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
rs961194	snp	C/T	0.0998734	0.199905	intron-variant	FAM179B	GRCh38.p7	14:44973788	gtatagacttctaaa[C/T]tgatgggtttttttt	54813
rs1115185	snp	A/C	0.339203	0.233544	intron-variant	FAM179B	GRCh38.p7	14:44973596	TCTCTCTCTCTCTCT[A/C]TATATATACATATAT	54813
rs1510518	snp	A/C	0.0217236	0.101931	intron-variant	FAM179B	GRCh38.p7	14:44975345	CTAATACAATCTATT[A/C]ACTTATATTAGACAT	54813
rs1955669	snp	C/G/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926787	tgctgggattacagg[C/G/T]gtgagccactgcgcc	54813
rs1980522	snp	G/T	0	0	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963335	CCTCTGCCCTGAGGA[G/T]ACACTACAATCGCCG	54813
rs2144107	snp	C/T	0	0	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961178	ACAAGGCAGAATTCT[C/T]TTAGAACCATGATGC	54813
rs3036333	in-del	-/TA			intron-variant	FAM179B	GRCh38.p7	14:44973604	CTCTCTCTATATATA[-/TA]CATATATATATATCT	54813
rs3742591	snp	C/G	0.109482	0.206782	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963952	TTTGACTTGCCCAAA[C/G]TGTCCTTTGATCTTG	54813
rs3825629	snp	C/G	0.1839	0.241103	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963667	GTGCATGGCACACTT[C/G]AAGTCCTGCATTTAC	54813
rs6572290	snp	A/G	0.313082	0.241911	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927962	GATGTTAACATTGGC[A/G]TAATCACTAACATTT	54813
rs6572291	snp	A/G	0.300926	0.244758	intron-variant	KLHL28	GRCh38.p7	14:44951903	cctgttgccctggcc[A/G]gggtgtggtggcgag	54813
rs7145870	snp	A/G	0.300926	0.244758	intron-variant	KLHL28	GRCh38.p7	14:44951761	TGCTTAATCAAAACA[A/G]TGTCAACTAGCAACT	54813
rs7147644	snp	A/T	0.127254	0.217792	intron-variant	FAM179B	GRCh38.p7	14:44977157	TTCTGCTTTATATAT[A/T]TGATTGATTGACTAG	54813
rs7147811	snp	A/T	0.301429	0.244653	intron-variant	FAM179B	GRCh38.p7	14:44977228	TGAAGAAAATTAGAC[A/T]GACtttttttttttt	54813
rs7151557	snp	C/T	0.322959	0.239117	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926663	AGGTACCTGCCACAA[C/T]GCCCAGCTAATTTTT	54813
rs7154959	snp	C/T	0.00597247	0.0543191	intron-variant	KLHL28	GRCh38.p7	14:44939452	ctaattttccaagtc[C/T]ttctgttccgcttac	54813
rs7155135	snp	A/C	0.0209421	0.100162	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926996	AGTCTGGGCCAACTA[A/C]AATAGTGCACCTATT	54813
rs7158846	snp	A/G	0.306431	0.243548	intron-variant	KLHL28	GRCh38.p7	14:44954423	AAAAGGCAACTGAcc[A/G]agatttttaaaacaa	54813
rs7492473	snp	A/G	0	0	intron-variant	KLHL28	GRCh38.p7	14:44946020	AATAATCAGATTTGT[A/G]ATTTATTTGTCTGTT	54813
rs8010366	snp	A/G	0.103438	0.202533	intron-variant	KLHL28	GRCh38.p7	14:44946823	ggcttctcaaagtgc[A/G]gggattacaggcatg	54813
rs8017081	snp	G/T	0.312593	0.242037	intron-variant	KLHL28	GRCh38.p7	14:44932257	GAGAGGGGTGGGGGG[G/T]GGGGAGAAAAACCTT	54813
rs8018380	snp	C/T	0.383439	0.21141	intron-variant	KLHL28	GRCh38.p7	14:44941402	TGTGGAAGGCTGAGG[C/T]GGGCAGATCACCTGA	54813
rs9323106	snp	C/T	0.309401	0.24284	intron-variant	FAM179B	GRCh38.p7	14:44977568	TAGAAAAATTCATAG[C/T]TCTTCCTATGAGACC	54813
rs10129173	snp	G/T	0.307671	0.243257	intron-variant	FAM179B	GRCh38.p7	14:44972067	aaccagatctcttga[G/T]aactcactattatga	54813
rs10129201	snp	A/G	0.109108	0.206518	intron-variant	KLHL28	GRCh38.p7	14:44950969	TAAAGAGACATATGA[A/G]CCATTTTAAAATATA	54813
rs10129456	snp	A/G	0.0923359	0.194016	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928404	GGCCCCAAATATCAT[A/G]ATAATAAAAGCAATT	54813
rs10131595	snp	A/T	0.109108	0.206518	intron-variant	KLHL28	GRCh38.p7	14:44955396	agaacacttctagca[A/T]tcagatgtactctct	54813
rs10135494	snp	C/T	0.109814	0.206997	intron-variant	KLHL28	GRCh38.p7	14:44943825	gcctaagcaatcctc[C/T]tgcctcagcctcctg	54813
rs10136688	snp	C/T	0	0	intron-variant	FAM179B	GRCh38.p7	14:44969149	cttccttccttcctt[C/T]ctttcttTCttttct	54813
rs10136741	snp	A/G	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44948303	AATGTACATAAAAAC[A/G]TGATAAACTGTAAGT	54813
rs10136855	snp	A/G	0.310878	0.242475	intron-variant	FAM179B	GRCh38.p7	14:44978556	ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA	54813
rs10136926	snp	A/G	0.314544	0.241524	intron-variant	FAM179B	GRCh38.p7	14:44978578	GGGAGGCCAAGGCAG[A/G]AGGATTGCTTGAGCC	54813
rs10137510	snp	A/G	0.444444	0.157135	intron-variant	KLHL28	GRCh38.p7	14:44941646	aaaaaaaaaaaaaaa[A/G]aaaaagaaaaagaaa	54813
rs10139998	snp	A/G	0.314544	0.241524	intron-variant	FAM179B	GRCh38.p7	14:44979361	ctctgcttcatagac[A/G]gcaccttcttgctgt	54813
rs10140013	snp	C/T	0.300926	0.244758	intron-variant	KLHL28	GRCh38.p7	14:44940078	GGAAGGGTCATCCCA[C/T]GATGGAAGACATCAC	54813
rs10140049	snp	A/G	0.311123	0.242413	intron-variant	FAM179B	GRCh38.p7	14:44979195	aataataataataCT[A/G]TTTTCAAAGGCAGCT	54813
rs10140108	snp	C/T	0.305934	0.243663	intron-variant	KLHL28	GRCh38.p7	14:44940191	ATAACTAACCTACTC[C/T]CACAATAATAGCATT	54813
rs10142624	snp	A/G	0.109461	0.206758	intron-variant	KLHL28	GRCh38.p7	14:44955657	tggatgtggtggcac[A/G]tgcctgtagtctcag	54813
rs10142928	snp	A/G	0.100944	0.200705	intron-variant	KLHL28	GRCh38.p7	14:44955659	gatgtggtggcacat[A/G]cctgtagtctcagct	54813
rs10145267	snp	C/G	0.299916	0.244966	intron-variant	KLHL28	GRCh38.p7	14:44955769	ccagcctgggagaca[C/G]agtgaggccctgcct	54813
rs10147547	snp	A/G	0.109814	0.206997	intron-variant	KLHL28	GRCh38.p7	14:44939181	tagaatgtggagagc[A/G]gactcccaaggtggc	54813
rs10147950	snp	A/C	0.104149	0.203046	intron-variant	KLHL28	GRCh38.p7	14:44939597	ccataaagtcctagg[A/C]aactgatgcaattca	54813
rs10149484	snp	C/T	0.311369	0.242351	intron-variant	FAM179B	GRCh38.p7	14:44971614	tttgctcttcctttg[C/T]tagtttcctaggatg	54813
rs10149748	snp	C/G	0.109814	0.206997	intron-variant	KLHL28	GRCh38.p7	14:44944764	aaaaagaaagaaaga[C/G]agaaaATGGAATAAA	54813
rs10152101	snp	A/C	0.293551	0.246177	intron-variant	KLHL28	GRCh38.p7	14:44951108	AAAAGGGGCTGGCCC[A/C]ATGAAAACTATGGCT	54813
rs11157423	snp	A/T	0.302435	0.244439	utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44960986	TCATTCAAAAGTAAT[A/T]GTATTATTCCTTCAA	54813
rs11157424	snp	A/C	0.302435	0.244439	utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961013	TCAAAAAAAAAAAAT[A/C]TCTCTTCCACACTCC	54813
rs11626430	snp	G/T	0	0	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928828	TTCTCTTTTTTCTTT[G/T]TGATTATTGATTTAC	54813
rs11627736	snp	A/C	0	0	upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962033	CCTTCTCCGCTGTAG[A/C]TGCGTTTACAACGTT	54813
rs11845904	snp	A/G	0.324382	0.238678	intron-variant	KLHL28	GRCh38.p7	14:44935125	tgccatatcatataa[A/G]agaatactacatggc	54813
rs11846502	snp	C/T	0.131381	0.220067	intron-variant	KLHL28	GRCh38.p7	14:44930646	ctttagatttttgaa[C/T]ttggcatgatcaacc	54813
rs11846656	snp	C/T	0.24134	0.24985	intron-variant	FAM179B	GRCh38.p7	14:44977984	AACTGGGCAGCACCA[C/T]GTGAGCTGATTTAAG	54813
rs11846891	snp	C/G	0.137867	0.223442	intron-variant	FAM179B	GRCh38.p7	14:44978504	CTGATAGAAGCAGTA[C/G]TTACTAAAAGAAGAT	54813
rs11847071	snp	A/G	0.118933	0.212888	intron-variant	FAM179B	GRCh38.p7	14:44965855	tttattacactgggg[A/G]cttacaaatagtaat	54813
rs11848799	snp	C/T	0.226779	0.248919	intron-variant	KLHL28	GRCh38.p7	14:44946394	TCATATTAACATACT[C/T]TACCCAAAATTTCAA	54813
rs11850346	snp	G/T	0.0894459	0.191631	intron-variant	FAM179B	GRCh38.p7	14:44974333	tgttacagtgttttt[G/T]atttctaggtttctt	54813
rs11850363	snp	A/G	0.310878	0.242475	intron-variant	FAM179B	GRCh38.p7	14:44974624	TAGTTTTTTAGTAAT[A/G]TACTGTTAAGGTGTG	54813
rs11851962	snp	C/T	0.314301	0.241589	intron-variant	KLHL28	GRCh38.p7	14:44933524	AAAGGTTCAGAATTA[C/T]GATTAATTTCTCATA	54813
rs12147161	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961016	AAAAAAAAAAATATC[C/T]CTTCCACACTCCAAA	54813
rs12184988	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44966010	gtcctgagtagctga[A/G]attacaggctcccac	54813
rs12590192	snp	A/G	0	0	intron-variant	KLHL28	GRCh38.p7	14:44956784	atatattaattaatc[A/G]ctgctattttttgtt	54813
rs12883482	snp	G/T	0	0	intron-variant	KLHL28	GRCh38.p7	14:44942877	ATTATTTTCTACATG[G/T]CTCCTTTACTAAATT	54813
rs17115690	snp	C/T	0.105569	0.204058	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924292	AAAGTTAGCTTGGTT[C/T]AGTTCACAATTATCA	54813
rs17115692	snp	C/T	0.124144	0.21601	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926072	TTTGATCCTTTTTAA[C/T]ATAGAAACATGTGGC	54813
rs17115694	snp	C/G	0.167158	0.235875	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926135	TAATGAAACTTCTCA[C/G]AAATTTGTAAAAGAA	54813
rs17115703	snp	A/C	0.221439	0.248363	intron-variant	KLHL28	GRCh38.p7	14:44947715	AAATCCAACTCTTGA[A/C]ATTTTTATCTTTGTC	54813
rs17115714	snp	A/T	0.109461	0.206758	intron-variant	KLHL28	GRCh38.p7	14:44958055	TCAGGTTCCTCCATA[A/T]CTCTGCCATAGTTTT	54813
rs17115718	snp	C/G	0.306182	0.243605	intron-variant	FAM179B	GRCh38.p7	14:44975180	TTCATTAGCCACTTT[C/G]ACACAGATCAACTGA	54813
rs17115721	snp	C/G	0.0998734	0.199905	intron-variant	FAM179B	GRCh38.p7	14:44976105	AACCCACCTTTCAGA[C/G]TTCTCAAATCTCACC	54813
rs17854942	snp	G/T			synonymous-codon	KLHL28	GRCh38.p7	14:44945914	AAGCATGTAGGTCGG[G/T]GATGTGTGGTCCATC	54813
rs28499068	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44968214	TTTATGTGTGCAGTT[A/T]AAAAAAAGTATATAT	54813
rs28513220	snp	C/T	0.0919752	0.193722	intron-variant	KLHL28	GRCh38.p7	14:44933828	TAGATGTACACACCA[C/T]ACAAAATCTAAAGTT	54813
rs28544334	snp	C/T	0.102726	0.202016	intron-variant	KLHL28	GRCh38.p7	14:44930157	AGAAACAAATTATAG[C/T]AAACACTAAAACAGT	54813
rs28558522	snp	A/C	0.305685	0.24372	intron-variant	KLHL28	GRCh38.p7	14:44950034	TACAGGTAATGGAAC[A/C]GAGGTACTGAGTCTG	54813
rs28690299	snp	A/C	0.103438	0.202533	intron-variant	KLHL28	GRCh38.p7	14:44949676	AAGGATCCTGAAAGA[A/C]TTATATCTAACAAGA	54813
rs28695721	snp	C/T	0.300926	0.244758	intron-variant	KLHL28	GRCh38.p7	14:44942638	CTTCTGAATACCAAT[C/T]AGCTTTTAGTTTCCT	54813
rs28802144	snp	A/G	0.0995161	0.199636	intron-variant	FAM179B	GRCh38.p7	14:44972729	GGTGTACCTTTCTCC[A/G]TCTCTTTACTTTTAA	54813
rs28831119	snp	A/C	0.0995161	0.199636	intron-variant	FAM179B	GRCh38.p7	14:44972631	AGGCCCCTCTTTATC[A/C]CTGATAACTTTTCTT	54813
rs28927673	snp	A/C/G/T	0.0109292	0.0731104	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964053	AAGGATGCTGGTTTT[A/C/G/T]CCTGAGCCCATTGAT	54813
rs34089963	in-del	-/T	0.5	0	intron-variant	FAM179B	GRCh38.p7	14:44975790	CTTTTTTTTTTTTTT[-/T]AATGAAGTGGGTTTG	54813
rs34191093	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44952748	ACTGTGACTATATTT[-/T]GGTTCTCAGCTATCT	54813
rs34218546	in-del	-/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925360	ATATATTTAAAATTT[-/T]CTATAGTTTTCTTAC	54813
rs34356539	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44938256	AAGTTATTTACTTCC[-/C]AAAACACAATGGTGA	54813
rs34373760	snp	A/G	0.00220969	0.0331657	missense	KLHL28	GRCh38.p7	14:44934170	TGTTTTGCTGCAGCG[A/G]TATTGGATGGAATGA	54813
rs34466372	in-del	-/G			intron-variant	KLHL28	GRCh38.p7	14:44948119	AGAATGAATAACAGG[-/G]AAAGGCAAGTAGATA	54813
rs34596250	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44932146	TCTGCCTCAGCCTCC[-/C]TGAGTAGCTAGGACT	54813
rs34684144	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44947945	AGTAGGTACTTTTTT[-/T]CCAGAACATAATATA	54813
rs34924029	in-del	-/G			intron-variant	FAM179B	GRCh38.p7	14:44973648	GACCTATATAATTTT[-/G]CCTTTTCTCTGAAAA	54813
rs35122417	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44957113	CAGGTGTGAGCCCCC[-/C]ATGACCAGCTGTATT	54813
rs35237680	snp	C/T	0.0150606	0.0854603	intron-variant	KLHL28	GRCh38.p7	14:44953360	TATTAGAATAAAATA[C/T]GGGTAAAAACTTATG	54813
rs35264118	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44941718	AAGAGCCACTTTTCC[-/C]ATTTTTATCTTTCTG	54813
rs35338558	in-del	-/C			intron-variant	FAM179B	GRCh38.p7	14:44967894	TTATATGTTATTTCC[-/C]TTGTATTATAAGCAT	54813
rs35352691	snp	A/C	0.00370171	0.042862	missense	KLHL28	GRCh38.p7	14:44934256	GACAATCTTATTTAC[A/C]ATCTGTAGAGAAGTA	54813
rs35428986	in-del	-/AT	0.100231	0.200173	intron-variant	FAM179B	GRCh38.p7	14:44964688	TTAAATTTGAGACAC[-/AT]GTGATATAGACAATA	54813
rs35493028	in-del	-/C			intron-variant	KLHL28	GRCh38.p7	14:44948092	AAAGTTAAAATCTAG[-/C]ACTTAAAAGTAAAGA	54813
rs35612892	in-del	-/G			intron-variant	FAM179B	GRCh38.p7	14:44971589	TTCTCCTGCTCACTT[-/G]TGGATTTAATTTGCT	54813
rs35728857	snp	A/G	0.0075861	0.0611187	missense	KLHL28	GRCh38.p7	14:44934413	CGTCCTGGCGTCACT[A/G]TCAGAAAACATGAAA	54813
rs35780816	in-del	-/A/AA	0	0	intron-variant	FAM179B	GRCh38.p7	14:44964973	AAAAAAAAAAAAAAA[-/A/AA]GGAAAAAGAAAAAGC	54813
rs35910931	in-del	-/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927387	TTAACAATAGTCTAG[-/G]AACATTATGGCACTT	54813
rs56821474	in-del	-/ATAT/ATATAT/ATATATATATATATATATATATATATATAT	0	0	intron-variant	KLHL28	GRCh38.p7	14:44935903	TGTATATATATATAT[lengthTooLong]CTTTACCCTCCCCCC	54813
rs57129780	snp	C/T	0.317933	0.240593	intron-variant	KLHL28	GRCh38.p7	14:44929892	CCTACTCTTCCTTTC[C/T]CTTCACTACAGGAAA	54813
rs57261684	snp	A/C	0.124837	0.216412	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924867	CAATTTTTCTCTCTG[A/C]AGAGATGTAAACTGG	54813
rs57489965	snp	G/T	0.124837	0.216412	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924140	CTCCAAAAGTGCTGG[G/T]GTTACAGGTGTGAGC	54813
rs58271812	in-del	-/CT			intron-variant	FAM179B	GRCh38.p7	14:44973040	CCACTCTGACAATCT[-/CT]GTCTTTTAATTGTTA	54813
rs58836600	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927768	TATTCAGTTACCTAA[A/G]AAATGTACAAAGTAA	54813
rs58920861	snp	C/T	0.208169	0.246476	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924169	GCCACTGAGCCAGGC[C/T]GGGCCTAAGACATGT	54813
rs59360063	snp	C/T	0.0707826	0.174302	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927746	GTTTTCCTCAATAAC[C/T]TTAAAATATTCAGTT	54813
rs60583808	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44967933	GTGATGATTTTTTTT[-/T]AAGGCATTACTCTTA	54813
rs60897331	snp	A/G			upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962080	GGAGACTTTGGCCTA[A/G]TCTCAACACCTGACG	54813
rs61236196	in-del	-/AAAAC	0.0729998	0.176553	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960724	ACCCCCACCCCCCCA[-/AAAAC]AAAACAAAACAAAAC	54813
rs61616302	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44967017	TTTGGTTTTTTTTTT[-/T]CTTGCTTCAGACCTG	54813
rs61998157	snp	A/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44942550	TTTTTTTTTTTTTAA[A/T]TCATGGCATACAATA	54813
rs61998158	snp	A/G	0.187053	0.241946	intron-variant	FAM179B	GRCh38.p7	14:44971105	ATTCTCCCTGCTTCT[A/G]TATTCTGAAGGTAAT	54813
rs61998159	snp	A/G/T			intron-variant	FAM179B	GRCh38.p7	14:44973534	TTAAAAATATGAAAA[A/G/T]TAAGTTTTTTTTTTA	54813
rs62000260	snp	C/T	0.00438332	0.0466095	intron-variant	FAM179B	GRCh38.p7	14:44976265	CTATCTACATTTAAC[C/T]TATTGATTTTCTGGC	54813
rs66488071	snp	C/T	0.235854	0.249599	intron-variant	FAM179B	GRCh38.p7	14:44973618	TACATATATATATAT[C/T]TCTCTCCAGGTTTTT	54813
rs66535982	snp	C/G	0.311123	0.242413	intron-variant	FAM179B	GRCh38.p7	14:44974156	ATACATATGTTACAC[C/G]TTTTGTAGTTTTCCC	54813
rs66662385	snp	C/T	0.225301	0.248777	intron-variant	KLHL28	GRCh38.p7	14:44940118	AAGCGAGTATGTATG[C/T]GAGACAAAGAGAAAA	54813
rs67643245	snp	A/G	0.243633	0.249919	intron-variant	FAM179B	GRCh38.p7	14:44974710	TATGGTTGGCATAAA[A/G]TATCTTAGCATTTTA	54813
rs71412976	snp	C/T	0.5	0	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924259	TCTATGCATAAAACC[C/T]TAAGAGCTGAGCATG	54813
rs71412977	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44965431	ATATCCTACTTGTTT[G/T]TTTCTTTGTTTTTTC	54813
rs71446141	in-del	-/C	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44943958	GTCTCAAGTGATCCT[-/C]CCTGTGTTGGCCTCC	54813
rs72621070	snp	A/G	0.126564	0.217402	intron-variant	FAM179B	GRCh38.p7	14:44974652	GTGGGAGGTGGGGAA[A/G]TGATCTATAGTGCTT	54813
rs72672907	snp	C/T	0.0539704	0.155153	intron-variant	KLHL28	GRCh38.p7	14:44938029	AACACTTTCAAACCA[C/T]AGAATTTTGCCCCTG	54813
rs73334108	snp	G/T	0.00755907	0.0610114	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924949	GTATTAAAAATGTAT[G/T]GTATTCCTCACTCTT	54813
rs73334112	snp	A/T	0.324145	0.238752	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926511	TTTATAATTAAAATC[A/T]TTTTTTTTTTTTGAG	54813
rs73334114	snp	G/T	0.220246	0.248223	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926808	CCACTGCGCCCGTCC[G/T]AAAATCATTTTCCAC	54813
rs73334118	snp	G/T	0.131038	0.219882	intron-variant	KLHL28	GRCh38.p7	14:44930050	AAAAATTCTACTTTA[G/T]ATATTATCTTATATA	54813
rs73334121	snp	C/T	0.131038	0.219882	intron-variant	KLHL28	GRCh38.p7	14:44932560	TAAGATTGTTGGGCT[C/T]GTTCTGGCCCTAACC	54813
rs73334123	snp	C/T	0.00755907	0.0610114	intron-variant	KLHL28	GRCh38.p7	14:44934654	TCAGGGACACAAAAA[C/T]TAAAAGCACAATAAA	54813
rs73334128	snp	A/G	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44935700	GTTCGTAAAAATTCA[A/G]GACAGTGGATACTTC	54813
rs73334131	snp	C/T	0.226779	0.248919	intron-variant	KLHL28	GRCh38.p7	14:44936170	AAACAGGGGGTATAA[C/T]TTTCCAATGATTTTT	54813
rs73334134	snp	C/T	0.00716266	0.059414	intron-variant	KLHL28	GRCh38.p7	14:44936799	TAAAGGAATGATGAC[C/T]GTGATGTTTCTCGAA	54813
rs73334135	snp	A/G	0.300926	0.244758	intron-variant	KLHL28	GRCh38.p7	14:44938784	CAGCCCTGTCCCCAT[A/G]ACTTTGCTGGGCTTA	54813
rs73334137	snp	G/T	0.115788	0.21092	intron-variant	KLHL28	GRCh38.p7	14:44939040	ATGCCCCCATAACTC[G/T]TGTAGTCTGCAAGCC	54813
rs73334142	snp	A/C	0.00716266	0.059414	intron-variant	KLHL28	GRCh38.p7	14:44939806	ATCACCCTTAACATT[A/C]TATTCACGGCAATCT	54813
rs73334148	snp	G/T	0.225005	0.248747	intron-variant	KLHL28	GRCh38.p7	14:44940494	TGCCATCCTTATGAC[G/T]CCTTATGTATAAGTA	54813
rs73334154	snp	C/G	0.305436	0.243776	intron-variant	KLHL28	GRCh38.p7	14:44941054	GCTGTGAGTTGAGAT[C/G]ATGCCAATACATTCC	54813
rs73334157	snp	A/G	0.220544	0.248259	intron-variant	KLHL28	GRCh38.p7	14:44941108	CCTGGGCGACAGAGC[A/G]AGATGCCGTCTCCAA	54813
rs73334162	snp	A/G	0.225005	0.248747	intron-variant	KLHL28	GRCh38.p7	14:44941585	GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC	54813
rs73334165	snp	A/G	0.225301	0.248777	intron-variant	KLHL28	GRCh38.p7	14:44941746	CTGGATCTTTCCAGT[A/G]CATTTTACATAGCTG	54813
rs73334168	snp	A/G	0.00716266	0.059414	intron-variant	KLHL28	GRCh38.p7	14:44941913	TCCTTTTTCCTCTCT[A/G]TATTTTCTCACCAGG	54813
rs73334172	snp	A/C	0.300926	0.244758	intron-variant	KLHL28	GRCh38.p7	14:44942966	CTTTTGTAGAGTTAA[A/C]CTGAATGATCATTCA	54813
rs73334176	snp	C/T	0.225005	0.248747	intron-variant	KLHL28	GRCh38.p7	14:44944558	CATAATTTATATCAG[C/T]ATCCTATTTTTTCTC	54813
rs73334178	snp	C/T	0.115788	0.21092	intron-variant	KLHL28	GRCh38.p7	14:44944728	TGACTCAAATAAACA[C/T]GTAAATGGTTCCAGA	54813
rs73346308	snp	C/T	0.115788	0.21092	intron-variant	KLHL28	GRCh38.p7	14:44947588	AAGTTATGGCAATAA[C/T]GAAAAAGTACATTTG	54813
rs73346313	snp	C/T	0.0883596	0.190715	intron-variant	KLHL28	GRCh38.p7	14:44951650	TAAAAGAAAGCCTAG[C/T]ATATTTTTATAATTG	54813
rs73346324	snp	A/C	0.115788	0.21092	intron-variant	KLHL28	GRCh38.p7	14:44952713	TCAAAAACTATAATG[A/C]CTTCAAAATTATACA	54813
rs73346325	snp	A/C	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44952918	TAAAAAAAAAAAAAA[A/C]AAACACAGGAAAGAA	54813
rs73346327	snp	G/T	0.0437281	0.141251	intron-variant	KLHL28	GRCh38.p7	14:44953916	AAGTAAAAATATAAA[G/T]GAGACTGAGAAAAAT	54813
rs73346329	snp	A/G	0.0640965	0.167152	intron-variant	KLHL28	GRCh38.p7	14:44953967	ATATATCAGTAATAC[A/G]TAAAATATTTCTAAA	54813
rs73346336	snp	A/G	0.214541	0.247473	intron-variant	KLHL28	GRCh38.p7	14:44955719	TGTGCCCAGGAGGTC[A/G]AGGCTGCAGTGTGCA	54813
rs73346337	snp	C/G	0.0107377	0.0726159	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960246	CTCATTTAAGACTTT[C/G]GAAGTTCCTTTTCTG	54813
rs73346344	snp	C/T	0.22263	0.248497	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961152	AAATGTCTACTATCA[C/T]TCCTAAATCCACAAG	54813
rs73346345	snp	A/C/T	0.0947054	0.196675	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961700	AGAGTAACGCGTTTA[A/C/T]AAGGGTGACGAGCCC	54813
rs73346351	snp	A/G	0.23031	0.249223	intron-variant	FAM179B	GRCh38.p7	14:44964651	AGGACCATTTAATAG[A/G]CTTCCTGCTTGATAG	54813
rs73346360	snp	C/G	0.311369	0.242351	intron-variant	FAM179B	GRCh38.p7	14:44966466	CAACAGAGCAAGACT[C/G]CATCTCAAAAATAAT	54813
rs73348277	snp	A/G	0.0103295	0.0711199	intron-variant	FAM179B	GRCh38.p7	14:44967121	AGTATAGATTTGCTC[A/G]TTGCTATTTCTTGCC	54813
rs73348279	snp	G/T	0.109108	0.206518	intron-variant	FAM179B	GRCh38.p7	14:44968740	CATAGTTTACATTAA[G/T]ATTCACTCTTGTGTT	54813
rs73348284	snp	A/G	0.0103295	0.0711199	intron-variant	FAM179B	GRCh38.p7	14:44970171	TCTTCCTATCCACAA[A/G]CATGGATTATCTCTT	54813
rs73348285	snp	A/C	0.136847	0.222927	intron-variant	FAM179B	GRCh38.p7	14:44970321	TGGTAATTTTTTTTA[A/C]ATTTCAAATTCCACT	54813
rs73348288	snp	A/C	0.0558544	0.157504	intron-variant	FAM179B	GRCh38.p7	14:44971722	CGCTTTCACTGCATA[A/C]CGCAAATCTTGATAC	54813
rs73348291	snp	A/G	0.0295035	0.117819	intron-variant	FAM179B	GRCh38.p7	14:44972784	ATGGGTTTCTTGTAG[A/G]CAGCCTATATAGTAA	54813
rs73350114	snp	A/G	0.110872	0.20771	intron-variant	FAM179B	GRCh38.p7	14:44978051	CATGAGATTTTGAGG[A/G]TAATTGGTGATTTGT	54813
rs74046543	snp	C/T	0.0279526	0.114869	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927529	GTTCCAAAATACAAG[C/T]ACCGACATAATAATA	54813
rs74046547	snp	C/T	0.02016	0.0983543	intron-variant	KLHL28	GRCh38.p7	14:44936060	CAGTTTTTATTATAA[C/T]ACTTGTTTTAAAAAT	54813
rs74046548	snp	C/T	0.0205511	0.0992634	intron-variant	KLHL28	GRCh38.p7	14:44939354	AGCACTTGGCTCCCC[C/T]GTAACCACACTCATC	54813
rs74244124	snp	C/T	0.126564	0.217402	intron-variant	KLHL28	GRCh38.p7	14:44938665	GTGAGCCACCGCGCC[C/T]GGCCGAAAACATTAA	54813
rs74244125	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44966632	TTTAACTTTTTCATG[A/G]TAAAATTGTCCCAAA	54813
rs74244127	snp	A/T	0.186421	0.24178	intron-variant	FAM179B	GRCh38.p7	14:44979032	ATAGAAATAACAGAT[A/T]AAAAAAAAAGGTTAG	54813
rs74346360	snp	G/T	0.00914312	0.0669923	intron-variant	FAM179B	GRCh38.p7	14:44965494	GTAGTTTTGTAGAAT[G/T]TCCCAAGTTTTACAT	54813
rs74468035	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948381	AAAACATATCAGTGA[A/G]GAACACAGACTTTGG	54813
rs74543663	snp	A/G	0	0	intron-variant	KLHL28	GRCh38.p7	14:44944747	AATGGTTCCAGAAAG[A/G]AAAAAAGAAAGAAAG	54813
rs74580643	snp	C/G	0.0341408	0.126114	intron-variant	KLHL28	GRCh38.p7	14:44953793	AACAAACTAAGACAA[C/G]CTGAGATTAGGGAAC	54813
rs74601850	snp	C/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44957321	TAAGAGACTTTTTTC[C/T]TAAAAAACAGAAAAT	54813
rs74604643	snp	A/C	0.0554779	0.157039	intron-variant	FAM179B	GRCh38.p7	14:44975284	CATAATATAAAAATA[A/C]ATACTGAGTTGAAGC	54813
rs74719386	snp	A/G			missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964432	CCTGGAATCATGGGA[A/G]AAAACCAGACCTCCA	54813
rs74789218	in-del	-/AA			intron-variant	KLHL28	GRCh38.p7	14:44952916	CATAAAAAAAAAAAA[-/AA]CAAACACAGGAAAGA	54813
rs74908616	snp	C/T	0.115438	0.210697	intron-variant	KLHL28	GRCh38.p7	14:44942076	CATATCCAGCTACCA[C/T]AGAATATCCTTTACC	54813
rs74926176	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44970841	GATGGGTTATATTAA[C/T]TGATTTTCAAATGTT	54813
rs74943361	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44939765	AGAATTTCCCTATGG[-/T]CCTCTTCTTCTGAGC	54813
rs74964079	in-del	-/T	0.300926	0.244758	intron-variant	KLHL28	GRCh38.p7	14:44939766	GAATTTCCCTATGGC[-/T]CTCTTCTTCTGAGCC	54813
rs75014928	snp	A/G	0.0111196	0.0737302	intron-variant	KLHL28	GRCh38.p7	14:44955031	ACACTGTTAATGTGT[A/G]TATTGTGCTATAAAG	54813
rs75015514	snp	A/G	0.0107246	0.0724382	intron-variant	KLHL28	GRCh38.p7	14:44958107	ATGATAAAACAAACA[A/G]TAGTATTCTGAATCT	54813
rs75121536	snp	A/T	0.105214	0.203807	intron-variant	FAM179B	GRCh38.p7	14:44980252	GTCCACATGTAGGAT[A/T]GGTTAGTGACATTAA	54813
rs75237717	snp	A/G	0.109461	0.206758	intron-variant	KLHL28	GRCh38.p7	14:44956158	AAGAGATAGGGTCTT[A/G]CTACCTTGCCGAAAC	54813
rs75421141	snp	C/T	0.0991586	0.199366	intron-variant	FAM179B	GRCh38.p7	14:44965023	TTTGAACTGAGATTT[C/T]CCCCCCAAAGCTTTT	54813
rs75456773	snp	A/G	0.104149	0.203046	intron-variant	KLHL28	GRCh38.p7	14:44938855	TTCTGACAGGCTGAC[A/G]TTGCACACTACTTGC	54813
rs75462719	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44970836	GATGTGATGGGTTAT[A/G]TTAATTGATTTTCAA	54813
rs75642191	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44950791	CAGTAATTGGTAGAC[A/G]TTATTTATTTTTACT	54813
rs75664376	snp	A/G	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44929659	ATGGGGGGCCTACTG[A/G]AGCAATATGAGCTTG	54813
rs75721453	snp	A/T	0.0252325	0.109451	intron-variant	FAM179B	GRCh38.p7	14:44970313	AATGTAAATGGTAAT[A/T]TTTTTTAAATTTCAA	54813
rs75807858	snp	A/C/G	0.103189	0.202727	intron-variant	KLHL28	GRCh38.p7	14:44956196	AATCTCCTGGTCTTA[A/C/G]GCGATCCTCCCACCT	54813
rs75830358	snp	C/T	0.00358779	0.0422022	intron-variant	FAM179B	GRCh38.p7	14:44976069	CAGAATTGGTCTTTC[C/T]AAGAATGAATCTGAT	54813
rs76006069	snp	C/G	0.214541	0.247473	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926896	TATATTTAATAATTT[C/G]ATTGCTATAAACAAA	54813
rs76024027	snp	C/T	0.00914312	0.0669923	intron-variant	KLHL28	GRCh38.p7	14:44937825	AGCCTGTGCACAAGA[C/T]AGAGAAAATGGCAGC	54813
rs76364389	snp	G/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44937162	TCTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCA	54813
rs76447192	snp	A/C	0.107341	0.205301	intron-variant	KLHL28	GRCh38.p7	14:44959670	GTAGCACACACATTC[A/C]TATAATTCACTAATT	54813
rs76726428	snp	C/G	0.221439	0.248363	intron-variant	KLHL28	GRCh38.p7	14:44941423	GATCACCTGAGGTCA[C/G]GAGTTCGAGACCAGC	54813
rs76770586	snp	A/C/G	0.0998734	0.199905	intron-variant	FAM179B	GRCh38.p7	14:44975256	ATGCCCCCCCACCAG[A/C/G]TGAAAGCCTAAACAT	54813
rs76798803	snp	C/T	0.0252325	0.109451	intron-variant	FAM179B	GRCh38.p7	14:44969742	GGGTGTCAGGTCTGT[C/T]TCTAGATTCATTTTT	54813
rs76915423	snp	G/T	0.5	0	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926523	ATCTTTTTTTTTTTT[G/T]GAGGTGGAGTTTCAC	54813
rs77047006	snp	G/T	0.0995161	0.199636	intron-variant	KLHL28	GRCh38.p7	14:44955310	GTAATATTATTTTAA[G/T]GAAAAAAATAAATTA	54813
rs77135108	snp	C/G	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44936800	AAAGGAATGATGACT[C/G]TGATGTTTCTCGAAT	54813
rs77221389	snp	C/T	0.109814	0.206997	intron-variant	KLHL28	GRCh38.p7	14:44943079	TATTATGATAGATTC[C/T]ATGATAAAAGATTAC	54813
rs77240482	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44964586	TTTGTTTTAAATTGA[C/T]TTTAAATCCATCTGA	54813
rs77247321	snp	G/T	0.5	0	intron-variant	FAM179B	GRCh38.p7	14:44970911	GTGGTGTGTTATTCA[G/T]TTTGTATATTGTTGG	54813
rs77311023	snp	G/T	0.5	0	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924678	ACACAGCACAATTCA[G/T]AAGGCAAAAATATAG	54813
rs77338453	in-del	-/TT	0	0	intron-variant	FAM179B	GRCh38.p7	14:44976648	TTTAAAAAAAAACTC[-/TT]AAAATAATACCTGAA	54813
rs77347835	snp	A/G	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44973065	TTGTTAGACATTTAA[A/G]GAGTTTATTGATATA	54813
rs77492628	snp	C/T	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44974371	CCTTCTTAGAAGTAA[C/T]GCTTCATGACTTATA	54813
rs77495267	snp	G/T	0.5	0	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926524	TCTTTTTTTTTTTTT[G/T]AGGTGGAGTTTCACT	54813
rs77679984	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44947470	ATTAATACATGGATA[A/T]TTCAGAATGGATTGT	54813
rs77718288	in-del	-/T	0.222035	0.248431	intron-variant	KLHL28	GRCh38.p7	14:44957313	TGCACAGTAAGAGAC[-/T]TTTTTTCTTAAAAAA	54813
rs77832563	snp	A/T	0.5	0	intron-variant	FAM179B	GRCh38.p7	14:44980290	ATTTCCAGAAAAAAA[A/T]TCATGAATATTTCAA	54813
rs77944803	snp	A/G/T	0.00993945	0.0698483	intron-variant	FAM179B	GRCh38.p7	14:44972371	TAAAGTAATCTATAG[A/G/T]TGTCAATTACATCTA	54813
rs77953810	snp	A/G	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44939049	TAACTCTTGTAGTCT[A/G]CAAGCCTGTAGAGTT	54813
rs77998493	snp	A/C	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44941633	AACTCTGTCTCAAAA[A/C]AAAAAAAAAAAAGAA	54813
rs78165946	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962083	GACTTTGGCCTAGTC[C/T]CAACACCTGACGTGG	54813
rs78184313	snp	C/T	0.0174175	0.0916809	intron-variant	KLHL28	GRCh38.p7	14:44944165	CATGAAGCAATCCTA[C/T]CTAAGAAAAAGCAAA	54813
rs78203513	snp	A/G	0.00398564	0.0444627	intron-variant	FAM179B	GRCh38.p7	14:44967874	TTTCAGATTTATATA[A/G]TCTGGTTATATGTTA	54813
rs78323216	snp	A/C	0.104504	0.2033	intron-variant	KLHL28	GRCh38.p7	14:44936243	GGGGCAGAGAAAGAC[A/C]ATGGGACCAGAGGGG	54813
rs78360266	snp	C/G	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44958750	AGTTACATAATTAAT[C/G]CCTGTCCACTGAAAA	54813
rs78701909	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44974610	GGAACTGTGGTAAAT[A/T]GTTTTTTAGTAATAT	54813
rs78899501	snp	G/T	0.111928	0.208413	downstream-variant-500B	KLHL28	GRCh38.p7	14:44923919	CTGTTGTCCAGGCTG[G/T]AATGCAATGGCGCCA	54813
rs78967067	in-del	-/A	0.214843	0.247516	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927478	ATCGCAAACAGGTTT[-/A]AAAAAAATCAAGGAA	54813
rs79030011	snp	C/T	0.0111196	0.0737302	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925775	CATTTAAAACAATAA[C/T]AGCAATAACACAATT	54813
rs79049744	snp	C/T	0.0414363	0.137845	intron-variant	KLHL28	GRCh38.p7	14:44932694	ATTAGACCAAAATCA[C/T]TGAAGAAGAGTTGAT	54813
rs79158941	snp	A/C	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44942744	TTGCTTAGCATTCAA[A/C]ACTCAACTTGTACAT	54813
rs79212272	snp	A/G	0.00358779	0.0422022	intron-variant	KLHL28	GRCh38.p7	14:44953193	AGGTGGAATCTCTGC[A/G]AGGGAAAAGAGAAAC	54813
rs79258150	snp	C/G	9.94415e-05	0.00705059	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962622	TACAACTTCGCCTCT[C/G]GCCTCGGCCCTCTTG	54813
rs79367070	snp	A/G	0.00597247	0.0543191	intron-variant	KLHL28	GRCh38.p7	14:44948854	TAACTTTACCTGGAC[A/G]TCTATAAGCATTTAT	54813
rs79397696	snp	A/T	0	0	intron-variant	FAM179B	GRCh38.p7	14:44965870	GCTTACAAATAGTAA[A/T]TTTTTTTTTTTTTTT	54813
rs79409108	snp	C/T	0.0154538	0.0865337	intron-variant	KLHL28	GRCh38.p7	14:44941727	CTTTTCCATTTTTAT[C/T]TTTCTGGATCTTTCC	54813
rs79628027	snp	C/T	0.0170251	0.090679	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927706	CTCAACTTAGAACTA[C/T]TACTCAAGTAAACAT	54813
rs79691475	in-del	-/CT			intron-variant	FAM179B	GRCh38.p7	14:44973039	ACCACTCTGACAATC[-/CT]TSTCTTTTAATTGTT	54813
rs79802666	snp	C/G	0.0236746	0.106192	intron-variant	FAM179B	GRCh38.p7	14:44975184	TTAGCCACTTTGACA[C/G]AGATCAACTGAAAAC	54813
rs79848527	snp	G/T	0.0111196	0.0737302	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927064	ATTGCTATATATTAT[G/T]ATGTTATTCAGACAA	54813
rs79851852	snp	A/C	0.0142736	0.0832652	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928152	GATCTTAAAAAACTA[A/C]AATTATAAGGATATA	54813
rs79923799	snp	G/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44933327	TCTTTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA	54813
rs79983664	snp	C/T	0.0123036	0.0774623	intron-variant	FAM179B	GRCh38.p7	14:44979067	AGATGAATTTTGATA[C/T]AACAATTAGGAGTCA	54813
rs80059988	snp	C/T	0.0053601	0.051491	missense, intron-variant	KLHL28	GRCh38.p7	14:44931533	TTACTTGGATCATAA[C/T]GCTCCACACTGCAAA	54813
rs80132788	snp	A/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44958403	ACTCTTAAAAAAAAA[A/T]TTCAAACCGACAGTT	54813
rs80139033	snp	C/T	0.100588	0.200439	intron-variant	KLHL28	GRCh38.p7	14:44948423	AATGAGTTTTAGTCC[C/T]ATCTGAATCTTAAAT	54813
rs80272555	snp	G/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44938389	CTTCTTTTTTTTTTT[G/T]GAGACTGAGTCTCGC	54813
rs111053517	snp	A/C	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44966555	TTCTCTGTTTACTAC[A/C]TGCAATTCTTTTTTT	54813
rs111403608	snp	C/G	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44936763	CGGAGGAACAGAAAG[C/G]CAAAGGGGCCATGGC	54813
rs111403989	snp	C/G	0.0111196	0.0737302	intron-variant	FAM179B	GRCh38.p7	14:44964831	GGCCAGTTTCACACA[C/G]TATAGGAAAAAGGTC	54813
rs111422993	snp	C/T	0.5	0	synonymous-codon	KLHL28	GRCh38.p7	14:44945455	ATTCTGGCATATGTA[C/T]TTAGTGGCTGCCAAA	54813
rs111464709	snp	C/T	0.5	0	intron-variant	FAM179B	GRCh38.p7	14:44976042	TGATTCCTAGATCAA[C/T]TATACTGATTTCAGA	54813
rs111523671	snp	A/G	0.5	0	intron-variant	FAM179B	GRCh38.p7	14:44971685	ATATATGCCTTCAGT[A/G]CCATAAATTTCCTCT	54813
rs111541733	snp	G/T	0.00914312	0.0669923	intron-variant	FAM179B	GRCh38.p7	14:44965825	AGCATCCACCAATGG[G/T]CTTTACCTGTATCAT	54813
rs111544520	snp	C/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44938854	GTTCTGACAGGCTGA[C/T]GTTGCACACTACTTG	54813
rs111574159	snp	C/T	0.00914312	0.0669923	intron-variant	FAM179B	GRCh38.p7	14:44969303	ACTACAGGCCCACAC[C/T]ATCATGCCCGGCTAA	54813
rs111659810	snp	A/C	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44931882	GTGGATTTGTGTAAT[A/C]CTGAATAAGTCATTT	54813
rs111753871	snp	C/T	0.00597247	0.0543191	intron-variant	KLHL28	GRCh38.p7	14:44930378	CTAGCGATTCTCATG[C/T]CTCAGCCTCCCGAGT	54813
rs111842421	snp	C/T	0.00597247	0.0543191	intron-variant	KLHL28	GRCh38.p7	14:44952069	TTTCACCATGTTGCC[C/T]AGGCTAGTCTCGAAC	54813
rs111887188	in-del	-/TC	0.311123	0.242413	intron-variant	FAM179B	GRCh38.p7	14:44973037	TGACCACTCTGACAA[-/TC]TCTGTCTTTTAATTG	54813
rs111985018	snp	A/G	0	0	intron-variant	FAM179B	GRCh38.p7	14:44973126	TTCTATTTGTTGCTC[A/G]TGATCTTTGTTCCTG	54813
rs112033044	snp	A/C	0.00914312	0.0669923	intron-variant	KLHL28	GRCh38.p7	14:44952690	AGGTGTCCACCACTG[A/C]GTTTGGCTCAAAAAC	54813
rs112121879	snp	C/T	0	0	intron-variant	FAM179B	GRCh38.p7	14:44976649	TTAAAAAAAAACTCT[C/T]AAAATAATACCTGAA	54813
rs112186695	in-del	-/C	0.219049	0.248077	intron-variant	KLHL28	GRCh38.p7	14:44937058	CATCTGAAGTAGGAA[-/C]AGTCTAGGACTGAGC	54813
rs112270973	in-del	-/A	0.5	0	intron-variant	FAM179B	GRCh38.p7	14:44978818	AATTAAAAAAAAGAG[-/A]AAAAAAAAAGAAGAA	54813
rs112323342	in-del	-/GGC	0.222333	0.248464	intron-variant	KLHL28	GRCh38.p7	14:44941440	GTTCGAGACCAGCCT[-/GGC]CAGCATGGAGAAACC	54813
rs112362273	snp	A/T	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44934619	CCCATAAAGACAGAT[A/T]TGTTTAATCTTATTA	54813
rs112386910	snp	A/C	0.00914312	0.0669923	intron-variant	KLHL28	GRCh38.p7	14:44952914	ACCATAAAAAAAAAA[A/C]AAACAAACACAGGAA	54813
rs112435177	snp	C/T	0.0558544	0.157504	intron-variant	KLHL28	GRCh38.p7	14:44938607	AATCTCCTGACCTCG[C/T]GATCTGCCCGCCTTG	54813
rs112454594	in-del	-/TT	0	0	intron-variant	KLHL28	GRCh38.p7	14:44943717	AATGTATTATCGGAC[-/TT]TTTTTTTTTTTTTTC	54813
rs112507516	in-del	-/T/TTTCT	0	0	intron-variant	FAM179B	GRCh38.p7	14:44969150	TCCTTCCTTCCTTTC[-/T/TTTCT]TTTCTTTCTTTTCTT	54813
rs112555230	snp	C/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44938066	AAAATTCGTGTCCTT[C/T]TCACATGCAAAATAT	54813
rs112593192	snp	A/C	0.0252325	0.109451	intron-variant	KLHL28	GRCh38.p7	14:44932351	AGTACAAACTGGCTG[A/C]TCATAATTATCTCAG	54813
rs112595029	in-del	-/A	0	0	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926510	TTTATAATTAAAATC[-/A]TTTTTTTTTTTTTGA	54813
rs112606992	snp	A/G	0.00914312	0.0669923	intron-variant	FAM179B	GRCh38.p7	14:44971669	TCTTTCTTCTTTTCT[A/G]ATATATGCCTTCAGT	54813
rs112641941	snp	A/T	0.104149	0.203046	intron-variant	KLHL28	GRCh38.p7	14:44938621	GCGATCTGCCCGCCT[A/T]GGCCTCCCAAAGTGC	54813
rs112642141	snp	A/G	0.00914312	0.0669923	intron-variant	KLHL28	GRCh38.p7	14:44952963	ATTAATTTTAGAGTC[A/G]GACAGATTTGGATTT	54813
rs112696182	snp	A/G	0	0	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927200	ATATTCATAAAGCAT[A/G]ATACTACATTTATGA	54813
rs112698865	snp	G/T	0	0	intron-variant	FAM179B	GRCh38.p7	14:44968711	ATATTAACATATAAT[G/T]ATCACCCAAGGCCCA	54813
rs112703519	snp	G/T	0.5	0	intron-variant	FAM179B	GRCh38.p7	14:44977814	CCATGCCCAGCTAAT[G/T]TTTTTTGTATTTTTT	54813
rs112859592	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925365	ATTTAAAATTTCTAT[A/G]GTTTTCTTACTAGAA	54813
rs112897777	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967368	TAACCCCCCTCCCCC[C/G]ACAAAATTGCTAGAC	54813
rs112905747	snp	A/G/T	0	0	intron-variant	KLHL28	GRCh38.p7	14:44954510	GCAGTACTATACAGC[A/G/T]ATGAAAAGGAATGAG	54813
rs112910852	snp	A/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44955788	GAGGCCCTGCCTCAA[A/T]ATAAATAAATAAATA	54813
rs112959037	snp	A/G	3.29728e-05	0.00406021	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962970	AGCACTTTTGCCTCA[A/G]CTAGTTGTCTCGTTA	54813
rs112976857	in-del	-/TT	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44940154	GCAGGACTTATCTTA[-/TT]ATCAGGAGCCCACTC	54813
rs113165260	snp	A/T	0.0498117	0.149749	intron-variant	FAM179B	GRCh38.p7	14:44977595	GACCCCACACAGAGA[A/T]ATTTTAAATATGTTG	54813
rs113215069	snp	C/T	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44929203	ACTCCTAGGAAAGGT[C/T]GGCAAAAAGAAGATA	54813
rs113242921	snp	A/G	0.221439	0.248363	intron-variant	KLHL28	GRCh38.p7	14:44941419	GGCAGATCACCTGAG[A/G]TCAGGAGTTCGAGAC	54813
rs113302242	in-del	-/T	0	0	downstream-variant-500B	KLHL28	GRCh38.p7	14:44923877	CTATGACATATTTTC[-/T]TTTTTTTTTTGAGAT	54813
rs113318341	in-del	-/GT	0	0	intron-variant	KLHL28	GRCh38.p7	14:44932253	GAAGAGAGGGGTGGG[-/GT]GGGTGGGGAGAAAAA	54813
rs113394270	snp	A/G	0.0111196	0.0737302	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927287	TATGGAAGAACAAAG[A/G]ACTGTAAATTGCCCG	54813
rs113412368	snp	A/C	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44930384	ATTCTCATGCCTCAG[A/C]CTCCCGAGTAGCTGA	54813
rs113438036	snp	A/G	0.5	0	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927561	AATGCAAGTGAATGT[A/G]TTTAAGACTAACAGA	54813
rs113485366	snp	A/G	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44946808	TGATCCACCTGCTTC[A/G]GCTTCTCAAAGTGCG	54813
rs113590577	snp	C/G	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44937820	TAGCAAGCCTGTGCA[C/G]AAGACAGAGAAAATG	54813
rs113613348	snp	A/G	0.221439	0.248363	intron-variant	KLHL28	GRCh38.p7	14:44941430	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTCAGCA	54813
rs113785100	snp	A/G	0.5	0	intron-variant	KLHL28	GRCh38.p7	14:44931870	AACCCTACTGCTGTG[A/G]ATTTGTGTAATCCTG	54813
rs113875500	snp	C/T	0.5	0	missense	KLHL28	GRCh38.p7	14:44945582	AGGACAAGTTTTATC[C/T]GGAGTAGGTTTGCTG	54813
rs113909436	snp	C/T	0.0640965	0.167152	intron-variant	FAM179B	GRCh38.p7	14:44965935	GCTGGAGCGCAATGG[C/T]GCAATCTCAGCTCAC	54813
rs113962308	snp	A/G	0.00914312	0.0669923	intron-variant	KLHL28	GRCh38.p7	14:44931935	ATAGTGCAACCTGAA[A/G]GGATTCATATAAGAA	54813
rs113966848	snp	A/G	0	0	intron-variant	FAM179B	GRCh38.p7	14:44971613	ATTTGCTCTTCCTTT[A/G]TTAGTTTCCTAGGAT	54813
rs114085255	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962210	GTGCCCTTGGTTACG[C/T]CCGGTGGCAGCTGTG	54813
rs114246781	snp	G/T	0.0189856	0.0955633	intron-variant	FAM179B	GRCh38.p7	14:44967077	TACTGCCTTTTTATT[G/T]GGCAGTGGTATTTGA	54813
rs114263757	snp	A/G	0.0115144	0.0749975	intron-variant	FAM179B	GRCh38.p7	14:44977110	AAGTAAAATTAATCA[A/G]TGTAGCTATCAAATG	54813
rs114318796	snp	A/T	0.031825	0.122064	intron-variant	FAM179B	GRCh38.p7	14:44965036	TTTCCCCCCAAAGCT[A/T]TTATTTAAAAAATTC	54813
rs114387160	snp	C/T	0.0123036	0.0774623	intron-variant	FAM179B	GRCh38.p7	14:44972658	TCTTGCTCTGAAGTC[C/T]GCTGTGTCTGAAATT	54813
rs114514550	snp	G/T	0.0166325	0.0896639	intron-variant	KLHL28	GRCh38.p7	14:44958897	GAAGATAAACCTAAG[G/T]AGATGAAAATATATC	54813
rs114630737	snp	C/T	0.030278	0.119257	intron-variant	KLHL28	GRCh38.p7	14:44943966	GTGATCCTCCTGTGT[C/T]GGCCTCCCAAAGTGC	54813
rs114687551	snp	C/G	0.0178098	0.0926698	intron-variant	KLHL28	GRCh38.p7	14:44939072	GTAGAGTTAACATCA[C/G]ATGGCCAACACCAAA	54813
rs114881159	snp	A/G	0.00953873	0.0683987	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961637	CAGATCTTCTGTCCT[A/G]ATAAGCAGATGGCAA	54813
rs114885319	snp	A/G	0.0174175	0.0916809	intron-variant	KLHL28	GRCh38.p7	14:44951328	TCCAGGAGAATCACA[A/G]GGTGTGTCAAGCCAC	54813
rs115019397	snp	A/G	0.00755907	0.0610114	intron-variant	KLHL28	GRCh38.p7	14:44937842	GAGAAAATGGCAGCC[A/G]GACTTATCCTTTTAT	54813
rs115193922	snp	A/G	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44955128	GAAAAAGAAGGTAAC[A/G]ACATAACACTAAGAT	54813
rs115217634	snp	A/C/T	0.101385	0.201329	intron-variant	FAM179B	GRCh38.p7	14:44965988	CAAACGATTCTCCCA[A/C/T]CTCAGTGTCCTGAGT	54813
rs115545244	snp	C/G	0.0138799	0.0821421	intron-variant	KLHL28	GRCh38.p7	14:44951557	TGAACCAGCATGGTT[C/G]ATTTTACTCCATAAT	54813
rs115555158	snp	C/T	0.030278	0.119257	intron-variant	KLHL28	GRCh38.p7	14:44959684	CCTATAATTCACTAA[C/T]TTAACTACATTCTTG	54813
rs115671681	snp	C/T	0.0103295	0.0711199	utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44960985	GTCATTCAAAAGTAA[C/T]AGTATTATTCCTTCA	54813
rs115843672	snp	C/T	0.030278	0.119257	intron-variant	KLHL28	GRCh38.p7	14:44949165	AGGACTGAAGACTAT[C/T]TTCAAAAATAAGACA	54813
rs116023250	snp	A/G	0.0185938	0.0946107	intron-variant	KLHL28	GRCh38.p7	14:44933752	GACACACAGGAATTA[A/G]ATTTCTACTTCTTTA	54813
rs116079344	snp	A/G	0.00438332	0.0466095	intron-variant	FAM179B	GRCh38.p7	14:44968815	CAGTACATTCTGTGG[A/G]GTTTTGACAAATGTA	54813
rs116188814	snp	C/T	0.00993419	0.0697739	intron-variant	KLHL28	GRCh38.p7	14:44944231	TACTAGTATAATGCA[C/T]CAAATTAAGGGTTGG	54813
rs116528850	snp	G/T	0.0154538	0.0865337	intron-variant	KLHL28	GRCh38.p7	14:44956149	TTGTTTTTTAAGAGA[G/T]AGGGTCTTGCTACCT	54813
rs116559027	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44980232	TAATCTGTTATTTCT[A/G]TCTTGTCCACATGTA	54813
rs116613076	snp	C/T	0.104149	0.203046	intron-variant	FAM179B	GRCh38.p7	14:44970982	TGTTCATAGGTGATA[C/T]TGGTCTGTGGGGTTT	54813
rs116898698	snp	A/C	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44959854	ATTTGTACTCTCTCT[A/C]TATATGATTAAATAC	54813
rs116920413	snp	A/G	0.00478085	0.0486577	intron-variant	KLHL28	GRCh38.p7	14:44946041	TTTGTCTGTTCATTG[A/G]TTTTTAAATACTTCA	54813
rs117076886	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962045	TAGCTGCGTTTACAA[C/T]GTTCTGACTTCCTCT	54813
rs117098369	snp	A/G	0.030665	0.119967	intron-variant	FAM179B	GRCh38.p7	14:44980174	GCCTGATTTGTACTG[A/G]CTCTTGGCCAGGCTC	54813
rs117295933	snp	A/C	0.0240756	0.107043	missense	KLHL28	GRCh38.p7	14:44934496	ATTCCAAATTCATAG[A/C]GAGGAATGTTTAGGG	54813
rs117341422	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44940406	TTATAGTGTTGAGAT[A/G]AGTGATGTGGCTGAA	54813
rs117428938	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44936749	CTAGATGAGTATGAC[A/G]GAGGAACAGAAAGGC	54813
rs117477200	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44963995	TAGATAGCAAACGCA[A/G]GGTACGCCAAGCAGC	54813
rs117727385	snp	A/G	0.0126979	0.078662	intron-variant	FAM179B	GRCh38.p7	14:44980133	ATTCATGTGTCCTCC[A/G]TACTCAGTTACAGGT	54813
rs117874812	snp	C/G	0.0142736	0.0832652	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924240	ACTCTATGGCTACTA[C/G]CTATCTATGCATAAA	54813
rs118041531	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44962118	CATAACCCAGCATTC[A/G]TCACGGCAAGTGGAT	54813
rs118117258	snp	A/C	0.0248432	0.108648	intron-variant	KLHL28	GRCh38.p7	14:44951154	CTGTAGCTCTATTCT[A/C]AGGGTGTGGGATGGG	54813
rs118149517	snp	A/C/G	0.0189856	0.0955633	intron-variant	KLHL28	GRCh38.p7	14:44958250	TAAAGGTCAAGTTGC[A/C/G]AGTTTTGTACCTATC	54813
rs137971160	snp	C/T	0.0111196	0.0737302	intron-variant	KLHL28	GRCh38.p7	14:44939813	TTAACATTCTATTCA[C/T]GGCAATCTAGGCTTC	54813
rs138043791	snp	C/T	0.100231	0.200173	intron-variant	FAM179B	GRCh38.p7	14:44975554	TCACTGCAACCTCTG[C/T]CTCCCAGGTTCAAGC	54813
rs138105043	snp	A/T	0.000153988	0.00877328	synonymous-codon	KLHL28	GRCh38.p7	14:44945587	AAGTTTTATCTGGAG[A/T]AGGTTTGCTGCTGGC	54813
rs138190737	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970005	TGTTTTCCTTCCATG[A/T]TGAGTTCACTCTTCT	54813
rs138249766	snp	A/T	0.00636936	0.0560724	intron-variant	FAM179B	GRCh38.p7	14:44965043	CCAAAGCTTTTATTT[A/T]AAAAATTCCAAATCT	54813
rs138298952	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954758	AATATACTCTGTTTT[A/G]TAGATTTGACTGTGG	54813
rs138310983	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960250	TTTAAGACTTTCGAA[A/G]TTCCTTTTCTGTGAT	54813
rs138319527	snp	A/G	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44946718	CTGCTAACATGCCTG[A/G]CTAATTTTTATATTT	54813
rs138391813	snp	A/G	0.00636936	0.0560724	intron-variant	KLHL28	GRCh38.p7	14:44958627	TTATTGACAAACAAA[A/G]GAAAAGTAAAATTAG	54813
rs138559035	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970703	CTATAAAGTTGAGAA[A/G]GTTCCCCCTGTATTC	54813
rs138576852	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44929945	GGCTATTTTTTTTTA[A/G]TTTCATTTCATTCTA	54813
rs138627625	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940405	TTTATAGTGTTGAGA[A/T]GAGTGATGTGGCTGA	54813
rs138649560	snp	C/T	0.0260105	0.111035	intron-variant	KLHL28	GRCh38.p7	14:44935988	AAAAAAGTCCTCCAT[C/T]CAGTATAATCAAGCT	54813
rs138687321	in-del	-/T	0.259674	0.249813	intron-variant	FAM179B	GRCh38.p7	14:44973538	ATAAGTTTTTTTTTT[-/T]AACCTTTACTTATTC	54813
rs138856192	snp	A/C	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44959852	AAATTTGTACTCTCT[A/C]TATATATGATTAAAT	54813
rs138861593	snp	C/T	4.94425e-05	0.0049718	synonymous-codon	KLHL28	GRCh38.p7	14:44945755	CATAGCTTTGAAATA[C/T]GGGCTGACGCTGGCA	54813
rs138890253	snp	A/C/T	0.000164985	0.00908114	missense, intron-variant	KLHL28	GRCh38.p7	14:44931465	CTAGCATGACACCCA[A/C/T]GCCAAAGTGAATCCT	54813
rs138985688	snp	C/T	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44931041	ATGACATTTGTTACA[C/T]GGACAAAAGGAGCTT	54813
rs139050349	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44967507	AATTAAGTCTTTTAT[C/T]TATGTAATTATTATT	54813
rs139118130	snp	G/T	0.000247135	0.0111134	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964106	AACTGCAAGATAATG[G/T]AGATGGAGTGATGAA	54813
rs139248596	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971721	CCGCTTTCACTGCAT[A/C]CCGCAAATCTTGATA	54813
rs139330757	snp	G/T	0.0111196	0.0737302	intron-variant	KLHL28	GRCh38.p7	14:44936894	TGATTATGGGGCCAA[G/T]GGATGAAGAATCCTG	54813
rs139341319	snp	A/G	3.2962e-05	0.00405954	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963859	CTCCTGGAACATCTC[A/G]AACATAAGCATTCCA	54813
rs139355471	snp	A/T	0.0023933	0.0345097	intron-variant	FAM179B	GRCh38.p7	14:44972461	CTGTCCATTTCTGAT[A/T]GAGGGGTAATTAAGT	54813
rs139363568	in-del	-/ATGTATGTATGTGTAT			intron-variant	KLHL28	GRCh38.p7	14:44935852	TATATAATCTTTTGC[-/ATGTATGTATGTGTAT]GTGTATGTATATATA	54813
rs139388902	snp	A/G	0.000510847	0.0159738	synonymous-codon	KLHL28	GRCh38.p7	14:44934213	CGTCATTGGTGCCAC[A/G]GGTTGCCATTTTCTT	54813
rs139529784	snp	G/T	0.0107246	0.0724382	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961355	TGCATTAGAAGGAAA[G/T]ATTTTGATAACGTCT	54813
rs139626049	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961182	GGCAGAATTCTCTTA[G/T]AACCATGATGCCAAG	54813
rs139648915	snp	C/G	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44947909	GGTATAAACAAGTCC[C/G]AAGAAGCTTCTGGGT	54813
rs139690301	snp	G/T	0.0130921	0.0798413	intron-variant	KLHL28	GRCh38.p7	14:44956256	ATGAGCCACTACACC[G/T]GGCCAAATTTCTCTT	54813
rs139700181	snp	A/G	0.00318978	0.0398085	intron-variant	KLHL28	GRCh38.p7	14:44949818	GGGATTTTAATTGCA[A/G]TACTATTTTAACACC	54813
rs139707349	in-del	-/TATA/TATATA/TATATATATATATATATATATATATA	0.42357	0.179927	intron-variant	KLHL28	GRCh38.p7	14:44935890	ATATATATATGTGTG[lengthTooLong]TATATATATATATCT	54813
rs139748762	in-del	-/A	0.0626037	0.165477	intron-variant	KLHL28	GRCh38.p7	14:44958394	ATCAAGATTACTCTT[-/A]AAAAAAAAATTCAAA	54813
rs139947112	snp	G/T	1.80546e-05	0.00300449	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964456	ACCTCCACTTCCAAG[G/T]ATATAGAGCAGGTAT	54813
rs140024048	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968528	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	54813
rs140044612	snp	A/G	0.00597247	0.0543191	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937564	ATGGATTATCTGTAA[A/G]TTATGGATTTCTGGA	54813
rs140096970	snp	C/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44932726	CACTGCAGCAAGACT[C/T]TCAAGATAATCAAAT	54813
rs140246403	snp	A/G	0.000276491	0.0117545	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962495	ATCGGCTCCAGAGCC[A/G]CAGTCGTCCTTCCGC	54813
rs140285321	snp	C/T	0.00398564	0.0444627	intron-variant	KLHL28	GRCh38.p7	14:44939591	TGCATTCCATAAAGT[C/T]CTAGGAAACTGATGC	54813
rs140361174	snp	C/T	0.000137075	0.00827762	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962785	CAAGCTGCTTTGCCG[C/T]GGCGGGGCGGTCGAC	54813
rs140441001	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44978782	ACTAGCCTGGGAGAC[A/G]AAGTGAGACCTTGTC	54813
rs140536679	snp	G/T	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44939140	CACATCTGGGCCTAT[G/T]TGAGCCACAGCTGGG	54813
rs140640165	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955835	AAAGCTATCAAATAC[C/T]ACAAGAGTCATATAA	54813
rs140714035	snp	C/T	0.00795532	0.062565	intron-variant	KLHL28	GRCh38.p7	14:44952475	AAAATATTTATAGCT[C/T]AAGTTTAGCAGCTTA	54813
rs140734662	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958061	TCCTCCATATCTCTG[C/T]CATAGTTTTTGTTCT	54813
rs140841276	snp	C/G	0.00438332	0.0466095	intron-variant	KLHL28	GRCh38.p7	14:44943276	TGCATTTCAGAATAA[C/G]AGTTAAACAATCAAT	54813
rs140877869	snp	C/T	0.0115144	0.0749975	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926232	TAGGTTAAGCAATCC[C/T]AAAATAAATATACTT	54813
rs140925253	in-del	-/AC	0.311614	0.242289	intron-variant	FAM179B	GRCh38.p7	14:44966937	ACTCCAGCCTGCTCA[-/AC]AGAGTGAGACCCAGA	54813
rs140932264	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44934006	GATTAAGTTTCCCAA[A/G]TGCCGGAAGTTCATT	54813
rs140984135	snp	A/T	0.00455668	0.047514	synonymous-codon	KLHL28	GRCh38.p7	14:44945608	TGCTGCTGGCAGGAG[A/T]GATTCAACTGTGTCC	54813
rs141051891	snp	A/G	3.54843e-05	0.00421199	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962480	CAGTCCTCTCTACCT[A/G]TCGGCTCCAGAGCCG	54813
rs141066196	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931873	CCTACTGCTGTGGAT[G/T]TGTGTAATCCTGAAT	54813
rs141122140	snp	A/G	0.000115362	0.00759393	synonymous-codon	KLHL28	GRCh38.p7	14:44945389	AACAATTTCATCCAA[A/G]TCAGCATGTGTAAGC	54813
rs141150917	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44935204	ACATAATGTTGAGAT[A/T]AAAAAGTCAAATTCA	54813
rs141155288	snp	C/G	4.95258e-05	0.00497599	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963276	TCAACAAATTGGGGA[C/G]CGACTTGGCCAAGAC	54813
rs141256462	snp	C/T	0.00358779	0.0422022	intron-variant	FAM179B	GRCh38.p7	14:44974738	TTAAAAAAGAGAATT[C/T]TTGATGCCTTTACCC	54813
rs141264940	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44951948	ACTGCAGCCTTGACC[C/T]CCTGGGCTCAGGTGA	54813
rs141272448	snp	A/G	0.0138799	0.0821421	intron-variant	FAM179B	GRCh38.p7	14:44966302	CATGGTGAAACCCCC[A/G]TCTCTACTAAAAATA	54813
rs141343918	snp	C/G	1.64868e-05	0.00287109	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963394	CCTTATTATTTGGAA[C/G]TTGAAGCCTCTGGAT	54813
rs141351294	snp	A/G	0.00914312	0.0669923	intron-variant	KLHL28	GRCh38.p7	14:44959496	AGAATTCACACTGAC[A/G]TTCAATATTCCTGGA	54813
rs141601576	snp	A/C	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44930086	AAAAAGAAACAGTTT[A/C]CTCCAATTTTTAAAG	54813
rs141673655	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926901	TTAATAATTTGATTG[C/T]TATAAACAAAGAAAA	54813
rs141963272	snp	A/G	3.29489e-05	0.00405874	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964029	AGAAGCTTTTGCCGT[A/G]TTGGCATCATCAATG	54813
rs141982460	snp	C/G/T	0.000971034	0.0220142	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962433	CTGCATGGCGGCTGC[C/G/T]CCCTCCGCGCTGCTT	54813
rs142049707	snp	C/G	0.000115398	0.00759512	synonymous-codon	KLHL28	GRCh38.p7	14:44945827	AAGAATGATGTCACA[C/G]AGTTCGTGATGTTGG	54813
rs142085632	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957418	CAAAATCACATAATT[A/G]GTAAAAAACATTACT	54813
rs142116819	snp	C/T	0.000760884	0.0194901	missense	KLHL28	GRCh38.p7	14:44934476	CTTTTTGGTCTAAAA[C/T]GCATATTCCAAATTC	54813
rs142154775	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44947727	TGAAATTTTTATCTT[C/T]GTCAAGTACGTAATT	54813
rs142281689	in-del	-/A	0.109814	0.206997	intron-variant	KLHL28	GRCh38.p7	14:44944477	TAAGTTATTGGGGGG[-/A]AAAAACATATTTCTT	54813
rs142335827	snp	A/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44971738	CGCAAATCTTGATAC[A/G]TTGTATTTTCATTTA	54813
rs142427628	snp	G/T	0.00716266	0.059414	intron-variant	FAM179B	GRCh38.p7	14:44975747	GCTGGGATTACAGAT[G/T]TGAGCCATCATGCCC	54813
rs142432436	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44972004	ACGTCTTACATGGCC[A/G]GAGAAGGAGGAAGAG	54813
rs142468409	snp	C/T	0.0150606	0.0854603	intron-variant	FAM179B	GRCh38.p7	14:44973394	TTGTAATTTCTTCCT[C/T]CCTGTCACCTGTTTA	54813
rs142524617	snp	A/G	0.000153988	0.00877328	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963246	AGAAGAATCTGAGAC[A/G]GCTTTCTCCGCACTT	54813
rs142562938	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44929704	TCCTTATAATAAAAG[C/T]AAGAGTTACTGAGGT	54813
rs142608471	snp	G/T	0.0130921	0.0798413	intron-variant	KLHL28	GRCh38.p7	14:44942846	AACTATCTTGATCGT[G/T]GCATAAACATTATGT	54813
rs142638956	snp	C/G	0.00676609	0.0577691	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961319	GGGGGCGGAGGTTAG[C/G]GGAGAGTCCCACAGA	54813
rs142703978	snp	A/C/T	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44940655	ACCCTTGCTTTCAAC[A/C/T]CCCCCGCCAGCCAGT	54813
rs142827733	snp	A/C	0.000182054	0.00953908	missense, intron-variant	KLHL28	GRCh38.p7	14:44931370	TCTACACACAGTCCA[A/C]TGATTTTGATGAGGA	54813
rs142828824	snp	A/C	0.00953873	0.0683987	intron-variant	KLHL28	GRCh38.p7	14:44954868	AATACAAAGGAAGAA[A/C]ATATCAACTTAGTGG	54813
rs142847555	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44933023	CTCAAGTTCCTTATA[C/T]AAAACAGTATAATAT	54813
rs142865643	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960359	TCAACTTGAAAATTC[C/T]GATCCAACATAAACT	54813
rs142921397	in-del	-/T	0.0111196	0.0737302	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925181	TGAGGTTATCACAAG[-/T]TTACTGAACTTTAAG	54813
rs142959695	snp	A/G	0.00676609	0.0577691	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924947	TTGTATTAAAAATGT[A/G]TTGTATTCCTCACTC	54813
rs143015273	in-del	-/T	0.0778436	0.181279	intron-variant	FAM179B	GRCh38.p7	14:44973241	TTATGCTGCTGCTCC[-/T]TTTTTTTTTAAATTA	54813
rs143163214	snp	A/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44974488	TTCAACATTCCTGCC[A/G]TATCCAATTCTAGTT	54813
rs143278133	snp	A/G	0.0130921	0.0798413	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937443	TGATCCACTGTGCCC[A/G]GCCCAGAATTGAATT	54813
rs143328012	snp	A/G/T	0.00108738	0.023292	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963915	TTGCATCTGCTCCCT[A/G/T]CTGACCTATCCTAGT	54813
rs143357572	snp	A/G	0.00120788	0.0245455	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963535	AACCGGACCCAGGCC[A/G]TCGAAGAACTAAAGC	54813
rs143405736	snp	A/G	0.00597247	0.0543191	intron-variant	KLHL28	GRCh38.p7	14:44947634	CCATCAATTCTATAA[A/G]TTCAAACATTTTGAA	54813
rs143435451	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939159	GCCACAGCTGGGGAA[A/G]CTACACTAGAATGTG	54813
rs143524307	snp	G/T	0.000153988	0.00877328	missense, intron-variant	KLHL28	GRCh38.p7	14:44931346	ACCTGTTCTAGGTTC[G/T]TTCATTGGTCTACAC	54813
rs143583376	snp	A/G	0.00107347	0.0231426	synonymous-codon, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929163	ACCGACGACATAAAG[A/G]TAGTTATCGATTACA	54813
rs143839034	in-del	-/TCT	0.0103295	0.0711199	intron-variant	FAM179B	GRCh38.p7	14:44975933	CCATGATTTATAAAA[-/TCT]TCTTAGTGAAGTCAA	54813
rs144010175	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967721	ACTGGAGATGTAGAT[A/G]GGGTAAAGTATGGAG	54813
rs144072860	snp	G/T	0.00835141	0.0640778	intron-variant	FAM179B	GRCh38.p7	14:44966763	GTTCGAGACCAGCCT[G/T]GGCAACATAGTGAGA	54813
rs144227970	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44942002	CATACCTCTAAACTA[C/T]ACTATATGCTGATGA	54813
rs144286123	snp	C/T	0.00318978	0.0398085	intron-variant	KLHL28	GRCh38.p7	14:44938263	TTTACTTCCAAAACA[C/T]AATGGTGAGAAAGGC	54813
rs144288954	in-del	-/AA	0.106633	0.204807	intron-variant	KLHL28	GRCh38.p7	14:44938371	AACAAGGAAAACATT[-/AA]GTCTTCTTTTTTTTT	54813
rs144296967	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955643	ATAAAAAAATTAGCT[A/G]GATGTGGTGGCACAT	54813
rs144384782	snp	A/G	0.00517822	0.0506191	intron-variant	KLHL28	GRCh38.p7	14:44931118	CAAGTTTGAGAAACA[A/G]TAATATGCACATTGG	54813
rs144393904	snp	A/C	0.00953873	0.0683987	intron-variant	KLHL28	GRCh38.p7	14:44956159	AGAGATAGGGTCTTG[A/C]TACCTTGCCGAAACT	54813
rs144462101	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44950429	TCACATAGTGATAGA[A/T]CCTATATTGTTAACC	54813
rs144547466	in-del	-/TC	0.0640965	0.167152	intron-variant	KLHL28	GRCh38.p7	14:44958731	ATGTTATGACAGGCG[-/TC]TAAGTTACATAATTA	54813
rs144653789	snp	A/G	0.000906656	0.0212722	synonymous-codon	KLHL28	GRCh38.p7	14:44945842	GAGTTCGTGATGTTG[A/G]CGAAGAAGATTCAAG	54813
rs144734587	snp	C/T	1.65094e-05	0.00287305	stop-gained, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963277	CAACAAATTGGGGAG[C/T]GACTTGGCCAAGACA	54813
rs144808434	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44929727	ACTGAGGTGAGAGGA[C/T]GGCTGGAGGCCAAAA	54813
rs144826840	snp	C/T	1.648e-05	0.0028705	synonymous-codon	KLHL28	GRCh38.p7	14:44945698	ATCAATGCATTGAAA[C/T]TCAACCTCACTGTTC	54813
rs144833686	in-del	-/TAA			intron-variant	FAM179B	GRCh38.p7	14:44979172	CCTATAAGTCACCAT[-/TAA]TAATAATAATAATAA	54813
rs144839266	snp	A/C	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44976555	ACAGTGCTTGGCACA[A/C]AGGAGGCACTTGAAG	54813
rs144860260	snp	C/T	3.29652e-05	0.00405974	missense	KLHL28	GRCh38.p7	14:44934419	GTTTTCTGATAGTGA[C/T]GCCAGGACGCACATT	54813
rs144953412	snp	C/T	0.00517822	0.0506191	intron-variant	KLHL28	GRCh38.p7	14:44956978	GCATGCTACCATGCC[C/T]GGCTAATATTTTTTA	54813
rs144954711	in-del	-/T	0.100231	0.200173	intron-variant	FAM179B	GRCh38.p7	14:44967925	ATCTGGTAGTGATGA[-/T]TTTTTTTTAAGGCAT	54813
rs145093890	snp	A/C	0.0115144	0.0749975	intron-variant	KLHL28	GRCh38.p7	14:44950164	TTAAACGAGTTTATA[A/C]ATAAAAAGGGCTCAG	54813
rs145159377	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928905	AACAAAACTTTTGAG[A/C]CTTCATGCTACTTCA	54813
rs145441267	snp	A/G	0.000153988	0.00877328	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963081	GAGAACGCTTATACA[A/G]CAAGGACTGGAAAGT	54813
rs145492514	snp	A/C	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44975054	TTTAACAAAGAGATT[A/C]TTGCTTCCTTTACCC	54813
rs145536288	snp	A/C	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44978042	AATTGCTAACATGAG[A/C]TTTTGAGGATAATTG	54813
rs145550307	in-del	-/T			frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963536	CCGGACCCAGGCCGT[-/T]CGAAGAACTAAAGCA	54813
rs145606315	snp	A/C	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44979469	GAGCCCTCATGACCT[A/C]ATCACCTCCCAAAGG	54813
rs145607166	snp	A/C	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44973225	CTTTCTTAGCATATC[A/C]GTTATGCTGCTGCTC	54813
rs145693290	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974168	CACGTTTTGTAGTTT[C/T]CCCACAGTTCTTGTA	54813
rs145822863	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954717	ACTAAAAACTAGAGG[A/G]TAGAGATAGAAGGTA	54813
rs145888351	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940264	TTAAAGGCCCCATCT[C/G]TTAACATTGTTCCAA	54813
rs145902696	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958232	GCTCTGAAACCAAGT[C/T]AATAAAGGTCAAGTT	54813
rs145930061	snp	C/T	0.00597247	0.0543191	intron-variant	FAM179B	GRCh38.p7	14:44971928	ATTGACTCATAGTTC[C/T]TCATGGCTGGGTAGA	54813
rs145970760	snp	A/G	0.00438332	0.0466095	intron-variant	FAM179B	GRCh38.p7	14:44975833	TTTTCAAGTGACTCA[A/G]AACAACACAGCTTTG	54813
rs146086725	snp	C/T	3.30458e-05	0.0040647	missense, intron-variant	KLHL28	GRCh38.p7	14:44931401	TCGTATCTTTCAATG[C/T]TGGACAAATGTGAGA	54813
rs146213742	snp	A/C	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44967481	AGAATTTTGTGGTCA[A/C]ACTTTTCTTAAATTA	54813
rs146329724	snp	C/T	0.00358779	0.0422022	intron-variant	KLHL28	GRCh38.p7	14:44947736	TATCTTTGTCAAGTA[C/T]GTAATTGTTTCATAC	54813
rs146334475	snp	A/G	0.222333	0.248464	intron-variant	KLHL28	GRCh38.p7	14:44941443	TCGAGACCAGCCTCA[A/G]CATGGAGAAACCCTG	54813
rs146425772	snp	C/T	0.00469254	0.0482105	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964437	AATCATGGGAGAAAA[C/T]CAGACCTCCACTTCC	54813
rs146515749	snp	A/G	0.000659979	0.0181536	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963263	CTTTCTCCGCACTTC[A/G]ACAAATTGGGGAGCG	54813
rs146579363	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44973436	CATTTCATTTATACA[G/T]AAACACACAGACACA	54813
rs146629695	snp	A/G	0.00597247	0.0543191	intron-variant	FAM179B	GRCh38.p7	14:44967841	ATCCCAAAACTTGTA[A/G]ATTTTTTTGGAAATA	54813
rs146638221	snp	A/C/G	0.000349228	0.0132098	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962557	ATTATGAGAGGAGAG[A/C/G]AAAACTACTACTTCC	54813
rs146653759	snp	A/C	0.0130921	0.0798413	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962370	TGGGCTCCATCGAGC[A/C]CTTTGGAGACGGCAA	54813
rs146726595	snp	C/G/T	0.000165115	0.0090846	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963468	CAATCTTAAATTTGG[C/G/T]ATTATTCCTCAGGAG	54813
rs146754789	snp	C/T	0.00358779	0.0422022	intron-variant	KLHL28	GRCh38.p7	14:44942256	TCTTCCTCATCATCC[C/T]TCCCTCATATCCATT	54813
rs146776860	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939111	CTTGTGCCTTCTAGA[A/G]TAGCAGCCTGAGCCA	54813
rs146938471	snp	G/T	0.00755907	0.0610114	intron-variant	KLHL28	GRCh38.p7	14:44946272	AGTCTGAGCTATCAC[G/T]GAAATAAAATGAAAA	54813
rs146962187	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44951977	GATTCTCCCACTTCA[A/G]CCTCCCAAGTAGCTG	54813
rs147052510	snp	A/G	0.00438332	0.0466095	intron-variant	FAM179B	GRCh38.p7	14:44969215	GCTGGAGTGCAGTGC[A/G]ATCTCGGCTCACTGC	54813
rs147146800	snp	A/T	0.0150606	0.0854603	intron-variant	KLHL28	GRCh38.p7	14:44936815	GTGATGTTTCTCGAA[A/T]CTAAGCTAGGCAAGA	54813
rs147289430	snp	G/T	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44978394	ACATATATATAAAAA[G/T]GAGATTTTTGTGCCT	54813
rs147432661	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960573	CCCTAAAATGAAACA[C/T]GCTAGCTAAACCTAA	54813
rs147498061	snp	G/T	0.000131859	0.00811862	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963934	ACCTATCCTAGTGAG[G/T]ATTTTGACTTGCCCA	54813
rs147521605	snp	C/G	3.31846e-05	0.00407323	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962594	CTGCGGGGGACCACG[C/G]TTCCTGCCCCACTAC	54813
rs147534166	snp	C/T	0.00358779	0.0422022	intron-variant	KLHL28	GRCh38.p7	14:44940938	AACCCTGTTTCTACC[C/T]AAAATACAAAAATTA	54813
rs147541463	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937550	TAAAGGTTATGATGA[C/T]GGATTATCTGTAAGT	54813
rs147583402	snp	C/T	8.24899e-05	0.00642169	synonymous-codon	KLHL28	GRCh38.p7	14:44934459	ACCACCTATAACATA[C/T]ACTTTTTGGTCTAAA	54813
rs147792270	snp	G/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44951614	TGGGCCAAAGAAAAG[G/T]CACTGGTAAAAGTAA	54813
rs147808879	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44943964	AAGTGATCCTCCTGT[A/G]TTGGCCTCCCAAAGT	54813
rs147815198	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44956166	GGGTCTTGCTACCTT[A/G]CCGAAACTAGTCTCA	54813
rs147901806	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926817	CCGTCCTAAAATCAT[G/T]TTCCACAGTCTTTCA	54813
rs147938667	snp	A/G	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44932328	AAAGCAATCACTGTA[A/G]ATTGCATAGTACAAA	54813
rs148018330	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936778	GCAAAGGGGCCATGG[C/T]GTATTTAAAGGAATG	54813
rs148092859	snp	A/G	1.66346e-05	0.00288393	synonymous-codon	KLHL28	GRCh38.p7	14:44945908	GTTAGCAAGCATGTA[A/G]GTCGGGGATGTGTGG	54813
rs148179767	snp	C/T	0.0142736	0.0832652	intron-variant	KLHL28	GRCh38.p7	14:44941093	CAACAAAGTGAGACA[C/T]CTGGGCGACAGAGCG	54813
rs148283501	snp	A/G	0.0111196	0.0737302	intron-variant	FAM179B	GRCh38.p7	14:44974688	ACACTTTTGATGAGC[A/G]TAATTTTATGGTTGG	54813
rs148321239	snp	C/T	0.000181484	0.00952412	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963788	TCAAACAAGAATACA[C/T]GAAAATCTTCCTCAA	54813
rs148339331	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947701	TTTTTAAGTGGAAAA[A/T]ATCCAACTCTTGAAA	54813
rs148407295	snp	A/G	0.00517822	0.0506191	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924509	TGATGCTAAAAAGGT[A/G]CATGTTCAGAGGTAA	54813
rs148593600	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44976943	TAAACCTAAAAATTA[A/G]TATTTTAAAAATACC	54813
rs148617472	snp	A/T	0.00438332	0.0466095	intron-variant	FAM179B	GRCh38.p7	14:44971987	GTGAAGAGGAAGGAG[A/T]CACGTCTTACATGGC	54813
rs148819135	snp	A/G	0.00102084	0.0225695	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963100	GGACTGGAAAGTACC[A/G]ATGCCCGACTTAGAG	54813
rs148877153	snp	C/G	0.00874735	0.0655527	intron-variant	KLHL28	GRCh38.p7	14:44936670	TAAAATGGGTATGTA[C/G]GTTTCTCCAGTTACA	54813
rs148909555	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44942497	TCTAATAATTTCACT[A/G]ACCTCCTTAGAATGG	54813
rs149031215	snp	C/T	0.00636936	0.0560724	intron-variant	KLHL28	GRCh38.p7	14:44957413	ATTAGCAAAATCACA[C/T]AATTAGTAAAAAACA	54813
rs149068365	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940222	AATCCCTTCATGAGA[A/G]CAGAGCCCTCATGGC	54813
rs149139757	snp	C/T	0.00241254	0.0346475	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929009	TCACCACCATACTAT[C/T]TCCGAGAGTTCACAT	54813
rs149300159	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971199	ACTCTGGTGCTTTCT[C/G]TTTTGGAAGGTTATT	54813
rs149344935	snp	C/T	0.00358779	0.0422022	intron-variant	KLHL28	GRCh38.p7	14:44959940	AAATCTGCTTCGTAA[C/T]AAAAAGAATACACAC	54813
rs149459937	snp	A/G	0.00318978	0.0398085	intron-variant	KLHL28	GRCh38.p7	14:44931043	GACATTTGTTACATG[A/G]ACAAAAGGAGCTTCT	54813
rs149503839	snp	A/C	0.0998734	0.199905	intron-variant	FAM179B	GRCh38.p7	14:44966253	GAGGCAGGCAGATAA[A/C]CTGAGGTCAGGAGTT	54813
rs149557242	snp	A/G	0.000153988	0.00877328	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963722	TACAGCAGTTCTTGG[A/G]ACCAGTTATAGCAGC	54813
rs149661832	snp	A/G	0.0174175	0.0916809	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962225	CCCGGTGGCAGCTGT[A/G]GGGTCTAGGGCTCAG	54813
rs149856079	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968814	TCAGTACATTCTGTG[A/G]GGTTTTGACAAATGT	54813
rs149875466	snp	A/G	0.000148267	0.00860879	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964147	GCCAGATTGGCTAGG[A/G]AAACCTTACCAAGGC	54813
rs149949889	snp	A/G	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44950086	ATCACATGAAAAACC[A/G]AGGAATGAAGGTTAC	54813
rs149995293	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44978923	AGGATCATTTGAGCT[C/T]AGGAGTTCAAGGCCA	54813
rs150046906	snp	C/T	0.00914312	0.0669923	intron-variant	KLHL28	GRCh38.p7	14:44938197	CAAGGCATGATACAT[C/T]CTGAGGCAAATTCCC	54813
rs150062543	snp	C/T	0.00207469	0.0321409	missense	KLHL28	GRCh38.p7	14:44934251	GAATGTACTTCTCTA[C/T]AGATTGTAAATAAGA	54813
rs150172110	snp	C/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44970670	TGATGTTATCTGTAT[C/G]CTTTCTTGTAGTGTT	54813
rs150208188	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44959583	TAATGTGTTATCTCT[C/G]ATTCTGGAAATAAAG	54813
rs150361630	snp	C/T	0.00557542	0.0525036	intron-variant	KLHL28	GRCh38.p7	14:44939656	GATGGCCTTTACTCT[C/T]AGTTTCTGCTTGAGA	54813
rs150379775	snp	C/G	0.000362611	0.0134601	missense	KLHL28	GRCh38.p7	14:44945459	TGGCATATGTATTTA[C/G]TGGCTGCCAAATAAA	54813
rs150433582	snp	C/T	0.000307953	0.0124049	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963545	AGGCCGTCGAAGAAC[C/T]AAAGCAGGTGCTGGG	54813
rs150435215	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44964886	AATTCGTTAAGTGCT[A/G]AAGTAGAAATATAAA	54813
rs150534843	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961336	GAGAGTCCCACAGAG[A/G]AACTGCATTAGAAGG	54813
rs150623925	snp	A/G	0.0130921	0.0798413	intron-variant	KLHL28	GRCh38.p7	14:44948975	GGAGAATGGTAGACT[A/G]AAAAGTGAAGGATGA	54813
rs150689217	snp	C/T	5.59937e-05	0.00529091	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962434	TGCATGGCGGCTGCC[C/T]CCTCCGCGCTGCTTC	54813
rs150751408	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44930420	CAGGCATGTGCCACC[A/G]CACCAGGCTAATTTT	54813
rs150835238	snp	A/G	0.000164837	0.00907697	missense	KLHL28	GRCh38.p7	14:44934199	CAACTTCTTGTTGTC[A/G]TCATTGGTGCCACAG	54813
rs150924609	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44952380	TCAGAAACTACATAG[A/G]GCAGTGGGGTTGCAG	54813
rs151066226	snp	C/T	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44933389	ATTCAAGGCTCACTG[C/T]AGCCTCAACCTCCTG	54813
rs151117139	snp	A/C	0.00199481	0.0315187	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924968	TTCCTCACTCTTTTC[A/C]AATGTGTATCAACAC	54813
rs151146395	snp	C/T	1.64825e-05	0.00287071	missense	KLHL28	GRCh38.p7	14:44945369	ACATTCAAACAGTCA[C/T]TGGAAACAATTTCAT	54813
rs151276572	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44978764	ATCATAGTGTCACTG[C/T]ACACTAGCCTGGGAG	54813
rs151319864	snp	A/G	0.00318978	0.0398085	intron-variant	KLHL28	GRCh38.p7	14:44957909	TCCAGAGGATAGATC[A/G]TTCATATAAAATCTT	54813
rs151329107	snp	A/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44972415	TTGTTGAGTTCAACT[A/G]TGTCTTTACTGATTT	54813
rs180773730	snp	A/G	0.00755907	0.0610114	intron-variant	KLHL28	GRCh38.p7	14:44953909	AAATCGTAAGTAAAA[A/G]TATAAATGAGACTGA	54813
rs180787004	snp	C/G	0.00398564	0.0444627	intron-variant	FAM179B	GRCh38.p7	14:44965024	TTGAACTGAGATTTT[C/G]CCCCCAAAGCTTTTA	54813
rs180803983	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44943442	GCAGGTGGATCACCT[A/G]AGGTCAGGAGTTTGA	54813
rs180810829	snp	G/T	0.0023933	0.0345097	intron-variant	KLHL28	GRCh38.p7	14:44932012	TACAGACTTTTTTTT[G/T]TTGTTCCTAAATTTT	54813
rs180874535	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44971708	TTTCCTCTAGGCACC[A/G]CTTTCACTGCATACC	54813
rs180880103	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948823	ATTCAAATTCTCAAA[A/G]CTCAAGATCAAAAAT	54813
rs180880551	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926856	TATCTTTTGGGAATA[C/G]GGGATTAAAAATAGT	54813
rs181041185	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44937854	GCCGGACTTATCCTT[C/T]TATTAAGAGCCCACT	54813
rs181053515	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958296	TAAGCCACAAAACAG[C/T]GGTGCTGAAATCAGT	54813
rs181090514	snp	A/G	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44953247	ACGGAATAGCCATAT[A/G]GAAACAGGTAAAACT	54813
rs181092566	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974385	ACGCTTCATGACTTA[C/T]ATTATCCTTTTGTTC	54813
rs181100001	snp	C/T	0.00318978	0.0398085	intron-variant	KLHL28	GRCh38.p7	14:44931255	TCCTACTGCTATATT[C/T]CAAGGAACTATTATT	54813
rs181163258	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944079	TGGAAAGGGAAAAGC[A/C]ATCTACCAAATTTTT	54813
rs181636249	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44965905	TTTGAGATGGAGTCT[C/T]GCCCTGTTGCCCAGG	54813
rs181659611	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948034	GTTATTCCAGTGTTG[A/G]TCTTTTTAACCTATG	54813
rs181689486	snp	A/T	0.00318978	0.0398085	intron-variant	KLHL28	GRCh38.p7	14:44929943	TAGGCTATTTTTTTT[A/T]AATTTCATTTCATTC	54813
rs181715347	snp	C/G	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44971239	GTTTCTTTACAGATA[C/G]AGGCCTAGTCAGATT	54813
rs181761692	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925397	ATACATTATCCAATT[C/T]TAGGAGATTTGGAGT	54813
rs181822892	snp	A/C	0.00358779	0.0422022	intron-variant	KLHL28	GRCh38.p7	14:44959266	CACCCATAAAATGTT[A/C]CATAGTCCAAATGTA	54813
rs181833294	snp	C/T	0.00716266	0.059414	intron-variant	KLHL28	GRCh38.p7	14:44938485	CACACCATTCTCCTG[C/T]CTCAGCCTCCCGAGT	54813
rs181838411	snp	A/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970154	AGCTTGACAATATTG[A/T]GTCTTCCTATCCACA	54813
rs181875073	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44943783	GCAATGGTGCATTCA[C/T]AGCTCACTGCAACTT	54813
rs181925280	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924921	CACCAGTAGGAAAAT[C/T]TGTAAACCTATTGTA	54813
rs182186245	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967937	ATGATTTTTTTTAAG[A/G]CATTACTCTTAAGAC	54813
rs182196812	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944588	CATTTCTTTGGTAGC[A/G]CTTCTAGTGAACTGT	54813
rs182280582	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44947304	AAGAACAGATTCTCC[C/T]GTAGAGCTTATGGAA	54813
rs182380444	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44972546	GCCTCATTTAATTTG[A/G]CACTGTTGTTGGGCA	54813
rs182540088	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44932743	CAAGATAATCAAATT[C/T]AAAATACTTAACCTT	54813
rs182546924	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44956634	TCTTCAACAAATAAA[C/T]TGCAAGAAATAAAGA	54813
rs182591801	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940158	GACTTATCTTATTAT[C/T]AGGAGCCCACTCCTG	54813
rs182782993	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44977531	GTGAGCCACAGCACC[C/T]GGCCAAGACTGACTT	54813
rs182802127	snp	A/C	0.00835141	0.0640778	intron-variant	KLHL28	GRCh38.p7	14:44956259	AGCCACTACACCTGG[A/C]CAAATTTCTCTTTTT	54813
rs182803895	snp	C/T	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44976862	CTTCAGAAATAGTTT[C/T]GATGTCAGTTACTCC	54813
rs182873812	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961005	TTATTCCTTCAAAAA[A/C]AAAAAATATCTCTTC	54813
rs182946968	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939285	ACTACAACGGGAGGT[A/G]CAGCCTCAAAGATCT	54813
rs183030243	snp	G/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44960051	TAAATATCCACTATG[G/T]AGACTAATGCCTCTT	54813
rs183032983	snp	A/C/T	0.00159617	0.0282053	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927776	TACCTAAGAAATGTA[A/C/T]AAAGTAATGCATAAC	54813
rs183061909	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44932544	CACAAAGGCACAGAG[A/G]TAAGATTGTTGGGCT	54813
rs183063919	snp	C/T	0.00953873	0.0683987	intron-variant	KLHL28	GRCh38.p7	14:44954857	TGAAAATTGAAAATA[C/T]AAAGGAAGAAAATAT	54813
rs183398061	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961373	TTTGATAACGTCTAA[A/G]GGAGAGGCGGTTAGC	54813
rs183411626	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950850	TTGCCAACTATATCC[A/G]TGAAATGCCTTTCCA	54813
rs183415004	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44940971	CGGGTGTGGTGGCAT[A/G]TGCCTGTAATCCCAG	54813
rs183435752	snp	C/G	1.76749e-05	0.00297273	intron-variant	KLHL28	GRCh38.p7	14:44944983	CTGCACATTTAAAAA[C/G]CATAAAATCAATTAG	54813
rs183454952	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44976164	TTCATTGGCTCCAAC[A/C]ATCTTCAAGATAAAA	54813
rs183631164	snp	G/T	0.00835141	0.0640778	intron-variant	FAM179B	GRCh38.p7	14:44972276	AAAGTGTGTGTGTGT[G/T]TTTTTTTTGCGATAG	54813
rs183651278	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44970009	TTCCTTCCATGTTGA[A/G]TTCACTCTTCTGGGT	54813
rs183690344	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968656	CCTGACCCACCTCAT[C/T]CGGTACTTTAGGGGT	54813
rs183697899	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44971845	ATGTTGGGGTTTTCC[A/G]TCTGTATTCTGTTCT	54813
rs183706475	snp	C/T	0.00398564	0.0444627	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927465	ACTTTATAAGGAGAT[C/T]GCAAACAGGTTTAAA	54813
rs183742287	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946940	AAAAAGAATAAAAAT[A/G]GCAGGGAAGAAAAGG	54813
rs183746017	snp	C/G	0.00478085	0.0486577	downstream-variant-500B	KLHL28	GRCh38.p7	14:44924266	ATAAAACCCTAAGAG[C/G]TGAGCATGACAAAGT	54813
rs183784511	snp	A/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928592	CATCCAAGAAGCAGT[A/T]TCAGCACTCTGTCCA	54813
rs183879350	snp	G/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44951347	GTGTCAAGCCACGGA[G/T]AAGCTGCAGTCCTGA	54813
rs183912130	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44949546	TTAATGGAATGAGGC[C/T]TAGAGGGATGCTTCT	54813
rs184081323	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958067	ATATCTCTGCCATAG[A/T]TTTTGTTCTTTTTTT	54813
rs184202065	snp	G/T	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44952435	TCCTCCAGGTTATTC[G/T]TAGGCAAAAGTTCCA	54813
rs184205401	snp	A/T	0	0	intron-variant	KLHL28	GRCh38.p7	14:44930625	TGTTCACTTAAGCAT[A/T]TCACACTTTAGATTT	54813
rs184300474	snp	G/T	1.65811e-05	0.00287929	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963653	CTAACTTCAAAGTGG[G/T]GCATGGCACACTTGA	54813
rs184411921	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44978176	ATAAAAGTAGTTTGA[A/G]AATCATGAAGAGTTA	54813
rs184417766	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957254	TGCGTGATAGGTAAA[C/T]AGATGTTCATCATAT	54813
rs184420929	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44935170	ACTATAGCTACATGT[C/T]GCTGGGGGAATCTTA	54813
rs184431139	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942848	CTATCTTGATCGTTG[C/T]ATAAACATTATGTAT	54813
rs184562366	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44964809	TAAATTCTGGGAATG[A/G]AGATGAGGCCAGTTT	54813
rs184888850	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971799	TTTCTTTGACTTGTA[C/T]GTAACTTAGAAGTGT	54813
rs184891433	snp	A/G	0.00279162	0.0372561	intron-variant	FAM179B	GRCh38.p7	14:44969339	TGTATTTTTAGTAGA[A/G]ACGGGATTTCACCAT	54813
rs184898308	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44949150	CATTACCAGTGCCAC[A/G]GGACTGAAGACTATT	54813
rs184905315	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927040	TTTATTCAAATCAAT[A/G]AAAAAGTTATTGCTA	54813
rs185013773	snp	A/G	0.0209421	0.100162	intron-variant	KLHL28	GRCh38.p7	14:44943487	ACATGGTGAAACCCC[A/G]TTTCTACTAAAAATA	54813
rs185019612	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946069	TCATAGTAAATACTA[C/G]AACTAGAGGCTTTCA	54813
rs185103692	snp	C/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44965028	ACTGAGATTTTCCCC[C/G]CAAAGCTTTTATTTA	54813
rs185109266	snp	A/C	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44973832	TTAAATATTCCAATC[A/C]ACTTTCTTCTTCTTT	54813
rs185135136	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44953285	TGCTACATACCTACA[C/T]CAACAGGATAAATTA	54813
rs185136888	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975091	GTGTATATTTTTTAT[A/G]TACCAGAAAGCAATA	54813
rs185149774	snp	C/T	1.80309e-05	0.00300252	intron-variant	KLHL28	GRCh38.p7	14:44931545	TAACGCTCCACACTG[C/T]AAATATTTAAAAAAA	54813
rs185240804	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44947784	TTAAGTCAGTTAATA[A/T]ATTATGTTAATATGG	54813
rs185250133	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44941797	ACACACAAATTCCTT[A/G]GCTTTTATGACTCTA	54813
rs185353701	snp	A/G	0.00318978	0.0398085	intron-variant	FAM179B	GRCh38.p7	14:44970599	GCAGTGATGAGAGAG[A/G]ACATCCTTGCCTTGT	54813
rs185361638	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925075	AATTAAAGTGCTGTT[C/T]ACAAAGGGAAAAAAG	54813
rs185574125	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44925636	AGCTCCCACAGCATC[C/T]AACAGAATATCTCAT	54813
rs185658551	snp	A/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44948059	CCTATGTAACTTCTT[A/T]TAGCCTCAGTTTTAT	54813
rs185659567	snp	G/T	0.00597247	0.0543191	intron-variant	FAM179B	GRCh38.p7	14:44972912	ATTTTGCTATAATGT[G/T]GATGAGGAAAAAAAT	54813
rs185680083	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44929462	CATAACTTTTATTAC[A/G]ATATATTGTTACAAT	54813
rs185788919	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958682	ATGTGGTAATGACTT[G/T]GAACTTGCTTTCTTC	54813
rs185809601	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952045	TGTATTTTTTTTGTA[C/G]AGAAGGAGTTTCACC	54813
rs185904325	snp	C/T	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44954872	CAAAGGAAGAAAATA[C/T]CAACTTAGTGGCCTT	54813
rs185904595	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932573	CTTGTTCTGGCCCTA[A/C]CCTATTTCCTGAAAA	54813
rs185918270	snp	A/C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44938057	CTGGCCCTCAAAATT[A/C/T]GTGTCCTTCTCACAT	54813
rs185992625	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44976245	GCCCTATCCTTATTC[A/G]TTGCCTATCTACATT	54813
rs186155336	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44938616	ACCTCGCGATCTGCC[C/T]GCCTTGGCCTCCCAA	54813
rs186306253	snp	C/G	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44944116	GGTCAGAAATCCACA[C/G]TATTAAAAAATATGT	54813
rs186392533	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44959578	GGAACTAATGTGTTA[C/T]CTCTGATTCTGGAAA	54813
rs186519782	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44971259	CTAGTCAGATTATCC[A/G]TATCTTCTTGTGTGT	54813
rs186520779	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939668	TCTCAGTTTCTGCTT[C/G]AGACCTCATCAGAAT	54813
rs186559718	snp	A/C	0.00517822	0.0506191	intron-variant	FAM179B	GRCh38.p7	14:44966033	GCTCCCACCACCACG[A/C]CCAGCTAATTTTTGT	54813
rs186665778	snp	C/T	0.00398564	0.0444627	intron-variant	KLHL28	GRCh38.p7	14:44951389	TTGCCTACATGGATA[C/T]ATGCAAGGTGACCAG	54813
rs186665960	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44972799	ACAGCCTATATAGTA[A/G]TTACTCATTTAAGTT	54813
rs186737309	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44960053	AATATCCACTATGGA[A/G]ACTAATGCCTCTTCT	54813
rs186786335	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943907	TTTTTGTAAGGACAG[G/T]ATCTCGTTATAATGC	54813
rs187072394	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44946507	AGTCCCATGAGGGCA[A/G]TAAGGCTCACTTACT	54813
rs187076629	snp	A/G	0.0023933	0.0345097	intron-variant	FAM179B	GRCh38.p7	14:44977312	TGATCTCAGCTCACT[A/G]CAAGCTCCACCTTCC	54813
rs187085162	snp	C/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44956404	AGCTAGATAATTGGG[C/T]CTTCTGATGGAAAAA	54813
rs187204678	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44972297	TTTGCGATAGAACGT[A/G]GTATTTCTTTGTTAG	54813
rs187313725	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44950983	AGCCATTTTAAAATA[C/T]AGATGGCTTATTAGA	54813
rs187317062	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928185	AAAAAATTAATATGC[A/G]CTAAGAATGGTACTA	54813
rs187385668	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975509	TTTCACTCTGTTGCC[C/G]AGGCTGGAGTGCAGT	54813
rs187413194	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932298	CGTCACAGGAGAATT[A/C]ATGTGGCTTACTGCA	54813
rs187507956	snp	A/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928689	AGAGCTAAAATAAAA[A/T]AAAAAAAAAAAAAAA	54813
rs187650249	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962208	TGGTGCCCTTGGTTA[A/C]GCCCGGTGGCAGCTG	54813
rs187665672	snp	A/C	0.0322114	0.122752	intron-variant	KLHL28	GRCh38.p7	14:44954224	AGGTAAATCTGTCAA[A/C]ATACAGCAAAATTAC	54813
rs187680855	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941253	TTCTTAAAAGAAAAG[A/T]CTTCATTCAGTTTAT	54813
rs187764566	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44940343	TATAGCAGAGGGCAA[C/T]AATAATCAGTTCTAA	54813
rs187905178	snp	G/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44968299	GAGTTTCACTCTGTC[G/T]CCCAGGCTGGAGTGC	54813
rs187919607	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44944662	TTCCTAGTTCTCTTC[C/T]TTGCTATCTTCTGAT	54813
rs188150082	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943048	ATGCAAATAATACTT[C/T]TAATTTTTAAAATTT	54813
rs188192202	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44933309	TCTTTTCTTTTCTTT[C/G]TTTCTTTTTTTTTTT	54813
rs188253941	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969442	CAGGTGCAAGCTACC[A/G]CGCCTGGCCTATCAG	54813
rs188259891	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968867	TATAGTATCATAACA[A/G]TAGTTTCAGTGCCCT	54813
rs188283294	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44975175	ATGTTTTCATTAGCC[A/G]CTTTGACACAGATCA	54813
rs188299008	snp	G/T	0.000280419	0.0118377	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963796	GAATACATGAAAATC[G/T]TCCTCAAGCTAATGA	54813
rs188557770	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44974155	TATACATATGTTACA[C/T]GTTTTGTAGTTTTCC	54813
rs188563216	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44953097	AGGATTAAATGAGAC[A/G]TATGTAAGGAAAAAT	54813
rs188565508	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44930844	TTCAAAGATAACAAT[G/T]TTTCCTAAACCACAA	54813
rs188711762	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44949898	ACTACAGAGGAGAAA[C/T]TTTTGCTTTGCTCTG	54813
rs188798048	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44957481	TGCTCTCTACACATT[A/G]CATACAAAAAATTAA	54813
rs188800183	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44979140	CTTGACATAAATTTT[G/T]TATCCCTAATTTGCT	54813
rs188802948	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977898	CAAGCAATCCTCCCT[C/T]CACTGCCTCTGAAAG	54813
rs188816163	snp	C/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44935270	GAATCTCTGGATTAG[C/G]AATGAAGATAGTGGT	54813
rs188821590	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44934985	ATGTGTCCTGTCTGA[A/G]CAACTCTACTGATGA	54813
rs188973890	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44971929	TTGACTCATAGTTCC[G/T]CATGGCTGGGTAGAC	54813
rs188992033	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927620	AAGTTAAACACTTTC[A/T]TTAAATAAGCTGTCA	54813
rs189102322	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44956690	GTATCAATCAAATAC[A/G]ACCTGTGAACCATAG	54813
rs189309471	snp	A/T	0.00279162	0.0372561	intron-variant	KLHL28	GRCh38.p7	14:44931784	GCAAAGTATATTAAG[A/T]GCATAGAACTTGGAG	54813
rs189316242	snp	G/T	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44964865	CCTGGGAATTAGCAG[G/T]TAACAAATTCGTTAA	54813
rs189429017	snp	C/T	0.00755907	0.0610114	intron-variant	FAM179B	GRCh38.p7	14:44965828	ATCCACCAATGGTCT[C/T]TACCTGTATCATTTA	54813
rs189446233	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943560	TACTTGGGAGGCTGA[A/G]GCAGGAAAATCACTT	54813
rs189488684	snp	A/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44970140	TGAGAAAAACTAACA[A/G]CTTGACAATATTGAG	54813
rs189496978	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44947283	TCACCAGAAGCTAGA[A/G]GAGCCAAGAACAGAT	54813
rs189498854	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924512	TGCTAAAAAGGTACA[C/T]GTTCAGAGGTAAAAT	54813
rs189546506	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958193	AAATAAAACTTTCCA[C/T]AGTCTACAGTAACTT	54813
rs189590489	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44953886	CATTTTAAAAACTTG[A/G]AATAAAGAAATCGTA	54813
rs189815240	snp	G/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44967102	ATTTGAAAACAAAAG[G/T]CTGAGTATAGATTTG	54813
rs189825723	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44944516	CTTTTAAAAATACAC[C/T]GAAGAAAACAAATTA	54813
rs189837475	snp	A/G	0.00199481	0.0315187	intron-variant	KLHL28	GRCh38.p7	14:44936868	GTTCAAGAGCAATCA[A/G]TTCTACTAACTGATT	54813
rs190056378	snp	C/T	0.0130921	0.0798413	intron-variant	FAM179B	GRCh38.p7	14:44971286	GTGTGTTTTTACACA[C/T]TGTGTCTTTCAAGGA	54813
rs190071431	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948087	TATGAAAAAGTTAAA[A/G]TCTAGACTTAAAAGT	54813
rs190077213	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926799	AGGCGTGAGCCACTG[C/T]GCCCGTCCTAAAATC	54813
rs190116817	snp	C/T	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44971004	GTGGGGTTTTTGTTT[C/T]GTTTTGTTTTTGTTT	54813
rs190311523	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44955917	AAACTGATCATCAAT[A/C]ATAATAACTGCAATT	54813
rs190315282	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44976744	CAGCACATGATACTG[A/G]GGTTCTTATGTCTTA	54813
rs190328474	snp	G/T	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44932664	TGTTTCTGAAAGAAC[G/T]CCAGGATAGAATCCA	54813
rs190373098	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952142	TGGGATTACAGGTGT[A/G]AGCCACTGAGCATGA	54813
rs190385150	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44948021	ACACGTTCTGTTAGT[C/T]ATTCCAGTGTTGATC	54813
rs190393178	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44938395	TTTTTTTTTTGAGAC[A/T]GAGTCTCGCTCTATC	54813
rs190540058	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44929671	CTGGAGCAATATGAG[A/C]TTGATGGAAAAACAA	54813
rs190617032	snp	C/G	0.00166355	0.0287925	intron-variant	FAM179B	GRCh38.p7	14:44973241	GTTATGCTGCTGCTC[C/G]TTTTTTTTTAAATTA	54813
rs190644946	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44958955	AATCCTGTATAAAAT[A/G]AGCTCATAATTTCTT	54813
rs190733940	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44968410	GACTACAGGCACCCG[C/T]CACCATGCCCAGTAT	54813
rs190739926	snp	A/G	0.00676609	0.0577691	intron-variant	KLHL28	GRCh38.p7	14:44944900	TATTTTAGGAAGAAG[A/G]AAAAAAACTAAAAAG	54813
rs190750433	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44959935	AAAAAAAATCTGCTT[C/T]GTAATAAAAAGAATA	54813
rs190760517	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44939109	TACTTGTGCCTTCTA[A/G]AGTAGCAGCCTGAGC	54813
rs190970792	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44949479	ATATATAAGCTAGTT[C/G]AGTTAGCTAAATCAG	54813
rs190972960	snp	A/G	0.0023933	0.0345097	intron-variant	FAM179B	GRCh38.p7	14:44971836	TCTACAAGTATGTTG[A/G]GGTTTTCCATCTGTA	54813
rs191027873	snp	A/G	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960758	ACTGATATTCAAATC[A/G]TACTTTAAGGCAAAA	54813
rs191280117	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44943986	TCCCAAAGTGCTGGG[A/G]TTACAGGTATTTTGA	54813
rs191516998	snp	A/G	0.00438332	0.0466095	intron-variant	FAM179B	GRCh38.p7	14:44966262	AGATAACCTGAGGTC[A/G]GGAGTTGGAGACCAG	54813
rs191587116	snp	A/G	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44969629	TCATCACCATACCCA[A/G]GGTCATCTAGGTTTT	54813
rs191598846	snp	C/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44946878	TTGATCATTAATTCA[C/G]ATCATGCCCACTCAA	54813
rs191608962	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	KLHL28	GRCh38.p7	14:44923834	AATGTTTCTTTAGTA[A/C]ACGTCTGAATGTGTG	54813
rs191633912	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44972332	CCATGTGAATTTAAG[A/G]AGAATGTGCAGTCTG	54813
rs191638335	snp	G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44951252	GGGAAATAGAGAGGT[G/T]AGTGGAAAATTGGGA	54813
rs191639885	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928526	AAAAGTACCAAAATA[A/G]AAAGCAGCCCTTTGT	54813
rs191707081	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927722	TACTCAAGTAAACAT[C/T]GAGTTCCAGTTTTCC	54813
rs191778069	snp	G/T	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44972275	TAAAGTGTGTGTGTG[G/T]TTTTTTTTTGCGATA	54813
rs191934648	snp	C/G/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44954599	TGTGTCACCATTTAT[C/G/T]TACGATAGGGAAGAT	54813
rs191993348	snp	A/G	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44950724	AAAATAGACAAAATT[A/G]TATAAAAAGCAGTTG	54813
rs192017617	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44957988	GAAATAAAGAAGGAT[A/C]CATGGAACAATCATT	54813
rs192024049	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44979439	ATAAGGGCACTAATC[C/T]CATACTTGAGGGTGG	54813
rs192028771	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44935505	CATACACTATATAAC[A/T]TATCAATTAAGTGAA	54813
rs192123455	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44975592	CCACCTCAGCCTCCC[A/G]GATAACTGGGATTAC	54813
rs192258092	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44932498	AGAAAATTCTAGCAG[C/T]TGTTTAAGACTATGG	54813
rs192265727	snp	G/T	0.00835141	0.0640778	intron-variant	KLHL28	GRCh38.p7	14:44952031	GCCCGACTAGTTTTT[G/T]TATTTTTTTTGTAGA	54813
rs192273725	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962209	GGTGCCCTTGGTTAC[C/G]CCCGGTGGCAGCTGT	54813
rs192318751	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44935030	CATATATGTCCAAGA[A/G]TGTTTACTACAGTAT	54813
rs192502604	snp	C/T	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44977457	TAGCTGGGATGGTCT[C/T]GATCTCCTGACCTCA	54813
rs192558528	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, intron-variant	KLHL28, FAM179B	GRCh38.p7	14:44961123	ACAAAATTCTCAGTT[C/T]GCCTAAAATAAATAA	54813
rs192573672	snp	A/T	0.00795532	0.062565	intron-variant	KLHL28	GRCh38.p7	14:44940477	AAATGCTTTCAATGT[A/T]TTGCCATCCTTATGA	54813
rs192672712	snp	G/T	0.0119091	0.0762411	intron-variant	FAM179B	GRCh38.p7	14:44972910	TCATTTTGCTATAAT[G/T]TTGATGAGGAAAAAA	54813
rs192809033	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44956543	AGAAAATAGAAAAAT[C/T]ATGTTAAACAATACC	54813
rs192818338	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44942417	ACAATAACATCTTAT[C/T]TAATCAATCTGATAT	54813
rs192978872	snp	A/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44973639	CCAGGTTTTTGACCT[A/G]TATAATTTTCCTTTT	54813
rs193011817	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44957161	AATAATATGTTGTTA[C/G]GATTTGCTGCAAAAT	54813
rs193080757	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44969012	TACTTGGAGTTATAC[A/G]GTAGCTTGCATTTTC	54813
rs193195451	snp	A/C	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44952145	GATTACAGGTGTGAG[A/C]CACTGAGCATGACCA	54813
rs193206735	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44977927	AGTGCTGGGATTACA[C/G]GCATGAGCCACTGTG	54813
rs193266452	snp	A/T	0.0123036	0.0774623	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928693	CTAAAATAAAAAAAA[A/T]AAAAAAAAAAAAGCA	54813
rs199500373	snp	A/C/G	0.000197799	0.00994298	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963912	CATTTGCATCTGCTC[A/C/G]CTGCTGACCTATCCT	54813
rs199543632	snp	C/T	1.6607e-05	0.00288153	missense	KLHL28	GRCh38.p7	14:44945904	TTAAGTTAGCAAGCA[C/T]GTAGGTCGGGGATGT	54813
rs199572352	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44966939	CTCCAGCCTGCTCAA[C/G]AGTGAGACCCAGACT	54813
rs199601468	snp	G/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927997	TAAGCACAAATGAAT[G/T]AAGCCATTAAAAATG	54813
rs199638602	snp	A/G	1.64806e-05	0.00287054	missense	KLHL28	GRCh38.p7	14:44945666	GCATACTCCACAATG[A/G]CCTGGAGAGCAGTTT	54813
rs199672203	snp	C/T	0.00128501	0.0253151	missense	KLHL28	GRCh38.p7	14:44945186	AGATGTTTACAAGTG[C/T]GATCATCACGAATAA	54813
rs199813894	snp	C/T	0.000328132	0.0128046	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962460	GCTTCTGCTGCCGCC[C/T]TTTCCAGTCCTCTCT	54813
rs199846964	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44955651	ATTAGCTGGATGTGG[G/T]GGCACATGCCTGTAG	54813
rs199867476	snp	A/C/T	3.29632e-05	0.00405964	synonymous-codon	KLHL28	GRCh38.p7	14:44934312	TTCTCCTGCAAGTAC[A/C/T]ACTACTCCAAGAGTA	54813
rs199955572	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44937058	CATCTGAAGTAGGAA[A/C]AGTCTAGGACTGAGC	54813
rs199956782	snp	C/T			missense, intron-variant	KLHL28	GRCh38.p7	14:44931393	GATGAGGATCGTATC[C/T]TTCAATGCTGGACAA	54813
rs199992988	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44956002	AAGTCCTAATGGTCA[A/C]CACCGGACGATGCTA	54813
rs200020790	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44952901	AGGAAGGGTAAGTAC[A/C]ATAAAAAAAAAAAAA	54813
rs200022960	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935890	TATATATATATGTGT[A/G]TATATATATATATCT	54813
rs200143945	snp	A/G	1.67357e-05	0.00289268	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962912	TCTCGGACGTTCTCC[A/G]GGGTCAGGGGGAGGC	54813
rs200254034	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44967007	CTAGCCTTACTTTGG[-/T]TTTTTTTTTTCTTGC	54813
rs200256990	snp	A/G	0.000379084	0.0137622	missense	KLHL28	GRCh38.p7	14:44945187	GATGTTTACAAGTGC[A/G]ATCATCACGAATAAG	54813
rs200275778	snp	C/T	0.000580494	0.0170267	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928994	CATGCAGTACAAGTT[C/T]CACCACCATACTATT	54813
rs200300639	snp	C/T	4.95152e-05	0.00497545	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963774	CAACAAGTTGGTGAT[C/T]AAACAAGAATACATG	54813
rs200506515	in-del	-/T	0.00478085	0.0486577	intron-variant	FAM179B	GRCh38.p7	14:44969569	AGTCCAGTTAATCAG[-/T]TTTTTTCTTGCATGG	54813
rs200577505	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44955068	AGTAATGATATGATA[G/T]TCTATCAACCCTAGG	54813
rs200647599	snp	C/T	3.29712e-05	0.00406011	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964337	TGCACATTTATGGAT[C/T]TTACAGCCCAACTAT	54813
rs200691331	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44974843	TTCTGTCTCTTCAGA[C/T]TTTGTTTTTACCTTT	54813
rs200711290	snp	A/T	0.00159617	0.0282053	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928975	ACTGGGCCATCCGGA[A/T]GTTCATGCAGTACAA	54813
rs200711722	in-del	-/T	0.0364509	0.129988	intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937314	CCACCCTCAGCTAAC[-/T]TTTTTTGTATTTTTA	54813
rs200736260	in-del	-/TTT	0.105924	0.204309	intron-variant	KLHL28	GRCh38.p7	14:44933314	TCTTTTCTTTCTTTC[-/TTT]TTTTTTTTTTTTGAG	54813
rs200745215	snp	A/T	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44965873	TACAAATAGTAATTT[A/T]TTTTTTTTTTTTTTT	54813
rs200749226	in-del	-/TA			intron-variant	FAM179B	GRCh38.p7	14:44973592	TTCTCTCTCTCTCTC[-/TA]TCTCTATATATACAT	54813
rs200775208	snp	C/T	0.000377255	0.013729	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962800	CGGCGGGGCGGTCGA[C/T]TTGGCTTCCCCCGAC	54813
rs200836370	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44967290	TTTGAATCTCCCTTC[A/G]TTCACAATAAAATCC	54813
rs200840473	in-del	-/A			intron-variant	KLHL28	GRCh38.p7	14:44951903	CCTGTTGCCCTGGCC[-/A]GGGTGTGGTGGCGAG	54813
rs200986079	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44935900	TGTGTGTATATATAT[A/C]TATCTTTACCCTCCC	54813
rs201049020	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44964975	AAAAAAAAAAAAAAG[A/G]AAAAAGAAAAAGCCT	54813
rs201064517	in-del	-/TTTC			intron-variant	KLHL28	GRCh38.p7	14:44933302	GATACAATCTTTTCT[-/TTTC]TTTCTTTCTTTTTTT	54813
rs201088194	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44958701	CTTGCTTTCTTCTGT[A/G]TTATTTCTGAATCCA	54813
rs201109759	snp	C/T	4.94564e-05	0.0049725	synonymous-codon	KLHL28	GRCh38.p7	14:44945218	ATGATTTGCTTCATA[C/T]AGTCTAGTGAGAAAC	54813
rs201170442	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44969162	TTTCTTTCTTTCTTT[C/T]CTTTCTTTTCTTTTT	54813
rs201192602	in-del	-/TA			intron-variant	FAM179B	GRCh38.p7	14:44973594	CTCTCTCTCTCTCTC[-/TA]TCTATATATACATAT	54813
rs201212449	in-del	-/ATA			intron-variant	FAM179B	GRCh38.p7	14:44979192	ATAATAATAATAATA[-/ATA]CTGTTTTCAAAGGCA	54813
rs201237706	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44973549	ATAAGTTTTTTTTTT[A/T]ACCTTTACTTATTCT	54813
rs201256909	snp	A/T	0.475259	0.108435	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928684	GAAGGAGAGCTAAAA[A/T]AAAAAAAAAAAAAAA	54813
rs201299653	in-del	-/A			intron-variant	FAM179B	GRCh38.p7	14:44976635	TCAACCTTTACCTTT[-/A]AAAAAAAAACTCTTA	54813
rs201338324	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44943610	TGCAGTGAGCTGAGA[G/T]TGCACCACTGCACTC	54813
rs201359279	in-del	-/C	0.0130921	0.0798413	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928803	TTGGCAAAGTCTTTA[-/C]TTTTTTTTTTTCTCT	54813
rs201382313	snp	C/T	1.65105e-05	0.00287315	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963459	TTCCAACAGCAATCT[C/T]AAATTTGGGATTATT	54813
rs201483298	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44940729	ATTCACAACTTTCTA[A/T]CATTGCTTTTGATAT	54813
rs201531124	snp	C/T	3.30093e-05	0.00406246	missense	KLHL28	GRCh38.p7	14:44945859	GAAGAAGATTCAAGC[C/T]CTGCAGAAGTTGTTC	54813
rs201587443	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44969163	TTCTTTCTTTCTTTT[C/T]TTTCTTTTCTTTTTT	54813
rs201609162	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44931556	ACTGCAAATATTTAA[A/G]AAAAATTTAATTTAC	54813
rs201633630	in-del	-/TTT	0.0115144	0.0749975	intron-variant	FAM179B	GRCh38.p7	14:44966612	TTTTTTGTTACTAAA[-/TTT]TTTTTAACTTTTTCA	54813
rs201652524	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44977631	AAAGGTGTTAAATGT[A/G]TGACATGCTTTAGAC	54813
rs201731863	in-del	-/G			intron-variant	KLHL28	GRCh38.p7	14:44932250	GAGGAAGAGAGGGGT[-/G]GGGGGGTGGGGAGAA	54813
rs201775520	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44974795	AAGTTAATACAACAT[C/T]CCTGCCATATCTGAT	54813
rs201824274	snp	A/G	0.000757975	0.0194528	synonymous-codon	KLHL28	GRCh38.p7	14:44945170	TAGGGCTTCATTCAA[A/G]AGATGTTTACAAGTG	54813
rs201830785	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44969145	CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT	54813
rs201842534	snp	C/T	0.000220795	0.0105047	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962453	CCGCGCTGCTTCTGC[C/T]GCCGCCCTTTCCAGT	54813
rs201855402	in-del	-/A			intron-variant	FAM179B	GRCh38.p7	14:44979032	ATAGAAATAACAGAT[-/A]AAAAAAAAAGGTTAG	54813
rs201893106	snp	G/T	1.64844e-05	0.00287087	synonymous-codon	KLHL28	GRCh38.p7	14:44945811	TAACATCACCTACTC[G/T]AAGAATGATGTCACA	54813
rs201928552	snp	A/C	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44952913	TACCATAAAAAAAAA[A/C]AAAACAAACACAGGA	54813
rs201945385	snp	A/G	1.65097e-05	0.00287308	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963344	TGAGGAGACACTACA[A/G]TCGCCGCCTGGAGTC	54813
rs202124310	snp	A/C			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960719	TTCCCCACCCCCACC[A/C]CCCCAAAAACAAAAC	54813
rs202173126	snp	A/G	0.000115328	0.0075928	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964131	GATGAATGCTGTGCA[A/G]GCCAGATTGGCTAGG	54813
rs202187853	snp	G/T	1.6489e-05	0.00287128	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963425	TTCCTGAAGATCCCC[G/T]TCCCTGTGCAGTGAC	54813
rs367584301	snp	A/G	8.82324e-05	0.00664142	intron-variant	KLHL28	GRCh38.p7	14:44944990	TTTAAAAAGCATAAA[A/G]TCAATTAGCATCATT	54813
rs367613115	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44950708	TTTTCTCATTTGTAA[A/G]AAAATAGACAAAATT	54813
rs367642428	snp	A/G	3.30087e-05	0.00406242	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963730	TTCTTGGGACCAGTT[A/G]TAGCAGCTTCTGTCA	54813
rs367701769	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44967804	GAGGAGGTGAATTGA[C/G]TGTTCTCTATGGTTC	54813
rs367703243	snp	C/T	0.000132042	0.00812424	synonymous-codon	KLHL28	GRCh38.p7	14:44934171	CATTCCATCCAATAC[C/T]GCTGCAGCAAAACAA	54813
rs367710275	snp	G/T	1.65556e-05	0.00287707	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962674	AGCAGCTGGTCTGAG[G/T]CTGGAGGCGGTTTGT	54813
rs367715479	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926728	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	54813
rs367734635	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962284	CCCGGAGTTGGGGGC[A/G]GCCTGGCGGCAGGCT	54813
rs367886681	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935870	TATGTATGTGTATGT[A/G]TATGTATATATATAT	54813
rs367943711	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44969499	CACTTTGTGTCTTGT[C/T]TTCTCATTCTCTTGA	54813
rs367945427	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935886	TATGTATATATATAT[A/G]TGTGTATATATATAT	54813
rs367948234	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44939737	GCCCACTTAAGTTAT[C/T]TCTAAAAAGTTCCAG	54813
rs368091743	in-del	-/CTTT/TTT			intron-variant	FAM179B	GRCh38.p7	14:44969145	TTCCTTCCTTCCTTC[-/CTTT/TTT]CTTTCTTTCTTTCTT	54813
rs368193077	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44974413	TTCTTACATGTTGTC[A/T]TTTTTCATTATAGCC	54813
rs368253610	snp	A/G	0.000413938	0.0143805	intron-variant	FAM179B	GRCh38.p7	14:44964494	TAATTTTCTTGAGTC[A/G]AAAGTGTGAAGAATT	54813
rs368278098	snp	A/C	0.00199481	0.0315187	intron-variant	FAM179B	GRCh38.p7	14:44973598	TCTCTCTCTCTCTCT[A/C]TATATACATATATAT	54813
rs368286174	snp	C/T	1.69645e-05	0.00291238	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962508	CCGCAGTCGTCCTTC[C/T]GCCCCAGAGACCGAT	54813
rs368301682	snp	G/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926438	TATACACTAATTTGA[G/T]AGTGGAGATGATACA	54813
rs368448387	snp	A/C	0.000153988	0.00877328	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963523	GAAGACTATAAGAAC[A/C]GGACCCAGGCCGTCG	54813
rs368515894	snp	G/T	3.29603e-05	0.00405944	missense	KLHL28	GRCh38.p7	14:44945680	GGCCTGGAGAGCAGT[G/T]TCATCAATGCATTGA	54813
rs368535199	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935862	TTTGCATGTATGTAT[A/G]TGTATGTGTATGTAT	54813
rs368626661	snp	A/G	0.00119737	0.0244387	intron-variant	KLHL28	GRCh38.p7	14:44942369	CTAATTTAGGATCTC[A/G]TCATCTCTTGCCTAT	54813
rs368628822	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44968946	CCAAGCCTTAGCAAC[C/G]AGTGGTCTTTTTTTC	54813
rs368691671	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44936428	AATAAGTAGAGAGGT[A/G]GAAGGGTTGGTCTTA	54813
rs368703220	snp	C/T	0.000148438	0.00861376	missense, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929099	GCCACGTATCTGAGA[C/T]AGGATCATATTTCTG	54813
rs368769577	snp	C/T	0.000207314	0.0101791	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962403	GTTTCTTCCAACCAC[C/T]ACCACCTGACAACCC	54813
rs368877584	snp	A/G	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44929267	ACTAAAAATAAATTT[A/G]TATTTTAATGTTTTA	54813
rs368888947	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940197	AACCTACTCTCACAA[C/T]AATAGCATTAATCCC	54813
rs368953046	snp	C/T	8.24069e-05	0.00641846	synonymous-codon	KLHL28	GRCh38.p7	14:44934270	TTGTAAATAAGATTG[C/T]CCATCATAACCACCT	54813
rs368957396	snp	A/G	1.65198e-05	0.00287395	synonymous-codon, intron-variant	KLHL28	GRCh38.p7	14:44931403	GTATCTTTCAATGCT[A/G]GACAAATGTGAGACT	54813
rs369064596	in-del	-/A	0.00159617	0.0282053	intron-variant	KLHL28	GRCh38.p7	14:44930294	GTGCTCCAACATTTG[-/A]AACTTTTTTTTTTGA	54813
rs369093799	snp	A/C	0.0898077	0.191933	intron-variant	FAM179B	GRCh38.p7	14:44973590	ACTTTCTCTCTCTCT[A/C]TCTCTCTATATATAC	54813
rs369133730	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44942667	CTGAATATCCCATAA[C/T]GTATCATGCCATTGT	54813
rs369189995	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44976940	TTCTAAACCTAAAAA[C/T]TAGTATTTTAAAAAT	54813
rs369302120	in-del	-/TTCC			intron-variant	FAM179B	GRCh38.p7	14:44969111	CATTTCTTTCTTTCT[-/TTCC]TTCCTTCCTTCCTTC	54813
rs369328184	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44950476	AATTCAAAACTGGTA[C/T]ACCATCAACATATGA	54813
rs369381342	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44972274	TAAAGTGTGTGTGTG[-/T]TTTTTTTTTTGCGAT	54813
rs369443776	snp	A/G			downstream-variant-500B	KLHL28	GRCh38.p7	14:44924255	CCTATCTATGCATAA[A/G]ACCCTAAGAGCTGAG	54813
rs369447680	snp	A/G	1.69735e-05	0.00291315	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962762	CTTCTGAGGCCTTCC[A/G]GGCTTTGCAAGCTGC	54813
rs369464790	snp	A/G	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44975298	AAATACTGAGTTGAA[A/G]CAAGTTTTATTTTCT	54813
rs369468853	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44944046	TTGCCATTGATGAAA[C/T]GTCAAGTTTCCTAAC	54813
rs369513465	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44964981	AAAAAAAAGGAAAAA[A/G]AAAAAGCCTCCACAG	54813
rs369516711	in-del	-/CT			intron-variant	FAM179B	GRCh38.p7	14:44970770	AGATTTTGTCTAATG[-/CT]TTTTTGCATCTATTG	54813
rs369547613	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44965528	TATGTTTACTTGATT[A/C]GATTCAAAATAAATA	54813
rs369559749	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44928010	ATCAAGCCATTAAAA[A/G]TGCAAAAGACTATCA	54813
rs369599313	snp	A/G	1.64893e-05	0.0028713	missense	KLHL28	GRCh38.p7	14:44934181	AATACCGCTGCAGCA[A/G]AACAACTTCTTGTTG	54813
rs369605488	in-del	-/TC			intron-variant	FAM179B	GRCh38.p7	14:44973579	TCCTCCAGTGTACTT[-/TC]TCTCTCTCTCTCTCT	54813
rs369605562	snp	A/G	1.69404e-05	0.00291031	synonymous-codon	KLHL28	GRCh38.p7	14:44945032	GCCTTCTATTTACCT[A/G]TCCAAACAGGCAAAG	54813
rs369781277	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44941906	CAATCAATCCTTTTT[C/T]CTCTCTATATTTTCT	54813
rs369821527	snp	C/T	1.64738e-05	0.00286995	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963071	GAGAGGTGCTGAGAA[C/T]GCTTATACAACAAGG	54813
rs369875588	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44939249	TTCCCCCAAACCATT[A/C]TGCCCTCCTAGTGTT	54813
rs369926539	snp	G/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44924494	AATAAAATAAAACCC[G/T]GATGCTAAAAAGGTA	54813
rs369978272	snp	C/T	0.000230745	0.0107387	missense	KLHL28	GRCh38.p7	14:44945444	ACAGCTTCAAAATTC[C/T]GGCATATGTATTTAG	54813
rs370003032	snp	C/T	0.00422617	0.0457736	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962409	TCCAACCACCACCAC[C/T]TGACAACCCTGCATG	54813
rs370050539	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44939190	GAGAGCAGACTCCCA[A/G]GGTGGCCATGGGCAG	54813
rs370052421	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44972779	TTAAAATGGGTTTCT[C/T]GTAGACAGCCTATAT	54813
rs370176029	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44957995	AGAAGGATCCATGGA[A/G]CAATCATTGCCTTCC	54813
rs370204109	snp	G/T	1.64904e-05	0.00287139	synonymous-codon	KLHL28	GRCh38.p7	14:44945551	TTGGCTTTCAAGAAA[G/T]GCACAACATTCTTTC	54813
rs370409190	in-del	-/CT			intron-variant	KLHL28	GRCh38.p7	14:44958732	TGTTATGACAGGCGT[-/CT]AAGTTACATAATTAA	54813
rs370424922	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44927993	TTAATAAGCACAAAT[A/G]AATCAAGCCATTAAA	54813
rs370437319	snp	A/T	3.29522e-05	0.00405894	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963195	CACCGAGGTGATAAT[A/T]TCCCTAGCCCGAAAG	54813
rs370595434	snp	A/T	0.0236746	0.106192	intron-variant	KLHL28	GRCh38.p7	14:44947828	GGTAACAGCCTCCAC[A/T]GCTGATCTCTGCAAA	54813
rs370658518	snp	C/T	1.65272e-05	0.0028746	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963689	TGCATTTACTGGTTA[C/T]TCGCCTTGGAGAGCA	54813
rs370664242	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44930973	ATTACTGATATACAA[C/T]AGAAAACAAAACAGA	54813
rs370676288	snp	A/C	1.65562e-05	0.00287712	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963533	AGAACCGGACCCAGG[A/C]CGTCGAAGAACTAAA	54813
rs370701358	in-del	-/TATATATATG			intron-variant	KLHL28	GRCh38.p7	14:44935860	TTTTGCATGTATGTA[-/TATATATATG]TGTGTATGTGTATGT	54813
rs370752491	snp	C/G/T	9.89392e-05	0.00703288	synonymous-codon, utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929088	AGCTGAATCCAGCCA[C/G/T]GTATCTGAGATAGGA	54813
rs370813418	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44952688	ACAGGTGTCCACCAC[C/T]GCGTTTGGCTCAAAA	54813
rs370830927	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44948182	CCTCGTTAACTTTAC[C/T]TTCTCAATCTTTGTT	54813
rs370889023	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44967904	ATTTCCTTGTATTAT[A/C]AGCATTATCTGGTAG	54813
rs370966232	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44953192	AAGGTGGAATCTCTG[A/C]GAGGGAAAAGAGAAA	54813
rs370980257	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44967390	TTGCTAGACCAGCAA[A/C]AGCAACCAACTACCT	54813
rs371013737	snp	A/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926139	GAAACTTCTCACAAA[A/T]TTGTAAAAGAAGGCG	54813
rs371072899	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44945002	AAAATCAATTAGCAT[C/T]ATTCATTTAGGAAAG	54813
rs371132624	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935864	TGCATGTATGTATGT[A/G]TATGTGTATGTATAT	54813
rs371162313	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44938410	TGAGTCTCGCTCTAT[C/T]GCCCAGGCTGGAGTG	54813
rs371224925	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44950067	AAAAAAGGAGGTCTG[A/G]GTTATCACATGAAAA	54813
rs371237149	snp	A/G			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926800	GGCGTGAGCCACTGC[A/G]CCCGTCCTAAAATCA	54813
rs371253230	snp	A/G	1.64958e-05	0.00287187	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964351	TCTTACAGCCCAACT[A/G]TCTGTACCCGAAGGG	54813
rs371257241	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44936969	GCTGGCAAGAAAAAA[A/C]CACTGTCAAAGAGTG	54813
rs371275878	snp	C/G	1.6631e-05	0.00288362	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962711	GAGATGAAGAGGACA[C/G]TCGGCTCCTTCAACT	54813
rs371304433	in-del	-/A	0.0115144	0.0749975	intron-variant	KLHL28	GRCh38.p7	14:44950873	CTTTCCATGCATACC[-/A]AAAAAAGGAAGGAAG	54813
rs371334535	snp	A/T			intron-variant	FAM179B	GRCh38.p7	14:44973284	AGTTTCCCTAGAGTG[A/T]GTAATACACATTTAC	54813
rs371438184	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44980026	AAAATCTAGACTATG[A/G]ATAACCTTATTTAGT	54813
rs371633827	snp	G/T	0.000430072	0.0146578	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963675	CACACTTGAAGTCCT[G/T]CATTTACTGGTTATT	54813
rs371718117	snp	A/C			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960716	CTATTCCCCACCCCC[A/C]CCCCCCCAAAAACAA	54813
rs371729621	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935872	TGTATGTGTATGTGT[A/G]TGTATATATATATGT	54813
rs371905593	in-del	-/GTTTT			intron-variant	FAM179B	GRCh38.p7	14:44973918	GTTCTGTTTTGTTTT[-/GTTTT]TCCTTTATCTTCTTT	54813
rs371907788	snp	C/T	0.000798403	0.0199641	intron-variant	KLHL28	GRCh38.p7	14:44934917	AAATATACACAAATG[C/T]TCACAGAAGCACAAC	54813
rs371933146	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935888	TGTATATATATATGT[A/G]TGTATATATATATAT	54813
rs372175514	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44954748	GATATTTTTGAATAT[A/G]CTCTGTTTTATAGAT	54813
rs372220648	snp	G/T	1.69479e-05	0.00291095	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962509	CGCAGTCGTCCTTCC[G/T]CCCCAGAGACCGATG	54813
rs372238331	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44969194	TTTTTTTGTGAGACA[G/T]CCCAGGCTGGAGTGC	54813
rs372264898	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44974758	TGCCTTTACCCCTTT[C/T]GGTGTGTGTGTCTGG	54813
rs372267594	in-del	-/G	0.00318978	0.0398085	intron-variant	KLHL28	GRCh38.p7	14:44953451	AGAGTCCTTATGAAC[-/G]GATTGATCCACTTAT	54813
rs372284840	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44968650	GAACAACCTGACCCA[C/T]CTCATCCGGTACTTT	54813
rs372295563	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44941935	CTCACCAGGCAAAAG[A/G]AGGAACATTTAAACT	54813
rs372329829	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44957190	ATAATAGGGGATGAG[A/G]TTGTGGAAGGGGATA	54813
rs372431128	in-del	-/AACAA			intron-variant, upstream-variant-2KB	KLHL28, FAM179B	GRCh38.p7	14:44960731	CCCCCCCAAAAACAA[-/AACAA]AACAAAACAAAACTG	54813
rs372467308	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44953447	TGGCAGAGTCCTTAT[A/G]AACGGATTGATCCAC	54813
rs372508081	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44940449	ATTTAACATATTTGC[A/G]CAACTATTCAAAAAA	54813
rs372510539	snp	C/T	0.000153988	0.00877328	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963327	TCGTCTGCCCTCTGC[C/T]CTGAGGAGACACTAC	54813
rs372740537	snp	C/T	7.53651e-05	0.00613815	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962406	TCTTCCAACCACCAC[C/T]ACCTGACAACCCTGC	54813
rs372774861	snp	A/G	1.64749e-05	0.00287005	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964042	GTATTGGCATCATCA[A/G]TGGGCTCAGGTAAAA	54813
rs372774955	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44964598	TGATTTTAAATCCAT[C/G]TGAATGTTGGTACTC	54813
rs372839378	in-del	-/T			intron-variant	KLHL28	GRCh38.p7	14:44932257	GAGAGGGGTGGGGGG[-/T]GGGGAGAAAAACCTT	54813
rs372863808	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44965785	ACCCTAAGAATACCC[C/T]GACAACTTTTCACCC	54813
rs372973352	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44973592	TTTCTCTCTCTCTCT[A/C]TCTCTATATATACAT	54813
rs372985268	snp	C/G			intron-variant	FAM179B	GRCh38.p7	14:44964814	TCTGGGAATGAAGAT[C/G]AGGCCAGTTTCACAC	54813
rs373067345	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44929812	AGCCTAGGACCCTGT[C/T]TAGACACTGAAATAA	54813
rs373247606	snp	A/G			intron-variant, downstream-variant-500B	KLHL28	GRCh38.p7	14:44937532	TCTCAGTGATAGTAA[A/G]ACTAAAGGTTATGAT	54813
rs373351034	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44952242	CACAGAATTCTAACA[C/T]TTTCAAATATAGAGT	54813
rs373351897	snp	C/T	0.00398564	0.0444627	intron-variant	KLHL28	GRCh38.p7	14:44940799	AAGCATTCATCTATC[C/T]TATATCTTTACCCTA	54813
rs373397029	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44972215	TCACCATCTTAATTT[G/T]GCCTGAGAGCAAATA	54813
rs373487359	snp	A/G/T	4.94208e-05	0.00497075	upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44963115	GATGCCCGACTTAGA[A/G/T]CTTCCACAGCACTAC	54813
rs373580836	snp	A/G	3.29527e-05	0.00405898	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964213	ATGCCATCTTCTGCC[A/G]GGGGTAGGTCAAACC	54813
rs373660498	in-del	-/TCTCTC			intron-variant	FAM179B	GRCh38.p7	14:44973579	TCCTCCAGTGTACTT[-/TCTCTC]TCTCTCTCTCTCTAT	54813
rs373736878	snp	A/C			intron-variant	KLHL28	GRCh38.p7	14:44940438	GTCCATTCAACATTT[A/C]ACATATTTGCACAAC	54813
rs373807743	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44955087	ATCAACCCTAGGGTC[A/T]CTGTGATCTAGGATT	54813
rs373853153	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44968495	CCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA	54813
rs373864283	snp	A/G	0.00119737	0.0244387	intron-variant	FAM179B	GRCh38.p7	14:44980095	ATAGCAGGTCTCAGT[A/G]CTTCCTTTTATGTAT	54813
rs373892418	snp	A/G	0.000153988	0.00877328	intron-variant	KLHL28	GRCh38.p7	14:44945949	GAAAAATAAAAAAGC[A/G]TAGACAGTTATTTCA	54813
rs373899846	snp	C/T	0.000214244	0.0103478	missense	KLHL28	GRCh38.p7	14:44945763	TGAAATACGGGCTGA[C/T]GCTGGCAAGTACCAC	54813
rs373914269	snp	A/C			intron-variant	FAM179B	GRCh38.p7	14:44975834	TTTCAAGTGACTCAA[A/C]ACAACACAGCTTTGG	54813
rs373919731	snp	C/T	0.000115423	0.00759593	synonymous-codon	KLHL28	GRCh38.p7	14:44945536	ATTACCAGGATCAAG[C/T]TGGCTTTCAAGAAAT	54813
rs373940153	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44967253	TACTGCAGGGTTCTT[-/T]CTCATCTTCCTTTAT	54813
rs373959079	snp	C/T	0.00716266	0.059414	intron-variant	KLHL28	GRCh38.p7	14:44930419	ACAGGCATGTGCCAC[C/T]GCACCAGGCTAATTT	54813
rs373999644	snp	C/T	0.000115391	0.00759487	synonymous-codon	KLHL28	GRCh38.p7	14:44934198	ACAACTTCTTGTTGT[C/T]GTCATTGGTGCCACA	54813
rs374030406	snp	C/G	1.64803e-05	0.00287052	missense	KLHL28	GRCh38.p7	14:44945121	TCAAGACTGTCTGAT[C/G]AGAGAGTCTATGTTC	54813
rs374034646	snp	A/G			upstream-variant-2KB, missense, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962773	TTCCAGGCTTTGCAA[A/G]CTGCTTTGCCGCGGC	54813
rs374089650	snp	C/T	4.94491e-05	0.00497213	missense	KLHL28	GRCh38.p7	14:44934359	TTCTCTCTAGAGAAG[C/T]CCAAGTATTTGTATC	54813
rs374139384	in-del	-/CA			intron-variant	FAM179B	GRCh38.p7	14:44966938	CTCCAGCCTGCTCAA[-/CA]GAGTGAGACCCAGAC	54813
rs374195633	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964359	CCCAACTATCTGTAC[C/T]CGAAGGGTATTAAGT	54813
rs374206902	snp	C/G	1.80328e-05	0.00300268	intron-variant	KLHL28	GRCh38.p7	14:44945972	TTATTTCAAAGTAAA[C/G]TTGTCAAAAACACTG	54813
rs374210841	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44938001	TACATTTCCAACATA[C/T]GAACTTTTGGGGAAC	54813
rs374434772	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44967474	CACAGTCAGAATTTT[G/T]TGGTCAAACTTTTCT	54813
rs374462678	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44958379	AAATGGTGAACAGAA[A/G]TCAAGATTACTCTTA	54813
rs374501917	snp	A/G	8.25294e-05	0.00642323	missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963455	CTCTTTCCAACAGCA[A/G]TCTTAAATTTGGGAT	54813
rs374516713	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	KLHL28, FAM179B	GRCh38.p7	14:44961752	TCTTTCCACCTGCTC[C/T]GCTCAGTCCTTTGCC	54813
rs374658913	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44954185	TCATTGCTGTGGGAA[C/T]AGAAAATGATACAAA	54813
rs374837394	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44972879	AAGTCCTCAAATAAC[A/G]TTATTTTGTTCAACA	54813
rs374841750	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44939284	GACTACAACGGGAGG[C/T]ACAGCCTCAAAGATC	54813
rs374842710	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44943183	GCAACTGCTCAAAAA[C/T]TTTTACACTATAAAT	54813
rs374851681	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44971090	AATGAGTCAGAAAGT[A/G]TTCTCCCTGCTTCTA	54813
rs374895686	snp	G/T			intron-variant	FAM179B	GRCh38.p7	14:44965101	ATACTTCATCTATAT[G/T]TACCAGTTGTAACAT	54813
rs374904076	in-del	-/AAG	0.00279162	0.0372561	intron-variant	FAM179B	GRCh38.p7	14:44978826	AAAAGAGAAAAAAAA[-/AAG]AAGAAGAAGATCAAG	54813
rs374977399	snp	A/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44950158	TGAGGATTAAACGAG[A/T]TTATACATAAAAAGG	54813
rs375105988	in-del	-/T			intron-variant	FAM179B	GRCh38.p7	14:44969761	GATTCATTTTTTTTT[-/T]ACATGTGCATGTTCA	54813
rs375128007	snp	C/G	7.64867e-05	0.00618365	intron-variant	KLHL28	GRCh38.p7	14:44934596	ATAAAATTTAAAAAC[C/G]AAAGTGGCCCATAAA	54813
rs375211439	in-del	-/T/TTCA			intron-variant	FAM179B	GRCh38.p7	14:44969142	TCCTTCCTTCCTTCC[-/T/TTCA]TTCCTTTCTTTCTTT	54813
rs375227759	snp	C/T	1.68323e-05	0.00290101	upstream-variant-2KB, synonymous-codon, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962520	TTCCGCCCCAGAGAC[C/T]GATGATAGTCGAGTT	54813
rs375237090	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44941793	CTTGACACACAAATT[C/T]CTTGGCTTTTATGAC	54813
rs375247315	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44952940	AGGAAAGAACAGGGA[A/G]TAAAAGCATTAATTT	54813
rs375251583	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44975237	GAATGAATGAACTCA[A/G]TGGATGCCCCCCCAC	54813
rs375267232	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44951012	GATTTAGATAGTTTA[C/T]TACTTACAGATTGAA	54813
rs375331056	snp	C/T	0.00318978	0.0398085	intron-variant	KLHL28	GRCh38.p7	14:44947230	CTAAAGAGGCAGAGA[C/T]TAGAGTGCTGCAGCC	54813
rs375357874	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935874	TATGTGTATGTGTAT[A/G]TATATATATATGTGT	54813
rs375389038	snp	C/G	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44969325	CCCGGCTAATTTTTT[C/G]TATTTTTAGTAGAGA	54813
rs375413955	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44949936	CAGTCCATATCTGTA[C/G]TACAGATTTTGGGTA	54813
rs375491717	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44935868	TGTATGTATGTGTAT[A/G]TGTATGTATATATAT	54813
rs375507984	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44957631	TGTACCAGTTAACAG[G/T]CTAAGCTTTTAACAT	54813
rs375542518	snp	A/G	0.0138799	0.0821421	intron-variant	KLHL28	GRCh38.p7	14:44935852	TATATAATCTTTTGC[A/G]TGTATGTATGTGTAT	54813
rs375544551	snp	A/C	4.94401e-05	0.00497168	missense	KLHL28	GRCh38.p7	14:44945676	CAATGGCCTGGAGAG[A/C]AGTTTCATCAATGCA	54813
rs375593780	snp	A/G	6.65152e-05	0.00576655	intron-variant	KLHL28	GRCh38.p7	14:44931294	ATCATTATAGAAAAC[A/G]TTGCCTTACATGTTT	54813
rs375627770	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44939811	CCTTAACATTCTATT[C/T]ACGGCAATCTAGGCT	54813
rs375753663	snp	A/C	8.25117e-05	0.00642254	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929023	TTTCCGAGAGTTCAC[A/C]TTTGTCAAAGTGCAG	54813
rs375777657	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44947939	TCTTCCAGTAGGTAC[G/T]TTTTTTCCAGAACAT	54813
rs375782448	snp	C/T	3.29495e-05	0.00405877	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964043	TATTGGCATCATCAA[C/T]GGGCTCAGGTAAAAC	54813
rs375796593	snp	C/T			utr-variant-3-prime	KLHL28	GRCh38.p7	14:44926371	AAGATGAAATTTAGA[C/T]TTTTCAAAAACAATG	54813
rs375803829	snp	C/G/T	0.00619032	0.0552895	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962395	CGGCAATGGTTTCTT[C/G/T]CAACCACCACCACCT	54813
rs375854883	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44950214	TAGGCTCTTAATAAA[C/T]ATGAGTTATTACTAG	54813
rs375972960	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44973760	CTTCACTTGTGAAAG[A/G]TTATTTCCCAGGGTA	54813
rs375974166	snp	A/G	0.00159617	0.0282053	intron-variant	FAM179B	GRCh38.p7	14:44969381	TGGTCTTGAACTCCC[A/G]GACTCAAGCGATTGC	54813
rs376104517	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44953869	ATAGGTAAAACTGAT[C/T]ACATTTTAAAAACTT	54813
rs376183725	snp	C/T	0.000412041	0.0143475	missense	KLHL28	GRCh38.p7	14:44945261	AATGGTAATCGTACA[C/T]TGTTTAGTAACTGTG	54813
rs376315448	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44940830	TCCCTCTTTACTTAT[C/T]TCTTTATTCATCTAA	54813
rs376348966	snp	A/G/T	6.5931e-05	0.00574125	missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964283	GTAACAGAACTCAGA[A/G/T]TGCACACTGTCACTG	54813
rs376358743	snp	A/C/G	0.00139941	0.0264152	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963165	TACTGAGGACTTGTT[A/C/G]CTTGGTCTGGATCTC	54813
rs376455956	snp	C/T			intron-variant	FAM179B	GRCh38.p7	14:44970481	TGCAGACAATCATGT[C/T]ATCTGTGAACAAAGA	54813
rs376482088	snp	A/G	1.64993e-05	0.00287218	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM179B, KLHL28	GRCh38.p7	14:44963363	CCGCCTGGAGTCCCA[A/G]TTTGGAAGTCAGGTT	54813
rs376557285	snp	G/T			intron-variant	KLHL28	GRCh38.p7	14:44932254	GAAGAGAGGGGTGGG[G/T]GGTGGGGAGAAAAAC	54813
rs376560995	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44957646	TCTAAGCTTTTAACA[C/T]GTATTAATTCCTTTC	54813
rs376584185	snp	A/G			intron-variant	FAM179B	GRCh38.p7	14:44972014	TGGCCGGAGAAGGAG[A/G]AAGAGAGGGCAGGAG	54813
rs376680146	snp	C/T	0.188316	0.242271	intron-variant	FAM179B	GRCh38.p7	14:44969176	TTCTTTCTTTTCTTT[C/T]TTTTTTTTTGTGAGA	54813
rs376690431	snp	A/G			intron-variant	KLHL28	GRCh38.p7	14:44958412	AAAAAAATTCAAACC[A/G]ACAGTTTTCTTTAAA	54813
rs376701707	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL28	GRCh38.p7	14:44936305	GTGTTTGCATGCTGA[C/T]GGTAATGATACATAT	54813
rs376743692	in-del	-/GTTTT			intron-variant	FAM179B	GRCh38.p7	14:44971010	TTTTTGTTTTGTTTT[-/GTTTT]TGTTTTTTTTCTTAT	54813
rs376764484	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44934994	GTCTGAGCAACTCTA[C/T]TGATGAAAAAGGCAT	54813
rs376767391	in-del	-/G			intron-variant	FAM179B	GRCh38.p7	14:44972275	AAAGTGTGTGTGTGT[-/G]TTTTTTTTTGCGATA	54813
rs376767428	snp	C/G			intron-variant	KLHL28	GRCh38.p7	14:44953189	ATAAAGGTGGAATCT[C/G]TGCGAGGGAAAAGAG	54813
rs376852614	snp	C/T	4.96151e-05	0.00498047	utr-variant-3-prime	KLHL28	GRCh38.p7	14:44929012	CCACCATACTATTTC[C/T]GAGAGTTCACATTTG	54813
rs376857549	snp	C/G	6.88516e-05	0.00586694	missense	KLHL28	GRCh38.p7	14:44934529	GCCAAACCAATCCAA[C/G]AGTCATTCTGAGGAA	54813
rs376888974	snp	C/T	0.000399281	0.0141238	intron-variant	FAM179B	GRCh38.p7	14:44976349	CCTTTTTCCAGATAA[C/T]ATCTAATCCTTTGTT	54813
rs376951460	in-del	-/TTCTA	0.00478085	0.0486577	intron-variant	KLHL28	GRCh38.p7	14:44929480	ATATTGTTACAATTG[-/TTCTA]TTCTATTATTGTTGT	54813
rs377049122	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962342	CTTGGGGCTTGGAGA[A/G]GATCTGGAAGTCTGG	54813
rs377100144	in-del	-/G			intron-variant	FAM179B	GRCh38.p7	14:44979916	TAAGGCATGATACAA[-/G]AGTGTGCTTAGTATG	54813
rs377126553	snp	C/T			intron-variant	KLHL28	GRCh38.p7	14:44960093	ATCAAAGAGACAAAA[C/T]GTAACAGATAAAAAA	54813
rs377147509	snp	A/T	1.87855e-05	0.0030647	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	KLHL28, FAM179B	GRCh38.p7	14:44962419	ACCACCTGACAACCC[A/T]GCATGGCGGCTGCCC	54813
rs377324309	in-del	-/TCTCTCTCTC			intron-variant	FAM179B	GRCh38.p7	14:44973579	TCCTCCAGTGTACTT[-/TCTCTCTCTC]TCTCTCTCTATATAT	54813
rs377334568	snp	A/C	0.000153988	0.00877327	intron-variant	FAM179B	GRCh38.p7	14:44964506	GTCGAAAGTGTGAAG[A/C]ATTTAAATGAAAATA	54813
rs377357016	snp	C/T	0.000110702	0.00743899	intron-variant	KLHL28	GRCh38.p7	14:44931295	TCATTATAGAAAACA[C/T]TGCCTTACATGTTTA	54813
rs377361155	snp	A/G			missense, nc-transcript-variant	FAM179B	GRCh38.p7	14:44964357	AGCCCAACTATCTGT[A/G]CCCGAAGGGTATTAA	54813
rs377365388	snp	A/T			intron-variant	KLHL28	GRCh38.p7	14:44952608	GCATGATCATGGCAC[A/T]ATGCAACCTCAAACT	54813
rs377391105	snp	G/T	0.000368737	0.0135732	intron-variant	KLHL28	GRCh38.p7	14:44931590	TCTTTTGTGTCATTC[G/T]TCCTGTCAAAGCAAA	54813
rs377404771	snp	C/T	0.000798403	0.0199641	intron-variant	FAM179B	GRCh38.p7	14:44965796	ACCCCGACAACTTTT[C/T]ACCCACTGTGTTTAG	54813

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