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

PCGF1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1060782	snp	A/C	0	0	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504612	TCCTGTGGCCCCACT[A/C]CATTTGTTTTTTAGA	84759
rs2240442	snp	A/G	0.133435	0.221162	intron-variant	PCGF1	GRCh38.p7	2:74506646	TTTGGTAGGACTCAC[A/G]TAGGCAGAAGGCCAA	84759
rs2240443	snp	A/C	0.405732	0.19557	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505288	TTCAGACTCCCCCCA[A/C]CCATCCTACAGTCCT	84759
rs3192661	snp	C/T	8.61735e-05	0.00656348	intron-variant	PCGF1	GRCh38.p7	2:74507192	GGAAGGCGCACGGGT[C/T]GGGGTTTGAGGGTGG	84759
rs3806607	snp	A/G	0.493703	0.0557558	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508487	TTTTTAAGTACCCAG[A/G]GCCGGCGGTGTAGAG	84759
rs5024139	snp	A/C	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505085	AATAAAGCTGCAGTT[A/C]ATTTCACATAAATAT	84759
rs5024140	snp	A/T	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505091	GCTGCAGTTCATTTC[A/T]CATAAATATCTGGGG	84759
rs5024141	snp	C/T	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505092	CTGCAGTTCATTTCA[C/T]ATAAATATCTGGGGA	84759
rs5024143	snp	A/G	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505131	GAGTGGGATGGGGTG[A/G]GGGCTTGGCCCCTAC	84759
rs5024144	snp	C/T	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505135	GGGATGGGGTGGGGG[C/T]TTGGCCCCTACCTCC	84759
rs17010004	snp	C/G	0.148996	0.228688	intron-variant	PCGF1	GRCh38.p7	2:74507239	TCCTTCATCACACTA[C/G]ACGGCCAAGCCCCGC	84759
rs35595209	in-del	-/A			frameshift-variant, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506813	CAGTGGCTGTGTCTC[-/A]GTGGATCTTAATGTT	84759
rs41285989	snp	C/T	0.000494291	0.0157131	intron-variant	PCGF1	GRCh38.p7	2:74506164	GGGTCTTTACTGTCC[C/T]GCGGCCAAGGACATA	84759
rs41285991	snp	C/T	0.151251	0.229671	intron-variant	PCGF1	GRCh38.p7	2:74506707	AGTCCTCAAGAGGCC[C/T]CTCAAAGTCAGGTTG	84759
rs72818086	snp	G/T	0.00924125	0.0673441	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505365	AGCGGGAGAGCCATA[G/T]CTGCTTCATTGTCAT	84759
rs72818087	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506814	CAGTGGCTGTGTCTC[A/G]TGGATCTTAATGTTG	84759
rs73949674	snp	A/G	0.5	0	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509281	GAGCTTCCCTTTTCA[A/G]TCAGAATGAAAGTCA	84759
rs75600937	snp	A/C/G/T	0.0131133	0.0801018	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507861	AATTAAGGAGTGGGG[A/C/G/T]GGGGGGAGCACAGGG	84759
rs76022282	snp	C/G	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505108	ATAAATATCTGGGGA[C/G]GGAAGGGGAGTGGGA	84759
rs76860347	snp	A/C			splice-acceptor-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505420	AAAAAGGAGCTGCAC[A/C]TAGGAGGGAGATGGG	84759
rs77154120	snp	C/T	0.5	0	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505059	GCTTTTTAAAAGTTT[C/T]TATTTCAAAAAATAA	84759
rs77597989	snp	A/C/G	0.000129157	0.00803505	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505104	TCACATAAATATCTG[A/C/G]GGAGGGAAGGGGAGT	84759
rs77847000	snp	A/G	0.101315	0.20098	upstream-variant-2KB, missense, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505189	AAAAGCAAAGGGGAT[A/G]GCTAAGGAGAGAATG	84759
rs78352764	snp	C/G	0.5	0	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509444	AGGCTGCTGTAATCA[C/G]TCTAGATGAATAACA	84759
rs78921032	snp	C/T	0.300288	0.24489	missense, intron-variant	PCGF1	GRCh38.p7	2:74505997	TCATCATAGCGATAG[C/T]AGTGGGCTTTAGAGT	84759
rs79220597	snp	C/T	0.00886798	0.0659951	intron-variant	PCGF1	GRCh38.p7	2:74506926	AGGCCCTCTGGAAAC[C/T]GGATTCATGGGCTGG	84759
rs80278338	snp	C/T	0.0248432	0.108648	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507971	GCGAAAGACTGCCCC[C/T]TCCTACCCCCAAAGG	84759
rs111643889	snp	C/T	0.00993419	0.0697739	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508942	GGTCCGAGCCACTAT[C/T]ATCTGTCCTCTGTAG	84759
rs111794312	snp	C/T	0.5	0	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507609	CATCTTGTACACTGA[C/T]TGGAGCTGGTTCCGA	84759
rs112122276	snp	C/G	0.00263655	0.0362122	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505471	CTGGCAGGTCAAAAA[C/G]TACCCTGGTCCACCC	84759
rs113463685	snp	A/C			intron-variant	PCGF1	GRCh38.p7	2:74507152	CGAACCTCCTCCTGA[A/C]GATACACCCTCCGTC	84759
rs114370770	snp	A/G	0.0111196	0.0737302	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508032	GGTCGTCGGTCTTCT[A/G]TGACGACGACCCTGC	84759
rs115156451	snp	A/G	0.0119091	0.0762411	intron-variant	PCGF1	GRCh38.p7	2:74507242	TTCATCACACTAGAC[A/G]GCCAAGCCCCGCGCC	84759
rs116112081	snp	A/G	0.0655868	0.168795	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509676	TTTTTTTCCTCTGTT[A/G]TGTTCACAGATATAG	84759
rs116551748	snp	A/C	0.00914312	0.0669923	intron-variant	PCGF1	GRCh38.p7	2:74507256	CGGCCAAGCCCCGCG[A/C]CCTGCGCCATCAGCC	84759
rs117505699	snp	A/C/T	3.29697e-05	0.00406005	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505574	GGGTTTAGCATCAAG[A/C/T]GGTGACACAGGACCC	84759
rs117835471	snp	A/C	8.79159e-05	0.0066295	utr-variant-5-prime, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507673	GGAGACGCCATCTTA[A/C]AGGCTGATCCCAGCC	84759
rs138216462	snp	A/C	0.00636936	0.0560724	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507916	TGTAGAAATCATCAT[A/C]ATAGGCCCTACGCGA	84759
rs140632466	snp	A/G	0.000177226	0.00941179	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507624	CTGGAGCTGGTTCCG[A/G]AGCCTCATCGCGATC	84759
rs142233300	snp	C/G	0.000152805	0.00873951	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505312	GTCTGAAGGGGGTGT[C/G]ATCCCAGGGAGGGTG	84759
rs143031369	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508467	GCGGGGTGCTCGCTC[C/G]AGAGCTCTACACCGC	84759
rs143464189	snp	A/G	1.64895e-05	0.00287132	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505559	CTACTCACATGCTGA[A/G]GGTTTAGCATCAAGC	84759
rs143569594	snp	A/G	9.89266e-05	0.00703232	intron-variant	PCGF1	GRCh38.p7	2:74506912	AAAAGCAGATTCTCA[A/G]GCCCTCTGGAAACTG	84759
rs144121264	snp	C/T	1.64876e-05	0.00287116	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505567	ATGCTGAGGGTTTAG[C/T]ATCAAGCGGTGACAC	84759
rs144134701	snp	C/T	0.00027651	0.0117549	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505352	ACCTTGCCGAACCAG[C/T]GGGAGAGCCATATCT	84759
rs145551425	snp	C/G/T	0.00402715	0.0446924	intron-variant	PCGF1	GRCh38.p7	2:74505805	GGTTAGGGAATCCTA[C/G/T]CTTTCCTCCTCTTCC	84759
rs145617098	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507819	TGCTCACCTGAGCCC[C/T]ACCGGCCCCTCCCCT	84759
rs147573775	snp	C/T	5.10243e-05	0.0050507	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505228	GTAGTCAGTGGGGAA[C/T]GTTCTTATATTATTC	84759
rs148319271	snp	C/T	0.000798403	0.0199641	intron-variant	PCGF1	GRCh38.p7	2:74507468	GCGCACTGGGCACTC[C/T]GTCTCTGCGCAGGCG	84759
rs148848478	snp	C/T	0.000153988	0.00877328	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505404	GGAGAACTTCATTGT[C/T]AAAAAGGAGCTGCAC	84759
rs148881124	snp	C/T	0.00121947	0.0246627	intron-variant	PCGF1	GRCh38.p7	2:74505918	CTGGGTCATTGGCAC[C/T]GTCACCTCCTGCAAC	84759
rs149397277	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509478	CACCCACCCTTTCAC[C/T]TCCTTGCTCTTTTTT	84759
rs149582140	snp	C/T	0.00289716	0.0379498	missense, intron-variant	PCGF1	GRCh38.p7	2:74506202	CAGTGGGCTGGGTGA[C/T]CCGGTCCAAACCTCG	84759
rs150786268	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504896	GTTTCACACATATAG[A/G]GATCCTCTACCCTTC	84759
rs150874982	snp	A/C/T	0.000131836	0.008118	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505601	ACCCTCCGGAGATGG[A/C/T]GTACCTCAGCTCTAA	84759
rs180955861	snp	G/T	0.00993419	0.0697739	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508177	GCTTTGCAGAGTCTC[G/T]GAGAGGGTGCCGGGG	84759
rs181340250	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505482	AAAACTACCCTGGTC[C/T]ACCCTAGACTCTGTC	84759
rs181766336	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504675	TTATAAAACTATAAT[A/G]CAATTCTTTGGATTT	84759
rs182625168	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509249	GTTGTTCCTTTTTTA[C/T]GTTTAAAACCTGTTG	84759
rs182797844	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508878	CAAGAAGTTATGAGA[A/T]TAGTGATTAATCAAT	84759
rs183212992	snp	A/G			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508662	TGGTGAAATAGAAAG[A/G]ACGTGGAGGGGAATG	84759
rs184354450	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504858	ACCTTCCCATCACCA[A/G]AAAGAGTGGTGTGGG	84759
rs185419211	snp	C/T	3.30546e-05	0.00406524	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505522	TTAGCCCCTTCTCCC[C/T]CTCAAGAAACCTACT	84759
rs185950692	snp	A/G	3.29462e-05	0.00405857	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506038	GCTGAAGGGGAGGCC[A/G]AGGTTGCTCAGTGCT	84759
rs185950710	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508211	GGGGAGTGAGAGACC[C/T]CCAGGGACTTGGTAG	84759
rs187670961	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508668	AATAGAAAGGACGTG[G/T]AGGGGAATGACCAGA	84759
rs187882706	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509052	GATTCTGATAAAACA[C/T]GAAACACAAAGGACA	84759
rs188933540	snp	A/G	5.68037e-05	0.00532903	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505327	GATCCCAGGGAGGGT[A/G]GCCTGGCTTACCTTG	84759
rs190465152	snp	A/T			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504639	TAGACTTCTCCCTCC[A/T]TTTTGTCCCCATCCC	84759
rs190595537	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508866	GTGAATATGCAGCAA[C/G]AAGTTATGAGATTAG	84759
rs191140721	snp	C/T	0.00159617	0.0282053	intron-variant	PCGF1	GRCh38.p7	2:74506404	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAA	84759
rs191999052	snp	C/G	0.0115144	0.0749975	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508251	TCCCCCATTCTCCCC[C/G]CTGCTGCCGGGGATG	84759
rs192852437	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509075	AAAGGACAAAGGACA[A/G]TTTTTGAGATGTGGA	84759
rs199697372	snp	C/T	0.0515954	0.152104	missense, intron-variant	PCGF1	GRCh38.p7	2:74505973	CGCTCCAGGCACAGG[C/T]TCAACTGCTCATCAT	84759
rs200118363	snp	C/T	0.071262	0.174793	missense, intron-variant	PCGF1	GRCh38.p7	2:74506045	GGGAGGCCGAGGTTG[C/T]TCAGTGCTGGCTCTG	84759
rs200377150	snp	C/G	0.000165333	0.00909061	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505514	CTCCTTTCTTAGCCC[C/G]TTCTCCCCCTCAAGA	84759
rs200556348	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant	PCGF1	GRCh38.p7	2:74506048	AGGCCGAGGTTGCTC[A/G]GTGCTGGCTCTGAGA	84759
rs200641357	snp	G/T	0.280878	0.248086	missense, intron-variant	PCGF1	GRCh38.p7	2:74506000	TCATAGCGATAGTAG[G/T]GGGCTTTAGAGTGGT	84759
rs200678431	snp	A/G	0.0813875	0.18458	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74505977	CCAGGCACAGGTTCA[A/G]CTGCTCATCATAGCG	84759
rs200707864	snp	C/G	0.0610156	0.163661	missense, intron-variant	PCGF1	GRCh38.p7	2:74506049	GGCCGAGGTTGCTCA[C/G]TGCTGGCTCTGAGAA	84759
rs200862116	snp	A/G	0.000149245	0.00863714	intron-variant	PCGF1	GRCh38.p7	2:74506268	CTAGAAGAAGGTGAA[A/G]TATGAGAATAAAGTA	84759
rs200904086	snp	A/G			missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505614	GGCGTACCTCAGCTC[A/G]AACAGAACATCGGAC	84759
rs201019641	snp	A/G	2.00914e-05	0.00316943	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505467	CTTTCTGGCAGGTCA[A/G]AAACTACCCTGGTCC	84759
rs201054134	snp	A/C/G	4.94173e-05	0.00497053	missense, intron-variant	PCGF1	GRCh38.p7	2:74505992	ACTGCTCATCATAGC[A/C/G]ATAGTAGTGGGCTTT	84759
rs201312933	snp	C/T	3.31334e-05	0.00407009	intron-variant	PCGF1	GRCh38.p7	2:74505816	CCTATCTTTCCTCCT[C/T]TTCCCCACCCAGAGC	84759
rs201383050	snp	C/T	0.00199804	0.031544	missense, intron-variant	PCGF1	GRCh38.p7	2:74505958	TCTCCTCACCTCAGC[C/T]GCTCCAGGCACAGGT	84759
rs201559196	snp	A/G/T	7.45666e-05	0.00610555	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505353	CCTTGCCGAACCAGC[A/G/T]GGAGAGCCATATCTG	84759
rs201679071	snp	A/G	0.000560113	0.0167255	intron-variant	PCGF1	GRCh38.p7	2:74506149	AAGAAGAATGCTCTG[A/G]GGTCTTTACTGTCCC	84759
rs201836803	snp	A/G	3.29919e-05	0.00406138	missense, intron-variant	PCGF1	GRCh38.p7	2:74506219	CGGTCCAAACCTCGG[A/G]ACTGGTAGAATTCCC	84759
rs201906065	snp	A/C	0.000527313	0.0162289	intron-variant	PCGF1	GRCh38.p7	2:74506897	AGACTGCAGGAAAAG[A/C]AAAGCAGATTCTCAG	84759
rs202099071	snp	A/C	0.00339088	0.0410358	intron-variant	PCGF1	GRCh38.p7	2:74507559	CGACCACAGCAGTAA[A/C]CCTGCCGCCCTTGCA	84759
rs202141276	snp	A/C/G	1.64789e-05	0.0028704	intron-variant	PCGF1	GRCh38.p7	2:74505671	AGGGAAGAGGGCAAG[A/C/G]TGTGTGAGGGAAGGA	84759
rs368170536	snp	A/C/G	0.000769544	0.0196005	intron-variant	PCGF1	GRCh38.p7	2:74507197	CTCAAACCCCAACCC[A/C/G]TGCGCCTTCCCACCT	84759
rs368396183	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504592	AAGCCTCCATTTCTG[A/G]CAATTCCTGTGGCCC	84759
rs368528693	snp	A/G	3.30202e-05	0.00406313	intron-variant	PCGF1	GRCh38.p7	2:74506935	GGAAACTGGATTCAT[A/G]GGCTGGGTGGGGTGC	84759
rs368548736	snp	C/T	1.64795e-05	0.00287045	intron-variant	PCGF1	GRCh38.p7	2:74506144	TGGGCAAGAAGAATG[C/T]TCTGGGGTCTTTACT	84759
rs369013269	snp	A/G	8.23988e-05	0.00641815	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505602	CCCTCCGGAGATGGC[A/G]TACCTCAGCTCTAAC	84759
rs369110833	snp	A/G	0.000181259	0.00951824	intron-variant	PCGF1	GRCh38.p7	2:74506165	GGTCTTTACTGTCCC[A/G]CGGCCAAGGACATAC	84759
rs369200306	snp	A/G	0.000153988	0.00877328	upstream-variant-2KB, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505167	CTTCTCTTTCACACT[A/G]TATTGTAAAAGCAAA	84759
rs369371639	snp	C/T	4.37646e-05	0.00467765	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505432	CACCTAGGAGGGAGA[C/T]GGGGGCATAATTTTA	84759
rs369563912	in-del	-/C			frameshift-variant, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505352	ACCTTGCCGAACCAG[-/C]GGGAGAGCCATATCT	84759
rs369860290	snp	C/T	0.00398564	0.0444627	intron-variant	PCGF1	GRCh38.p7	2:74507470	GCACTGGGCACTCTG[C/T]CTCTGCGCAGGCGCA	84759
rs369972519	snp	C/T	1.65116e-05	0.00287324	missense, intron-variant	PCGF1	GRCh38.p7	2:74506234	GACTGGTAGAATTCC[C/T]GAATCCGTTTCTCTT	84759
rs370057778	snp	A/C			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509682	TCCTCTGTTGTGTTC[A/C]CAGATATAGCTCCAG	84759
rs370306832	snp	A/C	0.000148337	0.00861085	intron-variant	PCGF1	GRCh38.p7	2:74505934	GTCACCTCCTGCAAC[A/C]CCTGACCTTCTCCTC	84759
rs370330617	snp	A/G			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509083	AAGGACAATTTTTGA[A/G]ATGTGGATATGTTTA	84759
rs370613426	snp	G/T			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508158	CACGGAGGGAGTTTC[G/T]TGGGCTTTGCAGAGT	84759
rs370641896	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506780	TGTCCTGCATGACCC[A/G]GTCCAGTTTGAGGTT	84759
rs370764527	snp	A/G	1.64961e-05	0.00287189	intron-variant	PCGF1	GRCh38.p7	2:74505907	CCTCCCTGGCTCTGG[A/G]TCATTGGCACTGTCA	84759
rs370782718	snp	A/G	1.65053e-05	0.0028727	intron-variant	PCGF1	GRCh38.p7	2:74507011	TGAAGACTAGGGACT[A/G]GAAGAACTAGGCAGT	84759
rs371438909	snp	C/T	3.29609e-05	0.00405948	intron-variant	PCGF1	GRCh38.p7	2:74506166	GTCTTTACTGTCCCG[C/T]GGCCAAGGACATACC	84759
rs371588004	snp	C/T	0.000153988	0.00877328	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505501	CTAGACTCTGTCCCT[C/T]CTTTCTTAGCCCCTT	84759
rs371826799	snp	C/G	0.00517822	0.0506191	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504648	CCCTCCTTTTTGTCC[C/G]CATCCCCCAAGTTAT	84759
rs372094024	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505305	GGGGGGAGTCTGAAG[A/G]GGGTGTGATCCCAGG	84759
rs372394478	snp	A/G	6.59163e-05	0.00574054	intron-variant	PCGF1	GRCh38.p7	2:74505696	GAAGGACCATGGGAG[A/G]TGAGTCTCCTTAGAG	84759
rs372441266	snp	C/T	0.000206058	0.0101482	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505238	GGGAATGTTCTTATA[C/T]TATTCAAAGGGCCCC	84759
rs372719465	snp	A/G	4.94254e-05	0.00497094	intron-variant	PCGF1	GRCh38.p7	2:74506060	CTCAGTGCTGGCTCT[A/G]AGAAAGATAGGGTAG	84759
rs373215549	snp	C/G	0.00279242	0.0372774	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507862	ATTAAGGAGTGGGGG[C/G]GGGGGAGCACAGGGA	84759
rs373268971	snp	C/T	0.000744078	0.019274	intron-variant	PCGF1	GRCh38.p7	2:74505806	GTTAGGGAATCCTAT[C/T]TTTCCTCCTCTTCCC	84759
rs373985062	snp	C/G/T	4.94428e-05	0.00497186	intron-variant	PCGF1	GRCh38.p7	2:74506710	CCTCAAGAGGCCCCT[C/G/T]AAAGTCAGGTTGGTG	84759
rs374254649	snp	A/C	3.29804e-05	0.00406068	intron-variant	PCGF1	GRCh38.p7	2:74507035	AGGCAGTCTCCAAGG[A/C]ACTCACAAGTATGAA	84759
rs374375582	snp	C/T	3.2956e-05	0.00405918	intron-variant	PCGF1	GRCh38.p7	2:74506100	TGGTGGCACACATTC[C/T]ATACTCCTCTTTCCC	84759
rs374604995	snp	A/G			intron-variant	PCGF1	GRCh38.p7	2:74507015	GACTAGGGACTGGAA[A/G]AACTAGGCAGTCTCC	84759
rs374668190	in-del	-/TAGCTTGTCGAACCAG			upstream-variant-2KB, frameshift-variant, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505187	TAAAAGCAAAGGGGA[-/TAGCTTGTCGAACCAG]TGGCTAAGGAGAGAA	84759
rs374826116	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506008	ATAGTAGTGGGCTTT[A/G]GAGTGGTCAAAGCTG	84759
rs374883883	snp	A/G/T	3.30111e-05	0.00406259	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505535	CCCCTCAAGAAACCT[A/G/T]CTGTGGGACTACTCA	84759
rs375026309	snp	C/T	4.94645e-05	0.00497291	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505745	TTCTCACCTGCAGGA[C/T]GCTTTTATTCTTGTC	84759
rs375083490	snp	A/G	0.0023933	0.0345097	intron-variant	PCGF1	GRCh38.p7	2:74506376	AAGTCAGGAGATTGA[A/G]GCCATCCTGGCTAAC	84759
rs375266773	snp	C/T	0.00048873	0.0156245	intron-variant	PCGF1	GRCh38.p7	2:74506292	TAAAGTATTAGCCCT[C/T]CGGGGCCGGGCGCGG	84759
rs375839492	snp	A/G	1.64795e-05	0.00287045	intron-variant	PCGF1	GRCh38.p7	2:74506173	CTGTCCCGCGGCCAA[A/G]GACATACCTTCCCCA	84759
rs376421770	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504654	TTTTTGTCCCCATCC[C/T]CCAAGTTATAAAACT	84759
rs376879850	snp	A/G	0.000153988	0.00877328	intron-variant	PCGF1	GRCh38.p7	2:74506704	ATTAGTCCTCAAGAG[A/G]CCCCTCAAAGTCAGG	84759
rs376945133	snp	G/T	4.94605e-05	0.0049727	intron-variant	PCGF1	GRCh38.p7	2:74506907	AAAAGAAAAGCAGAT[G/T]CTCAGGCCCTCTGGA	84759
rs376977193	snp	A/C/G	4.9442e-05	0.00497182	intron-variant	PCGF1	GRCh38.p7	2:74505700	GACCATGGGAGGTGA[A/C/G]TCTCCTTAGAGAGGC	84759
rs377197816	snp	C/G/T	0.00119737	0.0244387	intron-variant	PCGF1	GRCh38.p7	2:74507329	AGAGGGCTCCGCGCA[C/G/T]AGCGGGGGCTTCCCT	84759
rs377297689	snp	C/T	1.65814e-05	0.00287931	intron-variant	PCGF1	GRCh38.p7	2:74505821	CTTTCCTCCTCTTCC[C/T]CACCCAGAGCCATGA	84759
rs377327714	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507863	TTAAGGAGTGGGGGG[A/G]GGGGAGCACAGGGAA	84759
rs377496136	snp	C/T			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509012	TTCTCAACATCACAG[C/T]TGAGTGCTGTTTCTC	84759
rs377509940	snp	A/G	1.64866e-05	0.00287106	intron-variant	PCGF1	GRCh38.p7	2:74505922	GTCATTGGCACTGTC[A/G]CCTCCTGCAACCCCT	84759
rs377600929	snp	A/C/G	3.29484e-05	0.00405871	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506742	CTCACTGTCTTGCAA[A/C/G]CCAGGCACCAGCTTA	84759
rs528385530	snp	A/G	6.76396e-05	0.00581508	intron-variant	PCGF1	GRCh38.p7	2:74506294	AAGTATTAGCCCTTC[A/G]GGGCCGGGCGCGGTG	84759
rs529569986	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507859	GTAATTAAGGAGTGG[C/G]GGGGGGGGAGCACAG	84759
rs529586668	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508432	AGTAGCATAGGCCCA[A/G]TCCCGCACTTGGGGA	84759
rs529943694	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504758	AGCCTTCTCACCACC[A/G]CTGAATTAGGAAACC	84759
rs530133603	snp	A/C	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74506390	AGGCCATCCTGGCTA[A/C]CATGGTGAAACCCCG	84759
rs530845611	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504819	TGCAGCATACAAAGA[C/T]AGCTGAGAGCTCCCC	84759
rs531105433	snp	A/G	0.00636936	0.0560724	intron-variant	PCGF1	GRCh38.p7	2:74506522	GGTGGAGCTTGCAGT[A/G]AGCTGAGATTGCGCC	84759
rs531194935	snp	A/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508450	CCGCACTTGGGGACT[A/G]CGCGGGGTGCTCGCT	84759
rs532396922	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505491	CTGGTCCACCCTAGA[C/T]TCTGTCCCTCCTTTC	84759
rs532739027	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508618	GGGACTTTGGGCACA[A/T]TTTAGACTTGGGGGA	84759
rs533815306	snp	A/G	0.000152614	0.00873404	intron-variant	PCGF1	GRCh38.p7	2:74507538	GCCCCAATTCGCACC[A/G]CTGGCCGACCACAGC	84759
rs534941047	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504644	TTCTCCCTCCTTTTT[A/G]TCCCCATCCCCCAAG	84759
rs535182655	snp	C/G	0.00119737	0.0244387	intron-variant	PCGF1	GRCh38.p7	2:74506599	AAGAATAAAGTATTA[C/G]CCCTTCCTCACTTTT	84759
rs535218433	in-del	-/GGT			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507859	TAATTAAGGAGTGGG[-/GGT]GGGGGGGGAGCACAG	84759
rs535342947	snp	G/T	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74506562	CAGCCTGGGCAAGAC[G/T]CCGTCTCAAAAAAAG	84759
rs536048118	snp	A/C			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508573	GAGAGATTCCAATGG[A/C]GACCTCAAAAAAGGC	84759
rs536417881	snp	C/T	0.000102717	0.00716574	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505241	AATGTTCTTATATTA[C/T]TCAAAGGGCCCCTCA	84759
rs537751722	snp	C/G/T	0.00032172	0.0126796	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505291	ACTGTAGGATGGTTG[C/G/T]GGGGAGTCTGAAGGG	84759
rs538735554	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504939	ACATTGAGGGCCCAT[A/G]GCCATAGAGGACAGG	84759
rs539212299	snp	A/G	0.000798403	0.0199641	intron-variant	PCGF1	GRCh38.p7	2:74506647	TGGCCTTCTGCCTAC[A/G]TGAGTCCTACCAAAC	84759
rs539304585	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508010	TCTGTGCCCGCTACC[C/G]GCTCAGGGTCGTCGG	84759
rs539806471	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508960	CTGTCCTCTGTAGTG[G/T]CCTCTTGACTGTTTT	84759
rs540778017	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508368	AGGAGGAGGGGAGGA[C/T]GACTAGGACACTGCC	84759
rs540907249	snp	G/T			intron-variant	PCGF1	GRCh38.p7	2:74506316	GGCGCGGTGGCTCAC[G/T]CCTGTAATCCCAGCA	84759
rs540985608	snp	C/G	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74506329	ACGCCTGTAATCCCA[C/G]CACTTTGGGAGGCAG	84759
rs541622259	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505465	AACTTTCTGGCAGGT[C/T]AAAAACTACCCTGGT	84759
rs541880972	snp	A/G	4.94752e-05	0.00497344	intron-variant	PCGF1	GRCh38.p7	2:74506920	ATTCTCAGGCCCTCT[A/G]GAAACTGGATTCATG	84759
rs542166520	snp	C/T	6.44808e-05	0.0056777	intron-variant	PCGF1	GRCh38.p7	2:74507569	AGTAACCCTGCCGCC[C/T]TTGCACCTCGTTCCG	84759
rs542685338	in-del	-/T	0.00636936	0.0560724	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505046	GCAGAAGAGAGGTGC[-/T]TTTTAAAAGTTTTTA	84759
rs543082188	snp	A/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508267	CTGCTGCCGGGGATG[A/G]GGGGGGCAGGCCCTG	84759
rs544029987	in-del	-/A	0.000529429	0.0162614	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505466	ACTTTCTGGCAGGTC[-/A]AAAACTACCCTGGTC	84759
rs544882194	snp	A/G			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509630	TCATCTGCCTTTTCC[A/G]CTAGACTATAAGCTT	84759
rs545095758	in-del	-/A	0.00279162	0.0372561	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508579	TCCAATGGAGACCTC[-/A]AAAAAAGGCTTTCTG	84759
rs546362148	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507792	CCCCGCCCACGTCCC[A/T]TTCTCCCTGTGTGCT	84759
rs546898283	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507844	TCCCCTGCTCAATCC[G/T]TAATTAAGGAGTGGG	84759
rs547517029	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504993	AGGATTTTTGAAGAA[A/G]GCAGGACACAGCATG	84759
rs548389788	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504786	ACCTCCTAAGAGGCC[C/T]GCACCCGCACTGTAT	84759
rs548446132	snp	G/T	4.9458e-05	0.00497258	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505742	CCCTTCTCACCTGCA[G/T]GACGCTTTTATTCTT	84759
rs549159911	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508748	GGCCATAAAGAGTTG[C/T]GATTTTTAGCCTGAG	84759
rs549441945	snp	C/G/T	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74507373	CTGACCCTCCTTTCC[C/G/T]AGGGGAGACTACACA	84759
rs550318530	snp	A/G	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74507391	GGGAGACTACACAAC[A/G]TCGGCGACACAACGC	84759
rs550978053	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508637	AGACTTGGGGGAGGG[A/G]GTGGAAGTGTGGTGA	84759
rs552819855	snp	C/T	0.000798403	0.0199641	intron-variant	PCGF1	GRCh38.p7	2:74506534	AGTGAGCTGAGATTG[C/T]GCCACTGCACTCCAG	84759
rs553003515	snp	C/T	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74506564	GCCTGGGCAAGACTC[C/T]GTCTCAAAAAAAGAA	84759
rs553016148	snp	C/T	0.000280004	0.0118289	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74505975	CTCCAGGCACAGGTT[C/T]AACTGCTCATCATAG	84759
rs553621448	in-del	-/TGC			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504800	CGCACCCGCACTGTA[-/TGC]TGCTGCAGCATACAA	84759
rs553991008	in-del	-/GAG	0.00159617	0.0282053	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504946	GGGCCCATGGCCATA[-/GAG]GACAGGCCCTTCTTC	84759
rs555160404	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505282	CCCCTGAGGACTGTA[A/G]GATGGTTGGGGGGAG	84759
rs555609670	snp	A/C	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74507544	ATTCGCACCGCTGGC[A/C]GACCACAGCAGTAAC	84759
rs555919288	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509322	GTGGTGTGCAAGGGC[C/T]TGCATAGTCTCTTCA	84759
rs556865925	snp	C/T	1.6477e-05	0.00287024	intron-variant	PCGF1	GRCh38.p7	2:74506098	GCTGGTGGCACACAT[C/T]CCATACTCCTCTTTC	84759
rs557045030	snp	C/T	0.000798403	0.0199641	intron-variant	PCGF1	GRCh38.p7	2:74506618	TTCCTCACTTTTTGT[C/T]CTTCCCTCATCTTTG	84759
rs557316843	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508058	CCTGCTGAAGAAGCC[C/T]CTCCTGGGTCCTCTC	84759
rs557525086	snp	A/C	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74507506	CGCCCGGCCAGCCAC[A/C]GCCCGTCCTTTAGCC	84759
rs557539325	snp	C/T	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74506671	ACCAAACCCGTCACC[C/T]CAAGCTGCCACTCAG	84759
rs557708040	snp	A/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508153	GGCTTCACGGAGGGA[A/G]TTTCTTGGGCTTTGC	84759
rs559090590	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509354	ATACACCAGGATATC[C/T]TTCCACTGTGTCCCC	84759
rs559127824	snp	A/G			intron-variant	PCGF1	GRCh38.p7	2:74506555	TGCACTCCAGCCTGG[A/G]CAAGACTCCGTCTCA	84759
rs562145094	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508387	TAGGACACTGCCACA[C/G]ACAGACAGGCTTAGG	84759
rs562287994	snp	C/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508163	AGGGAGTTTCTTGGG[C/G]TTTGCAGAGTCTCGG	84759
rs562370545	snp	G/T	0.00279162	0.0372561	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507857	CCGTAATTAAGGAGT[G/T]GGGGGGGGGGAGCAC	84759
rs562808565	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509623	TAGTTTTTCATCTGC[C/T]TTTTCCACTAGACTA	84759
rs563403769	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504792	TAAGAGGCCCGCACC[C/T]GCACTGTATGCTGCA	84759
rs564275851	snp	A/G			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508711	CAAGATGTAGATTTG[A/G]GAGTGGTAATAGAAA	84759
rs564656525	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507795	CGCCCACGTCCCTTT[A/C]TCCCTGTGTGCTCAC	84759
rs564918282	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505486	CTACCCTGGTCCACC[C/T]TAGACTCTGTCCCTC	84759
rs566191847	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508664	GTGAAATAGAAAGGA[C/G]GTGGAGGGGAATGAC	84759
rs567390907	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508804	TTGAAGGGAGGTTAT[A/C]CTGTGAAAGCGACAT	84759
rs567695520	snp	A/G			intron-variant	PCGF1	GRCh38.p7	2:74507452	GATCGCAACCACGCA[A/G]GCGCACTGGGCACTC	84759
rs567939358	snp	C/T	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74507347	CGGGGGCTTCCCTCA[C/T]GTGGACTCGCCTGAC	84759
rs568090394	snp	A/C	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74506576	CTCCGTCTCAAAAAA[A/C]GAAAAAAAAGAATAA	84759
rs568783240	snp	C/T	0.00557542	0.0525036	intron-variant	PCGF1	GRCh38.p7	2:74507344	CAGCGGGGGCTTCCC[C/T]CACGTGGACTCGCCT	84759
rs570129431	snp	C/T	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74506408	TGGTGAAACCCCGTC[C/T]CTACTAAAAAATATA	84759
rs571120692	snp	C/G	0.000399281	0.0141238	intron-variant	PCGF1	GRCh38.p7	2:74506544	GATTGCGCCACTGCA[C/G]TCCAGCCTGGGCAAG	84759
rs571351842	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504889	AGGCCTGGTTTCACA[A/C]ATATAGGGATCCTCT	84759
rs572536377	snp	A/G			synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74505999	ATCATAGCGATAGTA[A/G]TGGGCTTTAGAGTGG	84759
rs572740229	snp	C/T	7.7003e-05	0.00620448	intron-variant	PCGF1	GRCh38.p7	2:74507525	CGTCCTTTAGCCCGC[C/T]CCAATTCGCACCGCT	84759
rs573699624	snp	A/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508569	AAGGGAGAGATTCCA[A/G]TGGAGACCTCAAAAA	84759
rs574404816	snp	C/T	6.58913e-05	0.00573945	missense, intron-variant	PCGF1	GRCh38.p7	2:74506037	TGCTGAAGGGGAGGC[C/T]GAGGTTGCTCAGTGC	84759
rs574493633	snp	C/T	2.24162e-05	0.00334778	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505401	CAGGGAGAACTTCAT[C/T]GTCAAAAAGGAGCTG	84759
rs575175723	snp	A/C			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504913	ATCCTCTACCCTTCT[A/C]CTTTGGCAAGACATT	84759
rs575744866	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508135	GATGGCGGGTCTTCT[C/G]CCGGCTTCACGGAGG	84759
rs576948817	snp	A/G	0.000174019	0.00932626	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505324	TGTGATCCCAGGGAG[A/G]GTGGCCTGGCTTACC	84759
rs577440951	snp	C/T			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509432	TCTTTACTCATGAGG[C/T]TGCTGTAATCACTCT	84759
rs577882947	in-del	-/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507857	CCGTAATTAAGGAGT[-/G]GGGGGGGGGGAGCAC	84759
rs745541752	snp	A/G	0.000181466	0.00952365	intron-variant	PCGF1	GRCh38.p7	2:74505905	ACCCTCCCTGGCTCT[A/G]GGTCATTGGCACTGT	84759
rs745821405	in-del	-/G	3.31268e-05	0.00406968	intron-variant	PCGF1	GRCh38.p7	2:74506261	CTTCACCTAGAAGAA[-/G]GGTGAAGTATGAGAA	84759
rs745924671	snp	A/G	1.64819e-05	0.00287066	missense, intron-variant	PCGF1	GRCh38.p7	2:74506189	GACATACCTTCCCCA[A/G]TGGGCTGGGTGACCC	84759
rs746009674	snp	A/G	1.64754e-05	0.00287009	intron-variant	PCGF1	GRCh38.p7	2:74506080	AGATAGGGTAGTGAG[A/G]TGGCTGGTGGCACAC	84759
rs746050308	snp	A/C			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509280	AGAGCTTCCCTTTTC[A/C]ATCAGAATGAAAGTC	84759
rs746215351	snp	G/T	0.000299909	0.0122419	synonymous-codon, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505375	CCATATCTGCTTCAT[G/T]GTCATGTGATCAGGG	84759
rs746299694	snp	A/G			intron-variant	PCGF1	GRCh38.p7	2:74506581	TCTCAAAAAAAGAAA[A/G]AAAAGAATAAAGTAT	84759
rs746312055	snp	A/C	2.25329e-05	0.00335648	intron-variant	PCGF1	GRCh38.p7	2:74507196	CCTCAAACCCCAACC[A/C]GTGCGCCTTCCCACC	84759
rs746382376	snp	G/T	4.94882e-05	0.0049741	intron-variant	PCGF1	GRCh38.p7	2:74507026	GGAAGAACTAGGCAG[G/T]CTCCAAGGCACTCAC	84759
rs746502179	snp	C/G			intron-variant	PCGF1	GRCh38.p7	2:74507522	GCCCGTCCTTTAGCC[C/G]GCCCCAATTCGCACC	84759
rs746662646	snp	A/C	1.64868e-05	0.00287109	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505568	TGCTGAGGGTTTAGC[A/C]TCAAGCGGTGACACA	84759
rs746746412	snp	C/T	9.77756e-05	0.0069913	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507707	CACTTCCGGTGCCGC[C/T]TGCAGGGCGGGACTT	84759
rs746842728	in-del	-/CCCTAGACTCTGTCCCTCCTTTCTTAGCCCCTTC	1.65026e-05	0.00287246	intron-variant	PCGF1	GRCh38.p7	2:74506933	TGGAAACTGGATTCA[lengthTooLong]TGGGCTGGGTGGGGT	84759
rs746970679	snp	A/G			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509250	TTGTTCCTTTTTTAC[A/G]TTTAAAACCTGTTGA	84759
rs746978198	snp	C/T	3.3173e-05	0.00407252	intron-variant	PCGF1	GRCh38.p7	2:74506269	TAGAAGAAGGTGAAG[C/T]ATGAGAATAAAGTAT	84759
rs747261980	snp	A/G	3.12534e-05	0.00395294	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505306	GGGGGAGTCTGAAGG[A/G]GGTGTGATCCCAGGG	84759
rs747351827	snp	A/G	1.65214e-05	0.0028741	intron-variant	PCGF1	GRCh38.p7	2:74506994	GCTGGCAGTCAGCTT[A/G]GTGAAGACTAGGGAC	84759
rs747355890	snp	A/G	4.98128e-05	0.00499038	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505126	AAGGGGAGTGGGATG[A/G]GGTGGGGGCTTGGCC	84759
rs747441614	snp	A/G	8.23703e-05	0.00641704	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506838	AATGTTGCACATGGG[A/G]CAGTACTTGCTAGTT	84759
rs747452489	in-del	-/AT			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508750	CCATAAAGAGTTGCG[-/AT]TTTTAGCCTGAGGGC	84759
rs747527717	snp	C/T			intron-variant	PCGF1	GRCh38.p7	2:74506393	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	84759
rs747614689	snp	C/T			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509161	ACTTATCAAATTGTA[C/T]ACTTCAAATATTTGC	84759
rs747632913	snp	G/T	1.64904e-05	0.00287139	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505556	GGACTACTCACATGC[G/T]GAGGGTTTAGCATCA	84759
rs747814369	snp	C/T	7.31716e-05	0.00604818	intron-variant	PCGF1	GRCh38.p7	2:74507548	GCACCGCTGGCCGAC[C/T]ACAGCAGTAACCCTG	84759
rs747888638	snp	C/T			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508062	CTGAAGAAGCCCCTC[C/T]TGGGTCCTCTCCTCG	84759
rs748217607	in-del	-/CTC	6.59141e-05	0.00574045	intron-variant	PCGF1	GRCh38.p7	2:74505944	GCAACCCCTGACCTT[-/CTC]CTCACCTCAGCCGCT	84759
rs748252976	snp	A/G	6.05089e-05	0.00550007	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505117	TGGGGAGGGAAGGGG[A/G]GTGGGATGGGGTGGG	84759
rs748342812	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506809	TTGAGCAGTGGCTGT[A/G]TCTCGTGGATCTTAA	84759
rs748517556	snp	C/T	1.69075e-05	0.00290748	intron-variant	PCGF1	GRCh38.p7	2:74506293	AAAGTATTAGCCCTT[C/T]GGGGCCGGGCGCGGT	84759
rs748685316	snp	A/G	1.64781e-05	0.00287033	intron-variant	PCGF1	GRCh38.p7	2:74505653	TCTGGGAGCAGGGAG[A/G]GGAGGGAAGAGGGCA	84759
rs748765522	snp	A/C	7.71099e-05	0.00620879	intron-variant	PCGF1	GRCh38.p7	2:74507527	TCCTTTAGCCCGCCC[A/C]AATTCGCACCGCTGG	84759
rs748975225	snp	A/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507775	GCTCACCCTCTGTAA[A/G]GCCCCGCCCACGTCC	84759
rs749070897	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506047	GAGGCCGAGGTTGCT[C/T]AGTGCTGGCTCTGAG	84759
rs749396207	snp	A/C	1.66463e-05	0.00288494	intron-variant	PCGF1	GRCh38.p7	2:74506280	GAAGTATGAGAATAA[A/C]GTATTAGCCCTTCGG	84759
rs749540843	snp	A/G	1.64866e-05	0.00287106	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506206	GGGCTGGGTGACCCG[A/G]TCCAAACCTCGGGAC	84759
rs749738104	snp	C/T	1.64963e-05	0.00287192	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505544	AAACCTACTGTGGGA[C/T]TACTCACATGCTGAG	84759
rs750216797	snp	C/G	2.81797e-05	0.00375354	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505329	TCCCAGGGAGGGTGG[C/G]CTGGCTTACCTTGCC	84759
rs750363482	snp	A/C	1.64906e-05	0.00287142	intron-variant	PCGF1	GRCh38.p7	2:74506922	TCTCAGGCCCTCTGG[A/C]AACTGGATTCATGGG	84759
rs750605286	snp	C/T	1.64798e-05	0.00287047	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505603	CCTCCGGAGATGGCG[C/T]ACCTCAGCTCTAACA	84759
rs750716014	snp	C/G			intron-variant	PCGF1	GRCh38.p7	2:74507448	ACCCGATCGCAACCA[C/G]GCAGGCGCACTGGGC	84759
rs750732076	snp	C/G	6.98251e-05	0.00590827	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507647	TCGCGATCGCAATCT[C/G]GCCCCCCTGAGGAGA	84759
rs750956649	in-del	-/TTC	0.000253184	0.0112485	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505230	AGTCAGTGGGGAATG[-/TTC]TTATATTATTCAAAG	84759
rs750958240	snp	G/T			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508799	CTTTTTTGAAGGGAG[G/T]TTATCCTGTGAAAGC	84759
rs751136062	snp	G/T			intron-variant	PCGF1	GRCh38.p7	2:74507378	CCTCCTTTCCCAGGG[G/T]AGACTACACAACGTC	84759
rs751215052	snp	A/G	9.9965e-05	0.00706912	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505223	AAGTAGTAGTCAGTG[A/G]GGAATGTTCTTATAT	84759
rs751342958	snp	C/T	1.64882e-05	0.00287121	intron-variant	PCGF1	GRCh38.p7	2:74506910	AGAAAAGCAGATTCT[C/T]AGGCCCTCTGGAAAC	84759
rs751751799	snp	A/C			intron-variant	PCGF1	GRCh38.p7	2:74507327	GCAGAGGGCTCCGCG[A/C]ACAGCGGGGGCTTCC	84759
rs751861491	snp	C/T	0.000177069	0.00940762	intron-variant	PCGF1	GRCh38.p7	2:74507180	GTCACCAATCATCCA[C/T]CCTCAAACCCCAACC	84759
rs752140664	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506020	TTTAGAGTGGTCAAA[A/G]CTGCTGAAGGGGAGG	84759
rs752522803	snp	A/G	3.31417e-05	0.00407059	intron-variant	PCGF1	GRCh38.p7	2:74506263	TTCACCTAGAAGAAG[A/G]TGAAGTATGAGAATA	84759
rs752807806	snp	C/T	1.79661e-05	0.00299712	intron-variant	PCGF1	GRCh38.p7	2:74507155	ACCTCCTCCTGAAGA[C/T]ACACCCTCCGTCACC	84759
rs752894891	snp	C/T	1.64993e-05	0.00287218	intron-variant	PCGF1	GRCh38.p7	2:74506931	CTCTGGAAACTGGAT[C/T]CATGGGCTGGGTGGG	84759
rs753144657	snp	C/T	1.65312e-05	0.00287495	intron-variant	PCGF1	GRCh38.p7	2:74505801	CACAGGTTAGGGAAT[C/T]CTATCTTTCCTCCTC	84759
rs753369148	in-del	-/AGGGA	6.3806e-05	0.00564791	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505107	CATAAATATCTGGGG[-/AGGGA]AGGGGAGTGGGATGG	84759
rs753479974	snp	C/T	1.65081e-05	0.00287293	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506230	TCGGGACTGGTAGAA[C/T]TCCCGAATCCGTTTC	84759
rs753578073	snp	A/G	1.64792e-05	0.00287042	intron-variant	PCGF1	GRCh38.p7	2:74506160	TCTGGGGTCTTTACT[A/G]TCCCGCGGCCAAGGA	84759
rs753758472	snp	C/T	2.61073e-05	0.00361289	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505344	CCTGGCTTACCTTGC[C/T]GAACCAGCGGGAGAG	84759
rs753936073	snp	A/C	1.64738e-05	0.00286995	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506777	CGATGTCCTGCATGA[A/C]CCGGTCCAGTTTGAG	84759
rs754073484	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505067	AAAGTTTTTATTTCA[A/G]AAAATAAAGCTGCAG	84759
rs754127411	snp	A/C	8.24899e-05	0.00642169	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505765	TTATTCTTGTCTTTG[A/C]CAGAACTGGGGGGAA	84759
rs754141788	snp	C/T	1.64795e-05	0.00287045	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505633	AGAACATCGGACATA[C/T]TTGTTCTGGGAGCAG	84759
rs754215376	snp	C/T			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508903	ATCAATTATTCGTTA[C/T]AGCCCCTGTTTACCT	84759
rs754369775	snp	A/C	7.59273e-05	0.006161	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507654	CGCAATCTGGCCCCC[A/C]TGAGGAGACGCCATC	84759
rs754429398	snp	G/T	1.71764e-05	0.00293051	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507655	GCAATCTGGCCCCCC[G/T]GAGGAGACGCCATCT	84759
rs755002821	snp	A/C	6.55458e-05	0.00572439	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505101	ATTTCACATAAATAT[A/C]TGGGGAGGGAAGGGG	84759
rs755056669	snp	A/G	4.94205e-05	0.0049707	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506781	GTCCTGCATGACCCG[A/G]TCCAGTTTGAGGTTG	84759
rs755166777	in-del	-/GGGAG	1.64787e-05	0.00287038	intron-variant	PCGF1	GRCh38.p7	2:74505648	CTTGTTCTGGGAGCA[-/GGGAG]GGGAGGGAAGAGGGC	84759
rs755387225	snp	A/T	8.23906e-05	0.00641783	intron-variant	PCGF1	GRCh38.p7	2:74505644	CATACTTGTTCTGGG[A/T]GCAGGGAGGGGAGGG	84759
rs755437056	snp	A/G	4.9476e-05	0.00497348	synonymous-codon, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505552	TGTGGGACTACTCAC[A/G]TGCTGAGGGTTTAGC	84759
rs755737925	snp	A/T	3.29571e-05	0.00405924	intron-variant	PCGF1	GRCh38.p7	2:74506152	AAGAATGCTCTGGGG[A/T]CTTTACTGTCCCGCG	84759
rs756131238	snp	A/T	6.63636e-05	0.00575998	intron-variant	PCGF1	GRCh38.p7	2:74506271	GAAGAAGGTGAAGTA[A/T]GAGAATAAAGTATTA	84759
rs756294537	snp	A/C	1.64798e-05	0.00287047	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505606	CCGGAGATGGCGTAC[A/C]TCAGCTCTAACAGAA	84759
rs756371891	snp	A/C			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508855	AGTGAATTGAAGTGA[A/C]TATGCAGCAAGAAGT	84759
rs756526997	snp	A/G			intron-variant	PCGF1	GRCh38.p7	2:74507455	CGCAACCACGCAGGC[A/G]CACTGGGCACTCTGT	84759
rs756543141	snp	C/G/T	0.000143761	0.00847701	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507649	GCGATCGCAATCTGG[C/G/T]CCCCCTGAGGAGACG	84759
rs756676061	snp	C/G	3.29451e-05	0.00405851	missense, intron-variant	PCGF1	GRCh38.p7	2:74506026	GTGGTCAAAGCTGCT[C/G]AAGGGGAGGCCGAGG	84759
rs756885249	snp	G/T			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507860	TAATTAAGGAGTGGG[G/T]GGGGGGGAGCACAGG	84759
rs757463673	snp	A/C	1.65457e-05	0.00287621	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505506	CTCTGTCCCTCCTTT[A/C]TTAGCCCCTTCTCCC	84759
rs757625527	snp	C/T			intron-variant	PCGF1	GRCh38.p7	2:74506465	CGCCTGTAGTCCCAG[C/T]TACTCAGGAGGCTGA	84759
rs757645719	snp	C/T	3.95351e-05	0.00444589	intron-variant	PCGF1	GRCh38.p7	2:74507182	CACCAATCATCCACC[C/T]TCAAACCCCAACCCG	84759
rs757735782	snp	A/G	1.65102e-05	0.00287312	intron-variant	PCGF1	GRCh38.p7	2:74507007	TTGGTGAAGACTAGG[A/G]ACTGGAAGAACTAGG	84759
rs757854168	snp	A/G	1.64776e-05	0.00287028	intron-variant	PCGF1	GRCh38.p7	2:74505658	GAGCAGGGAGGGGAG[A/G]GAAGAGGGCAAGGTG	84759
rs757925313	snp	C/T			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509174	TACACTTCAAATATT[C/T]GCAGTTTATATGTCC	84759
rs757946627	in-del	-/CAAT	3.76361e-05	0.00433781	intron-variant	PCGF1	GRCh38.p7	2:74507170	TACACCCTCCGTCAC[-/CAAT]CATCCACCCTCAAAC	84759
rs758175845	snp	G/T	1.658e-05	0.00287919	intron-variant	PCGF1	GRCh38.p7	2:74506265	CACCTAGAAGAAGGT[G/T]AAGTATGAGAATAAA	84759
rs758352040	snp	A/G	4.94385e-05	0.0049716	intron-variant	PCGF1	GRCh38.p7	2:74506167	TCTTTACTGTCCCGC[A/G]GCCAAGGACATACCT	84759
rs758456401	snp	C/G	1.65075e-05	0.00287289	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505292	CTGTAGGATGGTTGG[C/G]GGGAGTCTGAAGGGG	84759
rs758463215	snp	A/G	2.6021e-05	0.00360691	synonymous-codon, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505345	CTGGCTTACCTTGCC[A/G]AACCAGCGGGAGAGC	84759
rs758536529	snp	C/T	0.000101836	0.00713497	intron-variant	PCGF1	GRCh38.p7	2:74506299	TTAGCCCTTCGGGGC[C/T]GGGCGCGGTGGCTCA	84759
rs758595881	snp	C/G			intron-variant	PCGF1	GRCh38.p7	2:74507169	ATACACCCTCCGTCA[C/G]CAATCATCCACCCTC	84759
rs758625790	in-del	-/C	1.65499e-05	0.00287657	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505232	TCAGTGGGGAATGTT[-/C]TTATATTATTCAAAG	84759
rs758685977	snp	A/C	1.65064e-05	0.00287279	intron-variant	PCGF1	GRCh38.p7	2:74506932	TCTGGAAACTGGATT[A/C]ATGGGCTGGGTGGGG	84759
rs759025777	snp	C/G	9.89364e-05	0.00703267	intron-variant	PCGF1	GRCh38.p7	2:74506698	TCAGCAATTAGTCCT[C/G]AAGAGGCCCCTCAAA	84759
rs759055592	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506859	CTTGCTAGTTTGGAG[A/G]TACTTCACAATACAA	84759
rs759438760	snp	A/C	3.29647e-05	0.00405971	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505589	CGGTGACACAGGACC[A/C]TCCGGAGATGGCGTA	84759
rs759575188	in-del	-/A			intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505319	GGGGTGTGATCCCAG[-/A]GGAGGGTGGCCTGGC	84759
rs759766765	snp	C/T	1.64776e-05	0.00287028	intron-variant	PCGF1	GRCh38.p7	2:74505948	CCCCTGACCTTCTCC[C/T]CACCTCAGCCGCTCC	84759
rs760137841	snp	C/T	5.28527e-05	0.00514039	upstream-variant-2KB, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505146	GGGGCTTGGCCCCTA[C/T]CTCCTCTTCTCTTTC	84759
rs760444516	snp	C/T	0.000109191	0.00738808	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505335	GGAGGGTGGCCTGGC[C/T]TACCTTGCCGAACCA	84759
rs760486687	snp	A/G	2.14968e-05	0.00327841	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505442	GGAGATGGGGGCATA[A/G]TTTTAGGAACTTTCT	84759
rs760532339	snp	C/G	1.69847e-05	0.00291411	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507137	TCTTTGATCTTCACT[C/G]GAACCTCCTCCTGAA	84759
rs760556202	snp	A/C			intron-variant	PCGF1	GRCh38.p7	2:74506958	TGGGGTGCCTGGATG[A/C]GTGAGGCAGGCCGCA	84759
rs760574287	snp	A/C	5.67843e-05	0.00532813	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507597	CCGTAGCGGGTCCAT[A/C]TTGTACACTGACTGG	84759
rs760642895	snp	A/C	1.64849e-05	0.00287092	intron-variant	PCGF1	GRCh38.p7	2:74505927	TGGCACTGTCACCTC[A/C]TGCAACCCCTGACCT	84759
rs761125987	snp	C/T			intron-variant	PCGF1	GRCh38.p7	2:74505825	CCTCCTCTTCCCCAC[C/T]CAGAGCCATGATATA	84759
rs761274678	snp	A/G	0.000170236	0.00922437	intron-variant	PCGF1	GRCh38.p7	2:74506300	TAGCCCTTCGGGGCC[A/G]GGCGCGGTGGCTCAC	84759
rs761354125	in-del	-/C	1.648e-05	0.0028705	intron-variant	PCGF1	GRCh38.p7	2:74507188	TCATCCACCCTCAAA[-/C]CCCAACCCGTGCGCC	84759
rs761381237	snp	A/G	1.64784e-05	0.00287035	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505424	AGGAGCTGCACCTAG[A/G]AGGGAGATGGGGGCA	84759
rs761481197	in-del	-/GGG	1.65999e-05	0.00288091	upstream-variant-2KB, cds-indel, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505130	GGAGTGGGATGGGGT[-/GGG]GGCTTGGCCCCTACC	84759
rs761559288	snp	A/T	6.60589e-05	0.00574675	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507106	GCATAGGCAGCAAAC[A/T]ATGTGTTCATTCAAG	84759
rs761938351	snp	G/T	6.17799e-05	0.00555753	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507632	GGTTCCGAAGCCTCA[G/T]CGCGATCGCAATCTG	84759
rs762018354	snp	A/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508534	GAGGTATTAACATCA[A/G]ATGCAACTGGAGATA	84759
rs762307435	snp	A/T			intron-variant	PCGF1	GRCh38.p7	2:74506362	GTGGGCAGATCATGA[A/T]GTCAGGAGATTGAGG	84759
rs762431094	snp	C/G	4.75703e-05	0.00487677	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505200	GGATGGCTAAGGAGA[C/G]AATGAGGAAGTAGTA	84759
rs762497561	snp	A/G	2.93302e-05	0.00382939	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505321	GGGTGTGATCCCAGG[A/G]AGGGTGGCCTGGCTT	84759
rs763001359	snp	C/G	1.64822e-05	0.00287068	intron-variant	PCGF1	GRCh38.p7	2:74505728	GGCCCTCCCCTCAGC[C/G]CTTCTCACCTGCAGG	84759
rs763085244	snp	G/T	5.73214e-05	0.00535326	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507610	ATCTTGTACACTGAC[G/T]GGAGCTGGTTCCGAA	84759
rs763229430	snp	C/T			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508429	TGTAGTAGCATAGGC[C/T]CAGTCCCGCACTTGG	84759
rs763622837	in-del	-/AAG	6.5912e-05	0.00574035	intron-variant	PCGF1	GRCh38.p7	2:74506134	AGAGCAAAACTGGGC[-/AAG]AAGAATGCTCTGGGG	84759
rs763782560	snp	A/G	0.000388614	0.013934	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505209	AGGAGAGAATGAGGA[A/G]GTAGTAGTCAGTGGG	84759
rs764144449	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504684	TATAATGCAATTCTT[C/T]GGATTTTTCTTTAAA	84759
rs764280100	snp	C/T			intron-variant	PCGF1	GRCh38.p7	2:74506305	CTTCGGGGCCGGGCG[C/T]GGTGGCTCACGCCTG	84759
rs764289134	snp	G/T	5.80568e-05	0.00538749	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507618	CACTGACTGGAGCTG[G/T]TTCCGAAGCCTCATC	84759
rs764380743	snp	C/T	1.91896e-05	0.00309749	intron-variant	PCGF1	GRCh38.p7	2:74507174	CCCTCCGTCACCAAT[C/T]ATCCACCCTCAAACC	84759
rs764464936	snp	C/T			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508440	AGGCCCAGTCCCGCA[C/T]TTGGGGACTACGCGG	84759
rs764543076	snp	A/T	1.64768e-05	0.00287021	intron-variant	PCGF1	GRCh38.p7	2:74506108	CACATTCCATACTCC[A/T]CTTTCCCCAGAGAGC	84759
rs764592260	snp	C/T	5.22234e-05	0.00510969	upstream-variant-2KB, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505149	GCTTGGCCCCTACCT[C/T]CTCTTCTCTTTCACA	84759
rs764663796	snp	A/T			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504552	GCAGTCCCCAAGTAC[A/T]TGCTGAATCCTGTAT	84759
rs764811331	in-del	-/TG	5.69039e-05	0.00533373	frameshift-variant, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507610	ATCTTGTACACTGAC[-/TG]GAGCTGGTTCCGAAG	84759
rs764861540	snp	A/G	1.65581e-05	0.00287728	intron-variant	PCGF1	GRCh38.p7	2:74506259	TCTCTTCACCTAGAA[A/G]AAGGTGAAGTATGAG	84759
rs764919639	snp	A/G	1.64876e-05	0.00287116	intron-variant	PCGF1	GRCh38.p7	2:74506701	GCAATTAGTCCTCAA[A/G]AGGCCCCTCAAAGTC	84759
rs765249786	snp	A/G	9.88745e-05	0.00703047	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505600	GACCCTCCGGAGATG[A/G]CGTACCTCAGCTCTA	84759
rs765514462	snp	G/T	1.6473e-05	0.00286988	missense, intron-variant	PCGF1	GRCh38.p7	2:74505972	CCGCTCCAGGCACAG[G/T]TTCAACTGCTCATCA	84759
rs765652918	in-del	-/C	5.4778e-05	0.00523316	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505140	GGGGTGGGGGCTTGG[-/C]CCCTACCTCCTCTTC	84759
rs766007115	snp	A/G	1.65064e-05	0.00287279	missense, intron-variant	PCGF1	GRCh38.p7	2:74506228	CCTCGGGACTGGTAG[A/G]ATTCCCGAATCCGTT	84759
rs766101868	snp	C/T	1.64789e-05	0.0028704	intron-variant	PCGF1	GRCh38.p7	2:74506156	ATGCTCTGGGGTCTT[C/T]ACTGTCCCGCGGCCA	84759
rs766118811	snp	G/T	4.26567e-05	0.00461806	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505449	GGGGCATAATTTTAG[G/T]AACTTTCTGGCAGGT	84759
rs766200561	snp	A/G	5.67489e-05	0.00532646	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507600	TAGCGGGTCCATCTT[A/G]TACACTGACTGGAGC	84759
rs766316107	snp	C/T	7.92759e-05	0.00629537	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505343	GCCTGGCTTACCTTG[C/T]CGAACCAGCGGGAGA	84759
rs766403843	snp	C/G	1.71938e-05	0.002932	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507142	GATCTTCACTCGAAC[C/G]TCCTCCTGAAGATAC	84759
rs766489461	snp	A/G	1.64879e-05	0.00287118	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505746	TCTCACCTGCAGGAC[A/G]CTTTTATTCTTGTCT	84759
rs766691973	snp	A/G	3.29582e-05	0.00405931	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505620	CCTCAGCTCTAACAG[A/G]ACATCGGACATACTT	84759
rs766800336	in-del	-/G	9.48362e-05	0.00688543	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505304	TGGGGGGAGTCTGAA[-/G]GGGGTGTGATCCCAG	84759
rs767234906	snp	G/T	2.82937e-05	0.00376113	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505328	ATCCCAGGGAGGGTG[G/T]CCTGGCTTACCTTGC	84759
rs767242284	snp	A/G	1.6601e-05	0.00288101	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507121	AATGTGTTCATTCAA[A/G]TCTTTGATCTTCACT	84759
rs767304604	snp	C/T			intron-variant	PCGF1	GRCh38.p7	2:74505856	CTCTCTTCAAGGGGA[C/T]AGGCACTCACTCACT	84759
rs767839542	snp	C/T	6.5675e-05	0.00573002	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507639	AAGCCTCATCGCGAT[C/T]GCAATCTGGCCCCCC	84759
rs767976649	snp	G/T	1.64787e-05	0.00287038	intron-variant	PCGF1	GRCh38.p7	2:74506147	GCAAGAAGAATGCTC[G/T]GGGGTCTTTACTGTC	84759
rs768049953	snp	A/G	3.30049e-05	0.00406219	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506224	CAAACCTCGGGACTG[A/G]TAGAATTCCCGAATC	84759
rs768085313	snp	A/G	2.91252e-05	0.00381599	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505323	GTGTGATCCCAGGGA[A/G]GGTGGCCTGGCTTAC	84759
rs768092235	snp	A/G			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508635	TTAGACTTGGGGGAG[A/G]GGGTGGAAGTGTGGT	84759
rs768154360	snp	A/T	1.64762e-05	0.00287016	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505415	TTGTCAAAAAGGAGC[A/T]GCACCTAGGAGGGAG	84759
rs768275719	snp	A/G	1.64895e-05	0.00287132	intron-variant	PCGF1	GRCh38.p7	2:74507036	GGCAGTCTCCAAGGC[A/G]CTCACAAGTATGAAG	84759
rs768365540	snp	C/T			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507779	ACCCTCTGTAAGGCC[C/T]CGCCCACGTCCCTTT	84759
rs768419502	in-del	-/C	1.80361e-05	0.00300295	intron-variant	PCGF1	GRCh38.p7	2:74507157	CTCCTCCTGAAGATA[-/C]ACCCTCCGTCACCAA	84759
rs768702845	snp	C/T	1.64871e-05	0.00287111	intron-variant	PCGF1	GRCh38.p7	2:74505920	GGGTCATTGGCACTG[C/T]CACCTCCTGCAACCC	84759
rs768837386	snp	C/T	1.64944e-05	0.00287175	missense, intron-variant	PCGF1	GRCh38.p7	2:74506216	ACCCGGTCCAAACCT[C/T]GGGACTGGTAGAATT	84759
rs768910340	snp	A/C	1.67576e-05	0.00289457	intron-variant	PCGF1	GRCh38.p7	2:74506286	TGAGAATAAAGTATT[A/C]GCCCTTCGGGGCCGG	84759
rs769217563	snp	A/C	3.29609e-05	0.00405948	intron-variant	PCGF1	GRCh38.p7	2:74506889	ACTCTTGCAGACTGC[A/C]GGAAAAGAAAAGCAG	84759
rs769282648	snp	C/T	1.64939e-05	0.0028717	intron-variant	PCGF1	GRCh38.p7	2:74507028	AAGAACTAGGCAGTC[C/T]CCAAGGCACTCACAA	84759
rs769301591	snp	A/G			intron-variant	PCGF1	GRCh38.p7	2:74506585	AAAAAAAGAAAAAAA[A/G]GAATAAAGTATTAGC	84759
rs769554039	snp	A/G			missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505575	GGTTTAGCATCAAGC[A/G]GTGACACAGGACCCT	84759
rs769745077	snp	A/G	1.64806e-05	0.00287054	intron-variant	PCGF1	GRCh38.p7	2:74505713	GAGTCTCCTTAGAGA[A/G]GCCCTCCCCTCAGCC	84759
rs769987039	snp	C/T	4.94295e-05	0.00497115	intron-variant	PCGF1	GRCh38.p7	2:74506093	AGGTGGCTGGTGGCA[C/T]ACATTCCATACTCCT	84759
rs770098587	snp	A/C	4.59485e-05	0.00479293	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505378	TATCTGCTTCATTGT[A/C]ATGTGATCAGGGAGA	84759
rs770323959	snp	C/G/T	2.47236e-05	0.00351586	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505316	GAAGGGGGTGTGATC[C/G/T]CAGGGAGGGTGGCCT	84759
rs770496010	snp	C/T	5.11854e-05	0.00505866	intron-variant	PCGF1	GRCh38.p7	2:74506303	CCCTTCGGGGCCGGG[C/T]GCGGTGGCTCACGCC	84759
rs770773390	snp	G/T			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508266	CCTGCTGCCGGGGAT[G/T]GGGGGGGCAGGCCCT	84759
rs770857013	snp	C/G	1.64754e-05	0.00287009	intron-variant	PCGF1	GRCh38.p7	2:74506066	GCTGGCTCTGAGAAA[C/G]ATAGGGTAGTGAGGT	84759
rs771368877	snp	A/G	3.11027e-05	0.0039434	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505308	GGGAGTCTGAAGGGG[A/G]TGTGATCCCAGGGAG	84759
rs771444379	snp	A/G	4.39416e-05	0.00468709	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505437	AGGAGGGAGATGGGG[A/G]CATAATTTTAGGAAC	84759
rs771462635	snp	G/T	5.57833e-05	0.00528096	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505134	TGGGATGGGGTGGGG[G/T]CTTGGCCCCTACCTC	84759
rs771546792	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506850	GGGGCAGTACTTGCT[A/G]GTTTGGAGGTACTTC	84759
rs771608876	snp	A/G	1.8897e-05	0.00307378	utr-variant-5-prime, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507679	GCCATCTTAAAGGCT[A/G]ATCCCAGCCGGCCAC	84759
rs771723259	in-del	-/AAT	4.98186e-05	0.00499067	intron-variant	PCGF1	GRCh38.p7	2:74506275	AAGGTGAAGTATGAG[-/AAT]AAAGTATTAGCCCTT	84759
rs771964188	snp	C/T			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508036	GTCGGTCTTCTGTGA[C/T]GACGACCCTGCTGAA	84759
rs772056238	snp	A/G	0.000148267	0.00860879	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506733	GGTTGGTGACTCACT[A/G]TCTTGCAAGCCAGGC	84759
rs772212789	snp	C/T	1.64852e-05	0.00287094	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505740	AGCCCTTCTCACCTG[C/T]AGGACGCTTTTATTC	84759
rs772333079	snp	A/G	1.66305e-05	0.00288357	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505118	GGGGAGGGAAGGGGA[A/G]TGGGATGGGGTGGGG	84759
rs772971646	snp	C/T			synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506754	CAAGCCAGGCACCAG[C/T]TTATACACGATGTCC	84759
rs773146929	snp	C/T	1.67312e-05	0.00289229	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507129	CATTCAAGTCTTTGA[C/T]CTTCACTCGAACCTC	84759
rs773230941	snp	A/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508085	TCTCCTCGTAATGCC[A/G]CCCTGTCGGCGTCCG	84759
rs773363549	snp	A/T	6.06116e-05	0.00550474	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505119	GGGAGGGAAGGGGAG[A/T]GGGATGGGGTGGGGG	84759
rs773857170	snp	A/G	2.21168e-05	0.00332534	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505423	AAGGAGCTGCACCTA[A/G]GAGGGAGATGGGGGC	84759
rs773898893	snp	C/G/T	6.60148e-05	0.0057449	missense, intron-variant	PCGF1	GRCh38.p7	2:74506225	AAACCTCGGGACTGG[C/G/T]AGAATTCCCGAATCC	84759
rs773947514	snp	A/C	7.58984e-05	0.00615983	intron-variant	PCGF1	GRCh38.p7	2:74507539	CCCCAATTCGCACCG[A/C]TGGCCGACCACAGCA	84759
rs774036209	snp	G/T	1.64923e-05	0.00287156	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507094	GAAGTAGCCGGCGCA[G/T]AGGCAGCAAACAATG	84759
rs774208250	snp	C/T			intron-variant	PCGF1	GRCh38.p7	2:74506664	GAGTCCTACCAAACC[C/T]GTCACCTCAAGCTGC	84759
rs774298527	snp	A/C/T	0.000462149	0.0151943	intron-variant	PCGF1	GRCh38.p7	2:74505782	AGAACTGGGGGGAAA[A/C/T]AGACACAGGTTAGGG	84759
rs774664717	snp	A/C	1.64779e-05	0.00287031	intron-variant	PCGF1	GRCh38.p7	2:74506138	CAAAACTGGGCAAGA[A/C]GAATGCTCTGGGGTC	84759
rs774774499	snp	A/G	4.94858e-05	0.00497398	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506218	CCGGTCCAAACCTCG[A/G]GACTGGTAGAATTCC	84759
rs774842757	snp	C/T			missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505587	AGCGGTGACACAGGA[C/T]CCTCCGGAGATGGCG	84759
rs774859081	snp	A/G	3.29815e-05	0.00406075	intron-variant	PCGF1	GRCh38.p7	2:74507031	AACTAGGCAGTCTCC[A/G]AGGCACTCACAAGTA	84759
rs775067082	snp	C/T	5.16382e-05	0.00508099	upstream-variant-2KB, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505152	TGGCCCCTACCTCCT[C/T]TTCTCTTTCACACTG	84759
rs775157136	snp	A/C	1.64811e-05	0.00287059	intron-variant	PCGF1	GRCh38.p7	2:74506892	CTTGCAGACTGCAGG[A/C]AAAGAAAAGCAGATT	84759
rs775335282	in-del	-/T	1.67033e-05	0.00288987	intron-variant	PCGF1	GRCh38.p7	2:74506283	TATGAGAATAAAGTA[-/T]TTAGCCCTTCGGGGC	84759
rs775429167	snp	C/G			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504613	CCTGTGGCCCCACTC[C/G]ATTTGTTTTTTAGAC	84759
rs775503579	snp	C/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508283	GGGGGGCAGGCCCTG[C/G]TTAATGATGATGATT	84759
rs775522434	snp	C/T	1.64817e-05	0.00287064	intron-variant	PCGF1	GRCh38.p7	2:74505727	AGGCCCTCCCCTCAG[C/T]CCTTCTCACCTGCAG	84759
rs775643368	snp	A/C	1.6486e-05	0.00287102	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506203	AGTGGGCTGGGTGAC[A/C]CGGTCCAAACCTCGG	84759
rs776197615	snp	A/G	1.7056e-05	0.00292022	intron-variant	PCGF1	GRCh38.p7	2:74506304	CCTTCGGGGCCGGGC[A/G]CGGTGGCTCACGCCT	84759
rs776470587	snp	C/T			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509510	TCTGGTTAGCACTTA[C/T]TAGCATTCTATCATT	84759
rs776578161	snp	G/T	2.10064e-05	0.0032408	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505455	TAATTTTAGGAACTT[G/T]CTGGCAGGTCAAAAA	84759
rs776667435	snp	A/C	1.64795e-05	0.00287045	intron-variant	PCGF1	GRCh38.p7	2:74505941	CCTGCAACCCCTGAC[A/C]TTCTCCTCACCTCAG	84759
rs776745704	snp	A/C	0.000229621	0.0107125	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507605	GGTCCATCTTGTACA[A/C]TGACTGGAGCTGGTT	84759
rs776776763	snp	C/T	8.23744e-05	0.0064172	intron-variant	PCGF1	GRCh38.p7	2:74506068	TGGCTCTGAGAAAGA[C/T]AGGGTAGTGAGGTGG	84759
rs777054064	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506858	ACTTGCTAGTTTGGA[A/G]GTACTTCACAATACA	84759
rs777234621	snp	C/T	3.31044e-05	0.0040683	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505142	GGTGGGGGCTTGGCC[C/T]CTACCTCCTCTTCTC	84759
rs777274458	snp	A/G	1.64773e-05	0.00287026	intron-variant	PCGF1	GRCh38.p7	2:74505661	CAGGGAGGGGAGGGA[A/G]GAGGGCAAGGTGTGT	84759
rs777513561	snp	A/G			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509182	AAATATTTGCAGTTT[A/G]TATGTCCATTATACT	84759
rs777526488	snp	C/T	9.86047e-05	0.00702087	utr-variant-5-prime, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507691	GCTGATCCCAGCCGG[C/T]CACTTCCGGTGCCGC	84759
rs778024081	snp	C/T	3.17748e-05	0.00398577	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505298	GATGGTTGGGGGGAG[C/T]CTGAAGGGGGTGTGA	84759
rs778284095	snp	G/T	8.23703e-05	0.00641704	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506828	CGTGGATCTTAATGT[G/T]GCACATGGGGCAGTA	84759
rs778403089	snp	A/G	1.77222e-05	0.0029767	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507667	CCCTGAGGAGACGCC[A/G]TCTTAAAGGCTGATC	84759
rs778579065	snp	A/T			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508983	ACTGTTTTCCTTGAG[A/T]CCCCCTTCGCCTGTT	84759
rs778657178	in-del	-/AGA	4.96413e-05	0.00498179	intron-variant	PCGF1	GRCh38.p7	2:74506255	CGTTTCTCTTCACCT[-/AGA]AGAAGGTGAAGTATG	84759
rs778673634	snp	A/G	1.64746e-05	0.00287002	missense, intron-variant	PCGF1	GRCh38.p7	2:74506051	CCGAGGTTGCTCAGT[A/G]CTGGCTCTGAGAAAG	84759
rs778855568	snp	A/C/G	3.03044e-05	0.00389247	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505315	TGAAGGGGGTGTGAT[A/C/G]CCAGGGAGGGTGGCC	84759
rs778875792	snp	C/T	1.65004e-05	0.00287227	intron-variant	PCGF1	GRCh38.p7	2:74506930	CCTCTGGAAACTGGA[C/T]TCATGGGCTGGGTGG	84759
rs779159419	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506787	CATGACCCGGTCCAG[C/T]TTGAGGTTGAGCAGT	84759
rs779360371	snp	A/T	0.00013182	0.00811742	intron-variant	PCGF1	GRCh38.p7	2:74505651	GTTCTGGGAGCAGGG[A/T]GGGGAGGGAAGAGGG	84759
rs779456067	snp	C/T	1.64917e-05	0.00287151	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505553	GTGGGACTACTCACA[C/T]GCTGAGGGTTTAGCA	84759
rs779790566	snp	C/T			intron-variant	PCGF1	GRCh38.p7	2:74506629	TTGTCCTTCCCTCAT[C/T]TTTGGCCTTCTGCCT	84759
rs779910967	snp	A/G	3.29478e-05	0.00405867	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506044	GGGGAGGCCGAGGTT[A/G]CTCAGTGCTGGCTCT	84759
rs780004550	snp	A/C	1.64882e-05	0.00287121	intron-variant	PCGF1	GRCh38.p7	2:74505916	CTCTGGGTCATTGGC[A/C]CTGTCACCTCCTGCA	84759
rs780113960	snp	A/G			intron-variant	PCGF1	GRCh38.p7	2:74506274	GAAGGTGAAGTATGA[A/G]AATAAAGTATTAGCC	84759
rs780574338	snp	C/G	0.000157752	0.00887981	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505395	TGTGATCAGGGAGAA[C/G]TTCATTGTCAAAAAG	84759
rs780770812	snp	A/G	1.6473e-05	0.00286988	missense, intron-variant	PCGF1	GRCh38.p7	2:74506030	TCAAAGCTGCTGAAG[A/G]GGAGGCCGAGGTTGC	84759
rs781164270	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506763	CACCAGCTTATACAC[A/G]ATGTCCTGCATGACC	84759
rs781192441	snp	A/G			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507966	AGCCTGCGAAAGACT[A/G]CCCCCTCCTACCCCC	84759
rs781428989	in-del	-/G	1.64796e-05	0.00287046	intron-variant	PCGF1	GRCh38.p7	2:74505709	AGGTGAGTCTCCTTA[-/G]AGAGGCCCTCCCCTC	84759
rs781626993	snp	C/T	6.92657e-05	0.00588456	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505374	GCCATATCTGCTTCA[C/T]TGTCATGTGATCAGG	84759
rs781685220	snp	C/T			intron-variant	PCGF1	GRCh38.p7	2:74506468	CTGTAGTCCCAGCTA[C/T]TCAGGAGGCTGAGGC	84759
rs781776278	snp	C/T			intron-variant	PCGF1	GRCh38.p7	2:74507383	TTTCCCAGGGGAGAC[C/T]ACACAACGTCGGCGA	84759
rs796258650	in-del	-/C			upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507856	CCGTAATTAAGGAGT[-/C]GGGGGGGGGGGAGCA	84759