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

PHF1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs4231	snp	C/G	0.0988009	0.199095	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416197	TAGGGAGAACTACCC[C/G]CTATCTCTCCAGGTA	5252
rs437874	snp	C/G	0.0607131	0.163311	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409707	ACACACACACACACA[C/G]AGATCTGGATCCGTC	5252
rs442745	snp	A/G	0.462438	0.131795	intron-variant	PHF1	GRCh38.p7	6:33414464	AAGCTGGGAGAAATG[A/G]AGAAAAATGGGGCCA	5252
rs452513	snp	C/T	0.16976	0.236773	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408938	agcactttgggaggc[C/T]gaggtgggtggatca	5252
rs761583	snp	C/T	0.0352966	0.128072	intron-variant	PHF1	GRCh38.p7	6:33413682	CCTTCCCCATAACTG[C/T]CCCAAACCCTAAACT	5252
rs1053683	snp	C/T	0	0	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416675	TCACAGAGTCAGTTT[C/T]TGACTCTATCACAGT	5252
rs1329704	snp	A/T			intron-variant	PHF1	GRCh38.p7	6:33412966	ATGGAAAGGGGTGGT[A/T]TAACCTTTGCAGGCA	5252
rs2235982	snp	C/T	0.0970103	0.197722	intron-variant	PHF1	GRCh38.p7	6:33413027	AGAGGTTAAGGGACT[C/T]GTCCGAGGTCATATG	5252
rs3106196	snp	G/T	0.0922461	0.193943	intron-variant	PHF1	GRCh38.p7	6:33415166	GAGCAGGGGGAACCC[G/T]ATGGAGCAAATGGTG	5252
rs3116713	snp	A/G	0.0922941	0.193982	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414511	GAGAACGTTCTTCCA[A/G]GCTCCTCTCTGCTCT	5252
rs4457156	snp	A/G	0.00764807	0.061364	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411441	GAGCCCCGAATTTGA[A/G]GGTGACCTGACATAA	5252
rs4470839	snp	C/G/T	3.29457e-05	0.00405854	missense, upstream-variant-2KB, utr-variant-3-prime	KIFC1, PHF1	GRCh38.p7	6:33409647	CCCCCTGCCCCCAGG[C/G/T]GAACCAGTGTGTTAT	5252
rs6934613	snp	A/T	0	0	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412387	GTGCTGGCCAGATGG[A/T]CTGATGGGCTGCTAT	5252
rs9282516	in-del	-/TGGGGCTAACAGCGAGTGGAGGGCGGGGC			upstream-variant-2KB, downstream-variant-500B	PHF1, KIFC1	GRCh38.p7	6:33410582	CGGGGAGGGCGGGGC[lengthTooLong]GCGCGAGGGAGGAGG	5252
rs10531042	in-del	-/TG	0.49995	0.00499176	intron-variant	PHF1	GRCh38.p7	6:33414640	ACCCACCTGGAAGAC[-/TG]TGACTGAAAAGGATT	5252
rs11543058	snp	A/G	0.00164701	0.0286495	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416765	TCGGCCACTTCGTAA[A/G]GGTGCACAGAACTAC	5252
rs34581314	in-del	-/G			frameshift-variant, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412520	AGGTGGACAGTGCTA[-/G]GGGAGGTGTGTCTGG	5252
rs34705269	in-del	-/A			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409761	GTGTGTGTCCCTATG[-/A]TCTATGTATCGGGTG	5252
rs35103775	in-del	-/C			frameshift-variant, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33414973	CCCTTCAGGGCAGGG[-/C]CCTGGGGGAGGGGTC	5252
rs35768190	snp	A/C	0.0140508	0.0826316	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414255	CAGGGTGGATGTGGC[A/C]CATCTTGTCCTGTAT	5252
rs35985571	in-del	-/G			splice-acceptor-variant, intron-variant	PHF1	GRCh38.p7	6:33413735	CTGTGTTCCCCCTCA[-/G]GTGGAACCTGAAAAT	5252
rs41267645	snp	C/T	0.00522586	0.050849	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412705	TCTCACAGCTGCCCT[C/T]CCTGGAGAGGAACTC	5252
rs41267647	snp	A/G	0.188196	0.24224	intron-variant	PHF1	GRCh38.p7	6:33414680	GCGTAAGGAGGAACC[A/G]TTTTTTACAGCACTG	5252
rs41267649	snp	C/T	0.0398229	0.135372	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416696	GACTCTGTGACCTGG[C/T]GCACCCACTGCAGGT	5252
rs57440415	in-del	-/GT			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409753	TGTGTGTGTGTGTGT[-/GT]CCCTATGTCTATGTA	5252
rs57991968	snp	C/T	0.127599	0.217986	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408811	TGTTGGGATTATAGG[C/T]GTGAGCCACCCAGCC	5252
rs58223929	in-del	-/GTGT			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409751	TGTGTGTGTGTGTGT[-/GTGT]CCCTATGTCTATGTA	5252
rs73416053	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411325	CGGGCTGGGCCGACA[C/G]AAGTCCCTTCTCGGA	5252
rs73416054	snp	A/G	0.0287627	0.116422	intron-variant	PHF1	GRCh38.p7	6:33413305	CACCAAGGTAAAGGC[A/G]CTTCCCTGTTACCCT	5252
rs73741833	snp	C/T	0.0162398	0.0886349	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410007	TCGTCTTTTCTCCCC[C/T]CTGCTATCACCGGTT	5252
rs73741834	snp	A/G	0.0040646	0.0448974	intron-variant	PHF1	GRCh38.p7	6:33414904	TATAGAGATGGGGAG[A/G]TCTTGGGGGTGTCCG	5252
rs76139322	snp	A/G	0.0490535	0.14873	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415743	CTCTTAGTCTCTAAC[A/G]CTGTTTCTCTGATTC	5252
rs76915106	snp	G/T			synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415107	GCCCGCTCCCTCTGC[G/T]CCTGGGGCTCGGGCT	5252
rs78862138	snp	A/G	0.0259427	0.110898	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415041	AGCCCCTGAGGAGGA[A/G]GCAGAAGGGGAAAGT	5252
rs111426477	snp	A/C/T	0	0	splice-donor-variant, intron-variant	PHF1	GRCh38.p7	6:33415146	AGAGGGCACTGCAGG[A/C/T]ACTGGAGCAGGGGGA	5252
rs111685107	snp	A/G/T	0	0	splice-donor-variant	PHF1	GRCh38.p7	6:33414111	CTACAGCTTCGCTGG[A/G/T]GAGCTGGATTGGGCA	5252
rs111693043	snp	A/C/G/T	0.0154538	0.0865337	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409745	TGTGTGTGTGTGTGT[A/C/G/T]TGTGTGTGTCCCTAT	5252
rs111979550	snp	C/T	0	0	intron-variant, upstream-variant-2KB, missense	KIFC1, PHF1	GRCh38.p7	6:33409496	GCAGAGGAGAACAAA[C/T]CATAACTGGCACCAG	5252
rs112250701	snp	A/G/T	0	0	intron-variant	PHF1	GRCh38.p7	6:33415147	TTCCCCCTGCTCCAG[A/G/T]ACCTGCAGTGCCCTC	5252
rs112889929	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410306	GCCTTTCCGTTCGAA[A/C]GGCTGGGGCTCTGCC	5252
rs112910184	snp	G/T			upstream-variant-2KB, downstream-variant-500B	PHF1, KIFC1	GRCh38.p7	6:33410570	GCGCGACTCGTCACG[G/T]GGAGGGCGGGGCGCG	5252
rs112930472	snp	C/G/T	0	0	intron-variant	PHF1	GRCh38.p7	6:33414112	TACAGCTTCGCTGGT[C/G/T]AGCTGGATTGGGCAT	5252
rs113107925	snp	C/T	0.097727	0.198275	intron-variant	PHF1	GRCh38.p7	6:33412965	CATGGAAAGGGGTGG[C/T]ATAACCTTTGCAGGC	5252
rs113133874	snp	C/T	0.0980852	0.198549	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412126	AAGATTGTGCCACTG[C/T]ACTCTGGCCTGGGCG	5252
rs113648187	snp	A/C/G/T	1.64735e-05	0.00286993	splice-donor-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416919	ATCTCAAAGTTCTCA[A/C/G/T]CGAACAAAATCTGTC	5252
rs113688166	snp	C/G	0	0	splice-donor-variant	PHF1	GRCh38.p7	6:33412590	AAGACATTAGCCCTG[C/G]TAAGACTCTAGAGAC	5252
rs113697385	snp	A/C	0	0	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411991	CATGGCCAACACCTC[A/C]TCTCTACTAAAAATA	5252
rs113984757	in-del	-/C	0.5	0	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416285	CTTCATGATTCCTGA[-/C]CCCCTCCCATCCTTC	5252
rs114197798	snp	A/G	0.000972738	0.0220323	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413249	CCTGGAGAGGGAGAG[A/G]GCACATCCTGGGTAT	5252
rs114485144	snp	C/T	0.0379877	0.132479	intron-variant	KIFC1	GRCh38.p7	6:33408659	ATTGAGTTGATATCC[C/T]AGCAGCTTCCAAAGG	5252
rs115894428	snp	C/G	0.0205511	0.0992634	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416284	TCCTTCATGATTCCT[C/G]ACCCCTCCCATCCTT	5252
rs116199362	snp	C/G	0.0502897	0.150386	intron-variant	PHF1	GRCh38.p7	6:33415178	CCCGATGGAGCAAAT[C/G]GTGGGGTGTGGGAAG	5252
rs137983869	in-del	-/AA	0.0379877	0.132479	intron-variant	PHF1	GRCh38.p7	6:33413126	TTAAATGAGATGGGT[-/AA]AGACTATTCCTGTCC	5252
rs138002129	snp	A/G/T	4.94453e-05	0.00497198	intron-variant	PHF1	GRCh38.p7	6:33414561	TGAGTTGGAGGGAAG[A/G/T]GGAGGCAAGGATGAG	5252
rs138236983	snp	A/G	0.00023354	0.0108035	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412289	CCCCCCGGCTGAGCC[A/G]CTCTGGTGCCTCCTC	5252
rs138332034	snp	C/G	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33413136	TGGGTAAAGACTATT[C/G]CTGTCCCAATACCAA	5252
rs138574267	snp	C/G	1.64991e-05	0.00287215	stop-gained, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416681	ATAGAGTCAGAAACT[C/G]ACTCTGTGACCTGGC	5252
rs138734488	snp	A/G	5.08281e-05	0.00504098	missense, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415870	AAGTGCCCCCCACTC[A/G]ATGACTGCCTCATCT	5252
rs139202558	snp	A/C	0.0241627	0.107227	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415378	TGCTCCCAATTATTC[A/C]CATCTTCTGGACTTT	5252
rs139787773	snp	C/G	1.65861e-05	0.00287972	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415127	AGGGAGCGGGCTCAT[C/G]TGCAGAGGGCACTGC	5252
rs140068887	snp	C/G	0.000115307	0.00759211	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416932	CACCGAACAAAATCT[C/G]TCAAAGCTGGGACCA	5252
rs140101976	snp	A/G	1.64999e-05	0.00287222	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413448	CCCTATGCCCGGGCC[A/G]TGCTGGGTATGAAGC	5252
rs140266539	snp	A/C	1.78867e-05	0.00299049	synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415096	AGTGCGCAATCAGCC[A/C]GAGCCCCAGGAGCAG	5252
rs140386895	snp	C/T	0.000153988	0.00877328	missense, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415593	CTCCAACCCCAGCAG[C/T]CCCATCCGGATGTTT	5252
rs141011458	snp	C/G	0.000115328	0.0075928	missense, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415650	CGCAGGGACCTCTGG[C/G]GACAGTGGACCCCCA	5252
rs141157797	snp	A/C/G	0.000548148	0.0165463	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415097	GTGCGCAATCAGCCC[A/C/G]AGCCCCAGGAGCAGA	5252
rs141218981	in-del	-/G	0.0528381	0.153711	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411705	ACTAGGTTTGGGGTC[-/G]GGGGGGAGGGCTGTT	5252
rs141323325	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410134	CTTGGTCACTAGTTA[C/T]AGGTAACTTTCACCC	5252
rs141510460	snp	A/G	6.65225e-05	0.00576687	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415950	CTTCTCCCCTGTGCC[A/G]TAGTTTGTCTCCTGG	5252
rs141684599	snp	C/G	0.00118538	0.0243163	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416953	GCTGGGACCAAGGAA[C/G]TTTGGGTTTTAATCA	5252
rs142622704	snp	A/T	0.00358779	0.0422022	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409867	GTTTGGTTTTTTTTT[A/T]AAATAAAGGTTTTAT	5252
rs142630097	snp	A/T	4.94303e-05	0.00497119	stop-gained, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415606	AGCCCCATCCGGATG[A/T]TTGCTTCCTTCCACC	5252
rs143261073	snp	A/G	0.000307953	0.0124049	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412422	GGGTACCATCAAAAA[A/G]GTAAGACCTTCTACC	5252
rs143277706	snp	C/T			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411995	GCCAACACCTCATCT[C/T]TACTAAAAATACAAA	5252
rs143366591	snp	A/G	0.00914312	0.0669923	intron-variant	PHF1	GRCh38.p7	6:33414165	ACAGTATTTCACTCT[A/G]TATGCCCCAACCTCC	5252
rs143414026	snp	C/T	0.000399281	0.0141238	intron-variant	KIFC1	GRCh38.p7	6:33408480	TGGATCTTTATTTCA[C/T]TAAGGGGTTTCTAAA	5252
rs144032908	snp	C/T	3.29451e-05	0.00405851	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414069	GAATGCTGTGTGTGT[C/T]GCGGGGGCCCTGAGA	5252
rs144092437	in-del	-/C	0.0252325	0.109451	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411429	CCCGGGGGCAGGGAG[-/C]CCCGAATTTGAGGGT	5252
rs144359180	snp	A/C/T	9.88735e-05	0.00703051	synonymous-codon, missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416737	CCCCTGTTCCACAGG[A/C/T]AATGCAATTACCTCG	5252
rs144660213	in-del	-/C			intron-variant	PHF1	GRCh38.p7	6:33413334	TTCCTGTGGGAGCCT[-/C]CCCATCCACAGCCTC	5252
rs144977635	snp	A/G	0.0260105	0.111035	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410197	GTTCCTTTGGTGGGT[A/G]TCGGCAAATGGGGAC	5252
rs145646205	snp	C/T	0.0232847	0.105357	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408984	GAGACCATCCTAACA[C/T]GGTGAAACCCCGTCT	5252
rs146564319	snp	A/C/T	0.00398691	0.0444912	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33409944	GAGCTGTGATCTGTA[A/C/T]CCTCTGCCAAACGTT	5252
rs146745688	snp	C/T	0.000642435	0.017911	intron-variant, synonymous-codon, nc-transcript-variant, missense, utr-variant-3-prime	PHF1	GRCh38.p7	6:33415288	TTACCAGGGCAGCAG[C/T]GGCTACAACTTCCGG	5252
rs146797571	snp	G/T	0.0209421	0.100162	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412070	GGGAGACTGAGGCAG[G/T]AGAATTGCCTGAACC	5252
rs147032936	snp	A/G	5.04316e-05	0.00502128	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33416022	GAGGGGACCCTGTCC[A/G]GGTCCTTGCTCGGAG	5252
rs147529537	snp	C/T	0.000480121	0.0154864	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413287	GTGTGTCTTTGCGAT[C/T]GCCACCAAGGTAAAG	5252
rs148447005	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409078	GGAGTCTGAGGCAGA[A/G]TGGCTTGAACCCGGG	5252
rs149582323	snp	C/T	0.000297015	0.0121827	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412344	TCCCACCTCTGGCCC[C/T]AGGCCTCGGCTTTGG	5252
rs149602053	snp	A/G	1.65119e-05	0.00287327	intron-variant	PHF1	GRCh38.p7	6:33413169	ACACACAGGTATGCA[A/G]TAAGTGGTCTACTAT	5252
rs149752386	snp	A/G	0.0232847	0.105357	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408980	GATCGAGACCATCCT[A/G]ACACGGTGAAACCCC	5252
rs149902794	snp	A/T	2.76308e-05	0.0037168	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415065	GGAAAGTGGAGGAGC[A/T]GGGGCCACCCTCAGC	5252
rs149930961	snp	C/T	9.99983e-05	0.0070703	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416613	GAAGGCGTTGAAGTA[C/T]CGCGGGGATCTTCAT	5252
rs150208032	snp	A/G	0.00086143	0.0207358	synonymous-codon, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415829	CCCCTGGAACTTCAC[A/G]TTGGTTTCCCCACAG	5252
rs150475632	snp	A/C	0.00478085	0.0486577	intron-variant	PHF1	GRCh38.p7	6:33413090	GATAATGCACCCCCT[A/C]ATCAAGACCATGGTC	5252
rs150662033	snp	C/T	0.000494087	0.0157099	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414330	TGAGATCCTCCCCTT[C/T]ACTTCTGAGAATTGG	5252
rs150787838	snp	C/T	0.00174477	0.0294846	intron-variant, synonymous-codon, nc-transcript-variant, missense, utr-variant-3-prime	PHF1	GRCh38.p7	6:33415267	ATCCCCCAGCCCTAA[C/T]CAGAGTTACCAGGGC	5252
rs150982256	snp	A/C/T	3.29518e-05	0.00405894	synonymous-codon, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415615	CGGATGTTTGCTTCC[A/C/T]TCCACCCTTCTGCCA	5252
rs180850031	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410322	GGCTGGGGCTCTGCC[C/T]GCTCGCTGCCCATTG	5252
rs181301885	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416861	GCAAGCCCTAGACTG[C/T]CCAGCAAGTCACACC	5252
rs181543604	snp	G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411711	GTTTGGGGTCGGGGG[G/T]AGGGCTGTTAGTTAC	5252
rs182280601	snp	C/G/T	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412086	AGAATTGCCTGAACC[C/G/T]GGGAGGTGGAGGTTG	5252
rs182453426	snp	C/T	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33413080	GTAAAATAAGGATAA[C/T]GCACCCCCTCATCAA	5252
rs182472476	snp	A/C			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409213	GATTGGTGCCAGTGT[A/C]CTTTAGACAGAACTC	5252
rs182515709	snp	A/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409566	AGGGCAGCCCTAGCA[A/T]TGGAGGATGGGAGAT	5252
rs182908431	snp	C/G	0.000399281	0.0141238	intron-variant	KIFC1	GRCh38.p7	6:33408647	TTGATTTTCAGTATT[C/G]AGTTGATATCCTAGC	5252
rs182983392	snp	C/T	4.96841e-05	0.00498393	synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33413820	GAGCAAGCCCCTCCT[C/T]TATGGGGACAGGTGA	5252
rs183773510	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416532	CATACATGACAAAAA[A/C]CAGGCAAAAGGCAGA	5252
rs184718345	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409814	GGTGCTTTATTGGGT[G/T]GAGGGCACCATGTCC	5252
rs185295374	snp	A/G			upstream-variant-2KB, downstream-variant-500B	PHF1, KIFC1	GRCh38.p7	6:33410615	GTGGTGGGGGCATCG[A/G]GAAGGGTGAATGGAG	5252
rs185500283	snp	C/T	0.00020026	0.0100045	intron-variant	PHF1	GRCh38.p7	6:33414714	CTATATCATTTCTCT[C/T]CTTGCCCCAGTTTCA	5252
rs185558876	snp	G/T	0.00676609	0.0577691	intron-variant	KIFC1	GRCh38.p7	6:33408447	CACCTAGTGATTTTA[G/T]CCAGCAGTGACCATA	5252
rs185611277	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33409962	TCTGCCAAACGTTTA[C/T]GTGGGAGGCGGGAGC	5252
rs185967149	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411786	CTGGTGATGGGTGCC[C/T]AGTGGTTTCCTATCA	5252
rs186209081	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408895	AGGAACCTCCTGGCC[A/G]GGCGCGGTGGCTCAT	5252
rs187143805	snp	A/G	0.000363168	0.0134704	intron-variant	PHF1	GRCh38.p7	6:33413168	CACACACAGGTATGC[A/G]ATAAGTGGTCTACTA	5252
rs187200502	snp	A/G			intron-variant	PHF1	GRCh38.p7	6:33412441	AGACCTTCTACCTCT[A/G]ACCTTCTTCCTAGTT	5252
rs187744360	snp	A/T	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409302	TTTCTAAGGAGTCCT[A/T]GTTCCTAAATGGGTG	5252
rs188454255	snp	A/G	0.00795532	0.062565	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416556	AGGCAGAGAGACCCA[A/G]AGACGGGATTTATTG	5252
rs188521783	snp	A/C/T	3.42173e-05	0.00413612	intron-variant	PHF1	GRCh38.p7	6:33413879	GATGCCCTCTTTCTT[A/C/T]GTGTTCCACCCTCAG	5252
rs188693894	snp	A/C			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411493	CTTAATGAGACGCGC[A/C]GGCCTGGGGAGACAG	5252
rs188810945	snp	C/T	0.000337479	0.0129856	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415762	TTTCTCTGATTCACA[C/T]GTGCTCTCCATTTCT	5252
rs189344915	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410108	TGCCCTCTAGCTATC[C/T]ACGCCCCCTCCTTGG	5252
rs190303475	snp	G/T	0.00358779	0.0422022	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409857	ATAAAGAATAGTTTG[G/T]TTTTTTTTTTAAATA	5252
rs190314289	snp	C/T	0.00398564	0.0444627	intron-variant	KIFC1	GRCh38.p7	6:33408525	ATCTTAGTTGTTCTG[C/T]ATTGGTTAGTCACGA	5252
rs190362846	snp	A/C/G/T	0.000198592	0.00996316	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413284	CCAGTGTGTCTTTGC[A/C/G/T]ATCGCCACCAAGGTA	5252
rs190884716	snp	A/G	0.000312971	0.0125055	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412555	GTTTGAGGATGATTC[A/G]CAGTTTCTGGTTCTA	5252
rs191235029	snp	C/T	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416266	AGGCCCTCTTCTCTA[C/T]CCTCCTTCATGATTC	5252
rs191656005	snp	A/G			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411947	GTGGGTGGATCATGA[A/G]GTCAGGAGTTCGAGA	5252
rs192120974	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409794	GGGTGGGAGGGTTGC[A/T]GGAGGGTGCTTTATT	5252
rs192420273	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409321	CCTAAATGGGTGTTA[C/T]TACTATTTTATCTCG	5252
rs192492638	snp	A/C	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409180	CAACAACAACAACAA[A/C]AAAAAGAGCCTCCTT	5252
rs192943959	snp	C/G	0.000798403	0.0199641	intron-variant	PHF1	GRCh38.p7	6:33414176	CTCTATATGCCCCAA[C/G]CTCCCACCTCAGGAC	5252
rs193286560	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409917	CAGATACTTTCATAT[C/T]TGTAAAAGTGGGAGC	5252
rs199696309	snp	A/G	8.24463e-05	0.00642	intron-variant	PHF1	GRCh38.p7	6:33414581	GCAAGGATGAGGCTC[A/G]GAAAGAGATGGAGAG	5252
rs199741480	snp	C/G	0.000164943	0.00907988	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416687	TCAGAAACTGACTCT[C/G]TGACCTGGCGCACCC	5252
rs199931674	in-del	-/GGGAGGGCGGGGCT			upstream-variant-2KB, downstream-variant-500B	PHF1, KIFC1	GRCh38.p7	6:33410569	GCGCGACTCGTCACG[-/GGGAGGGCGGGGCT]GGGAGGGCGGGGCGC	5252
rs200036660	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33412481	AATTCTGGTTCCCAT[C/T]TCATCCTGTTTGCTC	5252
rs200080102	snp	C/G	0.000614759	0.0175215	intron-variant	PHF1	GRCh38.p7	6:33414909	AGATGGGGAGGTCTT[C/G]GGGGTGTCCGGGAGG	5252
rs200107088	snp	A/G/T	0.00245531	0.0349636	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416795	CAAAATAGGTGGGTG[A/G/T]GGGAAGGGGATCACT	5252
rs200388150	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33414120	CGCTGGTGAGCTGGA[C/T]TGGGCATGACCTCAG	5252
rs200427336	snp	A/G	9.88728e-05	0.00703041	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416744	TCCACAGGCAATGCA[A/G]TTACCTCGGCCACTT	5252
rs200454650	snp	A/G	1.65474e-05	0.00287636	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416643	TGATGAGCAGGAACA[A/G]GGCTCATCATGGCAG	5252
rs200495976	snp	C/T	0.000100617	0.00709214	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415900	TTCCTCAGTTTCATC[C/T]CCATCCCCAGGTCTT	5252
rs200528141	snp	A/G	0.000713332	0.0188721	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415125	AGAGGGAGCGGGCTC[A/G]TCTGCAGAGGGCACT	5252
rs200696398	snp	A/G	0.000427705	0.0146174	intron-variant	PHF1	GRCh38.p7	6:33414848	ACTGGTCCAGGGGGG[A/G]TGGGGGAAATTCTCA	5252
rs200761761	snp	C/T	1.64806e-05	0.00287054	synonymous-codon, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416755	TGCAATTACCTCGGC[C/T]ACTTCGTAAGGGTGC	5252
rs200870071	snp	A/G	1.64749e-05	0.00287005	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414349	TCTGAGAATTGGGAC[A/G]GTTTGCTCCTGGGGG	5252
rs200906573	snp	C/T	0.00199806	0.0315443	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414342	CTTCACTTCTGAGAA[C/T]TGGGACAGTTTGCTC	5252
rs200951067	snp	C/T	3.34303e-05	0.00408828	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415118	CAGGAGCAGAGGGAG[C/T]GGGCTCATCTGCAGA	5252
rs201017824	snp	A/G	0.000280045	0.0118298	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409603	AAAAATGTTGTATTG[A/G]TTACGCTGCAAACTT	5252
rs201089147	snp	A/C/T	1.65119e-05	0.00287327	intron-variant	PHF1	GRCh38.p7	6:33413403	CCACCTGTCCTGTCT[A/C/T]TGCAGAGGGGAGGTG	5252
rs201145897	snp	A/G	0.00199792	0.0315431	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416666	CATGGCAGGACTGTG[A/G]TAGAGTCAGAAACTG	5252
rs201399798	snp	A/G			missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414340	CCCTTCACTTCTGAG[A/G]ATTGGGACAGTTTGC	5252
rs201507218	snp	C/G	0.00203008	0.031795	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414804	CCCCCTGTGGAGCCC[C/G]CTACTGGAGATGGAG	5252
rs201620118	snp	G/T	3.31972e-05	0.004074	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415995	TCCGAGGTGGGGTTG[G/T]TTACCTGTCCCGAGG	5252
rs201625667	snp	A/G	0.00199792	0.0315431	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412773	GGAACCGGCTGGTCA[A/G]CTGTGAGAAGTGTCG	5252
rs201684242	snp	A/G	4.94246e-05	0.0049709	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409599	TGGGAAAAATGTTGT[A/G]TTGGTTACGCTGCAA	5252
rs201717946	snp	A/G	0.000329413	0.0128296	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416921	CTCAAAGTTCTCACC[A/G]AACAAAATCTGTCAA	5252
rs201868307	snp	A/G	1.64789e-05	0.0028704	synonymous-codon, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416739	CCTGTTCCACAGGCA[A/G]TGCAATTACCTCGGC	5252
rs202000229	snp	A/G	0.000545224	0.016502	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415086	CACCCTCAGCAGTGC[A/G]CAATCAGCCCGAGCC	5252
rs202023663	snp	A/G	3.29957e-05	0.00406162	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415716	CTCTTCTTCCCCTCT[A/G]TGTGCTCAAGGCTCT	5252
rs202064015	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409594	GATCTTGGGAAAAAT[A/G]TTGTATTGGTTACGC	5252
rs202135073	snp	A/G			missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414319	GATTTTGATCGTGAG[A/G]TCCTCCCCTTCACTT	5252
rs202209041	snp	C/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412723	TGGAGAGGAACTCCT[C/G]TGTTGTGTCTGTCGC	5252
rs367602599	snp	A/G	0.000102731	0.00716623	intron-variant	PHF1	GRCh38.p7	6:33413880	ATGCCCTCTTTCTTC[A/G]TGTTCCACCCTCAGT	5252
rs367705535	snp	A/G/T	3.31023e-05	0.0040682	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412728	AGGAACTCCTCTGTT[A/G/T]TGTCTGTCGCTCTGA	5252
rs368152866	snp	C/T	3.36547e-05	0.00410198	intron-variant	PHF1	GRCh38.p7	6:33413689	GGTTTGGGACAGTTA[C/T]GGGGAAGGGGGTTTC	5252
rs368222331	snp	C/T	0.000217837	0.0104341	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415085	CCACCCTCAGCAGTG[C/T]GCAATCAGCCCGAGC	5252
rs368297880	snp	C/T	3.31395e-05	0.00407046	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412304	GCTCTGGTGCCTCCT[C/T]ACTTTGGGACCCAGC	5252
rs368520939	snp	A/C	0.000197044	0.00992388	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415040	GAGCCCCTGAGGAGG[A/C]GGCAGAAGGGGAAAG	5252
rs368818327	snp	C/G	1.6607e-05	0.00288153	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412295	GGCTGAGCCGCTCTG[C/G]TGCCTCCTCACTTTG	5252
rs368864667	snp	C/T	3.33673e-05	0.00408442	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415922	CCAGGTCTTCCTAGA[C/T]GCTCAGCACCCCCTT	5252
rs368875361	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33413956	CGTTACCTCACCTGT[C/T]TGCCCCGTCCTTGCT	5252
rs369171648	snp	C/T	0.000153988	0.00877328	intron-variant	PHF1	GRCh38.p7	6:33413315	AAGGCACTTCCCTGT[C/T]ACCCTTCCTGTGGGA	5252
rs369334642	snp	A/G	1.65149e-05	0.00287353	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415547	GGGGGAGAAGGTCCT[A/G]TTCCCCTGCTTCAGG	5252
rs369341035	snp	C/G	1.81979e-05	0.00301639	downstream-variant-500B, utr-variant-3-prime, missense, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416092	GGGAGGAGGGGGCAT[C/G]TTCTGAACAGCCTGC	5252
rs369369338	snp	C/T	1.6477e-05	0.00287024	intron-variant	PHF1	GRCh38.p7	6:33414378	GGAGGTAAGGGGTAG[C/T]GCAGTTTTGGGGGTT	5252
rs369609725	snp	C/T	0.0001812	0.00951667	intron-variant	PHF1	GRCh38.p7	6:33414022	GTAAGTGTGTTTGCT[C/T]CCTCTTGCCCATGTC	5252
rs369871473	snp	C/G	3.33517e-05	0.00408347	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33416009	GGTTACCTGTCCCGA[C/G]GGGACCCTGTCCGGG	5252
rs369954221	snp	A/G	1.64779e-05	0.00287031	intron-variant, missense, nc-transcript-variant, synonymous-codon, utr-variant-3-prime	PHF1	GRCh38.p7	6:33415289	TACCAGGGCAGCAGC[A/G]GCTACAACTTCCGGC	5252
rs369988459	snp	A/G	1.66123e-05	0.00288199	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412764	TGGTCCCTGGGAACC[A/G]GCTGGTCAGCTGTGA	5252
rs370122087	snp	C/T	1.66524e-05	0.00288547	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416616	GGCGTTGAAGTATCG[C/T]GGGGATCTTCATGAT	5252
rs370122217	snp	A/T	0.000230597	0.0107352	synonymous-codon, upstream-variant-2KB, utr-variant-3-prime	KIFC1, PHF1	GRCh38.p7	6:33409660	GGTGAACCAGTGTGT[A/T]ATTGGTACTGCTCAG	5252
rs370305108	snp	A/C/T	4.98238e-05	0.00499098	intron-variant	PHF1	GRCh38.p7	6:33413311	GGTAAAGGCACTTCC[A/C/T]TGTTACCCTTCCTGT	5252
rs370596406	snp	A/G	0.000101017	0.00710621	intron-variant	PHF1	GRCh38.p7	6:33413685	TTAGGGTTTGGGACA[A/G]TTATGGGGAAGGGGG	5252
rs370865709	snp	A/G	5.13809e-05	0.00506831	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412231	AACCTTCTCCTCCCC[A/G]TTTCTTTTCTGGCTA	5252
rs370882136	snp	A/G	0.00119737	0.0244387	intron-variant	PHF1	GRCh38.p7	6:33414167	AGTATTTCACTCTAT[A/G]TGCCCCAACCTCCCA	5252
rs370966068	snp	A/G	0.000636083	0.0178224	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415357	CTGCCCCTCCCCCAC[A/G]AAATATGCTCCCAAT	5252
rs370994570	snp	A/C	0.000153988	0.00877328	intron-variant	PHF1	GRCh38.p7	6:33414587	ATGAGGCTCGGAAAG[A/C]GATGGAGAGTGGAAG	5252
rs371083164	snp	C/T	0.000153988	0.00877328	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416667	ATGGCAGGACTGTGA[C/T]AGAGTCAGAAACTGA	5252
rs371196414	snp	C/T	3.31653e-05	0.00407204	intron-variant	PHF1	GRCh38.p7	6:33413596	CTGTGGAATGAATGA[C/T]GTGGTGGTGGATCCC	5252
rs371271580	snp	C/G/T	4.96597e-05	0.00498275	synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412729	GGAACTCCTCTGTTG[C/G/T]GTCTGTCGCTCTGAG	5252
rs371283742	snp	C/G/T	0.000102441	0.00715626	intron-variant	PHF1	GRCh38.p7	6:33414843	AGGTCACTGGTCCAG[C/G/T]GGGGATGGGGGAAAT	5252
rs371426764	snp	A/C/G	0.000103415	0.00719013	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415833	TGGAACTTCACATTG[A/C/G]TTTCCCCACAGACAT	5252
rs371490134	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412298	TGAGCCGCTCTGGTG[C/T]CTCCTCACTTTGGGA	5252
rs371672794	snp	C/T	3.30786e-05	0.00406672	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412315	TCCTCACTTTGGGAC[C/T]CAGCTTCTCCTGCTC	5252
rs371701025	snp	C/G/T	4.94485e-05	0.00497214	synonymous-codon, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416713	CACCCACTGCAGGTA[C/G/T]GGAAAGTTCCCCTGT	5252
rs371746919	snp	G/T			intron-variant	PHF1	GRCh38.p7	6:33414888	TCCTGGGGGGTATAT[G/T]TATAGAGATGGGGAG	5252
rs371767533	snp	A/T	1.65795e-05	0.00287914	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415128	GGGAGCGGGCTCATC[A/T]GCAGAGGGCACTGCA	5252
rs372034637	snp	C/T	6.62186e-05	0.00575369	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33413761	AAAATGCTGCAGTGC[C/T]GGAGCTGCCTGCAGT	5252
rs372508939	snp	A/T	1.6473e-05	0.00286988	intron-variant	PHF1	GRCh38.p7	6:33412445	CTTCTACCTCTGACC[A/T]TCTTCCTAGTTCCCT	5252
rs372535149	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414050	GTCCAGGTTCTATGA[A/G]TTTGAATGCTGTGTG	5252
rs372638583	snp	A/C	1.64749e-05	0.00287005	intron-variant	PHF1	GRCh38.p7	6:33415208	GGAGTCAAGGATTAT[A/C]TCTCAGTCCTTTGCC	5252
rs372667204	snp	A/C/G	0.000183518	0.00957752	intron-variant	PHF1	GRCh38.p7	6:33414719	TCATTTCTCTTCTTG[A/C/G]CCCAGTTTCATTTCA	5252
rs372713329	snp	C/T	4.95888e-05	0.00497915	intron-variant	PHF1	GRCh38.p7	6:33413391	CTCTGAAGCCACCCA[C/T]CTGTCCTGTCTCTGC	5252
rs372735655	snp	C/T	4.9831e-05	0.00499129	intron-variant	PHF1	GRCh38.p7	6:33413309	AAGGTAAAGGCACTT[C/T]CCTGTTACCCTTCCT	5252
rs372745281	snp	A/G	6.60589e-05	0.00574675	intron-variant	PHF1	GRCh38.p7	6:33413154	GTCCCAATACCAAGC[A/G]CACACAGGTATGCAA	5252
rs372895249	snp	C/T	6.60797e-05	0.00574765	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415544	CCAGGGGGAGAAGGT[C/T]CTGTTCCCCTGCTTC	5252
rs372962845	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409759	TGTGTGTGTGTCCCT[A/G]TGTCTATGTATCGGG	5252
rs373132487	snp	C/T	3.31433e-05	0.0040707	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413293	CTTTGCGATCGCCAC[C/T]AAGGTAAAGGCACTT	5252
rs373264072	snp	C/T	1.67433e-05	0.00289333	intron-variant	PHF1	GRCh38.p7	6:33414679	GGCGTAAGGAGGAAC[C/T]GTTTTTTACAGCACT	5252
rs373304211	snp	C/G	0.000153988	0.00877328	intron-variant	PHF1	GRCh38.p7	6:33414395	CAGTTTTGGGGGTTG[C/G]GATGGGACAGGGAGA	5252
rs373333588	snp	A/G	4.95405e-05	0.00497673	intron-variant, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415317	GGCCCACAGATGCCC[A/G]CTGCCTGCCCAGGTC	5252
rs373439668	snp	C/G/T	3.2948e-05	0.00405871	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414491	GCTTTCAGACACCCC[C/G/T]AAAGGAGAACGTTCT	5252
rs373454319	snp	G/T	1.6641e-05	0.00288448	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415946	CCCCCTTCTCCCCTG[G/T]GCCGTAGTTTGTCTC	5252
rs373555262	snp	C/G	3.69658e-05	0.00429902	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416120	TGCCTCTGCCCAGCT[C/G]CCCATTCACACACAC	5252
rs373575912	snp	A/C/G	4.94257e-05	0.004971	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409597	CTTGGGAAAAATGTT[A/C/G]TATTGGTTACGCTGC	5252
rs373582363	snp	C/T			intron-variant	KIFC1	GRCh38.p7	6:33408621	AAACAAGATAAATGC[C/T]GAATTATTTATTGAT	5252
rs373763326	snp	A/G	1.7184e-05	0.00293117	downstream-variant-500B, utr-variant-3-prime, missense, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416043	TTGCTCGGAGAGTAC[A/G]GCCTGATGGCTCTGT	5252
rs373787649	snp	C/G	0.000102272	0.00715022	intron-variant	PHF1	GRCh38.p7	6:33413876	AAGGATGCCCTCTTT[C/G]TTCGTGTTCCACCCT	5252
rs373928514	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412516	ATTCCAGGTGGACAG[C/T]GCTAGGGAGGTGTGT	5252
rs374034271	snp	A/T	0.000151532	0.00870304	intron-variant	PHF1	GRCh38.p7	6:33413688	GGGTTTGGGACAGTT[A/T]TGGGGAAGGGGGTTT	5252
rs374329100	snp	C/G	5.11854e-05	0.00505866	missense, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415861	CATCCCTAAAAGTGC[C/G]CCCCACTCGATGACT	5252
rs374352027	snp	G/T	0.000153988	0.00877328	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412300	AGCCGCTCTGGTGCC[G/T]CCTCACTTTGGGACC	5252
rs374614248	snp	A/C/T	4.9626e-05	0.00498106	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416646	TGAGCAGGAACAGGG[A/C/T]TCATCATGGCAGGAC	5252
rs374690890	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33413332	CCCTTCCTGTGGGAG[C/T]CTCCCATCCACAGCC	5252
rs374732683	snp	C/T	0.000329435	0.01283	intron-variant, synonymous-codon, missense	PHF1	GRCh38.p7	6:33415223	CTCTCAGTCCTTTGC[C/T]CCCTCTTCTAGGCCT	5252
rs374800838	snp	A/G			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409037	ACCGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCTC	5252
rs375193176	in-del	-/TG			intron-variant	PHF1	GRCh38.p7	6:33414642	CCACCTGGAAGACTG[-/TG]ACTGAAAAGGATTGA	5252
rs375282900	snp	A/G/T	6.59841e-05	0.00574355	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416684	GAGTCAGAAACTGAC[A/G/T]CTGTGACCTGGCGCA	5252
rs375421810	snp	A/G	0.000397977	0.0141007	intron-variant	PHF1	GRCh38.p7	6:33413597	TGTGGAATGAATGAT[A/G]TGGTGGTGGATCCCA	5252
rs375556383	snp	C/T	1.6473e-05	0.00286988	missense, upstream-variant-2KB, utr-variant-3-prime	KIFC1, PHF1	GRCh38.p7	6:33409662	TGAACCAGTGTGTTA[C/T]TGGTACTGCTCAGGC	5252
rs375821683	snp	C/T	0.000116257	0.00762331	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412763	GTGGTCCCTGGGAAC[C/T]GGCTGGTCAGCTGTG	5252
rs375893284	snp	A/C/T	0.000268685	0.0115875	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415010	CCCCTGGGGAAGCGC[A/C/T]GGAGGCCGGAGCCAG	5252
rs376222652	snp	A/G	1.64814e-05	0.00287061	intron-variant	PHF1	GRCh38.p7	6:33414430	GCGGAAAGGGGAAGA[A/G]AAGAAATCACTGCTC	5252
rs376261767	snp	A/C/G	3.31841e-05	0.00407323	intron-variant	PHF1	GRCh38.p7	6:33413602	AATGAATGATGTGGT[A/C/G]GTGGATCCCAGGAAA	5252
rs376342940	snp	A/G	0.000445122	0.0149118	intron-variant	PHF1	GRCh38.p7	6:33414585	GGATGAGGCTCGGAA[A/G]GAGATGGAGAGTGGA	5252
rs376639282	snp	A/G	6.66445e-05	0.00577216	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33416007	TTGGTTACCTGTCCC[A/G]AGGGGACCCTGTCCG	5252
rs376690709	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410213	TCGGCAAATGGGGAC[C/T]GGACCCCAGAGTCCA	5252
rs376699088	snp	A/G	0.000307953	0.0124049	downstream-variant-500B, utr-variant-3-prime, missense, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416087	GAGTGGGGAGGAGGG[A/G]GCATCTTCTGAACAG	5252
rs376794147	snp	C/T	6.8099e-05	0.0058348	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415350	TGCTCCTCTGCCCCT[C/T]CCCCACAAAATATGC	5252
rs376926102	snp	C/G/T	8.26322e-05	0.00642729	intron-variant	PHF1	GRCh38.p7	6:33413392	TCTGAAGCCACCCAC[C/G/T]TGTCCTGTCTCTGCA	5252
rs376998628	snp	C/T			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412262	GGCCCCCCCAGGATG[C/T]AATGGCGCAGCCCCC	5252
rs377029456	snp	C/T	6.58903e-05	0.00573941	intron-variant	PHF1	GRCh38.p7	6:33412446	TTCTACCTCTGACCT[C/T]CTTCCTAGTTCCCTT	5252
rs377077515	snp	C/T	0.000181191	0.00951644	intron-variant	PHF1	GRCh38.p7	6:33414141	ATGACCTCAGTGTAA[C/T]TCCACACCACAGTAT	5252
rs377134498	snp	A/C	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	PHF1	GRCh38.p7	6:33414780	TTTGGTCTCCATGCT[A/C]GGATGCCTCCCCCTG	5252
rs377166111	snp	C/T	4.94271e-05	0.00497102	intron-variant	PHF1	GRCh38.p7	6:33414003	GATGGCACAGTTTTC[C/T]TGTGTAAGTGTGTTT	5252
rs377170601	in-del	-/AA			intron-variant	PHF1	GRCh38.p7	6:33413127	TAAATGAGATGGGTA[-/AA]GACTATTCCTGTCCC	5252
rs377242808	snp	A/G	4.94694e-05	0.00497316	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415700	TCTATTACCAGTGAT[A/G]CTCTTCTTCCCCTCT	5252
rs377274632	snp	C/G	8.50347e-05	0.00651998	synonymous-codon, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415865	CCTAAAAGTGCCCCC[C/G]ACTCGATGACTGCCT	5252
rs377433705	snp	C/T	0.000494144	0.0157108	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409607	ATGTTGTATTGGTTA[C/T]GCTGCAAACTTTTAT	5252
rs377559003	snp	C/T	1.65392e-05	0.00287564	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416647	GAGCAGGAACAGGGC[C/T]CATCATGGCAGGACT	5252
rs377652391	snp	A/T			intron-variant	PHF1	GRCh38.p7	6:33412694	ACACTGTGTTCTCTC[A/T]CAGCTGCCCTCCCTG	5252
rs527265258	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412119	GTGAGCCAAGATTGT[A/G]CCACTGCACTCTGGC	5252
rs527370030	snp	A/G	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33412945	TCAGCCCAGGGAGAA[A/G]CAGCCATGGAAAGGG	5252
rs528176353	in-del	-/T	0.000362343	0.0134551	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409636	TCCTGTCTAACCCCC[-/T]TGCCCCCAGGTGAAC	5252
rs528546642	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416124	TCTGCCCAGCTCCCC[A/G]TTCACACACACCGGC	5252
rs528618368	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408901	CTCCTGGCCGGGCGC[A/G]GTGGCTCATGCCTGT	5252
rs529041898	snp	C/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410281	TTTCCTCCCGTCCCG[C/G]CCTTTCCCTGCCTTT	5252
rs529162448	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411873	TAGGCAAAGAAAATG[C/G]GGAGGCTGGCCGGGC	5252
rs529258636	snp	C/T			missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416750	GGCAATGCAATTACC[C/T]CGGCCACTTCGTAAG	5252
rs529323934	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408939	GCACTTTGGGAGGCT[A/G]AGGTGGGTGGATCAC	5252
rs529843371	snp	C/G			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412200	AAGAAAATGGGGAAG[C/G]TTTCTCAGCATTCAT	5252
rs530003205	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416182	CCTACAGCTGGGATG[C/T]ACCTGGAGAGATAGG	5252
rs530288059	snp	A/G	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33414602	AGATGGAGAGTGGAA[A/G]CCTGGAAGGGGAGGG	5252
rs530537499	snp	C/T	0.000148269	0.00860886	missense, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415635	CCCTTCTGCCAGCAC[C/T]GCAGGGACCTCTGGG	5252
rs530839734	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408991	TCCTAACACGGTGAA[A/T]CCCCGTCTCTACTAA	5252
rs531039830	snp	A/G	1.64749e-05	0.00287005	intron-variant	PHF1	GRCh38.p7	6:33415202	TGGGAAGGAGTCAAG[A/G]ATTATCTCTCAGTCC	5252
rs531913712	snp	C/T	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33413021	TCTAACCATATGACC[C/T]CGGACAAGTCCCTTA	5252
rs532869059	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412052	CTGTAATCCCACCTA[C/T]TTGGGAGACTGAGGC	5252
rs534233188	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant, intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411103	GCCTGGGGACCCCCC[A/G]GCCTCCGCCTGCACG	5252
rs534717202	snp	A/G	0.000399281	0.0141238	intron-variant	KIFC1	GRCh38.p7	6:33408593	TTTCTCTGAAATTCA[A/G]TTCATACAGGAAAAA	5252
rs534783081	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409142	CTGCACTCCAGCCTG[A/G]GCGACAGAGCAAGAC	5252
rs535538280	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409765	TGTGTCCCTATGTCT[A/G]TGTATCGGGTGAGGG	5252
rs536147182	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415451	TCTTGGCCTAGACCG[A/T]CTTCTAGAACTAGTG	5252
rs536163351	snp	C/T	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416360	TTAAAATTATTTAAC[C/T]CCTGGGGGCAGAGAC	5252
rs536733096	snp	C/T	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33413137	GGGTAAAGACTATTC[C/T]TGTCCCAATACCAAG	5252
rs537124666	in-del	-/A			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416437	TAAAGAGAAATAAAC[-/A]AATCTAGCAGCTCTG	5252
rs537481871	snp	A/G	0.00199481	0.0315187	intron-variant	PHF1	GRCh38.p7	6:33413931	TCCAGTCTCTTCCCA[A/G]CCTCTGCAGCGTTAC	5252
rs538085022	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411603	CTCTAAACTGAGTAG[C/G]CTTTGCTTCTACAAC	5252
rs538523324	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412170	CCATCTCAGGAAAAA[A/G]AAAAAAAAAAGAAAA	5252
rs539143860	snp	C/T	5.13747e-05	0.00506801	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412237	CTCCTCCCCATTTCT[C/T]TTCTGGCTAGGCCCC	5252
rs539204975	snp	C/G	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33413086	TAAGGATAATGCACC[C/G]CCTCATCAAGACCAT	5252
rs539502052	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	PHF1, KIFC1	GRCh38.p7	6:33410460	ACTCCCTCGCGCCAA[C/G]CGCCGACGGCCGCCG	5252
rs540282025	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416603	CTGGAAGTCAGAAGG[C/T]GTTGAAGTATCGCGG	5252
rs540342890	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408937	CAGCACTTTGGGAGG[C/T]TGAGGTGGGTGGATC	5252
rs540797551	snp	A/G			utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416547	ACAGGCAAAAGGCAG[A/G]GAGACCCAAAGACGG	5252
rs540936238	snp	C/T	0.000132203	0.00812921	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416811	GGGAAGGGGATCACT[C/T]AAAGATTTACCCAAA	5252
rs540960899	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409908	CCAAGAAGGCAGATA[C/T]TTTCATATCTGTAAA	5252
rs541063428	snp	A/C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415750	TCTCTAACACTGTTT[A/C/T]TCTGATTCACATGTG	5252
rs542734689	snp	A/C			upstream-variant-2KB, downstream-variant-500B	PHF1, KIFC1	GRCh38.p7	6:33410459	GACTCCCTCGCGCCA[A/C]CCGCCGACGGCCGCC	5252
rs543070138	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412416	ATACTTGGGTACCAT[C/T]AAAAAGGTAAGACCT	5252
rs543262022	snp	C/T			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409125	GAGCCGAGATCGCGC[C/T]ACTGCACTCCAGCCT	5252
rs544108878	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411980	AGTTTGGCCAACATG[A/G]CCAACACCTCATCTC	5252
rs545454270	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410012	TTTTCTCCCCTCTGC[C/T]ATCACCGGTTCTGGA	5252
rs545513651	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411725	GGAGGGCTGTTAGTT[A/T]CCGAGAGGAGAGCCA	5252
rs545536336	in-del	-/C	5.14201e-05	0.00507024	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412248	TCTTTTCTGGCTAGG[-/C]CCCCCCCAGGATGCA	5252
rs546018857	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416498	GACTAGAAGCACTTA[C/T]ATTCTCCCAACAAAT	5252
rs546629516	snp	A/C/T	3.72192e-05	0.00431375	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416145	ACACACCGGCACTTT[A/C/T]ATACCCTGACCTCTG	5252
rs546856171	snp	C/G	0.00438332	0.0466095	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409753	TGTGTGTGTGTGTGT[C/G]TCCCTATGTCTATGT	5252
rs547222452	snp	A/G			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412087	GAATTGCCTGAACCC[A/G]GGAGGTGGAGGTTGC	5252
rs547765970	snp	G/T	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416194	ATGTACCTGGAGAGA[G/T]AGGGGGTAGTTCTCC	5252
rs548143483	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416191	GGGATGTACCTGGAG[A/T]GATAGGGGGTAGTTC	5252
rs548194332	snp	G/T			intron-variant	KIFC1	GRCh38.p7	6:33408673	CTAGCAGCTTCCAAA[G/T]GTGACCAATGAATGT	5252
rs548207780	snp	A/G	0.000399281	0.0141238	intron-variant	KIFC1	GRCh38.p7	6:33408499	GGGGTTTCTAAATGG[A/G]GATTTTTCTAATCTT	5252
rs548473658	snp	A/G	0.000798403	0.0199641	intron-variant	PHF1	GRCh38.p7	6:33414667	GGATTGAGGAATGGC[A/G]TAAGGAGGAACCGTT	5252
rs550226747	snp	G/T	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33413600	GGAATGAATGATGTG[G/T]TGGTGGATCCCAGGA	5252
rs550517254	snp	A/G/T	1.65149e-05	0.00287353	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413489	ATATGGACTGAAGGG[A/G/T]CTGGACTGGGATGCT	5252
rs551010707	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	PHF1, KIFC1	GRCh38.p7	6:33410545	CGTGCGCAAAAGGGC[A/G]GTGGGTGGGGCGCGA	5252
rs552146910	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408995	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	5252
rs552385077	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416264	AGAGGCCCTCTTCTC[C/T]ACCCTCCTTCATGAT	5252
rs552938887	snp	C/G	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416291	TGATTCCTGACCCCT[C/G]CCATCCTTCCCATTT	5252
rs553070869	snp	A/G	0.000399281	0.0141238	intron-variant	KIFC1	GRCh38.p7	6:33408603	ATTCAATTCATACAG[A/G]AAAAACAAGATAAAT	5252
rs553183576	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409164	GAGCAAGACTCCGTC[C/T]CAACAACAACAACAA	5252
rs553949897	snp	A/G			synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415011	CCCTGGGGAAGCGCC[A/G]GAGGCCGGAGCCAGA	5252
rs554211449	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411732	TGTTAGTTACCGAGA[A/G]GAGAGCCAGTCACTA	5252
rs554273107	snp	A/G	0.000287699	0.0119903	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412269	CCAGGATGCAATGGC[A/G]CAGCCCCCCCGGCTG	5252
rs554324129	snp	G/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410019	CCCTCTGCTATCACC[G/T]GTTCTGGACCTTGGC	5252
rs554374549	snp	A/G	0.00159617	0.0282053	intron-variant	PHF1	GRCh38.p7	6:33413904	CCTCAGTTCTCCCAC[A/G]CCCTTCTCCACTCCA	5252
rs554712186	snp	A/G	3.30256e-05	0.00406346	intron-variant	PHF1	GRCh38.p7	6:33413164	CAAGCACACACAGGT[A/G]TGCAATAAGTGGTCT	5252
rs554795657	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415502	GGAAGGGAGTCCCTT[G/T]GGGGTAGTGTTTGAG	5252
rs554931552	snp	C/T	8.23621e-05	0.00641672	intron-variant	PHF1	GRCh38.p7	6:33412429	ATCAAAAAGGTAAGA[C/T]CTTCTACCTCTGACC	5252
rs555058519	snp	C/T			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416286	CTTCATGATTCCTGA[C/T]CCCTCCCATCCTTCC	5252
rs555608864	snp	C/T	0.00199481	0.0315187	utr-variant-5-prime, nc-transcript-variant, intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411181	GTCTCCTACGTCTGC[C/T]CCTGCCCGGCTCCCG	5252
rs556394865	snp	A/G	0.000988793	0.022213	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413242	TCCAGCCCCTGGAGA[A/G]GGAGAGGGCACATCC	5252
rs556525016	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412175	TCAGGAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA	5252
rs556703274	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411710	GGTTTGGGGTCGGGG[A/G]GAGGGCTGTTAGTTA	5252
rs556963044	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409219	TGCCAGTGTCCTTTA[C/G]ACAGAACTCTAGTAG	5252
rs557341857	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416400	AGGATGATAAGGGAT[C/T]CCGGACTCTGTATGA	5252
rs557993023	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409392	TACAGGGTATTGCTG[C/G]AAATGAAAGCCTCCT	5252
rs558515434	snp	A/C	0.00119737	0.0244387	intron-variant	PHF1	GRCh38.p7	6:33413933	CAGTCTCTTCCCAAC[A/C]TCTGCAGCGTTACCT	5252
rs558572694	in-del	-/A	0.00795532	0.062565	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416544	AAACAGGCAAAAGGC[-/A]AGAGAGACCCAAAGA	5252
rs558765870	snp	C/T	0.000798403	0.0199641	intron-variant	KIFC1	GRCh38.p7	6:33408538	TGCATTGGTTAGTCA[C/T]GATTCTTTTATGAAG	5252
rs559843500	snp	A/G	0.000798403	0.0199641	intron-variant	PHF1	GRCh38.p7	6:33412878	CTGGCCTTAGTCCCC[A/G]AGCCACTGCTCTGGC	5252
rs560487735	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410054	ATCATCTTCCCCTCT[C/G]CTAATACCCCCTACC	5252
rs560729750	snp	C/G	1.65403e-05	0.00287574	intron-variant	PHF1	GRCh38.p7	6:33413378	CCTCTCCCCACCCCT[C/G]TGAAGCCACCCACCT	5252
rs561383534	snp	G/T			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411241	GGCAGGAGGCGCTGG[G/T]GGGGGGCAGGGAGCC	5252
rs561803565	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411846	ACAGATACTTCATTC[C/T]TGATGGCAAAATAGG	5252
rs561929268	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410206	GTGGGTGTCGGCAAA[C/T]GGGGACCGGACCCCA	5252
rs561932287	snp	C/G	3.72592e-05	0.00431604	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416149	ACCGGCACTTTCATA[C/G]CCTGACCTCTGACCT	5252
rs561938069	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409588	ATGGGAGATCTTGGG[A/G]AAAATGTTGTATTGG	5252
rs562553185	snp	A/C	0.000131789	0.00811648	intron-variant	PHF1	GRCh38.p7	6:33412616	GAGACCTGAGATTGC[A/C]CATCCCATGGAAAAC	5252
rs562692722	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412034	AGGCATGGTGGCATG[C/T]GCCTGTAATCCCACC	5252
rs562814276	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33409973	TTTACGTGGGAGGCG[A/G]GAGCGGGGGCTGAGG	5252
rs563209891	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415407	TTATCACCCAGAATT[A/C]TTTTCCCTCTCCCCC	5252
rs563470498	snp	A/C	0.000264271	0.011492	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416661	CTCATCATGGCAGGA[A/C]TGTGATAGAGTCAGA	5252
rs563918425	snp	G/T	1.67125e-05	0.00289067	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415911	CATCCCCATCCCCAG[G/T]TCTTCCTAGACGCTC	5252
rs564266452	snp	C/T	0.000184802	0.00961076	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416119	CTGCCTCTGCCCAGC[C/T]CCCCATTCACACACA	5252
rs564342412	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33408899	ACCTCCTGGCCGGGC[A/G]CGGTGGCTCATGCCT	5252
rs564401607	snp	C/G	0.0375182	0.131725	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409709	CGGATCCAGATCTGT[C/G]TGTGTGTGTGTGTGT	5252
rs565605882	snp	A/G	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33413627	AGGAAATGAAGGAAA[A/G]AGAACAGGATGAGGG	5252
rs565691549	snp	C/T			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411462	CCTGACATAACCTGG[C/T]ACCAGGATGATTGTT	5252
rs565756929	snp	A/G	0.00119737	0.0244387	intron-variant	PHF1	GRCh38.p7	6:33414886	AGTCCTGGGGGGTAT[A/G]TGTATAGAGATGGGG	5252
rs565996743	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415419	ATTCTTTTCCCTCTC[C/T]CCCTTGGCTACCCAC	5252
rs566086431	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	PHF1, KIFC1	GRCh38.p7	6:33410719	GCATGGGGCGGGGGA[C/G]CAGGCCGGAGGCGGG	5252
rs566272716	snp	C/G	0.000869798	0.0208361	intron-variant	PHF1	GRCh38.p7	6:33413848	TGAGACCAAGGCAGA[C/G]TCTCTAGGAGCCAAG	5252
rs567251933	snp	A/G	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33412986	CTTTGCAGGCAGAAG[A/G]TGGTTTAAATGCATC	5252
rs567871066	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411242	GCAGGAGGCGCTGGT[A/G]GGGGGCAGGGAGCCG	5252
rs567899409	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412141	CACTCTGGCCTGGGC[A/G]ACAGAGCAAAACTCC	5252
rs568067910	snp	C/T	4.94491e-05	0.00497213	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416768	GCCACTTCGTAAGGG[C/T]GCACAGAACTACAAA	5252
rs568194621	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409177	TCTCAACAACAACAA[A/C]AAAAAAAAGAGCCTC	5252
rs568201930	in-del	-/GGAGGGCGGGGCTGGGGCTAACAGCGAGT	0.0810805	0.184299	upstream-variant-2KB, downstream-variant-500B	PHF1, KIFC1	GRCh38.p7	6:33410570	CGCGACTCGTCACGG[lengthTooLong]GGAGGGCGGGGCGCG	5252
rs568257489	snp	C/T	0.00438332	0.0466095	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409754	GTGTGTGTGTGTGTG[C/T]CCCTATGTCTATGTA	5252
rs568885830	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410381	GGTCCTCGCGCCCTT[C/G]GTCTGCGCCAGCCCT	5252
rs569701786	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415550	GGAGAAGGTCCTGTT[A/C]CCCTGCTTCAGGTCC	5252
rs569846417	snp	A/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416403	ATGATAAGGGATCCC[A/G]GACTCTGTATGATTG	5252
rs569969548	snp	C/T	0.000798403	0.0199641	intron-variant	KIFC1	GRCh38.p7	6:33408522	CTAATCTTAGTTGTT[C/T]TGCATTGGTTAGTCA	5252
rs570166629	snp	G/T	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33414668	GATTGAGGAATGGCG[G/T]AAGGAGGAACCGTTT	5252
rs570442473	snp	A/G			utr-variant-3-prime, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415903	CTCAGTTTCATCCCC[A/G]TCCCCAGGTCTTCCT	5252
rs570615932	snp	C/T	0.000399281	0.0141238	intron-variant	KIFC1	GRCh38.p7	6:33408571	ATTTGCCTTGCCATC[C/T]ACTTGGTTTCTCTGA	5252
rs571764561	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412188	AAAAAAAAGAAAAAG[A/G]AAATGGGGAAGGTTT	5252
rs571858795	snp	G/T	1.65622e-05	0.00287764	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413288	TGTGTCTTTGCGATC[G/T]CCACCAAGGTAAAGG	5252
rs571867105	snp	C/T	1.64727e-05	0.00286986	intron-variant	PHF1	GRCh38.p7	6:33414131	TGGATTGGGCATGAC[C/T]TCAGTGTAACTCCAC	5252
rs571936645	snp	A/C	6.62449e-05	0.00575483	intron-variant	PHF1	GRCh38.p7	6:33413578	TAATGAGAGGGGAGC[A/C]GACTGTGGAATGAAT	5252
rs572430160	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411766	TTGGAAGAGGACTCA[A/G]AAAGCTGGTGATGGG	5252
rs572492088	snp	C/T	0.000117963	0.00767904	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412279	ATGGCGCAGCCCCCC[C/T]GGCTGAGCCGCTCTG	5252
rs572688267	in-del	-/G	0.00373375	0.0430457	intron-variant	PHF1	GRCh38.p7	6:33414399	TTTGGGGGTTGGGAT[-/G]GGACAGGGAGATGTA	5252
rs573121142	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409553	TTCGGTATTTCTGAG[C/G]GCAGCCCTAGCATTG	5252
rs573233225	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409894	TTATTAGCATTTGCC[A/C]AAGAAGGCAGATACT	5252
rs573890468	snp	C/T	0.0017446	0.0294831	intron-variant	PHF1	GRCh38.p7	6:33412463	TTCCTAGTTCCCTTA[C/T]CTAATTCTGGTTCCC	5252
rs574314174	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416294	TTCCTGACCCCTCCC[A/G]TCCTTCCCATTTCCT	5252
rs574507779	snp	A/G	0.000399281	0.0141238	intron-variant	KIFC1	GRCh38.p7	6:33408617	GGAAAAACAAGATAA[A/G]TGCTGAATTATTTAT	5252
rs575126599	snp	A/C/T	6.85065e-05	0.00585228	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415790	TCTGCCCATTTCTTA[A/C/T]AATTGCCTTCTCTCC	5252
rs575508989	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416447	TAAACAAATCTAGCA[G/T]CTCTGAGTCATTCTG	5252
rs575713052	snp	C/T	3.32718e-05	0.00407858	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415949	CCTTCTCCCCTGTGC[C/T]GTAGTTTGTCTCCTG	5252
rs576030935	snp	C/T	0.000399281	0.0141238	intron-variant	PHF1	GRCh38.p7	6:33414170	ATTTCACTCTATATG[C/T]CCCAACCTCCCACCT	5252
rs576149310	in-del	-/A	0.347694	0.230122	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412165	AAACTCCATCTCAGG[-/A]AAAAAAAAAAAAAAA	5252
rs576352183	snp	C/T			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411556	GGTCCCAAAACACGT[C/T]TCTGGGCAACAGGAC	5252
rs577558781	snp	C/T	0.000798403	0.0199641	intron-variant	PHF1	GRCh38.p7	6:33413941	TCCCAACCTCTGCAG[C/T]GTTACCTCACCTGTT	5252
rs578220541	in-del	-/CAA			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409165	AGCAAGACTCCGTCT[-/CAA]CAACAACAACAAAAA	5252
rs745306727	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412525	GGACAGTGCTAGGGA[A/G]GTGTGTCTGGTCCAG	5252
rs745324138	snp	A/G			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409161	ACAGAGCAAGACTCC[A/G]TCTCAACAACAACAA	5252
rs745357840	in-del	-/TC	1.7134e-05	0.00292689	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415793	CCCATTTCTTACAAT[-/TC]TGCCTTCTCTCCCTA	5252
rs745430478	snp	A/G	1.64754e-05	0.00287009	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416889	ACCCACACAGTACAC[A/G]CCCTCACCCCATCCA	5252
rs745515393	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414530	CCTCTCTGCTCTTAA[C/T]AGCCACAAGGACCGG	5252
rs745625082	snp	A/G	1.72561e-05	0.0029373	missense, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415810	GCCTTCTCTCCCTAG[A/G]TCACCCCTGGAACTT	5252
rs745694970	snp	A/G	4.9445e-05	0.00497193	intron-variant	PHF1	GRCh38.p7	6:33414417	ACAGGGAGATGTAGC[A/G]GAAAGGGGAAGAGAA	5252
rs745702287	snp	C/T	3.33868e-05	0.00408562	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415917	CATCCCCAGGTCTTC[C/T]TAGACGCTCAGCACC	5252
rs745757386	in-del	-/CACTTTGGGAA	1.64749e-05	0.00287005	intron-variant	PHF1	GRCh38.p7	6:33414198	CTCAGGACTCCCCTG[-/CACTTTGGGAA]GCTCTTAAAATGCCT	5252
rs745807018	snp	A/C	1.65176e-05	0.00287376	intron-variant	PHF1	GRCh38.p7	6:33413401	ACCCACCTGTCCTGT[A/C]TCTGCAGAGGGGAGG	5252
rs745852424	snp	C/G	1.64741e-05	0.00286998	missense, upstream-variant-2KB, utr-variant-3-prime	KIFC1, PHF1	GRCh38.p7	6:33409687	TCAGGCCAACAGGAA[C/G]TGAAGACGGATCCAG	5252
rs745886202	snp	A/G	1.67747e-05	0.00289605	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416590	GCCCAGTCATCACCT[A/G]GAAGTCAGAAGGCGT	5252
rs745985002	snp	A/G	0.000139753	0.00835804	intron-variant	PHF1	GRCh38.p7	6:33414911	ATGGGGAGGTCTTGG[A/G]GGTGTCCGGGAGGGG	5252
rs746094945	snp	C/T	1.71855e-05	0.00293129	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412218	TCTCAGCATTCATAA[C/T]CTTCTCCTCCCCATT	5252
rs746185630	snp	C/G	1.67276e-05	0.00289197	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415337	CTGCCCAGGTCAGTG[C/G]TCCTCTGCCCCTCCC	5252
rs746260495	snp	C/T	1.64939e-05	0.0028717	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409698	GGAAGTGAAGACGGA[C/T]CCAGATCTGTGTGTG	5252
rs746328453	in-del	-/C			intron-variant	KIFC1	GRCh38.p7	6:33408657	GTATTGAGTTGATAT[-/C]CTAGCAGCTTCCAAA	5252
rs746367583	snp	C/T	3.29478e-05	0.00405867	intron-variant, missense, nc-transcript-variant, utr-variant-3-prime	PHF1	GRCh38.p7	6:33415236	GCCCCCTCTTCTAGG[C/T]CTCAGTGTCTCCACC	5252
rs746467163	snp	C/T	1.64773e-05	0.00287026	intron-variant	PHF1	GRCh38.p7	6:33414384	AAGGGGTAGTGCAGT[C/T]TTGGGGGTTGGGATG	5252
rs746510816	in-del	-/C	5.14201e-05	0.00507024	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412249	TCTTTTCTGGCTAGG[-/C]CCCCCCAGGATGCAA	5252
rs746555129	snp	C/T	1.6473e-05	0.00286988	intron-variant	PHF1	GRCh38.p7	6:33412436	AGGTAAGACCTTCTA[C/T]CTCTGACCTTCTTCC	5252
rs746635975	snp	A/C/T	3.29485e-05	0.00405874	intron-variant	PHF1	GRCh38.p7	6:33414193	TCCCACCTCAGGACT[A/C/T]CCCTGGCTCTTAAAA	5252
rs746672037	in-del	-/GTAA	4.94262e-05	0.00497098	intron-variant	PHF1	GRCh38.p7	6:33414007	GCACAGTTTTCCTGT[-/GTAA]GTGTGTTTGCTCCCT	5252
rs746948151	snp	C/T	1.65056e-05	0.00287272	intron-variant	PHF1	GRCh38.p7	6:33413181	GCAATAAGTGGTCTA[C/T]TATTATCACTGCAGC	5252
rs747030972	snp	A/C	1.64735e-05	0.00286993	synonymous-codon, upstream-variant-2KB, utr-variant-3-prime	KIFC1, PHF1	GRCh38.p7	6:33409682	ACTGCTCAGGCCAAC[A/C]GGAAGTGAAGACGGA	5252
rs747076466	in-del	-/TGTGTGTGTGTG			cds-indel, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409706	AGACGGATCCAGATC[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT	5252
rs747118982	snp	C/G	0.000324403	0.0127317	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409733	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs747186476	snp	A/G			missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415845	TTGGTTTCCCCACAG[A/G]CATCCCTAAAAGTGC	5252
rs747219842	snp	C/G	3.71789e-05	0.00431139	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416141	TCACACACACCGGCA[C/G]TTTCATACCCTGACC	5252
rs747251422	snp	C/T	1.64741e-05	0.00286998	intron-variant, missense, synonymous-codon	PHF1	GRCh38.p7	6:33415225	CTCAGTCCTTTGCCC[C/T]CTCTTCTAGGCCTCA	5252
rs747346531	snp	C/G	3.29592e-05	0.00405938	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416877	CCAGCAAGTCACACC[C/G]ACACAGTACACACCC	5252
rs747417262	snp	C/T	1.65037e-05	0.00287256	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413442	AAGGGCCCCTATGCC[C/T]GGGCCATGCTGGGTA	5252
rs747440623	snp	A/C	0.000230624	0.0107359	intron-variant, missense, stop-gained	PHF1	GRCh38.p7	6:33415222	TCTCTCAGTCCTTTG[A/C]CCCCTCTTCTAGGCC	5252
rs747445516	snp	A/G	4.94173e-05	0.00497053	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412514	CCATTCCAGGTGGAC[A/G]GTGCTAGGGAGGTGT	5252
rs747642866	snp	C/T	3.29728e-05	0.00406021	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415587	TCCCCACTCCAACCC[C/T]AGCAGCCCCATCCGG	5252
rs747716478	in-del	-/GTGTGTGTG	0.000174496	0.00933903	cds-indel, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409737	TGTGTGTGTGTGTGT[-/GTGTGTGTG]TGTGTGTGTCCCTAT	5252
rs747733929	snp	C/G	1.6473e-05	0.00286988	intron-variant	PHF1	GRCh38.p7	6:33414143	GACCTCAGTGTAACT[C/G]CACACCACAGTATTT	5252
rs747761877	snp	C/G	1.71249e-05	0.00292612	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415354	CCTCTGCCCCTCCCC[C/G]ACAAAATATGCTCCC	5252
rs747840400	in-del	-/GTGTG	7.33703e-05	0.00605638	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409710	GATCCAGATCTGTGT[-/GTGTG]GTGTGTGTGTGTGTG	5252
rs747879466	snp	A/G	1.82424e-05	0.00302007	intron-variant	PHF1	GRCh38.p7	6:33414881	GTGTTAGTCCTGGGG[A/G]GTATATGTATAGAGA	5252
rs747911697	snp	C/T	1.66048e-05	0.00288134	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412762	TGTGGTCCCTGGGAA[C/T]CGGCTGGTCAGCTGT	5252
rs748072500	snp	C/T	1.66496e-05	0.00288522	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414725	CTCTTCTTGCCCCAG[C/T]TTCATTTCAGGGAGA	5252
rs748119733	snp	C/T	1.6501e-05	0.00287232	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413419	TGCAGAGGGGAGGTG[C/T]CCTGAAGAAGGGCCC	5252
rs748340965	in-del	-/C	1.65272e-05	0.0028746	frameshift-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416656	CAGGGCTCATCATGG[-/C]AGGACTGTGATAGAG	5252
rs748454683	snp	A/G	9.88338e-05	0.00702902	intron-variant	PHF1	GRCh38.p7	6:33412425	TACCATCAAAAAGGT[A/G]AGACCTTCTACCTCT	5252
rs748572233	snp	C/T	2.32523e-05	0.00340963	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415073	GAGGAGCTGGGGCCA[C/T]CCTCAGCAGTGCGCA	5252
rs748597388	snp	C/G/T	4.94404e-05	0.00497173	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416757	CAATTACCTCGGCCA[C/G/T]TTCGTAAGGGTGCAC	5252
rs748650664	snp	C/T	3.3168e-05	0.00407221	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412299	GAGCCGCTCTGGTGC[C/T]TCCTCACTTTGGGAC	5252
rs748759190	snp	A/G	1.64746e-05	0.00287002	intron-variant, synonymous-codon, nc-transcript-variant, missense, utr-variant-3-prime	PHF1	GRCh38.p7	6:33415270	CCCCAGCCCTAACCA[A/G]AGTTACCAGGGCAGC	5252
rs748849199	snp	C/G	1.6981e-05	0.00291379	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415348	AGTGCTCCTCTGCCC[C/G]TCCCCCACAAAATAT	5252
rs748862084	snp	C/T			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409028	AAAAAATTCACCGGG[C/T]GTGGTGGCGGGCGCC	5252
rs748908747	snp	C/G	1.64754e-05	0.00287009	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416896	CAGTACACACCCTCA[C/G]CCCATCCATCTCAAA	5252
rs749063381	snp	A/G	1.64773e-05	0.00287026	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414540	CTTAACAGCCACAAG[A/G]ACCGGTGAGTTGGAG	5252
rs749075092	in-del	-/TT	4.94214e-05	0.00497074	intron-variant	PHF1	GRCh38.p7	6:33414230	TGTGGTCTTGAAAAC[-/TT]TGTTTTTCCAGGGTG	5252
rs749143205	snp	G/T	3.29489e-05	0.00405874	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412572	AGTTTCTGGTTCTAT[G/T]GAAAGACATTAGCCC	5252
rs749240796	in-del	-/GCCTCTGCCCA	3.67742e-05	0.00428786	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416106	TCTTCTGAACAGCCT[-/GCCTCTGCCCA]GCTCCCCATTCACAC	5252
rs749253646	snp	A/T	1.66715e-05	0.00288712	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415925	GGTCTTCCTAGACGC[A/T]CAGCACCCCCTTCTC	5252
rs749259966	snp	G/T			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416242	ATCCAAGAGTGGGGA[G/T]TGGGGAAGAGGCCCT	5252
rs749282964	snp	C/T	2.88838e-05	0.00380014	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415064	GGGAAAGTGGAGGAG[C/T]TGGGGCCACCCTCAG	5252
rs749385130	in-del	-/G			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409733	TGTGTGTGTGTGTGT[-/G]TGTGTGTGTGTGTGT	5252
rs749532796	snp	C/T	0.000720202	0.0189626	intron-variant	PHF1	GRCh38.p7	6:33414929	TGTCCGGGAGGGGGC[C/T]GGGGGGATAAGGAGG	5252
rs749545694	snp	C/T	1.71281e-05	0.00292639	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412228	CATAACCTTCTCCTC[C/T]CCATTTCTTTTCTGG	5252
rs749684955	snp	C/T	5.01576e-05	0.00500762	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412288	CCCCCCCGGCTGAGC[C/T]GCTCTGGTGCCTCCT	5252
rs749691601	in-del	-/TGA	3.29772e-05	0.00406048	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415695	GTCTTCTATTACCAG[-/TGA]TGATGCTCTTCTTCC	5252
rs749791794	snp	C/T	3.29881e-05	0.00406115	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415575	AGGTCCTGACTTTCC[C/T]CACTCCAACCCCAGC	5252
rs749793990	snp	A/G	1.64757e-05	0.00287012	intron-variant	PHF1	GRCh38.p7	6:33414009	ACAGTTTTCCTGTGT[A/G]AGTGTGTTTGCTCCC	5252
rs749845193	snp	A/G	3.71299e-05	0.00430854	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416137	CCATTCACACACACC[A/G]GCACTTTCATACCCT	5252
rs749898538	snp	A/G	1.67108e-05	0.00289052	intron-variant	PHF1	GRCh38.p7	6:33414701	TACAGCACTGACCCT[A/G]TATCATTTCTCTTCT	5252
rs750051027	snp	A/G			intron-variant	PHF1	GRCh38.p7	6:33413614	GGTGGTGGATCCCAG[A/G]AAATGAAGGAAAAAG	5252
rs750054892	snp	C/G	0.00046114	0.0151775	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409723	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs750089367	snp	A/C/G	5.00474e-05	0.00500216	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33416010	GTTACCTGTCCCGAG[A/C/G]GGACCCTGTCCGGGT	5252
rs750111165	in-del	-/GT	3.295e-05	0.00405881	intron-variant	PHF1	GRCh38.p7	6:33414011	AGTTTTCCTGTGTAA[-/GT]GTGTTTGCTCCCTCT	5252
rs750120408	snp	A/G	4.96701e-05	0.00498323	intron-variant	PHF1	GRCh38.p7	6:33413571	GAGTGAGTAATGAGA[A/G]GGGAGCAGACTGTGG	5252
rs750247676	snp	A/G	1.6473e-05	0.00286988	missense, upstream-variant-2KB, utr-variant-3-prime	KIFC1, PHF1	GRCh38.p7	6:33409646	ACCCCCTGCCCCCAG[A/G]TGAACCAGTGTGTTA	5252
rs750254835	snp	A/G	1.65411e-05	0.00287581	synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33413811	CCAGTGTCTGAGCAA[A/G]CCCCTCCTCTATGGG	5252
rs750314754	snp	A/G	3.29495e-05	0.00405877	intron-variant	PHF1	GRCh38.p7	6:33415200	TGTGGGAAGGAGTCA[A/G]GGATTATCTCTCAGT	5252
rs750410487	snp	C/T	1.68792e-05	0.00290505	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412275	TGCAATGGCGCAGCC[C/T]CCCCGGCTGAGCCGC	5252
rs750544202	snp	C/G	1.64776e-05	0.00287028	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412366	CGGCTTTGGGAGGGT[C/G]AAGATGTGCTGGCCA	5252
rs750592337	snp	A/C			intron-variant	KIFC1	GRCh38.p7	6:33408507	TAAATGGGGATTTTT[A/C]TAATCTTAGTTGTTC	5252
rs750600236	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414107	GAGACTACAGCTTCG[C/T]TGGTGAGCTGGATTG	5252
rs750635400	snp	A/C	1.648e-05	0.0028705	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415664	GGGACAGTGGACCCC[A/C]AGACAGGTGAGATTC	5252
rs750829355	snp	C/G	1.65075e-05	0.00287289	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415553	GAAGGTCCTGTTCCC[C/G]TGCTTCAGGTCCTGA	5252
rs750836542	in-del	-/C	1.65507e-05	0.00287664	intron-variant	PHF1	GRCh38.p7	6:33413363	TCTCCCAAGCCTTTT[-/C]CTCTCCCCACCCCTC	5252
rs750926987	snp	A/C	1.65162e-05	0.00287365	intron-variant	PHF1	GRCh38.p7	6:33413147	TATTCCTGTCCCAAT[A/C]CCAAGCACACACAGG	5252
rs751003147	in-del	-/TGTGTGTGTGTGTGTGTGTT	1.80279e-05	0.00300227	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409733	GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTGTT]TGTGTGTGTGTGTGT	5252
rs751052204	snp	C/T	1.67874e-05	0.00289714	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415896	CATCTTCCTCAGTTT[C/T]ATCCCCATCCCCAGG	5252
rs751193737	snp	C/T	1.65485e-05	0.00287645	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413549	CTGTTACTGTGGTGG[C/T]CCTGGGGAGTGAGTA	5252
rs751239683	snp	C/T			missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414805	CCCCTGTGGAGCCCC[C/T]TACTGGAGATGGAGC	5252
rs751268972	snp	A/C	1.64746e-05	0.00287002	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409614	ATTGGTTACGCTGCA[A/C]ACTTTTATCCTGTCT	5252
rs751391590	snp	C/T	1.65209e-05	0.00287405	intron-variant	PHF1	GRCh38.p7	6:33413396	AAGCCACCCACCTGT[C/T]CTGTCTCTGCAGAGG	5252
rs751587198	snp	A/G	1.65187e-05	0.00287386	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415542	TCCCAGGGGGAGAAG[A/G]TCCTGTTCCCCTGCT	5252
rs751618943	snp	A/C	1.68442e-05	0.00290204	intron-variant	PHF1	GRCh38.p7	6:33413862	ACTCTCTAGGAGCCA[A/C]GGATGCCCTCTTTCT	5252
rs751643353	snp	C/T			intron-variant	KIFC1	GRCh38.p7	6:33408595	TCTCTGAAATTCAAT[C/T]CATACAGGAAAAACA	5252
rs751655335	in-del	-/G	0.0100768	0.0702628	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409731	TGTGTGTGTGTGTGT[-/G]TGTGTGTGTGTGTGT	5252
rs751708549	snp	A/C	1.64727e-05	0.00286986	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414085	GCGGGGGCCCTGAGA[A/C]AGTCCGGAGACTACA	5252
rs751885991	in-del	-/CCCA	0.000182846	0.00955978	intron-variant	PHF1	GRCh38.p7	6:33413320	CTTCCCTGTTACCCT[-/CCCA]TCCTGTGGGAGCCTC	5252
rs751889544	snp	G/T	1.64993e-05	0.00287218	intron-variant	PHF1	GRCh38.p7	6:33412649	ACCTGGCCTAGAGGG[G/T]CAGAAAGAGACTTAA	5252
rs751896764	snp	C/G	3.34588e-05	0.00409002	intron-variant	PHF1	GRCh38.p7	6:33412830	ATGGTCCAGCTTGCT[C/G]TTCCCTCCAGGATGG	5252
rs752059822	in-del	-/TC	0.206197	0.248458	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409703	GAAGACGGATCCAGA[-/TC]TCTGTGTGTGTGTGT	5252
rs752080996	snp	C/T	3.34969e-05	0.00409235	intron-variant	PHF1	GRCh38.p7	6:33414688	AGGAACCGTTTTTTA[C/T]AGCACTGACCCTATA	5252
rs752206962	snp	A/C			intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415758	ACTGTTTCTCTGATT[A/C]ACATGTGCTCTCCAT	5252
rs752320698	snp	A/G	5.65041e-05	0.00531496	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415089	CCTCAGCAGTGCGCA[A/G]TCAGCCCGAGCCCCA	5252
rs752400963	snp	C/G/T	6.61529e-05	0.00575083	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416819	GATCACTCAAAGATT[C/G/T]ACCCAAAAGAACCCA	5252
rs752516914	snp	A/G	3.37069e-05	0.00410516	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415018	GAAGCGCCGGAGGCC[A/G]GAGCCAGAGCCCCTG	5252
rs752519101	snp	A/G	1.64825e-05	0.00287071	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416714	ACCCACTGCAGGTAC[A/G]GAAAGTTCCCCTGTT	5252
rs752662731	snp	A/G	1.69847e-05	0.00291411	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412272	GGATGCAATGGCGCA[A/G]CCCCCCCGGCTGAGC	5252
rs752808242	in-del	-/GTG	1.96069e-05	0.00313098	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409720	TGTGTGTGTGTGTGT[-/GTG]GTGTGTGTGTGTGTG	5252
rs752854917	snp	A/C	1.64901e-05	0.00287137	intron-variant, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415305	GCTACAACTTCCGGC[A/C]CACAGATGCCCGCTG	5252
rs752897237	snp	C/T	1.64757e-05	0.00287012	intron-variant	PHF1	GRCh38.p7	6:33412622	TGAGATTGCACATCC[C/T]ATGGAAAACAAACCT	5252
rs753022895	snp	G/T	1.64917e-05	0.00287151	intron-variant	PHF1	GRCh38.p7	6:33414590	AGGCTCGGAAAGAGA[G/T]GGAGAGTGGAAGCCT	5252
rs753037757	snp	A/G	3.29473e-05	0.00405864	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414495	TCAGACACCCCCAAA[A/G]GAGAACGTTCTTCCA	5252
rs753093450	snp	A/G	1.64727e-05	0.00286986	intron-variant	PHF1	GRCh38.p7	6:33412501	CCTGTTTGCTCACCC[A/G]TTCCAGGTGGACAGT	5252
rs753219003	snp	A/G	1.7056e-05	0.00292022	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415008	GTCCCCTGGGGAAGC[A/G]CCGGAGGCCGGAGCC	5252
rs753309306	snp	A/G	3.30169e-05	0.00406293	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413263	GGGCACATCCTGGGT[A/G]TGCCGCCAGTGTGTC	5252
rs753340823	snp	A/G	1.65149e-05	0.00287353	intron-variant	PHF1	GRCh38.p7	6:33413158	CAATACCAAGCACAC[A/G]CAGGTATGCAATAAG	5252
rs753472290	snp	C/T	1.65649e-05	0.00287788	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416635	GATCTTCATGATGAG[C/T]AGGAACAGGGCTCAT	5252
rs753516195	snp	A/T	5.16524e-05	0.00508169	intron-variant	PHF1	GRCh38.p7	6:33414857	GGGGGGATGGGGGAA[A/T]TTCTCAGGGTGTTAG	5252
rs753567710	snp	C/G			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412138	CTGCACTCTGGCCTG[C/G]GCGACAGAGCAAAAC	5252
rs753675237	snp	C/G	3.4071e-05	0.00412727	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412254	TCTGGCTAGGCCCCC[C/G]CAGGATGCAATGGCG	5252
rs753675802	snp	A/T	1.85924e-05	0.00304891	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416142	CACACACACCGGCAC[A/T]TTCATACCCTGACCT	5252
rs753802434	snp	A/T	1.6715e-05	0.00289089	intron-variant	PHF1	GRCh38.p7	6:33413845	AGGTGAGACCAAGGC[A/T]GACTCTCTAGGAGCC	5252
rs753892070	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414071	ATGCTGTGTGTGTCG[C/T]GGGGGCCCTGAGAAA	5252
rs753975753	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412410	GCTGCTATACTTGGG[C/T]ACCATCAAAAAGGTA	5252
rs753990972	snp	A/C	1.73021e-05	0.00294121	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415101	GCAATCAGCCCGAGC[A/C]CCAGGAGCAGAGGGA	5252
rs754036775	snp	C/G	4.94214e-05	0.00497074	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414490	AGCTTTCAGACACCC[C/G]CAAAGGAGAACGTTC	5252
rs754145165	snp	C/T	1.64961e-05	0.00287189	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415710	GTGATGCTCTTCTTC[C/T]CCTCTATGTGCTCAA	5252
rs754147771	snp	C/T	1.6473e-05	0.00286988	intron-variant	PHF1	GRCh38.p7	6:33412487	GGTTCCCATTTCATC[C/T]TGTTTGCTCACCCAT	5252
rs754183129	snp	C/T	3.41746e-05	0.00413354	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415860	ACATCCCTAAAAGTG[C/T]CCCCCACTCGATGAC	5252
rs754209007	in-del	-/TG	8.28315e-05	0.00643497	intron-variant	PHF1	GRCh38.p7	6:33413582	GAGAGGGGAGCAGAC[-/TG]TGGAATGAATGATGT	5252
rs754232931	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414350	CTGAGAATTGGGACA[A/G]TTTGCTCCTGGGGGA	5252
rs754410970	in-del	-/G	1.64746e-05	0.00287002	intron-variant, frameshift-variant	PHF1	GRCh38.p7	6:33415221	ATCTCTCAGTCCTTT[-/G]CCCCCTCTTCTAGGC	5252
rs754470379	snp	G/T	1.65247e-05	0.00287438	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413272	CTGGGTATGCCGCCA[G/T]TGTGTCTTTGCGATC	5252
rs754694108	snp	C/T			missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414822	ACTGGAGATGGAGCA[C/T]TCACCAGGTCACTGG	5252
rs754780335	snp	A/C	0.000164736	0.0090742	intron-variant	PHF1	GRCh38.p7	6:33412609	GACTCTAGAGACCTG[A/C]GATTGCACATCCCAT	5252
rs754795988	snp	C/T	1.7809e-05	0.00298398	intron-variant	PHF1	GRCh38.p7	6:33414874	TCTCAGGGTGTTAGT[C/T]CTGGGGGGTATATGT	5252
rs754941553	snp	A/C/T	3.40526e-05	0.00412618	utr-variant-3-prime, synonymous-codon, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33416033	GTCCGGGTCCTTGCT[A/C/T]GGAGAGTACGGCCTG	5252
rs754957825	snp	C/G	0.0415516	0.138019	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409729	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs755087665	snp	A/G	1.70461e-05	0.00291938	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415106	CAGCCCGAGCCCCAG[A/G]AGCAGAGGGAGCGGG	5252
rs755089802	snp	A/G	1.64958e-05	0.00287187	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416797	AAATAGGTGGGTGGG[A/G]GAAGGGGATCACTCA	5252
rs755207501	snp	A/C	1.64727e-05	0.00286986	intron-variant	PHF1	GRCh38.p7	6:33412497	TCATCCTGTTTGCTC[A/C]CCCATTCCAGGTGGA	5252
rs755270956	in-del	-/G	1.65066e-05	0.0028728	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415555	AGGTCCTGTTCCCCT[-/G]CTTCAGGTCCTGACT	5252
rs755286224	snp	C/T	1.64803e-05	0.00287052	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416751	GCAATGCAATTACCT[C/T]GGCCACTTCGTAAGG	5252
rs755305585	snp	A/G	1.6477e-05	0.00287024	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414364	AGTTTGCTCCTGGGG[A/G]AGGTAAGGGGTAGTG	5252
rs755395304	in-del	-/G	1.68309e-05	0.00290089	intron-variant	PHF1	GRCh38.p7	6:33413696	GACAGTTATGGGGAA[-/G]GGGGTTTCTGGAGGC	5252
rs755448100	snp	A/T	8.24355e-05	0.00641957	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415583	ACTTTCCCCACTCCA[A/T]CCCCAGCAGCCCCAT	5252
rs755497922	snp	A/G	1.64727e-05	0.00286986	intron-variant	PHF1	GRCh38.p7	6:33414135	TTGGGCATGACCTCA[A/G]TGTAACTCCACACCA	5252
rs755620530	snp	G/T	1.71211e-05	0.00292579	intron-variant	PHF1	GRCh38.p7	6:33414849	CTGGTCCAGGGGGGA[G/T]GGGGGAAATTCTCAG	5252
rs755634963	in-del	-/C	1.71466e-05	0.00292797	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415795	CATTTCTTACAATTG[-/C]CCTTCTCTCCCTAGG	5252
rs755750355	snp	C/G	3.30311e-05	0.0040638	intron-variant	PHF1	GRCh38.p7	6:33413148	ATTCCTGTCCCAATA[C/G]CAAGCACACACAGGT	5252
rs755814526	snp	C/T	3.71478e-05	0.00430958	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416139	ATTCACACACACCGG[C/T]ACTTTCATACCCTGA	5252
rs755902943	snp	C/G	0.00698541	0.0586848	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409725	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs755927484	snp	C/T	3.33895e-05	0.00408579	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415918	ATCCCCAGGTCTTCC[C/T]AGACGCTCAGCACCC	5252
rs756096077	snp	A/G	3.29489e-05	0.00405874	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412374	GGAGGGTCAAGATGT[A/G]CTGGCCAGATGGACT	5252
rs756136957	snp	A/G	1.65304e-05	0.00287488	stop-lost, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416652	GGAACAGGGCTCATC[A/G]TGGCAGGACTGTGAT	5252
rs756365819	in-del	-/GTGTGTGTGTG	0.0377039	0.132024	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409735	TGTGTGTGTGTGTGT[-/GTGTGTGTGTG]TGTGTGTGTCCCTAT	5252
rs756452139	snp	A/G	1.65026e-05	0.00287246	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415562	GTTCCCCTGCTTCAG[A/G]TCCTGACTTTCCCCA	5252
rs756571844	snp	A/G/T	4.94176e-05	0.00497059	intron-variant	PHF1	GRCh38.p7	6:33414124	GGTGAGCTGGATTGG[A/G/T]CATGACCTCAGTGTA	5252
rs756648240	snp	A/T	1.67259e-05	0.00289183	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415338	TGCCCAGGTCAGTGC[A/T]CCTCTGCCCCTCCCC	5252
rs756666448	in-del	-/GAA	1.64993e-05	0.00287218	cds-indel, nc-transcript-variant	PHF1	GRCh38.p7	6:33413423	GAGGGGAGGTGCCCT[-/GAA]GAAGGGCCCCTATGC	5252
rs756686741	snp	A/C			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411594	TTATGATACCTCTAA[A/C]CTGAGTAGCCTTTGC	5252
rs756793916	snp	A/C/G	0.000512541	0.0160004	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414529	TCCTCTCTGCTCTTA[A/C/G]CAGCCACAAGGACCG	5252
rs756898331	snp	C/T	5.02298e-05	0.00501123	intron-variant	PHF1	GRCh38.p7	6:33414691	AACCGTTTTTTACAG[C/T]ACTGACCCTATATCA	5252
rs756913600	snp	A/C	1.64743e-05	0.00287	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409621	ACGCTGCAAACTTTT[A/C]TCCTGTCTAACCCCC	5252
rs756969430	in-del	-/TCT	1.64928e-05	0.00287161	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415702	TATTACCAGTGATGC[-/TCT]TCTTCCCCTCTATGT	5252
rs757018023	snp	C/T	1.65179e-05	0.00287379	intron-variant	PHF1	GRCh38.p7	6:33413398	GCCACCCACCTGTCC[C/T]GTCTCTGCAGAGGGG	5252
rs757039520	snp	A/G	4.94287e-05	0.00497111	intron-variant	PHF1	GRCh38.p7	6:33414377	GGGAGGTAAGGGGTA[A/G]TGCAGTTTTGGGGGT	5252
rs757060044	snp	A/C/G/T	0.000116565	0.00763362	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415934	AGACGCTCAGCACCC[A/C/G/T]CTTCTCCCCTGTGCC	5252
rs757078823	snp	A/G	3.93786e-05	0.00443709	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415049	AGGAGGAGGCAGAAG[A/G]GGAAAGTGGAGGAGC	5252
rs757103987	snp	A/G	1.65529e-05	0.00287683	intron-variant	PHF1	GRCh38.p7	6:33413560	GTGGCCCTGGGGAGT[A/G]AGTAATGAGAGGGGA	5252
rs757243741	snp	A/G	3.49638e-05	0.00418099	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415099	GCGCAATCAGCCCGA[A/G]CCCCAGGAGCAGAGG	5252
rs757256695	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414091	GCCCTGAGAAAGTCC[A/G]GAGACTACAGCTTCG	5252
rs757367487	snp	C/G	1.85153e-05	0.00304258	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409735	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs757457621	in-del	-/GTGTGTGTGTGTG	0.000848419	0.0205789	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409733	TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTG]TGTGTGTGTCCCTAT	5252
rs757475663	snp	C/T	1.69911e-05	0.00291466	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412273	GATGCAATGGCGCAG[C/T]CCCCCCGGCTGAGCC	5252
rs757629285	snp	A/G			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411970	GTTCGAGACCAGTTT[A/G]GCCAACATGGCCAAC	5252
rs757704342	snp	C/T	8.26508e-05	0.00642795	intron-variant, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415322	ACAGATGCCCGCTGC[C/T]TGCCCAGGTCAGTGC	5252
rs757705753	snp	A/G	1.65072e-05	0.00287286	intron-variant	PHF1	GRCh38.p7	6:33412671	GAGACTTAAAGGCAG[A/G]CCCTGTGACACTGTG	5252
rs757792573	snp	A/G	1.6476e-05	0.00287014	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416878	CAGCAAGTCACACCC[A/G]CACAGTACACACCCT	5252
rs757902427	snp	C/T	3.40541e-05	0.00412625	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415779	TGCTCTCCATTTCTG[C/T]CCATTTCTTACAATT	5252
rs757908269	snp	A/C	5.05446e-05	0.0050269	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415882	CTCGATGACTGCCTC[A/C]TCTTCCTCAGTTTCA	5252
rs758084721	snp	G/T			intron-variant	PHF1	GRCh38.p7	6:33413681	AAGTTTAGGGTTTGG[G/T]ACAGTTATGGGGAAG	5252
rs758154389	snp	A/G	5.01316e-05	0.00500632	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415039	AGAGCCCCTGAGGAG[A/G]AGGCAGAAGGGGAAA	5252
rs758264817	snp	A/G	1.68224e-05	0.00290016	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416575	CGGGATTTATTGGGG[A/G]CCCAGTCATCACCTG	5252
rs758476704	snp	A/C	3.29468e-05	0.00405861	missense, upstream-variant-2KB, utr-variant-3-prime	KIFC1, PHF1	GRCh38.p7	6:33409679	GGTACTGCTCAGGCC[A/C]ACAGGAAGTGAAGAC	5252
rs758521068	snp	C/G	1.65045e-05	0.00287263	intron-variant, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415314	TCCGGCCCACAGATG[C/G]CCGCTGCCTGCCCAG	5252
rs758714518	snp	C/T	1.64746e-05	0.00287002	intron-variant, synonymous-codon, missense	PHF1	GRCh38.p7	6:33415217	GATTATCTCTCAGTC[C/T]TTTGCCCCCTCTTCT	5252
rs758715932	snp	C/T	4.94173e-05	0.00497053	intron-variant	PHF1	GRCh38.p7	6:33412505	TTTGCTCACCCATTC[C/T]AGGTGGACAGTGCTA	5252
rs758734528	snp	G/T			intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415505	AGGGAGTCCCTTGGG[G/T]GTAGTGTTTGAGCTC	5252
rs758840002	snp	A/G	1.64735e-05	0.00286993	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414498	GACACCCCCAAAGGA[A/G]AACGTTCTTCCAGGC	5252
rs758841535	snp	A/G	3.29489e-05	0.00405874	intron-variant	PHF1	GRCh38.p7	6:33412623	GAGATTGCACATCCC[A/G]TGGAAAACAAACCTG	5252
rs759214198	snp	C/T	1.69387e-05	0.00291016	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412268	CCCAGGATGCAATGG[C/T]GCAGCCCCCCCGGCT	5252
rs759248161	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409718	ATCTGTGTGTGTGTG[-/T]GTGTGTGTGTGTGTG	5252
rs759352088	snp	C/G	1.64738e-05	0.00286995	intron-variant	PHF1	GRCh38.p7	6:33414233	GGTCTTGAAAACTTT[C/G]TTTTTCCAGGGTGGA	5252
rs759393949	snp	C/G	1.64762e-05	0.00287016	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415639	TCTGCCAGCACCGCA[C/G]GGACCTCTGGGGACA	5252
rs759428242	snp	C/T	1.65192e-05	0.00287391	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412325	GGGACCCAGCTTCTC[C/T]TGCTCCCACCTCTGG	5252
rs759534731	in-del	-/A	1.65002e-05	0.00287225	intron-variant	PHF1	GRCh38.p7	6:33412653	GGCCTAGAGGGGCAG[-/A]AAGAGACTTAAAGGC	5252
rs759548466	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414072	TGCTGTGTGTGTCGC[A/G]GGGGCCCTGAGAAAG	5252
rs759560184	snp	A/G	1.65943e-05	0.00288043	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414781	TTGGTCTCCATGCTC[A/G]GATGCCTCCCCCTGT	5252
rs759664324	snp	G/T	1.6638e-05	0.00288422	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412770	CTGGGAACCGGCTGG[G/T]CAGCTGTGAGAAGTG	5252
rs759731623	in-del	-/AAAC			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416433	GAAATAAAGAGAAAT[-/AAAC]AAATCTAGCAGCTCT	5252
rs759759817	snp	A/G	4.94189e-05	0.00497062	synonymous-codon, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416943	ATCTGTCAAAGCTGG[A/G]ACCAAGGAACTTTGG	5252
rs759888026	snp	G/T			intron-variant	PHF1	GRCh38.p7	6:33412982	TAACCTTTGCAGGCA[G/T]AAGATGGTTTAAATG	5252
rs760038186	snp	C/T	1.65622e-05	0.00287764	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412307	CTGGTGCCTCCTCAC[C/T]TTGGGACCCAGCTTC	5252
rs760074942	snp	A/G	1.66352e-05	0.00288398	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416617	GCGTTGAAGTATCGC[A/G]GGGATCTTCATGATG	5252
rs760081649	snp	C/T	1.65048e-05	0.00287265	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413469	GGTATGAAGCTTTCT[C/T]TGCCATATGGACTGA	5252
rs760162635	snp	C/T	0.000107198	0.00732036	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33414998	GGGGTCTCACGTCCC[C/T]TGGGGAAGCGCCGGA	5252
rs760218575	in-del	-/GTG	0.00013083	0.0080869	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409714	CAGATCTGTGTGTGT[-/GTG]GTGTGTGTGTGTGTG	5252
rs760288288	snp	A/G	0.00029679	0.0121781	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416697	ACTCTGTGACCTGGC[A/G]CACCCACTGCAGGTA	5252
rs760505300	snp	A/G	8.78866e-05	0.00662839	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415370	ACAAAATATGCTCCC[A/G]ATTATTCACATCTTC	5252
rs760691835	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33413042	AAGTCCCTTAACCTC[C/T]AGGAGCCTCAGTTCC	5252
rs760700226	snp	C/G	4.94466e-05	0.00497201	intron-variant, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415300	CAGCGGCTACAACTT[C/G]CGGCCCACAGATGCC	5252
rs760706698	snp	A/T	1.64757e-05	0.00287012	intron-variant	PHF1	GRCh38.p7	6:33414463	CTGGCCCCATTTTTC[A/T]TCATTTCTCCCAGCT	5252
rs760717298	in-del	-/GCAGAGGGAGCGGGCTCATCT	1.70075e-05	0.00291607	cds-indel, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415108	GCCCGAGCCCCAGGA[-/GCAGAGGGAGCGGGCTCATCT]GCAGAGGGCACTGCA	5252
rs760739176	snp	A/G			intron-variant	PHF1	GRCh38.p7	6:33414174	CACTCTATATGCCCC[A/G]ACCTCCCACCTCAGG	5252
rs760806385	in-del	-/CT	3.29609e-05	0.00405948	frameshift-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416725	GTACGGAAAGTTCCC[-/CT]GTTCCACAGGCAATG	5252
rs761072121	snp	C/T	1.66477e-05	0.00288506	intron-variant	PHF1	GRCh38.p7	6:33413337	CCTGTGGGAGCCTCC[C/T]ATCCACAGCCTCTCC	5252
rs761180131	snp	C/T	1.64741e-05	0.00286998	intron-variant	PHF1	GRCh38.p7	6:33414024	AAGTGTGTTTGCTCC[C/T]TCTTGCCCATGTCCA	5252
rs761247075	snp	C/T	8.75638e-05	0.00661621	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415077	AGCTGGGGCCACCCT[C/T]AGCAGTGCGCAATCA	5252
rs761268636	snp	A/G	0.000148447	0.00861404	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413250	CTGGAGAGGGAGAGG[A/G]CACATCCTGGGTATG	5252
rs761270949	snp	C/G	0.00277445	0.037142	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409721	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs761460634	snp	C/G	1.66432e-05	0.00288467	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33413742	CCCCCTCAGGTGGAA[C/G]CTGAAAATGCTGCAG	5252
rs761484782	snp	A/G	1.64757e-05	0.00287012	intron-variant	PHF1	GRCh38.p7	6:33415183	TGGAGCAAATGGTGG[A/G]GTGTGGGAAGGAGTC	5252
rs761485096	snp	C/G/T	3.71211e-05	0.00430806	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416136	CCCATTCACACACAC[C/G/T]GGCACTTTCATACCC	5252
rs761582706	in-del	-/C			intron-variant	PHF1	GRCh38.p7	6:33413959	TACCTCACCTGTTTG[-/C]CCCGTCCTTGCTTGT	5252
rs761642211	snp	A/C	1.64746e-05	0.00287002	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412587	GGAAAGACATTAGCC[A/C]TGGTAAGACTCTAGA	5252
rs761678788	snp	A/G	1.64955e-05	0.00287184	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416794	ACAAAATAGGTGGGT[A/G]GGGGAAGGGGATCAC	5252
rs761725434	snp	G/T	1.64773e-05	0.00287026	intron-variant, missense, nc-transcript-variant, utr-variant-3-prime	PHF1	GRCh38.p7	6:33415287	GTTACCAGGGCAGCA[G/T]CGGCTACAACTTCCG	5252
rs761736632	snp	A/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416412	GATCCCGGACTCTGT[A/G]TGATTGAAATAAAGA	5252
rs761828870	snp	A/G			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411240	CGGCAGGAGGCGCTG[A/G]TGGGGGGCAGGGAGC	5252
rs761860568	snp	A/C	1.72487e-05	0.00293667	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415826	TCACCCCTGGAACTT[A/C]ACATTGGTTTCCCCA	5252
rs761910524	snp	A/G			intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415371	CAAAATATGCTCCCA[A/G]TTATTCACATCTTCT	5252
rs761925397	snp	C/G	1.64781e-05	0.00287033	synonymous-codon, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415657	ACCTCTGGGGACAGT[C/G]GACCCCCAGACAGGT	5252
rs761977834	in-del	-/TGTGGG	0.000183036	0.00956475	intron-variant	PHF1	GRCh38.p7	6:33413324	CCCTGTTACCCTTCC[-/TGTGGG]AGCCTCCCATCCACA	5252
rs762015377	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414291	CAGTGTTTGCTGTAA[A/G]AAGAAATACTTTGAT	5252
rs762136379	snp	A/G	1.64882e-05	0.00287121	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413240	GCTCCAGCCCCTGGA[A/G]AGGGAGAGGGCACAT	5252
rs762138976	in-del	-/AGATGTAGCGGAAAGGGGAAGAGAAGAAATCACTGCTCCCCTGGCCCC	1.64789e-05	0.0028704	intron-variant	PHF1	GRCh38.p7	6:33414407	TGGGATGGGACAGGG[lengthTooLong]AGATGTAGCGGAAAG	5252
rs762186487	snp	C/T	1.67349e-05	0.0028926	intron-variant	PHF1	GRCh38.p7	6:33412833	GTCCAGCTTGCTCTT[C/T]CCTCCAGGATGGTCT	5252
rs762229233	snp	A/G	3.48517e-05	0.00417428	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33414979	AGGGCAGGGCCCTGG[A/G]GGAGGGGTCTCACGT	5252
rs762406471	snp	A/G	1.64751e-05	0.00287007	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409608	TGTTGTATTGGTTAC[A/G]CTGCAAACTTTTATC	5252
rs762414042	snp	C/T	1.65269e-05	0.00287457	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413511	TGGGATGCTGGACAT[C/T]TGAGCAACCGACAGC	5252
rs762423401	snp	A/G/T	3.33063e-05	0.00408072	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416615	AGGCGTTGAAGTATC[A/G/T]CGGGGATCTTCATGA	5252
rs762501958	snp	C/T	1.67652e-05	0.00289522	intron-variant	PHF1	GRCh38.p7	6:33413720	TGGAGGCCAGAAGTC[C/T]TGTGTTCCCCCTCAG	5252
rs762622672	snp	C/T	1.64811e-05	0.00287059	synonymous-codon, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416725	GTACGGAAAGTTCCC[C/T]TGTTCCACAGGCAAT	5252
rs762794632	snp	C/T	1.6473e-05	0.00286988	intron-variant	PHF1	GRCh38.p7	6:33412451	CCTCTGACCTTCTTC[C/T]TAGTTCCCTTATCTA	5252
rs762806808	snp	C/T	4.9436e-05	0.00497148	intron-variant	PHF1	GRCh38.p7	6:33414446	AAGAAATCACTGCTC[C/T]CCTGGCCCCATTTTT	5252
rs762874159	snp	C/T	4.94531e-05	0.00497234	splice-acceptor-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416778	AAGGGTGCACAGAAC[C/T]ACAAAATAGGTGGGT	5252
rs762877268	in-del	-/T	1.67179e-05	0.00289114	intron-variant	PHF1	GRCh38.p7	6:33412825	CCTGAATGGTCCAGC[-/T]TGCTCTTCCCTCCAG	5252
rs762993282	snp	C/T	0.000164951	0.00908011	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412351	TCTGGCCCCAGGCCT[C/T]GGCTTTGGGAGGGTC	5252
rs763045540	snp	A/G	0.000148406	0.00861283	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413207	GCAGCTTATCACCAG[A/G]ACTGCCATGTTCCCA	5252
rs763077280	snp	A/G	1.66488e-05	0.00288515	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412788	GCTGTGAGAAGTGTC[A/G]CCATGGTGAGAGGGC	5252
rs763179268	snp	C/G	1.81609e-05	0.00301332	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415382	CCCAATTATTCACAT[C/G]TTCTGGACTTTATCA	5252
rs763272948	snp	A/T	1.68063e-05	0.00289877	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414825	GGAGATGGAGCACTC[A/T]CCAGGTCACTGGTCC	5252
rs763294563	in-del	-/GTGTGTGTGTG	1.80984e-05	0.00300813	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409725	TGTGTGTGTGTGTGT[-/GTGTGTGTGTG]TGTGTGTGTGTGTGT	5252
rs763366781	snp	C/T	1.8493e-05	0.00304075	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416122	CCTCTGCCCAGCTCC[C/T]CATTCACACACACCG	5252
rs763423148	snp	A/C/G	0.000165322	0.00909055	stop-lost, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416651	AGGAACAGGGCTCAT[A/C/G]ATGGCAGGACTGTGA	5252
rs763500559	snp	C/G	0.0219515	0.10244	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409711	GATCCAGATCTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs763565150	snp	A/G	1.65822e-05	0.00287938	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415978	TGGGACTGGGGGAGG[A/G]GTCCGAGGTGGGGTT	5252
rs763651644	snp	A/T	1.64746e-05	0.00287002	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409610	TTGTATTGGTTACGC[A/T]GCAAACTTTTATCCT	5252
rs763689278	snp	A/G	1.64768e-05	0.00287021	intron-variant	PHF1	GRCh38.p7	6:33415167	AGCAGGGGGAACCCG[A/G]TGGAGCAAATGGTGG	5252
rs763779171	snp	A/G	1.65288e-05	0.00287474	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413518	CTGGACATCTGAGCA[A/G]CCGACAGCAGAGTTA	5252
rs763802524	snp	A/C	1.64904e-05	0.00287139	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416786	ACAGAACTACAAAAT[A/C]GGTGGGTGGGGGAAG	5252
rs764036806	snp	A/G	1.64762e-05	0.00287016	intron-variant	PHF1	GRCh38.p7	6:33414456	TGCTCCCCTGGCCCC[A/G]TTTTTCTTCATTTCT	5252
rs764053763	snp	A/G	3.29859e-05	0.00406102	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412352	CTGGCCCCAGGCCTC[A/G]GCTTTGGGAGGGTCA	5252
rs764113456	snp	A/G	1.64727e-05	0.00286986	intron-variant	PHF1	GRCh38.p7	6:33412454	CTGACCTTCTTCCTA[A/G]TTCCCTTATCTAATT	5252
rs764138453	snp	A/G	1.648e-05	0.0028705	stop-gained, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416727	ACGGAAAGTTCCCCT[A/G]TTCCACAGGCAATGC	5252
rs764225501	in-del	-/G	3.48002e-05	0.00417119	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409729	TGTGTGTGTGTGTGT[-/G]TGTGTGTGTGTGTGT	5252
rs764305936	snp	A/G	1.66946e-05	0.00288912	intron-variant	PHF1	GRCh38.p7	6:33412815	GGGCAGGTCACCTGA[A/G]TGGTCCAGCTTGCTC	5252
rs764365700	snp	A/G	3.29984e-05	0.00406179	intron-variant	PHF1	GRCh38.p7	6:33412648	AACCTGGCCTAGAGG[A/G]GCAGAAAGAGACTTA	5252
rs764386943	in-del	-/CA	0.00023121	0.0107495	intron-variant	PHF1	GRCh38.p7	6:33413152	TGTCCCAATACCAAG[-/CA]CACACACAGGTATGC	5252
rs764422208	snp	C/T	3.30229e-05	0.0040633	intron-variant, missense, nc-transcript-variant, synonymous-codon, downstream-variant-500B	PHF1	GRCh38.p7	6:33415316	CGGCCCACAGATGCC[C/T]GCTGCCTGCCCAGGT	5252
rs764447410	snp	C/G	0.0160622	0.0881652	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409715	CAGATCTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs764518448	snp	C/G	1.7002e-05	0.0029156	intron-variant	PHF1	GRCh38.p7	6:33414840	ACCAGGTCACTGGTC[C/G]AGGGGGGATGGGGGA	5252
rs764644569	snp	A/G	1.65822e-05	0.00287938	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415991	GGAGTCCGAGGTGGG[A/G]TTGGTTACCTGTCCC	5252
rs764788552	snp	A/C	1.65321e-05	0.00287502	intron-variant	PHF1	GRCh38.p7	6:33413387	ACCCCTCTGAAGCCA[A/C]CCACCTGTCCTGTCT	5252
rs764819983	snp	C/G	7.71218e-05	0.00620926	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415017	GGAAGCGCCGGAGGC[C/G]GGAGCCAGAGCCCCT	5252
rs764905868	snp	A/T	1.89752e-05	0.00308013	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415088	CCCTCAGCAGTGCGC[A/T]ATCAGCCCGAGCCCC	5252
rs765087759	in-del	-/TGTGTGTGTGT	2.27656e-05	0.00337376	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409718	ATCTGTGTGTGTGTG[-/TGTGTGTGTGT]GTGTGTGTGTGTGTG	5252
rs765098175	snp	A/C	1.65029e-05	0.00287248	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412343	CTCCCACCTCTGGCC[A/C]CAGGCCTCGGCTTTG	5252
rs765206511	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414074	CTGTGTGTGTCGCGG[A/G]GGCCCTGAGAAAGTC	5252
rs765292759	snp	C/T	1.64735e-05	0.00286993	intron-variant	PHF1	GRCh38.p7	6:33414238	TGAAAACTTTGTTTT[C/T]CCAGGGTGGATGTGG	5252
rs765346344	snp	C/T			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411248	GGCGCTGGTGGGGGG[C/T]AGGGAGCCGGGGGTC	5252
rs765378788	snp	C/T	1.64727e-05	0.00286986	intron-variant	PHF1	GRCh38.p7	6:33412498	CATCCTGTTTGCTCA[C/T]CCATTCCAGGTGGAC	5252
rs765410362	snp	A/G/T	3.29469e-05	0.00405864	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416944	TCTGTCAAAGCTGGG[A/G/T]CCAAGGAACTTTGGG	5252
rs765602224	in-del	-/TC	0.000164832	0.00907682	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415678	CCAGACAGGTGAGAT[-/TC]TGTCTTCTATTACCA	5252
rs765615074	snp	C/T	1.65111e-05	0.0028732	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416806	GGTGGGGGAAGGGGA[C/T]CACTCAAAGATTTAC	5252
rs765629909	snp	C/G	4.98227e-05	0.00499088	utr-variant-3-prime, missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415961	TGCCGTAGTTTGTCT[C/G]CTGGGACTGGGGGAG	5252
rs765697964	snp	G/T	1.64754e-05	0.00287009	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409604	AAAATGTTGTATTGG[G/T]TACGCTGCAAACTTT	5252
rs765890101	snp	C/G	6.8171e-05	0.00583788	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412251	TTTTCTGGCTAGGCC[C/G]CCCCAGGATGCAATG	5252
rs765907742	snp	C/T	1.71023e-05	0.00292419	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415007	CGTCCCCTGGGGAAG[C/T]GCCGGAGGCCGGAGC	5252
rs765992367	snp	A/G	1.66106e-05	0.00288184	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414737	CAGTTTCATTTCAGG[A/G]AGAGAGATTAAGAAG	5252
rs765997615	snp	A/G	1.7195e-05	0.0029321	intron-variant	PHF1	GRCh38.p7	6:33414854	CCAGGGGGGATGGGG[A/G]AAATTCTCAGGGTGT	5252
rs766106995	snp	A/G	1.65732e-05	0.00287859	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416632	GGGGATCTTCATGAT[A/G]AGCAGGAACAGGGCT	5252
rs766193284	snp	C/G/T	0.00102821	0.0226509	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409727	TGTGTGTGTGTGTGT[C/G/T]TGTGTGTGTGTGTGT	5252
rs766364303	snp	C/T	1.6473e-05	0.00286988	intron-variant	PHF1	GRCh38.p7	6:33412486	TGGTTCCCATTTCAT[C/T]CTGTTTGCTCACCCA	5252
rs766368568	snp	A/C	1.64841e-05	0.00287085	intron-variant, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415301	AGCGGCTACAACTTC[A/C]GGCCCACAGATGCCC	5252
rs766376296	in-del	-/TAGG	0.000131891	0.00811962	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416785	CACAGAACTACAAAA[-/TAGG]TGGGTGGGGGAAGGG	5252
rs766379296	snp	G/T	1.65811e-05	0.00287929	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33413824	AAGCCCCTCCTCTAT[G/T]GGGACAGGTGAGACC	5252
rs766458873	snp	A/T	1.78086e-05	0.00298396	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415376	TATGCTCCCAATTAT[A/T]CACATCTTCTGGACT	5252
rs766533022	snp	C/T			intron-variant	KIFC1	GRCh38.p7	6:33408562	TATGAAGACATTTGC[C/T]TTGCCATCTACTTGG	5252
rs766716014	snp	A/G/T	1.65211e-05	0.00287407	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415541	TTCCCAGGGGGAGAA[A/G/T]GTCCTGTTCCCCTGC	5252
rs766728612	snp	A/G			synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414095	TGAGAAAGTCCGGAG[A/G]CTACAGCTTCGCTGG	5252
rs766736003	snp	C/T	0.000131965	0.0081219	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415709	AGTGATGCTCTTCTT[C/T]CCCTCTATGTGCTCA	5252
rs766835712	in-del	-/A	4.96676e-05	0.00498311	intron-variant	PHF1	GRCh38.p7	6:33413570	GGAGTGAGTAATGAG[-/A]GGGGAGCAGACTGTG	5252
rs766898405	in-del	-/TGG	1.64754e-05	0.00287009	intron-variant	PHF1	GRCh38.p7	6:33415177	ACCCGATGGAGCAAA[-/TGG]TGGGGTGTGGGAAGG	5252
rs766934907	snp	C/G	1.65061e-05	0.00287277	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413256	AGGGAGAGGGCACAT[C/G]CTGGGTATGCCGCCA	5252
rs766981651	snp	A/C	1.7105e-05	0.00292441	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412244	CCATTTCTTTTCTGG[A/C]TAGGCCCCCCCAGGA	5252
rs767087913	snp	A/C	6.58913e-05	0.00573945	intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409630	ACTTTTATCCTGTCT[A/C]ACCCCCTGCCCCCAG	5252
rs767179478	snp	C/T	1.85081e-05	0.00304199	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409722	GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG	5252
rs767342191	snp	A/G	1.65542e-05	0.00287695	intron-variant	PHF1	GRCh38.p7	6:33413565	CCTGGGGAGTGAGTA[A/G]TGAGAGGGGAGCAGA	5252
rs767431959	snp	C/G	1.64749e-05	0.00287005	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412589	AAAGACATTAGCCCT[C/G]GTAAGACTCTAGAGA	5252
rs767446720	in-del	-/G	3.59971e-05	0.00424232	intron-variant	PHF1	GRCh38.p7	6:33414876	CAGGGTGTTAGTCCT[-/G]GGGGGGTATATGTAT	5252
rs767493691	snp	A/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414314	ACTTTGATTTTGATC[A/G]TGAGATCCTCCCCTT	5252
rs767540533	snp	G/T	1.64754e-05	0.00287009	intron-variant	PHF1	GRCh38.p7	6:33415184	GGAGCAAATGGTGGG[G/T]TGTGGGAAGGAGTCA	5252
rs767638497	in-del	-/AC	0.000183103	0.0095665	intron-variant	PHF1	GRCh38.p7	6:33413329	TACCCTTCCTGTGGG[-/AC]AGCCTCCCATCCACA	5252
rs767675090	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33413012	GCATCCTTTTCTAAC[C/T]ATATGACCTCGGACA	5252
rs767685893	snp	C/T	1.64792e-05	0.00287042	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415661	CTGGGGACAGTGGAC[C/T]CCCAGACAGGTGAGA	5252
rs767764780	snp	C/T			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411365	CTGGGGAGTAGAGAC[C/T]GGGACTGGGACACGC	5252
rs767831440	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414105	CGGAGACTACAGCTT[C/T]GCTGGTGAGCTGGAT	5252
rs767976185	snp	C/T			synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414324	TGATCGTGAGATCCT[C/T]CCCTTCACTTCTGAG	5252
rs768038392	snp	G/T	1.70064e-05	0.00291597	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415349	GTGCTCCTCTGCCCC[G/T]CCCCCACAAAATATG	5252
rs768092213	snp	G/T	1.70831e-05	0.00292254	intron-variant	PHF1	GRCh38.p7	6:33414847	CACTGGTCCAGGGGG[G/T]ATGGGGGAAATTCTC	5252
rs768144708	snp	C/T	1.67153e-05	0.00289091	intron-variant	PHF1	GRCh38.p7	6:33413730	AAGTCCTGTGTTCCC[C/T]CTCAGGTGGAACCTG	5252
rs768179996	snp	G/T	0.00012851	0.00801489	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33414984	AGGGCCCTGGGGGAG[G/T]GGTCTCACGTCCCCT	5252
rs768184511	snp	C/G	1.68216e-05	0.00290009	intron-variant	PHF1	GRCh38.p7	6:33412844	TCTTCCCTCCAGGAT[C/G]GTCTCTATATCACCT	5252
rs768303839	snp	G/T	1.64749e-05	0.00287005	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412584	TATGGAAAGACATTA[G/T]CCCTGGTAAGACTCT	5252
rs768307272	snp	A/G	4.94197e-05	0.00497066	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416910	ACCCCATCCATCTCA[A/G]AGTTCTCACCGAACA	5252
rs768341411	snp	C/T	1.64749e-05	0.00287005	intron-variant, synonymous-codon, nc-transcript-variant, missense, utr-variant-3-prime	PHF1	GRCh38.p7	6:33415273	CAGCCCTAACCAGAG[C/T]TACCAGGGCAGCAGC	5252
rs768477008	snp	C/T	1.66732e-05	0.00288727	intron-variant	PHF1	GRCh38.p7	6:33414720	CATTTCTCTTCTTGC[C/T]CCAGTTTCATTTCAG	5252
rs768508950	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414542	TAACAGCCACAAGGA[C/T]CGGTGAGTTGGAGGG	5252
rs768512627	in-del	-/TG	1.67911e-05	0.00289746	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416589	GGCCCAGTCATCACC[-/TG]GAAGTCAGAAGGCGT	5252
rs768637374	in-del	-/GTA	1.64762e-05	0.00287016	intron-variant	PHF1	GRCh38.p7	6:33414374	TGGGGGAGGTAAGGG[-/GTA]GTGCAGTTTTGGGGG	5252
rs768704721	snp	C/T	0.000141613	0.00841347	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33414974	CCTTCAGGGCAGGGC[C/T]CTGGGGGAGGGGTCT	5252
rs768716810	snp	C/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416192	GGATGTACCTGGAGA[C/G]ATAGGGGGTAGTTCT	5252
rs768780021	snp	C/T	1.6486e-05	0.00287102	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413226	GCCATGTTCCCAGGG[C/T]TCCAGCCCCTGGAGA	5252
rs769087516	snp	C/T	1.64746e-05	0.00287002	intron-variant	PHF1	GRCh38.p7	6:33414017	CCTGTGTAAGTGTGT[C/T]TGCTCCCTCTTGCCC	5252
rs769140145	snp	A/G	1.66696e-05	0.00288696	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416612	AGAAGGCGTTGAAGT[A/G]TCGCGGGGATCTTCA	5252
rs769277962	snp	C/G	1.65021e-05	0.00287241	intron-variant	PHF1	GRCh38.p7	6:33415156	GCAGGTACTGGAGCA[C/G]GGGGAACCCGATGGA	5252
rs769279641	snp	A/C	1.64768e-05	0.00287021	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416890	CCCACACAGTACACA[A/C]CCTCACCCCATCCAT	5252
rs769430376	in-del	-/A	1.65026e-05	0.00287246	intron-variant	PHF1	GRCh38.p7	6:33412662	GGCAGAAAGAGACTT[-/A]AAAGGCAGGCCCTGT	5252
rs769474314	snp	C/G	1.64846e-05	0.0028709	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416772	CTTCGTAAGGGTGCA[C/G]AGAACTACAAAATAG	5252
rs769506496	snp	C/T	1.64762e-05	0.00287016	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414534	TCTGCTCTTAACAGC[C/T]ACAAGGACCGGTGAG	5252
rs769598670	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412549	GGTCCAGTTTGAGGA[C/T]GATTCGCAGTTTCTG	5252
rs769661737	snp	A/C	6.90346e-05	0.00587473	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415815	CTCTCCCTAGGTCAC[A/C]CCTGGAACTTCACAT	5252
rs769711852	snp	C/T	1.6476e-05	0.00287014	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415643	CCAGCACCGCAGGGA[C/T]CTCTGGGGACAGTGG	5252
rs769735340	in-del	-/TGAGGTGGGTGGATCATGAGGTCAGGAGT	1.64749e-05	0.00287005	intron-variant	PHF1	GRCh38.p7	6:33414200	CAGGACTCCCCTGGC[lengthTooLong]TCTTAAAATGCCTCT	5252
rs769836466	snp	C/T	1.66261e-05	0.00288319	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412771	TGGGAACCGGCTGGT[C/T]AGCTGTGAGAAGTGT	5252
rs769849330	in-del	-/TGTGTGTGTG			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409708	ACGGATCCAGATCTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT	5252
rs769890770	snp	C/T	3.42988e-05	0.00414104	intron-variant	PHF1	GRCh38.p7	6:33414917	AGGTCTTGGGGGTGT[C/T]CGGGAGGGGGCTGGG	5252
rs769924134	snp	A/G	1.65048e-05	0.00287265	intron-variant	PHF1	GRCh38.p7	6:33413183	AATAAGTGGTCTACT[A/G]TTATCACTGCAGCTT	5252
rs769938402	snp	C/G	1.66305e-05	0.00288357	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414795	CGGATGCCTCCCCCT[C/G]TGGAGCCCCCTACTG	5252
rs770084680	snp	A/G	0.00021767	0.0104301	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416597	CATCACCTGGAAGTC[A/G]GAAGGCGTTGAAGTA	5252
rs770110682	snp	C/T	5.14505e-05	0.00507174	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412224	CATTCATAACCTTCT[C/T]CTCCCCATTTCTTTT	5252
rs770216568	snp	A/C	4.94214e-05	0.00497074	intron-variant, missense, nc-transcript-variant, utr-variant-3-prime	PHF1	GRCh38.p7	6:33415250	GCCTCAGTGTCTCCA[A/C]CATCCCCCAGCCCTA	5252
rs770329341	snp	C/T	3.29457e-05	0.00405854	intron-variant	PHF1	GRCh38.p7	6:33412437	GGTAAGACCTTCTAC[C/T]TCTGACCTTCTTCCT	5252
rs770339717	snp	A/C	1.64879e-05	0.00287118	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416700	CTGTGACCTGGCGCA[A/C]CCACTGCAGGTACGG	5252
rs770368799	snp	C/G	1.68244e-05	0.00290033	intron-variant	PHF1	GRCh38.p7	6:33413698	CAGTTATGGGGAAGG[C/G]GGTTTCTGGAGGCCA	5252
rs770498402	in-del	-/C	0.000611086	0.0174691	frameshift-variant, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412272	GATGCAATGGCGCAG[-/C]CCCCCCCGGCTGAGC	5252
rs770529391	snp	A/C			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409043	CGTGGTGGCGGGCGC[A/C]TGTAGTCTCAGCTAC	5252
rs770727153	snp	C/G/T	3.29702e-05	0.00406008	intron-variant	PHF1	GRCh38.p7	6:33414416	GACAGGGAGATGTAG[C/G/T]GGAAAGGGGAAGAGA	5252
rs770833118	snp	A/G	1.64754e-05	0.00287009	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415631	TCCACCCTTCTGCCA[A/G]CACCGCAGGGACCTC	5252
rs770834046	in-del	-/G	4.7408e-05	0.00486844	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409716	GATCTGTGTGTGTGT[-/G]GTGTGTGTGTGTGTG	5252
rs770950218	in-del	-/T	4.94197e-05	0.00497066	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416908	CACCCCATCCATCTC[-/T]AAAGTTCTCACCGAA	5252
rs770984857	snp	C/T	1.73881e-05	0.00294852	downstream-variant-500B, utr-variant-3-prime, synonymous-codon, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416056	ACGGCCTGATGGCTC[C/T]GTGCAGTACCTGGTT	5252
rs771065793	snp	C/T			intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415475	ACTAGTGTCTGGTAG[C/T]CAGTATTCTGGGGAA	5252
rs771282153	snp	A/G	2.05122e-05	0.00320245	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415081	GGGGCCACCCTCAGC[A/G]GTGCGCAATCAGCCC	5252
rs771407202	snp	A/G	3.2963e-05	0.00405961	synonymous-codon, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416761	TACCTCGGCCACTTC[A/G]TAAGGGTGCACAGAA	5252
rs771460024	snp	A/C	1.64727e-05	0.00286986	intron-variant	PHF1	GRCh38.p7	6:33414148	CAGTGTAACTCCACA[A/C]CACAGTATTTCACTC	5252
rs771512484	in-del	-/GTGTG	0.0002674	0.0115598	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409712	TCCAGATCTGTGTGT[-/GTGTG]GTGTGTGTGTGTGTG	5252
rs771629046	snp	C/T	1.6577e-05	0.00287893	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412301	GCCGCTCTGGTGCCT[C/T]CTCACTTTGGGACCC	5252
rs771682288	in-del	-/T	0.000188535	0.00970732	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412236	TCTCCTCCCCATTTC[-/T]TTTCTGGCTAGGCCC	5252
rs771789201	snp	C/T	1.64738e-05	0.00286995	intron-variant	PHF1	GRCh38.p7	6:33414028	GTGTTTGCTCCCTCT[C/T]GCCCATGTCCAGGTT	5252
rs772316615	in-del	-/CT	1.64985e-05	0.0028721	frameshift-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416683	AGAGTCAGAAACTGA[-/CT]CTGTGACCTGGCGCA	5252
rs772352148	snp	A/G	1.66713e-05	0.0028871	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415119	AGGAGCAGAGGGAGC[A/G]GGCTCATCTGCAGAG	5252
rs772354146	snp	C/T	1.66251e-05	0.0028831	intron-variant	PHF1	GRCh38.p7	6:33413320	ACTTCCCTGTTACCC[C/T]TCCTGTGGGAGCCTC	5252
rs772445178	snp	C/T	6.59946e-05	0.00574395	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413421	CAGAGGGGAGGTGCC[C/T]TGAAGAAGGGCCCCT	5252
rs772553079	snp	C/T	2.2458e-05	0.0033509	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415075	GGAGCTGGGGCCACC[C/T]TCAGCAGTGCGCAAT	5252
rs772678086	snp	C/T	1.64933e-05	0.00287165	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416691	AAACTGACTCTGTGA[C/T]CTGGCGCACCCACTG	5252
rs772709521	snp	G/T	1.64735e-05	0.00286993	intron-variant	PHF1	GRCh38.p7	6:33414035	CTCCCTCTTGCCCAT[G/T]TCCAGGTTCTATGAA	5252
rs772739997	in-del	-/T	2.87208e-05	0.0037894	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409714	CCAGATCTGTGTGTG[-/T]GTGTGTGTGTGTGTG	5252
rs772916682	snp	A/C/T	3.41415e-05	0.00413156	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412250	CTTTTCTGGCTAGGC[A/C/T]CCCCCAGGATGCAAT	5252
rs772973458	snp	A/C	1.64735e-05	0.00286993	intron-variant	PHF1	GRCh38.p7	6:33414159	CACACCACAGTATTT[A/C]ACTCTATATGCCCCA	5252
rs773162434	snp	A/C	1.73824e-05	0.00294803	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415365	CCCCCACAAAATATG[A/C]TCCCAATTATTCACA	5252
rs773189516	snp	A/T	1.64762e-05	0.00287016	intron-variant	PHF1	GRCh38.p7	6:33414458	CTCCCCTGGCCCCAT[A/T]TTTCTTCATTTCTCC	5252
rs773209180	snp	G/T	1.72371e-05	0.00293568	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415831	CCTGGAACTTCACAT[G/T]GGTTTCCCCACAGAC	5252
rs773273132	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416940	AAAATCTGTCAAAGC[C/T]GGGACCAAGGAACTT	5252
rs773372494	in-del	-/A	0.000120795	0.00777064	frameshift-variant, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33414990	TGGGGGAGGGGTCTC[-/A]ACGTCCCCTGGGGAA	5252
rs773526973	snp	G/T	1.65018e-05	0.00287239	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413439	AAGAAGGGCCCCTAT[G/T]CCCGGGCCATGCTGG	5252
rs773698135	snp	C/G			utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416580	TTTATTGGGGGCCCA[C/G]TCATCACCTGGAAGT	5252
rs773725188	snp	C/G	1.66402e-05	0.00288441	intron-variant	PHF1	GRCh38.p7	6:33413322	TTCCCTGTTACCCTT[C/G]CTGTGGGAGCCTCCC	5252
rs773835457	snp	C/T	1.72779e-05	0.00293916	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33414992	GGGGGAGGGGTCTCA[C/T]GTCCCCTGGGGAAGC	5252
rs773853554	snp	C/G	0.0153301	0.0861977	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409719	TCTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs773856487	snp	C/T	1.64773e-05	0.00287026	intron-variant, synonymous-codon, nc-transcript-variant, missense, utr-variant-3-prime	PHF1	GRCh38.p7	6:33415285	GAGTTACCAGGGCAG[C/T]AGCGGCTACAACTTC	5252
rs773923547	snp	C/T	1.64928e-05	0.00287161	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415076	GAGCTGGGGCCACCC[C/T]CAGCAGTGCGCAATC	5252
rs774030157	snp	C/T	1.65578e-05	0.00287726	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412731	AACTCCTCTGTTGTG[C/T]CTGTCGCTCTGAGAC	5252
rs774059224	snp	C/T	1.66983e-05	0.00288944	intron-variant	PHF1	GRCh38.p7	6:33413733	TCCTGTGTTCCCCCT[C/T]AGGTGGAACCTGAAA	5252
rs774132381	snp	C/T	1.6473e-05	0.00286988	intron-variant	PHF1	GRCh38.p7	6:33412459	CTTCTTCCTAGTTCC[C/T]TTATCTAATTCTGGT	5252
rs774138173	snp	G/T	1.64912e-05	0.00287147	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416792	CTACAAAATAGGTGG[G/T]TGGGGGAAGGGGATC	5252
rs774309559	in-del	-/GTT	1.67312e-05	0.00289229	cds-indel, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416604	TGGAAGTCAGAAGGC[-/GTT]GAAGTATCGCGGGGA	5252
rs774315100	snp	G/T	3.29598e-05	0.00405941	intron-variant	PHF1	GRCh38.p7	6:33414551	CAAGGACCGGTGAGT[G/T]GGAGGGAAGAGGAGG	5252
rs774394651	snp	C/T	8.56876e-05	0.00654496	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412240	CTCCCCATTTCTTTT[C/T]TGGCTAGGCCCCCCC	5252
rs774413269	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412586	TGGAAAGACATTAGC[C/T]CTGGTAAGACTCTAG	5252
rs774504365	in-del	-/TG	9.89674e-05	0.00703377	frameshift-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416686	GTCAGAAACTGACTC[-/TG]TGACCTGGCGCACCC	5252
rs774607210	snp	C/T	1.64852e-05	0.00287094	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413228	CATGTTCCCAGGGCT[C/T]CAGCCCCTGGAGAGG	5252
rs774683950	snp	A/G	2.64645e-05	0.00363752	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415067	AAAGTGGAGGAGCTG[A/G]GGCCACCCTCAGCAG	5252
rs774699588	snp	C/T			intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415482	TCTGGTAGCCAGTAT[C/T]CTGGGGAAGGGAGTC	5252
rs774706003	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33412870	CACCTGTCCTGGCCT[C/T]AGTCCCCAAGCCACT	5252
rs774848248	in-del	-/TGTGTGTGTG			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409724	GTGTGTGTGTGTGTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT	5252
rs774882082	snp	C/T	0.000140637	0.00838444	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33414975	CTTCAGGGCAGGGCC[C/T]TGGGGGAGGGGTCTC	5252
rs774988390	snp	A/G	1.85451e-05	0.00304503	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416134	TCCCCATTCACACAC[A/G]CCGGCACTTTCATAC	5252
rs774999747	snp	C/T	0.000115324	0.00759268	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416892	CACACAGTACACACC[C/T]TCACCCCATCCATCT	5252
rs775075006	snp	A/G	1.6516e-05	0.00287362	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413492	TGGACTGAAGGGGCT[A/G]GACTGGGATGCTGGA	5252
rs775099271	snp	A/G	1.64844e-05	0.00287087	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416775	CGTAAGGGTGCACAG[A/G]ACTACAAAATAGGTG	5252
rs775187176	snp	C/T	1.6492e-05	0.00287154	intron-variant	PHF1	GRCh38.p7	6:33415164	TGGAGCAGGGGGAAC[C/T]CGATGGAGCAAATGG	5252
rs775218685	snp	G/T			intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410082	ACCCCGTCCGTCACA[G/T]CAGGGAGGTGTGCCC	5252
rs775282401	snp	A/G			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409188	ACAACAAAAAAAAGA[A/G]CCTCCTTCAGATTGG	5252
rs775335564	in-del	-/T	1.64749e-05	0.00287005	intron-variant	PHF1	GRCh38.p7	6:33414202	GGACTCCCCTGGCTC[-/T]TTAAAATGCCTCTGT	5252
rs775382376	in-del	-/G	1.671e-05	0.00289045	intron-variant	PHF1	GRCh38.p7	6:33412822	CACCTGAATGGTCCA[-/G]GCTTGCTCTTCCCTC	5252
rs775426396	snp	C/T	6.58903e-05	0.00573941	intron-variant	PHF1	GRCh38.p7	6:33412448	CTACCTCTGACCTTC[C/T]TCCTAGTTCCCTTAT	5252
rs775478494	snp	C/T	1.7251e-05	0.00293687	missense, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415824	GGTCACCCCTGGAAC[C/T]TCACATTGGTTTCCC	5252
rs775547414	snp	A/G	1.64993e-05	0.00287218	intron-variant	PHF1	GRCh38.p7	6:33413192	TCTACTATTATCACT[A/G]CAGCTTATCACCAGG	5252
rs775549078	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414249	TTTTTCCAGGGTGGA[C/T]GTGGCCCATCTTGTC	5252
rs775566380	snp	G/T	1.648e-05	0.0028705	intron-variant	PHF1	GRCh38.p7	6:33414442	AGAGAAGAAATCACT[G/T]CTCCCCTGGCCCCAT	5252
rs775587165	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33414168	GTATTTCACTCTATA[C/T]GCCCCAACCTCCCAC	5252
rs775629901	snp	C/G	9.87996e-05	0.0070278	intron-variant	PHF1	GRCh38.p7	6:33414923	TGGGGGTGTCCGGGA[C/G]GGGGCTGGGGGGATA	5252
rs775646492	snp	A/G	1.65875e-05	0.00287984	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415972	GTCTCCTGGGACTGG[A/G]GGAGGAGTCCGAGGT	5252
rs775759898	snp	C/T	1.66452e-05	0.00288484	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412787	AGCTGTGAGAAGTGT[C/T]GCCATGGTGAGAGGG	5252
rs775832631	snp	C/T	1.68114e-05	0.00289921	intron-variant	PHF1	GRCh38.p7	6:33413711	GGGGGTTTCTGGAGG[C/T]CAGAAGTCCTGTGTT	5252
rs775934235	snp	C/T	1.71481e-05	0.0029281	intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412225	ATTCATAACCTTCTC[C/T]TCCCCATTTCTTTTC	5252
rs776048307	snp	A/G	1.64838e-05	0.00287083	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416708	TGGCGCACCCACTGC[A/G]GGTACGGAAAGTTCC	5252
rs776102099	snp	C/T	0.000545135	0.0165006	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412322	TTTGGGACCCAGCTT[C/T]TCCTGCTCCCACCTC	5252
rs776369338	in-del	-/CTT	1.64731e-05	0.00286989	intron-variant	PHF1	GRCh38.p7	6:33412444	CCTTCTACCTCTGAC[-/CTT]CTTCCTAGTTCCCTT	5252
rs776389641	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33412443	ACCTTCTACCTCTGA[C/T]CTTCTTCCTAGTTCC	5252
rs776449354	snp	C/G			intron-variant	PHF1	GRCh38.p7	6:33412610	ACTCTAGAGACCTGA[C/G]ATTGCACATCCCATG	5252
rs776507326	snp	C/T			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416218	GTTCTCCCTACTGCC[C/T]AGGCTGGAATCCAAG	5252
rs776526888	snp	C/T			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409338	ACTATTTTATCTCGG[C/T]TTAAGTGTTTTACAG	5252
rs776578484	snp	A/C	1.64743e-05	0.00287	intron-variant	PHF1	GRCh38.p7	6:33414205	ACTCCCCTGGCTCTT[A/C]AAATGCCTCTGTGGT	5252
rs776690807	in-del	-/TGTGTGT			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409718	ATCTGTGTGTGTGTG[-/TGTGTGT]GTGTGTGTGTGTGTG	5252
rs776697535	snp	C/T	6.58968e-05	0.00573969	intron-variant	PHF1	GRCh38.p7	6:33412605	GTAAGACTCTAGAGA[C/T]CTGAGATTGCACATC	5252
rs776703783	snp	A/G	3.31625e-05	0.00407188	synonymous-codon, nc-transcript-variant, missense	PHF1	GRCh38.p7	6:33414758	GATTAAGAAGAGGAA[A/G]TGTTTGTTTGGTCTC	5252
rs776784098	snp	C/T	1.81698e-05	0.00301406	downstream-variant-500B, utr-variant-3-prime, missense, nc-transcript-variant	CUTA, PHF1	GRCh38.p7	6:33416091	GGGGAGGAGGGGGCA[C/T]CTTCTGAACAGCCTG	5252
rs776904705	snp	A/G	0.000148337	0.00861085	intron-variant	PHF1	GRCh38.p7	6:33414566	TGGAGGGAAGAGGAG[A/G]CAAGGATGAGGCTCG	5252
rs776938881	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	KIFC1, PHF1	GRCh38.p7	6:33410337	CGCTCGCTGCCCATT[A/G]GCTGGCTCTCGGTGG	5252
rs776956807	snp	C/T	1.65102e-05	0.00287312	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409694	AACAGGAAGTGAAGA[C/T]GGATCCAGATCTGTG	5252
rs776968589	snp	C/T	1.65332e-05	0.00287512	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415139	CATCTGCAGAGGGCA[C/T]TGCAGGTACTGGAGC	5252
rs777060378	snp	G/T	1.64988e-05	0.00287213	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413454	GCCCGGGCCATGCTG[G/T]GTATGAAGCTTTCTC	5252
rs777067920	in-del	-/C	1.64751e-05	0.00287007	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416895	CAGTACACACCCTCA[-/C]CCCCATCCATCTCAA	5252
rs777108891	snp	C/T	8.23635e-05	0.00641677	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414332	AGATCCTCCCCTTCA[C/T]TTCTGAGAATTGGGA	5252
rs777152109	snp	C/T	1.64765e-05	0.00287019	intron-variant	PHF1	GRCh38.p7	6:33414380	AGGTAAGGGGTAGTG[C/T]AGTTTTGGGGGTTGG	5252
rs777163492	snp	C/G	1.65471e-05	0.00287633	intron-variant	PHF1	GRCh38.p7	6:33413374	TTTTCCTCTCCCCAC[C/G]CCTCTGAAGCCACCC	5252
rs777399778	in-del	-/CTCT	1.67267e-05	0.0028919	intron-variant	PHF1	GRCh38.p7	6:33413848	TGAGACCAAGGCAGA[-/CTCT]CTAGGAGCCAAGGAT	5252
rs777423175	snp	C/T	1.68168e-05	0.00289967	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415888	GACTGCCTCATCTTC[C/T]TCAGTTTCATCCCCA	5252
rs777625250	snp	A/G	1.70676e-05	0.00292122	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415782	TCTCCATTTCTGCCC[A/G]TTTCTTACAATTGCC	5252
rs777731612	snp	C/T	4.95193e-05	0.00497566	intron-variant	PHF1	GRCh38.p7	6:33413178	TATGCAATAAGTGGT[C/T]TACTATTATCACTGC	5252
rs777818163	snp	C/G	3.295e-05	0.00405881	intron-variant, missense	PHF1	GRCh38.p7	6:33415221	ATCTCTCAGTCCTTT[C/G]CCCCCTCTTCTAGGC	5252
rs777876494	snp	A/T	1.65105e-05	0.00287315	intron-variant	PHF1	GRCh38.p7	6:33415149	GGGCACTGCAGGTAC[A/T]GGAGCAGGGGGAACC	5252
rs777906203	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416612	GAAGGCGTTGAAGTA[-/T]TCGCGGGGATCTTCA	5252
rs777988686	snp	C/G	3.29468e-05	0.00405861	missense, upstream-variant-2KB, utr-variant-3-prime	KIFC1, PHF1	GRCh38.p7	6:33409681	TACTGCTCAGGCCAA[C/G]AGGAAGTGAAGACGG	5252
rs777993011	snp	C/T	3.35065e-05	0.00409293	intron-variant	PHF1	GRCh38.p7	6:33413850	AGACCAAGGCAGACT[C/T]TCTAGGAGCCAAGGA	5252
rs778010252	snp	A/C	3.29679e-05	0.00405991	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416876	CCCAGCAAGTCACAC[A/C]CACACAGTACACACC	5252
rs778061123	snp	C/G			missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414102	GTCCGGAGACTACAG[C/G]TTCGCTGGTGAGCTG	5252
rs778105253	snp	C/G	1.6473e-05	0.00286988	intron-variant	PHF1	GRCh38.p7	6:33412430	TCAAAAAGGTAAGAC[C/G]TTCTACCTCTGACCT	5252
rs778175065	snp	A/G			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33411656	AGGCCAGTATATAAT[A/G]TCCCAGGAGAGCTCT	5252
rs778291856	snp	C/T	3.29468e-05	0.00405861	missense, nc-transcript-variant, synonymous-codon	PHF1	GRCh38.p7	6:33414501	ACCCCCAAAGGAGAA[C/T]GTTCTTCCAGGCTCC	5252
rs778301740	snp	C/T	0.000197834	0.00994373	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415584	CTTTCCCCACTCCAA[C/T]CCCAGCAGCCCCATC	5252
rs778396112	snp	A/G	3.29451e-05	0.00405851	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412510	TCACCCATTCCAGGT[A/G]GACAGTGCTAGGGAG	5252
rs778408444	snp	C/G/T	3.29632e-05	0.00405964	missense, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416760	TTACCTCGGCCACTT[C/G/T]GTAAGGGTGCACAGA	5252
rs778424334	in-del	-/GTGTG	5.16329e-05	0.00508073	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409708	CGGATCCAGATCTGT[-/GTGTG]GTGTGTGTGTGTGTG	5252
rs778556692	snp	A/C			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409159	CGACAGAGCAAGACT[A/C]CGTCTCAACAACAAC	5252
rs778588498	snp	A/T	1.65121e-05	0.00287329	intron-variant	PHF1	GRCh38.p7	6:33413165	AAGCACACACAGGTA[A/T]GCAATAAGTGGTCTA	5252
rs778609043	snp	A/C			missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412556	TTTGAGGATGATTCG[A/C]AGTTTCTGGTTCTAT	5252
rs778773569	snp	C/G	1.66682e-05	0.00288684	intron-variant	PHF1	GRCh38.p7	6:33414721	ATTTCTCTTCTTGCC[C/G]CAGTTTCATTTCAGG	5252
rs778774083	snp	C/T	3.56939e-05	0.00422441	intron-variant	PHF1	GRCh38.p7	6:33414875	CTCAGGGTGTTAGTC[C/T]TGGGGGGTATATGTA	5252
rs778930297	snp	C/G	0.0144147	0.0836634	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409731	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT	5252
rs778946600	snp	C/T			intron-variant, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409633	TTTATCCTGTCTAAC[C/T]CCCTGCCCCCAGGTG	5252
rs779056192	snp	G/T	1.65026e-05	0.00287246	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33413415	TCTCTGCAGAGGGGA[G/T]GTGCCCTGAAGAAGG	5252
rs779140600	snp	A/C	1.64749e-05	0.00287005	intron-variant	PHF1	GRCh38.p7	6:33415206	AAGGAGTCAAGGATT[A/C]TCTCTCAGTCCTTTG	5252
rs779235793	snp	A/G	1.6473e-05	0.00286988	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412421	TGGGTACCATCAAAA[A/G]GGTAAGACCTTCTAC	5252
rs779304979	snp	C/G	3.33095e-05	0.00408089	intron-variant	PHF1	GRCh38.p7	6:33413341	TGGGAGCCTCCCATC[C/G]ACAGCCTCTCCCAAG	5252
rs779338684	snp	A/G	3.3461e-05	0.00409016	missense, synonymous-codon, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415117	CCAGGAGCAGAGGGA[A/G]CGGGCTCATCTGCAG	5252
rs779434314	snp	A/G	1.6504e-05	0.00287258	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415720	TCTTCCCCTCTATGT[A/G]CTCAAGGCTCTTAGT	5252
rs779443869	snp	A/G	3.29527e-05	0.00405898	intron-variant	PHF1	GRCh38.p7	6:33414374	TGGGGGAGGTAAGGG[A/G]TAGTGCAGTTTTGGG	5252
rs779729918	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	PHF1	GRCh38.p7	6:33414535	CTGCTCTTAACAGCC[A/G]CAAGGACCGGTGAGT	5252
rs779807497	snp	A/G	3.31329e-05	0.00407005	intron-variant	PHF1	GRCh38.p7	6:33413583	AGAGGGGAGCAGACT[A/G]TGGAATGAATGATGT	5252
rs779913147	snp	G/T	1.66913e-05	0.00288883	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33416011	TTACCTGTCCCGAGG[G/T]GACCCTGTCCGGGTC	5252
rs780033853	in-del	-/GAT	5.09169e-05	0.00504538	cds-indel, nc-transcript-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415870	AAGTGCCCCCCACTC[-/GAT]GACTGCCTCATCTTC	5252
rs780098538	snp	A/G	1.68298e-05	0.00290079	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412280	TGGCGCAGCCCCCCC[A/G]GCTGAGCCGCTCTGG	5252
rs780106729	snp	G/T	1.6722e-05	0.00289149	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416602	CCTGGAAGTCAGAAG[G/T]CGTTGAAGTATCGCG	5252
rs780198448	snp	A/G	3.62759e-05	0.00425871	synonymous-codon, missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415053	GGAGGCAGAAGGGGA[A/G]AGTGGAGGAGCTGGG	5252
rs780370346	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412398	ATGGACTGATGGGCT[A/G]CTATACTTGGGTACC	5252
rs780480282	in-del	-/G			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409735	TGTGTGTGTGTGTGT[-/G]TGTGTGTGTGTGTGT	5252
rs780511691	snp	C/T	1.68405e-05	0.00290172	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415342	CAGGTCAGTGCTCCT[C/T]TGCCCCTCCCCCACA	5252
rs780576229	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant, utr-variant-5-prime	PHF1	GRCh38.p7	6:33412517	TTCCAGGTGGACAGT[A/G]CTAGGGAGGTGTGTC	5252
rs780599482	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33414006	GGCACAGTTTTCCTG[C/T]GTAAGTGTGTTTGCT	5252
rs780599637	snp	C/T	1.6495e-05	0.0028718	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415574	CAGGTCCTGACTTTC[C/T]CCACTCCAACCCCAG	5252
rs780743710	in-del	-/A	1.70895e-05	0.00292309	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415788	TTCTGCCCATTTCTT[-/A]ACAATTGCCTTCTCT	5252
rs780780759	in-del	-/TG	1.64727e-05	0.00286986	frameshift-variant, nc-transcript-variant	PHF1	GRCh38.p7	6:33414060	TATGAATTTGAATGC[-/TG]TGTGTGTCGCGGGGG	5252
rs780855795	snp	C/G	1.67298e-05	0.00289217	intron-variant	PHF1	GRCh38.p7	6:33414693	CCGTTTTTTACAGCA[C/G]TGACCCTATATCATT	5252
rs780956155	snp	C/T	1.74124e-05	0.00295057	missense, nc-transcript-variant, intron-variant	PHF1	GRCh38.p7	6:33415100	CGCAATCAGCCCGAG[C/T]CCCAGGAGCAGAGGG	5252
rs781042292	snp	A/G	1.65176e-05	0.00287376	intron-variant	PHF1	GRCh38.p7	6:33413399	CCACCCACCTGTCCT[A/G]TCTCTGCAGAGGGGA	5252
rs781071651	snp	A/G	1.65792e-05	0.00287912	intron-variant	PHF1	GRCh38.p7	6:33413299	GATCGCCACCAAGGT[A/G]AAGGCACTTCCCTGT	5252
rs781145600	snp	A/T	1.71217e-05	0.00292584	intron-variant, downstream-variant-500B	PHF1	GRCh38.p7	6:33415792	TGCCCATTTCTTACA[A/T]TTGCCTTCTCTCCCT	5252
rs781188470	snp	C/T			intron-variant	PHF1	GRCh38.p7	6:33413869	AGGAGCCAAGGATGC[C/T]CTCTTTCTTCGTGTT	5252
rs781342305	snp	C/T	1.68213e-05	0.00290006	utr-variant-3-prime, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416578	GATTTATTGGGGGCC[C/T]AGTCATCACCTGGAA	5252
rs781403506	snp	C/T	1.69029e-05	0.00290709	missense, nc-transcript-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412274	ATGCAATGGCGCAGC[C/T]CCCCCGGCTGAGCCG	5252
rs781411234	snp	C/T	3.30671e-05	0.00406602	intron-variant, missense, nc-transcript-variant, synonymous-codon, downstream-variant-500B	PHF1	GRCh38.p7	6:33415325	GATGCCCGCTGCCTG[C/T]CCAGGTCAGTGCTCC	5252
rs781617995	snp	C/G	4.01171e-05	0.0044785	utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409741	TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTCC	5252
rs781641759	snp	A/C	3.29549e-05	0.00405911	intron-variant, downstream-variant-500B	CUTA, PHF1	GRCh38.p7	6:33416882	AAGTCACACCCACAC[A/C]GTACACACCCTCACC	5252
rs781693450	snp	C/G	1.65201e-05	0.00287398	intron-variant	PHF1	GRCh38.p7	6:33412689	CTGTGACACTGTGTT[C/G]TCTCACAGCTGCCCT	5252
rs781773989	in-del	-/TC			utr-variant-3-prime, upstream-variant-2KB	KIFC1, PHF1	GRCh38.p7	6:33409704	GAAGACGGATCCAGA[-/TC]TGTGTGTGTGTGTGT	5252
rs796783597	in-del	-/A			intron-variant, upstream-variant-2KB	PHF1	GRCh38.p7	6:33412164	AAACTCCATCTCAGG[-/A]AAAAAAAAAAAAAAA	5252