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

ING4

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs14542	snp	C/T	0.0596104	0.162024	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650772	AAAGCAGGAAGGGAA[C/T]GGAGAAGAAAAGTGT	51147
rs2365101	snp	C/T	0.243919	0.249926	intron-variant	ING4	GRCh38.p7	12:6651645	ctcccgagttcaagc[C/T]attctcctgcctcag	51147
rs2365102	snp	C/T	0.251014	0.249998	intron-variant	ING4	GRCh38.p7	12:6651784	tgatctcaagtgatc[C/T]gctcaccttggcctc	51147
rs3809244	snp	A/C	0.258843	0.249844	upstream-variant-2KB	ING4	GRCh38.p7	12:6663709	TGAGAAAGATGATCA[A/C]CTTTCTACTTATAAA	51147
rs3809245	snp	C/T	0.228253	0.249052	upstream-variant-2KB	ING4	GRCh38.p7	12:6664435	TTAGTAAGATAGTAT[C/T]TTAGAGATAGCTGCC	51147
rs4764503	snp	A/G	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6659293	gctagaattacaggc[A/G]tgagccaccgtgcct	51147
rs4764504	snp	A/G	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6659179	CACCTGCCTTCCAGA[A/G]TGCTGGATTACAGGC	51147
rs4764505	snp	A/G	0.0107246	0.0724382	intron-variant	ING4	GRCh38.p7	12:6658962	ATGGGATGAGGAAAA[A/G]CGAGCGGTGCATTCC	51147
rs4764506	snp	A/G	0.0667028	0.170006	intron-variant	ING4	GRCh38.p7	12:6652860	TCTTCATCTGGTGGG[A/G]AGTTTGGCACCAGGT	51147
rs4764615	snp	A/G	0.396	0.202938	intron-variant	ING4	GRCh38.p7	12:6657031	aagtagctgggatta[A/G]agatgcccaccgtca	51147
rs4764616	snp	C/T	0.284733	0.247575	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655665	CAAAAACCCTGGACA[C/T]AGTTCCCTGAGAACT	51147
rs4764617	snp	C/T	0.251859	0.249993	intron-variant	ING4	GRCh38.p7	12:6655326	ccgggtgcggtggct[C/T]acgcctgtaatccca	51147
rs4764618	snp	A/G	0.411074	0.191194	intron-variant	ING4	GRCh38.p7	12:6655192	GTCGGGTGTGGTGGC[A/G]CATGCCAGTAATCCC	51147
rs4764619	snp	C/G	0.251859	0.249993	intron-variant	ING4	GRCh38.p7	12:6654816	AATCCCTTGAACCCA[C/G]GAGGCAGAGGTTGAG	51147
rs5796244	in-del	-/G			intron-variant	ING4	GRCh38.p7	12:6661079	AAGGCTGGGAGCGGT[-/G]GCTCACGCCTATAAT	51147
rs6416323	snp	C/T	0.284995	0.247539	intron-variant	ING4	GRCh38.p7	12:6657480	aaacaaaaaataaaG[C/T]GCAGCTCAGTTTTCC	51147
rs7316048	snp	C/T	0.039522	0.134904	intron-variant	ING4	GRCh38.p7	12:6652106	ctcacgtgatctgcc[C/T]gcctcagcctcccaa	51147
rs7397940	snp	G/T	0.251859	0.249993	intron-variant	ING4	GRCh38.p7	12:6662711	GAGGTCTTTACCGCT[G/T]CTCCAAATGGCAGTG	51147
rs7958346	snp	G/T	0.0471551	0.14613	intron-variant	ING4	GRCh38.p7	12:6659437	gcttaaatccgggag[G/T]tggaggttgcagtga	51147
rs7961940	snp	C/T	0.0577344	0.159793	downstream-variant-500B	ING4	GRCh38.p7	12:6650402	CCCTGGTCTGAGGCC[C/T]ACCCTCCAGCACCTC	51147
rs7962047	snp	C/T	0.0209421	0.100162	downstream-variant-500B	ING4	GRCh38.p7	12:6650513	GCCATCCTCTCACAT[C/T]GCATCCAACCCAGAG	51147
rs7964213	snp	C/T	0.13446	0.221699	intron-variant	ING4	GRCh38.p7	12:6655333	acaggcgtaagccac[C/T]gcacccggccCCAAA	51147
rs7979340	snp	C/G	0.0475351	0.146656	intron-variant	ING4	GRCh38.p7	12:6657329	tggcgggcgcctgta[C/G]tcccagctactcagg	51147
rs7979794	snp	C/T	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6659608	acgaggtcaggagat[C/T]gagaccatcctggct	51147
rs10849494	snp	G/T	0.197531	0.244432	intron-variant	ING4	GRCh38.p7	12:6661414	AGCCTTTGTTTTTTT[G/T]TTTTTTTTTTTTTTT	51147
rs11064301	snp	C/T	0.00517822	0.0506191	downstream-variant-500B	ING4	GRCh38.p7	12:6650479	ACTCTGGTTTCATGT[C/T]GTGTCCTAATTCTGG	51147
rs11064302	snp	G/T	0.00795532	0.062565	intron-variant	ING4	GRCh38.p7	12:6651504	TTTGGAGAATTCTTG[G/T]AAGTCCCAAGGCCAA	51147
rs11064303	snp	A/G	0.0422008	0.138995	intron-variant	ING4	GRCh38.p7	12:6653704	TCCATGTTTGAAGAT[A/G]CTTCTTTGAAGGGCT	51147
rs11064304	snp	A/G	0.0138799	0.0821421	intron-variant	ING4	GRCh38.p7	12:6653992	CTCAGGCACCACCAC[A/G]CCTGGCTAATTTTTT	51147
rs11064305	snp	C/T	0.0130921	0.0798413	intron-variant	ING4	GRCh38.p7	12:6654013	CTAATTTTTTCTATT[C/T]TTTTGTAGAGACAGG	51147
rs11064306	snp	A/C	0.281577	0.247998	intron-variant	ING4	GRCh38.p7	12:6654864	CAAGTAGCTGGGACT[A/C]CAGGTGTGCGCCACC	51147
rs11551179	snp	C/T	0	0	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652971	GAGCTGTCATAGTCA[C/T]TTGACTCAATCTGTT	51147
rs12300751	snp	C/T	0.00557542	0.0525036	intron-variant	ING4	GRCh38.p7	12:6660015	TCTCCCcaggccgaa[C/T]atggctatcatattc	51147
rs12306554	snp	A/T	0.136506	0.222754	intron-variant	ING4	GRCh38.p7	12:6654507	cctgataattttttt[A/T]aaaaaattatttcta	51147
rs12311071	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6661271	cctggctattttttt[A/T]atttttagtagagac	51147
rs12314060	snp	A/G	0.00557542	0.0525036	intron-variant	ING4	GRCh38.p7	12:6660537	cacttgaacccggga[A/G]gcagaggttgcagtg	51147
rs12581338	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6659740	gtggcgtgcatccag[C/G]aggtggagctttcag	51147
rs12825615	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6659734	aggagagtggcgtgc[A/C]tccaggaggtggagc	51147
rs28455167	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6659773	AGCCGAGATCGCTCC[A/T]CTGCACTCCAGCCTG	51147
rs34283927	snp	A/G	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6660146	AAATCTCTTGCCAAG[A/G]CTCCACCTAAAACTT	51147
rs34568819	in-del	-/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6663843	TTTTTTTTTTTTTTT[-/T]GAGACAGAATTTTCA	51147
rs34961465	in-del	-/CT			intron-variant	ING4	GRCh38.p7	12:6662179	ATTCCTTTTTTCTCT[-/CT]CCTCACTGGCAAATA	51147
rs35667235	snp	A/G	0.0711525	0.174681	upstream-variant-2KB	ING4	GRCh38.p7	12:6663748	ATGACTCATAATAAA[A/G]CTATAATTCTGCACA	51147
rs35710003	in-del	-/AA			intron-variant	ING4	GRCh38.p7	12:6659830	AAAAAAAAAAAAAAA[-/AA]TAGATGGGCATGGTG	51147
rs35762960	snp	C/T	0.0785177	0.181917	intron-variant	ING4	GRCh38.p7	12:6660562	GCAGTGGGCCAAGAT[C/T]GCACCATTGCGCTCC	51147
rs35787939	snp	C/T	0.0333695	0.124785	intron-variant	ING4	GRCh38.p7	12:6659685	GGCCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	51147
rs55641348	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6662337	TGTCACAGTGTTTTA[A/T]AATTATTTGCAGAAT	51147
rs55986948	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6662241	GCTGTAAAGCTTTTC[C/T]TACATCCCCAGGTAA	51147
rs58105040	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6658467	CAGGTGGGCGCATCA[C/G]CTGAGCTGAGGAGTT	51147
rs61495500	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6658462	AGGCCCAGGTGGGCG[C/G]ATCAGCTGAGCTGAG	51147
rs74057051	snp	A/G	0.0471551	0.14613	downstream-variant-500B	ING4	GRCh38.p7	12:6650480	CTCTGGTTTCATGTC[A/G]TGTCCTAATTCTGGC	51147
rs74057052	snp	C/T	0.0471551	0.14613	intron-variant	ING4	GRCh38.p7	12:6652167	GTCCAGCCCATCTTT[C/T]TTCTATTCTGAAGTC	51147
rs74057056	snp	C/T	0.078151	0.181571	intron-variant	ING4	GRCh38.p7	12:6662332	TCACTTGTCACAGTG[C/T]TTTATAATTATTTGC	51147
rs74239562	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655340	TRAGCCACCGCACCC[A/G]GCCCCAAATGTTTTA	51147
rs74651259	snp	C/T	0.00835141	0.0640778	intron-variant	ING4	GRCh38.p7	12:6659791	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC	51147
rs74743984	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6655026	CACGGCACCCGGTCT[C/T]CCAGATGTTTTATTT	51147
rs75082820	snp	C/T	0.0126979	0.078662	intron-variant	ING4	GRCh38.p7	12:6660805	GCATGATCTTTTCTC[C/T]GCTGAGTAACTTTCT	51147
rs75155588	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	ING4	GRCh38.p7	12:6664185	TCTCGTGTTTTTGTT[C/T]TCCTTTTGTTTATAT	51147
rs75418571	snp	G/T	0	0	intron-variant	ING4	GRCh38.p7	12:6654345	TCTTTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA	51147
rs76126701	snp	C/T	0.0174175	0.0916809	intron-variant	ING4	GRCh38.p7	12:6662249	GCTTTTCCTACATCC[C/T]CAGGTAATTACCCCC	51147
rs76290581	snp	C/T	0.00874735	0.0655527	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650927	GCACCGACCTCAGCA[C/T]GGAGGCAAAAGGACA	51147
rs76327967	snp	C/T	0.100216	0.200162	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651201	GGCCCTTATCTATTT[C/T]TTCTTCCGTTCTTGG	51147
rs76463160	snp	G/T	0.5	0	intron-variant	ING4	GRCh38.p7	12:6656185	TCTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTTG	51147
rs76592027	snp	A/C	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6658726	CAAAAATAAAAAATG[A/C]AAACCTAATCAAGTC	51147
rs76783851	snp	A/T	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6660129	TCACCCCAGTACAAG[A/T]GAAATCTCTTGCCAA	51147
rs76846620	snp	A/C	0.5	0	intron-variant	ING4	GRCh38.p7	12:6656264	CACTACAACCTCCAC[A/C]TCCCAGGTTCAAACG	51147
rs77114558	snp	A/C	0.5	0	intron-variant	ING4	GRCh38.p7	12:6659814	CGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA	51147
rs77283008	snp	A/G	0.00106447	0.0230456	synonymous-codon, intron-variant, nc-transcript-variant	ING4	GRCh38.p7	12:6652271	CAAAATGTTTCTCAC[A/G]TCAGGGTTGTCACAG	51147
rs77426127	snp	C/T	0.00199481	0.0315187	intron-variant	ING4	GRCh38.p7	12:6662765	ATGGGGAAAAAAATC[C/T]ACCGAGGCTGGAGAC	51147
rs77516085	snp	A/G	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6658957	TAGTTGGAATGCACC[A/G]CTCGCTTTTCCTCAT	51147
rs77742335	in-del	-/T			intron-variant	ING4	GRCh38.p7	12:6661589	ACCATGCCCAGCTAA[-/T]TTTTTTTTTTTTTTA	51147
rs78086878	snp	A/G	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6662484	TGAATAAATGACTCC[A/G]GGCCCTAAAACAAAT	51147
rs78166458	snp	A/T	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6662526	GAGCAATAGGCTTTC[A/T]GCAGGGGTGGTTTAC	51147
rs78194930	snp	A/C	0.0376037	0.131863	upstream-variant-2KB	ING4	GRCh38.p7	12:6663321	TTTTGCATGGTAGCC[A/C]CGACCGCCCACAGTG	51147
rs78635226	snp	G/T	0.5	0	intron-variant	ING4	GRCh38.p7	12:6656186	CTTTTTTTTTTTTTT[G/T]GAGACAGAGTCTTGC	51147
rs79526248	snp	A/T	0.5	0	intron-variant	ING4	GRCh38.p7	12:6659830	AAAAAAAAAAAAAAA[A/T]TAGATGGGCATGGTG	51147
rs79655322	snp	A/G	0.0437281	0.141251	intron-variant	ING4	GRCh38.p7	12:6660233	GGGAGGCCAAGGCAG[A/G]TAGATCGCTTGATCT	51147
rs79682518	snp	A/G	0.0498117	0.149749	intron-variant	ING4	GRCh38.p7	12:6654475	GTAGCTGGGACCACA[A/G]GCACATGCCACTACA	51147
rs79906574	snp	G/T	0.5	0	intron-variant	ING4	GRCh38.p7	12:6656187	TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT	51147
rs79942815	snp	A/C/T	0.0741367	0.177809	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655642	CTGGTTCTCACCATT[A/C/T]GGCAGGCAGTTCTCA	51147
rs80101392	snp	A/C	0.5	0	intron-variant	ING4	GRCh38.p7	12:6659812	AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	51147
rs80223260	snp	A/G	0.5	0	downstream-variant-500B	ING4	GRCh38.p7	12:6650264	AAAGGAAAAAAAAAA[A/G]GAAGTCAAGCTAATG	51147
rs111594180	snp	A/C	0.5	0	downstream-variant-500B	ING4	GRCh38.p7	12:6650429	CCTCTGTCTTTCCCA[A/C]GTTGAGAACTTACAA	51147
rs111933102	snp	C/G	0.00517822	0.0506191	intron-variant	ING4	GRCh38.p7	12:6659010	GCCTATTAAATTCCT[C/G]TTCGTTCTTCCAAAG	51147
rs112500523	in-del	-/A	0.5	0	downstream-variant-500B	ING4	GRCh38.p7	12:6650254	ACTTCGCCTCAAAGG[-/A]AAAAAAAAAAGAAGT	51147
rs112505199	snp	A/G	0.5	0	intron-variant	ING4	GRCh38.p7	12:6653548	CTGTGCCATGCACTC[A/G]AGTAATGGAACATAC	51147
rs112962175	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6656345	CACACCTGGCTAGTT[C/T]TTGTATTTTTAGTAG	51147
rs113711890	snp	C/G	0	0	splice-acceptor-variant, intron-variant	ING4	GRCh38.p7	12:6652419	CCATACTCAGGACTT[C/G]TGCATGCCAAGAGGA	51147
rs113932069	snp	A/C	0.5	0	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652668	ATCACTCACGTGCGC[A/C]CGAGCTTTAACTTCT	51147
rs114082659	snp	C/G	0.0182019	0.0936463	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650828	GAGGGGGAATGAAGA[C/G]GTCTGGGGGACTGCC	51147
rs114423275	snp	A/G	0.00398564	0.0444627	intron-variant	ING4	GRCh38.p7	12:6654143	TGCCTGGCCTAATCT[A/G]TTTATTTTTAGAGGC	51147
rs114905789	snp	A/T	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655782	CATGGCTACATAGAA[A/T]GAAGACAAGACTACA	51147
rs114937023	snp	G/T	0.0209421	0.100162	upstream-variant-2KB	ING4	GRCh38.p7	12:6665008	AAAAGCAGTAAATAT[G/T]CAGGGAGCTAAGAAA	51147
rs115021376	snp	C/G	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6651985	TCGCCTCAGCCTCCC[C/G]AGTAGCTGGGATGAC	51147
rs115151324	snp	A/T	0.00676609	0.0577691	intron-variant	ING4	GRCh38.p7	12:6662321	TTTCCATTATCTCAC[A/T]TGTCACAGTGTTTTA	51147
rs115808834	snp	A/G	0.0368353	0.130617	intron-variant	ING4	GRCh38.p7	12:6653800	TCTGCCGCAAATCAG[A/G]CTGAGTCATCTGCTG	51147
rs115876538	snp	A/T	0.0387552	0.1337	intron-variant	ING4	GRCh38.p7	12:6655056	TTATTTTATTTATTT[A/T]TTTTTGAGACCAAGT	51147
rs116142617	snp	C/G	0.0368353	0.130617	intron-variant	ING4	GRCh38.p7	12:6651897	TGCTCTTGTCGCCCA[C/G]GTTAGAGTGTGGTGG	51147
rs116416840	snp	A/G	0.00199481	0.0315187	intron-variant	ING4	GRCh38.p7	12:6655389	TGTCCCAGGACATTG[A/G]GACTATAGATGTTTA	51147
rs116693623	snp	C/T	0.00358779	0.0422022	intron-variant	ING4	GRCh38.p7	12:6652139	TGCTGGGATTTCAGG[C/T]AAGAGCTACTACGTC	51147
rs116778327	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655684	CCAGGGTTTTTGATG[A/G]TGTTCACCTTTTCAT	51147
rs117012163	snp	A/G	0.0277256	0.114429	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6652727	CGAGTTTTTCCCTTT[A/G]GAACGAGCACGAGCA	51147
rs117458578	snp	A/G	0.00953873	0.0683987	intron-variant	ING4	GRCh38.p7	12:6660478	GCTGGGTATGGTGGC[A/G]GGCACTGTAATCCTA	51147
rs117962564	snp	C/T	0.0512789	0.15169	intron-variant	ING4	GRCh38.p7	12:6656823	AGAGAGAAACAATCA[C/T]AGGACTGACTATGCA	51147
rs118133042	snp	C/G	0.0376037	0.131863	intron-variant	ING4	GRCh38.p7	12:6662910	GATCCTGCTGCCCCG[C/G]CCCCTCTTTCTCCGC	51147
rs138320021	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658333	CTCCTGGTATCCTCT[A/G]TTATACACATAACAC	51147
rs138380307	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664997	GAGTGGGAGGAAAAA[A/G]CAGTAAATATGCAGG	51147
rs138434482	snp	C/G	0.00914312	0.0669923	intron-variant	ING4	GRCh38.p7	12:6661371	AAAGTGTTGGGATTA[C/G]AGGCATGAGCCACCG	51147
rs138530648	snp	C/G	0.0471551	0.14613	intron-variant	ING4	GRCh38.p7	12:6654349	TTTTTTTTTTTTTGA[C/G]ACAGGGTCTCACTCT	51147
rs139075674	snp	C/T	1.64741e-05	0.00286998	missense, synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6651355	TGGTTGTCAGCCCCA[C/T]ACAGGCAAAATGGAA	51147
rs139096775	snp	C/T	0.0023933	0.0345097	intron-variant	ING4	GRCh38.p7	12:6659538	AAAAATTAGGCCAGG[C/T]GCGGTGGCTCACACC	51147
rs139114422	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661860	AAATCAGGTTCTTAT[A/C]TCTGTCCTGGAATGT	51147
rs139185675	snp	A/G	0.000693458	0.0186077	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653334	CCAATTTTTCCTCGG[A/G]GCTCAGGCTGCGGGC	51147
rs139374084	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656095	ACAATGAGAGAAGTA[C/G]AAACATTCTAGTCAT	51147
rs139677673	snp	C/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6663651	GTCTGAATTTCTATT[C/G]ACTCACACAAACACC	51147
rs140242201	snp	A/G	0.00874735	0.0655527	downstream-variant-500B	ING4	GRCh38.p7	12:6650182	CTTGAACCCGGAGGC[A/G]GAGACTGCAGTGAGC	51147
rs140339044	snp	A/G	0.000153988	0.00877328	synonymous-codon, missense, nc-transcript-variant	ING4	GRCh38.p7	12:6651377	AAAATGGAACCACTC[A/G]ATGGAACACTGGAAG	51147
rs140626685	in-del	-/CCCC			upstream-variant-2KB	ING4	GRCh38.p7	12:6663268	GCCCTTACTATATTA[-/CCCC]CCGCCGGTACACATC	51147
rs140970573	snp	C/G	3.2962e-05	0.00405954	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6656760	GGTCCCTCATGAGCT[C/G]AAAGTTTCTCTGTAA	51147
rs140974549	snp	A/G	1.67379e-05	0.00289287	intron-variant	ING4	GRCh38.p7	12:6652469	GGAAGGGAAGCTAAA[A/G]CCTGAGGCTTTCAGA	51147
rs141004604	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664362	GGGTATGAGAGGCTG[C/T]CAACACACTAGGCTG	51147
rs141345063	snp	A/G/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6665001	GGGAGGAAAAAGCAG[A/G/T]AAATATGCAGGGAGC	51147
rs141585612	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661467	CTGTCACCCAGGCTG[C/G]AGTGCAGTGGTATGT	51147
rs141593131	snp	A/G	0.0170251	0.090679	intron-variant	ING4	GRCh38.p7	12:6661032	CTCCTGACCTAAGGC[A/G]ATCCACCCATCTCAG	51147
rs141623263	snp	A/C	0.0520825	0.152737	intron-variant	ING4	GRCh38.p7	12:6660513	CTCAAGAGGCTGAGG[A/C]AGGAGAATCACTTGA	51147
rs141655303	snp	C/T	0.00318978	0.0398085	intron-variant	ING4	GRCh38.p7	12:6659461	GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTTC	51147
rs141682293	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6657601	ATTTCTGCATGGCTA[G/T]CCCACCCTTTTCGCC	51147
rs141975388	snp	A/G	0.0524604	0.153226	intron-variant	ING4	GRCh38.p7	12:6658643	GTGAGCCGAGATCAC[A/G]CCAATGCACTCCAGC	51147
rs142232044	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	ING4	GRCh38.p7	12:6663192	GGCTAAAGCCTTTCC[A/G]CCCTTAAAAGGAGAA	51147
rs142380796	snp	A/G	4.94588e-05	0.00497262	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652662	CCCTGAATCACTCAC[A/G]TGCGCACGAGCTTTA	51147
rs142996541	snp	C/T	0.00318978	0.0398085	intron-variant	ING4	GRCh38.p7	12:6653901	AGGGTCTCACTTTGT[C/T]GCCCAGGCTGGAGTG	51147
rs143139704	snp	A/G	0.0185938	0.0946107	intron-variant	ING4	GRCh38.p7	12:6655334	CAGGCGTAAGCCACC[A/G]CACCCGGCCCCAAAT	51147
rs143157442	snp	A/G	0.0471551	0.14613	intron-variant	ING4	GRCh38.p7	12:6657404	CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA	51147
rs143202414	snp	A/G	6.61244e-05	0.0057496	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663075	CTTACTGTCCAGATA[A/G]TGTTCCAAATACATC	51147
rs143207314	snp	C/T	0.00835141	0.0640778	intron-variant	ING4	GRCh38.p7	12:6651891	GAGTCTTGCTCTTGT[C/T]GCCCAGGTTAGAGTG	51147
rs143261067	snp	C/T	0.0329836	0.124112	intron-variant	ING4	GRCh38.p7	12:6660921	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG	51147
rs143542983	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652151	AGGCAAGAGCTACTA[C/T]GTCCAGCCCATCTTT	51147
rs143895274	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662264	CCAGGTAATTACCCC[C/G]CTTTTCTCCAGGGTT	51147
rs144116100	snp	A/G	0.00993419	0.0697739	intron-variant	ING4	GRCh38.p7	12:6654400	TGCAGTGGCATGATC[A/G]TGGATCACACTGCAG	51147
rs144340616	snp	A/G	0.000977395	0.0220849	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653348	GAGCTCAGGCTGCGG[A/G]CACTACTCATATACT	51147
rs144975797	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6656322	CTGGGATTACTGGTG[C/T]GTGCCACCACACCTG	51147
rs145124387	snp	C/G	0.000798403	0.0199641			GRCh38.p7	12:6665144	CTTTATTTATCCCAG[C/G]CCAACTACATAACAA	51147
rs145532274	snp	A/G	0.0123036	0.0774623	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650768	GAAAAAAGCAGGAAG[A/G]GAATGGAGAAGAAAA	51147
rs145716079	snp	C/T	0.00835141	0.0640778	upstream-variant-2KB	ING4	GRCh38.p7	12:6664533	TAAAGAGACAGACTT[C/T]CAGCTATATAATTTC	51147
rs145758074	snp	C/T	0.00438332	0.0466095	intron-variant	ING4	GRCh38.p7	12:6661248	GACTACAGGGGCACA[C/T]CACCACACCTGGCTA	51147
rs145897632	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	ING4	GRCh38.p7	12:6664549	CAGCTATATAATTTC[C/T]ACCAAATATGTGGAG	51147
rs146174641	snp	A/G	0.00874735	0.0655527	intron-variant	ING4	GRCh38.p7	12:6659462	CAGTGAGCTGAGATC[A/G]CACCACTGCACTTCA	51147
rs146215840	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6661832	AACTCCTAAATACTT[C/G]TGTAACTCCCTAAAA	51147
rs146347929	snp	A/G	0.00112102	0.0236485	synonymous-codon, intron-variant	ING4	GRCh38.p7	12:6652397	GCCAAAGGTCACTGA[A/G]GGCATCCCATACTCA	51147
rs146754766	snp	C/T	0.00874735	0.0655527	intron-variant	ING4	GRCh38.p7	12:6651980	GCCTCTCGCCTCAGC[C/T]TCCCGAGTAGCTGGG	51147
rs147027287	snp	A/G	0.0437281	0.141251	intron-variant	ING4	GRCh38.p7	12:6657801	CAGGTGTGGTGGCAC[A/G]TACCTGTAATCCCAG	51147
rs147393279	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663373	GCCCTTACAGACACC[A/C]CAGGACGCGACCGAG	51147
rs147464807	snp	C/T	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6653960	CTCAACTTCCTGAGC[C/T]CTGGTGATCCTCCCA	51147
rs147493061	snp	C/T	1.65384e-05	0.00287557	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663093	TTCCAAATACATCCC[C/T]GCAGCCATCTCGAAG	51147
rs147534183	snp	C/T	0.00716266	0.059414	downstream-variant-500B	ING4	GRCh38.p7	12:6650181	ACTTGAACCCGGAGG[C/T]GGAGACTGCAGTGAG	51147
rs147657525	snp	C/G	0.0166325	0.0896639	intron-variant	ING4	GRCh38.p7	12:6660621	TCAAAAACAAACAAA[C/G]AAACAGAAAAACTAA	51147
rs147692225	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6664063	CGGTGAGGCTGGTCT[C/T]GAACTTCCGACCTCA	51147
rs147828273	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660352	GGTGGCTCATGCCTG[C/T]AATCCCAGCACTCTG	51147
rs147897876	snp	A/G	0.00318978	0.0398085	intron-variant	ING4	GRCh38.p7	12:6657481	AACAAAAAATAAAGT[A/G]CAGCTCAGTTTTCCT	51147
rs148370559	snp	C/T	0.0162398	0.0886349	intron-variant	ING4	GRCh38.p7	12:6661000	GTTTCACTATGTTAG[C/T]CAGGCTGGTCTTGGA	51147
rs148498382	in-del	-/TAAC	0.0150606	0.0854603	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655714	TGTGTAAACTCAGAG[-/TAAC]TTAAGACACAGCTTC	51147
rs148681796	snp	C/T	0.0192222	0.0961332	intron-variant	ING4	GRCh38.p7	12:6663043	TCTGCAGCCCCGACC[C/T]CCACCTCCAGCCTGC	51147
rs148999703	snp	A/G	0.021333	0.101051	upstream-variant-2KB	ING4	GRCh38.p7	12:6664541	CAGACTTTCAGCTAT[A/G]TAATTTCTACCAAAT	51147
rs149019207	in-del	-/TTTCT			intron-variant	ING4	GRCh38.p7	12:6660816	TCTCCGCTGAGTAAC[-/TTTCT]TTTCTTTTCTTTTGA	51147
rs149136396	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660877	GCTGGAGTGCAATGG[C/T]GCAATCTCAGGTTCA	51147
rs149402439	snp	A/G	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6659275	AATACAAAAATTAGG[A/G]CCAGGCACGGTGGCT	51147
rs149452261	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661899	ATTGATCTCTGTTAT[C/G]AACAATATCATGCTC	51147
rs149630308	snp	C/T	8.23716e-05	0.00641709	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652731	TTTTTCCCTTTGGAA[C/T]GAGCACGAGCAGCTT	51147
rs149715276	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6660269	GTCTGAGACCAGCCT[A/G]GGCAATATGGCCAGA	51147
rs149767033	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB	ING4	GRCh38.p7	12:6664430	TGGTGTTAGTAAGAT[A/G]GTATTTTAGAGATAG	51147
rs149962987	snp	C/G/T	0.00438332	0.0466095	intron-variant	ING4	GRCh38.p7	12:6656167	TTGACTTTCTTTAAT[C/G/T]CTTCTTTTTTTTTTT	51147
rs150080565	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652702	GGGCAGTCTTGGGGG[C/T]TTCTTCATCCGAGTT	51147
rs150219696	snp	A/G	1.64855e-05	0.00287097	intron-variant	ING4	GRCh38.p7	12:6652774	GAGTCCGGCCTTCTA[A/G]GGAAGAGGGAGAAAG	51147
rs150274000	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658673	CCTGGATGACAGAGC[A/C]AGACACTGACTCAAA	51147
rs150675992	snp	A/T	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650804	GATCACACCTAGCCC[A/T]CACCACAGGAGGGGG	51147
rs180868921	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6660325	ATATATAAAAAATAA[A/G]AGGCCTGGTACGGTG	51147
rs180952713	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	ING4	GRCh38.p7	12:6650340	GGAAATTAAGTGAAA[C/G]ATGTTTTATGGAGAA	51147
rs181258937	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6661885	GAATGTTATCACTAA[C/T]TGATCTCTGTTATCA	51147
rs181348751	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656539	TTTTCACAATACTCT[A/G]TTTGTTATGAAAAAG	51147
rs181755622	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654039	ACAGGCTTTTTCCAC[A/G]TTACCCAGGCTGGTC	51147
rs181802517	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6657828	CCAGCTATTCAGGAG[G/T]CTGAGGCAGGAGAAT	51147
rs182129497	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659191	GCACTCTGGAAGGCA[A/G]GTGGATCACTCAAGG	51147
rs182295432	snp	C/T	0.00318978	0.0398085	intron-variant	ING4	GRCh38.p7	12:6655491	AGATAACCAGGAGGA[C/T]CTGTGAAGACACTGT	51147
rs182374020	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663180	AAGCCATTTTGCGGC[C/T]AAAGCCTTTCCGCCC	51147
rs182456249	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6651761	TGGCCAGGCCAGTCT[C/T]GAACTCCTGATCTCA	51147
rs182868868	snp	A/G	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6662795	CCCTGGAGAATGGGG[A/G]CAGCAACTATCTTCC	51147
rs183236100	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	ING4	GRCh38.p7	12:6664582	GAGGAACTTCCAACC[C/T]GGGGCGGATTGGAAG	51147
rs183344440	snp	G/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6658369	ATCTACTTCCATATA[G/T]TAGCCAGAATGTCCT	51147
rs183469034	snp	C/T	0.00597247	0.0543191	intron-variant	ING4	GRCh38.p7	12:6652217	TTTTCCCTCTTGTAC[C/T]CACTCCCTTCATGCC	51147
rs183488268	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6657219	CTTTGGGAGGCCGAG[A/G]AGAGCAGATCACGAG	51147
rs183903268	snp	C/T	0.00159617	0.0282053	intron-variant	ING4	GRCh38.p7	12:6652572	CTTGGCGCAGACATA[C/T]AGAAAGCGGCAGGGG	51147
rs184192704	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664995	GAGAGTGGGAGGAAA[A/C]AGCAGTAAATATGCA	51147
rs184691998	snp	C/T	0.00199481	0.0315187	intron-variant	ING4	GRCh38.p7	12:6660193	TGCTGGGCACAGTGG[C/T]TCACGCCTGTAATCC	51147
rs184942338	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650892	AAGGAGAATGAAAAG[G/T]ACCCTCCCTCTGAAA	51147
rs185148566	snp	C/G	0.00279162	0.0372561	intron-variant	ING4	GRCh38.p7	12:6654559	GCCCAGGCTGGTCTT[C/G]AACTCCTGGTCAAAT	51147
rs185205811	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6656232	GGAGTGCAGTGACAT[A/G]TGGCATGATTTGGGC	51147
rs185281709	snp	A/C	0.00159617	0.0282053	intron-variant	ING4	GRCh38.p7	12:6659793	ACTCCAGCCTGGGCG[A/C]CAGAGCGAGACTCTG	51147
rs185477072	snp	A/G	0.0023933	0.0345097	intron-variant	ING4	GRCh38.p7	12:6656618	GTAAAAAAGGAGCGA[A/G]AGAAGCCACAGTTCT	51147
rs185938364	snp	A/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660654	TAAAATAAATAAAAA[A/T]AAATAAAATGCCTCT	51147
rs186138742	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6660515	CAAGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC	51147
rs186470750	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6662823	TCCTGGCCATGCACA[C/T]TAGCCCTTCAAGACA	51147
rs186742663	snp	C/T	9.88728e-05	0.00703041	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652669	TCACTCACGTGCGCA[C/T]GAGCTTTAACTTCTT	51147
rs186951244	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662411	GTCTTACTCATTTTT[C/G]TATCCCTAGTGCCTG	51147
rs186978620	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6658402	TTAAAAAATGCAAAC[C/T]TGGCCAGGCACGGTG	51147
rs187211536	snp	A/C	0.0205511	0.0992634	downstream-variant-500B	ING4	GRCh38.p7	12:6650088	GAAACCCTGTCTCTA[A/C]TAAAAATACAAAATT	51147
rs187533426	snp	A/C	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6652119	CCCGCCTCAGCCTCC[A/C]AAAGTGCTGGGATTT	51147
rs187781804	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663437	CATTCTCTAGCAAAC[C/T]TTTTTCCCTCCAAAA	51147
rs188045176	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659636	GCTAACATGGTGAAA[C/T]CCCGTCTCTACTAAA	51147
rs188538581	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6657475	CAAACAAACAAAAAA[G/T]AAAGTGCAGCTCAGT	51147
rs188559850	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	ING4	GRCh38.p7	12:6664801	AAACTGCTCTAATTA[C/T]AAAAGTCATGCTTTT	51147
rs188803082	snp	A/C	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6652474	GGAAGCTAAAGCCTG[A/C]GGCTTTCAGAGGTGG	51147
rs189139509	snp	A/C	0.00199481	0.0315187	intron-variant	ING4	GRCh38.p7	12:6660262	CTCAGGAGTCTGAGA[A/C]CAGCCTGGGCAATAT	51147
rs189376160	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6665116	CAGGATATCTAGCAC[C/T]AAATTAAGTGGGCTT	51147
rs189659029	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660771	AAGCCTATCCTAAAA[A/C]ATATCTCTGCAGCAG	51147
rs189671832	snp	A/T	0.00279162	0.0372561	intron-variant	ING4	GRCh38.p7	12:6653692	AGTGTATTTTTGTCC[A/T]TGTTTGAAGATGCTT	51147
rs189674781	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656453	GTGCTGGGATTACAG[C/G]TGTGAGCCAGCCTGG	51147
rs190178177	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6659942	GCAAAAGAGCAAGAC[G/T]GTTTCAAAAAACAAA	51147
rs190241985	snp	A/G	0.000395348	0.0140541	intron-variant	ING4	GRCh38.p7	12:6651285	GGGAGAATGCCCTTG[A/G]CCACTCAACTTAGGG	51147
rs190900185	snp	C/T	1.65332e-05	0.00287512	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663087	ATAATGTTCCAAATA[C/T]ATCCCCGCAGCCATC	51147
rs191255034	snp	A/T	1.64768e-05	0.00287021	intron-variant	ING4	GRCh38.p7	12:6656683	AGAAAAATAAATGAT[A/T]ACACACACTCATTAG	51147
rs191447389	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658750	TCAAGTCACTCTCCC[A/G]CTTATAACCTTCTGG	51147
rs191547692	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6652216	ATTTTCCCTCTTGTA[C/T]CCACTCCCTTCATGC	51147
rs191847714	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662681	GCCACTTTTGAGGAA[G/T]AATGGAGTGGAGGAG	51147
rs191924892	snp	A/G	3.314e-05	0.00407049	intron-variant	ING4	GRCh38.p7	12:6653209	TGGGAAGTAGGTGGG[A/G]AGCCATGAACAGGGC	51147
rs192086409	snp	A/G	0.0138799	0.0821421	intron-variant	ING4	GRCh38.p7	12:6657885	CAGTGAGCCAAGACT[A/G]CACTACTGCACTCCA	51147
rs192096461	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	ING4	GRCh38.p7	12:6650288	GCTAATGTATAGTAT[A/G]GCAGTACGTATGTAT	51147
rs192103725	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	ING4	GRCh38.p7	12:6664827	CTTTTCGGTAACTTG[A/C]TCTCTGTGCCTGTTT	51147
rs192773045	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663618	GGGAAGAGTATCAGG[A/C/T]CTTGAGACATTTAAA	51147
rs192858028	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659737	AGAGTGGCGTGCATC[C/T]AGGAGGTGGAGCTTT	51147
rs193216862	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652571	TCTTGGCGCAGACAT[A/G]TAGAAAGCGGCAGGG	51147
rs193921122	snp	A/C			missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653001	TCAAG[A/C]	51147
rs199557258	snp	A/G	0.0004813	0.0155054	intron-variant	ING4	GRCh38.p7	12:6656812	ACCTAGGGAAGAGAG[A/G]GAAACAATCACAGGA	51147
rs199584457	in-del	-/T	0.202035	0.245356	intron-variant	ING4	GRCh38.p7	12:6655052	ATTTTATTTTATTTA[-/T]TTTTTTTTTGAGACC	51147
rs199755461	in-del	-/T			intron-variant	ING4	GRCh38.p7	12:6656186	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC	51147
rs199768855	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663117	CTCGAAGCAAAACAA[A/G]GCAACTTCCGATCCG	51147
rs199800012	snp	A/G	1.64844e-05	0.00287087	missense, utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651209	TCTATTTCTTCTTCC[A/G]TTCTTGGGAGCAGCG	51147
rs200091123	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6651410	GAAGAAAGAAGTAGT[C/T]AGGGGCCAGGAAGGG	51147
rs200352672	snp	A/G	1.65748e-05	0.00287874	intron-variant	ING4	GRCh38.p7	12:6656804	TTTTCAATACCTAGG[A/G]AAGAGAGAGAAACAA	51147
rs200797875	in-del	-/AG	0.0119091	0.0762411	upstream-variant-2KB	ING4	GRCh38.p7	12:6663747	AATGACTCATAATAA[-/AG]CTATAATTCTGCACA	51147
rs201193156	snp	A/C	0.000891383	0.0210926	intron-variant	ING4	GRCh38.p7	12:6652806	CAGAAGGCAGGGAGA[A/C]AGAAAGATGGGTTAA	51147
rs201257362	snp	C/T	1.65696e-05	0.00287828	missense, intron-variant, nc-transcript-variant	ING4	GRCh38.p7	12:6652279	TTCTCACATCAGGGT[C/T]GTCACAGCCAATCAT	51147
rs201343501	snp	A/C	0.000551272	0.0165931	upstream-variant-2KB	ING4	GRCh38.p7	12:6663151	CGGAAGTGACTGTAA[A/C]GCGACAGGGGCCGAA	51147
rs201583077	in-del	-/T			intron-variant	ING4	GRCh38.p7	12:6656172	TTTCTTTAATTCTTC[-/T]TTTTTTTTTTTTTTG	51147
rs201626425	snp	C/T	4.94214e-05	0.00497074	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6652712	GGGGGCTTCTTCATC[C/T]GAGTTTTTCCCTTTG	51147
rs201702577	snp	A/G	4.98981e-05	0.00499465	intron-variant	ING4	GRCh38.p7	12:6651429	GGCCAGGAAGGGCCA[A/G]AGGAAGGAGAGAAAG	51147
rs201814087	in-del	-/A			intron-variant	ING4	GRCh38.p7	12:6660648	TAAAATAAAATAAAT[-/A]AAAAAAAAATAAAAT	51147
rs201828515	in-del	-/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6663846	TGCCCTCTTGCTTTT[-/G]TTTTTTTTTTTTTTG	51147
rs201959427	snp	G/T	0.00199792	0.0315431	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653323	TTTGAGAAGGGCCAA[G/T]TTTTCCTCGGAGCTC	51147
rs202244844	in-del	-/AT			upstream-variant-2KB	ING4	GRCh38.p7	12:6663743	AAAGAATGACTCATA[-/AT]AAAGCTATAATTCTG	51147
rs367938103	snp	A/C	0.000153988	0.00877328	upstream-variant-2KB	ING4	GRCh38.p7	12:6663149	CCCGGAAGTGACTGT[A/C]ACGCGACAGGGGCCG	51147
rs368139819	snp	A/C/T	6.6386e-05	0.00576101	intron-variant	ING4	GRCh38.p7	12:6653096	ACAAAACTATCTCCA[A/C/T]TTAAAGAAAATAGGT	51147
rs368282932	snp	A/G	0.0023933	0.0345097	intron-variant	ING4	GRCh38.p7	12:6657381	ATGAACCTGGGAGGC[A/G]GAGTTTGCAGTGAGC	51147
rs368401528	snp	C/G	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6661397	CACCGTGCCTGGCCA[C/G]CAGCCTTTGTTTTTT	51147
rs368831542	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6660981	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTATGT	51147
rs369007352	snp	A/C	0.000153988	0.00877328	missense, intron-variant, splice-acceptor-variant	ING4	GRCh38.p7	12:6652310	CTCTCCATAGGAGAC[A/C]TGGTGACAAAGGCAA	51147
rs369074922	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6657071	AGGCATGAGAATCAC[C/T]TGAATCCAGGAGGCA	51147
rs369078014	in-del	-/C			intron-variant	ING4	GRCh38.p7	12:6652928	TCACAGCCCCGCCCC[-/C]TCCTCACTCTTTTTG	51147
rs369199001	snp	A/C/T	1.69974e-05	0.0029152	intron-variant	ING4	GRCh38.p7	12:6652241	TCATGCCCCTCACAA[A/C/T]CCCCCATCCTAAGGC	51147
rs369340158	snp	C/G	4.99073e-05	0.00499511	intron-variant	ING4	GRCh38.p7	12:6656821	AGAGAGAGAAACAAT[C/G]ACAGGACTGACTATG	51147
rs369382813	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6656242	GACATGTGGCATGAT[G/T]TGGGCTCACTACAAC	51147
rs369429695	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6662839	TAGCCCTTCAAGACA[A/C]GTCTCTAACCCCCAC	51147
rs369627731	snp	A/G	1.64765e-05	0.00287019	intron-variant	ING4	GRCh38.p7	12:6656688	AATAAATGATTACAC[A/G]CACTCATTAGATACA	51147
rs369960359	snp	A/T	0.000193981	0.00984647	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651143	ATTCCTCTGCCCACT[A/T]GCCCAAGTCAGGGGA	51147
rs369982495	snp	C/G	0.00358779	0.0422022	upstream-variant-2KB	ING4	GRCh38.p7	12:6664142	AACCACTGTGCCTGG[C/G]CCCTCTTGCTACTCT	51147
rs370066441	snp	G/T	1.66827e-05	0.00288809	intron-variant	ING4	GRCh38.p7	12:6652460	TCATCTACAGGAAGG[G/T]AAGCTAAAGCCTGAG	51147
rs370186769	snp	C/T	4.96849e-05	0.00498397	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6663050	CCCCGACCCCCACCT[C/T]CAGCCTGCTCTTACT	51147
rs370290467	snp	A/G	0.00279162	0.0372561	intron-variant	ING4	GRCh38.p7	12:6653791	CAGCAGTTGTCTGCC[A/G]CAAATCAGGCTGAGT	51147
rs370306437	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6660544	ACCCGGGAGGCAGAG[A/G]TTGCAGTGGGCCAAG	51147
rs370725040	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6659804	GGCGACAGAGCGAGA[A/C]TCTGTCTCAAAAAAA	51147
rs370864194	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6659660	TACTAAAAATACAAA[A/C]AAATTAGCTGGCCGT	51147
rs371079611	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6654409	ATGATCATGGATCAC[A/G]CTGCAGCCTCAACCT	51147
rs371095155	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652737	CCTTTGGAACGAGCA[C/T]GAGCAGCTTTCTTCT	51147
rs371180258	snp	A/T	1.65302e-05	0.00287486	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663073	CTCTTACTGTCCAGA[A/T]AATGTTCCAAATACA	51147
rs371595694	snp	C/T	6.62438e-05	0.00575478	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653345	TCGGAGCTCAGGCTG[C/T]GGGCACTACTCATAT	51147
rs371654809	snp	A/C	1.65061e-05	0.00287277	synonymous-codon, intron-variant	ING4	GRCh38.p7	12:6652403	GGTCACTGAGGGCAT[A/C]CCATACTCAGGACTT	51147
rs371782306	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6662549	TGGTTTACATAAATC[A/G]CATAAACACCAGATT	51147
rs371902029	snp	A/G	8.24042e-05	0.00641836	synonymous-codon, missense, nc-transcript-variant	ING4	GRCh38.p7	12:6651380	ATGGAACCACTCAAT[A/G]GAACACTGGAAGAGG	51147
rs371999289	snp	A/G	3.30972e-05	0.00406786	intron-variant	ING4	GRCh38.p7	12:6651413	GAAAGAAGTAGTCAG[A/G]GGCCAGGAAGGGCCA	51147
rs372015955	snp	A/G	1.6552e-05	0.00287676	intron-variant	ING4	GRCh38.p7	12:6652917	CGCCCCACCTCTCAC[A/G]GCCCCGCCCCCTCCT	51147
rs372047897	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6655958	TTGTCAATTACTGCT[G/T]TTTTTTCTTTCCTCT	51147
rs372107980	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6656438	CCTAGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	51147
rs372474150	in-del	-/AAG			upstream-variant-2KB	ING4	GRCh38.p7	12:6663746	GAATGACTCATAATA[-/AAG]CTATAATTCTGCACA	51147
rs372623035	snp	A/G	0.000307953	0.0124049	intron-variant	ING4	GRCh38.p7	12:6653414	ACAACAGAGACAGAG[A/G]CCTGGTCACAATGGC	51147
rs372703606	in-del	-/A			intron-variant	ING4	GRCh38.p7	12:6660316	ATTAAATATATATAT[-/A]AAAAAATAAAAGGCC	51147
rs372723521	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663184	CATTTTGCGGCTAAA[C/G]CCTTTCCGCCCTTAA	51147
rs372890189	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6656616	GCGTAAAAAAGGAGC[A/G]AGAGAAGCCACAGTT	51147
rs373029305	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6657322	GGTGCGATGGCGGGC[A/G]CCTGTACTCCCAGCT	51147
rs373140860	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651123	CCCCTGGCCCCAGCA[C/T]AGGCATTCCTCTGCC	51147
rs373285320	snp	C/T	4.94287e-05	0.00497111	intron-variant	ING4	GRCh38.p7	12:6656689	ATAAATGATTACACA[C/T]ACTCATTAGATACAA	51147
rs373315687	in-del	-/AACT			intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655715	GTGTAAACTCAGAGT[-/AACT]TAAGACACAGCTTCA	51147
rs374088120	snp	C/G/T	3.31439e-05	0.00407073	intron-variant	ING4	GRCh38.p7	12:6652613	CTGGGAGTGGGGCAC[C/G/T]GGGAGAGAAGAGGAT	51147
rs374164160	in-del	-/CTTTT			intron-variant	ING4	GRCh38.p7	12:6660829	ACTTTCTTTTCTTTT[-/CTTTT]GAGGTGTAGTGTCGC	51147
rs374302902	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6658123	CGCCACCACACCCGA[A/C]TAATTTTTGTATTTT	51147
rs374376796	snp	A/T	6.60186e-05	0.00574499	intron-variant	ING4	GRCh38.p7	12:6651403	GGAAGAGGAAGAAAG[A/T]AGTAGTCAGGGGCCA	51147
rs374390006	snp	A/G	0.000133123	0.00815742	utr-variant-5-prime, upstream-variant-2KB	ING4	GRCh38.p7	12:6663137	CTTCCGATCCGCCCC[A/G]GAAGTGACTGTAACG	51147
rs374519072	snp	C/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6663842	TGCCTTGCCCTCTTG[C/G]TTTTTTTTTTTTTTT	51147
rs374543463	snp	C/T	4.94817e-05	0.00497377	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652965	CTGGAAGAGCTGTCA[C/T]AGTCACTTGACTCAA	51147
rs374663258	snp	C/T	3.29652e-05	0.00405974	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652764	TTCTCCTTTTGAGTC[C/T]GGCCTTCTAGGGAAG	51147
rs374943107	in-del	-/T			intron-variant	ING4	GRCh38.p7	12:6661105	GCCTTTTTGTTTTTG[-/T]TTTTTTTTTTGAGGC	51147
rs375077387	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6654907	TTTTTGCATTTTTAG[C/T]AGAGATGTGGTTTCA	51147
rs375094296	snp	A/G	0.000437904	0.0147905	intron-variant	ING4	GRCh38.p7	12:6662989	TCGTCACTGGAACTT[A/G]AGGGCTACAGATCCT	51147
rs375300631	snp	C/T	0.000153988	0.00877328	intron-variant	ING4	GRCh38.p7	12:6652246	CCCCTCACAACCCCC[C/T]ATCCTAAGGCAAAAT	51147
rs375319936	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6661249	ACTACAGGGGCACAC[A/C]ACCACACCTGGCTAT	51147
rs375724899	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6659341	CGGGTGGCTCACTTG[A/G]AGCCAGGAGTTCAAG	51147
rs375883182	snp	A/G	0.000153988	0.00877328	intron-variant	ING4	GRCh38.p7	12:6653439	AATGGCCCCTGAGTG[A/G]CTAGGTGAAACACAT	51147
rs376107723	snp	C/T	0.000153988	0.00877328	intron-variant	ING4	GRCh38.p7	12:6656691	AAATGATTACACACA[C/T]TCATTAGATACAAAA	51147
rs376569778	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	ING4	GRCh38.p7	12:6650175	AGAATCACTTGAACC[C/T]GGAGGCGGAGACTGC	51147
rs376640690	snp	C/G			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650728	TAGGGCCAGAGCCTA[C/G]ATGACCTGGTGGATC	51147
rs376814511	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6662582	CATTTGATGGGAATT[A/C]GATCTTTACTCCATG	51147
rs376965069	snp	A/T	1.65353e-05	0.00287531	missense, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6663065	CCAGCCTGCTCTTAC[A/T]GTCCAGATAATGTTC	51147
rs377231817	snp	C/G	1.65905e-05	0.0028801	intron-variant	ING4	GRCh38.p7	12:6652432	TTCTGCATGCCAAGA[C/G]GAAGAGAAAGTGTCA	51147
rs377491922	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6658424	GGCACGGTGGCTCAT[A/G]CCTGTAATCCCAGCA	51147
rs377602366	in-del	-/T			intron-variant	ING4	GRCh38.p7	12:6656347	CACCTGGCTAGTTTT[-/T]GTATTTTTAGTAGAG	51147
rs377653085	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6659398	TGTAATCCCAGATAC[C/T]TGGGAGGCTGAGGCA	51147
rs377698152	in-del	-/A			upstream-variant-2KB	ING4	GRCh38.p7	12:6663222	ACTTCCGCCCTTAAA[-/A]GGAGAACTTCCGCCC	51147
rs377703421	snp	C/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6664003	GTATGCACCATCACG[C/G]CAGACTAATTTTGTA	51147
rs397850551	in-del	-/T			intron-variant	ING4	GRCh38.p7	12:6661115	TTTTGTTTTTTTTTT[-/T]GAGGCGGAGTCTCAC	51147
rs527311142	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6665076	TATTACACAACATAT[C/T]GAGACACCATCTTAG	51147
rs527425427	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658796	CTGAAGATGTTCTGC[A/G]CTTTCTGGCCCTTGC	51147
rs527552409	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6658348	ATTATACACATAACA[C/T]TTCCAATCTACTTCC	51147
rs527615549	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6661111	TTTGTTTTTGTTTTT[G/T]TTTTGAGGCGGAGTC	51147
rs527882212	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659502	ACAGAGTGCGACTCC[A/G]TCTCAAAAACAAAAC	51147
rs528422950	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6661031	ACTCCTGACCTAAGG[C/T]GATCCACCCATCTCA	51147
rs528440943	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652680	CGCACGAGCTTTAAC[C/T]TCTTCTGGGCAGTCT	51147
rs528563625	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662909	CGATCCTGCTGCCCC[A/G]CCCCCTCTTTCTCCG	51147
rs529093085	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655673	GGGAACTGTGTCCAG[A/G]GTTTTTGATGATGTT	51147
rs529175298	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6658022	TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG	51147
rs529252360	snp	A/G	3.30759e-05	0.00406655	intron-variant	ING4	GRCh38.p7	12:6653084	GAAAGGAGAGGTACA[A/G]AACTATCTCCAATTA	51147
rs529375876	snp	A/C			upstream-variant-2KB	ING4	GRCh38.p7	12:6664626	CTTCGAGATGGATGC[A/C]GGGATGTATTTGAAA	51147
rs529664055	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	ING4	GRCh38.p7	12:6650092	CCCTGTCTCTACTAA[A/T]AATACAAAATTAGCT	51147
rs529778229	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659562	TCACACCTGTAATCC[C/T]GGCACTTTGGGTGGC	51147
rs530244176	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652580	AGACATATAGAAAGC[A/G]GCAGGGGGCGGTGCA	51147
rs530640172	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6661106	GCCTTTTTGTTTTTG[G/T]TTTTTTTTTGAGGCG	51147
rs530818654	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6653902	GGGTCTCACTTTGTC[A/G]CCCAGGCTGGAGTGC	51147
rs530874411	snp	C/T	0.00538679	0.0516176	intron-variant	ING4	GRCh38.p7	12:6655956	CATTGTCAATTACTG[C/T]TTTTTTTTCTTTCCT	51147
rs530904962	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6659266	TCTACTAAAAATACA[A/G]AAATTAGGGCCAGGC	51147
rs530931962	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663558	TTTTTTTCCCTCTTT[C/T]GCAGAATGACTTTTT	51147
rs531274267	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662919	GCCCCGCCCCCTCTT[C/T]CTCCGCACCCTCCAA	51147
rs531348336	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6665027	GGAGCTAAGAAACAT[A/T]GGCATATTTGGTCAT	51147
rs531527662	snp	C/T	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6658106	CTGGGACCACAGGCG[C/T]GCGCCACCACACCCG	51147
rs531667128	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6655297	GACTCACCCGCCTCT[A/G]CCTCCCAAAGTGCTG	51147
rs531792795	snp	A/G	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6657772	CTGTTTCTACTAAAA[A/G]TATAAAAATTAGCCA	51147
rs531813572	in-del	-/C	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6661450	GGACACGGAGTCTTT[-/C]TCTGTCACCCAGGCT	51147
rs531875502	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650853	ACTGCCCCCATGCTA[C/T]GCCCCAGTCCTTAAA	51147
rs532195741	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652630	GGAGAGAAGAGGATG[C/T]CATCCGGCAAAGGGC	51147
rs532268419	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6657408	GAGCCGAGATCGCAC[C/T]ACTGCACTCCAGCCT	51147
rs532507813	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662005	TTAAAAGACCTTGTC[C/T]AATCTAGCCTCAGCC	51147
rs533026599	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655280	AACTCCTTATCTCAG[A/G]AGACTCACCCGCCTC	51147
rs533163024	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661622	GTAGAGACTGGGCTT[C/T]ACCATGTTGGACAGG	51147
rs533366846	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656654	TCATACCAGATGATA[C/T]GGTAACATCAAGTAG	51147
rs533445447	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6654878	TACAGGTGTGCGCCA[A/C]CACATCTGGCTAATT	51147
rs533495612	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650612	GTATAGCTTTTATTT[A/G]CCTACCCAAGTTCCT	51147
rs533565597	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6657312	AAATTAGCCAGGTGC[G/T]ATGGCGGGCGCCTGT	51147
rs533625180	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	ING4	GRCh38.p7	12:6650314	TGTATAGCACAAATA[C/T]ATCATTTATTGGAAA	51147
rs533627190	snp	C/T	0.0154538	0.0865337	intron-variant	ING4	GRCh38.p7	12:6657897	ACTGCACTACTGCAC[C/T]CCAGCCTGGTGACAG	51147
rs533686415	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650956	CAGTGGGCAAGACCA[C/T]GTCCCTCCGAAGGGA	51147
rs533711801	snp	C/T	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6656128	TATAAATATATCAAA[C/T]GTGGAGAGCAGAAAT	51147
rs533720561	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664443	ATAGTATTTTAGAGA[G/T]AGCTGCCACCCCTCA	51147
rs533844175	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664058	CATGTCGGTGAGGCT[C/G]GTCTCGAACTTCCGA	51147
rs534197148	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6655621	CTGTATTACAAAAAA[A/G]GCAATCTGGTTCTCA	51147
rs534646708	snp	C/T	0.00159617	0.0282053	intron-variant	ING4	GRCh38.p7	12:6662764	TATGGGGAAAAAAAT[C/T]TACCGAGGCTGGAGA	51147
rs534776606	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654747	TTTTTTGTTTTGAGA[C/T]GGAGTCACGCTCTGT	51147
rs534831857	snp	A/G	0.00199481	0.0315187	intron-variant	ING4	GRCh38.p7	12:6652012	TGACAGTCGTGTGCC[A/G]CTATGCTCAGCTAAT	51147
rs534992709	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6660296	CAGATCCTGTCTCTA[C/T]AAAAATTAAATATAT	51147
rs535321052	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660878	CTGGAGTGCAATGGC[A/G]CAATCTCAGGTTCAA	51147
rs535951385	snp	A/G	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6651892	AGTCTTGCTCTTGTC[A/G]CCCAGGTTAGAGTGT	51147
rs536070643	snp	A/G	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6656228	GGCTGGAGTGCAGTG[A/G]CATGTGGCATGATTT	51147
rs536153276	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6657332	CGGGCGCCTGTACTC[C/T]CAGCTACTCAGGAGG	51147
rs536193417	in-del	-/A	0.00358779	0.0422022	upstream-variant-2KB	ING4	GRCh38.p7	12:6663219	AGAACTTCCGCCCTT[-/A]AAAGGAGAACTTCCG	51147
rs536202701	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658108	GGGACCACAGGCGCG[C/T]GCCACCACACCCGAC	51147
rs536387406	snp	A/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660649	TAAAATAAAATAAAT[A/T]AAAAAAAATAAAATG	51147
rs536407343	snp	A/C	9.98885e-05	0.00706642	intron-variant	ING4	GRCh38.p7	12:6652451	GAGAAAGTGTCATCT[A/C]CAGGAAGGGAAGCTA	51147
rs536484451	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB	ING4	GRCh38.p7	12:6664665	GGACAGTAAGAGCAG[G/T]CTGGAGGAGGGGGTT	51147
rs536729217	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659925	TAGAGGTTGCAGCCC[A/G]GGCAAAAGAGCAAGA	51147
rs536793678	snp	A/G	0.000815735	0.0201793	intron-variant	ING4	GRCh38.p7	12:6652453	GAAAGTGTCATCTAC[A/G]GGAAGGGAAGCTAAA	51147
rs536820235	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6661626	AGACTGGGCTTCACC[A/G]TGTTGGACAGGGTGA	51147
rs537399684	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	ING4	GRCh38.p7	12:6663288	CGGTACACATCCGCC[C/T]GACACTGAAACTTTT	51147
rs537466586	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	ING4	GRCh38.p7	12:6663937	GCAACCTCCACCTCC[C/T]GGGTTCAAGTGATTC	51147
rs537518552	snp	C/T	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6656287	TTCAAACGATTCTCA[C/T]GTCTCAGCCTCCCAA	51147
rs537659631	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661422	TTTTTTTTTTTTTTT[G/T]TTTTTTTGAGAGGGA	51147
rs538723212	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661201	CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTTAG	51147
rs538725505	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652881	CAGATGAAGAGCTGA[A/C]TTCTTCTCCCTTTCA	51147
rs538911173	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659096	GGTATTCTAGCCACC[G/T]TTTTAAAGCACTTAT	51147
rs538967076	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6651972	ATTCTCCTGCCTCTC[A/G]CCTCAGCCTCCCGAG	51147
rs539511355	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6656229	GCTGGAGTGCAGTGA[C/T]ATGTGGCATGATTTG	51147
rs539801369	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656348	ACCTGGCTAGTTTTT[A/G]TATTTTTAGTAGAGA	51147
rs539835353	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6659327	TTGGGAGGCCGAGGC[A/G]GGTGGCTCACTTGAA	51147
rs539994043	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6655036	GGTCTCCCAGATGTT[C/T]TATTTTATTTTATTT	51147
rs540028640	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662849	AGACACGTCTCTAAC[C/G]CCCACACCGCACCCC	51147
rs540059232	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654977	TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTACT	51147
rs540068601	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655321	AGTGCTGGGATTACA[A/G]GCGTAAGCCACCGCA	51147
rs540116312	snp	A/G	0.00159617	0.0282053	intron-variant	ING4	GRCh38.p7	12:6655408	TATAGATGTTTACTA[A/G]TATTTGGAAGGGCTC	51147
rs540124946	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6657807	TGGTGGCACGTACCT[A/G]TAATCCCAGCTATTC	51147
rs540226596	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6657215	AGCACTTTGGGAGGC[C/T]GAGGAGAGCAGATCA	51147
rs540590602	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664944	TCTAATACTGGTGAT[A/G]AAGTTAGGGCCATTA	51147
rs540716646	snp	A/G			downstream-variant-500B	ING4	GRCh38.p7	12:6650112	CAAAATTAGCTGGGC[A/G]TGGTAGCATGTGCCT	51147
rs540730418	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650764	CCATGAAAAAAGCAG[C/G]AAGGGAATGGAGAAG	51147
rs540924333	in-del	-/A	0.0520825	0.152737	intron-variant	ING4	GRCh38.p7	12:6660315	ATTAAATATATATAT[-/A]AAAAAATAAAAGGCC	51147
rs541355785	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664039	AGTAGAGATGGGGTT[C/T]CTCCATGTCGGTGAG	51147
rs541927911	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6663349	GTGAGGCGGCTGTAG[C/T]CCGCTTCCGCCCTTA	51147
rs542070830	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6661022	GGTCTTGGAACTCCT[A/G]ACCTAAGGCGATCCA	51147
rs542673219	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659359	CCAGGAGTTCAAGAC[C/G]AGCCTGGCCAACATG	51147
rs543230097	in-del	-/A	0.339882	0.233284	intron-variant	ING4	GRCh38.p7	12:6659813	GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	51147
rs543532060	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660280	GCCTGGGCAATATGG[C/T]CAGATCCTGTCTCTA	51147
rs543816447	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655186	GTAGCTGGGATTACT[A/G]GCATGCGCCACCACA	51147
rs543951410	snp	C/G	0.00199481	0.0315187	intron-variant	ING4	GRCh38.p7	12:6652597	CAGGGGGCGGTGCAG[C/G]CTGGGAGTGGGGCAC	51147
rs544345345	snp	A/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6663658	TTTCTATTCACTCAC[A/G]CAAACACCATCTCCC	51147
rs544708125	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664817	AAAAGTCATGCTTTT[C/G]GGTAACTTGATCTCT	51147
rs545205151	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	ING4	GRCh38.p7	12:6650507	TGGCATGCCATCCTC[A/T]CACATTGCATCCAAC	51147
rs545909628	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6653756	TCAAAAGCCATTGTT[C/T]CCTTCTCAAAAACAT	51147
rs546379320	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6654355	TTTTTTTGAGACAGG[G/T]TCTCACTCTATTGCC	51147
rs546984224	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664466	ACCCCTCACACTTTT[C/T]GTACCCTCACACATC	51147
rs547007979	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6664048	GGGGTTTCTCCATGT[C/T]GGTGAGGCTGGTCTC	51147
rs547053253	snp	C/T	0.00159617	0.0282053	downstream-variant-500B	ING4	GRCh38.p7	12:6650085	GGTGAAACCCTGTCT[C/T]TACTAAAAATACAAA	51147
rs547184382	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6658899	CTGCCTCAAACTGGC[C/T]TGTGCTCCTCCTGCC	51147
rs547217263	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663701	TTTTAACTTGAGAAA[A/G]ATGATCACCTTTCTA	51147
rs547327639	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656148	AGAGCAGAAATGACT[C/T]GAGTTGACTTTCTTT	51147
rs547344500	snp	C/T	0.0119091	0.0762411	intron-variant	ING4	GRCh38.p7	12:6653703	GTCCATGTTTGAAGA[C/T]GCTTCTTTGAAGGGC	51147
rs547351477	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6661273	TGGCTATTTTTTTTA[G/T]TTTTAGTAGAGACGG	51147
rs547397891	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6657983	TTTGTTTTTTGAGAC[A/G]GAGTCTGGCTCTGTT	51147
rs547557798	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6651788	CTCAAGTGATCTGCT[C/T]ACCTTGGCCTCCCAA	51147
rs547620171	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652120	CCGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTTC	51147
rs548114285	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660601	TGACAGAGTGAGACT[C/G]TGTCTCAAAAACAAA	51147
rs548245441	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6654726	TAGATATTGCTCCAA[A/G]CACGTTTTTTTGTTT	51147
rs548256486	snp	A/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662269	TAATTACCCCCCTTT[A/T]CTCCAGGGTTGCCTA	51147
rs548319098	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654749	TTTTGTTTTGAGACG[G/T]AGTCACGCTCTGTTG	51147
rs548366665	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6658153	TTAGTAGACACAGGG[G/T]TTCACCATTTTGGCC	51147
rs549063021	snp	A/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6664752	CCCAGGTTTACTAGT[A/G]TGCAGGTAGTAAGAT	51147
rs549404718	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6657596	TTTCCATTTCTGCAT[A/G]GCTATCCCACCCTTT	51147
rs549585031	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656980	CAACATGGCGAGACC[G/T]CCATCTCTATTAAAA	51147
rs549640242	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	ING4	GRCh38.p7	12:6650168	AGGCAGGAGAATCAC[C/T]TGAACCCGGAGGCGG	51147
rs549711034	snp	A/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6664877	TACCTCCCTCATAGG[A/G]TTGTTGGAATAAGTG	51147
rs549713893	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658964	AATGCACCGCTCGCT[C/T]TTCCTCATCCCATCC	51147
rs549722684	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6661840	AATACTTCTGTAACT[A/C]CCTAAAATCAGGTTC	51147
rs550003369	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6659540	AAATTAGGCCAGGCG[C/T]GGTGGCTCACACCTG	51147
rs550325482	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661155	CAGGCTGGAGTGCAG[G/T]GGCATGATCTCGGCC	51147
rs550530970	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6653903	GGTCTCACTTTGTCG[C/G]CCAGGCTGGAGTGCA	51147
rs550844265	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654497	GCCACTACACCCTGA[C/T]AATTTTTTTAAAAAA	51147
rs550959958	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	ING4	GRCh38.p7	12:6663565	CCCTCTTTTGCAGAA[C/T]GACTTTTTTCAAGCC	51147
rs551010976	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664558	AATTTCTACCAAATA[C/T]GTGGAGAAGAGGAAC	51147
rs551071905	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6665046	ATATTTGGTCATATG[G/T]GATACATTCATTGGT	51147
rs551072243	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6657176	AACAAATGGCCAGGC[A/G]TGGTGGCTCACACCT	51147
rs551305981	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662967	CCGCTTCATAATTGT[A/G]ACCTTCTCGTCACTG	51147
rs551321139	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6655024	GCCACGGCACCCGGT[A/C]TCCCAGATGTTTTAT	51147
rs551783439	snp	C/T	0.00159617	0.0282053	intron-variant	ING4	GRCh38.p7	12:6651695	TACAGGCACAGGCTA[C/T]CATGCCTGGCTAATT	51147
rs551906151	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6664901	ATAAGTGAGTGTGAG[C/T]GTATCCATAAAAAGA	51147
rs552044671	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6653216	TAGGTGGGGAGCCAT[G/T]AACAGGGCCATACCA	51147
rs552234281	snp	A/C/G	0.000148701	0.00862149	intron-variant	ING4	GRCh38.p7	12:6652636	AAGAGGATGTCATCC[A/C/G]GCAAAGGGCTCCCTG	51147
rs552364981	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6655204	ATGCGCCACCACACC[C/T]GACTAATTTTTGTAT	51147
rs552512402	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659654	CGTCTCTACTAAAAA[C/T]ACAAAAAAATTAGCT	51147
rs552646669	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662102	GAGTCATAAATATCA[A/G]ACACCCTTGACCTTG	51147
rs552735138	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661749	TCACTTTCTAAGCAG[A/G]AAGAAGCCACCTTAG	51147
rs553382920	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6661161	GGAGTGCAGTGGCAT[G/T]ATCTCGGCCCACTGC	51147
rs553455477	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6657318	GCCAGGTGCGATGGC[A/G]GGCGCCTGTACTCCC	51147
rs553589516	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654986	CGCCTCGGCCTCCCA[A/G]AGTACTGGGATTACA	51147
rs553650271	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655445	ATGTCAGTAGTAAGA[C/G]ACAAGTCTGACTCTA	51147
rs553787353	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664583	AGGAACTTCCAACCC[A/G]GGGCGGATTGGAAGT	51147
rs553836718	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6655633	AAAAGCAATCTGGTT[C/G]TCACCATTCGGCAGG	51147
rs553848260	in-del	-/T	0.0154538	0.0865337	intron-variant	ING4	GRCh38.p7	12:6656343	ACCACACCTGGCTAG[-/T]TTTTGTATTTTTAGT	51147
rs553975394	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664122	GTGCTGGGATTACAG[A/G]TGCGAACCACTGTGC	51147
rs553980455	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659283	AATTAGGGCCAGGCA[C/T]GGTGGCTCATGCCTG	51147
rs554182295	snp	A/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658571	CATGCCTGTAATCCC[A/T]GCTACTTGGGAGGCT	51147
rs554233530	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6654241	TCTTTTCGCCTCCTG[A/T]GTAGTTGAGTATATC	51147
rs554768341	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652015	CAGTCGTGTGCCACT[A/G]TGCTCAGCTAATTTT	51147
rs554902596	snp	A/G	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6660888	ATGGCGCAATCTCAG[A/G]TTCAAGGAATTCTTG	51147
rs554911881	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654056	TACCCAGGCTGGTCT[C/T]GAACTCCTGGGTCAA	51147
rs554970073	snp	A/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6653632	AGTTGGAATTTAAAT[A/T]ACTGAAACACAGCAA	51147
rs555444944	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655585	CAACTGTCTTTCCAT[A/G]CATGAACTCAAGAGT	51147
rs555649977	snp	A/C	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6656254	GATTTGGGCTCACTA[A/C]AACCTCCACCTCCCA	51147
rs555705689	snp	A/G	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6661969	ATACTCTACTTTAAA[A/G]TGCAAACTTCTTCGT	51147
rs555853414	snp	C/G	0.00164614	0.028642	intron-variant	ING4	GRCh38.p7	12:6651307	AACTTAGGGACCCTC[C/G]AACTCCTGCCACTTA	51147
rs556185267	snp	A/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659964	AAAAACAAAAAAATT[A/T]AAAAAAATAATGTGT	51147
rs556186631	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658202	TGGCCTCAGGTGATC[C/T]GCCCGCCTTGATCTC	51147
rs556371479	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664674	GAGCAGGCTGGAGGA[A/G]GGGGTTCAGGGGCTG	51147
rs556391067	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652463	TCTACAGGAAGGGAA[A/G]CTAAAGCCTGAGGCT	51147
rs556748428	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6656247	GTGGCATGATTTGGG[A/C]TCACTACAACCTCCA	51147
rs556758756	in-del	-/CT			intron-variant	ING4	GRCh38.p7	12:6656201	TGAGACAGAGTCTTG[-/CT]CTGTTGCCTAGGCTG	51147
rs557317329	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654172	GCAGGCGCAGGTTCT[A/C]TCTTATGTTTGTTGC	51147
rs557318141	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663938	CAACCTCCACCTCCC[A/G]GGTTCAAGTGATTCT	51147
rs557375369	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656309	GCCTCCCAAGTAGCT[A/G]GGATTACTGGTGCGT	51147
rs557570174	in-del	-/C	0.00517822	0.0506191	intron-variant	ING4	GRCh38.p7	12:6658025	GTGCAGTGGCACGAT[-/C]CTTGGCTCACTGCAG	51147
rs557575235	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6661445	GAGAGGGACACGGAG[C/T]CTTTCTCTGTCACCC	51147
rs558513493	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652547	AGATACCAAAATGAT[A/C]AGAAGAGTTCTTGGC	51147
rs558838969	snp	A/G	1.64893e-05	0.0028713	intron-variant	ING4	GRCh38.p7	12:6651391	CAATGGAACACTGGA[A/G]GAGGAAGAAAGAAGT	51147
rs559280785	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6661012	TAGCCAGGCTGGTCT[C/T]GGAACTCCTGACCTA	51147
rs559394542	in-del	-/T	0.0023933	0.0345097	upstream-variant-2KB	ING4	GRCh38.p7	12:6663765	ATAATTCTGCACATC[-/T]TTTTGTCAGAGCTCC	51147
rs559430129	snp	A/G	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6653781	AAACATCCCACAGCA[A/G]TTGTCTGCCGCAAAT	51147
rs559493431	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654337	TCTATTTTTCTTTTT[C/T]TTTTTTTTTGAGACA	51147
rs559815945	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662893	CCCATCAGCGGGGCC[C/T]CGATCCTGCTGCCCC	51147
rs559878084	snp	C/T	0.00636936	0.0560724	intron-variant	ING4	GRCh38.p7	12:6654069	CTCGAACTCCTGGGT[C/T]AAGCAATCTGCCTGC	51147
rs559890628	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655324	GCTGGGATTACAGGC[A/G]TAAGCCACCGCACCC	51147
rs559953875	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655671	CAGGGAACTGTGTCC[A/G]GGGTTTTTGATGATG	51147
rs560069380	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663389	CAGGACGCGACCGAG[A/G]CAGGTATGACGTCAC	51147
rs560552707	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650691	AATCCTCTTGGCACA[A/G]AGGAAGGGGTGCCCC	51147
rs560789782	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664478	TTTCGTACCCTCACA[C/T]ATCCTTCATAAGAAT	51147
rs560833714	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659541	AATTAGGCCAGGCGC[A/G]GTGGCTCACACCTGT	51147
rs561126850	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652130	CTCCCAAAGTGCTGG[A/G]ATTTCAGGCAAGAGC	51147
rs561570645	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655153	GGTTCAAGCGATTCT[C/T]CTGCATCAGCCTCCT	51147
rs561669753	in-del	-/CT	0.00358779	0.0422022	downstream-variant-500B	ING4	GRCh38.p7	12:6650079	CAACACGGTGAAACC[-/CT]GTCTCTACTAAAAAT	51147
rs561703941	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654457	CCCATTTCAGCCTCT[A/G]GAGTAGCTGGGACCA	51147
rs561787210	snp	C/T	0.00159617	0.0282053	intron-variant	ING4	GRCh38.p7	12:6661069	AATGTGCTAGGATTA[C/T]AGGCGTGAGCCACCG	51147
rs561828931	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6661053	CCCATCTCAGCCTCC[A/C]AATGTGCTAGGATTA	51147
rs561968356	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6658177	TTTGGCCAGACTGGT[C/G]TTGAACTCCTGGCCT	51147
rs562016475	snp	A/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6652047	GTATTTTTAGTAGAG[A/T]AGGGGTTACACTATG	51147
rs562123937	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663502	TTCACTTTAGGCTCA[C/T]ATTGCGTAAACATAC	51147
rs562522327	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656538	GTTTTCACAATACTC[C/T]ATTTGTTATGAAAAA	51147
rs562720396	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6658104	AGCTGGGACCACAGG[C/T]GCGCGCCACCACACC	51147
rs562723698	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6651635	CAACCCCCGCCTCCC[A/G]AGTTCAAGCTATTCT	51147
rs562948490	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652052	TTTAGTAGAGAAGGG[G/T]TTACACTATGTTGGC	51147
rs563159087	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6657629	GCCTTCAGTGACCTT[C/T]CTTTATAAATAAGCT	51147
rs563208394	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650947	GCAAAAGGACAGTGG[A/G]CAAGACCACGTCCCT	51147
rs563258102	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652607	TGCAGGCTGGGAGTG[A/G]GGCACCGGGAGAGAA	51147
rs563327699	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6664587	ACTTCCAACCCGGGG[C/T]GGATTGGAAGTTGCT	51147
rs563396698	snp	A/C	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6660943	GATTACAGGCGTCTG[A/C]CACCACGCCCAGCTA	51147
rs563881455	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6657764	GTGAAAGCCTGTTTC[C/T]ACTAAAAATATAAAA	51147
rs563934428	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6661989	AACTTCTTCGTTTGG[C/T]TTAAAAGACCTTGTC	51147
rs564000547	snp	A/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6654506	CCCTGATAATTTTTT[A/T]AAAAAAATTATTTCT	51147
rs564231065	snp	C/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6664173	CTAAGGGGGAAATCT[C/G]GTGTTTTTGTTTTCC	51147
rs564481645	in-del	-/T	0.296364	0.245663	upstream-variant-2KB	ING4	GRCh38.p7	12:6663843	GCCTTGCCCTCTTGC[-/T]TTTTTTTTTTTTTTT	51147
rs564533134	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656625	AGGAGCGAGAGAAGC[C/T]ACAGTTCTCCAGATC	51147
rs564590791	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6657427	GCACTCCAGCCTGGG[C/T]GACACAGTGAGACTC	51147
rs564803882	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663578	AATGACTTTTTTCAA[C/G]CCAGTTAGTTTCTTA	51147
rs565115868	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658751	CAAGTCACTCTCCCG[A/C]TTATAACCTTCTGGT	51147
rs565259800	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652107	TCACGTGATCTGCCC[A/G]CCTCAGCCTCCCAAA	51147
rs565849323	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654652	TGCCCATCCTATTTG[G/T]CTCATCATTGCAACT	51147
rs565883087	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6654224	GTCCTCAAGTGATTC[C/T]ATCTTTTCGCCTCCT	51147
rs565994242	snp	C/T	1.70127e-05	0.00291652	intron-variant	ING4	GRCh38.p7	12:6652234	ACTCCCTTCATGCCC[C/T]TCACAACCCCCCATC	51147
rs566053819	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661288	TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTA	51147
rs566305746	snp	A/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6664798	GGGAAACTGCTCTAA[A/T]TACAAAAGTCATGCT	51147
rs566316124	in-del	-/A	0.00398564	0.0444627	upstream-variant-2KB	ING4	GRCh38.p7	12:6663239	AGAACTTCCGCCCTT[-/A]AAAGGAGAACTTCCG	51147
rs566941082	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663702	TTTAACTTGAGAAAG[A/G]TGATCACCTTTCTAC	51147
rs567062686	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655482	TGCAGCAACAGATAA[C/T]CAGGAGGATCTGTGA	51147
rs567524383	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	ING4	GRCh38.p7	12:6664659	TTATCTGGACAGTAA[A/G]AGCAGGCTGGAGGAG	51147
rs567529220	snp	C/G	0.0119091	0.0762411	intron-variant	ING4	GRCh38.p7	12:6662360	TGCAGAATCTGTTTC[C/G]TACTAGATCGTGAGC	51147
rs568437419	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654788	GGTGTGCAGTGGCAC[A/G]ATCTTGGCTCACCTC	51147
rs568462602	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662914	CTGCTGCCCCGCCCC[C/T]TCTTTCTCCGCACCC	51147
rs568581451	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663825	TATAAAATATTACTT[C/T]CTGCCTTGCCCTCTT	51147
rs568635460	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661404	CCTGGCCACCAGCCT[C/T]TGTTTTTTTTTTTTT	51147
rs568647137	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664548	TCAGCTATATAATTT[C/G]TACCAAATATGTGGA	51147
rs568944624	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6655238	TAGCAGAGACAGGGT[G/T]TCACCATATGGGCCA	51147
rs568970600	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656270	AACCTCCACCTCCCA[G/T]GTTCAAACGATTCTC	51147
rs569548472	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6651948	ACCTCTGCCTCCTAG[A/G]TTCAAGCAATTCTCC	51147
rs569662453	snp	A/G	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6659627	ACCATCCTGGCTAAC[A/G]TGGTGAAACCCCGTC	51147
rs569785620	snp	A/G	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6660686	CTGTTTAAACCTACA[A/G]CTTCAGGTCTGCTAC	51147
rs569818025	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6662225	TTCAAACATCACCTC[C/T]GCTGTAAAGCTTTTC	51147
rs569848200	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661167	CAGTGGCATGATCTC[A/G]GCCCACTGCAACCTC	51147
rs569849091	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6656092	TTAACAATGAGAGAA[A/G]TAGAAACATTCTAGT	51147
rs570624306	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6653926	GGAGTGCAGTGGCAC[A/G]ATCATGGCTCACTGC	51147
rs570715137	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6659315	AATTCTAGCACTTTG[G/T]GAGGCCGAGGCGGGT	51147
rs570964008	snp	A/G	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6657216	GCACTTTGGGAGGCC[A/G]AGGAGAGCAGATCAC	51147
rs571146894	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	ING4	GRCh38.p7	12:6664562	TCTACCAAATATGTG[A/G]AGAAGAGGAACTTCC	51147
rs571195993	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655397	GACATTGAGACTATA[C/G]ATGTTTACTAATATT	51147
rs571274739	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6665058	ATGTGATACATTCAT[C/T]GGTATTACACAACAT	51147
rs572142213	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6663921	GTGATCATGGCTCAC[C/T]GCAACCTCCACCTCC	51147
rs572363194	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6657135	CTCCAGCCTGGGCAA[C/T]AGAGCAAGTCCCTGT	51147
rs572420797	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6660272	TGAGACCAGCCTGGG[C/T]AATATGGCCAGATCC	51147
rs572435286	snp	A/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652569	GTTCTTGGCGCAGAC[A/T]TATAGAAAGCGGCAG	51147
rs572664239	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660169	TAAAACTTTAAAAAT[A/G]CCTCTACTTGCTGGG	51147
rs572806404	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6661756	CTAAGCAGGAAGAAG[C/T]CACCTTAGATTCTTC	51147
rs572817082	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6662575	AGATTTTCATTTGAT[A/G]GGAATTAGATCTTTA	51147
rs573002781	snp	A/T	0.00159617	0.0282053	intron-variant	ING4	GRCh38.p7	12:6655052	TATTTTATTTTATTT[A/T]TTTTTTTTTGAGACC	51147
rs573298843	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	ING4	GRCh38.p7	12:6650392	TTTGGAGACCCCCTG[G/T]TCTGAGGCCTACCCT	51147
rs573334327	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663411	TGACGTCACTGGAGG[G/T]CGCCATTTTGCATTC	51147
rs573825625	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6656448	CCAAAGTGCTGGGAT[G/T]ACAGGTGTGAGCCAG	51147
rs573962392	snp	A/G	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6658590	ACTTGGGAGGCTGGG[A/G]CACAAAAATCCCTTG	51147
rs574111239	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6652025	CCACTATGCTCAGCT[A/C]ATTTTTGTATTTTTA	51147
rs574152402	snp	G/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6651491	TTTACTCCATCCTTT[G/T]GGAGAATTCTTGGAA	51147
rs574899213	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	ING4	GRCh38.p7	12:6663223	CTTCCGCCCTTAAAA[A/G]GAGAACTTCCGCCCT	51147
rs574988944	snp	A/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660920	GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG	51147
rs575045780	snp	C/T	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6653666	ATCCTTTGCACACCA[C/T]ATTAATATGAAGTGT	51147
rs575206253	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6655164	TTCTCCTGCATCAGC[A/C]TCCTGAGTAGCTGGG	51147
rs575223967	snp	A/G	0.00159617	0.0282053	intron-variant	ING4	GRCh38.p7	12:6655616	TACAACTGTATTACA[A/G]AAAAAGCAATCTGGT	51147
rs575402385	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6657102	GAGGTTGCAGTGAGC[C/T]GTGATTGAGCCACTG	51147
rs575793092	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664375	TGCCAACACACTAGG[C/T]TGTCAACACACTGCC	51147
rs575914028	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6660430	CCTGGCCAACACAGT[A/G]AAACCTCATCTCTAC	51147
rs576091501	in-del	-/T	0.0119091	0.0762411	upstream-variant-2KB	ING4	GRCh38.p7	12:6663744	AAGAATGACTCATAA[-/T]AAAGCTATAATTCTG	51147
rs576162618	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6660821	GCTGAGTAACTTTCT[C/T]TTCTTTTCTTTTGAG	51147
rs576165396	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6657403	GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC	51147
rs576205796	snp	A/C/G	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6656422	TCAAGTTACCTGCCC[A/C/G]CCTAGGCCTCCCAAA	51147
rs576322582	snp	C/G	9.88386e-05	0.00702919	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651341	TTTCCCCCGAGGCTT[C/G]GTTGTCAGCCCCACA	51147
rs576348340	snp	A/T	0.00279162	0.0372561	intron-variant	ING4	GRCh38.p7	12:6652060	AGAAGGGGTTACACT[A/T]TGTTGGCCAGGCTGG	51147
rs576357723	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6659448	GGAGGTGGAGGTTGC[A/C]GTGAGCTGAGATCGC	51147
rs576375272	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658254	CATGAGCCACTAAGA[C/T]GGGCCCCTTTCTTTT	51147
rs576761146	in-del	-/C	0.00517822	0.0506191	intron-variant	ING4	GRCh38.p7	12:6660600	TGACAGAGTGAGACT[-/C]CTGTCTCAAAAACAA	51147
rs576980782	snp	C/G	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6660979	TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACTAT	51147
rs577230471	snp	A/G	0.00119737	0.0244387	intron-variant	ING4	GRCh38.p7	12:6654325	CTTACTGCTCACTCT[A/G]TTTTTCTTTTTTTTT	51147
rs577484071	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6663335	CACGACCGCCCACAG[G/T]GAGGCGGCTGTAGCC	51147
rs577502250	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6654232	GTGATTCTATCTTTT[C/T]GCCTCCTGAGTAGTT	51147
rs577542172	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655643	TGGTTCTCACCATTC[C/G]GCAGGCAGTTCTCAG	51147
rs577565435	snp	A/G	0.000798403	0.0199641	intron-variant	ING4	GRCh38.p7	12:6654874	GGACTACAGGTGTGC[A/G]CCACCACATCTGGCT	51147
rs577958417	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ING4	GRCh38.p7	12:6664832	CGGTAACTTGATCTC[C/T]GTGCCTGTTTTACTA	51147
rs578117142	snp	A/C	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6657440	GGCGACACAGTGAGA[A/C]TCCATCTCAAACAAA	51147
rs578161178	snp	C/T	0.000399281	0.0141238	intron-variant	ING4	GRCh38.p7	12:6658386	AGCCAGAATGTCCTT[C/T]TTAAAAAATGCAAAC	51147
rs745386172	snp	A/C	1.6519e-05	0.00287388	intron-variant	ING4	GRCh38.p7	12:6651407	GAGGAAGAAAGAAGT[A/C]GTCAGGGGCCAGGAA	51147
rs745507238	snp	G/T	1.64789e-05	0.0028704	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652993	CAATCTGTTTCTCCT[G/T]GAGATCAGCCTCAAA	51147
rs745664771	snp	A/G	1.65449e-05	0.00287614	intron-variant	ING4	GRCh38.p7	12:6653220	TGGGGAGCCATGAAC[A/G]GGGCCATACCATCTC	51147
rs745701638	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6658763	CCGCTTATAACCTTC[C/T]GGTCACTTCCTACTG	51147
rs745907388	snp	C/G	1.65299e-05	0.00287483	missense, intron-variant	ING4	GRCh38.p7	12:6652413	GGCATCCCATACTCA[C/G]GACTTCTGCATGCCA	51147
rs746077743	snp	C/T	8.26562e-05	0.00642816	intron-variant	ING4	GRCh38.p7	12:6652635	GAAGAGGATGTCATC[C/T]GGCAAAGGGCTCCCT	51147
rs746272602	in-del	-/AT	3.31505e-05	0.00407113	intron-variant	ING4	GRCh38.p7	12:6663044	TGCAGCCCCGACCCC[-/AT]CACCTCCAGCCTGCT	51147
rs746401863	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6655351	ACCCGGCCCCAAATG[C/T]TTTAATATTGGAAGA	51147
rs746690936	snp	C/T	3.29679e-05	0.00405991	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653265	CAAGCTGCACCTTGT[C/T]GTCACCAAATTCCTT	51147
rs746944551	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6660567	GGGCCAAGATCGCAC[C/T]ATTGCGCTCCAGCCT	51147
rs747043769	snp	A/G	1.64754e-05	0.00287009	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652734	TTCCCTTTGGAACGA[A/G]CACGAGCAGCTTTCT	51147
rs747098954	snp	A/G	1.65149e-05	0.00287353	intron-variant	ING4	GRCh38.p7	12:6652642	ATGTCATCCGGCAAA[A/G]GGCTCCCTGAATCAC	51147
rs747291394	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6652029	TATGCTCAGCTAATT[C/T]TTGTATTTTTAGTAG	51147
rs747367807	snp	C/T	4.94703e-05	0.0049732	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6656773	CTGAAAGTTTCTCTG[C/T]AATTCAAAGGGAAGG	51147
rs747614878	snp	A/G	1.7033e-05	0.00291826	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6653380	AGTGGCCAACTTGTC[A/G]ATTTCAGCCTTCAGG	51147
rs747644839	snp	A/C	1.64762e-05	0.00287016	intron-variant	ING4	GRCh38.p7	12:6656706	CTCATTAGATACAAA[A/C]ACTTTTTACTCTATA	51147
rs747827789	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6655176	AGCCTCCTGAGTAGC[C/T]GGGATTACTGGCATG	51147
rs747947567	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6659057	CTTTCCCAGACTCTG[C/T]TAACTGCCCTCGATC	51147
rs748239980	snp	A/G	1.65037e-05	0.00287256	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6652958	GCCTTTGCTGGAAGA[A/G]CTGTCATAGTCACTT	51147
rs748329360	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6660880	GGAGTGCAATGGCGC[A/G]ATCTCAGGTTCAAGG	51147
rs748367799	snp	A/T	1.65373e-05	0.00287548	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6663062	CCTCCAGCCTGCTCT[A/T]ACTGTCCAGATAATG	51147
rs748497108	snp	A/G	1.65493e-05	0.00287652	intron-variant	ING4	GRCh38.p7	12:6651415	AAGAAGTAGTCAGGG[A/G]CCAGGAAGGGCCAGA	51147
rs748529172	snp	A/C/T	0.000199397	0.00998329	utr-variant-5-prime, upstream-variant-2KB	ING4	GRCh38.p7	12:6663133	GCAACTTCCGATCCG[A/C/T]CCCGGAAGTGACTGT	51147
rs748571571	snp	A/G	8.23784e-05	0.00641735	synonymous-codon, intron-variant	ING4	GRCh38.p7	12:6652337	GCAATAGGTGGGTTC[A/G]TTGGGATCCACAGGC	51147
rs748638891	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6654071	CGAACTCCTGGGTCA[A/T]GCAATCTGCCTGCTT	51147
rs748647234	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6651762	GGCCAGGCCAGTCTC[A/G]AACTCCTGATCTCAA	51147
rs748752846	snp	A/G	1.64789e-05	0.0028704	intron-variant	ING4	GRCh38.p7	12:6651256	CAGAGAAGGGGAGAG[A/G]AAAGTGAGTGAAAGG	51147
rs748783074	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6658561	GCTTGGTGCACATGC[C/T]TGTAATCCCAGCTAC	51147
rs748962515	in-del	-/CAAA			intron-variant	ING4	GRCh38.p7	12:6657452	AGACTCCATCTCAAA[-/CAAA]CAAACAAACAAACAA	51147
rs748984479	snp	C/T	1.64846e-05	0.0028709	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6652973	GCTGTCATAGTCACT[C/T]GACTCAATCTGTTTC	51147
rs749108024	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6655217	CCCGACTAATTTTTG[A/T]ATTTTTAGCAGAGAC	51147
rs749111377	snp	A/G	1.6513e-05	0.00287336	intron-variant	ING4	GRCh38.p7	12:6652808	GAAGGCAGGGAGACA[A/G]AAAGATGGGTTAAGT	51147
rs749515420	snp	A/G	3.33979e-05	0.0040863	intron-variant	ING4	GRCh38.p7	12:6651434	GGAAGGGCCAGAGGA[A/G]GGAGAGAAAGCCCCT	51147
rs749540146	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6662772	AAAAAATCTACCGAG[C/G]CTGGAGACCCTGGAG	51147
rs749568737	snp	A/G	1.66322e-05	0.00288371	utr-variant-5-prime, upstream-variant-2KB	ING4	GRCh38.p7	12:6663140	CCGATCCGCCCCGGA[A/G]GTGACTGTAACGCGA	51147
rs749696771	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6652177	TCTTTCTTCTATTCT[A/G]AAGTCCCAGTACTCA	51147
rs749832281	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6653201	GGATTAGATGGGAAG[C/T]AGGTGGGGAGCCATG	51147
rs749911348	snp	C/T	1.65422e-05	0.0028759	missense, intron-variant, nc-transcript-variant	ING4	GRCh38.p7	12:6652284	ACATCAGGGTTGTCA[C/T]AGCCAATCATCTCTC	51147
rs750314688	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6651914	TTAGAGTGTGGTGGC[A/G]TGATCTCAGCTCACT	51147
rs750616168	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6651682	AAGCAGCTGAGATTA[C/T]AGGCACAGGCTATCA	51147
rs750715990	snp	C/T	1.65518e-05	0.00287674	intron-variant	ING4	GRCh38.p7	12:6652919	CCCCACCTCTCACAG[C/T]CCCGCCCCCTCCTCA	51147
rs750817444	snp	A/G	3.29473e-05	0.00405864	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652713	GGGGCTTCTTCATCC[A/G]AGTTTTTCCCTTTGG	51147
rs750869703	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6657465	AACAAACAAACAAAC[A/G]AACAAAAAATAAAGT	51147
rs750965863	snp	C/G	4.94287e-05	0.00497111	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652679	GCGCACGAGCTTTAA[C/G]TTCTTCTGGGCAGTC	51147
rs751161754	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6663547	GAAGATCCAACTTTT[C/T]TTCCCTCTTTTGCAG	51147
rs751327177	snp	A/G	3.33039e-05	0.00408055	intron-variant	ING4	GRCh38.p7	12:6656824	GAGAGAAACAATCAC[A/G]GGACTGACTATGCAT	51147
rs751407963	in-del	-/C	1.65228e-05	0.00287422	intron-variant	ING4	GRCh38.p7	12:6651410	GAAGAAAGAAGTAGT[-/C]AGGGGCCAGGAAGGG	51147
rs751506832	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6654233	TGATTCTATCTTTTC[A/G]CCTCCTGAGTAGTTG	51147
rs751519940	snp	C/T	1.64803e-05	0.00287052	missense, utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651223	CGTTCTTGGGAGCAG[C/T]GTGGGCAAAACCTGA	51147
rs751750008	snp	C/G	1.65375e-05	0.0028755	intron-variant	ING4	GRCh38.p7	12:6652928	TCACAGCCCCGCCCC[C/G]TCCTCACTCTTTTTG	51147
rs751977103	snp	A/G	1.65968e-05	0.00288065	intron-variant	ING4	GRCh38.p7	12:6653095	TACAAAACTATCTCC[A/G]ATTAAAGAAAATAGG	51147
rs752009248	snp	C/G	1.65798e-05	0.00287917	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663119	CGAAGCAAAACAAAG[C/G]AACTTCCGATCCGCC	51147
rs752102738	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6657614	TATCCCACCCTTTTC[A/G]CCTTCAGTGACCTTC	51147
rs752176360	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6658159	GACACAGGGTTTCAC[C/T]ATTTTGGCCAGACTG	51147
rs752283198	snp	C/T			downstream-variant-500B	ING4	GRCh38.p7	12:6650295	TATAGTATAGCAGTA[C/T]GTATGTATAGCACAA	51147
rs752312402	snp	A/C	1.67027e-05	0.00288982	intron-variant	ING4	GRCh38.p7	12:6663018	CTCTCATCCCTGATC[A/C]CCGCACCACTCTGCA	51147
rs752467393	snp	A/G	1.64746e-05	0.00287002	synonymous-codon, missense, nc-transcript-variant	ING4	GRCh38.p7	12:6651365	CCCCACACAGGCAAA[A/G]TGGAACCACTCAATG	51147
rs752489636	snp	C/G	3.29571e-05	0.00405924	intron-variant	ING4	GRCh38.p7	12:6651248	ACCTGAAACAGAGAA[C/G]GGGAGAGAAAAGTGA	51147
rs752541785	snp	A/T	1.65482e-05	0.00287643	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663101	ACATCCCCGCAGCCA[A/T]CTCGAAGCAAAACAA	51147
rs752599785	in-del	-/C	1.65256e-05	0.00287447	intron-variant	ING4	GRCh38.p7	12:6652634	AGAAGAGGATGTCAT[-/C]CGGCAAAGGGCTCCC	51147
rs752733618	snp	A/G	1.65971e-05	0.00288067	intron-variant	ING4	GRCh38.p7	12:6653187	GTCTAAGACCCTGAG[A/G]ATTAGATGGGAAGTA	51147
rs752901157	snp	A/G			synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6652997	CTGTTTCTCCTTGAG[A/G]TCAGCCTCAAAACGG	51147
rs752937715	snp	A/G	1.6492e-05	0.00287154	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653321	TGTTTGAGAAGGGCC[A/G]ATTTTTCCTCGGAGC	51147
rs753288705	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6661912	ATCAACAATATCATG[A/C]TCCAATTTACCATAT	51147
rs753299645	snp	A/T	3.31362e-05	0.00407026	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663115	ATCTCGAAGCAAAAC[A/T]AAGCAACTTCCGATC	51147
rs753436197	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6660043	TTCTCTCCTGTTTCC[A/G]TAGTGTTTAGAATTA	51147
rs753462241	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6658360	ACACTTCCAATCTAC[C/T]TCCATATAGTAGCCA	51147
rs753775588	snp	G/T	4.9831e-05	0.00499129	intron-variant	ING4	GRCh38.p7	12:6653205	TAGATGGGAAGTAGG[G/T]GGGGAGCCATGAACA	51147
rs753830804	snp	A/G			downstream-variant-500B	ING4	GRCh38.p7	12:6650501	TAATTCTGGCATGCC[A/G]TCCTCTCACATTGCA	51147
rs753946853	in-del	-/CT	4.03979e-05	0.00449414	intron-variant	ING4	GRCh38.p7	12:6653432	TGGTCACAATGGCCC[-/CT]GAGTGGCTAGGTGAA	51147
rs754078294	snp	C/T			intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655739	CACAGCTTCATGTAT[C/T]TCAAAACCAGTCTGT	51147
rs754203499	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6654542	TGAGGTCTCACTATA[C/T]TGCCCAGGCTGGTCT	51147
rs754450163	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6661940	TATATTAGTCATTTT[A/C]CTCTATAAAAATCAT	51147
rs754590745	snp	C/T	1.64762e-05	0.00287016	intron-variant	ING4	GRCh38.p7	12:6656695	GATTACACACACTCA[C/T]TAGATACAAAAACTT	51147
rs754751153	snp	C/T	1.68363e-05	0.00290136	intron-variant	ING4	GRCh38.p7	12:6656848	TATGCATAGGCCTTA[C/T]AGCTCCTTTTAAAGT	51147
rs754910604	snp	A/G	3.29587e-05	0.00405934	intron-variant	ING4	GRCh38.p7	12:6651239	GTGGGCAAAACCTGA[A/G]ACAGAGAAGGGGAGA	51147
rs755046894	in-del	-/AA			intron-variant	ING4	GRCh38.p7	12:6657929	CGAGACTCTGTCTCC[-/AA]AAAAAAAAAAAAAAA	51147
rs755146214	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6652061	GAAGGGGTTACACTA[C/T]GTTGGCCAGGCTGGT	51147
rs755260705	snp	C/G	1.65149e-05	0.00287353	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6652952	CTTTTTGCCTTTGCT[C/G]GAAGAGCTGTCATAG	51147
rs755567519	snp	A/G	1.65814e-05	0.00287931	utr-variant-5-prime, upstream-variant-2KB	ING4	GRCh38.p7	12:6663120	GAAGCAAAACAAAGC[A/G]ACTTCCGATCCGCCC	51147
rs755599170	snp	C/T	1.6476e-05	0.00287014	intron-variant	ING4	GRCh38.p7	12:6656716	ACAAAAACTTTTTAC[C/T]CTATACATACCCTCT	51147
rs755649007	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6656696	ATTACACACACTCAT[G/T]AGATACAAAAACTTT	51147
rs755730835	snp	A/G	1.64792e-05	0.00287042	intron-variant	ING4	GRCh38.p7	12:6651250	CTGAAACAGAGAAGG[A/G]GAGAGAAAAGTGAGT	51147
rs755826465	snp	G/T	3.32646e-05	0.00407814	intron-variant	ING4	GRCh38.p7	12:6663028	TGATCCCCGCACCAC[G/T]CTGCAGCCCCGACCC	51147
rs755936146	snp	C/T	1.65021e-05	0.00287241	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652960	CTTTGCTGGAAGAGC[C/T]GTCATAGTCACTTGA	51147
rs756021538	in-del	-/AAGG	0.00016488	0.00907816	intron-variant	ING4	GRCh38.p7	12:6653060	GTCCACCTGGGTGGA[-/AAGG]AAGGAGAAAGGAGAG	51147
rs756045905	in-del	-/C			intron-variant	ING4	GRCh38.p7	12:6655972	TTTTTTTTCTTTCCT[-/C]TTTCTTTTTTCTTTC	51147
rs756236748	snp	C/G	4.97781e-05	0.00498864	intron-variant	ING4	GRCh38.p7	12:6653192	AGACCCTGAGGATTA[C/G]ATGGGAAGTAGGTGG	51147
rs756262814	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6662708	GGAGAGGTCTTTACC[A/G]CTTCTCCAAATGGCA	51147
rs756346204	snp	A/C			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651004	ACATACCGTTAGTGG[A/C]TGCGGCACCCCTCCC	51147
rs756480771	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6653104	ATCTCCAATTAAAGA[A/C]AATAGGTTAAGGCAG	51147
rs756630558	snp	C/G	1.67587e-05	0.00289466	intron-variant	ING4	GRCh38.p7	12:6652470	GAAGGGAAGCTAAAG[C/G]CTGAGGCTTTCAGAG	51147
rs756702696	snp	A/G/T	3.31429e-05	0.0040707	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663116	TCTCGAAGCAAAACA[A/G/T]AGCAACTTCCGATCC	51147
rs756751323	snp	C/T	1.64757e-05	0.00287012	missense, intron-variant	ING4	GRCh38.p7	12:6652338	CAATAGGTGGGTTCG[C/T]TGGGATCCACAGGCA	51147
rs756848334	snp	C/G	1.65913e-05	0.00288017	missense, intron-variant, nc-transcript-variant	ING4	GRCh38.p7	12:6652276	TGTTTCTCACATCAG[C/G]GTTGTCACAGCCAAT	51147
rs756881685	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6658688	AAGACACTGACTCAA[A/G]AAAACAAAAACAAAA	51147
rs757205535	snp	A/G	1.65718e-05	0.00287848	intron-variant	ING4	GRCh38.p7	12:6653208	ATGGGAAGTAGGTGG[A/G]GAGCCATGAACAGGG	51147
rs757214932	snp	C/T			downstream-variant-500B	ING4	GRCh38.p7	12:6650174	GAGAATCACTTGAAC[C/T]CGGAGGCGGAGACTG	51147
rs757277262	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6663932	TCACCGCAACCTCCA[C/T]CTCCCGGGTTCAAGT	51147
rs757423580	in-del	-/C			upstream-variant-2KB	ING4	GRCh38.p7	12:6663538	CAGCAACTGGAAGAT[-/C]CAACTTTTTTTCCCT	51147
rs757476508	in-del	-/T	0.000373378	0.0136583	intron-variant	ING4	GRCh38.p7	12:6655956	ATTGTCAATTACTGC[-/T]TTTTTTTTCTTTCCT	51147
rs757576765	snp	A/G			intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6655776	CTTGAACATGGCTAC[A/G]TAGAATGAAGACAAG	51147
rs757610051	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6654688	CATTTTCCATTACTT[A/C]TTTTTTTCCTGTTTG	51147
rs757715279	snp	G/T	1.65384e-05	0.00287557	intron-variant	ING4	GRCh38.p7	12:6652618	AGTGGGGCACCGGGA[G/T]AGAAGAGGATGTCAT	51147
rs757726352	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6661821	CTTTCATATTTAACT[C/T]CTAAATACTTCTGTA	51147
rs757805619	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6658219	CCCGCCTTGATCTCC[C/T]AAAGTGCTGGGATTA	51147
rs757869141	snp	G/T	1.64857e-05	0.00287099	missense, intron-variant, nc-transcript-variant	ING4	GRCh38.p7	12:6652305	ATCATCTCTCCATAG[G/T]AGACCTGGTGACAAA	51147
rs757875100	snp	C/T	3.29473e-05	0.00405864	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652695	TTCTTCTGGGCAGTC[C/T]TGGGGGCTTCTTCAT	51147
rs758248975	snp	A/C/G	3.31358e-05	0.00407026	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6653347	GGAGCTCAGGCTGCG[A/C/G]GCACTACTCATATAC	51147
rs758405383	snp	A/C			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650745	TGACCTGGTGGATCC[A/C]CCACCATGAAAAAAG	51147
rs758476446	snp	C/T	4.94295e-05	0.00497115	intron-variant	ING4	GRCh38.p7	12:6656687	AAATAAATGATTACA[C/T]ACACTCATTAGATAC	51147
rs758814963	snp	C/T	1.65515e-05	0.00287671	intron-variant	ING4	GRCh38.p7	12:6652922	CACCTCTCACAGCCC[C/T]GCCCCCTCCTCACTC	51147
rs759144922	snp	C/T	1.64757e-05	0.00287012	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652684	CGAGCTTTAACTTCT[C/T]CTGGGCAGTCTTGGG	51147
rs759149903	snp	A/G	0.0001821	0.00954026	intron-variant	ING4	GRCh38.p7	12:6651420	GTAGTCAGGGGCCAG[A/G]AAGGGCCAGAGGAAG	51147
rs759298293	in-del	-/A	0.00011571	0.00760537	intron-variant	ING4	GRCh38.p7	12:6651411	AAGAAAGAAGTAGTC[-/A]GGGGCCAGGAAGGGC	51147
rs759307134	snp	G/T	1.65433e-05	0.002876	intron-variant	ING4	GRCh38.p7	12:6652819	GACAGAAAGATGGGT[G/T]AAGTCCTCTTCTCTC	51147
rs759537062	snp	A/C	1.70284e-05	0.00291786	intron-variant	ING4	GRCh38.p7	12:6652233	CACTCCCTTCATGCC[A/C]CTCACAACCCCCCAT	51147
rs759666403	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6654252	CCTGAGTAGTTGAGT[A/G]TATCACACAATTTAA	51147
rs759885140	in-del	-/CAAACAAA			intron-variant	ING4	GRCh38.p7	12:6657448	AGTGAGACTCCATCT[-/CAAACAAA]CAAACAAACAAACAA	51147
rs759924168	snp	A/G	1.64855e-05	0.00287097	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6653314	CTGGATCTGTTTGAG[A/G]AGGGCCAATTTTTCC	51147
rs760081406	snp	A/G	1.87958e-05	0.00306554	intron-variant	ING4	GRCh38.p7	12:6653412	CTACAACAGAGACAG[A/G]GGCCTGGTCACAATG	51147
rs760247479	in-del	-/G			intron-variant	ING4	GRCh38.p7	12:6653163	GATCCCAACACAGTT[-/G]AAGGAGGGGTCTAAG	51147
rs760261069	snp	A/T	1.65515e-05	0.00287671	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663103	ATCCCCGCAGCCATC[A/T]CGAAGCAAAACAAAG	51147
rs760267807	snp	C/T	1.648e-05	0.0028705	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653040	TCCAGCCGCCGAATG[C/T]GTTTGTCCACCTGGG	51147
rs760396496	snp	A/G			synonymous-codon, intron-variant	ING4	GRCh38.p7	12:6652331	ACAAAGGCAATAGGT[A/G]GGTTCGTTGGGATCC	51147
rs760710150	snp	C/G	1.69559e-05	0.00291164	intron-variant	ING4	GRCh38.p7	12:6652243	ATGCCCCTCACAACC[C/G]CCCATCCTAAGGCAA	51147
rs760842387	snp	C/T	1.64972e-05	0.00287199	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653325	TGAGAAGGGCCAATT[C/T]TTCCTCGGAGCTCAG	51147
rs760935262	snp	C/T	4.00689e-05	0.00447581	intron-variant	ING4	GRCh38.p7	12:6653429	GCCTGGTCACAATGG[C/T]CCCTGAGTGGCTAGG	51147
rs761224013	snp	C/G	1.65416e-05	0.00287586	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651157	TAGCCCAAGTCAGGG[C/G]ATGTGGAAGAAACTG	51147
rs761491214	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6653848	TGTACATCAATATCA[C/T]ACATTTCAAAATTAT	51147
rs761563151	in-del	-/CAAGTGATCTGCTCACCTTGGCCTCCCAAAGTGCTGGGA			intron-variant	ING4	GRCh38.p7	12:6651775	TCGAACTCCTGATCT[lengthTooLong]TTACAGGCGTGAGCC	51147
rs761628715	snp	C/T	4.99513e-05	0.00499731	intron-variant	ING4	GRCh38.p7	12:6652450	AGAGAAAGTGTCATC[C/T]ACAGGAAGGGAAGCT	51147
rs761760819	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6652488	GAGGCTTTCAGAGGT[A/G]GCAGGAGATCCTGGT	51147
rs761779127	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6659013	TATTAAATTCCTGTT[C/T]GTTCTTCCAAAGTTC	51147
rs761787934	snp	A/G	1.65113e-05	0.00287322	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6653332	GGCCAATTTTTCCTC[A/G]GAGCTCAGGCTGCGG	51147
rs761788243	snp	A/C	1.64887e-05	0.00287125	splice-donor-variant	ING4	GRCh38.p7	12:6652661	TCCCTGAATCACTCA[A/C]GTGCGCACGAGCTTT	51147
rs762010414	snp	C/T	0.000185684	0.00963366	intron-variant, splice-acceptor-variant	ING4	GRCh38.p7	12:6655915	GGTATCTAATGCTTC[C/T]GTAAGTGTGAACGGT	51147
rs762083143	snp	A/C	1.65266e-05	0.00287455	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651168	AGGGGATGTGGAAGA[A/C]ACTGTGTTGGAATCC	51147
rs762113084	snp	A/G	0.000313229	0.0125107	intron-variant	ING4	GRCh38.p7	12:6651388	ACTCAATGGAACACT[A/G]GAAGAGGAAGAAAGA	51147
rs762169945	snp	C/T	1.65548e-05	0.002877	splice-acceptor-variant, intron-variant	ING4	GRCh38.p7	12:6656800	AAGGTTTTCAATACC[C/T]AGGGAAGAGAGAGAA	51147
rs762356027	snp	C/T	4.96718e-05	0.00498331	intron-variant	ING4	GRCh38.p7	12:6652910	CAGTCCTCGCCCCAC[C/T]TCTCACAGCCCCGCC	51147
rs762583768	in-del	-/A	1.64784e-05	0.00287035	intron-variant	ING4	GRCh38.p7	12:6651256	CAGAGAAGGGGAGAG[-/A]AAAGTGAGTGAAAGG	51147
rs762652667	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6652429	GACTTCTGCATGCCA[A/G]GAGGAAGAGAAAGTG	51147
rs762705934	snp	A/G	1.66835e-05	0.00288816	intron-variant	ING4	GRCh38.p7	12:6652459	GTCATCTACAGGAAG[A/G]GAAGCTAAAGCCTGA	51147
rs762763512	snp	A/G	3.30989e-05	0.00406797	intron-variant	ING4	GRCh38.p7	12:6652614	TGGGAGTGGGGCACC[A/G]GGAGAGAAGAGGATG	51147
rs762791573	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6654033	GTAGAGACAGGCTTT[C/T]TCCACGTTACCCAGG	51147
rs763197542	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6661049	TCCACCCATCTCAGC[C/G]TCCCAATGTGCTAGG	51147
rs763315307	snp	A/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6663729	CTACTTATAAATACA[A/G]AGAATGACTCATAAT	51147
rs763315561	snp	C/T	0.000197668	0.00993955	missense, utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651327	CCTGCCACTTACCAT[C/T]TCCCCCGAGGCTTGG	51147
rs763381041	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6657466	ACAAACAAACAAACA[A/C]ACAAAAAATAAAGTG	51147
rs763504655	snp	C/T	4.94425e-05	0.0049718	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653300	TTGCCATAGGCTTCC[C/T]GGATCTGTTTGAGAA	51147
rs763738041	snp	A/G	1.65652e-05	0.0028779	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663110	CAGCCATCTCGAAGC[A/G]AAACAAAGCAACTTC	51147
rs763876954	snp	A/G	1.67435e-05	0.00289335	intron-variant	ING4	GRCh38.p7	12:6652262	ATCCTAAGGCAAAAT[A/G]TTTCTCACATCAGGG	51147
rs764177048	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6657342	TACTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	51147
rs764227924	snp	C/T	1.65094e-05	0.00287305	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653331	GGGCCAATTTTTCCT[C/T]GGAGCTCAGGCTGCG	51147
rs764230556	snp	C/T	4.03364e-05	0.00449072	intron-variant	ING4	GRCh38.p7	12:6653430	CCTGGTCACAATGGC[C/T]CCTGAGTGGCTAGGT	51147
rs764362480	snp	A/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6663733	TTATAAATACAAAGA[A/G]TGACTCATAATAAAG	51147
rs764591616	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6661121	TTTTTTTTTTGAGGC[A/G]GAGTCTCACTCTGTT	51147
rs764644678	snp	C/G/T	8.23722e-05	0.00641717	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652690	TTAACTTCTTCTGGG[C/G/T]AGTCTTGGGGGCTTC	51147
rs764668745	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6662316	ATGTATTTCCATTAT[C/T]TCACTTGTCACAGTG	51147
rs765067593	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6652612	GCTGGGAGTGGGGCA[C/T]CGGGAGAGAAGAGGA	51147
rs765335247	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6651913	GTTAGAGTGTGGTGG[C/T]GTGATCTCAGCTCAC	51147
rs765393538	snp	C/T	1.64939e-05	0.0028717	missense, utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651200	AGGCCCTTATCTATT[C/T]CTTCTTCCGTTCTTG	51147
rs765459341	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6657665	CGTCAGGTGTGGTGG[C/T]TCAAGCCTGTAATCC	51147
rs765572311	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6656087	TAACATTAACAATGA[C/G]AGAAGTAGAAACATT	51147
rs765616119	snp	A/T	3.30158e-05	0.00406286	intron-variant	ING4	GRCh38.p7	12:6653070	GTGGAAAGGAAGGAG[A/T]AAGGAGAGGTACAAA	51147
rs765642984	in-del	-/T			intron-variant	ING4	GRCh38.p7	12:6659690	GGTGGCGGGCGCCTG[-/T]TAGTCCCAGCTACTC	51147
rs765907419	snp	A/G			downstream-variant-500B	ING4	GRCh38.p7	12:6650070	CATCCTGGCCAACAC[A/G]GTGAAACCCTGTCTC	51147
rs765926378	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6662343	AGTGTTTTATAATTA[C/T]TTGCAGAATCTGTTT	51147
rs766007221	in-del	-/AGTG	1.6478e-05	0.00287032	intron-variant	ING4	GRCh38.p7	12:6651259	AGAAGGGGAGAGAAA[-/AGTG]AGTGAAAGGGAGAAT	51147
rs766066455	snp	C/G	1.64776e-05	0.00287028	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652672	CTCACGTGCGCACGA[C/G]CTTTAACTTCTTCTG	51147
rs766125353	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6663507	TTTAGGCTCATATTG[C/T]GTAAACATACCTTCT	51147
rs766370563	snp	A/G	1.64822e-05	0.00287068	stop-gained, utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651215	TCTTCTTCCGTTCTT[A/G]GGAGCAGCGTGGGCA	51147
rs766376818	in-del	-/TT			intron-variant	ING4	GRCh38.p7	12:6656171	TTTCTTTAATTCTTC[-/TT]TTTTTTTTTTTTTTT	51147
rs766535244	snp	A/G	1.64741e-05	0.00286998	missense, utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651337	ACCATTTCCCCCGAG[A/G]CTTGGTTGTCAGCCC	51147
rs766599047	snp	A/T			intron-variant	ING4	GRCh38.p7	12:6654061	AGGCTGGTCTCGAAC[A/T]CCTGGGTCAAGCAAT	51147
rs766704155	snp	A/G	1.65504e-05	0.00287662	intron-variant	ING4	GRCh38.p7	12:6652923	ACCTCTCACAGCCCC[A/G]CCCCCTCCTCACTCT	51147
rs766727834	snp	A/C	1.656e-05	0.00287745	intron-variant	ING4	GRCh38.p7	12:6653089	GAGAGGTACAAAACT[A/C]TCTCCAATTAAAGAA	51147
rs767100666	snp	A/G	1.6641e-05	0.00288448	intron-variant	ING4	GRCh38.p7	12:6652897	TTCTTCTCCCTTTCA[A/G]TCCTCGCCCCACCTC	51147
rs767154677	snp	A/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6663705	AACTTGAGAAAGATG[A/T]TCACCTTTCTACTTA	51147
rs767207980	snp	A/C	1.65405e-05	0.00287576	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663096	CAAATACATCCCCGC[A/C]GCCATCTCGAAGCAA	51147
rs767237719	snp	C/T			downstream-variant-500B	ING4	GRCh38.p7	12:6650206	AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG	51147
rs767261395	in-del	-/GGGCCAGGAA	1.65323e-05	0.00287505	intron-variant	ING4	GRCh38.p7	12:6651413	GAAAGAAGTAGTCAG[-/GGGCCAGGAA]GGGCCAGAGGAAGGA	51147
rs767367162	snp	A/C	1.64741e-05	0.00286998	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6651356	GGTTGTCAGCCCCAC[A/C]CAGGCAAAATGGAAC	51147
rs767390198	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6653631	TAGTTGGAATTTAAA[C/T]TACTGAAACACAGCA	51147
rs767393351	snp	A/G	1.67854e-05	0.00289697	intron-variant	ING4	GRCh38.p7	12:6663014	GATCCTCTCATCCCT[A/G]ATCCCCGCACCACTC	51147
rs767525099	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6654292	TTACTCCAACATCCA[C/T]GTAACAATTCTGCTT	51147
rs767612788	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6655471	CTCTAACATAGTGCA[C/G]CAACAGATAACCAGG	51147
rs767623274	snp	C/G			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650679	TCTCCCAGGATGAAT[C/G]CTCTTGGCACAGAGG	51147
rs767676441	snp	C/T	1.64909e-05	0.00287144	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653319	TCTGTTTGAGAAGGG[C/T]CAATTTTTCCTCGGA	51147
rs767836885	in-del	-/ATT			upstream-variant-2KB	ING4	GRCh38.p7	12:6664643	GGATGTATTTGAAAC[-/ATT]ATCTGGACAGTAAGA	51147
rs768108985	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6662035	CTCTTTCTCCAGTCT[C/T]CTTTCTCAATTTCTT	51147
rs768182564	snp	A/G	3.29663e-05	0.00405981	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6653266	AAGCTGCACCTTGTC[A/G]TCACCAAATTCCTTG	51147
rs768252858	snp	C/T	1.67405e-05	0.00289309	missense, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6653367	TACTCATATACTCAG[C/T]GGCCAACTTGTCAAT	51147
rs768319555	in-del	-/CGAGACTCTGTCT			intron-variant	ING4	GRCh38.p7	12:6657915	AGCCTGGTGACAGAG[-/CGAGACTCTGTCT]CCAAAAAAAAAAAAA	51147
rs768542011	snp	C/T	1.65037e-05	0.00287256	intron-variant	ING4	GRCh38.p7	12:6652649	CCGGCAAAGGGCTCC[C/T]TGAATCACTCACGTG	51147
rs768597105	snp	A/G	3.32353e-05	0.00407634	intron-variant	ING4	GRCh38.p7	12:6652442	CAAGAGGAAGAGAAA[A/G]TGTCATCTACAGGAA	51147
rs768627580	in-del	-/CT			downstream-variant-500B	ING4	GRCh38.p7	12:6650415	CCTACCCTCCAGCAC[-/CT]CTGTCTTTCCCAAGT	51147
rs768689646	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6660727	CAAGACTGAGTCACT[A/G]GTGATTTACCAAATC	51147
rs768874368	snp	C/T	1.65422e-05	0.0028759	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6663059	CCACCTCCAGCCTGC[C/T]CTTACTGTCCAGATA	51147
rs768877523	snp	A/G/T	4.95957e-05	0.00497954	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6656794	AAAGGGAAGGTTTTC[A/G/T]ATACCTAGGGAAGAG	51147
rs769016322	snp	G/T			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650835	AATGAAGAGGTCTGG[G/T]GGACTGCCCCCATGC	51147
rs769037284	snp	A/G	4.95954e-05	0.00497948	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651164	AGTCAGGGGATGTGG[A/G]AGAAACTGTGTTGGA	51147
rs769103240	snp	C/G	6.59e-05	0.00573983	intron-variant	ING4	GRCh38.p7	12:6651286	GGAGAATGCCCTTGA[C/G]CACTCAACTTAGGGA	51147
rs769576351	snp	A/T			missense, intron-variant, nc-transcript-variant	ING4	GRCh38.p7	12:6652278	TTTCTCACATCAGGG[A/T]TGTCACAGCCAATCA	51147
rs769827276	snp	C/G	1.6492e-05	0.00287154	intron-variant	ING4	GRCh38.p7	12:6652783	CTTCTAGGGAAGAGG[C/G]AGAAAGCCAGAAGGC	51147
rs769985900	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6660917	TGTGCCTCAGCCTCC[A/C]AAGTAGCTGGGATTA	51147
rs770019196	snp	C/T	4.94205e-05	0.0049707	intron-variant	ING4	GRCh38.p7	12:6651316	ACCCTCCAACTCCTG[C/T]CACTTACCATTTCCC	51147
rs770292806	snp	C/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6664678	AGGCTGGAGGAGGGG[C/G]TTCAGGGGCTGTAGA	51147
rs770337349	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651175	GTGGAAGAAACTGTG[C/T]TGGAATCCAAGGCCC	51147
rs770410492	snp	G/T	1.64773e-05	0.00287026	intron-variant	ING4	GRCh38.p7	12:6651264	GGGAGAGAAAAGTGA[G/T]TGAAAGGGAGAATGC	51147
rs770447830	snp	A/G	3.30415e-05	0.00406444	intron-variant	ING4	GRCh38.p7	12:6652811	GGCAGGGAGACAGAA[A/G]GATGGGTTAAGTCCT	51147
rs770734842	snp	C/T	1.64795e-05	0.00287045	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652986	CTTGACTCAATCTGT[C/T]TCTCCTTGAGATCAG	51147
rs771207486	snp	C/G	1.64993e-05	0.00287218	missense, intron-variant	ING4	GRCh38.p7	12:6652400	AAAGGTCACTGAGGG[C/G]ATCCCATACTCAGGA	51147
rs771235643	in-del	-/CTCT			upstream-variant-2KB	ING4	GRCh38.p7	12:6664154	TGGCCCCTCTTGCTA[-/CTCT]CTAAGGGGGAAATCT	51147
rs771294127	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6653535	ATGTTCAGAGGTACT[C/G]TGCCATGCACTCAAG	51147
rs771336056	snp	A/G	3.34202e-05	0.00408766	intron-variant	ING4	GRCh38.p7	12:6651435	GAAGGGCCAGAGGAA[A/G]GAGAGAAAGCCCCTC	51147
rs771387644	snp	A/C/G	3.68754e-05	0.00429378	intron-variant	ING4	GRCh38.p7	12:6653407	CAGGTCTACAACAGA[A/C/G]ACAGAGGCCTGGTCA	51147
rs771439114	snp	C/T	4.94458e-05	0.00497197	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6653308	GGCTTCCTGGATCTG[C/T]TTGAGAAGGGCCAAT	51147
rs771450392	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6661055	CATCTCAGCCTCCCA[A/G]TGTGCTAGGATTATA	51147
rs771814489	snp	A/G	1.6543e-05	0.00287597	intron-variant	ING4	GRCh38.p7	12:6653221	GGGGAGCCATGAACA[A/G]GGCCATACCATCTCA	51147
rs771849721	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6658915	TGTGCTCCTCCTGCC[A/G]TTTGGCTTTCCACAT	51147
rs771867837	snp	G/T	1.6477e-05	0.00287024	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653018	CTCAAAACGGGCCAG[G/T]TCTGTGTCCAGCCGC	51147
rs772019749	snp	C/G	4.95929e-05	0.00497936	missense, intron-variant	ING4	GRCh38.p7	12:6652414	GCATCCCATACTCAG[C/G]ACTTCTGCATGCCAA	51147
rs772045702	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6657262	AGACCATCCTGGCTA[A/C]CATGGTGAAACCCCG	51147
rs772077815	in-del	-/TTC			intron-variant	ING4	GRCh38.p7	12:6651544	ACCATCTTCCTTCTA[-/TTC]TTTTTTTCTTTTTGA	51147
rs772489910	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6664264	CACTACTGGGCTAGT[C/T]GGCTAGTTAGTTGCT	51147
rs772498435	snp	C/T	4.96808e-05	0.00498377	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651146	CCTCTGCCCACTAGC[C/T]CAAGTCAGGGGATGT	51147
rs772593595	in-del	-/G	1.65564e-05	0.00287714	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663105	CCCCGCAGCCATCTC[-/G]AAGCAAAACAAAGCA	51147
rs772623309	snp	A/C	1.64833e-05	0.00287078	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6656763	CCCTCATGAGCTGAA[A/C]GTTTCTCTGTAATTC	51147
rs772838388	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6653994	CAGGCACCACCACGC[A/C]TGGCTAATTTTTTCT	51147
rs773073960	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6657020	TTAGCCTAGTGTGAC[A/G]GTGGGCATCTCTAAT	51147
rs773124829	snp	A/G	1.64827e-05	0.00287073	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652666	GAATCACTCACGTGC[A/G]CACGAGCTTTAACTT	51147
rs773376339	snp	A/G	0.000345496	0.0131388	intron-variant	ING4	GRCh38.p7	12:6653418	CAGAGACAGAGGCCT[A/G]GTCACAATGGCCCCT	51147
rs773585948	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6660982	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTATGTT	51147
rs773591998	snp	C/T	1.64738e-05	0.00286995	intron-variant	ING4	GRCh38.p7	12:6651321	CCAACTCCTGCCACT[C/T]ACCATTTCCCCCGAG	51147
rs773748349	snp	A/G	3.30579e-05	0.00406544	intron-variant	ING4	GRCh38.p7	12:6653079	AAGGAGAAAGGAGAG[A/G]TACAAAACTATCTCC	51147
rs774132579	snp	C/G	1.65353e-05	0.00287531	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663090	ATGTTCCAAATACAT[C/G]CCCGCAGCCATCTCG	51147
rs774164564	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6652802	AAGCCAGAAGGCAGG[C/G]AGACAGAAAGATGGG	51147
rs774166200	snp	G/T	1.65217e-05	0.00287412	intron-variant	ING4	GRCh38.p7	12:6652812	GCAGGGAGACAGAAA[G/T]ATGGGTTAAGTCCTC	51147
rs774323936	snp	A/C	4.94368e-05	0.00497152	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652988	TGACTCAATCTGTTT[A/C]TCCTTGAGATCAGCC	51147
rs774404033	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6662796	CCTGGAGAATGGGGG[C/T]AGCAACTATCTTCCT	51147
rs774512004	snp	A/G	1.7056e-05	0.00292022	intron-variant	ING4	GRCh38.p7	12:6652230	ACCCACTCCCTTCAT[A/G]CCCCTCACAACCCCC	51147
rs774629147	snp	C/T	1.64825e-05	0.00287071	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653309	GCTTCCTGGATCTGT[C/T]TGAGAAGGGCCAATT	51147
rs774887949	snp	A/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6663799	ACGTTACACTAGAAT[A/G]CACTTTCACATATAA	51147
rs775078189	snp	C/T	1.64773e-05	0.00287026	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6653027	GGCCAGGTCTGTGTC[C/T]AGCCGCCGAATGTGT	51147
rs775201017	snp	C/T	3.3211e-05	0.00407485	intron-variant	ING4	GRCh38.p7	12:6652902	CTCCCTTTCAGTCCT[C/T]GCCCCACCTCTCACA	51147
rs775375521	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6657276	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	51147
rs775689156	in-del	-/G			intron-variant	ING4	GRCh38.p7	12:6661413	AGCCTTTGTTTTTTT[-/G]TTTTTTTTTTTTTTT	51147
rs775709391	snp	A/C	1.65359e-05	0.00287536	missense, intron-variant	ING4	GRCh38.p7	12:6652415	CATCCCATACTCAGG[A/C]CTTCTGCATGCCAAG	51147
rs775783201	snp	A/G	7.83945e-05	0.00626028	intron-variant	ING4	GRCh38.p7	12:6653425	AGAGGCCTGGTCACA[A/G]TGGCCCCTGAGTGGC	51147
rs775864383	snp	A/G	1.64841e-05	0.00287085	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6656764	CCTCATGAGCTGAAA[A/G]TTTCTCTGTAATTCA	51147
rs775931428	snp	G/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6663154	AAGTGACTGTAACGC[G/T]ACAGGGGCCGAAGCC	51147
rs776004906	snp	A/G	1.65452e-05	0.00287616	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651155	ACTAGCCCAAGTCAG[A/G]GGATGTGGAAGAAAC	51147
rs776073675	snp	A/T	1.64795e-05	0.00287045	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653276	TTGTCGTCACCAAAT[A/T]CCTTGCACTTGCCAT	51147
rs776346199	snp	A/G	1.66261e-05	0.00288319	intron-variant	ING4	GRCh38.p7	12:6652444	AGAGGAAGAGAAAGT[A/G]TCATCTACAGGAAGG	51147
rs776420954	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6652477	AGCTAAAGCCTGAGG[A/C]TTTCAGAGGTGGCAG	51147
rs776437270	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6653819	AGTCATCTGCTGTTG[C/T]TGGTTTCCAAGTCTG	51147
rs776574713	snp	C/T	1.64914e-05	0.00287149	intron-variant	ING4	GRCh38.p7	12:6652658	GGCTCCCTGAATCAC[C/T]CACGTGCGCACGAGC	51147
rs776575745	snp	A/G			missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	ING4	GRCh38.p7	12:6663077	TACTGTCCAGATAAT[A/G]TTCCAAATACATCCC	51147
rs776610033	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6660477	AGCTGGGTATGGTGG[C/T]GGGCACTGTAATCCT	51147
rs776722652	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6657362	GCTGAGGCAGGAGAA[C/T]GGCATGAACCTGGGA	51147
rs776735730	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6653431	CTGGTCACAATGGCC[C/T]CTGAGTGGCTAGGTG	51147
rs776929757	snp	C/G	1.65299e-05	0.00287483	utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6651166	TCAGGGGATGTGGAA[C/G]AAACTGTGTTGGAAT	51147
rs776945203	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650957	AGTGGGCAAGACCAC[A/G]TCCCTCCGAAGGGAG	51147
rs776998174	snp	C/T	1.64749e-05	0.00287005	intron-variant	ING4	GRCh38.p7	12:6651304	CTCAACTTAGGGACC[C/T]TCCAACTCCTGCCAC	51147
rs777120852	snp	C/T	1.65397e-05	0.00287569	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6663061	ACCTCCAGCCTGCTC[C/T]TACTGTCCAGATAAT	51147
rs777121159	snp	G/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6664437	AGTAAGATAGTATTT[G/T]AGAGATAGCTGCCAC	51147
rs777249753	snp	A/G	3.32491e-05	0.00407719	intron-variant	ING4	GRCh38.p7	12:6663031	TCCCCGCACCACTCT[A/G]CAGCCCCGACCCCCA	51147
rs777301239	snp	A/G	1.64762e-05	0.00287016	stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6656739	TACCCTCTGTTCTTT[A/G]GTCTAGGTCCCTCAT	51147
rs777403717	snp	C/G	1.64787e-05	0.00287038	intron-variant	ING4	GRCh38.p7	12:6651251	TGAAACAGAGAAGGG[C/G]AGAGAAAAGTGAGTG	51147
rs777485323	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6652244	TGCCCCTCACAACCC[C/T]CCATCCTAAGGCAAA	51147
rs777570471	snp	A/C			intron-variant	ING4	GRCh38.p7	12:6662848	AAGACACGTCTCTAA[A/C]CCCCACACCGCACCC	51147
rs777719835	in-del	-/AAAG	1.66078e-05	0.00288161	intron-variant	ING4	GRCh38.p7	12:6653099	AAACTATCTCCAATT[-/AAAG]AAAATAGGTTAAGGC	51147
rs777760797	snp	A/G	1.65853e-05	0.00287964	intron-variant	ING4	GRCh38.p7	12:6653199	GAGGATTAGATGGGA[A/G]GTAGGTGGGGAGCCA	51147
rs777827472	snp	A/G			upstream-variant-2KB	ING4	GRCh38.p7	12:6663786	TCAGAGCTCCTGTAC[A/G]TTACACTAGAATACA	51147
rs777929309	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6653190	TAAGACCCTGAGGAT[G/T]AGATGGGAAGTAGGT	51147
rs778267798	snp	A/G	1.64784e-05	0.00287035	synonymous-codon, intron-variant	ING4	GRCh38.p7	12:6652373	CAACACATCAGAGGG[A/G]TGGACACTGCCAAAG	51147
rs778271835	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6658121	CGCGCCACCACACCC[A/G]ACTAATTTTTGTATT	51147
rs778357966	snp	C/G			intron-variant	ING4	GRCh38.p7	12:6654876	ACTACAGGTGTGCGC[C/G]ACCACATCTGGCTAA	51147
rs778368591	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6656602	TAAGAATTCCAAGAG[C/T]GTAAAAAAGGAGCGA	51147
rs778384841	snp	C/G	6.60589e-05	0.00574675	intron-variant	ING4	GRCh38.p7	12:6651405	AAGAGGAAGAAAGAA[C/G]TAGTCAGGGGCCAGG	51147
rs778438080	snp	A/C	1.64757e-05	0.00287012	intron-variant	ING4	GRCh38.p7	12:6651280	TGAAAGGGAGAATGC[A/C]CTTGACCACTCAACT	51147
rs778513676	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6658752	AAGTCACTCTCCCGC[C/T]TATAACCTTCTGGTC	51147
rs778971197	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650915	CTCTGAAATACAGCA[-/C]CGACCTCAGCATGGA	51147
rs779028072	snp	C/T	1.65534e-05	0.00287688	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6653342	TCCTCGGAGCTCAGG[C/T]TGCGGGCACTACTCA	51147
rs779154901	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6650600	GCAGGCCAACATGTA[C/T]AGCTTTTATTTACCT	51147
rs779251602	snp	C/T			upstream-variant-2KB	ING4	GRCh38.p7	12:6664001	AGGTATGCACCATCA[C/T]GCCAGACTAATTTTG	51147
rs779253099	in-del	-/CCC	3.31741e-05	0.00407259	intron-variant	ING4	GRCh38.p7	12:6663041	ACTCTGCAGCCCCGA[-/CCC]CCACCTCCAGCCTGC	51147
rs779346817	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6654732	TTGCTCCAAACACGT[C/T]TTTTTGTTTTGAGAC	51147
rs779380349	snp	G/T	1.6531e-05	0.00287493	intron-variant	ING4	GRCh38.p7	12:6652626	ACCGGGAGAGAAGAG[G/T]ATGTCATCCGGCAAA	51147
rs779446808	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6653499	ATTGATTAGCATAAC[C/T]TTCCAACTAAAAAGT	51147
rs779451017	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6653622	TTGCTATCATAGTTG[A/G]AATTTAAATTACTGA	51147
rs779478011	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6658478	ATCAGCTGAGCTGAG[A/G]AGTTCAAGACCAGCC	51147
rs779664155	snp	A/G	1.64795e-05	0.00287045	synonymous-codon, intron-variant	ING4	GRCh38.p7	12:6652316	ATAGGAGACCTGGTG[A/G]CAAAGGCAATAGGTG	51147
rs779878226	snp	C/T	9.8912e-05	0.0070318	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6653260	CATGGCAAGCTGCAC[C/T]TTGTCGTCACCAAAT	51147
rs780024484	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6658929	CATTTGGCTTTCCAC[A/G]TGCTGTTCTCTCTAG	51147
rs780449534	snp	C/G/T	3.30935e-05	0.00406766	intron-variant, utr-variant-5-prime	ING4	GRCh38.p7	12:6663056	CCCCCACCTCCAGCC[C/G/T]GCTCTTACTGTCCAG	51147
rs780687768	snp	C/T			intron-variant	ING4	GRCh38.p7	12:6656421	CTCAAGTTACCTGCC[C/T]GCCTAGGCCTCCCAA	51147
rs780697041	snp	A/G	3.34801e-05	0.00409132	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ING4	GRCh38.p7	12:6653368	ACTCATATACTCAGT[A/G]GCCAACTTGTCAATT	51147
rs780737527	snp	A/G	1.64765e-05	0.00287019	intron-variant	ING4	GRCh38.p7	12:6656698	TACACACACTCATTA[A/G]ATACAAAAACTTTTT	51147
rs781034481	snp	A/T	4.94344e-05	0.00497139	intron-variant	ING4	GRCh38.p7	12:6651246	AAACCTGAAACAGAG[A/T]AGGGGAGAGAAAAGT	51147
rs781235583	snp	A/C	1.65094e-05	0.00287305	synonymous-codon, nc-transcript-variant	ING4	GRCh38.p7	12:6652955	TTTGCCTTTGCTGGA[A/C]GAGCTGTCATAGTCA	51147
rs781251832	snp	A/G			intron-variant	ING4	GRCh38.p7	12:6662630	TCATCATCTGACAGT[A/G]GTCACTCATCACCAC	51147
rs781289916	snp	A/G	1.6486e-05	0.00287102	missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652765	TCTCCTTTTGAGTCC[A/G]GCCTTCTAGGGAAGA	51147
rs781440219	in-del	-/TTT			intron-variant	ING4	GRCh38.p7	12:6656172	TTTCTTTAATTCTTC[-/TTT]TTTTTTTTTTTTGAG	51147
rs781457492	snp	C/G			missense, nc-transcript-variant	ING4	GRCh38.p7	12:6652959	CCTTTGCTGGAAGAG[C/G]TGTCATAGTCACTTG	51147
rs781642535	snp	C/G	1.65996e-05	0.00288089	utr-variant-5-prime, upstream-variant-2KB	ING4	GRCh38.p7	12:6663125	AAAACAAAGCAACTT[C/G]CGATCCGCCCCGGAA	51147
rs796101268	snp	G/T			intron-variant	ING4	GRCh38.p7	12:6661110	TTTTGTTTTTGTTTT[G/T]TTTTTGAGGCGGAGT	51147
rs796371737	multinucleotide-polymorphism	CA/TG			intron-variant	ING4	GRCh38.p7	12:6657480	AACAAAAAATAAAGT[CA/TG]AGCTCAGTTTTCCTT	51147