	USP42	GRCh38.p7	7:6156803	TCTGACGCTGACCTC[C/T]ACAGACACAAAAAAA	84132
rs760240237	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6144951	TCACTTAATATAGAT[C/G]CTGACTTGTTAAAAG	84132
rs760268924	snp	G/T	0.000242689	0.011013	missense	USP42	GRCh38.p7	7:6153811	GCCGAGCCTCAGCCT[G/T]GCAGCCCCGCCGCCG	84132
rs760294309	in-del	-/T	1.70203e-05	0.00291716	intron-variant	USP42	GRCh38.p7	7:6147917	TTAGGGAGAAGAACA[-/T]TTTTTATGTTAATTT	84132
rs760295336	snp	A/G			downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161538	GCATGTAAAATTTCT[A/G]TAGTATATAAATGGC	84132
rs760312724	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6159865	GCACAGGCACCTCAC[G/T]CAGGAGAGCGGAGCC	84132
rs760316781	snp	A/G	1.65784e-05	0.00287905	intron-variant	USP42	GRCh38.p7	7:6150516	AATGAGGTAACGTAA[A/G]AGTACATCTGAGGCA	84132
rs760339142	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103122	TCATGGTGGAGGGGA[A/G]ATGCAGAGATGAACT	84132
rs760341494	snp	C/T	5.05565e-05	0.0050275	synonymous-codon	USP42	GRCh38.p7	7:6140936	TTTAAATTGCAAGGG[C/T]GTTTCAGATACTTTT	84132
rs760380793	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6126706	CTAGTTTTGGGATAT[A/C]GTGAGTAGAGCTGCA	84132
rs760402943	snp	A/G	3.31252e-05	0.00406958	synonymous-codon	USP42	GRCh38.p7	7:6149810	CCAGTGTCAGTCTCA[A/G]CCTAACCTTCATAGT	84132
rs760442443	snp	A/T	1.65861e-05	0.00287972	intron-variant	USP42	GRCh38.p7	7:6140208	GAGGTAAGCTTTTGC[A/T]TATAAGTTGATAAAA	84132
rs760453786	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6108454	TATCCCTACTTCATA[G/T]CATGGGTAGTACTTT	84132
rs760486984	in-del	-/AA			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103739	GACCCCCGTCTCTAC[-/AA]AAAAAAAAAAAAAAA	84132
rs760491595	snp	C/T	1.6896e-05	0.0029065	intron-variant	USP42	GRCh38.p7	7:6157110	TTCTTAATACATTTT[C/T]TTTGCAAAGGTGATT	84132
rs760491665	in-del	-/GAAAG			intron-variant	USP42	GRCh38.p7	7:6160128	AACCATTTTTCCCTT[-/GAAAG]GAAAGGAAACTTTGT	84132
rs760509950	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6131882	CTCCCAGAAGTGCAA[C/G]TCTCATGTTTGTTTT	84132
rs760525737	snp	C/T	1.72116e-05	0.00293351	synonymous-codon	USP42	GRCh38.p7	7:6154743	GTGCCGGTACTACCA[C/T]GACAGGTACGCCCTG	84132
rs760534604	in-del	-/T	0.000235821	0.0108561	intron-variant	USP42	GRCh38.p7	7:6155236	AGGCGCTGGCGCTGC[-/T]TGTCAGCAGTGGGGC	84132
rs760551529	snp	A/G	1.89457e-05	0.00307774	missense	USP42	GRCh38.p7	7:6150115	ACTCTCCCGGCCAAG[A/G]TGCCGAAGATGAGGA	84132
rs760560585	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6141491	GTGAGCCACCGCGCC[C/T]GGCCTGAATTTTCAT	84132
rs760565253	snp	C/T	1.73815e-05	0.00294795	synonymous-codon	USP42	GRCh38.p7	7:6147745	TGTTTCCAGGTCCCA[C/T]GATGTGAAAAATGGA	84132
rs760570403	snp	C/T	1.6577e-05	0.00287893	missense	USP42	GRCh38.p7	7:6147806	GGCCAGTCCTCTCCC[C/T]GCCCCGTCATCAGTC	84132
rs760603796	snp	A/C	3.08809e-05	0.00392931	missense	USP42	GRCh38.p7	7:6154832	TGCACGAGCGGCCGC[A/C]CAAGGACCACAACCG	84132
rs760613273	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6078537	AACCCAGGAGGCAGA[A/G]CTTGCAGTGAGCCAA	84132
rs760613820	snp	A/G	3.70501e-05	0.00430391	missense	USP42	GRCh38.p7	7:6154186	GTTCACCCCAGCGGG[A/G]ACCACGCCCGGGACG	84132
rs760625109	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6124823	TGGCATATTTTTGAT[-/A]TTTTTTTTCATGGTG	84132
rs760641392	snp	A/C	1.71431e-05	0.00292767	missense	USP42	GRCh38.p7	7:6150159	GAGCTTCAAGAACCC[A/C]TGACCCTAAACGGTG	84132
rs760652427	snp	C/T	3.3961e-05	0.0041206	synonymous-codon	USP42	GRCh38.p7	7:6154704	CCGGGAGAAGTTCTA[C/T]CCCGACAGGCCGCGC	84132
rs760685330	snp	C/T	1.73999e-05	0.00294952	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116920	GACAAAATTCAGAAG[C/T]TCCCGATGTCCAGAA	84132
rs760719561	snp	C/T	4.54494e-05	0.00476683	missense	USP42	GRCh38.p7	7:6154285	ATGGCCCCGGCCGGT[C/T]ACCCGGAAGGGGACG	84132
rs760724122	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096334	CAAAGCAGAGTCTCC[C/T]CAAGGGAAAGTGACA	84132
rs760726077	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080924	GTGTAATGTTTACAG[C/T]GAATTCTGCCACTGC	84132
rs760751789	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6124792	TTGATATATGATTTT[A/G]TTTAATCTGCTTCAT	84132
rs760770772	snp	A/T	1.71546e-05	0.00292865	synonymous-codon	USP42	GRCh38.p7	7:6154965	CTCCCACGACAGAAC[A/T]GCACTTGTAGCCGGA	84132
rs760807175	snp	G/T	0.000118476	0.00769572	synonymous-codon	USP42	GRCh38.p7	7:6153879	CAGCACCAAGAAGGC[G/T]CCGCCGCCCCGCGAT	84132
rs760809771	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6088675	CATCGATCTTTCACC[A/G]TTAGAATCTCCCTAA	84132
rs760814900	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6135108	ACAGTGATGTCTCAT[C/T]CCTGCTGTGGGAGAC	84132
rs760871821	in-del	-/TC			intron-variant	USP42	GRCh38.p7	7:6092052	TCTTCTTCTTCTTCT[-/TC]TTTCTTCTTCTTCTT	84132
rs760913096	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6141258	CCCAGGCTGGCATGC[A/G]GTGGCGTGATCTCGG	84132
rs760963473	snp	A/G	1.66682e-05	0.00288684	missense	USP42	GRCh38.p7	7:6147887	CTTCCCTCTCACATG[A/G]TAAAGGTAACAGTCC	84132
rs760963603	snp	A/G	3.81461e-05	0.0043671	intron-variant	USP42	GRCh38.p7	7:6150331	AGGGTCTTCAGCCTC[A/G]TTTGTGGCGGTTCCC	84132
rs760965341	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6140322	CCCAGATTCTCATTC[C/G]TTTTACCCAGAGGCA	84132
rs760968519	snp	C/T	0.000111383	0.00746186	intron-variant	USP42	GRCh38.p7	7:6139052	AACTTAGGCTTATTA[C/T]GTGTAATGATAAAGC	84132
rs760978936	snp	A/G	1.74659e-05	0.0029551	intron-variant	USP42	GRCh38.p7	7:6149560	TCTGGAGCTCTGACC[A/G]GGTGCGCTCTGCTTA	84132
rs760985670	snp	C/T	1.77621e-05	0.00298006	synonymous-codon	USP42	GRCh38.p7	7:6154089	GGAGGGCCCGCGGGA[C/T]TCGGCGTTGGCGGAA	84132
rs761005836	snp	C/G/T	3.64121e-05	0.00426673	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111144	GAACAATGACCATAG[C/G/T]TGACAAAGCTTCTGA	84132
rs761025787	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6079008	GTTACTAAGGGTTTT[C/T]TGTTTGTAACAATTT	84132
rs761046718	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6127201	GTACTGTCAAGTTTT[A/G]AGGATATGTGGTTTC	84132
rs761049208	in-del	-/TT			intron-variant	USP42	GRCh38.p7	7:6102111	GTAGTCTCCTAAGAT[-/TT]TTTTTTTTTTTTTTT	84132
rs761063985	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103995	AGGCTAAGACAGGAA[C/T]ATCGCTTGAGCCCGG	84132
rs761074736	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077807	TTCTCCTGCCTCAGC[C/T]AACCAAGTTGCTGGG	84132
rs761078805	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094322	GGGACTACAGGCATG[C/T]ACCAGCACCTGGCTA	84132
rs761160266	snp	A/G/T	6.81122e-05	0.00583542	missense	USP42	GRCh38.p7	7:6150275	CTCAGAAAATCCCTT[A/G/T]GCTAAGGCAAACGGT	84132
rs761169257	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120373	TCAGCCTCCCAGGTA[A/G]CTGGGATTACAGGCA	84132
rs761169802	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104560	CTTCTGGAAACGCAT[C/G]TGGGGTCAAGCGCAG	84132
rs761190044	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6127610	GTGTGTCTGTCTCCA[C/G]GTTTCTGTTCTGTTG	84132
rs761197353	snp	A/C	6.43894e-05	0.00567367	missense	USP42	GRCh38.p7	7:6135945	TTTGTCATCAATGAG[A/C]TGCGGCGTAAGTATT	84132
rs761234740	snp	A/C	1.66197e-05	0.00288263	synonymous-codon	USP42	GRCh38.p7	7:6149930	AGTTTCTAGTAAAGT[A/C]ACAAAACCGATCCCC	84132
rs761239260	snp	A/C	0.000257522	0.0113444	missense	USP42	GRCh38.p7	7:6155134	GAGCCTAAAGCAAAG[A/C]AGCACAAAAAATCAA	84132
rs761241918	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6082213	GGCTCACTGCAAGCT[C/G]GGCCTCCCGGGTTCA	84132
rs761265224	snp	A/G	0.000106033	0.00728048	synonymous-codon	USP42	GRCh38.p7	7:6154038	CTTAACAGGCGATGC[A/G]AGCCCGTTGTCCCAG	84132
rs761265810	snp	A/G	3.31494e-05	0.00407107	intron-variant	USP42	GRCh38.p7	7:6150509	CGGATGAAATGAGGT[A/G]ACGTAAGAGTACATC	84132
rs761274857	snp	A/G	4.25269e-05	0.00461104	intron-variant	USP42	GRCh38.p7	7:6139080	AGCCTTGTCTTTACC[A/G]AAATTTTACAGGTAT	84132
rs761283886	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6157681	TATACGTTACTCTCC[C/G]GAATCCTTAAACCTG	84132
rs761284840	snp	A/C/G			intron-variant	USP42	GRCh38.p7	7:6099005	ACTCCTTCCTTATTA[A/C/G]AGTCCTGACTTTGGT	84132
rs761297074	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6111992	ATAATAACTTGTTAA[C/T]CAGTAGTTATTCTAG	84132
rs761298974	snp	C/G/T			intron-variant	USP42	GRCh38.p7	7:6106339	AGCGTAACAGTTTCT[C/G/T]TTTAAACGTGCTAAT	84132
rs761324153	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6149048	ACGCCTGCGCCTCCA[C/T]GGGGGTGCAGCAGCC	84132
rs761344277	snp	A/G	3.4024e-05	0.00412442	intron-variant	USP42	GRCh38.p7	7:6140896	TTGCTCATCTTTTGC[A/G]TTTTATTTTTATTTC	84132
rs761443806	snp	C/T			synonymous-codon	USP42	GRCh38.p7	7:6154473	GAGCAGGAGCAAGAC[C/T]GAGGGCCACCGTCAC	84132
rs761445415	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6089971	ACCTCACTGCACTCC[A/C]GCCTGGGCGACAGAG	84132
rs761512501	snp	C/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115261	TTTGACCAGGTGTTA[C/T]TATTTATTTAGCTTC	84132
rs761518776	snp	A/T	1.76677e-05	0.00297213	intron-variant	USP42	GRCh38.p7	7:6147729	TAAGTATCGCTCTCC[A/T]TGTTTCCAGGTCCCA	84132
rs761518936	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6149073	GCAGCCATGGGGGAA[C/T]CTGCAGCGAGTCTCA	84132
rs761523020	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6152764	AAGCTCTGCGGGAAT[A/C]AAAGGACAAAGTTAA	84132
rs761554150	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6096406	CATTGCATGGAGAGG[A/C]GGGATCCCAATGGTG	84132
rs761560041	snp	C/T	5.40906e-05	0.00520023	intron-variant	USP42	GRCh38.p7	7:6147689	TGTAAATGAATCTCT[C/T]CTAAGGAGGTGTCCT	84132
rs761583358	snp	C/T	3.31225e-05	0.00406941	intron-variant	USP42	GRCh38.p7	7:6140118	CATGTCACTGTTCAA[C/T]GTTTTTCAGATTAGA	84132
rs761607977	snp	G/T			downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161395	GGAGTGGGGAAAACT[G/T]TATTTAATACAGTTT	84132
rs761655731	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6097094	TATGTTTAGTAGAGA[C/T]GGGCTGCTATCATCC	84132
rs761656048	snp	C/G	4.87555e-05	0.00493714	intron-variant	USP42	GRCh38.p7	7:6144073	TATACTTTTGTTTCT[C/G]TTTGTTTCAAGGTGT	84132
rs761661348	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6078797	GCTTTCTTCTTTACT[A/T]CTCCAAATAGGGTGA	84132
rs761674708	snp	C/T	1.73788e-05	0.00294772	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116811	CCATAATTCATTCCC[C/T]ACAGACAGCTTTCCT	84132
rs761683002	snp	C/G/T	9.27917e-05	0.0068109	synonymous-codon	USP42	GRCh38.p7	7:6150020	GCTGGTGCCCTATGG[C/G/T]GCCGAGTCCTCTGAG	84132
rs761713222	snp	C/T	5.86711e-05	0.00541591	synonymous-codon	USP42	GRCh38.p7	7:6150098	TACGATTGTGAGCTC[C/T]CACTCTCCCGGCCAA	84132
rs761731666	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6150757	CTCCTGCGTGGCCAC[-/CT]CTCTCTGGTTAGCGG	84132
rs761733042	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6148196	TACAAGTATCAGCCG[G/T]GTATGGTGGTGTGTG	84132
rs761738161	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6121858	TAGAGACGAGGTCTC[A/G]CTATGTTGCCCAGGG	84132
rs761767842	snp	A/G/T	0.000140521	0.00838116	missense	USP42	GRCh38.p7	7:6153940	TGGGAGGCCATGGCC[A/G/T]TCGCCCCCGAGGAGC	84132
rs761776184	snp	A/T	5.21426e-05	0.00510574	intron-variant	USP42	GRCh38.p7	7:6116748	CTAGGGGTGTTTGTT[A/T]TGCCAGAATTAACGT	84132
rs761795912	snp	A/G	1.67908e-05	0.00289743	missense	USP42	GRCh38.p7	7:6156924	CTGTCGCCCAGTTCC[A/G]GAGAGCCCAGGGTGG	84132
rs761812317	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6123339	ACCAGCCTGAGCTAC[A/G]TAGTGAGACCCTCTC	84132
rs761815434	snp	C/T			utr-variant-5-prime	USP42	GRCh38.p7	7:6084571	GGCACTCCACATCGC[C/T]GCCCGCATCACCACG	84132
rs761824292	in-del	-/TGTT	2.50944e-05	0.00354211	intron-variant	USP42	GRCh38.p7	7:6144072	TTATACTTTTGTTTC[-/TGTT]TGTTTCAAGGTGTAA	84132
rs761824894	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6118696	AAGTTTATTTTTTTG[C/T]ATATGGATGTTCGGT	84132
rs761842857	in-del	-/C	1.738e-05	0.00294783	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116877	AAAACCCAGCACTAG[-/C]CACCTGGACAGCAAG	84132
rs761845592	snp	C/T	3.7691e-05	0.00434098	missense	USP42	GRCh38.p7	7:6154873	GGCTGCGAGCCGGCC[C/T]GGGAGAGGGAGCGGC	84132
rs761867418	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6134432	GGGATTTTTGTATTT[C/G]TTTAAAAAATATTTT	84132
rs761880903	snp	C/G/T	6.70425e-05	0.00578942	missense	USP42	GRCh38.p7	7:6150202	ACAGCGACAGTGACC[C/G/T]GAAAGAAAACGGCCT	84132
rs761949691	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6117975	TATATCCTCGATATA[A/T]GTCTTTTATTATGTA	84132
rs761972671	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151098	TAAACATAGAAAAGG[A/G]ACAGTAAAAATATGG	84132
rs762001293	snp	A/G	1.66518e-05	0.00288542	missense	USP42	GRCh38.p7	7:6147884	CAGCTTCCCTCTCAC[A/G]TGATAAAGGTAACAG	84132
rs762011280	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6157535	CTGAGTAGCCGGGAC[-/T]TACAGGCGCCCGCCA	84132
rs762033022	snp	C/T			utr-variant-5-prime	USP42	GRCh38.p7	7:6088882	AGGGGACGGCGGGAA[C/T]CAAGATTGGAAGGAA	84132
rs762046521	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6135419	TTGGGAGGCCAAGGT[A/G]GGTGGATTGCCTGAG	84132
rs762051797	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6098833	TTACAGGCATGAGCC[A/G]CCATGCCCTGCCAAG	84132
rs762067432	snp	C/G	1.76811e-05	0.00297326	missense	USP42	GRCh38.p7	7:6154033	GGGAGCTTAACAGGC[C/G]ATGCGAGCCCGTTGT	84132
rs762113758	snp	A/G	3.31279e-05	0.00406975	missense	USP42	GRCh38.p7	7:6145570	ATGTCTCAACCCAAC[A/G]GAGAGCCAATTGTCT	84132
rs762114615	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131046	AGTTTTGCCTCCTGG[A/G]GTGCACAGGCAGGTG	84132
rs762154876	snp	C/G	3.84261e-05	0.0043831	missense	USP42	GRCh38.p7	7:6154546	CGCCACGCCCCGGAG[C/G]ACCACCCCGGCCACG	84132
rs762182643	snp	C/T	2.91032e-05	0.00381454	intron-variant	USP42	GRCh38.p7	7:6135810	TATGGTTGTATTTTG[C/T]TAATTTGGAGGATTA	84132
rs762208080	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6125684	TCTGTTTACCTACTT[A/G]TTTACTGTTTTCACT	84132
rs762210725	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6100815	GGGATTATAGGCGCG[C/T]GCTACCACACTCAGC	84132
rs762224837	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6158802	GGGCTCATTCTGAGT[G/T]TGGTGCAGGCTCCCA	84132
rs762249719	snp	A/G	0.000153245	0.00875209	missense	USP42	GRCh38.p7	7:6154484	AGACTGAGGGCCACC[A/G]TCACCGGCGGCGCCG	84132
rs762309787	snp	C/T	1.66139e-05	0.00288213	intron-variant	USP42	GRCh38.p7	7:6145478	GTGGAATGATCTGTG[C/T]CCTCGGAAATGTTTC	84132
rs762314250	snp	A/G	2.10675e-05	0.0032455	intron-variant	USP42	GRCh38.p7	7:6140010	ATCCTTTTATTTTCC[A/G]TGGCTGTCCTGTTTG	84132
rs762322556	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120495	TGATCTGCCCGACTC[A/G]GCCTCCCAAAGTGCT	84132
rs762331236	snp	A/C	1.78963e-05	0.00299129	synonymous-codon	USP42	GRCh38.p7	7:6153993	CATCGTGGGGGACAC[A/C]GCACCCCCTGACCTG	84132
rs762343298	snp	C/T	5.77001e-05	0.00537091	synonymous-codon	USP42	GRCh38.p7	7:6154689	CGAGCGTGGCTGGGG[C/T]CGGGAGAAGTTCTAC	84132
rs762385180	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6085182	TGGAGTGCAGTGACA[A/T]GATCTTCACTTACTG	84132
rs762397898	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130069	TGGCTCACTGCAGCT[C/T]CCACCTCCTGGGCTC	84132
rs762402765	snp	A/G	2.07475e-05	0.00322077	intron-variant	USP42	GRCh38.p7	7:6111406	GAGAGAATTACCGCC[A/G]GAAACTCCTGTGTAA	84132
rs762441877	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6101516	CTGGATTACACTCTG[A/T]TCTGGAGGAGAACAA	84132
rs762450809	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6139989	TCTTGGGCTGCCACA[C/T]GTGCCATCCTTTTAT	84132
rs762457064	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6128776	TTTGAATACTTGAAA[A/G]TGTTTTTCAAAATTA	84132
rs762611570	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6127775	TCGTTACAAATTATA[A/G]AATAATCTATATAAA	84132
rs762619369	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6150742	ACCATGCTATTTCTC[C/T]TCCTGCGTGGCCACC	84132
rs762634301	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6121067	TTAAGATTTTATAGA[C/T]GCAACTATGTGATAC	84132
rs762672598	snp	C/T	3.65163e-05	0.0042728	intron-variant	USP42	GRCh38.p7	7:6115560	TGTAGTATTGTAGTG[C/T]GCTAACCTACTTTCA	84132
rs762675651	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6148315	GCACTCCAGCCTGGG[C/T]AACAGAGTGAGACCC	84132
rs762680263	snp	A/G	8.94975e-05	0.00668885	missense	USP42	GRCh38.p7	7:6150003	AAGCTGAACTCCAGC[A/G]TGCTGGTGCCCTATG	84132
rs762696904	snp	C/T	5.63428e-05	0.00530737	intron-variant	USP42	GRCh38.p7	7:6146289	GATTTTCTGGTATGT[C/T]ATTTCTTCTTGTCTT	84132
rs762710250	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6084869	AACTACAGGTGTGTG[C/T]CATCATGCCTGGCTA	84132
rs762724482	in-del	-/A			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103740	ACCCCCGTCTCTACA[-/A]AAAAAAAAAAAAAAA	84132
rs762736924	snp	A/G/T	0.000125522	0.00792136	synonymous-codon	USP42	GRCh38.p7	7:6154278	GCTGGACATGGCCCC[A/G/T]GCCGGTCACCCGGAA	84132
rs762741874	snp	A/G	7.15538e-05	0.00598095	missense	USP42	GRCh38.p7	7:6153994	ATCGTGGGGGACACA[A/G]CACCCCCTGACCTGT	84132
rs762778458	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6115896	TCGAGCCCAAGAGTT[A/G]GAGACCAACCTGGAC	84132
rs762789239	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098473	TCCTCCCTTAGCAGG[C/T]GTGATGGTATCTGAT	84132
rs762792064	snp	C/T	3.51543e-05	0.00419237	intron-variant	USP42	GRCh38.p7	7:6149552	ACCATGTTTCTGGAG[C/T]TCTGACCAGGTGCGC	84132
rs762809109	snp	C/T	1.66067e-05	0.00288151	synonymous-codon	USP42	GRCh38.p7	7:6143009	AAACTCGTACAAGTG[C/T]AGCAAGTACGTTGGG	84132
rs762817413	snp	C/G	1.77234e-05	0.00297681	missense	USP42	GRCh38.p7	7:6153876	CAGCAGCACCAAGAA[C/G]GCTCCGCCGCCCCGC	84132
rs762826874	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6157701	CCTTAAACCTGTAGC[A/T]TTCTGAGTGCACCCT	84132
rs762845129	snp	C/T	0.000122152	0.00781417	synonymous-codon	USP42	GRCh38.p7	7:6153900	GCCCCGCGATCCCGG[C/T]ACCCCCGCTACCAAA	84132
rs762871519	snp	A/G	1.6782e-05	0.00289668	intron-variant	USP42	GRCh38.p7	7:6142909	GTGCGGTGATGTGGT[A/G]TTTGTGCCTCTTCTC	84132
rs762902006	snp	C/G	1.65614e-05	0.00287757	missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115416	ATAGAGTTGGAGCTG[C/G]GCTCCAGAATTTGGG	84132
rs762905530	in-del	-/TCTT	1.66247e-05	0.00288307	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115301	AGCTTGGTTTCTGAC[-/TCTT]TCTTGTTTATTTTTC	84132
rs762970310	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6089212	ACCACGCCTGGCTAA[-/T]TTTTTTTTTTTTTGT	84132
rs762972015	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104718	CCCTCTGCCGGCCCG[A/C]CCGGCGCTCTGGTGA	84132
rs762997517	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6101572	AGCCAAGGCCCCAGC[C/T]GTTTGTAGGCAGGGA	84132
rs763013666	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6116732	GAATCTCACCACCTA[C/T]CTAGGGGTGTTTGTT	84132
rs763015434	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6116569	AAAAAAAATCCTTGG[-/T]TTCTTTTTGAATAGT	84132
rs763015831	snp	G/T	4.8765e-05	0.00493762	intron-variant	USP42	GRCh38.p7	7:6157098	GATAGAAACTATTTC[G/T]TAATACATTTTCTTT	84132
rs763020968	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6109376	GGCCACTCCTGAAAG[G/T]TGTTCTTTCTTCCTT	84132
rs763051815	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6132118	TTTGTAGAGACAGGA[C/T]TTTGGCCATTTTGGC	84132
rs763062447	snp	A/G	1.82784e-05	0.00302305	missense	USP42	GRCh38.p7	7:6135910	CACTCAGTAATCCTG[A/G]GGACGTTATTAAACC	84132
rs763081290	snp	G/T	3.38782e-05	0.00411557	intron-variant	USP42	GRCh38.p7	7:6144246	CGAGCCTTTCGAAGC[G/T]TAACGTGTCTGTAGC	84132
rs763083809	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6147190	CTCAGGCCAAGTTGA[-/G]GGGTAGGATTTTGTT	84132
rs763106672	snp	G/T	3.59499e-05	0.00423953	missense	USP42	GRCh38.p7	7:6154759	GACAGGTACGCCCTG[G/T]ACGCTGCCCGGGACT	84132
rs763108994	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080604	TTGCCAGGAGCCTGA[C/G]GCAGGACAATCGCTT	84132
rs763112383	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6142703	GCCTGGGGGAATATA[C/G]TGAGACCCCTGTCTC	84132
rs763119681	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077413	CTTTCATCTTACTCT[C/T]TCCCTCTTTCATCTG	84132
rs763147467	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6119463	GCAGCAGAGTGAGAT[C/T]TTACGTCAACCAAAA	84132
rs763164165	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6079259	GTCAGGAGATCGAGA[C/T]CACCCTGGCTAACAC	84132
rs763197616	snp	A/G	0.000114541	0.00756686	missense	USP42	GRCh38.p7	7:6154459	GAGCCCGCCAGAGAG[A/G]GCAGGAGCAAGACTG	84132
rs763217991	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6102936	GATGGAATTGTTGAG[C/T]GAAGAAAGGCTGACT	84132
rs763237987	snp	G/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103431	ATCCCAGGTACTTAG[G/T]AGGCTGAGGCAGGAG	84132
rs763262511	snp	C/G	5.37986e-05	0.00518618	missense	USP42	GRCh38.p7	7:6153990	GGACATCGTGGGGGA[C/G]ACAGCACCCCCTGAC	84132
rs763275116	snp	A/C	1.65625e-05	0.00287766	missense	USP42	GRCh38.p7	7:6149780	AATCAGTATTCACAA[A/C]AAGTTGCCTGTTCGC	84132
rs763290571	snp	C/T	1.65627e-05	0.00287769	intron-variant	USP42	GRCh38.p7	7:6135795	GCCTTGATGTGTGTA[C/T]ATGGTTGTATTTTGC	84132
rs763336203	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6159118	TCCCCCTCTACCCTG[A/G]ACTTCGGCCCCTTGT	84132
rs763337470	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6118768	TAAATTGTCTTTGCA[C/T]CTTTATCAAAAATCA	84132
rs763347135	in-del	-/AT			intron-variant	USP42	GRCh38.p7	7:6082940	TATATATAGATACAT[-/AT]ATATATATATATTTA	84132
rs763354087	in-del	-/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6078734	CCAACTGTCTGATGG[-/T]TAAGTCCCAGATACG	84132
rs763365997	snp	A/G	1.85012e-05	0.00304143	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111172	TGAATCTTCAGACCC[A/G]TCAGCCTATCAGAAT	84132
rs763367440	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6089062	TTATATTTATCTTTT[C/T]GAAATGGAGTTTCAC	84132
rs763374963	snp	A/C	8.2085e-05	0.00640591	missense	USP42	GRCh38.p7	7:6155120	AGGATCCTCTAGAAG[A/C]GCCTAAAGCAAAGAA	84132
rs763395735	snp	G/T	3.31296e-05	0.00406985	missense	USP42	GRCh38.p7	7:6150454	CCAGAAGACAAAATC[G/T]TAGAGACCTTCAGGC	84132
rs763412181	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6136952	CTTAATTACAGTCTT[A/G]AAAGAATATATACTC	84132
rs763418622	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6101721	AGGGGGAGGTGTAAC[C/T]CCCCATCCCCTCCAA	84132
rs763424836	snp	C/T	5.58301e-05	0.00528317	synonymous-codon	USP42	GRCh38.p7	7:6144155	GTTCTTACACTTTCT[C/T]TGAAACGTTTTGCAA	84132
rs763471439	snp	A/G	0.000348008	0.0131865	synonymous-codon	USP42	GRCh38.p7	7:6154395	CGGCAGCCTCAGAAA[A/G]GTGGACCGAGGCCAC	84132
rs763497389	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159685	CAGACCTAGACCCTC[C/T]ACCTCATCACGTTTG	84132
rs763503884	snp	A/G	1.69752e-05	0.0029133	missense	USP42	GRCh38.p7	7:6155045	CCCGGAAACGGAGAC[A/G]CGACAGTGTGGAGAA	84132
rs763514616	snp	C/G	1.6569e-05	0.00287824	intron-variant	USP42	GRCh38.p7	7:6140096	AGTTTTTGCAAAGCT[C/G]TTCTCTCATGTCACT	84132
rs763547672	snp	C/T	6.62405e-05	0.00575464	synonymous-codon	USP42	GRCh38.p7	7:6149681	CAACAGGGCTAGTCC[C/T]GTTAATGCTTCAGCT	84132
rs763584631	snp	A/G	1.68949e-05	0.0029064	intron-variant	USP42	GRCh38.p7	7:6150372	TTCAGGAGGCATGGA[A/G]CTGGCGACTGAAGCT	84132
rs763596906	snp	C/G	1.65647e-05	0.00287786	missense	USP42	GRCh38.p7	7:6150457	GAAGACAAAATCTTA[C/G]AGACCTTCAGGCTTA	84132
rs763616619	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6151923	TGATCTTATGGACCG[A/C]CATCATATGTGGTCT	84132
rs763621598	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6102052	GACAGGGTGACATTC[C/T]ACCTTAATTCACAAA	84132
rs763639489	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6122162	TCTTAAGGTGGAGTC[-/T]TTAGGTCATTTGATT	84132
rs763643443	snp	C/G/T	3.63889e-05	0.00426537	missense	USP42	GRCh38.p7	7:6154132	TTGAGTCCGGCTCCG[C/G/T]CTGCGCGGTCGGAGG	84132
rs763659813	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159215	TCTAACATCAGGCTG[C/T]GTGTGGGTTGGATGG	84132
rs763666229	snp	A/G	1.72826e-05	0.00293956	intron-variant	USP42	GRCh38.p7	7:6149571	GACCAGGTGCGCTCT[A/G]CTTACTTCCAGAATC	84132
rs763671686	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159899	CTCCCTCGTCCGTCC[C/T]GTCCCCTGTGCTGCT	84132
rs763685659	snp	G/T	4.16415e-05	0.00456279	intron-variant	USP42	GRCh38.p7	7:6140016	TTATTTTCCATGGCT[G/T]TCCTGTTTGAATTCT	84132
rs763700898	snp	C/T	1.86308e-05	0.00305206	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111179	TCAGACCCATCAGCC[C/T]ATCAGAATCAGCCTG	84132
rs763720941	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138152	GAGTGTTGGCAGTTT[C/T]ATGTGATTTAAGCTA	84132
rs763773392	snp	A/G	2.73856e-05	0.00370028	missense	USP42	GRCh38.p7	7:6139110	TAGCTAGGCACTTCC[A/G]TTTTGGAAACCAAGA	84132
rs763780817	snp	A/G	1.78669e-05	0.00298883	synonymous-codon	USP42	GRCh38.p7	7:6154101	GGACTCGGCGTTGGC[A/G]GAAGCCCCGGAAGGG	84132
rs763783008	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103162	AGGCCTCGAGGTGGA[C/G]ACAGCCAATAAATGA	84132
rs763798050	snp	C/T	0.000239837	0.0109481	intron-variant	USP42	GRCh38.p7	7:6146294	TCTGGTATGTCATTT[C/T]TTCTTGTCTTATCAA	84132
rs763808328	snp	A/G	5.38508e-05	0.00518869	synonymous-codon	USP42	GRCh38.p7	7:6150005	GCTGAACTCCAGCGT[A/G]CTGGTGCCCTATGGC	84132
rs763813423	snp	A/C/G	0.000177438	0.0094177	missense	USP42	GRCh38.p7	7:6154633	TCCCGACACCGGAGC[A/C/G]GGGTGGAGCTGGACT	84132
rs763843037	snp	C/G	2.89842e-05	0.00380674	missense	USP42	GRCh38.p7	7:6154690	GAGCGTGGCTGGGGC[C/G]GGGAGAAGTTCTACC	84132
rs763874758	snp	A/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113626	TTTTTTGTTTTTGTT[A/T]TTGTTTTTTTTTTGA	84132
rs763879767	snp	C/T	3.47397e-05	0.00416757	synonymous-codon	USP42	GRCh38.p7	7:6154587	CAGCCCTGGCGAGCG[C/T]CGCTCTCTGGGCAGG	84132
rs763891359	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6098536	AGGAACAGAAAGAAT[C/G]CATTGTTTTCTTGTT	84132
rs763896390	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126772	TTGTGAGTGGAGCTG[C/T]GGTAAACATCCAGGT	84132
rs763920483	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130434	GCCTCTGACCCTCAC[C/T]GGGGGCTGGGGAGGC	84132
rs763944896	snp	C/G/T	0.000200754	0.0100169	missense	USP42	GRCh38.p7	7:6149946	ACAAAACCGATCCCC[C/G/T]GCAGTGAATCCTGCT	84132
rs763947743	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6152912	GAGAAAGGGAGTCGA[A/G]AGGAAAGGAGGAGGC	84132
rs763951872	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130900	CTTCGTTGAGGTTTC[C/T]GTGGGAAAAGCAGGG	84132
rs763953317	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095672	AGACTCCGTCTAAAA[A/G]ACAAAAAAAATGGCC	84132
rs763981566	snp	C/G	3.31225e-05	0.00406941	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115417	TAGAGTTGGAGCTGG[C/G]CTCCAGAATTTGGGC	84132
rs763999195	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6122039	GCTCTTGGTTTCATT[C/G]TTACAGTTTTCTGTT	84132
rs764011521	snp	C/T	5.54155e-05	0.00526352	missense	USP42	GRCh38.p7	7:6154766	ACGCCCTGTACGCTG[C/T]CCGGGACTGGAAGCC	84132
rs764022677	snp	A/G	0.00011627	0.00762376	missense	USP42	GRCh38.p7	7:6143011	ACTCGTACAAGTGCA[A/G]CAAGTACGTTGGGTG	84132
rs764026059	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6156047	CACCTGGCCTGTTTT[C/T]GTATTTTTAAAAAGC	84132
rs764034577	snp	A/G	1.82894e-05	0.00302396	intron-variant	USP42	GRCh38.p7	7:6115561	GTAGTATTGTAGTGC[A/G]CTAACCTACTTTCAT	84132
rs764093779	snp	A/C/T	6.63134e-05	0.00575786	intron-variant	USP42	GRCh38.p7	7:6159505	TATGGTAAGCTGTTT[A/C/T]CCTGTCTGTTTCCTC	84132
rs764105545	snp	C/T	1.86687e-05	0.00305516	synonymous-codon	USP42	GRCh38.p7	7:6154194	CAGCGGGGACCACGC[C/T]CGGGACGCTCAGGAC	84132
rs764107127	in-del	-/C	5.07868e-05	0.00503893	intron-variant	USP42	GRCh38.p7	7:6115533	AAACATGTAAGTGTT[-/C]CGTGTTGTGTTTGTA	84132
rs764138389	snp	G/T	0.000242542	0.0110096	missense	USP42	GRCh38.p7	7:6153877	AGCAGCACCAAGAAG[G/T]CTCCGCCGCCCCGCG	84132
rs764146440	snp	A/C	1.7112e-05	0.00292501	missense	USP42	GRCh38.p7	7:6156840	AGAAAAAGAAGAGAC[A/C]TTCAAGAAAATCAGA	84132
rs764173817	snp	A/G	1.65721e-05	0.0028785	missense	USP42	GRCh38.p7	7:6147815	TCTCCCCGCCCCGTC[A/G]TCAGTCAGCGGGTTG	84132
rs764192420	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6117347	TCAGCATAATCCTGT[C/T]AACATTATTCCATTT	84132
rs764239924	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6141669	GTTCAAGCATTTCCC[-/CT]GTCTCAGCCTCCCTA	84132
rs764254513	snp	A/G	0.000557776	0.0166906	missense	USP42	GRCh38.p7	7:6154870	AGGGGCTGCGAGCCG[A/G]CCCGGGAGAGGGAGC	84132
rs764268159	snp	G/T	1.90976e-05	0.00309006	missense	USP42	GRCh38.p7	7:6157041	ACAGGTGTCGTCTCT[G/T]TGAGTATGGCCAGGG	84132
rs764275767	snp	A/G	1.79123e-05	0.00299263	missense	USP42	GRCh38.p7	7:6153991	GACATCGTGGGGGAC[A/G]CAGCACCCCCTGACC	84132
rs764334859	snp	A/C	1.91243e-05	0.00309221	missense	USP42	GRCh38.p7	7:6144170	CTGAAACGTTTTGCA[A/C]ATTTTACCGGTGGAA	84132
rs764338630	snp	C/G	6.04284e-05	0.00549641	intron-variant	USP42	GRCh38.p7	7:6135798	TTGATGTGTGTATAT[C/G]GTTGTATTTTGCTAA	84132
rs764349842	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6117823	CCTCTTTTCTTTTTT[A/G]TTTTGTTTTTGTTTT	84132
rs764364377	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6141513	AATTTTCATTTAATA[C/T]CTTAATAAAACTAGA	84132
rs764364605	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6148694	CCTCATCTGAGCTGT[-/G]GGCATCTTCACAGCT	84132
rs764375217	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6107656	TCAGGTGATCTGCCC[A/G]CCTCGTCCTCCCAAA	84132
rs764381276	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151062	CCGTAGGCAGCTGTA[A/G]TACAGTGGTATTTGT	84132
rs764409118	snp	C/G	6.62471e-05	0.00575492	missense	USP42	GRCh38.p7	7:6149783	CAGTATTCACAACAA[C/G]TTGCCTGTTCGCCAG	84132
rs764417468	in-del	-/TA			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080101	GGTGGCGGACGCCTG[-/TA]GTCCCAGCTACTCGG	84132
rs764457706	snp	G/T	1.65605e-05	0.0028775	missense	USP42	GRCh38.p7	7:6149710	CTTCTGTCCAAAACT[G/T]GTCAGTTAATAGGTC	84132
rs764470038	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6158549	CGGTCCTTAGAGTGT[A/G]TGAGAGAGAGCTGGG	84132
rs764499268	snp	C/T	0.000174795	0.00934702	synonymous-codon	USP42	GRCh38.p7	7:6154401	CCTCAGAAAGGTGGA[C/T]CGAGGCCACTACCGC	84132
rs764503806	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081196	GGTGGGAGTGTCTTC[C/T]CCCGACACCCCGTAT	84132
rs764524642	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104261	CTAATTTTTTGTATC[C/T]TTAGTAGAGACAGGG	84132
rs764555152	snp	A/G	2.03341e-05	0.00318852	synonymous-codon	USP42	GRCh38.p7	7:6153951	GGCCGTCGCCCCCGA[A/G]GAGCCTCCGCCCAGC	84132
rs764555915	in-del	-/TTATTTAT			intron-variant	USP42	GRCh38.p7	7:6083228	CCGCACCCAGCTTAT[-/TTATTTAT]TTATTTATTTATTTA	84132
rs764575757	snp	A/G	1.66175e-05	0.00288244	intron-variant	USP42	GRCh38.p7	7:6145467	TACCTGAATATGTGG[A/G]ATGATCTGTGCCCTC	84132
rs764585849	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6079449	GGCGACAGAGCCAGA[-/CT]CTGTCTCAAAAATAA	84132
rs764627084	in-del	-/GCTGCAGT			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104127	CGCCCAGGCTGGAGG[-/GCTGCAGT]GCTGCAGTGCAGAGG	84132
rs764657101	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6149478	AACTTGTTAGTCCTG[A/G]AAAAAAAAAAAAGCA	84132
rs764668370	snp	C/T	4.15291e-05	0.00455662	missense	USP42	GRCh38.p7	7:6154624	CACCACCACTCCCGA[C/T]ACCGGAGCGGGGTGG	84132
rs764670476	snp	A/G	1.76661e-05	0.00297199	synonymous-codon	USP42	GRCh38.p7	7:6154044	AGGCGATGCGAGCCC[A/G]TTGTCCCAGGACGCA	84132
rs764678574	snp	A/G			utr-variant-5-prime	USP42	GRCh38.p7	7:6093051	TGTGACTGAGTCTCC[A/G]TGTGGGCTGCTGGGA	84132
rs764693461	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6100793	TGCCTCAGCCTCCTG[A/G]GTAGCTGGGATTATA	84132
rs764729359	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6091899	CAATCGGCATTTCTT[C/T]CTGAAATGCTGGCTG	84132
rs764729755	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6134257	GAATATATTTGTAAT[A/G]TCCTTTTTAAAGTTA	84132
rs764730764	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120429	TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACAGT	84132
rs764738776	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6082240	TTCACGCCATTCTCC[C/T]GCCTCAGCCTCCCGA	84132
rs764738787	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6112004	TAACCAGTAGTTATT[C/T]TAGTTTCCTAAGTAG	84132
rs764749264	snp	A/G	3.31488e-05	0.00407103	missense	USP42	GRCh38.p7	7:6145588	GAGCCAATTGTCTAC[A/G]TCTTGTATGCAGTGC	84132
rs764751875	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6145240	GGAGGCTGAGGCAGG[A/G]CAATCACTTGAACCC	84132
rs764757439	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6144334	TTGGGCTTCATTGTC[G/T]GTTTTGTTGGTACCC	84132
rs764760055	snp	C/G	1.78169e-05	0.00298465	missense	USP42	GRCh38.p7	7:6154098	GCGGGACTCGGCGTT[C/G]GCGGAAGCCCCGGAA	84132
rs764761303	snp	C/G	1.80357e-05	0.00300292	missense	USP42	GRCh38.p7	7:6155121	GGATCCTCTAGAAGA[C/G]CCTAAAGCAAAGAAG	84132
rs764767085	snp	A/G	8.31152e-05	0.00644598	missense	USP42	GRCh38.p7	7:6154345	GACGCCGCGGCGCCG[A/G]AAGCCCCAGGCCCTT	84132
rs764772978	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6127622	CCAGGTTTCTGTTCT[A/G]TTGTGATGATGTATG	84132
rs764773106	snp	C/T	5.89675e-05	0.00542957	intron-variant	USP42	GRCh38.p7	7:6146101	CTTGACTATGTTCCA[C/T]GTTTAATTAAATCTA	84132
rs764773668	snp	A/C	1.74482e-05	0.00295361	missense	USP42	GRCh38.p7	7:6156830	AAAAAGAAGAAGAAA[A/C]AGAAGAGACATTCAA	84132
rs764835630	snp	A/G	1.71264e-05	0.00292624	missense	USP42	GRCh38.p7	7:6150285	CCCTTTGCTAAGGCA[A/G]ACGGTCTTCCTGGAA	84132
rs764842115	snp	A/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077808	TCTCCTGCCTCAGCC[A/T]ACCAAGTTGCTGGGA	84132
rs764850182	snp	C/T	3.69843e-05	0.00430009	intron-variant	USP42	GRCh38.p7	7:6139089	TTTACCGAAATTTTA[C/T]AGGTATAGCTAGGCA	84132
rs764876089	snp	A/C	0.000215301	0.0103732	missense	USP42	GRCh38.p7	7:6149838	AGTAATTCTTTGGAG[A/C]ACCCTACCAAGCCCG	84132
rs764899064	in-del	-/A			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115001	GCCCTATATATATAT[-/A]TTTTTTAAGCAGTTG	84132
rs764902406	snp	C/T			utr-variant-5-prime	USP42	GRCh38.p7	7:6084590	CGCATCACCACGCTG[C/T]GGCATCTGCTGTTGC	84132
rs764907801	in-del	-/AAAAAAAAGAAG	1.93727e-05	0.00311223	cds-indel	USP42	GRCh38.p7	7:6156812	GACCTCCACAGACAC[-/AAAAAAAAGAAG]AAGAAAAAGAAGAGA	84132
rs764927290	snp	A/C			missense	USP42	GRCh38.p7	7:6156980	CTGGAAGGCGTCGGA[A/C]CTTTCCGTGAGAAAA	84132
rs764934568	snp	C/G	0.000135805	0.00823918	missense	USP42	GRCh38.p7	7:6154577	GCGACAGGCTCAGCC[C/G]TGGCGAGCGCCGCTC	84132
rs764981022	snp	A/G	1.65605e-05	0.0028775	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115396	TCTTAAGTGGCAACA[A/G]ACTCATAGAGTTGGA	84132
rs765001844	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6119939	ACTCCTACGCTTAAG[C/T]GGTTCTCTTGCCTCA	84132
rs765002750	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6147525	CACAGTTTAAAGAAC[A/G]TCATTTACCCAGTTA	84132
rs765090820	snp	A/G			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161727	AGGAAAATTGGAGGG[A/G]TGTTTGCTGGACCCA	84132
rs765092639	snp	C/T	1.6571e-05	0.0028784	synonymous-codon	USP42	GRCh38.p7	7:6140973	TATCTTGATATAACA[C/T]TGGAGATAAAGGTAA	84132
rs765098412	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6134476	AAGACAGAGTTAATT[-/G]GGAATAGCTTGATCC	84132
rs765111328	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6138319	CAGGACTGAAATGTT[G/T]CTGTGCACCTGCAAA	84132
rs765114712	snp	A/C	0.000182498	0.0095507	synonymous-codon	USP42	GRCh38.p7	7:6153822	GCCTGGCAGCCCCGC[A/C]GCCGAATCCCTGGAG	84132
rs765116121	snp	A/C			missense	USP42	GRCh38.p7	7:6154525	CGGGAGCGCGACCGC[A/C]AGGACCGCCACGCCC	84132
rs765118419	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6156085	GTTGGTGATTGTCTT[C/G]AAAATGACGTATCCA	84132
rs765128993	snp	A/G	8.28205e-05	0.00643455	missense	USP42	GRCh38.p7	7:6149875	CTTCTACCATTACCA[A/G]TTCTGCAGTACAGTC	84132
rs765131139	snp	A/G	1.78966e-05	0.00299132	missense	USP42	GRCh38.p7	7:6153868	GCCGGCCTCAGCAGC[A/G]CCAAGAAGGCTCCGC	84132
rs765159602	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6132706	AGACGGAGTTTTGCT[C/G]TGTTGCCCAGGCTGG	84132
rs765164257	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6137372	ATTCATTCATCCATT[C/G]ATTTGAGATGGAGTC	84132
rs765216642	snp	A/G			missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6115454	TGTTTTGCCAATGCA[A/G]CACTGCAGTGTTTAA	84132
rs765250225	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6099034	GTGTTAGAGACTGAT[A/C]GTAGCTGAAAATTCA	84132
rs765261624	snp	C/T	2.29476e-05	0.00338722	missense	USP42	GRCh38.p7	7:6154229	CCCAGAGCTTGGGCG[C/T]ACCCGAGGCCGCAGA	84132
rs765290980	snp	C/T	1.9377e-05	0.00311258	synonymous-codon	USP42	GRCh38.p7	7:6150044	CTCTGAGGACTCTGA[C/T]GAGGAGTCAAAGGGG	84132
rs765392791	snp	C/T	3.47572e-05	0.00416862	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116824	CCCACAGACAGCTTT[C/T]CTATCACTTTTGCGC	84132
rs765419192	snp	A/T	1.70295e-05	0.00291796	missense	USP42	GRCh38.p7	7:6154384	AAGGAGAAAATCGGC[A/T]GCCTCAGAAAGGTGG	84132
rs765425503	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095826	GGGCTGCAGTGGTGT[A/G]GTCACATCTCACTGC	84132
rs765430175	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6079119	CAACATTGAATACAT[G/T]TATAAAATATTTCAA	84132
rs765430920	snp	C/G/T	0.000102044	0.00714235	missense	USP42	GRCh38.p7	7:6154705	CGGGAGAAGTTCTAC[C/G/T]CCGACAGGCCGCGCT	84132
rs765474640	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6085186	GTGCAGTGACATGAT[A/C]TTCACTTACTGCAAC	84132
rs765483540	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6101335	CCTTCCTGACACCTA[C/T]TGTTCCATGATCCTG	84132
rs765488783	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6125037	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCTCA	84132
rs765492500	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6096416	AGAGGAGGGATCCCA[A/G]TGGTGCAGATGCAGT	84132
rs765492705	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6139478	TATCAGCAGACGTCT[A/G]CAGATCTCAAACTAG	84132
rs765497645	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6122145	ATGTGCTCTGTTCCA[A/G]TGTCTTAAGGTGGAG	84132
rs765501731	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6132051	AATCCTCCCACCTCA[A/G]CTTCCTGAATAGCTG	84132
rs765511188	in-del	-/TTTTA			intron-variant	USP42	GRCh38.p7	7:6157380	CTTGGTTTGGTTTGG[-/TTTTA]TTTTATTTTATTTTA	84132
rs765517745	snp	C/T	1.82607e-05	0.00302159	synonymous-codon	USP42	GRCh38.p7	7:6144139	CCATAGATCCTCTAA[C/T]GTTCTTACACTTTCT	84132
rs765519327	snp	A/G/T	5.21375e-05	0.00510553	intron-variant	USP42	GRCh38.p7	7:6149566	GCTCTGACCAGGTGC[A/G/T]CTCTGCTTACTTCCA	84132
rs765533705	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6108533	GTCGCCAGGCTGGAG[C/T]GCAGTGGCGCGATCT	84132
rs765536616	in-del	-/TGTT	0.000439657	0.0148201	intron-variant	USP42	GRCh38.p7	7:6153732	CCACGCTAACGGGCG[-/TGTT]TGTTTGTTTGGGGGC	84132
rs765590370	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6101626	CTCCATTAATGTTGC[C/T]AGTTTGCTAGAGTAA	84132
rs765618307	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6151111	GGGACAGTAAAAATA[C/T]GGTATAAGAGGAAAA	84132
rs765622235	snp	G/T	9.27128e-05	0.00680792	intron-variant	USP42	GRCh38.p7	7:6139230	GCCATGTCTTCATTG[G/T]GGATCTCTGGTTGTA	84132
rs765625379	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6131193	AGAAAGATCTTTAGG[A/G]TGTCAAAACATCATA	84132
rs765628332	in-del	-/AAA			upstream-variant-2KB	USP42	GRCh38.p7	7:6078602	GCAAGACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA	84132
rs765629555	snp	C/G	1.69617e-05	0.00291214	synonymous-codon	USP42	GRCh38.p7	7:6155040	AAAGTCCCGGAAACG[C/G]AGACACGACAGTGTG	84132
rs765649608	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6087687	GAGATATTTTTCAGC[A/G]AGAGTGTGAATCTTC	84132
rs765656560	snp	A/G	0.000161303	0.00897918	missense	USP42	GRCh38.p7	7:6154336	AGGGTCGAGGACGCC[A/G]CGGCGCCGAAAGCCC	84132
rs765670169	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6159687	GACCTAGACCCTCCA[A/C]CTCATCACGTTTGCA	84132
rs765712996	snp	C/T	1.67441e-05	0.0028934	intron-variant	USP42	GRCh38.p7	7:6143052	TCTTGATGCCGGCTT[C/T]TCCAGTGGGGATGGC	84132
rs765749140	snp	A/G	1.83609e-05	0.00302987	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111168	CTTCTGAATCTTCAG[A/G]CCCATCAGCCTATCA	84132
rs765785263	snp	C/T	0.000144139	0.00848815	missense	USP42	GRCh38.p7	7:6150139	ATGAGGAGGCCACTC[C/T]GCACGAGCTTCAAGA	84132
rs765809107	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6089012	AGAGCCTGCACTGGG[G/T]TTTCTTTTCTATATT	84132
rs765819108	snp	A/T	0.000132806	0.00814772	missense	USP42	GRCh38.p7	7:6156808	CGCTGACCTCCACAG[A/T]CACAAAAAAAAGAAG	84132
rs765822394	in-del	-/T	1.7274e-05	0.00293883	intron-variant	USP42	GRCh38.p7	7:6149572	CCAGGTGCGCTCTGC[-/T]TTACTTCCAGAATCC	84132
rs765824448	snp	A/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077947	CCACCTCAGCCTCCC[A/T]AAGTGGGCGTGAGCC	84132
rs765838732	snp	A/G	1.80455e-05	0.00300373	missense	USP42	GRCh38.p7	7:6154565	ACCCCGGCCACGGCG[A/G]CAGGCTCAGCCCTGG	84132
rs765851370	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6127994	TGGTGTGATCATAGC[C/T]CACTGCATCCTCAAA	84132
rs765858844	snp	C/T	0.000170547	0.00923278	missense	USP42	GRCh38.p7	7:6154495	CACCGTCACCGGCGG[C/T]GCCGCACCTGCCCCC	84132
rs765874355	snp	C/T	1.658e-05	0.00287919	intron-variant	USP42	GRCh38.p7	7:6145497	CGGAAATGTTTCTCC[C/T]GTTTCCATTTCCTTC	84132
rs765874988	in-del	-/TGG	3.3534e-05	0.00409461	intron-variant	USP42	GRCh38.p7	7:6156705	TCCAGGGTCTGCTGC[-/TGG]TGGTTTTGTGTTTTA	84132
rs765878422	in-del	-/TTTATTT			intron-variant	USP42	GRCh38.p7	7:6083263	TTATTTATTTATTTA[-/TTTATTT]ATTTTAGATACAGTC	84132
rs765903001	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130099	CAAGCAGTCCTCTTG[C/T]GTCGACCTCCGAAAG	84132
rs765903306	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120586	ATTTCAGGCATGAGC[C/T]ACTATGCCTGGCCTA	84132
rs765906483	snp	A/T	0.0032137	0.0399565	intron-variant	USP42	GRCh38.p7	7:6111789	TTTTTTTTTTTTTGT[A/T]TTTTTAGTAGAGACG	84132
rs765907541	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6149294	CTCCATGCCACAGGT[C/T]CTGCTGATTTCGATC	84132
rs765912370	snp	A/G	1.65633e-05	0.00287774	missense	USP42	GRCh38.p7	7:6149865	CCCGTTCCCTCTTCT[A/G]CCATTACCAATTCTG	84132
rs765930791	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6094590	GATTATGTTTGCAGT[A/G]GTTCATTGTCACCTA	84132
rs765930900	snp	A/G/T	0.000132548	0.00813989	missense	USP42	GRCh38.p7	7:6145582	AACGGAGAGCCAATT[A/G/T]TCTACGTCTTGTATG	84132
rs765942619	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6112320	TGGGCATGGTGGTGT[G/T]TGCCTATAATCCCAG	84132
rs765943167	snp	C/T	5.34793e-05	0.00517076	missense	USP42	GRCh38.p7	7:6154000	GGGGACACAGCACCC[C/T]CTGACCTGTGTGATC	84132
rs765970202	snp	C/T	7.07526e-05	0.00594738	missense	USP42	GRCh38.p7	7:6154028	ATCCCGGGAGCTTAA[C/T]AGGCGATGCGAGCCC	84132
rs765999713	snp	C/G	1.65625e-05	0.00287766	missense	USP42	GRCh38.p7	7:6149812	AGTGTCAGTCTCAAC[C/G]TAACCTTCATAGTAA	84132
rs766026146	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6152924	CGAGAGGAAAGGAGG[A/C]GGCCCTGTCATCACT	84132
rs766061626	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6149181	TACTCTCCGCCCACG[C/T]GACCGTCTCCTTTGC	84132
rs766064988	in-del	-/AC			intron-variant	USP42	GRCh38.p7	7:6083677	GAGATATGTATATAT[-/AC]ACACACACACACACA	84132
rs766066890	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6121103	TAAAGATAATTTTAC[A/T]TCTCCATTTCCAGTC	84132
rs766087272	snp	C/T	3.16331e-05	0.00397687	intron-variant	USP42	GRCh38.p7	7:6156721	GGTGGTTTTGTGTTT[C/T]AGGGTTTTGAATTCT	84132
rs766104820	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6111078	TAGGGTAAGGAGATT[C/G]CTTTTCTCACCTGAT	84132
rs766136805	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6145147	GACCAGCCTAGCCAA[G/T]ATGGTGAAACCCCTG	84132
rs766147927	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6117155	GAACATGTTCATCAC[A/C]CTCAAAAGTTCCCCG	84132
rs766184986	snp	A/C	2.23736e-05	0.00334459	missense	USP42	GRCh38.p7	7:6153816	GCCTCAGCCTGGCAG[A/C]CCCGCCGCCGAATCC	84132
rs766223149	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6093379	CAACCTCCACCTCCC[A/G]AGTTCAAGTGATTCT	84132
rs766227518	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6090647	TTGAGCCTAGGAGGC[A/G]GAGGTTGCAGTGAGC	84132
rs766242885	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6148056	AAATATACAGAAAAC[C/G]GCCGAGCGCAGTGGC	84132
rs766243267	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6128796	TTTCAAAATTACATC[A/G]TTTTGCTTTACTTGA	84132
rs766249632	snp	C/T			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161623	ACTCCTTCCTGTCAT[C/T]ATCTGAATTCACTTT	84132
rs766257526	snp	A/G	1.73471e-05	0.00294504	missense	USP42	GRCh38.p7	7:6147747	TTTCCAGGTCCCATG[A/G]TGTGAAAAATGGAGG	84132
rs766262588	snp	A/T	1.85231e-05	0.00304323	missense	USP42	GRCh38.p7	7:6154187	TTCACCCCAGCGGGG[A/T]CCACGCCCGGGACGC	84132
rs766280588	snp	A/G	1.65795e-05	0.00287914	intron-variant	USP42	GRCh38.p7	7:6150518	TGAGGTAACGTAAGA[A/G]TACATCTGAGGCACG	84132
rs766297265	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6115921	CTGGACAACATAGTA[A/C]GACCCCATCTCTACT	84132
rs766298505	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6139341	TCTGCCTCTTCCTTA[A/G]GTGATGTGCATTATT	84132
rs766327380	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103682	GAGGTGGGACAATCG[C/T]TTGATCTCAGAAGTT	84132
rs766341836	snp	A/C/G	8.32153e-05	0.00644993	intron-variant	USP42	GRCh38.p7	7:6143022	TGCAGCAAGTACGTT[A/C/G]GGTGGTGACTTGATT	84132
rs766370206	snp	C/T	1.68301e-05	0.00290082	missense	USP42	GRCh38.p7	7:6149956	TCCCCCGCAGTGAAT[C/T]CTGCTCCCAGCCCGT	84132
rs766404079	in-del	-/TTTG			intron-variant	USP42	GRCh38.p7	7:6151438	AAAATAACTTCTTTT[-/TTTG]TTTGTTTTTTTGTTT	84132
rs766415030	snp	C/T	1.73809e-05	0.0029479	intron-variant	USP42	GRCh38.p7	7:6116749	TAGGGGTGTTTGTTA[C/T]GCCAGAATTAACGTT	84132
rs766417741	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6106385	TATGCAGAGTGCCAC[A/G]GTGTCTAAATAGTGA	84132
rs766433017	snp	C/T	1.76537e-05	0.00297095	missense	USP42	GRCh38.p7	7:6153880	AGCACCAAGAAGGCT[C/T]CGCCGCCCCGCGATC	84132
rs766451435	snp	A/C/T	0.000113344	0.00752736	synonymous-codon	USP42	GRCh38.p7	7:6153906	CGATCCCGGCACCCC[A/C/T]GCTACCAAAGAAGGC	84132
rs766455385	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6096522	ATGGTCATGCAGAGA[A/G]TTCACTCAGGTTCAT	84132
rs766458780	snp	G/T	1.82667e-05	0.00302209	synonymous-codon	USP42	GRCh38.p7	7:6154140	GGCTCCGCCTGCGCG[G/T]TCGGAGGAGCCCTGC	84132
rs766575245	in-del	-/TT/TTT			intron-variant	USP42	GRCh38.p7	7:6126284	ATGGATACGCCACAG[-/TT/TTT]TTTCTTTTTTTTTTT	84132
rs766579689	snp	C/T	3.33139e-05	0.00408116	intron-variant	USP42	GRCh38.p7	7:6142927	TGTGCCTCTTCTCTT[C/T]CCAGGCTGCTCAGAG	84132
rs766579817	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6148320	CCAGCCTGGGCAACA[C/G]AGTGAGACCCCGTCT	84132
rs766589310	snp	G/T	0.000147984	0.00860058	missense	USP42	GRCh38.p7	7:6154907	GCCCCAGCAGCCCCC[G/T]CGCAGGCGCGCCCCA	84132
rs766625917	snp	C/T	4.68417e-05	0.00483928	missense	USP42	GRCh38.p7	7:6154288	GCCCCGGCCGGTCAC[C/T]CGGAAGGGGACGCTG	84132
rs766637263	in-del	-/TATT			intron-variant	USP42	GRCh38.p7	7:6085107	TGTTTTAGCCATTCC[-/TATT]TATTTATTTATTTAT	84132
rs766662211	snp	G/T	1.74558e-05	0.00295425	intron-variant	USP42	GRCh38.p7	7:6149561	CTGGAGCTCTGACCA[G/T]GTGCGCTCTGCTTAC	84132
rs766677830	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6132986	CAGCACTGTTTTTAT[C/T]TCCAGTGCTTTTAAG	84132
rs766687557	snp	A/C/G			utr-variant-3-prime	USP42	GRCh38.p7	7:6161188	GATTTGTAAAGCCGA[A/C/G]AGTATGTTTCTATTA	84132
rs766691478	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6159140	GCCCCTTGTCTTTCT[C/G]TTTCAAACTCCTCCT	84132
rs766713542	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6151237	AGGCCTGGGACGGTA[A/C]ACTACTGTAGACTCT	84132
rs766713746	snp	A/G	5.22753e-05	0.00511223	intron-variant	USP42	GRCh38.p7	7:6139063	ATTACGTGTAATGAT[A/G]AAGCCTTGTCTTTAC	84132
rs766714572	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6091384	GGCATGCATCATCAT[A/G]CCCACCTAATTTTTT	84132
rs766755385	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6159700	CACCTCATCACGTTT[C/G]CATTACTGGCTGGGG	84132
rs766773773	snp	C/T	0.000120113	0.00774868	intron-variant	USP42	GRCh38.p7	7:6150339	CAGCCTCGTTTGTGG[C/T]GGTTCCCTTGGCTGG	84132
rs766792219	snp	C/G/T	3.42168e-05	0.00413611	missense	USP42	GRCh38.p7	7:6154969	CACGACAGAACTGCA[C/G/T]TTGTAGCCGGAGACA	84132
rs766801728	snp	C/T	0.000111442	0.00746381	missense	USP42	GRCh38.p7	7:6135948	GTCATCAATGAGATG[C/T]GGCGTAAGTATTAAC	84132
rs766818114	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6142709	GGGAATATAGTGAGA[A/C]CCCTGTCTCTACAAA	84132
rs766826734	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6144785	TGAGGCAGGAGAATC[A/G]CTTGAACCTAGGAGG	84132
rs766826780	in-del	-/CTTA			intron-variant	USP42	GRCh38.p7	7:6122115	ATTCCATTTCTTCTG[-/CTTA]CTTTGGATTTAATGT	84132
rs766843998	snp	A/G	8.83462e-05	0.0066457	missense	USP42	GRCh38.p7	7:6154039	TTAACAGGCGATGCG[A/G]GCCCGTTGTCCCAGG	84132
rs766877516	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6126499	ACCGTGTTAGCCAGG[A/G]TGGTCTCTATCTCCT	84132
rs766879427	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151861	ACACTCACGAGGCAC[A/G]CGTTGCCCTTGGACT	84132
rs766881102	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6141688	CTCAGCCTCCCTAGT[A/C]GCTGGGACTACAGCG	84132
rs766892753	in-del	-/G	1.73803e-05	0.00294785	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116882	CCAGCACTAGCACCT[-/G]GGACAGCAAGAGAGA	84132
rs766902750	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6108634	TACAGACACGCACCA[C/T]CATGCCCAGCTAATT	84132
rs766940088	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130140	GTAGGCATGAGCCCC[C/T]GCGCCTGGCCATGGA	84132
rs766957923	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6118781	CACCTTTATCAAAAA[C/T]CAGGTGATTGAAGCA	84132
rs766988742	snp	A/C/G	8.80941e-05	0.00663621	missense	USP42	GRCh38.p7	7:6155144	CAAAGAAGCACAAAA[A/C/G]ATCAAAGAAGAAAAA	84132
rs767009802	snp	A/G	1.65605e-05	0.0028775	missense	USP42	GRCh38.p7	7:6149721	AACTGGTCAGTTAAT[A/G]GGTCCTCAGTGATCC	84132
rs767024148	snp	G/T	8.28123e-05	0.00643423	missense	USP42	GRCh38.p7	7:6149794	ACAAGTTGCCTGTTC[G/T]CCAGTGTCAGTCTCA	84132
rs767034319	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6121919	TCCCCGCTTGGCCTC[C/T]AAAAGTGCTAGGATT	84132
rs767035425	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6146436	CGGCCAAGATGGAAG[C/G]ATCACTTGAGCCCAG	84132
rs767049804	snp	C/T	1.65762e-05	0.00287886	intron-variant	USP42	GRCh38.p7	7:6150511	GATGAAATGAGGTAA[C/T]GTAAGAGTACATCTG	84132
rs767072376	snp	C/T	0.000351679	0.0132558	synonymous-codon	USP42	GRCh38.p7	7:6154407	AAAGGTGGACCGAGG[C/T]CACTACCGCAGCCGG	84132
rs767075143	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6101763	GTTCTGGGTAGACAA[C/T]GCCAAGAGATGATTT	84132
rs767120012	snp	A/G	6.62559e-05	0.00575531	missense	USP42	GRCh38.p7	7:6150467	TCTTAGAGACCTTCA[A/G]GCTTAGCAACAAACT	84132
rs767133269	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6158973	CTGTGTTTCCGTCCC[C/T]GTCCCACTGCACCGA	84132
rs767141836	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159906	GTCCGTCCCGTCCCC[C/T]GTGCTGCTGTCTGCG	84132
rs767144488	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6147245	TTCCACAGTGGCATA[C/T]ATTTATAATTAGAAA	84132
rs767183385	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6140236	AAATGATACACACAT[A/G]TGGTTAAAAAATGGT	84132
rs767193800	snp	C/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113462	CTTTTCTGGGGCTCT[C/T]ATCTCATTCTCCACA	84132
rs767217204	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6136996	TTGGTGGATAAATTT[A/T]ACTTTTTTCTATTTA	84132
rs767224070	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6094084	AGACGGGGTTTCACC[A/G]TGTTGGTCAGTCTGG	84132
rs767241358	snp	A/G	1.95417e-05	0.00312578	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111198	AGAATCAGCCTGGCA[A/G]CTCCGAGGCAGTCTC	84132
rs767243418	snp	C/T	1.65611e-05	0.00287755	missense	USP42	GRCh38.p7	7:6140130	CAACGTTTTTCAGAT[C/T]AGACAGACACACCCA	84132
rs767244527	snp	G/T	1.82174e-05	0.00301801	missense	USP42	GRCh38.p7	7:6154135	AGTCCGGCTCCGCCT[G/T]CGCGGTCGGAGGAGC	84132
rs767252040	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6101060	TTTGGCCTTGAGGGG[A/G]GCGCTCTAGGGAGGA	84132
rs767271007	snp	A/C	1.76058e-05	0.00296692	intron-variant	USP42	GRCh38.p7	7:6147735	TCGCTCTCCTTGTTT[A/C]CAGGTCCCATGATGT	84132
rs767307650	snp	A/G	1.79952e-05	0.00299954	intron-variant	USP42	GRCh38.p7	7:6147693	AATGAATCTCTCCTA[A/G]GGAGGTGTCCTGTGT	84132
rs767350675	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6079348	CTGTAATCCCAGCTA[C/T]GCTGGAGGCTGAGGC	84132
rs767366238	snp	A/T	3.04067e-05	0.00389903	missense	USP42	GRCh38.p7	7:6154697	GCTGGGGCCGGGAGA[A/T]GTTCTACCCCGACAG	84132
rs767414013	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151086	TATTTGTGTATCTAA[A/G]CATAGAAAAGGGACA	84132
rs767429370	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6106469	ACATACCATATAAGA[A/G]ACTGGGAATTTTAAA	84132
rs767446529	snp	A/T	1.73788e-05	0.00294772	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116816	ATTCATTCCCCACAG[A/T]CAGCTTTCCTATCAC	84132
rs767452368	snp	C/G			missense	USP42	GRCh38.p7	7:6155119	AAGGATCCTCTAGAA[C/G]AGCCTAAAGCAAAGA	84132
rs767461178	snp	A/C/T	8.32915e-05	0.00645288	missense	USP42	GRCh38.p7	7:6147885	AGCTTCCCTCTCACA[A/C/T]GATAAAGGTAACAGT	84132
rs767472622	snp	C/G	3.82951e-05	0.00437562	intron-variant	USP42	GRCh38.p7	7:6140036	GTTTGAATTCTTGAT[C/G]TTTTGTGAGCTCCCA	84132
rs767496178	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098889	CCTCATTTGAGGTGT[C/T]TGCATAGTCTTCGGG	84132
rs767531196	snp	A/G	9.17137e-05	0.00677115	missense	USP42	GRCh38.p7	7:6154960	CGCTTCTCCCACGAC[A/G]GAACTGCACTTGTAG	84132
rs767531389	snp	A/G	5.57678e-05	0.00528023	synonymous-codon	USP42	GRCh38.p7	7:6154242	CGCACCCGAGGCCGC[A/G]GAGCGGCCGCCAGCT	84132
rs767534508	in-del	-/T	1.65787e-05	0.00287907	intron-variant	USP42	GRCh38.p7	7:6145499	GAAATGTTTCTCCTG[-/T]TTCCATTTCCTTCTA	84132
rs767547107	snp	A/G			synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111301	ACTTTCTTTAGGACC[A/G]GTACCTGGTGCTGTA	84132
rs767553921	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6137204	AACTGTAATCTTTTT[G/T]CCTAGAAAGCCACTG	84132
rs767578719	in-del	-/A			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080223	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	84132
rs767586296	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6085108	TGTTTTAGCCATTCC[C/T]ATTTATTTATTTATT	84132
rs767609182	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6107609	AGACGGGATTTCTCC[A/T]TGTTGGTCAGGCTGG	84132
rs767633887	snp	C/T	1.83182e-05	0.00302635	synonymous-codon	USP42	GRCh38.p7	7:6157027	GGAAAGCAGGGATGA[C/T]AGGTGTCGTCTCTTT	84132
rs767652624	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080737	TCATATCTCTTTTTC[C/T]GTAACTTTTAAAATC	84132
rs767677794	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6115946	TCTACTAAAAATAAA[A/G]ATAAAAATTAGTCTA	84132
rs767728282	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6139516	TCCTTTCTAGTTGTG[C/T]CTGACATTTTCTTTT	84132
rs767730861	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159412	CTGGCGATTTTGCAA[C/T]CATCATTAAAATCTC	84132
rs767761898	snp	C/T	2.80721e-05	0.00374637	intron-variant	USP42	GRCh38.p7	7:6135815	TTGTATTTTGCTAAT[C/T]TGGAGGATTATCATC	84132
rs767786295	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077047	GCCCAGCTAATTTTT[A/G]TATTTTTAGTAGAGA	84132
rs767786557	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6138716	GTCAGATCAATGGCA[A/G]CATTAGATTCTCATA	84132
rs767790736	snp	A/G	0.000181967	0.00953679	missense	USP42	GRCh38.p7	7:6154874	GCTGCGAGCCGGCCC[A/G]GGAGAGGGAGCGGCA	84132
rs767795305	snp	G/T	1.69152e-05	0.00290814	missense	USP42	GRCh38.p7	7:6150261	CAGCCTGCCCTGCAC[G/T]CAGAAAATCCCTTTG	84132
rs767804757	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6146751	GAGTTTGCTCCGCAT[C/T]GCACTCTGTGGCCAT	84132
rs767842260	snp	A/G	1.65636e-05	0.00287776	missense	USP42	GRCh38.p7	7:6145571	TGTCTCAACCCAACG[A/G]AGAGCCAATTGTCTA	84132
rs767880183	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077764	CAATCTCATCTCACT[A/G]CAACCTCCACCTTCC	84132
rs767881377	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6092865	TAATGTCTTATGTTG[C/G]TGTGCAGGGAAGTGG	84132
rs767902955	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6152592	TGGGCAGGGAACACT[A/C]ATTCCCAACCTAAGG	84132
rs767952471	snp	C/T	4.09727e-05	0.004526	missense	USP42	GRCh38.p7	7:6154489	GAGGGCCACCGTCAC[C/T]GGCGGCGCCGCACCT	84132
rs767954743	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6133094	CTTAGATCTGTACAT[A/G]TATTATTTCTGTCAA	84132
rs767962857	in-del	-/TTTTG			intron-variant	USP42	GRCh38.p7	7:6125752	GGTATTTTTCCTTAC[-/TTTTG]TTTTGTTTTGTTTTT	84132
rs767969992	snp	A/C	1.8571e-05	0.00304715	missense	USP42	GRCh38.p7	7:6135918	AATCCTGGGGACGTT[A/C]TTAAACCAATGTTTG	84132
rs768014206	in-del	-/TTTG			intron-variant	USP42	GRCh38.p7	7:6128709	TTTAATGTTTTGTTT[-/TTTG]TTCTGTTCTTTTTTA	84132
rs768025963	snp	A/G	7.10353e-05	0.00595925	missense	USP42	GRCh38.p7	7:6150144	GAGGCCACTCCGCAC[A/G]AGCTTCAAGAACCCA	84132
rs768026943	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6123641	GCACTCCAGCCTGGG[C/T]GACAGCGAGACTCCA	84132
rs768042100	snp	G/T	4.76588e-05	0.0048813	missense	USP42	GRCh38.p7	7:6154730	CGCGCTGGGACAGGT[G/T]CCGGTACTACCATGA	84132
rs768077561	snp	A/T	0.000109821	0.00740934	intron-variant	USP42	GRCh38.p7	7:6144061	TATTCGTCTTCTTAT[A/T]CTTTTGTTTCTGTTT	84132
rs768123349	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6109432	GGCAGAGTCTCTCTA[A/T]GTCAGTCTGGAGTGC	84132
rs768130585	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6157648	TAAAGCATTTTTGAT[A/G]GAAATACTTTTGCAG	84132
rs768154668	in-del	-/TT			intron-variant	USP42	GRCh38.p7	7:6128676	TTGATATTTTAAGAC[-/TT]AAGGCTTATTCTGCC	84132
rs768176081	snp	A/G	1.93527e-05	0.00311062	synonymous-codon	USP42	GRCh38.p7	7:6153960	CCCCGAGGAGCCTCC[A/G]CCCAGCGCCGGCGAG	84132
rs768219419	snp	A/C	0.000155921	0.00882815	synonymous-codon	USP42	GRCh38.p7	7:6154791	GAAGCCCTTCCACGG[A/C]GGCCGCGAGCACGAG	84132
rs768236448	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6115792	TGGTTTTCTACACTT[-/A]ACTAAAAAAATGTGA	84132
rs768237262	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136386	ATACATTTTGTCGTA[C/T]GTGGCTATGTCTTTG	84132
rs768244961	snp	C/T	1.73815e-05	0.00294795	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116886	GCACTAGCACCTGGA[C/T]AGCAAGAGAGAGGAC	84132
rs768255907	snp	C/G/T	8.86162e-05	0.00665591	intron-variant	USP42	GRCh38.p7	7:6147725	ACCCTAAGTATCGCT[C/G/T]TCCTTGTTTCCAGGT	84132
rs768288569	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6134171	GCTGGGATTACAGGT[A/G]TGAGCCACCAGGCTC	84132
rs768310413	in-del	-/TACTA			intron-variant	USP42	GRCh38.p7	7:6136665	GGTGAATGAATACTT[-/TACTA]TACGCAGTGACAGAA	84132
rs768328292	snp	A/T	4.01695e-05	0.00448142	missense	USP42	GRCh38.p7	7:6153901	CCCCGCGATCCCGGC[A/T]CCCCCGCTACCAAAG	84132
rs768329410	snp	A/G			synonymous-codon	USP42	GRCh38.p7	7:6154065	CCAGGACGCAAAGGG[A/G]ATGATCGCGGAGGGC	84132
rs768337606	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6084350	GGTTTTGATCTATTG[C/T]AGGTTTCCAGTAACT	84132
rs768338197	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6118416	AGTCCCAGCTACTTG[A/G]GAGACTGAGGTGGGA	84132
rs768343811	snp	C/G	3.32513e-05	0.00407732	missense	USP42	GRCh38.p7	7:6147787	TCATCCCACCCATAG[C/G]CCCGGCCAGTCCTCT	84132
rs768363574	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6148922	TTGGCATTGCTTTTC[C/T]AAAGCCTGTTTTTGT	84132
rs768408122	snp	C/T	3.31301e-05	0.00406989	missense	USP42	GRCh38.p7	7:6149641	CAAGCAGTTCCATGT[C/T]GAGTCCTAACGGGAA	84132
rs768433235	snp	C/T	1.69413e-05	0.00291039	missense	USP42	GRCh38.p7	7:6154367	CAGGCCCTTCCCCAG[C/T]GAAGGAGAAAATCGG	84132
rs768433662	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6084720	ATATCGCAAGGACTC[-/T]TTTTTTTTTTTTTTT	84132
rs768458637	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6109024	ACAGCTGTGGAGTAG[A/G]TGCCAGCACAGTACC	84132
rs768465031	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152388	AGTGTCAGTGAAAAC[C/T]GTGCCAGTGACACAC	84132
rs768466240	snp	A/G	3.30038e-05	0.00406212	intron-variant	USP42	GRCh38.p7	7:6157084	CTTGGAATTAGGAAG[A/G]TAGAAACTATTTCTT	84132
rs768494973	in-del	-/TTTGTTTCTG	2.69299e-05	0.00366936	intron-variant	USP42	GRCh38.p7	7:6144064	TCGTCTTCTTATACT[-/TTTGTTTCTG]TTTGTTTCAAGGTGT	84132
rs768495952	snp	A/T	2.79334e-05	0.0037371	intron-variant	USP42	GRCh38.p7	7:6144058	ATATATTCGTCTTCT[A/T]ATACTTTTGTTTCTG	84132
rs768509178	snp	C/T	0.00019115	0.00977437	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116802	TTTCTCAGTCCATAA[C/T]TCATTCCCCACAGAC	84132
rs768509595	snp	C/T	2.5646e-05	0.00358083	synonymous-codon	USP42	GRCh38.p7	7:6153933	AGGCGCCTGGGAGGC[C/T]ATGGCCGTCGCCCCC	84132
rs768524534	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6078651	CTTGTGAAAATTGTT[A/G]ATCTGGCTGGCTACC	84132
rs768541485	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6142427	TTTACCATGTTAGCC[A/C]GGATGGTCTGGATCT	84132
rs768567093	snp	G/T	2.26642e-05	0.00336624	intron-variant	USP42	GRCh38.p7	7:6144210	AGGTATGTGGATGAT[G/T]TCATTAATCATGTTT	84132
rs768605974	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6096841	GGCTTGCTGCTCACT[A/G]TACCAATCATGCCCA	84132
rs768626028	snp	A/G	6.64165e-05	0.00576228	missense	USP42	GRCh38.p7	7:6154321	CCTAGCCCCGGCGAG[A/G]GGGTCGAGGACGCCG	84132
rs768651723	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6132765	CAACCTCCGCCTCCC[A/G]GGTTCACGCCATTCT	84132
rs768710437	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151704	CGCTGTGGCCTCCCA[A/G]AGGGCTGGGATTCCA	84132
rs768755241	snp	C/T			utr-variant-3-prime, missense	USP42	GRCh38.p7	7:6160563	CTTTCAGATTCAACG[C/T]GTTCAACAGAAGCCA	84132
rs768772434	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6131907	TGTTTTTGAATGATA[C/T]TCTCATGGGGTGTAG	84132
rs768774514	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6143231	TGTGAAAGCCTGGGG[C/G]ATGACATTATTGGGC	84132
rs768775853	snp	A/C/T	3.68876e-05	0.0042945	missense, synonymous-codon	USP42	GRCh38.p7	7:6135914	CAGTAATCCTGGGGA[A/C/T]GTTATTAAACCAATG	84132
rs768791900	snp	C/G	1.68684e-05	0.00290412	missense	USP42	GRCh38.p7	7:6150253	GCCAAGGCCAGCCTG[C/G]CCTGCACTCAGAAAA	84132
rs768807809	in-del	-/TCT			intron-variant	USP42	GRCh38.p7	7:6092103	TCTTCTTCCTCCTCT[-/TCT]TCTTCTTCTTCTTCC	84132
rs768848227	snp	G/T	1.76836e-05	0.00297347	missense	USP42	GRCh38.p7	7:6154031	CCGGGAGCTTAACAG[G/T]CGATGCGAGCCCGTT	84132
rs768851041	snp	A/G	2.20968e-05	0.00332384	intron-variant	USP42	GRCh38.p7	7:6135995	TTGTATTTATTACCT[A/G]GTTATACTTTTTTTT	84132
rs768864760	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6126965	AATATATGAGAGTTC[C/G]AGCTTCCTTGCATCT	84132
rs768868380	snp	C/G	1.77212e-05	0.00297663	missense	USP42	GRCh38.p7	7:6154077	GGGGATGATCGCGGA[C/G]GGCCCGCGGGACTCG	84132
rs768918277	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6126232	CAGGTCGTTGCATGT[A/G]TTAATAATTCTTTCA	84132
rs768926689	in-del	-/TTCC	5.1909e-05	0.00509429	frameshift-variant	USP42	GRCh38.p7	7:6156983	GAAGGCGTCGGACCT[-/TTCC]GTGAGAAAACGAAAC	84132
rs768946748	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080140	AGCCAGGAGAATGGC[A/G]TGAATCCGGGAGGCA	84132
rs768965958	snp	A/G	9.9397e-05	0.00704902	missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115340	CTAGGTGATGGCATC[A/G]CTCCTCCACAGAAAG	84132
rs768975085	snp	A/G	0.000446728	0.0149387	intron-variant	USP42	GRCh38.p7	7:6153721	GCCTGTCAAGCCCAC[A/G]CTAACGGGCGTGTTT	84132
rs768988496	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6135214	GCACTGGCTTTCAAA[A/T]TTGAAAGAGTATGAT	84132
rs769016432	snp	A/C	1.73872e-05	0.00294844	intron-variant	USP42	GRCh38.p7	7:6150316	AGGTGAGTGCACGTC[A/C]GGGTCTTCAGCCTCG	84132
rs769017917	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6088310	CCCTAGGCTGGACTG[C/T]AGTGGTGCAATCTCG	84132
rs769090122	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120929	GGGTATTTTATTTTT[A/G]AAATTTCAACTTACT	84132
rs769107399	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6145845	GAGACTGAGGCTGGG[G/T]GATCACTTGAGGTCA	84132
rs769123110	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6095271	TTAGCAATAAGGGAA[C/T]CCTGAGGGTGCTTTA	84132
rs769128339	in-del	-/TA			intron-variant	USP42	GRCh38.p7	7:6083670	GTATATTGAGATATG[-/TA]TATATATACACACAC	84132
rs769137983	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6106251	GAAGGTTTTGTCTTT[G/T]TAAAGCGTGTGTGTT	84132
rs769153932	snp	A/G	2.6898e-05	0.00366719	missense	USP42	GRCh38.p7	7:6153929	AAGAAGGCGCCTGGG[A/G]GGCCATGGCCGTCGC	84132
rs769155683	snp	C/G	1.87876e-05	0.00306488	missense	USP42	GRCh38.p7	7:6154202	ACCACGCCCGGGACG[C/G]TCAGGACCCATCCCA	84132
rs769170841	snp	C/G	1.77184e-05	0.00297639	missense	USP42	GRCh38.p7	7:6154461	GCCCGCCAGAGAGAG[C/G]AGGAGCAAGACTGAG	84132
rs769201098	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6116612	GGAGAATTTAAATTG[A/G]TTCTTTTAAAACTGA	84132
rs769240562	snp	A/C	1.71563e-05	0.0029288	intron-variant	USP42	GRCh38.p7	7:6140878	TGCTGTAATGATTAT[A/C]CTTTGCTCATCTTTT	84132
rs769258477	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6086856	TCAGCCTCCCGAGTA[A/G]CTGGAATTACAGGCG	84132
rs769265774	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6139088	CTTTACCGAAATTTT[A/G]CAGGTATAGCTAGGC	84132
rs769271381	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6113291	ATCATGAAACACAAC[C/G]TAATCGAATGTTGCA	84132
rs769350693	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6155828	GCCATCATAACTCAC[A/T]GCAGCCTTGACCTCC	84132
rs769355823	in-del	-/AA			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103740	CCCCCGTCTCTACAA[-/AA]AAAAAAAAAAAAAAA	84132
rs769373909	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6140714	TTTTGATTCTAATCA[A/G]TAGTATATGAGGGGC	84132
rs769387578	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6117562	TAGGTAAATATCTAG[A/G]AGTAAAATGGCTTGG	84132
rs769399829	snp	G/T	1.77351e-05	0.00297779	missense	USP42	GRCh38.p7	7:6149997	AAATCCAAGCTGAAC[G/T]CCAGCGTGCTGGTGC	84132
rs769443634	snp	C/G	5.21354e-05	0.00510539	intron-variant	USP42	GRCh38.p7	7:6116786	GCCCTCATTTTCTCC[C/G]TTTCTCAGTCCATAA	84132
rs769454448	snp	A/T	1.76303e-05	0.00296898	intron-variant	USP42	GRCh38.p7	7:6149540	TCTGTTTGTGTGACC[A/T]TGTTTCTGGAGCTCT	84132
rs769458491	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6156176	AACCCTGGGAAAGAT[C/T]ACCAAAAGCCATATG	84132
rs769498530	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6139887	GCCTTGCTTCCCGAG[G/T]CCCTTCCTGACAGAC	84132
rs769524892	snp	G/T	4.21754e-05	0.00459194	missense	USP42	GRCh38.p7	7:6153898	CCGCCCCGCGATCCC[G/T]GCACCCCCGCTACCA	84132
rs769556202	snp	A/G	3.34487e-05	0.00408941	missense	USP42	GRCh38.p7	7:6156914	AGCTTGGAGACTGTC[A/G]CCCAGTTCCGGAGAG	84132
rs769613765	snp	G/T	8.13769e-05	0.00637823	missense	USP42	GRCh38.p7	7:6154994	GAGACAACTGTAACC[G/T]CTCTGATCGGTTTCA	84132
rs769619663	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6128140	TTACTTTTGTAGAGA[-/T]TTTGGTCTCGCTGTG	84132
rs769657350	snp	G/T	3.56926e-05	0.00422434	missense	USP42	GRCh38.p7	7:6154946	CCCCGCACCCCGACC[G/T]CTTCTCCCACGACAG	84132
rs769667432	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6149072	AGCAGCCATGGGGGA[A/T]CCTGCAGCGAGTCTC	84132
rs769677491	snp	A/C	1.65974e-05	0.0028807	synonymous-codon	USP42	GRCh38.p7	7:6147868	AGGCTTTATCGGACC[A/C]CAGCTTCCCTCTCAC	84132
rs769745067	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6132881	GTTTCACCGTGTTAG[C/T]CAGGATGGTCTCGAT	84132
rs769816827	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6133762	TGGGCTCAAGTGGTC[C/T]GCCTGCCTCAGCCTC	84132
rs769840226	snp	A/T			utr-variant-3-prime	USP42	GRCh38.p7	7:6161031	CTGATACTAGAAACT[A/T]ATTTGCTTATTTTAG	84132
rs769854294	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6143401	AGTCACTTTCTTCTG[A/G]GATAGGGAGGCTCCT	84132
rs769861744	in-del	-/ATTA			intron-variant	USP42	GRCh38.p7	7:6145905	TGAAACCCCGCCTCT[-/ATTA]AAAATACAAAAATTA	84132
rs769892717	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6151742	GCCACCGTGCCCGGC[C/T]AGCAGAGTCGTTTAT	84132
rs769893211	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120055	ACTGCAACCTACGCC[C/T]CCGGGTTCACGCCAT	84132
rs769901967	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6108467	TAGCATGGGTAGTAC[-/T]TTTTTGTACTTTTAC	84132
rs769902637	snp	A/G	0.000559503	0.0167164	synonymous-codon	USP42	GRCh38.p7	7:6154455	CGGGGAGCCCGCCAG[A/G]GAGAGCAGGAGCAAG	84132
rs769914663	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6136482	CAATATATTAAAGAC[G/T]ATTCAATTTAATATA	84132
rs769935631	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6127259	GTCTTCATCCACTTA[A/G]TGGTTGTTTTACAGA	84132
rs769983377	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6084141	AAGTGATTCTCCTGC[C/T]TCAGCCTCCTGAGTA	84132
rs769986959	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103396	AAAAAATTAGCCGGG[A/C]GTGGTGGCGGGCATC	84132
rs769989066	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6109251	AGGGACAAAAGAAAA[A/G]AAAACAAGACTTCAG	84132
rs770012084	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114308	CAAGGAATCAAATGT[A/G]TCTCATTTTTTCTAT	84132
rs770033103	snp	C/G	1.74081e-05	0.00295021	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116925	AATTCAGAAGCTCCC[C/G]ATGTCCAGAATTAGG	84132
rs770065022	snp	A/G	1.65616e-05	0.00287759	synonymous-codon	USP42	GRCh38.p7	7:6145533	TGTGAAATACCCTGA[A/G]TATCTTGATATTCGG	84132
rs770094962	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6119428	GTGAGCCATTATTGT[A/G]CAGGTACGCTGCAGC	84132
rs770103910	in-del	-/TTGT			intron-variant	USP42	GRCh38.p7	7:6133513	GTGTTTTTGTTATTG[-/TTGT]TTGTTTTTATTTTTT	84132
rs770125050	snp	G/T	1.71784e-05	0.00293069	intron-variant	USP42	GRCh38.p7	7:6140866	AGTAGTTGATGTTGC[G/T]GTAATGATTATACTT	84132
rs770129323	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126404	ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG	84132
rs770134513	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6088136	AAGACTTTGTCTCTA[C/T]GAAGTATTTAAAAAC	84132
rs770143151	snp	A/G	1.84228e-05	0.00303497	missense	USP42	GRCh38.p7	7:6154157	CGGAGGAGCCCTGCG[A/G]GCAGCCACTCCTTGT	84132
rs770154310	snp	C/T			synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111157	AGTTGACAAAGCTTC[C/T]GAATCTTCAGACCCA	84132
rs770164937	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077254	CACCCTGTATATAGT[A/G]ATTATCCATGAGAGG	84132
rs770172283	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6102855	GTCAAGTGATCTGAC[A/G]GTTTTTGGAAGACCA	84132
rs770179388	snp	A/G	0.000258065	0.0113563	missense	USP42	GRCh38.p7	7:6155195	GAGACCGCGACTCCA[A/G]GTGAGCCTGGGGCCT	84132
rs770193279	snp	C/G	1.65655e-05	0.00287793	missense	USP42	GRCh38.p7	7:6150439	CCTTTGCTGTCTCTC[C/G]CAGAAGACAAAATCT	84132
rs770193492	in-del	-/CTT			cds-indel	USP42	GRCh38.p7	7:6154782	CCGGGACTGGAAGCC[-/CTT]CCACGGCGGCCGCGA	84132
rs770194500	snp	C/G			utr-variant-5-prime	USP42	GRCh38.p7	7:6088808	TCCTGCTTGAAGCCT[C/G]AAGTGTTCCAAGCAT	84132
rs770207231	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6113385	ACGGCCTTCAACCTC[C/T]TGTCATGTTGCTGGG	84132
rs770212506	snp	A/C	2.17092e-05	0.00329456	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111281	AATGATGTGTCAAAT[A/C]ACACACTTTCTTTAG	84132
rs770250109	snp	A/G			utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081763	TGCGGGTTCGCTCCG[A/G]GCCGCTCCTCCCTGC	84132
rs770268812	snp	A/C/G	5.32962e-05	0.00516195	intron-variant	USP42	GRCh38.p7	7:6147723	TCACCCTAAGTATCG[A/C/G]TCTCCTTGTTTCCAG	84132
rs770331060	snp	A/T	0.000136808	0.00826955	missense	USP42	GRCh38.p7	7:6154726	AGGCCGCGCTGGGAC[A/T]GGTGCCGGTACTACC	84132
rs770337360	snp	C/T	1.81177e-05	0.00300974	missense	USP42	GRCh38.p7	7:6154127	AAGGGTTGAGTCCGG[C/T]TCCGCCTGCGCGGTC	84132
rs770337843	in-del	-/AA			intron-variant	USP42	GRCh38.p7	7:6153645	TAATAATAATAAAAT[-/AA]AGAGACGAAATAGCA	84132
rs770348434	snp	C/G/T	8.28516e-05	0.00643585	intron-variant	USP42	GRCh38.p7	7:6140094	GGAGTTTTTGCAAAG[C/G/T]TCTTCTCTCATGTCA	84132
rs770354814	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6137766	CTCACTGCAACCTCC[C/G]CCTCTCGGATTCCAG	84132
rs770365813	in-del	-/CAA			upstream-variant-2KB	USP42	GRCh38.p7	7:6078601	AGCAAGACTCCATCT[-/CAA]AAAAAAAAAAAAAAA	84132
rs770366063	snp	C/T	4.98981e-05	0.00499465	missense	USP42	GRCh38.p7	7:6149932	TTTCTAGTAAAGTAA[C/T]AAAACCGATCCCCCG	84132
rs770376315	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6141319	GCAATTCTTCTGCCT[C/T]AGCCTCCCGAGTAGG	84132
rs770385610	in-del	-/AGG			intron-variant	USP42	GRCh38.p7	7:6155484	CTTTATAACTCTTCC[-/AGG]AGGAGTAAGCATGCA	84132
rs770413354	snp	C/G/T	8.49169e-05	0.00651553	intron-variant	USP42	GRCh38.p7	7:6115534	AACATGTAAGTGTTC[C/G/T]GTGTTGTGTTTGTAG	84132
rs770461575	snp	A/G	1.66751e-05	0.00288744	missense	USP42	GRCh38.p7	7:6156900	TACCCAGGGTCACCA[A/G]CTTGGAGACTGTCGC	84132
rs770473851	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6092005	CTTCTTCTTCTTCTT[-/C]TTCTTCTTCTTCTTC	84132
rs770477780	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6136711	AAAGTTAATTAGGCT[A/G]CTCTGGACACACTGC	84132
rs770483825	in-del	-/TTAT			utr-variant-3-prime	USP42	GRCh38.p7	7:6160955	ATTTAATTTAAAGAC[-/TTAT]TTAAAAACTCACAAG	84132
rs770485640	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148047	CAGTATTTCAAATAT[A/G]CAGAAAACGGCCGAG	84132
rs770528585	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6097856	CGGCCTCCCAAAGTG[C/G]TGGGACTACAGGCGT	84132
rs770561370	snp	C/G	0.000132952	0.0081522	missense	USP42	GRCh38.p7	7:6153864	GGCCGCCGGCCTCAG[C/G]AGCACCAAGAAGGCT	84132
rs770566060	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6121824	TCACCACACACAGCT[A/C]ATTTTTAAATTATTT	84132
rs770567359	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6118373	TAAAAAATACAAAAA[C/T]TATCTGGGCTTGGCG	84132
rs770571280	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6155907	GGGACTGCAGGCGTG[C/T]GCTACCATCCTCAGC	84132
rs770574578	snp	A/G	0.00017411	0.0093287	missense	USP42	GRCh38.p7	7:6154838	AGCGGCCGCACAAGG[A/G]CCACAACCGGGGCCG	84132
rs770581933	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6107368	GGATTAACCTTTTCT[C/T]ATATTTCTTACAACT	84132
rs770597998	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6096190	ACATATAGGTATACC[G/T]GGCCAGGCGTGGTGG	84132
rs770604702	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6162020	TAAGAAAAAAAGTCA[A/G]TTTGTGGTTTCTGGT	84132
rs770615306	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6130648	GCCTGTTGAGTGTAA[C/G]TCAAGGCTGTTTACT	84132
rs770630420	snp	C/T	3.3123e-05	0.00406945	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115363	ACAGAAAGTTCTTTT[C/T]CCATCTGAGAAGATT	84132
rs770670124	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6087157	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATAAC	84132
rs770684869	snp	A/G	1.67621e-05	0.00289495	missense	USP42	GRCh38.p7	7:6150229	GCCTAGCGCCTGATG[A/G]TGCCAGCTGCCAAGG	84132
rs770706349	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077939	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGGG	84132
rs770718036	snp	A/G/T	3.31863e-05	0.00407336	intron-variant	USP42	GRCh38.p7	7:6150533	GTACATCTGAGGCAC[A/G/T]TGTGGCAGCATAGTA	84132
rs770779800	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6134818	TGAGACAGGGTCTCG[C/T]TCTGTTGCCCAGGCT	84132
rs770789648	snp	C/T	3.83054e-05	0.00437621	synonymous-codon	USP42	GRCh38.p7	7:6154932	GCCCCACGCCCTCGC[C/T]CCGCACCCCGACCGC	84132
rs770807025	snp	A/C	1.71108e-05	0.00292491	missense	USP42	GRCh38.p7	7:6150162	CTTCAAGAACCCATG[A/C]CCCTAAACGGTGCTA	84132
rs770811920	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6119342	CTCTGGGTGTGGCGG[C/G]AAGCGCTAGTCCTGG	84132
rs770829786	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6088156	TATTTAAAAACTAGC[C/T]GGGTACTGAGCTATG	84132
rs770831142	snp	A/G/T			intron-variant	USP42	GRCh38.p7	7:6158439	GCCTTTTGCTTCTCG[A/G/T]CTGAGTTGTGGGTTA	84132
rs770833114	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6113364	CCCACAGGACCTCTT[-/A]TCTCCACGGCCTTCA	84132
rs770838446	snp	C/T	6.62987e-05	0.00575717	utr-variant-3-prime, intron-variant	USP42	GRCh38.p7	7:6159485	AAAACAAAAAATTCA[C/T]TAGTTATGGTAAGCT	84132
rs770882227	snp	C/T	2.06031e-05	0.00320953	synonymous-codon	USP42	GRCh38.p7	7:6154222	GACCCATCCCAGAGC[C/T]TGGGCGCACCCGAGG	84132
rs770964455	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6144020	TAGTAACAAGAAAGA[C/T]CAAAATACCACAAAT	84132
rs770976252	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6095833	AGTGGTGTGGTCACA[C/T]CTCACTGCAGTCTAC	84132
rs770976513	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6117618	ATTTTAAGAGACTTC[C/G]AGACTTTCCAGAAGG	84132
rs770998487	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6110148	CTCCTGAAAGGTTTT[C/G]TACATAGGAGTGGCA	84132
rs771003286	snp	A/G	8.49509e-05	0.00651677	missense	USP42	GRCh38.p7	7:6154378	CCAGCGAAGGAGAAA[A/G]TCGGCAGCCTCAGAA	84132
rs771010299	snp	C/T	1.65814e-05	0.00287931	intron-variant	USP42	GRCh38.p7	7:6150409	TTTTTGTTTTTATTG[C/T]AGTTGATGCCTGCTC	84132
rs771012661	snp	A/G	1.65699e-05	0.00287831	missense	USP42	GRCh38.p7	7:6150493	AAACTGAAAGGCTCG[A/G]CGGATGAAATGAGGT	84132
rs771029485	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6117107	TTTGACATTTGTATA[C/G]ACCCGTGGAACTAGC	84132
rs771053020	in-del	-/ATT	1.7187e-05	0.00293142	intron-variant	USP42	GRCh38.p7	7:6140872	GATGTTGCTGTAATG[-/ATT]ATTATACTTTGCTCA	84132
rs771053737	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120117	CTACAGGTGCCTGCC[A/G]CCACGCCGGCTAATT	84132
rs771087038	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126433	GGGACTACAGGTGCC[C/T]ACCACCACGCCTGGC	84132
rs771091597	snp	A/T	0.000182923	0.00956181	intron-variant	USP42	GRCh38.p7	7:6140078	TCTGGTCACAGCATC[A/T]GGAGTTTTTGCAAAG	84132
rs771096721	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094041	GCGTGCCACCACACC[C/T]GGCTAATTTTTTTTG	84132
rs771102007	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6120799	CTGTTGGCCAAGCTG[G/T]TCTCGAACTCCTGGC	84132
rs771138117	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6148713	ATCTTCACAGCTTTT[C/T]GACTTGAGTTTGTTT	84132
rs771144608	snp	A/G	2.11463e-05	0.00325157	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111248	GGTTCTGCCAGCTGG[A/G]GTGCTGTGTCTTCAT	84132
rs771148935	snp	C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104381	CCACCGCGCCCGGCC[C/G]AGACCTTGTTTCTAA	84132
rs771170479	in-del	-/TTTTT			intron-variant	USP42	GRCh38.p7	7:6082616	TGTTTTTTTTTTTTT[-/TTTTT]TTTTTTTTTTTTGAG	84132
rs771176030	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6081880	TCCTGACTTTTATAT[G/T]CGTTAACACTAACAT	84132
rs771197004	snp	A/G	1.65625e-05	0.00287766	missense	USP42	GRCh38.p7	7:6149760	CCTAAGAAACAAAAA[A/G]TTACAATCAGTATTC	84132
rs771201994	snp	A/C			missense	USP42	GRCh38.p7	7:6156999	TCCGTGAGAAAACGA[A/C]ACACTTACGGATGGA	84132
rs771231128	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6148770	GCATGCTTTATTTTA[C/T]GGACATCAGGCAGTA	84132
rs771271310	snp	C/T	7.9852e-05	0.0063182	synonymous-codon	USP42	GRCh38.p7	7:6154674	CCACTACACCGAGGG[C/T]GAGCGTGGCTGGGGC	84132
rs771299731	snp	C/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113735	CACACCATTCTCCTG[C/T]CTCAGCCTCCTGAGT	84132
rs771302143	snp	G/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115095	TTAAATCTGTAACCC[G/T]CTCCCCTTTCTGTCC	84132
rs771306796	snp	A/G	2.97305e-05	0.00385543	synonymous-codon	USP42	GRCh38.p7	7:6146222	ATCGGTACTCAGCCA[A/G]CAAGCCTATGTGCTC	84132
rs771324237	snp	A/G	4.28918e-05	0.00463077	intron-variant	USP42	GRCh38.p7	7:6139226	GCCAGCCATGTCTTC[A/G]TTGGGGATCTCTGGT	84132
rs771327473	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6102974	GGTCAGGACAGCAGC[C/T]GCTGGGGAGGCCAGG	84132
rs771349535	snp	C/T			utr-variant-3-prime	USP42	GRCh38.p7	7:6161087	TTTATAGACAAGTTC[C/T]GTTTTTGAACTTTGT	84132
rs771381500	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6152521	GGTGGGAGTGCCCTC[A/G]CTGAGGCCCTCTGTT	84132
rs771423727	snp	A/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161968	AGATGTACATTATTT[A/T]CATATTACTATATTT	84132
rs771429506	snp	C/T	1.73936e-05	0.00294898	synonymous-codon	USP42	GRCh38.p7	7:6149987	GATGAATGGCAAATC[C/T]AAGCTGAACTCCAGC	84132
rs771464107	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6155994	ACCCCTAGACTCAAG[C/T]GATCCCAAAGCACTG	84132
rs771465577	snp	C/T	5.17942e-05	0.00508866	synonymous-codon	USP42	GRCh38.p7	7:6156976	GCCTCTGGAAGGCGT[C/T]GGACCTTTCCGTGAG	84132
rs771467580	snp	C/T	9.49713e-05	0.00689033	missense	USP42	GRCh38.p7	7:6154619	GCAGTCACCACCACT[C/T]CCGACACCGGAGCGG	84132
rs771476803	in-del	-/TCAC			intron-variant	USP42	GRCh38.p7	7:6147007	GGCTGCATACGCTTT[-/TCAC]TCACTCACTCGCTCC	84132
rs771494495	snp	C/G	0.000255918	0.011309	missense	USP42	GRCh38.p7	7:6153808	GACGCCGAGCCTCAG[C/G]CTGGCAGCCCCGCCG	84132
rs771551764	snp	G/T	0.000109961	0.00741405	intron-variant	USP42	GRCh38.p7	7:6141034	TAAAATAAGTCATTT[G/T]ATGTAACTGTAGTTC	84132
rs771585747	snp	A/G	0.00028928	0.0120232	intron-variant	USP42	GRCh38.p7	7:6140994	ATAAAGGTAAATTTC[A/G]TAATTATGGGAGTAA	84132
rs771589236	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6132288	CCTGTGCTGTGCCTG[A/T]TAAGAAGTCTGTTGT	84132
rs771614092	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6127353	CAAGTTTAATATCTC[C/T]TTGCCTAGCTCTTGA	84132
rs771614308	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138896	TCCCTGGTGCCCAAA[C/T]GGTTGGGGATTCTAG	84132
rs771624040	snp	C/T	3.17455e-05	0.00398394	missense	USP42	GRCh38.p7	7:6154259	AGCGGCCGCCAGCTC[C/T]TGTGCTGGACATGGC	84132
rs771673864	snp	A/G	6.70331e-05	0.00578896	synonymous-codon	USP42	GRCh38.p7	7:6150221	AGAAAACGGCCTAGC[A/G]CCTGATGGTGCCAGC	84132
rs771691715	snp	G/T	1.68783e-05	0.00290498	missense	USP42	GRCh38.p7	7:6140922	ATTTCAGTCAAATGT[G/T]TAAATTGCAAGGGCG	84132
rs771699551	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148080	CAGTGGCTCAAGCTT[A/G]TAATCCCAGCACTTT	84132
rs771710825	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6123131	GCACCTGGCCTGTTA[C/T]GCCCTCTTGATGAAC	84132
rs771719859	snp	A/G	1.65899e-05	0.00288005	missense	USP42	GRCh38.p7	7:6147795	CCCATAGCCCCGGCC[A/G]GTCCTCTCCCCGCCC	84132
rs771745159	snp	C/T	2.11017e-05	0.00324814	intron-variant	USP42	GRCh38.p7	7:6111417	CGCCAGAAACTCCTG[C/T]GTAAATGCTGCTGGG	84132
rs771749588	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6122680	TTCAACATGTTGGCC[A/T]GGATGGTCTCTTATC	84132
rs771808656	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6143902	ATGCTAATTAAGCAG[-/T]TTTCCCCCTGTATTT	84132
rs771819623	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6088575	TACTCTTATTACTCT[C/T]ATTGACAATCCTTCT	84132
rs771825982	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6156665	CACAGTGAATGTTCT[C/T]GGTGAATGGGTGGAA	84132
rs771851705	snp	A/G	1.80968e-05	0.003008	missense	USP42	GRCh38.p7	7:6153979	AGCGCCGGCGAGGAC[A/G]TCGTGGGGGACACAG	84132
rs771878094	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126156	GTGTTACGTGAATTA[C/T]ATAGTATGTAACCTT	84132
rs771893319	in-del	-/CCC	2.83082e-05	0.00376208	cds-indel	USP42	GRCh38.p7	7:6154902	GCACCGCCCCAGCAG[-/CCC]CCGCGCAGGCGCGCC	84132
rs771915578	snp	A/G	1.73869e-05	0.00294842	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116903	GCAAGAGAGAGGACC[A/G]AGACAAAATTCAGAA	84132
rs771917986	snp	C/G	1.72829e-05	0.00293959	missense	USP42	GRCh38.p7	7:6150150	ACTCCGCACGAGCTT[C/G]AAGAACCCATGACCC	84132
rs771952489	snp	C/G	0.000109069	0.00738395	missense	USP42	GRCh38.p7	7:6154451	CCAGCGGGGAGCCCG[C/G]CAGAGAGAGCAGGAG	84132
rs771967324	snp	A/G	1.78844e-05	0.0029903	synonymous-codon	USP42	GRCh38.p7	7:6135872	TTGTATGATGTGTAC[A/G]ATGCAAGCACATATT	84132
rs772024867	snp	A/G	1.6574e-05	0.00287867	utr-variant-3-prime, intron-variant	USP42	GRCh38.p7	7:6159478	CAGCCTCAAAACAAA[A/G]AATTCACTAGTTATG	84132
rs772025201	snp	A/G	5.03081e-05	0.00501513	missense	USP42	GRCh38.p7	7:6154733	GCTGGGACAGGTGCC[A/G]GTACTACCATGACAG	84132
rs772032854	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6100610	GCTGGGATTACAGGC[A/G]GGAGCCACTGTGCCT	84132
rs772036558	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6108421	GCAGCCAGTTTGGAA[A/C]GTACATGGGTATTTT	84132
rs772070164	snp	C/G	2.48419e-05	0.00352425	intron-variant	USP42	GRCh38.p7	7:6144222	GATGTCATTAATCAT[C/G]TTTTATGTCGAGCCT	84132
rs772074396	in-del	-/T	0.000367697	0.0135541	intron-variant	USP42	GRCh38.p7	7:6111109	GAAACAAATACATAC[-/T]TTTCATCTTTTGCAG	84132
rs772109073	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6158543	GGTAAACGGTCCTTA[C/G]AGTGTGTGAGAGAGA	84132
rs772152677	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6101221	CAGCAGCAGACAAGG[A/G]ATGGAAGCATCCGCC	84132
rs772172714	snp	A/G	7.97416e-05	0.00631383	synonymous-codon	USP42	GRCh38.p7	7:6155004	TAACCTCTCTGATCG[A/G]TTTCACGAACACGAA	84132
rs772194789	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151643	AGACAGGGTTTTACC[A/G]TGTTGGTCAGGCTGG	84132
rs772217532	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6125436	CGGGGGTTGCAGTGA[C/G]CCAAGAACACACCAC	84132
rs772247339	snp	C/G	1.75483e-05	0.00296207	intron-variant	USP42	GRCh38.p7	7:6149554	CATGTTTCTGGAGCT[C/G]TGACCAGGTGCGCTC	84132
rs772247694	snp	G/T	1.7978e-05	0.00299811	missense	USP42	GRCh38.p7	7:6154118	AAGCCCCGGAAGGGT[G/T]GAGTCCGGCTCCGCC	84132
rs772306485	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6087472	CTCCTGAGTAGCTGG[A/G]ACTACATGTGGATGC	84132
rs772312000	snp	G/T	5.02315e-05	0.00501131	missense	USP42	GRCh38.p7	7:6156863	AAATCAGAGGACTTT[G/T]TTAAAGATTCAGAAC	84132
rs772330324	snp	C/T	6.29822e-05	0.00561134	synonymous-codon	USP42	GRCh38.p7	7:6154608	TCTGGGCAGGTGCAG[C/T]CACCACCACTCCCGA	84132
rs772335451	snp	A/G	1.67122e-05	0.00289064	intron-variant	USP42	GRCh38.p7	7:6150384	GGAGCTGGCGACTGA[A/G]GCTGAAATATTTTTG	84132
rs772338459	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6134981	TTTTTGTAGAGACAG[C/G]GTTTGACCATGTTGC	84132
rs772355171	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6139812	CCTCCGCTCCCTTTC[C/G]TCCCACACAGGCCGC	84132
rs772372374	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6158990	TCCCACTGCACCGAT[A/G]ACAGGGTTTGCAGCT	84132
rs772384644	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094247	CGTGCCATAATAGCT[C/T]ACTGGACCCTTGACC	84132
rs772397133	snp	C/G	1.6591e-05	0.00288015	missense	USP42	GRCh38.p7	7:6149923	CGATGTCAGTTTCTA[C/G]TAAAGTAACAAAACC	84132
rs772420449	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6086197	CCTGCCACCTCACCT[-/G]GCTAATTTTTTTTTT	84132
rs772438081	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6105931	ATGTAAAGTCAATAC[C/G]CTGACAGCAAAACTG	84132
rs772457912	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148884	GGCAAACAGGAGGGC[A/G]TGTGCCCTGTAGGAA	84132
rs772473710	snp	C/T	3.67607e-05	0.00428707	synonymous-codon	USP42	GRCh38.p7	7:6154560	GCACCACCCCGGCCA[C/T]GGCGACAGGCTCAGC	84132
rs772486139	in-del	CTCTTCTTCTTCTTCTTTCTTCTTCTTCTCT/TC			intron-variant	USP42	GRCh38.p7	7:6092149	TTCTTCTTCCTCTTC[lengthTooLong]TTTTTTTTTTTTTTT	84132
rs772486573	snp	A/G	4.72088e-05	0.00485821	intron-variant	USP42	GRCh38.p7	7:6145690	CTATTAACTATTGTT[A/G]CATACATGCTATAAG	84132
rs772505163	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6129560	AGGCTCTGCCTCAGG[A/G]AAAAAAAAAAAAAAA	84132
rs772509071	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6144924	GTCTGTCCTTTGATG[G/T]GTTTGAAGAATTCAC	84132
rs772518846	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6128527	CATTTGAAGTGAGTT[A/T]TTCTGTAAACAGCGT	84132
rs772525190	snp	A/G	1.65638e-05	0.00287778	missense	USP42	GRCh38.p7	7:6149853	AACCCTACCAAGCCC[A/G]TTCCCTCTTCTACCA	84132
rs772547544	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6095234	GGATGTGGGTCAGGA[A/C]CAAAGGTATTAACTT	84132
rs772588747	in-del	-/G	1.65987e-05	0.00288082	intron-variant	USP42	GRCh38.p7	7:6140224	ATAAGTTGATAAAAT[-/G]GATACACACATGTGG	84132
rs772590085	snp	A/G/T	1.84224e-05	0.00303495	missense	USP42	GRCh38.p7	7:6153856	CCAGATGCGGCCGCC[A/G/T]GCCTCAGCAGCACCA	84132
rs772678246	snp	C/T	2.02887e-05	0.00318496	missense	USP42	GRCh38.p7	7:6156788	CTCTCAGCAGCGTGC[C/T]CTGACGCTGACCTCC	84132
rs772685356	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095294	GTGCTTTAGAGCTGC[A/G]TTAACTTGGACTCTG	84132
rs772709027	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6128662	TTTTAAGGTGATTAT[G/T]GATATTTTAAGACTT	84132
rs772710033	snp	A/G	1.65971e-05	0.00288067	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6115501	TGCCAATTACATGCT[A/G]TCACATGAACACTCC	84132
rs772710719	snp	C/G	0.000248725	0.011149	missense	USP42	GRCh38.p7	7:6153809	ACGCCGAGCCTCAGC[C/G]TGGCAGCCCCGCCGC	84132
rs772757880	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6106288	TATAACGGAAATGCT[A/G]TGAGAACGTGGATTA	84132
rs772760460	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6139254	GGTTGTAGTTTATTC[G/T]TATCAGAATTCATTT	84132
rs772767965	snp	G/T	1.69937e-05	0.00291488	intron-variant	USP42	GRCh38.p7	7:6142886	AAGACCCAAACACAA[G/T]TGACGGTGTGCGGTG	84132
rs772797219	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6079230	TTGGGAGGCCAAGGC[A/G]GGCGGATCACAAGGT	84132
rs772809737	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6107048	GTTATGTGTGTAGCA[A/G]ATGGAGTTTAGTTTG	84132
rs772820302	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6157691	TCTCCCGAATCCTTA[A/C]ACCTGTAGCATTCTG	84132
rs772822550	snp	C/T	2.12488e-05	0.00325944	intron-variant	USP42	GRCh38.p7	7:6111423	AAACTCCTGTGTAAA[C/T]GCTGCTGGGGCTTGG	84132
rs772825025	snp	C/G	3.31257e-05	0.00406962	missense	USP42	GRCh38.p7	7:6149793	AACAAGTTGCCTGTT[C/G]GCCAGTGTCAGTCTC	84132
rs772834644	snp	C/T	1.65745e-05	0.00287871	utr-variant-3-prime, intron-variant	USP42	GRCh38.p7	7:6159481	CCTCAAAACAAAAAA[C/T]TCACTAGTTATGGTA	84132
rs772866780	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6130017	TTGAGTCAGGGTCTT[A/T]CTTTGTTGTCCAGGC	84132
rs772903438	in-del	-/GT			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103557	CCTTTCTGTAACTCA[-/GT]GTGTGAGTCTGATGG	84132
rs772927145	snp	C/G	3.4366e-05	0.0041451	missense	USP42	GRCh38.p7	7:6150157	ACGAGCTTCAAGAAC[C/G]CATGACCCTAAACGG	84132
rs772966312	snp	A/G			missense	USP42	GRCh38.p7	7:6153974	CGCCCAGCGCCGGCG[A/G]GGACATCGTGGGGGA	84132
rs772970084	snp	A/G	0.000853898	0.0206451	synonymous-codon	USP42	GRCh38.p7	7:6154824	GGCCGGGCTGCACGA[A/G]CGGCCGCACAAGGAC	84132
rs772985478	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6094502	CAACTCCATTCTGTT[A/G]TGGATGTAGAAGAAC	84132
rs772997740	snp	A/C	1.74732e-05	0.00295572	synonymous-codon	USP42	GRCh38.p7	7:6147742	CCTTGTTTCCAGGTC[A/C]CATGATGTGAAAAAT	84132
rs773014963	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098438	CCTGGTCTTGCAGTT[C/T]CTTCAATTTTTGATT	84132
rs773056383	snp	C/T	0.000114685	0.00757163	missense	USP42	GRCh38.p7	7:6154210	CGGGACGCTCAGGAC[C/T]CATCCCAGAGCTTGG	84132
rs773094824	snp	C/T	0.000155622	0.00881968	missense	USP42	GRCh38.p7	7:6154735	TGGGACAGGTGCCGG[C/T]ACTACCATGACAGGT	84132
rs773096072	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6132894	AGCCAGGATGGTCTC[A/G]ATCTTCTACCTTGTG	84132
rs773101849	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6142601	AAAAATAAGGGGCAC[A/G]GCTGGGCATGACAGC	84132
rs773102276	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6156461	AAGGCAAACTTGTTA[A/G]ATTTTTGAGACAGGG	84132
rs773104529	snp	G/T	2.22844e-05	0.00333792	missense	USP42	GRCh38.p7	7:6153943	GAGGCCATGGCCGTC[G/T]CCCCCGAGGAGCCTC	84132
rs773124803	snp	C/G/T	0.000279652	0.0118215	missense	USP42	GRCh38.p7	7:6156996	CTTTCCGTGAGAAAA[C/G/T]GAAACACTTACGGAT	84132
rs773130454	snp	A/G	3.64299e-05	0.00426774	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111140	AGTTGAACAATGACC[A/G]TAGTTGACAAAGCTT	84132
rs773133044	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6112748	TTTTTTTTTAAGCTC[-/A]TTAGCTGTCGTTAGT	84132
rs773145027	in-del	-/C	0.000158894	0.00891189	intron-variant	USP42	GRCh38.p7	7:6155217	CTGGGGCCTTGTGCT[-/C]CCCGAGGCGCTGGCG	84132
rs773194602	snp	C/T	1.93575e-05	0.00311101	synonymous-codon	USP42	GRCh38.p7	7:6150107	GAGCTCCCACTCTCC[C/T]GGCCAAGATGCCGAA	84132
rs773233779	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6116727	ACCTAGAATCTCACC[A/G]CCTACCTAGGGGTGT	84132
rs773257533	snp	A/G	1.73875e-05	0.00294847	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116908	AGAGAGGACCAAGAC[A/G]AAATTCAGAAGCTCC	84132
rs773285720	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6124211	TCATGTTAGCATGAT[A/G]TATTTTTTCCATCTT	84132
rs773298770	in-del	-/G			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161587	CGTCTTTTTACTGTT[-/G]TTTTCCCCATTTGCT	84132
rs773356823	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6097108	ACGGGCTGCTATCAT[C/T]CTCTTTGCTACCAGA	84132
rs773365295	snp	C/G	1.75222e-05	0.00295986	intron-variant	USP42	GRCh38.p7	7:6149558	TTTCTGGAGCTCTGA[C/G]CAGGTGCGCTCTGCT	84132
rs773372354	in-del	-/AG	4.09333e-05	0.00452382	intron-variant	USP42	GRCh38.p7	7:6111390	GTACTGTTTTTCAAA[-/AG]AGAGAATTACCGCCA	84132
rs773415081	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6086757	TTGAGATGGAGTTTC[A/G]CTCTTGTCGCCCAGG	84132
rs773429246	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6101675	AGGAAAAGGGTCTCT[A/C]TGTTTGCTTTGATGG	84132
rs773432072	snp	G/T	1.72225e-05	0.00293444	missense	USP42	GRCh38.p7	7:6154961	GCTTCTCCCACGACA[G/T]AACTGCACTTGTAGC	84132
rs773451113	snp	A/G	3.31225e-05	0.00406941	missense	USP42	GRCh38.p7	7:6149649	TCCATGTCGAGTCCT[A/G]ACGGGAATTCCAGTG	84132
rs773459520	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6092470	AGGCATGCGCCACCA[C/T]GCCCGGCCTCAAGGA	84132
rs773460618	snp	C/T	1.77536e-05	0.00297935	missense	USP42	GRCh38.p7	7:6154084	ATCGCGGAGGGCCCG[C/T]GGGACTCGGCGTTGG	84132
rs773479121	snp	A/G	3.8246e-05	0.00437282	intron-variant	USP42	GRCh38.p7	7:6139214	GTACAACAGAGCGCC[A/G]GCCATGTCTTCATTG	84132
rs773487632	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6109319	TTATTAGGTCAGACA[A/G]TGTGAAGTCCAGACA	84132
rs773512015	snp	C/G/T	2.38906e-05	0.00345611	intron-variant	USP42	GRCh38.p7	7:6145691	TATTAACTATTGTTA[C/G/T]ATACATGCTATAAGA	84132
rs773537848	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6097564	GCATAAGCCACTGCG[-/C]CCCAGCCATGTGGGT	84132
rs773545313	snp	C/T	1.70124e-05	0.00291649	synonymous-codon	USP42	GRCh38.p7	7:6150272	GCACTCAGAAAATCC[C/T]TTTGCTAAGGCAAAC	84132
rs773547831	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6127279	TGTTTTACAGACAGA[A/G]GTTTTTAATTTTGGT	84132
rs773563237	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6113345	CTTCTCTCCAGCAGG[A/G]CTTTCCCACAGGACC	84132
rs773587078	snp	C/T	5.437e-05	0.00521364	synonymous-codon	USP42	GRCh38.p7	7:6154614	CAGGTGCAGTCACCA[C/T]CACTCCCGACACCGG	84132
rs773587647	in-del	-/T			frameshift-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6111216	CGAGGCAGTCTCACC[-/T]TGGAGACATGGATGC	84132
rs773591134	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114322	TATCTCATTTTTTCT[A/G]TTGATTGTATTATTT	84132
rs773607140	snp	A/C	3.63788e-05	0.00426475	synonymous-codon	USP42	GRCh38.p7	7:6154563	CCACCCCGGCCACGG[A/C]GACAGGCTCAGCCCT	84132
rs773635011	snp	A/C	1.74955e-05	0.00295761	intron-variant	USP42	GRCh38.p7	7:6150330	CAGGGTCTTCAGCCT[A/C]GTTTGTGGCGGTTCC	84132
rs773675337	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159660	CAGACCCAGGCCACG[C/T]GCTTGGGGACAGACC	84132
rs773702254	in-del	-/CTTG			intron-variant	USP42	GRCh38.p7	7:6128742	ATATGTCTGTGTTTT[-/CTTG]CTTCTCTGTGGGTTA	84132
rs773704397	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6136791	TAAATAAGGTTAATT[C/T]TCTTTTTTCGGTTCT	84132
rs773793703	in-del	-/TTTC			intron-variant	USP42	GRCh38.p7	7:6096915	GATGCCATCATTTTC[-/TTTC]TTTCTTTCTTTCTTT	84132
rs773800559	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6091332	TGGTCTCAAGCGATC[C/T]TCCCACCTCCGCCTC	84132
rs773823628	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6113407	GTTGCTGGGGCTTCT[C/T]TCTCTTCTTAGGACT	84132
rs773836842	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6129991	GCTGGATTTTAAAAC[A/C]ATTTTGTTTTTTGAG	84132
rs773850758	snp	A/G			missense	USP42	GRCh38.p7	7:6155072	AGAACAGTGACAGTC[A/G]TGTTGAAAAGAAAGC	84132
rs773869144	snp	C/T	1.83549e-05	0.00302937	missense	USP42	GRCh38.p7	7:6154168	TGCGAGCAGCCACTC[C/T]TTGTTCACCCCAGCG	84132
rs773871885	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6128705	CCATTTAATGTTTTG[-/T]TTTTTTGTTCTGTTC	84132
rs773887995	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6130100	AAGCAGTCCTCTTGC[A/G]TCGACCTCCGAAAGT	84132
rs773926720	snp	A/C/G			intron-variant	USP42	GRCh38.p7	7:6132146	GGCCAGGCTGGTCTC[A/C/G]AACTCCTAGGCTCAA	84132
rs773945031	snp	A/C/G	4.35249e-05	0.00466486	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111291	CAAATCACACACTTT[A/C/G]TTTAGGACCAGTACC	84132
rs773949073	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6141342	CGAGTAGGTGGGACT[A/G]TAGGTGCATGTGCCA	84132
rs773982368	snp	C/T	3.32094e-05	0.00407475	synonymous-codon	USP42	GRCh38.p7	7:6147790	TCCCACCCATAGCCC[C/T]GGCCAGTCCTCTCCC	84132
rs773992581	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6121830	CACACAGCTAATTTT[A/T]AAATTATTTTTGTAG	84132
rs773993350	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6125404	CTGAGGTGGGAGAAT[C/G]GCTTGAACCTTGGAA	84132
rs774024781	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6098050	GCTGGGATTACAGGC[A/G]CACACCACTACCCCA	84132
rs774129536	snp	A/G	3.67681e-05	0.0042875	missense	USP42	GRCh38.p7	7:6150016	GCGTGCTGGTGCCCT[A/G]TGGCGCCGAGTCCTC	84132
rs774145856	snp	A/G	6.72359e-05	0.00579771	intron-variant	USP42	GRCh38.p7	7:6157086	TGGAATTAGGAAGAT[A/G]GAAACTATTTCTTAA	84132
rs774175231	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6140090	ATCTGGAGTTTTTGC[A/G]AAGCTCTTCTCTCAT	84132
rs774210827	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096198	GTATACCTGGCCAGG[C/T]GTGGTGGCTCACGCC	84132
rs774225037	snp	C/T	1.68692e-05	0.00290419	synonymous-codon	USP42	GRCh38.p7	7:6150254	CCAAGGCCAGCCTGC[C/T]CTGCACTCAGAAAAT	84132
rs774233673	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6084183	AGGCATGAGCCACCA[C/T]GCCCAGCTAATTTTT	84132
rs774239025	snp	A/G	6.86083e-05	0.00585657	missense	USP42	GRCh38.p7	7:6154324	AGCCCCGGCGAGAGG[A/G]TCGAGGACGCCGCGG	84132
rs774251710	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138641	GTGGCCTGTTAGGAA[C/T]TGGGCTGCACAGCAG	84132
rs774259719	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6107409	TTCTTCTTCCTTTTC[-/T]TTTTTTTTTTTTTTT	84132
rs774260362	in-del	-/GCACGAGCGGGCCGGGCT	0.000162575	0.0090145	cds-indel	USP42	GRCh38.p7	7:6154799	CCACGGCGGCCGCGA[-/GCACGAGCGGGCCGGGCT]GCACGAGCGGGCCGG	84132
rs774262776	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6117162	TTCATCACCCTCAAA[A/T]GTTCCCCGATGCCCC	84132
rs774293860	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6105826	CATCTAGGACTTTAA[C/T]CCCTCTCACATGCAT	84132
rs774315768	in-del	-/TC	5.11823e-05	0.00505851	intron-variant	USP42	GRCh38.p7	7:6144070	TCTTATACTTTTGTT[-/TC]TGTTTGTTTCAAGGT	84132
rs774329014	snp	A/G	0.000255722	0.0113047	synonymous-codon	USP42	GRCh38.p7	7:6154368	AGGCCCTTCCCCAGC[A/G]AAGGAGAAAATCGGC	84132
rs774335010	snp	A/T	1.84371e-05	0.00303615	intron-variant	USP42	GRCh38.p7	7:6115564	GTATTGTAGTGCGCT[A/T]ACCTACTTTCATTTT	84132
rs774340248	snp	A/T	1.76375e-05	0.00296958	missense	USP42	GRCh38.p7	7:6157006	GAAAACGAAACACTT[A/T]CGGATGGAAAGCAGG	84132
rs774381626	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6081930	ATACAGTATACCTGT[A/G]TATGCAAGTTGCAGA	84132
rs774394168	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6137090	AACTTTTGCATCTTG[-/T]TAATTGAGTTGGAAT	84132
rs774408739	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6144805	AACCTAGGAGGCAGA[A/G]GTTGCAGTGAGCCGA	84132
rs774480740	in-del	-/TTGT			intron-variant	USP42	GRCh38.p7	7:6144447	AAAGTTCATTTTGTC[-/TTGT]TTGTTTGTTTTCTGA	84132
rs774488586	snp	G/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080677	CTGCACTCCAGCCTG[G/T]GCGACAGAGTGAGTC	84132
rs774491084	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098800	GTCTGTCTGCCTCGG[C/T]CTCTCAGAGTGCTGG	84132
rs774508720	snp	C/T	1.74105e-05	0.00295042	intron-variant	USP42	GRCh38.p7	7:6150321	AGTGCACGTCAGGGT[C/T]TTCAGCCTCGTTTGT	84132
rs774541656	in-del	-/AAA			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103756	AAAAAAAAAAAAAAC[-/AAA]AAAACTTAAAAAATT	84132
rs774571634	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6157205	GCCTGGTCTGGCCTC[A/G]GTGCTCATCCCTGCA	84132
rs774617998	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138060	AAGAAAATGTCATTG[C/T]TCTGTGTGTGTGTGT	84132
rs774622337	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6126532	CCTCGTGATCTGCCC[A/G]CCTCAGCCTCCCAAA	84132
rs774666725	snp	C/T	8.31428e-05	0.00644705	intron-variant	USP42	GRCh38.p7	7:6111404	AAGAGAGAATTACCG[C/T]CAGAAACTCCTGTGT	84132
rs774687741	snp	C/T	1.9525e-05	0.00312444	missense	USP42	GRCh38.p7	7:6154541	AGGACCGCCACGCCC[C/T]GGAGCACCACCCCGG	84132
rs774767617	snp	C/T	5.30509e-05	0.00515001	synonymous-codon	USP42	GRCh38.p7	7:6154032	CGGGAGCTTAACAGG[C/T]GATGCGAGCCCGTTG	84132
rs774802502	snp	A/G	3.5897e-05	0.00423641	missense	USP42	GRCh38.p7	7:6154466	CCAGAGAGAGCAGGA[A/G]CAAGACTGAGGGCCA	84132
rs774841261	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6127439	GTTACATTTAAGTCT[C/G]TGATCCATTTTGAGT	84132
rs774893947	snp	C/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6078100	GAGCCGAGATCGTGC[C/T]ATTGCACTCCAGCCT	84132
rs774904898	snp	C/G	2.4577e-05	0.00350541	missense	USP42	GRCh38.p7	7:6153796	CCCGAGGACCGCGAC[C/G]CCGAGCCTCAGCCTG	84132
rs774947364	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6120137	GCCGGCTAATTTTTT[G/T]GTATTTTTAGTAGAG	84132
rs774959874	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6125389	CAGCTACTTCGGAGA[A/C]TGAGGTGGGAGAATC	84132
rs774981405	snp	C/G	1.71752e-05	0.00293041	missense	USP42	GRCh38.p7	7:6153899	CGCCCCGCGATCCCG[C/G]CACCCCCGCTACCAA	84132
rs774999720	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6147272	GAAAAATATAAGCCT[A/G]GGCAACAAAGCGAGA	84132
rs775000672	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6119560	ACTTTGTGAATTTCT[A/G]CAAATAATCTTCCTG	84132
rs775012657	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6146591	ATTACCTGAGCCTGG[G/T]GAGGCCGAGGCTGCA	84132
rs775013607	snp	C/G	2.83378e-05	0.00376406	missense	USP42	GRCh38.p7	7:6154687	GGCGAGCGTGGCTGG[C/G]GCCGGGAGAAGTTCT	84132
rs775039960	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6155995	CCCCTAGACTCAAGC[A/G]ATCCCAAAGCACTGG	84132
rs775052897	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6134012	TCTCTTGCCTCAGCC[G/T]CCCGAGTAGCTGGGA	84132
rs775054680	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6122688	GTTGGCCAGGATGGT[C/T]TCTTATCTCCTGGCC	84132
rs775057001	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6128592	GTCTGTGTCTTTTAA[-/CT]CTCTGCTGCTCTAGG	84132
rs775068505	snp	C/G	1.73785e-05	0.0029477	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116796	TCTCCCTTTCTCAGT[C/G]CATAATTCATTCCCC	84132
rs775071035	snp	A/G	1.68539e-05	0.00290287	intron-variant	USP42	GRCh38.p7	7:6139243	TGGGGATCTCTGGTT[A/G]TAGTTTATTCTTATC	84132
rs775076907	snp	C/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115096	TAAATCTGTAACCCT[C/G]TCCCCTTTCTGTCCT	84132
rs775082284	snp	A/T	4.31863e-05	0.00464664	intron-variant	USP42	GRCh38.p7	7:6146269	GTCATGAAAACAAAT[A/T]GCCAGATTTTCTGGT	84132
rs775104012	snp	A/G	6.26468e-05	0.00559638	missense	USP42	GRCh38.p7	7:6154316	CTGAGCCTAGCCCCG[A/G]CGAGAGGGTCGAGGA	84132
rs775125730	snp	A/C/G	0.000602035	0.0173394	missense	USP42	GRCh38.p7	7:6154626	CCACCACTCCCGACA[A/C/G]CGGAGCGGGGTGGAG	84132
rs775160784	snp	A/G			downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161498	CTAAAGATTAAAAAA[A/G]CACTTGCCCCACTGT	84132
rs775234998	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6100660	ACTCTGTTTCTTAGG[G/T]ACTATTCTTGGTATC	84132
rs775241147	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6152627	GCCAGCTTGGACACT[C/G]GCTCCCTCGGCCAGG	84132
rs775249242	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6121969	TCTGTCTCCTTTTTC[A/G]TTTGATCAATCTGAC	84132
rs775262947	snp	C/T	5.01174e-05	0.00500561	missense	USP42	GRCh38.p7	7:6149944	TAACAAAACCGATCC[C/T]CCGCAGTGAATCCTG	84132
rs775296054	snp	C/G	8.6986e-05	0.00659435	intron-variant	USP42	GRCh38.p7	7:6115542	AGTGTTCCGTGTTGT[C/G]TTTGTAGTATTGTAG	84132
rs775301252	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6130803	GAAGACAAAGATTTT[A/G]TGCTCACAGGGCACA	84132
rs775318812	snp	A/G	0.00012313	0.00784537	missense	USP42	GRCh38.p7	7:6153875	TCAGCAGCACCAAGA[A/G]GGCTCCGCCGCCCCG	84132
rs775321779	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6084322	GTGAGCCACCACACC[C/G]AGCCCTGAAGAGGGT	84132
rs775351583	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098373	CCTTGATCTAGGCCC[C/T]GTAGTATCCATTCCC	84132
rs775382885	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6119051	AGACCCTGTCTCTCC[-/A]AAAAAAAAAAAAAAT	84132
rs775396125	in-del	-/AA			utr-variant-3-prime, intron-variant, downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6162059	ACCTAACTTCTCAGC[-/AA]AAAGCATATCTATGT	84132
rs775398011	snp	C/T	3.55151e-05	0.00421382	synonymous-codon	USP42	GRCh38.p7	7:6154947	CCCGCACCCCGACCG[C/T]TTCTCCCACGACAGA	84132
rs775409280	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6100491	CTTGCAACCATGCCC[A/G]GCTAATTTTTGTATT	84132
rs775417741	snp	A/G	1.65611e-05	0.00287755	missense	USP42	GRCh38.p7	7:6145543	CCTGAGTATCTTGAT[A/G]TTCGGCCATATATGT	84132
rs775420268	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6141488	GGCGTGAGCCACCGC[A/G]CCCGGCCTGAATTTT	84132
rs775470672	snp	A/G	1.65833e-05	0.00287948	intron-variant	USP42	GRCh38.p7	7:6159400	ACAGCAGAGGCCCTG[A/G]CGATTTTGCAACCAT	84132
rs775537415	snp	A/G	1.75912e-05	0.00296569	intron-variant	USP42	GRCh38.p7	7:6149549	GTGACCATGTTTCTG[A/G]AGCTCTGACCAGGTG	84132
rs775543271	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6135028	CTCTTGGCCCCAAGA[C/G]ATGCACCCACCTCAG	84132
rs775545375	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6124648	TTTATTTTGAGGCAT[C/T]ATACCTTTTACATTT	84132
rs775585294	snp	C/G	1.76658e-05	0.00297197	missense	USP42	GRCh38.p7	7:6154458	GGAGCCCGCCAGAGA[C/G]AGCAGGAGCAAGACT	84132
rs775587133	in-del	-/CTGT	0.000116048	0.00761646	intron-variant	USP42	GRCh38.p7	7:6159507	TGGTAAGCTGTTTTC[-/CTGT]CTGTTTCCTCATTGT	84132
rs775639978	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6136809	TTTTTTCGGTTCTTC[-/T]TTTTTTTTTTTTTCA	84132
rs775649648	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6119848	AGCCAGGACTACAGG[A/C]ATGTGCTACAACACC	84132
rs775652534	snp	C/T	1.65605e-05	0.0028775	missense	USP42	GRCh38.p7	7:6149680	TCAACAGGGCTAGTC[C/T]TGTTAATGCTTCAGC	84132
rs775681856	snp	C/T			utr-variant-5-prime	USP42	GRCh38.p7	7:6084575	CTCCACATCGCTGCC[C/T]GCATCACCACGCTGC	84132
rs775689976	snp	G/T	3.03679e-05	0.00389654	intron-variant	USP42	GRCh38.p7	7:6135793	TAGCCTTGATGTGTG[G/T]ATATGGTTGTATTTT	84132
rs775707566	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6140331	TCATTCCTTTTACCC[-/A]GAGGCAGCCTCGGTG	84132
rs775745998	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6117799	ACTTTCATAATGAAT[A/G]ATGCTGAACCTCTTT	84132
rs775758853	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6128593	TCTGTGTCTTTTAAC[A/T]CTCTGCTGCTCTAGG	84132
rs775767964	snp	A/T	1.65704e-05	0.00287836	missense	USP42	GRCh38.p7	7:6150497	TGAAAGGCTCGACGG[A/T]TGAAATGAGGTAACG	84132
rs775777004	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6152736	TTCATTATTAACCCC[A/G]AGGATATATCGAAAG	84132
rs775778721	snp	C/T	0.000257942	0.0113536	synonymous-codon	USP42	GRCh38.p7	7:6154389	GAAAATCGGCAGCCT[C/T]AGAAAGGTGGACCGA	84132
rs775821600	snp	A/G	6.53552e-05	0.00571606	intron-variant	USP42	GRCh38.p7	7:6144241	TATGTCGAGCCTTTC[A/G]AAGCTTAACGTGTCT	84132
rs775847261	snp	C/G	3.34756e-05	0.00409105	intron-variant	USP42	GRCh38.p7	7:6155219	GGGGCCTTGTGCTCC[C/G]CGAGGCGCTGGCGCT	84132
rs775853943	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6094314	TAGTAGCTGGGACTA[C/T]AGGCATGCACCAGCA	84132
rs775888166	snp	C/T	1.67105e-05	0.0028905	synonymous-codon	USP42	GRCh38.p7	7:6149945	AACAAAACCGATCCC[C/T]CGCAGTGAATCCTGC	84132
rs775947852	snp	C/T	1.81526e-05	0.00301264	missense	USP42	GRCh38.p7	7:6154130	GGTTGAGTCCGGCTC[C/T]GCCTGCGCGGTCGGA	84132
rs775948613	snp	A/G	2.05835e-05	0.00320801	intron-variant	USP42	GRCh38.p7	7:6111397	TTTTCAAAAGAGAGA[A/G]TTACCGCCAGAAACT	84132
rs775966268	snp	A/C/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6080092	GCCAGGCCTGGTGGC[A/C/G]GACGCCTGTAGTCCC	84132
rs776002212	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6089751	TTGGTCAGGCTGTTC[A/T]CAAACTCCTGACCTC	84132
rs776028494	snp	A/G	1.7673e-05	0.00297257	missense	USP42	GRCh38.p7	7:6149995	GCAAATCCAAGCTGA[A/G]CTCCAGCGTGCTGGT	84132
rs776037919	snp	A/G	3.31296e-05	0.00406985	synonymous-codon	USP42	GRCh38.p7	7:6150441	TTTGCTGTCTCTCCC[A/G]GAAGACAAAATCTTA	84132
rs776038053	snp	C/T	1.8335e-05	0.00302773	missense	USP42	GRCh38.p7	7:6154165	CCCTGCGAGCAGCCA[C/T]TCCTTGTTCACCCCA	84132
rs776045315	snp	C/G	3.57187e-05	0.00422588	missense	USP42	GRCh38.p7	7:6155113	GAACAGAAGGATCCT[C/G]TAGAAGAGCCTAAAG	84132
rs776057158	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114280	AATGAATTAGCATCC[A/G]TGGCAGATGTTACAA	84132
rs776074123	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6106208	AGTTTAAGGCCAGTC[G/T]TTTGGTTTACTTAAG	84132
rs776074142	in-del	-/TTTATTTATTTT			intron-variant	USP42	GRCh38.p7	7:6083263	TTATTTATTTATTTA[-/TTTATTTATTTT]AGATACAGTCTAGCG	84132
rs776095761	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6144982	AAAATAATAAATGCA[A/G]CAGGATGGCCTTAAA	84132
rs776101948	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6078952	GGGCATATCCCTTTT[C/G]GTTTTAAAGCCTCCA	84132
rs776124363	snp	C/T	5.53123e-05	0.00525862	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111171	CTGAATCTTCAGACC[C/T]ATCAGCCTATCAGAA	84132
rs776140543	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6138270	TGTAATTTAAAAAAT[A/C]ATTTGGTCTTTTAGC	84132
rs776142223	in-del	-/AA	1.67511e-05	0.00289401	intron-variant	USP42	GRCh38.p7	7:6156711	TCTGCTGCTGGTGGT[-/AA]TTTGTGTTTTAGGGT	84132
rs776145860	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6120893	CCGGCTGGAATAAAT[A/G]TTTTCATTAACTATT	84132
rs776147745	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6110586	TGGTTTTAAAGGTGA[C/G]ATCTCTATAATTATA	84132
rs776166513	snp	C/T	1.67119e-05	0.00289062	missense	USP42	GRCh38.p7	7:6156912	CCAGCTTGGAGACTG[C/T]CGCCCAGTTCCGGAG	84132
rs776176715	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6157658	TTGATAGAAATACTT[C/T]TGCAGCGTATACGTT	84132
rs776198502	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6106144	GGGTCAGTTTCACTT[A/T]CTCTTCTGTATCTTT	84132
rs776204730	snp	G/T	1.65605e-05	0.0028775	missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115379	CCATCTGAGAAGATT[G/T]GTCTTAAGTGGCAAC	84132
rs776300073	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6146982	CCCGCACCCAGCTCT[A/G]TCCTGTTGTGGCTGC	84132
rs776314695	snp	C/T	1.65888e-05	0.00287996	synonymous-codon	USP42	GRCh38.p7	7:6142997	GCTTGATGGAGAAAA[C/T]TCGTACAAGTGCAGC	84132
rs776321704	snp	C/T	1.6964e-05	0.00291233	intron-variant	USP42	GRCh38.p7	7:6142897	ACAAGTGACGGTGTG[C/T]GGTGATGTGGTGTTT	84132
rs776322779	snp	G/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6104536	ACTCCTGCGTCCCCA[G/T]GTGCCCCGCTTCTGG	84132
rs776334152	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6136412	CTTTGATAACAAATT[G/T]TTAGTAAAACATTTG	84132
rs776354202	snp	C/T	1.6582e-05	0.00287936	synonymous-codon	USP42	GRCh38.p7	7:6147859	GGCTGCGCCAGGCTT[C/T]ATCGGACCACAGCTT	84132
rs776363623	in-del	-/T/TT			intron-variant	USP42	GRCh38.p7	7:6099211	CCATTGTTCCCTCTC[-/T/TT]TTTTTTTTTTTTTTT	84132
rs776377435	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6084423	ATGTTTTCATTTTTG[C/T]CCTAGGAGGCTTGAC	84132
rs776392418	snp	A/C	4.44444e-05	0.00471384	missense	USP42	GRCh38.p7	7:6153817	CCTCAGCCTGGCAGC[A/C]CCGCCGCCGAATCCC	84132
rs776392661	snp	C/T			utr-variant-3-prime	USP42	GRCh38.p7	7:6161255	TGATACTGGAGTCTC[C/T]GTTGTCTGCTTGGTC	84132
rs776394362	snp	A/T	3.64664e-05	0.00426988	missense	USP42	GRCh38.p7	7:6154270	GCTCCTGTGCTGGAC[A/T]TGGCCCCGGCCGGTC	84132
rs776432130	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6101264	CTGGGTGGGGCATTA[A/G]CAGTGCCCACTGCAG	84132
rs776464473	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6096397	TGGGTGCATCATTGC[A/C]TGGAGAGGAGGGATC	84132
rs776488057	snp	A/G	1.79858e-05	0.00299876	missense	USP42	GRCh38.p7	7:6153865	GCCGCCGGCCTCAGC[A/G]GCACCAAGAAGGCTC	84132
rs776499410	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6096897	CCAGTCTCTGACACT[A/C]CAGGATGCCATCATT	84132
rs776515912	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151072	CTGTAATACAGTGGT[A/G]TTTGTGTATCTAAAC	84132
rs776528056	snp	A/G	3.40913e-05	0.0041285	synonymous-codon	USP42	GRCh38.p7	7:6150167	AGAACCCATGACCCT[A/G]AACGGTGCTAATAGT	84132
rs776564150	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6131912	TTGAATGATATTCTC[A/T]TGGGGTGTAGAATTC	84132
rs776575394	snp	C/T	1.73788e-05	0.00294772	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116817	TTCATTCCCCACAGA[C/T]AGCTTTCCTATCACT	84132
rs776592351	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6123259	CTGGGCATGATGGCT[C/T]ATGCCTGTAATCCCA	84132
rs776593055	in-del	-/ATCA			intron-variant	USP42	GRCh38.p7	7:6121974	CTCCTTTTTCGTTTG[-/ATCA]ATCTGACCAGAAGTT	84132
rs776612818	snp	A/G	3.53826e-05	0.00420595	missense	USP42	GRCh38.p7	7:6154027	GATCCCGGGAGCTTA[A/G]CAGGCGATGCGAGCC	84132
rs776618352	snp	A/G			utr-variant-3-prime	USP42	GRCh38.p7	7:6160764	CCATTGTAAAATACC[A/G]TGTATATAAATCCCA	84132
rs776633264	snp	A/C	6.43004e-05	0.00566975	missense	USP42	GRCh38.p7	7:6154839	GCGGCCGCACAAGGA[A/C]CACAACCGGGGCCGT	84132
rs776633485	snp	C/T			intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153237	GAGATCACACCACTG[C/T]GCTCCAGCCTGGGCA	84132
rs776640743	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6159058	GTCCTTCTGAGAAGG[C/T]CGCTGCCCGGCCCCG	84132
rs776701056	snp	C/T	1.67683e-05	0.00289549	synonymous-codon	USP42	GRCh38.p7	7:6150233	AGCGCCTGATGGTGC[C/T]AGCTGCCAAGGCCAG	84132
rs776727180	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6132835	TGCCACCACACCCGG[C/T]TAATTTTTTTGTATT	84132
rs776732844	snp	A/G	7.87867e-05	0.00627592	synonymous-codon	USP42	GRCh38.p7	7:6155094	AAAGAAAGCCCGGAG[A/G]AGCGAACAGAAGGAT	84132
rs776769123	in-del	-/CTAG			intron-variant	USP42	GRCh38.p7	7:6102786	TGGAGTTTCTGATAC[-/CTAG]CTAAGGAATTTAGAC	84132
rs776775138	snp	C/T	8.53916e-05	0.00653365	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111263	GGTGCTGTGTCTTCA[C/T]TGAATGATGTGTCAA	84132
rs776783556	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6119386	TGAGGTGAGAGGCTC[A/G]CTTCAGCTCAGGAGG	84132
rs776794887	snp	C/T	1.65627e-05	0.00287769	missense	USP42	GRCh38.p7	7:6149761	CTAAGAAACAAAAAA[C/T]TACAATCAGTATTCA	84132
rs776822625	snp	A/G	3.878e-05	0.00440324	intron-variant	USP42	GRCh38.p7	7:6150340	AGCCTCGTTTGTGGC[A/G]GTTCCCTTGGCTGGA	84132
rs776851909	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6108512	TTAAAGACAGAGTCT[C/T]GCTCTGTCGCCAGGC	84132
rs776874912	snp	C/T			utr-variant-5-prime	USP42	GRCh38.p7	7:6088873	ACCCGCAGGAGGGGA[C/T]GGCGGGAACCAAGAT	84132
rs776889941	snp	A/T	1.65756e-05	0.00287881	missense	USP42	GRCh38.p7	7:6150412	TTGTTTTTATTGCAG[A/T]TGATGCCTGCTCCTT	84132
rs776924522	snp	A/G	8.03632e-05	0.00633839	missense	USP42	GRCh38.p7	7:6154333	GAGAGGGTCGAGGAC[A/G]CCGCGGCGCCGAAAG	84132
rs776942685	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6151722	GGCTGGGATTCCAGA[C/G]GTGAGCCACCGTGCC	84132
rs776967223	in-del	-/TC	1.65921e-05	0.00288024	frameshift-variant	USP42	GRCh38.p7	7:6142944	AGGCTGCTCAGAGTG[-/TC]TCAACAAGGCATTGG	84132
rs777003330	in-del	-/G			intron-variant	USP42	GRCh38.p7	7:6147083	CTCAAATGTCCAACT[-/G]GCAGAATGCTCATGT	84132
rs777009017	snp	A/G	1.81929e-05	0.00301598	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111152	ACCATAGTTGACAAA[A/G]CTTCTGAATCTTCAG	84132
rs777016423	snp	C/G	1.81043e-05	0.00300862	synonymous-codon	USP42	GRCh38.p7	7:6154125	GGAAGGGTTGAGTCC[C/G]GCTCCGCCTGCGCGG	84132
rs777017627	snp	A/G	1.77941e-05	0.00298274	synonymous-codon	USP42	GRCh38.p7	7:6154092	GGGCCCGCGGGACTC[A/G]GCGTTGGCGGAAGCC	84132
rs777030709	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6121801	TCCTGAGTAGCTAGA[G/T]GTGTGCATCACCACA	84132
rs777071468	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6139684	TTGGTGCTGTCTGAG[-/A]CACCTGGTAGATCTC	84132
rs777117298	snp	A/C	4.53278e-05	0.00476045	synonymous-codon	USP42	GRCh38.p7	7:6154621	AGTCACCACCACTCC[A/C]GACACCGGAGCGGGG	84132
rs777134190	snp	A/T	1.69527e-05	0.00291137	intron-variant	USP42	GRCh38.p7	7:6147911	ACAGTCCTTAGGGAG[A/T]AGAACATTTTTATGT	84132
rs777135355	snp	C/T	2.69771e-05	0.00367258	missense	USP42	GRCh38.p7	7:6154678	TACACCGAGGGCGAG[C/T]GTGGCTGGGGCCGGG	84132
rs777176853	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6088029	TCTAGGACAGGCATG[A/G]TGGCTCATACCTGTA	84132
rs777186678	snp	C/T	4.53196e-05	0.00476002	intron-variant	USP42	GRCh38.p7	7:6139076	ATAAAGCCTTGTCTT[C/T]ACCGAAATTTTACAG	84132
rs777189772	snp	C/G	7.21098e-05	0.00600414	missense	USP42	GRCh38.p7	7:6154944	CGCCCCGCACCCCGA[C/G]CGCTTCTCCCACGAC	84132
rs777212225	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6101373	TCGGACTTGAGGGTG[A/G]GGCACTTGGAATCAG	84132
rs777220314	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6085074	CTGGCATGAACGACT[A/G]TGCCCAGCCTTGTTT	84132
rs777234333	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6129560	AGGCTCTGCCTCAGG[-/A]AAAAAAAAAAAAAAA	84132
rs777296055	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6146985	GCACCCAGCTCTGTC[C/T]TGTTGTGGCTGCATA	84132
rs777362239	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6141784	TTTTTCTGATTACAG[A/G]TGTAATACATGCTTA	84132
rs777362385	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6130620	CCAGTATGGGTTAGG[G/T]TGCCTTGCTACAGCC	84132
rs777378198	snp	G/T	6.89227e-05	0.00586998	missense	USP42	GRCh38.p7	7:6154267	CCAGCTCCTGTGCTG[G/T]ACATGGCCCCGGCCG	84132
rs777384519	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6120581	TTGGGATTTCAGGCA[A/T]GAGCCACTATGCCTG	84132
rs777386229	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6117579	GTAAAATGGCTTGGT[C/G]CTGGGGTGGGTGTGT	84132
rs777386327	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6125841	TTTTTGGTTTGAAAT[G/T]TCTTTATTTTGCTTT	84132
rs777399942	snp	A/G	1.77357e-05	0.00297784	missense	USP42	GRCh38.p7	7:6135879	ATGTGTACAATGCAA[A/G]CACATATTACCCAGG	84132
rs777413676	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6108088	ACCCTGGAGGCTGAG[A/G]CAAGAGAATCACTTG	84132
rs777466509	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6144763	TAATCCTAGCTACTC[A/G]GGAGGCTGAGGCAGG	84132
rs777516979	in-del	-/TATTTATT			intron-variant	USP42	GRCh38.p7	7:6089024	GGGGTTTCTTTTCTA[-/TATTTATT]TATTTATTTATTTAT	84132
rs777540152	snp	C/G	2.34761e-05	0.003426	missense	USP42	GRCh38.p7	7:6156755	TTTTCCTTCTGCAGG[C/G]ATCAGCAGGACTCAG	84132
rs777570284	snp	A/G	1.76649e-05	0.00297189	missense	USP42	GRCh38.p7	7:6154061	TGTCCCAGGACGCAA[A/G]GGGGATGATCGCGGA	84132
rs777580233	snp	G/T	2.03884e-05	0.00319277	missense	USP42	GRCh38.p7	7:6154924	GCAGGCGCGCCCCAC[G/T]CCCTCGCCCCGCACC	84132
rs777622040	snp	A/G	3.31323e-05	0.00407002	missense	USP42	GRCh38.p7	7:6149887	CCAATTCTGCAGTAC[A/G]GTCTACCTCGAACGC	84132
rs777622817	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6118227	AGGGAGAACTCATCT[C/G]TATATATAAAAAAAA	84132
rs777625663	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6101126	GCAACAATATTGTCT[C/G]AGTGGGAGATGAGTC	84132
rs777627869	in-del	-/TTTG			intron-variant	USP42	GRCh38.p7	7:6119708	TGTTGTTGTTGTTGT[-/TTTG]TTTTTTTTTAGTGAC	84132
rs777628015	snp	G/T	0.000178428	0.00944363	missense	USP42	GRCh38.p7	7:6154528	GAGCGCGACCGCCAG[G/T]ACCGCCACGCCCCGG	84132
rs777693276	in-del	-/AT	1.66161e-05	0.00288232	intron-variant	USP42	GRCh38.p7	7:6140234	TAAAATGATACACAC[-/AT]GTGGTTAAAAAATGG	84132
rs777706556	snp	A/C	1.99834e-05	0.0031609	intron-variant	USP42	GRCh38.p7	7:6145660	TGCTACATAAAAGTA[A/C]GCTGTGCAGATTTGC	84132
rs777714915	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6079381	GAGAATCGCTTGAAC[C/G]CCGGAGGCGGAGCTT	84132
rs777732022	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6100225	ATAAGCCAACACATC[C/G]CCTTCTACTCATATC	84132
rs777736697	snp	C/T	0.000110029	0.00741637	synonymous-codon	USP42	GRCh38.p7	7:6154452	CAGCGGGGAGCCCGC[C/T]AGAGAGAGCAGGAGC	84132
rs777748301	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6083894	CTAGCAAGGATAGAT[A/T]TGTACTGATCCCTAA	84132
rs777748784	in-del	-/TGTAA			intron-variant	USP42	GRCh38.p7	7:6090969	TGTTAGGGATCAATT[-/TGTAA]TCATCACAGTTACAA	84132
rs777757125	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6086892	CACCATACCTGGCTA[A/C]ATTTTTTGTATTTTT	84132
rs777766601	snp	G/T			downstream-variant-500B	CYTH3, USP42	GRCh38.p7	7:6161756	CAACAATATCTGTTT[G/T]AAAGAACCAAGTCTT	84132
rs777797383	snp	A/T	1.67164e-05	0.00289101	intron-variant	USP42	GRCh38.p7	7:6140072	TTGAAATCTGGTCAC[A/T]GCATCTGGAGTTTTT	84132
rs777836548	snp	A/G	2.60542e-05	0.00360921	missense	USP42	GRCh38.p7	7:6154664	GGGTCAGACACCACT[A/G]CACCGAGGGCGAGCG	84132
rs777852271	snp	A/G	1.65971e-05	0.00288067	intron-variant	USP42	GRCh38.p7	7:6140223	TTATAAGTTGATAAA[A/G]TGATACACACATGTG	84132
rs777907211	snp	A/G	1.65627e-05	0.00287769	synonymous-codon	USP42	GRCh38.p7	7:6145524	CTTCTAGGATGTGAA[A/G]TACCCTGAGTATCTT	84132
rs777922887	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6129048	AACTCCTGGGCTCAG[A/G]CCATCCGCCCACCTC	84132
rs777927824	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6105634	TGGAGAGTCCGAGGT[A/G]CCCACGCCGGGCGGA	84132
rs777930136	snp	G/T	2.06943e-05	0.00321663	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6111234	GAGACATGGATGCAG[G/T]TTCTGCCAGCTGGGG	84132
rs777939925	snp	C/T	1.66651e-05	0.00288657	intron-variant	USP42	GRCh38.p7	7:6150387	GCTGGCGACTGAAGC[C/T]GAAATATTTTTGTTT	84132
rs777943303	snp	A/G	6.69434e-05	0.00578508	missense	USP42	GRCh38.p7	7:6153913	GGCACCCCCGCTACC[A/G]AAGAAGGCGCCTGGG	84132
rs777947561	snp	A/C/G	0.000867654	0.0208107	missense	USP42	GRCh38.p7	7:6154205	ACGCCCGGGACGCTC[A/C/G]GGACCCATCCCAGAG	84132
rs777995061	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148566	TTAGTCGTTTCAGGG[A/G]TGTGGTGTTTCTGTC	84132
rs777996474	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6157556	GCGCCCGCCACCACG[C/G]CCGGCTAAATTTTGT	84132
rs778019205	snp	C/T	1.78867e-05	0.00299049	intron-variant	USP42	GRCh38.p7	7:6147712	GGTGTCCTGTGTCAC[C/T]CTAAGTATCGCTCTC	84132
rs778072339	snp	C/T	1.71985e-05	0.0029324	synonymous-codon	USP42	GRCh38.p7	7:6156973	CCCGCCTCTGGAAGG[C/T]GTCGGACCTTTCCGT	84132
rs778073908	snp	C/T			missense	USP42	GRCh38.p7	7:6149902	AGTCTACCTCGAACG[C/T]ATCTACGATGTCAGT	84132
rs778078085	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6122970	CTGGGATTACAGGCA[A/T]GCGCCACCACACCTG	84132
rs778126815	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6078374	TTGGGAGGCTGAGGC[A/G]GGCAGATCATTAGGT	84132
rs778144846	snp	C/T	1.71941e-05	0.00293202	synonymous-codon	USP42	GRCh38.p7	7:6149978	CCAGCCCGTGATGAA[C/T]GGCAAATCCAAGCTG	84132
rs778196776	snp	A/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115138	TACTGGAGAAACCAG[A/G]TCATTGAAAATTTCT	84132
rs778226678	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6084181	ACAGGCATGAGCCAC[C/T]ACGCCCAGCTAATTT	84132
rs778230149	snp	C/T	3.34947e-05	0.00409221	synonymous-codon	USP42	GRCh38.p7	7:6150215	CCCGAAAGAAAACGG[C/T]CTAGCGCCTGATGGT	84132
rs778248650	snp	C/G	0.000332226	0.0128842	missense	USP42	GRCh38.p7	7:6154803	CGGCGGCCGCGAGCA[C/G]GAGCGGGCCGGGCTG	84132
rs778258744	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6124036	ATGCGCCGCCGTGCC[C/T]GGCTAACTTTTGTAT	84132
rs778260480	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6119085	CTGCATCTGGGAACT[C/G]ATGCCTATAGTCCTA	84132
rs778266356	snp	C/G	1.66693e-05	0.00288693	missense	USP42	GRCh38.p7	7:6156888	CAGAACTGCACTTAC[C/G]CAGGGTCACCAGCTT	84132
rs778272839	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6142070	TGGATATTTGGTTTG[C/T]TTCCAGTTTTATGTA	84132
rs778277950	snp	A/C	1.738e-05	0.00294783	intron-variant	USP42	GRCh38.p7	7:6116765	GCCAGAATTAACGTT[A/C]TGTTTGCCCTCATTT	84132
rs778281173	snp	A/G	5.65579e-05	0.00531749	intron-variant	USP42	GRCh38.p7	7:6135965	GCGTAAGTATTAACT[A/G]TTGTAGTTTTATATT	84132
rs778287900	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6105572	CAGAGGCAAAGTTTT[-/C]CCACCTTGGGCGCCC	84132
rs778288369	snp	C/T			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079878	GTAGAGAAGATACAG[C/T]ATGTATATATACATT	84132
rs778294038	snp	G/T	3.15871e-05	0.00397398	intron-variant	USP42	GRCh38.p7	7:6144036	CAAAATACCACAAAT[G/T]GTGTGTATATATTCG	84132
rs778309800	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6146337	AATATTCAGTGTTTT[-/A]AAAAAAAAAAAAAAA	84132
rs778310717	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6098057	TTACAGGCACACACC[A/T]CTACCCCACAGCTAA	84132
rs778342108	snp	A/T			upstream-variant-2KB	USP42	GRCh38.p7	7:6077113	CTCCTGATCTTGTGA[A/T]CTGCCCACCTCAGCC	84132
rs778382578	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6138853	CCCCTCTTCTGGTCT[G/T]TGGAAAAATGGTCTT	84132
rs778404610	snp	C/T	5.61561e-05	0.00529858	missense	USP42	GRCh38.p7	7:6154306	GAAGGGGACGCTGAG[C/T]CTAGCCCCGGCGAGA	84132
rs778410210	in-del	-/AGCCCCAGGCCC	1.69896e-05	0.00291454	cds-indel	USP42	GRCh38.p7	7:6154346	CGCCGCGGCGCCGAA[-/AGCCCCAGGCCC]AGCCCCAGGCCCTTC	84132
rs778412277	snp	A/G	6.97995e-05	0.00590719	synonymous-codon	USP42	GRCh38.p7	7:6153885	CAAGAAGGCTCCGCC[A/G]CCCCGCGATCCCGGC	84132
rs778439591	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148648	CAGTAGTGAGCTAGT[A/G]TCACAAGGAACACAG	84132
rs778515548	snp	C/G	6.41265e-05	0.00566208	missense	USP42	GRCh38.p7	7:6154519	TGCCCCCGGGAGCGC[C/G]ACCGCCAGGACCGCC	84132
rs778550844	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6086180	ACCTGGGATTACAGG[A/C]GCCTGCCACCTCACC	84132
rs778560975	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6140831	AAATTTTAAATTTCA[A/T]AATTGTATTTTGTCA	84132
rs778563184	snp	A/G	2.29434e-05	0.00338691	intron-variant	USP42	GRCh38.p7	7:6144213	TATGTGGATGATGTC[A/G]TTAATCATGTTTTAT	84132
rs778567698	snp	A/G	1.88759e-05	0.00307207	missense, utr-variant-5-prime	USP42	GRCh38.p7	7:6135850	TTTCAGGTCATGCAG[A/G]AGGCTTTTGTATGAT	84132
rs778577940	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6132534	AGGTAATTTTTTGGA[C/T]TTTTAGTAGAGACAG	84132
rs778591913	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6101167	CTAAGAACAGCCTCA[A/G]GAGAAGAGGCAGCTG	84132
rs778593373	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6145449	GAAGCTCTAAGTACC[-/CT]CTACCTGAATATGTG	84132
rs778601962	snp	G/T	5.2158e-05	0.0051065	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116898	GGACAGCAAGAGAGA[G/T]GACCAAGACAAAATT	84132
rs778603846	snp	C/T	3.54704e-05	0.00421117	missense	USP42	GRCh38.p7	7:6154016	CTGACCTGTGTGATC[C/T]CGGGAGCTTAACAGG	84132
rs778609131	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6151524	CTCACTGCAGCCTCC[A/G]CCTCCCAAGTTCAAG	84132
rs778611775	snp	A/G	0.00010313	0.00718014	missense	USP42	GRCh38.p7	7:6154441	GAGCGCTCGTCCAGC[A/G]GGGAGCCCGCCAGAG	84132
rs778631377	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6143143	TGGGAAGACACTGCG[G/T]CCCTGTCGTCCAAAG	84132
rs778646966	snp	A/G	2.0423e-05	0.00319548	synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111361	ATCAAAACCATCACC[A/G]CAAAAGGATCAAGGT	84132
rs778648143	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096681	ATCCCTGGAGATTAA[C/T]CCCAAGTTCCTATAA	84132
rs778663543	in-del	-/CG			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081542	GACCCGCCCCACCCA[-/CG]CGCGCGCCGCAGTTT	84132
rs778665692	snp	C/T	1.75804e-05	0.00296478	missense	USP42	GRCh38.p7	7:6150148	CCACTCCGCACGAGC[C/T]TCAAGAACCCATGAC	84132
rs778666989	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6136453	ACATTTTGAAACTTT[A/T]AAGCAAAAGATGACA	84132
rs778667661	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126886	TCTGGGATAAATGCC[C/T]AGGACTGCAAATGCT	84132
rs778699862	snp	A/G	1.81876e-05	0.00301554	synonymous-codon	USP42	GRCh38.p7	7:6153975	GCCCAGCGCCGGCGA[A/G]GACATCGTGGGGGAC	84132
rs778721875	in-del	-/C					GRCh38.p7	7:6087044	CACACTTTTTTTTTT[-/C]CTTTTGAGACAGAGT	84132
rs778725705	snp	C/G	1.65743e-05	0.00287869			GRCh38.p7	7:6159467	GATTGAAAACTCAGC[C/G]TCAAAACAAAAAATT	84132
rs778773872	snp	C/G	0.000113578	0.007535	missense	USP42	GRCh38.p7	7:6155179	TCCAAAGACAAACAC[C/G]GAGACCGCGACTCCA	84132
rs778793463	snp	A/G	1.72445e-05	0.00293632	missense	USP42	GRCh38.p7	7:6155084	GTCATGTTGAAAAGA[A/G]AGCCCGGAGGAGCGA	84132
rs778809784	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6089714	ATTTTTTTGTATTTA[C/G]TAGAGATGGGGTTTC	84132
rs778842041	snp	A/G	1.65633e-05	0.00287774	missense	USP42	GRCh38.p7	7:6149821	CTCAACCTAACCTTC[A/G]TAGTAATTCTTTGGA	84132
rs778845688	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6143653	TCCACAGACATTTCT[A/C]ATATTTATTTTTATT	84132
rs778947632	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6112988	GGCTCACTGCAATCT[C/G]TGCCTGCTGGGTTCA	84132
rs778973343	snp	G/T	1.79861e-05	0.00299879	intron-variant	USP42	GRCh38.p7	7:6147698	ATCTCTCCTAAGGAG[G/T]TGTCCTGTGTCACCC	84132
rs778976025	snp	C/T	1.67652e-05	0.00289522	missense	USP42	GRCh38.p7	7:6156861	GAAAATCAGAGGACT[C/T]TGTTAAAGATTCAGA	84132
rs778996499	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	USP42	GRCh38.p7	7:6081168	TCTTTCAGATCAGAG[C/T]AACTCTGAGTCTGGT	84132
rs779034210	snp	A/G	1.65912e-05	0.00288016	intron-variant	USP42	GRCh38.p7	7:6150531	GAGTACATCTGAGGC[A/G]CGTGTGGCAGCATAG	84132
rs779036447	snp	A/C	1.65611e-05	0.00287755	missense	USP42	GRCh38.p7	7:6149745	GTGATCCCAGAACAT[A/C]CTAAGAAACAAAAAA	84132
rs779042117	snp	A/G	0.000310382	0.0124537	synonymous-codon	USP42	GRCh38.p7	7:6146171	TGGCCTCTGGTATCA[A/G]ATGAATGACTCCATT	84132
rs779049592	snp	G/T	4.2778e-05	0.00462463	intron-variant	USP42	GRCh38.p7	7:6145673	TAAGCTGTGCAGATT[G/T]GCTATTAACTATTGT	84132
rs779067574	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6146728	AGGTAGTGTCTGAGC[A/G]GGATGATGAGTTTGC	84132
rs779076715	snp	C/T	7.50694e-05	0.0061261	intron-variant	USP42	GRCh38.p7	7:6139210	GTAAGTACAACAGAG[C/T]GCCAGCCATGTCTTC	84132
rs779078931	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6095111	CTTTCTGTGCTACAA[G/T]AGCTCTTAATGCTGT	84132
rs779088668	snp	A/G	5.07215e-05	0.00503569	missense	USP42	GRCh38.p7	7:6154295	CCGGTCACCCGGAAG[A/G]GGACGCTGAGCCTAG	84132
rs779114040	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6130416	AGTGATGGTGACAGT[C/T]CTGCCTCTGACCCTC	84132
rs779116234	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120803	TGGCCAAGCTGGTCT[C/T]GAACTCCTGGCCTCA	84132
rs779174997	snp	A/C/T	6.13652e-05	0.00553891	missense	USP42	GRCh38.p7	7:6153883	ACCAAGAAGGCTCCG[A/C/T]CGCCCCGCGATCCCG	84132
rs779190626	snp	C/G	0.000148931	0.00862807	missense	USP42	GRCh38.p7	7:6153848	TGGAGGAGCCAGATG[C/G]GGCCGCCGGCCTCAG	84132
rs779219351	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6116293	GACTTTCCCTTTAGC[A/G]TTTGAGAACTTCATC	84132
rs779241379	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6079451	CGACAGAGCCAGACT[C/G]TGTCTCAAAAATAAA	84132
rs779253638	snp	C/T	5.09636e-05	0.00504769	synonymous-codon	USP42	GRCh38.p7	7:6156949	GGGTGGCTTTCCTCT[C/T]TCTGGTGGCCCGCCT	84132
rs779254186	in-del	-/AAAGC	0.000107043	0.00731507	intron-variant	USP42	GRCh38.p7	7:6139059	CTTATTACGTGTAAT[-/AAAGC]GATAAAGCCTTGTCT	84132
rs779301604	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6139772	TGACATACTTGGGTC[A/G]GAGGAAGACTCTCTG	84132
rs779361768	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137775	ACCTCCGCCTCTCGG[A/G]TTCCAGCGATTTCTC	84132
rs779379320	snp	A/G	2.32124e-05	0.00340671	intron-variant	USP42	GRCh38.p7	7:6157064	GGCCAGGGTAAGAGG[A/G]GATACTTGGAATTAG	84132
rs779387771	snp	C/T	1.65638e-05	0.00287778	missense, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115346	GATGGCATCGCTCCT[C/T]CACAGAAAGTTCTTT	84132
rs779417852	snp	A/C/T	0.00029853	0.0122139	missense	USP42	GRCh38.p7	7:6142948	CTGCTCAGAGTGTCA[A/C/T]CAAGGCATTGGAGCA	84132
rs779436653	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6140462	TTACATTTCAGCACA[C/T]AGGCCTAACAGCCTT	84132
rs779455010	snp	C/T	4.4403e-05	0.00471164	missense	USP42	GRCh38.p7	7:6154916	GCCCCCGCGCAGGCG[C/T]GCCCCACGCCCTCGC	84132
rs779456055	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6117386	TAGCATCACTTGATC[A/G]TATTGTTGAGTAGGA	84132
rs779463382	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6109817	GCGATTTTCCTGACT[C/T]AGCCTCCCAAGTAGT	84132
rs779503225	in-del	-/TTTC			intron-variant	USP42	GRCh38.p7	7:6096912	CCAGGATGCCATCAT[-/TTTC]TTTCTTTCTTTCTTT	84132
rs779523840	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6129212	GAGGGACGTATAGAA[A/C]CATTACTTCCCTATG	84132
rs779528308	snp	A/G	1.68772e-05	0.00290488	intron-variant	USP42	GRCh38.p7	7:6147905	AAGGTAACAGTCCTT[A/G]GGGAGAAGAACATTT	84132
rs779539683	snp	A/C	1.73794e-05	0.00294778	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116868	GGTGTGGATGAAAAC[A/C]CAGCACTAGCACCTG	84132
rs779558203	snp	C/G	2.33872e-05	0.00341951	intron-variant	USP42	GRCh38.p7	7:6135830	TTGGAGGATTATCAT[C/G]TATCTTTCAGGTCAT	84132
rs779568368	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6125907	GATTCACATGCACTT[A/G]TAAGAAATAATATAG	84132
rs779580359	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6123143	TTATGCCCTCTTGAT[C/G]AACTCATTTCGTTAC	84132
rs779616023	snp	C/T	3.52243e-05	0.00419653	intron-variant	USP42	GRCh38.p7	7:6141024	ATTACATTTTTAAAA[C/T]AAGTCATTTTATGTA	84132
rs779629704	snp	A/T	2.2505e-05	0.0033544	intron-variant	USP42	GRCh38.p7	7:6144208	TAAGGTATGTGGATG[A/T]TGTCATTAATCATGT	84132
rs779637362	snp	C/T	9.19075e-05	0.0067783	missense	USP42	GRCh38.p7	7:6154420	GGCCACTACCGCAGC[C/T]GGAGAGAGCGCTCGT	84132
rs779639409	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081373	CCGCCGCGGGGAGGT[A/C]GATGGCGGGCGGCGC	84132
rs779647689	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6102693	CTTTCTACAAGCAGA[G/T]GTAGTAGTGGGGTAG	84132
rs779693835	in-del	-/TA			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114598	GGTTGTTGTTTTATG[-/TA]TATATATAAAATATA	84132
rs779695905	in-del	-/CT			intron-variant	USP42	GRCh38.p7	7:6155784	AGAGACAGGGTGTTG[-/CT]CTGTCACCCAGGCTG	84132
rs779704029	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6157617	TAGCCAGGATGGTCT[C/T]GAGAACTCTTGGTTT	84132
rs779731292	snp	C/G	8.47925e-05	0.00651069	synonymous-codon	USP42	GRCh38.p7	7:6154362	AGCCCCAGGCCCTTC[C/G]CCAGCGAAGGAGAAA	84132
rs779742880	snp	C/G	1.79829e-05	0.00299852	synonymous-codon	USP42	GRCh38.p7	7:6150140	TGAGGAGGCCACTCC[C/G]CACGAGCTTCAAGAA	84132
rs779746286	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6090565	CCTAAAAATACAAAA[A/G]TTAGTTGGGCACGGT	84132
rs779751532	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6143202	TGTTTCTGCAAGATG[C/T]GCAGCTCTGTGCCTG	84132
rs779780818	in-del	-/ACTCCAGTTTTCTTTTTCGTATCGTTTCTCTTTTTT			intron-variant	USP42	GRCh38.p7	7:6123855	AAAAAAAAAAAAGCC[lengthTooLong]TTTGAGGTGGAGTCT	84132
rs779789478	snp	A/G	7.67018e-05	0.00619234	missense	USP42	GRCh38.p7	7:6155069	TGGAGAACAGTGACA[A/G]TCATGTTGAAAAGAA	84132
rs779793446	snp	C/T	1.80471e-05	0.00300387	intron-variant	USP42	GRCh38.p7	7:6140046	TTGATCTTTTGTGAG[C/T]TCCCATGTGTTTGAA	84132
rs779797255	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6143108	GTGTGTCTAGGTTGC[-/T]TTGAGTTTCTGATAC	84132
rs779799576	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6119988	TTTTGTTTTTTGAGA[C/T]GGAGTCTCGCTCTGC	84132
rs779806101	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6126921	TATATGGTAGTTGCA[C/T]ATTTGATTTTATAAG	84132
rs779819185	snp	A/C/G	0.00100273	0.0223692	missense	USP42	GRCh38.p7	7:6153931	GAAGGCGCCTGGGAG[A/C/G]CCATGGCCGTCGCCC	84132
rs779824399	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6123127	CACTGCACCTGGCCT[A/G]TTATGCCCTCTTGAT	84132
rs779825558	in-del	-/CTTTGACTGGACT	2.25996e-05	0.00336144	intron-variant	USP42	GRCh38.p7	7:6135996	GTATTTATTACCTAG[-/CTTTGACTGGACT]TTATACTTTTTTTTT	84132
rs779831321	snp	A/G			utr-variant-3-prime	USP42	GRCh38.p7	7:6160669	TGTACAGATTTTACC[A/G]TGGAGAACTTTTTTT	84132
rs779837296	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6085538	TATAGATTATATAGA[A/G]GAGGGACCTGCTGTA	84132
rs779884528	snp	C/T	3.31329e-05	0.00407005	synonymous-codon	USP42	GRCh38.p7	7:6150477	CTTCAGGCTTAGCAA[C/T]AAACTGAAAGGCTCG	84132
rs779892248	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098162	TCCACCTTGGCCTCC[C/T]AAAGTGCTGGGATTA	84132
rs779895611	snp	C/T	1.67632e-05	0.00289505	intron-variant	USP42	GRCh38.p7	7:6150381	CATGGAGCTGGCGAC[C/T]GAAGCTGAAATATTT	84132
rs779956506	in-del	-/TCT			intron-variant	USP42	GRCh38.p7	7:6092085	TCTTCCTCTTCCTCT[-/TCT]TCTTCTTCTTCCTCC	84132
rs779964249	snp	C/T			utr-variant-5-prime	USP42	GRCh38.p7	7:6084640	TACACCATTCGCCAT[C/T]GCACCTGGCTGTTTG	84132
rs780016153	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6131701	GGACTAGAAGAAGCA[C/G]AAAGAAACCCCAGGA	84132
rs780028152	in-del	-/AG			intron-variant	USP42	GRCh38.p7	7:6109656	ACTTTGGCCTCCCAA[-/AG]TGCTGGGATTACAGG	84132
rs780036808	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6127749	TTCGGCTATTCTAGT[G/T]ACATTGCTTTTCGTT	84132
rs780063619	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6083693	ACACACACACACACA[C/T]GCCCCCACAGGAAAT	84132
rs780076982	snp	C/T	1.65682e-05	0.00287817	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115336	AGCCCTAGGTGATGG[C/T]ATCGCTCCTCCACAG	84132
rs780078903	snp	A/T	1.90995e-05	0.0030902	intron-variant	USP42	GRCh38.p7	7:6111114	AAATACATACTTTTC[A/T]TCTTTTGCAGAGTTG	84132
rs780082260	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6102477	GAAATGGAAAATGAA[A/G]CTGGGTTGGTGTGGT	84132
rs780090200	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6091956	CTGGAAAAAATCCTA[C/T]TTAGTCCTCAAGGAC	84132
rs780106464	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6119264	ACTTTGTTCTTTCTC[C/T]GAGTTATGCTGTAGC	84132
rs780112274	snp	A/G			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6081279	AACGGAGGTGAGCTG[A/G]ACACACGTTCCCCAA	84132
rs780147251	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6133000	TCTCCAGTGCTTTTA[A/G]GATTTTTATCACTGG	84132
rs780149997	snp	C/T			synonymous-codon	USP42	GRCh38.p7	7:6147811	GTCCTCTCCCCGCCC[C/T]GTCATCAGTCAGCGG	84132
rs780153330	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6122280	TATGTCATGTGTCAG[G/T]TTTTTTTTTTTTTTT	84132
rs780162669	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6152316	TGGTGAAGTTCTGAT[C/G]AAATCACAGCATGAG	84132
rs780167853	snp	A/G	1.65734e-05	0.00287862	missense	USP42	GRCh38.p7	7:6149907	ACCTCGAACGCATCT[A/G]CGATGTCAGTTTCTA	84132
rs780172046	snp	C/G	3.31241e-05	0.00406952	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB	USP42	GRCh38.p7	7:6115438	GAATTTGGGCAATAC[C/G]TGTTTTGCCAATGCA	84132
rs780178302	snp	A/C	1.65638e-05	0.00287778	missense	USP42	GRCh38.p7	7:6149840	TAATTCTTTGGAGAA[A/C]CCTACCAAGCCCGTT	84132
rs780186021	snp	G/T	2.09317e-05	0.00323503	intron-variant	USP42	GRCh38.p7	7:6145669	AAAGTAAGCTGTGCA[G/T]ATTTGCTATTAACTA	84132
rs780211932	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6137422	GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTAC	84132
rs780230201	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6155689	TAGGCATCGGAGACA[A/C]CTTCGTTTCCTCGGC	84132
rs780238206	snp	G/T	1.98829e-05	0.00315294	missense	USP42	GRCh38.p7	7:6154537	CGCCAGGACCGCCAC[G/T]CCCCGGAGCACCACC	84132
rs780248338	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6110674	AAGTCTAGATTTTTT[C/T]TGTGTAGTTGATGCT	84132
rs780250618	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6113191	TAGGCCACTGCACCC[A/G]GACAACAGTAAGTTT	84132
rs780263670	in-del	-/TGGGTCAG			intron-variant	USP42	GRCh38.p7	7:6118628	TTTAGCTTTTGTTTT[-/TGGGTCAG]TGGTCCATTTTGAGT	84132
rs780271513	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6140644	TTCTGGATCACAGGG[A/C]GTGTGTATTGTAAAT	84132
rs780308224	snp	A/T	1.72246e-05	0.00293462	intron-variant	USP42	GRCh38.p7	7:6141007	TCATAATTATGGGAG[A/T]AATTACATTTTTAAA	84132
rs780327489	snp	C/T	3.75799e-05	0.00433457	synonymous-codon	USP42	GRCh38.p7	7:6154200	GGACCACGCCCGGGA[C/T]GCTCAGGACCCATCC	84132
rs780390047	snp	C/G	4.62332e-05	0.00480775	missense	USP42	GRCh38.p7	7:6154728	GCCGCGCTGGGACAG[C/G]TGCCGGTACTACCAT	84132
rs780417412	snp	A/G	1.66062e-05	0.00288146	intron-variant	USP42	GRCh38.p7	7:6150543	GGCACGTGTGGCAGC[A/G]TAGTAGGAAATCCAG	84132
rs780443872	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6097114	TGCTATCATCCTCTT[A/T]GCTACCAGACAGCCC	84132
rs780449792	snp	C/T	3.35999e-05	0.00409864	synonymous-codon	USP42	GRCh38.p7	7:6150191	TAATAGTGCAGACAG[C/T]GACAGTGACCCGAAA	84132
rs780479620	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6086268	TGGAGTGTAGTGGCG[C/T]GATCTCAGTTCACTG	84132
rs780481710	snp	C/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113920	GCCACTGTGCCCGAC[C/G]CAATCTCAGCCTTCT	84132
rs780504681	snp	C/T	0.000506842	0.0159111	missense	USP42	GRCh38.p7	7:6154358	CGAAAGCCCCAGGCC[C/T]TTCCCCAGCGAAGGA	84132
rs780511008	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6139825	TCCTCCCACACAGGC[C/T]GCAGTGCCCGGAGGC	84132
rs780564437	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6131362	TGCCTGTAATCCCAG[C/G]TACTCGAGAGACGGG	84132
rs780581028	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095262	CTTGATCCCTTAGCA[A/G]TAAGGGAACCCTGAG	84132
rs780582536	snp	C/T	1.65745e-05	0.00287871	intron-variant	USP42	GRCh38.p7	7:6159446	CCTGACCTTTGCTTT[C/T]TAGGTGATTGAAAAC	84132
rs780592254	snp	C/G	1.73785e-05	0.0029477	intron-variant	USP42	GRCh38.p7	7:6116773	TAACGTTCTGTTTGC[C/G]CTCATTTTCTCCCTT	84132
rs780642812	in-del	-/TGTC			utr-variant-3-prime	USP42	GRCh38.p7	7:6161012	GTCTGTTTTCTGTAA[-/TGTC]TGTCTGATACTAGAA	84132
rs780653528	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6091609	CTCATTCTCACCCCC[-/A]TATTAATTTTATTCT	84132
rs780659595	snp	C/G			intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6121580	TTGATGTTATTTCTT[C/G]TTTAAATGTTTGCTA	84132
rs780672578	snp	C/T			missense	USP42	GRCh38.p7	7:6154781	CCCGGGACTGGAAGC[C/T]CTTCCACGGCGGCCG	84132
rs780675102	snp	G/T	1.65798e-05	0.00287917	intron-variant	USP42	GRCh38.p7	7:6144046	CAAATTGTGTGTATA[G/T]ATTCGTCTTCTTATA	84132
rs780691695	snp	A/G	2.00226e-05	0.003164	synonymous-codon	USP42	GRCh38.p7	7:6144184	AAATTTTACCGGTGG[A/G]AAAATTGCTAAGGTA	84132
rs780762026	snp	A/C/G	0.000153483	0.00875913	missense	USP42	GRCh38.p7	7:6155065	AGTGTGGAGAACAGT[A/C/G]ACAGTCATGTTGAAA	84132
rs780765402	in-del	-/C			intron-variant	USP42	GRCh38.p7	7:6092017	CTTCTTCTTCTTCTT[-/C]TTCTTCTTCTTCTTC	84132
rs780786114	snp	C/G	4.42644e-05	0.00470428	missense	USP42	GRCh38.p7	7:6153892	GCTCCGCCGCCCCGC[C/G]ATCCCGGCACCCCCG	84132
rs780828977	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6124114	ATCTTAACCTCAGGT[C/T]ATCTGCCTGCCTCAG	84132
rs780838358	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6117504	TTAAGCTGCTATGAA[C/G]ATTAGCAAACAAGCC	84132
rs780841347	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6138070	CATTGCTCTGTGTGT[A/G]TGTGTATCCACTGAT	84132
rs780868536	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6148157	ACCCTGGGTACCAGG[A/G]TGAAACCCCGTCTCC	84132
rs780874083	snp	C/G	3.12955e-05	0.0039556	missense	USP42	GRCh38.p7	7:6153919	CCCGCTACCAAAGAA[C/G]GCGCCTGGGAGGCCA	84132
rs780874201	in-del	-/TTTC			intron-variant	USP42	GRCh38.p7	7:6126285	ATGGATACGCCACAG[-/TTTC]TTTTTTTTTTTTTTG	84132
rs780916037	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6158607	ATTTGCCCATGGAGT[G/T]CTGGGGAAACAGCCG	84132
rs780931187	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6139740	CCGCCCTGTCTAGGA[C/T]TTCATTGTCCGGGTG	84132
rs780932639	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6120026	GCTGGAGTGCAGTGG[C/T]GCTGTCTCGGCTCAC	84132
rs780939725	snp	A/C	4.24583e-05	0.00460732	missense	USP42	GRCh38.p7	7:6146153	TCATTTATAGGCTAG[A/C]AATGGCCTCTGGTAT	84132
rs780979124	snp	C/T	1.78707e-05	0.00298915	missense	USP42	GRCh38.p7	7:6154106	CGGCGTTGGCGGAAG[C/T]CCCGGAAGGGTTGAG	84132
rs781032418	snp	A/G			intron-variant, downstream-variant-500B	USP42	GRCh38.p7	7:6153198	GAATCGCTTGCACCC[A/G]GGAGATGGAGGTTGC	84132
rs781039106	snp	C/T			synonymous-codon, utr-variant-5-prime	USP42	GRCh38.p7	7:6111196	TCAGAATCAGCCTGG[C/T]AGCTCCGAGGCAGTC	84132
rs781054446	snp	C/G	3.54001e-05	0.00420699	missense	USP42	GRCh38.p7	7:6154071	CGCAAAGGGGATGAT[C/G]GCGGAGGGCCCGCGG	84132
rs781069139	snp	C/T	1.68647e-05	0.0029038	intron-variant	USP42	GRCh38.p7	7:6150377	GAGGCATGGAGCTGG[C/T]GACTGAAGCTGAAAT	84132
rs781073299	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6087340	TGGCCTAAGCGCTTC[-/T]TTTTTTTTTTTTTTT	84132
rs781128400	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6098235	TTGTCAAATACCAGT[C/T]CCATGATGTATCAGA	84132
rs781132095	in-del	-/ACCCCG	0.000169909	0.00921551	cds-indel	USP42	GRCh38.p7	7:6154550	ACGCCCCGGAGCACC[-/ACCCCG]GCCACGGCGACAGGC	84132
rs781133483	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6143264	ATTCGGTGGGAGGAG[A/C]GAGGTAAAATTGTCT	84132
rs781141629	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6093700	CCTCTTTCTCTCCCC[C/T]TCCCTTCTTTACTTT	84132
rs781161414	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6113186	AGGTGTAGGCCACTG[C/T]ACCCGGACAACAGTA	84132
rs781164003	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6120613	CCTAGGCCATCTTTA[C/G]TTTCTCGTTGCCCAG	84132
rs781211722	in-del	-/TCTT			intron-variant	USP42	GRCh38.p7	7:6127854	TTGGGGGGATTAACA[-/TCTT]TCTTTACTATGTCCC	84132
rs781214320	snp	A/G	1.6612e-05	0.00288196	intron-variant	USP42	GRCh38.p7	7:6140234	TAAAATGATACACAC[A/G]TGTGGTTAAAAAATG	84132
rs781219940	snp	A/C	2.10396e-05	0.00324335	intron-variant	USP42	GRCh38.p7	7:6135991	ATATTTGTATTTATT[A/C]CCTAGTTATACTTTT	84132
rs781246103	snp	C/T	2.03872e-05	0.00319267	intron-variant	USP42	GRCh38.p7	7:6111378	AAAAGGATCAAGGTA[C/T]TGTTTTTCAAAAGAG	84132
rs781248612	snp	G/T	0.000395726	0.0140608	missense	USP42	GRCh38.p7	7:6154591	CCTGGCGAGCGCCGC[G/T]CTCTGGGCAGGTGCA	84132
rs781251225	snp	A/C/G	3.68204e-05	0.00429058	missense	USP42	GRCh38.p7	7:6154156	TCGGAGGAGCCCTGC[A/C/G]AGCAGCCACTCCTTG	84132
rs781271371	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6138686	GTGAGCATCCCCACC[C/T]GAGCTCCGCCTCCTG	84132
rs781282283	snp	C/G	0.000124977	0.00790397	missense	USP42	GRCh38.p7	7:6155192	ACCGAGACCGCGACT[C/G]CAGGTGAGCCTGGGG	84132
rs781298236	snp	A/T	1.6601e-05	0.00288101	intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6115314	ACTCTTTCTTGTTTA[A/T]TTTTCTAGCCCTAGG	84132
rs781308005	snp	C/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114932	CCTGACCTCATAATC[C/T]GCCTGCCTCAGCCTC	84132
rs781367568	snp	C/T	0.000120926	0.00777486	synonymous-codon	USP42	GRCh38.p7	7:6154773	GTACGCTGCCCGGGA[C/T]TGGAAGCCCTTCCAC	84132
rs781368643	in-del	-/CAT	1.65806e-05	0.00287924	intron-variant	USP42	GRCh38.p7	7:6159413	TGGCGATTTTGCAAC[-/CAT]CATTAAAATCTCTTT	84132
rs781411597	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6148560	GTCCATTTAGTCGTT[C/T]CAGGGGTGTGGTGTT	84132
rs781413312	snp	C/T	1.6788e-05	0.00289719	missense	USP42	GRCh38.p7	7:6147776	GGTGAACTTACTCAT[C/T]CCACCCATAGCCCCG	84132
rs781420515	snp	C/T			utr-variant-3-prime	USP42	GRCh38.p7	7:6160861	GTATTTCATGTAATG[C/T]TCCTCCAAGTTAGAC	84132
rs781429188	snp	A/C			intron-variant	USP42	GRCh38.p7	7:6108738	CCCGCCTTGGCCTCC[A/C]AAAGTGCTGGGATTA	84132
rs781453319	in-del	-/GGCA			intron-variant	USP42	GRCh38.p7	7:6108165	CATTCCAGCCTGGGT[-/GGCA]GGCAGAGCTAGACTT	84132
rs781454564	snp	A/C	1.6563e-05	0.00287771	missense	USP42	GRCh38.p7	7:6149830	ACCTTCATAGTAATT[A/C]TTTGGAGAACCCTAC	84132
rs781458394	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6147981	GTAGTGGTTGCTGTG[A/T]CCTCAAATACATCTG	84132
rs781492623	snp	G/T			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114115	TAGTCTCCTCACAAG[G/T]GTGTACAGTGGTACC	84132
rs781494163	snp	A/C/T	3.89886e-05	0.00441506	missense	USP42	GRCh38.p7	7:6154715	TCTACCCCGACAGGC[A/C/T]GCGCTGGGACAGGTG	84132
rs781546970	snp	C/G	1.87633e-05	0.00306289	missense	USP42	GRCh38.p7	7:6154196	GCGGGGACCACGCCC[C/G]GGACGCTCAGGACCC	84132
rs781567916	snp	A/T	1.65938e-05	0.00288039	intron-variant	USP42	GRCh38.p7	7:6140084	CACAGCATCTGGAGT[A/T]TTTGCAAAGCTCTTC	84132
rs781588395	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6152405	TGCCAGTGACACACC[C/T]GTAGTTTTTACCCGC	84132
rs781602134	snp	A/G			upstream-variant-2KB	USP42	GRCh38.p7	7:6077690	ATAGGGTGAAACTCC[A/G]TCTGTACTAAAAATG	84132
rs781602981	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6096567	GGTCTGTCAGGAGCT[A/G]GTTTAAACTAACAAG	84132
rs781607761	snp	A/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103564	GTAACTCAGTGTGTG[A/C]GTCTGATGGACAGTG	84132
rs781608181	snp	A/T	1.77985e-05	0.00298311	intron-variant	USP42	GRCh38.p7	7:6147720	GTGTCACCCTAAGTA[A/T]CGCTCTCCTTGTTTC	84132
rs781615365	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6122497	TTGTTTTGAGACAGA[A/G]TCTTGCTCTGTTGCC	84132
rs781645883	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6096143	CACTGAGACAGCTAA[C/T]CTCAGTCTTCTACAC	84132
rs781663588	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6084050	GTTTTGTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	84132
rs781670994	snp	A/G	4.24845e-05	0.00460874	splice-donor-variant	USP42	GRCh38.p7	7:6157056	TTGAGTATGGCCAGG[A/G]TAAGAGGAGATACTT	84132
rs781676693	snp	A/G	1.73788e-05	0.00294772	intron-variant, utr-variant-5-prime	USP42	GRCh38.p7	7:6116847	TTTTGCGCTTAATGA[A/G]AGTAGGGTGTGGATG	84132
rs781679130	snp	A/G	1.83984e-05	0.00303296	missense	USP42	GRCh38.p7	7:6150124	GCCAAGATGCCGAAG[A/G]TGAGGAGGCCACTCC	84132
rs781691595	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6099795	TGGTGAAACCCCATC[G/T]CTACTAAAAATACAA	84132
rs781703241	snp	A/C			utr-variant-5-prime, intron-variant	USP42	GRCh38.p7	7:6081740	AAGCCGACTGCGCCT[A/C]CGTGGACTGCGGGTT	84132
rs796070817	snp	G/T			intron-variant	USP42	GRCh38.p7	7:6112718	ACTTTCTTAAAACAT[G/T]GAGTTTTTTTGAGAT	84132
rs796077360	snp	C/G			intron-variant	USP42	GRCh38.p7	7:6158677	TTGCCTGCGGGCCTT[C/G]TAGACGTTCTGGACA	84132
rs796082163	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6095068	GCTGGCATTATAGGT[A/G]TGAGCCACCGTGCCC	84132
rs796212768	in-del	-/AC			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6103755	AAAAAAAAAAAAAAA[-/AC]AAAACTTAAAAAATT	84132
rs796239771	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6155296	GTGACCAGCCAGGCC[A/G]CAGTTGTATCCGTCT	84132
rs796273990	in-del	-/C			upstream-variant-2KB, intron-variant	USP42	GRCh38.p7	7:6079921	TTTCACCCCCCTACG[-/C]CCCCCAAAAAAAACT	84132
rs796294675	snp	A/T			intron-variant	USP42	GRCh38.p7	7:6134889	CTCCCTGGGATCAGG[A/T]GATCCTCCTGCCTCG	84132
rs796342852	in-del	-/T			utr-variant-3-prime	USP42	GRCh38.p7	7:6160807	CTGGAATAGAACATC[-/T]TCAAATGCTGCTTAA	84132
rs796386554	in-del	-/T			intron-variant	USP42	GRCh38.p7	7:6123884	TTCGTATCGTTTCTC[-/T]TTTTTTTTTGAGGTG	84132
rs796405541	in-del	-/CCAT			intron-variant	USP42	GRCh38.p7	7:6130449	CGGGGGCTGGGGAGG[-/CCAT]AGTGGTGGCAGAGTT	84132
rs796467919	snp	C/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6114488	AATCCAATACTTCAT[C/G]TTTCACTTGTATTTT	84132
rs796517486	in-del	-/CGCCAGCCATGTCTT			intron-variant	USP42	GRCh38.p7	7:6139210	GTAAGTACAACAGAG[-/CGCCAGCCATGTCTT]CATTGGGGATCTCTG	84132
rs796544660	multinucleotide-polymorphism	AT/GC			intron-variant	USP42	GRCh38.p7	7:6123378	TAAAATATTAAAAAA[AT/GC]GGGCTGGGTGCGGTG	84132
rs796549387	snp	C/T			intron-variant	USP42	GRCh38.p7	7:6112341	ATAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	84132
rs796562622	in-del	-/A			intron-variant	USP42	GRCh38.p7	7:6145344	TCAAAAAAAAAAAAA[-/A]GATGGCTAAATGCAC	84132
rs796588992	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6152569	AAACCGGAATGGGGC[A/G]AACCCTGTGGGCAGG	84132
rs796613341	snp	C/G			intron-variant, utr-variant-3-prime	USP42	GRCh38.p7	7:6152989	AACTAGAGGAATTGC[C/G]GCCAGGCGCGGTGGC	84132
rs796654189	in-del	-/TAGT			downstream-variant-500B, utr-variant-3-prime	CYTH3, USP42	GRCh38.p7	7:6161282	GTCCCTTCGAGTTTC[-/TAGT]TAGTTACAGACACAA	84132
rs796759092	in-del	-/AG			intron-variant	USP42	GRCh38.p7	7:6122494	TGTTTGTTTTGAGAC[-/AG]AGTCTTGCTCTGTTG	84132
rs796797126	snp	C/T			missense	USP42	GRCh38.p7	7:6154964	TCTCCCACGACAGAA[C/T]TGCACTTGTAGCCGG	84132
rs796865853	in-del	-/G			intron-variant, upstream-variant-2KB	USP42	GRCh38.p7	7:6113899	GTGCTGGGATTACAG[-/G]CATGAGCCACTGTGC	84132
rs796927927	in-del	-/TTTTTTTTTTT			intron-variant	USP42	GRCh38.p7	7:6087341	TGGCCTAAGCGCTTC[-/TTTTTTTTTTT]TTTTTTTTTTTGAGA	84132
rs796945706	in-del	-/AC			intron-variant	USP42	GRCh38.p7	7:6116121	AAAAAAAAAAAAAAA[-/AC]GTCTGATGCCAGCAA	84132
rs796948230	snp	A/G			intron-variant	USP42	GRCh38.p7	7:6100006	AAATTTCACAAGTCT[A/G]TTATTATTATTATTA	84132
rs796990848	multinucleotide-polymorphism	CG/TC			missense	USP42	GRCh38.p7	7:6153889	AGGCTCCGCCGCCCC[CG/TC]GATCCCGGCACCCCC	84132
rs797002915	in-del	-/GGCCA			intron-variant	USP42	GRCh38.p7	7:6113110	GGGTTTCACCATGCT[-/GGCCA]GGCTGGTTTCAAACT	84132

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