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

CHD3

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs553972625	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7911280	TAGAGAGTGGGAACA[C/T]GTGTTCAATCATGTA	1107
rs554081431	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7910772	GTGGAGTGTGGCTCA[C/T]AATGTCTCTCCTACA	1107
rs554109948	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7890439	ATCTCCAAAAAAAAA[A/G]AGGAGATAAAAAATT	1107
rs554116857	snp	A/G	0.00119737	0.0244387	intron-variant	CHD3	GRCh38.p7	17:7895764	CTCAGATATAGCATA[A/G]CCTTTCCTAACTTCA	1107
rs554141813	snp	A/G	0.000131789	0.00811648	intron-variant, missense	CHD3	GRCh38.p7	17:7889089	GACTGTGTTGGGGTG[A/G]CAGGATGCCTGGTAA	1107
rs554265399	snp	C/T	0.000319076	0.0126268	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905625	CCCACCCTCAGGGCG[C/T]AGACAGTCAAAGAGG	1107
rs554278155	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912423	CAGGTTCCTGGAAGA[C/T]TTCTACTACCCTCCC	1107
rs554325814	in-del	-/A			intron-variant	CHD3	GRCh38.p7	17:7890430	CAAGACTCCATCTCC[-/A]AAAAAAAAAAGGAGA	1107
rs554359758	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CHD3	GRCh38.p7	17:7911872	CCTCCCACACTGCCA[A/G]GTATACACAACTTCC	1107
rs554431565	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7898298	GATCTGGCTGAGTAG[C/T]GGAGAAGAGGATGTT	1107
rs554549070	in-del	-/C	0.000799476	0.0199775	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905737	GTGTTCCTGAGTTCT[-/C]CCAAGAGGGCATGAG	1107
rs554592647	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7890462	AAAAAATTAGTTACT[A/G]TCACAGGATTGTTGT	1107
rs554619181	snp	A/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7896398	ATCCATCCTTTTTCT[A/T]TTTTTTTCTATTTTT	1107
rs554630277	snp	A/G	0.00199481	0.0315187	intron-variant	CHD3	GRCh38.p7	17:7891738	TGGTGGCACATGCCT[A/G]TAATCCCAGCTACTC	1107
rs554859615	snp	A/G	5.10782e-05	0.00505336	intron-variant	CHD3	GRCh38.p7	17:7911002	TTCCTACCCCCTGCT[A/G]CTCACACTCCTCCTT	1107
rs554876016	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904354	GGAGACCGGATTGGG[C/T]TGACGCAGCAGAGTA	1107
rs555142389	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7903724	CCCGGGGAAAAAGCC[C/T]TCTCTAGGGCTCCTG	1107
rs555256217	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7887852	GACCGAGGTTGGGAC[G/T]TAGATTTGCTTTATT	1107
rs555277008	snp	C/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7910788	AATGTCTCTCCTACA[C/G]CTTCTTTCCTCTCAC	1107
rs555553165	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883988	GAGTACTGATTAATG[C/T]CCCCCCTCAAATATT	1107
rs555583815	snp	G/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7894668	CATCTCTTTCCCCCT[G/T]GGTTTCACTTACCCT	1107
rs555731106	snp	A/C	0.0240643	0.107019	missense	CHD3	GRCh38.p7	17:7909198	GGGCGGCCTACCTGA[A/C]CCTGTCGCAGGAGCC	1107
rs555797727	snp	A/G	0.0023933	0.0345097	intron-variant	CHD3	GRCh38.p7	17:7901683	GCCTAGCTAATTTTT[A/G]TATTTTTAGTAGAGA	1107
rs555887897	snp	A/G			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888746	CGCGCGTGCGCGCGC[A/G]TGCTTTTGAGAAGGC	1107
rs555984573	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886446	CTTCAAAACGGCCAA[C/T]TCCGGGCTCTTTGTA	1107
rs556091139	snp	A/C/G	3.33039e-05	0.00408055	intron-variant	CHD3	GRCh38.p7	17:7910820	GACTATGAACTAACT[A/C/G]CAACTTCTGCTTCCT	1107
rs556208480	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7911117	AGAGTTGTTCTAGGC[C/T]GTCCCCCCACCCATC	1107
rs556369795	snp	A/G/T	3.29523e-05	0.00405898	intron-variant, missense	CHD3	GRCh38.p7	17:7889003	TTTCTCCTGTGTGAT[A/G/T]AAGGCGGCAGACACT	1107
rs556409323	snp	C/T	0.00279162	0.0372561	intron-variant	CHD3	GRCh38.p7	17:7902178	GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG	1107
rs556461264	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888429	TTCCCATCTTGCATC[C/G]GCTGCCTCTCTCTGT	1107
rs556515494	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886483	TCATATTGATCCGTG[C/T]GGCTTCTGTGGCAAA	1107
rs556867944	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7900480	TGAGCTGGTAGAGGA[C/T]TAATCTGAGGTGGTA	1107
rs557215278	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7891727	TTAGCTGGGCGTGGT[G/T]GCACATGCCTGTAAT	1107
rs557576969	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7891896	AATAGTGCCGATGTA[C/T]TTTGTTTTGGGGAGA	1107
rs557605229	snp	A/G	0.000148966	0.00862907	intron-variant	CHD3	GRCh38.p7	17:7899247	CGCCTGGACTGGGGA[A/G]GTGGGGAGGGGGAAG	1107
rs557636530	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883475	ACAATTGGAGGAGGG[A/G]AAAGCGAGGGAAAGG	1107
rs557660969	snp	C/T	0.00119737	0.0244387	intron-variant	CHD3	GRCh38.p7	17:7891409	TCTCTCTAGACTGGA[C/T]CTGAGAGATACCATC	1107
rs557661825	snp	C/T	5.52644e-05	0.00525634	intron-variant	CHD3	GRCh38.p7	17:7893608	TGTCATCTCACCTTC[C/T]AAACTGCATGTCTTC	1107
rs557802726	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	CHD3	GRCh38.p7	17:7887761	GGCCCCCGCCTCTCT[C/T]CTCCCTGCCTCCCTG	1107
rs557975582	snp	A/C	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7902000	CTCTGGGTCTACTCA[A/C]CAGAAAACTGCACAT	1107
rs558199100	snp	C/T	4.87567e-05	0.0049372	intron-variant	CHD3	GRCh38.p7	17:7908390	CTCTTCTGTCTGCTG[C/T]CTTCTTTGCAGAGCT	1107
rs558271516	snp	A/G	0.000798403	0.0199641	intron-variant	CHD3	GRCh38.p7	17:7892027	TCCTCTTCTATAAAC[A/G]GGGAATAATAATATA	1107
rs558397252	snp	C/G	0.0023933	0.0345097	intron-variant	CHD3	GRCh38.p7	17:7892609	TCAAGCAATTTTTCT[C/G]CCTCAGCCTCCCGAG	1107
rs558614795	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7896459	TGCCTAGGCTGGAGT[A/G]CAGTGGCACGATCTT	1107
rs558647621	snp	A/G	0.000798403	0.0199641	intron-variant	CHD3	GRCh38.p7	17:7898386	TGGGAAAAAGGAAAT[A/G]TGGGAAAATCTAGGT	1107
rs558729972	in-del	-/GGAGAGGT/GGGAGAGG	0.00319098	0.0398384	upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7882888	GCCAGCAGTTACACT[-/GGAGAGGT/GGGAGAGG]GGAGAGGTAGAGGAA	1107
rs558730025	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7890070	GAATTCAAGAGTCCA[A/G]CATTCCTCTGTCTAG	1107
rs559016040	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7892293	CGTCCTACGGAAGCC[C/T]ATCTTCAGGGCCCAT	1107
rs559100132	snp	C/T	0.000798403	0.0199641	intron-variant	CHD3	GRCh38.p7	17:7896593	TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT	1107
rs559132295	snp	A/G	0.00119737	0.0244387	intron-variant	CHD3	GRCh38.p7	17:7891614	GCCTGTAATCCAAGC[A/G]CTTTGGGAGGCCAAG	1107
rs559285017	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884108	CACTTCAGTACACAA[A/G]GAAAATATCTCTATT	1107
rs559313061	snp	A/C	0.0107246	0.0724382	intron-variant	CHD3	GRCh38.p7	17:7901834	CTGTTCTTAAGGTTG[A/C]TGGAAGTTGAGGTCC	1107
rs559322845	snp	C/T	4.99097e-05	0.00499524	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904597	GCAAGTTAACTACAA[C/T]GATGCTGCTCAGGAA	1107
rs559649610	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7892730	TCCATCTCTTGACCT[C/T]GTGATCCTCCCACCT	1107
rs559842563	snp	G/T	0.000399281	0.0141238	missense	CHD3	GRCh38.p7	17:7911510	GAAGGAGAAGGAAAT[G/T]GTGGGGGCATTGGTG	1107
rs560011682	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7890230	GAGGTCAGGAGTTCG[C/T]GACAAGCCTGGCCAA	1107
rs560185295	snp	A/G	0.00159617	0.0282053	intron-variant	CHD3	GRCh38.p7	17:7895994	ACTTTGGGAGGCCGA[A/G]GTGGGCGGATCACCT	1107
rs560250382	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7893020	GCCCTGGGCTCAAGC[A/G]ATCCTCCTGCTTCAG	1107
rs560445269	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7901762	GTGATCTGCCCGCCT[C/T]GGTCTCCCAAAGTGC	1107
rs560445538	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7909697	GTGAATGCACCATAC[A/G]GATCCCTGGCTGTGA	1107
rs560604432	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7887992	GCACCACCCCTGGCT[A/G]GTGGTGGCCGAGGCC	1107
rs560685373	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7892387	AAGGTGGAATGTATG[C/T]GAAAGGGTTTTATGA	1107
rs560874382	snp	A/C	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7911307	TGTAGCACAAAGTGG[A/C]ATCTCAGGGAAAGGG	1107
rs560940001	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904726	GCCTAGAAGTCAGAG[C/T]CTTCCTCTGCTAAAA	1107
rs560993505	snp	C/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7896768	CATTCAAGCGATTCT[C/G]CTGCCTCAGCCTCCT	1107
rs561082386	snp	A/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7896025	GAGGTCAGGAGATCG[A/T]GACTATCCTGGCTAA	1107
rs561272668	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7894363	CTTCTCCCTCTCTCT[C/T]TCCATCTCCCCCTGC	1107
rs561278276	snp	A/C/T	0.000116496	0.00763133	missense, synonymous-codon	CHD3	GRCh38.p7	17:7910878	CCTACGCTACACCTC[A/C/T]GGGGTACGGGGCGGC	1107
rs561347195	in-del	-/T/TT			downstream-variant-500B	CHD3, LOC284023	GRCh38.p7	17:7913168	GAAGCAAAGGCACAC[-/T/TT]TTTTTTTTTTTTTTT	1107
rs561455227	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904292	ATGGCATGGAACATG[C/T]GCAATGTCCAGAAAA	1107
rs561460390	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903150	TCCGGGGTCAGAAAT[A/G]AATCTCTTCTGGGAG	1107
rs561672253	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7908926	GGTTAACACCTTCAG[A/G]GCTGAGGTGATACCT	1107
rs561948925	snp	A/C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886107	TCACTGTCACTCACT[A/C/T]TCTCGCTGAAACCAC	1107
rs562199444	snp	A/G	6.78012e-05	0.00582203	intron-variant	CHD3	GRCh38.p7	17:7901042	CCATTCTCAGAAAAC[A/G]TGGGTGGGGAGTAGT	1107
rs562290271	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7900114	AAACAACAAAAATTC[C/T]GGGGATTTTCTGTAG	1107
rs562460634	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903243	GGCCACTCCCCTGAC[A/C]CACCCGCCACTTTCT	1107
rs562550511	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7910038	ACCTCCCATGCCTCC[C/T]GACTATTTCCTCCCC	1107
rs562618883	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7902354	TTGAACCCAGGAGTG[A/G]AGGTTGCAGTGAGCA	1107
rs562699327	snp	C/T	1.64871e-05	0.00287111	intron-variant	CHD3	GRCh38.p7	17:7908676	TAAATTCCTTGATGG[C/T]TCCTTTTCCTTCATT	1107
rs562873991	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7887906	GTTCTCGCTTTGCCT[A/C]TCCCGCCACCGACGC	1107
rs563092571	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7889891	TTCTGAAGCCAGGGA[A/G]GCTTGATCCCCCGGG	1107
rs563110351	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7901710	GAGACGGGATTTCAC[C/T]ATGTTGGTCAGGATG	1107
rs563133464	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7882905	GAGAGGTAGAGGAAT[A/G]ACCCAGAGAGAAATG	1107
rs563271582	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7891774	GCTAAGGCAGGAGAA[C/T]CGCTTGAACCCGGGA	1107
rs563545591	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7898825	GCCCTTCCCCATGGT[A/G]CTGCTGGATATTGTC	1107
rs563625386	snp	C/T	0.000798403	0.0199641	intron-variant	CHD3	GRCh38.p7	17:7899648	CACCTTTCTCCTCTT[C/T]CTCCACCTGTCCTCC	1107
rs563753896	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	CHD3	GRCh38.p7	17:7912113	TGTTACCGTCCCCTA[A/C]CTCTCCCCACGTGGA	1107
rs563758726	snp	C/T	1.66167e-05	0.00288237	intron-variant	CHD3	GRCh38.p7	17:7908853	GAGGGAGGAAAGGAG[C/T]GGGTTATAGACGGGC	1107
rs564008487	snp	A/C	0.0023933	0.0345097	synonymous-codon, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885049	GCCGCCGCCGCCGCC[A/C]CCGCTGCCCCCGCCG	1107
rs564286378	in-del	-/AGA	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888216	CACGCACACAGTCCT[-/AGA]GTGTCTTCCTGCACA	1107
rs564331058	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7892286	CACACTCCGTCCTAC[A/G]GAAGCCCATCTTCAG	1107
rs564388175	snp	A/C			utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912244	TTGGGAATGTTCCCC[A/C]CTCCCTAGGGACCAA	1107
rs564488868	snp	A/G	0.000399281	0.0141238	synonymous-codon	CHD3	GRCh38.p7	17:7900684	CTTTAAGAACATGCC[A/G]GCCAAGACAGAGCTC	1107
rs564632229	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	CHD3, LOC284023	GRCh38.p7	17:7913214	GGTCAGATCTGTCTA[A/G]CTTACCAAAGATTTG	1107
rs564689440	snp	G/T	0.000228611	0.0106889	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906260	TCCTAGCCTCACATT[G/T]ACTTGACCACAATAA	1107
rs564692781	snp	A/G	1.64732e-05	0.0028699	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905150	GAGGATGAAGACTTC[A/G]ATGAACGTCCTGAAG	1107
rs564831092	snp	C/T	0.000332973	0.0128987	intron-variant	CHD3	GRCh38.p7	17:7897069	CTCTTTCCCTTTTTT[C/T]TGTGCCCTGCTAGCT	1107
rs564861312	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7891128	GGAGGTCCTGGACCC[C/T]TTGGAATCTGATGAA	1107
rs565266191	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888690	CAGGTACAGGCCATC[C/T]TCTGGATTTGTGGGC	1107
rs565470849	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7895963	GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGT	1107
rs565505499	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912383	TACAATGGGCCAGAT[A/G]TGGTGGAAGCCCAGC	1107
rs565697052	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904888	GGAGAAGCAGAGGGG[C/T]CCAGAGACTGAAGGT	1107
rs565851075	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7890474	ACTATCACAGGATTG[G/T]TGTGAAGATTAAAAG	1107
rs566174174	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912446	ACCCTCCCTCCTCAA[A/G]GCCTGGATACAGACT	1107
rs566221282	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	CHD3, NAA38	GRCh38.p7	17:7886990	GAAATGAAAACCCAC[C/T]TCCCCTCTCCCCCTG	1107
rs566341939	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888835	TAGATGAATGGGTCA[C/G]GATATCTGGAACAAA	1107
rs566388945	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7898423	CAGTGGGAAGTAGGT[A/C]TGGAATGGGTTCAGA	1107
rs566607044	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7895269	CCTTGTGGGACCCCT[A/G]TCTTCTCATCTAACA	1107
rs566634042	snp	C/T	6.60273e-05	0.00574537	synonymous-codon	CHD3	GRCh38.p7	17:7902711	CCTGAGGCAGGAGGC[C/T]ATCGATCGGTTTAAT	1107
rs566702147	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7910091	GCTCTTCCAGTATGA[A/G]ATGTTCTGACAACTC	1107
rs566758818	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7909139	CCCAACTCTGTGCCC[C/T]CAGCTCCTGGAGCAG	1107
rs566855005	snp	C/G			synonymous-codon	CHD3	GRCh38.p7	17:7899360	CCACACAAAAGGTCC[C/G]TTCCTGGTGAGTGCC	1107
rs566961362	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7887096	GGTAAAACTTCGGGA[A/T]ATTATTTTTAGCACA	1107
rs567051840	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886427	GCGGCACAAATGCAC[A/C]AAACTTCAAAACGGC	1107
rs567098669	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7910118	ACTCCCCGCCCCCAT[A/G]TCTTCCAATGTCCCC	1107
rs567394146	snp	G/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7889568	TTAATGCTTCCTAGA[G/T]AGTGGGAACTGCCGA	1107
rs567487765	snp	C/T	1.65411e-05	0.00287581	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903433	CTCCAAGGCAGGCTC[C/T]ATGTCCAAGCAGGAG	1107
rs567528323	snp	A/G	0.00142746	0.0266775	intron-variant, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902899	GTGGACAGAACTACC[A/G]GGTACAAGAAAAACC	1107
rs567588074	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884381	GAAATATTTCTGAGC[A/G]CCCCCCTCAGAATTT	1107
rs567605979	snp	G/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7894683	TGGTTTCACTTACCC[G/T]CTTCCTGCCCCCAGA	1107
rs567643418	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7887348	AAACGTTTAAAATAA[G/T]AGCAGTCGTGTTGGT	1107
rs567731285	snp	A/G	0.000798403	0.0199641	intron-variant	CHD3	GRCh38.p7	17:7894003	CAGGGATCCGTGAGG[A/G]CCAAGGATCCAGAGA	1107
rs568145842	snp	C/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904814	GAGATTTAAACTCTT[C/T]GGTGGTTGCACAGGC	1107
rs568271401	in-del	-/C	0.00636936	0.0560724	intron-variant	CHD3	GRCh38.p7	17:7896102	GCGTGGTGGCAGGCA[-/C]CTGTAGTCCCAGCTA	1107
rs568441362	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885203	CCGGAGCGCGAATCC[C/G]GGGCTCGGGCCCGTG	1107
rs568470967	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7887460	ATATAGATGTGATTC[A/C]TTGGGGGTGGGGGTG	1107
rs568530771	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888206	CCCCTGCACACACGC[A/C]CACAGTCCTAGAGTG	1107
rs568783199	snp	A/G/T	3.29746e-05	0.00406035	synonymous-codon, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906583	GTTCATGCGCCATCT[A/G/T]TGTGAGCCTGGGGCA	1107
rs568788886	snp	G/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905554	TCTTGTGGGAATGGG[G/T]TGCTAAGGAGGACTG	1107
rs568796599	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7894820	CACCAGTCTTCTCTG[C/T]ACTTCTAGGATTCAG	1107
rs568835948	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7897855	CAGCTCACTGTTGAC[A/G]GTTGGGTGACAAATT	1107
rs568900326	snp	A/C	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7902453	AATAAAAATAAGAAA[A/C]GAGAGTGTGACAAGA	1107
rs568913770	snp	A/C	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7901899	GGGAGGGTGAGCCAT[A/C]TGCCTCCTTAGGGAC	1107
rs568917982	snp	A/C	0.00119737	0.0244387	intron-variant	CHD3	GRCh38.p7	17:7901496	ATGAGGAGATTCCTC[A/C]TGTAAGAGTTTTTTT	1107
rs568976535	snp	A/G	0.00119737	0.0244387	intron-variant	CHD3	GRCh38.p7	17:7894028	CAGAGACAGGGATCC[A/G]TGAGGGATGGCGGAA	1107
rs569038974	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7909030	GGTTTGGAGCTGGGA[A/G]TGCCCTGGGCCAGCA	1107
rs569402679	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886223	TGACAAGTCACCCGG[C/G]GGCACTCTCTGGGCG	1107
rs569427804	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7899273	GGAAGATAAAGGGGT[A/G]TAGCTGGCAGAGGAC	1107
rs569535363	snp	C/T	1.65048e-05	0.00287265	missense	CHD3	GRCh38.p7	17:7898519	TTATGGGGGAAGACC[C/T]TGCCCAGCCCCGCAA	1107
rs569669003	snp	A/G	2.01595e-05	0.0031748	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890632	AGTCAGAGAGTGGGG[A/G]CAGTGAATATGGAAC	1107
rs569730060	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7891281	GCGAGGGGTGGAGGG[A/G]CCATCATGATTCCAG	1107
rs569985633	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7897837	TTCCAATCTCCCTTC[C/T]AGCAGCTCACTGTTG	1107
rs570033110	snp	A/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904909	GACTGAAGGTGGGCG[A/G/T]TGAATGGAGATGGTG	1107
rs570106053	snp	A/G	0.00159617	0.0282053	intron-variant	CHD3	GRCh38.p7	17:7890424	ACAGAGCAAGACTCC[A/G]TCTCCAAAAAAAAAA	1107
rs570133749	snp	A/G	0.000798403	0.0199641	intron-variant	CHD3	GRCh38.p7	17:7901177	CATCTGGCCTTCTAG[A/G]TGTGGCAAGAATATG	1107
rs570215686	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7896679	CAAAGTGCTGGGACG[C/T]GCCTGTTATTCTCTT	1107
rs570364541	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7911049	TGCTCAGCTGCCCTT[C/T]AACTGCTCTAGTCCA	1107
rs570455393	snp	C/T	0.00159617	0.0282053	intron-variant	CHD3	GRCh38.p7	17:7901631	TTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG	1107
rs570518871	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	CHD3, NAA38	GRCh38.p7	17:7883285	CACGGTACCTCAGTT[G/T]CTTCTACTTTATCGG	1107
rs570684756	snp	C/T			synonymous-codon	CHD3	GRCh38.p7	17:7908012	TATCGCCGATGGTGG[C/T]TTCACAGGTTGGGGA	1107
rs570818348	snp	A/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7891816	TAGTGAGCCGAGATC[A/T]CACCACTGCTATGCT	1107
rs570890656	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7891294	GGGCCATCATGATTC[C/T]AGTGCTGGGTTAGAG	1107
rs571014498	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905521	TCAAACGTGACAGGA[A/G]TGTTCCTGTGTTGTG	1107
rs571146266	snp	G/T	0.000138956	0.0083342	utr-variant-3-prime, synonymous-codon	CHD3	GRCh38.p7	17:7911653	AGCTCAAGCGCTGGG[G/T]CCTGCTGCCAGCCCT	1107
rs571205971	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904963	GACTTTGGGCAGTGA[G/T]CTGGTGTTCCCAGAA	1107
rs571267244	snp	C/T	0.000383573	0.0138434	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910894	GGGGTACGGGGCGGC[C/T]TTCAGCGCCGCACCC	1107
rs571296552	snp	C/T	0.00057305	0.0169173	intron-variant	CHD3	GRCh38.p7	17:7907538	GAATTTGGGATTTCC[C/T]TCTTCTGGGGTCAGG	1107
rs571437410	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7890369	GGGAGGTGGAGGTTG[C/T]AGTGAGCCGAGATCA	1107
rs571484803	snp	C/T	0.000798403	0.0199641	intron-variant	CHD3	GRCh38.p7	17:7896116	ACCTGTAGTCCCAGC[C/T]ACTCAGGAGGCTGAG	1107
rs571610027	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888627	GGGGCCTGGGGTCCT[C/T]TGGCAGAGACATCTG	1107
rs571634335	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7895595	CATTTCCTGCCATCC[C/T]CTCCCTCTCTTACTC	1107
rs571695525	snp	A/G	0.00159617	0.0282053	intron-variant	CHD3	GRCh38.p7	17:7897457	TTCCTCCAGGGGAAC[A/G]GGAGAAAACAGGAGG	1107
rs572038552	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7911257	AGTGAATATGAAACC[C/T]GAGGGGTTAGAGAGT	1107
rs572193528	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7903687	TTAAAACAAACAAAA[C/T]AAAAACCTTTCAACA	1107
rs572269936	snp	G/T	3.3557e-05	0.00409602	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903113	GCAAGGAGATGTGGG[G/T]TCATGGAGGAGGGTG	1107
rs572540707	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888553	CCTTTATGTGGGGTA[A/G]CTCTCCGTTCCGTTC	1107
rs572594107	snp	A/G	0.000148599	0.00861845	intron-variant	CHD3	GRCh38.p7	17:7890533	GTTTCTGGCAATGGT[A/G]GGGATGAATAAATGT	1107
rs572611695	snp	C/T	0.00159617	0.0282053	intron-variant	CHD3	GRCh38.p7	17:7895991	AGTACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA	1107
rs572653426	snp	G/T	6.70916e-05	0.00579148	intron-variant	CHD3	GRCh38.p7	17:7910347	CTGTATCTGTCCATC[G/T]GATGCCTCTCTTTTC	1107
rs572688412	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7909812	AAACTTCCCTTTGAC[C/T]TTCGACCTTTCCTCC	1107
rs572689252	in-del	-/T			intron-variant	CHD3	GRCh38.p7	17:7890445	AAAAAAAAAAGGAGA[-/T]TAAAAAATTAGTTAC	1107
rs572975258	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	CHD3	GRCh38.p7	17:7887786	TCCCTGAGATCCGAG[C/T]CGGGGATGTGGGAGA	1107
rs573142013	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7893679	CTGGAGGAGAGATGC[C/T]TTCCAGGAAGTGGGG	1107
rs573247120	snp	G/T	0.000742531	0.0192539	intron-variant	CHD3	GRCh38.p7	17:7900763	GCTGCCTGGAGTAGG[G/T]CTTGGGGATTGATGG	1107
rs573463606	in-del	-/G			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905255	TATACAAGTAAAAAA[-/G]TCTTCGTGTGTGTGT	1107
rs573962893	snp	A/G	4.9879e-05	0.0049937	intron-variant	CHD3	GRCh38.p7	17:7894111	GCCACGGGGCTATGG[A/G]CAGTATGTTTTTCAG	1107
rs573993812	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885267	GTGGCGGCTGCGACC[A/G]CGGGGCCAGGCCTCC	1107
rs574024772	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7887869	AGATTTGCTTTATTA[C/T]CCTTCCTTGCTTTTC	1107
rs574055948	snp	A/G	0.000399281	0.0141238	synonymous-codon	CHD3	GRCh38.p7	17:7909217	GTCGCAGGAGCCGGC[A/G]CACCCCGCCATGGCC	1107
rs574072575	snp	A/G	0.000798403	0.0199641	intron-variant	CHD3	GRCh38.p7	17:7908586	GATGATTTCACACCC[A/G]GGGACAGGGCTAGTG	1107
rs574327193	snp	C/G	0.167484	0.23599	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885746	AGACTTAGGTGCCCG[C/G]CAACTGAGGGGCATG	1107
rs574488138	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884289	TCTCCCTTTCTTTAT[A/G]GAGGGGGTGGCGGTG	1107
rs574601116	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7910834	TCCAACTTCTGCTTC[C/T]TCTCTGTTCCAGGCC	1107
rs574637512	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906070	CTTGGGGCCGCCATA[C/T]GATGTGACCTTACTC	1107
rs574676236	snp	C/T	6.59326e-05	0.00574125	missense	CHD3	GRCh38.p7	17:7906896	GAGCACATCAATGGG[C/T]GTTGGTCAATGCCGG	1107
rs574940576	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7892019	CCTCAATTTCCTCTT[C/T]TATAAACGGGGAATA	1107
rs575115295	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885921	AGTCCATTCGGATTG[C/G]GGAGCGGAGAGAAGA	1107
rs575352938	snp	G/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7892871	GATCATAGCTCACTA[G/T]ATCCTCCAACTCCTG	1107
rs575804930	snp	C/G/T	0.00159649	0.0282165	utr-variant-3-prime	CHD3	GRCh38.p7	17:7911936	CCTCCCCAGCCGTTT[C/G/T]CCTGCAGAATCAGCT	1107
rs575862839	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883506	GGAAAAGAGTAAAGA[A/T]AAAATTTATAACAAT	1107
rs575941947	snp	C/T	0	0	intron-variant	CHD3	GRCh38.p7	17:7911348	GTCTTCCCTCCCTCA[C/T]GTGGGACAACGGGAA	1107
rs575989571	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7891448	TGAACTTCCTTAGCT[C/T]ACTTAGCAGGTCCTG	1107
rs576018259	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7899274	GAAGATAAAGGGGTG[C/T]AGCTGGCAGAGGACT	1107
rs576061323	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7897480	ACAGGAGGAAAATCC[A/G]GCCAGGCAGTGCCTC	1107
rs576170265	snp	A/C	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7890024	GCAGCAAAGAGAAGC[A/C]GTTGAAAGCACAAGC	1107
rs576181084	snp	A/G/T	0.000380112	0.0137812	synonymous-codon	CHD3	GRCh38.p7	17:7893463	GTCAGCTGCTGTCTC[A/G/T]TCGGCCACCCCCATA	1107
rs576195479	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7895779	GCCTTTCCTAACTTC[A/G]TGTCCTTCCTTATCT	1107
rs576219563	in-del	-/GTT	0.0016691	0.0288403	intron-variant	CHD3	GRCh38.p7	17:7889991	CTAGTGAAGAGCCTC[-/GTT]GTCAGTGTGTCCTCA	1107
rs576445650	snp	A/C			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883612	CTATTCATATCTCTC[A/C]CCCAAAAGTCACTAG	1107
rs576579516	snp	C/T	1.64982e-05	0.00287208	missense	CHD3	GRCh38.p7	17:7899478	AGCCGGGCCATCATT[C/T]GTGAGAATGAATTCT	1107
rs576602592	snp	A/G	8.3273e-05	0.0064521	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906022	AGGGCTGAGTTGGAC[A/G]CAAGGGGAAGAGCTT	1107
rs576733984	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7892049	AATAATATATACCTC[A/G]TAGGAATCTGTGTGG	1107
rs576912264	snp	A/G	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7891493	GCCCTGGTAATAATG[A/G]AGGGTCCACTGCTGG	1107
rs577058113	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	CHD3	GRCh38.p7	17:7911974	ATGTGGAAGTGGAGA[A/C]TCAGCCTTGCCTGGC	1107
rs577075687	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912591	CCCAGGAGGGGCCGG[C/G]GAGAGTGGCAGTTTG	1107
rs577325529	snp	A/G	1.64746e-05	0.00287002	missense	CHD3	GRCh38.p7	17:7897176	GGCTCCGGCGAGGAT[A/G]ATGGGAAGAGCGACA	1107
rs577511736	snp	C/T	0.00318978	0.0398085	intron-variant	CHD3	GRCh38.p7	17:7896635	GTCTCGAACTCCCAA[C/T]CTCAGGTGATCCACC	1107
rs577686957	snp	C/T	1.76142e-05	0.00296762	intron-variant	CHD3	GRCh38.p7	17:7903778	TTTCCCATCAGCCTT[C/T]CTAAACTTTGGAACC	1107
rs577687053	snp	C/T	0.000399281	0.0141238	intron-variant	CHD3	GRCh38.p7	17:7911121	TTGTTCTAGGCTGTC[C/T]CCCCACCCATCCCTT	1107
rs577698773	snp	C/G	0.000798403	0.0199641	intron-variant	CHD3	GRCh38.p7	17:7910287	TTACTTTCTTGATCT[C/G]TGGTTCTTTGACATC	1107
rs578071288	snp	C/T	1.64836e-05	0.0028708	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903010	CAATCTGGCCACTGC[C/T]GACACTGTCATCATC	1107
rs578084733	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888489	GCTTGGTAGGGGAGG[A/G]ACGTGAACCAGAGCC	1107
rs578131103	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7896584	CTAATTTTGTATTTT[C/T]AGTAGAGACGGGGTT	1107
rs578139702	in-del	-/CTCT	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886105	ATTCACTGTCACTCA[-/CTCT]CTCGCTGAAACCACC	1107
rs745331215	snp	A/G			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905261	AGTAAAAAAGTCTTC[A/G]TGTGTGTGTGGAAAA	1107
rs745348749	snp	C/G	1.70319e-05	0.00291816	intron-variant	CHD3	GRCh38.p7	17:7894308	TGTCAGTGGGCCGTC[C/G]TCTCATTCTTATTTT	1107
rs745371861	snp	C/T	5.26413e-05	0.00513009	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906743	AGCTGGCTGCCTAGT[C/T]TCTGTCCTTCCTCTG	1107
rs745385380	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7891393	CTTCTGCTCTGTGAC[G/T]TCTCTCTAGACTGGA	1107
rs745416944	snp	C/G	1.65315e-05	0.00287498	intron-variant	CHD3	GRCh38.p7	17:7907269	GGCTCCCTGGATTCC[C/G]CTGTGGAGCGGGAGG	1107
rs745437593	snp	A/G	1.64765e-05	0.00287019	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890957	AGTGGAACAGAAGTC[A/G]TCAGCAACTCTGCTT	1107
rs745452588	snp	A/C	0.000231696	0.0107608	intron-variant	CHD3	GRCh38.p7	17:7897301	CAACCACAGGTGAAT[A/C]CTCGGTCCCTGGGAA	1107
rs745538295	snp	A/G	3.30655e-05	0.00406591	synonymous-codon	CHD3	GRCh38.p7	17:7894231	CCGCACCAAGAAACT[A/G]AAGAGAGGCCGGCCA	1107
rs745547262	snp	C/G	0.0268207	0.112654	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905955	ACACAGTGGCTGGTG[C/G]GGGACCTGAGGGGCA	1107
rs745605763	snp	A/C	3.22066e-05	0.00401276	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911678	AGCCCTCCACCTTCC[A/C]CACCCCTTGGGCCAT	1107
rs745605845	snp	A/G	0.00011753	0.00766492	intron-variant	CHD3	GRCh38.p7	17:7909100	AGCCCCTCACCCACT[A/G]CTGGCAGAGCCCTAC	1107
rs745637501	snp	A/G	3.29527e-05	0.00405898	missense	CHD3	GRCh38.p7	17:7903905	GACCGGAACCAGGAT[A/G]CAACTGAGGACACTG	1107
rs745703255	snp	C/T	1.64735e-05	0.00286993	intron-variant, missense	CHD3	GRCh38.p7	17:7889071	GGATTTCTTTTCCTC[C/T]AGGACTGTGTTGGGG	1107
rs745706384	snp	A/C	1.75919e-05	0.00296574	intron-variant	CHD3	GRCh38.p7	17:7903784	ATCAGCCTTTCTAAA[A/C]TTTGGAACCCAAAGT	1107
rs745707523	snp	C/T	1.64852e-05	0.00287094	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906575	GTGTCTTTGTTCATG[C/T]GCCATCTGTGTGAGC	1107
rs745803889	snp	A/G	0.000125589	0.00792329	synonymous-codon	CHD3	GRCh38.p7	17:7909292	CCAGCACCTCTCCAA[A/G]GAGTCGCTGGCGGGG	1107
rs745813551	snp	A/C	0.00164451	0.0286278	synonymous-codon	CHD3	GRCh38.p7	17:7893505	ACCCCCCGCCCTTCC[A/C]CCACCCCCTGCTGCT	1107
rs745829732	snp	C/T	4.94458e-05	0.00497197	synonymous-codon	CHD3	GRCh38.p7	17:7895106	TGTCTAAACCCTCCC[C/T]TGCCTGACATTCCCA	1107
rs745890382	in-del	-/TTT	1.67621e-05	0.00289495	intron-variant	CHD3	GRCh38.p7	17:7895160	GCACAGTGAGTGGAA[-/TTT]ACATCTCCCCTCTGT	1107
rs745908039	snp	A/G	0.000189454	0.00973093	intron-variant	CHD3	GRCh38.p7	17:7889805	ATTCCTAACTCTGTG[A/G]CAAGGCTCAAGAGAC	1107
rs745917719	snp	A/T			intron-variant	CHD3	GRCh38.p7	17:7890226	ATTTGAGGTCAGGAG[A/T]TCGCGACAAGCCTGG	1107
rs745925634	snp	C/T	1.74455e-05	0.00295338	intron-variant	CHD3	GRCh38.p7	17:7901221	AACTGACCCCCTCCT[C/T]CTCCTCTCTCCTCCC	1107
rs745968236	in-del	-/C	0.000371604	0.0136258	frameshift-variant	CHD3	GRCh38.p7	17:7893490	ATAGCACCCTCCGGA[-/C]CCCCCCGCCCTTCCA	1107
rs745992945	snp	C/T	2.07295e-05	0.00321936	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890610	GAGCGAGATGAGTAC[C/T]GGGAGAAGTCAGAGA	1107
rs746005179	snp	G/T	1.6476e-05	0.00287014	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904519	GAAGCTGCTGAGGCA[G/T]CACTATGAGCAACAG	1107
rs746006633	snp	A/C	3.35177e-05	0.00409362	intron-variant	CHD3	GRCh38.p7	17:7898995	CCTTGAGCTTTCTGA[A/C]TTCTTGTCTCTATAG	1107
rs746076075	snp	A/G	1.83454e-05	0.00302859	intron-variant	CHD3	GRCh38.p7	17:7907531	GGGATTAGAATTTGG[A/G]ATTTCCCTCTTCTGG	1107
rs746087583	snp	A/G	5.03977e-05	0.00501959	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910588	GGAGCCTCACCCCAC[A/G]CCGGTAACCCTCTTT	1107
rs746088225	snp	A/C			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7887520	CTGGTAGTTTCTTTG[A/C]AAAAGGTCTGAAAAT	1107
rs746098127	snp	C/T	1.71021e-05	0.00292416	synonymous-codon	CHD3	GRCh38.p7	17:7901369	CCGAGTGCTCATCTT[C/T]TCGCAGGTGACCTGT	1107
rs746154367	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7909076	GTCTCTTGCTATGTC[C/T]GCCCCCCCAGCCCCT	1107
rs746170678	snp	C/T	2.80344e-05	0.00374385	intron-variant	CHD3	GRCh38.p7	17:7908376	CAAAACCCTGTTACC[C/T]CTTCTGTCTGCTGCC	1107
rs746192275	snp	A/G	1.64743e-05	0.00287	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895401	GGGGGAGCCACCTGT[A/G]GCAGTGCCAGCCCCT	1107
rs746195904	snp	C/T			intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906435	GCCCAGGGGAGGAGC[C/T]CTGGAGCACCTGGGG	1107
rs746207754	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7895251	TTCTCTGCACTCCCC[C/T]ACCCTTGTGGGACCC	1107
rs746209282	snp	C/T	0.00011816	0.00768546	intron-variant	CHD3	GRCh38.p7	17:7899566	CCTCTACCTCATATC[C/T]TCTGAGACCCTCAAA	1107
rs746235212	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7896725	GTGCAGTGGTGTGAT[A/C]TTGGCTCGCTGCAAC	1107
rs746299261	snp	A/T	1.67335e-05	0.00289248	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903104	CACCATTTAGCAAGG[A/T]GATGTGGGTTCATGG	1107
rs746307733	snp	A/G	1.64743e-05	0.00287	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895500	CTTTGTCAAGTGGGT[A/G]GGACTATCCTACTGG	1107
rs746347255	snp	C/G	0.000197847	0.00994406	missense, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902939	TCTCACCTCCTAGCT[C/G]CTGGGGCCCAACAAT	1107
rs746366053	snp	A/T	8.30668e-05	0.00644411	intron-variant	CHD3	GRCh38.p7	17:7891107	AATTGACACTTTTAA[A/T]TTGAGGGAGGTCCTG	1107
rs746403525	snp	C/T	3.29549e-05	0.00405911	synonymous-codon	CHD3	GRCh38.p7	17:7899955	GCTGATCACCATTGA[C/T]CAGGCAGCACTTGGT	1107
rs746428443	in-del	-/TTGGGGA	3.30237e-05	0.00406335	intron-variant	CHD3	GRCh38.p7	17:7900765	TGCCTGGAGTAGGGC[-/TTGGGGA]TTGATGGGAGCGTTC	1107
rs746451017	in-del	-/TT			downstream-variant-500B	CHD3, LOC284023	GRCh38.p7	17:7913169	GAAGCAAAGGCACAC[-/TT]TTTTTTTTTTTTTTT	1107
rs746462560	snp	A/G	1.69651e-05	0.00291243	intron-variant	CHD3	GRCh38.p7	17:7910982	ATCACAGGTCAGCTG[A/G]TGTTTTCCTACCCCC	1107
rs746466089	snp	A/G	1.6766e-05	0.00289529	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903108	ATTTAGCAAGGAGAT[A/G]TGGGTTCATGGAGGA	1107
rs746507064	in-del	-/CAACGGCCCTCCA	1.64819e-05	0.00287066	frameshift-variant	CHD3	GRCh38.p7	17:7911471	CCAAACAGCCGCCAC[-/CAACGGCCCTCCA]GTGCTTGTGAAGAAG	1107
rs746550117	snp	A/C	3.31175e-05	0.00406911	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905988	ACTGAGAAGGAGTTT[A/C]AGTGAGTGTGGGTGA	1107
rs746654254	snp	C/T	3.33272e-05	0.00408197	synonymous-codon	CHD3	GRCh38.p7	17:7894437	CTGTCCTGCAGTGGC[C/T]GGGGAGGAGGAGGTT	1107
rs746749703	snp	C/G	0.000264616	0.0114995	intron-variant	CHD3	GRCh38.p7	17:7907280	TTCCCCTGTGGAGCG[C/G]GAGGGGAGGGGGCTT	1107
rs746769482	snp	G/T	1.64749e-05	0.00287005	missense	CHD3	GRCh38.p7	17:7900904	GCCTTGAATTCACGA[G/T]GTGGTGGGAACCAGG	1107
rs746773769	snp	A/G	4.02309e-05	0.00448485	intron-variant	CHD3	GRCh38.p7	17:7889629	GAGGCTGGAAACCTA[A/G]AGGCTTAGGTTTTCT	1107
rs746837629	snp	C/G/T	0.000129274	0.00803868	synonymous-codon	CHD3	GRCh38.p7	17:7909319	GGGGAACAAGCCGGC[C/G/T]AACGCCGTCCTGCAC	1107
rs746838409	snp	A/G	1.64974e-05	0.00287201	intron-variant	CHD3	GRCh38.p7	17:7900737	CCATGCAGAAGTAAG[A/G]TGCAAGACGAGCTGC	1107
rs746854762	snp	C/G	1.65446e-05	0.00287612	missense	CHD3	GRCh38.p7	17:7898500	TCTTTTTCCAGAGAA[C/G]TAATTATGGGGGAAG	1107
rs746861469	snp	A/C	3.81134e-05	0.00436523	intron-variant	CHD3	GRCh38.p7	17:7904094	TGTCCCCCTTAAAAC[A/C]GTAGTGGACCTCAAA	1107
rs746886466	snp	C/T	1.72555e-05	0.00293725	intron-variant	CHD3	GRCh38.p7	17:7894378	CTCCATCTCCCCCTG[C/T]CCTGCTTCCTTATCC	1107
rs746946162	snp	A/C	1.70983e-05	0.00292384	intron-variant	CHD3	GRCh38.p7	17:7907350	CCCATTGTCCTCTTC[A/C]AGGCTGATGCCCCCA	1107
rs746970749	snp	A/G	4.94539e-05	0.00497238	missense	CHD3	GRCh38.p7	17:7893823	CAGGCCATAAGAGGC[A/G]GAGTAAGAGCCCCCG	1107
rs746991015	snp	G/T	1.66136e-05	0.00288211	intron-variant	CHD3	GRCh38.p7	17:7898122	GGGAATGAGCTTGTG[G/T]ATTCAAGGGATTCTG	1107
rs746996390	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7889205	CACCTTTGGCTCTCC[C/T]TCCCCAGCATCTGGC	1107
rs747051285	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7890035	AAGCAGTTGAAAGCA[C/T]AAGCTCTGGAAGACT	1107
rs747064258	snp	A/G	3.29544e-05	0.00405908	missense	CHD3	GRCh38.p7	17:7902665	ATGAAGGCTACAAGT[A/G]TGAGCGCATCGATGG	1107
rs747083149	snp	C/T	9.98369e-05	0.00706459	synonymous-codon	CHD3	GRCh38.p7	17:7899016	GTCTCTATAGCCTAC[C/T]GTGAAATATGAGACT	1107
rs747086994	snp	C/T	3.46789e-05	0.00416392	intron-variant	CHD3	GRCh38.p7	17:7894880	TTCATTCCTTAATTT[C/T]TTCCATCTGTCTGTG	1107
rs747105273	in-del	-/A	0.000117062	0.00764965	intron-variant	CHD3	GRCh38.p7	17:7901018	CAGAGCAGGGAGCTG[-/A]TCGAACGCCCATTCT	1107
rs747150252	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905113	AGACAACCAGTCAGA[A/G]TACTCGGTGGGTTCA	1107
rs747220628	snp	C/T	1.64811e-05	0.00287059	synonymous-codon	CHD3	GRCh38.p7	17:7899184	AACCATCGTCTTCCT[C/T]TACTCACTCTACAAG	1107
rs747229310	snp	C/G	3.44139e-05	0.00414799	intron-variant	CHD3	GRCh38.p7	17:7907728	GAAGGGACCGGACAC[C/G]TGGGTCCCAGAGGGC	1107
rs747237620	snp	A/G	0.000108501	0.0073647	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906209	GGCATCCTCCCCAGG[A/G]GAGGGGCGTTGAAGC	1107
rs747258702	snp	A/G	2.01339e-05	0.00317278	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890631	AAGTCAGAGAGTGGG[A/G]GCAGTGAATATGGAA	1107
rs747278665	snp	A/G	1.64906e-05	0.00287142	intron-variant	CHD3	GRCh38.p7	17:7911414	TTGTCATGAAGTGAC[A/G]TTTGAGAGTGATCTG	1107
rs747288057	snp	C/T	6.61583e-05	0.00575107	intron-variant	CHD3	GRCh38.p7	17:7907049	AATCAGAAGTCAGGA[C/T]GGTGGGAGAGACAGA	1107
rs747299117	in-del	-/C	0.00090691	0.0212752	frameshift-variant, intron-variant	CHD3	GRCh38.p7	17:7895446	AATCCAGATGTCCCA[-/C]CCCCCCCGTCCTCTT	1107
rs747304332	snp	C/G	1.73622e-05	0.00294632	intron-variant	CHD3	GRCh38.p7	17:7893970	CTACTAAACACCTGG[C/G]GGCCAAGGATCCAGA	1107
rs747373716	snp	A/G	1.6736e-05	0.0028927	intron-variant	CHD3	GRCh38.p7	17:7908557	GGTTCTCTCAAGCTG[A/G]CAAAAAAAAAAAAGA	1107
rs747387897	snp	A/T	3.60939e-05	0.00424802	intron-variant	CHD3	GRCh38.p7	17:7889817	GTGGCAAGGCTCAAG[A/T]GACCCATTCTCAGAG	1107
rs747440932	snp	C/T	1.6492e-05	0.00287154	missense	CHD3	GRCh38.p7	17:7906939	ACCCCAGCGCCGATT[C/T]TAAGCGCTCCTCCAG	1107
rs747446011	snp	A/G	3.37331e-05	0.00410675	synonymous-codon	CHD3	GRCh38.p7	17:7900027	ACTCAAGAACAACCA[A/G]TCCAAGGTGAGTGAG	1107
rs747457869	snp	C/T	3.31027e-05	0.0040682	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910507	GCTGTCCCGAATACC[C/T]CCCATCGCAGCCCGC	1107
rs747464671	snp	A/G	1.66496e-05	0.00288522	intron-variant	CHD3	GRCh38.p7	17:7894107	GACGGCCACGGGGCT[A/G]TGGGCAGTATGTTTT	1107
rs747520693	snp	A/G	1.64779e-05	0.00287031	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905049	AAGGGCCTCAGCATG[A/G]GCATATCCCGAGAGC	1107
rs747539733	snp	C/T	3.33233e-05	0.00408173	intron-variant	CHD3	GRCh38.p7	17:7895570	TTTCTTTCCCTCTCC[C/T]CCATGACCTCATTTC	1107
rs747550371	snp	G/T	1.64746e-05	0.00287002	missense	CHD3	GRCh38.p7	17:7897158	CCCCCACCCCTGGAC[G/T]ATGGCTCCGGCGAGG	1107
rs747582162	snp	A/G	8.85983e-05	0.00665517	intron-variant	CHD3	GRCh38.p7	17:7900056	AGGTTTCCAGACCTA[A/G]AAAACTTGAAGTTGT	1107
rs747588623	snp	A/G	5.04418e-05	0.00502179	intron-variant	CHD3	GRCh38.p7	17:7895588	ATGACCTCATTTCCT[A/G]CCATCCTCTCCCTCT	1107
rs747601165	snp	C/G	1.64895e-05	0.00287132	intron-variant	CHD3	GRCh38.p7	17:7908671	CCTGTTAAATTCCTT[C/G]ATGGTTCCTTTTCCT	1107
rs747614242	snp	A/T			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883904	AGAAAATAAAAAAAA[A/T]TAAATCTAGTTGGAC	1107
rs747622829	snp	C/T	3.94112e-05	0.00443892	intron-variant	CHD3	GRCh38.p7	17:7903541	TGTGAAAGCAGGCCC[C/T]TGCTCTCTCAGGAGT	1107
rs747634965	in-del	-/AAAT			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7887622	GGGGAATTTGAGAAA[-/AAAT]AAATATATGTGTGAG	1107
rs747639418	snp	A/G	4.94507e-05	0.00497221	missense, synonymous-codon	CHD3	GRCh38.p7	17:7911476	CAGCCGCCACCAACG[A/G]CCCTCCAGTGCTTGT	1107
rs747681715	in-del	-/T			downstream-variant-500B	CHD3, LOC284023	GRCh38.p7	17:7913170	AAGCAAAGGCACACT[-/T]TTTTTTTTTTTTTTT	1107
rs747697924	snp	A/G	0.000132092	0.00812579	intron-variant, utr-variant-5-prime	CHD3	GRCh38.p7	17:7888961	TAGGCTACTTGGGAG[A/G]AGGAATATTTAGGTA	1107
rs747768901	snp	A/G	1.64746e-05	0.00287002	missense	CHD3	GRCh38.p7	17:7897167	CTGGACTATGGCTCC[A/G]GCGAGGATGATGGGA	1107
rs747800972	snp	A/G	1.65329e-05	0.0028751	intron-variant	CHD3	GRCh38.p7	17:7907058	TCAGGATGGTGGGAG[A/G]GACAGAAAGGGAGCC	1107
rs747811663	in-del	-/AAAAT			intron-variant	CHD3	GRCh38.p7	17:7902442	AAATAAAAATAAATA[-/AAAAT]AAGAAAAGAGAGTGT	1107
rs747819036	snp	C/T			synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905691	ACTGCTGGCCCGAGT[C/T]GGGGGCAACATTGAG	1107
rs747871940	in-del	-/CGT			intron-variant	CHD3	GRCh38.p7	17:7901214	GTTTCCAACTGACCC[-/CGT]CCTCCTCCTCCTCTC	1107
rs747893936	snp	A/G	1.66158e-05	0.0028823	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906014	GGTGATACAGGGCTG[A/G]GTTGGACGCAAGGGG	1107
rs747932461	snp	A/C	3.30028e-05	0.00406205	missense	CHD3	GRCh38.p7	17:7898524	GGGGAAGACCCTGCC[A/C]AGCCCCGCAAGTATA	1107
rs747936150	snp	C/T	1.71457e-05	0.0029279	missense	CHD3	GRCh38.p7	17:7907368	GCTGATGCCCCCAGC[C/T]CAGCCCCATCACTTG	1107
rs747936810	snp	C/G			intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903177	GGAGGAGAGAAGGCC[C/G]TTCTTCAGCAGCCTT	1107
rs747946918	snp	A/G	1.65987e-05	0.00288082	missense	CHD3	GRCh38.p7	17:7894441	CCTGCAGTGGCCGGG[A/G]AGGAGGAGGTTGATG	1107
rs747954298	snp	A/G	1.74653e-05	0.00295505	intron-variant	CHD3	GRCh38.p7	17:7894654	CTGAGGAACCCACCC[A/G]TCTCTTTCCCCCTTG	1107
rs748034906	snp	C/T	1.82061e-05	0.00301708	synonymous-codon	CHD3	GRCh38.p7	17:7893295	TTACAGGCCCCTAAT[C/T]GCTAAGAAGAATCCT	1107
rs748086572	snp	C/G	1.69579e-05	0.00291182	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906106	ATTATCACCCTCCCT[C/G]TCATACAATACTTCC	1107
rs748114581	snp	A/G	2.68547e-05	0.00366423	intron-variant	CHD3	GRCh38.p7	17:7889788	GCGTGTAAGTGTCAA[A/G]AATTCCTAACTCTGT	1107
rs748195247	snp	C/G	1.68105e-05	0.00289914	intron-variant	CHD3	GRCh38.p7	17:7895165	AGTGAGTGGAAACAT[C/G]TCCCCTCTGTATTTA	1107
rs748203257	snp	C/T	1.65285e-05	0.00287471	intron-variant	CHD3	GRCh38.p7	17:7899309	TATACGGCCTCTAGC[C/T]TAGACTTATGCTGCC	1107
rs748229722	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7897576	GCATGAAAGCAAAAC[A/C]TGAGAGACATAATTC	1107
rs748236185	snp	A/T	3.32353e-05	0.00407634	intron-variant	CHD3	GRCh38.p7	17:7893756	CTCCATAATTCCAGG[A/T]TGTCATGACCTCTCC	1107
rs748293338	snp	G/T	1.64955e-05	0.00287184	intron-variant	CHD3	GRCh38.p7	17:7899209	TACAAGGAGGTGCTG[G/T]ATTCTAGGACCTTGA	1107
rs748298491	snp	C/G	7.11415e-05	0.0059637	intron-variant	CHD3	GRCh38.p7	17:7907863	AGGAGGGTGTCCTGA[C/G]GTGTGAGCTTTGACC	1107
rs748325173	snp	C/T	1.64969e-05	0.00287196	intron-variant, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902931	GATCCAACTCTCACC[C/T]CCTAGCTCCTGGGGC	1107
rs748336023	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7896140	GGCTGAGACAGGAGA[A/G]TGGCGTGAACCCGGG	1107
rs748391145	snp	C/T	1.6476e-05	0.00287014	missense	CHD3	GRCh38.p7	17:7895025	CACATGGAGTACTGC[C/T]GCGTATGCAAGGACG	1107
rs748391954	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7910623	CTAGCTCCAGTTTTC[C/T]CTGTTTGTGTTCCTC	1107
rs748424391	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905131	CTCGGTGGGTTCAGA[A/G]GAGGAGGATGAAGAC	1107
rs748425817	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7898909	CAGGCCATAGTAGAG[A/G]GAATTGTAATCCAAC	1107
rs748466322	in-del	-/TTGA	1.90958e-05	0.00308991	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906262	TAGCCTCACATTTAC[-/TTGA]TTGACCACAATAACC	1107
rs748472194	in-del	-/GCA	0.0163923	0.0890362	cds-indel	CHD3	GRCh38.p7	17:7893416	GTGGCGGCGGCAGCG[-/GCA]GCAGCAGCAGCAGCT	1107
rs748486028	snp	C/T	1.65135e-05	0.00287341	synonymous-codon	CHD3	GRCh38.p7	17:7894210	AGGCCGGCCTGATGG[C/T]CCTGTCCGCACCAAG	1107
rs748527163	in-del	-/GAGGAGGAAGAA	0.000240703	0.0109678	cds-indel, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884861	GAGATGGTGGTGTCG[-/GAGGAGGAAGAA]GAGGAGGAAGAAGAG	1107
rs748572297	snp	G/T	2.47749e-05	0.00351949	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890717	AAAGCGGCGGAAAAA[G/T]GGGGAGGGAGATGGG	1107
rs748576169	snp	A/G	1.64841e-05	0.00287085	missense	CHD3	GRCh38.p7	17:7907149	GCTCCAAGTGAGAAA[A/G]GAGAAGGCATAAGGA	1107
rs748588194	snp	A/G	4.92647e-05	0.00496286	missense, intron-variant	CHD3	GRCh38.p7	17:7907630	CCAGGAGAAAGGGGG[A/G]AGGAGAAGCCGTTGG	1107
rs748618377	snp	A/G	4.94458e-05	0.00497197	synonymous-codon	CHD3	GRCh38.p7	17:7902690	CGATGGTGGTATCAC[A/G]GGTGCCCTGAGGCAG	1107
rs748640394	snp	C/T	1.65963e-05	0.0028806	intron-variant	CHD3	GRCh38.p7	17:7910839	CTTCTGCTTCCTCTC[C/T]GTTCCAGGCCTACCC	1107
rs748713277	snp	C/T	0.000115425	0.00759599	intron-variant	CHD3	GRCh38.p7	17:7907118	TATCACTGTGCCTTC[C/T]CCTGCAGCTACTCCA	1107
rs748722809	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	CHD3	GRCh38.p7	17:7897175	TGGCTCCGGCGAGGA[C/T]GATGGGAAGAGCGAC	1107
rs748755876	snp	A/G	3.29685e-05	0.00405995	synonymous-codon	CHD3	GRCh38.p7	17:7907163	AGGAGAAGGCATAAG[A/G]ACACCTCTTGAGAAG	1107
rs748769546	snp	C/G	1.64822e-05	0.00287068	missense	CHD3	GRCh38.p7	17:7900604	GACATATCCAAAGAG[C/G]ACCAGATCAAGAAAC	1107
rs748794182	snp	C/T	4.99446e-05	0.00499698	intron-variant	CHD3	GRCh38.p7	17:7908864	GGAGCGGGTTATAGA[C/T]GGGCTTGGGTCAGAA	1107
rs748814939	snp	A/C/G	3.2955e-05	0.00405914	synonymous-codon	CHD3	GRCh38.p7	17:7903883	TGAGGCCATCGCTCG[A/C/G]CTGTTGGACCGGAAC	1107
rs748859552	snp	A/C	1.64874e-05	0.00287113	synonymous-codon	CHD3	GRCh38.p7	17:7900382	GGAGCTCTTCCATCT[A/C]CTGAACTTCCTCACC	1107
rs748896554	snp	C/T	4.94385e-05	0.0049716	intron-variant, utr-variant-5-prime	CHD3	GRCh38.p7	17:7888993	TTGTGGAGACTTTCT[C/T]CTGTGTGATGAAGGC	1107
rs748950223	snp	A/G	6.6048e-05	0.00574627	synonymous-codon	CHD3	GRCh38.p7	17:7907247	GAAGATGGAGACAGA[A/G]GTGTGTGGCTCCCTG	1107
rs748967512	snp	C/T	1.64955e-05	0.00287184	missense	CHD3	GRCh38.p7	17:7897275	GAGTGGATGACCGTC[C/T]ACCGCATCATCAACC	1107
rs748998349	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7890229	TGAGGTCAGGAGTTC[A/G]CGACAAGCCTGGCCA	1107
rs749042862	snp	A/C/G	6.59287e-05	0.00574113	synonymous-codon, missense	CHD3	GRCh38.p7	17:7911483	CACCAACGGCCCTCC[A/C/G]GTGCTTGTGAAGAAG	1107
rs749046452	in-del	-/ATCT	1.68275e-05	0.0029006	intron-variant	CHD3	GRCh38.p7	17:7910343	TGCCTGTATCTGTCC[-/ATCT]ATCTGATGCCTCTCT	1107
rs749054568	snp	A/G	0.000120202	0.00775155	synonymous-codon	CHD3	GRCh38.p7	17:7893466	AGCTGCTGTCTCGTC[A/G]GCCACCCCCATAGCA	1107
rs749067417	snp	A/G	1.78844e-05	0.0029903	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906193	TAGAGTAGAGGGGCC[A/G]GGCATCCTCCCCAGG	1107
rs749083605	snp	A/G	5.10547e-05	0.0050522	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906114	CCTCCCTGTCATACA[A/G]TACTTCCTGGCTCGA	1107
rs749096335	in-del	-/C	4.18524e-05	0.00457432	intron-variant	CHD3	GRCh38.p7	17:7907588	CCTTCCTATCCCCTA[-/C]CCCCTCCCACAGCCA	1107
rs749147376	snp	C/G	4.84179e-05	0.00492002	missense, intron-variant	CHD3	GRCh38.p7	17:7907621	GAGTCGACGCCAGGA[C/G]AAAGGGGGGAGGAGA	1107
rs749149678	snp	C/T	0.0102656	0.0709043	missense	CHD3	GRCh38.p7	17:7893501	CCGGACCCCCCGCCC[C/T]TCCACCACCCCCTGC	1107
rs749158256	snp	G/T	2.5665e-05	0.00358216	missense, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884853	AGGAGGAGGAGATGG[G/T]GGTGTCGGAGGAGGA	1107
rs749172317	snp	C/T	1.654e-05	0.00287571	synonymous-codon, stop-gained	CHD3	GRCh38.p7	17:7911579	GGTGATCTGTATAGA[C/T]GACTGACTGGATCCC	1107
rs749255431	snp	G/T	1.7357e-05	0.00294588	intron-variant	CHD3	GRCh38.p7	17:7894866	CTGTATCTTCCAGTT[G/T]CATTCCTTAATTTCT	1107
rs749266184	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7889549	GAGGCAGGGCTTGGA[A/G]GAGTTAATGCTTCCT	1107
rs749283113	snp	A/G	3.29701e-05	0.00406005	missense	CHD3	GRCh38.p7	17:7906897	AGCACATCAATGGGC[A/G]TTGGTCAATGCCGGA	1107
rs749330456	snp	A/G	1.64781e-05	0.00287033	missense	CHD3	GRCh38.p7	17:7893838	GGAGTAAGAGCCCCC[A/G]AGTGCCTGATGGACG	1107
rs749377815	snp	C/T	2.95225e-05	0.00384192	intron-variant	CHD3	GRCh38.p7	17:7889654	TTTTCTGATGCTTTT[C/T]GCTTCAAAGATAAGG	1107
rs749421338	snp	A/G	6.58892e-05	0.00573936	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905107	CCCCACAGACAACCA[A/G]TCAGAGTACTCGGTG	1107
rs749439309	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7890792	CATTAAAGACGGGCA[C/T]GAGGAGGGGAGGAAT	1107
rs749455615	snp	C/G	1.7025e-05	0.00291757	intron-variant	CHD3	GRCh38.p7	17:7910334	GCTCTTTTTCTGCCT[C/G]TATCTGTCCATCTGA	1107
rs749482090	snp	C/T	1.67916e-05	0.0028975	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904429	AGTGTTCATTCATTC[C/T]GTTGCCCTTCAGATT	1107
rs749526156	snp	C/T	1.65787e-05	0.00287907	intron-variant	CHD3	GRCh38.p7	17:7893776	ATGACCTCTCCTTTT[C/T]CCTCTTCTCACCCCG	1107
rs749528280	snp	G/T	1.64749e-05	0.00287005	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895389	ACATTGGCGGTGGGG[G/T]GAGCCACCTGTAGCA	1107
rs749533759	snp	A/G	1.6476e-05	0.00287014	synonymous-codon	CHD3	GRCh38.p7	17:7900927	GAACCAGGTGTCGCT[A/G]CTTAATATCATGATG	1107
rs749584438	snp	A/G	1.64817e-05	0.00287064	synonymous-codon, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902950	AGCTCCTGGGGCCCA[A/G]CAATTCTGCTTCCTC	1107
rs749592108	snp	A/G			intron-variant, upstream-variant-2KB, utr-variant-5-prime	CHD3, NAA38	GRCh38.p7	17:7886899	TGGGTCTTTGTGTCA[A/G]CCCGGCCTCCCCTTT	1107
rs749619595	snp	A/T			intron-variant	CHD3	GRCh38.p7	17:7908922	GGAAGGTTAACACCT[A/T]CAGGGCTGAGGTGAT	1107
rs749680912	in-del	-/GAA	1.65181e-05	0.00287381	cds-indel	CHD3	GRCh38.p7	17:7894950	TGGGAGGCCAAGGAG[-/GAA]GAAGAAGAATACGAA	1107
rs749681638	snp	C/T	1.65941e-05	0.00288041	missense	CHD3	GRCh38.p7	17:7910853	CTGTTCCAGGCCTAC[C/T]CGCCGGGTCCCTACG	1107
rs749717891	snp	C/T	1.65759e-05	0.00287883	intron-variant	CHD3	GRCh38.p7	17:7902740	ATGGTGAGGGAGATA[C/T]ACTGGTCCCTGGTGG	1107
rs749722273	snp	A/T	3.427e-05	0.00413931	intron-variant	CHD3	GRCh38.p7	17:7895199	TCAGGCCTGATCCCT[A/T]CCCCCATCCCTGGGG	1107
rs749724796	snp	A/G	3.90282e-05	0.0044173	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905692	CTGCTGGCCCGAGTC[A/G]GGGGCAACATTGAGG	1107
rs749734103	snp	A/G	1.65474e-05	0.00287636	missense	CHD3	GRCh38.p7	17:7899506	TCTCCTTTGAGGACA[A/G]TGCCATCAAAGGGGG	1107
rs749780557	snp	C/T	8.26003e-05	0.00642599	intron-variant	CHD3	GRCh38.p7	17:7899324	CTAGACTTATGCTGC[C/T]CCCATTCTTGACTCC	1107
rs749795882	snp	A/G	1.67683e-05	0.00289549	missense	CHD3	GRCh38.p7	17:7907996	CCCGGTTCATGTTCA[A/G]TATCGCCGATGGTGG	1107
rs749820941	snp	A/G	2.42816e-05	0.00348428	intron-variant	CHD3	GRCh38.p7	17:7890751	CAAAAGGTGAGTAGA[A/G]TTAGGGAATGAGAGT	1107
rs749869917	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7894737	TGTCCGAGTGTCTAG[G/T]ATCCTAATGTATTCC	1107
rs749874030	in-del	-/ATAGCA	0.000117103	0.007651	cds-indel	CHD3	GRCh38.p7	17:7893476	TCGTCGGCCACCCCC[-/ATAGCA]CCCTCCGGACCCCCC	1107
rs749875840	snp	G/T			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886524	TAGCCGAGACGACCT[G/T]TGGGGGAGCGGGGGG	1107
rs749879125	snp	C/T			intron-variant, utr-variant-5-prime	CHD3	GRCh38.p7	17:7888954	TAGGTTTTAGGCTAC[C/T]TGGGAGGAGGAATAT	1107
rs749885293	snp	C/G	1.65176e-05	0.00287376	intron-variant	CHD3	GRCh38.p7	17:7910423	CTCTGTGGCCCGGGC[C/G]CCAGTTCTGAACCAG	1107
rs749927725	snp	A/G	5.03031e-05	0.00501488	intron-variant	CHD3	GRCh38.p7	17:7901021	AGCAGGGAGCTGATC[A/G]AACGCCCATTCTCAG	1107
rs749962619	in-del	-/AGA	6.7954e-05	0.00582858	cds-indel	CHD3	GRCh38.p7	17:7890692	ACCGAGAAAAAAAGG[-/AGA]AGAAGACAAAGCGGC	1107
rs749985512	snp	C/T	8.84025e-05	0.00664781	intron-variant	CHD3	GRCh38.p7	17:7910314	CATCTGTGTTCTCCT[C/T]TCTCGCTCTTTTTCT	1107
rs749991702	snp	A/G	1.69913e-05	0.00291468	intron-variant	CHD3	GRCh38.p7	17:7894406	TCCCTCCACCGGGGT[A/G]TATGACAGTCCTGGG	1107
rs750017568	snp	C/G	1.70041e-05	0.00291577	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904411	GCAAAGAAGGAGACC[C/G]CCAGTGTTCATTCAT	1107
rs750022126	snp	C/T	1.89881e-05	0.00308119	intron-variant	CHD3	GRCh38.p7	17:7898621	TCAGTTGTCATTTCT[C/T]GTTTCTGGAGTGATG	1107
rs750047520	snp	A/G	1.72719e-05	0.00293865	synonymous-codon	CHD3	GRCh38.p7	17:7907451	GCCTGGAGAGATGGA[A/G]CCTGAACCTGGGTAC	1107
rs750075465	snp	C/T	8.30751e-05	0.00644443	missense	CHD3	GRCh38.p7	17:7901290	AGGGTGGGGCACTTA[C/T]TAAGTCGTCTGGGAA	1107
rs750087267	snp	C/T	1.6476e-05	0.00287014	missense	CHD3	GRCh38.p7	17:7893903	AAAATAAAACTAGGG[C/T]TTCTGGGTGGCAAGA	1107
rs750092991	snp	A/G	1.65963e-05	0.0028806	intron-variant	CHD3	GRCh38.p7	17:7889149	CCTCTTGGCAAAAGG[A/G]TGTCAGGGCCCCAGG	1107
rs750172975	in-del	-/ACAC			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884073	TCATGCCCCCCCAAC[-/ACAC]ACACACACACACACA	1107
rs750205250	snp	G/T	1.72749e-05	0.0029389	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906704	AAAAAGAAGGTATCA[G/T]TCTTCCTGTCACCCA	1107
rs750206690	snp	A/G	1.64806e-05	0.00287054	missense	CHD3	GRCh38.p7	17:7899439	CCCAAATTCTATGTG[A/G]TGACATACACGGGTG	1107
rs750291146	snp	C/T	1.64931e-05	0.00287163	synonymous-codon	CHD3	GRCh38.p7	17:7893815	TTCAGGTCCAGGCCA[C/T]AAGAGGCGGAGTAAG	1107
rs750291304	snp	C/T	1.65356e-05	0.00287533	stop-gained	CHD3	GRCh38.p7	17:7907956	CCACGGTCCAATGGG[C/T]GACGAGAGGAAAAGA	1107
rs750459632	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	CHD3	GRCh38.p7	17:7897127	AAACTACCAGCGGAA[A/G]AATGACATGGATGAG	1107
rs750470178	snp	C/G	3.2981e-05	0.00406071	intron-variant	CHD3	GRCh38.p7	17:7907117	TTATCACTGTGCCTT[C/G]CCCTGCAGCTACTCC	1107
rs750518131	snp	A/G	1.65356e-05	0.00287533	intron-variant	CHD3	GRCh38.p7	17:7900454	AGAGATGAGAGGTGG[A/G]GCAGATAAAATGAGC	1107
rs750540309	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7902568	TAAGCAAGCATCCCA[C/T]CACCTCATTATTGCA	1107
rs750559708	snp	A/T	4.96323e-05	0.00498133	intron-variant	CHD3	GRCh38.p7	17:7907038	CTAAACCTGGTAATC[A/T]GAAGTCAGGATGGTG	1107
rs750564352	snp	C/G	1.65012e-05	0.00287234	missense	CHD3	GRCh38.p7	17:7894190	GGCAGTGTCCACAGT[C/G]CCTCAGGCCGGCCTG	1107
rs750594284	snp	C/G	2.77951e-05	0.00372784	missense, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884969	GGAGTACTCGGGCGC[C/G]GGCCGGGCCACGACC	1107
rs750659358	snp	C/T	3.29473e-05	0.00405864	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905091	ACTGGGCCCTTTCCA[C/T]CCCCACAGACAACCA	1107
rs750700699	snp	A/G	1.64749e-05	0.00287005	missense	CHD3	GRCh38.p7	17:7897195	GGAAGAGCGACAAGC[A/G]TAAAGTGAAAGACCC	1107
rs750733716	in-del	-/A	6.68204e-05	0.00577977	intron-variant	CHD3	GRCh38.p7	17:7908522	CCTGTATCCTTTGAT[-/A]ACACATGCAAGAAGG	1107
rs750749834	snp	A/G	0.000148688	0.00862101	synonymous-codon	CHD3	GRCh38.p7	17:7893409	AGCTGCTGTGGCGGC[A/G]GCAGCGGCAGCAGCA	1107
rs750752143	snp	G/T	1.64868e-05	0.00287109	intron-variant	CHD3	GRCh38.p7	17:7911438	TGATCTGGAGATTGA[G/T]CTTTCCTTACCCCTT	1107
rs750770566	snp	A/C	1.7383e-05	0.00294808	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906148	CCTGGGGGGTGGTCT[A/C]AGCCCACTCCACCTC	1107
rs750811816	snp	G/T	3.37291e-05	0.00410651	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906089	GTGACCTTACTCAAC[G/T]GATTATCACCCTCCC	1107
rs750856356	snp	C/T	3.74763e-05	0.0043286	intron-variant	CHD3	GRCh38.p7	17:7907581	CATCCTCCCTTCCTA[C/T]CCCCTACCCCCTCCC	1107
rs750881384	in-del	-/TT	3.30278e-05	0.0040636	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905217	CGTTTTATTTTCCAG[-/TT]TTTGCTTTAAGCCCA	1107
rs750897999	snp	A/C	1.65029e-05	0.00287248	intron-variant	CHD3	GRCh38.p7	17:7900253	CACTTGTCACTAATA[A/C]GCCCATTTTCCTGCC	1107
rs750901518	snp	C/T	1.64898e-05	0.00287135	missense, synonymous-codon	CHD3	GRCh38.p7	17:7911524	TGGTGGGGGCATTGG[C/T]GTCAGACGGGCTGGA	1107
rs750944395	snp	G/T	1.66449e-05	0.00288482	intron-variant	CHD3	GRCh38.p7	17:7908543	TGCAAGAAGGAAAAG[G/T]TTCTCTCAAGCTGGC	1107
rs750945318	snp	C/T			utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912300	GGTTGGGTGATACTC[C/T]CTCAAGCCAAAGAGG	1107
rs750972677	in-del	-/A			intron-variant	CHD3	GRCh38.p7	17:7896228	GCGACACTCTATCTC[-/A]AAAAAAAAAAAAAAA	1107
rs750990975	snp	A/T	1.84082e-05	0.00303377	synonymous-codon	CHD3	GRCh38.p7	17:7903484	TGGCACTGAAGAGCT[A/T]TTCAAGGATGAAAAC	1107
rs751026560	snp	C/T	1.65343e-05	0.00287521	intron-variant	CHD3	GRCh38.p7	17:7907594	TATCCCCTACCCCCT[C/T]CCACAGCCACAGAGT	1107
rs751040698	snp	A/C	1.71275e-05	0.00292634	intron-variant	CHD3	GRCh38.p7	17:7894630	ACCTAATGCCAGCAT[A/C]TGATGGCCCTGAGGA	1107
rs751065542	snp	C/T	2.17654e-05	0.00329882	intron-variant	CHD3	GRCh38.p7	17:7898642	TGGAGTGATGGTGAT[C/T]GAAGATTTTCCAAGG	1107
rs751074240	snp	A/G	1.85723e-05	0.00304727	missense	CHD3	GRCh38.p7	17:7908423	ACACACTGTGGCAGA[A/G]TGAGGAACGGGCAGC	1107
rs751080294	snp	A/G	3.35762e-05	0.00409719	missense	CHD3	GRCh38.p7	17:7894923	GCCCCCTAGGAGAAG[A/G]AGGGGGTCCAGTGGG	1107
rs751100930	snp	C/T	1.68724e-05	0.00290446	intron-variant	CHD3	GRCh38.p7	17:7902561	GTTAGAATAAGCAAG[C/T]ATCCCACCACCTCAT	1107
rs751126466	snp	A/C	3.32381e-05	0.00407651	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910553	CGCAGCATCCTCAGC[A/C]GGCTGGCCAGCAAGG	1107
rs751212280	snp	C/T	3.93368e-05	0.00443473	intron-variant	CHD3	GRCh38.p7	17:7890565	ATTTTTATTTCTTTC[C/T]CTTAGGACAGTGAGG	1107
rs751228376	snp	A/C	1.76365e-05	0.0029695	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906164	AGCCCACTCCACCTC[A/C]CCTCAGCCGAGCCTA	1107
rs751239875	in-del	-/GAA	1.65143e-05	0.00287348	intron-variant	CHD3	GRCh38.p7	17:7899223	GGATTCTAGGACCTT[-/GAA]GGGGACCGCCTGGAC	1107
rs751242177	snp	C/T	1.64827e-05	0.00287073	synonymous-codon, missense	CHD3	GRCh38.p7	17:7911465	CCTTTCCCAAACAGC[C/T]GCCACCAACGGCCCT	1107
rs751264217	snp	C/T	3.29734e-05	0.00406025	missense	CHD3	GRCh38.p7	17:7893934	GGAAGAAAGGAGGCT[C/T]GGTGAGTGACCCGTC	1107
rs751267937	snp	C/T			synonymous-codon	CHD3	GRCh38.p7	17:7899175	GACCATACAAACCAT[C/T]GTCTTCCTCTACTCA	1107
rs751276558	snp	C/T	3.30464e-05	0.00406474	synonymous-codon	CHD3	GRCh38.p7	17:7907003	TCCTGAGGCTTCTGC[C/T]ACCAACAGTCCCTGC	1107
rs751290768	snp	A/G	1.64768e-05	0.00287021	synonymous-codon	CHD3	GRCh38.p7	17:7897121	GTATCGAAACTACCA[A/G]CGGAAGAATGACATG	1107
rs751294356	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7896528	CTCCTGCCTCAGCCA[C/T]TCAAGTAGCTGGGAT	1107
rs751295206	in-del	-/C	3.39524e-05	0.00412008	intron-variant	CHD3	GRCh38.p7	17:7894908	TGTGTCTATCCTTGG[-/C]CCCCCTAGGAGAAGG	1107
rs751355886	snp	C/T	2.44185e-05	0.00349409	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889776	AAAACGCAAGAAGCG[C/T]GTAAGTGTCAAGAAT	1107
rs751372443	snp	A/G	1.71349e-05	0.00292697	missense	CHD3	GRCh38.p7	17:7908464	GGGAAACTCAATGAG[A/G]TCTGGCACAGAAGAC	1107
rs751372667	snp	C/T	1.68803e-05	0.00290515	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904423	ACCCCCAGTGTTCAT[C/T]CATTCTGTTGCCCTT	1107
rs751473230	snp	A/C	1.65737e-05	0.00287864	missense	CHD3	GRCh38.p7	17:7901310	TCGTCTGGGAAGCTC[A/C]TGCTGCTCCAGAAGA	1107
rs751504345	snp	C/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895452	AGATGTCCCACCCCC[C/G]CGTCCTCTTCAAGGC	1107
rs751533988	snp	C/G	1.66161e-05	0.00288232	intron-variant	CHD3	GRCh38.p7	17:7910830	TAACTCCAACTTCTG[C/G]TTCCTCTCTGTTCCA	1107
rs751546224	snp	A/G	9.74564e-05	0.00697988	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890708	GAAGAAGACAAAGCG[A/G]CGGAAAAAGGGGGAG	1107
rs751561206	snp	A/G	1.83602e-05	0.00302982	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904650	GATGCAGGCAGTAAA[A/G]GGGGGAAGTGATGAT	1107
rs751571495	snp	A/G	0.000135115	0.00821821	intron-variant	CHD3	GRCh38.p7	17:7901038	ACGCCCATTCTCAGA[A/G]AACATGGGTGGGGAG	1107
rs751588788	in-del	-/TCAACTGATTATCACCCTCCGG	1.68451e-05	0.00290211	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906083	ATGATGTGACCTTAC[-/TCAACTGATTATCACCCTCCGG]TCAACTGATTATCAC	1107
rs751611095	snp	C/G	3.82168e-05	0.00437115	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905577	GAGGACTGAGGCTTA[C/G]AGGAGGTGGTGGCTC	1107
rs751641156	snp	A/G	1.66657e-05	0.00288662	missense	CHD3	GRCh38.p7	17:7894265	AGGAAGAAGAAGAAG[A/G]GTAAGGAGTGTTGAC	1107
rs751650978	snp	A/G	1.64991e-05	0.00287215	missense	CHD3	GRCh38.p7	17:7907219	AGCCAGAGAAGAACA[A/G]CAGAATTGGGGAGAA	1107
rs751684167	snp	C/G	1.67725e-05	0.00289585	intron-variant	CHD3	GRCh38.p7	17:7897949	TTCCTCCTGCTCCTC[C/G]CCATGGCCTCCTGCC	1107
rs751701613	snp	A/G	3.31274e-05	0.00406972	intron-variant	CHD3	GRCh38.p7	17:7890904	TGGAATAGGGGCTGG[A/G]GGAGCACCTACTTCA	1107
rs751708716	snp	C/T	4.97055e-05	0.00498501	intron-variant	CHD3	GRCh38.p7	17:7891088	AGACTGGGGAATCCT[C/T]GCTAATTGACACTTT	1107
rs751715336	snp	A/G	0.000115404	0.0075953	missense, downstream-variant-500B	CHD3	GRCh38.p7	17:7903020	ACTGCTGACACTGTC[A/G]TCATCTTTGATTCTG	1107
rs751740188	snp	C/T	1.65318e-05	0.002875	intron-variant	CHD3	GRCh38.p7	17:7899302	ACTAGGGTATACGGC[C/T]TCTAGCCTAGACTTA	1107
rs751799697	snp	A/G	6.65657e-05	0.00576875	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910879	CTACGCTACACCTCC[A/G]GGGTACGGGGCGGCC	1107
rs751803023	snp	C/T	1.6549e-05	0.0028765	intron-variant, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902915	GGTACAAGAAAAACC[C/T]GATCCAACTCTCACC	1107
rs751849363	snp	A/G	1.64738e-05	0.00286995	missense	CHD3	GRCh38.p7	17:7900312	GGGTTCTCAATGGTT[A/G]CAAGATAGATCATAA	1107
rs751880641	snp	C/G			utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912653	CCCTTCACTTTCTTG[C/G]TGCCCCTTTCCCAGT	1107
rs751901666	snp	C/T	1.65343e-05	0.00287521	synonymous-codon	CHD3	GRCh38.p7	17:7908812	ATGAAAAATAAGTTC[C/T]TGGCCCGGAGGTTCA	1107
rs751902458	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7892040	ACGGGGAATAATAAT[A/G]TATACCTCATAGGAA	1107
rs751918903	snp	C/T	3.88531e-05	0.00440738	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911637	CCCGAGGCCGACCCC[C/T]AGCTCAAGCGCTGGG	1107
rs751939504	snp	A/G/T	0.000220304	0.0104933	intron-variant	CHD3	GRCh38.p7	17:7903510	AAAACGAGGGTGAGA[A/G/T]CCTTTTCTGCAGCTC	1107
rs751952458	snp	A/T	1.64735e-05	0.00286993	intron-variant, missense	CHD3	GRCh38.p7	17:7889028	GACACTGTGATCCTG[A/T]GGGCAAGAAGTAAAA	1107
rs751991299	snp	C/T	5.85634e-05	0.00541094	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906294	GGCAGGAGGAGCTGG[C/T]GGAAAGGATGAAGAG	1107
rs752010370	snp	C/T	1.64961e-05	0.00287189	missense	CHD3	GRCh38.p7	17:7911541	TCAGACGGGCTGGAT[C/T]GGAAGGAGCCCCGAG	1107
rs752055513	snp	A/G	3.29522e-05	0.00405894	synonymous-codon	CHD3	GRCh38.p7	17:7897211	TAAAGTGAAAGACCC[A/G]CACTATGCTGAGATG	1107
rs752103345	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	CHD3	GRCh38.p7	17:7895063	GCTCCTGTGCTGTGA[C/T]GCGTGCATCTCCTCC	1107
rs752113004	snp	C/T	1.90347e-05	0.00308497	missense	CHD3	GRCh38.p7	17:7909213	ACCTGTCGCAGGAGC[C/T]GGCGCACCCCGCCAT	1107
rs752113805	snp	A/G	3.29723e-05	0.00406018	missense	CHD3	GRCh38.p7	17:7907134	CCTGCAGCTACTCCA[A/G]CTCCAAGTGAGAAAG	1107
rs752119703	snp	C/T	1.70784e-05	0.00292214	intron-variant	CHD3	GRCh38.p7	17:7911017	ACTCACACTCCTCCT[C/T]TGCCAAACTTTATTT	1107
rs752189740	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7909880	CCAAAGCCCTCTAAC[C/T]ATCTAATCCTGCCTG	1107
rs752245914	snp	A/G	4.96734e-05	0.0049834	intron-variant	CHD3	GRCh38.p7	17:7899248	GCCTGGACTGGGGAA[A/G]TGGGGAGGGGGAAGA	1107
rs752259304	snp	A/G	1.77187e-05	0.00297641	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906173	CACCTCCCCTCAGCC[A/G]AGCCTAGAGTAGAGG	1107
rs752285030	snp	A/G	9.06577e-05	0.00673206	utr-variant-3-prime, synonymous-codon	CHD3	GRCh38.p7	17:7911647	ACCCCCAGCTCAAGC[A/G]CTGGGGCCTGCTGCC	1107
rs752312375	snp	A/G	5.84129e-05	0.00540398	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7907677	GGAGAGGCCGGAGGG[A/G]GAAACAGGGGATTTG	1107
rs752365619	snp	G/T	1.64789e-05	0.0028704	missense	CHD3	GRCh38.p7	17:7903878	GACAATGAGGCCATC[G/T]CTCGGCTGTTGGACC	1107
rs752389228	snp	C/T	0.000234024	0.0108147	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910582	GGGCACGGAGCCTCA[C/T]CCCACACCGGTAACC	1107
rs752402023	snp	A/G	1.65127e-05	0.00287334	missense	CHD3	GRCh38.p7	17:7894953	GAGGCCAAGGAGGAA[A/G]AAGAAGAATACGAAG	1107
rs752411930	snp	C/G	1.64741e-05	0.00286998	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905080	CCTCCCTGACCACTG[C/G]GCCCTTTCCACCCCC	1107
rs752425204	in-del	-/CCA	0.0191018	0.0958438	cds-indel, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885046	CCGCCGCCGCCGCCG[-/CCA]CCACCGCTGCCCCCG	1107
rs752437456	snp	A/G	2.60909e-05	0.00361176	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890582	TTAGGACAGTGAGGA[A/G]GAATTTGGTTCTGAG	1107
rs752446870	in-del	-/TTCA	0.000135582	0.0082324	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904418	AGGAGACCCCCAGTG[-/TTCA]TTCATTCTGTTGCCC	1107
rs752499617	snp	C/T	1.64969e-05	0.00287196	intron-variant	CHD3	GRCh38.p7	17:7907101	GGGAGAATCTCTGTC[C/T]TTATCACTGTGCCTT	1107
rs752502688	snp	C/G			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904983	TGTTCCCAGAAGGAC[C/G]AAGGCCAGAATAAAG	1107
rs752517649	snp	A/G	0.000151016	0.00868821	synonymous-codon	CHD3	GRCh38.p7	17:7901348	AAAGCTGAAGGAGCA[A/G]GGACACCGAGTGCTC	1107
rs752525306	snp	A/G	4.15619e-05	0.00455842	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890659	GAACCGGACCGGGTC[A/G]GAAACGAAGAAGGAA	1107
rs752585420	snp	A/G	4.57823e-05	0.00478425	missense, intron-variant	CHD3	GRCh38.p7	17:7907607	CTCCCACAGCCACAG[A/G]GTCGACGCCAGGAGA	1107
rs752600370	snp	A/G	1.82075e-05	0.00301719	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904652	TGCAGGCAGTAAAGG[A/G]GGGAAGTGATGATGA	1107
rs752621737	snp	C/T	6.58935e-05	0.00573955	synonymous-codon	CHD3	GRCh38.p7	17:7899130	CCAGGGCACTGACAC[C/T]ATTCTAGCTGATGAG	1107
rs752667381	snp	C/G	1.65515e-05	0.00287671	missense	CHD3	GRCh38.p7	17:7907970	GCGACGAGAGGAAAA[C/G]ACAGAGAAGCCCCGG	1107
rs752695969	snp	G/T	1.66043e-05	0.00288129	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903070	CATCCAGGTGGGAAC[G/T]CGCATCCTAGAACCC	1107
rs752699052	snp	A/G	0.000182156	0.00954174	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906217	CCCCAGGGGAGGGGC[A/G]TTGAAGCAAGGAGCC	1107
rs752709646	snp	C/G	1.66538e-05	0.00288559	intron-variant	CHD3	GRCh38.p7	17:7902598	AGACTCCATCCTTTT[C/G]TCTTGCTCTAGATGA	1107
rs752721648	snp	C/T	5.05906e-05	0.00502919	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910924	CGTAGGGGCCCTGGC[C/T]GCCGCAGGCGCCAAT	1107
rs752730668	in-del	-/CT	0.00247218	0.0350711	intron-variant	CHD3	GRCh38.p7	17:7909425	AAATCTTCCCACCCC[-/CT]GACCCCTCTACCTGC	1107
rs752769159	snp	A/G	3.30158e-05	0.00406286	intron-variant	CHD3	GRCh38.p7	17:7891069	CAGTTCATGAGGTGC[A/G]GTAAGACTGGGGAAT	1107
rs752783832	snp	C/T	3.29679e-05	0.00405991	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905870	GGTGCTGGGCTTCAA[C/T]ACCCGTCAGCGGAAG	1107
rs752804573	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7892152	GACTGTCATTAGTAA[C/T]GTTGTCTCACCTACC	1107
rs752811295	snp	A/G	4.99804e-05	0.00499877	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910888	ACCTCCGGGGTACGG[A/G]GCGGCCTTCAGCGCC	1107
rs752833740	snp	A/G	1.6501e-05	0.00287232	missense, intron-variant	CHD3	GRCh38.p7	17:7895345	ATCCCAAAGTGCCCC[A/G]TGCTGAAGGGTCGAG	1107
rs752856574	snp	C/T	1.66977e-05	0.00288939	intron-variant	CHD3	GRCh38.p7	17:7899859	TAGGTGCATGGTTGT[C/T]AGGTGGCAGCTGAAT	1107
rs752948131	snp	C/G	1.64914e-05	0.00287149	missense	CHD3	GRCh38.p7	17:7899470	ACAAGGACAGCCGGG[C/G]CATCATTCGTGAGAA	1107
rs752964342	snp	A/G	1.74111e-05	0.00295047	intron-variant	CHD3	GRCh38.p7	17:7908052	TGCTTTCTGCTCCTC[A/G]AGGGGATCTGCTCAT	1107
rs752967338	snp	A/G	8.52173e-05	0.00652698	intron-variant	CHD3	GRCh38.p7	17:7894401	CCTTATCCCTCCACC[A/G]GGGTATATGACAGTC	1107
rs753028982	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7889160	AAGGATGTCAGGGCC[C/T]CAGGGTGTTAGTGTG	1107
rs753046059	snp	A/G	1.64982e-05	0.00287208	intron-variant	CHD3	GRCh38.p7	17:7889119	ATTATCCGAGGAAAT[A/G]TAAATAGAGGCCTCC	1107
rs753088868	snp	C/G	8.25989e-05	0.00642593	intron-variant	CHD3	GRCh38.p7	17:7900783	GGGATTGATGGGAGC[C/G]TTCCAAGTGCAATAT	1107
rs753157504	snp	C/T	0.000138629	0.00832438	synonymous-codon	CHD3	GRCh38.p7	17:7909247	CCTCCACGCCCGCTT[C/T]GCCGAGGCCGAGTGC	1107
rs753165289	snp	A/G	1.68482e-05	0.00290238	intron-variant	CHD3	GRCh38.p7	17:7894297	GTGTGTGATCCTGTC[A/G]GTGGGCCGTCCTCTC	1107
rs753191510	snp	A/G	1.6473e-05	0.00286988	intron-variant, missense	CHD3	GRCh38.p7	17:7889044	GGGCAAGAAGTAAAA[A/G]TGACCAGCTGAGGAT	1107
rs753253748	snp	A/T			intron-variant	CHD3	GRCh38.p7	17:7898303	GGCTGAGTAGTGGAG[A/T]AGAGGATGTTCAAGA	1107
rs753264591	snp	C/T	3.16131e-05	0.00397562	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905616	GATGTCATCCCCACC[C/T]TCAGGGCGTAGACAG	1107
rs753265805	snp	A/C	1.69195e-05	0.00290851	intron-variant	CHD3	GRCh38.p7	17:7907318	AGGTACCTGGGAGCC[A/C]TCTGGCTCATCCTGA	1107
rs753285040	snp	G/T	4.99888e-05	0.00499919	intron-variant	CHD3	GRCh38.p7	17:7897962	TCCCCATGGCCTCCT[G/T]CCCCACAGTGTGGAT	1107
rs753325245	snp	A/C	1.65231e-05	0.00287424	intron-variant	CHD3	GRCh38.p7	17:7889134	GTAAATAGAGGCCTC[A/C]CTCTTGGCAAAAGGA	1107
rs753338393	snp	G/T	1.64735e-05	0.00286993	intron-variant, synonymous-codon	CHD3	GRCh38.p7	17:7889063	CCAGCTGAGGATTTC[G/T]TTTCCTCCAGGACTG	1107
rs753346769	snp	G/T	1.65051e-05	0.00287267	splice-acceptor-variant	CHD3	GRCh38.p7	17:7893804	CCGACTCCTCATTCA[G/T]GTCCAGGCCATAAGA	1107
rs753364756	snp	A/G	3.33217e-05	0.00408163	intron-variant	CHD3	GRCh38.p7	17:7904007	GTGAGAGGCTTTGGG[A/G]GCCAGACATTATCTA	1107
rs753425177	snp	G/T	1.67337e-05	0.00289251	intron-variant	CHD3	GRCh38.p7	17:7901019	AGAGCAGGGAGCTGA[G/T]CGAACGCCCATTCTC	1107
rs753427196	snp	G/T	1.64776e-05	0.00287028	missense	CHD3	GRCh38.p7	17:7898014	CTAGTAAAATGGAGG[G/T]ACTTACCATATGACC	1107
rs753438058	snp	C/T	8.9312e-05	0.00668192	intron-variant	CHD3	GRCh38.p7	17:7910305	GTTCTTTGACATCTG[C/T]GTTCTCCTCTCTCGC	1107
rs753458057	snp	C/T	0.000337439	0.0129848	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904159	AGAGAGAAACGTAGG[C/T]ACAGACAGTACTGGT	1107
rs753462940	snp	A/G			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886338	CTTTGGGATAGGTGA[A/G]CATCTGGGTGTCCAC	1107
rs753517072	snp	C/T	1.6519e-05	0.00287388	intron-variant	CHD3	GRCh38.p7	17:7900823	TTCCTTTATTTATGT[C/T]TCTTTTACACCCCTT	1107
rs753541191	snp	A/C	3.67343e-05	0.00428553	intron-variant	CHD3	GRCh38.p7	17:7893587	AGGGAACTCTCTTCC[A/C]ACAACTGTCATCTCA	1107
rs753543087	snp	A/T	1.66399e-05	0.00288438	intron-variant	CHD3	GRCh38.p7	17:7895312	TGCCTCTTTCTTTCC[A/T]CCTCCTTGTACGTGT	1107
rs753556725	snp	A/G	1.65828e-05	0.00287943	intron-variant, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902905	AGAACTACCGGGTAC[A/G]AGAAAAACCTGATCC	1107
rs753570738	snp	C/G/T	3.30569e-05	0.00406541	intron-variant	CHD3	GRCh38.p7	17:7890899	CGGCCTGGAATAGGG[C/G/T]CTGGAGGAGCACCTA	1107
rs753601572	snp	C/T			intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906484	CCTCAGTCATCCTCG[C/T]GCCTCCCTCACTGCC	1107
rs753646580	snp	A/G	6.87971e-05	0.00586462	intron-variant	CHD3	GRCh38.p7	17:7907709	GCAAGAGAGGTAATG[A/G]GTGGAAGGGACCGGA	1107
rs753648357	snp	A/C	1.66205e-05	0.00288271	missense	CHD3	GRCh38.p7	17:7910874	GGTCCCTACGCTACA[A/C]CTCCGGGGTACGGGG	1107
rs753657586	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7892413	TATGAACTGTAAAGT[A/C]GTATACAAAAGTAAA	1107
rs753702435	snp	C/G	1.64838e-05	0.00287083	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905202	CTACCTCACCTCTTC[C/G]CGTTTTATTTTCCAG	1107
rs753731518	snp	A/G	1.64857e-05	0.00287099	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906554	CCCATGCTCCTTAGG[A/G]CCTATGTGTCTTTGT	1107
rs753736107	snp	C/G	1.66283e-05	0.00288338	intron-variant	CHD3	GRCh38.p7	17:7910827	AACTAACTCCAACTT[C/G]TGCTTCCTCTCTGTT	1107
rs753736659	snp	C/T	1.65307e-05	0.0028749	synonymous-codon	CHD3	GRCh38.p7	17:7902615	CTTGCTCTAGATGAC[C/T]AAAATGTTAGACTTG	1107
rs753740590	snp	C/T	3.29489e-05	0.00405874	synonymous-codon	CHD3	GRCh38.p7	17:7895072	CTGTGACGCGTGCAT[C/T]TCCTCCTACCACATT	1107
rs753752369	snp	A/T	6.61299e-05	0.00574983	intron-variant	CHD3	GRCh38.p7	17:7899296	CAGAGGACTAGGGTA[A/T]ACGGCCTCTAGCCTA	1107
rs753770040	snp	A/G	2.31291e-05	0.00340059	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890697	GAAAAAAAGGAGAAG[A/G]AGACAAAGCGGCGGA	1107
rs753823202	in-del	-/TTATTT	0.000384862	0.0138666	intron-variant	CHD3	GRCh38.p7	17:7890548	AGGGATGAATAAATG[-/TTATTT]TTATTTCTTTCTCTT	1107
rs753826001	snp	G/T	1.6473e-05	0.00286988	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895461	ACCCCCCCGTCCTCT[G/T]CAAGGCAGATCAGAG	1107
rs753841070	snp	A/T	1.6569e-05	0.00287824	synonymous-codon	CHD3	GRCh38.p7	17:7907922	TGACCGGGAGCTTCG[A/T]CCAGGGCCTCGAGAT	1107
rs753844697	snp	A/T	1.64871e-05	0.00287111	missense	CHD3	GRCh38.p7	17:7899915	AGGCACAGGTGAAGT[A/T]CCATGTTCTCCTGAC	1107
rs753997096	snp	G/T	1.74027e-05	0.00294975	synonymous-codon	CHD3	GRCh38.p7	17:7893397	CAAGGGGTCAGCAGC[G/T]GCTGTGGCGGCGGCA	1107
rs754037512	snp	G/T	1.6543e-05	0.00287597	intron-variant	CHD3	GRCh38.p7	17:7897078	TTTTTTCTGTGCCCT[G/T]CTAGCTGGAAATCTT	1107
rs754100868	snp	C/T	1.6537e-05	0.00287545	synonymous-codon	CHD3	GRCh38.p7	17:7907018	TACCAACAGTCCCTG[C/T]ACCTCTAAACCTGGT	1107
rs754115600	in-del	-/A	1.64735e-05	0.00286993	intron-variant	CHD3	GRCh38.p7	17:7900054	GAGGTTTCCAGACCT[-/A]AAAAAACTTGAAGTT	1107
rs754127135	snp	A/T	6.60164e-05	0.0057449	intron-variant	CHD3	GRCh38.p7	17:7900248	TCGGTCACTTGTCAC[A/T]AATAAGCCCATTTTC	1107
rs754131838	snp	A/G			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888580	GTTCCCCAAGCCTTC[A/G]CAGAGTGACACCTTC	1107
rs754211179	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7902351	CACTTGAACCCAGGA[A/G]TGGAGGTTGCAGTGA	1107
rs754211502	snp	C/T	1.70232e-05	0.00291741	intron-variant	CHD3	GRCh38.p7	17:7907335	CTGGCTCATCCTGAC[C/T]CCATTGTCCTCTTCC	1107
rs754224051	snp	C/T	1.64868e-05	0.00287109	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905939	ACAGGATGCCTTCAC[C/T]ACACAGTGGCTGGTG	1107
rs754274557	snp	A/T	1.65756e-05	0.00287881	intron-variant	CHD3	GRCh38.p7	17:7891094	GGGAATCCTCGCTAA[A/T]TGACACTTTTAATTT	1107
rs754326595	snp	C/T	1.67452e-05	0.0028935	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903259	CACCCGCCACTTTCT[C/T]TTGCCCCTGCAGGCC	1107
rs754341443	snp	A/G	5.05685e-05	0.00502809	missense	CHD3	GRCh38.p7	17:7910928	GGGGCCCTGGCCGCC[A/G]CAGGCGCCAATTACA	1107
rs754386986	snp	C/T	1.66391e-05	0.00288431	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903076	GGTGGGAACTCGCAT[C/T]CTAGAACCCCTGCAC	1107
rs754416486	snp	C/T	6.65801e-05	0.00576937	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906037	GCAAGGGGAAGAGCT[C/T]TGGGTGTTCCTTTCT	1107
rs754422934	snp	C/T	1.76702e-05	0.00297234	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906168	CACTCCACCTCCCCT[C/T]AGCCGAGCCTAGAGT	1107
rs754427761	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7910261	TTGCTTCTGTTTTCC[A/G]TCTACTTCTTTTACT	1107
rs754472134	snp	C/T	1.84065e-05	0.00303363	missense	CHD3	GRCh38.p7	17:7893429	CGGCAGCAGCAGCAG[C/T]AGCTGTAGCTGAGCA	1107
rs754484755	in-del	-/T			downstream-variant-500B	CHD3	GRCh38.p7	17:7912777	CTCTGTTATTTTTTA[-/T]GGGGGGGGGGAGTTT	1107
rs754495503	snp	C/T	1.68621e-05	0.00290358	intron-variant	CHD3	GRCh38.p7	17:7898968	TAAGACTGGAGGAGC[C/T]GCCGACTATTTCCTT	1107
rs754508953	snp	C/T	1.69387e-05	0.00291016	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906102	ACTGATTATCACCCT[C/T]CCTGTCATACAATAC	1107
rs754533336	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7893765	TCCAGGATGTCATGA[A/C]CTCTCCTTTTTCCTC	1107
rs754616629	in-del	-/C	1.65638e-05	0.00287778	intron-variant	CHD3	GRCh38.p7	17:7899254	CTGGGGAAGTGGGGA[-/C]GGGGGAAGATAAAGG	1107
rs754760061	snp	A/C	0.000490184	0.0156477	intron-variant	CHD3	GRCh38.p7	17:7901040	GCCCATTCTCAGAAA[A/C]CATGGGTGGGGAGTA	1107
rs754780717	snp	C/G	2.62484e-05	0.00362264	intron-variant	CHD3	GRCh38.p7	17:7889785	GAAGCGTGTAAGTGT[C/G]AAGAATTCCTAACTC	1107
rs754798040	snp	C/T	3.51859e-05	0.00419425	intron-variant	CHD3	GRCh38.p7	17:7890568	TTTATTTCTTTCTCT[C/T]AGGACAGTGAGGAGG	1107
rs754814641	snp	A/G	1.64806e-05	0.00287054	missense	CHD3	GRCh38.p7	17:7893832	AGAGGCGGAGTAAGA[A/G]CCCCCGAGTGCCTGA	1107
rs754853963	snp	C/T	1.68343e-05	0.00290118	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904426	CCCAGTGTTCATTCA[C/T]TCTGTTGCCCTTCAG	1107
rs754854794	snp	A/G	6.58924e-05	0.0057395	missense, intron-variant	CHD3	GRCh38.p7	17:7895454	ATGTCCCACCCCCCC[A/G]TCCTCTTCAAGGCAG	1107
rs754875511	snp	A/G	1.78908e-05	0.00299084	intron-variant	CHD3	GRCh38.p7	17:7907495	AGAAGTCAGGTGGGT[A/G]CATGGCCTTAGGAGT	1107
rs754904490	snp	C/G			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904922	CGGTGAATGGAGATG[C/G]TGTAGGATATGCGGC	1107
rs754919272	snp	C/T	1.65067e-05	0.00287282	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903043	TGATTCTGACTGGAA[C/T]CCCCATAATGACATC	1107
rs754939048	snp	C/G	4.95168e-05	0.00497553	missense	CHD3	GRCh38.p7	17:7898518	ATTATGGGGGAAGAC[C/G]CTGCCCAGCCCCGCA	1107
rs754960962	snp	C/T	3.31526e-05	0.00407127	synonymous-codon	CHD3	GRCh38.p7	17:7901318	GAAGCTCATGCTGCT[C/T]CAGAAGATGCTGCGA	1107
rs754991366	snp	C/G	1.64991e-05	0.00287215	intron-variant	CHD3	GRCh38.p7	17:7890929	ACTTCACCAAAGCCC[C/G]TCTCCCGCAGCAAGT	1107
rs754993916	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7890097	CTAGGATACCAGGCC[A/G]TTTATTTGGCTCTCT	1107
rs754994882	snp	C/G	1.654e-05	0.00287571	intron-variant, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902919	CAAGAAAAACCTGAT[C/G]CAACTCTCACCTCCT	1107
rs755045743	in-del	-/AA	0.00963899	0.0687502	intron-variant	CHD3	GRCh38.p7	17:7908559	TTCTCTCAAGCTGGC[-/AA]AAAAAAAAAAGATGA	1107
rs755082550	snp	C/T	1.64776e-05	0.00287028	synonymous-codon	CHD3	GRCh38.p7	17:7902672	CTACAAGTATGAGCG[C/T]ATCGATGGTGGTATC	1107
rs755088269	snp	C/G	1.65996e-05	0.00288089	intron-variant	CHD3	GRCh38.p7	17:7910836	CAACTTCTGCTTCCT[C/G]TCTGTTCCAGGCCTA	1107
rs755097110	in-del	-/G	5.16814e-05	0.00508311	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906135	CTGGCTCGATTTCCT[-/G]GGGGGGTGGTCTCAG	1107
rs755101105	in-del	-/G	0.000167062	0.009138	intron-variant	CHD3	GRCh38.p7	17:7894100	CTCACTGACGGCCAC[-/G]GGGGCTATGGGCAGT	1107
rs755116536	snp	A/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904649	AGATGCAGGCAGTAA[A/T]GGGGGGAAGTGATGA	1107
rs755135935	in-del	-/T			intron-variant	CHD3	GRCh38.p7	17:7892802	CCCAGCCTATTTCCC[-/T]TTTTTTTAAAGACAG	1107
rs755189107	snp	A/G	1.65296e-05	0.00287481	intron-variant	CHD3	GRCh38.p7	17:7899307	GGTATACGGCCTCTA[A/G]CCTAGACTTATGCTG	1107
rs755194124	snp	C/T	3.30191e-05	0.00406306	missense	CHD3	GRCh38.p7	17:7894203	GTGCCTCAGGCCGGC[C/T]TGATGGCCCTGTCCG	1107
rs755213581	snp	C/T			downstream-variant-500B	CHD3, LOC284023	GRCh38.p7	17:7912908	ACTAAAACTGAGGTT[C/T]TTCCAGCCCCAGCTA	1107
rs755213640	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7896035	GATCGAGACTATCCT[A/G]GCTAACATGGTGAAA	1107
rs755247003	snp	A/G	3.31625e-05	0.00407188	intron-variant	CHD3	GRCh38.p7	17:7900514	CTGAGATCAGGGGCA[A/G]GGAACTTGCCGACCT	1107
rs755261950	snp	C/T	2.46345e-05	0.00350951	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890709	AAGAAGACAAAGCGG[C/T]GGAAAAAGGGGGAGG	1107
rs755268649	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7898684	AACTTCCCAGAGATT[C/T]AGTAACCTCTGTGAA	1107
rs755284132	snp	A/T	5.01291e-05	0.0050062	intron-variant	CHD3	GRCh38.p7	17:7894274	AAGAAGGGTAAGGAG[A/T]GTTGACTGTGTGTGA	1107
rs755334922	snp	A/G	1.648e-05	0.0028705	missense	CHD3	GRCh38.p7	17:7903869	ATTCATTATGACAAT[A/G]AGGCCATCGCTCGGC	1107
rs755345554	snp	A/G	1.64746e-05	0.00287002	missense	CHD3	GRCh38.p7	17:7897159	CCCCACCCCTGGACT[A/G]TGGCTCCGGCGAGGA	1107
rs755406587	snp	A/G	8.29084e-05	0.00643796	intron-variant	CHD3	GRCh38.p7	17:7908838	GTTCAAGGTGGGAAT[A/G]AGGGAGGAAAGGAGC	1107
rs755506653	snp	C/G	1.6486e-05	0.00287102	missense	CHD3	GRCh38.p7	17:7907135	CTGCAGCTACTCCAG[C/G]TCCAAGTGAGAAAGG	1107
rs755545431	snp	A/G			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886539	TTGGGGGAGCGGGGG[A/G]TGCTTTCTTGTGGGT	1107
rs755558715	snp	C/T	1.64781e-05	0.00287033	synonymous-codon	CHD3	GRCh38.p7	17:7903880	CAATGAGGCCATCGC[C/T]CGGCTGTTGGACCGG	1107
rs755559882	snp	A/G	4.94849e-05	0.00497393	intron-variant, utr-variant-5-prime	CHD3	GRCh38.p7	17:7888974	AGGAGGAATATTTAG[A/G]TAATTGTGGAGACTT	1107
rs755607305	snp	C/T	1.64966e-05	0.00287194	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906534	CCCCTAACCCTCCTC[C/T]CACTCCCATGCTCCT	1107
rs755648643	snp	C/G	4.25777e-05	0.00461379	intron-variant	CHD3	GRCh38.p7	17:7903546	AAGCAGGCCCCTGCT[C/G]TCTCAGGAGTACTTA	1107
rs755665866	snp	A/C	0.000108474	0.00736376	synonymous-codon	CHD3	GRCh38.p7	17:7893565	CAAAACCAAAGAGGG[A/C]AAAGGTAGGGAACTC	1107
rs755774422	snp	A/G	1.65081e-05	0.00287293	synonymous-codon	CHD3	GRCh38.p7	17:7894958	CAAGGAGGAAGAAGA[A/G]GAATACGAAGAGGAG	1107
rs755801203	snp	A/G	5.34736e-05	0.00517049	missense	CHD3	GRCh38.p7	17:7909248	CTCCACGCCCGCTTC[A/G]CCGAGGCCGAGTGCC	1107
rs755840598	snp	G/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904998	CAAGGCCAGAATAAA[G/T]GTAGACAAGTCTCGG	1107
rs755867128	snp	C/T	3.29495e-05	0.00405877	missense	CHD3	GRCh38.p7	17:7895065	TCCTGTGCTGTGACG[C/T]GTGCATCTCCTCCTA	1107
rs755881547	snp	A/T			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883455	CAGTTGAATTTTACA[A/T]TCTAACAATTGGAGG	1107
rs755886972	snp	A/G	1.66065e-05	0.00288149	intron-variant	CHD3	GRCh38.p7	17:7902603	CCATCCTTTTCTCTT[A/G]CTCTAGATGACCAAA	1107
rs755897000	snp	A/T	1.68823e-05	0.00290532	synonymous-codon	CHD3	GRCh38.p7	17:7901357	GGAGCAAGGACACCG[A/T]GTGCTCATCTTCTCG	1107
rs755920474	snp	C/T	1.68252e-05	0.0029004	intron-variant	CHD3	GRCh38.p7	17:7898977	AGGAGCCGCCGACTA[C/T]TTCCTTGAGCTTTCT	1107
rs755976273	snp	C/T	3.29473e-05	0.00405864	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905087	GACCACTGGGCCCTT[C/T]CCACCCCCACAGACA	1107
rs755986097	snp	A/G	2.86816e-05	0.00378682	intron-variant	CHD3	GRCh38.p7	17:7889796	GTGTCAAGAATTCCT[A/G]ACTCTGTGGCAAGGC	1107
rs756035506	snp	G/T			intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906377	GGGTGGGGCGCAGGG[G/T]GACAGTTAGGACTTG	1107
rs756052160	snp	C/G	1.78201e-05	0.00298491	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906187	CGAGCCTAGAGTAGA[C/G]GGGCCAGGCATCCTC	1107
rs756074044	snp	A/G	2.3693e-05	0.0034418	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890590	GTGAGGAGGAATTTG[A/G]TTCTGAGCGAGATGA	1107
rs756135669	snp	A/G	3.29864e-05	0.00406105	missense	CHD3	GRCh38.p7	17:7899472	AAGGACAGCCGGGCC[A/G]TCATTCGTGAGAATG	1107
rs756184325	snp	C/T	6.59413e-05	0.00574163	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895377	GCAGAAGATCCTACA[C/T]TGGCGGTGGGGGGAG	1107
rs756195804	in-del	-/A			intron-variant	CHD3	GRCh38.p7	17:7909552	TGTCTGATAGCATTC[-/A]ACATCCGTGCCCAAT	1107
rs756228318	snp	A/G	1.65718e-05	0.00287848	missense	CHD3	GRCh38.p7	17:7907974	CGAGAGGAAAAGACA[A/G]AGAAGCCCCGGTTCA	1107
rs756257143	snp	C/T	1.66153e-05	0.00288225	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903071	ATCCAGGTGGGAACT[C/T]GCATCCTAGAACCCC	1107
rs756289661	in-del	-/CTC	1.77909e-05	0.00298247	intron-variant	CHD3	GRCh38.p7	17:7910309	TTTGACATCTGTGTT[-/CTC]CTCTCTCGCTCTTTT	1107
rs756342231	snp	A/G	8.24436e-05	0.00641989	intron-variant	CHD3	GRCh38.p7	17:7890936	CAAAGCCCCTCTCCC[A/G]CAGCAAGTGGAACAG	1107
rs756353717	snp	A/T	1.74758e-05	0.00295594	intron-variant	CHD3	GRCh38.p7	17:7908058	CTGCTCCTCAAGGGG[A/T]TCTGCTCATCCTCAT	1107
rs756423346	snp	A/G	1.68843e-05	0.00290549	intron-variant	CHD3	GRCh38.p7	17:7894301	GTGATCCTGTCAGTG[A/G]GCCGTCCTCTCATTC	1107
rs756430092	snp	A/C/G	1.65252e-05	0.00287443	intron-variant	CHD3	GRCh38.p7	17:7891078	AGGTGCGGTAAGACT[A/C/G]GGGAATCCTCGCTAA	1107
rs756538652	in-del	-/G	1.68136e-05	0.0028994	frameshift-variant	CHD3	GRCh38.p7	17:7894921	GGCCCCCTAGGAGAA[-/G]GGAGGGGGTCCAGTG	1107
rs756565340	snp	A/G	1.65097e-05	0.00287308	synonymous-codon	CHD3	GRCh38.p7	17:7907241	TGGGGAGAAGATGGA[A/G]ACAGAGGTGTGTGGC	1107
rs756569009	snp	A/G	0.000116763	0.00763989	missense	CHD3	GRCh38.p7	17:7910889	CCTCCGGGGTACGGG[A/G]CGGCCTTCAGCGCCG	1107
rs756575816	snp	A/T	1.64732e-05	0.0028699	intron-variant, missense	CHD3	GRCh38.p7	17:7889047	CAAGAAGTAAAAATG[A/T]CCAGCTGAGGATTTC	1107
rs756671554	snp	C/T	4.94401e-05	0.00497168	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905894	GCGGAAGGCTTTCCT[C/T]AATGCTGTGATGCGC	1107
rs756687052	snp	G/T	8.25812e-05	0.00642524	missense	CHD3	GRCh38.p7	17:7894214	CGGCCTGATGGCCCT[G/T]TCCGCACCAAGAAAC	1107
rs756701664	snp	C/T	3.30224e-05	0.00406326	intron-variant	CHD3	GRCh38.p7	17:7900837	TTTCTTTTACACCCC[C/T]TTCCTGGCCTTTAGG	1107
rs756734148	snp	A/G			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883685	TCCCGCTTCTCATTT[A/G]AAAGATATGTACACA	1107
rs756735238	snp	C/T	1.74546e-05	0.00295415	synonymous-codon	CHD3	GRCh38.p7	17:7909268	GGCCGAGTGCCTGGC[C/T]GAGAGCCACCAGCAC	1107
rs756751514	snp	C/G	1.66738e-05	0.00288732	intron-variant	CHD3	GRCh38.p7	17:7904008	TGAGAGGCTTTGGGG[C/G]CCAGACATTATCTAT	1107
rs756760970	in-del	-/CGGAAA	2.06567e-05	0.00321371	cds-indel	CHD3	GRCh38.p7	17:7890658	GGAACCGGACCGGGT[-/CGGAAA]CGAAGAAGGAAGCAC	1107
rs756797347	snp	A/C	1.64749e-05	0.00287005	synonymous-codon	CHD3	GRCh38.p7	17:7900652	CCACACATGCTGCGG[A/C]GACTCAAGGCAGATG	1107
rs756883072	snp	G/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905256	ATACAAGTAAAAAAG[G/T]CTTCGTGTGTGTGTG	1107
rs756884528	in-del	-/CTGA			intron-variant	CHD3	GRCh38.p7	17:7910037	CACCTCCCATGCCTC[-/CTGA]CTATTTCCTCCCCAT	1107
rs756894673	snp	A/G	1.70609e-05	0.00292065	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906686	GGAGTCATGTCTCTC[A/G]TCAAAAAGAAGGTAT	1107
rs756901424	snp	C/G/T	0.000201074	0.0100252	intron-variant	CHD3	GRCh38.p7	17:7901020	GAGCAGGGAGCTGAT[C/G/T]GAACGCCCATTCTCA	1107
rs756903420	snp	C/T	6.59044e-05	0.00574002	missense	CHD3	GRCh38.p7	17:7898020	AAATGGAGGGACTTA[C/T]CATATGACCAGTCCA	1107
rs756910211	snp	C/G	1.70281e-05	0.00291783	intron-variant	CHD3	GRCh38.p7	17:7907336	TGGCTCATCCTGACC[C/G]CATTGTCCTCTTCCA	1107
rs756925185	snp	A/G	3.30338e-05	0.00406397	intron-variant	CHD3	GRCh38.p7	17:7907255	AGACAGAGGTGTGTG[A/G]CTCCCTGGATTCCCC	1107
rs756977152	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7892497	GTTTTTTATTTCCCC[C/T]TTTTTTTTTTTTTTT	1107
rs757000641	snp	A/C	1.64942e-05	0.00287173	missense	CHD3	GRCh38.p7	17:7893813	CATTCAGGTCCAGGC[A/C]ATAAGAGGCGGAGTA	1107
rs757002317	snp	A/C	1.77577e-05	0.00297969	intron-variant	CHD3	GRCh38.p7	17:7910311	TGACATCTGTGTTCT[A/C]CTCTCTCGCTCTTTT	1107
rs757010139	snp	A/C	1.64852e-05	0.00287094	synonymous-codon, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906556	CATGCTCCTTAGGGC[A/C]TATGTGTCTTTGTTC	1107
rs757045751	snp	C/T	3.30978e-05	0.0040679	missense	CHD3	GRCh38.p7	17:7907929	GAGCTTCGACCAGGG[C/T]CTCGAGATGAGCCAC	1107
rs757112251	snp	C/T	1.64798e-05	0.00287047	synonymous-codon	CHD3	GRCh38.p7	17:7895102	TCATTGTCTAAACCC[C/T]CCCCTGCCTGACATT	1107
rs757119137	snp	A/G	3.31422e-05	0.00407063	intron-variant, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902908	ACTACCGGGTACAAG[A/G]AAAACCTGATCCAAC	1107
rs757119865	snp	A/G	3.42202e-05	0.00413629	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906690	TCATGTCTCTCGTCA[A/G]AAAGAAGGTATCAGT	1107
rs757141050	snp	C/T	7.60659e-05	0.00616662	intron-variant	CHD3	GRCh38.p7	17:7907721	ATGGGTGGAAGGGAC[C/T]GGACACCTGGGTCCC	1107
rs757150707	snp	C/T	2.78331e-05	0.00373038	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911667	GGCCTGCTGCCAGCC[C/T]TCCACCTTCCCCACC	1107
rs757169684	in-del	-/TCTTTCTCTTGCCCT	1.65666e-05	0.00287802	intron-variant	CHD3	GRCh38.p7	17:7910388	CTCTGTATTTCCCTG[-/TCTTTCTCTTGCCCT]TCTTTCTCTGTGGCC	1107
rs757171450	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7894039	ATCCGTGAGGGATGG[C/T]GGAACAGGAAGCCAA	1107
rs757221678	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7900474	ATAAAATGAGCTGGT[A/G]GAGGATTAATCTGAG	1107
rs757259099	snp	C/T	1.65427e-05	0.00287595	missense	CHD3	GRCh38.p7	17:7907028	CCCTGCACCTCTAAA[C/T]CTGGTAATCAGAAGT	1107
rs757304805	snp	A/C/G	3.29811e-05	0.00406075	missense	CHD3	GRCh38.p7	17:7894987	AGGGAGAGGAAGAAG[A/C/G]GGAGAAGGAGGAGGA	1107
rs757319732	snp	C/T	1.65414e-05	0.00287583	intron-variant	CHD3	GRCh38.p7	17:7893948	TCGGTGAGTGACCCG[C/T]CCCTGTCTACTAAAC	1107
rs757378178	snp	A/C	0.000249478	0.0111659	missense	CHD3	GRCh38.p7	17:7910475	ATGAAGGCGGACGTG[A/C]CCCGCCTGCCAGCCA	1107
rs757406846	snp	A/G/T	3.67008e-05	0.00428361	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904654	CAGGCAGTAAAGGGG[A/G/T]GAAGTGATGATGAGT	1107
rs757429190	snp	C/T	3.29723e-05	0.00406018	synonymous-codon	CHD3	GRCh38.p7	17:7897098	CTGGAAATCTTCCAT[C/T]TGGTTATGTATCGAA	1107
rs757433731	snp	C/T	1.85568e-05	0.00304599	missense	CHD3	GRCh38.p7	17:7893405	CAGCAGCTGCTGTGG[C/T]GGCGGCAGCGGCAGC	1107
rs757490956	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7901757	CTCAGGTGATCTGCC[C/T]GCCTCGGTCTCCCAA	1107
rs757544586	snp	C/T	1.6473e-05	0.00286988	stop-gained, intron-variant	CHD3	GRCh38.p7	17:7895477	CAAGGCAGATCAGAG[C/T]GAGAGTTCTTTGTCA	1107
rs757546165	snp	A/T	1.65822e-05	0.00287938	intron-variant	CHD3	GRCh38.p7	17:7891097	AATCCTCGCTAATTG[A/T]CACTTTTAATTTGAG	1107
rs757633867	snp	C/T	1.67405e-05	0.00289309	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903099	CCCTGCACCATTTAG[C/T]AAGGAGATGTGGGTT	1107
rs757635904	snp	G/T	1.68097e-05	0.00289906	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906074	GGGCCGCCATATGAT[G/T]TGACCTTACTCAACT	1107
rs757642525	in-del	-/ATC	1.64803e-05	0.00287052	cds-indel	CHD3	GRCh38.p7	17:7895007	AGGAGGAGGAGGATG[-/ATC]ATCACATGGAGTACT	1107
rs757648980	snp	A/C	1.66902e-05	0.00288874	missense, synonymous-codon	CHD3	GRCh38.p7	17:7910893	CGGGGTACGGGGCGG[A/C]CTTCAGCGCCGCACC	1107
rs757665317	in-del	-/C	1.65151e-05	0.00287355	intron-variant	CHD3	GRCh38.p7	17:7900240	GCTGTGGGTCGGTCA[-/C]TTGTCACTAATAAGC	1107
rs757670110	snp	A/G	5.00021e-05	0.00499985	intron-variant	CHD3	GRCh38.p7	17:7898477	GATGAGGCCTCATTC[A/G]GACCCACTCTTTTTC	1107
rs757697737	snp	A/G	1.66504e-05	0.0028853	missense	CHD3	GRCh38.p7	17:7899536	GCAAGAAAGCTTTTA[A/G]GATGAAGGTAAGACC	1107
rs757727701	snp	A/T	1.64876e-05	0.00287116	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905942	GGATGCCTTCACCAC[A/T]CAGTGGCTGGTGCGG	1107
rs757733408	snp	C/G	1.6483e-05	0.00287076	intron-variant	CHD3	GRCh38.p7	17:7908366	GTGCAGTCTGCAAAA[C/G]CCTGTTACCTCTTCT	1107
rs757766809	snp	A/G	3.37319e-05	0.00410668	missense, synonymous-codon	CHD3	GRCh38.p7	17:7910938	CCGCCGCAGGCGCCA[A/G]TTACAGCCAGATGCC	1107
rs757799585	snp	C/T	1.65842e-05	0.00287955	intron-variant	CHD3	GRCh38.p7	17:7898491	CAGACCCACTCTTTT[C/T]CCAGAGAACTAATTA	1107
rs757816528	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7911088	CCTTGGTGGTATCCG[G/T]TGTTTTATGGGATAG	1107
rs757832075	snp	G/T	1.67424e-05	0.00289326	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903262	CCGCCACTTTCTCTT[G/T]CCCCTGCAGGCCTTT	1107
rs757860845	snp	C/T	3.41332e-05	0.00413103	intron-variant	CHD3	GRCh38.p7	17:7907345	CTGACCCCATTGTCC[C/T]CTTCCAGGCTGATGC	1107
rs757887437	snp	A/T	1.67708e-05	0.00289571	intron-variant	CHD3	GRCh38.p7	17:7901023	CAGGGAGCTGATCGA[A/T]CGCCCATTCTCAGAA	1107
rs757897038	snp	A/G	1.69706e-05	0.0029129	intron-variant	CHD3	GRCh38.p7	17:7894408	CCTCCACCGGGGTAT[A/G]TGACAGTCCTGGGCT	1107
rs757915205	snp	A/G	3.30077e-05	0.00406236	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910450	CCAGCTGGAGGAGTT[A/G]CTGAGCGACATGAAG	1107
rs757920522	in-del	-/GGCGGC	1.79281e-05	0.00299394	cds-indel	CHD3	GRCh38.p7	17:7893402	GTCAGCAGCTGCTGT[-/GGCGGC]GGCGGCGGCAGCGGC	1107
rs757998630	snp	C/T			missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905986	AGACTGAGAAGGAGT[C/T]TAAGTGAGTGTGGGT	1107
rs758029410	snp	C/T	1.69261e-05	0.00290908	missense, synonymous-codon	CHD3	GRCh38.p7	17:7910968	CTGCAGGGTCCTTCA[C/T]CACAGGTCAGCTGGT	1107
rs758049528	snp	A/G	3.37729e-05	0.00410918	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906094	CTTACTCAACTGATT[A/G]TCACCCTCCCTGTCA	1107
rs758060668	snp	A/G	1.66222e-05	0.00288285	intron-variant	CHD3	GRCh38.p7	17:7889151	TCTTGGCAAAAGGAT[A/G]TCAGGGCCCCAGGGT	1107
rs758076008	snp	A/T	2.03676e-05	0.00319114	intron-variant	CHD3	GRCh38.p7	17:7898634	CTTGTTTCTGGAGTG[A/T]TGGTGATCGAAGATT	1107
rs758113276	snp	C/T	1.72743e-05	0.00293885	missense	CHD3	GRCh38.p7	17:7907452	CCTGGAGAGATGGAG[C/T]CTGAACCTGGGTACC	1107
rs758150597	snp	C/T	4.81916e-05	0.00490851	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889774	CGAAAACGCAAGAAG[C/T]GTGTAAGTGTCAAGA	1107
rs758195285	snp	A/G	3.4064e-05	0.00412684	utr-variant-3-prime, synonymous-codon	CHD3	GRCh38.p7	17:7911680	CCCTCCACCTTCCCC[A/G]CCCCTTGGGCCATCA	1107
rs758200068	snp	A/C	1.68858e-05	0.00290561	intron-variant	CHD3	GRCh38.p7	17:7904038	TCCCAGGCCATCTCC[A/C]AAAGGCAGTATCCTT	1107
rs758200919	snp	A/G	1.64893e-05	0.0028713	synonymous-codon	CHD3	GRCh38.p7	17:7893818	AGGTCCAGGCCATAA[A/G]AGGCGGAGTAAGAGC	1107
rs758235961	in-del	-/TC			intron-variant	CHD3	GRCh38.p7	17:7896220	GCGACAGAGCGACAC[-/TC]TATCTCAAAAAAAAA	1107
rs758240084	snp	A/G	1.64814e-05	0.00287061	synonymous-codon	CHD3	GRCh38.p7	17:7899444	ATTCTATGTGGTGAC[A/G]TACACGGGTGACAAG	1107
rs758291284	snp	C/T	1.76256e-05	0.00296859	intron-variant	CHD3	GRCh38.p7	17:7910318	TGTGTTCTCCTCTCT[C/T]GCTCTTTTTCTGCCT	1107
rs758306421	snp	G/T	1.84232e-05	0.003035	intron-variant	CHD3	GRCh38.p7	17:7893613	TCTCACCTTCCAAAC[G/T]GCATGTCTTCACATT	1107
rs758346233	snp	C/T	1.64784e-05	0.00287035	synonymous-codon	CHD3	GRCh38.p7	17:7900870	ATACTACAAATACAT[C/T]CTGACTCGAAATTTT	1107
rs758392982	snp	A/C	9.90017e-05	0.00703499	synonymous-codon	CHD3	GRCh38.p7	17:7894192	CAGTGTCCACAGTGC[A/C]TCAGGCCGGCCTGAT	1107
rs758401528	snp	A/G	3.31312e-05	0.00406995	intron-variant	CHD3	GRCh38.p7	17:7895324	TCCTCCTCCTTGTAC[A/G]TGTCCATCCCAAAGT	1107
rs758435403	in-del	-/C			intron-variant	CHD3	GRCh38.p7	17:7895842	GGGCATGGTGGCTCA[-/C]ACCTATAATCCTAGC	1107
rs758459375	snp	A/G	4.12193e-05	0.0045396	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890611	AGCGAGATGAGTACC[A/G]GGAGAAGTCAGAGAG	1107
rs758469917	in-del	-/TTGATGGG	1.65132e-05	0.00287339	intron-variant	CHD3	GRCh38.p7	17:7900772	AGTAGGGCTTGGGGA[-/TTGATGGG]AGCGTTCCAAGTGCA	1107
rs758482317	snp	A/C			synonymous-codon	CHD3	GRCh38.p7	17:7902714	GAGGCAGGAGGCCAT[A/C]GATCGGTTTAATGGT	1107
rs758484620	snp	A/G	1.64749e-05	0.00287005	intron-variant, missense	CHD3	GRCh38.p7	17:7889016	ATGAAGGCGGCAGAC[A/G]CTGTGATCCTGTGGG	1107
rs758526965	snp	A/C	8.24029e-05	0.00641831	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7902977	CCTCCTGTCCACCCG[A/C]GCTGGGGGCCTGGGC	1107
rs758602055	snp	C/T	0.000148262	0.00860865	synonymous-codon	CHD3	GRCh38.p7	17:7897151	GGATGAGCCCCCACC[C/T]CTGGACTATGGCTCC	1107
rs758611574	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7898904	AAACTCAGGCCATAG[C/T]AGAGGGAATTGTAAT	1107
rs758631878	snp	C/T	1.88781e-05	0.00307224	synonymous-codon	CHD3	GRCh38.p7	17:7903487	CACTGAAGAGCTATT[C/T]AAGGATGAAAACGAG	1107
rs758665200	snp	C/G	9.87801e-05	0.00702711	missense, intron-variant	CHD3	GRCh38.p7	17:7907625	CGACGCCAGGAGAAA[C/G]GGGGGAGGAGAAGCC	1107
rs758679821	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7890007	TTGTCAGTGTGTCCT[C/T]AGCAGCAAAGAGAAG	1107
rs758686232	snp	G/T	5.00304e-05	0.00500127	intron-variant	CHD3	GRCh38.p7	17:7894102	TCACTGACGGCCACG[G/T]GGCTATGGGCAGTAT	1107
rs758691073	snp	C/G	1.64749e-05	0.00287005	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895509	GTGGGTAGGACTATC[C/G]TACTGGCACTGCTCC	1107
rs758705237	snp	C/G	1.64846e-05	0.0028709	intron-variant	CHD3	GRCh38.p7	17:7911451	GATCTTTCCTTACCC[C/G]TTTCCCAAACAGCCG	1107
rs758780012	snp	A/C	0.000148311	0.00861007	synonymous-codon	CHD3	GRCh38.p7	17:7899964	CATTGATCAGGCAGC[A/C]CTTGGTTCCATCCGC	1107
rs758805608	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7897427	CTGCTGTAGCTCCAG[A/C]CTTTCTGGCCTTGTT	1107
rs758844821	snp	A/C	1.66685e-05	0.00288686	missense	CHD3	GRCh38.p7	17:7894589	GGGCTCCAGAGGGCA[A/C]ATGGAGCTGCCCTCA	1107
rs758866327	snp	C/T	0.00177148	0.0297086	missense, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884999	CGGGGCCGCGACCGC[C/T]ACAGCCCCCCCGGCT	1107
rs758879746	snp	A/G	1.65422e-05	0.0028759	intron-variant	CHD3	GRCh38.p7	17:7907042	ACCTGGTAATCAGAA[A/G]TCAGGATGGTGGGAG	1107
rs758906476	snp	A/G	1.65968e-05	0.00288065	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910858	CCAGGCCTACCCGCC[A/G]GGTCCCTACGCTACA	1107
rs758932765	snp	C/T	1.8619e-05	0.00305109	missense	CHD3	GRCh38.p7	17:7893420	CGGCGGCAGCGGCAG[C/T]AGCAGCAGCAGCTGT	1107
rs758935499	snp	G/T	2.33795e-05	0.00341895	intron-variant	CHD3	GRCh38.p7	17:7890766	ATTAGGGAATGAGAG[G/T]GAGAAATCTGCATTA	1107
rs758970848	snp	C/T	1.64933e-05	0.00287165	intron-variant	CHD3	GRCh38.p7	17:7900263	TAATAAGCCCATTTT[C/T]CTGCCTTGCCTTGCC	1107
rs758983872	snp	A/G	1.66283e-05	0.00288338	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7907671	ACACAGGGAGAGGCC[A/G]GAGGGGGAAACAGGG	1107
rs759008422	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7890330	GCTACACAGGAGGCT[A/G]AGGCAGGAGAATCGC	1107
rs759025534	in-del	-/T			intron-variant	CHD3	GRCh38.p7	17:7901504	TTCCTCCTGTAAGAG[-/T]TTTTTTTTTTTTTTT	1107
rs759045536	snp	A/G	1.64792e-05	0.00287042	missense	CHD3	GRCh38.p7	17:7899071	GGAGGCACCCTGCAC[A/G]TGTATCAGTTGGAAG	1107
rs759097722	in-del	-/AGA	1.69827e-05	0.00291394	splice-acceptor-variant, cds-indel	CHD3	GRCh38.p7	17:7907892	CCTGTCTGTCCTAGC[-/AGA]AGATGTAAAAGGTGA	1107
rs759105006	snp	A/G	1.66799e-05	0.00288785	intron-variant	CHD3	GRCh38.p7	17:7910809	TTCCTCTCACAGACT[A/G]TGAACTAACTCCAAC	1107
rs759152846	in-del	-/A	0.000138591	0.00832322	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904131	TTCGTCTAATAGGTG[-/A]AGACTGGACTTCAGA	1107
rs759166950	snp	C/T	1.67438e-05	0.00289338	intron-variant	CHD3	GRCh38.p7	17:7902587	CTCATTATTGCAGAC[C/T]CCATCCTTTTCTCTT	1107
rs759171916	snp	A/G	1.95762e-05	0.00312853	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906305	CTGGTGGAAAGGATG[A/G]AGAGCTGACTGATGG	1107
rs759179869	snp	C/T	1.66513e-05	0.00288537	missense	CHD3	GRCh38.p7	17:7907911	GATGTAAAAGGTGAC[C/T]GGGAGCTTCGACCAG	1107
rs759192548	snp	C/T	1.64999e-05	0.00287222	intron-variant	CHD3	GRCh38.p7	17:7907096	AGGGCGGGAGAATCT[C/T]TGTCTTTATCACTGT	1107
rs759218196	snp	C/T	1.65206e-05	0.00287403	intron-variant	CHD3	GRCh38.p7	17:7900434	GTTCCCTAAGGGTAG[C/T]TGGCAGAGATGAGAG	1107
rs759255138	snp	C/T			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883118	TGTATGAGAAAGCTA[C/T]TTTGGGACTCCTTTC	1107
rs759272516	snp	C/T	1.65509e-05	0.00287666	intron-variant	CHD3	GRCh38.p7	17:7899240	AGGGGACCGCCTGGA[C/T]TGGGGAAGTGGGGAG	1107
rs759303159	snp	C/T	1.64751e-05	0.00287007	missense	CHD3	GRCh38.p7	17:7897194	GGGAAGAGCGACAAG[C/T]GTAAAGTGAAAGACC	1107
rs759308763	snp	C/T	1.67391e-05	0.00289297	intron-variant	CHD3	GRCh38.p7	17:7894094	AGTCTGCCTCACTGA[C/T]GGCCACGGGGCTATG	1107
rs759359903	snp	C/T	1.64743e-05	0.00287	intron-variant	CHD3	GRCh38.p7	17:7908690	GTTCCTTTTCCTTCA[C/T]TGGTAGCCATGGCTA	1107
rs759396604	snp	A/G	4.96192e-05	0.00498067	missense	CHD3	GRCh38.p7	17:7894133	GTTTTTCAGAGCGAC[A/G]AAGGTCCTGAACCAG	1107
rs759400411	snp	A/G			utr-variant-3-prime	CHD3	GRCh38.p7	17:7912183	AGCCTCAGAATAAAG[A/G]TGCCGTTCACTGGCT	1107
rs759428491	snp	C/T	1.65154e-05	0.00287358	intron-variant	CHD3	GRCh38.p7	17:7900245	GGGTCGGTCACTTGT[C/T]ACTAATAAGCCCATT	1107
rs759538249	snp	C/T	0.000131789	0.00811648	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905074	GAGAGCCCTCCCTGA[C/T]CACTGGGCCCTTTCC	1107
rs759542084	snp	C/G/T	0.000153934	0.0087719	intron-variant	CHD3	GRCh38.p7	17:7907886	CTTTGACCTGTCTGT[C/G/T]CTAGCAGAAGATGTA	1107
rs759558717	snp	A/G	0.000266845	0.0115478	synonymous-codon, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884911	GGAGGAGGAGGAGGA[A/G]GTGGAGGCGGCCGAC	1107
rs759592183	snp	A/T	1.65004e-05	0.00287227	missense	CHD3	GRCh38.p7	17:7900971	GCTGCAACCATCCAT[A/T]CCTTTTTCCCGTGGC	1107
rs759598225	snp	A/G	0.00022275	0.0105511	missense	CHD3	GRCh38.p7	17:7907390	CATCACTTGGGGAGC[A/G]GCTGGAGCCAAGGAA	1107
rs759656500	snp	G/T	1.67203e-05	0.00289134	intron-variant	CHD3	GRCh38.p7	17:7898147	ATTCTGACGATGAGG[G/T]CATGAAAGCCAAAAC	1107
rs759669078	snp	A/C	1.70866e-05	0.00292284	intron-variant	CHD3	GRCh38.p7	17:7894399	TTCCTTATCCCTCCA[A/C]CGGGGTATATGACAG	1107
rs759674098	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7907550	TCCCTCTTCTGGGGT[C/T]AGGGGATGAGGGTAA	1107
rs759725136	snp	C/T	1.66807e-05	0.00288792	intron-variant	CHD3	GRCh38.p7	17:7910358	CATCTGATGCCTCTC[C/T]TTTCCTGGCTCCATC	1107
rs759730647	snp	A/T	9.19972e-05	0.0067816	intron-variant	CHD3	GRCh38.p7	17:7893597	CTTCCAACAACTGTC[A/T]TCTCACCTTCCAAAC	1107
rs759732280	snp	G/T	1.6492e-05	0.00287154	missense	CHD3	GRCh38.p7	17:7891062	CTTCAGCCAGTTCAT[G/T]AGGTGCGGTAAGACT	1107
rs759738955	in-del	-/CCGCCGCCG	0.000292099	0.0120816	cds-indel, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885026	GGCTGCCACCTCTTC[-/CCGCCGCCG]CCGCCGCCGCCGCCA	1107
rs759745774	snp	A/G	1.67385e-05	0.00289292	intron-variant	CHD3	GRCh38.p7	17:7897952	CTCCTGCTCCTCCCC[A/G]TGGCCTCCTGCCCCA	1107
rs759766418	snp	A/T	2.17644e-05	0.00329875	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889675	AAAGATAAGGATGAC[A/T]TTCGGCTGCTGCCGT	1107
rs759803691	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7892008	ACTTCTTCAATCCTC[A/C]ATTTCCTCTTCTATA	1107
rs759864597	snp	C/G	1.64732e-05	0.0028699	intron-variant, missense	CHD3	GRCh38.p7	17:7889035	TGATCCTGTGGGCAA[C/G]AAGTAAAAATGACCA	1107
rs759891970	snp	C/T	0.000165022	0.00908206	synonymous-codon	CHD3	GRCh38.p7	17:7903973	GGTGGCACAGTACGT[C/T]GTGCGGGAAGAAGAC	1107
rs759896915	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	CHD3	GRCh38.p7	17:7895042	CGTATGCAAGGACGG[C/T]GGGGAGCTCCTGTGC	1107
rs759930109	snp	G/T	1.65957e-05	0.00288055	synonymous-codon, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906643	CCCTCGGGAGGGACT[G/T]AGTCGCCAGCAGGTG	1107
rs759954444	snp	A/G	1.64933e-05	0.00287165	intron-variant	CHD3	GRCh38.p7	17:7889117	TAATTATCCGAGGAA[A/G]TGTAAATAGAGGCCT	1107
rs759960517	snp	C/G	1.79496e-05	0.00299574	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904128	CTTCTTCGTCTAATA[C/G]GTGAGACTGGACTTC	1107
rs759988428	snp	A/G	2.06132e-05	0.00321033	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911643	GCCGACCCCCAGCTC[A/G]AGCGCTGGGGCCTGC	1107
rs760020057	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7901402	CCTTAGCTGTCTTTA[C/T]ATCTGCTTCCTCTTC	1107
rs760046263	snp	A/T	1.71761e-05	0.00293049	intron-variant	CHD3	GRCh38.p7	17:7908031	ACAGGTTGGGGAGAC[A/T]CTCGCTGCTTTCTGC	1107
rs760173651	snp	C/T	1.68332e-05	0.00290109	synonymous-codon, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906667	GCAGGTGTTGACCCG[C/T]ATTGGAGTCATGTCT	1107
rs760186143	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7891442	TGTTCCTGAACTTCC[G/T]TAGCTCACTTAGCAG	1107
rs760227437	snp	C/T	1.64879e-05	0.00287118	synonymous-codon	CHD3	GRCh38.p7	17:7899381	GGTGAGTGCCCCACT[C/T]TCTACCATCATTAAC	1107
rs760240203	snp	A/C	1.65255e-05	0.00287445	intron-variant	CHD3	GRCh38.p7	17:7906847	GGAGCTGACACCTAA[A/C]CCTCCCACCCTGCCA	1107
rs760265800	snp	A/G	1.65996e-05	0.00288089	synonymous-codon	CHD3	GRCh38.p7	17:7907916	AAAAGGTGACCGGGA[A/G]CTTCGACCAGGGCCT	1107
rs760284231	snp	C/T	1.6483e-05	0.00287076	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903004	GGGCATCAATCTGGC[C/T]ACTGCTGACACTGTC	1107
rs760313599	snp	A/G	1.65581e-05	0.00287728	intron-variant	CHD3	GRCh38.p7	17:7899250	CTGGACTGGGGAAGT[A/G]GGGAGGGGGAAGATA	1107
rs760336507	snp	C/G	1.64787e-05	0.00287038	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905191	TGTTCCTGACTCTAC[C/G]TCACCTCTTCCCGTT	1107
rs760435641	in-del	-/C	1.75517e-05	0.00296236	intron-variant	CHD3	GRCh38.p7	17:7908068	AGGGGATCTGCTCAT[-/C]CTCATGGGGTTTCTC	1107
rs760436956	snp	A/G	4.21781e-05	0.00459209	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890665	GACCGGGTCGGAAAC[A/G]AAGAAGGAAGCACCG	1107
rs760439208	snp	A/C/G	4.98677e-05	0.00499317	missense	CHD3	GRCh38.p7	17:7894254	GCCGGCCAGGAAGGA[A/C/G]GAAGAAGAAGGGTAA	1107
rs760441335	in-del	-/CCAGAGACAGGGATCCGTGAGGGCCAAGG	1.68755e-05	0.00290473	intron-variant	CHD3	GRCh38.p7	17:7893981	CTGGGGGCCAAGGAT[lengthTooLong]ATCCAGAGACAGGGA	1107
rs760495283	snp	C/T			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886188	CAGCTTGACCATCAC[C/T]CAGCACCCGTCCCCC	1107
rs760496386	in-del	-/T	1.64765e-05	0.00287019	intron-variant, frameshift-variant	CHD3	GRCh38.p7	17:7889001	CTTTCTCCTGTGTGA[-/T]TGAAGGCGGCAGACA	1107
rs760529265	snp	A/G	4.05137e-05	0.00450058	intron-variant	CHD3	GRCh38.p7	17:7890787	ATCTGCATTAAAGAC[A/G]GGCATGAGGAGGGGA	1107
rs760550586	snp	C/G			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7887355	TAAAATAATAGCAGT[C/G]GTGTTGGTGGGGGAA	1107
rs760578765	snp	A/G	1.64749e-05	0.00287005	synonymous-codon	CHD3	GRCh38.p7	17:7897193	TGGGAAGAGCGACAA[A/G]CGTAAAGTGAAAGAC	1107
rs760585202	snp	C/T			synonymous-codon	CHD3	GRCh38.p7	17:7908487	CAGAAGACATGACTA[C/T]TGGCTTCTGGCTGGG	1107
rs760635105	snp	C/G	1.65004e-05	0.00287227	missense	CHD3	GRCh38.p7	17:7894173	AATCAGACCTGGACA[C/G]TGGCAGTGTCCACAG	1107
rs760647788	snp	C/G			missense, intron-variant	CHD3	GRCh38.p7	17:7907663	GGACAGGAACACAGG[C/G]AGAGGCCGGAGGGGG	1107
rs760658478	snp	A/C	1.64868e-05	0.00287109	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905808	GAAAGGACAAGACCT[A/C]AGAACCCTAGACATT	1107
rs760728006	snp	A/C	1.72716e-05	0.00293862	missense	CHD3	GRCh38.p7	17:7898591	CCAGTTCTCCCACTA[A/C]TGATGTGAGTCCTCT	1107
rs760765054	snp	A/G	3.32751e-05	0.00407878	intron-variant	CHD3	GRCh38.p7	17:7910823	TATGAACTAACTCCA[A/G]CTTCTGCTTCCTCTC	1107
rs760785681	snp	C/T	8.53774e-05	0.0065331	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906119	CTGTCATACAATACT[C/T]CCTGGCTCGATTTCC	1107
rs760813916	snp	A/G	1.7161e-05	0.0029292	synonymous-codon	CHD3	GRCh38.p7	17:7893388	CAACCCCTTCAAGGG[A/G]TCAGCAGCTGCTGTG	1107
rs760820477	in-del	-/GAAT	3.35582e-05	0.00409609	intron-variant	CHD3	GRCh38.p7	17:7894072	CCTGGGGAGGGCGTA[-/GAAT]GAATGAAGTCTGCCT	1107
rs760868360	snp	A/G	1.64822e-05	0.00287068	missense, synonymous-codon	CHD3	GRCh38.p7	17:7911494	CTCCAGTGCTTGTGA[A/G]GAAGGAGAAGGAAAT	1107
rs760873643	snp	A/G	3.32812e-05	0.00407915	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906031	TTGGACGCAAGGGGA[A/G]GAGCTTTGGGTGTTC	1107
rs760879469	snp	A/G	2.66301e-05	0.00364888	intron-variant	CHD3	GRCh38.p7	17:7907554	TCTTCTGGGGTCAGG[A/G]GATGAGGGTAACATC	1107
rs760888252	snp	C/G	1.70258e-05	0.00291764	intron-variant	CHD3	GRCh38.p7	17:7894402	CTTATCCCTCCACCG[C/G]GGTATATGACAGTCC	1107
rs760900083	snp	A/C	2.03913e-05	0.003193	missense	CHD3	GRCh38.p7	17:7893471	CTGTCTCGTCGGCCA[A/C]CCCCATAGCACCCTC	1107
rs760907453	snp	A/T			missense	CHD3	GRCh38.p7	17:7900592	GAGGAGTTTGCTGAC[A/T]TATCCAAAGAGGACC	1107
rs760933320	snp	C/T	3.37564e-05	0.00410817	missense	CHD3	GRCh38.p7	17:7908491	AGACATGACTATTGG[C/T]TTCTGGCTGGGATTG	1107
rs760955613	snp	G/T	4.9498e-05	0.00497459	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903412	GGTTGTGCGGCCTGG[G/T]CTGGGCTCCAAGGCA	1107
rs760956302	snp	A/G	1.70834e-05	0.00292257	intron-variant	CHD3	GRCh38.p7	17:7911022	CACTCCTCCTTTGCC[A/G]AACTTTATTTCTGCT	1107
rs760985024	snp	G/T	1.66899e-05	0.00288871	intron-variant	CHD3	GRCh38.p7	17:7901012	GATACACAGAGCAGG[G/T]AGCTGATCGAACGCC	1107
rs761018482	snp	G/T	4.95364e-05	0.00497652	intron-variant	CHD3	GRCh38.p7	17:7893794	TCTTCTCACCCCGAC[G/T]CCTCATTCAGGTCCA	1107
rs761036641	snp	C/G	1.65507e-05	0.00287664	intron-variant	CHD3	GRCh38.p7	17:7910399	CCTGTCTTTCTCTTG[C/G]CCTTCTTTCTCTGTG	1107
rs761069303	snp	A/G	1.88931e-05	0.00307346	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889712	TGGGTGTGAAGAAGA[A/G]AAAACGAGGACCCAA	1107
rs761074979	snp	A/G	1.97101e-05	0.00313921	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904149	ACTGGACTTCAGAGA[A/G]AAACGTAGGCACAGA	1107
rs761108313	snp	A/G	4.9498e-05	0.00497459	intron-variant	CHD3	GRCh38.p7	17:7889122	ATCCGAGGAAATGTA[A/G]ATAGAGGCCTCCCTC	1107
rs761177207	snp	C/T	3.46075e-05	0.00415963	intron-variant	CHD3	GRCh38.p7	17:7901234	CTCCTCCTCTCTCCT[C/T]CCTTTTCAGGAGTCC	1107
rs761194892	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895419	AGTGCCAGCCCCTCA[A/G]CAGGCAGATGGAAAT	1107
rs761220038	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7889781	GCAAGAAGCGTGTAA[A/G]TGTCAAGAATTCCTA	1107
rs761244813	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7902268	CTCTACTTAAAATAC[A/G]AAAATTAGCTGGGCG	1107
rs761248064	snp	A/G	1.71085e-05	0.00292471	missense	CHD3	GRCh38.p7	17:7907402	AGCGGCTGGAGCCAA[A/G]GAAGATTCCTCTAGA	1107
rs761249359	snp	C/T			utr-variant-3-prime, synonymous-codon	CHD3	GRCh38.p7	17:7911599	GACTGGATCCCAGGC[C/T]TGCCCTTCACCCAGG	1107
rs761253294	snp	A/G	1.68806e-05	0.00290517	intron-variant	CHD3	GRCh38.p7	17:7898448	TTCAGAAAAGAAAGC[A/G]TAGGACTCCCAAGGA	1107
rs761263308	snp	A/G	1.64746e-05	0.00287002	missense	CHD3	GRCh38.p7	17:7893856	TGCCTGATGGACGCA[A/G]GAAGCTTCGGGGAAA	1107
rs761312778	snp	C/T	1.66291e-05	0.00288345	intron-variant	CHD3	GRCh38.p7	17:7895314	CCTCTTTCTTTCCTC[C/T]TCCTTGTACGTGTCC	1107
rs761330791	snp	G/T	0.000390854	0.0139741	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904167	ACGTAGGCACAGACA[G/T]TACTGGTAAACACAG	1107
rs761368176	snp	A/G	1.68292e-05	0.00290075	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904609	CAATGATGCTGCTCA[A/G]GAAGACCAAGGTGAG	1107
rs761382967	snp	G/T	1.64741e-05	0.00286998	missense	CHD3	GRCh38.p7	17:7893878	TCGGGGAAAGAAAAT[G/T]GCACCACTCAAAATA	1107
rs761418478	snp	C/T	3.2994e-05	0.00406152	intron-variant	CHD3	GRCh38.p7	17:7906863	CCTCCCACCCTGCCA[C/T]CCCAGGTGCAGGAGT	1107
rs761445019	snp	C/T	1.70446e-05	0.00291925	intron-variant	CHD3	GRCh38.p7	17:7899583	CTGAGACCCTCAAAG[C/T]TGTCACTTCTTTTTC	1107
rs761473307	snp	C/G	2.11218e-05	0.00324968	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889758	CAAGCCAGGAAAACC[C/G]CGAAAACGCAAGAAG	1107
rs761482758	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7891002	GGAGGATGTGGAGCA[C/T]GTGTTCTCTGAGGAG	1107
rs761557613	snp	C/T	1.65288e-05	0.00287474	missense, intron-variant	CHD3	GRCh38.p7	17:7895447	AATCCAGATGTCCCA[C/T]CCCCCCGTCCTCTTC	1107
rs761640005	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7909744	CCCTCACATGTGTTT[A/C]ACCCCATAAGGCAGA	1107
rs761662355	snp	A/G	3.29647e-05	0.00405971	synonymous-codon	CHD3	GRCh38.p7	17:7899423	GTTCCAGATGTGGGC[A/G]CCCAAATTCTATGTG	1107
rs761678811	snp	C/G/T	8.57605e-05	0.00654784	intron-variant	CHD3	GRCh38.p7	17:7894393	CCCTGCTTCCTTATC[C/G/T]CTCCACCGGGGTATA	1107
rs761698809	in-del	-/CCTCCTGCTCCTCCCCATGG	3.37712e-05	0.00410907	intron-variant	CHD3	GRCh38.p7	17:7897935	TCTGTGCAATATTTT[-/CCTCCTGCTCCTCCCCATGG]CCTCCTGCTCCTCCC	1107
rs761715430	in-del	-/G	3.36086e-05	0.00409917	intron-variant	CHD3	GRCh38.p7	17:7894065	CCAAAGGCCTGGGGA[-/G]GGGCGTAGAATGAAG	1107
rs761767060	snp	C/T	8.34174e-05	0.00645769	intron-variant	CHD3	GRCh38.p7	17:7898139	TTCAAGGGATTCTGA[C/T]GATGAGGGCATGAAA	1107
rs761816620	snp	A/C	1.64738e-05	0.00286995	missense	CHD3	GRCh38.p7	17:7908737	ATCCAGAATGATGCT[A/C]AATTTGCCATTATCA	1107
rs761818478	snp	C/T	1.72674e-05	0.00293827	intron-variant	CHD3	GRCh38.p7	17:7908036	TTGGGGAGACTCTCG[C/T]TGCTTTCTGCTCCTC	1107
rs761888565	snp	C/T	1.77244e-05	0.00297689	utr-variant-3-prime, synonymous-codon	CHD3	GRCh38.p7	17:7911623	ACCCAGGCCCCGTCC[C/T]CGAGGCCGACCCCCA	1107
rs761921252	snp	A/G	1.74537e-05	0.00295407	missense	CHD3	GRCh38.p7	17:7893528	CTGCTGCTGATATCC[A/G]GCCCCCACCCATCCG	1107
rs761936762	snp	C/G	1.67396e-05	0.00289301	intron-variant	CHD3	GRCh38.p7	17:7903813	GTTCCCGTTTGTTTT[C/G]CCTCTCACCAGGGGA	1107
rs761949187	snp	C/G	0.000372787	0.0136475	missense, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884941	CGAGGACGATGAGGA[C/G]GACGACGACGAGGGA	1107
rs761963029	snp	C/T	0.0164236	0.0891182	missense	CHD3	GRCh38.p7	17:7893485	ACCCCCATAGCACCC[C/T]CCGGACCCCCCGCCC	1107
rs762010724	snp	C/T	0.000114371	0.00756123	synonymous-codon	CHD3	GRCh38.p7	17:7909145	TCTGTGCCCTCAGCT[C/T]CTGGAGCAGGCGCTG	1107
rs762026574	snp	C/T	8.35541e-05	0.00646297	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903454	CAAGCAGGAGCTTGA[C/T]GACATTCTCAAATTT	1107
rs762026638	snp	A/G	1.84296e-05	0.00303553	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906230	GCGTTGAAGCAAGGA[A/G]CCTCTCCTGGGCTGT	1107
rs762092534	snp	C/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904322	ATGTATGCAGAGCCA[C/T]GAAGCTGCAGGAGTG	1107
rs762103047	snp	C/G	0.000148744	0.00862265	intron-variant	CHD3	GRCh38.p7	17:7900445	GTAGTTGGCAGAGAT[C/G]AGAGGTGGAGCAGAT	1107
rs762116258	snp	G/T	1.71917e-05	0.00293182	missense	CHD3	GRCh38.p7	17:7907441	TGCCAGGGGTGCCTG[G/T]AGAGATGGAGCCTGA	1107
rs762127995	snp	A/G	3.66119e-05	0.00427839	intron-variant	CHD3	GRCh38.p7	17:7898608	GATGTGAGTCCTCTC[A/G]GTTGTCATTTCTTGT	1107
rs762170434	snp	C/T	0.000550598	0.016583	intron-variant	CHD3	GRCh38.p7	17:7907570	GATGAGGGTAACATC[C/T]TCCCTTCCTATCCCC	1107
rs762260094	snp	A/G	1.65663e-05	0.002878	missense	CHD3	GRCh38.p7	17:7910517	ATACCCCCCATCGCA[A/G]CCCGCCTTCAGATGT	1107
rs762275696	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7891535	GAGCTTCAGTGGCTC[C/G]TGAAGAAAAGTAGAG	1107
rs762310750	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7894855	CCTGTCTTTGCCTGT[A/G]TCTTCCAGTTTCATT	1107
rs762324024	snp	A/T	1.65449e-05	0.00287614	missense	CHD3	GRCh38.p7	17:7899029	ACCGTGAAATATGAG[A/T]CTCAGCCACGGTTTA	1107
rs762335133	in-del	-/CT	1.79764e-05	0.00299798	intron-variant	CHD3	GRCh38.p7	17:7898603	CTAATGATGTGAGTC[-/CT]CTCAGTTGTCATTTC	1107
rs762341187	snp	A/G	3.31395e-05	0.00407046	missense	CHD3	GRCh38.p7	17:7894128	AGTATGTTTTTCAGA[A/G]CGACGAAGGTCCTGA	1107
rs762376795	snp	C/T	0.000182973	0.00956312	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890642	TGGGGGCAGTGAATA[C/T]GGAACCGGACCGGGT	1107
rs762403703	snp	A/G			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888204	CCCCCCTGCACACAC[A/G]CACACAGTCCTAGAG	1107
rs762425529	snp	C/T	7.67548e-05	0.00619447	intron-variant	CHD3	GRCh38.p7	17:7890529	AACAGTTTCTGGCAA[C/T]GGTAGGGATGAATAA	1107
rs762444657	snp	C/T			intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906486	TCAGTCATCCTCGCG[C/T]CTCCCTCACTGCCCT	1107
rs762458927	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7889540	CAGTGAAGGGAGGCA[A/G]GGCTTGGAGGAGTTA	1107
rs762461286	snp	G/T			intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903161	AAATAAATCTCTTCT[G/T]GGAGGAGAGAAGGCC	1107
rs762502222	snp	A/G			downstream-variant-500B	CHD3	GRCh38.p7	17:7912803	AGTTTTTGGGGGGAG[A/G]GATAAGAAAGGTTGT	1107
rs762514958	snp	A/C	3.58777e-05	0.00423527	intron-variant	CHD3	GRCh38.p7	17:7901423	CTTCCTCTTCCCTCT[A/C]CTCATCCTCCAGACT	1107
rs762569353	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7907585	CTCCCTTCCTATCCC[C/T]TACCCCCTCCCACAG	1107
rs762660322	snp	C/T	1.65836e-05	0.0028795	missense, synonymous-codon	CHD3	GRCh38.p7	17:7910530	CAGCCCGCCTTCAGA[C/T]GTCCGAGCGCAGCAT	1107
rs762675472	snp	C/T	1.70592e-05	0.0029205	intron-variant	CHD3	GRCh38.p7	17:7911011	CCTGCTACTCACACT[C/T]CTCCTTTGCCAAACT	1107
rs762689656	snp	C/T	1.6473e-05	0.00286988	intron-variant	CHD3	GRCh38.p7	17:7894082	GGCGTAGAATGAAGT[C/T]TGCCTCACTGACGGC	1107
rs762693054	snp	C/T	1.64833e-05	0.00287078	stop-gained, downstream-variant-500B	CHD3	GRCh38.p7	17:7903353	GCGTCAGTGGAAGAG[C/T]GAATCACACAAGTGG	1107
rs762783278	snp	A/C	1.70866e-05	0.00292284	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903241	CCGGCCACTCCCCTG[A/C]CCCACCCGCCACTTT	1107
rs762794047	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7897023	GGCCTCTTCCCGGTT[C/T]CTTGTTGTCCTCTGT	1107
rs762815379	snp	C/G	3.3896e-05	0.00411666	synonymous-codon	CHD3	GRCh38.p7	17:7893349	GACCATCCTTGGGGC[C/G]AAATGGAGAGAGTTC	1107
rs762826875	snp	C/T	1.73827e-05	0.00294806	intron-variant	CHD3	GRCh38.p7	17:7908049	CGCTGCTTTCTGCTC[C/T]TCAAGGGGATCTGCT	1107
rs762876493	snp	C/G	1.64958e-05	0.00287187	missense	CHD3	GRCh38.p7	17:7907211	GGAGGAAAAGCCAGA[C/G]AAGAACAGCAGAATT	1107
rs762891655	snp	C/G	1.87285e-05	0.00306005	intron-variant	CHD3	GRCh38.p7	17:7900082	GTTGTGGACTTCCCA[C/G]TTGCCTTGGTCCTAA	1107
rs762962415	snp	A/G	3.88455e-05	0.00440695	synonymous-codon	CHD3	GRCh38.p7	17:7909187	GCAGCTGCGGCGGGC[A/G]GCCTACCTGAACCTG	1107
rs762974616	snp	A/C	3.30077e-05	0.00406236	missense	CHD3	GRCh38.p7	17:7906969	GAGCCTCCTCTCCTA[A/C]CAAAACGTCTCCCAC	1107
rs762995492	snp	C/T	1.64789e-05	0.0028704	synonymous-codon	CHD3	GRCh38.p7	17:7903946	CATGAATGAGTATCT[C/T]AGCTCCTTCAAGGTG	1107
rs763000903	in-del	-/A	1.65649e-05	0.00287788	intron-variant	CHD3	GRCh38.p7	17:7902738	AATGGTGAGGGAGAT[-/A]ACACTGGTCCCTGGT	1107
rs763021354	snp	C/T	0.000261677	0.0114355	synonymous-codon	CHD3	GRCh38.p7	17:7909325	CAAGCCGGCCAACGC[C/T]GTCCTGCACAAGGGT	1107
rs763051729	snp	C/T			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7882862	GCTCCTGAGCACCGC[C/T]GAAGATGGGTGGCCA	1107
rs763052067	snp	C/T	1.64841e-05	0.00287085	intron-variant	CHD3	GRCh38.p7	17:7889110	TGCCTGGTAATTATC[C/T]GAGGAAATGTAAATA	1107
rs763088915	snp	A/G	1.65015e-05	0.00287237	intron-variant	CHD3	GRCh38.p7	17:7900746	AGTAAGATGCAAGAC[A/G]AGCTGCCTGGAGTAG	1107
rs763099436	in-del	-/GAGGAA	2.06567e-05	0.00321371	cds-indel, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884905	GACGAGGAGGAGGAG[-/GAGGAA]GAGGAGGTGGAGGCG	1107
rs763101770	snp	A/T	1.64738e-05	0.00286995	intron-variant, missense	CHD3	GRCh38.p7	17:7889026	CAGACACTGTGATCC[A/T]GTGGGCAAGAAGTAA	1107
rs763149732	snp	C/T	1.64931e-05	0.00287163	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905203	TACCTCACCTCTTCC[C/T]GTTTTATTTTCCAGT	1107
rs763225676	snp	A/G	6.62098e-05	0.00575331	intron-variant	CHD3	GRCh38.p7	17:7907289	GGAGCGGGAGGGGAG[A/G]GGGCTTGGAGGCCAG	1107
rs763253818	snp	C/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904692	TGAAGGCTGGAGCTA[C/T]TTAGAGGGAAAGAGA	1107
rs763282248	snp	A/G	3.38301e-05	0.00411265	intron-variant	CHD3	GRCh38.p7	17:7897926	CTGTTTGTGATCTGT[A/G]CAATATTTTCCTCCT	1107
rs763283640	snp	C/G	0.00198798	0.0314648	missense	CHD3	GRCh38.p7	17:7893488	CCCATAGCACCCTCC[C/G]GACCCCCCGCCCTTC	1107
rs763283692	snp	A/G	4.94246e-05	0.0049709	synonymous-codon	CHD3	GRCh38.p7	17:7895036	CTGCCGCGTATGCAA[A/G]GACGGCGGGGAGCTC	1107
rs763322475	snp	C/T	3.80539e-05	0.00436182	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906258	TGTCCTAGCCTCACA[C/T]TTACTTGACCACAAT	1107
rs763330095	in-del	-/GTT	1.66424e-05	0.0028846	intron-variant	CHD3	GRCh38.p7	17:7908543	TGCAAGAAGGAAAAG[-/GTT]CTCTCAAGCTGGCAA	1107
rs763345207	snp	C/T	0.000165377	0.00909181	intron-variant	CHD3	GRCh38.p7	17:7899232	GACCTTGAAGGGGAC[C/T]GCCTGGACTGGGGAA	1107
rs763358314	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7891598	AGGTGCAGTGGCTCA[C/T]GCCTGTAATCCAAGC	1107
rs763370028	snp	C/T	1.65266e-05	0.00287455	synonymous-codon, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906622	TGAAACCTTTGCCGA[C/T]GGGGTCCCTCGGGAG	1107
rs763375312	snp	C/T	1.75752e-05	0.00296433	missense	CHD3	GRCh38.p7	17:7893536	GATATCCAGCCCCCA[C/T]CCATCCGAAGAGCCA	1107
rs763492812	snp	C/T	4.83045e-05	0.00491426	utr-variant-3-prime, synonymous-codon	CHD3	GRCh38.p7	17:7911656	TCAAGCGCTGGGGCC[C/T]GCTGCCAGCCCTCCA	1107
rs763515243	snp	C/T	3.41012e-05	0.0041291	synonymous-codon, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906685	TGGAGTCATGTCTCT[C/T]GTCAAAAAGAAGGTA	1107
rs763537744	snp	A/G	1.64836e-05	0.0028708	synonymous-codon	CHD3	GRCh38.p7	17:7899402	CATCATTAACTGGGA[A/G]CGGGAGTTCCAGATG	1107
rs763559902	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7895232	CACATGTCCAGCTTT[C/T]CATTTCTCTGCACTC	1107
rs763610261	snp	C/G/T	0.000120145	0.00774979	intron-variant	CHD3	GRCh38.p7	17:7899592	TCAAAGCTGTCACTT[C/G/T]TTTTTCTCAGCCAGG	1107
rs763651752	snp	C/T			utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912297	AATGGTTGGGTGATA[C/T]TCCCTCAAGCCAAAG	1107
rs763667536	in-del	-/T	5.80653e-05	0.00538788	intron-variant	CHD3	GRCh38.p7	17:7908371	GTCTGCAAAACCCTG[-/T]TACCTCTTCTGTCTG	1107
rs763703157	snp	C/T	1.6528e-05	0.00287467	intron-variant	CHD3	GRCh38.p7	17:7900811	TATCATAATTGCTTC[C/T]TTTATTTATGTTTCT	1107
rs763703312	snp	C/T	2.0153e-05	0.00317428	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904153	GACTTCAGAGAGAAA[C/T]GTAGGCACAGACAGT	1107
rs763706089	snp	A/C	4.95332e-05	0.00497636	intron-variant	CHD3	GRCh38.p7	17:7893795	CTTCTCACCCCGACT[A/C]CTCATTCAGGTCCAG	1107
rs763747673	snp	C/T	4.1517e-05	0.00455596	intron-variant	CHD3	GRCh38.p7	17:7909432	CCCACCCCCTGACCC[C/T]TCTACCTGCTGAACC	1107
rs763793148	snp	C/T	9.97622e-05	0.00706195	intron-variant	CHD3	GRCh38.p7	17:7904001	GACAAGGTGAGAGGC[C/T]TTGGGGGCCAGACAT	1107
rs763798077	snp	A/G			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883551	AAGGCTGGGTAAAGG[A/G]GAGAATCAAACATGG	1107
rs763807950	snp	C/T	1.66051e-05	0.00288137	intron-variant	CHD3	GRCh38.p7	17:7902604	CATCCTTTTCTCTTG[C/T]TCTAGATGACCAAAA	1107
rs763865150	snp	C/T	1.65206e-05	0.00287403	intron-variant	CHD3	GRCh38.p7	17:7906849	AGCTGACACCTAACC[C/T]TCCCACCCTGCCACC	1107
rs763880939	snp	C/T	1.65362e-05	0.00287538	intron-variant	CHD3	GRCh38.p7	17:7890889	GGCCTGTGTGCGGCC[C/T]GGAATAGGGGCTGGA	1107
rs763883014	snp	C/T	4.94434e-05	0.00497184	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905196	CTGACTCTACCTCAC[C/T]TCTTCCCGTTTTATT	1107
rs763890842	snp	C/G	1.65734e-05	0.00287862	missense	CHD3	GRCh38.p7	17:7907921	GTGACCGGGAGCTTC[C/G]ACCAGGGCCTCGAGA	1107
rs763902812	snp	C/T	3.331e-05	0.00408092	intron-variant	CHD3	GRCh38.p7	17:7895309	TTCTGCCTCTTTCTT[C/T]CCTCCTCCTTGTACG	1107
rs763903312	snp	C/T	3.29995e-05	0.00406185	synonymous-codon	CHD3	GRCh38.p7	17:7894186	CAGTGGCAGTGTCCA[C/T]AGTGCCTCAGGCCGG	1107
rs763918158	in-del	-/CAGAGACAGGGATCCGTGAGGGCCAAGGATT	3.34219e-05	0.00408777	intron-variant	CHD3	GRCh38.p7	17:7893981	TGGGGGCCAAGGATC[lengthTooLong]CAGAGACAGGGATCC	1107
rs763973005	in-del	-/G	1.64732e-05	0.0028699	intron-variant, frameshift-variant	CHD3	GRCh38.p7	17:7889056	AAAATGACCAGCTGA[-/G]GATTTCTTTTCCTCC	1107
rs764034469	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7893965	CCTGTCTACTAAACA[C/T]CTGGGGGCCAAGGAT	1107
rs764096718	snp	A/G	1.65329e-05	0.0028751	intron-variant	CHD3	GRCh38.p7	17:7899295	GCAGAGGACTAGGGT[A/G]TACGGCCTCTAGCCT	1107
rs764149235	snp	C/T	0.00013192	0.00812049	intron-variant	CHD3	GRCh38.p7	17:7911413	ATTGTCATGAAGTGA[C/T]GTTTGAGAGTGATCT	1107
rs764152585	snp	C/T	1.6593e-05	0.00288031	intron-variant, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902904	CAGAACTACCGGGTA[C/T]AAGAAAAACCTGATC	1107
rs764168193	snp	A/G	1.66087e-05	0.00288168	missense	CHD3	GRCh38.p7	17:7910868	CCGCCGGGTCCCTAC[A/G]CTACACCTCCGGGGT	1107
rs764171230	snp	C/T	1.65334e-05	0.00287514	missense	CHD3	GRCh38.p7	17:7907014	CTGCTACCAACAGTC[C/T]CTGCACCTCTAAACC	1107
rs764213049	snp	A/G/T			intron-variant	CHD3	GRCh38.p7	17:7895698	TAGTTTCCATATGTG[A/G/T]TTCTTTTGGTCTACA	1107
rs764223458	in-del	-/CT	3.4413e-05	0.00414793	intron-variant	CHD3	GRCh38.p7	17:7910624	TAGCTCCAGTTTTCC[-/CT]GTTTGTGTTCCTCCT	1107
rs764255480	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	CHD3	GRCh38.p7	17:7908697	TTCCTTCATTGGTAG[C/T]CATGGCTATGCACGG	1107
rs764276937	in-del	-/ACTG	0.000418743	0.0144636	intron-variant	CHD3	GRCh38.p7	17:7894089	AATGAAGTCTGCCTC[-/ACTG]ACGGCCACGGGGCTA	1107
rs764282702	snp	C/T	3.43118e-05	0.00414183	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906127	CAATACTTCCTGGCT[C/T]GATTTCCTGGGGGGT	1107
rs764343442	snp	C/G/T	3.35268e-05	0.0040942	missense	CHD3	GRCh38.p7	17:7908509	CTGGCTGGGATTGTC[C/G/T]TGTATCCTTTGATAC	1107
rs764363333	snp	G/T	4.96389e-05	0.00498166	intron-variant	CHD3	GRCh38.p7	17:7910402	GTCTTTCTCTTGCCC[G/T]TCTTTCTCTGTGGCC	1107
rs764384189	snp	A/G/T	3.40363e-05	0.00412519	intron-variant	CHD3	GRCh38.p7	17:7894403	TTATCCCTCCACCGG[A/G/T]GTATATGACAGTCCT	1107
rs764385417	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7901702	TTTTAGTAGAGACGG[A/G]ATTTCACCATGTTGG	1107
rs764440892	snp	A/G	1.65581e-05	0.00287728	intron-variant	CHD3	GRCh38.p7	17:7899888	ATGGGCAATAATTAT[A/G]TTGGCAGAGGGAGGC	1107
rs764462143	snp	A/T	1.66946e-05	0.00288912	intron-variant	CHD3	GRCh38.p7	17:7901013	ATACACAGAGCAGGG[A/T]GCTGATCGAACGCCC	1107
rs764466556	snp	G/T	1.71569e-05	0.00292885	missense	CHD3	GRCh38.p7	17:7893389	AACCCCTTCAAGGGG[G/T]CAGCAGCTGCTGTGG	1107
rs764478219	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7889832	AGACCCATTCTCAGA[C/G]ACCTACATTTTCTCT	1107
rs764546545	snp	C/G	1.69867e-05	0.00291429	intron-variant	CHD3	GRCh38.p7	17:7907329	AGCCCTCTGGCTCAT[C/G]CTGACCCCATTGTCC	1107
rs764553761	snp	A/G	1.92558e-05	0.00310282	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889730	AACGAGGACCCAAGA[A/G]GCAGAAGGAGAACAA	1107
rs764562953	in-del	-/CTT			intron-variant	CHD3	GRCh38.p7	17:7891994	GGGCAAGTGACTGAA[-/CTT]CTTCAATCCTCAATT	1107
rs764580161	snp	A/G	5.06017e-05	0.00502974	intron-variant	CHD3	GRCh38.p7	17:7898450	CAGAAAAGAAAGCGT[A/G]GGACTCCCAAGGATG	1107
rs764622402	snp	A/T	1.64999e-05	0.00287222	intron-variant	CHD3	GRCh38.p7	17:7889123	TCCGAGGAAATGTAA[A/T]TAGAGGCCTCCCTCT	1107
rs764643312	snp	C/T	1.73135e-05	0.00294218	synonymous-codon	CHD3	GRCh38.p7	17:7898592	CAGTTCTCCCACTAA[C/T]GATGTGAGTCCTCTC	1107
rs764653962	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7909865	GATAGAGATTATATC[C/T]CAAAGCCCTCTAACC	1107
rs764655073	snp	A/C	1.6659e-05	0.00288604	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906035	ACGCAAGGGGAAGAG[A/C]TTTGGGTGTTCCTTT	1107
rs764659804	snp	A/G	7.23179e-05	0.0060128	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904187	GGTAAACACAGAAGG[A/G]TACCTTCTGAGACAG	1107
rs764744887	snp	G/T	0.000925085	0.0214869	missense	CHD3	GRCh38.p7	17:7907434	GATGAGGTGCCAGGG[G/T]TGCCTGGAGAGATGG	1107
rs764782731	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7901159	GTGGAAGCTGGATCC[A/G]GGCATCTGGCCTTCT	1107
rs764809850	snp	C/T	1.65671e-05	0.00287807	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910519	ACCCCCCATCGCAGC[C/T]CGCCTTCAGATGTCC	1107
rs764840474	snp	A/G	1.66255e-05	0.00288314	intron-variant	CHD3	GRCh38.p7	17:7898483	GCCTCATTCAGACCC[A/G]CTCTTTTTCCAGAGA	1107
rs764841082	snp	A/G	2.1906e-05	0.00330946	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889760	AGCCAGGAAAACCCC[A/G]AAAACGCAAGAAGCG	1107
rs764894953	snp	A/G	1.72246e-05	0.00293462	synonymous-codon	CHD3	GRCh38.p7	17:7907445	AGGGGTGCCTGGAGA[A/G]ATGGAGCCTGAACCT	1107
rs764913346	snp	C/T	1.66382e-05	0.00288424	missense	CHD3	GRCh38.p7	17:7901284	CTTATGAGGGTGGGG[C/T]ACTTATTAAGTCGTC	1107
rs764937012	in-del	-/CC			intron-variant	CHD3	GRCh38.p7	17:7894346	GACTTCTCTCTTCAA[-/CC]CTTCTCCCTCTCTCT	1107
rs765001803	snp	A/G	1.72507e-05	0.00293685	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904626	AAGACCAAGGTGAGG[A/G]CTGCCCCAGATGCAG	1107
rs765031234	snp	C/G	1.64863e-05	0.00287104	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903019	CACTGCTGACACTGT[C/G]ATCATCTTTGATTCT	1107
rs765034008	in-del	-/AAG	0.00346088	0.0414544	cds-indel	CHD3	GRCh38.p7	17:7898539	CAGCCCCGCAAGTAT[-/AAG]AAGAAGAAGAAGGAG	1107
rs765039093	snp	G/T	1.64741e-05	0.00286998	missense	CHD3	GRCh38.p7	17:7893879	CGGGGAAAGAAAATG[G/T]CACCACTCAAAATAA	1107
rs765046453	snp	C/T	1.65375e-05	0.0028755	intron-variant	CHD3	GRCh38.p7	17:7890900	GGCCTGGAATAGGGG[C/T]TGGAGGAGCACCTAC	1107
rs765101896	snp	C/T	1.65968e-05	0.00288065	intron-variant	CHD3	GRCh38.p7	17:7895319	TTCTTTCCTCCTCCT[C/T]GTACGTGTCCATCCC	1107
rs765110699	snp	A/G	8.27027e-05	0.00642997	missense	CHD3	GRCh38.p7	17:7907933	TTCGACCAGGGCCTC[A/G]AGATGAGCCACGGTC	1107
rs765119363	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7895845	CATGGTGGCTCACAC[C/G]TATAATCCTAGCACT	1107
rs765128380	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7909815	CTTCCCTTTGACCTT[C/T]GACCTTTCCTCCTAC	1107
rs765269481	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7891008	TGTGGAGCATGTGTT[C/T]TCTGAGGAGGATTAC	1107
rs765287980	snp	C/T	1.64814e-05	0.00287061	synonymous-codon	CHD3	GRCh38.p7	17:7899435	GGCACCCAAATTCTA[C/T]GTGGTGACATACACG	1107
rs765297108	snp	C/T	3.29506e-05	0.00405884	synonymous-codon	CHD3	GRCh38.p7	17:7908754	ATTTGCCATTATCAA[C/T]GAGCCATTTAAAACT	1107
rs765304702	snp	A/T	1.72847e-05	0.00293974	intron-variant	CHD3	GRCh38.p7	17:7908040	GGAGACTCTCGCTGC[A/T]TTCTGCTCCTCAAGG	1107
rs765306650	snp	A/G	1.7251e-05	0.00293687	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906703	CAAAAAGAAGGTATC[A/G]GTCTTCCTGTCACCC	1107
rs765336355	snp	C/T	1.64738e-05	0.00286995	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905089	CCACTGGGCCCTTTC[C/T]ACCCCCACAGACAAC	1107
rs765364535	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7901440	TCATCCTCCAGACTT[C/T]AATTTCTTACGGTCT	1107
rs765417103	snp	C/T	1.76911e-05	0.0029741	missense	CHD3	GRCh38.p7	17:7909156	AGCTCCTGGAGCAGG[C/T]GCTGGTGATTGAGGA	1107
rs765420961	snp	C/T	1.67153e-05	0.00289091	intron-variant	CHD3	GRCh38.p7	17:7903814	TTCCCGTTTGTTTTC[C/T]CTCTCACCAGGGGAG	1107
rs765425012	snp	A/G	1.65051e-05	0.00287267	intron-variant	CHD3	GRCh38.p7	17:7900250	GGTCACTTGTCACTA[A/G]TAAGCCCATTTTCCT	1107
rs765491759	snp	A/T	1.64906e-05	0.00287142	intron-variant	CHD3	GRCh38.p7	17:7907115	CTTTATCACTGTGCC[A/T]TCCCCTGCAGCTACT	1107
rs765515173	snp	C/T	0.000146751	0.0085647	intron-variant	CHD3	GRCh38.p7	17:7907579	AACATCCTCCCTTCC[C/T]ATCCCCTACCCCCTC	1107
rs765520216	snp	C/G	1.65051e-05	0.00287267	synonymous-codon	CHD3	GRCh38.p7	17:7899040	TGAGACTCAGCCACG[C/G]TTTATCACAGCCACT	1107
rs765531902	snp	C/T	5.63026e-05	0.00530548	missense	CHD3	GRCh38.p7	17:7893408	CAGCTGCTGTGGCGG[C/T]GGCAGCGGCAGCAGC	1107
rs765541522	snp	C/T	0.000430942	0.0146726	synonymous-codon, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884950	TGAGGAGGACGACGA[C/T]GAGGGAGTACTCGGG	1107
rs765578621	snp	A/C/G/T	6.17093e-05	0.00555444	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890653	AATATGGAACCGGAC[A/C/G/T]GGGTCGGAAACGAAG	1107
rs765598210	snp	C/T	3.40866e-05	0.00412822	intron-variant	CHD3	GRCh38.p7	17:7894904	GTCTGTGTGTCTATC[C/T]TTGGCCCCCTAGGAG	1107
rs765614498	snp	C/T	1.88404e-05	0.00306917	intron-variant	CHD3	GRCh38.p7	17:7898616	TCCTCTCAGTTGTCA[C/T]TTCTTGTTTCTGGAG	1107
rs765617826	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7911134	TCCCCCCACCCATCC[A/C]TTTCTTAACCCCTCT	1107
rs765631726	snp	A/G	3.37103e-05	0.00410537	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906086	GATGTGACCTTACTC[A/G]ACTGATTATCACCCT	1107
rs765695650	snp	A/G	1.64871e-05	0.00287111	intron-variant	CHD3	GRCh38.p7	17:7911429	GTTTGAGAGTGATCT[A/G]GAGATTGATCTTTCC	1107
rs765701464	in-del	-/TCAATAAAGGTAGACAAGTCTCGGCAGGGAGGAA	1.64947e-05	0.00287177	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905212	CTTCCCGTTTTATTT[lengthTooLong]TCCAGTTTGCTTTAA	1107
rs765713887	snp	C/T	5.18381e-05	0.00509081	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906142	CGATTTCCTGGGGGG[C/T]GGTCTCAGCCCACTC	1107
rs765798605	snp	C/G	1.65337e-05	0.00287517	missense	CHD3	GRCh38.p7	17:7894570	CTTGATCCTGAGCTT[C/G]ACCGGGCTCCAGAGG	1107
rs765800908	snp	A/G	1.67309e-05	0.00289226	missense, downstream-variant-500B	CHD3	GRCh38.p7	17:7903455	AAGCAGGAGCTTGAC[A/G]ACATTCTCAAATTTG	1107
rs765822503	snp	C/T	1.65825e-05	0.00287941	synonymous-codon	CHD3	GRCh38.p7	17:7901300	ACTTATTAAGTCGTC[C/T]GGGAAGCTCATGCTG	1107
rs765857922	snp	C/T	1.65979e-05	0.00288074	missense	CHD3	GRCh38.p7	17:7910538	CTTCAGATGTCCGAG[C/T]GCAGCATCCTCAGCC	1107
rs765950616	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7896134	TCAGGAGGCTGAGAC[A/G]GGAGAATGGCGTGAA	1107
rs765964328	snp	C/T	0.000260817	0.0114167	missense, intron-variant	CHD3	GRCh38.p7	17:7907657	TTGGATGGACAGGAA[C/T]ACAGGGAGAGGCCGG	1107
rs765997564	snp	A/T	5.6794e-05	0.00532858	intron-variant	CHD3	GRCh38.p7	17:7890555	AATAAATGTTATTTT[A/T]ATTTCTTTCTCTTAG	1107
rs766010552	snp	C/T	1.76309e-05	0.00296903	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906163	CAGCCCACTCCACCT[C/T]CCCTCAGCCGAGCCT	1107
rs766019097	snp	A/G	4.86713e-05	0.00493288	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889775	GAAAACGCAAGAAGC[A/G]TGTAAGTGTCAAGAA	1107
rs766033254	snp	C/T	1.64895e-05	0.00287132	synonymous-codon	CHD3	GRCh38.p7	17:7899052	ACGGTTTATCACAGC[C/T]ACTGGAGGCACCCTG	1107
rs766050966	in-del	-/T	1.81543e-05	0.00301277	intron-variant	CHD3	GRCh38.p7	17:7898605	ATGATGTGAGTCCTC[-/T]TCAGTTGTCATTTCT	1107
rs766079575	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7909987	CTCTCCCCTTACATA[C/T]TAAAACCGTGATTCC	1107
rs766106062	in-del	-/GAA	9.96611e-05	0.00705837	cds-indel	CHD3	GRCh38.p7	17:7894252	AGGCCGGCCAGGAAG[-/GAA]GAAGAAGAAGGGTAA	1107
rs766181710	snp	A/G	1.6684e-05	0.00288821	intron-variant	CHD3	GRCh38.p7	17:7899857	TGTAGGTGCATGGTT[A/G]TCAGGTGGCAGCTGA	1107
rs766200886	snp	C/T	3.58963e-05	0.00423638	intron-variant	CHD3	GRCh38.p7	17:7901426	CCTCTTCCCTCTCCT[C/T]ATCCTCCAGACTTTA	1107
rs766206688	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912237	CTTGTGTTGGGAATG[-/T]TTCCCCCCTCCCTAG	1107
rs766209905	snp	A/G	4.94434e-05	0.00497184	missense	CHD3	GRCh38.p7	17:7893925	GTGGCAAGAGGAAGA[A/G]AGGAGGCTCGGTGAG	1107
rs766256801	snp	A/C/T	5.15338e-05	0.0050759	intron-variant	CHD3	GRCh38.p7	17:7897042	GTTGTCCTCTGTGAG[A/C/T]GTCAGGACTATCTCT	1107
rs766274849	snp	A/G	1.64846e-05	0.0028709	missense	CHD3	GRCh38.p7	17:7906885	TGCAGGAGTTTGAGC[A/G]CATCAATGGGCGTTG	1107
rs766382716	snp	A/G	1.66443e-05	0.00288477	synonymous-codon	CHD3	GRCh38.p7	17:7894261	AGGAAGGAAGAAGAA[A/G]AAGGGTAAGGAGTGT	1107
rs766382834	snp	C/T	1.77281e-05	0.00297721	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904639	GGACTGCCCCAGATG[C/T]AGGCAGTAAAGGGGG	1107
rs766477734	snp	A/G	1.64977e-05	0.00287203	missense	CHD3	GRCh38.p7	17:7907216	AAAAGCCAGAGAAGA[A/G]CAGCAGAATTGGGGA	1107
rs766478008	snp	C/T	1.65198e-05	0.00287395	missense	CHD3	GRCh38.p7	17:7906987	AAACGTCTCCCACCA[C/T]TCCTGAGGCTTCTGC	1107
rs766500385	snp	C/T	1.6865e-05	0.00290383	intron-variant	CHD3	GRCh38.p7	17:7897939	GTGCAATATTTTCCT[C/T]CTGCTCCTCCCCATG	1107
rs766543928	snp	A/G	1.64735e-05	0.00286993	intron-variant, synonymous-codon	CHD3	GRCh38.p7	17:7889027	AGACACTGTGATCCT[A/G]TGGGCAAGAAGTAAA	1107
rs766552141	snp	C/T	3.29717e-05	0.00406015	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905829	CCTAGACATTTGTCG[C/T]CATTGCCTCCTTGCT	1107
rs766552201	snp	C/T	1.65666e-05	0.00287802	intron-variant, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902913	CGGGTACAAGAAAAA[C/T]CTGATCCAACTCTCA	1107
rs766559164	snp	A/G			synonymous-codon	CHD3	GRCh38.p7	17:7907418	GAAGATTCCTCTAGA[A/G]GATGAGGTGCCAGGG	1107
rs766562691	snp	C/G	1.65559e-05	0.00287709	intron-variant	CHD3	GRCh38.p7	17:7907292	GCGGGAGGGGAGGGG[C/G]CTTGGAGGCCAGGTA	1107
rs766581980	snp	C/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905997	GAGTTTAAGTGAGTG[C/T]GGGTGATACAGGGCT	1107
rs766586648	snp	G/T	1.65059e-05	0.00287275	intron-variant	CHD3	GRCh38.p7	17:7900758	GACGAGCTGCCTGGA[G/T]TAGGGCTTGGGGATT	1107
rs766638046	snp	A/G	3.29886e-05	0.00406118	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905204	ACCTCACCTCTTCCC[A/G]TTTTATTTTCCAGTT	1107
rs766660828	snp	C/T	0.00171379	0.0292226	missense, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885057	CGCCGCCACCGCTGC[C/T]CCCGCCGCCGCCGCC	1107
rs766666031	snp	C/T			synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7891050	CAACTACAAAGCCTT[C/T]AGCCAGTTCATGAGG	1107
rs766690054	snp	C/T	1.6507e-05	0.00287284	missense	CHD3	GRCh38.p7	17:7894199	CACAGTGCCTCAGGC[C/T]GGCCTGATGGCCCTG	1107
rs766719282	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7891786	GAATCGCTTGAACCC[A/G]GGAGGCAAAGGTTGT	1107
rs766735970	snp	A/C/T	0.000140896	0.00839224	synonymous-codon	CHD3	GRCh38.p7	17:7893538	TATCCAGCCCCCACC[A/C/T]ATCCGAAGAGCCAAA	1107
rs766746684	snp	A/T			missense	CHD3	GRCh38.p7	17:7898079	TGAATACGAAGAACA[A/T]AAGCAAAGCTACTGG	1107
rs766748362	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7909489	CCTACCGACCTGGCA[C/G]CCCCTTGGATTTTAG	1107
rs766766793	snp	C/T			utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912434	AAGACTTCTACTACC[C/T]TCCCTCCTCAAGGCC	1107
rs766775771	snp	A/G	2.18195e-05	0.00330292	missense	CHD3	GRCh38.p7	17:7903500	TTCAAGGATGAAAAC[A/G]AGGGTGAGAACCTTT	1107
rs766825687	snp	A/G	1.64838e-05	0.00287083	synonymous-codon	CHD3	GRCh38.p7	17:7908781	AACTGAAGCCAATAA[A/G]GGGAACTTTCTGGAG	1107
rs766840603	snp	A/G	5.05063e-05	0.005025	synonymous-codon	CHD3	GRCh38.p7	17:7894919	CTTGGCCCCCTAGGA[A/G]AAGGAGGGGGTCCAG	1107
rs766848702	in-del	-/A	0.0248477	0.108657	intron-variant	CHD3	GRCh38.p7	17:7908559	TTCTCTCAAGCTGGC[-/A]AAAAAAAAAAAGATG	1107
rs766849668	snp	A/C/G	1.91826e-05	0.00309693	missense	CHD3	GRCh38.p7	17:7909207	ACCTGAACCTGTCGC[A/C/G]GGAGCCGGCGCACCC	1107
rs766856387	snp	C/T	1.6483e-05	0.00287076	synonymous-codon	CHD3	GRCh38.p7	17:7903865	TGTGATTCATTATGA[C/T]AATGAGGCCATCGCT	1107
rs766875182	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7899738	GTCGGTACTGGAAAT[A/G]TGGGCAGAGGTTTAG	1107
rs766932108	snp	A/C/T	3.92259e-05	0.00442851	missense	CHD3	GRCh38.p7	17:7893492	TAGCACCCTCCGGAC[A/C/T]CCCCGCCCTTCCACC	1107
rs766963521	snp	A/T	4.97401e-05	0.00498674	intron-variant	CHD3	GRCh38.p7	17:7900507	GGTAAGTCTGAGATC[A/T]GGGGCAAGGAACTTG	1107
rs767024629	snp	A/C	1.85407e-05	0.00304467	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911633	CGTCCCCGAGGCCGA[A/C]CCCCAGCTCAAGCGC	1107
rs767034177	snp	C/G	2.06541e-05	0.00321351	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890656	ATGGAACCGGACCGG[C/G]TCGGAAACGAAGAAG	1107
rs767040046	snp	C/T			utr-variant-3-prime	CHD3	GRCh38.p7	17:7912173	ACTGCTGTTCAGCCT[C/T]AGAATAAAGGTGCCG	1107
rs767070575	snp	A/G	6.58979e-05	0.00573974	synonymous-codon	CHD3	GRCh38.p7	17:7895045	ATGCAAGGACGGCGG[A/G]GAGCTCCTGTGCTGT	1107
rs767073236	snp	A/G			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888492	TGGTAGGGGAGGGAC[A/G]TGAACCAGAGCCCCA	1107
rs767114063	snp	C/T	1.64792e-05	0.00287042	synonymous-codon	CHD3	GRCh38.p7	17:7903877	TGACAATGAGGCCAT[C/T]GCTCGGCTGTTGGAC	1107
rs767127555	snp	C/T	6.38617e-05	0.00565038	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911646	GACCCCCAGCTCAAG[C/T]GCTGGGGCCTGCTGC	1107
rs767144411	snp	A/G	1.65515e-05	0.00287671	missense	CHD3	GRCh38.p7	17:7894941	GGGGTCCAGTGGGAG[A/G]CCAAGGAGGAAGAAG	1107
rs767153801	snp	G/T	3.32685e-05	0.00407837	intron-variant	CHD3	GRCh38.p7	17:7902761	TCCCTGGTGGGTGTG[G/T]GAGGCCTGAGAAACC	1107
rs767155506	snp	C/T	1.64773e-05	0.00287026	synonymous-codon	CHD3	GRCh38.p7	17:7899076	CACCCTGCACATGTA[C/T]CAGTTGGAAGGGCTG	1107
rs767202239	snp	A/G	0.00013242	0.00813586	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906502	CTCCCTCACTGCCCT[A/G]TACCCCTTCTGTGGC	1107
rs767233135	in-del	-/AAG	1.70723e-05	0.00292162	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904399	GTGGAAGGATTAGCA[-/AAG]AAGGAGACCCCCAGT	1107
rs767237031	snp	A/G	1.64746e-05	0.00287002	missense	CHD3	GRCh38.p7	17:7897189	ATGATGGGAAGAGCG[A/G]CAAGCGTAAAGTGAA	1107
rs767239315	snp	C/T			missense	CHD3	GRCh38.p7	17:7897210	GTAAAGTGAAAGACC[C/T]GCACTATGCTGAGAT	1107
rs767286465	in-del	-/AAT	4.98144e-05	0.00499047	intron-variant	CHD3	GRCh38.p7	17:7899879	GGCAGCTGAATGGGC[-/AAT]AATTATGTTGGCAGA	1107
rs767308697	snp	G/T	1.65307e-05	0.0028749	missense	CHD3	GRCh38.p7	17:7894137	TTCAGAGCGACGAAG[G/T]TCCTGAACCAGAGGC	1107
rs767348324	in-del	-/GTCT			utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912690	TCACACCCACTCCTG[-/GTCT]GTCCTGATCCCCTCT	1107
rs767350598	snp	A/G	2.92299e-05	0.00382284	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890575	CTTTCTCTTAGGACA[A/G]TGAGGAGGAATTTGG	1107
rs767413697	snp	A/G			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883173	TTTACCATAAACACT[A/G]GGGTACAGTTGGAAA	1107
rs767425503	snp	A/G			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904346	AGGAGTGGGGAGACC[A/G]GATTGGGCTGACGCA	1107
rs767527600	snp	A/G	1.67192e-05	0.00289125	intron-variant	CHD3	GRCh38.p7	17:7902590	ATTATTGCAGACTCC[A/G]TCCTTTTCTCTTGCT	1107
rs767548476	snp	A/C	1.64741e-05	0.00286998	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905076	GAGCCCTCCCTGACC[A/C]CTGGGCCCTTTCCAC	1107
rs767573897	snp	C/T	1.74066e-05	0.00295008	intron-variant	CHD3	GRCh38.p7	17:7908051	CTGCTTTCTGCTCCT[C/T]AAGGGGATCTGCTCA	1107
rs767600398	in-del	-/TT			intron-variant	CHD3	GRCh38.p7	17:7892497	GTTTTTTATTTCCCC[-/TT]TTTTTTTTTTTTTTT	1107
rs767602308	snp	A/C	5.15017e-05	0.00507427	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903245	CCACTCCCCTGACCC[A/C]CCCGCCACTTTCTCT	1107
rs767659654	snp	A/G	1.69063e-05	0.00290738	missense	CHD3	GRCh38.p7	17:7910922	CCCGTAGGGGCCCTG[A/G]CCGCCGCAGGCGCCA	1107
rs767665992	snp	C/T	1.70638e-05	0.00292089	intron-variant	CHD3	GRCh38.p7	17:7911013	TGCTACTCACACTCC[C/T]CCTTTGCCAAACTTT	1107
rs767688124	snp	A/G/T	3.32714e-05	0.00407858	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906026	CTGAGTTGGACGCAA[A/G/T]GGGAAGAGCTTTGGG	1107
rs767694810	snp	C/T	1.64868e-05	0.00287109	synonymous-codon	CHD3	GRCh38.p7	17:7899462	CACGGGTGACAAGGA[C/T]AGCCGGGCCATCATT	1107
rs767697819	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7907584	CCTCCCTTCCTATCC[C/G]CTACCCCCTCCCACA	1107
rs767797819	in-del	-/GCCGCCGCCACCGCT	0.000517732	0.016081	cds-indel, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885039	CCCGCCGCCGCCGCC[-/GCCGCCGCCACCGCT]GCCGCCGCCACCGCT	1107
rs767870995	snp	C/T	1.64939e-05	0.0028717	intron-variant	CHD3	GRCh38.p7	17:7889118	AATTATCCGAGGAAA[C/T]GTAAATAGAGGCCTC	1107
rs767877300	snp	C/G	1.65474e-05	0.00287636	missense	CHD3	GRCh38.p7	17:7903988	CGTGCGGGAAGAAGA[C/G]AAGGTGAGAGGCTTT	1107
rs767886788	snp	C/T	1.66701e-05	0.002887	intron-variant	CHD3	GRCh38.p7	17:7897961	CTCCCCATGGCCTCC[C/T]GCCCCACAGTGTGGA	1107
rs767952562	snp	G/T	3.30093e-05	0.00406246	synonymous-codon	CHD3	GRCh38.p7	17:7907229	GAACAGCAGAATTGG[G/T]GAGAAGATGGAGACA	1107
rs767973395	snp	G/T	3.52896e-05	0.00420042	intron-variant	CHD3	GRCh38.p7	17:7901399	TGCCCTTAGCTGTCT[G/T]TACATCTGCTTCCTC	1107
rs767975917	snp	A/C	0.000284981	0.0119335	missense	CHD3	GRCh38.p7	17:7909219	CGCAGGAGCCGGCGC[A/C]CCCCGCCATGGCCCT	1107
rs767988861	snp	A/G	1.65023e-05	0.00287244	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903325	AGTGATGATTTACCG[A/G]TTTGTGACTCGCGCG	1107
rs768028401	snp	A/G			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888329	GAGGCCTCTGGTGTT[A/G]ATTGTGGCTAATTTT	1107
rs768043554	snp	C/T	8.2659e-05	0.00642827	synonymous-codon	CHD3	GRCh38.p7	17:7900981	TCCATACCTTTTTCC[C/T]GTGGCTGCTATGGTA	1107
rs768063092	snp	A/G	1.6473e-05	0.00286988	intron-variant, missense	CHD3	GRCh38.p7	17:7889038	TCCTGTGGGCAAGAA[A/G]TAAAAATGACCAGCT	1107
rs768084092	snp	A/C	1.68783e-05	0.00290498	intron-variant	CHD3	GRCh38.p7	17:7907314	GGCCAGGTACCTGGG[A/C]GCCCTCTGGCTCATC	1107
rs768086253	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7892222	ACCCGTGTCCGCACA[A/G]GAGTTGAGCACCCCA	1107
rs768154770	snp	C/T	3.29864e-05	0.00406105	missense	CHD3	GRCh38.p7	17:7906944	AGCGCCGATTCTAAG[C/T]GCTCCTCCAGAGCCT	1107
rs768182232	snp	C/T	4.35019e-05	0.00466359	intron-variant, synonymous-codon	CHD3	GRCh38.p7	17:7909358	GGGCCGCGGCGGCCC[C/T]GCGCGGGGGAGGGCC	1107
rs768183117	snp	A/G	1.73733e-05	0.00294726	intron-variant	CHD3	GRCh38.p7	17:7900043	TCCAAGGTGAGTGAG[A/G]TTTCCAGACCTAAAA	1107
rs768217347	snp	C/T	5.16382e-05	0.00508099	intron-variant	CHD3	GRCh38.p7	17:7908034	GGTTGGGGAGACTCT[C/T]GCTGCTTTCTGCTCC	1107
rs768247041	snp	C/G/T	6.58951e-05	0.00573969	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890978	AACTCTGCTTCTGAC[C/G/T]TGGGGCCTGGAGGAT	1107
rs768274490	snp	G/T	1.69703e-05	0.00291288	intron-variant	CHD3	GRCh38.p7	17:7910985	ACAGGTCAGCTGGTG[G/T]TTTCCTACCCCCTGC	1107
rs768279168	snp	A/G	3.32674e-05	0.0040783	intron-variant	CHD3	GRCh38.p7	17:7898130	GCTTGTGGATTCAAG[A/G]GATTCTGACGATGAG	1107
rs768292706	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895425	AGCCCCTCAACAGGC[A/G]GATGGAAATCCAGAT	1107
rs768305286	in-del	-/GAA	1.64825e-05	0.00287071	cds-indel	CHD3	GRCh38.p7	17:7911492	CCCTCCAGTGCTTGT[-/GAA]GAAGGAGAAGGAAAT	1107
rs768307299	snp	A/G	8.31608e-05	0.00644775	missense	CHD3	GRCh38.p7	17:7894438	TGTCCTGCAGTGGCC[A/G]GGGAGGAGGAGGTTG	1107
rs768338780	snp	C/G/T	3.44212e-05	0.00414845	intron-variant	CHD3	GRCh38.p7	17:7910329	CTCTCGCTCTTTTTC[C/G/T]GCCTGTATCTGTCCA	1107
rs768340600	snp	A/C	1.72299e-05	0.00293508	intron-variant	CHD3	GRCh38.p7	17:7894379	TCCATCTCCCCCTGC[A/C]CTGCTTCCTTATCCC	1107
rs768427173	in-del	-/C	1.66471e-05	0.00288501	intron-variant	CHD3	GRCh38.p7	17:7895567	CTTTTCTTTCCCTCT[-/C]CCCCCATGACCTCAT	1107
rs768470689	snp	C/T	1.77074e-05	0.00297547	synonymous-codon	CHD3	GRCh38.p7	17:7908439	TGAGGAACGGGCAGC[C/T]ATTTCCTCGGGGAAA	1107
rs768510465	snp	C/G	3.25972e-05	0.00403702	intron-variant	CHD3	GRCh38.p7	17:7889648	CTTAGGTTTTCTGAT[C/G]CTTTTTGCTTCAAAG	1107
rs768583485	snp	A/G	1.6476e-05	0.00287014	intron-variant, missense	CHD3	GRCh38.p7	17:7889094	TGTTGGGGTGACAGG[A/G]TGCCTGGTAATTATC	1107
rs768604956	snp	C/T	1.64754e-05	0.00287009	synonymous-codon	CHD3	GRCh38.p7	17:7900909	GAATTCACGAGGTGG[C/T]GGGAACCAGGTGTCG	1107
rs768618853	snp	A/C	0.0812443	0.184449	missense	CHD3	GRCh38.p7	17:7893476	TCGTCGGCCACCCCC[A/C]TAGCACCCTCCGGAC	1107
rs768637813	snp	G/T			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7887464	AGATGTGATTCCTTG[G/T]GGGTGGGGGTGGGGA	1107
rs768666364	snp	C/T	0.000168226	0.00916976	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910909	CTTCAGCGCCGCACC[C/T]GTAGGGGCCCTGGCC	1107
rs768688815	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7889378	TGAAAGGACCTGCCA[C/T]AGTCAGAGCCCATGG	1107
rs768758499	snp	A/G	3.32541e-05	0.00407749	missense	CHD3	GRCh38.p7	17:7899017	TCTCTATAGCCTACC[A/G]TGAAATATGAGACTC	1107
rs768779210	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7910758	TACCCTTAGCAGTTG[C/T]GGAGTGTGGCTCATA	1107
rs768783784	snp	A/G	1.64868e-05	0.00287109	synonymous-codon	CHD3	GRCh38.p7	17:7894994	GGAAGAAGGGGAGAA[A/G]GAGGAGGAGGATGAT	1107
rs768816748	snp	A/G	1.71349e-05	0.00292697	intron-variant	CHD3	GRCh38.p7	17:7894897	TCCATCTGTCTGTGT[A/G]TCTATCCTTGGCCCC	1107
rs768818007	snp	C/G	1.71752e-05	0.00293041	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911618	CCTTCACCCAGGCCC[C/G]GTCCCCGAGGCCGAC	1107
rs768825985	in-del	-/A	0.000270038	0.0116166	intron-variant	CHD3	GRCh38.p7	17:7901037	AACGCCCATTCTCAG[-/A]AAACATGGGTGGGGA	1107
rs768832038	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7896847	TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATGT	1107
rs768894119	snp	C/T	1.70641e-05	0.00292092	intron-variant	CHD3	GRCh38.p7	17:7903803	GGAACCCAAAGTTCC[C/T]GTTTGTTTTCCCTCT	1107
rs768910172	snp	A/G	1.64817e-05	0.00287064	missense	CHD3	GRCh38.p7	17:7911496	CCAGTGCTTGTGAAG[A/G]AGGAGAAGGAAATGG	1107
rs768917093	snp	C/T	1.66718e-05	0.00288715	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904600	AGTTAACTACAATGA[C/T]GCTGCTCAGGAAGAC	1107
rs769054049	snp	C/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905336	TCTGCTAGTAAACTT[C/T]GGTGTGTGTGACCAC	1107
rs769057573	snp	C/T	3.87319e-05	0.00440051	intron-variant	CHD3	GRCh38.p7	17:7889821	CAAGGCTCAAGAGAC[C/T]CATTCTCAGAGACCT	1107
rs769080051	snp	A/C/G	6.61303e-05	0.0057499	intron-variant	CHD3	GRCh38.p7	17:7907057	GTCAGGATGGTGGGA[A/C/G]AGACAGAAAGGGAGC	1107
rs769127697	snp	C/T	1.6477e-05	0.00287024	synonymous-codon	CHD3	GRCh38.p7	17:7900350	CTGACAGGAACCCCA[C/T]TGCAGAATAATCTGG	1107
rs769244674	snp	C/T	1.66807e-05	0.00288792	intron-variant	CHD3	GRCh38.p7	17:7895572	TCTTTCCCTCTCCCC[C/T]ATGACCTCATTTCCT	1107
rs769257772	snp	A/C/T	3.31188e-05	0.00406921	missense	CHD3	GRCh38.p7	17:7910508	CTGTCCCGAATACCC[A/C/T]CCATCGCAGCCCGCC	1107
rs769353225	in-del	-/GTGTGG			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888715	TGGGCCTGAGAGTGT[-/GTGTGG]GTGTGGGTGTGGGTG	1107
rs769376343	snp	C/G	1.78306e-05	0.00298579	intron-variant	CHD3	GRCh38.p7	17:7900061	TCCAGACCTAAAAAA[C/G]TTGAAGTTGTGGACT	1107
rs769399908	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7896965	TGCCTGGGCCAATCC[A/G]TCCTTTTTCATAGCT	1107
rs769411726	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7890220	TAGATCATTTGAGGT[C/T]AGGAGTTCGCGACAA	1107
rs769436591	snp	G/T	1.64996e-05	0.0028722	missense	CHD3	GRCh38.p7	17:7906959	CGCTCCTCCAGAGCC[G/T]CCTCTCCTACCAAAA	1107
rs769460687	in-del	-/T	3.29992e-05	0.00406184	intron-variant	CHD3	GRCh38.p7	17:7907096	GGGCGGGAGAATCTC[-/T]TGTCTTTATCACTGT	1107
rs769472917	snp	A/G	1.70435e-05	0.00291915	synonymous-codon	CHD3	GRCh38.p7	17:7893328	GATCCCAATGTCTAA[A/G]ATGATGACCATCCTT	1107
rs769493703	snp	A/G	1.81724e-05	0.00301428	intron-variant	CHD3	GRCh38.p7	17:7907516	CCTTAGGAGTGATGG[A/G]GGATTAGAATTTGGG	1107
rs769511403	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7889473	CTGACCCCTGACCTC[C/T]CATTCAGAACCAGAG	1107
rs769517619	snp	A/G	0.00170213	0.0291233	synonymous-codon, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884830	CCCTCTGAGGGACGA[A/G]GAGGAGGAGGAGGAG	1107
rs769544205	snp	A/G	1.72329e-05	0.00293533	intron-variant	CHD3	GRCh38.p7	17:7897037	TCCTTGTTGTCCTCT[A/G]TGAGTGTCAGGACTA	1107
rs769544991	snp	A/G	1.64838e-05	0.00287083	synonymous-codon	CHD3	GRCh38.p7	17:7907154	AAGTGAGAAAGGAGA[A/G]GGCATAAGGACACCT	1107
rs769593528	snp	C/T	1.66488e-05	0.00288515	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906021	CAGGGCTGAGTTGGA[C/T]GCAAGGGGAAGAGCT	1107
rs769631440	snp	A/G	1.65225e-05	0.00287419	intron-variant	CHD3	GRCh38.p7	17:7907068	GGGAGAGACAGAAAG[A/G]GAGCCAGGAGTCAGG	1107
rs769668916	in-del	-/CCT	7.04635e-05	0.00593521	intron-variant	CHD3	GRCh38.p7	17:7901215	GTTTCCAACTGACCC[-/CCT]CCTCCTCCTCTCTCC	1107
rs769694017	snp	C/G	1.64879e-05	0.00287118	missense, downstream-variant-500B	CHD3	GRCh38.p7	17:7903339	GGTTTGTGACTCGCG[C/G]GTCAGTGGAAGAGCG	1107
rs769711176	snp	C/T	1.75265e-05	0.00296023	intron-variant	CHD3	GRCh38.p7	17:7894657	AGGAACCCACCCATC[C/T]CTTTCCCCCTTGGTT	1107
rs769780640	snp	A/G	3.3006e-05	0.00406226	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906602	GAGCCTGGGGCAGAC[A/G]GCTCTGAAACCTTTG	1107
rs769787126	snp	A/C	5.10009e-05	0.00504954	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906112	ACCCTCCCTGTCATA[A/C]AATACTTCCTGGCTC	1107
rs769791470	snp	A/C	1.69117e-05	0.00290785	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903232	AGCTTCTCCCCGGCC[A/C]CTCCCCTGACCCACC	1107
rs769804151	snp	A/G	1.73896e-05	0.00294865	synonymous-codon	CHD3	GRCh38.p7	17:7908451	AGCTATTTCCTCGGG[A/G]AAACTCAATGAGATC	1107
rs769887040	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7898941	TGGTATCCATGCCAG[A/G]GAGGAAGAGACTAAG	1107
rs769901709	snp	A/C	1.6525e-05	0.00287441	intron-variant	CHD3	GRCh38.p7	17:7899311	TACGGCCTCTAGCCT[A/C]GACTTATGCTGCCCC	1107
rs769902460	snp	A/C/G	4.94722e-05	0.00497333	synonymous-codon	CHD3	GRCh38.p7	17:7894467	TGATGGCTACGAGAC[A/C/G]GATCACCAGGATTAC	1107
rs769960925	snp	G/T	1.74769e-05	0.00295603	missense	CHD3	GRCh38.p7	17:7893529	TGCTGCTGATATCCA[G/T]CCCCCACCCATCCGA	1107
rs769962813	snp	A/G/T	0.000280038	0.0118298	missense	CHD3	GRCh38.p7	17:7895028	ATGGAGTACTGCCGC[A/G/T]TATGCAAGGACGGCG	1107
rs770051180	snp	C/T	1.70179e-05	0.00291696	intron-variant	CHD3	GRCh38.p7	17:7895184	CCTCTGTATTTACTG[C/T]CAGGCCTGATCCCTT	1107
rs770093135	snp	A/C	3.46711e-05	0.00416345	utr-variant-3-prime	CHD3	GRCh38.p7	17:7911710	ACTGGGCTAGGAACC[A/C]CTTTGCCCCTCTCTG	1107
rs770121903	snp	C/T	8.40937e-05	0.00648381	intron-variant	CHD3	GRCh38.p7	17:7904118	CCTCAAACAACTTCT[C/T]CGTCTAATAGGTGAG	1107
rs770138952	snp	A/C	6.88859e-05	0.00586841	intron-variant	CHD3	GRCh38.p7	17:7910624	TAGCTCCAGTTTTCC[A/C]TGTTTGTGTTCCTCC	1107
rs770157857	snp	A/G	1.75838e-05	0.00296506	intron-variant	CHD3	GRCh38.p7	17:7907870	TGTCCTGAGGTGTGA[A/G]CTTTGACCTGTCTGT	1107
rs770212064	snp	C/T	8.23798e-05	0.00641741	synonymous-codon	CHD3	GRCh38.p7	17:7903931	CACTGACGTGCAGAA[C/T]ATGAATGAGTATCTC	1107
rs770219771	snp	C/T	6.58913e-05	0.00573945	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905146	GGAGGAGGATGAAGA[C/T]TTCGATGAACGTCCT	1107
rs770273476	snp	C/G	2.48518e-05	0.00352495	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890721	CGGCGGAAAAAGGGG[C/G]AGGGAGATGGGGGGC	1107
rs770273659	snp	C/T	1.65059e-05	0.00287275	intron-variant	CHD3	GRCh38.p7	17:7899219	TGCTGGATTCTAGGA[C/T]CTTGAAGGGGACCGC	1107
rs770297193	snp	C/T	1.87795e-05	0.00306421	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906245	GCCTCTCCTGGGCTG[C/T]CCTAGCCTCACATTT	1107
rs770299523	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7891571	TAGAGTAGAAAATAG[C/T]AGAGATGGCCCAGGT	1107
rs770328640	in-del	-/GCAGCA	1.96171e-05	0.0031318	cds-indel	CHD3	GRCh38.p7	17:7893416	GTGGCGGCGGCAGCG[-/GCAGCA]GCAGCAGCAGCTGTA	1107
rs770331035	snp	C/G	1.66012e-05	0.00288103	intron-variant	CHD3	GRCh38.p7	17:7910843	TGCTTCCTCTCTGTT[C/G]CAGGCCTACCCGCCG	1107
rs770340495	snp	A/G			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905376	ATCCAGAAAGGCCAT[A/G]TCATTTTCCATTCCC	1107
rs770374165	snp	A/G	3.29995e-05	0.00406185	missense	CHD3	GRCh38.p7	17:7897279	GGATGACCGTCCACC[A/G]CATCATCAACCACAG	1107
rs770377555	snp	A/G	3.32011e-05	0.00407424	missense, intron-variant	CHD3	GRCh38.p7	17:7894118	GGCTATGGGCAGTAT[A/G]TTTTTCAGAGCGACG	1107
rs770383628	in-del	-/GAG	0.0373055	0.131381	cds-indel, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884894	GAAGAAGAGGGCGAC[-/GAG]GAGGAGGAGGAGGAG	1107
rs770465240	snp	C/T	4.11658e-05	0.00453665	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890648	CAGTGAATATGGAAC[C/T]GGACCGGGTCGGAAA	1107
rs770485352	snp	C/T	1.64841e-05	0.00287085	missense	CHD3	GRCh38.p7	17:7907165	GAGAAGGCATAAGGA[C/T]ACCTCTTGAGAAGGA	1107
rs770498658	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7903635	CTTCTTTTAGTAGCC[C/G]TTGGAGGAAGGTTGG	1107
rs770518990	snp	A/G	1.65921e-05	0.00288024	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910855	GTTCCAGGCCTACCC[A/G]CCGGGTCCCTACGCT	1107
rs770564531	snp	C/T	1.764e-05	0.00296979	intron-variant	CHD3	GRCh38.p7	17:7903779	TTCCCATCAGCCTTT[C/T]TAAACTTTGGAACCC	1107
rs770602934	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7891365	GAGCCCTCCCCTGCC[C/G]CAACAGCTCCATCTT	1107
rs770625965	snp	A/G	2.16565e-05	0.00329056	missense, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884894	GAAGAAGAGGGCGAC[A/G]AGGAGGAGGAGGAGG	1107
rs770652523	snp	C/T	1.79984e-05	0.00299981	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906202	GGGGCCAGGCATCCT[C/T]CCCAGGGGAGGGGCG	1107
rs770684156	snp	C/T	1.65831e-05	0.00287945	intron-variant	CHD3	GRCh38.p7	17:7902742	GGTGAGGGAGATACA[C/T]TGGTCCCTGGTGGGT	1107
rs770684177	snp	A/G	1.81641e-05	0.00301359	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905709	GGGCAACATTGAGGT[A/G]AGAGCTGGGCCCAGT	1107
rs770729968	snp	A/G	3.30202e-05	0.00406313	intron-variant	CHD3	GRCh38.p7	17:7907086	GCCAGGAGTCAGGGC[A/G]GGAGAATCTCTGTCT	1107
rs770744214	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7897755	TAAGGAGGGATCTCC[A/G]GGAATGTTTTGTGAT	1107
rs770770002	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905161	CTTCGATGAACGTCC[C/T]GAAGGTGGCATCTGT	1107
rs770777709	snp	A/G	1.6483e-05	0.00287076	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903361	GGAAGAGCGAATCAC[A/G]CAAGTGGCCAAGAGA	1107
rs770826179	snp	C/T	1.6476e-05	0.00287014	intron-variant	CHD3	GRCh38.p7	17:7908684	TTGATGGTTCCTTTT[C/T]CTTCATTGGTAGCCA	1107
rs770837931	snp	C/T	3.29935e-05	0.00406149	missense	CHD3	GRCh38.p7	17:7900398	CTGAACTTCCTCACC[C/T]CAGAGAGATTTAAGT	1107
rs770843387	snp	C/T	3.54799e-05	0.00421173	synonymous-codon	CHD3	GRCh38.p7	17:7893502	CGGACCCCCCGCCCT[C/T]CCACCACCCCCTGCT	1107
rs770907445	snp	C/G	5.00897e-05	0.00500423	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911604	GATCCCAGGCCTGCC[C/G]TTCACCCAGGCCCCG	1107
rs770908053	snp	C/T	0.00013157	0.00810974	synonymous-codon	CHD3	GRCh38.p7	17:7909328	GCCGGCCAACGCCGT[C/T]CTGCACAAGGGTAAG	1107
rs770909112	snp	A/G			utr-variant-3-prime	CHD3	GRCh38.p7	17:7911940	CCCAGCCGTTTCCCT[A/G]CAGAATCAGCTCTGT	1107
rs770913115	snp	A/G			utr-variant-3-prime	CHD3	GRCh38.p7	17:7911827	AGAAGTCTGGGTGGG[A/G]GATGGCTGGCAGGGT	1107
rs770934671	snp	C/T	1.75081e-05	0.00295867	intron-variant	CHD3	GRCh38.p7	17:7904121	CAAACAACTTCTTCG[C/T]CTAATAGGTGAGACT	1107
rs770947851	snp	G/T	1.73537e-05	0.0029456	intron-variant	CHD3	GRCh38.p7	17:7894870	ATCTTCCAGTTTCAT[G/T]CCTTAATTTCTTCCA	1107
rs770952876	in-del	-/GAG	0.000717617	0.0189286	cds-indel, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884935	GCCGACGAGGACGAT[-/GAG]GAGGAGGACGACGAC	1107
rs770955914	in-del	-/AGA	1.6537e-05	0.00287545	cds-indel, intron-variant	CHD3	GRCh38.p7	17:7907634	GAGAAAGGGGGGAGG[-/AGA]AGCCGTTGGATGGAC	1107
rs770972023	snp	A/G	1.65919e-05	0.00288022	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904447	TGCCCTTCAGATTGA[A/G]GAAATTGAGCGAGAG	1107
rs770977887	snp	A/T			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885976	GGCTCCACCCCCTTC[A/T]TCTCGCCGGGGCTCT	1107
rs770986938	snp	A/G	2.63224e-05	0.00362774	intron-variant	CHD3	GRCh38.p7	17:7889660	GATGCTTTTTGCTTC[A/G]AAGATAAGGATGACA	1107
rs771002766	in-del	-/TATC	1.67125e-05	0.00289067	intron-variant	CHD3	GRCh38.p7	17:7904017	TTGGGGGCCAGACAT[-/TATC]TATCCCAGGCCATCT	1107
rs771014049	snp	C/T	3.29495e-05	0.00405877	missense, intron-variant	CHD3	GRCh38.p7	17:7895396	CGGTGGGGGGAGCCA[C/T]CTGTAGCAGTGCCAG	1107
rs771025177	in-del	-/C	0.000249819	0.0111735	frameshift-variant	CHD3	GRCh38.p7	17:7893481	GCCACCCCCATAGCA[-/C]CCCTCCGGACCCCCC	1107
rs771037852	snp	A/C/G	0.000338456	0.0130046	missense	CHD3	GRCh38.p7	17:7893470	GCTGTCTCGTCGGCC[A/C/G]CCCCCATAGCACCCT	1107
rs771045107	snp	A/C			intron-variant, upstream-variant-2KB, utr-variant-5-prime	CHD3, NAA38	GRCh38.p7	17:7886964	TCAGAGGCTGCTTAC[A/C]TTTTACAACTGAAAT	1107
rs771073572	snp	C/G/T	8.55858e-05	0.00654117	missense	CHD3	GRCh38.p7	17:7907393	CACTTGGGGAGCGGC[C/G/T]GGAGCCAAGGAAGAT	1107
rs771095708	snp	C/T	3.306e-05	0.00406558	intron-variant	CHD3	GRCh38.p7	17:7893787	TTTTTCCTCTTCTCA[C/T]CCCGACTCCTCATTC	1107
rs771147785	snp	C/T	3.42436e-05	0.00413771	missense	CHD3	GRCh38.p7	17:7907381	GCCCAGCCCCATCAC[C/T]TGGGGAGCGGCTGGA	1107
rs771170143	snp	C/G	1.76201e-05	0.00296812	intron-variant	CHD3	GRCh38.p7	17:7901208	GGGGCATGTTTCCAA[C/G]TGACCCCCTCCTCCT	1107
rs771183277	snp	A/G	1.64833e-05	0.00287078	intron-variant	CHD3	GRCh38.p7	17:7889111	GCCTGGTAATTATCC[A/G]AGGAAATGTAAATAG	1107
rs771185332	snp	A/G	1.6477e-05	0.00287024	missense	CHD3	GRCh38.p7	17:7893840	AGTAAGAGCCCCCGA[A/G]TGCCTGATGGACGCA	1107
rs771228966	snp	G/T	3.30797e-05	0.00406679	intron-variant	CHD3	GRCh38.p7	17:7899233	ACCTTGAAGGGGACC[G/T]CCTGGACTGGGGAAG	1107
rs771229411	snp	A/C	1.67877e-05	0.00289716	intron-variant	CHD3	GRCh38.p7	17:7910346	CCTGTATCTGTCCAT[A/C]TGATGCCTCTCTTTT	1107
rs771255294	snp	G/T			missense	CHD3	GRCh38.p7	17:7902682	GAGCGCATCGATGGT[G/T]GTATCACGGGTGCCC	1107
rs771264568	snp	A/G	3.33483e-05	0.00408327	intron-variant	CHD3	GRCh38.p7	17:7898140	TCAAGGGATTCTGAC[A/G]ATGAGGGCATGAAAG	1107
rs771266385	in-del	-/GAA	2.09567e-05	0.00323696	cds-indel	CHD3	GRCh38.p7	17:7890665	GACCGGGTCGGAAAC[-/GAA]GAAGGAAGCACCGAG	1107
rs771287937	snp	A/G	2.42462e-05	0.00348174	intron-variant	CHD3	GRCh38.p7	17:7890754	AAGGTGAGTAGAATT[A/G]GGGAATGAGAGTGAG	1107
rs771305293	snp	A/G			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883726	TTGTGACTTCAATGA[A/G]GTATGTAGAAACAGA	1107
rs771333739	snp	C/T	8.56759e-05	0.00654451	intron-variant	CHD3	GRCh38.p7	17:7895201	AGGCCTGATCCCTTC[C/T]CCCATCCCTGGGGCC	1107
rs771395081	snp	A/T			intron-variant	CHD3	GRCh38.p7	17:7908958	GGGCCAAGACCAAAG[A/T]GTAACCTTGTGCTTG	1107
rs771471959	in-del	-/CCGTAGGGGCCCTGGCCG	1.68279e-05	0.00290064	cds-indel	CHD3	GRCh38.p7	17:7910907	CCTTCAGCGCCGCAC[-/CCGTAGGGGCCCTGGCCG]CCGTAGGGGCCCTGG	1107
rs771507138	snp	A/G	3.29603e-05	0.00405944	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890942	CCCTCTCCCGCAGCA[A/G]GTGGAACAGAAGTCA	1107
rs771529896	snp	C/T	1.6549e-05	0.0028765	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906632	GCCGATGGGGTCCCT[C/T]GGGAGGGACTGAGTC	1107
rs771565667	snp	A/T	1.64765e-05	0.00287019	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890958	GTGGAACAGAAGTCA[A/T]CAGCAACTCTGCTTC	1107
rs771586439	snp	C/T	3.39599e-05	0.00412053	synonymous-codon	CHD3	GRCh38.p7	17:7908015	CGCCGATGGTGGCTT[C/T]ACAGGTTGGGGAGAC	1107
rs771611554	snp	A/G	1.65943e-05	0.00288043	missense, synonymous-codon	CHD3	GRCh38.p7	17:7910860	AGGCCTACCCGCCGG[A/G]TCCCTACGCTACACC	1107
rs771632248	snp	C/T	1.70842e-05	0.00292264	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905734	CCCAGTGTTCCTGAG[C/T]TCTCCAAGAGGGCAT	1107
rs771656412	in-del	-/CCT	1.65499e-05	0.00287657	cds-indel	CHD3	GRCh38.p7	17:7907929	GAGCTTCGACCAGGG[-/CCT]CGAGATGAGCCACGG	1107
rs771669987	snp	C/T	0.000149003	0.00863014	missense	CHD3	GRCh38.p7	17:7894241	AAACTAAAGAGAGGC[C/T]GGCCAGGAAGGAAGA	1107
rs771700787	snp	A/G	1.64822e-05	0.00287068	missense	CHD3	GRCh38.p7	17:7900703	AAGACAGAGCTCATC[A/G]TTCGGGTGGAGCTAA	1107
rs771732380	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7892693	GTAGAGACGGGGTTT[C/T]GCCATGTTGGCCAGG	1107
rs771757800	snp	A/G	3.4167e-05	0.00413308	intron-variant	CHD3	GRCh38.p7	17:7894313	GTGGGCCGTCCTCTC[A/G]TTCTTATTTTCAATT	1107
rs771830862	snp	G/T	1.67385e-05	0.00289292	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903105	ACCATTTAGCAAGGA[G/T]ATGTGGGTTCATGGA	1107
rs771832962	snp	C/T	1.64898e-05	0.00287135	missense	CHD3	GRCh38.p7	17:7899374	CCTTCCTGGTGAGTG[C/T]CCCACTCTCTACCAT	1107
rs771860156	snp	C/T	1.79242e-05	0.00299362	intron-variant	CHD3	GRCh38.p7	17:7909121	AGAGCCCTACCTTCA[C/T]CTCCCAACTCTGTGC	1107
rs771872726	snp	C/G/T	4.94338e-05	0.00497141	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905187	TCTGTGTTCCTGACT[C/G/T]TACCTCACCTCTTCC	1107
rs771926481	snp	C/T	1.65258e-05	0.00287448	intron-variant	CHD3	GRCh38.p7	17:7900438	CCTAAGGGTAGTTGG[C/T]AGAGATGAGAGGTGG	1107
rs771976061	snp	A/G	1.64741e-05	0.00286998	intron-variant, synonymous-codon	CHD3	GRCh38.p7	17:7889078	TTTTCCTCCAGGACT[A/G]TGTTGGGGTGACAGG	1107
rs771984924	snp	C/G/T	3.36855e-05	0.00410388	missense	CHD3	GRCh38.p7	17:7898579	GTGATGGGCCTCCCA[C/G/T]TTCTCCCACTAATGA	1107
rs771986812	snp	C/T	3.31153e-05	0.00406898	intron-variant	CHD3	GRCh38.p7	17:7897304	CCACAGGTGAATCCT[C/T]GGTCCCTGGGAAGTC	1107
rs771996106	snp	A/C	0.000621034	0.0176105	synonymous-codon	CHD3	GRCh38.p7	17:7893508	CCCCGCCCTTCCACC[A/C]CCCCCTGCTGCTGAT	1107
rs772016628	snp	A/G	1.64762e-05	0.00287016	synonymous-codon	CHD3	GRCh38.p7	17:7903913	CCAGGATGCAACTGA[A/G]GACACTGACGTGCAG	1107
rs772056098	snp	G/T	1.75111e-05	0.00295893	synonymous-codon	CHD3	GRCh38.p7	17:7909304	CAAGGAGTCGCTGGC[G/T]GGGAACAAGCCGGCC	1107
rs772073065	snp	C/T	1.74391e-05	0.00295283	intron-variant	CHD3	GRCh38.p7	17:7901222	ACTGACCCCCTCCTC[C/T]TCCTCTCTCCTCCCT	1107
rs772100845	snp	C/T	4.94474e-05	0.00497205	synonymous-codon	CHD3	GRCh38.p7	17:7900702	CAAGACAGAGCTCAT[C/T]GTTCGGGTGGAGCTA	1107
rs772114836	snp	A/G			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886125	TCGCTGAAACCACCC[A/G]CTCCCTGAGCACGTT	1107
rs772132381	snp	G/T	1.69037e-05	0.00290716	intron-variant	CHD3	GRCh38.p7	17:7893959	CCCGTCCCTGTCTAC[G/T]AAACACCTGGGGGCC	1107
rs772172343	snp	A/C	4.94262e-05	0.00497098	intron-variant, missense	CHD3	GRCh38.p7	17:7889005	TCTCCTGTGTGATGA[A/C]GGCGGCAGACACTGT	1107
rs772190878	in-del	-/A	1.67902e-05	0.00289738	intron-variant	CHD3	GRCh38.p7	17:7895163	ACAGTGAGTGGAAAC[-/A]TCTCCCCTCTGTATT	1107
rs772209811	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7895284	ATCTTCTCATCTAAC[A/G]ATGGGTTCTTTCTGC	1107
rs772231915	snp	A/G	5.95622e-05	0.00545688	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889689	CATTCGGCTGCTGCC[A/G]TCAGCATTGGGTGTG	1107
rs772247614	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7911349	TCTTCCCTCCCTCAC[G/T]TGGGACAACGGGAAG	1107
rs772286724	snp	A/T	1.6477e-05	0.00287024	synonymous-codon	CHD3	GRCh38.p7	17:7894512	GCAGGGTGGGGAAAT[A/T]ATTCTGTGTGACACC	1107
rs772304301	snp	A/G	1.70345e-05	0.00291838	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906116	TCCCTGTCATACAAT[A/G]CTTCCTGGCTCGATT	1107
rs772319972	snp	C/G/T	6.74065e-05	0.00580513	intron-variant	CHD3	GRCh38.p7	17:7889810	TAACTCTGTGGCAAG[C/G/T]CTCAAGAGACCCATT	1107
rs772329005	snp	C/G	1.67175e-05	0.0028911	intron-variant	CHD3	GRCh38.p7	17:7899005	TCTGACTTCTTGTCT[C/G]TATAGCCTACCGTGA	1107
rs772422254	snp	G/T	1.66974e-05	0.00288936	intron-variant	CHD3	GRCh38.p7	17:7895297	ACAATGGGTTCTTTC[G/T]GCCTCTTTCTTTCCT	1107
rs772437953	snp	A/G	3.31378e-05	0.00407036	intron-variant	CHD3	GRCh38.p7	17:7906828	TTCCTGTCTGTAAGC[A/G]CCTGGAGCTGACACC	1107
rs772539844	snp	G/T	1.67677e-05	0.00289544	intron-variant	CHD3	GRCh38.p7	17:7894080	AGGGCGTAGAATGAA[G/T]TCTGCCTCACTGACG	1107
rs772543789	snp	A/G	1.64762e-05	0.00287016	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904524	TGCTGAGGCATCACT[A/G]TGAGCAACAGCAGGA	1107
rs772599946	snp	G/T	1.68846e-05	0.00290552	intron-variant	CHD3	GRCh38.p7	17:7899569	CTACCTCATATCCTC[G/T]GAGACCCTCAAAGCT	1107
rs772633618	snp	A/G	0.000130014	0.00806163	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904129	TTCTTCGTCTAATAG[A/G]TGAGACTGGACTTCA	1107
rs772660598	snp	C/T	3.29739e-05	0.00406028	intron-variant	CHD3	GRCh38.p7	17:7908677	AAATTCCTTGATGGT[C/T]CCTTTTCCTTCATTG	1107
rs772690169	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant	CHD3	GRCh38.p7	17:7895408	CCACCTGTAGCAGTG[C/T]CAGCCCCTCAACAGG	1107
rs772711535	snp	A/G	0.0109686	0.0732392	synonymous-codon, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884848	GGAGGAGGAGGAGGA[A/G]ATGGTGGTGTCGGAG	1107
rs772811110	snp	A/T	1.65957e-05	0.00288055	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7894120	CTATGGGCAGTATGT[A/T]TTTCAGAGCGACGAA	1107
rs772830602	snp	A/G	1.65143e-05	0.00287348	intron-variant	CHD3	GRCh38.p7	17:7907082	GGGAGCCAGGAGTCA[A/G]GGCGGGAGAATCTCT	1107
rs772856184	snp	A/G	1.65803e-05	0.00287922	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910528	CGCAGCCCGCCTTCA[A/G]ATGTCCGAGCGCAGC	1107
rs772865958	snp	C/T	1.79155e-05	0.0029929	intron-variant	CHD3	GRCh38.p7	17:7901419	TCTGCTTCCTCTTCC[C/T]TCTCCTCATCCTCCA	1107
rs772883875	snp	C/T	7.02568e-05	0.0059265	intron-variant	CHD3	GRCh38.p7	17:7890538	TGGCAATGGTAGGGA[C/T]GAATAAATGTTATTT	1107
rs772927430	snp	C/G	1.6501e-05	0.00287232	missense	CHD3	GRCh38.p7	17:7906963	CCTCCAGAGCCTCCT[C/G]TCCTACCAAAACGTC	1107
rs772956656	snp	A/G			utr-variant-3-prime	CHD3	GRCh38.p7	17:7911783	CCACACACCTTTCCC[A/G]CCAAGCCTTGAAGAC	1107
rs772975970	snp	C/T	1.69341e-05	0.00290977	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903234	CTTCTCCCCGGCCAC[C/T]CCCCTGACCCACCCG	1107
rs772997871	snp	C/T	1.6981e-05	0.00291379	synonymous-codon	CHD3	GRCh38.p7	17:7893337	GTCTAAGATGATGAC[C/T]ATCCTTGGGGCCAAA	1107
rs773009765	snp	C/T	4.94246e-05	0.0049709	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7891028	AGGAGGATTACCACA[C/T]GCTCACCAACTACAA	1107
rs773015821	in-del	-/AGAT	1.65559e-05	0.00287709	intron-variant	CHD3	GRCh38.p7	17:7902734	GTTTAATGGTGAGGG[-/AGAT]AGATACACTGGTCCC	1107
rs773042804	snp	A/G	1.70078e-05	0.0029161	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906113	CCCTCCCTGTCATAC[A/G]ATACTTCCTGGCTCG	1107
rs773079818	snp	A/G	1.65581e-05	0.00287728	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906633	CCGATGGGGTCCCTC[A/G]GGAGGGACTGAGTCG	1107
rs773081698	snp	A/C/G	9.99417e-05	0.0070683	missense	CHD3	GRCh38.p7	17:7910886	ACACCTCCGGGGTAC[A/C/G]GGGCGGCCTTCAGCG	1107
rs773082340	snp	C/T	0.000178314	0.0094406	intron-variant	CHD3	GRCh38.p7	17:7900062	CCAGACCTAAAAAAC[C/T]TGAAGTTGTGGACTT	1107
rs773124354	snp	C/G	3.95155e-05	0.0044448	utr-variant-3-prime	CHD3	GRCh38.p7	17:7911745	TCCTCTCTTCAAGAA[C/G]GGCCCTTTGTCTTTC	1107
rs773154603	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7897671	TGTATTTAGTTATTT[C/G]AATGCTGCCTTCCCC	1107
rs773170300	snp	A/G	0.000164864	0.00907771	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903340	GTTTGTGACTCGCGC[A/G]TCAGTGGAAGAGCGA	1107
rs773170877	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7908282	CTAACCTTTACCCAT[C/T]CCTCTTCAGGAGCCC	1107
rs773173063	snp	C/T			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883133	CTTTGGGACTCCTTT[C/T]CAACTGTCCAATTCC	1107
rs773185315	in-del	-/TGG			cds-indel	CHD3	GRCh38.p7	17:7911509	AGAAGGAGAAGGAAA[-/TGG]TGGGGGCATTGGTGT	1107
rs773191512	snp	A/T	1.64762e-05	0.00287016	intron-variant, missense	CHD3	GRCh38.p7	17:7889095	GTTGGGGTGACAGGA[A/T]GCCTGGTAATTATCC	1107
rs773209157	snp	C/T	1.65943e-05	0.00288043	intron-variant	CHD3	GRCh38.p7	17:7893772	TGTCATGACCTCTCC[C/T]TTTTCCTCTTCTCAC	1107
rs773212331	snp	A/C	6.94517e-05	0.00589245	missense	CHD3	GRCh38.p7	17:7908452	GCTATTTCCTCGGGG[A/C]AACTCAATGAGATCT	1107
rs773249352	in-del	-/AAG	0.00346088	0.0414544	cds-indel	CHD3	GRCh38.p7	17:7898538	CAGCCCCGCAAGTAT[-/AAG]AAGAAGAAGAAGAAG	1107
rs773259292	snp	C/T	1.66529e-05	0.00288551	intron-variant	CHD3	GRCh38.p7	17:7897332	GTCAGACCTGGTATA[C/T]GACATTATTCTTACC	1107
rs773279100	snp	C/G	1.64746e-05	0.00287002	intron-variant, missense	CHD3	GRCh38.p7	17:7889019	AAGGCGGCAGACACT[C/G]TGATCCTGTGGGCAA	1107
rs773301679	snp	C/T	0.000126719	0.00795885	missense	CHD3	GRCh38.p7	17:7909179	ATTGAGGAGCAGCTG[C/T]GGCGGGCGGCCTACC	1107
rs773318666	snp	C/T	0.000130847	0.00808743	synonymous-codon	CHD3	GRCh38.p7	17:7909322	GAACAAGCCGGCCAA[C/T]GCCGTCCTGCACAAG	1107
rs773388851	snp	A/G	1.7736e-05	0.00297787	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911625	CCAGGCCCCGTCCCC[A/G]AGGCCGACCCCCAGC	1107
rs773411857	snp	C/T	1.75471e-05	0.00296197	missense	CHD3	GRCh38.p7	17:7893534	CTGATATCCAGCCCC[C/T]ACCCATCCGAAGAGC	1107
rs773416384	snp	A/G	1.64765e-05	0.00287019	missense	CHD3	GRCh38.p7	17:7903932	ACTGACGTGCAGAAC[A/G]TGAATGAGTATCTCA	1107
rs773443328	snp	A/C	1.6525e-05	0.00287441	synonymous-codon	CHD3	GRCh38.p7	17:7902718	CAGGAGGCCATCGAT[A/C]GGTTTAATGGTGAGG	1107
rs773516185	snp	G/T	1.70226e-05	0.00291736	intron-variant	CHD3	GRCh38.p7	17:7894905	TCTGTGTGTCTATCC[G/T]TGGCCCCCTAGGAGA	1107
rs773617370	snp	C/T	1.8866e-05	0.00307126	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906248	TCTCCTGGGCTGTCC[C/T]AGCCTCACATTTACT	1107
rs773624211	snp	A/G	3.45513e-05	0.00415625	intron-variant	CHD3	GRCh38.p7	17:7910630	CAGTTTTCCCTGTTT[A/G]TGTTCCTCCTGCACA	1107
rs773690122	snp	A/G	1.71702e-05	0.00292998	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905731	GGGCCCAGTGTTCCT[A/G]AGTTCTCCAAGAGGG	1107
rs773705442	snp	A/G	1.65241e-05	0.00287433	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906620	TCTGAAACCTTTGCC[A/G]ATGGGGTCCCTCGGG	1107
rs773741525	snp	A/G	3.30131e-05	0.00406269	missense	CHD3	GRCh38.p7	17:7907234	GCAGAATTGGGGAGA[A/G]GATGGAGACAGAGGT	1107
rs773789216	snp	C/T	1.75554e-05	0.00296267	intron-variant	CHD3	GRCh38.p7	17:7907871	GTCCTGAGGTGTGAG[C/T]TTTGACCTGTCTGTC	1107
rs773794684	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7893031	AAGCAATCCTCCTGC[C/T]TCAGCCTGGAATTAC	1107
rs773838784	snp	G/T			missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889669	TGCTTCAAAGATAAG[G/T]ATGACATTCGGCTGC	1107
rs773876107	in-del	-/GAG	0.0373055	0.131381	cds-indel, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884893	GAAGAAGAGGGCGAC[-/GAG]GAGGAGGAGGAGGAG	1107
rs773935537	in-del	-/CTT	1.71634e-05	0.0029294	intron-variant	CHD3	GRCh38.p7	17:7904113	GTGGACCTCAAACAA[-/CTT]CTTCGTCTAATAGGT	1107
rs774001960	snp	C/T	5.53541e-05	0.00526061	missense, intron-variant	CHD3	GRCh38.p7	17:7907670	AACACAGGGAGAGGC[C/T]GGAGGGGGAAACAGG	1107
rs774005018	snp	A/G	1.65378e-05	0.00287552	intron-variant	CHD3	GRCh38.p7	17:7899237	TGAAGGGGACCGCCT[A/G]GACTGGGGAAGTGGG	1107
rs774087352	snp	C/T	1.64844e-05	0.00287087	missense	CHD3	GRCh38.p7	17:7907167	GAAGGCATAAGGACA[C/T]CTCTTGAGAAGGAGG	1107
rs774094485	snp	C/T	1.64811e-05	0.00287059	stop-gained, downstream-variant-500B	CHD3	GRCh38.p7	17:7902975	TTCCTCCTGTCCACC[C/T]GAGCTGGGGGCCTGG	1107
rs774181318	snp	C/T	0.000702988	0.018735	intron-variant	CHD3	GRCh38.p7	17:7909096	CCCCAGCCCCTCACC[C/T]ACTGCTGGCAGAGCC	1107
rs774186605	snp	C/T	3.31598e-05	0.00407171	intron-variant	CHD3	GRCh38.p7	17:7902743	GTGAGGGAGATACAC[C/T]GGTCCCTGGTGGGTG	1107
rs774192352	snp	C/G	1.64819e-05	0.00287066	missense	CHD3	GRCh38.p7	17:7911487	AACGGCCCTCCAGTG[C/G]TTGTGAAGAAGGAGA	1107
rs774221249	snp	A/G	0.00226443	0.0335721	synonymous-codon, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884902	GGGCGACGAGGAGGA[A/G]GAGGAGGAGGTGGAG	1107
rs774228810	snp	A/G	0.000181206	0.00951683	missense	CHD3	GRCh38.p7	17:7897186	AGGATGATGGGAAGA[A/G]CGACAAGCGTAAAGT	1107
rs774242506	in-del	-/TCCGGA	0.000121716	0.00780021	cds-indel	CHD3	GRCh38.p7	17:7893485	ACCCCCATAGCACCC[-/TCCGGA]CCCCCCGCCCTTCCA	1107
rs774249468	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7906784	TGAGTTGTAAGCTTG[C/T]GCTGGTGTGAGACGG	1107
rs774266856	snp	C/T			utr-variant-3-prime	CHD3	GRCh38.p7	17:7912002	GGCCTTTAGGAACTT[C/T]TGTGGGGAAGAGAGC	1107
rs774290809	snp	C/G			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883019	AACAAGAATGAAAGA[C/G]GGTAGAACTGAGCTA	1107
rs774312586	snp	C/T			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888396	TCCTAGAGCTAGGGG[C/T]TGGGCCAAGCCCAGG	1107
rs774318825	snp	A/G	1.70945e-05	0.00292351	intron-variant	CHD3	GRCh38.p7	17:7897048	CTCTGTGAGTGTCAG[A/G]ACTATCTCTTTCCCT	1107
rs774318924	snp	C/T	1.65132e-05	0.00287339	intron-variant	CHD3	GRCh38.p7	17:7900424	TAAGTAAGTGGTTCC[C/T]TAAGGGTAGTTGGCA	1107
rs774364338	snp	A/G	1.65021e-05	0.00287241	intron-variant	CHD3	GRCh38.p7	17:7907092	AGTCAGGGCGGGAGA[A/G]TCTCTGTCTTTATCA	1107
rs774377189	snp	C/T	1.65315e-05	0.00287498	intron-variant	CHD3	GRCh38.p7	17:7899231	GGACCTTGAAGGGGA[C/T]CGCCTGGACTGGGGA	1107
rs774456857	in-del	-/A	1.78487e-05	0.00298731	intron-variant	CHD3	GRCh38.p7	17:7907862	GAGGAGGGTGTCCTG[-/A]GGTGTGAGCTTTGAC	1107
rs774463931	snp	C/T	1.71622e-05	0.0029293	missense	CHD3	GRCh38.p7	17:7907389	CCATCACTTGGGGAG[C/T]GGCTGGAGCCAAGGA	1107
rs774485029	snp	A/G	1.64963e-05	0.00287192	synonymous-codon	CHD3	GRCh38.p7	17:7900969	GTGCTGCAACCATCC[A/G]TACCTTTTTCCCGTG	1107
rs774535052	snp	G/T	1.64852e-05	0.00287094	intron-variant	CHD3	GRCh38.p7	17:7889113	CTGGTAATTATCCGA[G/T]GAAATGTAAATAGAG	1107
rs774537067	snp	A/G	1.6476e-05	0.00287014	synonymous-codon	CHD3	GRCh38.p7	17:7893851	CCGAGTGCCTGATGG[A/G]CGCAAGAAGCTTCGG	1107
rs774614302	snp	C/T	3.42783e-05	0.0041398	intron-variant	CHD3	GRCh38.p7	17:7894394	CCTGCTTCCTTATCC[C/T]TCCACCGGGGTATAT	1107
rs774619622	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7895204	CCTGATCCCTTCCCC[C/T]ATCCCTGGGGCCCAC	1107
rs774623583	in-del	-/C	6.68606e-05	0.00578151	frameshift-variant, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7885003	CCGCGACCGCCACAG[-/C]CCCCCCCGGCTGCCA	1107
rs774624950	snp	A/G	2.24374e-05	0.00334936	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889672	TTCAAAGATAAGGAT[A/G]ACATTCGGCTGCTGC	1107
rs774628550	snp	A/G	0.000190096	0.0097474	intron-variant, missense	CHD3	GRCh38.p7	17:7909344	CTGCACAAGGGTAAG[A/G]GCCGCGGCGGCCCCG	1107
rs774733248	snp	A/C	1.65269e-05	0.00287457	intron-variant	CHD3	GRCh38.p7	17:7893788	TTTTCCTCTTCTCAC[A/C]CCGACTCCTCATTCA	1107
rs774748581	snp	C/T	3.2993e-05	0.00406145	synonymous-codon	CHD3	GRCh38.p7	17:7903970	CAAGGTGGCACAGTA[C/T]GTCGTGCGGGAAGAA	1107
rs774761554	snp	A/G	1.67108e-05	0.00289052	intron-variant	CHD3	GRCh38.p7	17:7898145	GGATTCTGACGATGA[A/G]GGCATGAAAGCCAAA	1107
rs774851044	snp	C/T	1.64811e-05	0.00287059	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7902986	CACCCGAGCTGGGGG[C/T]CTGGGCATCAATCTG	1107
rs774860426	snp	C/T	0.000317276	0.0125912	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904123	AACAACTTCTTCGTC[C/T]AATAGGTGAGACTGG	1107
rs774890132	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7894711	AGATGGCTGGACTTC[G/T]TAGTAACAGATGTCC	1107
rs774913196	snp	A/G	1.64754e-05	0.00287009	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890964	CAGAAGTCATCAGCA[A/G]CTCTGCTTCTGACCT	1107
rs774919960	snp	A/G	1.64746e-05	0.00287002	missense	CHD3	GRCh38.p7	17:7895040	CGCGTATGCAAGGAC[A/G]GCGGGGAGCTCCTGT	1107
rs774924497	snp	C/T	3.31983e-05	0.00407407	missense	CHD3	GRCh38.p7	17:7910865	TACCCGCCGGGTCCC[C/T]ACGCTACACCTCCGG	1107
rs774958880	in-del	-/TCT	1.74758e-05	0.00295594	intron-variant	CHD3	GRCh38.p7	17:7908058	TGCTCCTCAAGGGGA[-/TCT]TCTGCTCATCCTCAT	1107
rs775007526	in-del	-/TCAGCTGGTGTTT	3.38966e-05	0.00411669	splice-donor-variant	CHD3	GRCh38.p7	17:7910975	GTCCTTCATCACAGG[-/TCAGCTGGTGTTT]TCCTACCCCCTGCTA	1107
rs775054365	snp	A/G	1.65608e-05	0.00287752	intron-variant	CHD3	GRCh38.p7	17:7906833	GTCTGTAAGCGCCTG[A/G]AGCTGACACCTAACC	1107
rs775091618	snp	C/T			utr-variant-3-prime, downstream-variant-500B	CHD3	GRCh38.p7	17:7912208	CTGGCTCAGTTACCT[C/T]CTGTGTACCGGCATC	1107
rs775108956	snp	C/T	8.37907e-05	0.00647212	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910903	GGCGGCCTTCAGCGC[C/T]GCACCCGTAGGGGCC	1107
rs775142325	snp	G/T	1.66283e-05	0.00288338	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906648	GGGAGGGACTGAGTC[G/T]CCAGCAGGTGTTGAC	1107
rs775184688	snp	A/G	3.34001e-05	0.00408643	intron-variant	CHD3	GRCh38.p7	17:7895298	CAATGGGTTCTTTCT[A/G]CCTCTTTCTTTCCTC	1107
rs775225065	snp	C/T	3.29755e-05	0.00406038	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905805	GTAGAAAGGACAAGA[C/T]CTAAGAACCCTAGAC	1107
rs775232395	snp	A/C	3.42924e-05	0.00414065	intron-variant	CHD3	GRCh38.p7	17:7908029	TCACAGGTTGGGGAG[A/C]CTCTCGCTGCTTTCT	1107
rs775242396	snp	A/G	4.94621e-05	0.00497279	missense	CHD3	GRCh38.p7	17:7907179	ACACCTCTTGAGAAG[A/G]AGGAAGCTGAAAACC	1107
rs775301861	snp	A/G	1.65622e-05	0.00287764	missense	CHD3	GRCh38.p7	17:7894242	AACTAAAGAGAGGCC[A/G]GCCAGGAAGGAAGAA	1107
rs775326102	snp	A/C	1.64893e-05	0.0028713	synonymous-codon	CHD3	GRCh38.p7	17:7899375	CTTCCTGGTGAGTGC[A/C]CCACTCTCTACCATC	1107
rs775330731	snp	C/T	0.000115774	0.00760748	intron-variant	CHD3	GRCh38.p7	17:7909134	CACCTCCCAACTCTG[C/T]GCCCTCAGCTCCTGG	1107
rs775437092	snp	A/G	3.30879e-05	0.00406729	intron-variant	CHD3	GRCh38.p7	17:7907279	ATTCCCCTGTGGAGC[A/G]GGAGGGGAGGGGGCT	1107
rs775437340	snp	G/T	1.67217e-05	0.00289147	intron-variant	CHD3	GRCh38.p7	17:7902779	GGCCTGAGAAACCTG[G/T]GATAGGTCCCTGGGA	1107
rs775454595	snp	C/T	1.65233e-05	0.00287426	intron-variant	CHD3	GRCh38.p7	17:7900804	AGTGCAATATCATAA[C/T]TGCTTCCTTTATTTA	1107
rs775454952	snp	A/C			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886185	CTGCAGCTTGACCAT[A/C]ACTCAGCACCCGTCC	1107
rs775468708	snp	C/T	1.73682e-05	0.00294683	intron-variant	CHD3	GRCh38.p7	17:7894871	TCTTCCAGTTTCATT[C/T]CTTAATTTCTTCCAT	1107
rs775508156	snp	A/C			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7887091	TCGGAGGTAAAACTT[A/C]GGGAAATTATTTTTA	1107
rs775517469	snp	A/G	1.64955e-05	0.00287184	missense, downstream-variant-500B	CHD3	GRCh38.p7	17:7903405	CACACCTGGTTGTGC[A/G]GCCTGGGCTGGGCTC	1107
rs775581978	snp	C/T			missense, downstream-variant-500B	CHD3	GRCh38.p7	17:7903404	ACACACCTGGTTGTG[C/T]GGCCTGGGCTGGGCT	1107
rs775605435	snp	C/T	1.70664e-05	0.00292112	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906117	CCCTGTCATACAATA[C/T]TTCCTGGCTCGATTT	1107
rs775628098	snp	C/T	3.33806e-05	0.00408524	intron-variant	CHD3	GRCh38.p7	17:7899008	GACTTCTTGTCTCTA[C/T]AGCCTACCGTGAAAT	1107
rs775654737	snp	A/G	1.64749e-05	0.00287005	missense	CHD3	GRCh38.p7	17:7893855	GTGCCTGATGGACGC[A/G]AGAAGCTTCGGGGAA	1107
rs775657174	snp	C/G	3.29538e-05	0.00405904	synonymous-codon	CHD3	GRCh38.p7	17:7894527	TATTCTGTGTGACAC[C/G]TGCCCTCGTGCCTAC	1107
rs775659956	in-del	-/CTGT	1.69421e-05	0.00291046	intron-variant	CHD3	GRCh38.p7	17:7895181	TCCCCTCTGTATTTA[-/CTGT]CAGGCCTGATCCCTT	1107
rs775691801	snp	C/T	1.85269e-05	0.00304354	intron-variant	CHD3	GRCh38.p7	17:7907540	ATTTGGGATTTCCCT[C/T]TTCTGGGGTCAGGGG	1107
rs775714799	in-del	-/ATCCAGAGACAGGGATCCGTGAGGGCCAAGA	3.34739e-05	0.00409095	intron-variant	CHD3	GRCh38.p7	17:7893978	ACCTGGGGGCCAAGG[lengthTooLong]ATCCAGAGACAGGGA	1107
rs775748493	snp	C/T	0.00011585	0.00760997	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889696	CTGCTGCCGTCAGCA[C/T]TGGGTGTGAAGAAGA	1107
rs775779961	snp	C/G	3.30994e-05	0.004068	missense	CHD3	GRCh38.p7	17:7910505	ACGCTGTCCCGAATA[C/G]CCCCCATCGCAGCCC	1107
rs775923538	snp	C/T	1.73387e-05	0.00294432	intron-variant	CHD3	GRCh38.p7	17:7901231	CTCCTCCTCCTCTCT[C/T]CTCCCTTTTCAGGAG	1107
rs776002121	snp	A/G	1.69778e-05	0.00291352	intron-variant	CHD3	GRCh38.p7	17:7899580	CCTCTGAGACCCTCA[A/G]AGCTGTCACTTCTTT	1107
rs776015290	snp	C/T	1.6612e-05	0.00288196	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904594	CAAGCAAGTTAACTA[C/T]AATGATGCTGCTCAG	1107
rs776057008	snp	A/G	4.95544e-05	0.00497742	intron-variant	CHD3	GRCh38.p7	17:7893791	TCCTCTTCTCACCCC[A/G]ACTCCTCATTCAGGT	1107
rs776126852	snp	A/G	2.00014e-05	0.00316233	intron-variant	CHD3	GRCh38.p7	17:7893282	TCTGCTTCTATATTT[A/G]CAGGCCCCTAATTGC	1107
rs776133427	snp	C/G	3.29462e-05	0.00405857	missense, intron-variant	CHD3	GRCh38.p7	17:7895414	GTAGCAGTGCCAGCC[C/G]CTCAACAGGCAGATG	1107
rs776230186	snp	C/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895443	TGGAAATCCAGATGT[C/G]CCACCCCCCCGTCCT	1107
rs776230545	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7896922	CCTGAGCCTCCTAAA[G/T]CACTGGGATTACAGG	1107
rs776250229	snp	A/G	3.53607e-05	0.00420465	missense	CHD3	GRCh38.p7	17:7908440	GAGGAACGGGCAGCT[A/G]TTTCCTCGGGGAAAC	1107
rs776281485	snp	C/T	1.67548e-05	0.00289432	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904605	ACTACAATGATGCTG[C/T]TCAGGAAGACCAAGG	1107
rs776320089	snp	A/G	1.66746e-05	0.00288739	intron-variant	CHD3	GRCh38.p7	17:7895573	CTTTCCCTCTCCCCC[A/G]TGACCTCATTTCCTG	1107
rs776338432	snp	A/G	1.7265e-05	0.00293806	intron-variant	CHD3	GRCh38.p7	17:7908035	GTTGGGGAGACTCTC[A/G]CTGCTTTCTGCTCCT	1107
rs776341186	in-del	-/C	1.67725e-05	0.00289585	intron-variant	CHD3	GRCh38.p7	17:7895585	CCCATGACCTCATTT[-/C]CTGCCATCCTCTCCC	1107
rs776370829	snp	A/G	3.29897e-05	0.00406125	missense	CHD3	GRCh38.p7	17:7906945	GCGCCGATTCTAAGC[A/G]CTCCTCCAGAGCCTC	1107
rs776428725	snp	G/T	1.66313e-05	0.00288364	missense	CHD3	GRCh38.p7	17:7894255	CCGGCCAGGAAGGAA[G/T]AAGAAGAAGGGTAAG	1107
rs776429905	snp	C/T	1.71823e-05	0.00293101	intron-variant	CHD3	GRCh38.p7	17:7894384	CTCCCCCTGCCCTGC[C/T]TCCTTATCCCTCCAC	1107
rs776478736	snp	A/G	1.65449e-05	0.00287614	intron-variant	CHD3	GRCh38.p7	17:7907284	CCTGTGGAGCGGGAG[A/G]GGAGGGGGCTTGGAG	1107
rs776546162	in-del	-/GAGACAGGGATCCGTGAGGGCCAAGGATCCG	1.67242e-05	0.00289168	intron-variant	CHD3	GRCh38.p7	17:7893983	GGGGCCAAGGATCCA[lengthTooLong]GAGACAGGGATCCGT	1107
rs776577787	snp	A/G	1.64827e-05	0.00287073	missense	CHD3	GRCh38.p7	17:7899417	GCGGGAGTTCCAGAT[A/G]TGGGCACCCAAATTC	1107
rs776603926	snp	A/C	1.73429e-05	0.00294468	missense	CHD3	GRCh38.p7	17:7893509	CCCGCCCTTCCACCA[A/C]CCCCTGCTGCTGATA	1107
rs776611931	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7909672	ATCATCCAGTTAGGG[C/G]CCTTGGACTGTGAAT	1107
rs776663079	snp	A/T	1.65277e-05	0.00287464	intron-variant	CHD3	GRCh38.p7	17:7900443	GGGTAGTTGGCAGAG[A/T]TGAGAGGTGGAGCAG	1107
rs776665863	snp	C/T	1.64836e-05	0.0028708	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903013	TCTGGCCACTGCTGA[C/T]ACTGTCATCATCTTT	1107
rs776666859	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7895744	GTCTCCGTTAGCTTC[C/T]TTCCCTCAGATATAG	1107
rs776712947	snp	A/G/T	6.72556e-05	0.00579861	missense	CHD3	GRCh38.p7	17:7910910	TTCAGCGCCGCACCC[A/G/T]TAGGGGCCCTGGCCG	1107
rs776718247	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7896855	GTAGAGACGGGGTTT[C/T]GCCATGTTGGCCAGG	1107
rs776732938	snp	A/G	3.44448e-05	0.00414984	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911619	CTTCACCCAGGCCCC[A/G]TCCCCGAGGCCGACC	1107
rs776791942	snp	C/T	3.9374e-05	0.00443683	intron-variant	CHD3	GRCh38.p7	17:7889822	AAGGCTCAAGAGACC[C/T]ATTCTCAGAGACCTA	1107
rs776847662	snp	A/G	9.88549e-05	0.00702977	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905052	GGCCTCAGCATGGGC[A/G]TATCCCGAGAGCCCT	1107
rs776853409	snp	A/G	1.64738e-05	0.00286995	missense	CHD3	GRCh38.p7	17:7908734	GACATCCAGAATGAT[A/G]CTCAATTTGCCATTA	1107
rs776877158	snp	A/G	0.000671817	0.0183155	missense, intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7884933	GCGGCCGACGAGGAC[A/G]ATGAGGAGGACGACG	1107
rs776885049	in-del	-/C			utr-variant-3-prime	CHD3	GRCh38.p7	17:7911747	TCTCTTCAAGAAGGG[-/C]CCCTTTGTCTTTCTC	1107
rs776906050	snp	A/G	1.70734e-05	0.00292172	intron-variant	CHD3	GRCh38.p7	17:7894901	TCTGTCTGTGTGTCT[A/G]TCCTTGGCCCCCTAG	1107
rs776936266	snp	G/T	1.64765e-05	0.00287019	synonymous-codon	CHD3	GRCh38.p7	17:7903919	TGCAACTGAGGACAC[G/T]GACGTGCAGAACATG	1107
rs776971795	snp	A/G	3.36016e-05	0.00409874	missense	CHD3	GRCh38.p7	17:7901268	AAACTCCCCAGTGGG[A/G]CTTATGAGGGTGGGG	1107
rs777027503	snp	A/G/T	1.65244e-05	0.00287436	intron-variant	CHD3	GRCh38.p7	17:7907565	CAGGGGATGAGGGTA[A/G/T]CATCCTCCCTTCCTA	1107
rs777046567	snp	A/C			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884331	GTTGTTTTAAAAATA[A/C]TTTCAAGGCGGCCAT	1107
rs777077851	snp	A/G	6.09762e-05	0.00552127	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890641	GTGGGGGCAGTGAAT[A/G]TGGAACCGGACCGGG	1107
rs777124929	snp	A/G			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905346	AACTTCGGTGTGTGT[A/G]ACCACATAGGCTAGA	1107
rs777160422	snp	C/T	0.000197664	0.00993947	intron-variant, missense	CHD3	GRCh38.p7	17:7889059	ATGACCAGCTGAGGA[C/T]TTCTTTTCCTCCAGG	1107
rs777166105	snp	C/T	1.7468e-05	0.00295528	synonymous-codon	CHD3	GRCh38.p7	17:7898595	TTCTCCCACTAATGA[C/T]GTGAGTCCTCTCAGT	1107
rs777166270	snp	C/T	1.77505e-05	0.00297908	intron-variant	CHD3	GRCh38.p7	17:7901405	TAGCTGTCTTTACAT[C/T]TGCTTCCTCTTCCCT	1107
rs777179750	snp	A/T	1.93396e-05	0.00310957	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7889733	GAGGACCCAAGAAGC[A/T]GAAGGAGAACAAGCC	1107
rs777210278	snp	A/G/T	0.00012022	0.00775226	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906128	AATACTTCCTGGCTC[A/G/T]ATTTCCTGGGGGGTG	1107
rs777223400	in-del	-/TG			downstream-variant-500B	CHD3	GRCh38.p7	17:7912777	CTCTGTTATTTTTTA[-/TG]GGGGGGGGGAGTTTT	1107
rs777263214	snp	A/G	1.68046e-05	0.00289862	intron-variant	CHD3	GRCh38.p7	17:7894065	GCCAAAGGCCTGGGG[A/G]GGGCGTAGAATGAAG	1107
rs777268484	snp	C/G	1.64806e-05	0.00287054	missense	CHD3	GRCh38.p7	17:7900365	TTGCAGAATAATCTG[C/G]AGGAGCTCTTCCATC	1107
rs777268578	snp	C/T	8.23866e-05	0.00641767	missense	CHD3	GRCh38.p7	17:7903881	AATGAGGCCATCGCT[C/T]GGCTGTTGGACCGGA	1107
rs777278551	in-del	-/A			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904918	GGGCGGTGAATGGAG[-/A]ATGGTGTAGGATATG	1107
rs777326117	snp	C/G/T	0.000138017	0.00830598	synonymous-codon	CHD3	GRCh38.p7	17:7909250	CCACGCCCGCTTCGC[C/G/T]GAGGCCGAGTGCCTG	1107
rs777349451	snp	C/T	3.31532e-05	0.0040713	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903295	CCGGGCTCATCGGAT[C/T]GGCCAGGCCAACAAA	1107
rs777405455	snp	A/G	8.25484e-05	0.00642397	missense	CHD3	GRCh38.p7	17:7911559	AAGGAGCCCCGAGCC[A/G]GGGAGGTGATCTGTA	1107
rs777414277	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7896613	TTTCTCCATGTTGAT[C/G]AGGCTGGTCTCGAAC	1107
rs777453055	snp	C/G	1.74464e-05	0.00295345	missense	CHD3	GRCh38.p7	17:7893500	TCCGGACCCCCCGCC[C/G]TTCCACCACCCCCTG	1107
rs777506442	snp	A/G	1.65108e-05	0.00287317	synonymous-codon	CHD3	GRCh38.p7	17:7907244	GGAGAAGATGGAGAC[A/G]GAGGTGTGTGGCTCC	1107
rs777543731	snp	A/G	8.23852e-05	0.00641762	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905054	CCTCAGCATGGGCAT[A/G]TCCCGAGAGCCCTCC	1107
rs777563005	in-del	-/T	0.00102384	0.0226025	intron-variant	CHD3	GRCh38.p7	17:7907586	TCCCTTCCTATCCCC[-/T]ACCCCCTCCCACAGC	1107
rs777594722	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7891220	TCAGGGAACTCCTAG[A/G]CTCATAAGGATCCAA	1107
rs777609556	snp	A/G	1.67103e-05	0.00289048	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906189	AGCCTAGAGTAGAGG[A/G]GCCAGGCATCCTCCC	1107
rs777647760	snp	C/T	1.75529e-05	0.00296246	intron-variant	CHD3	GRCh38.p7	17:7894658	GGAACCCACCCATCT[C/T]TTTCCCCCTTGGTTT	1107
rs777649816	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7892273	GGTCTGACTCTTTCA[C/T]ACTCCGTCCTACGGA	1107
rs777652324	snp	A/G	2.1002e-05	0.00324046	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890606	TTCTGAGCGAGATGA[A/G]TACCGGGAGAAGTCA	1107
rs777716402	snp	C/T	1.64931e-05	0.00287163	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906539	AACCCTCCTCCCACT[C/T]CCATGCTCCTTAGGG	1107
rs777721188	snp	C/T	1.68173e-05	0.00289972	intron-variant	CHD3	GRCh38.p7	17:7898981	GCCGCCGACTATTTC[C/T]TTGAGCTTTCTGACT	1107
rs777737440	snp	C/G/T	3.30171e-05	0.00406296	stop-gained, synonymous-codon	CHD3	GRCh38.p7	17:7894964	GGAAGAAGAAGAATA[C/G/T]GAAGAGGAGGGAGAG	1107
rs777766454	snp	G/T	9.92769e-05	0.00704476	missense, intron-variant	CHD3	GRCh38.p7	17:7895384	ATCCTACATTGGCGG[G/T]GGGGGGAGCCACCTG	1107
rs777856397	snp	A/C	1.6473e-05	0.00286988	missense, intron-variant	CHD3	GRCh38.p7	17:7895457	TCCCACCCCCCCGTC[A/C]TCTTCAAGGCAGATC	1107
rs777856475	snp	C/T	1.64795e-05	0.00287045	missense	CHD3	GRCh38.p7	17:7893835	GGCGGAGTAAGAGCC[C/T]CCGAGTGCCTGATGG	1107
rs777892088	in-del	-/T	1.7025e-05	0.00291757	intron-variant	CHD3	GRCh38.p7	17:7910334	CTCTTTTTCTGCCTG[-/T]TATCTGTCCATCTGA	1107
rs777898658	snp	C/T	0.000355556	0.0133286	intron-variant	CHD3	GRCh38.p7	17:7904119	CTCAAACAACTTCTT[C/T]GTCTAATAGGTGAGA	1107
rs777959330	snp	C/G	0.000102676	0.00716433	intron-variant	CHD3	GRCh38.p7	17:7895196	CTGTCAGGCCTGATC[C/G]CTTCCCCCATCCCTG	1107
rs777999827	snp	C/T	1.68224e-05	0.00290016	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904427	CCAGTGTTCATTCAT[C/T]CTGTTGCCCTTCAGA	1107
rs778076197	snp	A/C	1.66081e-05	0.00288163	missense, synonymous-codon	CHD3	GRCh38.p7	17:7910851	CTCTGTTCCAGGCCT[A/C]CCCGCCGGGTCCCTA	1107
rs778101474	snp	A/G	1.66252e-05	0.00288311	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903072	TCCAGGTGGGAACTC[A/G]CATCCTAGAACCCCT	1107
rs778123554	snp	A/C/T	6.60637e-05	0.00574701	missense	CHD3	GRCh38.p7	17:7894217	CCTGATGGCCCTGTC[A/C/T]GCACCAAGAAACTAA	1107
rs778170114	snp	C/T			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7888491	TTGGTAGGGGAGGGA[C/T]GTGAACCAGAGCCCC	1107
rs778182369	snp	A/C	1.66012e-05	0.00288103	missense	CHD3	GRCh38.p7	17:7907980	GAAAAGACAGAGAAG[A/C]CCCGGTTCATGTTCA	1107
rs778276008	snp	C/T	2.17228e-05	0.0032956	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905673	AGATAAGCCACTGCC[C/T]CCACTGCTGGCCCGA	1107
rs778300249	snp	C/T	1.65231e-05	0.00287424	intron-variant	CHD3	GRCh38.p7	17:7899318	TCTAGCCTAGACTTA[C/T]GCTGCCCCCATTCTT	1107
rs778337213	in-del	-/AGG	1.65343e-05	0.00287521	cds-indel	CHD3	GRCh38.p7	17:7894944	TCCAGTGGGAGGCCA[-/AGG]AGGAGGAAGAAGAAG	1107
rs778354413	in-del	-/G			downstream-variant-500B	CHD3	GRCh38.p7	17:7912779	CTGTTATTTTTTATG[-/G]GGGGGGGGAGTTTTT	1107
rs778378357	snp	C/T			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886861	CGTTGGGGAGAGAAG[C/T]GTGAAAGGATCCGAG	1107
rs778380973	snp	C/T	1.76833e-05	0.00297344	intron-variant	CHD3	GRCh38.p7	17:7910313	ACATCTGTGTTCTCC[C/T]CTCTCGCTCTTTTTC	1107
rs778390530	in-del	-/GCAGCA	1.96171e-05	0.0031318	cds-indel	CHD3	GRCh38.p7	17:7893415	GTGGCGGCGGCAGCG[-/GCAGCA]GCAGCAGCAGCAGCA	1107
rs778392204	snp	A/G	1.64855e-05	0.00287097	synonymous-codon, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902944	CCTCCTAGCTCCTGG[A/G]GCCCAACAATTCTGC	1107
rs778403329	snp	A/G	1.65127e-05	0.00287334	missense	CHD3	GRCh38.p7	17:7897288	TCCACCGCATCATCA[A/G]CCACAGGTGAATCCT	1107
rs778416335	snp	A/G	3.38633e-05	0.00411467	intron-variant	CHD3	GRCh38.p7	17:7894302	TGATCCTGTCAGTGG[A/G]CCGTCCTCTCATTCT	1107
rs778469949	snp	A/G			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905509	ATTGGGAGCACCTCA[A/G]ACGTGACAGGAATGT	1107
rs778470006	snp	A/G	1.64822e-05	0.00287068	synonymous-codon, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905924	CTGGGGGATGCCACC[A/G]CAGGATGCCTTCACC	1107
rs778471548	snp	A/C	6.61255e-05	0.00574964	intron-variant	CHD3	GRCh38.p7	17:7907268	TGGCTCCCTGGATTC[A/C]CCTGTGGAGCGGGAG	1107
rs778491039	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7891392	TCTTCTGCTCTGTGA[A/C]TTCTCTCTAGACTGG	1107
rs778492255	snp	C/G/T	3.3016e-05	0.00406289	intron-variant	CHD3	GRCh38.p7	17:7900841	TTTTACACCCCTTTC[C/G/T]TGGCCTTTAGGAAAT	1107
rs778494683	snp	A/G	2.4797e-05	0.00352106	synonymous-codon, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890741	AGATGGGGGGCAAAA[A/G]GTGAGTAGAATTAGG	1107
rs778503930	snp	C/T	1.64814e-05	0.00287061	synonymous-codon	CHD3	GRCh38.p7	17:7895105	TTGTCTAAACCCTCC[C/T]CTGCCTGACATTCCC	1107
rs778587762	snp	A/G	1.65362e-05	0.00287538	intron-variant	CHD3	GRCh38.p7	17:7899299	AGGACTAGGGTATAC[A/G]GCCTCTAGCCTAGAC	1107
rs778652413	snp	C/T	0.000102338	0.00715253	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911615	TGCCCTTCACCCAGG[C/T]CCCGTCCCCGAGGCC	1107
rs778672721	snp	C/T	1.64735e-05	0.00286993	intron-variant, missense	CHD3	GRCh38.p7	17:7889070	AGGATTTCTTTTCCT[C/T]CAGGACTGTGTTGGG	1107
rs778673181	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7892643	CTGAGACTACAGGTG[C/T]GCACCACTACACCCA	1107
rs778673390	snp	C/T	1.64806e-05	0.00287054	missense	CHD3	GRCh38.p7	17:7900697	CCAGCCAAGACAGAG[C/T]TCATCGTTCGGGTGG	1107
rs778779035	snp	C/T	5.24031e-05	0.00511848	missense	CHD3	GRCh38.p7	17:7893503	GGACCCCCCGCCCTT[C/T]CACCACCCCCTGCTG	1107
rs778844675	snp	C/T	3.10931e-05	0.00394279	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911676	CCAGCCCTCCACCTT[C/T]CCCACCCCTTGGGCC	1107
rs778845701	snp	A/C	0.000131467	0.00810654	missense	CHD3	GRCh38.p7	17:7909270	CCGAGTGCCTGGCCG[A/C]GAGCCACCAGCACCT	1107
rs778846206	snp	C/T	1.64849e-05	0.00287092	missense, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906573	ATGTGTCTTTGTTCA[C/T]GCGCCATCTGTGTGA	1107
rs778853591	snp	C/T	1.65633e-05	0.00287774	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904452	TTCAGATTGAGGAAA[C/T]TGAGCGAGAGATCAT	1107
rs778862217	snp	G/T	1.67164e-05	0.00289101	intron-variant	CHD3	GRCh38.p7	17:7904017	TTGGGGGCCAGACAT[G/T]ATCTATCCCAGGCCA	1107
rs778872794	snp	C/T	1.84215e-05	0.00303486	intron-variant	CHD3	GRCh38.p7	17:7893607	CTGTCATCTCACCTT[C/T]CAAACTGCATGTCTT	1107
rs778894067	snp	C/G/T	6.61314e-05	0.00574995	intron-variant	CHD3	GRCh38.p7	17:7893951	GTGAGTGACCCGTCC[C/G/T]TGTCTACTAAACACC	1107
rs778951661	snp	A/G			intron-variant, utr-variant-5-prime	CHD3	GRCh38.p7	17:7888912	TAGTTCCCAAAGGGA[A/G]CAGGGAGATGGGAAT	1107
rs778966668	in-del	-/T	1.70627e-05	0.00292079	intron-variant	CHD3	GRCh38.p7	17:7910609	AACCCTCTTTCCCCC[-/T]AGCTCCAGTTTTCCC	1107
rs778986150	snp	C/G	6.58913e-05	0.00573945	synonymous-codon, intron-variant	CHD3	GRCh38.p7	17:7895491	GCGAGAGTTCTTTGT[C/G]AAGTGGGTAGGACTA	1107
rs779049648	snp	C/T	1.75832e-05	0.00296501	intron-variant	CHD3	GRCh38.p7	17:7901213	ATGTTTCCAACTGAC[C/T]CCCTCCTCCTCCTCT	1107
rs779133005	snp	A/C	3.3173e-05	0.00407252	intron-variant	CHD3	GRCh38.p7	17:7900512	GTCTGAGATCAGGGG[A/C]AAGGAACTTGCCGAC	1107
rs779185754	snp	G/T			intron-variant	CHD3	GRCh38.p7	17:7901803	GTATAGCAAGTTCAT[G/T]CTTGGCCTCTGATGC	1107
rs779214257	snp	C/T	3.35216e-05	0.00409386	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910585	CACGGAGCCTCACCC[C/T]ACACCGGTAACCCTC	1107
rs779262703	snp	A/G	1.64789e-05	0.0028704	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890943	CCTCTCCCGCAGCAA[A/G]TGGAACAGAAGTCAT	1107
rs779268870	in-del	-/A	3.3018e-05	0.00406299	intron-variant	CHD3	GRCh38.p7	17:7900252	TCACTTGTCACTAAT[-/A]AGCCCATTTTCCTGC	1107
rs779270848	in-del	-/GT			downstream-variant-500B	CHD3, LOC284023	GRCh38.p7	17:7912995	TTGACTTCAGAGAGA[-/GT]GGGACTTACTGGACA	1107
rs779295383	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7897350	CATTATTCTTACCAT[A/G]GTGATGGCCCCATGT	1107
rs779302301	snp	C/G	1.65239e-05	0.00287431	synonymous-codon, missense	CHD3	GRCh38.p7	17:7910483	GGACGTGACCCGCCT[C/G]CCAGCCACGCTGTCC	1107
rs779318804	snp	C/G	1.69012e-05	0.00290694	missense, synonymous-codon	CHD3	GRCh38.p7	17:7910953	ATTACAGCCAGATGC[C/G]TGCAGGGTCCTTCAT	1107
rs779331791	snp	A/G	4.94491e-05	0.00497213	synonymous-codon	CHD3	GRCh38.p7	17:7906910	GCGTTGGTCAATGCC[A/G]GAACTGATGCCTGAC	1107
rs779370186	snp	A/G	4.94214e-05	0.00497074	missense, intron-variant	CHD3	GRCh38.p7	17:7895399	TGGGGGGAGCCACCT[A/G]TAGCAGTGCCAGCCC	1107
rs779378178	snp	A/G	3.31757e-05	0.00407269	intron-variant	CHD3	GRCh38.p7	17:7910379	TGGCTCCATCTCTGT[A/G]TTTCCCTGTCTTTCT	1107
rs779421756	snp	A/G	1.67329e-05	0.00289243	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903102	TGCACCATTTAGCAA[A/G]GAGATGTGGGTTCAT	1107
rs779472258	snp	A/C	1.69218e-05	0.00290871	splice-acceptor-variant, intron-variant	CHD3	GRCh38.p7	17:7894413	ACCGGGGTATATGAC[A/C]GTCCTGGGCTGTCCT	1107
rs779508209	in-del	-/CTCTGT	1.67579e-05	0.00289459	intron-variant	CHD3	GRCh38.p7	17:7895159	TGCACAGTGAGTGGA[-/CTCTGT]AACATCTCCCCTCTG	1107
rs779528412	snp	A/G	1.68306e-05	0.00290087	intron-variant	CHD3	GRCh38.p7	17:7899563	GACCCTCTACCTCAT[A/G]TCCTCTGAGACCCTC	1107
rs779528801	snp	G/T	1.66452e-05	0.00288484	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903283	GCAGGCCTTTAGCCG[G/T]GCTCATCGGATTGGC	1107
rs779562081	snp	C/T	1.67624e-05	0.00289498	missense	CHD3	GRCh38.p7	17:7894600	GGCAAATGGAGCTGC[C/T]CTCACTGTGTGAGTA	1107
rs779604288	snp	A/G	1.65252e-05	0.00287443	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905959	AGTGGCTGGTGCGGG[A/G]CCTGAGGGGCAAGAC	1107
rs779614832	snp	C/T	1.69055e-05	0.00290731	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7906096	TACTCAACTGATTAT[C/T]ACCCTCCCTGTCATA	1107
rs779704780	snp	G/T	1.64909e-05	0.00287144	synonymous-codon	CHD3	GRCh38.p7	17:7894557	CCACCTCGTCTGCCT[G/T]GATCCTGAGCTTGAC	1107
rs779729693	in-del	-/AC			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884072	CTTCATGCCCCCCCA[-/AC]ACACACACACACACA	1107
rs779749152	snp	A/G			synonymous-codon	CHD3	GRCh38.p7	17:7908403	TGCCTTCTTTGCAGA[A/G]CTTCACACACTGTGG	1107
rs779799071	snp	A/T	3.35182e-05	0.00409365	intron-variant, downstream-variant-500B	CHD3	GRCh38.p7	17:7903107	CATTTAGCAAGGAGA[A/T]GTGGGTTCATGGAGG	1107
rs779803803	snp	A/G	1.76702e-05	0.00297234	synonymous-codon	CHD3	GRCh38.p7	17:7909316	GGCGGGGAACAAGCC[A/G]GCCAACGCCGTCCTG	1107
rs779817792	snp	A/G	1.65715e-05	0.00287845	intron-variant	CHD3	GRCh38.p7	17:7898108	GGAGACACCGGTGAG[A/G]GAATGAGCTTGTGGA	1107
rs779876097	snp	A/C	1.69565e-05	0.00291169	intron-variant	CHD3	GRCh38.p7	17:7910979	TTCATCACAGGTCAG[A/C]TGGTGTTTTCCTACC	1107
rs779882220	in-del	-/GCGGCA	1.839e-05	0.00303227	cds-indel	CHD3	GRCh38.p7	17:7893407	GCAGCTGCTGTGGCG[-/GCGGCA]GCGGCAGCAGCAGCA	1107
rs779900207	snp	C/T	1.70743e-05	0.00292179	intron-variant	CHD3	GRCh38.p7	17:7907346	TGACCCCATTGTCCT[C/T]TTCCAGGCTGATGCC	1107
rs779905716	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	CHD3	GRCh38.p7	17:7900891	TCGAAATTTTGAGGC[C/T]TTGAATTCACGAGGT	1107
rs779968423	snp	C/T	4.17737e-05	0.00457002	utr-variant-3-prime, missense	CHD3	GRCh38.p7	17:7911693	CCACCCCTTGGGCCA[C/T]CACTGGGCTAGGAAC	1107
rs779975301	snp	C/T	1.69481e-05	0.00291098	intron-variant	CHD3	GRCh38.p7	17:7910597	CCCCACACCGGTAAC[C/T]CTCTTTCCCCCTAGC	1107
rs779993369	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7892774	TACTGGGATTACAGG[C/T]GTGAGCCACTGCGCC	1107
rs779994651	snp	A/C	3.37861e-05	0.00410997	intron-variant	CHD3	GRCh38.p7	17:7904040	CCAGGCCATCTCCAA[A/C]AGGCAGTATCCTTTA	1107
rs780011049	snp	A/G	0.000724838	0.0190235	intron-variant	CHD3	GRCh38.p7	17:7889622	GGCCTCAGAGGCTGG[A/G]AACCTAGAGGCTTAG	1107
rs780031680	in-del	-/T			intron-variant	CHD3	GRCh38.p7	17:7892498	TTTTTTATTTCCCCT[-/T]TTTTTTTTTTTTTTT	1107
rs780103840	snp	C/G	1.64727e-05	0.00286986	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905111	ACAGACAACCAGTCA[C/G]AGTACTCGGTGGGTT	1107
rs780105859	snp	A/G	1.75394e-05	0.00296132	intron-variant	CHD3	GRCh38.p7	17:7901395	CCTGTGCCCTTAGCT[A/G]TCTTTACATCTGCTT	1107
rs780115167	snp	A/G	1.6671e-05	0.00288708	intron-variant	CHD3	GRCh38.p7	17:7894103	CACTGACGGCCACGG[A/G]GCTATGGGCAGTATG	1107
rs780160021	snp	C/G			intron-variant	CHD3	GRCh38.p7	17:7904086	GGAGGGTCTGTCCCC[C/G]TTAAAACAGTAGTGG	1107
rs780165447	in-del	-/CGTTC	1.65176e-05	0.00287376	intron-variant	CHD3	GRCh38.p7	17:7900782	GGGGATTGATGGGAG[-/CGTTC]CAAGTGCAATATCAT	1107
rs780192898	snp	A/G	3.38083e-05	0.00411133	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904421	AGACCCCCAGTGTTC[A/G]TTCATTCTGTTGCCC	1107
rs780204966	snp	G/T	1.64746e-05	0.00287002	intron-variant, missense	CHD3	GRCh38.p7	17:7889086	CAGGACTGTGTTGGG[G/T]TGACAGGATGCCTGG	1107
rs780206250	snp	C/G	2.01582e-05	0.0031747	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890628	GAGAAGTCAGAGAGT[C/G]GGGGCAGTGAATATG	1107
rs780265671	snp	C/T	1.80231e-05	0.00300187	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906204	GGCCAGGCATCCTCC[C/T]CAGGGGAGGGGCGTT	1107
rs780284516	snp	C/T	1.64781e-05	0.00287033	missense	CHD3	GRCh38.p7	17:7899177	CCATACAAACCATCG[C/T]CTTCCTCTACTCACT	1107
rs780307323	snp	C/T	1.64787e-05	0.00287038	synonymous-codon	CHD3	GRCh38.p7	17:7902651	GGACTTCTTAGACTA[C/T]GAAGGCTACAAGTAT	1107
rs780326109	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7890033	AGAAGCAGTTGAAAG[C/T]ACAAGCTCTGGAAGA	1107
rs780371866	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7898462	CGTAGGACTCCCAAG[A/G]ATGAGGCCTCATTCA	1107
rs780379002	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7911405	AATTCACCATTGTCA[C/T]GAAGTGACGTTTGAG	1107
rs780429011	snp	A/G			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7883741	GGTATGTAGAAACAG[A/G]GTTATATATAAACAT	1107
rs780443685	snp	C/T	1.66576e-05	0.00288592	intron-variant	CHD3	GRCh38.p7	17:7908550	AGGAAAAGGTTCTCT[C/T]AAGCTGGCAAAAAAA	1107
rs780482986	snp	A/G	5.93055e-05	0.00544511	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904668	GGGAAGTGATGATGA[A/G]TAGGGACTTGAAGGC	1107
rs780494957	snp	G/T	1.68289e-05	0.00290072	intron-variant	CHD3	GRCh38.p7	17:7893967	TGTCTACTAAACACC[G/T]GGGGGCCAAGGATCC	1107
rs780509597	snp	C/G	1.84688e-05	0.00303876	missense	CHD3	GRCh38.p7	17:7893422	GCGGCAGCGGCAGCA[C/G]CAGCAGCAGCTGTAG	1107
rs780568982	in-del	-/ACCTGA	0.000627135	0.0176967	cds-indel, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905959	AGTGGCTGGTGCGGG[-/ACCTGA]GGGGCAAGACTGAGA	1107
rs780573521	snp	C/T	0.000115434	0.00759631	missense	CHD3	GRCh38.p7	17:7899977	GCACTTGGTTCCATC[C/T]GCTGGGCCTGTCTTG	1107
rs780630693	snp	C/T	1.64846e-05	0.0028709	intron-variant	CHD3	GRCh38.p7	17:7911461	TACCCCTTTCCCAAA[C/T]AGCCGCCACCAACGG	1107
rs780667900	snp	A/T	1.64757e-05	0.00287012	synonymous-codon	CHD3	GRCh38.p7	17:7900340	TAAGTTGCTGCTGAC[A/T]GGAACCCCATTGCAG	1107
rs780677674	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	CHD3	GRCh38.p7	17:7897157	GCCCCCACCCCTGGA[C/T]TATGGCTCCGGCGAG	1107
rs780679378	snp	C/T	1.77106e-05	0.00297573	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906172	CCACCTCCCCTCAGC[C/T]GAGCCTAGAGTAGAG	1107
rs780694841	in-del	-/C			intron-variant	CHD3	GRCh38.p7	17:7900234	GCTGATGCTGTGGGT[-/C]GGTCACTTGTCACTA	1107
rs780752390	snp	C/T	3.29891e-05	0.00406122	synonymous-codon, downstream-variant-500B	CHD3	GRCh38.p7	17:7903334	TTACCGGTTTGTGAC[C/T]CGCGCGTCAGTGGAA	1107
rs780818587	snp	C/T	4.94515e-05	0.00497225	synonymous-codon, missense	CHD3	GRCh38.p7	17:7911474	AACAGCCGCCACCAA[C/T]GGCCCTCCAGTGCTT	1107
rs780823319	snp	A/G	3.30371e-05	0.00406417	missense	CHD3	GRCh38.p7	17:7910472	GACATGAAGGCGGAC[A/G]TGACCCGCCTGCCAG	1107
rs780847268	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7894681	CTTGGTTTCACTTAC[C/T]CTCTTCCTGCCCCCA	1107
rs780847391	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7910109	GTTCTGACAACTCCC[C/T]GCCCCCATGTCTTCC	1107
rs780869441	snp	C/G	7.62398e-05	0.00617366	intron-variant	CHD3	GRCh38.p7	17:7903539	TCTGTGAAAGCAGGC[C/G]CCTGCTCTCTCAGGA	1107
rs780876995	snp	A/G	5.15548e-05	0.00507688	intron-variant	CHD3	GRCh38.p7	17:7894636	TGCCAGCATCTGATG[A/G]CCCTGAGGAACCCAC	1107
rs780898736	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7896594	ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT	1107
rs780922828	snp	A/G	0.000232211	0.0107727	intron-variant	CHD3	GRCh38.p7	17:7908840	TCAAGGTGGGAATGA[A/G]GGAGGAAAGGAGCGG	1107
rs780939883	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7890168	GGTTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	1107
rs780940251	in-del	-/C			intron-variant, upstream-variant-2KB	CHD3	GRCh38.p7	17:7887544	GAAAATACAAACCCA[-/C]CCCCCTGCCTGCAGT	1107
rs780964961	snp	C/T	3.77943e-05	0.00434692	missense	CHD3	GRCh38.p7	17:7893462	TGTCAGCTGCTGTCT[C/T]GTCGGCCACCCCCAT	1107
rs781012905	snp	C/T	4.94898e-05	0.00497418	intron-variant	CHD3	GRCh38.p7	17:7908650	GTGTTCAAAGCCAAG[C/T]CCATTCCTGTTAAAT	1107
rs781033971	snp	A/T			stop-gained	CHD3	GRCh38.p7	17:7899457	ACATACACGGGTGAC[A/T]AGGACAGCCGGGCCA	1107
rs781050291	snp	A/G	0.000134014	0.00818469	intron-variant	CHD3	GRCh38.p7	17:7889787	AGCGTGTAAGTGTCA[A/G]GAATTCCTAACTCTG	1107
rs781081716	snp	C/T	3.30218e-05	0.00406323	intron-variant	CHD3	GRCh38.p7	17:7893946	GCTCGGTGAGTGACC[C/T]GTCCCTGTCTACTAA	1107
rs781107745	snp	C/T	1.82304e-05	0.00301908	intron-variant	CHD3	GRCh38.p7	17:7907842	ATAGTAGTCTTGGGA[C/T]CTGGGAGGAGGGTGT	1107
rs781122260	snp	C/T	4.22592e-05	0.0045965	intron-variant	CHD3	GRCh38.p7	17:7907598	CCCTACCCCCTCCCA[C/T]AGCCACAGAGTCGAC	1107
rs781135209	snp	A/G	1.80739e-05	0.0030061	intron-variant	CHD3	GRCh38.p7	17:7907507	GGTGCATGGCCTTAG[A/G]AGTGATGGGGGATTA	1107
rs781136749	snp	C/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7904982	GTGTTCCCAGAAGGA[C/T]CAAGGCCAGAATAAA	1107
rs781153088	snp	C/G	9.63005e-05	0.00693837	intron-variant	CHD3	GRCh38.p7	17:7889649	TTAGGTTTTCTGATG[C/G]TTTTTGCTTCAAAGA	1107
rs781196519	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7891142	CCTTGGAATCTGATG[A/G]AAGCTATGAAACTGC	1107
rs781214124	snp	A/G			downstream-variant-500B	CHD3, LOC284023	GRCh38.p7	17:7913011	TGGGACTTACTGGAC[A/G]GAAATGTAGTGGGAG	1107
rs781238793	in-del	-/G	5.16814e-05	0.00508311	intron-variant, nc-transcript-variant	CHD3, SCARNA21	GRCh38.p7	17:7906136	CTGGCTCGATTTCCT[-/G]GGGGGTGGTCTCAGC	1107
rs781256029	snp	A/G	1.64958e-05	0.00287187	intron-variant	CHD3	GRCh38.p7	17:7899208	CTACAAGGAGGTGCT[A/G]GATTCTAGGACCTTG	1107
rs781256088	snp	A/C	1.65086e-05	0.00287298	intron-variant, utr-variant-3-prime	CHD3	GRCh38.p7	17:7902927	ACCTGATCCAACTCT[A/C]ACCTCCTAGCTCCTG	1107
rs781332946	snp	A/C			intron-variant	CHD3	GRCh38.p7	17:7897568	GGATGAGGGCATGAA[A/C]GCAAAACATGAGAGA	1107
rs781335877	snp	A/G	3.32336e-05	0.00407624	missense	CHD3	GRCh38.p7	17:7901332	TCCAGAAGATGCTGC[A/G]AAAGCTGAAGGAGCA	1107
rs781353736	in-del	-/GAG	0.308371	0.24309	cds-indel, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884828	TCCCCTCTGAGGGAC[-/GAG]GAGGAGGAGGAGGAG	1107
rs781361149	snp	A/T	1.65026e-05	0.00287246	missense, synonymous-codon	CHD3	GRCh38.p7	17:7911548	GGCTGGATCGGAAGG[A/T]GCCCCGAGCCGGGGA	1107
rs781363200	snp	A/G	6.68393e-05	0.00578059	intron-variant	CHD3	GRCh38.p7	17:7895153	TCCCCGATGCACAGT[A/G]AGTGGAAACATCTCC	1107
rs781405222	snp	A/C			intron-variant, upstream-variant-2KB, missense	CHD3, NAA38	GRCh38.p7	17:7887072	ACACCCCCTCAGATG[A/C]CTTTCGGAGGTAAAA	1107
rs781451571	snp	A/C	1.65296e-05	0.00287481	intron-variant	CHD3	GRCh38.p7	17:7899308	GTATACGGCCTCTAG[A/C]CTAGACTTATGCTGC	1107
rs781499738	in-del	-/ACATGGGTGGGGAG	1.68963e-05	0.00290652	intron-variant	CHD3	GRCh38.p7	17:7901039	GCCCATTCTCAGAAA[-/ACATGGGTGGGGAG]ACATGGGTGGGGAGT	1107
rs781505134	snp	C/T	3.28057e-05	0.00404991	intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905612	AACTGATGTCATCCC[C/T]ACCCTCAGGGCGTAG	1107
rs781506178	snp	A/G	3.30797e-05	0.00406679	missense	CHD3	GRCh38.p7	17:7907960	GGTCCAATGGGCGAC[A/G]AGAGGAAAAGACAGA	1107
rs781509760	snp	A/G	1.74166e-05	0.00295093	intron-variant, downstream-variant-500B	CHD3, SCARNA21	GRCh38.p7	17:7906719	GTCTTCCTGTCACCC[A/G]AAGAATCAAGCTGGC	1107
rs781531230	snp	A/G			intron-variant	CHD3	GRCh38.p7	17:7898875	GGCTGAAGACTAGAT[A/G]TGAGAACTTTTGTAA	1107
rs781534324	snp	A/C	2.50153e-05	0.00353653	missense, utr-variant-5-prime	CHD3	GRCh38.p7	17:7890712	AAGACAAAGCGGCGG[A/C]AAAAGGGGGAGGGAG	1107
rs781584045	snp	A/G			upstream-variant-2KB, intron-variant	CHD3, NAA38	GRCh38.p7	17:7884194	GGCTTGGAGATGGGG[A/G]TGTAACAGGGAGGAG	1107
rs781610390	snp	A/T	1.64846e-05	0.0028709	missense	CHD3	GRCh38.p7	17:7907140	GCTACTCCAGCTCCA[A/T]GTGAGAAAGGAGAAG	1107
rs781634549	snp	C/T	1.65209e-05	0.00287405	intron-variant, utr-variant-5-prime	CHD3	GRCh38.p7	17:7888955	AGGTTTTAGGCTACT[C/T]GGGAGGAGGAATATT	1107
rs781636257	snp	A/G	8.31884e-05	0.00644882	intron-variant	CHD3	GRCh38.p7	17:7894109	CGGCCACGGGGCTAT[A/G]GGCAGTATGTTTTTC	1107
rs781637344	snp	C/T			intron-variant, upstream-variant-2KB	CHD3, NAA38	GRCh38.p7	17:7886583	GTGTCTCCTGGAAAC[C/T]GGATAAAGTCTCCCC	1107
rs781700602	snp	C/T	3.29489e-05	0.00405874	synonymous-codon	CHD3	GRCh38.p7	17:7897166	CCTGGACTATGGCTC[C/T]GGCGAGGATGATGGG	1107
rs781708538	snp	A/G	1.65141e-05	0.00287346	missense	CHD3	GRCh38.p7	17:7894209	CAGGCCGGCCTGATG[A/G]CCCTGTCCGCACCAA	1107
rs781745065	snp	C/G	1.64727e-05	0.00286986	missense, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905129	TACTCGGTGGGTTCA[C/G]AGGAGGAGGATGAAG	1107
rs781755922	snp	C/G	1.64933e-05	0.00287165	missense	CHD3	GRCh38.p7	17:7897270	AGCCAGAGTGGATGA[C/G]CGTCCACCGCATCAT	1107
rs796191267	snp	A/T			intron-variant, upstream-variant-2KB	CHD3, SCARNA21	GRCh38.p7	17:7905538	GTTCCTGTGTTGTGT[A/T]TCTTGTGGGAATGGG	1107
rs796911315	snp	C/T			intron-variant	CHD3	GRCh38.p7	17:7890287	AATACAAAAATCAGC[C/T]GGGCGCGGTGGTACG	1107

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