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

KLHL28

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs377423129	snp	A/G	4.94507e-05	0.00497221	missense, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929063	AGTTGCAGCGACAGT[A/G]TATCATGCCAGCTGA	54813
rs377453437	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44951833	CACTAGCAGTTTTCC[A/G]TAACATAATTTTTTT	54813
rs377496566	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44973365	AACCCAAGTACCTTA[C/T]AATAACAGAATATTT	54813
rs377577087	snp	C/T	3.29663e-05	0.00405981	missense	KLHL28	GRCh38.p7	14:44934230	GTTGCCATTTTCTTA[C/T]TTTGGGAATGTACTT	54813
rs377582876	snp	A/C	0.215747	0.247642	intron-variant	FAM179B	GRCh38.p7	14:44973594	tctctctctctctat[A/C]tatatatatacatat	54813
rs377628301	in-del	-/AACA			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926052	GAGGATTTATAACCA[-/AACA]TTTTGATCCTTTTTA	54813
rs377664199	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44944514	GTCTTTTAAAAATAC[A/G]CTGAAGAAAACAAAT	54813
rs377726724	snp	A/G	0.00176871	0.0296855	intron-variant	KLHL28	GRCh38.p7	14:44931550	CTCCACACTGCAAAT[A/G]TTTAAAAAAAATTTA	54813
rs386777020	multinucleotide-polymorphism	CGA/TGG			intron-variant	KLHL28	GRCh38.p7	14:44931041	ATGACATTTGTTACA[CGA/TGG]ACAAAAGGAGCTTCT	54813
rs386777021	multinucleotide-polymorphism	AC/CT			intron-variant	KLHL28	GRCh38.p7	14:44940190	GATAACTAACCTACT[AC/CT]CACAATAATAGCATT	54813
rs386777022	multinucleotide-polymorphism	ATT/TTA			intron-variant	KLHL28	GRCh38.p7	14:44947057	CTGGAATCTGTGAAT[ATT/TTA]ACTTTATATGGCAAA	54813
rs386777023	multinucleotide-polymorphism	ATG/GTA			intron-variant	KLHL28	GRCh38.p7	14:44955657	TGGATGTGGTGGCAC[ATG/GTA]CCTGTAGTCTCAGCT	54813
rs386777024	multinucleotide-polymorphism	AA/GC			intron-variant	KLHL28	GRCh38.p7	14:44956158	AAGAGATAGGGTCTT[AA/GC]TACCTTGCCGAAACT	54813
rs386777025	in-del	ATA/TC			utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961011	CTTCAAAAAAAAAAA[ATA/TC]TCTCTTCCACACTCC	54813
rs397707333	in-del	-/T	0	0	intron-variant	FAM179B	GRCh38.p7	14:44977252	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC	54813
rs397729283	in-del	-/AAAAC			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960744	AAAACAAAACAAAAC[-/AAAAC]TGATATTCAAATCGT	54813
rs397784288	in-del	-/T	0.375	0.216506	intron-variant	KLHL28	GRCh38.p7	14:44933328	CTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC	54813
rs397853101	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44949748	CCAAACCAACTACCC[-/C]AAGTATAGAATAAGA	54813
rs397968833	in-del	-/A			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928705	AAAAAAAAAAAAAAA[-/A]GCAGCCACGTTTTGT	54813
rs527255914	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957015	TTTTTTGTAGAGATG[A/G]GATCTCACTATTTGT	54813
rs527273333	snp	A/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44965422	TCTAGAATAATATCC[A/T]ACTTGTTTGTTTCTT	54813
rs527436953	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957998	AGGATCCATGGAACA[A/C]TCATTGCCTTCCAGT	54813
rs527534982	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971691	GCCTTCAGTGCCATA[A/G]ATTTCCTCTAGGCAC	54813
rs527621283	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947305	AGAACAGATTCTCCC[A/G]TAGAGCTTATGGAAG	54813
rs527737036	snp	C/T	0.0023933	0.0345097	intron-variant	FAM179B	GRCh38.p7	14:44966237	AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATAA	54813
rs527737522	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44973612	TATATATACATATAT[A/G]TATATCTCTCTCCAG	54813
rs527800895	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925792	GCAATAACACAATTT[A/G]TAAATATCCTTGGAG	54813
rs527854259	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44950594	TTTGTATGATATGCA[A/G]TATAGTTTTAAGAGA	54813
rs527882418	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942871	TTATGTATTATTTTC[C/T]ACATGTCTCCTTTAC	54813
rs528020779	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44965477	TATAAAAAGAGTTTG[A/G]GGTAGTTTTGTAGAA	54813
rs528050424	snp	A/C	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44929252	AGTATACTTTTTCTC[A/C]CTAAAAATAAATTTG	54813
rs528080246	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975942	ATAAAATCTTCTTAG[C/T]GAAGTCAACTGGTGA	54813
rs528245708	in-del	-/TGAGCCAC	0.00119737	0.0244387	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926789	CTGGGATTACAGGCG[-/TGAGCCAC]TGCGCCCGTCCTAAA	54813
rs528260248	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944916	AAAAAAACTAAAAAG[A/C]AGCAAAGAAAAGTAA	54813
rs528263764	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44964527	AATGAAAATATGCCC[G/T]TGATGACTTAAGGGT	54813
rs528281475	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44931286	GCAAGCACATCATTA[C/T]AGAAAACATTGCCTT	54813
rs528292293	snp	A/G	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44953145	AAAATATAAAAGTAG[A/G]TCATTTAGATATGCA	54813
rs528311539	in-del	-/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928684	GAAGGAGAGCTAAAA[-/T]AAAAAAAAAAAAAAA	54813
rs528392963	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44938608	ATCTCCTGACCTCGC[A/G]ATCTGCCCGCCTTGG	54813
rs528422031	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937661	AGTTCATTTTCTGCC[A/G]ATATAACAGAATACT	54813
rs528439584	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44947529	TACAGGTCATGTATA[C/T]AATATAAGCTATTTC	54813
rs528552883	snp	C/T	3.32436e-05	0.00407685	missense, intron-variant	KLHL28	GRCh38.p7	14:44931351	TTCTAGGTTCTTTCA[C/T]TGGTCTACACACAGT	54813
rs528555035	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940774	TCCTCTAAGATCTTG[C/T]TTCATCAATAAGCAT	54813
rs528677538	snp	A/T	0.000184056	0.00959135	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962726	CTCGGCTCCTTCAAC[A/T]CCTCCGCACTGCCCG	54813
rs528691148	in-del	-/TTAT	0.0126979	0.078662	intron-variant	KLHL28	GRCh38.p7	14:44952756	TATATTTGGTTCTCA[-/TTAT]GCTATCTACCCATAA	54813
rs528712252	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970013	TTCCATGTTGAGTTC[A/T]CTCTTCTGGGTTTTT	54813
rs528793673	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44969433	CTGGGATTACAGGTG[C/G]AAGCTACCACGCCTG	54813
rs528824017	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955063	AAATGAGTAATGATA[C/T]GATATTCTATCAACC	54813
rs528841688	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44976569	ACAGGAGGCACTTGA[A/C]GATGTTTGTTCAGTG	54813
rs528954320	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943954	CTCCAGTCTCAAGTG[A/T]TCCTCCTGTGTTGGC	54813
rs528990282	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943272	CCAGTGCATTTCAGA[A/T]TAAGAGTTAAACAAT	54813
rs529019839	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44943650	CAACAAAAGCCAAAC[G/T]CTGTATCAAAAAAAT	54813
rs529055160	in-del	-/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937474	GTTAAATACCTAGTT[-/G]ATGTCAGAGAATTGG	54813
rs529219216	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959190	CACCAAAACCTTCTC[C/T]AAGCTCTAAGCAAAT	54813
rs529229925	snp	C/T	0.0023933	0.0345097	intron-variant	FAM179B	GRCh38.p7	14:44968503	TCTGCCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG	54813
rs529249646	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966752	TGAGGCCAGGAGTTC[A/G]AGACCAGCCTGGGCA	54813
rs529267652	snp	A/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44967726	AGATGTAGATGGGGT[A/G]AAGTATGGAGATAAT	54813
rs529277389	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44938431	GGCTGGAGTGCAGTG[C/G]TGCAATCTCGGCTCA	54813
rs529414805	snp	C/T	0.00062729	0.0176989	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963312	TCAATCTTACATTTC[C/T]CGTCTGCCCTCTGCC	54813
rs529430238	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961507	CAAAAAAAAATTAAC[A/C]CTCTGCGGCCGGAGG	54813
rs529499265	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44974482	GTTAACTTCAACATT[C/T]CTGCCATATCCAATT	54813
rs529522815	snp	C/T			intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937678	TATAACAGAATACTA[C/T]AGACTGGGTAATTTA	54813
rs529558643	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44970295	ATCCTACTTCTGTAT[A/G]TTAATGTAAATGGTA	54813
rs529613436	in-del	-/A			utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961000	TAGTATTATTCCTTC[-/A]AAAAAAAAAAATATC	54813
rs529613665	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926994	AAAGTCTGGGCCAAC[C/T]ACAATAGTGCACCTA	54813
rs529619383	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944433	TTTACTGTTTGGTCT[C/T]TTATAGAAAAAGTCT	54813
rs529625193	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971615	TTGCTCTTCCTTTGT[C/T]AGTTTCCTAGGATGT	54813
rs529626649	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972759	ATTTATATCTATCTT[C/G/T]ATATTTAAAATGGGT	54813
rs529649671	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935672	CAAAATTATAATGAA[A/G]AGCAAGGGAATAGTT	54813
rs529661170	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970820	TCTTCTTAAACCTGA[A/T]GATGTGATGGGTTAT	54813
rs529795422	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44964770	AACAAACATTGAATA[C/T]CTAGTACGTGCCAGA	54813
rs529807946	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940029	CTTTCAGTTTTGGGG[G/T]CTGTAAAGTCCAAGA	54813
rs529855719	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44930353	AGAGTGCAGTGGCGC[A/G]ATCTCGGTTCTAGCG	54813
rs529964870	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931224	CTTTTTTTTTTTTTT[C/T]CTGGACAAGTAATAT	54813
rs529979514	snp	A/C	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44977525	ACAGGCGTGAGCCAC[A/C]GCACCCGGCCAAGAC	54813
rs530005368	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44932758	TAAAATACTTAACCT[A/T]TTATCTTACAAATTT	54813
rs530160231	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	KLHL28	GRCh38.p7	14:44923930	GCTGGAATGCAATGG[C/T]GCCATCTCGGCTCAC	54813
rs530196508	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924854	GACATATGGATAACA[A/G]TTTTTCTCTCTGCAG	54813
rs530206502	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44946269	TCAAGTCTGAGCTAT[A/C]ACTGAAATAAAATGA	54813
rs530236431	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44934011	AGTTTCCCAAATGCC[A/G]GAAGTTCATTCATAC	54813
rs530238133	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44956914	CCTTGAATTCCTGGG[C/T]TCAAGGGATTCTCCC	54813
rs530283952	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957520	CAATGTTGAGCTGCT[G/T]AAAATATTTACTGAA	54813
rs530413999	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44938377	GAAAACATTGTCTTC[-/T]TTTTTTTTTTTTGAG	54813
rs530450069	snp	A/C	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44949310	GGATATATGAGCTAA[A/C]AATAATAAGACATGT	54813
rs530522416	snp	A/G	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44930744	TTTTGGATAGGAAAT[A/G]TTCAATCTGTATGAG	54813
rs530578889	snp	C/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44975250	CAATGGATGCCCCCC[C/G]ACCAGGTGAAAGCCT	54813
rs530782970	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954948	ATTGCGACATGCCCT[A/G]AAATATATATCTTAT	54813
rs530818170	snp	A/T	3.32502e-05	0.00407725	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962564	GAGGAGAGAAAAACT[A/T]CTACTTCCGTGGAGC	54813
rs530819845	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954447	AAAACAACTCTCATG[C/T]CCAGCAACAAAAGAA	54813
rs530863136	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953096	CAGGATTAAATGAGA[C/T]GTATGTAAGGAAAAA	54813
rs530904826	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44964897	TGCTAAAGTAGAAAT[A/G]TAAAGAGTCCTGCAG	54813
rs530907251	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947360	TTAGCCCACTGACAC[A/G]AATTTCAGACTTCTG	54813
rs530940464	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44931685	CACAAATGCTTAGGT[C/T]TTGCTGATAAGATTG	54813
rs530943696	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946847	AGGCATGGGCCACCA[C/T]ACCCGGCCTCAACTC	54813
rs531032853	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968670	TCCGGTACTTTAGGG[G/T]TACATTTGTTATAAT	54813
rs531155227	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969823	TCTTTACTCCATTGC[C/T]TTTACTTCTTTGTCA	54813
rs531174786	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944081	GAAAGGGAAAAGCAA[C/T]CTACCAAATTTTTGG	54813
rs531179916	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958816	TAGTAATTAATATGT[A/G]ATACAAGTTGGATTT	54813
rs531281925	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962267	TTTGCCAGAGGCTGC[C/T]TCCCGGAGTTGGGGG	54813
rs531301725	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942296	AATCCTGTCAATTTA[A/C]TCTGTTAAAACATTT	54813
rs531333377	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44977977	TGAAAAGAACTGGGC[A/G]GCACCACGTGAGCTG	54813
rs531340362	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950661	AATGGTCTGTATTAT[C/G]TGACCTTGGGAAATT	54813
rs531348937	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966002	ACCTCAGTGTCCTGA[C/G]TAGCTGAGATTACAG	54813
rs531391342	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972185	ATTTGGGACAGGATA[C/G]AAACCCAAACCATAT	54813
rs531510931	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44979257	TTAGACTGGGTAATT[C/T]ATAAACAATAGACAT	54813
rs531545327	in-del	-/T	0.0267878	0.112589	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928688	AGAGCTAAAATAAAA[-/T]AAAAAAAAAAAAAAA	54813
rs531555190	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44965514	AAGTTTTACATTTAT[A/T]TGTTTACTTGATTAG	54813
rs531593676	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967092	GGGCAGTGGTATTTG[A/G]AAACAAAAGTCTGAG	54813
rs531617869	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44973623	ATATATATATCTCTC[C/T]CCAGGTTTTTGACCT	54813
rs531667129	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44978987	TCTTTTTTTTTTTAA[C/T]GTCACTAACCAATCC	54813
rs531794647	snp	A/C/G	1.64846e-05	0.0028709	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964265	CGGACTGGCTTTTGG[A/C/G]TGGTAACAGAACTCA	54813
rs531817184	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44938533	CCCACCACCACGCCC[A/G]GCTAATTTTTGTATT	54813
rs531881665	snp	A/C	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44967588	CCAGTGAATTTCAGA[A/C]TAAAGGAATAGCGTG	54813
rs531890196	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959996	AAAATAACTCTAAAA[G/T]ATAATCAGTAAGACG	54813
rs531891900	snp	A/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44943148	TAATTTGTTATTTTT[A/T]ATAGTTGAGAAAATA	54813
rs532024072	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977492	CTGCCCGCCTTGGCC[A/T]CCCAAAGTGCTGGGA	54813
rs532025525	snp	G/T	0.00119737	0.0244387	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925906	AATTATAGAAGGCAA[G/T]TATCTTGCAACTGAT	54813
rs532063484	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924959	TGTATTGTATTCCTC[A/T]CTCTTTTCAAATGTG	54813
rs532117500	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44949664	GACTAACACAATAAG[A/G]ATCCTGAAAGACTTA	54813
rs532121893	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44970054	TATAAACTTTAGAAT[C/T]AGTTTGTTGATGTCC	54813
rs532141932	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44955578	CCCAGGAGTTTGAGA[C/T]CAGCCTGGGCAACAC	54813
rs532180695	snp	A/C	0.000118828	0.00770714	missense, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44960898	CCACCTGGTACAGAG[A/C]AGGGTAGGAATACTT	54813
rs532292559	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963123	ACTTAGAGCTTCCAC[A/G]GCACTACTGCTTCCC	54813
rs532301266	snp	C/T	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44938659	ACAAGCGTGAGCCAC[C/T]GCGCCCGGCCGAAAA	54813
rs532334897	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939273	TAGTGTTCTGAGACT[A/T]CAACGGGAGGTACAG	54813
rs532339409	snp	C/T	8.24219e-05	0.00641905	missense	KLHL28	GRCh38.p7	14:44945817	CACCTACTCGAAGAA[C/T]GATGTCACAGAGTTC	54813
rs532368585	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940840	CTTATCTCTTTATTC[A/C]TCTAATTATAAAAAT	54813
rs532461704	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932714	GAAGAGTTGATGCAC[C/T]GCAGCAAGACTTTCA	54813
rs532480204	snp	C/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44929306	CATTTTAACAATCTA[C/T]TATTAATTATACAGG	54813
rs532499525	snp	G/T	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44932075	TCACCTAGGCTGGAG[G/T]GCAGTGACAAGATCA	54813
rs532725244	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955865	AAAAATATTCAGGGG[C/T]CAAACTAAATAGGCT	54813
rs532764935	snp	C/G	0.000461528	0.0151839	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963835	GGACCTCAGCAGGTG[C/G]TTTGTTTACTCCTGG	54813
rs532795424	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943294	TTAAACAATCAATTC[A/G]TGTAGCTAACATAAC	54813
rs532852720	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937439	GGCGTGATCCACTGT[A/G]CCCGGCCCAGAATTG	54813
rs532855149	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927157	GAAGAGACTAAAAAT[A/C]ACTTGCAAGGTTTTA	54813
rs532893823	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936718	AGCCATGGCCTAAGT[A/G]GAGAATTGAATTTAA	54813
rs532942196	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952219	AAAAATATGACTTTA[A/G]AAAAATGCACAGAAT	54813
rs533114766	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44951671	TTTATAATTGTATTA[A/G]ATGCAAATGATATAC	54813
rs533134080	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953226	TTAAATAAATGTGTT[A/G]AGATAACGGAATAGC	54813
rs533135589	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959893	TTTTAAGTCAATATA[C/T]GAGAAATTCCTAGAT	54813
rs533177425	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966885	GCTTGAGCCCAGGAG[C/T]TCCAGACTGCAGCAG	54813
rs533184654	snp	C/T	0.0193772	0.0965046	intron-variant	FAM179B	GRCh38.p7	14:44969178	CTTTCTTTTCTTTTT[C/T]TTTTTTTGTGAGACA	54813
rs533290671	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954153	TTGGTGAGGATGTGA[A/G]AAACAGGAAATCTCA	54813
rs533303658	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960697	GCCTCATTTACATTA[C/T]AGTCTATTCCCCACC	54813
rs533330220	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44969511	TGTCTTCTCATTCTC[C/T]TGACATTAACTTTCT	54813
rs533344097	in-del	-/T	0.00597247	0.0543191	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926639	AGCCTCCCAAGTAGC[-/T]GGGATTACAGGTACC	54813
rs533386297	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974639	ATACTGTTAAGGTGT[A/G]GGAGGTGGGGAAGTG	54813
rs533559986	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975209	GAAAACATCCAATAA[C/T]TACATTATACTGGAA	54813
rs533626089	snp	G/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44968540	GGCGTGAGCCACCGC[G/T]CCCGGCCTGGACTTT	54813
rs533705455	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44972135	ATCCCCCAGCAACCC[C/T]TCTTTCAACATTGAG	54813
rs533727808	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44970962	GTTGAGGATTTTCAC[A/G]TGTTTGTTCATAGGT	54813
rs533925519	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948529	TACCCCACTTATCTC[A/G]GAAGTTTACCTGAAA	54813
rs533936678	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44941876	AAATATTAATGTTTC[C/T]CAGATTTTCATTCAC	54813
rs534079640	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44944722	GTGGTCTGACTCAAA[A/T]AAACATGTAAATGGT	54813
rs534095342	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925487	CTAAGGAATTGCTTA[C/T]GCATAAACTAGGTCT	54813
rs534130687	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978844	AAGAAGAAGATCAAG[A/G]GCCAGGCATGGTGGC	54813
rs534172498	snp	A/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44965786	CCCTAAGAATACCCC[A/G]ACAACTTTTCACCCA	54813
rs534223902	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44972338	GAATTTAAGAAGAAT[A/G]TGCAGTCTGTTGTTG	54813
rs534238584	snp	C/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44958265	GAGTTTTGTACCTAT[C/G]TACTTAATTGACACC	54813
rs534325416	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44977213	AGCCTTAGCATAAAT[C/T]GAAGAAAATTAGACA	54813
rs534398473	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931671	CAAGAGTAGTCTGCC[A/C]CAAATGCTTAGGTTT	54813
rs534416217	snp	C/T	6.65779e-05	0.00576927	synonymous-codon	KLHL28	GRCh38.p7	14:44945911	AGCAAGCATGTAGGT[C/T]GGGGATGTGTGGTCC	54813
rs534440683	in-del	-/C	3.30218e-05	0.00406323	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963306	CAGGTTTCAATCTTA[-/C]ATTTCTCGTCTGCCC	54813
rs534547117	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44979554	GGGACACTTATTCAG[A/G]CTATTGCAGCAGCTA	54813
rs534602131	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928442	AAATTTATTACATCC[A/G]TAGCCCTAAAACCAT	54813
rs534630793	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968320	GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC	54813
rs534664594	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961947	AAACCCTAACTCTTA[C/G]GGGTGGGGCGGGCAA	54813
rs534682926	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44940475	AAAAATGCTTTCAAT[A/G]TATTGCCATCCTTAT	54813
rs534698995	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44938918	ATTCCCATGACTCCC[C/T]TAGCCATTGCCCTAG	54813
rs534812415	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936177	GGGTATAACTTTCCA[A/G]TGATTTTTACTATAA	54813
rs534828421	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44980254	CCACATGTAGGATTG[G/T]TTAGTGACATTAAAT	54813
rs534879691	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974714	GTTGGCATAAAATAT[A/C]TTAGCATTTTAAAAA	54813
rs534915736	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942284	ATTCAAACACCAAAT[C/T]CTGTCAATTTACTCT	54813
rs535045191	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44946150	ATTAGGAAATGGAAG[C/T]CCAAAAGGTTACATG	54813
rs535070656	snp	A/C	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44933523	TAAAGGTTCAGAATT[A/C]CGATTAATTTCTCAT	54813
rs535107158	snp	C/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925910	ATAGAAGGCAAGTAT[C/G]TTGCAACTGATTACA	54813
rs535117084	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44955848	ACTACAAGAGTCATA[C/T]AAAAAATATTCAGGG	54813
rs535119057	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44976529	TAATCTTAGTATCCA[A/G]TATCTTTAGCACAGT	54813
rs535233243	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953397	TTTAGTCCCCAATGC[A/G]GTAGTATTGAGAGGT	54813
rs535249583	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962296	GGCGGCCTGGCGGCA[A/G]GCTGAAGCTGTTCTT	54813
rs535305822	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957276	TCATCATATTGTTCT[A/G]CTTTTACATGTTTTT	54813
rs535387159	snp	A/C	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44939514	TTCTTCCCTCTCGCA[A/C]CTTACTATATGCAGT	54813
rs535575014	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44954634	AACATACATAATCAT[A/T]TCTATTAAAAAAAGG	54813
rs535608476	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44947852	CTGCAAATAATCTCA[C/T]ACCTATCTACTAGAA	54813
rs535617433	snp	C/T	0.00358779	0.0422022	intron-variant	KLHL28	GRCh38.p7	14:44952449	CTTAGGCAAAAGTTC[C/T]AGAACCAGTTAAAAT	54813
rs535656370	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44965654	TCAGGCTGTCCCATC[A/T]CTGGTGATGCTTAAT	54813
rs535680808	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44973285	GTTTCCCTAGAGTGT[A/G]TAATACACATTTACA	54813
rs535730181	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959659	AATTAACATATGTAG[C/T]ACACACATTCCTATA	54813
rs535761207	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44974377	TAGAAGTAACGCTTC[A/G]TGACTTATATTATCC	54813
rs535860716	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44960130	GCAATCTGTAATGTA[C/T]AGTGATCCACAGGGA	54813
rs535992844	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943714	ATAAAATGTATTATC[G/T]GACTTTTTTTTTTTT	54813
rs536013733	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44951710	CTTGTAAGAACTACT[A/G]AGAATAAAGTTTAAT	54813
rs536030463	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44977358	TCCTGCCTCAGCCTC[C/T]CTAGTACCTGGGACT	54813
rs536030902	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969625	AAAGTCATCACCATA[C/G]CCAAGGTCATCTAGG	54813
rs536073158	snp	A/G	0.0023933	0.0345097	intron-variant	FAM179B	GRCh38.p7	14:44976252	CCTTATTCGTTGCCT[A/G]TCTACATTTAACCTA	54813
rs536154011	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44933117	TATGCAAATAGCTGT[C/T]ATACTGTATTATTTT	54813
rs536501747	snp	G/T	1.87447e-05	0.00306137	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962427	ACAACCCTGCATGGC[G/T]GCTGCCCCCTCCGCG	54813
rs536534893	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44948610	AGAATATAGTACTTA[C/T]GTCTCACTGTACTAA	54813
rs536639593	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971763	CATTTATTTCAAAAT[A/G]TTTAAAAATTTCACT	54813
rs536733150	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44979375	CAGCACCTTCTTGCT[A/G]TGTCCTTATGGGGTG	54813
rs536740684	in-del	-/TTTG			intron-variant	FAM179B	GRCh38.p7	14:44967184	AAGGAGTACTTGTTT[-/TTTG]TTTGTTTGTTTTTTA	54813
rs536772523	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44944935	AAAGAAAAGTAAAAA[C/G]GAAAATCAAACTATT	54813
rs536774459	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44933368	CAGGCTGGAGTGTAG[A/T]AGTGCATTCAAGGCT	54813
rs536780314	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44970515	TTTTATTTCTTCCCA[A/G]TCTGTATACTTTTTA	54813
rs536814672	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940412	TGTTGAGATGAGTGA[C/T]GTGGCTGAATGTCCA	54813
rs536818394	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44934880	ACTCTTCTGAATGTC[C/T]ATTATAATTTTGCAT	54813
rs536829490	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44930837	GTTTGAGTTCAAAGA[C/T]AACAATTTTTCCTAA	54813
rs536952113	snp	G/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44932311	TTCATGTGGCTTACT[G/T]CAAAGCAATCACTGT	54813
rs537017696	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924116	CTCAGGTGATCTGCC[C/T]GCCTCAGCCTCCAAA	54813
rs537038934	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974687	TACACTTTTGATGAG[C/T]GTAATTTTATGGTTG	54813
rs537075795	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974060	TTAGGTTTCTGACAT[A/T]AATTGGGGGAAATTC	54813
rs537106771	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968245	ACATGCATATTTTAA[A/G]TTATTAGACTTTATT	54813
rs537114834	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975593	CACCTCAGCCTCCCG[A/G]ATAACTGGGATTACA	54813
rs537147667	snp	A/C	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44929605	ACTATCTGCAGTTTC[A/C]GTCCACTGGGGGTCT	54813
rs537184733	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44938807	TGGGCTTAGCCCATA[C/T]AGCTCTCACTGGTTG	54813
rs537220170	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943528	TGGGCATGATGGCAC[A/G]TGCCTGTAATCTCAG	54813
rs537230822	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952734	AAATTATACATGGCA[A/G]CTGTGACTATATTTG	54813
rs537393127	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953347	GTAATTATATAAATA[C/T]TAGAATAAAATACGG	54813
rs537404888	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947020	AATAATGGCTCCCCA[A/T]ATGACATTCACATCC	54813
rs537412748	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44941124	AGATGCCGTCTCCAA[A/G]TAAACAAAAAAAAAC	54813
rs537518013	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44974137	TCTTCCTAGTAATCC[C/T]ATTATACATATGTTA	54813
rs537547465	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926876	TTAAAAATAGTATAA[C/T]AGGATATATTTAATA	54813
rs537574301	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942771	ACATGAAGTTCTCTA[C/T]AATTCCTCTTCCCTA	54813
rs537575082	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932461	ATCCAAATTAAATCA[G/T]AATTTTCAAAAAGGC	54813
rs537579968	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978891	GTAGTCTCAGCTCCT[C/T]AGGAGGCTGAGACAG	54813
rs537580598	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44942700	CTTTGTACATTCCTC[A/G]TGACCTTTCTTCTTT	54813
rs537798300	snp	A/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44957252	GATGCGTGATAGGTA[A/T]ATAGATGTTCATCAT	54813
rs537966085	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44971795	GAGATTTCTTTGACT[C/T]GTATGTAACTTAGAA	54813
rs537978805	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941778	TCACATTCCTTCCTT[C/T]TTGACACACAAATTC	54813
rs538016961	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44980131	ATATTCATGTGTCCT[C/T]CATACTCAGTTACAG	54813
rs538017192	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44958893	TTTGGAAGATAAACC[G/T]AAGTAGATGAAAATA	54813
rs538029833	snp	A/T	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44964952	TTCCACTAGAAAAGT[A/T]AAAAAAAAAAAAAAA	54813
rs538128970	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44977028	ATACAATTATGTTAA[A/G]TTGTTTTATTTTTAG	54813
rs538261031	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958440	AAAAAGAGAAAATAA[G/T]AAATGATTTATCAAA	54813
rs538280182	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969412	CCACCTTGGCCTCCT[A/G]AAGTGCTGGGATTAC	54813
rs538387292	snp	C/T	0.00398564	0.0444627	intron-variant	KLHL28	GRCh38.p7	14:44951015	TTAGATAGTTTATTA[C/T]TTACAGATTGAAAAG	54813
rs538397932	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924190	TAAGACATGTTTTCA[C/T]TGTAACCTGCTAATG	54813
rs538471664	in-del	-/A	0.0023933	0.0345097	intron-variant	FAM179B	GRCh38.p7	14:44968141	TGTAATTACTTGTTC[-/A]AAAAAGGTCTTAGAA	54813
rs538615623	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44976602	TTAAAGTTATCTCAA[G/T]TGTAGATCATTTATT	54813
rs538663274	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962046	AGCTGCGTTTACAAC[G/T]TTCTGACTTCCTCTT	54813
rs538774896	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44952057	GTAGAGAAGGAGTTT[A/C]ACCATGTTGCCTAGG	54813
rs538805044	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928664	AGAAAATCATGGTTA[C/T]CAGGGAAGGAGAGCT	54813
rs538828070	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947036	ATGACATTCACATCC[C/T]TATCCCTGGAATCTG	54813
rs538841685	snp	A/T	0.00279162	0.0372561	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927597	ACTAAAACATGCTAA[A/T]ATCAAATAAGTTAAA	54813
rs538921961	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44979980	CACTGAGCCTCAGAG[C/G]AAAGTATATTAGTGT	54813
rs538996285	snp	G/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44939499	CCATTTTTAAATCAT[G/T]TCTTCCCTCTCGCAC	54813
rs539000738	snp	G/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44977331	GCTCCACCTTCCGGG[G/T]TCACGCCATTCTCCT	54813
rs539013380	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925295	AATAAACACAACATG[G/T]ACATATATTTCTCTC	54813
rs539020118	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970466	CTTTGAGACTTTCTA[G/T]GCAGACAATCATGTC	54813
rs539037606	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977789	TAGCTGGGACTACAG[A/G]CGTGTGCCACCATGC	54813
rs539061565	snp	A/C	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44973375	CCTTATAATAACAGA[A/C]TATTTGTAATTTCTT	54813
rs539134284	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44973989	AAGATGATATGCCTA[C/G]GTGTAGTTTTTCTGA	54813
rs539136085	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44936557	GGATGTTTTTAAGAG[A/G]GCAGAAGGTGTCAGA	54813
rs539175086	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926260	CTTCTAAATTTTGAA[C/G]ATTTTTCCTCTTCCT	54813
rs539194451	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939104	CTTACTACTTGTGCC[C/T]TCTAGAGTAGCAGCC	54813
rs539230118	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946235	CCAACTTTTTCATTT[C/T]GTTTCCCCTGCATTA	54813
rs539235483	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941974	CTCCATCAAAGACTT[A/C]ATAGTTTTAATTCAT	54813
rs539244155	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44955294	TACATATTAAATATA[C/T]GTAATATTATTTTAA	54813
rs539372878	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44968298	GGAGTTTCACTCTGT[C/T]GCCCAGGCTGGAGTG	54813
rs539482062	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44973852	TCTTCTTCTTTGTAT[A/G]GTTTCTGAGAAGTTA	54813
rs539597079	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950859	ATATCCATGAAATGC[C/T]TTTCCATGCATACCA	54813
rs539659790	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959273	AAAATGTTCCATAGT[C/G]CAAATGTAGAAGATG	54813
rs539763437	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942623	GGTTAGAACCCTTTA[C/G]TTCTGAATACCAATT	54813
rs539791316	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961085	GTGTCCGTTTAAGTA[C/T]CACTTATGAGGAGAA	54813
rs539835410	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952665	CAGCCTCATCAGTAG[C/T]TGGGACTACAGGTGT	54813
rs539971787	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44951647	TCATAAAAGAAAGCC[G/T]AGCATATTTTTATAA	54813
rs539979811	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44977482	ACCTCATGATCTGCC[C/T]GCCTTGGCCACCCAA	54813
rs540114538	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924587	ACATTCTTTGCAAGA[A/G]AGTACAAATATTAGT	54813
rs540164696	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927302	AACTGTAAATTGCCC[A/G]GCTATAGTATTCAAG	54813
rs540194704	in-del	-/CC	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44972131	GTCATCCCCCAGCAA[-/CC]CCCCTCTTTCAACAT	54813
rs540214072	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44930118	TCTCATTGTTTCTGT[C/G]GCTTTCCCTCTCAAG	54813
rs540240453	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947291	AGCTAGAAGAGCCAA[G/T]AACAGATTCTCCCGT	54813
rs540290708	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44956585	ATTAGCAAAAACATA[C/G]CGACTGTGAAAAATC	54813
rs540356561	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44974760	CCTTTACCCCTTTCG[A/G]TGTGTGTGTCTGGAA	54813
rs540369912	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931017	TGTATGTATGTAACA[G/T]ATGAAAAGATGACAT	54813
rs540391913	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927142	TTGAGTTCTAAATTA[A/G]AAGAGACTAAAAATC	54813
rs540448878	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953954	GCATATATAAAATAT[A/G]TATCAGTAATACATA	54813
rs540540904	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44968566	ACTTTAATTTTTAAA[A/G]CAGTTTTAGGTTCTC	54813
rs540621102	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957364	ATTTTGAATAAGACA[G/T]TTTTAGAATCCTAAG	54813
rs540658808	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961242	CAATCTCTGTCTCTA[A/G]GAGACTGAAAGGCTG	54813
rs540674891	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44949136	TGAGATTATTGAATC[A/G]TTACCAGTGCCACAG	54813
rs540716210	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44954491	TATAGAGCATCCACA[C/T]AATGCAGTACTATAC	54813
rs540716707	snp	A/G			intron-variant, synonymous-codon	KLHL28	GRCh38.p7	14:44937785	GGTCATCTCATGGTA[A/G]AAGACATCACATGGA	54813
rs540719288	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952846	GTCAAACAGTTTTAC[A/T]CTGGCAGTTTCATTT	54813
rs540752932	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44940319	AATTTTGGAGGGACA[-/C]ATTTAAACTATAGCA	54813
rs540820951	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971292	TTTTACACATTGTGT[C/G]TTTCAAGGAATTGAT	54813
rs540865331	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970679	CTGTATGCTTTCTTG[C/T]AGTGTTCGCTATAAA	54813
rs540889995	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44964566	TTGAGGGAAACATGT[C/T]ATGCTTTGTTTTAAA	54813
rs540933667	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44959857	TGTACTCTCTCTATA[C/T]ATGATTAAATACAAA	54813
rs541009151	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952190	ATTTTTAATTTGGCC[C/T]CTTTCCTCTCTCAAA	54813
rs541045943	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960572	TCCCTAAAATGAAAC[A/G]TGCTAGCTAAACCTA	54813
rs541068759	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928877	CAAAACTACTTCTCA[A/G]TTAAAAGTACCCAAC	54813
rs541089638	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969736	TATGAAGGGTGTCAG[A/G]TCTGTTTCTAGATTC	54813
rs541105277	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44975669	ACAGGGTTTCACCAT[A/G]TTGGCCAGTCTGGTC	54813
rs541128477	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969132	CCTTCCTTCCTTCCT[A/T]CCTTCCTTCCTTCCT	54813
rs541149254	in-del	-/TT			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925594	CTATATTTTACTCTC[-/TT]TGAGTGAAAAAGAGT	54813
rs541205932	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937426	TGCTGGGATTACAGG[A/C]GTGATCCACTGTGCC	54813
rs541219971	snp	C/G	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44974102	TGCCTCAAATATTTC[C/G]TCTATTCTTTTCTAT	54813
rs541224461	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925749	ACTTCCTATAATTTA[A/G]TATTCACTCACATTT	54813
rs541244122	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944656	CACAGGTTCCTAGTT[C/T]TCTTCTTTGCTATCT	54813
rs541297708	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967413	AACTACCTACTAAGT[A/G]AAGTTTAAGATTTCG	54813
rs541349131	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44949229	TTTCAGATAACATTC[C/T]AAAACAAATTATTAA	54813
rs541363628	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44938167	AGTCTATCTAAATCA[C/T]ATATAAGCGAGAGTC	54813
rs541463846	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44971654	ATGATCGATTTTAGA[C/T]CTTTCTTCTTTTCTA	54813
rs541488466	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44965344	TGTTTTATATTTCTT[C/G]TTTTACTTTTATCAT	54813
rs541499024	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44977446	TTTCACCGTGTTAGC[C/T]GGGATGGTCTTGATC	54813
rs541537263	snp	C/T			intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937502	TGGAAAATTGGTTGG[C/T]ATGAGAGTAAGACTT	54813
rs541600929	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940678	CAGCCAGTAAACCTC[A/T]ATTGTCTTGAGGCAT	54813
rs541744827	snp	A/T	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44978211	ACCTCATTGGAGCAA[A/T]ATACGAGGTATAGTT	54813
rs541761206	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941272	CATTCAGTTTATTTC[C/T]TTACTTTGTATTCAC	54813
rs541799335	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931899	TGAATAAGTCATTTC[C/T]TCTCACCTGCAAAAA	54813
rs541958092	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44952869	TTTCATTTACCTCAG[C/T]AACCACTTTGCGTAA	54813
rs542051822	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44968557	CCGGCCTGGACTTTA[A/G]TTTTTAAAGCAGTTT	54813
rs542186296	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44947771	TTCACAATGAATTTT[A/C]AGTCAGTTAATAAAT	54813
rs542402313	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958578	AGCCTATGGAATAAG[G/T]TAGGATATTTTCCTT	54813
rs542430100	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44949366	AAAATTTATTTAGAA[G/T]ACTTGTAGATCAGAA	54813
rs542465644	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950446	CTATATTGTTAACCT[A/G]ATTTTTGTGTACCCA	54813
rs542584879	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44938517	GCTGGGACTACAGGC[A/G]CCCACCACCACGCCC	54813
rs542611970	snp	C/T	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44977437	AAGACGGGGTTTCAC[C/T]GTGTTAGCTGGGATG	54813
rs542622733	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946466	ATTACCACCAATTAA[C/T]TTAATTAATTATGAA	54813
rs542648627	snp	A/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44955738	CTGCAGTGTGCAGTG[A/T]TTGCACAACTGCACT	54813
rs542663890	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947386	TTCTGGCCTCCAAAA[C/T]TGTGAGAGAATACAT	54813
rs542685317	snp	A/G	0.000445548	0.014919	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963769	GCGGACAACAAGTTG[A/G]TGATCAAACAAGAAT	54813
rs542747094	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942213	TAATCATCTAATCAA[A/G]AGAACTCATTCATCT	54813
rs542963038	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44940614	TAAAGAAAAAAACTA[A/C]AGCCATTGGACAAGT	54813
rs542968447	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44948701	TACTCTTATGATGCT[A/C]ATGTAATGACTATAG	54813
rs543006198	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926082	TTTAACATAGAAACA[C/T]GTGGCTTTAAATTCA	54813
rs543185284	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924671	TTATAATACACAGCA[A/C]AATTCATAAGGCAAA	54813
rs543272768	snp	A/G	1.65842e-05	0.00287955	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962608	GGTTCCTGCCCCACT[A/G]CAACTTCGCCTCTGG	54813
rs543284089	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44976984	AATTTTGCTCAAAAT[C/T]GCTAACGATTAAAAG	54813
rs543310527	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970619	CCTTGCCTTGTTTCT[A/T]ATCTTAGTGGGAAAG	54813
rs543398265	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959801	ACTATTAATAAAACA[A/C]CTAATAGTGTATTCT	54813
rs543435204	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966640	TTTCATGATAAAATT[A/G]TCCCAAATTTAACTA	54813
rs543462349	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937269	TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGATT	54813
rs543495920	snp	A/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44929274	ATAAATTTGTATTTT[A/T]ATGTTTTATTAAAAT	54813
rs543515264	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975094	TATATTTTTTATATA[C/T]CAGAAAGCAATAATT	54813
rs543595428	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943944	TTGTCTCAAACTCCA[A/G]TCTCAAGTGATCCTC	54813
rs543608685	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44949787	ACGCATCTGTAGAAC[A/G]TGTTTAACAGGTTTA	54813
rs543614724	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44933920	GAATGTAAAATTTAA[C/T]GAGAGGGATTTGATT	54813
rs543630050	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952136	AAGTGTTGGGATTAC[A/T]GGTGTGAGCCACTGA	54813
rs543631813	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44943182	GGCAACTGCTCAAAA[A/T]TTTTTACACTATAAA	54813
rs543727451	in-del	-/TGA	0.00636936	0.0560724	intron-variant	KLHL28	GRCh38.p7	14:44944447	TTTATAGAAAAAGTC[-/TGA]TGACAATTCCTAATC	54813
rs543746721	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972774	TATATTTAAAATGGG[C/T]TTCTTGTAGACAGCC	54813
rs543761320	snp	A/C	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44977496	CCGCCTTGGCCACCC[A/C]AAGTGCTGGGATTAC	54813
rs543866962	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968421	CCCGCCACCATGCCC[A/G]GTATTTTTAGTAGAG	54813
rs543931894	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44959456	CAATAACTTCTCAAA[C/G]TACACAAAATTCTTA	54813
rs543941429	snp	G/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44971610	TTAATTTGCTCTTCC[G/T]TTGTTAGTTTCCTAG	54813
rs544020965	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955718	TTGTGCCCAGGAGGT[C/T]GAGGCTGCAGTGTGC	54813
rs544063411	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947307	AACAGATTCTCCCGT[A/G]GAGCTTATGGAAGGA	54813
rs544142881	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936567	AAGAGAGCAGAAGGT[A/G]TCAGACATGAGGGAG	54813
rs544196778	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931857	CTGAACGAACCTTAA[A/C]CCTACTGCTGTGGAT	54813
rs544201752	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940531	ATACAGTTCTCAGAG[C/T]TTCCCCAATTTTCTT	54813
rs544229635	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939835	CTAGGCTTCTTCCAG[A/G]CTCCTACTTAAAATT	54813
rs544347187	snp	C/G/T			intron-variant	KLHL28	GRCh38.p7	14:44937128	GTCAGAATTGAATTG[C/G/T]TTTTTTTGTTTGTTT	54813
rs544393993	snp	A/C			missense	KLHL28	GRCh38.p7	14:44934515	GAATGTTTAGGGGTG[A/C]CAAACCAATCCAAGA	54813
rs544495884	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44951920	GGTGTGGTGGCGAGA[C/T]CTTAGCTTACTCACT	54813
rs544538524	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44956381	GTTTATATCACAAAA[A/G]GAGAGATAGCTAGAT	54813
rs544599712	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950330	TTCTCTGATACCCTG[C/G]GCAACACAAGTATCA	54813
rs544631358	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44949773	ATAAGAGAGAAAAGA[C/T]GCATCTGTAGAACGT	54813
rs544638405	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44949265	TGACTTGTGAATACC[A/G]ATAAGAAGATGTAGA	54813
rs544684169	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44931210	ACCACATACAAGTCT[-/T]TTTTTTTTTTTTTTC	54813
rs544693959	in-del	-/TTCTTTTC			intron-variant	FAM179B	GRCh38.p7	14:44969173	TTTTCTTTCTTTTCT[-/TTCTTTTC]TTTTTTTTTTTTGTG	54813
rs544740334	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942004	TACCTCTAAACTATA[C/T]TATATGCTGATGACC	54813
rs544785877	snp	C/G	0	0	intron-variant	FAM179B	GRCh38.p7	14:44965260	TTATTGCACCTAAGA[C/G]TATCAGTAGTAATTC	54813
rs544822316	snp	C/G	1.64912e-05	0.00287147	missense	KLHL28	GRCh38.p7	14:44945538	TACCAGGATCAAGTT[C/G]GCTTTCAAGAAATGC	54813
rs544873871	snp	A/G	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44968389	CTCAGCCTTCCGAGT[A/G]GCTGGGACTACAGGC	54813
rs544909443	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974936	AAATAGGTCTTTAGT[A/C]ATGTACAATTAAGGT	54813
rs544955153	snp	C/T	4.94507e-05	0.00497221	missense	KLHL28	GRCh38.p7	14:44945449	TTCAAAATTCTGGCA[C/T]ATGTATTTAGTGGCT	54813
rs544971215	snp	C/G	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44944718	TGATGTGGTCTGACT[C/G]AAATAAACATGTAAA	54813
rs544996265	snp	C/G	5.10669e-05	0.0050528	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962504	AGAGCCGCAGTCGTC[C/G]TTCCGCCCCAGAGAC	54813
rs545003849	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925265	CAATACCAGGAATCC[A/C]ACACCAAAACTGAAA	54813
rs545007033	snp	A/C	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	KLHL28	GRCh38.p7	14:44953706	GACTTCTCAGCCTCC[A/C]TAACTGTAAGAAATA	54813
rs545057285	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954883	AATATCAACTTAGTG[G/T]CCTTACCATACCATT	54813
rs545084900	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44970556	TGTCTTATTGCATTA[C/G]TTTGAACTTCCAATA	54813
rs545106659	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969767	ATTTTTTTTTACATG[G/T]GCATGTTCAGTTGTT	54813
rs545133739	snp	C/T	0.00398564	0.0444627	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937442	GTGATCCACTGTGCC[C/T]GGCCCAGAATTGAAT	54813
rs545138846	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44954256	TTTGGATTTTTCCTT[C/T]GACCCAAAAACCCTA	54813
rs545218725	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960722	CCCACCCCCACCCCC[C/G]CAAAAACAAAACAAA	54813
rs545221669	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967495	AAACTTTTCTTAAAT[A/T]AAGTCTTTTATCTAT	54813
rs545234559	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44975781	TTCCCCTGCCTTTTT[C/T]TTTTTTTTTAATGAA	54813
rs545273083	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977516	GCTGGGATTACAGGC[A/G]TGAGCCACAGCACCC	54813
rs545355333	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44933733	TGTGCTATAATATTG[C/T]ATAGACACACAGGAA	54813
rs545454614	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958729	CCATGTTATGACAGG[A/C]GTCTAAGTTACATAA	54813
rs545454769	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44966597	AATAATTACATATTA[C/T]TTTTTGTTACTAAAT	54813
rs545652906	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969214	GGCTGGAGTGCAGTG[C/T]GATCTCGGCTCACTG	54813
rs545691786	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975796	TTTTTTTTTTAATGA[A/T]GTGGGTTTGAACCAT	54813
rs545717189	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44929916	CAGGAAAATGGAGTA[C/T]ATATCTTTCCATAGG	54813
rs545751471	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972094	ATGAGAACAGGAAAG[A/G]GGATATCCAACCCCA	54813
rs545886637	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44943850	CTCCTGATTAGCTGG[A/G]ACTACAGGAGTGCAA	54813
rs545995670	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941315	TGTAATGTATCTACA[A/G]CATTTCTACAACTCT	54813
rs546103820	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950623	GACTGGGCTTTGGTA[C/G]CAGGCTTCCCGGGTT	54813
rs546188458	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925832	AAGCCACTTACATTC[C/T]ATTACAACATCCAAT	54813
rs546190491	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936320	TGGTAATGATACATA[C/T]AGTACAGAGGGAGAA	54813
rs546363340	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44951301	CCTTAGAGGCCTCTC[A/C]CTCTCTCATATTCCA	54813
rs546376344	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44943161	TTAATAGTTGAGAAA[A/G]TAAGAGGCAACTGCT	54813
rs546499607	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944942	AGTAAAAAGGAAAAT[A/C]AAACTATTTTTAAAA	54813
rs546691195	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970014	TCCATGTTGAGTTCA[C/T]TCTTCTGGGTTTTTT	54813
rs546693188	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962328	TGCCTCTTCTGCAGC[C/T]TGGGGCTTGGAGAGG	54813
rs546727929	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44969358	GGATTTCACCATGTT[A/G]GCCAGGCTGGTCTTG	54813
rs546857039	snp	C/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44975314	CAAGTTTTATTTTCT[C/G]TTAGAGGGAATAGCT	54813
rs546935178	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946972	ATGAGAAAGAAAAGA[A/G]AGTGGAGAGACAATA	54813
rs546980465	snp	C/T	0.000115391	0.00759487	missense	KLHL28	GRCh38.p7	14:44934427	ATAGTGACGCCAGGA[C/T]GCACATTAGTTGCAA	54813
rs547019700	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44957667	AATTCCTTTCATCCT[A/C]AGAGCAACAATATAA	54813
rs547042556	snp	G/T	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44935311	GAGGACAAGAAGGGA[G/T]CTCAAGGGTGGCTTT	54813
rs547104546	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44951636	TAAAAGTAACTTCAT[A/C]AAAGAAAGCCTAGCA	54813
rs547159815	in-del	-/G	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44932257	AGAGGGGTGGGGGGT[-/G]GGGGAGAAAAACCTT	54813
rs547285785	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44966116	CTGACCCACCCGCCT[C/T]GGCATCCCAAAGTGC	54813
rs547385341	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961518	TAACCCTCTGCGGCC[C/G]GAGGGTTAAGAGAAG	54813
rs547603708	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936690	CTCCAGTTACATTCT[A/G]CTGCTCAGATGTAGC	54813
rs547633028	snp	G/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44973796	TTCTAAATTGATGGG[G/T]TTTTTTTTTCTCTCA	54813
rs547635963	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950816	TTTACTGTTCATCAA[C/T]CTTTAAAAAGCTTGG	54813
rs547650512	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966117	TGACCCACCCGCCTC[A/G]GCATCCCAAAGTGCT	54813
rs547671808	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959239	CTCTGTCCAATTACT[C/G]TTTTGTGGAAACACC	54813
rs547697687	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967131	TGCTCATTGCTATTT[C/G]TTGCCATTGTGGTTT	54813
rs547788757	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925625	TATATCTCTCTAGCT[C/T]CCACAGCATCTAACA	54813
rs547870605	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944377	AATGGCAGAGTTAAG[C/T]AGATGCCACAAAGAT	54813
rs547988608	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926231	GTAGGTTAAGCAATC[A/C]TAAAATAAATATACT	54813
rs548056339	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970825	TTAAACCTGATGATG[C/T]GATGGGTTATATTAA	54813
rs548066487	snp	A/G	0.00358779	0.0422022	intron-variant	FAM179B	GRCh38.p7	14:44977528	GGCGTGAGCCACAGC[A/G]CCCGGCCAAGACTGA	54813
rs548085942	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44970961	TGTTGAGGATTTTCA[C/T]ATGTTTGTTCATAGG	54813
rs548231046	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44956940	CTCCCTCCTCAGCCT[A/C]CCAAGTAGCTAGAAC	54813
rs548293359	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926804	TGAGCCACTGCGCCC[A/G]TCCTAAAATCATTTT	54813
rs548336469	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44956041	ACTCATTTTTTGAAA[C/G]CTAGTAAACAAAGAG	54813
rs548542928	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924056	TGTATTTTTAGTAGA[A/G]ACGGGGTTTCAGCAT	54813
rs548555695	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932324	CTGCAAAGCAATCAC[A/T]GTAGATTGCATAGTA	54813
rs548582272	snp	A/C/G	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44932782	CAAATTTTGGGCAGA[A/C/G]GCTTTTCAAAGAATA	54813
rs548643976	snp	G/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961191	CTCTTAGAACCATGA[G/T]GCCAAGAACTTCCAC	54813
rs548675150	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44965765	CAGTACAGTGATACT[G/T]TGAGACCCTAAGAAT	54813
rs548676975	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972873	TACAGTAAGTCCTCA[A/C]ATAACGTTATTTTGT	54813
rs548713203	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972289	GTTTTTTTTTTGCGA[A/T]AGAACGTGGTATTTC	54813
rs548783829	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44943794	TTCATAGCTCACTGC[A/G]ACTTCAAACTCCTGG	54813
rs548792960	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44941018	GGCAGGAGAATCGCT[C/T]GAACTCAGGAGGCAG	54813
rs548954291	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44946851	ATGGGCCACCACACC[C/T]GGCCTCAACTCTTGA	54813
rs548979318	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927289	TGGAAGAACAAAGAA[C/T]TGTAAATTGCCCGGC	54813
rs549002160	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44941569	GGAGGCGGAGATTGC[A/G]GTGAGCCGAGATTGC	54813
rs549017814	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939367	CCTGTAACCACACTC[A/T]TCTCTTTAGCACACA	54813
rs549039998	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44978840	AAAGAAGAAGAAGAT[C/T]AAGAGCCAGGCATGG	54813
rs549046307	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958211	TCTACAGTAACTTAA[C/T]TTTAGGCTCTGAAAC	54813
rs549076759	snp	C/T	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44975844	CTCAAAACAACACAG[C/T]TTTGGTATTAGGACA	54813
rs549207720	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44954636	CATACATAATCATTT[A/C]TATTAAAAAAAGGAA	54813
rs549229686	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952403	GGTTGCAGGAAATGG[C/G]CAAACTGTGTTTTAA	54813
rs549250425	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944819	AAGTGTGCACTTGGG[A/G]AGATGGTTAATAATT	54813
rs549374202	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954467	CAACAAAAGAATGGT[C/T]GTGAAAACTATAGAG	54813
rs549388938	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44954980	CTGTTTTCAGTAATC[A/G]CATTGTTGATAAGGA	54813
rs549412970	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962280	GCCTCCCGGAGTTGG[A/G]GGCGGCCTGGCGGCA	54813
rs549431081	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44938521	GGACTACAGGCGCCC[A/G]CCACCACGCCCAGCT	54813
rs549447060	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939462	AAGTCTTTCTGTTCC[A/G]CTTACCATTTAATTA	54813
rs549578697	snp	A/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44965071	TCTATAGGTAAGAGT[A/G]CAATGAATACCCATA	54813
rs549591304	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961868	TCAGTAATCACACGG[A/G]CAGCGACAGGAGGAG	54813
rs549637694	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969313	CACACCATCATGCCC[A/G]GCTAATTTTTTGTAT	54813
rs549750232	snp	C/T	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44964989	GGAAAAAGAAAAAGC[C/T]TCCACAGAAGATACA	54813
rs549801542	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942358	CTACTTCTACCCTAA[C/T]TTAGGATCTCATCAT	54813
rs549953900	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44932068	CGCTCTGTCACCTAG[G/T]CTGGAGTGCAGTGAC	54813
rs549992161	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972237	GAGCAAATATTGTAT[C/G]ATTTCTATTCTTTTA	54813
rs550009811	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967675	TTTTGCACAGCAAAC[A/G]CAAGGGGCCTAGTGG	54813
rs550027467	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44954931	AGTAATCTGAAGTCT[C/T]TATTGCGACATGCCC	54813
rs550056034	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44965562	TTAGGAAAATATTAC[A/G]TAGGAGATACATATA	54813
rs550093841	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44935225	GTCAAATTCAAAAGG[A/G]TATCAATTAAGTTCA	54813
rs550185979	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44930282	ATGAAATCCAAAGTG[C/T]TCCAACATTTGAAAC	54813
rs550191056	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967099	GGTATTTGAAAACAA[A/G]AGTCTGAGTATAGAT	54813
rs550235717	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44970557	GTCTTATTGCATTAG[A/T]TTGAACTTCCAATAT	54813
rs550267117	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44951915	GCCAGGGTGTGGTGG[C/T]GAGATCTTAGCTTAC	54813
rs550347094	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970071	GTTTGTTGATGTCCA[A/G]AAAATAAGTTGCTGA	54813
rs550466732	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44933943	ATTTGATTGTTAGGT[C/T]TGTATTAAATTCCCA	54813
rs550543821	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925944	ATTTCTATTTCCCAG[C/T]GCTGCTCTTTTCCAA	54813
rs550658054	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970716	AAAGTTCCCCCTGTA[C/T]TCCTAGTTTGCTGAG	54813
rs550779006	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44929329	TATACAGGCAATATA[C/T]AGTAGTCCTCCCTTT	54813
rs550876604	snp	A/G			intron-variant, utr-variant-5-prime	KLHL28	GRCh38.p7	14:44953684	AGGTGTGGCCCCCTT[A/G]ACCTTGGACTTCTCA	54813
rs550912660	in-del	-/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937642	GGTCTTTTGATGGTG[-/T]CTTAGTTCATTTTCT	54813
rs550941760	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44930224	TTGTTTCAAAAGGTT[A/C]TTTAATCATAAATAT	54813
rs550976831	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940873	TTGGGAGGCTGAGGC[A/G]GGTGGATCACAAGGT	54813
rs551028267	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44931835	TACTAATTCTGTATA[A/C]CTAGGGCTGAACGAA	54813
rs551071752	snp	G/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44936719	GCCATGGCCTAAGTG[G/T]AGAATTGAATTTAAC	54813
rs551106803	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927166	AAAAATCACTTGCAA[A/G]GTTTTATAATCTGTG	54813
rs551108589	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944007	GGTATTTTGAGACTT[G/T]TTTAAAGATGCAGAA	54813
rs551115380	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44979288	TTATTGCTCCCAGTT[C/G]TGGGGACTGGGAAAT	54813
rs551127732	snp	C/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44977163	TTTATATATATGATT[C/G]ATTGACTAGAAATAA	54813
rs551230257	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955875	AGGGGCCAAACTAAA[C/T]AGGCTTTCACTAGTC	54813
rs551254845	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948325	ACTGTAAGTGATATT[A/G]TACTACAGTAGTACT	54813
rs551295973	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961880	CGGGCAGCGACAGGA[C/G]GAGGAACCGCGGACA	54813
rs551445251	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44947034	AAATGACATTCACAT[A/C]CCTATCCCTGGAATC	54813
rs551463759	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44974984	TTCTGTAGTGCTTTA[A/G]TTACACTTTTGATGA	54813
rs551472283	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44969920	TATTTTTGCCCATAA[C/G]ACATTGTCTTGATTA	54813
rs551567585	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928064	CTGAACATCCAAAAG[A/G]ACATCAGTTATAGCC	54813
rs551629162	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961648	TCCTGATAAGCAGAT[G/T]GCAAGAGGAAAGGAT	54813
rs551659149	snp	A/C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952225	ATGACTTTAGAAAAA[A/C/T]GCACAGAATTCTAAC	54813
rs551669484	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44959333	ATGAGTTAATATTTA[C/T]TAAGTACCTAGCATG	54813
rs551712211	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44944228	AGTTACTAGTATAAT[C/G]CACCAAATTAAGGGT	54813
rs551732299	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44975216	TCCAATAACTACATT[A/G]TACTGGAATGAATGA	54813
rs551750193	snp	G/T	0.000153969	0.00877272	intron-variant	KLHL28	GRCh38.p7	14:44945025	TAGGAAAGCCTTCTA[G/T]TTACCTATCCAAACA	54813
rs551753911	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958003	CCATGGAACAATCAT[G/T]GCCTTCCAGTATTTG	54813
rs551758423	snp	A/G	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44940957	ATACAAAAATTAGCC[A/G]GGTGTGGTGGCATAT	54813
rs551763153	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44941166	TCTTCAAGAACAAAA[A/T]AAAACCAAACAAAAC	54813
rs551792539	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957139	GTATTGAAATATTTG[C/T]AGATGAAATAATATG	54813
rs551793668	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968622	TAGTTCCCATATACC[C/G]CTGTCCACACAAGAA	54813
rs551885191	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948603	GGTGTTAAGAATATA[A/G]TACTTACGTCTCACT	54813
rs551961626	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931971	TCAAATGAGTATGCA[C/T]GTGACTTTGAAAACC	54813
rs552002362	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44944910	AGAAGAAAAAAAACT[A/G]AAAAGAAGCAAAGAA	54813
rs552063685	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942005	ACCTCTAAACTATAC[C/T]ATATGCTGATGACCT	54813
rs552226717	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44952186	TAAAATTTTTAATTT[A/G]GCCCCTTTCCTCTCT	54813
rs552361307	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967075	AGTACTGCCTTTTTA[C/T]TGGGCAGTGGTATTT	54813
rs552398292	snp	A/C	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44973616	TATACATATATATAT[A/C]TCTCTCTCCAGGTTT	54813
rs552478255	snp	C/T	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44942233	CTCATTCATCTTGGA[C/T]TCCTCCCTCTTCCTC	54813
rs552544344	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44933891	TTTTAAAATCTAGTC[C/T]ATTTATAGTGAATGA	54813
rs552574627	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44979654	TCTCTTAGCTAGTGA[C/G]TGGCAGAGCTGATTT	54813
rs552672727	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959482	TCTTAATAGTTTACA[A/G]AATTCACACTGACGT	54813
rs552688288	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44970881	TTGCATACCTGGGAT[A/G]AATTCCACTTGGTTG	54813
rs552714230	in-del	-/G	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44955679	TAGTCTCAGCTACTT[-/G]GGGGGCTGAGCTAGG	54813
rs552767936	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953401	GTCCCCAATGCGGTA[A/G]TATTGAGAGGTAGGG	54813
rs552786832	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44933079	TTGTATACTTTAAAT[A/C]ATCTCTAGATTACTT	54813
rs552891373	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44938669	GCCACCGCGCCCGGC[C/T]GAAAACATTAAGTCT	54813
rs552956214	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44949116	TATTTAAAAGAGCCT[A/G]CAAATGAGATTATTG	54813
rs553033506	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962469	GCCGCCCTTTCCAGT[C/T]CTCTCTACCTATCGG	54813
rs553115855	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962011	TCAAATGGCTTCACC[C/G]CTCCTCCCTTCTCCG	54813
rs553135032	snp	C/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44977716	TGAGCTGCACTTGCA[C/G]CTCACTGCAACTTCC	54813
rs553145867	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44938170	CTATCTAAATCATAT[A/T]TAAGCGAGAGTCAAG	54813
rs553200508	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44968408	GGGACTACAGGCACC[C/T]GCCACCATGCCCAGT	54813
rs553209206	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928900	TACCCAACAAAACTT[C/T]TGAGCCTTCATGCTA	54813
rs553287573	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968323	GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC	54813
rs553330147	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44947688	TCATTCTTATACATT[A/T]TTAAGTGGAAAAAAT	54813
rs553411002	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977327	GCAAGCTCCACCTTC[C/T]GGGTTCACGCCATTC	54813
rs553436074	snp	C/T	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44965927	TTGCCCAGGCTGGAG[C/T]GCAATGGCGCAATCT	54813
rs553436162	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44973356	TTCACAGGTAACCCA[A/G]GTACCTTATAATAAC	54813
rs553527235	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946182	GATGCCCCAAACCAA[A/G]AAAATCTCTGACAAT	54813
rs553543314	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925090	TACAAAGGGAAAAAA[A/G]GTTAAGAAGTAGAAC	54813
rs553548168	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941285	TCCTTACTTTGTATT[C/T]ACTTCTAGGCCCACT	54813
rs553561786	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44935152	TGGCAATGAAAGGAA[A/C]AAACTATAGCTACAT	54813
rs553566511	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44954602	GTCACCATTTATCTA[C/T]GATAGGGAAGATTAC	54813
rs553599736	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958260	GTTGCGAGTTTTGTA[C/T]CTATCTACTTAATTG	54813
rs553616026	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941937	CACCAGGCAAAAGGA[A/G]GAACATTTAAACTGT	54813
rs553721252	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924394	AATTACAGAACATTA[C/T]CACAATGATACACAC	54813
rs553746775	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44968676	ACTTTAGGGGTACAT[C/T]TGTTATAATCAGTGA	54813
rs553785418	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950154	GTTTTGAGGATTAAA[C/T]GAGTTTATACATAAA	54813
rs553913441	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44951949	CTGCAGCCTTGACCT[C/T]CTGGGCTCAGGTGAT	54813
rs553967476	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44949029	CGAAAAATAAGAGAA[A/G]GGATTGAAAAAGGAG	54813
rs553975810	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44931310	TTGCCTTACATGTTT[A/C]GAAATTAATAAATTC	54813
rs554240229	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943043	GCTCTATGCAAATAA[C/T]ACTTTTAATTTTTAA	54813
rs554313782	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44941955	ACATTTAAACTGTCA[A/G]TAACTCCATCAAAGA	54813
rs554371552	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44966748	TGCTTGAGGCCAGGA[C/G]TTCGAGACCAGCCTG	54813
rs554419670	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44951238	TGACACACTTGTAGG[A/G]GAAATAGAGAGGTGA	54813
rs554460494	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959669	TGTAGCACACACATT[C/T]CTATAATTCACTAAT	54813
rs554545325	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954835	AAAACATGATCCATA[A/G]GAAATTTGAAAATTG	54813
rs554589123	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955638	AACAAATAAAAAAAT[C/T]AGCTGGATGTGGTGG	54813
rs554645673	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946499	GAATCCAAAGTCCCA[A/T]GAGGGCAATAAGGCT	54813
rs554671824	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939634	GTCTTTGCTAATATA[A/T]AGCAAGGATGGCCTT	54813
rs554708954	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947259	CCACAAACCAAGGAA[C/T]GCTGGCAGTCACCAG	54813
rs554775670	snp	A/G	0.00597247	0.0543191	intron-variant	KLHL28	GRCh38.p7	14:44956413	ATTGGGCCTTCTGAT[A/G]GAAAAACATAACACC	54813
rs554930952	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44949429	AATAATTTTATAATG[C/T]CCTTCATGATTTTTC	54813
rs555021010	snp	C/G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957303	TTTTGAAATTTTGCA[C/G/T]AGTAAGAGACTTTTT	54813
rs555135904	snp	C/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44931594	TTGTGTCATTCTTCC[C/T]GTCAAAGCAAAACTA	54813
rs555145578	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961195	TAGAACCATGATGCC[A/C]AGAACTTCCACCGCA	54813
rs555220055	snp	C/T	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44977914	CACTGCCTCTGAAAG[C/T]GCTGGGATTACAGGC	54813
rs555232472	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940469	TATTCAAAAAATGCT[G/T]TCAATGTATTGCCAT	54813
rs555248298	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44953263	GAAACAGGTAAAACT[A/C]GATTTCTGCTACATA	54813
rs555293580	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967392	GCTAGACCAGCAACA[A/G]CAACCAACTACCTAC	54813
rs555325335	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926575	GCAATGGTGCAAGCT[C/T]GGCTCACTGCAACCT	54813
rs555339257	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44974397	TTATATTATCCTTTT[C/G]TTCTTACATGTTGTC	54813
rs555454934	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960457	TGACTAGAAGTCTAC[A/G]CATTTGAGCTTCTTA	54813
rs555465333	snp	C/T	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44975634	ACCACTTCTGGCTAA[C/T]TTTTGTATTTTTAGT	54813
rs555468331	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928797	ATTCAATTGGCAAAG[C/T]CTTTACTTTTTTTTT	54813
rs555527959	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925614	GTGAAAAAGAGTATA[C/T]CTCTCTAGCTCCCAC	54813
rs555564582	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44971330	ATCTAGGTTACCCAA[C/T]TTATAAGCATAGAGT	54813
rs555579910	snp	C/G	0.0126979	0.078662	intron-variant	KLHL28	GRCh38.p7	14:44952758	ATATTTGGTTCTCAG[C/G]TATCTACCCATAAAT	54813
rs555689288	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974086	AATTCTCAGTAATTA[C/T]TGCCTCAAATATTTC	54813
rs555725259	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44933299	AAAGATACAATCTTT[A/T]CTTTTCTTTCTTTCT	54813
rs555786046	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44929626	CTGGGGGTCTTGGAA[C/T]ATATATCTCCTGTGG	54813
rs555830078	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971977	ATGGCAGAAAGTGAA[A/G]AGGAAGGAGTCACGT	54813
rs555994799	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937308	GCACCACCACCCTCA[A/G]CTAACTTTTTTTGTA	54813
rs555997230	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44948333	TGATATTGTACTACA[C/G]TAGTACTATGGTAGC	54813
rs556007616	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948853	TTAACTTTACCTGGA[C/T]GTCTATAAGCATTTA	54813
rs556044742	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947976	TACTAGTAAGTAGAT[A/G]GCAATCAGAAGGCAT	54813
rs556112043	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932462	TCCAAATTAAATCAG[A/T]ATTTTCAAAAAGGCT	54813
rs556125958	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44977448	TCACCGTGTTAGCTG[C/G]GATGGTCTTGATCTC	54813
rs556147939	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940611	AATTAAAGAAAAAAA[A/C]TAAAGCCATTGGACA	54813
rs556150734	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941138	AATAAACAAAAAAAA[A/C]CTCATGTCTCTCTCT	54813
rs556164744	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44979585	ACTCTTAAATAGCAC[C/T]TACTCTATGCCAGGC	54813
rs556536411	snp	A/G			missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964304	ACTGTCACTGTGGTG[A/G]CCACGTGAGGGATAG	54813
rs556555855	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44966412	CAGGAAGCAGAGGTT[A/G]CAGTGAGCTGAGATC	54813
rs556575027	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44952015	AGGCACACATCACCA[C/T]GCCCGACTAGTTTTT	54813
rs556575136	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967226	ATATTAATACCTCCA[A/T]TTCAAAACTAGTACT	54813
rs556621399	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44948172	AGAAAGCAGTCCTCG[-/T]TAACTTTACCTTCTC	54813
rs556632410	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950419	TAATTAGGAATCACA[C/T]AGTGATAGATCCTAT	54813
rs556792002	in-del	-/TATT			intron-variant	KLHL28	GRCh38.p7	14:44936035	TAGTTACAGAATTCC[-/TATT]TAAAGTCAGTTTTTA	54813
rs556793080	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958519	ACAGTTCAACTTTCC[C/T]CATAGGATAATTCAA	54813
rs556830189	snp	A/C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44965849	GTATCATTTATTACA[A/C/T]TGGGGGCTTACAAAT	54813
rs556990690	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44968906	TGTTCTCTACATGTA[C/T]ATTCTTCCCTCTCTC	54813
rs557025437	snp	C/T	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44970503	GAACAAAGACAATTT[C/T]ATTTCTTCCCAATCT	54813
rs557038474	snp	C/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44953735	TAAATTCCTTTTACT[C/T]ATAAATTATCCAGTT	54813
rs557121670	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44929944	AGGCTATTTTTTTTT[A/T]ATTTCATTTCATTCT	54813
rs557187823	snp	A/C	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44944968	TAAAATATAGAAAAT[A/C]TGCACATTTAAAAAG	54813
rs557202896	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969439	TTACAGGTGCAAGCT[A/G]CCACGCCTGGCCTAT	54813
rs557273761	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962061	GTTCTGACTTCCTCT[C/T]CCAGGAGACTTTGGC	54813
rs557309124	snp	A/C	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44953560	GAGAGCTGAGCTAGC[A/C]CACTCACAGCCCCCT	54813
rs557316213	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926315	ACTGGTGTATGGCTC[C/T]TACTACTACTGCCCA	54813
rs557405649	snp	A/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964198	GAATATGCAGTACTG[A/G]TGCCATCTTCTGCCG	54813
rs557436797	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977842	TTTAGTAGAGACAGG[G/T]TTTCACCATGTTGGC	54813
rs557467436	in-del	-/ACC	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44953277	AGATTTCTGCTACAT[-/ACC]ACCTACACCAACAGG	54813
rs557497839	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44947271	GAATGCTGGCAGTCA[C/T]CAGAAGCTAGAAGAG	54813
rs557526935	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44933766	AAATTTCTACTTCTT[C/T]ATTCTATTAAGCAAT	54813
rs557548206	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44967289	ATTTGAATCTCCCTT[C/T]GTTCACAATAAAATC	54813
rs557586416	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44973868	GTTTCTGAGAAGTTA[A/G]ATGTAATTCTTATCT	54813
rs557595198	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44957787	CTCTGTCTATGTAAT[G/T]CTTAAATATTCTATT	54813
rs557615927	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44947196	AGACGTGACACAGAC[A/G]GAAGAGGAGGTCATG	54813
rs557697447	snp	C/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44977338	CTTCCGGGTTCACGC[C/G]ATTCTCCTGCCTCAG	54813
rs557852129	snp	C/T	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44966627	TTTTTTTTAACTTTT[C/T]CATGATAAAATTGTC	54813
rs557864952	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937194	TCTGTCGCCCAGGCT[A/G]GAGTGCAGTGGCGCA	54813
rs557901085	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944436	ACTGTTTGGTCTTTT[A/G]TAGAAAAAGTCTGAC	54813
rs557967126	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941989	CATAGTTTTAATTCA[C/T]ACCTCTAAACTATAC	54813
rs558019158	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977140	GCATCTAACTCTTCA[C/T]ATTCTGCTTTATATA	54813
rs558033799	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952063	AAGGAGTTTCACCAT[C/G]TTGCCTAGGCTAGTC	54813
rs558055997	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44941683	ACCAAAAGTCATTAT[C/G]TTCTCCATAATGCCA	54813
rs558192254	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44937900	TCACTCCCACCATAA[C/T]GGTATTAACCCCTTC	54813
rs558326524	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941107	ACCTGGGCGACAGAG[C/T]GAGATGCCGTCTCCA	54813
rs558375364	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977985	ACTGGGCAGCACCAC[A/G]TGAGCTGATTTAAGG	54813
rs558375616	snp	A/G	4.97475e-05	0.00498711	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963564	GCAGGTGCTGGGAAA[A/G]TTTAACCCTAGTTCT	54813
rs558395229	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943876	TGCAACACCACTCCC[A/G]GATAATATTTTAAAT	54813
rs558402576	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44939702	TTTACTGTGCACATT[C/T]CTATCAACATTCTGA	54813
rs558437510	snp	A/G	6.59044e-05	0.00574002	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964082	TTTTTAAAGCTGTGG[A/G]TACAGTTGAACTGCA	54813
rs558522689	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44940501	CTTATGACTCCTTAT[A/G]TATAAGTAGAAACAA	54813
rs558562615	in-del	-/TAAAGTA			intron-variant	KLHL28	GRCh38.p7	14:44948554	CTGAAAGTGATTCTC[-/TAAAGTA]TAAAGTTCTACAAAA	54813
rs558646759	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931741	CAAGGTGCAATTCCA[C/T]ATGCTATTCCATTAT	54813
rs558784872	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44980200	GGCTCTCTGCTTTAA[A/C]ATTTACAGTCCACTG	54813
rs558969511	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972351	ATGTGCAGTCTGTTG[C/T]TGGATAAAGTAATCT	54813
rs558980686	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950278	AACTTTCTATGTTGC[A/T]CTACCTCTCACTATT	54813
rs558998090	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936691	TCCAGTTACATTCTG[A/C]TGCTCAGATGTAGCC	54813
rs559014392	in-del	-/ACA	0.00199481	0.0315187	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937600	TTTAGCTAAATACAT[-/ACA]ACATACAATGTCATT	54813
rs559024207	in-del	-/AG	0.00597247	0.0543191	intron-variant	KLHL28	GRCh38.p7	14:44946012	TAGTACAGAATAATC[-/AG]ATTTGTAATTTATTT	54813
rs559038463	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957366	TTTGAATAAGACAGT[G/T]TTAGAATCCTAAGTT	54813
rs559129654	snp	C/T	0.00478085	0.0486577	intron-variant	KLHL28	GRCh38.p7	14:44952192	TTTTAATTTGGCCCC[C/T]TTCCTCTCTCAAAAA	54813
rs559148892	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978865	GCATGGTGGCATATA[A/C]CTATAGGCCTGTAGT	54813
rs559154302	snp	G/T	3.74553e-05	0.00432738	intron-variant	FAM179B	GRCh38.p7	14:44964489	TTCTCTAATTTTCTT[G/T]AGTCGAAAGTGTGAA	54813
rs559189388	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44931116	AGCAAGTTTGAGAAA[A/C]AATAATATGCACATT	54813
rs559214926	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932397	CTCAGGAATTTGAGT[C/T]AAGACTGTGTTTCAG	54813
rs559281571	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961524	TCTGCGGCCGGAGGG[G/T]TAAGAGAAGTCGACA	54813
rs559314851	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44949713	TTAAAAGGGATAAAT[A/G]TAAAAATTCTATAGC	54813
rs559518939	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927808	GCCTAGTGCTTTATA[C/T]TTAATGCATATATTT	54813
rs559545995	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966835	TGGTGCAGGCCTGTA[C/G]TCCCAGCTACTTCGG	54813
rs559557728	snp	A/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937428	CTGGGATTACAGGCG[A/T]GATCCACTGTGCCCG	54813
rs559613093	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968538	CAGGCGTGAGCCACC[A/G]CGCCCGGCCTGGACT	54813
rs559678634	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44964813	TTCTGGGAATGAAGA[C/T]GAGGCCAGTTTCACA	54813
rs559702900	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44959877	TTAAATACAAAAGGC[C/T]TTTTAAGTCAATATA	54813
rs559705091	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967428	AAAGTTTAAGATTTC[A/G]TTACAGTTCTTTTTG	54813
rs559733197	in-del	-/TAATT	0.00159617	0.0282053	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925742	TGATACCACTTCCTA[-/TAATT]TAATATTCACTCACA	54813
rs559751472	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44968614	AGTACAGATAGTTCC[C/G]ATATACCCCTGTCCA	54813
rs559759375	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940956	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCATA	54813
rs559826587	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975186	AGCCACTTTGACACA[A/G]ATCAACTGAAAACAT	54813
rs559835396	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44965400	GTTAATGTCCCTTGT[A/G]ATTTTATCTAGAATA	54813
rs559947874	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940679	AGCCAGTAAACCTCA[A/G]TTGTCTTGAGGCATA	54813
rs559989213	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975728	TGCCTCAGCCTCCCA[A/C]AGTGCTGGGATTACA	54813
rs560123019	snp	C/T	0.000270211	0.0116203	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931337	ATTCTTATTACCTGT[C/T]CTAGGTTCTTTCATT	54813
rs560175870	snp	C/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44957961	ATACAAAAATACACA[C/G]GGCTTTAAAATGAAA	54813
rs560277443	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44958035	CTAAAAGCAGATTTG[A/G]TATATCAGGTTCCTC	54813
rs560291822	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931930	TGAGGATAGTGCAAC[C/T]TGAAGGGATTCATAT	54813
rs560361251	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978342	AGCTGATATTATCAT[C/T]TAGTCTTTTTCAGTG	54813
rs560488829	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44935092	CAAATGTTTATCCAC[C/T]ATAAAATGGATAAAT	54813
rs560536128	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924900	TTTTATTTGACTCCA[C/T]ATTCACACCAGTAGG	54813
rs560564424	snp	A/G			upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962102	CACCTGACGTGGACT[A/G]CATAACCCAGCATTC	54813
rs560600702	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972902	GTTCAACATCATTTT[A/G]CTATAATGTTGATGA	54813
rs560633500	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950524	ACATAGGTCTGTAAA[A/T]ACACACATACATGTA	54813
rs560737381	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942207	CCCATGTAATCATCT[A/C]ATCAAAAGAACTCAT	54813
rs560774399	snp	C/G	0.00597247	0.0543191	intron-variant	KLHL28	GRCh38.p7	14:44941550	AGAGAATTGCTTGAA[C/G]CTGGGAGGCGGAGAT	54813
rs560791726	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44970217	TCTTTGATATCTTGC[A/G]TTGGAGTTCTATACT	54813
rs560928944	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44954566	GTGATCTCCCTGATC[G/T]AAGCAAAGTGTGTTT	54813
rs560930188	snp	C/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925629	TCTCTCTAGCTCCCA[C/G]AGCATCTAACAGAAT	54813
rs560962900	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44976990	GCTCAAAATTGCTAA[C/T]GATTAAAAGCAGAAC	54813
rs560972893	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953144	GAAAATATAAAAGTA[C/G]ATCATTTAGATATGC	54813
rs560999749	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975920	AGTATTGAGAGTGCC[A/G]TGATTTATAAAATCT	54813
rs561006383	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44930054	ATTCTACTTTAGATA[A/T]TATCTTATATAGTTC	54813
rs561019788	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948046	TTGATCTTTTTAACC[C/T]ATGTAACTTCTTTTA	54813
rs561054533	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947525	GGAATACAGGTCATG[G/T]ATACAATATAAGCTA	54813
rs561138324	snp	A/C	0.000399281	0.0141238	missense	KLHL28	GRCh38.p7	14:44945652	CAGTCCCTGTATAGG[A/C]ATACTCCACAATGGC	54813
rs561313920	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44943248	ATATAATTTACTTTA[C/T]GCCAGTAACCAGTGC	54813
rs561383336	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955762	CTGCACTCCAGCCTG[A/G]GAGACAGAGTGAGGC	54813
rs561424911	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943237	AATATTTACTAATAT[A/G]ATTTACTTTATGCCA	54813
rs561493895	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44977447	TTCACCGTGTTAGCT[A/G]GGATGGTCTTGATCT	54813
rs561558365	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44933669	ATACATGTATGATTA[A/C]AGGAAAGAATTCAGA	54813
rs561558477	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44946067	CTTCATAGTAAATAC[C/T]AGAACTAGAGGCTTT	54813
rs561591900	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970621	TTGCCTTGTTTCTAA[C/T]CTTAGTGGGAAAGTT	54813
rs561721901	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44968604	TTCAACAGAGAGTAC[A/G]GATAGTTCCCATATA	54813
rs561762867	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924832	AGTAAAGATGTATAA[A/T]ATAAAAGACATATGG	54813
rs561823941	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966741	GGACGATTGCTTGAG[C/G]CCAGGAGTTCGAGAC	54813
rs561871195	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968470	AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT	54813
rs561908809	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44931658	GAGAGATATTAAACA[A/G]GAGTAGTCTGCCACA	54813
rs561986089	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943953	ACTCCAGTCTCAAGT[G/T]ATCCTCCTGTGTTGG	54813
rs562026484	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961429	TTCCATATTATGTAC[A/G]TTGTAAAGAAAACGC	54813
rs562038287	snp	A/G/T	0.00557734	0.0525397	intron-variant	FAM179B	GRCh38.p7	14:44966112	ACTCCTGACCCACCC[A/G/T]CCTCGGCATCCCAAA	54813
rs562043115	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44974454	TAATTATAGTTTTAG[A/G]AAATTCTGGTATGTT	54813
rs562162010	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44964754	TTTATCTCATTCATA[A/C]AACAAACATTGAATA	54813
rs562180774	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978115	ATCGTTATAAGTTTT[C/T]AAAGATATGTGTATG	54813
rs562212480	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926943	ATTTAAAACTAAATA[C/T]GTGATGAATCTATTT	54813
rs562247502	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936600	AAAGAATAAACTGAT[A/T]AAGGAAATGTAGAGT	54813
rs562308315	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970776	TGTCTAATGCTTTTT[C/T]GCATCTATTGATATA	54813
rs562348435	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44935254	CAAAAACAGGTAAAA[C/T]GAATCTCTGGATTAG	54813
rs562380586	snp	C/G	0.00557542	0.0525036	intron-variant	KLHL28	GRCh38.p7	14:44947333	AAGGAGCATGGTCCT[C/G]CCACCTTAATTTTAG	54813
rs562404523	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44946642	GCTCACTGCAACCTC[C/T]GCCTCCTAGCTACAA	54813
rs562584079	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939286	CTACAACGGGAGGTA[C/T]AGCCTCAAAGATCTT	54813
rs562592416	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44964733	TTAGTTACTGTAGCA[G/T]GTCAGTTTATCTCAT	54813
rs562767229	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931130	ACAATAATATGCACA[C/T]TGGCATATAAAAGTC	54813
rs562803374	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44939999	GTAATTTATAAAGAA[C/T]AAAAGTTTATTTGGC	54813
rs562804599	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44975576	GGTTCAAGCCATTCT[C/T]CCACCTCAGCCTCCC	54813
rs562893182	snp	C/T	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44965264	TGCACCTAAGACTAT[C/T]AGTAGTAATTCAATA	54813
rs562928079	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44942227	AAAGAACTCATTCAT[C/G]TTGGATTCCTCCCTC	54813
rs562933121	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44979318	TCCAAGATCAAGGCA[C/T]TGGCAAATTCAGCGT	54813
rs562942818	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941429	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTCAGC	54813
rs562976054	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44942019	CTATATGCTGATGAC[C/T]TTCAAATTTCCAGCC	54813
rs562976415	in-del	-/A	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44950777	GGTACATAAGCACTC[-/A]GTAATTGGTAGACGT	54813
rs563024072	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44956774	TGGATTATTAATATA[G/T]TAATTAATCACTGCT	54813
rs563152444	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44949279	CGATAAGAAGATGTA[C/G]AGATCTTTAGGATTA	54813
rs563159262	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44938527	CAGGCGCCCACCACC[A/G]CGCCCAGCTAATTTT	54813
rs563171951	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44929591	ATATAGGGTTTGGTA[A/C]TATCTGCAGTTTCAG	54813
rs563189470	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948374	TAGAGATAAAACATA[A/T]CAGTGAAGAACACAG	54813
rs563361565	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44938464	GCAAGCTCCGCCTCC[C/T]GGGTTCACACCATTC	54813
rs563398512	snp	A/G	0.000131911	0.00812022	missense	KLHL28	GRCh38.p7	14:44945573	CATTCTTTCAGGACA[A/G]GTTTTATCTGGAGTA	54813
rs563422065	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946835	TGCGGGGATTACAGG[C/T]ATGGGCCACCACACC	54813
rs563455044	snp	A/C	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44954912	TTCCAAATAACTTTA[A/C]AACAGTAATCTGAAG	54813
rs563525829	snp	A/C	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960723	CCACCCCCACCCCCC[A/C]AAAAACAAAACAAAA	54813
rs563554723	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953013	TAATAGCTGGGCTAT[C/T]TGATACTTGGGCAAA	54813
rs563564651	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928973	AAACTGGGCCATCCG[A/G]ATGTTCATGCAGTAC	54813
rs563586991	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935359	CTGTTTCTTGAACTG[A/G]TTTGTAATGTTTACT	54813
rs563590951	in-del	-/AG	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44957308	AAATTTTGCACAGTA[-/AG]AGACTTTTTTCTTAA	54813
rs563593453	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952237	AAATGCACAGAATTC[G/T]AACATTTTCAAATAT	54813
rs563593540	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961340	GTCCCACAGAGGAAC[C/T]GCATTAGAAGGAAAG	54813
rs563816431	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962227	CGGTGGCAGCTGTGG[G/T]GTCTAGGGCTCAGAC	54813
rs563817302	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959752	GCAATTTTCAATGTA[A/T]CCTTAACCACTTCCT	54813
rs563836843	snp	G/T	0.00279162	0.0372561	intron-variant	FAM179B	GRCh38.p7	14:44975805	TAATGAAGTGGGTTT[G/T]AACCATTTTTTTTTT	54813
rs563909099	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44940154	GCAGGACTTATCTTA[G/T]TATCAGGAGCCCACT	54813
rs563974040	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932709	TTGAAGAAGAGTTGA[C/T]GCACTGCAGCAAGAC	54813
rs563997750	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44969771	TTTTTTACATGTGCA[C/T]GTTCAGTTGTTGCAG	54813
rs564122371	snp	A/C			intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937531	TTCTCAGTGATAGTA[A/C]GACTAAAGGTTATGA	54813
rs564122608	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978525	AAAAGAAGATCAAAA[A/C]CAGGAGCAGTGGCAC	54813
rs564188710	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950624	ACTGGGCTTTGGTAC[C/T]AGGCTTCCCGGGTTA	54813
rs564217963	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972747	TCTTTACTTTTAATT[C/T]ATATCTATCTTTATA	54813
rs564337751	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44957218	ATATAGATGGTGTCA[C/T]GAGTTGATAACTATT	54813
rs564338768	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44979251	AATGTCTTAGACTGG[A/G]TAATTTATAAACAAT	54813
rs564434298	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972167	ATTACAATTTGAAAT[A/G]AGATTTGGGACAGGA	54813
rs564451575	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44974351	TTCTAGGTTTCTTTT[A/G]TGTTCCTTCTTAGAA	54813
rs564499083	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925858	CCAATGATTATTGAA[C/T]AGCCAAAGGTGCCTA	54813
rs564540076	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936517	CATCTTTTCAGTAGA[A/G]TAAGAGGTAAGGGGA	54813
rs564627453	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943113	GTCAAAAGATATGAA[A/C]AGGTCTTATTATTCT	54813
rs564682768	in-del	-/G			intron-variant	KLHL28	GRCh38.p7	14:44932014	AGACTTTTTTTTTTT[-/G]GTTCCTAAATTTTAT	54813
rs564693751	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44977130	GCTATCAAATGCATC[C/T]AACTCTTCATATTCT	54813
rs564800938	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928922	TTCATGCTACTTCAA[A/G]TTAAAAAGAAAGCAA	54813
rs564861246	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44970032	TTCTGGGTTTTTTGC[C/T]TCTCTGTATAAACTT	54813
rs564893598	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44951005	CTTATTAGATTTAGA[C/T]AGTTTATTACTTACA	54813
rs564908013	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44930134	GCTTTCCCTCTCAAG[A/G]ATACAAAAGAAACAA	54813
rs564931810	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44954267	CCTTTGACCCAAAAA[-/C]CCTACTTCTAAGAAT	54813
rs564935641	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44950012	AGCAGAAATTCAAAT[A/C]ATGTCTTACAGGTAA	54813
rs564963057	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977487	ATGATCTGCCCGCCT[C/T]GGCCACCCAAAGTGC	54813
rs564985779	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970682	TATGCTTTCTTGTAG[C/T]GTTCGCTATAAAGTT	54813
rs565002074	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44929582	ATATTACATATATAG[A/G]GTTTGGTACTATCTG	54813
rs565040716	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44932448	GCTGCATTATGGAAT[C/G]CAAATTAAATCAGAA	54813
rs565151200	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939247	GATTCCCCCAAACCA[C/T]TCTGCCCTCCTAGTG	54813
rs565196120	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946696	AAGTAGCTGGGATTA[C/T]AGGCACCTGCTAACA	54813
rs565197182	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44942758	ACACTCAACTTGTAC[A/G]TGAAGTTCTCTACAA	54813
rs565292103	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971386	TTTTAATGTTTATGT[G/T]ATTTGTAGTGATAGT	54813
rs565327771	snp	C/T	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44948290	GATCAAATCAGACAA[C/T]GTACATAAAAACATG	54813
rs565364067	in-del	-/G	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44932543	GCACAAAGGCACAGA[-/G]GTAAGATTGTTGGGC	54813
rs565386539	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943285	GAATAAGAGTTAAAC[A/T]ATCAATTCGTGTAGC	54813
rs565389231	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940817	TATCTTTACCCTATC[C/T]CTCTTTACTTATCTC	54813
rs565416988	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947626	TCTTAAAACCATCAA[A/T]TCTATAAATTCAAAC	54813
rs565435000	snp	A/C	1.64923e-05	0.00287156	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963816	CAAGCTAATGAAGGA[A/C]GTAGGACCTCAGCAG	54813
rs565449282	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44935332	GGGTGGCTTTTGAGT[A/G]TTGGTCATACTCTGT	54813
rs565504759	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44970559	CTTATTGCATTAGTT[G/T]GAACTTCCAATATGA	54813
rs565562313	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44956606	GTGAAAAATCTTGTA[A/G]AATAAACTAAATTCT	54813
rs565625168	snp	A/T	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44942547	GTCTTTTTTTTTTTT[A/T]AAATCATGGCATACA	54813
rs565888629	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952581	AGGCTGGAGTGCAAT[A/G]GCCACTCAAAGGCAT	54813
rs565903452	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44967212	TTTTTAATGCATTTA[C/T]ATTAATACCTCCAAT	54813
rs566056991	snp	G/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44944399	CACAAAGATTACATG[G/T]CTCACAAAGTCTAAA	54813
rs566061777	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967843	CCCAAAACTTGTAGA[C/T]TTTTTTGGAAATAAT	54813
rs566146926	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44939253	CCCAAACCATTCTGC[C/T]CTCCTAGTGTTCTGA	54813
rs566186694	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953223	CGTTTAAATAAATGT[A/G]TTGAGATAACGGAAT	54813
rs566300637	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44970286	GATTGAAATATCCTA[C/T]TTCTGTATGTTAATG	54813
rs566381448	snp	C/T	0.0166325	0.0896639	intron-variant	KLHL28	GRCh38.p7	14:44939464	GTCTTTCTGTTCCGC[C/T]TACCATTTAATTATA	54813
rs566426893	snp	A/G	3.29478e-05	0.00405867	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964005	ACGCAGGGTACGCCA[A/G]GCAGCTTTAGAAGCT	54813
rs566427432	snp	C/T	0.00517822	0.0506191	intron-variant	KLHL28	GRCh38.p7	14:44948491	TAATCTAAGTATTAA[C/T]TGTTTCATTCATAAA	54813
rs566463683	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970883	GCATACCTGGGATAA[A/T]TTCCACTTGGTTGTG	54813
rs566477271	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44976525	ATTTTAATCTTAGTA[C/T]CCAGTATCTTTAGCA	54813
rs566608611	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44978037	TTTATAATTGCTAAC[A/T]TGAGATTTTGAGGAT	54813
rs566666363	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977306	GTAGTGTGATCTCAG[C/T]TCACTGCAAGCTCCA	54813
rs566786298	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924097	CTGGTCTCAAACTAC[A/T]GACCTCAGGTGATCT	54813
rs566863099	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44935413	CATTTGGGATTTGTA[A/C]ATTTTTCTGCATGTG	54813
rs566877414	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971808	CTTGTATGTAACTTA[A/G]AAGTGTATTTAGTCT	54813
rs566964869	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966173	CCCAGCCCAAATTGT[A/G]ATTTTTAAATTACAA	54813
rs566973690	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44951696	ATATACTTTCATTCC[C/T]TGTAAGAACTACTGA	54813
rs567003577	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44965777	ACTTTGAGACCCTAA[G/T]AATACCCCGACAACT	54813
rs567110790	snp	A/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44978836	AAAAAAAGAAGAAGA[A/T]GATCAAGAGCCAGGC	54813
rs567121592	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44932284	CCTTTATTTTTTTTC[A/G]TCACAGGAGAATTCA	54813
rs567140035	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44932853	GGCAAAAAATATAAA[A/T]AAATAAAAGGAGGAA	54813
rs567244294	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961936	TAGCTCCGGTCAAAC[C/G]CTAACTCTTACGGGT	54813
rs567286566	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928431	AATTGTCTTAAAAAT[C/T]TATTACATCCGTAGC	54813
rs567325338	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44944880	AATAAAAACAATCAC[A/G]TAAGTATTTTAGGAA	54813
rs567367715	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44938870	GTTGCACACTACTTG[A/C]ACTACAGTTCTGTGT	54813
rs567402132	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968714	TTAACATATAATTAT[A/C/T]ACCCAAGGCCCATAG	54813
rs567417418	snp	A/C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927395	TAGTCTAGAACATTA[A/C/T]GGCACTTAAGAATAT	54813
rs567427230	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939422	TACCTTTTCACTTTT[C/T]ACATGGTCAAGCTGC	54813
rs567458129	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936780	AAAGGGGCCATGGCG[C/T]ATTTAAAGGAATGAT	54813
rs567539370	snp	G/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937657	TCTTAGTTCATTTTC[G/T]GCCGATATAACAGAA	54813
rs567600921	snp	A/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44946088	TAGAGGCTTTCAGAG[A/T]TAGAAGAGATTTAAC	54813
rs567709921	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953393	GAAATTTAGTCCCCA[A/G]TGCGGTAGTATTGAG	54813
rs567720003	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44930390	ATGCCTCAGCCTCCC[A/G]AGTAGCTGACACTAC	54813
rs567755235	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44930024	TATTAAATGACATAA[C/T]TTATGCTTCTAAAAA	54813
rs567764745	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950753	TGTAAATATGCCTTT[C/G]TATGTGCTGGTACAT	54813
rs567775963	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44977335	CACCTTCCGGGTTCA[C/T]GCCATTCTCCTGCCT	54813
rs567907974	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925762	TAATATTCACTCACA[C/T]TTAAAACAATAACAG	54813
rs567973020	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954477	ATGGTTGTGAAAACT[A/G]TAGAGCATCCACACA	54813
rs568042374	snp	C/T	6.59261e-05	0.00574097	synonymous-codon	KLHL28	GRCh38.p7	14:44934393	ATTCCAGCATTCCAC[C/T]GAATTTTCATGTTTT	54813
rs568124276	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44965633	TACATTATGAGGCAA[A/G]TGATATCAGGCTGTC	54813
rs568155525	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44933456	ATTAGGATTACAGGC[A/G]TGAACCACCACACCT	54813
rs568207733	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957267	AATAGATGTTCATCA[C/T]ATTGTTCTGCTTTTA	54813
rs568286767	snp	A/T	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44973263	TTTAAATTACTTTTT[A/T]TTAGTAGTTTCCCTA	54813
rs568429356	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44956630	AAATTCTTCAACAAA[C/T]AAACTGCAAGAAATA	54813
rs568450420	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44973759	TCTTCACTTGTGAAA[A/G]ATTATTTCCCAGGGT	54813
rs568550110	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943713	AATAAAATGTATTAT[C/T]GGACTTTTTTTTTTT	54813
rs568603519	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925051	TTGTTATCTAATTAA[A/G]TCATGTCTAATTAAA	54813
rs568686063	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44976251	TCCTTATTCGTTGCC[C/T]ATCTACATTTAACCT	54813
rs568771194	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966434	GCTGAGATCACACCA[A/C]TGTACCCCAGCCTAG	54813
rs568855897	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44978972	GATCCCATCTCTCTC[C/T]CTTTTTTTTTTTAAT	54813
rs568964998	snp	A/G	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44947217	GGAGGTCATGTGACT[A/G]AAGAGGCAGAGACTA	54813
rs569000178	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44955372	AGAAACTGACCATCC[C/T]GGTAGCAAAGAACAC	54813
rs569060960	snp	C/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44930297	CTCCAACATTTGAAA[C/T]TTTTTTTTTTGAGAT	54813
rs569074667	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44929498	TATTCTATTATTGTT[A/G]TTGCTAATCTCTTAC	54813
rs569132734	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44958212	CTACAGTAACTTAAC[G/T]TTAGGCTCTGAAACC	54813
rs569264725	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977896	CTCAAGCAATCCTCC[C/T]TCCACTGCCTCTGAA	54813
rs569300929	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978678	TGGCACATGTCTATA[A/G]TCCCAGCTACTTGGG	54813
rs569338807	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44970474	CTTTCTATGCAGACA[A/G]TCATGTCATCTGTGA	54813
rs569353555	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926334	TACTACTGCCCAAGA[C/T]ATTTCACATTTAGTC	54813
rs569376456	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44935914	TATATCTTTACCCTC[C/T]CCCCGCAAAGTTGGG	54813
rs569413556	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927204	TCATAAAGCATGATA[C/T]TACATTTATGATTAA	54813
rs569418564	in-del	-/TTTCTTT	0.00636936	0.0560724	intron-variant	KLHL28	GRCh38.p7	14:44933310	CTTTTCTTTTCTTTC[-/TTTCTTT]TTTTTTTTTTTTGAG	54813
rs569427094	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947710	GGAAAAAATCCAACT[C/T]TTGAAATTTTTATCT	54813
rs569504325	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44939511	CATTTCTTCCCTCTC[A/G]CACCTTACTATATGC	54813
rs569608686	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974023	TTCTCCTGGTTTTTC[G/T]CTGAGTTTCCTAGAT	54813
rs569687983	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974673	TATAGTGCTTTAATT[A/G]CACTTTTGATGAGCG	54813
rs569788070	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942679	TAATGTATCATGCCA[C/T]TGTGTCTTTGTACAT	54813
rs569817221	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44951792	TCAACAAGGCAAGGT[A/G]AAAATAGGGAACTTA	54813
rs569830076	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44935919	CTTTACCCTCCCCCC[A/G]CAAAGTTGGGAAAAA	54813
rs569904675	snp	C/T	4.9445e-05	0.00497193	synonymous-codon	KLHL28	GRCh38.p7	14:44945155	CATAAAGTGGTACTT[C/T]AGGGCTTCATTCAAA	54813
rs570070806	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44938028	GAACACTTTCAAACC[A/G]TAGAATTTTGCCCCT	54813
rs570156714	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44968092	CTTTTGAAAGATGCT[A/G]TGGTGTAATTAAAAC	54813
rs570257404	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44973694	ACAAGGCAGGTCTTA[C/T]TAACAACAACTTCTT	54813
rs570264367	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975244	TGAACTCAATGGATG[C/G]CCCCCCACCAGGTGA	54813
rs570407116	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957153	GTAGATGAAATAATA[C/T]GTTGTTAGGATTTGC	54813
rs570471547	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44949813	GTTTAGGGATTTTAA[C/T]TGCAGTACTATTTTA	54813
rs570519919	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971709	TTCCTCTAGGCACCG[C/T]TTTCACTGCATACCG	54813
rs570538550	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932417	CTGTGTTTCAGAGAA[C/T]GTGTGGCATTTCTAA	54813
rs570629002	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971003	TGTGGGGTTTTTGTT[A/T]TGTTTTGTTTTTGTT	54813
rs570778401	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44932031	TTCCTAAATTTTATT[C/T]ATTTATTTTTGAGGC	54813
rs570909969	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44947434	ACTGAGTTTGTGTAA[C/T]TTGTTACAGTAACCT	54813
rs570946763	snp	G/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44959956	AAAAAGAATACACAC[G/T]CAATGAATGAGATTT	54813
rs570946800	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950988	TTTTAAAATATAGAT[A/G]GCTTATTAGATTTAG	54813
rs571207787	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962316	AAGCTGTTCTTTTGC[C/T]TCTTCTGCAGCTTGG	54813
rs571256234	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44935005	TCTACTGATGAAAAA[G/T]GCATGCATACATATA	54813
rs571345516	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44930595	TTTTGAGCACCATAT[A/G]ATGCTCAAAGAAAGT	54813
rs571358553	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954611	TATCTACGATAGGGA[A/C]GATTACAAACATACA	54813
rs571408461	snp	C/T	4.96981e-05	0.00498463	missense, intron-variant	KLHL28	GRCh38.p7	14:44931516	CCATCTCCCAGGAGT[C/T]CTTACTTGGATCATA	54813
rs571433374	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972080	GATAACTCACTATTA[C/T]GAGAACAGGAAAGGG	54813
rs571490154	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44938670	CCACCGCGCCCGGCC[A/G]AAAACATTAAGTCTT	54813
rs571532756	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925345	ATACTACAGGAAATA[C/T]ATATATTTAAAATTT	54813
rs571575210	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44977328	CAAGCTCCACCTTCC[A/G]GGTTCACGCCATTCT	54813
rs571577007	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928600	AAGCAGTATCAGCAC[C/T]CTGTCCATTCATTCA	54813
rs571700664	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946218	TTTGGATCAAAACTT[C/T]ACCAACTTTTTCATT	54813
rs571713401	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44973431	TCATTCATTTCATTT[A/G]TACATAAACACACAG	54813
rs571732625	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942325	TTTTTAAAATGAATG[C/T]CCCATTCTCTATCTT	54813
rs571785825	in-del	-/A	0.0126979	0.078662	intron-variant	KLHL28	GRCh38.p7	14:44952760	ATTTGGTTCTCAGCT[-/A]TCTACCCATAAATGG	54813
rs571824605	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955286	GCTATACATACATAT[A/T]AAATATACGTAATAT	54813
rs571861283	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941295	GTATTCACTTCTAGG[A/C]CCACTGTAATGTATC	54813
rs571994403	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44933737	CTATAATATTGTATA[A/G]ACACACAGGAATTAA	54813
rs571995348	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924445	AAGAATACAATTCTT[A/T]ACTAGTTAAATGACA	54813
rs572031238	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941973	ACTCCATCAAAGACT[G/T]CATAGTTTTAATTCA	54813
rs572308713	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44966591	ATGTGTAATAATTAC[A/G]TATTATTTTTTGTTA	54813
rs572351733	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44979070	TGAATTTTGATATAA[C/G]AATTAGGAGTCAAAA	54813
rs572423521	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44935094	AATGTTTATCCACTA[G/T]AAAATGGATAAATTG	54813
rs572709200	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969686	ATAGTTTTACAATTT[A/G]CATTTAAGTCTATGA	54813
rs572776374	in-del	-/T	0.0123036	0.0774623	intron-variant	FAM179B	GRCh38.p7	14:44966354	GGCACACACCTGTAA[-/T]CTCAGCTACTCGGGA	54813
rs572840519	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44933988	AATTATATCCATGGA[C/G]CAGATTAAGTTTCCC	54813
rs572882092	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44930880	GATTTGTTTTGTTTC[C/T]ACGAACTCTGAAATA	54813
rs572952711	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44968494	ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	54813
rs572956825	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962186	GGAAGCAATCGGTTT[G/T]GTCACGTGGTGCCCT	54813
rs572963930	snp	C/G	3.68922e-05	0.00429473	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962451	CTCCGCGCTGCTTCT[C/G]CTGCCGCCCTTTCCA	54813
rs573113528	snp	C/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44949129	CTGCAAATGAGATTA[C/T]TGAATCATTACCAGT	54813
rs573125885	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954856	TTGAAAATTGAAAAT[A/G]CAAAGGAAGAAAATA	54813
rs573156626	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44956454	CTCACGTCCCAACCC[C/T]AACACACACCAAAGT	54813
rs573173105	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946502	TCCAAAGTCCCATGA[G/T]GGCAATAAGGCTCAC	54813
rs573279665	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44964526	AAATGAAAATATGCC[C/T]GTGATGACTTAAGGG	54813
rs573286055	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44957338	AAAAAACAGAAAATA[C/T]AAGGCACAAAATTTT	54813
rs573368882	snp	A/G	0.0166325	0.0896639	intron-variant	FAM179B	GRCh38.p7	14:44977472	TGATCTCCTGACCTC[A/G]TGATCTGCCCGCCTT	54813
rs573452511	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925518	CTAATCACTTCTTAC[A/G]ATGTCAGAGATAAGG	54813
rs573525712	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931641	TAAAAGTTCACATAA[C/T]AGAGAGATATTAAAC	54813
rs573529365	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960550	TCACCTCCCTGTCTT[C/T]AACCTGTCCCTAAAA	54813
rs573675984	snp	C/T	0.0126979	0.078662	intron-variant	KLHL28	GRCh38.p7	14:44952762	TTGGTTCTCAGCTAT[C/T]TACCCATAAATGGCT	54813
rs573679624	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975667	AGACAGGGTTTCACC[A/G]TGTTGGCCAGTCTGG	54813
rs573686703	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967411	CCAACTACCTACTAA[A/G]TAAAGTTTAAGATTT	54813
rs573712791	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961241	GCAATCTCTGTCTCT[A/G]GGAGACTGAAAGGCT	54813
rs573838816	snp	A/C	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44969097	ATGGTTTGATACCTC[A/C]TTTCTTTCTTTCTTT	54813
rs573887331	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926620	CAAGTGATTCTCCTG[A/C]CTCAGCCTCCCAAGT	54813
rs573907160	snp	C/T	0.00105452	0.0229379	missense	KLHL28	GRCh38.p7	14:44945195	CAAGTGCGATCATCA[C/T]GAATAAGATGATTTG	54813
rs573927719	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927540	CAAGTACCGACATAA[C/T]AATAAAATGCAAGTG	54813
rs573981218	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44938106	ATCCCAATAGCCCCA[A/G]AAGTCTTAACTCATT	54813
rs573990920	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977285	TGTTGCCCAGGCTGG[A/T]GTGTAGTAGTGTGAT	54813
rs574019823	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937369	GGCCAGGCTGGTCTC[A/G]AACTCCTGAACTTGT	54813
rs574027612	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928863	TAATCAAGAGCAACC[A/G]AAACTACTTCTCAAT	54813
rs574110751	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978977	CATCTCTCTCTCTTT[C/T]TTTTTTTAATGTCAC	54813
rs574345780	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44959680	CATTCCTATAATTCA[C/G]TAATTTAACTACATT	54813
rs574496201	in-del	-/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928804	TGGCAAAGTCTTTAC[-/T]TTTTTTTTTTCTCTT	54813
rs574761746	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44942732	TCTGCTTGATTCTTG[A/C]TTAGCATTCAACACT	54813
rs574847046	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942066	GCTGTGCACTCATAT[C/T]CAGCTACCATAGAAT	54813
rs574848662	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44951147	TTCTATTCTGTAGCT[C/G]TATTCTAAGGGTGTG	54813
rs574884316	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44940094	GATGGAAGACATCAC[A/G]TGAAGTGCAAGCGAG	54813
rs574985011	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44965303	CAGACAGCCTGTATT[G/T]AAATTTCCCAAATTG	54813
rs574986841	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44949739	ATAGCAGATTCCAAA[A/C]CAACTACCCAAGTAT	54813
rs575063328	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958572	TCAGTGAGCCTATGG[A/G]ATAAGTTAGGATATT	54813
rs575076407	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44959639	CCCTTAAGTTCAGCT[A/T]AAAAAATTAACATAT	54813
rs575079877	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44953301	CAACAGGATAAATTA[C/G]AAATGAATCAGAGGT	54813
rs575270324	snp	C/T	8.24504e-05	0.00642016	missense	KLHL28	GRCh38.p7	14:44945578	TTTCAGGACAAGTTT[C/T]ATCTGGAGTAGGTTT	54813
rs575270621	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954742	AAGGTAGATATTTTT[G/T]AATATACTCTGTTTT	54813
rs575358514	snp	A/C	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44968420	ACCCGCCACCATGCC[A/C]AGTATTTTTAGTAGA	54813
rs575370322	snp	A/C	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44955733	CGAGGCTGCAGTGTG[A/C]AGTGATTGCACAACT	54813
rs575371063	snp	C/T	0.0023933	0.0345097	intron-variant	FAM179B	GRCh38.p7	14:44968926	TTCCCTCTCTCACCC[C/T]ATTCCCAAGCCTTAG	54813
rs575524578	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961040	CTCCAAAGCATTCAG[C/G]CTCACACTAGACACT	54813
rs575529981	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962073	TCTTCCAGGAGACTT[G/T]GGCCTAGTCTCAACA	54813
rs575568809	snp	A/T	1.65151e-05	0.00287355	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963704	TTCGCCTTGGAGAGC[A/T]GGTACAGCAGTTCTT	54813
rs575725691	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44969009	ACATACTTGGAGTTA[C/T]ACAGTAGCTTGCATT	54813
rs575767736	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959790	TTCTGAGGTGTACTA[C/T]TAATAAAACACCTAA	54813
rs575885120	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44936419	AATCTAGTGAATAAG[C/T]AGAGAGGTGGAAGGG	54813
rs575910804	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925380	AGTTTTCTTACTAGA[A/G]AATACATTATCCAAT	54813
rs575948067	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924513	GCTAAAAAGGTACAT[A/G]TTCAGAGGTAAAATA	54813
rs575961591	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977426	TATTTTTAGTAAAGA[C/T]GGGGTTTCACCGTGT	54813
rs576125461	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967364	ACAGTAACCCCCCTC[C/T]CCCCACAAAATTGCT	54813
rs576231494	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960336	ACAAGAAAGAGTGCA[C/T]TGGATTTTCAACTTG	54813
rs576247376	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44950403	AGATTCATTTTTAAT[A/G]TAATTAGGAATCACA	54813
rs576304105	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44934676	CACAATAAACCATGA[C/G]ACACCTTCCAAAGTG	54813
rs576327585	in-del	-/CT	0.00517822	0.0506191	intron-variant	KLHL28	GRCh38.p7	14:44942296	AATCCTGTCAATTTA[-/CT]CTGTTAAAACATTTT	54813
rs576338997	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937215	CAGTGGCGCAATCTC[A/G]GCTCACCACAACCTC	54813
rs576391930	snp	A/C			synonymous-codon	KLHL28	GRCh38.p7	14:44945317	ATCATACTTGATCCA[A/C]GACTCTAATGCATAA	54813
rs576410425	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44968032	CAAAGCAAAAAGAAT[A/C]TGAAGATAAGTGCAT	54813
rs576410511	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44952154	TGTGAGCCACTGAGC[A/G]TGACCAAATTAAATC	54813
rs576584249	snp	A/T	0.0267878	0.112589	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928692	GCTAAAATAAAAAAA[A/T]AAAAAAAAAAAAAGC	54813
rs576591053	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955680	AGTCTCAGCTACTTG[C/G]GGGGCTGAGCTAGGA	54813
rs576627822	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927677	AAAAGATCATTTCTT[C/T]AATCAAAGTAGAACT	54813
rs576655324	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936560	TGTTTTTAAGAGAGC[A/C]GAAGGTGTCAGACAT	54813
rs576666378	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944437	CTGTTTGGTCTTTTA[C/T]AGAAAAAGTCTGACA	54813
rs576714656	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940503	TATGACTCCTTATGT[A/G]TAAGTAGAAACAATA	54813
rs576769837	snp	A/G			missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964384	TTAAGTGCAGGAAAA[A/G]GAAAAAATAAATTAC	54813
rs577009111	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978888	CCTGTAGTCTCAGCT[C/T]CTCAGGAGGCTGAGA	54813
rs577049976	snp	A/G	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44947880	GAAAAATTCTCAAAT[A/G]TTATTGCAGTCATGG	54813
rs577273476	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958398	AGATTACTCTTAAAA[A/T]AAAAATTCAAACCGA	54813
rs577381054	snp	G/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44971582	TTTTATTTTTCTCCT[G/T]CTCACTTTGGATTTA	54813
rs577440229	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950316	AAACCCACTCTGTCT[C/T]CTCTGATACCCTGGG	54813
rs577457573	in-del	-/TCT	0.00161322	0.028355	cds-indel, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964204	GCAGTACTGATGCCA[-/TCT]TCTGCCGGGGGTAGG	54813
rs577489855	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44964608	TCCATCTGAATGTTG[A/G]TACTCATTATAATGG	54813
rs577505490	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44965076	AGGTAAGAGTACAAT[A/G]AATACCCATATACTT	54813
rs577511644	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924468	AAATGACACTTTAGT[A/G]TGTAAACATAAATAA	54813
rs577689605	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44944708	AAATCTCTTCTGATG[C/T]GGTCTGACTCAAATA	54813
rs577717513	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961326	GAGGTTAGGGGAGAG[C/T]CCCACAGAGGAACTG	54813
rs577740476	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968384	CCTGCCTCAGCCTTC[C/T]GAGTAGCTGGGACTA	54813
rs577744435	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974799	TAATACAACATTCCT[C/G]CCATATCTGATGCTG	54813
rs577946799	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969744	GTGTCAGGTCTGTTT[C/G]TAGATTCATTTTTTT	54813
rs577951089	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927553	AATAATAAAATGCAA[A/G]TGAATGTGTTTAAGA	54813
rs577981733	snp	A/C	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44976708	TTAGCTACCAGTCAT[A/C]ATGTGTATAGTCAAT	54813
rs578066835	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970427	AATCATTTATTATTC[A/G]CAGGAGGATTTTTTT	54813
rs578098294	snp	C/T	1.65018e-05	0.00287239	missense, intron-variant	KLHL28	GRCh38.p7	14:44931431	ACTCCATTATGTCCA[C/T]CCACCACAAAAATAA	54813
rs745349710	snp	A/G	1.64885e-05	0.00287123	synonymous-codon	KLHL28	GRCh38.p7	14:44945833	GATGTCACAGAGTTC[A/G]TGATGTTGGCGAAGA	54813
rs745372336	snp	C/T	4.94434e-05	0.00497184	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964320	CCACGTGAGGGATAG[C/T]ATGCACATTTATGGA	54813
rs745390029	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44944475	ATCTAAGTTATTGGG[C/G]GGAAAAACATATTTC	54813
rs745403290	snp	C/T	1.65094e-05	0.00287305	missense	KLHL28	GRCh38.p7	14:44934466	ATAACATATACTTTT[C/T]GGTCTAAAACGCATA	54813
rs745417388	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961056	CTCACACTAGACACT[C/G]CAGCTCTTCCACTGT	54813
rs745478112	snp	C/G	1.65045e-05	0.00287263	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963259	ACAGCTTTCTCCGCA[C/G]TTCAACAAATTGGGG	54813
rs745548982	snp	A/G	1.75026e-05	0.0029582	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964431	ACCTGGAATCATGGG[A/G]GAAAACCAGACCTCC	54813
rs745560761	snp	C/T	1.64749e-05	0.00287005	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963122	GACTTAGAGCTTCCA[C/T]AGCACTACTGCTTCC	54813
rs745649999	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962347	GGCTTGGAGAGGATC[C/T]GGAAGTCTGGGCTCC	54813
rs745667658	snp	A/G	6.63526e-05	0.0057595	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963646	GACGATTCTAACTTC[A/G]AAGTGGTGCATGGCA	54813
rs745671618	snp	A/T	4.49873e-05	0.00474253	intron-variant	KLHL28	GRCh38.p7	14:44931285	TGCAAGCACATCATT[A/T]TAGAAAACATTGCCT	54813
rs745746906	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44934720	AGTCAGATAATAATT[A/G]TTGGCAAGAATGTGT	54813
rs745751842	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44969937	CATTGTCTTGATTAC[G/T]GTAGCTTTATAGTAA	54813
rs745780927	snp	A/G	1.64836e-05	0.0028708	missense	KLHL28	GRCh38.p7	14:44934364	TCTAGAGAAGTCCAA[A/G]TATTTGTATCAGGAT	54813
rs745797018	snp	A/G	1.68428e-05	0.00290192	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962518	CCTTCCGCCCCAGAG[A/G]CCGATGATAGTCGAG	54813
rs745838582	in-del	-/T			intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937313	CCACCCTCAGCTAAC[-/T]TTTTTTTGTATTTTT	54813
rs745908992	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926326	GCTCCTACTACTACT[A/G]CCCAAGATATTTCAC	54813
rs745918920	snp	C/G	5.11234e-05	0.0050556	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962774	TCCAGGCTTTGCAAG[C/G]TGCTTTGCCGCGGCG	54813
rs745924101	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44979389	TGTGTCCTTATGGGG[-/T]GGAAGGGACAAACAA	54813
rs745951285	snp	A/G	0.000182317	0.00954595	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962691	TGGAGGCGGTTTGTC[A/G]GGGGGAGATGAAGAG	54813
rs745959342	snp	C/T	1.64743e-05	0.00287	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964007	GCAGGGTACGCCAAG[C/T]AGCTTTAGAAGCTTT	54813
rs746029461	in-del	-/TGTACCCG	1.64976e-05	0.00287202	frameshift-variant, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964354	TACAGCCCAACTATC[-/TGTACCCG]AAGGGTATTAAGTGC	54813
rs746031640	snp	A/T			synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964203	TGCAGTACTGATGCC[A/T]TCTTCTGCCGGGGGT	54813
rs746234367	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44970482	GCAGACAATCATGTC[A/T]TCTGTGAACAAAGAC	54813
rs746235017	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44932945	CAGTCAACAAACCTC[A/C]GTATTTGTAGAGGAT	54813
rs746236810	snp	A/G	3.29603e-05	0.00405944	synonymous-codon	KLHL28	GRCh38.p7	14:44945674	CACAATGGCCTGGAG[A/G]GCAGTTTCATCAATG	54813
rs746261824	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44969388	GAACTCCCGGACTCA[A/C]GCGATTGCCCACCTT	54813
rs746283046	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44958174	CCATTTGAAATTAAA[A/C]TTAAAATAAAACTTT	54813
rs746283526	in-del	-/T			downstream-variant-500B	KLHL28	GRCh38.p7	14:44923872	TTGGCCTATGACATA[-/T]TTTCTTTTTTTTTTT	54813
rs746313441	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44955108	ATCTAGGATTCTTGG[C/T]ATGGGAAAAAGAAGG	54813
rs746331182	snp	C/T	2.75107e-05	0.00370872	intron-variant	KLHL28	GRCh38.p7	14:44931587	AGATCTTTTGTGTCA[C/T]TCTTCCTGTCAAAGC	54813
rs746338277	snp	C/T	1.64836e-05	0.0028708	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963878	ATAAGCATTCCAGAG[C/T]GAGAGAGGAGGTGGT	54813
rs746446879	snp	A/G	4.95037e-05	0.00497488	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931466	TAGCATGACACCCAC[A/G]CCAAAGTGAATCCTT	54813
rs746496272	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958722	TCTGAATCCATGTTA[C/T]GACAGGCGTCTAAGT	54813
rs746549785	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44956945	TCCTCAGCCTCCCAA[C/G]TAGCTAGAACTACAG	54813
rs746557479	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44973600	TCTCTCTCTCTCTAT[A/G]TATACATATATATAT	54813
rs746641436	snp	C/T	6.60229e-05	0.00574518	synonymous-codon	KLHL28	GRCh38.p7	14:44945860	AAGAAGATTCAAGCC[C/T]TGCAGAAGTTGTTCA	54813
rs746731614	snp	G/T	1.64803e-05	0.00287052	missense	KLHL28	GRCh38.p7	14:44945684	TGGAGAGCAGTTTCA[G/T]CAATGCATTGAAACT	54813
rs746746369	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44950458	CCTAATTTTTGTGTA[A/C]CCAATTCAAAACTGG	54813
rs746767032	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44935165	AACAAACTATAGCTA[C/G]ATGTCGCTGGGGGAA	54813
rs746809387	snp	A/G	1.67565e-05	0.00289447	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962527	CCAGAGACCGATGAT[A/G]GTCGAGTTGGGGGCA	54813
rs746839164	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44949072	TGTAAATTCATCTCT[C/G]TCTCAGACTAAACAA	54813
rs746858974	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44972178	AAATGAGATTTGGGA[C/T]AGGATACAAACCCAA	54813
rs746929077	snp	C/G	5.5436e-05	0.0052645	intron-variant	FAM179B	GRCh38.p7	14:44964473	TATAGAGCAGGTATG[C/G]TTCTCTAATTTTCTT	54813
rs746938313	in-del	-/G	5.01634e-05	0.00500791	upstream-variant-2KB, frameshift-variant, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962536	GATGATAGTCGAGTT[-/G]GGGGCATTATGAGAG	54813
rs746975155	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44936686	GTTTCTCCAGTTACA[C/T]TCTGCTGCTCAGATG	54813
rs747006829	snp	C/T	1.65726e-05	0.00287855	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962630	CGCCTCTGGCCTCGG[C/T]CCTCTTGATGCCCTC	54813
rs747053138	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44975211	AAACATCCAATAACT[A/G]CATTATACTGGAATG	54813
rs747064974	snp	G/T	1.64855e-05	0.00287097	missense	KLHL28	GRCh38.p7	14:44945205	CATCACGAATAAGAT[G/T]ATTTGCTTCATATAG	54813
rs747092316	snp	C/T	1.64866e-05	0.00287106	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962971	GCACTTTTGCCTCAA[C/T]TAGTTGTCTCGTTAC	54813
rs747195620	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44976136	CCGATAACACTCACT[G/T]TGATTAACATCTTTC	54813
rs747315864	snp	A/G	4.94458e-05	0.00497197	synonymous-codon	KLHL28	GRCh38.p7	14:44945347	AAAAACAGTCTCTTC[A/G]GTAGCTACATTCAAA	54813
rs747341214	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44929574	AGGAAAAAATATTAC[A/C]TATATAGGGTTTGGT	54813
rs747361939	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44968035	AGCAAAAAGAATCTG[A/C]AGATAAGTGCATTTC	54813
rs747373495	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44931128	AAACAATAATATGCA[C/T]ATTGGCATATAAAAG	54813
rs747401424	snp	C/T			synonymous-codon	KLHL28	GRCh38.p7	14:44945692	AGTTTCATCAATGCA[C/T]TGAAACTCAACCTCA	54813
rs747405282	snp	A/G	1.64958e-05	0.00287187	intron-variant	KLHL28	GRCh38.p7	14:44934075	AATGAGACTTTTAAA[A/G]ATCCATAAACATATG	54813
rs747430781	snp	C/G	1.88945e-05	0.00307358	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962387	TTTGGAGACGGCAAT[C/G]GTTTCTTCCAACCAC	54813
rs747449885	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44969284	AGGCTCCCAAGTAGC[A/T]GAGACTACAGGCCCA	54813
rs747472678	snp	C/G/T	8.23722e-05	0.00641717	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964151	GATTGGCTAGGAAAA[C/G/T]CTTACCAAGGCTCAC	54813
rs747643180	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44971984	AAAGTGAAGAGGAAG[G/T]AGTCACGTCTTACAT	54813
rs747666455	snp	G/T	1.65165e-05	0.00287367	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963477	ATTTGGGATTATTCC[G/T]CAGGAGCTGCATTCA	54813
rs747710773	snp	A/C	1.64762e-05	0.00287016	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964060	GGCTCAGGTAAAACC[A/C]GCATCCTTTTTAAAG	54813
rs747715140	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44971026	TTTTTGTTTTTTTTC[C/T]TATAAGGTCTTTGCT	54813
rs747721007	snp	A/C	1.64827e-05	0.00287073	missense	KLHL28	GRCh38.p7	14:44934226	ACAGGTTGCCATTTT[A/C]TTATTTTGGGAATGT	54813
rs747730550	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44956437	TAACACCCATGAGTA[C/T]TCTCACGTCCCAACC	54813
rs747821496	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940858	TAATTATAAAAATAC[C/T]TGGGAGGCTGAGGCG	54813
rs747983176	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44965869	GCTTACAAATAGTAA[-/T]TTTTTTTTTTTTTTT	54813
rs748145702	snp	C/G	1.64838e-05	0.00287083	missense	KLHL28	GRCh38.p7	14:44945175	CTTCATTCAAAAGAT[C/G]TTTACAAGTGCGATC	54813
rs748179491	snp	C/T	2.18965e-05	0.00330874	intron-variant	KLHL28	GRCh38.p7	14:44931300	ATAGAAAACATTGCC[C/T]TACATGTTTAGAAAT	54813
rs748265606	snp	A/G	1.64866e-05	0.00287106	missense	KLHL28	GRCh38.p7	14:44945490	GGTCACGGCAACCAT[A/G]TGTTTCTGCAAAACG	54813
rs748267673	snp	C/G	1.64936e-05	0.00287168	missense, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929097	CAGCCACGTATCTGA[C/G]ATAGGATCATATTTC	54813
rs748317794	snp	G/T	1.65048e-05	0.00287265	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963756	TGTCAAAGTGCTGGC[G/T]GACAACAAGTTGGTG	54813
rs748332981	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44974123	TCTTTTCTATATTCT[C/G]TTCCTAGTAATCCCA	54813
rs748378899	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44948044	TGTTGATCTTTTTAA[-/C]CTATGTAACTTCTTT	54813
rs748405799	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44938457	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	54813
rs748427902	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44938708	GTGAATAATCTCCTT[C/T]GACTCCATGTCCTAC	54813
rs748556420	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964161	GAAAACCTTACCAAG[A/G]CTCACAGAGCAGGGA	54813
rs748581640	snp	A/C	3.29478e-05	0.00405867	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963109	AGTACCGATGCCCGA[A/C]TTAGAGCTTCCACAG	54813
rs748603133	in-del	-/AACTTCTTGTT	1.64882e-05	0.00287121	frameshift-variant	KLHL28	GRCh38.p7	14:44934185	CCGCTGCAGCAAAAC[-/AACTTCTTGTT]GTCGTCATTGGTGCC	54813
rs748604955	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44979217	AAGGCAGCTATTCTT[C/T]TTCCTGCTGCTGTAA	54813
rs748631961	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44965649	TGATATCAGGCTGTC[A/C]CATCACTGGTGATGC	54813
rs748643447	snp	A/G	1.64811e-05	0.00287059	missense	KLHL28	GRCh38.p7	14:44945360	TCGGTAGCTACATTC[A/G]AACAGTCATTGGAAA	54813
rs748669576	snp	A/T	1.64825e-05	0.00287071	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964282	GGTAACAGAACTCAG[A/T]GTGCACACTGTCACT	54813
rs748752533	snp	A/G	1.64789e-05	0.0028704	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962991	TGTCTCGTTACGGGA[A/G]GAGAATCCAGCCCTG	54813
rs748760708	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44929331	TACAGGCAATATACA[G/T]TAGTCCTCCCTTTAT	54813
rs748809950	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44933123	AATAGCTGTTATACT[A/G]TATTATTTTGTTTTT	54813
rs748815421	snp	C/G	1.85317e-05	0.00304393	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962445	TGCCCCCTCCGCGCT[C/G]CTTCTGCTGCCGCCC	54813
rs748835176	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44970658	TTCTCATAAATATGA[G/T]GTTATCTGTATGCTT	54813
rs748838457	snp	C/T	0.000115375	0.00759437	synonymous-codon	KLHL28	GRCh38.p7	14:44934249	GGGAATGTACTTCTC[C/T]ACAGATTGTAAATAA	54813
rs748889134	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44967727	GATGTAGATGGGGTA[A/G]AGTATGGAGATAATA	54813
rs748889964	snp	C/T	1.64811e-05	0.00287059	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964306	TGTCACTGTGGTGAC[C/T]ACGTGAGGGATAGCA	54813
rs748960149	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44934897	TTATAATTTTGCATC[A/T]AGATAAATATACACA	54813
rs748977753	snp	A/G/T	0.000131789	0.00811666	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964192	TTTGTGGAATATGCA[A/G/T]TACTGATGCCATCTT	54813
rs749009458	snp	G/T	1.64819e-05	0.00287066	missense	KLHL28	GRCh38.p7	14:44934323	GTACTACTACTCCAA[G/T]AGTACTTCGGCTTTC	54813
rs749034848	snp	A/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924480	AGTGTGTAAACATAA[A/T]TAAAATAAAACCCTG	54813
rs749070139	snp	A/T	1.6483e-05	0.00287076	synonymous-codon	KLHL28	GRCh38.p7	14:44945326	GATCCAAGACTCTAA[A/T]GCATAAAAAACAGTC	54813
rs749079949	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44975863	GGTATTAGGACAACT[C/G]CCTTGTTAACAATAT	54813
rs749082021	snp	G/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961208	CCAAGAACTTCCACC[G/T]CAAGTGAAATTGTCT	54813
rs749087368	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44939717	TCTATCAACATTCTG[A/C]TCATGCCCACTTAAG	54813
rs749137134	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44975161	TCCCCTTTCTGTGTA[C/T]GTTTTCATTAGCCAC	54813
rs749169647	snp	A/C			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962257	CGGGGGCCATTTTGC[A/C]AGAGGCTGCCTCCCG	54813
rs749202663	snp	A/G	1.6607e-05	0.00288153	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963618	CTTCATTAGTTTGCT[A/G]TATAATTTGTTAGAC	54813
rs749239411	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44940355	CAATAATAATCAGTT[A/C]TAATAAGAGTTTCAT	54813
rs749240541	in-del	-/CA			intron-variant	KLHL28	GRCh38.p7	14:44946230	CTTTACCAACTTTTT[-/CA]TTTTGTTTCCCCTGC	54813
rs749279838	snp	A/G	1.65312e-05	0.00287495	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963501	GCATTCACGATTATT[A/G]GATCAGGAAGACTAT	54813
rs749332876	in-del	-/ACC	1.88702e-05	0.00307161	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962397	CAATGGTTTCTTCCA[-/ACC]ACCACCACCACCTGA	54813
rs749340329	snp	A/G	1.65023e-05	0.00287244	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963779	AGTTGGTGATCAAAC[A/G]AGAATACATGAAAAT	54813
rs749358499	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44965513	CAAGTTTTACATTTA[C/T]ATGTTTACTTGATTA	54813
rs749402319	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958558	GGTATATAATTCTAT[C/T]AGTGAGCCTATGGAA	54813
rs749413421	snp	A/G	1.64999e-05	0.00287222	missense, intron-variant	KLHL28	GRCh38.p7	14:44931441	GTCCACCCACCACAA[A/G]AATAAAGCCTAGCAT	54813
rs749413570	snp	G/T			missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964421	AAAATGAGCAACCTG[G/T]AATCATGGGAGAAAA	54813
rs749452622	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44950722	AAAAAATAGACAAAA[C/T]TGTATAAAAAGCAGT	54813
rs749527486	in-del	-/GCCCCA	1.6476e-05	0.00287014	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963967	CTGTCCTTTGATCTT[-/GCCCCA]GCTCTTGTAGATAGC	54813
rs749575075	snp	A/G	0.000149891	0.00865582	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962549	TTGGGGGCATTATGA[A/G]AGGAGAGAAAAACTA	54813
rs749582944	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44979031	AATAGAAATAACAGA[-/T]AAAAAAAAAAGGTTA	54813
rs749589830	snp	C/T	1.64819e-05	0.00287066	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963856	TTACTCCTGGAACAT[C/T]TCAAACATAAGCATT	54813
rs749637128	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44941300	CACTTCTAGGCCCAC[C/T]GTAATGTATCTACAG	54813
rs749739526	snp	A/T	1.64822e-05	0.00287068	missense	KLHL28	GRCh38.p7	14:44945631	CTGTGTCCTGAGAAA[A/T]AAAAACAGTCCCTGT	54813
rs749758466	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44977336	ACCTTCCGGGTTCAC[A/G]CCATTCTCCTGCCTC	54813
rs749828747	snp	C/G	1.64933e-05	0.00287165	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963241	ACAGAAGAAGAATCT[C/G]AGACAGCTTTCTCCG	54813
rs749838883	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925546	AGGAATTAGATTCAT[C/T]CTTCACCAAAATAGT	54813
rs749860556	snp	C/T	1.64885e-05	0.00287123	missense	KLHL28	GRCh38.p7	14:44945517	AACGAGAAATTCCAA[C/T]ACAATTACCAGGATC	54813
rs749867845	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942600	AAGACCACTGCTTGA[C/T]ACTTCTTGGTTAGAA	54813
rs749894595	snp	A/G	2.53733e-05	0.00356174	intron-variant	KLHL28	GRCh38.p7	14:44934597	TAAAATTTAAAAACC[A/G]AAGTGGCCCATAAAG	54813
rs749903803	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44975071	TGCTTCCTTTACCCC[-/T]CTCTGTGTATATTTT	54813
rs749914627	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940732	CACAACTTTCTATCA[C/T]TGCTTTTGATATCAA	54813
rs749977114	snp	C/T	1.64855e-05	0.00287097	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963916	TGCATCTGCTCCCTG[C/T]TGACCTATCCTAGTG	54813
rs749984546	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44975595	CCTCAGCCTCCCGGA[C/T]AACTGGGATTACAGG	54813
rs750069865	in-del	-/GG			intron-variant	KLHL28	GRCh38.p7	14:44950172	GTTTATACATAAAAA[-/GG]GCTCAGAATAGGGCC	54813
rs750078208	in-del	-/TTT			intron-variant	KLHL28	GRCh38.p7	14:44942866	AAACATTATGTATTA[-/TTT]TCTACATGTCTCCTT	54813
rs750094685	snp	G/T	1.64822e-05	0.00287068	missense	KLHL28	GRCh38.p7	14:44945157	TAAAGTGGTACTTTA[G/T]GGCTTCATTCAAAAG	54813
rs750156929	snp	C/G	1.66065e-05	0.00288149	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963603	TTCTAGTCTTGTTGG[C/G]TTCATTAGTTTGCTA	54813
rs750164721	snp	A/G	1.65141e-05	0.00287346	missense, intron-variant	KLHL28	GRCh38.p7	14:44931413	ATGCTGGACAAATGT[A/G]AGACTCCATTATGTC	54813
rs750279861	in-del	-/AAT			intron-variant	FAM179B	GRCh38.p7	14:44966476	AGACTGCATCTCAAA[-/AAT]AATAATAATACTAAA	54813
rs750300347	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924845	AATATAAAAGACATA[C/T]GGATAACAATTTTTC	54813
rs750312575	snp	A/C	1.75038e-05	0.00295831	splice-acceptor-variant, intron-variant	KLHL28	GRCh38.p7	14:44931542	TCATAACGCTCCACA[A/C]TGCAAATATTTAAAA	54813
rs750347576	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44972181	TGAGATTTGGGACAG[A/G]ATACAAACCCAAACC	54813
rs750402666	snp	C/T	3.2963e-05	0.00405961	synonymous-codon	KLHL28	GRCh38.p7	14:44934267	AGATTGTAAATAAGA[C/T]TGTCCATCATAACCA	54813
rs750507664	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44942101	TTTACCTGGATATTT[C/G]ATAGGCACTTCAAAC	54813
rs750522885	snp	C/T	3.74693e-05	0.00432819	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962430	ACCCTGCATGGCGGC[C/T]GCCCCCTCCGCGCTG	54813
rs750554895	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44956036	TAGCAACTCATTTTT[G/T]GAAACCTAGTAAACA	54813
rs750588717	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44977704	AGTGCAGTCGTATGA[A/G]CTGCACTTGCAGCTC	54813
rs750592218	snp	G/T	1.64904e-05	0.00287139	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962964	TAGCTTAGCACTTTT[G/T]CCTCAACTAGTTGTC	54813
rs750735432	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44934664	AAAAATTAAAAGCAC[A/C]ATAAACCATGACACA	54813
rs750738929	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44943371	ACAGTTAAAATGTAT[C/T]ATGAGGCTGGGTGCA	54813
rs750744839	snp	A/G	3.2981e-05	0.00406071	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964145	AGGCCAGATTGGCTA[A/G]GAAAACCTTACCAAG	54813
rs750769662	snp	A/T	1.66021e-05	0.0028811	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928990	TGTTCATGCAGTACA[A/T]GTTTCACCACCATAC	54813
rs750830095	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44971723	GCTTTCACTGCATAC[C/T]GCAAATCTTGATACA	54813
rs750900547	snp	A/C	0.000120547	0.00776267	utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44960967	CTTAGACTTTTCGCA[A/C]GAGTCATTCAAAAGT	54813
rs750944430	snp	A/C			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927895	TAACTTTCTTTAAAT[A/C]ACTATTCAGGAACCA	54813
rs750961010	snp	A/C			utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961105	TATGAGGAGAAAATG[A/C]ACACAAAATTCTCAG	54813
rs750970287	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44935774	CAGAAGTATTGTTAA[C/T]AGTCTGTGAAGCTGG	54813
rs750979043	snp	C/T			synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964143	GCAGGCCAGATTGGC[C/T]AGGAAAACCTTACCA	54813
rs751012980	snp	A/T	1.64838e-05	0.00287083	missense	KLHL28	GRCh38.p7	14:44945284	TAACTGTGCTAAGTA[A/T]TTCTGGCGTTCTTGT	54813
rs751148764	snp	G/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44960946	ATTTGGGTCTTCAAA[G/T]GATAACTTAGACTTT	54813
rs751194424	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44946255	CCCCTGCATTAAATT[A/C]AAGTCTGAGCTATCA	54813
rs751245222	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44979254	GTCTTAGACTGGGTA[A/C]TTTATAAACAATAGA	54813
rs751297128	snp	A/G			downstream-variant-500B	KLHL28	GRCh38.p7	14:44923971	GCCTCCCAGGTTCAA[A/G]CGATTCCCCTGCCTC	54813
rs751323405	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928950	CAATGCAGCTTGTGG[A/G]TTTCAGAAAACTGGG	54813
rs751336217	snp	A/T	1.65778e-05	0.002879	missense	KLHL28	GRCh38.p7	14:44934154	CCACCAATGGCATAT[A/T]TCATTCCATCCAATA	54813
rs751336826	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44967007	CCTAGCCTTACTTTG[G/T]TTTTTTTTTTCTTGC	54813
rs751356950	snp	C/T	1.64838e-05	0.00287083	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963847	GTGCTTTGTTTACTC[C/T]TGGAACATCTCAAAC	54813
rs751387750	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44978989	TTTTTTTTTTTAATG[A/T]CACTAACCAATCCTA	54813
rs751391719	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44965161	CCATTTGAAAGTAAA[C/T]TGTGGATATCTTGAG	54813
rs751463431	snp	A/C	0.000117484	0.00766344	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962735	TTCAACTCCTCCGCA[A/C]TGCCCGGGATCCTTC	54813
rs751647943	snp	C/T			missense	KLHL28	GRCh38.p7	14:44934469	ACATATACTTTTTGG[C/T]CTAAAACGCATATTC	54813
rs751684670	snp	A/G/T	6.59321e-05	0.0057413	synonymous-codon	KLHL28	GRCh38.p7	14:44934420	TTTTCTGATAGTGAC[A/G/T]CCAGGACGCACATTA	54813
rs751688504	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44969435	GGGATTACAGGTGCA[A/T]GCTACCACGCCTGGC	54813
rs751690173	snp	A/G	1.64814e-05	0.00287061	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964253	ATGGAGCAGATACGG[A/G]CTGGCTTTTGGCTGG	54813
rs751698150	snp	C/T	1.64944e-05	0.00287175	missense	KLHL28	GRCh38.p7	14:44945480	GCCAAATAAAGGTCA[C/T]GGCAACCATATGTTT	54813
rs751783985	snp	C/T	1.65037e-05	0.00287256	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964358	GCCCAACTATCTGTA[C/T]CCGAAGGGTATTAAG	54813
rs751796645	snp	C/T	1.64757e-05	0.00287012	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963182	TTGGTCTGGATCTCA[C/T]CGAGGTGATAATATC	54813
rs751799868	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44955908	AGACAGGACAAACTG[A/G]TCATCAATAATAATA	54813
rs751896711	snp	A/C	1.65968e-05	0.00288065	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963578	AATTTAACCCTAGTT[A/C]TACTCCTCATTCTAG	54813
rs751897037	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44946951	AAATAGCAGGGAAGA[A/G]AAGGGATGAGAAAGA	54813
rs752033792	in-del	-/A	1.94687e-05	0.00311993	intron-variant	KLHL28	GRCh38.p7	14:44931554	ACACTGCAAATATTT[-/A]AAAAAAATTTAATTT	54813
rs752046392	in-del	-/TT	3.3024e-05	0.00406336	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963303	AGACAGGTTTCAATC[-/TT]ACATTTCTCGTCTGC	54813
rs752054910	snp	C/T	4.9445e-05	0.00497193	missense	KLHL28	GRCh38.p7	14:44934292	TAACCACCTAAGGCA[C/T]AAAGTTCTCCTGCAA	54813
rs752068518	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44932705	ATCATTGAAGAAGAG[C/T]TGATGCACTGCAGCA	54813
rs752124595	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44948074	TTAGCCTCAGTTTTA[C/T]GAAAAAGTTAAAATC	54813
rs752130446	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44957748	CAGAGAAATTAAGTC[C/T]AAGGCAAGATTTAAA	54813
rs752138844	snp	A/G	3.30753e-05	0.00406652	synonymous-codon, stop-gained	KLHL28	GRCh38.p7	14:44929172	ATAAAGGTAGTTATC[A/G]ATTACAGCAGCACCA	54813
rs752158438	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44966499	TAATACTAAAATAAA[C/T]TAATTACAAAAAGAG	54813
rs752174615	snp	A/C	1.65165e-05	0.00287367	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929016	CATACTATTTCCGAG[A/C]GTTCACATTTGTCAA	54813
rs752208755	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44936357	GATATAGGAGAGAGA[C/T]AGGATAAATGGAAAA	54813
rs752229133	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44951353	AGCCACGGATAAGCT[A/G]CAGTCCTGAGGTCCA	54813
rs752279776	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44973573	TTATTCTCCTCCAGT[G/T]TACTTTCTCTCTCTC	54813
rs752361212	snp	C/T	1.86499e-05	0.00305362	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962436	CATGGCGGCTGCCCC[C/T]TCCGCGCTGCTTCTG	54813
rs752376719	snp	G/T	1.65261e-05	0.0028745	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963692	ATTTACTGGTTATTC[G/T]CCTTGGAGAGCAGGT	54813
rs752454017	snp	G/T	1.6607e-05	0.00288153	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963602	ATTCTAGTCTTGTTG[G/T]CTTCATTAGTTTGCT	54813
rs752460574	snp	A/G			intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937684	AGAATACTACAGACT[A/G]GGTAATTTATAAAGA	54813
rs752462727	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44977143	TCTAACTCTTCATAT[G/T]CTGCTTTATATATAT	54813
rs752496427	snp	A/C/G	0.000134681	0.00820511	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962741	TCCTCCGCACTGCCC[A/C/G]GGATCCTTCTGAGGC	54813
rs752602750	snp	C/T	1.64822e-05	0.00287068	missense	KLHL28	GRCh38.p7	14:44945306	CGTTCTTGTACATCA[C/T]ACTTGATCCAAGACT	54813
rs752666498	snp	A/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928685	AAGGAGAGCTAAAAT[A/T]AAAAAAAAAAAAAAA	54813
rs752690770	snp	C/T	1.65031e-05	0.00287251	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962949	GCTTGAAGAGGCCTT[C/T]AGCTTAGCACTTTTG	54813
rs752697209	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44948903	TGCAATTAATTCAAT[A/T]ATACGTGTTGCTCTG	54813
rs752736825	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44930996	AAAACAGAACAATCC[A/G]AGGATTGTATGTATG	54813
rs752764778	snp	A/G	4.94629e-05	0.00497283	synonymous-codon	KLHL28	GRCh38.p7	14:44945604	GGTTTGCTGCTGGCA[A/G]GAGAGATTCAACTGT	54813
rs752784543	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44932632	CCATTCTGGAGTTCA[C/T]AATAGAGACTGGGTA	54813
rs752798834	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44968943	TTCCCAAGCCTTAGC[A/C]ACCAGTGGTCTTTTT	54813
rs752839578	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44946849	GCATGGGCCACCACA[C/G]CCGGCCTCAACTCTT	54813
rs752851971	snp	C/G/T	8.23771e-05	0.0064173	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963203	TGATAATATCCCTAG[C/G/T]CCGAAAGCTTGGTGA	54813
rs752902648	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44965135	GACATATTTCCTCCA[C/T]ATTTGCTGAACCATT	54813
rs752926631	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44970155	GCTTGACAATATTGA[A/G]TCTTCCTATCCACAA	54813
rs752960949	snp	C/T	1.648e-05	0.0028705	missense	KLHL28	GRCh38.p7	14:44945775	TGACGCTGGCAAGTA[C/T]CACTTTGTGAGCATG	54813
rs752983983	in-del	-/A	1.65132e-05	0.00287339	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963472	CTTAAATTTGGGATT[-/A]TTCCTCAGGAGCTGC	54813
rs753037195	snp	C/T	1.72448e-05	0.00293634	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962496	TCGGCTCCAGAGCCG[C/T]AGTCGTCCTTCCGCC	54813
rs753081205	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958486	ATCACATCTGCTCTT[C/T]TCTTAAATTTCTTTC	54813
rs753203524	in-del	-/A			intron-variant	FAM179B	GRCh38.p7	14:44976175	AACAATCTTCAAGAT[-/A]AAAATACAGAATTCA	54813
rs753214894	snp	C/T			missense	KLHL28	GRCh38.p7	14:44945255	CTCAACAATGGTAAT[C/T]GTACACTGTTTAGTA	54813
rs753223840	snp	A/T	3.37981e-05	0.0041107	stop-gained, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964397	AAGGAAAAAATAAAT[A/T]ACCATGGGAAAATGA	54813
rs753246136	snp	A/T	5.86677e-05	0.00541575	intron-variant	KLHL28	GRCh38.p7	14:44934567	CTCCACACTAAAGAA[A/T]AAGCAGAAAAAATAT	54813
rs753256922	snp	A/G			upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962000	CGTCACATCCGTCAA[A/G]TGGCTTCACCCCTCC	54813
rs753365483	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44964875	AGCAGTTAACAAATT[C/T]GTTAAGTGCTAAAGT	54813
rs753377475	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44948550	TTACCTGAAAGTGAT[G/T]CTCTAAAGTATAAAG	54813
rs753490616	in-del	-/AATAAAACCT			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925453	TTTCTTTTTCATGCC[-/AATAAAACCT]AATTGGACACTAAGG	54813
rs753510546	snp	G/T	1.66134e-05	0.00288208	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962573	AAAACTACTACTTCC[G/T]TGGAGCTGCGGGGGA	54813
rs753512662	snp	A/G	1.6492e-05	0.00287154	missense	KLHL28	GRCh38.p7	14:44934451	GTTGCAATACCACCT[A/G]TAACATATACTTTTT	54813
rs753584815	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940982	GCATATGCCTGTAAT[C/T]CCAGGTACTCAGGAG	54813
rs753614492	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44949695	TATCTAACAAGAAGA[A/C]ATTTAAAAGGGATAA	54813
rs753701888	snp	A/G	0.000164723	0.00907383	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963076	GTGCTGAGAACGCTT[A/G]TACAACAAGGACTGG	54813
rs753715553	snp	C/G	1.64893e-05	0.0028713	missense	KLHL28	GRCh38.p7	14:44945562	GAAATGCACAACATT[C/G]TTTCAGGACAAGTTT	54813
rs753718473	in-del	-/TT			intron-variant	KLHL28	GRCh38.p7	14:44954466	GCAACAAAAGAATGG[-/TT]GTGAAAACTATAGAG	54813
rs753727708	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44942818	TAAATGGTTCTCTTT[A/C]ATGTTTCTATAAAAC	54813
rs753740979	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44976919	ATTGGTTTACTAGCT[C/T]TCTACTTCTAAACCT	54813
rs753771942	snp	C/T	5.03664e-05	0.00501803	intron-variant	KLHL28	GRCh38.p7	14:44929217	TTGGCAAAAAGAAGA[C/T]AGAAACATGTTAACC	54813
rs753817183	snp	A/C			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926035	CTAATACTTTTAATC[A/C]TGAGGATTTATAACC	54813
rs753901142	snp	A/T	2.09875e-05	0.00323933	intron-variant	KLHL28	GRCh38.p7	14:44931562	AATATTTAAAAAAAA[A/T]TTAATTTACAGATCT	54813
rs753907485	snp	C/T			missense	KLHL28	GRCh38.p7	14:44945099	GGAGCACAGCGAGGT[C/T]GTGTCATCAAGACTG	54813
rs753943605	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44980210	TTTAACATTTACAGT[C/T]CACTGTTAATCTGTT	54813
rs753984118	snp	C/G	1.64751e-05	0.00287007	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963976	GATCTTGCCCCAGCT[C/G]TTGTAGATAGCAAAC	54813
rs753995653	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44967288	TATTTGAATCTCCCT[C/T]CGTTCACAATAAAAT	54813
rs753996147	snp	A/G			synonymous-codon	KLHL28	GRCh38.p7	14:44945791	CACTTTGTGAGCATG[A/G]ATTTTAACATCACCT	54813
rs754098393	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44943718	AATGTATTATCGGAC[-/T]TTTTTTTTTTTTTCA	54813
rs754129557	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44973435	TCATTTCATTTATAC[A/G]TAAACACACAGACAC	54813
rs754152977	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44930555	AGGTGTGAGCCACAC[C/T]GTGCCTGGCCCAACA	54813
rs754189474	snp	A/G	1.64811e-05	0.00287059	missense	KLHL28	GRCh38.p7	14:44945139	AGAGTCTATGTTCAG[A/G]CATAAAGTGGTACTT	54813
rs754243851	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44936211	GTAAAATAAATATGA[A/G]CAGATAGCTATGAAG	54813
rs754279350	snp	A/G	2.05375e-05	0.00320442	intron-variant	KLHL28	GRCh38.p7	14:44934573	ACTAAAGAATAAGCA[A/G]AAAAAATATAAAATT	54813
rs754322749	snp	C/T	1.65149e-05	0.00287353	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963320	ACATTTCTCGTCTGC[C/T]CTCTGCCCTGAGGAG	54813
rs754370733	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44958263	GCGAGTTTTGTACCT[A/G]TCTACTTAATTGACA	54813
rs754395939	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44933104	TTACTTATAATACTA[C/T]GCAAATAGCTGTTAT	54813
rs754397785	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44936002	TCCAGTATAATCAAG[C/T]TATATTCATTCACTC	54813
rs754436411	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44953205	TGCGAGGGAAAAGAG[A/T]AACGTTTAAATAAAT	54813
rs754456839	snp	A/G	1.6483e-05	0.00287076	missense	KLHL28	GRCh38.p7	14:44945292	CTAAGTATTTCTGGC[A/G]TTCTTGTACATCATA	54813
rs754499000	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44934945	AACACAATCATCCAC[C/T]AAAAGAATGGTTAAA	54813
rs754520018	snp	A/C	1.88763e-05	0.0030721	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962392	AGACGGCAATGGTTT[A/C]TTCCAACCACCACCA	54813
rs754577793	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44948677	CCATTCTTTCCCACA[A/G]TGACCTTTTACTCTT	54813
rs754590882	snp	A/T	1.65979e-05	0.00288074	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963587	CTAGTTCTACTCCTC[A/T]TTCTAGTCTTGTTGG	54813
rs754593103	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44971962	CGGAAATTTACAATT[A/G]TGGCAGAAAGTGAAG	54813
rs754605997	snp	C/T	1.65124e-05	0.00287331	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963470	ATCTTAAATTTGGGA[C/T]TATTCCTCAGGAGCT	54813
rs754758904	snp	C/T	1.65666e-05	0.00287802	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962644	GCCCTCTTGATGCCC[C/T]CGGAGGCAGTCTCAA	54813
rs754802851	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44973099	GGATTAATATCTACC[A/G]TAATTGTTGTTTTCT	54813
rs754818289	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44941014	CTGAGGCAGGAGAAT[C/T]GCTCGAACTCAGGAG	54813
rs754868440	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44976006	ATTTTTTTAAAATTA[C/T]GAGATATGGTAAAGA	54813
rs754884073	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44977134	TCAAATGCATCTAAC[G/T]CTTCATATTCTGCTT	54813
rs754899514	snp	A/G	1.64836e-05	0.0028708	synonymous-codon	KLHL28	GRCh38.p7	14:44945173	GGCTTCATTCAAAAG[A/G]TGTTTACAAGTGCGA	54813
rs754954026	snp	A/G	3.35993e-05	0.0040986	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962737	CAACTCCTCCGCACT[A/G]CCCGGGATCCTTCTG	54813
rs754979510	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962266	TTTTGCCAGAGGCTG[C/T]CTCCCGGAGTTGGGG	54813
rs754988848	in-del	-/CAAT			intron-variant	FAM179B	GRCh38.p7	14:44977887	ACTCCTGAGCTCAAG[-/CAAT]CCTCCCTCCACTGCC	54813
rs755083180	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44979154	TGTATCCCTAATTTG[C/T]TTACCTATAAGTCAC	54813
rs755101967	snp	A/T	1.64735e-05	0.00286993	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963101	GACTGGAAAGTACCG[A/T]TGCCCGACTTAGAGC	54813
rs755104435	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44930562	AGCCACACCGTGCCT[A/G]GCCCAACATCTGAAA	54813
rs755186414	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44968784	GATTTTGGCAAATGT[A/G]TCCATGTCTTATGTT	54813
rs755208312	snp	C/G	1.64914e-05	0.00287149	synonymous-codon	KLHL28	GRCh38.p7	14:44945584	GACAAGTTTTATCTG[C/G]AGTAGGTTTGCTGCT	54813
rs755300344	snp	A/G	1.64947e-05	0.00287177	missense	KLHL28	GRCh38.p7	14:44945481	CCAAATAAAGGTCAC[A/G]GCAACCATATGTTTC	54813
rs755302869	in-del	-/A	1.94687e-05	0.00311993	intron-variant	KLHL28	GRCh38.p7	14:44931553	ACACTGCAAATATTT[-/A]AAAAAAAATTTAATT	54813
rs755353871	snp	A/C/G	9.32382e-05	0.00682726	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962435	GCATGGCGGCTGCCC[A/C/G]CTCCGCGCTGCTTCT	54813
rs755355262	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44956397	GAGAGATAGCTAGAT[A/G]ATTGGGCCTTCTGAT	54813
rs755391540	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44973479	CATAATCAAATACAT[G/T]GTTGCTATTATTATT	54813
rs755455843	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44933133	ATACTGTATTATTTT[G/T]TTTTTTATTATTGTA	54813
rs755473157	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44943835	TCCTCTTGCCTCAGC[C/T]TCCTGATTAGCTGGG	54813
rs755512613	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958302	ACAAAACAGTGGTGC[C/T]GAAATCAGTTGGGAG	54813
rs755517468	snp	C/T	1.64822e-05	0.00287068	synonymous-codon	KLHL28	GRCh38.p7	14:44934303	GGCATAAAGTTCTCC[C/T]GCAAGTACTACTACT	54813
rs755623710	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44950352	CAAGTATCACAGAAT[G/T]GTTGATTCTCAAATC	54813
rs755636291	snp	A/T	1.66449e-05	0.00288482	intron-variant	KLHL28	GRCh38.p7	14:44929199	ACCAACTCCTAGGAA[A/T]GGTTGGCAAAAAGAA	54813
rs755659647	snp	C/G/T	3.29626e-05	0.00405961	missense	KLHL28	GRCh38.p7	14:44934317	CTGCAAGTACTACTA[C/G/T]TCCAAGAGTACTTCG	54813
rs755708259	snp	C/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962195	CGGTTTGGTCACGTG[C/G]TGCCCTTGGTTACGC	54813
rs755721874	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44933087	TTTAAATCATCTCTA[A/G]ATTACTTATAATACT	54813
rs755764381	snp	C/T	1.71311e-05	0.00292664	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962500	CTCCAGAGCCGCAGT[C/T]GTCCTTCCGCCCCAG	54813
rs755804197	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44947070	ATATTACTTTATATG[A/G]CAAAAAGGGACTTTG	54813
rs755855059	snp	A/G	1.65181e-05	0.00287381	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963697	CTGGTTATTCGCCTT[A/G]GAGAGCAGGTACAGC	54813
rs755856709	snp	A/C/T	3.72608e-05	0.00431616	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962439	GGCGGCTGCCCCCTC[A/C/T]GCGCTGCTTCTGCTG	54813
rs755857912	snp	A/G	1.64958e-05	0.00287187	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962955	AGAGGCCTTTAGCTT[A/G]GCACTTTTGCCTCAA	54813
rs755872461	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44970147	AACTAACAGCTTGAC[A/C]ATATTGAGTCTTCCT	54813
rs755902537	snp	A/G	1.64844e-05	0.00287087	synonymous-codon	KLHL28	GRCh38.p7	14:44945185	AAGATGTTTACAAGT[A/G]CGATCATCACGAATA	54813
rs755951578	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44952964	TTAATTTTAGAGTCG[A/G]ACAGATTTGGATTTA	54813
rs756037749	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44972407	TTATGATGTTGTTGA[A/G]TTCAACTGTGTCTTT	54813
rs756096774	snp	A/T	1.64819e-05	0.00287066	missense	KLHL28	GRCh38.p7	14:44945309	TCTTGTACATCATAC[A/T]TGATCCAAGACTCTA	54813
rs756134709	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927362	TATGTTTTATAATTA[C/T]AAATGGCTTCTTAAC	54813
rs756143926	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44975113	AAAGCAATAATTTTG[C/T]TCCAAATTGCTAAAT	54813
rs756246324	snp	A/G	1.64885e-05	0.00287123	synonymous-codon	KLHL28	GRCh38.p7	14:44945605	GTTTGCTGCTGGCAG[A/G]AGAGATTCAACTGTG	54813
rs756250167	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44943452	CACCTGAGGTCAGGA[A/G]TTTGAGATCGGCCTG	54813
rs756270301	snp	A/G/T	4.94444e-05	0.00497194	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963854	GTTTACTCCTGGAAC[A/G/T]TCTCAAACATAAGCA	54813
rs756297135	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44979007	CTAACCAATCCTACA[A/T]GTGGACAAAATAGAA	54813
rs756300811	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44965314	TATTTAAATTTCCCA[A/G]ATTGTCTCCAAAAGT	54813
rs756354317	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44977749	CTCCCAGGGTCAAGC[A/G]ATTCTCCTGCCTCAG	54813
rs756368978	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44931553	CACACTGCAAATATT[A/T]AAAAAAAATTTAATT	54813
rs756375076	in-del	-/A	1.64776e-05	0.00287028	intron-variant	KLHL28	GRCh38.p7	14:44944986	ACATTTAAAAAGCAT[-/A]AAAATCAATTAGCAT	54813
rs756410594	snp	C/T	1.64838e-05	0.00287083	missense	KLHL28	GRCh38.p7	14:44945810	TTAACATCACCTACT[C/T]GAAGAATGATGTCAC	54813
rs756440627	snp	C/T	1.65004e-05	0.00287227	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931433	TCCATTATGTCCACC[C/T]ACCACAAAAATAAAG	54813
rs756456671	in-del	-/TT			intron-variant	FAM179B	GRCh38.p7	14:44976647	TTTAAAAAAAAACTC[-/TT]TTAAAATAATACCTG	54813
rs756486383	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44934698	TCCAAAGTGGCAAAA[A/T]ATATAAAGTCAGATA	54813
rs756492113	snp	C/T	6.59402e-05	0.00574158	missense	KLHL28	GRCh38.p7	14:44934433	ACGCCAGGACGCACA[C/T]TAGTTGCAATACCAC	54813
rs756506804	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44970551	TTTCTTGTCTTATTG[C/T]ATTAGTTTGAACTTC	54813
rs756510795	snp	A/G	1.64876e-05	0.00287116	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963233	ATCAGGAGACAGAAG[A/G]AGAATCTGAGACAGC	54813
rs756562080	in-del	-/T			frameshift-variant	KLHL28	GRCh38.p7	14:44934267	AGATTGTAAATAAGA[-/T]TGTCCATCATAACCA	54813
rs756571450	in-del	-/A	1.65655e-05	0.00287793	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963546	GGCCGTCGAAGAACT[-/A]AAGCAGGTGCTGGGA	54813
rs756636213	snp	A/G	1.69318e-05	0.00290957	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964398	AGGAAAAAATAAATT[A/G]CCATGGGAAAATGAG	54813
rs756658203	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44971807	ACTTGTATGTAACTT[A/C]GAAGTGTATTTAGTC	54813
rs756704325	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44955259	TATATATAATACATA[A/G]AATACATGTGAGCTA	54813
rs756823215	snp	C/T			upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962050	GCGTTTACAACGTTC[C/T]GACTTCCTCTTCCAG	54813
rs756838580	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44939475	CCGCTTACCATTTAA[C/T]TATAAATTCCATTTT	54813
rs756930868	snp	C/T	2.18276e-05	0.00330353	intron-variant	KLHL28	GRCh38.p7	14:44934580	AATAAGCAGAAAAAA[C/T]ATAAAATTTAAAAAC	54813
rs756957290	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928726	CACGTTTTGTCTACA[C/T]GTACACTTATGAACA	54813
rs756990835	snp	C/G	1.64961e-05	0.00287189	missense	KLHL28	GRCh38.p7	14:44945465	ATGTATTTAGTGGCT[C/G]CCAAATAAAGGTCAC	54813
rs757020931	snp	A/T	1.66098e-05	0.00288177	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962574	AAACTACTACTTCCG[A/T]GGAGCTGCGGGGGAC	54813
rs757101350	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44938606	CAATCTCCTGACCTC[A/G]CGATCTGCCCGCCTT	54813
rs757139589	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44950496	TCAACATATGACACG[C/T]AAAAATGACACAACA	54813
rs757164099	snp	A/T	1.651e-05	0.0028731	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963713	GAGAGCAGGTACAGC[A/T]GTTCTTGGGACCAGT	54813
rs757174637	snp	A/G	1.6604e-05	0.00288127	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963630	GCTATATAATTTGTT[A/G]GACGATTCTAACTTC	54813
rs757226387	snp	A/G	1.68667e-05	0.00290397	intron-variant	KLHL28	GRCh38.p7	14:44929226	AGAAGATAGAAACAT[A/G]TTAACCATGAAGTAT	54813
rs757273110	snp	C/T	6.90679e-05	0.00587615	intron-variant	KLHL28	GRCh38.p7	14:44931571	AAAAAATTTAATTTA[C/T]AGATCTTTTGTGTCA	54813
rs757287462	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44972027	AGGAAGAGAGGGCAG[C/G]AGGAGATGCTACACA	54813
rs757347333	snp	A/G	0.000118814	0.00770669	missense, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44960900	ACCTGGTACAGAGCA[A/G]GGTAGGAATACTTGC	54813
rs757347482	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44969455	CCACGCCTGGCCTAT[C/G]AGATGTATCTTTTGA	54813
rs757357489	in-del	-/CAT	1.64751e-05	0.00287007	cds-indel, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964034	CTTTTGCCGTATTGG[-/CAT]CATCAATGGGCTCAG	54813
rs757365921	snp	A/G	1.64765e-05	0.00287019	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964132	ATGAATGCTGTGCAG[A/G]CCAGATTGGCTAGGA	54813
rs757458365	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942057	CTTCTTTGAGCTGTG[C/T]ACTCATATCCAGCTA	54813
rs757532479	snp	A/G	9.88435e-05	0.00702937	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44963979	CTTGCCCCAGCTCTT[A/G]TAGATAGCAAACGCA	54813
rs757560272	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44955941	TGCAATTGATTAAAC[A/G]ATATCAGATATTTTA	54813
rs757639925	in-del	-/TTA			intron-variant	KLHL28	GRCh38.p7	14:44934629	CAGATATGTTTAATC[-/TTA]TTAGTAATCAGGGAC	54813
rs757655366	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44953712	TCAGCCTCCATAACT[A/G]TAAGAAATAAATTCC	54813
rs757655865	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44946975	AGAAAGAAAAGAAAG[C/T]GGAGAGACAATAAAG	54813
rs757676346	snp	A/G	1.72279e-05	0.0029349	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964415	CATGGGAAAATGAGC[A/G]ACCTGGAATCATGGG	54813
rs757784356	snp	C/G	1.65146e-05	0.0028735	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963323	TTTCTCGTCTGCCCT[C/G]TGCCCTGAGGAGACA	54813
rs757832574	snp	A/C	6.69344e-05	0.0057847	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962727	TCGGCTCCTTCAACT[A/C]CTCCGCACTGCCCGG	54813
rs757912661	snp	A/G	1.68224e-05	0.00290016	intron-variant	KLHL28	GRCh38.p7	14:44934598	AAAATTTAAAAACCA[A/G]AGTGGCCCATAAAGA	54813
rs757932808	snp	A/G	1.65067e-05	0.00287282	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963350	GACACTACAATCGCC[A/G]CCTGGAGTCCCAGTT	54813
rs757933508	in-del	-/TGTGGA			intron-variant	KLHL28	GRCh38.p7	14:44933188	ACAGTTGGATGGATC[-/TGTGGA]TGTAGAACCCGTGGA	54813
rs757949997	in-del	-/AAG	6.68762e-05	0.00578218	intron-variant	KLHL28	GRCh38.p7	14:44929210	GGAAAGGTTGGCAAA[-/AAG]AAGATAGAAACATGT	54813
rs758003328	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958542	TAATTCAACTAATAA[C/T]GGTATATAATTCTAT	54813
rs758024775	snp	A/T	1.64827e-05	0.00287073	missense	KLHL28	GRCh38.p7	14:44945165	TACTTTAGGGCTTCA[A/T]TCAAAAGATGTTTAC	54813
rs758034347	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44936411	GTGAATGAAATCTAG[C/T]GAATAAGTAGAGAGG	54813
rs758112962	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44975574	CAGGTTCAAGCCATT[C/G]TCCCACCTCAGCCTC	54813
rs758139082	snp	A/G	3.30224e-05	0.00406326	missense, intron-variant	KLHL28	GRCh38.p7	14:44931416	CTGGACAAATGTGAG[A/G]CTCCATTATGTCCAC	54813
rs758160687	snp	A/C	1.65037e-05	0.00287256	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963746	TAGCAGCTTCTGTCA[A/C]AGTGCTGGCGGACAA	54813
rs758233052	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44950382	CAAGGTTATGAAGTA[C/T]TGACTAGATTCATTT	54813
rs758279706	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44946121	TCACATCATTCAACT[G/T]ATTTATTATAGATAT	54813
rs758286954	snp	C/G	1.65778e-05	0.002879	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962620	ACTACAACTTCGCCT[C/G]TGGCCTCGGCCCTCT	54813
rs758292354	snp	C/G	1.68363e-05	0.00290136	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962519	CTTCCGCCCCAGAGA[C/G]CGATGATAGTCGAGT	54813
rs758352445	snp	A/T	1.64901e-05	0.00287137	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963822	AATGAAGGAAGTAGG[A/T]CCTCAGCAGGTGCTT	54813
rs758464596	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44969005	TGTCACATACTTGGA[A/G]TTATACAGTAGCTTG	54813
rs758485147	snp	A/G	1.64735e-05	0.00286993	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963092	TACAACAAGGACTGG[A/G]AAGTACCGATGCCCG	54813
rs758492313	in-del	-/A			intron-variant	FAM179B	GRCh38.p7	14:44980283	ATACAAAATTTCCAG[-/A]AAAAAAATCATGAAT	54813
rs758579959	snp	A/T	1.64827e-05	0.00287073	missense	KLHL28	GRCh38.p7	14:44945330	CAAGACTCTAATGCA[A/T]AAAAAACAGTCTCTT	54813
rs758582924	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44939770	TTTCCCTATGGCCTC[G/T]TCTTCTGAGCCCTCA	54813
rs758672224	snp	C/T	1.64912e-05	0.00287147	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962965	AGCTTAGCACTTTTG[C/T]CTCAACTAGTTGTCT	54813
rs758720486	snp	A/G	1.6477e-05	0.00287024	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964221	TTCTGCCGGGGGTAG[A/G]TCAAACCATTTGGCA	54813
rs758780384	snp	A/C			missense	KLHL28	GRCh38.p7	14:44945395	TTCATCCAAGTCAGC[A/C]TGTGTAAGCTCAAAA	54813
rs758782619	snp	C/T	1.65089e-05	0.00287301	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963457	CTTTCCAACAGCAAT[C/T]TTAAATTTGGGATTA	54813
rs758807820	snp	A/C			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960494	AACTGTGAGAACCAG[A/C]CACTTTCTCATTGAC	54813
rs758862979	snp	G/T	3.29696e-05	0.00406001	synonymous-codon	KLHL28	GRCh38.p7	14:44934192	AGCAAAACAACTTCT[G/T]GTTGTCGTCATTGGT	54813
rs758876276	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44930997	AAACAGAACAATCCG[A/T]GGATTGTATGTATGT	54813
rs758951191	snp	C/G	1.89106e-05	0.00307489	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962371	GGGCTCCATCGAGCC[C/G]TTTGGAGACGGCAAT	54813
rs758993334	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44979253	TGTCTTAGACTGGGT[A/G]ATTTATAAACAATAG	54813
rs759013509	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44978675	TGGTGGCACATGTCT[A/G]TAGTCCCAGCTACTT	54813
rs759034945	snp	G/T	3.29489e-05	0.00405874	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963024	GAAAGATGCGCTGCA[G/T]ATCCTTCATATATGT	54813
rs759064308	snp	A/G			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960339	AGAAAGAGTGCACTG[A/G]ATTTTCAACTTGAAA	54813
rs759067400	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928217	ACACTGCTCAAATAT[C/T]TACATCAGCACTGGG	54813
rs759143404	snp	A/G	1.64898e-05	0.00287135	synonymous-codon	KLHL28	GRCh38.p7	14:44945533	ACAATTACCAGGATC[A/G]AGTTGGCTTTCAAGA	54813
rs759182642	snp	A/G	1.65154e-05	0.00287358	synonymous-codon, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929154	TGAGTGACCACCGAC[A/G]ACATAAAGGTAGTTA	54813
rs759229156	snp	C/G	1.6483e-05	0.00287076	missense	KLHL28	GRCh38.p7	14:44945422	AAAAAACTCTTCAGT[C/G]TGGCAAACAGCTTCA	54813
rs759326398	snp	G/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964199	AATATGCAGTACTGA[G/T]GCCATCTTCTGCCGG	54813
rs759393448	snp	A/T	1.8817e-05	0.00306727	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962410	CCAACCACCACCACC[A/T]GACAACCCTGCATGG	54813
rs759421503	snp	C/T	1.6531e-05	0.00287493	missense	KLHL28	GRCh38.p7	14:44934163	GCATATATCATTCCA[C/T]CCAATACCGCTGCAG	54813
rs759427266	snp	A/G	1.66849e-05	0.00288828	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962918	ACGTTCTCCGGGGTC[A/G]GGGGGAGGCAGGCCA	54813
rs759567109	snp	A/G	3.29522e-05	0.00405894	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964126	GGAGTGATGAATGCT[A/G]TGCAGGCCAGATTGG	54813
rs759615992	in-del	-/TTTCTTTCT			intron-variant	FAM179B	GRCh38.p7	14:44969151	TCCTTCCTTCCTTTC[-/TTTCTTTCT]TTTCTTTCTTTTCTT	54813
rs759616103	snp	C/T	1.6483e-05	0.00287076	synonymous-codon	KLHL28	GRCh38.p7	14:44934255	GTACTTCTCTACAGA[C/T]TGTAAATAAGATTGT	54813
rs759622975	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44947716	AATCCAACTCTTGAA[A/G]TTTTTATCTTTGTCA	54813
rs759629589	snp	A/G	1.73848e-05	0.00294824	synonymous-codon	KLHL28	GRCh38.p7	14:44934543	AGAGTCATTCTGAGG[A/G]AAGTACATCTCCACA	54813
rs759654991	snp	A/G	1.65086e-05	0.00287298	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964361	CAACTATCTGTACCC[A/G]AAGGGTATTAAGTGC	54813
rs759669154	in-del	-/ATGA			downstream-variant-500B	KLHL28	GRCh38.p7	14:44923816	ACTCCTGTTATACTT[-/ATGA]ATGTTTCTTTAGTAA	54813
rs759689847	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924855	ACATATGGATAACAA[C/T]TTTTCTCTCTGCAGA	54813
rs759698186	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961850	AAGGAAAATACCTGA[A/G]TCTCAGTAATCACAC	54813
rs759724527	snp	A/T	0.000189018	0.00971974	intron-variant	FAM179B	GRCh38.p7	14:44964503	TGAGTCGAAAGTGTG[A/T]AGAATTTAAATGAAA	54813
rs759747354	snp	A/G	1.64822e-05	0.00287068	stop-gained	KLHL28	GRCh38.p7	14:44945100	GAGCACAGCGAGGTC[A/G]TGTCATCAAGACTGT	54813
rs759759765	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44948557	AAAGTGATTCTCTAA[A/G]GTATAAAGTTCTACA	54813
rs759790788	snp	C/G	1.65086e-05	0.00287298	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963280	CAAATTGGGGAGCGA[C/G]TTGGCCAAGACAGGT	54813
rs759804447	snp	C/T	1.65293e-05	0.00287479	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963687	CCTGCATTTACTGGT[C/T]ATTCGCCTTGGAGAG	54813
rs759826905	snp	G/T	1.66158e-05	0.0028823	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931352	TCTAGGTTCTTTCAT[G/T]GGTCTACACACAGTC	54813
rs759910993	snp	A/G			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960227	TGCTTAAGTATCCAC[A/G]TCTCTCATTTAAGAC	54813
rs759917241	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44936447	GGGTTGGTCTTAGAA[A/G]TAACTTGGCAGATTT	54813
rs759983191	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44975395	CAGTGTGCATCTTGT[C/T]AAAGGACTTAGGTTC	54813
rs759998858	snp	A/G	1.74415e-05	0.00295304	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962490	TACCTATCGGCTCCA[A/G]AGCCGCAGTCGTCCT	54813
rs760040555	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44974400	TATTATCCTTTTGTT[C/T]TTACATGTTGTCTTT	54813
rs760042863	in-del	-/TC			intron-variant	FAM179B	GRCh38.p7	14:44971434	TATTAGTAATTTGTT[-/TC]TCTGTTTTTCTTAGC	54813
rs760051094	snp	C/T	1.66272e-05	0.00288328	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962562	GAGAGGAGAGAAAAA[C/T]TACTACTTCCGTGGA	54813
rs760076781	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926827	ATCATTTTCCACAGT[C/T]TTTCAAATTCCCTTA	54813
rs760128686	snp	C/T	4.94996e-05	0.00497467	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963795	AGAATACATGAAAAT[C/T]TTCCTCAAGCTAATG	54813
rs760150617	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942845	AAACTATCTTGATCG[C/T]TGCATAAACATTATG	54813
rs760299888	snp	A/C	1.6531e-05	0.00287493	missense, intron-variant	KLHL28	GRCh38.p7	14:44931501	CTGCCATGGATGCAA[A/C]CATCTCCCAGGAGTC	54813
rs760321592	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44976807	ATAGTAAATTTAAGA[A/T]TATGAAAGTGCTTCT	54813
rs760337851	snp	A/G	1.64963e-05	0.00287192	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963804	GAAAATCTTCCTCAA[A/G]CTAATGAAGGAAGTA	54813
rs760354277	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44964799	GATAAAGAGCTAAAT[A/T]CTGGGAATGAAGATG	54813
rs760387993	snp	A/G	1.65359e-05	0.00287536	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931382	CCACTGATTTTGATG[A/G]GGATCGTATCTTTCA	54813
rs760409910	in-del	-/GTAATTTA			intron-variant	FAM179B	GRCh38.p7	14:44971888	AAGAACTGAGACAAG[-/GTAATTTA]TAAAGAAAAGAGACT	54813
rs760426944	in-del	-/AAAT			intron-variant	KLHL28	GRCh38.p7	14:44956627	ACTAAATTCTTCAAC[-/AAAT]AAACTGCAAGAAATA	54813
rs760436407	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44969946	GATTACTGTAGCTTT[A/G]TAGTAAATCTTGAAG	54813
rs760437512	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927957	TTTTGGATGTTAACA[C/T]TGGCGTAATCACTAA	54813
rs760515287	snp	A/C	1.64751e-05	0.00287007	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964208	TACTGATGCCATCTT[A/C]TGCCGGGGGTAGGTC	54813
rs760566038	snp	A/G	1.64836e-05	0.0028708	missense	KLHL28	GRCh38.p7	14:44945450	TCAAAATTCTGGCAT[A/G]TGTATTTAGTGGCTG	54813
rs760581540	snp	A/G	1.64833e-05	0.00287078	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964334	GCATGCACATTTATG[A/G]ATCTTACAGCCCAAC	54813
rs760719137	snp	A/G	1.64735e-05	0.00286993	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963068	CTGGAGAGGTGCTGA[A/G]AACGCTTATACAACA	54813
rs760724597	in-del	-/A			intron-variant	KLHL28	GRCh38.p7	14:44942128	AAACTCAATGTGTCC[-/A]AAACTCTTCCCCTGA	54813
rs760772713	snp	C/T	1.73898e-05	0.00294866	intron-variant	KLHL28	GRCh38.p7	14:44945950	AAAAATAAAAAAGCA[C/T]AGACAGTTATTTCAA	54813
rs760806466	snp	C/G	1.65119e-05	0.00287327	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963314	AATCTTACATTTCTC[C/G]TCTGCCCTCTGCCCT	54813
rs760856459	snp	A/C/T	3.29789e-05	0.00406061	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963423	ATTTCCTGAAGATCC[A/C/T]CTTCCCTGTGCAGTG	54813
rs760912655	snp	C/G/T	3.30837e-05	0.00406706	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963522	GGAAGACTATAAGAA[C/G/T]CGGACCCAGGCCGTC	54813
rs760914139	snp	C/T			missense	KLHL28	GRCh38.p7	14:44945081	ACTGCACAAAGTACT[C/T]TGGGAGCACAGCGAG	54813
rs761024442	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44975776	CCGGCTTCCCCTGCC[-/T]TTTTTTTTTTTTTTA	54813
rs761030710	snp	C/T			intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937357	TTTCACTATATTGGC[C/T]AGGCTGGTCTCGAAC	54813
rs761049120	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44973281	AGTAGTTTCCCTAGA[A/G]TGTGTAATACACATT	54813
rs761111144	snp	A/G	1.64846e-05	0.0028709	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963908	TGAACATTTGCATCT[A/G]CTCCCTGCTGACCTA	54813
rs761111215	snp	G/T	3.3232e-05	0.00407614	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962570	AGAAAAACTACTACT[G/T]CCGTGGAGCTGCGGG	54813
rs761129045	snp	A/T	1.6557e-05	0.00287719	intron-variant	KLHL28	GRCh38.p7	14:44934569	CCACACTAAAGAATA[A/T]GCAGAAAAAATATAA	54813
rs761150958	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44949525	ATACCCCCCAGAGTA[C/T]ACCACTTAATGGAAT	54813
rs761160067	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44965693	TTGGATAAGGTGGTA[A/G]TAGCCAGATCTCTCC	54813
rs761197684	snp	C/G	1.64803e-05	0.00287052	synonymous-codon	KLHL28	GRCh38.p7	14:44945125	GACTGTCTGATGAGA[C/G]AGTCTATGTTCAGGC	54813
rs761223153	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940625	ACTAAAGCCATTGGA[C/T]AAGTGCTGTTTTAAA	54813
rs761227117	snp	A/G	4.948e-05	0.00497369	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963810	CTTCCTCAAGCTAAT[A/G]AAGGAAGTAGGACCT	54813
rs761233044	snp	A/G	3.37348e-05	0.00410685	missense, intron-variant	KLHL28	GRCh38.p7	14:44931534	TACTTGGATCATAAC[A/G]CTCCACACTGCAAAT	54813
rs761270049	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44954394	TGTTTCTTATTCCTC[A/G]TATTTGAGAGACCAA	54813
rs761305111	snp	C/T	1.65919e-05	0.00288022	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962700	TTTGTCAGGGGGAGA[C/T]GAAGAGGACACTCGG	54813
rs761486247	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44976727	TGTATAGTCAATAAG[A/G]CCAGCACATGATACT	54813
rs761497297	snp	A/C			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925639	TCCCACAGCATCTAA[A/C]AGAATATCTCATACA	54813
rs761503450	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44938411	GAGTCTCGCTCTATC[C/G]CCCAGGCTGGAGTGC	54813
rs761535505	in-del	-/G			intron-variant	KLHL28	GRCh38.p7	14:44942320	AACATTTTTTAAAAT[-/G]AATGCCCCATTCTCT	54813
rs761582121	snp	C/T	1.71537e-05	0.00292857	missense	KLHL28	GRCh38.p7	14:44934122	TTAAATACCTGTTCA[C/T]GTGGGCAGGACCATA	54813
rs761606982	snp	C/T	1.64811e-05	0.00287059	missense	KLHL28	GRCh38.p7	14:44945711	AACTCAACCTCACTG[C/T]TCTCTTTTTCAGAAA	54813
rs761645890	in-del	-/AAAT			intron-variant	KLHL28	GRCh38.p7	14:44955786	TGAGGCCCTGCCTCA[-/AAAT]AAATAAATAAATAAA	54813
rs761670849	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44932055	TTGAGGCAGGTCTCG[C/T]TCTGTCACCTAGGCT	54813
rs761680880	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924351	TTTTATTTTAAACAT[C/T]TTACATTAAATGAAA	54813
rs761691848	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44969657	TTTCTCCTATGTTAT[C/G]TTCTAGGCATTTTAT	54813
rs761704972	in-del	-/AGGC	1.6612e-05	0.00288196	upstream-variant-2KB, frameshift-variant, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962924	TCCGGGGTCAGGGGG[-/AGGC]AGGCCAGCTTGAAGA	54813
rs761724287	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44946133	ACTTATTTATTATAG[A/T]TATTAGGAAATGGAA	54813
rs761724399	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44930400	CTCCCGAGTAGCTGA[C/T]ACTACAGGCATGTGC	54813
rs761762101	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44952868	GTTTCATTTACCTCA[A/G]TAACCACTTTGCGTA	54813
rs761849715	snp	C/G	1.64904e-05	0.00287139	missense	KLHL28	GRCh38.p7	14:44945571	AACATTCTTTCAGGA[C/G]AAGTTTTATCTGGAG	54813
rs761877774	snp	A/G	1.65094e-05	0.00287305	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963274	CTTCAACAAATTGGG[A/G]AGCGACTTGGCCAAG	54813
rs761893347	snp	A/C	1.64836e-05	0.0028708	missense	KLHL28	GRCh38.p7	14:44934260	TCTCTACAGATTGTA[A/C]ATAAGATTGTCCATC	54813
rs761902461	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44935411	TACATTTGGGATTTG[C/T]ACATTTTTCTGCATG	54813
rs761961954	in-del	-/TAA			intron-variant	FAM179B	GRCh38.p7	14:44979175	ATAAGTCACCATTAA[-/TAA]TAATAATAATAATAA	54813
rs761983173	snp	A/C	1.87929e-05	0.00306531	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962426	GACAACCCTGCATGG[A/C]GGCTGCCCCCTCCGC	54813
rs762044241	snp	G/T	1.81714e-05	0.0030142	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962463	TCTGCTGCCGCCCTT[G/T]CCAGTCCTCTCTACC	54813
rs762080143	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44957844	CAGAATTTCTTAATC[G/T]TATTAAAATCTTAAC	54813
rs762147812	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44977232	GAAAATTAGACAGAC[-/T]TTTTTTTTTTTTTTT	54813
rs762150341	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44948133	GGAAAGGCAAGTAGA[C/T]AGAAAAAATAGGTAA	54813
rs762240247	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44949275	ATACCGATAAGAAGA[C/T]GTAGAGATCTTTAGG	54813
rs762244443	snp	A/G	1.64933e-05	0.00287165	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963431	AAGATCCCCTTCCCT[A/G]TGCAGTGACTCTTTC	54813
rs762282458	snp	A/C	3.29614e-05	0.00405951	missense	KLHL28	GRCh38.p7	14:44945144	CTATGTTCAGGCATA[A/C]AGTGGTACTTTAGGG	54813
rs762367793	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44952674	CAGTAGCTGGGACTA[C/T]AGGTGTCCACCACTG	54813
rs762380216	snp	C/T	1.66106e-05	0.00288184	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928981	CCATCCGGATGTTCA[C/T]GCAGTACAAGTTTCA	54813
rs762405947	in-del	-/AGA	1.64844e-05	0.00287087	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963228	TGGTGATCAGGAGAC[-/AGA]AGAAGAATCTGAGAC	54813
rs762422932	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44968597	AGCAACTTTCAACAG[A/C]GAGTACAGATAGTTC	54813
rs762453513	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44931209	TACCACATACAAGTC[-/T]TTTTTTTTTTTTTTT	54813
rs762463533	snp	G/T	1.64762e-05	0.00287016	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963005	AAGAGAATCCAGCCC[G/T]GCGGAAAGATGCGCT	54813
rs762476519	snp	A/G	1.64863e-05	0.00287104	synonymous-codon	KLHL28	GRCh38.p7	14:44945227	TTCATATAGTCTAGT[A/G]AGAAACTTAACACTC	54813
rs762532561	in-del	-/TTTTATAGAAAAAGTCT			intron-variant	KLHL28	GRCh38.p7	14:44944432	ATTTACTGTTTGGTC[-/TTTTATAGAAAAAGTCT]GACAATTCCTAATCT	54813
rs762610031	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44953863	GAAAAAATAGGTAAA[A/C]CTGATTACATTTTAA	54813
rs762614054	snp	A/T	1.64849e-05	0.00287092	synonymous-codon	KLHL28	GRCh38.p7	14:44945266	TAATCGTACACTGTT[A/T]AGTAACTGTGCTAAG	54813
rs762618919	snp	A/C			synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964008	CAGGGTACGCCAAGC[A/C]GCTTTAGAAGCTTTT	54813
rs762625126	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44939311	GATCTTAAAATGCCT[C/T]CAGGGCCTTTCTCCC	54813
rs762651162	snp	A/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928755	CATAAAACTAGTACA[A/T]CTCAGTCTTGGGGGA	54813
rs762706089	snp	A/T	1.70336e-05	0.00291831	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962862	AGTGCTTGTGGAAGG[A/T]GGTAGTGATGAGAAG	54813
rs762773740	snp	A/C	1.67654e-05	0.00289524	missense	KLHL28	GRCh38.p7	14:44934137	TGTGGGCAGGACCAT[A/C]CCCACCAATGGCATA	54813
rs762806205	snp	A/G	1.64833e-05	0.00287078	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963928	CTGCTGACCTATCCT[A/G]GTGAGGATTTTGACT	54813
rs762838233	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44979994	GCAAAGTATATTAGT[A/G]TTATAATATTGAAAA	54813
rs762853210	snp	A/G	1.64882e-05	0.00287121	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963390	GGTTCCTTATTATTT[A/G]GAACTTGAAGCCTCT	54813
rs762883264	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44959605	GAAATAAAGTAAGTT[C/T]TTAGGGCAATTGTGT	54813
rs762893744	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44978941	GAGTTCAAGGCCAGA[C/T]TAGTCAACATTGCAA	54813
rs762911017	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44966534	TTTAAAAAATTGTGA[C/T]ATTTCTTCTCTGTTT	54813
rs762936212	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44948929	CTCTGTAAAACATAC[A/C]CCTTTCAACTCTCAT	54813
rs763014287	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44949149	TCATTACCAGTGCCA[C/T]AGGACTGAAGACTAT	54813
rs763034727	snp	C/T	1.78039e-05	0.00298356	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962478	TCCAGTCCTCTCTAC[C/T]TATCGGCTCCAGAGC	54813
rs763048159	snp	A/G	1.66665e-05	0.00288669	missense	KLHL28	GRCh38.p7	14:44945912	GCAAGCATGTAGGTC[A/G]GGGATGTGTGGTCCA	54813
rs763065681	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44947831	AACAGCCTCCACTGC[C/T]GATCTCTGCAAATAA	54813
rs763226531	snp	A/C	1.6483e-05	0.00287076	synonymous-codon	KLHL28	GRCh38.p7	14:44934414	TTCATGTTTTCTGAT[A/C]GTGACGCCAGGACGC	54813
rs763283424	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44939101	AAGCTTACTACTTGT[A/G]CCTTCTAGAGTAGCA	54813
rs763375423	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44973877	AAGTTAGATGTAATT[A/C]TTATCTTTGCTCCCC	54813
rs763376542	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44976587	TGTTTGTTCAGTGAA[C/T]TAAAGTTATCTCAAG	54813
rs763378716	snp	A/C			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925194	AGTTTACTGAACTTT[A/C]AGCAGTAAGTGTTTA	54813
rs763405402	snp	C/G/T	3.2948e-05	0.00405871	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963116	ATGCCCGACTTAGAG[C/G/T]TTCCACAGCACTACT	54813
rs763422551	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44975466	ACCGTTCCCCTTTTT[C/T]TGTTTGTTTGTTTTG	54813
rs763432407	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44940377	GAGTTTCATTCTTGA[A/T]TTAGACCTGTGGTTT	54813
rs763449585	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44941615	CCTGGGCAACAACAG[C/T]GAAACTCTGTCTCAA	54813
rs763456062	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927862	TATCTAGCACAAGAA[A/G]AAAGAAGATCAAAAG	54813
rs763473895	snp	A/G	1.65378e-05	0.00287552	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963681	TGAAGTCCTGCATTT[A/G]CTGGTTATTCGCCTT	54813
rs763564692	snp	A/G	3.30622e-05	0.00406571	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931388	ATTTTGATGAGGATC[A/G]TATCTTTCAATGCTG	54813
rs763594732	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44952691	GGTGTCCACCACTGC[A/G]TTTGGCTCAAAAACT	54813
rs763609706	snp	C/T	1.65127e-05	0.00287334	missense, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929150	ACCCTGAGTGACCAC[C/T]GACGACATAAAGGTA	54813
rs763652449	snp	A/G	1.67514e-05	0.00289403	intron-variant	KLHL28	GRCh38.p7	14:44929212	AAAGGTTGGCAAAAA[A/G]AAGATAGAAACATGT	54813
rs763694980	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44946672	AATGATTCTCCTGCT[G/T]AGCCTCCCAAGTAGC	54813
rs763719388	snp	A/G	3.2981e-05	0.00406071	synonymous-codon	KLHL28	GRCh38.p7	14:44945554	GCTTTCAAGAAATGC[A/G]CAACATTCTTTCAGG	54813
rs763816609	snp	C/T			downstream-variant-500B	KLHL28	GRCh38.p7	14:44923922	TTGTCCAGGCTGGAA[C/T]GCAATGGCGCCATCT	54813
rs763855732	snp	C/G/T	3.29904e-05	0.00406132	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963806	AAATCTTCCTCAAGC[C/G/T]AATGAAGGAAGTAGG	54813
rs763867713	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44939425	CTTTTCACTTTTTAC[A/G]TGGTCAAGCTGCTAA	54813
rs763931517	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44951620	AAAGAAAAGGCACTG[A/G]TAAAAGTAACTTCAT	54813
rs763941888	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44930114	AAGTTCTCATTGTTT[A/C]TGTGGCTTTCCCTCT	54813
rs764023388	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964212	GATGCCATCTTCTGC[C/T]GGGGGTAGGTCAAAC	54813
rs764024103	snp	A/G	1.64855e-05	0.00287097	synonymous-codon	KLHL28	GRCh38.p7	14:44945458	CTGGCATATGTATTT[A/G]GTGGCTGCCAAATAA	54813
rs764037716	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44944864	GAATGAATGACAATA[C/T]AATAAAAACAATCAC	54813
rs764059034	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44980043	TAACCTTATTTAGTA[G/T]CTGAAGCTGGCCTCC	54813
rs764077021	snp	C/T	0.000115328	0.0075928	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964122	AGATGGAGTGATGAA[C/T]GCTGTGCAGGCCAGA	54813
rs764100355	snp	G/T	1.64746e-05	0.00287002	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963143	TACTGCTTCCCATCT[G/T]GCTTACTACTGAGGA	54813
rs764122155	snp	G/T	1.65138e-05	0.00287343	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963315	ATCTTACATTTCTCG[G/T]CTGCCCTCTGCCCTG	54813
rs764209357	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44970271	ATTTTGCTAAATTTA[C/G]ATTGAAATATCCTAC	54813
rs764219045	in-del	-/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961012	TTCAAAAAAAAAAAA[-/T]ATCTCTTCCACACTC	54813
rs764272064	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44969432	GCTGGGATTACAGGT[A/G]CAAGCTACCACGCCT	54813
rs764498098	snp	A/G	2.03411e-05	0.00318907	intron-variant	KLHL28	GRCh38.p7	14:44934572	CACTAAAGAATAAGC[A/G]GAAAAAATATAAAAT	54813
rs764532191	snp	A/G	1.66114e-05	0.00288192	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962705	CAGGGGGAGATGAAG[A/G]GGACACTCGGCTCCT	54813
rs764541583	snp	C/T	1.64806e-05	0.00287054	missense	KLHL28	GRCh38.p7	14:44945132	TGATGAGAGAGTCTA[C/T]GTTCAGGCATAAAGT	54813
rs764596439	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44957679	CCTCAGAGCAACAAT[A/G]TAATAGGCACTGTTA	54813
rs764618267	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925363	ATATTTAAAATTTCT[A/G]TAGTTTTCTTACTAG	54813
rs764619463	snp	C/T	3.29522e-05	0.00405894	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963196	ACCGAGGTGATAATA[C/T]CCCTAGCCCGAAAGC	54813
rs764620129	snp	C/T	9.96893e-05	0.00705937	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962572	AAAAACTACTACTTC[C/T]GTGGAGCTGCGGGGG	54813
rs764773951	in-del	-/ATA			intron-variant	KLHL28	GRCh38.p7	14:44933095	ATCTCTAGATTACTT[-/ATA]ATACTATGCAAATAG	54813
rs764785667	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44949871	TGCATTAACAGAACT[A/G]TAATATACAGAACTA	54813
rs764835752	snp	C/T			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960663	ATTTAAACCAAAACA[C/T]AGGATGTATATTTAC	54813
rs764844631	in-del	-/TTTCT	3.30235e-05	0.00406333	upstream-variant-2KB, frameshift-variant, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962946	CAGCTTGAAGAGGCC[-/TTTCT]TTTAGCTTAGCACTT	54813
rs764845901	snp	A/C	1.64923e-05	0.00287156	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963815	TCAAGCTAATGAAGG[A/C]AGTAGGACCTCAGCA	54813
rs764878062	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44957348	AAATATAAGGCACAA[A/C]ATTTTGAATAAGACA	54813
rs764927134	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44931696	AGGTTTTGCTGATAA[A/G]ATTGCAAAGATAAAA	54813
rs764963662	snp	A/C			intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937593	GAGATGATTTAGCTA[A/C]ATACATACAACATAC	54813
rs765020386	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44941911	AATCCTTTTTCCTCT[C/T]TATATTTTCTCACCA	54813
rs765117624	snp	C/T	1.65146e-05	0.0028735	missense, intron-variant	KLHL28	GRCh38.p7	14:44931410	TCAATGCTGGACAAA[C/T]GTGAGACTCCATTAT	54813
rs765163069	snp	A/G	3.46272e-05	0.00416082	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931541	ATCATAACGCTCCAC[A/G]CTGCAAATATTTAAA	54813
rs765186981	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926972	TTTAAACTGCTTTTC[C/T]TTAAATAAAGTCTGG	54813
rs765204303	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44978730	TGAGCCTGGGAGGTC[A/G]AGGCTGTAATAAGCT	54813
rs765237561	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44977379	ACCTGGGACTACAGG[C/T]ACCCGCCACCATGCC	54813
rs765318218	snp	A/T	1.64819e-05	0.00287066	missense	KLHL28	GRCh38.p7	14:44934398	AGCATTCCACTGAAT[A/T]TTCATGTTTTCTGAT	54813
rs765325019	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44978803	AGACCTTGTCTCAAA[A/G]ATTAAAAAAAAGAGA	54813
rs765343578	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44948806	GATCTTCCTTTCCTC[A/C]AATTCAAATTCTCAA	54813
rs765370490	snp	A/G	9.87118e-05	0.00702468	utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44960936	AAGTGCATAAATTTG[A/G]GTCTTCAAATGATAA	54813
rs765370787	snp	A/C	1.65614e-05	0.00287757	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963542	CCCAGGCCGTCGAAG[A/C]ACTAAAGCAGGTGCT	54813
rs765415315	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44968844	TATCCATGTCTTGTA[C/T]CCACCATTATAGTAT	54813
rs765484007	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44969974	AAGTTCCGTAGTGTC[A/G]GTCTTCTGACTTTGT	54813
rs765486027	snp	A/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964141	GTGCAGGCCAGATTG[A/G]CTAGGAAAACCTTAC	54813
rs765524437	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44974433	TCATTATAGCCCTTA[A/G]TATATTAATTATAGT	54813
rs765527097	snp	A/C	3.29658e-05	0.00405978	synonymous-codon	KLHL28	GRCh38.p7	14:44934264	TACAGATTGTAAATA[A/C]GATTGTCCATCATAA	54813
rs765554308	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44971436	TTAGTAATTTGTTTC[C/T]CTGTTTTTCTTAGCC	54813
rs765584166	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44968698	AATCAGTGAACCCAT[A/T]TTAACATATAATTAT	54813
rs765654123	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44936473	GATTTGGTGTTGGGA[A/C]GATGAGGTAGTTCTC	54813
rs765664066	snp	A/G	1.64852e-05	0.00287094	synonymous-codon	KLHL28	GRCh38.p7	14:44945244	GAAACTTAACACTCA[A/G]CAATGGTAATCGTAC	54813
rs765708494	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961887	CGACAGGAGGAGGAA[C/T]CGCGGACAACTGGAG	54813
rs765749477	snp	C/G	3.30044e-05	0.00406216	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963446	GTGCAGTGACTCTTT[C/G]CAACAGCAATCTTAA	54813
rs765761460	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44975404	TCTTGTTAAAGGACT[C/T]AGGTTCCATATTTTC	54813
rs765851774	snp	C/T	1.67525e-05	0.00289413	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962911	CTCTCGGACGTTCTC[C/T]GGGGTCAGGGGGAGG	54813
rs765876852	in-del	-/G	3.29935e-05	0.00406149	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963247	GAAGAATCTGAGACA[-/G]CTTTCTCCGCACTTC	54813
rs765878115	snp	A/C	3.32347e-05	0.00407631	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928988	GATGTTCATGCAGTA[A/C]AAGTTTCACCACCAT	54813
rs765887376	snp	A/G	1.64833e-05	0.00287078	synonymous-codon	KLHL28	GRCh38.p7	14:44945169	TTAGGGCTTCATTCA[A/G]AAGATGTTTACAAGT	54813
rs765929132	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44977515	TGCTGGGATTACAGG[C/T]GTGAGCCACAGCACC	54813
rs765929204	snp	A/G	4.95381e-05	0.0049766	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963706	CGCCTTGGAGAGCAG[A/G]TACAGCAGTTCTTGG	54813
rs765938119	snp	A/T	3.29538e-05	0.00405904	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964113	AGATAATGGAGATGG[A/T]GTGATGAATGCTGTG	54813
rs765977060	snp	C/G	1.64852e-05	0.00287094	missense	KLHL28	GRCh38.p7	14:44945272	TACACTGTTTAGTAA[C/G]TGTGCTAAGTATTTC	54813
rs765980071	snp	C/T	1.67801e-05	0.00289651	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962731	CTCCTTCAACTCCTC[C/T]GCACTGCCCGGGATC	54813
rs765984051	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926868	ATAGGGGATTAAAAA[C/T]AGTATAATAGGATAT	54813
rs765996151	snp	G/T	3.2962e-05	0.00405954	missense	KLHL28	GRCh38.p7	14:44945396	TCATCCAAGTCAGCA[G/T]GTGTAAGCTCAAAAA	54813
rs766065391	snp	C/T	6.63823e-05	0.00576079	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928995	ATGCAGTACAAGTTT[C/T]ACCACCATACTATTT	54813
rs766081210	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44956654	AGAAATAAAGAGAAT[G/T]AATCTATAAATTTAA	54813
rs766093538	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44954494	AGAGCATCCACACAA[C/T]GCAGTACTATACAGC	54813
rs766190011	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927266	TCAAATCTACAACTG[A/G]CAGTTTATGGAAGAA	54813
rs766204763	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925846	CTATTACAACATCCA[A/G]TGATTATTGAATAGC	54813
rs766242008	snp	A/G	9.2681e-05	0.00680675	intron-variant	KLHL28	GRCh38.p7	14:44931548	CGCTCCACACTGCAA[A/G]TATTTAAAAAAAATT	54813
rs766258131	snp	C/T	0.00046761	0.0152835	missense	KLHL28	GRCh38.p7	14:44945919	TGTAGGTCGGGGATG[C/T]GTGGTCCATCTACAG	54813
rs766302805	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44959765	TATCCTTAACCACTT[C/T]CTTTTAACTTTCTGA	54813
rs766322980	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44955660	ATGTGGTGGCACATG[C/T]CTGTAGTCTCAGCTA	54813
rs766332119	snp	C/T	1.64803e-05	0.00287052	missense	KLHL28	GRCh38.p7	14:44945766	AATACGGGCTGACGC[C/T]GGCAAGTACCACTTT	54813
rs766336826	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940917	CCAGCCTGACCAACA[C/T]GGTGAAACCCTGTTT	54813
rs766397772	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44951179	ATGGGGTCAAAAGTC[-/T]TAACACCTAATCACA	54813
rs766454621	snp	A/G	3.32651e-05	0.00407817	synonymous-codon	KLHL28	GRCh38.p7	14:44934147	ACCATACCCACCAAT[A/G]GCATATATCATTCCA	54813
rs766478086	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44974735	ATTTTAAAAAAGAGA[A/G]TTCTTGATGCCTTTA	54813
rs766496503	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44977280	TGCTCTGTTGCCCAG[C/G]CTGGAGTGTAGTAGT	54813
rs766523116	snp	C/T	4.94442e-05	0.00497188	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964250	CACATGGAGCAGATA[C/T]GGACTGGCTTTTGGC	54813
rs766688523	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44930534	CTCCCAAAGTGCTAG[A/G]ATTACAGGTGTGAGC	54813
rs766712676	snp	A/G	1.65855e-05	0.00287967	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963568	GTGCTGGGAAAATTT[A/G]ACCCTAGTTCTACTC	54813
rs766717399	snp	C/G			missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964353	TTACAGCCCAACTAT[C/G]TGTACCCGAAGGGTA	54813
rs766719339	snp	C/T	1.64735e-05	0.00286993	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963099	AGGACTGGAAAGTAC[C/T]GATGCCCGACTTAGA	54813
rs766739761	snp	A/G			synonymous-codon	KLHL28	GRCh38.p7	14:44945092	TACTTTGGGAGCACA[A/G]CGAGGTCGTGTCATC	54813
rs766757580	snp	A/G	3.30273e-05	0.00406356	synonymous-codon, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929151	CCCTGAGTGACCACC[A/G]ACGACATAAAGGTAG	54813
rs766800061	snp	A/G	1.65329e-05	0.0028751	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963684	AGTCCTGCATTTACT[A/G]GTTATTCGCCTTGGA	54813
rs766818040	in-del	-/CAT	2.22839e-05	0.00333788	intron-variant	KLHL28	GRCh38.p7	14:44931293	CATCATTATAGAAAA[-/CAT]TGCCTTACATGTTTA	54813
rs766827141	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44951161	TCTATTCTAAGGGTG[C/T]GGGATGGGGTCAAAA	54813
rs766839891	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44968364	TCCCGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC	54813
rs766951662	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44973341	GTAACAATATACTGC[A/T]TCACAGGTAACCCAA	54813
rs767029840	snp	A/C			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926791	GGGATTACAGGCGTG[A/C]GCCACTGCGCCCGTC	54813
rs767066536	snp	A/G			synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963495	GGAGCTGCATTCACG[A/G]TTATTGGATCAGGAA	54813
rs767081724	snp	A/G	4.94222e-05	0.00497078	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963032	CGCTGCAGATCCTTC[A/G]TATATGTCTGAAACG	54813
rs767083749	snp	C/G	1.64827e-05	0.00287073	missense	KLHL28	GRCh38.p7	14:44945298	ATTTCTGGCGTTCTT[C/G]TACATCATACTTGAT	54813
rs767142056	snp	C/T	1.65581e-05	0.00287728	missense, intron-variant	KLHL28	GRCh38.p7	14:44931366	TTGGTCTACACACAG[C/T]CCACTGATTTTGATG	54813
rs767177292	snp	A/C	1.64765e-05	0.00287019	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964130	TGATGAATGCTGTGC[A/C]GGCCAGATTGGCTAG	54813
rs767205283	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925700	TCAAAATAAAATTTC[A/G]AAACCTAATGCCATT	54813
rs767240208	snp	C/T			upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962058	AACGTTCTGACTTCC[C/T]CTTCCAGGAGACTTT	54813
rs767244879	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44968697	TAATCAGTGAACCCA[C/T]ATTAACATATAATTA	54813
rs767290666	snp	G/T	1.66048e-05	0.00288134	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963599	CTCATTCTAGTCTTG[G/T]TGGCTTCATTAGTTT	54813
rs767318851	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44956018	CACCGGACGATGCTA[A/G]TGTAGCAACTCATTT	54813
rs767319210	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44976735	CAATAAGACCAGCAC[A/G]TGATACTGGGGTTCT	54813
rs767420711	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44954406	CTCATATTTGAGAGA[C/T]CAAAAGGCAACTGAC	54813
rs767457739	snp	C/G	9.90638e-05	0.00703719	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962946	CCAGCTTGAAGAGGC[C/G]TTTAGCTTAGCACTT	54813
rs767472151	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44969722	TTGGAGTTAATTTTT[A/G]TGAAGGGTGTCAGGT	54813
rs767474128	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44952880	TCAGTAACCACTTTG[C/T]GTAAAAGGAAGGGTA	54813
rs767480597	snp	A/G	1.65151e-05	0.00287355	synonymous-codon	KLHL28	GRCh38.p7	14:44934167	ATATCATTCCATCCA[A/G]TACCGCTGCAGCAAA	54813
rs767488600	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44932114	TGCAGCCTCAAATTC[C/T]GGGGCTAAAGTGATC	54813
rs767503711	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964200	ATATGCAGTACTGAT[A/G]CCATCTTCTGCCGGG	54813
rs767532812	snp	A/G	1.65641e-05	0.00287781	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964373	CCCGAAGGGTATTAA[A/G]TGCAGGAAAAGGAAA	54813
rs767555273	snp	C/G	1.82237e-05	0.00301853	splice-acceptor-variant	KLHL28	GRCh38.p7	14:44934559	AAGTACATCTCCACA[C/G]TAAAGAATAAGCAGA	54813
rs767585260	snp	A/G	3.79485e-05	0.00435578	intron-variant	FAM179B	GRCh38.p7	14:44964513	GTGTGAAGAATTTAA[A/G]TGAAAATATGCCCGT	54813
rs767650214	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44955970	TAAATGCATGAGTTA[A/G]TAATGATACTTAAAA	54813
rs767714808	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44948220	TTTGCAGAATGAGAT[A/C]ATAATAATACCTGTA	54813
rs767737154	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44959767	TCCTTAACCACTTCC[-/T]TTTAACTTTCTGAGG	54813
rs767783497	snp	A/G	1.65108e-05	0.00287317	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963307	AGGTTTCAATCTTAC[A/G]TTTCTCGTCTGCCCT	54813
rs767885713	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958016	ATTGCCTTCCAGTAT[C/T]TGCCTAAAAGCAGAT	54813
rs768087931	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44969581	TCAGTTTTTTCTTGC[A/G]TGGATCATGCCTTTG	54813
rs768096920	snp	C/T	1.64841e-05	0.00287085	missense	KLHL28	GRCh38.p7	14:44934422	TTCTGATAGTGACGC[C/T]AGGACGCACATTAGT	54813
rs768100798	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44949296	GATCTTTAGGATTAG[A/G]ATATATGAGCTAAAA	54813
rs768105823	snp	A/G	1.65072e-05	0.00287286	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963268	TCCGCACTTCAACAA[A/G]TTGGGGAGCGACTTG	54813
rs768135712	in-del	-/TCTT	1.64988e-05	0.00287213	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963441	TCCCTGTGCAGTGAC[-/TCTT]TCCAACAGCAATCTT	54813
rs768178626	snp	A/G	6.59859e-05	0.00574357	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963370	GAGTCCCAGTTTGGA[A/G]GTCAGGTTCCTTATT	54813
rs768217846	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44954169	AAACAGGAAATCTCA[C/T]TCATTGCTGTGGGAA	54813
rs768228930	snp	G/T	1.94956e-05	0.00312209	intron-variant	KLHL28	GRCh38.p7	14:44934089	AAATCCATAAACATA[G/T]GCAATTTAATTATTA	54813
rs768324011	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44955454	AACTCCTTGGGCAGA[C/T]AGCTGATACCATGTC	54813
rs768375079	snp	C/T	1.65553e-05	0.00287705	missense	KLHL28	GRCh38.p7	14:44945889	CAGAATGCAAGTGGG[C/T]TAAGTTAGCAAGCAT	54813
rs768450823	in-del	-/GTAT	1.65231e-05	0.00287424	frameshift-variant, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964366	ATCTGTACCCGAAGG[-/GTAT]TAAGTGCAGGAAAAG	54813
rs768492562	snp	A/C			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924559	TTAAACTAACATAAT[A/C]CACAACTAGATCACA	54813
rs768522453	snp	C/T	1.76452e-05	0.00297024	intron-variant	KLHL28	GRCh38.p7	14:44944991	TTAAAAAGCATAAAA[C/T]CAATTAGCATCATTC	54813
rs768591449	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44931862	CGAACCTTAACCCTA[C/T]TGCTGTGGATTTGTG	54813
rs768687047	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44979031	ATAGAAATAACAGAT[-/T]AAAAAAAAAAGGTTA	54813
rs768699804	in-del	-/A	1.66757e-05	0.00288749	upstream-variant-2KB, frameshift-variant, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962544	CGAGTTGGGGGCATT[-/A]ATGAGAGGAGAGAAA	54813
rs768715321	snp	C/T	5.56571e-05	0.00527498	intron-variant	FAM179B	GRCh38.p7	14:44964475	TAGAGCAGGTATGCT[C/T]CTCTAATTTTCTTGA	54813
rs768793257	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44965561	TTTAGGAAAATATTA[C/T]ATAGGAGATACATAT	54813
rs768808809	snp	C/G	1.64914e-05	0.00287149	missense, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929089	GCTGAATCCAGCCAC[C/G]TATCTGAGATAGGAT	54813
rs768850323	snp	A/G/T	3.29621e-05	0.00405958	missense	KLHL28	GRCh38.p7	14:44945348	AAAACAGTCTCTTCG[A/G/T]TAGCTACATTCAAAC	54813
rs768869143	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44950784	AAGCACTCAGTAATT[G/T]GTAGACGTTATTTAT	54813
rs768989088	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44972280	TGTGTGTGTGTTTTT[C/T]TTTTGCGATAGAACG	54813
rs769010603	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44976633	TAATCAACCTTTACC[C/T]TTAAAAAAAAACTCT	54813
rs769078695	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44977422	TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCACC	54813
rs769129820	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44979669	GTGGCAGAGCTGATT[G/T]GAATGTAGGCAAAAT	54813
rs769131163	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44941349	TGAAATTACCCACCA[A/C]GGCCAGGCACGGTGG	54813
rs769178934	snp	C/G	3.40489e-05	0.00412593	synonymous-codon	KLHL28	GRCh38.p7	14:44934126	ATACCTGTTCATGTG[C/G]GCAGGACCATACCCA	54813
rs769197019	snp	A/C	1.64822e-05	0.00287068	missense	KLHL28	GRCh38.p7	14:44934290	CATAACCACCTAAGG[A/C]ATAAAGTTCTCCTGC	54813
rs769225994	snp	C/T	1.64827e-05	0.00287073	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962981	CTCAACTAGTTGTCT[C/T]GTTACGGGAAGAGAA	54813
rs769248611	snp	G/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927501	TCAAGGAAAAGAAAA[G/T]CAAATGACTACAGTT	54813
rs769320188	snp	A/G	1.71408e-05	0.00292747	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962791	GCTTTGCCGCGGCGG[A/G]GCGGTCGACTTGGCT	54813
rs769357310	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44929913	CTACAGGAAAATGGA[A/G]TATATATCTTTCCAT	54813
rs769366595	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44968415	CAGGCACCCGCCACC[A/C]TGCCCAGTATTTTTA	54813
rs769412696	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44937057	CATCTGAAGTAGGAA[-/C]CAGTCTAGGACTGAG	54813
rs769468354	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44969398	ACTCAAGCGATTGCC[A/C]ACCTTGGCCTCCTAA	54813
rs769489108	snp	A/G	3.29533e-05	0.00405901	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964072	ACCAGCATCCTTTTT[A/G]AAGCTGTGGATACAG	54813
rs769555528	snp	A/G	3.32784e-05	0.00407898	missense	KLHL28	GRCh38.p7	14:44945909	TTAGCAAGCATGTAG[A/G]TCGGGGATGTGTGGT	54813
rs769636056	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44934778	GAGTGTAAACTTGTA[C/T]AAATTACTCTGGAAA	54813
rs769649759	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44973657	TAATTTTCCTTTTCT[C/G]TGAAAAACTTCAATG	54813
rs769794179	snp	A/G	1.65288e-05	0.00287474	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963498	GCTGCATTCACGATT[A/G]TTGGATCAGGAAGAC	54813
rs769840369	snp	C/T	1.65463e-05	0.00287626	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963673	GGCACACTTGAAGTC[C/T]TGCATTTACTGGTTA	54813
rs769880986	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44949091	CAGACTAAACAATTA[C/T]GTTTCAAGATATTTA	54813
rs769883842	snp	A/G	1.64933e-05	0.00287165	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963376	CAGTTTGGAAGTCAG[A/G]TTCCTTATTATTTGG	54813
rs769924502	snp	C/G/T	1.64741e-05	0.00286998	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963037	CAGATCCTTCATATA[C/G/T]GTCTGAAACGTAGTC	54813
rs769944355	snp	G/T	1.67365e-05	0.00289275	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962531	AGACCGATGATAGTC[G/T]AGTTGGGGGCATTAT	54813
rs769956136	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926361	AGTCTTCATCAAGAT[A/G]AAATTTAGATTTTTC	54813
rs769977958	snp	A/G	2.03345e-05	0.00318855	intron-variant	KLHL28	GRCh38.p7	14:44931313	CCTTACATGTTTAGA[A/G]ATTAATAAATTCTTA	54813
rs770018414	snp	C/G	1.64787e-05	0.00287038	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962992	GTCTCGTTACGGGAA[C/G]AGAATCCAGCCCTGC	54813
rs770029973	snp	A/G			synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964380	GGTATTAAGTGCAGG[A/G]AAAGGAAAAAATAAA	54813
rs770033913	snp	C/T	1.79008e-05	0.00299167	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962474	CCTTTCCAGTCCTCT[C/T]TACCTATCGGCTCCA	54813
rs770064132	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44947814	GCCACTTTCCAGCTG[C/G]TAACAGCCTCCACTG	54813
rs770077919	in-del	-/A			intron-variant	KLHL28	GRCh38.p7	14:44935971	ATAATGTAACAGCAT[-/A]AAAAAAAGTCCTCCA	54813
rs770110930	snp	C/T	1.64738e-05	0.00286995	stop-gained, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964171	CCAAGGCTCACAGAG[C/T]AGGGATTTGTGGAAT	54813
rs770250442	snp	C/T	1.71722e-05	0.00293016	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962808	CGGTCGACTTGGCTT[C/T]CCCCGACGCAAGGAA	54813
rs770261481	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44976269	CTACATTTAACCTAT[G/T]GATTTTCTGGCCTTA	54813
rs770352890	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44953574	CACACTCACAGCCCC[C/T]TCACCATGTGAGGCC	54813
rs770354783	snp	C/T	1.64887e-05	0.00287125	missense	KLHL28	GRCh38.p7	14:44945504	TATGTTTCTGCAAAA[C/T]GAGAAATTCCAATAC	54813
rs770373257	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44941164	TCTCTTCAAGAACAA[A/T]ATAAAACCAAACAAA	54813
rs770383293	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44973663	TCCTTTTCTCTGAAA[A/G]ACTTCAATGTTTCTT	54813
rs770419173	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958738	GACAGGCGTCTAAGT[C/T]ACATAATTAATCCCT	54813
rs770460674	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44941288	TTACTTTGTATTCAC[C/T]TCTAGGCCCACTGTA	54813
rs770477179	in-del	-/A			intron-variant	KLHL28	GRCh38.p7	14:44932245	AAAGAAGAGGAAGAG[-/A]GGGGTGGGGGGTGGG	54813
rs770519154	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44929647	TCTCCTGTGGGTATG[A/G]GGGGCCTACTGGAGC	54813
rs770571966	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44944334	TGTTCATTCACTTAT[A/G]TATTATCTATGGCTG	54813
rs770576207	snp	C/T	9.88826e-05	0.00703076	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964308	TCACTGTGGTGACCA[C/T]GTGAGGGATAGCATG	54813
rs770595492	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44979397	TATGGGGTGGAAGGG[A/G]CAAACAAGCTCCCAC	54813
rs770600665	snp	A/G	1.64754e-05	0.00287009	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963018	CCTGCGGAAAGATGC[A/G]CTGCAGATCCTTCAT	54813
rs770700911	snp	C/G	1.64868e-05	0.00287109	synonymous-codon, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929070	GCGACAGTATATCAT[C/G]CCAGCTGAATCCAGC	54813
rs770738996	snp	A/C	1.65359e-05	0.00287536	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963512	TATTGGATCAGGAAG[A/C]CTATAAGAACCGGAC	54813
rs770740229	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44973606	TCTCTCTATATATAC[A/G]TATATATATATCTCT	54813
rs770867494	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44957141	ATTGAAATATTTGTA[A/G]ATGAAATAATATGTT	54813
rs770897206	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44966188	AATTTTTAAATTACA[A/G]AGGCCAGGCAGGGTG	54813
rs770903197	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44930923	ATCAACTATACCCCC[-/T]GGGGAAGAAAGAACA	54813
rs770910552	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44936721	CATGGCCTAAGTGGA[G/T]AATTGAATTTAACTA	54813
rs770939463	snp	C/T	1.84814e-05	0.00303979	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962449	CCCTCCGCGCTGCTT[C/T]TGCTGCCGCCCTTTC	54813
rs771024590	snp	A/G	3.49806e-05	0.004182	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962489	CTACCTATCGGCTCC[A/G]GAGCCGCAGTCGTCC	54813
rs771027271	snp	C/T	5.64913e-05	0.00531436	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962408	TTCCAACCACCACCA[C/T]CTGACAACCCTGCAT	54813
rs771032973	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924707	AGGCATTATCATCCA[A/G]TTCTTTAACTTCACT	54813
rs771077354	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44976235	CACAAAAATTGCCCT[A/G]TCCTTATTCGTTGCC	54813
rs771077799	snp	C/G	1.65638e-05	0.00287778	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962683	TCTGAGTCTGGAGGC[C/G]GTTTGTCAGGGGGAG	54813
rs771086394	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44939821	CTATTCACGGCAATC[G/T]AGGCTTCTTCCAGAC	54813
rs771100518	snp	A/G	1.64996e-05	0.0028722	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963787	ATCAAACAAGAATAC[A/G]TGAAAATCTTCCTCA	54813
rs771160780	snp	C/T	1.72454e-05	0.00293639	missense	KLHL28	GRCh38.p7	14:44934533	AACCAATCCAAGAGT[C/T]ATTCTGAGGAAAGTA	54813
rs771166670	in-del	-/G	1.74906e-05	0.0029572	upstream-variant-2KB, frameshift-variant, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962489	TACCTATCGGCTCCA[-/G]GAGCCGCAGTCGTCC	54813
rs771171707	snp	A/G	4.94662e-05	0.00497299	synonymous-codon	KLHL28	GRCh38.p7	14:44945524	AATTCCAATACAATT[A/G]CCAGGATCAAGTTGG	54813
rs771198162	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44951222	AAGAGAAACTGTCTC[A/C]TGACACACTTGTAGG	54813
rs771204887	snp	A/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961645	CTGTCCTGATAAGCA[A/G]ATGGCAAGAGGAAAG	54813
rs771276881	in-del	-/TAA			intron-variant	FAM179B	GRCh38.p7	14:44979173	CCTATAAGTCACCAT[-/TAA]TAATAATAATAATAA	54813
rs771296283	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44938993	TGCCCCCTGTGCTAT[C/G]TGCAACACTCTTACA	54813
rs771322360	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44931220	AAGTCTTTTTTTTTT[C/T]TTTTCTGGACAAGTA	54813
rs771495160	snp	C/T	0.000164802	0.00907599	synonymous-codon	KLHL28	GRCh38.p7	14:44945656	CCCTGTATAGGCATA[C/T]TCCACAATGGCCTGG	54813
rs771549070	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963138	AGCACTACTGCTTCC[C/T]ATCTTGCTTACTACT	54813
rs771549917	snp	A/C	1.64814e-05	0.00287061	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964321	CACGTGAGGGATAGC[A/C]TGCACATTTATGGAT	54813
rs771635291	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44971991	AGAGGAAGGAGTCAC[A/G]TCTTACATGGCCGGA	54813
rs771672337	in-del	-/AC			intron-variant	KLHL28	GRCh38.p7	14:44948384	ACATATCAGTGAAGA[-/AC]ACAGACTTTGGAAAT	54813
rs771707788	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942792	CTCTTCCCTAAATCC[C/T]CCAGATGGGATAAAT	54813
rs771723114	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44956481	AAGTCAAGCAAATTA[A/C]ACTACAGCCAATTCT	54813
rs771734756	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44938523	ACTACAGGCGCCCAC[A/C]ACCACGCCCAGCTAA	54813
rs771821360	snp	C/T	1.87986e-05	0.00306577	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962416	ACCACCACCTGACAA[C/T]CCTGCATGGCGGCTG	54813
rs771871138	snp	C/T	1.83249e-05	0.0030269	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962456	CGCTGCTTCTGCTGC[C/T]GCCCTTTCCAGTCCT	54813
rs771896335	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940872	CTTGGGAGGCTGAGG[C/T]GGGTGGATCACAAGG	54813
rs771974183	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44970733	CCTAGTTTGCTGAGA[A/G]TTTTCATCATATATG	54813
rs772013911	snp	A/G	1.70179e-05	0.00291696	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962772	CTTCCAGGCTTTGCA[A/G]GCTGCTTTGCCGCGG	54813
rs772033563	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44959481	TTCTTAATAGTTTAC[A/G]GAATTCACACTGACG	54813
rs772061790	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44947682	AGCACTTCATTCTTA[C/T]ACATTTTTAAGTGGA	54813
rs772096745	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44935023	ATGCATACATATATG[A/T]CCAAGAGTGTTTACT	54813
rs772139805	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962234	AGCTGTGGGGTCTAG[A/G]GCTCAGACGGGGGCC	54813
rs772142849	in-del	-/GT			intron-variant	FAM179B	GRCh38.p7	14:44980039	GGATAACCTTATTTA[-/GT]GTAGCTGAAGCTGGC	54813
rs772153504	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44948968	TTAACAAGGAGAATG[A/G]TAGACTAAAAAGTGA	54813
rs772157986	snp	C/T	1.6483e-05	0.00287076	missense	KLHL28	GRCh38.p7	14:44934371	AAGTCCAAGTATTTG[C/T]ATCAGGATTCCAGCA	54813
rs772163372	snp	A/G	1.64811e-05	0.00287059	missense	KLHL28	GRCh38.p7	14:44945105	CAGCGAGGTCGTGTC[A/G]TCAAGACTGTCTGAT	54813
rs772207789	snp	A/T	1.64852e-05	0.00287094	missense	KLHL28	GRCh38.p7	14:44945188	ATGTTTACAAGTGCG[A/T]TCATCACGAATAAGA	54813
rs772213347	in-del	-/CT			intron-variant	KLHL28	GRCh38.p7	14:44942240	ATCTTGGATTCCTCC[-/CT]CTTCCTCATCATCCC	54813
rs772251190	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44952157	GAGCCACTGAGCATG[A/T]CCAAATTAAATCTTA	54813
rs772255568	snp	A/G	1.658e-05	0.00287919	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962694	AGGCGGTTTGTCAGG[A/G]GGAGATGAAGAGGAC	54813
rs772297212	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44938735	CTACTTCCTGGATAC[A/G]CTGGGGCAGGAGTTG	54813
rs772314246	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44929341	ATACAGTAGTCCTCC[C/G]TTTATCTGAGTTTTT	54813
rs772316480	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44977603	ACAGAGAAATTTTAA[A/G]TATGTTGGCCTTAAA	54813
rs772320481	snp	A/G	1.65097e-05	0.00287308	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931484	AAAGTGAATCCTTTT[A/G]TCTGCCATGGATGCA	54813
rs772435898	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44947786	AAGTCAGTTAATAAA[C/T]TATGTTAATATGGCC	54813
rs772478616	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44965675	GATGCTTAATTTTAC[C/T]GTTTGGATAAGGTGG	54813
rs772495831	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44978238	AGTTAGTTTTCTCCT[C/T]TCCTCCCAAATTCCA	54813
rs772544177	snp	C/G	3.29652e-05	0.00405974	missense	KLHL28	GRCh38.p7	14:44934235	CATTTTCTTATTTTG[C/G]GAATGTACTTCTCTA	54813
rs772600397	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44967505	TAAATTAAGTCTTTT[A/G]TCTATGTAATTATTA	54813
rs772657967	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44956754	TTGGAAATTTACACA[C/T]TGACTGGATTATTAA	54813
rs772710415	snp	A/G/T	3.29686e-05	0.00405998	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963904	GTGGTGAACATTTGC[A/G/T]TCTGCTCCCTGCTGA	54813
rs772734473	snp	A/G	1.71634e-05	0.0029294	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962818	GGCTTCCCCCGACGC[A/G]AGGAAGCTTTGTATC	54813
rs772740211	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927783	GAAATGTACAAAGTA[A/G]TGCATAACTGCCTAG	54813
rs772815073	snp	A/C	1.69833e-05	0.00291399	missense	KLHL28	GRCh38.p7	14:44934128	ACCTGTTCATGTGGG[A/C]AGGACCATACCCACC	54813
rs772846025	snp	G/T	1.64741e-05	0.00286998	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964189	GGATTTGTGGAATAT[G/T]CAGTACTGATGCCAT	54813
rs772870442	in-del	-/GTT	9.89054e-05	0.00703157	upstream-variant-2KB, cds-indel, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962974	CTTTTGCCTCAACTA[-/GTT]GTCTCGTTACGGGAA	54813
rs772903070	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942836	GTTTCTATAAAACTA[C/T]CTTGATCGTTGCATA	54813
rs772909270	in-del	-/A			intron-variant	KLHL28	GRCh38.p7	14:44954303	AAAAATTACACTGGC[-/A]AAAAATGTATAAAGA	54813
rs772957760	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44969873	CATGTGGGTCTTTTT[C/G]TGGGCTCTTTACTCT	54813
rs773031890	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961266	AAGGCTGCAGAGACG[C/T]TTGAGGATCCTGCAG	54813
rs773064260	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44977458	AGCTGGGATGGTCTT[C/G]ATCTCCTGACCTCAT	54813
rs773072288	snp	A/G	1.64806e-05	0.00287054	missense	KLHL28	GRCh38.p7	14:44945762	TTGAAATACGGGCTG[A/G]CGCTGGCAAGTACCA	54813
rs773074501	snp	C/T	3.29799e-05	0.00406065	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963384	AAGTCAGGTTCCTTA[C/T]TATTTGGAACTTGAA	54813
rs773081244	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44970952	CTAATATTTTGTTGA[G/T]GATTTTCACATGTTT	54813
rs773136519	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44974274	ATACTTTCCCCAGCT[A/G]TGTCCAGTTTACTAA	54813
rs773208960	snp	A/C	7.13521e-05	0.00597252	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962477	TTCCAGTCCTCTCTA[A/C]CTATCGGCTCCAGAG	54813
rs773212302	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927038	GATTTATTCAAATCA[A/G]TGAAAAAGTTATTGC	54813
rs773400507	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44949325	AAATAATAAGACATG[C/T]TACAGACTAGGTTTG	54813
rs773409714	snp	A/G	1.6698e-05	0.00288941	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962540	ATAGTCGAGTTGGGG[A/G]CATTATGAGAGGAGA	54813
rs773461866	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44964797	CAGATAAAGAGCTAA[A/G]TTCTGGGAATGAAGA	54813
rs773488178	snp	A/G	1.87264e-05	0.00305988	intron-variant	KLHL28	GRCh38.p7	14:44931322	TTTAGAAATTAATAA[A/G]TTCTTATTACCTGTT	54813
rs773572757	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44948091	AAAAAGTTAAAATCT[A/G]GACTTAAAAGTAAAG	54813
rs773582765	snp	C/T	3.2963e-05	0.00405961	missense	KLHL28	GRCh38.p7	14:44945385	TGGAAACAATTTCAT[C/T]CAAGTCAGCATGTGT	54813
rs773585313	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44965678	GCTTAATTTTACTGT[G/T]TGGATAAGGTGGTAA	54813
rs773674932	snp	A/C	1.64765e-05	0.00287019	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963004	GAAGAGAATCCAGCC[A/C]TGCGGAAAGATGCGC	54813
rs773675390	snp	C/G	1.65701e-05	0.00287833	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963549	CGTCGAAGAACTAAA[C/G]CAGGTGCTGGGAAAA	54813
rs773724827	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44978389	GTATGACATATATAT[A/G]AAAATGAGATTTTTG	54813
rs773795872	snp	G/T	1.64749e-05	0.00287005	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963021	GCGGAAAGATGCGCT[G/T]CAGATCCTTCATATA	54813
rs773812453	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44970687	TTTCTTGTAGTGTTC[A/G]CTATAAAGTTGAGAA	54813
rs773866152	snp	A/G	1.65037e-05	0.00287256	synonymous-codon, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929133	TGTATTCAGATAGGA[A/G]GACCCTGAGTGACCA	54813
rs773873166	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44954196	GGAATAGAAAATGAT[A/G]CAAAACCTCTGGAGG	54813
rs773874639	snp	C/T	6.59239e-05	0.00574087	synonymous-codon	KLHL28	GRCh38.p7	14:44945404	GTCAGCATGTGTAAG[C/T]TCAAAAAACTCTTCA	54813
rs773924088	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44955554	GCTAAGGTGGGAGGA[C/T]AGCTTGAGCCCAGGA	54813
rs773990159	snp	G/T	1.64741e-05	0.00286998	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963118	GCCCGACTTAGAGCT[G/T]CCACAGCACTACTGC	54813
rs774037502	snp	A/G	1.65381e-05	0.00287555	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963515	TGGATCAGGAAGACT[A/G]TAAGAACCGGACCCA	54813
rs774045525	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44969172	CTTTTCTTTCTTTTC[-/T]TTTTTTTTTTTTTGT	54813
rs774045666	snp	A/G	3.29647e-05	0.00405971	synonymous-codon	KLHL28	GRCh38.p7	14:44934363	CTCTAGAGAAGTCCA[A/G]GTATTTGTATCAGGA	54813
rs774140753	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44952628	AACCTCAAACTCCTA[A/G]GCTCAAGTGACCTAC	54813
rs774206099	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44931928	AATGAGGATAGTGCA[A/C]CCTGAAGGGATTCAT	54813
rs774208842	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44938314	CCAAAAGGGAGAAAA[A/G]GGAAATACAAAGAGT	54813
rs774242899	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44958730	CATGTTATGACAGGC[A/G]TCTAAGTTACATAAT	54813
rs774248262	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44946120	ATCACATCATTCAAC[C/T]TATTTATTATAGATA	54813
rs774311898	snp	C/G	1.67913e-05	0.00289748	missense	KLHL28	GRCh38.p7	14:44945923	GGTCGGGGATGTGTG[C/G]TCCATCTACAGAAAA	54813
rs774341703	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44933455	TATTAGGATTACAGG[C/T]GTGAACCACCACACC	54813
rs774371763	snp	G/T	1.73033e-05	0.00294132	missense	KLHL28	GRCh38.p7	14:44934538	ATCCAAGAGTCATTC[G/T]GAGGAAAGTACATCT	54813
rs774374029	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44950790	TCAGTAATTGGTAGA[C/T]GTTATTTATTTTTAC	54813
rs774374174	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44935353	CATACTCTGTTTCTT[G/T]AACTGGTTTGTAATG	54813
rs774417497	in-del	-/TAAAC			intron-variant	KLHL28	GRCh38.p7	14:44956609	AAAAATCTTGTAAAA[-/TAAAC]TAAATTCTTCAACAA	54813
rs774419924	snp	A/G	3.29647e-05	0.00405971	missense	KLHL28	GRCh38.p7	14:44934253	ATGTACTTCTCTACA[A/G]ATTGTAAATAAGATT	54813
rs774425592	snp	G/T	1.65701e-05	0.00287833	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962688	GTCTGGAGGCGGTTT[G/T]TCAGGGGGAGATGAA	54813
rs774426966	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44949271	GTGAATACCGATAAG[A/G]AGATGTAGAGATCTT	54813
rs774547159	snp	A/G	3.35289e-05	0.0040943	synonymous-codon	KLHL28	GRCh38.p7	14:44945041	TTACCTATCCAAACA[A/G]GCAAAGAGTCCAGAT	54813
rs774550576	snp	A/G/T			missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963256	GAGACAGCTTTCTCC[A/G/T]CACTTCAACAAATTG	54813
rs774600729	snp	A/G	1.88727e-05	0.00307181	intron-variant	FAM179B	GRCh38.p7	14:44964500	TCTTGAGTCGAAAGT[A/G]TGAAGAATTTAAATG	54813
rs774605426	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44976676	TGAAATGTGATGTTA[C/T]TAAATGTTTTAAACT	54813
rs774623890	in-del	-/AAT			intron-variant	KLHL28	GRCh38.p7	14:44959079	AGGATTGAAAGAAAA[-/AAT]AATAAATTAAAAAAT	54813
rs774632076	snp	C/T	4.95413e-05	0.00497677	missense, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929153	CTGAGTGACCACCGA[C/T]GACATAAAGGTAGTT	54813
rs774649614	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44941831	ACTTGGTTCCCCTAC[C/T]GCTAAAATTGTTCCT	54813
rs774657428	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44976724	ATGTGTATAGTCAAT[A/G]AGACCAGCACATGAT	54813
rs774719524	snp	A/G	0.000380156	0.0137816	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963685	GTCCTGCATTTACTG[A/G]TTATTCGCCTTGGAG	54813
rs774739030	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44938538	ACCACGCCCAGCTAA[-/T]TTTTTGTATTTTTAG	54813
rs774792031	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926697	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	54813
rs774799569	snp	C/G/T	3.30116e-05	0.00406262	missense, stop-gained, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963265	TTCTCCGCACTTCAA[C/G/T]AAATTGGGGAGCGAC	54813
rs774810800	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44944682	TATCTTCTGATATAA[C/T]TGACAATAATAAATC	54813
rs774829937	snp	G/T	1.64901e-05	0.00287137	missense	KLHL28	GRCh38.p7	14:44945528	CCAATACAATTACCA[G/T]GATCAAGTTGGCTTT	54813
rs774997297	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44931692	GCTTAGGTTTTGCTG[A/G]TAAGATTGCAAAGAT	54813
rs775010134	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44967475	ACAGTCAGAATTTTG[C/T]GGTCAAACTTTTCTT	54813
rs775036435	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44968422	CCGCCACCATGCCCA[A/G]TATTTTTAGTAGAGA	54813
rs775067293	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44969443	AGGTGCAAGCTACCA[C/T]GCCTGGCCTATCAGA	54813
rs775089477	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44979836	TCTTGACAGGAGCTA[A/G]GGCTTCAAATGGTCA	54813
rs775091625	snp	C/G/T	0.000181207	0.00951697	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963140	CACTACTGCTTCCCA[C/G/T]CTTGCTTACTACTGA	54813
rs775108364	snp	C/T	1.64833e-05	0.00287078	missense	KLHL28	GRCh38.p7	14:44934374	TCCAAGTATTTGTAT[C/T]AGGATTCCAGCATTC	54813
rs775222350	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44932173	GACTAAAGGTACATG[A/C]CCCCATGCCTGGCTT	54813
rs775238820	in-del	-/A			intron-variant	KLHL28	GRCh38.p7	14:44949983	ATCTAAACAGACTGT[-/A]ACACCTGATGAACAG	54813
rs775344401	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44952550	TTTTTAGAGACAGGA[G/T]CTCACTATGTTGCCC	54813
rs775354219	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44978859	AGCCAGGCATGGTGG[C/T]ATATACCTATAGGCC	54813
rs775404922	in-del	-/CAGA			intron-variant	FAM179B	GRCh38.p7	14:44970468	TTGAGACTTTCTATG[-/CAGA]CAATCATGTCATCTG	54813
rs775406625	snp	C/T	1.64833e-05	0.00287078	synonymous-codon	KLHL28	GRCh38.p7	14:44934258	CTTCTCTACAGATTG[C/T]AAATAAGATTGTCCA	54813
rs775435333	in-del	-/C	3.38951e-05	0.0041166	upstream-variant-2KB, frameshift-variant, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962509	GCAGTCGTCCTTCCG[-/C]CCCCAGAGACCGATG	54813
rs775470225	snp	A/G/T	3.29658e-05	0.00405978	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964331	ATAGCATGCACATTT[A/G/T]TGGATCTTACAGCCC	54813
rs775482623	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44946064	ATACTTCATAGTAAA[C/T]ACTAGAACTAGAGGC	54813
rs775510512	snp	A/T			missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964392	AGGAAAAGGAAAAAA[A/T]AAATTACCATGGGAA	54813
rs775752267	snp	C/G	1.64852e-05	0.00287094	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963401	ATTTGGAACTTGAAG[C/G]CTCTGGATTTCCTGA	54813
rs775764264	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935200	ACACACATAATGTTG[A/G]GATAAAAAAGTCAAA	54813
rs775798503	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44975454	ATTTCCTAAACCACC[G/T]TTCCCCTTTTTTTGT	54813
rs775817853	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44949140	ATTATTGAATCATTA[C/T]CAGTGCCACAGGACT	54813
rs775870563	snp	A/G	4.98641e-05	0.00499295	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962567	GAGAGAAAAACTACT[A/G]CTTCCGTGGAGCTGC	54813
rs775874256	snp	C/T	3.30524e-05	0.00406511	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931496	TTTATCTGCCATGGA[C/T]GCAACCATCTCCCAG	54813
rs775962478	in-del	-/TTC			intron-variant	FAM179B	GRCh38.p7	14:44973836	ATATTCCAATCCACT[-/TTC]TTCTTCTTTGTATGG	54813
rs776031134	snp	G/T	1.64974e-05	0.00287201	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963800	ACATGAAAATCTTCC[G/T]CAAGCTAATGAAGGA	54813
rs776046121	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44976435	ATCACAGTGCTTACT[A/G]TTACAGTGAATTGAA	54813
rs776046499	in-del	-/TC			intron-variant	FAM179B	GRCh38.p7	14:44973580	CTCCAGTGTACTTTC[-/TC]TCTCTCTCTCTCTCT	54813
rs776074722	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44944412	TGGCTCACAAAGTCT[A/G]AAATATTTACTGTTT	54813
rs776079342	in-del	-/TC			intron-variant	FAM179B	GRCh38.p7	14:44973578	TCCTCCAGTGTACTT[-/TC]TCTCTCTCTCTCTCT	54813
rs776135525	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926452	ATAGTGGAGATGATA[C/T]ATGAGTAAAATATTG	54813
rs776141400	snp	C/G	3.31686e-05	0.00407225	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962696	GCGGTTTGTCAGGGG[C/G]AGATGAAGAGGACAC	54813
rs776203091	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44979561	TTATTCAGACTATTG[C/T]AGCAGCTAACTCTTA	54813
rs776233602	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963162	TACTACTGAGGACTT[A/G]TTGCTTGGTCTGGAT	54813
rs776251161	snp	C/T	3.2962e-05	0.00405954	missense	KLHL28	GRCh38.p7	14:44945709	GAAACTCAACCTCAC[C/T]GTTCTCTTTTTCAGA	54813
rs776277815	snp	C/T	7.73141e-05	0.006217	intron-variant	KLHL28	GRCh38.p7	14:44934091	ATCCATAAACATATG[C/T]AATTTAATTATTAAG	54813
rs776288837	in-del	-/T	1.70726e-05	0.00292164	upstream-variant-2KB, frameshift-variant, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962852	CACTGGGCCGAGTGC[-/T]TGTGGAAGGAGGTAG	54813
rs776358358	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927285	TTTATGGAAGAACAA[A/G]GAACTGTAAATTGCC	54813
rs776362751	snp	G/T			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960205	CCCAGGAAAAGGGCA[G/T]GATAACTGCTTAAGT	54813
rs776448491	snp	G/T	1.69063e-05	0.00290738	synonymous-codon	KLHL28	GRCh38.p7	14:44934507	ATAGCGAGGAATGTT[G/T]AGGGGTGCCAAACCA	54813
rs776505492	snp	A/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924851	AAAGACATATGGATA[A/T]CAATTTTTCTCTCTG	54813
rs776506538	snp	G/T	1.87043e-05	0.00305808	intron-variant	FAM179B	GRCh38.p7	14:44964488	CTTCTCTAATTTTCT[G/T]GAGTCGAAAGTGTGA	54813
rs776540247	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44942909	TGAACTTGTTGAAGG[G/T]CAATTATCTAGCAGT	54813
rs776602927	snp	A/G	1.64939e-05	0.0028717	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964348	GGATCTTACAGCCCA[A/G]CTATCTGTACCCGAA	54813
rs776623041	snp	A/G	1.65075e-05	0.00287289	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963272	CACTTCAACAAATTG[A/G]GGAGCGACTTGGCCA	54813
rs776624344	snp	A/T	1.662e-05	0.00288266	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928980	GCCATCCGGATGTTC[A/T]TGCAGTACAAGTTTC	54813
rs776723464	snp	C/G	4.94792e-05	0.00497365	missense, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929093	AATCCAGCCACGTAT[C/G]TGAGATAGGATCATA	54813
rs776761323	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44946447	TGAATTTAATGAAGG[A/T]ACTATTACCACCAAT	54813
rs776832508	snp	A/G	1.65748e-05	0.00287874	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963658	TTCAAAGTGGTGCAT[A/G]GCACACTTGAAGTCC	54813
rs776959117	snp	A/G			upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962591	GAGCTGCGGGGGACC[A/G]CGGTTCCTGCCCCAC	54813
rs776983352	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44932126	TTCCGGGGCTAAAGT[C/G]ATCTTTCTGCCTCAG	54813
rs776999566	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44951333	GAGAATCACAAGGTG[C/T]GTCAAGCCACGGATA	54813
rs777067042	snp	C/T	1.7154e-05	0.0029286	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962796	GCCGCGGCGGGGCGG[C/T]CGACTTGGCTTCCCC	54813
rs777083417	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44952415	TGGGCAAACTGTGTT[G/T]TAAGTCCTCCAGGTT	54813
rs777138303	snp	A/G/T			intron-variant	FAM179B	GRCh38.p7	14:44968409	GGACTACAGGCACCC[A/G/T]CCACCATGCCCAGTA	54813
rs777151045	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44951245	CTTGTAGGGGAAATA[A/G]AGAGGTGAGTGGAAA	54813
rs777159180	snp	A/C/G	4.98528e-05	0.00499243	upstream-variant-2KB, synonymous-codon, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962706	AGGGGGAGATGAAGA[A/C/G]GACACTCGGCTCCTT	54813
rs777188564	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44974372	CTTCTTAGAAGTAAC[A/G]CTTCATGACTTATAT	54813
rs777263400	snp	C/T	1.64857e-05	0.00287099	missense	KLHL28	GRCh38.p7	14:44945226	CTTCATATAGTCTAG[C/T]GAGAAACTTAACACT	54813
rs777362925	in-del	-/AAT			intron-variant	FAM179B	GRCh38.p7	14:44966475	AGACTGCATCTCAAA[-/AAT]AATAATAATAATACT	54813
rs777387035	snp	C/T			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960686	ATATTTACACAGCCT[C/T]ATTTACATTATAGTC	54813
rs777401891	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44944112	AAATGGTCAGAAATC[C/T]ACAGTATTAAAAAAT	54813
rs777463441	snp	A/G	1.88432e-05	0.00306941	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962404	TTTCTTCCAACCACC[A/G]CCACCTGACAACCCT	54813
rs777475831	snp	C/T	1.66087e-05	0.00288168	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963617	GCTTCATTAGTTTGC[C/T]ATATAATTTGTTAGA	54813
rs777498828	snp	A/G	1.64825e-05	0.00287071	synonymous-codon	KLHL28	GRCh38.p7	14:44945325	TGATCCAAGACTCTA[A/G]TGCATAAAAAACAGT	54813
rs777556961	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44946169	AAAGGTTACATGAGA[C/T]GCCCCAAACCAAAAA	54813
rs777579434	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44965109	TCTATATTTACCAGT[G/T]GTAACATCTTGACAT	54813
rs777585997	snp	A/G	1.70918e-05	0.00292329	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962501	TCCAGAGCCGCAGTC[A/G]TCCTTCCGCCCCAGA	54813
rs777663506	snp	C/T	1.64904e-05	0.00287139	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962961	CTTTAGCTTAGCACT[C/T]TTGCCTCAACTAGTT	54813
rs777694867	snp	A/T	1.64879e-05	0.00287118	synonymous-codon, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929037	CATTTGTCAAAGTGC[A/T]GTTAACCCAAAGTTG	54813
rs777695016	snp	A/C			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962321	GTTCTTTTGCCTCTT[A/C]TGCAGCTTGGGGCTT	54813
rs777810693	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44950394	GTATTGACTAGATTC[A/G]TTTTTAATATAATTA	54813
rs777830587	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44941051	GTTGCTGTGAGTTGA[C/G]ATGATGCCAATACAT	54813
rs777839421	snp	G/T	6.61179e-05	0.00574931	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963500	TGCATTCACGATTAT[G/T]GGATCAGGAAGACTA	54813
rs777845816	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44936649	AAGGCTCCATGTGAG[A/G]CAAGTTAAAATGGGT	54813
rs777849210	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44953262	GGAAACAGGTAAAAC[G/T]AGATTTCTGCTACAT	54813
rs777885504	in-del	-/TCC/TCCC			intron-variant	FAM179B	GRCh38.p7	14:44969147	CCTTCCTTCCTTCCT[-/TCC/TCCC]TTCTTTCTTTCTTTT	54813
rs777944814	snp	G/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924585	TCACATTCTTTGCAA[G/T]AGAGTACAAATATTA	54813
rs777956038	snp	C/G	1.65002e-05	0.00287225	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931436	ATTATGTCCACCCAC[C/G]ACAAAAATAAAGCCT	54813
rs778032114	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44933806	GATAATTTACATACT[A/G]TGCACATAGATGTAC	54813
rs778068577	snp	A/G	1.64895e-05	0.00287132	missense	KLHL28	GRCh38.p7	14:44934442	CGCACATTAGTTGCA[A/G]TACCACCTATAACAT	54813
rs778070330	snp	A/G/T	5.15675e-05	0.00507755	missense, stop-gained, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964411	TTACCATGGGAAAAT[A/G/T]AGCAACCTGGAATCA	54813
rs778081400	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44939797	CTCACCAGAATCACC[C/T]TTAACATTCTATTCA	54813
rs778102210	in-del	-/CTC	1.65974e-05	0.0028807	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963581	TTAACCCTAGTTCTA[-/CTC]CTCATTCTAGTCTTG	54813
rs778144755	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44929554	TATCATAGATATATA[C/T]GTATAGGAAAAAATA	54813
rs778149350	snp	A/T	0.000156015	0.00883082	intron-variant	KLHL28	GRCh38.p7	14:44931554	ACACTGCAAATATTT[A/T]AAAAAAATTTAATTT	54813
rs778152625	snp	A/G	1.64887e-05	0.00287125	synonymous-codon	KLHL28	GRCh38.p7	14:44945515	AAAACGAGAAATTCC[A/G]ATACAATTACCAGGA	54813
rs778192195	in-del	-/AA	1.73898e-05	0.00294866	intron-variant	KLHL28	GRCh38.p7	14:44945950	AAAATAAAAAAGCAT[-/AA]AGACAGTTATTTCAA	54813
rs778232096	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44934983	TTATGTGTCCTGTCT[C/G]AGCAACTCTACTGAT	54813
rs778239241	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44979350	CAGTTAAGGCTCTCT[C/G]CTTCATAGACAGCAC	54813
rs778304110	in-del	-/G			intron-variant	KLHL28	GRCh38.p7	14:44936479	GTGTTGGGAAGATGA[-/G]GTAGTTCTCTTCTGG	54813
rs778337728	snp	A/G	1.64819e-05	0.00287066	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964319	ACCACGTGAGGGATA[A/G]CATGCACATTTATGG	54813
rs778355251	snp	C/G	1.64923e-05	0.00287156	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963239	AGACAGAAGAAGAAT[C/G]TGAGACAGCTTTCTC	54813
rs778415538	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925741	TTGATACCACTTCCT[A/G]TAATTTAATATTCAC	54813
rs778472295	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44967988	TGAGATGTCAGTGTA[C/T]ATATTATTAAAAAGA	54813
rs778519316	snp	C/T	1.65048e-05	0.00287265	missense	KLHL28	GRCh38.p7	14:44934463	CCTATAACATATACT[C/T]TTTGGTCTAAAACGC	54813
rs778532162	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44973514	ATGATTTTCTGTTAG[A/G]TCTGTTAAAAATATG	54813
rs778534218	snp	C/T	1.7406e-05	0.00295003	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964425	TGAGCAACCTGGAAT[C/T]ATGGGAGAAAACCAG	54813
rs778642789	in-del	-/CT			intron-variant	KLHL28	GRCh38.p7	14:44948339	TGTACTACAGTAGTA[-/CT]ATGGTAGCAGTGAGG	54813
rs778706373	snp	A/C	4.95176e-05	0.00497558	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963726	GCAGTTCTTGGGACC[A/C]GTTATAGCAGCTTCT	54813
rs778706808	snp	C/G	1.65976e-05	0.00288072	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963638	ATTTGTTAGACGATT[C/G]TAACTTCAAAGTGGT	54813
rs778740643	snp	C/T					GRCh38.p7	14:44926120	TCAGCAGAGTGTTCA[C/T]AATGAAACTTCTCAC	54813
rs778744008	snp	A/G					GRCh38.p7	14:44936246	GCAGAGAAAGACCAT[A/G]GGACCAGAGGGGATT	54813
rs778747464	snp	C/T	1.77241e-05	0.00297686			GRCh38.p7	14:44929243	TAACCATGAAGTATA[C/T]TTTTTCTCACTAAAA	54813
rs778770871	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44973254	TCCTTTTTTTTTAAA[G/T]TACTTTTTTTTAGTA	54813
rs778799546	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962353	GAGAGGATCTGGAAG[C/T]CTGGGCTCCATCGAG	54813
rs778807330	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44940820	CTTTACCCTATCCCT[C/G]TTTACTTATCTCTTT	54813
rs778833576	snp	C/G	0.000132457	0.00813701	missense	KLHL28	GRCh38.p7	14:44945466	TGTATTTAGTGGCTG[C/G]CAAATAAAGGTCACG	54813
rs778837162	snp	A/G	9.89968e-05	0.00703481	missense	KLHL28	GRCh38.p7	14:44934172	ATTCCATCCAATACC[A/G]CTGCAGCAAAACAAC	54813
rs778863725	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44965585	TACATATATATTAAG[C/T]AGAAGATAAGTAGTG	54813
rs778888516	in-del	-/C			intron-variant	FAM179B	GRCh38.p7	14:44965295	ATATGTAACAGACAG[-/C]CTGTATTTAAATTTC	54813
rs778991636	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44948809	CTTCCTTTCCTCCAA[C/T]TCAAATTCTCAAAAC	54813
rs778992651	snp	C/G	1.6949e-05	0.00291105	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962757	GGATCCTTCTGAGGC[C/G]TTCCAGGCTTTGCAA	54813
rs779001080	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44967423	TAAGTAAAGTTTAAG[A/G]TTTCGTTACAGTTCT	54813
rs779026601	in-del	-/A			intron-variant	KLHL28	GRCh38.p7	14:44952904	AAGGGTAAGTACCAT[-/A]AAAAAAAAAAAAACA	54813
rs779072932	snp	A/G	1.64822e-05	0.00287068	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963863	TGGAACATCTCAAAC[A/G]TAAGCATTCCAGAGT	54813
rs779088413	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44958411	AAAAAAAATTCAAAC[C/T]GACAGTTTTCTTTAA	54813
rs779092325	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44953093	TAACAGGATTAAATG[A/G]GACGTATGTAAGGAA	54813
rs779104364	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44938707	GGTGAATAATCTCCT[C/T]CGACTCCATGTCCTA	54813
rs779117759	snp	C/G	1.65323e-05	0.00287505	intron-variant	KLHL28	GRCh38.p7	14:44931576	ATTTAATTTACAGAT[C/G]TTTTGTGTCATTCTT	54813
rs779145890	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44952020	CACATCACCACGCCC[A/G]ACTAGTTTTTGTATT	54813
rs779161582	snp	A/G			upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44961986	CAGAGCAAGGAAAGC[A/G]TCACATCCGTCAAAT	54813
rs779203636	in-del	-/TCTTT			intron-variant	FAM179B	GRCh38.p7	14:44969157	TTCCTTTCTTTCTTT[-/TCTTT]CTTTTCTTTCTTTTC	54813
rs779213196	snp	C/T	1.65138e-05	0.00287343	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963329	GTCTGCCCTCTGCCC[C/T]GAGGAGACACTACAA	54813
rs779265707	in-del	-/AG			intron-variant	KLHL28	GRCh38.p7	14:44929706	CTTATAATAAAAGTA[-/AG]AGTTACTGAGGTGAG	54813
rs779271774	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44942731	CTCTGCTTGATTCTT[C/G]CTTAGCATTCAACAC	54813
rs779299119	snp	A/C	4.95127e-05	0.00497533	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963258	GACAGCTTTCTCCGC[A/C]CTTCAACAAATTGGG	54813
rs779348498	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44978048	TAACATGAGATTTTG[A/G]GGATAATTGGTGATT	54813
rs779407331	snp	C/T	1.64887e-05	0.00287125	missense	KLHL28	GRCh38.p7	14:44945832	TGATGTCACAGAGTT[C/T]GTGATGTTGGCGAAG	54813
rs779478382	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44950374	TCTCAAATCAAGGTT[A/T]TGAAGTATTGACTAG	54813
rs779531961	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44929327	ATTATACAGGCAATA[C/T]ACAGTAGTCCTCCCT	54813
rs779727388	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44934867	TTCCTATATATCTAC[A/T]CTTCTGAATGTCTAT	54813
rs779745803	snp	C/T	1.65051e-05	0.00287267	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963353	ACTACAATCGCCGCC[C/T]GGAGTCCCAGTTTGG	54813
rs779769073	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44939714	ATTTCTATCAACATT[C/G]TGATCATGCCCACTT	54813
rs779848068	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44970291	AAATATCCTACTTCT[C/G]TATGTTAATGTAAAT	54813
rs779869465	snp	C/T	1.65034e-05	0.00287253	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963752	CTTCTGTCAAAGTGC[C/T]GGCGGACAACAAGTT	54813
rs779954202	snp	A/C	1.651e-05	0.0028731	missense, intron-variant	KLHL28	GRCh38.p7	14:44931417	TGGACAAATGTGAGA[A/C]TCCATTATGTCCACC	54813
rs779955721	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44975160	TTCCCCTTTCTGTGT[A/T]TGTTTTCATTAGCCA	54813
rs780054236	snp	A/G/T	3.31144e-05	0.00406894	stop-gained, synonymous-codon	KLHL28	GRCh38.p7	14:44934477	TTTTTGGTCTAAAAC[A/G/T]CATATTCCAAATTCA	54813
rs780105520	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44972721	GTTAGCATGGTGTAC[C/G]TTTCTCCATCTCTTT	54813
rs780113338	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44959100	AAATTAAAAAATATA[C/T]AATCAAATGATATAT	54813
rs780124318	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44977329	AAGCTCCACCTTCCG[G/T]GTTCACGCCATTCTC	54813
rs780145499	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44977872	CCAGGCTGGTCTCGA[A/G]CTCCTGAGCTCAAGC	54813
rs780155784	snp	C/T	3.29625e-05	0.00405958	missense	KLHL28	GRCh38.p7	14:44945346	AAAAAACAGTCTCTT[C/T]GGTAGCTACATTCAA	54813
rs780191392	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961156	GTCTACTATCATTCC[C/T]AAATCCACAAGGCAG	54813
rs780223582	snp	G/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927444	AAGAAAAATTATCTT[G/T]CAGAGACTTTATAAG	54813
rs780239717	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44950586	TGCATATATTTGTAT[G/T]ATATGCAGTATAGTT	54813
rs780334342	snp	A/G	1.64749e-05	0.00287005	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964148	CCAGATTGGCTAGGA[A/G]AACCTTACCAAGGCT	54813
rs780346026	snp	C/T	1.8912e-05	0.003075	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962374	CTCCATCGAGCCCTT[C/T]GGAGACGGCAATGGT	54813
rs780347964	snp	C/T	2.04267e-05	0.00319577	intron-variant	KLHL28	GRCh38.p7	14:44934071	TGCTAATGAGACTTT[C/T]AAAAATCCATAAACA	54813
rs780612850	snp	A/C/G	3.29882e-05	0.00406118	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963375	CCAGTTTGGAAGTCA[A/C/G]GTTCCTTATTATTTG	54813
rs780706315	snp	C/T	4.94262e-05	0.00497098	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964034	CTTTTGCCGTATTGG[C/T]ATCATCAATGGGCTC	54813
rs780717814	snp	A/G	1.65288e-05	0.00287474	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929013	CACCATACTATTTCC[A/G]AGAGTTCACATTTGT	54813
rs780753578	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44941230	TCTCCTTCCTGTCTC[C/T]AGCAAGATTCTTAAA	54813
rs780762336	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44958927	CACTCATATACATCA[A/G]GAAAACTGATTCAAT	54813
rs780808572	snp	C/T	1.65162e-05	0.00287365	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963475	AAATTTGGGATTATT[C/T]CTCAGGAGCTGCATT	54813
rs780814097	snp	C/T	0.00011704	0.00764895	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931343	ATTACCTGTTCTAGG[C/T]TCTTTCATTGGTCTA	54813
rs780886257	in-del	-/CCACAAAATTGCTAGA			intron-variant	FAM179B	GRCh38.p7	14:44967367	GTAACCCCCCTCCCC[-/CCACAAAATTGCTAGA]CCAGCAACAGCAACC	54813
rs780914157	snp	C/T	1.68148e-05	0.0028995	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962739	ACTCCTCCGCACTGC[C/T]CGGGATCCTTCTGAG	54813
rs780914256	snp	C/T	8.75373e-05	0.00661521	intron-variant	KLHL28	GRCh38.p7	14:44945006	TCAATTAGCATCATT[C/T]ATTTAGGAAAGCCTT	54813
rs781002055	snp	A/G	1.65649e-05	0.00287788	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962646	CCTCTTGATGCCCTC[A/G]GAGGCAGTCTCAAGC	54813
rs781079331	snp	C/T	1.64751e-05	0.00287007	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963974	TTGATCTTGCCCCAG[C/T]TCTTGTAGATAGCAA	54813
rs781108483	snp	C/T	1.64836e-05	0.0028708	missense	KLHL28	GRCh38.p7	14:44945174	GCTTCATTCAAAAGA[C/T]GTTTACAAGTGCGAT	54813
rs781136933	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44958076	CCATAGTTTTTGTTC[-/T]TTTTTTTTTTTTTTA	54813
rs781205128	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44976238	AAAAATTGCCCTATC[C/T]TTATTCGTTGCCTAT	54813
rs781236683	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927230	ATTAAAAATGATTTT[A/G]CATAGTTTTGTAGTA	54813
rs781237059	in-del	-/T	1.83795e-05	0.0030314	splice-donor-variant	FAM179B	GRCh38.p7	14:44964468	AGGATATAGAGCAGG[-/T]TATGCTTCTCTAATT	54813
rs781251685	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44973609	CTCTATATATACATA[C/T]ATATATATCTCTCTC	54813
rs781261896	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44941100	GTGAGACACCTGGGC[A/G]ACAGAGCGAGATGCC	54813
rs781263117	snp	A/G			synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964098	TACAGTTGAACTGCA[A/G]GATAATGGAGATGGA	54813
rs781341387	snp	A/C	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964159	AGGAAAACCTTACCA[A/C]GGCTCACAGAGCAGG	54813
rs781370816	snp	A/G	4.94613e-05	0.00497275	synonymous-codon	KLHL28	GRCh38.p7	14:44945482	CAAATAAAGGTCACG[A/G]CAACCATATGTTTCT	54813
rs781423286	in-del	-/AA	1.8393e-05	0.00303252	intron-variant	KLHL28	GRCh38.p7	14:44934104	TGCAATTTAATTATT[-/AA]GTTAAATACCTGTTC	54813
rs781458414	snp	A/G	3.29473e-05	0.00405864	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963107	AAAGTACCGATGCCC[A/G]ACTTAGAGCTTCCAC	54813
rs781477749	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44932931	TGCCATCACTTTCTC[A/G]GTCAACAAACCTCAG	54813
rs781495854	snp	C/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926296	AGATTTTCATAATTT[C/G]TTCACTGGTGTATGG	54813
rs781564947	snp	C/T	1.6489e-05	0.00287128	missense	KLHL28	GRCh38.p7	14:44945591	TTTATCTGGAGTAGG[C/T]TTGCTGCTGGCAGGA	54813
rs781600798	snp	C/T	1.64819e-05	0.00287066	synonymous-codon	KLHL28	GRCh38.p7	14:44934225	CACAGGTTGCCATTT[C/T]CTTATTTTGGGAATG	54813
rs781646857	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44969353	AGACGGGATTTCACC[A/G]TGTTGGCCAGGCTGG	54813
rs781649397	in-del	-/TC			intron-variant	FAM179B	GRCh38.p7	14:44969104	GATACCTCATTTCTT[-/TC]TTTCTTTCCTTCCTT	54813
rs781713377	snp	C/T	1.64825e-05	0.00287071	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964278	GGCTGGTAACAGAAC[C/T]CAGAGTGCACACTGT	54813
rs781755919	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926074	TGATCCTTTTTAACA[C/T]AGAAACATGTGGCTT	54813
rs781760393	snp	A/G	1.64798e-05	0.00287047	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962988	AGTTGTCTCGTTACG[A/G]GAAGAGAATCCAGCC	54813
rs781764331	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44954937	CTGAAGTCTCTATTG[C/T]GACATGCCCTAAAAT	54813
rs796253331	multinucleotide-polymorphism	AG/CA			intron-variant	KLHL28	GRCh38.p7	14:44950034	ACAGGTAATGGAACA[AG/CA]GGTACTGAGTCTGGG	54813
rs796335847	snp	G/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961811	CAAAACACTGCCAAA[G/T]CCTGCACCGCTGGAG	54813
rs796476080	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44959535	AAATTTGAGTAAGAA[A/C]ACAGAAAAATCATAG	54813
rs796609250	snp	C/T			intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937633	AGTCCTTATGGTCTT[C/T]TGATGGTGTCTTAGT	54813
rs796753655	snp	C/T			synonymous-codon	KLHL28	GRCh38.p7	14:44945380	GTCATTGGAAACAAT[C/T]TCATCCAAGTCAGCA	54813
rs796832303	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44969336	TTTTGTATTTTTAGT[A/G]GAGACGGGATTTCAC	54813
rs797014057	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44969141	CTTCCTTCCTTCCTT[C/T]CTTCCTTTCTTTCTT	54813

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