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

CHD4

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs527780701	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6594085	GGTGATCCACCAACC[C/T]CGGGCTTCCAAAGTG	1108
rs527813886	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6579828	TTGGGAGGCCAAAGC[A/G]GGCGGATCACGAGGT	1108
rs527814383	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6586711	TTTTTTGTTGTTTTT[C/T]TTTTTCAAACACAGT	1108
rs527854546	snp	A/G	0.0023933	0.0345097	intron-variant	CHD4	GRCh38.p7	12:6590707	AAGCCTACAGCCCCA[A/G]CTAGTTGGGAGGCTG	1108
rs527975622	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6605185	GCTAAGAAGAGAGAA[A/G]GCAGAAGTGAATGAT	1108
rs527995413	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595090	TGGCCCCTCCCCCCA[A/G]ACAACACTTCTTCAA	1108
rs528120328	snp	C/G/T	1.70058e-05	0.00291592	synonymous-codon	CHD4	GRCh38.p7	12:6606308	GCTGTTGTTCAAAAG[C/G/T]GCATCCATATCCTCC	1108
rs528161710	snp	C/T	1.64749e-05	0.00287005	missense	CHD4	GRCh38.p7	12:6600336	CGCCTTGCTGGCACA[C/T]CTCGCAATAGTCCTG	1108
rs528179365	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6596732	TTGAACCCGGGCGGC[A/G]GAGGTTGCAGCAAGC	1108
rs528289858	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580267	ACAACAAATAAAGTC[A/G]TAAGAGATACCTTAA	1108
rs528324590	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6573462	TCCCTTTTTCAATGT[C/T]CTCATTTTTAAAACT	1108
rs528407420	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6578992	CACTATTATCCAATT[A/G]GATAGACCCACATCT	1108
rs528549617	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575748	TAAAGTCCAAACTCT[C/G]TTATCTGGTGCCAAG	1108
rs528603941	in-del	-/C	0.211819	0.247067	intron-variant	CHD4	GRCh38.p7	12:6580241	CGAAAACAACAACAA[-/C]AACAACAACAACAAC	1108
rs528668895	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6595243	ACAAAGTTACTATCT[A/G]CATTTCATTACTTAA	1108
rs528681840	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6598676	TAGCTGGGCGTGGTG[A/G]CATGCGCCTGTAGTC	1108
rs528695304	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6587639	TCCCACAAGACCCTT[A/G]GTATCAAAGATTCTC	1108
rs528869914	snp	A/G	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6596693	TAATCCCAGCTACTC[A/G]GGAAGCTGAAGCAGG	1108
rs528890764	snp	G/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6590170	GCCACTGCACTCCAA[G/T]CTGGGCAACAGAGTG	1108
rs528982024	snp	A/C	0.00398564	0.0444627	intron-variant	CHD4	GRCh38.p7	12:6576502	GTATTTTTTGTAGAC[A/C]TGGGGTTTTGCCATG	1108
rs528997777	snp	C/T	0.00199481	0.0315187	intron-variant	CHD4	GRCh38.p7	12:6588795	AAAAAAAAAAAAAAA[C/T]TTAGCTGGGAATGGT	1108
rs529037725	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608052	GAAACTCACCCCCCC[A/C]CATACTACAACAACG	1108
rs529065724	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6575363	TGAGGCAGGAGAATC[A/G]GTTGAAGCCAGGAGG	1108
rs529117126	snp	C/T			splice-donor-variant	CHD4	GRCh38.p7	12:6577784	CTCCCCAACCGCTCA[C/T]CTTAAACCTTCGAGC	1108
rs529130912	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6604301	GAAAATAATATCCCT[C/T]CTTCAATCCCTGACA	1108
rs529131354	snp	A/C	0.00517822	0.0506191	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608534	ATTCTTCCCACCCCC[A/C]TCTCCAGGCGCTGTC	1108
rs529188545	snp	A/T	1.64738e-05	0.00286995	intron-variant	CHD4	GRCh38.p7	12:6602354	TCCTCTGATTCCCCG[A/T]AACATTCAGTCACCC	1108
rs529225007	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6603381	CTCTCTCCCTCTTCC[C/T]AAGCCACCCCCGCCC	1108
rs529333440	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597602	AAACCCTGTCTCTAC[C/T]AAAAATACAAAAAAT	1108
rs529461648	snp	A/C	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6577274	AAAATCCAAAAAAAA[A/C]AGCTGGGTGTGGTGG	1108
rs529497052	snp	A/G	1.6477e-05	0.00287024	synonymous-codon	CHD4	GRCh38.p7	12:6570904	GTGCCCGGTTTGCCA[A/G]GCGGCTGAGAATGTT	1108
rs529575839	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6609243	AGGGAGAACTGCTGA[A/G]CACTGTTTCCCAATT	1108
rs529727882	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572435	TATCTCAGAAAAAAA[A/G]AAAAAAAAGAGGTGG	1108
rs529766587	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572781	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG	1108
rs529848783	snp	C/T	1.77099e-05	0.00297568	intron-variant	CHD4	GRCh38.p7	12:6592369	ATGTCTAAATGGAGT[C/T]TGCTTCTGTCCCTCC	1108
rs529981208	in-del	-/G			intron-variant	CHD4	GRCh38.p7	12:6589066	TAAGCTGGCCAACGT[-/G]GTGAAACCCTGCCTA	1108
rs530022122	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6585996	TCTCAGCTACTTGGG[A/G]GGCTGAGGCAGGAGA	1108
rs530135978	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6587274	GATCAATTCATCAAC[A/G]TAAGAATTTGCCTAC	1108
rs530170950	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6573555	AAAAATTTTTAACAA[A/C]AGATAATCCCACCTT	1108
rs530172681	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580859	TAAAAATACAAAAAT[C/T]AGCTGGGCATGATGG	1108
rs530232310	snp	A/C			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582387	TAACTATGGCTCCAC[A/C]TTGAGGTAAAGCCCA	1108
rs530272623	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605776	TTCACACAGTTCAGA[A/C]AGCACAGAAAACCGG	1108
rs530356314	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598854	AAAATCTAATCCCAG[A/G]ACTCCTCCAGGGAGA	1108
rs530381261	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606858	GGGCCAGTCCCCAGA[C/T]AGGGCAGCTCTCCAA	1108
rs530395831	snp	A/G	0.000148565	0.00861745	synonymous-codon	CHD4	GRCh38.p7	12:6593595	GAGGGGCGCTCACTA[A/G]GAAGGGGCCTTTGGA	1108
rs530395868	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6599451	TCTCCAAAAAAAAAA[A/T]TTTTTTTAACAAAAA	1108
rs530462690	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6601215	TTAGGGCTGACAGAC[C/T]AGCATTCCCATGCTG	1108
rs530476011	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6600450	ACTACCTCCCCCCAC[C/T]CCCCGACCCCTATCT	1108
rs530538791	in-del	-/T			intron-variant	CHD4	GRCh38.p7	12:6572685	CCTCAGCCTCCTGAG[-/T]TAGCTAGGATTATAA	1108
rs530631817	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6574411	GCAAAAACACTCATG[C/T]ACATGTCATCTGATG	1108
rs530791212	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6579401	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC	1108
rs530960213	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608135	TATACTGACATCCCA[C/T]AATAACTAACCCCCT	1108
rs530974470	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6588639	AAAAATTAGCCAGGC[A/G]TGGTGGTATACACCT	1108
rs530987460	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6570051	CACACACTCATCCAC[C/G]TGCACCTACACCCAC	1108
rs531136785	snp	C/G	1.71179e-05	0.00292552	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581717	GGTGTAGGAGTTTTT[C/G]GGGAGGGTGACCCTG	1108
rs531145246	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575922	CCCAACCTAATCCCT[C/T]TGTTCAGATACCCTT	1108
rs531305357	snp	A/C	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6577433	AAAAAAAAAAAAAAA[A/C]AAAAAACAACCAGCA	1108
rs531323843	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6597826	TTACTGGTGACAGCC[A/G]TTTTCCCAATCTCTT	1108
rs531341655	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571040	TTTCAGAACTGCATA[A/G]GGAGAAAAAGAGGTG	1108
rs531448306	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596753	TGCAGCAAGCTGAGA[C/T]TGCGCCACTGCACTC	1108
rs531613549	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6590227	ATCTGTATCATATAA[A/G]AAAATAAAGAAATGT	1108
rs531692131	snp	A/C/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6598584	GGGAGGCCGAGGCGG[A/C/G]CAGATCACGAGGTCA	1108
rs531955924	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571758	TGAGATCAGGAGTTC[A/G]AGACCAGCCTGGCCA	1108
rs531972518	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6594947	CCAGGTAAATAATCG[C/T]TATGTCCCTCTTAGA	1108
rs532092420	snp	C/T	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6605845	ACCAGCACTCCCTCT[C/T]TCCTTTCCACAGCAG	1108
rs532142257	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6593356	ACCAGATCACAAGGA[A/G]GTAAACTAAGCCAGA	1108
rs532179081	snp	C/G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6586094	AACAGAGCAAGACTC[C/G/T]GTATCAAAAAAAAAA	1108
rs532427710	snp	C/T	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6579778	AAAAAAAATTTTGGC[C/T]AGGCGTGGTGGCTCA	1108
rs532473013	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572839	TGCTGGGATTAGAGG[C/T]GTGAGCCACCGCGCC	1108
rs532555800	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580938	CTCGAACCTGGGAGG[C/T]GGAGGTTGCAGTAAG	1108
rs532600393	in-del	-/CAT	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6589480	GAACTGAAAAGGACA[-/CAT]CATCGACTGGGCGTG	1108
rs532612008	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6586194	ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	1108
rs532637406	snp	C/T	1.66832e-05	0.00288814	intron-variant	CHD4	GRCh38.p7	12:6600202	TCCAAGGGGCCACAA[C/T]GGCCAGACACTCACG	1108
rs532673049	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6594861	AGACCTGATTTTGAT[C/T]CTACAGATCACTGAG	1108
rs532676336	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6589682	TGAGGCAGCAGAATG[C/G]CTTGAACCCGGGAGG	1108
rs532782667	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6594234	CTGCTAATCCTACCC[A/T]GGGCTCCATGCCCTC	1108
rs532801817	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6604126	CTAAAAAAACAAAAA[C/T]TAGCCAGGCATGGTG	1108
rs532830084	snp	C/G	1.6577e-05	0.00287893	intron-variant	CHD4	GRCh38.p7	12:6596167	GAGAAAACCCTCAGA[C/G]CCAGAAAAGGCAACC	1108
rs532866382	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6589495	CATCATCGACTGGGC[A/G]TGGTGGCTCACGCCT	1108
rs533030954	in-del	-/GCCCCAGCACACTGCA	0.000513031	0.0160079	intron-variant	CHD4	GRCh38.p7	12:6593649	GAGTCAGGACTGAGG[-/GCCCCAGCACACTGCA]GCCCCAGCACACTGC	1108
rs533083524	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6575211	CCAGCACTTTGGGAG[A/G]ACAAGGCGGGCAGAT	1108
rs533117710	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608607	CCCACGCTTCCTTGT[C/T]CCCGCCCCCACTTGC	1108
rs533137382	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6604171	TCCCAGCTACTCAGG[A/G]GGCTGAGGCAGGAGA	1108
rs533210327	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606909	TCAGGTTCTCCTCAA[A/G]AGCTGCGGGGACGAG	1108
rs533235157	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6603181	TCACCATCTCCCCTA[C/T]ACCCGCCCCCCAGCA	1108
rs533239676	snp	C/T	0.000231126	0.0107475	synonymous-codon	CHD4	GRCh38.p7	12:6601389	CTCCACCACAGCTAC[C/T]GCTGCTGCTGCCGCA	1108
rs533249376	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6607948	CAGCACTTATGCCTC[A/G]TATCCCATAATATTC	1108
rs533353392	snp	A/G	1.79712e-05	0.00299755	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583429	GAAGTCAGCACCACC[A/G]GCTACCCCTGGTCCT	1108
rs533440996	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6576447	AGCCTCCTAAGTAGC[C/T]GGAACTACAGGTGCA	1108
rs533477869	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6577105	CCGCACCTGGCCCAC[A/G]CAGGCACTTTTTAGC	1108
rs533487633	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570197	CATTTAGCCGCTCAG[G/T]GGCTAGAGCCGCTGG	1108
rs533802176	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571154	TGTATTGTCTTCTGT[A/C]ATCTGACCTGACCTC	1108
rs533817458	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6609370	AAGGATTTATGGGTA[C/T]AGACCATAGTCAACA	1108
rs533871420	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570574	CATGGAAGATGGGCA[C/G]AAGGAAGGTGAGGGT	1108
rs533877061	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6596526	GGCATCAGGCCGGGC[A/G]CGGTGGCTCACGCCT	1108
rs533899183	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6603614	CAAATTACCTGGCCC[C/T]AGGTCCAAATGCCAC	1108
rs533910738	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6592908	TTCACTGCCCAATAG[C/T]TAAGCATCCCACTCC	1108
rs533921472	in-del	-/A	0.00018521	0.00962137	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581182	TGTACACTTCAAAGG[-/A]AAAAAAAAACAAAAA	1108
rs533949329	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585653	AATTAGCTGGGTGTG[A/G]TGGCACGTGCCTGTA	1108
rs533986611	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6583679	CTGATGCATATACAA[C/T]TGAAAGATAGCAAAA	1108
rs534024969	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6579178	AAATTAGCTGGGTGC[A/G]GTGGCTCATGCCTGT	1108
rs534056864	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572622	TGTGCAATGGCACAA[C/T]CTTGGCTCACTGCAA	1108
rs534071730	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576899	TTATTAGTGTACCAT[C/T]TCTTCCCCGATTATA	1108
rs534112031	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6577543	CAGTGTTCCCCAAAC[A/C]AACCCCTCTGCACTA	1108
rs534280098	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598977	GAATTCCCTCTCCAT[C/T]TCTGGACATCGTCCA	1108
rs534351757	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604069	GATCATTTGAGGTCA[C/G]TTCGAAACCAGCTTG	1108
rs534406323	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6594265	AAATCTTCCGCTGTG[A/T]ACATGTGTTTATCCA	1108
rs534525791	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6572890	TAAAAAAAAAAAAAG[G/T]CAAAGAACTACTGTC	1108
rs534535145	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6575779	AACCCACCTACTGAC[A/C]TCTAGCCCGTCCACC	1108
rs534623647	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605402	GGGCATGACATCAAC[A/C]ATCATTTGAGGATAG	1108
rs534660476	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6593928	GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC	1108
rs534843523	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569657	CCGGGGGTGTGGGAT[C/T]GAGGCTGTGTTCTTC	1108
rs535141018	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607022	CCACGTGTCCCGGGG[A/G]GCAAGTGATCAAAGG	1108
rs535242623	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580424	GCTTAATATGGATAC[C/T]GGCCAGGCATGGTAG	1108
rs535331959	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580969	CCAAGATCGCGCCAC[A/G]GCACTCCAGCCTGGC	1108
rs535367868	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6574578	TTCTCCTCTCCTAGT[A/G]TCAGCCAGCAGTTCT	1108
rs535373489	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6588947	AAGACCCTAACTCTT[A/G]TAGAAAAATGTCAGA	1108
rs535404033	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6589565	CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCCA	1108
rs535410478	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596883	AGAATCACTTGAGCC[C/T]GAGAGGCGGAGGTTG	1108
rs535444489	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582533	CCCACTTCCCTGCAC[A/G]GCTAGGCCTAGAACC	1108
rs535496363	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597168	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	1108
rs535519630	snp	A/G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6590410	TTGTACTGCAGTTAC[A/G/T]TAAGTTATTATTAAG	1108
rs535533490	snp	A/T	0.00318978	0.0398085	intron-variant	CHD4	GRCh38.p7	12:6604516	ATCAGCCTGGATTTC[A/T]CCAGAAAGAATCATT	1108
rs535606408	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595091	GGCCCCTCCCCCCAG[A/G]CAACACTTCTTCAAT	1108
rs535607209	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6598982	CCCTCTCCATTTCTG[A/G]ACATCGTCCAGGATT	1108
rs535678917	snp	C/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6602252	TCAGGACAGCCCTGA[C/G]GCTCATCCCCAGAAC	1108
rs535760458	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6602615	AGATTCCTCTGAAGA[A/G]AACTGCTATACTCTG	1108
rs535868148	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6588099	CCCCTGCCTCCAGAC[A/G]CCACCCTCTATTATC	1108
rs536076612	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608724	ATTTCCAGACACTCG[A/G]GGGCTGGGAGCCCAC	1108
rs536251564	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6579864	GGTGGAGACCATCCT[A/G]GCTAACACGGTGAAA	1108
rs536380150	snp	C/G/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6584482	ACGGCTCACTGCAGC[C/G/T]TCGACTGCCAAGTTT	1108
rs536450054	snp	A/G	0.00597247	0.0543191	intron-variant	CHD4	GRCh38.p7	12:6577725	GACTCCCTCTGCTGC[A/G]GGACGTTACGCACTT	1108
rs536612344	snp	A/C	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6579277	CAACATGGTGAAACC[A/C]TGTCTCTACTAAAAG	1108
rs536646872	in-del	-/CCA			intron-variant	CHD4	GRCh38.p7	12:6605927	CCTCAACGCCCCCCT[-/CCA]CCACCACCACCACCA	1108
rs536795402	snp	C/G/T	0.000197682	0.00994023	intron-variant	CHD4	GRCh38.p7	12:6591879	CCCACATGGAGAAGA[C/G/T]CCAACCCAGGGAGGA	1108
rs536847529	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6576696	CTGCAACCTCCGCCT[C/T]CCGGGTTCAAGCGAT	1108
rs536879694	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6605937	CCCCCTCCACCACCA[C/T]CACCACAAGCCTCCA	1108
rs536888113	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6592984	AGGAAGGAAGGCAGA[A/G]ACAATTTTCCCCTCT	1108
rs536927514	snp	A/G	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6585725	ACCCGGGAGGCGGAG[A/G]TTGCAGTGAGCCGAG	1108
rs537039826	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607344	CGGCTCGGTGTCACT[C/G]CCGCTCCGGCTCCTC	1108
rs537127886	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580470	CCAGCACCTTGAGAG[A/G]CCAAGGCAGGTGGAT	1108
rs537163706	in-del	-/TTTCT			intron-variant	CHD4	GRCh38.p7	12:6576606	TGCCTCTCTGAGAAC[-/TTTCT]TTTCTTGTCTTTTTT	1108
rs537239038	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605358	AGGGGCTCTGAAAAA[A/G]GACACAGAAGAGAAA	1108
rs537258289	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6574634	ACATGTACCTTCAGC[A/G]CTGGTTCTGATCCCA	1108
rs537283080	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6599001	TCGTCCAGGATTTGC[A/G]TGCCACCATCACTCC	1108
rs537336533	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6590899	GGAGGCCGAGGTGGG[C/T]GGATCATGAGGTCAG	1108
rs537455604	in-del	-/A			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607716	CACACACACACACAC[-/A]ACACACACACACCCT	1108
rs537456489	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569886	TAAGCGGCGGTGCCC[A/G]CAGTTTTGCAGCCTC	1108
rs537546275	snp	A/C/G	0.000798403	0.0199641	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570397	CACAACAGTTTGTGT[A/C/G]TAACAGGCGTTACAG	1108
rs537560339	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595624	GAAACCCCGTCTCTA[A/C]TAAAAATACAAAAAT	1108
rs537747859	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575319	CAGGCATGGTGGTAC[A/C]TGCCTGTAATCCCAC	1108
rs537751779	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606478	AGGGGGGAGAAACAC[A/C]GAACAGTCAGTGACG	1108
rs537804383	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6590997	GCGTGGTGGCACACG[C/T]CTGTTGTCCCAGCTA	1108
rs537813258	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6583622	GAGCTATTATCACAG[G/T]TAAGGATGAAGAGAC	1108
rs537859322	snp	A/G	1.65064e-05	0.00287279	synonymous-codon	CHD4	GRCh38.p7	12:6592458	CATGTTCTTGAACAC[A/G]TCGGCTTTGAGCCGC	1108
rs537891438	snp	A/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6584410	TATAAATATATATAT[A/T]TTTTTTTGAGAGAGG	1108
rs538046757	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602723	AGACCAGGCCCACCT[C/T]GGGCAGCTGTCCAGA	1108
rs538079870	snp	C/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6589628	AAAAATTAGCCGGGC[C/G]TGGTGGCGGGTGCCT	1108
rs538189327	in-del	-/TTTTCCCCTCTCCTCTCCATCTACAAG	0.0123036	0.0774623	intron-variant	CHD4	GRCh38.p7	12:6592989	GGAAGGCAGAGACAA[-/TTTTCCCCTCTCCTCTCCATCTACAAG]TTTTCCCCTTAATGA	1108
rs538196314	snp	C/G			missense	CHD4	GRCh38.p7	12:6593225	ATTTCACAGATGCCT[C/G]TTTCTGCACATGAAG	1108
rs538212538	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6571152	GATGTATTGTCTTCT[A/G]TCATCTGACCTGACC	1108
rs538275523	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605345	AGGTGACACAGCTAG[C/G]GGCTCTGAAAAAGGA	1108
rs538371950	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598923	ACCAGAAGTATTTTG[G/T]ATTTCACATTTTTGG	1108
rs538416679	in-del	-/A	0.0126979	0.078662	intron-variant	CHD4	GRCh38.p7	12:6593977	AGTAGCTGGGATTAC[-/A]GGCGTGCACCACCAC	1108
rs538462074	snp	A/G	0.0103295	0.0711199	intron-variant	CHD4	GRCh38.p7	12:6603562	TTTGAGAGAGGTGGG[A/G]TGGCGGGGGGGGAGA	1108
rs538464562	snp	C/T	0.286825	0.247273	intron-variant	CHD4	GRCh38.p7	12:6579175	CAAAAATTAGCTGGG[C/T]GCGGTGGCTCATGCC	1108
rs538662596	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6573795	TTGGGAGGCTGAGGC[A/G]GGCAGATTACTTGAG	1108
rs538673743	snp	A/C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598489	GAAGGGACAGCCCAC[A/C/G]GTCTCAACTTCATCA	1108
rs538710424	snp	C/T	0.00222333	0.0332674	synonymous-codon	CHD4	GRCh38.p7	12:6593223	GAATTTCACAGATGC[C/T]TCTTTCTGCACATGA	1108
rs538798178	snp	C/G/T	0.000125564	0.00792269	intron-variant	CHD4	GRCh38.p7	12:6578739	ACAGTCTTTTATCTT[C/G/T]GGATAAAATGGCTAG	1108
rs538993312	snp	C/G	4.94588e-05	0.00497262	intron-variant	CHD4	GRCh38.p7	12:6573047	AGGGAGGCCGAATCG[C/G]CAGGAGGCAGGGGAG	1108
rs539054337	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6588801	AAAAAAAAATTTAGC[C/T]GGGAATGGTGGCACA	1108
rs539140334	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581875	GCTCCTTTCCTATTG[A/G]CCTTCCAGTCTCCGC	1108
rs539159943	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6606072	GAGTGCAGCAAGCTG[C/G]CATCTCCGTGCCCAG	1108
rs539189249	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575379	GTTGAAGCCAGGAGG[C/T]AGAGGGTGCAGTGAG	1108
rs539205194	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585817	CACACACACAAAGAG[G/T]CCAGGCGTAATGGCT	1108
rs539282228	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6586322	AGAAGAATGGCATGA[A/G]CCCGGGAGGCAGAGC	1108
rs539320883	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6586931	TCAAACTCCTGGCCT[C/G]AAGTGATCTGCCTGC	1108
rs539337218	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595064	TGTAAGTGCATAAAA[C/G]CTAGGCTATGTGGCC	1108
rs539377198	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6579988	GTGAACCCGGGAGGC[A/G]GAGTTTGCAGTGAGC	1108
rs539390140	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595550	GCCAGCACTTTGGGA[G/T]GCTGAGACGGGCGGA	1108
rs539493692	snp	C/T	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6602590	GACTTTATTCCCCAC[C/T]TCTTGTCCCAGATTC	1108
rs539677132	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB	CHD4	GRCh38.p7	12:6607465	GGCCCCGCCCCCCCA[A/C]GGACAGCCCATAATA	1108
rs539697240	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6598504	AGTCTCAACTTCATC[A/T]AAGGACGATTCAGAT	1108
rs539757855	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6601140	GCTTGCTTCCCCACA[C/T]TCAGATTCCCAAATT	1108
rs539769266	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608212	ACCCCCAGCCTTCCC[G/T]CTTCTAGCTCCACAG	1108
rs539832524	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6596797	AGAACGAGACTCCAT[C/T]TCAAAAAAAAAAATT	1108
rs539881781	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596671	CGGGCATGGTGGCAG[G/T]TGCCTGTAATCCCAG	1108
rs539904123	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596787	CCTGGGCGACAGAAC[A/G]AGACTCCATTTCAAA	1108
rs540120314	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569625	GTTTCAAGGTTGGAG[A/G]ACGTTAGGTCGGGCC	1108
rs540182830	in-del	-/C	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6605558	CTAAACCGCAGGCTA[-/C]CTCATAGAGACAGAA	1108
rs540229543	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608887	ACCCTACAGCATCCC[A/G]TAATAATTACCAACT	1108
rs540279889	snp	C/T	0.0023933	0.0345097	intron-variant	CHD4	GRCh38.p7	12:6589351	ATTTATCAATCACAA[C/T]GGGAACAATAGAAAC	1108
rs540332707	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6603925	TCCCACCCAGATTCC[C/T]ATCCAACATATGGGA	1108
rs540472922	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6584095	ACCATAGATGGAAAA[C/T]ATTCAGAGAAAAAAC	1108
rs540493602	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6593950	AAGCGATTCTCCTGC[C/T]TCAGCCTCCCAAGTA	1108
rs540512188	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569956	TACTGCACCCACACA[C/G]AGAACCCAGTTACTC	1108
rs540518733	snp	A/C	0.0023933	0.0345097	intron-variant	CHD4	GRCh38.p7	12:6591134	TCTCAAAAAAAAAAA[A/C]AAAAAAAAAAAAAAA	1108
rs540852336	in-del	-/A	0.00199481	0.0315187	intron-variant	CHD4	GRCh38.p7	12:6597781	AAACAAAAAACAAAC[-/A]AAAAAAAACCAGTGT	1108
rs540950694	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598547	CTGGAGCAGTGGCTC[A/G]TGCCTGAAATCCCAG	1108
rs540984293	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6585408	TCTGCCTCAGCCTCC[C/T]GAATAGCTGGGACTA	1108
rs541008985	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6574334	TACATGTTTCACCTA[G/T]GCATTCTCCTAATGC	1108
rs541237797	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6599384	GTTGGAGGCTGCAAT[A/G]AGCTATGACTGCACC	1108
rs541341290	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6592223	AATAAGGAAAGGTAT[A/C]ACCTAAAATAAGTAA	1108
rs541364799	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605740	AGCACTCCAGATCCT[A/G]CTGAGGAGCGCGATT	1108
rs541373848	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6597422	TATGAGCAGTGATCA[C/T]GACACTGCACTCAAG	1108
rs541388103	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6574963	GGCAAAAAGTCAAAA[C/T]AAGACTATTTCATGC	1108
rs541407059	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6606158	CCTTCGGATACCCTC[C/T]ACCTCCGGCTCTGCA	1108
rs541443614	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6594111	AAGTGCTGGGATTAC[A/C]GGTATGAGCCACTGC	1108
rs541528239	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606600	AGTTCCACACTCCTC[A/G]GGGGCAGCCCGGAAG	1108
rs541602188	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572731	CATGCCCAGCTAATT[C/T]TTCTATTTTTAGTAG	1108
rs541611849	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6587268	GAAGAGGATCAATTC[A/T]TCAACATAAGAATTT	1108
rs541612323	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6580082	AAAAAAAAAAATTAC[A/G]TGGGCATGGTTGTGG	1108
rs541662135	snp	C/T	0.00874735	0.0655527	intron-variant	CHD4	GRCh38.p7	12:6576938	ACGAGACAACAGACA[C/T]GTCTTTTTTTTTTTT	1108
rs541708041	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6574271	TACTCTTATGTTGTA[C/T]GCACATGAATTTTGT	1108
rs541817083	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6603322	CCAGGAGGCAGCTTC[C/T]TTTGTAACAGACATT	1108
rs541913122	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	CHD4	GRCh38.p7	12:6607654	ATCCCATAATACACA[C/T]GGACACCCCCCCCCC	1108
rs542006656	snp	C/T	1.6498e-05	0.00287206	intron-variant	CHD4	GRCh38.p7	12:6601795	AAAGTCAAGTAAGTA[C/T]CTGCCACCTAGTGCC	1108
rs542043450	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595877	GCAGGAGAATCGTTT[C/G]AACCAGGAAGTCGGA	1108
rs542056149	snp	C/G	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6588114	ACCACCCTCTATTAT[C/G]ATGTTACCCAAAATA	1108
rs542132993	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6596519	TTAGCCAGGCATCAG[A/G]CCGGGCGCGGTGGCT	1108
rs542156374	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6589974	GAGGCCAAGGCGGGC[A/G]GATCACCTGAGGTCA	1108
rs542329893	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6576328	TGCCACTGCACTCCA[A/G]CCTGGCAACACATCA	1108
rs542584311	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572183	CCTATAATCCCAGCA[C/G]TTTGGGAGGCGGAGG	1108
rs542637169	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597037	CACTTTGGAAGGAGG[A/T]GGTGAGCGGATCACA	1108
rs542671489	snp	A/C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597364	CTAACACTTTGGGAA[A/C/G]CTGAAGCAGACAGAT	1108
rs542870901	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608961	TCACCACATCCCCAG[A/G]TCAGGGATCTTTCAC	1108
rs542891910	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585183	CTCTATATCATTTAG[A/G]AGAGAAAAACATTAA	1108
rs542913961	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602994	AACCACTTTGAAGTC[A/G]TCACTGCTCAAATTA	1108
rs542937034	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6579020	TCTAAATGTCTGCAA[C/T]TACAGTAATGTCAGC	1108
rs542968553	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6586542	CCATCCTGGGCAACA[C/T]AGCAAGACATCTCTA	1108
rs542984134	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6573980	GTGAGCCAGGATCGC[A/G]CCACTACACTCCAGC	1108
rs543244465	snp	A/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6593328	CCAGGGTTACCCTTT[A/T]GCCTCACCAGGGACC	1108
rs543252472	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6578238	CATCCCCTACCCCTG[A/G]ATCCATTTCATATAA	1108
rs543359652	snp	A/C	0.00438332	0.0466095	intron-variant	CHD4	GRCh38.p7	12:6579754	AGACTCCGTCTCAAA[A/C]AAAAAAAAAAAAAAA	1108
rs543367499	snp	A/G	0.00478085	0.0486577	intron-variant	CHD4	GRCh38.p7	12:6585957	ATAAAAAAATTAGCC[A/G]GGCATGGTGGTGCAT	1108
rs543601543	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570411	TGTAACAGGCGTTAC[A/G]GTGGGGAGAAGCCAG	1108
rs543608432	snp	C/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607822	CTCTTAGACATCCCA[C/T]AATAGACATCCTTTG	1108
rs543735218	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6602884	TATAAACCAGGGAAT[A/G]AGAATGAAAGATCCT	1108
rs543830973	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6594813	TGCAATTTCATGTTC[A/G]GTTTAGGGTCCTCCA	1108
rs543865611	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6595162	AGAAGAAAGTAATCC[C/T]AGTGCTTTCTGATAT	1108
rs543952627	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6588160	AAACTCTGGCTTACA[A/G]TAAGGTAAACAACAC	1108
rs543967794	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6574009	GCCTGAGTGACAGAG[A/G]GAAACTGTCTCAAAA	1108
rs543992350	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605779	ACACAGTTCAGACAG[C/T]ACAGAAAACCGGTAA	1108
rs544032396	snp	C/G	1.64893e-05	0.0028713	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581462	ATTTCTTCCCAGTTT[C/G]TCTCATCTTAAATTG	1108
rs544123766	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575107	ATGGAGTTGAGTATA[C/T]GCAACAGAGACTACA	1108
rs544156183	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6583964	TATATTGGAATTAAA[C/T]AGCTGCTAATAGCAT	1108
rs544224759	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	CHD4	GRCh38.p7	12:6607766	ACATATGCCAGAGAC[C/T]GCTGACATCTCAAAA	1108
rs544259979	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608398	TAATAATTGCAAGGA[A/G]CCCGTGGTCAACCAA	1108
rs544311397	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6609051	TGCTCTATACACACC[A/G]AGAGTGAAGGCCTGC	1108
rs544435936	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581999	GTAGAGATGGGGTTT[C/T]GCCATGTTGACCAGG	1108
rs544676650	snp	C/T	3.30557e-05	0.00406531	intron-variant	CHD4	GRCh38.p7	12:6570818	AGCAAAGTTACAAGC[C/T]CCAGAATGGTTCTGC	1108
rs544750371	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596537	GGGCGCGGTGGCTCA[C/T]GCCTATAATCCCAGC	1108
rs544871405	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6603146	CCTCTTCTCCCTAGG[C/G]GCCCGAATCAGCCCA	1108
rs544898120	in-del	-/AAAAGAC	0.000569501	0.0168649	intron-variant	CHD4	GRCh38.p7	12:6601911	GGTGTCTAGGAAACA[-/AAAAGAC]AAAAGTTTAACAGTA	1108
rs544978160	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6591317	ATAGTCCAATACATT[C/T]GTCCAATTGAGACAT	1108
rs545190442	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6599304	TAGCTGGATGTGGTG[A/G]CATGCACCAGTACTC	1108
rs545221548	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6603830	CATACAACCTTCTCC[A/C]CAAATTTCTGATACC	1108
rs545278408	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6579441	ATACAAAAATTAGCC[A/G]GGCGTGGTGGCGCAT	1108
rs545327993	in-del	-/A	0.253544	0.249975	intron-variant	CHD4	GRCh38.p7	12:6577265	CTCTACTAAAAATCC[-/A]AAAAAAAACAGCTGG	1108
rs545370702	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572707	GGATTATAAGCGTGC[A/G]TTGCGCCACATGCCC	1108
rs545417336	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6598595	GCGGGCAGATCACGA[A/G]GTCAAGAGATCGAGA	1108
rs545420719	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605172	AACTTCCACTGAAGC[A/T]AAGAAGAGAGAAGGC	1108
rs545470241	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6588576	TGACATCAGGAGTTC[A/G]AGACCAGCCTGGCCA	1108
rs545502424	snp	C/T	5.211e-05	0.00510415	intron-variant	CHD4	GRCh38.p7	12:6606241	AGCCCCAGATGTCTC[C/T]TTCCCGCCATGGGCC	1108
rs545550918	snp	C/T	0.327445	0.237702	intron-variant	CHD4	GRCh38.p7	12:6579070	CTGTAATCCCAGCAT[C/T]TTGGGAGACAGCAGC	1108
rs545587748	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572254	AACATGGTGAAACTC[C/G]ATCTCTACTAAAAAT	1108
rs545674372	snp	A/G			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582840	CCTTAGAATCGTATG[A/G]CACTTACTTCAATAT	1108
rs545676387	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580235	CCATCTCGAAAACAA[A/C]AACAACAACAACAAC	1108
rs545676486	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6587212	CAACCAAGGCAAAGA[A/T]GAAAATCTGATTAGT	1108
rs545875774	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6574669	TGTATGGTGATGGGG[C/G]TCGGTAGTGGGAGGG	1108
rs546024885	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6600819	TTGTTCTGTGGGAAA[C/T]GCCCCACATTCTTAC	1108
rs546140789	snp	C/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6595852	AATCCCAGCTACTCA[C/G]GAGGCTAAGGCAGGA	1108
rs546314503	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582515	CTTCAACAGAGAAAA[C/T]AGCCCACTTCCCTGC	1108
rs546346048	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6594343	ATCTATTATCCACAG[C/T]GTTCTTGAAGGTCAG	1108
rs546471983	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6589766	CAAGACTTTGTCTCA[-/A]AAAAAAAAAAAAAGA	1108
rs546566047	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6602596	ATTCCCCACCTCTTG[C/T]CCCAGATTCCTCTGA	1108
rs546573776	snp	C/G	0.000631943	0.0177644	intron-variant	CHD4	GRCh38.p7	12:6596181	AGCCAGAAAAGGCAA[C/G]CCTCCTCACTTCCTC	1108
rs546610756	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6589504	CTGGGCGTGGTGGCT[C/G]ACGCCTGTAATCCCA	1108
rs546622443	in-del	-/TAT	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6571140	CAAGTAACTGTGATG[-/TAT]TATTGTCTTCTGTCA	1108
rs546642856	snp	A/C/G	3.29686e-05	0.00405998	missense	CHD4	GRCh38.p7	12:6570882	ACCTGCTGTGGGGTA[A/C/G]GTTCGGGTGCCCGGT	1108
rs546653902	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6603186	ATCTCCCCTACACCC[A/G]CCCCCCAGCAAGCCT	1108
rs546692669	snp	A/C	0.00318978	0.0398085	intron-variant	CHD4	GRCh38.p7	12:6597146	CCAGGCATGGTGGCG[A/C]TGGCCTGTAGTCCCA	1108
rs546740265	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575961	ACCAAAAAAATCTCC[A/G]TCGCATTCTTCAAAA	1108
rs546743348	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596811	TTTCAAAAAAAAAAA[A/T]TAGGCAGGCGTGGTG	1108
rs546795231	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606958	CGCTGCGGGGGGCCG[C/G]AGGCAGGGACGCGGG	1108
rs546882640	snp	C/T	0.000462351	0.0151974	synonymous-codon	CHD4	GRCh38.p7	12:6601401	TACCGCTGCTGCTGC[C/T]GCAGCTGCCACTGAT	1108
rs546887197	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6607999	TCCCATAATAACCAT[C/T]CTTCATCCACCCCCA	1108
rs547201424	in-del	-/G	0.447032	0.153878	intron-variant	CHD4	GRCh38.p7	12:6571731	TTGGGAGGCAGAGGC[-/G]GGTGGATCACCTGAG	1108
rs547247769	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570208	TCAGTGGCTAGAGCC[A/G]CTGGGTTCCTGGTAT	1108
rs547314159	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608678	CAAAAAGCCTCCTGA[G/T]GTCTGGGACCCCAGC	1108
rs547388705	snp	A/G	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6584756	TTTTAAAAGAAGTCA[A/G]CAGCAGCTATAGTCA	1108
rs547453796	snp	C/T	0.110872	0.20771	intron-variant	CHD4	GRCh38.p7	12:6579089	GGAGACAGCAGCAGG[C/T]AGATCACTTGAGGTC	1108
rs547465289	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571918	GTGAACTGAGATCGC[A/G]CCATTGCTCTCCAGC	1108
rs547499258	snp	C/T	0.00279162	0.0372561	intron-variant	CHD4	GRCh38.p7	12:6579838	AAAGCGGGCGGATCA[C/T]GAGGTCAGGAGGTGG	1108
rs547885695	snp	A/G	0.0023933	0.0345097	intron-variant	CHD4	GRCh38.p7	12:6594991	CTTTAATCACCCTCA[A/G]ATTACACTGTACAAA	1108
rs547942898	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572938	TACTAACCTCCCAAG[G/T]ATGGCAAAGATCCCT	1108
rs548030036	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6573483	TTTTAAAACTCTTTA[A/C]CCTTTAGGTTCTCTT	1108
rs548042509	in-del	-/A	0.0023933	0.0345097	intron-variant	CHD4	GRCh38.p7	12:6604896	AGACGTGGAACCCAG[-/A]ATGTTTAGGCAGCAC	1108
rs548076806	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605192	AGAGAGAAGGCAGAA[A/G]TGAATGATGCTGGAT	1108
rs548105495	snp	A/G			synonymous-codon, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581129	CTCAGGGGGTTCAAC[A/G]ACGACCTTTTCATCC	1108
rs548110779	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598794	AGCCTGGGGGACAGA[C/G]CAAGACTCCATCTCA	1108
rs548226143	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605909	CTGGTCTTTCAAACA[A/G]AATCCTCAACGCCCC	1108
rs548226921	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6598968	CCTGTAATAGAATTC[C/T]CTCTCCATTTCTGGA	1108
rs548484576	snp	C/G	0.000956519	0.0218482	intron-variant	CHD4	GRCh38.p7	12:6587666	TCTCCCTAACCTTTA[C/G]AGAGGCCAAGCCCCA	1108
rs548583636	in-del	-/TTG			intron-variant	CHD4	GRCh38.p7	12:6586700	ACCCTGTCTCTTTTT[-/TTG]TTGTTTTTTTTTTTC	1108
rs548650485	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575847	CAAATGTTTCCCTAC[A/G]GCTCAACTGGGCTAT	1108
rs548702628	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608075	CAACAACGGACACTC[A/G]GCCTCCTCCCACACA	1108
rs548831684	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6590425	GTAAGTTATTATTAA[A/G]AGAAGCTAGCTAGTT	1108
rs548879139	snp	C/T	1.65236e-05	0.00287429	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581631	AGGGACAGAAAATGA[C/T]AGGACAGGCAGACTT	1108
rs548944515	snp	A/G	0.00438332	0.0466095	intron-variant	CHD4	GRCh38.p7	12:6597209	TGAACCCAGGAGGCA[A/G]AGCTTGCAGTGAGCC	1108
rs549010597	snp	A/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6589584	CCATCCTGGCCAACA[A/T]GGTGAAACCCTGTCT	1108
rs549032074	snp	A/G	0.00279162	0.0372561	intron-variant	CHD4	GRCh38.p7	12:6597664	CCAGCTTCTCAGGAG[A/G]CTGAGGCAGGATAAT	1108
rs549087691	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604003	AATATCCCAATCGGG[G/T]GCAATGGCTCATGCC	1108
rs549124129	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570304	AAAAAGGAGAAAAGA[A/C]AACACAAAATAAACC	1108
rs549141497	snp	A/G	1.72907e-05	0.00294025	missense	CHD4	GRCh38.p7	12:6602033	TTCTTCTCTTTCTTA[A/G]GTCCAAGCTTCTTCT	1108
rs549738091	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585506	CCAGGATGGGCTCGA[G/T]CTCTTGACCTCGTGA	1108
rs549820322	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604832	GCTCCTGCGCAGCTC[C/G]CGGTCAACATGAAAG	1108
rs549827770	snp	C/G	0.110167	0.207236	intron-variant	CHD4	GRCh38.p7	12:6579104	CAGATCACTTGAGGT[C/G]AGGAGTTCAAGACCA	1108
rs549938193	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580356	CCTCCTGATATCTCT[A/G]CAGCCCCAGCAAAAA	1108
rs549979787	snp	A/G	0.000457701	0.0151209	intron-variant	CHD4	GRCh38.p7	12:6578592	TCCAGCCAAAGCCCA[A/G]CACCATCGCCCTTAC	1108
rs550026026	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6573616	AGGTTTTTTTGTGCA[C/T]AGTTTTTTACATAAC	1108
rs550138109	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6594771	GAGCTCCGGAAAATT[C/T]GGAGGGAAGAGATCC	1108
rs550263535	in-del	-/T			intron-variant	CHD4	GRCh38.p7	12:6574514	TAATTACTTAAAAAA[-/T]ATATTCATAAAACAT	1108
rs550415155	snp	A/T	0.0111196	0.0737302	intron-variant	CHD4	GRCh38.p7	12:6599452	CTCCAAAAAAAAAAA[A/T]TTTTTTAACAAAAAA	1108
rs550430240	snp	A/G	1.66219e-05	0.00288283	synonymous-codon	CHD4	GRCh38.p7	12:6593614	GGGGCCTTTGGAATG[A/G]CCCTTTGAGAAAAAA	1108
rs550580615	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6599591	AACATCAACTCCTCA[A/G]TTTGAAGTTAGTCCT	1108
rs550706286	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6579413	AACATGGTGAAACCC[C/G]ATCTCTACTAAAATA	1108
rs550708661	snp	A/T	0.00438332	0.0466095	intron-variant	CHD4	GRCh38.p7	12:6574422	CATGCACATGTCATC[A/T]GATGGAGCTGTATTA	1108
rs550772886	snp	C/T	0.000250119	0.0111802	synonymous-codon	CHD4	GRCh38.p7	12:6602128	CTCCTCCACAAACTC[C/T]GGCCCCTCCCCAGAG	1108
rs550806314	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582347	GATTCTTTTCCATCC[C/G]TTCGTGAGGCATTAT	1108
rs550852941	snp	A/G	1.72196e-05	0.00293419	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581727	TTTTTGGGGAGGGTG[A/G]CCCTGGCTGGGACAT	1108
rs550904832	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606878	CAGCTCTCCAAAGGC[A/T]GTCCTCTGGGACAAC	1108
rs550934835	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575348	ACCTACTTAGGAGGC[C/T]GAGGCAGGAGAATCG	1108
rs551060658	snp	A/G	3.30022e-05	0.00406202	intron-variant	CHD4	GRCh38.p7	12:6602528	AAAGAGTGGTAGGCA[A/G]GGAAAAGATCAATAG	1108
rs551169218	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6578323	AACAGAGGTAAAGAG[A/G]TAAAGTCCCTGTACC	1108
rs551175925	in-del	-/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6609249	AACTGCTGAGCACTG[-/T]TTCCCAATTTCCTGT	1108
rs551226038	in-del	-/AT			intron-variant	CHD4	GRCh38.p7	12:6579165	ATTAAAAATACAAAA[-/AT]TAGCTGGGTGCGGTG	1108
rs551235838	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575947	ACCCTTCTGTTTCTA[C/T]CAAAAAAATCTCCGT	1108
rs551318695	snp	C/T	0.00597247	0.0543191	intron-variant	CHD4	GRCh38.p7	12:6597094	CTAACACAGTGAAAT[C/T]CCGTCTCTACTAAAA	1108
rs551364970	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6576342	AGCCTGGCAACACAT[C/T]AAGACACTGTCTCAG	1108
rs551398943	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6577469	CTGACTAATAGCTCT[A/G]CATCTTCAGAGATGC	1108
rs551435783	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571109	AGTGGACCAGCCCCC[C/G]ATCACTTCTCAGTGA	1108
rs551473849	in-del	-/G			intron-variant	CHD4	GRCh38.p7	12:6603566	GAGAGGTGGGGTGGC[-/G]GGGGGGGGAGACTGC	1108
rs551482126	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585587	ACGTCTGGCCCAATT[C/G]TAATCTTTAAAAAAA	1108
rs551502242	snp	A/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608518	ATCCCATAATATTCA[A/T]ATTCTTCCCACCCCC	1108
rs551634876	snp	A/G	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6590241	AGAAAATAAAGAAAT[A/G]TCACAGATAGCAGGA	1108
rs551896183	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6595660	GGGCATGGTGGCAGA[C/T]GCCTGTAATCTCAGC	1108
rs551906452	snp	A/G	0.323908	0.238825	intron-variant	CHD4	GRCh38.p7	12:6579176	AAAAATTAGCTGGGT[A/G]CGGTGGCTCATGCCT	1108
rs552068305	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6574892	CCAGATCTGCCCCAC[C/T]ACCTGTTTTTATATG	1108
rs552109507	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604586	CCAACCCCCATCAGC[A/T]ACATCTCACCACCCC	1108
rs552166917	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572840	GCTGGGATTAGAGGC[A/G]TGAGCCACCGCGCCC	1108
rs552221409	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598928	AAGTATTTTGGATTT[C/G]ACATTTTTGGATTAG	1108
rs552565191	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580959	TTGCAGTAAGCCAAG[A/G]TCGCGCCACAGCACT	1108
rs552587123	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581885	TATTGGCCTTCCAGT[A/C]TCCGCCTCCCGGGTT	1108
rs552617005	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6590940	CCATCTTGGCCAACA[C/T]GGTGAAACCACATCT	1108
rs552773855	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6594866	TGATTTTGATCCTAC[A/G]GATCACTGAGGAAAA	1108
rs552840312	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6587023	CTCTTAAATAAAAAC[C/T]AGAAAACACAAAGAG	1108
rs552926032	snp	C/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6587619	GCTGCAGTGGAAAAA[C/G]CAAGTCCCACAAGAC	1108
rs552927942	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580396	GACCATGGTTCACAC[A/T]GGGATCTGTAGTGCT	1108
rs553071812	snp	C/G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6588181	TAAACAACACAAAAA[C/G/T]AATCTGTTGTTTCTC	1108
rs553168330	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6607504	CAACTCCAACCCCCC[C/G]CTTCCACTACCGCCA	1108
rs553200924	snp	A/G	3.29636e-05	0.00405964	intron-variant	CHD4	GRCh38.p7	12:6601769	ATGATTTAGGCTCCT[A/G]CAGAAAGAGCAAAGT	1108
rs553206784	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608222	TTCCCTCTTCTAGCT[A/C]CACAGCCTATAGTAA	1108
rs553252360	in-del	-/AAAAA	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572428	TAGACTCTATCTCAG[-/AAAAA]AAAAAAAAAAAGAGG	1108
rs553306720	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596477	CAACATGGCGAAACC[C/T]GTCTCTACTAAAAAA	1108
rs553396698	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6589871	CCCAAACTTAAGAGA[C/T]ATTCTACAAAATAAC	1108
rs553428803	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6576920	CCCGATTATACTCAG[C/T]GTACGAGACAACAGA	1108
rs553500480	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6609414	GTTCCCTACTTACTA[A/G]GGGATTTTTCTTGGA	1108
rs553505916	snp	A/G	4.97863e-05	0.00498906	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582776	GAAACCCAGGTGAGA[A/G]GCAGCAGGTCGCATT	1108
rs553533320	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6579802	TGGCTCACGCCTGTA[A/G]TCCCCGCACTTTGGG	1108
rs553548131	snp	C/T	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6580081	AAAAAAAAAAAATTA[C/T]GTGGGCATGGTTGTG	1108
rs553582950	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608865	ACATTTACATGAAGT[C/T]TAATTCACCCTACAG	1108
rs553785846	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572090	GAGATCACGCCATTG[C/T]ACCCCAGCCTGGGCA	1108
rs553858621	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6603665	TTCACAAGAGCCCAC[C/T]CTAACATCCTAAGCA	1108
rs553997705	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6583807	AGCCTTTCTATTCTT[C/T]ATAAACTTCATAAAA	1108
rs554007807	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576230	GGCGTGGTGGCACAC[A/G]CCTGTTGTCCCAGCT	1108
rs554044768	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576921	CCGATTATACTCAGC[A/G]TACGAGACAACAGAC	1108
rs554054388	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6575878	CTGCTATTTCCAGAC[A/G]TACTAAGCTTTGCTG	1108
rs554061671	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608900	CCATAATAATTACCA[A/G]CTCCCATCCAAAGAC	1108
rs554127261	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6585703	CTGAGGCAAGAGAAC[C/T]GCTTGAACCCGGGAG	1108
rs554132173	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6577696	GAAAGTGAGAACAGT[A/G]CGCTGGATGGACAGA	1108
rs554171478	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585126	GCTGAGTGGTTTACA[C/G]AGGACAAGAAAAAGG	1108
rs554212456	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6594277	GTGTACATGTGTTTA[C/T]CCACTATCACATTTA	1108
rs554323309	snp	A/C	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6591138	AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAAACC	1108
rs554371750	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580105	GGTTGTGGCACGCCT[A/G]CAATCCCAGCTACTC	1108
rs554383284	snp	A/C	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6597790	AACAAACAAAAAAAA[A/C]CAGTGTCTTCCAAGT	1108
rs554481987	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604970	CAGCACCACAACTCC[A/G]CCCTCACCTTGGGCA	1108
rs554486369	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598988	CCATTTCTGGACATC[A/G]TCCAGGATTTGCGTG	1108
rs554565935	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6589244	ACAGTAATAATCATT[G/T]TAATCAAGGTCCACT	1108
rs554711733	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6593683	CCCAGCGAACACCCA[C/T]CACCCTGCTGCCCCC	1108
rs554799878	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605404	GCATGACATCAACCA[C/T]CATTTGAGGATAGAC	1108
rs554938185	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575526	TTTGCTGACCCCTAC[A/G]GTAAGTCACTAAGTC	1108
rs554964347	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606468	TGTGCGGGGGAGGGG[A/G]GAGAAACACAGAACA	1108
rs554976329	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6576032	GTTCCGTCCCTACTC[C/T]AATTCCCTCTCGAGA	1108
rs555021107	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6600107	GAATGCTTCCCAAAG[C/T]TCACAACCCGCAGCA	1108
rs555059844	snp	A/G	1.7808e-05	0.0029839	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582574	CAGATAGATAGCAGA[A/G]GCCCTTGCTCTAGAT	1108
rs555065427	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569801	GTTTAACTTGACAAC[C/T]GTATGAGGTATACAT	1108
rs555180302	in-del	-/A	0.335559	0.234904	intron-variant	CHD4	GRCh38.p7	12:6597113	CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAATT	1108
rs555234889	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6573895	CAGGTATGGTAGTGC[A/G]CACCTGTAACTGCAG	1108
rs555337669	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6590430	TTATTATTAAGAGAA[A/G]CTAGCTAGTTGAACA	1108
rs555487080	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608299	TACTGTCGCCCCACA[A/G]ATGGACATCTAATCT	1108
rs555579558	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595616	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	1108
rs555605454	snp	G/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6588948	AGACCCTAACTCTTA[G/T]AGAAAAATGTCAGAA	1108
rs555640208	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581930	GCCTCAGCCTTCTGA[A/G]TAGCTGGGAATACAG	1108
rs555666451	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608735	CTCGGGGGCTGGGAG[A/C]CCACCTAGGGCCCCA	1108
rs555755904	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602626	AAGAGAACTGCTATA[C/T]TCTGTACAGGAGGAA	1108
rs555848012	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576948	AGACACGTCTTTTTT[C/T]TTTTTTGAGACAGAG	1108
rs555868049	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604230	CAGTGAGCCAAGATC[A/G]CACACTGCACTCCAA	1108
rs555911445	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602262	CCTGAGGCTCATCCC[A/C]AGAACATGGCCCACC	1108
rs556386962	snp	A/C	0.00478085	0.0486577	intron-variant	CHD4	GRCh38.p7	12:6572706	AGGATTATAAGCGTG[A/C]GTTGCGCCACATGCC	1108
rs556426139	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6571472	TACCTCTAAAGTATC[A/G]CAAATGACACTGTAT	1108
rs556478324	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6579915	CAAAAAATTAGCCGG[C/G]CATGGTGGCAGGCGC	1108
rs556516303	snp	A/C	0.00517822	0.0506191	intron-variant	CHD4	GRCh38.p7	12:6571948	CCTGGGCAACAAGAG[A/C]AAAACTCCATCTCAA	1108
rs556615372	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6598621	CGAGACCATCCTAGC[C/T]AACATGGTGAAACCC	1108
rs556713473	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585193	TTTAGGAGAGAAAAA[C/T]ATTAAAACAAGCCAC	1108
rs556791751	snp	A/C	0.00199481	0.0315187	intron-variant	CHD4	GRCh38.p7	12:6593011	CTCTCCTCTCCATCT[A/C]CAAGTTTTCCCCTTA	1108
rs556828225	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6585753	GAGATCATGCCACTG[C/T]ACTCCAGCCTGGGCG	1108
rs556957004	snp	A/C/G	0.000549972	0.016575	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6580999	CGGCAGCACTACACT[A/C/G]TCTCAAAACAAACAA	1108
rs557017772	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6576626	TTTCTTGTCTTTTTT[A/G]AGGTGAGTCTCGCTC	1108
rs557106737	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605942	TCCACCACCACCACC[A/C]CAAGCCTCCAGGGGT	1108
rs557154424	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6573849	GCCAACATGACAAAA[A/C]CCCGTCTCTACTAAA	1108
rs557186241	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596427	AGCTGAGGCAGGCAG[A/G]TCGCTTGAGGCCAGG	1108
rs557191097	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606493	AGAACAGTCAGTGAC[C/G]CGCACTGTCCCCCTC	1108
rs557277014	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607346	GCTCGGTGTCACTCC[C/G]GCTCCGGCTCCTCCT	1108
rs557401460	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595638	ACTAAAAATACAAAA[A/C]TTAGCTGGGCATGGT	1108
rs557417324	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6600756	ACTCTCTCACTGGGG[A/G]CACCAGAATCCCAGC	1108
rs557483303	snp	A/T	0.00199481	0.0315187	intron-variant	CHD4	GRCh38.p7	12:6574645	CAGCACTGGTTCTGA[A/T]CCCACTAGTGTATGG	1108
rs557728666	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6584452	TTGCCCAGGCTGGAG[A/T]AGAGTGGCGTCATTA	1108
rs557764207	in-del	-/GGA	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6596890	TTGAGCCTGAGAGGC[-/GGA]GGAGGTTGCAGTGAG	1108
rs557765722	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6585069	AGAATGAGAAAAGAT[A/G]ACAAAGACCACCAGA	1108
rs557846733	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608822	TTGAGGAACACCAAC[A/C]AACCAAAATACCAAG	1108
rs557882571	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6602758	TGCCTCCTCTCTCCC[A/G]TTCCTACCAGTCCTC	1108
rs557945846	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6602707	ATAGGCCTGCCAGGC[C/T]AGACCAGGCCCACCT	1108
rs558003493	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6590535	TAAACAAGGAGTAGT[A/G]ATACTGAGCACAGTG	1108
rs558047390	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576098	GCACAGTGGCTCACG[C/T]CTGTTATCTCAGCAC	1108
rs558140608	snp	A/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6597300	AATAAAATAAATAAA[A/T]AAAGATAATAACATG	1108
rs558209937	snp	A/G	1.64789e-05	0.0028704	synonymous-codon	CHD4	GRCh38.p7	12:6591503	TTGCCGCATGTTCCC[A/G]GTGATTCCACCATCG	1108
rs558210789	snp	C/T			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569742	CCTAGAAACTAACAT[C/T]AAGGTAGTGGTTAGG	1108
rs558247471	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571524	TCAAGAACCTGAATA[C/T]GTTTAAAGTTAAAAG	1108
rs558253132	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598500	CCACAGTCTCAACTT[C/T]ATCAAAGGACGATTC	1108
rs558315042	snp	A/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6596971	CTCAAAAAATATAAT[A/T]AATAAATAAATAAAT	1108
rs558343040	snp	C/T	1.66131e-05	0.00288206	missense	CHD4	GRCh38.p7	12:6593227	TTCACAGATGCCTCT[C/T]TCTGCACATGAAGGC	1108
rs558384123	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604297	AAAAGAAAATAATAT[C/G]CCTCCTTCAATCCCT	1108
rs558418440	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572058	CTGAACACAGGAGGC[A/G]GAGGTTGCAGTGAGC	1108
rs558863669	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6573844	GCCTGGCCAACATGA[C/T]AAAACCCCGTCTCTA	1108
rs558922046	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6574160	TAGGTTTTTAAAAAC[C/T]GTTTCTGTTTCCTAT	1108
rs559046786	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6606119	ACCCCCCTCACACCA[A/G]AGCTCCGCAGAAGGG	1108
rs559048033	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606558	CAGCCACCCTAGCAG[A/G]GCACCCGAACCGCTC	1108
rs559099048	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6586641	TTAAGGTTGCACTCA[A/G]CTATGATTGTGCCAC	1108
rs559187081	snp	A/C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580259	CAACAACAACAACAA[A/C/G]TAAAGTCATAAGAGA	1108
rs559194549	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6579449	ATTAGCCGGGCGTGG[C/T]GGCGCATGCCTGTAA	1108
rs559194594	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6586368	ATCGCACCACTGCAC[C/T]CCAGCCTGGGGGAGA	1108
rs559224350	snp	C/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6580532	ACCAATATGGAGAAA[C/G]CCCCTCTCTACTAAA	1108
rs559398619	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6573437	AACTTTGCCTTGTAA[C/G]TTTTTTCTTTCCCTT	1108
rs559514209	snp	C/T			synonymous-codon, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581345	TTCTCCTTCTATGCT[C/T]TCTTCTTCTTTGAGG	1108
rs559539368	snp	A/G	5.34516e-05	0.00516943	intron-variant	CHD4	GRCh38.p7	12:6600908	CACCCTCCCTAAAGC[A/G]ATGGGCTGGGCTCTC	1108
rs559858124	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575285	AAACCCCATCTCTAC[C/T]AAAAATACAAAAATT	1108
rs559951232	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6595240	GCTACAAAGTTACTA[C/T]CTGCATTTCATTACT	1108
rs560111040	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571645	AGGCTAACCAACATG[A/G]AGAAACCCCATCTCT	1108
rs560124709	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569978	CAGTTACTCAGTGGG[C/G]TATCAGGACACCACG	1108
rs560149806	snp	A/C	0.00199481	0.0315187	intron-variant	CHD4	GRCh38.p7	12:6590168	GCGCCACTGCACTCC[A/C]ATCTGGGCAACAGAG	1108
rs560172607	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6603979	AGGACCTAGACAGTG[A/G]TAGAAGAGAATATCC	1108
rs560177633	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608500	ATACCCTTCGAGCCA[A/G]GCATCCCATAATATT	1108
rs560207481	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596679	GTGGCAGGTGCCTGT[A/G]ATCCCAGCTACTCGG	1108
rs560234946	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583509	TTGGTGTGCCTGTTT[A/G]GACCTAAGAACTTAG	1108
rs560241276	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604310	ATCCCTCCTTCAATC[C/T]CTGACATGTTCTTAG	1108
rs560246063	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6597000	ATAGGCCGAGTGCGG[C/T]GGCTCACGCCTGTAA	1108
rs560298116	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608050	CAGAAACTCACCCCC[C/T]CCCATACTACAACAA	1108
rs560451043	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6589636	GCCGGGCGTGGTGGC[A/G]GGTGCCTGTAATCCC	1108
rs560654196	snp	C/T	0.00398564	0.0444627	intron-variant	CHD4	GRCh38.p7	12:6590597	GCCAAGGCAGGAGGA[C/T]TGCTTGAGCCCAGAA	1108
rs560850387	snp	A/G	0.110872	0.20771	intron-variant	CHD4	GRCh38.p7	12:6579090	GAGACAGCAGCAGGC[A/G]GATCACTTGAGGTCA	1108
rs560875544	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	CHD4	GRCh38.p7	12:6609143	GCCGAGCTCCGCACC[A/G]TGGAGAATCAAGGAA	1108
rs560932436	snp	A/C	0.00279162	0.0372561	intron-variant	CHD4	GRCh38.p7	12:6579600	TCTCAAAAAAAAAAA[A/C]AACAACAACAAAAAA	1108
rs560934343	snp	A/C	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6572429	AGACTCTATCTCAGA[A/C]AAAAAAAAAAAAAAG	1108
rs560980904	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6592244	AAATAAGTAAGAACT[A/G]TGCGCTCCAGCGCCC	1108
rs561070676	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585449	CCACCACGCCCAGCT[A/G]ATTTTTGTATTTTTA	1108
rs561163120	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6589183	CCGGGAGGCAGAAGT[A/T]AAAAAGAAAGAATGT	1108
rs561172327	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6573960	CCCGGGAGGCAAAGG[C/T]TGCAGTGAGCCAGGA	1108
rs561195967	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6586783	GCTCATTGCAACCTC[C/T]GCCTCCTGGGTTCAA	1108
rs561250559	snp	A/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6594116	CTGGGATTACAGGTA[A/T]GAGCCACTGCGTCCA	1108
rs561276432	snp	A/T	0.000166309	0.00911739	intron-variant	CHD4	GRCh38.p7	12:6593258	AACTTGGTCACTACT[A/T]GTCAGTTCCTCTGTG	1108
rs561345901	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6605208	TGAATGATGCTGGAT[A/G]AGAAACAAAAACAGG	1108
rs561371103	snp	A/G	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6585562	GCTGGGATTACAGGC[A/G]TGAGCCACCACGTCT	1108
rs561440826	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6587269	AAGAGGATCAATTCA[C/T]CAACATAAGAATTTG	1108
rs561461442	snp	A/G/T	7.25668e-05	0.00602319	intron-variant	CHD4	GRCh38.p7	12:6573295	GATAAGAGGAAACGG[A/G/T]AGTTCGACTGATAAC	1108
rs561543696	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6571511	TTTGCTTTCCATCTC[A/G]AGAACCTGAATATGT	1108
rs561590427	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	CHD4	GRCh38.p7	12:6607734	ACACACACACCCTGC[A/C]CCCCCACATTTCATA	1108
rs561674454	snp	C/T	0.00676609	0.0577691	intron-variant	CHD4	GRCh38.p7	12:6587040	GAAAACACAAAGAGA[C/T]AGATTACCTAGGATC	1108
rs561676543	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6601843	TTTGTGTGGAAAAAT[C/G]AGAGTAACAGAGTTA	1108
rs561747109	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606701	GGGAGGGGAGACGCG[G/T]GGCTGGACCGAGCGG	1108
rs561779772	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6601126	TCTTCTCCACCTAAG[C/T]TTGCTTCCCCACATT	1108
rs561780659	snp	C/G/T			intron-variant	CHD4	GRCh38.p7	12:6598987	TCCATTTCTGGACAT[C/G/T]GTCCAGGATTTGCGT	1108
rs561803347	snp	A/G	3.29489e-05	0.00405874	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581295	CCATCTCTTACCTCA[A/G]TGGCAGTCTCAGGGG	1108
rs561901404	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580734	AAAAAAAAAGCCAGG[C/T]ACAGTGGCTCATGCC	1108
rs561929817	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595909	GTTGCAGTGAGTCAA[A/G]ATCACGCCACTGCAC	1108
rs561970714	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576347	GGCAACACATCAAGA[C/T]ACTGTCTCAGGAAAA	1108
rs562045274	in-del	-/C	0.00119737	0.0244387	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608042	TAATAGTCAGAAACT[-/C]CACCCCCCCCCATAC	1108
rs562240668	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608552	TCCAGGCGCTGTCAG[C/T]CTATTCTAACACCCA	1108
rs562304831	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6603542	GTGGCAGGGGAGGGG[A/G]TGGGTTTGAGAGAGG	1108
rs562451086	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6584597	CCATGTTGCCCAAGT[C/T]GGTCTCCAACTCCTG	1108
rs562451371	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6597379	GCTGAAGCAGACAGA[C/T]TGCTTGAGCCCAGGA	1108
rs562451480	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6590773	AGGCTGTAGTAAGCC[A/G]TGATTGTGCCACTGC	1108
rs562565649	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6609028	ATCACGATGTGAACT[A/C]AGGTTCCTGCTCTAT	1108
rs562574396	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6584286	TATAATTTGTATACA[C/T]ATAAAATATTTTTGG	1108
rs562597644	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6603041	CCTAGGTTCAGGTGC[C/T]AGCTCAATCTCATGC	1108
rs562761471	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604499	CCCCTTGGGAATGCA[A/T]CATCAGCCTGGATTT	1108
rs562769576	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571739	GCAGAGGCGGTGGAT[A/C]ACCTGAGATCAGGAG	1108
rs562803862	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598154	GTTCATTCCTTCTAT[C/T]CACAAGGCTCTTTTG	1108
rs562815430	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597045	AAGGAGGAGGTGAGC[A/G]GATCACAAGGTCAGG	1108
rs562860403	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572200	TTGGGAGGCGGAGGC[A/G]GGTGGATCACTTGAA	1108
rs562932001	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6578258	ATTTCATATAATTTG[C/T]TTCTGGCTTTCTCCA	1108
rs562957107	snp	A/C	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6605153	ATCTCTCCCAGACCA[A/C]CTCAACTTCCACTGA	1108
rs562965697	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6594737	CTCCTCACTAGTCTT[C/G]ACGGATCCTCTTGGG	1108
rs563126713	snp	A/C	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6579022	TAAATGTCTGCAATT[A/C]CAGTAATGTCAGCTG	1108
rs563127259	snp	C/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6572807	CCTCGTGATCCACCT[C/G]CCTTGGCCTCCCAAA	1108
rs563292127	snp	C/T	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6580226	AGTGAGACTCCATCT[C/T]GAAAACAACAACAAC	1108
rs563445783	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6579758	TCCGTCTCAAAAAAA[A/G]AAAAAAAAAAAATTT	1108
rs563511664	in-del	-/AGTC	0.00318978	0.0398085	intron-variant	CHD4	GRCh38.p7	12:6575301	AAAAATACAAAAATT[-/AGTC]AGGCATGGTGGTACA	1108
rs563520956	snp	C/G	0.00279162	0.0372561	intron-variant	CHD4	GRCh38.p7	12:6595173	ATCCTAGTGCTTTCT[C/G]ATATATAGAGATGTG	1108
rs563560501	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6606221	CCAGAGGAGTCACTC[A/G]GGAGAGCCCCAGATG	1108
rs563604896	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6580900	TAATCCCAGCTCCTC[A/G]GGAGGGTGAGGCAGG	1108
rs563660026	snp	A/C	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6587327	ATACCACCTTGGTCT[A/C]AATGCCAATTTTCAG	1108
rs563751676	snp	G/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6599470	TTTTAACAAAAAAAT[G/T]GAAAACATTGTAAGC	1108
rs563783252	snp	A/G	3.2987e-05	0.00406108	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581485	TTAAATTGTCCTCTC[A/G]TGCCTTTAAGAGCCA	1108
rs563876922	snp	A/G	0.00279162	0.0372561	intron-variant	CHD4	GRCh38.p7	12:6589493	CACATCATCGACTGG[A/G]CGTGGTGGCTCACGC	1108
rs564019103	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6594831	TTAGGGTCCTCCAGG[A/G]AACAGGGCTTAACCA	1108
rs564027550	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6574605	TTCTATGCAGATGAT[C/T]TGATGCTTCTCAAAC	1108
rs564074783	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6596597	CTGAGGTCGGGAGTT[C/T]AAGACCAGTCTGGCC	1108
rs564124009	snp	A/C/G	3.46568e-05	0.00416262	intron-variant	CHD4	GRCh38.p7	12:6601955	GAGGATGGAGGTCCA[A/C/G]GCACCTTTGAATCAT	1108
rs564166740	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6572016	CTGTAGTCCCAGCTA[C/T]TCAGGAGGCTGAGGC	1108
rs564266621	snp	C/G	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6603155	CCTAGGGGCCCGAAT[C/G]AGCCCAGCTGTCACC	1108
rs564295433	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6599584	CTGGCAAAACATCAA[C/T]TCCTCAGTTTGAAGT	1108
rs564295811	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575190	CAGTGGCTCACACTT[A/G]TAATCCCAGCACTTT	1108
rs564305030	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6604091	ACCAGCTTGGCCAAC[A/G]TGGTGAAACCCTGTC	1108
rs564364403	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606906	AACTCAGGTTCTCCT[C/G]AAGAGCTGCGGGGAC	1108
rs564369306	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6584107	AAATATTCAGAGAAA[A/C]AACAAAATTATGTCT	1108
rs564433562	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6597500	GAGCGTGGTGGCTCA[C/T]GCCTGTTAATCCTAG	1108
rs564494202	snp	A/T			upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570163	GGTTTTTTCCTTTTT[A/T]TTTTTTTCCACTTTA	1108
rs564694834	in-del	-/T	0.00517822	0.0506191	intron-variant	CHD4	GRCh38.p7	12:6585229	ATTCCTCACATACTA[-/T]TTTTTTTTACTATAA	1108
rs564751732	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6603845	CCAAATTTCTGATAC[A/C]CAAAAGATTTAGTTT	1108
rs564833985	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581914	TTCAAGCAATTCTCC[C/T]GCCTCAGCCTTCTGA	1108
rs564851160	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6584650	CAGCCTCCCAAAGTA[C/T]TGGGATTCTAGGCAT	1108
rs564874513	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6592136	GCCAACAACTGAGAT[C/T]TTTCTTCCAACACAT	1108
rs564948222	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6578339	TAAAGTCCCTGTACC[A/G]TGGTTTCTGACAAGA	1108
rs564984264	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6579074	AATCCCAGCATCTTG[A/G]GAGACAGCAGCAGGC	1108
rs565102071	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6597116	CTACTAAAAATACAA[A/G]AAAAAAAAAATTAGC	1108
rs565146222	snp	A/G			intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581506	TTAAGAGCCAGCCCT[A/G]TTCTTAGGACGGCCC	1108
rs565147793	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598603	ATCACGAGGTCAAGA[A/G]ATCGAGACCATCCTA	1108
rs565272981	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585529	CCTCGTGATCCACCC[A/G]CCTTGGCCTCCCAAA	1108
rs565301076	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605359	GGGGCTCTGAAAAAG[A/G]ACACAGAAGAGAAAG	1108
rs565330386	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6599309	GGATGTGGTGGCATG[C/T]ACCAGTACTCCTAGC	1108
rs565430129	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6599583	GCTGGCAAAACATCA[A/G]CTCCTCAGTTTGAAG	1108
rs565608066	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6605182	GAAGCTAAGAAGAGA[A/G]AAGGCAGAAGTGAAT	1108
rs565763009	snp	A/G			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581629	AGAGGGACAGAAAAT[A/G]ATAGGACAGGCAGAC	1108
rs565798602	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6594258	TGCCCTCAAATCTTC[A/C]GCTGTGTACATGTGT	1108
rs565957290	snp	C/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6575600	ATTTTCCACAACCAG[C/G]ATCACAGCCCAGACC	1108
rs566062997	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6574542	CATATGACTCAACAT[A/G]AGAGAAGATTTCTCA	1108
rs566100817	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6591323	CAATACATTCGTCCA[A/G]TTGAGACATTCAAAA	1108
rs566149129	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581898	GTCTCCGCCTCCCGG[C/G]TTCAAGCAATTCTCC	1108
rs566163437	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6595487	CTATAGAAGAAACAA[C/T]TTGGCCAGGCACAGT	1108
rs566170562	snp	A/G	0.000265644	0.0115218	synonymous-codon, intron-variant	CHD4	GRCh38.p7	12:6602167	CAGCTGCCGGCATAA[A/G]AGCATACGCTGGAGC	1108
rs566175404	snp	C/T	0.000399281	0.0141238	splice-acceptor-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606452	CACTGGCCCGAGTCA[C/T]TGTGCGGGGGAGGGG	1108
rs566196712	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6587634	GCAAGTCCCACAAGA[A/C]CCTTGGTATCAAAGA	1108
rs566274542	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575963	CAAAAAAATCTCCGT[C/T]GCATTCTTCAAAACT	1108
rs566549059	snp	A/G	0.00199481	0.0315187	intron-variant	CHD4	GRCh38.p7	12:6603350	ATTCACACTGGCTCC[A/G]ACTCCCTCCTCCCTC	1108
rs566549169	snp	G/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6596877	AGGCAGAGAATCACT[G/T]GAGCCTGAGAGGCGG	1108
rs566585336	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597155	GTGGCGATGGCCTGT[A/T]GTCCCAGCTACTCGG	1108
rs566636723	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607013	GGGGCCGGGCCACGT[A/G]TCCCGGGGGGCAAGT	1108
rs566751935	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595585	CTGAGGTCAGGAGAT[A/C]GAGACCAGCCTGGTC	1108
rs566856492	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602606	TCTTGTCCCAGATTC[C/T]TCTGAAGAGAACTGC	1108
rs567050827	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608718	ACCATCATTTCCAGA[C/T]ACTCGGGGGCTGGGA	1108
rs567244191	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604170	ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAGGAG	1108
rs567253385	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571934	CCATTGCTCTCCAGC[C/T]TGGGCAACAAGAGCA	1108
rs567329783	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6584338	AACATTAGTTGTCCC[C/T]AAGAAGGGAACTAAA	1108
rs567391357	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604725	CAAACCGCAAACTTA[C/G]TGAGATATAGAGAAG	1108
rs567426939	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6573028	ATTAGGATGCAGTCA[C/G]ATCAGGGAGGCCGAA	1108
rs567535545	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6577698	AAGTGAGAACAGTGC[A/G]CTGGATGGACAGACT	1108
rs567571806	snp	C/G	0.00318978	0.0398085	intron-variant	CHD4	GRCh38.p7	12:6571401	CTTTTACTTTAATTA[C/G]AAACAAAATGTTGAA	1108
rs567609607	snp	A/G	9.89511e-05	0.00703319	missense	CHD4	GRCh38.p7	12:6578453	ATGAAACGTTGTTTA[A/G]TATTTTTCTTCTGTT	1108
rs567632675	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6586184	TGGGTGGATCACAAG[A/G]TCAGGAGATCGAGAC	1108
rs567718143	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6579852	ACGAGGTCAGGAGGT[A/G]GAGACCATCCTAGCT	1108
rs567737335	snp	A/C/G	0.000319038	0.0126262	intron-variant	CHD4	GRCh38.p7	12:6600447	AAAACTACCTCCCCC[A/C/G]ACCCCCCGACCCCTA	1108
rs567737597	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6579463	GTGGCGCATGCCTGT[-/A]ATCCCAGCTACTCAG	1108
rs567741400	snp	A/C	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6594299	TCACATTTATCTACT[A/C]TCTACTAAACACATG	1108
rs567790049	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6576646	GAGTCTCGCTCTGTC[A/G]CCAGACTGGAGTGCA	1108
rs567879649	snp	A/G	4.95225e-05	0.00497582	missense	CHD4	GRCh38.p7	12:6598322	GGCTTTGGGGAGGGC[A/G]TGTTGGGATCAGCAT	1108
rs567907186	snp	A/G	0.00279162	0.0372561	intron-variant	CHD4	GRCh38.p7	12:6573510	TCTTATACAAAAGCG[A/G]TAAAAACTCAATTTA	1108
rs567911348	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6585714	GAACTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC	1108
rs567914709	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6592929	ATCCCACTCCTCACA[C/T]TCTTTTTAAAGGCCT	1108
rs568006107	snp	A/G	0.000399281	0.0141238	missense	CHD4	GRCh38.p7	12:6593535	CGACATACATGTCTG[A/G]AGCCCACATTTCAAA	1108
rs568191723	snp	G/T			synonymous-codon	CHD4	GRCh38.p7	12:6598354	TGGAGGCCGAGGCAC[G/T]GGTGTGGGAGATGGT	1108
rs568212236	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6596230	GTTTGTTTCACACCA[G/T]ACCTCTAGGTATGCC	1108
rs568261896	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597308	AAATAAATAAAGATA[A/G]TAACATGAAGTGTCA	1108
rs568337439	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605925	AATCCTCAACGCCCC[C/T]CTCCACCACCACCAC	1108
rs568449840	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607085	CCAAGCCGGAGGCGG[A/G]GGGTCGCGGGGAGCA	1108
rs568497750	snp	C/T	0.000188791	0.0097139	synonymous-codon	CHD4	GRCh38.p7	12:6602050	TCCAAGCTTCTTCTT[C/T]TTCTTCTTGCCAGGA	1108
rs568539498	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6601592	AAAAGAAAGAGAAGT[A/G]AGAAGAGAGAACAGA	1108
rs568544844	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6588566	GTGGATCATTTGACA[G/T]CAGGAGTTCGAGACC	1108
rs568613560	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570389	CAGGAACCCACAACA[A/G]TTTGTGTGTAACAGG	1108
rs568624167	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6595720	TTGAACCCAGGAGGC[A/G]GAGGCTGCAGCGAGC	1108
rs568631475	snp	A/G	5.10035e-05	0.00504967	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581703	CCCCTGGAGTGGAGG[A/G]TGTAGGAGTTTTTGG	1108
rs568745135	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583573	AATTACATATAGATT[A/T]GCAGTCAGCATAACT	1108
rs568749721	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6605056	CCAACAGCCCAGACT[C/T]CATGACAACACTAAC	1108
rs568759908	snp	C/T			synonymous-codon	CHD4	GRCh38.p7	12:6591979	ATCCATCACCACATT[C/T]AGCAGAGACACCTGG	1108
rs568824799	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576669	GGAGTGCAGTGGTGC[C/G]ATCTCGGCTCACTGC	1108
rs568935100	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6590983	CAAAAATTAGCTGGG[C/T]GTGGTGGCACACGCC	1108
rs569096822	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596289	TGTACCAGTCTCTGA[C/T]CAAAAATTATCTCTA	1108
rs569100347	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	CHD4	GRCh38.p7	12:6570950	TAACCTCACAGCAAC[C/T]GGGGGAATTCGGGCA	1108
rs569133318	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6589621	ACAGTACAAAAATTA[C/G]CCGGGCGTGGTGGCG	1108
rs569222794	snp	A/C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6590223	AAAAATCTGTATCAT[A/C/G]TAAGAAAATAAAGAA	1108
rs569400060	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608775	ACCAAAATCTAGGTA[C/T]TTTCCAGATGCTTAC	1108
rs569448098	snp	C/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6603434	GAGTGGAGAGAAGAA[C/G]GGAGTGCCTCACCCA	1108
rs569486289	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597260	CAGCCTGGGTGACAA[C/G]TCTGTCTCAAAAAAA	1108
rs569570115	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604020	CAATGGCTCATGCCT[A/G]TAATCGCAGCACTCT	1108
rs569727743	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6578617	CCTTACCCAGAACAC[C/T]GTATGCTACAAGAAT	1108
rs569896454	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6579107	ATCACTTGAGGTCAG[A/G]AGTTCAAGACCAGCC	1108
rs569936128	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572512	GAGGCCGGAGGATCA[C/T]TTGAATCCAGGAGTT	1108
rs570052770	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6574475	AAGAGGCAGAATGTT[C/G]GTTCTTAATTTATGA	1108
rs570125852	snp	C/T	1.66874e-05	0.0028885	intron-variant	CHD4	GRCh38.p7	12:6587980	AAATAAAGCCAGAAA[C/T]TGTATTTTCCTGGTG	1108
rs570278296	snp	C/T	0.000173193	0.00930412	intron-variant	CHD4	GRCh38.p7	12:6593659	CTGAGGGCCCCAGCA[C/T]ACTGCAACCCCAGCG	1108
rs570302670	snp	C/T	0.00636936	0.0560724	intron-variant	CHD4	GRCh38.p7	12:6579928	GGGCATGGTGGCAGG[C/T]GCCTGTAGTCCCAGC	1108
rs570314617	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6586294	AGTCCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA	1108
rs570367962	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595508	CAGGCACAGTGGCTC[A/T]CACCTGTAATCCCAG	1108
rs570410555	snp	C/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6586829	CAGCCTCCCGAACAC[C/G]TGGGACTACAGGTGT	1108
rs570480557	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608206	CACATCACCCCCAGC[A/C]TTCCCTCTTCTAGCT	1108
rs570518542	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608603	GCTACCCACGCTTCC[C/T]TGTCCCCGCCCCCAC	1108
rs570600730	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6602569	GGCCCTAATCCAGAG[A/G]CTTTAGACTTTATTC	1108
rs570628234	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605981	CCTGCATTCCTCCGA[A/G]GACCCACATACCAGG	1108
rs570630078	snp	A/T	1.76521e-05	0.00297081	intron-variant	CHD4	GRCh38.p7	12:6601070	TAAAATCAGGATATA[A/T]CCAAATATATACCAC	1108
rs570713882	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6600462	CACCCCCCGACCCCT[A/T]TCTCCTTAGGGAGAT	1108
rs570767790	snp	C/T	1.78761e-05	0.00298961	intron-variant	CHD4	GRCh38.p7	12:6598453	GAGACAACTTAATCT[C/T]AAATCATAACCATGG	1108
rs570774016	snp	A/G			utr-variant-3-prime	CHD4	GRCh38.p7	12:6570588	AGAAGGAAGGTGAGG[A/G]TCTCTCAGGCCCCCA	1108
rs571012408	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575362	CTGAGGCAGGAGAAT[C/T]GGTTGAAGCCAGGAG	1108
rs571079796	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6591147	AAAAAAAAAAAAAAA[A/C]AAAACCTAGTAGCGT	1108
rs571249742	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6577525	CCTGAATACTCCAAT[C/G]TGCAGTGTTCCCCAA	1108
rs571323074	snp	C/T	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6585081	GATGACAAAGACCAC[C/T]AGAACCAATGCCAAC	1108
rs571332480	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6571912	ATTGTGGTGAACTGA[C/G]ATCGCGCCATTGCTC	1108
rs571341716	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	CHD4	GRCh38.p7	12:6609332	TTATCGTGGTCCTTC[C/T]AGAGGCTGGAAGATG	1108
rs571416337	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608568	CTATTCTAACACCCA[C/G]AGCAGGGAGGGCCAG	1108
rs571454698	snp	C/T	0.323908	0.238825	intron-variant	CHD4	GRCh38.p7	12:6579177	AAAATTAGCTGGGTG[C/T]GGTGGCTCATGCCTG	1108
rs571556181	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604963	CCCTTACCAGCACCA[C/T]AACTCCGCCCTCACC	1108
rs571565617	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576741	TTATGCCAATCAGCA[A/G]TCTCTCTCCTGATAT	1108
rs571608092	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6584302	ATAAAATATTTTTGG[A/G]AAGATATAAAAGGAA	1108
rs571629969	snp	C/T	0.000399281	0.0141238	synonymous-codon	CHD4	GRCh38.p7	12:6592776	TGTCCCAGTCAGCAA[C/T]AGCTTGTGCTGGAGT	1108
rs571673530	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598544	GACCTGGAGCAGTGG[C/G]TCATGCCTGAAATCC	1108
rs571716589	in-del	-/T	0.378372	0.214524	intron-variant	CHD4	GRCh38.p7	12:6576942	GACAACAGACACGTC[-/T]TTTTTTTTTTTTGAG	1108
rs571840094	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597736	ACGCCACTGCACTCC[A/G]GCCTGGGCACAGAGT	1108
rs571876753	snp	A/G	0.000131789	0.00811648	intron-variant	CHD4	GRCh38.p7	12:6591664	GGGTTGTCTATGACT[A/G]TTCCCTAAAGCTCCC	1108
rs571991355	in-del	-/ATG			intron-variant	CHD4	GRCh38.p7	12:6574196	TTTCTAAGTTACAGA[-/ATG]ATGTTTTCTGTATCT	1108
rs571991906	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6575365	AGGCAGGAGAATCGG[C/T]TGAAGCCAGGAGGCA	1108
rs572033484	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580894	TGTCTGTAATCCCAG[C/T]TCCTCGGGAGGGTGA	1108
rs572053071	snp	A/G			synonymous-codon	CHD4	GRCh38.p7	12:6606278	GAAGATGTTACCTGG[A/G]TGGGGTGGGGGCAGG	1108
rs572076697	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6586380	CACTCCAGCCTGGGG[A/G]AGAGAGTGAGATTCC	1108
rs572163642	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6585873	GAGGCCGAGGCAGGC[A/G]GATCACTTGAGGTCA	1108
rs572246464	snp	A/C/G/T	8.24107e-05	0.00641874	synonymous-codon	CHD4	GRCh38.p7	12:6597929	GATCATCATCCACTC[A/C/G/T]GGTTTTATCCCATAG	1108
rs572283142	snp	A/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6592151	CTTTCTTCCAACACA[A/T]CCCACTTTGGAACTA	1108
rs572372291	snp	C/T			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569605	AGAAGGGGTGAACTA[C/T]AAGGGTTTCAAGGTT	1108
rs572445979	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6605653	GCCCCTCTTCACTAG[A/G]CTATTACATCCTCCC	1108
rs572478415	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6599335	CTAGCTACTCAGCAA[A/G]AGGTTGAGATAGGAG	1108
rs572483767	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6606121	CCCCCTCACACCAGA[C/G]CTCCGCAGAAGGGAA	1108
rs572486417	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6574920	ATGGCTCAAGAGCTA[A/G]GAATGGGTTTTACAT	1108
rs572536563	snp	C/T	0.000190726	0.00976352	intron-variant	CHD4	GRCh38.p7	12:6594443	ACAAAAAACTATCCA[C/T]CCCAGATTTCCTTAC	1108
rs572567744	snp	A/G	0.000347041	0.0131682	intron-variant	CHD4	GRCh38.p7	12:6600017	CCTTCCTTCTCCTGC[A/G]GTAAAGGACCACAGA	1108
rs572570864	snp	A/G	0.00199481	0.0315187	intron-variant	CHD4	GRCh38.p7	12:6572724	TGCGCCACATGCCCA[A/G]CTAATTTTTCTATTT	1108
rs572583477	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6597339	GGCGCAGTAGCTCAC[A/G]CCTGTAATCCTAACA	1108
rs572594695	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6599130	TAAAGCAGTAAGTGG[C/T]CCTATTAAACATTCT	1108
rs572605696	in-del	-/AG	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6577709	GTGCGCTGGATGGAC[-/AG]ACTCCCTCTGCTGCA	1108
rs572734539	snp	C/G	0.000708314	0.0188057	synonymous-codon	CHD4	GRCh38.p7	12:6573177	AGCAAAGCGGGTGTT[C/G]AGGGCCATGGAAGGG	1108
rs572748479	in-del	-/CA			intron-variant	CHD4	GRCh38.p7	12:6584954	GTCAGACCATTCAGC[-/CA]CACTTACATATAAAC	1108
rs572758733	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580564	AATACAAAATTAGCT[A/G]AGCATGGTGGTACAT	1108
rs572882041	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606575	CACCCGAACCGCTCA[A/G]GCTGAACTTAGTTCC	1108
rs573194448	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595873	TAAGGCAGGAGAATC[A/G]TTTGAACCAGGAAGT	1108
rs573196276	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602237	ACACACATGCTGACC[C/T]CAGGACAGCCCTGAG	1108
rs573233001	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596478	AACATGGCGAAACCC[A/G]TCTCTACTAAAAAAA	1108
rs573331385	snp	A/G			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607621	CGCGTCACCTGGGCA[A/G]CCGCCCACCTCCTGG	1108
rs573332229	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6583844	CAACTGTCTGCAGAA[C/T]GAAAAGAATTCTATA	1108
rs573417503	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576282	AAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC	1108
rs573419199	in-del	-/C	0.00159617	0.0282053	upstream-variant-2KB	CHD4	GRCh38.p7	12:6607732	CACACACACACCCTG[-/C]CCCCCCCACATTTCA	1108
rs573487283	snp	A/G	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6577030	AAATCTCTACCTCCC[A/G]ACTTCAAGCGATTCT	1108
rs573514374	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6589210	ATGTCAGAATATAAA[A/C]CCTCATTAGGCAAAC	1108
rs573654042	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602936	GAATATACCTTCCCA[C/G]AACAGGATCAGTTCA	1108
rs573684472	in-del	-/A/AA	0.0779505	0.181391	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581016	TCAAAACAAACAAAC[-/A/AA]AAACAAAAAAAATGT	1108
rs573687462	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6591161	AAAAAACCTAGTAGC[A/G]TCTACTGAGGCAGAC	1108
rs573690817	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597007	GAGTGCGGCGGCTCA[C/T]GCCTGTAATCCCAGC	1108
rs573691154	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6603699	AAACCCAAGGAAAGC[A/G]AGACAAACATGAAGG	1108
rs573763646	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572665	GGGTTCCAAGCGATT[C/T]TCCTGCCTCAGCCTC	1108
rs573779681	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6597331	AAGTGTCAGGCGCAG[C/T]AGCTCACGCCTGTAA	1108
rs573836213	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608917	TCCCATCCAAAGACT[A/C]TCTCTCAACATTCTA	1108
rs573859767	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576924	ATTATACTCAGCGTA[C/T]GAGACAACAGACACG	1108
rs573861466	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569985	TCAGTGGGGTATCAG[C/G]ACACCACGTAGCCCT	1108
rs573952463	snp	A/G	8.24137e-05	0.00641873	intron-variant	CHD4	GRCh38.p7	12:6570700	CTGGGCTACCTAGAG[A/G]AGGAGACCCGAGGAG	1108
rs573997532	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6570784	GCCACCCACCCAGTA[C/T]GTAAAGCTAGGGACA	1108
rs574033463	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6604349	CCCCAAAATTAGCCC[C/T]AAAATGTCTCTGGCT	1108
rs574303747	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598571	ATCCCAGCACCTTGG[G/T]AGGCCGAGGCGGGCA	1108
rs574389718	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6598994	CTGGACATCGTCCAG[A/G]ATTTGCGTGCCACCA	1108
rs574391592	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6593286	GTGTAAGCACAACCA[A/G]GAGACTGATGGAATG	1108
rs574397198	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6586499	GGAGGTCAAGGCAGG[A/G]GAACTGCTTAAGGCC	1108
rs574434073	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580134	TCAGAGGCTGAGGCA[A/G]GAGAATCGCTTGAAC	1108
rs574494426	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6580460	GCCTGTAATCCCAGC[A/G]CCTTGAGAGGCCAAG	1108
rs574496581	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6594885	CACTGAGGAAAAGCA[C/T]GTCACAGACTCCCTA	1108
rs574625930	snp	C/T	5.51354e-05	0.00525021	intron-variant	CHD4	GRCh38.p7	12:6573300	GAGGAAACGGGAGTT[C/T]GACTGATAACTCACT	1108
rs574647733	snp	A/G	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6593939	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	1108
rs574819772	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6589277	CGAATACTAATATCG[A/G]TGTGAAAGTTTAAGG	1108
rs574834214	snp	G/T	0.0107246	0.0724382	intron-variant	CHD4	GRCh38.p7	12:6575512	GGGAGAAAAAAAGGT[G/T]TGCTGACCCCTACAG	1108
rs574896161	snp	C/T	1.76633e-05	0.00297176	intron-variant	CHD4	GRCh38.p7	12:6594702	GAACTCCCCTCCTCC[C/T]CTAATAGAGCAGCTG	1108
rs574983460	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6595125	TCAAAATATACCTCC[C/T]TTTTTTTTTTCTGAT	1108
rs575058640	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6588871	AATCACTTGAGCCCA[A/G]GAGTTCAAGGTTATA	1108
rs575061804	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6606212	CCTGCCTCACCAGAG[A/G]AGTCACTCGGGAGAG	1108
rs575064684	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6573979	AGTGAGCCAGGATCG[C/T]GCCACTACACTCCAG	1108
rs575154781	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6576044	CTCCAATTCCCTCTC[A/G]AGAACTTTTTTTTTT	1108
rs575181292	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6585344	GGCTGGAGTGCAGTG[C/G]GGCAATCTTGGCTCA	1108
rs575228059	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608397	ATAATAATTGCAAGG[A/G]GCCCGTGGTCAACCA	1108
rs575434974	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596525	AGGCATCAGGCCGGG[C/G]GCGGTGGCTCACGCC	1108
rs575446849	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575059	TAACTTATTCATTTA[C/T]GTATCCCCTGTGGCT	1108
rs575489537	snp	C/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6575584	TATCTTTACCCTTTT[C/G]ATTTTCCACAACCAG	1108
rs575520824	snp	C/T	0.00159617	0.0282053	intron-variant	CHD4	GRCh38.p7	12:6590042	TGTCTCTACTAAAAA[C/T]ACAAAAATCTGGGCC	1108
rs575568519	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6590448	AGCTAGTTGAACAGT[A/G]TACATGAACTCTCTC	1108
rs575600343	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6576952	ACGTCTTTTTTTTTT[C/T]TTGAGACAGAGTCTC	1108
rs575654861	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6584383	GAGAGAAAAGAGATA[C/T]GTGTGTGTACATATA	1108
rs575714918	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602267	GGCTCATCCCCAGAA[C/T]ATGGCCCACCACTTC	1108
rs575846387	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6570815	TACAGCAAAGTTACA[A/G]GCTCCAGAATGGTTC	1108
rs575912025	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB	CHD4	GRCh38.p7	12:6609303	TTCCAAGAGAGAACA[C/T]ATCCCAATAAGATTT	1108
rs575919767	snp	C/G	0.000287689	0.0119901	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582983	AGGTAGGATATTAAA[C/G]AAAGCAACATTTAGA	1108
rs575956834	snp	G/T	0.0023933	0.0345097	intron-variant	CHD4	GRCh38.p7	12:6604248	CACTGCACTCCAACC[G/T]TGGCGACAGAGTGAG	1108
rs575968437	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6585827	AAGAGGCCAGGCGTA[A/G]TGGCTCATGCCTGTA	1108
rs575993184	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6602956	GGATCAGTTCAGGGG[C/T]CTCGGAAACCACACC	1108
rs576279993	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6571498	TGTATTATTCTGCTT[C/T]GCTTTCCATCTCAAG	1108
rs576333940	snp	A/G	0.000197873	0.00994471	intron-variant	CHD4	GRCh38.p7	12:6573046	CAGGGAGGCCGAATC[A/G]GCAGGAGGCAGGGGA	1108
rs576396714	snp	A/G	0.00199481	0.0315187	intron-variant	CHD4	GRCh38.p7	12:6605170	TCAACTTCCACTGAA[A/G]CTAAGAAGAGAGAAG	1108
rs576584900	snp	C/T	0.327445	0.237702	intron-variant	CHD4	GRCh38.p7	12:6579069	CCTGTAATCCCAGCA[C/T]CTTGGGAGACAGCAG	1108
rs576716023	snp	G/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6586566	ATCTCTAAAAACATT[G/T]AAAAAATTAACCAGG	1108
rs576723445	snp	C/T	0.0023933	0.0345097	intron-variant	CHD4	GRCh38.p7	12:6585767	GCACTCCAGCCTGGG[C/T]GGGAAAGCAAGACTC	1108
rs576833890	snp	A/G	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6574029	CTGTCTCAAAAAAAA[A/G]GGGGTTATTTTGCTA	1108
rs576931389	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6599258	GCAACATAGTGAGAC[C/T]CTGTCTCAACAGAGA	1108
rs576946597	in-del	-/A	0.188316	0.242271	intron-variant	CHD4	GRCh38.p7	12:6579751	GTAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	1108
rs576969005	snp	C/T	0.00557542	0.0525036	intron-variant	CHD4	GRCh38.p7	12:6594005	CACATCCGGCTAATT[C/T]TGTATTTTTAGTAGA	1108
rs577051697	snp	A/G	0.00119737	0.0244387	intron-variant	CHD4	GRCh38.p7	12:6594358	TGTTCTTGAAGGTCA[A/G]AGACCAATTTTTTTA	1108
rs577060713	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606495	AACAGTCAGTGACGC[C/G]CACTGTCCCCCTCCC	1108
rs577096838	snp	C/T	0.00279162	0.0372561	utr-variant-5-prime, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607403	CTCCGGCTCCAGCGT[C/T]GCCTCTTAAAGGGCC	1108
rs577137374	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6595175	CCTAGTGCTTTCTGA[C/T]ATATAGAGATGTGGA	1108
rs577440353	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6589679	GGCTGAGGCAGCAGA[A/C]TGGCTTGAACCCGGG	1108
rs577551370	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570532	CTCCCTCCCCTCCCC[C/G]AGTGCACTGGGGCTG	1108
rs577636738	snp	C/T	0.000798403	0.0199641	intron-variant	CHD4	GRCh38.p7	12:6577971	GTAAGAACCTCAAAC[C/T]AAAAGACCTTCAGAA	1108
rs577664649	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CHD4	GRCh38.p7	12:6608462	CACATCCCATAATGC[C/T]TCATCTCCACTCTAC	1108
rs577673920	snp	C/T	3.3e-05	0.00406189	missense	CHD4	GRCh38.p7	12:6578851	AAACACCCACCTTTG[C/T]CTTCTACCACAATAG	1108
rs577699004	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6577295	GGTGTGGTGGCAGGC[A/G]CCTGTAATCTCAGCT	1108
rs577753127	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602301	GAAAGAAACAAATGC[C/T]CTCAGCCCTTCAACC	1108
rs577792234	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6602847	AGATTTAGGCCTCCT[A/G]TAACTGGCCACCAAG	1108
rs577801372	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6602851	TTAGGCCTCCTGTAA[C/T]TGGCCACCAAGTTAT	1108
rs577910095	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6584093	CAACCATAGATGGAA[A/G]ATATTCAGAGAAAAA	1108
rs578082754	snp	C/T	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6572074	GAGGTTGCAGTGAGC[C/T]GAGATCACGCCATTG	1108
rs578085343	snp	A/G	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6596992	ATAAATAAATAGGCC[A/G]AGTGCGGCGGCTCAC	1108
rs578190338	snp	A/C	0.000399281	0.0141238	intron-variant	CHD4	GRCh38.p7	12:6591077	GCAGTGAGCCAAGAT[A/C]GTGCCGCTGCACTCC	1108
rs745342482	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6585974	GCATGGTGGTGCATA[C/T]CTGTAATCTCAGCTA	1108
rs745351452	snp	A/C/G	4.9728e-05	0.00498618	intron-variant	CHD4	GRCh38.p7	12:6602191	CTGGAGCAGGGCAAG[A/C/G]GGGGAAGAGGGAGAC	1108
rs745353327	snp	A/G	1.64735e-05	0.00286993	missense	CHD4	GRCh38.p7	12:6595365	TCTGGAGGCCTCTCC[A/G]ACTTCCGAAGCTTCA	1108
rs745406197	snp	A/G	3.33139e-05	0.00408116	intron-variant	CHD4	GRCh38.p7	12:6578141	GGGAGTGCAACTCTG[A/G]GGAGGAATTTAGGGA	1108
rs745414096	in-del	-/TCT	5.20892e-05	0.00510313	cds-indel, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581742	ACCCTGGCTGGGACA[-/TCT]TCTTGTTTTCCTCCA	1108
rs745467712	snp	C/T	1.6522e-05	0.00287414	missense	CHD4	GRCh38.p7	12:6598059	TCCATATCATTCTTC[C/T]GCTGATAGTTTCGGA	1108
rs745481056	snp	C/T	1.65943e-05	0.00288043	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582927	CCCTTACGACTGGGC[C/T]TACGGGGAGCTGCAA	1108
rs745540978	snp	A/C	1.65209e-05	0.00287405	missense	CHD4	GRCh38.p7	12:6600635	ATACTGGCATCATCG[A/C]AGTCAGATTCCACAT	1108
rs745553945	snp	A/G	1.64765e-05	0.00287019	intron-variant	CHD4	GRCh38.p7	12:6591862	AAAGTATTAAAAGAA[A/G]GCCCACATGGAGAAG	1108
rs745561896	snp	C/G	9.88386e-05	0.00702919	intron-variant	CHD4	GRCh38.p7	12:6602363	TCCCCGTAACATTCA[C/G]TCACCCACTCACCTC	1108
rs745566542	snp	C/T	3.32165e-05	0.00407519	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582793	CAGCAGGTCGCATTC[C/T]ACCAAAGATGCAATA	1108
rs745567119	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6585141	GAGGACAAGAAAAAG[G/T]AAATTTTATTTTTCC	1108
rs745588000	snp	A/G			upstream-variant-2KB	CHD4	GRCh38.p7	12:6609383	TATAGACCATAGTCA[A/G]CATGATCTCCTATCT	1108
rs745589253	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6575800	CCCGTCCACCTTTCT[C/T]GTTCCAACCTACCTC	1108
rs745607267	snp	C/T	1.71622e-05	0.0029293	missense	CHD4	GRCh38.p7	12:6606364	ACGGGGAGCCCAGGC[C/T]CGACGCCATCCCCTT	1108
rs745643323	in-del	-/AGAC	3.45477e-05	0.00415604	intron-variant	CHD4	GRCh38.p7	12:6601914	GTCTAGGAAACAAAA[-/AGAC]AAAAGTTTAACAGTA	1108
rs745656901	snp	C/G	1.65422e-05	0.0028759	intron-variant	CHD4	GRCh38.p7	12:6598180	TTTTGTCACTATCCT[C/G]TTCATCGTAGCCCCT	1108
rs745745173	snp	A/G	1.66527e-05	0.00288549	intron-variant	CHD4	GRCh38.p7	12:6587969	AGTTGAACAGGAAAT[A/G]AAGCCAGAAATTGTA	1108
rs745772053	snp	A/C	1.73589e-05	0.00294604	intron-variant	CHD4	GRCh38.p7	12:6573283	AGCTGGACAAGGGAT[A/C]AGAGGAAACGGGAGT	1108
rs745807711	snp	C/G	9.88517e-05	0.00702966	intron-variant	CHD4	GRCh38.p7	12:6601623	AAGATTCTCCTCCCC[C/G]TTCCCCAAACCCCTT	1108
rs745832915	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6590544	AGTAGTGATACTGAG[C/T]ACAGTGGCTTATGCC	1108
rs745850899	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6603156	CTAGGGGCCCGAATC[-/A]GCCCAGCTGTCACCA	1108
rs745855056	snp	A/G	1.64795e-05	0.00287045	synonymous-codon	CHD4	GRCh38.p7	12:6593467	ATTGTCTTCAAAGGA[A/G]AACTCATTCTCTCGG	1108
rs745862017	snp	G/T	3.29587e-05	0.00405934	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581205	AACAAAAACAAAACA[G/T]ATGAAGCAGACAGGC	1108
rs745876689	in-del	-/T	9.92228e-05	0.00704284	intron-variant	CHD4	GRCh38.p7	12:6599741	GACTACACTTTCCCA[-/T]TTTTTTGCCCCGGCT	1108
rs745877775	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6601183	CCAAGACTCATTCCT[C/T]CCTCCTATCTCCTAC	1108
rs745886583	snp	C/T	1.6476e-05	0.00287014	synonymous-codon	CHD4	GRCh38.p7	12:6573144	GTGCTGATGACTTTC[C/T]GCCAAACACTCCACC	1108
rs745929513	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6585370	GCTCACTGCAAGCTC[A/T]GCCTCCCAGGTACAA	1108
rs745941658	snp	A/G	1.77087e-05	0.00297557	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581765	TTTTCCTCCACCTCA[A/G]CCAGTTCAGGCATGC	1108
rs745942514	in-del	-/CAAAC	1.65575e-05	0.00287724	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581016	CTCAAAACAAACAAA[-/CAAAC]AAAAAAAATGTGGAT	1108
rs745966223	snp	C/T	1.65908e-05	0.00288012	missense	CHD4	GRCh38.p7	12:6588416	CAGAACTGCTGAGCA[C/T]CCGGTGCTAATAAAA	1108
rs745992315	snp	A/G			intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607168	GGGCCAGGAAAGGAA[A/G]GGTCGGCTCCTCTGG	1108
rs746008542	snp	C/T	1.64904e-05	0.00287139	missense	CHD4	GRCh38.p7	12:6596118	TGATCAAGTAGTGGA[C/T]GTGGCCCTTCTTGTC	1108
rs746023710	snp	A/C	5.00847e-05	0.00500398	intron-variant	CHD4	GRCh38.p7	12:6592095	CAGGTTAGACTTGAG[A/C]GCCTTTCAATGACTA	1108
rs746108222	snp	A/G	3.29462e-05	0.00405857	synonymous-codon	CHD4	GRCh38.p7	12:6599800	ACAGAGCCATTCACC[A/G]TTGGGGATCTCTGGA	1108
rs746112629	snp	C/T	1.64866e-05	0.00287106	missense, intron-variant	CHD4	GRCh38.p7	12:6600375	TCTCATAACCATCCA[C/T]AGCAGTCACCTCCTC	1108
rs746125290	in-del	-/TGAG			intron-variant	CHD4	GRCh38.p7	12:6575432	TCCAGCCTGGGCAAC[-/TGAG]TAAGACTTTGTCTCA	1108
rs746126059	snp	A/C	1.6906e-05	0.00290736	intron-variant	CHD4	GRCh38.p7	12:6595965	CCATCTCAAAAAAAA[A/C]AAAAAAGAAACAACT	1108
rs746129305	in-del	-/AGGCA	1.64931e-05	0.00287163	intron-variant	CHD4	GRCh38.p7	12:6573052	GGCCGAATCGGCAGG[-/AGGCA]GGGGAGCCACTGGCT	1108
rs746196724	snp	A/G	5.24278e-05	0.00511969	intron-variant	CHD4	GRCh38.p7	12:6601056	CGAGCATTGGGACCT[A/G]AAATCAGGATATATC	1108
rs746260416	snp	A/G	1.64901e-05	0.00287137	intron-variant	CHD4	GRCh38.p7	12:6570730	GTCAGAATTCCAGAT[A/G]ATAGGAATCCACCCA	1108
rs746260563	snp	C/G	1.64953e-05	0.00287182	missense	CHD4	GRCh38.p7	12:6578892	TATTGCTGACTTTTC[C/G]TCCACCTTCTCTACA	1108
rs746279263	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6571341	CTCCCCACCTCCATT[A/G]TAACAGCATTCTTTT	1108
rs746282447	snp	C/T	1.64762e-05	0.00287016	missense	CHD4	GRCh38.p7	12:6602473	TCTGTTTCTGACAAA[C/T]CCTCTTCTGGGTCCT	1108
rs746335183	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	CHD4	GRCh38.p7	12:6587441	TGAGCTCAAATATTC[A/G]TTCATGCCCTGCAAT	1108
rs746346870	snp	A/G	3.29625e-05	0.00405958	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581425	TCAATTAGGAAGAAG[A/G]TACTAGATCAGAGAG	1108
rs746355798	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6605413	CAACCATCATTTGAG[A/G]ATAGACAACAGTTCC	1108
rs746400780	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6572427	TAGACTCTATCTCAG[-/A]AAAAAAAAAAAAAAA	1108
rs746420431	snp	C/G	1.6615e-05	0.00288223	intron-variant	CHD4	GRCh38.p7	12:6601266	CACTAGACACCCCCA[C/G]TCCCATTTGAACCCC	1108
rs746423034	snp	C/G	1.64749e-05	0.00287005	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583289	ATCTTCTTGCTGCTG[C/G]TCATAATGGTGCCGC	1108
rs746465024	in-del	-/AAAA	1.64789e-05	0.0028704	intron-variant	CHD4	GRCh38.p7	12:6591855	AAAGAAAAAAGTATT[-/AAAA]GAAAGCCCACATGGA	1108
rs746470142	snp	A/G	1.79046e-05	0.00299199	intron-variant	CHD4	GRCh38.p7	12:6600889	TCCTTTCTATTAGAC[A/G]TGGCACCCTCCCTAA	1108
rs746492700	snp	C/T	3.32364e-05	0.00407641	synonymous-codon	CHD4	GRCh38.p7	12:6592054	GATGTACTTGTAGTA[C/T]TTCCTACATGGGCAA	1108
rs746495843	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6605791	CAGCACAGAAAACCG[A/G]TAACCGATCAGAAGC	1108
rs746525996	snp	A/G	1.66228e-05	0.0028829	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582953	TGCAAGAAGAAAAAG[A/G]TGAATGAGTGACACA	1108
rs746573192	snp	C/T	1.64732e-05	0.0028699	missense	CHD4	GRCh38.p7	12:6602378	GTCACCCACTCACCT[C/T]CTTTTTTTGGCGCTT	1108
rs746594662	snp	A/C	1.64765e-05	0.00287019	missense	CHD4	GRCh38.p7	12:6593499	TGATGGCACGGCTGT[A/C]CTTGTCACCCACATA	1108
rs746604364	snp	C/T	3.30158e-05	0.00406286	synonymous-codon	CHD4	GRCh38.p7	12:6598321	GGGCTTTGGGGAGGG[C/T]GTGTTGGGATCAGCA	1108
rs746616224	snp	A/G	1.6477e-05	0.00287024	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581241	ACTAAAAGGAAGACT[A/G]GACTTACACATTTGT	1108
rs746625619	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6586091	GGCAACAGAGCAAGA[C/T]TCCGTATCAAAAAAA	1108
rs746658652	snp	A/C/T	3.31209e-05	0.00406935	intron-variant	CHD4	GRCh38.p7	12:6598186	CACTATCCTCTTCAT[A/C/T]GTAGCCCCTACATCT	1108
rs746659298	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6598592	GAGGCGGGCAGATCA[C/T]GAGGTCAAGAGATCG	1108
rs746685075	snp	C/T	1.77395e-05	0.00297816	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583051	GTTCATCAAAGTCTT[C/T]ATCACCTTCCTCTGA	1108
rs746694342	snp	A/G	1.70385e-05	0.00291873	missense	CHD4	GRCh38.p7	12:6601021	CATCAGGTACACGAG[A/G]GCTGCCCTTGGGCTT	1108
rs746712657	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6587110	TTTCATTTGTAAGGT[C/T]TAATAAAACACATAG	1108
rs746715532	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6597715	AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC	1108
rs746720098	snp	A/G	3.29457e-05	0.00405854	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581157	TCCTCTGAGGCAGGG[A/G]CAGGGGCCTGTGTAC	1108
rs746790932	snp	C/G	1.68752e-05	0.00290471	intron-variant	CHD4	GRCh38.p7	12:6593633	TTTGAGAAAAAAGAG[C/G]AGAGTCAGGACTGAG	1108
rs746810026	snp	C/T	1.64741e-05	0.00286998	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581335	TAACCTCCTTTTCTC[C/T]TTCTATGCTCTCTTC	1108
rs746824737	snp	A/G			missense	CHD4	GRCh38.p7	12:6602428	TCCCGAGGTTTCTTA[A/G]GCTTTTTCTTCTTCT	1108
rs746888835	in-del	-/AA			intron-variant	CHD4	GRCh38.p7	12:6575449	GTAAGACTTTGTCTC[-/AA]AAAAAAAAAAAAAAA	1108
rs746892584	snp	A/T	1.9509e-05	0.00312316	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606414	TGGCCCAGCTGCTCC[A/T]GCCGGCGGCCTGAGG	1108
rs746895158	snp	C/T	4.94597e-05	0.00497266	synonymous-codon	CHD4	GRCh38.p7	12:6591488	GCGGTCAATGGCCTC[C/T]TGCCGCATGTTCCCA	1108
rs746971757	snp	A/G	5.00638e-05	0.00500294	intron-variant	CHD4	GRCh38.p7	12:6600201	TTCCAAGGGGCCACA[A/G]TGGCCAGACACTCAC	1108
rs746978329	in-del	-/CCA			intron-variant	CHD4	GRCh38.p7	12:6605928	CCTCAACGCCCCCCT[-/CCA]CCACCACCACCACAA	1108
rs746979919	in-del	-/AA			intron-variant	CHD4	GRCh38.p7	12:6573916	TAACTGCAGCTACTC[-/AA]AAGAGGTTGAGGCAG	1108
rs746984687	snp	A/C	1.6691e-05	0.00288881	intron-variant	CHD4	GRCh38.p7	12:6588439	TAATAAAAGAACCAA[A/C]AACACCATTAGAAGT	1108
rs746989600	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6579096	GCAGCAGGCAGATCA[C/T]TTGAGGTCAGGAGTT	1108
rs747010374	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	CHD4	GRCh38.p7	12:6577812	AGCTAGAAATTTATT[C/T]TTGATCTCTAAGAAA	1108
rs747040203	in-del	-/G			intron-variant	CHD4	GRCh38.p7	12:6574944	TTTACATTTTAAAAT[-/G]GTTGGCAAAAAGTCA	1108
rs747080093	snp	C/T	0.000200666	0.0100146	intron-variant	CHD4	GRCh38.p7	12:6600514	TCATCCCATCACAAA[C/T]ATACAGAAGAGAAAC	1108
rs747081822	snp	A/G	1.65195e-05	0.00287393	intron-variant	CHD4	GRCh38.p7	12:6596140	CTTCTTGTCCACACT[A/G]CAAGTCCAGGAGAGA	1108
rs747127748	in-del	-/ATC	0.00036623	0.013527	cds-indel	CHD4	GRCh38.p7	12:6601966	TCCAGGCACCTTTGA[-/ATC]ATCATCATCATCCTC	1108
rs747157116	snp	A/G	1.64795e-05	0.00287045	synonymous-codon	CHD4	GRCh38.p7	12:6592731	AAAGTTGAGCAGATG[A/G]AACAACTCTTCCAGA	1108
rs747202436	snp	A/G	1.64806e-05	0.00287054	missense	CHD4	GRCh38.p7	12:6570895	TAGGTTCGGGTGCCC[A/G]GTTTGCCAGGCGGCT	1108
rs747281037	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6602840	GAGAACTAGATTTAG[A/G]CCTCCTGTAACTGGC	1108
rs747302320	snp	A/G	1.81747e-05	0.00301447	intron-variant	CHD4	GRCh38.p7	12:6598471	ATCATAACCATGGGA[A/G]GAGAAGGGACAGCCC	1108
rs747303727	snp	A/G	1.64974e-05	0.00287201	synonymous-codon	CHD4	GRCh38.p7	12:6592518	CAGTTTTTTTATCTG[A/G]TCCTCCTTGGCAATG	1108
rs747304242	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6596729	TGCTTGAACCCGGGC[A/G]GCGGAGGTTGCAGCA	1108
rs747311928	snp	G/T	1.65089e-05	0.00287301	missense	CHD4	GRCh38.p7	12:6578908	TCCACCTTCTCTACA[G/T]CAGCAGCACCTAGGG	1108
rs747314906	in-del	-/A	1.64917e-05	0.00287151	intron-variant	CHD4	GRCh38.p7	12:6577938	GGAAAAGTGCTCAGG[-/A]AAAACAAAACAAGGA	1108
rs747340253	snp	C/G	1.6483e-05	0.00287076	missense	CHD4	GRCh38.p7	12:6601376	CTGTCACCATGCTCT[C/G]CACCACAGCTACCGC	1108
rs747398729	snp	A/G	6.71817e-05	0.00579537	intron-variant	CHD4	GRCh38.p7	12:6571052	ATAGGGAGAAAAAGA[A/G]GTGGTGAGCTGTGGT	1108
rs747459716	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6595148	TTTCTGATGACAAAA[A/G]AAGAAAGTAATCCTA	1108
rs747483792	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6577954	AAAACAAAACAAGGA[A/G]AGTAAGAACCTCAAA	1108
rs747562292	snp	A/G/T			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583481	TCCTTTTCATGACTG[A/G/T]ACTCTTAAATACTTG	1108
rs747569270	snp	C/T	1.65111e-05	0.0028732	intron-variant	CHD4	GRCh38.p7	12:6599752	TCCCATTTTTTGCCC[C/T]GGCTGAGATCAGTCA	1108
rs747577530	snp	C/T	1.64798e-05	0.00287047	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581544	CTGAGAGGGAATTGC[C/T]GTGTGTCCTGCCAGA	1108
rs747628555	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6594259	GCCCTCAAATCTTCC[A/G]CTGTGTACATGTGTT	1108
rs747687310	in-del	-/A/C/CC			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608044	ATAGTCAGAAACTCA[-/A/C/CC]CCCCCCCCCATACTA	1108
rs747692303	snp	A/C	1.67992e-05	0.00289816	intron-variant	CHD4	GRCh38.p7	12:6588457	CACCATTAGAAGTGT[A/C]TCCTAAATTCCAATT	1108
rs747719184	snp	C/G	1.72288e-05	0.00293498	missense	CHD4	GRCh38.p7	12:6601038	CTGCCCTTGGGCTTC[C/G]TCCGAGCATTGGGAC	1108
rs747720649	in-del	-/C	1.65839e-05	0.00287953	frameshift-variant	CHD4	GRCh38.p7	12:6592034	CTTCAAAATTTCGAG[-/C]TGAGGATGTACTTGT	1108
rs747768498	snp	C/G	3.29511e-05	0.00405887	missense	CHD4	GRCh38.p7	12:6577836	TAAGAAATTGCCACG[C/G]TTCATTTCACCCTTG	1108
rs747774721	snp	A/C/G	3.32376e-05	0.00407651	synonymous-codon, missense	CHD4	GRCh38.p7	12:6594479	TGTAAAGGGAATACA[A/C/G]GAAGACTGCTGTCTG	1108
rs747780304	snp	C/G	3.39104e-05	0.00411753	intron-variant	CHD4	GRCh38.p7	12:6593639	AAAAAAGAGGAGAGT[C/G]AGGACTGAGGGCCCC	1108
rs747812828	snp	C/T	3.29571e-05	0.00405924	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581397	CCATCTTCTGCAGAA[C/T]AATAAAAGACAATCA	1108
rs747858696	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6605497	ACCCCAAAACACAGA[G/T]AGCGTAACCCCTAGC	1108
rs747889506	in-del	-/CC	1.6476e-05	0.00287014	intron-variant	CHD4	GRCh38.p7	12:6594423	TTCAAACACAAAACA[-/CC]CACACAAAAAACTAT	1108
rs747906347	snp	A/G	1.70994e-05	0.00292394	missense	CHD4	GRCh38.p7	12:6602063	TTCTTCTTCTTGCCA[A/G]GAGTATAGTCGCTGC	1108
rs747915525	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6599626	TTTCCCAGGACAAAA[A/G]TATCCCAACACTATA	1108
rs747942893	snp	A/G	1.65116e-05	0.00287324	intron-variant	CHD4	GRCh38.p7	12:6600398	ACCTCCTCCTCGCCT[A/G]GGCAAGGAAGAGGGA	1108
rs747965402	snp	A/G	1.64779e-05	0.00287031	synonymous-codon	CHD4	GRCh38.p7	12:6591533	GATGCGTTCGTATTT[A/G]TAACCTTCATGTTCC	1108
rs747971011	snp	G/T			synonymous-codon	CHD4	GRCh38.p7	12:6588384	CAAGGCCCCCAGCTC[G/T]AGTGGAAAGCAAGAA	1108
rs747980821	snp	A/G	3.29804e-05	0.00406068	intron-variant	CHD4	GRCh38.p7	12:6597870	CCACGGAGACTGCCC[A/G]TCTCCCGTGTGCTCA	1108
rs747981285	in-del	-/GA			intron-variant	CHD4	GRCh38.p7	12:6576631	TGTCTTTTTTGAGGT[-/GA]GTCTCGCTCTGTCGC	1108
rs747990661	in-del	-/AA			intron-variant	CHD4	GRCh38.p7	12:6572876	GGAGTCCATCTCTTT[-/AA]AAAAAAAAAAAGGCA	1108
rs748033659	snp	A/G	1.65518e-05	0.00287674	intron-variant	CHD4	GRCh38.p7	12:6578924	CAGCAGCACCTAGGG[A/G]AAGAAATGTTATTGA	1108
rs748176738	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6579369	ATGGGTGGATCTCTT[C/G]AGGTCAGGAGTTCAT	1108
rs748237657	snp	C/G	1.70061e-05	0.00291595	missense	CHD4	GRCh38.p7	12:6606302	GGGCAGGCTGTTGTT[C/G]AAAAGTGCATCCATA	1108
rs748238713	snp	A/G	1.64773e-05	0.00287026	synonymous-codon	CHD4	GRCh38.p7	12:6592745	GAAACAACTCTTCCA[A/G]ATTGTTTTGTAATGG	1108
rs748239977	snp	G/T	4.95094e-05	0.00497517	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581031	CAAACAAAAAAAATG[G/T]GGATACCTTTACCTT	1108
rs748311291	snp	C/G	1.64841e-05	0.00287085	intron-variant	CHD4	GRCh38.p7	12:6599764	CCCCGGCTGAGATCA[C/G]TCACTCACCGTACAA	1108
rs748328749	snp	A/G	1.64958e-05	0.00287187	intron-variant	CHD4	GRCh38.p7	12:6587669	CCCTAACCTTTAGAG[A/G]GGCCAAGCCCCACAC	1108
rs748350791	snp	A/G/T	3.40143e-05	0.00412386	missense	CHD4	GRCh38.p7	12:6606348	CCCGCCGAGCAGGGG[A/G/T]ACGGGGAGCCCAGGC	1108
rs748388806	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6590799	ACTGCTCTCCAGCCT[C/T]GGCAACAGAGTGAGA	1108
rs748416883	snp	A/G	3.29592e-05	0.00405938	intron-variant	CHD4	GRCh38.p7	12:6587562	TTGTTGTCTCCTCCT[A/G]TAAAAAATCAAGGGC	1108
rs748435011	snp	A/C	1.64972e-05	0.00287199	missense	CHD4	GRCh38.p7	12:6593120	TCTTCAGCCGATGGG[A/C]TTCATCCACGATGAG	1108
rs748453042	snp	A/G	1.65392e-05	0.00287564	intron-variant	CHD4	GRCh38.p7	12:6595288	GACTGCAGCAAAGAT[A/G]CATTGTCCTACCCAA	1108
rs748466140	snp	A/G	1.6939e-05	0.00291019	intron-variant	CHD4	GRCh38.p7	12:6571066	AGGTGGTGAGCTGTG[A/G]TGGCCCAGACTGAGC	1108
rs748476720	in-del	-/T	1.64783e-05	0.00287034	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581565	CCTGCCAGACTACCC[-/T]TGTTAGAACTGAGCA	1108
rs748495140	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6571304	TTATTCGTTTTTTCT[A/C]TTCTCTACCTTCAGA	1108
rs748505910	snp	A/G	1.64727e-05	0.00286986	missense	CHD4	GRCh38.p7	12:6599934	CATCCTCCTCTTCGA[A/G]GTCTCCCCCAACCTC	1108
rs748591406	snp	A/C	3.31444e-05	0.00407076	intron-variant	CHD4	GRCh38.p7	12:6595466	ACAGCTGCCCAAAAT[A/C]CTTTTCTATAGAAGA	1108
rs748658269	snp	A/G	1.65203e-05	0.002874	missense	CHD4	GRCh38.p7	12:6578480	TGTTTCTCATCATTC[A/G]GGTCCTTGGGGGTCT	1108
rs748659505	in-del	-/A			intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581021	AACAAACAAACAAAC[-/A]AAAAAAATGTGGATA	1108
rs748666271	snp	A/G	1.65677e-05	0.00287812	intron-variant	CHD4	GRCh38.p7	12:6602197	CAGGGCAAGGGGGGA[A/G]GAGGGAGACAGACAC	1108
rs748669964	snp	C/T			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569770	AGGTGTTAAAACCGT[C/T]CCATGTACTTCACTG	1108
rs748716140	in-del	-/AG	6.70252e-05	0.00578862	intron-variant	CHD4	GRCh38.p7	12:6571049	TGCATAGGGAGAAAA[-/AG]AGGTGGTGAGCTGTG	1108
rs748735931	snp	C/T	1.64732e-05	0.0028699	missense	CHD4	GRCh38.p7	12:6595392	TTCACCTTCTTGAGC[C/T]TCTTGCCTGGTCGGC	1108
rs748763637	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6584967	GCCACACTTACATAT[A/C]AACTGAGGTTGGACG	1108
rs748803108	snp	C/T	0.000132103	0.00812612	synonymous-codon	CHD4	GRCh38.p7	12:6594495	GAAGACTGCTGTCTG[C/T]ACAGTTTTCCCAAGG	1108
rs748916163	snp	C/G	0.00028434	0.0119201	intron-variant	CHD4	GRCh38.p7	12:6600440	TTGGAAAAAAACTAC[C/G]TCCCCCCACCCCCCG	1108
rs748943517	snp	C/G	1.64806e-05	0.00287054	missense	CHD4	GRCh38.p7	12:6591566	GAAATCCTCTAGCAG[C/G]TCTAGCATCTTGGTC	1108
rs748999342	snp	A/G	3.42284e-05	0.00413679	intron-variant	CHD4	GRCh38.p7	12:6594681	GAGAAGTCAAGAGCT[A/G]GCAAGGAACTCCCCT	1108
rs749032050	in-del	-/AGAGAAGTCA	1.68755e-05	0.00290473	intron-variant	CHD4	GRCh38.p7	12:6594665	GCTGAAGGATGAAAC[-/AGAGAAGTCA]AGAGCTGGCAAGGAA	1108
rs749055521	snp	A/G	1.65258e-05	0.00287448	synonymous-codon	CHD4	GRCh38.p7	12:6600625	ATAGCTATTGATACT[A/G]GCATCATCGAAGTCA	1108
rs749106775	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6575913	ACATCTTTGCCCAAC[C/T]TAATCCCTTTGTTCA	1108
rs749107637	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6579676	GAATCACTTGAACCC[A/C]GGAGGCGGAGGTTGC	1108
rs749114351	snp	A/G	0.000297093	0.0121844	synonymous-codon	CHD4	GRCh38.p7	12:6593136	TTCATCCACGATGAG[A/G]CAGGCCCAATCAATA	1108
rs749125214	in-del	-/C	1.65392e-05	0.00287564	intron-variant	CHD4	GRCh38.p7	12:6598179	TTTTGTCACTATCCT[-/C]CTTCATCGTAGCCCC	1108
rs749140179	snp	A/G	3.32806e-05	0.00407912	intron-variant	CHD4	GRCh38.p7	12:6600530	ATACAGAAGAGAAAC[A/G]CACCTTTCTTTTTCT	1108
rs749142192	snp	C/G	3.3189e-05	0.0040735	missense, intron-variant	CHD4	GRCh38.p7	12:6602175	GGCATAAGAGCATAC[C/G]CTGGAGCAGGGCAAG	1108
rs749193541	snp	A/C/G	4.94184e-05	0.00497063	synonymous-codon, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581132	AGGGGGTTCAACAAC[A/C/G]ACCTTTTCATCCTCT	1108
rs749205441	snp	G/T	1.6507e-05	0.00287284	missense	CHD4	GRCh38.p7	12:6598011	TTTCGGCTTTTCTCT[G/T]CATCACCACCAAAGT	1108
rs749251148	snp	C/T	1.70009e-05	0.0029155	missense	CHD4	GRCh38.p7	12:6606313	TGTTCAAAAGTGCAT[C/T]CATATCCTCCTCCTC	1108
rs749279386	snp	C/T	1.64811e-05	0.00287059	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581044	TGTGGATACCTTTAC[C/T]TTTGGGCTCTGTCTC	1108
rs749279937	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6588596	CAGCCTGGCCAACAC[A/G]GTGAAACCCTGTCTC	1108
rs749352272	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6593803	ACCCAAGGTCCCACC[A/G]TAACTACAAGTCTTA	1108
rs749365432	snp	A/G	1.64789e-05	0.0028704	intron-variant	CHD4	GRCh38.p7	12:6601610	AAGAGAGAACAGAAA[A/G]ATTCTCCTCCCCCTT	1108
rs749373617	snp	G/T	1.64974e-05	0.00287201	synonymous-codon	CHD4	GRCh38.p7	12:6593428	TACCTTCATGCGGGA[G/T]GCCTTCTTGCCACCA	1108
rs749395335	snp	A/T	1.64751e-05	0.00287007	missense	CHD4	GRCh38.p7	12:6573118	TTTCCTGCCATTGAC[A/T]CCTTGGACAGGTGCT	1108
rs749408168	in-del	-/AAAGAGGT	3.34851e-05	0.00409163	intron-variant	CHD4	GRCh38.p7	12:6571046	ACTGCATAGGGAGAA[-/AAAGAGGT]AAAGAGGTGGTGAGC	1108
rs749412921	snp	C/G	1.70731e-05	0.00292169	intron-variant	CHD4	GRCh38.p7	12:6600064	CACCCGCCCACCGCA[C/G]TCTGAAGCCAGTGCC	1108
rs749506496	snp	A/C	9.88712e-05	0.00703035	missense	CHD4	GRCh38.p7	12:6601764	AGCAGATGATTTAGG[A/C]TCCTGCAGAAAGAGC	1108
rs749512768	snp	A/C			missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581379	TTTTCCTCTATTTTT[A/C]TCCCATCTTCTGCAG	1108
rs749557139	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	CHD4	GRCh38.p7	12:6599971	GATCTCCTCACCCTC[C/T]GAATTGTCCTCTTTA	1108
rs749570554	snp	C/T	1.65833e-05	0.00287948	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581644	GATAGGACAGGCAGA[C/T]TTACCAGCAGGTGGG	1108
rs749592811	snp	G/T	1.6473e-05	0.00286988	missense	CHD4	GRCh38.p7	12:6602386	CTCACCTCCTTTTTT[G/T]GGCGCTTGCTCTTAG	1108
rs749593256	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6605201	GCAGAAGTGAATGAT[A/G]CTGGATGAGAAACAA	1108
rs749598035	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6592166	TCCCACTTTGGAACT[A/C]AGGACACCTAACGCA	1108
rs749625632	snp	A/G	1.65296e-05	0.00287481	synonymous-codon	CHD4	GRCh38.p7	12:6578491	ATTCAGGTCCTTGGG[A/G]GTCTCTCCATTCTGA	1108
rs749651125	in-del	-/CA			intron-variant	CHD4	GRCh38.p7	12:6577417	ACAGAGATTCTGCCT[-/CA]AAAAAAAAAAAAAAA	1108
rs749652793	snp	A/G	4.9953e-05	0.0049974	intron-variant	CHD4	GRCh38.p7	12:6595476	AAAATCCTTTTCTAT[A/G]GAAGAAACAACTTGG	1108
rs749752548	snp	A/C	3.50116e-05	0.00418384	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583109	GGACTGGTCGTCCTG[A/C]CAATCTGGAGGGAGA	1108
rs749805831	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	CHD4	GRCh38.p7	12:6602460	GAGCTTTGGAGTCTC[C/T]GTTTCTGACAAATCC	1108
rs749831340	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6604207	TTGAGCCCGGGAGGC[A/G]GAGGTTGCAGTGAGC	1108
rs749844243	in-del	-/CTT	3.33314e-05	0.00408223	intron-variant	CHD4	GRCh38.p7	12:6591454	GAAACTAAACAACTC[-/CTT]CTCTCTCACCATTGA	1108
rs749846082	snp	A/C	1.6643e-05	0.00288465	intron-variant	CHD4	GRCh38.p7	12:6592067	TATTTCCTACATGGG[A/C]AAGGTAGAAAGACAG	1108
rs749856778	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6572572	CCCATCTCTTTTTTT[C/T]CTGGAGTCTCACTAT	1108
rs749874127	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6571694	GCTGGGGCGCAGTGG[C/G]TCATGCCTATAATCC	1108
rs749874899	snp	A/G	9.68476e-05	0.00695805	intron-variant	CHD4	GRCh38.p7	12:6578710	CCCACTGACAACTAA[A/G]TGTGGGGACAGGTAC	1108
rs749935735	snp	C/T	0.000117916	0.00767749	intron-variant	CHD4	GRCh38.p7	12:6600045	AGATTCAGATTATTA[C/T]CCCCACCCGCCCACC	1108
rs749944834	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6586835	CCCGAACACCTGGGA[C/T]TACAGGTGTGCTTCA	1108
rs749946654	snp	G/T	0.00304098	0.0388747	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581704	CCCTGGAGTGGAGGG[G/T]GTAGGAGTTTTTGGG	1108
rs749962700	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6599401	GCTATGACTGCACCA[C/T]TGCACTCTAGCCCGG	1108
rs749989939	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	CHD4	GRCh38.p7	12:6602439	CTTAGGCTTTTTCTT[C/T]TTCTTGAGCTTTGGA	1108
rs749992297	snp	G/T	1.66217e-05	0.0028828	intron-variant	CHD4	GRCh38.p7	12:6595988	AAACAACTCTATGCC[G/T]CACCCAAAATCACTC	1108
rs750043969	snp	A/G	1.65433e-05	0.002876	stop-gained	CHD4	GRCh38.p7	12:6592008	GGTTGCCACCACCTC[A/G]GGCATTGAGTGCTTC	1108
rs750054935	snp	C/T	0.000183587	0.00957914	intron-variant	CHD4	GRCh38.p7	12:6578675	GGGTGTCTCTCAGAC[C/T]CAGAAAATGGTGCCA	1108
rs750104158	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6580581	GCATGGTGGTACATG[C/T]CTGTAATCCCAGCTA	1108
rs750126199	snp	A/G	1.65353e-05	0.00287531	intron-variant	CHD4	GRCh38.p7	12:6595457	AGACATCACACAGCT[A/G]CCCAAAATCCTTTTC	1108
rs750139114	snp	A/G	1.80948e-05	0.00300784	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581835	GCAATGGGACAAGAA[A/G]TTGAAGACCCAATTC	1108
rs750157676	snp	G/T	1.65149e-05	0.00287353	intron-variant	CHD4	GRCh38.p7	12:6570848	CAGGAAGAGGTGGTG[G/T]CAAGAAGAAAATGGT	1108
rs750175656	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6595910	TTGCAGTGAGTCAAG[A/G]TCACGCCACTGCACT	1108
rs750177796	snp	C/G	1.68792e-05	0.00290505	missense	CHD4	GRCh38.p7	12:6601005	GGTTTAGGCTTCTTG[C/G]CATCAGGTACACGAG	1108
rs750214515	snp	A/C/G	0.000131892	0.00811974	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570665	GGTGGAGGTGGTATC[A/C/G]GTCTGCATCTTCACT	1108
rs750234213	snp	C/T			missense	CHD4	GRCh38.p7	12:6578917	TCTACATCAGCAGCA[C/T]CTAGGGGAAGAAATG	1108
rs750244207	snp	A/T	1.76796e-05	0.00297312	intron-variant	CHD4	GRCh38.p7	12:6592370	TGTCTAAATGGAGTC[A/T]GCTTCTGTCCCTCCC	1108
rs750260250	snp	A/C	1.73252e-05	0.00294318	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583010	TAGAAAAGCAACAAA[A/C]AAAGCACAGCCCTCA	1108
rs750264299	in-del	-/AAAT			intron-variant	CHD4	GRCh38.p7	12:6586405	ATTCCATCTCAAAAT[-/AAAT]AAATAAATAAATACA	1108
rs750321093	snp	C/T	1.66468e-05	0.00288498	missense	CHD4	GRCh38.p7	12:6598377	GAGATGGTGGCTGAC[C/T]CCACTTCCAGATTAG	1108
rs750355009	snp	G/T	1.64741e-05	0.00286998	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581310	ATGGCAGTCTCAGGG[G/T]CTGTAGATTTAACCT	1108
rs750400791	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6603735	CTAAGAGAAGAACTC[C/G]ATCACTCCCTCAATC	1108
rs750402336	snp	A/G	1.64776e-05	0.00287028	missense	CHD4	GRCh38.p7	12:6577877	TGAGGATGGCATAGC[A/G]TGGGTCATTCTGGAT	1108
rs750405242	snp	A/C	0.000132157	0.0081278	missense	CHD4	GRCh38.p7	12:6598281	GCCATTTCACAAAGA[A/C]CTGCCGCTCTGGCCG	1108
rs750422123	in-del	-/A	1.64798e-05	0.00287047	intron-variant	CHD4	GRCh38.p7	12:6587563	GTTGTCTCCTCCTAT[-/A]AAAAAATCAAGGGCC	1108
rs750489736	snp	A/T	0.000131904	0.00812002	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581463	TTTCTTCCCAGTTTG[A/T]CTCATCTTAAATTGT	1108
rs750497294	snp	A/G			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569652	GGCCTCCGGGGGTGT[A/G]GGATTGAGGCTGTGT	1108
rs750504212	snp	A/G			utr-variant-3-prime	CHD4	GRCh38.p7	12:6570433	AGAAGCCAGGGTCCA[A/G]AAGGCCAGCCCGCCA	1108
rs750511072	snp	A/C	1.75934e-05	0.00296587	intron-variant	CHD4	GRCh38.p7	12:6594423	TTCAAACACAAAACA[A/C]CCACACAAAAAACTA	1108
rs750511840	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6585348	GGAGTGCAGTGGGGC[A/G]ATCTTGGCTCACTGC	1108
rs750514164	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6576993	ACAGGCTGGAGTGCC[A/G]TAGCACGATCTCAGC	1108
rs750548651	in-del	-/AG	3.29636e-05	0.00405964	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581435	AGAAGGTACTAGATC[-/AG]AGAGAAGGTCATTTC	1108
rs750582102	snp	C/G	1.77738e-05	0.00298104	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582582	TAGCAGAAGCCCTTG[C/G]TCTAGATCAGTCCAC	1108
rs750603925	snp	C/T	3.34874e-05	0.00409177	intron-variant	CHD4	GRCh38.p7	12:6600505	ACTCCCACCTCATCC[C/T]ATCACAAATATACAG	1108
rs750632197	snp	G/T	1.64874e-05	0.00287113	intron-variant	CHD4	GRCh38.p7	12:6591617	TTAATTATGGAAGAG[G/T]CAGATGGTAATCCCT	1108
rs750691024	in-del	-/CC	1.78713e-05	0.00298921	intron-variant	CHD4	GRCh38.p7	12:6600898	TAGACATGGCACCCT[-/CC]CCCTAAAGCGATGGG	1108
rs750708586	snp	A/G	1.64762e-05	0.00287016	synonymous-codon	CHD4	GRCh38.p7	12:6594567	GGAGAAGCGCAACCA[A/G]TTCAGGCCCTCCATT	1108
rs750713669	snp	A/G			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608325	AATCTCTTTTCCTCT[A/G]ACACTGGAAAGCTAT	1108
rs750723824	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6576530	ATGTTGCCCGAGCTA[G/T]TCTTGAACTCCTGGA	1108
rs750784889	snp	C/T	1.65121e-05	0.00287329	intron-variant	CHD4	GRCh38.p7	12:6597856	TTAGCAGGACTCTCC[C/T]ACGGAGACTGCCCGT	1108
rs750800178	snp	A/G	3.31741e-05	0.00407259	synonymous-codon	CHD4	GRCh38.p7	12:6600571	TCGGAGTTTCTTGCG[A/G]CTGCGGCTACTACGG	1108
rs750825827	snp	A/G	1.65252e-05	0.00287443	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582692	CTGAGGTGGCATACC[A/G]TATCGCATAATTGCA	1108
rs750832779	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6596575	GAGGCCAAGGCAGGC[A/G]GATCACCTGAGGTCG	1108
rs750876187	snp	A/G	1.70452e-05	0.0029193	synonymous-codon	CHD4	GRCh38.p7	12:6606332	ATCCTCCTCCTCACT[A/G]CCCGCCGAGCAGGGG	1108
rs750954893	snp	A/G	1.64936e-05	0.00287168	missense	CHD4	GRCh38.p7	12:6571008	GCTTTCATGTCACTC[A/G]GCAGTTCTTCCAGCT	1108
rs750978209	snp	A/C/G	8.24499e-05	0.00642023	synonymous-codon	CHD4	GRCh38.p7	12:6592707	TTACTGGAACCTCTC[A/C/G]GGGGTGAGAAAGTTG	1108
rs750984477	in-del	-/G	0.00122461	0.0247145	intron-variant	CHD4	GRCh38.p7	12:6595972	AAAAAAAAAAAAAAA[-/G]AAACAACTCTATGCC	1108
rs751049651	snp	A/G	4.86275e-05	0.00493066	intron-variant	CHD4	GRCh38.p7	12:6578694	AAAATGGTGCCATTG[A/G]CCCACTGACAACTAA	1108
rs751060480	snp	C/G/T	6.60115e-05	0.00574476	missense	CHD4	GRCh38.p7	12:6596029	CCAATAGCTCTGCTT[C/G/T]AACAGGTCGTAATCC	1108
rs751085723	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6589258	TGTAATCAAGGTCCA[A/C]TGACGAATACTAATA	1108
rs751181610	snp	A/G	0.000132061	0.00812485	intron-variant, upstream-variant-2KB, missense	CHD4, SCARNA11	GRCh38.p7	12:6583186	GTGGGGGGCGGGGCC[A/G]GCCACACACACCTCG	1108
rs751212891	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6599601	CCTCAGTTTGAAGTT[A/G]GTCCTATATTTTCCC	1108
rs751256918	snp	A/G	3.31576e-05	0.00407157	intron-variant	CHD4	GRCh38.p7	12:6596170	AAAACCCTCAGAGCC[A/G]GAAAAGGCAACCCTC	1108
rs751257937	in-del	-/AAAG			intron-variant	CHD4	GRCh38.p7	12:6602667	AGGACAAAAACAGAC[-/AAAG]AGAGAGCTGTATATA	1108
rs751280685	snp	C/G	1.65127e-05	0.00287334	intron-variant	CHD4	GRCh38.p7	12:6602544	GGAAAAGATCAATAG[C/G]AAAAGGTTAGGCCCT	1108
rs751323344	snp	A/C	1.66932e-05	0.002889	intron-variant	CHD4	GRCh38.p7	12:6587351	TTTTCAGACCAATTA[A/C]CAAGCACAGGATTGC	1108
rs751336784	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6580884	TGATGGCGTCTGTCT[A/G]TAATCCCAGCTCCTC	1108
rs751395634	snp	G/T	1.64811e-05	0.00287059	missense	CHD4	GRCh38.p7	12:6601334	TAGGCACCTCCACAG[G/T]GGGAGGTGGTGGTGC	1108
rs751432025	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6592569	ACCTTCCAAATTGCT[C/T]CAGAAAGAAAAAGGA	1108
rs751476341	snp	C/G	1.64795e-05	0.00287045	synonymous-codon	CHD4	GRCh38.p7	12:6594597	TTGATAGGGGTGCAG[C/G]GTTCCACCTGTAGCA	1108
rs751516106	snp	C/T	3.29571e-05	0.00405924	synonymous-codon	CHD4	GRCh38.p7	12:6577896	GTCATTCTGGATGTC[C/T]TGCCACCGGGCATAG	1108
rs751520080	snp	C/G	1.64781e-05	0.00287033	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581588	ACTGAGCACAGGGGA[C/G]CAGAAAAATAGGCCA	1108
rs751534948	snp	A/G	1.70226e-05	0.00291736	splice-donor-variant	CHD4	GRCh38.p7	12:6594457	ACCCCAGATTTCCTT[A/G]CCTCCTTGTAAAGGG	1108
rs751565482	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6593731	CTGACACACCTGCGC[A/T]GCTGCTCCTGCTCTC	1108
rs751585626	snp	C/T	6.64849e-05	0.00576524	missense, intron-variant	CHD4	GRCh38.p7	12:6602159	CTGTCCCCCAGCTGC[C/T]GGCATAAGAGCATAC	1108
rs751600831	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6603943	CCAACATATGGGAAT[C/G]TCTGCACAAAAAAAC	1108
rs751605937	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6604833	CTCCTGCGCAGCTCC[C/T]GGTCAACATGAAAGG	1108
rs751612749	snp	C/T	6.59805e-05	0.00574333	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581484	CTTAAATTGTCCTCT[C/T]GTGCCTTTAAGAGCC	1108
rs751667316	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6600892	TTTCTATTAGACATG[A/G]CACCCTCCCTAAAGC	1108
rs751683940	in-del	-/GT	1.64735e-05	0.00286993	frameshift-variant	CHD4	GRCh38.p7	12:6587859	CTTCTTTGCCACCTG[-/GT]CGTGATGCGCTCCTC	1108
rs751697831	snp	A/C	1.73327e-05	0.00294381	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581016	CTCAAAACAAACAAA[A/C]AAACAAAAAAAATGT	1108
rs751716825	snp	A/G	1.65529e-05	0.00287683	synonymous-codon	CHD4	GRCh38.p7	12:6578052	GCCGGCTAGCAGCCA[A/G]TAGTCATGCCGTCGA	1108
rs751746075	snp	A/C	1.66228e-05	0.0028829	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582823	ATCTGACACTCACCC[A/C]TCCTTAGAATCGTAT	1108
rs751788491	snp	C/T	1.64825e-05	0.00287071	missense	CHD4	GRCh38.p7	12:6597954	CCATAGCGATAGAAG[C/T]GTTCCTCCATCTCTG	1108
rs751790459	snp	A/C	1.66496e-05	0.00288522	intron-variant	CHD4	GRCh38.p7	12:6600707	GGTTAGACGTTCAAG[A/C]CAAGGGGAAGGACAG	1108
rs751867169	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6586428	TAAATACATACATAC[A/G]TACATACACAAGGAG	1108
rs751874379	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6585561	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGTC	1108
rs751875901	in-del	-/TTT	1.64953e-05	0.00287182	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581490	TTGTCCTCTCGTGCC[-/TTT]AAGAGCCAGCCCTAT	1108
rs751877653	snp	A/G	3.31208e-05	0.00406931	missense	CHD4	GRCh38.p7	12:6600585	GGCTGCGGCTACTAC[A/G]GCTGGTGGAACCATC	1108
rs751883549	snp	G/T	1.64893e-05	0.0028713	synonymous-codon	CHD4	GRCh38.p7	12:6573084	GCTACCTTTGTGCAG[G/T]ACTGCATTGGCTGGC	1108
rs751890132	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6571116	CAGCCCCCCATCACT[G/T]CTCAGTGACCAAGTA	1108
rs751893060	snp	A/C	1.70214e-05	0.00291726	missense	CHD4	GRCh38.p7	12:6606337	CCTCCTCACTGCCCG[A/C]CGAGCAGGGGGACGG	1108
rs751939837	snp	C/G/T	3.29453e-05	0.00405854	missense, synonymous-codon	CHD4	GRCh38.p7	12:6599929	GTGGTCATCCTCCTC[C/G/T]TCGAGGTCTCCCCCA	1108
rs751960931	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6598153	TGTTCATTCCTTCTA[C/T]CCACAAGGCTCTTTT	1108
rs751963093	snp	A/C	1.6534e-05	0.00287519	intron-variant	CHD4	GRCh38.p7	12:6593077	GGCTCCAACATCCCT[A/C]CCTCAGCCCTCACCT	1108
rs751995115	snp	A/G	6.58913e-05	0.00573945	synonymous-codon	CHD4	GRCh38.p7	12:6601710	CTCCTCTGAGAACAC[A/G]TGGTCAATGTCTTCC	1108
rs752049117	snp	A/G			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608494	ACCCCTATACCCTTC[A/G]AGCCAGGCATCCCAT	1108
rs752074782	in-del	-/A			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581858	CCCAATTCCAGCTAC[-/A]GGCTCCTTTCCTATT	1108
rs752078735	in-del	-/A	1.65971e-05	0.00288067	intron-variant	CHD4	GRCh38.p7	12:6595994	CTCTATGCCTCACCC[-/A]AAATCACTCACCTGT	1108
rs752079760	snp	A/G	4.95111e-05	0.00497525	intron-variant	CHD4	GRCh38.p7	12:6601558	TGCACAAGAGCAGAG[A/G]GAAAGGTTTAAGAAT	1108
rs752127850	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6575629	CCCTTAACACCTCAT[C/G]ATTATATGACAGTTT	1108
rs752143656	in-del	-/CTT	0.0217	0.101878	cds-indel	CHD4	GRCh38.p7	12:6602040	TTTCTTAGGTCCAAG[-/CTT]CTTCTTCTTCTTCTT	1108
rs752148706	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6596629	GCATGGAGAAACCCC[A/G]TCTCTACTAAAAATG	1108
rs752197619	snp	A/G	1.64743e-05	0.00287	synonymous-codon	CHD4	GRCh38.p7	12:6570977	GGCAATGGTAGCTGG[A/G]AGTCGAGTCACATCA	1108
rs752218285	snp	A/G	5.11653e-05	0.00505767	missense	CHD4	GRCh38.p7	12:6606285	TTACCTGGGTGGGGT[A/G]GGGGCAGGCTGTTGT	1108
rs752225434	snp	A/C	0.000100174	0.00707649	intron-variant	CHD4	GRCh38.p7	12:6601253	CATCTTAAGCCCACA[A/C]TAGACACCCCCACTC	1108
rs752260626	snp	A/T	3.30038e-05	0.00406212	intron-variant	CHD4	GRCh38.p7	12:6587600	CCCAAAGTCAGTTTC[A/T]GCAGCTGCAGTGGAA	1108
rs752286672	snp	A/G	1.66463e-05	0.00288494	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6580994	CCTGGCGGCAGCACT[A/G]CACTGTCTCAAAACA	1108
rs752302054	in-del	-/AAAG	1.64953e-05	0.00287182	intron-variant	CHD4	GRCh38.p7	12:6601578	GGTTTAAGAATAAAA[-/AAAG]AAAGAGAAGTAAGAA	1108
rs752326362	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6589449	TATGAACATCATGTC[C/T]GTCCCCCAGTATGAT	1108
rs752335499	snp	C/T	8.26904e-05	0.00642949	intron-variant	CHD4	GRCh38.p7	12:6599736	AGAAAAGACTACACT[C/T]TCCCATTTTTTGCCC	1108
rs752362997	snp	G/T	1.64953e-05	0.00287182	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581491	TGTCCTCTCGTGCCT[G/T]TAAGAGCCAGCCCTA	1108
rs752421605	snp	A/G	0.000115355	0.00759368	synonymous-codon	CHD4	GRCh38.p7	12:6601338	CACCTCCACAGGGGG[A/G]GGTGGTGGTGCAACC	1108
rs752422112	snp	C/T	1.65307e-05	0.0028749	synonymous-codon	CHD4	GRCh38.p7	12:6594621	TGTAGCATCCAGGTA[C/T]TCTGGCTGTCGCTCA	1108
rs752452916	snp	C/T	6.63647e-05	0.00576003	intron-variant	CHD4	GRCh38.p7	12:6587368	AAGCACAGGATTGCC[C/T]TGGATTCATACTCAC	1108
rs752458786	snp	C/T	4.94442e-05	0.00497188	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581597	AGGGGAGCAGAAAAA[C/T]AGGCCAGGACAAAAA	1108
rs752468440	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6589520	ACGCCTGTAATCCCA[C/G]CACTTTGGGAAGCTG	1108
rs752484356	in-del	-/G	1.65241e-05	0.00287433	intron-variant	CHD4	GRCh38.p7	12:6570835	CAGAATGGTTCTGCA[-/G]GAAGAGGTGGTGTCA	1108
rs752502512	in-del	-/ACAGGT	4.7619e-05	0.00487927	intron-variant	CHD4	GRCh38.p7	12:6578718	CAACTAAATGTGGGG[-/ACAGGT]ACAGTCTTTTATCTT	1108
rs752531665	snp	A/G	1.64727e-05	0.00286986	missense	CHD4	GRCh38.p7	12:6599858	TAGGAAGAAGGACAG[A/G]TATCACAGCAGAGCA	1108
rs752572057	snp	C/T			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6570020	TTTCAACTATACAGG[C/T]GCCAGGCTCCTGCCG	1108
rs752624787	snp	A/C	3.29451e-05	0.00405851	missense	CHD4	GRCh38.p7	12:6600596	CTACGGCTGGTGGAA[A/C]CATCAGAAACAGAAT	1108
rs752632870	snp	A/G	3.29533e-05	0.00405901	intron-variant	CHD4	GRCh38.p7	12:6591843	GAGAACAAATGCAAA[A/G]AAAAAAGTATTAAAA	1108
rs752672722	snp	A/T	1.67685e-05	0.00289551	intron-variant	CHD4	GRCh38.p7	12:6578366	AAGAACCCCAATTTC[A/T]CATCAGATCCTTCTA	1108
rs752696922	snp	A/G			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582392	ATGGCTCCACCTTGA[A/G]GTAAAGCCCACCACT	1108
rs752716138	snp	A/G	3.336e-05	0.00408398	intron-variant	CHD4	GRCh38.p7	12:6600718	CAAGCCAAGGGGAAG[A/G]ACAGAGTGGCAGAGA	1108
rs752720902	snp	A/C/T	3.29741e-05	0.00406031	intron-variant	CHD4	GRCh38.p7	12:6595327	AGTCCCTTCCACCCC[A/C/T]ACTCACATCAACTGT	1108
rs752724519	snp	A/G	1.64738e-05	0.00286995	intron-variant	CHD4	GRCh38.p7	12:6591905	GAGGAACAGGAGATG[A/G]CACTACATACCATTG	1108
rs752730611	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6594809	TTACTGCAATTTCAT[A/G]TTCAGTTTAGGGTCC	1108
rs752750067	snp	G/T	0.000148656	0.00862008	missense	CHD4	GRCh38.p7	12:6598337	GTGTTGGGATCAGCA[G/T]CTGGAGGCCGAGGCA	1108
rs752786970	snp	A/C/G	4.98752e-05	0.00499355	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582835	CCCCTCCTTAGAATC[A/C/G]TATGGCACTTACTTC	1108
rs752892972	snp	A/C			intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581186	ACACTTCAAAGGAAA[A/C]AAAAACAAAAACAAA	1108
rs752930501	snp	A/C	1.66147e-05	0.0028822	intron-variant	CHD4	GRCh38.p7	12:6593374	AAACTAAGCCAGAAG[A/C]CACAACTCTTTCTCT	1108
rs752949357	snp	C/T	1.65113e-05	0.00287322	intron-variant	CHD4	GRCh38.p7	12:6577734	TGCTGCAGGACGTTA[C/T]GCACTTTCAAGTTTG	1108
rs752982860	snp	C/G	1.64727e-05	0.00286986	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581118	TTCTCCTCTCCCTCA[C/G]GGGGTTCAACAACGA	1108
rs753004819	in-del	-/CT	0.000363618	0.0134788	intron-variant	CHD4	GRCh38.p7	12:6593407	GGTGGCTTCCCTCCC[-/CT]GAGATACCTTCATGC	1108
rs753025193	in-del	-/G	0.00011716	0.00765285	intron-variant	CHD4	GRCh38.p7	12:6588450	CCAAAAACACCATTA[-/G]AAGTGTCTCCTAAAT	1108
rs753074787	snp	G/T	1.64735e-05	0.00286993	synonymous-codon	CHD4	GRCh38.p7	12:6601743	GCCCCAGTCTTCCAG[G/T]AGCTGAGCAGATGAT	1108
rs753093130	snp	A/G	1.6865e-05	0.00290383	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581005	CACTACACTGTCTCA[A/G]AACAAACAAACAAAC	1108
rs753112949	snp	A/G	7.52177e-05	0.00613214	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582095	GGTGTGAGCCACTGC[A/G]CCTGGCCCCCTAGAA	1108
rs753114263	snp	C/T	1.64757e-05	0.00287012	synonymous-codon	CHD4	GRCh38.p7	12:6587881	GCGCTCCTCCACTGA[C/T]GCACGGGTCACAAAC	1108
rs753126817	snp	A/G	1.64822e-05	0.00287068	synonymous-codon	CHD4	GRCh38.p7	12:6593566	CTCCCGCTCCCAGTT[A/G]ATGATGGTAGAAAGA	1108
rs753138255	snp	A/G	1.64789e-05	0.0028704	synonymous-codon	CHD4	GRCh38.p7	12:6600262	AGCCTTCTCCATGTC[A/G]GGATCCAGGCAGACC	1108
rs753139884	snp	C/T	1.67458e-05	0.00289355	synonymous-codon	CHD4	GRCh38.p7	12:6573258	CTCAATCACCAGAGC[C/T]TGTTCTAAGAGCTGG	1108
rs753167868	snp	A/G	1.72806e-05	0.00293938	intron-variant	CHD4	GRCh38.p7	12:6601915	TCTAGGAAACAAAAA[A/G]ACAAAAGTTTAACAG	1108
rs753175055	in-del	-/T			intron-variant	CHD4	GRCh38.p7	12:6574689	TAGTGGGAGGGGTGC[-/T]GATTTGTGAGAAATA	1108
rs753208619	in-del	-/AAA	0.00897049	0.0663685	intron-variant	CHD4	GRCh38.p7	12:6595957	GCAAGACTCCATCTC[-/AAA]AAAAAAAAAAAAGAA	1108
rs753226553	snp	A/G	0.000135623	0.00823366	intron-variant	CHD4	GRCh38.p7	12:6600050	CAGATTATTACCCCC[A/G]CCCGCCCACCGCAGT	1108
rs753240551	snp	A/G			missense	CHD4	GRCh38.p7	12:6598388	TGACCCCACTTCCAG[A/G]TTAGGATCTTCTGCA	1108
rs753312234	snp	C/T	1.65633e-05	0.00287774	intron-variant	CHD4	GRCh38.p7	12:6588271	ATAACATGTTACTTA[C/T]TAAGGCTGCCTGCTG	1108
rs753330768	in-del	-/ACACAC	1.65619e-05	0.00287762	intron-variant	CHD4	GRCh38.p7	12:6602208	GGAAGAGGGAGACAG[-/ACACAC]ACACACACATGCTAC	1108
rs753362164	in-del	-/ACACACAC			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607672	ACACCCCCCCCCCCA[-/ACACACAC]ACACACACACACACA	1108
rs753363556	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6597509	GGCTCACGCCTGTTA[A/C]TCCTAGCACTTAGGG	1108
rs753373346	snp	C/T	1.64914e-05	0.00287149	synonymous-codon	CHD4	GRCh38.p7	12:6578449	AAACATGAAACGTTG[C/T]TTAATATTTTTCTTC	1108
rs753381050	snp	C/T	1.65061e-05	0.00287277	intron-variant	CHD4	GRCh38.p7	12:6601547	TGGTGGAGAAATGCA[C/T]AAGAGCAGAGGGAAA	1108
rs753428770	snp	A/G	3.29832e-05	0.00406085	intron-variant	CHD4	GRCh38.p7	12:6573053	GCCGAATCGGCAGGA[A/G]GCAGGGGAGCCACTG	1108
rs753500180	snp	C/T	1.64789e-05	0.0028704	synonymous-codon	CHD4	GRCh38.p7	12:6595346	CACATCAACTGTTGG[C/T]GTTTCTGGAGGCCTC	1108
rs753501080	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6591393	ACACAGAAAAGGAGA[C/T]GCACAAGAAGTTACA	1108
rs753501216	in-del	-/TTC			intron-variant	CHD4	GRCh38.p7	12:6574226	TCTATAAAATGCTTT[-/TTC]TTCTCCCACTACATA	1108
rs753507739	snp	C/G	1.66029e-05	0.00288117	missense	CHD4	GRCh38.p7	12:6578092	TCATAAGTCTTCTTG[C/G]TAACTGTGGCTGCCC	1108
rs753555075	snp	A/T	1.64876e-05	0.00287116	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581611	ATAGGCCAGGACAAA[A/T]AGAGAGGGACAGAAA	1108
rs753567548	in-del	-/AAAA	1.72685e-05	0.00293836	intron-variant	CHD4	GRCh38.p7	12:6601910	AGGTGTCTAGGAAAC[-/AAAA]AGACAAAAGTTTAAC	1108
rs753574212	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	CHD4	GRCh38.p7	12:6599890	TTCCCCACCATCCTT[A/G]CAGACCCGACAGAAT	1108
rs753607968	snp	C/G	3.32033e-05	0.00407438	intron-variant	CHD4	GRCh38.p7	12:6578403	GTGGGCCCCTCATTT[C/G]CATACCAGTAAAACC	1108
rs753633533	snp	A/G			upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570326	AAATAAACCAACAAA[A/G]TAAAACCAAAAGGAG	1108
rs753699256	snp	C/G	1.6477e-05	0.00287024	intron-variant	CHD4	GRCh38.p7	12:6591859	AAAAAAGTATTAAAA[C/G]AAAGCCCACATGGAG	1108
rs753699412	snp	A/C	3.29788e-05	0.00406058	intron-variant	CHD4	GRCh38.p7	12:6595441	ACTCCCTAAAGAAGA[A/C]AGACATCACACAGCT	1108
rs753712557	snp	C/T	1.72113e-05	0.00293348	missense	CHD4	GRCh38.p7	12:6600948	CTCTTACGCTTGGAA[C/T]CAAAACCTCCCAGCT	1108
rs753743099	snp	A/G	3.29859e-05	0.00406102	intron-variant	CHD4	GRCh38.p7	12:6598139	CCACCAAGAAGCTGT[A/G]TTCATTCCTTCTATC	1108
rs753762151	in-del	-/AAGG	1.66366e-05	0.0028841	intron-variant	CHD4	GRCh38.p7	12:6578950	TTGAGACTATACCTA[-/AAGG]AAGGAAGAACATTCT	1108
rs753779789	snp	C/G	1.70936e-05	0.00292344	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582997	ACAAAGCAACATTTA[C/G]AAAAGCAACAAAAAA	1108
rs753811207	snp	C/T	3.29902e-05	0.00406128	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570649	AAGGTCACTGCTCAG[C/T]GGTGGAGGTGGTATC	1108
rs753831942	snp	C/T	3.29451e-05	0.00405851	missense	CHD4	GRCh38.p7	12:6602416	GGGATTTTAGGGTCC[C/T]GAGGTTTCTTAGGCT	1108
rs753850984	snp	A/G	4.95528e-05	0.00497734	synonymous-codon	CHD4	GRCh38.p7	12:6598252	CCAGGAGCAGTGCCA[A/G]TAAGACATGCCTTGC	1108
rs753851871	snp	A/G	3.42354e-05	0.00413721	intron-variant	CHD4	GRCh38.p7	12:6573276	TTCTAAGAGCTGGAC[A/G]AGGGATAAGAGGAAA	1108
rs753864818	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6584402	TGTGTACATATAAAT[A/C]TATATATATTTTTTT	1108
rs753889540	snp	C/T	5.00989e-05	0.00500469	intron-variant, upstream-variant-2KB, missense	CHD4, SCARNA11	GRCh38.p7	12:6583161	ACTGCTCTAGTGGAA[C/T]GGCCCATGGGTGGGG	1108
rs753973569	snp	A/G	9.88435e-05	0.00702937	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581196	GGAAAAAAAAACAAA[A/G]ACAAAACAGATGAAG	1108
rs754037034	snp	C/G	1.73126e-05	0.00294211	intron-variant	CHD4	GRCh38.p7	12:6601928	AAGACAAAAGTTTAA[C/G]AGTACAAAGAAGAGG	1108
rs754041262	snp	A/T	1.76574e-05	0.00297126	intron-variant	CHD4	GRCh38.p7	12:6594409	GTGTAAGTTAAGGCT[A/T]CAAACACAAAACACC	1108
rs754047047	snp	A/G	1.6495e-05	0.0028718	intron-variant	CHD4	GRCh38.p7	12:6577744	CGTTACGCACTTTCA[A/G]GTTTGTCACTTAAGC	1108
rs754073156	snp	A/C/G	3.30334e-05	0.00406397	intron-variant	CHD4	GRCh38.p7	12:6588292	CTGCCTGCTGCCTCT[A/C/G]CTCACCTGAATGTCA	1108
rs754085534	in-del	-/AAGG			intron-variant	CHD4	GRCh38.p7	12:6600401	CCTCCTCGCCTGGGC[-/AAGG]AAGGAAGAGGGAAAG	1108
rs754096136	snp	A/G	3.31538e-05	0.00407134	missense	CHD4	GRCh38.p7	12:6598361	CGAGGCACTGGTGTG[A/G]GAGATGGTGGCTGAC	1108
rs754097492	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6606093	CCGTGCCCAGGAGGC[A/C]CATGGCTTCCACCCC	1108
rs754150856	snp	A/G			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608233	AGCTCCACAGCCTAT[A/G]GTAAGTACCCCTCCT	1108
rs754152386	snp	A/G	1.73231e-05	0.002943	missense	CHD4	GRCh38.p7	12:6602009	TCCTCCTTCCGCTTG[A/G]ATTTGCTCTTCTTCT	1108
rs754171161	in-del	-/TAAAC			intron-variant	CHD4	GRCh38.p7	12:6590827	AGACCCTATCTCGAA[-/TAAAC]AAAACAAAACAGGCT	1108
rs754174255	in-del	-/CCAC			upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570171	CCTTTTTTTTTTTTT[-/CCAC]TTTATTTCATTTAGC	1108
rs754175682	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6574314	TTAATGCCCCATGAT[A/G]TGAATACATGTTTCA	1108
rs754200077	in-del	-/GAACTCATTCTCTCGGATGATGGCACGGC	1.648e-05	0.0028705	frameshift-variant	CHD4	GRCh38.p7	12:6593467	ATTGTCTTCAAAGGA[lengthTooLong]TGTCCTTGTCACCCA	1108
rs754229594	snp	C/T	8.23716e-05	0.00641709	synonymous-codon	CHD4	GRCh38.p7	12:6600334	ACCGCCTTGCTGGCA[C/T]ACCTCGCAATAGTCC	1108
rs754233554	snp	C/T	1.67503e-05	0.00289393	intron-variant	CHD4	GRCh38.p7	12:6591444	GAGGATTCCTGAAAC[C/T]AAACAACTCCTTCTC	1108
rs754269346	snp	A/C/G	9.0637e-05	0.00673137	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582121	TAGAAACAATGGCAA[A/C/G]AGGCTCAGGGCTCAC	1108
rs754279009	snp	G/T	1.64906e-05	0.00287142	missense	CHD4	GRCh38.p7	12:6578867	CTTCTACCACAATAG[G/T]GGTCAGATCTATTGC	1108
rs754281743	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6577366	CACAGAGGTTGTAGT[A/G]AGCAGAGGCTGCATC	1108
rs754322262	in-del	-/CCT			intron-variant	CHD4	GRCh38.p7	12:6595120	ATCATTCAAAATATA[-/CCT]CCTTTTTTTTTTTCT	1108
rs754354448	snp	A/G	1.67576e-05	0.00289457	intron-variant	CHD4	GRCh38.p7	12:6600487	GGAGATTCTTCCCCA[A/G]TCACTCCCACCTCAT	1108
rs754366858	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6605388	AGACATCTGCTTAGG[A/G]GCATGACATCAACCA	1108
rs754406645	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6588046	TTCAGTACAAGGCAA[A/G]GTCCACAGCCTACAT	1108
rs754440306	snp	G/T	3.29924e-05	0.00406142	synonymous-codon	CHD4	GRCh38.p7	12:6578856	CCCACCTTTGTCTTC[G/T]ACCACAATAGGGGTC	1108
rs754454493	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6574351	CATTCTCCTAATGCT[A/G]AACATTTATGTTGCC	1108
rs754460159	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6589138	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAAG	1108
rs754463324	snp	C/T	3.56303e-05	0.00422065	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582567	GAATGACCAGATAGA[C/T]AGCAGAAGCCCTTGC	1108
rs754471509	snp	A/G	1.65119e-05	0.00287327	intron-variant	CHD4	GRCh38.p7	12:6602545	GAAAAGATCAATAGC[A/G]AAAGGTTAGGCCCTA	1108
rs754493097	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6597269	TGACAAGTCTGTCTC[-/A]AAAAAAAACAATAAT	1108
rs754552051	in-del	-/A	1.76213e-05	0.00296822	intron-variant	CHD4	GRCh38.p7	12:6593665	GCCCCAGCACACTGC[-/A]ACCCCAGCGAACACC	1108
rs754586752	snp	A/G	1.66346e-05	0.00288393	intron-variant	CHD4	GRCh38.p7	12:6592062	TGTAGTATTTCCTAC[A/G]TGGGCAAGGTAGAAA	1108
rs754606238	snp	C/G	1.64773e-05	0.00287026	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583207	ACACACCTCGGTCCT[C/G]CTGGGAGCCATCATT	1108
rs754606685	snp	C/T	4.94279e-05	0.00497107	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581385	TCTATTTTTATCCCA[C/T]CTTCTGCAGAACAAT	1108
rs754677171	snp	A/G	1.64846e-05	0.0028709	missense	CHD4	GRCh38.p7	12:6570879	CCTACCTGCTGTGGG[A/G]TAGGTTCGGGTGCCC	1108
rs754857206	snp	G/T	3.42742e-05	0.00413955	missense	CHD4	GRCh38.p7	12:6602058	TCTTCTTCTTCTTCT[G/T]GCCAGGAGTATAGTC	1108
rs754880034	snp	C/T	1.64866e-05	0.00287106	missense	CHD4	GRCh38.p7	12:6594608	GCAGGGTTCCACCTG[C/T]AGCATCCAGGTACTC	1108
rs754883432	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6593849	CTTTATATACTTTTT[G/T]TCTGAGACGGAGTTT	1108
rs754886934	in-del	-/CC			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607661	AATACACACGGACAC[-/CC]CCCCCCCCAACACAC	1108
rs754888678	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6598680	TGGGCGTGGTGGCAT[G/T]CGCCTGTAGTCCCAG	1108
rs754911305	snp	A/G	3.31192e-05	0.00406921	synonymous-codon	CHD4	GRCh38.p7	12:6578055	GGCTAGCAGCCAGTA[A/G]TCATGCCGTCGATGC	1108
rs754990738	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6596344	CACCAGAATTCAGTC[A/T]GTTAATAATTAACAT	1108
rs755002159	snp	G/T	3.29609e-05	0.00405948	synonymous-codon	CHD4	GRCh38.p7	12:6577904	GGATGTCTTGCCACC[G/T]GGCATAGCCATGGCT	1108
rs755025675	snp	A/G	1.65844e-05	0.00287957	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582755	ACCAAGTACCTAGGG[A/G]AAGAAGAAACCCAGG	1108
rs755052654	snp	C/G	3.34225e-05	0.0040878	intron-variant	CHD4	GRCh38.p7	12:6600518	CCCATCACAAATATA[C/G]AGAAGAGAAACACAC	1108
rs755117437	snp	A/G			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582290	ATATGCCCTGTGTAA[A/G]GAAGTAGAGAAAGAG	1108
rs755147515	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6604834	TCCTGCGCAGCTCCC[A/G]GTCAACATGAAAGGC	1108
rs755158829	in-del	-/G	1.64765e-05	0.00287019	frameshift-variant	CHD4	GRCh38.p7	12:6587885	CCTCCACTGACGCAC[-/G]GGGTCACAAACCGGT	1108
rs755161099	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6603977	GCAGGACCTAGACAG[C/T]GGTAGAAGAGAATAT	1108
rs755191349	snp	C/T	3.40252e-05	0.00412449	missense	CHD4	GRCh38.p7	12:6606298	GTGGGGGCAGGCTGT[C/T]GTTCAAAAGTGCATC	1108
rs755212825	in-del	-/T	1.6495e-05	0.0028718	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581510	GAGCCAGCCCTATTC[-/T]TAGGACGGCCCTCCT	1108
rs755223600	snp	A/G	1.66228e-05	0.0028829	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582829	CACTCACCCCTCCTT[A/G]GAATCGTATGGCACT	1108
rs755247302	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6571133	TCAGTGACCAAGTAA[C/T]TGTGATGTATTGTCT	1108
rs755253497	snp	C/T	3.29658e-05	0.00405978	synonymous-codon	CHD4	GRCh38.p7	12:6597959	GCGATAGAAGCGTTC[C/T]TCCATCTCTGCAAAT	1108
rs755279634	snp	A/G	1.64982e-05	0.00287208	intron-variant	CHD4	GRCh38.p7	12:6587667	CTCCCTAACCTTTAG[A/G]GAGGCCAAGCCCCAC	1108
rs755289734	snp	A/G	1.64879e-05	0.00287118	synonymous-codon	CHD4	GRCh38.p7	12:6573093	GTGCAGGACTGCATT[A/G]GCTGGCTTGTTTCCT	1108
rs755300672	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6572245	AGCCTTGCCAACATG[C/G]TGAAACTCCATCTCT	1108
rs755349043	snp	C/G	1.702e-05	0.00291714	missense	CHD4	GRCh38.p7	12:6606341	CTCACTGCCCGCCGA[C/G]CAGGGGGACGGGGAG	1108
rs755360441	in-del	-/TTC			intron-variant	CHD4	GRCh38.p7	12:6574477	GAGGCAGAATGTTGG[-/TTC]TTAATTTATGAAAAG	1108
rs755376144	snp	A/G	3.32226e-05	0.00407556	intron-variant	CHD4	GRCh38.p7	12:6593370	AGGTAAACTAAGCCA[A/G]AAGCCACAACTCTTT	1108
rs755422385	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6596656	AATGCAAAAATTAGC[C/T]GGGCATGGTGGCAGG	1108
rs755444102	snp	A/G/T	3.41368e-05	0.00413128	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581709	GAGTGGAGGGTGTAG[A/G/T]AGTTTTTGGGGAGGG	1108
rs755447776	snp	A/C	1.65007e-05	0.00287229	missense	CHD4	GRCh38.p7	12:6593097	AGCCCTCACCTTAGA[A/C]TGATTGTTCTTCAGC	1108
rs755459447	snp	A/G	1.65051e-05	0.00287267	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581623	AAAAAGAGAGGGACA[A/G]AAAATGATAGGACAG	1108
rs755463952	snp	A/G	1.65119e-05	0.00287327	intron-variant	CHD4	GRCh38.p7	12:6598108	GCTCCAGCTTTGAGC[A/G]GAAAGAGAAAATCAG	1108
rs755471169	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6584916	GGTCGTTTCTGATTG[A/C]ACACTACGGTACACA	1108
rs755489323	snp	A/G	3.29468e-05	0.00405861	synonymous-codon	CHD4	GRCh38.p7	12:6601728	GTCAATGTCTTCCAT[A/G]CCCCAGTCTTCCAGG	1108
rs755495039	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6605678	CCTCCCCGAGCCCCC[A/G]TCACTTCCCCACTCA	1108
rs755519328	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6576877	TTAGTACATAATACC[C/T]GAAGGCTTATTAGTG	1108
rs755527057	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	CHD4	GRCh38.p7	12:6587833	CACCACTAGATGCGT[C/T]AGCATCATTTTCTTC	1108
rs755584570	snp	C/T	1.648e-05	0.0028705	missense	CHD4	GRCh38.p7	12:6570994	GTCGAGTCACATCAG[C/T]TTTCATGTCACTCAG	1108
rs755599397	snp	C/T	6.61037e-05	0.00574869	intron-variant	CHD4	GRCh38.p7	12:6587381	CCTTGGATTCATACT[C/T]ACCCCCATTTCTTCT	1108
rs755630059	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6585409	CTGCCTCAGCCTCCC[A/G]AATAGCTGGGACTAC	1108
rs755645884	snp	A/T	1.798e-05	0.00299827	intron-variant	CHD4	GRCh38.p7	12:6598459	ACTTAATCTCAAATC[A/T]TAACCATGGGAGGAG	1108
rs755655982	in-del	-/G	1.64784e-05	0.00287035	intron-variant	CHD4	GRCh38.p7	12:6601606	TAAGAAGAGAGAACA[-/G]AAAGATTCTCCTCCC	1108
rs755667676	snp	C/T	1.64887e-05	0.00287125	intron-variant	CHD4	GRCh38.p7	12:6577932	GCTATTGGAAAAGTG[C/T]TCAGGAAAAACAAAA	1108
rs755735901	snp	A/C	1.66527e-05	0.00288549	intron-variant	CHD4	GRCh38.p7	12:6601260	AGCCCACACTAGACA[A/C]CCCCACTCCCATTTG	1108
rs755755550	snp	C/T	0.000115461	0.00759718	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581511	AGCCAGCCCTATTCT[C/T]AGGACGGCCCTCCTA	1108
rs755799406	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6589623	AGTACAAAAATTAGC[C/T]GGGCGTGGTGGCGGG	1108
rs755840043	in-del	-/CTT	1.67153e-05	0.00289091	intron-variant	CHD4	GRCh38.p7	12:6596190	AGGCAACCCTCCTCA[-/CTT]CCTCTCAAAAACTGG	1108
rs755840734	snp	A/C/T	0.00013279	0.00814732	missense, intron-variant	CHD4	GRCh38.p7	12:6602174	CGGCATAAGAGCATA[A/C/T]GCTGGAGCAGGGCAA	1108
rs755848579	snp	C/T	3.30721e-05	0.00406632	intron-variant	CHD4	GRCh38.p7	12:6599739	AAAGACTACACTTTC[C/T]CATTTTTTGCCCCGG	1108
rs755855388	in-del	-/T	4.43017e-05	0.00470626	intron-variant	CHD4	GRCh38.p7	12:6578729	GGGACAGGTACAGTC[-/T]TTTTATCTTGGGATA	1108
rs755860786	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6590311	TCCTGAAACAGAAAA[C/T]AGACATCAAGAAAAA	1108
rs755937437	snp	G/T	1.65921e-05	0.00288024	missense	CHD4	GRCh38.p7	12:6578083	TGCCAGATCTCATAA[G/T]TCTTCTTGGTAACTG	1108
rs756003646	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6593329	CAGGGTTACCCTTTT[A/G]CCTCACCAGGGACCA	1108
rs756004986	snp	A/G	1.6599e-05	0.00288084	synonymous-codon	CHD4	GRCh38.p7	12:6594636	CTCTGGCTGTCGCTC[A/G]TACTTCACTGTTGGC	1108
rs756034955	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6600688	GCAGGATGAAAAAGA[A/G]TAAGGTTAGACGTTC	1108
rs756035048	snp	C/G	1.64749e-05	0.00287005	intron-variant	CHD4	GRCh38.p7	12:6602349	CTTCTTCCTCTGATT[C/G]CCCGTAACATTCAGT	1108
rs756038091	snp	A/G	1.64768e-05	0.00287021	intron-variant	CHD4	GRCh38.p7	12:6591847	ACAAATGCAAAGAAA[A/G]AAGTATTAAAAGAAA	1108
rs756049428	in-del	-/CA	3.30292e-05	0.00406368	intron-variant	CHD4	GRCh38.p7	12:6570848	AGGAAGAGGTGGTGT[-/CA]CAAGAAGAAAATGGT	1108
rs756129685	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6599635	ACAAAAGTATCCCAA[C/G]ACTATAGGATGAAGG	1108
rs756130125	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6595915	GTGAGTCAAGATCAC[A/G]CCACTGCACTACAGC	1108
rs756169368	snp	A/T	1.65012e-05	0.00287234	intron-variant	CHD4	GRCh38.p7	12:6598126	AAGAGAAAATCAGCC[A/T]CCAAGAAGCTGTGTT	1108
rs756171975	snp	A/G	1.64727e-05	0.00286986	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581122	CCTCTCCCTCAGGGG[A/G]TTCAACAACGACCTT	1108
rs756192147	snp	C/T	1.64947e-05	0.00287177	missense	CHD4	GRCh38.p7	12:6597993	GGGTCCTTGTTCTTT[C/T]GCTTTCGGCTTTTCT	1108
rs756243539	snp	A/G	1.64727e-05	0.00286986	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581100	ACCTCTGCCTTTTCC[A/G]CTTTCTCCTCTCCCT	1108
rs756259096	snp	A/C	6.7023e-05	0.00578852	intron-variant	CHD4	GRCh38.p7	12:6600721	GCCAAGGGGAAGGAC[A/C]GAGTGGCAGAGAGGG	1108
rs756269627	in-del	-/AT	1.64827e-05	0.00287073	frameshift-variant	CHD4	GRCh38.p7	12:6593452	GCCACCACGAATGGC[-/AT]TGTCTTCAAAGGAGA	1108
rs756282304	snp	C/G/T			intron-variant	CHD4	GRCh38.p7	12:6574292	TGAATTTTGTTGCTT[C/G/T]TGTTGTTTAATGCCC	1108
rs756282625	snp	A/G	5.06333e-05	0.00503131	synonymous-codon	CHD4	GRCh38.p7	12:6573267	CAGAGCTTGTTCTAA[A/G]AGCTGGACAAGGGAT	1108
rs756324936	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6593981	GCTGGGATTACAGGC[A/G]TGCACCACCACATCC	1108
rs756345156	snp	A/G	1.65004e-05	0.00287227	intron-variant	CHD4	GRCh38.p7	12:6601570	GAGGGAAAGGTTTAA[A/G]AATAAAAAAAGAAAG	1108
rs756370515	snp	A/C	1.6476e-05	0.00287014	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581187	CACTTCAAAGGAAAA[A/C]AAAACAAAAACAAAA	1108
rs756396113	snp	C/T	4.95381e-05	0.0049766	missense	CHD4	GRCh38.p7	12:6573106	TTGGCTGGCTTGTTT[C/T]CTGCCATTGACTCCT	1108
rs756411661	snp	C/T	6.63702e-05	0.00576027	intron-variant	CHD4	GRCh38.p7	12:6593385	GAAGCCACAACTCTT[C/T]CTCTAGGGTGGCTTC	1108
rs756431809	snp	C/T	1.70356e-05	0.00291848	intron-variant	CHD4	GRCh38.p7	12:6600060	CCCCCACCCGCCCAC[C/T]GCAGTCTGAAGCCAG	1108
rs756450902	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6577040	CTCCCGACTTCAAGC[A/G]ATTCTCCTGCATCAG	1108
rs756461519	in-del	-/AATTCATAAAT	1.69431e-05	0.00291055	intron-variant	CHD4	GRCh38.p7	12:6588469	TGTCTCCTAAATTCC[-/AATTCATAAAT]GTAGTTTAAAAAATT	1108
rs756524248	snp	C/G	1.65211e-05	0.00287407	intron-variant	CHD4	GRCh38.p7	12:6588288	AAGGCTGCCTGCTGC[C/G]TCTGCTCACCTGAAT	1108
rs756572071	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6604200	GAATCGCTTGAGCCC[A/G]GGAGGCGGAGGTTGC	1108
rs756583880	snp	C/T	4.89968e-05	0.00494934	intron-variant	CHD4	GRCh38.p7	12:6578695	AAATGGTGCCATTGG[C/T]CCACTGACAACTAAA	1108
rs756606295	snp	A/C	0.000115429	0.00759612	synonymous-codon	CHD4	GRCh38.p7	12:6593581	GATGATGGTAGAAAG[A/C]GGGGCGCTCACTAGG	1108
rs756612100	snp	A/G	1.65542e-05	0.00287695	synonymous-codon	CHD4	GRCh38.p7	12:6587941	AATCCGGTGAGCTCT[A/G]CTAAAGGCCTGGAGT	1108
rs756628084	snp	C/T	1.64746e-05	0.00287002	missense	CHD4	GRCh38.p7	12:6600290	ACCATGTGGTAAGCA[C/T]GGGGACAGGTATCAC	1108
rs756630032	snp	A/G	1.66205e-05	0.00288271	intron-variant	CHD4	GRCh38.p7	12:6595474	CCAAAATCCTTTTCT[A/G]TAGAAGAAACAACTT	1108
rs756644446	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6586663	TTGTGCCACTGCACT[C/T]TAGCCTGGGTGACAG	1108
rs756674376	snp	A/G	1.84869e-05	0.00304024	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582108	GCGCCTGGCCCCCTA[A/G]AAACAATGGCAAGAG	1108
rs756750413	snp	A/G	1.64993e-05	0.00287218	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581619	GGACAAAAAGAGAGG[A/G]ACAGAAAATGATAGG	1108
rs756753806	snp	G/T	3.30087e-05	0.00406242	intron-variant	CHD4	GRCh38.p7	12:6601555	AAATGCACAAGAGCA[G/T]AGGGAAAGGTTTAAG	1108
rs756823842	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6597564	AGGTCAGGAGTTCAA[C/G]ACCAGCCTGGCCAGC	1108
rs756887409	snp	C/T	1.64885e-05	0.00287123	missense	CHD4	GRCh38.p7	12:6578444	ATGTTAAACATGAAA[C/T]GTTGTTTAATATTTT	1108
rs756900931	snp	C/G	0.000482983	0.0155325	missense	CHD4	GRCh38.p7	12:6578105	TGGTAACTGTGGCTG[C/G]CCGCTCTTCATTCTG	1108
rs756910846	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6601909	AGGTGTCTAGGAAAC[-/A]AAAAAGACAAAAGTT	1108
rs756946348	snp	A/G	1.69867e-05	0.00291429	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581699	GTGTCCCCTGGAGTG[A/G]AGGGTGTAGGAGTTT	1108
rs756988356	snp	C/T			synonymous-codon	CHD4	GRCh38.p7	12:6578464	TTTAATATTTTTCTT[C/T]TGTTTCTCATCATTC	1108
rs757009605	snp	C/T	1.79178e-05	0.00299309	intron-variant	CHD4	GRCh38.p7	12:6600877	TAGAAGGTCACATCC[C/T]TTCTATTAGACATGG	1108
rs757035470	in-del	-/ACACACATGCT	0.000115945	0.00761308	intron-variant	CHD4	GRCh38.p7	12:6602211	AAGAGGGAGACAGAC[-/ACACACATGCT]ACACACATGCTGACC	1108
rs757054630	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6590414	ACTGCAGTTACGTAA[A/G]TTATTATTAAGAGAA	1108
rs757071483	snp	C/T	4.95626e-05	0.00497784	intron-variant	CHD4	GRCh38.p7	12:6592671	GGCACAATTATGAGC[C/T]GATTACAGATAAACA	1108
rs757085751	snp	A/C/G	1.64751e-05	0.00287007	synonymous-codon	CHD4	GRCh38.p7	12:6591934	TGCAGCCACAGGGAA[A/C/G]AGGTATGGATGGTTG	1108
rs757088917	snp	C/G	1.64776e-05	0.00287028	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581198	AAAAAAAAACAAAAA[C/G]AAAACAGATGAAGCA	1108
rs757174814	snp	A/G	1.7164e-05	0.00292945	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583000	AAGCAACATTTAGAA[A/G]AGCAACAAAAAAAGC	1108
rs757180954	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6605933	ACGCCCCCCTCCACC[A/C]CCACCACCACAAGCC	1108
rs757195889	snp	C/T	1.70898e-05	0.00292311	missense	CHD4	GRCh38.p7	12:6600955	GCTTGGAACCAAAAC[C/T]TCCCAGCTTGATTTT	1108
rs757201869	snp	C/T	1.64909e-05	0.00287144	intron-variant	CHD4	GRCh38.p7	12:6598146	GAAGCTGTGTTCATT[C/T]CTTCTATCCACAAGG	1108
rs757219464	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6589865	CACAAACCCAAACTT[A/T]AGAGACATTCTACAA	1108
rs757248416	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6572975	TCCTAAACTCCCAGA[A/C]AAAGGAGCTCTGAAA	1108
rs757337711	snp	A/G	1.65285e-05	0.00287471	missense	CHD4	GRCh38.p7	12:6593600	GCGCTCACTAGGAAG[A/G]GGCCTTTGGAATGAC	1108
rs757348405	snp	C/T	1.64961e-05	0.00287189	synonymous-codon	CHD4	GRCh38.p7	12:6593431	CTTCATGCGGGAGGC[C/T]TTCTTGCCACCACGA	1108
rs757358084	snp	A/G	1.64746e-05	0.00287002	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581301	CTTACCTCAATGGCA[A/G]TCTCAGGGGCTGTAG	1108
rs757432721	snp	C/G	1.90384e-05	0.00308526	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606406	CAGGGAATTGGCCCA[C/G]CTGCTCCTGCCGGCG	1108
rs757447870	snp	A/G			synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582643	CTGATTTGCCTCGCA[A/G]GTCTCTTACAAGCCA	1108
rs757499258	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6601203	CTATCTCCTACCTTA[C/G]GGCTGACAGACCAGC	1108
rs757516960	snp	C/G	1.6486e-05	0.00287102	missense	CHD4	GRCh38.p7	12:6596052	CGTAATCCTGGATCT[C/G]CACATCCTCACTCTC	1108
rs757529523	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6594952	TAAATAATCGTTATG[G/T]CCCTCTTAGATTCAT	1108
rs757541932	snp	C/G	1.73246e-05	0.00294312	intron-variant	CHD4	GRCh38.p7	12:6601942	ACAGTACAAAGAAGA[C/G]GATGGAGGTCCAGGC	1108
rs757571981	in-del	-/G	1.68764e-05	0.00290481	intron-variant	CHD4	GRCh38.p7	12:6595966	ATCTCAAAAAAAAAA[-/G]AAAAAGAAACAACTC	1108
rs757582624	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6596256	ATGCCACAGATCACA[C/T]GTTTTCAGAGCCTCT	1108
rs757595830	snp	A/C/T	0.000117287	0.00765714	intron-variant	CHD4	GRCh38.p7	12:6600496	TCCCCAATCACTCCC[A/C/T]CCTCATCCCATCACA	1108
rs757686666	snp	A/G	9.56526e-05	0.00691499	intron-variant	CHD4	GRCh38.p7	12:6578716	GACAACTAAATGTGG[A/G]GACAGGTACAGTCTT	1108
rs757727388	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6572580	TTTTTTTTCTGGAGT[C/T]TCACTATGTTGCCCA	1108
rs757749902	in-del	-/A	1.64741e-05	0.00286998	intron-variant	CHD4	GRCh38.p7	12:6591671	CTATGACTGTTCCCT[-/A]AAGCTCCCAGTCCAC	1108
rs757765922	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6588994	GACTCACACCTGTAA[A/C]CCCAACACTTTGCGA	1108
rs757766116	snp	G/T	1.64961e-05	0.00287189	synonymous-codon	CHD4	GRCh38.p7	12:6592472	CATCGGCTTTGAGCC[G/T]CCGCAACATGTGCGG	1108
rs757768167	in-del	-/A	3.34647e-05	0.00409038	intron-variant	CHD4	GRCh38.p7	12:6593623	GAATGACCCTTTGAG[-/A]AAAAAAGAGGAGAGT	1108
rs757775899	snp	A/C	1.74187e-05	0.00295111	intron-variant	CHD4	GRCh38.p7	12:6606224	GAGGAGTCACTCGGG[A/C]GAGCCCCAGATGTCT	1108
rs757777183	snp	A/C	3.29468e-05	0.00405861	intron-variant	CHD4	GRCh38.p7	12:6602371	ACATTCAGTCACCCA[A/C]TCACCTCCTTTTTTT	1108
rs757789818	snp	G/T	1.66735e-05	0.00288729	intron-variant	CHD4	GRCh38.p7	12:6596184	CAGAAAAGGCAACCC[G/T]CCTCACTTCCTCTCA	1108
rs757822229	snp	C/T	3.30814e-05	0.00406689	intron-variant	CHD4	GRCh38.p7	12:6595458	GACATCACACAGCTG[C/T]CCAAAATCCTTTTCT	1108
rs757830186	snp	A/G	1.81223e-05	0.00301012	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581852	TGAAGACCCAATTCC[A/G]GCTACAGGCTCCTTT	1108
rs757879181	snp	C/T	1.64901e-05	0.00287137	missense	CHD4	GRCh38.p7	12:6578876	CAATAGGGGTCAGAT[C/T]TATTGCTGACTTTTC	1108
rs757958176	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6587036	ACCAGAAAACACAAA[A/G]AGATAGATTACCTAG	1108
rs757968523	snp	A/C	1.69172e-05	0.00290832	intron-variant	CHD4	GRCh38.p7	12:6600047	ATTCAGATTATTACC[A/C]CCACCCGCCCACCGC	1108
rs757969490	snp	A/T	1.79123e-05	0.00299263	intron-variant	CHD4	GRCh38.p7	12:6600883	GTCACATCCTTTCTA[A/T]TAGACATGGCACCCT	1108
rs757988546	snp	A/C	1.64735e-05	0.00286993	synonymous-codon	CHD4	GRCh38.p7	12:6595370	AGGCCTCTCCAACTT[A/C]CGAAGCTTCACCTTC	1108
rs758014481	snp	C/T	1.65512e-05	0.00287669	missense	CHD4	GRCh38.p7	12:6592013	CCACCACCTCGGGCA[C/T]TGAGTGCTTCAAAAT	1108
rs758024959	in-del	-/A			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608044	AATAGTCAGAAACTC[-/A]CCCCCCCCCATACTA	1108
rs758062681	snp	C/T	1.74394e-05	0.00295286	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583015	AAGCAACAAAAAAAG[C/T]ACAGCCCTCACCTTC	1108
rs758067982	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6580584	TGGTGGTACATGCCT[A/G]TAATCCCAGCTACTC	1108
rs758073736	snp	A/G	4.99696e-05	0.00499823	intron-variant	CHD4	GRCh38.p7	12:6578954	AGACTATACCTAAAG[A/G]AAGAACATTCTCCTC	1108
rs758074090	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6598577	GCACCTTGGGAGGCC[A/G]AGGCGGGCAGATCAC	1108
rs758077820	snp	A/G	3.58551e-05	0.00423394	intron-variant	CHD4	GRCh38.p7	12:6601100	CAAGACCAAAGATGG[A/G]GAAAATAAAATCTTC	1108
rs758086869	snp	C/G	1.68264e-05	0.0029005	intron-variant	CHD4	GRCh38.p7	12:6578685	CAGACCCAGAAAATG[C/G]TGCCATTGGCCCACT	1108
rs758136003	snp	A/G	8.25266e-05	0.00642312	missense	CHD4	GRCh38.p7	12:6598316	TCCAAGGGCTTTGGG[A/G]AGGGCGTGTTGGGAT	1108
rs758173093	in-del	-/AT	3.29462e-05	0.00405857	intron-variant	CHD4	GRCh38.p7	12:6591687	AAGCTCCCAGTCCAC[-/AT]GATACCTGGGAAAAG	1108
rs758199479	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6605927	TCCTCAACGCCCCCC[C/T]CCACCACCACCACCA	1108
rs758210504	snp	C/T	1.64796e-05	0.00287046	intron-variant	CHD4	GRCh38.p7	12:6577778	ATATTCCTCCCCAAC[C/T]GCTCACCTTAAACCT	1108
rs758250094	snp	A/G	1.69746e-05	0.00291325	synonymous-codon	CHD4	GRCh38.p7	12:6601016	CTTGGCATCAGGTAC[A/G]CGAGGGCTGCCCTTG	1108
rs758257024	snp	A/G	1.64773e-05	0.00287026	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581219	AGATGAAGCAGACAG[A/G]CCAGCAACTAAAAGG	1108
rs758272043	snp	A/C	1.68145e-05	0.00289948	missense	CHD4	GRCh38.p7	12:6598396	CTTCCAGATTAGGAT[A/C]TTCTGCACTTTGCCC	1108
rs758274687	snp	A/G	1.69525e-05	0.00291135	synonymous-codon	CHD4	GRCh38.p7	12:6592404	TCACTTCTGCATAGG[A/G]CTCAGCTCCACACGC	1108
rs758309532	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6603808	CTCAGTGGACTTGTG[A/G]TCAGCGCATACAACC	1108
rs758332449	snp	A/G	1.67058e-05	0.00289009	intron-variant	CHD4	GRCh38.p7	12:6593622	TGGAATGACCCTTTG[A/G]GAAAAAAGAGGAGAG	1108
rs758389446	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6577561	CCCCTCTGCACTAGT[A/G]TGTCACTGATTGGAC	1108
rs758439369	snp	A/G	1.64743e-05	0.00287	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581317	TCTCAGGGGCTGTAG[A/G]TTTAACCTCCTTTTC	1108
rs758469357	snp	C/T	1.65952e-05	0.00288051	intron-variant	CHD4	GRCh38.p7	12:6591460	AAACAACTCCTTCTC[C/T]CTCACCATTGAAGCG	1108
rs758479656	in-del	-/C			upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570170	CCTTTTTTTTTTTTT[-/C]CCACTTTATTTCATT	1108
rs758495195	snp	C/T	3.30671e-05	0.00406602	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582703	TACCATATCGCATAA[C/T]TGCATTAAGAAAGGC	1108
rs758499850	snp	A/G	1.64776e-05	0.00287028	missense	CHD4	GRCh38.p7	12:6577880	GGATGGCATAGCGTG[A/G]GTCATTCTGGATGTC	1108
rs758510882	snp	A/C	1.64912e-05	0.00287147	synonymous-codon, intron-variant	CHD4	GRCh38.p7	12:6600382	ACCATCCACAGCAGT[A/C]ACCTCCTCCTCGCCT	1108
rs758596073	snp	A/G	0.000138629	0.00832438	intron-variant	CHD4	GRCh38.p7	12:6601956	AGGATGGAGGTCCAG[A/G]CACCTTTGAATCATC	1108
rs758638879	snp	A/G	1.65045e-05	0.00287263	missense	CHD4	GRCh38.p7	12:6578905	TCCTCCACCTTCTCT[A/G]CATCAGCAGCACCTA	1108
rs758665490	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6584583	GAGACGGAATTTTAC[A/C]ATGTTGCCCAAGTTG	1108
rs758680304	snp	A/G	1.7741e-05	0.00297829	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582586	AGAAGCCCTTGCTCT[A/G]GATCAGTCCACTCCA	1108
rs758691484	snp	A/G	3.40507e-05	0.00412604	synonymous-codon	CHD4	GRCh38.p7	12:6606293	GTGGGGTGGGGGCAG[A/G]CTGTTGTTCAAAAGT	1108
rs758702410	snp	A/C	8.36617e-05	0.00646714	intron-variant	CHD4	GRCh38.p7	12:6600509	CCACCTCATCCCATC[A/C]CAAATATACAGAAGA	1108
rs758815436	in-del	-/AAAC	4.45206e-05	0.00471787	intron-variant	CHD4	GRCh38.p7	12:6595973	AAAAAAAAAAAAAAG[-/AAAC]AACTCTATGCCTCAC	1108
rs758838598	snp	A/G/T	0.00013211	0.00812644	intron-variant	CHD4	GRCh38.p7	12:6587611	TTTCAGCAGCTGCAG[A/G/T]GGAAAAAGCAAGTCC	1108
rs758857965	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6596590	GGATCACCTGAGGTC[A/G]GGAGTTCAAGACCAG	1108
rs758921938	snp	C/T	1.64779e-05	0.00287031	synonymous-codon	CHD4	GRCh38.p7	12:6601347	AGGGGGAGGTGGTGG[C/T]GCAACCTCAGTGGCT	1108
rs758925273	snp	A/C	3.30726e-05	0.00406635	splice-donor-variant, missense	CHD4	GRCh38.p7	12:6573073	GGGAGCCACTGGCTA[A/C]CTTTGTGCAGGACTG	1108
rs758929074	snp	A/G	0.000131776	0.00811608	synonymous-codon	CHD4	GRCh38.p7	12:6587491	CCTGGTTACGGTCTA[A/G]CAGCCGTTCAATGGC	1108
rs758972353	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6591213	TTTGAGCTTGAACAA[C/G]TCCTGACCCTTTGCT	1108
rs759024138	snp	C/T	1.65037e-05	0.00287256	synonymous-codon	CHD4	GRCh38.p7	12:6571010	TTTCATGTCACTCAG[C/T]AGTTCTTCCAGCTGT	1108
rs759024692	snp	A/G	1.65905e-05	0.0028801	intron-variant	CHD4	GRCh38.p7	12:6596173	ACCCTCAGAGCCAGA[A/G]AAGGCAACCCTCCTC	1108
rs759042451	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6574866	GGAGTTGGCAAGCTA[C/T]AGCCTGTGGGCCAGA	1108
rs759045712	snp	A/C			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569954	CATACTGCACCCACA[A/C]ACAGAACCCAGTTAC	1108
rs759051352	in-del	-/AAC			intron-variant	CHD4	GRCh38.p7	12:6580229	AGACTCCATCTCGAA[-/AAC]AACAACAACAACAAC	1108
rs759061062	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6601905	CAGTAAGGTGTCTAG[C/G]AAACAAAAAGACAAA	1108
rs759155947	snp	C/T	1.67195e-05	0.00289127	missense	CHD4	GRCh38.p7	12:6602109	GCAGAGCCACCTCTT[C/T]CTCCTCCTCCACAAA	1108
rs759182221	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6583835	AAAGCTTACCAACTG[C/T]CTGCAGAACGAAAAG	1108
rs759190742	snp	A/C	3.29462e-05	0.00405857	missense	CHD4	GRCh38.p7	12:6570946	TCTGTAACCTCACAG[A/C]AACTGGGGGAATTCG	1108
rs759218992	snp	C/T	1.648e-05	0.0028705	missense	CHD4	GRCh38.p7	12:6597907	ACCTGTGGTTGAGGA[C/T]TCGGTGGATCATCAT	1108
rs759250013	in-del	-/TCT	0.000149469	0.00864363	cds-indel	CHD4	GRCh38.p7	12:6578525	ATCACCTCTTTTTTC[-/TCT]TCTTCTTCTTTCTTC	1108
rs759263592	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6595663	CATGGTGGCAGACGC[C/T]TGTAATCTCAGCTAC	1108
rs759264991	snp	A/G	1.65258e-05	0.00287448	intron-variant	CHD4	GRCh38.p7	12:6592647	AAATGGGCAACAGGA[A/G]GAATGAGAGGCACAA	1108
rs759267211	snp	A/C/T	0.00029684	0.0121795	intron-variant	CHD4	GRCh38.p7	12:6573045	TCAGGGAGGCCGAAT[A/C/T]GGCAGGAGGCAGGGG	1108
rs759286393	snp	A/T			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569748	AACTAACATTAAGGT[A/T]GTGGTTAGGTGTTAA	1108
rs759356507	snp	A/G	1.64901e-05	0.00287137	missense	CHD4	GRCh38.p7	12:6601498	ATCATCTTGGAGACA[A/G]CAATCTTGGGATTTT	1108
rs759375934	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6574762	ACTGCTCCCTCTCTT[C/T]TTAAATGACAATTTA	1108
rs759444267	snp	G/T	1.64806e-05	0.00287054	missense	CHD4	GRCh38.p7	12:6601336	GGCACCTCCACAGGG[G/T]GAGGTGGTGGTGCAA	1108
rs759471021	snp	C/G	1.67019e-05	0.00288975	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581664	CAGCAGGTGGGACAG[C/G]TGCAGGAGTGTTGGG	1108
rs759494401	snp	C/T	4.97294e-05	0.0049862	intron-variant	CHD4	GRCh38.p7	12:6602220	ACAGACACACACATG[C/T]TACACACATGCTGAC	1108
rs759504268	snp	C/T	1.64776e-05	0.00287028	synonymous-codon	CHD4	GRCh38.p7	12:6595424	TTCCTCACCCCTCAT[C/T]AACTCCCTAAAGAAG	1108
rs759544747	snp	A/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607844	CATCCTTTGCCAACT[A/T]CTTCTTCACTCTTGG	1108
rs759559001	snp	C/T	1.64806e-05	0.00287054	intron-variant	CHD4	GRCh38.p7	12:6587700	CAAAACGTAAGTTCC[C/T]GACTACCTCACCTCC	1108
rs759584456	snp	A/C	1.64768e-05	0.00287021	intron-variant	CHD4	GRCh38.p7	12:6591839	TCCTGAGAACAAATG[A/C]AAAGAAAAAAGTATT	1108
rs759585087	snp	C/G/T	4.94338e-05	0.00497141	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581591	GAGCACAGGGGAGCA[C/G/T]AAAAATAGGCCAGGA	1108
rs759596308	snp	A/G	1.64741e-05	0.00286998	synonymous-codon	CHD4	GRCh38.p7	12:6599977	CTCACCCTCCGAATT[A/G]TCCTCTTTAGCTTCC	1108
rs759610469	in-del	-/AG	1.66952e-05	0.00288917	intron-variant	CHD4	GRCh38.p7	12:6592858	AAATCCAATGAAAAC[-/AG]AGCTCTAGCAAATCT	1108
rs759692528	snp	A/G	3.32862e-05	0.00407946	intron-variant	CHD4	GRCh38.p7	12:6600711	AGACGTTCAAGCCAA[A/G]GGGAAGGACAGAGTG	1108
rs759695732	snp	G/T	1.70766e-05	0.00292199	intron-variant	CHD4	GRCh38.p7	12:6578185	GGGGAAGCAAACATC[G/T]GTGAGAATTGAAAAA	1108
rs759722348	snp	A/C	3.29837e-05	0.00406088	intron-variant	CHD4	GRCh38.p7	12:6595323	CTACAGTCCCTTCCA[A/C]CCCCACTCACATCAA	1108
rs759763778	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6598197	TCATCGTAGCCCCTA[C/T]ATCTCCAGACTATCC	1108
rs759778622	snp	C/G	0.000197664	0.00993947	intron-variant	CHD4	GRCh38.p7	12:6591899	CCCAGGGAGGAACAG[C/G]AGATGGCACTACATA	1108
rs759816295	snp	C/T	1.6473e-05	0.00286988	missense	CHD4	GRCh38.p7	12:6602395	TTTTTTTGGCGCTTG[C/T]TCTTAGGGATTTTAG	1108
rs759824473	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6587602	CAAAGTCAGTTTCAG[C/T]AGCTGCAGTGGAAAA	1108
rs759846450	snp	C/T			synonymous-codon	CHD4	GRCh38.p7	12:6601299	TTCACCTTTGCCCTC[C/T]TTGGTCTTGGCCTTG	1108
rs759889190	snp	C/G/T	0.000513239	0.0160127	intron-variant, upstream-variant-2KB, missense	CHD4, SCARNA11	GRCh38.p7	12:6583138	GAGAGGGCAGATGAG[C/G/T]GGGGCCCACTGCTCT	1108
rs759898622	snp	C/T	3.31895e-05	0.00407353	synonymous-codon	CHD4	GRCh38.p7	12:6578521	AAGCATCACCTCTTT[C/T]TTCTCTTCTTCTTCT	1108
rs759905990	snp	A/G	1.78963e-05	0.00299129	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606392	CTTCCGCTCCCGGCC[A/G]GGGAATTGGCCCAGC	1108
rs759917417	snp	C/T	1.94177e-05	0.00311584	intron-variant	CHD4	GRCh38.p7	12:6573315	CGACTGATAACTCAC[C/T]TTACTCACTTCTGAC	1108
rs759940656	snp	G/T	1.64765e-05	0.00287019	splice-acceptor-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581175	GGGGCCTGTGTACAC[G/T]TCAAAGGAAAAAAAA	1108
rs759961615	snp	C/T	1.65688e-05	0.00287821	intron-variant	CHD4	GRCh38.p7	12:6598200	TCGTAGCCCCTACAT[C/T]TCCAGACTATCCTAA	1108
rs760012522	snp	C/G	1.77944e-05	0.00298276	intron-variant	CHD4	GRCh38.p7	12:6600912	CTCCCTAAAGCGATG[C/G]GCTGGGCTCTCACCG	1108
rs760063868	snp	C/T	1.71684e-05	0.00292983	intron-variant	CHD4	GRCh38.p7	12:6593651	AGTCAGGACTGAGGG[C/T]CCCAGCACACTGCAA	1108
rs760072068	in-del	-/C	1.66421e-05	0.00288458	frameshift-variant	CHD4	GRCh38.p7	12:6602147	CCTCCCCAGAGCTGT[-/C]CCCCCAGCTGCCGGC	1108
rs760111195	snp	A/G	3.30082e-05	0.00406239	synonymous-codon	CHD4	GRCh38.p7	12:6592461	GTTCTTGAACACATC[A/G]GCTTTGAGCCGCCGC	1108
rs760111468	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6578599	AAAGCCCAGCACCAT[C/T]GCCCTTACCCAGAAC	1108
rs760115343	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6578288	ACAGAACCCACTATC[A/T]GTTTGGCATTCCCTC	1108
rs760117748	in-del	-/TC			intron-variant	CHD4	GRCh38.p7	12:6574164	TTTTTAAAAACTGTT[-/TC]TGTTTCCTATGTATG	1108
rs760135213	snp	A/T	1.66283e-05	0.00288338	synonymous-codon	CHD4	GRCh38.p7	12:6573246	GCGCAGCTGTTCCTC[A/T]ATCACCAGAGCTTGT	1108
rs760146680	snp	A/T	1.66366e-05	0.0028841	intron-variant	CHD4	GRCh38.p7	12:6593046	ATTGGTAGTACTAGA[A/T]AAAACCCAAAGTGGG	1108
rs760156045	snp	C/T	1.65162e-05	0.00287365	missense	CHD4	GRCh38.p7	12:6598332	AGGGCGTGTTGGGAT[C/T]AGCATCTGGAGGCCG	1108
rs760188215	snp	A/G	1.70356e-05	0.00291848	synonymous-codon	CHD4	GRCh38.p7	12:6606329	CATATCCTCCTCCTC[A/G]CTGCCCGCCGAGCAG	1108
rs760200517	snp	G/T	1.65165e-05	0.00287367	missense	CHD4	GRCh38.p7	12:6598083	TTTCGGAACATCACC[G/T]GACAGTGCAGCTCCA	1108
rs760202761	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6591287	AAATACCCCAAAAGA[A/G]AAAATCTCCTAGGAA	1108
rs760215670	snp	A/G	1.64795e-05	0.00287045	missense	CHD4	GRCh38.p7	12:6573181	AAGCGGGTGTTGAGG[A/G]CCATGGAAGGGTGAG	1108
rs760254559	snp	A/C	1.7318e-05	0.00294256	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606374	CAGGCCCGACGCCAT[A/C]CCCTTCCGCTCCCGG	1108
rs760265171	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	CHD4	GRCh38.p7	12:6587734	AGTGGCTTCATCCTT[A/G]AATAGTTCCTCAGTG	1108
rs760270237	snp	C/T	1.64741e-05	0.00286998	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581068	CTGTCTCCATAGGTT[C/T]CTCTGTTCTCTCCTT	1108
rs760272876	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6603255	ACACACAAAGCCTGG[C/G]TAAGACTGAAAGCTC	1108
rs760286352	snp	A/G	1.65474e-05	0.00287636	intron-variant	CHD4	GRCh38.p7	12:6600672	CATCATCCTCACTCT[A/G]GCAGGATGAAAAAGA	1108
rs760291708	in-del	-/T	1.6478e-05	0.00287032	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581191	CAAAGGAAAAAAAAA[-/T]CAAAAACAAAACAGA	1108
rs760304205	snp	A/C			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6570060	ATCCACCTGCACCTA[A/C]ACCCACACTGAACCA	1108
rs760334309	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6597610	TCTCTACTAAAAATA[C/G]AAAAAATTAGCTGGG	1108
rs760341012	snp	C/G	1.66056e-05	0.00288141	missense	CHD4	GRCh38.p7	12:6593218	ACATGGAATTTCACA[C/G]ATGCCTCTTTCTGCA	1108
rs760379924	in-del	-/T	1.80305e-05	0.00300249	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582334	ATGCTGACTCTTAGA[-/T]TCTTTTCCATCCCTT	1108
rs760383433	snp	A/G	3.37234e-05	0.00410616	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581684	GGAGTGTTGGGCTGC[A/G]TGTCCCCTGGAGTGG	1108
rs760392657	snp	A/G	1.65059e-05	0.00287275	missense	CHD4	GRCh38.p7	12:6601529	TGGCAGCAATGAGGG[A/G]TCTGGTGGAGAAATG	1108
rs760447679	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6585273	AGAAGGGAGGAGAAT[A/G]AAAAGGTATATACCG	1108
rs760521781	snp	A/G	1.6483e-05	0.00287076	missense	CHD4	GRCh38.p7	12:6599999	TTAGCTTCCCACTGG[A/G]TGCCTTCCTTCTCCT	1108
rs760552787	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6584295	TATACACATAAAATA[G/T]TTTTGGAAAGATATA	1108
rs760583470	snp	C/G	1.67928e-05	0.0028976	intron-variant	CHD4	GRCh38.p7	12:6578370	ACCCCAATTTCACAT[C/G]AGATCCTTCTAACCC	1108
rs760603056	snp	A/G	1.6473e-05	0.00286988	intron-variant	CHD4	GRCh38.p7	12:6591910	ACAGGAGATGGCACT[A/G]CATACCATTGCAGCC	1108
rs760621559	snp	C/T	1.6786e-05	0.00289702	intron-variant	CHD4	GRCh38.p7	12:6578557	CTCTTCTACAGAATA[C/T]GGGGAAGAAAAATGT	1108
rs760628620	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6576249	GTTGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	1108
rs760630244	snp	A/C	0.00680712	0.0579416	intron-variant	CHD4	GRCh38.p7	12:6595976	AAAAAAAAAAAGAAA[A/C]AACTCTATGCCTCAC	1108
rs760665384	snp	C/G	1.79281e-05	0.00299394	intron-variant	CHD4	GRCh38.p7	12:6592342	AATAGGAAACACTCT[C/G]CAGACTGGCAGATGT	1108
rs760683009	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6597008	AGTGCGGCGGCTCAC[A/G]CCTGTAATCCCAGCA	1108
rs760693230	snp	C/T	1.64882e-05	0.00287121	synonymous-codon	CHD4	GRCh38.p7	12:6602490	CTCTTCTGGGTCCTC[C/T]TCATTTTCTACATAT	1108
rs760698915	snp	C/T	1.74096e-05	0.00295034	missense	CHD4	GRCh38.p7	12:6600939	ACCGAGGATCTCTTA[C/T]GCTTGGAACCAAAAC	1108
rs760796350	snp	A/G	1.69775e-05	0.0029135	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582987	AGGATATTAAACAAA[A/G]CAACATTTAGAAAAG	1108
rs760804594	snp	C/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607557	GCAACCCCCGCCCCC[C/T]CGTCGCTCAGGCAAC	1108
rs760839505	snp	A/G	1.64762e-05	0.00287016	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581273	TTTAGTATGGCATTC[A/G]GTCACCCCATCTCTT	1108
rs760848532	snp	G/T	1.69778e-05	0.00291352	intron-variant, upstream-variant-2KB, synonymous-codon	CHD4, SCARNA11	GRCh38.p7	12:6583142	GGGCAGATGAGCGGG[G/T]CCCACTGCTCTAGTG	1108
rs760849000	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6584237	GTCTTTGGGTACATA[C/T]ATGTGAGTGTACATA	1108
rs760852905	snp	A/G	3.29902e-05	0.00406128	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570637	GAGAAAGTGAGGAAG[A/G]TCACTGCTCAGCGGT	1108
rs760854708	in-del	-/T			intron-variant	CHD4	GRCh38.p7	12:6586705	TCTCTTTTTTTGTTG[-/T]TTTTTTTTTTTCAAA	1108
rs760875213	in-del	-/AAAC			intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581008	ACACTGTCTCAAAAC[-/AAAC]AAACAAACAAACAAA	1108
rs760891971	snp	A/G			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608203	GCTCACATCACCCCC[A/G]GCCTTCCCTCTTCTA	1108
rs760895026	snp	A/G	5.26727e-05	0.00513163	intron-variant	CHD4	GRCh38.p7	12:6601063	TGGGACCTAAAATCA[A/G]GATATATCCAAATAT	1108
rs760904570	snp	C/T	1.68343e-05	0.00290118	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583354	CTTCCTGTTTAATGA[C/T]TTCCCGTTCTACCTC	1108
rs760968221	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6587996	TGTATTTTCCTGGTG[C/T]CACTCTTATCCTGAC	1108
rs760971489	in-del	-/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607970	TAATATTCAGCCCCA[-/T]TCCCCCACAGACATC	1108
rs760978874	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6605955	CCACAAGCCTCCAGG[A/G]GTCCCAGCTACCTGC	1108
rs761003853	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6575063	TTATTCATTTATGTA[C/T]CCCCTGTGGCTGCTT	1108
rs761036067	snp	C/G	1.64833e-05	0.00287078	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581436	GAAGGTACTAGATCA[C/G]AGAGAAGGTCATTTC	1108
rs761061164	snp	A/G	1.72856e-05	0.00293982	intron-variant	CHD4	GRCh38.p7	12:6601919	GGAAACAAAAAGACA[A/G]AAGTTTAACAGTACA	1108
rs761071214	snp	C/T	1.74042e-05	0.00294988	intron-variant	CHD4	GRCh38.p7	12:6593662	AGGGCCCCAGCACAC[C/T]GCAACCCCAGCGAAC	1108
rs761102450	snp	C/G	1.73546e-05	0.00294568	missense	CHD4	GRCh38.p7	12:6602004	CCTCCTCCTCCTTCC[C/G]CTTGGATTTGCTCTT	1108
rs761106624	snp	A/G	1.64784e-05	0.00287035	synonymous-codon	CHD4	GRCh38.p7	12:6594528	CATCTCATCAGCCAA[A/G]ATGGTGTCAGTGCCC	1108
rs761162911	snp	A/G	1.65266e-05	0.00287455	missense	CHD4	GRCh38.p7	12:6598347	CAGCATCTGGAGGCC[A/G]AGGCACTGGTGTGGG	1108
rs761229855	snp	A/G	3.29522e-05	0.00405894	missense	CHD4	GRCh38.p7	12:6577865	TGAAAGGCTCATTGA[A/G]GATGGCATAGCGTGG	1108
rs761265027	snp	C/G	0.000970775	0.0220101	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606418	CCAGCTGCTCCTGCC[C/G]GCGGCCTGAGGACCT	1108
rs761303485	snp	C/T	1.64727e-05	0.00286986	missense	CHD4	GRCh38.p7	12:6587787	GCTCCTGTTTGGACA[C/T]AGATCCAGTCTTGGA	1108
rs761356709	snp	A/C	3.50773e-05	0.00418777	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606380	CGACGCCATCCCCTT[A/C]CGCTCCCGGCCAGGG	1108
rs761364563	snp	A/G			synonymous-codon	CHD4	GRCh38.p7	12:6592719	CTCGGGGGTGAGAAA[A/G]TTGAGCAGATGAAAC	1108
rs761393792	snp	C/T	1.80742e-05	0.00300612	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581814	GTTCAAACTCCTGAA[C/T]CTGTAGCAATGGGAC	1108
rs761412156	snp	C/G	1.64827e-05	0.00287073	missense	CHD4	GRCh38.p7	12:6573200	TGGAAGGGTGAGAAG[C/G]GTCTTCTGACATGTT	1108
rs761477668	snp	A/C	1.64727e-05	0.00286986	synonymous-codon	CHD4	GRCh38.p7	12:6602418	GATTTTAGGGTCCCG[A/C]GGTTTCTTAGGCTTT	1108
rs761494434	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6591396	CAGAAAAGGAGATGC[A/G]CAAGAAGTTACAGTC	1108
rs761507020	snp	C/T	1.69919e-05	0.00291473	intron-variant	CHD4	GRCh38.p7	12:6578596	GCCAAAGCCCAGCAC[C/T]ATCGCCCTTACCCAG	1108
rs761527068	snp	A/T	1.65422e-05	0.0028759	intron-variant	CHD4	GRCh38.p7	12:6600019	TTCCTTCTCCTGCAG[A/T]AAAGGACCACAGATT	1108
rs761570351	snp	A/G	1.65853e-05	0.00287964	synonymous-codon	CHD4	GRCh38.p7	12:6600217	TGGCCAGACACTCAC[A/G]CAGTGTGGGCAGCTC	1108
rs761571811	snp	A/G	1.65792e-05	0.00287912	intron-variant	CHD4	GRCh38.p7	12:6588256	CTATGCCTTTCTAGC[A/G]TAACATGTTACTTAT	1108
rs761615091	in-del	-/G	1.66e-05	0.00288092	intron-variant, upstream-variant-2KB, frameshift-variant	CHD4, SCARNA11	GRCh38.p7	12:6583173	GAACGGCCCATGGGT[-/G]GGGGGCGGGGCCGGC	1108
rs761649929	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6585332	CTCTGTCCCCCAGGC[C/T]GGAGTGCAGTGGGGC	1108
rs761666793	snp	A/C	1.64727e-05	0.00286986	intron-variant	CHD4	GRCh38.p7	12:6595986	AGAAACAACTCTATG[A/C]CTCACCCAAAATCAC	1108
rs761705137	snp	G/T	1.64942e-05	0.00287173	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570653	TCACTGCTCAGCGGT[G/T]GAGGTGGTATCAGTC	1108
rs761707961	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6595293	CAGCAAAGATACATT[G/T]TCCTACCCAACAAAC	1108
rs761725960	in-del	-/TTT	3.29478e-05	0.00405867	cds-indel, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581354	TATGCTCTCTTCTTC[-/TTT]GAGGCTATTTTCCTC	1108
rs761755684	snp	A/G	3.33417e-05	0.00408286	intron-variant, upstream-variant-2KB, missense	CHD4, SCARNA11	GRCh38.p7	12:6583162	CTGCTCTAGTGGAAC[A/G]GCCCATGGGTGGGGG	1108
rs761797551	snp	C/G	3.55233e-05	0.00421431	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583407	AGGGCCAGGACTCAG[C/G]AGTGCTGAAGTCAGC	1108
rs761827386	snp	G/T	1.64963e-05	0.00287192	intron-variant	CHD4	GRCh38.p7	12:6602509	TTTTCTACATATATT[G/T]GGCAAAGAGTGGTAG	1108
rs761840545	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6597785	CAAAAAACAAACAAA[A/G]AAAACCAGTGTCTTC	1108
rs761855550	snp	C/T	3.31862e-05	0.00407333	synonymous-codon	CHD4	GRCh38.p7	12:6598366	CACTGGTGTGGGAGA[C/T]GGTGGCTGACCCCAC	1108
rs761855632	snp	C/G	3.30071e-05	0.00406232	synonymous-codon	CHD4	GRCh38.p7	12:6601293	CCCCATTTCACCTTT[C/G]CCCTCCTTGGTCTTG	1108
rs761861412	snp	C/T	0.000124421	0.00788639	intron-variant	CHD4	GRCh38.p7	12:6592363	TGGCAGATGTCTAAA[C/T]GGAGTCTGCTTCTGT	1108
rs761881455	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6572972	ACCTCCTAAACTCCC[-/A]GACAAAGGAGCTCTG	1108
rs761945521	snp	A/C	1.77957e-05	0.00298287	intron-variant	CHD4	GRCh38.p7	12:6601084	ATCCAAATATATACC[A/C]CAAGACCAAAGATGG	1108
rs761948882	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607372	CTCCTCGCCGCGGCC[C/G]AAGGGGGGAAAATGG	1108
rs761972899	snp	A/C	3.52156e-05	0.00419602	intron-variant	CHD4	GRCh38.p7	12:6594418	AAGGCTTCAAACACA[A/C]AACACCCACACAAAA	1108
rs761984548	snp	A/C/G	3.29534e-05	0.00405904	missense	CHD4	GRCh38.p7	12:6577876	TTGAGGATGGCATAG[A/C/G]GTGGGTCATTCTGGA	1108
rs761993543	snp	C/T	1.64879e-05	0.00287118	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581456	AAGGTCATTTCTTCC[C/T]AGTTTGTCTCATCTT	1108
rs761996529	in-del	-/GAAGGA	6.66067e-05	0.00577052	intron-variant	CHD4	GRCh38.p7	12:6600714	CGTTCAAGCCAAGGG[-/GAAGGA]CAGAGTGGCAGAGAG	1108
rs762018108	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6590184	ATCTGGGCAACAGAG[A/T]GAGACTCCATCCCGA	1108
rs762031121	in-del	-/TCC	0.00444772	0.0469476	cds-indel	CHD4	GRCh38.p7	12:6601978	GAATCATCATCATCA[-/TCC]TCCTCCTCCTCCTCC	1108
rs762033904	snp	A/G	1.64754e-05	0.00287009	missense	CHD4	GRCh38.p7	12:6594560	GAGCCCAGGAGAAGC[A/G]CAACCAATTCAGGCC	1108
rs762042290	snp	C/T	1.6477e-05	0.00287024	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581563	TGTCCTGCCAGACTA[C/T]CCTGTTAGAACTGAG	1108
rs762049705	snp	A/T	1.65773e-05	0.00287895	intron-variant	CHD4	GRCh38.p7	12:6599723	CAATAGCCTACATAG[A/T]AAAGACTACACTTTC	1108
rs762101468	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6575291	CATCTCTACTAAAAA[C/T]ACAAAAATTAGTCAG	1108
rs762121638	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6590960	AACCACATCTCTACT[-/A]AAAAATACAAAAATT	1108
rs762151199	in-del	-/TT			upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570157	CTTTTGGTTTTTTCC[-/TT]TTTTTTTTTTTTTCC	1108
rs762168617	snp	A/G	1.65201e-05	0.00287398	intron-variant	CHD4	GRCh38.p7	12:6577984	ACTAAAAGACCTTCA[A/G]AACCTTTCACCAAAA	1108
rs762228597	snp	A/G	1.65899e-05	0.00288005	synonymous-codon	CHD4	GRCh38.p7	12:6600568	GGTTCGGAGTTTCTT[A/G]CGGCTGCGGCTACTA	1108
rs762231502	snp	C/G	1.64882e-05	0.00287121	intron-variant	CHD4	GRCh38.p7	12:6591610	GCACGGTTTAATTAT[C/G]GAAGAGTCAGATGGT	1108
rs762251135	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6601620	AGAAAGATTCTCCTC[C/T]CCCTTCCCCAAACCC	1108
rs762273432	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	CHD4	GRCh38.p7	12:6591766	CAGCAGCAATAATTT[C/T]CCAGATGCTCTGATT	1108
rs762312908	snp	C/T	1.73045e-05	0.00294142	synonymous-codon	CHD4	GRCh38.p7	12:6602020	CTTGGATTTGCTCTT[C/T]TTCTCTTTCTTAGGT	1108
rs762332246	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6589167	AGAGAATAGCTTGAA[A/C]CCGGGAGGCAGAAGT	1108
rs762348120	in-del	-/G	0.00010067	0.00709401	intron-variant	CHD4	GRCh38.p7	12:6578168	GGGAAGGTTGGGGGT[-/G]GGGGGAAGCAAACAT	1108
rs762363905	snp	C/T	3.3232e-05	0.00407614	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582809	ACCAAAGATGCAATA[C/T]CTGACACTCACCCCT	1108
rs762364248	snp	C/T	0.000100013	0.00707083	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6580998	GCGGCAGCACTACAC[C/T]GTCTCAAAACAAACA	1108
rs762401869	snp	C/G/T	5.19821e-05	0.00509792	missense	CHD4	GRCh38.p7	12:6602001	CCTCCTCCTCCTCCT[C/G/T]CCGCTTGGATTTGCT	1108
rs762485123	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6583664	TTCTAACCCCTTGCA[C/T]TGATGCATATACAAT	1108
rs762516346	snp	A/G	5.18211e-05	0.00508998	intron-variant	CHD4	GRCh38.p7	12:6601911	GGTGTCTAGGAAACA[A/G]AAAGACAAAAGTTTA	1108
rs762521962	snp	C/T	3.37353e-05	0.00410689	intron-variant	CHD4	GRCh38.p7	12:6591420	TACAGTCCAAAGATA[C/T]AAGCAAATGAGGATT	1108
rs762601008	snp	A/G	1.66167e-05	0.00288237	intron-variant	CHD4	GRCh38.p7	12:6600429	AAGCCCAGTTATTGG[A/G]AAAAAACTACCTCCC	1108
rs762628767	snp	A/G	1.6651e-05	0.00288535	intron-variant	CHD4	GRCh38.p7	12:6592597	GGAAAAAAGTTATTG[A/G]AGAAGGAGAAAGGAA	1108
rs762673415	snp	A/C	0.000132767	0.00814652	intron-variant	CHD4	GRCh38.p7	12:6595992	AACTCTATGCCTCAC[A/C]CAAAATCACTCACCT	1108
rs762678951	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6605598	AAAAAAGCCAAAACT[A/G]TGTCCACTCACCAGG	1108
rs762705764	snp	G/T	1.76166e-05	0.00296783	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582299	GTGTAAAGAAGTAGA[G/T]AAAGAGTTAAATAGG	1108
rs762738200	snp	A/G	1.65121e-05	0.00287329	intron-variant	CHD4	GRCh38.p7	12:6570850	GGAAGAGGTGGTGTC[A/G]AGAAGAAAATGGTCC	1108
rs762740101	snp	A/G	1.65784e-05	0.00287905	intron-variant	CHD4	GRCh38.p7	12:6578932	CCTAGGGGAAGAAAT[A/G]TTATTGAGACTATAC	1108
rs762788560	snp	A/G	3.42079e-05	0.00413555	missense	CHD4	GRCh38.p7	12:6606276	GGGAAGATGTTACCT[A/G]GGTGGGGTGGGGGCA	1108
rs762883120	snp	A/G	1.65021e-05	0.00287241	intron-variant	CHD4	GRCh38.p7	12:6602530	AGAGTGGTAGGCAGG[A/G]AAAAGATCAATAGCA	1108
rs762910084	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6604770	CAGGAATGGGGTGTG[A/G]CAAGTGGAAAAAGTG	1108
rs762921522	snp	A/G	3.29462e-05	0.00405857	synonymous-codon	CHD4	GRCh38.p7	12:6599806	CCATTCACCGTTGGG[A/G]ATCTCTGGAAGTGGG	1108
rs762922027	snp	C/T	1.64912e-05	0.00287147	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581470	CCAGTTTGTCTCATC[C/T]TAAATTGTCCTCTCG	1108
rs762923906	snp	C/T	1.64928e-05	0.00287161	intron-variant	CHD4	GRCh38.p7	12:6587583	AATCAAGGGCCCACA[C/T]CCCCAAAGTCAGTTT	1108
rs762932920	snp	A/G	3.295e-05	0.00405881	synonymous-codon	CHD4	GRCh38.p7	12:6570911	GTTTGCCAGGCGGCT[A/G]AGAATGTTACGCTCT	1108
rs762951792	snp	A/C	1.64822e-05	0.00287068	missense	CHD4	GRCh38.p7	12:6601325	CCTTGCGGATAGGCA[A/C]CTCCACAGGGGGAGG	1108
rs762958878	in-del	-/A	4.95201e-05	0.0049757	intron-variant	CHD4	GRCh38.p7	12:6587666	CTCCCTAACCTTTAG[-/A]AGAGGCCAAGCCCCA	1108
rs762970816	snp	A/C	1.66651e-05	0.00288657	intron-variant	CHD4	GRCh38.p7	12:6587354	TCAGACCAATTACCA[A/C]GCACAGGATTGCCTT	1108
rs762972496	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6572014	GCCTGTAGTCCCAGC[C/T]ACTCAGGAGGCTGAG	1108
rs762986039	snp	C/G	1.64765e-05	0.00287019	synonymous-codon	CHD4	GRCh38.p7	12:6594573	GCGCAACCAATTCAG[C/G]CCCTCCATTTGATAG	1108
rs763010037	snp	C/G	3.29484e-05	0.00405871	synonymous-codon	CHD4	GRCh38.p7	12:6601446	TTTGAAGGGGTTATT[C/G]GTACTGAACTCCCGC	1108
rs763013320	snp	A/G	1.671e-05	0.00289045	intron-variant	CHD4	GRCh38.p7	12:6587335	TTGGTCTCAATGCCA[A/G]TTTTCAGACCAATTA	1108
rs763025549	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6573587	TAGAAATACATCCTG[A/C]TATTTTTCTTTTTAG	1108
rs763048375	in-del	-/AAGA	1.66391e-05	0.00288431	intron-variant	CHD4	GRCh38.p7	12:6592611	GGAGAAGGAGAAAGG[-/AAGA]AAGAAAAGTGATACA	1108
rs763108838	snp	A/T	1.64743e-05	0.00287	missense	CHD4	GRCh38.p7	12:6591797	AGGGCACTGCCATCA[A/T]ACATGCCATTAGGCA	1108
rs763117525	snp	A/G/T	6.59071e-05	0.00574021	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581583	TTAGAACTGAGCACA[A/G/T]GGGAGCAGAAAAATA	1108
rs763149491	snp	A/C	1.65699e-05	0.00287831	intron-variant	CHD4	GRCh38.p7	12:6599728	GCCTACATAGAAAAG[A/C]CTACACTTTCCCATT	1108
rs763189593	snp	A/G	1.64947e-05	0.00287177	intron-variant	CHD4	GRCh38.p7	12:6577945	TGCTCAGGAAAAACA[A/G]AACAAGGAAAGTAAG	1108
rs763190508	snp	A/G	1.6793e-05	0.00289763	intron-variant	CHD4	GRCh38.p7	12:6578171	AAGGTTGGGGGTGGG[A/G]GGAAGCAAACATCTG	1108
rs763190555	in-del	-/GAA			intron-variant	CHD4	GRCh38.p7	12:6605311	TAAACTAGAAAACAT[-/GAA]GGTCAAGGAGATGAG	1108
rs763196929	snp	A/T	3.30109e-05	0.00406256	intron-variant	CHD4	GRCh38.p7	12:6595309	TCCTACCCAACAAAC[A/T]ACAGTCCCTTCCACC	1108
rs763207937	in-del	-/CTT	5.19679e-05	0.00509718	cds-indel	CHD4	GRCh38.p7	12:6601999	CTCCTCCTCCTCCTC[-/CTT]CCGCTTGGATTTGCT	1108
rs763244223	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6587982	ATAAAGCCAGAAATT[G/T]TATTTTCCTGGTGCC	1108
rs763306773	snp	C/T	1.66272e-05	0.00288328	intron-variant	CHD4	GRCh38.p7	12:6593246	GCACATGAAGGCAAC[C/T]TGGTCACTACTAGTC	1108
rs763316829	snp	A/C	1.64738e-05	0.00286995	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581164	AGGCAGGGGCAGGGG[A/C]CTGTGTACACTTCAA	1108
rs763338895	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6585017	ATCACAGGTAAGCAT[C/G]AGGGAAACACAGCAA	1108
rs763359336	snp	C/T	0.000116352	0.00762642	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582820	AATATCTGACACTCA[C/T]CCCTCCTTAGAATCG	1108
rs763398552	snp	A/G	1.65143e-05	0.00287348	intron-variant	CHD4	GRCh38.p7	12:6598104	TGCAGCTCCAGCTTT[A/G]AGCGGAAAGAGAAAA	1108
rs763407178	snp	C/T	1.67086e-05	0.00289033	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582965	AAGATGAATGAGTGA[C/T]ACAGGTAGGATATTA	1108
rs763441048	snp	A/C/G	3.31281e-05	0.00406978	intron-variant	CHD4	GRCh38.p7	12:6602213	GAGGGAGACAGACAC[A/C/G]CACATGCTACACACA	1108
rs763477403	snp	C/T	1.65858e-05	0.00287969	missense	CHD4	GRCh38.p7	12:6600572	CGGAGTTTCTTGCGG[C/T]TGCGGCTACTACGGC	1108
rs763493841	snp	C/T	1.65641e-05	0.00287781	intron-variant	CHD4	GRCh38.p7	12:6598192	CCTCTTCATCGTAGC[C/T]CCTACATCTCCAGAC	1108
rs763513049	snp	C/T	1.70374e-05	0.00291863	missense	CHD4	GRCh38.p7	12:6606331	TATCCTCCTCCTCAC[C/T]GCCCGCCGAGCAGGG	1108
rs763546688	snp	A/G	1.65097e-05	0.00287308	intron-variant	CHD4	GRCh38.p7	12:6587609	AGTTTCAGCAGCTGC[A/G]GTGGAAAAAGCAAGT	1108
rs763553335	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6602993	TAACCACTTTGAAGT[A/C]ATCACTGCTCAAATT	1108
rs763562083	snp	A/G	0.000280716	0.0118439	synonymous-codon	CHD4	GRCh38.p7	12:6598088	GAACATCACCTGACA[A/G]TGCAGCTCCAGCTTT	1108
rs763586448	in-del	-/C	1.66543e-05	0.00288563	intron-variant	CHD4	GRCh38.p7	12:6601259	AGCCCACACTAGACA[-/C]CCCCCACTCCCATTT	1108
rs763640224	snp	A/C/G	4.978e-05	0.00498878	intron-variant	CHD4	GRCh38.p7	12:6593063	AAACCCAAAGTGGGG[A/C/G]CTCCAACATCCCTCC	1108
rs763677195	snp	A/G	0.000382114	0.013817	intron-variant	CHD4	GRCh38.p7	12:6573052	GGCCGAATCGGCAGG[A/G]GGCAGGGGAGCCACT	1108
rs763681137	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6591370	AATGACAAAGTCCCA[A/G]AAGAACTACACAGAA	1108
rs763710115	in-del	-/GGGA	1.65732e-05	0.00287859	intron-variant	CHD4	GRCh38.p7	12:6602192	GGAGCAGGGCAAGGG[-/GGGA]GGGAAGAGGGAGACA	1108
rs763716407	snp	A/T	1.65059e-05	0.00287275	intron-variant	CHD4	GRCh38.p7	12:6601535	CAATGAGGGGTCTGG[A/T]GGAGAAATGCACAAG	1108
rs763733474	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6603402	ACCCCCGCCCAAAGG[A/G]GGGTGGGTAGAGAAA	1108
rs763742420	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	CHD4	GRCh38.p7	12:6587739	CTTCATCCTTGAATA[A/G]TTCCTCAGTGCCAAA	1108
rs763763367	snp	C/T	1.64912e-05	0.00287147	missense	CHD4	GRCh38.p7	12:6571005	TCAGCTTTCATGTCA[C/T]TCAGCAGTTCTTCCA	1108
rs763767059	snp	C/T	1.64738e-05	0.00286995	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581080	GTTCCTCTGTTCTCT[C/T]CTTCACCTCTGCCTT	1108
rs763808934	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6592139	AACAACTGAGATCTT[C/T]CTTCCAACACATCCC	1108
rs763810511	snp	A/C	1.64727e-05	0.00286986	synonymous-codon	CHD4	GRCh38.p7	12:6599872	GGTATCACAGCAGAG[A/C]AGTTCCCCACCATCC	1108
rs763846015	in-del	-/AA	1.6487e-05	0.0028711	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581193	AAAGGAAAAAAAAAC[-/AA]AAACAAAACAGATGA	1108
rs763848358	snp	C/T	3.61239e-05	0.00424978	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581806	ATTAACATGTTCAAA[C/T]TCCTGAACCTGTAGC	1108
rs763918604	snp	C/G	0.000267009	0.0115513	intron-variant	CHD4	GRCh38.p7	12:6578387	GATCCTTCTAACCCT[C/G]GTGGGCCCCTCATTT	1108
rs763948065	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6585288	AAAAAGGTATATACC[A/G]ATTCTAATCTTTTTG	1108
rs763955970	snp	C/T	1.65299e-05	0.00287483	missense	CHD4	GRCh38.p7	12:6573229	TTCAAGTAAGCAGCC[C/T]GGCGCAGCTGTTCCT	1108
rs763962246	snp	A/G	3.35948e-05	0.00409833	intron-variant	CHD4	GRCh38.p7	12:6578561	TCTACAGAATATGGG[A/G]AAGAAAAATGTCAGC	1108
rs763993576	snp	A/C	1.64727e-05	0.00286986	synonymous-codon	CHD4	GRCh38.p7	12:6602415	AGGGATTTTAGGGTC[A/C]CGAGGTTTCTTAGGC	1108
rs764000588	snp	A/C	1.65263e-05	0.00287452	intron-variant	CHD4	GRCh38.p7	12:6600016	GCCTTCCTTCTCCTG[A/C]AGTAAAGGACCACAG	1108
rs764004840	snp	A/G	3.29582e-05	0.00405931	synonymous-codon	CHD4	GRCh38.p7	12:6595337	ACCCCCACTCACATC[A/G]ACTGTTGGCGTTTCT	1108
rs764010606	snp	C/T	1.68618e-05	0.00290356	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581685	GAGTGTTGGGCTGCG[C/T]GTCCCCTGGAGTGGA	1108
rs764072833	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6594891	GGAAAAGCACGTCAC[A/G]GACTCCCTACCAATA	1108
rs764087741	snp	C/T	1.64743e-05	0.00287	intron-variant	CHD4	GRCh38.p7	12:6602352	CTTCCTCTGATTCCC[C/T]GTAACATTCAGTCAC	1108
rs764120768	snp	A/C	1.6478e-05	0.00287032	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581191	TCAAAGGAAAAAAAA[A/C]CAAAAACAAAACAGA	1108
rs764123901	in-del	-/TCT	1.65015e-05	0.00287237	cds-indel	CHD4	GRCh38.p7	12:6578851	AAACACCCACCTTTG[-/TCT]TCTACCACAATAGGG	1108
rs764130358	snp	G/T	1.706e-05	0.00292057	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582994	TAAACAAAGCAACAT[G/T]TAGAAAAGCAACAAA	1108
rs764178833	snp	C/G	3.30934e-05	0.00406763	missense	CHD4	GRCh38.p7	12:6598232	CTTACCTGCAGTTCA[C/G]AAACCCAGGAGCAGT	1108
rs764194364	snp	C/G	1.72746e-05	0.00293888	synonymous-codon	CHD4	GRCh38.p7	12:6600944	GGATCTCTTACGCTT[C/G]GAACCAAAACCTCCC	1108
rs764195378	snp	C/T	1.67391e-05	0.00289297	intron-variant, upstream-variant-2KB, missense	CHD4, SCARNA11	GRCh38.p7	12:6583156	GGCCCACTGCTCTAG[C/T]GGAACGGCCCATGGG	1108
rs764262355	snp	C/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608229	TTCTAGCTCCACAGC[C/T]TATAGTAAGTACCCC	1108
rs764272928	snp	C/T	1.79338e-05	0.00299443	intron-variant	CHD4	GRCh38.p7	12:6592343	ATAGGAAACACTCTG[C/T]AGACTGGCAGATGTC	1108
rs764314849	snp	C/T	1.6476e-05	0.00287014	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581278	TATGGCATTCAGTCA[C/T]CCCATCTCTTACCTC	1108
rs764323007	in-del	-/AGAT			intron-variant	CHD4	GRCh38.p7	12:6605818	AAGCTAAAAATAATC[-/AGAT]AGAGTGTAACCAGCA	1108
rs764350470	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6606043	CTGGGAACTGCAGAG[A/C]ATTCCTCAAGACAGA	1108
rs764371903	snp	A/T	1.72844e-05	0.00293971	intron-variant	CHD4	GRCh38.p7	12:6601920	GAAACAAAAAGACAA[A/T]AGTTTAACAGTACAA	1108
rs764373303	snp	A/G	3.29837e-05	0.00406088	synonymous-codon	CHD4	GRCh38.p7	12:6593584	GATGGTAGAAAGAGG[A/G]GCGCTCACTAGGAAG	1108
rs764383019	in-del	-/AC			intron-variant	CHD4	GRCh38.p7	12:6605490	TGAAGCCACCCCAAA[-/AC]ACAGATAGCGTAACC	1108
rs764414531	snp	C/T	3.55511e-05	0.00421596	intron-variant	CHD4	GRCh38.p7	12:6593668	CCAGCACACTGCAAC[C/T]CCAGCGAACACCCAC	1108
rs764421286	snp	A/G	1.64762e-05	0.00287016	synonymous-codon	CHD4	GRCh38.p7	12:6577866	GAAAGGCTCATTGAG[A/G]ATGGCATAGCGTGGG	1108
rs764425345	snp	A/G	0.000117528	0.00766485	intron-variant	CHD4	GRCh38.p7	12:6587998	TATTTTCCTGGTGCC[A/G]CTCTTATCCTGACTT	1108
rs764487357	in-del	-/A/AA/AAA	0.51794	0.101081	intron-variant	CHD4	GRCh38.p7	12:6595956	GCAAGACTCCATCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA	1108
rs764490880	in-del	-/AGA	9.88891e-05	0.00703099	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581439	GGTACTAGATCAGAG[-/AGA]AGGTCATTTCTTCCC	1108
rs764502808	in-del	-/TCTTCAA	1.64822e-05	0.00287068	frameshift-variant	CHD4	GRCh38.p7	12:6593456	CCACGAATGGCATTG[-/TCTTCAA]AGGAGAACTCATTCT	1108
rs764506106	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6600081	CTGAAGCCAGTGCCC[A/C]TCATTCCTTTGAATG	1108
rs764594317	snp	C/G	0.000100035	0.0070716	intron-variant	CHD4	GRCh38.p7	12:6600037	AGGACCACAGATTCA[C/G]ATTATTACCCCCACC	1108
rs764598745	snp	A/C/G/T	0.000281769	0.0118665	intron-variant	CHD4	GRCh38.p7	12:6588259	TGCCTTTCTAGCATA[A/C/G/T]CATGTTACTTATTAA	1108
rs764668500	snp	A/C/G	3.30892e-05	0.00406739	intron-variant	CHD4	GRCh38.p7	12:6601815	CACCTAGTGCCCACA[A/C/G]TTGCTAAGCAAATTT	1108
rs764706475	snp	A/G	1.6476e-05	0.00287014	missense	CHD4	GRCh38.p7	12:6593526	CATAGGTTACGACAT[A/G]CATGTCTGGAGCCCA	1108
rs764782051	in-del	-/AC	6.62712e-05	0.00575597	intron-variant	CHD4	GRCh38.p7	12:6602222	AGACACACACATGCT[-/AC]ACACATGCTGACCTC	1108
rs764790056	snp	A/G	1.64963e-05	0.00287192	intron-variant	CHD4	GRCh38.p7	12:6595446	CTAAAGAAGAAAGAC[A/G]TCACACAGCTGCCCA	1108
rs764861587	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6599277	TCTCAACAGAGATTT[C/T]TTTTTTTTAATTAGC	1108
rs764866504	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6591316	AATAGTCCAATACAT[C/T]CGTCCAATTGAGACA	1108
rs764871171	snp	C/T	1.80811e-05	0.00300669	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581824	CTGAACCTGTAGCAA[C/T]GGGACAAGAAGTTGA	1108
rs764906304	snp	A/G	1.64846e-05	0.0028709	missense	CHD4	GRCh38.p7	12:6573211	GAAGGGTCTTCTGAC[A/G]TGTTCAAGTAAGCAG	1108
rs764937999	snp	C/T	1.65523e-05	0.00287678	synonymous-codon	CHD4	GRCh38.p7	12:6600223	GACACTCACGCAGTG[C/T]GGGCAGCTCCACTTG	1108
rs764940961	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6578678	TGTCTCTCAGACCCA[G/T]AAAATGGTGCCATTG	1108
rs764984608	snp	A/C	3.31884e-05	0.00407346	intron-variant	CHD4	GRCh38.p7	12:6578814	GGTTTTAGAGTTCTT[A/C]TGAACCACAATCAAC	1108
rs764988979	snp	A/C/G	1.6869e-05	0.00290417	intron-variant	CHD4	GRCh38.p7	12:6591422	CAGTCCAAAGATATA[A/C/G]GCAAATGAGGATTCC	1108
rs765010849	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6603661	ACAGTTCACAAGAGC[C/T]CACCCTAACATCCTA	1108
rs765052129	snp	C/T	1.78086e-05	0.00298396	intron-variant	CHD4	GRCh38.p7	12:6601085	TCCAAATATATACCA[C/T]AAGACCAAAGATGGG	1108
rs765064264	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6604504	TGGGAATGCAACATC[A/G]GCCTGGATTTCACCA	1108
rs765074116	snp	G/T	8.71878e-05	0.00660199	intron-variant	CHD4	GRCh38.p7	12:6578667	CTCCACCTGGGTGTC[G/T]CTCAGACCCAGAAAA	1108
rs765089487	snp	C/T	1.64727e-05	0.00286986	missense	CHD4	GRCh38.p7	12:6602425	GGGTCCCGAGGTTTC[C/T]TAGGCTTTTTCTTCT	1108
rs765113864	in-del	-/T	1.66032e-05	0.0028812	intron-variant	CHD4	GRCh38.p7	12:6587368	AAGCACAGGATTGCC[-/T]TGGATTCATACTCAC	1108
rs765159128	in-del	-/CAAT	1.64789e-05	0.0028704	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581407	CAGAACAATAAAAGA[-/CAAT]CAATTAGGAAGAAGG	1108
rs765170017	snp	C/T	1.64765e-05	0.00287019	synonymous-codon	CHD4	GRCh38.p7	12:6591940	CACAGGGAAGAGGTA[C/T]GGATGGTTGCAGCAC	1108
rs765180452	snp	C/G			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569982	TACTCAGTGGGGTAT[C/G]AGGACACCACGTAGC	1108
rs765180803	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6603176	AGCTGTCACCATCTC[C/G]CCTACACCCGCCCCC	1108
rs765213185	snp	G/T	1.68618e-05	0.00290356	synonymous-codon	CHD4	GRCh38.p7	12:6600974	CAGCTTGATTTTCAG[G/T]GGAGCTACTTTCTTG	1108
rs765233730	snp	A/G	5.28062e-05	0.00513812	intron-variant	CHD4	GRCh38.p7	12:6594419	AGGCTTCAAACACAA[A/G]ACACCCACACAAAAA	1108
rs765233874	snp	A/G	1.65767e-05	0.00287891	intron-variant	CHD4	GRCh38.p7	12:6599724	AATAGCCTACATAGA[A/G]AAGACTACACTTTCC	1108
rs765276010	snp	G/T	4.99355e-05	0.00499652	intron-variant	CHD4	GRCh38.p7	12:6592592	AAAAAGGAAAAAAGT[G/T]ATTGGAGAAGGAGAA	1108
rs765295381	snp	A/G	1.64741e-05	0.00286998	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581308	CAATGGCAGTCTCAG[A/G]GGCTGTAGATTTAAC	1108
rs765319548	snp	A/C	3.32773e-05	0.00407892	missense	CHD4	GRCh38.p7	12:6598376	GGAGATGGTGGCTGA[A/C]CCCACTTCCAGATTA	1108
rs765356530	snp	C/T			synonymous-codon	CHD4	GRCh38.p7	12:6598285	TTTCACAAAGAACTG[C/T]CGCTCTGGCCGCCCC	1108
rs765396565	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6597309	AATAAATAAAGATAA[C/T]AACATGAAGTGTCAG	1108
rs765428027	snp	C/T	1.64754e-05	0.00287009	synonymous-codon	CHD4	GRCh38.p7	12:6594561	AGCCCAGGAGAAGCG[C/T]AACCAATTCAGGCCC	1108
rs765476033	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6584485	GCTCACTGCAGCCTC[A/G]ACTGCCAAGTTTAAG	1108
rs765480799	snp	C/T	3.30382e-05	0.00406423	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582683	AAAAGCATCCTGAGG[C/T]GGCATACCATATCGC	1108
rs765487334	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6596371	ACATAGAGTGTTGGC[C/T]GGGTGCAGTGGCTCA	1108
rs765522797	in-del	-/CCTA			intron-variant	CHD4	GRCh38.p7	12:6601194	TCCTCCCTCCTATCT[-/CCTA]CCTTAGGGCTGACAG	1108
rs765530207	snp	C/G	1.73009e-05	0.00294111	missense	CHD4	GRCh38.p7	12:6602023	GGATTTGCTCTTCTT[C/G]TCTTTCTTAGGTCCA	1108
rs765576027	snp	A/G	3.31389e-05	0.00407042	missense	CHD4	GRCh38.p7	12:6600570	TTCGGAGTTTCTTGC[A/G]GCTGCGGCTACTACG	1108
rs765586646	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6580661	GCAGTAAGCCGAGAT[C/T]GCACCATTGCACTCC	1108
rs765623983	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6589253	ATCATTGTAATCAAG[A/G]TCCACTGACGAATAC	1108
rs765644907	in-del	-/CTTT	1.79181e-05	0.00299311	intron-variant	CHD4	GRCh38.p7	12:6600876	ATAGAAGGTCACATC[-/CTTT]CTATTAGACATGGCA	1108
rs765656187	snp	A/G			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608302	TGTCGCCCCACAGAT[A/G]GACATCTAATCTCTT	1108
rs765725275	snp	A/G	1.66471e-05	0.00288501	synonymous-codon	CHD4	GRCh38.p7	12:6602143	TGGCCCCTCCCCAGA[A/G]CTGTCCCCCAGCTGC	1108
rs765752721	snp	C/G	1.6531e-05	0.00287493	missense	CHD4	GRCh38.p7	12:6596014	CACTCACCTGTGATT[C/G]CAATAGCTCTGCTTG	1108
rs765765038	snp	C/T	1.77925e-05	0.0029826	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582311	AGAGAAAGAGTTAAA[C/T]AGGGATCATGCTGAC	1108
rs765768010	in-del	-/AAG	1.68367e-05	0.00290139	intron-variant	CHD4	GRCh38.p7	12:6595970	TCAAAAAAAAAAAAA[-/AAG]AAACAACTCTATGCC	1108
rs765787284	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6590187	TGGGCAACAGAGTGA[A/G]ACTCCATCCCGAAGA	1108
rs765831177	snp	C/T	0.000240993	0.0109744	intron-variant	CHD4	GRCh38.p7	12:6578691	CAGAAAATGGTGCCA[C/T]TGGCCCACTGACAAC	1108
rs765853114	in-del	-/T	1.70781e-05	0.00292212	intron-variant	CHD4	GRCh38.p7	12:6578186	GGAAGCAAACATCTG[-/T]TGAGAATTGAAAAAG	1108
rs765907058	snp	C/T	1.64803e-05	0.00287052	missense	CHD4	GRCh38.p7	12:6600261	GAGCCTTCTCCATGT[C/T]GGGATCCAGGCAGAC	1108
rs765946884	snp	A/C/T	3.35066e-05	0.00409297	synonymous-codon	CHD4	GRCh38.p7	12:6592413	CATAGGGCTCAGCTC[A/C/T]ACACGCACAATTAGT	1108
rs765949049	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6596487	AAACCCGTCTCTACT[-/A]AAAAAAAAAAAAAAA	1108
rs765960716	snp	C/T	1.65089e-05	0.00287301	splice-donor-variant	CHD4	GRCh38.p7	12:6578845	TTCTCCAAACACCCA[C/T]CTTTGTCTTCTACCA	1108
rs765961562	snp	C/T	3.77722e-05	0.00434565	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582094	AGGTGTGAGCCACTG[C/T]GCCTGGCCCCCTAGA	1108
rs765971201	in-del	-/AG			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569863	CTTGCTCAAGGTCAC[-/AG]AGCCATTAAGCGGCG	1108
rs766008460	snp	A/G			missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582261	TCACATAAATGCCGC[A/G]TGAAAAGAGAGACAT	1108
rs766029032	snp	A/G	9.88875e-05	0.00703093	missense	CHD4	GRCh38.p7	12:6601330	CGGATAGGCACCTCC[A/G]CAGGGGGAGGTGGTG	1108
rs766108188	snp	C/T	3.30196e-05	0.00406309	intron-variant	CHD4	GRCh38.p7	12:6602541	CAGGGAAAAGATCAA[C/T]AGCAAAAGGTTAGGC	1108
rs766220922	snp	A/T	6.62581e-05	0.0057554	intron-variant	CHD4	GRCh38.p7	12:6599730	CTACATAGAAAAGAC[A/T]ACACTTTCCCATTTT	1108
rs766225598	snp	C/T	3.34348e-05	0.00408855	intron-variant	CHD4	GRCh38.p7	12:6587340	CTCAATGCCAATTTT[C/T]AGACCAATTACCAAG	1108
rs766228217	snp	A/G	1.793e-05	0.00299411	intron-variant	CHD4	GRCh38.p7	12:6601101	AAGACCAAAGATGGG[A/G]AAAATAAAATCTTCT	1108
rs766239178	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6604791	GGAAAAAGTGGGTCA[C/T]GCTACAGCTCAGGAC	1108
rs766248477	snp	A/G	1.66507e-05	0.00288532	intron-variant	CHD4	GRCh38.p7	12:6592599	AAAAAAGTTATTGGA[A/G]AAGGAGAAAGGAAGA	1108
rs766261133	snp	C/T	1.66272e-05	0.00288328	intron-variant	CHD4	GRCh38.p7	12:6578947	GTTATTGAGACTATA[C/T]CTAAAGGAAGAACAT	1108
rs766309247	snp	G/T	1.70947e-05	0.00292354	missense	CHD4	GRCh38.p7	12:6606279	AAGATGTTACCTGGG[G/T]GGGGTGGGGGCAGGC	1108
rs766330469	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6580056	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	1108
rs766350426	in-del	-/AAAGA	1.66387e-05	0.00288428	intron-variant	CHD4	GRCh38.p7	12:6592614	GAAGGAGAAAGGAAG[-/AAAGA]AAAGTGATACAGGAA	1108
rs766382034	snp	A/T	0.000296976	0.0121819	intron-variant	CHD4	GRCh38.p7	12:6595314	CCCAACAAACTACAG[A/T]CCCTTCCACCCCCAC	1108
rs766383960	snp	A/G	1.64773e-05	0.00287026	intron-variant	CHD4	GRCh38.p7	12:6591647	TTTCCTTAGGTCACT[A/G]AGGGTTGTCTATGAC	1108
rs766397469	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6573763	GCACGGTGGCTCACA[C/T]CTGTAATCCCAGCAC	1108
rs766420024	snp	A/G	3.29826e-05	0.00406082	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581474	TTTGTCTCATCTTAA[A/G]TTGTCCTCTCGTGCC	1108
rs766427424	snp	A/G	1.64779e-05	0.00287031	synonymous-codon	CHD4	GRCh38.p7	12:6577890	GCGTGGGTCATTCTG[A/G]ATGTCTTGCCACCGG	1108
rs766446926	snp	C/G	1.65452e-05	0.00287616	missense	CHD4	GRCh38.p7	12:6578041	TACTTTATAATGCCG[C/G]CTAGCAGCCAGTAGT	1108
rs766474868	snp	G/T	3.30115e-05	0.00406259	intron-variant	CHD4	GRCh38.p7	12:6598115	CTTTGAGCGGAAAGA[G/T]AAAATCAGCCACCAA	1108
rs766504203	snp	A/T	1.64732e-05	0.0028699	missense	CHD4	GRCh38.p7	12:6599807	CATTCACCGTTGGGG[A/T]TCTCTGGAAGTGGGG	1108
rs766609805	snp	A/T	1.64727e-05	0.00286986	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581109	TTTTCCACTTTCTCC[A/T]CTCCCTCAGGGGGTT	1108
rs766615201	in-del	-/CT			intron-variant	CHD4	GRCh38.p7	12:6599657	GATGAAGGAGAATAC[-/CT]CTTTCTCAGGGCTGA	1108
rs766616340	snp	C/G/T	4.96014e-05	0.00497982	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582704	ACCATATCGCATAAT[C/G/T]GCATTAAGAAAGGCT	1108
rs766621258	in-del	-/G	9.96926e-05	0.00705949	intron-variant	CHD4	GRCh38.p7	12:6587691	GCCCCACACCAAAAC[-/G]TAAGTTCCTGACTAC	1108
rs766676555	snp	G/T	1.65743e-05	0.00287869	synonymous-codon	CHD4	GRCh38.p7	12:6600574	GAGTTTCTTGCGGCT[G/T]CGGCTACTACGGCTG	1108
rs766680001	snp	C/T	1.66366e-05	0.0028841	missense	CHD4	GRCh38.p7	12:6602151	CCCCAGAGCTGTCCC[C/T]CAGCTGCCGGCATAA	1108
rs766704254	snp	A/G			intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607153	GCCGGGCGCCCTGCA[A/G]GGCCAGGAAAGGAAG	1108
rs766721561	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6586427	ATAAATACATACATA[C/G]ATACATACACAAGGA	1108
rs766722943	snp	C/T	1.67674e-05	0.00289541	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582971	AATGAGTGACACAGG[C/T]AGGATATTAAACAAA	1108
rs766761589	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6594350	ATCCACAGTGTTCTT[C/G]AAGGTCAGAGACCAA	1108
rs766780672	snp	A/C/T	9.90776e-05	0.00703776	intron-variant	CHD4	GRCh38.p7	12:6598107	AGCTCCAGCTTTGAG[A/C/T]GGAAAGAGAAAATCA	1108
rs766785512	in-del	-/GGG	1.64814e-05	0.00287061	cds-indel	CHD4	GRCh38.p7	12:6601333	ATAGGCACCTCCACA[-/GGG]GGAGGTGGTGGTGCA	1108
rs766846637	snp	A/G	1.6504e-05	0.00287258	intron-variant	CHD4	GRCh38.p7	12:6601557	ATGCACAAGAGCAGA[A/G]GGAAAGGTTTAAGAA	1108
rs766852506	snp	C/T	1.75449e-05	0.00296178	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606381	GACGCCATCCCCTTC[C/T]GCTCCCGGCCAGGGA	1108
rs766869323	snp	A/T	1.64814e-05	0.00287061	missense	CHD4	GRCh38.p7	12:6597948	TTTATCCCATAGCGA[A/T]AGAAGCGTTCCTCCA	1108
rs766871406	snp	C/T	1.66114e-05	0.00288192	intron-variant	CHD4	GRCh38.p7	12:6600702	AATAAGGTTAGACGT[C/T]CAAGCCAAGGGGAAG	1108
rs766907162	snp	C/T	1.6795e-05	0.0028978	intron-variant	CHD4	GRCh38.p7	12:6578966	AAGGAAGAACATTCT[C/T]CTCTGTTGCACACTA	1108
rs766948802	snp	C/T	1.65277e-05	0.00287464	intron-variant	CHD4	GRCh38.p7	12:6592660	GAAGAATGAGAGGCA[C/T]AATTATGAGCCGATT	1108
rs766951652	in-del	-/CTT	0.0217	0.101878	cds-indel	CHD4	GRCh38.p7	12:6602041	TTTCTTAGGTCCAAG[-/CTT]CTTCTTCTTCTTCTT	1108
rs767006547	snp	C/G	1.64928e-05	0.00287161	synonymous-codon	CHD4	GRCh38.p7	12:6573081	CTGGCTACCTTTGTG[C/G]AGGACTGCATTGGCT	1108
rs767052844	in-del	-/GT			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607606	GCAGCGGGCGCGCGC[-/GT]GCGTCACCTGGGCAA	1108
rs767058556	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6597393	ATTGCTTGAGCCCAG[A/G]AGTTTGGGACAGCTA	1108
rs767071077	snp	A/G	3.32635e-05	0.00407807	intron-variant	CHD4	GRCh38.p7	12:6587361	AATTACCAAGCACAG[A/G]ATTGCCTTGGATTCA	1108
rs767089817	in-del	-/TCT	0.000149469	0.00864363	cds-indel	CHD4	GRCh38.p7	12:6578524	ATCACCTCTTTTTTC[-/TCT]TCTTCTTCTTCTTTC	1108
rs767126946	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6601943	CAGTACAAAGAAGAG[A/G]ATGGAGGTCCAGGCA	1108
rs767144895	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6592848	GAGAAAGGTGAAATC[C/T]AATGAAAACAGAGCT	1108
rs767174370	snp	C/T	1.7009e-05	0.0029162	missense	CHD4	GRCh38.p7	12:6606322	GTGCATCCATATCCT[C/T]CTCCTCACTGCCCGC	1108
rs767196536	snp	A/C	0.0021203	0.0324913	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582652	CTCGCAGGTCTCTTA[A/C]AAGCCACTGGGTAGT	1108
rs767199686	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6595680	GTAATCTCAGCTACT[C/T]GGGAGACTGAGGCAG	1108
rs767257985	snp	C/G	0.000214219	0.0103472	missense	CHD4	GRCh38.p7	12:6601337	GCACCTCCACAGGGG[C/G]AGGTGGTGGTGCAAC	1108
rs767352912	snp	C/T	1.64882e-05	0.00287121	intron-variant	CHD4	GRCh38.p7	12:6595326	CAGTCCCTTCCACCC[C/T]CACTCACATCAACTG	1108
rs767355615	in-del	-/GT	1.64993e-05	0.00287218	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570628	CTGGGACAAGAGAAA[-/GT]GAGGAAGGTCACTGC	1108
rs767368044	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	CHD4	GRCh38.p7	12:6599857	GTAGGAAGAAGGACA[A/G]GTATCACAGCAGAGC	1108
rs767371202	snp	C/T	0.000100627	0.0070925	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581673	GGACAGGTGCAGGAG[C/T]GTTGGGCTGCGTGTC	1108
rs767415730	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6595630	CCGTCTCTACTAAAA[A/C]TACAAAAATTAGCTG	1108
rs767432694	in-del	-/CTTT			intron-variant	CHD4	GRCh38.p7	12:6576605	CTGCCTCTCTGAGAA[-/CTTT]CTTTTCTTGTCTTTT	1108
rs767452064	snp	C/T	1.654e-05	0.00287571	intron-variant	CHD4	GRCh38.p7	12:6599735	TAGAAAAGACTACAC[C/T]TTCCCATTTTTTGCC	1108
rs767452369	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6594739	CCTCACTAGTCTTCA[C/T]GGATCCTCTTGGGGA	1108
rs767457617	snp	C/G	5.36006e-05	0.00517662	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582315	AAAGAGTTAAATAGG[C/G]ATCATGCTGACTCTT	1108
rs767493747	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6604884	AATGGGAGGCCAAGA[C/T]GTGGAACCCAGAATG	1108
rs767512181	in-del	-/AAC			intron-variant	CHD4	GRCh38.p7	12:6580238	CTCGAAAACAACAAC[-/AAC]AACAACAACAACAAC	1108
rs767535121	snp	C/T	3.32508e-05	0.00407729	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582834	ACCCCTCCTTAGAAT[C/T]GTATGGCACTTACTT	1108
rs767578728	snp	A/G	3.31411e-05	0.00407056	missense	CHD4	GRCh38.p7	12:6578063	GCCAGTAGTCATGCC[A/G]TCGATGCCAGATCTC	1108
rs767595540	snp	A/G	1.64732e-05	0.0028699	intron-variant	CHD4	GRCh38.p7	12:6591902	AGGGAGGAACAGGAG[A/G]TGGCACTACATACCA	1108
rs767604325	snp	G/T	1.7725e-05	0.00297694	intron-variant	CHD4	GRCh38.p7	12:6600920	AGCGATGGGCTGGGC[G/T]CTCACCGAGGATCTC	1108
rs767645057	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6573987	AGGATCGCGCCACTA[C/T]ACTCCAGCCTGAGTG	1108
rs767663720	in-del	-/G	0.000166309	0.00911739	intron-variant	CHD4	GRCh38.p7	12:6593257	AACTTGGTCACTACT[-/G]AGTCAGTTCCTCTGT	1108
rs767687389	snp	C/T	1.64792e-05	0.00287042	synonymous-codon	CHD4	GRCh38.p7	12:6595430	ACCCCTCATTAACTC[C/T]CTAAAGAAGAAAGAC	1108
rs767687805	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6605825	AAATAATCAGATAGA[C/G]TGTAACCAGCACTCC	1108
rs767731451	snp	A/C	1.69092e-05	0.00290763	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582981	ACAGGTAGGATATTA[A/C]ACAAAGCAACATTTA	1108
rs767775222	snp	A/G	5.13756e-05	0.00506805	intron-variant	CHD4	GRCh38.p7	12:6578188	GAAGCAAACATCTGT[A/G]AGAATTGAAAAAGCT	1108
rs767777981	snp	A/G	1.79544e-05	0.00299615	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606394	TCCGCTCCCGGCCAG[A/G]GAATTGGCCCAGCTG	1108
rs767798713	snp	C/T	4.97203e-05	0.00498575	intron-variant	CHD4	GRCh38.p7	12:6598207	CCCTACATCTCCAGA[C/T]TATCCTAAACTTACC	1108
rs767806005	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6573481	ATTTTTAAAACTCTT[C/T]ACCCTTTAGGTTCTC	1108
rs767838481	snp	C/T	1.6476e-05	0.00287014	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581270	GTCTTTAGTATGGCA[C/T]TCAGTCACCCCATCT	1108
rs767839551	snp	A/G	1.66868e-05	0.00288845	intron-variant	CHD4	GRCh38.p7	12:6600717	TCAAGCCAAGGGGAA[A/G]GACAGAGTGGCAGAG	1108
rs767847862	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6597770	CTCTGTCTCAAAAAC[-/A]AAAAAACAAACAAAA	1108
rs767916032	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6599174	TGGTGGTAAACACCT[A/G]TAATGCCAGCACTTA	1108
rs767926188	snp	A/G	1.64757e-05	0.00287012	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581185	TACACTTCAAAGGAA[A/G]AAAAAACAAAAACAA	1108
rs767930607	snp	C/G	1.64781e-05	0.00287033	synonymous-codon	CHD4	GRCh38.p7	12:6593554	CCACATTTCAAACTC[C/G]CGCTCCCAGTTGATG	1108
rs767972147	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6586533	AGTTCAAGACCATCC[C/T]GGGCAACATAGCAAG	1108
rs768036240	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6604393	GCTAGACAGATACTA[C/G]GGAATGAGACATTAG	1108
rs768062204	snp	C/T	0.00021553	0.0103787	intron-variant	CHD4	GRCh38.p7	12:6588260	GCCTTTCTAGCATAA[C/T]ATGTTACTTATTAAG	1108
rs768084377	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6580399	CATGGTTCACACAGG[C/G]ATCTGTAGTGCTTAA	1108
rs768088947	in-del	-/AAAT			intron-variant	CHD4	GRCh38.p7	12:6586402	TGAGATTCCATCTCA[-/AAAT]AAATAAATAAATACA	1108
rs768094866	snp	C/T	1.96427e-05	0.00313384	intron-variant	CHD4	GRCh38.p7	12:6573317	ACTGATAACTCACTT[C/T]ACTCACTTCTGACTG	1108
rs768105598	snp	A/G	1.66532e-05	0.00288554	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582959	AAGAAAAAGATGAAT[A/G]AGTGACACAGGTAGG	1108
rs768164957	snp	C/G/T	3.98941e-05	0.00446607	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606417	CCCAGCTGCTCCTGC[C/G/T]GGCGGCCTGAGGACC	1108
rs768174917	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6587125	TTAATAAAACACATA[G/T]GAGAAAATGACATTC	1108
rs768178662	snp	C/T	1.77134e-05	0.00297597	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583081	AAGCCACTGAGTAAT[C/T]GGACTGGTTGTCGGA	1108
rs768210099	in-del	-/CTCGGGCATT	1.65332e-05	0.00287512	frameshift-variant	CHD4	GRCh38.p7	12:6592005	CCTGGTTGCCACCAC[-/CTCGGGCATT]GAGTGCTTCAAAATT	1108
rs768247783	snp	A/G	1.6473e-05	0.00286988	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581161	CTGAGGCAGGGGCAG[A/G]GGCCTGTGTACACTT	1108
rs768250444	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6605433	ACAACAGTTCCCCCA[A/G]TCAGACAGGGTGGTT	1108
rs768271770	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6571879	GGCAGGAGAATCGCT[C/T]GAACCCGGGAGGCGG	1108
rs768321394	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6592628	GAAAGAAAAGTGATA[C/T]AGGAAATGGGCAACA	1108
rs768352551	in-del	-/AC	1.66946e-05	0.00288912	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582964	AAAGATGAATGAGTG[-/AC]ACAGGTAGGATATTA	1108
rs768354353	snp	C/T			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582411	AAGCCCACCACTGCA[C/T]GGGAAGGCTGATCTC	1108
rs768355084	snp	A/C/T	3.30149e-05	0.00406283	intron-variant	CHD4	GRCh38.p7	12:6601799	TCAAGTAAGTACCTG[A/C/T]CACCTAGTGCCCACA	1108
rs768366577	snp	A/G	1.64768e-05	0.00287021	synonymous-codon	CHD4	GRCh38.p7	12:6593503	GGCACGGCTGTCCTT[A/G]TCACCCACATAGGTT	1108
rs768385169	in-del	-/CCT			intron-variant	CHD4	GRCh38.p7	12:6596182	GCCAGAAAAGGCAAC[-/CCT]CCTCACTTCCTCTCA	1108
rs768399896	snp	A/T	3.38158e-05	0.00411178	intron-variant	CHD4	GRCh38.p7	12:6593636	GAGAAAAAAGAGGAG[A/T]GTCAGGACTGAGGGC	1108
rs768412958	snp	C/G	1.675e-05	0.00289391	intron-variant	CHD4	GRCh38.p7	12:6588450	CCAAAAACACCATTA[C/G]AAGTGTCTCCTAAAT	1108
rs768429912	snp	A/T	1.72844e-05	0.00293971	missense	CHD4	GRCh38.p7	12:6601970	GGCACCTTTGAATCA[A/T]CATCATCATCCTCCT	1108
rs768431642	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6600676	ATCCTCACTCTGGCA[A/G]GATGAAAAAGAATAA	1108
rs768438654	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6597043	GGAAGGAGGAGGTGA[A/G]CGGATCACAAGGTCA	1108
rs768443881	snp	A/G	1.64803e-05	0.00287052	missense	CHD4	GRCh38.p7	12:6573190	TTGAGGGCCATGGAA[A/G]GGTGAGAAGGGTCTT	1108
rs768500724	snp	C/T	1.68247e-05	0.00290035	intron-variant	CHD4	GRCh38.p7	12:6588001	TTTCCTGGTGCCACT[C/T]TTATCCTGACTTCCA	1108
rs768593929	snp	C/T	1.65097e-05	0.00287308	missense	CHD4	GRCh38.p7	12:6578909	CCACCTTCTCTACAT[C/T]AGCAGCACCTAGGGG	1108
rs768618221	snp	A/G			intron-variant, upstream-variant-2KB	CHD4	GRCh38.p7	12:6606479	GGGGGGAGAAACACA[A/G]AACAGTCAGTGACGC	1108
rs768624271	snp	A/G	3.30153e-05	0.00406283	synonymous-codon, intron-variant	CHD4	GRCh38.p7	12:6600394	AGTCACCTCCTCCTC[A/G]CCTGGGCAAGGAAGA	1108
rs768700809	snp	A/T	3.33778e-05	0.00408507	intron-variant	CHD4	GRCh38.p7	12:6595977	AAAAAAAAAAGAAAC[A/T]ACTCTATGCCTCACC	1108
rs768750436	snp	C/T	1.64914e-05	0.00287149	missense	CHD4	GRCh38.p7	12:6602495	CTGGGTCCTCTTCAT[C/T]TTCTACATATATTTG	1108
rs768750510	in-del	-/TCC	0.00444772	0.0469476	cds-indel	CHD4	GRCh38.p7	12:6601979	GAATCATCATCATCA[-/TCC]TCCTCCTCCTCCTCC	1108
rs768769285	snp	C/G	1.65241e-05	0.00287433	intron-variant	CHD4	GRCh38.p7	12:6570832	CTCCAGAATGGTTCT[C/G]CAGGAAGAGGTGGTG	1108
rs768776001	snp	C/T	1.69209e-05	0.00290864	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583359	TGTTTAATGATTTCC[C/T]GTTCTACCTCCTCTT	1108
rs768785035	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6577776	ATATATTCCTCCCCA[A/G]CCGCTCACCTTAAAC	1108
rs768787173	snp	C/T	1.76586e-05	0.00297136	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582595	TGCTCTAGATCAGTC[C/T]ACTCCAGCCCTCAAC	1108
rs768790200	snp	C/T	1.64795e-05	0.00287045	missense	CHD4	GRCh38.p7	12:6570897	GGTTCGGGTGCCCGG[C/T]TTGCCAGGCGGCTGA	1108
rs768873266	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6576321	GAGATCTTGCCACTG[A/C]ACTCCAGCCTGGCAA	1108
rs768891645	in-del	-/AA	1.65579e-05	0.00287727	intron-variant	CHD4	GRCh38.p7	12:6600681	CACTCTGGCAGGATG[-/AA]AAAGAATAAGGTTAG	1108
rs768893069	snp	C/T	1.65282e-05	0.00287469	intron-variant	CHD4	GRCh38.p7	12:6596146	GTCCACACTGCAAGT[C/T]CAGGAGAGAAAACCC	1108
rs769017025	snp	C/G	1.66879e-05	0.00288855	missense	CHD4	GRCh38.p7	12:6602121	CTTCCTCCTCCTCCA[C/G]AAACTCTGGCCCCTC	1108
rs769045295	snp	A/C/G	4.94404e-05	0.00497173	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581555	TTGCTGTGTGTCCTG[A/C/G]CAGACTACCCTGTTA	1108
rs769054925	snp	C/G	1.64898e-05	0.00287135	synonymous-codon	CHD4	GRCh38.p7	12:6601380	CACCATGCTCTCCAC[C/G]ACAGCTACCGCTGCT	1108
rs769083537	snp	A/G	3.34102e-05	0.00408705	intron-variant	CHD4	GRCh38.p7	12:6578155	GAGGAGGAATTTAGG[A/G]AAGGTTGGGGGTGGG	1108
rs769085265	snp	A/G			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569740	TTCCTAGAAACTAAC[A/G]TTAAGGTAGTGGTTA	1108
rs769110717	snp	A/G	3.63643e-05	0.0042639	intron-variant	CHD4	GRCh38.p7	12:6598472	TCATAACCATGGGAG[A/G]AGAAGGGACAGCCCA	1108
rs769135264	snp	C/T	1.64735e-05	0.00286993	missense	CHD4	GRCh38.p7	12:6587533	AGTGGATAACACTGC[C/T]ATCTTCTCCCTCTTT	1108
rs769181053	in-del	-/AAAA	0.000297713	0.012197	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581021	AACAAACAAACAAAC[-/AAAA]AAAATGTGGATACCT	1108
rs769183843	snp	A/T	4.9498e-05	0.00497459	intron-variant	CHD4	GRCh38.p7	12:6577957	ACAAAACAAGGAAAG[A/T]AAGAACCTCAAACTA	1108
rs769254265	snp	A/G	1.64765e-05	0.00287019	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581261	TACACATTTGTCTTT[A/G]GTATGGCATTCAGTC	1108
rs769258173	snp	C/G			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581960	GGTGCCCGCCACCAC[C/G]TGCAGCTAATTTTTG	1108
rs769301511	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6574622	GATGCTTCTCAAACA[G/T]GTACCTTCAGCACTG	1108
rs769305848	in-del	-/AG	8.24865e-05	0.00642156	intron-variant	CHD4	GRCh38.p7	12:6577955	AAACAAAACAAGGAA[-/AG]TAAGAACCTCAAACT	1108
rs769311269	snp	A/G	1.69807e-05	0.00291377	intron-variant	CHD4	GRCh38.p7	12:6593641	AAAAGAGGAGAGTCA[A/G]GACTGAGGGCCCCAG	1108
rs769323293	snp	A/G	1.64806e-05	0.00287054	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581413	AATAAAAGACAATCA[A/G]TTAGGAAGAAGGTAC	1108
rs769326957	snp	A/G	4.03023e-05	0.00448882	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606419	CAGCTGCTCCTGCCG[A/G]CGGCCTGAGGACCTC	1108
rs769346271	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6594280	TACATGTGTTTATCC[A/G]CTATCACATTTATCT	1108
rs769347541	in-del	-/TTTATATACT			intron-variant	CHD4	GRCh38.p7	12:6593835	CTCTCCCATTAAGTC[-/TTTATATACT]TTTTTTCTGAGACGG	1108
rs769359634	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583268	TTTGCCCAGATTTCG[A/G]GCTAGATCTTCTTGC	1108
rs769402080	snp	A/G	5.52797e-05	0.00525707	intron-variant	CHD4	GRCh38.p7	12:6573301	AGGAAACGGGAGTTC[A/G]ACTGATAACTCACTT	1108
rs769413202	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6595185	TCTGATATATAGAGA[C/T]GTGGAGAAGTGGGGA	1108
rs769433963	snp	C/T	1.65567e-05	0.00287716	intron-variant	CHD4	GRCh38.p7	12:6596159	GTCCAGGAGAGAAAA[C/T]CCTCAGAGCCAGAAA	1108
rs769476360	snp	C/T	3.29511e-05	0.00405887	missense	CHD4	GRCh38.p7	12:6577861	CCCTTGAAAGGCTCA[C/T]TGAGGATGGCATAGC	1108
rs769479484	snp	G/T	1.65113e-05	0.00287322	missense	CHD4	GRCh38.p7	12:6598328	GGGGAGGGCGTGTTG[G/T]GATCAGCATCTGGAG	1108
rs769503183	snp	C/T	1.69292e-05	0.00290935	intron-variant	CHD4	GRCh38.p7	12:6588467	AGTGTCTCCTAAATT[C/T]CAATTCATAAATGTA	1108
rs769524354	snp	A/G	1.6531e-05	0.00287493	intron-variant	CHD4	GRCh38.p7	12:6600410	CCTGGGCAAGGAAGA[A/G]GGAAAGCCCAGTTAT	1108
rs769545666	snp	C/T	5.24416e-05	0.00512036	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582605	CAGTCCACTCCAGCC[C/T]TCAACTCACTTGAAC	1108
rs769563825	in-del	-/A	0.000192886	0.00981865	intron-variant	CHD4	GRCh38.p7	12:6594430	ACAAAACACCCACAC[-/A]AAAAACTATCCACCC	1108
rs769566608	snp	A/G	1.66749e-05	0.00288741	intron-variant	CHD4	GRCh38.p7	12:6600524	ACAAATATACAGAAG[A/G]GAAACACACCTTTCT	1108
rs769599701	snp	A/G	3.39824e-05	0.0041219	synonymous-codon	CHD4	GRCh38.p7	12:6602074	GCCAGGAGTATAGTC[A/G]CTGCCCTCACTGTCT	1108
rs769632474	snp	C/G	1.75243e-05	0.00296004	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582291	TATGCCCTGTGTAAA[C/G]AAGTAGAGAAAGAGT	1108
rs769651089	snp	A/C/T	3.29757e-05	0.00406041	intron-variant, downstream-variant-500B, missense	CHD4, SCARNA11	GRCh38.p7	12:6581038	AAAAAATGTGGATAC[A/C/T]TTTACCTTTGGGCTC	1108
rs769675089	in-del	-/AGAA	6.65979e-05	0.00577014	intron-variant	CHD4	GRCh38.p7	12:6592073	CTACATGGGCAAGGT[-/AGAA]AGACAGGTTAGACTT	1108
rs769689377	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6573294	GGATAAGAGGAAACG[A/G]GAGTTCGACTGATAA	1108
rs769696217	snp	C/T	1.65195e-05	0.00287393	synonymous-codon	CHD4	GRCh38.p7	12:6601392	CACCACAGCTACCGC[C/T]GCTGCTGCCGCAGCT	1108
rs769701672	snp	A/C	1.64773e-05	0.00287026	missense	CHD4	GRCh38.p7	12:6570906	GCCCGGTTTGCCAGG[A/C]GGCTGAGAATGTTAC	1108
rs769744614	snp	G/T	1.65608e-05	0.00287752	intron-variant	CHD4	GRCh38.p7	12:6578927	CAGCACCTAGGGGAA[G/T]AAATGTTATTGAGAC	1108
rs769747716	snp	A/G	1.64792e-05	0.00287042	intron-variant	CHD4	GRCh38.p7	12:6573034	ATGCAGTCAGATCAG[A/G]GAGGCCGAATCGGCA	1108
rs769759908	snp	A/C	1.64866e-05	0.00287106	intron-variant	CHD4	GRCh38.p7	12:6597874	GGAGACTGCCCGTCT[A/C]CCGTGTGCTCAGCTG	1108
rs769769680	snp	A/G	1.66073e-05	0.00288156	missense	CHD4	GRCh38.p7	12:6588419	AACTGCTGAGCACCC[A/G]GTGCTAATAAAAGAA	1108
rs769907247	in-del	-/AT	3.54604e-05	0.00421057	frameshift-variant	CHD4	GRCh38.p7	12:6601980	ATCATCATCATCATC[-/AT]CTCCTCCTCCTCCTC	1108
rs769919523	snp	A/C	1.64783e-05	0.00287034	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581565	TCCTGCCAGACTACC[A/C]TGTTAGAACTGAGCA	1108
rs769937640	snp	C/T	1.64825e-05	0.00287071	missense	CHD4	GRCh38.p7	12:6601319	TCTTGGCCTTGCGGA[C/T]AGGCACCTCCACAGG	1108
rs769951286	snp	G/T	1.64882e-05	0.00287121	intron-variant	CHD4	GRCh38.p7	12:6587576	TATAAAAAATCAAGG[G/T]CCCACATCCCCAAAG	1108
rs769989060	snp	A/G	1.64773e-05	0.00287026	missense	CHD4	GRCh38.p7	12:6599781	CACTCACCGTACAAC[A/G]GGGACAGAGCCATTC	1108
rs770106384	snp	A/C	1.64738e-05	0.00286995	missense	CHD4	GRCh38.p7	12:6595398	TTCTTGAGCTTCTTG[A/C]CTGGTCGGCCTTCCT	1108
rs770143808	snp	C/G	1.64732e-05	0.0028699	missense	CHD4	GRCh38.p7	12:6591770	AGCAATAATTTCCCA[C/G]ATGCTCTGATTAGGG	1108
rs770152421	snp	A/G	1.64942e-05	0.00287173	intron-variant	CHD4	GRCh38.p7	12:6587676	CTTTAGAGAGGCCAA[A/G]CCCCACACCAAAACG	1108
rs770172669	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6578167	AGGGAAGGTTGGGGG[A/T]GGGGGGAAGCAAACA	1108
rs770181976	snp	A/T	1.64727e-05	0.00286986	missense	CHD4	GRCh38.p7	12:6599948	AGGTCTCCCCCAACC[A/T]CTTCCAGGATCTCCT	1108
rs770215085	in-del	-/AA	1.64866e-05	0.00287106	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581608	AAAATAGGCCAGGAC[-/AA]AAAGAGAGGGACAGA	1108
rs770219141	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6602955	AGGATCAGTTCAGGG[A/G]TCTCGGAAACCACAC	1108
rs770224021	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6602210	GAAGAGGGAGACAGA[C/T]ACACACATGCTACAC	1108
rs770231226	snp	C/T	1.65244e-05	0.00287436	synonymous-codon	CHD4	GRCh38.p7	12:6578485	CTCATCATTCAGGTC[C/T]TTGGGGGTCTCTCCA	1108
rs770236663	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6571517	TTCCATCTCAAGAAC[C/G]TGAATATGTTTAAAG	1108
rs770297208	snp	C/T	1.64732e-05	0.0028699	missense	CHD4	GRCh38.p7	12:6601667	CAAACTGGCTGAAGG[C/T]CTTGTAGTTGGTGAG	1108
rs770305324	snp	C/T			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569774	GTTAAAACCGTTCCA[C/T]GTACTTCACTGGTTT	1108
rs770414350	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6598670	AAAAATTAGCTGGGC[A/G]TGGTGGCATGCGCCT	1108
rs770416460	snp	C/T	1.6557e-05	0.00287719	intron-variant	CHD4	GRCh38.p7	12:6600679	CTCACTCTGGCAGGA[C/T]GAAAAAGAATAAGGT	1108
rs770418109	snp	C/T	1.67315e-05	0.00289231	missense	CHD4	GRCh38.p7	12:6602105	GAGCGCAGAGCCACC[C/T]CTTCCTCCTCCTCCA	1108
rs770418446	snp	C/T	1.64741e-05	0.00286998	missense	CHD4	GRCh38.p7	12:6602380	CACCCACTCACCTCC[C/T]TTTTTTGGCGCTTGC	1108
rs770448312	in-del	-/AAAC	0.000401912	0.0141702	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581005	CACTACACTGTCTCA[-/AAAC]AAACAAACAAACAAA	1108
rs770465075	snp	G/T	1.6498e-05	0.00287206	intron-variant	CHD4	GRCh38.p7	12:6577952	GAAAAACAAAACAAG[G/T]AAAGTAAGAACCTCA	1108
rs770495041	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6583794	GAGGATGACTATAAG[C/T]CTTTCTATTCTTCAT	1108
rs770516273	snp	A/T	1.74242e-05	0.00295157	intron-variant	CHD4	GRCh38.p7	12:6594691	GAGCTGGCAAGGAAC[A/T]CCCCTCCTCCCCTAA	1108
rs770534425	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6585089	AGACCACCAGAACCA[A/G]TGCCAACTGAAAGAA	1108
rs770570083	snp	C/T	3.31989e-05	0.00407411	missense	CHD4	GRCh38.p7	12:6600545	ACACCTTTCTTTTTC[C/T]TTTTAGTGGTTCGGA	1108
rs770593232	snp	A/G	1.66021e-05	0.0028811	intron-variant	CHD4	GRCh38.p7	12:6592837	TGAAGCAGATGGAGA[A/G]AGGTGAAATCCAATG	1108
rs770611625	snp	A/G	0.000131815	0.00811728	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581050	TACCTTTACCTTTGG[A/G]CTCTGTCTCCATAGG	1108
rs770630218	snp	C/T	3.31543e-05	0.00407137	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582648	TTGCCTCGCAGGTCT[C/T]TTACAAGCCACTGGG	1108
rs770674285	snp	A/G	3.30273e-05	0.00406356	synonymous-codon	CHD4	GRCh38.p7	12:6598022	CTCTTCATCACCACC[A/G]AAGTCCCCAGAAGGT	1108
rs770699429	snp	A/C/G	0.00011624	0.00762285	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582787	GAGAGGCAGCAGGTC[A/C/G]CATTCCACCAAAGAT	1108
rs770702848	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6605688	CCCCCATCACTTCCC[C/T]ACTCAAAACATTCCA	1108
rs770710887	snp	C/G	1.64735e-05	0.00286993	intron-variant	CHD4	GRCh38.p7	12:6591681	TCCCTAAAGCTCCCA[C/G]TCCACATGATACCTG	1108
rs770722140	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6588620	CTGTCTCTACTAAAA[A/G]TACAAAAATTAGCCA	1108
rs770762524	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6570819	GCAAAGTTACAAGCT[C/G]CAGAATGGTTCTGCA	1108
rs770766385	snp	A/T	1.65228e-05	0.00287422	missense	CHD4	GRCh38.p7	12:6600632	TTGATACTGGCATCA[A/T]CGAAGTCAGATTCCA	1108
rs770801247	snp	C/G	1.64746e-05	0.00287002	missense	CHD4	GRCh38.p7	12:6573124	GCCATTGACTCCTTG[C/G]ACAGGTGCTGATGAC	1108
rs770885235	snp	C/T	1.66054e-05	0.00288139	intron-variant	CHD4	GRCh38.p7	12:6587957	CTAAAGGCCTGGAGT[C/T]GAACAGGAAATAAAG	1108
rs770887217	snp	C/G			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582955	CAAGAAGAAAAAGAT[C/G]AATGAGTGACACAGG	1108
rs770890370	in-del	-/GGA	0.000163501	0.00904012	intron-variant	CHD4	GRCh38.p7	12:6598468	CAAATCATAACCATG[-/GGA]GGAGAAGGGACAGCC	1108
rs770916644	snp	C/T	1.65236e-05	0.00287429	missense	CHD4	GRCh38.p7	12:6593150	GGCAGGCCCAATCAA[C/T]AGAGCCCAAAATAGC	1108
rs770940592	snp	C/T	1.64779e-05	0.00287031	intron-variant	CHD4	GRCh38.p7	12:6601617	AACAGAAAGATTCTC[C/T]TCCCCCTTCCCCAAA	1108
rs770953034	snp	C/T	8.25743e-05	0.00642498	intron-variant	CHD4	GRCh38.p7	12:6599750	TTTCCCATTTTTTGC[C/T]CCGGCTGAGATCAGT	1108
rs770959943	snp	A/G	1.70235e-05	0.00291744	synonymous-codon	CHD4	GRCh38.p7	12:6606353	CGAGCAGGGGGACGG[A/G]GAGCCCAGGCCCGAC	1108
rs770996668	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6574717	ATACCAAAAGACTTG[C/T]CTAAAATTCGATATC	1108
rs771014996	in-del	-/CT	0.00027049	0.0116263	intron-variant	CHD4	GRCh38.p7	12:6594668	AAGGATGAAACAGAG[-/CT]AAGTCAAGAGCTGGC	1108
rs771049777	snp	C/T	1.70003e-05	0.00291545	missense	CHD4	GRCh38.p7	12:6606314	GTTCAAAAGTGCATC[C/T]ATATCCTCCTCCTCA	1108
rs771101225	snp	A/T	6.65779e-05	0.00576927	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581653	GGCAGACTTACCAGC[A/T]GGTGGGACAGGTGCA	1108
rs771132265	snp	A/C	1.64749e-05	0.00287005	missense	CHD4	GRCh38.p7	12:6595416	GGTCGGCCTTCCTCA[A/C]CCCTCATTAACTCCC	1108
rs771142773	snp	A/G	1.6473e-05	0.00286988	missense	CHD4	GRCh38.p7	12:6602461	AGCTTTGGAGTCTCT[A/G]TTTCTGACAAATCCT	1108
rs771161802	snp	A/G			intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581421	ACAATCAATTAGGAA[A/G]AAGGTACTAGATCAG	1108
rs771200646	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6599005	CCAGGATTTGCGTGC[C/T]ACCATCACTCCTATC	1108
rs771203360	snp	A/C			missense	CHD4	GRCh38.p7	12:6587471	TTCTGTGTCTTCAGT[A/C]TCATCCTGGTTACGG	1108
rs771213563	snp	G/T	3.30622e-05	0.00406571	missense	CHD4	GRCh38.p7	12:6578492	TTCAGGTCCTTGGGG[G/T]TCTCTCCATTCTGAA	1108
rs771238548	snp	A/G	1.66707e-05	0.00288705	intron-variant	CHD4	GRCh38.p7	12:6592081	GCAAGGTAGAAAGAC[A/G]GGTTAGACTTGAGAG	1108
rs771297359	snp	A/G	1.68303e-05	0.00290084	intron-variant	CHD4	GRCh38.p7	12:6578175	TTGGGGGTGGGGGGA[A/G]GCAAACATCTGTGAG	1108
rs771299383	snp	A/T	3.48068e-05	0.00417159	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581744	CCTGGCTGGGACATC[A/T]TCTTGTTTTCCTCCA	1108
rs771320675	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6594344	TCTATTATCCACAGT[A/G]TTCTTGAAGGTCAGA	1108
rs771328245	snp	C/G	1.64738e-05	0.00286995	intron-variant	CHD4	GRCh38.p7	12:6591896	CAACCCAGGGAGGAA[C/G]AGGAGATGGCACTAC	1108
rs771353473	snp	A/G	1.73213e-05	0.00294284	intron-variant, upstream-variant-2KB, missense	CHD4, SCARNA11	GRCh38.p7	12:6583123	GCCAATCTGGAGGGA[A/G]AGAGGGCAGATGAGC	1108
rs771364986	snp	C/T	7.13699e-05	0.00597326	intron-variant	CHD4	GRCh38.p7	12:6600907	GCACCCTCCCTAAAG[C/T]GATGGGCTGGGCTCT	1108
rs771386254	snp	C/G	1.64844e-05	0.00287087	intron-variant	CHD4	GRCh38.p7	12:6570712	GAGAAGGAGACCCGA[C/G]GAGTCAGAATTCCAG	1108
rs771507071	snp	A/G	1.656e-05	0.00287745	missense	CHD4	GRCh38.p7	12:6600554	TTTTTCTTTTTAGTG[A/G]TTCGGAGTTTCTTGC	1108
rs771518157	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6591014	TGTTGTCCCAGCTAC[G/T]TGGGAGGCTGAGGCA	1108
rs771520211	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6604235	AGCCAAGATCGCACA[C/T]TGCACTCCAACCTTG	1108
rs771541830	snp	A/G	1.65217e-05	0.00287412	missense	CHD4	GRCh38.p7	12:6600641	GCATCATCGAAGTCA[A/G]ATTCCACATCTAAGT	1108
rs771560867	snp	A/G	1.73003e-05	0.00294106	missense	CHD4	GRCh38.p7	12:6601042	CCTTGGGCTTCCTCC[A/G]AGCATTGGGACCTAA	1108
rs771561972	snp	A/G	1.64727e-05	0.00286986	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581148	ACCTTTTCATCCTCT[A/G]AGGCAGGGGCAGGGG	1108
rs771572189	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6597618	AAAAATACAAAAAAT[C/T]AGCTGGGCATGGTGG	1108
rs771610697	in-del	-/A	1.80794e-05	0.00300656	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581821	TCCTGAACCTGTAGC[-/A]AATGGGACAAGAAGT	1108
rs771625055	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6571657	ATGGAGAAACCCCAT[A/C]TCTACTAAAAATACA	1108
rs771663494	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6585172	ATTTCATACCCCTCT[A/G]TATCATTTAGGAGAG	1108
rs771683570	snp	A/G	3.29506e-05	0.00405884	intron-variant	CHD4	GRCh38.p7	12:6591872	AAGAAAGCCCACATG[A/G]AGAAGACCCAACCCA	1108
rs771698270	snp	G/T	3.30382e-05	0.00406423	synonymous-codon	CHD4	GRCh38.p7	12:6598070	CTTCCGCTGATAGTT[G/T]CGGAACATCACCTGA	1108
rs771714916	snp	A/G			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569977	CCAGTTACTCAGTGG[A/G]GTATCAGGACACCAC	1108
rs771725476	snp	A/G	3.29565e-05	0.00405921	intron-variant	CHD4	GRCh38.p7	12:6587701	AAAACGTAAGTTCCT[A/G]ACTACCTCACCTCCA	1108
rs771735196	in-del	-/A	0.00018521	0.00962137	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581183	TGTACACTTCAAAGG[-/A]AAAAAAAACAAAAAC	1108
rs771751276	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6603005	AGTCATCACTGCTCA[A/G]ATTAACCAGAACCTC	1108
rs771751856	snp	C/T	1.64781e-05	0.00287033	missense	CHD4	GRCh38.p7	12:6573176	CAGCAAAGCGGGTGT[C/T]GAGGGCCATGGAAGG	1108
rs771773391	snp	C/T	1.64732e-05	0.0028699	intron-variant	CHD4	GRCh38.p7	12:6591688	AGCTCCCAGTCCACA[C/T]GATACCTGGGAAAAG	1108
rs771774996	snp	A/T			intron-variant	CHD4	GRCh38.p7	12:6598997	GACATCGTCCAGGAT[A/T]TGCGTGCCACCATCA	1108
rs771783234	snp	C/T	1.64741e-05	0.00286998	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581062	TGGGCTCTGTCTCCA[C/T]AGGTTCCTCTGTTCT	1108
rs771791136	snp	C/G	1.71678e-05	0.00292978	synonymous-codon	CHD4	GRCh38.p7	12:6606365	CGGGGAGCCCAGGCC[C/G]GACGCCATCCCCTTC	1108
rs771802933	snp	C/T	1.64779e-05	0.00287031	synonymous-codon	CHD4	GRCh38.p7	12:6593476	AAAGGAGAACTCATT[C/T]TCTCGGATGATGGCA	1108
rs771875799	snp	A/G	1.65924e-05	0.00288027	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582931	TACGACTGGGCCTAC[A/G]GGGAGCTGCAAGAAG	1108
rs771883614	snp	C/G			upstream-variant-2KB	CHD4	GRCh38.p7	12:6609417	CCCTACTTACTAGGG[C/G]ATTTTTCTTGGAAAG	1108
rs771894555	snp	A/G	1.6574e-05	0.00287867	synonymous-codon	CHD4	GRCh38.p7	12:6593183	TGTCAATGGTGATCA[A/G]TTCATAGGATGTCAG	1108
rs771901202	in-del	-/CAGA	5.00229e-05	0.0050009	intron-variant	CHD4	GRCh38.p7	12:6600206	AGGGGCCACAATGGC[-/CAGA]CACTCACGCAGTGTG	1108
rs771933231	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6586467	TGGTGGCTAACACCT[A/G]TAATTCCAGCACTTT	1108
rs771937303	snp	C/T	1.64757e-05	0.00287012	intron-variant	CHD4	GRCh38.p7	12:6601628	TCTCCTCCCCCTTCC[C/T]CAAACCCCTTCTGTT	1108
rs772007453	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6595969	CTCAAAAAAAAAAAA[A/G]AAGAAACAACTCTAT	1108
rs772022193	in-del	-/T			intron-variant	CHD4	GRCh38.p7	12:6579971	GAGGCAGGAGAATGG[-/T]TGTGAACCCGGGAGG	1108
rs772022640	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6605936	CCCCCCTCCACCACC[A/C]CCACCACAAGCCTCC	1108
rs772026127	snp	A/G	1.74595e-05	0.00295456	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582146	GCTCACCTTCTTGCG[A/G]ATCAAAGACATAACA	1108
rs772059884	in-del	-/C			intron-variant	CHD4	GRCh38.p7	12:6580247	CAACAACAACAACAA[-/C]AACAACAACAAATAA	1108
rs772102293	in-del	-/AAG	5.19656e-05	0.00509707	intron-variant	CHD4	GRCh38.p7	12:6601935	AAGTTTAACAGTACA[-/AAG]AAGAGGATGGAGGTC	1108
rs772109809	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6589925	CTATATTGACCAGGC[A/C]CAGTGGCTCACACCT	1108
rs772112037	snp	C/T	1.66023e-05	0.00288113	synonymous-codon	CHD4	GRCh38.p7	12:6588418	GAACTGCTGAGCACC[C/T]GGTGCTAATAAAAGA	1108
rs772135339	snp	A/G	3.29723e-05	0.00406018	intron-variant	CHD4	GRCh38.p7	12:6601778	GCTCCTGCAGAAAGA[A/G]CAAAGTCAAGTAAGT	1108
rs772169095	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6596527	GCATCAGGCCGGGCG[C/T]GGTGGCTCACGCCTA	1108
rs772239869	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	CHD4	GRCh38.p7	12:6599866	AGGACAGGTATCACA[A/G]CAGAGCAGTTCCCCA	1108
rs772248307	snp	C/T	4.9436e-05	0.00497148	synonymous-codon	CHD4	GRCh38.p7	12:6602478	TTCTGACAAATCCTC[C/T]TCTGGGTCCTCTTCA	1108
rs772259594	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6574840	TTCTGTACCTCAAAT[C/T]CAGTAAGTCAGGAGT	1108
rs772336282	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	CHD4	GRCh38.p7	12:6602397	TTTTTGGCGCTTGCT[C/T]TTAGGGATTTTAGGG	1108
rs772395098	snp	A/G	1.64765e-05	0.00287019	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583292	TTCTTGCTGCTGCTC[A/G]TAATGGTGCCGCAGC	1108
rs772412478	in-del	-/G	1.78998e-05	0.00299159	intron-variant	CHD4	GRCh38.p7	12:6573292	GGGATAAGAGGAAAC[-/G]GGGAGTTCGACTGAT	1108
rs772445792	snp	A/G	1.74017e-05	0.00294967	intron-variant	CHD4	GRCh38.p7	12:6606232	ACTCGGGAGAGCCCC[A/G]GATGTCTCCTTCCCG	1108
rs772455190	snp	C/G	0.000138182	0.00831095	intron-variant	CHD4	GRCh38.p7	12:6578722	TAAATGTGGGGACAG[C/G]TACAGTCTTTTATCT	1108
rs772457322	snp	G/T	1.65007e-05	0.00287229	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570630	GGGACAAGAGAAAGT[G/T]AGGAAGGTCACTGCT	1108
rs772502595	snp	C/T	1.64814e-05	0.00287061	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581540	TAAACTGAGAGGGAA[C/T]TGCTGTGTGTCCTGC	1108
rs772512300	snp	A/G	1.74964e-05	0.00295769	intron-variant	CHD4	GRCh38.p7	12:6601057	GAGCATTGGGACCTA[A/G]AATCAGGATATATCC	1108
rs772550482	snp	G/T	1.64754e-05	0.00287009	missense	CHD4	GRCh38.p7	12:6577842	ATTGCCACGGTTCAT[G/T]TCACCCTTGAAAGGC	1108
rs772555151	snp	C/T	1.64904e-05	0.00287139	synonymous-codon	CHD4	GRCh38.p7	12:6592503	CCCCAGCATGTCATG[C/T]AGTTTTTTTATCTGG	1108
rs772592474	snp	A/G	4.94417e-05	0.00497176	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581427	AATTAGGAAGAAGGT[A/G]CTAGATCAGAGAGAA	1108
rs772623855	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6583626	TATTATCACAGGTAA[A/G]GATGAAGAGACAGAA	1108
rs772656983	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6594203	ATTCCCCTAGAACTG[A/G]TACTCTATGGATCCA	1108
rs772693847	snp	A/G	1.72546e-05	0.00293718	intron-variant	CHD4	GRCh38.p7	12:6593656	GGACTGAGGGCCCCA[A/G]CACACTGCAACCCCA	1108
rs772714006	snp	A/C	1.7582e-05	0.00296491	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582296	CCTGTGTAAAGAAGT[A/C]GAGAAAGAGTTAAAT	1108
rs772799886	snp	C/G	1.68664e-05	0.00290395	intron-variant	CHD4	GRCh38.p7	12:6591416	AAGTTACAGTCCAAA[C/G]ATATAAGCAAATGAG	1108
rs772823276	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6572083	GTGAGCCGAGATCAC[G/T]CCATTGCACCCCAGC	1108
rs772857309	snp	C/G	1.70258e-05	0.00291764	intron-variant	CHD4	GRCh38.p7	12:6593644	AGAGGAGAGTCAGGA[C/G]TGAGGGCCCCAGCAC	1108
rs772879615	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6573580	CACCTTCTAGAAATA[C/T]ATCCTGATATTTTTC	1108
rs772882427	snp	C/T	1.6554e-05	0.00287693	intron-variant	CHD4	GRCh38.p7	12:6600417	AAGGAAGAGGGAAAG[C/T]CCAGTTATTGGAAAA	1108
rs772890826	snp	A/G	1.6477e-05	0.00287024	synonymous-codon	CHD4	GRCh38.p7	12:6591551	ACCTTCATGTTCCAA[A/G]AAATCCTCTAGCAGG	1108
rs772975636	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6594293	CCACTATCACATTTA[C/T]CTACTATCTACTAAA	1108
rs772981042	snp	A/C	4.9445e-05	0.00497193	synonymous-codon	CHD4	GRCh38.p7	12:6601323	GGCCTTGCGGATAGG[A/C]ACCTCCACAGGGGGA	1108
rs772996422	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6605529	CACCTACACAGACAC[C/T]TCACACTGCCAGCCT	1108
rs773003594	snp	C/T	1.64792e-05	0.00287042	synonymous-codon	CHD4	GRCh38.p7	12:6592770	TAATGGTGTCCCAGT[C/T]AGCAACAGCTTGTGC	1108
rs773022790	snp	C/T	1.6543e-05	0.00287597	intron-variant	CHD4	GRCh38.p7	12:6578829	CTGAACCACAATCAA[C/T]TTCTCCAAACACCCA	1108
rs773073170	snp	A/G	1.71779e-05	0.00293064	intron-variant	CHD4	GRCh38.p7	12:6606261	CGCCATGGGCCCTTG[A/G]GGAAGATGTTACCTG	1108
rs773075599	snp	C/T	1.65638e-05	0.00287778	intron-variant	CHD4	GRCh38.p7	12:6596162	CAGGAGAGAAAACCC[C/T]CAGAGCCAGAAAAGG	1108
rs773089748	snp	C/T	3.47144e-05	0.00416605	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582612	CTCCAGCCCTCAACT[C/T]ACTTGAACTCTTTCT	1108
rs773093618	snp	C/T	6.59424e-05	0.00574168	intron-variant	CHD4	GRCh38.p7	12:6597876	AGACTGCCCGTCTCC[C/T]GTGTGCTCAGCTGGT	1108
rs773125129	snp	A/G	1.64765e-05	0.00287019	missense	CHD4	GRCh38.p7	12:6570907	CCCGGTTTGCCAGGC[A/G]GCTGAGAATGTTACG	1108
rs773125431	in-del	-/AA	1.66358e-05	0.00288402	intron-variant	CHD4	GRCh38.p7	12:6592584	TCAGAAAGAAAAAGG[-/AA]AAAAGTTATTGGAGA	1108
rs773139218	snp	C/T			utr-variant-3-prime	CHD4	GRCh38.p7	12:6570475	TGGCGCCAGCGCTAC[C/T]GCTGCATGTCTCTTC	1108
rs773143964	in-del	-/AC	1.6832e-05	0.00290099	intron-variant	CHD4	GRCh38.p7	12:6594663	TGGCTGAAGGATGAA[-/AC]AGAGAAGTCAAGAGC	1108
rs773161450	snp	C/T	3.39986e-05	0.00412288	missense	CHD4	GRCh38.p7	12:6606310	TGTTGTTCAAAAGTG[C/T]ATCCATATCCTCCTC	1108
rs773231922	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6584046	TACAATCGGCCCTCT[G/T]TATCCACGGGTTCCG	1108
rs773241996	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6603150	TTCTCCCTAGGGGCC[C/G]GAATCAGCCCAGCTG	1108
rs773242698	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6579511	ATTGTTTGAACCCAG[C/G]AGGTGGAGGTTGCAG	1108
rs773248387	snp	C/T	1.6722e-05	0.00289149	intron-variant	CHD4	GRCh38.p7	12:6587333	CCTTGGTCTCAATGC[C/T]AATTTTCAGACCAAT	1108
rs773272625	snp	C/T	1.64773e-05	0.00287026	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581569	GCCAGACTACCCTGT[C/T]AGAACTGAGCACAGG	1108
rs773326114	snp	A/G	1.64795e-05	0.00287045	intron-variant	CHD4	GRCh38.p7	12:6573035	TGCAGTCAGATCAGG[A/G]AGGCCGAATCGGCAG	1108
rs773353159	snp	C/T	0.00011653	0.00763225	intron-variant	CHD4	GRCh38.p7	12:6592594	AAAGGAAAAAAGTTA[C/T]TGGAGAAGGAGAAAG	1108
rs773397682	snp	C/T	8.27191e-05	0.00643061	intron-variant	CHD4	GRCh38.p7	12:6595291	TGCAGCAAAGATACA[C/T]TGTCCTACCCAACAA	1108
rs773444998	snp	A/G	8.24477e-05	0.00642005	intron-variant	CHD4	GRCh38.p7	12:6587582	AAATCAAGGGCCCAC[A/G]TCCCCAAAGTCAGTT	1108
rs773461453	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6580154	ATCGCTTGAACCCAG[A/G]AGGCGGGAGTTGCAG	1108
rs773468760	snp	C/T	1.65449e-05	0.00287614	missense	CHD4	GRCh38.p7	12:6578039	GATACTTTATAATGC[C/T]GGCTAGCAGCCAGTA	1108
rs773476275	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	CHD4	GRCh38.p7	12:6591787	TGCTCTGATTAGGGC[A/G]CTGCCATCATACATG	1108
rs773486233	snp	A/G	1.67764e-05	0.00289619	intron-variant	CHD4	GRCh38.p7	12:6578168	GGGAAGGTTGGGGGT[A/G]GGGGGAAGCAAACAT	1108
rs773553565	snp	C/G	3.30972e-05	0.00406786	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581638	GAAAATGATAGGACA[C/G]GCAGACTTACCAGCA	1108
rs773573339	snp	A/G	1.64741e-05	0.00286998	missense	CHD4	GRCh38.p7	12:6595402	TGAGCTTCTTGCCTG[A/G]TCGGCCTTCCTCACC	1108
rs773599172	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6590824	GTGAGACCCTATCTC[A/G]AATAAACAAAACAAA	1108
rs773654195	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6590219	GAAAAAAAATCTGTA[C/T]CATATAAGAAAATAA	1108
rs773655988	snp	C/T	1.66208e-05	0.00288273	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582816	ATGCAATATCTGACA[C/T]TCACCCCTCCTTAGA	1108
rs773668561	snp	A/C/T	3.31204e-05	0.00406931	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582650	GCCTCGCAGGTCTCT[A/C/T]ACAAGCCACTGGGTA	1108
rs773687092	in-del	-/CTT	5.19679e-05	0.00509718	cds-indel	CHD4	GRCh38.p7	12:6601998	CTCCTCCTCCTCCTC[-/CTT]CTTCCGCTTGGATTT	1108
rs773696559	snp	A/C	1.65652e-05	0.0028779	intron-variant	CHD4	GRCh38.p7	12:6602212	AGAGGGAGACAGACA[A/C]ACACATGCTACACAC	1108
rs773707679	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6591082	GAGCCAAGATCGTGC[C/G]GCTGCACTCCAGCCT	1108
rs773723495	snp	C/T	3.3451e-05	0.00408954	synonymous-codon	CHD4	GRCh38.p7	12:6602107	GCGCAGAGCCACCTC[C/T]TCCTCCTCCTCCACA	1108
rs773742613	snp	A/G	1.66924e-05	0.00288893	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582964	AAAGATGAATGAGTG[A/G]CACAGGTAGGATATT	1108
rs773756010	snp	A/G			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569820	TGAGGTATACATGAG[A/G]TATCTGCATCCCACC	1108
rs773804732	snp	A/G	1.64901e-05	0.00287137	intron-variant	CHD4	GRCh38.p7	12:6600894	TCTATTAGACATGGC[A/G]CCCTCCCTAAAGCGA	1108
rs773836717	in-del	-/T			intron-variant	CHD4	GRCh38.p7	12:6598807	GAGCAAGACTCCATC[-/T]CAAAAAAATAAAAAA	1108
rs773838913	snp	C/T	1.67823e-05	0.0028967	intron-variant	CHD4	GRCh38.p7	12:6600446	AAAAACTACCTCCCC[C/T]CACCCCCCGACCCCT	1108
rs773882148	in-del	-/CAAA			intron-variant	CHD4	GRCh38.p7	12:6577538	ATCTGCAGTGTTCCC[-/CAAA]CAAACCCCTCTGCAC	1108
rs773894753	snp	C/T	4.94181e-05	0.00497057	missense	CHD4	GRCh38.p7	12:6602383	CCACTCACCTCCTTT[C/T]TTTGGCGCTTGCTCT	1108
rs773894821	snp	A/T	1.65927e-05	0.00288029	intron-variant	CHD4	GRCh38.p7	12:6600695	GAAAAAGAATAAGGT[A/T]AGACGTTCAAGCCAA	1108
rs773897725	in-del	-/CAC	3.31307e-05	0.00406992	cds-indel	CHD4	GRCh38.p7	12:6578512	TCCATTCTGAAGCAT[-/CAC]CTCTTTTTTCTCTTC	1108
rs773900331	snp	A/G	1.64966e-05	0.00287194	intron-variant	CHD4	GRCh38.p7	12:6577953	AAAAACAAAACAAGG[A/G]AAGTAAGAACCTCAA	1108
rs773916967	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6602981	CACACCCTTCTCTAA[C/T]CACTTTGAAGTCATC	1108
rs773936987	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6583801	ACTATAAGCCTTTCT[A/G]TTCTTCATAAACTTC	1108
rs773945240	snp	C/G	1.64814e-05	0.00287061	intron-variant	CHD4	GRCh38.p7	12:6597890	CCGTGTGCTCAGCTG[C/G]TACCTGTGGTTGAGG	1108
rs773996522	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6597338	AGGCGCAGTAGCTCA[C/T]GCCTGTAATCCTAAC	1108
rs773999266	snp	A/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6607843	ACATCCTTTGCCAAC[A/T]TCTTCTTCACTCTTG	1108
rs774036270	snp	A/G/T	8.28529e-05	0.0064359	missense	CHD4	GRCh38.p7	12:6600551	TTCTTTTTCTTTTTA[A/G/T]TGGTTCGGAGTTTCT	1108
rs774057652	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6598733	AGAATCACTTGAACC[C/T]GGGAGGCAGAGCTTG	1108
rs774088519	snp	A/G	3.41548e-05	0.00413234	synonymous-codon	CHD4	GRCh38.p7	12:6606281	GATGTTACCTGGGTG[A/G]GGTGGGGGCAGGCTG	1108
rs774111840	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6576365	TGTCTCAGGAAAAAA[A/C]AAAACAAAACAGGGT	1108
rs774117810	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	CHD4	GRCh38.p7	12:6599830	AAGTGGGGGATTCAG[A/G]CAGTGGATGTGGTAG	1108
rs774138764	snp	A/C	3.30344e-05	0.004064	missense	CHD4	GRCh38.p7	12:6598030	CACCACCAAAGTCCC[A/C]AGAAGGTGGCTCATC	1108
rs774203277	snp	C/G/T	3.32919e-05	0.00407983	intron-variant	CHD4	GRCh38.p7	12:6592847	GGAGAAAGGTGAAAT[C/G/T]CAATGAAAACAGAGC	1108
rs774214001	snp	C/T	1.65397e-05	0.00287569	missense	CHD4	GRCh38.p7	12:6593162	CAATAGAGCCCAAAA[C/T]AGCCATGTCAATGGT	1108
rs774243580	snp	A/C	1.6477e-05	0.00287024	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581051	ACCTTTACCTTTGGG[A/C]TCTGTCTCCATAGGT	1108
rs774282876	snp	C/T	1.70107e-05	0.00291634	missense	CHD4	GRCh38.p7	12:6606318	AAAAGTGCATCCATA[C/T]CCTCCTCCTCACTGC	1108
rs774312344	snp	C/G	8.24885e-05	0.00642164	intron-variant	CHD4	GRCh38.p7	12:6595316	CAACAAACTACAGTC[C/G]CTTCCACCCCCACTC	1108
rs774336964	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	CHD4	GRCh38.p7	12:6607348	TCGGTGTCACTCCCG[C/T]TCCGGCTCCTCCTCG	1108
rs774352289	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6579683	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	1108
rs774371323	snp	C/T	1.6473e-05	0.00286988	missense	CHD4	GRCh38.p7	12:6602392	TCCTTTTTTTGGCGC[C/T]TGCTCTTAGGGATTT	1108
rs774372997	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6574727	ACTTGTCTAAAATTC[A/G]ATATCATTCTTTTCT	1108
rs774407789	in-del	-/T			intron-variant	CHD4	GRCh38.p7	12:6572872	CCAGGAGTCCATCTC[-/T]TTTAAAAAAAAAAAA	1108
rs774415562	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6605739	AAGCACTCCAGATCC[C/T]GCTGAGGAGCGCGAT	1108
rs774471386	in-del	-/T			intron-variant	CHD4	GRCh38.p7	12:6590966	CATCTCTACTAAAAA[-/T]ACAAAAATTAGCTGG	1108
rs774481284	snp	C/T	3.29527e-05	0.00405898	missense	CHD4	GRCh38.p7	12:6601456	TTATTGGTACTGAAC[C/T]CCCGCCATTTTGCAC	1108
rs774499023	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6599048	CCAGTAGTTAGACTT[C/T]AACAATAAGCCAGAA	1108
rs774512174	snp	A/G	1.69361e-05	0.00290994	intron-variant	CHD4	GRCh38.p7	12:6578180	GGTGGGGGGAAGCAA[A/G]CATCTGTGAGAATTG	1108
rs774516204	snp	C/T	3.4929e-05	0.00417891	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581751	GGGACATCTTCTTGT[C/T]TTCCTCCACCTCAGC	1108
rs774529722	in-del	-/CT			intron-variant	CHD4	GRCh38.p7	12:6597756	GGGCACAGAGTGAGA[-/CT]CTGTCTCAAAAACAA	1108
rs774536825	snp	A/G	9.88403e-05	0.00702925	intron-variant	CHD4	GRCh38.p7	12:6591898	ACCCAGGGAGGAACA[A/G]GAGATGGCACTACAT	1108
rs774585525	in-del	-/AATGAA	0.000832334	0.0203832	intron-variant	CHD4	GRCh38.p7	12:6592849	AGAAAGGTGAAATCC[-/AATGAA]AACAGAGCTCTAGCA	1108
rs774602116	snp	A/G	1.66846e-05	0.00288826	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581663	CCAGCAGGTGGGACA[A/G]GTGCAGGAGTGTTGG	1108
rs774682821	snp	A/G	8.28041e-05	0.00643391	intron-variant	CHD4	GRCh38.p7	12:6602215	GGGAGACAGACACAC[A/G]CATGCTACACACATG	1108
rs774702950	snp	C/T	1.6476e-05	0.00287014	missense	CHD4	GRCh38.p7	12:6595419	CGGCCTTCCTCACCC[C/T]TCATTAACTCCCTAA	1108
rs774714132	snp	A/C	1.65858e-05	0.00287969	missense	CHD4	GRCh38.p7	12:6578515	ATTCTGAAGCATCAC[A/C]TCTTTTTTCTCTTCT	1108
rs774731111	snp	C/T	1.66774e-05	0.00288763	intron-variant	CHD4	GRCh38.p7	12:6592085	GGTAGAAAGACAGGT[C/T]AGACTTGAGAGCCTT	1108
rs774752711	in-del	-/AA			intron-variant	CHD4	GRCh38.p7	12:6577426	CTGCCTCAAAAAAAA[-/AA]AAAAAAAAAAAACAA	1108
rs774774023	snp	C/T	2.0425e-05	0.00319564	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606424	GCTCCTGCCGGCGGC[C/T]TGAGGACCTCTACAC	1108
rs774777050	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6578193	AAACATCTGTGAGAA[C/T]TGAAAAAGCTACTTA	1108
rs774873519	snp	A/C	1.65252e-05	0.00287443	missense	CHD4	GRCh38.p7	12:6600657	ATTCCACATCTAAGT[A/C]ATCATCCTCACTCTG	1108
rs774951254	snp	C/T	0.000132109	0.00812632	missense	CHD4	GRCh38.p7	12:6598331	GAGGGCGTGTTGGGA[C/T]CAGCATCTGGAGGCC	1108
rs774960116	in-del	-/A	7.2037e-05	0.00600111	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582330	ATCATGCTGACTCTT[-/A]AGATTCTTTTCCATC	1108
rs775014585	in-del	-/AA	0.0117732	0.0758154	intron-variant	CHD4	GRCh38.p7	12:6595957	GCAAGACTCCATCTC[-/AA]AAAAAAAAAAAAAGA	1108
rs775024529	snp	C/T	1.70304e-05	0.00291803	missense	CHD4	GRCh38.p7	12:6606327	TCCATATCCTCCTCC[C/T]CACTGCCCGCCGAGC	1108
rs775064390	snp	A/G			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6570049	CGCACACACTCATCC[A/G]CCTGCACCTACACCC	1108
rs775071344	snp	A/G	1.65206e-05	0.00287403	synonymous-codon	CHD4	GRCh38.p7	12:6598073	CCGCTGATAGTTTCG[A/G]AACATCACCTGACAG	1108
rs775084830	in-del	-/AAAAAC	1.64753e-05	0.00287008	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581187	CACTTCAAAGGAAAA[-/AAAAAC]AAAAACAAAACAGAT	1108
rs775086346	snp	C/T	1.64743e-05	0.00287	synonymous-codon, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581066	CTCTGTCTCCATAGG[C/T]TCCTCTGTTCTCTCC	1108
rs775086431	snp	A/G	3.31829e-05	0.00407313	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582936	CTGGGCCTACGGGGA[A/G]CTGCAAGAAGAAAAA	1108
rs775097214	in-del	-/T			intron-variant	CHD4	GRCh38.p7	12:6594396	TCTCTCTACTCAGTG[-/T]TAAGTTAAGGCTTCA	1108
rs775099272	snp	C/G	1.66026e-05	0.00288115	missense	CHD4	GRCh38.p7	12:6593216	GCACATGGAATTTCA[C/G]AGATGCCTCTTTCTG	1108
rs775122590	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6597001	TAGGCCGAGTGCGGC[A/G]GCTCACGCCTGTAAT	1108
rs775138409	snp	C/T	1.72943e-05	0.00294055	missense	CHD4	GRCh38.p7	12:6606370	AGCCCAGGCCCGACG[C/T]CATCCCCTTCCGCTC	1108
rs775146780	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6586071	CACCACTGAACTCCA[A/G]CCTGGGCAACAGAGC	1108
rs775180248	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6594841	CCAGGAAACAGGGCT[G/T]AACCAGACCTGATTT	1108
rs775187139	in-del	-/C	3.29511e-05	0.00405887	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581278	TATGGCATTCAGTCA[-/C]CCCATCTCTTACCTC	1108
rs775201388	snp	C/T	1.67284e-05	0.00289205	intron-variant	CHD4	GRCh38.p7	12:6587991	GAAATTGTATTTTCC[C/T]GGTGCCACTCTTATC	1108
rs775278280	snp	C/T	0.000108237	0.00735573	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581796	TCCAGCGCCCATTAA[C/T]ATGTTCAAACTCCTG	1108
rs775280935	snp	A/G	1.6473e-05	0.00286988	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581155	CATCCTCTGAGGCAG[A/G]GGCAGGGGCCTGTGT	1108
rs775287720	snp	A/G	1.64743e-05	0.00287	synonymous-codon	CHD4	GRCh38.p7	12:6587716	GACTACCTCACCTCC[A/G]TCAGTGGCTTCATCC	1108
rs775288338	snp	C/T	1.67916e-05	0.0028975	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581675	ACAGGTGCAGGAGTG[C/T]TGGGCTGCGTGTCCC	1108
rs775293840	snp	C/T	1.64773e-05	0.00287026	missense	CHD4	GRCh38.p7	12:6593480	GAGAACTCATTCTCT[C/T]GGATGATGGCACGGC	1108
rs775294033	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6585239	ATACTATTTTTTTTA[C/G]TATAAAAGACCAAGA	1108
rs775362081	in-del	-/AAAAAAAAAA			intron-variant	CHD4	GRCh38.p7	12:6577418	CAGAGATTCTGCCTC[-/AAAAAAAAAA]AAAAAAAAAAAACAA	1108
rs775398915	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6574867	GAGTTGGCAAGCTAC[A/C]GCCTGTGGGCCAGAT	1108
rs775416082	snp	A/C	1.64741e-05	0.00286998	missense	CHD4	GRCh38.p7	12:6601654	CTGTTTTACCTGACA[A/C]ACTGGCTGAAGGCCT	1108
rs775516175	snp	A/G	1.67461e-05	0.00289357	intron-variant	CHD4	GRCh38.p7	12:6600193	CTCATGGGTTCCAAG[A/G]GGCCACAATGGCCAG	1108
rs775541121	snp	A/G	1.64727e-05	0.00286986	missense	CHD4	GRCh38.p7	12:6602401	TGGCGCTTGCTCTTA[A/G]GGATTTTAGGGTCCC	1108
rs775542136	snp	A/T	1.64923e-05	0.00287156	synonymous-codon	CHD4	GRCh38.p7	12:6592512	GTCATGCAGTTTTTT[A/T]ATCTGGTCCTCCTTG	1108
rs775582859	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6590402	TTTGATCATTGTACT[A/G]CAGTTACGTAAGTTA	1108
rs775592584	snp	C/T	4.17789e-05	0.00457031	intron-variant	CHD4	GRCh38.p7	12:6578738	TACAGTCTTTTATCT[C/T]GGGATAAAATGGCTA	1108
rs775604173	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6601785	CAGAAAGAGCAAAGT[A/C]AAGTAAGTACCTGCC	1108
rs775642086	snp	A/G	3.40275e-05	0.00412463	intron-variant	CHD4	GRCh38.p7	12:6595973	AAAAAAAAAAAAAAG[A/G]AACAACTCTATGCCT	1108
rs775645993	in-del	-/A	4.98708e-05	0.00499328	intron-variant	CHD4	GRCh38.p7	12:6600428	AAGCCCAGTTATTGG[-/A]AAAAAAACTACCTCC	1108
rs775649820	snp	C/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608109	CCCGTAATAATCAGT[C/T]TCCCACTTTCTATAC	1108
rs775658396	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6576154	ATGAGGTCAAGAGAT[C/G]GAGACCATCCTGGCC	1108
rs775734371	snp	A/G	1.65239e-05	0.00287431	missense	CHD4	GRCh38.p7	12:6598341	TGGGATCAGCATCTG[A/G]AGGCCGAGGCACTGG	1108
rs775735276	snp	C/T	4.94605e-05	0.0049727	synonymous-codon	CHD4	GRCh38.p7	12:6602487	ATCCTCTTCTGGGTC[C/T]TCTTCATTTTCTACA	1108
rs775743399	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6588991	AGTGACTCACACCTG[C/T]AACCCCAACACTTTG	1108
rs775768456	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6594109	CAAAGTGCTGGGATT[A/G]CAGGTATGAGCCACT	1108
rs775780080	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6599249	CCAGCCTGGGCAACA[C/T]AGTGAGACCCTGTCT	1108
rs775834050	snp	C/T	1.74263e-05	0.00295175	missense	CHD4	GRCh38.p7	12:6600937	TCACCGAGGATCTCT[C/T]ACGCTTGGAACCAAA	1108
rs775838192	snp	A/G	1.67326e-05	0.00289241	intron-variant	CHD4	GRCh38.p7	12:6592106	TGAGAGCCTTTCAAT[A/G]ACTAATAATGCAGTG	1108
rs775864311	snp	A/G	1.67843e-05	0.00289687	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583352	TTCTTCCTGTTTAAT[A/G]ATTTCCCGTTCTACC	1108
rs775864340	snp	C/G	1.64762e-05	0.00287016	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581272	CTTTAGTATGGCATT[C/G]AGTCACCCCATCTCT	1108
rs775981812	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6605443	CCCCAATCAGACAGG[A/G]TGGTTACAACCATAC	1108
rs776001431	snp	C/T	1.733e-05	0.00294358	missense	CHD4	GRCh38.p7	12:6602003	TCCTCCTCCTCCTTC[C/T]GCTTGGATTTGCTCT	1108
rs776068155	in-del	-/G	1.64796e-05	0.00287046	intron-variant	CHD4	GRCh38.p7	12:6577778	TATTCCTCCCCAACC[-/G]GCTCACCTTAAACCT	1108
rs776080022	snp	A/C			missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581766	TTTCCTCCACCTCAG[A/C]CAGTTCAGGCATGCT	1108
rs776098207	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6572412	GCCTGGGCAACAGAG[A/C]TAGACTCTATCTCAG	1108
rs776117782	snp	C/T	1.74184e-05	0.00295109	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606378	CCCGACGCCATCCCC[C/T]TCCGCTCCCGGCCAG	1108
rs776119157	snp	C/G	8.40866e-05	0.00648354	intron-variant	CHD4	GRCh38.p7	12:6591436	AAGCAAATGAGGATT[C/G]CTGAAACTAAACAAC	1108
rs776119274	snp	C/T	0.000115478	0.00759775	synonymous-codon	CHD4	GRCh38.p7	12:6594504	TGTCTGTACAGTTTT[C/T]CCAAGGCCCATCTCA	1108
rs776134270	snp	A/G	9.08604e-05	0.00673958	intron-variant	CHD4	GRCh38.p7	12:6598468	CAAATCATAACCATG[A/G]GAGGAGAAGGGACAG	1108
rs776192770	snp	A/C/G	3.29458e-05	0.00405857	missense	CHD4	GRCh38.p7	12:6601708	TCCTCCTCTGAGAAC[A/C/G]CGTGGTCAATGTCTT	1108
rs776200810	snp	C/G	1.64757e-05	0.00287012	synonymous-codon	CHD4	GRCh38.p7	12:6593515	CTTGTCACCCACATA[C/G]GTTACGACATACATG	1108
rs776219606	snp	C/G/T	3.29534e-05	0.00405904	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581253	ACTGGACTTACACAT[C/G/T]TGTCTTTAGTATGGC	1108
rs776221745	snp	A/G	1.64803e-05	0.00287052	missense	CHD4	GRCh38.p7	12:6573191	TGAGGGCCATGGAAG[A/G]GTGAGAAGGGTCTTC	1108
rs776297162	in-del	-/G	1.73573e-05	0.00294591	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583014	AAAGCAACAAAAAAA[-/G]CACAGCCCTCACCTT	1108
rs776302063	in-del	-/CTTCAAAATTTCGA	1.65608e-05	0.00287752	frameshift-variant	CHD4	GRCh38.p7	12:6592020	CTCGGGCATTGAGTG[-/CTTCAAAATTTCGA]GTGAGGATGTACTTG	1108
rs776309576	snp	A/G	1.64735e-05	0.00286993	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581163	GAGGCAGGGGCAGGG[A/G]CCTGTGTACACTTCA	1108
rs776317234	snp	A/C/T			intron-variant	CHD4	GRCh38.p7	12:6571915	GTGGTGAACTGAGAT[A/C/T]GCGCCATTGCTCTCC	1108
rs776328444	snp	A/G	3.38404e-05	0.00411328	intron-variant	CHD4	GRCh38.p7	12:6593637	AGAAAAAAGAGGAGA[A/G]TCAGGACTGAGGGCC	1108
rs776328603	in-del	-/CAAAAAAAAA			intron-variant	CHD4	GRCh38.p7	12:6577417	ACAGAGATTCTGCCT[-/CAAAAAAAAA]AAAAAAAAAAAAACA	1108
rs776348767	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6575559	ATAAATTCTTTGGTG[G/T]TGTTTCCTTTATCTT	1108
rs776371949	snp	A/G			synonymous-codon	CHD4	GRCh38.p7	12:6600001	AGCTTCCCACTGGAT[A/G]CCTTCCTTCTCCTGC	1108
rs776395646	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6599760	TTTGCCCCGGCTGAG[A/G]TCAGTCACTCACCGT	1108
rs776409413	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6604412	ATGAGACATTAGGCT[A/G]GACAAAGCACCATCA	1108
rs776418316	snp	G/T	6.25078e-05	0.00559017	intron-variant	CHD4	GRCh38.p7	12:6578762	ATGGCTAGATGAGTA[G/T]GGACAGGGAGGCAGG	1108
rs776444643	snp	C/T	1.8069e-05	0.00300569	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581810	ACATGTTCAAACTCC[C/T]GAACCTGTAGCAATG	1108
rs776446521	snp	A/G	1.67697e-05	0.00289561	intron-variant	CHD4	GRCh38.p7	12:6588453	AAAACACCATTAGAA[A/G]TGTCTCCTAAATTCC	1108
rs776495567	snp	A/G	3.33556e-05	0.00408371	intron-variant	CHD4	GRCh38.p7	12:6600203	CCAAGGGGCCACAAT[A/G]GCCAGACACTCACGC	1108
rs776624494	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6586823	CTGCCTCAGCCTCCC[C/G]AACACCTGGGACTAC	1108
rs776638402	in-del	-/TCCTCC	6.15296e-05	0.00554626	cds-indel	CHD4	GRCh38.p7	12:6601979	GAATCATCATCATCA[-/TCCTCC]TCCTCCTCCTCCTCC	1108
rs776684201	snp	A/C	1.65343e-05	0.00287521	intron-variant	CHD4	GRCh38.p7	12:6596148	CCACACTGCAAGTCC[A/C]GGAGAGAAAACCCTC	1108
rs776684449	snp	C/T	1.78889e-05	0.00299068	intron-variant	CHD4	GRCh38.p7	12:6592348	AAACACTCTGCAGAC[C/T]GGCAGATGTCTAAAT	1108
rs776684921	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6585307	CTAATCTTTTTGAGA[C/T]GGAGTCTGGCTCTGT	1108
rs776708445	snp	C/G	1.6476e-05	0.00287014	missense	CHD4	GRCh38.p7	12:6587543	ACTGCTATCTTCTCC[C/G]TCTTTGTTGTCTCCT	1108
rs776709332	snp	A/T	1.71117e-05	0.00292499	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583368	ATTTCCCGTTCTACC[A/T]CCTCTTCCTCCTGGG	1108
rs776762420	snp	C/T	3.47126e-05	0.00416594	intron-variant	CHD4	GRCh38.p7	12:6606242	GCCCCAGATGTCTCC[C/T]TCCCGCCATGGGCCC	1108
rs776768264	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6597739	CCACTGCACTCCAGC[C/T]TGGGCACAGAGTGAG	1108
rs776776185	snp	C/T	1.64727e-05	0.00286986	intron-variant	CHD4	GRCh38.p7	12:6595979	AAAAAAAAGAAACAA[C/T]TCTATGCCTCACCCA	1108
rs776777177	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6590739	AGCAGCAGGATCACT[C/T]GAGCCTGGGGGTGTG	1108
rs776781403	snp	A/G	1.82091e-05	0.00301732	intron-variant	CHD4	GRCh38.p7	12:6598474	ATAACCATGGGAGGA[A/G]AAGGGACAGCCCACA	1108
rs776797804	in-del	-/ACGTTCAAGCCAA	6.63757e-05	0.00576051	intron-variant	CHD4	GRCh38.p7	12:6600698	AAAGAATAAGGTTAG[-/ACGTTCAAGCCAA]GGGGAAGGACAGAGT	1108
rs776864024	snp	C/G	1.64757e-05	0.00287012	missense	CHD4	GRCh38.p7	12:6594553	GTGCCCTGAGCCCAG[C/G]AGAAGCGCAACCAAT	1108
rs776875937	snp	A/G	0.000330431	0.0128494	intron-variant	CHD4	GRCh38.p7	12:6601282	TCCCATTTGAACCCC[A/G]TTTCACCTTTGCCCT	1108
rs776879113	snp	C/G	1.66294e-05	0.00288347	intron-variant	CHD4	GRCh38.p7	12:6592582	CTTCAGAAAGAAAAA[C/G]GAAAAAAGTTATTGG	1108
rs776901924	snp	A/C	3.29723e-05	0.00406018	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581455	GAAGGTCATTTCTTC[A/C]CAGTTTGTCTCATCT	1108
rs776955797	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6589064	ACTAAGCTGGCCAAC[A/G]TGGTGAAACCCTGCC	1108
rs776959991	in-del	-/T	1.64993e-05	0.00287218	intron-variant	CHD4	GRCh38.p7	12:6577956	ACAAAACAAGGAAAG[-/T]TAAGAACCTCAAACT	1108
rs776984140	snp	C/G	1.64874e-05	0.00287113	intron-variant	CHD4	GRCh38.p7	12:6599759	TTTTGCCCCGGCTGA[C/G]ATCAGTCACTCACCG	1108
rs777012922	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6590152	GCAATGAGTCAAGAT[C/T]GCGCCACTGCACTCC	1108
rs777021265	snp	C/T	3.29527e-05	0.00405898	missense	CHD4	GRCh38.p7	12:6577873	TCATTGAGGATGGCA[C/T]AGCGTGGGTCATTCT	1108
rs777060458	snp	A/G	8.24273e-05	0.00641926	intron-variant	CHD4	GRCh38.p7	12:6591600	TGCAAAAGAAGCACG[A/G]TTTAATTATGGAAGA	1108
rs777070683	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6600132	GCAGCACCAGCATTT[C/T]CATTTCCATCCAGGC	1108
rs777153294	snp	C/G	1.6552e-05	0.00287676	synonymous-codon	CHD4	GRCh38.p7	12:6600559	CTTTTTAGTGGTTCG[C/G]AGTTTCTTGCGGCTG	1108
rs777161709	snp	C/G	0.000296467	0.0121715	synonymous-codon	CHD4	GRCh38.p7	12:6591739	CTCCTTAAGGTTCTT[C/G]AGCATTTTCTGCAGC	1108
rs777195281	in-del	-/ACAGC			intron-variant	CHD4	GRCh38.p7	12:6605774	CTTCACACAGTTCAG[-/ACAGC]ACAGCACAGAAAACC	1108
rs777228700	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6597044	GAAGGAGGAGGTGAG[C/T]GGATCACAAGGTCAG	1108
rs777237590	snp	C/T			upstream-variant-2KB	CHD4	GRCh38.p7	12:6608800	GCTTACCTCCAGCTC[C/T]TAAGTTTTGAGGAAC	1108
rs777249542	snp	C/T	1.65463e-05	0.00287626	intron-variant	CHD4	GRCh38.p7	12:6595287	AGACTGCAGCAAAGA[C/T]ACATTGTCCTACCCA	1108
rs777291017	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6596657	ATGCAAAAATTAGCC[A/G]GGCATGGTGGCAGGT	1108
rs777295505	snp	A/T	1.64844e-05	0.00287087	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581603	GCAGAAAAATAGGCC[A/T]GGACAAAAAGAGAGG	1108
rs777305313	snp	A/G	1.64749e-05	0.00287005	synonymous-codon	CHD4	GRCh38.p7	12:6587429	GGCCACTTTGAATGA[A/G]CTCAAATATTCATTC	1108
rs777330785	snp	C/T	1.66771e-05	0.00288761	missense	CHD4	GRCh38.p7	12:6602127	CCTCCTCCACAAACT[C/T]TGGCCCCTCCCCAGA	1108
rs777343633	snp	A/C/T	0.000148303	0.00861	synonymous-codon	CHD4	GRCh38.p7	12:6601341	CTCCACAGGGGGAGG[A/C/T]GGTGGTGCAACCTCA	1108
rs777378305	in-del	-/AAGT	1.64904e-05	0.00287139	intron-variant	CHD4	GRCh38.p7	12:6601786	AGAAAGAGCAAAGTC[-/AAGT]AAGTACCTGCCACCT	1108
rs777406763	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6576913	TTTCTTCCCCGATTA[C/T]ACTCAGCGTACGAGA	1108
rs777472792	in-del	-/G			intron-variant	CHD4	GRCh38.p7	12:6591299	AGAAAAAATCTCCTA[-/G]GAATAGTCCAATACA	1108
rs777491233	snp	C/G	1.66032e-05	0.0028812	synonymous-codon	CHD4	GRCh38.p7	12:6578091	CTCATAAGTCTTCTT[C/G]GTAACTGTGGCTGCC	1108
rs777500246	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6575872	GGCTATCTGCTATTT[C/T]CAGACATACTAAGCT	1108
rs777516878	in-del	-/AG	6.6036e-05	0.00574575	intron-variant	CHD4	GRCh38.p7	12:6598112	CAGCTTTGAGCGGAA[-/AG]AGAAAATCAGCCACC	1108
rs777539073	snp	C/T	1.66885e-05	0.00288859	missense	CHD4	GRCh38.p7	12:6594647	GCTCATACTTCACTG[C/T]TGGCTGAAGGATGAA	1108
rs777557119	snp	C/T	0.000164764	0.00907495	intron-variant	CHD4	GRCh38.p7	12:6591851	ATGCAAAGAAAAAAG[C/T]ATTAAAAGAAAGCCC	1108
rs777560102	snp	C/G	3.33433e-05	0.00408296	intron-variant	CHD4	GRCh38.p7	12:6600525	CAAATATACAGAAGA[C/G]AAACACACCTTTCTT	1108
rs777627101	snp	C/T	1.65277e-05	0.00287464	synonymous-codon	CHD4	GRCh38.p7	12:6594492	CAGGAAGACTGCTGT[C/T]TGTACAGTTTTCCCA	1108
rs777629271	snp	G/T	1.65239e-05	0.00287431	intron-variant	CHD4	GRCh38.p7	12:6599744	CTACACTTTCCCATT[G/T]TTTGCCCCGGCTGAG	1108
rs777629852	in-del	-/AAGAAAATGGTCCTAC	1.65094e-05	0.00287305	splice-donor-variant	CHD4	GRCh38.p7	12:6570853	AGAGGTGGTGTCAAG[-/AAGAAAATGGTCCTAC]CTGCTGTGGGGTAGG	1108
rs777670256	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6600875	GATAGAAGGTCACAT[C/T]CTTTCTATTAGACAT	1108
rs777746695	snp	A/C	1.64972e-05	0.00287199	intron-variant	CHD4	GRCh38.p7	12:6598132	AAATCAGCCACCAAG[A/C]AGCTGTGTTCATTCC	1108
rs777748998	snp	C/T	1.65029e-05	0.00287248	missense	CHD4	GRCh38.p7	12:6598003	TCTTTCGCTTTCGGC[C/T]TTTCTCTTCATCACC	1108
rs777753318	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6580442	CAGGCATGGTAGCTC[-/A]ACGCCTGTAATCCCA	1108
rs777754553	snp	C/G	1.65269e-05	0.00287457	missense	CHD4	GRCh38.p7	12:6600619	AACAGAATAGCTATT[C/G]ATACTGGCATCATCG	1108
rs777762075	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6589627	CAAAAATTAGCCGGG[C/T]GTGGTGGCGGGTGCC	1108
rs777763272	snp	A/C	1.66172e-05	0.00288242	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582881	ACGGGCCAACAGAGG[A/C]GGCAATGGCTTATCT	1108
rs777764824	snp	A/C			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582441	CTAGACCCCACAAGA[A/C]GACCCAGGTTCTCTT	1108
rs777768234	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6589915	TCAAAAGTATCTATA[C/T]TGACCAGGCACAGTG	1108
rs777793297	snp	C/T	1.64746e-05	0.00287002	missense	CHD4	GRCh38.p7	12:6573113	GCTTGTTTCCTGCCA[C/T]TGACTCCTTGGACAG	1108
rs777855904	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6586506	AAGGCAGGAGAACTG[C/T]TTAAGGCCAGGAGTT	1108
rs777873030	in-del	-/TGA			intron-variant	CHD4	GRCh38.p7	12:6571136	GTGACCAAGTAACTG[-/TGA]TGTATTGTCTTCTGT	1108
rs777898348	snp	A/T	4.94988e-05	0.00497463	intron-variant	CHD4	GRCh38.p7	12:6601573	GGAAAGGTTTAAGAA[A/T]AAAAAAAGAAAGAGA	1108
rs777924620	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	CHD4	GRCh38.p7	12:6599965	TTCCAGGATCTCCTC[A/G]CCCTCCGAATTGTCC	1108
rs777986787	snp	A/C/G	5.11089e-05	0.00505493	missense	CHD4	GRCh38.p7	12:6606351	GCCGAGCAGGGGGAC[A/C/G]GGGAGCCCAGGCCCG	1108
rs777991458	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6593996	GTGCACCACCACATC[C/T]GGCTAATTTTGTATT	1108
rs778005514	snp	A/C	3.29571e-05	0.00405924	synonymous-codon	CHD4	GRCh38.p7	12:6601761	CTGAGCAGATGATTT[A/C]GGCTCCTGCAGAAAG	1108
rs778080546	in-del	-/C	0.000100876	0.00710125	intron-variant	CHD4	GRCh38.p7	12:6591436	AAGCAAATGAGGATT[-/C]CTGAAACTAAACAAC	1108
rs778126826	snp	A/G	1.65891e-05	0.00287998	intron-variant	CHD4	GRCh38.p7	12:6587952	CTCTGCTAAAGGCCT[A/G]GAGTTGAACAGGAAA	1108
rs778144320	snp	C/G	0.000145854	0.00853849	intron-variant	CHD4	GRCh38.p7	12:6578703	CCATTGGCCCACTGA[C/G]AACTAAATGTGGGGA	1108
rs778146868	snp	C/T	1.65252e-05	0.00287443	missense	CHD4	GRCh38.p7	12:6578486	TCATCATTCAGGTCC[C/T]TGGGGGTCTCTCCAT	1108
rs778179799	snp	A/C/G	5.58689e-05	0.00528506	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606403	GGCCAGGGAATTGGC[A/C/G]CAGCTGCTCCTGCCG	1108
rs778203096	in-del	-/G	1.65482e-05	0.00287643	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581638	GAAAATGATAGGACA[-/G]GCAGACTTACCAGCA	1108
rs778223209	snp	C/G	3.2993e-05	0.00406145	missense	CHD4	GRCh38.p7	12:6596035	GCTCTGCTTGAACAG[C/G]TCGTAATCCTGGATC	1108
rs778264131	in-del	-/AA			intron-variant	CHD4	GRCh38.p7	12:6574707	TTTGTGAGAAATACC[-/AA]AAGACTTGTCTAAAA	1108
rs778322807	snp	A/T	1.65154e-05	0.00287358	intron-variant	CHD4	GRCh38.p7	12:6588291	GCTGCCTGCTGCCTC[A/T]GCTCACCTGAATGTC	1108
rs778322862	snp	A/G	1.73396e-05	0.0029444	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581738	GGTGACCCTGGCTGG[A/G]ACATCTTCTTGTTTT	1108
rs778415705	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6585972	GGGCATGGTGGTGCA[C/T]ACCTGTAATCTCAGC	1108
rs778428775	snp	C/G	1.64735e-05	0.00286993	missense	CHD4	GRCh38.p7	12:6595363	TTTCTGGAGGCCTCT[C/G]CAACTTCCGAAGCTT	1108
rs778446189	snp	C/G	1.65018e-05	0.00287239	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581621	ACAAAAAGAGAGGGA[C/G]AGAAAATGATAGGAC	1108
rs778507180	snp	C/T	1.64732e-05	0.0028699	intron-variant	CHD4	GRCh38.p7	12:6591682	CCCTAAAGCTCCCAG[C/T]CCACATGATACCTGG	1108
rs778512761	snp	A/G	3.29457e-05	0.00405854	synonymous-codon	CHD4	GRCh38.p7	12:6599902	CTTGCAGACCCGACA[A/G]AATTCCATATGGTGG	1108
rs778550943	in-del	-/A	1.65875e-05	0.00287984	intron-variant	CHD4	GRCh38.p7	12:6599723	CAATAGCCTACATAG[-/A]AAAGACTACACTTTC	1108
rs778552421	snp	A/G	3.29772e-05	0.00406048	missense	CHD4	GRCh38.p7	12:6578445	TGTTAAACATGAAAC[A/G]TTGTTTAATATTTTT	1108
rs778670261	snp	C/G	1.65811e-05	0.00287929	intron-variant	CHD4	GRCh38.p7	12:6602190	GCTGGAGCAGGGCAA[C/G]GGGGGAAGAGGGAGA	1108
rs778681183	snp	A/T	3.58352e-05	0.00423277	intron-variant	CHD4	GRCh38.p7	12:6600879	GAAGGTCACATCCTT[A/T]CTATTAGACATGGCA	1108
rs778770018	snp	A/G			upstream-variant-2KB	CHD4	GRCh38.p7	12:6609138	GCAAGGCCGAGCTCC[A/G]CACCATGGAGAATCA	1108
rs778787649	snp	A/C	1.65045e-05	0.00287263	missense	CHD4	GRCh38.p7	12:6598276	GCCTTGCCATTTCAC[A/C]AAGAACTGCCGCTCT	1108
rs778802291	snp	A/C	1.64857e-05	0.00287099	synonymous-codon	CHD4	GRCh38.p7	12:6588349	GATAATAACTGTGTC[A/C]GCAGTGGCCAGATTG	1108
rs778805396	snp	A/G	1.72928e-05	0.00294043	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583007	ATTTAGAAAAGCAAC[A/G]AAAAAAGCACAGCCC	1108
rs778830438	snp	A/G	3.29495e-05	0.00405877	synonymous-codon	CHD4	GRCh38.p7	12:6573128	TTGACTCCTTGGACA[A/G]GTGCTGATGACTTTC	1108
rs778878369	snp	C/T	1.64822e-05	0.00287068	missense	CHD4	GRCh38.p7	12:6593453	CCACCACGAATGGCA[C/T]TGTCTTCAAAGGAGA	1108
rs778888126	snp	C/T	1.79046e-05	0.00299199	intron-variant	CHD4	GRCh38.p7	12:6600890	CCTTTCTATTAGACA[C/T]GGCACCCTCCCTAAA	1108
rs778917476	snp	A/C	1.64754e-05	0.00287009	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581199	AAAAAAAACAAAAAC[A/C]AAACAGATGAAGCAG	1108
rs778952479	snp	A/C/G/T	0.000172663	0.00929009	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606408	GGGAATTGGCCCAGC[A/C/G/T]GCTCCTGCCGGCGGC	1108
rs778981993	snp	A/G	2.31136e-05	0.00339945	intron-variant	CHD4	GRCh38.p7	12:6595959	AAGACTCCATCTCAA[A/G]AAAAAAAAAAAAGAA	1108
rs779021444	in-del	-/C	1.69945e-05	0.00291496	intron-variant	CHD4	GRCh38.p7	12:6571069	GGTGAGCTGTGGTGG[-/C]CCCAGACTGAGCTCC	1108
rs779074434	snp	A/C/T	3.35611e-05	0.0040963	intron-variant	CHD4	GRCh38.p7	12:6600187	CTTCTTCTCATGGGT[A/C/T]CCAAGGGGCCACAAT	1108
rs779081069	snp	C/T	1.66272e-05	0.00288328	intron-variant	CHD4	GRCh38.p7	12:6587961	AGGCCTGGAGTTGAA[C/T]AGGAAATAAAGCCAG	1108
rs779086683	snp	A/T	1.65132e-05	0.00287339	intron-variant	CHD4	GRCh38.p7	12:6597849	AATCTCTTTAGCAGG[A/T]CTCTCCCACGGAGAC	1108
rs779107447	snp	C/G	1.72021e-05	0.0029327	intron-variant	CHD4	GRCh38.p7	12:6573280	AAGAGCTGGACAAGG[C/G]ATAAGAGGAAACGGG	1108
rs779108570	in-del	-/TC			intron-variant	CHD4	GRCh38.p7	12:6596479	ACATGGCGAAACCCG[-/TC]TCTACTAAAAAAAAA	1108
rs779115050	snp	A/C/T	1.72728e-05	0.00293872	intron-variant	CHD4	GRCh38.p7	12:6606255	CCTTCCCGCCATGGG[A/C/T]CCTTGGGGAAGATGT	1108
rs779121504	snp	C/G			missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582666	ACAAGCCACTGGGTA[C/G]TAAAAGCATCCTGAG	1108
rs779177743	snp	A/G	9.88452e-05	0.00702942	synonymous-codon	CHD4	GRCh38.p7	12:6600340	TTGCTGGCACACCTC[A/G]CAATAGTCCTGGTGG	1108
rs779190977	snp	C/T	0.000115448	0.00759675	synonymous-codon	CHD4	GRCh38.p7	12:6592476	GGCTTTGAGCCGCCG[C/T]AACATGTGCGGCCCC	1108
rs779193138	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6588779	AAGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	1108
rs779242443	snp	C/T	1.66369e-05	0.00288412	intron-variant	CHD4	GRCh38.p7	12:6601262	CCCACACTAGACACC[C/T]CCACTCCCATTTGAA	1108
rs779246604	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6575292	ATCTCTACTAAAAAT[A/G]CAAAAATTAGTCAGG	1108
rs779247968	in-del	-/C			intron-variant	CHD4	GRCh38.p7	12:6572008	GGGCATGCCTGTAGT[-/C]CCAGCTACTCAGGAG	1108
rs779298727	snp	G/T	1.64841e-05	0.00287085	intron-variant	CHD4	GRCh38.p7	12:6570713	AGAAGGAGACCCGAG[G/T]AGTCAGAATTCCAGA	1108
rs779301809	snp	A/T	1.64836e-05	0.0028708	missense	CHD4	GRCh38.p7	12:6570884	CTGCTGTGGGGTAGG[A/T]TCGGGTGCCCGGTTT	1108
rs779321114	snp	A/T	1.64754e-05	0.00287009	missense	CHD4	GRCh38.p7	12:6602468	GAGTCTCTGTTTCTG[A/T]CAAATCCTCTTCTGG	1108
rs779326131	snp	A/G	6.97083e-05	0.00590333	intron-variant	CHD4	GRCh38.p7	12:6606227	GAGTCACTCGGGAGA[A/G]CCCCAGATGTCTCCT	1108
rs779337935	in-del	-/A	3.34647e-05	0.00409038	intron-variant	CHD4	GRCh38.p7	12:6593624	GAATGACCCTTTGAG[-/A]AAAAAGAGGAGAGTC	1108
rs779356295	snp	A/C/G			intron-variant	CHD4	GRCh38.p7	12:6574348	ATGCATTCTCCTAAT[A/C/G]CTGAACATTTATGTT	1108
rs779378838	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583273	CCAGATTTCGGGCTA[A/G]ATCTTCTTGCTGCTG	1108
rs779388804	snp	G/T	1.6516e-05	0.00287362	intron-variant	CHD4	GRCh38.p7	12:6592675	CAATTATGAGCCGAT[G/T]ACAGATAAACACATA	1108
rs779392929	in-del	-/T			upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570175	TTTTTTTTTTTCCAC[-/T]TTATTTCATTTAGCC	1108
rs779422768	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6587101	CATTCAAAATTTCAT[G/T]TGTAAGGTTTAATAA	1108
rs779449232	snp	A/C/G	8.23722e-05	0.00641717	intron-variant	CHD4	GRCh38.p7	12:6591874	GAAAGCCCACATGGA[A/C/G]AAGACCCAACCCAGG	1108
rs779472833	snp	C/G/T	9.2912e-05	0.00681535	intron-variant	CHD4	GRCh38.p7	12:6578721	CTAAATGTGGGGACA[C/G/T]GTACAGTCTTTTATC	1108
rs779499007	in-del	-/GCTGTCACCAT			intron-variant	CHD4	GRCh38.p7	12:6603161	GCCCGAATCAGCCCA[-/GCTGTCACCAT]GCTGTCACCATCTCC	1108
rs779545095	snp	A/G	1.65581e-05	0.00287728	missense	CHD4	GRCh38.p7	12:6592017	CACCTCGGGCATTGA[A/G]TGCTTCAAAATTTCG	1108
rs779549418	snp	A/G	1.69908e-05	0.00291463	missense	CHD4	GRCh38.p7	12:6601018	TGGCATCAGGTACAC[A/G]AGGGCTGCCCTTGGG	1108
rs779587002	snp	A/G	3.30246e-05	0.0040634	synonymous-codon	CHD4	GRCh38.p7	12:6578476	CTTCTGTTTCTCATC[A/G]TTCAGGTCCTTGGGG	1108
rs779611372	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6603563	TTGAGAGAGGTGGGG[G/T]GGCGGGGGGGGAGAC	1108
rs779634924	snp	A/G	1.65531e-05	0.00287686	intron-variant	CHD4	GRCh38.p7	12:6595462	TCACACAGCTGCCCA[A/G]AATCCTTTTCTATAG	1108
rs779666067	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6588090	CCTTTTGCACCCCTG[C/T]CTCCAGACACCACCC	1108
rs779691620	snp	C/T	1.64866e-05	0.00287106	utr-variant-3-prime	CHD4	GRCh38.p7	12:6570675	GTATCAGTCTGCATC[C/T]TCACTGCTGCTGGGC	1108
rs779699534	snp	A/G			intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582371	GCATTATCACAGGCA[A/G]TAACTATGGCTCCAC	1108
rs779705073	snp	C/T	1.96585e-05	0.0031351	utr-variant-5-prime	CHD4	GRCh38.p7	12:6606411	AATTGGCCCAGCTGC[C/T]CCTGCCGGCGGCCTG	1108
rs779720833	snp	A/T	1.64732e-05	0.0028699	missense	CHD4	GRCh38.p7	12:6602377	AGTCACCCACTCACC[A/T]CCTTTTTTTGGCGCT	1108
rs779744206	snp	C/G	1.65075e-05	0.00287289	synonymous-codon	CHD4	GRCh38.p7	12:6598318	CAAGGGCTTTGGGGA[C/G]GGCGTGTTGGGATCA	1108
rs779762991	snp	A/G	1.68735e-05	0.00290456	intron-variant	CHD4	GRCh38.p7	12:6593632	CTTTGAGAAAAAAGA[A/G]GAGAGTCAGGACTGA	1108
rs779785242	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6577569	CACTAGTGTGTCACT[C/G]ATTGGACACATAGTC	1108
rs779819284	snp	A/G	3.58237e-05	0.00423209	intron-variant	CHD4	GRCh38.p7	12:6600886	ACATCCTTTCTATTA[A/G]ACATGGCACCCTCCC	1108
rs779830178	in-del	-/ATC	0.00036623	0.013527	cds-indel	CHD4	GRCh38.p7	12:6601965	TCCAGGCACCTTTGA[-/ATC]ATCATCATCATCATC	1108
rs779888564	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6579094	CAGCAGCAGGCAGAT[C/G]ACTTGAGGTCAGGAG	1108
rs779901873	snp	C/T	3.32723e-05	0.00407861	intron-variant	CHD4	GRCh38.p7	12:6591456	AACTAAACAACTCCT[C/T]CTCTCTCACCATTGA	1108
rs779921079	snp	C/G	1.6473e-05	0.00286988	missense	CHD4	GRCh38.p7	12:6602453	TCTTCTTGAGCTTTG[C/G]AGTCTCTGTTTCTGA	1108
rs779943343	snp	C/T	1.64741e-05	0.00286998	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581332	ATTTAACCTCCTTTT[C/T]TCCTTCTATGCTCTC	1108
rs779952668	snp	C/G	1.77354e-05	0.00297781	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582587	GAAGCCCTTGCTCTA[C/G]ATCAGTCCACTCCAG	1108
rs779959446	snp	A/G	1.72246e-05	0.00293462	intron-variant	CHD4	GRCh38.p7	12:6594447	AAAACTATCCACCCC[A/G]GATTTCCTTACCTCC	1108
rs779999675	snp	G/T	3.64339e-05	0.00426797	missense	CHD4	GRCh38.p7	12:6602043	TCTTAGGTCCAAGCT[G/T]CTTCTTCTTCTTCTT	1108
rs780031376	snp	A/G	1.65633e-05	0.00287774	intron-variant, upstream-variant-2KB, synonymous-codon	CHD4, SCARNA11	GRCh38.p7	12:6583178	GCCCATGGGTGGGGG[A/G]CGGGGCCGGCCACAC	1108
rs780033123	snp	A/C	3.29582e-05	0.00405931	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581220	GATGAAGCAGACAGG[A/C]CAGCAACTAAAAGGA	1108
rs780076025	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6602767	TCTCCCGTTCCTACC[A/G]GTCCTCTAGATGTTC	1108
rs780128289	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6590636	TCAGCCTGGGCAACA[C/T]GGCAAGACCCCATCT	1108
rs780147580	snp	C/T	4.95193e-05	0.00497566	missense	CHD4	GRCh38.p7	12:6578906	CCTCCACCTTCTCTA[C/T]ATCAGCAGCACCTAG	1108
rs780205594	snp	A/G	5.21626e-05	0.00510672	intron-variant	CHD4	GRCh38.p7	12:6606236	GGGAGAGCCCCAGAT[A/G]TCTCCTTCCCGCCAT	1108
rs780227031	snp	C/G	1.6661e-05	0.00288621	missense, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6582222	ACACCATCAGCAAAG[C/G]TCTCAGCCCCATCTG	1108
rs780243170	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6593667	CCCAGCACACTGCAA[C/T]CCCAGCGAACACCCA	1108
rs780246528	in-del	-/T	1.64874e-05	0.00287113	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581458	GTCATTTCTTCCCAG[-/T]TTTGTCTCATCTTAA	1108
rs780281349	snp	C/T	1.64958e-05	0.00287187	missense, intron-variant	CHD4	GRCh38.p7	12:6600384	CATCCACAGCAGTCA[C/T]CTCCTCCTCGCCTGG	1108
rs780311117	snp	A/G	1.65018e-05	0.00287239	intron-variant	CHD4	GRCh38.p7	12:6601564	AGAGCAGAGGGAAAG[A/G]TTTAAGAATAAAAAA	1108
rs780385537	snp	C/T			upstream-variant-2KB, downstream-variant-500B	NOP2, CHD4	GRCh38.p7	12:6569713	AACTTAGCAAGAAAA[C/T]CCCCCTCAGCCTTCC	1108
rs780391653	snp	A/G	3.3006e-05	0.00406226	intron-variant	CHD4	GRCh38.p7	12:6597859	GCAGGACTCTCCCAC[A/G]GAGACTGCCCGTCTC	1108
rs780400167	snp	C/T	1.65141e-05	0.00287346	intron-variant	CHD4	GRCh38.p7	12:6599751	TTCCCATTTTTTGCC[C/T]CGGCTGAGATCAGTC	1108
rs780411006	snp	A/G	3.29457e-05	0.00405854	synonymous-codon	CHD4	GRCh38.p7	12:6587510	CCGTTCAATGGCCTT[A/G]TCATCGTAGTGGATA	1108
rs780413744	snp	A/C/T	6.80521e-05	0.00583286	missense	CHD4	GRCh38.p7	12:6606297	GGTGGGGGCAGGCTG[A/C/T]TGTTCAAAAGTGCAT	1108
rs780420166	in-del	-/CT			intron-variant	CHD4	GRCh38.p7	12:6590457	AACAGTATACATGAA[-/CT]CTCTCTGCTGTTTTG	1108
rs780477570	snp	A/G	1.67312e-05	0.00289229	intron-variant	CHD4	GRCh38.p7	12:6600511	ACCTCATCCCATCAC[A/G]AATATACAGAAGAGA	1108
rs780481387	snp	A/C	1.65037e-05	0.00287256	missense	CHD4	GRCh38.p7	12:6596133	CGTGGCCCTTCTTGT[A/C]CACACTGCAAGTCCA	1108
rs780484483	snp	A/C/G/T	8.28559e-05	0.00643605	intron-variant	CHD4	GRCh38.p7	12:6601273	CACCCCCACTCCCAT[A/C/G/T]TGAACCCCATTTCAC	1108
rs780486658	snp	A/G	1.64863e-05	0.00287104	synonymous-codon	CHD4	GRCh38.p7	12:6592713	GAACCTCTCGGGGGT[A/G]AGAAAGTTGAGCAGA	1108
rs780513349	snp	A/C	1.65622e-05	0.00287764	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581012	CTGTCTCAAAACAAA[A/C]AAACAAACAAAAAAA	1108
rs780524514	snp	A/G	1.66988e-05	0.00288949	intron-variant	CHD4	GRCh38.p7	12:6571041	TTCAGAACTGCATAG[A/G]GAGAAAAAGAGGTGG	1108
rs780541459	in-del	-/AAAACACCCACACAAAAAACT	3.52622e-05	0.00419879	intron-variant	CHD4	GRCh38.p7	12:6594417	TAAGGCTTCAAACAC[-/AAAACACCCACACAAAAAACT]ATCCACCCCAGATTT	1108
rs780557518	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6574587	CCTAGTGTCAGCCAG[C/T]AGTTCTATGCAGATG	1108
rs780610876	in-del	-/AAAAA			intron-variant	CHD4	GRCh38.p7	12:6596487	AAACCCGTCTCTACT[-/AAAAA]AAAAAAAAAAAATTA	1108
rs780618370	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6584674	TAGGCATGAGCCACC[A/G]TGTCTGGCCCTTTTG	1108
rs780624598	snp	C/T	1.64819e-05	0.00287066	missense	CHD4	GRCh38.p7	12:6570892	GGGTAGGTTCGGGTG[C/T]CCGGTTTGCCAGGCG	1108
rs780647359	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6588222	CTAATTCCAGATGGT[A/G]GAGCCCTCATAGAGG	1108
rs780671489	in-del	-/AA			intron-variant	CHD4	GRCh38.p7	12:6601918	AGGAAACAAAAAGAC[-/AA]AAGTTTAACAGTACA	1108
rs780688247	snp	A/G	1.75274e-05	0.0029603	intron-variant	CHD4	GRCh38.p7	12:6598438	ACACTGAGAGAAAAA[A/G]AGACAACTTAATCTC	1108
rs780693165	snp	G/T	1.64746e-05	0.00287002	synonymous-codon, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6583214	TCGGTCCTCCTGGGA[G/T]CCATCATTGTAGTTG	1108
rs780725564	snp	A/T	1.64855e-05	0.00287097	missense	CHD4	GRCh38.p7	12:6570880	CTACCTGCTGTGGGG[A/T]AGGTTCGGGTGCCCG	1108
rs780785855	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6574844	GTACCTCAAATCCAG[G/T]AAGTCAGGAGTTGGC	1108
rs780818001	in-del	-/A			intron-variant	CHD4	GRCh38.p7	12:6595972	AAAAAAAAAAAAAAG[-/A]AAACAACTCTATGCC	1108
rs780818304	in-del	-/T			upstream-variant-2KB, utr-variant-3-prime	NOP2, CHD4	GRCh38.p7	12:6570158	CTTTTGGTTTTTTCC[-/T]TTTTTTTTTTTTCCA	1108
rs780861805	snp	G/T	1.6516e-05	0.00287362	intron-variant	CHD4	GRCh38.p7	12:6602549	AGATCAATAGCAAAA[G/T]GTTAGGCCCTAATCC	1108
rs780882752	snp	C/T	1.66521e-05	0.00288544	synonymous-codon	CHD4	GRCh38.p7	12:6594477	CTTGTAAAGGGAATA[C/T]AGGAAGACTGCTGTC	1108
rs780910406	snp	A/G	3.29554e-05	0.00405914	synonymous-codon	CHD4	GRCh38.p7	12:6591527	ACCATCGATGCGTTC[A/G]TATTTATAACCTTCA	1108
rs780966982	snp	A/G	1.65094e-05	0.00287305	synonymous-codon	CHD4	GRCh38.p7	12:6598324	CTTTGGGGAGGGCGT[A/G]TTGGGATCAGCATCT	1108
rs780974871	in-del	-/CT			intron-variant	CHD4	GRCh38.p7	12:6602749	CCAGACCCCTGCCTC[-/CT]CTCTCCCGTTCCTAC	1108
rs780987215	snp	A/G	1.64923e-05	0.00287156	synonymous-codon	CHD4	GRCh38.p7	12:6594612	GGTTCCACCTGTAGC[A/G]TCCAGGTACTCTGGC	1108
rs781058155	snp	C/T	1.66952e-05	0.00288917	intron-variant	CHD4	GRCh38.p7	12:6601251	GACATCTTAAGCCCA[C/T]ACTAGACACCCCCAC	1108
rs781066880	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6587137	ATAGGAGAAAATGAC[A/G]TTCTGGTAAAGAGCC	1108
rs781079086	snp	A/T	1.65102e-05	0.00287312	intron-variant, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581029	AACAAACAAAAAAAA[A/T]GTGGATACCTTTACC	1108
rs781138057	snp	A/G	0.00140846	0.0264999	missense	CHD4	GRCh38.p7	12:6600594	TACTACGGCTGGTGG[A/G]ACCATCAGAAACAGA	1108
rs781144738	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6590096	TCAGCTACTCAGGAG[A/G]CTGAGACAGGAGTAT	1108
rs781157992	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6599609	TGAAGTTAGTCCTAT[A/G]TTTTCCCAGGACAAA	1108
rs781165575	snp	A/C	1.6686e-05	0.00288838	intron-variant	CHD4	GRCh38.p7	12:6600522	TCACAAATATACAGA[A/C]GAGAAACACACCTTT	1108
rs781169311	in-del	-/C			intron-variant	CHD4	GRCh38.p7	12:6580219	TGACAGAGTGAGACT[-/C]CCATCTCGAAAACAA	1108
rs781178939	snp	A/G	1.64757e-05	0.00287012	missense	CHD4	GRCh38.p7	12:6577835	CTAAGAAATTGCCAC[A/G]GTTCATTTCACCCTT	1108
rs781255920	snp	A/C	1.71249e-05	0.00292612	missense	CHD4	GRCh38.p7	12:6602060	TTCTTCTTCTTCTTG[A/C]CAGGAGTATAGTCGC	1108
rs781271594	snp	C/G	1.69372e-05	0.00291004	intron-variant	CHD4	GRCh38.p7	12:6571065	GAGGTGGTGAGCTGT[C/G]GTGGCCCAGACTGAG	1108
rs781312737	snp	C/G	1.7013e-05	0.00291654	missense	CHD4	GRCh38.p7	12:6606299	TGGGGGCAGGCTGTT[C/G]TTCAAAAGTGCATCC	1108
rs781341074	snp	C/T	1.64947e-05	0.00287177	missense	CHD4	GRCh38.p7	12:6601382	CCATGCTCTCCACCA[C/T]AGCTACCGCTGCTGC	1108
rs781360267	snp	A/C	3.29549e-05	0.00405911	synonymous-codon	CHD4	GRCh38.p7	12:6592743	ATGAAACAACTCTTC[A/C]AGATTGTTTTGTAAT	1108
rs781396205	snp	C/T	3.29451e-05	0.00405851	missense, downstream-variant-500B	CHD4, SCARNA11	GRCh38.p7	12:6581113	CCACTTTCTCCTCTC[C/T]CTCAGGGGGTTCAAC	1108
rs781398794	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6585574	GGCGTGAGCCACCAC[A/G]TCTGGCCCAATTCTA	1108
rs781416352	in-del	-/TTA	4.97108e-05	0.00498527	intron-variant	CHD4	GRCh38.p7	12:6588268	AGCATAACATGTTAC[-/TTA]TTAAGGCTGCCTGCT	1108
rs781428370	snp	C/G	1.70095e-05	0.00291625	missense	CHD4	GRCh38.p7	12:6606345	CTGCCCGCCGAGCAG[C/G]GGGACGGGGAGCCCA	1108
rs781443639	snp	G/T			intron-variant	CHD4	GRCh38.p7	12:6602902	AATGAAAGATCCTAC[G/T]CAGAAGGCAAAAACT	1108
rs781451739	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6571301	AGCTTATTCGTTTTT[C/T]CTCTTCTCTACCTTC	1108
rs781474417	in-del	-/GA	3.29723e-05	0.00406018	intron-variant, nc-transcript-variant	CHD4, SCARNA11	GRCh38.p7	12:6581531	CGGCCCTCCTAAACT[-/GA]GAGGGAATTGCTGTG	1108
rs781517431	snp	A/C	3.29462e-05	0.00405857	synonymous-codon	CHD4	GRCh38.p7	12:6595379	CAACTTCCGAAGCTT[A/C]ACCTTCTTGAGCTTC	1108
rs781538095	snp	A/G	1.64955e-05	0.00287184	synonymous-codon	CHD4	GRCh38.p7	12:6593111	ACTGATTGTTCTTCA[A/G]CCGATGGGCTTCATC	1108
rs781539379	snp	A/G	1.6501e-05	0.00287232	intron-variant	CHD4	GRCh38.p7	12:6601563	AAGAGCAGAGGGAAA[A/G]GTTTAAGAATAAAAA	1108
rs781559340	snp	C/T	1.6513e-05	0.00287336	intron-variant, upstream-variant-2KB	CHD4, SCARNA11	GRCh38.p7	12:6581628	GAGAGGGACAGAAAA[C/T]GATAGGACAGGCAGA	1108
rs781615033	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6597436	ACGACACTGCACTCA[A/C]GCCTGGGCAACACAG	1108
rs781640207	snp	A/G	1.64988e-05	0.00287213	intron-variant	CHD4	GRCh38.p7	12:6587668	TCCCTAACCTTTAGA[A/G]AGGCCAAGCCCCACA	1108
rs781640400	snp	A/C	1.69143e-05	0.00290807	intron-variant	CHD4	GRCh38.p7	12:6600048	TTCAGATTATTACCC[A/C]CACCCGCCCACCGCA	1108
rs781660578	snp	C/G	0.00033399	0.0129183	missense	CHD4	GRCh38.p7	12:6573099	GACTGCATTGGCTGG[C/G]TTGTTTCCTGCCATT	1108
rs781661144	snp	A/G	1.67049e-05	0.00289002	intron-variant	CHD4	GRCh38.p7	12:6578156	AGGAGGAATTTAGGG[A/G]AGGTTGGGGGTGGGG	1108
rs781676537	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6584920	GTTTCTGATTGAACA[C/G]TACGGTACACAGACC	1108
rs781766054	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6598518	CAAAGGACGATTCAG[A/G]TCTCATTTCAGACCT	1108
rs796171176	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6597700	GAATCTGGGAGGCAG[A/C]GGTTGCAGTGAGCCG	1108
rs796226475	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6592070	TTCCTACATGGGCAA[A/G]GTAGAAAGACAGGTT	1108
rs796254830	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6585697	GGGAGGCTGAGGCAA[C/G]AGAACTGCTTGAACC	1108
rs796336890	snp	A/G			intron-variant	CHD4	GRCh38.p7	12:6579721	GTGCCACTGCACTCC[A/G]GCCTGGGTGACAGAG	1108
rs796376323	snp	C/T			intron-variant	CHD4	GRCh38.p7	12:6586906	TTTCACCGTGTTGGC[C/T]GGGCTGGTCTCAAAC	1108
rs796475197	in-del	AAA/C			intron-variant	CHD4	GRCh38.p7	12:6591141	AAAAAAAAAAAAAAA[AAA/C]AAAAAAACCTAGTAG	1108
rs796517079	snp	C/G			intron-variant	CHD4	GRCh38.p7	12:6584613	GGTCTCCAACTCCTG[C/G]GCTCAAACGACCCTC	1108
rs796764752	in-del	-/AACAAC			intron-variant	CHD4	GRCh38.p7	12:6580230	AGACTCCATCTCGAA[-/AACAAC]AACAACAACAACAAC	1108
rs796817657	snp	A/C			intron-variant	CHD4	GRCh38.p7	12:6591132	CATCTCAAAAAAAAA[A/C]AAAAAAAAAAAAAAA	1108

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