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

PHF21A

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs137936762	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46038730	TGGCTAAGCATGCTA[A/G]CATACTTGCTCAGGT	51317
rs137946119	snp	A/G	0.00953873	0.0683987	intron-variant	PHF21A	GRCh38.p7	11:45943184	CCGGAGTGCAGTGGC[A/G]CAATCATGGCTCACT	51317
rs137963804	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46092803	TACTCTGTTGTCCAG[A/G]CTCAAGTGCAGTGGC	51317
rs138028302	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068358	GGGAATAAATGGGAA[G/T]GGATTTTTTGAAAGC	51317
rs138029116	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46098783	GAGCTTATTTTGGTG[C/T]ACAGGGATTTAAGGA	51317
rs138030745	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035058	AGAGGTTTGCTGCTT[C/T]TTGCATTCCTGAGGG	51317
rs138064031	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084972	GGCGTGAGCCACTGC[A/G]CTGAGCCAAAATCAT	51317
rs138071819	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973525	GCCATTGCCTCCTTA[A/T]ATGTGAAATGAGAGT	51317
rs138078414	snp	C/T	0.0158469	0.0875917	intron-variant	PHF21A	GRCh38.p7	11:45983486	TATACATGTCTGTTG[C/T]TATCTGTGAAAAAAA	51317
rs138087702	snp	A/G	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:46022806	CTTTTTTTTTGAGAC[A/G]GAGTCTCGGTCTATT	51317
rs138098779	snp	A/G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930266	GCGTGCTGCAGACAC[A/G/T]GTCACCCTCACGGAA	51317
rs138105706	in-del	-/C	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46081211	CCAACCATGGGACCT[-/C]CCAAATACACAAGGT	51317
rs138180002	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46003576	TGACATTTTCACGAA[A/G]GGCAGAGTGAGAAAA	51317
rs138232116	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46020384	CCAAGAACCAGGAGC[A/G]CCTGCTCTGACACTG	51317
rs138242314	snp	C/T	0.00350372	0.0417083	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934201	TCTGCCGGGCCAGGA[C/T]GGTGTTCTTCATTTC	51317
rs138297435	snp	A/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46100213	ATGCTAGCCTTTAAG[A/T]CCAAAAATATGTTAT	51317
rs138298718	snp	C/T	0.0252325	0.109451	intron-variant	PHF21A	GRCh38.p7	11:45976632	GGATCACTTGAGCTC[C/T]GGAGTTTGAGACCAG	51317
rs138319583	snp	A/G	0.00943836	0.0680448	intron-variant	PHF21A	GRCh38.p7	11:45953661	AAAAATTCAGAATTC[A/G]TTTTTTATTAAAAGG	51317
rs138320256	snp	C/T	0.00874735	0.0655527	intron-variant	PHF21A	GRCh38.p7	11:46066399	AAAATTAATATGTGT[C/T]CCTTATAAAAAATAA	51317
rs138334566	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968118	AAGTGCCTAGCATAG[C/T]ACCTAGTATGTAGCA	51317
rs138395319	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45955285	TCTTTCTCTCTCCAA[A/C]ACACACACACACACA	51317
rs138405072	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46061231	GTATAGTTTGAAGTC[A/G]GTTAGCATGATGCCT	51317
rs138421329	snp	C/T	0.0236746	0.106192	intron-variant	PHF21A	GRCh38.p7	11:46040253	AACATAATGGTCTCA[C/T]CTCAGTGGAAAAGAG	51317
rs138428861	in-del	-/AAAA			intron-variant	PHF21A	GRCh38.p7	11:45958397	CAAAACCTGGTCTCA[-/AAAA]AAAAAAAAAAAAAAA	51317
rs138433415	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944602	CCCCGCTATCCTGGC[C/T]CTCTTGCTTTTCTTT	51317
rs138448690	snp	A/G	0.0267878	0.112589	intron-variant	PHF21A	GRCh38.p7	11:45998013	AGTTTTGCTCCTATC[A/G]AAACATTTCAGTACC	51317
rs138455095	snp	A/C	0.00953873	0.0683987	intron-variant	PHF21A	GRCh38.p7	11:46046548	TCACTCTGCTTTTTT[A/C]ATGGTTATTAGAAGC	51317
rs138488447	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46052397	ACCAATAAATCTCTT[C/T]TCCTTCAACAACATT	51317
rs138575818	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46001493	AAGCTCCAGTTGGTG[A/T]CTCCGTCACATGCAC	51317
rs138625045	snp	C/T	0.0158469	0.0875917	intron-variant	PHF21A	GRCh38.p7	11:46033980	CAATTTTATATTCCA[C/T]TCAGCAGTGTATAAG	51317
rs138645045	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45977485	AACAGGATGTTTCCA[C/T]GGGTTAAGACAGAAA	51317
rs138646542	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086149	TTTGAGAAAGAGTCT[C/T]GCTCTGTCGCCCAGG	51317
rs138654557	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46015374	GTCAATTTTTGTTTT[C/T]GTTACAATTACTTTT	51317
rs138700816	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46021398	ACCTCACCACATTTT[A/T]AACTATTAACAAGTA	51317
rs138708023	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46117479	TTTGCAGGCTAACTT[A/G]AGTACATCAACCATA	51317
rs138727043	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45985222	TGCATTGATAAGTCA[C/T]ACCAATATTCATCAA	51317
rs138728130	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46072467	AGAGCAACAGAATAG[A/G]AGGAACCTGGGTTCC	51317
rs138744457	in-del	-/AGT	0.0952156	0.196321	intron-variant	PHF21A	GRCh38.p7	11:45991260	GTCTGAATGTATCAC[-/AGT]AGTAGTACCTTGATT	51317
rs138748109	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959862	CAACAGAAAAATAAC[C/T]CAATTTAAAAATTGG	51317
rs138752537	snp	A/C	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46054327	AATCATTAACTCTGA[A/C]AAACTAACAACATAC	51317
rs138766919	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46077910	CCCTAAATCTAATTT[A/G]TTATTTATTTATTTA	51317
rs138821722	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071065	GGTAGATGAATTACT[A/G]TTTTCAATTTCCATA	51317
rs138827729	snp	A/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45973111	TAAAAATAAAAACTA[A/T]ATTAATTAAATGTAA	51317
rs138843746	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953576	GCAGGTGGGGTGATG[C/G]TGCGGCTCTCTGTTT	51317
rs138853591	snp	C/T	0.0146672	0.084371	downstream-variant-500B, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929079	ATCCCTTTTTCATAA[C/T]TAAAGTTTTAAAACA	51317
rs138905214	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045937	AGTTCACAACTGGCT[C/T]TGTTTTCTTGCTTAC	51317
rs138906772	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935842	AGGTATTTTCCCCAG[A/C]GCTCCCATGAGTCCT	51317
rs138917819	in-del	-/GTAT			intron-variant	PHF21A	GRCh38.p7	11:45987274	ATGTATGTATGTATG[-/GTAT]TATGTATGTAACCTG	51317
rs138989186	snp	A/G	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46101777	AATAGCTGGGACTAC[A/G]GGCACATGCCACCAC	51317
rs138997291	snp	A/C	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:45998633	TTCTCCTGCCTCAGC[A/C]TCCCGAGTAGCTGGG	51317
rs139011099	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45957226	TAAGTAATGGATAAA[A/C]CTTGTGCAGAGATTA	51317
rs139020268	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46073032	ATCCTGTTAAATAAA[C/T]TAATAGTTGCTTCCA	51317
rs139023576	snp	C/T	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46110172	GTAATATAAAGTACA[C/T]TCATGAGTATTATCT	51317
rs139060012	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057409	CAGGAGTGTTAATTC[A/G]ATACATATAACAGAT	51317
rs139068892	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123152	GAGCAACAGTGGTGA[A/G]ATGATTTGCCCAAAG	51317
rs139077166	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46011857	TCTCTCTATGCAACA[C/T]AACAAAACAAAAAGA	51317
rs139097770	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067389	AGTGACGTAGTAACA[A/T]TGCAGAAGAGACTTG	51317
rs139102461	in-del	-/AC	0.0314385	0.121371	intron-variant	PHF21A	GRCh38.p7	11:46097826	ATCTCCCTAACTAGA[-/AC]ACACACACACACACA	51317
rs139141045	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016465	TTTGCCTTTGCTTAA[A/G]TTATTCCCTCTCTCA	51317
rs139162091	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46010389	ATCTTGTGAAGATAC[C/T]TTACAGAAGAATAAC	51317
rs139290675	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46096483	CAATGATTTAACAGT[G/T]GTTAAATCCAACAGA	51317
rs139291696	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45993147	ATTTAATTTACATGA[G/T]TAAGAAAAAACAATT	51317
rs139311048	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45940870	GGATAAACGAAGAGG[C/T]GTTCACTTTCCTTTG	51317
rs139376022	snp	A/G	0.0150606	0.0854603	intron-variant	PHF21A	GRCh38.p7	11:45964027	ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA	51317
rs139396631	snp	A/C	0.0111196	0.0737302	intron-variant	PHF21A	GRCh38.p7	11:46088435	CAACAACAACAACAA[A/C]AAAACATAAAAACCA	51317
rs139414158	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932774	TAAAAAAACAGTGCC[C/T]GAACGATGACACAAG	51317
rs139437635	snp	C/T	0.000406532	0.0142513	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965351	GCTAAGCTGTACAGT[C/T]TGAGGTCCAGCGAGT	51317
rs139467692	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113344	GCACACAGTTTCTCT[A/G]GCACATACCGGAAAA	51317
rs139477838	snp	C/G	0.000153988	0.00877328	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933984	TATTTAGTCTCTTCC[C/G]CCTGGTTACAGTTCG	51317
rs139485291	snp	C/T	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46007184	CCATGTGTTCAAAAA[C/T]ATGCAAAGTGATAGT	51317
rs139491575	snp	C/T	9.93526e-05	0.00704744	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965458	CATTGACGACACGGA[C/T]GGGGTGGATGGAATT	51317
rs139496223	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036935	AGGCTAGTCTTGAAC[G/T]CCTGGCCTCAGGCAA	51317
rs139522384	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46023302	GGCTAATTACTGAGG[C/T]CCCTTCTATTTTGAA	51317
rs139545173	snp	A/G	0.00795532	0.062565	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931910	GGAGAGGCCACAACC[A/G]GCCAAGCCGAGGCAA	51317
rs139562439	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042390	ATGTGTGATAGTGCA[A/G]CTCCGGAAAGTTCAT	51317
rs139575416	snp	A/G	0.0130921	0.0798413	intron-variant	PHF21A	GRCh38.p7	11:46104039	CATAGGTAGCTTATG[A/G]CAATTAAATATAGAA	51317
rs139643495	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112737	TCCATCCAACCTTAC[A/G]GAACAACTATCCCCA	51317
rs139691690	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:45955099	CCACTGGTGTTCTCT[C/T]GTATTTCCCCCTTTA	51317
rs139731828	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104817	CAGCACAGTGGTATG[C/T]AGCACGTATGTGATA	51317
rs139741980	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45988014	GACAAGTTGGATATG[A/C]AAATACAATTTAAGT	51317
rs139743387	snp	C/T	0.0310518	0.120672	intron-variant	PHF21A	GRCh38.p7	11:45946469	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	51317
rs139761891	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991598	CACTTTTTCTCCTCC[A/G]CTCTGCTTTTAGAAA	51317
rs139838896	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45970125	CTTCTGTTTCCTCCT[A/G]CACCTAATGGAGAAC	51317
rs139871532	snp	C/T	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:45965217	ACAATGGTGGTGAGA[C/T]GAAGAGCCCTTGAGA	51317
rs139927266	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46055005	TTGCTAATCTTGTAA[C/T]ACAGGACCAGGCTTT	51317
rs139997788	snp	C/T	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:45979449	AAGTGTAAATAAATA[C/T]CTCCAAAAATTCAAA	51317
rs140012226	snp	A/G	0.0248432	0.108648	intron-variant	PHF21A	GRCh38.p7	11:46088924	ACTCGAAGGAAAGCT[A/G]TAACTCCAATTTTAC	51317
rs140019026	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988223	GAAGAGGTAAATATA[A/G]CAGATTATTTAACCA	51317
rs140045105	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46094763	AAATTAGCTGGGTAT[A/G]GTGGTGTGCACCTGT	51317
rs140067410	snp	C/T	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46030457	AATGGGGGCTAATAT[C/T]AGATTTCAATACCAG	51317
rs140133973	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46061706	CAACCTAAACTGGCT[-/G]GTTTTCTAAACCTGT	51317
rs140142221	snp	C/G	3.35864e-05	0.00409781	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45969842	GTTTGGACGTGGAGT[C/G]AGTCTAGGAGGGGGG	51317
rs140147881	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45950852	TGTTTCACTTGTCAC[A/G]ACTAGGTCAGTTTCT	51317
rs140158336	snp	A/G	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:46045487	CACTACTATTACTCC[A/G]GTCTAATTACTTGCT	51317
rs140164173	snp	A/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45940217	TTTTTTTTTTTAGAC[A/G]GAGTCTCTTGCTCTG	51317
rs140182277	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45945314	TTTGTGGGTGAAGGG[C/T]TACTAAGTATTTGAC	51317
rs140229376	snp	C/T	0.0178098	0.0926698	intron-variant	PHF21A	GRCh38.p7	11:45956625	CTAGATTGTTAAAAA[C/T]GTATGAATGTTTACT	51317
rs140269085	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46114531	TCACCATAAAAGTGA[C/T]GGGCTACTATAAAGG	51317
rs140273453	snp	C/G	0.0887219	0.191022	intron-variant	PHF21A	GRCh38.p7	11:46007498	TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCACC	51317
rs140287025	snp	A/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085905	CAGGGCTTATATACT[A/T]GATTATATAACATCA	51317
rs140291263	snp	A/G	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:45983476	CGTGTGTGGTTATAC[A/G]TGTCTGTTGCTATCT	51317
rs140344426	snp	A/T	0.00953873	0.0683987	intron-variant	PHF21A	GRCh38.p7	11:46089765	ATGTCTGAATGTATG[A/T]GAGTATAAAATATCT	51317
rs140345318	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026997	ATGTAGGAAAAGGAA[C/T]CCTTTTCTGAAAAAT	51317
rs140350720	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080254	GCCTTAACCTCCTGG[A/G]CTTAAGTTATCCTTC	51317
rs140358721	snp	A/G	0.00636936	0.0560724	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929617	GGACCCACGGACACC[A/G]GAGAGAGGTGAGGGT	51317
rs140368358	in-del	-/ACAC	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46046746	GCTTTCTACATGTAA[-/ACAC]ACTATAAAACCCAAC	51317
rs140375900	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46000066	TCGATTGACTAGAGA[G/T]CTGAGGACAGTACAT	51317
rs140418275	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46052259	AGCTGCCAGAGGCAA[-/C]CCTCTGCCAGTACAG	51317
rs140442729	snp	A/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:45976338	CAAAATTTCTCTACA[A/T]CTTAAATTTTTTTAA	51317
rs140445879	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46076224	TCTCCTGCCCTATAT[A/G]GAATAAGTCTAATAA	51317
rs140539278	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46069788	CAATGATGCACTTGT[A/G]ATTGAGTTAAATGTT	51317
rs140543084	snp	C/T	0.000153988	0.00877328	missense, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934131	TTGGAGAGGTCGATG[C/T]CGTGGATGAGGCGAA	51317
rs140552281	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062221	GGCACTCAGTGGATT[C/G]TATTAATCTGGAATT	51317
rs140571781	snp	A/C	0.0134861	0.0810011	intron-variant	PHF21A	GRCh38.p7	11:46013044	TGAACCCTATATATA[A/C]TATGTTTTTTCCTAT	51317
rs140584709	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46032052	CAACTCTTAAGTGCT[A/G]CTTTAAAAAGAAAAC	51317
rs140584829	snp	A/G	0.02016	0.0983543	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934744	ATTTAGGAGGATCGA[A/G]GCCCCAAGGACAAAG	51317
rs140660193	snp	A/C	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:46115665	ATTAATATTTCCCAG[A/C]ACAAAATAATATGAA	51317
rs140667299	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46050654	ACAATGTTCAAGAGC[A/G]TAGTCCAAGATCCTG	51317
rs140669905	in-del	-/AAACA			intron-variant	PHF21A	GRCh38.p7	11:45975384	AATAAAATAAAACAA[-/AAACA]AACAAAATAAAATAA	51317
rs140683385	snp	C/T	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:45958226	AAATTCCAGAAAATA[C/T]ACTCTTAAATCATTC	51317
rs140783129	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46004721	GAGGGCTGTATCTGC[C/T]AGGCCTAGAATGCTT	51317
rs140790005	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45957223	CTTTAAGTAATGGAT[A/T]AAACTTGTGCAGAGA	51317
rs140795845	snp	A/C/G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46098834	ATGGGAGTTCTGGGT[A/C/G/T]TAAACCATAAGCACC	51317
rs140807470	in-del	-/TTTTC	0.275464	0.2487	intron-variant	PHF21A	GRCh38.p7	11:46087549	TTCATTTGAAATTCT[-/TTTTC]TTTTCTTCAGAAAGA	51317
rs140815940	snp	A/G	0.119978	0.213528	intron-variant	PHF21A	GRCh38.p7	11:46033408	CAGCTGGGACCACAG[A/G]TGTGCACCACCACAT	51317
rs140867833	snp	C/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:45955971	TAAACTTGTGAAGGA[C/T]TATCAGCCAGAACTA	51317
rs140870481	snp	A/G	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46059189	TTTACGTCCAAGGAT[A/G]TACACTGCAGAGCTA	51317
rs140876547	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45962517	CTGCTGATCGGGCTC[A/G]GTAACCTCTAAGACT	51317
rs140899666	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46081057	TAATTTTAAAAAGAC[A/G]AGTGAATAGGTTGTA	51317
rs140924091	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026113	CTATTCGTACTTAGG[C/T]GAGAGACCTGGGCTA	51317
rs140949919	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46116824	AAAACTTAGCCGGGC[A/G]TAGTGGCGGACACCT	51317
rs140955136	snp	A/G	0.0267878	0.112589	intron-variant	PHF21A	GRCh38.p7	11:45973007	CACTTGAACCCGTGA[A/G]GCAGAGGCTGCAGTG	51317
rs140971307	snp	C/T	3.29506e-05	0.00405884	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979886	TTTGTTTTCAGATTG[C/T]GGCAATGGCTGTATT	51317
rs140988085	in-del	-/TCAAGCAATCTTCTCACT	0.0123036	0.0774623	intron-variant	PHF21A	GRCh38.p7	11:45980610	CTTGAACTCCTGGCA[-/TCAAGCAATCTTCTCACT]TCAGCATCCCAAGTA	51317
rs140989370	snp	C/T	0.00953873	0.0683987	intron-variant	PHF21A	GRCh38.p7	11:46074906	CCTTCAAGTATTAGC[C/T]TACCTAAAAATGATA	51317
rs141013358	snp	A/C	0.00874735	0.0655527	intron-variant	PHF21A	GRCh38.p7	11:46077141	AGTATCCATTGACAG[A/C]AAACCCAAAGCTCCA	51317
rs141044234	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107569	AAGGCTTTAGCACTT[C/T]GTGGATCTAAAGAAG	51317
rs141049547	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46065158	TGTTTAGGTATCTAG[C/T]TTCCAAATGCTCAAG	51317
rs141060827	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45965952	CAATAGCCTTAACTC[A/G]CATTTGAAATTTCTT	51317
rs141117857	snp	A/G	0.0138799	0.0821421	intron-variant	PHF21A	GRCh38.p7	11:46091746	AGAGATGAGGGTCTC[A/G]TTTTGTTGCCAGCTT	51317
rs141129808	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46097511	AATCTACAGCAGTTT[C/G]AGGAGCAAAAGAATA	51317
rs141146711	snp	C/T	0.0119091	0.0762411	intron-variant	PHF21A	GRCh38.p7	11:46028999	TTTCTATTGGATCTA[C/T]AAATTGTACCACAAG	51317
rs141164476	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45995027	GACCTGGGAGAAAGA[C/T]CTAATTGTCAGACTG	51317
rs141244643	snp	C/T	0.00713967	0.05932	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933932	TTCTGTTCTCCTTGC[C/T]GCCGGGATCCCGTGG	51317
rs141266857	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45968496	CACCCTGGAACTACA[C/T]ACATGTTCTGTCCTC	51317
rs141270001	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982693	CAGTCCTCCTCCCCA[A/T]CAGACATCAAACATA	51317
rs141271625	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067414	GACTTGTTTCTAGAT[A/G]TATCAAGTTTTCAAA	51317
rs141280786	snp	A/G	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46083607	GCCTGATGTCCAGCT[A/G]AAGTCTAGAAAGATA	51317
rs141311911	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043781	AGATGAGAGGACCCC[A/G]CTGTCATATACCCAC	51317
rs141357666	snp	C/T	0.0185938	0.0946107	intron-variant	PHF21A	GRCh38.p7	11:46001650	TTTTTAAAATTCCAT[C/T]AGTATCTTGCCAGAT	51317
rs141388105	snp	A/C/G/T	0.000348898	0.0132036	missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934062	GCATTGGCAGGGGGG[A/C/G/T]TGCAGTCCGGGCCAT	51317
rs141411613	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45942142	TTATCTTAAAAATAC[C/T]TTCTGCTGAGTTTAA	51317
rs141416262	snp	A/G	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46060710	TTCCATATAGATGCT[A/G]GATATTAGACCTTTG	51317
rs141426845	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45984457	CTTCAAGTCACAGTT[-/T]CCAAGACAGGTAGTC	51317
rs141450248	snp	C/T	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:45947842	GCCCAGGAATCAATA[C/T]AAAGCCATGACTTAG	51317
rs141500467	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46088156	GGCTACATTTGTAAA[A/G]GATGATTTAACATAT	51317
rs141554262	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46002381	TGCTTCAGAAATAAA[C/T]TAATTTGTAACTTTA	51317
rs141554888	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46072726	TCCTCTGAGGAAGTG[A/T]CATTTAAGCTATGAC	51317
rs141555989	snp	A/C	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46019774	TAAACAGTAGCTCTG[A/C]TCTAAAAATGATAAC	51317
rs141622916	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46079675	GTTCGGTGCAGGGGA[A/G]GATAAGTTCAGTGGG	51317
rs141626720	snp	A/C	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:45944348	GAGAAGCATAGGCAA[A/C]ATGTTAACAACTGAT	51317
rs141651690	snp	A/C/T	0.000202158	0.0100519	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965362	CAGTTTGAGGTCCAG[A/C/T]GAGTCTGGTCCCTGG	51317
rs141686809	in-del	-/AGCCT	0.219648	0.248151	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932148	AGGGCTGATGCAGCC[-/AGCCT]GTACTCCCGCACCCT	51317
rs141736945	snp	A/G	0.0267878	0.112589	intron-variant	PHF21A	GRCh38.p7	11:46014447	TTCCATGTCTTTGCT[A/G]CTGTGAATAGTGTGG	51317
rs141740169	snp	A/G	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:45972343	ATGGCCTAAACATCT[A/G]TCTGGAGATAGATCA	51317
rs141741491	snp	A/G	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46021406	ACATTTTAAACTATT[A/G]ACAAGTATACACCAT	51317
rs141805772	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45966820	GACAGGGTTTCACCA[C/T]GTTGGCCAGGATGGT	51317
rs141843673	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46009570	CTATGTATTACATAA[C/T]TTAATCTTCAAAGCA	51317
rs141886876	snp	C/T	0.0158469	0.0875917	intron-variant	PHF21A	GRCh38.p7	11:46078060	GGCCTTACAAGGCAC[C/T]CATCACCATGCCTGG	51317
rs141917492	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46103163	TGATTTTCAAAATTG[C/T]ATAATTCTTTAACTC	51317
rs141932535	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939345	TAGGGGGAGTTTAGA[A/C]GGACTGGGAAAGAAG	51317
rs141940654	snp	A/C	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46035918	AGCAAAGAGAAGACA[A/C]AGAGAGGTTTTAAGC	51317
rs141957836	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46038906	GATTAAGTTTCCAAC[G/T]CATGAAACTTGGGGG	51317
rs141969672	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043941	TTAAATTATATACTT[A/T]ATGATTTATATCAAG	51317
rs141975302	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958713	TTGAGTCCACGAGTT[C/T]GAGACCAGCCTGGGC	51317
rs141987571	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45999861	TATATAGAAACATCG[-/T]TAACTTTTCTCTTGA	51317
rs142022508	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094226	TTATCTCCAAGGCAT[C/T]TTCTCCAAAAATGAG	51317
rs142085006	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975362	TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT	51317
rs142138238	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46045967	CAGAGATAAAGTACC[A/G]TATTAAAACTCAATA	51317
rs142142808	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037772	TGAGAACTTGAACAA[C/T]ACTTGAAAATTTTAG	51317
rs142161748	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994085	AATGATATACTTCCT[C/T]GTCTACATAGTATGA	51317
rs142204723	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945760	CAAGAAGGTGCAAGT[C/T]GATAAGGAGACAACA	51317
rs142234118	snp	A/G	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:46056518	GCTTTTAAAAAATAG[A/G]TCCTTGTAAACGTCT	51317
rs142241310	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961268	ATGAAGTTAATCAAG[C/T]ATACTTTATATACTT	51317
rs142243135	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097399	ACTGGCCTCTTTTCC[A/G]TACTTCAGACCCTCC	51317
rs142264427	snp	G/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45992942	GCTACCTCAAGTGGT[G/T]GAGAAAGCAGTTGTT	51317
rs142275648	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45976034	CTTAGACTTCCCTAT[A/G]ACTGTTAAAAAACCC	51317
rs142280118	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041030	TGAACATGCCTCTAC[A/C]GTAAATAGGTCGCCC	51317
rs142280119	snp	A/G	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46110426	GTCAAAGGTCTCTAT[A/G]CTGAATCTACATGGC	51317
rs142366586	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048253	ATAAACAGAATCATA[C/G]AGTATAAGGCCTTTT	51317
rs142404612	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45971543	CATACTCCTTACTAC[A/G]GAGAAAGGCAATCTC	51317
rs142411689	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46069257	AAACGAGGAGCTGAT[A/G]TCCTCTGATGTACAC	51317
rs142413568	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932205	CGCACCACAGAGCTC[C/T]GCTGGCCAGTTCCCT	51317
rs142434954	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:46108577	GTGTGTATATATATA[-/AT]TATATATATAAAATA	51317
rs142503675	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46118226	TCTTTTTCATCTATT[A/C]CTACTCCAGTTCCAC	51317
rs142518869	snp	C/T	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46018597	GCCTTTTAAATCCCA[C/T]TAACCTATTTGACTC	51317
rs142519594	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46064386	AGAGCAAAGGAATGT[C/T]TGGTGCTTCACTGAG	51317
rs142562959	snp	C/G	0.0185938	0.0946107	intron-variant	PHF21A	GRCh38.p7	11:45973539	AAATGTGAAATGAGA[C/G]TAAACGCGGAACACT	51317
rs142590467	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46090191	GAGCATAGTGACAAT[A/G]AGGCCAAGGTTTTAG	51317
rs142607836	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46013503	AAGCCACAGAAATGG[A/G]AACTGCAGGTAAGTG	51317
rs142627161	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45969440	CTACTAGTTGGTTTA[A/G]CTGTTGTTTCCTTCC	51317
rs142656020	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45966195	TCTATGTACTGAAGA[C/T]TCACACTTTTACCTC	51317
rs142697763	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45990579	TTCATCTTCTTCCAG[C/T]ATACTCCTAAGTACT	51317
rs142717960	snp	C/G	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:45936153	CATGGTAGTACACAC[C/G]TATAGTCTCAGCTAT	51317
rs142722491	snp	A/G	0.00874735	0.0655527	intron-variant	PHF21A	GRCh38.p7	11:46006046	AAAACAGTCTTTGTA[A/G]ATAAAAAATAATTCA	51317
rs142730304	snp	C/T	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:45986032	GTATTGATTAGACTT[C/T]GGCTTACTTTTTTAA	51317
rs142744198	in-del	-/AGAG			intron-variant	PHF21A	GRCh38.p7	11:45996512	CCCTTTTTGAGAGAC[-/AGAG]AGAGAGAGAGAAACG	51317
rs142747504	snp	C/T	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46083216	ACTTAAAGAAGCCCA[C/T]GTGCATAGGGCCAAC	51317
rs142774916	snp	A/T	0.000543895	0.0164819	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946051	AACGGGGAGGGAAAG[A/T]GAGGGGGAAAATGAT	51317
rs142787547	in-del	-/CT/CTCCCT			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PHF21A	GRCh38.p7	11:46121177	CTCCTCTCTCTCTCA[-/CT/CTCCCT]CTCACTCTCTCTCTC	51317
rs142787919	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46046623	ATATATTTCCCTCAT[A/G]TATCTTCTCTGTCAA	51317
rs142813888	snp	A/G	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46112387	CTGCTAATTCTAAAC[A/G]TTTACTGAGCCCTTA	51317
rs142817626	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46005315	AAATATTGTATAAAA[C/T]TTATACAAATTTATG	51317
rs142948382	snp	C/T	0.000382896	0.0138312	missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934054	AGGTGGCGGCATTGG[C/T]AGGGGGGGTGCAGTC	51317
rs142973301	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959980	AAATGCACATCAACA[C/G]TACTTTGCACCCACT	51317
rs142998426	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014194	TGGAGTCCCTAGTGT[C/T]TACTGTTCCCATCTT	51317
rs143008374	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949559	ATTGTTTTATCTATT[A/G]GTTTTCCCATAAGAA	51317
rs143011014	snp	A/G	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085348	ATATAATGGCATGTG[A/G]AGATAATGTCAAAAG	51317
rs143014906	snp	A/G	0.209997	0.246779	intron-variant	PHF21A	GRCh38.p7	11:45962669	GGCCAAGGCAGGTGG[A/G]TCGCCTGAGGTCAGG	51317
rs143098668	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46052411	TTTCCTTCAACAACA[C/T]TGAATTGAGTTTCTA	51317
rs143099814	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46106581	TTTCAATAATTTGCA[C/T]ATATCCAACTCCATC	51317
rs143124439	snp	C/T	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46007470	AGGTGCCCACGACCA[C/T]GTCCAGCTTATTTTT	51317
rs143124534	snp	A/C	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46068802	CCAGCACCAAAAATA[A/C]GTTATTAGGATAAAC	51317
rs143124954	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941797	TTTGCTAGGCGCTGA[A/G]GACGTATGTTTTTAG	51317
rs143141110	snp	C/T	0.0115144	0.0749975	intron-variant	PHF21A	GRCh38.p7	11:46117839	TTATACTATCCGCAA[C/T]CGCACATCTACTTTG	51317
rs143149900	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46010516	TTTCTTTCTGCTTTA[C/T]GACATTGTTTGGGAA	51317
rs143175909	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028424	CAAACATATTACTTT[A/C]ATAATTAGAATAATA	51317
rs143190838	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011629	TGCTTTTCATTTCTA[A/T]ATTCAAGAAACAGTT	51317
rs143194121	in-del	-/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45995448	CACAGCATGTTTGTG[-/T]TGACAGTTATACTGT	51317
rs143281579	snp	C/T	0.0263992	0.111815	intron-variant	PHF21A	GRCh38.p7	11:46021269	GTCTCACTCTGTTGC[C/T]CAGGCTGGTCTTGAA	51317
rs143304095	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968228	ATTTATTCTCTGCAC[A/C]GAGGCAAGAAGGAAT	51317
rs143319716	snp	A/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:46065070	GAAAGTGTTATAGAG[A/T]CAGACATTGTTAACT	51317
rs143414540	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059764	CAGAGTCTCACTCTG[C/T]TGCCCAGGCTGGAGT	51317
rs143429437	snp	C/G/T	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:45995214	TGGGATACAGTGGAA[C/G/T]GAACCCACTCATCAG	51317
rs143434210	snp	A/G	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:45983622	GCAGAGGTGCTCCTT[A/G]GGTGTGGAGGCCCTG	51317
rs143521159	snp	A/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46050185	TCCTTTTTTCCCCCC[A/T]TAATTTGGCCTAGGC	51317
rs143532389	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45989123	ACTGATTAACTTCAT[A/G]GAATTGGCTCTTCCA	51317
rs143552365	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934874	AAAGAGAGGAAAGAG[A/G]TGTTAAATCTGCATG	51317
rs143561777	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035746	GTGTCTCAGAAGGGA[A/G]ACCAGTAAGTTCAAA	51317
rs143570530	snp	C/T	0.0158469	0.0875917	intron-variant	PHF21A	GRCh38.p7	11:45934300	CCCCTAAGAGCAGAG[C/T]GCCTTCTCTCTGCCC	51317
rs143591811	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078156	GAAGTTTCTCACGGA[A/C]GTAGGATCATTCAAA	51317
rs143613093	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45940489	GTGAGCCACTGCGCC[C/T]GGCAGATTTTAATGT	51317
rs143629966	snp	C/T	0.00128444	0.0253095	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979776	TGTGAAGCAGTCAGG[C/T]TGGGAGAGGCTGCAG	51317
rs143650781	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055217	AGATCTCTTACCCAA[A/G]TATAACAAAGCAGCA	51317
rs143699900	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46071660	CACATCTAGGAATTT[A/C]TCCTAAGACCATCAG	51317
rs143733112	snp	A/T	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:46014250	ACTCCCACTTATAAA[A/T]GAGAACATATAATAT	51317
rs143745708	snp	G/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45958357	AGCTTGAGCTCAGGG[G/T]TTCAAGACCAGCCTG	51317
rs143746782	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46088986	ACAGAAACCTTTTTC[C/T]AATCAAAACTTGACT	51317
rs143843072	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46008883	CACTACTTATTTGAC[C/T]AGTGTTCACCCTCCA	51317
rs143878034	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931043	GCTGGGTTGCATCTC[A/G]TACTCCATACTAGCT	51317
rs143881073	snp	C/G	1.68499e-05	0.00290253	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45969853	GAGTGAGTCTAGGAG[C/G]GGGGATAAACTGTGG	51317
rs143931086	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46061557	GCTTGGTTTTCTATA[G/T]TCCTACAATTAATTC	51317
rs143945395	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937896	ATGAGGCACACTGGA[C/T]TTTAAAGGGTCTTGA	51317
rs143948529	snp	A/G	0.0134861	0.0810011	intron-variant	PHF21A	GRCh38.p7	11:46073699	TGTATACTCTCACTT[A/G]TTATTTCAGAGCACA	51317
rs143956160	snp	A/G	0.030665	0.119967	intron-variant	PHF21A	GRCh38.p7	11:46017066	ACCTCTGCCTCCCAG[A/G]TTCCAGCGATTCTCC	51317
rs143980683	snp	C/T	0.0267878	0.112589	intron-variant	PHF21A	GRCh38.p7	11:45961926	AGAGCCACAGTGTAA[C/T]GTGGTTTCTAATAAG	51317
rs144001145	snp	A/T	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:45964398	TAAGGTCTAGTACCC[A/T]ATGCATAGGTTCCTC	51317
rs144012954	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080597	TTAAAGTTCTTAAAT[C/G]CACATTGTAGTTTTC	51317
rs144058995	snp	C/G	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:46011987	GATGACTATCACCTT[C/G]TTTACTTCCTGTCCA	51317
rs144146541	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119583	TTAGAAATCACTCTC[A/G]GCACATCTGCACCCG	51317
rs144154266	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46011451	GAGCGGAGATGGTGC[C/T]ACTGCACTCCAGCCT	51317
rs144182111	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042662	TAATCCCCAGTGCAA[C/T]TGTATTATGAGGTGA	51317
rs144195995	snp	A/G	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:45982253	TAAGCCACCACGCCC[A/G]GCTGAGAGGTTTTTA	51317
rs144203123	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:45988047	AGTGATGATGCTAAA[C/T]TGGAGGAGGGGAAAG	51317
rs144216894	snp	A/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46047401	TAAGGTATTTTATAA[A/T]TTTTTTTTATTAGTT	51317
rs144251438	snp	A/G	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46088906	TTCATTACGATTCTA[A/G]TAACTCGAAGGAAAG	51317
rs144262108	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975357	TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT	51317
rs144289321	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111530	GTTTTCTTAAATAAA[C/T]ATGGTAGCCCTCAGC	51317
rs144297315	in-del	-/A	0.0260105	0.111035	intron-variant	PHF21A	GRCh38.p7	11:46081391	CCACAGTCTTCAATG[-/A]AAAAAGCTCTTGATT	51317
rs144307982	in-del	-/AG			intron-variant	PHF21A	GRCh38.p7	11:45996512	CCCTTTTTGAGAGAC[-/AG]AGAGAGAGAGAGAAA	51317
rs144322527	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46040386	AGACAATAAAAGTTT[C/T]TTTTAGCATTCTTTA	51317
rs144322699	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037173	TAATTCTGACTAATT[C/T]GGTGCACATCCCTAC	51317
rs144363809	snp	A/G	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46104206	CTCTGGGGTTCTACA[A/G]TTGTTTCCACTAGTT	51317
rs144437609	snp	A/T	0.0248432	0.108648	intron-variant	PHF21A	GRCh38.p7	11:45947043	TGACAAACATCCTGA[A/T]AAACTACATCTCTAA	51317
rs144495709	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023993	TCACTGAATGGCATA[C/G]AGCATGTAGCAACCT	51317
rs144558820	in-del	-/TTCT			intron-variant	PHF21A	GRCh38.p7	11:45969502	GAAGTGTTAATTGCA[-/TTCT]TTCCCCACTGCCAGG	51317
rs144566788	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45994642	AGAGTGGTTATGTTT[C/T]AGGCTTTGTAAGAAC	51317
rs144597372	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45978003	TTAGTTTTCTCTTCT[-/A]AAAAACAGAGATGGT	51317
rs144598265	snp	A/C	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:45977595	AGAGAACAACCTAAC[A/C]CAATTCTGTTTAAAA	51317
rs144616740	snp	C/T	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46062376	TCTTAAAATTTTTCT[C/T]TATTCTACTGTCTAT	51317
rs144643799	snp	C/T	0.0267878	0.112589	intron-variant	PHF21A	GRCh38.p7	11:45963561	AAGCACCTTCTACAA[C/T]TTATATTTTTGTAAT	51317
rs144659872	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46059221	GCATACAACAGTAAA[A/C]AACTGGGAATAATTT	51317
rs144681640	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45954470	CTGTCTATATAATCC[A/G]TCAGAGGAGAGATGC	51317
rs144727394	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45971959	AAGGATTAGCATGTC[C/G]CCTCTGAGGTAGTTA	51317
rs144737441	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46054661	CTGTTGAGAAAAATC[A/G]TTACTATTCAAATCA	51317
rs144748969	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46077411	TCAAAAAAAGAATAC[G/T]ATTTTAGATGAGATA	51317
rs144759713	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991554	ACAGCTGCAGTAAGC[G/T]TATACACACACACAC	51317
rs144768762	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46093245	CTCCACTATATGCTA[C/T]GCTCTAAAACTACAT	51317
rs144784051	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45982859	AACATAAACATGACA[C/T]CTGCCAAAAAATAAA	51317
rs144784888	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024145	GATTTTATATGTTGG[A/G]CTAACTGAGTTGCTG	51317
rs144925907	snp	C/G	0.0107246	0.0724382	intron-variant	PHF21A	GRCh38.p7	11:46036232	ATTGTGGTAGACTGT[C/G]GTAAAATTTACAGTC	51317
rs144966202	in-del	-/T	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:46068013	AATCAGGTAAAAAGG[-/T]TAAGAAAATTCCAGG	51317
rs144966693	snp	C/T	0.000924455	0.0214796	synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934034	GGGGGAAGGGGCCGG[C/T]GTGGAGGTGGCGGCA	51317
rs144974596	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018928	GCAAGACTTTTTATG[A/G]CAAAATCAATGTATC	51317
rs144976266	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46081105	CCTTTAGTAAAATGT[A/C]TAATCTTTGGTGTAT	51317
rs145019364	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46097019	ACTCCACATCTACTC[C/T]GACAGCCAACCATGT	51317
rs145068383	snp	C/T	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:45949292	CTTCACAGAACTGGC[C/T]AAGTACAATCAGGGT	51317
rs145092584	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46109153	TTTGGACATTTAAGA[C/G]CAAGGGCTCAGGAAT	51317
rs145093641	snp	A/G	0.0228947	0.104514	intron-variant	PHF21A	GRCh38.p7	11:46001731	GGGAGAATAAAACCA[A/G]TAAGAAACCTTTCTG	51317
rs145113140	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45951559	TTGAAATGACATACA[C/T]TTTGTGGTTGCCAAC	51317
rs145167196	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100866	GGGAGCACATAGCAA[C/G]TTTCTAACCACTGTT	51317
rs145172014	snp	A/C	0.000153988	0.00877328	missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934093	TGGAGATGGCCCCCA[A/C]AGTGGCCTCAGAGTC	51317
rs145192247	snp	C/G	0.00874735	0.0655527	intron-variant	PHF21A	GRCh38.p7	11:46049020	TGTCTGTTAGGGAAT[C/G]GCTAAACTAGCTCTG	51317
rs145217025	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45955123	CCCTTTATACTAAAC[A/G]CTATGTAAGAGTGGG	51317
rs145226218	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076405	GGCTTTAAGACAGGT[A/G]ACAAGGTACACGCAG	51317
rs145246824	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941447	CATCACACATCATGC[A/G]ATATCTGGTAAACCC	51317
rs145255856	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961017	CATTTTCTATTGTCA[A/G]TTATTATCATGCTTG	51317
rs145288953	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105136	AGGCAGAGCAGGAAG[A/T]CATTTGGCCACAGTC	51317
rs145306787	snp	C/G	0.0185938	0.0946107	intron-variant	PHF21A	GRCh38.p7	11:45962599	TTAGACCAAAAAGAA[C/G]AGAGAACATTGGCCA	51317
rs145321178	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113077	TTAGAGGGCTGGGAA[C/G]CTGTGTATAATAAAA	51317
rs145322248	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46043906	CAGAAAACAGTAAAA[G/T]ATGGATCGCAGCAAC	51317
rs145328083	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46115470	GAAAACATAAGCTAT[C/T]TAAGAAATAATTATC	51317
rs145351106	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085904	TCAGGGCTTATATAC[C/T]AGATTATATAACATC	51317
rs145396887	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45956743	CAAACAAAAAAGGCA[A/G]TATTACAGGAAATGA	51317
rs145400983	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46027252	GCTAACAGGTACAAC[A/G]TGAACAGGCCAAGGA	51317
rs145405707	snp	C/T	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:46030933	AGAGAAATTGCTGAT[C/T]TTAAAACAGTAGCAT	51317
rs145407885	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013479	GCCTCAGCTGACCGT[A/G]AGTAACTAAAGCCAC	51317
rs145439289	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45956598	AAAAATCTAAGCTGG[A/G]GTTAATTCAAACTAG	51317
rs145465811	snp	C/T	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:45973514	TTATTCTCTTTGCCA[C/T]TGCCTCCTTAAATGT	51317
rs145467937	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46032665	TGAAAAGGCTATATA[A/T]ACTTTCATCAATAGA	51317
rs145477372	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049989	ACCATATTCTATCAT[A/G]TATTTCATGTAGTCA	51317
rs145509780	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46074393	GATAAGGTAATTCAG[A/C]TTTTAGTTATTAAAG	51317
rs145519514	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45970491	AATTTAGATATATTT[A/C]TCCCAAGCTTCTGAG	51317
rs145522756	snp	A/G	0.00953873	0.0683987	intron-variant	PHF21A	GRCh38.p7	11:46114125	CATCCCCACACACAC[A/G]CGCTTCTACAAAGAA	51317
rs145583555	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043761	TGTCTGCATCTCCCA[C/T]TCAGAGATGAGAGGA	51317
rs145616055	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46067590	AATAAGAATATTCCA[-/C]CCCCCCACAAAAAAA	51317
rs145691748	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46015592	CAGCTTAAAACACAT[C/T]GTACAGTTGTATAAA	51317
rs145708413	snp	C/G	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46070372	GTCTCACTGTGTTGC[C/G]CAGGCTGGAGTGCAG	51317
rs145712083	snp	C/T	0.0221141	0.102801	intron-variant	PHF21A	GRCh38.p7	11:45972503	AATTAATTGGCCAGG[C/T]GCAGTGGCTCACACA	51317
rs145738714	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45984512	AGCGATACTATCAAC[A/G]TGTTCACACGACAGC	51317
rs145743770	snp	C/G	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:45976499	TTTTGGCAGGGACCA[C/G]TGCTCTTTGTATACC	51317
rs145749596	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45988440	GCCTTACATTTAAAC[A/G]AAAGTAACACTTGTA	51317
rs145770442	snp	C/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46051504	TCCTTCTGGGGCCTC[C/G]AGAGATAAATGGGTT	51317
rs145831781	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008073	GGTGAAAATTAACAC[A/G]AAGTGAAGTTCAGAA	51317
rs145865564	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45980533	GATAGTGTCTCTCTA[A/T]ACTGCCCAGGTTGGA	51317
rs145901883	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116686	ACAAAAATTTAGGCC[A/G]GGCGTGGTGGCTCAC	51317
rs145903197	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46039392	TAAATCAATATATGC[A/G]TGGCTGTAAAAAGTC	51317
rs145926527	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46099209	CACAGTAAACCCAAC[-/T]ATAGCCAGAAGCTTA	51317
rs145950672	snp	C/G/T	0.0150874	0.0857668	intron-variant	PHF21A	GRCh38.p7	11:46064776	ACAATTTTTAAATAC[C/G/T]AAAAAATTAAAAAAT	51317
rs145992986	in-del	-/ATTTTATG			intron-variant	PHF21A	GRCh38.p7	11:45940655	TTTTCTTCCTTCATT[-/ATTTTATG]ATTAAAATCAGGCTG	51317
rs146028864	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45969707	AATGTTTAGCTAAGC[A/G]GGATAGACAGCTGGG	51317
rs146029891	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46068787	AAGTCATTCCATTTG[C/G]CAGCACCAAAAATAC	51317
rs146033545	snp	A/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46072184	TTCCCAGTATTTATT[A/T]CCCAATTCTTACTCA	51317
rs146039628	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974578	CCCATCTCATTCTCC[C/T]GAGTACCTTGGACTA	51317
rs146048858	in-del	-/A	0.0267878	0.112589	intron-variant	PHF21A	GRCh38.p7	11:46012775	GGCCTGCTTAAGGCC[-/A]AACTCATTGTCTTCC	51317
rs146113428	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945264	TTTGTTGAGGTTCAT[C/T]TAAACATTTAGAGCA	51317
rs146151805	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45991826	ATATCTTTACCTCTA[C/T]AGCACTGCACAGAGA	51317
rs146162606	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45940056	CCTCCACCACCACTA[A/G]TGAAGGAACACATCG	51317
rs146172290	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46072862	ACAGTAACAAGCAAC[A/T]AACTTCGGAATGTTA	51317
rs146214688	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46068803	CAGCACCAAAAATAC[A/G]TTATTAGGATAAACT	51317
rs146235374	snp	A/C	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45968775	TCTCTACTAAAAATA[A/C]AAAAATTAGCCGGGC	51317
rs146265929	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016119	TAATGTATTACGCTA[C/T]CAAGTAGTTATGATG	51317
rs146271727	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46010375	TATACCTCGCAACAA[C/T]CTTGTGAAGATACTT	51317
rs146271761	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46070943	CACTTATTATCAATA[C/T]ATGCTATTAATGTGA	51317
rs146290538	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45974424	CAAACGACAAATTAT[A/T]ATTATTATTATTATT	51317
rs146291627	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102848	AAGGTTTTGATAATA[C/G]CTCAGTATCTCCCTG	51317
rs146306676	in-del	-/T	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46118377	CAATGTCAGTCAAAC[-/T]GTAAATACTATTATG	51317
rs146332874	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46095108	TTTAGACTAATGATT[C/G]TTAAACACTGTGCAC	51317
rs146386346	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46041482	GGGAAACTAAGGGGT[A/G]ATCTGAAAGTCAGAA	51317
rs146387328	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46013731	CTATTGCTTATGGGC[G/T]AAACCTAGGAGCAGG	51317
rs146391141	snp	A/G	3.29511e-05	0.00405887	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946015	CGACCTATATACCAA[A/G]AGAAGGGAACAAAAG	51317
rs146396740	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46046093	GATTACCAAACTTAT[C/T]TGAAAGCTGAAGGCT	51317
rs146409559	snp	C/T	0.02016	0.0983543	intron-variant	PHF21A	GRCh38.p7	11:45964626	TTTCTCATCACTAGT[C/T]GTTTTTCAAATAGGA	51317
rs146461356	snp	A/C	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:46057926	TAACTACCAACCTGA[A/C]AGGCACAAATCAAGA	51317
rs146495233	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46033363	TCTGCCTCCTAGGCT[C/T]GAGGGATCCTTCCAC	51317
rs146534502	snp	A/G	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:45988167	TGAGATAATGTAGGA[A/G]GTCACATTTTCACAG	51317
rs146575008	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037596	TGCGGTGAGCCGAGA[C/T]CGTGCCAGCGCACTC	51317
rs146583163	snp	A/G	0.0263992	0.111815	intron-variant	PHF21A	GRCh38.p7	11:45982372	TATTCTGCTAGCACT[A/G]CCTCTCTGAGTAAAT	51317
rs146597431	snp	A/G	0.000397442	0.0140912	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965546	AAGCTGAGGAGCTGC[A/G]AGCATGGGAGGTGGT	51317
rs146615242	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46059426	ACCAATCTCAATTTT[A/T]TTTATTTATTTATTT	51317
rs146634008	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933603	TCTCCTCCCTCCGCC[C/T]GTCCCTGCTCCCCAC	51317
rs146654582	snp	A/G	0.00874735	0.0655527	intron-variant	PHF21A	GRCh38.p7	11:46011637	ATTTCTAAATTCAAG[A/G]AACAGTTTTGGTTTA	51317
rs146692322	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46065077	TTATAGAGACAGACA[C/T]TGTTAACTTTCTTGA	51317
rs146696376	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46007496	TTTTTGTATTTTTAG[C/T]AGAGATGGGGTTTCA	51317
rs146734668	snp	C/T	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084501	TAAGAAATGAAAAAC[C/T]AAAAAAAGGGTTTAA	51317
rs146775738	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036831	AGGTCATCTGCAAAT[A/G]ATGATGATATACATC	51317
rs146779650	snp	C/T	4.94752e-05	0.00497344	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934129	GTTTGGAGAGGTCGA[C/T]GCCGTGGATGAGGCG	51317
rs146812621	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026827	CACTCAGCAGAGCCA[A/G]CATCACGAAGAATGC	51317
rs146816431	snp	C/T	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:46031989	TCTTCCACACTAACA[C/T]GAAAACCACAGCTTT	51317
rs146821133	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45934336	GAAGAAGCTCTGCTG[A/G]CTGCTGTGCAGCCCC	51317
rs146855468	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46115506	TAAATTCAATGCAAT[A/G]TTAACATATTATCTC	51317
rs146889561	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971197	CGTCTGGAGGTTGAC[C/T]GGTGTGTTCTGCACA	51317
rs146891624	in-del	-/TA/TATATATA			intron-variant	PHF21A	GRCh38.p7	11:46108567	AAATGTGTGTGTGTG[-/TA/TATATATA]TATATATATATATAT	51317
rs146922729	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45937126	CCGCTGCACCACAGG[C/T]TGCAGGATGAGGACA	51317
rs146923855	snp	A/G	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:46098580	TTCCATAGCTCTCAC[A/G]AAGCTGTTTTCTGAG	51317
rs146924202	snp	A/C	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46034858	ATGTGACCCTGGCCA[A/C]ACAAATCAAAGTACT	51317
rs146932386	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45942779	TATTCTGCTGCTCCT[C/T]GGAGAGGGGTGTGCC	51317
rs146960517	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46092016	AATGCGTTTGAAGTA[C/T]AGCTACGTGAAATTA	51317
rs146968192	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46101859	CGTGCTGGTCTCCCT[-/C]TTTTTTTTTTTTTTT	51317
rs147006277	snp	C/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46038525	CAGTTGTGTGATTAT[C/G]TTTATTAGTTTACTG	51317
rs147021868	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45949000	TGTGGTTATTACTAA[C/T]ACTGGCACAAGCTAA	51317
rs147038491	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967216	CTACTAAAAATACGA[A/G]CATTAGCCAGGCATG	51317
rs147110091	snp	C/T	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46065540	CCTTATTTGAATCAA[C/T]AAATTCACTTACTAT	51317
rs147160942	snp	A/G	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46035827	AGAAAGAGAGAGAGA[A/G]AAGAGAGGTTGGAGA	51317
rs147175458	snp	A/G	0.0185938	0.0946107	intron-variant	PHF21A	GRCh38.p7	11:45978068	GCACTTTGGGAGGCC[A/G]AGGCGGGCAGACCAC	51317
rs147266210	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46061669	CTTAGCTTTGTTTCT[C/G]CTAAGTCCTCCATCC	51317
rs147270171	in-del	-/AAAAAAAAAAAAAAAAA			intron-variant	PHF21A	GRCh38.p7	11:46088417	TCCAATAACAACAAC[-/AAAAAAAAAAAAAAAAA]AACAACAACAACAAC	51317
rs147282132	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46004213	TGAATTATGCATACT[A/G]GTAAGAAATTTCATC	51317
rs147308885	snp	C/G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46081030	ACCTGCTGTGTGGTA[C/G/T]GCTCACTGGACTAAT	51317
rs147378528	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087024	TCAAACTGAAGACCT[A/G]TAAGATAATAATACT	51317
rs147393274	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005847	AAAAAGAAACACTTC[C/T]AATGAAATGTGGAAA	51317
rs147406056	in-del	-/TGTG			intron-variant	PHF21A	GRCh38.p7	11:46030850	TGTGTGTGTGTGTGT[-/TGTG]GTGTGTGTGTGTGTG	51317
rs147414161	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46112397	TAAACGTTTACTGAG[C/T]CCTTATTATGTGCCA	51317
rs147424018	snp	A/G/T	1.65452e-05	0.00287616	PHF21A	11	allele_origin=G(germline)/A(somatic)	11:45934199	CTTCTGCCGGGCCAG[A/G/T]ATGGTGTTCTTCATT	51317
rs147438481	snp	A/G	6.61551e-05	0.00575093	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953580	GTGGGGTGATGGTGC[A/G]GCTCTCTGTTTGTTT	51317
rs147478433	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46010902	GTGAACAGCATCATA[C/T]CAGCTCCTTTCTCTC	51317
rs147482023	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45954859	GGCTACATGAGACTT[C/T]GGTCCTACAAACAAG	51317
rs147483002	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118886	GCTGACCTATTTATT[C/T]CTATTGCTTAGAGTG	51317
rs147500718	snp	A/G	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:46029857	TATACAGTAAAAATA[A/G]TAACAAAGGCATAGA	51317
rs147570145	snp	C/G	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:46105841	AGAATTTTTGCTTCA[C/G]ATTCTGAATATCTTG	51317
rs147604350	snp	A/G	0.0150606	0.0854603	intron-variant	PHF21A	GRCh38.p7	11:45993886	ACACCGACAGTGCCT[A/G]TCTGAGATGAATTTC	51317
rs147638720	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46043909	AAAACAGTAAAAGAT[A/G]GATCGCAGCAACTGC	51317
rs147642157	snp	A/G	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46049219	GTTCCCATCTCTAAG[A/G]GAAAGTAATACAGAA	51317
rs147653802	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45939740	CAGAATAAAGCAGAT[C/T]TACTTAAAATTGGAA	51317
rs147745613	snp	C/T	0.0298908	0.118541	intron-variant	PHF21A	GRCh38.p7	11:46074753	GGTGATCCACCCACC[C/T]TGGCCTCCCAAAGTG	51317
rs147840395	snp	C/T	0.0678174	0.1712	intron-variant	PHF21A	GRCh38.p7	11:46097469	CTCCAAATATCTTCA[C/T]GGCTCACTCCCTCAA	51317
rs147844953	snp	A/C	0.0221141	0.102801	intron-variant	PHF21A	GRCh38.p7	11:45994993	CACAGAAATGTGTAT[A/C]ATCTCTGTGCTATAT	51317
rs147855084	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45999923	TTGTCTTATCCTCTG[C/T]GCTAAGAGAAAGTCG	51317
rs147855198	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45942016	GCCTCTCAAGTGTTA[C/T]TGTTTAATTAATGTT	51317
rs147856081	snp	C/G	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46104519	TTTCTATTTTTCCCA[C/G]AGGTATTCACAAATA	51317
rs147879950	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45958394	ATGACAAAACCTGGT[C/T]TCAAAAAAAAAAAAA	51317
rs147918963	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45972194	GATCAGAAGATGAAC[C/T]GAGGTGAGAGGACTT	51317
rs147954904	snp	C/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46019361	CACTTGAGAACTAAT[C/G]CAGAAGCTAACTTTC	51317
rs147958121	snp	A/G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46024706	TCAGGAGGCTGAGGC[A/G/T]GGAGAATAGCTAGAA	51317
rs147993479	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46079319	CTTCTGTGATCCATG[C/T]AATAGGCTCAGGAGA	51317
rs148023680	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934901	CATGCCATGGGTAGG[C/T]ATGGTGAGGAGGAGA	51317
rs148103160	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014422	CACTGTTGATGGACA[C/G]CTAGGTTGATTCCAT	51317
rs148136397	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46093639	TTCTTAACACTACTG[A/G]TATCTACAGGACTCT	51317
rs148137663	in-del	-/TC			intron-variant	PHF21A	GRCh38.p7	11:46010972	AAAAAACTTTCTCTT[-/TC]TCTCTCTCTCTCACA	51317
rs148155056	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46116823	CAAAACTTAGCCGGG[C/T]GTAGTGGCGGACACC	51317
rs148163974	snp	C/G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008999	TTTTTTTTTTGGAGA[C/G/T]GGAGTCTCACTGTCG	51317
rs148206958	snp	C/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:46028786	ACCATGTTGGTCAGG[C/T]TAGTTTCGAACTCCT	51317
rs148225794	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46044461	CTCCCCTTTCCACCC[C/T]CATTTGGATTTCATA	51317
rs148263326	snp	A/G	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:45975038	ATGGACTCAGGCTGG[A/G]CACAGTGGGTCATGC	51317
rs148321076	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968489	ATTTCTCCACCCTGG[A/C]ACTACATACATGTTC	51317
rs148380174	snp	C/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:46040592	GTTTAGCAACTAATA[C/T]AATCTAGTGCACCAA	51317
rs148421329	snp	C/T	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:45970927	TCCTTGGTGTCAGGA[C/T]GCTTCTGTAGTGATT	51317
rs148421528	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46068942	TGGCACGTTATTAAA[G/T]TATAAGTTACTCAAT	51317
rs148431981	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45973741	CCTTGTTTTCCATTT[-/A]AAACATGTCGATTTA	51317
rs148452083	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46005928	CAGAACTCTCAAGAA[C/G]AGTAAGAAAAATAAA	51317
rs148474957	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46063566	CAAGCCATAGTTTTA[C/T]CAATCCCTGCCCTAC	51317
rs148510705	snp	C/T	0.0119091	0.0762411	intron-variant	PHF21A	GRCh38.p7	11:46083112	TCACTCAGAAAAAGA[C/T]GAGCTTGTTTTTGTA	51317
rs148516001	snp	C/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:45980712	TAACACAGATACTAG[C/T]CATAGTAATTTTTAT	51317
rs148520597	snp	A/G	0.00130106	0.0254723	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946039	ACAAAAGGGAAAAAC[A/G]GGGAGGGAAAGAGAG	51317
rs148536705	snp	C/T	0.0244538	0.107838	intron-variant	PHF21A	GRCh38.p7	11:45999099	CCCAAAGTGCTGGGA[C/T]TACAGGCGTGAGCCA	51317
rs148557580	snp	A/G	8.37402e-05	0.00647017	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934035	GGGGAAGGGGCCGGC[A/G]TGGAGGTGGCGGCAT	51317
rs148569754	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073900	ATCTCAAGTTACACT[A/T]TAAAAGCACTAGACC	51317
rs148572056	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46035835	AGAGAGAAAAGAGAG[C/G]TTGGAGAAAGTAGGT	51317
rs148625216	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017342	GAAAAAATCAGATTT[C/G]TTTTTTTAGCACTCA	51317
rs148678539	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46011561	TCTAAGATACTTTCT[C/T]GCTCTGGAAATCTAG	51317
rs148683230	snp	A/G	0.108755	0.206276	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119871	AAAGAGTCCCACTCC[A/G]CGCGCCCCTCCCCCC	51317
rs148692721	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45961093	TCTGTTATACTCATG[A/T]TCCCACTGAAAGTGG	51317
rs148713359	snp	G/T	0.00874735	0.0655527	intron-variant	PHF21A	GRCh38.p7	11:46047617	AAGCATAATTAAGAG[G/T]CTGAAAGATATTATT	51317
rs148727925	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46031754	AATAGTGTCTGGAAA[A/C]GAATGCAATAATTTT	51317
rs148736290	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111596	CTGGAATAAGATACT[C/G]GCTAAGCAAGTAAGA	51317
rs148783451	snp	C/G	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:45987446	GTGGGCGAATCACAA[C/G]GTCAGGAGTTCGAGA	51317
rs148787024	in-del	-/ACAC			intron-variant	PHF21A	GRCh38.p7	11:46099523	CTATAGAAAAATTAG[-/ACAC]ACACACACACACACA	51317
rs148817669	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46050085	CCCAGCAGAGTTAGC[A/G]ATTGCCACTAGGGAT	51317
rs148927461	snp	A/G	8.23662e-05	0.00641688	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971248	CTGACTGTTGATGGC[A/G]GTCACCATAGCAATG	51317
rs148943112	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973408	CTAGGGAGTTACTTA[A/T]CTCTATTTTTCTGCC	51317
rs148964526	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46071314	TAAACACATTTAGAG[C/T]AGACCTAACCAAACC	51317
rs148975167	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008714	AGGAAAATAATAATA[A/T]ATGTTTTACATATCT	51317
rs148998189	snp	C/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:46065427	AACAGCAGTGGTTGC[C/T]GACATGCTGAGCATG	51317
rs149006078	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46096289	AATTAAAAAAAAAAA[-/A]CCCTCTTGACTCCAT	51317
rs149008108	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45957752	AACTAAATTCAAAGC[-/A]AAAAAAAAAAAAAAA	51317
rs149031822	snp	A/G	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46001186	ATCACAGAAGTCTAA[A/G]AAGAAAAACTTAAAG	51317
rs149031990	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46106433	GCTTTTTAGTATCAA[A/G]TCCTGATAAGTTAAC	51317
rs149041324	snp	A/C	1.64735e-05	0.00286993	intron-variant	PHF21A	GRCh38.p7	11:45949376	ACTGGAACATGAGGG[A/C]AGGGCCAGATGCTGG	51317
rs149085544	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46097255	CTCTGCTCAAAACCC[A/T]CCAGTGGCTTCCCAT	51317
rs149089014	snp	A/G	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46037598	CGGTGAGCCGAGATC[A/G]TGCCAGCGCACTCCA	51317
rs149191110	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059492	GTGCAGTGGTATGAT[A/C]ATAGCTCACTGTAAC	51317
rs149246288	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46034761	CTGCAGAAACCAACA[C/T]GTCATATGTGTAAGA	51317
rs149291896	snp	A/C			downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929229	ACCCCCCCGCCCCCC[A/C]CCCCCAGACAGCCAG	51317
rs149312875	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45977522	ATGTAACAGGAAACA[A/G]TGAATTCTACCACAC	51317
rs149348170	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054509	TGATTCAACTGGTCT[A/G]AGGTGCAGCCCTGTA	51317
rs149410030	snp	A/C	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46093085	TAGATTGTAAACCAC[A/C]TACACAAAAGCTATT	51317
rs149457924	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085117	ACTCAAAATGGGGAA[A/G]TTCTGGTATAACTTA	51317
rs149472218	snp	C/T	0.0134861	0.0810011	intron-variant	PHF21A	GRCh38.p7	11:45937766	GATTACAGGCCTGAG[C/T]CACCACGCCTGGCCC	51317
rs149491141	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46073612	GACACTGTTTTTGCA[C/T]ACGTTTACACGCCCA	51317
rs149508155	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46011416	ATCGCCTGAGCCCAG[C/T]AGGTGGAGGTTGCAG	51317
rs149526820	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46028369	GTGTTAAGCTTACAG[A/G]CAATTCTCACTTTGC	51317
rs149544562	snp	C/T	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46068443	GTGGTGTCAGTTATA[C/T]TGGCTCCTAAAAAGC	51317
rs149552621	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46111117	ATCACAACTATGTGG[C/G]GGGGGAGGCTAGTAT	51317
rs149561785	snp	A/G	0.0126979	0.078662	intron-variant	PHF21A	GRCh38.p7	11:45968167	TTATTACCATTATTG[A/G]CAATGTCTTAACTGT	51317
rs149567292	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45954006	TTTTTTGTTGTTGTT[G/T]TTGTTTTGAGATGGA	51317
rs149588947	snp	C/T	3.34829e-05	0.00409149	synonymous-codon, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934223	CTTCATTTCCATGCA[C/T]TTCTGCAGCAAATGA	51317
rs149612103	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100777	GTCTACCATTACCTT[A/G]TAGTGACTCCTAATG	51317
rs149615090	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46040277	AAAAGAGAGGAAGGA[C/T]GGAGGCAGGGTGGGG	51317
rs149618563	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45945215	TGCTCAGCAGAGTAG[C/T]GCTCAGTGAGTATCT	51317
rs149654239	snp	C/T	0.0372196	0.131242	intron-variant	PHF21A	GRCh38.p7	11:46113694	AGTTGGGCGTGGTGG[C/T]GCACGCCTGTAGTCC	51317
rs149661811	snp	G/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:45970260	CTGCTTAGCCAAATA[G/T]GCTTTTTCCTGATAT	51317
rs149670458	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46049488	ACTGGTAGAGGGAAA[C/T]AGATGGCTTCTAAAA	51317
rs149701129	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023303	GCTAATTACTGAGGC[C/T]CCTTCTATTTTGAAC	51317
rs149723916	snp	C/T	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46043584	CTGCCAAACTGTTCT[C/T]CATCTCTAAGGCAGT	51317
rs149810589	snp	A/G	0.0279526	0.114869	intron-variant	PHF21A	GRCh38.p7	11:45988387	TAGCAGGCAGTATAT[A/G]TCATGTAGAAAATAT	51317
rs149812378	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46065376	TGTTGATGTGTGAAG[A/G]TGTAAAGCCTGGCAC	51317
rs149863118	snp	C/T	0.00111971	0.0236347	intron-variant	PHF21A	GRCh38.p7	11:45979757	TTCCATCCACACATT[C/T]ACCTGTGAAGCAGTC	51317
rs149866605	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057430	TATAACAGATGCCCA[C/G]AGCATTAGGGCTTAA	51317
rs149880029	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46000429	ATGACCATTAGCTGC[A/G]ATATGGGACTAAAGA	51317
rs149898933	snp	A/G/T	0.000386905	0.0139035	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933999	CCCTGGTTACAGTTC[A/G/T]CTGTGCAGCTCTGGG	51317
rs149901976	in-del	-/AGCTTTA	0.206336	0.246157	intron-variant	PHF21A	GRCh38.p7	11:46000499	TGAATAATTTTAAAC[-/AGCTTTA]AGCTTTAAAGACTCT	51317
rs149931947	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45993601	TCACAGGAGGTTGGG[C/T]GGCATCCAAGCAGAC	51317
rs149934794	snp	A/C	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46096952	AAATGGTAACTCCAC[A/C]CCCTCAGAAGAAAAA	51317
rs149963060	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45987658	AGAGCAAGACCCCGT[C/T]TCAAAAAAAAAAAAA	51317
rs149987752	snp	C/T	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46088815	TAGGCTTTTCTGTTC[C/T]CAAATTCTCTAAGGA	51317
rs150020599	snp	C/T	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:45941444	CATCATCACACATCA[C/T]GCAATATCTGGTAAA	51317
rs150029824	in-del	-/AT	0.20511	0.245937	intron-variant	PHF21A	GRCh38.p7	11:46024014	GTAGCAACCTGTAAC[-/AT]GTGGGAACACTGATG	51317
rs150071758	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933366	CTTGCACGAGGCCCC[C/T]GCCAGAGGTGATTAA	51317
rs150108211	snp	C/G/T	0.00557861	0.0525638	intron-variant	PHF21A	GRCh38.p7	11:46100120	AACATGCCTCAATCA[C/G/T]GCTGATAAGTAAGTA	51317
rs150111211	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45997114	TCTGAAAGTGTTTGG[C/T]GGAGAAATGTTTGTT	51317
rs150120810	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45944535	GCCCTGCGCAACTGG[C/T]CCAGCCACTTCTGAG	51317
rs150131940	in-del	-/CACACACACACACG			intron-variant	PHF21A	GRCh38.p7	11:46040922	ACACACACACACACA[-/CACACACACACACG]CACGCACAATTAAGG	51317
rs150161686	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46091087	AGGATTAACTAGTTC[A/C]AGTGCCTCCATTAAA	51317
rs150178295	snp	C/T	0.0279526	0.114869	intron-variant	PHF21A	GRCh38.p7	11:46033566	ACCATGCTTAGCCCA[C/T]TTTCTGTTATTATTA	51317
rs150179334	snp	A/G	9.7028e-05	0.00696452	intron-variant	PHF21A	GRCh38.p7	11:45935539	TAAACAGAAGGACCC[A/G]AAACAGCCTGGGGCC	51317
rs150184344	snp	C/T	0.0174175	0.0916809	intron-variant	PHF21A	GRCh38.p7	11:46117472	CTCAGTCTTTGCAGG[C/T]TAACTTAAGTACATC	51317
rs150213753	in-del	-/AAGGCCA	0.021333	0.101051	intron-variant	PHF21A	GRCh38.p7	11:46012769	AAATCTGGCCTGCTT[-/AAGGCCA]AACTCATTGTCTTCC	51317
rs150224569	snp	A/G	8.24002e-05	0.0064182	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979955	CTTCCGTAGCTGTTC[A/G]ACTACTCTTTTCTAC	51317
rs150231324	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026537	GAAAGCTTTAGCTAC[C/T]TCTTCTCTACCCTGT	51317
rs150235608	snp	C/G	0.0103295	0.0711199	intron-variant	PHF21A	GRCh38.p7	11:45966041	ACTCCTCCTCTCAGT[C/G]TCCTTTGTGGGCTTA	51317
rs150265682	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053275	AATATCAATATGAAA[G/T]AATTATTAGTGAAAC	51317
rs150297594	in-del	-/A	0.0146672	0.084371	intron-variant	PHF21A	GRCh38.p7	11:45970024	ACAAGCTTTCATCGT[-/A]AGTTAATCATCTGAA	51317
rs150319005	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46045725	ATCTGTTCTCTAAAA[C/T]ACGTAGGTTACTAGA	51317
rs150331614	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990601	CTAAGTACTGAAGCT[A/G]TGATTCATGCTTTTA	51317
rs150340926	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929659	TGGGGAAGGGGTAGG[A/G]GGGTGGGGTCCTCAG	51317
rs150383513	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45983484	GTTATACATGTCTGT[C/T]GCTATCTGTGAAAAA	51317
rs150386291	snp	A/G	0.0174175	0.0916809	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084941	CATCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA	51317
rs150395204	snp	C/G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46060870	CTTTTGCACCTTCAT[C/G/T]GTGAAATCTGTGCCC	51317
rs150425973	snp	A/T	0.000115412	0.00759556	missense, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934176	TTCTCCAGGGAGCTG[A/T]GCATCTCCTTCTGCC	51317
rs150440208	snp	C/T	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46076339	AACCTACATTTAGAG[C/T]AATCTACTTACAAGA	51317
rs150457423	snp	C/T	0.0150606	0.0854603	intron-variant	PHF21A	GRCh38.p7	11:45962556	AGGCTGCCCAGCAAA[C/T]TAAAATAACAATGAC	51317
rs150501546	snp	A/G	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:46022971	GGCCAGGCTGGTCTC[A/G]AACTCCTGATCTCAG	51317
rs150537895	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079733	GGAAGTGCAGGAACA[A/G]TACAAAACTCTATCT	51317
rs150586830	in-del	-/A	0.0263992	0.111815	intron-variant	PHF21A	GRCh38.p7	11:45991960	ATGATTACATTTTGC[-/A]AGACATGTAATAGGA	51317
rs150618234	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959647	AAAAAACTCAAAGAA[C/T]CCATAAAACAAATAC	51317
rs150639079	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46103636	TGGGTTAGTGAGAAC[A/G]AAAAGTTAATAGGAG	51317
rs150642561	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042871	TGCTGATGCCTTGAA[C/T]GTGGACATCCCAGCC	51317
rs150695006	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036066	TAATGGCATGGGCTA[A/C]AGTAGTGCTTATGGA	51317
rs150702606	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975367	TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAC	51317
rs150727247	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46122970	ATAGTGTTGGCCTTC[G/T]AATGTTAAATAACAA	51317
rs150763047	snp	C/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46067762	TTCTAGACTTGAGGG[C/G]TACAAATGTGAGCAA	51317
rs150791694	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46074455	ATAAGTGGCTCTTTT[-/G]GGCGGGAGGGGGGAA	51317
rs150848173	in-del	-/ATCT	0.272693	0.248968	intron-variant	PHF21A	GRCh38.p7	11:46015896	TGCTGTTTTACAGTC[-/ATCT]ATCTATCTATCTATC	51317
rs150871012	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932722	TAATTTAAAAAAAAG[C/T]TTTTTTTCCCCAGAT	51317
rs150902436	snp	A/T	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:46003202	AAGAAAATCTGTATA[A/T]GAGAGTGCCACTAAA	51317
rs150905645	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46088240	ACCATCAGACTCACA[A/G]GACAGTAACACACTG	51317
rs150954424	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050347	AGTGGCCGGCTTACT[C/T]TGATCAACTGAGTGG	51317
rs150956438	snp	A/G	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46012152	CTGCCTGAAGTTCAT[A/G]CCATCTTTACCCTAA	51317
rs151009796	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006787	CAATAAAAATGGCAC[A/T]AAAATATTTTAAGAC	51317
rs151015262	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46090539	AGATTCACAATGCAC[A/C]TTAGCATATTAAAGG	51317
rs151015910	snp	C/T	0.0429648	0.14013	intron-variant	PHF21A	GRCh38.p7	11:45989796	TTGGGCCCAGGAGTT[C/T]GAGACCAGCCTGGGC	51317
rs151038480	snp	C/T	1.64841e-05	0.00287085	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979829	GTGGTACTGCTGCTG[C/T]TGTTGTAGTTGCTGT	51317
rs151045696	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46025862	GGTGATGGGCTGTGA[C/T]TGCTCATAGCCCATT	51317
rs151069410	snp	A/G	0.00914312	0.0669923	intron-variant	PHF21A	GRCh38.p7	11:46083384	AGATATTCTCCCAAC[A/G]ATTTCAAAAGTTAAT	51317
rs151072512	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45946169	AGGAAGGAAGAGAAG[C/T]AAAGATTTAAATGTC	51317
rs151078594	in-del	-/ACAC			intron-variant	PHF21A	GRCh38.p7	11:46099524	CTATAGAAAAATTAG[-/ACAC]ACACACACACACACA	51317
rs151079931	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018413	CAGTATAGTATTAAC[A/G]CTTAGCCTCTGGTGT	51317
rs151090965	snp	C/G/T	0.000182869	0.00956065	missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934057	TGGCGGCATTGGCAG[C/G/T]GGGGGTGCAGTCCGG	51317
rs151158619	snp	A/G	0.0130921	0.0798413	intron-variant	PHF21A	GRCh38.p7	11:46107528	CTGCTACATTCTACC[A/G]GGTCCAATTCTTAGA	51317
rs151169176	snp	A/T	0.0137019	0.0816284	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965540	CTGGATAAGCTGAGG[A/T]GCTGCGAGCATGGGA	51317
rs151205906	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45982921	ACTATACCAGTCACA[A/G]AAGGAAAGGGTGTTT	51317
rs151220439	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46056602	AAGAAATCTAAACTC[A/G]TTCAAGATAGACAAT	51317
rs151221058	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45961438	CCAGTATTAAAATGG[A/G]GTAAGGGGAGGCATC	51317
rs151228359	snp	A/T	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:46038363	GAACTCCTGACCTCA[A/T]GTGATCCACCCGCCT	51317
rs151237777	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45976223	GCTCTTTCCCCTTTG[C/T]TCTATCACTAAAATC	51317
rs151253135	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45940345	GGATTACAGGCGCCC[A/C]CCACCACGCCTGACT	51317
rs151256197	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075978	TTTTGATTAATATAT[G/T]CACCTACTCCAAGAC	51317
rs151279777	in-del	-/TCT			cds-indel, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930972	TGGGTGCCAGGGGCC[-/TCT]TCTTTACAGTAAAGC	51317
rs151309055	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46069770	ATCTCAGTTTATGTA[G/T]CACAATGATGCACTT	51317
rs180739118	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45948276	CTGCTCTGCCTAAGA[A/G]TAAGATTCTGGAATG	51317
rs180743572	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45974253	TTAGATCTTTACCCC[C/T]ACTCTGGTGCTTCTT	51317
rs180750369	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46007841	TTTCAAATTTTAGAA[C/T]AAGGGACTTTTCCAT	51317
rs180753063	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45996929	GCACAAATGTATCCA[C/T]TGTAAATGTTAGTCT	51317
rs180788005	snp	A/G	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:46015392	TACAATTACTTTTGA[A/G]GACTTAGCCATAAAT	51317
rs180797007	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038137	CTCTCTCTTTTTTTT[C/T]TTAAATGGAGTTTTG	51317
rs180886193	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46116413	CTTGAACCATGACAT[A/C]TGTTACTCTGTCAAT	51317
rs180909664	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46092636	TCCTCATAAAAGGCA[C/T]TTTTTTCAATTAATC	51317
rs180913920	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46069860	AGATGAAAGTGTTAC[A/G]TATGAGATGAAGTTA	51317
rs180922435	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46048997	CAGAAGGGAGACTAT[G/T]AACTAGCTGTCTGTT	51317
rs180928629	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46027337	GTTTACCTTATTTAT[A/G]CATGTATAAGGGGTT	51317
rs180944051	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46103893	ATAGAGACATTCGTA[A/G]GACAGATACATATAT	51317
rs180962152	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46058012	TGCAAACGTTTTTCC[A/G]TCAGTTAAGTTTCCA	51317
rs180993881	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46080528	ATGATTATATTAATA[C/T]ACTAAACTATAAACA	51317
rs181036905	snp	C/T			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123405	ATGGACTTTATGGTA[C/T]ATGTGTAGGCCATTT	51317
rs181043186	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46097499	AATTATTGAGGAAAT[C/T]TACAGCAGTTTCAGG	51317
rs181045463	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46073253	GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC	51317
rs181049397	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053183	TGATAAATGTTTGGT[C/T]TCACAGAACACTAGA	51317
rs181056169	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46030498	AGATCCAAAAAGAGA[C/T]AACAAGGAAAGTATT	51317
rs181091821	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46063495	AAATGTAAAGAGTGT[C/G]ATTGTGTTCTAATAA	51317
rs181153964	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46011045	CATCTGCTTAATTAT[A/G]GTTCCCTTTCCCCTT	51317
rs181175786	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929142	GGCACTCTGGGGCTA[A/G]GGCGTCAGTGCACAA	51317
rs181182379	snp	G/T			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123021	ATACAAATGGGGGGG[G/T]GGGGGGTTTTGTTTT	51317
rs181189621	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46069519	AGGCTGGAGATAGTC[A/T]TATATCAGGTAACCA	51317
rs181205426	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960780	TGGTCTCTGAGATTA[G/T]AAACCATGATGCAGA	51317
rs181210071	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987857	CATGGCTGTATCCCA[C/T]AACCTAAAGGCAGCA	51317
rs181218749	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007630	CCATCTATCTTTTAT[G/T]ATAGTTTTACTGTTA	51317
rs181222709	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967884	AAACTTTCTGAAATA[C/G]AGAACACAGTATGTG	51317
rs181232204	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943222	CAGCCTCCCATGCTC[A/C]AGTGATCCTCCCACC	51317
rs181243894	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45991653	GCTGTAAAAATAATA[C/T]ACTGGGTCGAGAAAC	51317
rs181273566	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46087954	TAGTGACAGGGTTTC[A/G]CCATGTTGCCTAGGC	51317
rs181360844	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45937485	GTTGTTTTATTATTA[G/T]TATTATTTTTTTGAG	51317
rs181363705	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46111114	TAAATCACAACTATG[C/T]GGGGGGGGAGGCTAG	51317
rs181405555	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941819	TGTTTTTAGGAAGCA[C/T]TCTGGCAATACCAAC	51317
rs181406324	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46115759	AGAGACCTAAAACTT[C/T]AATTCCTTCCCTTCT	51317
rs181409485	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45967613	TTACACCTGAGCTAT[A/C]CTTGGACAGCTGTAG	51317
rs181418608	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46048934	TGGCTGTAACATTTT[A/T]CATTCCCACCAGCAA	51317
rs181419763	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991208	GTTTTTCATGGTTTG[A/G]TAGTTCATTTCTTTT	51317
rs181424532	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068832	CTTACAAGAGGATTG[C/T]TCTGCCTTAACTCAG	51317
rs181429800	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46010803	CCCTGACTAACTCTA[C/T]ACCCCTACCCAGTGG	51317
rs181439770	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46026862	AAGGCCTTACATCTT[C/T]AAATGCCTGGCCCAC	51317
rs181443157	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45947050	CATCCTGATAAACTA[C/T]ATCTCTAAAAATTGG	51317
rs181465065	snp	C/G	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:45995670	AAGGCTCTACAGAGT[C/G]TGCAAGACCAGCACA	51317
rs181470648	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46030380	TATTCTTACCAAATG[A/C]TTTGCCCAGGTTTTC	51317
rs181516764	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930827	GTGGGGAAAGAGCAG[C/T]GGAGGGAAGGAGGAG	51317
rs181536064	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45981279	TAATCCCAGCTACTC[A/G]GCAGGCTGAGGCAGG	51317
rs181557749	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092438	AAATTGCTACTTTTC[C/T]ATAGTTTTTCAAGAC	51317
rs181566461	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46048422	TCCATCAGTTTATGG[G/T]TTGTTTCCACTTTTT	51317
rs181591588	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973971	TCTACAAAATACTGA[C/T]TAAAGCCTCAAACTC	51317
rs181620004	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46017578	AGGATTTGCCCTTAA[A/G]GGGGAAAAAAAAAAA	51317
rs181627396	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022226	GGGAGGCCAAGGTGG[C/G]AGGACCACTTGAGAT	51317
rs181646403	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052638	AGAAGAAAGATATTC[A/G]TGAAGCTAAATTGCT	51317
rs181660086	snp	C/T	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46109850	CCGGGTGTGGTGGCA[C/T]ATGCCTGTAGTCCCA	51317
rs181663065	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087506	AAGTTAGGACTAGTT[C/G]TAGAAAAACATATGA	51317
rs181666044	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46062795	AAACACACCTACTAT[A/G]CAACCCAGACATACT	51317
rs181670164	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45953231	AGCTGGGAAAATCAT[C/T]GCTCATCTTAACATT	51317
rs181698168	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46002776	CCTCAAACCCCTCCA[C/T]AGAACTAGTTTTATC	51317
rs181715489	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46072881	TTCGGAATGTTAAGA[C/T]TGCCTCTACAAGAAA	51317
rs181775441	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059161	AGGAAATAATCAAAA[C/T]TACGTACAAATATTT	51317
rs181777392	snp	C/T	6.81733e-05	0.00583798	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935734	TCTGTTTCTCTTCTT[C/T]TTTTGCTAAAAAAAA	51317
rs181778635	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46092082	CCCATTTCTGAGAGA[C/G]AGCCTATTTGCCAAA	51317
rs181780211	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46115215	CAAGTCTAGTGTAAG[A/G]AAGTTGCTTTAGAAG	51317
rs181783081	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039105	GGGGTCTGACAGACA[A/C]CTCTAAAGACTTGAC	51317
rs181798529	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015545	TTGCTTTATAAAGTT[G/T]AATTTTTAAACTTTT	51317
rs181798557	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068354	AAAAGGGAATAAATG[C/G]GAATGGATTTTTTGA	51317
rs181820915	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45968958	AAAAAAAAAAAAAAA[A/T]AGGCAGGTATCCCTC	51317
rs181882731	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45948653	CTACATTAAGCCATT[C/T]CCCTGAGTCAGCTTT	51317
rs181888920	snp	A/C	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:45975319	ACCCTGTCTCAAAGA[A/C]AACAAAATAAAATAA	51317
rs181892368	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998044	ATCAGTAGCAATCAG[C/T]CTGCTACCCAGGAAT	51317
rs181923782	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46081314	AACAATACATATTCC[A/G]AGAGTTTAAAGGGGA	51317
rs181924410	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45943451	TCCCAAAGTGTTGGG[A/T]TTTACAGGCGTGAGC	51317
rs181928955	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46001508	TCTCCGTCACATGCA[A/C]CACAGCATCAACAGA	51317
rs181949950	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46047397	CTGGTAAGGTATTTT[A/G]TAATTTTTTTTTATT	51317
rs182016257	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45959177	GGTATCTCAACTGGT[A/G]TAGAAAAAGCATTTG	51317
rs182020662	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46099556	CACACACACACACAC[A/C]CACACACCCTAAACA	51317
rs182037599	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007134	CAACCATAACGTGAC[A/G]AGACATCTATCAACA	51317
rs182047502	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46063832	TACTGTTTCATCTGA[C/T]GAACCCACATCATAG	51317
rs182051392	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45936915	ATCAGCATGATGGCA[C/G]CAGCCACTGGCAGTT	51317
rs182052056	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46086725	TTTGAAGTTGAAGGT[G/T]TATTTTTCAAATATT	51317
rs182054401	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062522	CCTCTCCTTGTTTCA[C/T]TAATGCAATATCTTC	51317
rs182062674	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46043247	CCTATCAATGATCCT[A/G]TTCTATCCAAGGACT	51317
rs182073647	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043608	AGGCAGTATTAACAC[A/G]TTACAAAGTGCCAAA	51317
rs182077352	snp	A/C	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46019930	ATAATCTTAATCATC[A/C]TGTCATCTCATTTCA	51317
rs182085508	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45952588	TAGTACTTCTTTTTG[G/T]CTTAAGTTTTGGTCC	51317
rs182090821	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45980302	AAAAGCAGGACTCTG[A/G]AGCCATCCTACTTCA	51317
rs182103079	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45944029	AAAATAAAGGATTAC[A/C]AAACAGACAATATCA	51317
rs182113813	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988233	ATATAACAGATTATT[C/T]AACCAAATTCTATGC	51317
rs182115466	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949926	ATCAGAAGAGCACTT[C/T]GCTGTGCTGTTCAGA	51317
rs182148362	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45992299	GCACTTTGGGAGGCT[A/G]AGGCGGGCAGATCAT	51317
rs182201285	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104371	TACTATAAACTGCAT[C/T]AATATCTTGGTGCTG	51317
rs182235745	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46025777	TCTCTGGAATTATTT[A/G]CAAGTCATAGGCATA	51317
rs182253464	snp	A/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46073723	GAGCACATTCCTGTA[A/T]CATTAAAATACTTTC	51317
rs182258111	snp	C/T	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:46108751	TAACACTCTAAAACG[C/T]TGATCGTTATATAAG	51317
rs182289031	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45976215	CTTGTGAAGCTCTTT[C/T]CCCTTTGCTCTATCA	51317
rs182293776	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031072	TACGACAAGCGATCA[C/T]GTAGTAAAAGCTGTG	51317
rs182299431	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935607	TCTGCACCTATGTAT[C/T]GACTGCTGAAGGCAT	51317
rs182317494	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987310	TCAAAGACCCTAGAC[A/G]CAGTAAATACCTAAG	51317
rs182318788	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46118476	AGCCAGATGTTTGTG[C/T]TTTGAGAACTTTGTG	51317
rs182407404	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970153	AACATAGCAGGCTCA[A/G]TAAATCTTAGACAAT	51317
rs182421231	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46049562	GCGGGGGAAGGAGGG[A/G]TAGAAAGAGGATAGG	51317
rs182440893	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938050	ATGCAGCCCGGAGAC[A/G]GACTGGGAGAGAGAA	51317
rs182477810	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932069	CAGAGCGAAGGCCAC[A/G]CTGGGGCTCTGTCTC	51317
rs182485583	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45954348	AACCTGCTTAAGATC[A/C]GAATGATGTTAAAAA	51317
rs182490297	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982618	CATGTAAATTTTATT[A/G]CTTGGTGACTGCTAG	51317
rs182499847	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46003572	ATGATGACATTTTCA[A/C]GAAGGGCAGAGTGAG	51317
rs182523856	snp	A/C	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46098342	CTATATGCTTGAAAA[A/C]TGTGAGCCACACTAG	51317
rs182525415	snp	G/T			missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965353	TAAGCTGTACAGTTT[G/T]AGGTCCAGCGAGTCT	51317
rs182551157	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46053713	CCTCATCTTCCTCCC[A/G]TTCTTCTTCCTGGTT	51317
rs182568631	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46012107	CTGTTCATTACTACC[A/G]GAAAGAATCCTTCAA	51317
rs182590564	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929541	CTCTTCTCTGCTAGG[A/G]GCTGGCTGACCTCTG	51317
rs182613060	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931276	GAAAAGGTAAGTTAG[A/G]TGTTGTGTGGCAACC	51317
rs182614957	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105477	TTCTCCACACTCAGA[A/C]CCACACTAACCAGGA	51317
rs182632943	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46059555	CTCAGCTTCCCAAGT[A/G]GCTGGGACTACACAC	51317
rs182644733	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016672	CTGCAATTTGTAGCT[C/T]ATGTTTTTCTCCTCT	51317
rs182656431	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46100265	GGCTTCCATTAACCT[C/T]GTTTAAAAAAAAAAA	51317
rs182668205	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075346	CACTAATCAGTTCTC[A/T]CCTTCTTCCCCTGCT	51317
rs182674816	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46055128	TTTTAAATTATGGCG[A/G]GAACTTAAGATACTT	51317
rs182677662	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46032304	CCCAGAAATAAGCTC[C/T]GTTATTTCTTTCTAA	51317
rs182702365	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45963551	TTACGGGGAAAAGCA[C/T]CTTCTACAATTTATA	51317
rs182704551	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100874	ATAGCAAGTTTCTAA[A/C]CACTGTTACCACGTC	51317
rs182709968	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45939826	TCTTTTCCAGAGAGT[C/G]AATGCCTAGCTCATT	51317
rs182714947	snp	C/T	0.00208187	0.0321963	intron-variant	PHF21A	GRCh38.p7	11:45965301	CCCAGAGCAGGTACA[C/T]ACTCTGCCTGTACCT	51317
rs182722540	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45988924	TCTAAAGCTGCTGAA[G/T]GCTACCCTCTTAGTT	51317
rs182727342	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009490	CATCTAAACATGTAA[C/T]GATAATAGCAGCTGC	51317
rs182780921	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46013315	TCTCTCCCTGTCCCA[C/T]CCCTTCCTACCCAGA	51317
rs182786102	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46043798	TGTCATATACCCACA[C/T]TGAAATGAATGCTCA	51317
rs182788459	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46104700	AGAGCAGCTATCATG[A/G]TTGAGTGTCTCAAGA	51317
rs182790040	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46082758	TGGTATGCTTGAATT[A/C]AGAATATGAAACAAA	51317
rs182794799	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028723	GGATTACAGGCGCCC[A/G]CCACCACGCCCAGCT	51317
rs182802176	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46059240	TGGGAATAATTTAAA[C/T]GTCTAAAAATAGTGA	51317
rs182807079	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039456	GGAAGCCTGAGAATA[A/G]TCAGGTAAGTACAGG	51317
rs182874361	snp	A/G/T			intron-variant	PHF21A	GRCh38.p7	11:46049856	TTCCTAAAAACAACG[A/G/T]TAAGACTATCCAGCA	51317
rs182894062	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46083985	AGTCAGGAATACTTT[A/G]AGTTCTTAAAAGCAG	51317
rs182913622	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112133	TAGTCAAAATATTCA[A/G]TTACTGGTGTGATAG	51317
rs182914470	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040485	GTGGGGAGGGGTGAC[A/G]GCTTGGGGCTCTGTA	51317
rs182922109	snp	A/G	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46089232	TTTACTTCTTGTACC[A/G]TGCTTAATATTTGAA	51317
rs182930796	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944772	ATCCATTCCATTTTT[G/T]ATCTCTTTTTAGAGA	51317
rs182942592	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970839	AAATGAAACAGTGTG[C/T]ATGCCTCTGTGAAGG	51317
rs182962836	snp	A/G	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:45998984	GGCACCTGCCACCAC[A/G]CCTGGCTAATTTTTA	51317
rs182969112	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972058	CCAGTTCTTGATACT[A/G]AAGGGATATTATGAG	51317
rs183018182	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949323	GCTGCTCTTCAGCAG[A/G]TTTTCAGAGGGGAGG	51317
rs183041770	snp	A/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45998403	AATATGCCTACTGAG[A/T]ATATAGTATTGTAAC	51317
rs183086827	snp	A/G	0	0	intron-variant	PHF21A	GRCh38.p7	11:46022766	TGATCCACTGTGCCC[A/G]GCTCATATACTGTTA	51317
rs183093713	snp	C/T	0.0119091	0.0762411	intron-variant	PHF21A	GRCh38.p7	11:46054198	AAGAATTTCAACCAA[C/T]TCATTTAAAAAAATT	51317
rs183101819	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46032104	CTCAAAAGGAGACAC[A/T]CCAGAGTTTGATTTA	51317
rs183110833	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46012933	TCCTGCTGCTGTACT[A/T]CAGTCCTCATAGGGG	51317
rs183122641	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070772	ATTTAAAACCAAAAG[A/G]TAATTTATGGAATAC	51317
rs183123522	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45992701	ACAAAAGGCAAGTTA[C/T]ATGAATGAGTTCTGA	51317
rs183172597	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45974927	AAATACATGGCATGG[A/C]AAATACTGCCAATAG	51317
rs183198309	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46106666	TACAACCACTTGTAC[C/T]TAACATGCATGCTGC	51317
rs183213772	snp	A/G	0.0146672	0.084371	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084374	TGTTAAATAAATTAT[A/G]TTAGTAAAAGAATAT	51317
rs183214589	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46060731	TAGACCTTTGTCAGA[G/T]GCACAGTTTGCAAAC	51317
rs183221783	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46117244	TTTCTAGCATCCCCA[A/T]ATTTTTAAAACTTCG	51317
rs183225167	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041518	TTCATCTTGGTTTCA[A/G]TTATAGCCAGGCCAA	51317
rs183232442	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45999232	GAAAACAGGACCACA[A/C]ACAGAGGTCAAGATC	51317
rs183240919	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946452	GCTGTGGCACGATCT[C/T]GGCTCACTGCAACCT	51317
rs183259824	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994042	AGGGCAGCTGAGCAG[A/G]GATAAATGCTGGAGC	51317
rs183277474	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983954	TGTTTTAAATGAAGA[C/T]GTCATGACTGCTGCT	51317
rs183281727	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46003947	TTTGGAAATACATCT[C/T]TATGAAAATATGTAT	51317
rs183296617	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45976060	AACCCAGAAGCTCTG[A/G]CATGCTTTGGAGGGC	51317
rs183320866	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46117396	ATATTCATCTTTATG[A/C]AGTTACTGTTACATC	51317
rs183370084	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094363	TAGAAAATCAAACCC[A/G]GAAAAGTTAAGTGAT	51317
rs183374064	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46111305	TGAAACCCCATCTCT[A/G]CTAAAAATATAACAA	51317
rs183386217	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088829	CTCAAATTCTCTAAG[G/T]AGGTTCTTCTAACTA	51317
rs183393208	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050283	AGTGTCCTTGCTCAC[A/G]GCAGGAGAAAGGCAT	51317
rs183397907	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46064556	ATTTTGCAGGACAGC[C/T]TCCCATCTAACCAGC	51317
rs183402691	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044239	TGTCCTATAGTACAG[C/G]TAGAGGTACCTTTTG	51317
rs183411100	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023663	ATGTGTGTTAAGAAT[C/T]ACTGAATGGAGGCCA	51317
rs183424234	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015844	GGTAACAATGCCTTC[A/G]TCTGAAATACCTCCT	51317
rs183485406	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46064742	TATTAATATCAACAA[C/T]GATAATGATAGTTTA	51317
rs183488551	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46099720	ATCCACATTTCAAGC[A/G]CTAAAAGAATTAACA	51317
rs183497945	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46023854	CCAGCTACTCAGGAG[C/G]CTAAGGCAGGAAAAT	51317
rs183541088	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933815	AATTGGCAAACTCTG[A/G]TGCCACCTGGCACAA	51317
rs183558667	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984383	GATTCCCTTGACATT[C/T]GCATCACTGGGTTTC	51317
rs183640689	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46049718	GGGGGTCCCCTCCAC[A/G]TTCCATATTGTAAAC	51317
rs183667120	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114741	TCAACTACTGTTTGA[A/T]TTGTAAGTATGTCGC	51317
rs183677224	snp	A/G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46090433	CTAAGGATAAGAGTC[A/G/T]TACAAAAAAGGAATG	51317
rs183682025	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46067917	GAGGAGTGTCTAACT[A/C]TGCTTGGAAGGTAGA	51317
rs183689228	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46046273	ACAGGACAGTGCCAA[C/T]AGCACTGGGGCCATC	51317
rs183728450	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045059	GAAAAGTGTTAAACA[C/T]ACAGCAAAGTTCTTA	51317
rs183731776	snp	C/T	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:46074691	TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCACGT	51317
rs183738877	snp	A/T			missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979899	TGTGGCAATGGCTGT[A/T]TTTGGAACTTGTCCG	51317
rs183776009	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45956952	ACACAAAAAGGTTGA[A/G]AGTGAAAGGATGTTT	51317
rs183794952	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004569	GACAGAATATTCTCT[A/G]TTCTTTTCTTCAACA	51317
rs183824040	snp	A/G	0.0119091	0.0762411	intron-variant	PHF21A	GRCh38.p7	11:46094673	GGATCACGAGATCAG[A/G]AGATCGAGACCGTCC	51317
rs183825077	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45964615	CCAAATTCTTCTTTC[C/T]CATCACTAGTCGTTT	51317
rs183828950	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071258	ACTACAAAATGAATA[C/T]GCCCCAGGTAGCTGC	51317
rs183832051	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46051463	CACAAAAGAGTTTAC[C/T]AGGCCTTCATTTCCA	51317
rs183842706	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46029071	CCTTTTCAAAACAAA[A/G]TGTAGCTTGCAAAAG	51317
rs183844395	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46008497	GAGAAGTGCCAATGT[C/T]TTGAAAGCTACTCCA	51317
rs183850086	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46093551	AATTTTAATCACCAA[A/G]GTTAGGATGACTCTC	51317
rs183866845	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46027563	ATTTGATTCAGTCTT[C/T]AATGCACACAACTCT	51317
rs183908133	snp	G/T			missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935739	TTCTCTTCTTCTTTT[G/T]CTAAAAAAAAAAAAA	51317
rs183911508	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929279	GGACTGGAATGTGTC[C/T]TGCCCACCCTCCCCT	51317
rs183914141	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955175	TTTTTGCATCCCTTT[A/G]TGCCTATTATGGTAC	51317
rs183917223	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45952488	CTTTGATAGGGAAAT[C/T]TTGCTCAATTTTTCC	51317
rs183917955	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102193	AGCTCAAGTGATACA[A/C]CAGCCTCGGCCTCCC	51317
rs183922127	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46010117	AGTTTGAGAGTTACT[A/G]CAGGAATGAGAACAA	51317
rs183923351	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078486	AATTATCAGAAGACA[A/T]GGTAAGTTTTTAGGA	51317
rs183925297	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45979407	GCTAAGAATTCCAGA[A/G]GAGGTCAAGTCACAA	51317
rs183933276	snp	A/T	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:46000928	TCCGTCTCAAAAAAA[A/T]AAATAAATAAATAAA	51317
rs183943587	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057582	AAAGAGAGTTGGTAT[C/T]TCTTTTAAAATGTCA	51317
rs183979766	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005688	TAAACATTAGGGGAA[C/T]CATCAGCACCAACTA	51317
rs183999088	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075695	TATAAAGCAGTTGTT[A/C]ACTCAGCTTGGAAGA	51317
rs184007414	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938825	TTCAGATAAGGGGGA[A/G]ACTAGTGTATTCTTT	51317
rs184018751	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46033135	TCATGAAATTCTCCA[G/T]GTTGATACATATACC	51317
rs184022149	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45988338	AGTTTTCTTAGAAGA[C/T]AGAAAAAGACAATAA	51317
rs184049603	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070629	AGCCACCGCACCCAG[C/G]CTGGTGACTATAATT	51317
rs184054404	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45941844	ACCAACTGCAATTTC[A/G]TCATGTGCTAAACAA	51317
rs184065713	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967763	TCGGTATGAATGTCT[A/G]ACTGAACTTAAAACG	51317
rs184069029	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45991332	CTGTTACATAAAAAC[A/G]AAGTAATAATATCAG	51317
rs184070115	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933582	AAGTAAGGATCTGAA[A/T]CCTGCTCTCCTCCCT	51317
rs184079599	snp	A/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46010907	CAGCATCATACCAGC[A/T]CCTTTCTCTCCTACT	51317
rs184146798	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46065736	TCCTTTTCTTTAACA[A/G]AAGTTGTTTAAGCGC	51317
rs184149212	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45934270	GAGCCGCCTGGTTTC[C/T]AACAGGCCTGGCAGC	51317
rs184153968	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46024248	CTTCTCTGACTTTCC[C/T]ATTTCTCCCACTTAC	51317
rs184161376	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958289	AAAGACACCAAAGAA[C/T]AGAAAATGGGCTGGG	51317
rs184162426	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055650	ACCAAGTCTATACAT[C/T]ACATCATCAAAGGAA	51317
rs184174793	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985708	TTAGACAAATAGTTT[A/C/T]TTTCCCTTTTTAACC	51317
rs184226295	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46073189	AAAAATTGGCCAGGC[A/G]TGGTGGCGGGCGCCT	51317
rs184234709	snp	A/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46052649	ATTCATGAAGCTAAA[A/T]TGCTCCTAGCTGCTA	51317
rs184240080	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46107917	TAGTGGTTGAGTGAG[C/T]AGGGATAGGTGATGG	51317
rs184241947	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46030469	TATCAGATTTCAATA[A/C]CAGCATTTTAAAAAG	51317
rs184242670	snp	A/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085221	TATGATGTGGATATT[A/T]TAAAATGTATCTATC	51317
rs184245621	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46061600	TCCAAAGAAACTATA[A/C]AATGTCTCTCAATAA	51317
rs184354468	snp	A/C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46077725	CCTGTTGTCCAACAA[A/C/G]TTACTGTCCTGCCTA	51317
rs184358292	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46108569	AATGTGTGTGTGTGT[A/G]TATATATATATATAT	51317
rs184361250	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056499	TTTTAAAACAAGAAA[C/T]TGGGCTTTTAAAAAA	51317
rs184370844	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46035690	TTTTACACTGAGACT[C/T]GAAGGATGTGTATGA	51317
rs184371544	snp	G/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46062093	CTGTTTTTTGTTTTG[G/T]TTTTTTTTTTCCTCT	51317
rs184379043	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46014428	TGATGGACACCTAGG[C/T]TGATTCCATGTCTTT	51317
rs184385276	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46019588	GTTCTTTCTGATGCT[A/T]TAAATTGCACTCTAT	51317
rs184450984	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946846	AGACCGGCAAAGCAA[A/G]GAGGCAAAATTCAAG	51317
rs184453159	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45973302	TGAAAAGTACCTCCA[C/T]TCTTTCAGAAACACA	51317
rs184462546	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994867	TCACACGCTTTGAAT[A/G]TCTCCCTGGTATTTC	51317
rs184467859	snp	A/T	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:45940434	CTCCTGACCTCATGA[A/T]CTGCCCACCTCGGCC	51317
rs184480690	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45990284	TTTTTTTTCAAACAG[G/T]ATCTCACTCTGTCCC	51317
rs184484640	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46086658	AATTTTTACAAGGCT[A/C]TACCAGAAAATGTGT	51317
rs184502334	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46042481	GACTAAAATCACTGA[A/G]TGGTTTTTATAAATC	51317
rs184563278	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973990	AGCCTCAAACTCACC[C/T]GAATTATATACTTAC	51317
rs184573590	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46030820	TAGTGTGTGTGTGTG[C/T]GTGTGTGTGCGTGTG	51317
rs184605261	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45966548	CAAATCCTAGTTCTA[C/T]CACTCACTAGCTGTG	51317
rs184606108	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042238	ATGACAAAACATATT[C/T]CTCAATAAGGCATAT	51317
rs184683899	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45947255	GCCCTTGTCTTCTAG[A/G]GGCAAGGTCATTGCT	51317
rs184689881	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45950552	AAAATCGCAAAAAAA[A/C]CTCATGATGTTTTAA	51317
rs184697579	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45941166	TGCAGTGCTGTGATC[C/T]TGGCTTACTGCAGCC	51317
rs184707264	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089666	CTAGTTGGATGTTTC[C/T]ATACTATTAAATTAT	51317
rs184719575	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46115236	GCTTTAGAAGAGTCC[A/G]AAGGATGGCTGAACC	51317
rs184732938	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045489	CTACTATTACTCCAG[G/T]CTAATTACTTGCTAT	51317
rs184751694	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45946675	CCACCGCACCTGGCC[A/G]AATTTATTATTTTTT	51317
rs184757143	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45972175	GAGTTTTAAAAGCCT[A/G]AGAGATCAGAAGATG	51317
rs184828216	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113173	GCTCTAATCTGAAGT[G/T]AAGCAAAAACTGCAA	51317
rs184830748	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46108899	CCCACCCCATGCTAC[A/G]CACTATGCTTGGCAA	51317
rs184835297	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45951677	GTGTGTGGACTGATA[C/T]TCAGATGCACCCTCT	51317
rs184838873	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46086760	CTTCATTCTACTGAC[A/G]GTAACATAAAACCAT	51317
rs184844524	snp	G/T			missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46076786	CTGTGATTTTGGCTT[G/T]GAGTTCATGAAGCTG	51317
rs184848700	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46037680	AGGGTGCTTATCTGA[C/T]TCTTATCCTTTTGTA	51317
rs184850381	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46066524	GCAACAAAATGAGAA[C/T]CTGTTTCTAAAAAAA	51317
rs184885017	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46042019	GTGTTAAAAATGGCA[A/G]TTTTCCTACTATACT	51317
rs184918284	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46116488	CAACTACTATCACAT[C/T]ACATCAATGGAGAAA	51317
rs184924550	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46093332	TCATTGCCTCAGGGA[A/C]TATTTCAAAAGAGCT	51317
rs184926431	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46070157	CTATAGATCAGAAAC[A/G]TAACTAGTTATAGGA	51317
rs184934119	snp	A/C	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46049454	ATTCCTGTACAGTGG[A/C]ATCTGCAAGCCAAAT	51317
rs184948194	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46027348	TTATACATGTATAAG[A/G]GGTTTAACAGGTTTG	51317
rs184951014	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45978428	ACTGCCAGTATACAG[C/T]AACCTCTATTAAATG	51317
rs184999881	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46007021	CAGTTTTAATCTTTA[A/G]AGCGTTCCTGCAAGC	51317
rs185000843	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46018963	CGTAAGCAGCAAGAA[C/T]ACACACATCATGTAA	51317
rs185014024	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024822	AGAAAGAAAGAAAGA[A/C]AGACTTAGGGACTTC	51317
rs185025534	snp	G/T	0.00795532	0.062565	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PHF21A	GRCh38.p7	11:46120948	ACCCTCCTGCTGCTG[G/T]CTGGCTGTCCCCCCT	51317
rs185084377	snp	A/G	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46053303	AACAAATACCTAAAA[A/G]TAAAGGGTACTAACT	51317
rs185089807	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030765	GTTTTTTTTTAATTT[C/G]TAACTTTAAGAAGGT	51317
rs185094810	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45962308	GATACGGGTTTGGTA[A/T]CTGTGAACAGGTGTG	51317
rs185131852	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46079430	CGGGTGACAGTGGCT[C/T]CCGAAAGGAATTTAA	51317
rs185146942	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46097159	TAACTGGCCTCCCCA[A/G]TTCTACCCTAGCCCC	51317
rs185179985	snp	C/T	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46068604	ATTCCACAAACTTGG[C/T]CTTTGATTTGATATT	51317
rs185188165	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101258	AGACATCTTCAGTAA[C/G]TTAAAAGACAAATGA	51317
rs185194730	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025912	ACTTTTATTGTAGGC[A/G]AAGACATTTCAAAAT	51317
rs185216341	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45997532	ATGCTGGTTTCTCAA[C/T]GTCTAGATCCAGTGA	51317
rs185232195	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933181	AAGGGCCAGTGGCCC[A/G]GGCTCTGCTTGTTCT	51317
rs185234831	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45948429	TCTCAAGTGTGGCTA[A/C]CTCTTTCCTTCCTGG	51317
rs185249053	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45954910	TCATTATGCTGGAAA[C/T]ATTTTACTAGATCTG	51317
rs185251151	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46097522	GTTTCAGGAGCAAAA[G/T]AATACTAAAATAAAG	51317
rs185256898	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45982619	ATGTAAATTTTATTG[C/T]TTGGTGACTGCTAGA	51317
rs185259012	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46044030	ACAGCTGTAAATTTG[C/T]TTTTACCTTCATAGA	51317
rs185262756	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46003702	AGTATGGCTCAGCAC[A/G]CTACAGAGCACATGA	51317
rs185264468	snp	A/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46073272	GGCGGAGCTTGCAGT[A/G]AGCCAAGACAGCGCC	51317
rs185266174	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46023087	TATTTAGGCTAAGGT[A/C]TCAGACCTTGAGTGA	51317
rs185293396	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937856	GTTTTAAAACCATAT[A/T]CTTGGTCTGGACCAT	51317
rs185295222	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45961215	TCCTGTTCTTTTTGG[C/T]ATAATAAAAGAATCC	51317
rs185302170	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46047481	CTGGATAAAGAAACC[A/G]AGACAAAAAGGTAAA	51317
rs185308322	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45987889	TGCTTTGTTAATATC[A/G]GAATTGTCTTGGACA	51317
rs185316708	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46007670	ACATTAAAAATAAAC[C/T]GCTAGCATGAATATT	51317
rs185329003	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46112950	TGATAAAAAATACAA[A/T]AAACTAATCTAAGGT	51317
rs185331265	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46059312	ATGATAGGATACTAT[A/C]AAGCCACTAAAAACT	51317
rs185368758	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45967231	ACATTAGCCAGGCAT[A/G]GTGGCACACACTTGT	51317
rs185376348	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119744	CGAACGTGGTCAGGG[A/G]AAAAAAAAAAAAAAG	51317
rs185384972	snp	A/T	0.0119091	0.0762411	intron-variant	PHF21A	GRCh38.p7	11:46010626	TAATACTGCAAGTCA[A/T]CAATCACAAAACAAA	51317
rs185404855	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46048468	TGCTATGAACATCCA[C/T]GTAGAAATTTTTGTT	51317
rs185414332	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026872	ATCTTTAAATGCCTG[C/G]CCCACCAAAGGTCTT	51317
rs185453836	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007172	ACTGCATACCTACCA[G/T]GTGTTCAAAAACATG	51317
rs185482565	snp	C/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46092131	TATTTGAATAACTAT[C/G]CAGCTAGCATCAGGA	51317
rs185499253	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991063	CCCTCACCCTCTGGC[A/G]ACCACTCCTCTTTTT	51317
rs185505052	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46095242	AACTGAGCAGCAAAA[A/G]GCAAGATCTATACAC	51317
rs185522068	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46052055	CAAGGTTGAGATGAT[A/C]CAGGAGTAGCATATG	51317
rs185610516	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46083256	GAACAAGAGTTTAAC[A/G]AGATCCGGAGCAGCA	51317
rs185616333	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45994670	AACAAGATGTCAGGG[G/T]TTTTGCTGTTGCATC	51317
rs185618979	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119459	ACTTCCAGACCTAAA[C/T]AAAGAATATTTCAAC	51317
rs185638613	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46072297	GGCCACATGACTAAG[C/T]TCAGGCCCATGGGAT	51317
rs185661041	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029772	CCAATAGTGCACCTA[A/G]CTTAAAAATAACAAA	51317
rs185746152	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935431	GATGTTACAGAGCTT[A/G]GGTAAGGCACCACCT	51317
rs185766593	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45986257	AATGCAGTTTTCTTA[G/T]TTAATTCACTCATGC	51317
rs185798134	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46105216	CTGCACTAACATTCT[C/T]AACCTCTGTGTTCTA	51317
rs185815883	snp	A/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46013908	CAGTGAATGAGTGGT[A/T]AGTAAATGTGAAAGC	51317
rs185823050	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46080772	TCCTGGGCTTCAGCA[A/G]TCTTCCCACCTTAGC	51317
rs185828616	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45986429	GAAAGAGTGTGGCTG[G/T]TGTACTCAAGAGAGA	51317
rs185833518	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46038229	CCTCCCAGTTTCAAG[C/T]GATTCTCCTGCCTCA	51317
rs185866314	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45963738	ATAGTGTTGTGAAAC[A/G]AGGTTCTGTGGAACA	51317
rs185880006	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46007899	TTTAAAAAGGTACAG[G/T]ATCTATCACAATAAT	51317
rs185926095	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099853	CTCTCTGACTATACA[A/G]GTTTAGCTCCACAAC	51317
rs185928547	snp	A/G	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46074763	CCACCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC	51317
rs185938106	snp	C/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46104052	TGACAATTAAATATA[C/G]AAAGAAAATAACAAC	51317
rs185943929	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46054380	GGAATAAAAATGCTA[C/T]GTCAAATTGGCTTGG	51317
rs185945848	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46110182	GTACATTCATGAGTA[G/T]TATCTTATCTAATCC	51317
rs185959288	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46058934	GACAGCAGAAATGAA[A/G]CAGAAGCAAAGAAAG	51317
rs185973044	snp	C/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46015454	TTCCAAGGTTTTCTT[C/G]TAGGATTCTTATAGT	51317
rs185988671	snp	G/T	1.73183e-05	0.00294259	intron-variant	PHF21A	GRCh38.p7	11:45938353	AAAAAGGACAAAAAA[G/T]GTAAAATTTTAATGT	51317
rs185999760	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988308	GGATACCTTTTAAGA[A/G]TCCTCAACTCTGTAA	51317
rs186002581	snp	G/T	1.64814e-05	0.00287061	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935670	TGTTTCACCTTTTGC[G/T]CTAGTTGTTCTCGTT	51317
rs186082216	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46114661	CCCAAAGTTTTGGGT[A/T]CTTATTTAAAATTTA	51317
rs186082692	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46099560	CACACACACACACAC[A/C]CACCCTAAACACAAA	51317
rs186086565	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46061588	TTTCCCATACTTTCC[A/C]AAGAAACTATACAAT	51317
rs186095562	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46039266	AGTATAGGTAGGGTG[C/G]AGAATTTGTTTCGAT	51317
rs186104098	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46015553	TAAAGTTTAATTTTT[A/G]AACTTTTTGACTCTT	51317
rs186107087	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943308	TTGTATATTTAGTAG[A/T]GACGGGGTTTCACTA	51317
rs186108898	snp	A/G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46111115	AAATCACAACTATGT[A/G/T]GGGGGGGAGGCTAGT	51317
rs186121322	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992183	TTTTCAACCCTCAGA[C/T]GGTAATTACACTCAC	51317
rs186129219	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46063654	ACCCTGAAGTAATGG[C/T]TAAAACCACTTTACC	51317
rs186244319	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967998	CAAGTGGGTCATGAT[C/T]CACTGTTTGAAAAAC	51317
rs186257089	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088183	ATATTTTGACCAATT[A/C]TAACAAGTTATAAAT	51317
rs186259705	snp	G/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46104621	TCTCCAGCTAAATTG[G/T]TCCAAATTTACTCTT	51317
rs186262048	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46059301	ACCCTACCCAAATGA[C/T]AGGATACTATCAAGC	51317
rs186262987	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45975477	CACATCTGTTTTATA[C/T]TATTTTGCTGGTTTA	51317
rs186264288	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011134	ACTCCTTGAGGGAAA[G/T]AATTAACCGTTTTAA	51317
rs186266489	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092512	CATAGAAATGAAATG[C/T]ACCTCATTTAAATAA	51317
rs186269740	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998095	AGAGGCTAAAAAGAT[C/T]ACTGAATCCCAGAGG	51317
rs186273040	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46082410	TCATGATCAACAATC[A/G]TGTAGGTGACACCAT	51317
rs186278116	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46059175	ATTACGTACAAATAT[C/T]TACGTCCAAGGATGT	51317
rs186280535	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016347	GTAAGGCATTTAAGG[C/T]CCTTAACAACTATAC	51317
rs186297697	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45980319	GCCATCCTACTTCAA[C/T]TCCAATTTCAGTTTT	51317
rs186301913	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46001695	CTGTGTGCATCAGAG[C/T]TAACTGGTATGATAG	51317
rs186301931	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943934	TCAGACAATCCAAAC[A/G]GAGAGGCATTCTACA	51317
rs186309528	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970486	ATCAAAATTTAGATA[C/T]ATTTCTCCCAAGCTT	51317
rs186365705	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45998411	TACTGAGTATATAGT[A/G]TTGTAACAGATGTAG	51317
rs186392699	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062641	TTCCCTTAAATATCT[A/G]GTGATTCTTGGCTAT	51317
rs186399143	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46043356	CATCTGAAGACACAG[A/G]TTACTTCTGTTTACC	51317
rs186400568	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46088408	CCTCTAACTTTCCAA[C/T]AACAACAACAACAAC	51317
rs186402939	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019971	TTTTAAGGGCATTTT[A/G]CTATTTTCTACATTT	51317
rs186418177	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46115787	TCTCTGTTTGAATAG[C/T]AATTAAATACAAAAG	51317
rs186430206	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040105	GTATGAACTGTGCCA[C/G]ATATAACAGGGTTAC	51317
rs186438440	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068868	TGATGCATCTGGTAC[A/G]AGTAACCAACTGACT	51317
rs186465229	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45953946	CCTTTCTGATTTCCA[C/T]GTATTTTAGAATGTG	51317
rs186502901	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45948392	CTTAGTTGGAGATGC[C/T]CTCTTCTCAAAGATT	51317
rs186508598	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45975131	CCAGCCTTGGCAACA[C/T]AGTGAAACTCCACCT	51317
rs186516426	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46017214	GACCTCAGGTGATCC[A/G]CTCGCCTCAGCCTCC	51317
rs186587272	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45950013	GTTTTCCCAGGACAG[C/T]AGTGTGGATAATGAT	51317
rs186594415	snp	A/C/G			intron-variant	PHF21A	GRCh38.p7	11:46087762	TGAATATTTTGAAAA[A/C/G]ATTTTTTTCCTGAGA	51317
rs186603738	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45976424	CAGTGCTTGCACACA[C/G]TAGGAACTCCACAAA	51317
rs186604386	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46043619	ACACGTTACAAAGTG[C/T]CAAAAGGGCCATTAA	51317
rs186609558	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071496	ATTAAAGTGTAAGTT[A/T]CTTCATCAAGCTTAT	51317
rs186610024	snp	G/T	0.0275645	0.114116	intron-variant	PHF21A	GRCh38.p7	11:45999032	GGGTTTCACCATGTT[G/T]GCCAGGCTGGTCTCA	51317
rs186616503	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46051540	TGCCTAAGGAAACCT[C/T]AAACAGAGTACTCTA	51317
rs186642463	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46019083	GGAAGCCTAATCTAA[A/T]TTTTTTTTTTTTTTA	51317
rs186655878	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931618	TGTTGCATTTGCTTT[C/T]AGATCTGTCTTTGTC	51317
rs186668179	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46003009	AAAGATTGAATACTA[C/T]GATTTCTAACTGTTT	51317
rs186747900	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45940649	ACTATGATTTTCTTC[C/T]TTCATTATTAAAATC	51317
rs186790516	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46094884	CAGCCTGGCGACAGA[A/G]TGAGTCTCCGTCCCA	51317
rs186790824	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118851	AAGGAGGGGGCCAGT[C/G]TTCAAAGACCAAAAG	51317
rs186836158	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46063393	AAAAATAACCAGATA[G/T]TAACTACTGTAAGGC	51317
rs186843186	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45957777	AAAAAAAAGAAAAAA[A/G]AAAATAAAGTCTAGG	51317
rs186848536	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46022451	CAAAGTGAGACCCTG[C/T]CTCTTAAAAAAAAAG	51317
rs186872741	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45981808	GAATCCAAATCTGTG[C/G]ATTACTCATTTAACA	51317
rs186921458	snp	C/T	0.00953873	0.0683987	intron-variant	PHF21A	GRCh38.p7	11:46117390	GTAGCTATATTCATC[C/T]TTATGCAGTTACTGT	51317
rs186931965	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46066908	ACAAACACAGTTTTT[C/T]AGTATTTTGCATTTT	51317
rs186933905	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45987799	GTAACTGTCTGTTTA[C/T]AGAACACCGCTGCAC	51317
rs186934414	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045952	CTGTTTTCTTGCTTA[C/T]AGAGATAAAGTACCG	51317
rs186935972	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46100302	ATGAGCATGGACTTT[C/T]TTCCTAAGTCTCTTC	51317
rs186940287	snp	A/C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075409	ATTCATTGGCGTCTT[A/C/G]TCAAACTAACCCTGA	51317
rs186943158	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967487	CACATCCATTGTGGG[C/G]ACCTTGAAGCCATGC	51317
rs186944384	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46024355	TCCTTTCTCCCATGA[A/G]AGTGCTTTCTGCTTG	51317
rs186946292	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45948671	CTGAGTCAGCTTTGC[C/T]AGAATCCTAGTAAAG	51317
rs187038291	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45939842	AATGCCTAGCTCATT[A/C]TCTGGATGGGATTAA	51317
rs187046469	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45965828	GCTTTTGATTCTAAA[A/C]CCTGAGCTCCCTCTT	51317
rs187055129	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45989222	AAACCTGAACTCATC[C/T]TTCAGAATTTCAGAA	51317
rs187061566	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46108422	TGTATAAATCTTACC[A/C]ACCTCTCTTCCTCCA	51317
rs187062762	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009599	CAATCCTAGGAGATA[C/T]GTACTATATAGTATG	51317
rs187076916	snp	C/G	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:46028784	TCACCATGTTGGTCA[C/G]GCTAGTTTCGAACTC	51317
rs187108741	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098889	CTGCATCTGTGAGAA[A/C]CCTTTCTATTGCACT	51317
rs187120234	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46053899	GCATGTGATGATTAC[A/C]ACCCCTCCAATGAGA	51317
rs187120921	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959662	TCCATAAAACAAATA[C/T]TAGAGCTAATAAACA	51317
rs187134879	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46012298	CCTCTCTGCTTTCCT[G/T]TCACCATCTGCTTAA	51317
rs187202414	snp	C/T	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:45952661	GAAAGAATTACATTT[C/T]GTACTTGTTTTAGGA	51317
rs187207830	snp	G/T			missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979903	GCAATGGCTGTATTT[G/T]GAACTTGTCCGGTTG	51317
rs187234710	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992634	TTCTGACTAATCAAA[A/C]TTTTATCATAATGGA	51317
rs187254555	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070949	TTATCAATATATGCT[A/G]TTAATGTGATATAGC	51317
rs187256135	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050968	AAAAATTTACCTAAA[A/G]ATAAATATAGCAGTC	51317
rs187267508	snp	G/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931277	AAAAGGTAAGTTAGG[G/T]GTTGTGTGGCAACCC	51317
rs187284849	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46073855	AGGTCAAGAAGCTGA[A/C]TTTGAAATCTGCCAG	51317
rs187295516	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031229	TCCCTTCCAACCTCT[C/T]TCCATACCTTTTGTC	51317
rs187392711	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032108	AAAGGAGACACACCA[A/G]AGTTTGATTTAGATA	51317
rs187395983	snp	A/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45999294	CTAACTCAAGGAAAC[A/T]TTTTTGAGATTAAAA	51317
rs187401648	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46013067	TTTCCTATATATTCA[C/G]ACCTATGATAAAGTT	51317
rs187442861	snp	A/G	0.0138799	0.0821421	intron-variant	PHF21A	GRCh38.p7	11:45946404	TTATTTATTTTTTGA[A/G]ACGGAATCTCGCTCT	51317
rs187448260	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46084006	TTAAAAGCAGTATCT[A/G]TGACTTTGTCGAGTA	51317
rs187451650	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45970937	CAGGACGCTTCTGTA[A/G]TGATTTGAGCAGATA	51317
rs187459294	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933889	CACTTTCCAGAAATC[C/T]GGCTTTGCTTTTCTA	51317
rs187459672	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45993854	GGGCAGCTGGCGAGA[C/T]AGCTCTGGAGCCTGT	51317
rs187461223	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46040547	TAAAAGACTGGATTA[C/G]TCATTACTGCAGTAC	51317
rs187486859	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46106792	CCATCTCAATGGGAG[C/T]AGAAGCTATCAGGGC	51317
rs187488979	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084451	TCCCTCAAAACAATT[A/C]TTCAAGTATTCCTCT	51317
rs187504584	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975392	TAAAACAAAACAAAA[C/T]AAAATAAAACAGATG	51317
rs187506938	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46061317	GATCCCATATGAATC[C/T]TAAAATAGTTTTCTC	51317
rs187511760	snp	C/T	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46041778	ATATACCCTTCCACG[C/T]TCCCTGAACTATCAC	51317
rs187517682	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45990712	GCAGTCCCTTGATTT[G/T]TTTTTTTTTTTTAAA	51317
rs187518039	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46018593	AAATGCCTTTTAAAT[A/C]CCACTAACCTATTTG	51317
rs187530795	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46054048	ACGTCGTGGCAGTGG[A/G]GGAAGAAAGTTGAAC	51317
rs187555722	snp	C/G	0.00914312	0.0669923	intron-variant	PHF21A	GRCh38.p7	11:45966584	TGAGGTAACATACCT[C/G]ATTTTTAATAGCCAG	51317
rs187569325	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010249	ATGATTAAGTCACCT[A/G]AGACCAGGAACAGTC	51317
rs187602755	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45994118	GACAATTTTAAGATT[A/C]TGTTGCTAACCTTAC	51317
rs187619487	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45946730	GGTTTCTCTGCAATC[A/G]GCATTCTCACAATAC	51317
rs187622514	snp	G/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46004381	GTAAAAAACTTGTAC[G/T]TTTGACCAAAGGAAA	51317
rs187626192	snp	G/T	0.0103295	0.0711199	intron-variant	PHF21A	GRCh38.p7	11:45972257	GAAGCTGTACTTTTC[G/T]AGACTTTTTACTAGA	51317
rs187639844	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45994678	GTCAGGGGTTTTGCT[G/T]TTGCATCATTCTGCA	51317
rs187649893	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46014124	CCCACATGGTGAACA[C/T]AGTACCCAACAGGAA	51317
rs187658272	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46044324	AAAAGAAAATTCATG[C/T]AAGGTAAAAGAAGTA	51317
rs187666557	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45939111	TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC	51317
rs187674519	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45964644	TTTTCAAATAGGATA[A/C]GGTGACTGCCTATAA	51317
rs187683744	snp	C/T	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:46023730	GGAGACAGAGGTGGG[C/T]GGATCGCCTGAGGTC	51317
rs187693243	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46113600	TTTAGGAGGCTGAGG[C/T]GGGTGAATTACGAGA	51317
rs187693442	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105752	AAATTTTACATTTAA[A/T]AAGCACTAGGCCTCT	51317
rs187702489	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029413	TCTTCACTGGCTGGG[C/T]GCAGTGGCTCACGCC	51317
rs187712368	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46060007	CCTCGGCCTCCAAAG[C/T]GCTGGGATTACAGGC	51317
rs187755711	snp	A/C	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46032383	TGCTACCATGTCCTT[A/C]GTTTATTTAATAATA	51317
rs187774322	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45946465	CTCGGCTCACTGCAA[C/T]CTCCGCCTCCCGGGT	51317
rs187787051	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46096300	AATTAAAAAAAAAAA[A/C]CCTCTTGACTCCATA	51317
rs187827155	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990801	TTCCCACATACTCCT[A/G]GCCTCCCCACCCCAC	51317
rs187830597	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111481	ACTCCGTCTCAAATA[A/C]ATAAATAAATAAATA	51317
rs187839056	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45976169	CATTTACTATTTTGA[C/T]GCCATCCTTTTGTTC	51317
rs187844519	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089068	CAAACTGTCCCTAAA[A/C]AGGACAACTCCATGT	51317
rs187850848	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46064676	GAATATATGATTTGG[C/T]CTGTCATTTAACATA	51317
rs187867466	snp	A/C	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45972142	CAATGAAACATGACA[A/C]GGTGAAAACAAACAT	51317
rs187991639	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089853	GGAATCTCTACACAG[A/G]TCATACCTCCACTGC	51317
rs188030105	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46055150	AAGATACTTTGAAGC[A/G]ATCTGAATGTAGAAT	51317
rs188046225	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013437	TAATGGCCCCAAAGC[A/G]AAAGAGTAGTGATGT	51317
rs188057611	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094436	AGAGCTTATGGGCCC[G/T]AGATTCCTTGGCTGA	51317
rs188092989	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042923	TTTCTGTTATTTATA[A/C]ATGATCCAGTCTGAG	51317
rs188099159	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46019700	CAATGAAATTTAGTC[A/G]TATTAGTCTCCGGTT	51317
rs188111239	snp	A/C/T	4.94176e-05	0.00497059	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45949417	CTCTGGCTCAAAGAC[A/C/T]GCTCCACTGTAGACC	51317
rs188112262	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46097627	TTTTACCCTCTCTCT[A/G]ACTATCCAAATCTCA	51317
rs188118280	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073517	CGTAATTTATTGTGG[A/G]GCATTTAGAAAATAT	51317
rs188132362	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45961644	AATTGACGACATGTT[A/T]CATAGAAGTCTTTGT	51317
rs188181739	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089295	ACTATGTATCTAATA[C/T]GTAGGTAGATAAAAT	51317
rs188195248	snp	G/T	0.185487	0.241533	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965336	TTCAAGACTTGGCTT[G/T]CTAAGCTGTACAGTT	51317
rs188206309	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46045173	TGGAGCAAAGTCCCA[A/G]TTGGGTTCCCAAGCT	51317
rs188238313	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929461	GCACAAAACTCCAAA[C/T]ACAAGTCTACCAAGA	51317
rs188254588	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45952544	AATTCTGTGGATGAT[C/T]TCACAAGTTCCTCAG	51317
rs188262658	snp	C/T	0.000395387	0.0140548	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979946	TATCAGGTTCTTCCG[C/T]AGCTGTTCAACTACT	51317
rs188269058	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001293	TGACCACCAGGGGGG[C/T]TGGAAATGGGGCTCT	51317
rs188279512	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46066038	CTGTGAATCTGTAAT[A/T]ATTTCCAAGTAAAAA	51317
rs188297957	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45934406	ACCTAAGGAACAGGG[C/T]GGGTGGAGTGGGTAG	51317
rs188298152	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45958445	ATATATATATATATA[C/T]ATATACACACACACA	51317
rs188310009	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45956988	GAATGGCTATAGTAC[C/T]ATTAGACAAAAGTGA	51317
rs188312612	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985711	GACAAATAGTTTCTT[C/T]CCCTTTTTAACCTCT	51317
rs188319010	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006380	TCAAATCCAGAATTA[A/G]TAAGCACCTAACGAA	51317
rs188331916	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004980	ATAATATTTGTCTCT[C/T]ACTGCAAATGTCTCT	51317
rs188375803	snp	A/T	1.64806e-05	0.00287054	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979869	TGCTGTGCTGTTTGT[A/T]GTTTGTTTTCAGATT	51317
rs188439317	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45950475	TTGGAAGAAGAAGAA[C/T]TGTCTCGAGCCACAC	51317
rs188465813	snp	G/T			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123020	AATACAAATGGGGGG[G/T]TGGGGGGTTTTGTTT	51317
rs188471320	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112430	CACCGTGCTAGGTAC[A/G]GTCATAGATTTTAAC	51317
rs188485312	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46065554	ATAAATTCACTTACT[A/G]TCTTAGCCACTTTTA	51317
rs188499257	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46024095	GAAAGCAAGGAAAGG[A/G]CAAGGTGGTGTCTGG	51317
rs188540353	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070653	TATAATTTTTAAACA[C/G]AGTCAGAGAAGGAAA	51317
rs188548397	snp	A/G	0.0569829	0.158885	intron-variant	PHF21A	GRCh38.p7	11:46079433	GTGACAGTGGCTTCC[A/G]AAAGGAATTTAAGCA	51317
rs188561788	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46027999	TTTCACTACAGCCTA[A/G]TAATACAAACAGGGT	51317
rs188575771	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46095198	ATTGTCAAAAAAAAA[A/G]CAAATATTCTATTTC	51317
rs188576836	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988348	GAAGACAGAAAAAGA[C/T]AATAATATTAGAAAA	51317
rs188585929	snp	A/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46097481	TCATGGCTCACTCCC[A/T]CAAATTATTGAGGAA	51317
rs188589215	snp	A/C	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46073249	GGGAGAATGGCGTGA[A/C]CCCAGGAGGCGGAGC	51317
rs188603529	snp	A/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46053177	GTGTCCTGATAAATG[A/T]TTGGTTTCACAGAAC	51317
rs188607192	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45984590	CAGAAAATCAGGTTC[A/G]TTTTTCCACCGTTTA	51317
rs188607945	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46030470	ATCAGATTTCAATAC[C/T]AGCATTTTAAAAAGA	51317
rs188624326	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933625	GCTCCCCACCCAAGA[A/G]AACAGAAACAAACCC	51317
rs188640768	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984059	AAATGTAGCTAACTA[C/T]ATTGGAACATTATCC	51317
rs188650640	snp	G/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45967809	CTACTGACTTAACAG[G/T]AAGAAATATATTTTA	51317
rs188658918	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991380	GGTAGAACAATGAGG[C/T]TCTGAGTAATTAAGT	51317
rs188666476	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008894	TGACCAGTGTTCACC[A/C]TCCATCTTAATCAGA	51317
rs188668997	snp	A/C	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46010908	AGCATCATACCAGCT[A/C]CTTTCTCTCCTACTA	51317
rs188674065	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977370	TCAAACTCCTGACCT[A/G]AAGTGATCCACCCAC	51317
rs188698988	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932148	AGGGCTGATGCAGCC[A/G]GCCTGTACTCCCGCA	51317
rs188746719	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056562	AGAATGGAGACAGGA[G/T]AAATTAACAGCTTCT	51317
rs188757326	snp	A/T	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:46036882	TTATGTTTAAAAAAA[A/T]TTTTTTTTGTAGAGA	51317
rs188765421	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014480	ATGAACATACAAGTG[C/T]AAGTGTACTTTTTGG	51317
rs188819079	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46093830	AATTTCTTATGCATC[A/G]ATTTCCAGCAGCATT	51317
rs188833660	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049988	GACCATATTCTATCA[C/T]ATATTTCATGTAGTC	51317
rs188840064	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46101207	AGCTAAAATCTGTCC[A/G]GCAGGCATCGTTCTT	51317
rs188858145	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46055785	ATAGCAGGGGATTCA[C/T]TGAAAATATAATACG	51317
rs188909117	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995019	TATATGCAGACCTGG[A/G]AGAAAGACCTAATTG	51317
rs188916155	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45956185	GGGAGTCCCTTCAGG[C/G]TGAAATGAAAGGACA	51317
rs188917045	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960759	CCCTTCGATGAATCT[A/G]AAGTTTGGTCTCTGA	51317
rs188920264	snp	C/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46101682	TTGTTGCCCAGGCTG[C/G]AGTGCAGTGGCATGG	51317
rs188935961	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46077973	CTGGAGTGCAGTGAC[A/C]AGATCTTGGCTCACT	51317
rs188960277	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45941470	GTAAACCCCACTGTT[C/T]GGTCTTGAGAGAATG	51317
rs188974876	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991198	GTTCTTCTATGTTTT[G/T]CATGGTTTGATAGTT	51317
rs189134651	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46076417	GGTAACAAGGTACAC[A/G]CAGCACCTACAAGAT	51317
rs189139810	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46049554	AGGGTGTGGCGGGGG[A/G]AGGAGGGATAGAAAG	51317
rs189146935	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46033676	GCTATCTATCCACTA[C/G]CCATATATGGCTATT	51317
rs189157967	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46086685	GTGTCCAAAATGATT[C/G]CTTATAATTTTTGTC	51317
rs189170898	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087001	ACTAAGATTATATGC[C/T]TTGTCTATCAAACTG	51317
rs189185640	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062717	CTCTCATACACTACT[C/G]AAAGGAATGTAAAAT	51317
rs189189230	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043564	TGAAGTGATAAAGAC[A/G]AGCTCTGCCAAACTG	51317
rs189198480	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45977858	CTTTTTTTTTTTTTG[G/T]TATTGAATGGCAGTA	51317
rs189199941	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46021423	CAAGTATACACCATA[C/T]CTCCATCAGTATTGT	51317
rs189207112	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45947738	GGGGGGCTCCTTTCC[A/G]AGAACTGCATCAGGG	51317
rs189221333	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45996586	GTGCCAGGAATGCTA[C/T]TCTCCATATGCACAA	51317
rs189286168	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46079324	GTGATCCATGTAATA[C/G]GCTCAGGAGACACTT	51317
rs189302861	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46037818	TTTTTTTCCTCCAAA[A/T]TTTCTTGCTTGATGC	51317
rs189334236	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46097017	ACACTCCACATCTAC[C/T]CCGACAGCCAACCAT	51317
rs189357689	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46109111	ATTTCTAGGTATCTA[A/T]GGGAATTACATAGTT	51317
rs189399641	snp	C/T	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:45940448	ATCTGCCCACCTCGG[C/T]CTCCCAAAGTGCTGG	51317
rs189424842	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46108605	ATACATATGTAAATG[A/C]ACAGGAAAAGTTTAA	51317
rs189445269	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46062281	TATATTAGTTATTGG[C/T]TGGTTTTCTCTTCTC	51317
rs189467147	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943031	CATAACCTATATTCA[A/C]TCCTGATGGCTCTTC	51317
rs189495076	snp	A/C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45974027	CCCAACACTTTAAAA[A/C/G]CACTGAAACCTAACA	51317
rs189514193	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46114754	GATTTGTAAGTATGT[C/T]GCTTTGGAGATGCAC	51317
rs189520255	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038288	ATGTGCCACCACACC[C/T]GGCTAATTTTTGTAT	51317
rs189520466	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091819	CAGCTTCCTAAGTAA[A/C]TGGAGCTATAGGCAC	51317
rs189521263	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45955119	TTCCCCCTTTATACT[A/C]AACGCTATGTAAGAG	51317
rs189522149	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068193	TCACATGGAAGTAAC[A/G]CTGCCAAGATTTTCA	51317
rs189526687	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015501	TTATTTCTTCAATAA[C/T]AAATTAACCTTAGCT	51317
rs189530995	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45983004	GCCTAGCTAAAGTAC[A/C]CTAGAAGCAAGAAAC	51317
rs189536036	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46046994	AACAGCTTTACCTCT[A/G]ATAAAGTTTAAGCTA	51317
rs189541671	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46003815	ATTTGCCCTTCATCA[A/G]TTGCTTCCTATGCCA	51317
rs189578708	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057619	ATATGACTCAAGCTG[A/C]AATAAGTAAAATCAC	51317
rs189597803	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46015015	ATAAAAAAATAAAAA[A/T]AAATAAAAAAATAAA	51317
rs189650353	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46061994	GCTTTTCAGAATTTG[C/T]AAAGCATCATTCCAA	51317
rs189671260	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46019035	ATAAGGCAAGAAAAA[C/G]AAAGGGGGAAGAAAA	51317
rs189672508	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46063761	TATATATAATTTTAT[A/C]AGCTATTAGCAGGAA	51317
rs189676511	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044231	TCAAAAGCTGTCCTA[C/T]AGTACAGCTAGAGGT	51317
rs189687053	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023510	TCAGCATTCCTAAAC[G/T]GTGTCATATGGAATA	51317
rs189712482	snp	A/C	0.00557542	0.0525036	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933409	TGATACACTGTCCCA[A/C]CCCCTGCTCCCTCCA	51317
rs189723193	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45966197	TATGTACTGAAGACT[C/T]ACACTTTTACCTCAG	51317
rs189733267	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45951975	CTGCATCCAGCTAAT[A/T]TTTGTATTTTTAGTA	51317
rs189758386	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937953	AAATACAAGGAAGCA[C/T]CTATCCAGCTCAGTA	51317
rs189763825	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45962511	GAGTCTCTGCTGATC[G/T]GGCTCGGTAACCTCT	51317
rs189775644	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987909	TGTCTTGGACACTAC[A/C]GAAATTCTCCCATTC	51317
rs189784228	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46007698	ATTAAATCCGTCATT[C/T]TAAAATTTAGTTACA	51317
rs189815183	snp	C/G/T	0.00954224	0.0684493	intron-variant	PHF21A	GRCh38.p7	11:46068937	TAATGTGGCACGTTA[C/G/T]TAAAGTATAAGTTAC	51317
rs189819122	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048940	TAACATTTTACATTC[C/T]CACCAGCAATGTCTG	51317
rs189830155	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46027173	TCTCACATCACTCTG[A/C]TTTTTCTCCCTGATT	51317
rs189882449	snp	C/T	0.0244538	0.107838	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46121988	CAGCGGCGGCGGCGG[C/T]GGCGGTGATGGGGCC	51317
rs189912463	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085316	TTCAAGCTTGCCAGT[C/T]ATCTCTTTGACTATA	51317
rs189947555	snp	A/G	0.0191293	0.0959101	intron-variant	PHF21A	GRCh38.p7	11:45999860	GTATATAGAAACATC[A/G]TAACTTTTCTCTTGA	51317
rs189976873	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46047826	GCATGTGAAAACTCT[C/G]GGTAAACAATGGCAC	51317
rs189980772	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007598	GGTATTACAGGTGTG[A/G]GCCACCGTGCCCGGC	51317
rs189999807	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092596	CATTAACAAATTAAG[A/G]TAACATCACTAGTTC	51317
rs190034579	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45952679	ACTTGTTTTAGGAAA[C/T]CTGAACTGGCTCAAT	51317
rs190092193	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119607	GCACCCGACAACCGG[C/T]CTGTGGCCTTCTCCG	51317
rs190118495	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46072705	GGAAGGAGTGTCAGG[G/T]ATAGCTCCTCTGAGG	51317
rs190133761	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46030302	TTATTTTTTCTCTCC[A/G]TAAGTTCTCTTGCTC	51317
rs190150494	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45999857	CCAGTATATAGAAAC[A/G]TCGTAACTTTTCTCT	51317
rs190197709	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45946871	TTCAAGTTAACTATT[C/G]TTATCCCTTGCTTTT	51317
rs190203499	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119759	GAAAAAAAAAAAAAA[A/G]AAATCCTAACAGCAC	51317
rs190210216	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46115575	GAGAAAATTAATGTG[A/G]TCAAAACGTTAAAGA	51317
rs190218211	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46068816	ACGTTATTAGGATAA[A/G]CTTACAAGAGGATTG	51317
rs190220677	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931811	GCAAAGGTCTCCAGC[A/G]AGAGCACAAATCTGA	51317
rs190224790	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45954138	AGTACCTGGGATTAC[A/G]GGCACCCGCTACCAC	51317
rs190226643	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987808	TGTTTACAGAACACC[A/G]CTGCACATACCATCA	51317
rs190236993	snp	G/T	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46026850	AAGAATGCTGAGAAG[G/T]CCTTACATCTTTAAA	51317
rs190257488	snp	C/T	0.0123036	0.0774623	intron-variant	PHF21A	GRCh38.p7	11:46074770	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG	51317
rs190261731	snp	C/T	0.00993419	0.0697739	intron-variant	PHF21A	GRCh38.p7	11:46055115	TTCCATTTTGGACTT[C/T]TAAATTATGGCGAGA	51317
rs190269515	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935447	GGTAAGGCACCACCT[A/G]CCAACTGGCCGCCTG	51317
rs190272470	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929939	CAGAGGGACAGGGGC[A/G]AGGTTCACACAGAGC	51317
rs190279949	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46013277	TAAGTTTTAAACTGC[A/C]CGCTTAGAGTAGCCT	51317
rs190284754	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46010684	GGTTTTCTAAGCCAG[C/T]GTGCAAAGCCTTGAC	51317
rs190290833	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45980605	ACAGCCTTGAACTCC[G/T]GGCATCAAGCAATCT	51317
rs190362497	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46096802	AGCACATATCCTTCC[C/T]CTGAATTCCAAACTC	51317
rs190372877	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46052458	GAGTCTTCACTCATA[C/T]ACCTACTGAATACCT	51317
rs190402174	snp	C/T	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:45993967	CTGGGCAGGGCTAGA[C/T]AACTTGCTTCAAAGT	51317
rs190414464	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45936751	AAATATCAGCTTAGG[A/G]GAATCAAGTTCAAGG	51317
rs190415992	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104133	AAATGCCCAAAATCA[G/T]AAAGCAAATAAACTG	51317
rs190435917	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059105	GAAAGTTATGAAGAA[C/G]CATCTATTTATGTAT	51317
rs190436739	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100099	CACAAAGAAACAGGA[A/G]TCTGAAACATGCCTC	51317
rs190458081	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46067651	AATTTTCTTTTGATG[G/T]TGAACCCTTGGTAGG	51317
rs190465076	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025097	AATAAACACACACTG[C/T]CTATCCACAAGGAGC	51317
rs190473933	snp	A/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46009430	ACCTGCCTAGAATGA[A/T]CTGTGAAACCCTATT	51317
rs190487872	snp	A/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45986903	TGGCTATTTTTTTTT[A/T]AATGACAACTGCCAA	51317
rs190534385	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45959058	ATTAAAAGGATGGTA[C/T]ACTATGACAAAGCCA	51317
rs190583044	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46104633	TTGTTCCAAATTTAC[C/T]CTTTTCCCATGAACT	51317
rs190587444	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46082663	CTTTTGAGTCAACAA[A/C]TGTAAATTTAAAATT	51317
rs190591725	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46011775	CAGAGGGGAATTTTA[C/T]GAGTTTTTATTTACT	51317
rs190604752	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46059178	ACGTACAAATATTTA[C/T]GTCCAAGGATGTACA	51317
rs190608809	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46039323	TCTGCTGATTCTCTT[C/T]ATAGAACTGGTAATT	51317
rs190618487	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46015728	TTAGCCTAGGCCTAC[A/G]CAGGGTCACAATCAT	51317
rs190670915	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080936	CCAGAGTAGCTGAGA[C/T]TACAGGCGTAAGCCA	51317
rs190696830	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45944699	CCCCCAGATCCTCCC[A/G]AGGCTTCACCACTCT	51317
rs190697244	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45957819	TGAAATAGAGAAGAA[A/C]AACAGACTCAACAAA	51317
rs190700109	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46109562	AACACAAAAGCTCAT[A/T]ATTAAAATTTTTCAT	51317
rs190702699	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45970527	CAGTTTTCTAAATGG[C/T]TTGATCCTAGAACTC	51317
rs190713131	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992683	TAGTGGGAAAATGCA[G/T]AGACAAAAGGCAAGT	51317
rs190731345	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46088526	TATCTGGAAAGCACA[C/T]TCACCATCCCAAAAA	51317
rs190749414	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46007052	TCGTTTTACAGGTGA[C/T]TTCCCATTACAAAAA	51317
rs190750234	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46012525	AGCTATTTGGTCTTA[C/T]GCAAGTTAACTCACG	51317
rs190756958	snp	A/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46111634	TGCCCTGCTTCTGCA[A/T]ACATTCAAACTAAGA	51317
rs190758045	snp	G/T	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:46053561	TATGTATACCATGAC[G/T]GGTAAAAAGAACCCC	51317
rs190761011	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46089097	GTTCTCTATACCATG[C/T]ATTTATTTGGTGTGA	51317
rs190765137	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46064708	TCAACATTTTAAAAA[A/G]GAGAAATCCAAAACA	51317
rs190772260	snp	C/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45970053	ATTAACACTGCATTA[C/G]GAAACTTTTTAACTC	51317
rs190777553	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044776	CTTCTACAAGATAAA[A/G]CACTGATTCAATTCT	51317
rs190854456	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45949558	CATTGTTTTATCTAT[C/T]GGTTTTCCCATAAGA	51317
rs190866906	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998474	CCACATCTATTTTAG[A/G]AAACAGAAGATGTAC	51317
rs190899684	snp	C/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:46093383	ATCTTTGTTTAACCA[C/T]GTACAGTTATACCAA	51317
rs190901741	snp	A/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46116982	AAAAAATAAAAAAAT[A/T]AAAAAACTATAGTGT	51317
rs190915085	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070528	TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC	51317
rs190963431	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46111245	AGGCCGAGGTGGGCA[G/T]ATCACTTGAGGCCAA	51317
rs191004519	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943312	ATATTTAGTAGAGAC[A/G]GGGTTTCACTATATT	51317
rs191014378	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46031057	TACAGGAAATTCATG[C/T]ACGACAAGCGATCAC	51317
rs191024644	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992256	AAAATTTTTCAGCCC[A/G]GCATGGTGGCTCATG	51317
rs191058111	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46116034	TCAAAAGAATAGTCA[C/T]TTCTAAAATTTAAGA	51317
rs191059969	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46083263	AGTTTAACGAGATCC[A/G]GAGCAGCAGCAGGGA	51317
rs191069313	snp	G/T			missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979874	TGCTGTTTGTAGTTT[G/T]TTTTCAGATTGTGGC	51317
rs191075459	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46040338	TGATGACACTACTGG[C/T]AGTTATAAACAAAGA	51317
rs191107645	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45976197	TTCATACTACTCTCT[A/G]TACTTGTGAAGCTCT	51317
rs191132016	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46016349	AAGGCATTTAAGGCC[A/C]TTAACAACTATACTT	51317
rs191143440	snp	C/T	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:45948596	TGGGGTTCTGTTCAC[C/T]GTGCTATTCATGGAT	51317
rs191155538	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45975218	ACTTGAGAGGCTGAG[A/G]TGGAAGGATCACCTA	51317
rs191163495	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45997978	TCTGAACACTGGGCT[C/T]GTAAGGAGGATGGCA	51317
rs191207094	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110391	TTAAAAAAGAAAACT[A/G]TGTTCAATAATTTAG	51317
rs191220225	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46063470	AAGCAGTCAGTCATA[C/G]AGAATATGTAAATGT	51317
rs191234728	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022553	TGCAGCCTCAAACTC[C/T]TGGGCTCAAGCAATC	51317
rs191277165	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985929	AATTGACAACAGCAG[C/T]AACTGTAATTATCAG	51317
rs191286992	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006733	GTATTAAGTATTGAA[C/T]TGTCTTAAACGCCTA	51317
rs191288602	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46105390	CACAGGACATGCCCC[C/T]GATGATTAGATCACT	51317
rs191306900	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059310	AAATGATAGGATACT[A/G]TCAAGCCACTAAAAA	51317
rs191317704	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45981898	GTTCTCTTGAGAGTT[G/T]TTTGTTTTTATTTTT	51317
rs191325526	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946426	TCTCGCTCTGTCACC[C/G]AGGCTGGAGTGCTGT	51317
rs191331153	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46090043	TATACACATTCTTCT[A/G]TTTCCTAACTTTCTT	51317
rs191345477	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067848	TGCAAATAAGTACCA[C/T]AATGAGCGCCAAATA	51317
rs191351717	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46046061	CAGCTTTGTGAGCTC[C/T]GGCATTCAGCTAGCC	51317
rs191351763	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46100587	GTTAAGTAAGTATAC[C/T]CCTTGCACTAAATGA	51317
rs191358284	snp	A/G	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46024804	GACTCCATCTCAAAA[A/G]AAAGAAAGAAAGAAA	51317
rs191383663	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45975998	AATATATGCCATATA[C/T]AACCTCCCATTTGTC	51317
rs191440553	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46087932	GGCTAATTTTTGTAT[C/T]TTTTTGTAGTGACAG	51317
rs191463810	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46043780	GAGATGAGAGGACCC[C/T]GCTGTCATATACCCA	51317
rs191490205	snp	C/T	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:46017575	TTCAGGATTTGCCCT[C/T]AAGGGGGAAAAAAAA	51317
rs191516429	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46094279	ATAAAGAATTTTGCC[A/C]TGATATCCTGAAATC	51317
rs191526961	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46050056	GCAATTAAAAGAAAA[C/T]TAGCAAGTCTTTCCC	51317
rs191562906	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46003527	ACTTGATTTTTAAAA[C/T]ACCATAAAGCTGCCC	51317
rs191571015	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45971873	GGCTGGGGTAAAAGG[A/T]CAGTGTCTTTTTCTT	51317
rs191635096	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45998369	TAGGCAGTATAAGGT[C/T]TGAAGACAATATTAA	51317
rs191652816	snp	G/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46117908	TTATGAATGGAATTT[G/T]TAAATGGACTTACTC	51317
rs191656309	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094636	GTGGCTCATGCCTGC[A/G]CTCTGGGAGGCCAAA	51317
rs191659643	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071174	CTAATGAGATGTTAA[C/T]AAACCTGATGCCAGC	51317
rs191668664	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46051441	TCCATTCTCATACCA[C/T]CTTGGGCACAAAAGA	51317
rs191675991	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028824	TCGTCCACTCGCCTC[A/G]GCCTCCCAAAGTGCT	51317
rs191678492	snp	A/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119111	AGTGCACAACTGCTT[A/T]AAAAAAAAAAAACTT	51317
rs191695337	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032045	CAAAGCCCAACTCTT[A/C]AGTGCTGCTTTAAAA	51317
rs191696160	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45989306	GAGAGGTTCAGCATT[G/T]TAGAAGAAAAGCATG	51317
rs191699060	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952210	GGCAGTGATTCTGTC[C/T]AACTAGAAGGTGAAC	51317
rs191703474	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46009707	AGCAGACTTCCAACT[C/T]GGGCAGTTTGGCTAC	51317
rs191709976	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45978796	CTTTTTGTGTATCTT[A/G]ATTGCCTCACGATTC	51317
rs191732233	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46108557	AACTTCTTTAAAAAT[A/G]TGTGTGTGTGTATAT	51317
rs191763653	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46087552	ATTTGAAATTCTTTT[C/T]CTTTTCTTCAGAAAG	51317
rs191776721	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070758	GAAAGAACAACAAAA[C/T]TTAAAACCAAAAGAT	51317
rs191798218	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46028189	CCTATCCCAAAAATT[G/T]CAACATTCCAAAGAG	51317
rs191828200	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949100	AAGGGTTTTATTGTA[G/T]GTACTTGGCTCTCAG	51317
rs191845560	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101797	CATGCCACCACACTC[A/G]GCTAATTTTTGTATT	51317
rs191858453	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078325	AACTTGATTTTACTT[G/T]ACAGTGAAGCCTGTA	51317
rs191858932	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46056690	GGCTCTCCCAATCAA[C/T]GAATCAGGATTTAGC	51317
rs191867985	snp	A/G	0.0130921	0.0798413	intron-variant	PHF21A	GRCh38.p7	11:46037435	TCACCTGAGGTCAGG[A/G]GTTCAAGACCAGCCT	51317
rs191872503	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46074082	GAACTAGTGTCTACC[A/G]CAAGAAATAGTGACT	51317
rs191874553	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46014660	CCATAGCCTCTCCAA[C/T]ATCTGTTATTTTTGA	51317
rs191903911	snp	C/T	0.000182377	0.00954754	missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934077	GTGCAGTCCGGGCCA[C/T]TGGAGATGGCCCCCA	51317
rs191918382	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957257	AAAAGGACATAGGGA[A/G]CTTGAACAACACTAT	51317
rs191922923	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45985315	AGAAGAGGGGATGTG[C/T]TACTGTCATAACATT	51317
rs191964525	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45939244	GTAGAGGACAACCTA[C/T]ATATCATAAATCTTA	51317
rs191966573	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45965166	ATGACCCTTCTGCAC[A/G]TGGATGAATTATCGC	51317
rs191993426	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46061708	AACCTAAACTGGCTG[G/T]TTTCTAAACCTGTTG	51317
rs191995893	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46027368	TAACAGGTTTGCACT[C/G]CTGCATTTTTCTGTT	51317
rs191998539	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107008	TACCAACTGTCCTCC[A/T]GCTGTCCCCACGGCT	51317
rs192003721	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085160	TAACAAATTAATACT[C/T]AAAACAGACAAATAC	51317
rs192017753	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46061580	ATTAATTCTTTCCCA[A/T]ACTTTCCAAAGAAAC	51317
rs192022276	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041809	ACATCTTTCTTCTCC[C/T]ATGAACCATCTGAAA	51317
rs192053474	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45940652	ATGATTTTCTTCCTT[C/T]ATTATTAAAATCAGG	51317
rs192067671	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45938573	TGGATGCCTGAAACC[A/T]CCGTACTGAACCCTA	51317
rs192078513	snp	G/T			missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979910	CTGTATTTGGAACTT[G/T]TCCGGTTGTTCTTGC	51317
rs192081124	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988337	AAGTTTTCTTAGAAG[A/T]CAGAAAAAGACAATA	51317
rs192102965	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45983397	ATAGCGTTGGTATGT[A/C]AAACTGCCACTCAGA	51317
rs192119247	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46075523	AATCACATTCAGAGC[A/C]AAATACATACTAACC	51317
rs192160990	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972166	CAAACATCTGAGTTT[C/T]AAAAGCCTGAGAGAT	51317
rs192162344	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099403	GAGGATGAGCAAAAC[C/T]AACTAAATAAAAATT	51317
rs192170222	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934663	GAGCTCTCCAGGGTG[C/G]AAAACACACAGTGCT	51317
rs192185367	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46054034	CTTTTTCACAAGCAA[C/T]GTCGTGGCAGTGGAG	51317
rs192196743	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946733	TTCTCTGCAATCAGC[A/C]TTCTCACAATACTTT	51317
rs192252328	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055336	ATAATAGTTAATTAA[A/C]TTACAGTAACAAGAA	51317
rs192322758	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46049632	TGTCACAGCACTCTC[C/T]TTGCTGGTTGCCAGC	51317
rs192364967	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46034844	AGGGGATAGTGGGCA[C/T]GTGACCCTGGCCACA	51317
rs192371857	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46014253	CCCACTTATAAATGA[C/G]AACATATAATATTCA	51317
rs192404413	snp	C/G	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:45973267	ACATCACAGAAAGTT[C/G]TATCACTGTGCAATA	51317
rs192412201	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45994822	ATATTCACTGGCAAC[A/G]TGACACACTAGTAAC	51317
rs192415184	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45966325	ATCTTCTCTTCCTCC[A/G]ATAATTGCCTCAGTA	51317
rs192436479	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45963986	GGCAGGTCACTTGAG[A/G]TTGGGAGTTTGAGAT	51317
rs192458973	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46008418	AAAATTCCTCTCTTG[C/G]TTTCCTGAAGGACTC	51317
rs192493544	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46060199	GATGGGGTCTTGCTA[A/C]GTTGGCCTGGCTGGT	51317
rs192512137	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041052	AGGTCGCCCTCACTG[A/T]CTTTTCATGGTGAAT	51317
rs192521219	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46017719	CAAATGCAAATGATT[C/T]TGTCCCTAAAAACTG	51317
rs192539534	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946491	CGGGTTCAAGCCATT[C/G]TCCTGCCTCAGCCTC	51317
rs192553069	snp	C/T	0.0876345	0.190099	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086229	GTTCATGCCATTCTC[C/T]TGCCTCAGCCTCCTG	51317
rs192557847	snp	A/C	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45994551	GTGACGCAGCCATCA[A/C]TTCTGCTTAGTCTCC	51317
rs192575247	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042417	TCATCACCACTTGAG[A/C]TGGTCTACGCTGAGG	51317
rs192648579	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46000253	ATTATTCACTTCTAC[A/G]CTATATGCCAAGGAA	51317
rs192655307	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45950362	AGCCCAATGGGCGGG[A/T]CTCATGAATGCACAA	51317
rs192655802	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075657	AAGACAAGATGGGGA[C/T]GCATAAGAATAGGAG	51317
rs192662841	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45976439	GTAGGAACTCCACAA[A/G]TATTTACAGAATGAA	51317
rs192668534	snp	A/G	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119343	TGATGAGGCCCACAC[A/G]TGCCCGGACCTTCAC	51317
rs192669300	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45999170	AACAAAGAAAATTAT[C/T]AGAAAATTTAAAAAC	51317
rs192669930	snp	C/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46094961	AATGGGCTTCAGAGG[C/G]GTCTGTCAACTGCTT	51317
rs192673551	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46033116	TTGTATTTTTTCCCA[A/G]GTCTCATGAAATTCT	51317
rs192700184	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46046403	ATGGCAAAAGAGAAA[A/C]CAAAAACTAAAACAA	51317
rs192712036	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024105	AAAGGGCAAGGTGGT[A/G]TCTGGGGATATCTCC	51317
rs192718094	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46079429	ACGGGTGACAGTGGC[C/T]TCCGAAAGGAATTTA	51317
rs192750358	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45962307	GGATACGGGTTTGGT[A/C]ACTGTGAACAGGTGT	51317
rs192757314	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45939899	GGAAGACTGAAGGGA[A/G]GTGCTAGAGGTGACC	51317
rs192760271	snp	C/T	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:46114277	GCTAGAATTTACATA[C/T]ATACAGTTGCTACAC	51317
rs192795272	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112814	GGCTTCTCATGCCCA[C/T]ACTAGCAATGAATGA	51317
rs192799478	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46065776	TGAAGCACTAGGGTA[C/T]AAAGCGGGTGTATAA	51317
rs192822861	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978396	GGAGTATGTCCATTA[C/T]GTAAAACACTTAGGA	51317
rs192828694	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46108463	CACTTCCCACATGAG[A/C]CCTATTTTCAAAAAT	51317
rs192835366	snp	A/C			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119629	CCTTCTCCGGGGGTG[A/C]AAGCCACAGACAAAG	51317
rs192838812	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46062072	ATTCCCAATCCCTGT[C/T]TGCAACTGTTTTTTG	51317
rs192845304	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019185	TTTCGCTTTATCTTC[C/T]CTAAAGAGGAAAAGA	51317
rs192855245	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46022145	ATGTACTGTTTGTTT[C/G]TTTCTTTTTTTATTT	51317
rs192874774	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018832	TCACTTAATGGCACT[A/G]CTTACTGCATACCAT	51317
rs192913067	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045354	GAGGCTGAAAATATA[C/T]TTCCTGGCTGATTAA	51317
rs192946120	snp	C/G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45956610	TGGGGTTAATTCAAA[C/G/T]TAGATTGTTAAAAAC	51317
rs192947111	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46097020	CTCCACATCTACTCC[A/G]ACAGCCAACCATGTG	51317
rs192968851	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46006509	AAATAACAAGGAGTC[A/T]AAAAGTTTACTGCCA	51317
rs193002042	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005087	CATCAGTAATTTCAC[C/T]TTCTGCAGGCTCAGT	51317
rs193003139	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46089615	GGTAAGGCTGCTATG[C/T]TAAAATTCTGGTGTG	51317
rs193009513	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933035	ACACACACCTGGGTC[A/G]CGTGCTGCTTCACTC	51317
rs193024895	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46077602	CCTGCTTGGTCTTCT[C/G]TCAGGGTTAGGGAAC	51317
rs193025277	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45951651	CTAACTGTTGTTCTT[C/T]TGATGAAGCAGTGTG	51317
rs193034258	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45999588	TTAAAAATATATCTA[C/T]AGAGGACAAAAAATG	51317
rs193052497	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46004554	TTTATCAGTAGCTAT[A/G]ACAGAATATTCTCTA	51317
rs193141452	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45941144	GGCTCTGTCACCCAG[A/G]CTGGAGTGCAGTGCT	51317
rs193146008	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071552	TTGACCAGTTAGGTA[A/T]AAGTACTGGCAGTGT	51317
rs193147755	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45990863	AGAACATTTGTTACA[A/G]TCGAACCTACACTGA	51317
rs193150987	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46106158	GGCATCTGTTCCAAG[C/T]ACAGCATGCTAACAT	51317
rs193161257	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029507	AGCCTGGGCAACATG[A/G]TGAAACCCTGTCTCT	51317
rs193172065	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933776	GGTCCAATCTTTGCA[C/T]GTACACACAGAATAA	51317
rs193174046	snp	A/C/G	0.00636936	0.0560724	intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119840	ACTGCGTGCACGACG[A/C/G]GGCTGGACCAAACGG	51317
rs193177827	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984200	TGGAAAGAACAAAGA[C/T]GGAAGGGAGAGAGGG	51317
rs193190178	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45947338	AGGGCCAGAGAGATA[A/C]AAAACTGCCTATAAG	51317
rs193214259	snp	A/C	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46101220	CCAGCAGGCATCGTT[A/C]TTCACTAAGTTAGTG	51317
rs193218489	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056244	TTTTCATTAAGTCTT[C/T]CTCAAGAGAGTCAAT	51317
rs193226314	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46023766	TTTGAGACCAGCCTC[A/G]CCAACATGGTGAAAC	51317
rs193297446	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966682	TGGAGTGCAGTGGCG[C/T]GACCTCGGCTCACAG	51317
rs193299849	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46051682	CTTGAAGGAAGAGAA[C/T]GGTCATCATGCCTCA	51317
rs193301047	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010535	ATTGTTTGGGAATAG[C/T]GGTATGAATAACTCA	51317
rs193302389	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46084053	GACATGACTCTTGGA[C/G]AAAATTGTCTTAAAG	51317
rs199528573	in-del	-/ATG			intron-variant	PHF21A	GRCh38.p7	11:45961639	CTCTGAATTGACGAC[-/ATG]TTACATAGAAGTCTT	51317
rs199531698	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46026644	AAATGCAAAAAAAAA[-/A]TCCTTTAAAGTCAAG	51317
rs199541583	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46015028	AAAAAATAAAAAAAT[A/T]AAAAATAGTTATTCT	51317
rs199576324	snp	A/G	0.00135589	0.026002	intron-variant	PHF21A	GRCh38.p7	11:46076720	TCTTTAGAACACAAC[A/G]TTAAAAATATGCCCC	51317
rs199611691	in-del	-/G	0.0185938	0.0946107	intron-variant	PHF21A	GRCh38.p7	11:46023573	CTGAAAAAGAGGTTA[-/G]GTAAGTTTACCAAAT	51317
rs199654625	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46044303	CCTTAAATGAGCAGG[-/A]AAAAAAAAAGAAAAT	51317
rs199703750	snp	A/G	0	0	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935716	AACTCCATTTAAGTA[A/G]CTTCTGTTTCTCTTC	51317
rs199731971	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46108586	ATATATATATATATA[A/T]AAAATACATATGTAA	51317
rs199772789	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45987250	GACTGTATCATAAAT[A/G]AATGTATGTATGTAT	51317
rs199773972	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46078478	ATAAATATAATTATC[A/C]GAAGACAAGGTAAGT	51317
rs199788684	snp	C/T	0.000115307	0.00759211	intron-variant	PHF21A	GRCh38.p7	11:45948883	ATACAAAAAGGTCCT[C/T]ACCTCTCTTCCGGGT	51317
rs199802844	snp	C/T	0.000149513	0.00864489	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934070	AGGGGGGGTGCAGTC[C/T]GGGCCATTGGAGATG	51317
rs199825140	in-del	-/GTGTGTGTGT			intron-variant	PHF21A	GRCh38.p7	11:46030831	TGTGCGTGTGTGTGC[-/GTGTGTGTGT]GTGTGTGTGTGTGTG	51317
rs199856574	snp	A/G/T			intron-variant	PHF21A	GRCh38.p7	11:45982450	TGCAGAATAATAAAA[A/G/T]TGCAAATTAATAAAA	51317
rs199860171	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46095188	CCATTTGGAAATTGT[A/C]AAAAAAAAAGCAAAT	51317
rs199880109	in-del	-/AAAATAAAATAAAATAAAAT			intron-variant	PHF21A	GRCh38.p7	11:45975323	TGTCTCAAAGAAAAC[-/AAAATAAAATAAAATAAAAT]AAAATAAAATAAAAT	51317
rs199945884	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45983644	GAGGCCCTGCAGGCT[C/T]TTCCAAGGACTGGGA	51317
rs199951563	snp	A/G	0.000132345	0.00813358	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945941	AGTCAGGATGACTGG[A/G]TTGGGGGGATGTTGG	51317
rs199964791	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975342	TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT	51317
rs200011860	in-del	-/ATAT	0.00993419	0.0697739	intron-variant	PHF21A	GRCh38.p7	11:46068723	TAGCCCAGTGTCAAC[-/ATAT]ATAACACCTGATGAC	51317
rs200048370	in-del	-/CCT			intron-variant	PHF21A	GRCh38.p7	11:45989837	ACCCTGTCTCTACAA[-/CCT]AAAATACAAAAATTA	51317
rs200063673	snp	C/G	0.00065136	0.0180348	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933924	CTTCAGTGTTCTGTT[C/G]TCCTTGCCGCCGGGA	51317
rs200068069	in-del	-/CAGC			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932143	CACCAAGGGCTGATG[-/CAGC]CAGCCTGTACTCCCG	51317
rs200100464	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45990725	TTGTTTTTTTTTTTT[A/T]AAGAAGACTTTATTT	51317
rs200108521	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45976635	CACTTGAGCTCCGGA[-/C]GTTTGAGACCAGCCT	51317
rs200112268	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46110569	ATATTTTCTATATTG[C/G]CCATTAACACCAGGG	51317
rs200169232	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45981940	TCTCTTTTTGTTTTT[C/T]TTTTTTTTTTTTTTT	51317
rs200194466	snp	A/G	0.000444719	0.0149051	intron-variant	PHF21A	GRCh38.p7	11:45948859	AAAAGCAACAGCAGC[A/G]AGGGAGAGATACAAA	51317
rs200196294	in-del	-/T	0.0379877	0.132479	intron-variant	PHF21A	GRCh38.p7	11:46062450	TTTTGTTTTCCAACC[-/T]TTTTTTTTAAATCAA	51317
rs200198960	in-del	-/AAAAC			intron-variant	PHF21A	GRCh38.p7	11:45975372	AAAATAAAATAAAAT[-/AAAAC]AAAATAAAACAAAAC	51317
rs200215482	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45986110	ACACACACACACACA[C/G]AGGTATTTACATCAA	51317
rs200231857	in-del	-/AAC	0.0347861	0.127212	intron-variant	PHF21A	GRCh38.p7	11:46088409	CTCTAACTTTCCAAT[-/AAC]AACAACAACAACAAC	51317
rs200274699	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45958443	ATATATATATATATA[C/T]ATATATACACACACA	51317
rs200282795	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45957752	AACTAAATTCAAAGC[-/AA]AAAAAAAAAAAAAAA	51317
rs200291138	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45944096	CTGAAGCAGGAAAAA[A/C]AAAGTGTCACAAAAG	51317
rs200299045	snp	A/C	0.00199806	0.0315443	intron-variant	PHF21A	GRCh38.p7	11:45935621	TCGACTGCTGAAGGC[A/C]TGAGGTTTACTTACA	51317
rs200340010	in-del	-/T	0.0524604	0.153226	intron-variant	PHF21A	GRCh38.p7	11:45982389	CTCTCTGAGTAAATA[-/T]TTTTTTTTAAATGAT	51317
rs200356197	in-del	-/T	0.204189	0.245767	intron-variant	PHF21A	GRCh38.p7	11:46032479	CAAATACACCAAATG[-/T]TTTTTTTCAATTCTC	51317
rs200409253	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45968227	AATTTATTCTCTGCA[C/T]AGAGGCAAGAAGGAA	51317
rs200410948	snp	C/T	3.29647e-05	0.00405971	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935641	GTTTACTTACACTTA[C/T]GGAATTGCTGAGCTG	51317
rs200420666	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46114150	AAAGAACACTTAGAA[A/G]AACAGTATTCCAACT	51317
rs200425880	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46015031	AAATAAAAAAATAAA[A/T]AATAGTTATTCTGAC	51317
rs200459741	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46113825	GTGAGATTCATTCTC[A/C]AAAAAAAAAAAAAAA	51317
rs200504325	in-del	-/AC	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:45991557	CTGCAGTAAGCTTAT[-/AC]ACACACACACACACA	51317
rs200548180	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46019081	CTGGAAGCCTAATCT[A/T]ATTTTTTTTTTTTTT	51317
rs200586865	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46099992	ACTGCTATCCTTAAT[C/G]AACATTTATCTTTTT	51317
rs200599552	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45987251	ACTGTATCATAAATA[A/T]ATGTATGTATGTATG	51317
rs200621220	in-del	-/C			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120335	GAGGAGCCCCAGCTA[-/C]CCTCCCCGGCCGAGG	51317
rs200626824	in-del	-/C	0.0573587	0.15934	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929391	TCAGCTGCTCTGTAT[-/C]CCCCCCCCACCCCCT	51317
rs200675961	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45977895	AGTAGTTGAATGGAC[A/C]TATTTTTCAGCCAGA	51317
rs200709354	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45970582	TTCCTCCTTAAAGGG[A/T]TTTTTTTTTTTTCCT	51317
rs200756167	in-del	-/TA	0.0310518	0.120672	intron-variant	PHF21A	GRCh38.p7	11:45948096	TTTCTAGCCTGCAAC[-/TA]TATAATTCAGGGACA	51317
rs200779604	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45940198	GATTTTAATCTTTTT[C/T]TTTTTTTTTTTTTTA	51317
rs200842546	snp	A/G	6.5912e-05	0.00574035	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971183	GTGACCTTACTAGAC[A/G]TCTGGAGGTTGACTG	51317
rs200885533	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45964179	CTCCAGCCTGGGCAA[C/T]AAGAGTGAAACTCCA	51317
rs200890179	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46118436	AAAAAAAAAAAAAAA[C/G]CCCCTGGAATATTCG	51317
rs200912466	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46069512	GTATTAGAGGCTGGA[A/G]ATAGTCATATATCAG	51317
rs200941157	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45998611	CCACCTCCCAGGTTC[-/G]AAGTGATTCTCCTGC	51317
rs201036024	snp	G/T			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122539	GTTCTTTTGTTCTAA[G/T]GGGGATGATGGCATT	51317
rs201084175	snp	C/T	0.000624334	0.0176572	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965558	TGCGAGCATGGGAGG[C/T]GGTGCTGGGGCAATA	51317
rs201119569	in-del	-/A	0.0178098	0.0926698	intron-variant	PHF21A	GRCh38.p7	11:45974023	TTAACCCAACACTTT[-/A]AAAACACTGAAACCT	51317
rs201121653	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46015027	AAAAAAATAAAAAAA[-/T]AAAAAATAGTTATTC	51317
rs201149103	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46083169	AACAGAAGCAAAGTT[A/T]AAAAAAAAAAAAAGT	51317
rs201159425	snp	C/T	7.00611e-05	0.00591825	intron-variant	PHF21A	GRCh38.p7	11:45938107	ATTCCTCCTGATGGC[C/T]GTGTCTTTGTCCTCC	51317
rs201187984	in-del	-/TTTTTTTTTTTTT			intron-variant	PHF21A	GRCh38.p7	11:45990251	AGCATTTTCATCTTC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTCA	51317
rs201221455	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45962534	TAACCTCTAAGACTA[A/G]TATGCCAGGCTGCCC	51317
rs201229795	snp	C/G	0.000264162	0.0114896	intron-variant	PHF21A	GRCh38.p7	11:46079180	TTCTGGTAATAAAGA[C/G]AGAAAAAGAGCCATC	51317
rs201236542	snp	G/T			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123028	TGGGGGGGTGGGGGG[G/T]TTTGTTTTTAAAGCT	51317
rs201250058	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46101013	ACAAGAAGGAAGTGC[-/G]GAACAAGACTTGTGA	51317
rs201256842	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45951825	TTTTTTTTTTTTTTT[G/T]AGGCGGAGTCTCACT	51317
rs201263397	snp	A/G	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945958	TGGGGGGATGTTGGG[A/G]TAAGGGCTCCAAACC	51317
rs201273053	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46007321	TTTCTTCTTCTTCTT[-/C]TTTTTTTTTTTCGAG	51317
rs201274088	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45957439	ACATAAAATCTCTTC[A/C]CCAGCCACAATGGAA	51317
rs201277471	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45966196	CTATGTACTGAAGAC[C/T]CACACTTTTACCTCA	51317
rs201296262	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45986697	AATTAATGGTGGGGA[A/T]TGCTTAGGAAACTGT	51317
rs201322815	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46092095	GAGAGCCTATTTGCC[A/C]AAAAAAAAAAAAAAT	51317
rs201386236	in-del	-/C	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46116319	GATATACATCTTTTT[-/C]CACTGTGAAACAAGC	51317
rs201402902	snp	C/G/T	0.0001154	0.0075953	intron-variant	PHF21A	GRCh38.p7	11:45936487	GTGGGTATGGATAAC[C/G/T]CCTTACCTGCTTTGT	51317
rs201494316	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45962232	GAATGATGTTATCAT[-/C]TAAAGGGAATAGCAG	51317
rs201509628	in-del	-/T	0.386417	0.209501	intron-variant	PHF21A	GRCh38.p7	11:46110789	TCTACATATTAACAA[-/T]TTTTTTTTTTTTTTG	51317
rs201548405	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46035505	CCTTGAATAGGCAGG[G/T]GGAGTCCTGACTCTC	51317
rs201551932	in-del	-/ACACACACACACACAC	0.0265607	0.112138	intron-variant	PHF21A	GRCh38.p7	11:45955284	GTCTTTCTCTCTCCA[-/ACACACACACACACAC]ACACACACACTTTTT	51317
rs201560749	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46030830	GTGTGCGTGTGTGTG[C/T]GTGTGTGTGTGTGTG	51317
rs201561875	in-del	-/ATCTATCT	0.28853	0.247013	intron-variant	PHF21A	GRCh38.p7	11:46015896	TGCTGTTTTACAGTC[-/ATCTATCT]ATCTATCTATCTATC	51317
rs201568164	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46019083	GGAAGCCTAATCTAA[-/T]TTTTTTTTTTTTTTA	51317
rs201583561	in-del	-/TA	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46034287	TTCATAAGAACTCTT[-/TA]TATGTAAGACTAATA	51317
rs201588912	in-del	-/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120342	CCCAGCTACCTCCCC[-/G]GGCCGAGGGACAGCC	51317
rs201598869	snp	C/G	0.00199799	0.0315437	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965474	GGGGTGGATGGAATT[C/G]TGGGATGTGGGAAGG	51317
rs201604131	in-del	-/CT			intron-variant	PHF21A	GRCh38.p7	11:45966194	TCTATGTACTGAAGA[-/CT]CTCACACTTTTACCT	51317
rs201623034	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45999057	GTCTCAAACTCCTGA[C/G]CTCAAGTGATCTGCC	51317
rs201635943	snp	A/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119557	TACCCTCATCACAAC[A/T]ACTCAACTACTTAGA	51317
rs201644980	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45976633	GATCACTTGAGCTCC[-/G]GAGTTTGAGACCAGC	51317
rs201659362	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45940662	TCCTTCATTATTAAA[A/T]TCAGGCTGAGGGCTA	51317
rs201681285	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46037642	TGAAACGTCATCTCA[A/G]AAAAAAAAAAAAAAA	51317
rs201686192	snp	A/C	1.65042e-05	0.0028726	intron-variant	PHF21A	GRCh38.p7	11:45936469	GGGGAAGCTTACAAA[A/C]AAGTGGGTATGGATA	51317
rs201689293	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45983494	CTGTTGCTATCTGTG[-/A]AAAAAAAAAAATTTT	51317
rs201717253	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46003285	AAAGGCTAACATTCA[A/C]AAAAAAAAAAAAATG	51317
rs201744847	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45964200	TGAAACTCCATCTCA[A/T]AATAATAATAATAAT	51317
rs201791025	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46069513	TATTAGAGGCTGGAG[A/T]TAGTCATATATCAGG	51317
rs201837972	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45953751	TGTGGAACATATTAA[C/T]AAAAAGGTTAGTATT	51317
rs201847139	in-del	-/GTGTGTGTGTGT			intron-variant	PHF21A	GRCh38.p7	11:46030831	TGTGCGTGTGTGTGC[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG	51317
rs201895719	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:46003284	TAAAGGCTAACATTC[-/AA]AAAAAAAAAAAAATG	51317
rs201896668	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45981934	TGTTTCTCTCTTTTT[G/T]TTTTTCTTTTTTTTT	51317
rs201920627	snp	A/G	1.67646e-05	0.00289517	intron-variant	PHF21A	GRCh38.p7	11:46079118	ACAATTAAATGAATA[A/G]CAATAGTAGTTTTAC	51317
rs201935651	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46094717	GAATAATAATTATTT[C/T]GTAGAAGTCTCTACT	51317
rs201941105	in-del	-/AGCCA			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932144	ACCAAGGGCTGATGC[-/AGCCA]GCCTGTACTCCCGCA	51317
rs201951727	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46110803	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC	51317
rs201978704	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45962686	GCCTGAGGTCAGGAG[-/A]TCTGAGACCAGCCTG	51317
rs201995682	snp	A/C	0.00299544	0.0385843	intron-variant	PHF21A	GRCh38.p7	11:46084113	ATGGACTTGTTTACT[A/C]ATCTTAGCCATTACT	51317
rs202003023	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45998614	ACCTCCCAGGTTCAA[-/G]TGATTCTCCTGCCTC	51317
rs202030833	snp	C/T	0.00384513	0.0436782	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933943	TTGCCGCCGGGATCC[C/T]GTGGCTTCTCCTAGA	51317
rs202068536	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45940655	ATTTTCTTCCTTCAT[G/T]ATTAAAATCAGGCTG	51317
rs202073249	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46105615	CTTCCCAAACACCAT[-/A]AAAAAAAAACACAAA	51317
rs202099254	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46026843	CATCACGAAGAATGC[C/T]GAGAAGGCCTTACAT	51317
rs202114215	in-del	-/AAGA	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:46098487	TTTTTTATGGTTGAG[-/AAGA]AATAGCAGAAATAAA	51317
rs202161942	in-del	-/ACTACTCTAT			intron-variant	PHF21A	GRCh38.p7	11:46107491	TGGTAAAAAACGTTG[-/ACTACTCTAT]AGTTTAAATAAACTG	51317
rs202187902	in-del	-/A	0.0178098	0.0926698	intron-variant	PHF21A	GRCh38.p7	11:46059645	GCCTAGGTTGGTCTC[-/A]AACTGGCCTCAAAGG	51317
rs202204983	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46112757	AACTATCCCCATTTT[-/A]AAAAAAAAGGAACAG	51317
rs202214058	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45981872	CTAAAATCTTTAAGT[-/A]AAAAAAAAAAGTTCT	51317
rs202239805	snp	C/T	0.000562318	0.0167584	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945942	GTCAGGATGACTGGA[C/T]TGGGGGGATGTTGGG	51317
rs367617789	snp	A/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46116916	AGGTTGCAGTGAGCC[A/G]AGATCACGCCGTTGC	51317
rs367649230	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46091782	TGGATGACTTGAATT[A/G]GCTCAAGCCATCCTC	51317
rs367655895	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45974652	TAGAGACGTGATCTC[A/G]CTATGTTGCCCAGGC	51317
rs367656241	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45982503	CTTTCAAGTCTTCAA[A/G]ATTCTATTTCTCCAA	51317
rs367658290	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45947784	ACCAAGCACAAAACA[A/G]AACAAAACAAAACAA	51317
rs367666888	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45962374	TTTACCTTTAGCTCT[A/G]TGATCTATGAGATCT	51317
rs367695317	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46071734	ATATTGATAATAGCC[A/C]AAAAAAAAAACTGGA	51317
rs367705129	snp	A/G	0.000115334	0.00759299	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938253	ACGGGAACATGTGTC[A/G]CACATCAGTAACTGG	51317
rs367708395	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46111028	GACCTCAGGTGATCC[A/C]CCCGCCTCAGCCTAC	51317
rs367726502	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46100331	TCATCAGAGCAGCAT[A/G]GGGTCCCATTAGGCA	51317
rs367735966	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45991209	TTTTTCATGGTTTGA[C/T]AGTTCATTTCTTTTT	51317
rs367743152	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46026010	GATTTTGACAATGTC[C/T]CAAGAATGTCCTTTA	51317
rs367748181	snp	A/G	0.0232847	0.105357	intron-variant	PHF21A	GRCh38.p7	11:45967574	GGTGGCTTTCCCACT[A/G]TCTTAGATAAGGAGC	51317
rs367774347	snp	C/T	1.64741e-05	0.00286998	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971244	CCTTCTGACTGTTGA[C/T]GGCGGTCACCATAGC	51317
rs367795112	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45981525	TAACTATTTGGGGCC[A/G]TATTTGGGCTCTGAC	51317
rs367803872	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45954379	CATCTCACATACACA[A/G]TCTCCTATTTCGGAA	51317
rs367864982	snp	A/G	0.0150606	0.0854603	intron-variant	PHF21A	GRCh38.p7	11:45955248	TGGGTGAAGAGTATG[A/G]TCTAAGCGAGAATCA	51317
rs367871548	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46115715	AAATCAGTTCTAGAT[A/G]TAGATATAAAAGAAT	51317
rs367875584	snp	A/G	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:45966917	CCACTGCACCCAGCC[A/G]TAAGCCAGTATTTTT	51317
rs367877824	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46083397	ACGATTTCAAAAGTT[A/T]ATGTTACCTCAGACT	51317
rs367902723	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46109030	AAAATCAACATGAAA[-/C]CAGCCTCAAAATGAT	51317
rs367940260	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005994	ATGCCTGTGGAAAAG[C/T]ACAATTTTAAACTTT	51317
rs367959632	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45958199	TTTAAAGAATTAGCA[C/T]CAATCTGTCTCAAAT	51317
rs368044954	in-del	-/CTCTCT/CTCTCTCT			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PHF21A	GRCh38.p7	11:46121181	TCTCTCTCTCACTCA[-/CTCTCT/CTCTCTCT]CTCTCTCTCTCTCTC	51317
rs368077380	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46013454	AAGAGTAGTGATGTA[A/G]TATTTTTGGGCCTCA	51317
rs368086043	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46089655	GACCTCCTTAGCTAG[C/T]TGGATGTTTCTATAC	51317
rs368112010	snp	A/C	0.000316427	0.0125743	intron-variant	PHF21A	GRCh38.p7	11:45938318	GAATATCACCCTATA[A/C]AGTTGAGAGGAAAGG	51317
rs368142853	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46051623	TCTCATTAACCAGCT[A/G]TTTTTAAGCATGCCA	51317
rs368170466	snp	A/G	0.00874735	0.0655527	intron-variant	PHF21A	GRCh38.p7	11:46001829	TTTTTAACTAGAGGG[A/G]AGAGGATGGAGGTCT	51317
rs368173029	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45963531	AAGTTTACTCTCTCT[G/T]TAGATTACGGGGAAA	51317
rs368181546	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46020003	GACTCTTTTTTTTTT[-/T]AGCCATCATTATGAA	51317
rs368209804	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46026371	CATGCACAAGGTACA[C/T]GAAAGCTGACAATGA	51317
rs368244343	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975382	TAAAATAAAATAAAA[C/T]AAAACAAAATAAAAT	51317
rs368265106	snp	C/G	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:46053197	TTTCACAGAACACTA[C/G]ATCACATCTCTCATG	51317
rs368269377	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46077950	GCAGTCTCACTCTGT[C/T]GTCCAGGCTGGAGTG	51317
rs368280159	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46092776	TTTTTTTTTTTTTTT[G/T]AAACAATGTCTTACT	51317
rs368286058	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978552	CAACTGAACTATACT[C/T]TTTTTCTCTCTATAT	51317
rs368286196	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46028332	AAATAATAATACTAT[A/G]CATCAAAATGTTAAT	51317
rs368312019	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46063351	TCTCTGGTTAAATTT[A/C]TCTAGAGTAAGATTG	51317
rs368314495	snp	A/G	1.72024e-05	0.00293273	intron-variant	PHF21A	GRCh38.p7	11:45971083	TCCTAACCTTCTCAT[A/G]TGATCACACATGAGG	51317
rs368320207	snp	A/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084821	AGTAGCTGGGACTAC[A/T]GGCACCTGCCACTAC	51317
rs368325596	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967127	TAATCCCAACAATTC[A/G]GGAGGCTGAGGCTGG	51317
rs368337006	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46008971	TGGTTCACATTTCAC[-/T]TTTTTTTTTTTTTTT	51317
rs368350444	snp	A/G			synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935696	TCGTTCTTGTTTTAA[A/G]TCTGAACTCCATTTA	51317
rs368360578	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45990070	ATTTTTCACAGGTGA[C/T]GAAAATTACAAAATC	51317
rs368399176	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46003256	TATAGTGTATGGAGG[A/G]AAGAGCTTGGGTTAA	51317
rs368412505	snp	A/G	0.00914312	0.0669923	intron-variant	PHF21A	GRCh38.p7	11:45946502	CATTCTCCTGCCTCA[A/G]CCTCCCACGTAGCTG	51317
rs368413817	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45995438	TACCTATACTTCACA[A/G]CATGTTTGTGTGACA	51317
rs368418960	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45989325	AAGAAAAGCATGAAC[A/G]ATCTCTTAATGAATA	51317
rs368470297	snp	A/G	0.00017409	0.00932816	downstream-variant-500B, utr-variant-3-prime, synonymous-codon	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928858	TGAGGCTGGGCCGGC[A/G]CTGCCCCTCATCTTA	51317
rs368471718	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46071129	TTTGTCATATAACTT[C/T]GCAAGGCTTGGCCAT	51317
rs368477730	snp	C/T	1.65499e-05	0.00287657	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953583	GGGTGATGGTGCGGC[C/T]CTCTGTTTGTTTCTC	51317
rs368514544	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931923	CCGGCCAAGCCGAGG[C/T]AAGCGCAGCAATTCT	51317
rs368526920	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46020019	AGCCATCATTATGAA[A/G]AGACCTGAATGATGA	51317
rs368545798	snp	C/G	0.000544951	0.0164978	intron-variant	PHF21A	GRCh38.p7	11:45935788	TTTTGACAATTAATT[C/G]TTTGAAATGTCCTCT	51317
rs368556251	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930682	CACTGCCACCAGGGC[A/G]CAGCGCCTGATCAGG	51317
rs368593404	snp	A/G	1.65102e-05	0.00287312	intron-variant	PHF21A	GRCh38.p7	11:46079188	ATAAAGAGAGAAAAA[A/G]AGCCATCAGTCTTAC	51317
rs368638492	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45945514	TCCCAAAACACTGAT[A/G]ATAGAAACCTGCACA	51317
rs368654402	in-del	-/AATAAACACACA			intron-variant	PHF21A	GRCh38.p7	11:46025082	TAGAAACTTTATGAA[-/AATAAACACACA]CTGCCTATCCACAAG	51317
rs368657307	snp	C/T	0.0240643	0.107019	intron-variant	PHF21A	GRCh38.p7	11:46070022	ACATATTAAGTTATT[C/T]AATAATTAAAATCTA	51317
rs368718824	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46034783	TGTGTAAGAAGTCTT[A/C]CATGACCCAGTTTCC	51317
rs368739447	snp	C/T	0.000875616	0.0209055	intron-variant	PHF21A	GRCh38.p7	11:45950328	ATTGCCAGTTCCTAG[C/T]AGGACATTAGGGAAA	51317
rs368743559	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46009464	CCAAGTGTCTGAACC[A/G]TACAATTTAACATCT	51317
rs368747519	snp	A/G	0.000153988	0.00877328	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084204	TAAGAGCCTCCTGTA[A/G]AGTCTGCAACTCCAT	51317
rs368749522	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45964015	ATCAGCTGACCAACA[C/T]GGAGAAACCCCGTCT	51317
rs368750735	in-del	-/C			splice-acceptor-variant	PHF21A	GRCh38.p7	11:45935740	TCTCTTCTTCTTTTG[-/C]TAAAAAAAAAAAAAA	51317
rs368800413	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46063842	TCTGATGAACCCACA[A/T]CATAGGATAAGCAGA	51317
rs368816461	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084860	CATTTTTTTATATTT[G/T]TAATAGAGACGGGGT	51317
rs368844529	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45984768	TGCCCTCCACAACTG[G/T]ATGTCAGTGCTGCAA	51317
rs368850022	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073463	TAAAAAAATTTTTTA[A/T]ATCTTATTTCTTGTC	51317
rs368886127	snp	C/T	1.75647e-05	0.00296345	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965525	CAGCATGACGGGCCT[C/T]TGGATAAGCTGAGGA	51317
rs368897984	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46107888	AAATACTGAGTTATC[A/C]GCATAGCATTTGGTA	51317
rs368938087	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45987554	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	51317
rs368942912	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46058919	GAAAGTCAATCTCTA[C/G]ACAGCAGAAATGAAG	51317
rs368948693	snp	C/T	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:46096109	GAAAAAGCAGAATCC[C/T]GCTTGATAGGCTTAG	51317
rs368968907	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45970785	CACTCAAGTTTCACA[A/G]GAAAACACTGTAGAG	51317
rs368970258	snp	A/C	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46009141	CACCATGCCCAGCTA[A/C]TTTTCTGTATTTAGT	51317
rs368990908	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46059884	GGCACCCACCACCAC[A/G]CCCAGCTGATTTTAT	51317
rs368992522	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45997497	AGCCAGCCCATGCCT[A/G]CGTGAAACAGCTCCT	51317
rs369002359	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46054566	TTTATTAGGGTACCA[A/G]CTAGGGCTGAGAACC	51317
rs369007930	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45948928	TGCTGTTTAGGTATG[C/T]CACTGCACTCTTCTT	51317
rs369008041	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45967340	GCCACTGCACTCCAG[C/T]CTGGGTGATAGAGTG	51317
rs369021883	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086133	ACTATCTTTTTTTTT[C/T]TTTGAGAAAGAGTCT	51317
rs369035329	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46038139	CTCTCTTTTTTTTTT[-/T]AAATGGAGTTTTGCT	51317
rs369043301	in-del	-/CACC/CC			intron-variant	PHF21A	GRCh38.p7	11:46099560	ACACACACACACACA[-/CACC/CC]CACCCTAAACACAAA	51317
rs369045954	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45970892	TCATACTTTGACCTC[A/T]GATAATGCACTGAAT	51317
rs369074726	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45952214	GTGATTCTGTCCAAC[A/T]AGAAGGTGAACTATA	51317
rs369093084	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46053560	ATATGTATACCATGA[C/T]TGGTAAAAAGAACCC	51317
rs369098061	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46021528	ATTGCACATGTGTGT[A/G]CGTGCATGTGTGTGT	51317
rs369108609	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46014382	ATATTCCAGTGTATA[G/T]GCACCACATTTTCTT	51317
rs369111295	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46003818	TGCCCTTCATCAATT[A/G]CTTCCTATGCCAGGA	51317
rs369116906	snp	A/T	0.00010812	0.00735175	intron-variant	PHF21A	GRCh38.p7	11:45945813	TAAGCTCTCAGAAAG[A/T]CAGTGTGCTTTTCCC	51317
rs369162529	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46028852	GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	51317
rs369163062	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45955842	GGAACCTCCAGCCAA[-/C]CAGCCAGTGAAGAAG	51317
rs369187810	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45979517	TTTTGTTATTGACTA[C/T]CTTTCTCCCCTTCTT	51317
rs369192032	in-del	-/AG	0.216349	0.247725	intron-variant	PHF21A	GRCh38.p7	11:46021074	TTAAAAAAAAAAAAA[-/AG]AGAGAGACAAGGTCT	51317
rs369205260	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46086818	GAAATGAACGGCAGG[G/T]TAAAACACAAAGAAC	51317
rs369258051	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078250	TCTCAATTTGTAGAG[A/G]TAAGTGTTATTTTTT	51317
rs369329297	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46029414	CTTCACTGGCTGGGC[A/G]CAGTGGCTCACGCCT	51317
rs369347099	snp	A/G	0.00455331	0.0474966	intron-variant	PHF21A	GRCh38.p7	11:45979732	AGTCTACAATCTGCA[A/G]CCTGCAATGTTCCAT	51317
rs369376668	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005014	TATGGAAAATGAGAT[C/T]ATGCAGTTAAATTTT	51317
rs369380826	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45960279	AGTGGAACCAACCAA[C/T]GTCTTATGATTTCCT	51317
rs369393137	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46079934	TGTCTTTTGACCTAA[C/T]CCAACTTCTAAAGAC	51317
rs369443440	snp	C/T	7.22818e-05	0.00601129	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933953	GATCCCGTGGCTTCT[C/T]CTAGAGGGGCTCTGT	51317
rs369528221	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46054251	AAGTCAGAGTATTAA[A/T]ATGATAGTAACCCTT	51317
rs369529275	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46048780	ATCTCAAAAAAAAAA[A/T]AATTTTTTTTTTGTT	51317
rs369529792	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036248	GTAAAATTTACAGTC[A/G]TAAGTAACATAACTG	51317
rs369539693	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46104191	ATGCCACTTTTATAT[A/C]TCTGGGGTTCTACAA	51317
rs369554287	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45992553	CTCCGTCTCAAAAAA[G/T]AAAATTTTTTGACAT	51317
rs369566250	snp	A/G	0.000437904	0.0147905	intron-variant	PHF21A	GRCh38.p7	11:46079229	CCTATGGCTAATCAG[A/G]TTTGGACCAAAAAAT	51317
rs369574483	snp	A/G/T			intron-variant	PHF21A	GRCh38.p7	11:46014747	GCACTTTGGGAGGCC[A/G/T]AGGCGGGCGGATCAC	51317
rs369596914	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46035031	AAAGAGTAACTAGTC[C/T]ATGAGGACTGAAGAG	51317
rs369606267	snp	C/G	3.29489e-05	0.00405874	intron-variant	PHF21A	GRCh38.p7	11:45949485	TGCTTTGGATTTCTT[C/G]AGAGAAGAAAAGGTT	51317
rs369613756	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45998793	CTGGGATGCTGGGAT[A/T]ACAGGCATGAGCCAC	51317
rs369624628	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46006586	CTGTCTGCCTGAGCT[A/G]GAGGATGAAGTTATG	51317
rs369633006	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45964092	ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAAGGA	51317
rs369648911	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45938689	GAAAACAGAACAATT[A/G]TAACGATATACTGTA	51317
rs369657229	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46113824	GTGAGATTCATTCTC[-/A]AAAAAAAAAAAAAAA	51317
rs369688299	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45992527	CCTGAGCGCTGGGTG[A/T]CAGAGCGAGACTCCG	51317
rs369700401	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46086894	GGCCCTCAAAAATTG[A/G]TAACAAAAATCTATG	51317
rs369720607	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46022016	GTGAAGCAGAGATAA[C/T]TAAGCAATATTTTCT	51317
rs369816781	snp	C/T			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934819	TTTTGCCCTTTTGCC[C/T]TCAGCTTCCCACACC	51317
rs369818959	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46019649	ATGCTTTACTTTTAT[A/G]TTAACTTAAGCAATC	51317
rs369827850	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46103460	TTTAAAAATATTTGT[C/T]GAGCCAAAGTACACC	51317
rs369839675	snp	C/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46091993	CTAGCTGTATTAGCA[C/G]AAACACAAATGCGTT	51317
rs369842313	in-del	-/TATTT	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46080150	CTAAAATATACTATA[-/TATTT]ATCTAACTACTAGTT	51317
rs369847460	in-del	-/AAAAAAAAAA	0.0941369	0.195465	intron-variant	PHF21A	GRCh38.p7	11:45968932	GCGAAACTCCATTGC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA	51317
rs369929052	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45991044	GTCTATTCAGCACAA[C/T]CTTCCCTCACCCTCT	51317
rs369967827	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46020568	TCTAACACCATCTGA[C/T]GATCTAGAATATAAA	51317
rs369971487	snp	A/G	0.000256404	0.0113197	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965340	AGACTTGGCTTGCTA[A/G]GCTGTACAGTTTGAG	51317
rs369977379	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45951585	CCAACTAACTACATT[C/T]CTAATTTTCACTATT	51317
rs370006611	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46035734	GGGAGGAGAACAGTG[C/T]CTCAGAAGGGAGACC	51317
rs370042740	snp	A/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086274	CAGGTGCCCGCCACT[A/G]CACCCGGCTAATTTT	51317
rs370066255	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46015025	AAAAAAAAATAAAAA[A/T]ATAAAAAATAGTTAT	51317
rs370086539	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46026051	AGTCTCAGATCATGC[C/G]AAGTTATCTAAATAT	51317
rs370092547	snp	C/T	0.000122182	0.00781512	intron-variant	PHF21A	GRCh38.p7	11:45969790	CCATCTAACCTATCA[C/T]TGAGCTTGTCATTGG	51317
rs370098777	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46021212	CTACAGGTGCAAGCC[A/G]CTATGCCTGGCTAAT	51317
rs370166935	snp	A/G	0.000153988	0.00877328	missense, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934218	GTGTTCTTCATTTCC[A/G]TGCATTTCTGCAGCA	51317
rs370200588	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46115431	AAATAGTATGGCCAC[A/G]TATACACACAAACAT	51317
rs370209813	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46063468	AAAAGCAGTCAGTCA[C/T]AGAGAATATGTAAAT	51317
rs370218802	in-del	-/C	0.0130921	0.0798413	intron-variant	PHF21A	GRCh38.p7	11:46105389	GGCACACAGGACATG[-/C]CCCTGATGATTAGAT	51317
rs370261903	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46001409	TACTTAGCCAATGCA[C/T]CTGTAGATTCTAATG	51317
rs370313849	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45943109	AGCTATCATCATCAT[C/T]ATCTTTCTTTCCTTT	51317
rs370379618	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46081549	GAGGAAATAAATAAG[A/C]CAATTTTTCTATCTG	51317
rs370381204	in-del	-/CCTAA			intron-variant	PHF21A	GRCh38.p7	11:46099564	CACACACACACACAC[-/CCTAA]ACACAAACACAAACA	51317
rs370421778	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46008446	CTCAGGAAATGGGCA[G/T]CATACATCTCATCTT	51317
rs370430136	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45963380	AGCTGAGATCCCACC[A/G]TTGCACTCCAGCTTG	51317
rs370478347	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46099239	ATCCAGAGAAACACA[C/T]GCACACAAAACAAAA	51317
rs370489997	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46049993	TATTCTATCATATAT[C/T]TCATGTAGTCACCAC	51317
rs370498555	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45967075	TGCTTATGATAAAAA[C/T]GACCCTTTCCTGGCC	51317
rs370500537	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46013247	TGAATAGAAAATTCC[A/G]GAAAAAATAATCCAT	51317
rs370521561	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46007405	TGCAACCTCCACCTC[C/G]CAAGTTCAAGTGATT	51317
rs370531446	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45982713	CATCAAACATATTAA[C/T]GAACTAGCTAACGTG	51317
rs370531602	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093070	CACATCTTACCACTT[C/T]AGATTGTAAACCACA	51317
rs370532961	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46088203	AAGTTATAAATAACA[A/G]ATCAGTTGCTGCAAA	51317
rs370533546	snp	A/G	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46032000	AACATGAAAACCACA[A/G]CTTTATTAGCTGATA	51317
rs370571661	snp	A/T	0.000270453	0.0116255	intron-variant	PHF21A	GRCh38.p7	11:46076856	CTGTGAGAAAGATAT[A/T]TCATTTGTTAACAGA	51317
rs370571667	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45985428	AACAAAAACACAGAA[C/T]GCCATTTTATGGACA	51317
rs370609907	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45966198	ATGTACTGAAGACTC[A/T]CACTTTTACCTCAGA	51317
rs370612753	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45994213	GGCAACATTTAGACT[A/G]GGTAAAGTGTTGGGC	51317
rs370621699	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929938	GCAGAGGGACAGGGG[C/T]GAGGTTCACACAGAG	51317
rs370627435	snp	C/T	0.000148352	0.00861127	missense, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934143	ATGCCGTGGATGAGG[C/T]GAATCAGCTGTTTTA	51317
rs370632163	in-del	-/TTTAA			intron-variant	PHF21A	GRCh38.p7	11:46007718	ATTTAGTTACATTAA[-/TTTAA]ATCAAAAAACGATGT	51317
rs370685997	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46069794	TGCACTTGTGATTGA[G/T]TTAAATGTTAAATGT	51317
rs370718662	snp	C/G			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122353	CCCGGCCGCCGCTCG[C/G]CCGCTCCCTCCCCTC	51317
rs370729723	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46023940	CATCCTGGGCGACAC[A/G]GCAAGACACCATCTC	51317
rs370836454	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46105455	GTTAAGAGCCCCCAG[A/C]CCACCTTTCTCCACA	51317
rs370861807	snp	A/G	0.0232847	0.105357	intron-variant	PHF21A	GRCh38.p7	11:46030715	CACATTTGCATTCAA[A/G]TATTTTATGTTCCCA	51317
rs370868329	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005553	ATAAAACAGGTTATT[C/T]TGACTCCATTAGCAA	51317
rs370872317	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055799	ATTGAAAATATAATA[C/T]GATCTAAGCCTAAAA	51317
rs370876373	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45994949	TATTTTCAACCAAAG[G/T]ACGTAAGAATCTAAC	51317
rs370877031	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972764	ACTAAAAATACAAAA[A/C]TCAGCCAGGCCTGGT	51317
rs370877032	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46017073	CCTCCCAGGTTCCAG[C/T]GATTCTCCTGCCTCA	51317
rs370907044	snp	A/G	1.6966e-05	0.00291251	intron-variant	PHF21A	GRCh38.p7	11:45934242	TGCAGCAAATGACAA[A/G]GGCAGTGGCACTGAG	51317
rs370921832	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46033334	CAGTGGTGCAATCAT[C/G]GCTCACTGCAGCCTC	51317
rs370964585	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46091054	AAAGGCAAGTAGAAT[-/A]AAAAGGTAGTAAATG	51317
rs370966395	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46043740	AACATTCCATCCTGA[A/C]TGCAATGTCTGCATC	51317
rs371059162	snp	A/C	1.70886e-05	0.00292301	intron-variant	PHF21A	GRCh38.p7	11:45971090	CTTCTCATGTGATCA[A/C]ACATGAGGAGCAGCT	51317
rs371126612	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45979417	CCAGAAGAGGTCAAG[A/T]CACAAACTTTTAGAA	51317
rs371144813	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45935303	AGTGTCAGGTGAGGC[A/G]CTACACTCCCCCCAC	51317
rs371197688	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45987237	GGCAACAGAGCGAGA[C/T]TGTATCATAAATAAA	51317
rs371203874	snp	C/G/T	0.000121654	0.00779832	intron-variant	PHF21A	GRCh38.p7	11:45953492	ATAAACCATACACCA[C/G/T]AGACTGAGACCTGCC	51317
rs371211882	snp	A/T	1.64746e-05	0.00287002	intron-variant	PHF21A	GRCh38.p7	11:45949367	ATAAATAAAACTGGA[A/T]CATGAGGGAAGGGCC	51317
rs371213531	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116263	TCTAAAATAGAAAAA[A/C]AAAAATGATATATCC	51317
rs371232600	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46070174	AACTAGTTATAGGAG[A/G]GACAGAAACTTCTTT	51317
rs371265768	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46116927	AGCCGAGATCACGCC[A/G]TTGCACTCCAGCCTG	51317
rs371302419	snp	A/G	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971279	GTAGGTCTCTGGCCC[A/G]CCACAGAGGCAGGCA	51317
rs371310181	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45991115	TTTCCAGAATGTCAT[A/G]GAGTTGGAGTCATAC	51317
rs371327409	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46074541	GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	51317
rs371372891	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45976431	TGCACACAGTAGGAA[C/G]TCCACAAATATTTAC	51317
rs371380766	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46001094	AACATATCTTAACCA[C/T]AAAATCAGACATTTT	51317
rs371399534	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46022489	AACAAAAAGACAGGG[A/T]CTCCCTTTGTCACCT	51317
rs371422108	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46046041	ATCTTCAGAAATGCA[A/G]TTCTCAGCTTTGTGA	51317
rs371447807	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46039243	TGTTTTCGTGCATTC[A/G]CTGTTTTAGTATAGG	51317
rs371455070	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46014295	CTGCATTAATTCCCT[G/T]AGGATAATGGCCTCC	51317
rs371467875	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46082415	ATCAACAATCGTGTA[A/G]GTGACACCATATAAA	51317
rs371476255	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45991636	TAGAGAGGCAGTATT[G/T]TGCTGTAAAAATAAT	51317
rs371518017	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46023146	ACAATTAGAAAAAAA[-/A]GAGAGGAAAAGTTAA	51317
rs371576180	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46052825	TTCTTGGACATCTCT[A/G]ACCAAGCCATCTTAC	51317
rs371592042	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46002529	ACTATTTGGGGGAAA[A/G]AAAAAGGAATTCACA	51317
rs371597267	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46012206	CATCTATCCATTTCC[C/T]TCAGAAAGTATTCAA	51317
rs371599704	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978157	ATACAAAAATTAGCC[A/G]GGCATGGTGGCACGC	51317
rs371604835	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46026765	TCTAACGTGCACAGA[C/T]AGCCAAAAGGTACTG	51317
rs371610672	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45955752	AGGGTGTCTTTCCTT[A/C]GTGGATCTCTTGCTC	51317
rs371624294	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45957816	AAATGAAATAGAGAA[C/G]AACAACAGACTCAAC	51317
rs371625119	snp	A/G/T	4.94501e-05	0.00497223	missense, synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938214	TGTTTTCAGAGGGGG[A/G/T]TCTAAGCAGTCCAAA	51317
rs371629369	snp	C/T	1.6528e-05	0.00287467	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945953	TGGATTGGGGGGATG[C/T]TGGGGTAAGGGCTCC	51317
rs371635524	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46065607	AAACTACAGCTAAAA[A/G]CATCTGTACTGATAC	51317
rs371651231	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46014756	GAGGCCGAGGCGGGC[G/T]GATCACGAGGTCAGG	51317
rs371670725	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45968415	TCTAGCCTGCATGAG[C/T]CACATGGCCCTCTGT	51317
rs371677855	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46086775	AGTAACATAAAACCA[C/T]AGTTCAATTCAATTC	51317
rs371707698	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45934549	AAACAAAGGTTGTTT[-/A]AAAAAAAAAAAAAAG	51317
rs371713739	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45975832	TATGCCAATCACCCG[A/G]CTTAGAATAAAAAAC	51317
rs371771370	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46046791	AAGCCTGCCTTCACT[C/T]TGTGAAGAGTGTCTG	51317
rs371783717	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46034964	CATTCTCTGCCACAC[A/T]GAGTTAGCCTACCGT	51317
rs371795100	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084516	CAAAAAAAGGGTTTA[A/G]TCTGGTCATGGAAAC	51317
rs371796490	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45950008	GGGAGGTTTTCCCAG[G/T]ACAGTAGTGTGGATA	51317
rs371802787	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975322	CTGTCTCAAAGAAAA[C/T]AAAATAAAATAAAAT	51317
rs371834902	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46091150	AGACACCACAAGCAC[C/T]ATAAACTATCAAAAG	51317
rs371839102	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46111330	TAACAATTAGCCAGG[C/T]ATGGAGGTGCATGCC	51317
rs371895408	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46041338	ATTTAGGATGTTCAA[G/T]GAAATTACTATGTCA	51317
rs371902130	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45998391	CAATATTAAATGAAT[A/G]TGCCTACTGAGTATA	51317
rs371902663	snp	C/T	1.65187e-05	0.00287386	intron-variant	PHF21A	GRCh38.p7	11:46079214	CTTACATATTAACTC[C/T]CTATGGCTAATCAGG	51317
rs371914854	in-del	-/T/TT	0.204496	0.245824	intron-variant	PHF21A	GRCh38.p7	11:45951807	CTCTTGTGGAATAAA[-/T/TT]TTTTTTTTTTTTTTT	51317
rs371928393	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45995253	CCACTTTTGCCACTA[A/G]TCATAGGGGAGAAAG	51317
rs371930578	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45941311	CCCTTTATTACCCAG[-/G]CTGGTAAAAACTTTC	51317
rs371948562	snp	A/G	3.31389e-05	0.00407042	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945892	ACAGGTGCAGGGAAA[A/G]TGAATGTGGTCTCTG	51317
rs372019328	in-del	-/GTGT			intron-variant	PHF21A	GRCh38.p7	11:46021556	TGTGCATGTGTGTGT[-/GTGT]TCAGAGACAGGGTCT	51317
rs372037631	snp	A/G	9.90197e-05	0.00703563	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979805	AGCTGACTGCTGGGC[A/G]TGGTGGTGGTGGTAC	51317
rs372053712	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46040256	ATAATGGTCTCACCT[C/G]AGTGGAAAAGAGAGG	51317
rs372061206	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46107020	TCCAGCTGTCCCCAC[A/G]GCTGCCTCTTCTGCA	51317
rs372073213	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46084004	TCTTAAAAGCAGTAT[C/G]TATGACTTTGTCGAG	51317
rs372078936	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45989158	ATGTGATAAAGGATA[A/C]TTTGCACTTCTCTGT	51317
rs372101919	snp	A/G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46020416	TCGATGGGTCTTTGC[A/G/T]CAGCAGCAGGAGGGA	51317
rs372103482	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46096928	CCTCAGAGTCATTCC[C/T]ATCTCAGTAAATGGT	51317
rs372110559	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46117876	CAAAGACTTCACTTT[C/G]AAGTAGCAAACATTA	51317
rs372115450	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46059374	GAAATGCTCAAGATA[C/T]AGACAAAATAAGTAT	51317
rs372120817	snp	G/T	1.78595e-05	0.00298822	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965539	TCTGGATAAGCTGAG[G/T]AGCTGCGAGCATGGG	51317
rs372141991	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45974166	AGGCACAAGACCTAG[C/T]ACTGTATGCTTCAGT	51317
rs372156698	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46070534	CAGGGTTTCGCCATG[C/T]TGGCCAGGCTGGTCT	51317
rs372165215	in-del	-/CTA	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46058153	ACACCTCCCTACATT[-/CTA]CTGCTGCCTTACCAT	51317
rs372169222	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46018958	CATACCGTAAGCAGC[A/C]AGAACACACACATCA	51317
rs372191623	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45974689	AGAACTCGCTCTCAC[A/G]TAATCCTCCCACATC	51317
rs372203435	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45958810	ATAGTCCTAGTTACT[G/T]GGGAGGCTGAAATGG	51317
rs372225934	in-del	-/A/TA	0.39536	0.203397	splice-acceptor-variant	PHF21A	GRCh38.p7	11:45935741	TCTTCTTCTTTTGCT[-/A/TA]AAAAAAAAAAAAAAA	51317
rs372240747	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46059407	CTAAAATAATAAGTA[C/T]AATACCAATCTCAAT	51317
rs372245110	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46026241	TGACTAAGTTTTAAA[A/G]TTAAAATTCCACCCC	51317
rs372256396	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46058965	ATGAAGAGACACAAG[A/T]GACAGAGACTCCAGT	51317
rs372273429	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46009424	GACTCTACCTGCCTA[A/G]AATGATCTGTGAAAC	51317
rs372279969	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46078000	CACTGCAACCTCTGC[A/C]TCCCAGGTTCAAGTG	51317
rs372287878	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46047156	GGACCCAGTCTGAGA[G/T]AAAGGCTTCAGGCAG	51317
rs372293640	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46028556	AAAATATTACTTTAT[A/G]CTTTAAAAGCTTGCC	51317
rs372315125	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46008180	ATTTGTTTACTCACA[C/T]ACGCCCATACACTCT	51317
rs372351634	snp	A/T	0.000307953	0.0124049	intron-variant	PHF21A	GRCh38.p7	11:45953668	CAGAATTCGTTTTTT[A/T]TTAAAAGGATGAAGC	51317
rs372360418	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46038761	TTCTCTTCCTTTTCT[C/T]ATAAAACCACTAGTT	51317
rs372455906	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45943488	GCCTGCCCATCATCA[C/T]CTCTTGCCTGGACAA	51317
rs372471352	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45979659	ACTTTTGTTTAGTTC[C/T]AGCTGAGCTTAGTAT	51317
rs372486510	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975387	TAAAATAAAACAAAA[C/T]AAAATAAAATAAAAC	51317
rs372531905	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116276	AACAAAAATGATATA[C/T]CCATATATACCTAAT	51317
rs372583940	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46008160	CACCTTCCCCTACAA[C/T]GTGTATTTGTTTACT	51317
rs372617550	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46114293	ATACAGTTGCTACAC[A/C]CCCTCCTATTTTCTG	51317
rs372644822	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46092005	GCAGAAACACAAATG[C/T]GTTTGAAGTATAGCT	51317
rs372660566	snp	C/G/T	0.00398731	0.0445001	intron-variant	PHF21A	GRCh38.p7	11:45989407	TGCCTATAATCCCAG[C/G/T]ACTTTGGGAGGCCGA	51317
rs372668531	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45971736	TTGCTGTCAATTAAT[C/T]TAAACTTTGTACTAG	51317
rs372688832	snp	C/G	0.000131981	0.00812237	intron-variant	PHF21A	GRCh38.p7	11:46076740	AAATATGCCCCCCTC[C/G]CCTTTTCCCCTACCT	51317
rs372697888	in-del	-/AAG			intron-variant	PHF21A	GRCh38.p7	11:45955009	ATGATTACATAAAGA[-/AAG]CGTAAGCATCTGCCT	51317
rs372719754	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46031124	GCCACCCAAGCTCAA[A/T]GCCTCAGAGTCACTT	51317
rs372727495	snp	C/T	0.0154538	0.0865337	intron-variant	PHF21A	GRCh38.p7	11:45974001	CACCTGAATTATATA[C/T]TTACCATTAACCCAA	51317
rs372736162	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931973	GGCTTGTGGGTGGGT[A/G]GAGTGGAGTAAATTT	51317
rs372738577	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45995458	TTTGTGTGACAGTTA[C/T]ACTGTCATAATTTTA	51317
rs372741151	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085441	AATTTAAATTATTTC[A/G]ATGGCTAATTTATCC	51317
rs372760074	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46032531	TAATGAACATCCTTA[A/T]AAATGTATCTTTATT	51317
rs372765921	in-del	-/CTTA			intron-variant	PHF21A	GRCh38.p7	11:46027328	TCTGCCATCGTTTAC[-/CTTA]TTTATACATGTATAA	51317
rs372774959	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46015026	AAAAAAAATAAAAAA[A/T]TAAAAAATAGTTATT	51317
rs372785569	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946836	ATGAGGGTGGAGACC[A/G]GCAAAGCAAGGAGGC	51317
rs372785710	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46104238	TTACACCCAAGCATG[A/G]GTTCTCAAGGGTTAA	51317
rs372818813	snp	A/T	1.88831e-05	0.00307265	intron-variant	PHF21A	GRCh38.p7	11:45946132	TGAGGTAGCAGACAG[A/T]AGGTTAATTCAACAG	51317
rs372848607	snp	A/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PHF21A	GRCh38.p7	11:46121110	CTTTTTAGATATTAG[A/T]GTGTTAAGATGGTAG	51317
rs372850156	snp	C/G	4.95446e-05	0.00497693	intron-variant	PHF21A	GRCh38.p7	11:45936585	CTGAAAAGATTTTTA[C/G]AATTTTACCTTGAGA	51317
rs372853435	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45967229	GAACATTAGCCAGGC[A/T]TGGTGGCACACACTT	51317
rs372866292	snp	A/C/T	0.000148873	0.00862648	intron-variant	PHF21A	GRCh38.p7	11:46076719	ATCTTTAGAACACAA[A/C/T]GTTAAAAATATGCCC	51317
rs372880875	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45937641	GCCTGCCACCATGCC[C/T]GGCTAATTTTTATAT	51317
rs372883088	in-del	-/A	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45949215	TCTGCTGAAACTTAG[-/A]GAAAAAAACCTAAGG	51317
rs372890358	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46010074	CTTAACCATATCATA[C/T]TAAAAGAAAGGGGAG	51317
rs372903695	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45977433	TGTGCCACTGTGCCT[A/G]GCCTCCTTTGATTTT	51317
rs372917577	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45999906	GTGGTGAACAGGAAG[A/G]CTTGTCTTATCCTCT	51317
rs372929348	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45952521	CTCAGAGCATAATAC[C/T]TGTCATTAATTCTGT	51317
rs372945539	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45958305	AGAAAATGGGCTGGG[C/T]GTGGTGGCTCACTTT	51317
rs372948747	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46004632	TCTTATCAAACAAAA[A/G]CTCACTTTTCTTCAT	51317
rs372978240	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45946184	CAAAGATTTAAATGT[C/G]ATTAGAAACAACTAT	51317
rs372985613	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46113552	TTAATTGTTTTGGCC[A/G]GGCGCGGTGGCTCAC	51317
rs373010140	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45985465	CAGAAGAGAAACTCA[A/G]GATAAACTCCCTCCT	51317
rs373013037	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45986456	GAGATGTGACCCCTA[C/G]AGAATTACAGATTCT	51317
rs373014908	snp	C/T			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935091	CAACCCTCTTTCCCA[C/T]TTGGACAGGCCGGGC	51317
rs373094874	in-del	-/AAAAAAAAAAAAA			intron-variant	PHF21A	GRCh38.p7	11:45968945	GCAAAAAAAAAAAAA[-/AAAAAAAAAAAAA]TAGGCAGGTATCCCT	51317
rs373186108	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46103596	ACACCTATTCACCTA[C/T]TAGACCTTTATCAAA	51317
rs373217561	in-del	-/A	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46024376	TTTCTGCTTGTTATT[-/A]AGCAACATCACTTTT	51317
rs373246171	snp	A/G			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122656	TTTTATGCCTATTCT[A/G]CCTCCAAGGACTGTA	51317
rs373259563	snp	A/C			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084825	GCTGGGACTACAGGC[A/C]CCTGCCACTACGCCC	51317
rs373263569	snp	C/T	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46074222	TTTTCTAATAAATAT[C/T]GAAAAAAATGATTAC	51317
rs373268719	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46087157	TTGATATTTTCAAAA[C/T]TTTCCATAAAAAATA	51317
rs373311808	in-del	-/GAGA			intron-variant	PHF21A	GRCh38.p7	11:45996523	AGACAGAGAGAGAGA[-/GAGA]AACGTATTCCATTAA	51317
rs373332045	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45939845	GCCTAGCTCATTCTC[A/T]GGATGGGATTAAATC	51317
rs373348305	snp	C/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:46061214	GTCACTGTGACCCTG[C/T]AGTATAGTTTGAAGT	51317
rs373358744	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45961679	GGGTGGCAGTGGGGT[A/G]GAGAAGAAACATAAT	51317
rs373361755	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46048104	CATTGCCACTGCCCC[A/G]AAAAGGAACTCTGTG	51317
rs373380528	snp	C/T	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:45966324	AATCTTCTCTTCCTC[C/T]GATAATTGCCTCAGT	51317
rs373392576	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46021120	GTGGGAGTGCAGTGG[C/T]AGGATCATAGCTCAC	51317
rs373397587	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45987285	GTATGTATGTATGTA[A/T]CCTGACCCATCAAAG	51317
rs373398246	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45975575	AAAGGTTTGTTTTCC[A/C]TTTGGTTTTATTAAC	51317
rs373408515	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45981393	GTGAAACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	51317
rs373411765	snp	C/T	0.000155233	0.00880864	intron-variant	PHF21A	GRCh38.p7	11:45934259	GCAGTGGCACTGAGC[C/T]GCCTGGTTTCTAACA	51317
rs373430160	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984384	ATTCCCTTGACATTC[A/G]CATCACTGGGTTTCA	51317
rs373473917	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45961419	TATTTTCTCTACTAT[C/T]GCACCAGTATTAAAA	51317
rs373476834	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46063499	GTAAAGAGTGTGATT[G/T]TGTTCTAATAATTTT	51317
rs373489676	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992779	ATATACAAAATATAA[C/T]AGTGGAAATGAAAAT	51317
rs373490461	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45964272	AAGCACTTCCTGGGG[C/T]TTGAATAGGTTCCCC	51317
rs373505398	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45969753	ACAGGCTACTTAGAA[A/G]GAGCCCATGAGGATT	51317
rs373514109	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45941251	CTACAAGTGCGTACC[A/G]CCATGCCCGGCTAAT	51317
rs373530483	snp	C/T	4.94376e-05	0.00497156	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946038	AACAAAAGGGAAAAA[C/T]GGGGAGGGAAAGAGA	51317
rs373608817	snp	A/G	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:46073315	CCTGGGCAACAAAGC[A/G]AGACCCCGTCTCAAA	51317
rs373632652	snp	A/C	3.42777e-05	0.00413977	downstream-variant-500B, missense, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928823	CAGCCCTGCAGCAGC[A/C]CCAGAGCCCTGCCCG	51317
rs373638104	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46055512	AGACTTTGCTCTCCA[C/T]AGAGCTTTTACTGTT	51317
rs373664975	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005028	TTATGCAGTTAAATT[C/T]TAACACATGCATGTA	51317
rs373758304	snp	A/C	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46011382	TAATCCCAGGTACTT[A/C]GGAGGCTGAGGCAGG	51317
rs373760013	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46054735	AAGAGAAGCTTTTTC[A/C]GCCTTGTTCATCACT	51317
rs373761230	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45972730	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC	51317
rs373767892	snp	A/G	1.65051e-05	0.00287267	missense, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934119	GAGTCTACAGGTTTG[A/G]AGAGGTCGATGCCGT	51317
rs373807447	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46031755	ATAGTGTCTGGAAAA[G/T]AATGCAATAATTTTT	51317
rs373829450	snp	A/T	0.000153988	0.00877328	intron-variant	PHF21A	GRCh38.p7	11:46079187	AATAAAGAGAGAAAA[A/T]GAGCCATCAGTCTTA	51317
rs373842915	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46009931	ACAGATAAAGGGGCC[A/G]TCAGTCACTTTACAG	51317
rs373855533	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953559	GTTTTGGTTTGGGTG[C/T]AGCAGGTGGGGTGAT	51317
rs373895637	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933700	AGAGAGAGTAAATAT[A/G]TTATTTCACTTGGCA	51317
rs373913532	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017979	TCCTAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	51317
rs373915657	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45972769	AAATACAAAAATCAG[C/T]CAGGCCTGGTGGCAG	51317
rs373917182	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058256	CCAATCATTTACTTA[C/G]AAAAAAATGAATGGT	51317
rs373917512	snp	G/T	1.64817e-05	0.00287064	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979830	TGGTACTGCTGCTGT[G/T]GTTGTAGTTGCTGTA	51317
rs373924016	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46105625	CACCATAAAAAAAAA[A/C]ACAAAAGGAATGAAT	51317
rs373930757	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45969761	CTTAGAAAGAGCCCA[C/T]GAGGATTTCTGTCCC	51317
rs373937785	snp	A/C	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46032160	CCTTAGTTAGGATCA[A/C]CCTGCTACACAAAAT	51317
rs374017792	snp	C/T	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:46062664	TTGGCTATGTTCATA[C/T]TTAAGATTGAAGCGC	51317
rs374028720	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46088455	CATAAAAACCAAACA[C/T]ACAAACCAAACACAC	51317
rs374041035	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46037543	CTACTTGGGAGGCTG[A/G]GGCAGGACAATCGCT	51317
rs374043812	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45989472	AACCTGGCTAACACG[A/G]TGAAACCCCATCTCT	51317
rs374045572	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46012356	CTTCTTAGACCCTTT[C/T]ATATTCAGATGCTTT	51317
rs374073550	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46117567	TCCGAGGGGAAAAAA[-/A]CTACAAGAAGTCTAA	51317
rs374137701	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930491	GGCCTGATAAGGAAG[A/G]AAGAAATCAAAACCC	51317
rs374147814	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46064526	ACTTTGGGAAACATA[C/T]CTTCTGAAAACATAA	51317
rs374156740	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45974090	TTTATTTTACAACTA[C/T]GGTTATGGCTGATTT	51317
rs374227904	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036364	TGGGCAGCTGGGCTA[G/T]AAATGTAACATTCTC	51317
rs374261564	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46058787	ATTCTCTTTACAAAA[C/T]CTGGAACAAGAACAA	51317
rs374279867	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084618	CACTTCTGTCTTCAA[C/T]GAGACTATAACCATC	51317
rs374384809	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46089585	CCTGATTTTCGAGGC[A/G]AACCCTCTGAATGTG	51317
rs374415498	snp	A/G	6.95725e-05	0.00589758	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965519	CTTGGTCAGCATGAC[A/G]GGCCTCTGGATAAGC	51317
rs374419930	snp	C/T	3.43083e-05	0.00414161	intron-variant	PHF21A	GRCh38.p7	11:45969802	TCATTGAGCTTGTCA[C/T]TGGTTTACTCACCTG	51317
rs374421429	snp	A/G/T	0.00170267	0.0291291	intron-variant	PHF21A	GRCh38.p7	11:45971065	ATACTATACAAATGC[A/G/T]TATCCTAACCTTCTC	51317
rs374426147	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46025127	CTTTCTCTGAAAGAG[A/G]TAACAGTGACAGGAA	51317
rs374432074	snp	A/G	1.6966e-05	0.00291251	intron-variant	PHF21A	GRCh38.p7	11:45971095	CATGTGATCACACAT[A/G]AGGAGCAGCTGCTGG	51317
rs374459075	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46056968	AGCTTAAAGATAACT[G/T]ATTTTATTTGCTTTA	51317
rs374478762	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45974073	TAGGTTAGCAGTTTT[A/C]TTTTATTTTACAACT	51317
rs374481302	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46007072	CATTACAAAAACACT[G/T]AAATATAGAGTGACT	51317
rs374485340	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46100204	TTGATATTAATGCTA[G/T]CCTTTAAGACCAAAA	51317
rs374507344	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46056210	TTTTTTTAAGTTAGA[C/T]AGCAATTTAGCAATT	51317
rs374553564	snp	G/T	3.41058e-05	0.00412938	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934023	CTCTGGGAGGAGGGG[G/T]AAGGGGCCGGCGTGG	51317
rs374562531	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45970465	GCCATTTTAAGGGAA[G/T]TTTACATCAAAATTT	51317
rs374563798	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45957770	AAAAAAAAAAAAAAA[-/G]AAAAAAGAAAATAAA	51317
rs374564197	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45974228	ATTGACACCAAGACC[A/C]AGGTAGTGCTTAGAT	51317
rs374565849	snp	C/T	9.21893e-05	0.00678868	intron-variant	PHF21A	GRCh38.p7	11:45965272	AGCCATATGCCTCAA[C/T]GACAAGGCTACTGCC	51317
rs374568278	snp	C/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931796	AGGGGCACGCAAGGG[C/G]CAAAGGTCTCCAGCG	51317
rs374586100	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934144	TGCCGTGGATGAGGC[A/G]AATCAGCTGTTTTAC	51317
rs374612816	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46043436	TGGTTAACATACTAC[C/T]TTCTATATCTAGAAA	51317
rs374662224	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45944447	TTTCAAAATAAATAC[C/T]GAAAAATTATGTCAC	51317
rs374696601	in-del	-/TT			intron-variant	PHF21A	GRCh38.p7	11:45940656	TTTCTTCCTTCATTA[-/TT]TTAAAATCAGGCTGA	51317
rs374699916	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45963033	CGACAGGAAAAGATG[C/T]TTAAGATCTATTAAA	51317
rs374733403	snp	C/G/T	0.000627925	0.0177081	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928854	AGGCTGAGGCTGGGC[C/G/T]GGCGCTGCCCCTCAT	51317
rs374764283	snp	A/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45991370	TTACTTGCCAGGTAG[A/T]ACAATGAGGCTCTGA	51317
rs374768210	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46021491	ACCAAGGGTGCCACA[A/G]AAAGCAATCAAAGAG	51317
rs374773338	snp	A/C			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120218	CCAGATCCCTCAGTC[A/C]ACAAACAAGATGGTT	51317
rs374786118	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46098509	AGCAGAAATAAATAG[A/G]AAGAAGAAATCTTGC	51317
rs374787647	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46073389	ATTTAATACCATGAG[A/G]AGAATGTCATTAGAT	51317
rs374820378	snp	C/T	0.000294367	0.0121284	intron-variant	PHF21A	GRCh38.p7	11:45935769	AAAAAAAAAAAGGAA[C/T]GGTTTTTGACAATTA	51317
rs374841336	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45963439	AAAAAAAAAAAAAAA[-/G]AAAAGAAAAAAAAAT	51317
rs374916339	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46055048	ATCTACAGGTTAGAG[C/T]GCCAAAACGTCTTTC	51317
rs374935586	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46092910	CTTCAAGTGTGCCAC[C/T]ATGCCTGGCTATTAC	51317
rs374945142	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46096545	TTGACCCACTGCTCA[C/T]TTCTTCCTCCTCAAA	51317
rs375030687	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45956792	TATACAGAAAACAAA[C/T]AGCAAAATGGCGTAA	51317
rs375036326	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987931	CTCCCATTCCTCTGC[A/T]CTGTAGCTGCTGTGG	51317
rs375040302	snp	A/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086125	TTTTAGCTACTATCT[A/T]TTTTTTTTTTTGAGA	51317
rs375044805	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974620	TACCACACCTGGCTA[A/T]TTTTTTTTATTTTTA	51317
rs375074054	in-del	-/TA			intron-variant	PHF21A	GRCh38.p7	11:46108568	AAATGTGTGTGTGTG[-/TA]TATATATATATATAT	51317
rs375091067	in-del	-/A	0.436692	0.166271	intron-variant	PHF21A	GRCh38.p7	11:45992376	CTATACTAAAAATAC[-/A]AAAAAAAAAAAAAAT	51317
rs375136947	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46071107	TTAAAATTATACATT[C/T]ACACCCTTTGTCATA	51317
rs375145030	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46072670	TGAGATAATAATAGA[A/G]ACAGTTGATTTTGAC	51317
rs375146676	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46047364	CCTTGATGGTTTATC[A/G]TGAAGCATTTTTATA	51317
rs375165976	snp	C/T			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123154	GCAACAGTGGTGAGA[C/T]GATTTGCCCAAAGTC	51317
rs375167458	snp	A/G			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934715	AGCAGGAAGTGAGAC[A/G]ACAGGCCAGCAGCAT	51317
rs375180158	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45974704	GTAATCCTCCCACAT[C/T]GGCCTCCCAAAGTGT	51317
rs375203423	snp	G/T			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46088581	TCACTGTGTGACTAC[G/T]CTCATCCCCAGGGTT	51317
rs375227546	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46053123	TTTTCAATTCAAAAT[G/T]TGTAATTAAATGTAA	51317
rs375246425	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46060383	AATATTCTAGTCTCC[G/T]CCTACAGCTCTAAGA	51317
rs375260855	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45968032	GACTAAACCTTAGAT[C/T]CCTTACCCTAAAAAG	51317
rs375262339	snp	A/C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938083	GACTGCCATTTCCCC[A/C/G]GGAAAGGAATTCCTC	51317
rs375277440	snp	C/G	3.29506e-05	0.00405884	intron-variant	PHF21A	GRCh38.p7	11:45948842	AAACACACACACAAA[C/G]CAAAAGCAACAGCAG	51317
rs375277864	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45945336	GTATTTGACAGTTTT[C/T]CCGGAACCTGTTTCT	51317
rs375291032	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46054025	CGCCACAAGCTTTTT[C/T]ACAAGCAACGTCGTG	51317
rs375318501	snp	A/G	5.05983e-05	0.00502957	intron-variant	PHF21A	GRCh38.p7	11:45938328	CTATAAAGTTGAGAG[A/G]AAAGGTAAGAAAAAG	51317
rs375353258	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967126	GTAATCCCAACAATT[C/T]GGGAGGCTGAGGCTG	51317
rs375367359	snp	A/G	0.000153988	0.00877328	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946008	TGGAGGACGACCTAT[A/G]TACCAAGAGAAGGGA	51317
rs375369650	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45995427	ACAGGGGTGCATACC[C/T]ATACTTCACAGCATG	51317
rs375439396	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46001356	CACTAGATATCACTG[C/T]TATCAACAAATTTCT	51317
rs375462362	in-del	-/GC	9.25134e-05	0.0068006	splice-acceptor-variant	PHF21A	GRCh38.p7	11:45935739	TTCTCTTCTTCTTTT[-/GC]TAAAAAAAAAAAAAA	51317
rs375466721	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46080955	AGGCGTAAGCCACCA[C/T]GCGCAGCTCTTGCTA	51317
rs375495711	snp	A/C/T	3.30246e-05	0.0040634	missense, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934191	TGCATCTCCTTCTGC[A/C/T]GGGCCAGGATGGTGT	51317
rs375497452	snp	A/C/G	9.01091e-05	0.00671175	intron-variant	PHF21A	GRCh38.p7	11:45935770	AAAAAAAAAAGGAAC[A/C/G]GTTTTTGACAATTAA	51317
rs375519571	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116014	ACTTTCTAAAGGGGG[A/C/T]AATTTCAAAAGAATA	51317
rs375633001	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45992328	ATGAGGTCAGGAGAT[A/C]AAGACCATCCTGGCT	51317
rs375654133	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46068554	GATATGTTCTATGCA[A/G]AAGAAAAAAGACAGA	51317
rs375659188	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46092159	GGATCAGGCACACGA[C/T]GTCTACCTAGTCAAA	51317
rs375664047	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45984190	AAAAGAAAGCTGGAA[A/G]GAACAAAGACGGAAG	51317
rs375722056	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46113551	TTTAATTGTTTTGGC[C/T]GGGCGCGGTGGCTCA	51317
rs375739459	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46011984	CCAGATGACTATCAC[A/C]TTCTTTACTTCCTGT	51317
rs375747597	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46036960	AGGCAATCCTCTCAC[C/T]TCAGCTTCCCAAAGT	51317
rs375764059	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46043415	TTTCCTCAAATTAAT[A/C]CTTTCTGGTTAACAT	51317
rs375764745	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45935915	TTCTGTGTACAGTAT[A/G]CTAAAACTGTCAGTG	51317
rs375770563	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45984621	AGTCACGTTCCATGG[C/G]TTTTGTCAACAGAGA	51317
rs375773738	snp	C/T	1.64993e-05	0.00287218	intron-variant	PHF21A	GRCh38.p7	11:46076737	TAAAAATATGCCCCC[C/T]TCCCCTTTTCCCCTA	51317
rs375815592	snp	C/T	1.64741e-05	0.00286998	intron-variant	PHF21A	GRCh38.p7	11:45979749	CTGCAATGTTCCATC[C/T]ACACATTTACCTGTG	51317
rs375823098	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46029274	AATACTTGTTGAATT[C/T]TTCCTCACATAATAG	51317
rs375838480	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46012894	TTTACATCTAATTAG[G/T]CTTTGCACTGTCTTG	51317
rs375840628	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46116414	TTGAACCATGACATC[C/T]GTTACTCTGTCAATA	51317
rs375853627	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46117034	TTACTTTCTCAACTG[A/G]TATGGAAAAAGTTAG	51317
rs375906197	snp	C/T	0.000153988	0.00877328	intron-variant	PHF21A	GRCh38.p7	11:45965264	AGCCCAGCAGCCATA[C/T]GCCTCAACGACAAGG	51317
rs375955278	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46100286	AAAAAAAAAAAATCC[C/G]ATGAGCATGGACTTT	51317
rs375962099	snp	C/T	1.65444e-05	0.00287609	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965449	CAGTCTGCCCATTGA[C/T]GACACGGACGGGGTG	51317
rs375964519	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46005690	AACATTAGGGGAACC[A/G]TCAGCACCAACTACT	51317
rs375969390	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46014164	CCCTTGCTCCCATCC[G/T]TCCCTACTCACTTGT	51317
rs375980932	in-del	-/ATGT/ATGTATGTATGTATGT			intron-variant	PHF21A	GRCh38.p7	11:45987251	CTGTATCATAAATAA[-/ATGT/ATGTATGTATGTATGT]ATGTATGTATGTATG	51317
rs375993601	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45991279	GTACCTTGATTTTTT[-/T]CCATATGGTCTAATG	51317
rs375997507	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45990969	AACATATAATGACAT[A/C]CAGCCACCATTATAC	51317
rs376002458	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46096991	AGTCATCTTAAGACT[C/T]TTCTTTTACCACACT	51317
rs376018191	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46047073	CAAGTAACAAACTTT[C/T]AGAAAATAAATGTAG	51317
rs376023086	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45964067	CCAGGCATGGTGGCT[A/G]ACGCCTGTAATCCCA	51317
rs376036340	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45949216	TCTGCTGAAACTTAG[A/G]AAAAAAACCTAAGGG	51317
rs376039512	snp	A/T	0.000296477	0.0121717	intron-variant	PHF21A	GRCh38.p7	11:45949385	TGAGGGAAGGGCCAG[A/T]TGCTGGCCAGTAATA	51317
rs376077902	snp	C/G			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46117995	AGCTGTAATAAGTAG[C/G]AAGACCCTCAAAATT	51317
rs376080912	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46109636	ACAAATGTACCAATG[C/T]GTATACTGTTAAGAA	51317
rs376095916	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46062810	ACAACCCAGACATAC[G/T]AAGGCATTTACTGAA	51317
rs376122550	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45961642	TGAATTGACGACATG[A/T]TACATAGAAGTCTTT	51317
rs376126142	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46018150	AGCTACTTGGGAGGC[G/T]GAGGCAGGAGAATGG	51317
rs376136660	in-del	-/A	0.216048	0.247684	intron-variant	PHF21A	GRCh38.p7	11:46025188	ATATGTATACAGATT[-/A]AAAAAAAAAAAACAA	51317
rs376141710	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978117	CCAGCCTGGCCAATA[C/T]GGTAAAACCCTGTCT	51317
rs376146693	snp	C/T	0.00914312	0.0669923	intron-variant	PHF21A	GRCh38.p7	11:45939224	AAGAGTTTTATTATG[C/T]TTTGGTAGAGGACAA	51317
rs376160772	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45995400	CCCCTAACAGGAAGG[A/G]ATCATTCTTACACAG	51317
rs376239944	in-del	A/GAG			intron-variant	PHF21A	GRCh38.p7	11:46021074	TTTAAAAAAAAAAAA[A/GAG]AGAGAGACAAGGTCT	51317
rs376246713	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46105651	TGAATGAGTCTAAGC[A/T]ACTTAAAAATCATAA	51317
rs376264118	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46080285	CACCTCAGCCTCCCG[A/T]GTGGCTAGGACCCCA	51317
rs376272526	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46113568	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAACA	51317
rs376282694	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45951954	TGGGACTATAGGCAC[A/G]CGCCACTGCATCCAG	51317
rs376350658	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46073720	TCAGAGCACATTCCT[C/G]TATCATTAAAATACT	51317
rs376355930	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46016179	CACTATAATCTTATG[A/G]GACCACCATCATATA	51317
rs376359420	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45942469	TTTGGCAATACTTCA[A/G]CTGAGAAAAAGTTGG	51317
rs376365191	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45969755	AGGCTACTTAGAAAG[A/G]GCCCATGAGGATTTC	51317
rs376405992	snp	A/G			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46118126	AAGACTGAATAGGAA[A/G]AAGGATGGACCCTTC	51317
rs376463209	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46107524	AAACTGCTACATTCT[-/T]ACCAGGTCCAATTCT	51317
rs376485879	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46064115	ACTCCACAGGAAAGG[A/C]GTTGTTAATTTTTTC	51317
rs376542909	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46111610	TGGCTAAGCAAGTAA[A/G]AAAGGCACTGCCCTG	51317
rs376547964	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46065966	GTTAGGGCGGGCACA[A/T]CCAAGAGATGACAAA	51317
rs376559174	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46014616	AACTAATTTACATTC[C/T]CACCAACAGTATATG	51317
rs376567404	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46065188	GGAGAAAATCTCCAG[C/G]TCCAGGACACAAATC	51317
rs376577759	in-del	-/CAC			intron-variant	PHF21A	GRCh38.p7	11:45948593	ACATGGGGTTCTGTT[-/CAC]TGTGCTATTCATGGA	51317
rs376591323	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952125	TTTTGATGATAGAAT[A/G]AAAAGCTGTCAAAAA	51317
rs376651509	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45955048	ACTGTGGCAACCAGT[-/T]GCTCTGGGGCACAAA	51317
rs376661614	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45957852	CAAAAGGTGAATCTT[C/T]GAAAAGAATAACAAA	51317
rs376664005	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46021660	GATCCTCCTGCCTCA[A/G]CCTCTCAAGTCTCTG	51317
rs376685241	snp	A/C			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932578	TCTCCAGTTCTGACA[A/C]CTTTTTAATAGAAAT	51317
rs376709714	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46060801	ATAGTTTCATTTGCT[A/G]TGCAGAAGCTCTTTA	51317
rs376717186	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46086801	AATTCACATAAACTC[C/T]GGAAATGAACGGCAG	51317
rs376734638	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46009963	ATTTTCATTAAATAA[A/G]TATCCTAATTTGTTC	51317
rs376739810	snp	C/T	1.71278e-05	0.00292637	intron-variant	PHF21A	GRCh38.p7	11:45938127	CTTTGTCCTCCTCGG[C/T]CCCTCCCCTGTTGGA	51317
rs376740465	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45984474	CAAGACAGGTAGTCA[C/T]GGTGATCAATATTGT	51317
rs376744076	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931755	CAGGGCCAGGGTACA[G/T]AGCCTCCACCGCCCT	51317
rs376748069	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985979	TTAAAATTCTCTGCA[C/T]GGATGTTTAACAGAT	51317
rs376758846	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46094664	AAAGTGGGTGGATCA[C/T]GAGATCAGGAGATCG	51317
rs376760054	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46109796	AGACCAGTCTACCCA[A/G]CATGGTGAAACCGTC	51317
rs376784157	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45994873	GCTTTGAATGTCTCC[C/G]TGGTATTTCTCTGTC	51317
rs376784976	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46041660	ATGAAGACCCAGATT[C/T]AAAACAAAGAAAACA	51317
rs376794452	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46012681	GTAAGTAAATCTATA[C/T]CTCTAGTGCTGGCCT	51317
rs376825223	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45961801	GGAGAGGACAAGGAC[-/A]GGGGAGGTGATGTGA	51317
rs376845222	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45991832	TTACCTCTATAGCAC[C/T]GCACAGAGAAAAATG	51317
rs376852559	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46067883	AGGCACAAGTACCAA[A/G]TACCATGAGTACACA	51317
rs376862003	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46031336	TTCTTCCTTTCCATA[C/T]AGCACTGCCAGATTA	51317
rs376869895	snp	C/T	0.00557542	0.0525036	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929394	AGCTGCTCTGTATCC[C/T]CCCCCACCCCCTCAA	51317
rs376876604	snp	A/G	1.65594e-05	0.0028774	intron-variant	PHF21A	GRCh38.p7	11:46076710	AGCAGACATATCTTT[A/G]GAACACAACGTTAAA	51317
rs376878944	in-del	-/TG			intron-variant	PHF21A	GRCh38.p7	11:46008287	CAATTGAAATTTTCC[-/TG]TGTGTGTGTCCTTAT	51317
rs376888297	in-del	-/AGGAA			intron-variant	PHF21A	GRCh38.p7	11:46079851	GAAAGGAAAGGAAAG[-/AGGAA]AGGAAAGGAAAGGAA	51317
rs376930194	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45981940	TCTCTTTTTGTTTTT[-/C]TTTTTTTTTTTTTTT	51317
rs376976172	snp	C/T	0.000153988	0.00877328	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46076812	AGCTGTTTCTTTAAG[C/T]CAGCATTCTGATTGG	51317
rs376981110	snp	C/T	1.64893e-05	0.0028713	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934132	TGGAGAGGTCGATGC[C/T]GTGGATGAGGCGAAT	51317
rs377000937	snp	C/T	5.03799e-05	0.00501871	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45969834	GGAAGAAAGTTTGGA[C/T]GTGGAGTGAGTCTAG	51317
rs377010277	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45941649	ATACAGAACCGGCTC[C/T]TTGCCTAAAAAGAGC	51317
rs377034785	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46018118	AGCCGGGCGTAGTGG[C/T]GGGCGCCTGTAGTCC	51317
rs377098329	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46042454	ACAGGCCAGGGACAC[A/G]TTATAAGACTGGACT	51317
rs377100266	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46076216	GATGTTCTTCTCCTG[C/T]CCTATATAGAATAAG	51317
rs377120635	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46112707	TCTGAAATTAAATAC[C/T]GGCACAGAAAACCTT	51317
rs377133610	snp	C/G	1.71023e-05	0.00292419	intron-variant	PHF21A	GRCh38.p7	11:45934250	ATGACAAGGGCAGTG[C/G]CACTGAGCCGCCTGG	51317
rs377190327	snp	C/T	0.000141161	0.00840002	downstream-variant-500B, stop-gained, synonymous-codon, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928837	CCCCAGAGCCCTGCC[C/T]GAGGCTGAGGCTGGG	51317
rs377198834	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45967332	GAGATAGTGCCACTG[C/T]ACTCCAGCCTGGGTG	51317
rs377208245	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45976367	AATTCTTGAAAATAG[A/G]AACTCTCTGATTTGT	51317
rs377225039	snp	C/T	0.00953873	0.0683987	intron-variant	PHF21A	GRCh38.p7	11:46038374	CTCAAGTGATCCACC[C/T]GCCTCAGCCTCCCAA	51317
rs377235822	snp	A/C/T			intron-variant	PHF21A	GRCh38.p7	11:46037555	CTGAGGCAGGACAAT[A/C/T]GCTTGAATCCGGGAG	51317
rs377250717	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46098898	TGAGAACCCTTTCTA[C/T]TGCACTAACTGTAAC	51317
rs377331573	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45987029	CATCCCAGATTTCTT[A/G]TACCTCTATGGTGGT	51317
rs377335686	snp	A/G	0.000556638	0.0166736	intron-variant, stop-gained, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935237	CGGATGGGCCCACTC[A/G]CTCAGGTGACTAGGA	51317
rs377348550	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45971554	CTACAGAGAAAGGCA[A/G]TCTCTAGTTTTCAAG	51317
rs377350218	snp	A/C	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46115256	ATGGCTGAACCTCAC[A/C]TATAATTTCTAAAAG	51317
rs377350910	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45955957	AACTAGTTTGACTGT[A/T]AACTTGTGAAGGACT	51317
rs377353890	snp	C/T	1.64868e-05	0.00287109	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45950240	TACCAACCCTAGAGA[C/T]ACCATGAAGGCAAGT	51317
rs377364377	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45987286	TATGTATGTATGTAA[C/G]CTGACCCATCAAAGA	51317
rs377373121	snp	A/C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46018025	GGAGGCCGAGGCGGG[A/C/T]GGATCACGAGGTCAG	51317
rs377406433	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45963360	GGGAGGTGGAGGTTG[A/C]AGTGAGCTGAGATCC	51317
rs377421334	snp	C/T			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123043	TTTTGTTTTTAAAGC[C/T]CAGCACTTTTGTAGC	51317
rs377425089	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056462	GTTCTCAAATTAGTA[C/T]GAGCTAATATCACAG	51317
rs377436640	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46030818	CATAGTGTGTGTGTG[C/T]GCGTGTGTGTGCGTG	51317
rs377491821	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46022429	CACTGCACTCCAGCC[C/T]GGGCAACAAAGTGAG	51317
rs377494614	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45975809	ATTGCTTTCTCTACG[C/T]CTTGGTATATGCCAA	51317
rs377546343	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46115405	ATATAAGAATTATAC[A/G]AAAGCCTACAAAATA	51317
rs377599410	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46113445	GAAAAAGCAAAAAAA[-/A]CTTGATGAATAAAAA	51317
rs377627425	snp	C/T	2.39037e-05	0.00345706	intron-variant	PHF21A	GRCh38.p7	11:45965634	AAGAGAGAATAATTA[C/T]TGTATTACTTAAGCT	51317
rs377627620	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46099965	AGTCCAACATATTGA[G/T]CCTTTCTCACCACTG	51317
rs377635061	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46108912	ACGCACTATGCTTGG[C/T]AATGGATATACAAGG	51317
rs377652694	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46000521	AAAGACTCTATAACG[C/T]TTTTCTTTTGAAAAG	51317
rs377655058	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45969332	GAAAGTCCTCTGTAC[A/G]GACCCCTAGCCTAAG	51317
rs377658544	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46080550	CTATAAACAATAGGT[G/T]CCTTACAAAAAAGGT	51317
rs377664648	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46005245	CACCTGACCTCAAGT[G/T]ATAGATCATAGTCAA	51317
rs377667851	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45980479	AAAGTACTCAGAACT[A/G]TGATTGGCACATTGT	51317
rs377669384	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45945398	GCTCAACAGTTTCTG[A/C]TCAACAGTTGCTCTA	51317
rs377700825	snp	A/C/T	8.44959e-05	0.00649929	synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934031	GGAGGGGGAAGGGGC[A/C/T]GGCGTGGAGGTGGCG	51317
rs377702246	snp	A/G	0.000347687	0.0131804	intron-variant	PHF21A	GRCh38.p7	11:45953491	AATAAACCATACACC[A/G]TAGACTGAGACCTGC	51317
rs377734291	in-del	-/T/TTTCTTTTTTTTTTT			intron-variant	PHF21A	GRCh38.p7	11:45971890	GTGTCTTTTTCTTTC[-/T/TTTCTTTTTTTTTTT]TTTTTTTTTTTTTTT	51317
rs377755781	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46096186	TCTCTTACCCTCTCC[G/T]GGACATTCCTCTAGC	51317
rs377762575	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46082291	GAAATGCAACAAAGC[A/G]TGGCTTTTGTCCCAC	51317
rs377765542	snp	C/T	0.00993419	0.0697739	intron-variant	PHF21A	GRCh38.p7	11:46105027	TTAGTACTTACTATG[C/T]GTCAGGCACTTCTAC	51317
rs386373756	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45989491	ACCCCATCTCTACTA[-/AA]AAAAAAAAAAAAAAA	51317
rs386373757	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45989509	AAAAAAAAAAAAAAA[-/AA]ATACAAAAAATTAGC	51317
rs386373758	in-del	-/TT			intron-variant	PHF21A	GRCh38.p7	11:46092760	AGATGTGTCTCACCT[-/TT]TTTTTTTTTTTTTTT	51317
rs386373759	in-del	-/TT			intron-variant	PHF21A	GRCh38.p7	11:46092774	TTTTTTTTTTTTTTT[-/TT]TGAAACAATGTCTTA	51317
rs386753193	multinucleotide-polymorphism	AC/GA			intron-variant	PHF21A	GRCh38.p7	11:45976634	ATCACTTGAGCTCCG[AC/GA]GTTTGAGACCAGCCT	51317
rs386753194	multinucleotide-polymorphism	AAG/GAA			intron-variant	PHF21A	GRCh38.p7	11:45998612	CCACCTCCCAGGTTC[AAG/GAA]TGATTCTCCTGCCTC	51317
rs386753195	in-del	AGACTCTATAAC/GCTTTAAAGACTCTATAAT			intron-variant	PHF21A	GRCh38.p7	11:46000508	TTTAAACAGCTTTAA[lengthTooLong]GTTTTTCTTTTGAAA	51317
rs386753196	in-del	ACCAACCTTCTA/CTCT			intron-variant	PHF21A	GRCh38.p7	11:46035420	TCTAGTATGTTTTGA[ACCAACCTTCTA/CTCT]GTTGGTTACTTCATT	51317
rs386753197	multinucleotide-polymorphism	AT/TA			intron-variant	PHF21A	GRCh38.p7	11:46039197	CAAATCTTACTGAGA[AT/TA]ACTAATGAAACGTTT	51317
rs386753198	multinucleotide-polymorphism	AC/CT			intron-variant	PHF21A	GRCh38.p7	11:46089961	CCTGGACCCCTCCCT[AC/CT]CATCATCAGTGCTCA	51317
rs386753199	multinucleotide-polymorphism	AAA/GAG			intron-variant	PHF21A	GRCh38.p7	11:46115178	TGAAAGGGAGAAGTG[AAA/GAG]GAGTATTCAAATTGC	51317
rs397705535	in-del	-/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:45974628	TGGCTAATTTTTTTT[-/T]ATTTTTAGTAGAGAC	51317
rs397708802	in-del	-/C	0	0	intron-variant	PHF21A	GRCh38.p7	11:46110571	TTTTCTATATTGGCC[-/C]ATTAACACCAGGGAC	51317
rs397710298	in-del	-/TTA	0	0	intron-variant	PHF21A	GRCh38.p7	11:45978356	AATCCTAAGAGGAAG[-/TTA]TTATTATTACCATCT	51317
rs397718456	in-del	-/CT			intron-variant	PHF21A	GRCh38.p7	11:45962310	ACGGGTTTGGTAACT[-/CT]GTGAACAGGTGTGAA	51317
rs397722590	in-del	-/A	0	0	intron-variant	PHF21A	GRCh38.p7	11:45970594	CAAGTTTTGTTCAGG[-/A]AAAAAAAAAAAATCC	51317
rs397727935	in-del	-/G			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123027	TGGGGGGGTGGGGGG[-/G]TTTTGTTTTTAAAGC	51317
rs397733115	in-del	-/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:46095197	AAATAGAATATTTGC[-/T]TTTTTTTTTGACAAT	51317
rs397737192	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45951824	TTTTTTTTTTTTTTT[-/T]GAGGCGGAGTCTCAC	51317
rs397740160	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45998530	TTCTTTTTTTTTTTT[-/T]AAACAGAGTTTTGCT	51317
rs397742571	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:46114104	CACACACACACACAC[-/AC]GCACACATCCCCACA	51317
rs397766658	in-del	-/A	0	0	intron-variant	PHF21A	GRCh38.p7	11:46067612	CAAAAAAAAAAAAAA[-/A]CTGAATTGAATCATT	51317
rs397783389	in-del	-/AG/AT	0	0	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931275	GAAAAGGTAAGTTAG[-/AG/AT]GTGTTGTGTGGCAAC	51317
rs397793375	in-del	-/G	0	0	intron-variant	PHF21A	GRCh38.p7	11:46089053	TTTTAGGGACAGTTT[-/G]GGGGCACACTGTGTC	51317
rs397799545	in-del	-/TT			intron-variant	PHF21A	GRCh38.p7	11:45966196	TATGTACTGAAGACT[-/TT]CACACTTTTACCTCA	51317
rs397803889	in-del	-/T	0	0	intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119758	TGCTGTTAGGATTTC[-/T]TTTTTTTTTTTTTTC	51317
rs397806172	in-del	-/TT	0	0	intron-variant	PHF21A	GRCh38.p7	11:46092775	TTTTTTTTTTTTTTT[-/TT]GAAACAATGTCTTAC	51317
rs397812175	in-del	-/TT	0	0	intron-variant	PHF21A	GRCh38.p7	11:45943140	ttttttttttttttt[-/TT]gagacagggtcttgt	51317
rs397847961	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46003285	AAAGGCTAACATTCA[-/A]AAAAAAAAAAAAATG	51317
rs397848568	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46003284	TAAAGGCTAACATTC[-/A]AAAAAAAAAAAAAAT	51317
rs397943601	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45950540	TTCAAAAAAAAAAAA[-/A]TCGCAAAAAAAACTC	51317
rs397949998	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46096390	GTAACCATACTCCCT[-/T]CTAATTCCTCTCCTC	51317
rs398015935	in-del	-/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:45957226	TAATCTCTGCACAAG[-/T]TTTATCCATTACTTA	51317
rs398015936	in-del	-/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:45967384	TTTAGCAATAAGGGA[-/T]TTTTTTTTTTTTTTT	51317
rs398015937	in-del	-/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:45987687	CAATGATTCAGGTGC[-/T]TTTTTTTTTTTTTTT	51317
rs398015938	in-del	-/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:46071744	ATAGGGTGTTTCCAG[-/T]TTTTTTTTTTGGCTA	51317
rs398015939	in-del	-/A	0	0	intron-variant	PHF21A	GRCh38.p7	11:46079430	TTAAATTCCTTTCGG[-/A]AGCCACTGTCACCCG	51317
rs398015940	in-del	-/A	0	0	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084697	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	51317
rs398015941	in-del	-/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:46118435	GAATATTCCAGGGGC[-/T]TTTTTTTTTTTTTTT	51317
rs398015942	in-del	-/G	0	0	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122114	TCGGGCCGCGGAGTT[-/G]GGGGGGGCCGCCGCG	51317
rs398045175	in-del	-/T	0.5	0	intron-variant	PHF21A	GRCh38.p7	11:46028104	CAATTTTTTTTTTTT[-/T]GAAGGATGGGCTTGA	51317
rs398075911	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46016983	TGGATTTTTTTTTTT[-/T]TAATTGAGATGGAGT	51317
rs398075912	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46071743	ATAGCCAAAAAAAAA[-/A]ACTGGAAACACCCTA	51317
rs398075913	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46110570	ATTTTCTATATTGGC[-/C]CATTAACACCAGGGA	51317
rs398115351	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46109561	AACACAAAAGCTCAT[-/T]AATTAAAATTTTTCA	51317
rs527252447	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46063425	ATACTGTCTTTGTCA[C/T]GACTACTTAACTCTG	51317
rs527268473	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005204	CTTTTTGAGCACTGA[C/T]GTGATGCCACAACTG	51317
rs527283221	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46038461	ACTATTTATTGAGCA[C/T]CTCCATGTGCTACAT	51317
rs527284087	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085831	TTCTTGTGAATATGA[A/G]TTTTCAATATATTTG	51317
rs527321594	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45976510	ACCACTGCTCTTTGT[A/G]TACCAGAATCTACCA	51317
rs527376324	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46077132	TTTATAGAAAGTATC[A/C]ATTGACAGAAAACCC	51317
rs527389712	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959781	GGAACAGGAGAAAAT[A/T]TTTGCAAATCATGTA	51317
rs527391479	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968500	CTGGAACTACATACA[C/T]GTTCTGTCCTCTGCC	51317
rs527392286	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46009919	TGTTTCCTTGAAACA[C/G]ATAAAGGGGCCGTCA	51317
rs527421761	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46035462	GTACATATTCAGTAC[A/G]CTACATTGTGTTAGC	51317
rs527439912	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984392	GACATTCGCATCACT[G/T]GGTTTCATCAGGGCT	51317
rs527444990	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026935	TGGAGAGACTGTTGA[A/G]TGTTTGGAACACAGA	51317
rs527478871	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933600	TGCTCTCCTCCCTCC[A/G]CCCGTCCCTGCTCCC	51317
rs527485692	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050763	TTAAAATTGAGGAAA[C/T]AGGAACACATCAGCC	51317
rs527494555	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46101477	GTTAGGGAATAGGTA[C/T]GTGGGGTTATATTAT	51317
rs527556563	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46034803	ACCCAGTTTCCCAGG[A/T]TATAGTGATTGGTCT	51317
rs527574048	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45975879	CTCCCCCTGGCCCCC[C/T]GATTGCTACTTAATA	51317
rs527591742	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46033691	GCCATATATGGCTAT[G/T]GAGCACTTAAAATAT	51317
rs527593778	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042801	CACCTTCTTGCTATG[A/T]CCTCACAGCAAGAAG	51317
rs527611410	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972026	AAACATGTTAGCCAA[C/T]GAGTATATAGTAAAT	51317
rs527616005	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46010498	CTGACTCTAATGCCT[A/G]AATTTCTTTCTGCTT	51317
rs527635969	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930227	GAGGTGGCTGGAGAG[A/G]CAGCCGTGCATGCGG	51317
rs527664790	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45948833	AAGGAGAAGAAACAC[A/G]CACACAAAGCAAAAG	51317
rs527705661	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017282	GGCCTACATCTATTA[A/T]TTTTTAACAGGCATA	51317
rs527711617	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46117601	TTTTTCAACACACTA[C/T]ACCCCTTTCCAAAAT	51317
rs527722659	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46066780	ACGTGCTAGCTCTCT[A/T]GAACCTCACTTCTTA	51317
rs527729242	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957622	TACCAAAACTTATGC[A/G]ATGCTGTGAAAGCAG	51317
rs527772809	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46056970	CTTAAAGATAACTGA[C/T]TTTATTTGCTTTAAA	51317
rs527773782	snp	A/C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963077	CAAATTACAAAATAC[A/C/G]TAAGTTTGATTTTGG	51317
rs527785709	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110330	TAAGACCAAGTCTTC[C/T]GACATCATCACAACT	51317
rs527798574	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46118574	TTTATAAACATTAGC[A/G]TAACTGTACACAAAA	51317
rs527802657	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058512	CCTGATAATTATTTG[C/T]CAAATGAATTGAGGT	51317
rs527803898	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940058	TCCACCACCACTAGT[A/G]AAGGAACACATCGTC	51317
rs527803903	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949268	TGATAAGTCAAAAAA[A/G]ATCTACCACTTCACA	51317
rs527814291	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46001256	AAACTGAAAAACCAT[A/C]AAGGTTAAGTCAAAG	51317
rs527835704	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46079953	ACTTCTAAAGACATC[A/G]CTGCCCAAAGTTAAC	51317
rs527853193	snp	A/G	6.71419e-05	0.00579365	intron-variant	PHF21A	GRCh38.p7	11:45965621	AACCTATAGGGGAAA[A/G]AGAGAATAATTATTG	51317
rs527909995	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46107238	CCATAATTTTTAAAA[A/G]TGTAGAGAGTACTGG	51317
rs527920714	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983331	GAAAAAGAAAGAGAG[C/T]TCTGCATTACAGGTC	51317
rs527958707	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46074663	ATGTGCCACTACACC[C/T]GGTTAATTTTTGTAT	51317
rs527990156	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46025606	CTTATAATCTCATTT[A/T]AAAAATTTTCACTTT	51317
rs527994391	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45966539	GCTTGGGTTCAAATC[C/T]TAGTTCTACCACTCA	51317
rs528000468	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45968148	AAGATTCTCTCAACA[C/T]TGGTTATTACCATTA	51317
rs528003172	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933588	GGATCTGAAACCTGC[C/T]CTCCTCCCTCCGCCC	51317
rs528032292	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46062960	TGACAGAAGGATGAG[C/T]GAGACGACCAAGAAC	51317
rs528035916	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024079	AGTTGCAATTGGTTA[C/T]GAAAGCAAGGAAAGG	51317
rs528039828	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46002951	TAAATGAATTCAAAT[A/C]AAATGAATTAATTGG	51317
rs528079895	snp	A/G			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122227	AAGGGGGGGGGGGAA[A/G]GCCGTGAGGGGCAGG	51317
rs528084200	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054035	TTTTTCACAAGCAAC[A/G]TCGTGGCAGTGGAGG	51317
rs528108221	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062330	GTCTCAGAACTTTTA[C/T]TAGCCAGGCATGAGA	51317
rs528111209	snp	A/G	0.0364509	0.129988	intron-variant	PHF21A	GRCh38.p7	11:46114103	CACACACACACACAC[A/G]CGCACACATCCCCAC	51317
rs528116126	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006311	CAAAAAACCATGAGA[A/T]ATCAGTAAATTCTTA	51317
rs528116601	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46072044	TATACTAGGAATAAA[A/C]AAGCAAATAAAACAA	51317
rs528136640	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937140	GCTGCAGGATGAGGA[C/T]AATATTACAAGGGAA	51317
rs528154938	in-del	-/T			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46118056	TCCTGCTGGATAGCA[-/T]TTAGAGATCTTCATG	51317
rs528164393	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45951001	ATTTCTCTCTGAAGA[C/T]CACTCTTAGGGCTCC	51317
rs528171932	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105951	CAATGTATTTAATTA[C/T]ACAAATATAAGTATT	51317
rs528192552	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46054884	CTTTTAACCAGTAAC[A/G]ACTAGGACCAGCAGT	51317
rs528195571	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945700	AGCTGCCTTACATGG[C/T]ATAAAAAGCATTCTA	51317
rs528200336	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45982103	CTGGGACTACAAGAG[C/T]GTGCTACCATGCCCA	51317
rs528208590	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46114684	AAAATTTAAAAAAAA[A/C]ACACACAATTTAGGG	51317
rs528228626	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006868	AAATACAAATCAACA[A/G]GTACTAACAATATGT	51317
rs528230906	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45997830	CATTCTGCAATTTCA[A/T]CCTCCCTCACCAGCA	51317
rs528248030	in-del	-/AAGG	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46072096	AACTAACAATCTAAT[-/AAGG]AAGACAGATATTTAA	51317
rs528254988	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961682	TGGCAGTGGGGTGGA[A/G]AAGAAACATAATTCC	51317
rs528271782	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46020385	CAAGAACCAGGAGCG[A/C]CTGCTCTGACACTGT	51317
rs528306728	in-del	-/TAAA			intron-variant	PHF21A	GRCh38.p7	11:46004760	CTGTCTCCTCAAGAC[-/TAAA]TAAAGGACTCATCAT	51317
rs528325513	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45978827	TTAAATTGTATGCTT[A/G]TTTAAATGCCCTTTT	51317
rs528334982	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078779	TTTGGGGTCTCTTTT[A/C]ATAATATTGGGATGA	51317
rs528338017	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013436	ATAATGGCCCCAAAG[C/T]GAAAGAGTAGTGATG	51317
rs528380918	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45962290	GTCATAGAGAGAACG[C/T]TGGATACGGGTTTGG	51317
rs528384239	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45998894	GTGGTGTGATCTCAG[C/G]TCACTGCGGCCTCTG	51317
rs528466985	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46095971	TACTATACCAAGCTG[A/C]TAGAGGCCCCCAAAC	51317
rs528483705	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995924	ATTATTTTCAGTATA[C/T]GGCTTTTTTTAAAAA	51317
rs528493774	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935509	AACTGCATTTGCCCA[A/C]GTTAATCACGTTAAT	51317
rs528494951	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45986667	TTCCTTCAGAAAAAT[A/G]TTGGGAATCAAATTA	51317
rs528499254	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46079977	AGTTAACAATAACCA[C/T]AGACAGAAGAATATG	51317
rs528570417	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46087766	TATTTTGAAAAAATT[C/T]TTTTCCTGAGATAGG	51317
rs528589889	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978173	GGCATGGTGGCACGC[A/G]CCTGTAGTCCCAGCT	51317
rs528613492	snp	A/G/T	0.000572099	0.0169035	downstream-variant-500B, utr-variant-3-prime, synonymous-codon	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928855	GGCTGAGGCTGGGCC[A/G/T]GCGCTGCCCCTCATC	51317
rs528626238	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46017198	CTGGTCTCAAACTCC[A/C]GACCTCAGGTGATCC	51317
rs528661646	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45951241	ACATCTTCAATTGTA[A/G]AAGACATACTCCTGT	51317
rs528680626	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011457	AGATGGTGCCACTGC[A/G]CTCCAGCCTGAGCGA	51317
rs528711676	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120564	GGGTGGAGGGCAGAG[A/G]GGAGGGGGGGGAGCC	51317
rs528726926	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960745	GAATTCATGGATATC[C/G]CTTCGATGAATCTAA	51317
rs528757165	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943933	ATCAGACAATCCAAA[C/T]GGAGAGGCATTCTAC	51317
rs528791025	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46003992	AAATGCTTCAATATA[C/T]TAAGTTTCAGCTGTA	51317
rs528796372	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122217	CAGCAGTTTGAAGGG[C/G]GGGGGGGAAAGCCGT	51317
rs528817810	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112011	TGGATATTCTAACAG[C/T]GCAAACATTGTAAAC	51317
rs528818371	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943171	TCTGTCACCCAGGCC[A/G]GAGTGCAGTGGCGCA	51317
rs528842875	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111632	ACTGCCCTGCTTCTG[C/T]ATACATTCAAACTAA	51317
rs528845918	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952203	TGTTTATGGCAGTGA[C/T]TCTGTCCAACTAGAA	51317
rs528854865	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122387	ACCCCGCCCCCTTTC[C/T]AAATAACTACCCTTG	51317
rs528869395	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45962129	CTAGAAACTGAGTTC[C/T]GTGAGGGTACGGGCT	51317
rs528907518	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113699	GGCGTGGTGGCGCAC[A/G]CCTGTAGTCCCAGCT	51317
rs528910654	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021066	ATAGATTCTTTAAAA[A/G]AAAAAAAAAGAGAGA	51317
rs528914359	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46012386	TTCAAGTTTCTGTCC[A/G]GGCCTTCTTTGTTTC	51317
rs528926740	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45967778	GACTGAACTTAAAAC[A/G]ACCCTGTGGTGGGTG	51317
rs528931546	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961490	AAAACAGAAATTTGA[A/C]GATAATGCATTGGAT	51317
rs528971357	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006117	GTTATTTTACATTTA[C/T]GATTAAAGAACCAGA	51317
rs528974607	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944146	GCAATCTGAATATGG[A/G]CTGTATATTTTATAT	51317
rs528978600	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45953098	TGGTTGTAACAAAAA[C/T]GCACACTTAACAACT	51317
rs528991243	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123340	AAATTAAGTTTAGTT[C/T]CTCAAGAAAAAGCAA	51317
rs528991673	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45979162	GCTGGGATTACAGGC[A/G]CCTGCTACCAGGCCT	51317
rs528994763	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46062245	TGGAATTATATGCCC[C/T]TCGGTTGTGGGACAT	51317
rs529013494	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005193	AAAATCCAAAACTTT[G/T]TGAGCACTGACGTGA	51317
rs529017042	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46077628	GGAACACATCTTCCT[C/T]GTCTATTAAATTTGG	51317
rs529047492	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087715	TAGAGAAGGGGTCTC[A/T]TATGTTGCCCAGGCT	51317
rs529054999	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036748	TGATTTTACCTTGTA[C/T]ATGGACATCTTACTA	51317
rs529057855	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45968907	CTGCACTCCAGCCTG[G/T]GCGATGGGAGCGAAA	51317
rs529083622	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46095816	TTAATTCACCCTACT[A/G]CAAATTTCAAATGAT	51317
rs529091070	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46086844	AGAACTTAACATTAT[A/T]CATAACAAAGGGCTA	51317
rs529101469	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933146	CCTGGACACACACAT[C/T]CTTCTTCCCTGCCTT	51317
rs529142277	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987457	ACAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCA	51317
rs529146148	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46117510	TGTATTTATAAAGCC[A/G]AGTGCCTAAAAATTG	51317
rs529154526	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019937	TAATCATCATGTCAT[C/T]TCATTTCAAATTGTG	51317
rs529184871	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45969942	AAACCAGAGAGAACA[A/G]TTACTCTTCAATATC	51317
rs529212921	snp	C/T	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:46028092	AATCTCTGGGGACAA[C/T]TTTTTTTTTTTTGAA	51317
rs529224940	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46115277	TTTCTAAAAGCTTTG[C/G]AAGAGTTCACCATAA	51317
rs529238607	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994857	TGTCTAGTCATCACA[C/T]GCTTTGAATGTCTCC	51317
rs529275349	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46088782	AACTTCTCTACATAG[C/T]ATATATCTAGAAGAC	51317
rs529275654	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050979	TAAAGATAAATATAG[C/T]AGTCTCCGAGTTCTC	51317
rs529296895	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46060028	GATTACAGGCGTGAG[C/T]CACTGCACCCAGCCC	51317
rs529311397	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044163	AGATAAATAATAGCA[A/T]CTATTAACACAAGAC	51317
rs529321202	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111879	AATCCTGTAACACTG[A/T]GAACTACAGTGATAG	51317
rs529352106	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035961	TTGCATTTTTGAAGA[C/T]TCACTCTAGCTACAG	51317
rs529377545	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46032197	AATCTCACAAAAAGC[A/G]AAAATATCATTATAT	51317
rs529380846	snp	A/C	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46094869	CGCGCCACTACACTC[A/C]AGCCTGGCGACAGAG	51317
rs529433199	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46048219	GTCTCCAGGGAGGTG[A/C]ATATTCTAAACATTT	51317
rs529434003	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46103103	AATGGGACTGCACCC[C/T]CGTCACATACAGCAC	51317
rs529456148	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46011863	TATGCAACACAACAA[A/C]ACAAAAAGAGCAAAA	51317
rs529482200	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010376	ATACCTCGCAACAAT[C/T]TTGTGAAGATACTTT	51317
rs529493550	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949337	GGTTTTCAGAGGGGA[C/G]GCACTGAACAGCTCA	51317
rs529495781	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45959766	AAAAAGGCAAACTAC[A/G]GAACAGGAGAAAATA	51317
rs529504555	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067618	AAAAAAAAAACTGAA[C/T]TGAATCATTTAAATG	51317
rs529558339	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120351	CCTCCCCGGCCGAGG[A/G]ACAGCCGAGGGGGGG	51317
rs529564751	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46111289	AGCCTGGCCAACATG[A/G]TGAAACCCCATCTCT	51317
rs529570971	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45951115	TTCTATTCTTTTCTT[C/T]GCTTGCATGTGGTCT	51317
rs529600830	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119692	CTCGATACCAACCCC[A/T]CCCCTACCAGGGCCA	51317
rs529628809	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46061579	AATTAATTCTTTCCC[A/G]TACTTTCCAAAGAAA	51317
rs529635466	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949938	CTTCGCTGTGCTGTT[C/T]AGAAAAAGAAGAGCT	51317
rs529638759	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048385	ATTCTACTGTATGGA[C/T]ATACCACACTTTATT	51317
rs529654304	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930947	AGGGGACAGTGAAGG[A/C]CAGGGAGATTGGGTG	51317
rs529659669	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45991084	TCCTCTTTTTACTGC[C/T]TCCATAGTTCTACCC	51317
rs529663768	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46110108	ATAAATATCTTAAAA[C/T]CCAGCCCCTTATTGC	51317
rs529675599	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46047480	TCTGGATAAAGAAAC[C/T]GAGACAAAAAGGTAA	51317
rs529679882	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46099891	AAAAAGAACCCTGAC[C/T]TTAGGCCTAAAAACT	51317
rs529686309	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939047	ACGTGTTAGCCAGGA[C/T]GGTCTCGATCTCCTG	51317
rs529698499	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45999617	TGTATAATTTAGGAG[A/G]AGCTGAATATTTAAT	51317
rs529714237	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041186	TTTCAAATACAGAAG[C/T]GGAAATAGTCACCTT	51317
rs529720982	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056386	CCAATTATGTCTGGG[C/T]TAAATATGGAGGTGA	51317
rs529733874	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46004378	ACTGTAAAAAACTTG[G/T]ACTTTTGACCAAAGG	51317
rs529743298	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46091130	CCAGTCCCCAAAAGG[A/G]AGAGAGACACCACAA	51317
rs529749434	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040426	TAACTTAGCAATCTA[A/C/T]TTATAAGTAGAAGAG	51317
rs529801313	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100348	GGTCCCATTAGGCAC[C/T]CTATTTTACTTCCAC	51317
rs529801869	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46064473	CAAACCCTGCTGATT[C/T]ACACAAACATTTGCT	51317
rs529842962	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099936	ACAATTTACATTTTT[A/T]AAAAAATCTTTGTAG	51317
rs529848945	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067129	TGCACCTTGATTCAA[A/T]CACATTTGTTTTCAA	51317
rs529904849	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938344	AAAGGTAAGAAAAAG[G/T]ACAAAAAAGGTAAAA	51317
rs529930056	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008224	CTAGACTAATCCATA[A/C]TGTTCAGATGATAAC	51317
rs529939440	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45999107	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC	51317
rs529944822	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45964450	CAGGCAGCATCTGAA[C/G]AGCCTCTCTGAATCA	51317
rs529954369	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073009	GTGGGGAGTGAGAAT[C/G]AGAGTGAATCCTGTT	51317
rs529959282	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46055712	ATCTCTTTATATAAA[C/T]GCCCCAACAATTTAC	51317
rs529960462	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45954317	TTTTTATATTATAGG[C/T]CAAGCTCCAGCTCAC	51317
rs529967221	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107151	CTCATCCTTTTAAAA[A/T]TTTCAAATTTCCTAT	51317
rs529973700	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45947258	CTTGTCTTCTAGGGG[C/T]AAGGTCATTGCTTCT	51317
rs529985493	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46064042	CTCCCCCAATTTCAC[C/T]TGATTATTTTCCTTC	51317
rs530007690	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46021140	TCATAGCTCACTGCA[A/G]CCTTGACCTTCTGAG	51317
rs530028099	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030102	ACGGTCTTTGGACAA[A/G]GAATCAACGCTAAAC	51317
rs530035843	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946529	GCTGGGACAACAGGC[A/G]TGTGCCCAGCTAATT	51317
rs530069145	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45980144	ACATTATTGGTAATA[A/T]GAAACTGATGGTGTA	51317
rs530084750	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080515	GATACTTAGAGGAAT[A/G]ATTATATTAATATAC	51317
rs530119776	snp	C/T	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46065330	ATAAAAAGAGATATT[C/T]AATAAGAAATGGTCC	51317
rs530144173	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963277	ATACAAAAATTAGCC[A/G]GGTGAGATGGCGGGC	51317
rs530182336	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021765	TTTGTTGCCCAGGCT[G/T]GTCTTGAACTCCTGG	51317
rs530187036	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45958684	ACTTTGGGAAGCCAA[A/G]GTCGGGGGATCACTT	51317
rs530199572	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46081210	TGCCAACCATGGGAC[C/T]TCCAAATACACAAGG	51317
rs530212763	in-del	-/T	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46074231	AAATATTGAAAAAAA[-/T]GATTACAGAAAAATG	51317
rs530227984	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45936098	GCCTGGGTGACATGG[A/C/T]GAAACCTGTCTCCAC	51317
rs530235796	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45997566	TCAGATTTCTCCTCT[A/G]CCTAATAACATTTTT	51317
rs530256720	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053901	ATGTGATGATTACAA[C/T]CCCTCCAATGAGATT	51317
rs530261654	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030609	CACCTTGAACACAAA[A/G]TTCAAAAAGATTCTT	51317
rs530264909	snp	C/T	0.0103295	0.0711199	intron-variant	PHF21A	GRCh38.p7	11:46052036	CAAAGGAATAGTCAA[C/T]AGTCAAGGTTGAGAT	51317
rs530286077	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46070175	ACTAGTTATAGGAGG[A/G]ACAGAAACTTCTTTC	51317
rs530288199	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46030829	TGTGTGCGTGTGTGT[A/G]CGTGTGTGTGTGTGT	51317
rs530304787	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46054642	AGATCTTATTACTCT[A/G]CAACTGTTGAGAAAA	51317
rs530308312	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45989080	GGAGGGTGCAAGTTC[C/G]TCACAAGTGCAGCCT	51317
rs530315772	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46045294	TCCCTATGAAAGATC[A/G]TAAGCATTAGCACAC	51317
rs530316773	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097563	TAATCAGAATTGTTC[C/T]GCTCCCCAACTTTTA	51317
rs530340466	in-del	-/A	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45941826	AGGAAGCACTCTGGC[-/A]ATACCAACTGCAATT	51317
rs530356616	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45985450	TTATGGACAAACACA[C/T]AGAAGAGAAACTCAA	51317
rs530391915	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46038475	ACCTCCATGTGCTAC[A/G]TACTATTCTAGGTTC	51317
rs530408755	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46088798	ATATATCTAGAAGAC[A/T]GTAGGCTTTTCTGTT	51317
rs530414073	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46046159	TGTTTTCAAGAGTGT[C/T]CCTGAGCTTATGCAC	51317
rs530423968	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055573	TTGACCTTTCCAATT[C/T]CCTAGAGCAGTCAAT	51317
rs530429194	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037777	ACTTGAACAATACTT[A/G]AAAATTTTAGCAACA	51317
rs530449083	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46097145	TTGCAACAGCCTCCT[A/G]ACTGGCCTCCCCAAT	51317
rs530449496	in-del	-/ATCT	0.433442	0.16985	intron-variant	PHF21A	GRCh38.p7	11:46015899	GTTTTACAGTCATCT[-/ATCT]ATCTATCTATCTATC	51317
rs530451915	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46023812	AATACAAAAATTAGC[C/T]AGGTGTGGTGGCGGG	51317
rs530475936	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930907	CAGGTGGTCACAGGC[A/C]CCCCCCCCTCCCCGC	51317
rs530481323	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45999046	TGGCCAGGCTGGTCT[C/T]AAACTCCTGAGCTCA	51317
rs530488450	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039336	TTCATAGAACTGGTA[A/C]TTTTTTCTTGTCTGC	51317
rs530519706	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45999365	TTGCAGAAATGGAGT[A/G]AGGCAAGTTTCCCTG	51317
rs530522816	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998634	TCTCCTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA	51317
rs530530096	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46007460	CTGGGTTTACAGGTG[C/T]CCACGACCATGTCCA	51317
rs530544626	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46106309	ATCTCCCCTGAGCAC[A/G]AAAGGGTGGGGGGGA	51317
rs530562934	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46064093	GTAAGTTCATTTGTG[C/T]TTCTTGACTCCACAG	51317
rs530565120	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45971980	GAGGTAGTTACCCTG[A/G]AGGCAATGAGTCCCA	51317
rs530579870	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46072143	TACAGATACAGATAT[A/G]CTACTGTAATAGAAA	51317
rs530597403	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45990416	CGAATGCACCACCAC[A/G]CCCGGCTAATTTTTT	51317
rs530623615	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46060445	TTAGCACATACTCAT[A/G]TAAAATTATGTTATA	51317
rs530636195	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46021668	TGCCTCAGCCTCTCA[A/C]GTCTCTGAGACTATA	51317
rs530712436	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46063730	TATAAAAAGGAATAC[C/T]AGAAATTTAAAGAGT	51317
rs530740902	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013906	GTCAGTGAATGAGTG[A/G]TTAGTAAATGTGAAA	51317
rs530753109	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45962424	ATACTGGAAATGAAA[C/T]ATAAATAGAAAACAA	51317
rs530773776	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46080350	TTTTTGTAGAGACAG[C/G]GTCTTGTTATGTTGC	51317
rs530779897	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114781	GCACATGGTTAACAA[C/T]ACTTGGATCTGCAGC	51317
rs530781360	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46071459	CACTTAGGTAAAATG[A/C]CCTATAATAATATGG	51317
rs530794580	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46051211	AAGTATGTGGTTTCT[C/T]ATACTAGATCTAATC	51317
rs530806880	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45988463	CACTTGTATATAACT[A/G]AACACTGGCATTTTT	51317
rs530869620	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021260	GAGATGGGGGTCTCA[A/C]TCTGTTGCCCAGGCT	51317
rs530869714	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029878	AAGGCATAGAAGAAG[A/G]TAAGAATGTGAATCC	51317
rs530883971	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930094	ATTCAGCCCTTTAGA[C/T]AAATAAGAAGGACCA	51317
rs530896262	snp	A/T			downstream-variant-500B, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929086	TTTCATAATTAAAGT[A/T]TTAAAACATCTTTTT	51317
rs530898418	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46088582	CACTGTGTGACTACT[C/G]TCATCCCCAGGGTTC	51317
rs530898556	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45971405	ATTAGGACACTAAAT[A/C]TAAACTAAATAATAA	51317
rs530917661	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929578	CCGTCCCATCCCGCC[C/T]GACTGCAGCTCACCC	51317
rs530953556	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46029177	TCTCATAATCTTTGG[C/T]CAATTTTTTTGCATT	51317
rs530954150	in-del	-/ACAAACTA			intron-variant	PHF21A	GRCh38.p7	11:46049190	AACAGCTTTTTACAC[-/ACAAACTA]ACAAACTAATGTTGT	51317
rs530993650	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943959	TCTACAGAAGAACTG[G/T]CTATCTTTTTAAAAA	51317
rs531011670	snp	A/G	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46079545	GCCCCACACAAAACC[A/G]GCCTGTTCATACACA	51317
rs531018859	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45982746	GCATCAGCAGCCAGA[A/G]AAAGGAACCCTAAGA	51317
rs531034037	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45935874	CAACCCAGTGCAGAG[A/G]ATCTGCCCACCTGGA	51317
rs531049216	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952085	GGTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	51317
rs531077760	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045248	CTTCACTATGTACTG[C/T]CCTGGTCTACCATGT	51317
rs531084545	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987755	AATTTGTAAATTAAG[C/T]TCCAATAGAGCAAAA	51317
rs531108834	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45997286	GCTGTATGTTTTTAT[A/G]ACACTTATCACTAGT	51317
rs531124993	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053116	GATTACATTTTCAAT[G/T]CAAAATTTGTAATTA	51317
rs531143684	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46020634	TTATGAAATTTCTCA[A/G]ATATGAACATGACCC	51317
rs531163745	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46061449	AGGCTTGTATTATTA[C/T]ATAAATAACATTAAT	51317
rs531177421	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943242	ATCCTCCCACCTCAG[A/C]CTTGCAAGCAGCTGT	51317
rs531180955	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45935949	TGGGTCTGGCTTTAC[A/G]TAAATGAGATACCAC	51317
rs531184823	snp	A/C	0.000186431	0.009653	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928897	CAGACACCAGGGCAA[A/C]CTGCCCTCCGCCATC	51317
rs531200255	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036939	TAGTCTTGAACTCCT[A/G]GCCTCAGGCAATCCT	51317
rs531238239	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044334	TCATGCAAGGTAAAA[G/T]AAGTAATTAGAAATT	51317
rs531241045	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053616	TTAATCAGTGTTTCA[C/T]ACAGGCTGAACATTA	51317
rs531241855	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984304	CCAGAACTGCTAGTA[A/C]CGCCCACTTCAATCC	51317
rs531249659	snp	C/T	0.00026775	0.0115673	intron-variant	PHF21A	GRCh38.p7	11:45935569	CCACACGTACTGTTA[C/T]GTATATTGGAAAGGC	51317
rs531257557	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017593	GGGGGAAAAAAAAAA[A/C]ACACCTCCCTCATCT	51317
rs531258973	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026031	ATGTCCTTTAAGTAA[A/G]AGAGAGTCTCAGATC	51317
rs531309182	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45975622	TTTGCATTATGCCAT[C/T]AAAAATTAGAGGGCT	51317
rs531339430	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46070933	TGGGGAAAATCACTT[A/T]TTATCAATATATGCT	51317
rs531344503	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025316	AAACTTACTATGTCC[A/C]TTTCACACAATATGA	51317
rs531412619	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46075672	CGCATAAGAATAGGA[A/G]GGAAGAATATAAAGC	51317
rs531413045	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085579	TTCTTTTCTTCTTTG[C/T]ACCTATAAAGCTTGT	51317
rs531445088	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45962003	GACAGGGGAAGGACA[C/T]GTGAGACCACTGCTG	51317
rs531470811	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032456	TCCTTTTCTTAACAA[G/T]TGCACTCACAAATAC	51317
rs531477737	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46106451	CTGATAAGTTAACGG[A/C]ATCTGTTCCTTTCAG	51317
rs531480289	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45992846	AAAACAGCTTAAAGT[A/G]CCTTACATATAATTT	51317
rs531493514	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45967442	CCATGATTTGGGCTT[-/C]CCTAAGTGGGGTGAC	51317
rs531512662	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940000	TGCACAAGAAGCAAT[A/G]ATAGAGAGGAATGTG	51317
rs531524195	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940668	ATTATTAAAATCAGG[C/T]TGAGGGCTACTCTTT	51317
rs531535576	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46000961	AATAAATAAATTTAT[A/C]TGTCACTTTTTCATT	51317
rs531536679	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100681	AACTTTCACTGACTA[C/T]GCTTCCCCATGCATT	51317
rs531558125	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074465	TCTTTTGGCGGGAGG[C/G]GGGAAGGCATATAGC	51317
rs531559358	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46065480	ATGAATATGGGTCCT[A/G]ATAGTGTTGCTGAGC	51317
rs531574630	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057454	GGCTTAATTTTCCCA[A/G]TGAACCCAGGCTGGT	51317
rs531576161	snp	C/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45948764	CTCAGAGAACAACAA[C/G]AAAACTATTTTCAAA	51317
rs531624612	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101360	TTCCTTTGAGTATAC[C/T]AATGTATCTAACTGT	51317
rs531627480	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46082313	TTGTCCCACTATTTC[A/G]TCAAATGTATGTTCT	51317
rs531674788	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46026392	CTGACAATGAATAGG[A/G]CTTAGAATATCATTC	51317
rs531688781	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46117492	TTAAGTACATCAACC[A/G]TATGTATTTATAAAG	51317
rs531694581	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957273	CTTGAACAACACTAT[A/G]CACCAATTAGACCTG	51317
rs531701989	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46000045	TCTAGGGGAGATTCT[A/C]ATTTTTCGATTGACT	51317
rs531709011	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45961251	CTCTGCACAAACCTA[A/G]AATGAAGTTAATCAA	51317
rs531738445	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46008552	AAGAGTCTGCTTTGA[C/T]TGGCTGTCAAATTTA	51317
rs531752903	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46083231	CGTGCATAGGGCCAA[C/T]TCTGCAGCGGAACAA	51317
rs531754958	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46081610	GGGGTAGGACAGGAC[A/G]AGCTGGCCAACTTAC	51317
rs531756268	snp	C/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46091073	AGGTAGTAAATGCAA[C/G]GATTAACTAGTTCAA	51317
rs531758057	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45974936	GCATGGCAAATACTG[A/C]CAATAGCAAAATCCT	51317
rs531787324	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973046	TCACACCATTGCACT[C/G]CAGCCTGGGCGACAA	51317
rs531829240	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46109216	TGTTACCTATGTGAT[C/T]CGAGGGAAACCTCTA	51317
rs531847142	snp	A/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45981511	CATAAAGCATATAAT[A/T]ACTATTTGGGGCCAT	51317
rs531877636	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46027732	CCCATATGGAAAAGC[C/T]ACTGTCCCAGGAATC	51317
rs531886764	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45979011	TGAATAGTGCAAATA[C/T]AGCACTCTTCTTTTT	51317
rs531892898	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45964624	TCTTTCTCATCACTA[C/G]TCGTTTTTCAAATAG	51317
rs531908194	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982397	GTAAATATTTTTTTT[A/T]AAATGATGCAGAGTT	51317
rs531937697	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099897	AACCCTGACTTTAGG[C/T]CTAAAAACTAAAAAT	51317
rs532027891	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46065098	ACTTTCTTGAATATC[C/T]ATTCTTCTCCACCCT	51317
rs532048941	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46033333	GCAGTGGTGCAATCA[C/T]GGCTCACTGCAGCCT	51317
rs532064630	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100126	CCTCAATCACGCTGA[G/T]AAGTAAGTAGTCCTA	51317
rs532070470	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031682	CGCTCCGAGGCAGGT[C/G]AAATCAAAAAGGTTT	51317
rs532082144	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022870	TCACTGCAACCTCCA[C/T]CTCCTGAGTAGCTGG	51317
rs532085244	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983419	CCACTCAGAAATGAA[A/T]TGTCCCTTACTCCTT	51317
rs532090196	snp	G/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46084058	GACTCTTGGACAAAA[G/T]TGTCTTAAAGATTAT	51317
rs532104149	snp	A/C/T			intron-variant	PHF21A	GRCh38.p7	11:46043913	CAGTAAAAGATGGAT[A/C/T]GCAGCAACTGCTTTA	51317
rs532111422	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46068147	AGGTATCAGTGCTAA[C/T]GAGCTTGAATGCCTT	51317
rs532113922	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46041309	AAAGATAAGTCATTA[A/C]CAAATGAGATCTTAT	51317
rs532114653	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091848	ACACACCCACTGGGC[C/T]TGGCTGGGAATCTGA	51317
rs532117465	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46045782	CTGTGAGTTTCTTAA[C/T]CCCTTTCTGCTCCAA	51317
rs532133035	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932436	CTTTTCTGAGGAGAG[A/T]GAAGGGTGGGGAGCT	51317
rs532140175	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45999387	GTTTCCCTGCTAGTG[A/G]TTGATTATAGGTCTC	51317
rs532142078	in-del	-/C	0.0100141	0.0700482	intron-variant	PHF21A	GRCh38.p7	11:46034222	ATATTAGTGCCCCCA[-/C]CCCCCCCTTGCATAC	51317
rs532148199	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46001300	CAGGGGGGCTGGAAA[C/T]GGGGCTCTAAGATGT	51317
rs532148647	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46103521	TCTCCTCAGAAATGA[A/G]ATACAATGTTTTAGG	51317
rs532178897	in-del	-/TA	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46054273	GTAACCCTTGAAAAT[-/TA]TATCACATAAAGTTT	51317
rs532182262	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963485	CTAAACTGTTAATAG[C/T]AATTAACTCCTGGGG	51317
rs532234251	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974803	TTAGCTAGTTAACAG[G/T]GTCTAAGTATGATCA	51317
rs532271903	snp	A/G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46000875	CAGTGAGCCAAGATC[A/G/T]CACCATTGCACTCCA	51317
rs532272494	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46106554	CAAAGTTTGGTCTTC[A/G]AGATATGATGATTTC	51317
rs532290289	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46117408	ATGCAGTTACTGTTA[C/T]ATCAACAATGACCTA	51317
rs532310616	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048622	TAAAAATACAAAAAT[C/T]AGCCGGGCATGGTGG	51317
rs532311990	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45947576	TGCTCTCTTGTTTAC[C/T]CACAAAAGGCATATC	51317
rs532314776	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45941177	GATCTTGGCTTACTG[C/T]AGCCTCGACCTCCCA	51317
rs532319976	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46031985	GTTCTCTTCCACACT[A/G]ACATGAAAACCACAG	51317
rs532336930	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107994	ACTAATTCCTATGTA[C/G]GGTATCTTTACGCTG	51317
rs532341235	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45964606	TTTTCTTTGCCAAAT[C/T]CTTCTTTCTCATCAC	51317
rs532360231	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46073090	TCCCAGCACTTTGGG[A/G]GGCCGAGGTGGGAGG	51317
rs532399102	snp	A/G	0.00676609	0.0577691	intron-variant	PHF21A	GRCh38.p7	11:45972981	TACTCGGGAGGCTGA[A/G]GCAGGGGAATCACTT	51317
rs532399409	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931707	CTCTGGCCATTCCCA[A/G]GGCCTGGAGTGGGCT	51317
rs532404297	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049233	GAGAAAGTAATACAG[A/C]ACTGTCAGAGCCAGG	51317
rs532433721	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46109048	GCCTCAAAATGATAC[A/G]CTGTAGCTGTGGCCA	51317
rs532444479	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46100016	TCTTTTTATCAGTAC[G/T]TTGAAATGTCAATGA	51317
rs532446895	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46081399	TTCAATGAAAAAAGC[G/T]CTTGATTTTCCTTTT	51317
rs532473580	snp	C/T	5.00113e-05	0.00500031	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965380	GTCTGGTCCCTGGAG[C/T]AGCTATCACAATGCT	51317
rs532496011	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46082562	TGTATAAAGGATGAA[A/T]ATAAAAGCTATTAAT	51317
rs532505310	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955528	TCTTGGAGTCTCTTA[A/C]TTCCATTTCTAAGGC	51317
rs532543065	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098714	GGACTAAAACTCTTG[A/T]CATTAACAACAAAAA	51317
rs532579399	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097663	ACACTAGGGTCCAGA[A/T]AAAGACTCACTGATT	51317
rs532597136	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930323	ACGCTGCCTGTTGGG[C/G]CTGAGCCAAGCAGCA	51317
rs532600324	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015411	TTAGCCATAAATTCT[C/T]TGCCTAGGCCAATTT	51317
rs532653900	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089981	CATCAGTGCTCAGCC[C/T]AATATACAGTTTCTA	51317
rs532684289	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023262	TCCATAAGGCAGGCC[A/G]GGATCTGGCAGAGAG	51317
rs532700460	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021331	CCTTCCAAAGTGCTG[A/G]GATTACAGGGATAAG	51317
rs532711125	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45990161	ATACACATGTATGCA[C/T]CCACTAACACAAACA	51317
rs532734007	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46047123	TAGGGACAAATTAAT[A/G]AGCAATTGGTAGAGT	51317
rs532755529	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078229	ACACAATAGTTAGAC[C/T]TGAGTTCTCAATTTG	51317
rs532781361	in-del	-/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45990714	GTCCCTTGATTTGTT[-/G]TTTTTTTTTTAAAGA	51317
rs532792105	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968786	AATACAAAAATTAGC[C/T]GGGCGTGGTGGCACA	51317
rs532832824	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45981309	GAGAATTGCTTGAAC[C/T]TAGGAGATGGAGGTT	51317
rs532850031	snp	A/G	0.0134861	0.0810011	intron-variant	PHF21A	GRCh38.p7	11:46021071	TTCTTTAAAAAAAAA[A/G]AAAAGAGAGACAAGG	51317
rs532855122	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45937733	TGACCTGCCCGCCTT[A/G]GCCTCCCAAAGTGCT	51317
rs532858778	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122337	AATGCAACATGCAAT[A/C]CCCGGCCGCCGCTCG	51317
rs532862001	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039112	GACAGACAACTCTAA[A/G]GACTTGACTTTTATT	51317
rs532865123	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961312	ATCAAAGGTAGGCAG[A/G]TGCAAATAAATGTCC	51317
rs532878302	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930873	GGCTGGGGTGGGGCA[A/G]TGTCACGAGCGTATG	51317
rs532893124	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45993125	AGTACTCTGATTTTT[C/T]AAAATCATTTAATTT	51317
rs532902947	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46069122	CCTCTCGATCTTCAG[A/C]ACTTTCATACTTGCA	51317
rs532908605	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070306	CATCTAATATTATAT[C/T]GAAAAGATCTGTAAG	51317
rs532917093	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45960529	CTGGTGATTGCCAGC[A/G]GCAGAGGGCAAAAGT	51317
rs532926601	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45975972	CCCTCATACATTAAA[C/T]ATATGTATTTAATAT	51317
rs532930534	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042388	GTATGTGTGATAGTG[C/T]AACTCCGGAAAGTTC	51317
rs532931482	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46094718	AATAATAATTATTTC[A/G]TAGAAGTCTCTACTA	51317
rs532932922	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085964	TCCAAAAGTGCAAAA[A/T]TCCTTTAAATTCACA	51317
rs532956528	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45986224	GACTTTAGACCTTTT[A/G]TTTGCTAGCCTGATT	51317
rs532969305	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46093872	GAATGACTTTCTGGA[A/T]CTGTTTTCATCCAAG	51317
rs532974449	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019026	TTGGTCAAAATAAGG[C/G]AAGAAAAAGAAAGGG	51317
rs533039062	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46086754	TTCGTACTTCATTCT[A/C]CTGACAGTAACATAA	51317
rs533047285	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968099	AAAATGGATACTCCA[A/T]GTAAAGTGCCTAGCA	51317
rs533047646	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45951388	AGCCACTTGAGAACA[C/T]AGAAATGTCATTTAC	51317
rs533074220	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46011540	GAAGTAAGAAGATTG[A/G]CAATTTCTAAGATAC	51317
rs533076554	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45946577	GGACGGGGTTTCATC[A/G]TGTTAGCCAGGATGG	51317
rs533098907	snp	A/G/T	0.00557734	0.0525397	intron-variant	PHF21A	GRCh38.p7	11:45976600	TAATCCCAACACTGT[A/G/T]GGAGACCGAGATGGG	51317
rs533106499	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46006744	TGAACTGTCTTAAAC[A/G]CCTATTAGAATGTGA	51317
rs533119019	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035902	TGGACTTGGTCCTAA[A/G]AGCAAAGAGAAGACA	51317
rs533133683	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940992	TATCTGGTGTATATA[C/G]CCTATAATTTTTGGT	51317
rs533135133	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45936285	CCTTGTCTCAAAAAA[C/T]AAATGAATAATAATA	51317
rs533139408	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46034888	TTCCTCAAGTATTTT[C/T]AACATGCCAGAGAAC	51317
rs533150659	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949755	GTCCTGATTTTTAGA[C/T]TGCTGTATATATAGG	51317
rs533163866	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985238	ACCAATATTCATCAA[C/T]GCTGAGGATGCAGGA	51317
rs533187631	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058772	AAGCAGGCTTATTAC[A/G]TTCTCTTTACAAAAT	51317
rs533216507	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46027113	CAGCAATCTAGCAAC[A/G]AGCCTCCCAGATTAT	51317
rs533259296	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46050831	TGTCCAGCAACTGAG[G/T]ATGTGTGCAGGACTA	51317
rs533264109	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45941746	TTACTATAAACCAGA[C/T]GGTAGGTAAGTTGAA	51317
rs533264340	in-del	-/G	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:46105860	CTGAATATCTTGATA[-/G]GTGTATTTAAAACAA	51317
rs533266082	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933621	CCCTGCTCCCCACCC[A/C]AGAAAACAGAAACAA	51317
rs533289677	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45942395	ATCAACTGTCCCCTA[A/G]CATTTGTGTACCACC	51317
rs533301532	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45979039	TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTGT	51317
rs533303486	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46089425	GAATCAATACAAATG[A/C]CAACATTAAAAAACA	51317
rs533328203	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46038094	GCCTCCCTGTATTGA[C/G]TTTACTTGTATACTC	51317
rs533328383	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957836	ACAGACTCAACAAAA[C/T]CAAAAGGTGAATCTT	51317
rs533333166	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025207	AAAAAAAAACAACTT[G/T]TCTCCATCTCCCAAC	51317
rs533376356	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016726	ACATGGGGAGACTAG[G/T]TCTTGCTGATTTTAT	51317
rs533389180	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001855	GGTCTTTGGTTTCTA[C/T]GACAACCCAGATGGG	51317
rs533395868	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119582	CTTAGAAATCACTCT[A/C]GGCACATCTGCACCC	51317
rs533401721	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949312	ACAATCAGGGTGCTG[C/T]TCTTCAGCAGGTTTT	51317
rs533410174	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074723	GGCCAGGCTAGTCTC[A/G]AACCCCTGACCTCAG	51317
rs533433118	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46042804	CTTCTTGCTATGTCC[A/T]CACAGCAAGAAGGTG	51317
rs533460052	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102044	TGTATTTTTAGTAGA[G/T]ACAGGGTTTCATCAT	51317
rs533464663	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45993894	AGTGCCTATCTGAGA[C/T]GAATTTCCTAGAAAC	51317
rs533499006	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111121	CAACTATGTGGGGGG[A/G]GAGGCTAGTATTATT	51317
rs533502077	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45992997	GAAAACTGAAAACTA[C/T]CTTGCTGAAGCTATC	51317
rs533519280	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45968315	TGCCTGCTGCTCCTA[C/G]GATAAGGCCCAGGTT	51317
rs533532518	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967090	TGACCCTTTCCTGGC[C/T]GGGCACAGTGGCTCA	51317
rs533535629	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017704	AAAGATTACATAAAT[C/G]AAATGCAAATGATTT	51317
rs533595875	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45975442	GAATTTAAGGGATTA[C/T]TACTATGGGATCTAA	51317
rs533604360	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46002119	TTACATAAGTAAATG[C/G]TTTCATTAAAATTTA	51317
rs533636673	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010294	ATTTTTAAAATGTCA[A/G]CATTTTGTAAATATA	51317
rs533640819	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119807	AGACCAAAGAGAGGA[C/T]GACGAGAAGTGTTGG	51317
rs533660291	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46118654	TTCAGACATTTTTAA[C/T]GACCCCCTAAAATAA	51317
rs533684608	snp	A/G	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:45958387	GAGCAACATGACAAA[A/G]CCTGGTCTCAAAAAA	51317
rs533690260	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010443	ATTTGTCTAAAATTA[C/T]ACAGTTAAGTGGCAA	51317
rs533696453	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974994	CATTGTTGTCTGCCT[A/G]CCAAATATGAAGTAT	51317
rs533728135	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46067795	CACAGTCCTTGCCTG[C/T]GAGGATCTTACAAAT	51317
rs533729128	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017565	TAAGTTACAGTTCAG[A/G]ATTTGCCCTTAAGGG	51317
rs533734334	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45949104	GTTTTATTGTATGTA[C/T]TTGGCTCTCAGAGAC	51317
rs533738865	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46110374	TGGCCTGGGGCATTT[C/T]ATTAAAAAAGAAAAC	51317
rs533753476	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974255	AGATCTTTACCCCTA[C/T]TCTGGTGCTTCTTCT	51317
rs533755426	snp	A/T	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:45983507	GTGAAAAAAAAAAAT[A/T]TTTAAATCAAGATTT	51317
rs533793920	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45965824	CATAGCTTTTGATTC[G/T]AAACCCTGAGCTCCC	51317
rs533813683	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958061	CACATTACCAAAATT[G/T]ACTCAAGATAAAGAA	51317
rs533816475	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025508	TTAATCATGTATAGC[C/T]CTGGACTACAAAAGA	51317
rs533817990	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075753	CATATCTCTTCCACA[C/T]AATTCTCAAAGTTTA	51317
rs533830338	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085046	TTCTCGGAGGTTAAC[A/G]AATGCCAGGGTAGTT	51317
rs533882035	snp	A/C	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46071332	ACCTAACCAAACCTG[A/C]AGCCTGAAAGGCAAG	51317
rs533889802	snp	A/C	0.00795532	0.062565	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119105	TCCCAGAGTGCACAA[A/C]TGCTTTAAAAAAAAA	51317
rs533898058	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46012586	AGATAAAAGTAGCTA[C/T]CTCAAAGGGCTGTGA	51317
rs533941036	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46088122	CTGGGAGGCAGTTTA[C/T]AGCATCAAAAGAATT	51317
rs533955375	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46108375	AAAGCATGAGGTACA[A/C]TCAATCTAAGGCATT	51317
rs533961333	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084402	TATCTGATTCTCTAA[C/T]GCAGGGCAAGAAATT	51317
rs533961871	snp	C/G	0.00953873	0.0683987	intron-variant	PHF21A	GRCh38.p7	11:46035078	ATTCCTGAGGGAATA[C/G]TGTTCACCTATTCCC	51317
rs533979175	snp	A/G	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:45938655	TTAGGCACAATAAGA[A/G]ATTAACAACAGTGAC	51317
rs533979235	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45947982	TGTAGTCCTGCCTAA[A/G]GCAGACAAAGGGTCA	51317
rs533997446	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933082	ATAAATATAGAAAAG[A/G]GATGGAGCTTGTTTT	51317
rs534000702	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46092006	CAGAAACACAAATGC[A/G]TTTGAAGTATAGCTA	51317
rs534007203	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123320	TTTTACTTTCGTGAC[C/T]TGCAAAATTAAGTTT	51317
rs534008414	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45982992	CTCCTAATCACTGCC[C/T]AGCTAAAGTACACTA	51317
rs534011416	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041558	CTTCTTTCTGGGGTA[C/G]TGTGATTTATTAAGT	51317
rs534011454	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032024	GCTGATAATTTAAAA[C/T]ACAGTCAAAGCCCAA	51317
rs534019863	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46107896	AGTTATCAGCATAGC[A/G]TTTGGTAGTGGTTGA	51317
rs534034226	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091557	TACTATCAGACATGA[A/G]GCTAACTAATCCAAT	51317
rs534063393	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074880	AGCTTTTGAACTTTA[C/T]AGCTGTGCTTCCTTC	51317
rs534068853	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017009	GGAGTCTCACTCTGT[C/T]ACCCAGGCTGGAGTG	51317
rs534095031	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46064921	GCAGGCTGCTAGCTA[A/G]GGTGGCAAAGGGAGA	51317
rs534101738	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46024628	ACAATGGTGAAACCC[C/T]ATCTCTACTAAAAAT	51317
rs534130185	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46073201	GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	51317
rs534154048	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048727	GGGAGTCAAGATGGC[A/G]CCACTGCACTCCAGC	51317
rs534185456	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45999435	ATGTACCCAGTGAAA[C/T]AGCACATAGTATATA	51317
rs534207989	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056108	GCTTCTCTGTTTCCT[A/G]TCTTAAAGTAACAAA	51317
rs534296596	snp	G/T	3.35954e-05	0.00409836	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935722	ATTTAAGTAACTTCT[G/T]TTTCTCTTCTTCTTT	51317
rs534315273	snp	A/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084481	TAAAGAACACTTCAA[A/G]TAACTAAGAAATGAA	51317
rs534315576	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044612	TTTTGCTTCTGCAAC[A/G]GTTATCCAAACTCTT	51317
rs534330772	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46087254	ACTATCAAACAAAAT[C/G]CTCAGGAAAAGAAAA	51317
rs534344039	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45996567	TCCTGGAGTTTTTAA[C/T]GCAGTGCCAGGAATG	51317
rs534351955	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46117811	CAGTGCTCTGTACCA[A/C]GGGCCAGAATCCTTA	51317
rs534353737	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053209	CTAGATCACATCTCT[A/C]ATGGATAGCAGAATA	51317
rs534356772	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935097	TCTTTCCCACTTGGA[C/G]AGGCCGGGCTGGGCA	51317
rs534373656	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014990	GTCTCAAAAAAAAAA[A/T]AAAATAAAAATAAAA	51317
rs534374750	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955682	ATATAAATAATACCA[A/G]AAGGATCCAAAAACA	51317
rs534406017	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46068794	TCCATTTGCCAGCAC[C/T]AAAAATACGTTATTA	51317
rs534406339	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45984229	GGAGAAAAAATTAAT[A/C]ACTTATCATCTTTTC	51317
rs534418927	snp	C/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46030156	TCTGGAGAATATCTT[C/G]CTAATACATTAAAAG	51317
rs534432326	snp	A/G	0.00557542	0.0525036	downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929158	GGCGTCAGTGCACAA[A/G]GGAGGTGCTACATCC	51317
rs534438009	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45964843	TGCTTTTTGGAAATT[C/T]TAATTTTTTTTGTTT	51317
rs534444897	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46096495	AGTTGTTAAATCCAA[C/T]AGAAAATAGTCTTCA	51317
rs534445593	in-del	-/A	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46065679	AAATTCAATGGACAC[-/A]AAAGCCTGTCAGTGA	51317
rs534451639	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008630	GTGACTCGGTTTTGT[C/G]TATGAAAACCTGGTG	51317
rs534454946	snp	A/C	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45987863	TGTATCCCACAACCT[A/C]AAGGCAGCACTGCTT	51317
rs534572471	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113154	ACAGGTCCCAGCATG[C/T]AGTGCTCTAATCTGA	51317
rs534623291	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46061780	TTCTTTGATACTGAA[C/T]TCCCTGTTTTCGGAA	51317
rs534674455	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038100	CTGTATTGAGTTTAC[C/T]TGTATACTCCTATTT	51317
rs534682051	snp	C/G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114598	GGCCAGAGATAGCAG[C/G/T]TGCCATGGTTACTAT	51317
rs534683916	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46044021	TTGTGGTTAACAGCT[A/G]TAAATTTGTTTTTAC	51317
rs534691483	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46036115	AGATATCTAAGAAGA[A/C]GACTGGCAGAACATG	51317
rs534710303	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46088125	GGAGGCAGTTTATAG[C/T]ATCAAAAGAATTATT	51317
rs534712528	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988504	TATTTTTAACAAAAG[C/T]ACATTCTTAATATCA	51317
rs534719753	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039893	CTTATCAATCTGTTT[A/C]GCTTTCTGCATCTTC	51317
rs534729627	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46035387	TTGCCAGCATCATAC[C/T]GTTCACTGACTAAAC	51317
rs534751504	in-del	-/TT	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45947568	AAGATGAATGCTCTC[-/TT]GTTTACCCACAAAAG	51317
rs534783979	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46121891	TGTGCTGCGGCACCC[A/G]TTGCCTAGGGAAAAA	51317
rs534833882	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016191	ATGGGACCACCATCA[C/T]ATATGTGGTCTGTTG	51317
rs534836319	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46052102	GGGACTCCAGTTCCC[C/T]GGCCACAAAAGGATG	51317
rs534848999	in-del	-/AAAT	0.0189856	0.0955633	intron-variant	PHF21A	GRCh38.p7	11:46000924	ACCTCCGTCTCAAAA[-/AAAT]AAATAAATAAATAAA	51317
rs534861257	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46051389	ATTCTTGTGACAGCC[A/G]GAATGAAAACCAGAG	51317
rs534875286	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46049839	GCACTGAGAACCATA[A/G]GTTCCTAAAAACAAC	51317
rs534877497	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46005382	CAGACTGTAGAATAT[C/T]TGCACAATATATTAA	51317
rs534878457	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45995486	TTAGATGGTTAAACC[C/T]CTACTCCCGGGTTTA	51317
rs534881989	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042534	TGGTGAAATGTATAG[C/T]ATGTCTCCTAAACAA	51317
rs534921221	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122562	ATGGCATTTACTTTT[C/G]TGCTTTGTGTAGCAG	51317
rs534922362	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952266	TTGCTTGCCCACACT[A/G]GGTCTAGCTCCATCA	51317
rs534928921	snp	A/C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111363	TAATTCCAGCTGCTC[A/C/G]AGAGGCTGAGGCATG	51317
rs534963045	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004459	GGAAGGGGTAGAGGA[A/G]AGAAGGAAGTCCTTG	51317
rs534964073	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46112423	TGCCAAGCACCGTGC[C/T]AGGTACGGTCATAGA	51317
rs534995110	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45974887	TTGACAAAACCCAAA[C/T]TGCATGAGCTAGAAG	51317
rs535033106	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45976708	TTAGCTGGGCATGGT[G/T]GCCTGTGCCTGTAGT	51317
rs535040766	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994196	AAAATGGAATGGACA[C/T]TGGCAACATTTAGAC	51317
rs535059227	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112314	TTGTAAAAAGAGAGG[A/G]AAAAAATGTGAAGCG	51317
rs535087267	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943320	TAGAGACGGGGTTTC[A/G]CTATATTGCCATCAC	51317
rs535103522	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46114146	CTACAAAGAACACTT[A/T]GAAAAACAGTATTCC	51317
rs535112712	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45969181	CTCAGCCTTCCTACC[A/G]AGGAAGTCAACACTC	51317
rs535121753	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004314	TGGTCTGACATCACA[A/G]ATGGTGTTTTCTATA	51317
rs535127072	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018703	CAAAATCCTGATATG[A/G]ACAACACATTTTTTT	51317
rs535128296	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45951567	ACATACACTTTGTGG[C/T]TGCCAACTAACTACA	51317
rs535143798	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46060652	TTCGTGTCCTTTGCC[C/T]ACTTTGTAATGGGAC	51317
rs535149992	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099405	GGATGAGCAAAACTA[A/T]CTAAATAAAAATTAT	51317
rs535170768	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987127	GGCTCATGCCTGTAG[A/T]CCCAGCTACTTGGGA	51317
rs535175022	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46049124	CATTGTTGGGGCATT[C/T]TCCTCCTTTTCTCCC	51317
rs535212111	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46103499	TTTTAAAAAACTCGT[C/T]GGAATTTCTCCTCAG	51317
rs535216896	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934927	GGAGAAAGCAGGTAA[A/G]CAGGACAGTTCAACT	51317
rs535217035	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45941838	GGCAATACCAACTGC[A/C]ATTTCATCATGTGCT	51317
rs535226620	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995257	TTTTGCCACTAATCA[G/T]AGGGGAGAAAGCACT	51317
rs535241326	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45960116	GCTGTGGAAAACAGT[C/T]TGGCAGTTCTTCAAA	51317
rs535241978	in-del	-/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46057107	ACTACAATTGAGAGG[-/T]TTTTTTCCCCAAGTT	51317
rs535244248	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45993374	TAAGACTCTCAGAAC[C/T]GTGCAGGGCTAATTA	51317
rs535246909	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46104197	CTTTTATATCTCTGG[A/G]GTTCTACAATTGTTT	51317
rs535252284	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944925	GAGCACGCCATGCCC[A/G]GCTAATTTTTGTGTT	51317
rs535252538	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050308	AGGCATAGGGACTAA[C/T]ACCACTGGGTCTTGT	51317
rs535253318	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46101731	GCCTCGACCTACCAG[G/T]CTTAATCAATCCACC	51317
rs535273883	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941237	CCAAGTAGCTGGGAC[C/T]ACAAGTGCGTACCAC	51317
rs535274992	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076480	CCCCATCCCCTATAG[A/G]TAAACTATAGAGTTT	51317
rs535298975	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959218	GCACCCCACTACACA[C/T]ACAAAAAAGGTTAAC	51317
rs535302180	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46000788	AGCCAGGTGTGGTGG[C/T]GGGTGCCTGTAATCC	51317
rs535326810	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111567	ATTGTAAGAACTCCT[C/T]GCAAGAGAAAAAGCT	51317
rs535333965	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094373	AACCCGGAAAAGTTA[A/G]GTGATTTCCCCAAAG	51317
rs535340634	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46069239	ATTTCCTGTATTTGA[C/T]GAAAACGAGGAGCTG	51317
rs535369007	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984740	GCTTCTCTCAAAAGA[A/G]ACTCCAAGACCCTGC	51317
rs535373611	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46121270	GGTTGGGGGGAGGAA[C/T]TGGATCCTCCTCCTC	51317
rs535374477	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45950706	TTTCTCAATGACAGA[A/G]ATCAGTATCTTGTGT	51317
rs535392269	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052267	AGAGGCAACCTCTGC[C/T]AGTACAGGACAGCCT	51317
rs535479079	snp	C/G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111116	AATCACAACTATGTG[C/G/T]GGGGGGAGGCTAGTA	51317
rs535482520	snp	A/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45942229	GAATGTTTCAATTTT[A/T]AAAAAAACCTGGCAG	51317
rs535484825	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46051468	AAGAGTTTACTAGGC[C/T]TTCATTTCCAGTGTC	51317
rs535543146	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086102	CTATGGTGAACAAAT[C/T]TGGGTAGTTTTAGCT	51317
rs535546789	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46076076	GATTACCATAAACAT[C/T]TACTTATAGCTCTAT	51317
rs535566316	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043943	AAATTATATACTTAA[G/T]GATTTATATCAAGCA	51317
rs535579594	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085286	TGTCCAGCTTTACAA[C/T]GAAAATCATCTTCTT	51317
rs535625181	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058937	AGCAGAAATGAAGCA[C/G]AAGCAAAGAAAGATG	51317
rs535629813	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018667	ACATGACTTGGCAAA[A/C]GATAATTTGGTAAAC	51317
rs535718673	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46059787	GCTGGAGTGCAGTGG[C/T]TCAATCTCGGCTCAC	51317
rs535730557	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933643	CAGAAACAAACCCAT[C/T]GTGGCTGTGGAGGCT	51317
rs535741318	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120033	GGGGTGAGGGGTGCA[A/G]GCAGACTCTCCGGAA	51317
rs535794801	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46011307	CAATCTGCCCAACAT[A/G]GTAAAACCCTGTCTC	51317
rs535800061	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46002012	TTCTAGAAGTGGTTC[A/G]GAAGGATTTCATGAG	51317
rs535810137	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101013	ACAAGAAGGAAGTGC[A/G]GAACAAGACTTGTGA	51317
rs535841710	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46034225	TTAGTGCCCCCACCC[A/C]CCCCTTGCATACTTT	51317
rs535843117	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039473	CAGGTAAGTACAGGG[C/T]CCACCTTGAAGGAGG	51317
rs535866216	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030373	GATCTTTTATTCTTA[C/T]CAAATGATTTGCCCA	51317
rs535905623	snp	C/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46093136	AATCAGTGATGAAGC[C/G]AGAAAGAAAATTTAG	51317
rs535907396	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46054518	TGGTCTAAGGTGCAG[C/G]CCTGTATGCAGGATT	51317
rs535933592	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930231	TGGCTGGAGAGGCAG[-/C]CGTGCATGCGGAGAC	51317
rs535954987	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46025636	TGACACAATTTCAGG[G/T]TTACAGAAAAGTTGT	51317
rs535972008	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022302	CTACAAAAAAATTTA[A/G]AAATTAGCCAGGTAT	51317
rs536025138	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45972971	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	51317
rs536029043	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45940352	AGGCGCCCACCACCA[C/T]GCCTGACTAACTTTT	51317
rs536033455	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46109711	ATTGGGCCAGGCGTG[A/G]TGGTTTAGGCCTGTA	51317
rs536064642	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001462	CCTAGGAAATAAATA[A/G]CAAGACTAACAATAG	51317
rs536075912	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998187	TTACTCACAGCTAGG[C/T]TTCCATCTGTGTTAT	51317
rs536084167	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46063188	TGAATTCGCCGGGGG[A/G]GCTGGCATGTTTATA	51317
rs536099286	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46101685	TTGCCCAGGCTGGAG[G/T]GCAGTGGCATGGCAC	51317
rs536100060	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054269	GATAGTAACCCTTGA[A/C]AATTATATCACATAA	51317
rs536100768	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949074	CTAATCATCCTAAGG[C/T]CTCAATGCTCAAGGG	51317
rs536137792	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983718	TCACAATCCAGTCTC[A/G]TTCTAGTTCAGTCTT	51317
rs536151071	in-del	-/TATT	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46089791	TATCTTTCTAATCTC[-/TATT]TGTTTTGGAGGGGGT	51317
rs536162690	snp	G/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46038314	TGTATTTTTAGTAGA[G/T]ACGGGGTTTCACCAT	51317
rs536162731	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46046323	CAACAAGGCTAATAT[A/G]CAAGGGAAACCCACT	51317
rs536209573	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972557	CCGAGGCAGGTGGAT[A/C]GTCTGAGGTCAGGAG	51317
rs536209924	snp	C/T	1.6477e-05	0.00287024	intron-variant	PHF21A	GRCh38.p7	11:45948843	AACACACACACAAAG[C/T]AAAAGCAACAGCAGC	51317
rs536213112	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46055994	TACCTTTTATTGAAA[A/G]TCTTGAAATTTAAAA	51317
rs536251520	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45980942	GTGGAGTGAAAAATT[A/C]ATGTCAAAGTTCTTC	51317
rs536271179	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46108970	GTCTTCATTTCCATC[C/T]CATTCCAATGTTTAC	51317
rs536272262	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45980577	TCACAGGTGTAGTCA[C/T]AGTGCATGCACTACA	51317
rs536284187	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45961867	TTCTGTCTAAAACGA[A/G]TCTTCAGCTTCAAAG	51317
rs536305649	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006399	GCACCTAACGAAATA[C/T]TGCAACTTGTTATAG	51317
rs536310819	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114237	GCTATCAGTAACACG[C/T]CCAAACACAAGCTGA	51317
rs536336950	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46081814	GAAAAAAGCCATACT[C/T]ATTCATTTATATATT	51317
rs536337607	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46008720	ATAATAATATATGTT[C/T]TACATATCTCATATA	51317
rs536357861	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46031006	AAATAATGCAGAGCC[A/G]TAAGGAGCTAGAGCC	51317
rs536453825	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45957309	CATAGAAAGAATACT[C/G]CACTCCACAAGAGCA	51317
rs536460644	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46096347	GTCCCCGTCTAGGCT[C/G]ACGTTTATAGCAAAA	51317
rs536467255	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977850	TTCTTCTTCTTTTTT[G/T]TTTTTTGGTATTGAA	51317
rs536471708	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114912	GCTTCTGTGTTTAAG[A/T]TATTTTTCCCCTAGG	51317
rs536472641	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123375	TAAAAATTCTGATTT[C/G]TTAAAAAATAAAATA	51317
rs536487770	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46063217	TAAGAGAAGGAGCTC[C/T]TACTATTCTGTATAC	51317
rs536499035	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945269	TGAGGTTCATTTAAA[C/G]ATTTAGAGCACTAGT	51317
rs536507899	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930570	GAAAAAGGACCCACA[A/G]GCAGCAAGAATGCAG	51317
rs536521033	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46020534	TAGCTCCCACTTTCA[C/T]TTTTCTGCTTCCCTT	51317
rs536531008	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45979573	TTTGCTTCTTAGTAA[C/T]GTTATTTCCTTCTGC	51317
rs536538404	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970484	ACATCAAAATTTAGA[C/T]ATATTTCTCCCAAGC	51317
rs536538529	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085692	ATACAATAAGATTCA[C/T]GATCTTCATATTTCT	51317
rs536549306	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098265	GGTGTAGTAAACACT[G/T]ATTATCTATTACTTG	51317
rs536556034	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028719	GCTGGGATTACAGGC[A/G]CCCGCCACCACGCCC	51317
rs536570626	snp	C/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46088027	CCTCCCAAAGTGTGG[C/G]ATTACAGGTGTGAGC	51317
rs536571635	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937625	AGCTGGGATTACAGG[C/T]GCCTGCCACCATGCC	51317
rs536581849	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988765	CATGGTGGTGGCACA[A/G]TTGTAGTCCCAGCTA	51317
rs536585965	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46106436	TTTTAGTATCAAGTC[C/G]TGATAAGTTAACGGC	51317
rs536607471	in-del	-/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46058790	CTCTTTACAAAATCT[-/G]GAACAAGAACAAGCC	51317
rs536612497	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123069	GTAGCAACTGCCACT[A/T]CGCATTTTCCAGGCA	51317
rs536614949	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45944143	GGAGCAATCTGAATA[C/T]GGACTGTATATTTTA	51317
rs536616591	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46062064	GACATCTGATTCCCA[A/G]TCCCTGTTTGCAACT	51317
rs536617376	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071546	AAATCTTTGACCAGT[C/T]AGGTATAAGTACTGG	51317
rs536651831	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079694	AAGTTCAGTGGGGCA[A/G]TGATGCTCAGTTTTT	51317
rs536666316	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097363	GTCCCATCTCCCTAT[C/T]GCTCAATCCTTTCCA	51317
rs536673336	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46045422	GAGTTGGGAAAGGTA[A/G]AGAAAGAACAGAGAG	51317
rs536677576	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45985635	AAAATAATTGCACTT[C/T]CTTCATTTTGTAAGA	51317
rs536685152	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45971551	TTACTACAGAGAAAG[A/G]CAATCTCTAGTTTTC	51317
rs536691777	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929276	CTGGGACTGGAATGT[C/G]TCCTGCCCACCCTCC	51317
rs536706337	snp	A/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085758	ACCTAAGTTTTCTAA[A/G]AGTCCTTTGAAAACT	51317
rs536708692	in-del	-/G	0.175254	0.238565	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123021	TACAAATGGGGGGGT[-/G]GGGGGGTTTTGTTTT	51317
rs536751309	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953602	TGTTTGTTTCTCATC[C/T]GTTTCTGTGTGAGAT	51317
rs536780313	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088898	GCAGGTCTTTCATTA[A/C]GATTCTAATAACTCG	51317
rs536801793	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46060871	TTTTGCACCTTCATC[A/G]TGAAATCTGTGCCCA	51317
rs536807203	snp	C/T	0.000174932	0.0093507	intron-variant	PHF21A	GRCh38.p7	11:45953660	TAAAAATTCAGAATT[C/T]GTTTTTTATTAAAAG	51317
rs536836589	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037217	GAAAGGCTATGTTTG[C/T]AGTATATTTTGTGAG	51317
rs536851635	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46027663	ACATTCTCCTTATTC[A/C]CCTTCCATCACATGA	51317
rs536866831	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005462	GGTTTCAAGATAATA[A/C]GAAAAGCAAAAACCT	51317
rs536882356	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044464	CCCTTTCCACCCCCA[C/T]TTGGATTTCATATCT	51317
rs536901620	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105233	ACCTCTGTGTTCTAC[C/T]GACACGCTATAAACT	51317
rs536972098	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46054212	ACTCATTTAAAAAAA[A/T]TTTTTTCTAAAAGGA	51317
rs536982768	in-del	-/TCTC	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46038115	TTGTATACTCCTATT[-/TCTC]TCTCTCTCTCTTTTT	51317
rs536989743	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46018979	ACACACATCATGTAA[G/T]AAGCTAAAACTGTGT	51317
rs537024012	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019522	AATTTAGTTAAACAT[A/T]CTCTACCATACCCCT	51317
rs537028199	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028492	TTCCCTCCTGAAACT[A/C]TAAGACTTCCTGATT	51317
rs537030393	snp	C/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46014760	CCGAGGCGGGCGGAT[C/G]ACGAGGTCAGGAGAT	51317
rs537030500	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45977385	AAAGTGATCCACCCA[C/T]CTCGGCCTCCCAAAG	51317
rs537101139	snp	A/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46012726	CACCCACATTTCTAA[A/T]TCTATCTTAATATCC	51317
rs537107289	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045966	ACAGAGATAAAGTAC[C/T]GTATTAAAACTCAAT	51317
rs537146579	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029629	GAAGGCAAAGGTTGC[A/G]GTGAGCCAAGATCGT	51317
rs537152482	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46038601	GGAATTTATTTCTTA[C/T]AGGTATGGAGGCTGA	51317
rs537209602	in-del	-/A	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45986595	GACCTAAAAGTCCAG[-/A]TGGCTTACATTCAAG	51317
rs537211273	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45986919	AATGACAACTGCCAA[A/C]AAGAAAGTACAATAT	51317
rs537220342	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46033433	CCACATCTGGCTAAT[C/T]TTTGTATTTTTGGTA	51317
rs537243094	in-del	-/GGAT	0.00517822	0.0506191	intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46118129	ACTGAATAGGAAAAA[-/GGAT]GGACCCTTCAAAGCT	51317
rs537246471	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45984380	TTAGATTCCCTTGAC[A/G]TTCGCATCACTGGGT	51317
rs537247166	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995084	GCTTAGATGTTGAGA[A/C]TGAGAAGAGACAATT	51317
rs537256096	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45948240	TGGTGAGAGACACTG[A/C]TGCTGCTACTGCTAT	51317
rs537257538	in-del	-/TTTC			intron-variant	PHF21A	GRCh38.p7	11:46022142	ACCATGTACTGTTTG[-/TTTC]TTTCTTTTTTTATTT	51317
rs537264587	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46103189	AACTCAACCCCCAAA[C/T]GCTTGTAGAATCTCT	51317
rs537312682	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46027529	ATGCCTGCACAGGAA[A/G]CACACAAAATACAAT	51317
rs537343768	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977767	TAGCTATCTGATTTA[C/T]AACAGGGATTTTTCT	51317
rs537345815	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46036154	ATTTCGGAGATGAGT[A/G]AAAGGGAAGAATCAA	51317
rs537365406	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044721	TAAAATTCCTTTTAA[A/G]GAAAAAAAAATCTGC	51317
rs537370971	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45996590	CAGGAATGCTACTCT[C/T]CATATGCACAAAGGT	51317
rs537385324	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114126	ATCCCCACACACACA[C/T]GCTTCTACAAAGAAC	51317
rs537388657	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46040441	ATTATAAGTAGAAGA[C/G]AAAATGTCTGAATAG	51317
rs537392326	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104553	ACTCATTAGATAACA[C/T]TTTTATCATCTATAC	51317
rs537394968	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45980306	GCAGGACTCTGGAGC[C/T]ATCCTACTTCAACTC	51317
rs537396146	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46057529	AAAAACTGTACTTTC[C/T]GTTCTCCATGTTTTG	51317
rs537408316	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46065918	GGAGCTACTGGCTCA[C/G]AGAAGAGAAACCACC	51317
rs537412380	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45998659	CTGGGATTACAGGTA[C/T]GCGCCACCATGCCCA	51317
rs537414951	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079051	AAAAGTTAAGTACCA[C/T]CTATATTTAAGTATT	51317
rs537417935	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45962106	CCTCAGTGCCTGCTC[C/G]AAACACACTAGAAAC	51317
rs537419397	in-del	-/A	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46003215	TATGAGAGTGCCACT[-/A]AAAAAAGTCCTAAAA	51317
rs537426066	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024450	AAGCTTCTCTCTGAT[A/G]TGGCCACCTAGTTTA	51317
rs537452221	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45996171	CTGGTCAGAAACCCC[C/T]GGCTTCAAGTCACCC	51317
rs537457752	in-del	-/CTT	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46024320	TCTCTTTCCTCTGTC[-/CTT]CTCTTTTTCTTGTAG	51317
rs537491640	snp	A/T	0.0111196	0.0737302	intron-variant	PHF21A	GRCh38.p7	11:46096314	ACCCTCTTGACTCCA[A/T]ATCCTTCTCTAGTTA	51317
rs537526074	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122651	AAGTATTTTATGCCT[A/G]TTCTACCTCCAAGGA	51317
rs537532191	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961791	TTAGAGCGCTGGAGA[A/G]GACAAGGACAGGGGA	51317
rs537561922	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45951668	GATGAAGCAGTGTGT[A/G]GACTGATATTCAGAT	51317
rs537585290	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46008957	GTGAACTCAACAAAT[C/T]GGTTCACATTTCACT	51317
rs537590550	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016853	CTTAAAAATTAAACA[A/G]ACACGACCTCAACCA	51317
rs537595823	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011895	CTTCTTTAGTGTAAC[A/G]TTAATTTTAAAACAT	51317
rs537601836	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973379	TCTACTTAGGGGTAT[C/T]AAGTTGTTTGCTTCT	51317
rs537608817	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982863	TAAACATGACACCTG[C/T]CAAAAAATAAACTTT	51317
rs537612570	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977011	TCAGGTGGGCTACTG[C/G]ATGGAGAGGTGCTAT	51317
rs537642530	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031221	CAATAATGTCCCTTC[C/T]AACCTCTTTCCATAC	51317
rs537670813	snp	A/G	0.0119091	0.0762411	intron-variant	PHF21A	GRCh38.p7	11:45982172	ATGTTGCCCAGGCTG[A/G]TCTCAAACTCCTGAG	51317
rs537678035	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052131	TGACTGATTCAAGAA[C/T]GGACCTAAAACTTGT	51317
rs537681334	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46040112	CTGTGCCAGATATAA[C/G]AGGGTTACTAGATGT	51317
rs537712171	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023888	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	51317
rs537804396	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46016556	ATTTCTTACATAAAC[C/G]CTTCCCTAATCCCCT	51317
rs537815815	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45956905	CATGATCTAATGATA[C/T]GCTGTAAGAGAGACT	51317
rs537818658	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46060635	CTTTTGAAAAGTGTC[C/T]GTTCGTGTCCTTTGC	51317
rs537826082	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116055	AAATTTAAGATACTA[C/T]ACCTTTTGATAGGCT	51317
rs537841338	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074122	GGTTTTGTCAGATGC[A/C]AAAAAAAAAAAAGTT	51317
rs537895576	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955599	AATCAATTCCTTTCC[A/C]CTAAAAAATTACCCA	51317
rs537898162	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946309	GAAGTTCCTGGACTA[C/T]TGCAATTTGAGATTT	51317
rs537903382	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46108192	ACCAGTTTTTTTAAA[G/T]GTTATTTGAAAACAC	51317
rs537921526	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46066959	CGTATGTCTGTTTTA[C/T]AATTTGCTTTTTTAA	51317
rs537940206	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990823	CCACCCCACATCTCC[A/C]CACTATCAACAAGCT	51317
rs537947352	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45948448	TTTCCTTCCTGGAAA[A/G]TCTGCAGCTCCAAGA	51317
rs537951468	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958015	AACAAACTAGACAAC[A/G]TAGATGCAATGGAAA	51317
rs538018648	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931776	CCACCGCCCTCCCAT[C/T]GGCCAGGGGCACGCA	51317
rs538020051	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46072491	GGGTTCCCTGACATC[A/G]TGGAACCACTCTCAG	51317
rs538021329	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963549	GATTACGGGGAAAAG[C/T]ACCTTCTACAATTTA	51317
rs538033761	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46040665	TGGTAACAAACCCTT[A/G]CTCACAATTCTATCC	51317
rs538034289	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46026704	TGTGGGCTTTTAAAT[A/C]CGTAATTAAAAAACC	51317
rs538051706	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46080725	CAGGCTGGAGTGCAG[C/T]GGCACAATCATAGCT	51317
rs538061157	snp	C/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46100111	GGAGTCTGAAACATG[C/G]CTCAATCACGCTGAT	51317
rs538144826	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031975	ACATCTTTTTGTTCT[C/T]TTCCACACTAACATG	51317
rs538160468	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45954608	CTTCAAACACAAAAG[A/G]TAGCTAGCATACTGG	51317
rs538170060	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091424	AGCCATTAAAAAAAC[A/C]TCTCAAAGTAGATAT	51317
rs538184225	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46067380	TCTGAGGTAAGTGAC[A/G]TAGTAACATTGCAGA	51317
rs538193220	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055886	AATTGAATAGTTTTG[C/T]TTTGCTAATTCAGAA	51317
rs538226483	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46031802	AACACTATACGCAAA[A/G]GCTGGAAGAATCTGT	51317
rs538230770	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45991693	GTCACTAAACAAGGT[C/T]TGTGACCTTTGGTCA	51317
rs538230839	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46029107	TATCTGTCATGATAA[C/G]CTAAACCTTGTGGAA	51317
rs538256102	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007720	TTAGTTACATTAATT[C/T]AAATCAAAAAACGAT	51317
rs538266094	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46081918	CAGAAATATTTTACT[C/G]TGTGTCCCTTTACAA	51317
rs538299756	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931117	AGCCCAGCTGCAGGC[A/G]AGGTCAGAATGTACC	51317
rs538334286	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45959563	CAATTAGGCAAGAAA[A/G]AGAAAAGGCACCCAA	51317
rs538343644	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45955830	AGGTGTGAGGAACGG[A/G]ACCTCCAGCCAACAG	51317
rs538358206	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938526	ACAATAGTCCCCCCT[A/T]ATCCTTGGGGAATAT	51317
rs538366963	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46047741	GTTGTGTAAGCTTAA[A/G]AGAAGTCACTTTTTC	51317
rs538370966	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45956770	ATGAAGAACAAAAAA[C/T]GTAAGATATACAGAA	51317
rs538388140	snp	A/G	0	0	intron-variant	PHF21A	GRCh38.p7	11:46023736	AGAGGTGGGCGGATC[A/G]CCTGAGGTCAGGAGT	51317
rs538394578	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015049	TAGTTATTCTGACTG[A/G]TGTAAAGTGGTATCA	51317
rs538446369	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038800	ATGATAACCCATGAA[C/T]CTGTGGATTGATTAA	51317
rs538463071	in-del	-/TAAG			intron-variant	PHF21A	GRCh38.p7	11:46100574	TATTAAAGGTCCTGT[-/TAAG]TAAGTATACTCCTTG	51317
rs538480563	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45989675	CTGTCTCAAAATAAA[A/T]AAATAAATAAATAAA	51317
rs538486481	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46046483	AGAGCTCGTCATACA[A/G]GGCAAGAGAAAAGCC	51317
rs538497148	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014788	GATCGAGACCATCCC[A/G]GCTAAAACGGTGAAA	51317
rs538499269	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46097148	CAACAGCCTCCTAAC[G/T]GGCCTCCCCAATTCT	51317
rs538516566	in-del	-/AT	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46109679	CACACACGTAAACAC[-/AT]GTCAAGAATTTGTCT	51317
rs538557744	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46038891	TGCTGCCACATTGGG[G/T]ATTAAGTTTCCAACG	51317
rs538588075	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45965003	GCGTTTTCTGTTTAC[C/T]ACCTCATCTGTGCTT	51317
rs538594889	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45980655	GTAGCTGGAACTACA[A/G]GCACACACCACTGGG	51317
rs538601190	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45960191	GGTATATACCCTAAA[A/G]AACTGAAAACAAGTA	51317
rs538633735	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46006697	CAGCTGGTCAAATGT[C/T]TTATTTAAAAAGATA	51317
rs538645269	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46091296	ATTCCAGCTATCTTA[G/T]TTGAGTGTAATTTTT	51317
rs538676450	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963415	ACAAGAGTAAAACTC[G/T]GTGTCAAAAAAAAAA	51317
rs538709033	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998806	ATTACAGGCATGAGC[C/T]ACCACACCCGGCCTT	51317
rs538714588	snp	C/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:46073958	ACTGAGTTTTAGTCA[C/T]GAAGGATGCTCACTA	51317
rs538725735	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45965951	CCAATAGCCTTAACT[C/T]GCATTTGAAATTTCT	51317
rs538799373	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45971702	ATACTTAATTCTTTT[A/G]GTTTTTCTAGTTCTT	51317
rs538800882	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46115103	TGAGATATTTTCACC[A/G]AAGTCTTTTTTATTT	51317
rs538811363	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938391	CACATTCTAGATGCA[A/T]ATAAATGTTTTAGGA	51317
rs538833347	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45961728	GCATAATCTAATAAA[C/T]ATTAAATACCTGACT	51317
rs538847181	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107409	ATACTCTGTAGGACA[C/T]GGTCTGAGCCACTCA	51317
rs538858080	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098446	TCTAAGTCTTCTTAC[A/G]ATATAAACAAAAACT	51317
rs538928138	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039747	CAAACTAAAATTACA[C/G]ATCACTATCAGGATC	51317
rs538929676	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46090509	AGAATGCTGCATATC[A/C]TATCCCCCTCTTGGA	51317
rs538936631	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013634	CCTTAGGTCATTTCA[C/T]TGCTGTGCGAACATC	51317
rs538946850	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071647	CATCCAGTCATCACA[C/T]ATCTAGGAATTTCTC	51317
rs538949684	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931047	GGTTGCATCTCGTAC[C/T]CCATACTAGCTGACT	51317
rs538960701	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990658	CAGCAAAAGTATTGA[C/T]ATGCATGGTCAAAAG	51317
rs538996868	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45945329	CTACTAAGTATTTGA[C/T]AGTTTTTCCGGAACC	51317
rs539004392	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021408	ATTTTAAACTATTAA[A/C]AAGTATACACCATAC	51317
rs539008010	snp	C/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46014181	CCCTACTCACTTGTG[C/G]AGTCCCTAGTGTTTA	51317
rs539017408	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119899	CCCGGCGGGGGCGCG[A/G]GCGGGGGAGGGGCGG	51317
rs539030861	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45950371	GGCGGGTCTCATGAA[C/T]GCACAAGAGCAGGCA	51317
rs539060259	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46002385	TCAGAAATAAACTAA[A/T]TTGTAACTTTACTAC	51317
rs539068934	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46072320	CATGGGATCTAACTG[G/T]AAGTGGTGCATGCAA	51317
rs539080993	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062646	TTAAATATCTAGTGA[C/T]TCTTGGCTATGTTCA	51317
rs539081256	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46115912	TGTCTGTAGGATGAA[A/G]AAGTTAATAACACCC	51317
rs539101029	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112081	CAAAGGCTTGTGGTA[C/T]GGATGCAATGAGTAC	51317
rs539190715	snp	C/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46001624	CTACATTCTTTTCCC[C/G]CATGCTTACATTTTT	51317
rs539199895	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45967362	GATAGAGTGAGACCC[A/T]GTCTTAAAAAAAAAA	51317
rs539205136	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45980625	TCAAGCAATCTTCTC[A/G]CTTCAGCATCCCAAG	51317
rs539214590	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46097010	TTTTACCACACTCCA[C/T]ATCTACTCCGACAGC	51317
rs539215243	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46029556	AGCTGGGCGTGGTAG[C/T]GCATGTCTGTAATCC	51317
rs539236379	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45979170	TACAGGCGCCTGCTA[A/C]CAGGCCTGGCTAATT	51317
rs539239146	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46080297	CCGAGTGGCTAGGAC[C/T]CCAGGTGCACACCAG	51317
rs539263415	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966804	TTGTATTTTTAGTAC[A/G]GACAGGGTTTCACCA	51317
rs539269199	snp	C/T	0.0103295	0.0711199	intron-variant	PHF21A	GRCh38.p7	11:46007199	CATGCAAAGTGATAG[C/T]GAGGTTCTAAGAGAT	51317
rs539291796	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022123	TTTTCTATTATAGAA[C/T]AAAACCATGTACTGT	51317
rs539302016	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46080642	ACGTCAAGTAGTCAG[C/T]CAGCACATTTTGCTA	51317
rs539302269	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45952373	CAGCCTCCTGGGTAG[C/T]TGGGACTACAGACAT	51317
rs539331350	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119250	GACTATTAGCAAAAA[C/T]GCACAACTCCTTCCC	51317
rs539337654	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46076453	ATCACCTATTCTCAC[C/T]AACTGCCTTTACCCC	51317
rs539381647	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46005514	TAATGGGCACCAAAT[G/T]TTCAGACCTTCCTGT	51317
rs539399398	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059677	TCCTTCTGCCTCAGC[A/C]TCCCAAAGTGCTAGG	51317
rs539426359	snp	C/G			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935047	TGGCTCCTTGCCTGG[C/G]AGAAGCCTCTGTCCC	51317
rs539448723	snp	A/G	3.29625e-05	0.00405958	intron-variant	PHF21A	GRCh38.p7	11:45949516	TTCATTAGCAGAGAG[A/G]CATGGAGAACCTAAA	51317
rs539475911	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102389	AAAGGAAAGGGTCTG[C/T]TACTTTGCAACTATC	51317
rs539489714	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46059165	AATAATCAAAATTAC[A/G]TACAAATATTTACGT	51317
rs539491195	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940264	GCAGTGGCGCGATCT[C/T]GGCTCACTGCAACCT	51317
rs539522082	in-del	-/AAC	0.414489	0.188264	intron-variant	PHF21A	GRCh38.p7	11:46088411	TAACTTTCCAATAAC[-/AAC]AACAACAACAACAAC	51317
rs539523687	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45984552	CCTGAAGAAAAATAC[A/G]GAATTTTATAGGTCT	51317
rs539541450	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092921	CCACCATGCCTGGCT[A/G]TTACTTTATTTTTTT	51317
rs539543268	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084458	AAACAATTCTTCAAG[C/T]ATTCCTCTAAAGAAC	51317
rs539552805	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042420	TCACCACTTGAGCTG[A/G]TCTACGCTGAGGTAC	51317
rs539563854	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46051420	CATTTACCATTACCT[C/T]CCACCTCCATTCTCA	51317
rs539564378	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968866	AACCTGGTGGGTGGA[A/G]ATTGCAGTGAGCCTA	51317
rs539569929	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46074487	GCATATAGCATTAGG[A/T]AACTGTTCTAAAATA	51317
rs539578986	snp	A/C	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46092066	GTGCAAATAGCAAAG[A/C]CCCATTTCTGAGAGA	51317
rs539580712	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101585	ATGTTTTTCTCTAAG[C/T]ATAATTAAATAATAG	51317
rs539592180	snp	G/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084902	AGCCAGGATGGTCTT[G/T]ATCTCCTGACCTCGT	51317
rs539592635	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075889	CATAAAAATCAGTTA[G/T]TGAGAACTATTTAGT	51317
rs539594106	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024769	TGTGCCACTGCACTC[C/T]AGCCTGGGTGACCAA	51317
rs539600629	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46041122	TTTTTTAAACATGTA[C/T]AAAAATCCACCTTCT	51317
rs539603389	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057021	AGATGGTTATAGTAA[A/G]TGCCGAAAAAATTAA	51317
rs539638983	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46076509	TTAATTAACACAGTT[A/G]ACGGCAGCCTGCCAC	51317
rs539670752	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010534	CATTGTTTGGGAATA[C/G]TGGTATGAATAACTC	51317
rs539748930	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939468	AATTAAATTCATATG[C/T]GAGTTCTTTCTAAAA	51317
rs539758745	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048776	CTCCATCTCAAAAAA[A/G]AAATAATTTTTTTTT	51317
rs539763720	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017921	AATTTATTATTTTGG[C/T]TAAATTCATTACTCT	51317
rs539767198	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057741	CTATGAAACTGAGAT[C/T]GGGTCTCATGAGAAG	51317
rs539770935	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009498	CATGTAACGATAATA[G/T]CAGCTGCACACATTT	51317
rs539782702	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46028312	TCTCATATTAATTTC[C/T]ATAAAAATAATAATA	51317
rs539786339	in-del	-/A	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46026635	TGAATTAGAAAATGC[-/A]AAAAAAAAATCCTTT	51317
rs539788194	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46108662	TTTTCTACTTTATAC[A/G]TATCTATATTGCTAG	51317
rs539812948	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041676	AAAACAAAGAAAACA[C/T]TTATTTTTAAGACTT	51317
rs539841300	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100876	AGCAAGTTTCTAACC[A/G]CTGTTACCACGTCTA	51317
rs539851442	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46104945	GCTCAGGCTCTTATA[C/T]TAATACTTGTCTCAA	51317
rs539866643	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45992433	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	51317
rs539898000	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45975079	AGCACTTTGGGAGGC[G/T]AAGGTGGGCGGATCA	51317
rs539958722	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46041188	TCAAATACAGAAGCG[A/G]AAATAGTCACCTTTT	51317
rs539986476	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001570	CACTGCTAGCTAACA[A/C]TGAATTTTTGTATAA	51317
rs540000253	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46109937	AGTGAGCTGAGATGG[C/T]CCCCCTGCACTCCAG	51317
rs540006560	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966145	GTTCTCATTATTCCT[A/G]GGAGCTTTTGCCCAT	51317
rs540007981	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46117149	TGAAGAACTTTTATA[C/T]GTATTATCTCATTTG	51317
rs540027269	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46109426	AAACATTTAAAATCT[A/G]TGTCATTTCTCCAAA	51317
rs540035651	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46034221	ATATTAGTGCCCCCA[-/C]CCCCCCCCTTGCATA	51317
rs540037667	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008769	TTTTGTTAGATTTAA[A/G]TAAATAAATGTAAAT	51317
rs540043225	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46106122	TTGCCACATTTTCTG[C/G]GCTCTCTTTTGAATT	51317
rs540048419	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023911	CAGTGAGCCAAGATC[A/G]TGCCATTGCACTCCA	51317
rs540064692	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46083569	CCAAGGATTAGATAC[A/G]TGCATGTGTATGTGT	51317
rs540065645	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46070198	CTTCTTTCCCAAAAG[C/T]TTCAGAATCTTGTAT	51317
rs540070807	snp	C/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46031743	CTGTTAGGTCTAATA[C/G]TGTCTGGAAAAGAAT	51317
rs540111486	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009069	AACCTCCACCCCCTG[C/G]GTTCAAGCGATTCTC	51317
rs540122941	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46105501	ACCAGGAACTGCAAG[A/G]AATGGGCAATTCAGA	51317
rs540125720	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991580	CACACACATGCACGC[A/G]TGCACTTTTTCTCCT	51317
rs540131121	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45999738	ACTTATTTAGTGATG[A/G]CAAAGCACAGAGATG	51317
rs540139370	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056410	GAGGTGATGACAAAA[A/G]GAAAACTTTTACTTT	51317
rs540144155	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46117688	AAGCCCTAAATCATA[C/T]CAACTACTTTTGTTT	51317
rs540147551	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957032	ACTGTTACGAGAGAC[A/G]AAGAACCTCATTATA	51317
rs540162677	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46000208	CGAAGAAACTGCTAC[A/G]CTATTTCCCTCACTA	51317
rs540181107	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049192	ACAGCTTTTTACACA[C/T]AAACTAATGTTGTTC	51317
rs540200435	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45939825	GTCTTTTCCAGAGAG[G/T]CAATGCCTAGCTCAT	51317
rs540201131	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116689	AAAATTTAGGCCGGG[C/T]GTGGTGGCTCACGCC	51317
rs540208628	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46108922	CTTGGCAATGGATAT[A/C]CAAGGATAAACAAAG	51317
rs540217858	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46020753	GTCCTATAAAGCCAT[A/G]ATAGTTATGGTTGAA	51317
rs540221345	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030627	CAAAAAGATTCTTTA[A/C]TCCTAAAACACATAT	51317
rs540236576	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45981181	ACTTGAGGTCAGGAG[C/T]TCAAGACCAGCCTGG	51317
rs540249848	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931188	CTAGCCCCGTCCTCC[A/G]ACCCAAGACTCCTAA	51317
rs540256031	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46099468	CTCAATATAGCACTG[C/T]TGTACTCACTAGGCT	51317
rs540258714	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45948562	TCTGCTTAATGACTC[C/T]CAAATGCTTCCTTTT	51317
rs540260739	in-del	-/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084429	AATTTCCCAAAGAGA[-/T]TTTTTTTCCCTCAAA	51317
rs540267166	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057295	ATAAGTTTTATGGGA[A/G]AGAGTTTCCCATCAG	51317
rs540278493	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46043433	TTCTGGTTAACATAC[A/T]ACCTTCTATATCTAG	51317
rs540287044	snp	A/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46091778	AAGCTGGATGACTTG[A/T]ATTGGCTCAAGCCAT	51317
rs540292689	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089892	GGCTATTATGGTGCC[C/T]TGGGCCAGGCCAGGG	51317
rs540295099	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45983352	ATTACAGGTCAGATC[A/G]TATGAGCTGGGTAAA	51317
rs540297330	in-del	-/GC	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46094871	CGCCACTACACTCCA[-/GC]CTGGCGACAGAGTGA	51317
rs540312951	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46047806	TGGGGATCAAATTAC[A/G]TAAAGCATGTGAAAA	51317
rs540323992	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932301	GGATCTTATTTAGGC[A/G]CCAGCCTTTTGCTCT	51317
rs540332004	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940431	GAACTCCTGACCTCA[C/T]GATCTGCCCACCTCG	51317
rs540350430	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45964460	CTGAACAGCCTCTCT[C/G]AATCATGGTCCATCC	51317
rs540368399	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45972890	CTGCACTCAGCCTGG[G/T]GAGAGAGCGAGTCTC	51317
rs540377535	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45956069	AGAATTCTATATCCT[G/T]CAAAACTATTCTTCA	51317
rs540392949	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022579	CAATCCTCCAGCCTC[A/G]GTCTCCCAAGCAGCT	51317
rs540404215	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46081372	ATTTTTACATTAATG[C/T]TAGCCACAGTCTTCA	51317
rs540431657	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46063752	TTAAAGAGTTATATA[A/T]AATTTTATCAGCTAT	51317
rs540434594	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073451	AGAGCTTGATGTTAA[A/C]AAAATTTTTTAAATC	51317
rs540437150	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937112	CTGAGAGAAGTGTTC[C/T]GCTGCACCACAGGCT	51317
rs540453192	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023241	TAAGCAATGGTTTCT[C/T]AGCCTTCCATAAGGC	51317
rs540454327	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945573	ACCCCATCTGTTTTC[G/T]GAGAACTCATTCACA	51317
rs540454431	snp	A/G	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:45954801	TTTCATATGGCAACA[A/G]TAATTAAATAAGTGA	51317
rs540455695	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45998589	GTGATCTTGGCTCGG[C/T]GCAACCTCCACCTCC	51317
rs540487013	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098651	CTTAGTAAATCACTC[C/T]TTATCCCAAGACAAC	51317
rs540515208	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46066220	GGAGGTAGTGAACTG[A/G]GGAAGGACGAAGGGA	51317
rs540521604	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45947325	CAAAGGAAAAAAAAG[C/G]GCCAGAGAGATACAA	51317
rs540530960	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45989346	TTAATGAATAAAACA[A/G]ATTTGGTTAAAAATT	51317
rs540572865	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46106741	ACCAAGCTATCCTGC[A/G]TTCTATAAACTGCCT	51317
rs540589037	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040242	GAGTTTCATTAAACA[C/T]AATGGTCTCACCTCA	51317
rs540618379	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45989106	AGCCTGCCAAAATAA[A/T]TACTGATTAACTTCA	51317
rs540621033	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46062965	GAAGGATGAGCGAGA[C/T]GACCAAGAACACTTC	51317
rs540626560	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977348	TGCCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC	51317
rs540670897	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930867	GGAGGTGGCTGGGGT[A/G]GGGCAGTGTCACGAG	51317
rs540675703	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039050	ATTACTGGAGCAGAG[C/T]GAGTGGGCTGAATAA	51317
rs540687225	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46094878	ACACTCCAGCCTGGC[A/G]ACAGAGTGAGTCTCC	51317
rs540702875	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45969680	CTTCATAGTACAGAA[A/G]TCAACAGTCAGAATG	51317
rs540735782	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019723	CTCCGGTTAGATTTA[A/T]CTGGTTCCTTTGTTT	51317
rs540751043	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031463	GGAAGGGAAGGTAAT[A/G]GGAGCTGGAGCCTGG	51317
rs540764740	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968708	CCGAGGCAGGTGGAT[C/T]ACCCTGAGGTCAGGA	51317
rs540766692	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977942	CTTAGCTACACCACA[C/T]ACCACCCTCCATGAT	51317
rs540772500	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46111487	TCTCAAATAAATAAA[A/T]AAATAAATAAATAAA	51317
rs540790079	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055312	GGTTTTTTAAAACTC[A/G]TTGGTTTAATAATAG	51317
rs540806451	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46115455	CAAACATACAAAGTA[C/G]AAAACATAAGCTATT	51317
rs540809695	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101961	CTCCTGTGTTCAAGC[A/G]ATTCTCCTGCCTCAG	51317
rs540847253	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45992643	ATCAAAATTTTATCA[C/T]AATGGAAGAGCTGGG	51317
rs540852784	snp	C/G	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:45941668	CCTAAAAAGAGCAGA[C/G]GAAGTCCTACGGAGG	51317
rs540873239	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059816	ACTGCAACTTCTGCC[C/T]CCCAGATTCAAGCAA	51317
rs540880218	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990089	AATTACAAAATCTAA[C/T]TACAAAATCTAATCC	51317
rs540888638	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45978779	TCATTTCCAAATACG[C/T]CCTTTTTGTGTATCT	51317
rs540910271	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46047024	AATTTAAAGTGATTC[A/T]GGAAGTCTATTCAAA	51317
rs540930082	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45934436	GGCTGGGGGGTCCCA[A/G]GTCCCAGAGGCAACA	51317
rs540931449	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938011	AAGGCCATGCGCCTG[C/T]GTGCTGTGTCATAAA	51317
rs540967882	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998962	CTCCCGAATAGCTGG[G/T]ATTACAGGCACCTGC	51317
rs540971251	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102960	ATAACAGGCAGGGGA[C/T]GGAAAGAGACCATCA	51317
rs540972560	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45994633	GCCTCACCAAGAGTG[A/G]TTATGTTTTAGGCTT	51317
rs540997645	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46068276	TCAATAAATATATGT[A/G]GAATAAAACAGATGA	51317
rs541017417	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45994682	GGGGTTTTGCTGTTG[C/T]ATCATTCTGCAACAC	51317
rs541020867	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036300	TGAGTACAGTTCAGG[A/G]CATCCTGAGTCTAAG	51317
rs541021949	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959541	GTACTGGAAGTTTAG[A/G]CCAGAGCAATTAGGC	51317
rs541024631	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46047460	AAATATTCCTGGCTT[C/G]TTCTTCTGGATAAAG	51317
rs541043906	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987352	ATCTGCACAATTTAG[C/G]TGTTTGTTACCATAA	51317
rs541055643	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035886	AGCCACGTTAAGATT[C/T]TGGACTTGGTCCTAA	51317
rs541059768	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46042157	TTTTTAGGGTGCCAG[G/T]CAACTTAATATAATA	51317
rs541073001	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076165	CATACAAAAAATTCC[A/G]AAGAATATTTTCCAG	51317
rs541085825	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46037469	CAACATGGAGAAACC[C/T]CGTCTCTACTAAAAA	51317
rs541110134	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46059206	ACACTGCAGAGCTAG[A/G]CATACAACAGTAAAA	51317
rs541146453	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120078	AGAAGAAGAATAAGC[A/G]GAATTTCCCCAACGC	51317
rs541154505	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949690	CCACGCTGTCCTACA[C/T]GTGGTTCTCTGTTGA	51317
rs541207010	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45993883	GTTACACCGACAGTG[A/C]CTATCTGAGATGAAT	51317
rs541212761	snp	C/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46003356	CTCAGACTCTCTTCG[C/G]TGTTAATACTGTTAC	51317
rs541246968	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45950834	CAAGCTCCAAATCCT[A/G]AGTGTTTCACTTGTC	51317
rs541259082	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041833	TCTGAAAGTACGCCA[A/G]ATGACATTATTACAT	51317
rs541266752	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45959354	TATTTTAAAAATTCC[A/T]GTTATCTATTCATAA	51317
rs541266934	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46050780	GGAACACATCAGCCT[A/G]TGTGGCTCTTGGCAT	51317
rs541277197	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975959	CCATTCGTCCTTGCC[C/T]TCATACATTAAATAT	51317
rs541346341	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46034289	CATAAGAACTCTTTA[C/T]ATGTAAGACTAATAA	51317
rs541360576	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085440	TAATTTAAATTATTT[C/T]GATGGCTAATTTATC	51317
rs541423266	in-del	-/CTTTAGAC	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45986211	CTCTAAAAATTTAGA[-/CTTTAGAC]CTTTTATTTGCTAGC	51317
rs541424449	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933794	ACACACAGAATAAGA[A/G]GGATCAATTGGCAAA	51317
rs541424636	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46094491	TTCTCTTAACCCGCT[A/G]CAGGAGTTACTCTTC	51317
rs541439732	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45966713	CAGCCTCCGCCTCCC[A/G]GGTTCAAGTGATTCT	51317
rs541504699	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977187	CTCTGTCGCCCAGCA[C/T]GGAGTGCAGTACGAT	51317
rs541507931	snp	A/G	5.42706e-05	0.00520888	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933936	GTTCTCCTTGCCGCC[A/G]GGATCCCGTGGCTTC	51317
rs541512032	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011381	GTAATCCCAGGTACT[C/T]AGGAGGCTGAGGCAG	51317
rs541547146	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010638	TCAACAATCACAAAA[C/T]AAAACAATCTTGGCT	51317
rs541557747	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119473	ACAAAGAATATTTCA[A/T]CATATGACCGGAATA	51317
rs541595675	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094537	AATAAACACTAGCGA[A/G]ATATTTTTGGAAAAG	51317
rs541610956	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110234	GGCCCTTATTATTAT[C/T]CCCATTTTACCACTG	51317
rs541655080	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45939472	AAATTCATATGCGAG[C/T]TCTTTCTAAAATGAA	51317
rs541658100	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949255	TGACTAATAAAAATG[A/G]TAAGTCAAAAAAAAT	51317
rs541664927	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092238	CCTATAACAGAAGAA[C/T]GGGAAAATGGAATTA	51317
rs541673040	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46009175	GACAGGGTTTCACCA[C/T]GATAGCCAGGCTGAT	51317
rs541683281	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101919	GCTGGAAGCAGTGGC[A/G]CAATCTCGGCTCACT	51317
rs541687895	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966979	AACGCTTTCCCCTTA[C/T]GCATGAAGCTTGACC	51317
rs541709475	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46041994	TTTAAAATCCTGTAT[A/G]TCTGTTTAAGTGTTA	51317
rs541710594	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075404	GACTCATTCATTGGC[A/G]TCTTGTCAAACTAAC	51317
rs541714597	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025076	GTGTTCTAGAAACTT[A/T]ATGAAAATAAACACA	51317
rs541741361	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084790	GTTCACGCCATTCTC[C/T]TGCCTCAGCCTCCAG	51317
rs541760977	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45961198	TTGCTGGAATTTGCA[A/G]CTCCTGTTCTTTTTG	51317
rs541767115	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45992847	AAACAGCTTAAAGTA[C/T]CTTACATATAATTTA	51317
rs541771186	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111075	CAGGCGTGAGCCACC[A/G]CGCCTGGCCATATTA	51317
rs541779585	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957375	CTCCAGGACAGATTA[C/T]ATGTTAGGCCACAAA	51317
rs541782564	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46093160	AATTTAGGTTTTGGG[A/G]TCCCAATCCAATATT	51317
rs541784851	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45975347	TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT	51317
rs541794950	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45936072	CACTTGAGCCCAGGA[C/G]TTTGAGACCAGCCTG	51317
rs541805152	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46043428	ATCCTTTCTGGTTAA[C/T]ATACTACCTTCTATA	51317
rs541805360	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46002526	AGCACTATTTGGGGG[A/G]AAAAAAAAGGAATTC	51317
rs541817877	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45966868	GGGATCCACCCGCCT[G/T]GGCCTCCCAGAGTGC	51317
rs541834919	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084566	GCTCAGCACTGTGTT[A/C]ATCACTACATACTGA	51317
rs541838731	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074523	ATTTTATTTTTTTGA[C/G]ATGGAGTCTTGCTCT	51317
rs541846064	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46077853	GTTTACCACATTAAA[C/T]AGGAAAGGACCTGTT	51317
rs541872509	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46073245	AAGTGGGAGAATGGC[A/G]TGAACCCAGGAGGCG	51317
rs541888343	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967921	ACTCTTAATAGTTCA[G/T]ATTCTATTCTATTCA	51317
rs541893128	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46042781	TCCCCTTCTGCCATA[C/G]ATAGCACCTTCTTGC	51317
rs541929164	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46026052	GTCTCAGATCATGCC[A/G]AGTTATCTAAATATA	51317
rs541943558	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085677	CTACTCCTTAAACCA[A/G]TACAATAAGATTCAT	51317
rs541947954	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46107000	ACACCTTTTACCAAC[C/T]GTCCTCCAGCTGTCC	51317
rs541949125	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46075119	TGCCACTTGATGAAA[C/T]GTCTTAACATAGATA	51317
rs541982365	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940686	AGGGCTACTCTTTTC[C/T]TCTAGAGGGTCAGCC	51317
rs541988717	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001717	GTATGATAGGCCATG[A/G]GAGAATAAAACCAAT	51317
rs542028080	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010570	TAAATTATATTTGGC[A/G]CCGGAGTATGCTTTT	51317
rs542058230	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46005393	ATATTTGCACAATAT[A/G]TTAACGCCTTGTATA	51317
rs542063746	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931476	CCCTCAGCCAATCAA[A/G]CAGCCAGGGCCTAAC	51317
rs542069974	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46083921	TTCTTTTTTGTTAAC[A/G]CCTTTGGTATATGAA	51317
rs542101874	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46077413	AAAAAAAGAATACTA[G/T]TTTAGATGAGATACA	51317
rs542103822	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939701	CAGGTAAGTCTGCTG[A/G]AGCCTCTGAACAGAA	51317
rs542106044	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040416	AATTCCAAAATAACT[C/T]AGCAATCTAATTATA	51317
rs542110249	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092132	ATTTGAATAACTATC[A/C]AGCTAGCATCAGGAT	51317
rs542171328	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45953130	CAATTGATAATATAA[A/G]TACACATTAGCTGAG	51317
rs542220599	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45998073	ATATACATGTACCAC[C/T]GTGGAGAGAGGCTAA	51317
rs542224109	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071266	ATGAATACGCCCCAG[A/G]TAGCTGCTGTCCCTT	51317
rs542224177	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080158	TACTATATATTTATC[G/T]AACTACTAGTTTTTT	51317
rs542228894	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45966426	CTTCTAATATCTGTC[C/T]ACTTCTATCCTCACT	51317
rs542259559	snp	G/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46031377	AATGTAGCTCAGATT[G/T]ATTATGTCACTTCCT	51317
rs542274248	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45962179	TATAGACATCACATG[C/T]AGCATAGCAACTGGT	51317
rs542278989	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46024030	TGTGGGAACACTGAT[A/G]TTCTAAGGAACACAG	51317
rs542280455	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45981951	TTTTCTTTTTTTTTT[C/T]TTTTTTTTTTTTTTG	51317
rs542285898	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46118561	GTACAGAAATTTTTT[A/T]ATAAACATTAGCATA	51317
rs542302443	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067297	TAACAAGTATCTGAA[A/G]AGTCTAGAGGGTAAG	51317
rs542305860	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45953930	ATACGGTACAGGTTG[C/T]CCTTTCTGATTTCCA	51317
rs542339812	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062865	CAAAGACTTGGACAT[C/G]AATGTTCAAATTAAT	51317
rs542350485	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017217	CTCAGGTGATCCGCT[C/T]GCCTCAGCCTCCCAG	51317
rs542359903	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46018305	TTTCTTATAAAAGCA[C/T]CAAAATGTACCTCCC	51317
rs542373204	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037597	GCGGTGAGCCGAGAT[A/C]GTGCCAGCGCACTCC	51317
rs542384009	in-del	-/AAAA	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46029670	TAGAGCCTCCGTCTC[-/AAAA]AAAAAAAAAAAAACT	51317
rs542459213	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044977	TATGGTCATTTAAGG[C/T]CTTCTAGTACCAGGT	51317
rs542490467	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45974581	ATCTCATTCTCCTGA[A/G]TACCTTGGACTAAAG	51317
rs542508323	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079432	GGTGACAGTGGCTTC[C/T]GAAAGGAATTTAAGC	51317
rs542515075	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46100701	CCCCATGCATTGAGA[C/T]GGAATAATTACACCT	51317
rs542535545	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46020456	TACATACGCAGCGGA[C/T]GGAAGTGCTTACCAG	51317
rs542576936	in-del	-/TAGCT			intron-variant	PHF21A	GRCh38.p7	11:45966458	CACTATCTACTATCC[-/TAGCT]TATGTTTGGCTCACT	51317
rs542589753	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983245	GAAGCTTGGGGTGGG[A/G]GCTGGTGGGGGGACA	51317
rs542591419	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088299	ATCCAACAGCTCTAC[A/G]AGTCACTATCAGCAA	51317
rs542593264	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984600	GGTTCGTTTTTCCAC[C/T]GTTTAAGTCACGTTC	51317
rs542601433	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021529	TTGCACATGTGTGTG[C/T]GTGCATGTGTGTGTG	51317
rs542613216	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45945685	GGAAACTCAGAAGAA[A/G]GCTGCCTTACATGGC	51317
rs542622024	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45955574	GCAGCAGTGCTTTTA[A/G]GGAAGGGCAAATCAA	51317
rs542624090	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052829	TGGACATCTCTGACC[A/G]AGCCATCTTACCAGG	51317
rs542628966	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45950431	AGCAGGGGTGTCCAA[A/G]CTCTTGGCTTCCTTC	51317
rs542638371	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004706	ACTTTTACTGTGGAT[A/G]AGGGCTGTATCTGCC	51317
rs542639880	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029750	AGCAATAAATTTCAT[A/G]TCATTTCCAATAGTG	51317
rs542643362	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013279	AGTTTTAAACTGCAC[A/G]CTTAGAGTAGCCTGA	51317
rs542661159	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46061184	CTGTTTTTGTACCAG[C/T]ACCATGCTGTTTTGG	51317
rs542711383	in-del	-/CT			intron-variant	PHF21A	GRCh38.p7	11:45993706	AGATACAGTCAACTG[-/CT]CCAGGAAACAGAGTC	51317
rs542718745	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006803	AAAATATTTTAAGAC[C/G]AACAACCCTCCCTTG	51317
rs542755718	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013765	CTGTACTGAATACCA[C/T]AGGTAACAATGGTAA	51317
rs542770648	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46041721	TTTCAAACATACATA[A/G]AAGTTCATAGTATAG	51317
rs542801797	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45995774	CATATTCAGCTCAAT[C/T]ATACATGTGTAGACA	51317
rs542812319	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960497	GAACAGGTACATCTA[C/T]GGAGACAGAAAGCAG	51317
rs542839763	in-del	-/TTC			intron-variant	PHF21A	GRCh38.p7	11:46086616	GATTATGTATTACAG[-/TTC]TTCTTGAAAACAACA	51317
rs542847694	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978080	GCCGAGGCGGGCAGA[A/C/T]CACGAGGTCAGGAGT	51317
rs542848284	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46048585	GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCAT	51317
rs542863808	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988110	GGAACACTGCTCAGA[A/C]AAAACAAATTGTTTT	51317
rs542882712	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011994	ATCACCTTCTTTACT[G/T]CCTGTCCATCCTGGG	51317
rs542905840	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088952	TACTGCTAAGAAATA[C/T]TTTGCTGTTACTGAG	51317
rs542921448	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46011424	AGCCCAGTAGGTGGA[A/G]GTTGCAGCAGTGAGC	51317
rs542928761	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122191	AGCGGCCCCAACTCC[C/T]TCCAGTGCAACAGCA	51317
rs542951452	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46115663	TCATTAATATTTCCC[A/T]GCACAAAATAATATG	51317
rs542986458	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45978712	TCTATAGCTTTCAAC[A/T]GAGTCATAAAGGGAT	51317
rs543017058	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943795	AGATGAAAGTTAACA[A/T]CACCAACAACAGAAG	51317
rs543050172	in-del	-/A/T			intron-variant	PHF21A	GRCh38.p7	11:45977843	TTTTTCTTCTTCTTC[-/A/T]TTTTTTTTTTTTTGG	51317
rs543067136	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45996745	AAACAAAAGGTAGCT[A/G]TATTTATAACTCTGC	51317
rs543069415	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46095911	CATTCAAAGACACTT[C/T]AAAATGTCACCTTAC	51317
rs543071893	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46075742	CATTAATGATTCATA[C/T]CTCTTCCACATAATT	51317
rs543078270	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45951830	TTTTTTTTTTGAGGC[A/G]GAGTCTCACTCTGTC	51317
rs543078640	snp	A/C	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45943103	CTTCCAAGCTATCAT[A/C]ATCATCATCTTTCTT	51317
rs543087739	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053466	GTATAAATGAAATCA[C/T]TCTTAAGAGGATATT	51317
rs543102898	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45987496	GAAACTCCGTCTCTA[A/C]TAAAAATACAAAAAA	51317
rs543104560	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46047966	AAATGAAATATGTAA[C/T]ACTTTTTTAAACAGA	51317
rs543121072	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45945372	ACTCTGCTCTAAAGA[A/G]CAGAGTTTCTGCTCA	51317
rs543191947	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113414	TCTTACGTAGGAGAA[C/G]CACAGAAAAAAATGC	51317
rs543214781	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044125	TAGAATCAAGTTTCA[A/C]CCTAAGCACTACTGT	51317
rs543229357	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46103687	AAATTCTTGCTAAGG[A/G]TAACATATACCATAT	51317
rs543257773	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45949695	CTGTCCTACACGTGG[C/T]TCTCTGTTGAGAGTT	51317
rs543258638	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45934520	CAAACCGGCAGAGCC[A/G]CCATCAGACTTCCAA	51317
rs543268675	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46118598	CACAAAATTTCCTCT[C/T]TGCCATGAAAAGATA	51317
rs543301742	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961255	GCACAAACCTAGAAT[A/G]AAGTTAATCAAGTAT	51317
rs543329788	in-del	-/GT	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46049450	GTGTATTCCTGTACA[-/GT]GGCATCTGCAAGCCA	51317
rs543335087	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46069945	AACTCCATGCACTCA[A/G]TGGATACACGTGCAT	51317
rs543335617	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978023	ACAGAGATGGTGGGC[C/T]GGTTGCGGTGGCTCA	51317
rs543340913	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45951122	CTTTTCTTTGCTTGC[A/G]TGTGGTCTGAAAAGT	51317
rs543346610	snp	G/T	0.0119091	0.0762411	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120399	CCCCCGCCCCCGCCC[G/T]CAGCCCCCGGCCGGC	51317
rs543365810	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970665	TAAAGTGCCTCAACT[A/G]ACTCCAGTTCTTTCT	51317
rs543371259	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078074	CCCATCACCATGCCT[A/G]GCTAATTTTTGTATC	51317
rs543374951	snp	C/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46059989	CCTCAGGTGATCCAC[C/G]CACCTCGGCCTCCAA	51317
rs543376282	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036603	TAAGTAAAAGTAAAG[A/G]TACAGGTATACATTT	51317
rs543390817	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46095544	TGTCATACAATTTTT[G/T]GCAAACGGAAGATTG	51317
rs543425508	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45950889	TATACTGCCACAATG[C/T]TAACTCACAGCTAAA	51317
rs543427132	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978602	GGTGTTGGTTGTAAG[A/C]GGTATCCACGCTTAG	51317
rs543431164	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037587	CGCCTCTGTTGCGGT[A/G]AGCCGAGATCGTGCC	51317
rs543431847	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011404	TGAGGCAGGAGAATC[A/G]CCTGAGCCCAGTAGG	51317
rs543454321	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068915	ACTCAGGTAAAATGC[C/T]CTATAATAATGTGGC	51317
rs543487281	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46060927	GAGGTTATCTACCAG[A/G]GTTTTTATAGTTTTG	51317
rs543487344	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46051631	ACCAGCTGTTTTTAA[C/G]CATGCCAATGTGCAA	51317
rs543523856	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45973969	ATTCTACAAAATACT[A/G]ACTAAAGCCTCAAAC	51317
rs543550749	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45970454	AGCTCTTAGGTGCCA[C/T]TTTAAGGGAATTTTA	51317
rs543561876	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45942977	TTTCTAGTCAGTTAG[G/T]CCAAAAACTTTGGTT	51317
rs543584711	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45967633	GACAGCTGTAGGGAC[C/T]GCTGTATGGACTCAT	51317
rs543590286	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46088322	ATCAGCAAGGCCACT[C/T]GCCTAGCCCAAAATA	51317
rs543599802	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025972	AACACTGATACAATA[A/C]TATTATCTCCAGACT	51317
rs543609373	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45953742	ATATTCAAATGTGGA[A/G]CATATTAATAAAAAG	51317
rs543651351	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46081931	CTGTGTGTCCCTTTA[A/C]AAAAAAATTTGCTAA	51317
rs543657008	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46096623	TTCCCAACTCTCTGG[C/T]TACTCTCTTTGGTTT	51317
rs543658097	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45986233	CCTTTTATTTGCTAG[C/G]CTGATTGAAATGCAG	51317
rs543672581	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018742	TCAAGAAAACAGAGA[C/T]AGCAATTGATAGTTG	51317
rs543678012	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46031946	CCACACAGTTACCCA[A/G]TTTTCCCCAATGCAC	51317
rs543680012	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46034427	TTATCCTCTTATGTT[A/T]TTAGGTCCTTTCCTG	51317
rs543701313	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930631	GTTACCAGGATGCAG[C/T]GCCTGGACAGGAGCT	51317
rs543704333	in-del	-/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086123	GTTTTAGCTACTATC[-/T]TTTTTTTTTTTTTGA	51317
rs543748216	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46076928	AAGCAACCCGAAGCA[C/T]TTAGCCAATCAAATC	51317
rs543768715	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987428	GCACTTTGGGAGGCC[A/G]AGGTGGGCGAATCAC	51317
rs543771485	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46056308	GGGATTCAGAGAGTA[A/G]AACAGACTTTACATT	51317
rs543805706	in-del	-/TGTTGTTGTTAGTATTAT	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46033255	ACTGATTCCATTTTC[-/TGTTGTTGTTAGTATTAT]TGTTGTTGTTGAGGC	51317
rs543809793	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45960492	ATCCAGAACAGGTAC[A/G]TCTATGGAGACAGAA	51317
rs543832540	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949789	GGATGAGCTTTATCC[A/G]TAAGACTTAAACTGA	51317
rs543852881	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004600	TAAAAGTTTTAAAGA[A/G]CTGTGCTCATTTGAC	51317
rs543890174	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45994797	GTTCCAGTAGTAGGA[C/T]GACTTTGCAATATTC	51317
rs543901315	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112595	CTACATTTTCAAGTA[C/T]TAAATTTACACTAAA	51317
rs543935665	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099914	TAAAAACTAAAAATG[G/T]TTCCATACAATTTAC	51317
rs543941906	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45958288	CAAAGACACCAAAGA[A/G]TAGAAAATGGGCTGG	51317
rs543981439	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46121999	GCGGCGGCGGTGATG[G/T]GGCCGAGCACCGAGC	51317
rs544000342	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022469	CTTAAAAAAAAAGAA[A/G]AAGAAACAAAAAGAC	51317
rs544023073	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46056767	AGACCCTTAGAGAGG[G/T]AAACTTTAAGATTAG	51317
rs544034489	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46062828	GGCATTTACTGAAGA[G/T]AAATGAAAGCAGATC	51317
rs544039078	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46102688	TTTCTGAGGTAAAAA[A/G]GTATTTTTCTATTCT	51317
rs544039116	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46064005	TCAGAAAAACAAATT[A/T]CAAGTTCTGTCGATT	51317
rs544048155	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085493	TGAATGTGGCCTTAG[A/G]CATGATTTTAGGTAC	51317
rs544060256	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46010693	AGCCAGCGTGCAAAG[C/T]CTTGACCCACAGAAG	51317
rs544073759	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015123	GCATTTTTTCATGTT[G/T]GTTGACTGCTTGTAT	51317
rs544075765	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46099326	AAGAAAACTCCTGCT[A/G]CATCGATAGCCAAGA	51317
rs544082401	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068388	CATACATATATATAA[C/T]ATATGCACATTATTT	51317
rs544109623	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014474	GTGGCAATGAACATA[A/C]AAGTGCAAGTGTACT	51317
rs544110968	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46023058	GCCCGGCCTTGTTAT[C/T]TTCTATTATAGTATA	51317
rs544120597	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076249	TAATAACATTTCACC[A/G]AAGTTTTTTCACGTA	51317
rs544127041	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959693	AATTCAGCAAAGTTG[A/T]AGGGTACAAGATCAA	51317
rs544127182	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968354	GCCTACAAGGTTCCA[C/T]CAGCTCTGGCCCTAG	51317
rs544157615	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46086354	TTGATCTCCTGACCT[C/T]GTGATCCGCCCGTCC	51317
rs544165912	in-del	-/AAAAAAT	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45989992	GTGAGACCCTGACTC[-/AAAAAAT]AAATAAATAAAATTA	51317
rs544168577	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45961072	ATTAAGAATAAAAGC[A/G]GGATATCTGTTATAC	51317
rs544169180	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45947243	ATCTAAGTCAGGGCC[C/T]TTGTCTTCTAGGGGC	51317
rs544171267	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46064201	CATTCACTGTTCATA[A/G]GGAAAATTAAGTTCA	51317
rs544178629	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46106590	TTTGCACATATCCAA[C/T]TCCATCCACTGATAA	51317
rs544179424	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46074796	GCGTGAGCCACCGTG[A/C]CTGGCCAATAAAACT	51317
rs544209491	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46072958	TATCAGAATATCTCC[A/G]TAAAAGATCACATAT	51317
rs544216978	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45989053	GACAAGACACCCCTC[C/G]TCAAACAACAGGGAG	51317
rs544256086	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45956007	CAGACCAGAAGGAAA[C/T]GGGTTAATATATTTA	51317
rs544258755	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097513	TCTACAGCAGTTTCA[A/G]GAGCAAAAGAATACT	51317
rs544286672	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46108718	GCTTTTGTAATATTT[A/C]TTGAAAGGACACTTA	51317
rs544306544	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45938935	GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC	51317
rs544325298	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107867	TTTTTTTTTAACTGC[A/G]TTAAAAAATACTGAG	51317
rs544329798	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45989875	ATGGTGGCATACACC[A/G]GCAGTATCAGCTACT	51317
rs544338775	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45999582	GGAAATTTAAAAATA[C/T]ATCTATAGAGGACAA	51317
rs544372949	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45953859	ATGAATCTATAAATA[C/T]GAGTCTAAATAAGGT	51317
rs544379349	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45964130	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	51317
rs544417743	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45972839	GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC	51317
rs544440635	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45953077	TGGGGTTCTAATGTA[A/C]TACAATGGTTGTAAC	51317
rs544447672	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944762	ATGCCCTTAAATCCA[C/T]TCCATTTTTGATCTC	51317
rs544457891	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005957	AAACATACAATTTTA[A/G]AAGTTTATTTGGAGC	51317
rs544459231	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998483	TTTTAGGAAACAGAA[A/G]ATGTACATGCAAAAT	51317
rs544505984	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114541	AGTGACGGGCTACTA[C/T]AAAGGATTTGAAGCT	51317
rs544531480	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46020649	AATATGAACATGACC[C/T]AGAGTTCTCTATATT	51317
rs544541597	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46105715	GAAAAAAGCAAAATT[A/C]TCATAATTTTGTAAC	51317
rs544548707	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46082258	CTCAATTTCAGCCCT[A/T]ATCTCATTCCCTAAC	51317
rs544579728	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46063786	CAGGAACTGATGAGG[C/T]TTAGGGGCAGCACTT	51317
rs544600962	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46045327	TATTATACCAGGTAC[C/T]AACACAAAGGAGAGG	51317
rs544638100	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45936975	CTCAATTTTAGATTT[C/T]GATGTCCCTCAAAGA	51317
rs544652953	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46091477	TGCCCCACAATTACA[C/T]TTCTCTCTCTTTTTC	51317
rs544663480	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46022982	TCTCGAACTCCTGAT[C/T]TCAGGTGATCTGTCT	51317
rs544663577	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45984944	TCCATGAATCAACAT[A/G]CAATTTAAAAATACA	51317
rs544669205	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089816	GGAGGGGGTGGGGGG[A/C]GGGTCCTCATTTTTT	51317
rs544676843	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45980896	TGTGGCGGTACACAC[A/G]TTTGTTTAGGCAGAG	51317
rs544696638	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978156	AATACAAAAATTAGC[C/T]GGGCATGGTGGCACG	51317
rs544736767	snp	G/T	0.00755907	0.0610114	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930789	TCTCAAAAGTGGCTG[G/T]CAGAGCAGCTAAATT	51317
rs544743955	snp	A/C	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46106795	TCTCAATGGGAGTAG[A/C]AGCTATCAGGGCAGG	51317
rs544756769	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062812	AACCCAGACATACTA[A/C]GGCATTTACTGAAGA	51317
rs544756905	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089147	TATATTCTCAGACAC[A/C]ATGTTTAAAGTAGGT	51317
rs544790471	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45996932	CAAATGTATCCATTG[C/T]AAATGTTAGTCTATG	51317
rs544790966	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46071803	CATGATATAGCCAAT[G/T]ATGCTAATATTTAAA	51317
rs544829231	in-del	-/AAG	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46099040	ATTTTAAAAATAAAC[-/AAG]AAGAAGTTAAACTAA	51317
rs544850086	in-del	-/A	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46059067	AAGCTAGTTGGAGTT[-/A]AGATTCTACTATACA	51317
rs544851815	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46014413	TATCCAATCCACTGT[C/T]GATGGACACCTAGGT	51317
rs544896923	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945354	GGAACCTGTTTCTGA[C/T]CAACTCTGCTCTAAA	51317
rs544907190	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46095073	AATGAGGTTCACATA[C/T]CCAAAAAGAGGAAAT	51317
rs544908339	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46030392	ATGATTTGCCCAGGT[C/T]TTCATCATTTGTCTT	51317
rs544938060	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013852	CGAAAGATGAAAAAC[A/G]GTAAACCAGCTTGCA	51317
rs544971236	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45957780	AAAAAGAAAAAAGAA[A/G]ATAAAGTCTAGGATG	51317
rs544972967	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46072064	AAATAAAACAAACAC[A/G]TTCCCTGACTTCCTG	51317
rs544981029	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021575	TCAGAGACAGGGTCT[C/T]ACCCTGTCATCCAGT	51317
rs545004623	in-del	-/CTTTTGCC	0.0146672	0.084371	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934803	CCGGGGACTTAGAGT[-/CTTTTGCC]CTTTTGCCCTCAGCT	51317
rs545027353	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045141	CTGACTTAGAATGCC[C/T]CCATTCTTTCTGTTT	51317
rs545055327	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46104727	AAGATTTCCTCATTT[G/T]ATTGTCACATGAACC	51317
rs545077671	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45998985	GCACCTGCCACCACG[C/T]CTGGCTAATTTTTAT	51317
rs545092016	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116456	AAGAATCAGGGAACT[C/T]ACATACTCACTAAAA	51317
rs545119034	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053548	ATATATATAATTATA[C/T]GTATACCATGACTGG	51317
rs545140584	in-del	-/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45959094	ATCCCAAGAGTGGAA[-/G]GGTGGTTCAATGTAA	51317
rs545153484	snp	A/C			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934921	TGAGGAGGAGAAAGC[A/C]GGTAAGCAGGACAGT	51317
rs545163175	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007334	CTTTTTTTTTTTTTC[A/G]AGATGGAGTTTCACT	51317
rs545191358	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46019813	GCAACACAGAAGCAA[A/G]TAAGAAATATTACAT	51317
rs545227875	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930190	CAAGGGAGGCTCTGA[G/T]GGCCCCAAGAGAGAA	51317
rs545245216	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46089045	TAAGTCCATGACACA[A/G]TGTGCCCCAAACTGT	51317
rs545256236	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46022384	CACTTTAGCCCAGGA[A/G]ATTGAGGCTGCAGTG	51317
rs545259668	in-del	-/CT			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120337	GGAGCCCCAGCTACC[-/CT]TCCCCGGCCGAGGGA	51317
rs545284724	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961279	CAAGTATACTTTATA[C/T]ACTTGTCTGCATGAA	51317
rs545286809	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46080983	CTACTATTCTAACAA[C/T]CCTGAAACCCAGCTC	51317
rs545300091	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972712	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	51317
rs545300363	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963010	AAGCTCTATCAACGT[A/G]AAGGCCACGACAGGA	51317
rs545333264	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004936	AACAGATAAGCACTA[C/T]ACAACAAAGTTTACT	51317
rs545346056	snp	A/C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113497	TTTAAAGTTTGAATG[A/C/G]ATCCATTTCAACATT	51317
rs545355802	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089682	ATACTATTAAATTAT[A/T]TTTAATAATGTTGTT	51317
rs545360091	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972134	CAAAGATGCAATGAA[A/G]CATGACAAGGTGAAA	51317
rs545388261	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935926	GTATGCTAAAACTGT[C/T]AGTGGCTTGGGTCTG	51317
rs545409884	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45992806	AAATGGTAGTAATAC[A/G]TTTCATAATGGTGCC	51317
rs545449944	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944675	GTTCCCTCTGCCTGG[C/G]AGGCTCTTCCCCCAG	51317
rs545454991	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46116197	TATTTTTACACAAAA[A/C]TATTTCAGTGCACTC	51317
rs545460500	snp	C/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118843	AAAAAAGGAAGGAGG[C/G]GGCCAGTCTTCAAAG	51317
rs545461714	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110907	TCTCCTGCCTCAGCC[A/T]CCCGAGTAGCTGGGA	51317
rs545464213	snp	C/T	0.000135058	0.0082165	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928857	CTGAGGCTGGGCCGG[C/T]GCTGCCCCTCATCTT	51317
rs545476598	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097489	CACTCCCTCAAATTA[C/T]TGAGGAAATCTACAG	51317
rs545499674	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045620	GCACTACAATGTATT[A/C]AAAAAAAGAATGGTT	51317
rs545525744	snp	C/T	0.00103744	0.0227518	intron-variant	PHF21A	GRCh38.p7	11:45949368	TAAATAAAACTGGAA[C/T]ATGAGGGAAGGGCCA	51317
rs545528391	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105499	TAACCAGGAACTGCA[A/C]GAAATGGGCAATTCA	51317
rs545536170	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961978	GTAGATAAGGAAGTT[C/G]GTTATGTCTGACAGG	51317
rs545560556	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46096982	AATCCTAAAAGTCAT[C/T]TTAAGACTCTTCTTT	51317
rs545562842	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46020611	TCGGTCCTATTTAGC[G/T]CTATAAGTTATGAAA	51317
rs545565697	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45984799	GTCTCTGCTTTTTCA[C/T]ACATTCAGTCACTCC	51317
rs545570500	in-del	-/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46042235	ACATGACAAAACATA[-/T]TTCCTCAATAAGGCA	51317
rs545595653	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079266	TTTTAAGTTAACACA[A/C]AAAAAAGAGCAACAC	51317
rs545629813	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070116	TCCTTTGTTTCAGTT[A/T]CCTAATTAGCTTAAA	51317
rs545650852	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46091176	AAAAGGAAACCTTGG[C/T]CAAATATCTACTATA	51317
rs545653291	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067197	GTAAGGGGGTCTGCC[A/G]GAAGAAAGGTATAAG	51317
rs545655370	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017129	GCATGTGCCACCACA[A/C]CCAGCTAATTTTTGT	51317
rs545680309	in-del	-/A	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46069982	CTCAATGCATAATCC[-/A]AACATTCCACGAATA	51317
rs545690044	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074944	GTTCCATCAAGAAGG[C/T]TGTTTTAACAGTTAA	51317
rs545696480	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46038128	TTCTCTCTCTCTCTC[-/T]TTTTTTTTTTTAAAT	51317
rs545733820	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46000915	ACAAAAGTGAACCTC[C/T]GTCTCAAAAAAATAA	51317
rs545734519	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042073	ACATTTTCTGGAACA[C/T]AACCATTGTCTATAG	51317
rs545737927	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46118390	ACTGTAAATACTATT[A/G]TGTTACCAAAAGCAA	51317
rs545777184	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050408	CTGACTGTGAGCATG[C/T]TGGGGAGAGCAGGAG	51317
rs545779564	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46070520	ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCATGTT	51317
rs545783367	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933437	CCAGCCACTCCCCTT[C/T]CCTCTTCTGGGCACT	51317
rs545817095	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009715	TCCAACTTGGGCAGT[C/T]TGGCTACAGAGCCCA	51317
rs545818066	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973517	TTCTCTTTGCCATTG[A/C]CTCCTTAAATGTGAA	51317
rs545819681	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46064262	GGTCAAAATGATACA[A/G]TTTGTTTGGGCAAAG	51317
rs545839497	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974489	GACAGGGTCTTGCTC[G/T]GTCACCCAGGCTAGA	51317
rs545848202	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46105982	AGGCACGGATTTAAT[A/T]TTTGTATACTAACAT	51317
rs545864427	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049958	TCAGACCTGTGATTA[A/G]CTCAATCAAAGTAGG	51317
rs545870503	snp	A/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46093279	TTCCTTTTGCCTTAA[A/G]TATGGTGTTTGTTGA	51317
rs545892554	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46082653	AACTATATCCCTTTT[C/G]AGTCAACAAATGTAA	51317
rs545902634	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983156	AATCAGAACCAGAAT[C/T]AGGAGCGTGGGAGTC	51317
rs545904756	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041023	CTAGATTTGAACATG[A/C]CTCTACAGTAAATAG	51317
rs545908883	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46066482	GAGTCAGAAGGATCA[C/T]TTGCCAGGAATTCAA	51317
rs545922097	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46083649	TACTCTGTTTACATA[A/C]CAAATTTTAATTATG	51317
rs545930954	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45984259	CTTCTTAATATATTT[A/C]TATAAACAATAAGCC	51317
rs545955481	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930888	GTGTCACGAGCGTAT[C/G]TCTCAGGTGGTCACA	51317
rs545962664	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092446	ACTTTTCCATAGTTT[A/T]TCAAGACAAGCAAAA	51317
rs545969957	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46106066	AACCTGACACAATGA[A/C]AACAGGAACTATTGC	51317
rs545978083	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46087608	GAGACTGGTCTGTGC[A/G]GAAAGAAACAAATTA	51317
rs545983257	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057441	CCCAGAGCATTAGGG[C/T]TTAATTTTCCCAATG	51317
rs545992015	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46082770	ATTCAGAATATGAAA[C/T]AAAATATTTAGTAAT	51317
rs546014169	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45957216	TATCCCTCTTTAAGT[A/C]ATGGATAAAACTTGT	51317
rs546016534	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938090	ATTTCCCCGGGAAAG[G/T]AATTCCTCCTGATGG	51317
rs546035312	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056162	CTCCGGTTTTGAATT[C/T]CATCTTATAAGGAGA	51317
rs546043143	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46090977	TTCTCTAAGATTCCA[C/T]CCCATGTCAAAGTAA	51317
rs546044809	snp	A/C	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46110042	ACTAATTTTTTGGTT[A/C]TAACTCATTATTTAA	51317
rs546064421	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45966302	AGACTCATCAATTTC[C/T]TCTTCCAATCTTCTC	51317
rs546092368	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931305	CCCCCAGATGGGCCC[A/T]GACAAGTTGAGGGGA	51317
rs546105387	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058330	GCTTAACTGTGTCAC[A/C]TTGTTGGTAAAACGA	51317
rs546118994	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46031663	TTCTCTTTAGATTAA[C/T]AGGCGCTCCGAGGCA	51317
rs546119915	snp	A/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46047286	TTAGTGAAAAGTGAC[A/G]TAAGTGGTTACTATT	51317
rs546127682	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45939880	GATAAGAACACCAGG[A/G]AAGGGAAGACTGAAG	51317
rs546136163	snp	A/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46100270	CCATTAACCTTGTTT[A/T]AAAAAAAAAAAATCC	51317
rs546208826	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023287	AGAGAGACAGCTGAT[A/G]GCTAATTACTGAGGC	51317
rs546214756	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46030622	AAATTCAAAAAGATT[A/C]TTTAATCCTAAAACA	51317
rs546231075	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46061943	GGACTTGATCAAGAG[A/T]TGGGTTGGGTATAGA	51317
rs546237617	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46027206	ATTATATTTCAAAGA[C/T]GATGCACTGATTTCT	51317
rs546257420	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46102103	CCTTGTGATCCACCC[A/G]CCTCGGCCTCCCAAA	51317
rs546262307	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46090330	ATAATGCAAGTGGGT[A/G]TGGTAGTCTCAGCAT	51317
rs546264721	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991088	CTTTTTACTGCCTCC[A/G]TAGTTCTACCCTTTC	51317
rs546319825	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46100039	GTCAATGAGAAGTGG[A/G]AACAGCTACAATACA	51317
rs546321063	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023981	AAACAAAAAGAATCA[C/T]TGAATGGCATAGAGC	51317
rs546330490	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048052	CAATGGCTTTTAACA[C/T]ATTCACAGTTGCACA	51317
rs546359136	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107729	TCACTAATAATCTCA[A/G]CAACAAGTTAAAACT	51317
rs546362968	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929565	ACCTCTGGCCTGCCC[A/G]TCCCATCCCGCCTGA	51317
rs546392495	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46044327	AGAAAATTCATGCAA[A/G]GTAAAAGAAGTAATT	51317
rs546423550	in-del	-/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46012526	CTATTTGGTCTTACG[-/C]CAAGTTAACTCACGA	51317
rs546454590	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998754	GGACCTCAAGTCATC[A/C]ACCTACCTCGGCTTC	51317
rs546459925	in-del	-/A	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46028846	CAAAGTGCTGGGATT[-/A]CAGGCGTGAGCCACC	51317
rs546473270	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45998544	TTAAACAGAGTTTTG[C/T]TCTTGTTGCCCAGGC	51317
rs546476833	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997552	AGATCCAGTGACAAT[C/T]AGATTTCTCCTCTGC	51317
rs546487493	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46055158	TTGAAGCAATCTGAA[C/T]GTAGAATCCTTCTGG	51317
rs546496698	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46025701	AAATTCCCCAAAAAT[A/G]TTATCTTTACCACAT	51317
rs546506421	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45974895	ACCCAAATTGCATGA[A/G]CTAGAAGTTAATGCA	51317
rs546508042	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46114914	TTCTGTGTTTAAGTT[A/G]TTTTTCCCCTAGGCC	51317
rs546590734	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972202	GATGAACTGAGGTGA[A/G]AGGACTTGACTGATG	51317
rs546603369	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099941	TTACATTTTTTAAAA[A/G]ATCTTTGTAGTCCAA	51317
rs546607339	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45981988	TTGAAACAGGGTCTG[A/G]CTCTGTCACCCAGGC	51317
rs546621414	in-del	-/AA/AACAAA/AAG	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46088420	AATAACAACAACAAC[-/AA/AACAAA/AAG]AACAACAACAACAAC	51317
rs546635273	snp	G/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46083184	AAAAAAAAAAAAAAG[G/T]ACACAGCTTATTACC	51317
rs546644304	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939063	GGTCTCGATCTCCTG[A/T]CCTGGCTATCTGCCT	51317
rs546653895	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007129	CCAACCAACCATAAC[A/G]TGACGAGACATCTAT	51317
rs546659858	in-del	-/A	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46107185	TTTGACAACATGCAT[-/A]AAACACTAGTTTAGA	51317
rs546699747	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45939998	TGTGCACAAGAAGCA[A/G]TAATAGAGAGGAATG	51317
rs546720884	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091258	TTTTAAAAAGGAGTA[A/G]TCTTGCACTAGGCGA	51317
rs546743760	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973237	ACTGGACAGTGGAGA[C/T]AGACGGTATTTCCAA	51317
rs546748920	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46018615	ACCTATTTGACTCAA[C/T]TTCATATGGAAGAGA	51317
rs546768224	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946665	CAGGTGTGAGCCACC[A/G]CACCTGGCCGAATTT	51317
rs546768524	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45937674	TTAGTAGAGATGGGG[A/T]TTCGCCATGTTGGCC	51317
rs546772207	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46097152	AGCCTCCTAACTGGC[C/G]TCCCCAATTCTACCC	51317
rs546814977	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45958989	TAAATGAAAAACCCT[C/G]AACAACAACAAAAAT	51317
rs546848495	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990618	GATTCATGCTTTTAC[G/T]GTATTGTTCTCCAGT	51317
rs546855624	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45971624	TAGTAATAACTGCAG[A/T]CTAATTCAGGCACAG	51317
rs546868938	in-del	-/T	0.320168	0.239951	intron-variant	PHF21A	GRCh38.p7	11:46016972	ATGTTTAACCTGGAT[-/T]TTTTTTTTTTTTAAT	51317
rs546886839	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107971	CACATGAAGTTGTGA[A/G]GACCAGGACTAATTC	51317
rs546887174	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46098990	CAAGATAATTCAAAT[A/G]AAAGTCACTAAGAAA	51317
rs546906206	snp	A/G	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929081	CCCTTTTTCATAATT[A/G]AAGTTTTAAAACATC	51317
rs546916873	snp	A/C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45979142	CTGCCTCAGCCTGCC[A/C/G]AGTAGCTGGGATTAC	51317
rs546963349	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021951	GGAACAGAAAATACA[C/G]GCATTGCACTAGTAG	51317
rs546971407	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45985495	TTAATGCAAGTAAAA[C/T]TCAATAAGAGAATCT	51317
rs546994224	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46029458	ACGGGGAGGCCAAGG[A/C]GGGCAGATCACTTGA	51317
rs547001554	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46030123	AACGCTAAACAATAG[A/G]GCAAACTGCTGACTC	51317
rs547023039	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46088799	TATATCTAGAAGACT[A/G]TAGGCTTTTCTGTTC	51317
rs547089940	in-del	-/AACAGAGTTACAAA	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46033799	TGTTTACTTTTTTGT[-/AACAGAGTTACAAA]AGGTGGCTGCTAGAA	51317
rs547100362	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076445	GATTCTCTATCACCT[A/G]TTCTCACTAACTGCC	51317
rs547109436	snp	A/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45963345	GAATTGTTTGAATCC[A/G]GGAGGTGGAGGTTGC	51317
rs547113917	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46063269	GTACATACAGTCTAT[A/G]TACAGTGTAGCACTC	51317
rs547133986	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929646	GTCCAAAGGCTGCTG[C/G]GGAAGGGGTAGGGGG	51317
rs547169314	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092821	CAAGTGCAGTGGCAC[A/G]ATCACAGCTCACTGC	51317
rs547171266	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038058	CTAATTCACCTTCTT[A/G]CAGAGCCCATTTTGT	51317
rs547199339	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45936099	CCTGGGTGACATGGC[A/G]AAACCTGTCTCCACC	51317
rs547222033	snp	C/G	0.00014929	0.00863844	intron-variant	PHF21A	GRCh38.p7	11:45946127	GGAAGTGAGGTAGCA[C/G]ACAGAAGGTTAATTC	51317
rs547229356	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089262	ATATCAGGTTTCAAT[C/T]TGTACAAAATACTTC	51317
rs547253329	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967281	GCTGAGACATAAGGA[C/T]TGCTTGAACCTGGGA	51317
rs547258534	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45935399	CTGAAAATCCTCTCT[A/C]TGATTAAAGCCAAGA	51317
rs547273195	snp	C/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45975869	CTCTTAGCATCTCCC[C/G]CTGGCCCCCCGATTG	51317
rs547286655	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984475	AAGACAGGTAGTCAC[A/G]GTGATCAATATTGTG	51317
rs547335507	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038498	CTAGGTTCTTGAAGG[A/C]GGTAAAGGAGTCAGT	51317
rs547335771	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46006335	ATTCTTAATCTTTCG[A/G]TTGTATATACAATTA	51317
rs547344083	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940126	GTAATCCACTAGGGT[A/G]TCTGGCAGCCCAGAA	51317
rs547358876	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058734	TAGCCATGTCTGTAC[C/T]AGTAATATGGTCCCC	51317
rs547393826	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45967847	ATCAGCATGTGCCTA[C/T]AGACATGTATCTCTA	51317
rs547405449	snp	A/G	1.64746e-05	0.00287002	intron-variant	PHF21A	GRCh38.p7	11:45948844	ACACACACACAAAGC[A/G]AAAGCAACAGCAGCA	51317
rs547431480	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46118591	AACTGTACACAAAAT[A/T]TCCTCTTTGCCATGA	51317
rs547432742	snp	A/C	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:46011497	ATTCAGTCTCAAAAA[A/C]AAAAAAGTGTTCAAT	51317
rs547445596	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026354	ATCCATGATGTAGAT[A/G]TCATGCACAAGGTAC	51317
rs547453978	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101478	TTAGGGAATAGGTAC[A/G]TGGGGTTATATTATT	51317
rs547478685	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940820	CAGTGATGGAGTGAA[A/T]GAGACAAACTGGGCA	51317
rs547512425	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46069108	CTACATATATACAAC[A/C]TCTCGATCTTCAGAA	51317
rs547514647	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059606	CTTTTTAAATTTTGT[A/G]TAGAGGTGGGATGTT	51317
rs547521934	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46035494	AGAGAATATTCCCTT[C/G]AATAGGCAGGTGGAG	51317
rs547522882	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46042802	ACCTTCTTGCTATGT[C/G]CTCACAGCAAGAAGG	51317
rs547525519	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992973	TAAAGAGCTGTAGAG[G/T]AGAGGTCAGAAAACT	51317
rs547551114	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46068682	GGAAAAAAAAAATAC[A/G]GTAGATTCCAGTCAG	51317
rs547558292	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46050106	CACTAGGGATTGCCA[A/C]TGAAAGGAAATGCTT	51317
rs547566929	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46033852	TTCTGTTCTATTTCT[A/G]TTGGACAGTGCTGCT	51317
rs547652435	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042394	GTGATAGTGCAACTC[C/T]GGAAAGTTCATCACC	51317
rs547665139	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45948155	GATGTATTACTGACA[C/T]CAAAGAAAAATTTCA	51317
rs547683826	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46066802	CACTTCTTAGAGGCA[A/G]TCACTGTGAATGGTT	51317
rs547688133	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46025531	ACAAAAGAAAAATTC[C/T]TTTACCTGAGAAGAA	51317
rs547718078	snp	C/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46065634	ATACAATTATAACAT[C/G]TATATTACAGTTGAG	51317
rs547734691	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049625	TCCCACCTGTCACAG[A/C]ACTCTCCTTGCTGGT	51317
rs547749552	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45957711	AAATCAATAACCTAA[C/T]TTTACACCTTAAGAA	51317
rs547763105	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46109397	TAAGGTACAAAAACC[A/G]TTCACAACTTGTCAA	51317
rs547775789	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016653	TGACATAATCTATTT[C/T]ACACTGCAATTTGTA	51317
rs547779174	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057629	AGCTGAAATAAGTAA[A/G]ATCACCTAAAACCCT	51317
rs547787967	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46001288	TTCTGTGACCACCAG[G/T]GGGGCTGGAAATGGG	51317
rs547789464	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46117603	TTTCAACACACTATA[A/C]CCCTTTCCAAAATCT	51317
rs547789832	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010155	AAGACAAAAACTAAA[A/G]CTCTCTCCTGATATA	51317
rs547814742	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966541	TTGGGTTCAAATCCT[A/C]GTTCTACCACTCACT	51317
rs547843629	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983556	CTCTGTCACTTAAAT[A/G]TAGATGACTGCACTT	51317
rs547888318	in-del	-/CG	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46072810	TCAGGCTGGGGAAAC[-/CG]AAGCTGCAACCACGA	51317
rs547888945	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041606	ATTCCAAAGGTACAG[A/G]TCCTACCCAATTTGT	51317
rs547901680	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017594	GGGGAAAAAAAAAAA[A/C]CACCTCCCTCATCTC	51317
rs547908724	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45992367	GAAACCCCGTCTATA[A/C]TAAAAATACAAAAAA	51317
rs547914535	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46035266	ATTTCCTGAAAAAAA[C/T]CCATCTTTCTCTACT	51317
rs547959174	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015617	TATAAAAATACTTTT[C/T]TTATCCTTATGTTTT	51317
rs547972425	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45965801	GAGGTCCAAACCTCA[C/T]CCTAGAACATAGCTT	51317
rs547997163	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45971574	TAGTTTTCAAGAGTT[A/C]TCATATTGGTGTCAC	51317
rs548020954	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967147	GCTGAGGCTGGTGGA[C/T]CACTTGAGGCCAGGA	51317
rs548041817	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45967790	AACGACCCTGTGGTG[A/G]GTGCTACTGACTTAA	51317
rs548055137	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932903	GCTTTTCTATTCCTT[A/T]TTTTAGTTTTTGTTA	51317
rs548077443	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46104581	TACTCTTTCTCACCA[C/T]GCATTTCAAGGGAGA	51317
rs548107887	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983505	CTGTGAAAAAAAAAA[A/T]TTTTTAAATCAAGAT	51317
rs548109052	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45956647	ATGTTTACTGTAATC[C/T]CCAAGGTAACCACTA	51317
rs548118663	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:45940043	CTATGATGTAATCCC[C/T]CCACCACCACTAGTG	51317
rs548128212	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101423	CTGTTATGTTTTACA[C/T]ACTATAAATAAAGAT	51317
rs548130483	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116923	AGTGAGCCGAGATCA[C/T]GCCGTTGCACTCCAG	51317
rs548143525	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085866	TTCTCATTAGGCATA[A/G]AACATCAGCAGAAAT	51317
rs548154896	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46117437	TACCACTGATACAAC[G/T]TGACTTACAGTTCAA	51317
rs548231741	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084971	AGGCGTGAGCCACTG[C/T]GCTGAGCCAAAATCA	51317
rs548249174	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45991366	GATATTACTTGCCAG[A/G]TAGAACAATGAGGCT	51317
rs548249525	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46109219	TACCTATGTGATCCG[A/G]GGGAAACCTCTACTT	51317
rs548263294	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46067729	TAACATTCAAAAACA[C/T]TTGCTGCTCATCTAC	51317
rs548270304	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46071050	TTTTAGACTAAGTGC[A/G]GTAGATGAATTACTG	51317
rs548273507	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45948813	CTATAATGATGGGAG[G/T]AGGGAAGGAGAAGAA	51317
rs548286230	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958664	TTCATGCCTATAATC[A/C]CAACACTTTGGGAAG	51317
rs548315632	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46117509	ATGTATTTATAAAGC[C/T]GAGTGCCTAAAAATT	51317
rs548338163	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075680	AATAGGAGGGAAGAA[A/T]ATAAAGCAGTTGTTC	51317
rs548344689	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45993634	ACTGAATGCAGAGTA[C/T]ACTAGTATGGGGAGC	51317
rs548396730	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46081707	CAGAATGCGGCAATA[C/T]TTCTTGAGGATATAC	51317
rs548400386	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009220	CTCAGGTAATCTGCC[C/G]GCCTCGGTCTCCCAA	51317
rs548408882	snp	A/G	0.0134861	0.0810011	intron-variant	PHF21A	GRCh38.p7	11:46031599	GTTGATAATAAACAT[A/G]CATAATTAGGCAGTT	51317
rs548422828	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46066541	TGTTTCTAAAAAAAT[A/C]AAAATAAATTAGCCA	51317
rs548427802	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073717	ATTTCAGAGCACATT[C/G]CTGTATCATTAAAAT	51317
rs548449065	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032487	ACCAAATGTTTTTTT[C/T]AATTCTCCACTATTA	51317
rs548451751	snp	C/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45955629	ATGGTTCAAATTTCT[C/G]TCTCTCATGCAAGAA	51317
rs548466764	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084277	CAGCCTCTGTTTAAA[A/G]TAACAAACTCCTCTT	51317
rs548484554	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46014265	TGAGAACATATAATA[C/T]TCAGTTTTCTGTTTC	51317
rs548486557	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042291	AACCAAACTTTAAGA[C/T]TGCTGGACAGGTATT	51317
rs548503938	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46073197	GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC	51317
rs548520492	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46118562	TACAGAAATTTTTTT[A/G]TAAACATTAGCATAA	51317
rs548522089	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944314	CCTTGTTCCCCTAAA[A/G]TAAGTGTGTATGGTA	51317
rs548557673	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008621	GGTGGAAATGTGACT[C/T]GGTTTTGTGTATGAA	51317
rs548645527	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973554	GTAAACGCGGAACAC[C/T]GATATTTATTTTGGG	51317
rs548654445	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45959819	AGGGTCTAGTATCCA[G/T]ATTATATAAAGAACT	51317
rs548657239	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944894	GCCTCAGCCTCCAGA[A/G]TAACTGGGATTACAG	51317
rs548661529	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45939245	TAGAGGACAACCTAC[A/G]TATCATAAATCTTAC	51317
rs548675416	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104336	TGCCTAGTCTACTAC[C/T]GACTTGATTCTAAGA	51317
rs548682448	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45972607	ACATGGCGAAAGCCC[A/G]TCTCTACTAAGAATA	51317
rs548695537	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46048654	ATACACCTGTAATCC[C/T]AGCTACTCGGGAGGC	51317
rs548720099	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122411	ACCCTTGAACCACTT[C/T]ATTAGCAGTACTTAG	51317
rs548742028	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46054012	TTTGCCCCCACTTCG[C/T]CACAAGCTTTTTCAC	51317
rs548757591	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46022917	CACCACACTTGGGTA[A/C]TTTTTGTATTTTTAG	51317
rs548808026	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46030913	GGAAGTGGAGGAGAC[C/T]GACCAGAGAAATTGC	51317
rs548816661	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45996446	ATGCTGGTTAAGAAC[C/T]AGCACTAAGTCTGTC	51317
rs548838114	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46104292	ATGGACTGACCAGCT[C/G]ATGAGTATTTAAGAC	51317
rs548845766	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45951574	CTTTGTGGTTGCCAA[A/C]TAACTACATTCCTAA	51317
rs548859825	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070480	GTACTACAGGTGCCC[A/G]CCACCACACCCAGCT	51317
rs548877051	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46100581	GGTCCTGTTAAGTAA[A/G]TATACTCCTTGCACT	51317
rs548908728	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45968910	CACTCCAGCCTGTGC[A/G]ATGGGAGCGAAACTC	51317
rs548925119	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014829	ACTAAAAATACAAAA[A/C]ATTAGCTGGGCGTAG	51317
rs548932537	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:46062247	GAATTATATGCCCTT[C/T]GGTTGTGGGACATTT	51317
rs548937827	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929921	CCTGCCAGGGGTGCC[C/T]GGCAGAGGGACAGGG	51317
rs548977894	in-del	-/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46087764	AATATTTTGAAAAAA[-/T]TTTTTTCCTGAGATA	51317
rs548996790	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005200	AAAACTTTTTGAGCA[A/C]TGACGTGATGCCACA	51317
rs549006005	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46000924	AACCTCCGTCTCAAA[A/T]AAATAAATAAATAAA	51317
rs549009580	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46043159	CCTTTAGAGGTAAGA[A/T]ATTCAATCAATGTAA	51317
rs549023069	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46117569	CCGAGGGGAAAAAAC[C/T]ACAAGAAGTCTAAAA	51317
rs549034699	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45997588	AACATTTTTCATTTC[C/T]CAATGAATAGAATTT	51317
rs549045069	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053909	ATTACAACCCCTCCA[A/G]TGAGATTCCAGGCTT	51317
rs549070169	snp	A/C	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46113959	TTCTAATATTGCCCA[A/C]CAGGAAATAATTTTT	51317
rs549078716	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044560	CTTCTCTTACTCTTT[C/T]GGGCAACCCAGATTA	51317
rs549111508	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46006128	TTTACGATTAAAGAA[C/T]CAGATTAACTGACAA	51317
rs549158300	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46019210	AAAAGAAGAAACTGC[C/T]TTTTAATTCTTTCTA	51317
rs549172076	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46096405	TCTAATTCCTCTCCT[C/T]CCAATCTCTATTGAA	51317
rs549184318	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087716	AGAGAAGGGGTCTCA[C/T]ATGTTGCCCAGGCTG	51317
rs549197623	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018436	TCTGGTGTATTTGGC[C/T]AGTTGGGAAAAATCT	51317
rs549202040	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010386	ACAATCTTGTGAAGA[C/T]ACTTTACAGAAGAAT	51317
rs549240134	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46087577	AGAAAGATCTCTTTC[C/T]GGATAGTAATTTTAA	51317
rs549263759	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119697	TACCAACCCCTCCCC[G/T]ACCAGGGCCACCTTG	51317
rs549275517	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46039209	AGAATACTAATGAAA[C/T]GTTTAAAAAGTTATC	51317
rs549278829	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46084066	GACAAAATTGTCTTA[A/C]AGATTATTAAAAACT	51317
rs549300766	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970020	TCTACAAGCTTTCAT[C/T]GTAAGTTAATCATCT	51317
rs549313358	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46035254	TGTTCTTATACCATT[G/T]CCTGAAAAAAATCCA	51317
rs549316344	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PHF21A	GRCh38.p7	11:46121170	CCTCTCCTCTCCTCT[C/G]TCTCTCACTCACTCT	51317
rs549333413	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934720	GAAGTGAGACGACAG[A/G]CCAGCAGCATTTAGG	51317
rs549364408	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46051919	TAAAATATCCAAAAA[C/T]AGCTTTTCTATCAAG	51317
rs549383613	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985569	TAGAATTCTAACAGA[C/G]GAAGACAGGGAGGAA	51317
rs549383925	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46103155	GGACAAACTGATTTT[C/T]AAAATTGTATAATTC	51317
rs549436117	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995200	TATTTGTTGTCTGAT[A/G]GGATACAGTGGAACG	51317
rs549465749	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977479	TACTTGAACAGGATG[C/T]TTCCATGGGTTAAGA	51317
rs549467773	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45951544	TTTCTAAACTGTATG[C/T]TGAAATGACATACAC	51317
rs549492104	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45942466	CCTTTGGCAATACTT[-/C]CAACTGAGAAAAAGT	51317
rs549501868	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122366	CGCCCGCTCCCTCCC[C/T]TCGCCACCCCGCCCC	51317
rs549507637	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45941184	GCTTACTGCAGCCTC[G/T]ACCTCCCAGGCTCAG	51317
rs549528983	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46069146	ACTTGCAGCCAGTTA[C/T]TTCTGAGCCTTTCCT	51317
rs549540812	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085991	CACATTTGCAAAGGA[C/T]AGGAAAAATTTACTG	51317
rs549545622	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45986327	ATATGTATGACTATA[A/G]AAGACTAATATTGAT	51317
rs549551802	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949952	TCAGAAAAAGAAGAG[C/T]TCCCCTAAATGAACA	51317
rs549560542	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059064	GATTAAGCTAGTTGG[A/G]GTTAGATTCTACTAT	51317
rs549607056	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068462	CTCCTAAAAAGCATT[C/T]GTTATTCACACTGCC	51317
rs549613160	snp	C/T	3.29527e-05	0.00405898	intron-variant	PHF21A	GRCh38.p7	11:45949353	GCACTGAACAGCTCA[C/T]AAATAAAACTGGAAC	51317
rs549615036	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959773	CAAACTACGGAACAG[A/G]AGAAAATATTTGCAA	51317
rs549618844	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004220	TGCATACTGGTAAGA[A/T]ATTTCATCCAATGTT	51317
rs549620490	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46077488	ATTAAAGTTTTCAAA[A/T]GCTTAATGTAGCAGG	51317
rs549668435	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102107	GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC	51317
rs549702146	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46086792	GTTCAATTCAATTCA[C/T]ATAAACTCTGGAAAT	51317
rs549708273	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968104	GGATACTCCATGTAA[A/G]GTGCCTAGCATAGTA	51317
rs549728655	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050934	TGTATGCTACACAGA[C/T]TTTTTTCTAGTAAAT	51317
rs549814207	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005048	ACATGCATGTATACA[C/T]CCAACTAATACAGCA	51317
rs549818405	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45956763	ACAGGAAATGAAGAA[C/T]AAAAAACGTAAGATA	51317
rs549838274	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46061504	TTGTACAACATTTTG[C/G]TATTCCTGGAACTTA	51317
rs549851001	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46012272	CTATTACTGACCATG[C/T]TCTTCTTGGGCCTCT	51317
rs549853316	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45972259	AGCTGTACTTTTCTA[C/G]ACTTTTTACTAGAAT	51317
rs549894060	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052200	CAAATAAAAAAAACT[C/T]TCCCTCTTCAATGGA	51317
rs549919634	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46078161	TTCTCACGGAAGTAG[A/G]ATCATTCAAAAGGAA	51317
rs549938359	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45941134	GACCGGGTCTGGCTC[C/T]GTCACCCAGGCTGGA	51317
rs549946442	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46110046	ATTTTTTGGTTCTAA[C/G]TCATTATTTAAAATT	51317
rs549961729	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026547	GCTACCTCTTCTCTA[C/T]CCTGTTCGCCCCTCA	51317
rs549962490	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985239	CCAATATTCATCAAC[A/G]CTGAGGATGCAGGAA	51317
rs549970742	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46093979	AAATTAAGAACTTCT[A/G]CTCATCAAAAAAACA	51317
rs549993491	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46042807	CTTGCTATGTCCTCA[C/T]AGCAAGAAGGTGCTA	51317
rs550009694	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102063	GGGTTTCATCATGTT[G/T]GCCAGGATGGTCTCA	51317
rs550033487	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968848	AGGAAGGAGAATCGC[C/T]TGAACCTGGTGGGTG	51317
rs550048688	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933890	ACTTTCCAGAAATCC[A/G]GCTTTGCTTTTCTAG	51317
rs550049230	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46116792	ACATGGTGATACCCC[A/G]TCTCTACTCAAAATA	51317
rs550051693	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058850	GAAGATACAAACATG[A/G]GAACTTCGCAGGGAC	51317
rs550085879	in-del	-/CACACG			intron-variant	PHF21A	GRCh38.p7	11:46114100	CTACACACACACACA[-/CACACG]CACACATCCCCACAC	51317
rs550092843	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45946597	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT	51317
rs550095208	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977388	GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGT	51317
rs550119710	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941762	GGTAGGTAAGTTGAA[A/G]AACAGCTGGCCCATG	51317
rs550120730	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46075645	CTGTCTGTGGAGAAG[A/C]CAAGATGGGGACGCA	51317
rs550121734	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042464	GACACGTTATAAGAC[C/T]GGACTAAAATCACTG	51317
rs550122245	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46027132	CTCCCAGATTATAAA[C/T]AGGCTGCCAATCCAA	51317
rs550125452	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46082326	TCGTCAAATGTATGT[C/T]CTGGCTTTGGTCTCA	51317
rs550129062	in-del	-/ATCTATCT	0.121675	0.214552	intron-variant	PHF21A	GRCh38.p7	11:46015903	TACAGTCATCTATCT[-/ATCTATCT]ATCTATCTATCTATC	51317
rs550129842	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46002669	TTTAAGGGATATAAT[A/G]AAGAACTTTGGACTC	51317
rs550133266	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930480	TTACCCCAAAGGGCC[C/T]GATAAGGAAGGAAGA	51317
rs550136140	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101679	GCTTTGTTGCCCAGG[A/C]TGGAGTGCAGTGGCA	51317
rs550174941	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110511	GTAATCACATGGGTA[C/G]ATATAATGATAAAAA	51317
rs550179268	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45993104	TTTAACTGGTTCTCA[C/T]TTCTGAGTACTCTGA	51317
rs550189344	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111204	CCAGGCGTGGTGGCT[C/T]ACGCCTGTAATCCCA	51317
rs550200592	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46092021	GTTTGAAGTATAGCT[A/T]CGTGAAATTAGACAA	51317
rs550210497	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46010362	ACATTATGTTACTTA[A/T]ACCTCGCAACAATCT	51317
rs550236602	in-del	-/AATTTGTAGAGAT	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46078239	TAGACCTGAGTTCTC[-/AATTTGTAGAGAT]AAGTGTTATTTTTTT	51317
rs550238399	in-del	-/AAAAAGAAAC			intron-variant	PHF21A	GRCh38.p7	11:46022467	CTCTTAAAAAAAAAG[-/AAAAAGAAAC]AAAAAGACAGGGTCT	51317
rs550272279	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930914	TCACAGGCCCCCCCC[A/C]CTCCCCGCCCAGGTC	51317
rs550278168	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038679	TGAGGACTCTCTGCA[A/G]AGTCCCAAGGCAGCA	51317
rs550281104	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984587	CAACAGAAAATCAGG[G/T]TCGTTTTTCCACCGT	51317
rs550281826	snp	A/C/G	0.000181319	0.00951998	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938211	AATTGTTTTCAGAGG[A/C/G]GGGTCTAAGCAGTCC	51317
rs550287925	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45999089	GCCTCAGCCTCCCAA[A/G]GTGCTGGGATTACAG	51317
rs550291668	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098219	TGTACATAAATAAAT[C/G]GAAGTAATAAAAATC	51317
rs550340067	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45993900	TATCTGAGATGAATT[C/T]CCTAGAAACTGCTCT	51317
rs550341338	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009554	CACAGTTCTAAGCAC[A/G]CTATGTATTACATAA	51317
rs550358742	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958520	AGTCCCAGCTACTTG[G/T]GAAGCTGAGGCGGGA	51317
rs550378146	snp	G/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46016734	AGACTAGGTCTTGCT[G/T]ATTTTATAGCCCACT	51317
rs550396867	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021678	TCTCAAGTCTCTGAG[A/C]CTATAGGCACACACC	51317
rs550421924	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957869	AAAAGAATAACAAAA[C/T]CGACAAACCTCTGGC	51317
rs550463406	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945253	GAATTCTGAGCTTTG[C/T]TGAGGTTCATTTAAA	51317
rs550464026	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001874	AACCCAGATGGGCCA[C/T]AATACAAGATACTTA	51317
rs550473142	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46095723	ATCTGAAACCCTTGC[A/G]ATATGAAGAATCTGT	51317
rs550490276	in-del	-/AAT			intron-variant	PHF21A	GRCh38.p7	11:46028433	TACTTTCATAATTAG[-/AAT]AATAATTATACAATC	51317
rs550520708	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46062432	ATTGAGAAACAACTC[C/T]AATTTTGTTTTCCAA	51317
rs550558421	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46103062	CACAGGAGCACCACC[A/G]GCTGGACAGGGTCCT	51317
rs550588941	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937529	CTTGTCACCCAGGCT[A/G]GAGTGCAGTGGTGTG	51317
rs550609853	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46090099	ATTATCCCAACCACA[C/T]CCAACAAAAGGAAAA	51317
rs550643463	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45949363	GCTCATAAATAAAAC[C/T]GGAACATGAGGGAAG	51317
rs550662994	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45981694	AGAAAAAGAAGTGAA[C/T]GAAGAGCTTTAAATA	51317
rs550704900	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45941328	TGGTAAAAACTTTCA[A/G]TTCTGAATTACAGAA	51317
rs550705827	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970304	ATGGCTTTATTCCTA[C/T]AGAAAATTTTCTAAC	51317
rs550725493	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45980481	AGTACTCAGAACTGT[A/G]ATTGGCACATTGTTG	51317
rs550739688	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990450	TTTTTAGTAGAGACA[C/T]GGTTTCGCCATGTTG	51317
rs550742925	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45996201	CTCCTGGCTCGGCCT[C/T]CCAAAGTGAGCCACC	51317
rs550746594	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028494	CCCTCCTGAAACTCT[A/G]AGACTTCCTGATTCT	51317
rs550750805	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071490	CACATTATTAAAGTG[A/T]AAGTTACTTCATCAA	51317
rs550752377	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45954060	GGAGTGCAATGGCAT[C/G]ATCTCAGTTCACTGC	51317
rs550775759	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45951247	TCAATTGTAAAAGAC[A/C]TACTCCTGTAGAGTT	51317
rs550784663	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45990394	TCCCCAAGGAGCTGG[C/G]ACTACACGAATGCAC	51317
rs550787812	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46112835	CAATGAATGATGCCA[C/T]AATTATAAAGAGACC	51317
rs550812408	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45983088	AAGCAGGAGCAAGGG[A/G]TGCGGGCTAGAGTAC	51317
rs550815548	snp	C/T	0.000537463	0.0163842	intron-variant	PHF21A	GRCh38.p7	11:45953518	CTGCCTTTGGAAACA[C/T]AGGCCTACCTGAGGG	51317
rs550821516	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998713	GACGGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT	51317
rs550827617	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46060733	GACCTTTGTCAGATG[C/T]ACAGTTTGCAAACAT	51317
rs550868343	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46106323	CAAAAGGGTGGGGGG[A/G]AACCATCAGCTTAAA	51317
rs550880721	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46063172	GGTGTTCAAAATGAA[C/T]TGAATTCGCCGGGGG	51317
rs550883388	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46104088	TAAGAAAACATCAGG[C/T]ACCAAATGAGAGGAA	51317
rs550906363	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987761	TAAATTAAGCTCCAA[C/T]AGAGCAAAACGTCTG	51317
rs550915457	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029275	ATACTTGTTGAATTT[C/T]TCCTCACATAATAGG	51317
rs550961345	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978349	AAAACAGAGATGGTA[A/G]TAATAATAACTTCCT	51317
rs550973875	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46063117	TGGGGAGAGGAATAG[A/G]GACGAAGAGAATAAA	51317
rs550974029	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054153	TAAAATACACTAGTA[A/G]AAGTTGTATTCCTCT	51317
rs550979210	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46051228	TACTAGATCTAATCA[C/T]TGCTGCTTTAAAGAG	51317
rs551008579	snp	G/T			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122258	AGCGAGGAGAAGTGA[G/T]GGGGAAGCACTGCAA	51317
rs551022875	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941471	TAAACCCCACTGTTC[A/G]GTCTTGAGAGAATGA	51317
rs551030941	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097710	AACCATCCTAATTCC[C/T]AATTCTTCCTTTGTT	51317
rs551050023	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080351	TTTTGTAGAGACAGG[G/T]TCTTGTTATGTTGCC	51317
rs551053607	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45937388	TAATATGTTTGCCTT[C/T]TAAGTCTATAAAATA	51317
rs551078832	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45962446	AGAAAACAAGGATAG[G/T]TGAAAGATACGAAGT	51317
rs551084253	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45964026	AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT	51317
rs551097868	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45971510	CTGTAGAACAACATT[A/T]CTTTTGTGTACATAC	51317
rs551136089	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46079547	CCCACACAAAACCGG[C/T]CTGTTCATACACAGA	51317
rs551172943	snp	A/T	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:46007309	TCCATCTACCTTTTT[A/T]CTTCTTCTTCTTTTT	51317
rs551221238	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097040	CCAACCATGTGCCTC[C/T]ACCTTCAAAATATAT	51317
rs551228687	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988516	AAGTACATTCTTAAT[A/G]TCACACTCTTGATGC	51317
rs551236436	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46026727	AAAAAACCTGAGACA[C/T]GTTGGCTTGGCAATC	51317
rs551247400	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952416	CTGGCTAATTTTGTT[G/T]ATTTTTTGCAGAAAC	51317
rs551256195	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104827	GTATGCAGCACGTAT[A/G]TGATACATCTTTATT	51317
rs551281485	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045271	TACCATGTGTGTTTA[C/T]TTCTTTTTCCCTATG	51317
rs551302293	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070586	TCTGCCTACCTTGGC[C/T]TACCAAAATGCTGGG	51317
rs551304116	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928917	CCTCCGCCATCCCTG[C/T]TATTTAAATTATTTA	51317
rs551310569	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961739	TAAACATTAAATACC[C/T]GACTTCATTTCATCA	51317
rs551315578	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46036883	TATGTTTAAAAAAAA[A/T]TTTTTTTGTAGAGAT	51317
rs551328223	in-del	-/TCA	0.00119737	0.0244387	downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929162	CAGTGCACAAGGGAG[-/TCA]GTGCTACATCCAGCT	51317
rs551353552	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46052197	AAACAAATAAAAAAA[A/T]CTTTCCCTCTTCAAT	51317
rs551354775	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46048688	GGCAGGAGAATCGCT[A/T]GAACCCGGGAGGCAG	51317
rs551372635	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944989	GCTGGTCTTGAACTC[C/T]TGACTTCAGATGATC	51317
rs551373450	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45997880	CCTAAAACTACCACT[A/T]CAATCAACTCGAGTC	51317
rs551391523	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46044611	ATTTTGCTTCTGCAA[C/T]GGTTATCCAAACTCT	51317
rs551401759	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036144	TGATGACTGAATTTC[A/G]GAGATGAGTGAAAGG	51317
rs551415488	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45951056	ACTGGGCCCTGAAGA[C/T]GGAACGTTAAGACTC	51317
rs551534958	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004129	TGAATAAAATCCTGT[C/T]TCCCCTTTTTCTTAT	51317
rs551537540	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46078863	TAAGCTATATGACAA[A/G]TATTAACTCAATATT	51317
rs551542027	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46021191	CAGCTTCCAGAGCAG[C/G]TGGAACTACAGGTGC	51317
rs551550358	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46089860	CTACACAGGTCATAC[C/T]TCCACTGCAACGTGC	51317
rs551555278	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46080076	CTAATGGAAAAATTT[C/G]TCACTCTCTTTTGGT	51317
rs551562703	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45962298	GAGAACGTTGGATAC[A/G]GGTTTGGTAACTGTG	51317
rs551568347	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46079492	CTTTCAAATGTTGTC[A/G]ATGTCTAGAGTCCCA	51317
rs551575121	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46017583	TTGCCCTTAAGGGGG[-/A]AAAAAAAAAAACACC	51317
rs551579880	snp	C/T	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120710	GAACACCCCCCTTTC[C/T]CTCCTCCCTCCCACA	51317
rs551591553	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46113637	GATCGAGACCATCCT[A/G]GCCAACATGGTGAAA	51317
rs551599345	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122582	TTGTGTAGCAGGGCA[A/G]TCACTGGGAATCGGC	51317
rs551609107	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995973	ATTTAGACACAGGGT[C/T]TCCACTGTCACCCAG	51317
rs551609384	snp	C/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085675	CACTACTCCTTAAAC[C/G]AATACAATAAGATTC	51317
rs551614517	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46014706	TATTCTGGGGCCGGG[C/T]GCGGTGGCTCACGCC	51317
rs551624067	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46091958	TTTTAACAGGTTATC[A/G]AACGGTGGAACATGC	51317
rs551650500	snp	A/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45953244	ATCGCTCATCTTAAC[A/T]TTTCAAATTTGTAAC	51317
rs551664970	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006322	GAGAAATCAGTAAAT[G/T]CTTAATCTTTCGGTT	51317
rs551674537	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112017	TTCTAACAGTGCAAA[C/T]ATTGTAAACAATAAA	51317
rs551707889	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032418	ACGAATACATTTCCA[C/T]GTGAAAATCAGTATC	51317
rs551757168	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45987427	GGCACTTTGGGAGGC[C/T]GAGGTGGGCGAATCA	51317
rs551766309	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987527	TTAGCTGGGCATAGT[C/G]GTGGGCGCCTGTAAT	51317
rs551777970	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46096015	CCACTGGCTTTACTG[C/T]TTTTTATCTACCCTT	51317
rs551779709	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46086942	AGAAATAAGAATGAC[C/T]AACAAACATGAAAAA	51317
rs551784403	snp	C/T	0.00358891	0.0422285	intron-variant	PHF21A	GRCh38.p7	11:46029138	ATTAAGGGCTTAACT[C/T]AAGAAGTCAACGATA	51317
rs551784781	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46083124	AGACGAGCTTGTTTT[G/T]GTAACAAATTTCTGC	51317
rs551791257	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044265	TTTTGGCTTTATTGA[G/T]AATACATTATTAAAC	51317
rs551793480	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46103164	GATTTTCAAAATTGT[A/G]TAATTCTTTAACTCA	51317
rs551803028	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46031827	ATCTGTAAGTACTCA[A/G]GGGTGACATTCACTC	51317
rs551818516	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46038253	TGCCTCAGCCTCCTG[A/G]GTAGCTGAGATTATA	51317
rs551899898	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45978229	TGTTTGAACCCAAGA[C/T]GGTGGAGGTTGCAGT	51317
rs551919876	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46068192	GTCACATGGAAGTAA[C/T]ACTGCCAAGATTTTC	51317
rs551924021	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041375	ATTTGGGCACTGTGC[A/G]TACTTCTTTCGAGCA	51317
rs551932981	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45999897	GGCATAGCAGTGGTG[A/G]ACAGGAAGGCTTGTC	51317
rs551934889	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45967094	CCTTTCCTGGCCGGG[A/C]ACAGTGGCTCACACC	51317
rs551946065	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087785	TCCTGAGATAGGGTC[C/T]TACTGTGTCACCCAG	51317
rs551946926	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45982414	AATGATGCAGAGTTT[A/G]AAGTCTTTGCAGAAA	51317
rs551965381	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45951316	TTATCCTCGATATTA[C/T]CCTACTTTGGCCTGA	51317
rs551971925	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45964070	GGCATGGTGGCTGAC[A/G]CCTGTAATCCCAGCT	51317
rs551979736	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111427	GTGAGCTGATATTGC[A/G]CCACTGCACTCCATA	51317
rs552000619	in-del	-/A	0.00953873	0.0683987	intron-variant	PHF21A	GRCh38.p7	11:46055117	CCATTTTGGACTTTT[-/A]AATTATGGCGAGAAC	51317
rs552006794	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992161	GATAAAGCCCATGGG[C/T]CACCAGTTTTCAACC	51317
rs552015506	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46060418	AAAAAAGGCAAGAAA[A/C]AAGTTGTAATCTTAG	51317
rs552020299	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104028	TCTAGGCTCAACATA[C/G]GTAGCTTATGACAAT	51317
rs552036717	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052946	ATGCAGATACACATG[C/T]GCTACAAGATGAAGT	51317
rs552057136	snp	A/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46112756	CAACTATCCCCATTT[A/T]AAAAAAAAAGGAACA	51317
rs552058237	in-del	-/G	0.0103295	0.0711199	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120359	CCGAGGGACAGCCGA[-/G]GGGGGGGCGGGCGAG	51317
rs552068707	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094925	AATCATGAAATCCTT[C/T]AAACCTAAGGGATCC	51317
rs552093272	snp	C/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934799	TCAGCCGGGGACTTA[C/G]AGTCTTTTGCCCTTT	51317
rs552120250	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45947676	TTAACCCCTGTCCTC[C/T]TAGCAGATACTGCCC	51317
rs552214656	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46057212	ACTTGTTTATTTTCC[A/G]TCTTGGAACTACATA	51317
rs552248135	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932598	TTAATAGAAATCACT[C/G]TTTTTAGGAAACAAA	51317
rs552272877	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46103660	ATAGGAGCCATTATG[C/T]TACTTTAACTTAAAT	51317
rs552273743	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46081388	TAGCCACAGTCTTCA[A/G]TGAAAAAAGCTCTTG	51317
rs552286140	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46077431	TAGATGAGATACACA[A/G]AGCATGATTGCCTTT	51317
rs552286874	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966605	TAATAGCCAGTTTTT[G/T]TTTTTTTGTTTGTTG	51317
rs552323826	snp	A/C	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46048625	AAATACAAAAATTAG[A/C]CGGGCATGGTGGCAT	51317
rs552328357	snp	C/T	0.00993419	0.0697739	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930470	ACCAGCAGGCTTACC[C/T]CAAAGGGCCTGATAA	51317
rs552333080	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46089305	TAATATGTAGGTAGA[C/T]AAAATAATATCTTTA	51317
rs552340176	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46108086	AAAATCCTACTTTTT[A/G]TTTTTTCTTTTTTAC	51317
rs552344138	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46084070	AAATTGTCTTAAAGA[G/T]TATTAAAAACTATAC	51317
rs552359025	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008527	ATGGGTCAAAGGTAG[A/G]AGACGGGAAAAGAGT	51317
rs552372319	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939175	GAGAGGTCTATAGTC[A/G]CCAAGGCCAAAATTA	51317
rs552384473	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930352	CAGCAGGGACAGAGA[A/G]GCAGGTGTTGCAGGG	51317
rs552419348	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45982804	AAAACCCAAAACAGA[C/T]CAAATCAGAAGAAGG	51317
rs552436316	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938420	GACAATCAGCTGCCT[C/T]GTTCCAGGAGTACTC	51317
rs552441102	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039210	GAATACTAATGAAAC[A/G]TTTAAAAAGTTATCT	51317
rs552448470	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100083	CTTTTGAAACAAAAA[C/G]CACAAAGAAACAGGA	51317
rs552463444	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091321	ATTTTTTTCATAATA[C/T]ACACTCTCCTAATAA	51317
rs552495059	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46090021	CCTGGGGTCCAGGCT[A/G]TCTGAATATACACAT	51317
rs552499264	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45972444	CTGTATATTTGCACT[A/G]TCTGATTTGGCAGCC	51317
rs552504141	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955567	GCAATTAGCAGCAGT[A/G]CTTTTAAGGAAGGGC	51317
rs552536467	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014709	TCTGGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	51317
rs552555750	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46073144	CCATCCTGGCTAACA[C/T]GATGAAACCCGGTCT	51317
rs552595322	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46022456	GAGACCCTGTCTCTT[-/A]AAAAAAAAAGAAAAA	51317
rs552610119	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073234	TTGGGAGGCTGAAGT[A/G]GGAGAATGGCGTGAA	51317
rs552621560	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45990128	CTACACAAATATTTA[C/T]AGTCTTCACACCTGA	51317
rs552630673	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46057980	TGGAAATTCAAAACA[C/T]ACCTGTTTTCCTACT	51317
rs552633228	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080670	CTACTATTCTTTTTT[C/T]GTTTTTTGTTTTTTA	51317
rs552643309	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45981487	GGGACCAAAGACCAA[C/T]AAATGGCTCATAAAG	51317
rs552674201	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45978017	TAAAAAACAGAGATG[G/T]TGGGCCGGTTGCGGT	51317
rs552692968	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46055854	ATTATTTTACTTGGA[A/G]TTAAAAGGATATGGC	51317
rs552714329	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038343	ATGTTGGCCAGGCTG[C/G]TTTTGAACTCCTGAC	51317
rs552756501	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030195	GGTTTAGAATCCCAG[C/T]CTCTGAAAAGAGCTT	51317
rs552757996	snp	G/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45964981	TTATTGGGCCGAAAC[G/T]AACATGGCGTTTTCT	51317
rs552788069	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46081483	AAAGGTTTTCTTCCA[C/G]ACACTGGAATTTAAA	51317
rs552828216	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038763	CTCTTCCTTTTCTTA[A/T]AAAACCACTAGTTCC	51317
rs552839815	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46081821	GCCATACTCATTCAT[G/T]TATATATTGTCCGTG	51317
rs552849806	in-del	-/T	0.0152052	0.0858568	intron-variant	PHF21A	GRCh38.p7	11:45999860	TATATAGAAACATCG[-/T]TAACTTTTCTCTTGA	51317
rs552884122	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46013359	CTTAGTAGCTATCTC[A/G]GTTATCAGATCAACT	51317
rs552888564	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929732	GAGCCCTGCTTCCGT[G/T]TAGAGGAGGTATTTT	51317
rs552889603	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022314	TTAAAAATTAGCCAG[C/G]TATGGTGGCTCACAC	51317
rs552917972	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022133	TAGAACAAAACCATG[C/T]ACTGTTTGTTTCTTT	51317
rs552923537	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45960047	GGTGTGGTAAGGATG[A/C]GGAGACAATGGAATG	51317
rs552939373	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013586	CACAGTCATGTGTTG[C/T]TTAATAACAGGGATA	51317
rs552976244	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46012958	TAGGGGAAAATTTAC[C/T]ATCAGTCCCCCTTAT	51317
rs552982546	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930674	CCAGTCATCACTGCC[A/G]CCAGGGCGCAGCGCC	51317
rs552993395	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972660	GGCTCGTGCCTGTAA[G/T]CCCAGCACTTTGGGA	51317
rs553047910	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113471	AAAAAATATAATTTT[C/T]GAAATAGTTTTTTAA	51317
rs553051882	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006500	ACGCTATATAAATAA[A/C]AAGGAGTCTAAAAGT	51317
rs553059424	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963918	ATAATTTATTTCTGG[A/G]CTGGGCGTGGTGGCT	51317
rs553087731	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929983	CTCAACAGAAGCCAC[A/G]GGATCTGGAGAACCC	51317
rs553108324	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45988784	TAGTCCCAGCTACTC[A/G]GGAAGCTGAGGCATG	51317
rs553113727	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062066	CATCTGATTCCCAAT[A/C]CCTGTTTGCAACTGT	51317
rs553149528	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45936743	AAAGTTCCAAATATC[A/G]GCTTAGGAGAATCAA	51317
rs553172851	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935857	AGCTCCCATGAGTCC[C/T]ACAACCCAGTGCAGA	51317
rs553193048	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45996905	TGACTACTAACTTAC[C/T]TTCTTTGGGCACAAA	51317
rs553197446	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978450	TATTAAATGTTAACT[C/T]ATCTTTAGTGTTCTT	51317
rs553199680	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46106448	GTCCTGATAAGTTAA[C/T]GGCATCTGTTCCTTT	51317
rs553202619	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45957394	TTAGGCCACAAAACA[A/C]ATATTAATAAATTTA	51317
rs553227807	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053535	GTTTTTCTTCATTAT[A/C]TATATAATTATATGT	51317
rs553234405	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105409	GATTAGATCACTGCA[C/T]GACTCAGGAAGTAGC	51317
rs553246474	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019698	AGCAATGAAATTTAG[C/T]CGTATTAGTCTCCGG	51317
rs553279118	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45969497	AATAAGAAGTGTTAA[C/T]TGCATTCTTTCCCCA	51317
rs553312183	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098330	GCATATTAACTTCTA[C/T]ATGCTTGAAAAATGT	51317
rs553334334	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46027711	TATGAGAAGACGCCT[A/G]TTGTTCCCATATGGA	51317
rs553339967	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46010509	GCCTGAATTTCTTTC[C/T]GCTTTACGACATTGT	51317
rs553340996	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45979591	TATTTCCTTCTGCCA[A/G]TGATTACAAGTGATA	51317
rs553343990	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001580	TAACACTGAATTTTT[A/G]TATAAGAAAAGAACA	51317
rs553348002	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45934463	AACAGAGGGAGAAAG[A/G]GCATGCGGGCACCAA	51317
rs553381014	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009699	AGAGCCAGAGCAGAC[G/T]TCCAACTTGGGCAGT	51317
rs553385072	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931700	TCCTAGACTCTGGCC[A/G]TTCCCAGGGCCTGGA	51317
rs553387238	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46099905	CTTTAGGCCTAAAAA[C/T]TAAAAATGGTTCCAT	51317
rs553396396	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45998262	CCTTTGAGTCATCCA[C/T]AAATATCAATTTGCC	51317
rs553402505	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45980983	GGCCTTGCTCAAATC[C/G]AAGAGAAATGTGTTT	51317
rs553410385	in-del	-/AGA			intron-variant	PHF21A	GRCh38.p7	11:46118715	TAAACAAGTAAAGAC[-/AGA]AGAAGAGAATAAGAA	51317
rs553426493	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071549	TCTTTGACCAGTTAG[G/T]TATAAGTACTGGCAG	51317
rs553441582	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46015562	ATTTTTAAACTTTTT[G/T]ACTCTTTGTAATAAC	51317
rs553451545	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114252	TCCAAACACAAGCTG[A/G]TAAGTTTGAGCTAGA	51317
rs553485900	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119146	CAGCCCAAATTAATC[A/T]GATTCTAATATTCAA	51317
rs553514936	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088082	TTTGAGGTCTTGGAC[A/C]TCTCATGCAGTCATC	51317
rs553525401	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997859	CAATAGGTCCTCTTA[C/T]CAGAACCTAAAACTA	51317
rs553540514	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46062635	AGCAGCTTCCCTTAA[A/G]TATCTAGTGATTCTT	51317
rs553546923	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944608	TATCCTGGCCCTCTT[C/G]CTTTTCTTTCAGGAT	51317
rs553560689	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966189	TTACCATCTATGTAC[C/T]GAAGACTCACACTTT	51317
rs553562445	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45975002	TCTGCCTGCCAAATA[C/T]GAAGTATTGATTTAA	51317
rs553586099	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46050315	GGGACTAATACCACT[A/G]GGTCTTGTTGAAGAA	51317
rs553589890	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078107	AATCCAATTTAAATT[A/G]TGACTATACCAAAAA	51317
rs553603825	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45946261	GAAGGTGCTGGCTTA[C/T]GTAGAAAGACCTCAC	51317
rs553615290	in-del	-/C	0.0138799	0.0821421	intron-variant	PHF21A	GRCh38.p7	11:46028091	AATCTCTGGGGACAA[-/C]TTTTTTTTTTTTTGA	51317
rs553621651	snp	C/T			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123391	TTAAAAAATAAAATA[C/T]GGACTTTATGGTACA	51317
rs553636315	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024673	AGGTGTGGTGGCACA[C/T]GCCTATAATCCCAGT	51317
rs553643924	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037291	GTGTCACAATCCTGT[A/T]CCCTCAGAATTCTAT	51317
rs553645627	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46020550	TTTTCTGCTTCCCTT[A/G]CGTCTAACACCATCT	51317
rs553664555	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070914	CCTGTGACAGGGTAT[C/T]TCATGGGGAAAATCA	51317
rs553664712	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084422	GGCAAGAAATTTCCC[A/G]AAGAGATTTTTTTTC	51317
rs553682086	snp	A/G	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46109997	AAAAAAAAAAAAAAA[A/G]GTACTGGTCTATTGG	51317
rs553698202	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966746	TGCCCCAGCCTCCTG[A/T]GTAGCTGGGGCTACA	51317
rs553728497	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46072722	TAGCTCCTCTGAGGA[A/C]GTGACATTTAAGCTA	51317
rs553731369	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958901	CCAGTCTGGGTAACA[C/G]AGCAAGACCCTGCCT	51317
rs553739429	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46118179	ATCCATCACTTATAC[C/T]TTCTAAAAATACAAT	51317
rs553743203	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46100180	AGACCTCAAAAAGAA[A/G]TTGTTTGCTTGATAT	51317
rs553752102	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079226	CTCCCTATGGCTAAT[C/G]AGGTTTGGACCAAAA	51317
rs553766926	in-del	-/TCAT			intron-variant	PHF21A	GRCh38.p7	11:46107938	AGGTGATGGGGATGA[-/TCAT]GGTCAGCCCACACTA	51317
rs553767691	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939427	TACAGTGAAAGTTCA[A/T]ATGGGAAAATATTAA	51317
rs553780072	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099595	AACACAAAGGGAATG[A/G]TACTCTTTCACTTGA	51317
rs553816656	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092013	ACAAATGCGTTTGAA[C/G]TATAGCTACGTGAAA	51317
rs553824585	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974263	ACCCCTACTCTGGTG[C/T]TTCTTCTTTCCCAAG	51317
rs553834491	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931971	GAGGCTTGTGGGTGG[G/T]TGGAGTGGAGTAAAT	51317
rs553857851	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049895	AAAGCAACAGAATCA[A/G]GAGATTAAGTACTAA	51317
rs553858682	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46068155	GTGCTAATGAGCTTG[A/C]ATGCCTTGTAGGTCA	51317
rs553860656	in-del	-/T	0.444554	0.156999	intron-variant	PHF21A	GRCh38.p7	11:46110789	CTACATATTAACAAT[-/T]TTTTTTTTTTTTTTG	51317
rs553887964	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016258	TGCTAGTAGAACAAT[A/C]TTTCTCAAAAAGGGA	51317
rs553899161	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933407	TTTGATACACTGTCC[C/G]ACCCCCTGCTCCCTC	51317
rs553923406	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46101713	CACAATCACAGCCTC[A/G]CAGCCTCGACCTACC	51317
rs553946225	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059132	GTATTCCTTATCTGA[C/T]TTTTTTTACTTCTAG	51317
rs553969985	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46064960	AAATAATCCACAGAG[C/G]CAGTAACAAGCACTA	51317
rs553971624	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023917	GCCAAGATCGTGCCA[C/T]TGCACTCCATCCTGG	51317
rs554048459	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032714	TCTATCTCTTACAAG[A/T]ACACAGACTTGATAC	51317
rs554055825	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46105616	CTTCCCAAACACCAT[-/A]AAAAAAAACACAAAA	51317
rs554060493	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067147	CATTTGTTTTCAAAT[G/T]TTCTTTTGTGGGGAT	51317
rs554084303	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45957106	GTTATAATCATATAT[A/G]TACCAGACAACAGAG	51317
rs554085869	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946872	TCAAGTTAACTATTC[C/T]TATCCCTTGCTTTTA	51317
rs554097720	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46014991	TCTCAAAAAAAAAAA[A/T]AAATAAAAATAAAAA	51317
rs554104468	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016883	AATGATCAAAATTTG[G/T]ATCAGCAATTCTGGG	51317
rs554143109	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45937534	CACCCAGGCTGGAGT[A/G]CAGTGGTGTGACCTC	51317
rs554145714	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45972988	GAGGCTGAGGCAGGG[A/G]AATCACTTGAACCCG	51317
rs554155744	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931246	TAGTGATGATGGTTT[C/T]CCAACTTCTTTCAGG	51317
rs554174618	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040866	TATAAATCTATTTCA[C/T]CCTTAGAACTACACT	51317
rs554180139	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45962332	AGGTGTGAACAGGTT[C/T]TTCCATGGCTACATA	51317
rs554180718	in-del	-/AT	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46034318	AACCCTTTGTCACAC[-/AT]GTGTTAAAAATATCT	51317
rs554192181	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015872	CCTGAAGGACCTGCC[C/T]GAGGCTATTGCTGTT	51317
rs554201694	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46117075	CAGAAGCTTCTGTCC[A/C]TGTATTAATTAGTTA	51317
rs554252702	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46063017	CTTGATCGTGATGAC[A/G]GTTTCACACCATCAA	51317
rs554267616	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46009618	CTATATAGTATGCTA[C/T]TTTACAGATGGAGAA	51317
rs554296683	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46105361	AGCATGTGTGCCAGA[C/T]GTCTTTACAGGCACA	51317
rs554296839	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116311	ACACATACAGATATA[C/T]ATCTTTTTCACTGTG	51317
rs554340755	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45996280	TTAAAAACATAGGAT[C/G]TAGTACTCAAGGTAG	51317
rs554363221	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058102	AGGATCTCACTTAAA[C/T]CTGCAGAAAACAGAA	51317
rs554395406	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007864	TTTTCCATCTTACTC[C/T]TAAGTGGAATGTCAG	51317
rs554397990	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46117835	ATCCTTATACTATCC[A/G]CAATCGCACATCTAC	51317
rs554398347	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067051	TCCATAATATGCATA[C/T]ATAGCTAATGTATTC	51317
rs554400028	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46042675	AACTGTATTATGAGG[C/T]GAGGTCTTTAAGAGG	51317
rs554409610	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45990866	ACATTTGTTACAATC[C/G]AACCTACACTGACAC	51317
rs554453461	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091454	TTAGGAAAAAATGTT[C/T]GCCTGTATGCCCCAC	51317
rs554464432	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107584	CGTGGATCTAAAGAA[A/G]CATAAAGCACCTTAG	51317
rs554469033	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46000140	CACAATAGTACCAGT[C/T]AAATTGTTAGTGAAG	51317
rs554485079	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46056112	CTCTGTTTCCTATCT[C/T]AAAGTAACAAAATAC	51317
rs554508062	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45999441	CCAGTGAAATAGCAC[A/G]TAGTATATACTTCCA	51317
rs554512135	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46065756	TGTTTAAGCGCCACT[A/G]TGTGTGAAGCACTAG	51317
rs554535203	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966079	TCTGCCTCATCCTAA[A/G]TGTGAGTATTTCTTA	51317
rs554539914	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45989942	GGCTGCAGTGAGCCA[C/T]GATCGTGCCACTGCA	51317
rs554542336	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46117291	GCAACCACAGTGGCA[C/T]GATATTTTCAGTGAT	51317
rs554551545	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023889	TGAACCCAGGAGGCG[A/G]AGGTTGCAGTGAGCC	51317
rs554570837	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46065958	CATGAGATGTTAGGG[A/C]GGGCACATCCAAGAG	51317
rs554578381	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116083	GCTCATAAACACAGG[C/G]TTCCTAATTATCTAT	51317
rs554596559	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974151	GTTTGTCTAGTATAC[A/G]GGCACAAGACCTAGT	51317
rs554597057	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45982176	TGCCCAGGCTGGTCT[C/T]AAACTCCTGAGCTCA	51317
rs554624131	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45939734	CACCATCAGAATAAA[A/G]CAGATCTACTTAAAA	51317
rs554653983	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45990840	ACTATCAACAAGCTA[A/C]ACATAGCAGAACATT	51317
rs554658924	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45992282	TCATGCTTGTAATCC[A/T]AGCACTTTGGGAGGC	51317
rs554661493	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45986853	TCACTTGATTTTTAA[C/T]ATCTAATCATTTTAA	51317
rs554673498	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055905	GCTAATTCAGAATCA[C/G]TTCCCATTTGGCAGG	51317
rs554674878	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46000442	GCGATATGGGACTAA[A/G]GACAAGTACACAATT	51317
rs554682083	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45949097	CTCAAGGGTTTTATT[G/T]TATGTACTTGGCTCT	51317
rs554683067	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057154	AAACTAAGAGCAGAA[C/G]AGTTTTTACTGGGTC	51317
rs554702226	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46007733	TTTAAATCAAAAAAC[A/G]ATGTGAAAGAAGTGA	51317
rs554720300	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023094	GCTAAGGTCTCAGAC[C/G]TTGAGTGATATGTGG	51317
rs554746351	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45953910	TTTAATTCCTAAGTA[C/T]AGAAATACGGTACAG	51317
rs554746483	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46066515	CCAGCCTGGGCAACA[A/G]AATGAGAACCTGTTT	51317
rs554747761	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958016	ACAAACTAGACAACA[C/T]AGATGCAATGGAAAA	51317
rs554755163	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931134	GGTCAGAATGTACCC[C/G]ACACTGCTGAGGGCG	51317
rs554764382	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46072643	ACTATGAAGGAAAAG[A/T]ATGGTTCAATGTGAG	51317
rs554786390	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46082308	GGCTTTTGTCCCACT[A/G]TTTCGTCAAATGTAT	51317
rs554860276	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074149	AGTTGTCAGATGCAA[C/T]TTTTTTTAATAAAAC	51317
rs554877720	snp	A/G	6.87151e-05	0.00586113	intron-variant	PHF21A	GRCh38.p7	11:45965273	GCCATATGCCTCAAC[A/G]ACAAGGCTACTGCCC	51317
rs554947121	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46083484	TACTTATCCTTCTCT[C/T]CGCTCCCATATCCCC	51317
rs554954795	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45943372	TTTGTAGAGACAGGG[G/T]TCTTGCCATGTTGTC	51317
rs554971045	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46047761	GTCACTTTTTCTTTG[G/T]GTCAATTTCATCTGC	51317
rs554982954	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998902	ATCTCAGCTCACTGC[A/G]GCCTCTGACTCTTGG	51317
rs555001387	snp	C/T	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:46009135	GTGCATCACCATGCC[C/T]AGCTAATTTTCTGTA	51317
rs555009601	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46046685	AATAATATTAAATGA[C/T]GATGGCAGCGGTGAA	51317
rs555039000	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025237	CAGAGTATGATTTCA[C/T]ACCACAGATACAAAG	51317
rs555056435	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099441	CTTATTGTGTTCCAT[A/C]CTGCCTCACTTCTCA	51317
rs555082497	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45934405	CACCTAAGGAACAGG[A/G]CGGGTGGAGTGGGTA	51317
rs555095646	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040134	ACTAGATGTGGTTTC[C/T]TCTGAACAACCTCTG	51317
rs555105038	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994631	CAGCCTCACCAAGAG[G/T]GGTTATGTTTTAGGC	51317
rs555109078	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46081104	TCCTTTAGTAAAATG[C/T]ATAATCTTTGGTGTA	51317
rs555162362	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46111234	AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA	51317
rs555178681	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46095139	ATCAGAAATCCCAAA[C/G]TGTTTCTTCTGAAGA	51317
rs555191300	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46026706	TGGGCTTTTAAATCC[A/G]TAATTAAAAAACCTG	51317
rs555199778	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45959092	TTATCCCAAGAGTGG[A/G]AGGGTGGTTCAATGT	51317
rs555218712	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45942500	GACAATCTTTGGCGC[C/T]AGCAAACAAGATTTC	51317
rs555221892	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946356	GATGTCAAAGCCCAG[C/T]GGGAGCCAGGGCCAG	51317
rs555240873	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46065289	AAAGTCTGTTGAAAG[C/G]CTTCTAATTAAAGTT	51317
rs555251011	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013715	GCTATATGGTAATAG[C/T]CTATTGCTTATGGGC	51317
rs555266199	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120043	GTGCAGGCAGACTCT[C/T]CGGAATAACAAGTTG	51317
rs555295227	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934957	TGCCACCAAGTACAA[C/G]GCACCACCTGGTATC	51317
rs555316330	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46097193	AAGGTATATTCTCTC[A/G]CAAGCCAGAGTAAGC	51317
rs555319155	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013477	GGGCCTCAGCTGACC[A/G]TGAGTAACTAAAGCC	51317
rs555342433	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995448	TCACAGCATGTTTGT[G/T]TGACAGTTATACTGT	51317
rs555350681	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052300	AAGCAAATGAAGCCA[A/G]AAGAGGGAGAAAGTG	51317
rs555398482	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46003220	GAGTGCCACTAAAAA[A/C]AGTCCTAAAAACTTT	51317
rs555403272	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068221	TCATTCTCTGCATCC[C/T]CCATGGGCCTAGTAT	51317
rs555403395	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46076581	ACTCTAGAGACTGAT[C/T]TCAACCAAAAATAAA	51317
rs555406257	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043465	AAAGCAAACAGAATG[C/G]CAAGTAAAGCCCATA	51317
rs555407126	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059796	CAGTGGCTCAATCTC[A/G]GCTCACTGCAACTTC	51317
rs555419669	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46072426	TATTTTGGACTATGA[C/T]GTGAAAGCTGCATGC	51317
rs555429518	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025676	GAAAATTCCTATATA[C/T]CTTTCACCCAAATTC	51317
rs555508162	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46041797	CTGAACTATCACACA[G/T]CTTTCTTCTCCCATG	51317
rs555510165	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050282	CAGTGTCCTTGCTCA[C/T]GGCAGGAGAAAGGCA	51317
rs555521298	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46034262	GGGAGGCTCATACTT[C/T]TCTTAGAGATTCATA	51317
rs555525291	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46037001	TAGGCAAAAGCCACT[A/G]CACCTGGCCAGTATT	51317
rs555529639	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46093728	GTTTGTTAAGTCAAT[A/G]AATTGACTAAACAGA	51317
rs555544100	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960132	TGGCAGTTCTTCAAA[C/T]AGTTGAGCAGAATTA	51317
rs555561157	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011314	CCCAACATGGTAAAA[A/C]CCTGTCTCTACTAAA	51317
rs555602022	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977467	AACATAAAATGTTAC[C/T]TGAACAGGATGTTTC	51317
rs555606964	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45967668	GACAAATGTCTGATG[C/T]TATCTTGCTCACAAG	51317
rs555620822	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042496	ATGGTTTTTATAAAT[C/T]CTAGAAAACCGAAGA	51317
rs555628581	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010579	TTTGGCACCGGAGTA[C/T]GCTTTTTGGGTTCTC	51317
rs555631576	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933239	GAGATGCGCGACTCA[C/G]CAAGCAGGGAAGGAA	51317
rs555647141	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018677	GCAAAAGATAATTTG[G/T]TAAACATGAACAAAA	51317
rs555664938	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46121395	CTTCATCCTCCTCCT[C/T]CTCTCAGCAGCAGCA	51317
rs555683239	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46046694	AAATGATGATGGCAG[C/T]GGTGAAGATCTAGGT	51317
rs555698425	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45940353	GGCGCCCACCACCAC[A/G]CCTGACTAACTTTTA	51317
rs555754068	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46093135	TAATCAGTGATGAAG[C/T]CAGAAAGAAAATTTA	51317
rs555754158	snp	A/G	0.00795532	0.062565	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119960	CCCGGCCCGCTCGGG[A/G]TCCCGGGGGCGCCCC	51317
rs555774999	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110941	CAGGCACCTGCCACC[A/G]CGCCCAGCTAATTTT	51317
rs555809684	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45985896	GTTGTCATGGAATTT[A/G]TATAGTACAAATAAA	51317
rs555814749	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46033391	CACCTCAGCCTCCCA[A/C]ACAGCTGGGACCACA	51317
rs555839553	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46037802	GCAACAGTATGAATC[-/T]TTTTTTTCCTCCAAA	51317
rs555846027	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026701	TCCTGTGGGCTTTTA[A/G]ATCCGTAATTAAAAA	51317
rs555846484	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994456	CCTCCCTGCTTTCAG[A/T]GCTGCTACTAGGAAT	51317
rs555847652	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46107822	AAATATAATGCCAGA[A/T]AAAATGAACAGCACT	51317
rs555941660	in-del	-/CTCA	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46080858	TTTAAGAGATGAGGT[-/CTCA]CTATGTTATCCAGGC	51317
rs555948787	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958243	CTCTTAAATCATTCT[A/G]TGAGGCCAGCACTAC	51317
rs555957808	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094475	TCCACTAGACCTCAC[C/T]TTCTCTTAACCCGCT	51317
rs555992072	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46110810	TTTTTTTTTGAGACA[A/G]AGTCTTGCTCTGTCT	51317
rs555996158	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45939170	TACAGGAGAGGTCTA[C/T]AGTCGCCAAGGCCAA	51317
rs555996778	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102448	TAATAAGGCATCAGT[C/G]GTATTCTGTATTTAC	51317
rs556014014	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46012831	GATACCCTAAGAGCT[C/G]ATGCTGGGATTTCTA	51317
rs556029001	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46109809	CAACATGGTGAAACC[A/G]TCTCTACTGAAAATA	51317
rs556033432	snp	A/G	4.94181e-05	0.00497057	intron-variant	PHF21A	GRCh38.p7	11:45949390	GAAGGGCCAGATGCT[A/G]GCCAGTAATACCTCT	51317
rs556035965	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45993178	CATGTTATAAACATA[C/T]GACTATTTAATAATT	51317
rs556043991	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45944688	GGCAGGCTCTTCCCC[C/G]AGATCCTCCCGAGGC	51317
rs556049181	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45975275	ACCGTAATTGCACCA[C/T]TGCACTCCAGCCTAG	51317
rs556084802	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959129	ATCAATATAATATAC[C/T]ACATTAACAGAACCA	51317
rs556087396	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45942106	CTGCCACTACTGGGA[C/T]ACTGTAAAAGGAGAA	51317
rs556099891	in-del	-/A	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46113419	GTAGGAGAAGCACAG[-/A]AAAAAAATGCTGAAA	51317
rs556116360	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097978	CTTATTTAGAACCCA[C/T]AGATCTGTATTTAAG	51317
rs556136651	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45938392	ACATTCTAGATGCAT[A/G]TAAATGTTTTAGGAC	51317
rs556145477	in-del	-/ATTAC	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46108047	TCTATTAATTAAAAT[-/ATTAC]ATTACATGTATTATC	51317
rs556157096	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011218	ATGAGGTTGGGCATG[C/G]TGGCTCACACCTGTA	51317
rs556170360	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949550	CTTAACTTCATTGTT[C/T]TATCTATTGGTTTTC	51317
rs556172732	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933223	CAGCGGGATAACCAC[A/G]GAGATGCGCGACTCA	51317
rs556203507	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085200	TAACTGTACTATCCA[C/T]GAACTTATGATGTGG	51317
rs556212649	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46050445	CTTTTGAGAGGCCCA[C/T]GCAGGGAGGCAAATT	51317
rs556226228	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46105153	ATTTGGCCACAGTCA[A/G]AGCTAATACGTGGCA	51317
rs556242304	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092980	AGCTGGTATCAAACC[C/T]CTGGGCTCAAGCAAT	51317
rs556258244	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032919	GTATGTATACATACA[G/T]GTACATATAATCTCT	51317
rs556262714	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46101960	ACTCCTGTGTTCAAG[C/T]GATTCTCCTGCCTCA	51317
rs556278398	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45983676	TAAAGGAGAGTTGCT[C/G]TGCATATTAGCTGGC	51317
rs556291726	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45934383	CCTCAGTGGAGTGGG[C/T]GGCTACCACCTAAGG	51317
rs556294749	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46041729	ATACATAAAAGTTCA[C/T]AGTATAGTGATCCCT	51317
rs556354849	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46057025	GGTTATAGTAAGTGC[C/T]GAAAAAATTAAAATG	51317
rs556355348	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017950	CTAACTAGCTGTAGG[A/G]GTTAAAAAATGTGTC	51317
rs556361914	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46062829	GCATTTACTGAAGAG[A/T]AATGAAAGCAGATCT	51317
rs556396806	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46073085	TGTAATCCCAGCACT[G/T]TGGGAGGCCGAGGTG	51317
rs556430292	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049676	AACACAGCTGCAAGT[A/G]ACAAAGAGCAGCCGC	51317
rs556437922	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932100	AGAGACGTACCCTCA[A/G]AACATGTCACTCCTC	51317
rs556440856	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46017154	TTTTGTATTTTTAGC[A/G]GAGACGGGGTTTCTC	51317
rs556446738	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025605	TCTTATAATCTCATT[A/T]AAAAAATTTTCACTT	51317
rs556466604	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057810	TTTCTAGATGAGAGC[C/T]GACTCAGAGGTGCCA	51317
rs556473028	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048827	TTTCTTTAGGATCTA[C/T]ACCTGGAAATACATA	51317
rs556512833	snp	G/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46008790	AAATGTAAATTCAAC[G/T]GCAAAATGCTATGTT	51317
rs556548685	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46039719	AAAGACAAAAGGTCA[A/G]TATTATAAAGAGCAA	51317
rs556575179	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929897	AGGGTGAGGATGGGA[C/G]TCCTGCTTCCTGCCA	51317
rs556586748	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074977	AAATATAAAAATTGC[A/G]GGACTGGATTTCAGT	51317
rs556592270	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46109591	ATTCCCATGACAACA[C/T]ACCAGTACATTTATA	51317
rs556605270	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46034074	AGAAGTAAAATGATA[C/T]CTCACTGTGGTTTTA	51317
rs556606093	snp	A/G	0.209997	0.246779	intron-variant	PHF21A	GRCh38.p7	11:45962672	CAAGGCAGGTGGGTC[A/G]CCTGAGGTCAGGAGT	51317
rs556607304	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46066488	GAAGGATCACTTGCC[A/T]GGAATTCAAGACCAG	51317
rs556615742	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46089211	CTTGACAGTCATCTA[C/T]GTATCTTTACTTCTT	51317
rs556651918	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46086355	TGATCTCCTGACCTC[A/G]TGATCCGCCCGTCCT	51317
rs556684201	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079967	CGCTGCCCAAAGTTA[A/G]CAATAACCATAGACA	51317
rs556690765	in-del	-/AC	0.326477	0.238015	intron-variant	PHF21A	GRCh38.p7	11:45955298	AACACACACACACAC[-/AC]ACACACACACTTTTT	51317
rs556740899	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071847	ATGTTCTCAAAGAAC[A/G]CTCAAAAATCTAAGA	51317
rs556749336	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972527	TCACACATGTAATCC[A/C]AGCACTTTGGGAAAC	51317
rs556755946	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053412	AATCATAAATGTGCT[A/G]TACTTTCAACCTCCA	51317
rs556763436	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46030347	TCTTTCATAACAAGA[C/T]GATCCTGCACGATCT	51317
rs556772737	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983204	TTCACAACTGCTCCT[C/G]CCCCAGGGCCTGAAA	51317
rs556783409	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45969200	AAGTCAACACTCCTC[A/G]AGGTCCAGAATGGGG	51317
rs556795641	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46117725	ATTACAAATAATTTT[C/T]TAAAATACATGCTCA	51317
rs556808183	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46117152	AGAACTTTTATATGT[A/G]TTATCTCATTTGGTC	51317
rs556811477	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940320	CCTGCCTCAGACTCC[C/T]GAGTAGCTGGGATTA	51317
rs556820965	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:46003297	TCAAAAAAAAAAAAA[-/AA]TGCCAAGTTTTCTTT	51317
rs556826962	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089561	CTACTGCACAAAGAG[C/T]TTGGCAACCCTGATT	51317
rs556831784	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045439	GAAAGAACAGAGAGG[C/T]TGTCTGATCCAGTGG	51317
rs556865081	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45992457	AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCA	51317
rs556868116	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054220	AAAAAAATTTTTTTC[C/T]AAAAGGAAAAGCTGA	51317
rs556869425	in-del	-/A	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46038494	TATTCTAGGTTCTTG[-/A]AGGAGGTAAAGGAGT	51317
rs556870041	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46015474	ATTCTTATAGTTTGA[A/G]ATTTTAAAAATTTAT	51317
rs556875902	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104565	ACACTTTTATCATCT[A/G]TACTCTTTCTCACCA	51317
rs556887422	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46029665	TGCACTAGAGCCTCC[A/G]TCTCAAAAAAAAAAA	51317
rs556923817	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038289	TGTGCCACCACACCC[A/G]GCTAATTTTTGTATT	51317
rs556927476	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45944788	ATCTCTTTTTAGAGA[C/T]GGAGTCTCACTCTTG	51317
rs556931072	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978603	GTGTTGGTTGTAAGA[C/G]GTATCCACGCTTAGG	51317
rs556949842	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46022192	TTGTGGTGGCTCATC[C/T]CTGTAATTCCAGCAC	51317
rs556964179	in-del	-/TGTTTAAAACT			intron-variant	PHF21A	GRCh38.p7	11:45977602	AACCTAACCCAATTC[-/TGTTTAAAACT]TAAACAAAAATTATC	51317
rs556970015	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037591	TCTGTTGCGGTGAGC[C/T]GAGATCGTGCCAGCG	51317
rs556988272	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46061745	AATTATCTAAGTTTT[C/T]CCCTTCATCAAATGG	51317
rs557035460	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011979	GATTTCCAGATGACT[A/C]TCACCTTCTTTACTT	51317
rs557046377	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46008872	CACTCCCATTCCACT[A/C]CTTATTTGACCAGTG	51317
rs557047410	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45971958	TAAGGATTAGCATGT[C/T]GCCTCTGAGGTAGTT	51317
rs557075346	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46021441	CCATCAGTATTGTCA[A/G]TCTAGAAACAGTATT	51317
rs557078568	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935751	TTTGCTAAAAAAAAA[A/G]AAAAAAAAAAAAAGG	51317
rs557113835	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45986931	CAAAAAGAAAGTACA[A/G]TATCAAAGCGAATGC	51317
rs557149598	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055412	TAACTGTTCTACAAC[C/T]GATGGGAAAAGTGTA	51317
rs557159790	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45943724	CTCAAAGCTATCTCC[A/C]CCACAGGAAAAAGGC	51317
rs557172203	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46040551	AGACTGGATTACTCA[C/T]TACTGCAGTACATTA	51317
rs557187104	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46092096	AGAGCCTATTTGCCA[-/A]AAAAAAAAAAAAATC	51317
rs557189517	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45996660	ACATGCTTGAGCAGA[A/T]AAAATGAAAGGCAAT	51317
rs557191753	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46114154	AACACTTAGAAAAAC[A/C]GTATTCCAACTACAA	51317
rs557194470	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004651	ACTTTTCTTCATATT[A/G]GTTTGCATAGCACAG	51317
rs557196659	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097371	TCCCTATCGCTCAAT[C/T]CTTTCCAGCAACACT	51317
rs557216823	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46061090	CCATTGCTTGTTTTC[A/G]TCAGGTTTGTCAAAG	51317
rs557228631	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45987061	CAGGGCCATAATTAT[C/G]AATGCGTAAAAGAGA	51317
rs557228684	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45953747	CAAATGTGGAACATA[C/T]TAATAAAAAGGTTAG	51317
rs557263417	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988615	GCTGCTAGGCCAGGC[A/G]TGGTGGCTCACCCCT	51317
rs557302457	in-del	-/TA			intron-variant	PHF21A	GRCh38.p7	11:46099936	ACAATTTACATTTTT[-/TA]AAAAATCTTTGTAGT	51317
rs557320058	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46096542	CTTTTGACCCACTGC[G/T]CATTTCTTCCTCCTC	51317
rs557356827	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46095260	AAGATCTATACACAC[A/G]TTTGTGCTTTTTACA	51317
rs557364966	snp	C/T	3.38295e-05	0.00411262	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935726	AAGTAACTTCTGTTT[C/T]TCTTCTTCTTTTGCT	51317
rs557371624	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079054	AGTTAAGTACCATCT[A/G]TATTTAAGTATTTTA	51317
rs557380504	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46061975	TTCTATACTGGAAAT[C/G]ACTGCTTTTCAGAAT	51317
rs557382046	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122085	TGCAGCCGCAGCCGA[A/G]GCGAGGCCGGAGCCC	51317
rs557395689	snp	A/G	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:45961204	GAATTTGCAACTCCT[A/G]TTCTTTTTGGTATAA	51317
rs557400162	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46088824	CTGTTCTCAAATTCT[C/G]TAAGGAGGTTCTTCT	51317
rs557402231	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970566	ATTCTTGTTCAAGTA[C/T]TTCCTCCTTAAAGGG	51317
rs557428042	in-del	-/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46046132	CTCCATCTTTTGCTA[-/T]TTTTCAGGGTTTGTT	51317
rs557432768	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088130	CAGTTTATAGCATCA[A/G]AAGAATTATTGGCTA	51317
rs557436875	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097192	TAAGGTATATTCTCT[C/T]GCAAGCCAGAGTAAG	51317
rs557442503	snp	A/C	0.0103295	0.0711199	intron-variant	PHF21A	GRCh38.p7	11:45953009	GTTACTATTTTCATC[A/C]CTACTTTTATGCTTC	51317
rs557446471	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46012742	TCTATCTTAATATCC[C/T]ACCAACAACTCAAAT	51317
rs557453510	in-del	-/C	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46114682	TAAAATTTAAAAAAA[-/C]ACACACACAATTTAG	51317
rs557470895	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070697	TCAAAGACTACAGAA[G/T]GGTCTATCTCTCTAA	51317
rs557501234	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036157	TCGGAGATGAGTGAA[A/T]GGGAAGAATCAAGGA	51317
rs557505987	snp	A/C/T	0.00756529	0.0611122	intron-variant	PHF21A	GRCh38.p7	11:45982251	CATAAGCCACCACGC[A/C/T]CGGCTGAGAGGTTTT	51317
rs557515903	snp	A/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46095013	TACATATCAGCATAG[A/G]TACACCTTTCTTGGA	51317
rs557540271	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043914	AGTAAAAGATGGATC[A/G]CAGCAACTGCTTTAA	51317
rs557541178	snp	A/G	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45979233	CACGTTGGCCAGGCT[A/G]GTCTCAAACTCCTGA	51317
rs557545367	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46060889	AAATCTGTGCCCATG[C/T]TTATGTCCTGAATGG	51317
rs557574957	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46086411	GGCATGAGCCACCGC[A/G]CCCAGCCAGCTATTA	51317
rs557599267	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45969334	AAGTCCTCTGTACAG[A/T]CCCCTAGCCTAAGCC	51317
rs557599660	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46001814	CCTGTTTGCATTCCA[A/T]TTTTAACTAGAGGGA	51317
rs557626738	snp	A/G	0.000185718	0.00963455	intron-variant, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935173	CTGGTCAGGAAAACC[A/G]GGAAATGCAATCAGC	51317
rs557626773	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944448	TTCAAAATAAATACC[A/G]AAAAATTATGTCACT	51317
rs557661865	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45949579	TCCCATAAGAAATCA[C/G]AATCAGGGACAAGTC	51317
rs557681610	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46027488	TTCTGGGATGGGAAA[A/G]CAGTACTACCTACAC	51317
rs557705549	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929193	GGGGTCACAGGAGGG[C/T]CTGGGCCCTTAAGGG	51317
rs557707760	in-del	-/TTAAT	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46007714	TAAAATTTAGTTACA[-/TTAAT]TTAAATCAAAAAACG	51317
rs557734278	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46087041	AAGATAATAATACTC[C/T]GAGCTGTCTAGAATT	51317
rs557735792	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45987388	CACCTGAGGCCAGGC[A/G]TGGTGGCTCACACCT	51317
rs557747669	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044657	TGTGCTTTCACTCAT[A/G]AACATTCTCATTTCT	51317
rs557759257	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46037566	CAATCGCTTGAATCC[A/G]GGAGCCGCCTCTGTT	51317
rs557761335	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46008194	TACGCCCATACACTC[-/T]TATCATGTGAAATCC	51317
rs557766544	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044083	CTACATTTGAGAAGA[C/T]GGTAAACTCATCATA	51317
rs557769955	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026728	AAAAACCTGAGACAC[A/G]TTGGCTTGGCAATCG	51317
rs557782190	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46059881	ACAGGCACCCACCAC[C/T]ACGCCCAGCTGATTT	51317
rs557783917	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46069550	ACACAAGGACTATAG[A/G]ATCTAACTTACTTAT	51317
rs557819607	snp	A/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46018722	ACACATTTTTTTTTT[A/T]AAATTCAAGAAAACA	51317
rs557826701	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46047492	AACCGAGACAAAAAG[G/T]TAAATGACTTTTAGT	51317
rs557856987	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46080319	GCACACCAGCACACC[C/T]GGTTAATTTTTTAAT	51317
rs557859186	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46019607	ATTGCACTCTATTCA[C/T]CTGTGACCAATTTTT	51317
rs557868295	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978500	CTTGCAAAATGTTGC[A/G]CATGAACCAGTCCAA	51317
rs557908783	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46062092	CTGTTTTTTGTTTTG[-/T]TTTTTTTTTTTCCTC	51317
rs557994083	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46121984	AGTGCAGCGGCGGCG[A/G]CGGCGGCGGTGATGG	51317
rs558005240	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035388	TGCCAGCATCATACC[A/G]TTCACTGACTAAACC	51317
rs558014830	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45981505	ATGGCTCATAAAGCA[C/T]ATAATAACTATTTGG	51317
rs558018230	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960251	ACAGCAGAACTATGC[A/C]CAATAGCCAAAAAGT	51317
rs558046024	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45967369	TGAGACCCTGTCTTA[-/A]AAAAAAAAAAAAAAA	51317
rs558051599	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46016266	GAACAATCTTTCTCA[A/G]AAAGGGATATCACCA	51317
rs558066901	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984751	AAGAAACTCCAAGAC[A/C]CTGCCCTCCACAACT	51317
rs558069155	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042606	GGACATGGTGCTAGA[C/T]CTGAATGTTTGTGTC	51317
rs558086760	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995507	CCCGGGTTTATAAAA[G/T]ATCAGAGCACTTGTC	51317
rs558088841	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005392	AATATTTGCACAATA[A/T]ATTAACGCCTTGTAT	51317
rs558121887	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45996037	TAACCTCAAACTCCC[C/T]GGCTCAAGTGATCCT	51317
rs558192948	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45968231	TATTCTCTGCACAGA[A/G]GCAAGAAGGAATTTT	51317
rs558245647	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019463	CACACAGCCCTAAGA[C/T]GTGGCCAATCCAGGC	51317
rs558256455	snp	A/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120246	GTTTTCCAAAAAAAA[A/T]TTTTTTTTAATTAAA	51317
rs558308854	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994215	CAACATTTAGACTGG[A/G]TAAAGTGTTGGGCTC	51317
rs558309794	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990742	AGAAGACTTTATTTT[G/T]AGAGCAGTTTTAGGT	51317
rs558317121	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46091930	GACATTTTTGGAAAA[C/T]GGGACTTTTACATTT	51317
rs558333391	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45969189	TCCTACCAAGGAAGT[A/C]AACACTCCTCAAGGT	51317
rs558391384	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015759	CAATATTACTGTCTT[C/T]TACCTCTATACCTTA	51317
rs558401024	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933871	AGAACCAAAAGAATT[C/T]TGCACTTTCCAGAAA	51317
rs558418813	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101763	AACTCAGCCTCCCTA[A/G]TAGCTGGGACTACAG	51317
rs558460877	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099282	CTGATGGAGCCCTCA[C/G]TATACTACAGTCCTT	51317
rs558463437	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45976826	GTCAAAGAGCCAGAT[C/T]CTGTCTAAAAAACAA	51317
rs558474848	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46115210	CCACACAAGTCTAGT[G/T]TAAGAAAGTTGCTTT	51317
rs558483751	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46047639	GATATTATTTTTTCT[C/T]TGCAATGTTCTGACA	51317
rs558486673	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46015059	GACTGGTGTAAAGTG[C/G]TATCACTGTGCTTTT	51317
rs558495303	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094404	GTCACTCAGCTAGCT[C/G]ATAGTGAAGCTGGAG	51317
rs558498082	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107486	TTGGCTGGTAAAAAA[C/T]GTTGACTACTCTATA	51317
rs558512932	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45960252	CAGCAGAACTATGCA[A/C]AATAGCCAAAAAGTG	51317
rs558521271	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998405	TATGCCTACTGAGTA[C/T]ATAGTATTGTAACAG	51317
rs558543641	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973284	ATCACTGTGCAATAC[C/T]AGTGAAAAGTACCTC	51317
rs558593405	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45965036	TGACGGAGGGCAGCA[C/G]AGCCTGTCTGTGAAT	51317
rs558606829	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45947066	ATCTCTAAAAATTGG[C/G]GCTGTTTAAAAGTCT	51317
rs558611429	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982104	TGGGACTACAAGAGC[A/G]TGCTACCATGCCCAG	51317
rs558614332	in-del	-/C	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45960184	ACTCCTAGGTATATA[-/C]CCTAAAGAACTGAAA	51317
rs558629943	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105634	AAAAAACACAAAAGG[A/G]ATGAATGAGTCTAAG	51317
rs558632749	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998815	ATGAGCCACCACACC[C/T]GGCCTTTTTTTGTTT	51317
rs558641354	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008025	GGTACTAAAGTAAAA[C/T]GTGTTTAATGTTGTT	51317
rs558658799	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46073879	CTGCCAGAGTTTCTT[C/T]CAGAAATCTCAAGTT	51317
rs558712513	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45980697	ATTTTTTGCATATGA[C/T]AACACAGATACTAGC	51317
rs558719232	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46114474	GCACACAAATTTAAC[A/G]CAATCCAGCTAAAAA	51317
rs558722094	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46088659	TACTTCATAAGACTG[C/T]TGTGGTTTAAATAAG	51317
rs558726862	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46038862	AATCACCTCTTAAAG[G/T]CCCCATCTTTCAGTG	51317
rs558734020	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45961987	GAAGTTGGTTATGTC[C/T]GACAGGGGAAGGACA	51317
rs558745072	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46098536	TTGCTTCCTCACTCT[A/G]TAAAGTACAAAAATC	51317
rs558754903	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931080	CAAAACAGCTCACAT[C/T]TGAATGTCAGGAAGA	51317
rs558775292	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089760	TCTAAATGTCTGAAT[A/G]TATGTGAGTATAAAA	51317
rs558820555	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930741	CAGTGGGCAGCCGCT[C/G]CAGCTCTCTGAAGTG	51317
rs558859243	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46082235	GAACACATTTTCTAT[A/C]CAGTAAGCTCAATTT	51317
rs558864821	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070993	TATTTGGAGATACAT[G/T]GTTAAAAATTTTTTT	51317
rs558892005	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46090538	GAGATTCACAATGCA[C/T]ATTAGCATATTAAAG	51317
rs558899371	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062300	TTTTCTCTTCTCCAT[C/T]TTCTCTGTTCCCTTG	51317
rs558901403	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071945	ATAAGCAGAGCAAAA[C/G]ATCGGGTGGATAAAA	51317
rs558922647	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45972715	GGTCAGGAGTTCGAG[A/G]CCAGCCTGGCCAACA	51317
rs558928718	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945338	ATTTGACAGTTTTTC[C/T]GGAACCTGTTTCTGA	51317
rs558932644	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46020755	CCTATAAAGCCATGA[C/T]AGTTATGGTTGAAAA	51317
rs558933024	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46097095	TCTCCTACCACCTCC[C/T]TGGTCCAAGTCACCT	51317
rs558950019	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45936932	AGCCACTGGCAGTTT[C/T]GTCCTTGACCTGACA	51317
rs559007027	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054449	AAAATCCACTTACCT[A/G]CTCCTACACATCTTT	51317
rs559008198	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945576	CCATCTGTTTTCTGA[A/G]AACTCATTCACAGTA	51317
rs559060212	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062886	TCAAATTAATGTTAT[C/T]TGTAACAGCTAAAAA	51317
rs559061568	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46021411	TTAAACTATTAACAA[C/G]TATACACCATACCTC	51317
rs559068328	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944915	GGGATTACAGGAGCA[C/T]GCCATGCCCGGCTAA	51317
rs559096012	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45962884	GGCGACAGAGCGAGA[C/T]TCTGTCTCAAAAAAG	51317
rs559131353	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984636	CTTTTGTCAACAGAG[A/G]AGGGAGACGGAGAGA	51317
rs559133517	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123410	CTTTATGGTACATGT[G/T]TAGGCCATTTAGTAG	51317
rs559133951	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45960032	AAAAGGAAAGTAATA[G/T]GTGTGGTAAGGATGC	51317
rs559146063	in-del	-/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45994213	GGCAACATTTAGACT[-/G]GGTAAAGTGTTGGGC	51317
rs559187294	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071276	CCCAGGTAGCTGCTG[A/T]CCCTTCATGCAAGGC	51317
rs559193599	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45994717	TTTCAACTCTGTGCT[C/G]AGCTGGCAAAAGCTC	51317
rs559229090	in-del	-/A	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46060075	AAATTTATGGAACAG[-/A]AAAAAAAGACTTAAA	51317
rs559276954	in-del	-/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46055244	GCAAATTTTTAGTAA[-/T]TTTTTTTTATCATTT	51317
rs559285475	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028259	CATGTACTCAGGACT[A/G]TCCCTGAACTTTTAA	51317
rs559307316	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45974241	CCCAGGTAGTGCTTA[C/G]ATCTTTACCCCTACT	51317
rs559311392	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45953154	AGCTGAGTGAACTAG[A/G]TATCTTATAAATGTT	51317
rs559314818	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087718	AGAAGGGGTCTCATA[C/T]GTTGCCCAGGCTGGT	51317
rs559348570	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013833	CTACAGTAAAAATAC[A/C]CTACGAAAGATGAAA	51317
rs559350005	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054709	TGCCACTAGAAGGTA[A/G]GTTCCTTAAGAAGAG	51317
rs559367392	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45981970	TTTTTTTTTTTGGTT[A/G]TTTTGAAACAGGGTC	51317
rs559377339	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114676	ACTTATTTAAAATTT[A/T]AAAAAAACACACACA	51317
rs559408678	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036856	TACATCTGTTGTTTA[A/C]ATAGCATTTTTTATG	51317
rs559414059	in-del	-/T	0.0150606	0.0854603	intron-variant	PHF21A	GRCh38.p7	11:45991273	ACAGTAGTACCTTGA[-/T]TTTTTTCCATATGGT	51317
rs559419768	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45950788	CATACTCACAAAACA[C/T]GCAGAGAGTTTTAAA	51317
rs559422345	in-del	-/AAC			intron-variant	PHF21A	GRCh38.p7	11:46117662	TATTATAGGGATGAT[-/AAC]AAGGCTTAAAGCCCT	51317
rs559429061	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45941462	AATATCTGGTAAACC[C/T]CACTGTTCGGTCTTG	51317
rs559461388	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029087	TGTAGCTTGCAAAAG[A/T]GTGTTATCTGTCATG	51317
rs559492982	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934739	GCAGCATTTAGGAGG[A/G]TCGAAGCCCCAAGGA	51317
rs559507746	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46006832	TGGAATAATATTTCT[A/G]TTCTTTCCTTCAAAG	51317
rs559563455	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46050480	AGCTGCCGAATCACA[A/G]AAAGCAACAAGAAAT	51317
rs559569995	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45962279	TATTTAGCCTGGTCA[C/T]AGAGAGAACGTTGGA	51317
rs559574550	snp	A/G	0.140242	0.224618	intron-variant	PHF21A	GRCh38.p7	11:46021074	TTTAAAAAAAAAAAA[A/G]AGAGAGACAAGGTCT	51317
rs559585143	snp	A/G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970021	CTACAAGCTTTCATC[A/G/T]TAAGTTAATCATCTG	51317
rs559598181	snp	A/C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46048626	AATACAAAAATTAGC[A/C/T]GGGCATGGTGGCATA	51317
rs559632568	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46003958	ATCTTTATGAAAATA[C/T]GTATCATCCTCAGAA	51317
rs559634144	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46012054	TCCCTCACACTAGAC[C/T]CCTTTTCCTTTTTAC	51317
rs559640418	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46082780	TGAAACAAAATATTT[A/G]GTAATTAACTTCAAT	51317
rs559643942	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089395	TTTATTAAAAACTTT[A/C]ACATTTATTAACATG	51317
rs559655574	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46115836	TAAGGATACAAAATT[C/T]AAAAGCACATTAATA	51317
rs559675326	snp	C/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120476	GCCGCCTCTGTCACC[C/G]GCTCCGGCCCTGCAC	51317
rs559689481	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995799	TAGACAAAAACAAAC[A/C]AAAAACATAAAGCTG	51317
rs559720771	snp	A/C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052860	CTTACCATGATGAAT[A/C/G]AGCAAAGGCATCACA	51317
rs559738514	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46103964	ACTCCTCAAATCTGA[A/G]GAGATCATTGTACCT	51317
rs559739270	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46014342	CTGCAAAGGATATTA[C/T]GTTGTTCTTTTTTAT	51317
rs559740181	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112736	TTCCATCCAACCTTA[C/T]GGAACAACTATCCCC	51317
rs559745697	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46000667	TCTCACGTCTGTAAT[C/T]CCAGTACTTTGGGAG	51317
rs559757654	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052027	GAAAACAGTCAAAGG[A/G]ATAGTCAATAGTCAA	51317
rs559774016	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112004	ACTAGTTTGGATATT[C/G]TAACAGTGCAAACAT	51317
rs559798895	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45987497	AAACTCCGTCTCTAC[A/T]AAAAATACAAAAAAT	51317
rs559812884	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032332	TAATATTTTTCTGAT[C/T]TTATATAACAATCTG	51317
rs559844192	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46060225	CTGGTCTCAAACTCC[C/T]GGCCTCAAGCAATCC	51317
rs559850728	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932412	CCTGCACCAAGAAGA[A/G]AGCACGGTCTTTTCT	51317
rs559853460	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041288	ATAAAAAGTAAGGAG[C/G]GTGGAAAAGATAAGT	51317
rs559884879	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991929	TGAAATCTCACTCAC[A/G]TGAACATGTAAACTG	51317
rs559887621	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960543	CGGCAGAGGGCAAAA[A/G]TTAAATAATTGCTTA	51317
rs559905470	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46095943	CAGAAGATTCAATCT[C/G]TTCTCTTCCCCTTAC	51317
rs559939162	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46018852	CTGCATACCATGACA[C/T]GCTCTCACAGATGCA	51317
rs559967589	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122216	ACAGCAGTTTGAAGG[C/G]GGGGGGGGAAAGCCG	51317
rs559971290	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068981	TCTTTCTCAAAGAGA[C/T]AGTAAAATCTTTGAC	51317
rs560011183	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983384	CTTTCTTTAAAAGAT[A/G]GCGTTGGTATGTCAA	51317
rs560034097	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009119	AGCTGGGATTACAGG[C/T]GTGCATCACCATGCC	51317
rs560053105	snp	G/T	0.00993419	0.0697739	intron-variant	PHF21A	GRCh38.p7	11:45943149	TTTTTTTGAGACAGG[G/T]TCTTGTTCTGTCACC	51317
rs560100609	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45956093	TTCTTCAAAAATGGA[A/G]AAATTAAGACATTCC	51317
rs560107146	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46090960	AAATGGGTTAAGGTC[A/G]CTTCTCTAAGATTCC	51317
rs560113058	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972977	CAGCTACTCGGGAGG[C/T]TGAGGCAGGGGAATC	51317
rs560122608	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991096	TGCCTCCATAGTTCT[A/G]CCCTTTCCAGAATGT	51317
rs560143166	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100526	TTCTTAAGTATAATT[G/T]TTAAAATATATATCT	51317
rs560192506	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041998	AAATCCTGTATGTCT[A/G]TTTAAGTGTTAAAAA	51317
rs560210643	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46067567	TAAAACACTGAAGTA[C/G]GAAATAATAATAAGA	51317
rs560247776	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45973440	TATGCGCATATACAC[A/G]TATTATCTAATCTTT	51317
rs560248097	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45974772	GATTTATTTATATGA[A/G]AGCTGTGATTTGTTT	51317
rs560268355	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46106785	GGCACTGCCATCTCA[A/G]TGGGAGTAGAAGCTA	51317
rs560268505	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097640	CTAACTATCCAAATC[C/T]CACCCACACACTAGG	51317
rs560281590	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116719	CTATAATCCCAGCAC[A/T]TTGGGAGGCCAAGGC	51317
rs560295863	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46082320	ACTATTTCGTCAAAT[A/G]TATGTTCTGGCTTTG	51317
rs560303018	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101217	TGTCCAGCAGGCATC[A/G]TTCTTCACTAAGTTA	51317
rs560324441	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46077433	GATGAGATACACAGA[A/G]CATGATTGCCTTTTA	51317
rs560353598	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105882	TTAAAACAAAAAACA[A/T]GACTATTGCAGTATA	51317
rs560356857	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048546	AGGCCGAGGCAGGCA[A/G]GTCACCTGAGGTCAG	51317
rs560360673	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46023261	TTCCATAAGGCAGGC[C/T]GGGATCTGGCAGAGA	51317
rs560373918	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45981250	AATTAGCCAAGCATG[A/G]TGGCACACACCTGTA	51317
rs560383935	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46103410	AATTATTTAATTGAA[A/G]GATAACTATACAACC	51317
rs560384885	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46082527	ATAAATAAATGTTTA[C/T]AATCACACAAGCAAA	51317
rs560431126	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098700	ATCAGTTAACCTCAG[A/G]ACTAAAACTCTTGTC	51317
rs560461611	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45948590	TTTACATGGGGTTCT[A/G]TTCACTGTGCTATTC	51317
rs560475069	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46066342	CATACATATAAATAT[A/G]TATTAGATATTTATC	51317
rs560476791	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45947416	TTATATTAGGATTAT[A/G]CACAAGAGTCATGAT	51317
rs560481781	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031558	TAGTTCATGCAGCCG[A/G]TACGAATTCATTCTT	51317
rs560490922	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030684	AAACATAATAAAACC[A/C]ATTTTCACTAAATCT	51317
rs560502386	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46020894	TTATGATGGGGTTAT[A/G]TCCTGATAATTCCAT	51317
rs560503625	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46022609	TGGGACTACAGGCAC[A/G]TGCCACCATGCCAGT	51317
rs560510601	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45998983	AGGCACCTGCCACCA[C/T]GCCTGGCTAATTTTT	51317
rs560534663	snp	A/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46073455	CTTGATGTTAAAAAA[A/T]TTTTTTAAATCTTAT	51317
rs560551276	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45960919	TTGAAGAAGTCTCCA[C/T]GTGATAAAAGTTTGT	51317
rs560566321	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089908	TGGGCCAGGCCAGGG[C/T]TCCCCATAGCACCCT	51317
rs560569258	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073062	ACACTTCAGCATTAC[A/C]TCACGCCTGTAATCC	51317
rs560608473	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955433	CTCTTTGAATAGGAA[A/G]GAGAGAAGTATGATG	51317
rs560614372	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014630	CCCACCAACAGTATA[A/T]GTGTTCCCTTTTTTC	51317
rs560625215	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45990106	ACAAAATCTAATCCA[C/T]AAATTTCTACACAAA	51317
rs560642394	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040421	CAAAATAACTTAGCA[A/G]TCTAATTATAAGTAG	51317
rs560671963	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45964574	CTTTTTAAAGCAACT[G/T]TCTTGAGAGAGAATG	51317
rs560679212	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048338	GTATCATTCTATATG[G/T]AGTACTTCATTCCTT	51317
rs560694025	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930309	AACCACCTCCATGCA[C/T]GCTGCCTGTTGGGCC	51317
rs560703987	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46067093	ACCTTATGTATTACT[C/T]ACTTATGTATTACTT	51317
rs560727835	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116592	TAAATTATGAGAAAC[G/T]GACTAGGCAGCATTT	51317
rs560728163	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46002059	AGTGACTATTTTTAG[C/T]GAAAACAAAACAGTA	51317
rs560742405	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056338	TTTCACTGGCTTGGG[C/T]TGTGTGGGTCAGTTT	51317
rs560762927	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46046059	CTCAGCTTTGTGAGC[C/T]CTGGCATTCAGCTAG	51317
rs560767159	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998597	GGCTCGGCGCAACCT[C/T]CACCTCCCAGGTTCA	51317
rs560772398	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46026954	TTGGAACACAGAAAA[G/T]CTGCTTTTGCTAGCA	51317
rs560776975	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46101319	TAAACTAACAATGTA[A/T]GAAAAGAACATTCTC	51317
rs560789241	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022535	GGCATGATCATGGCT[A/G]ACTGCAGCCTCAAAC	51317
rs560792981	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038504	TCTTGAAGGAGGTAA[A/G]GGAGTCAGTTGTGTG	51317
rs560839573	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46102843	AGCTTAAGGTTTTGA[A/T]AATAGCTCAGTATCT	51317
rs560841455	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46064016	AATTTCAAGTTCTGT[C/T]GATTAACACCCTCCC	51317
rs560858296	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939034	GAGACGGGGTTTCAC[A/G]TGTTAGCCAGGATGG	51317
rs560867839	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46105555	AAAATGAATGTCACT[A/C]TGAAAATATCCCAGT	51317
rs560880095	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099819	CTGTTTCCAGCCTGA[A/G]AGAAAATTAGAATCT	51317
rs560923248	snp	A/G	4.9516e-05	0.00497549	intron-variant	PHF21A	GRCh38.p7	11:45979976	TCTTTTCTACCAAAT[A/G]AAGACAAAAAGAAAT	51317
rs560944863	snp	A/G	1.67556e-05	0.0028944	intron-variant	PHF21A	GRCh38.p7	11:45938325	ACCCTATAAAGTTGA[A/G]AGGAAAGGTAAGAAA	51317
rs560967418	in-del	-/AACT	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46046408	AAAAGAGAAACCAAA[-/AACT]AAAACAAACCAAACC	51317
rs560982404	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45989066	TCGTCAAACAACAGG[C/G]AGGGTGCAAGTTCCT	51317
rs561008257	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46019219	AACTGCTTTTTAATT[A/C]TTTCTAGAAGATAGG	51317
rs561025976	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021705	CACCACTATGCCCAG[C/G]TAATTTTTATGTTAT	51317
rs561059454	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099922	AAAAATGGTTCCATA[A/C]AATTTACATTTTTTA	51317
rs561102597	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105007	TAAGCTTCAGTACCA[C/T]TTATTTAGTACTTAC	51317
rs561104456	snp	A/G	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46114581	CAACATACTGTCCAT[A/G]AGGCCAGAGATAGCA	51317
rs561120445	snp	A/C	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46098603	TTTCTGAGTCTAATG[A/C]TCATAACGAAAACTT	51317
rs561167338	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45998875	TTGCCCAGGCTGGAG[G/T]GCAGTGGTGTGATCT	51317
rs561177488	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972842	TTGCTTGAACCCGGG[A/G]GGCGGAGGTTGCAGT	51317
rs561191561	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955159	TTTTATGCACCTCTT[G/T]TTTTTGCATCCCTTT	51317
rs561196873	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055702	GAGTCATGGAATCTC[C/T]TTATATAAACGCCCC	51317
rs561204305	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030564	TCATTAGTCTGTTCT[A/C]TGAATGTTACTAAAA	51317
rs561211812	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073323	ACAAAGCGAGACCCC[A/G]TCTCAAAAAAAAAAA	51317
rs561226021	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46056151	TAATTTAATGCCTCC[A/G]GTTTTGAATTTCATC	51317
rs561232713	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089817	GAGGGGGTGGGGGGC[A/G]GGTCCTCATTTTTTA	51317
rs561250445	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45939518	AAGCAACAGCTGACA[A/G]TGTTCTCCTAAAACC	51317
rs561251531	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007482	CCATGTCCAGCTTAT[G/T]TTTGTATTTTTAGTA	51317
rs561270411	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988385	CGTAGCAGGCAGTAT[A/G]TATCATGTAGAAAAT	51317
rs561279535	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930265	AGCGTGCTGCAGACA[C/T]GGTCACCCTCACGGA	51317
rs561287820	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006752	CTTAAACGCCTATTA[C/G]AATGTGATATACTTG	51317
rs561302197	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030089	GTTGTTATTCATTAC[A/G]GTCTTTGGACAAAGA	51317
rs561330725	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089161	CAATGTTTAAAGTAG[A/G]TTTAATTCATTTTTT	51317
rs561340467	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038443	CATTTCATTCTTTCA[A/G]TAACTATTTATTGAG	51317
rs561341786	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46062823	ACTAAGGCATTTACT[A/G]AAGAGAAATGAAAGC	51317
rs561365260	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46097533	AAAAGAATACTAAAA[C/T]AAAGACTAAAACTAT	51317
rs561370471	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45989005	TACAATCACTTAAAG[-/A]AAAAAATGAACAATG	51317
rs561379108	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46080470	ACTTCTTAAAAAGAA[A/G]AAAAAAAATTTAAAA	51317
rs561383622	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45963212	GTCGCCTGAGGTCAG[C/G]AGTCTGAGACCAGCC	51317
rs561403382	in-del	-/ACTA	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45940358	CCACCACCACGCCTG[-/ACTA]ACTTTTATATTTTTA	51317
rs561464413	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945367	GATCAACTCTGCTCT[A/G]AAGAGCAGAGTTTCT	51317
rs561502367	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101450	AGATTGGCAAAATGC[C/T]GGTAATTGTTAGTTA	51317
rs561502520	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111106	ACAAATTTTAAATCA[C/G]AACTATGTGGGGGGG	51317
rs561542099	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929610	GGGCTGAGGACCCAC[A/G]GACACCGGAGAGAGG	51317
rs561589613	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110320	GGAGTACACTTAAGA[C/T]CAAGTCTTCTGACAT	51317
rs561597626	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045285	ATTTCTTTTTCCCTA[G/T]GAAAGATCATAAGCA	51317
rs561599825	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054632	ATCAAAGACTAGATC[G/T]TATTACTCTACAACT	51317
rs561600395	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959780	CGGAACAGGAGAAAA[C/T]ATTTGCAAATCATGT	51317
rs561604070	snp	A/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46018461	AAATCTATAGGGGAA[A/T]AAGAAAAGAATCTCC	51317
rs561634526	snp	A/G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035841	AAAAGAGAGGTTGGA[A/G/T]AAAGTAGGTATGTAT	51317
rs561663631	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45936073	ACTTGAGCCCAGGAG[A/T]TTGAGACCAGCCTGG	51317
rs561665949	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46101936	AATCTCGGCTCACTA[C/T]AACCTCTGACTCCTG	51317
rs561668041	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967994	ACAACAAGTGGGTCA[G/T]GATCCACTGTTTGAA	51317
rs561690089	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941516	AATGATGGTTTAGTA[C/T]CATTATGAAAATAGC	51317
rs561721904	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:45992923	CCTCTACCACTGAAC[C/T]GCAGCTACCTCAAGT	51317
rs561737056	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957464	ATGGAAAAAAACTAG[A/G]AATTAATGACAGCAG	51317
rs561739463	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46077066	ACATGAAGTTTTATA[C/T]TTGAGCATCTTGTAC	51317
rs561756586	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050082	TTCCCCAGCAGAGTT[A/G]GCGATTGCCACTAGG	51317
rs561758841	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46001718	TATGATAGGCCATGG[A/G]AGAATAAAACCAATA	51317
rs561763116	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46020054	AAAACAAAGATACTA[C/T]TGTGAAGGCAGGTTT	51317
rs561768521	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46076416	AGGTAACAAGGTACA[C/T]GCAGCACCTACAAGA	51317
rs561802017	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026927	AGGTCCACTGGAGAG[A/G]CTGTTGAGTGTTTGG	51317
rs561805713	snp	C/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930981	GGGGCCTCTTCTTTA[C/G]AGTAAAGCAGTGTTT	51317
rs561815123	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949263	AAAAATGATAAGTCA[A/G]AAAAAATCTACCACT	51317
rs561817862	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45971973	CGCCTCTGAGGTAGT[C/T]ACCCTGGAGGCAATG	51317
rs561830556	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46086683	ATGTGTCCAAAATGA[C/T]TCCTTATAATTTTTG	51317
rs561876912	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45948814	TATAATGATGGGAGG[A/C]GGGAAGGAGAAGAAA	51317
rs561895659	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067299	ACAAGTATCTGAAAA[A/G]TCTAGAGGGTAAGGT	51317
rs561910641	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46002531	TATTTGGGGGAAAAA[A/G]AAAGGAATTCACACA	51317
rs561942921	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059180	GTACAAATATTTACG[C/T]CCAAGGATGTACACT	51317
rs561949536	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041128	AAACATGTATAAAAA[G/T]CCACCTTCTTATTCT	51317
rs561954186	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46042798	TAGCACCTTCTTGCT[A/G]TGTCCTCACAGCAAG	51317
rs561990398	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46042379	GCCATATTAGTATGT[A/G]TGATAGTGCAACTCC	51317
rs561997392	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46009209	CAACTCCCGACCTCA[A/G]GTAATCTGCCCGCCT	51317
rs562000032	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46058374	CTTTGAAAGGATATT[C/T]TGAAGGGCAGTTCAA	51317
rs562013167	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009270	TGAGCCACTGCGCCC[A/G]GCCATTAGTTCACAT	51317
rs562015003	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017267	TGAGCCACCACGCCC[A/G]GCCTACATCTATTAA	51317
rs562017529	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45993839	TCAGAGATGAGGCTC[A/G]GGCAGCTGGCGAGAT	51317
rs562026218	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45998501	GTACATGCAAAATAA[C/T]TCTACCATTTCTTTT	51317
rs562048566	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45955865	TGAAGAAGTGAGGTC[A/T]GCCAACAACCATGTG	51317
rs562062273	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46031720	ACTCTTTTTTCCTCT[A/G]GCTTTGTCTGTTAGG	51317
rs562098139	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46107218	ATCATACATTTAACT[A/G]GTAACCATAATTTTT	51317
rs562098809	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46066682	CCAGCTTGGGCGACA[A/G]AGCAAGACCTTGCCT	51317
rs562101166	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45966899	TGGGATTACAGATGT[A/G]AGCCACTGCACCCAG	51317
rs562103494	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46016570	CCCTTCCCTAATCCC[C/T]TACTCAGGATTAATA	51317
rs562123363	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46114133	CACACACACGCTTCT[A/G]CAAAGAACACTTAGA	51317
rs562138908	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091737	CTTTTTTTAAGAGAT[A/G]AGGGTCTCGTTTTGT	51317
rs562157863	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46000196	ACATATTTAGCACGA[A/G]GAAACTGCTACACTA	51317
rs562166063	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46032013	CAGCTTTATTAGCTG[A/G]TAATTTAAAACACAG	51317
rs562178409	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992817	ATACGTTTCATAATG[C/G]TGCCTACTTTATCAA	51317
rs562179089	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010066	TTTAGTTGCTTAACC[A/G]TATCATACTAAAAGA	51317
rs562197905	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966517	TTAAAAACATGAGGT[C/T]AGCCTTGCTTGGGTT	51317
rs562224702	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024057	ACAGTTTGGGAAATA[A/C]TGGATTAGTTGCAAT	51317
rs562229112	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46088686	TAAGGCAAAATTATA[A/T]GAAAAGCCCTTTGCA	51317
rs562242801	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983304	GTCCTTGAGAGGAGG[A/G]AAAAAAAAAAGGAAA	51317
rs562257784	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45974614	AGGTGCTACCACACC[C/T]GGCTAATTTTTTTTA	51317
rs562261184	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984803	CTGCTTTTTCACACA[C/T]TCAGTCACTCCACTG	51317
rs562296723	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46070821	TGGACAAACGGCAAA[A/T]TCTTTGAAAAATATA	51317
rs562300160	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46100341	AGCATGGGGTCCCAT[C/T]AGGCACCCTATTTTA	51317
rs562306990	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982520	TTCTATTTCTCCAAT[A/G]TAAAAGGCAGAATAA	51317
rs562321892	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932267	GTGGCTGAAAGACCA[A/G]AAGCAGCACCAAAGG	51317
rs562330701	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45950129	ATTTTCTATTCCAGG[A/T]ATTCAATCAAACATC	51317
rs562332988	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46118451	GCCCCTGGAATATTC[A/G]TAACATGTTAGCCAG	51317
rs562337758	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933548	GACTTGTCTTCTCTA[C/T]CTAAACAAACGGCTC	51317
rs562341944	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46091129	CCCAGTCCCCAAAAG[A/G]AAGAGAGACACCACA	51317
rs562343970	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991730	TACCCAATCTTGGTC[A/T]CAGCTTCTGCACTCA	51317
rs562344619	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092510	CACATAGAAATGAAA[A/T]GCACCTCATTTAAAT	51317
rs562382414	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46003788	TTAAAAGCTTCATTA[C/T]ACTCTGCAGACATTT	51317
rs562392608	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46005196	ATCCAAAACTTTTTG[A/G]GCACTGACGTGATGC	51317
rs562466230	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110044	TAATTTTTTGGTTCT[A/C]ACTCATTATTTAAAA	51317
rs562476055	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46033399	CCTCCCAAACAGCTG[C/G]GACCACAGGTGTGCA	51317
rs562492025	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933452	CCCTCTTCTGGGCAC[C/T]GGGGTTGGTGAAATC	51317
rs562503815	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101817	ATTTTTGTATTTTTT[A/G]TAGAAACAGGGTTTC	51317
rs562533951	snp	C/G	1.66341e-05	0.00288388	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965477	GTGGATGGAATTCTG[C/G]GATGTGGGAAGGGTT	51317
rs562542900	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085534	CAAAAGTCTGTTTTT[C/G]CCTGAATAAATTTAA	51317
rs562558778	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46106048	GGACCTAAAGGTACT[A/G]AGAACCTGACACAAT	51317
rs562559733	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45976375	AAAATAGAAACTCTC[C/T]GATTTGTGAATTTAG	51317
rs562581566	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084928	CTCGTGATCCACCCA[C/T]CTCAGCCTCCCAAAG	51317
rs562600606	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46034634	GGTGACTATCCAGCT[A/C]ATGACAGGTCTCCCA	51317
rs562612586	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46093302	TTTGTTGACTGATAT[C/T]ACTCCAATAGTGTCT	51317
rs562636880	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042754	TAAAAGAGGCCTATG[A/T]AAGCTTGTTTTTCCC	51317
rs562653063	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057448	CATTAGGGCTTAATT[C/T]TCCCAATGAACCCAG	51317
rs562659488	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009751	TTAGTCACTGCACAA[G/T]ACAATTAATATAATT	51317
rs562659777	in-del	-/TTAT	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932901	CAGCTTTTCTATTCC[-/TTAT]TTTAGTTTTTGTTAC	51317
rs562670422	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45956268	CTAGATGAATAAATA[A/T]AAAAGCCAGTGTTAT	51317
rs562687277	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939979	GAAGGTCTAATACAG[A/C]AATTGTGCACAAGAA	51317
rs562703036	snp	G/T	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931313	TGGGCCCAGACAAGT[G/T]GAGGGGAAGAGCTCT	51317
rs562704588	in-del	-/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46088320	TATCAGCAAGGCCAC[-/T]TTGCCTAGCCCAAAA	51317
rs562758394	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932625	CAAATAGCACTTTTG[A/T]AATTTTTTTTTACAA	51317
rs562765556	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930896	AGCGTATGTCTCAGG[C/T]GGTCACAGGCCCCCC	51317
rs562767599	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938821	AAACTTCAGATAAGG[G/T]GGAGACTAGTGTATT	51317
rs562785427	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45940553	AAAAAGATAACATAT[A/G]TTCTAAAATATTACA	51317
rs562808404	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46066444	TGTGGCTTGAACCTA[C/T]AATCCCAGTTACCTG	51317
rs562813002	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46082660	TCCCTTTTGAGTCAA[C/G]AAATGTAAATTTAAA	51317
rs562815312	snp	C/G	0.000194571	0.00986143	intron-variant	PHF21A	GRCh38.p7	11:46049361	ATGCCCTCACCATTC[C/G]TTTTGATCCATTAGG	51317
rs562852152	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091000	CAAAGTAAAGAGCTA[C/T]AGGATCTTGATTATT	51317
rs562855038	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46063377	GATTGGCAAACTTTC[C/T]AAAAATAACCAGATA	51317
rs562874798	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015420	AATTCTTTGCCTAGG[A/C]CAATTTCCAGAAAAG	51317
rs562877994	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46023300	ATGGCTAATTACTGA[G/T]GCCCCTTCTATTTTG	51317
rs562893629	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974514	GCTAGAGTGCAGTGG[C/T]GTAATCACAGCTCAC	51317
rs562927195	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079415	AAATCTGGACAGAGA[A/C/T]GGGTGACAGTGGCTT	51317
rs562937263	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45983971	CATGACTGCTGCTGG[-/T]TCACTGACGAAGGTT	51317
rs562938603	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46030774	TAATTTGTAACTTTA[A/G]GAAGGTGACGATCAT	51317
rs562962284	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048071	CACAGTTGCACAACT[A/C]CAGAATTAATTCCAG	51317
rs562976712	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46107764	AAGCTGGAATCAAGA[A/G]TTCTATTTAATGTAG	51317
rs563013125	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45970621	CTTGGGCACTGACAC[A/G]GTTAATTTGTGAGTT	51317
rs563067641	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990984	ACAGCCACCATTATA[A/C]TATCACACAGAGTAG	51317
rs563068611	snp	C/T	0.0111196	0.0737302	intron-variant	PHF21A	GRCh38.p7	11:46075224	CTATGTTAGTTCTCA[C/T]AAACAAAAATTTCGA	51317
rs563072755	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040363	CAAAGAAAAATACTA[C/T]TTGGCACAGACAATA	51317
rs563075203	snp	A/G	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:45998739	CTGGTCTCGAACTTC[A/G]GACCTCAAGTCATCC	51317
rs563075263	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45962112	TGCCTGCTCCAAACA[C/T]ACTAGAAACTGAGTT	51317
rs563087508	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932779	AAACAGTGCCCGAAC[A/G]ATGACACAAGGACTC	51317
rs563107193	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45990293	AAACAGGATCTCACT[A/C]TGTCCCCCAGGCTGG	51317
rs563118412	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039279	TGGAGAATTTGTTTC[A/G]ATTACTCAGCTTCAT	51317
rs563162290	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044134	GTTTCAACCTAAGCA[C/T]TACTGTTTAAATGAG	51317
rs563163548	snp	A/G	0.00247689	0.0351043	intron-variant	PHF21A	GRCh38.p7	11:46049385	CATTAGGTTGAACCC[A/G]GCCCAAATACATACG	51317
rs563169219	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031668	TTTAGATTAATAGGC[A/G]CTCCGAGGCAGGTCA	51317
rs563177292	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45961200	GCTGGAATTTGCAAC[C/T]CCTGTTCTTTTTGGT	51317
rs563186322	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46016490	CTCTCATGCAACACC[G/T]TTCCTACCTGTCCAA	51317
rs563245626	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46020994	TGTATGATGGGTTTA[C/T]TGGACCATAACTCCA	51317
rs563316218	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45977410	CCAAAGTGTTGGGAT[G/T]ACAGGCGTGTGCCAC	51317
rs563321465	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45979124	TGGGTTCAAGTGATT[C/T]TCCTGCCTCAGCCTG	51317
rs563342742	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035925	AGAAGACACAGAGAG[G/T]TTTTAAGCAACCATT	51317
rs563361093	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935316	GCGCTACACTCCCCC[C/G]ACACACTGTCAGGAA	51317
rs563413977	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45975119	AGGAGTTTGAGACCA[G/T]CCTTGGCAACATAGT	51317
rs563420732	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46048039	GAAGTGTAGAATTCA[A/G]TGGCTTTTAACATAT	51317
rs563438457	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119822	TGACGAGAAGTGTTG[A/G]GAACTGCGTGCACGA	51317
rs563452975	snp	C/G/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:45970913	TGCACTGAATTTAGT[C/G/T]CTTGGTGTCAGGACG	51317
rs563507956	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45995719	TTAATACTGCAGACT[A/T]AAGCAGAAGCTGAAC	51317
rs563509808	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45986244	CTAGCCTGATTGAAA[C/T]GCAGTTTTCTTATTT	51317
rs563535448	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941794	TGCTTTGCTAGGCGC[A/T]GAGGACGTATGTTTT	51317
rs563553259	snp	C/G	1.78376e-05	0.00298638	intron-variant	PHF21A	GRCh38.p7	11:45969764	AGAAAGAGCCCATGA[C/G]GATTTCTGTCCCATC	51317
rs563582277	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46002691	TTTGGACTCTGTCCC[A/C]GTAAAATGTCCTATG	51317
rs563595964	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028060	TAGTAGCTGATTCTC[C/T]AAATTCTTGAGTTGG	51317
rs563622117	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018777	AAAAATGATGATGCT[A/G]TACCAAGAATAACTG	51317
rs563630179	in-del	-/TC			intron-variant	PHF21A	GRCh38.p7	11:46115518	AATGTTAACATATTA[-/TC]TCTTTTTTAAAAAAT	51317
rs563630252	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46079588	GATTTGGCAGGTCTA[C/T]TGGTTTGTTTCTTAC	51317
rs563652785	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46103075	CCGGCTGGACAGGGT[A/C]CTGCAGAGCTGAAAT	51317
rs563661953	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930003	CTGGAGAACCCAGGC[C/T]CTGGAAAATGCACCT	51317
rs563676498	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45950897	CACAATGCTAACTCA[C/T]AGCTAAATGATTTTC	51317
rs563676499	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120316	GGGGTGGGGTGGGGG[A/G]GATGGAGGAGCCCCA	51317
rs563721500	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46043366	CACAGGTTACTTCTG[C/T]TTACCCACATCATCA	51317
rs563728722	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45939908	AAGGGAAGTGCTAGA[A/G]GTGACCCAGCAAGTC	51317
rs563764945	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46086742	ATTTTTCAAATATTC[A/G]TACTTCATTCTACTG	51317
rs563779487	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934657	TGGACTGAGCTCTCC[A/T]GGGTGGAAAACACAC	51317
rs563795320	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112650	AGTTAAAGCGTACAG[A/G]TATTCAAGATGTTGA	51317
rs563807256	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961282	GTATACTTTATATAC[C/T]TGTCTGCATGAAAAA	51317
rs563814506	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46010734	ACAAGGAAAAAGATA[C/T]ATGTATTTCTGTGCC	51317
rs563844861	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45943028	TCTCATAACCTATAT[G/T]CAATCCTGATGGCTC	51317
rs563855750	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076262	CCGAAGTTTTTTCAC[A/G]TAATAGTAGGTCAAT	51317
rs563873109	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46068390	TACATATATATAATA[C/T]ATGCACATTATTTGA	51317
rs563897316	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45934501	GAGTACTAACGCTTA[A/G]AAACAAACCGGCAGA	51317
rs563898057	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45967825	AAGAAATATATTTTA[C/T]TCTGTAATCAGCATG	51317
rs563917036	in-del	-/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45964441	TAAGGCAGCAGGCAG[-/C]CATCTGAACAGCCTC	51317
rs563919406	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46077217	ACTACATGCTTTACA[A/G]CATTATCAACAAAGA	51317
rs563921663	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977982	ATTATGTAACCTCTC[C/T]GTGCCTTAGTTTTCT	51317
rs563939443	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960444	AAGCAGCCATAAGAG[A/G]TCACATATTGTATGA	51317
rs563961413	snp	C/T	0.000200003	0.00999808	missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934045	CCGGCGTGGAGGTGG[C/T]GGCATTGGCAGGGGG	51317
rs564000766	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959700	CAAAGTTGTAGGGTA[C/G]AAGATCAAGACAAAA	51317
rs564017360	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076975	GTGGCCATAATACCA[C/T]CACCTAATGCACAGA	51317
rs564032180	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46069112	ATATATACAACCTCT[C/T]GATCTTCAGAACTTT	51317
rs564043656	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46027940	ATCTCATGCCAAAGG[A/G]AAGCAGCCAGCACCT	51317
rs564051419	in-del	-/A	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46016522	CCTTACCCATTCTAG[-/A]AGACCTAGATCAAAC	51317
rs564055980	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46013838	GTAAAAATACACTAC[A/G]AAAGATGAAAAACGG	51317
rs564059399	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45976571	GTAGTGCCAAGCGCA[A/G]TGGCTCATGTCTGTA	51317
rs564080699	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46027039	GAGCAGGAACACACA[C/T]GCACACATGCACGCA	51317
rs564116879	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058742	TCTGTACTAGTAATA[C/T]GGTCCCCTGGCTCAA	51317
rs564118652	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985226	TTGATAAGTCACACC[A/C]ATATTCATCAACGCT	51317
rs564149209	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46042803	CCTTCTTGCTATGTC[C/G]TCACAGCAAGAAGGT	51317
rs564163554	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102004	CGGGGATTACAGGCA[G/T]GTGCCACCACGCCCA	51317
rs564176463	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46070243	ATTTAAAATTGAGAA[C/T]GATTCCATAAACGGC	51317
rs564206074	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46081397	TCTTCAATGAAAAAA[A/G]CTCTTGATTTTCCTT	51317
rs564213475	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46078192	TAAGTACGGGCTACC[A/G]ATGCCAGCTCTCAGA	51317
rs564223646	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45941679	CAGAGGAAGTCCTAC[A/G]GAGGCACCATACCAG	51317
rs564230325	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46079416	AATCTGGACAGAGAC[A/G]GGTGACAGTGGCTTC	51317
rs564256970	snp	C/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:46102971	GGGACGGAAAGAGAC[C/T]ATCAAGAGGGTAAGC	51317
rs564266178	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994719	TCAACTCTGTGCTGA[A/G]CTGGCAAAAGCTCTA	51317
rs564266599	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46106162	TCTGTTCCAAGTACA[A/G]CATGCTAACATTTTA	51317
rs564332263	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45946507	TCCTGCCTCAGCCTC[C/T]CACGTAGCTGGGACA	51317
rs564365073	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45977360	CAGGCTGGTCTCAAA[C/T]TCCTGACCTAAAGTG	51317
rs564371975	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035892	GTTAAGATTTTGGAC[A/T]TGGTCCTAAGAGCAA	51317
rs564374134	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46013673	TACTTAAACAAACTT[A/C]GATGGTACAGCCTAC	51317
rs564376961	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46050827	AGTATGTCCAGCAAC[C/T]GAGTATGTGTGCAGG	51317
rs564391528	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45966747	GCCCCAGCCTCCTGA[A/G]TAGCTGGGGCTACAG	51317
rs564402751	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067387	TAAGTGACGTAGTAA[C/T]ATTGCAGAAGAGACT	51317
rs564410360	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45986164	AGGAGATGAGACCCT[G/T]TATTAATATCATTAG	51317
rs564428048	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46001841	GGGAAGAGGATGGAG[G/T]TCTTTGGTTTCTATG	51317
rs564440420	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043563	CTGAAGTGATAAAGA[C/T]GAGCTCTGCCAAACT	51317
rs564461132	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119485	TCAACATATGACCGG[A/C]ATATGATGACACCAG	51317
rs564484234	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46074031	AAGGGAGAAACTGAG[-/T]TAAGTATCAAAGATT	51317
rs564521217	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46118647	TGTATTTTTCAGACA[C/T]TTTTAATGACCCCCT	51317
rs564535715	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45970333	ACTCTCAGTATCTGG[C/T]TGAGTGACCTCGTTG	51317
rs564544252	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46018203	TGCAGTGAGCTGAGA[C/T]TGCGCCACTGCACTC	51317
rs564591836	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056240	TTTGTTTTCATTAAG[C/T]CTTTCTCAAGAGAGT	51317
rs564595630	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46106487	GAATTCTGCTCTGAG[A/G]TGTTGGGGGTTGGGG	51317
rs564602894	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46017463	TTTCTTGCTTTGGGT[A/G]TGTGGACTGATAACA	51317
rs564647332	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949717	TTGAGAGTTTAACAA[C/T]AGACAACACTTGTAA	51317
rs564666555	snp	C/T	0.00438332	0.0466095	intron-variant	PHF21A	GRCh38.p7	11:45975352	TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT	51317
rs564680476	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055544	CACAAATGCTAGCCA[C/T]AGGTTTCTTTCCATT	51317
rs564685484	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007351	GATGGAGTTTCACTC[C/T]TGTCCAGGCTGGGGT	51317
rs564695341	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46092341	AACAAAACACACACA[A/G]GTTTCCAAAGTTTTA	51317
rs564711353	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021645	CTCTTGGGCTCAAGC[A/G]ATCCTCCTGCCTCAG	51317
rs564721398	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46056529	ATAGGTCCTTGTAAA[C/T]GTCTTTCTAAAAGGG	51317
rs564735568	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955116	TATTTCCCCCTTTAT[A/G]CTAAACGCTATGTAA	51317
rs564765094	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076209	AAAGCAAGATGTTCT[C/T]CTCCTGCCCTATATA	51317
rs564784138	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46053050	AAGGGCCTCGAGTAA[C/T]GTGCCCCCTCCCAAA	51317
rs564803490	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966983	CTTTCCCCTTATGCA[C/T]GAAGCTTGACCTTCA	51317
rs564825395	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022410	CAGTGAGCTGTGATC[A/C]CATCACTGCACTCCA	51317
rs564863092	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46043890	CATTTGGATGTGAGT[A/G]CAGAAAACAGTAAAA	51317
rs564921665	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114755	ATTTGTAAGTATGTC[A/G]CTTTGGAGATGCACA	51317
rs564939368	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46006932	GTCAGAACAACAGTC[A/G]GTAAAATTTAAAGAT	51317
rs564956894	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45954623	GTAGCTAGCATACTG[A/G]TAGACTGGGCTTGCA	51317
rs564961302	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079515	GAGTCCCAAACAAGG[C/T]CTGGAAAGAAGCTGG	51317
rs564968643	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45997195	TCTTCCTTTTTCCTA[G/T]GCTTGATGTATGAAA	51317
rs565004961	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46003401	ACCTATCCTCTCCCC[C/T]ACTGCTAAAAGAAAA	51317
rs565037833	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46081017	TTTGCTGTTTCAGAC[C/T]TGCTGTGTGGTACGC	51317
rs565062088	in-del	-/G			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122213	CAACAGCAGTTTGAA[-/G]GGGGGGGGGGGAAAG	51317
rs565068276	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972140	TGCAATGAAACATGA[C/T]AAGGTGAAAACAAAC	51317
rs565094988	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004964	ACTTTTTCCCTTTAC[A/G]ATAATATTTGTCTCT	51317
rs565125950	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123200	CAGAACCAGAAATAG[C/T]CTTGGACTTTACTAG	51317
rs565138264	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122260	CGAGGAGAAGTGATG[G/T]GGAAGCACTGCAATG	51317
rs565148954	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963987	GCAGGTCACTTGAGG[C/T]TGGGAGTTTGAGATC	51317
rs565153983	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45940705	AGAGGGTCAGCCTTT[A/C]TTGAACCTTATCCCT	51317
rs565158186	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45954043	CTCTCGTTGCCCAGG[A/C]TGGAGTGCAATGGCA	51317
rs565167413	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45987576	TGAGGCAGGAGAATT[A/G]CTTTAACCCAGGAGG	51317
rs565168635	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013887	TGGTAGTTGTACTGG[C/G]TGAGTCAGTGAATGA	51317
rs565176684	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46020309	TTGGGGACAACACTA[C/G]AATTCCCTGAAGTGG	51317
rs565188118	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46072142	CTACAGATACAGATA[C/T]GCTACTGTAATAGAA	51317
rs565212053	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45963061	AAAGTAGGGAAAAAA[A/C]CAAATTACAAAATAC	51317
rs565238062	snp	C/G	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929568	TCTGGCCTGCCCGTC[C/G]CATCCCGCCTGACTG	51317
rs565246493	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46086861	ATAACAAAGGGCTAA[C/T]ACAGTTTATATATTT	51317
rs565296058	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013068	TTCCTATATATTCAC[A/G]CCTATGATAAAGTTT	51317
rs565298383	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112757	AACTATCCCCATTTT[A/T]AAAAAAAAGGAACAG	51317
rs565303681	snp	A/G	0.000453176	0.015046	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928883	ATCTTAGCATTGGGC[A/G]GACACCAGGGCAACC	51317
rs565345669	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944320	TCCCCTAAAATAAGT[G/T]TGTATGGTAGGTGAG	51317
rs565377498	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118907	GCTTAGAGTGAACAC[C/T]AGATGTAAACAAATA	51317
rs565393680	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46097492	TCCCTCAAATTATTG[A/G]GGAAATCTACAGCAG	51317
rs565393782	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088531	GGAAAGCACATTCAC[C/T]ATCCCAAAAAACAAA	51317
rs565413408	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037684	TGCTTATCTGATTCT[A/T]ATCCTTTTGTAAGTA	51317
rs565413862	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105062	TTACACATTAACTCA[C/G]TTATTCCTCATAACC	51317
rs565414340	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46116500	CATCACATCAATGGA[G/T]AAATGAAGAAAAACT	51317
rs565420100	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45936152	TCATGGTAGTACACA[A/C]CTATAGTCTCAGCTA	51317
rs565457855	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46061359	AGAACCTCAATGGTC[A/G]TTTAATAGGAATAGC	51317
rs565465216	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45935985	ATTTTCTTCCCCCAA[C/G]AAGTGCTACAGTCCA	51317
rs565482212	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45952078	CCAAAGTGGTGGGAT[G/T]ACAGGCGTGAGCCAC	51317
rs565585922	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46051164	CAAAAAGGATAACTT[C/T]CCACCTTTCAAGTTT	51317
rs565601184	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46045322	CACATTATTATACCA[C/G]GTACTAACACAAAGG	51317
rs565605863	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46021011	GGACCATAACTCCAT[C/T]ATACACTGAGGAGTA	51317
rs565618364	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052965	ACAAGATGAAGTAGA[A/G]GAATAATTCTCACAT	51317
rs565620080	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46062097	TTTTTGTTTTGTTTT[G/T]TTTTTTCCTCTAAGG	51317
rs565620870	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943945	AAACGGAGAGGCATT[C/G]TACAGAAGAACTGGC	51317
rs565641031	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46070487	AGGTGCCCGCCACCA[A/C]ACCCAGCTAATTTTT	51317
rs565655752	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45997742	CATTGTTGGGCCATC[C/T]GTTTATGTGTGCTGC	51317
rs565672615	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113149	CAACTACAGGTCCCA[C/G]CATGCAGTGCTCTAA	51317
rs565674319	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45951577	TGTGGTTGCCAACTA[A/T]CTACATTCCTAATTT	51317
rs565694983	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46079868	GGAAAGGAAAGGAAA[C/G]GAAAGAGGAAAGGAA	51317
rs565726962	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078593	CTCTGTTAATTTTTC[C/T]GTTAGAAAGTAACAT	51317
rs565748337	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45947472	CCTCTCTGTATTAAA[C/T]TGGTGATGCCTATAG	51317
rs565749607	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46035282	CCATCTTTCTCTACT[A/G]ATCTGAAATATTATC	51317
rs565810243	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952212	CAGTGATTCTGTCCA[A/G]CTAGAAGGTGAACTA	51317
rs565814801	snp	C/T	1.67276e-05	0.00289197	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935720	CCATTTAAGTAACTT[C/T]TGTTTCTCTTCTTCT	51317
rs565816999	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044562	TCTCTTACTCTTTCG[C/G]GCAACCCAGATTAGG	51317
rs565832553	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46051706	TGCCTCAACTCAAGG[A/G]GGTGAGGACACTGGT	51317
rs565858503	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46121413	CTCAGCAGCAGCAGC[C/G]AGCACCACCAGCCCA	51317
rs565870107	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961650	CGACATGTTACATAG[A/C]AGTCTTTGTTGCAGG	51317
rs565893551	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46077714	GATCACCCACACCTG[C/T]TGTCCAACAAGTTAC	51317
rs565924332	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46027973	CATTTTATTTGTCAG[C/T]AAGGAATTCATTTCA	51317
rs565925317	snp	G/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45986550	TGCATACTAGGAATG[G/T]TAGTTGTAATATATT	51317
rs565926444	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122473	CGGGGGCCTTCGCTC[A/G]CCTTTATTTATTGCT	51317
rs565960113	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46012558	AGTCTCTGTTTATTC[A/T]CCTCTTAAATGGAGA	51317
rs565970236	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46049789	CACCCATTAGAGTCA[C/T]GAATAGCAAACTGCT	51317
rs565983616	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46043166	AGGTAAGAAATTCAA[C/T]CAATGTAAAGTACAC	51317
rs566005562	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46056991	TGCTTTAAATATAGT[-/A]AAAAAAAAAAGTCAA	51317
rs566035958	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094889	TGGCGACAGAGTGAG[G/T]CTCCGTCCCAAAAAA	51317
rs566049432	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46043807	CCCACATTGAAATGA[A/G]TGCTCACTTTGGACT	51317
rs566063500	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968204	TGCCCACAGTCTTGA[C/T]CATCCCCAATTTATT	51317
rs566064743	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45976636	CACTTGAGCTCCGGA[A/G]TTTGAGACCAGCCTG	51317
rs566067603	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026703	CTGTGGGCTTTTAAA[C/T]CCGTAATTAAAAAAC	51317
rs566094138	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45993255	GTACTATTTTCCACA[A/G]ATATTTCCCTAATGA	51317
rs566107636	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985587	AGACAGGGAGGAATA[C/T]TGGTGGCAGAAGCTA	51317
rs566112802	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45941599	GAGAACTGCTGCCCA[C/T]AGAAATGAATATAAA	51317
rs566125532	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45969127	AAAACTCCTTCTTCT[C/T]CTCCCTTTGTCTGAA	51317
rs566155333	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031034	GCCTACACCAGTGAG[C/T]GAACTTTTACAGGAA	51317
rs566197379	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46109962	CTCCAGCCTGGGCAA[C/G]AGGGCAAGACTCCGT	51317
rs566228606	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46062074	TCCCAATCCCTGTTT[A/G]CAACTGTTTTTTGTT	51317
rs566230013	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111320	ACTAAAAATATAACA[A/G]TTAGCCAGGCATGGA	51317
rs566249952	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059537	TTCAAGCAATCCTCC[G/T]GACTCAGCTTCCCAA	51317
rs566259090	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46007988	GTACTTGGGATTACC[A/G]TGCTCCAGATAAGAA	51317
rs566279169	snp	A/G	0.00636936	0.0560724	intron-variant	PHF21A	GRCh38.p7	11:46110853	TGCAATGGCACAACC[A/G]CAGCTCACTGCAACC	51317
rs566285048	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941209	GCTCAGGTAATCCTC[C/T]CACCTCAGCCTCCCA	51317
rs566286892	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949958	AAAGAAGAGCTCCCC[C/T]AAATGAACAGAAGTC	51317
rs566289953	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933812	ATCAATTGGCAAACT[C/T]TGGTGCCACCTGGCA	51317
rs566304005	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45976568	TTAGTAGTGCCAAGC[A/G]CAGTGGCTCATGTCT	51317
rs566309959	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119761	AAAAAAAAAAAAAGA[A/T]ATCCTAACAGCACCG	51317
rs566356474	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46102135	TGCTGGGATTACAGG[C/T]GCGAGCCACCACGCC	51317
rs566372115	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998763	GTCATCCACCTACCT[C/T]GGCTTCCCAAAGTGC	51317
rs566388451	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039658	CAATTTTAGATCTAC[A/G]AAGGCTGAATTAAGT	51317
rs566388817	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46000453	CTAAAGACAAGTACA[C/T]AATTACCAGAAACTA	51317
rs566389011	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982080	TGTCACCTCAACCTA[C/T]CAAGTAGCTGGGACT	51317
rs566405525	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941828	GAAGCACTCTGGCAA[A/T]ACCAACTGCAATTTC	51317
rs566414089	snp	C/T	0.00358779	0.0422022	intron-variant	PHF21A	GRCh38.p7	11:46051119	TTAGTCTCTCTGAGG[C/T]AAAATACACCACATT	51317
rs566418297	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46081833	CATTTATATATTGTC[C/T]GTGGCTGTTTTCTCT	51317
rs566426258	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091272	AGTCTTGCACTAGGC[A/G]ACTACCCTATTCCAG	51317
rs566446846	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982689	GCTTCAGTCCTCCTC[C/T]CCATCAGACATCAAA	51317
rs566456990	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973241	GACAGTGGAGATAGA[C/T]GGTATTTCCAACATC	51317
rs566512225	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099996	CTATCCTTAATGAAC[A/G]TTTATCTTTTTATCA	51317
rs566539044	in-del	-/A	0.00835141	0.0640778	intron-variant	PHF21A	GRCh38.p7	11:46107738	TCTCAGCAACAAGTT[-/A]AAAACTCTCAAAGCT	51317
rs566550183	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46115884	TGTCTTCACAGAAAG[C/G]TTTACTATTCACTGT	51317
rs566580331	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46004851	TCCCATTCACTACAC[A/G]CATACTTACATGTGT	51317
rs566588040	in-del	-/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46017342	GAAAAAATCAGATTT[-/G]TTTTTTTAGCACTCA	51317
rs566588240	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45961699	AGAAACATAATTCCT[C/G]AGAACTCCATCAAGC	51317
rs566593175	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45973814	CAATCCAGTGCTATC[A/G]TGGATTGTGGGAGTA	51317
rs566598645	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023015	CTTGGCCTCCCAAAG[C/T]GCTGAGATTATGGGC	51317
rs566631624	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45994086	ATGATATACTTCCTC[A/G]TCTACATAGTATGAT	51317
rs566643922	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46046410	AAGAGAAACCAAAAA[C/T]TAAAACAAACCAAAC	51317
rs566671194	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990643	TCCAGTTTCTACATA[A/C]AGCAAAAGTATTGAC	51317
rs566674592	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46087074	TGTCAGGTGCCACTT[C/T]GCAATTTGCTGATGG	51317
rs566701845	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46047624	ATTAAGAGTCTGAAA[C/G]ATATTATTTTTTCTT	51317
rs566718529	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014161	CAACCCTTGCTCCCA[A/T]CCTTCCCTACTCACT	51317
rs566750621	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46099014	TAAGAAAGGTCAATG[C/T]TAGATACCAGATTTT	51317
rs566755078	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021964	CAGGCATTGCACTAG[C/T]AGGAAAGGAAAAGAT	51317
rs566768684	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45978467	TCTTTAGTGTTCTTA[C/T]AAAAAATTCATTCTT	51317
rs566810785	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46011918	TAAAACATTAGGCAC[A/G]AAAATTAGAAGCAAC	51317
rs566816207	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938373	AATTTTAATGTTAAC[A/G]TGCACATTCTAGATG	51317
rs566844256	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45971625	AGTAATAACTGCAGA[A/C]TAATTCAGGCACAGG	51317
rs566860788	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46072309	AAGTTCAGGCCCATG[A/G]GATCTAACTGGAAGT	51317
rs566867887	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013597	GTTGCTTAATAACAG[A/G]GATATGTCCTGAGAA	51317
rs566889209	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45954385	ACATACACAGTCTCC[C/T]ATTTCGGAACAATTC	51317
rs566890113	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46096242	ATCAATTTTCCCCTC[A/T]TCATTACTGGATCAT	51317
rs566900868	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45952094	ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCTAAAT	51317
rs566901321	snp	A/G	0.00557542	0.0525036	intron-variant	PHF21A	GRCh38.p7	11:46055468	GGCATTCAGAATGAG[A/G]AGTGACAATTAAACC	51317
rs566922604	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055185	CTGGACATTAATAAT[G/T]TATCCCATTCTGTTA	51317
rs566937128	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45983967	GACGTCATGACTGCT[A/G]CTGGTCACTGACGAA	51317
rs566942448	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46033501	ACTCCTGGGCTCAAG[A/C]AATCCACCGGCCTCA	51317
rs566944636	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46115051	AAACATTTCTGTAAC[C/T]GATTCCAAAGTATAG	51317
rs566950476	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46021246	TTTTATTTTTTGTAG[A/T]GATGGGGGTCTCACT	51317
rs566971951	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929658	CTGGGGAAGGGGTAG[C/G]GGGGTGGGGTCCTCA	51317
rs566972888	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46063372	AGTAAGATTGGCAAA[C/G]TTTCTAAAAATAACC	51317
rs566981581	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988495	ATTGGGAAGTATTTT[C/T]AACAAAAGTACATTC	51317
rs566996207	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45959893	CAAAGGATTTGAATA[G/T]ACCTTTTTCCATGGA	51317
rs567004952	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088814	GTAGGCTTTTCTGTT[C/T]TCAAATTCTCTAAGG	51317
rs567016485	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46092530	CTCATTTAAATAACA[C/T]ACAACTACTCCTTCA	51317
rs567029604	in-del	-/A	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46093359	AGCTTCATGTCTCCC[-/A]GATTGTAAATCTTTG	51317
rs567069646	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089284	AAATACTTCCTACTA[C/T]GTATCTAATATGTAG	51317
rs567093126	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46038095	CCTCCCTGTATTGAG[C/T]TTACTTGTATACTCC	51317
rs567154493	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930505	GGAAGAAATCAAAAC[C/T]CCAGAGGAGCTCAGC	51317
rs567161195	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46030144	CTGCTGACTCTATCT[A/G]GAGAATATCTTGCTA	51317
rs567172067	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079742	GGAACAATACAAAAC[C/T]CTATCTAACTCGATT	51317
rs567175404	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46046288	TAGCACTGGGGCCAT[C/T]CTCCTATGGGGCAGC	51317
rs567206877	snp	A/G/T	0.00716625	0.0594738	intron-variant	PHF21A	GRCh38.p7	11:46089580	GCAACCCTGATTTTC[A/G/T]AGGCGAACCCTCTGA	51317
rs567259366	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990529	CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGTG	51317
rs567289784	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021316	ATCCTCCTGCCTTGG[C/G]CTTCCAAAGTGCTGG	51317
rs567294978	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098263	TGGGTGTAGTAAACA[A/C]TGATTATCTATTACT	51317
rs567296234	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45989390	CCAGACGCGGTGGCT[C/T]ATGCCTATAATCCCA	51317
rs567301590	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007039	CGTTCCTGCAAGCTC[A/G]TTTTACAGGTGATTT	51317
rs567305178	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45990508	CAAGCGATCCACCCG[C/T]CTCAGCCTCCCAAAG	51317
rs567312812	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107024	GCTGTCCCCACGGCT[A/G]CCTCTTCTGCAGGAA	51317
rs567327179	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46020472	GGAAGTGCTTACCAG[C/G]CTTGTGGATTACTGC	51317
rs567348258	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46034306	TGTAAGACTAATAAC[C/T]CTTTGTCACACATGT	51317
rs567361493	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45979072	CCCAGGCTGGAGTGC[A/C]GTGGTGTGATCTCAG	51317
rs567379035	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972556	ACCGAGGCAGGTGGA[C/T]CGTCTGAGGTCAGGA	51317
rs567381112	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030357	CAAGACGATCCTGCA[A/C/T]GATCTTTTATTCTTA	51317
rs567397243	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930940	AGGTCTGAGGGGACA[G/T]TGAAGGACAGGGAGA	51317
rs567398668	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013491	CGTGAGTAACTAAAG[A/C]CACAGAAATGGAAAC	51317
rs567417248	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937552	GTGGTGTGACCTCCG[C/T]TCACTGCAGCCTCCA	51317
rs567436779	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46114854	TACTGACAGTTTGTA[C/T]TCTCAATGCAGCCAA	51317
rs567440345	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054252	AGTCAGAGTATTAAT[A/G]TGATAGTAACCCTTG	51317
rs567462704	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998732	GGTCAGGCTGGTCTC[A/G]AACTTCGGACCTCAA	51317
rs567474187	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46114193	CTCTCATCCACTGAC[C/G]TCTTCTGAAAACACA	51317
rs567482049	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45987778	GAGCAAAACGTCTGT[C/G]CCTCTGTAACTGTCT	51317
rs567497572	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46055126	ACTTTTAAATTATGG[C/T]GAGAACTTAAGATAC	51317
rs567500533	snp	A/G	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:45984211	AAGACGGAAGGGAGA[A/G]AGGGAGAAAAAATTA	51317
rs567511527	snp	A/C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46018550	CTATCCTGAAATAGC[A/C/T]GTCTGTGCATAATTT	51317
rs567540000	in-del	-/A	0.00716266	0.059414	intron-variant	PHF21A	GRCh38.p7	11:46035423	GTATGTTTTGACTCT[-/A]GTTGGTTACTTCATT	51317
rs567558363	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029399	AAGGATTAAAAAATT[A/C]TTCACTGGCTGGGCG	51317
rs567564660	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45955042	TATCAATACTGTGGC[A/G]ACCAGTGCTCTGGGG	51317
rs567570681	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45987020	ATCTAGGTACATCCC[A/G]GATTTCTTATACCTC	51317
rs567586189	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088785	TTCTCTACATAGTAT[A/C]TATCTAGAAGACTGT	51317
rs567643583	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961846	GTCTTCTGGCTTCAT[C/T]TACTTTTCTGTCTAA	51317
rs567675446	in-del	-/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46058153	CACCTCCCTACATTC[-/T]TACTGCTGCCTTACC	51317
rs567682452	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017619	CATCTCCTCAAAAAA[A/T]CCAAACTGGAAAAGA	51317
rs567690245	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45970373	GGATTCCTGGATAAG[C/T]GGTGAACCTTCACTT	51317
rs567698165	snp	C/T	2.48154e-05	0.00352237	intron-variant	PHF21A	GRCh38.p7	11:46079091	TTTTATTTTAAATTA[C/T]TTTTAAATTTAACAA	51317
rs567723415	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016964	TTACTAAAAATGTTT[A/C]ACCTGGATTTTTTTT	51317
rs567743845	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46015013	AAATAAAAAAATAAA[A/T]AAAAATAAAAAAATA	51317
rs567812324	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45996305	AGGTAGTAAAGCTTA[C/T]AGGTTGACACATTAT	51317
rs567817855	snp	A/G			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123248	AATAATATTTCTATT[A/G]CCTTGTTATGTATTT	51317
rs567820596	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46055176	AGAATCCTTCTGGAC[A/G]TTAATAATTTATCCC	51317
rs567851115	snp	C/T	0.0146672	0.084371	intron-variant	PHF21A	GRCh38.p7	11:45944877	GTTCCAGGGATTCTC[C/T]TGCCTCAGCCTCCAG	51317
rs567855106	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037776	AACTTGAACAATACT[G/T]GAAAATTTTAGCAAC	51317
rs567891716	in-del	-/C	0.394538	0.203982	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930905	TCAGGTGGTCACAGG[-/C]CCCCCCCCCCTCCCC	51317
rs567942197	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46028613	GAGTCTCGTTCTGTC[A/G]CCCAGGCTGGAGTGC	51317
rs567948509	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978388	TAGGGTGAGGAGTAT[A/G]TCCATTATGTAAAAC	51317
rs567957978	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100768	CAGAAATAAGTCTAC[C/T]ATTACCTTGTAGTGA	51317
rs567961643	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958059	CACACATTACCAAAA[C/T]TGACTCAAGATAAAG	51317
rs567962108	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45982940	GAAAGGGTGTTTTTT[C/T]CTCCTCTACAGCCAT	51317
rs567997648	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45973242	ACAGTGGAGATAGAC[A/G]GTATTTCCAACATCA	51317
rs567998144	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928995	CCCCTTGCTGCTATT[G/T]TATGGCTGGGGACTG	51317
rs567998784	snp	A/T			synonymous-codon, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934145	GCCGTGGATGAGGCG[A/T]ATCAGCTGTTTTACC	51317
rs568024778	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118917	AACACCAGATGTAAA[A/C]AAATATCATAAACAC	51317
rs568027178	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46059079	AGTTAGATTCTACTA[C/T]ACATACCAAAGAAAG	51317
rs568049557	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025500	ACATTTTCTTAATCA[C/T]GTATAGCTCTGGACT	51317
rs568081507	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46108226	TGCTCTCTTTATAAG[C/T]AGCTACTAGAATAAA	51317
rs568090324	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46002557	ACACATGGCCTTTTT[A/C/T]ATTTAAGGGCAGAAA	51317
rs568090676	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074804	CACCGTGCCTGGCCA[A/G]TAAAACTATTCTAAA	51317
rs568106137	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45947868	CTTAGGGTTTCCCAT[A/C]TAAATATTTTTGAGT	51317
rs568132453	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107891	TACTGAGTTATCAGC[A/G]TAGCATTTGGTAGTG	51317
rs568195107	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46109302	CTGTGAGGATTAAAA[C/T]TAAATAAGATCCTAT	51317
rs568224306	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966705	GCTCACAGCAGCCTC[C/T]GCCTCCCAGGTTCAA	51317
rs568248561	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932954	GTAAAATAAAACTTT[C/T]CTTAAAGAAAAAAAG	51317
rs568252940	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024566	GGACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC	51317
rs568272947	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992255	GAAAATTTTTCAGCC[C/T]GGCATGGTGGCTCAT	51317
rs568289589	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032553	ATCTTTATTCACTTA[C/T]CTGAATCCTTCCTGA	51317
rs568314035	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46083073	CAAACTGGGTATTCA[A/G]CACACCTCTATGTTA	51317
rs568314059	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46073200	AGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	51317
rs568359713	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092597	ATTAACAAATTAAGG[C/T]AACATCACTAGTTCT	51317
rs568368666	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45946866	CAAAATTCAAGTTAA[C/T]TATTCTTATCCCTTG	51317
rs568408725	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116953	GCCTGGGAAACAGAG[C/T]GAGACTCCGTCTCAA	51317
rs568425169	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46117542	TCTATATTAGAATCA[C/T]AGTCTGTAAATCCGA	51317
rs568430068	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955659	AAAAGTACAATTATC[G/T]CAGTGTTATATAAAT	51317
rs568430611	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931898	TGGTTTTCTCAAGGA[A/G]AGGCCACAACCGGCC	51317
rs568489438	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939304	TTCACAATATGATAC[A/G]AACAATTCTCATCAC	51317
rs568505188	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008622	GTGGAAATGTGACTC[A/G]GTTTTGTGTATGAAA	51317
rs568517508	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040711	GAAACTGCATACTAT[G/T]TTGGAGAGCAAAGGA	51317
rs568550353	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45961429	ACTATTGCACCAGTA[C/T]TAAAATGGGGTAAGG	51317
rs568555988	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001218	CATGTATGGTTCTGG[C/T]AGAGAATCTGAAGGG	51317
rs568566614	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022950	GAGATAGGGTTTCGC[A/C]ATCTTGGCCAGGCTG	51317
rs568573645	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45937471	AAAGTGAAATGGGTG[C/T]TGTTTTATTATTAGT	51317
rs568590254	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45959969	AGTCATTAGGGAAAT[-/G]CACATCAACACTACT	51317
rs568606618	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048713	AGGCAGAGGCTGCAG[A/G]GAGTCAAGATGGCGC	51317
rs568608984	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023306	AATTACTGAGGCCCC[G/T]TCTATTTTGAACATT	51317
rs568626154	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46068789	GTCATTCCATTTGCC[A/G]GCACCAAAAATACGT	51317
rs568646700	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015837	CTTCTATGGTAACAA[C/T]GCCTTCGTCTGAAAT	51317
rs568671332	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45991277	GTAGTACCTTGATTT[C/T]TTCCATATGGTCTAA	51317
rs568746067	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007757	GAAGTGAGATGTGTA[C/T]CCTTTACATAACCTA	51317
rs568787726	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46046445	ACCAAAAAACCTTGC[C/G]ATGACAGCCTCAACA	51317
rs568792162	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46076746	GCCCCCCTCCCCTTT[C/T]CCCCTACCTGTTTCT	51317
rs568798541	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45964135	CCTGGGAGGCGGAGG[C/T]TGCAGTGAGCTGAGA	51317
rs568801452	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46100912	AGCAGGTAGTCAAAA[C/G]TCCCTCCTTGACAAA	51317
rs568814206	snp	A/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45974855	TTCTCCACAGTTTCA[A/T]GATGGGGTCCTTTAT	51317
rs568828878	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46066945	ATACTGAATTATACC[A/G]TATGTCTGTTTTACA	51317
rs568830188	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074077	AATAAGAACTAGTGT[C/T]TACCGCAAGAAATAG	51317
rs568833537	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45998638	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	51317
rs568835928	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45961927	GAGCCACAGTGTAAC[A/G]TGGTTTCTAATAAGG	51317
rs568847499	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45965954	ATAGCCTTAACTCGC[A/T]TTTGAAATTTCTTCA	51317
rs568855055	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46032433	TGTGAAAATCAGTAT[A/C]ATCTACTTCCTTTTC	51317
rs568870108	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46084109	AGAGATGGACTTGTT[C/T]ACTAATCTTAGCCAT	51317
rs568907924	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091937	TTGGAAAACGGGACT[C/T]TTACATTTTAACAGG	51317
rs568976064	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46116835	GGGCGTAGTGGCGGA[C/G]ACCTCTATAATCACA	51317
rs568991669	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45966681	CTGGAGTGCAGTGGC[A/G]CGACCTCGGCTCACA	51317
rs568998959	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982132	CAGCTAATTTTTTTA[A/T]TTTTTGTAGAGATGG	51317
rs569003560	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46108118	GGTTTGCCCCAATTC[C/T]TGCCTATTTACTTTG	51317
rs569005591	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930736	GGGCCCAGTGGGCAG[A/C]CGCTCCAGCTCTCTG	51317
rs569048710	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46031942	TGGGCCACACAGTTA[C/T]CCAATTTTCCCCAAT	51317
rs569073969	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931109	GAATCCACAGCCCAG[C/G]TGCAGGCGAGGTCAG	51317
rs569090981	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46041377	TTGGGCACTGTGCGT[A/T]CTTCTTTCGAGCAAT	51317
rs569103682	snp	A/C	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084881	GAGACGGGGTTTCAC[A/C]GTGTTAGCCAGGATG	51317
rs569104119	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080677	TCTTTTTTTGTTTTT[G/T]GTTTTTTAAAGATGG	51317
rs569115421	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062405	ATCCCCCTTTGTCTC[C/T]TCCATCTATTTATTG	51317
rs569156248	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100621	ATGCCAAATAACATC[A/G]TAACATTAAAGACAC	51317
rs569161626	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45964620	TTCTTCTTTCTCATC[A/C]CTAGTCGTTTTTCAA	51317
rs569163470	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45954507	TAAGAGTGGGCCATC[C/T]TGCAAGAGGCTGACT	51317
rs569202982	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45959439	TTTATGAAAACACAG[C/T]TAACATCATACTCAA	51317
rs569212714	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931765	GTACAGAGCCTCCAC[C/T]GCCCTCCCATCGGCC	51317
rs569217039	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46081609	AGGGGTAGGACAGGA[C/T]GAGCTGGCCAACTTA	51317
rs569228270	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963540	CTCTCTTTAGATTAC[C/G]GGGAAAAGCACCTTC	51317
rs569244595	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46060823	AGCTCTTTAGTTTAT[C/T]TGGATCCCATTTGTC	51317
rs569278923	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112299	TCTGATCAAATTATA[C/T]TGTAAAAAGAGAGGA	51317
rs569300335	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45947695	CAGATACTGCCCACT[A/G]TCAGGCCAATTATTG	51317
rs569313792	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45942723	CAAAGGTAACACTTT[C/G]TTTGTTACCTCTGGA	51317
rs569320775	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45956630	TTGTTAAAAACGTAT[G/T]AATGTTTACTGTAAT	51317
rs569320861	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008530	GGTCAAAGGTAGAAG[A/G]CGGGAAAAGAGTCTG	51317
rs569329475	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46047676	TGACAAGAAGGCAGT[G/T]ACTAACAACCAGAAA	51317
rs569330635	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972461	CTGATTTGGCAGCCA[C/G]TAGCCACAAGTTGCT	51317
rs569356034	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46028141	ACAACAAAAAAAGAA[C/T]TGAAAAAGTTGTGCA	51317
rs569377852	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46065431	GCAGTGGTTGCCGAC[A/G]TGCTGAGCATGGCAG	51317
rs569379551	snp	A/C	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:46007310	CCATCTACCTTTTTT[A/C]TTCTTCTTCTTTTTT	51317
rs569396624	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45986230	AGACCTTTTATTTGC[A/T]AGCCTGATTGAAATG	51317
rs569399883	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46062238	ATTAATCTGGAATTA[C/T]ATGCCCTTCGGTTGT	51317
rs569419187	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055885	AAATTGAATAGTTTT[A/G]TTTTGCTAATTCAGA	51317
rs569421546	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46073164	AAACCCGGTCTCTAC[C/T]AAAAATACAAAAAAT	51317
rs569478204	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097132	TTCACCTAGATAATT[G/T]CAACAGCCTCCTAAC	51317
rs569512762	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076477	TTACCCCATCCCCTA[C/T]AGGTAAACTATAGAG	51317
rs569531843	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122385	CCACCCCGCCCCCTT[C/T]CCAAATAACTACCCT	51317
rs569532229	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45957721	CCTAACTTTACACCT[A/T]AAGAAACAGAAAAAG	51317
rs569547267	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086085	TTAGAAAGGGAGACA[C/T]ACTATGGTGAACAAA	51317
rs569551924	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45973026	GAGGCTGCAGTGAGC[C/T]GAGATCACACCATTG	51317
rs569565678	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960882	TGGCAACTTTTAAAA[A/C]CATCTGGATTTCAGG	51317
rs569586502	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004262	AAACCAAATAACTCA[A/G]TGCAAAAGAGCTCTT	51317
rs569602100	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46030828	GTGTGTGCGTGTGTG[C/T]GCGTGTGTGTGTGTG	51317
rs569618859	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46060538	AAATTCTAACCACTC[A/G]TTGTGGTTCTGATGT	51317
rs569629327	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960102	AAAATGATTTAGCTG[C/G]TGTGGAAAACAGTTT	51317
rs569678009	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46121238	CTTCCCCAGGCAAGG[G/T]GGGGTGGGGAGGAGG	51317
rs569681257	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46109525	AATAAAATTTATATA[A/G]TTAGTAAAATAAAAT	51317
rs569681294	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46072316	GGCCCATGGGATCTA[A/T]CTGGAAGTGGTGCAT	51317
rs569698305	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934902	ATGCCATGGGTAGGT[A/G]TGGTGAGGAGGAGAA	51317
rs569717176	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45942642	TCTGTAACCACCAGC[A/G]ACGTCTAAGGAAGGA	51317
rs569717937	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933642	ACAGAAACAAACCCA[C/T]CGTGGCTGTGGAGGC	51317
rs569727040	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053129	ATTCAAAATTTGTAA[G/T]TAAATGTAATGTGTA	51317
rs569737461	in-del	-/TA	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931003	CAGTGTTTTGGAATT[-/TA]TGAGTGCAGAATGTA	51317
rs569750101	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45938593	ACTGAACCCTATAAA[C/T]ATGTTTTTCTATACA	51317
rs569774370	in-del	-/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45945630	GGCTGAGTTCCATGA[-/G]GGTTATATTTAACAT	51317
rs569808501	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45968115	GTAAAGTGCCTAGCA[C/T]AGTACCTAGTATGTA	51317
rs569813239	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46052247	GCTGTAAACCTAGAG[C/T]TGCCAGAGGCAACCT	51317
rs569828064	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011275	GGGCAGATCACCTGA[A/G]GTCAGGAGTTCAAGG	51317
rs569833544	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018660	ATATGTCACATGACT[A/T]GGCAAAAGATAATTT	51317
rs569834687	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085230	GATATTTTAAAATGT[A/G]TCTATCGTGTGTAAT	51317
rs569868867	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026646	ATGCAAAAAAAAAAT[C/T]CTTTAAAGTCAAGCA	51317
rs569872613	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46117228	AGCAGATTTATCAAA[C/G]TTTCTAGCATCCCCA	51317
rs569872620	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46080594	GTGTTAAAGTTCTTA[A/C]ATCCACATTGTAGTT	51317
rs569897811	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46057836	TGCCAAGTGTAAAAA[C/T]ATGGTGCTTAAGGGA	51317
rs569908376	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092995	CCTGGGCTCAAGCAA[A/T]CCTCCCTGCCTCAAC	51317
rs569926349	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46017583	TTGCCCTTAAGGGGG[A/G]AAAAAAAAAAACACC	51317
rs569943954	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46019041	CAAGAAAAAGAAAGG[A/G]GGAAGAAAATAAGCC	51317
rs569967615	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042468	CGTTATAAGACTGGA[C/T]TAAAATCACTGAATG	51317
rs569991990	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102072	CATGTTGGCCAGGAT[C/G]GTCTCAAACTCCTGA	51317
rs570059505	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46049690	TGACAAAGAGCAGCC[A/G]CTGTCCTACTCAGGG	51317
rs570083204	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46034216	GCCTTAATATTAGTG[C/T]CCCCACCCCCCCCTT	51317
rs570110422	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46111235	GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC	51317
rs570125052	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001407	TGTACTTAGCCAATG[C/T]ACCTGTAGATTCTAA	51317
rs570137680	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949046	TGACTGTCAACATGC[C/G]GACTAGTTAGTGCTA	51317
rs570162407	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042832	GTGCTATCTATGAAG[C/G]AGACAGTAGGTCCTC	51317
rs570176017	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120753	CCCCCTACCTCCCCC[A/C]ACAACAAACTCCAAG	51317
rs570186479	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985256	TGAGGATGCAGGAAG[A/G]AGACAGGGCAGTCTT	51317
rs570194241	snp	C/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46002877	AAACAAAAAAACACC[C/G]AATGTATTTAACATT	51317
rs570213524	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46067615	AAAAAAAAAAAAACT[A/G]AATTGAATCATTTAA	51317
rs570233558	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46109622	TTTATAATATACACA[C/T]AAATGTACCAATGTG	51317
rs570243131	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118760	AATTAAAATGAATAA[C/T]AGTATTTCCAGTAAA	51317
rs570255990	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958617	TCTCCAAAAAATAAC[A/G]AAAAAAATTAAATTA	51317
rs570277668	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45940341	GCTGGGATTACAGGC[A/G]CCCACCACCACGCCT	51317
rs570345993	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110613	TTATATTTAGCCCTT[C/T]GTATTAACTCCTTTG	51317
rs570352857	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949335	CAGGTTTTCAGAGGG[A/G]AGGCACTGAACAGCT	51317
rs570353123	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46092846	CACTGCAGCCTCAAC[C/T]TCCCAGGCTCAAGCA	51317
rs570360276	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46003341	TGTGTCTAGTCATCA[C/T]TCAGACTCTCTTCGG	51317
rs570373317	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:45968034	CTAAACCTTAGATTC[C/T]TTACCCTAAAAAGAG	51317
rs570406346	in-del	-/C	0.00597247	0.0543191	intron-variant	PHF21A	GRCh38.p7	11:46059576	ACTACACACATGCCA[-/C]CCACACCTGGCTAAC	51317
rs570419148	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46051417	GAGCATTTACCATTA[A/C]CTCCCACCTCCATTC	51317
rs570423930	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959874	AACCCAATTTAAAAA[C/T]TGGCAAAGGATTTGA	51317
rs570429036	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085928	TAACATCAAAATACT[A/C]AAACCTAAAAAAGAA	51317
rs570433534	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967298	GCTTGAACCTGGGAC[A/G]TGGAGGTTGCAGTGA	51317
rs570452880	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46068727	CCAGTGTCAACATAT[A/G]TAACACCTGATGACA	51317
rs570456532	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076448	TCTCTATCACCTATT[C/T]TCACTAACTGCCTTT	51317
rs570506298	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085124	ATGGGGAAATTCTGG[C/T]ATAACTTAAACATTT	51317
rs570513181	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46060454	ACTCATATAAAATTA[C/T]GTTATATTATATAAA	51317
rs570528497	snp	C/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46060433	CAAGTTGTAATCTTA[C/G]CACATACTCATATAA	51317
rs570534639	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941942	CAGAGGATTAGTGTC[C/T]GGTAGGTTTTGTATT	51317
rs570567371	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059656	TCTCAAACTGGCCTC[A/G]AAGGATCCTTCTGCC	51317
rs570588523	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:46101487	AGGTACGTGGGGTTA[C/T]ATTATTCACTCTATT	51317
rs570594875	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933607	CTCCCTCCGCCCGTC[C/T]CTGCTCCCCACCCAA	51317
rs570614603	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45959039	AAACTGAATCCAAGA[C/G]CATATTAAAAGGATG	51317
rs570654769	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46017741	TAAAAACTGTTCTTG[A/C]TAAATATGTAGACTG	51317
rs570658680	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119360	GCCCGGACCTTCACT[C/T]AGATTTGAAATTCTA	51317
rs570659764	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933143	CTTCCTGGACACACA[C/T]ATCCTTCTTCCCTGC	51317
rs570662024	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46110687	ACAAATTGATGTCAT[A/G]TAAATAAAACAGCTT	51317
rs570671017	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46075886	CAACATAAAAATCAG[C/T]TATTGAGAACTATTT	51317
rs570702945	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46065718	GCCAGGACTAGAATT[C/T]ACTCCTTTTCTTTAA	51317
rs570713041	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45992427	CGCCTGTAGTCCCAG[A/C]TACTCGGGAGGCTGA	51317
rs570726255	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45937569	CACTGCAGCCTCCAC[C/T]TCCTGGGTTCAAGCG	51317
rs570741350	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049626	CCCACCTGTCACAGC[A/T]CTCTCCTTGCTGGTT	51317
rs570759319	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46026509	GGAGAGCATTGAGAC[G/T]TTTTCTCTTGTGGAA	51317
rs570776747	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46057675	AGGTCTCACAAGTGC[A/G]AAAGGTACTAGGCTG	51317
rs570784906	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939453	ATTAAGTCAGAAACA[A/C]ATTAAATTCATATGC	51317
rs570813755	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056838	AGTCAACAATACTCA[C/T]GCTGTCCTCCTCCCC	51317
rs570862219	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983565	TTAAATATAGATGAC[C/T]GCACTTAGAAACCAG	51317
rs570893162	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930298	CAGCTGTGTGTAACC[-/A]CCTCCATGCACGCTG	51317
rs570902801	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46041653	TCCATACATGAAGAC[C/G]CAGATTTAAAACAAA	51317
rs570903790	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001291	TGTGACCACCAGGGG[G/T]GCTGGAAATGGGGCT	51317
rs570916186	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46032823	ATCGCTTCATATTTA[C/T]TGGCCATTAATGATT	51317
rs570920977	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45936270	GTTGATACAGTGAGA[A/C]CTTGTCTCAAAAAAT	51317
rs570942420	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45992980	CTGTAGAGTAGAGGT[A/C]AGAAAACTGAAAACT	51317
rs570952032	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45956712	AAGCATGAAAATGAC[A/G]CACTAAGAAAAAAAT	51317
rs570964415	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015644	TTTTAAGTTTTCTAT[A/T]TTTAAATATTTAAAT	51317
rs570964888	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050130	AATGCTTCACGCCAA[A/G]TTTTAGAAAGAAGAG	51317
rs570996545	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930443	CCTAACTGCCTCCCT[A/G]TGTCAGGTACAACCA	51317
rs571001433	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46117091	TGTATTAATTAGTTA[A/C]CTATCTCAACAACTT	51317
rs571018059	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074704	GACGGGGTTTTGCCA[C/T]GTTGGCCAGGCTAGT	51317
rs571019636	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46117614	TATACCCCTTTCCAA[A/C]ATCTCAACTACTCTA	51317
rs571049939	in-del	-/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46117913	AATGGAATTTTTAAA[-/T]GGACTTACTCAAAAT	51317
rs571056484	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937465	AGGTTAAAAGTGAAA[C/T]GGGTGTTGTTTTATT	51317
rs571092363	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46061884	ATGTATGGGAGGTAA[A/G]TTTTGTGACCTTGCA	51317
rs571095490	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45948176	AAAAATTTCAGTACC[C/T]TGTTTATGAGCTCAA	51317
rs571148006	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:46032876	CAAGAGTATAAGTAC[-/AT]GTGTGAATGTACATA	51317
rs571154728	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957763	AAGCAAAAAAAAAAA[A/G]AAAAAAGAAAAAAGA	51317
rs571160797	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46107340	TCAGTTTCACCATCC[A/G]TAACATTAATTGAGC	51317
rs571171993	snp	C/G/T	7.37196e-05	0.00607084	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935731	ACTTCTGTTTCTCTT[C/G/T]TTCTTTTGCTAAAAA	51317
rs571185298	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46097322	CCACAGGCACTGAGT[A/G]ATTTGGGCCTCTGCC	51317
rs571203660	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045414	GCTGAGGGGAGTTGG[A/G]AAAGGTAGAGAAAGA	51317
rs571250747	snp	A/C	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46038558	GTTTATGATATAATA[A/C]CTGAAACTAGGTAAT	51317
rs571255786	in-del	-/TTCA			intron-variant	PHF21A	GRCh38.p7	11:45951071	GGAACGTTAAGACTC[-/TTCA]TTCAAGCCAGAGAGG	51317
rs571269206	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46012715	CTGCAACCCTACACC[C/T]ACATTTCTAATTCTA	51317
rs571299871	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46046140	TTTTGCTATTTTCAG[C/G]GTTTGTTTTCAAGAG	51317
rs571322508	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45979279	CCACCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC	51317
rs571360040	in-del	-/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46034228	TGCCCCCACCCCCCC[-/T]CTTGCATACTTTTCC	51317
rs571411362	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952435	TTTTGCAGAAACAAG[G/T]TCTCACTATGTTTGC	51317
rs571423603	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945027	CTCGGCCTCCCAAAG[C/T]GTTGGGATTACAGGC	51317
rs571428491	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46021736	TTTATTTTTTTGTAG[A/C]GATGAGATCCCACTT	51317
rs571431366	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46012678	GAGGTAAGTAAATCT[A/C]TATCTCTAGTGCTGG	51317
rs571433791	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006332	TAAATTCTTAATCTT[G/T]CGGTTGTATATACAA	51317
rs571438656	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028462	AATCTACTGCATTTT[A/G]AGGAAAAAAAGTTTT	51317
rs571439041	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113204	TGCATACTGGGACTT[A/G]TAGTAAGTAAACCAC	51317
rs571441086	snp	C/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46005404	ATATATTAACGCCTT[C/G]TATATACCAAATAAT	51317
rs571476802	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46091979	TGGAACATGCAGGCC[C/T]AGCTGTATTAGCAGA	51317
rs571485029	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45953455	TCATTCAGAGAGCAG[A/G]TGCCCCTCCTGGTAC	51317
rs571508471	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122639	TTTTATTAGTGAAAG[G/T]ATTTTATGCCTATTC	51317
rs571531999	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978257	AGTGAGCCAAGACTG[C/T]GCCACTGCACTCCAG	51317
rs571545752	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45944526	AGCCACAAAGCCCTG[C/T]GCAACTGGCCCAGCC	51317
rs571554211	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45994358	TATTTGTCTTTTGAA[A/G]TAGAGCTCAGATAAT	51317
rs571555818	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46004168	ATTTAAAAATGTTTA[A/T]ATTTATTTTCCATAG	51317
rs571563282	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46018976	AACACACACATCATG[C/T]AAGAAGCTAAAACTG	51317
rs571568035	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036147	TGACTGAATTTCGGA[G/T]ATGAGTGAAAGGGAA	51317
rs571585324	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45980240	GCAGAGCTCAGATGT[C/T]CTATTATTAACTTAG	51317
rs571595467	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46019992	TCTACATTTTGACTC[-/T]TTTTTTTTTTTAGCC	51317
rs571649440	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45969299	GTATGGTCATGCAGA[C/G]CTGCTCGGGCCTAGG	51317
rs571656864	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45977731	GGTGGTGATTAGGGT[A/G]AAAATTTATGTAGGC	51317
rs571665732	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087871	AGTGATCCTCCTGCC[C/T]TAGCATCTTGAGTAG	51317
rs571671733	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46095151	AAAGTGTTTCTTCTG[A/C]AGATTGAATATTAAT	51317
rs571675750	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45977206	GTGCAGTACGATCTC[G/T]GCTCACTGGAACCTC	51317
rs571682577	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46019474	AAGATGTGGCCAATC[C/T]AGGCAAAGCTGGCTA	51317
rs571708230	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46103542	ATGTTTTAGGAACAG[A/G]GACAAAATAAAATAT	51317
rs571713861	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044912	ATTCCATTCAAAAGA[C/T]AGGAACTGATCGAAG	51317
rs571723492	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961782	AGCCCCATTTTAGAG[A/C/T]GCTGGAGAGGACAAG	51317
rs571723965	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46078982	TTTCTAAACCCTTAT[A/G]ACCTGAAGATCAATG	51317
rs571730323	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46043269	CCAAGGACTTCTTTC[A/G]AAAGTTATCATGTCC	51317
rs571785788	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961172	CTTACATCTCCTCTT[C/T]GAACCCACGGTTGCT	51317
rs571795575	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102198	AAGTGATACACCAGC[C/T]TCGGCCTCCCACAGT	51317
rs571815159	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45977860	TTTTTTTTTTTTGGT[A/G]TTGAATGGCAGTACA	51317
rs571843164	in-del	-/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46110611	CCTTATATTTAGCCC[-/T]TTGTATTAACTCCTT	51317
rs571849308	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052058	GGTTGAGATGATCCA[A/G]GAGTAGCATATGACC	51317
rs571851661	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45948120	AGGGACACATTACCA[G/T]GTGGAGAAAAGGATC	51317
rs571859930	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112067	TTTCTGAAGTCAACC[A/G]AAGGCTTGTGGTATG	51317
rs571869854	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978777	TATCATTTCCAAATA[C/T]GCCCTTTTTGTGTAT	51317
rs571882152	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45934325	CTGCCCAGGGAGAAG[A/C]AGCTCTGCTGGCTGC	51317
rs571901588	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45987311	CAAAGACCCTAGACG[C/T]AGTAAATACCTAAGA	51317
rs571908682	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45941611	CCATAGAAATGAATA[C/T]AAAATGCCAAAACAT	51317
rs571930778	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005398	TGCACAATATATTAA[C/T]GCCTTGTATATACCA	51317
rs571932717	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006881	CAGGTACTAACAATA[C/T]GTATTTTCAAAGATC	51317
rs571952668	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935001	GTCACTTCACTCCAA[C/G]AAGGGTGACCTACTC	51317
rs571956380	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46114355	AAGTGCAATCTGCAT[C/G]AGGAGGCCTAACACA	51317
rs571991955	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094938	TTTAAACCTAAGGGA[A/T]CCCCATGAATGGGCT	51317
rs571995777	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059216	GCTAGGCATACAACA[A/G]TAAAAAACTGGGAAT	51317
rs571998300	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46102914	TAAGAGAAATAGAAA[C/T]AAAACAGTGGTGGCT	51317
rs572020484	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934827	TTTTGCCCTCAGCTT[C/T]CCACACCTGCTGGCT	51317
rs572041474	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45942503	AATCTTTGGCGCTAG[C/G]AAACAAGATTTCTGA	51317
rs572043181	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123257	TCTATTACCTTGTTA[G/T]GTATTTTCACAAGAG	51317
rs572050173	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985984	ATTCTCTGCATGGAT[A/G]TTTAACAGATGGCAA	51317
rs572055462	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46043985	TTGTAGTAAATCAAA[C/T]AAACTGAGGAAAGGT	51317
rs572064145	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46076131	CAGGCACTGCCTGAA[C/T]TGGTAAAGTGGAGGT	51317
rs572083580	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087383	TACTTTCTCCATCAG[A/C]TTGTTGTCTGCTTCT	51317
rs572143646	in-del	-/TTC	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46044738	AAAAAAAAATCTGCT[-/TTC]TTAACTATATGCCTG	51317
rs572155929	in-del	-/AAAT	0.00517822	0.0506191	intron-variant	PHF21A	GRCh38.p7	11:46111475	GCAAGACTCCGTCTC[-/AAAT]AAATAAATAAATAAA	51317
rs572169383	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949674	ACTCTCACCTGCAAG[A/T]CCACGCTGTCCTACA	51317
rs572194721	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059803	TCAATCTCGGCTCAC[G/T]GCAACTTCTGCCTCC	51317
rs572199632	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46037387	TGGCTCATGCCTGTG[A/G]TCCCAGCACTTTGGG	51317
rs572218587	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036257	ACAGTCATAAGTAAC[A/G]TAACTGGAAACACTG	51317
rs572220269	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076672	ACACATGAGGAAAAA[C/T]AGCAGTTCTCTTAGA	51317
rs572222857	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46016084	AGGTTTGTTTACACC[A/G]GCATCACCACAAACA	51317
rs572240947	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120073	GCAGAAGAAGAAGAA[G/T]AAGCGGAATTTCCCC	51317
rs572278261	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46082753	AAAATTGGTATGCTT[C/G]AATTCAGAATATGAA	51317
rs572278349	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46002547	AAAGGAATTCACACA[C/T]GGCCTTTTTCATTTA	51317
rs572295752	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46013579	AAGTAGACACAGTCA[C/T]GTGTTGCTTAATAAC	51317
rs572308135	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46051528	ATGGGTTGAAATTGC[C/G]TAAGGAAACCTCAAA	51317
rs572319221	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46104489	CTCTGTTAAAACTGA[C/T]ATATTCCCATGTATT	51317
rs572359727	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46003982	CTCAGAACAAAAATG[C/T]TTCAATATATTAAGT	51317
rs572365386	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46034287	TTCATAAGAACTCTT[C/T]ATATGTAAGACTAAT	51317
rs572387875	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967738	CCAAGTGTGGCCCAT[G/T]AAAGTCTTGTCGGTA	51317
rs572396691	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46047456	TAGGAAATATTCCTG[C/G]CTTGTTCTTCTGGAT	51317
rs572406217	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46031399	TCACTTCCTTGGATA[A/C]ACAACAACAAAGAAT	51317
rs572411480	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45960165	GTATGACCCAGCAAT[C/T]TCTACTCCTAGGTAT	51317
rs572427596	snp	G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46025821	TAAGACAGAGTCATC[G/T]GCAGATATGTGATGG	51317
rs572441557	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085385	TCTGTTAATATGACA[C/T]CCAGCTTGACCTTCC	51317
rs572454126	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46033082	ATAATGTTTTATTAG[A/T]TTTTATGTATCCTGT	51317
rs572509715	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46092220	CCTTCAGCTCTCTAG[A/C]CCCCTATAACAGAAG	51317
rs572522226	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45959415	ATTTCCTTGACTTTA[C/T]AAAAAACATTTATGA	51317
rs572536718	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46018105	AATACAAAAAATTAG[C/T]CGGGCGTAGTGGCGG	51317
rs572546952	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45937642	CCTGCCACCATGCCC[A/G]GCTAATTTTTATATT	51317
rs572593216	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46022659	TAGAGACAAGGTCTC[A/C]CTATGTTACCCAGGC	51317
rs572600724	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45957731	CACCTTAAGAAACAG[-/A]AAAAGAACTAAATTC	51317
rs572606874	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933329	AGAAGAACCTACTGG[C/T]TGTTCTTGGTGTCAG	51317
rs572612173	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46024932	CTATAAAGCCATCAT[C/T]CCTTATTATTGAACA	51317
rs572621918	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46063776	CAGCTATTAGCAGGA[A/G]CTGATGAGGCTTAGG	51317
rs572626788	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084686	AGAATCATAATTTTT[C/T]TTTTTTTTTTTGAGA	51317
rs572632522	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45973670	GTAGTGTAACAGCAA[A/G]GACTGACTGCATTAT	51317
rs572641095	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101726	TCGCAGCCTCGACCT[A/G]CCAGGCTTAATCAAT	51317
rs572641708	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45992756	AAGACACAGGGAAAC[A/C]CACAACTATATACAA	51317
rs572680611	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46101111	CACAGACAGGAAAGT[A/G]TACATAAAATAAAAT	51317
rs572716786	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45969706	GAATGTTTAGCTAAG[C/T]GGGATAGACAGCTGG	51317
rs572720018	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45939174	GGAGAGGTCTATAGT[C/T]GCCAAGGCCAAAATT	51317
rs572733008	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45963934	CTGGGCGTGGTGGCT[C/T]ATGCCTGTAATCCCA	51317
rs572762941	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46030385	TTACCAAATGATTTG[C/T]CCAGGTTTTCATCAT	51317
rs572775576	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022359	ACTCAGGATGCTGAG[A/G]TAGGAGGATCACTTT	51317
rs572799734	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46056471	TTAGTATGAGCTAAT[A/G]TCACAGTGAAGATTT	51317
rs572841291	snp	G/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45963008	AAAAGCTCTATCAAC[G/T]TGAAGGCCACGACAG	51317
rs572850666	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46038777	ATAAAACCACTAGTT[C/T]CACTCCCATGATAAC	51317
rs572850771	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46029795	ATAACAAATGTCCGT[C/T]AGAGTGCTTTTAGTT	51317
rs572853591	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45955828	CCAGGTGTGAGGAAC[A/G]GAACCTCCAGCCAAC	51317
rs572873174	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46006590	CTGCCTGAGCTAGAG[A/G]ATGAAGTTATGCCTT	51317
rs572884197	in-del	-/C	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45984780	TGGATGTCAGTGCTG[-/C]CAAGTCTCTGCTTTT	51317
rs572890126	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015023	ATAAAAAAAAATAAA[A/T]AAATAAAAAATAGTT	51317
rs572910282	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46005750	AATATTTGTAGCACA[A/G]TTAAGCTTCCATAGC	51317
rs572920106	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45972679	AGCACTTTGGGAGGC[C/T]GATGCGGGTGGATTG	51317
rs572934818	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46061898	AGTTTTGTGACCTTG[C/T]ATGTCTTAAAATGTC	51317
rs572952231	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46043364	GACACAGGTTACTTC[G/T]GTTTACCCACATCAT	51317
rs572953522	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46089027	CATTTCTTTAACTAA[C/T]GATAAGTCCATGACA	51317
rs572962957	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930111	AATAAGAAGGACCAC[A/G]CCCTATAAGAGAATG	51317
rs572997942	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45988826	AACTCAGGAGGTGGA[A/G]GTTGCAGTGAGCCAT	51317
rs573014682	snp	A/C/G	0.00795819	0.0626103	intron-variant	PHF21A	GRCh38.p7	11:46069292	GGCAATAAACTCAAC[A/C/G]AACAATTGGACCAAT	51317
rs573015222	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45946449	AGTGCTGTGGCACGA[C/T]CTCGGCTCACTGCAA	51317
rs573043429	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45979611	TACAAGTGATACTTA[C/T]CTGGGTTATACTGTA	51317
rs573054818	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021573	GTTCAGAGACAGGGT[A/C]TCACCCTGTCATCCA	51317
rs573067264	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45960185	CTCCTAGGTATATAC[C/T]CTAAAGAACTGAAAA	51317
rs573069498	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45957423	TAGAAAGACTAGAAT[A/C]ACATAAAATCTCTTC	51317
rs573071095	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080186	TTTTTTGAGACAGGG[C/T]CTTGCTCTGTCACCT	51317
rs573152258	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45994580	CCACAGGCCTAATGT[A/G]TGTGATGCTGAATTT	51317
rs573180294	snp	A/G	0.0142736	0.0832652	intron-variant	PHF21A	GRCh38.p7	11:46011690	CCGCAGAATACAGAT[A/G]TTCTTTCAAGCAATG	51317
rs573182865	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46053541	CTTCATTATATATAT[A/G]ATTATATGTATACCA	51317
rs573201457	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46113488	AAATAGTTTTTTAAA[A/G]TTTGAATGGATCCAT	51317
rs573227692	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46045503	GTCTAATTACTTGCT[A/T]TATTTTACCCAAGTA	51317
rs573231763	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45949096	GCTCAAGGGTTTTAT[G/T]GTATGTACTTGGCTC	51317
rs573239570	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998343	GGATGTTAGGGCCAT[C/G]GATAGAGTGGTAGGC	51317
rs573248766	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104686	CAATAATAATGATAA[A/G]AGCAGCTATCATGAT	51317
rs573253584	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46080088	TTTGTCACTCTCTTT[C/T]GGTGACAAGGCACTT	51317
rs573260323	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46054364	GTCCCCAGATGATTC[A/G]GGAATAAAAATGCTA	51317
rs573260889	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929564	GACCTCTGGCCTGCC[C/T]GTCCCATCCCGCCTG	51317
rs573269970	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45981346	AGCCAAGATCATGCC[A/G]TTGCACTCTGCACTC	51317
rs573273368	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944672	GCTGTTCCCTCTGCC[C/T]GGCAGGCTCTTCCCC	51317
rs573295638	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045120	GCCTTAGCTTGTGTG[A/C]TTCCCCTGACTTAGA	51317
rs573312641	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46079227	TCCCTATGGCTAATC[A/G]GGTTTGGACCAAAAA	51317
rs573349423	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45936762	TAGGAGAATCAAGTT[C/T]AAGGCAGGAAGAGCC	51317
rs573362286	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45953923	TATAGAAATACGGTA[C/T]AGGTTGTCCTTTCTG	51317
rs573369108	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961277	ATCAAGTATACTTTA[C/T]ATACTTGTCTGCATG	51317
rs573369554	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46090868	ACACTAAGCTTGTGG[C/G]AGTTATTTATATCCT	51317
rs573379621	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46028730	AGGCGCCCGCCACCA[C/T]GCCCAGCTAATTTCT	51317
rs573394699	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46054477	TTTTTATGCCTGGGC[A/G]CCATTCTCGAAGATT	51317
rs573408003	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019712	GTCGTATTAGTCTCC[A/G]GTTAGATTTAACTGG	51317
rs573411441	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45945325	AGGGCTACTAAGTAT[C/T]TGACAGTTTTTCCGG	51317
rs573414671	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952810	AATTACTGGCCAAAT[A/G]AAATCTGTCAGATAT	51317
rs573493703	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46020551	TTTCTGCTTCCCTTG[C/T]GTCTAACACCATCTG	51317
rs573501381	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45951918	TTCAAGCTATTCTCC[A/G]GCCTCAGCCTCCCGA	51317
rs573509675	in-del	-/A	0.40853	0.193309	intron-variant	PHF21A	GRCh38.p7	11:46096288	TAAAAAATAATAATT[-/A]AAAAAAAAAAACCCT	51317
rs573513402	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46019333	ATGTCAAATGAATCA[C/T]CTTAATTTTTTTCAC	51317
rs573567980	snp	A/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46029740	CTAAAAACCTAGCAA[A/T]AAATTTCATGTCATT	51317
rs573592653	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46096502	AATCCAACAGAAAAT[-/A]AGTCTTCACTTCCTT	51317
rs573628970	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970907	AGATAATGCACTGAA[C/T]TTAGTCCTTGGTGTC	51317
rs573633684	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45981877	AATCTTTAAGTAAAA[A/T]AAAAAGTTCTCTTGA	51317
rs573638102	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045475	ATGTTTTTAGGACAC[C/T]ACTATTACTCCAGTC	51317
rs573663195	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46012870	TACTTCATCACATCC[C/G]CCCAACTCTTTACAT	51317
rs573668022	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46022298	ATTTCTACAAAAAAA[G/T]TTAAAAATTAGCCAG	51317
rs573674039	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46016921	AACATGATGTGCCCT[A/G]ATGTGATGAAGTCAC	51317
rs573677029	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45962825	ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	51317
rs573727895	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45979462	TACCTCCAAAAATTC[A/C]AAATAAGGTTTTAAT	51317
rs573735850	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45977695	GTCAGTTTTGAATGC[C/T]TAATTTCCAAATAGC	51317
rs573746492	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45935834	GCCAAAGAAGGTATT[A/T]TCCCCAGAGCTCCCA	51317
rs573748427	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46096685	TTAAAATGTGGAACT[A/G]TCCCAGGACTCAGTT	51317
rs573795023	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45996725	TAGGATCCCAATTAT[C/T]TGGGAAACAAAAGGT	51317
rs573798252	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45974217	ATTTACTATTTATTG[A/C]CACCAAGACCCAGGT	51317
rs573805648	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46038310	TTTTTGTATTTTTAG[C/T]AGATACGGGGTTTCA	51317
rs573806588	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46021470	TTCATCCTGGGCCCA[A/G]GCATCACCAAGGGTG	51317
rs573808100	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052737	CCTCTGAAATCTTTA[C/T]CAAAGCAGTTAATCA	51317
rs573828657	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975141	CAACATAGTGAAACT[C/T]CACCTCTACAAAAAA	51317
rs573831750	snp	A/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45956281	TATAAAAGCCAGTGT[A/T]ATTATTTATTTTTAA	51317
rs573839251	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45957292	CAATTAGACCTGTCA[A/G]GCATAGAAAGAATAC	51317
rs573849177	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105350	AGTGCTTTCCAAGCA[C/T]GTGTGCCAGACGTCT	51317
rs573865421	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46086359	CTCCTGACCTCGTGA[G/T]CCGCCCGTCCTGGCC	51317
rs573874955	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45987123	CAGTGGCTCATGCCT[C/G]TAGTCCCAGCTACTT	51317
rs573884045	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46104582	ACTCTTTCTCACCAC[A/G]CATTTCAAGGGAGAA	51317
rs573942015	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46004671	GCATAGCACAGACTA[C/T]TACTTTTTCATAGCA	51317
rs573949750	snp	C/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932063	GCAAGACAGAGCGAA[C/G]GCCACGCTGGGGCTC	51317
rs573976320	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46061100	TTTTCGTCAGGTTTG[C/T]CAAAGATCAGGTAGC	51317
rs573994088	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978612	GTAAGAGGTATCCAC[A/G]CTTAGGTTTCAGAGG	51317
rs573998145	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45988698	GTTCGAGACCAGCCT[C/G]GCCAACATGGCAAAA	51317
rs574004761	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944539	TGCGCAACTGGCCCA[A/G]CCACTTCTGAGGCCT	51317
rs574013371	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122154	CCCCCTCCCGCCGGC[A/G]GGAGCTGCAAAGGGG	51317
rs574014007	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45948761	ATTCTCAGAGAACAA[A/C]AACAAAACTATTTTC	51317
rs574015270	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46069824	TTCTAAGCTTCTTAG[A/C]AAAGTAGTACTTTAC	51317
rs574026997	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46005502	TATTAACTTAATTAA[C/T]GGGCACCAAATGTTC	51317
rs574041113	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46115558	AGCAAAAACATACAC[A/C]TGAGAAAATTAATGT	51317
rs574056330	snp	C/T	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45995748	ACGCAGCTCTGTTAC[C/T]TATTGGCACACATAT	51317
rs574062198	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46062020	TCCAATGACTGCTAG[C/T]TTTCTTTGTTGCTGC	51317
rs574063409	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009675	AACATTCCAAAAGTA[C/G]CAAATAGCAGAGCCA	51317
rs574095278	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943764	GGTGGAAAAATCTGA[C/T]AGAAACTATCTTAGG	51317
rs574098303	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009000	TTTTTTTTTGGAGAC[A/G]GAGTCTCACTGTCGC	51317
rs574115910	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45977841	TTTTTTTTCTTCTTC[C/T]TCTTTTTTTTTTTTT	51317
rs574158965	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46118590	TAACTGTACACAAAA[C/T]TTCCTCTTTGCCATG	51317
rs574174131	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46103876	CTGGTTTCACTTATA[A/G]GATAGAGACATTCGT	51317
rs574174619	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46099346	GATAGCCAAGAATAA[C/T]CAGAGTACTTCCAGA	51317
rs574189166	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094091	AATATATAAAATATG[C/T]TGAAATTCAAAGTGA	51317
rs574197117	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45952557	ATTTCACAAGTTCCT[C/T]AGCAATTTTTGTGAC	51317
rs574197924	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46095048	GGTCCACGGCTTTAA[A/T]TGGTTTCACAATGAG	51317
rs574213884	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46112666	TATTCAAGATGTTGA[C/G]AATTATTACAGAAGA	51317
rs574238167	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076989	ATCACCTAATGCACA[G/T]ATCCTAAATACAGGC	51317
rs574244461	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46087044	ATAATAATACTCTGA[A/G]CTGTCTAGAATTTGT	51317
rs574272942	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45992231	GAAAGTGGAATTAGA[C/T]ATTACTTAGAAAATT	51317
rs574282979	snp	C/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:46027634	AAGATCTTTAAAATA[C/G]CCAAGTGCTAAAGAC	51317
rs574325450	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46086427	CCCAGCCAGCTATTA[A/T]CTTTTAAAATATTTG	51317
rs574382153	in-del	-/AGGAAAGGAAAGGAAAG	0.00874735	0.0655527	intron-variant	PHF21A	GRCh38.p7	11:46079835	CCCAAACAAATGGAA[-/AGGAAAGGAAAGGAAAG]AGGAAAGGAAAGGAA	51317
rs574382447	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46016053	TGCTATAGTTTTATA[C/T]GACTGGCAGCACAGT	51317
rs574385605	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45961180	TCCTCTTCGAACCCA[C/T]GGTTGCTGGAATTTG	51317
rs574409693	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960459	ATCACATATTGTATG[A/T]TTCTATGTATATGAA	51317
rs574420615	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015371	AATGTCAATTTTTGT[C/T]TTTGTTACAATTACT	51317
rs574421119	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932268	TGGCTGAAAGACCAA[A/G]AGCAGCACCAAAGGA	51317
rs574438017	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46049790	ACCCATTAGAGTCAC[A/G]AATAGCAAACTGCTG	51317
rs574443328	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46063103	CTATAAGAGAGAAGT[C/G]GGGAGAGGAATAGAG	51317
rs574452495	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46001532	CAACAGACCACCTAA[C/T]AACATAGGGAGGAAA	51317
rs574459424	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46049099	CCAAGTTTTAGAAAG[C/G]AGAGATTATCATTGT	51317
rs574459996	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46099460	CCTCACTTCTCAATA[C/T]AGCACTGCTGTACTC	51317
rs574464078	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45981172	GGGTGGATCACTTGA[C/G]GTCAGGAGTTCAAGA	51317
rs574475057	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067075	TGTATTCTTTACTAA[C/T]GCACCTTATGTATTA	51317
rs574475425	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058105	ATCTCACTTAAACCT[A/G]CAGAAAACAGAAACT	51317
rs574525296	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45965729	TAATGTTCATTTTGG[G/T]ACATTAATTCTATAG	51317
rs574526488	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46083516	ATTGTTACAAATTCA[A/G]AAGTAGTCAATGCAT	51317
rs574533145	snp	A/C	6.62815e-05	0.00575642	intron-variant	PHF21A	GRCh38.p7	11:45965286	ACGACAAGGCTACTG[A/C]CCAGAGCAGGTACAT	51317
rs574533658	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990088	AAATTACAAAATCTA[A/G]TTACAAAATCTAATC	51317
rs574542741	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46067897	AGTACCATGAGTACA[C/G]AGAAGAGGAGTGTCT	51317
rs574556613	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45940407	CACCATGTTGGTCAG[C/G]CTGGTCTCGAACTCC	51317
rs574561767	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023229	GCAGTTTAAGTGTAA[C/G]CAATGGTTTCTTAGC	51317
rs574577949	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46008148	TTAACATTTCAGCAC[C/T]TTCCCCTACAATGTG	51317
rs574594248	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45973430	TTTTCTGCCTTATGC[A/G]CATATACACATATTA	51317
rs574608208	in-del	-/CA	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932414	GCACCAAGAAGAGAG[-/CA]CACGGTCTTTTCTGA	51317
rs574616703	in-del	-/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45955047	TACTGTGGCAACCAG[-/T]TGCTCTGGGGCACAA	51317
rs574636460	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46073372	ATTAGAGTGGTTCAT[A/G]TATTTAATACCATGA	51317
rs574690751	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45954784	TGTGGAAGTAATGCT[C/T]CTTTCATATGGCAAC	51317
rs574702846	snp	G/T	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:46023894	CCAGGAGGCGGAGGT[G/T]GCAGTGAGCCAAGAT	51317
rs574719468	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46072654	AAAGTATGGTTCAAT[A/G]TGAGATAATAATAGA	51317
rs574728734	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45990855	CACATAGCAGAACAT[C/T]TGTTACAATCGAACC	51317
rs574748626	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930834	AAGAGCAGCGGAGGG[A/G]AGGAGGAGGAAGCAA	51317
rs574767839	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45938607	ATATGTTTTTCTATA[C/T]ACACAGACCCACAAT	51317
rs574769859	in-del	-/TGGC	0.0126979	0.078662	intron-variant	PHF21A	GRCh38.p7	11:45989728	TTTAGCTGGGCACAG[-/TGGC]TGGCTCATGCCTATA	51317
rs574773457	in-del	-/A	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46002865	AGAACAAAGCAAAAC[-/A]AAAAAAACACCCAAT	51317
rs574777867	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098610	GTCTAATGATCATAA[C/T]GAAAACTTCTTAATT	51317
rs574781117	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46106682	TAACATGCATGCTGC[A/G]TACTCCACAATGTTA	51317
rs574819171	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46090744	AATGTGGTATTCAAT[A/G]TGTACCTGAATAACA	51317
rs574827404	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45946365	GCCCAGTGGGAGCCA[G/T]GGCCAGGAATGAGTT	51317
rs574855899	snp	C/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45960372	CAGCCATTTAAAATA[C/G]AAGGGGGCACTGATA	51317
rs574857070	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46059179	CGTACAAATATTTAC[A/G]TCCAAGGATGTACAC	51317
rs574857100	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46097195	GGTATATTCTCTCGC[A/G]AGCCAGAGTAAGCTT	51317
rs574861110	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46047787	TCTGCATGGTGAGGT[C/G]CAGTGGGGATCAAAT	51317
rs574873209	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46039028	AGAGAACAGCAAGGA[A/G]CCCAAAATTACTGGA	51317
rs574896703	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46015090	GATTTGCATTTCTTT[A/G]ATGATTAGCAATGTT	51317
rs574902774	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46007293	CTTTACAGAAGATAC[C/T]TCCATCTACCTTTTT	51317
rs574907550	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931187	CCTAGCCCCGTCCTC[C/T]GACCCAAGACTCCTA	51317
rs574921467	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45991114	CTTTCCAGAATGTCA[C/T]AGAGTTGGAGTCATA	51317
rs574923110	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46063740	AATACTAGAAATTTA[A/G]AGAGTTATATATAAT	51317
rs574958971	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46048221	CTCCAGGGAGGTGCA[C/T]ATTCTAAACATTTTT	51317
rs574993810	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45992055	CTAGGCATGATAGGG[A/C]CTGACATCAACTGGA	51317
rs575002343	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45937983	AATATGGCAGAGGGC[C/T]TCTGAGGGAATGAAG	51317
rs575003144	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46062864	ACAAAGACTTGGACA[A/T]GAATGTTCAAATTAA	51317
rs575012278	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998953	TCAGCCTCCCTCCCG[A/G]ATAGCTGGGATTACA	51317
rs575026048	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040238	AACAGAGTTTCATTA[A/C]ACATAATGGTCTCAC	51317
rs575032799	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055291	TGGATTTCATGAAAA[C/T]AACTTGGTTTTTTAA	51317
rs575051775	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46056035	TCTTTATAGCTCAAG[C/T]AATACTTTCTCAATG	51317
rs575059187	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46115317	TGAATTGAGGGACAA[A/G]TAATAGAAAAGTTAT	51317
rs575076444	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46076016	CACTCTTTCTAACCA[C/G]AGGGAGAGTGGTGGG	51317
rs575077171	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46102477	ACAAATCAAGGAAAG[A/G]AAGCCTAGTCTTCTC	51317
rs575095273	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46008056	CTACCCACCAACTGG[G/T]AGGTGAAAATTAACA	51317
rs575160333	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46046813	GAGTGTCTGGACAAA[C/T]GAGAGTAGTTTCCAA	51317
rs575178611	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023047	TGAGCCACCGCGCCC[A/G]GCCTTGTTATTTTCT	51317
rs575207075	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45998818	AGCCACCACACCCGG[C/T]CTTTTTTTGTTTTTG	51317
rs575209091	snp	A/G	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:45988997	ATATTTGTTACAATC[A/G]CTTAAAGAAAAAAAT	51317
rs575244033	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46062614	GCCTGTTCTGACTTG[A/C]ACATTAGCAGCTTCC	51317
rs575251342	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45948442	TACCTCTTTCCTTCC[C/T]GGAAAGTCTGCAGCT	51317
rs575306514	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46065911	AGAGCAAGGAGCTAC[G/T]GGCTCACAGAAGAGA	51317
rs575352962	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46015750	CACAATCATCAATAT[C/T]ACTGTCTTTTACCTC	51317
rs575368798	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46040618	ACCAAAAATAACAGT[A/G]TGTGCTGAAGGACTG	51317
rs575386158	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45999546	CAAATGTACTTCAAA[A/C]TGCAAGCTTATTTTG	51317
rs575402558	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107805	CTTTAGTATGTCTTT[C/T]TAAATATAATGCCAG	51317
rs575429389	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45956817	GCGTAAGTCCCTCCT[C/T]ACCAGTAATCACTTA	51317
rs575441721	snp	A/T	0.00478085	0.0486577	intron-variant	PHF21A	GRCh38.p7	11:46116578	CTTTTTTTTTTTTTT[A/T]AATTATGAGAAACTG	51317
rs575476209	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45961990	GTTGGTTATGTCTGA[C/G]AGGGGAAGGACACGT	51317
rs575485017	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46014464	TGTGAATAGTGTGGC[A/G]ATGAACATACAAGTG	51317
rs575574779	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46045763	GAAGCCCTACTCTTG[C/T]CTTCTGTGAGTTTCT	51317
rs575584496	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994498	CTCCTCCACGTATCA[A/G]GCAAGACCAGGGCTC	51317
rs575601486	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46105713	GAGAAAAAAGCAAAA[C/T]TCTCATAATTTTGTA	51317
rs575631197	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46098570	ATTCACAAGCTTCCA[C/T]AGCTCTCACGAAGCT	51317
rs575633405	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45984770	CCCTCCACAACTGGA[A/T]GTCAGTGCTGCAAGT	51317
rs575634713	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46082243	TTTCTATCCAGTAAG[C/T]TCAATTTCAGCCCTA	51317
rs575637982	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46111561	AACAATATTGTAAGA[A/G]CTCCTCGCAAGAGAA	51317
rs575670640	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45993816	AGTGATGCTGGGAAA[C/T]GGGACGGTCAGAGAT	51317
rs575688055	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46091436	AACCTCTCAAAGTAG[A/G]TATTAGGAAAAAATG	51317
rs575691946	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46055230	AAATATAACAAAGCA[A/G]CAAATTTTTAGTAAT	51317
rs575698070	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45936951	CTTGACCTGACATGG[A/G]CTGCCTGTCTCAATT	51317
rs575721146	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46023046	ATGAGCCACCGCGCC[C/T]GGCCTTGTTATTTTC	51317
rs575728217	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:45953708	TTTAATAGTAGTAGT[A/C]AAGAAGAAAGAAGAC	51317
rs575743577	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46071793	TTTAAAAAATCATGA[A/T]ATAGCCAATTATGCT	51317
rs575745235	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45985916	GTACAAATAAACAAA[C/T]TGACAACAGCAGCAA	51317
rs575753684	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46059011	TGCCCCAGGGTCACC[C/T]AAGATGCCCTAATAC	51317
rs575775285	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45953066	CATTTGGGGTTTGGG[A/G]TTCTAATGTAATACA	51317
rs575799679	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45945339	TTTGACAGTTTTTCC[A/G]GAACCTGTTTCTGAT	51317
rs575803435	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:45938693	ACAGAACAATTATAA[C/T]GATATACTGTAATAA	51317
rs575812911	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949253	AGTGACTAATAAAAA[C/T]GATAAGTCAAAAAAA	51317
rs575816880	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013112	AACTTATTTAAACCC[A/G]GTTAAACTGGGTATT	51317
rs575836205	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930209	CCCAAGAGAGAAGTA[C/T]CAGAGGTGGCTGGAG	51317
rs575850492	snp	A/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46046610	AATCATTTTGTGCAT[A/G]TATTTCCCTCATATA	51317
rs575865434	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45953836	TAAATTGCATGGCTA[C/G]AGTAAATATGAATCT	51317
rs575883754	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46013642	CATTTCATTGCTGTG[A/C]GAACATCATACAATG	51317
rs575889317	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120018	GGGAGGGCCGGCCCC[A/G]GGGTGAGGGGTGCAG	51317
rs575906381	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45944729	TTCATAAACATCAGC[A/C]TCCTGCCAGTATGCT	51317
rs575924838	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110942	AGGCACCTGCCACCA[C/T]GCCCAGCTAATTTTC	51317
rs575928379	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46005946	TAAGAAAAATAAAAC[A/T]TACAATTTTAAAAGT	51317
rs575930724	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46021414	AACTATTAACAAGTA[C/T]ACACCATACCTCCAT	51317
rs575943036	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45945343	ACAGTTTTTCCGGAA[C/G]CTGTTTCTGATCAAC	51317
rs575954129	snp	A/G	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46101899	GAGTCTCGCTCTGTC[A/G]CCAGGCTGGAAGCAG	51317
rs575979251	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46054474	ATCTTTTTATGCCTG[A/G]GCGCCATTCTCGAAG	51317
rs575993818	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966393	ATGATTCCTACCCCA[C/T]CCTCTACTCTCTAAA	51317
rs575994879	snp	A/C	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46003146	TAGAATAATTTCCTC[A/C]ATAGAATCTTTTTAA	51317
rs576048171	snp	C/G/T			intron-variant	PHF21A	GRCh38.p7	11:46094028	GGTAAACCACAGAAT[C/G/T]GGAGGTGATAATTAT	51317
rs576067970	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094488	ACTTTCTCTTAACCC[A/G]CTGCAGGAGTTACTC	51317
rs576075151	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46083914	GATTTCTTTCTTTTT[A/T]GTTAACACCTTTGGT	51317
rs576076718	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46073214	GCGCCTGTAGTCCCA[A/G]CTACTTGGGAGGCTG	51317
rs576084825	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46042779	TTTCCCCTTCTGCCA[C/T]AGATAGCACCTTCTT	51317
rs576086040	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45934384	CTCAGTGGAGTGGGC[A/G]GCTACCACCTAAGGA	51317
rs576087165	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46111114	AAATCACAACTATGT[-/G]GGGGGGGGAGGCTAG	51317
rs576095963	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46034674	TATGGCTGTGCTACT[C/T]GCCTCCTTTCCTGGG	51317
rs576106940	snp	C/G	0.00157169	0.0279888	intron-variant	PHF21A	GRCh38.p7	11:45935565	GGGCCCACACGTACT[C/G]TTACGTATATTGGAA	51317
rs576151315	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46010538	GTTTGGGAATAGTGG[C/T]ATGAATAACTCAAAA	51317
rs576157079	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058339	TGTCACATTGTTGGT[A/G]AAACGAAACCTGATT	51317
rs576157310	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46009757	ACTGCACAATACAAT[A/T]AATATAATTCTGCTC	51317
rs576191922	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067281	AAGAAACGACACAGC[A/G]TAACAAGTATCTGAA	51317
rs576194857	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46024851	TCTTTAAGAATAAAC[C/G]TGCCATCCTGATGAT	51317
rs576202965	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45967457	CCCTAAGTGGGGTGA[C/G]TCTCATAACTTGGGC	51317
rs576289559	in-del	-/A	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46113438	AAATGCTGAAAAAGC[-/A]AAAAAAACTTGATGA	51317
rs576294319	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933230	ATAACCACGGAGATG[A/C]GCGACTCACCAAGCA	51317
rs576349043	snp	C/T	0	0	intron-variant	PHF21A	GRCh38.p7	11:45975214	AACTACTTGAGAGGC[C/T]GAGGTGGAAGGATCA	51317
rs576355672	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932190	CGGCCAGGGTGCGTG[A/C]GCACCACAGAGCTCC	51317
rs576357122	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46033103	TGTATCCTGTGACTT[C/G]TATTTTTTCCCAAGT	51317
rs576377533	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46050463	AGGGAGGCAAATTCC[A/C]TAGCTGCCGAATCAC	51317
rs576389839	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46069354	AACTAGACTAAATCT[C/T]AGGAAATTCCTAGGC	51317
rs576401913	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032924	TATACATACATGTAC[A/G]TATAATCTCTAATAA	51317
rs576471086	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119212	CTAACTTTCCCAGCT[C/G]GAGCATCTACATTCC	51317
rs576475672	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45997616	TTTCTTTCACTAAAT[A/G]CTTGTTTTGCAGCCT	51317
rs576519146	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933037	ACACACCTGGGTCGC[A/G]TGCTGCTTCACTCAA	51317
rs576530724	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45983700	AGCTGGCTTTTCTAA[C/G]TCTCACAATCCAGTC	51317
rs576531456	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100294	AAAATCCCATGAGCA[C/T]GGACTTTTTTCCTAA	51317
rs576567075	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45939669	ACCACCCCCATCACA[C/G]TGATAGTGTTAGGAC	51317
rs576589021	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46000329	AGAAGCTAAGCACTA[C/T]TTCTTCATACTCTAC	51317
rs576602271	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46025621	AAAAAATTTTCACTT[C/T]GACACAATTTCAGGG	51317
rs576608550	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45966791	CGCCCAGCTAATTTT[C/G]TATTTTTAGTACGGA	51317
rs576615241	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032143	AGAGCAATGTCCTGT[A/G]TCCTTAGTTAGGATC	51317
rs576629434	snp	A/G	0	0	intron-variant	PHF21A	GRCh38.p7	11:46041763	ATAAATCAGATACCT[A/G]TATACCCTTCCACGC	51317
rs576656403	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46100928	TCCCTCCTTGACAAA[C/T]CATTTTATAAGTGAA	51317
rs576679413	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46118215	CCAGGTAGGTGTCTT[C/T]TTCATCTATTACTAC	51317
rs576684526	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45991627	AAAAATAAGTAGAGA[C/G]GCAGTATTGTGCTGT	51317
rs576717092	snp	C/G	0	0	intron-variant	PHF21A	GRCh38.p7	11:46108703	TAACTTAGATGCACA[C/G]CTTTTGTAATATTTC	51317
rs576726423	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46062544	AATATCTTCTTTTAC[A/G]GATCTAGGGATCTAA	51317
rs576744356	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110896	GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCCCG	51317
rs576747946	snp	A/G	0.00318978	0.0398085	intron-variant	PHF21A	GRCh38.p7	11:45990995	TATACTATCACACAG[A/G]GTAGTTTCACTGTCC	51317
rs576756906	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46049935	CTTATTTTAATTTTG[C/T]ATATTTGTCAGACCT	51317
rs576763527	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46009120	GCTGGGATTACAGGC[A/G]TGCATCACCATGCCC	51317
rs576773328	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46110018	GGTCTATTGGGAGCA[A/G]GGTGGATCACTAATT	51317
rs576785699	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46091572	AGCTAACTAATCCAA[A/T]ATTAATTTTAAGAAT	51317
rs576837086	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932022	AGGCAGAGAAAGGAG[C/T]GGGAGCTTCAGACCT	51317
rs576849888	snp	A/C			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932672	CTTAATTTAAGTAAC[A/C]CTAGGAAGACCTCAA	51317
rs576874052	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46090961	AATGGGTTAAGGTCG[C/T]TTCTCTAAGATTCCA	51317
rs576879863	snp	A/T			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929436	AACAAACAAAAACAA[A/T]AACTTTGAAGCACAA	51317
rs576930820	snp	C/G	0.00914312	0.0669923	intron-variant	PHF21A	GRCh38.p7	11:46074463	GCTCTTTTGGCGGGA[C/G]GGGGGAAGGCATATA	51317
rs576931479	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45974307	AAACCAAACTCCTGG[A/G]TTTAGATGACAAAAG	51317
rs576933497	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46114539	AAAGTGACGGGCTAC[C/T]ATAAAGGATTTGAAG	51317
rs576940575	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45957199	ATAAATGGAGACTTC[A/G]ATATCCCTCTTTAAG	51317
rs576944885	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46058298	GAAACATTATAGATG[C/T]TTCCTTTTTACACTA	51317
rs576964713	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46074931	ATGATATTTTTCTGT[C/T]CCATCAAGAAGGTTG	51317
rs576969239	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46072779	CCAGGTAAAGGGAGA[C/T]AGGGCAGCAAACTGT	51317
rs576988117	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46016299	TCATTTCATGACTCA[A/C]AATTTCCCAGAGTCT	51317
rs576991080	snp	A/C	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46096255	TCATCATTACTGGAT[A/C]ATTTTGTTCCTTCTA	51317
rs576997474	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46074445	TCTGCCAGAGGATAA[A/G]TGGCTCTTTTGGCGG	51317
rs577026373	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45949151	GCCTCTGTTGCCGAT[A/G]ACAGCTGTATTGAAG	51317
rs577083953	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45958203	AAGAATTAGCACCAA[G/T]CTGTCTCAAATTCCA	51317
rs577106842	snp	G/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46099747	AACATTTATTTCAGT[G/T]AAAAGGTTTTGGCAA	51317
rs577107776	snp	A/G	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46066387	CAACAGTTTTTAAAA[A/G]TTAATATGTGTTCCT	51317
rs577108807	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46107945	TGGGGATGAGGTCAG[C/T]CCACACTACTCACAT	51317
rs577132362	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46066335	ATATGTACATACATA[C/T]AAATATATATTAGAT	51317
rs577152670	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46040938	ACACACACACACGCA[C/T]GCACAATTAAGGTTC	51317
rs577170633	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46101883	TTTTTTTTTAAATAC[A/G]GAGTCTCGCTCTGTC	51317
rs577179684	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46088134	TTATAGCATCAAAAG[A/T]ATTATTGGCTACATT	51317
rs577183408	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45969711	TTTAGCTAAGCGGGA[C/T]AGACAGCTGGGCTGA	51317
rs577198454	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45982306	TCTTTTCAGACAACT[A/G]AAATATCATATAAAG	51317
rs577217878	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46067173	GGGATTTCTGTACTA[C/T]GTTGTCCTGTAAGGG	51317
rs577219482	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929222	GGCAAGCACCCCCCC[A/G]CCCCCCACCCCCAGA	51317
rs577254411	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46035270	CCTGAAAAAAATCCA[C/T]CTTTCTCTACTGATC	51317
rs577266649	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46096561	TTCTTCCTCCTCAAA[A/T]TTTTTTTTCTCTTGA	51317
rs577285619	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46027026	ATTAAAAGTCTGAGA[A/G]CAGGAACACACACGC	51317
rs577304671	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46097896	ATCCTAGATCAGGAT[A/G]ACACATAAAACTTCA	51317
rs577322372	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45970657	AATATTTTTAAAGTG[C/T]CTCAACTAACTCCAG	51317
rs577339508	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46107710	AAATTACAACAGTGA[A/G]TTATCACTAATAATC	51317
rs577377233	snp	A/G	0	0	intron-variant	PHF21A	GRCh38.p7	11:46116451	TATAGAAGAATCAGG[A/G]AACTTACATACTCAC	51317
rs577397436	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46052499	CATTCAACCTCACTG[A/C]CTATCAGTTTTCTGA	51317
rs577402961	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45934519	ACAAACCGGCAGAGC[C/T]GCCATCAGACTTCCA	51317
rs577431618	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45994761	CTCTGCAACCCAGCT[C/T]GCTTAGCTTACCCTT	51317
rs577438075	snp	C/T	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46048768	GAGCAAGACTCCATC[C/T]CAAAAAAAAAATAAT	51317
rs577440545	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931283	TAAGTTAGGTGTTGT[A/G]TGGCAACCCCCAGAT	51317
rs577450724	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45990881	GAACCTACACTGACA[C/T]CTCAATACTGTCGAA	51317
rs577458526	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46032046	AAAGCCCAACTCTTA[A/C]GTGCTGCTTTAAAAA	51317
rs577475483	snp	C/T	0.0023933	0.0345097	intron-variant	PHF21A	GRCh38.p7	11:46047973	ATATGTAATACTTTT[C/T]TAAACAGATTTATTG	51317
rs577485129	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45999458	AGTATATACTTCCAC[C/T]AGGTTCTATTCTTTA	51317
rs577496419	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46013851	ACGAAAGATGAAAAA[C/T]GGTAAACCAGCTTGC	51317
rs577498327	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46095489	GAGTAAATGAAATTA[C/T]TTTTGCTTTTAGAGG	51317
rs577531822	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978541	CAGTGAACAGCCAAC[A/T]GAACTATACTCTTTT	51317
rs577548169	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46037577	ATCCGGGAGCCGCCT[C/T]TGTTGCGGTGAGCCG	51317
rs577576142	snp	C/T	0.00199481	0.0315187	intron-variant	PHF21A	GRCh38.p7	11:46047626	TAAGAGTCTGAAAGA[C/T]ATTATTTTTTCTTTG	51317
rs577577700	in-del	-/A	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46010830	TGGACTGAGGATAAT[-/A]AATGATCAGTTCATT	51317
rs577594516	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45978003	TTAGTTTTCTCTTCT[A/G]AAAAACAGAGATGGT	51317
rs577685032	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46013768	TACTGAATACCATAG[A/G]TAACAATGGTAAGTA	51317
rs577685940	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46060907	ATGTCCTGAATGGTA[C/T]TGCTGAGGTTATCTA	51317
rs577686011	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46051595	CTTCTTGTCTACACA[A/G]GAAAAACTGAGTTCT	51317
rs577708274	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46081890	GACAGAAACCATAAA[C/T]TACCCACAAAGCCAG	51317
rs577752096	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46004590	TTCTTCAACATAAAA[A/G]TTTTAAAGAACTGTG	51317
rs577752536	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45943470	ACAGGCGTGAGCCAC[C/T]GTGCCTGCCCATCAT	51317
rs577771826	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46020775	ATGGTTGAAAAACAT[A/T]ATTCTTAAACTAAGC	51317
rs577777346	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46112589	CTCAGACTACATTTT[C/T]AAGTATTAAATTTAC	51317
rs577797100	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46034405	AATAAGGTTTCTCTT[C/T]TTTCTTTTATCCTCT	51317
rs577812607	in-del	-/CTTTATCA	0.00159617	0.0282053	intron-variant	PHF21A	GRCh38.p7	11:46083536	AGTCAATGCATCATC[-/CTTTATCA]CTTTTGAGTACCAAG	51317
rs577817132	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46044710	CAATTAGGAAATAAA[A/G]TTCCTTTTAAGGAAA	51317
rs577824357	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46036406	TTCAAAGTTTCCTTG[C/G]CTACATCTGGGTGAA	51317
rs577847383	in-del	-/A	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46094265	CAATCCTGAACTGAT[-/A]AAAGAATTTTGCCAT	51317
rs577874192	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45984288	CCAACATGCCAGGCC[C/T]CCAGAACTGCTAGTA	51317
rs577887736	in-del	-/TTC			intron-variant	PHF21A	GRCh38.p7	11:45977832	GCTTTTTTCTTTTTT[-/TTC]TTCTTCTTCTTTTTT	51317
rs577911909	snp	A/G/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46044115	TAAAATTGACTAGAA[A/G/T]CAAGTTTCAACCTAA	51317
rs577922850	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45994788	CCTTCAGATGTTCCA[A/G]TAGTAGGACGACTTT	51317
rs577928429	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45975009	GCCAAATATGAAGTA[G/T]TGATTTAAAACAGAT	51317
rs577959663	in-del	-/AAG	0.00795532	0.062565	intron-variant	PHF21A	GRCh38.p7	11:46074133	ATGCAAAAAAAAAAA[-/AAG]TTGTCAGATGCAACT	51317
rs577967605	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46068907	TCTGCCATACTCAGG[G/T]AAAATGCCCTATAAT	51317
rs577986312	snp	A/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46018723	CACATTTTTTTTTTT[A/T]AATTCAAGAAAACAG	51317
rs577995725	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46076922	ATGATGAAGCAACCC[A/G]AAGCATTTAGCCAAT	51317
rs577998258	snp	C/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45981733	AAACCATAAGAGCCA[C/G]GTTAATTCTCAAATG	51317
rs578000569	snp	A/C	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45951660	GTTCTTTTGATGAAG[A/C]AGTGTGTGGACTGAT	51317
rs578025855	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016290	ATCACCATGTCATTT[C/T]ATGACTCAAAATTTC	51317
rs578030913	snp	C/T	0.00398564	0.0444627	intron-variant	PHF21A	GRCh38.p7	11:46111654	TCAAACTAAGACATA[C/T]ACATTGCAGCTTACA	51317
rs578031288	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45970365	TTCTCTAAGGATTCC[A/T]GGATAAGCGGTGAAC	51317
rs578032617	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46011871	ACAACAAAACAAAAA[A/G]AGCAAAAACTTCTTT	51317
rs578050711	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46104556	CATTAGATAACACTT[A/T]TATCATCTATACTCT	51317
rs578055774	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45960326	GAATGAATAAACACA[C/T]TGTGGTATATACATG	51317
rs578058945	snp	C/T	0.00279162	0.0372561	intron-variant	PHF21A	GRCh38.p7	11:45950868	ACTAGGTCAGTTTCT[C/T]ACATTTATACTGCCA	51317
rs578075334	snp	C/G	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46011399	GAGGCTGAGGCAGGA[C/G]AATCGCCTGAGCCCA	51317
rs578098054	snp	C/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:45976286	ACCCTCCTTGACAAG[C/T]ACTTTCTGATCCCTC	51317
rs578145671	snp	G/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45984790	GTGCTGCAAGTCTCT[G/T]CTTTTTCACACATTC	51317
rs578152697	snp	A/T	0.000798403	0.0199641	intron-variant	PHF21A	GRCh38.p7	11:46018266	AAAAAAAAAAAAAAA[A/T]AATGTGTCCTATGCT	51317
rs578156087	snp	A/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120247	TTTTCCAAAAAAAAA[A/T]TTTTTTTAATTAAAT	51317
rs578171784	snp	G/T	0.00755907	0.0610114	intron-variant	PHF21A	GRCh38.p7	11:45949310	GTACAATCAGGGTGC[G/T]GCTCTTCAGCAGGTT	51317
rs578175940	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45944223	TGTACCTACATAAGA[C/G]AGTATCTTTGCTCTT	51317
rs578188757	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085483	TTTCTTTTCTTGAAT[A/G]TGGCCTTAGACATGA	51317
rs578189799	snp	A/G	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45976989	TTGGCAAAATCAATT[A/G]AATATGTCAGGTGGG	51317
rs578189874	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:46094435	AAGAGCTTATGGGCC[C/T]GAGATTCCTTGGCTG	51317
rs578197167	snp	A/C/G	0.00012251	0.00782569	intron-variant	PHF21A	GRCh38.p7	11:45938108	TTCCTCCTGATGGCC[A/C/G]TGTCTTTGTCCTCCT	51317
rs578213551	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45939661	GTCTCTCTACCACCC[C/G]CATCACAGTGATAGT	51317
rs578237361	snp	C/T	0.00119737	0.0244387	intron-variant	PHF21A	GRCh38.p7	11:46093267	AAACTACATGTCTTC[C/T]TTTTGCCTTAAATAT	51317
rs578251496	snp	C/T	0.000399281	0.0141238	intron-variant	PHF21A	GRCh38.p7	11:45967777	TGACTGAACTTAAAA[C/T]GACCCTGTGGTGGGT	51317
rs578255942	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086292	CCCGGCTAATTTTTT[G/T]GTATTTTTAGTAGAG	51317
rs745335430	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46024964	CCCTTCCAATAAATA[A/C]TTTCTCACAGGAAGC	51317
rs745340322	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46105050	ACTTCTACTAGTTTA[C/T]ACATTAACTCACTTA	51317
rs745350747	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45951992	TTGTATTTTTAGTAG[A/G]GACAGAGTTTCACCA	51317
rs745360757	snp	A/G	0.000185615	0.00963187	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935109	GGACAGGCCGGGCTG[A/G]GCAGTACTTACTTCC	51317
rs745376797	snp	A/C	1.65444e-05	0.00287609	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084233	ATCCTCTACCTTCTC[A/C]ACTTTCTCTGCTAAT	51317
rs745377606	snp	C/T	1.64749e-05	0.00287005	intron-variant	PHF21A	GRCh38.p7	11:45948852	ACAAAGCAAAAGCAA[C/T]AGCAGCAAGGGAGAG	51317
rs745384686	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46091547	GCTAAAAATGTACTA[A/T]CAGACATGAAGCTAA	51317
rs745415453	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46053610	CTAACCTTAATCAGT[A/G]TTTCATACAGGCTGA	51317
rs745424724	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46024302	CCTCCCTCTCTCCCT[A/C]TATCTCTTTCCTCTG	51317
rs745439893	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46002228	CATCATTATAATCTG[A/G]CACACTGGGCTAGGT	51317
rs745465926	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45947552	CTGGAAGGGGAAGAA[A/C]AAGATGAATGCTCTC	51317
rs745469384	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45948910	GGGTCCCAGGGTGCA[C/T]TGTGCTGTTTAGGTA	51317
rs745471544	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46106055	AAGGTACTGAGAACC[C/T]GACACAATGAAAACA	51317
rs745505026	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46052043	ATAGTCAATAGTCAA[A/G]GTTGAGATGATCCAG	51317
rs745505868	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46007332	TCTTTTTTTTTTTTT[-/C]CGAGATGGAGTTTCA	51317
rs745512090	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46000726	GGAGTTAGAGACCAG[A/C]CTGGCCAATAGGGTG	51317
rs745533950	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46054452	ATCCACTTACCTACT[C/T]CTACACATCTTTTTA	51317
rs745538665	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45964748	GCCTCGTTTTTTAAG[A/G]TAAAATCTGACTTCA	51317
rs745588125	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46066324	ATATTTGAGCCATAT[A/G]TACATACATATAAAT	51317
rs745624063	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46015840	CTATGGTAACAATGC[C/T]TTCGTCTGAAATACC	51317
rs745631038	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45978521	ACCAGTCCAATGTCC[A/G]TAAACAGTGAACAGC	51317
rs745657760	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45962297	AGAGAACGTTGGATA[C/T]GGGTTTGGTAACTGT	51317
rs745674353	snp	A/G	1.64784e-05	0.00287035	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971300	GAGGCAGGCATGGTC[A/G]CAGTTGCTGCTTTCA	51317
rs745724811	snp	A/G	1.64982e-05	0.00287208	intron-variant	PHF21A	GRCh38.p7	11:45936475	GCTTACAAAAAAGTG[A/G]GTATGGATAACTCCT	51317
rs745743497	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45977422	GATTACAGGCGTGTG[A/C]CACTGTGCCTAGCCT	51317
rs745755115	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45956258	ATAAAGCTAACTAGA[A/T]GAATAAATATAAAAG	51317
rs745781685	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46097219	TAAGCTTTTCAAAAT[A/C]CAAGACAGATCTTGT	51317
rs745808864	in-del	-/ATGAT			intron-variant	PHF21A	GRCh38.p7	11:46071789	TAGTTTTAAAAAATC[-/ATGAT]ATAGCCAATTATGCT	51317
rs745815546	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45993728	AACAGAGTCAGGCTG[C/T]TGAGATCCAAGGAAG	51317
rs745843157	snp	A/T	1.65307e-05	0.0028749	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971140	TGTGTTTTTTGCCAC[A/T]ATTTGGACAGCCTCT	51317
rs745867655	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46096337	TCTAGTTATTGTCCC[C/T]GTCTAGGCTCACGTT	51317
rs745881806	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46055758	TTTACCTTTAAGGCA[A/T]TTATAAGTTACATAG	51317
rs745903021	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46070778	AACCAAAAGATAATT[C/T]ATGGAATACTACAAT	51317
rs745988015	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46035005	GAAGTGGAGAACATA[C/T]GATATAAATGAAAGA	51317
rs745993847	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46019814	CAACACAGAAGCAAG[C/T]AAGAAATATTACATC	51317
rs746010263	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46107146	AAATCTCATCCTTTT[-/A]AAAAATTTCAAATTT	51317
rs746015868	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45946618	CTGACCTCATGATCC[A/G]CCCATCTTGGCCTCC	51317
rs746018428	snp	C/T	0.000159599	0.00893163	downstream-variant-500B, utr-variant-3-prime, synonymous-codon	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928906	GGGCAACCTGCCCTC[C/T]GCCATCCCTGCTATT	51317
rs746029081	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45943533	TAACTGGTCTTCCTG[C/T]TTCCATCCTATTTTC	51317
rs746051704	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45935742	TCTTCTTCTTTTGCT[-/AA]AAAAAAAAAAAAAAA	51317
rs746069068	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45941801	CTAGGCGCTGAGGAC[A/G]TATGTTTTTAGGAAG	51317
rs746075865	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46048392	TGTATGGATATACCA[A/C]ACTTTATTTAACTAT	51317
rs746094473	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46098013	CCCAAAAGATTCTAA[C/T]AGGGAGCCAGGATTA	51317
rs746103000	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46033461	GTAGAGATGGGTTTC[A/G]CCATGTTGCCTAGGC	51317
rs746103665	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997766	GTGCTGCTTGTCTCA[C/T]GGTGCAAATCAACCT	51317
rs746144377	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45941931	CACGGTACATCCAGA[G/T]GATTAGTGTCTGGTA	51317
rs746172270	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929566	CCTCTGGCCTGCCCG[C/T]CCCATCCCGCCTGAC	51317
rs746187320	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46046928	ATATTCAGAAGTCTG[A/G]GCTGTTTGTTTGCTA	51317
rs746200094	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45996910	ACTAACTTACTTTCT[C/T]TGGGCACAAATGTAT	51317
rs746203521	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46011606	TCCCACTTGGTGGTA[C/T]TAAGCACTGCTTTTC	51317
rs746206214	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45969278	GGAAGAACACTCTCA[-/G]GGAGAGTATGGTCAT	51317
rs746215204	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46080166	TTTATCTAACTACTA[-/C]GTTTTTTTTTGAGAC	51317
rs746225494	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45958616	GTCTCCAAAAAATAA[C/T]GAAAAAAATTAAATT	51317
rs746251313	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46062331	TCTCAGAACTTTTAT[G/T]AGCCAGGCATGAGAC	51317
rs746311227	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45973427	TATTTTTCTGCCTTA[A/T]GCGCATATACACATA	51317
rs746331941	snp	C/T	1.65321e-05	0.00287502	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965431	ACGTTTTGGCTATGG[C/T]TGCAGTCTGCCCATT	51317
rs746342972	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46076030	AGAGGGAGAGTGGTG[G/T]GGAAGAAACAAGAAA	51317
rs746360498	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46083051	TTTTTATCACTTGCC[A/C]TTCAGCCAAACTGGG	51317
rs746367986	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46026441	TGCATAAACAGGTGT[A/C]AAGGTTATTTTTATT	51317
rs746377849	snp	G/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932338	ATCTGAGAAGACCAC[G/T]GGTAGGGCCCTGATA	51317
rs746387842	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46115775	AATTCCTTCCCTTCT[A/C]TGTTTGAATAGTAAT	51317
rs746414312	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46034305	ATGTAAGACTAATAA[C/T]CCTTTGTCACACATG	51317
rs746415376	snp	A/C			utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46092212	CTGGCTCTCCTTCAG[A/C]TCTCTAGCCCCCTAT	51317
rs746430461	snp	G/T	1.68261e-05	0.00290048	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938159	CCACCCACAGTACCT[G/T]GTCCTGACATCTGGG	51317
rs746468813	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46027237	ACAAGTTTTCTCCGT[A/G]CTAACAGGTACAACA	51317
rs746477379	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46010890	AGTAACCAGGCAGTG[A/G]ACAGCATCATACCAG	51317
rs746494964	snp	C/T	3.62851e-05	0.00425925	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965549	CTGAGGAGCTGCGAG[C/T]ATGGGAGGTGGTGCT	51317
rs746503723	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46074459	AGTGGCTCTTTTGGC[-/G]GGAGGGGGGAAGGCA	51317
rs746512195	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46115370	TTTACAAAAGATAAC[A/T]ATTCAAAAATTTAAC	51317
rs746539829	in-del	-/TC			intron-variant	PHF21A	GRCh38.p7	11:45977842	TTTTTTTCTTCTTCT[-/TC]TTTTTTTTTTTTTGG	51317
rs746556693	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46026647	TGCAAAAAAAAAATC[C/T]TTTAAAGTCAAGCAG	51317
rs746585345	in-del	-/T			downstream-variant-500B, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929042	CCAGTTTGGGGCTGG[-/T]TTCCCCCATCTTGAA	51317
rs746592609	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45990100	CTAATTACAAAATCT[A/G]ATCCACAAATTTCTA	51317
rs746604197	snp	C/T	0.000185649	0.00963277	intron-variant, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935207	GTGTGGAAGAAAGAG[C/T]GAGGGAGGGCCGTAC	51317
rs746649405	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46092442	TGCTACTTTTCCATA[A/G]TTTTTCAAGACAAGC	51317
rs746660583	snp	A/G	1.76362e-05	0.00296948	intron-variant	PHF21A	GRCh38.p7	11:45935572	CACGTACTGTTACGT[A/G]TATTGGAAAGGCCTA	51317
rs746675231	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46082357	GCCTAGTAACCAACA[C/T]CCCTACCTTGATGTC	51317
rs746680502	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45988220	CTAGAAGAGGTAAAT[A/G]TAACAGATTATTTAA	51317
rs746680750	snp	A/G	0.000362337	0.013455	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45949426	AAAGACTGCTCCACT[A/G]TAGACCGGATTTGCT	51317
rs746705661	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46091600	AATGTAAATAAACAC[A/G]AGTCCCAAATTTCAA	51317
rs746727567	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46111657	AACTAAGACATATAC[A/G]TTGCAGCTTACACTT	51317
rs746764129	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46002427	TTTATTAACTTTCCA[A/G]TAATAACCTACCATA	51317
rs746785799	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45966057	TCCTTTGTGGGCTTA[C/G]TCTTCCTCTGCCTCA	51317
rs746790251	in-del	-/CACG/CG			intron-variant	PHF21A	GRCh38.p7	11:46114103	ACACACACACACACA[-/CACG/CG]CGCACACATCCCCAC	51317
rs746806460	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45947814	AAAATAACTTAGAGT[A/T]CTGGTTACTGTGGCC	51317
rs746812359	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46106364	AGCAATAATTACAAT[A/G]TGTTTTGCATATAGA	51317
rs746838446	in-del	-/AAA			intron-variant	PHF21A	GRCh38.p7	11:46118418	CAAAAGTCTGATGTT[-/AAA]AAAAAAAAAAAAAAA	51317
rs746842845	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929826	GGGCCAGAAGACTGC[C/T]CAGGGCTGCCCACTC	51317
rs746855865	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46052274	ACCTCTGCCAGTACA[C/G]GACAGCCTGTAAGCA	51317
rs746862003	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46071162	GGCTTCTTTTGGCTA[A/G]TGAGATGTTAACAAA	51317
rs746877812	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45964916	TGAAATCCCTTTCCC[G/T]GTTTTGTTTATTCTT	51317
rs746881137	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46038953	GCACTATCAAAGAGC[-/T]TTCCAAGCAGAGAAA	51317
rs746891776	snp	C/G	1.64887e-05	0.00287125	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971320	TGCTGCTTTCAAGAC[C/G]AGAGGTAGTGTCTTT	51317
rs746929503	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46066661	CTATGATTGTACCAC[C/T]GCACACCAGCTTGGG	51317
rs746949874	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46104674	CTGTAATAATAACAA[C/T]AATAATGATAAGAGC	51317
rs746954794	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46020594	ATAAAATACTATCCT[C/T]TTCGGTCCTATTTAG	51317
rs746958645	snp	A/G	1.64735e-05	0.00286993	intron-variant	PHF21A	GRCh38.p7	11:45948965	TGAGGGTTGAAGGAG[A/G]AAAGGTGACTGTTGA	51317
rs746979794	snp	G/T	1.64784e-05	0.00287035	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979787	CAGGTTGGGAGAGGC[G/T]GCAGCTGACTGCTGG	51317
rs746984909	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45996485	CCTTGACAGTGGCCA[A/C]ATAAATGATTTCCCT	51317
rs746994891	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45940003	ACAAGAAGCAATAAT[A/G]GAGAGGAATGTGAAT	51317
rs747004808	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46081031	CCTGCTGTGTGGTAC[A/G]CTCACTGGACTAATT	51317
rs747007817	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46042358	AACCAGAAGATCCTA[A/G]AAGCAGCCATATTAG	51317
rs747048795	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45952741	TTTGATGGCTTTATG[A/C]CACTATTTCACATGG	51317
rs747062825	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45941122	AATTTTTTTTGAGAC[C/T]GGGTCTGGCTCTGTC	51317
rs747063276	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45937043	CTAAAGTATAATCTA[A/G]ACCCTATGTCAAAAA	51317
rs747077675	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46058072	CAACTTTTAACAAAG[C/T]CTTGTTAAATGTGAA	51317
rs747104694	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46072378	AGGGCTTGCTCTTTG[C/T]TGCTTCTCCCCCTTC	51317
rs747106223	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46023526	GTGTCATATGGAATA[C/T]TGGTATCCCCTCAGA	51317
rs747133270	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46006008	GCACAATTTTAAACT[C/T]TGAAAATGGGCTGGT	51317
rs747168429	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45968397	ACCTCAACTCTAACT[A/C]ACTCTAGCCTGCATG	51317
rs747169788	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46013859	TGAAAAACGGTAAAC[A/C]AGCTTGCAGGACTGG	51317
rs747183580	snp	A/C/T			intron-variant	PHF21A	GRCh38.p7	11:46094362	ATAGAAAATCAAACC[A/C/T]GGAAAAGTTAAGTGA	51317
rs747186526	snp	A/C	1.65127e-05	0.00287334	intron-variant	PHF21A	GRCh38.p7	11:46076733	ACGTTAAAAATATGC[A/C]CCCCTCCCCTTTTCC	51317
rs747188891	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46036078	CTAAAGTAGTGCTTA[C/T]GGAAAGAAGATAGAT	51317
rs747189325	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46109317	CTAAATAAGATCCTA[C/T]GTGTAAAAAGGCTTA	51317
rs747248838	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46021651	GGCTCAAGCGATCCT[C/G]CTGCCTCAGCCTCTC	51317
rs747258401	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45983880	GGTTCTCACTGCTCC[C/G]TATATAAAGGATATC	51317
rs747272820	snp	C/G	1.65329e-05	0.0028751	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953554	CTCCCGTTTTGGTTT[C/G]GGTGCAGCAGGTGGG	51317
rs747279054	in-del	-/CG			intron-variant	PHF21A	GRCh38.p7	11:46040931	ACACACACACACACA[-/CG]CACGCACGCACAATT	51317
rs747288742	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46069703	ATCTGGATTCTAGTA[C/T]TGAATCTCATACTGA	51317
rs747292441	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46087185	ATATGCACATCTTTT[C/T]AAACAAGAAGACATT	51317
rs747337419	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46115043	AAGGCAGAAAACATT[C/T]CTGTAACTGATTCCA	51317
rs747338557	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46035132	CCTCCCAATATGTCC[C/G]CTCTCTTTTTGGCTT	51317
rs747382214	snp	C/T			synonymous-codon, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934151	GATGAGGCGAATCAG[C/T]TGTTTTACCTTCTCC	51317
rs747392354	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45998002	GATGGCAGCACAGTT[C/T]TGCTCCTATCAAAAC	51317
rs747461992	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45942258	AGAAGCTCTTAGTTT[G/T]TGAGTTGATGAGTGG	51317
rs747487755	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46063182	ATGAATTGAATTCGC[C/G]GGGGGGGCTGGCATG	51317
rs747498734	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45974940	GGCAAATACTGCCAA[C/T]AGCAAAATCCTTTTT	51317
rs747531028	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46077271	TCTCCCTTATTTAGC[A/G]AAGTACATTTGTTAT	51317
rs747548124	snp	C/T	1.65463e-05	0.00287626	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945934	TCAGGGGAGTCAGGA[C/T]GACTGGATTGGGGGG	51317
rs747555644	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46064853	GATTTACCCTTCTAA[C/T]AATGTATTGCTTTGG	51317
rs747596415	snp	C/G	1.65427e-05	0.00287595	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945944	CAGGATGACTGGATT[C/G]GGGGGATGTTGGGGT	51317
rs747624336	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46049071	CTGACAACAGGGATG[A/T]CAATGCTTCACACCA	51317
rs747643238	snp	C/T			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46118026	CAAAAATTTCCTTTA[C/T]CTTGCTGTAGCACCT	51317
rs747651885	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46082096	CATCACAGGACATTA[C/T]TATTTAAATATTTAC	51317
rs747679553	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45960499	ACAGGTACATCTATG[C/G]AGACAGAAAGCAGAC	51317
rs747705161	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46012108	TGTTCATTACTACCG[A/G]AAAGAATCCTTCAAC	51317
rs747712458	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45963421	GTAAAACTCTGTGTC[-/AA]AAAAAAAAAAAAAAA	51317
rs747759245	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46116539	GGACATACAATTCAC[A/G]GGATCTTCAAAAGGG	51317
rs747767765	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46076032	AGGGAGAGTGGTGGG[A/G]AAGAAACAAGAAAAC	51317
rs747784708	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46077479	AATTCCAAAATTAAA[A/G]TTTTCAAATGCTTAA	51317
rs747832010	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46042223	CTGTGGGAAAGCCAC[A/G]TGACAAAACATATTC	51317
rs747837928	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45994762	TCTGCAACCCAGCTC[A/G]CTTAGCTTACCCTTC	51317
rs747848679	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45974565	TCAAGTAATCCTCCC[-/A]ATCTCATTCTCCTGA	51317
rs747867959	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005325	TAAAATTTATACAAA[C/T]TTATGCTTGGGACCA	51317
rs747878768	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46076304	ATTAACATAAAGGCA[A/T]GACCATACTTAGAAT	51317
rs747897147	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931397	CAACTAGTCCAGGCA[C/T]CTCCAAGGCTCCCTG	51317
rs747910695	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46108980	CCATCCCATTCCAAT[A/G]TTTACTATTTTCAAA	51317
rs747925695	snp	C/T	0.000182963	0.00956284	intron-variant	PHF21A	GRCh38.p7	11:45935598	GCCTAGGTCTCTGCA[C/T]CTATGTATCGACTGC	51317
rs747948585	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45950481	GAAGAAGAATTGTCT[C/T]GAGCCACACATAAAA	51317
rs747967917	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46055457	CCACCAGAACTGGCA[C/T]TCAGAATGAGGAGTG	51317
rs747971329	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093116	TGTTTCTATGCCACA[C/T]ATCTAATCAGTGATG	51317
rs747976600	snp	C/T	1.64776e-05	0.00287028	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979944	ACTATCAGGTTCTTC[C/T]GTAGCTGTTCAACTA	51317
rs747997908	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46101481	GGGAATAGGTACGTG[A/G]GGTTATATTATTCAC	51317
rs748015069	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46017791	CCCCTAGAAATAAAC[A/C]AAGGTTCCACAGAAA	51317
rs748023209	in-del	-/AA	0.000117331	0.00765843	intron-variant	PHF21A	GRCh38.p7	11:46076848	AAAAATATCTGTGAG[-/AA]AGATATTTCATTTGT	51317
rs748036764	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45966966	ACCCTGTGGGCAAAA[C/T]GCTTTCCCCTTATGC	51317
rs748036823	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45949645	CTACTGGAAGCAAAT[A/G]TGTAGGACCATCTAC	51317
rs748037044	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46004406	AGGAAATGGATTTCA[C/T]TTTTAATAGATAAGA	51317
rs748037205	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45983136	GCTAGAGCAAGGTGA[C/T]GACCAATCAGAACCA	51317
rs748038572	snp	C/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45949448	GGATTTGCTGTTGTT[C/G]TTCTTTTTCGCTCTT	51317
rs748053968	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46054281	TGAAAATTATATCAC[A/T]TAAAGTTTCTTCTCT	51317
rs748084478	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45938731	GAATGAGGTCTATCT[A/T]CTTTTTTCTTTCTCA	51317
rs748123143	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46019765	CTTGACAGTTAAACA[A/G]TAGCTCTGCTCTAAA	51317
rs748150404	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45994992	CCACAGAAATGTGTA[C/T]AATCTCTGTGCTATA	51317
rs748201292	snp	G/T	1.70504e-05	0.00291975	intron-variant	PHF21A	GRCh38.p7	11:45938136	CCTCGGCCCCTCCCC[G/T]GTTGGACCCACCCAC	51317
rs748229248	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975937	AATATATGCCATATA[C/T]AACCTCCCATTCGTC	51317
rs748229702	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46097463	CTTTTCCTCCAAATA[C/T]CTTCATGGCTCACTC	51317
rs748256179	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45939773	GGAGAACATAGCCCA[-/AA]AAAAAAAAAAAAAAA	51317
rs748263265	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46060902	TGCTTATGTCCTGAA[C/T]GGTATTGCTGAGGTT	51317
rs748267423	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46043652	AAAAAAACTGACCCA[C/T]TTTTAGAAGTCAGCA	51317
rs748269103	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46113244	GCAAGTTTCAAGAAA[A/G]TCTGAACTATCTAGC	51317
rs748296198	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46009567	ACGCTATGTATTACA[C/T]AATTTAATCTTCAAA	51317
rs748307571	snp	A/G	2.08535e-05	0.00322898	intron-variant	PHF21A	GRCh38.p7	11:45965295	CTACTGCCCAGAGCA[A/G]GTACATACTCTGCCT	51317
rs748311500	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45954439	CAGAACCACCCTTAC[A/G]TGGAATATTAAAAAT	51317
rs748319823	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46096436	CACAACCCATTAGGG[C/T]CTTTGCCTCCCTCCA	51317
rs748320509	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46073327	GCGAGACCCCGTCTC[-/A]AAAAAAAAAAAAAAA	51317
rs748321099	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45993782	GAAAGGGCCAAGCAG[C/G]AGAGGAGCCAGTGGA	51317
rs748376763	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119559	CCCTCATCACAACAA[C/T]TCAACTACTTAGAAA	51317
rs748397500	snp	A/G	3.29554e-05	0.00405914	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45936510	TGCTTTGTAGGCAAT[A/G]TAGGAATGAACAATT	51317
rs748404837	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46007221	CTAAGAGATGAGAAA[A/C]GGGCCCCCTGTCTTT	51317
rs748416195	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45935401	GAAAATCCTCTCTCT[A/G]ATTAAAGCCAAGAGG	51317
rs748429647	snp	C/T	1.67142e-05	0.00289081	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965375	AGCGAGTCTGGTCCC[C/T]GGAGTAGCTATCACA	51317
rs748433395	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45950173	AAGCTGTGGGCCAGA[A/G]AAAAAGGCAGTGCCA	51317
rs748436911	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45968787	ATACAAAAATTAGCC[A/G]GGCGTGGTGGCACAT	51317
rs748451265	in-del	-/AG			intron-variant	PHF21A	GRCh38.p7	11:46083246	CTCTGCAGCGGAACA[-/AG]AGTTTAACGAGATCC	51317
rs748453075	snp	A/G	1.72591e-05	0.00293756	intron-variant	PHF21A	GRCh38.p7	11:46079111	AAATTTAACAATTAA[A/G]TGAATAACAATAGTA	51317
rs748458906	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46023731	GAGACAGAGGTGGGC[A/G]GATCGCCTGAGGTCA	51317
rs748464505	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46072508	GGAACCACTCTCAGC[A/G]GCCCTAGCCCTAGGG	51317
rs748524691	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45984442	ACAGAGCCTCTGACA[C/T]TTCAAGTCACAGTTT	51317
rs748551196	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45945387	GCAGAGTTTCTGCTC[A/G]ACAGTTTCTGATCAA	51317
rs748598423	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46062166	TCACCACGTTGTGCC[C/T]TGGTATGAGGGTGTG	51317
rs748605793	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46104423	AAAAAAGAAAAGCTT[A/G]TATCACTATGGGTTT	51317
rs748610955	snp	A/G	1.68462e-05	0.00290221	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934032	GAGGGGGAAGGGGCC[A/G]GCGTGGAGGTGGCGG	51317
rs748638963	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45961786	CCATTTTAGAGCGCT[A/G]GAGAGGACAAGGACA	51317
rs748690004	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46051579	CTTCAGAAACACAAA[C/G]CTTCTTGTCTACACA	51317
rs748695596	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46102298	AACTCAACATGTAAC[C/T]ATAATTAATTTCCAA	51317
rs748703396	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46058521	TATTTGCCAAATGAA[C/T]TGAGGTTTAAAACTT	51317
rs748712860	in-del	-/A/AA			intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119750	GGTCAGGGGAAAAAA[-/A/AA]AAAAAAAAGAAATCC	51317
rs748724067	snp	A/C/G	6.64125e-05	0.00576216	missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934071	GGGGGGGTGCAGTCC[A/C/G]GGCCATTGGAGATGG	51317
rs748727966	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45943969	AACTGGCTATCTTTT[C/T]AAAAACGTCAATGTT	51317
rs748739458	snp	A/G	0.000132411	0.00813559	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934094	GGAGATGGCCCCCAC[A/G]GTGGCCTCAGAGTCT	51317
rs748775163	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46036610	AAGTAAAGGTACAGG[C/T]ATACATTTCTTGTGA	51317
rs748801722	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46000309	CTCTCACCTCTAGCT[C/G]TAACAGAAGCTAAGC	51317
rs748812383	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46104566	CACTTTTATCATCTA[C/T]ACTCTTTCTCACCAC	51317
rs748829548	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46066097	ATAGTCTCATAAACA[C/T]GTTGAACAAAATAAG	51317
rs748862496	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45999208	ACAGAGAAGAGAGCA[A/G]TAAATAGAGAAAACA	51317
rs748875715	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45962162	AGTTTATCCACCTTA[C/T]ATATAGACATCACAT	51317
rs748887148	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45990514	ATCCACCCGCCTCAG[A/C]CTCCCAAAGTGCTGG	51317
rs748887452	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46015510	CAATAATAAATTAAC[C/T]TTAGCTTAGTGTAAT	51317
rs748890877	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46028650	ATGATCTCGGCTCAC[G/T]GCAACCTCCGCCTCC	51317
rs748891753	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45956771	TGAAGAACAAAAAAC[A/G]TAAGATATACAGAAA	51317
rs748900403	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46102518	TCAAAATATTTTAGC[A/C]ATTCACAACACCAAA	51317
rs748917561	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46065086	CAGACATTGTTAACT[G/T]TCTTGAATATCCATT	51317
rs748967157	in-del	-/AAAAC			intron-variant	PHF21A	GRCh38.p7	11:45975377	AAAATAAAATAAAAT[-/AAAAC]AAAACAAAACAAAAT	51317
rs748978929	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46025035	TCTTAATCTTGTCAT[G/T]AACACTATTAGCCAG	51317
rs748979964	snp	A/C	1.64741e-05	0.00286998	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971270	ATAGCAATGGTAGGT[A/C]TCTGGCCCACCACAG	51317
rs748984095	snp	C/T	1.65559e-05	0.00287709	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946069	GGGGGAAAATGATCT[C/T]ACATACCTTTGGCCA	51317
rs749043938	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46096043	CTTCCTAACTTCCAA[C/T]AGAAAGCAAGTAAGT	51317
rs749086519	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45975527	TGTATACTCAAACAA[A/C]CACAAATAGAAACTT	51317
rs749119706	in-del	-/AAAC			intron-variant	PHF21A	GRCh38.p7	11:45962434	TGAAATATAAATAGA[-/AAAC]AAGGATAGTTGAAAG	51317
rs749123863	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46042289	TGAACCAAACTTTAA[A/G]ATTGCTGGACAGGTA	51317
rs749172917	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45972436	CACCTTTACTGTATA[-/T]TTGCACTGTCTGATT	51317
rs749173927	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45992022	TACAAGAGAATGAAG[C/G]AGGCCAGGTGTAAGA	51317
rs749181999	snp	A/G	3.30267e-05	0.00406353	intron-variant	PHF21A	GRCh38.p7	11:45935612	ACCTATGTATCGACT[A/G]CTGAAGGCATGAGGT	51317
rs749202903	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46094535	ACAATAAACACTAGC[A/G]AAATATTTTTGGAAA	51317
rs749211943	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46041317	GTCATTAACAAATGA[A/G]ATCTTATTTAGGATG	51317
rs749219364	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45950920	TGATTTTCAGGAATG[A/T]CAGCAGGTGTTTCTG	51317
rs749242467	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46040705	TTACATGAAACTGCA[C/T]ACTATGTTGGAGAGC	51317
rs749244012	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46095826	CTACTACAAATTTCA[A/G]ATGATTAAGTTTATA	51317
rs749282539	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45968302	ATGCTTTAATGAATG[A/C]CTGCTGCTCCTAGGA	51317
rs749290647	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46109057	TGATACACTGTAGCT[A/G]TGGCCATTTCAGTAA	51317
rs749327931	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45941866	GCTAAACAATTTTTA[A/T]AATTATGTTAACGTA	51317
rs749330386	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118850	GAAGGAGGGGGCCAG[C/T]CTTCAAAGACCAAAA	51317
rs749332340	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45966788	GCACGCCCAGCTAAT[A/T]TTGTATTTTTAGTAC	51317
rs749332432	snp	C/G/T	5.95544e-05	0.00545658	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928902	ACCAGGGCAACCTGC[C/G/T]CTCCGCCATCCCTGC	51317
rs749360727	in-del	-/AATT	1.66563e-05	0.0028858	intron-variant	PHF21A	GRCh38.p7	11:45935780	GGAACGGTTTTTGAC[-/AATT]AATTCTTTGAAATGT	51317
rs749381550	snp	C/T			missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979804	CAGCTGACTGCTGGG[C/T]GTGGTGGTGGTGGTA	51317
rs749392471	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45996676	AAAATGAAAGGCAAT[G/T]TTGAAAGTAGGTGTT	51317
rs749413512	in-del	-/A	1.65225e-05	0.00287419	intron-variant	PHF21A	GRCh38.p7	11:45979981	CTACCAAATGAAGAC[-/A]AAAAAGAAATAAAAG	51317
rs749416748	snp	C/T	1.69548e-05	0.00291154	intron-variant	PHF21A	GRCh38.p7	11:45938148	CCCTGTTGGACCCAC[C/T]CACAGTACCTGGTCC	51317
rs749417452	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46032223	TATATTTTCCTATTT[A/G]TAAATGTAATATAAT	51317
rs749421186	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46046818	TCTGGACAAACGAGA[A/G]TAGTTTCCAAACACT	51317
rs749428496	in-del	-/TG			intron-variant	PHF21A	GRCh38.p7	11:46021547	GCATGTGTGTGTGCA[-/TG]TGTGTGTGTGTTCAG	51317
rs749441061	in-del	-/TCTCTC			intron-variant	PHF21A	GRCh38.p7	11:46038115	TTGTATACTCCTATT[-/TCTCTC]TCTCTCTCTTTTTTT	51317
rs749473603	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45940397	AACAGGGTTTCACCA[C/T]GTTGGTCAGGCTGGT	51317
rs749493203	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46116280	AAAATGATATATCCA[A/T]ATATACCTAATACTA	51317
rs749507233	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46045758	TTTTGGAAGCCCTAC[C/T]CTTGCCTTCTGTGAG	51317
rs749509550	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46101860	GTGCTGGTCTCCCTC[-/T]TTTTTTTTTTTTTTT	51317
rs749528283	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46010543	GGAATAGTGGTATGA[A/G]TAACTCAAAATTAAA	51317
rs749530437	snp	A/G	1.89636e-05	0.0030792	downstream-variant-500B, utr-variant-3-prime, synonymous-codon	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928852	CGAGGCTGAGGCTGG[A/G]CCGGCGCTGCCCCTC	51317
rs749535040	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45995412	AGGAATCATTCTTAC[A/G]CAGGGGTGCATACCT	51317
rs749559151	snp	A/T	1.65334e-05	0.00287514	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938294	TGCAAACGCTGCAAA[A/T]ATCCTCATGAATATC	51317
rs749564346	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46114821	ATCAATTCCTTTCTG[A/C]TGCTCCTTCTCCTCA	51317
rs749601866	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45935371	TGTAGCTGTTACTTA[C/T]TCAGCCTGAAGACTG	51317
rs749613839	snp	A/G	1.65611e-05	0.00287755	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965405	AATGCTGGTGAGCTG[A/G]GCCATGGGGAACGTT	51317
rs749648099	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46059577	ACTACACACATGCCA[C/G]CACACCTGGCTAACT	51317
rs749653062	snp	A/C			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933410	GATACACTGTCCCAC[A/C]CCCTGCTCCCTCCAG	51317
rs749655482	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45971789	TCATTTCTATCCTAA[C/G]TGCTACAAGCTCACC	51317
rs749662029	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46058241	ATAACCTCACAACTT[C/T]CAATCATTTACTTAG	51317
rs749690660	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45970341	TATCTGGTTGAGTGA[A/C]CTCGTTGCTTCTCTA	51317
rs749705930	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46024891	TCCCTTTTCTATACC[A/G]TAGTGACTCCTAGTT	51317
rs749714836	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46022650	ATTTTTTTTTAGAGA[C/T]AAGGTCTCACTATGT	51317
rs749728327	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45955263	ATCTAAGCGAGAATC[A/T]CTCAAGTCTTTCTCT	51317
rs749740019	snp	A/G	1.6525e-05	0.00287441	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934192	GCATCTCCTTCTGCC[A/G]GGCCAGGATGGTGTT	51317
rs749756234	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46038148	TTTTTTTAAATGGAG[G/T]TTTGCTTTTTTTTTG	51317
rs749761719	snp	A/G	1.66893e-05	0.00288867	intron-variant	PHF21A	GRCh38.p7	11:46079121	ATTAAATGAATAACA[A/G]TAGTAGTTTTACCTG	51317
rs749765003	in-del	-/TCCAAAT			intron-variant	PHF21A	GRCh38.p7	11:46081633	CAACTTACTGGACCA[-/TCCAAAT]CCCTAGTAACTTTAA	51317
rs749817941	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46086361	CCTGACCTCGTGATC[C/T]GCCCGTCCTGGCCTC	51317
rs749818416	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46030811	TAAACCACATAGTGT[-/G]TGTGTGTGCGTGTGT	51317
rs749831036	in-del	-/TTT			intron-variant	PHF21A	GRCh38.p7	11:45986403	ACTGCCTTTAATTTG[-/TTT]TGTCAAACAAGAAAG	51317
rs749833352	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45985402	CTAAGTGAAGATTTC[A/T]CCATTTTATGAACAA	51317
rs749838069	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45947120	CTCCTAACTGAGAGA[A/C]CTGATTTGTGTAAGA	51317
rs749838628	snp	C/T	1.80445e-05	0.00300365	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965321	TGCCTGTACCTGTTT[C/T]TCAAGACTTGGCTTG	51317
rs749861689	snp	A/C	8.25757e-05	0.00642503	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084220	AGTCTGCAACTCCAT[A/C]CTCTACCTTCTCCAC	51317
rs749898373	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45966676	CCAGGCTGGAGTGCA[A/G]TGGCGCGACCTCGGC	51317
rs749913573	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46027572	AGTCTTTAATGCACA[C/T]AACTCTTTCAAGAAT	51317
rs749923960	snp	G/T	1.6473e-05	0.00286988	intron-variant	PHF21A	GRCh38.p7	11:45950165	CAGGAACAAAGCTGT[G/T]GGCCAGAAAAAAAGG	51317
rs749967548	snp	C/T	1.66103e-05	0.00288182	intron-variant	PHF21A	GRCh38.p7	11:45950299	ATGCTTCAGTCTGGG[C/T]TCTCACAAAGCCAAT	51317
rs749975522	snp	C/T			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935060	GGGAGAAGCCTCTGT[C/T]CCCCTGCTGCAAATA	51317
rs749988281	snp	A/G	1.6476e-05	0.00287014	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979766	CACATTTACCTGTGA[A/G]GCAGTCAGGTTGGGA	51317
rs749990087	in-del	-/CTT			intron-variant	PHF21A	GRCh38.p7	11:46100919	AGTCAAAAGTCCCTC[-/CTT]GACAAACCATTTTAT	51317
rs749991850	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46019034	AATAAGGCAAGAAAA[A/C]GAAAGGGGGAAGAAA	51317
rs750008821	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46060073	TATAAATTTATGGAA[C/T]AGAAAAAAAGACTTA	51317
rs750025387	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46057315	TTTCCCATCAGCCTT[A/C]CTCAGCCAGGATTCC	51317
rs750037206	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46083806	TAAAAACTTTAGTAC[A/G]TATGGTAGTTGAGTT	51317
rs750041794	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45980927	TAGGGATTTAACTGC[A/G]TGGAGTGAAAAATTA	51317
rs750054339	in-del	-/G	0.000185684	0.00963366	intron-variant, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935172	CTGGTCAGGAAAACC[-/G]GGGAAATGCAATCAG	51317
rs750063787	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45936092	AGACCAGCCTGGGTG[A/T]CATGGCGAAACCTGT	51317
rs750077851	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46033086	TGTTTTATTAGTTTT[G/T]ATGTATCCTGTGACT	51317
rs750081261	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46068043	GTGTAGAGAAGAGGA[C/T]GTGTGAAGAAGGCAC	51317
rs750125683	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46089004	TCAAAACTTGACTCA[C/T]CAACCAACATTTCTT	51317
rs750135704	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45997484	TGCCAAAAGATGAAG[C/G]CAGCCCATGCCTACG	51317
rs750146481	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45941617	AAATGAATATAAAAT[C/G]CCAAAACATTTTACC	51317
rs750151158	snp	C/T	1.64773e-05	0.00287026	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938245	TGATATACACGGGAA[C/T]ATGTGTCGCACATCA	51317
rs750159691	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46099330	AAACTCCTGCTGCAT[C/T]GATAGCCAAGAATAA	51317
rs750169255	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45962618	GAACATTGGCCAGGC[A/G]TGGTGGCTCATGCCT	51317
rs750171235	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46082120	TATTTACTGAACATC[A/T]ACTATGTGTACATTG	51317
rs750181359	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46046431	CAAACCAAACCCAAA[A/C]CAAAAAACCTTGCCA	51317
rs750189790	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45939509	AAAAAGCCAAAGCAA[A/C]AGCTGACAATGTTCT	51317
rs750223230	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45957860	GAATCTTCGAAAAGA[A/G]TAACAAAATCGACAA	51317
rs750223852	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45996338	AGTGATCTATATTAC[A/C]ATTAGATCACATTGG	51317
rs750249302	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46010047	GAAGTCTGAGGAACA[C/T]TCATTTAGTTGCTTA	51317
rs750249619	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46098244	AAAATCCACAATTCA[C/T]AGATGGGTGTAGTAA	51317
rs750255245	snp	A/G	4.24007e-05	0.00460419	downstream-variant-500B, utr-variant-3-prime, synonymous-codon	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928876	GCCCCTCATCTTAGC[A/G]TTGGGCAGACACCAG	51317
rs750270114	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46113687	AAAAATTAGTTGGGC[A/G]TGGTGGCGCACGCCT	51317
rs750283703	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46061925	TGTCTCTATTCTATC[C/T]CCGGACTTGATCAAG	51317
rs750327073	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46060704	TTTAAGTTCCATATA[A/G]ATGCTGGATATTAGA	51317
rs750336174	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46030289	GACAATATAAAATTA[-/T]TTTTTTCTCTCCATA	51317
rs750337585	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46114473	GGCACACAAATTTAA[C/T]GCAATCCAGCTAAAA	51317
rs750397114	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45971064	TATACTATACAAATG[C/G]GTATCCTAACCTTCT	51317
rs750397205	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46008531	GTCAAAGGTAGAAGA[C/T]GGGAAAAGAGTCTGC	51317
rs750416828	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46050882	CTCTACTATTTGCCA[G/T]AGAGGCAGCTGCTGG	51317
rs750425450	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46113014	CTTTAGAATTTGAGC[A/G]GCATAATAATCATAA	51317
rs750447716	snp	C/G	3.32325e-05	0.00407617	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934061	GGCATTGGCAGGGGG[C/G]GTGCAGTCCGGGCCA	51317
rs750449728	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45988577	GTAATAGCACAGGCA[C/T]ATAAATTTTAAAAGA	51317
rs750468836	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46088508	TAAAAAGGTCAGCCA[C/T]GGTATCTGGAAAGCA	51317
rs750521494	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45944901	CCTCCAGAGTAACTG[C/G]GATTACAGGAGCACG	51317
rs750528766	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45969014	GGTATTTACTAGGGA[-/T]TTTATCTGATAAACA	51317
rs750558903	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46103331	TAATACTATATATTT[A/G]CTATGCTAATTTTAA	51317
rs750581369	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46103808	TGATCAGTAGTGAAT[A/G]AACAAAGTTAATTAT	51317
rs750584861	snp	C/G	1.64857e-05	0.00287099	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934141	CGATGCCGTGGATGA[C/G]GCGAATCAGCTGTTT	51317
rs750588120	in-del	-/AGCAT			intron-variant	PHF21A	GRCh38.p7	11:46027082	TATCTGATGTGTGAG[-/AGCAT]AGCACACAGCACAGC	51317
rs750604074	snp	A/G	2.62347e-05	0.00362169	intron-variant	PHF21A	GRCh38.p7	11:45969932	GAAGATAAATAAACC[A/G]GAGAGAACAATTACT	51317
rs750610677	in-del	-/TGT	1.64852e-05	0.00287094	cds-indel, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979827	TGGTGGTACTGCTGC[-/TGT]TGTTGTAGTTGCTGT	51317
rs750626470	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45961299	GTCTGCATGAAAAAT[C/G]AAAGGTAGGCAGGTG	51317
rs750633870	in-del	-/CC			intron-variant	PHF21A	GRCh38.p7	11:45983203	TTCACAACTGCTCCT[-/CC]CCCCCAGGGCCTGAA	51317
rs750649013	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46102014	AGGCATGTGCCACCA[C/T]GCCCAGCTAATTTTT	51317
rs750681100	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46117577	AAAAAACTACAAGAA[A/G]TCTAAAATTTTTTCA	51317
rs750714275	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45960216	CAAGTAGTCATACAA[A/G]TGCTTGCACATGAAT	51317
rs750716760	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46063121	GAGAGGAATAGAGAC[A/G]AAGAGAATAAAAAAT	51317
rs750718116	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45976112	CGTTTCGTGGATCAC[A/G]CACTCCAACCACACC	51317
rs750773115	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46094825	GAATCACTTGAACCC[A/G]GGAGGCAGAGACTGC	51317
rs750789604	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:46116329	CTTTTTCACTGTGAA[-/AC]AAGCTTGAAAGCTTT	51317
rs750804686	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46077139	AAAGTATCCATTGAC[A/C]GAAAACCCAAAGCTC	51317
rs750806152	snp	C/T	2.70544e-05	0.00367784	intron-variant	PHF21A	GRCh38.p7	11:45965649	TTGTATTACTTAAGC[C/T]GCTCAAGTCCTATAA	51317
rs750836478	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46037339	TAGCCTTCAGGCCTA[C/T]TGATAAAAAATGGAG	51317
rs750842073	snp	A/G			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123032	GGGGTGGGGGGTTTT[A/G]TTTTTAAAGCTCAGC	51317
rs750846220	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46027185	CTGCTTTTTCTCCCT[A/G]ATTTTATTATATTTC	51317
rs750849608	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46005732	AGCAATGAATAAAAG[A/T]ATAATATTTGTAGCA	51317
rs750863694	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46041872	TAAATACACTAGTAG[C/T]CATTTCTATTACAAA	51317
rs750875268	in-del	-/TC			intron-variant	PHF21A	GRCh38.p7	11:46034332	CATGTGTTAAAAATA[-/TC]TGTCTTGAATTTTTT	51317
rs750909576	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093528	GTTCTCAGGCCCATG[C/T]AAATAACAATTTTAA	51317
rs750922454	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46069726	CATACTGATAAATTA[C/T]ACAATAATGGTTAAG	51317
rs750941342	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45950125	TCCAATTTTCTATTC[C/T]AGGAATTCAATCAAA	51317
rs750960518	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005042	TTTAACACATGCATG[C/T]ATACACCCAACTAAT	51317
rs750979227	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45936102	GGGTGACATGGCGAA[A/G]CCTGTCTCCACCAAA	51317
rs750994805	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46108387	ACAATCAATCTAAGG[C/T]ATTAGGTTTGGAATC	51317
rs751033054	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45951616	CCTTAGAAATATAAT[C/G]AAGATCAAGAGGCTT	51317
rs751035195	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45968790	CAAAAATTAGCCGGG[C/T]GTGGTGGCACATGCA	51317
rs751040961	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46058344	CATTGTTGGTAAAAC[G/T]AAACCTGATTAAGAC	51317
rs751041548	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46118420	AAAGTCTGATGTTAA[-/A]AAAAAAAAAAAAAAA	51317
rs751044098	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45991721	TCAGTTATTTACCCA[A/G]TCTTGGTCTCAGCTT	51317
rs751045065	snp	C/T	4.95054e-05	0.00497496	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935703	TGTTTTAAATCTGAA[C/T]TCCATTTAAGTAACT	51317
rs751058019	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931832	ACAAATCTGACACAA[C/T]TTACTTCTGACAAGG	51317
rs751065490	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45973078	GTGAGACTTCGTCTC[-/A]AAAAAAAAATAAATA	51317
rs751080422	snp	G/T	1.66178e-05	0.00288247	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953595	GGCTCTCTGTTTGTT[G/T]CTCATCTGTTTCTGT	51317
rs751081973	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46057213	CTTGTTTATTTTCCA[C/T]CTTGGAACTACATAA	51317
rs751084334	snp	A/G	6.75394e-05	0.00581078	intron-variant	PHF21A	GRCh38.p7	11:45935766	AAAAAAAAAAAAAAG[A/G]AACGGTTTTTGACAA	51317
rs751098755	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46022621	CACATGCCACCATGC[C/T]AGTGTAGTTTAATAT	51317
rs751102550	snp	A/G	1.65192e-05	0.00287391	intron-variant	PHF21A	GRCh38.p7	11:45950192	AAGGCAGTGCCAAGA[A/G]TATCTTCTCTTACCT	51317
rs751116160	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45937626	GCTGGGATTACAGGC[A/G]CCTGCCACCATGCCC	51317
rs751119670	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46110425	TGTCAAAGGTCTCTA[C/T]ACTGAATCTACATGG	51317
rs751132403	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46005197	TCCAAAACTTTTTGA[A/G]CACTGACGTGATGCC	51317
rs751160306	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46087979	CTAGGCTGGTCTTGA[A/G]CTCCTGGGCTAAAGT	51317
rs751189182	snp	A/C	3.31257e-05	0.00406962	intron-variant	PHF21A	GRCh38.p7	11:46076706	CTCGAGCAGACATAT[A/C]TTTAGAACACAACGT	51317
rs751203422	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45967966	TCTGGTTACAATCCA[A/C]TAAACTGCTTTCACA	51317
rs751234982	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46020752	TGTCCTATAAAGCCA[C/T]GATAGTTATGGTTGA	51317
rs751250282	snp	C/G			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122380	CCTCGCCACCCCGCC[C/G]CCTTTCCAAATAACT	51317
rs751260183	in-del	-/CAC			intron-variant	PHF21A	GRCh38.p7	11:46040926	ACACACACACACACA[-/CAC]ACACACGCACGCACA	51317
rs751276855	snp	C/T	3.49247e-05	0.00417865	intron-variant	PHF21A	GRCh38.p7	11:45953487	TGAGAATAAACCATA[C/T]ACCATAGACTGAGAC	51317
rs751326991	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46034642	TCCAGCTCATGACAG[C/G]TCTCCCAGTGGCTAT	51317
rs751330355	snp	G/T	1.80442e-05	0.00300363	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933962	GCTTCTCCTAGAGGG[G/T]CTCTGTTATTTAGTC	51317
rs751353654	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45998212	TGTTATTAGCACACA[A/G]ATTTAAAGCAGTTTA	51317
rs751359959	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46033272	TTGTTGTTAGTATTA[C/T]TGTTGTTGTTGAGGC	51317
rs751365166	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45943068	TATGCAGACGTGATC[A/T]CTTTTCTCCATCTCT	51317
rs751369872	in-del	-/ATT			intron-variant	PHF21A	GRCh38.p7	11:45974424	AAACGACAAATTATT[-/ATT]ATTATTATTATTATT	51317
rs751383046	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45981081	GGTTCACAACTATAC[A/T]CTGCACTTATAACTA	51317
rs751390892	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46059465	CAGGGTTCCACTGTC[A/G]CCCAGATGGGAGTGC	51317
rs751448466	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46048010	AATTCATATATCACA[C/T]AATTCATCCATCTGA	51317
rs751449650	snp	A/G	2.27803e-05	0.00337486	intron-variant	PHF21A	GRCh38.p7	11:45965625	TATAGGGGAAAGAGA[A/G]AATAATTATTGTATT	51317
rs751455267	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45959806	CATGTAACTGGTAAG[A/G]GTCTAGTATCCAGAT	51317
rs751476620	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46011311	CTGCCCAACATGGTA[A/C]AACCCTGTCTCTACT	51317
rs751524506	snp	C/G	1.80052e-05	0.00300038	intron-variant	PHF21A	GRCh38.p7	11:45945814	AAGCTCTCAGAAAGA[C/G]AGTGTGCTTTTCCCA	51317
rs751530062	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46062951	GGACTGGATTGACAG[A/T]AGGATGAGCGAGACG	51317
rs751530482	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931019	TGAGTGCAGAATGTA[A/G]GTTTGGGGGCTGGGT	51317
rs751536501	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46046573	AGAAGCCATTCTAAG[A/G]CAATCTCACAGAGGC	51317
rs751551633	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46057060	CACACAAAAAATATT[A/T]TTGACATTAATCTGT	51317
rs751580003	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45934417	AGGGCGGGTGGAGTG[A/G]GTAGGCTGGGGGGTC	51317
rs751598787	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46038464	ATTTATTGAGCACCT[C/G]CATGTGCTACATACT	51317
rs751598879	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45987660	GCAAGACCCCGTCTC[-/AA]AAAAAAAAAAAAAAA	51317
rs751621286	snp	G/T	9.89674e-05	0.00703377	intron-variant	PHF21A	GRCh38.p7	11:46084140	TACTTAACAACAGTG[G/T]GGGAGAAGCCAATAA	51317
rs751635128	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46073541	AAAATATACATAAGA[A/G]TATACAGAAAAAATA	51317
rs751642081	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45986840	AATTATATTTCAATC[A/G]CTTGATTTTTAACAT	51317
rs751722849	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46090436	AGGATAAGAGTCGTA[C/T]AAAAAAGGAATGGGT	51317
rs751748943	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45999937	GTGCTAAGAGAAAGT[C/T]GCAATATTCTGCAAG	51317
rs751755568	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016779	AGCCCTCAGAAATGT[C/T]TGGTAAACTGAACTG	51317
rs751774307	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46050987	AATATAGCAGTCTCC[A/G]AGTTCTCTGTGCCAT	51317
rs751783486	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46105083	CCTCATAACCACTTC[A/G]TTTTATTCAAATTTT	51317
rs751790364	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45946835	TATGAGGGTGGAGAC[C/T]GGCAAAGCAAGGAGG	51317
rs751798628	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46088810	GACTGTAGGCTTTTC[C/T]GTTCTCAAATTCTCT	51317
rs751808135	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46065673	CTCAGAGAAATTCAA[A/T]GGACACAAAGCCTGT	51317
rs751839230	snp	C/T	1.64841e-05	0.00287085	synonymous-codon, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934160	AATCAGCTGTTTTAC[C/T]TTCTCCAGGGAGCTG	51317
rs751840265	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45967368	GTGAGACCCTGTCTT[-/AA]AAAAAAAAAAAAAAA	51317
rs751855492	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016689	TGTTTTTCTCCTCTA[C/T]TATACTGCCAGCACC	51317
rs751860563	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46050016	GTCACCACATGTTCA[A/G]TTTGCTGTAGGGCTC	51317
rs751930327	snp	A/G	1.64749e-05	0.00287005	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971223	GCACATCAGTGCTGA[A/G]CACAGCCTTCTGACT	51317
rs751939079	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46014335	CATGTTGCTGCAAAG[A/G]ATATTATGTTGTTCT	51317
rs751948120	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46064588	ACCATAAAAAGATAC[C/T]AGTTAAAGAGTAAAC	51317
rs751974946	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46069517	AGAGGCTGGAGATAG[C/T]CATATATCAGGTAAC	51317
rs751981172	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46034211	GAGTTGCCTTAATAT[A/T]AGTGCCCCCACCCCC	51317
rs751988938	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46105477	TTCTCCACACTCAGA[-/C]CCACACTAACCAGGA	51317
rs752001261	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46067856	AGTACCACAATGAGC[C/G]CCAAATAAAGTAGGC	51317
rs752016931	in-del	-/AAAA	0.38637	0.209531	intron-variant	PHF21A	GRCh38.p7	11:45935742	TCTTCTTCTTTTGCT[-/AAAA]AAAAAAAAAAAAAAA	51317
rs752027015	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46029987	TTGATTTGATAAATA[C/T]CCTCCTCACTCAAAT	51317
rs752035023	snp	C/G	4.9423e-05	0.00497082	intron-variant	PHF21A	GRCh38.p7	11:45948848	ACACACAAAGCAAAA[C/G]CAACAGCAGCAAGGG	51317
rs752069857	in-del	-/A	1.80686e-05	0.00300566	intron-variant	PHF21A	GRCh38.p7	11:45971412	CACTAAATCTAAACT[-/A]AATAATAAACTAAAT	51317
rs752078877	snp	C/T	3.30246e-05	0.0040634	intron-variant	PHF21A	GRCh38.p7	11:46079205	GCCATCAGTCTTACA[C/T]ATTAACTCCCTATGG	51317
rs752087890	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45993070	TCCAACCAGAACACT[A/G]AAACTAACATCTTTT	51317
rs752111715	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042710	TAGGTCACGAGGGCC[C/T]TCCTTCACAAATGAG	51317
rs752112861	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46028930	ATGTGTATTACTATG[A/C]CCCAAAGGACTATAT	51317
rs752135584	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45994137	TGCTAACCTTACAGC[C/T]TCAAGCCAAAAACTT	51317
rs752190000	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45976603	TCCCAACACTGTGGG[A/T]GACCGAGATGGGTGG	51317
rs752198646	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46080273	AAGTTATCCTTCCAC[C/T]TCAGCCTCCCGAGTG	51317
rs752198995	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042953	GGTATTTTGTTATAG[C/T]AGCCTGAATGAACTA	51317
rs752213589	snp	C/T	1.70609e-05	0.00292065	downstream-variant-500B, stop-gained, synonymous-codon, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928819	CTCCCAGCCCTGCAG[C/T]AGCCCCAGAGCCCTG	51317
rs752213799	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46044034	CTGTAAATTTGTTTT[C/T]ACCTTCATAGAGTAA	51317
rs752215628	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46001408	GTACTTAGCCAATGC[A/G]CCTGTAGATTCTAAT	51317
rs752225934	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46008075	TGAAAATTAACACGA[A/C]GTGAAGTTCAGAAAG	51317
rs752232127	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46112918	TATATTATTTTGTGT[A/G]TAAACCTTATAGTAG	51317
rs752233590	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45966305	CTCATCAATTTCTTC[C/T]TCCAATCTTCTCTTC	51317
rs752263783	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:46032842	CCATTAATGATTTTA[-/AT]ATGTTTAATGATTCA	51317
rs752277085	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46114574	GTCAATACAACATAC[C/T]GTCCATAAGGCCAGA	51317
rs752278112	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45993316	GTAATCACATATTTA[C/T]ACAGCACTTTACGAT	51317
rs752305378	in-del	-/TAAACTA			intron-variant	PHF21A	GRCh38.p7	11:46080531	ATTATATTAATATAC[-/TAAACTA]TAAACAATAGGTTCC	51317
rs752332956	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46058444	CAGGAACTTAGTCTT[A/G]TAGGACTGATATATT	51317
rs752378703	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46095055	GGCTTTAATTGGTTT[C/G]ACAATGAGGTTCACA	51317
rs752420937	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46072080	TTCCCTGACTTCCTG[A/G]AACTAACAATCTAAT	51317
rs752421334	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46024086	ATTGGTTATGAAAGC[A/C]AGGAAAGGGCAAGGT	51317
rs752422069	snp	A/G	3.36729e-05	0.00410308	intron-variant	PHF21A	GRCh38.p7	11:46076852	ATATCTGTGAGAAAG[A/G]TATTTCATTTGTTAA	51317
rs752422990	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46057520	TATAAAGGGAAAAAC[C/T]GTACTTTCTGTTCTC	51317
rs752426464	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46031556	AGTAGTTCATGCAGC[C/T]GGTACGAATTCATTC	51317
rs752463587	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46110715	CTTATAAAGTAGAAG[A/C]ATATCAGACCAGATT	51317
rs752471083	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933640	AAACAGAAACAAACC[C/T]ATCGTGGCTGTGGAG	51317
rs752512926	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46070716	CTATCTCTCTAAAAA[C/G]GAGTAAAAAGAAATA	51317
rs752524844	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45984673	GACTGCCCCCACCCA[A/G]TCAACCCACCAGTTT	51317
rs752540362	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45944581	ACCCTGGCCAGCTTG[C/T]TCTGCCCCCGCTATC	51317
rs752547598	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46020331	CTGAAGTGGCTGCTA[C/G]TATCCTGCAGCAAAC	51317
rs752548665	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46086777	TAACATAAAACCATA[C/G]TTCAATTCAATTCAC	51317
rs752557278	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46088360	TTGCAATCTTCCAAA[C/T]GGTACATGTCAAACC	51317
rs752583357	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46049701	AGCCGCTGTCCTACT[C/T]AGGGGGTCCCCTCCA	51317
rs752601368	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46035732	TGGGGAGGAGAACAG[C/T]GTCTCAGAAGGGAGA	51317
rs752614428	in-del	-/AGCCT			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932147	AGGGCTGATGCAGCC[-/AGCCT]AGCCTGTACTCCCGC	51317
rs752635361	snp	A/T			synonymous-codon, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934055	GGTGGCGGCATTGGC[A/T]GGGGGGGTGCAGTCC	51317
rs752662117	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45998504	CATGCAAAATAACTC[C/T]ACCATTTCTTTTTCT	51317
rs752695673	snp	C/T	3.43383e-05	0.00414343	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965509	TGGGGGTGAACTTGG[C/T]CAGCATGACGGGCCT	51317
rs752721147	snp	A/G	1.65625e-05	0.00287766	intron-variant	PHF21A	GRCh38.p7	11:46076711	GCAGACATATCTTTA[A/G]AACACAACGTTAAAA	51317
rs752745939	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46014872	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	51317
rs752788110	in-del	-/CTCTCT/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PHF21A	GRCh38.p7	11:46121165	TCCTCCTCTCCTCTC[-/CTCTCT/T]CTCTCTCTCTCACTC	51317
rs752817042	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45973130	AATTAAATGTAATTA[A/G]TTAAAACAAAAACAA	51317
rs752834981	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46073930	CCTTCCAACCAAGAA[C/T]TCAGTGAAATTCACT	51317
rs752837908	snp	C/T	1.64784e-05	0.00287035	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938256	GGAACATGTGTCGCA[C/T]ATCAGTAACTGGCCA	51317
rs752845361	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46075456	AGCGCTAACAGAATT[C/G]TAAAGCTAGAACACT	51317
rs752890173	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45987376	ACCATAAAAAAGCAC[C/T]TGAGGCCAGGCGTGG	51317
rs752901378	snp	A/G			downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929146	CTCTGGGGCTAGGGC[A/G]TCAGTGCACAAGGGA	51317
rs752903995	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46039771	CAGGATCTCAGTCAA[A/C]ACTGCACAATCTGCA	51317
rs752904893	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45988719	CATGGCAAAAATCCC[A/G]TCTCTACAGAAAATA	51317
rs752906799	snp	A/G	1.64863e-05	0.00287104	intron-variant	PHF21A	GRCh38.p7	11:46084160	GAAGCCAATAATACA[A/G]CTTACCTGGTGAACC	51317
rs752935762	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46091983	ACATGCAGGCCTAGC[G/T]GTATTAGCAGAAACA	51317
rs752969599	snp	A/G	1.64895e-05	0.00287132	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934177	TCTCCAGGGAGCTGT[A/G]CATCTCCTTCTGCCG	51317
rs752978752	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46106931	TTCACAGAAAGAAAG[A/G]CTGTTTCTTTAAAAT	51317
rs753047910	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45944496	GTAATGGTCTCCCAT[C/T]TTACTGAGAACGAAA	51317
rs753051511	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46067328	GTATGTATGAGTTCA[A/G]TGGGGAGGCGGGCAT	51317
rs753058630	snp	C/G			missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965478	TGGATGGAATTCTGG[C/G]ATGTGGGAAGGGTTG	51317
rs753066631	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46105363	CATGTGTGCCAGACG[C/T]CTTTACAGGCACACA	51317
rs753075835	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46017989	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	51317
rs753086590	snp	C/T	1.64743e-05	0.00287	intron-variant	PHF21A	GRCh38.p7	11:45949370	AATAAAACTGGAACA[C/T]GAGGGAAGGGCCAGA	51317
rs753091988	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46001648	CATTTTTAAAATTCC[A/G]TTAGTATCTTGCCAG	51317
rs753096501	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978259	TGAGCCAAGACTGCG[C/T]CACTGCACTCCAGCC	51317
rs753105422	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45946888	TATCCCTTGCTTTTA[A/G]AGCTATTGAGAGGCA	51317
rs753105898	in-del	-/CACT			intron-variant	PHF21A	GRCh38.p7	11:46099976	TTGATCCTTTCTCAC[-/CACT]GCTATCCTTAATGAA	51317
rs753110002	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46064605	GTTAAAGAGTAAACT[C/T]CTTTTTCCTGTCTGG	51317
rs753149724	in-del	-/AAATCTGAACTCCATTTAAGTAACTTCTGTTTCTCTTCTTCTTTTGC	1.64901e-05	0.00287137	splice-acceptor-variant	PHF21A	GRCh38.p7	11:45935694	TCTCGTTCTTGTTTT[lengthTooLong]TAAAAAAAAAAAAAA	51317
rs753159036	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46098009	TCCCCCAAAAGATTC[-/T]TAATAGGGAGCCAGG	51317
rs753169487	in-del	-/AAGA			intron-variant	PHF21A	GRCh38.p7	11:45957722	CTAACTTTACACCTT[-/AAGA]AACAGAAAAAGAACT	51317
rs753183759	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016766	CCTGGAGCTTGGCAG[C/T]CCTCAGAAATGTTTG	51317
rs753197489	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46096720	GAACTCTTCCCCTTA[C/G]GTGATCTCACACAGT	51317
rs753208477	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:46015991	ACACATAAACTGATA[-/AC]ACAGTCATTTATTAT	51317
rs753228175	in-del	-/GAG			intron-variant	PHF21A	GRCh38.p7	11:46103962	AAACTCCTCAAATCT[-/GAG]GAGATCATTGTACCT	51317
rs753240794	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978072	TTTGGGAGGCCGAGG[C/T]GGGCAGACCACGAGG	51317
rs753244051	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46065794	AGCGGGTGTATAAGG[G/T]TGAAGGGATCACAGT	51317
rs753247469	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45937762	CTGAGATTACAGGCC[C/T]GAGTCACCACGCCTG	51317
rs753258099	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016988	TTTTTTTTTTTTAAT[C/T]GAGATGGAGTCTCAC	51317
rs753274470	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45979347	AAATGCTTCTTTCTA[G/T]CTGGTCCCAAGAGCA	51317
rs753309318	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46081826	ACTCATTCATTTATA[G/T]ATTGTCCGTGGCTGT	51317
rs753318547	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46032867	TGATTCATACAAGAG[C/T]ATAAGTACATGTGTG	51317
rs753330592	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46067877	TAAAGTAGGCACAAG[C/T]ACCAAGTACCATGAG	51317
rs753337160	snp	G/T	1.64743e-05	0.00287	intron-variant	PHF21A	GRCh38.p7	11:45979747	GCCTGCAATGTTCCA[G/T]CCACACATTTACCTG	51317
rs753350908	snp	A/G	0.000293315	0.0121067	downstream-variant-500B, utr-variant-3-prime, synonymous-codon	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928861	GGCTGGGCCGGCGCT[A/G]CCCCTCATCTTAGCA	51317
rs753366255	in-del	-/GT			intron-variant	PHF21A	GRCh38.p7	11:46064324	CGAGCAGGAGAAAAG[-/GT]GACAACTGAACAGAT	51317
rs753366425	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45996274	ATCCTATTAAAAACA[C/T]AGGATCTAGTACTCA	51317
rs753406865	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46031780	ATTTTTTTCCAGAGA[A/C]GTTACTAACACTATA	51317
rs753446335	in-del	-/AG	2.61141e-05	0.00361336	intron-variant	PHF21A	GRCh38.p7	11:45969932	GAAGATAAATAAACC[-/AG]AGAGAACAATTACTC	51317
rs753454505	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46017577	AGGATTTGCCCTTAA[-/G]GGGGGAAAAAAAAAA	51317
rs753466737	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45978230	GTTTGAACCCAAGAC[A/G]GTGGAGGTTGCAGTG	51317
rs753502294	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45939202	ATTAACATTATAGGC[A/G]ATACCTAAGAGTTTT	51317
rs753508553	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46080628	CAGTCCACTCCTTAA[C/T]GTCAAGTAGTCAGCC	51317
rs753517625	snp	C/T			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934850	TGCTGGCTTCTATTT[C/T]AGGCAGGGAAAGAGA	51317
rs753542180	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46017313	TTTGCTATCTTCTCA[C/T]AGTTCTAGCAAAGGA	51317
rs753543756	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46114236	AGCTATCAGTAACAC[A/G]TCCAAACACAAGCTG	51317
rs753545133	snp	C/G	3.45072e-05	0.0041536	downstream-variant-500B, missense, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928827	CCTGCAGCAGCCCCA[C/G]AGCCCTGCCCGAGGC	51317
rs753558110	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46060751	AGTTTGCAAACATTT[C/T]CTCCCATTCTGTAGG	51317
rs753565452	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46009859	CATCTGGTATAACTC[C/T]TTCATCACCTTGCAT	51317
rs753576258	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45955390	GACATTTTAAAGTCC[C/T]GGATGCCCAGAAATC	51317
rs753582517	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46097175	TTCTACCCTAGCCCC[A/G]CTAAGGTATATTCTC	51317
rs753612232	in-del	-/AG			intron-variant	PHF21A	GRCh38.p7	11:46073869	ACTTTGAAATCTGCC[-/AG]AGTTTCTTTCAGAAA	51317
rs753622476	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46058789	TCTCTTTACAAAATC[C/T]GGAACAAGAACAAGC	51317
rs753631848	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46112748	TTACGGAACAACTAT[C/T]CCCATTTTAAAAAAA	51317
rs753644110	snp	C/G	1.71481e-05	0.0029281	intron-variant	PHF21A	GRCh38.p7	11:45938119	GGCCGTGTCTTTGTC[C/G]TCCTCGGCCCCTCCC	51317
rs753654604	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46008347	CTGTGAAGCATATCC[A/G]GGACACTATGGACCA	51317
rs753660283	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45969455	GCTGTTGTTTCCTTC[C/T]CTACTCTTTTTGGCA	51317
rs753664675	snp	C/T	3.30726e-05	0.00406635	intron-variant	PHF21A	GRCh38.p7	11:45936447	TGCCAGTATTTTTTT[C/T]AAACAAGGGGAAGCT	51317
rs753692133	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46083695	AGCTTTTTGTAAAAT[A/G]TAAGAATTGTGAAAT	51317
rs753706815	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46081500	CACTGGAATTTAAAA[A/C]TTCACTGATAACCAC	51317
rs753712133	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46073223	GTCCCAGCTACTTGG[G/T]AGGCTGAAGTGGGAG	51317
rs753721014	snp	G/T	1.69726e-05	0.00291308	intron-variant	PHF21A	GRCh38.p7	11:46076861	AGAAAGATATTTCAT[G/T]TGTTAACAGAATAGT	51317
rs753757359	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46080167	TTTATCTAACTACTA[-/G]TTTTTTTTTGAGACA	51317
rs753758211	in-del	AATATTTTTCCCCCTCATGTTATTTA/CTATATTGCTCAG			intron-variant	PHF21A	GRCh38.p7	11:45981420	AAAAAAAAAAAAAAA[lengthTooLong]TAAATGTCCTTGTTC	51317
rs753776131	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45984083	TTATCCTGAAGCTTT[-/C]GAGAAAGGGCTAAAT	51317
rs753782589	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46000386	AGATATGATAGTACT[C/T]ATAGCACTTCTGAAT	51317
rs753813818	in-del	-/AAAT			intron-variant	PHF21A	GRCh38.p7	11:46111479	GACTCCGTCTCAAAT[-/AAAT]AAATAAATAAATAAA	51317
rs753842741	snp	A/G	1.67449e-05	0.00289347	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945864	GGTGGGGCTGGGCAG[A/G]GACACAGGCTGAACA	51317
rs753842887	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46023103	TCAGACCTTGAGTGA[C/T]ATGTGGACAATCTGG	51317
rs753892419	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997626	TAAATGCTTGTTTTG[C/T]AGCCTTAAAAGTGGC	51317
rs753922676	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46048273	TAAGGCCTTTTGTCA[C/T]TGGCTTCTTTTACTT	51317
rs753974876	snp	C/T	1.78912e-05	0.00299086	synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933983	TTATTTAGTCTCTTC[C/T]CCCTGGTTACAGTTC	51317
rs753991831	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46090423	AAAGGAAGAACTAAG[A/G]ATAAGAGTCGTACAA	51317
rs754042061	in-del	-/ATAA			intron-variant	PHF21A	GRCh38.p7	11:46108584	TATATATATATATAT[-/ATAA]ATAAAATACATATGT	51317
rs754043511	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45989119	AATTACTGATTAACT[G/T]CATGGAATTGGCTCT	51317
rs754050644	in-del	-/AG			intron-variant	PHF21A	GRCh38.p7	11:46117329	TCACCTAACACTAAC[-/AG]AGTTTCAAAGGACCA	51317
rs754056660	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45974648	TTAGTAGAGACGTGA[G/T]CTCGCTATGTTGCCC	51317
rs754067061	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46116301	CCTAATACTAACACA[C/T]ACAGATATACATCTT	51317
rs754092724	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46075719	TGGAAGATGATTCTA[C/T]TCTGAAACATTAATG	51317
rs754100665	in-del	-/AG			intron-variant	PHF21A	GRCh38.p7	11:46035815	TTAGAGTTTGAAGAA[-/AG]AGAGAGAGAGAAAAG	51317
rs754107724	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46106922	CTTCAGCCTTTCACA[A/G]AAAGAAAGGCTGTTT	51317
rs754136407	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46104096	CATCAGGCACCAAAT[C/G]AGAGGAAATTTCACA	51317
rs754138626	in-del	-/GAAAAA			intron-variant, cds-indel, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119744	CGAACGTGGTCAGGG[-/GAAAAA]AAAAAAAAAGAAATC	51317
rs754141020	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093321	CCAATAGTGTCTCAT[C/T]GCCTCAGGGAATATT	51317
rs754182092	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45977640	ATCCTCTAAACATTC[C/T]TTCAGAACTAATACA	51317
rs754200680	snp	C/T	1.88677e-05	0.0030714	intron-variant	PHF21A	GRCh38.p7	11:45935554	GAAACAGCCTGGGGC[C/T]CACACGTACTGTTAC	51317
rs754208279	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45949971	CCTAAATGAACAGAA[A/G]TCACCTGAATTTAGG	51317
rs754235811	snp	A/T	1.64806e-05	0.00287054	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979864	GTTGCTGCTGTGCTG[A/T]TTGTAGTTTGTTTTC	51317
rs754271839	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45975767	AAAGCAAACTGTTCC[C/G]ATTCCCTCTCCCAAA	51317
rs754277810	snp	A/G	1.64735e-05	0.00286993	intron-variant	PHF21A	GRCh38.p7	11:45949378	TGGAACATGAGGGAA[A/G]GGCCAGATGCTGGCC	51317
rs754306121	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46054817	CTGAATGAATTAAAT[A/G]TTGAAAGATTACCTT	51317
rs754316971	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46107045	TCTGCAGGAAGAATG[A/G]CCTATCTTGAGCACT	51317
rs754325904	snp	C/T	0.000185477	0.0096283	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935083	TGCAAATACAACCCT[C/T]TTTCCCACTTGGACA	51317
rs754336032	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46039454	GGGGAAGCCTGAGAA[C/T]AGTCAGGTAAGTACA	51317
rs754367741	snp	C/T	1.66269e-05	0.00288326	intron-variant	PHF21A	GRCh38.p7	11:45950156	CATCATTTTCAGGAA[C/T]AAAGCTGTGGGCCAG	51317
rs754381433	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46068704	TCCAGTCAGTAGATT[A/C]TAGTAGCCCAGTGTC	51317
rs754393987	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46053214	TCACATCTCTCATGG[A/G]TAGCAGAATAAAACA	51317
rs754419864	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45937634	TACAGGCGCCTGCCA[C/T]CATGCCCGGCTAATT	51317
rs754433333	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45993085	GAAACTAACATCTTT[G/T]ACATTTAACTGGTTC	51317
rs754500229	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45997640	GCAGCCTTAAAAGTG[G/T]CAGACAAATTAAAAT	51317
rs754509507	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46077435	TGAGATACACAGAGC[A/T]TGATTGCCTTTTACT	51317
rs754525806	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46006487	ACCTCCACAAATCAC[A/G]CTATATAAATAACAA	51317
rs754611272	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46057434	ACAGATGCCCAGAGC[A/T]TTAGGGCTTAATTTT	51317
rs754615406	snp	C/T	1.7501e-05	0.00295807	intron-variant	PHF21A	GRCh38.p7	11:45935575	GTACTGTTACGTATA[C/T]TGGAAAGGCCTAGGT	51317
rs754615899	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005305	AAATGATGTAAAATA[C/T]TGTATAAAATTTATA	51317
rs754621014	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46110453	TGGCTGCCCAGTTTT[A/G]CTCTCCTTATTTCCT	51317
rs754622691	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093968	GGACAAAATTAAAAT[C/T]AAGAACTTCTGCTCA	51317
rs754661538	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45993921	AAACTGCTCTAAGTA[C/T]TTGGAAAGGCTGGGA	51317
rs754665435	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46020988	TTTCAATGTATGATG[G/T]GTTTATTGGACCATA	51317
rs754708897	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46108890	CTATTAGACCCCACC[C/G]CATGCTACGCACTAT	51317
rs754720020	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46052168	GCTCTATGCTGGTAC[C/T]TCCAGGAAAAAACAA	51317
rs754727403	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46064531	GGGAAACATATCTTC[C/T]GAAAACATAATTTTG	51317
rs754758566	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46069100	CAGTCACACTACATA[C/T]ATACAACCTCTCGAT	51317
rs754760188	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46017549	AAGAGCTCCATATTT[A/G]TAAGTTACAGTTCAG	51317
rs754829369	snp	A/C	0.000148604	0.00861859	intron-variant	PHF21A	GRCh38.p7	11:45950196	CAGTGCCAAGAATAT[A/C]TTCTCTTACCTTCTA	51317
rs754833209	snp	C/T	3.31082e-05	0.00406854	intron-variant	PHF21A	GRCh38.p7	11:46076709	GAGCAGACATATCTT[C/T]AGAACACAACGTTAA	51317
rs754848115	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45981090	CTATACTCTGCACTT[A/G]TAACTATATTGCTGG	51317
rs754850902	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45984152	TGAGAGTTAAAAGAG[-/A]GGGAAAAAATCAGGG	51317
rs754856822	snp	A/G	2.48407e-05	0.00352416	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928893	TGGGCAGACACCAGG[A/G]CAACCTGCCCTCCGC	51317
rs754873508	snp	A/G	1.70069e-05	0.00291602	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945850	CTTACGTCTGTGGAG[A/G]TGGGGCTGGGCAGGG	51317
rs754885588	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46048928	TTCAAGTGGCTGTAA[C/T]ATTTTACATTCCCAC	51317
rs754888300	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45963148	CTGGGGGCCGGGTGC[C/G]GTGGCTCACACCTGT	51317
rs754890625	snp	G/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931181	TCAATTCCTAGCCCC[G/T]TCCTCCGACCCAAGA	51317
rs754911690	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46033286	ATTGTTGTTGTTGAG[A/G]CACAGTCTTACTCTG	51317
rs754933765	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46082510	TAAAATATTATTGAC[A/G]TATAAATAAATGTTT	51317
rs754936395	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46048181	AATTCCCCCAGCCCT[A/G]GGCAACCATTAATTG	51317
rs754937092	in-del	-/TTTTTTTTTTTT			intron-variant	PHF21A	GRCh38.p7	11:45981950	TTTTCTTTTTTTTTT[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTT	51317
rs754944318	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46008788	ATAAATGTAAATTCA[A/T]CTGCAAAATGCTATG	51317
rs754945730	snp	G/T	3.60568e-05	0.00424583	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933964	TTCTCCTAGAGGGGC[G/T]CTGTTATTTAGTCTC	51317
rs754965971	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46099872	TAGCTCCACAACACA[A/G]ATAAAAAAGAACCCT	51317
rs754974481	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46081689	AGTTAGGTTACTTTC[C/T]GCCAGAATGCGGCAA	51317
rs755013485	in-del	-/ACA	1.65551e-05	0.00287702	intron-variant	PHF21A	GRCh38.p7	11:46076715	ACATATCTTTAGAAC[-/ACA]ACGTTAAAAATATGC	51317
rs755014892	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46025784	AATTATTTGCAAGTC[A/G]TAGGCATAATATGGC	51317
rs755022706	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46046594	TCACAGAGGCCTTTC[C/T]AATCATTTTGTGCAT	51317
rs755032513	snp	G/T	3.29511e-05	0.00405887	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979900	GTGGCAATGGCTGTA[G/T]TTGGAACTTGTCCGG	51317
rs755091215	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46090639	CCACAGAAGCCTTTT[C/T]CCACCCCCACCCCAC	51317
rs755097066	snp	G/T	1.68371e-05	0.00290143	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45969823	TACTCACCTGTGGAA[G/T]AAAGTTTGGACGTGG	51317
rs755168407	snp	G/T	4.93864e-05	0.00496898	intron-variant	PHF21A	GRCh38.p7	11:46079092	TTTATTTTAAATTAT[G/T]TTTAAATTTAACAAT	51317
rs755203223	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45935743	CTTCTTCTTTTGCTA[-/AA]AAAAAAAAAAAAAAA	51317
rs755207356	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45989272	TTTAAATCATTAGTA[C/T]TACAAATCTTATTAA	51317
rs755214673	snp	A/G	1.64885e-05	0.00287123	synonymous-codon, stop-gained, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934175	CTTCTCCAGGGAGCT[A/G]TGCATCTCCTTCTGC	51317
rs755221012	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45985101	GATACTAAATTTTAC[A/G]CGTATGGAAAAACTA	51317
rs755243761	in-del	-/AG			intron-variant	PHF21A	GRCh38.p7	11:45951257	AAGACATACTCCTGT[-/AG]AGTTATTTATACCAC	51317
rs755248584	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46051123	TCTCTCTGAGGTAAA[A/G]TACACCACATTTAAA	51317
rs755258522	snp	A/G	2.26339e-05	0.00336399	intron-variant	PHF21A	GRCh38.p7	11:45965278	ATGCCTCAACGACAA[A/G]GCTACTGCCCAGAGC	51317
rs755269945	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45946868	AAATTCAAGTTAACT[A/G]TTCTTATCCCTTGCT	51317
rs755290812	snp	A/G	1.64912e-05	0.00287147	intron-variant	PHF21A	GRCh38.p7	11:46084143	TTAACAACAGTGTGG[A/G]AGAAGCCAATAATAC	51317
rs755338228	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46050077	AGTCTTTCCCCAGCA[C/G]AGTTAGCGATTGCCA	51317
rs755355368	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45961572	TATGAAAAATATTTA[C/T]GGTAACGTGGCAATT	51317
rs755359839	in-del	-/CACACACG			intron-variant	PHF21A	GRCh38.p7	11:46040928	ACACACACACACACA[-/CACACACG]CACGCACAATTAAGG	51317
rs755361616	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45945052	ACAGGCATAAGCCAC[C/T]ATGCCCGGCCCCATT	51317
rs755384870	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46065679	GAAATTCAATGGACA[C/G]AAAGCCTGTCAGTGA	51317
rs755410646	snp	G/T	0.00297611	0.0384603	missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934063	CATTGGCAGGGGGGG[G/T]GCAGTCCGGGCCATT	51317
rs755420063	snp	G/T			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122604	GGAATCGGCCACGTA[G/T]AATCCGGCGGTTTGT	51317
rs755441106	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45976528	CCAGAATCTACCACA[C/T]AGATTGGTAGTACCA	51317
rs755474903	snp	C/T	3.25061e-05	0.00403137	intron-variant	PHF21A	GRCh38.p7	11:45969948	GAGAGAACAATTACT[C/T]TTCAATATCAAAGCT	51317
rs755494283	snp	A/C	1.64743e-05	0.00287	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971233	GCTGAGCACAGCCTT[A/C]TGACTGTTGATGGCG	51317
rs755499268	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45975775	CTGTTCCCATTCCCT[A/C]TCCCAAAAAGAATTC	51317
rs755511499	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46117849	CGCAATCGCACATCT[A/G]CTTTGTACAGTCAAA	51317
rs755515889	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46013358	ACTTAGTAGCTATCT[C/T]GGTTATCAGATCAAC	51317
rs755516849	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46009550	CAAGCACAGTTCTAA[A/G]CACGCTATGTATTAC	51317
rs755518003	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46029991	TTTGATAAATATCCT[C/T]CTCACTCAAATTTAT	51317
rs755552087	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:46097827	ATCTCCCTAACTAGA[-/AC]ACACACACACACATA	51317
rs755565783	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46056478	GAGCTAATATCACAG[C/T]GAAGATTTTAAAACA	51317
rs755567806	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46089700	TAATAATGTTGTTTC[C/T]TATGAAATAAAAAAA	51317
rs755580754	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45978092	AGACCACGAGGTCAG[C/G]AGTTCGAGACCAGCC	51317
rs755598735	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45939302	GTTTCACAATATGAT[A/G]CAAACAATTCTCATC	51317
rs755606438	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46029060	TCTGACCATTACCTT[C/T]TCAAAACAAAATGTA	51317
rs755607284	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46001772	CACAGGGCTGTCACT[-/C]GTACTAGAAAAACGT	51317
rs755636877	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46064999	TTATAACTTCATGGT[A/C]TTTCAGCATGCATAT	51317
rs755644594	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971256	TGATGGCGGTCACCA[C/T]AGCAATGGTAGGTCT	51317
rs755645837	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46028379	TACAGGCAATTCTCA[C/T]TTTGCTGAACTGGCT	51317
rs755673375	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46030252	TTTTAGTTTCTATTC[C/T]GATTTCTTTAAAAGG	51317
rs755689332	in-del	-/TGAACCCACAT			intron-variant	PHF21A	GRCh38.p7	11:46063831	TACTGTTTCATCTGA[-/TGAACCCACAT]TGAACCCACATCATA	51317
rs755699822	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45994313	TGATTCACTAACAGA[C/T]TTATCTTACTGCCAT	51317
rs755715062	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45993372	AATAAGACTCTCAGA[A/T]CTGTGCAGGGCTAAT	51317
rs755768538	in-del	-/AAA			intron-variant	PHF21A	GRCh38.p7	11:45935742	TCTTCTTCTTTTGCT[-/AAA]AAAAAAAAAAAAAAA	51317
rs755808954	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46006784	CTACAATAAAAATGG[C/T]ACAAAAATATTTTAA	51317
rs755822359	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042239	TGACAAAACATATTC[C/T]TCAATAAGGCATATT	51317
rs755829269	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45969383	CCTTTAAGCATGATT[C/T]TCAAAACCATCACTT	51317
rs755830357	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46058604	TAATAAAATGACTGA[A/C]CCTAAACATGGACAG	51317
rs755846719	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45953777	GTATTATAGATTTCA[C/T]TGGGGGAGGGGAAAC	51317
rs755857049	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46095249	CAGCAAAAAGCAAGA[C/T]CTATACACACGTTTG	51317
rs755912918	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933712	TATATTATTTCACTT[A/G]GCATGGTGCTGGCAA	51317
rs755937141	in-del	-/CT			intron-variant	PHF21A	GRCh38.p7	11:46062701	GTGGAGCAGCTAGAA[-/CT]CTCTCATACACTACT	51317
rs755954176	snp	A/G	2.29613e-05	0.00338823	intron-variant	PHF21A	GRCh38.p7	11:45953646	AGAGAAAAATTAAAT[A/G]AAAATTCAGAATTCG	51317
rs755967510	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45942989	TAGGCCAAAAACTTT[-/G]GTTTTCTCCTTGACC	51317
rs755970576	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005354	CAGAAGTGTTTCAGA[C/T]TTTGAGATTTTTCAG	51317
rs755983333	snp	A/G	1.65471e-05	0.00287633	intron-variant	PHF21A	GRCh38.p7	11:46076712	CAGACATATCTTTAG[A/G]ACACAACGTTAAAAA	51317
rs755989673	snp	C/T	1.69464e-05	0.00291083	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935728	GTAACTTCTGTTTCT[C/T]TTCTTCTTTTGCTAA	51317
rs755996940	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46109014	CTCAACCTAACCCAA[A/C]CAAAATCAACATGAA	51317
rs756005968	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46023033	TGAGATTATGGGCAT[A/G]AGCCACCGCGCCCGG	51317
rs756015733	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45993560	AAAAGCTGGAGCTCA[A/T]TTTTCTGAGCCAACT	51317
rs756072384	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45997218	GTATGAAACAGAGGG[A/G]TTTTTTTCCATGAAT	51317
rs756076448	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45983200	TGCATTCACAACTGC[C/T]CCTCCCCCAGGGCCT	51317
rs756114307	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45957980	GGATTATAGGAGAAT[A/G]TATTGAAAAACTGTA	51317
rs756144454	snp	C/T	1.69026e-05	0.00290706	intron-variant	PHF21A	GRCh38.p7	11:46076855	TCTGTGAGAAAGATA[C/T]TTCATTTGTTAACAG	51317
rs756187278	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46034977	ACAGAGTTAGCCTAC[C/T]GTAGTTAAAAATGAA	51317
rs756189644	snp	A/C/T			intron-variant	PHF21A	GRCh38.p7	11:46116057	ATTTAAGATACTATA[A/C/T]CTTTTGATAGGCTCA	51317
rs756191238	snp	G/T	3.46045e-05	0.00415945	intron-variant	PHF21A	GRCh38.p7	11:45953497	CCATACACCATAGAC[G/T]GAGACCTGCCTTTGG	51317
rs756203063	snp	G/T	1.64923e-05	0.00287156	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938276	GTAACTGGCCACTTT[G/T]TCTGCAAACGCTGCA	51317
rs756204583	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45973154	AAAACAAAATTAAAA[C/T]ATCAGCTCCTCAGTT	51317
rs756206692	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46114570	CTTCGTCAATACAAC[A/G]TACTGTCCATAAGGC	51317
rs756225383	in-del	-/TG			intron-variant	PHF21A	GRCh38.p7	11:46021548	ATGTGTGTGTGCATG[-/TG]TGTGTGTGTGTTCAG	51317
rs756234189	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46099900	CCTGACTTTAGGCCT[-/A]AAAACTAAAAATGGT	51317
rs756251608	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46075522	GAATCACATTCAGAG[C/T]CAAATACATACTAAC	51317
rs756251798	snp	C/G			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929392	TCAGCTGCTCTGTAT[C/G]CCCCCCCACCCCCTC	51317
rs756276994	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46062141	CTTTTATTCTTGTTT[G/T]GCTAAAGTTTCACCA	51317
rs756280111	in-del	-/AAAC			intron-variant	PHF21A	GRCh38.p7	11:45985909	TTATATAGTACAAAT[-/AAAC]AAATTGACAACAGCA	51317
rs756289319	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45950698	ACATCTTCTTTCTCA[A/G]TGACAGAAATCAGTA	51317
rs756309278	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46026017	ACAATGTCCCAAGAA[C/T]GTCCTTTAAGTAAAA	51317
rs756337280	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46112191	GAGAAACTGAGGTGC[-/A]AGGACATTTTACACA	51317
rs756363310	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45971669	AATGGGGTAGGTATA[C/G]AGATACAGAATGTGA	51317
rs756366730	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46060919	GTATTGCTGAGGTTA[C/T]CTACCAGGGTTTTTA	51317
rs756369283	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45983067	AACAGAAGGGAACAG[C/T]AGGGAAAGCAGGAGC	51317
rs756375264	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46103874	TACTGGTTTCACTTA[C/T]AAGATAGAGACATTC	51317
rs756397279	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46024810	ATCTCAAAAAAAAGA[A/T]AGAAAGAAAGAAAGA	51317
rs756406620	in-del	-/ATG			intron-variant	PHF21A	GRCh38.p7	11:46029100	AGAGTGTTATCTGTC[-/ATG]ATAAGCTAAACCTTG	51317
rs756408471	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46073950	TGAAATTCACTGAGT[G/T]TTAGTCATGAAGGAT	51317
rs756420499	in-del	-/GTA	1.64822e-05	0.00287068	cds-indel, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979834	ACTGCTGCTGTTGTT[-/GTA]GTTGCTGTAGTGGTT	51317
rs756441738	snp	A/T	1.73921e-05	0.00294885	intron-variant	PHF21A	GRCh38.p7	11:45934271	AGCCGCCTGGTTTCT[A/T]ACAGGCCTGGCAGCC	51317
rs756455768	snp	C/T	1.6489e-05	0.00287128	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084184	GTGAACCTGAATTTC[C/T]ACTTTAAGAGCCTCC	51317
rs756470160	snp	A/C			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123119	CCATAGGCATGAAAT[A/C]CAGTTTTTGCAGATA	51317
rs756473894	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45948559	TGTTCTGCTTAATGA[C/T]TCTCAAATGCTTCCT	51317
rs756482917	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46037919	AGGATCGCTTTTCTT[C/T]TGAAGCTCCTACTAT	51317
rs756500520	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46091023	TGATTATTTATTTTA[A/C]AAGGTTTAATGAGAG	51317
rs756509314	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46009115	GAGTAGCTGGGATTA[C/T]AGGCGTGCATCACCA	51317
rs756514838	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46053163	TAGAAGTTGATTTAG[C/T]GTCCTGATAAATGTT	51317
rs756528773	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46034495	TCCACACTCCAAGAT[-/A]AAAAAGAACAAAAAA	51317
rs756530288	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45936873	AACCACTCCCGACAG[C/T]TAGAACCACCAACAC	51317
rs756566365	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46016858	AAATTAAACAGACAC[A/G]ACCTCAACCAATGAT	51317
rs756589458	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46001688	AGAAAGGCTGTGTGC[A/C]TCAGAGTTAACTGGT	51317
rs756595582	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46005764	AATTAAGCTTCCATA[A/G]CTCAAGACGGATCAT	51317
rs756616581	snp	C/T	1.64746e-05	0.00287002	intron-variant	PHF21A	GRCh38.p7	11:45948871	AGCAAGGGAGAGATA[C/T]AAAAAGGTCCTCACC	51317
rs756619564	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46065827	ACAGAGGCTCACAAT[A/C]TAGAGAGGAAGAAAT	51317
rs756620205	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45937949	TTTCAAATACAAGGA[A/G]GCATCTATCCAGCTC	51317
rs756624123	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45963718	ATAATATTTAATAAC[C/G]TAAAATAGTGTTGTG	51317
rs756641322	snp	C/G/T	8.23676e-05	0.00641693	intron-variant	PHF21A	GRCh38.p7	11:45949374	AAACTGGAACATGAG[C/G/T]GAAGGGCCAGATGCT	51317
rs756653683	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46018949	TCAATGTATCATACC[A/G]TAAGCAGCAAGAACA	51317
rs756679419	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46000167	GAAGGCAGCAAACTA[C/T]AGAGAAGAAACCAAC	51317
rs756707290	snp	A/C	1.64955e-05	0.00287184	missense, stop-gained, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934184	GGAGCTGTGCATCTC[A/C]TTCTGCCGGGCCAGG	51317
rs756716094	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45965713	TGTTTAATACACTTA[C/T]TAATGTTCATTTTGG	51317
rs756734220	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46002034	TTTCATGAGAAAATA[C/T]AAAGAAAAGAGTGAC	51317
rs756764746	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46105765	AAAAAGCACTAGGCC[A/T]CTTTGAAAGACTCAA	51317
rs756772849	snp	A/G	1.64738e-05	0.00286995	intron-variant	PHF21A	GRCh38.p7	11:45949379	GGAACATGAGGGAAG[A/G]GCCAGATGCTGGCCA	51317
rs756837246	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46067910	CACAGAAGAGGAGTG[G/T]CTAACTCTGCTTGGA	51317
rs756844656	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45979358	TCTATCTGGTCCCAA[G/T]AGCACTGATCCTGGA	51317
rs756882574	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45939266	TAAATCTTACAGGTA[C/T]GGAAATCCATTCATC	51317
rs756912783	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:45989240	AGAATTTCAGAACAC[-/AT]ATTTGCTTTTGTTTG	51317
rs756916296	snp	C/T	3.29544e-05	0.00405908	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971295	CCACAGAGGCAGGCA[C/T]GGTCGCAGTTGCTGC	51317
rs756924104	snp	A/G			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934862	TTTTAGGCAGGGAAA[A/G]AGAGGAAAGAGGTGT	51317
rs756928809	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46066193	GGTAACAAAGGTAGT[C/T]TCTCTGGTAGAGGAG	51317
rs756930892	snp	C/G	1.75551e-05	0.00296264	downstream-variant-500B, missense, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928832	AGCAGCCCCAGAGCC[C/G]TGCCCGAGGCTGAGG	51317
rs756935067	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46088139	GCATCAAAAGAATTA[C/T]TGGCTACATTTGTAA	51317
rs756967811	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45996298	GTACTCAAGGTAGTA[A/G]AGCTTACAGGTTGAC	51317
rs756971060	snp	A/G	3.29457e-05	0.00405854	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45948895	CCTCACCTCTCTTCC[A/G]GGTCCCAGGGTGCAT	51317
rs756972612	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45955438	TGAATAGGAAGGAGA[A/G]AAGTATGATGGAGGA	51317
rs756974830	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46044552	ATGCAGGACTTCTCT[C/T]ACTCTTTCGGGCAAC	51317
rs756979639	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46097993	TAGATCTGTATTTAA[C/G]TTCCCCCAAAAGATT	51317
rs757025201	snp	C/G			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122594	GCAATCACTGGGAAT[C/G]GGCCACGTATAATCC	51317
rs757051738	in-del	-/AC			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933136	TTTTTTCCTTCCTGG[-/AC]ACACACATCCTTCTT	51317
rs757060658	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46043380	GTTTACCCACATCAT[C/G]ACCTTTATCAATACA	51317
rs757078384	snp	C/T	1.71402e-05	0.00292742	intron-variant	PHF21A	GRCh38.p7	11:45938121	CCGTGTCTTTGTCCT[C/T]CTCGGCCCCTCCCCT	51317
rs757083488	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45956014	GAAGGAAATGGGTTA[A/C]TATATTTAAAGTGCT	51317
rs757113475	snp	C/T	3.28294e-05	0.00405137	intron-variant	PHF21A	GRCh38.p7	11:45953667	TCAGAATTCGTTTTT[C/T]ATTAAAAGGATGAAG	51317
rs757135512	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45953987	CCCAGAAGCAAGCCT[A/G]CTATTTTTTGTTGTT	51317
rs757144111	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46024142	AATGATTTTATATGT[G/T]GGGCTAACTGAGTTG	51317
rs757166311	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46058840	CTAGAATGGAGAAGA[C/T]ACAAACATGGGAACT	51317
rs757184850	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45934495	ACACAGGAGTACTAA[C/T]GCTTAAAAACAAACC	51317
rs757202768	in-del	-/CT			intron-variant	PHF21A	GRCh38.p7	11:46027168	AGCTGTCTCACATCA[-/CT]CTGCTTTTTCTCCCT	51317
rs757237297	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46007001	AGCATATGCCACACA[C/T]TTCACAGTTTTAATC	51317
rs757243048	in-del	-/TAA			intron-variant	PHF21A	GRCh38.p7	11:46095678	TAAATCTAAAGCAAT[-/TAA]TAATTATTTAAATAC	51317
rs757254710	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45943367	AATGTTTTGTAGAGA[C/T]AGGGGTCTTGCCATG	51317
rs757254970	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46014989	CGTCTCAAAAAAAAA[A/T]AAAAATAAAAATAAA	51317
rs757274628	snp	G/T	1.69355e-05	0.00290989	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965352	CTAAGCTGTACAGTT[G/T]GAGGTCCAGCGAGTC	51317
rs757281216	snp	A/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084582	ATCACTACATACTGA[A/G]GATACAGAGCTGAGT	51317
rs757299379	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46048341	TCATTCTATATGTAG[C/T]ACTTCATTCCTTTTT	51317
rs757328685	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46023268	AGGCAGGCCGGGATC[C/T]GGCAGAGAGACAGCT	51317
rs757331516	in-del	-/TTTA			intron-variant	PHF21A	GRCh38.p7	11:46059895	CCACGCCCAGCTGAT[-/TTTA]TTTATTTATTTTTGG	51317
rs757343295	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45960117	CTGTGGAAAACAGTT[C/T]GGCAGTTCTTCAAAT	51317
rs757357943	in-del	-/AAAAAAAAAAA			intron-variant	PHF21A	GRCh38.p7	11:45968932	GCGAAACTCCATTGC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA	51317
rs757366978	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997699	AGACAAAAGCCAATC[C/T]ACCTGTTCAGGATCT	51317
rs757368931	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46012820	CTCATCTTAATGATA[C/T]CCTAAGAGCTCATGC	51317
rs757370110	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46063026	GATGACGGTTTCACA[C/T]CATCAAAAATTACTC	51317
rs757392692	snp	A/C/G	1.65343e-05	0.00287521	synonymous-codon, missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938295	GCAAACGCTGCAAAA[A/C/G]TCCTCATGAATATCA	51317
rs757404448	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46101784	GGGACTACAGGCACA[C/T]GCCACCACACTCGGC	51317
rs757419575	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45941904	TTCTCATAAAAATGA[C/T]GATAGTGGCAACACG	51317
rs757421257	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46048536	GCAATTTGGGAGGCC[A/G]AGGCAGGCAGGTCAC	51317
rs757457001	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46011539	TGAAGTAAGAAGATT[A/G]GCAATTTCTAAGATA	51317
rs757460674	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46046837	TTTCCAAACACTGAT[C/G]AAGGATTTCTCCCAT	51317
rs757509961	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46076958	CTGTCATGCATTACA[C/T]TGTGGCCATAATACC	51317
rs757521460	snp	C/T	2.48821e-05	0.0035271	intron-variant	PHF21A	GRCh38.p7	11:45965639	AGAATAATTATTGTA[C/T]TACTTAAGCTGCTCA	51317
rs757528655	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45938003	AGGGAATGAAGGCCA[A/T]GCGCCTGCGTGCTGT	51317
rs757558015	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45974655	AGACGTGATCTCGCT[A/G]TGTTGCCCAGGCTGG	51317
rs757559060	snp	C/G	1.66405e-05	0.00288443	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945875	GCAGGGACACAGGCT[C/G]AACAGGTGCAGGGAA	51317
rs757575641	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46027051	ACACGCACACATGCA[C/T]GCAAATCATCATTCC	51317
rs757575884	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46001848	GGATGGAGGTCTTTG[C/G]TTTCTATGACAACCC	51317
rs757588650	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46116309	TAACACATACAGATA[C/T]ACATCTTTTTCACTG	51317
rs757625314	in-del	-/TCA			intron-variant	PHF21A	GRCh38.p7	11:46117750	TGCTCAACATCCCAC[-/TCA]TCAACACAAGACTAA	51317
rs757651374	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:46021061	TTAGATAGATTCTTT[-/AA]AAAAAAAAAAAAAAG	51317
rs757665102	in-del	-/AGGAA			intron-variant	PHF21A	GRCh38.p7	11:46079856	GAAAGGAAAGAGGAA[-/AGGAA]AGGAAAGGAAAGGAA	51317
rs757677355	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46038864	TCACCTCTTAAAGGC[C/T]CCATCTTTCAGTGCT	51317
rs757688136	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45950045	GGAACATTAGACAGA[A/G]GGAAGGCAATTTTCC	51317
rs757690659	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46092139	TAACTATCCAGCTAG[C/T]ATCAGGATCAGGCAC	51317
rs757704513	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:46027014	CTTTTCTGAAAAATT[-/AA]AAGTCTGAGAGCAGG	51317
rs757704940	in-del	-/CTTT			intron-variant	PHF21A	GRCh38.p7	11:45945109	GACATTATATATTCA[-/CTTT]CTTATTATCTGCCTC	51317
rs757715634	in-del	-/GTG	0.000181821	0.00953297	cds-indel, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979805	AGCTGACTGCTGGGC[-/GTG]GTGGTGGTGGTACTG	51317
rs757722328	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46107268	GTCAAGATGACTGAG[A/T]CTAGAATAAAAAAGG	51317
rs757722963	snp	G/T	0.000185512	0.00962919	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935093	ACCCTCTTTCCCACT[G/T]GGACAGGCCGGGCTG	51317
rs757723103	snp	C/G	1.65954e-05	0.00288053	intron-variant	PHF21A	GRCh38.p7	11:45950160	ATTTTCAGGAACAAA[C/G]CTGTGGGCCAGAAAA	51317
rs757723511	snp	A/G	1.7586e-05	0.00296524	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965528	CATGACGGGCCTCTG[A/G]ATAAGCTGAGGAGCT	51317
rs757776350	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45948741	CTCATTCTCTTTTCT[C/T]TCCCATTCTCAGAGA	51317
rs757787438	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46083978	GAAAGGAAGTCAGGA[A/C]TACTTTAAGTTCTTA	51317
rs757810876	snp	C/T	3.71975e-05	0.00431247	intron-variant	PHF21A	GRCh38.p7	11:45935559	AGCCTGGGGCCCACA[C/T]GTACTGTTACGTATA	51317
rs757811418	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46054880	AGCTCTTTTAACCAG[G/T]AACGACTAGGACCAG	51317
rs757834075	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45987553	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	51317
rs757843526	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46005107	GCAGGCTCAGTTACC[A/G]AGAGCAACCGCAGTC	51317
rs757845246	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46068136	TGAGTTGCTAAAGGT[A/G]TCAGTGCTAATGAGC	51317
rs757882610	snp	A/G			intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935147	GTCTCTAGAAAGCCC[A/G]CTTCCTCACACTGGT	51317
rs757905835	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45949247	GTAAGCAGTGACTAA[C/T]AAAAATGATAAGTCA	51317
rs757920963	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46092347	ACACACACAAGTTTC[A/C]AAAGTTTTAAAACCC	51317
rs757926860	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46055162	AGCAATCTGAATGTA[A/G]AATCCTTCTGGACAT	51317
rs757931397	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46020636	ATGAAATTTCTCAAA[C/T]ATGAACATGACCCAG	51317
rs757931748	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46003593	GCAGAGTGAGAAAAC[A/G]CTACAATTCTCACTA	51317
rs757953113	snp	A/G	3.29511e-05	0.00405887	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979881	TGTAGTTTGTTTTCA[A/G]ATTGTGGCAATGGCT	51317
rs757957802	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46082186	ACACAAAGAACAAAA[A/C]TATGTTTTCACTCCA	51317
rs757992048	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45998336	TGTGAAAGGATGTTA[A/G]GGCCATGGATAGAGT	51317
rs757993851	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45965832	TTGATTCTAAACCCT[C/G]AGCTCCCTCTTCTAT	51317
rs758008933	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46107360	ATTAATTGAGCCCTC[G/T]GTACACTATTAGACT	51317
rs758013620	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46117637	CTACTCTATATCCTA[C/T]TTGTATTAATATTAT	51317
rs758033188	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46068927	TGCCCTATAATAATG[C/T]GGCACGTTATTAAAG	51317
rs758049202	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46033160	TATACCTGCAGTTCA[C/T]TCATTTTTTAAAAAC	51317
rs758098969	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46083820	CATATGGTAGTTGAG[A/T]TAGACATGTTGTTAT	51317
rs758113439	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46017093	CTCCTGCCTCAGCCT[C/T]CTGAGTTGCTGGGAT	51317
rs758138972	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46046476	AGAAACCAGAGCTCG[C/T]CATACAGGGCAAGAG	51317
rs758151377	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45988580	ATAGCACAGGCACAT[-/A]AATTTTAAAAGATTC	51317
rs758152527	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45986672	TCAGAAAAATATTGG[C/G]AATCAAATTAATTAA	51317
rs758173258	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46114675	TACTTATTTAAAATT[A/T]AAAAAAAACACACAC	51317
rs758180407	in-del	-/TGTCA			intron-variant	PHF21A	GRCh38.p7	11:45985319	GAGGGGATGTGTTAC[-/TGTCA]TAACATTAGAGACAA	51317
rs758211324	in-del	-/ATT			intron-variant	PHF21A	GRCh38.p7	11:45974422	GTCAAACGACAAATT[-/ATT]ATTATTATTATTATT	51317
rs758222202	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45979422	AGAGGTCAAGTCACA[A/G]ACTTTTAGAACAAGT	51317
rs758223283	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46031949	CACAGTTACCCAATT[C/T]TCCCCAATGCACATC	51317
rs758254725	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45957870	AAAGAATAACAAAAT[C/T]GACAAACCTCTGGCT	51317
rs758262888	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46098547	CTCTATAAAGTACAA[A/C]AATCCTTATTCACAA	51317
rs758290521	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929696	AGGGCCTTGTGGGAG[A/G]GGGCGCCAAGTGGAA	51317
rs758291150	snp	A/G	3.4239e-05	0.00413743	intron-variant	PHF21A	GRCh38.p7	11:45938125	GTCTTTGTCCTCCTC[A/G]GCCCCTCCCCTGTTG	51317
rs758308941	snp	A/G	7.12441e-05	0.005968	downstream-variant-500B, missense, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928838	CCCAGAGCCCTGCCC[A/G]AGGCTGAGGCTGGGC	51317
rs758309805	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46020382	CACCAAGAACCAGGA[A/G]CGCCTGCTCTGACAC	51317
rs758313325	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46044921	AAAAGATAGGAACTG[A/T]TCGAAGCTTTCAAAG	51317
rs758354504	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46097227	TCAAAATCCAAGACA[G/T]ATCTTGTTACTCCTC	51317
rs758378001	snp	C/T	1.6477e-05	0.00287024	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938251	ACACGGGAACATGTG[C/T]CGCACATCAGTAACT	51317
rs758394838	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46070859	ATAAGCATCAAATGC[A/G]TATCAATACATCTTC	51317
rs758404327	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093926	TACCATTTTAAAATA[C/T]AGTAAAAAGGAAAAG	51317
rs758426743	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45984993	AGAGGCTGATAGAGA[C/G]TTGTAACTTTTCACA	51317
rs758433365	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45968490	TTTCTCCACCCTGGA[A/G]CTACATACATGTTCT	51317
rs758498400	snp	C/T	3.50287e-05	0.00418487	intron-variant	PHF21A	GRCh38.p7	11:46076887	ATAGTAGCAGGAAGA[C/T]TATGCATACTGCATT	51317
rs758501208	snp	A/G	1.75194e-05	0.00295963	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934002	TGGTTACAGTTCGCT[A/G]TGCAGCTCTGGGAGG	51317
rs758505446	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46049977	AATCAAAGTAGGACC[A/G]TATTCTATCATATAT	51317
rs758514555	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45983551	ATGCCCTCTGTCACT[G/T]AAATATAGATGACTG	51317
rs758515015	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46013233	TGGCATAGGCACTGT[-/G]AATAGAAAATTCCAG	51317
rs758537875	snp	A/T			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46088586	GTGTGACTACTCTCA[A/T]CCCCAGGGTTCATTT	51317
rs758618164	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45944919	TTACAGGAGCACGCC[A/G]TGCCCGGCTAATTTT	51317
rs758618899	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46035047	ATGAGGACTGAAGAG[A/G]TTTGCTGCTTCTTGC	51317
rs758619255	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46077255	TTTTCTCCACTTGCC[C/T]TCTCCCTTATTTAGC	51317
rs758634582	in-del	-/CAGT			intron-variant	PHF21A	GRCh38.p7	11:45953346	GGACCCTCAAGACTA[-/CAGT]CTAAGAATTCCACTC	51317
rs758640476	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45959661	ATCCATAAAACAAAT[A/G]CTAGAGCTAATAAAC	51317
rs758653240	snp	A/G	1.64768e-05	0.00287021	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946027	CAAGAGAAGGGAACA[A/G]AAGGGAAAAACGGGG	51317
rs758671691	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46009701	AGCCAGAGCAGACTT[A/C]CAACTTGGGCAGTTT	51317
rs758673710	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46042595	TCTTATGACTAGGAC[A/C]TGGTGCTAGATCTGA	51317
rs758683143	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46064515	GGAGTAAATCAACTT[C/T]GGGAAACATATCTTC	51317
rs758708353	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45943538	GGTCTTCCTGCTTCC[A/G]TCCTATTTTCCCTAT	51317
rs758708504	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45961354	TTAGTCAAGGTTAAA[C/T]AGATTGGGATTGAAG	51317
rs758711545	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46011708	CTTTCAAGCAATGTA[C/T]TTAGCTAACAAAAGT	51317
rs758714241	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46102025	ACCACGCCCAGCTAA[C/T]TTTTGTATTTTTAGT	51317
rs758716021	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46067335	TGAGTTCAATGGGGA[A/G]GCGGGCATGAGTGAG	51317
rs758721117	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46013264	AAAAAATAATCCATA[A/G]GTTTTAAACTGCACG	51317
rs758744210	in-del	-/TGT			intron-variant	PHF21A	GRCh38.p7	11:45961639	TCTGAATTGACGACA[-/TGT]TGTTACATAGAAGTC	51317
rs758750469	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46116482	TAAAATCAACTACTA[A/T]CACATCACATCAATG	51317
rs758764795	in-del	-/AGAA			intron-variant	PHF21A	GRCh38.p7	11:46098507	ATAGCAGAAATAAAT[-/AGAA]AGAAGAAATCTTGCT	51317
rs758765300	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46040255	CATAATGGTCTCACC[C/T]CAGTGGAAAAGAGAG	51317
rs758773216	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46078576	AAAGAAAAGTTAACA[C/T]TCTCTGTTAATTTTT	51317
rs758826006	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45981516	AGCATATAATAACTA[C/T]TTGGGGCCATATTTG	51317
rs758845364	snp	A/G	2.63376e-05	0.00362879	intron-variant	PHF21A	GRCh38.p7	11:45969933	AAGATAAATAAACCA[A/G]AGAGAACAATTACTC	51317
rs758845514	snp	G/T	3.31148e-05	0.00406894	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945901	GGGAAAGTGAATGTG[G/T]TCTCTGTCTTTTCAT	51317
rs758855518	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46028811	ACTCCTGACCTCATC[A/G]TCCACTCGCCTCGGC	51317
rs758872460	in-del	-/TGATTTTA			intron-variant	PHF21A	GRCh38.p7	11:45940661	TCCTTCATTATTAAA[-/TGATTTTA]ATCAGGCTGAGGGCT	51317
rs758888131	snp	C/T	1.64819e-05	0.00287066	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935675	CACCTTTTGCTCTAG[C/T]TGTTCTCGTTCTTGT	51317
rs758923722	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46091623	AATTTCAAAGTCAAG[C/T]TTCCACAGTTAAATT	51317
rs758924849	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46007975	TCTTTTTCTGTCTGT[A/C]CTTGGGATTACCATG	51317
rs758943466	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45973536	CTTAAATGTGAAATG[A/C]GAGTAAACGCGGAAC	51317
rs758957915	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45978310	CGTCTCAAAAAAACA[A/G]TAACAAAAAAACAAA	51317
rs758998545	in-del	-/ATAAT			intron-variant	PHF21A	GRCh38.p7	11:46008708	AATAAAAGGAAAATA[-/ATAAT]ATATGTTTTACATAT	51317
rs759030034	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46040603	AATACAATCTAGTGC[A/C]CCAAAAATAACAGTA	51317
rs759043116	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46109778	TTGAGATCAGGAGTT[-/A]AGAGACCAGTCTACC	51317
rs759049610	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46069067	AAAGGAGAGCAGATA[A/G]TACAGCACTGGGAAC	51317
rs759050993	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46072890	TTAAGATTGCCTCTA[A/C]AAGAAAGCAAAATGA	51317
rs759087625	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45970629	CTGACACGGTTAATT[G/T]GTGAGTTTCTTGAAT	51317
rs759093524	in-del	-/AGC	1.69186e-05	0.00290844	intron-variant	PHF21A	GRCh38.p7	11:45971098	TGATCACACATGAGG[-/AGC]AGCAGCTGCTGGCTT	51317
rs759108775	in-del	-/AG			intron-variant	PHF21A	GRCh38.p7	11:46024902	ACCATAGTGACTCCT[-/AG]AGTTCTAGACTAGTC	51317
rs759114228	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46112069	TCTGAAGTCAACCAA[A/G]GGCTTGTGGTATGGA	51317
rs759120687	snp	C/T	1.64961e-05	0.00287189	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934126	CAGGTTTGGAGAGGT[C/T]GATGCCGTGGATGAG	51317
rs759122878	in-del	-/ACT			intron-variant	PHF21A	GRCh38.p7	11:46032496	TTTTTTCAATTCTCC[-/ACT]ATTATTTAAAAAAAC	51317
rs759126173	snp	A/T	0.000258904	0.0113748	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965339	AAGACTTGGCTTGCT[A/T]AGCTGTACAGTTTGA	51317
rs759165496	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46102144	TACAGGCGCGAGCCA[A/C]CACGCCTGTCCCTGT	51317
rs759178517	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46074461	GGCTCTTTTGGCGGG[-/A]AGGGGGGAAGGCATA	51317
rs759183848	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45944011	AGACTGAGAAACTCT[A/T]CCAAAATAAAGGATT	51317
rs759220764	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45946256	TGACAGAAGGTGCTG[A/G]CTTATGTAGAAAGAC	51317
rs759229225	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46088214	AACAAATCAGTTGCT[C/G]CAAAGTGAATACCAT	51317
rs759235526	snp	A/G	1.6543e-05	0.00287597	intron-variant, stop-gained, nc-transcript-variant	PHF21A	GRCh38.p7	11:46076822	TTAAGTCAGCATTCT[A/G]ATTGGAAAGAAAAAA	51317
rs759247970	snp	A/G	3.35745e-05	0.00409709	intron-variant, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946085	ACATACCTTTGGCCA[A/G]TGTTCCTCATTGGCT	51317
rs759250089	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46099659	CCTAGAAAACTCAGA[-/G]TAGGCCTTACCGAAG	51317
rs759310849	snp	C/T	1.662e-05	0.00288266	missense, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934051	TGGAGGTGGCGGCAT[C/T]GGCAGGGGGGGTGCA	51317
rs759316955	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46086394	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCG	51317
rs759318478	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45961029	TCAATTATTATCATG[C/T]TTGTCTTACTTATTA	51317
rs759323487	snp	A/G	1.69413e-05	0.00291039	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953613	CATCTGTTTCTGTGT[A/G]AGATTTAACTGTCTA	51317
rs759328442	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46101280	GACAAATGAAAATAT[C/T]ATCCTAAAAGGGATT	51317
rs759338087	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46035651	CTAATCTATAGGTCA[A/G]AGAAGGCCTCTAGGA	51317
rs759369474	snp	A/C/T			intron-variant	PHF21A	GRCh38.p7	11:46063989	AAATAAAATCACATA[A/C/T]TCAGAAAAACAAATT	51317
rs759410662	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46117227	AAGCAGATTTATCAA[A/G]CTTTCTAGCATCCCC	51317
rs759427728	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46049548	TAGAAGAGGGTGTGG[C/T]GGGGGAAGGAGGGAT	51317
rs759448601	snp	A/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118865	TCTTCAAAGACCAAA[A/T]GCAAAGCTGACCTAT	51317
rs759468297	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46029494	GGAGTTCAAGACCAG[C/T]CTGGGCAACATGGTG	51317
rs759481559	snp	A/G	2.04975e-05	0.0032013	intron-variant	PHF21A	GRCh38.p7	11:45969907	TTGCCTGAACCTGCT[A/G]AAAAATGAGGAAGAT	51317
rs759482092	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46112857	AAAGAGACCTGTATC[A/G]CCACATGCATAAAAA	51317
rs759521447	snp	C/T	3.29571e-05	0.00405924	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945985	AACCCCAGCACTGCA[C/T]TGTATTTTGGAGGAC	51317
rs759543941	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46039807	CTAGAGTCCTTGACT[A/G]AAGTCAGAGGAAATA	51317
rs759635538	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46054589	TGAGAACCAGCAGTT[C/T]ACACGTAGATGTGGC	51317
rs759639226	snp	A/T	1.64817e-05	0.00287064	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979812	TGCTGGGCGTGGTGG[A/T]GGTGGTACTGCTGCT	51317
rs759642350	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46076694	TCTCTTAGAAGCCTC[A/G]AGCAGACATATCTTT	51317
rs759660221	in-del	-/GA			intron-variant	PHF21A	GRCh38.p7	11:45996505	ATGATTTCCCTTTTT[-/GA]GAGACAGAGAGAGAG	51317
rs759687616	snp	A/G	0.000185546	0.00963009	intron-variant, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935241	TGGGCCCACTCGCTC[A/G]GGTGACTAGGAAGAA	51317
rs759696677	snp	A/G			synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965327	TACCTGTTTTTCAAG[A/G]CTTGGCTTGCTAAGC	51317
rs759711538	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932889	AGCCTGAAAAACAGC[-/T]TTTTCTATTCCTTAT	51317
rs759713354	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46100603	CCTTGCACTAAATGA[C/T]AGATGCCAAATAACA	51317
rs759723452	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46052705	CTACCAGTTTTTCAC[C/G]ATGTGCCCTGGTGGA	51317
rs759734384	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45966439	TCTACTTCTATCCTC[A/T]CTCCACTATCTACTA	51317
rs759738698	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46106549	AGTTACAAAGTTTGG[C/T]CTTCGAGATATGATG	51317
rs759770676	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45939264	ATAAATCTTACAGGT[-/A]ACGGAAATCCATTCA	51317
rs759770799	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46026705	GTGGGCTTTTAAATC[C/T]GTAATTAAAAAACCT	51317
rs759783379	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46068526	GAAGAGTCCCTAAAC[A/C]TTCTGAAATACAGAT	51317
rs759810309	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45940863	GGACTTGGGATAAAC[A/G]AAGAGGCGTTCACTT	51317
rs759822074	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46063016	TCTTGATCGTGATGA[C/T]GGTTTCACACCATCA	51317
rs759831740	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46081472	TAGAAGCTGAAAAAG[A/G]TTTTCTTCCAGACAC	51317
rs759860613	snp	A/G			downstream-variant-500B, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928973	AGCATCTGTGGGGTG[A/G]GGTCTTCCCCTTGCT	51317
rs759873830	snp	C/T	1.71223e-05	0.00292589	intron-variant	PHF21A	GRCh38.p7	11:45934251	TGACAAGGGCAGTGG[C/T]ACTGAGCCGCCTGGT	51317
rs759880723	in-del	-/AAAGAATGCAT			intron-variant	PHF21A	GRCh38.p7	11:45985997	TGTTTAACAGATGGC[-/AAAGAATGCAT]AAAGAATGCATATAT	51317
rs759890140	in-del	-/AAAAAA			intron-variant, cds-indel, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119745	GAACGTGGTCAGGGG[-/AAAAAA]AAAAAAAAGAAATCC	51317
rs759924939	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46016757	AGCCCACTACCTGGA[A/G]CTTGGCAGCCCTCAG	51317
rs759948570	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930483	CCCCAAAGGGCCTGA[C/T]AAGGAAGGAAGAAAT	51317
rs759950446	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45995601	TCCATTAACCTTCCA[C/T]ATGAGAGCTCCCCTG	51317
rs759991160	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45962139	AGTTCCGTGAGGGTA[C/T]GGGCTTTAGTTTATC	51317
rs760024902	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45939046	CACGTGTTAGCCAGG[A/T]TGGTCTCGATCTCCT	51317
rs760027684	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042752	TATAAAAGAGGCCTA[C/T]GAAAGCTTGTTTTTC	51317
rs760030594	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45964690	AGAGGTCTTTCTGCT[A/G]CAGAACCTTCAAGTA	51317
rs760038648	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45994062	AATGCTGGAGCCAAC[C/T]CAACAAGAATGATAT	51317
rs760049104	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46080190	TTGAGACAGGGTCTT[A/G]CTCTGTCACCTAGGC	51317
rs760084461	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46097554	CTAAAACTATAATCA[C/G]AATTGTTCCGCTCCC	51317
rs760087166	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46097828	TCTCCCTAACTAGAA[C/T]ACACACACACACATA	51317
rs760095965	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46009221	TCAGGTAATCTGCCC[A/G]CCTCGGTCTCCCAAA	51317
rs760113994	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46046281	GTGCCAATAGCACTG[A/G]GGCCATCCTCCTATG	51317
rs760127730	in-del	-/TT	7.01508e-05	0.00592203	intron-variant	PHF21A	GRCh38.p7	11:45935574	GTACTGTTACGTATA[-/TT]TTGGAAAGGCCTAGG	51317
rs760145728	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45954957	AGATCTTTGATTTTC[C/T]TTCCTGGCCACTTCC	51317
rs760147167	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46059837	ATTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCCA	51317
rs760172374	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46113756	GCTTGAACCTGGGAG[A/G]TGGAGGCTGCAGTGA	51317
rs760172996	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45972339	TTATATGGCCTAAAC[A/T]TCTATCTGGAGATAG	51317
rs760201937	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46044237	GCTGTCCTATAGTAC[A/T]GCTAGAGGTACCTTT	51317
rs760205715	snp	A/C	1.7098e-05	0.00292381	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965342	ACTTGGCTTGCTAAG[A/C]TGTACAGTTTGAGGT	51317
rs760216920	in-del	-/TCAG			intron-variant	PHF21A	GRCh38.p7	11:45966335	CCTCCGATAATTGCC[-/TCAG]TAAGTACCCTTTTCT	51317
rs760217972	snp	A/G			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46075087	ATGCAAACTTAGTTC[A/G]GAGAACAATTAGAGC	51317
rs760224018	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46095323	ATGCAAGTTTGATTT[C/T]TTCATGTTAAGCTGG	51317
rs760244246	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46014482	GAACATACAAGTGCA[A/T]GTGTACTTTTTGGTA	51317
rs760258324	snp	G/T	1.64844e-05	0.00287087	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938213	TTGTTTTCAGAGGGG[G/T]GTCTAAGCAGTCCAA	51317
rs760258671	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46046340	AAGGGAAACCCACTT[C/T]TGGAGGCAAAAAAAG	51317
rs760296152	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46060008	CTCGGCCTCCAAAGC[A/G]CTGGGATTACAGGCG	51317
rs760308964	in-del	-/ATAA	2.27234e-05	0.00337064	intron-variant	PHF21A	GRCh38.p7	11:45969921	TAAAAAATGAGGAAG[-/ATAA]ATAAACCAGAGAGAA	51317
rs760320447	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45977417	GTTGGGATTACAGGC[A/G]TGTGCCACTGTGCCT	51317
rs760331775	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45955203	TACTTCATGCAGAGC[A/G]GGTGTATAGTAAAGA	51317
rs760337436	snp	C/T	1.67075e-05	0.00289023	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084266	TATAGTTTCTTCAGC[C/T]TCTGTTTAAAGTAAC	51317
rs760372163	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46008222	TCCTAGACTAATCCA[C/T]AATGTTCAGATGATA	51317
rs760373236	snp	C/T	1.69427e-05	0.00291051	intron-variant	PHF21A	GRCh38.p7	11:45934239	TTCTGCAGCAAATGA[C/T]AAGGGCAGTGGCACT	51317
rs760379463	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46024183	TTCTTTCTCCTCCTT[-/C]CCATCACAACCTGAT	51317
rs760388967	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46025327	GTCCCTTTCACACAA[C/T]ATGACCAATAGGAAA	51317
rs760405638	snp	A/G	1.651e-05	0.0028731	intron-variant	PHF21A	GRCh38.p7	11:46079193	GAGAGAAAAAGAGCC[A/G]TCAGTCTTACATATT	51317
rs760425502	snp	A/G	3.31066e-05	0.00406844	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965455	GCCCATTGACGACAC[A/G]GACGGGGTGGATGGA	51317
rs760438510	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45984696	ACCAGTTTATTCCTA[C/T]CAAAAATTGCTCCCA	51317
rs760451046	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45934468	AGGGAGAAAGAGCAT[A/G]CGGGCACCAACACAC	51317
rs760454574	snp	C/T	8.74669e-05	0.00661255	intron-variant	PHF21A	GRCh38.p7	11:45938109	TCCTCCTGATGGCCG[C/T]GTCTTTGTCCTCCTC	51317
rs760480418	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45985923	TAAACAAATTGACAA[C/G]AGCAGCAACTGTAAT	51317
rs760485812	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46088361	TGCAATCTTCCAAAC[A/G]GTACATGTCAAACCA	51317
rs760489313	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46024096	AAAGCAAGGAAAGGG[A/C]AAGGTGGTGTCTGGG	51317
rs760510631	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46000911	GGCAACAAAAGTGAA[C/T]CTCCGTCTCAAAAAA	51317
rs760511958	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46050591	TGAAGTAGGTACTTC[C/T]ATAATTTTAATTCAT	51317
rs760600562	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45999457	TAGTATATACTTCCA[C/T]CAGGTTCTATTCTTT	51317
rs760646572	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46104996	GAGCAGAAAACTAAG[C/T]TTCAGTACCATTTAT	51317
rs760686806	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45944719	TTCACCACTCTTCAT[A/G]AACATCAGCCTCCTG	51317
rs760687723	snp	C/T	4.71698e-05	0.0048562	intron-variant	PHF21A	GRCh38.p7	11:45965632	GAAAGAGAGAATAAT[C/T]ATTGTATTACTTAAG	51317
rs760710794	in-del	-/AG			intron-variant	PHF21A	GRCh38.p7	11:46079872	AGGAAAGGAAAGGAA[-/AG]AGGAAAGGAAAGGAA	51317
rs760712574	snp	A/C/T			intron-variant	PHF21A	GRCh38.p7	11:45962471	CGAAGTAAGAGAATC[A/C/T]TGAGAATGCAATCTA	51317
rs760763836	in-del	-/TT			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084681	ACAACAGAATCATAA[-/TT]TTTTTTTTTTTTTTT	51317
rs760764047	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45983593	CAGTAACTGAAAGCC[-/A]GGTGAGCTCTGCAGC	51317
rs760784561	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46026633	TCTGAATTAGAAAAT[G/T]CAAAAAAAAAATCCT	51317
rs760786916	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46039904	GTTTAGCTTTCTGCA[A/T]CTTCCCAAGACTTCC	51317
rs760792263	in-del	-/CAA			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119561	CTCATCACAACAACT[-/CAA]CTACTTAGAAATCAC	51317
rs760821093	in-del	-/TAAA			intron-variant	PHF21A	GRCh38.p7	11:46108586	ATATATATATATATA[-/TAAA]ATACATATGTAAATG	51317
rs760832047	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45949927	TCAGAAGAGCACTTC[A/G]CTGTGCTGTTCAGAA	51317
rs760837849	snp	C/T	1.6569e-05	0.00287824	intron-variant	PHF21A	GRCh38.p7	11:45950285	AACAAAAGAAGAATA[C/T]GCTTCAGTCTGGGTT	51317
rs760843401	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46041520	CATCTTGGTTTCAAT[C/T]ATAGCCAGGCCAAAA	51317
rs760848268	snp	C/T	3.29679e-05	0.00405991	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935637	TGAGGTTTACTTACA[C/T]TTATGGAATTGCTGA	51317
rs760849805	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093317	TACTCCAATAGTGTC[C/T]CATTGCCTCAGGGAA	51317
rs760874583	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46023233	TTTAAGTGTAAGCAA[C/T]GGTTTCTTAGCCTTC	51317
rs760874852	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46054682	ATTCAAATCACTATA[C/G]TCTCACTAATATGCC	51317
rs760891034	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46056127	TAAAGTAACAAAATA[A/C]CCTTTATGTAATTTA	51317
rs760899712	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46020286	CAGAGTAAGATCCTA[C/T]GACATGTTTGGGGAC	51317
rs760904586	snp	C/T	0.000135079	0.00821713	intron-variant	PHF21A	GRCh38.p7	11:45935543	CAGAAGGACCCGAAA[C/T]AGCCTGGGGCCCACA	51317
rs760937352	snp	C/T	0.000144734	0.00850563	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933935	TGTTCTCCTTGCCGC[C/T]GGGATCCCGTGGCTT	51317
rs760939944	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46108005	TGTAGGGTATCTTTA[C/T]GCTGATTAAGCAGTA	51317
rs760987950	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46033813	GTAGGTGGCTGCTAG[A/G]AATCTTTTAATTACA	51317
rs761060978	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932502	CTAGAGACACACACA[C/T]GGCAAAATGTCATCG	51317
rs761073999	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46003343	TGTCTAGTCATCACT[C/T]AGACTCTCTTCGGTG	51317
rs761086135	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46034224	ATTAGTGCCCCCACC[C/T]CCCCCTTGCATACTT	51317
rs761086862	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45980572	GCTATTCACAGGTGT[A/G]GTCATAGTGCATGCA	51317
rs761090145	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46073209	GGCGGGCGCCTGTAG[A/T]CCCAGCTACTTGGGA	51317
rs761123409	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46068655	CTCAGCTAAGCAATA[G/T]ATGAGCAAAGTGGAA	51317
rs761140254	snp	C/T	1.64738e-05	0.00286995	intron-variant	PHF21A	GRCh38.p7	11:45979740	ATCTGCAGCCTGCAA[C/T]GTTCCATCCACACAT	51317
rs761161029	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45961783	GCCCCATTTTAGAGC[A/G]CTGGAGAGGACAAGG	51317
rs761176797	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45979220	AATGAAGTTTCACCA[C/T]GTTGGCCAGGCTGGT	51317
rs761192502	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45980817	AATATGCCATATAAA[C/G]AACACATTCTAAATT	51317
rs761213449	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46083486	CTTATCCTTCTCTCC[A/G]CTCCCATATCCCCAA	51317
rs761215126	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46067855	AAGTACCACAATGAG[C/T]GCCAAATAAAGTAGG	51317
rs761230321	snp	G/T	1.64817e-05	0.00287064	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946042	AAAGGGAAAAACGGG[G/T]AGGGAAAGAGAGGGG	51317
rs761234769	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46032715	CTATCTCTTACAAGT[A/G]CACAGACTTGATACC	51317
rs761239339	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46083728	GAAATTTAAACATCT[G/T]TGAAGATAATCACAT	51317
rs761242486	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46034228	GTGCCCCCACCCCCC[A/C]CTTGCATACTTTTCC	51317
rs761250900	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997090	AAAATTAATAAGACG[C/T]TTAGTATTTCTGAAA	51317
rs761275991	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45974136	AGCATCTACATACCT[C/G]TTTGTCTAGTATACA	51317
rs761279830	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46098996	AATTCAAATAAAAGT[C/T]ACTAAGAAAGGTCAA	51317
rs761303006	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46081662	AACTTTAAGCTGACA[C/T]TGTGTTAACAAAGTT	51317
rs761321132	snp	A/G	4.94425e-05	0.0049718	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938219	TCAGAGGGGGGTCTA[A/G]GCAGTCCAAATGATA	51317
rs761331454	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46099213	GTAAACCCAACTATA[C/G]CCAGAAGCTTATCCA	51317
rs761353711	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46062628	GCACATTAGCAGCTT[C/T]CCTTAAATATCTAGT	51317
rs761370712	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45998145	ATACAAACCATTCTA[C/G]TCGTCTTTGTTTTAA	51317
rs761400036	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46100711	TGAGATGGAATAATT[A/G]CACCTGTGGGTCTAA	51317
rs761402299	snp	G/T	1.64765e-05	0.00287019	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979866	TGCTGCTGTGCTGTT[G/T]GTAGTTTGTTTTCAG	51317
rs761419937	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46046333	AATATGCAAGGGAAA[C/T]CCACTTCTGGAGGCA	51317
rs761461080	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45997377	GGACTATACTTCTTA[A/C]AATCCAAATATAAAG	51317
rs761461626	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45941509	AATGGCAAATGATGG[C/T]TTAGTATCATTATGA	51317
rs761478416	snp	A/G	1.86034e-05	0.00304982	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965567	GGGAGGTGGTGCTGG[A/G]GCAATAGGAATGTTA	51317
rs761503250	in-del	-/TA			intron-variant	PHF21A	GRCh38.p7	11:46095958	TTCTCTTCCCCTTAC[-/TA]TATACCAAGCTGATA	51317
rs761517079	snp	G/T	1.65627e-05	0.00287769	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965461	TGACGACACGGACGG[G/T]GTGGATGGAATTCTG	51317
rs761521602	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45942704	TTCTATGACCCTAGT[C/T]CTCCAAAGGTAACAC	51317
rs761551573	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45979990	TGAAGACAAAAAGAA[A/T]TAAAAGATATTAGAA	51317
rs761565197	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45936038	CTCCTAGGACTTTGG[G/T]AGGCCAAGGCAGGTG	51317
rs761565724	snp	C/G	1.71091e-05	0.00292476	intron-variant	PHF21A	GRCh38.p7	11:45938343	GAAAGGTAAGAAAAA[C/G]GACAAAAAAGGTAAA	51317
rs761575760	in-del	-/G	1.66921e-05	0.00288891	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934055	GTGGCGGCATTGGCA[-/G]GGGGGGGTGCAGTCC	51317
rs761596730	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46061829	TTGGTTCACTTTCTC[A/G]TTTGATGGAGAACCT	51317
rs761606805	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46026660	TCCTTTAAAGTCAAG[C/T]AGTGGAATTAACATA	51317
rs761607908	snp	A/C	2.02427e-05	0.00318134	downstream-variant-500B, utr-variant-3-prime, synonymous-codon	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928867	GCCGGCGCTGCCCCT[A/C]ATCTTAGCATTGGGC	51317
rs761628740	in-del	-/A	1.64966e-05	0.00287194	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946058	GGGAAAGAGAGGGGG[-/A]AAAATGATCTTACAT	51317
rs761642226	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46009929	AAACAGATAAAGGGG[C/T]CGTCAGTCACTTTAC	51317
rs761651047	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45988351	GACAGAAAAAGACAA[C/T]AATATTAGAAAAATA	51317
rs761655188	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45937410	TATAAAATATCGACA[G/T]CACTTTACACTTAGT	51317
rs761657335	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45970951	AGTGATTTGAGCAGA[C/T]AGCAGAAATGCCATA	51317
rs761684507	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46075219	CAAATCTATGTTAGT[A/T]CTCACAAACAAAAAT	51317
rs761695242	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46106464	GGCATCTGTTCCTTT[C/G]AGAAAAAGAATTCTG	51317
rs761704449	snp	C/T	8.26754e-05	0.00642891	intron-variant	PHF21A	GRCh38.p7	11:46084132	TTAGCCATTACTTAA[C/T]AACAGTGTGGGAGAA	51317
rs761747345	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45986518	AAAGTATAAACACAT[A/C]AACTACAATCGAACA	51317
rs761749780	snp	A/G	1.69887e-05	0.00291446	intron-variant	PHF21A	GRCh38.p7	11:45934244	CAGCAAATGACAAGG[A/G]CAGTGGCACTGAGCC	51317
rs761772185	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45941580	ACTCCCAGACTACAC[-/T]TTTGAGAACTGCTGC	51317
rs761802655	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46052428	GAATTGAGTTTCTAT[C/T]ACTGGAAAGCAGAAG	51317
rs761803546	snp	A/G	1.64768e-05	0.00287021	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946018	CCTATATACCAAGAG[A/G]AGGGAACAAAAGGGA	51317
rs761826469	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46063182	TGAATTGAATTCGCC[-/G]GGGGGGGCTGGCATG	51317
rs761850741	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46094984	AACTGCTTCCTACTA[C/T]ATGCTAAATTCTATA	51317
rs761858007	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45989950	TGAGCCATGATCGTG[C/G]CACTGCACTTCAGCC	51317
rs761871600	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45948303	AATGTCCATGGGAAG[G/T]TCTGAAATATGGGAT	51317
rs761882381	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46079724	TGAGAACAAGGAAGT[A/G]CAGGAACAATACAAA	51317
rs761890443	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930389	GGCACACGATGGTGC[C/T]AGCTGGAGGCTGCCA	51317
rs761923398	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45961117	AAAGTGGAAAAATAA[A/G]TAAAAAGTCCAGTTG	51317
rs761930119	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46028745	CGCCCAGCTAATTTC[C/T]GTATTTTTAGTAGAG	51317
rs761954165	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46064026	TCTGTCGATTAACAC[C/G]CTCCCCCAATTTCAC	51317
rs761963993	snp	A/G	1.9297e-05	0.00310614	intron-variant	PHF21A	GRCh38.p7	11:45935748	TCTTTTGCTAAAAAA[A/G]AAAAAAAAAAAAAAA	51317
rs761967160	snp	G/T	4.77943e-05	0.00488824	intron-variant	PHF21A	GRCh38.p7	11:45965635	AGAGAGAATAATTAT[G/T]GTATTACTTAAGCTG	51317
rs761970057	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46078281	TACTTCCAAAAATCA[A/G]TGTGCCTCAGTACCA	51317
rs761992892	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46019452	TGAACCAGGTCCACA[C/T]AGCCCTAAGATGTGG	51317
rs762020114	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46041713	TTGTAAAATTTCAAA[C/T]ATACATAAAAGTTCA	51317
rs762053708	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45953099	GGTTGTAACAAAAAC[A/G]CACACTTAACAACTG	51317
rs762054471	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45945231	GCTCAGTGAGTATCT[C/G]CTGAGTGAATTCTGA	51317
rs762102676	snp	C/T			missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934213	GGATGGTGTTCTTCA[C/T]TTCCATGCATTTCTG	51317
rs762121112	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46003323	TCTTTTCACACCATC[-/T]TATGTGTCTAGTCAT	51317
rs762128276	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:45987069	TAATTATGAATGCGT[-/AA]AAGAGATGCCCAATT	51317
rs762160490	snp	C/G/T	3.29621e-05	0.00405958	synonymous-codon, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935654	TATGGAATTGCTGAG[C/G/T]TGTTTCACCTTTTGC	51317
rs762183820	snp	A/G	0.0001882	0.00969869	intron-variant, synonymous-codon	PHF21A	GRCh38.p7	11:46049400	GGCCCAAATACATAC[A/G]TTCAGTAGGTCAAGC	51317
rs762185994	snp	A/C	2.26411e-05	0.00336453	intron-variant	PHF21A	GRCh38.p7	11:45969918	TGCTAAAAAATGAGG[A/C]AGATAAATAAACCAG	51317
rs762188169	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46058196	GAAGGAGAAAGGTTA[A/C]ACTGCTAATATTCTT	51317
rs762201819	in-del	-/CCAAGGTAATGAAGC			intron-variant	PHF21A	GRCh38.p7	11:46069572	CTTACTTATTTGACT[-/CCAAGGTAATGAAGC]CTAAAGGCAATGTAA	51317
rs762221161	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45991312	GTAGCTAGTGAATTC[C/T]ATAACTGTTACATAA	51317
rs762240874	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45966645	TTGTTGTTTGAGATG[A/G]AGTCTCGCTCTGTTG	51317
rs762247145	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46022935	TTTGTATTTTTAGTA[C/G]AGATAGGGTTTCGCC	51317
rs762276758	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46004990	TCTCTTACTGCAAAT[A/G]TCTCTGAATATGGAA	51317
rs762307222	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45967660	TCATTGAAGACAAAT[A/G]TCTGATGCTATCTTG	51317
rs762311333	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46108175	AACCAAGAAGAGAGA[C/T]TACCAGTTTTTTTAA	51317
rs762320973	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45991331	ACTGTTACATAAAAA[C/T]GAAGTAATAATATCA	51317
rs762322912	snp	C/G/T	1.69246e-05	0.00290896	intron-variant	PHF21A	GRCh38.p7	11:45953512	TGAGACCTGCCTTTG[C/G/T]AAACATAGGCCTACC	51317
rs762337114	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45967836	TTTACTCTGTAATCA[G/T]CATGTGCCTATAGAC	51317
rs762354962	snp	C/T	1.66001e-05	0.00288094	intron-variant	PHF21A	GRCh38.p7	11:45950295	GAATATGCTTCAGTC[C/T]GGGTTCTCACAAAGC	51317
rs762368476	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46020335	AGTGGCTGCTAGTAT[C/G]CTGCAGCAAACCAAT	51317
rs762384328	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46069809	GTTAAATGTTAAATG[G/T]TCTAAGCTTCTTAGA	51317
rs762387866	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46069955	ACTCAATGGATACAC[A/G]TGCATTAACTCCTCA	51317
rs762448246	snp	C/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085228	TGGATATTTTAAAAT[C/G]TATCTATCGTGTGTA	51317
rs762449517	snp	C/T	1.80726e-05	0.00300599	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933950	CGGGATCCCGTGGCT[C/T]CTCCTAGAGGGGCTC	51317
rs762453351	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45952985	TCTATCCTAAATTAT[A/G]GTATAGATGTTACTA	51317
rs762463305	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46087788	TGAGATAGGGTCTTA[C/T]TGTGTCACCCAGGCT	51317
rs762490864	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PHF21A	GRCh38.p7	11:46120976	CCTGGCAGCTGGAGG[C/T]AGGAACTCTGAGCAG	51317
rs762525865	snp	A/T	3.32298e-05	0.004076	intron-variant	PHF21A	GRCh38.p7	11:45950300	TGCTTCAGTCTGGGT[A/T]CTCACAAAGCCAATT	51317
rs762530779	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45944163	TGTATATTTTATATA[C/G]TAATATTTTATTAGT	51317
rs762544183	in-del	-/ACACAC/ACACACAC			intron-variant	PHF21A	GRCh38.p7	11:46099527	AGAAAAATTAGACAC[-/ACACAC/ACACACAC]ACACACACACACACA	51317
rs762553284	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46086090	AAGGGAGACATACTA[C/T]GGTGAACAAATCTGG	51317
rs762556129	snp	C/T	1.64912e-05	0.00287147	intron-variant	PHF21A	GRCh38.p7	11:46076747	CCCCCCTCCCCTTTT[C/T]CCCTACCTGTTTCTC	51317
rs762603086	in-del	-/ATAGTCATATA			intron-variant	PHF21A	GRCh38.p7	11:46069513	TATTAGAGGCTGGAG[-/ATAGTCATATA]TCAGGTAACCAACAC	51317
rs762609466	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45937527	CTCTTGTCACCCAGG[C/T]TGGAGTGCAGTGGTG	51317
rs762643829	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46101092	TGGTGGTCCATACAA[C/G]CATCACAGACAGGAA	51317
rs762644355	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46034465	TCTGGTCTTCTTATC[A/G]TACTAAGGAAGGTCT	51317
rs762655532	snp	A/G			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46121685	GGAGGGGGCCGCCGG[A/G]CGGAGTGGTACGGCG	51317
rs762696470	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45998164	TCTTTGTTTTAAAGA[C/T]TGGTAACTTACTCAC	51317
rs762700198	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46010986	TTCTCTCTCTCTCTC[A/T]CACACACACACCCCT	51317
rs762727884	snp	A/C	1.83118e-05	0.00302582	intron-variant	PHF21A	GRCh38.p7	11:45945794	GATAACGCTTTTCCC[A/C]ATTTAAGCTCTCAGA	51317
rs762728766	in-del	-/CAC			intron-variant	PHF21A	GRCh38.p7	11:46040920	ACACACACACACACA[-/CAC]ACACACACACACGCA	51317
rs762732241	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46047877	CCATTATTAGGCTGG[C/T]ATTCTTATTGAAAAT	51317
rs762733912	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46099711	TTATTCCAAATCCAC[A/C]TTTCAAGCACTAAAA	51317
rs762741203	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46115929	AGTTAATAACACCCT[G/T]AGAGGTTTCATTTTT	51317
rs762747971	snp	A/G	0.000122527	0.00782613	intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46049493	TAGAGGGAAACAGAT[A/G]GCTTCTAAAAGGGGA	51317
rs762752070	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46063675	CCACTTTACCCATAA[A/G]GTATATAATTAAGCA	51317
rs762765033	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46012242	TGTCTTTCCTGACCT[C/T]TTTGTGCAGCTGCAC	51317
rs762782673	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45997487	CAAAAGATGAAGCCA[A/G]CCCATGCCTACGTGA	51317
rs762788309	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46026802	GACATTCTGTCCCAC[A/G]TGACTCACCCACTCA	51317
rs762803344	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46116789	CCAACATGGTGATAC[A/C]CCGTCTCTACTCAAA	51317
rs762811035	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45990865	AACATTTGTTACAAT[C/T]GAACCTACACTGACA	51317
rs762834030	snp	A/G	1.67781e-05	0.00289634	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965489	CTGGGATGTGGGAAG[A/G]GTTGTGGGGGTGAAC	51317
rs762843623	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093201	AATTAAAACTTTTCC[C/T]TTAATATTTTAGTAT	51317
rs762847019	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46062719	CTCATACACTACTGA[A/G]AGGAATGTAAAATAG	51317
rs762849538	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46027602	TGAAGCAAGCCAATC[A/G]ACGAAATGCACTGCT	51317
rs762864694	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46093789	CCTATTAGGGCTTTC[-/A]ATGTTAGCTCTTTTA	51317
rs762882144	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:45997427	CTTGCTGCACGTTAC[-/AT]ACTAGAGGATTCAGC	51317
rs762886500	in-del	-/T	4.04973e-05	0.00449967	downstream-variant-500B, utr-variant-3-prime, frameshift-variant	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928869	CGGCGCTGCCCCTCA[-/T]CTTAGCATTGGGCAG	51317
rs762887659	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45973079	GTGAGACTTCGTCTC[A/C]AAAAAAAATAAATAA	51317
rs762897439	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45976289	CTCCTTGACAAGTAC[C/T]TTCTGATCCCTCTAG	51317
rs762968259	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46007274	AAGCCAGGAATCTGT[A/G]GCACTTTACAGAAGA	51317
rs763028589	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46067018	GCACCTCATTATTTT[G/T]TAACAGCTACATGTT	51317
rs763048650	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46113671	TCTCTACTAAAAATA[A/C]AAAAATTAGTTGGGC	51317
rs763075716	snp	A/G/T	3.36272e-05	0.00410032	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965363	AGTTTGAGGTCCAGC[A/G/T]AGTCTGGTCCCTGGA	51317
rs763078523	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932984	GAACAAAAACAAAAA[-/T]TAAAGAAAGAGAAAA	51317
rs763090637	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45934358	TGCAGCCCCTGGGCC[G/T]TGCTGTGTTCCTCAG	51317
rs763095635	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45977808	TTGGTTTTATACAGT[A/C]TTGGTATTGCTTTTT	51317
rs763101503	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45965189	ATTATCGCACATAAG[C/T]GACAGCTTACTGACA	51317
rs763105823	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45996854	CCCTAACCACAGTAA[C/T]CTAAAAAAGGTCAAT	51317
rs763117576	snp	C/T	1.64822e-05	0.00287068	intron-variant	PHF21A	GRCh38.p7	11:45948997	TAGTGTGGTTATTAC[C/T]AATACTGGCACAAGC	51317
rs763128360	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46079898	AAGGAAAAGAAAGGA[A/G]AGGAAAGGAAGAAAA	51317
rs763131008	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46016649	CACATGACATAATCT[A/G]TTTTACACTGCAATT	51317
rs763132806	snp	A/G	1.73887e-05	0.00294857	intron-variant	PHF21A	GRCh38.p7	11:45971395	GAAAACAGATATTAG[A/G]ACACTAAATCTAAAC	51317
rs763190181	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46081158	TAATCAAAAGTCTTT[C/G]TCCCTGATGCTAAGA	51317
rs763191232	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45962537	CCTCTAAGACTATTA[G/T]GCCAGGCTGCCCAGC	51317
rs763199074	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45938964	TCAGCCTCCAGAGTA[G/T]CTGGGACCACAGGCA	51317
rs763227003	snp	A/G	1.64754e-05	0.00287009	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971201	TGGAGGTTGACTGGT[A/G]TGTTCTGCACATCAG	51317
rs763251091	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46102851	GTTTTGATAATAGCT[C/T]AGTATCTCCCTGTTT	51317
rs763277279	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46074632	CTCAGCCTCCCAAGT[-/A]GCTGGGACTACTGGC	51317
rs763315176	snp	G/T	1.65633e-05	0.00287774	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953587	GATGGTGCGGCTCTC[G/T]GTTTGTTTCTCATCT	51317
rs763340232	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46043894	TGGATGTGAGTGCAG[A/C]AAACAGTAAAAGATG	51317
rs763360904	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46007486	GTCCAGCTTATTTTT[C/G]TATTTTTAGTAGAGA	51317
rs763390612	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45951448	TTTATATTATTTCTT[A/C]TTTCAAAAACTGAGA	51317
rs763407053	snp	A/T	2.3747e-05	0.00344572	intron-variant	PHF21A	GRCh38.p7	11:45935764	AAAAAAAAAAAAAAA[A/T]GGAACGGTTTTTGAC	51317
rs763417460	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46100030	CTTTGAAATGTCAAT[A/G]AGAAGTGGAAACAGC	51317
rs763422411	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46002799	GTTTTATCTTTATTC[A/C]AAAGACCCTTCTTCC	51317
rs763427142	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45992995	CAGAAAACTGAAAAC[C/T]ACCTTGCTGAAGCTA	51317
rs763432411	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042596	CTTATGACTAGGACA[C/T]GGTGCTAGATCTGAA	51317
rs763442151	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46006333	AAATTCTTAATCTTT[C/T]GGTTGTATATACAAT	51317
rs763447365	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45953411	GAATAATAAAAGTGC[A/G]TAAGAAAATGAACAT	51317
rs763448478	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46023857	GCTACTCAGGAGGCT[A/G]AGGCAGGAAAATTGC	51317
rs763461381	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45967078	TTATGATAAAAATGA[-/C]CCTTTCCTGGCCGGG	51317
rs763487639	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46111813	TAAAGAATTAAGATT[C/T]TTTGAAACTACACTT	51317
rs763514252	in-del	-/TG			intron-variant	PHF21A	GRCh38.p7	11:45979354	CTTTCTATCTGGTCC[-/TG]CAAGAGCACTGATCC	51317
rs763539107	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45968868	CCTGGTGGGTGGAGA[C/T]TGCAGTGAGCCTAGA	51317
rs763548993	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46018948	ATCAATGTATCATAC[C/T]GTAAGCAGCAAGAAC	51317
rs763565588	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46016199	ACCATCATATATGTG[A/G]TCTGTTGTTGACCTA	51317
rs763580840	snp	C/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933745	AACCTCCAGCTGGCA[C/G]TATTTCATGTAACAT	51317
rs763600694	in-del	-/AACATGACAAAACCCCGTCTCTACT			intron-variant	PHF21A	GRCh38.p7	11:45968743	GAGACATTCCTGACC[-/AACATGACAAAACCCCGTCTCTACT]AAAAATACAAAAATT	51317
rs763603680	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46110290	AACTTCCCAAGAGTG[C/T]ACAGCTACGTGACAG	51317
rs763614385	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45994328	TTTATCTTACTGCCA[C/T]AAAAATTATGTAGCT	51317
rs763621548	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46038735	AAGCATGCTAGCATA[C/G]TTGCTCAGGTTTCTC	51317
rs763638669	snp	C/T	1.72276e-05	0.00293487	downstream-variant-500B, stop-gained, synonymous-codon, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928825	GCCCTGCAGCAGCCC[C/T]AGAGCCCTGCCCGAG	51317
rs763643908	snp	C/T	1.64743e-05	0.00287	intron-variant	PHF21A	GRCh38.p7	11:45979743	TGCAGCCTGCAATGT[C/T]CCATCCACACATTTA	51317
rs763648897	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45941461	CAATATCTGGTAAAC[C/G]CCACTGTTCGGTCTT	51317
rs763659808	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46031765	GAAAAGAATGCAATA[A/C]TTTTTTTCCAGAGAC	51317
rs763681087	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46044368	GGGTCAGCTGACCTA[C/T]TCAAATCTATAGTGA	51317
rs763688711	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005068	CTAATACAGCAGTCC[C/T]CCACATCAGTAATTT	51317
rs763697760	snp	A/G			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122225	TGAAGGGGGGGGGGG[A/G]AAGCCGTGAGGGGCA	51317
rs763702708	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45957130	AACAGAGCCCCAAAA[C/T]ATATGAAGAAACTAT	51317
rs763725156	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46097854	ACATACACAAAAGAA[C/T]AGAATACCTTGTACA	51317
rs763756378	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46060282	AGATTACAGGCATAA[A/G]CCACTACACCCCAAC	51317
rs763761687	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46073199	CAGGCGTGGTGGCGG[C/G]CGCCTGTAGTCCCAG	51317
rs763782838	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46035877	AAATTTGCGAGCCAC[A/G]TTAAGATTTTGGACT	51317
rs763789737	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46117650	TATTTGTATTAATAT[C/T]ATAGGGATGATAACA	51317
rs763804794	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45953088	TGTAATACAATGGTT[G/T]TAACAAAAACGCACA	51317
rs763853870	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46090157	TTGAAAATGGAGGAG[A/G]TTGGGGAGTAAGGTA	51317
rs763907329	snp	A/G	1.64876e-05	0.00287116	synonymous-codon, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934133	GGAGAGGTCGATGCC[A/G]TGGATGAGGCGAATC	51317
rs763985455	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46001072	AGTAATGCTACAGCA[A/C]TAGCTCAACATATCT	51317
rs763989266	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45984933	CTTTTATTCCTTCCA[A/T]GAATCAACATGCAAT	51317
rs763991894	snp	A/G	0.000237913	0.0109041	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965348	CTTGCTAAGCTGTAC[A/G]GTTTGAGGTCCAGCG	51317
rs764003224	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45973036	TGAGCCGAGATCACA[A/C]CATTGCACTCCAGCC	51317
rs764009363	in-del	-/AAAG			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45932986	ACAAAAACAAAAATT[-/AAAG]AAAGAGAAAAGAAAC	51317
rs764015682	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45959949	AAAAGATGCTCAGCA[C/T]CATTAGTCATTAGGG	51317
rs764047102	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46037334	TCTTCTAGCCTTCAG[A/G]CCTATTGATAAAAAA	51317
rs764048353	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46062976	GAGACGACCAAGAAC[A/G]CTTCAGAGGTGATGC	51317
rs764094089	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46088394	CTGATATCTAATGGC[C/T]TCTAACTTTCCAATA	51317
rs764099034	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46039851	CCTAAGATTAAAAAT[A/G]TCTGCATGAATGAAA	51317
rs764101290	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46048074	AGTTGCACAACTCCA[C/G]AATTAATTCCAGAAC	51317
rs764105516	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45974515	CTAGAGTGCAGTGGC[A/G]TAATCACAGCTCACT	51317
rs764120309	snp	C/G/T	6.49039e-05	0.00569635	intron-variant	PHF21A	GRCh38.p7	11:45969914	AACCTGCTAAAAAAT[C/G/T]AGGAAGATAAATAAA	51317
rs764162797	in-del	-/ATTATA			intron-variant	PHF21A	GRCh38.p7	11:46014004	ATTTCTTTGAAAAAC[-/ATTATA]ATTATATTTATTTAT	51317
rs764170278	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46035870	ATCACACAAATTTGC[A/G]AGCCACGTTAAGATT	51317
rs764177573	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46041612	AAGGTACAGGTCCTA[C/T]CCAATTTGTTGCTTT	51317
rs764201763	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46078109	TCCAATTTAAATTGT[A/G]ACTATACCAAAAAAA	51317
rs764212038	in-del	-/TATGAGT			intron-variant	PHF21A	GRCh38.p7	11:45941060	CCCAGAGAGCTTTTA[-/TATGAGT]TATATCTATTAATAT	51317
rs764225815	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46117236	TATCAAACTTTCTAG[A/C]ATCCCCAAATTTTTA	51317
rs764251737	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46026972	GCTTTTGCTAGCATT[C/G]TCCATTTTTATGTAG	51317
rs764277205	snp	A/G	1.68227e-05	0.00290018	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945859	GTGGAGGTGGGGCTG[A/G]GCAGGGACACAGGCT	51317
rs764285885	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45999575	TGAGAAGGGAAATTT[A/G]AAAATATATCTATAG	51317
rs764302743	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093320	TCCAATAGTGTCTCA[C/T]TGCCTCAGGGAATAT	51317
rs764328123	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930738	GCCCAGTGGGCAGCC[A/G]CTCCAGCTCTCTGAA	51317
rs764345327	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45949871	TGTAACTGTTGTCAA[C/T]ATTCTGATAACCTGG	51317
rs764364203	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45962617	AGAACATTGGCCAGG[C/T]GTGGTGGCTCATGCC	51317
rs764380998	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45991183	TAATAAGCATGTAAG[C/G]TTCTTCTATGTTTTT	51317
rs764390461	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46108006	GTAGGGTATCTTTAC[A/G]CTGATTAAGCAGTAC	51317
rs764394973	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46092034	CTACGTGAAATTAGA[C/T]AATTCATTTCCACTT	51317
rs764398471	snp	A/G	1.90911e-05	0.00308953	intron-variant	PHF21A	GRCh38.p7	11:45935550	ACCCGAAACAGCCTG[A/G]GGCCCACACGTACTG	51317
rs764400309	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45948588	CTTTTACATGGGGTT[C/T]TGTTCACTGTGCTAT	51317
rs764420297	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46040315	GGAAGGAAATACCTG[C/T]ACTACAGTGATGACA	51317
rs764433616	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46069514	ATTAGAGGCTGGAGA[C/T]AGTCATATATCAGGT	51317
rs764460167	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46067450	GGCCCCAGACTCATT[C/T]ACTAGTTTATACAAC	51317
rs764468772	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46004823	CCTCCTGAAAATACC[A/G]TCTCTCCCTCTCTCC	51317
rs764469990	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46018926	ATGCAAGACTTTTTA[G/T]GACAAAATCAATGTA	51317
rs764478304	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45966580	AACCTGAGGTAACAT[A/G]CCTGATTTTTAATAG	51317
rs764486568	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46107025	CTGTCCCCACGGCTG[C/T]CTCTTCTGCAGGAAG	51317
rs764508240	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46054690	CACTATACTCTCACT[A/C]ATATGCCACTAGAAG	51317
rs764567003	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46003468	AATATTCATAGTACT[A/G]ATGACACTAAAACAA	51317
rs764582150	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45982549	AATTAAACTGCTGTA[A/G]TTTAGGAGAAGGCAA	51317
rs764584691	snp	G/T	4.94442e-05	0.00497188	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979863	GGTTGCTGCTGTGCT[G/T]TTTGTAGTTTGTTTT	51317
rs764600709	snp	C/T	1.64803e-05	0.00287052	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979868	CTGCTGTGCTGTTTG[C/T]AGTTTGTTTTCAGAT	51317
rs764601160	snp	A/G	4.94173e-05	0.00497053	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45948914	CCCAGGGTGCATTGT[A/G]CTGTTTAGGTATGTC	51317
rs764633290	snp	G/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085364	AGATAATGTCAAAAG[G/T]CTAAATCTGTTAATA	51317
rs764636534	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46068666	AATAGATGAGCAAAG[C/T]GGAAAAAAAAAATAC	51317
rs764663741	in-del	-/A			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932678	TTAAGTAACACTAGG[-/A]AGACCTCAATATCTT	51317
rs764686399	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:46026063	TGCCAAGTTATCTAA[-/AT]ATATCCTGGTATCAG	51317
rs764726611	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46067860	CCACAATGAGCGCCA[A/G]ATAAAGTAGGCACAA	51317
rs764730185	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45979320	TACTGAGCCCAGCCA[C/T]AGCACCCTTCCAAAT	51317
rs764736732	in-del	-/TAAACTAAATAA	1.77491e-05	0.00297896	intron-variant	PHF21A	GRCh38.p7	11:45971406	TTAGGACACTAAATC[-/TAAACTAAATAA]TAAACTAAATCCCAC	51317
rs764739930	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45966652	TTGAGATGGAGTCTC[A/G]CTCTGTTGCCAGGCT	51317
rs764755191	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45982337	GCCAATTTTGGGGGG[-/A]AAAATTCTGCTATGC	51317
rs764766209	snp	G/T	1.65869e-05	0.00287979	intron-variant	PHF21A	GRCh38.p7	11:45950162	TTTCAGGAACAAAGC[G/T]GTGGGCCAGAAAAAA	51317
rs764769862	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45979362	TCTGGTCCCAAGAGC[A/T]CTGATCCTGGAATAG	51317
rs764771772	snp	A/G	1.64738e-05	0.00286995	intron-variant	PHF21A	GRCh38.p7	11:45938352	GAAAAAGGACAAAAA[A/G]GGTAAAATTTTAATG	51317
rs764798357	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46081983	CATTCCATATGGAGT[A/G]AATACCCTGAAAATT	51317
rs764827710	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45980883	CTGGGACAGGTTCTG[C/T]GGCGGTACACACGTT	51317
rs764827793	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45992477	CCCAGGAGGCAGAGC[C/T]TGCAGTGAGCTGAGA	51317
rs764839102	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45944096	TGAAGCAGGAAAAAC[-/A]AAAGTGTCACAAAAG	51317
rs764839850	snp	C/T	0.000186237	0.009648	intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46049436	CTAGCTTCAACACAG[C/T]GTATTCCTGTACAGT	51317
rs764849967	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45942731	ACACTTTCTTTGTTA[C/T]CTCTGGAATTTTAAC	51317
rs764859496	snp	C/G	1.80873e-05	0.00300721	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933938	TCTCCTTGCCGCCGG[C/G]ATCCCGTGGCTTCTC	51317
rs764872886	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46099306	AGTCCTTGCTTTAAA[A/C]ACAGAAGAAAACTCC	51317
rs764881991	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45957595	GAGAGAAATGAAAAC[A/G]AGGCCACAACATACC	51317
rs764882805	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46047671	TGTTCTGACAAGAAG[C/G]CAGTGACTAACAACC	51317
rs764913000	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46061834	TCACTTTCTCGTTTG[A/T]TGGAGAACCTCCTCC	51317
rs764913623	snp	C/T	2.03668e-05	0.00319108	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928869	CGGCGCTGCCCCTCA[C/T]CTTAGCATTGGGCAG	51317
rs764983188	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46067256	AGACAGGTAAAAACA[A/T]CCCAGGTTGAAGAAA	51317
rs765013089	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45937500	GTATTATTTTTTTGA[A/G]ACAGAGTCTCGCTCT	51317
rs765013220	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46056365	GTTTCTATGACAAAG[A/G]TAACTCCAATTATGT	51317
rs765029626	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46052263	TGCCAGAGGCAACCT[C/T]TGCCAGTACAGGACA	51317
rs765043116	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45996332	TTATAGAGTGATCTA[C/T]ATTACAATTAGATCA	51317
rs765044358	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46083928	TTGTTAACACCTTTG[A/G]TATATGAAAAAAATC	51317
rs765045570	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45973002	GGAATCACTTGAACC[C/T]GTGAGGCAGAGGCTG	51317
rs765072599	in-del	-/TTGT			intron-variant	PHF21A	GRCh38.p7	11:46087673	GGTACATGTTGAATC[-/TTGT]TTGTTTAATTTTATT	51317
rs765110191	snp	C/T	4.94319e-05	0.00497127	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938239	TCCAAATGATATACA[C/T]GGGAACATGTGTCGC	51317
rs765112356	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45955579	AGTGCTTTTAAGGAA[A/G]GGCAAATCAATTCCT	51317
rs765125032	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46009974	ATAAGTATCCTAATT[G/T]GTTCAGCTTCTAACA	51317
rs765125860	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45987946	CTGTAGCTGCTGTGG[-/T]TTTTCCTCACAAAAG	51317
rs765139800	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45971013	ATGCTAGAAGAATGA[C/T]GGAAACTGAGAAATC	51317
rs765174841	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45944880	CCAGGGATTCTCCTG[C/T]CTCAGCCTCCAGAGT	51317
rs765181642	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120743	CCCCTCCCCTCCCCC[C/T]ACCTCCCCCCACAAC	51317
rs765184268	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46075303	TAAGTTATCTTAACT[G/T]TGCAACAGCATCCCC	51317
rs765229590	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45986644	AGCACTAAACTATAC[C/T]GCCCTCCTTCCTTCA	51317
rs765236363	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46014255	CACTTATAAATGAGA[A/G]CATATAATATTCAGT	51317
rs765245779	in-del	-/AAAAAAAAA			intron-variant	PHF21A	GRCh38.p7	11:45968934	GAAACTCCATTGCAA[-/AAAAAAAAA]AAAAAAAAAAAAAAA	51317
rs765259319	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46038459	TAACTATTTATTGAG[A/C]ACCTCCATGTGCTAC	51317
rs765272011	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46091735	ATCTTTTTTTAAGAG[A/G]TGAGGGTCTCGTTTT	51317
rs765304227	snp	A/C/T	4.94379e-05	0.00497161	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946025	ACCAAGAGAAGGGAA[A/C/T]AAAAGGGAAAAACGG	51317
rs765307583	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932897	AAAACAGCTTTTCTA[-/T]TCCTTATTTTAGTTT	51317
rs765312569	in-del	-/TC			intron-variant	PHF21A	GRCh38.p7	11:45996828	ATAGCAGTTTGTGTT[-/TC]TGAGTATATCCCTAA	51317
rs765324306	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46029793	AAATAACAAATGTCC[A/G]TTAGAGTGCTTTTAG	51317
rs765347957	snp	A/G	9.88517e-05	0.00702966	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971194	AGACGTCTGGAGGTT[A/G]ACTGGTGTGTTCTGC	51317
rs765356087	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46103315	TAAAGTAAAGAAAAC[G/T]TAATACTATATATTT	51317
rs765382988	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46064501	GCTTCCTAAACTTGG[G/T]AGTAAATCAACTTTG	51317
rs765406803	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45933273	GACTGGGCAGGCTTC[A/G]GGAGTGGTGGGGTTA	51317
rs765407101	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46042507	AAATCCTAGAAAACC[A/G]AAGAAAGAGATTGGT	51317
rs765413910	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45959304	TATATGTATATCAAA[C/T]CATCATGTTGTATAC	51317
rs765471348	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46078415	GATAAACACTCTCCA[G/T]ACTTATGACCTAGTA	51317
rs765502139	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45992573	TTTTTTGACATCACA[A/T]GGTGAACCAAAAATG	51317
rs765530893	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46025449	CCTTCCATGATAATC[A/G]ATTAGGTTAGCAGAG	51317
rs765535623	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45991378	CAGGTAGAACAATGA[C/G]GCTCTGAGTAATTAA	51317
rs765554527	snp	A/G	2.37285e-05	0.00344437	intron-variant	PHF21A	GRCh38.p7	11:45969925	AAATGAGGAAGATAA[A/G]TAAACCAGAGAGAAC	51317
rs765559540	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46077082	TTGAGCATCTTGTAC[A/G]GTAAGAGTACCTGTC	51317
rs765564076	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45992710	AAGTTATATGAATGA[A/G]TTCTGAGAATATGCT	51317
rs765593703	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46042521	CGAAGAAAGAGATTG[C/G]TGAAATGTATAGCAT	51317
rs765603829	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46042386	TAGTATGTGTGATAG[-/T]GCAACTCCGGAAAGT	51317
rs765613294	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46094798	TCAGCTACTCGGGAG[C/G]CTGTGACAGGAGAAT	51317
rs765620164	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005040	ATTTTAACACATGCA[C/T]GTATACACCCAACTA	51317
rs765628940	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45951357	TCAGCCTATTTGAAA[A/C]TAAACTTCTTCAGCA	51317
rs765644243	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46006198	AATGATTTTAAAATT[A/C]AATGTTATAAACTTC	51317
rs765646721	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45967666	AAGACAAATGTCTGA[A/T]GCTATCTTGCTCACA	51317
rs765653256	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093446	TTCATGCAGTTAGCA[C/T]TCATTTCCAAAGAAA	51317
rs765655766	in-del	-/CCTGCAG			intron-variant	PHF21A	GRCh38.p7	11:46058102	AGGATCTCACTTAAA[-/CCTGCAG]AAAACAGAAACTAGA	51317
rs765697829	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46069841	AAGTAGTACTTTACA[C/G]GTAAGATGAAAGTGT	51317
rs765699221	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46109697	TCAAGAATTTGTCTA[C/T]TGGGCCAGGCGTGGT	51317
rs765709203	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45957595	GAGAGAAATGAAAAC[-/A]AGGCCACAACATACC	51317
rs765718880	snp	A/G	9.24531e-05	0.00679838	intron-variant	PHF21A	GRCh38.p7	11:45935560	GCCTGGGGCCCACAC[A/G]TACTGTTACGTATAT	51317
rs765720602	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45950106	AATCATACTCTATTT[C/G]TGTTCCAATTTTCTA	51317
rs765744826	snp	C/T	3.32817e-05	0.00407919	intron-variant	PHF21A	GRCh38.p7	11:45950301	GCTTCAGTCTGGGTT[C/T]TCACAAAGCCAATTG	51317
rs765760692	snp	G/T	1.66164e-05	0.00288235	intron-variant	PHF21A	GRCh38.p7	11:45950297	ATATGCTTCAGTCTG[G/T]GTTCTCACAAAGCCA	51317
rs765768321	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46056904	CAAGCACAAACAGTG[C/G]GCTGAGGTACTTTTT	51317
rs765769421	in-del	-/AAG			intron-variant	PHF21A	GRCh38.p7	11:46101528	TTTTTAAATTTCCAT[-/AAG]AAGAAGTTATTTAAA	51317
rs765775594	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46071814	CAATTATGCTAATAT[A/T]TAAAGCTGTTAAAAA	51317
rs765784597	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46040429	CTTAGCAATCTAATT[A/G]TAAGTAGAAGAGAAA	51317
rs765834713	snp	C/T	3.29652e-05	0.00405974	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935682	TGCTCTAGTTGTTCT[C/T]GTTCTTGTTTTAAAT	51317
rs765851369	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45943562	TCCCTATAGGCCCTT[C/T]TCTTCTGCATATTTT	51317
rs765856510	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45951460	CTTATTTCAAAAACT[C/G]AGATGGGCACCTATC	51317
rs765856907	in-del	-/GCACCTATG	1.67147e-05	0.00289086	intron-variant	PHF21A	GRCh38.p7	11:45935594	AAGGCCTAGGTCTCT[-/GCACCTATG]GCACCTATGTATCGA	51317
rs765874631	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46005110	GGCTCAGTTACCAAG[A/G]GCAACCGCAGTCCAA	51317
rs765887601	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46057177	ACTGGGTCATGTCCA[A/G]TGGGCTAGTAATGCT	51317
rs765896594	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46047326	TGGAGTTGAAAACAT[C/G]AAAGAAAGGGAAAAA	51317
rs765902113	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45937593	TCAAGCGATTCTCCT[G/T]CCTCAGCTTCCCAAG	51317
rs765913676	snp	A/G	1.66665e-05	0.00288669	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934043	GGCCGGCGTGGAGGT[A/G]GCGGCATTGGCAGGG	51317
rs765925340	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45969049	ATATCATCTTATCTC[A/C]TATTAGCACTGCCCA	51317
rs765929008	snp	C/T	1.64876e-05	0.00287116	intron-variant	PHF21A	GRCh38.p7	11:46076750	CCCTCCCCTTTTCCC[C/T]TACCTGTTTCTCACT	51317
rs765935005	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46064017	ATTTCAAGTTCTGTC[A/G]ATTAACACCCTCCCC	51317
rs765942584	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:45969921	TAAAAAATGAGGAAG[-/AT]AAATAAACCAGAGAG	51317
rs765942961	snp	C/T	6.63801e-05	0.0057607	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953593	GCGGCTCTCTGTTTG[C/T]TTCTCATCTGTTTCT	51317
rs765975725	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46069992	AATCCAAACATTCCA[C/T]GAATATGGAAAGAGA	51317
rs765985715	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46034618	AGCAGACAAAAATTA[C/T]GGTGACTATCCAGCT	51317
rs766006304	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46035578	GATAAAATATAATGA[A/G]TGTTAGGATAAAGGG	51317
rs766008277	snp	A/C	0.000100338	0.00708229	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965486	ATTCTGGGATGTGGG[A/C]AGGGTTGTGGGGGTG	51317
rs766011459	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45998178	ATTGGTAACTTACTC[A/C]CAGCTAGGTTTCCAT	51317
rs766018076	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45967911	TGTGCTATGTACTCT[C/T]AATAGTTCATATTCT	51317
rs766035359	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46109714	GGCCAGGCGTGGTGG[-/T]TTTAGGCCTGTAATC	51317
rs766080929	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45977608	ACCCAATTCTGTTTA[A/C]AACTTAAACAAAAAT	51317
rs766104389	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46012410	TTGTTTCCTCCCTAT[A/C]GTCATTCCCTGGATA	51317
rs766109708	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45943050	TGATGGCTCTTCAAA[A/G]TATATGCAGACGTGA	51317
rs766116013	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46083940	TTGGTATATGAAAAA[A/T]ATCTTTTCAGTTCTT	51317
rs766124618	snp	C/T	0.000189807	0.00974	intron-variant	PHF21A	GRCh38.p7	11:46049533	AAACAGAAGGTCAGG[C/T]AGAAGAGGGTGTGGC	51317
rs766143791	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45965668	CAAGTCCTATAAAAG[A/C]AAATCTTCCACACTC	51317
rs766173265	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46081414	TCTTGATTTTCCTTT[C/T]TGATTTGGTTACCAG	51317
rs766174517	in-del	-/ATC			intron-variant	PHF21A	GRCh38.p7	11:45943098	TGCTTCTTCCAAGCT[-/ATC]ATCATCATCATCTTT	51317
rs766191435	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46048601	ATGGTGAAACCCCAT[C/G]TCTACTAAAAATACA	51317
rs766199078	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45981050	ATGTAAGCCCCATGA[A/G]TGCAGGGGCTTATTT	51317
rs766199908	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45941678	GCAGAGGAAGTCCTA[C/T]GGAGGCACCATACCA	51317
rs766199955	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45959653	CTCAAAGAATCCATA[A/G]AACAAATACTAGAGC	51317
rs766209867	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46116599	TGAGAAACTGACTAG[A/G]CAGCATTTTTTCAAA	51317
rs766265509	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46113899	AGATGTATTTTATAA[A/G]TAATTTTTCTTGAAG	51317
rs766278292	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930962	ACAGGGAGATTGGGT[A/G]CCAGGGGCCTCTTCT	51317
rs766286175	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45957871	AAGAATAACAAAATC[A/G]ACAAACCTCTGGCTT	51317
rs766288066	snp	C/G	2.25813e-05	0.00336008	intron-variant	PHF21A	GRCh38.p7	11:45965623	CCTATAGGGGAAAGA[C/G]AGAATAATTATTGTA	51317
rs766303940	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46011280	GATCACCTGAGGTCA[A/G]GAGTTCAAGGCCAAT	51317
rs766328194	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46115973	AGTGTTTTTCTCACC[A/G]TTCACAGAAGCAAGT	51317
rs766351823	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46037471	ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA	51317
rs766362418	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46062755	TCACTTTGGAAAACA[G/T]TTTGGCAGTTTCTTA	51317
rs766371382	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46076428	ACACGCAGCACCTAC[A/G]AGATTCTCTATCACC	51317
rs766378508	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46001498	CCAGTTGGTGTCTCC[A/G]TCACATGCACCACAG	51317
rs766382508	in-del	-/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932628	ATAGCACTTTTGTAA[-/T]TTTTTTTTACAATGT	51317
rs766404375	in-del	-/TG			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085189	ACAATGCAATATAAC[-/TG]TACTATCCACGAACT	51317
rs766409131	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45965242	TTGAGAAAATGTATT[C/T]AGAGAAAGCCCAGCA	51317
rs766424492	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45992177	CACCAGTTTTCAACC[A/C]TCAGACGGTAATTAC	51317
rs766431157	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46052437	TTCTATCACTGGAAA[A/G]CAGAAGAGTCTTCAC	51317
rs766479863	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997388	CTTAAAATCCAAATA[C/T]AAAGGACATCATTTT	51317
rs766480818	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46026649	CAAAAAAAAAATCCT[G/T]TAAAGTCAAGCAGTG	51317
rs766514920	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45948402	GATGCCCTCTTCTCA[A/G]AGATTCTAAGTTCTC	51317
rs766579906	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45999809	TGGGTGAGAAATTCA[C/T]CATGTTTCATTTTGT	51317
rs766580378	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46106547	CAAGTTACAAAGTTT[A/G]GTCTTCGAGATATGA	51317
rs766586238	snp	A/G	1.70313e-05	0.00291811	intron-variant	PHF21A	GRCh38.p7	11:45934246	GCAAATGACAAGGGC[A/G]GTGGCACTGAGCCGC	51317
rs766589406	in-del	-/CAAC			intron-variant	PHF21A	GRCh38.p7	11:46011930	CACAAAAATTAGAAG[-/CAAC]CTGCACACTCTAGGT	51317
rs766594839	in-del	-/AAATAA			intron-variant	PHF21A	GRCh38.p7	11:45989684	AATAAATAAATAAAT[-/AAATAA]AAATAAAAATAAAAA	51317
rs766604906	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45946825	GTCTGCATTTTATGA[C/G]GGTGGAGACCGGCAA	51317
rs766621759	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46065622	GCATCTGTACTGATA[A/C]AATTATAACATCTAT	51317
rs766640637	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46093290	TTAAATATGGTGTTT[A/G]TTGACTGATATTACT	51317
rs766673384	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45976302	ACTTTCTGATCCCTC[C/T]AGTCAAAATTACTCT	51317
rs766677590	in-del	-/TACTT			intron-variant	PHF21A	GRCh38.p7	11:46042031	GCAATTTTCCTACTA[-/TACTT]AATATGATTTGAGAT	51317
rs766693780	snp	G/T	1.64749e-05	0.00287005	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971208	TGACTGGTGTGTTCT[G/T]CACATCAGTGCTGAG	51317
rs766696087	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45977809	TGGTTTTATACAGTA[C/T]TGGTATTGCTTTTTT	51317
rs766711485	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46064539	TATCTTCTGAAAACA[A/T]AATTTTGCAGGACAG	51317
rs766716655	snp	C/T	2.84669e-05	0.00377262	intron-variant	PHF21A	GRCh38.p7	11:45969940	ATAAACCAGAGAGAA[C/T]AATTACTCTTCAATA	51317
rs766722499	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46078866	GCTATATGACAAGTA[C/T]TAACTCAATATTTTT	51317
rs766755880	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46031376	AAATGTAGCTCAGAT[C/T]GATTATGTCACTTCC	51317
rs766761246	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45993028	TAGGGAATTACAGTA[A/G]GCAAAATGTAATAAT	51317
rs766762001	in-del	-/AAAATACA			intron-variant	PHF21A	GRCh38.p7	11:46116802	ACCCCGTCTCTACTC[-/AAAATACA]AAACTTAGCCGGGCG	51317
rs766789598	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45953439	CATCGAGTTCATTTC[A/G]TCATTCAGAGAGCAG	51317
rs766819387	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46058343	ACATTGTTGGTAAAA[A/C]GAAACCTGATTAAGA	51317
rs766833436	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46096935	GTCATTCCCATCTCA[A/G]TAAATGGTAACTCCA	51317
rs766833550	in-del	-/ACTCTT			intron-variant	PHF21A	GRCh38.p7	11:46055389	AAACAAACACAACTC[-/ACTCTT]GATAACTGTTCTACA	51317
rs766845048	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46029959	AAGACATAATTTGGA[C/T]AGTCTTTATAACTTG	51317
rs766884228	snp	A/G	4.6476e-05	0.00482035	intron-variant	PHF21A	GRCh38.p7	11:45935765	AAAAAAAAAAAAAAA[A/G]GAACGGTTTTTGACA	51317
rs766884924	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45956732	AGAAAAAAATCAAAC[-/A]AAAAAAGGCAGTATT	51317
rs766892366	in-del	-/CACACACACG			intron-variant	PHF21A	GRCh38.p7	11:46040926	ACACACACACACACA[-/CACACACACG]CACGCACAATTAAGG	51317
rs766934156	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46006346	TTCGGTTGTATATAC[A/G]ATTAGGGCAAAGGCT	51317
rs766947449	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45951363	TATTTGAAAATAAAC[-/T]TCTTCAGCAAGCCAC	51317
rs766951685	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46039415	AAAAAGTCCAAGTCT[C/T]TGTCCCAGGCATAGT	51317
rs766978393	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45958195	AACATTTAAAGAATT[A/G]GCACCAATCTGTCTC	51317
rs767033768	snp	A/G			intron-variant, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935243	GGCCCACTCGCTCAG[A/G]TGACTAGGAAGAATC	51317
rs767080250	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45954960	TCTTTGATTTTCTTT[C/T]CTGGCCACTTCCATA	51317
rs767096979	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46112286	AACAGCCTGAGCTTC[C/T]GATCAAATTATATTG	51317
rs767099715	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46058427	TGACTAAAAAGGGCA[A/G]GCAGGAACTTAGTCT	51317
rs767128014	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46022860	AGATCTTGGCTCACT[A/G]CAACCTCCACCTCCT	51317
rs767133317	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46094987	TGCTTCCTACTATAT[A/G]CTAAATTCTATACAT	51317
rs767150306	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45984645	ACAGAGAAGGGAGAC[A/G]GAGAGACGGAAGGAC	51317
rs767164480	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45974678	CAGGCTGGTCTAGAA[C/T]TCGCTCTCACGTAAT	51317
rs767170100	snp	A/T			synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953608	TTTCTCATCTGTTTC[A/T]GTGTGAGATTTAACT	51317
rs767189862	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46072026	AAATATTATACTAAA[C/T]ATTATACTAGGAATA	51317
rs767197410	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46088243	ATCAGACTCACAAGA[C/T]AGTAACACACTGCAT	51317
rs767200214	in-del	-/G	1.66921e-05	0.00288891	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934056	GTGGCGGCATTGGCA[-/G]GGGGGGTGCAGTCCG	51317
rs767238404	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45999400	TGGTTGATTATAGGT[C/T]TCTAAACAGATAAAC	51317
rs767258078	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45969275	TGCTGGAAGAACACT[A/C]TCAGGAGAGTATGGT	51317
rs767262543	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46100614	TGATAGATGCCAAAT[-/A]AACATCATAACATTA	51317
rs767267964	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46110554	ATTCCTACAAACCTG[A/G]TATTTTCTATATTGG	51317
rs767276410	snp	A/G	5.74399e-05	0.00535879	intron-variant	PHF21A	GRCh38.p7	11:45953629	AGATTTAACTGTCTA[A/G]GAGAGAAAAATTAAA	51317
rs767280918	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997056	AGAGATATAAAACTA[C/T]CACAAAATCTTGGTT	51317
rs767330804	snp	A/G	1.64942e-05	0.00287173	synonymous-codon, stop-gained, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934127	AGGTTTGGAGAGGTC[A/G]ATGCCGTGGATGAGG	51317
rs767343267	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45944524	AAAGCCACAAAGCCC[C/T]GCGCAACTGGCCCAG	51317
rs767344740	snp	C/T	1.64773e-05	0.00287026	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945990	CAGCACTGCATTGTA[C/T]TTTGGAGGACGACCT	51317
rs767351697	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45968033	ACTAAACCTTAGATT[C/T]CTTACCCTAAAAAGA	51317
rs767357481	in-del	-/TA			intron-variant	PHF21A	GRCh38.p7	11:46108571	GTGTGTGTGTGTATA[-/TA]TATATATATATATAT	51317
rs767366464	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45981119	GGCCCAACACGGTGG[C/T]TCATGCCTGTAATCC	51317
rs767395445	snp	C/T	1.65504e-05	0.00287662	intron-variant, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:46076825	AGTCAGCATTCTGAT[C/T]GGAAAGAAAAAATAT	51317
rs767399971	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46027309	AAACAATATTCCATG[C/T]TAATCTGCCATCGTT	51317
rs767424652	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45939128	TGAGCCACTGCACCC[A/G]GCCGGGACTACTGTA	51317
rs767433042	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45943283	GCACACCAGTATGCC[C/T]GGCTAATTTTTGTAT	51317
rs767435299	snp	C/T	1.80237e-05	0.00300192	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933966	CTCCTAGAGGGGCTC[C/T]GTTATTTAGTCTCTT	51317
rs767444383	in-del	-/TAAC			intron-variant	PHF21A	GRCh38.p7	11:46096148	GCCCCAACATCTTAA[-/TAAC]CATCCCTCTTGTACC	51317
rs767505296	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46049641	ACTCTCCTTGCTGGT[A/T]GCCAGCATGCTCCCT	51317
rs767507866	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46101697	GAGTGCAGTGGCATG[A/G]CACAATCACAGCCTC	51317
rs767517523	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933604	CTCCTCCCTCCGCCC[A/G]TCCCTGCTCCCCACC	51317
rs767537060	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45949890	CTGATAACCTGGAGT[A/G]ACCAGAAAATATAAA	51317
rs767547750	in-del	-/AAG			intron-variant	PHF21A	GRCh38.p7	11:46069038	ACACAATCACACTCC[-/AAG]AAGACAGGTAAAAAG	51317
rs767570920	snp	C/T	1.95781e-05	0.00312868	intron-variant	PHF21A	GRCh38.p7	11:45935538	ATAAACAGAAGGACC[C/T]GAAACAGCCTGGGGC	51317
rs767578057	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46025788	ATTTGCAAGTCATAG[A/G]CATAATATGGCTTTT	51317
rs767582159	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46039842	TTAAATTTCCCTAAG[A/G]TTAAAAATATCTGCA	51317
rs767583902	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930506	GAAGAAATCAAAACC[C/T]CAGAGGAGCTCAGCA	51317
rs767594928	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46048216	TCTGTCTCCAGGGAG[A/G]TGCATATTCTAAACA	51317
rs767614926	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46055701	GGAGTCATGGAATCT[C/T]TTTATATAAACGCCC	51317
rs767621246	snp	A/T	1.69527e-05	0.00291137	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965500	GAAGGGTTGTGGGGG[A/T]GAACTTGGTCAGCAT	51317
rs767649073	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46106921	CCTTCAGCCTTTCAC[A/C]GAAAGAAAGGCTGTT	51317
rs767668078	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46038526	AGTTGTGTGATTATC[C/T]TTATTAGTTTACTGT	51317
rs767683177	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46075421	CTTGTCAAACTAACC[C/G]TGAAACTATAAGGAG	51317
rs767700629	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45967490	ATCCATTGTGGGGAC[C/T]TTGAAGCCATGCCTA	51317
rs767726989	snp	A/C	6.59098e-05	0.00574026	intron-variant	PHF21A	GRCh38.p7	11:45979723	CAACAAATCAGTCTA[A/C]AATCTGCAGCCTGCA	51317
rs767732910	in-del	-/AAAT			intron-variant	PHF21A	GRCh38.p7	11:46111476	GCAAGACTCCGTCTC[-/AAAT]AAATAAATAAATAAA	51317
rs767746637	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45987199	TTCAGTGAGCTATAA[C/T]CATGCCACTACACTC	51317
rs767753642	snp	A/G			upstream-variant-2KB	PHF21A	GRCh38.p7	11:46122721	AAGAATTCTTGTTTT[A/G]AGAGATTTCTTGGCG	51317
rs767771311	snp	A/T	1.64765e-05	0.00287019	intron-variant	PHF21A	GRCh38.p7	11:45949504	GAAGAAAAGGTTTTC[A/T]TTAGCAGAGAGGCAT	51317
rs767771602	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45948514	GACAACCAAGACGCT[A/G]TTAGGAACACCTTGG	51317
rs767772530	snp	A/G			downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929116	TTGTGTTCCTGGTTT[A/G]GGGGAGCAAGGGCAC	51317
rs767795717	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46090675	TAATACTTATTTTTT[C/G]TGGAAGTAGAATTCC	51317
rs767803038	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46039235	TTATCTCCTGTTTTC[A/G]TGCATTCGCTGTTTT	51317
rs767830337	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46065733	TACTCCTTTTCTTTA[A/C]CAAAAGTTGTTTAAG	51317
rs767842970	snp	C/G	1.71717e-05	0.00293011	intron-variant	PHF21A	GRCh38.p7	11:45934253	ACAAGGGCAGTGGCA[C/G]TGAGCCGCCTGGTTT	51317
rs767862784	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930632	TTACCAGGATGCAGC[A/G]CCTGGACAGGAGCTG	51317
rs767864248	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46031727	TTTCCTCTGGCTTTG[C/T]CTGTTAGGTCTAATA	51317
rs767909297	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45939054	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTGGC	51317
rs767912449	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46001633	TTTCCCCCATGCTTA[C/G]ATTTTTAAAATTCCA	51317
rs767912518	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46018792	GTACCAAGAATAACT[A/G]TAGGTAGGAGCAGAT	51317
rs767947366	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45957476	TAGAAATTAATGACA[A/G]CAGAAAAACTAGAAA	51317
rs767950141	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46043999	ACAAACTGAGGAAAG[C/G]TTAAGATTGTGGTTA	51317
rs767950387	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46106208	ATTCTACATTTGTAT[A/C]TGATTTGCTTTTTAT	51317
rs767989452	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45995897	TCATAATATTCAAAC[C/T]CCAAATTCATTATTA	51317
rs767989689	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45978030	TGGTGGGCCGGTTGC[A/G]GTGGCTCACACCTGT	51317
rs768002546	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46016762	ACTACCTGGAGCTTG[A/G]CAGCCCTCAGAAATG	51317
rs768003506	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45959076	TATGACAAAGCCAGA[C/T]TTATCCCAAGAGTGG	51317
rs768025889	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46099121	GAAGAAATTAGTGAA[C/T]TGCTAGAGAAAAATA	51317
rs768034063	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46062517	AGCATCCTCTCCTTG[A/T]TTCACTAATGCAATA	51317
rs768043819	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:46115690	TATGAAAATTCAAAC[-/AT]GTTTCAAGAAATCAG	51317
rs768053596	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46081571	TTCTATCTGTAAGCA[A/G]TTAAACTGCATTTCA	51317
rs768072903	snp	C/T	1.73075e-05	0.00294167	intron-variant	PHF21A	GRCh38.p7	11:45969796	AACCTATCATTGAGC[C/T]TGTCATTGGTTTACT	51317
rs768077632	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45994064	TGCTGGAGCCAACCC[A/G]ACAAGAATGATATAC	51317
rs768093817	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46040750	ATGTTCGAATTTAAA[C/T]ACCACTGCAATTTTT	51317
rs768111285	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46030125	CGCTAAACAATAGAG[A/C]AAACTGCTGACTCTA	51317
rs768123504	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45937753	CCCAAAGTGCTGAGA[C/T]TACAGGCCTGAGTCA	51317
rs768123939	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46076110	TTGCCACACTCCACC[C/T]GGTGGCAGGCACTGC	51317
rs768133654	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45988556	TAATTTAAAAAATCA[C/T]CTACAGTAATAGCAC	51317
rs768143527	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46080220	CTGGAGTACAGTGGT[A/G]TGATCATGGCTCACT	51317
rs768150140	in-del	-/AAAAA			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123378	AAATTCTGATTTCTT[-/AAAAA]ATAAAATATGGACTT	51317
rs768177079	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45956820	TAAGTCCCTCCTTAC[C/T]AGTAATCACTTAAAT	51317
rs768180934	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:45937354	CCAAAGAGAGAACGA[-/G]GGAGGCTAGGACAGT	51317
rs768183687	in-del	-/TAAA			intron-variant	PHF21A	GRCh38.p7	11:46075854	TTGTTATTATTTCAC[-/TAAA]TAACATTAAGTAACA	51317
rs768192823	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46116505	CATCAATGGAGAAAT[A/G]AAGAAAAACTGTAAT	51317
rs768219765	in-del	-/AGA			intron-variant	PHF21A	GRCh38.p7	11:46051828	GGTGGGGAAACATGC[-/AGA]AGAAGAAAAGATAAA	51317
rs768255059	in-del	-/TA			intron-variant	PHF21A	GRCh38.p7	11:46064451	GCTAGGATGAGAGAG[-/TA]GTTAGCCAAACCCTG	51317
rs768265110	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46063085	AATTATGACTCAATA[A/T]ACCTATAAGAGAGAA	51317
rs768290622	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46027328	TCTGCCATCGTTTAC[C/T]TTATTTATACATGTA	51317
rs768292837	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46010896	CAGGCAGTGAACAGC[A/C]TCATACCAGCTCCTT	51317
rs768302997	snp	A/G	3.38444e-05	0.00411352	intron-variant	PHF21A	GRCh38.p7	11:45938333	AAGTTGAGAGGAAAG[A/G]TAAGAAAAAGGACAA	51317
rs768343161	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46072382	CTTGCTCTTTGTTGC[G/T]TCTCCCCCTTCTTAC	51317
rs768344315	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45972554	AAACCGAGGCAGGTG[C/G]ATCGTCTGAGGTCAG	51317
rs768346889	snp	A/G	0.000185649	0.00963277	intron-variant, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935208	TGTGGAAGAAAGAGC[A/G]AGGGAGGGCCGTACG	51317
rs768357642	in-del	-/ACAC			intron-variant	PHF21A	GRCh38.p7	11:45955284	GTCTTTCTCTCTCCA[-/ACAC]ACACACACACACACA	51317
rs768374914	snp	A/G			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46075095	TTAGTTCAGAGAACA[A/G]TTAGAGCTTGCCACT	51317
rs768375908	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45988339	GTTTTCTTAGAAGAC[A/C]GAAAAAGACAATAAT	51317
rs768376481	in-del	-/TC			intron-variant	PHF21A	GRCh38.p7	11:46038117	GTATACTCCTATTTC[-/TC]TCTCTCTCTCTTTTT	51317
rs768379386	snp	G/T	1.67116e-05	0.0028906	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084267	ATAGTTTCTTCAGCC[G/T]CTGTTTAAAGTAACA	51317
rs768385457	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45948186	GTACCTTGTTTATGA[G/T]CTCAAACCCTGAGCT	51317
rs768388903	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46018347	ATGATCTGTTAGCTG[C/T]GCATCATGAAGGTCT	51317
rs768399577	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46039297	TACTCAGCTTCATTC[C/G]CCACTTTCAATCTGC	51317
rs768416356	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46052352	CCATGCCTGAAAGCA[C/G]CTATATCCCTGAACT	51317
rs768443735	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46092456	AGTTTTTCAAGACAA[A/G]CAAAAGTAAGTAGTT	51317
rs768451272	snp	A/C/T			intron-variant	PHF21A	GRCh38.p7	11:46014260	ATAAATGAGAACATA[A/C/T]AATATTCAGTTTTCT	51317
rs768456465	snp	A/C/T	3.29664e-05	0.00405984	intron-variant	PHF21A	GRCh38.p7	11:45949519	ATTAGCAGAGAGGCA[A/C/T]GGAGAACCTAAAAAA	51317
rs768491253	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46054038	TTCACAAGCAACGTC[A/G]TGGCAGTGGAGGAAG	51317
rs768493678	in-del	-/AAAATAAAAT			intron-variant	PHF21A	GRCh38.p7	11:45975323	TGTCTCAAAGAAAAC[-/AAAATAAAAT]AAAATAAAATAAAAT	51317
rs768501327	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46098050	ACTGCCTGCCTTACA[A/G]TACTCTATTTCCTTC	51317
rs768539399	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46107527	ACTGCTACATTCTAC[C/T]AGGTCCAATTCTTAG	51317
rs768553398	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46086631	TTCTTCTTGAAAACA[A/C]CACTTGGTTTTAATT	51317
rs768580628	in-del	-/CTG	4.22003e-05	0.0045933	downstream-variant-500B, cds-indel	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928914	TGCCCTCCGCCATCC[-/CTG]CTATTTAAATTATTT	51317
rs768588384	in-del	-/TGA			intron-variant	PHF21A	GRCh38.p7	11:46100123	ATGCCTCAATCACGC[-/TGA]TAAGTAAGTAGTCCT	51317
rs768598732	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46094793	TAATCTCAGCTACTC[A/G]GGAGGCTGTGACAGG	51317
rs768607195	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46066769	TATAAAGTTAAACGT[G/T]CTAGCTCTCTTGAAC	51317
rs768631999	in-del	-/A	0.000137377	0.00828671	intron-variant	PHF21A	GRCh38.p7	11:45938346	GGTAAGAAAAAGGAC[-/A]AAAAAAGGTAAAATT	51317
rs768646418	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46044474	CCCCATTTGGATTTC[A/T]TATCTTATTTTCCAA	51317
rs768687273	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46096338	CTAGTTATTGTCCCC[A/G]TCTAGGCTCACGTTT	51317
rs768687714	in-del	-/ATATAA			intron-variant	PHF21A	GRCh38.p7	11:46108583	TATATATATATATAT[-/ATATAA]AATACATATGTAAAT	51317
rs768688582	snp	C/T	1.64822e-05	0.00287068	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979792	TGGGAGAGGCTGCAG[C/T]TGACTGCTGGGCGTG	51317
rs768692641	snp	A/G	1.64732e-05	0.0028699	intron-variant	PHF21A	GRCh38.p7	11:45948966	GAGGGTTGAAGGAGG[A/G]AAGGTGACTGTTGAG	51317
rs768693677	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016448	TTTCCTGCCTCTGTA[C/T]CTTTGCCTTTGCTTA	51317
rs768708847	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45965041	GAGGGCAGCAGAGCC[C/T]GTCTGTGAATTTCCA	51317
rs768746508	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119178	TATCCATTATTTATA[C/T]ATAAATGTTCTTCCC	51317
rs768773068	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45953069	TTGGGGTTTGGGGTT[C/T]TAATGTAATACAATG	51317
rs768776752	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45949432	TGCTCCACTGTAGAC[C/T]GGATTTGCTGTTGTT	51317
rs768789850	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46042395	TGATAGTGCAACTCC[A/G]GAAAGTTCATCACCA	51317
rs768790943	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45993729	ACAGAGTCAGGCTGT[G/T]GAGATCCAAGGAAGT	51317
rs768802457	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932546	CTGTGCTAAAAAATT[A/G]TAACTACACGGCATT	51317
rs768816935	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46021768	GTTGCCCAGGCTGGT[C/G]TTGAACTCCTGGCTT	51317
rs768827249	snp	A/G	2.25233e-05	0.00335576	intron-variant	PHF21A	GRCh38.p7	11:45935742	TCTTCTTCTTTTGCT[A/G]AAAAAAAAAAAAAAA	51317
rs768838106	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46022128	TATTATAGAACAAAA[-/C]CATGTACTGTTTGTT	51317
rs768842505	snp	A/G	8.26016e-05	0.00642604	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953569	GGGTGCAGCAGGTGG[A/G]GTGATGGTGCGGCTC	51317
rs768858158	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46029445	GTAATCCTAATACAC[-/G]GGGAGGCCAAGGCGG	51317
rs768863033	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45951191	TAAATATGCCAAATA[A/G]TACATTATCAATTTA	51317
rs768891971	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46023645	CTTTATCCTCAGTTG[C/T]TAATGTGTGTTAAGA	51317
rs768896671	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46087295	AGGGTTTAACTTGAA[G/T]ACTGTAAATGTCAAA	51317
rs768898270	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46003135	AAAACAGGAGTAGAA[-/T]TAATTTCCTCAATAG	51317
rs768910111	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46116377	TCAGAAAGTTAGCAG[A/G]GTCAGTCAAAACATT	51317
rs768910741	in-del	-/AG			intron-variant	PHF21A	GRCh38.p7	11:46082613	TTAATATGAATAGTA[-/AG]AGAGTGTTTAGAATA	51317
rs768952694	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45967552	GGGCATAAGGCTTCT[A/T]TGCCAAGGTGGCTTT	51317
rs769010121	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46035134	TCCCAATATGTCCGC[C/T]CTCTTTTTGGCTTCA	51317
rs769036880	snp	A/C	1.65015e-05	0.00287237	intron-variant	PHF21A	GRCh38.p7	11:46076736	TTAAAAATATGCCCC[A/C]CTCCCCTTTTCCCCT	51317
rs769042629	snp	A/G	3.31395e-05	0.00407046	intron-variant	PHF21A	GRCh38.p7	11:45950286	ACAAAAGAAGAATAT[A/G]CTTCAGTCTGGGTTC	51317
rs769046406	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46071160	GTGGCTTCTTTTGGC[C/T]AATGAGATGTTAACA	51317
rs769053462	snp	A/C			missense, stop-gained, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934163	CAGCTGTTTTACCTT[A/C]TCCAGGGAGCTGTGC	51317
rs769063969	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46105429	CAGGAAGTAGCACAA[A/C]TGTAAATCTGGTTAA	51317
rs769089921	snp	G/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933717	TATTTCACTTGGCAT[G/T]GTGCTGGCAAAGAAC	51317
rs769098092	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46048852	TACATATACCTAGGA[A/G]TAACTGCTCAGTCAC	51317
rs769100021	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46034139	ATCTTTCACATATTT[A/G]CTGTCCACTGATGCT	51317
rs769100422	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45982232	AAAGTGCTGGGATTA[C/T]AGGCATAAGCCACCA	51317
rs769159524	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45970635	CGGTTAATTTGTGAG[A/T]TTCTTGAATATTTTT	51317
rs769180986	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46049237	AAGTAATACAGAACT[C/G]TCAGAGCCAGGCTTT	51317
rs769186489	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45998071	GAATATACATGTACC[A/T]CTGTGGAGAGAGGCT	51317
rs769199857	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45943778	ATAGAAACTATCTTA[C/G]GAGATGAAAGTTAAC	51317
rs769208810	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45960419	TGACTCTCAAAAACA[C/T]GCTAAGTGAAAGCAG	51317
rs769235437	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46100622	TGCCAAATAACATCA[C/T]AACATTAAAGACACA	51317
rs769258116	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46063221	AGAAGGAGCTCTTAC[C/T]ATTCTGTATACACCA	51317
rs769264764	snp	A/G/T			intron-variant	PHF21A	GRCh38.p7	11:46063467	CAAAAGCAGTCAGTC[A/G/T]TAGAGAATATGTAAA	51317
rs769271830	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46102362	AATTTAAAACCACTA[C/G]GAGAAATCTAAAAAG	51317
rs769278683	in-del	-/AA			intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119743	CGAACGTGGTCAGGG[-/AA]GAAAAAAAAAAAAAA	51317
rs769284550	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46072106	CTAATAAGGAAGACA[A/G]ATATTTAAAAAATAG	51317
rs769291430	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45942474	CAATACTTCAACTGA[C/G]AAAAAGTTGGGACAA	51317
rs769339237	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45960514	GAGACAGAAAGCAGA[C/G]TGGTGATTGCCAGCG	51317
rs769351233	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46100779	CTACCATTACCTTGT[A/G]GTGACTCCTAATGAA	51317
rs769354151	snp	A/G	0.000100942	0.00710358	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934033	AGGGGGAAGGGGCCG[A/G]CGTGGAGGTGGCGGC	51317
rs769359666	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46118181	CCATCACTTATACCT[C/T]CTAAAAATACAATTT	51317
rs769424171	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46010173	CTCTCCTGATATACA[A/C]TCATGAAGCAGTCTC	51317
rs769425506	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930228	AGGTGGCTGGAGAGG[C/T]AGCCGTGCATGCGGA	51317
rs769431356	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45959220	ACCCCACTACACACA[A/C]AAAAAAGGTTAACTA	51317
rs769455285	snp	A/C/T			intron-variant	PHF21A	GRCh38.p7	11:45998147	ACAAACCATTCTAGT[A/C/T]GTCTTTGTTTTAAAG	51317
rs769474102	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46102185	AACTCCTGAGCTCAA[A/G]TGATACACCAGCCTC	51317
rs769499928	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:46040893	CACTGACAGGAAGAC[-/AC]ACACACACACACACA	51317
rs769503438	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:46097828	CTCCCTAACTAGAAC[-/AC]ACACACACACACATA	51317
rs769505774	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45990757	TAGAGCAGTTTTAGG[C/T]TCAGAACAAAACTGA	51317
rs769511544	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46062653	TCTAGTGATTCTTGG[C/T]TATGTTCATATTTAA	51317
rs769542001	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46027408	GTCCTCAGTATTATA[A/G]TTCTGCACTCAATCG	51317
rs769552290	snp	A/G	1.65364e-05	0.0028754	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945948	ATGACTGGATTGGGG[A/G]GATGTTGGGGTAAGG	51317
rs769572671	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45991947	AACATGTAAACTGAT[G/T]ATTACATTTTGCAAG	51317
rs769584132	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46040693	TCCTGAAGCAGCTTA[C/T]ATGAAACTGCATACT	51317
rs769603864	snp	A/G	1.95112e-05	0.00312334	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965592	ATGTTATTCTGGGCC[A/G]CAGGCTTGGGTCGAA	51317
rs769624906	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46107622	GAGTGTATTCTAGGA[C/T]TAGAAAGGCTTTTTT	51317
rs769663249	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45938768	CTTAATATTTTCAGA[C/T]TGCAGTTGACTATGC	51317
rs769669377	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46055470	CATTCAGAATGAGGA[A/G]TGACAATTAAACCAG	51317
rs769684636	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46094528	ACAAACTACAATAAA[C/T]ACTAGCGAAATATTT	51317
rs769762612	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46054485	CCTGGGCGCCATTCT[C/T]GAAGATTCTGATTCA	51317
rs769765472	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45950679	AAGAGAAGGACTGGG[G/T]TCTACATCTTCTTTC	51317
rs769770389	in-del	-/CAACA			intron-variant	PHF21A	GRCh38.p7	11:46011852	TTTATTCTCTCTATG[-/CAACA]CAACAAAACAAAAAG	51317
rs769772586	in-del	-/AAAAA	0.0330046	0.124149	intron-variant	PHF21A	GRCh38.p7	11:45935742	TCTTCTTCTTTTGCT[-/AAAAA]AAAAAAAAAAAAAAA	51317
rs769772897	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46069194	AATATAAGCCAATAG[A/G]ATTTCACCAGGAGAA	51317
rs769782136	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45956307	TTTAACTTCTCTTTT[C/T]GTTTCCTATATGACT	51317
rs769820274	snp	A/G	0.00166898	0.0288393	intron-variant, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935227	GAGGGCCGTACGGAT[A/G]GGCCCACTCGCTCAG	51317
rs769835034	snp	A/G	3.29739e-05	0.00406028	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45950246	CCCTAGAGACACCAT[A/G]AAGGCAAGTTTCTGT	51317
rs769841386	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46002692	TTGGACTCTGTCCCC[A/G]TAAAATGTCCTATGT	51317
rs769855518	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45949678	TCACCTGCAAGACCA[C/T]GCTGTCCTACACGTG	51317
rs769879333	snp	G/T	1.85043e-05	0.00304168	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928847	CTGCCCGAGGCTGAG[G/T]CTGGGCCGGCGCTGC	51317
rs769888957	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45993821	TGCTGGGAAACGGGA[C/T]GGTCAGAGATGAGGC	51317
rs769917277	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46030784	CTTTAAGAAGGTGAC[A/G]ATCATTTCTTCTAAA	51317
rs769922875	snp	A/G	1.65941e-05	0.00288041	intron-variant	PHF21A	GRCh38.p7	11:45935601	TAGGTCTCTGCACCT[A/G]TGTATCGACTGCTGA	51317
rs769934758	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978869	TTTGCACAGCTACAC[C/T]AAGTTAGAATTTTAT	51317
rs769938535	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46096455	TGCCTCCCTCCATTC[C/T]TGTGAAGATCACCAA	51317
rs769943846	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45995055	CTGTACCTAAGCGTC[C/T]TAGAGTCTACTCTGC	51317
rs769968905	snp	C/T	1.64833e-05	0.00287078	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45936564	TGCTTCTTCCTTCTT[C/T]AGCATCTGAAAAGAT	51317
rs769985624	snp	A/G	1.65436e-05	0.00287602	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953581	TGGGGTGATGGTGCG[A/G]CTCTCTGTTTGTTTC	51317
rs770000076	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45970098	TTTACCCTATAAAAT[A/G]AACCAACCACACTTC	51317
rs770007484	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45954688	TTTATGAAGCTCTCC[A/G]TAAATACTGAAATAA	51317
rs770021049	snp	C/T	3.30038e-05	0.00406212	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971335	GAGAGGTAGTGTCTT[C/T]GTGGTAATCATAGAA	51317
rs770028867	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45977562	ATAAACATTTTCTGA[A/T]CAACCTGTACTTTGG	51317
rs770032368	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46111627	AAGGCACTGCCCTGC[C/T]TCTGCATACATTCAA	51317
rs770039643	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46009043	GCAGTGGCGTGATCC[C/T]GGCTCACTGCAACCT	51317
rs770053512	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46072564	CAGAAATTAAGTTTT[C/T]CCTGTTTACATTACT	51317
rs770055107	snp	C/T	1.69861e-05	0.00291424	intron-variant	PHF21A	GRCh38.p7	11:45938145	CTCCCCTGTTGGACC[C/T]ACCCACAGTACCTGG	51317
rs770063157	in-del	-/AAA			intron-variant	PHF21A	GRCh38.p7	11:45939772	AGGAGAACATAGCCC[-/AAA]AAAAAAAAAAAAAAA	51317
rs770079017	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45946760	CTTTAATGATTCTCA[C/G]TTCCCACAAACTGAT	51317
rs770089281	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46043664	CCACTTTTAGAAGTC[A/G]GCAGCTTTTTCCTTC	51317
rs770093745	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45953196	ACAGAACACAGTAAT[C/G]ATTAGGAATGTAATG	51317
rs770113422	in-del	-/TGTGTGCGTGCA			intron-variant	PHF21A	GRCh38.p7	11:46021523	CCCTTATTGCACATG[-/TGTGTGCGTGCA]TGTGTGTGTGCATGT	51317
rs770127878	snp	A/G	1.69648e-05	0.00291241	intron-variant	PHF21A	GRCh38.p7	11:46079114	TTTAACAATTAAATG[A/G]ATAACAATAGTAGTT	51317
rs770165205	snp	A/G	1.88549e-05	0.00307036	intron-variant	PHF21A	GRCh38.p7	11:45935756	TAAAAAAAAAAAAAA[A/G]AAAAAAAAGGAACGG	51317
rs770175280	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45935458	ACCTACCAACTGGCC[A/G]CCTGTACCTGAGGTC	51317
rs770184273	snp	C/T	0.000792511	0.0198904	intron-variant	PHF21A	GRCh38.p7	11:46076743	TATGCCCCCCTCCCC[C/T]TTTCCCCTACCTGTT	51317
rs770191738	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46059350	CTGAAGAATAATTGA[A/G]AATGTAAAGAAATGC	51317
rs770201916	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45942071	CAAACATACAGAGAC[C/T]TGTGTGTTGATTTTA	51317
rs770213284	snp	A/G	4.03242e-05	0.00449004	intron-variant	PHF21A	GRCh38.p7	11:45965300	GCCCAGAGCAGGTAC[A/G]TACTCTGCCTGTACC	51317
rs770222072	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46054545	GATTTTTCAAAAGCT[C/T]TTCATTTTATTAGGG	51317
rs770224073	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46018916	ATGCAATCCAATGCA[A/C]GACTTTTTATGACAA	51317
rs770233815	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45968808	GGTGGCACATGCATG[G/T]AATCCCCAACTACTT	51317
rs770244959	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46036319	CCTGAGTCTAAGATG[C/T]CAGTACGACACTGAA	51317
rs770247940	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46083082	TATTCAACACACCTC[C/T]ATGTTAAACTAATTT	51317
rs770288295	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45964736	TGTATGTCTCTAGCC[A/T]CGTTTTTTAAGATAA	51317
rs770319558	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45984447	GCCTCTGACACTTCA[A/G]GTCACAGTTTCCAAG	51317
rs770334972	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46035420	TCTAGTATGTTTTGA[C/G]TCTGTTGGTTACTTC	51317
rs770354009	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46036665	TTTCTTGCTTTTCTG[A/C]CTCGACCATTTTTTC	51317
rs770380509	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46000343	ACTTCTTCATACTCT[A/G]CTGAGAGTTGCAGGA	51317
rs770381162	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46050087	CAGCAGAGTTAGCGA[C/T]TGCCACTAGGGATTG	51317
rs770409396	snp	A/C/G			intron-variant	PHF21A	GRCh38.p7	11:46104809	CCAGTGACCAGCACA[A/C/G]TGGTATGCAGCACGT	51317
rs770443412	snp	A/G	1.65247e-05	0.00287438	missense, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934194	ATCTCCTTCTGCCGG[A/G]CCAGGATGGTGTTCT	51317
rs770468361	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46015741	ACACAGGGTCACAAT[C/T]ATCAATATTACTGTC	51317
rs770470826	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46102064	GGTTTCATCATGTTG[A/G]CCAGGATGGTCTCAA	51317
rs770480350	snp	A/C/G	9.89299e-05	0.00703244	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946056	GGAGGGAAAGAGAGG[A/C/G]GGAAAATGATCTTAC	51317
rs770491044	snp	A/G			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46123192	GTCATTCGCAGAACC[A/G]GAAATAGCCTTGGAC	51317
rs770551672	snp	A/C	1.6552e-05	0.00287676	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946070	GGGGAAAATGATCTT[A/C]CATACCTTTGGCCAG	51317
rs770568216	snp	C/G/T			intron-variant	PHF21A	GRCh38.p7	11:45962242	ATCATCTAAAGGGAA[C/G/T]AGCAGAAAGCAAAAG	51317
rs770571530	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46051888	ACCAGGAGCCTCTTG[A/C]AATGGTTGGAACAGT	51317
rs770578228	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46102622	TTAAGTAACATGCCT[A/G]CCTCTTCCTCAACTT	51317
rs770594300	snp	A/C	1.65154e-05	0.00287358	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46079160	GCTTCATTTGAGCAA[A/C]CAGTTTCTGGTAATA	51317
rs770596077	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45984529	GTTCACACGACAGCA[A/T]GACAGATCCTGAAGA	51317
rs770641187	snp	C/G			downstream-variant-500B	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45929127	GTTTGGGGGAGCAAG[C/G]GCACTCTGGGGCTAG	51317
rs770664720	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46071249	CTTAGGTAAACTACA[A/G]AATGAATACGCCCCA	51317
rs770666758	snp	G/T	3.34459e-05	0.00408924	intron-variant	PHF21A	GRCh38.p7	11:45971109	TGAGGAGCAGCTGCT[G/T]GCTTACCAGAGTGAC	51317
rs770685539	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46014043	AGATTCAAGGGGTAC[A/G]TGTGCAGGTTTCTTA	51317
rs770704025	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45977237	TGTTGCCCGGGTTCA[A/G]GTGATTCTCATGCCT	51317
rs770717924	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46077787	TACATGATCACCAAC[C/T]ATAACAGAAATGATA	51317
rs770729838	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46029373	TTTTATTCTATATTC[C/T]CTTTGAGTTTAAGGA	51317
rs770747370	snp	A/G			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46049437	TAGCTTCAACACAGT[A/G]TATTCCTGTACAGTG	51317
rs770748050	snp	C/G	1.65228e-05	0.00287422	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945955	GATTGGGGGGATGTT[C/G]GGGTAAGGGCTCCAA	51317
rs770758953	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45992078	CAACTGGAGAGGCAG[G/T]GCCCTAATAACACTA	51317
rs770781297	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45952121	AAATTTTTGATGATA[C/G]AATAAAAAGCTGTCA	51317
rs770796323	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46003592	GGCAGAGTGAGAAAA[C/T]GCTACAATTCTCACT	51317
rs770807965	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46094614	CATGAAATCCTGGCC[A/G]TGCACAGTGGCTCAT	51317
rs770811899	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46058021	TTTTCCGTCAGTTAA[A/G]TTTCCAACCTGGAGA	51317
rs770819420	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46027694	AGACTAACACACAGA[A/G]CTATGAGAAGACGCC	51317
rs770880517	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46035158	GGCTTCAGCTAGTTT[A/G]AGCTGAATGTGTAAT	51317
rs770885566	in-del	-/CAATTCCAGT			intron-variant	PHF21A	GRCh38.p7	11:45954395	TCTCCTATTTCGGAA[-/CAATTCCAGT]CATAATCTCAGAGAG	51317
rs770905187	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46041469	TCAAATGTATATTGG[A/G]AAACTAAGGGGTAAT	51317
rs770994397	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46106509	GGGTTGGGGGAAGTA[A/C]ACAAATACTAAATAG	51317
rs770995462	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46068458	TTGGCTCCTAAAAAG[C/T]ATTCGTTATTCACAC	51317
rs771067349	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45940446	TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT	51317
rs771087186	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46067021	CCTCATTATTTTTTA[A/C]CAGCTACATGTTATT	51317
rs771093415	in-del	-/TA			intron-variant	PHF21A	GRCh38.p7	11:45947131	GAGACCTGATTTGTG[-/TA]AGAGCATTTTGACTC	51317
rs771094000	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46081344	ACTGAAACACAAGGT[G/T]TTATACACATACATT	51317
rs771108253	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46045858	TGCTCATGGTTTACC[C/T]TGAGATGTGGTCACC	51317
rs771117752	snp	A/C	1.90242e-05	0.00308411	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928853	GAGGCTGAGGCTGGG[A/C]CGGCGCTGCCCCTCA	51317
rs771127315	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46083217	CTTAAAGAAGCCCAC[A/G]TGCATAGGGCCAACT	51317
rs771127519	snp	G/T	3.2981e-05	0.00406071	intron-variant	PHF21A	GRCh38.p7	11:45935626	TGCTGAAGGCATGAG[G/T]TTTACTTACACTTAT	51317
rs771128026	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45996691	TTTGAAAGTAGGTGT[A/T]GGCACAATTAATCTT	51317
rs771138750	snp	G/T	1.65603e-05	0.00287747	intron-variant	PHF21A	GRCh38.p7	11:45936606	TACCTTGAGAAGGAG[G/T]TTTAAACACACATCC	51317
rs771148348	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46033364	CTGCCTCCTAGGCTC[A/G]AGGGATCCTTCCACC	51317
rs771154244	snp	G/T	3.29451e-05	0.00405851	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45949449	GATTTGCTGTTGTTC[G/T]TCTTTTTCGCTCTTG	51317
rs771170218	snp	A/C	0.000139799	0.00835942	intron-variant	PHF21A	GRCh38.p7	11:45971397	AAACAGATATTAGGA[A/C]ACTAAATCTAAACTA	51317
rs771179559	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46097529	GAGCAAAAGAATACT[A/C]AAATAAAGACTAAAA	51317
rs771186046	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46061310	CTGTTTTGATCCCAT[A/G]TGAATCTTAAAATAG	51317
rs771216009	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45995542	TTGGTGCAGGTAGAG[C/T]GAGATAGAGTGGTTG	51317
rs771217709	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45936976	TCAATTTTAGATTTC[C/G]ATGTCCCTCAAAGAC	51317
rs771228626	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46109980	GCAAGACTCCGTGTC[-/A]AAAAAAAAAAAAAAA	51317
rs771240060	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46032347	TTTATATAACAATCT[A/G]GGATCATACACTGCA	51317
rs771261232	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46010204	TGGGCATTTCTAAAG[-/A]AAAATTAATAATGGA	51317
rs771261872	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46046474	CAAGAAACCAGAGCT[C/T]GTCATACAGGGCAAG	51317
rs771263963	snp	C/T	1.65444e-05	0.00287609	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965417	CTGGGCCATGGGGAA[C/T]GTTTTGGCTATGGTT	51317
rs771265757	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45963422	TAAAACTCTGTGTCA[-/A]AAAAAAAAAAAAAAA	51317
rs771282720	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45939007	CCCGACTAATTTTTT[A/G]TATTTTTAGTAGAGA	51317
rs771286788	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45964496	CAGAAGATTCAGGAT[C/T]ACCACAGACTATTTT	51317
rs771310265	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46009191	GATAGCCAGGCTGAT[C/T]TCCAACTCCCGACCT	51317
rs771313972	in-del	-/CACCTGCCAC			intron-variant	PHF21A	GRCh38.p7	11:45938978	AGCTGGGACCACAGG[-/CACCTGCCAC]CACCCCCGACTAATT	51317
rs771353839	snp	A/G	1.6898e-05	0.00290667	intron-variant	PHF21A	GRCh38.p7	11:45938152	GTTGGACCCACCCAC[A/G]GTACCTGGTCCTGAC	51317
rs771358428	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46082371	ACCCCTACCTTGATG[C/T]CATTTCTGGCATGCC	51317
rs771402560	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46023935	CACTCCATCCTGGGC[A/G]ACACGGCAAGACACC	51317
rs771403384	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46115093	TGCCTTCAACTGAGA[C/T]ATTTTCACCAAAGTC	51317
rs771410575	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45996038	AACCTCAAACTCCCC[A/G]GCTCAAGTGATCCTC	51317
rs771417826	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46043912	ACAGTAAAAGATGGA[A/T]CGCAGCAACTGCTTT	51317
rs771437440	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46113953	CCCATATTCTAATAT[C/T]GCCCACCAGGAAATA	51317
rs771442018	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46024897	TTCTATACCATAGTG[A/C]CTCCTAGTTCTAGAC	51317
rs771446500	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46079968	GCTGCCCAAAGTTAA[C/T]AATAACCATAGACAG	51317
rs771469180	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45971967	GCATGTCGCCTCTGA[G/T]GTAGTTACCCTGGAG	51317
rs771491417	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46113622	ATTACGAGATCAAGA[A/G]ATCGAGACCATCCTG	51317
rs771498407	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46025157	ATATGTTGAAAGAAA[A/C]TAATTTTCTCTGGGG	51317
rs771527707	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46038182	CTCAGGCTGGAGTGC[A/G]GTGGCACAATCTCAG	51317
rs771552967	snp	C/T	1.65192e-05	0.00287391	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084221	GTCTGCAACTCCATC[C/T]TCTACCTTCTCCACT	51317
rs771556381	snp	A/G	1.65781e-05	0.00287902	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084243	TTCTCCACTTTCTCT[A/G]CTAATTCTATAGTTT	51317
rs771558979	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45970345	TGGTTGAGTGACCTC[A/G]TTGCTTCTCTAAGGA	51317
rs771560407	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46066120	AAATAAGCCAGACAG[-/A]AAAAAAGTAGGCTCT	51317
rs771565539	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46074792	ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCAATAA	51317
rs771603970	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46112390	CTAATTCTAAACGTT[G/T]ACTGAGCCCTTATTA	51317
rs771651902	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46106092	ATTGCAGCTCCCTCC[A/G]TTGACATCGTAAAGT	51317
rs771653282	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46072942	AAGTGCTTTGGCTCC[A/G]TATCAGAATATCTCC	51317
rs771680389	in-del	-/AAG			intron-variant	PHF21A	GRCh38.p7	11:46079652	CCACTGTCTTCTCTC[-/AAG]AAGGAGTTCGGTGCA	51317
rs771682088	snp	G/T	1.66726e-05	0.00288722	missense, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934215	ATGGTGTTCTTCATT[G/T]CCATGCATTTCTGCA	51317
rs771700814	snp	G/T	1.64833e-05	0.00287078	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971312	GTCGCAGTTGCTGCT[G/T]TCAAGACGAGAGGTA	51317
rs771701056	in-del	-/ATAAAA			intron-variant	PHF21A	GRCh38.p7	11:46108585	TATATATATATATAT[-/ATAAAA]TACATATGTAAATGC	51317
rs771717351	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45946337	TTTCTAGTGCAAGAA[C/G]CAAGATGTCAAAGCC	51317
rs771724553	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46039092	AAGGATGGGTTGTGG[A/G]GTCTGACAGACAACT	51317
rs771740815	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45970836	CATAAATGAAACAGT[A/G]TGTATGCCTCTGTGA	51317
rs771762693	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45947656	CCAAGGTCTTTCTGG[A/C]TCATTTAACCCCTGT	51317
rs771768027	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46041764	TAAATCAGATACCTA[C/T]ATACCCTTCCACGCT	51317
rs771768590	in-del	-/T	4.97896e-05	0.00498922	intron-variant	PHF21A	GRCh38.p7	11:46079091	TTTTATTTTAAATTA[-/T]TTTTAAATTTAACAA	51317
rs771769835	snp	C/T	0.000185684	0.00963366	intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935149	CTCTAGAAAGCCCGC[C/T]TCCTCACACTGGTCA	51317
rs771785246	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46089939	CCTTCACAAGTCTGT[A/G]TAGTGTCCTGGACCC	51317
rs771803328	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45962347	CTTCCATGGCTACAT[A/G]CATTACATTGTTTTA	51317
rs771806973	in-del	-/AGCAAC	1.64743e-05	0.00287	intron-variant	PHF21A	GRCh38.p7	11:45948846	CACACACAAAGCAAA[-/AGCAAC]AGCAACAGCAGCAAG	51317
rs771824053	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46000834	CTGAGGCAGGAGGAT[C/T]GCTTGAACCCAGGAG	51317
rs771836226	snp	A/G	1.75888e-05	0.00296548	intron-variant	PHF21A	GRCh38.p7	11:45946104	TCCTCATTGGCTAGC[A/G]TGGAAAAGGAAGTGA	51317
rs771852591	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45964762	GATAAAATCTGACTT[C/T]AGGAAATATAAATGA	51317
rs771862291	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46030614	TGAACACAAAATTCA[A/G]AAAGATTCTTTAATC	51317
rs771910736	in-del	-/CT			intron-variant	PHF21A	GRCh38.p7	11:46007229	TGAGAAAAGGGCCCC[-/CT]GTCTTTTCAAGGAAT	51317
rs771921762	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46079546	CCCCACACAAAACCG[A/G]CCTGTTCATACACAG	51317
rs771982973	snp	A/C	1.656e-05	0.00287745	intron-variant	PHF21A	GRCh38.p7	11:45950282	AGAAACAAAAGAAGA[A/C]TATGCTTCAGTCTGG	51317
rs772021138	in-del	-/AAC			intron-variant	PHF21A	GRCh38.p7	11:46065732	TTACTCCTTTTCTTT[-/AAC]AAAAGTTGTTTAAGC	51317
rs772024741	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46101618	GAAATGCCTGGTATA[G/T]ATCTTAGAAGCTACT	51317
rs772034560	snp	G/T	1.65124e-05	0.00287331	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971150	GCCACAATTTGGACA[G/T]CCTCTGCCCCAGGCC	51317
rs772037178	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45978571	TTCTCTCTATATAAA[A/G]ACACAGTGAAGACCT	51317
rs772058135	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46029496	AGTTCAAGACCAGCC[A/T]GGGCAACATGGTGAA	51317
rs772068162	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46017852	TAGCCACCCAAATTG[C/T]TCTTATTACTTTGCC	51317
rs772068987	snp	C/T	6.60186e-05	0.00574499	intron-variant	PHF21A	GRCh38.p7	11:45935614	CTATGTATCGACTGC[C/T]GAAGGCATGAGGTTT	51317
rs772074298	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46058780	TTATTACATTCTCTT[C/T]ACAAAATCTGGAACA	51317
rs772122372	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45990972	ATATAATGACATACA[A/G]CCACCATTATACTAT	51317
rs772126934	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45977455	TTTGATTTTTATAAC[A/G]TAAAATGTTACTTGA	51317
rs772133757	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46018250	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	51317
rs772144840	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45950968	TCAATCACACATGAA[C/T]CTAAAAATTATGGAG	51317
rs772145492	snp	A/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118926	TGTAAACAAATATCA[A/T]AAACACTGAAAAGTA	51317
rs772152315	in-del	-/CACACACACACACACG			intron-variant	PHF21A	GRCh38.p7	11:46040920	ACACACACACACACA[-/CACACACACACACACG]CACGCACAATTAAGG	51317
rs772160635	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46090179	AGTAAGGTATGAGAG[C/T]ATAGTGACAATGAGG	51317
rs772173184	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45966487	CTCACTAAAAACAGT[C/G]AAAAAAAGTTACAGT	51317
rs772173645	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093238	ATTTAAACTCCACTA[C/T]ATGCTATGCTCTAAA	51317
rs772189942	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46055771	CATTTATAAGTTACA[C/T]AGCAGGGGATTCATT	51317
rs772200573	in-del	-/GTGTGTGTGC			intron-variant	PHF21A	GRCh38.p7	11:46030811	TAAACCACATAGTGT[-/GTGTGTGTGC]GTGTGTGTGCGTGTG	51317
rs772205797	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46068530	AGTCCCTAAACATTC[C/T]GAAATACAGATATGT	51317
rs772212782	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46005748	ATAATATTTGTAGCA[A/C]AATTAAGCTTCCATA	51317
rs772216470	snp	C/T	3.31345e-05	0.00407016	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953543	TGAGGGTTCTCCTCC[C/T]GTTTTGGTTTGGGTG	51317
rs772244666	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46033547	GGGATTACAGGTGTG[A/C]GCCACCATGCTTAGC	51317
rs772267768	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46069401	TTTCCATCACAATGA[C/G]AAGATTTCTAAGACA	51317
rs772268825	snp	G/T	1.65444e-05	0.00287609	intron-variant	PHF21A	GRCh38.p7	11:45979987	AAATGAAGACAAAAA[G/T]AAATAAAAGATATTA	51317
rs772302834	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46004773	GACTAAAGGACTCAT[C/G]ATCTAAAAGATGTCT	51317
rs772315953	in-del	-/TTG			intron-variant	PHF21A	GRCh38.p7	11:46083913	AGATTTCTTTCTTTT[-/TTG]TTAACACCTTTGGTA	51317
rs772324325	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:45991558	CTGCAGTAAGCTTAT[-/AC]ACACACACACACATG	51317
rs772356797	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997844	AACCTCCCTCACCAG[C/T]AATAGGTCCTCTTAT	51317
rs772392027	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46019898	AAAGCCCATATGCTT[A/T]ACTTTCAGGGTTCCT	51317
rs772448272	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997064	AAAACTATCACAAAA[C/T]CTTGGTTTTGAAAAT	51317
rs772466588	snp	G/T	1.64852e-05	0.00287094	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979816	GGGCGTGGTGGTGGT[G/T]GTACTGCTGCTGTTG	51317
rs772488190	snp	A/G	0.000138615	0.00832395	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928907	GGCAACCTGCCCTCC[A/G]CCATCCCTGCTATTT	51317
rs772499684	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46111164	TTTGCTATATAAACA[A/G]GTACTTTAAAAAATA	51317
rs772509051	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932361	CCCTGATACCATCCA[C/T]GCTTCCATTTGGGCT	51317
rs772515299	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46026294	TTTGTAGTAAAATGT[A/G]CCTTAGGGGGAAACT	51317
rs772521775	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46009374	CTACCTTTGAGGGTT[A/C]TGACACATTCCATTT	51317
rs772526475	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45942004	CTAGAAATGCCTGCC[C/T]CTCAAGTGTTATTGT	51317
rs772532230	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46100380	TTATAAATAACGTTA[A/G]CTATTTGCTATTTCC	51317
rs772566668	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46098657	AAATCACTCCTTATC[C/T]CAAGACAACTCAAAC	51317
rs772583830	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46046217	AGTGAATAGCAGCAG[C/G]AGAAATCCAGGTCCA	51317
rs772600228	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46010695	CCAGCGTGCAAAGCC[C/T]TGACCCACAGAAGTT	51317
rs772602190	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46028942	ATGCCCCAAAGGACT[A/G]TATGAACACAAGTTG	51317
rs772614999	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46061378	AATAGGAATAGCATT[G/T]AATCTGTAAATTGCT	51317
rs772615464	snp	C/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45930277	ACACGGTCACCCTCA[C/G]GGAAACAGCTGTGTG	51317
rs772620179	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46098866	AGGAGGAGGATCAAC[A/G]CCCAGCACTGCATCT	51317
rs772643050	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46115311	TAAGACTGAATTGAG[A/G]GACAAGTAATAGAAA	51317
rs772685816	snp	C/T	1.80543e-05	0.00300447	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965545	TAAGCTGAGGAGCTG[C/T]GAGCATGGGAGGTGG	51317
rs772700844	snp	A/G			missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979888	TGTTTTCAGATTGTG[A/G]CAATGGCTGTATTTG	51317
rs772704707	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46026539	AAGCTTTAGCTACCT[C/T]TTCTCTACCCTGTTC	51317
rs772707430	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45942925	TCCCTCCTCAGATCT[G/T]CTCCTCTCTTAATCT	51317
rs772716619	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46069907	CCAACAATTTCCTTT[C/T]AAACAGAACTCACCT	51317
rs772717160	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46014473	TGTGGCAATGAACAT[A/G]CAAGTGCAAGTGTAC	51317
rs772733580	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46102436	AAGATCAATATATAA[C/T]AAGGCATCAGTGGTA	51317
rs772740423	snp	A/G	3.30573e-05	0.00406541	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945952	CTGGATTGGGGGGAT[A/G]TTGGGGTAAGGGCTC	51317
rs772742543	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46047685	GGCAGTGACTAACAA[C/T]CAGAAAGCCTGAGAT	51317
rs772754445	in-del	-/A	2.03813e-05	0.00319222	intron-variant	PHF21A	GRCh38.p7	11:45969907	TTGCCTGAACCTGCT[-/A]AAAAATGAGGAAGAT	51317
rs772773440	snp	C/T	1.67049e-05	0.00289002	intron-variant	PHF21A	GRCh38.p7	11:45938322	ATCACCCTATAAAGT[C/T]GAGAGGAAAGGTAAG	51317
rs772775116	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46012219	CCCTCAGAAAGTATT[A/C]AAATCTTTGTCTTTC	51317
rs772802768	snp	A/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085695	CAATAAGATTCATGA[A/T]CTTCATATTTCTAAA	51317
rs772821474	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46100952	AAGTGAAACAAGCAT[C/T]CCTTAACCAATACAC	51317
rs772841107	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45999203	TGTAAACAGAGAAGA[A/G]AGCAGTAAATAGAGA	51317
rs772845561	snp	C/T	1.64931e-05	0.00287163	intron-variant	PHF21A	GRCh38.p7	11:46076744	ATGCCCCCCTCCCCT[C/T]TTCCCCTACCTGTTT	51317
rs772907449	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46116733	CTTTGGGAGGCCAAG[C/G]CAGGTGGATCACCTG	51317
rs772957304	snp	C/T	1.99209e-05	0.00315596	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965598	TTCTGGGCCACAGGC[C/T]TGGGTCGAACCTATA	51317
rs772992239	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45973912	TCAATGTACTTTTGT[C/T]TCAAGTAAATCATCA	51317
rs773034566	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46010961	CTCCTCTGTATAAAA[A/T]ACTTTCTCTTTCTCT	51317
rs773045696	snp	A/G	1.67897e-05	0.00289733	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45969835	GAAGAAAGTTTGGAC[A/G]TGGAGTGAGTCTAGG	51317
rs773059672	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46041159	CTCTTTCCCCATAGC[C/T]CACCACCACAGTTTC	51317
rs773103093	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46077708	CAATGAGATCACCCA[C/T]ACCTGTTGTCCAACA	51317
rs773105061	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46062710	GCTAGAACTCTCATA[C/T]ACTACTGAAAGGAAT	51317
rs773121416	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46034866	CTGGCCACACAAATC[A/C]AAGTACTTCCTCAAG	51317
rs773122851	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46026798	ATGCGACATTCTGTC[A/C]CACATGACTCACCCA	51317
rs773126783	in-del	-/A	1.65111e-05	0.0028732	intron-variant	PHF21A	GRCh38.p7	11:46079174	CCAGTTTCTGGTAAT[-/A]AAAGAGAGAAAAAGA	51317
rs773140239	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016544	AGATCAAACACCATT[C/T]CTTACATAAACCCTT	51317
rs773144122	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46032430	CCATGTGAAAATCAG[G/T]ATCATCTACTTCCTT	51317
rs773145495	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46039773	GGATCTCAGTCAAAA[C/G]TGCACAATCTGCAGC	51317
rs773149369	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45990804	CCACATACTCCTGGC[C/T]TCCCCACCCCACATC	51317
rs773176413	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45983290	GCAAACTTACATCAG[C/T]CCTTGAGAGGAGGGA	51317
rs773193373	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46076413	GACAGGTAACAAGGT[A/G]CACGCAGCACCTACA	51317
rs773196416	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093162	TTTAGGTTTTGGGAT[C/T]CCAATCCAATATTAG	51317
rs773209259	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46068856	AACTCAGCAAACTGA[G/T]GCATCTGGTACAAGT	51317
rs773230662	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46030840	GTGTGCGTGTGTGTG[C/T]GTGTGTGTGTGTGTG	51317
rs773234242	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46066367	TTTATCTGTATGGTA[G/T]ACCTCAACAGTTTTT	51317
rs773243359	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46004442	GAGACACTGGGGAGT[A/G]GGGAAGGGGTAGAGG	51317
rs773255017	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45995147	TTCAGGTTGGCTGCT[A/C]AGGCAAGTGTGATAG	51317
rs773291494	snp	C/T	3.31664e-05	0.00407211	intron-variant	PHF21A	GRCh38.p7	11:45935602	AGGTCTCTGCACCTA[C/T]GTATCGACTGCTGAA	51317
rs773332364	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46065472	TGACCAGAATGAATA[C/T]GGGTCCTGATAGTGT	51317
rs773342340	in-del	-/AGGAA			intron-variant	PHF21A	GRCh38.p7	11:46079852	GAAAGGAAAGGAAAG[-/AGGAA]AGGAAAGGAAAGGAA	51317
rs773345019	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45949681	CCTGCAAGACCACGC[C/T]GTCCTACACGTGGTT	51317
rs773348693	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46058963	AGATGAAGAGACACA[A/G]GAGACAGAGACTCCA	51317
rs773349314	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45971906	TTTTTTTTTTTTTTA[-/A]TGGTGTCACCCTGGA	51317
rs773364702	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46090942	ATTTGCAACCTCTGG[C/T]ATAAATGGGTTAAGG	51317
rs773390106	snp	A/G	1.72409e-05	0.00293601	intron-variant	PHF21A	GRCh38.p7	11:45971388	AGACAGGGAAAACAG[A/G]TATTAGGACACTAAA	51317
rs773420254	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46079890	GGAAAGGAAAGGAAA[A/C]GAAAGGAAAGGAAAG	51317
rs773431870	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45977749	AATTTATGTAGGCTG[C/T]CCTAGCTATCTGATT	51317
rs773450851	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:46092028	GTATAGCTACGTGAA[-/AT]TAGACAATTCATTTC	51317
rs773461665	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45953305	TTTTCCTTTGATACA[A/G]TCAAAATGCCTATGT	51317
rs773463801	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45995045	AATTGTCAGACTGTA[C/T]CTAAGCGTCCTAGAG	51317
rs773482080	snp	A/G	1.64792e-05	0.00287042	intron-variant	PHF21A	GRCh38.p7	11:45948992	TTGAGTAGTGTGGTT[A/G]TTACTAATACTGGCA	51317
rs773493010	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46029874	AACAAAGGCATAGAA[C/G]AAGATAAGAATGTGA	51317
rs773515169	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46076261	ACCGAAGTTTTTTCA[C/T]GTAATAGTAGGTCAA	51317
rs773524052	snp	A/G	1.65471e-05	0.00287633	intron-variant	PHF21A	GRCh38.p7	11:45935757	AAAAAAAAAAAAAAA[A/G]AAAAAAAGGAACGGT	51317
rs773541231	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45935519	GCCCAAGTTAATCAC[A/G]TTAATAAACAGAAGG	51317
rs773546299	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45954692	TGAAGCTCTCCGTAA[A/G]TACTGAAATAATTTT	51317
rs773558284	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46096620	TCTTTCCCAACTCTC[C/T]GGCTACTCTCTTTGG	51317
rs773560230	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46110177	ATAAAGTACATTCAT[A/G]AGTATTATCTTATCT	51317
rs773564577	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:45991572	TACACACACACACAC[-/AT]GCACGCGTGCACTTT	51317
rs773578855	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46059556	TCAGCTTCCCAAGTA[A/G]CTGGGACTACACACA	51317
rs773582616	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46071381	TGAAGCAGAGGTGCC[G/T]GGCCAAGTACAGCCT	51317
rs773590062	snp	A/C	1.64762e-05	0.00287016	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971195	GACGTCTGGAGGTTG[A/C]CTGGTGTGTTCTGCA	51317
rs773612103	snp	G/T	1.64969e-05	0.00287196	intron-variant	PHF21A	GRCh38.p7	11:45936577	TTCAGCATCTGAAAA[G/T]ATTTTTAGAATTTTA	51317
rs773613191	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46036449	TCTGTCAAATTCCCC[A/G]AAATATTCACTGGAA	51317
rs773755465	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:45955286	CTTTCTCTCTCCAAC[-/AC]ACACACACACACACA	51317
rs773755538	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46058220	TATTCTTAGATGTCA[A/G]GTATTATAACCTCAC	51317
rs773773637	in-del	-/GGAAA			intron-variant	PHF21A	GRCh38.p7	11:46079831	GAAGCCCAAACAAAT[-/GGAAA]GGAAAGGAAAGGAAA	51317
rs773788697	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46055142	GAGAACTTAAGATAC[-/T]TTGAAGCAATCTGAA	51317
rs773798520	in-del	-/TATT			intron-variant	PHF21A	GRCh38.p7	11:46108123	GCCCCAATTCTTGCC[-/TATT]TACTTTGTAAATGTG	51317
rs773812465	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46072824	CCGAAGCTGCAACCA[C/T]GATGGCTTAACCCTG	51317
rs773855356	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46041392	ACTTCTTTCGAGCAA[C/T]AACATTTTTTGTTGC	51317
rs773888687	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46106353	AACTCTCTAACAGCA[A/G]TAATTACAATATGTT	51317
rs773891104	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46035630	CAACCAACAGGTGGA[A/C]CTAACCTAATCTATA	51317
rs773893667	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46023986	AAAAGAATCACTGAA[G/T]GGCATAGAGCATGTA	51317
rs773900885	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45984506	ACATTCAGCGATACT[A/C]TCAACGTGTTCACAC	51317
rs773913744	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45999300	CAAGGAAACTTTTTT[C/G]AGATTAAAAATAAAA	51317
rs773959586	in-del	-/TATA			intron-variant	PHF21A	GRCh38.p7	11:45956672	CACTAAGAAAATAAT[-/TATA]TATATACAGAAACAG	51317
rs773962478	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46102805	GAGGGCCCAAAGTAG[A/G]GGGTATCCCCACAAA	51317
rs773965504	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45946171	GAAGGAAGAGAAGCA[A/G]AGATTTAAATGTCAT	51317
rs773977748	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46036669	TTGCTTTTCTGACTC[A/G]ACCATTTTTTCCACT	51317
rs773978594	snp	A/C	3.30246e-05	0.0040634	intron-variant	PHF21A	GRCh38.p7	11:46079176	CAGTTTCTGGTAATA[A/C]AGAGAGAAAAAGAGC	51317
rs773991430	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46065537	TCTCCTTATTTGAAT[C/G]AATAAATTCACTTAC	51317
rs773992294	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46088196	TTCTAACAAGTTATA[A/G]ATAACAAATCAGTTG	51317
rs773998675	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45969057	TTATCTCATATTAGC[A/C]CTGCCCATCCTTCTC	51317
rs774002404	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45985549	AGTCCAGGCAAGACA[C/T]AGGATAGAATTCTAA	51317
rs774003990	snp	G/T	1.64982e-05	0.00287208	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934124	TACAGGTTTGGAGAG[G/T]TCGATGCCGTGGATG	51317
rs774005618	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46014047	TCAAGGGGTACATGT[A/G]CAGGTTTCTTATAAC	51317
rs774010372	in-del	-/AAGA			intron-variant	PHF21A	GRCh38.p7	11:45962902	TGTCTCAAAAAAGAG[-/AAGA]GAGAACATGAAATTT	51317
rs774042476	snp	A/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118803	GTTTCCAACAATGCT[A/G]TAAACCAAATAAATT	51317
rs774074315	snp	C/T	0.000158143	0.00889081	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965337	TCAAGACTTGGCTTG[C/T]TAAGCTGTACAGTTT	51317
rs774104118	snp	A/G	1.6519e-05	0.00287388	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945956	ATTGGGGGGATGTTG[A/G]GGTAAGGGCTCCAAA	51317
rs774138116	in-del	-/TCAAGCAATCTTCTCACT			intron-variant	PHF21A	GRCh38.p7	11:45980609	CTTGAACTCCTGGCA[-/TCAAGCAATCTTCTCACT]TCAAGCAATCTTCTC	51317
rs774161941	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46050253	CACACAGACTAATGT[C/T]GCCAGCAGCATTCCA	51317
rs774167900	snp	A/G	3.29717e-05	0.00406015	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46076770	TGTTTCTCACTCAAA[A/G]CTGTGATTTTGGCTT	51317
rs774168704	snp	C/T	1.65748e-05	0.00287874	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971125	GCTTACCAGAGTGAC[C/T]GTGTTTTTTGCCACA	51317
rs774181412	snp	C/T	1.70977e-05	0.00292379	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45969869	GGGGATAAACTGTGG[C/T]ACTTTGATGGGCTGA	51317
rs774192349	snp	C/G	1.67335e-05	0.00289248	intron-variant, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946082	CTTACATACCTTTGG[C/G]CAGTGTTCCTCATTG	51317
rs774192443	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45957105	AGTTATAATCATATA[C/T]GTACCAGACAACAGA	51317
rs774194077	in-del	-/TTAAA	0.00013985	0.00836096	downstream-variant-500B, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928921	CGCCATCCCTGCTAT[-/TTAAA]TTATTTAAGGTCTCT	51317
rs774195293	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45942626	TTTAGAGAATGATGA[A/T]TCTGTAACCACCAGC	51317
rs774203517	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45960966	CTGCTTCCTTGAGAT[A/G]AAGCATATTACTGTG	51317
rs774203644	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45974252	CTTAGATCTTTACCC[C/T]TACTCTGGTGCTTCT	51317
rs774210709	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46029384	ATTCCCTTTGAGTTT[A/G]AGGATTAAAAAATTC	51317
rs774226367	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45935862	CCATGAGTCCTACAA[C/T]CCAGTGCAGAGAATC	51317
rs774243462	in-del	-/GAAA	1.64814e-05	0.00287061	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946046	GGAAAAACGGGGAGG[-/GAAA]GAGAGGGGGAAAATG	51317
rs774248266	snp	A/G			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46049449	AGTGTATTCCTGTAC[A/G]GTGGCATCTGCAAGC	51317
rs774252435	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46074122	GGTTTTGTCAGATGC[-/A]AAAAAAAAAAAAGTT	51317
rs774282339	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46012422	TATAGTCATTCCCTG[A/G]ATAACAACATTCAGT	51317
rs774285576	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46002699	CTGTCCCCGTAAAAT[A/G]TCCTATGTGTGCAAA	51317
rs774296574	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042338	GGAGCTAGAATTTGA[C/T]GGTAAACCAGAAGAT	51317
rs774297096	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45975808	CATTGCTTTCTCTAC[A/G]CCTTGGTATATGCCA	51317
rs774298482	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46027706	AGAGCTATGAGAAGA[C/T]GCCTATTGTTCCCAT	51317
rs774326426	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46106522	TAAACAAATACTAAA[C/T]AGAATAATTCAAGTT	51317
rs774327820	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46063987	ATAAATAAAATCACA[A/T]ACTCAGAAAAACAAA	51317
rs774329788	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46077789	CATGATCACCAACTA[C/T]AACAGAAATGATAGT	51317
rs774334752	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46068475	TTCGTTATTCACACT[A/G]CCTATCACTCAAAAA	51317
rs774340256	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45938547	TGGGGAATATGTTCC[A/C]AGACCCCTAGTGGAT	51317
rs774361034	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46051101	AGCTTTCTAAAAGCA[C/T]AGTTAGTCTCTCTGA	51317
rs774403837	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46015436	CAATTTCCAGAAAAG[-/T]ATTTCCAAGGTTTTC	51317
rs774422079	in-del	-/TATA			intron-variant	PHF21A	GRCh38.p7	11:46108568	AAATGTGTGTGTGTG[-/TATA]TATATATATATATAT	51317
rs774424587	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46083249	TGCAGCGGAACAAGA[C/G]TTTAACGAGATCCGG	51317
rs774433578	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46107673	CTTTTTATTACCTGT[G/T]TAACAAAATTTTTTA	51317
rs774462249	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45949459	TGTTCTTCTTTTTCG[C/T]TCTTGCCTCTTGCTT	51317
rs774470285	in-del	-/ATAG			intron-variant	PHF21A	GRCh38.p7	11:46078375	GATATAGATATAGAT[-/ATAG]ATAAAGATATATTTG	51317
rs774488270	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45970832	GAGACATAAATGAAA[C/T]AGTGTGTATGCCTCT	51317
rs774500468	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46083365	AGTAGTTACCAAAGG[C/T]CCAAGATATTCTCCC	51317
rs774542092	snp	A/G	1.68909e-05	0.00290606	intron-variant	PHF21A	GRCh38.p7	11:45938153	TTGGACCCACCCACA[A/G]TACCTGGTCCTGACA	51317
rs774560618	in-del	-/GT			intron-variant	PHF21A	GRCh38.p7	11:46010110	ATGCCAAGTTTGAGA[-/GT]GTTACTGCAGGAATG	51317
rs774583719	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45948425	AAGTTCTCAAGTGTG[A/G]CTACCTCTTTCCTTC	51317
rs774590351	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46116473	CATACTCACTAAAAT[C/T]AACTACTATCACATC	51317
rs774591081	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46025775	TTTCTCTGGAATTAT[C/T]TGCAAGTCATAGGCA	51317
rs774617781	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45965826	TAGCTTTTGATTCTA[A/T]ACCCTGAGCTCCCTC	51317
rs774644289	snp	C/T	1.75625e-05	0.00296327	intron-variant	PHF21A	GRCh38.p7	11:45971400	CAGATATTAGGACAC[C/T]AAATCTAAACTAAAT	51317
rs774658103	snp	A/G	1.64798e-05	0.00287047	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979810	ACTGCTGGGCGTGGT[A/G]GTGGTGGTACTGCTG	51317
rs774663874	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46072623	CTGAATGTCTAAATG[C/G]AATAACTATGAAGGA	51317
rs774682602	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45979118	GCCTCCTGGGTTCAA[C/G]TGATTCTCCTGCCTC	51317
rs774687097	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45954941	AAAAACACAAGCACA[C/T]AGATCTTTGATTTTC	51317
rs774692186	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45995561	ATAGAGTGGTTGAGC[A/C]GTTCATTTTTCTTTA	51317
rs774705195	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45940512	TTTAATGTTTCTTAG[C/T]AGGAAAATGTGACCA	51317
rs774711264	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46081404	TGAAAAAAGCTCTTG[A/C]TTTTCCTTTTTGATT	51317
rs774724787	snp	C/T	1.6477e-05	0.00287024	intron-variant	PHF21A	GRCh38.p7	11:45949362	AGCTCATAAATAAAA[C/T]TGGAACATGAGGGAA	51317
rs774734170	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46059833	CCAGATTCAAGCAAT[G/T]CTCCTGCCTCAGCCT	51317
rs774737096	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46032371	CACTGCATAGTGTGC[C/T]ACCATGTCCTTCGTT	51317
rs774752540	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46024941	CATCATCCCTTATTA[C/T]TGAACATCCCTTCCA	51317
rs774780204	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45993973	AGGGCTAGATAACTT[A/G]CTTCAAAGTGCCAGG	51317
rs774801648	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46115365	ACATTTTTACAAAAG[A/G]TAACTATTCAAAAAT	51317
rs774842816	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46038722	TGGCGAGGTGGCTAA[A/G]CATGCTAGCATACTT	51317
rs774865472	in-del	-/TT			intron-variant	PHF21A	GRCh38.p7	11:45988525	CTTAATATCACACTC[-/TT]GATGCTTAAAATCAT	51317
rs774871906	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45956545	ATTGCATGACGCTGA[C/G]ATTGGGGCTTCAACT	51317
rs774872293	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46007554	CCTGACCTCAGGTGA[C/T]TCGCCTGCTGTGGCC	51317
rs774880884	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46022834	ATTACCCAGGCTGGA[C/G]TGCAGTGGTGAGATC	51317
rs774882080	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46097534	AAAGAATACTAAAAT[A/G]AAGACTAAAACTATA	51317
rs774929532	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46061509	CAACATTTTGCTATT[C/T]CTGGAACTTAAAATT	51317
rs774940041	snp	C/T	1.65913e-05	0.00288017	intron-variant	PHF21A	GRCh38.p7	11:45936613	AGAAGGAGGTTTAAA[C/T]ACACATCCTCTATGT	51317
rs774952477	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46115103	TGAGATATTTTCACC[-/A]AAGTCTTTTTTATTT	51317
rs774957217	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45970837	ATAAATGAAACAGTG[A/T]GTATGCCTCTGTGAA	51317
rs774968066	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46096946	CTCAGTAAATGGTAA[C/T]TCCACCCCCTCAGAA	51317
rs774991493	in-del	-/AAAC			intron-variant	PHF21A	GRCh38.p7	11:45976836	CAGATCCTGTCTAAA[-/AAAC]AAACAAACAAACACC	51317
rs775032481	snp	C/G	1.66882e-05	0.00288857	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084264	TCTATAGTTTCTTCA[C/G]CCTCTGTTTAAAGTA	51317
rs775052708	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46009518	TGCACACATTTATTA[C/T]AGTACTTACTATAAG	51317
rs775071703	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45947779	AAATCACCAAGCACA[A/G]AACAAAACAAAACAA	51317
rs775077634	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46089986	GTGCTCAGCCCAATA[C/T]ACAGTTTCTACCTCT	51317
rs775085567	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45952578	TTTTTGTGACTAGTA[-/C]TTCTTTTTGGCTTAA	51317
rs775086242	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46097681	AGACTCACTGATTAA[C/T]AGAGATCTGCTCAAA	51317
rs775109076	snp	C/T	1.6552e-05	0.00287676	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965454	TGCCCATTGACGACA[C/T]GGACGGGGTGGATGG	51317
rs775116788	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46026607	ATTGAATGGCTGACT[A/G]TCTTTTATAATCTGA	51317
rs775134599	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46035842	AAAGAGAGGTTGGAG[-/A]AAGTAGGTATGTATC	51317
rs775144882	snp	A/G	1.651e-05	0.0028731	intron-variant	PHF21A	GRCh38.p7	11:46079189	TAAAGAGAGAAAAAG[A/G]GCCATCAGTCTTACA	51317
rs775148242	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46051646	CATGCCAATGTGCAA[-/T]TTCCATTCTGTAGTA	51317
rs775149496	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45955100	CACTGGTGTTCTCTC[C/G]TATTTCCCCCTTTAT	51317
rs775150412	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46102578	CCATGAGACTAGAGA[A/G]CAGTCTAATAAATTA	51317
rs775163342	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45964793	AATGTTTCAATATTT[A/G]AGCTAAAATATCTGC	51317
rs775210702	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46066560	ATAAATTAGCCAGGC[A/G]TGACAGTGCATGCCT	51317
rs775211122	snp	C/T			utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084244	TCTCCACTTTCTCTG[C/T]TAATTCTATAGTTTC	51317
rs775248660	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45988371	TTAGAAAAATATATC[A/G]TAGCAGGCAGTATAT	51317
rs775249373	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46007217	GGTTCTAAGAGATGA[G/T]AAAAGGGCCCCCTGT	51317
rs775303207	snp	C/T	1.75934e-05	0.00296587	intron-variant	PHF21A	GRCh38.p7	11:45946105	CCTCATTGGCTAGCA[C/T]GGAAAAGGAAGTGAG	51317
rs775305439	snp	A/G	0.000882131	0.020983	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965341	GACTTGGCTTGCTAA[A/G]CTGTACAGTTTGAGG	51317
rs775307659	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46038324	GTAGATACGGGGTTT[C/T]ACCATGTTGGCCAGG	51317
rs775314606	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45948945	ACTGCACTCTTCTTA[C/T]GCTTTGAGGGTTGAA	51317
rs775338999	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46016296	ATGTCATTTCATGAC[C/T]CAAAATTTCCCAGAG	51317
rs775368298	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46076505	GAGTTTAATTAACAC[A/G]GTTAACGGCAGCCTG	51317
rs775416874	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46050338	TTGAAGAAAAGTGGC[C/T]GGCTTACTTTGATCA	51317
rs775426868	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46014221	TCTTTATGTCCAAGT[A/G]TACCCAATGTTTAAC	51317
rs775448348	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45951044	GCTGGTCAAAATACT[A/G]GGCCCTGAAGATGGA	51317
rs775463772	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46103037	TGGGCAATCACCGGC[A/G]GCATCTCTACACAGG	51317
rs775482827	snp	G/T			synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935738	TTTCTCTTCTTCTTT[G/T]GCTAAAAAAAAAAAA	51317
rs775508814	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46065359	CCTTTTTTGCCCCAG[C/G]ATGTTGATGTGTGAA	51317
rs775517030	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46030665	TTTTAAACAACTGCA[A/T]CATAAACATAATAAA	51317
rs775565665	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46109306	GAGGATTAAAACTAA[A/C]TAAGATCCTATGTGT	51317
rs775570341	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46094617	GAAATCCTGGCCGTG[C/T]ACAGTGGCTCATGCC	51317
rs775587079	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46069472	TTGGCTGTGAACCAC[A/G]GAGGGTAACATTTTA	51317
rs775589872	snp	A/C			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46120919	AAGAGAGAATGGAAA[A/C]GCTGGGATACTGCAC	51317
rs775630715	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46119310	AACACAGCCACAAAG[C/T]TCACTGTCAAGGCCA	51317
rs775649506	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45996810	CAGAATAAAGTTTCC[A/G]TCATAGCAGTTTGTG	51317
rs775653706	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45967471	ACTCTCATAACTTGG[A/G]CACATCCATTGTGGG	51317
rs775677055	snp	C/G	1.80994e-05	0.00300822	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933921	AGTCTTCAGTGTTCT[C/G]TTCTCCTTGCCGCCG	51317
rs775698053	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46005808	AAACAATTTACTCTA[A/G]CTGTATGAATCTGAT	51317
rs775700917	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46116240	GTAGTCATTTCCTTG[G/T]GCATCCTTCTAAAAT	51317
rs775703789	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:45984599	AGGTTCGTTTTTCCA[-/C]CGTTTAAGTCACGTT	51317
rs775741369	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45966489	CACTAAAAACAGTGA[A/G]AAAAAGTTACAGTTA	51317
rs775745920	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45949907	CCAGAAAATATAAAG[C/G]CTTATCAGAAGAGCA	51317
rs775786830	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46054666	GAGAAAAATCATTAC[C/T]ATTCAAATCACTATA	51317
rs775789493	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46032497	TTTTTCAATTCTCCA[C/G]TATTATTTAAAAAAA	51317
rs775795263	snp	C/T	3.31279e-05	0.00406975	intron-variant	PHF21A	GRCh38.p7	11:45950283	GAAACAAAAGAAGAA[C/T]ATGCTTCAGTCTGGG	51317
rs775798190	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46004775	CTAAAGGACTCATCA[A/T]CTAAAAGATGTCTTT	51317
rs775815335	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46020200	TTTGTGGCATCAGTG[A/G]TGTCATTTCCTAATG	51317
rs775829609	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45980426	TGGTTAACAGTACCC[C/T]TGAGGTTCTTATGAG	51317
rs775855709	snp	C/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932492	GCCCACCAGTCTAGA[C/G]ACACACACACGGCAA	51317
rs775884838	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46068550	TACAGATATGTTCTA[C/T]GCAAAAGAAAAAAGA	51317
rs775891950	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46010826	CCCAGTGGACTGAGG[A/G]TAATAATGATCAGTT	51317
rs775902891	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46047218	TCCCTATGTAACTCA[C/T]AGGGGTGTAGGGAGG	51317
rs775903690	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46033579	CATTTTCTGTTATTA[C/T]TAACAAGGCTGCTAC	51317
rs775904868	snp	C/T	9.95818e-05	0.00705556	intron-variant	PHF21A	GRCh38.p7	11:45980001	AGAAATAAAAGATAT[C/T]AGAATACTGCTCTAT	51317
rs775934701	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46100674	CATGCACAACTTTCA[C/G]TGACTATGCTTCCCC	51317
rs775955831	snp	C/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084912	GTCTTGATCTCCTGA[C/T]CTCGTGATCCACCCA	51317
rs775961410	snp	A/G	1.69807e-05	0.00291377	intron-variant	PHF21A	GRCh38.p7	11:45938337	TGAGAGGAAAGGTAA[A/G]AAAAAGGACAAAAAA	51317
rs775967254	snp	C/T			synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979835	CTGCTGCTGTTGTTG[C/T]AGTTGCTGTAGTGGT	51317
rs775976012	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46018812	TAGGAGCAGATGGTG[A/G]TAACTCACTTAATGG	51317
rs776014983	in-del	-/CTT			cds-indel, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931521	AGCCTAACTTAATTC[-/CTT]CTTCTGAGGCCCCTG	51317
rs776020882	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45942073	AACATACAGAGACCT[C/G]TGTGTTGATTTTAAT	51317
rs776061193	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46102108	TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT	51317
rs776088482	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46050395	TTTCCCTGTTCTGCT[A/G]ACTGTGAGCATGTTG	51317
rs776103966	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45995934	GTATATGGCTTTTTT[A/T]AAAAAAATAATTTTT	51317
rs776108597	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45957167	GATTGAGGACAGAAA[C/T]AAACAGTTCTACAAT	51317
rs776111120	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45941246	TGGGACTACAAGTGC[A/G]TACCACCATGCCCGG	51317
rs776133497	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46098897	GTGAGAACCCTTTCT[A/G]TTGCACTAACTGTAA	51317
rs776142214	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46116527	AACTGTAATAGGGGA[C/T]ATACAATTCACAGGA	51317
rs776157376	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46061792	GAATTCCCTGTTTTC[A/G]GAACCAATGCCTTCA	51317
rs776161407	snp	A/G	1.85682e-05	0.00304693	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965565	ATGGGAGGTGGTGCT[A/G]GGGCAATAGGAATGT	51317
rs776193825	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997349	AATATCAGAAGTGTA[C/T]TTGCAAATAACAGGA	51317
rs776198718	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45972811	CCCAGCTACTCGGGA[C/G]GCTGAGGCAAGAGAA	51317
rs776217994	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45959090	ATTTATCCCAAGAGT[C/G]GAAGGGTGGTTCAAT	51317
rs776224637	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45973709	TGTAGTAAGTGTTTT[C/T]ACCACAGTGTATTAG	51317
rs776226456	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46099173	ACAAGATTAAAACAA[C/T]CAAATTTTAAAAAAT	51317
rs776231709	in-del	-/CT			intron-variant	PHF21A	GRCh38.p7	11:46039227	TTAAAAAGTTATCTC[-/CT]GTTTTCGTGCATTCG	51317
rs776242325	in-del	-/AAAAAAAAAA			intron-variant	PHF21A	GRCh38.p7	11:45968933	CGAAACTCCATTGCA[-/AAAAAAAAAA]AAAAAAAAAAAAAAA	51317
rs776246019	snp	C/T			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46075133	ATGTCTTAACATAGA[C/T]AGTTGCAATTTTCTA	51317
rs776249059	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46062561	ATCTAGGGATCTAAA[G/T]TTATAGTTATTTTGA	51317
rs776345024	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46054113	TTTCTTGAGGCTTCT[C/T]ACCCACCAAAATGTT	51317
rs776367492	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46116816	CAAAATACAAAACTT[A/T]GCCGGGCGTAGTGGC	51317
rs776410393	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45937329	ATAGTTGAGAAAAGG[C/T]GACCAGAAACCAAAG	51317
rs776435004	snp	A/G	1.69714e-05	0.00291298	intron-variant	PHF21A	GRCh38.p7	11:45934243	GCAGCAAATGACAAG[A/G]GCAGTGGCACTGAGC	51317
rs776435846	snp	A/G	0.00018558	0.00963098	intron-variant, missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935219	GAGCGAGGGAGGGCC[A/G]TACGGATGGGCCCAC	51317
rs776445564	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46026656	AAAATCCTTTAAAGT[C/T]AAGCAGTGGAATTAA	51317
rs776504336	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46092517	AAATGAAATGCACCT[A/C]ATTTAAATAACATAC	51317
rs776520620	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45935961	TACATAAATGAGATA[C/T]CACATCTCATTTTCT	51317
rs776535588	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46025413	TATCCCCTTTCTTCC[C/T]GCTTTAGCACCAATT	51317
rs776553641	snp	A/G	0.000281557	0.0118617	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965459	ATTGACGACACGGAC[A/G]GGGTGGATGGAATTC	51317
rs776576404	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46003732	AATTTTAATTTGAAA[A/G]GTACTGGCAAGGCCT	51317
rs776615441	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46091650	AATTAACCTAAGCCA[C/G]TCTGCACATATACTA	51317
rs776628737	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46042495	AATGGTTTTTATAAA[C/T]CCTAGAAAACCGAAG	51317
rs776648497	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46079555	AAACCGGCCTGTTCA[C/T]ACACAGAGCAAAGTA	51317
rs776673322	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46062679	TTTAAGATTGAAGCG[C/G]TAAGAATGTGGAGCA	51317
rs776699605	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46029474	GGGCAGATCACTTGA[G/T]ATCAGGAGTTCAAGA	51317
rs776704740	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46090178	GAGTAAGGTATGAGA[A/G]CATAGTGACAATGAG	51317
rs776710568	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46111471	ACATGGCAAGACTCC[A/G]TCTCAAATAAATAAA	51317
rs776710720	snp	A/G	9.88321e-05	0.00702896	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45949433	GCTCCACTGTAGACC[A/G]GATTTGCTGTTGTTC	51317
rs776766020	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45965179	ACGTGGATGAATTAT[C/T]GCACATAAGCGACAG	51317
rs776826224	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46094666	AGTGGGTGGATCACG[A/G]GATCAGGAGATCGAG	51317
rs776843007	snp	A/C	7.5543e-05	0.00614539	intron-variant	PHF21A	GRCh38.p7	11:45935744	TTCTTCTTTTGCTAA[A/C]AAAAAAAAAAAAAAA	51317
rs776848430	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45993777	AAATTGAAAGGGCCA[A/G]GCAGGAGAGGAGCCA	51317
rs776859587	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46011000	ACACACACACACCCC[-/T]TCTCAAAAAAGTGAT	51317
rs776882376	in-del	-/GACT			intron-variant	PHF21A	GRCh38.p7	11:45964503	TTCAGGATCACCACA[-/GACT]ATTTTCAGATAAATG	51317
rs776886739	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46108053	TAATTAAAATATTAC[A/C]TGTATTATCTTGGTT	51317
rs776896405	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45951202	AATAATACATTATCA[A/G]TTTATTTCTCTGATG	51317
rs776897485	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46108726	AATATTTCTTGAAAG[C/G]ACACTTATCTAACAC	51317
rs776898464	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45968761	ATGACAAAACCCCGT[A/C]TCTACTAAAAATACA	51317
rs776919731	snp	A/G	1.64808e-05	0.00287057	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971179	CCCAGTGACCTTACT[A/G]GACGTCTGGAGGTTG	51317
rs776928361	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46041618	CAGGTCCTACCCAAT[C/T]TGTTGCTTTATAAGC	51317
rs776936399	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45992581	CATCACAAGGTGAAC[C/G]AAAAATGATTTTAGA	51317
rs776940895	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46006142	ACCAGATTAACTGAC[A/C]AGTAGATCACTGTTG	51317
rs776951393	snp	A/C	1.66007e-05	0.00288098	intron-variant	PHF21A	GRCh38.p7	11:45950294	AGAATATGCTTCAGT[A/C]TGGGTTCTCACAAAG	51317
rs776993478	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46058159	CCCTACATTCTACTG[C/T]TGCCTTACCATGGGG	51317
rs777037515	snp	C/T	1.64814e-05	0.00287061	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935649	ACACTTATGGAATTG[C/T]TGAGCTGTTTCACCT	51317
rs777043591	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46035369	TGCTAATCTGTTTGT[A/T]CCTTGCCAGCATCAT	51317
rs777099713	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46056706	GAATCAGGATTTAGC[A/G]GCAGAAATACAATGT	51317
rs777117354	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46050120	ACTGAAAGGAAATGC[C/T]TCACGCCAAGTTTTA	51317
rs777118116	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46050124	AAAGGAAATGCTTCA[C/T]GCCAAGTTTTAGAAA	51317
rs777133506	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46049056	TGACAGCTTGTGTTA[C/T]TGACAACAGGGATGA	51317
rs777171351	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46069806	TGAGTTAAATGTTAA[A/G]TGTTCTAAGCTTCTT	51317
rs777222440	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46080025	AGAAGTCCTAAAGTA[C/T]CTGGGAATAAGCTAT	51317
rs777225582	snp	A/T	1.64738e-05	0.00286995	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971266	CACCATAGCAATGGT[A/T]GGTCTCTGGCCCACC	51317
rs777229345	snp	G/T	3.30218e-05	0.00406323	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946064	AGAGAGGGGGAAAAT[G/T]ATCTTACATACCTTT	51317
rs777233913	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46030268	GATTTCTTTAAAAGG[C/G]TGTCAAGACAATATA	51317
rs777239065	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45980789	TGTTAAACAAAGAAA[A/C]CTTGATCCCAGTAAT	51317
rs777252917	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46057106	ACTACAATTGAGAGG[-/T]TTTTTTTCCCCAAGT	51317
rs777256005	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46017872	ATTACTTTGCCTTTT[C/G]AACTCTGTAATCTCA	51317
rs777261539	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45942498	GGGACAATCTTTGGC[A/G]CTAGCAAACAAGATT	51317
rs777308126	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46067598	ATATTCCACCCCCCA[-/C]AAAAAAAAAAAAAAC	51317
rs777317540	snp	A/G	1.64741e-05	0.00286998	intron-variant	PHF21A	GRCh38.p7	11:45948872	GCAAGGGAGAGATAC[A/G]AAAAGGTCCTCACCT	51317
rs777339363	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46084021	ATGACTTTGTCGAGT[A/T]GTGGTAAAAGGCAAA	51317
rs777372549	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45976785	GTTTCAGTGAGCTGA[C/G]ATTGTGCCACTGCAC	51317
rs777398661	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46066081	TTCAAAAGAAAGGGA[A/T]ATAGTCTCATAAACA	51317
rs777432892	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45991961	TGATTACATTTTGCA[A/G]GACATGTAATAGGAT	51317
rs777435876	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46043148	GCCATTTGGGTCCTT[C/T]AGAGGTAAGAAATTC	51317
rs777446652	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45931586	GACACATTTTACTCT[A/G]AGAAGTGTCTCTTCT	51317
rs777482858	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46094534	TACAATAAACACTAG[C/T]GAAATATTTTTGGAA	51317
rs777490263	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46080603	TTCTTAAATCCACAT[C/T]GTAGTTTTCCAGTCC	51317
rs777495429	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46104591	CACCACGCATTTCAA[-/G]GGAGAAAAAAAACCT	51317
rs777544190	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45968220	CATCCCCAATTTATT[C/T]TCTGCACAGAGGCAA	51317
rs777574822	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46070768	CAAAATTTAAAACCA[A/G]AAGATAATTTATGGA	51317
rs777618934	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45963601	GTTTTAAAAATGAAC[-/T]TTGTACTATCTTTGT	51317
rs777630398	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46006876	ATCAACAGGTACTAA[C/T]AATATGTATTTTCAA	51317
rs777646564	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46044474	CCCATTTGGATTTCA[-/T]TATCTTATTTTCCAA	51317
rs777656655	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46074459	GTGGCTCTTTTGGCG[-/G]GGAGGGGGGAAGGCA	51317
rs777679058	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46099946	TTTTTTAAAAAATCT[C/T]TGTAGTCCAACATAT	51317
rs777731972	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46020403	GCTCTGACACTGTTC[A/G]ATGGGTCTTTGCGCA	51317
rs777751919	snp	C/T	1.65307e-05	0.0028749	intron-variant	PHF21A	GRCh38.p7	11:45936444	TACTGCCAGTATTTT[C/T]TTCAAACAAGGGGAA	51317
rs777786242	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46038128	TTTCTCTCTCTCTCT[-/C]TTTTTTTTTTTAAAT	51317
rs777786926	snp	A/G	1.88642e-05	0.00307111	downstream-variant-500B, utr-variant-3-prime, missense	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928851	CCGAGGCTGAGGCTG[A/G]GCCGGCGCTGCCCCT	51317
rs777834307	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45956030	TATATTTAAAGTGCT[A/G]AGCAAAAAAACCCCT	51317
rs777854272	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45984604	GTTTTTCCACCGTTT[-/A]AAGTCACGTTCCATG	51317
rs777863171	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46060988	GTTCATTTTTGTATA[C/T]GGTGTAAGGAAGGGC	51317
rs777865316	snp	C/T	1.74909e-05	0.00295722	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965522	GGTCAGCATGACGGG[C/T]CTCTGGATAAGCTGA	51317
rs777923033	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45971727	GTTCTTTGCTTGCTG[A/T]CAATTAATTTAAACT	51317
rs777931828	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45978314	CAAAAAAACAATAAC[-/A]AAAAAAACAAACAAA	51317
rs777936359	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45957996	TATTGAAAAACTGTA[C/T]GCCAACAAACTAGAC	51317
rs777958692	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46098810	AGGAAGTGCCTCCTA[C/T]TAACACTAATGGGAG	51317
rs777963341	snp	A/C	1.69706e-05	0.0029129	intron-variant	PHF21A	GRCh38.p7	11:45938147	CCCCTGTTGGACCCA[A/C]CCACAGTACCTGGTC	51317
rs778012953	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46026164	AATATCCAAAACTTC[A/G]TTATATTTGGCTTTA	51317
rs778014730	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46009106	CAGCCTCCTGAGTAG[C/G]TGGGATTACAGGCGT	51317
rs778022407	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45976095	CCTTATCTCCTCTCC[A/T]TCGTTTCGTGGATCA	51317
rs778032298	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45973168	ACATCAGCTCCTCAG[C/T]TGCACTAGCCACATT	51317
rs778057230	snp	A/G	1.64811e-05	0.00287059	missense, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979803	GCAGCTGACTGCTGG[A/G]CGTGGTGGTGGTGGT	51317
rs778062753	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46075543	ACATACTAACCGACT[C/G]TGTTTATATTTTTTC	51317
rs778065609	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46045728	TGTTCTCTAAAACAC[A/G]TAGGTTACTAGACTT	51317
rs778099867	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46043079	CTCCTTTCCATAAAA[G/T]ATACCTGAAATTTTA	51317
rs778100794	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46024831	GAAAGAAAGACTTAG[A/G]GACTTCTTTAAGAAT	51317
rs778109186	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46033753	TAAAATATAAACACC[A/G]GATTTCAAAGACTTA	51317
rs778126590	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45954210	CCATGTTGGTCAGGC[-/T]GGTCTTGAACTCCCG	51317
rs778144530	snp	C/G	1.75062e-05	0.00295852	intron-variant	PHF21A	GRCh38.p7	11:45934276	CCTGGTTTCTAACAG[C/G]CCTGGCAGCCCCTAA	51317
rs778154144	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46091253	AATTTTTTTAAAAAG[A/G]AGTAGTCTTGCACTA	51317
rs778156440	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45940917	ACATCAAGAAACAGA[A/C]GGCAGAAAGACAGAA	51317
rs778182013	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46010034	CAAAAATTTTGGGGA[A/T]GTCTGAGGAACATTC	51317
rs778189027	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45937490	TTTATTATTAGTATT[-/A]TTTTTTTGAGACAGA	51317
rs778204462	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45936886	AGCTAGAACCACCAA[C/T]ACAAAAGCTGCACAT	51317
rs778223353	in-del	-/GAGAA			intron-variant	PHF21A	GRCh38.p7	11:46104966	CTTGTCTCAATCCTT[-/GAGAA]GAGAAGAAAGGAGCA	51317
rs778240966	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46072617	TCACAACTGAATGTC[A/T]AAATGGAATAACTAT	51317
rs778241431	snp	A/G	1.64942e-05	0.00287173	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084205	AAGAGCCTCCTGTAG[A/G]GTCTGCAACTCCATC	51317
rs778243879	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46089572	AGAGCTTGGCAACCC[A/T]GATTTTCGAGGCGAA	51317
rs778246926	snp	A/G	1.65979e-05	0.00288074	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45965393	AGTAGCTATCACAAT[A/G]CTGGTGAGCTGGGCC	51317
rs778247891	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46010060	CATTCATTTAGTTGC[-/T]TAACCATATCATACT	51317
rs778268740	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46038202	CACAATCTCAGCTCA[C/T]TGCAACCTCTGCCTC	51317
rs778281323	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46002113	TCCAATTTACATAAG[C/T]AAATGCTTTCATTAA	51317
rs778301159	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46020580	GATGATCTAGAATAT[-/A]AAAATACTATCCTCT	51317
rs778304203	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45946406	ATTTATTTTTTGAGA[C/T]GGAATCTCGCTCTGT	51317
rs778309744	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45965768	GCATATAATCTTATA[C/T]AAGACTCATCAGCTC	51317
rs778321514	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45964048	ACTAAAAATACAAAA[A/T]TAGCCAGGCATGGTG	51317
rs778329803	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45948794	AGGATAGAGGAGTTA[C/G]GTCCTATAATGATGG	51317
rs778332274	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46105992	TTAATATTTGTATAC[C/T]AACATGTAATATACA	51317
rs778342462	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46067977	TTGCTTAAGCTGAGT[C/G]TTCAAAGGATACATA	51317
rs778384121	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45985252	ACGCTGAGGATGCAG[A/G]AAGGAGACAGGGCAG	51317
rs778410992	in-del	-/CTA	0.000431313	0.0146789	splice-acceptor-variant	PHF21A	GRCh38.p7	11:45935740	TCTCTTCTTCTTTTG[-/CTA]AAAAAAAAAAAAAAA	51317
rs778419675	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45947264	TTCTAGGGGCAAGGT[C/G]ATTGCTTCTAAGCTA	51317
rs778435828	snp	A/G	0.00018558	0.00963098	intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935103	CCACTTGGACAGGCC[A/G]GGCTGGGCAGTACTT	51317
rs778436245	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46072246	CTACCAGCAATAAAC[C/T]ACCTACATTTTCCAG	51317
rs778450598	in-del	-/AAA			intron-variant	PHF21A	GRCh38.p7	11:46074122	GGTTTTGTCAGATGC[-/AAA]AAAAAAAAAAGTTGT	51317
rs778471961	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46081808	TTTATGGAAAAAAGC[C/T]ATACTCATTCATTTA	51317
rs778478774	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46017032	CTGGAGTGCAGTGGC[A/G]TGATTTTGGCTCACT	51317
rs778490305	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46114564	TTGAAGCTTCGTCAA[C/T]ACAACATACTGTCCA	51317
rs778497261	snp	A/G			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935008	CACTCCAACAAGGGT[A/G]ACCTACTCAATGGAA	51317
rs778514162	snp	C/G/T	3.43049e-05	0.00414143	intron-variant	PHF21A	GRCh38.p7	11:45938124	TGTCTTTGTCCTCCT[C/G/T]GGCCCCTCCCCTGTT	51317
rs778542167	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45948897	TCACCTCTCTTCCGG[A/G]TCCCAGGGTGCATTG	51317
rs778571454	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45983125	TCAGCCATATGGCTA[A/G]AGCAAGGTGACGACC	51317
rs778578963	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46015758	TCAATATTACTGTCT[C/T]TTACCTCTATACCTT	51317
rs778579358	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45977401	CTCGGCCTCCCAAAG[C/T]GTTGGGATTACAGGC	51317
rs778587877	in-del	-/AAAAAAAAAAA			intron-variant	PHF21A	GRCh38.p7	11:45987668	CCCCGTCTCAAAAAA[-/AAAAAAAAAAA]AAAAAAAAAAGCACC	51317
rs778592901	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45997747	TTGGGCCATCTGTTT[A/G]TGTGTGCTGCTTGTC	51317
rs778594317	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46064502	TTCCTAAACTTGGGA[-/C]GTAAATCAACTTTGG	51317
rs778595905	snp	C/G	1.75653e-05	0.0029635	downstream-variant-500B, missense, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928835	AGCCCCAGAGCCCTG[C/G]CCGAGGCTGAGGCTG	51317
rs778600637	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:45964348	AACTAGCTTCTTGAA[G/T]GCAAGGTCTGCCGCA	51317
rs778612148	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46079486	GCATCCCTTTCAAAT[A/G]TTGTCAATGTCTAGA	51317
rs778633604	snp	C/T	1.65411e-05	0.00287581	utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:46084229	CTCCATCCTCTACCT[C/T]CTCCACTTTCTCTGC	51317
rs778634866	snp	C/T	3.2956e-05	0.00405918	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971299	AGAGGCAGGCATGGT[C/T]GCAGTTGCTGCTTTC	51317
rs778635544	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46051965	ATGTGTTTCAAACTA[C/T]TAGTAGAATTCCAAA	51317
rs778677045	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46019919	CAGGGTTCCTAATAA[G/T]CTTAATCATCATGTC	51317
rs778699732	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46017729	TGATTTTGTCCCTAA[A/G]AACTGTTCTTGATAA	51317
rs778708686	snp	A/G					GRCh38.p7	11:46123318	TTTTTTACTTTCGTG[A/G]CCTGCAAAATTAAGT	51317
rs778711141	snp	C/T					GRCh38.p7	11:45939320	AACAATTCTCATCAC[C/T]TATCAATTCTAGGGG	51317
rs778721027	snp	A/G					GRCh38.p7	11:46080944	GCTGAGATTACAGGC[A/G]TAAGCCACCATGCGC	51317
rs778743545	snp	C/G					GRCh38.p7	11:46044809	GAATATATTGCCTTA[C/G]CAAAACAAACATATA	51317
rs778806097	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46112791	ATATATCAGGCTTGA[C/T]AATAAGAGGCTTCTC	51317
rs778846604	in-del	-/C	0.000215458	0.010377	intron-variant	PHF21A	GRCh38.p7	11:46076738	AAAATATGCCCCCCT[-/C]CCCCTTTTCCCCTAC	51317
rs778858349	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45994646	TGGTTATGTTTTAGG[C/T]TTTGTAAGAACAAGA	51317
rs778859417	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46009553	GCACAGTTCTAAGCA[C/T]GCTATGTATTACATA	51317
rs778905073	snp	A/G	1.65012e-05	0.00287234	intron-variant	PHF21A	GRCh38.p7	11:45936472	GAAGCTTACAAAAAA[A/G]TGGGTATGGATAACT	51317
rs778920853	snp	A/C	1.65362e-05	0.00287538	intron-variant	PHF21A	GRCh38.p7	11:45950272	TCTGTGCCAGAGAAA[A/C]AAAAGAAGAATATGC	51317
rs778921693	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46098131	TCAGAGGGCAGATCC[A/G]TACCTTCATTTCATG	51317
rs778926438	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46006909	ATCTCAGAAAATGCA[A/T]AGTCAAAGTCAGAAC	51317
rs778942844	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46089911	GCCAGGCCAGGGTTC[C/T]CCATAGCACCCTCCT	51317
rs778946324	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45993657	TGGGGAGCTGGGCCA[A/G]CAGGGAGAGATGTCC	51317
rs778969425	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45998586	TGCGTGATCTTGGCT[C/T]GGCGCAACCTCCACC	51317
rs778970235	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45938082	AGACTGCCATTTCCC[C/G]GGGAAAGGAATTCCT	51317
rs778976872	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45952427	TGTTTATTTTTTGCA[C/G]AAACAAGGTCTCACT	51317
rs778977374	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46037343	TTCAGGCCTATTGAT[-/A]AAAAAATGGAGTGCT	51317
rs778984138	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45941929	AACACGGTACATCCA[A/G]AGGATTAGTGTCTGG	51317
rs779000670	snp	A/G	3.32132e-05	0.00407499	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945881	ACACAGGCTGAACAG[A/G]TGCAGGGAAAGTGAA	51317
rs779027357	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46046891	CACTGCTCCCCATGA[C/T]GAAAGTTTGAGTCAA	51317
rs779034128	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46007024	TTTTAATCTTTAGAG[C/T]GTTCCTGCAAGCTCG	51317
rs779062412	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45981599	CTCATATCTCATACA[C/T]TTTCAAGTTAGTTCA	51317
rs779066526	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46006203	TTTTAAAATTAAATG[C/T]TATAAACTTCATGCT	51317
rs779067518	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997732	TGTTCTGACTCATTG[C/T]TGGGCCATCTGTTTA	51317
rs779073402	in-del	-/CT			intron-variant	PHF21A	GRCh38.p7	11:46029515	CAACATGGTGAAACC[-/CT]GTCTCTACTAAAAAT	51317
rs779089673	in-del	-/G			intron-variant	PHF21A	GRCh38.p7	11:46117481	TGCAGGCTAACTTAA[-/G]TACATCAACCATATG	51317
rs779091320	snp	A/G			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084631	AATGAGACTATAACC[A/G]TCCAGGACACACTGT	51317
rs779123412	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46062312	CATTTTCTCTGTTCC[C/T]TTGTCTCAGAACTTT	51317
rs779127842	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46048364	TCCTTTTTATTGTCA[A/T]ATAATATTCTACTGT	51317
rs779142349	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46027134	CCCAGATTATAAATA[G/T]GCTGCCAATCCAAGC	51317
rs779148759	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46039755	AATTACAGATCACTA[C/T]CAGGATCTCAGTCAA	51317
rs779180143	snp	C/T	2.98583e-05	0.00386371	downstream-variant-500B, utr-variant-3-prime, synonymous-codon	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928903	CCAGGGCAACCTGCC[C/T]TCCGCCATCCCTGCT	51317
rs779224831	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46063090	TGACTCAATAAACCT[A/G]TAAGAGAGAAGTGGG	51317
rs779234033	in-del	-/TC			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45933836	CTGGCACAAGCATCT[-/TC]TCTCTCTCTCTGGAA	51317
rs779238900	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46073898	AAATCTCAAGTTACA[C/T]TTTAAAAGCACTAGA	51317
rs779247731	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46010621	ATTCATAATACTGCA[A/C]GTCAACAATCACAAA	51317
rs779255289	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45960134	GCAGTTCTTCAAATA[C/G]TTGAGCAGAATTACT	51317
rs779271386	in-del	-/TCTT			intron-variant	PHF21A	GRCh38.p7	11:46036024	GATTCAAAAAGAAAC[-/TCTT]TAAATAAGCCAGGCA	51317
rs779287493	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46089472	TTCTTATCATTTAGC[-/A]AATTTTCAACACATC	51317
rs779300647	in-del	-/AT			intron-variant	PHF21A	GRCh38.p7	11:46024013	GTAGCAACCTGTAAC[-/AT]ATGTGGGAACACTGA	51317
rs779307585	in-del	-/AGC			intron-variant	PHF21A	GRCh38.p7	11:45991263	TGAATGTATCACAGT[-/AGC]AGTACCTTGATTTTT	51317
rs779317310	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46075942	ACTGGCATGAAATAT[C/G]AACTGCAAATCACCT	51317
rs779340492	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45975776	TGTTCCCATTCCCTC[A/T]CCCAAAAAGAATTCC	51317
rs779343851	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46093405	TTATACCAAACATAC[A/G]ATAAAATTATTTAAA	51317
rs779355473	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46098841	TTCTGGGTGTAAACC[A/C]TAAGCACCAAGGAGG	51317
rs779384650	snp	A/G	4.96454e-05	0.00498199	synonymous-codon, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45938301	GCTGCAAAAATCCTC[A/G]TGAATATCACCCTAT	51317
rs779403187	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46092142	CTATCCAGCTAGCAT[C/G]AGGATCAGGCACACG	51317
rs779405279	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46074376	AAAATATCAGTCATA[C/T]GGATAAGGTAATTCA	51317
rs779418356	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46026435	ATCCTTTGCATAAAC[A/T]GGTGTCAAGGTTATT	51317
rs779438406	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45989323	AGAAGAAAAGCATGA[A/T]CGATCTCTTAATGAA	51317
rs779446175	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46115105	AGATATTTTCACCAA[A/G]GTCTTTTTTATTTAC	51317
rs779449360	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45990498	CTCCTGGACTCAAGC[A/G]ATCCACCCGCCTCAG	51317
rs779461972	snp	C/G			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932052	TCTCCCCAAAGGCAA[C/G]ACAGAGCGAAGGCCA	51317
rs779469699	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46092382	GAAAAAAAGAAGCAA[C/T]AGGTAATTTTTACAG	51317
rs779470618	snp	C/T	2.55679e-05	0.00357538	intron-variant	PHF21A	GRCh38.p7	11:45965642	ATAATTATTGTATTA[C/T]TTAAGCTGCTCAAGT	51317
rs779513275	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46074857	GAAAATAAGTCTGAG[G/T]ACGGATGAGCTTTTG	51317
rs779519473	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46109799	CCAGTCTACCCAACA[C/T]GGTGAAACCGTCTCT	51317
rs779522234	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46003573	TGATGACATTTTCAC[A/G]AAGGGCAGAGTGAGA	51317
rs779557079	snp	A/G	5.33338e-05	0.00516373	intron-variant	PHF21A	GRCh38.p7	11:45935570	CACACGTACTGTTAC[A/G]TATATTGGAAAGGCC	51317
rs779565374	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46093714	AATGCTCAATAAATG[C/T]TTGTTAAGTCAATGA	51317
rs779611033	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46107653	AAAAACTTTTATAAC[A/G]AAAACTTTTTATTAC	51317
rs779629794	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46003849	TTTCCTTTTTGAGTG[A/T]TGCAACCTAATATTC	51317
rs779683986	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46040613	AGTGCACCAAAAATA[A/G]CAGTATGTGCTGAAG	51317
rs779691312	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:45935354	GGCCATGGCTACACT[C/G]TTGTAGCTGTTACTT	51317
rs779720039	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46002383	CTTCAGAAATAAACT[A/G]ATTTGTAACTTTACT	51317
rs779732812	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46028604	TTTGAGACAGAGTCT[C/T]GTTCTGTCGCCCAGG	51317
rs779741877	in-del	-/GT			intron-variant	PHF21A	GRCh38.p7	11:46030830	TGTGCGTGTGTGTGC[-/GT]GTGTGTGTGTGTGTG	51317
rs779751750	snp	C/G	3.30743e-05	0.00406645	intron-variant	PHF21A	GRCh38.p7	11:45950187	AAAAAAAGGCAGTGC[C/G]AAGAATATCTTCTCT	51317
rs779766024	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46053960	AGAACCTGCTAAAAA[G/T]TGGCAGCATCCACGA	51317
rs779773972	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46039115	AGACAACTCTAAAGA[C/T]TTGACTTTTATTCTG	51317
rs779821360	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45966025	CTCCCTGTTCTTGGC[C/T]ACTCCTCCTCTCAGT	51317
rs779833383	in-del	-/TG			intron-variant	PHF21A	GRCh38.p7	11:46108555	AAACTTCTTTAAAAA[-/TG]TGTGTGTGTGTGTAT	51317
rs779839001	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45936380	CCAATAGTTAAGGGC[-/A]AAAGGTTTTCATTTT	51317
rs779853827	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46068125	ATGTATGAGAATGAG[A/T]TGCTAAAGGTATCAG	51317
rs779875024	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46045284	TATTTCTTTTTCCCT[A/G]TGAAAGATCATAAGC	51317
rs779884832	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46033196	TATGGTATTCCACCA[C/T]AGGAGTGTCCCATAA	51317
rs779901524	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46010132	GCAGGAATGAGAACA[A/C]TCATTTAAAGACAAA	51317
rs779924343	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46078547	GCCTAAGTGAAAAAT[A/G]CCTATGAGAATTTAA	51317
rs779951301	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45939948	TGCTGCTGTGGATTT[C/T]CTGGCTATTCTGCCA	51317
rs779951690	snp	C/G	1.64795e-05	0.00287045	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979778	TGAAGCAGTCAGGTT[C/G]GGAGAGGCTGCAGCT	51317
rs779958949	snp	A/G	3.31252e-05	0.00406958	missense, nc-transcript-variant	PHF21A	GRCh38.p7	11:45953544	GAGGGTTCTCCTCCC[A/G]TTTTGGTTTGGGTGC	51317
rs779977513	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46080986	CTATTCTAACAACCC[C/T]GAAACCCAGCTCAAA	51317
rs780038212	snp	A/C/T	0.000232127	0.0107712	downstream-variant-500B, synonymous-codon, missense, utr-variant-3-prime	PHF21A, LARGE2, GYLTL1B	GRCh38.p7	11:45928842	GAGCCCTGCCCGAGG[A/C/T]TGAGGCTGGGCCGGC	51317
rs780038776	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46111255	GGGCAGATCACTTGA[A/G]GCCAAGAGTTAAGAG	51317
rs780039605	snp	C/T	6.59011e-05	0.00573988	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979883	TAGTTTGTTTTCAGA[C/T]TGTGGCAATGGCTGT	51317
rs780046912	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46078037	CTGCCTCAGCCTCCT[A/G]AGTAGCTGGCCTTAC	51317
rs780071526	snp	C/T	1.76434e-05	0.00297008	intron-variant	PHF21A	GRCh38.p7	11:46076890	GTAGCAGGAAGACTA[C/T]GCATACTGCATTACA	51317
rs780101552	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978611	TGTAAGAGGTATCCA[C/T]GCTTAGGTTTCAGAG	51317
rs780103506	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45996482	CATCCTTGACAGTGG[C/T]CACATAAATGATTTC	51317
rs780121322	in-del	-/AAATGAAGACAA	1.65042e-05	0.0028726	intron-variant	PHF21A	GRCh38.p7	11:45979972	CTACTCTTTTCTACC[-/AAATGAAGACAA]AAAGAAATAAAAGAT	51317
rs780126198	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45985068	TCAGACACACCAATT[A/G]CTCAAAATGAAACCA	51317
rs780150629	snp	C/T	6.59446e-05	0.00574177	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45971319	TTGCTGCTTTCAAGA[C/T]GAGAGGTAGTGTCTT	51317
rs780157516	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46058070	CTCAACTTTTAACAA[A/C]GCCTTGTTAAATGTG	51317
rs780192879	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45994976	TAACTCCATCTTGAG[A/C]CCACAGAAATGTGTA	51317
rs780196213	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46034665	GTGGCTATCTATGGC[C/T]GTGCTACTCGCCTCC	51317
rs780218963	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45950761	AAAATCCTCTTAAAA[A/G]GAAGAGGATTTCATA	51317
rs780253152	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46115749	ATTAAAGGTCAGAGA[A/C]CTAAAACTTTAATTC	51317
rs780253626	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46036015	AAGCAAGAAGATTCA[A/G]AAAGAAACTCTTTAA	51317
rs780270638	snp	C/T	1.65201e-05	0.00287398	intron-variant	PHF21A	GRCh38.p7	11:46076730	ACAACGTTAAAAATA[C/T]GCCCCCCTCCCCTTT	51317
rs780273754	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46013281	TTTTAAACTGCACGC[C/T]TAGAGTAGCCTGACG	51317
rs780274403	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46050012	TGTAGTCACCACATG[C/T]TCAATTTGCTGTAGG	51317
rs780333766	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45975312	CAGTGAGACCCTGTC[C/T]CAAAGAAAACAAAAT	51317
rs780344547	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46070880	ATACATCTTCCAAAT[G/T]AGCAGAGTGCTTTTT	51317
rs780346786	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46088778	ATAGAACTTCTCTAC[A/G]TAGTATATATCTAGA	51317
rs780374392	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46029444	TGTAATCCTAATACA[-/C]GGGGAGGCCAAGGCG	51317
rs780374414	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45985913	ATAGTACAAATAAAC[A/C]AATTGACAACAGCAG	51317
rs780379759	snp	A/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46085484	TTCTTTTCTTGAATG[A/T]GGCCTTAGACATGAT	51317
rs780389428	in-del	-/TT			intron-variant	PHF21A	GRCh38.p7	11:46112910	GTTTTCAATATATTA[-/TT]TTGTGTGTAAACCTT	51317
rs780397923	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:45958449	TATATATATATATAT[-/AC]ACACACACACACACA	51317
rs780423906	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45969365	TTTAGAAGCAAGGCT[C/T]TGCCTTTAAGCATGA	51317
rs780428688	snp	C/T	3.54925e-05	0.00421248	intron-variant	PHF21A	GRCh38.p7	11:45969776	TGAGGATTTCTGTCC[C/T]ATCTAACCTATCATT	51317
rs780436644	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46087142	CTTCTTTTTGGGGTA[C/T]TGATATTTTCAAAAT	51317
rs780464054	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:45997936	AAAAAAGTGATACAC[A/C]ACAGGCCCATGTGCA	51317
rs780471778	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46005800	CAATTCTGAAACAAT[C/T]TACTCTAGCTGTATG	51317
rs780474268	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46089212	TTGACAGTCATCTAC[A/G]TATCTTTACTTCTTG	51317
rs780499969	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45943567	ATAGGCCCTTTTCTT[C/T]TGCATATTTTAGACA	51317
rs780512254	in-del	-/AA			intron-variant	PHF21A	GRCh38.p7	11:46118419	AAAAGTCTGATGTTA[-/AA]AAAAAAAAAAAAAAA	51317
rs780516520	snp	C/T	1.65534e-05	0.00287688	missense, intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45945910	AATGTGGTCTCTGTC[C/T]TTTCATTTTCAGGGG	51317
rs780540438	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46062418	TCTTCCATCTATTTA[C/T]TGAGAAACAACTCCA	51317
rs780550168	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46011970	CTCTATCTAGATTTC[C/T]AGATGACTATCACCT	51317
rs780563949	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45987569	GGGAGGCTGAGGCAG[A/G]AGAATTGCTTTAACC	51317
rs780584044	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46021733	TATTTTATTTTTTTG[C/T]AGAGATGAGATCCCA	51317
rs780589698	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45960353	CATGTCATGGAATAT[A/T]ATTCAGCCATTTAAA	51317
rs780597546	snp	A/G	0.000371058	0.0136158	intron-variant, synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45935223	GAGGGAGGGCCGTAC[A/G]GATGGGCCCACTCGC	51317
rs780609372	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46116486	ATCAACTACTATCAC[A/G]TCACATCAATGGAGA	51317
rs780610883	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46077466	AAAGTAGGCAAAAAA[C/T]TCCAAAATTAAAGTT	51317
rs780613105	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46077213	ACACACTACATGCTT[C/T]ACAGCATTATCAACA	51317
rs780614009	snp	C/T			intron-variant, utr-variant-5-prime	PHF21A	GRCh38.p7	11:46117942	ATCTTTCTGGAACTT[C/T]AAGGTGTTAATCCTG	51317
rs780614548	snp	A/G	1.71602e-05	0.00292913	missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45934017	GTGCAGCTCTGGGAG[A/G]AGGGGGAAGGGGCCG	51317
rs780641317	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46042216	TTGGGGCCTGTGGGA[A/T]AGCCACATGACAAAA	51317
rs780646685	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46104943	AAGCTCAGGCTCTTA[C/T]ACTAATACTTGTCTC	51317
rs780671901	in-del	-/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	PHF21A	GRCh38.p7	11:45932676	ATTTAAGTAACACTA[-/G]GAAGACCTCAATATC	51317
rs780672781	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45991654	CTGTAAAAATAATAC[A/G]CTGGGTCGAGAAACC	51317
rs780675818	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45958882	GCAATTGTACCACTA[C/T]ACTCCAGTCTGGGTA	51317
rs780689025	in-del	-/TC			intron-variant	PHF21A	GRCh38.p7	11:46089016	TCATCAACCAACATT[-/TC]TTTAACTAACGATAA	51317
rs780707606	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46079355	CCTTTAATAAAAAAA[C/T]CAAACCACCACTTTA	51317
rs780736986	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46027235	CTACAAGTTTTCTCC[A/G]TGCTAACAGGTACAA	51317
rs780781263	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45991823	TGTATATCTTTACCT[C/T]TATAGCACTGCACAG	51317
rs780826635	in-del	-/AAGTA			intron-variant	PHF21A	GRCh38.p7	11:46118705	ACCGATTCCATAAAC[-/AAGTA]AAGACAGAAGAAGAG	51317
rs780839518	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46040333	TACAGTGATGACACT[A/G]CTGGTAGTTATAAAC	51317
rs780886526	snp	G/T	1.73634e-05	0.00294642	intron-variant	PHF21A	GRCh38.p7	11:45935578	CTGTTACGTATATTG[G/T]AAAGGCCTAGGTCTC	51317
rs780919922	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46040931	CACACACACACACAC[A/G]CACGCACGCACAATT	51317
rs780955827	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46088526	TATCTGGAAAGCACA[-/T]TCACCATCCCAAAAA	51317
rs780960207	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45981091	TATACTCTGCACTTA[C/T]AACTATATTGCTGGC	51317
rs780990489	in-del	-/T			intron-variant, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46084682	CAACAGAATCATAAT[-/T]TTTTTTTTTTTTTTT	51317
rs781007896	snp	C/G			intron-variant	PHF21A	GRCh38.p7	11:46055428	GATGGGAAAAGTGTA[C/G]AGTACACAGTAACCC	51317
rs781042097	in-del	-/GAT			intron-variant	PHF21A	GRCh38.p7	11:46062052	AGAAGTCTGATGACA[-/GAT]TCTGATTCCCAATCC	51317
rs781051933	snp	C/T			utr-variant-3-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45929965	AGAGCAAAGTTGCCT[C/T]CACTCAACAGAAGCC	51317
rs781064263	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45950449	CTTGGCTTCCTTCAA[C/T]GTGGGCCACATTGGA	51317
rs781082525	snp	G/T	1.64863e-05	0.00287104	synonymous-codon, nc-transcript-variant	PHF21A	GRCh38.p7	11:45950222	TTCTAGATGGTCATG[G/T]GTTACCAACCCTAGA	51317
rs781086607	in-del	-/GTGA			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45935005	TTCACTCCAACAAGG[-/GTGA]GTGACCTACTCAATG	51317
rs781092948	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46114525	TACATTTCACCATAA[A/C]AGTGACGGGCTACTA	51317
rs781095484	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45960552	GCAAAAGTTAAATAA[-/T]TGCTTAATGGATACT	51317
rs781123066	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46068408	GCACATTATTTGAAA[A/G]CACATGATATAGTAG	51317
rs781140277	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46100536	TAATTTTTAAAATAT[A/G]TATCTTTGGTGTAGA	51317
rs781158015	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46107535	ATTCTACCAGGTCCA[A/G]TTCTTAGAATTTTAC	51317
rs781182355	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:45955923	GTAGCACAGCCTTAA[A/T]ATTACTGCAGCTCTA	51317
rs781223912	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46039952	TTAAAAACCCTCAAA[G/T]GAGTTTATTCTTATT	51317
rs781233674	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46031913	ATTATCAGGTACAAG[A/G]AACTGGATTGGATTG	51317
rs781245313	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45979698	ACAGGACCCAGTTCT[A/G]TATGACCAACAACAA	51317
rs781257945	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45938727	ATGGGAATGAGGTCT[A/G]TCTTCTTTTTTCTTT	51317
rs781272372	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45954378	ACATCTCACATACAC[A/G]GTCTCCTATTTCGGA	51317
rs781273810	snp	A/G	0.000567783	0.0168395	intron-variant	PHF21A	GRCh38.p7	11:46084145	AACAACAGTGTGGGA[A/G]AAGCCAATAATACAA	51317
rs781277394	snp	C/T	1.64757e-05	0.00287012	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979913	TATTTGGAACTTGTC[C/T]GGTTGTTCTTGCTTT	51317
rs781307421	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46033303	ACAGTCTTACTCTGT[G/T]GCCTAGATTGGAGTG	51317
rs781323165	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45985102	ATACTAAATTTTACG[C/T]GTATGGAAAAACTAA	51317
rs781324104	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46008804	CTGCAAAATGCTATG[G/T]TTGCAACTGTAAAAT	51317
rs781350738	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45971525	TCTTTTGTGTACATA[C/T]AGCATACTCCTTACT	51317
rs781412413	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:45991559	GCAGTAAGCTTATAC[-/AC]ACACACACACACATG	51317
rs781414309	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46024790	GGGTGACCAAGTGAG[A/C]CTCCATCTCAAAAAA	51317
rs781430528	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46097596	TATGCTCTTCCTTAT[A/G]ACAAGAATAATACCT	51317
rs781450296	in-del	-/CTCT			intron-variant	PHF21A	GRCh38.p7	11:45982374	TTCTGCTAGCACTGC[-/CTCT]CTGAGTAAATATTTT	51317
rs781459980	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46104048	CTTATGACAATTAAA[C/T]ATAGAAAGAAAATAA	51317
rs781489702	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46105749	CCAAATTTTACATTT[-/A]AAAAAGCACTAGGCC	51317
rs781512705	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46051337	GCATGTCATTTCAGT[G/T]CTGCCTGGGGGCCCA	51317
rs781514492	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46025544	CCTTTACCTGAGAAG[-/A]AAAATGATTCTCTGG	51317
rs781515260	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45936186	GGGAGGCTGAGGTAG[A/G]AGGATCGACTGGGCC	51317
rs781543906	snp	A/G	1.64833e-05	0.00287078	intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946050	AAACGGGGAGGGAAA[A/G]AGAGGGGGAAAATGA	51317
rs781557312	in-del	-/TGT	1.64852e-05	0.00287094	cds-indel, utr-variant-5-prime, nc-transcript-variant	PHF21A	GRCh38.p7	11:45979826	TGGTGGTACTGCTGC[-/TGT]TGTTGTTGTAGTTGC	51317
rs781558985	snp	C/G	3.29495e-05	0.00405877	intron-variant	PHF21A	GRCh38.p7	11:45948855	AAGCAAAAGCAACAG[C/G]AGCAAGGGAGAGATA	51317
rs781612038	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45978589	ACAGTGAAGACCTGG[C/T]GTTGGTTGTAAGAGG	51317
rs781656462	in-del	-/AGAAGGGAAC			intron-variant, nc-transcript-variant	PHF21A	GRCh38.p7	11:45946016	GACCTATATACCAAG[-/AGAAGGGAAC]AAAAGGGAAAAACGG	51317
rs781661877	snp	C/T	1.91254e-05	0.0030923	intron-variant	PHF21A	GRCh38.p7	11:46079104	TATTTTTAAATTTAA[C/T]AATTAAATGAATAAC	51317
rs781662340	snp	C/T			upstream-variant-2KB	PHF21A, LOC105376661	GRCh38.p7	11:46122827	AGCTTAACGTTTTTG[C/T]ATGGATGTATTACCG	51317
rs781691014	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46034242	CCCTTGCATACTTTT[C/T]CCTTGGGAGGCTCAT	51317
rs781708736	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45961607	TCCCCACAGAACCTT[A/G]GGATTTTTTTCAGTA	51317
rs781714946	snp	G/T			intron-variant	PHF21A	GRCh38.p7	11:46102202	GATACACCAGCCTCG[G/T]CCTCCCACAGTGCTG	51317
rs796090203	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45968065	TAATACCTATTTGCA[C/T]AGGGTTGTTGTAACA	51317
rs796110725	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46075812	ATAGAAACACAATAA[A/C]AAATCTCCAGAAATG	51317
rs796113519	in-del	-/AAAAAAAAAAAAAA			intron-variant	PHF21A	GRCh38.p7	11:45935742	TCTTCTTCTTTTGCT[-/AAAAAAAAAAAAAA]AAAAAAAAAGGAACG	51317
rs796117787	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46113843	AAAAAAAAAAAAAAA[-/A]GTTTAATTGTTTTAA	51317
rs796120212	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46105386	GGCACACAGGACATG[-/C]CCCTGATGATTAGAT	51317
rs796145239	in-del	-/ACAC			intron-variant	PHF21A	GRCh38.p7	11:46040931	CACACACACACACAC[-/ACAC]GCACGCACAATTAAG	51317
rs796156441	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:45998842	GTTTTTGTTTTTTTT[-/T]GAGACAGTCTCACTC	51317
rs796201216	in-del	AA/TTATGATTTT			intron-variant	PHF21A	GRCh38.p7	11:45940659	CTTCCTTCATTATTA[AA/TTATGATTTT]ATCAGGCTGAGGGCT	51317
rs796258958	multinucleotide-polymorphism	ATC/TCT			intron-variant	PHF21A	GRCh38.p7	11:45962687	CCTGAGGTCAGGAGT[ATC/TCT]AGACCAGCCTGGCCA	51317
rs796262576	snp	A/T			intron-variant	PHF21A	GRCh38.p7	11:46056169	TTTGAATTTCATCTT[A/T]TAAGGAGAAAACAGA	51317
rs796287390	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46056975	AGATAACTGATTTTA[C/T]TTGCTTTAAATATAG	51317
rs796333792	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45997492	GATGAAGCCAGCCCA[C/T]GCCTACGTGAAACAG	51317
rs796368678	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46094792	GTAATCTCAGCTACT[C/T]GGGAGGCTGTGACAG	51317
rs796369561	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46072005	TCTGTGTTAATATTC[C/T]ATGTTAAATATTATA	51317
rs796424142	in-del	-/AAAAA			intron-variant	PHF21A	GRCh38.p7	11:45957752	AACTAAATTCAAAGC[-/AAAAA]AAAAAAAAAAAAAGA	51317
rs796470316	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45983980	CTGCTGGTCACTGAC[A/G]AAGGTTATACTGGCA	51317
rs796511402	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:46092109	CAAAAAAAAAAAAAA[-/A]TCACAATATTTGAAT	51317
rs796525216	multinucleotide-polymorphism	CA/TG			intron-variant	PHF21A	GRCh38.p7	11:45962657	GCACTTTGGGAGGCC[CA/TG]GGCAGGTGGGTCGCC	51317
rs796537451	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46057269	AACTCAGCTATAATC[C/T]TTGCATGTCTATAAG	51317
rs796541998	in-del	-/TA			splice-acceptor-variant	PHF21A	GRCh38.p7	11:45935741	CTCTTCTTCTTTTGC[-/TA]AAAAAAAAAAAAAAA	51317
rs796635442	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	PHF21A	GRCh38.p7	11:46118787	TAAAAATGTAGTAAC[A/G]GTTTCCAACAATGCT	51317
rs796636730	in-del	-/AAAAAAAAAAA			intron-variant	PHF21A	GRCh38.p7	11:45981409	AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]CTATATTGCTCAGTA	51317
rs796663244	in-del	AGGATCAC/TGGGTCGCCT			intron-variant	PHF21A	GRCh38.p7	11:45962666	GAGGCCAAGGCAGGT[AGGATCAC/TGGGTCGCCT]AGGTCAGGAGTCTGA	51317
rs796695122	in-del	-/AC			intron-variant	PHF21A	GRCh38.p7	11:45955308	cacacacacacacac[-/AC]TTTTTAATCAAAAAG	51317
rs796702985	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46106820	GGCAGGCAGCCCTTT[A/C]CCTTTTGGTCAACTC	51317
rs796763448	in-del	-/AAAAAAAAAAAAA			intron-variant	PHF21A	GRCh38.p7	11:45968932	GCGAAACTCCATTGC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAATA	51317
rs796825130	in-del	-/C			intron-variant	PHF21A	GRCh38.p7	11:46091840	ctataggcacacacc[-/C]actgggcctggcTGG	51317
rs796825731	in-del	-/TTTC			intron-variant	PHF21A	GRCh38.p7	11:45971882	AAAGGACAGTGTCTT[-/TTTC]TTTCTTTCTTTTTTT	51317
rs796850119	in-del	-/GA			intron-variant	PHF21A	GRCh38.p7	11:46074461	TGGCTCTTTTGGCGG[-/GA]GGGGGGAAGGCATAT	51317
rs796892141	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45981422	AAAAAAAAAAAAACT[A/G]TATTGCTCAGTAAAT	51317
rs796896102	in-del	-/A			intron-variant	PHF21A	GRCh38.p7	11:45970023	ACAAGCTTTCATCGT[-/A]AGTTAATCATCTGAA	51317
rs796901322	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46049966	GTGATTAACTCAATC[A/G]AAGTAGGACCATATT	51317
rs796904074	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:46086408	ACAGGCATGAGCCAC[C/T]GCACCCAGCCAGCTA	51317
rs796915756	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:46071949	GCAGAGCAAAAGATC[A/G]GGTGGATAAAATAAT	51317
rs796953961	snp	A/C			intron-variant	PHF21A	GRCh38.p7	11:46059697	AAAGTGCTAGGATGA[A/C]AGGCATAAGCCATTG	51317
rs796966436	snp	A/G			intron-variant	PHF21A	GRCh38.p7	11:45944960	TAGAGACCAGGTTTC[A/G]CCATGTTGGCCAGGC	51317
rs796974742	snp	C/T			intron-variant	PHF21A	GRCh38.p7	11:45957946	AAACTGAGGACATTA[C/T]ATCTCACAGAATTCA	51317
rs796991359	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46049857	TCCTAAAAACAACGT[-/T]AAGACTATCCAGCAA	51317
rs796991509	snp	C/T			intron-variant, downstream-variant-500B	PHF21A	GRCh38.p7	11:45934725	GAGACGACAGGCCAG[C/T]AGCATTTAGGAGGAT	51317
rs796996763	in-del	-/T			intron-variant	PHF21A	GRCh38.p7	11:46016971	AATGTTTAACCTGGA[-/T]TTTTTTTTTTTTTAA	51317
rs797004993	in-del	-/ATTATT			intron-variant	PHF21A	GRCh38.p7	11:45974449	ATTATTATTATTATT[-/ATTATT]GCTGTTTATTTATTT	51317

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