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

ANKRD13A

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3428	snp	C/T	0.0182019	0.0936463	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038741	GATTTTCTCAGGCCT[C/T]TTTTGGATACCTTTA	88455
rs15865	snp	C/T			synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110027709	CCCCTCTGTAGCAGA[C/T]AGGAACCCGCTGGAA	88455
rs741374	snp	A/G	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110024575	ACTGGATCAACAATC[A/G]TCTCCACTATTACAA	88455
rs1044994	snp	A/T	0.350982	0.228698	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038790	TCAAACCCTCTTGTA[A/T]ATAACCATCGCACAA	88455
rs1058777	snp	A/C	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110028018	TTTCTATAAAGAGGC[A/C]CCTCGTTTATAATGG	88455
rs1510605	snp	C/T	0.351635	0.228408	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998104	GCAACTTAACGTTCT[C/T]CTTCTTCTTCATCAT	88455
rs1912516	snp	A/G	0.207864	0.246424	intron-variant	ANKRD13A	GRCh38.p7	12:110001637	AGGCCAGGGGTTGAA[A/G]CCAGCATGGCCAACA	88455
rs2136797	snp	A/G	0.0919752	0.193722	intron-variant	ANKRD13A	GRCh38.p7	12:110004063	TCAAGCGATTCTCCC[A/G]CCTCAGCCTCCCAAG	88455
rs2287173	snp	A/G	0.349671	0.229272	intron-variant	ANKRD13A	GRCh38.p7	12:110018899	GCTAATAAGAATGCA[A/G]ATTATTAAGAAAAAT	88455
rs2287174	snp	C/T	0.0922807	0.193971	missense, synonymous-codon	ANKRD13A	GRCh38.p7	12:110036265	GTCTTTGCCAGGAAC[C/T]TTCAGGACCAGCTTC	88455
rs2287175	snp	C/T	0.119281	0.213102	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037732	CCATCCAGGCTGCTC[C/T]CTGGGGTGGAGAAGG	88455
rs2302689	snp	A/G	0.318164	0.240528	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018370	TTCTAGAATATGCCC[A/G]AATGATGTCTGTCGC	88455
rs3759385	snp	C/T	0.0711525	0.174681	intron-variant	ANKRD13A	GRCh38.p7	12:110011934	AATGTGCTTGACAGA[C/T]ATTTCAAGTACAAAA	88455
rs3759386	snp	C/T	0.246769	0.249979	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998346	AGCTGTTCAAGAATC[C/T]CAACCTAATCCATTC	88455
rs4418866	snp	A/G	0.0479149	0.147179	intron-variant	ANKRD13A	GRCh38.p7	12:110007287	ACCTCAGTTTGGAGA[A/G]TTTTGTCATTTTAAC	88455
rs4766427	snp	A/G	0.0763149	0.179815	intron-variant	ANKRD13A	GRCh38.p7	12:110028807	CAGTGGCACGAACTC[A/G]GCTCACTGCAACCTC	88455
rs6606679	snp	C/T	0.401215	0.199083	intron-variant	ANKRD13A	GRCh38.p7	12:110010378	GGAAGATAATGAGTT[C/T]GCTAATTATTTCTTT	88455
rs6606680	snp	A/G	0.426201	0.177351	intron-variant	ANKRD13A	GRCh38.p7	12:110010451	TCTTGTTACTTTTAA[A/G]AAAATATTTAATGCA	88455
rs6606681	snp	C/T	0.240765	0.249829	intron-variant	ANKRD13A	GRCh38.p7	12:110013800	Aaataataataaata[C/T]aataatataataata	88455
rs7295290	snp	C/T	0.12932	0.218944	intron-variant	ANKRD13A	GRCh38.p7	12:110016585	AATCACTGATAGTCC[C/T]AGTTAAACACAACTG	88455
rs7295865	snp	A/T	0.00636936	0.0560724	intron-variant	ANKRD13A	GRCh38.p7	12:110002254	TTTGTAAACCTGGGG[A/T]TTGAGCTTTTTTGCT	88455
rs7299156	snp	C/T	0.354019	0.227333	intron-variant	ANKRD13A	GRCh38.p7	12:110002354	GGGCACGGTGGCTCA[C/T]GCCTGGAATCTCAGC	88455
rs7299483	snp	C/G	0.354019	0.227333	intron-variant	ANKRD13A	GRCh38.p7	12:110005001	GTATAAACATATACA[C/G]ATTGATtttttcaaa	88455
rs7300927	snp	A/G	0.429688	0.173817	intron-variant	ANKRD13A	GRCh38.p7	12:110020727	CCAGAAGGCAGAGGA[A/G]GCTGCCTTTTCTGCC	88455
rs7306815	snp	C/T	0.153997	0.230832	intron-variant	ANKRD13A	GRCh38.p7	12:110009450	tttaattcctgattt[C/T]agtaagttaagtctt	88455
rs7310558	snp	C/T	0.347032	0.230401	intron-variant	ANKRD13A	GRCh38.p7	12:110025070	TTACAAGACTACCAG[C/T]GGAGGCTGGGTGCAG	88455
rs7310812	snp	C/T	0.0205511	0.0992634	intron-variant	ANKRD13A	GRCh38.p7	12:110025263	ctggaggctgaggca[C/T]gagaatcgcttgaac	88455
rs7311261	snp	C/T	0.130694	0.219696	intron-variant	ANKRD13A	GRCh38.p7	12:110010600	ATCATGGGAGGTGTG[C/T]GGACTGGGCTCCAGG	88455
rs7954480	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110017976	CATTTGATACTCTGA[A/G]TGGTGGATATGACAA	88455
rs7970105	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110014191	gctgaggtgggtgga[C/T]cacgaggtcaggaga	88455
rs7970733	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110008750	attagccaggtgtgg[G/T]ggtgggcacctgtaa	88455
rs7970988	snp	G/T	0.0205511	0.0992634	intron-variant	ANKRD13A	GRCh38.p7	12:110008917	ggcctgcattttttt[G/T]ggtgggcagttttaa	88455
rs7976412	snp	C/G	0.429538	0.173972	intron-variant	ANKRD13A	GRCh38.p7	12:110012882	ATTATCAGGATTTCG[C/G]AACCAGTGGTAAGAA	88455
rs7976663	snp	C/T	0.154993	0.231244	intron-variant	ANKRD13A	GRCh38.p7	12:110020296	ATCCTGGACTTAGGC[C/T]TTCTTTTCTCTTGAT	88455
rs7977696	snp	A/G	0.36021	0.224397	intron-variant	ANKRD13A	GRCh38.p7	12:110008621	caggcatggtggctc[A/G]tgcctgtaatcccag	88455
rs9630308	snp	A/G/T	0.0212419	0.100845	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037630	TCAACCAGGGCCCTA[A/G/T]GGCTAAGGGCCTGCA	88455
rs10849627	snp	G/T	0.429087	0.174436	intron-variant	ANKRD13A	GRCh38.p7	12:110000433	AAGTTTGAGAATCAC[G/T]GGTTCTCAGGCTCCT	88455
rs11064671	snp	C/T	0.154661	0.231107	intron-variant	ANKRD13A	GRCh38.p7	12:110000714	ggcccccaaagccga[C/T]agcgtcttggttgag	88455
rs11064687	snp	A/G	0.160938	0.233598	intron-variant	ANKRD13A	GRCh38.p7	12:110003925	GCTCTTTGGGAGGCC[A/G]AGGCAGGTGGATCAT	88455
rs11064688	snp	C/T	0.160938	0.233598	intron-variant	ANKRD13A	GRCh38.p7	12:110004036	GGTGGCGGGTGCTTG[C/T]AATCCCAGCTACTTG	88455
rs11064702	snp	A/G	0.154329	0.23097	intron-variant	ANKRD13A	GRCh38.p7	12:110007692	GCCAGTTCTTCTTTA[A/G]TTTTTTTTAAACAAT	88455
rs11064715	snp	G/T	0.148326	0.228391	intron-variant	ANKRD13A	GRCh38.p7	12:110010397	AATTATTTCTTTCCT[G/T]CTAAACTTCAACTGA	88455
rs11064716	snp	A/G	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110010428	ATTTATAGTTCATAA[A/G]TTCATCGTCTTGTTA	88455
rs11064735	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110017946	caaaaaaaaaaaaaa[A/G]TGGCATACTTTAGAC	88455
rs11064797	snp	A/G	0.128632	0.218563	intron-variant	ANKRD13A	GRCh38.p7	12:110031808	catttccagttacta[A/G]tatatagaaatataa	88455
rs11352479	in-del	-/A	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110011109	GACCTTGTTTAAAAG[-/A]AAAAAAAAAAAAAGG	88455
rs11395070	in-del	-/T	0.429388	0.174127	intron-variant	ANKRD13A	GRCh38.p7	12:110005006	ACAGATTGATTTTTT[-/T]CAAAAGATTTTTATT	88455
rs11608607	snp	C/T	0.0228947	0.104514	downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039821	CTATATCTAAATAAG[C/T]GGGTATTAAAAACAA	88455
rs11831498	snp	A/G	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110006627	ttgagatggagtttc[A/G]ctcttgttgcctagg	88455
rs12231633	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026242	agtgctgagattaca[A/G]gcgtgagccaccgtg	88455
rs12231634	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026245	gctgagattacaggc[A/G]tgagccaccgtgcct	88455
rs12300179	snp	A/T	0.128632	0.218563	intron-variant	ANKRD13A	GRCh38.p7	12:110013320	TGGAGACACAGTTTG[A/T]CATCCTTGTGTGCCT	88455
rs12302340	snp	A/G	0.128632	0.218563	intron-variant	ANKRD13A	GRCh38.p7	12:110008873	ctgggcgacagagcg[A/G]gactcagtctggaaa	88455
rs12303589	snp	A/G	0.0150606	0.0854603	intron-variant	ANKRD13A	GRCh38.p7	12:110031566	atgttggctaggctg[A/G]tctggaactcctgac	88455
rs12312565	snp	A/G	0.124837	0.216412	intron-variant	ANKRD13A	GRCh38.p7	12:110011368	GGGATGGATGGAAGT[A/G]ACGCATGTGCACTTG	88455
rs12321161	snp	A/G	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110020780	ATGGGGAGGAACTGA[A/G]TGCCATCAGCAGGgc	88455
rs12425599	snp	C/G	0.110167	0.207236	intron-variant	ANKRD13A	GRCh38.p7	12:110029133	CTTTCCAAATAGAAT[C/G]TAGATTGGATGTAAG	88455
rs12810908	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110030861	gcactttgggaggcc[C/G]aggtgggtggatcac	88455
rs12824564	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110007653	cccaagtgctgggat[C/T]acaggtgtgagccac	88455
rs12825530	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026224	cccacctcggcctcc[C/G]aaagtgctgagatta	88455
rs12826903	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110026214	gtgatcctcacccac[A/C]tcggcctccgaaagt	88455
rs12826909	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026216	gatcctcacccacct[C/T]ggcctccgaaagtgc	88455
rs12826919	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110026231	cggcctccgaaagtg[C/T]tgagattacaggcgt	88455
rs12827625	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026234	cctccgaaagtgctg[A/G]gattacaggcgtgag	88455
rs28484840	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001452	TTTTTTTTTTTTTTT[C/T]TTTTTGAGATGGAGT	88455
rs34060026	snp	C/T	9.8894e-05	0.00703116	synonymous-codon, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033903	GCAAGATGAAGATTA[C/T]GAGATAATGCAGTTT	88455
rs34137720	in-del	-/C			downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039490	CTGGATGTACCCACA[-/C]CTTCCTGTTACGTAT	88455
rs34152716	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110033600	TTCGTTGTTTCCACT[-/A]AAAATCAAGGAAAAA	88455
rs34369572	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110003243	CTCTAGAGCCAGGCT[-/C]CCCTGTTTAGGAAGC	88455
rs34493523	snp	C/T	0.0114939	0.0749321	intron-variant	ANKRD13A	GRCh38.p7	12:110033056	GTTTTTTTCTTTTTC[C/T]TTTTTTTTTTTTTTT	88455
rs34501433	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110010476	AATGCAAGTTAGAGA[-/C]TAAGGTAAGAGAATC	88455
rs34586781	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110000755	TTCTTTCTTTCCTTC[-/T]TTTTTTTTTTTTTTT	88455
rs34589498	in-del	-/C			downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039568	AGGTGGCATGCTCCT[-/C]CCCAGCCTTCCTGCC	88455
rs34796332	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110025248	GTAATCCCAGCTACT[C/T]TGGAGGCTGAGGCAC	88455
rs35012464	in-del	-/A	0.109814	0.206997	intron-variant	ANKRD13A	GRCh38.p7	12:110017932	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGT	88455
rs35040415	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110011613	ATACTTCCTATTCTA[C/G]ACTTGAATGCTGATA	88455
rs35141236	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110012997	AGTCATGATCATCCT[-/G]GGTAAGGTTGGACTG	88455
rs35163441	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110009025	TCTGTAGGGATTTAT[-/A]CTTGTTCATCTAAGT	88455
rs35208482	in-del	-/C			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997558	TTAAAGGGTTGCGAG[-/C]ATGAAAATGAAGAAG	88455
rs35224948	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110018811	TGGCATTGCTCACCC[-/A]AATGTTGTGCATACA	88455
rs35362218	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110006109	GCATGAGCCACTGCA[-/C]CCCAGCCCCATGTAT	88455
rs35367681	snp	C/T	0.153997	0.230832	intron-variant	ANKRD13A	GRCh38.p7	12:110037055	CGAGGATTCATTTTA[C/T]GAAGACTTATACTTA	88455
rs35432632	in-del	-/A	0.000327445	0.0127912	intron-variant	ANKRD13A	GRCh38.p7	12:110023965	CTTAAGCTGGGGGGG[-/A]AAAAAACTATAAAGG	88455
rs35473330	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029003	GCCTCCCAAACTGCT[-/G]GGGATTACAGGCATG	88455
rs35525361	in-del	-/C			intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034259	CTTCATCATTTTCTA[-/C]GCACTGAAGCAGTAT	88455
rs35606471	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110028347	CTTCCTGTGTAGTTT[-/G]GGTGATATCCTCATA	88455
rs35629888	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110028403	TAGTGAATAGAACTT[-/C]CCCGGTCTTTAGCTG	88455
rs35732772	in-del	-/A			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997204	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	88455
rs35891499	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110035066	TGGCCCCATTCCCAG[-/C]ACCCATTCAGTTTTC	88455
rs35945468	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110015688	GTAGCTAGGATTACA[-/G]GGCGTGTGCCACCAT	88455
rs36049730	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029439	CTTTTCCCATCTGGT[-/G]GGAGATGACCTCAGT	88455
rs36087331	snp	C/T	0.000808934	0.0200951	synonymous-codon, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033921	GATAATGCAGTTTGC[C/T]ATCCAGCAAAGTCTG	88455
rs55737380	snp	C/G	0.140242	0.224618	intron-variant	ANKRD13A	GRCh38.p7	12:110012787	AGGGATACTGTAGGC[C/G]AAGCCCTGCCTGCCA	88455
rs56249481	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110019694	CGTGGAGTTTCTGGA[A/G]GTTAGAATTGACCCA	88455
rs56960173	snp	A/G	0.351635	0.228408	intron-variant	ANKRD13A	GRCh38.p7	12:110005654	TGGCATGTTTCAGGT[A/G]CTTAATTCCTTTTTA	88455
rs56972807	snp	A/G	0.349671	0.229272	intron-variant	ANKRD13A	GRCh38.p7	12:110036540	GGATCACGAGGTCAG[A/G]AGATTGAGACCATCC	88455
rs57109511	snp	C/T	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110003896	GGGCACGGTGGCTCA[C/T]GCCTGTACTCCCAGC	88455
rs57285442	snp	A/G	0.0275645	0.114116	intron-variant	ANKRD13A	GRCh38.p7	12:110009609	ACTCTTTATGCACTT[A/G]TTGTTTTAAAATCAC	88455
rs57307003	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110030892	CTGAGGTCGGGAGTT[C/T]GAGACCAGCCTGACC	88455
rs57684892	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110021740	CCCTCTCTCATTTTT[A/T]GATGGTCACTTTTCC	88455
rs57966967	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002388	TTGGGAGGCTGAGGC[A/G]GGCAGATCGCCTGAG	88455
rs58064813	snp	C/G	0.347253	0.230308	intron-variant	ANKRD13A	GRCh38.p7	12:110008496	ATCAGGATAATAGTG[C/G]GTTCATAAAATGAAT	88455
rs58712773	snp	A/G	0.0182019	0.0936463	intron-variant	ANKRD13A	GRCh38.p7	12:110032152	GGTTCTAGGGGAGGA[A/G]GGATTGTTGTGCCAT	88455
rs59262099	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110021443	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	88455
rs59298751	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110030885	GGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG	88455
rs59392277	snp	A/C	0.0711525	0.174681	intron-variant	ANKRD13A	GRCh38.p7	12:110011495	AAGGCACGTGGAACT[A/C]AATACACAATAATGA	88455
rs59470102	snp	A/G	0.0123036	0.0774623	intron-variant	ANKRD13A	GRCh38.p7	12:110010747	TCTTCACTGTATAAT[A/G]GCCATGACATAGTTT	88455
rs59547241	snp	G/T	0.350982	0.228698	intron-variant	ANKRD13A	GRCh38.p7	12:110037178	TGGTCTTGGGCAAGA[G/T]TGTGGGGTTTCTCAC	88455
rs59591754	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110021909	CAAACAAAATATTCC[C/T]TGCCACCTTCATAGC	88455
rs59713918	snp	C/G/T	3.29603e-05	0.00405944	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019201	ACCACCGAACGCTTC[C/G/T]ACCTTTCCCAAGAAA	88455
rs59799011	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110000941	TTTGTATTTTTAGTA[A/G]AGATGGGGTTTCTCC	88455
rs60149107	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110002266	GGATTGAGCTTTTTT[-/T]GCTCTATATTCCAGT	88455
rs60325242	snp	C/T	0.0205511	0.0992634	intron-variant	ANKRD13A	GRCh38.p7	12:110004612	CTCCAGCCTGGGCAA[C/T]AAGAGGGAGACTCTG	88455
rs60340521	snp	C/T	0.00361536	0.0423628	intron-variant	ANKRD13A	GRCh38.p7	12:110013100	AGAAAGTATGAGAAT[C/T]AAATTTCACCCTTTT	88455
rs60393726	snp	G/T	0.00478085	0.0486577	intron-variant	ANKRD13A	GRCh38.p7	12:110032774	ATTGAAAATAAAAAT[G/T]TATAGCTATGTGCGT	88455
rs60402438	snp	A/G	0.0718919	0.175435	intron-variant	ANKRD13A	GRCh38.p7	12:110022221	TTGGGAGGCTGAGGC[A/G]GGTGGATCACGAGGT	88455
rs60806405	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110025615	TCCTAATGATAGTTA[A/T]CCATTTCTCATTTTT	88455
rs60844638	snp	A/T	0.0146672	0.084371	intron-variant	ANKRD13A	GRCh38.p7	12:110027642	AAACTTTAATGAAGA[A/T]CTTTTTTTTATAGCC	88455
rs61046935	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110031880	TTATCTTTTTTTTTT[-/T]CTTACACAATTGCAT	88455
rs61113301	snp	C/G	0.239902	0.249796	intron-variant	ANKRD13A	GRCh38.p7	12:110001105	CTGGGAGGTATTGGT[C/G]CCCTCAAGTTTCAAG	88455
rs61608023	snp	A/G	0.0178098	0.0926698	intron-variant	ANKRD13A	GRCh38.p7	12:110016713	CTCCTTTTGTCATTT[A/G]TAGCCGACATCTATA	88455
rs61940908	snp	A/T	0	0	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997231	AAAAAAAAAAAAAAT[A/T]AGCCGGGCGTGGTGG	88455
rs61940909	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110024408	TCATTCCCTTAATTA[A/T]TTAAAAAAAAAAAAG	88455
rs61940910	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110026596	AAAAAAAAAAAAATT[A/T]CCTGGCTGAGCACGG	88455
rs61940911	snp	C/T	0.0471551	0.14613	intron-variant	ANKRD13A	GRCh38.p7	12:110029339	GCCCTAGACATTTGA[C/T]CTTTAATAGGTCTGA	88455
rs61940912	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110030810	ATTTAAAAAAAAATT[A/T]ATGGCCGGACGTGGT	88455
rs71452563	snp	A/G	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110030867	TGGGAGGCCAAGGCG[A/G]GTGGATCACCTGAGG	88455
rs71458316	snp	A/C	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110032739	TTGTGCTCTATTAAT[A/C]CAACAGAATAACATA	88455
rs71458317	snp	C/T	0.0236746	0.106192	intron-variant	ANKRD13A	GRCh38.p7	12:110036644	GTAGTCTCAGCTACT[C/T]GGGAGGCTGAGGCAG	88455
rs71947957	in-del	-/A			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997205	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	88455
rs73205044	snp	A/G	0.128632	0.218563	intron-variant	ANKRD13A	GRCh38.p7	12:110004315	AAAACCTAAATGATC[A/G]GTTTCGAAAGTGAAT	88455
rs73205045	snp	C/T	0.00597247	0.0543191	intron-variant	ANKRD13A	GRCh38.p7	12:110006895	GCCAATGAGCTCAGC[C/T]AAAATTTTGTTCTTT	88455
rs73205046	snp	C/T	0.128632	0.218563	intron-variant	ANKRD13A	GRCh38.p7	12:110010273	TTTTACACACCTCCC[C/T]TGTGGCAGGTAGTAT	88455
rs73404616	snp	C/T	0.00755907	0.0610114	intron-variant	ANKRD13A	GRCh38.p7	12:110012742	TAAGCTCTTCTACCA[C/T]TGGCCAGAGTAATTT	88455
rs73404622	snp	A/G	0.0115144	0.0749975	intron-variant	ANKRD13A	GRCh38.p7	12:110015104	TGAAGGGTAACTTTT[A/G]GATTTCTGAATCTTT	88455
rs73404630	snp	C/T	0.00914312	0.0669923	intron-variant	ANKRD13A	GRCh38.p7	12:110022145	GTTGAATAACTAAAC[C/T]GCTTCCAAGAGTGGA	88455
rs74654926	snp	C/T	0.152334	0.230133	intron-variant	ANKRD13A	GRCh38.p7	12:110034904	CTCTGGGAAGCAGCC[C/T]CTGCCCTCACAGGGC	88455
rs74725620	snp	G/T	0.101301	0.200969	intron-variant	ANKRD13A	GRCh38.p7	12:110001830	ATATGACACATGCCC[G/T]CAGACTAAATGATTC	88455
rs74731825	in-del	-/TTT			intron-variant	ANKRD13A	GRCh38.p7	12:110016292	TCTCTTTTTTTTTTT[-/TTT]AACCCAGGGTTTTTA	88455
rs74842404	snp	G/T	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110005800	GTAACGCTGCTGTGT[G/T]TATTTGTGTATATGT	88455
rs74842658	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110035790	GTATGGTGGTGTGCA[C/T]CTGTATTCCCAACTA	88455
rs74892296	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110034729	CTTCTGTGCCTCCTG[A/G]CTCTACTAGGGTAGG	88455
rs74917245	snp	C/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110026517	GGCAGGCGGAGGTTT[C/T]GGTGAGCTGAGATCG	88455
rs74976836	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110034732	CTGTGCCTCCTGGCT[C/G]TACTAGGGTAGGGTC	88455
rs74981675	snp	A/T	0	0	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997229	AAAAAAAAAAAAAAA[A/T]TTAGCCGGGCGTGGT	88455
rs75116289	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110012276	AGGCTGAGGGGGTAG[C/G]ATCACCTGAGCCCGG	88455
rs75196647	snp	G/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110021444	TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT	88455
rs75222879	snp	C/T	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110016283	TTCTTATTTTCTCTT[C/T]TTTTTTTTTTTAACC	88455
rs75251086	snp	A/G	0.030278	0.119257	intron-variant	ANKRD13A	GRCh38.p7	12:110032361	TAGGAGGAATTAAAA[A/G]ATAGCATTTTAATGT	88455
rs75403765	snp	C/T	0.00795532	0.062565	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038489	CACCTAGGAAGAGCC[C/T]GCATGCCCTAGACTC	88455
rs75584653	snp	C/T	0.0329836	0.124112	intron-variant	ANKRD13A	GRCh38.p7	12:110021680	TCTGCCTACTTTGGC[C/T]TCCCAAAGTTCTGGG	88455
rs75587535	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110003493	TTCCACTGACTCAGC[A/G]TGGGGGCCACACAGG	88455
rs75721411	snp	C/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110015970	TTTTTTTTTTTTTTC[C/T]ATACAGTATCTCGCT	88455
rs75803899	snp	A/C	0.00199481	0.0315187	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038982	TACTGTTCCAGGTAA[A/C]GTCTGTATCATACAG	88455
rs75891377	snp	A/G	0.00536754	0.0515263	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033828	CTTTGAGGTTGATCA[A/G]TCTGTGTTTGAAATT	88455
rs76046239	snp	A/C	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110036750	GCGAGACTCCGTCTC[A/C]AAAAAAAAAAAGACT	88455
rs76052549	snp	A/C	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110017793	AAAAATTAGCCGGGC[A/C]TGATGGTGGGTGCCT	88455
rs76358958	snp	A/C	0.110872	0.20771	intron-variant	ANKRD13A	GRCh38.p7	12:110005308	TACCACGCTTGGCTA[A/C]TTTTTAAAGATTTTT	88455
rs76440971	in-del	-/AA			intron-variant	ANKRD13A	GRCh38.p7	12:110024421	TATTTAAAAAAAAAA[-/AA]GGAAGAGGAAGGATT	88455
rs76614047	snp	A/T	0.000752278	0.0193797	intron-variant	ANKRD13A	GRCh38.p7	12:110024143	TAAAATAAGATTTAA[A/T]ATAGCTATTTAGCTT	88455
rs76623901	in-del	-/GTAA			intron-variant	ANKRD13A	GRCh38.p7	12:110022602	TGAGGTGGAGCAGAC[-/GTAA]TCATCTTTCCATCCA	88455
rs76696441	snp	C/T	0.00517822	0.0506191	intron-variant	ANKRD13A	GRCh38.p7	12:110001709	ACAGGCATGAGCCAC[C/T]GTTGCCGGCCTTTTT	88455
rs76714189	snp	A/G	0.5	0	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997378	AGCGAGACTGTCTCA[A/G]AAACAACTTCAACAA	88455
rs76772513	snp	C/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110026525	GAGGTTTTGGTGAGC[C/T]GAGATCGTGCCATTG	88455
rs76803350	snp	G/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110033071	TTTTTTTTTTTTTTT[G/T]TTGAGACAGTCTTAC	88455
rs76838729	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110034733	TGTGCCTCCTGGCTC[A/T]ACTAGGGTAGGGTCT	88455
rs76860408	snp	G/T	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110015616	GAATAGTGCTATCTC[G/T]GCTCATGGCAACCTC	88455
rs76904708	snp	C/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110026538	GCTGAGATCGTGCCA[C/T]TGCACTCCAGCCTGG	88455
rs77123010	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001391	ATATTTAAGGTGGTT[A/G]AGCCCTCACCGAAGT	88455
rs77145654	snp	A/T	0.0189856	0.0955633	intron-variant	ANKRD13A	GRCh38.p7	12:110026593	AAAAAAAAAAAAAAA[A/T]TTTCCTGGCTGAGCA	88455
rs77148745	snp	A/G	0.0228947	0.104514	intron-variant	ANKRD13A	GRCh38.p7	12:110022485	GCAAATGCTTAGGGC[A/G]GTAGAGGCAGGATTG	88455
rs77565582	snp	G/T	0.00835141	0.0640778	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038594	AGGGAAAATAATGAT[G/T]CCACGTTGCTTTTTA	88455
rs77567091	snp	C/T	0.02016	0.0983543	intron-variant	ANKRD13A	GRCh38.p7	12:110020212	ATTATCCTTATAGTA[C/T]TTGTCTAGAATGCCA	88455
rs77637869	snp	A/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110004894	AAGGTAGGTTTTTTT[A/T]ATTGTTCAGTTTTAC	88455
rs77738139	snp	C/T	0.0170251	0.090679	intron-variant	ANKRD13A	GRCh38.p7	12:110011406	CTTTGTGAGTAGATC[C/T]GCATACGTGCCCGGC	88455
rs77915874	snp	C/T	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110015968	CTTTTTTTTTTTTTT[C/T]CCATACAGTATCTCG	88455
rs78140462	snp	C/T	0.0162398	0.0886349	intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110032554	GAATAAAACATTCGG[C/T]ATTACTGTATAAACT	88455
rs78161819	snp	A/G	0.0471551	0.14613	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997788	TTTTTCTTCATATGC[A/G]TGGAATTTGAGAATA	88455
rs78182757	snp	A/G	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110016534	CATGTATTTTTTTTT[A/G]GTCAAGGAAATACAT	88455
rs78185560	snp	A/G	0.0150606	0.0854603	intron-variant	ANKRD13A	GRCh38.p7	12:110028407	TGAATAGAACTTCCC[A/G]GTCTTTAGCTGGTTA	88455
rs78255092	snp	A/G	0.0707826	0.174302	intron-variant	ANKRD13A	GRCh38.p7	12:110017553	ATGACATAAAAGTAC[A/G]TAAAAGAATAGAACT	88455
rs78256648	snp	A/G	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110026554	TGCACTCCAGCCTGG[A/G]CAACAAGAGTGAAAC	88455
rs78337612	snp	C/T	0.0205511	0.0992634	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037875	CCAATCCCCGCAGGT[C/T]TGTAGATAAATTTTT	88455
rs78524076	snp	G/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110030184	TCTCTTTTTTTTTTT[G/T]GAGATGGAGTCTCGC	88455
rs78549167	snp	G/T	0.0185938	0.0946107	intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110032621	CCCTAAAGAAAGTTA[G/T]GCACATGAGCATCTG	88455
rs78739280	snp	C/T	0.110519	0.207473	intron-variant	ANKRD13A	GRCh38.p7	12:110032890	AGTTCACAAACAGGC[C/T]AATACAAACTATTAG	88455
rs78750852	snp	G/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110030185	CTCTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT	88455
rs78831162	snp	A/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110016533	ACATGTATTTTTTTT[A/T]AGTCAAGGAAATACA	88455
rs78873143	snp	C/G/T	0	0	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037823	TAGCTGTATTGGCTT[C/G/T]CAGGTCACATTTTTA	88455
rs78960397	snp	A/G	0.00716266	0.059414	intron-variant	ANKRD13A	GRCh38.p7	12:110005764	GACATTTGGGTTGTC[A/G]CCACTTTTTGGCTAT	88455
rs79051683	snp	A/G	0.0225045	0.103662	intron-variant	ANKRD13A	GRCh38.p7	12:110003797	GGAGGCTGAGGTGGG[A/G]TCAGTGCTTGAGGAC	88455
rs79189647	snp	A/C	0.00751507	0.0608363	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037421	GCGCCCTGAGCGAGA[A/C]AAGCCGTTTTGATAA	88455
rs79225340	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110000221	AGGAAGGGCTTGGTT[A/G]GTTTTGGAGTCCAGG	88455
rs79256362	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110034731	TCTGTGCCTCCTGGC[A/T]CTACTAGGGTAGGGT	88455
rs79504243	snp	A/G	0.0383028	0.132986	intron-variant	ANKRD13A	GRCh38.p7	12:110036342	AGGTGATTGACTGAC[A/G]TGACTCTGGAATAAA	88455
rs79667456	snp	A/C	0.0138799	0.0821421	intron-variant	ANKRD13A	GRCh38.p7	12:110036948	TGAATGATGTATGAT[A/C]ACAGGGCCTAGATGT	88455
rs79820539	snp	A/C	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110001468	TTTTTGAGATGGAGT[A/C]TCGCTCTGTCATTCA	88455
rs79923065	snp	C/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110026531	TTGGTGAGCTGAGAT[C/T]GTGCCATTGCACTCC	88455
rs80209452	snp	G/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110026516	TGGCAGGCGGAGGTT[G/T]TGGTGAGCTGAGATC	88455
rs80228443	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110019759	AGATTCACACTTACT[A/G]TATAGTTAAATGTTT	88455
rs111243781	in-del	-/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110030173	ATAACTCATTTTCTC[-/T]TTTTTTTTTTTGAGA	88455
rs111303862	snp	C/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110029108	AGTAGATTGTCCATG[C/T]TATTAGCTCCTTTCC	88455
rs111313070	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033354	GGCGTGAGCCACCGC[A/G]CCCGGCAGTTATTGA	88455
rs111319019	snp	A/C	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110018043	TGTGAGTGAGGAAGG[A/C]CAGATGTACAGACCT	88455
rs111325891	snp	A/G	0.00478085	0.0486577	intron-variant	ANKRD13A	GRCh38.p7	12:110026065	CTCCTGGGTTCAAGT[A/G]ATTCTCCTGCCTCAG	88455
rs111400359	snp	A/G	0.5	0	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033808	TCAGCTTCCCACATC[A/G]CAAACTTTGAGGTTG	88455
rs111428999	snp	A/G	0.0107246	0.0724382	intron-variant	ANKRD13A	GRCh38.p7	12:110015983	TCCATACAGTATCTC[A/G]CTCTGTTGCCCAGGC	88455
rs111796339	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032119	AGTGGTAGGAATGGC[C/T]GTCCTTGTCTTGTTC	88455
rs111799646	snp	A/C	0.0120273	0.0766093	intron-variant	ANKRD13A	GRCh38.p7	12:110037329	TGATGATAGTAGTGA[A/C]TCTCCCTTTTTATCT	88455
rs111931974	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110029257	ATTAAGGCTTTGATC[A/G]TGGCAGGTTGTCATG	88455
rs112037652	snp	A/C/G	0.5	0	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039342	AAAAAGGGACTGAGC[A/C/G]TTGTGTCAACCTGTT	88455
rs112192220	snp	C/G	0.5	0	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038946	ATTGTGCTTCTTTGG[C/G]GATAGGAAGAGAAAC	88455
rs112223294	in-del	-/T	0.152334	0.230133	intron-variant	ANKRD13A	GRCh38.p7	12:110035446	CCTATATCTACCAAA[-/T]TTTTTTTTTTTTTTA	88455
rs112277486	snp	C/T	0	0	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037798	GGAGGAGAGCATCAT[C/T]ACTTTCCATTAGCTG	88455
rs112291985	snp	A/G	0.0119091	0.0762411	intron-variant	ANKRD13A	GRCh38.p7	12:110015068	GGCGTGAGCCAGTGC[A/G]CCCGGCCGCATTTCT	88455
rs112292669	snp	G/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110031237	AAGCAAAAAAAAACT[G/T]GTAGAATATATATGA	88455
rs112438783	snp	A/C	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110001241	TTTTTGAATGGCTCA[A/C]AATTGGTGCTATAAT	88455
rs112451730	snp	A/G	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110028702	AAATTGTGCTGTTTT[A/G]TGGTGTTATGTTGGA	88455
rs112536062	snp	C/T	0.00438332	0.0466095	intron-variant	ANKRD13A	GRCh38.p7	12:110011567	TATTCTGACCCAAAT[C/T]ATCTGTGCTTTCAGT	88455
rs112537960	snp	A/G	0.5	0	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037387	AGCCTCCTCACCAGC[A/G]CAGAAGGCCTGTGCC	88455
rs112765872	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033163	GGTTCATGCCATTCT[C/T]CTGCCTCAGCCTCCC	88455
rs112810261	snp	A/G	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110028761	ATTTTTTTTTCAGAC[A/G]GAGTCTCGCTCTGTC	88455
rs112846454	in-del	-/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110031358	TGATGGTTCAGTGCA[-/T]TTTTTTTTTTTTTCT	88455
rs113007415	snp	A/G	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110016719	TTGTCATTTATAGCC[A/G]ACATCTATATTATTA	88455
rs113022189	snp	A/G	0.00438332	0.0466095	intron-variant	ANKRD13A	GRCh38.p7	12:110011487	GCTACTTCAAGGCAC[A/G]TGGAACTCAATACAC	88455
rs113189922	snp	C/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110028760	TATTTTTTTTTCAGA[C/T]GGAGTCTCGCTCTGT	88455
rs113236084	snp	A/G	0.0134861	0.0810011	intron-variant	ANKRD13A	GRCh38.p7	12:110009708	GTCTGAAGAGTTACA[A/G]TTATCCAAGAAATGT	88455
rs113251679	snp	C/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110016450	TGAGTGGCTGTGGGC[C/T]CGTTATTTATTTCTC	88455
rs113289184	in-del	-/TGT	0.225597	0.248806	intron-variant	ANKRD13A	GRCh38.p7	12:110036095	TACCTCCCACTTAGG[-/TGT]TGTTTTTGAGGTAAC	88455
rs113304602	snp	C/T	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110033714	TTGAGCCTTTCTTTT[C/T]TTTCTAATGTACAAC	88455
rs113318525	snp	A/G			splice-acceptor-variant, missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028510	GAGTTCTGGCTCAGC[A/G]GGACCTCACCACGGA	88455
rs113360622	snp	C/T	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110028800	TGGAGTGCAGTGGCA[C/T]GAACTCGGCTCACTG	88455
rs113400204	snp	C/T	0.0115144	0.0749975	intron-variant	ANKRD13A	GRCh38.p7	12:110022387	CCAGGAGGCGGAGCT[C/T]TCGGTGAGCTGAGAT	88455
rs113522015	snp	A/G	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110027306	AGCCTTTAGAATGGC[A/G]CCTGCAGTATGTGGT	88455
rs113537759	in-del	-/T	0	0	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039069	TCACAATCTGTTTTG[-/T]TTTTTTTTTTTTGTC	88455
rs113577418	snp	A/G	0.0205511	0.0992634	intron-variant	ANKRD13A	GRCh38.p7	12:110027875	CTCTATGTAAAGGCC[A/G]AAGATACCCCCAAGC	88455
rs113661835	in-del	-/A	0.5	0	intron-variant	ANKRD13A	GRCh38.p7	12:110036749	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAGAC	88455
rs113816710	snp	A/G	0.140581	0.224783	intron-variant	ANKRD13A	GRCh38.p7	12:110014909	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	88455
rs113908078	snp	A/G	0.00755907	0.0610114	intron-variant	ANKRD13A	GRCh38.p7	12:110017052	GTGCTGGGATTACAG[A/G]CATGAGCTACCATGC	88455
rs113969637	snp	C/T	0.0425829	0.139564	intron-variant	ANKRD13A	GRCh38.p7	12:110020422	ATCCTTTTCTTCTAA[C/T]TTAGATTGAGCTGTG	88455
rs114771567	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110032788	TTTATAGCTATGTGC[A/G]TCAAAACTGTTGAAT	88455
rs115022055	snp	A/G	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110021018	GGGTGACAATTCCTG[A/G]CTGTTACCCCACTGA	88455
rs115696247	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110022618	TAATCATCTTTCCAT[C/T]CATCAGAAGAGTCTG	88455
rs115705265	snp	G/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110006308	TTCTTCACATCCTTG[G/T]CAACACTTGGTATTA	88455
rs115981662	snp	A/C	0.0256215	0.110247	intron-variant	ANKRD13A	GRCh38.p7	12:110013375	AATATGAAATACTCA[A/C]TACCAATCACATTAT	88455
rs116205953	snp	C/T	0.0271762	0.113356	intron-variant	ANKRD13A	GRCh38.p7	12:110023755	CTTTGGGACTGCTGT[C/T]CAATAAATGTCACCA	88455
rs116251419	snp	C/T	0.0182019	0.0936463	intron-variant	ANKRD13A	GRCh38.p7	12:110007124	TAGTACGTTTTAAAA[C/T]TGGCAAGCGTGAAAT	88455
rs116260683	snp	C/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110032940	GCTCCAGAGAAGAGC[C/T]AGGCAGTGTAAACAA	88455
rs116420465	snp	A/G	0.0123036	0.0774623	intron-variant	ANKRD13A	GRCh38.p7	12:110012476	CTTGGGACAAGGGAT[A/G]GGGACAAGGAAATGG	88455
rs116732860	snp	G/T	0.0383715	0.133092	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034190	TCTTCAGGCAGACTT[G/T]CCTTTTCCTCATATT	88455
rs117102604	snp	C/T	0.0165278	0.0893908	intron-variant	ANKRD13A	GRCh38.p7	12:110011418	ATCCGCATACGTGCC[C/T]GGCAGATCATGCTTG	88455
rs117120831	snp	A/G	0.00716266	0.059414	intron-variant	ANKRD13A	GRCh38.p7	12:110012881	CATTATCAGGATTTC[A/G]CAACCAGTGGTAAGA	88455
rs117355755	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038918	CCTCCTCCATTTTGC[A/G]TCTATTTCTTCTATT	88455
rs117398522	snp	A/C	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110022640	AAGAGTCTGTGCCAG[A/C]AAACAGTGACTTCCT	88455
rs117478133	snp	C/T	0.0383715	0.133092	intron-variant	ANKRD13A	GRCh38.p7	12:110006965	AAGGACAGTTCTTTC[C/T]CAATGAATTATTTTG	88455
rs117478690	snp	A/G	0.110519	0.207473	intron-variant	ANKRD13A	GRCh38.p7	12:110006870	CAAAGTGCTGGGATT[A/G]TAGGGATGAGCCAAT	88455
rs117626110	snp	A/T	0.0225045	0.103662	intron-variant	ANKRD13A	GRCh38.p7	12:110014085	ATAGAGAAAAATTAA[A/T]AGCTCTATCGAGAAA	88455
rs117773557	snp	C/T	0.0150606	0.0854603	intron-variant	ANKRD13A	GRCh38.p7	12:110032276	TACCATTTTTAAGTA[C/T]TGATTTTTGTGAGAT	88455
rs117996860	snp	C/G/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110018222	GAAAGCCAAGAAGTC[C/G/T]GTTGTTTGATGGTCA	88455
rs118048073	snp	C/T	0.121369	0.214369	intron-variant	ANKRD13A	GRCh38.p7	12:110031489	CCAAGTAGCTGGGAA[C/T]ACAGGTGCGTGCCAC	88455
rs137904219	snp	C/T	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110032722	GATGGTAGAATGCGC[C/T]ATTGTGCTCTATTAA	88455
rs137978713	snp	A/T	0.0494327	0.149241	intron-variant	ANKRD13A	GRCh38.p7	12:110016883	ATTCAAGCGATTCTC[A/T]TGCCTCAGCTTCCTG	88455
rs138015304	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110021106	TATTTTTGTGCCCAC[A/G]GGGTTTTCAGAGTTC	88455
rs138034856	snp	A/C/T	0.00186315	0.0304651	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033830	TTGAGGTTGATCAAT[A/C/T]TGTGTTTGAAATTCC	88455
rs138087396	snp	C/T	0.00517822	0.0506191	intron-variant	ANKRD13A	GRCh38.p7	12:110027285	TTAGATGAGTTACGA[C/T]GTGGAAGCCTTTAGA	88455
rs138205745	snp	A/T	0.00636936	0.0560724	intron-variant	ANKRD13A	GRCh38.p7	12:110004420	CGGGAGTTCGAGACC[A/T]ACCTGACCAACACAG	88455
rs138362243	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039119	TCTGCACATGAGGCC[A/G]GTATAGGCAACGTCA	88455
rs138415560	snp	C/T	0.0471551	0.14613	intron-variant	ANKRD13A	GRCh38.p7	12:110021499	GGCACGATCTTGGCT[C/T]ACTGCAACCTCCGCC	88455
rs138423067	in-del	-/TTGGTG	0.0205511	0.0992634	intron-variant	ANKRD13A	GRCh38.p7	12:110024665	AGGGATTGATGGCTT[-/TTGGTG]TTGGAGCCCAGTGCT	88455
rs138438848	snp	A/G	9.88777e-05	0.00703058	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012033	TGGACCCACGAGGTC[A/G]AACATTATTGCATCT	88455
rs138450238	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110006155	TATATGTTTTCATTT[A/G]TCTTGGGTATATACC	88455
rs138468554	snp	A/G	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110010868	TTCAGAGACTGCAGG[A/G]GTAGTTAGTACCTGA	88455
rs138683846	snp	A/T	1.98702e-05	0.00315194	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030751	GGAAGGGACCCAGGC[A/T]GATTCAGGTAAAAAA	88455
rs138719507	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028245	CATGCACTTTCAGAT[A/C]TTTCTTTCTTTTTTT	88455
rs138750062	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033381	TTGATAGTGTTCTGT[G/T]TCTTAGGCTAGGTGA	88455
rs138813949	snp	A/G	0.0111196	0.0737302	intron-variant	ANKRD13A	GRCh38.p7	12:110033671	CTCAGAATCTCTCAT[A/G]TAATAGTAAGCCTTG	88455
rs138836219	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110009920	CCCAGGCTGGAATGC[A/G]ATGGCACAATCTCAG	88455
rs138912432	snp	C/T	0.0372196	0.131242	intron-variant	ANKRD13A	GRCh38.p7	12:110016282	CTTCTTATTTTCTCT[C/T]TTTTTTTTTTTTAAC	88455
rs139164318	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998022	CTCTGGTAAGCAAAA[C/T]GATGTGGTTCCTGTC	88455
rs139211423	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110000393	GCATTTTTAACAAAC[C/T]CCCCAGGGAGGCTGA	88455
rs139352104	snp	C/T	0.00557542	0.0525036	intron-variant	ANKRD13A	GRCh38.p7	12:110036170	TCATGGAAAGACTTT[C/T]AATTTGGTTCTTGCT	88455
rs139496274	snp	A/G	0.0154538	0.0865337	intron-variant	ANKRD13A	GRCh38.p7	12:110007437	CCAGGCTGGAGTTCA[A/G]TGGCACAATCTTGGC	88455
rs139503139	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110011669	AGTGTTGTCCGGTGA[C/T]TGCATTTCATGAAAG	88455
rs139554422	snp	A/G	1.65269e-05	0.00287457	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037480	GCCAAAGAGCTGGAG[A/G]AATGGGAGCTCCGGC	88455
rs139588972	snp	C/G	0.00478085	0.0486577	intron-variant	ANKRD13A	GRCh38.p7	12:110018833	GTGCATACATAATTT[C/G]TGTGAATTCTGTAAT	88455
rs139608370	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012515	GATGATGCAGGTTGC[A/G]TCCCAGGCCAGAAAC	88455
rs139619351	snp	A/G	3.29571e-05	0.00405924	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025782	TGATCACCAAAATAC[A/G]CACAGAACATCTGAC	88455
rs139629684	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110023452	TTTTTCACATCCTTT[A/G]CCCTGCTGCACCAAA	88455
rs139699900	snp	A/G	1.64773e-05	0.00287026	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013172	GAGATGGTGTACACA[A/G]TTCTCCAACATCGAG	88455
rs139706960	snp	A/G	0.000312967	0.0125054	intron-variant	ANKRD13A	GRCh38.p7	12:110024161	AGCTATTTAGCTTCT[A/G]TGCAAATGAGGAATC	88455
rs139862935	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110030518	GTGTATTGGGAAGGG[C/T]TGTTATGAGGCTTAA	88455
rs139905170	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110034525	TATTGCACCCTCAAA[C/T]TCCTGGGTTCAAGAG	88455
rs140105280	snp	G/T	0.0119091	0.0762411	intron-variant	ANKRD13A	GRCh38.p7	12:110026812	GCTTGAACCCCAGAG[G/T]TGGAGGTTGCTGTGA	88455
rs140164303	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998950	ATGAAGTAGAAATAT[A/C]CCCTTTTATGCAAAT	88455
rs140508986	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010499	AGAGAATCTAGAAGA[C/T]ATTAATATGACTTGG	88455
rs140545018	snp	A/G	0.00478085	0.0486577	intron-variant	ANKRD13A	GRCh38.p7	12:110014329	AGGCAGGAGAATGCT[A/G]TGAACCTGGGAGGCG	88455
rs140559689	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110020544	AGTCCTCTTCTGCCA[A/G]CCTCCTTGCACTGGC	88455
rs140833944	snp	C/T	0.0138799	0.0821421	intron-variant	ANKRD13A	GRCh38.p7	12:110036515	AGCATTTTGGGAGGC[C/T]GAGGCAGGCGGATCA	88455
rs140991420	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035586	TCCCGAGTAGCTGGG[A/T]TTACAGGTGCGCACC	88455
rs141072526	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110015137	GAACTTACAGGAATG[A/G]TAGGTAAGAAAATAA	88455
rs141182055	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011472	TGCTGGAGTTTATGT[A/G]CTACTTCAAGGCACG	88455
rs141333386	snp	A/G	0.000313131	0.0125087	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028523	GCAGGACCTCACCAC[A/G]GAATGTGCTACTGCA	88455
rs141384693	snp	C/T	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110017384	TTCTCTAAAGTATTA[C/T]GTAGGCAGTTGACTG	88455
rs141719454	snp	A/G	3.30726e-05	0.00406635	intron-variant	ANKRD13A	GRCh38.p7	12:110028486	TCATTTGGCATTTCT[A/G]ACTCTCCTGAGTTCT	88455
rs141725150	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038259	CATCACCTCACTGCA[C/T]GCATCGAAGGATCTG	88455
rs141771343	snp	A/G	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110033545	GGGGGAGAAATCTGC[A/G]CTTTTCATTTTATAG	88455
rs141807942	snp	A/G	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110024576	TGTAATAGTGGAGAC[A/G]ATTGTTGATCCAGTC	88455
rs141829613	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998597	CTTCATATTCGCAGA[C/T]TGTGGTCAAATATGT	88455
rs142148269	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110008956	ATTCAATCTCTTGTT[A/G]TAAACTTATTCAGAT	88455
rs142171033	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:109999885	CTCTGTCCCCGGGAT[C/T]CCCAGACCCCTTCCA	88455
rs142204358	snp	G/T	0.00557542	0.0525036	intron-variant	ANKRD13A	GRCh38.p7	12:110008860	ACTATACTCCAGCCT[G/T]GGCGACAGAGCGAGA	88455
rs142207086	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110005968	ATTACAGGTGTGCAC[C/T]ACCACGCCTGGCTAA	88455
rs142252344	snp	C/T	0.000774944	0.0196691	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019267	AGCAGGGAAGTTGAG[C/T]GGCGGCTCACAAGCC	88455
rs142275624	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110030269	CCTCCTGGGTTCAAG[C/T]GATTTTCCTGCCTCA	88455
rs142376760	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110013456	TCTAAGTCACTGGGC[C/T]TACCCTTTTAAGTAC	88455
rs142404727	snp	A/G	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110036136	CTGTTAGCTTTTCAC[A/G]CAGCACTATTGATAA	88455
rs142537136	snp	G/T	0.031825	0.122064	intron-variant	ANKRD13A	GRCh38.p7	12:110025271	TGAGGCACGAGAATC[G/T]CTTGAACCCAGGAGG	88455
rs142575329	snp	A/G	0.00517822	0.0506191	intron-variant	ANKRD13A	GRCh38.p7	12:110031123	AAAAAAAAAAATTAT[A/G]ATTCAGTCATCATAT	88455
rs142621358	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110027507	TTCTTACAACTGTTT[A/G]TCTAGTTTAGAGATC	88455
rs142742962	snp	C/G	0.000350079	0.0132256	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033804	TGTTTCAGCTTCCCA[C/G]ATCACAAACTTTGAG	88455
rs142776937	snp	A/G	0.00034191	0.0130705	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012116	GCAGATGTGACAAAA[A/G]AAAATCGCCAGGGAT	88455
rs142858785	in-del	-/A	0.154661	0.231107	intron-variant	ANKRD13A	GRCh38.p7	12:110001402	GTTGAGCCCTCACCG[-/A]AAGTCCAAAATTACC	88455
rs143024794	snp	C/T	0.000292224	0.0120842	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030691	GATTACATTTGGAAA[C/T]GTTAATGGCTGTAGC	88455
rs143059325	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998138	AGGCATCTGAAAGAA[C/T]GAGAAGTGCTGGAAA	88455
rs143064765	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036798	CTTCCTCTTGTGGCA[-/G]GTTACTTATAATAAC	88455
rs143224459	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004927	GCGAGCAAACTGAAG[C/T]TCAGGAGGAATTAAG	88455
rs143417220	snp	G/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110020058	GATAGTATTTGCCTA[G/T]GATGTCACATCCAGC	88455
rs143440630	snp	C/T	0.00874735	0.0655527	intron-variant	ANKRD13A	GRCh38.p7	12:110016919	CTGGGATTACAGGTG[C/T]GCGCCACTGTGCCCA	88455
rs143449160	snp	C/T	0.153997	0.230832	intron-variant	ANKRD13A	GRCh38.p7	12:110031581	GTCTGGAACTCCTGA[C/T]CTCAAGTGATCCACC	88455
rs143480702	snp	C/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110021264	TCCTTAGGATTGATA[C/T]CAGCTACGAAAAGAA	88455
rs143581063	snp	A/G	6.59163e-05	0.00574054	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033857	TTCCCGAATCTTACT[A/G]TGTTCAAGACAATGG	88455
rs143598284	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110037297	GTTAAGAAATGTAGT[C/T]ACTGCTGCCACCATG	88455
rs143644838	snp	A/G	6.59022e-05	0.00573993	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013231	GGGAGTTCCTGAGCT[A/G]CTCCAAAAAATTCTC	88455
rs143660473	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998236	ACAGAATTCCCACGC[A/G]TTCCATGGTTAGAGT	88455
rs143820322	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110034846	TTCAGATATTTGCAG[A/G]GTACCTTCTTTGTGC	88455
rs144066503	snp	A/G	0.00676609	0.0577691	intron-variant	ANKRD13A	GRCh38.p7	12:110000504	CTTTTCATTATTGCT[A/G]TCTCTTTAAAGCAGT	88455
rs144087837	snp	A/G	1.64814e-05	0.00287061	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018463	CTGGATAAGAGGGAG[A/G]CGTAGTTTTATATTT	88455
rs144203090	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110018917	TATTAAGAAAAATTC[C/T]GCACCTTTGGGGAAG	88455
rs144212333	snp	A/G	0.00121308	0.0245981	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037532	TCCAGCAAGTCTTAC[A/G]GCTGTCACTCACTGA	88455
rs144321560	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011230	TTAGCTCACACTAGA[G/T]AAATTGCTGCGTGGC	88455
rs144326895	snp	A/G	8.25484e-05	0.00642397	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110027751	AACTGTGGAACACCA[A/G]TTTGGTGCACAAGGG	88455
rs144337427	snp	A/G	0.00116931	0.0241513	intron-variant	ANKRD13A	GRCh38.p7	12:110023966	TTAAGCTGGGGGGGA[A/G]AAAAACTATAAAGGC	88455
rs144417128	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110008169	AGTTTCCTTTTATTC[C/T]TAGTATGTTGAGAGT	88455
rs144642657	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022188	GGCGTGCTGGCTCAC[A/G]CCTGTAATTCCAGCA	88455
rs144667475	snp	C/T	0.000153988	0.00877328	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037426	CTGAGCGAGACAAGC[C/T]GTTTTGATAATGACT	88455
rs144732373	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034269	TTTCTAGCACTGAAG[C/T]AGTATCATATTTTTC	88455
rs145012861	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011672	GTTGTCCGGTGATTG[C/T]ATTTCATGAAAGCTC	88455
rs145153429	snp	A/G	1.6701e-05	0.00288968	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019149	AATAGACAACTGGGC[A/G]GAGTTAATGGAAGTC	88455
rs145317403	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110008715	CATGGCAAAACCCCA[A/G]TTTTACTAAAAGTAC	88455
rs145523531	snp	C/T	0.00318978	0.0398085	intron-variant	ANKRD13A	GRCh38.p7	12:110031299	TAAAAATCAGCTTTA[C/T]TGAGGTGTAATGTAC	88455
rs145565803	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110024955	ATGCCTTTTAAATAG[C/T]GACTTGCTGGTTTTC	88455
rs145714422	snp	C/T	0.00517822	0.0506191	intron-variant	ANKRD13A	GRCh38.p7	12:110030860	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	88455
rs145843175	snp	C/T	7.13559e-05	0.00597268	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030674	CATGTCTTAAATGCA[C/T]GGATTACATTTGGAA	88455
rs145864161	snp	C/T	0.0123036	0.0774623	intron-variant	ANKRD13A	GRCh38.p7	12:110021417	TTTCTTTCTTTTCTT[C/T]TTTCTTTCTTTTTTT	88455
rs145877929	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110024519	TTGTAATCAGCAGGC[A/G]CACAGCCCATTTGCA	88455
rs145897433	snp	C/T	0.000165451	0.00909384	intron-variant	ANKRD13A	GRCh38.p7	12:110025728	CACTGTTTTCTTTCG[C/T]ATACACCTCTCAGGT	88455
rs145909252	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010765	CATGACATAGTTTTC[A/G]CAAAACAGGGAGGTT	88455
rs145984681	snp	A/G	0.0479149	0.147179	intron-variant	ANKRD13A	GRCh38.p7	12:110022238	GTGGATCACGAGGTC[A/G]GGAGATCGAGACCAT	88455
rs146028005	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110027883	AAAGGCCAAAGATAC[A/C]CCCAAGCTGGAATTT	88455
rs146349612	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:109999957	GAGTGCTTACCGTGC[A/G]ACGGGCTTTTTAAAT	88455
rs146391388	snp	C/G	0.00517822	0.0506191	intron-variant	ANKRD13A	GRCh38.p7	12:110006045	TGGTCTTGAACTCCT[C/G]ACCTCAAGTGATCAG	88455
rs146447568	snp	C/T	0.00835141	0.0640778	intron-variant	ANKRD13A	GRCh38.p7	12:110036431	CCTCAGGCAGATGTA[C/T]GGTGCCACAAACTGG	88455
rs146603421	snp	C/T	4.94499e-05	0.00497217	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028520	TCAGCAGGACCTCAC[C/T]ACGGAATGTGCTACT	88455
rs146820666	snp	A/G	0.000132371	0.00813438	intron-variant	ANKRD13A	GRCh38.p7	12:110018514	TCTCTTGTAGTAATC[A/G]CTGCTCAAGCAAAAT	88455
rs146974610	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997787	GTTTTTCTTCATATG[C/T]GTGGAATTTGAGAAT	88455
rs146984356	snp	A/G	0.00636936	0.0560724	intron-variant	ANKRD13A	GRCh38.p7	12:110003887	TTTTTGGCTGGGCAC[A/G]GTGGCTCACGCCTGT	88455
rs147223311	snp	C/T	0.0232847	0.105357	intron-variant	ANKRD13A	GRCh38.p7	12:110012227	AAAATTAGCCAGGTG[C/T]GGTGGTGCATGTCTG	88455
rs147330673	snp	C/T	0.0158469	0.0875917	intron-variant	ANKRD13A	GRCh38.p7	12:110034903	TCTCTGGGAAGCAGC[C/T]CCTGCCCTCACAGGG	88455
rs147375947	snp	C/T	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110011623	TTCTAGACTTGAATG[C/T]TGATATGTGCTTGAG	88455
rs147398713	snp	A/T	0.000345984	0.0131481	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013166	GATCCTGAGATGGTG[A/T]ACACAGTTCTCCAAC	88455
rs147635905	snp	A/G	0.115088	0.210473	intron-variant	ANKRD13A	GRCh38.p7	12:110008783	CCAGCTACTCAGGAG[A/G]CTGAGGCACAAGAAT	88455
rs147740459	snp	C/T	0.046775	0.145601	intron-variant	ANKRD13A	GRCh38.p7	12:110030927	TGGAGAAACCCTGTC[C/T]CTACTAATAATACAA	88455
rs148046644	snp	G/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038128	CCACACCCAGCTAAA[G/T]TTAGAGGAGATACAT	88455
rs148099833	snp	G/T	0.0023933	0.0345097	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998280	CCTGGTGCTCCTGCA[G/T]CCTGTTTTGGTTTAA	88455
rs148216597	snp	A/G	0.0205511	0.0992634	intron-variant	ANKRD13A	GRCh38.p7	12:110026610	TTCCTGGCTGAGCAC[A/G]GTGGCTCACACCTGT	88455
rs148221071	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110011300	TGGCAGAATAGGAAC[A/G]AAGAGGTAAGAGCCA	88455
rs148472356	snp	C/T	0.0209421	0.100162	intron-variant	ANKRD13A	GRCh38.p7	12:110022199	TCACGCCTGTAATTC[C/T]AGCACTTTGGGAGGC	88455
rs148474691	in-del	-/A	0.0267878	0.112589	downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039727	ACATCAAAGCTCTGC[-/A]ATCAATGCTATCCCT	88455
rs148691609	snp	C/T	0.000725318	0.0190298	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018474	GGAGGCGTAGTTTTA[C/T]ATTTAAGGGAGAAGG	88455
rs148736556	snp	A/G	0.0103295	0.0711199	intron-variant	ANKRD13A	GRCh38.p7	12:110028979	CTGACCTTGTGATCC[A/G]CCCGCCTGGGCCTCC	88455
rs148892794	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110037037	AGATTACGGGAAAAA[C/T]CGCGAGGATTCATTT	88455
rs149017101	snp	A/G	0.000106718	0.00730394	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030675	ATGTCTTAAATGCAC[A/G]GATTACATTTGGAAA	88455
rs149135826	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110019401	CATGTATGTATTAAT[A/T]GTAAATTATGGATGG	88455
rs149336715	snp	C/T	1.65165e-05	0.00287367	synonymous-codon, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037401	CACAGAAGGCCTGTG[C/T]CCCAGCGCCCTGAGC	88455
rs149388161	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034120	GGTCTTCTTACAAAA[A/G]CTTGTTATGTAAGAG	88455
rs149402787	snp	A/G	0.00597247	0.0543191	intron-variant	ANKRD13A	GRCh38.p7	12:110016626	GGGTGTTTTTCATCC[A/G]GTCTTCCCCGCCATG	88455
rs149618093	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011227	GACTTAGCTCACACT[A/G]GAGAAATTGCTGCGT	88455
rs149672222	snp	C/T	0.00835141	0.0640778	intron-variant	ANKRD13A	GRCh38.p7	12:110007537	AGACATGTGCCACCA[C/T]GCCCGGCTAATTTTG	88455
rs149720161	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012602	CCATACACGAATGTG[G/T]AGGCCAGTTTTCCCC	88455
rs149763123	snp	A/C/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110024305	GGGATAGCATGCCCT[A/C/G]AGGAGGTCTGTAGCT	88455
rs149815364	snp	C/T	0.0142736	0.0832652	intron-variant	ANKRD13A	GRCh38.p7	12:110031262	ATATGATCCTAGTTA[C/T]ATTAAAAAGAAAGGA	88455
rs149916969	snp	A/G	4.94197e-05	0.00497066	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110036315	ACAAACACCTATGAC[A/G]CCCAGTATGAGAGGT	88455
rs150196287	snp	A/G	0.00478085	0.0486577	intron-variant	ANKRD13A	GRCh38.p7	12:110009896	TTGAGACGGAGTCTC[A/G]CTCTGTCACCCAGGC	88455
rs150245310	snp	A/G	0.000691654	0.0185836	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028576	CTGATGAGTACTTCA[A/G]TGAAGAGTTTGATCT	88455
rs150289231	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110027283	GATTAGATGAGTTAC[A/G]ACGTGGAAGCCTTTA	88455
rs150439214	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038447	GGTGTGTTCTACACC[C/T]GCATGAGTGAAGGAT	88455
rs150544403	snp	C/T	0.0599851	0.162463	intron-variant	ANKRD13A	GRCh38.p7	12:110006745	GGGATTACAGGCATG[C/T]GCCACCATGCCTGGC	88455
rs150701920	snp	C/T	0.00795532	0.062565	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998936	GAGGTTGAGAAATCA[C/T]GAAGTAGAAATATCC	88455
rs150759668	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110033617	AAATCAAGGAAAAAG[A/G]AAAAAGCTGTATTCT	88455
rs150797695	snp	C/T	0.0256215	0.110247	intron-variant	ANKRD13A	GRCh38.p7	12:110017761	AACATGGTGAAACCC[C/T]GTCTCTACAAAAATA	88455
rs150813879	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110030414	TCAGGTGATCAGCTC[A/G]CCTTGGCCTCCCAAA	88455
rs151069038	snp	C/T	0.00318978	0.0398085	intron-variant	ANKRD13A	GRCh38.p7	12:110009444	TCCATCTTTAATTCC[C/T]GATTTTAGTAAGTTA	88455
rs151225356	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001772	TTTGTGAGAGTCATC[A/G]TTCTTAATTAGATGA	88455
rs151259039	snp	A/G	0.000198331	0.00995621	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110024092	GATAAAGCAGAAGTT[A/G]TTAATGGTTACGAAG	88455
rs151289036	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110036158	TATTGATAATGGTCA[C/T]GGAAAGACTTTTAAT	88455
rs151320122	snp	G/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110020110	TAGCCTGAGAAAATG[G/T]ACACTATCATCCTGA	88455
rs180711712	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016662	GACTTTTCCTCCCAG[G/T]CATTCATGAAGGTAG	88455
rs180896876	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011610	CCTATACTTCCTATT[C/G]TAGACTTGAATGCTG	88455
rs180911068	snp	C/G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036635	CAGGCACCTGTAGTC[C/G/T]CAGCTACTCGGGAGG	88455
rs180953106	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110000460	TCCTTAAAATCCCTT[C/T]CTGTTCTAAAGTGCT	88455
rs181109768	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015721	CGAGCTAATTTTTGT[A/G]TTTATAGTGGAGATG	88455
rs181116413	snp	G/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110007370	CTTCTTTAATTTTTT[G/T]AGGTTTTTTTTGTTT	88455
rs181254797	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110028840	CCTCCCAGGTTCAAG[C/T]GGTTCTCCTGCCTCA	88455
rs181330010	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011299	GTGGCAGAATAGGAA[C/T]GAAGAGGTAAGAGCC	88455
rs181508249	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022999	CTAATTTCATTGACC[A/T]AATCCCATTAGAAGA	88455
rs181631900	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110036037	CTGATTTTGTACAAA[A/G]GATGAGAAGGTTGTG	88455
rs181639760	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001716	TGAGCCACTGTTGCC[A/G]GCCTTTTTTCATTTA	88455
rs181651924	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110017124	TATGTTGGCCAGGCT[A/G]GTCTCGAACTCCTGT	88455
rs181816712	snp	A/C	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110006072	TCAGCCCACCTTGGC[A/C]TCCCAAAGTTCTGGG	88455
rs181869984	snp	C/T	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110022321	AGACGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	88455
rs182034791	snp	A/C/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110027885	AGGCCAAAGATACCC[A/C/G]CAAGCTGGAATTTGA	88455
rs182049873	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007791	TTTGATGCTATTATA[A/G]ATGGAATTGTTGTCT	88455
rs182050000	snp	A/G	0.00123931	0.024862	intron-variant	ANKRD13A	GRCh38.p7	12:110029648	TAGGTACTGCTAAAT[A/G]AACTTCAGCAACACT	88455
rs182374721	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110012565	CTCATCCAGAAACAG[C/T]TCTCAGTGCAAACTT	88455
rs182387760	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038450	GTGTTCTACACCTGC[A/C]TGAGTGAAGGATTTC	88455
rs182419982	snp	C/T	0.00636936	0.0560724	intron-variant	ANKRD13A	GRCh38.p7	12:110013791	CAAGACCTAAAATAA[C/T]AATAAATATAATAAT	88455
rs182449540	snp	G/T	3.29881e-05	0.00406115	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018478	GCGTAGTTTTATATT[G/T]AAGGGAGAAGGTGAG	88455
rs182632750	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997431	GAATATATTAGATGA[A/T]TCCTTAGGCTTCAGT	88455
rs182633257	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002445	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	88455
rs182639541	snp	A/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110009114	GAGACGAAGTTTTAC[A/T]CTTGTTGCCCAGGCT	88455
rs182656767	snp	C/T	0.00517822	0.0506191	intron-variant	ANKRD13A	GRCh38.p7	12:110032093	GGACATCTAGTACAA[C/T]GTTGAGTAAGAGTGG	88455
rs182870560	snp	C/T	6.60644e-05	0.00574698	intron-variant	ANKRD13A	GRCh38.p7	12:110013292	AATCTGAGCTAAATG[C/T]TGATACAATTACTGG	88455
rs182870754	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038035	GGTAATCTGTGCTGA[C/T]CTCCTTATTTTTACC	88455
rs182976848	snp	A/G	0.00517822	0.0506191	intron-variant	ANKRD13A	GRCh38.p7	12:110024720	TCTGAGTGAGCAAAG[A/G]AAGGCTTACGTCATG	88455
rs183149945	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110036802	CCTCTTGTGGCAGTT[A/T]CTTATAATAACTCTA	88455
rs183202634	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110025701	TACTTTTGGAGTTTT[A/G]ATTCCCTGTGTCACT	88455
rs183230470	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110002723	CAGTTTCCTCATTCC[A/G]TCTATCACCTGATTG	88455
rs183322483	snp	A/G	0.021333	0.101051	intron-variant	ANKRD13A	GRCh38.p7	12:110026255	CAGGCGTGAGCCACC[A/G]TGCCTGGCCCCTAAC	88455
rs183555210	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110003591	CAGCAGCCTCTTGCT[A/G]GAGTCCCCCTAAAGG	88455
rs183565372	snp	A/G	0.00478085	0.0486577	intron-variant	ANKRD13A	GRCh38.p7	12:110008340	TCTTATATTTGTAGG[A/G]TAAGTCTCAGTTGGT	88455
rs183651638	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001133	AAGCTAACAAACTTA[G/T]CAGTTAGGATGAGGA	88455
rs183656351	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032942	TCCAGAGAAGAGCTA[A/G]GCAGTGTAAACAACT	88455
rs183691643	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110009499	CTATCTAACTAAATG[G/T]TCGTCAATGTTGTTG	88455
rs183803509	snp	A/C	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110030455	TACAGGTGTAAGCCA[A/C]CGCGCCTGACCGAAA	88455
rs183887933	snp	C/T	0.00874735	0.0655527	intron-variant	ANKRD13A	GRCh38.p7	12:110004236	AATAGGAAGGAAACT[C/T]CTAGTTAAAGGAGGA	88455
rs183992793	snp	C/T	1.64741e-05	0.00286998	missense, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110036321	ACCTATGACGCCCAG[C/T]ATGAGAGGTGATTGA	88455
rs184169877	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022196	GGCTCACGCCTGTAA[C/T]TCCAGCACTTTGGGA	88455
rs184217459	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110015398	TTCCCTGCCCTTTGC[C/T]TAGAATAGGTGGTTA	88455
rs184422440	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020208	CGCTATTATCCTTAT[A/G]GTATTTGTCTAGAAT	88455
rs184462297	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998661	AAATCCAAAAAGCTA[A/G]CTTAAAAATGACATT	88455
rs184534904	snp	A/G	0.00318978	0.0398085	intron-variant	ANKRD13A	GRCh38.p7	12:110015767	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTTAA	88455
rs184592554	snp	C/T	0.0182019	0.0936463	intron-variant	ANKRD13A	GRCh38.p7	12:110026363	CGAGTCACCTGAGGT[C/T]GGGAATTCAAGACCA	88455
rs184804354	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110000184	CTCAAAGACGTAAGA[A/G]TAGCACACTCTCCTT	88455
rs184916771	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020862	TTTCCTTAGCTGAAA[G/T]AAATAATTGAGTGAA	88455
rs184958935	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110026796	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCCAGAG	88455
rs184958983	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005420	ACAGGTGTTAGCCAC[C/T]GCACCCACCCTGTAA	88455
rs184983464	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110024804	AGCTTTGAATGTTGG[G/T]GCTCCTCACGTGGCA	88455
rs185020672	snp	A/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110002578	CCAAGATCGTGCCAC[A/T]GCACTCCAGGCTGGG	88455
rs185022734	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110036791	CTCTCTTGCTTCCTC[C/T]TGTGGCAGTTACTTA	88455
rs185229729	snp	A/G	0.00914312	0.0669923	intron-variant	ANKRD13A	GRCh38.p7	12:110028927	ATTTTTAGTAGAGAT[A/G]GGGTTTCACCATATT	88455
rs185261351	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007374	TTTAATTTTTTGAGG[G/T]TTTTTTTGTTTGTTT	88455
rs185283895	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010873	AGACTGCAGGGGTAG[A/T]TAGTACCTGAATAAC	88455
rs185462067	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034223	CGCACATAGCTTGTA[A/G]TTCTGTACTTTTTGA	88455
rs185589885	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038880	TCCCACAGGCTGCAC[C/T]GAAATAACCTGGTAA	88455
rs186022317	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110011852	ATTCATATTTTAACT[A/G]TGCCCAAATGCAAAC	88455
rs186032978	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110017824	GTAATCCCAGCTACT[C/T]GGGAAGCTAAGGCAG	88455
rs186267880	snp	A/G	0.00318978	0.0398085	intron-variant	ANKRD13A	GRCh38.p7	12:110001526	GTCACTGCAACCTTC[A/G]CCTCCCGGGTTCCAG	88455
rs186284483	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110022522	GAGCAGAGGTAGCCC[A/G]GTGAGGAGCTTGGTG	88455
rs186353568	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007906	ACTCATTTAATAGTT[C/G]TAATAGTTTTTTGGT	88455
rs186362260	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110030016	GTAAATATGATCTAC[A/G]TCCCAAGCTAGTATG	88455
rs186369744	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001899	TTTCTATTACTAGAC[A/G]TGGTACAGAGGTAAA	88455
rs186567971	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033055	TGTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	88455
rs186647404	snp	A/G	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110023673	AGTTAAGATGACCCA[A/G]ATAAATGCTCTGACC	88455
rs186679330	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110028711	TGTTTTATGGTGTTA[C/T]GTTGGATCATTCCAC	88455
rs186933572	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110012779	GACTGAGCAGGGATA[C/T]TGTAGGCCAAGCCCT	88455
rs187024491	snp	C/T	0.0142736	0.0832652	intron-variant	ANKRD13A	GRCh38.p7	12:110009150	GCAATGGCACAATCT[C/T]GGCTCACCACAACCT	88455
rs187024685	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032755	CAACAGAATAACATA[C/T]AGTATTGAAAATAAA	88455
rs187149341	snp	C/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037773	TGCAGGCCCCATCTC[C/T]AGGCTAAGGGGAGGA	88455
rs187256320	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038306	GCAATTCTTTTGAGA[A/G]CAGGATTCTCCAGGC	88455
rs187259001	snp	C/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110013459	AAGTCACTGGGCTTA[C/T]CCTTTTAAGTACTAT	88455
rs187299153	snp	C/T	0.00636936	0.0560724	upstream-variant-2KB, utr-variant-5-prime	ANKRD13A	GRCh38.p7	12:109999239	GGTAGACGGAACTTT[C/T]CGCGTGGAGATCTTT	88455
rs187355681	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020432	TCTAATTTAGATTGA[A/G]CTGTGGAATTAGGAC	88455
rs187412385	snp	C/T	0.00636936	0.0560724	intron-variant	ANKRD13A	GRCh38.p7	12:110016682	CATGAAGGTAGTATA[C/T]AGACAATTTCATTTC	88455
rs187562701	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110003138	GAGACATGAACACTT[A/G]AGGGGACAGATGCAA	88455
rs187564276	snp	A/G	1.65482e-05	0.00287643	intron-variant	ANKRD13A	GRCh38.p7	12:110025727	TCACTGTTTTCTTTC[A/G]CATACACCTCTCAGG	88455
rs187578400	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038693	TAAAAACAACTCCCA[C/T]CAGTAGCAATACAAG	88455
rs187752640	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110018074	TATATAGTGGGGACA[A/G]ACCCCACTATAAATT	88455
rs187842776	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997463	TTAATCTCATGTTCA[A/G]AATTAAGATAATGCA	88455
rs188041102	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110004001	ATCTTTGCTAAAAAT[A/G]TGAAAAATTAGCTGG	88455
rs188267044	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110004790	ACTACATAGTGTGGG[C/T]GTATGATAATAACAG	88455
rs188284922	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110026650	ACTTTGGGAGGCCAA[A/G]GTGGGCAGATCACTT	88455
rs188326865	snp	C/G	0.046775	0.145601	intron-variant	ANKRD13A	GRCh38.p7	12:110026321	GCTCATGCTTGTAAT[C/G]CCAACACTTTGGGAG	88455
rs188430414	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110036487	AGGAGCGGTGGCTCA[C/T]GCCTATAATCCCAGC	88455
rs188547399	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110029169	CTTTTTTTTTTTATT[G/T]CTAACCAGCTTCAGC	88455
rs188564695	snp	A/G	0.00874735	0.0655527	intron-variant	ANKRD13A	GRCh38.p7	12:110008559	AAAAGTTTGTGAAAC[A/G]TTGGTATTAATTCTT	88455
rs188583359	snp	A/G/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110015076	CCAGTGCGCCCGGCC[A/G/T]CATTTCTCTTCTTGA	88455
rs188680364	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015439	CTTGGCAGTGCTTAA[A/G]CCCATCTTCCCAGGT	88455
rs188868170	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039152	TTTGTTTGTTTCAAA[C/T]ATGCAGTGTGGTATT	88455
rs189043319	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110022564	GAAAAGCATAGCGCC[A/G]TCTTCCCAGCGTGCA	88455
rs189184677	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033447	TTAAGTGTTCAGATA[C/T]TTTATATATACTTTT	88455
rs189288875	snp	G/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110026950	GTTTCCCCATAGTTG[G/T]CCTCAGCTGTAATTA	88455
rs189390142	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110021071	TATTCCATTTGTACC[A/G]AGGACTAAGGCACAT	88455
rs189415150	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015772	GGCTGGTCTCGAACT[C/G]CTGACCTTAACTCAT	88455
rs189589066	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001177	CTGAAATCTAGTATG[A/G]TTGTTCTTGTTGACT	88455
rs189601741	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022245	ACGAGGTCGGGAGAT[C/T]GAGACCATCCTGGCT	88455
rs189665315	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110000246	TCCAGGTTCTAACTC[G/T]CCCTGTGACCTTGGG	88455
rs189732163	snp	G/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110007018	GACCATAAATGTGTG[G/T]GTTTATTTCTGGACT	88455
rs189743845	snp	A/C	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110007506	CTGCCTCAGCCTCCC[A/C]AGTAGCTGGGATTAC	88455
rs189748288	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110029312	ATTTTAGGGTGATGT[A/G]AATTCCTTGTGGCCC	88455
rs189946767	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110034952	TGCTCACACTCCAGC[A/G]TCCTCACTGGTTCAA	88455
rs189947492	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110028793	CCTAGGCTGGAGTGC[A/G]GTGGCACGAACTCGG	88455
rs189955315	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110001663	GGCCTCAAGCAATCC[A/G]CCCACCTCTACCTCC	88455
rs190120075	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110013779	TGGGTGACAGAGCAA[A/G]ACCTAAAATAATAAT	88455
rs190178329	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038411	GCTGGCCAAAATATT[A/G]GAACACACAGAACCA	88455
rs190232696	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110011146	TTTCCAAAAGTCCAT[A/G]GCAGTTTGTTGTATT	88455
rs190367799	snp	A/C	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110017904	GCCACTGCACTCCAG[A/C]CTGGGCGACAGGGTG	88455
rs190456084	snp	C/T	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110005818	TTTGTGTATATGTTT[C/T]TGTGGGTTTCCTTTT	88455
rs190462550	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110010119	TGATCCACCCACCTC[A/G]GCCTCCCGAAGTGCT	88455
rs190681274	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110012876	AAACACATTATCAGG[A/G]TTTCGCAACCAGTGG	88455
rs190828512	snp	A/C/G	0.00119737	0.0244387	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997336	GTGAGCAGAGATCGC[A/C/G]TCACTGCACTCCAGC	88455
rs190924655	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110016921	GGGATTACAGGTGCG[C/T]GCCACTGTGCCCAGC	88455
rs191001980	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002668	AGCAATAAAGTGGCT[G/T]TTTCCCTTAATGTTT	88455
rs191034634	snp	G/T	0.0209421	0.100162	intron-variant	ANKRD13A	GRCh38.p7	12:110024661	CAACAGGGATTGATG[G/T]CTTTTGGTGTTGGAG	88455
rs191072410	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110018223	AAAGCCAAGAAGTCC[A/G]TTGTTTGATGGTCAC	88455
rs191073684	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110025398	CAGAAGTACAGGATC[A/C]TGGTTTGGGTACCTT	88455
rs191449539	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110009474	AAGTCTTCTCTCTTT[C/T]TTCCCTGGTCTATCT	88455
rs191631032	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037979	GTAAAGTGTGATCTA[C/T]GAGAATTGGAGACAC	88455
rs191846889	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020810	CTCCTAAATAACTGC[A/G]ACTTTGGGCAAGTGG	88455
rs191849125	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110030198	TTGAGATGGAGTCTC[A/G]CTCTGTTGCCCAGGC	88455
rs192045554	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110012535	AGGCCAGAAACCCTC[A/G]GTAGAGAATGACTCC	88455
rs192148728	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110008047	TTGACTAGATATGGT[A/G]AAAGAGGACATCCTC	88455
rs192180192	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015184	TGTGGTAGTTTAAAA[C/T]TTCAGAAAGCCAAAT	88455
rs192182399	snp	A/G	0.00318978	0.0398085	downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039502	CACACTTCCTGTTAC[A/G]TATGTCAGTAGAACA	88455
rs192362157	snp	G/T	0.00795532	0.062565	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997995	AGCCAGGTACTATTT[G/T]GGTTTTAGATACTCT	88455
rs192416870	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110037038	GATTACGGGAAAAAC[C/T]GCGAGGATTCATTTT	88455
rs192421889	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020207	ACGCTATTATCCTTA[C/T]AGTATTTGTCTAGAA	88455
rs192659203	snp	A/C	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110026322	CTCATGCTTGTAATC[A/C]CAACACTTTGGGAGG	88455
rs192667323	snp	C/T	0.00318978	0.0398085	intron-variant	ANKRD13A	GRCh38.p7	12:110004842	TGTGGTGTCAAGCAC[C/T]GTGCTAAGTTAAGGA	88455
rs192670046	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110026750	AACCAGGCGTGGTGG[C/T]GCACTCCTGTAGTCT	88455
rs192761321	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110022118	AAATTTAAAACAGGG[C/T]ATGAACATTGGGTTG	88455
rs192794188	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110008605	ATTCACCAGTGAAGT[C/T]CAGGCATGGTGGCTC	88455
rs192877198	snp	A/G	0.00478085	0.0486577	intron-variant	ANKRD13A	GRCh38.p7	12:110004229	ATGAGCAAATAGGAA[A/G]GAAACTCCTAGTTAA	88455
rs192907389	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110003433	TGCCCCCTTGGTCAT[C/T]GGGGGTTCAAGCTCA	88455
rs192990670	snp	G/T	0.00356974	0.0420966	intron-variant	ANKRD13A	GRCh38.p7	12:109999816	GGGTCCGTCTCCCGG[G/T]GGGGACTTCGGGGAA	88455
rs193011043	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110031954	CTTGTCTTACACTTT[C/T]TTGTAGATTTCTTAG	88455
rs193150426	snp	A/G	0.0228947	0.104514	intron-variant	ANKRD13A	GRCh38.p7	12:110014209	CGAGGTCAGGAGACC[A/G]AGACCATCCTGACTA	88455
rs193156190	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110026042	CCTTGGCTCACTGCA[A/G]CCTCTGCCTCCTGGG	88455
rs193238443	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010302	ATGCTAAACCTAGCA[C/T]CTTTCATTTAGATTG	88455
rs193290900	snp	C/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038715	CAATACAAGGTTATA[C/T]ATTTTAACCAGATTT	88455
rs199565526	snp	A/C/G/T	0.00446732	0.0470523	missense, synonymous-codon, utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037416	CCCCAGCGCCCTGAG[A/C/G/T]GAGACAAGCCGTTTT	88455
rs199636259	snp	A/G	3.33367e-05	0.00408255	intron-variant	ANKRD13A	GRCh38.p7	12:110024004	ATAAATCTGAATGGC[A/G]TATTGTACATGTAGA	88455
rs199700471	snp	C/T	1.64803e-05	0.00287052	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033852	TGAAATTCCCGAATC[C/T]TACTATGTTCAAGAC	88455
rs199876238	snp	C/T	3.39616e-05	0.00412064	intron-variant	ANKRD13A	GRCh38.p7	12:110033778	AACTCAGACACTGGA[C/T]GGTTGCCTTTTGTTT	88455
rs199998919	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110035442	GATCCTATATCTACC[-/A]AAATTTTTTTTTTTT	88455
rs200035769	snp	A/T	0.152334	0.230133	intron-variant	ANKRD13A	GRCh38.p7	12:110035447	CTATATCTACCAAAT[A/T]TTTTTTTTTTTTTAA	88455
rs200055440	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110017946	CAAAAAAAAAAAAAA[-/G]TGGCATACTTTAGAC	88455
rs200084695	snp	C/T			synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030721	CACTGCCGAAGAATC[C/T]GTATCTCAAAATGTG	88455
rs200295454	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110011108	AGACCTTGTTTAAAA[A/G]AAAAAAAAAAAAAAG	88455
rs200379593	snp	C/G	0.000404831	0.0142215	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999755	TGGAAAAACGACTAC[C/G]GGCAGCTCGAGAAGG	88455
rs200391814	in-del	-/TC			intron-variant	ANKRD13A	GRCh38.p7	12:110025951	CTAACCCTAACTTCT[-/TC]TCTCTCTCTCTCTTT	88455
rs200404733	in-del	-/C			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997714	CTGGATAGTAACCCC[-/C]TCAGTAAATAGTAGC	88455
rs200429928	snp	A/G	0.000298231	0.0122076	intron-variant	ANKRD13A	GRCh38.p7	12:110013116	AAATTTCACCCTTTT[A/G]TTTTCTAGTTTTACA	88455
rs200740786	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110014961	CTAATTTTTTTTTTT[-/T]GTATTTTTAGTAGAG	88455
rs200762511	snp	A/G	0.000115723	0.00760578	intron-variant	ANKRD13A	GRCh38.p7	12:110011984	CATCCAATTATGTAA[A/G]TGCCAGTGTTTCCTT	88455
rs200823148	snp	C/G	0.000264432	0.0114955	intron-variant	ANKRD13A	GRCh38.p7	12:110013298	AGCTAAATGCTGATA[C/G]AATTACTGGAGACAC	88455
rs200987985	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110037335	TAGTAGTGACTCTCC[C/G]TTTTTATCTGTTTTC	88455
rs201033734	snp	A/T	0.0271762	0.113356	intron-variant	ANKRD13A	GRCh38.p7	12:110035460	ATTTTTTTTTTTTTT[A/T]AATTTTTGAGGCAGA	88455
rs201128516	in-del	-/AAAG			intron-variant	ANKRD13A	GRCh38.p7	12:110022463	CAAAAAAAAAAAAAA[-/AAAG]AGTGCAAATGCTTAG	88455
rs201199377	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033747	TTTTGCAAAAAGTTG[A/G]AGTGGAAATGTAATG	88455
rs201257737	in-del	-/A	0.0119091	0.0762411	intron-variant	ANKRD13A	GRCh38.p7	12:110001073	AGAAACTCTGCTTTT[-/A]AAGTCTCCCAACAAT	88455
rs201493633	in-del	-/TTTTT	0.0263992	0.111815	intron-variant	ANKRD13A	GRCh38.p7	12:110008982	CAGATTTTTGGTTTC[-/TTTTT]GAGTCAGTTTTGCTA	88455
rs201518434	snp	G/T	1.65258e-05	0.00287448	intron-variant	ANKRD13A	GRCh38.p7	12:110024025	TACATGTAGAAATTT[G/T]TGGTGTTCACTTTTT	88455
rs201635003	in-del	-/CATCCCAGCCC	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110027146	TGCATGTGGTTGCCA[-/CATCCCAGCCC]CATCCCAGCCCCACC	88455
rs201713968	snp	C/G	3.35649e-05	0.0040965	intron-variant	ANKRD13A	GRCh38.p7	12:110013082	CTGGTTTTGGAATTT[C/G]TCAGAAAGTATGAGA	88455
rs201753905	in-del	-/CAGGGAG			intron-variant	ANKRD13A	GRCh38.p7	12:110020674	ATACCCTTCTGCAGA[-/CAGGGAG]GCCCCTTCAGCTTAG	88455
rs201846270	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110006613	TGTCTTTTTTTTTTT[-/T]GAGATGGAGTTTCGC	88455
rs201849646	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110035446	CCTATATCTACCAAA[A/T]TTTTTTTTTTTTTTA	88455
rs201912040	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110033304	CCTGACCTTGTGATC[A/T]GCCTGCCTCAGCCTC	88455
rs202016663	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110009660	ACAGCATTTTTTTTC[G/T]ACTGCCTCTTCAGAT	88455
rs202049339	snp	C/G/T	0.000119927	0.00774279	intron-variant	ANKRD13A	GRCh38.p7	12:110012168	CAATAATTTAAAGTC[C/G/T]GTCTGAGCACCATGG	88455
rs202120045	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110035462	TTTTTTTTTTTTTTA[A/T]TTTTTGAGGCAGAGT	88455
rs367616134	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110001369	AGCTGTGTGCTTGCA[A/C]CCTGCCATATTTAAG	88455
rs367685556	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110030846	ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG	88455
rs367703492	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029564	ACCTAATGGCTCGAA[C/T]GAGTGCTCATTTTGC	88455
rs367742868	snp	C/G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036396	ACAGGCGAGCAGACG[C/G/T]GTGGCACTGTGCATT	88455
rs367745440	snp	A/G	4.96249e-05	0.00498096	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019169	TAATGGAAGTCAACC[A/G]TGATGACAAAGTGGT	88455
rs367868998	snp	C/G	0.000117579	0.00766653	intron-variant	ANKRD13A	GRCh38.p7	12:110013075	TTTCAGCCTGGTTTT[C/G]GAATTTGTCAGAAAG	88455
rs367870655	snp	A/G	0.000148722	0.00862201	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012081	ATTTGGAATCTGCTC[A/G]AGTCTTACTCCGACA	88455
rs367914311	snp	A/G	4.94254e-05	0.00497094	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028616	GGACATTGGAAGGCC[A/G]AAAGAGCTGACGATT	88455
rs368090099	snp	G/T	0.000871679	0.0208586	intron-variant	ANKRD13A	GRCh38.p7	12:110019372	TCTAATCCCCATGCT[G/T]CCATCTTGAGTGACA	88455
rs368097749	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110022584	CCCAGCGTGCATGAA[A/G]GGTGAGGTGGAGCAG	88455
rs368237200	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110012616	GGAGGCCAGTTTTCC[C/G]CTGAGGAATATGGTT	88455
rs368273015	snp	A/G	3.49748e-05	0.00418165	intron-variant	ANKRD13A	GRCh38.p7	12:110019093	CTTCCTTGTTTTTGC[A/G]TCTTCCCTACTTTGC	88455
rs368306678	in-del	-/C	0.0100269	0.0700921	intron-variant	ANKRD13A	GRCh38.p7	12:110028684	AACCTATGTATGTTT[-/C]AGAAATTGTGCTGTT	88455
rs368322106	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110024644	CTTTCAGTCCCTCAG[C/T]ACAACAGGGATTGAT	88455
rs368389044	snp	C/T	1.72077e-05	0.00293318	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030708	TTAATGGCTGTAGCA[C/T]TGCCGAAGAATCTGT	88455
rs368511846	snp	A/T	0.000153988	0.00877328	stop-gained, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019243	ACTCTGGACTTGATG[A/T]AGCCAAAAAGCAGGG	88455
rs368521635	snp	C/T	0.000153988	0.00877328	intron-variant	ANKRD13A	GRCh38.p7	12:110012002	CCAGTGTTTCCTTCA[C/T]AGAATGTGGAGGCTG	88455
rs368786132	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110004038	TGGCGGGTGCTTGTA[A/T]TCCCAGCTACTTGGG	88455
rs368859405	snp	C/T	0.00318978	0.0398085	intron-variant	ANKRD13A	GRCh38.p7	12:110032777	GAAAATAAAAATTTA[C/T]AGCTATGTGCGTCAA	88455
rs368898054	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110033055	TGTTTTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT	88455
rs368972163	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110020754	TGCCACTGTTCATCC[A/G]TAGGGATGAGATGGG	88455
rs368980091	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110018809	AAATGGCATTGCTCA[C/T]CCAATGTTGTGCATA	88455
rs369004766	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110016182	TCAAACTCCTGAGCG[C/T]AAGTGATCACCCGCC	88455
rs369158995	snp	C/T	1.71661e-05	0.00292963	intron-variant	ANKRD13A	GRCh38.p7	12:110024145	AAATAAGATTTAATA[C/T]AGCTATTTAGCTTCT	88455
rs369198395	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	ANKRD13A	GRCh38.p7	12:109999210	CTGGAGCAGGGGGAA[A/G]GAAGCTGGGGACAGG	88455
rs369335618	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110009308	CTGGTCTCGAACTCC[C/T]GACCTCTAGTGATCC	88455
rs369353301	snp	C/T	1.64781e-05	0.00287033	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110016415	TATGTGCAGATGAAA[C/T]GGGAATTCACCAGCT	88455
rs369356517	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110014095	ATTAATAGCTCTATC[A/G]AGAAAAGGAACAACT	88455
rs369381433	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:109999908	CCCTTCCACTTTGCA[A/G]GTGTGGGACAGTCCT	88455
rs369382030	in-del	-/TG			intron-variant	ANKRD13A	GRCh38.p7	12:110034459	GTAAGCAGTAGGCTT[-/TG]TGTGTGTGTGTGTGT	88455
rs369473960	snp	A/G	3.35182e-05	0.00409365	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019313	GCCTCGATACTAAAA[A/G]TATTGCTTTTGAAAG	88455
rs369606770	snp	A/G	0.000346366	0.0131553	intron-variant	ANKRD13A	GRCh38.p7	12:110013272	TGAAAATGTGGCCAG[A/G]CCATAATCTGAGCTA	88455
rs369648624	snp	C/T			intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034168	AGTCAGCACCATTCA[C/T]AAGATGTCTTCAGGC	88455
rs369663397	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110004581	GATCTCGGTGAGCTA[A/T]GATTGCACCATTGCA	88455
rs369794302	snp	A/G	1.78258e-05	0.00298539	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033985	GAATACTCTAATGGC[A/G]GGGCGTGGGAGGTCT	88455
rs370014794	snp	A/G	0.0271762	0.113356	intron-variant	ANKRD13A	GRCh38.p7	12:110035597	TGGGATTACAGGTGC[A/G]CACCACCAGACCCAG	88455
rs370016597	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036477	AAAGTAGGCCAGGAG[C/T]GGTGGCTCACGCCTA	88455
rs370048110	snp	A/G	1.64738e-05	0.00286995	intron-variant	ANKRD13A	GRCh38.p7	12:110036369	TAAACCAGGGTGAAC[A/G]CAGGCCTGGACACAG	88455
rs370163748	snp	A/G	0.00113607	0.0238064	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018396	GTCGCATCTGGAAAA[A/G]TGGTGCCAAACTGCG	88455
rs370211635	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110002669	GCAATAAAGTGGCTG[G/T]TTCCCTTAATGTTTT	88455
rs370384203	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110007701	TCTTTAATTTTTTTT[A/G]AACAATGTTTTATGG	88455
rs370433255	snp	A/G	4.94466e-05	0.00497201	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028639	TGACGATTAGAACAC[A/G]GAAGTAAGAGAGGTT	88455
rs370580517	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110030884	TGGATCACCTGAGGT[C/T]GGGAGTTTGAGACCA	88455
rs370583047	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002252	CATTTGTAAACCTGG[A/G]GATTGAGCTTTTTTG	88455
rs370650390	snp	A/G	0.000131781	0.00811621	missense, synonymous-codon	ANKRD13A	GRCh38.p7	12:110036310	GCCAGACAAACACCT[A/G]TGACGCCCAGTATGA	88455
rs370743235	snp	A/G	1.73909e-05	0.00294875	intron-variant	ANKRD13A	GRCh38.p7	12:110019109	TCTTCCCTACTTTGC[A/G]CTTAGTTATGCCTTT	88455
rs370762307	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110018231	GAAGTCCGTTGTTTG[A/T]TGGTCACCATCTTGC	88455
rs370789667	snp	C/T	0.000153988	0.00877328	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012036	ACCCACGAGGTCGAA[C/T]ATTATTGCATCTTGC	88455
rs370824142	in-del	-/CTG			intron-variant	ANKRD13A	GRCh38.p7	12:110020667	CTTCCGCATACCCTT[-/CTG]CAGACAGGGAGGCCC	88455
rs370853910	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029081	TAAAATTACTTTGCC[A/G]TGAAAGCTAACAGTA	88455
rs370866127	snp	A/G	0.000198567	0.00996213	intron-variant	ANKRD13A	GRCh38.p7	12:110027796	TGAGCTTTCATTGCA[A/G]TTAGATGAAAGGAAA	88455
rs370992212	snp	A/G	1.65427e-05	0.00287595	intron-variant	ANKRD13A	GRCh38.p7	12:110018510	GACTTCTCTTGTAGT[A/G]ATCACTGCTCAAGCA	88455
rs370997872	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110019546	TTAGAAGACTTAACC[A/G]ACATGAAGAGTATGA	88455
rs371023894	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001578	CTCAGTAGCTGGGAT[C/T]ACAGGCTAATTTTTG	88455
rs371029171	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110030318	ATTATAGGCATGCAT[A/C]ACCACGCCCAGCTAA	88455
rs371109780	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110034432	GGACAGACCTGTGTA[A/C]GCAGTAGGCTTTGTG	88455
rs371304138	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110035325	TAGAAGAATTACTGG[A/C]TGGGTGCAGTGGCTC	88455
rs371318947	snp	C/T	9.89169e-05	0.00703197	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019191	CAAAGTGGTCACCAC[C/T]GAACGCTTCGACCTT	88455
rs371437158	snp	C/T	0.00676609	0.0577691	intron-variant	ANKRD13A	GRCh38.p7	12:110021613	GTATTTTTGTAGAGG[C/T]GGGGTTTCACCACGT	88455
rs371533372	snp	A/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038821	CATACAGAACCCTGG[A/G]GAATACAGCCAAGGG	88455
rs371655787	snp	A/C/G	0.000654585	0.0180794	intron-variant	ANKRD13A	GRCh38.p7	12:110023965	CTTAAGCTGGGGGGG[A/C/G]AAAAAACTATAAAGG	88455
rs371671006	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110037211	GTATACAACACCTAC[A/G]CCGCCAGTTATGTGG	88455
rs371714036	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110014513	TTGTATTCTTTGCTT[C/T]AAGTTATAGAGAGCC	88455
rs371822982	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002890	CCAGCCCCAATCCCA[C/G]TGTCTCACTAATAGC	88455
rs371856022	snp	C/T	0.000207139	0.0101748	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030712	TGGCTGTAGCACTGC[C/T]GAAGAATCTGTATCT	88455
rs371930370	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002667	AGCAATAAAGTGGCT[-/G]GTTTCCCTTAATGTT	88455
rs372014336	snp	A/G	0.000153988	0.00877328	intron-variant	ANKRD13A	GRCh38.p7	12:110012154	TAAGTATACTTTTAC[A/G]ATAATTTAAAGTCCG	88455
rs372082454	snp	A/G	0.000220356	0.0104943	intron-variant	ANKRD13A	GRCh38.p7	12:110033779	ACTCAGACACTGGAC[A/G]GTTGCCTTTTGTTTC	88455
rs372209477	snp	A/G	6.59304e-05	0.00574116	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019252	TTGATGAAGCCAAAA[A/G]GCAGGGAAGTTGAGC	88455
rs372229545	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110024980	GTTTTCTCTACAGCT[C/T]ATAAGTCTATAGAGA	88455
rs372283583	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110023834	CTTTCTATGCCTGGG[A/G]TGAGGCAAATTGATT	88455
rs372319311	snp	C/T	0.000181197	0.00951659	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029568	AATGGCTCGAACGAG[C/T]GCTCATTTTGCAAGA	88455
rs372382362	snp	C/T	0.000910332	0.0213152	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999712	GGCCTGCGACGCGGG[C/T]GACCACTACCCCCTG	88455
rs372436292	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110008569	GAAACATTGGTATTA[A/G]TTCTTTAAATGTTTA	88455
rs372521637	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	ANKRD13A	GRCh38.p7	12:109999291	CTCTGTTCTGTGGGC[G/T]GCACTGAGTTTCTCG	88455
rs372570020	in-del	-/TGTT	0.0333695	0.124785	intron-variant	ANKRD13A	GRCh38.p7	12:110019769	TACTATATAGTTAAA[-/TGTT]TGTTTGTTTGTTTGT	88455
rs372758335	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110006916	TTTGTTCTTTTGCAT[A/G]TAGATATGCAGTTGT	88455
rs372805141	snp	G/T			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039077	TGTTTTGTTTTTTTT[G/T]TTTGTCATTGTCTGA	88455
rs372834055	snp	C/T	3.30721e-05	0.00406632	intron-variant	ANKRD13A	GRCh38.p7	12:110018296	TTCCTGGCCTAGGTA[C/T]TCTTCTTGGCCCTTG	88455
rs372889145	snp	A/G	0.000181262	0.00951832	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013247	CTCCAAAAAATTCTC[A/G]AGGTATCCATGAAAA	88455
rs372999344	snp	C/T	0.000346086	0.01315	intron-variant	ANKRD13A	GRCh38.p7	12:110016382	AAACCTTTGTCTGCC[C/T]TTCAGGCTCCGGATT	88455
rs373032253	snp	A/G	0.000197664	0.00993947	intron-variant	ANKRD13A	GRCh38.p7	12:110036229	AATTTCTCCTAAGAC[A/G]TATTCATGTCTATCA	88455
rs373100925	in-del	-/TGTT			intron-variant	ANKRD13A	GRCh38.p7	12:110019770	TACTATATAGTTAAA[-/TGTT]TGTTTGTTTGTTTGT	88455
rs373279344	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110010156	ACAGGCATGAGCCAC[C/T]GCGCCTGGCTGAGTT	88455
rs373401110	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110017593	TTTGAGAAATGAAAT[A/T]TTTTTCTAATGCACA	88455
rs373452274	snp	A/G	1.8243e-05	0.00302013	intron-variant	ANKRD13A	GRCh38.p7	12:110019356	ACTCTAAATTTTAAT[A/G]TCTAATCCCCATGCT	88455
rs373472910	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001230	TACAGACCTGGTTTT[G/T]GAATGGCTCAAAATT	88455
rs373696454	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110000214	TGTTGTAAGGAAGGG[C/T]TTGGTTGGTTTTGGA	88455
rs373743608	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110027912	TTGAGATACTCTTTT[A/G]GAAGAGAATTAGATG	88455
rs373804069	snp	C/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110029560	ATTGACCTAATGGCT[C/G]GAACGAGTGCTCATT	88455
rs373808938	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001715	ATGAGCCACTGTTGC[C/T]GGCCTTTTTTCATTT	88455
rs373879958	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110002314	GTATTGATTGCATAA[C/T]TAAAAACAAAAAATT	88455
rs373907592	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110005834	TGTGGGTTTCCTTTT[C/T]TTTGAGACAGCTTGC	88455
rs373926911	snp	A/G/T	3.33524e-05	0.00408354	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019151	TAGACAACTGGGCGG[A/G/T]GTTAATGGAAGTCAA	88455
rs373982722	snp	C/T	3.29478e-05	0.00405867	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018412	TGGTGCCAAACTGCG[C/T]GTCGATATCACATTG	88455
rs374043528	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110022475	AAAAAAGAGTGCAAA[C/T]GCTTAGGGCAGTAGA	88455
rs374221837	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110034465	TGTGTGTGTGACTCT[A/G]TGTTGCCCAAGTCGG	88455
rs374364752	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110008225	AGGGATGTTGGAGTT[C/T]TGTCAGATGTTTTTG	88455
rs374383170	snp	A/C	1.65023e-05	0.00287244	intron-variant	ANKRD13A	GRCh38.p7	12:110027697	TTAAACTCCCTACCC[A/C]TCTGTAGCAGACAGG	88455
rs374404529	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026756	GCGTGGTGGCGCACT[C/T]CTGTAGTCTCAGCTA	88455
rs374461686	snp	A/T			missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110030714	GCTGTAGCACTGCCG[A/T]AGAATCTGTATCTCA	88455
rs374520150	snp	A/G	1.65263e-05	0.00287452	intron-variant	ANKRD13A	GRCh38.p7	12:110011986	TCCAATTATGTAAAT[A/G]CCAGTGTTTCCTTCA	88455
rs374523074	snp	C/T	1.66117e-05	0.00288194	synonymous-codon, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033937	ATCCAGCAAAGTCTG[C/T]TGGAGTCCAGCAGGA	88455
rs374538336	snp	C/T	6.58946e-05	0.0057396	intron-variant	ANKRD13A	GRCh38.p7	12:110036370	AAACCAGGGTGAACA[C/T]AGGCCTGGACACAGG	88455
rs374674712	snp	A/G	6.59044e-05	0.00574002	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013180	GTACACAGTTCTCCA[A/G]CATCGAGACTACCAC	88455
rs374857027	snp	C/T	1.65809e-05	0.00287926	intron-variant	ANKRD13A	GRCh38.p7	12:110027816	ATGAAAGGAAACAAC[C/T]TGTCTGTGTCTGGGA	88455
rs374873465	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110023394	GGCTACTTTAAAAGG[A/G]GTTCCACAGAGATGG	88455
rs374895636	snp	A/G	0.00597247	0.0543191	intron-variant	ANKRD13A	GRCh38.p7	12:110026776	AGTCTCAGCTACTGG[A/G]GAGGCTGAGGCAGGA	88455
rs374975049	snp	A/G	8.23961e-05	0.00641804	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110016393	TGCCCTTCAGGCTCC[A/G]GATTTCTATGTGCAG	88455
rs375180009	snp	C/T	0.000153988	0.00877328	intron-variant	ANKRD13A	GRCh38.p7	12:110024127	GGTAAAAGGAAACTC[C/T]TAAAATAAGATTTAA	88455
rs375186462	snp	G/T	0.000875616	0.0209055	intron-variant	ANKRD13A	GRCh38.p7	12:110036207	GTTTCCTTACCAGAA[G/T]GGCACCAATTTCTCC	88455
rs375222313	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110014939	CAGGCGCCCACCACC[A/G]CGCCCGGCTAATTTT	88455
rs375280495	snp	A/G	0.000131843	0.00811815	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110012027	AGGCTGTGGACCCAC[A/G]AGGTCGAACATTATT	88455
rs375741955	snp	A/C	0.000129425	0.00804336	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999716	TGCGACGCGGGCGAC[A/C]ACTACCCCCTGCACC	88455
rs375764788	snp	A/G	0.000153988	0.00877328	intron-variant	ANKRD13A	GRCh38.p7	12:110013256	ATTCTCGAGGTATCC[A/G]TGAAAATGTGGCCAG	88455
rs375783870	snp	C/G			utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999457	GCGAGCTGTCAGCGC[C/G]GGCGGGAACGCCGCG	88455
rs375802634	snp	C/T	0.000182075	0.00953963	intron-variant	ANKRD13A	GRCh38.p7	12:110016485	TAAATTTACTTAGCC[C/T]GCATGTAGGTTTATT	88455
rs375815018	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110020753	CTGCCACTGTTCATC[C/T]GTAGGGATGAGATGG	88455
rs375842463	snp	A/C			upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998655	AACCTCAAATCCAAA[A/C]AGCTAGCTTAAAAAT	88455
rs376124784	in-del	-/GTT			intron-variant	ANKRD13A	GRCh38.p7	12:110036099	TCCCACTTAGGTGTT[-/GTT]TTTGAGGTAACCCAA	88455
rs376341927	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001542	CCTCCCGGGTTCCAG[C/T]GATTCTCCTGCCTCA	88455
rs376596948	snp	C/G	0.00636936	0.0560724	downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039630	AATGGCAACTAAAAG[C/G]AAGCCAGTGTTGGGC	88455
rs376638028	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110027512	ACAACTGTTTATCTA[A/G]TTTAGAGATCCTCAT	88455
rs376652102	snp	A/G	0.000153988	0.00877328	missense, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033859	CCCGAATCTTACTAT[A/G]TTCAAGACAATGGCA	88455
rs376709849	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110034517	CATGATCATATTGCA[C/G]CCTCAAACTCCTGGG	88455
rs376736792	snp	A/G	1.64795e-05	0.00287045	missense, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110019216	GACCTTTCCCAAGAA[A/G]TGGAGCGCCTCACTC	88455
rs376754743	snp	A/G			intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033987	ATACTCTAATGGCAG[A/G]GCGTGGGAGGTCTTA	88455
rs376781751	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110003480	TCAAGATTCCTGTTT[C/G]CACTGACTCAGCGTG	88455
rs376789342	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110000686	GACAGCCCCCCGCAA[C/G]TAAGACTTCTCCGGC	88455
rs376855837	snp	C/T	1.64923e-05	0.00287156	missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018476	AGGCGTAGTTTTATA[C/T]TTAAGGGAGAAGGTG	88455
rs376899067	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110000670	ATCCTACAATGGCCA[A/G]GACAGCCCCCCGCAA	88455
rs376983917	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110035298	ATTGAATTGTGTCTT[C/T]TAATCTTGCCCTAGA	88455
rs377184513	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997175	ACGCCATTGCACTCC[A/T]GCATGGGCGACAGAG	88455
rs377313036	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110005635	TGGAGGTTCATCTAC[A/G]TTGTGGCATGTTTCA	88455
rs377322373	snp	A/G	9.88354e-05	0.00702908	synonymous-codon, missense	ANKRD13A	GRCh38.p7	12:110036281	TTCAGGACCAGCTTC[A/G]AATGGAGGGATCAGC	88455
rs377378520	snp	C/T	3.31181e-05	0.00406914	intron-variant	ANKRD13A	GRCh38.p7	12:110025726	GTCACTGTTTTCTTT[C/T]GCATACACCTCTCAG	88455
rs377428450	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110016037	GCTCTCTGCAGCCTC[C/T]ACCTCCTGGCCTCAA	88455
rs377451135	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029669	CAGCAACACTTGGAG[A/G]TTCTGCCCATGTTTG	88455
rs377474608	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110001369	GCTGTGTGCTTGCAA[-/C]CCTGCCATATTTAAG	88455
rs377650416	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110028957	TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTTG	88455
rs377673931	snp	A/G	4.95021e-05	0.0049748	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110027718	AGCAGACAGGAACCC[A/G]CTGGAATCTTTGCTG	88455
rs377683122	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110000347	CCAACACTTGACTCT[A/G]TTGATAGGTCTGGGG	88455
rs527268128	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110001404	TTGAGCCCTCACCGA[A/G]GTCCAAAATTACCCT	88455
rs527346694	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110008686	GGTTAGGAGTTCAAG[A/G]CCAGCCTGGCCAACA	88455
rs527434424	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110034745	CTCTACTAGGGTAGG[A/G]TCTGGTCTGCCTCCA	88455
rs527697386	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032913	ACTATTAGGATGATA[C/T]ACATGTGGCAAGCTC	88455
rs527741020	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	ANKRD13A	GRCh38.p7	12:109999241	TAGACGGAACTTTCC[A/G]CGTGGAGATCTTTGG	88455
rs527809999	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110010413	CTAAACTTCAACTGA[A/G]TTTATAGTTCATAAG	88455
rs527882498	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026147	TTTGTATTTTCAGTA[C/G]AGACGGGGTTTCACC	88455
rs527891439	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016549	AGTCAAGGAAATACA[G/T]AGTGAAGAATAAGGA	88455
rs527936331	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110011207	AGGCAGTGCCCAGGC[A/G]TTGAGACTTAGCTCA	88455
rs528077157	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110013640	GCAGGGCATGGTAGT[A/G]CATACCTGTAGTCTG	88455
rs528092603	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110023061	AACCGCATATGTTCT[C/T]TGTAACGTGGCTAAC	88455
rs528149483	in-del	-/T	0.398174	0.201356	intron-variant	ANKRD13A	GRCh38.p7	12:110021426	TTTCTTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT	88455
rs528151489	in-del	-/TGCT			intron-variant	ANKRD13A	GRCh38.p7	12:110017037	CCTAGCCCCCCAAAG[-/TGCT]TGCTGGGATTACAGG	88455
rs528172844	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030820	AAATTTATGGCCGGA[C/T]GTGGTGGCTTATGCC	88455
rs528214710	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022365	GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGGC	88455
rs528236043	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110032854	TTGAAGAATAAATTC[C/T]GCATGATTCCATTTA	88455
rs528272303	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110008338	ATTCTTATATTTGTA[C/G]GATAAGTCTCAGTTG	88455
rs528353518	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110014320	AGGAGGCTGAGGCAG[A/G]AGAATGCTGTGAACC	88455
rs528404352	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110006888	GGGATGAGCCAATGA[A/G]CTCAGCCAAAATTTT	88455
rs528491615	snp	A/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110005003	ATAAACATATACAGA[A/T]TGATTTTTTCAAAAG	88455
rs528557218	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110021376	GATTGAATTTGGAAG[G/T]TGTGGCCTTCTCTCA	88455
rs528631995	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004220	TGAGCTGAAATGAGC[A/G]AATAGGAAGGAAACT	88455
rs528652452	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038520	ACTCCAGAGGAAGGA[C/T]TGATTTGCAACCAGA	88455
rs528886607	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110015292	CTAGCAACCTCTTTC[A/G]GTTTCACAGAGTAGT	88455
rs529021281	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110014516	TATTCTTTGCTTCAA[A/G]TTATAGAGAGCCTGT	88455
rs529154443	snp	A/C	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110007611	TCTCGAACTCCCGAC[A/C]TCAGGTGATCCGCCC	88455
rs529179151	snp	C/T	0.0023933	0.0345097	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999456	CGCGAGCTGTCAGCG[C/T]GGGCGGGAACGCCGC	88455
rs529237445	in-del	-/T	0.131723	0.220251	intron-variant	ANKRD13A	GRCh38.p7	12:110001437	TTTCTTTTCTGTTTC[-/T]TTTTTTTTTTTTTTC	88455
rs529246126	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110022504	GAGGCAGGATTGCCG[A/G]AGGAGCAGAGGTAGC	88455
rs529336685	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005327	TTAAAGATTTTTTTG[C/T]AGAGAAAATGTGTCC	88455
rs529415741	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005935	GATTCTCCTGTCTCA[C/G]CCTCCCTAGTAGCTG	88455
rs529438960	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039822	TATATCTAAATAAGC[A/G]GGTATTAAAAACAAC	88455
rs529527126	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032033	CTTTTTCCTTTCTAA[A/T]CTTTAAGCTTTTCAT	88455
rs529550077	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039043	CAAAGAATTGTGCTT[C/T]TAATTCCATTTCACA	88455
rs529564662	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998091	CAATAAACACGGCAT[A/G]ATGAAGAAGAAGGAG	88455
rs529636396	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110008834	AGGTTGCAGTGAGCT[A/G]AGATTGTGCCACTAT	88455
rs529653196	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028911	CCCAGCTAATTTTTG[C/T]ATTTTTAGTAGAGAT	88455
rs529680432	snp	C/T	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110023751	ACTTCTTTGGGACTG[C/T]TGTCCAATAAATGTC	88455
rs529854371	snp	A/C	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110012765	AGTAATTTTGTGTTG[A/C]CTGAGCAGGGATACT	88455
rs529913834	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110029734	GGAATTGGAGTGCTT[C/T]AGGTCAAAGTAGCTT	88455
rs529975180	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110021511	GCTCACTGCAACCTC[C/T]GCCTACCGGGTTCAA	88455
rs530176735	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001888	ATTTAATTCCTTTTC[C/T]ATTACTAGACATGGT	88455
rs530219320	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004051	TAATCCCAGCTACTT[A/G]GGAGGCTGAGGTGGG	88455
rs530238925	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110004438	CTGACCAACACAGAG[A/G]AACCCCGTCTCTACT	88455
rs530351252	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110003100	GAAGTCTGTTAAACT[C/T]CTTTGGCCTTCTTAC	88455
rs530450094	snp	A/C	5.07061e-05	0.00503492	intron-variant	ANKRD13A	GRCh38.p7	12:110030767	GATTCAGGTAAAAAA[A/C]TAAATAAATACAAAG	88455
rs530569576	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030015	TGTAAATATGATCTA[C/T]GTCCCAAGCTAGTAT	88455
rs530613454	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110006041	AGGCTGGTCTTGAAC[C/T]CCTGACCTCAAGTGA	88455
rs530614744	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110014262	CTAAAAATACAAAAA[A/G]TTAGCCGGGTGTGGT	88455
rs530677923	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038842	CAGCCAAGGGCACTG[C/T]TCACTGTGGCCCGTG	88455
rs530800600	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110001657	ACCCCTGGCCTCAAG[C/G]AATCCGCCCACCTCT	88455
rs530987936	snp	A/C/G	0.000378921	0.0137596	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110013171	TGAGATGGTGTACAC[A/C/G]GTTCTCCAACATCGA	88455
rs530999425	snp	G/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110019861	TTCAGTTCTGTTCCA[G/T]ACTCATAAAGAATTC	88455
rs531062611	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020389	AATGTGTTTAGTCAA[C/G]CATAAAACTTGTTAA	88455
rs531069523	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004119	GCCAAAATCGCACCA[C/T]TGCACTCTAGGCCCG	88455
rs531264778	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004861	CTAAGTTAAGGACTT[A/T]CCCCTTGTAAGAACT	88455
rs531400644	snp	A/G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015971	TTTTTTTTTTTTTCC[A/G/T]TACAGTATCTCGCTC	88455
rs531403105	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001448	TTTCTTTTTTTTTTT[C/T]TTTCTTTTTGAGATG	88455
rs531416006	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110027994	GAAATCAGGTGCTTT[C/T]CCTCTTATCCATTAT	88455
rs531617488	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035725	AAAGTGCTGGGATTA[C/G]AGGTGTGAGCCACCA	88455
rs531621976	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034343	GAAGTGGATTTGAAT[C/T]CCACTTCCTCCACAA	88455
rs531747282	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110015027	GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC	88455
rs531963134	in-del	-/TTTG	0.00119737	0.0244387	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039137	ATAGGCAACGTCACA[-/TTTG]TTTGTTTCAAATATG	88455
rs532040638	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002831	AAGAAAGAATCAAGT[C/T]TATCCAGATGAAGAG	88455
rs532124021	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110015331	TAGGAAGCACTTGCC[A/C]GCACACAAACCTTTT	88455
rs532257405	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110037280	TGTGCCCTTGGTAAG[C/T]GGTTAAGAAATGTAG	88455
rs532378671	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110017662	ACTTAGGCCGGATGC[A/G]GTGGCTCATGCCTGT	88455
rs532419201	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028072	CTTTATATTGCAACA[A/G]AGCACCTTAACAAAT	88455
rs532598468	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110007748	TTTTATATTTATTGT[A/G]TCATATTTATTCCTA	88455
rs532619025	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110034595	TCATGCACCACTGTG[C/T]CCAGTAGAACAGTTG	88455
rs532728286	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110037033	CCAGAGATTACGGGA[A/G]AAACCGCGAGGATTC	88455
rs532740231	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002120	TATACTTCTTTCAGT[A/G]AAAATGACTTCATTT	88455
rs532805365	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110035187	TTTCCCTATGTAAGT[A/G]AGCTTAGCTCCCCCC	88455
rs532862340	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110025264	TGGAGGCTGAGGCAC[C/G]AGAATCGCTTGAACC	88455
rs533033902	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015461	TTCCCAGGTTCATCT[G/T]TCTCTTACTGTTAGG	88455
rs533040595	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019642	ATTTTTGTCTTAGTG[A/T]TTATGGATCCACAAT	88455
rs533096315	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007714	TTAAACAATGTTTTA[A/T]GGTTTAAGAGTATGT	88455
rs533212176	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110000135	CCGGCTGGCTCCGGA[A/G]TGCACCGTCTTAACC	88455
rs533423351	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110006826	ATCTCGAACTCCCTA[C/T]CTCAGGTGATCCTCC	88455
rs533486532	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998233	ATCACAGAATTCCCA[C/T]GCATTCCATGGTTAG	88455
rs533727010	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032796	TATGTGCGTCAAAAC[A/T]GTTGAATTTCAAAAG	88455
rs533794813	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033358	TGAGCCACCGCGCCC[A/G]GCAGTTATTGATAGT	88455
rs533837579	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:109999623	GGCAGGCAGGCGGGC[A/G]CGGGAGACCCCGCCG	88455
rs533924587	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026027	AGTGCAGTGGCACGA[C/T]CTTGGCTCACTGCAA	88455
rs534389617	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012290	GGATCACCTGAGCCC[C/G]GGGAGGTTGACACTG	88455
rs534394593	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998747	AGTTCAAATAGAAGC[A/G]GTTCTCAACTGAGGA	88455
rs534536009	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039136	TATAGGCAACGTCAC[A/G]TTTGTTTGTTTCAAA	88455
rs534536430	snp	C/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110007132	TTTAAAATTGGCAAG[C/T]GTGAAATGTGAGTCC	88455
rs534755664	snp	C/T	1.6477e-05	0.00287024	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110028535	CACGGAATGTGCTAC[C/T]GCAAACAACCCCACA	88455
rs534766749	in-del	-/A	0.000209047	0.0102215	splice-donor-variant, intron-variant	ANKRD13A	GRCh38.p7	12:110030760	CAGGCTGATTCAGGT[-/A]AAAAAAATAAATAAA	88455
rs534781921	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110023372	TGCATCTGCCACTGG[A/C]ATGCTGGGCTACTTT	88455
rs534822342	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110025288	TTGAACCCAGGAGGC[A/G]GAGGCTGCAGTGAGC	88455
rs534861177	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110029085	ATTACTTTGCCATGA[A/G]AGCTAACAGTAGATT	88455
rs534924801	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020941	AGAGACATTGTTCCC[C/T]ATATTGTTCAACAGT	88455
rs535047176	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036894	TGCCATTGGGGGAAA[C/T]GTACTGAGTCAGTTT	88455
rs535086973	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997613	AGGAAGAAGAATATG[C/T]GACAAAACTTGTATG	88455
rs535247104	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030177	CTCATTTTCTCTTTT[A/T]TTTTTTTGAGATGGA	88455
rs535334553	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998314	CTCACAAATCTTCTG[G/T]GCTCCACATCTGTGG	88455
rs535444982	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037985	TGTGATCTATGAGAA[C/T]TGGAGACACTTCTTT	88455
rs535454469	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110024936	ATTTTTGTCAGTGCA[C/T]AGAATGCCTTTTAAA	88455
rs535513547	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110013741	GAGTGAGGGTGCAGT[A/G]ATCGCACCCCTGCAC	88455
rs535587756	snp	G/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110020204	TGGACGCTATTATCC[G/T]TATAGTATTTGTCTA	88455
rs535664791	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110032550	CCTTGAATAAAACAT[A/T]CGGCATTACTGTATA	88455
rs535681084	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110013026	TGCAGCCCTTTTCTT[C/T]TGAAGAAAATACTGG	88455
rs535883629	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110020084	CCAGCTTTCTGCAAG[C/T]CAAAGTAGCTTAGCC	88455
rs535916976	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110003909	CACGCCTGTACTCCC[-/A]GCTCTTTGGGAGGCC	88455
rs535930703	snp	C/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110036698	GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG	88455
rs535932521	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110027465	GCTCACTCCAAAATC[C/T]AGACTCTTCCCATTA	88455
rs536071996	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022391	GAGGCGGAGCTTTCG[A/G]TGAGCTGAGATTGCA	88455
rs536117703	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020697	CCCCTTCAGCTTAGG[G/T]CTCTGTTCATAACCC	88455
rs536141625	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110030386	TGGTTAGGCTGGTCT[C/T]GAACTCCTGACCTCA	88455
rs536252396	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110001604	TTTTGTATTTTTAGT[A/G]GAGGTGGTATTTTGT	88455
rs536324911	snp	C/T	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110017788	AATACAAAAATTAGC[C/T]GGGCATGATGGTGGG	88455
rs536386751	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110011621	TATTCTAGACTTGAA[C/T]GCTGATATGTGCTTG	88455
rs536456011	snp	A/C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004314	GAAAACCTAAATGAT[A/C/G]AGTTTCGAAAGTGAA	88455
rs536592866	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110020357	TTCTTTTCTTTCTAG[C/T]ATAAAATTGGTTAAT	88455
rs536646912	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110003468	AGGAAACTGGCCTCA[A/G]GATTCCTGTTTCCAC	88455
rs536729512	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110008923	CATTTTTTTTGGTGG[A/G]CAGTTTTAAAATTAC	88455
rs536792580	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110035685	AAACTCCAGACCTCA[A/G]GTGATCCACCAGCCT	88455
rs536794634	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110020728	CAGAAGGCAGAGGAA[A/G]CTGCCTTTTCTGCCA	88455
rs536833684	snp	G/T			splice-donor-variant, intron-variant	ANKRD13A	GRCh38.p7	12:109999786	AGCTGCAGGGCCAGG[G/T]GAGGGGCGGGGCGGG	88455
rs536916136	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110027918	TACTCTTTTGGAAGA[G/T]AATTAGATGAGTGAC	88455
rs536917472	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110004414	TGAGGTCGGGAGTTC[A/G]AGACCAACCTGACCA	88455
rs536918161	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110012818	GGTCTACATATAACC[A/G]CAGTTACATGTTGTG	88455
rs537119788	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010480	CAAGTTAGAGACTAA[A/G]GTAAGAGAATCTAGA	88455
rs537132096	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028973	GAACTCCTGACCTTG[A/T]GATCCGCCCGCCTGG	88455
rs537182726	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002446	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	88455
rs537191353	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001043	ATTACAGGTGTGAGC[C/T]ACCACGCCTGGCTGA	88455
rs537207045	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036716	GATCGCGCCACTGCA[C/T]TCCAGCCTGGGCGAT	88455
rs537267779	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110028426	TTTAGCTGGTTAACA[C/T]GTCCACCTCAGACAC	88455
rs537449435	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110003321	GGTTCTCACTCCAGC[C/T]TGGGGCAGGCCAGGT	88455
rs537647716	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110027199	TTGTGAAATTACTTC[A/T]GCTCTGTGCCTTAGT	88455
rs537671840	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037783	ATCTCCAGGCTAAGG[A/G]GAGGAGAGCATCATC	88455
rs537784960	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110023804	GCAGTTTTGTAAAGA[A/C]GCCAAGATTGGAGGC	88455
rs537809163	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034044	CTAATCTGAAAGATT[C/T]ATTCTAAATATCAAG	88455
rs537938710	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033178	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	88455
rs537998464	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110024921	CTGGCAGTTACAATA[A/G]TTTTTGTCAGTGCAC	88455
rs538049343	snp	C/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110018678	GCTAGCTCTCCTTCA[C/T]GTGTCCTTTACCACC	88455
rs538052792	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110009769	CCTCTGTGGTCCGAA[C/G]TAGAAAAAAAGTTAA	88455
rs538174612	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110009639	CACTGTCATCATAAT[A/G]CAATTACAGCATTTT	88455
rs538183639	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110008296	TGATATGGTGTAATA[C/T]GTTAATTGACTATCT	88455
rs538190629	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110008792	CAGGAGGCTGAGGCA[C/T]AAGAATCACTTGAAC	88455
rs538191411	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110017842	GAAGCTAAGGCAGGA[A/G]AATCGCTTGAACCTG	88455
rs538191445	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026986	ATTCGTGAGGGCTTG[C/T]TTATGTGTTATCAAG	88455
rs538340833	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035155	TGCACATCACCATCA[A/G]CCTGGTATGCTTTTC	88455
rs538502588	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007984	TTCTGGATGCTTTTT[A/G]TTTATTTTTCTTGCC	88455
rs538582239	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110026532	TGGTGAGCTGAGATC[A/G]TGCCATTGCACTCCA	88455
rs538692179	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110008899	GGAAAAAAAACCCAT[C/T]TGGGCCTGCATTTTT	88455
rs538742035	snp	C/T	1.64852e-05	0.00287094	synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110025759	TTACACAGTAAACAA[C/T]GTGAATGTGATCACC	88455
rs538793328	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016645	TTCCCCGCCATGCAT[A/G]GGACTTTTCCTCCCA	88455
rs538864379	snp	A/C	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110026371	CTGAGGTCGGGAATT[A/C]AAGACCAGCCTGACC	88455
rs538920862	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110009502	TCTAACTAAATGTTC[A/G]TCAATGTTGTTGACA	88455
rs538928619	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110000537	TGCTCTCAGTTGGAG[A/G]TGATTTTGCACCCAC	88455
rs538970873	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020042	GAGTCCTAAGAGCAC[G/T]GATAGTATTTGCCTA	88455
rs539291933	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110000673	CTACAATGGCCAAGA[C/T]AGCCCCCCGCAACTA	88455
rs539345277	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002412	GCCTGAGGTCAGGAG[C/T]TGGAGACCAGCCTGA	88455
rs539405828	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039073	AATCTGTTTTGTTTT[G/T]TTTTTTTGTCATTGT	88455
rs539514611	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110007048	TCTAAATTGTATTCC[A/C]TTGACCTGTATGTCT	88455
rs539545010	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038678	TATTTGTAAAAGATA[C/T]AAAAACAACTCCCAT	88455
rs539578011	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110033320	GCCTGCCTCAGCCTC[A/C]CAAAGTGCTGGGACT	88455
rs539590840	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110013733	CCACCCCTGAGTGAG[C/G]GTGCAGTGATCGCAC	88455
rs539657334	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110006354	GTACGCATCCTAGTG[A/G]GTGTGAAGTGGCATC	88455
rs539790123	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110023517	CCTAATGGCATCTCC[A/G]AGCAGCTCACCACAG	88455
rs539821467	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110017256	ATAAGTAGATTTACC[A/G]TAATTTACTAATTTC	88455
rs539839432	snp	C/G	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110031022	ATCGCTTGAACTGGG[C/G]GAGAGGCGGGGGGAT	88455
rs540050706	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110014806	TTTTTTTTTTTGAGA[C/T]GGAATCTCGCTCTGT	88455
rs540055588	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110008410	GTTTGCCAGTATATC[A/G]TGGAGGATTTTTGCA	88455
rs540200431	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110032733	GCGCTATTGTGCTCT[A/C]TTAATACAACAGAAT	88455
rs540332030	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110031837	AATTGAGTTTTGTAT[G/T]TTGACCTTGAATCGT	88455
rs540485977	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110036645	TAGTCTCAGCTACTC[A/G]GGAGGCTGAGGCAGG	88455
rs540512335	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110015170	CTAAACAGGGCTGCT[A/G]TGGTAGTTTAAAACT	88455
rs540649051	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110005904	TCTCTGCAACCTCTG[C/T]CTCCTGGGTTTAAGC	88455
rs540707378	in-del	-/CCT	0.00199481	0.0315187	cds-indel	ANKRD13A	GRCh38.p7	12:110038903	CCTGGTAAACAACAC[-/CCT]CCTCCATTTTGCGTC	88455
rs540708280	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110004604	CCATTGCACTCCAGC[C/G]TGGGCAACAAGAGGG	88455
rs540711396	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022216	GCACTTTGGGAGGCT[A/G]AGGCGGGTGGATCAC	88455
rs540779271	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13A	GRCh38.p7	12:110007541	ATGTGCCACCACGCC[C/T]GGCTAATTTTGTATT	88455
rs540852591	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110030459	GGTGTAAGCCACCGC[A/G]CCTGACCGAAAATAC	88455
rs540908378	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110006633	TGGAGTTTCGCTCTT[A/G]TTGCCTAGGCTGGAG	88455
rs540927990	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038228	GCCTTAGCCTTAAAC[A/G]TTACTAATAGTTTCA	88455
rs541093161	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110027827	CAACTTGTCTGTGTC[G/T]GGGATGGCATTTACT	88455
rs541234882	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022117	AAAATTTAAAACAGG[G/T]TATGAACATTGGGTT	88455
rs541239681	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011512	ATACACAATAATGAG[A/G]GTGGTGTTTTGGTGG	88455
rs541432116	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038395	TTCTTGAAGTGGGCA[A/G]GCTGGCCAAAATATT	88455
rs541535199	in-del	-/T	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110014013	TTCTCCTTGCCAGGC[-/T]TTGTCACTTCAGCTA	88455
rs541540194	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005787	TTGGCTATTATGAGT[A/G]ACGCTGCTGTGTGTA	88455
rs541540641	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035568	GATTCTCATGCCTCA[A/C]CCTCCCGAGTAGCTG	88455
rs541645872	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110022979	AACTCATTATACCAT[A/C]TGGACTAATTTCATT	88455
rs541660762	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110031477	TTGCCTAGTCTCCCA[A/G]GTAGCTGGGAATACA	88455
rs541689921	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110014739	TCATGGCAAAGCCTT[A/G]CAAGTGTGTAGGAAT	88455
rs541754706	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110039332	GAATTCACTTAAAAA[C/G]GGACTGAGCATTGTG	88455
rs541845312	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038778	AACTCTCTTTTGTCA[A/G]ACCCTCTTGTATATA	88455
rs542212838	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010136	CCTCCCGAAGTGCTG[A/G]GATTACAGGCATGAG	88455
rs542266440	snp	A/C	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110029225	CACCCGCTATCATTT[A/C]TTCATGCTTGCTGTC	88455
rs542416919	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110004774	GTGACAGCTATATGA[A/T]ACTACATAGTGTGGG	88455
rs542426373	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001298	GGATTGTTTGTCTTA[C/T]GGTTGACAAAAATTG	88455
rs542492677	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110036432	CTCAGGCAGATGTAC[A/G]GTGCCACAAACTGGC	88455
rs542632816	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110010866	TCTTCAGAGACTGCA[-/G]GGGTAGTTAGTACCT	88455
rs542756006	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110000826	GCAATGGTGCGATCT[A/C]GGCTCACTGCAACCT	88455
rs542774228	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026151	TATTTTCAGTAGAGA[C/T]GGGGTTTCACCATGT	88455
rs542774345	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035216	CCGCCAGCTCCCAAG[G/T]AGCTTCATAAACCTT	88455
rs542839923	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026634	CACCTGTAATCCCAA[C/T]ACTTTGGGAGGCCAA	88455
rs542897586	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110002045	TCAGCCTCCCAAAGT[C/G]CTGGGATTACAGGCA	88455
rs542913365	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034247	TTTTTGAGATGTGCT[C/T]CATCATTTTCTAGCA	88455
rs542921359	snp	A/T	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110002702	TTGCTGGTGAGTTTC[A/T]GCTGTCAGTTTCCTC	88455
rs542956973	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110032442	ACCTTTACATTCCCA[C/T]GTAGCAACAAAGTTG	88455
rs543099571	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010944	TGTATTATGGCATTT[A/T]AAAAGTTTTTACAGG	88455
rs543121520	snp	A/G			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997250	CGGGCGTGGTGGCGC[A/G]TGCCTGTAATCCTAG	88455
rs543202566	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110002751	TTGAGACTTGGAGCA[C/T]GTATACTGATAGCTG	88455
rs543220821	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110037056	GAGGATTCATTTTAC[A/G]AAGACTTATACTTAA	88455
rs543358333	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110025986	TTTTTTTTTGAGGCA[A/G]AGTCTCGCCCTGTCA	88455
rs543416997	snp	A/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110003868	TCTCCTTAAAAAAAA[A/T]TTTTTTTTGGCTGGG	88455
rs543461767	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110032039	CCTTTCTAATCTTTA[A/C]GCTTTTCATTTCTTT	88455
rs543484064	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110035411	GGAGTCTGAGACCAG[C/T]CTGGGCAACATAGTG	88455
rs543568849	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110018233	AGTCCGTTGTTTGAT[A/G]GTCACCATCTTGCCA	88455
rs543634447	snp	G/T	0.00119737	0.0244387	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038052	TCCTTATTTTTACCT[G/T]TTTACAGGGTTTCTA	88455
rs543736334	in-del	-/TTG			intron-variant	ANKRD13A	GRCh38.p7	12:110020977	TGCCAGAGTCATTGT[-/TTG]TTGAAGTGCGATTTG	88455
rs544184543	snp	C/T	0.00318978	0.0398085	intron-variant	ANKRD13A	GRCh38.p7	12:110025256	AGCTACTCTGGAGGC[C/T]GAGGCACGAGAATCG	88455
rs544250148	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026053	TGCAACCTCTGCCTC[C/G]TGGGTTCAAGTGATT	88455
rs544250267	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110016181	CTCAAACTCCTGAGC[A/G]CAAGTGATCACCCGC	88455
rs544489506	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110007483	TCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA	88455
rs544633493	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016966	TTAGTAGAGAGTGGG[G/T]TTTCACCATGTTAGC	88455
rs544675044	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110014228	CCATCCTGACTAACA[C/T]GGTGAAACCCCATCT	88455
rs544700124	snp	A/G			missense, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110033823	ACAAACTTTGAGGTT[A/G]ATCAATCTGTGTTTG	88455
rs544770093	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026122	ACCCACCACCACGCC[C/T]GGCTAATTTTTTGTA	88455
rs544954430	snp	A/G	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110001479	GAGTCTCGCTCTGTC[A/G]TTCAGACTTGAGTGC	88455
rs545005967	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110017927	ACAGGGTGAGACTCC[A/G]TCTCAAAAAAAAAAA	88455
rs545085009	snp	C/T	0.000715435	0.0188999	intron-variant	ANKRD13A	GRCh38.p7	12:109999806	GGCGGGGCGGGGGTC[C/T]GTCTCCCGGTGGGGA	88455
rs545277955	in-del	-/T	0.471757	0.115429	intron-variant	ANKRD13A	GRCh38.p7	12:110016282	CTTCTTATTTTCTCT[-/T]TTTTTTTTTTTTAAC	88455
rs545300393	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110009990	CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGACAAT	88455
rs545460104	in-del	-/TTG	0.00398564	0.0444627	intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034121	TCTTCTTACAAAAGC[-/TTG]TTGTTATGTAAGAGA	88455
rs545523956	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	ANKRD13A	GRCh38.p7	12:109998999	TCGCCAGGGTTTAGC[G/T]TTCCTCCTTCAAAAA	88455
rs545553075	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997781	ATTACTGTTTTTCTT[C/T]ATATGCGTGGAATTT	88455
rs545608933	snp	G/T	0.00398564	0.0444627	intron-variant	ANKRD13A	GRCh38.p7	12:110015132	TTTAGGAACTTACAG[G/T]AATGGTAGGTAAGAA	88455
rs545633105	snp	A/G	1.71675e-05	0.00292976	intron-variant	ANKRD13A	GRCh38.p7	12:110023968	AAGCTGGGGGGGAAA[A/G]AAACTATAAAGGCTA	88455
rs545771774	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110032694	AAACCTGGAAACGAC[A/C]CAAATGTCCCGAGAT	88455
rs545785036	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039501	CCACACTTCCTGTTA[C/T]GTATGTCAGTAGAAC	88455
rs545917751	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038854	CTGCTCACTGTGGCC[C/T]GTGTATTCATTCCCA	88455
rs546071308	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110023050	AAAATGCTAATAACC[A/G]CATATGTTCTTTGTA	88455
rs546097272	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110007911	TTTAATAGTTCTAAT[A/C]GTTTTTTGGTGGATT	88455
rs546178380	snp	C/T	0.000135658	0.00823471	intron-variant	ANKRD13A	GRCh38.p7	12:110021121	AGGGTTTTCAGAGTT[C/T]TCAAGCTAACTCTTT	88455
rs546209361	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110006185	CTTGGAGAGGAATTG[C/T]TGGGTCATGTAGTTA	88455
rs546241735	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110012555	AGAATGACTCCTCAT[C/T]CAGAAACAGCTCTCA	88455
rs546244098	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110023328	TATGTTGAGTTGAAT[A/G]ACTGAGATTTTGGGC	88455
rs546345140	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998281	CTGGTGCTCCTGCAT[A/C]CTGTTTTGGTTTAAC	88455
rs546408430	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-5-prime	ANKRD13A	GRCh38.p7	12:109999290	GCTCTGTTCTGTGGG[C/G]TGCACTGAGTTTCTC	88455
rs546503646	snp	C/G			utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037868	CAAAACCCCAATCCC[C/G]GCAGGTTTGTAGATA	88455
rs546534946	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110013649	GGTAGTGCATACCTG[C/T]AGTCTGAGCTACTTG	88455
rs546545240	snp	A/G	0.000960328	0.0218916	intron-variant	ANKRD13A	GRCh38.p7	12:110018522	AGTAATCACTGCTCA[A/G]GCAAAATTACAGGGT	88455
rs546672003	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13A	GRCh38.p7	12:110022381	GTGAACCCAGGAGGC[A/G]GAGCTTTCGGTGAGC	88455
rs546692474	in-del	-/A	0.139225	0.224118	intron-variant	ANKRD13A	GRCh38.p7	12:110022449	GTAAGAGTCCATCTC[-/A]AAAAAAAAAAAAAAA	88455
rs546771354	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110012687	AAATTGTGGCTAAAA[A/G]TAGCCTCTTCCTGGG	88455
rs546971033	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110005188	ACAGGGTCTCACTCT[C/G]TTGCCTAGGCTGGCA	88455
rs547116848	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110028101	ATATTTTCTTACTTG[A/T]TGCTCACAGTAACTA	88455
rs547168968	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110000199	ATAGCACACTCTCCT[G/T]GTTGTAAGGAAGGGC	88455
rs547189269	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110030240	GGCATGATCTTGGCT[C/T]ACTGCAACCTCTGCC	88455
rs547230376	snp	C/T	0.0023933	0.0345097	intron-variant	ANKRD13A	GRCh38.p7	12:110002029	AAGTGATCTGCCCGC[C/T]TCAGCCTCCCAAAGT	88455
rs547231660	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110019547	TAGAAGACTTAACCA[A/T]CATGAAGAGTATGAA	88455
rs547250781	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110030821	AATTTATGGCCGGAC[A/G]TGGTGGCTTATGCCT	88455
rs547293118	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110028877	TGAGTAGCTGGGACT[A/G]CAGGCGCGTGCCACC	88455
rs547329568	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038551	AAGGGAGCTGAAAAC[C/T]ACGGAGCTCCATGGC	88455
rs547417794	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110009534	TTTCCAAGAACCAAC[G/T]TTTGGTTTTGTTGAT	88455
rs547437934	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110017721	GGAAGATCACCTAGG[A/T]CAGGAGTTGAAGACC	88455
rs547598419	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110002990	TAAAGTGCCTCTTAA[C/T]CCATCAGCTCATTAA	88455
rs547677215	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010379	GAAGATAATGAGTTT[G/T]CTAATTATTTCTTTC	88455
rs547795643	snp	C/T	6.59435e-05	0.00574172	synonymous-codon, intron-variant, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018469	AAGAGGGAGGCGTAG[C/T]TTTATATTTAAGGGA	88455
rs547814466	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110020711	GGCTCTGTTCATAAC[C/G]CCAGAAGGCAGAGGA	88455
rs547814522	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110029852	AAGAGATCTCCAACC[A/G]TCATTTCTATTTGCA	88455
rs548073637	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13A	GRCh38.p7	12:110021518	GCAACCTCCGCCTAC[C/T]GGGTTCAAGCAATTC	88455
rs548187083	snp	A/G	2.1585e-05	0.00328512	intron-variant	ANKRD13A	GRCh38.p7	12:110012158	TATACTTTTACAATA[A/G]TTTAAAGTCCGTCTG	88455
rs548230072	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110024364	AATGAGTACAGGTAC[C/G]AGTTGTTCTGGTAGG	88455
rs548246081	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110010441	AAGTTCATCGTCTTG[A/T]TACTTTTAAAAAAAT	88455
rs548364893	snp	A/G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110012810	GCCTGCCAGGTCTAC[A/G/T]TATAACCACAGTTAC	88455
rs548387994	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110005329	AAAGATTTTTTTGTA[A/G]AGAAAATGTGTCCCT	88455
rs548427997	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110016166	GCTGCCCAGGCTGGT[C/T]TCAAACTCCTGAGCG	88455
rs548545767	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110036699	AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	88455
rs548564418	snp	A/C/G	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110019680	CCCAGACCACAGAGC[A/C/G]TGGAGTTTCTGGAGG	88455
rs548584303	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110011256	GTGGCTCTGGACACG[C/T]GGTGCAGGTGCCAAA	88455

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