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

PHF2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1963	snp	A/G	0.0759472	0.179459	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93670315	GGCCAGGTTTGAGCC[A/G]CAGGGAAGTGGGCAG	5253
rs8690	snp	C/T	0.139225	0.224118	utr-variant-3-prime	PHF2	GRCh38.p7	9:93679468	TCTAACAAAGTTTAT[C/T]GTGGCTATTAAAGTG	5253
rs914417	snp	G/T	0.301932	0.244547	intron-variant	PHF2	GRCh38.p7	9:93597513	GGGCCCTGGAATCAG[G/T]CAGGCTGTGGGGCAG	5253
rs928368	snp	A/G	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93610202	aggagaagaaaaaga[A/G]aaaggaatagaggat	5253
rs928369	snp	C/T	0.29046	0.246704	intron-variant	PHF2	GRCh38.p7	9:93586007	ACTGATTTAGGGGTT[C/T]AGGCCCATTTCCCTG	5253
rs951447	snp	C/G	0	0	upstream-variant-2KB	PHF2	GRCh38.p7	9:93575816	TGGGGCTGAGCATCA[C/G]GGAAGTCCGCGGGAT	5253
rs1000850	snp	A/G	0.493247	0.0577133	intron-variant	PHF2	GRCh38.p7	9:93585436	AGGGACAGCAAGCAC[A/G]GTTATGGAGCAGTGC	5253
rs1000851	snp	C/G	0.493201	0.0579089	intron-variant	PHF2	GRCh38.p7	9:93585467	CAGCCGCTCTGTGTG[C/G]GCAGCACGTGGCCTC	5253
rs1000852	snp	A/G	0.497613	0.0344622	intron-variant	PHF2	GRCh38.p7	9:93585608	TTGGACAAACATGAG[A/G]ATCTGATTGGCCTTG	5253
rs1041500	snp	A/G	0.498459	0.0277128	intron-variant	PHF2	GRCh38.p7	9:93590029	GCTATCCTGGTCTGT[A/G]TGTTTTTGTGCATGT	5253
rs1123475	snp	A/G	0.0520825	0.152737	intron-variant	PHF2	GRCh38.p7	9:93622669	gtctcaccgggctaa[A/G]atcaaggtgtgggca	5253
rs1132003	snp	C/T	0.168785	0.236441	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678446	TCTTGCCCTGCTGGC[C/T]ACACTCTGGAGAAGC	5253
rs1132004	snp	A/C	0.384401	0.210799	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678526	GGGCAGGGACAGTGG[A/C]CAGGCGGCCCGAGGA	5253
rs1132027	snp	C/T	0.0771285	0.180597	utr-variant-3-prime	PHF2	GRCh38.p7	9:93679273	GCAGTCCCTAGGGCC[C/T]GAGACTGGGTGGGAG	5253
rs1140722	snp	A/G	0.384785	0.210554	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678046	AGACAGAGTGAGCCA[A/G]TGCTCACCAGCCCCA	5253
rs1317260	snp	C/T	0.290977	0.246619	intron-variant	PHF2	GRCh38.p7	9:93592338	CACTCAGGGCGGGCC[C/T]ATTCTTTACTCATTT	5253
rs1412048	snp	C/T	0.421368	0.182025	intron-variant	PHF2	GRCh38.p7	9:93600685	GCCACAGCATGGAGC[C/T]TGTGTTACCATTTAC	5253
rs1412049	snp	A/T	0.349671	0.229272	intron-variant	PHF2	GRCh38.p7	9:93600641	ATGCCAGGGCCACCA[A/T]CCCACAACCTGCGAG	5253
rs1806458	snp	A/G	0.49645	0.0419827	intron-variant	PHF2	GRCh38.p7	9:93634049	CACTCGGTGTTCCTC[A/G]CAGGTGGTGACCTAA	5253
rs1806524	snp	A/C	0.34437	0.231505	intron-variant	PHF2	GRCh38.p7	9:93622242	GGCCTTGACCAGACC[A/C]CAAGCCCAAACTGAA	5253
rs1806673	snp	G/T	0.067446	0.170804	intron-variant	PHF2	GRCh38.p7	9:93631908	GCCCCTGGCCCAGGG[G/T]TTTCTGACACTTTCT	5253
rs1810886	snp	C/G	0.308123	0.244277	intron-variant	PHF2	GRCh38.p7	9:93596912	TACAGGCACGCGCCA[C/G]CACGCCCAGCTAATT	5253
rs1901280	snp	A/G					GRCh38.p7	9:93624941	gatgTCACTCTCAAA[A/G]GGGCAAGTTCTTTTT	5253
rs2001315	snp	C/T	0.45235	0.146814	intron-variant	PHF2	GRCh38.p7	9:93632120	AGGGTCTGGGTGAGG[C/T]AGGCACACAGGGCTC	5253
rs2001316	snp	G/T	0.20111	0.245173	intron-variant	PHF2	GRCh38.p7	9:93632064	GATGTCTGGGGACAT[G/T]AGAGAAATCAAAACA	5253
rs2001368	snp	C/T	0.237593	0.249692	intron-variant	PHF2	GRCh38.p7	9:93621740	AAAGTAGGCTTGTGC[C/T]GTCTGCCCCCAGGAT	5253
rs2001587	snp	C/T	0.0341408	0.126114	intron-variant	PHF2	GRCh38.p7	9:93633734	CACTGAGGCCAGGGG[C/T]CCCCGGCTACACCTG	5253
rs2001588	snp	A/C	0.0341408	0.126114	intron-variant	PHF2	GRCh38.p7	9:93633555	CCTATCCCAGAGCCA[A/C]ATGCGGAGCATGAGG	5253
rs2001589	snp	C/T	0.451856	0.147493	intron-variant	PHF2	GRCh38.p7	9:93633519	GCCCCTGTGACAACA[C/T]ACCCACTGAGACAAC	5253
rs2001609	snp	C/T	0.108402	0.206034	intron-variant	PHF2	GRCh38.p7	9:93633081	GCCTTGAACCTGCCT[C/T]CACCTGTCCTGCTCC	5253
rs2001610	snp	C/T	0.426507	0.177046	intron-variant	PHF2	GRCh38.p7	9:93633147	TCAGGGTTCCCAGAG[C/T]GAGCTGTGCCTGAGG	5253
rs2001994	snp	A/T	0.495782	0.0457324	intron-variant	PHF2	GRCh38.p7	9:93631567	TAAAGGGTAGGAAGG[A/T]TCAGCCCAGCGGGGC	5253
rs2001995	snp	C/T	0.190205	0.242744	intron-variant	PHF2	GRCh38.p7	9:93631645	GCCAAGCTGTCTTTA[C/T]GACAGGAATGACACA	5253
rs2026942	snp	A/C	0.498369	0.0285077	intron-variant	PHF2	GRCh38.p7	9:93588593	GCACTCCCTGCCCCC[A/C]AGAAAAACACTTTAT	5253
rs2150751	snp	A/G	0.290977	0.246619	intron-variant	PHF2	GRCh38.p7	9:93590784	TGAAGGGACCACCCC[A/G]GAGGCCATGGGCTGG	5253
rs2150752	snp	G/T	0.290718	0.246662	intron-variant	PHF2	GRCh38.p7	9:93590837	CTGGTTGTGGTGGTG[G/T]TTTCTGACTCCCCTT	5253
rs2250236	snp	C/T	0.299158	0.245119	intron-variant	PHF2	GRCh38.p7	9:93615515	CCAGTATTTCTGTCA[C/T]TGACCTTCTACTAGA	5253
rs2250344	snp	C/T	0.434398	0.168811	intron-variant	PHF2	GRCh38.p7	9:93614116	ACTTGCCCTCTACCT[C/T]AGACCATGGCCACCT	5253
rs2254389	snp	A/G	0.434543	0.168653	intron-variant	PHF2	GRCh38.p7	9:93604133	TTCTGAGATGGGGAC[A/G]CCCCTCTGAGATGGG	5253
rs2254712	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93601577	TGTGGTTGGCAGGAT[A/G]GTTGGCACCCCCAGG	5253
rs2254715	snp	C/T	0.299664	0.245017	intron-variant	PHF2	GRCh38.p7	9:93601418	TGCTAAGTTTGCAAA[C/T]AGGCTGTGGCAGGTG	5253
rs2265300	snp	A/G	0.470908	0.117046	intron-variant	PHF2	GRCh38.p7	9:93607553	ctctcaaaatgttgg[A/G]attacaggtgtgagc	5253
rs2265573	snp	A/G	0.299158	0.245119	intron-variant	PHF2	GRCh38.p7	9:93607207	TTTACTTCTCCATGT[A/G]AACTTCAGAATCAAT	5253
rs2265574	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93608493	CCCTCTGCTTCTATC[A/G]TCTGAAAGAGACTGT	5253
rs2265575	snp	A/G	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93609482	ATTTTCTGAACTGTT[A/G]TTTGTCTGATAGACT	5253
rs2265576	snp	C/T	0.470908	0.117046	intron-variant	PHF2	GRCh38.p7	9:93609519	ctccttcacttttga[C/T]ggataattttgctgg	5253
rs2274851	snp	C/T	0.291235	0.246576	intron-variant	PHF2	GRCh38.p7	9:93592807	GGGGCCAAGCACCAG[C/T]ACGTGGCCTTGCACC	5253
rs2398845	snp	G/T	0.421842	0.181577	intron-variant	PHF2	GRCh38.p7	9:93603330	CCGACTTAGCTGTGG[G/T]TGTCTACGGCAGGGA	5253
rs2398846	snp	A/T	0.404035	0.196909	intron-variant	PHF2	GRCh38.p7	9:93603461	TAATGCTGGCTCTGG[A/T]CTCCTGTAGGACACA	5253
rs2398847	snp	A/G	0.404209	0.196773	intron-variant	PHF2	GRCh38.p7	9:93603476	ACTCCTGTAGGACAC[A/G]CTGCTGGGGTCACTG	5253
rs2398848	snp	G/T	0.426047	0.177503	intron-variant	PHF2	GRCh38.p7	9:93633903	TTTTCTTTGATCTCC[G/T]CAGCCAGCCCTGAGG	5253
rs2398849	snp	C/G	0.487809	0.0771174	intron-variant	PHF2	GRCh38.p7	9:93636088	CCTTTTCAGGAGGTG[C/G]CTCTCTGGTGGTCTC	5253
rs2398850	snp	C/T	0.0349115	0.127424	intron-variant	PHF2	GRCh38.p7	9:93636172	TCAGGGAATGGAGGA[C/T]ACTGGTGCCATCCAT	5253
rs2398851	snp	A/G	0.495891	0.0451408	intron-variant	PHF2	GRCh38.p7	9:93636226	ACACGAGGTCGAGGT[A/G]GGGGGTTGACTCCTC	5253
rs2398852	snp	A/G	0.0731253	0.176679	intron-variant	PHF2	GRCh38.p7	9:93636374	CCCTGCTGGGGCTGC[A/G]CTGTGTGACCGACCT	5253
rs2398853	snp	C/T	0.490119	0.0695896	intron-variant	PHF2	GRCh38.p7	9:93637160	AGAATCCTAAGTTGG[C/T]GGGTTTTTTTTCTTT	5253
rs2398854	snp	A/C	0.0260105	0.111035	intron-variant	PHF2	GRCh38.p7	9:93645888	GCCCTGGCTGTGTCC[A/C]TGTGTGCCGTGAGCA	5253
rs2398855	snp	A/C	0.498206	0.0298983	intron-variant	PHF2	GRCh38.p7	9:93646898	TTGGGTGTCCATGCA[A/C]AGGGGCTGATTCTGT	5253
rs2398856	snp	C/T	0.421842	0.181577	intron-variant	PHF2	GRCh38.p7	9:93647088	CTGTTTCTGTCTTGC[C/T]GCACAATGCTGGTCA	5253
rs2398861	snp	A/G	0.469049	0.120489	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668465	GCCCCTAAACACCCT[A/G]GGCCCCTCCCGAGGT	5253
rs2398862	snp	A/G	0.0360663	0.129354	intron-variant	PHF2	GRCh38.p7	9:93677416	TTTGCCAGTGATCCC[A/G]GACTCCTGAAGGGTG	5253
rs2895249	snp	A/G	0.349233	0.229462	intron-variant	PHF2	GRCh38.p7	9:93603471	TCTGGACTCCTGTAG[A/G]ACACACTGCTGGGGT	5253
rs2989751	snp	A/G	0.434543	0.168653	intron-variant	PHF2	GRCh38.p7	9:93604365	TTTGAGACGGAGAGC[A/G]AGACTTCTTTATATT	5253
rs2989752	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93605461	caccattgcaatgta[A/G]tacagaagagtttca	5253
rs2989753	snp	A/G	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93613446	CACTTAGGGTTGGCC[A/G]AGGGCCCTAAAACAG	5253
rs2989754	snp	A/G	0.434398	0.168811	intron-variant	PHF2	GRCh38.p7	9:93613875	CACCACACCTGGCCC[A/G]CATTGTCAGACCAGA	5253
rs2989755	snp	A/G	0.470908	0.117046	intron-variant	PHF2	GRCh38.p7	9:93613971	CTGCTGCCTCTACAC[A/G]TCCCTTTCTTGCTGT	5253
rs2989756	snp	C/T	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93616328	CTGGCCTGAAGGGTG[C/T]AAATCTTTTTAAAGC	5253
rs2994365	snp	C/T	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93612092	CTGCAACTTGTGCTC[C/T]TTGCTGAACAATATA	5253
rs2994366	snp	C/G	0.299411	0.245069	intron-variant	PHF2	GRCh38.p7	9:93602180	AAAAGTATGTAAATT[C/G]TTCGTTGAGTATGTA	5253
rs2994367	snp	A/G	0.298905	0.24517	intron-variant	PHF2	GRCh38.p7	9:93613532	AGTAGGTCCCGGTGG[A/G]GATTGGGGTTCTTCT	5253
rs2994368	snp	A/G	0.298905	0.24517	intron-variant	PHF2	GRCh38.p7	9:93614618	CGCAGTCCTGGAGGA[A/G]TGGACATAGCACACT	5253
rs2994369	snp	C/T	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93604231	GCAGGTGCCGGGGAC[C/T]GAGTGAGTGAGTTGG	5253
rs2994370	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93605538	aaacctctgataacc[A/G]ctgatgtttttactg	5253
rs3080731	in-del	-/GGG	0.495963	0.0447464	intron-variant	PHF2	GRCh38.p7	9:93631803	GGTCCTACCTGAGTT[-/GGG]GGGCTTGGGAGGATG	5253
rs3080732	in-del	-/GTCT			intron-variant	PHF2	GRCh38.p7	9:93632941	CTGTGCCCAGAGGCT[-/GTCT]ATGATGCCCCAGTTG	5253
rs3080758	in-del	-/AT	0.418653	0.184544	intron-variant	PHF2	GRCh38.p7	9:93649687	CTCGTGGACACACTC[-/AT]GACACTCACACTGAC	5253
rs3750353	snp	A/G	0.0560246	0.157714	intron-variant	PHF2	GRCh38.p7	9:93653130	CACTGCAGGGGAAAT[A/G]AAAAAGGGAGTCCCA	5253
rs3750354	snp	C/T	0.456707	0.140614	intron-variant	PHF2	GRCh38.p7	9:93653371	CGTGCTCAAGGTGAG[C/T]CACGCCCCTCGGGGC	5253
rs3750355	snp	C/T	0.0410144	0.137204	intron-variant	PHF2	GRCh38.p7	9:93654617	TGTACTAGGGCTTGC[C/T]GGCCCTCATCAAGCT	5253
rs3750356	snp	A/G	0.0689305	0.172377	intron-variant	PHF2	GRCh38.p7	9:93654821	GGCTTGTGTTGTCTC[A/G]TCAGCATGGGCACTC	5253
rs3750357	snp	C/T	0.394171	0.204242	intron-variant	PHF2	GRCh38.p7	9:93659837	ACTGAGAAATGGCAC[C/T]AGCCTCTCTGAAACT	5253
rs3750358	snp	C/T	0.490839	0.0670581	intron-variant	PHF2	GRCh38.p7	9:93662856	GTGGCTCAAGAGAGT[C/T]CCACCAGCCCTCTAT	5253
rs3750359	snp	A/G	0.317933	0.240593	intron-variant	PHF2	GRCh38.p7	9:93663081	GCTTGGTGAGTGTGA[A/G]CAGAGGTGAATCTGT	5253
rs3750360	snp	A/G	0.075454	0.179954	intron-variant	PHF2	GRCh38.p7	9:93663206	TGTGACCACCCATGG[A/G]CTACATCTTCCTCTG	5253
rs3750361	snp	C/T	0.484066	0.0878235	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669538	CACACCTCAATCCTG[C/T]TCAGTCCCTGTGAAA	5253
rs3750362	snp	A/G	0.49998	0.00319482	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669577	GCAACGCAGTCCAGT[A/G]TGTCTCAGACAGGGC	5253
rs3750363	snp	C/T	0.00279162	0.0372561	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669647	TGCCCCGGCACTGGG[C/T]ATCTTCCTGAGTCTG	5253
rs3750364	snp	C/G	0.167809	0.236103	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669851	GAACCAGGACTGGTC[C/G]TGGTGGGGCCACTGC	5253
rs3763605	snp	A/G	0.484672	0.0861922	intron-variant	PHF2	GRCh38.p7	9:93658108	GCACCTGTGGGCAGC[A/G]GGCACCCACCCACCT	5253
rs3813386	snp	C/T	0.0759472	0.179459	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678263	CATTCAGGCTGAACA[C/T]CCACCATCCTGCTGC	5253
rs3829059	snp	C/T	0.0759472	0.179459	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668874	CTCTCCCAAAGTCTC[C/T]CATTTGGAGCGTAGG	5253
rs3829758	snp	A/G	0.390838	0.206555	intron-variant, utr-variant-3-prime	PHF2, LOC107987098	GRCh38.p7	9:93673427	GGCAGTGAGCTGATG[A/G]CTTCTCCCTTGGAAG	5253
rs3922729	snp	C/T	0.462363	0.131916	intron-variant	PHF2	GRCh38.p7	9:93587303	CAACCAGGGCTCCTC[C/T]GTCATCCCTCACCCA	5253
rs3957504	snp	C/T	0.029116	0.117091	intron-variant	PHF2	GRCh38.p7	9:93636061	ACCTGC[C/T]	5253
rs4073155	snp	A/G	0.459118	0.137002	intron-variant	PHF2	GRCh38.p7	9:93592272	AGTTGCCTCTGCAGG[A/G]GCTGCTGGTCCCCAC	5253
rs4146138	snp	C/T	0.290977	0.246619	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593157	ACTGTTCCAGCAGGA[C/T]GGGACATGGCAGCAC	5253
rs4403473	snp	C/G	0.461703	0.132974	intron-variant	PHF2	GRCh38.p7	9:93636892	GCATGCTCCCATGGC[C/G]CAGGCAGGCGTTGTC	5253
rs4568663	snp	A/G	0.404384	0.196635	intron-variant	PHF2	GRCh38.p7	9:93610043	ttgatttttttttgc[A/G]gtttgaatgtgatat	5253
rs4743929	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93606355	aatgaatgagagttc[A/G]tgttgctctacatcc	5253
rs4744255	snp	A/G	0.455502	0.142369	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593656	GAATTCTACACTGTT[A/G]AATGATGAAGTTGGG	5253
rs4744256	snp	C/T	0.142272	0.225598	intron-variant	PHF2	GRCh38.p7	9:93599081	GTCTCAGCGAGCTAG[C/T]CCCGTGTCCATCTCC	5253
rs4744257	snp	A/G	0.434398	0.168811	intron-variant	PHF2	GRCh38.p7	9:93599204	CAGGGTGGGTTCCGA[A/G]GAAGGCCTGCTGGAC	5253
rs4744258	snp	C/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93599287	GCAATGATAGGCAGG[C/G]ATTAGGTGGCACTGG	5253
rs4744259	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93600636	GCCATCTCGCAGGTT[A/G]TGGGATGGTGGCCCT	5253
rs4744261	snp	A/G	0.0221141	0.102801	intron-variant	PHF2	GRCh38.p7	9:93621109	AGGGGTTGGAGCAGC[A/G]ATGCAGATGTAGGGT	5253
rs4744262	snp	A/T	0.00517822	0.0506191	intron-variant	PHF2	GRCh38.p7	9:93628322	gtgttattcttcttt[A/T]aatgtttgatagaat	5253
rs4744263	snp	A/G	0.499965	0.00419314	intron-variant	PHF2	GRCh38.p7	9:93629135	CGAACTCCTGACCTC[A/G]AGTGATCCGCCCACC	5253
rs6479496	snp	G/T	0.469346	0.119947	intron-variant	PHF2	GRCh38.p7	9:93584071	gacctcaggtgatct[G/T]cctgccttggcctcc	5253
rs6479497	snp	A/G			intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593104	AAAAAAAAAAAAAAA[A/G]AAAAAAAGAAAAAAA	5253
rs6479498	snp	A/G	0	0	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593105	AAAAAAAAAAAAAAA[A/G]AAAAAAGAAAAAAAA	5253
rs6479499	snp	A/T	0.496999	0.0386216	intron-variant	PHF2	GRCh38.p7	9:93643582	ATTGCAGCCCTCTAG[A/T]TCCTTGAAGTCTTGT	5253
rs6479500	snp	A/G	0.496034	0.0443518	intron-variant	PHF2	GRCh38.p7	9:93645540	GCCAGACCCAGGCTC[A/G]CCTCTCCAGCACCGA	5253
rs6479501	snp	A/G	0.495963	0.0447464	intron-variant	PHF2	GRCh38.p7	9:93646621	CTCTGTGCACCCTTC[A/G]TGGGGTGTGTGCTGG	5253
rs7018588	snp	A/G	0.264084	0.249603	intron-variant	PHF2	GRCh38.p7	9:93620167	GGAGTGTACAAGGCT[A/G]GGTGGCCAGCGGCCT	5253
rs7018598	snp	C/G	0.499965	0.00419314	intron-variant	PHF2	GRCh38.p7	9:93628965	GCAGTGGTGCAATCT[C/G]GGCTCACTGCAACCT	5253
rs7019081	snp	A/G	0.0209421	0.100162	intron-variant	PHF2	GRCh38.p7	9:93646932	GTTCTTACTGAGGAG[A/G]AGGGCAGGCTGGACA	5253
rs7019745	snp	A/G	0.489837	0.0705577	intron-variant	PHF2	GRCh38.p7	9:93645204	TTCGGTGGCCCTGCC[A/G]TGGGGAGGCACCTAG	5253
rs7022246	snp	A/G	0.104149	0.203046	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593057	AGGTTTCCACATCCT[A/G]ATCTTTGCTTTTCTT	5253
rs7023212	snp	A/C	0.498794	0.0245311	intron-variant	PHF2	GRCh38.p7	9:93580608	TTAAACATCCTTAAC[A/C]TGTAGCTTTCTGGCC	5253
rs7023577	snp	C/T	0.498794	0.0245311	upstream-variant-2KB	PHF2	GRCh38.p7	9:93574711	GCAGCCTCCCCTGCA[C/T]CACAGCAGCCTCTAG	5253
rs7024028	snp	C/T	0.495927	0.0449436	intron-variant	PHF2	GRCh38.p7	9:93632740	TAAATTTTGGTGGGA[C/T]GGATATTCAGTCCAC	5253
rs7025752	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93578024	TGGTCCGGGATTCTC[C/T]TTCCAGAGAGGAGAT	5253
rs7027975	snp	C/T	0.498459	0.0277128	intron-variant	PHF2	GRCh38.p7	9:93590651	CATCTCCACATACCC[C/T]GGCCAGTGTTCCTGA	5253
rs7028306	snp	C/T	0.499598	0.0141716	intron-variant	PHF2	GRCh38.p7	9:93663801	CATCACACACAACCA[C/T]ACACACTGCACATCA	5253
rs7029272	snp	A/G	0.0209421	0.100162	intron-variant	PHF2	GRCh38.p7	9:93644105	GAATTCCAGAGGCTC[A/G]gctgggcgcggtggc	5253
rs7033089	snp	A/G	0.0429648	0.14013	intron-variant	PHF2	GRCh38.p7	9:93583365	gtatatggtgctgct[A/G]taaacatttgtgtat	5253
rs7033146	snp	C/T	0.499137	0.0207489	intron-variant	PHF2	GRCh38.p7	9:93619818	AAAAGGGAAAGGGGC[C/T]GGCCAACTTTGCCTT	5253
rs7033439	snp	C/T	0.385359	0.210185	intron-variant	PHF2	GRCh38.p7	9:93620054	CTGCTCTCCCTCGGA[C/T]TCTGCAGTCCTGGCT	5253
rs7033532	snp	G/T	0.097727	0.198275	intron-variant	PHF2	GRCh38.p7	9:93644962	GATGCTCTTGTCCGG[G/T]TCCTTGGGTTGTCAC	5253
rs7033849	snp	G/T	0.26326	0.249648	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93594664	CTCCCAGTGACAGCA[G/T]GAGTGGGAGAGCACA	5253
rs7036592	snp	C/T	0.440278	0.162155	intron-variant	PHF2	GRCh38.p7	9:93663495	TGTGGGGCTCAGGGA[C/T]GGCCCTGGTCTTGCT	5253
rs7038293	snp	G/T	0.0984431	0.198823	intron-variant	PHF2	GRCh38.p7	9:93646314	GTTAGGTGGGCACTT[G/T]TGGGTAGAGGAAGCA	5253
rs7038310	snp	C/T	0.136934	0.222971	synonymous-codon	PHF2	GRCh38.p7	9:93645638	CTGCAGTGCTGAAGA[C/T]GTGGTGGCCCGTGTG	5253
rs7038444	snp	C/T	0.0486741	0.148216	intron-variant	PHF2	GRCh38.p7	9:93580777	GGCTTGTATTCTGTA[C/T]GGAGTTCAGAGCTGG	5253
rs7038794	snp	C/T	0.0984431	0.198823	intron-variant	PHF2	GRCh38.p7	9:93646675	AAGCCTCTGGGCACA[C/T]AGGGGCACCCACCAG	5253
rs7040175	snp	C/T	0.0460142	0.144533	intron-variant	PHF2	GRCh38.p7	9:93633852	GGGCCCCTGCTGGCT[C/T]CCCTCCGTGGCACCC	5253
rs7040568	snp	A/G	0.293294	0.246223	intron-variant	PHF2	GRCh38.p7	9:93586737	CACGTCCCTCAGTCT[A/G]TCCATCTAGCTGGTG	5253
rs7041943	snp	C/T	0.291493	0.246533	intron-variant	PHF2	GRCh38.p7	9:93587025	GGTGGGAGTTACATT[C/T]TGGCCCCAGTGCAGG	5253
rs7044244	snp	A/G	0.426966	0.176587	intron-variant	PHF2	GRCh38.p7	9:93635407	GGAAGGGCACAATAC[A/G]GGCCCTGCCTGGCTC	5253
rs7044283	snp	G/T	0.290718	0.246662	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93594528	CTTCCTCACCCCAAG[G/T]GTCTACTGCAAGTGG	5253
rs7044896	snp	G/T	0.0166325	0.0896639	intron-variant	PHF2	GRCh38.p7	9:93622712	ctgacctccagCCTG[G/T]AGAGTGAATCCTTCA	5253
rs7044920	snp	A/G	0.0111196	0.0737302	intron-variant, downstream-variant-500B	PHF2, MIR548AU	GRCh38.p7	9:93595013	TGCCAATCACCAGCA[A/G]GTACTCAGGTACTTA	5253
rs7045506	snp	C/T	0.111224	0.207945	intron-variant	PHF2	GRCh38.p7	9:93652584	ATGTGAGCCACCATG[C/T]CCAGCCTAGTTTGAC	5253
rs7849020	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93583821	tgtatcctttttttt[C/T]ttttctttttttttt	5253
rs7849752	snp	G/T	0.499992	0.00199679	intron-variant	PHF2	GRCh38.p7	9:93629708	CAGGCTTGGTAGATG[G/T]CCTATTCATTGGGTC	5253
rs7850596	snp	G/T	0.0596104	0.162024	intron-variant	PHF2	GRCh38.p7	9:93630355	GAGTTAGGGGGACAC[G/T]GACTTGGGGACCTGG	5253
rs7851178	snp	A/T	0.426966	0.176587	intron-variant	PHF2	GRCh38.p7	9:93651423	TAGGGGGTTGTTTGC[A/T]ACTTTTGTTGGGCAC	5253
rs7851271	snp	A/G	0.421842	0.181577	intron-variant	PHF2	GRCh38.p7	9:93645566	ACCGAGGCCCTGTCC[A/G]CACCTGTCCCGGTGC	5253
rs7854758	snp	C/T	0.0970103	0.197722	intron-variant	PHF2	GRCh38.p7	9:93610895	GCCAGGCAGTGATTG[C/T]TGAAGGATTGAAAGT	5253
rs7856259	snp	A/G	0.097727	0.198275	intron-variant	PHF2	GRCh38.p7	9:93619344	TGATCCTCACTGGCC[A/G]AGGAGGACTTGCTCA	5253
rs7857165	snp	A/T	0.291235	0.246576	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593698	AATGACAGTGTCCTC[A/T]TGTAAATCGGAAATT	5253
rs7857266	snp	C/T	0.422944	0.180528	intron-variant	PHF2	GRCh38.p7	9:93619483	AGGCCAAGAAGGCGA[C/T]TCGTGGGGTGGTGGA	5253
rs7864091	snp	A/G	0.284209	0.247648	intron-variant	PHF2	GRCh38.p7	9:93583906	tgatctcagctcacc[A/G]caacctctgcctccc	5253
rs7864397	snp	A/G	0.426966	0.176587	intron-variant	PHF2	GRCh38.p7	9:93651399	CCACTGGCCCAGTCC[A/G]TGGATCATTAGGGGG	5253
rs7865712	snp	A/G	0.447162	0.153712	intron-variant	PHF2	GRCh38.p7	9:93629737	TCCTCATGGTGGGGC[A/G]TATCCAGACGCTGTA	5253
rs7868191	snp	A/T	0.435263	0.167862	intron-variant	PHF2	GRCh38.p7	9:93642461	tatgaaaatacatac[A/T]gtcttgtctgacaat	5253
rs7869286	snp	C/T	0.299158	0.245119	intron-variant	PHF2	GRCh38.p7	9:93602452	GAGATGGGGTTTTAC[C/T]GTGTTGCCCAGGCTG	5253
rs7869847	snp	A/C	0.233527	0.249457	intron-variant	PHF2	GRCh38.p7	9:93630746	TGGTTGCAGAGGGGG[A/C]GCTGTGTGGTGGTCT	5253
rs7872863	snp	C/T	0.309894	0.242719	intron-variant	PHF2	GRCh38.p7	9:93630533	CATGCCACCCACCTC[C/T]TCCTCTGCAGAGAAT	5253
rs7873003	snp	C/T	0.495891	0.0451408	intron-variant	PHF2	GRCh38.p7	9:93630663	GGGATACAGGCTTGG[C/T]TCACCCTGTGCAGGT	5253
rs9299409	snp	A/G	0.299158	0.245119	intron-variant	PHF2	GRCh38.p7	9:93607798	AAGTGTTCATTTCTG[A/G]TAAATAAGAAAGCAA	5253
rs9409477	snp	C/T	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93606481	tgtggaacatctttt[C/T]atgtacttatttgct	5253
rs9409478	snp	A/G	0.141596	0.225274	intron-variant	PHF2	GRCh38.p7	9:93617223	CACTCAAGTCCTCAT[A/G]GGAGGCTGCACCCTG	5253
rs9644969	snp	C/T	0.499087	0.0213463	intron-variant	PHF2	GRCh38.p7	9:93586641	TCCTGAGTCTCAAAA[C/T]GGCCCAGGAATCCAG	5253
rs9644970	snp	C/G	0.0737376	0.17729	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93667460	TTCTTTTAATTTTTC[C/G]GGTAAATTCAGAACC	5253
rs9695734	snp	C/T	0.228596	0.249082	synonymous-codon	PHF2	GRCh38.p7	9:93645701	GGAGCACGGCTTCAC[C/T]GAGCCCATCCTCGTC	5253
rs10114002	snp	C/T	0.480618	0.0965156	intron-variant	PHF2	GRCh38.p7	9:93595748	GCGTAACCAGAGATG[C/T]CTTCCTCTTGATGGA	5253
rs10114689	snp	C/G	0.292008	0.246445	intron-variant	PHF2	GRCh38.p7	9:93589589	CACTTGGAAATTAAA[C/G]TCAGTGACCCACCTG	5253
rs10115715	snp	A/T	0.189261	0.242509	intron-variant	PHF2	GRCh38.p7	9:93639523	catttgcaaattgag[A/T]tagtatgacttattc	5253
rs10116422	snp	A/C	0.480775	0.0961398	intron-variant	PHF2	GRCh38.p7	9:93595457	GACGGTAAGGAATTT[A/C]TGAAAATATAATGTA	5253
rs10116955	snp	A/T	0.282895	0.247826	intron-variant, downstream-variant-500B	PHF2, MIR548AU	GRCh38.p7	9:93595110	TTTGGGTGCTTATCT[A/T]TAAAGGGGTACTTAC	5253
rs10116959	snp	A/G	0.0966517	0.197444	intron-variant	PHF2	GRCh38.p7	9:93601249	TTTGGCTGTCTGCAC[A/G]TATACAGCCAGGGAC	5253
rs10117225	snp	C/T	0.404559	0.196498	intron-variant	PHF2	GRCh38.p7	9:93605063	ACAGAGTGAAAAGAT[C/T]GAGAGTTCCCACATA	5253
rs10117691	snp	C/T	0.480618	0.0965156	intron-variant	PHF2	GRCh38.p7	9:93595643	ACACAGACCGAGATT[C/T]GCATCTTCTGTGAAC	5253
rs10118129	snp	C/T	1.67075e-05	0.00289023	intron-variant	PHF2	GRCh38.p7	9:93656618	TCACTCCGGGGTGGG[C/T]GTCCAAGCCTGGGGC	5253
rs10118281	snp	A/G	0.0391387	0.134304	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93594163	GATATCTGCCCTTCC[A/G]GCACACCCCCTCTTC	5253
rs10119832	snp	A/G	0.26326	0.249648	intron-variant	PHF2	GRCh38.p7	9:93595644	CACAGACCGAGATTT[A/G]CATCTTCTGTGAACA	5253
rs10121780	snp	C/T	0.233527	0.249457	intron-variant	PHF2	GRCh38.p7	9:93631145	TCCAGCACCCCTGTT[C/T]TGTGAGCTGAGGCTG	5253
rs10122014	snp	C/T	0.290977	0.246619	intron-variant	PHF2	GRCh38.p7	9:93591203	TTGTCTGGCCCTGAC[C/T]GTGTCTGTCATAACC	5253
rs10122030	snp	C/T	0.290201	0.246747	intron-variant	PHF2	GRCh38.p7	9:93591220	TGTCTGTCATAACCA[C/T]TTATGGCCACAGATG	5253
rs10122092	snp	C/T	0.498459	0.0277128	intron-variant	PHF2	GRCh38.p7	9:93591465	ACCATGTGAGTAGGA[C/T]GTGTGGACTGGGGGC	5253
rs10122270	snp	A/G	0.447421	0.153379	intron-variant	PHF2	GRCh38.p7	9:93627849	AGAGATGGGAACATA[A/G]GAATGAGGCAGAGGG	5253
rs10123378	snp	C/T	0.418169	0.184985	intron-variant	PHF2	GRCh38.p7	9:93612935	GGGACTTCTCTCTAA[C/T]TGCACCCTTCACGTG	5253
rs10123412	snp	A/C/G	0.104149	0.203046	intron-variant	PHF2	GRCh38.p7	9:93589198	AGGAACCAAGTGCTC[A/C/G]CTGAAAGTTTGGAGC	5253
rs10124411	snp	A/G	0.426966	0.176587	intron-variant	PHF2	GRCh38.p7	9:93614874	GGTGATGATGGTGAC[A/G]GTGATGGTGATGGTG	5253
rs10156602	snp	A/G	0.422944	0.180528	intron-variant	PHF2	GRCh38.p7	9:93583046	TAAACCCGGTATCCA[A/G]TAAGTAGTCACTGCC	5253
rs10739951	snp	C/T	0.421526	0.181876	intron-variant	PHF2	GRCh38.p7	9:93599303	ATTAGGTGGCACTGG[C/T]GTGGCTGGAGAGTGG	5253
rs10739952	snp	G/T	0.299158	0.245119	intron-variant	PHF2	GRCh38.p7	9:93599931	TTTATCAGTGAAGAC[G/T]TTGAGGCCAAGAAAG	5253
rs10761237	snp	C/T	0.499961	0.0043928	intron-variant	PHF2	GRCh38.p7	9:93578535	CGAGCGCAGTCACTC[C/T]GCTACAGAACCTTCT	5253
rs10761238	snp	C/T	0.345925	0.230864	intron-variant	PHF2	GRCh38.p7	9:93588935	TATGAAGTCTCTGTT[C/T]GTGGCCCTGAAGGCA	5253
rs10761239	snp	C/T	0.421684	0.181726	intron-variant	PHF2	GRCh38.p7	9:93597602	CTATGGCTTGGCTGC[C/T]CGGCTTGAGTTTCAG	5253
rs10761240	snp	A/G	0.404559	0.196498	intron-variant	PHF2	GRCh38.p7	9:93599640	TCAGCCGAGATATTC[A/G]GTGGTTACCTGTGAG	5253
rs10761241	snp	C/T	0.350327	0.228986	intron-variant	PHF2	GRCh38.p7	9:93606254	GGATTACAGGCTGGG[C/T]GCCACCATGCCCAGC	5253
rs10761242	snp	C/T	0.404384	0.196635	intron-variant	PHF2	GRCh38.p7	9:93606374	TGCTCTACATCCTTG[C/T]CAGCATTTGGTGTTG	5253
rs10761243	snp	G/T	0.421842	0.181577	intron-variant	PHF2	GRCh38.p7	9:93606976	TCTCCGTTGTATTGC[G/T]TTTGTTCCTTTTTCT	5253
rs10761244	snp	C/T	0.471004	0.116864	intron-variant	PHF2	GRCh38.p7	9:93625310	AGGATGTATCAGGAC[C/T]TCATTCCTTTTTAAG	5253
rs10761245	snp	C/T	0.471004	0.116864	intron-variant	PHF2	GRCh38.p7	9:93625393	CTGTCAGTGGACATT[C/T]GGGCAATTTCCACTT	5253
rs10761246	snp	C/T	0.470908	0.117046	intron-variant	PHF2	GRCh38.p7	9:93625513	GACAGAGTCTTGCTT[C/T]ATTGGCCAGGCTTGA	5253
rs10761247	snp	A/G	0.499673	0.0127754	intron-variant	PHF2	GRCh38.p7	9:93641085	CAGGATTAAATCTCA[A/G]TTTTGTAGAGTCTCT	5253
rs10761248	snp	A/C	0.498253	0.0295011	intron-variant	PHF2	GRCh38.p7	9:93645235	CCGAGAAGGGGTACA[A/C]GGGAGGTGCAGTGGA	5253
rs10761249	snp	A/T	0.426966	0.176587	intron-variant	PHF2	GRCh38.p7	9:93650910	GGGAGAAACAAAAGA[A/T]TTATCTAAAACCAAG	5253
rs10761250	snp	A/C	0.383632	0.211288	intron-variant	PHF2	GRCh38.p7	9:93657494	GCACCTGGGAAGCCA[A/C]CCCACAGGGCCAGCC	5253
rs10761251	snp	A/T	0.499539	0.0151687	intron-variant	PHF2	GRCh38.p7	9:93659264	GAAGGGATGGGACCC[A/T]TGTCCATTCCATAGC	5253
rs10761252	snp	A/G	0.499598	0.0141716	intron-variant	PHF2	GRCh38.p7	9:93662019	AATGGATGGATGGGT[A/G]GATGATGAATGAATC	5253
rs10761253	snp	A/G	0.0539704	0.155153	intron-variant	PHF2	GRCh38.p7	9:93664013	ACATGCCTGGGTGGG[A/G]CTGGGCTGGAAGATA	5253
rs10761254	snp	C/T	0.499598	0.0141716	intron-variant	PHF2	GRCh38.p7	9:93664062	GGATGGCCCCCCAGG[C/T]AGGGAGGGAGGCCGT	5253
rs10761255	snp	A/G	0.499977	0.00339449	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93670902	GGGCAGCGGGGGTGC[A/G]GACAGGGCAAAGAGA	5253
rs10821161	snp	C/T	0.0777841	0.181223	upstream-variant-2KB	PHF2	GRCh38.p7	9:93576100	ATCTTATCCTCGGGG[C/T]CCCGCCCACCTTCTC	5253
rs10821162	snp	G/T	0.498794	0.0245311	intron-variant	PHF2	GRCh38.p7	9:93579042	TGCCTGCTCCCCAAT[G/T]GTTCTGGGCAGGTGT	5253
rs10821163	snp	C/G	0.349671	0.229272	intron-variant	PHF2	GRCh38.p7	9:93580778	GCTTGTATTCTGTAC[C/G]GAGTTCAGAGCTGGC	5253
rs10821164	snp	C/T	0.403158	0.197592	intron-variant	PHF2	GRCh38.p7	9:93584947	TTACAAGTCTTTCAC[C/T]GACTCAGTTACATTT	5253
rs10821165	snp	C/T	0.411578	0.190768	intron-variant	PHF2	GRCh38.p7	9:93589352	CCTCTGCACGGCTGA[C/T]GTCTGGGCTGGAGAA	5253
rs10821166	snp	A/G	0.411578	0.190768	intron-variant	PHF2	GRCh38.p7	9:93589641	TTTGATAAGGCATCA[A/G]CTACATTTATTCATT	5253
rs10821167	snp	A/G	0.412249	0.190198	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593722	GGAAATTATGCAGTC[A/G]TCAGCAGTGATGTTT	5253
rs10821168	snp	C/T	0.370772	0.218893	intron-variant	PHF2	GRCh38.p7	9:93596019	TTGCTGGCTTACCCA[C/T]GGTCTGTCCTCATGG	5253
rs10821169	snp	C/T	0.424968	0.178567	intron-variant	PHF2	GRCh38.p7	9:93598837	ATACAGGAATGCATT[C/T]CCCTAAGAAGCCCAT	5253
rs10821170	snp	C/T	0.472335	0.114312	intron-variant	PHF2	GRCh38.p7	9:93599766	GGGGGATTCGGAGCA[C/T]GAAAGGGATTTAGAG	5253
rs10821171	snp	C/T	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93599953	CCAAGAAAGATAGGA[C/T]GTCCACGGCCCTCAT	5253
rs10821172	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93599969	GTCCACGGCCCTCAT[A/G]CTGCCCAGGAACAGC	5253
rs10821173	snp	C/G	0.421684	0.181726	intron-variant	PHF2	GRCh38.p7	9:93600173	TGTGCAGTTTGTGTG[C/G]TGTGTGTCTGTAGCA	5253
rs10821174	snp	A/G	0.421526	0.181876	intron-variant	PHF2	GRCh38.p7	9:93600347	GAGGCAGCTCCTGGA[A/G]GGCAGGGCACTCAGT	5253
rs10821175	snp	C/T	0.349671	0.229272	intron-variant	PHF2	GRCh38.p7	9:93601365	TAGTTAAGGTTGGTT[C/T]GGGCTTGAGAGGGAA	5253
rs10821176	snp	C/T	0.421684	0.181726	intron-variant	PHF2	GRCh38.p7	9:93602174	TCGAACAAAAGTATG[C/T]AAATTCTTCGTTGAG	5253
rs10821177	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93605304	CTCACTGTAACCTCT[A/G]AAGGCTGGACTCAAG	5253
rs10821179	snp	A/C	0.349233	0.229462	intron-variant	PHF2	GRCh38.p7	9:93607214	CTCCATGTAAACTTC[A/C]GAATCAATTTGTCAA	5253
rs10821180	snp	C/T	0.349233	0.229462	intron-variant	PHF2	GRCh38.p7	9:93607487	AGGGTTTCACCATGT[C/T]GCCCAGGCTGGTCTC	5253
rs10821181	snp	C/T	0.349233	0.229462	intron-variant	PHF2	GRCh38.p7	9:93617201	CCCCTGAAGGCAACC[C/T]CTAGCCCACTCAAGT	5253
rs10821182	snp	C/T	0.25214	0.249991	intron-variant	PHF2	GRCh38.p7	9:93621093	TGGTGGCACAGGCAG[C/T]AGGGGTTGGAGCAGC	5253
rs10821183	snp	A/G	0.198944	0.244731	intron-variant	PHF2	GRCh38.p7	9:93621323	GAGCTTCTTTTGGGC[A/G]GCAGAAGGACCCTTC	5253
rs10821184	snp	A/G	0.471004	0.116864	intron-variant	PHF2	GRCh38.p7	9:93625623	GCTAGGGCCACAGGT[A/G]TGTGTCACCATGCCC	5253
rs10821185	snp	C/T	0.388964	0.20782	intron-variant	PHF2	GRCh38.p7	9:93636717	TGCAAATGGGCCAAC[C/T]TCTCCTTCCCTTGGT	5253
rs10821186	snp	A/G	0.405429	0.195811	intron-variant	PHF2	GRCh38.p7	9:93638763	TCACTCTGTCACCCA[A/G]GCTGGAGTACAGTAG	5253
rs10821187	snp	A/G	0.421842	0.181577	intron-variant	PHF2	GRCh38.p7	9:93644576	TCGGCCCTGTCTTGC[A/G]GGGTGCTCTTTCCCC	5253
rs10821188	snp	A/G	0.421842	0.181577	intron-variant	PHF2	GRCh38.p7	9:93644891	CTGTGGGCCCCTCTC[A/G]TCTGCCTCTGGCCCT	5253
rs10821189	snp	A/G	0.422158	0.181278	intron-variant	PHF2	GRCh38.p7	9:93645232	TAGCCGAGAAGGGGT[A/G]CAAGGGAGGTGCAGT	5253
rs10821190	snp	A/G	0.426966	0.176587	intron-variant	PHF2	GRCh38.p7	9:93652372	TGATTTTGGCTCACT[A/G]TAACCTCTGCCTCCT	5253
rs10821191	snp	C/T	0.426966	0.176587	intron-variant	PHF2	GRCh38.p7	9:93652653	GACATGTCATTGAAT[C/T]GAAGGCTGCCTCTGC	5253
rs10821192	snp	C/T	0.317692	0.240661	intron-variant	PHF2	GRCh38.p7	9:93655148	TTTCTGAAGGGCTTC[C/T]TTTCCTTCTAAGTAA	5253
rs10821193	snp	A/G	0.383824	0.211166	intron-variant	PHF2	GRCh38.p7	9:93658939	CTCGAGCACCCTCTG[A/G]GACAGTGTTTCCTAC	5253
rs10821194	snp	C/T	0.384017	0.211044	intron-variant	PHF2	GRCh38.p7	9:93658987	GGTACTATGCCCACT[C/T]TTGAGGGAGGAGGAC	5253
rs10821195	snp	C/G	0.384593	0.210677	intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93671067	GGTGTAGATGCAGGT[C/G]GGGGTGCAGGGTGGG	5253
rs10821196	snp	A/G	0.490398	0.0686206	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671114	GACGCAGGTGGGGGT[A/G]CATGTGTGGGGGTAG	5253
rs10821197	snp	A/T			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671402	CAGGTGTAGATGCAG[A/T]TGTGGGTGTGGATGT	5253
rs10821199	snp	A/G/T			synonymous-codon	PHF2	GRCh38.p7	9:93676707	ctccacctccaccac[A/G/T]ccagcctctaccacc	5253
rs10821200	snp	A/G			synonymous-codon	PHF2	GRCh38.p7	9:93676710	cacctccaccacgcc[A/G]gcctctaccaccccg	5253
rs10821201	snp	C/T	0.5	0	synonymous-codon	PHF2	GRCh38.p7	9:93676716	CACCACGCCAGCCTC[C/T]ACCACCCCGGCCTCC	5253
rs10992789	snp	C/T	0.498774	0.02473	intron-variant	PHF2	GRCh38.p7	9:93578914	CCTATTTGGGGTGGC[C/T]GTGGGGTCTGAAAGA	5253
rs10992790	snp	C/T	0.332337	0.236052	intron-variant	PHF2	GRCh38.p7	9:93579075	GATGGGGAGGACAGC[C/T]GTCAGGGGTTGGTGG	5253
rs10992791	snp	A/G	0.459118	0.137002	intron-variant	PHF2	GRCh38.p7	9:93587851	TCCCTGGAGCTGCCC[A/G]TTGGCCTCACTGACC	5253
rs10992792	snp	A/T	0.303438	0.244222	intron-variant	PHF2	GRCh38.p7	9:93589961	ACTTCCTGCTTCCCC[A/T]GGTTGGCATGTAGCT	5253
rs10992793	snp	A/G	0	0	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93594776	TGGACACCAGCCTTA[A/G]TCCACACCGGCTGAG	5253
rs10992794	snp	A/C	0.453697	0.14494	intron-variant	PHF2	GRCh38.p7	9:93596822	GGAGTGCAATGGTGC[A/C]ATCTTGGCTTACTGC	5253
rs10992795	snp	A/G	0.464841	0.127841	intron-variant	PHF2	GRCh38.p7	9:93597226	GAGCCATCGCGCCTG[A/G]CCTCTGCCAAGTTTT	5253
rs10992796	snp	C/G	0.467744	0.122832	intron-variant	PHF2	GRCh38.p7	9:93598623	CCTAAGAGGTTGTTC[C/G]TGAGTATCAGGGCGG	5253
rs10992797	snp	A/G	0.404384	0.196635	intron-variant	PHF2	GRCh38.p7	9:93599833	CACGCTCCCAGTTCC[A/G]TTGATCTGAAACTCG	5253
rs10992798	snp	A/G	0.421526	0.181876	intron-variant	PHF2	GRCh38.p7	9:93599923	CCTTTGTCTTTATCA[A/G]TGAAGACTTTGAGGC	5253
rs10992799	snp	C/T	0.421526	0.181876	intron-variant	PHF2	GRCh38.p7	9:93601636	TGGTCCCAGGGAAGA[C/T]CAGGGGATGGCTCAG	5253
rs10992800	snp	A/G	0.31721	0.240796	intron-variant	PHF2	GRCh38.p7	9:93611536	TATTTTTTAATACAG[A/G]GTCTTGCTCTGTCAC	5253
rs10992801	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93615187	atagtaatggtgatg[A/G]cgatggtgatgatga	5253
rs10992802	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93615210	gatgatgatggtgat[A/G]gtgatggtgatagta	5253
rs10992803	snp	A/T	0.422787	0.180679	intron-variant	PHF2	GRCh38.p7	9:93615244	gtgatggtgatggtg[A/T]tgatggtgatggtga	5253
rs10992804	snp	G/T	0.419135	0.184101	intron-variant	PHF2	GRCh38.p7	9:93618070	CCCACTCACCTCTGT[G/T]TTTGAAATTTCTATT	5253
rs10992805	snp	G/T	0.328382	0.237395	intron-variant	PHF2	GRCh38.p7	9:93619634	ATGCCTGCTGGTGGC[G/T]TCCGGTAGCCCGTGC	5253
rs10992806	snp	C/G	0.484209	0.0874434	intron-variant	PHF2	GRCh38.p7	9:93621190	TCAGCCTTGGAGGGG[C/G]AGGAGGGGCAGCCCA	5253
rs10992807	snp	C/G	0.458775	0.137524	intron-variant	PHF2	GRCh38.p7	9:93626865	GCATGGTCTAGGAAC[C/G]CTTGTCAAAAATCAG	5253
rs10992808	snp	C/T	0.0678174	0.1712	intron-variant	PHF2	GRCh38.p7	9:93628937	AGTCTCATTCTGTTG[C/T]CCAGGCTGGAGTGCA	5253
rs10992809	snp	C/T	0.0678174	0.1712	intron-variant	PHF2	GRCh38.p7	9:93629058	TGTGCCACTGTGCTC[C/T]GGCTAATTTTTTTTG	5253
rs10992810	snp	C/T	0.00279162	0.0372561	intron-variant	PHF2	GRCh38.p7	9:93629746	TGGGGCATATCCAGA[C/T]GCTGTATCTAGGTCC	5253
rs10992811	snp	G/T	0.0829062	0.185956	intron-variant	PHF2	GRCh38.p7	9:93629747	GGGGCATATCCAGAC[G/T]CTGTATCTAGGTCCA	5253
rs10992812	snp	A/G	0.375	0.216506	intron-variant	PHF2	GRCh38.p7	9:93629900	GGGATTCTCCCTAGA[A/G]CTTCGCAGATGGAAA	5253
rs10992813	snp	A/G	0.420878	0.182485	intron-variant	PHF2	GRCh38.p7	9:93630089	GCGGCCATCTCTTGC[A/G]GAAGAGAGCAGCATC	5253
rs10992814	snp	A/G	0.0670745	0.170406	intron-variant	PHF2	GRCh38.p7	9:93633327	GATTTGGTACAGGGT[A/G]TCCCAAGGTACCTGG	5253
rs10992815	snp	A/G	0.318174	0.240525	intron-variant	PHF2	GRCh38.p7	9:93635127	GGCCTTGACTCTGTC[A/G]GATTTTGCCAAGTTT	5253
rs10992816	snp	G/T	0.0655868	0.168795	intron-variant	PHF2	GRCh38.p7	9:93635177	TGTGGGCAGGGAGAT[G/T]GAACACAATGCGAAG	5253
rs10992817	snp	G/T	0.189261	0.242509	intron-variant	PHF2	GRCh38.p7	9:93636081	CTGAGGACCTTTTCA[G/T]GAGGTGGCTCTCTGG	5253
rs10992818	snp	C/G	0.271582	0.249067	intron-variant	PHF2	GRCh38.p7	9:93636549	GCCTTCCTGTATGCT[C/G]CACCACCTGCAGCCA	5253
rs10992819	snp	A/G	0.405776	0.195535	intron-variant	PHF2	GRCh38.p7	9:93636902	ATGGCCCAGGCAGGC[A/G]TTGTCCTCATGTCTC	5253
rs10992820	snp	G/T	0.255224	0.249945	intron-variant	PHF2	GRCh38.p7	9:93640579	CTTAATTTCCATTTC[G/T]CTGTTTACATTACCC	5253
rs10992821	snp	G/T	0.0655868	0.168795	intron-variant	PHF2	GRCh38.p7	9:93641828	TTATTGCTTGTGCTT[G/T]TGGTATCACTGCTGA	5253
rs10992822	snp	A/C	0.0588605	0.161139	intron-variant	PHF2	GRCh38.p7	9:93646546	AGGCAGGCACACTGG[A/C]CTCTCAGTGCTGGGG	5253
rs10992823	snp	C/T	0.0588605	0.161139	intron-variant	PHF2	GRCh38.p7	9:93646596	CACCACTCTGAGGCT[C/T]ACTCTCTTCCTCTGT	5253
rs10992824	snp	C/T	0.0659589	0.169201	intron-variant	PHF2	GRCh38.p7	9:93647950	TCTAGTACATAGCTC[C/T]AGCAGACAATTTAAA	5253
rs10992825	snp	A/G	0	0	intron-variant	PHF2	GRCh38.p7	9:93649531	CCATCCCACTCCTCA[A/G]AGAGAACCATTGGTA	5253
rs10992826	snp	C/T	0.0744748	0.178019	intron-variant	PHF2	GRCh38.p7	9:93651323	GGAGCTAGGGAGAGA[C/T]GGTACTTTGGCCTGT	5253
rs10992827	snp	C/T	0.093777	0.195178	intron-variant	PHF2	GRCh38.p7	9:93652805	AGGTGCCGGGCTGAG[C/T]GTGAGAAATGATATC	5253
rs10992828	snp	A/G	0.244205	0.249933	intron-variant	PHF2	GRCh38.p7	9:93653086	AGGTGGTGAGAGAGC[A/G]TGGGACATGCCTCAC	5253
rs10992829	snp	C/T	0.384209	0.210922	intron-variant	PHF2	GRCh38.p7	9:93653701	CCATAGCCAGGGCCC[C/T]GCACAGGAGCCAGGG	5253
rs10992830	snp	A/C	0.0689305	0.172377	intron-variant	PHF2	GRCh38.p7	9:93656255	GGATGGTTGTAGTTG[A/C]CCTTGGTGGGGTTGG	5253
rs10992831	snp	A/G	0.393987	0.204372	intron-variant	PHF2	GRCh38.p7	9:93656803	CTCTCCTTCCGATTG[A/G]ACTGTCCCTTGTTTT	5253
rs10992832	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93658054	TCTGGAAGGCTGGAC[C/T]TGGCATCCCCCGGTC	5253
rs10992833	snp	C/G	0.0659589	0.169201	intron-variant	PHF2	GRCh38.p7	9:93658940	TCGAGCACCCTCTGG[C/G]ACAGTGTTTCCTACT	5253
rs10992834	snp	C/T	0.0689305	0.172377	intron-variant	PHF2	GRCh38.p7	9:93659243	GGAGTGGCCTCTGAC[C/T]AGGAAGAAGGGATGG	5253
rs10992835	snp	A/G	0.0115144	0.0749975	intron-variant	PHF2	GRCh38.p7	9:93659746	TCCTTGCACTTTCCT[A/G]GGCAAGCTTGCCTTT	5253
rs10992836	snp	C/T	0.499598	0.0141716	intron-variant	PHF2	GRCh38.p7	9:93660138	GGTGTGTGGACCGTC[C/T]TGGGCCACAGTTTGG	5253
rs10992837	snp	A/C/G	0.0132746	0.080381	missense	PHF2	GRCh38.p7	9:93660207	AATGCCTCCAAAGCC[A/C/G]TCCGACCGGAAGTGA	5253
rs10992838	snp	A/G	0.0737376	0.17729	intron-variant	PHF2	GRCh38.p7	9:93665058	GGGAAGGCAAAGGCT[A/G]GAGCTGCTTGCAGGC	5253
rs10992839	snp	C/T	0.381891	0.212379	intron-variant	PHF2	GRCh38.p7	9:93665223	AACTTGGGTCCTTTT[C/T]CGGTTAAAGACCAAT	5253
rs10992840	snp	A/G	0.392881	0.205147	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666175	TCTGCATGAGATGGC[A/G]AAGGGGCCCCTTACC	5253
rs10992841	snp	C/T	0.499137	0.0207489	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93667833	CTGGGCAGTGATATC[C/T]GGGTGTTTGCGGCTG	5253
rs10992842	snp	G/T	0.39121	0.2063	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93667840	GTGATATCCGGGTGT[G/T]TGCGGCTGGTCCCTT	5253
rs10992843	snp	A/G	0.167158	0.235875	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669392	ACTGCGCTCACTTAG[A/G]CAGGCCTTCAGTGCT	5253
rs10992845	snp	A/G	0.227959	0.249026	intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93671148	TAGGTGCAGATGCAG[A/G]TGTGGATGTAGGTGT	5253
rs10992847	snp	A/T			intron-variant	PHF2, LOC107987098	GRCh38.p7	9:93671485	AGATGTGGGTGTGGG[A/T]GTAGGTACAGGTGTA	5253
rs10992848	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671544	CAGGTGTAGATGCAG[A/G]TGTGGGTGTGGGAGT	5253
rs10992849	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671556	CAGATGTGGGTGTGG[A/G]AGTAGGGTCAGGTGT	5253
rs10992850	snp	A/T			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93671557	AGATGTGGGTGTGGG[A/T]GTAGGGTCAGGTGTA	5253
rs10992851	snp	G/T			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93671563	GGGTGTGGGAGTAGG[G/T]TCAGGTGTAGATGCA	5253
rs10992852	snp	A/T			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671564	GGTGTGGGAGTAGGG[A/T]CAGGTGTAGATGCAG	5253
rs10992853	snp	G/T	0.393065	0.205018	intron-variant	PHF2	GRCh38.p7	9:93674643	GGGGCTTGCAGGCAC[G/T]GGGGCTAGGCTGCAC	5253
rs10992854	snp	C/T	0.498908	0.0233371	intron-variant	PHF2	GRCh38.p7	9:93675283	CCTCACTCCTCTGGC[C/T]GGCTCCTCTCTGGTT	5253
rs10992855	snp	A/G/T	0.00744415	0.0605654	synonymous-codon	PHF2	GRCh38.p7	9:93676725	AGCCTCTACCACCCC[A/G/T]GCCTCCACCACCCCG	5253
rs10992856	snp	A/C	0.00188608	0.030651	synonymous-codon	PHF2	GRCh38.p7	9:93676737	CCCGGCCTCCACCAC[A/C]CCGGCCTCCACCAGC	5253
rs10992857	snp	C/G	0.000493218	0.015696	missense	PHF2	GRCh38.p7	9:93676751	ccccggcctccacca[C/G]cacggccagcaGCCA	5253
rs10992858	snp	A/C	0.000393546	0.0140221	missense	PHF2	GRCh38.p7	9:93676753	ccggcctccaccagc[A/C]cggccagcaGCCAGG	5253
rs10992859	snp	A/G	0.040671	0.13668	intron-variant	PHF2	GRCh38.p7	9:93677054	TCGGCCCATGGTAGA[A/G]GGCAGCACATTGGGA	5253
rs11534279	snp	A/G	0.472052	0.11486	intron-variant	PHF2	GRCh38.p7	9:93639182	ATTTCCATCTTAACA[A/G]TGTTAAAACCTCTAA	5253
rs11791195	snp	C/G	0.00199481	0.0315187	intron-variant	PHF2	GRCh38.p7	9:93613045	TTCCTGGTCACAGAG[C/G]TTTAGCTGTCTGGGG	5253
rs11791934	snp	A/G	0.404907	0.196224	intron-variant	PHF2	GRCh38.p7	9:93602473	GCCCAGGCTGGTCTC[A/G]AACTCCTGAGCTCCG	5253
rs11793637	snp	A/G	0.488302	0.0755777	intron-variant	PHF2	GRCh38.p7	9:93653617	TAACAATTGGGTGAG[A/G]CCACCAGGTGACCAT	5253
rs11795351	snp	C/G			intron-variant	PHF2	GRCh38.p7	9:93629178	agtgctgggattaca[C/G]acatgagccaccgtg	5253
rs12002044	snp	C/G	0.471388	0.116136	intron-variant	PHF2	GRCh38.p7	9:93627579	TAGGCATCCTATTTT[C/G]CTCCTCATCTTATGG	5253
rs12002634	snp	A/C	0	0	intron-variant	PHF2	GRCh38.p7	9:93659085	AATACCATGTGTAGC[A/C]TGCCTTTCTCATGGG	5253
rs12235863	snp	C/T	0.0659589	0.169201	intron-variant	PHF2	GRCh38.p7	9:93649674	CTCATGACACCCACT[C/T]GTGGACACACTCATG	5253
rs12237139	snp	C/T	0.0696718	0.173152	intron-variant	PHF2	GRCh38.p7	9:93649810	GTCACACACCTGCAG[C/T]CATGACACACTCATA	5253
rs12238449	snp	C/T	0.00159617	0.0282053	intron-variant	PHF2	GRCh38.p7	9:93654803	CAGAGGGGCCAGCAA[C/T]GGGGCTTGTGTTGTC	5253
rs12238477	snp	A/G	0.0689305	0.172377	intron-variant	PHF2	GRCh38.p7	9:93661228	ACCATGAACCCCTGA[A/G]GCACCATTGAGTGTG	5253
rs12238738	snp	A/G	0.318174	0.240525	intron-variant	PHF2	GRCh38.p7	9:93631525	CAAGCTCATTAACCT[A/G]TCATCTGGTTATTGC	5253
rs12335855	snp	C/T	0.16846	0.236329	intron-variant	PHF2	GRCh38.p7	9:93677205	CCTGATCTGCCTGCA[C/T]CCCTGCACCCCAGCC	5253
rs12335919	snp	A/G	0.347032	0.230401	intron-variant	PHF2	GRCh38.p7	9:93662568	TGGATGGATGGATGG[A/G]TGGATGAACAAATGC	5253
rs12339150	snp	A/G	0.369346	0.219673	intron-variant	PHF2	GRCh38.p7	9:93662507	TGGGTGGATGAATGG[A/G]ATGAACGAATGGATG	5253
rs12340447	snp	A/G/T	0.0441095	0.141807	intron-variant	PHF2	GRCh38.p7	9:93596221	GGTTTCCCTGTTTCT[A/G/T]TTGGGACCCCCTGTG	5253
rs12341126	snp	G/T	0.189261	0.242509	intron-variant	PHF2	GRCh38.p7	9:93638895	ggctaattttttgta[G/T]ttttagtagagacag	5253
rs12341865	snp	C/T	0.255503	0.249939	intron-variant	PHF2	GRCh38.p7	9:93642003	ttttgcatatggata[C/T]caacttttcctagca	5253
rs12345288	snp	C/G	0.119978	0.213528	intron-variant	PHF2	GRCh38.p7	9:93584045	gttggtcaggctggt[C/G]tcgaactctcgacct	5253
rs12345357	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93601836	TGATGAGGGTGACAA[A/G]CAATGGGAGGAGGCT	5253
rs12348843	snp	C/T	0.0444908	0.142359	intron-variant	PHF2	GRCh38.p7	9:93592299	CCACTGTGGGAGCAG[C/T]GGGGTGATCCCAGGC	5253
rs12348927	snp	A/G	0.255224	0.249945	intron-variant	PHF2	GRCh38.p7	9:93644960	AGGATGCTCTTGTCC[A/G]GGTCCTTGGGTTGTC	5253
rs12348968	snp	G/T	0	0	intron-variant	PHF2	GRCh38.p7	9:93645069	TGTGGGGACAGGCTA[G/T]GCAGGGCGAGAGAGA	5253
rs12349481	snp	C/T	0.139558	0.224282	intron-variant	PHF2	GRCh38.p7	9:93662513	gatgaatgggatgaa[C/T]gaatggatggatggg	5253
rs12352026	snp	G/T	0.179744	0.239925	intron-variant	PHF2	GRCh38.p7	9:93655335	tcatattttaatgat[G/T]tataaggctcagaat	5253
rs12376195	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93625542	gagtgcagtggcaca[A/G]tctcggctcactgca	5253
rs12551277	snp	A/G	0.00119737	0.0244387	intron-variant	PHF2	GRCh38.p7	9:93655347	gatttataaggctca[A/G]aatcttctgtaatct	5253
rs12551314	snp	A/C	0.231189	0.249291	intron-variant	PHF2	GRCh38.p7	9:93617515	AGAGATCCCAAGAGG[A/C]AATTGTGGGGCCTCT	5253
rs12551694	snp	A/G	0.0759472	0.179459	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666619	AATGTTCATTAGAAG[A/G]GCAGCGGCTCTTTAA	5253
rs12552085	snp	C/G	0.471578	0.115772	intron-variant	PHF2	GRCh38.p7	9:93620447	CTCAGCTCCTGTGAG[C/G]CAGCACTGTCCCCAT	5253
rs12553775	snp	A/C	0.157148	0.232118	intron-variant	PHF2	GRCh38.p7	9:93630107	AGAGAGCAGCATCCA[A/C]CCTGCCTGGGCTGCG	5253
rs12553995	snp	C/T	0.0948562	0.196037	intron-variant	PHF2	GRCh38.p7	9:93620747	AGTATCTTATGCTCC[C/T]GGCTTTAGTGTGAGG	5253
rs12555742	snp	G/T	0.00943375	0.0680285	intron-variant	PHF2	GRCh38.p7	9:93613379	GTGGTCCCTGTAACA[G/T]AAGTTATAGCCCCGA	5253
rs12555927	snp	G/T	0.078151	0.181571	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666800	CCGAGCGAGTGAGCC[G/T]GTAGTCCCAGCTACT	5253
rs12683405	snp	C/G	0	0	intron-variant	PHF2	GRCh38.p7	9:93649512	CCTCTGGTCTTGGCC[C/G]TGCCCATCCCACTCC	5253
rs13284449	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93596759	GCCGTtttttttttt[G/T]gttttttgttttttg	5253
rs13284452	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93596766	tttttttttgttttt[G/T]gttttttgttttgag	5253
rs13286188	snp	A/G	0.393065	0.205018	intron-variant	PHF2	GRCh38.p7	9:93620742	TTCTCAGTATCTTAT[A/G]CTCCTGGCTTTAGTG	5253
rs13286258	snp	A/G			intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593123	aaaagaaaaaaaaaG[A/G]ACTAAGAACAGATGC	5253
rs13287473	snp	A/C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593125	aagaaaaaaaaaGGA[A/C/G]TAAGAACAGATGCTA	5253
rs13288704	snp	A/G	0	0	intron-variant	PHF2	GRCh38.p7	9:93676459	GCCCCTGGCGGCCCA[A/G]AGTCAGGCCTCAGGC	5253
rs13288714	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93676479	AGGCCTCAGGCCCCT[G/T]CTGCCCAGCCCTGCT	5253
rs13288719	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93676492	CTGCTGCCCAGCCCT[G/T]CTGTGCTCAAGGGCC	5253
rs13289575	snp	C/T	0.0364509	0.129988	intron-variant	PHF2	GRCh38.p7	9:93638919	gagacagggtttcac[C/T]atgttggccaggatg	5253
rs13289911	snp	C/G			intron-variant	PHF2	GRCh38.p7	9:93676467	CGGCCCAGAGTCAGG[C/G]CTCAGGCCCCTGCTG	5253
rs13290276	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93618385	CACAGACATGGACAC[A/G]CATACGCATGCATAC	5253
rs13291079	snp	C/T	0.428937	0.17459	intron-variant	PHF2	GRCh38.p7	9:93598368	TCAGGACCTTGGTTC[C/T]CATCCTACCAGAGGA	5253
rs13291161	snp	C/G			intron-variant	PHF2	GRCh38.p7	9:93615362	gatggtgatggtgat[C/G]atggtgatagtaatg	5253
rs13291198	snp	C/G			upstream-variant-2KB	PHF2	GRCh38.p7	9:93576113	GGTCCCGCCCACCTT[C/G]TCCCCGGGGTCCCAC	5253
rs13292190	snp	A/T			intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593074	TCTTTGCTTTTCTTG[A/T]CCTTTATGCCaaaaa	5253
rs13292192	snp	A/T			intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593079	GCTTTTCTTGTCCTT[A/T]ATGCCaaaaaaaaaa	5253
rs13293450	snp	A/G			intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669676	TGCCGGACCCTCAGA[A/G]AGCAGTGGGTTCGGG	5253
rs13294164	snp	G/T	0	0	intron-variant	PHF2	GRCh38.p7	9:93645939	GTACTCTGTTCCCGG[G/T]GCTCTTAGTTCAGAC	5253
rs13294381	snp	A/C	0.345482	0.231048	intron-variant	PHF2	GRCh38.p7	9:93587256	GTGAGGGATGATGGA[A/C]GAGCCCTGGGTGAGG	5253
rs13296436	snp	A/C	0	0	intron-variant	PHF2	GRCh38.p7	9:93625765	ttacaggcatgagtc[A/C]caatacacagtacct	5253
rs13296529	snp	C/T	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93618394	GGACACGCATACGCA[C/T]GCATACACATGGCAA	5253
rs13297695	snp	A/G	0	0	intron-variant	PHF2	GRCh38.p7	9:93652912	GGAGGTTCCCTCTCA[A/G]GGGTAGATGGTTTTG	5253
rs13298406	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93596760	CCGTTTTTTTTTTTT[G/T]TTTTTTGTTTTTTGT	5253
rs13298412	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93596767	ttttttttgtttttt[G/T]ttttttgttttgaga	5253
rs13301391	snp	C/T			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671261	GTGTAGATGCAGGTG[C/T]GGGTGTGGGAGTAGG	5253
rs13301406	snp	C/T			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671285	GAGTAGGCACAGGTG[C/T]AGATGCAGATGTGGG	5253
rs13302803	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93609098	acttttttttagtgg[G/T]tgttttaaaatgtgc	5253
rs13440078	snp	C/T	0.233527	0.249457	intron-variant	PHF2	GRCh38.p7	9:93642411	ttgatttccttctta[C/T]agaattatatctttt	5253
rs13440115	snp	C/T	0.255224	0.249945	intron-variant	PHF2	GRCh38.p7	9:93642891	aaaaaattttgatca[C/T]tgtattttttatttc	5253
rs16912641	snp	A/G	0.0505539	0.150736	synonymous-codon	PHF2	GRCh38.p7	9:93649132	CTGCAAGATGAAGCT[A/G]AAGGAGTTTGTGGAC	5253
rs16912647	snp	A/G	0.0670745	0.170406	intron-variant	PHF2	GRCh38.p7	9:93634206	GAAGGCACTTTGTGA[A/G]CTCTGGAGCCCCTTG	5253
rs17533702	snp	A/T	0.471483	0.115954	intron-variant	PHF2	GRCh38.p7	9:93598946	CCCCACCTTTTGACG[A/T]GGCTGGTATGTCCGT	5253
rs17534161	snp	A/G	0.0596104	0.162024	intron-variant	PHF2	GRCh38.p7	9:93630574	CCTTGCCTTTCCCAC[A/G]CAACCTGCTGTTTGT	5253
rs28380699	snp	C/T	0.0410537	0.137264	utr-variant-3-prime	PHF2	GRCh38.p7	9:93677841	AGCCGGCAGAGCGAG[C/T]CCAGCGTGGCCCCTC	5253
rs28530486	snp	A/G			intron-variant	PHF2, LOC107987098	GRCh38.p7	9:93671472	CAGGTGTAGATGCAG[A/G]TGTGGGTGTGGGAGT	5253
rs28715378	snp	G/T			intron-variant	PHF2, LOC107987098	GRCh38.p7	9:93671441	GTGTAGATGCAGGTG[G/T]GTGTGGATGTAGGTA	5253
rs28729158	snp	A/G			intron-variant	PHF2, LOC107987098	GRCh38.p7	9:93671484	CAGATGTGGGTGTGG[A/G]AGTAGGTACAGGTGT	5253
rs28835702	snp	C/T	0.147321	0.227941	intron-variant	PHF2	GRCh38.p7	9:93625763	GATTACAGGCATGAG[C/T]CACAATACACAGTAC	5253
rs33975810	in-del	-/A/AA	0.42	0.183303	intron-variant	PHF2	GRCh38.p7	9:93608009	GAGAGAGAGAGAGAG[-/A/AA]AAGGAAAGGAGGAAG	5253
rs34012114	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93599987	CCCAGGAACAGCCCC[-/G]GGGGATTCCCCTGGC	5253
rs34020454	in-del	-/A			intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668937	GTATCGGCTGCTTGG[-/A]AAAAAACTGCTGAAG	5253
rs34025557	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93582048	TTAATGCCATAGGGG[-/T]TTTTTCATTCATCAT	5253
rs34033348	in-del	-/T	0.490673	0.0676508	intron-variant	PHF2	GRCh38.p7	9:93640125	TTGCTTGGTCTTTGG[-/T]TTTTTTTTGCAGTTC	5253
rs34091968	in-del	-/T	0.349671	0.229272	intron-variant	PHF2	GRCh38.p7	9:93601460	TAAGAGGGCCTAGTC[-/T]TTTTTTCCCTTCAGT	5253
rs34103739	snp	A/G	0.390651	0.206682	intron-variant, utr-variant-3-prime	PHF2, LOC107987098	GRCh38.p7	9:93673368	AGCCCTCCCTGTGGC[A/G]TATGGGTGGATGAGC	5253
rs34196650	snp	A/G	0.089084	0.191327	intron-variant	PHF2	GRCh38.p7	9:93624690	ATGATGATGATGGTG[A/G]TGGCGATGGTGGTAG	5253
rs34199692	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93634887	TGGCTTTGCCCTGAG[-/A]AAAAGGCCCAGCAGA	5253
rs34279404	snp	A/C	0.137174	0.223093	missense	PHF2	GRCh38.p7	9:93630037	CCAAACTGTGAGAAA[A/C]CCCATGGGAAGTCCA	5253
rs34289742	snp	A/G	0.00316631	0.0396627	synonymous-codon, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666048	GCCAAAGCTGGACTC[A/G]GCAGCGTACAAGGTG	5253
rs34293739	in-del	-/T	0	0	intron-variant	PHF2	GRCh38.p7	9:93596748	TCAGTGTTTCTGCCG[-/T]TTTTTTTTTTTGTTT	5253
rs34351824	in-del	-/C			intron-variant	PHF2	GRCh38.p7	9:93634862	GTGAACAAGCACCTA[-/C]CCGCACCAGGTGGCT	5253
rs34374925	in-del	-/C			intron-variant	PHF2	GRCh38.p7	9:93578026	TCCGGGATTCTCCTT[-/C]CCAGAGAGGAGATCC	5253
rs34389956	in-del	-/T	0.422158	0.181278	intron-variant	PHF2	GRCh38.p7	9:93604839	CTTGAATTCTGAGCC[-/T]TTTTTTTAGCATTTC	5253
rs34392832	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93630155	CTGGGCCTGGGCCCT[-/G]GGGTTGCTGGGGGCA	5253
rs34471538	in-del	-/T	0.392696	0.205275	intron-variant	PHF2	GRCh38.p7	9:93616652	ATGTTTCTCCTATAA[-/T]TTTTTTTTTTTTTCT	5253
rs34525240	in-del	-/T	0.44858	0.151875	intron-variant	PHF2	GRCh38.p7	9:93610072	ATGCCTAGGTGTAGA[-/T]TTTTTTTTGCGGGGA	5253
rs34553705	in-del	-/A	0	0	intron-variant	PHF2	GRCh38.p7	9:93614762	GTCCATTAGCCCAGC[-/A]AAAAAAAAGTGATGA	5253
rs34627691	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93621495	GGTGGGTGGTGCTGG[-/A]AAGGAGGAAGCCCAC	5253
rs34687231	in-del	-/C			intron-variant	PHF2	GRCh38.p7	9:93598726	CCATTTTTCCTCAGT[-/C]CCCCATCCCAGGCTG	5253
rs34690771	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93644760	ATGGGCTGGGGCTGA[-/G]GGCTCTGGGTCCAGC	5253
rs34696009	in-del	-/CTGT	0.496937	0.0390173	intron-variant	PHF2	GRCh38.p7	9:93632939	CACTGTGCCCAGAGG[-/CTGT]CTATGATGCCCCAGT	5253
rs34706891	snp	A/G	0.00119737	0.0244387	intron-variant	PHF2	GRCh38.p7	9:93627329	ATCCAACTGGTTTTT[A/G]TGTGTTGTTTTTGCA	5253
rs34776405	in-del	-/T	0.499974	0.00359416	intron-variant	PHF2	GRCh38.p7	9:93583575	CTAATTTTTTTTTTT[-/T]AAATTAAAGCTATTC	5253
rs34782186	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93636125	TCAGGGCCTGAATGA[-/G]GGAGGGGTCCTGGGA	5253
rs34817076	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93605213	TTTTTGTGTTGTACA[-/T]TTTTTATTTTATACA	5253
rs34837189	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93649877	CATGGACACACTTGT[-/G]CAACACACTCGTGAC	5253
rs34837417	in-del	-/G	0.434398	0.168811	intron-variant	PHF2	GRCh38.p7	9:93612330	TTTACTAATGTGTGT[-/G]TTTTGCCAAGAATAT	5253
rs34848566	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93604054	CATCTCTGCTGAGTT[-/G]GGGCAGAGTCCCAGC	5253
rs34854229	snp	A/G	0.00373275	0.04304	synonymous-codon	PHF2	GRCh38.p7	9:93674979	CTTTAAGTCCCGGTC[A/G]AAGAAAAGGAAAGGC	5253
rs34855444	in-del	-/AG	0.491987	0.0627894	intron-variant	PHF2	GRCh38.p7	9:93650141	AGCACTCACCAACAC[-/AG]GGTACACTCACACAT	5253
rs34900573	in-del	-/C			intron-variant	PHF2	GRCh38.p7	9:93677369	TCCTACCTGCCAGGG[-/C]CCCTTGAGGACACGG	5253
rs34988128	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93649482	ACAAAAATAAGGAGC[-/A]AAAAGGCAAAGCCTC	5253
rs34989156	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93626058	ACCAGCCTGACCAAC[-/A]AAGGTGAAACCCCAT	5253
rs35037748	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93611428	TCAAAAAAAAAAAAA[-/A]GAGTATTCTTTTTAA	5253
rs35057063	in-del	-/C			frameshift-variant	PHF2	GRCh38.p7	9:93636520	CGGAGCCGGACCTTT[-/C]CCCAGGTGGGCTGGC	5253
rs35094322	snp	A/T	0.493613	0.0561475	intron-variant	PHF2	GRCh38.p7	9:93587078	TTCTTTAGTTTGCAG[A/T]CTGTAAAGTTCTCTC	5253
rs35097935	in-del	-/TT			intron-variant	PHF2	GRCh38.p7	9:93608399	GTTTTTTTTTTTTTT[-/TT]CTTGTAATGTGTTTG	5253
rs35107238	in-del	-/C			intron-variant	PHF2	GRCh38.p7	9:93632299	TTGCAGATGGTGGGA[-/C]CCCCCAGCCCCTGCC	5253
rs35137913	snp	G/T	0.372041	0.27558	intron-variant	PHF2	GRCh38.p7	9:93674351	CCTCCACCTAGACCC[G/T]CCAGGCAGGGTGGGG	5253
rs35164841	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93647649	AATCCCAGCACTTTA[G/T]GAGGCTGAGGTGGGT	5253
rs35171420	snp	A/G	0.390464	0.206809	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666767	AACCCCATCTCTACT[A/G]AAAATACAAAAAATT	5253
rs35211530	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93664489	AGGAGGGGCGGCCAC[-/T]TTTTCTGCAGCAGCC	5253
rs35219228	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93656994	CCTTAGGCTCCCTCA[-/G]GGGCCTGGCAACTGG	5253
rs35236745	snp	C/T	0.00296242	0.0383723	missense	PHF2	GRCh38.p7	9:93676934	GGCGGCCCTCCGCAT[C/T]GTCTCCAAACAACAA	5253
rs35363334	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93600812	GCCAGCCTCTCATTC[-/A]AAAGTCTAACCAGGC	5253
rs35458657	in-del	-/AA	0.393987	0.204372	intron-variant	PHF2	GRCh38.p7	9:93661025	AAGACATTGAGGTTG[-/AA]AAACCTGAAGGTAGA	5253
rs35477424	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93599854	TGAAACTCGTCTGAC[-/T]TGGGTGTCCTGTGGT	5253
rs35505758	snp	A/G/T	0.03654	0.130137	synonymous-codon	PHF2	GRCh38.p7	9:93645671	AGGAAGTCAGCTCAC[A/G/T]CTGGGCTACATGGAG	5253
rs35516543	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93583540	TCAGCAACGTTCCAA[-/T]TTTCTCCACATCCTC	5253
rs35537053	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93587103	CTCTCAGAGTTCTGT[-/G]GGGAGGCATGGAGTA	5253
rs35557426	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93643010	CTTCTGAATGTGTTG[-/A]AGTATATTTATTTTC	5253
rs35558040	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93592248	TCCTGGGGGATCCCT[-/G]GGGAAGATAGTTGCC	5253
rs35606186	in-del	-/C			intron-variant	PHF2	GRCh38.p7	9:93648149	TCTCTTTTCTTCTGA[-/C]CAGCCCCATTTCATT	5253
rs35626902	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93625937	CTCCACATCCTCTCC[-/A]AAACTTACTTTAAAA	5253
rs35695657	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93587531	GGAGGAGTCCCAGAT[A/G]GTGGATGGAGGAGCC	5253
rs35700050	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93674271	CTTTTGAGGGTCACA[-/G]GGGTCACCGCCTCAC	5253
rs35746379	in-del	-/A	0.00199481	0.0315187	intron-variant	PHF2	GRCh38.p7	9:93625949	TCCAAAACTTACTTT[-/A]AAAAAAAAATTGGCC	5253
rs35754154	in-del	-/A	0	0	upstream-variant-2KB	PHF2	GRCh38.p7	9:93574951	AAAAAAAAAAAAAAA[-/A]TTCCAGGCTTTCACC	5253
rs35806470	in-del	-/C			intron-variant	PHF2	GRCh38.p7	9:93605517	CCATCCCTCCCAGTA[-/C]CCCCCAAACCTCTGA	5253
rs35872422	in-del	-/AAA			intron-variant	PHF2	GRCh38.p7	9:93647889	ATGAGATTTCATCTC[-/AAA]AAAAAAAAAAAATTC	5253
rs35885717	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93647603	GTATTTTAAAAGGAA[-/T]TTCTGATCAGGCATG	5253
rs35940700	in-del	-/C			intron-variant	PHF2	GRCh38.p7	9:93649065	CTCCTCCCACCACCT[-/C]CCTAGGGCCGGAACG	5253
rs35972560	in-del	-/G			intron-variant	PHF2	GRCh38.p7	9:93588983	TGGTATTTATGTTTA[-/G]GGGAAGTCCCTCTGG	5253
rs36063067	in-del	-/C			utr-variant-3-prime	PHF2	GRCh38.p7	9:93679263	TTGGAGGGACGCAGT[-/C]CCTAGGGCCCGAGAC	5253
rs36083667	in-del	-/TT			intron-variant	PHF2	GRCh38.p7	9:93607461	AACATGCCTGGCTAA[-/TT]TTTTTTTTTTTTTTT	5253
rs36099518	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93628647	AGCTTCCATTCCAGG[-/T]AGCTTGCTGCCCTGA	5253
rs36106927	in-del	-/C			intron-variant	PHF2	GRCh38.p7	9:93660771	CCTGCAGCATCCAGG[-/C]CCCAGACCCCCCCAG	5253
rs41274426	snp	C/T	0.00159617	0.0282053	intron-variant	PHF2	GRCh38.p7	9:93630121	ACCCTGCCTGGGCTG[C/T]GTGGAGGGTGAGGTC	5253
rs41274432	snp	C/G	0.0256215	0.110247	intron-variant	PHF2	GRCh38.p7	9:93654355	TAGGACCTGTCACTT[C/G]CACCCCCGACCCCCG	5253
rs41276188	snp	C/G	0.000920357	0.021432	intron-variant	PHF2	GRCh38.p7	9:93658104	GAAGGCACCTGTGGG[C/G]AGCAGGCACCCACCC	5253
rs41276190	snp	C/T			missense	PHF2	GRCh38.p7	9:93658177	AAGCAGCTGCCCCCT[C/T]ATCTAGTCCAAGGAG	5253
rs41276198	snp	C/T	0.220895	0.2483	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93665961	CCCCGCAAGGCCTCC[C/T]GCTGGACTGCCATCT	5253
rs41276200	snp	A/G	0.02177	0.102035	missense, downstream-variant-500B	PHF2, LOC107987098	GRCh38.p7	9:93673755	GTGGCAGTGGCAAGA[A/G]TGCAGGCAAACGACT	5253
rs41276202	snp	C/T	0.0498117	0.149749	intron-variant	PHF2	GRCh38.p7	9:93677197	GCTCAGCCCCTGATC[C/T]GCCTGCACCCCTGCA	5253
rs41276204	snp	A/C	0.168785	0.236441	utr-variant-3-prime	PHF2	GRCh38.p7	9:93677769	GCCGAGCTGCCTCAC[A/C]AGGGAGGGCCTTGCC	5253
rs41297181	snp	A/G	0.0779096	0.181342	synonymous-codon, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93667157	TGCCAGAGTCAAGAA[A/G]GAGAGTGGGAGCTCG	5253
rs41305607	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93649246	GGGGTGTGGGGGCTG[A/G]GGTTGGGGCAGGGGC	5253
rs41306463	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93649241	CCCTGGGGGTGTGGG[A/G]GCTGGGGTTGGGGCA	5253
rs55647503	in-del	-/T	0.455502	0.142369	intron-variant	PHF2	GRCh38.p7	9:93627493	CCTTTTATTTCAGGA[-/T]TTTTTTTTTTTTTTT	5253
rs55688959	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672336	CAGGTGTAGATGCAG[A/G]TGTGGGTGTGGGAGT	5253
rs55693105	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672096	CAGGTGTGGGTGTGG[A/G]TGTAGGTACAGGTGT	5253
rs55698495	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672228	CAGGTGTAGATGCAG[A/G]TGTGGGTGTGGATGT	5253
rs55712092	snp	A/T			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672032	GGTGTGGGAGTAGGC[A/T]CAGGTGTAGATGCAG	5253
rs55714459	snp	C/T	0.497829	0.0328757	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672129	ATGCAGGTGTGGGTG[C/T]GGATGTAGGTACAGG	5253
rs55725031	in-del	-/GGT/TGG	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93648118	CCCCACATTGCATTT[-/GGT/TGG]TTTTATATCCCTGAA	5253
rs55728607	snp	A/T			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93672349	AGATGTGGGTGTGGG[A/T]GTAGGGTCAGGTGTA	5253
rs55742090	snp	A/T			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672097	AGGTGTGGGTGTGGA[A/T]GTAGGTACAGGTGTA	5253
rs55742666	snp	C/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618911	TGTGTGTATGTGCGT[C/G]TGCATGTGTGGTGTG	5253
rs55748036	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666297	CACTGAGCCTCCTGC[C/T]GGGGGAGGTTATTGG	5253
rs55780766	snp	C/T			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93672247	GGGTGTGGATGTAGG[C/T]ACAGGTGTAGATGCA	5253
rs55783363	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672204	CAGATGTGGGTGTGG[A/G]AGTAGGCACAGGTGT	5253
rs55783552	snp	C/G	0.0770498	0.180522	intron-variant	PHF2	GRCh38.p7	9:93637205	CCAACTCCCTTCTTG[C/G]ATGTGTGATTTCTAA	5253
rs55794025	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672348	CAGATGTGGGTGTGG[A/G]AGTAGGGTCAGGTGT	5253
rs55813150	snp	A/T			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672241	AGGTGTGGGTGTGGA[A/T]GTAGGTACAGGTGTA	5253
rs55820920	snp	A/T	0.000798403	0.0199641	intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93672205	AGATGTGGGTGTGGG[A/T]GTAGGCACAGGTGTA	5253
rs55846473	snp	C/T	0.177824	0.239355	intron-variant	PHF2	GRCh38.p7	9:93622269	GGCCCAGCCAGCCTG[C/T]CCATACACCGAGCCT	5253
rs55851551	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618917	TATGTGCGTCTGCAT[A/G]TGTGGTGTGTGAGTT	5253
rs55858603	snp	C/G			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93672391	GAGTGTGGGAGTAGG[C/G]ACAGGTGCAGGTGCA	5253
rs55880829	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672240	CAGGTGTGGGTGTGG[A/G]TGTAGGTACAGGTGT	5253
rs55886707	snp	A/G	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672377	GTAGATGCAGGTGTG[A/G]GTGTGGGAGTAGGCA	5253
rs55915414	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672192	CAGGTGTAGATGCAG[A/G]TGTGGGTGTGGGAGT	5253
rs55934002	snp	C/T	0.161924	0.233971	intron-variant	PHF2	GRCh38.p7	9:93607142	TCATGGAGTGTCAGT[C/T]CTCTGACTTTGTTTT	5253
rs55980031	snp	C/T			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93672211	GGGTGTGGGAGTAGG[C/T]ACAGGTGTAGATGCA	5253
rs56005625	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618924	GTCTGCATGTGTGGT[A/G]TGTGAGTTTGTATGT	5253
rs56007726	snp	C/T			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93672067	GGGTGTGGGAGTAGG[C/T]ACAGGTGTAGATGCA	5253
rs56116015	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672372	CAGGTGTAGATGCAG[A/G]TGTGAGTGTGGGAGT	5253
rs56134753	snp	A/T	0.0393456	0.134628	synonymous-codon	PHF2	GRCh38.p7	9:93653200	CAGCTTCGTGGAGCC[A/T]CCTGACATTGTAAAG	5253
rs56186220	snp	C/T	0.0952156	0.196321	intron-variant	PHF2	GRCh38.p7	9:93626000	ATAATCCCAGCACTT[C/T]GGGAGGCCAAGGTGG	5253
rs56188181	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672048	CAGGTGTAGATGCAG[A/G]TGTGGGTGTGGGAGT	5253
rs56211322	snp	G/T			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93672355	GGGTGTGGGAGTAGG[G/T]TCAGGTGTAGATGCA	5253
rs56230134	snp	A/T			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672356	GGTGTGGGAGTAGGG[A/T]CAGGTGTAGATGCAG	5253
rs56259948	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672413	GCAGGTGCAGGTGTG[A/G]GTGTGGGAGTAGGCA	5253
rs56274752	snp	C/T	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672399	GAGTAGGCACAGGTG[C/T]AGGTGCAGGTGTGGG	5253
rs56301302	snp	C/G			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93672031	GGGTGTGGGAGTAGG[C/G]ACAGGTGTAGATGCA	5253
rs56309322	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93618936	GGTGTGTGAGTTTGT[A/G]TGTGTGCTAAGCCAG	5253
rs56310424	snp	C/G	0.0759472	0.179459	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666313	GGGGGAGGTTATTGG[C/G]ATCTAGTGTATTAAC	5253
rs56338151	snp	C/T	0.375	0.216506	intron-variant	PHF2	GRCh38.p7	9:93618908	GTGTGTGTGTATGTG[C/T]GTCTGCATGTGTGGT	5253
rs56346644	snp	A/T			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672392	AGTGTGGGAGTAGGC[A/T]CAGGTGCAGGTGCAG	5253
rs56351334	snp	A/G	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93618637	CAATATATTTTTGGT[A/G]TCTTACCATGTCAGT	5253
rs56367805	snp	A/G			intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671954	GATGTGGGTGTGGGA[A/G]TAGGGTCAGGTGTAG	5253
rs56390720	snp	C/T			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93671623	AGATGCAGGTGTGGG[C/T]GTGGATGTAGGTACA	5253
rs56951431	in-del	-/ACAC/CACA	0.375	0.216506	intron-variant	PHF2	GRCh38.p7	9:93663768	GCATCTCACACACAC[-/ACAC/CACA]CACACACTGCATCAC	5253
rs57326662	snp	C/T	0.146985	0.227789	intron-variant	PHF2	GRCh38.p7	9:93634154	CCCATGGAGTAGATA[C/T]AACTGCCTCCATTTC	5253
rs57508871	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93647933	TTTTACCCATAAAAA[-/A]TTCTAGTACATAGCT	5253
rs57570125	snp	A/C			intron-variant	PHF2	GRCh38.p7	9:93674325	GCCACAGGTCATGCC[A/C]TACAGTGTCCCCTCC	5253
rs57580281	snp	C/T	0.0310518	0.120672	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93594691	CACATTGGGACCTTG[C/T]GCCTAAAACATGTGG	5253
rs57656509	in-del	-/CC	0	0	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93594196	ATGTGACCCCCCCCC[-/CC]TCCATTAATGCACAA	5253
rs57658553	snp	A/T	0.221439	0.248363	intron-variant	PHF2	GRCh38.p7	9:93583587	CTAATTTTTTTTTTT[A/T]AATTAAAGCTATTCT	5253
rs57714051	snp	C/T	0.0425829	0.139564	intron-variant	PHF2	GRCh38.p7	9:93585673	CTGATACACCCACCC[C/T]TGGGGCTGCCAGACT	5253
rs57911753	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93588677	CAGGCGGATCACAAG[A/G]TCAGGAGTTCGAGAC	5253
rs57966353	in-del	-/TTTTTTTTT			intron-variant	PHF2	GRCh38.p7	9:93627508	TTTTTTTTTTTTTTT[-/TTTTTTTTT]GTCTAATTGCTCTGG	5253
rs58124920	snp	G/T	0.00835141	0.0640778	intron-variant	PHF2	GRCh38.p7	9:93652944	GGCCTTCTCATTATC[G/T]TCTGGGGGTGGAGGC	5253
rs58301035	snp	A/G/T	0.0592355	0.161582	intron-variant	PHF2	GRCh38.p7	9:93602204	GTATGTAAATTGTTC[A/G/T]TTGAGTTTTGCATTT	5253
rs58782393	snp	G/T	0.161267	0.233723	intron-variant	PHF2	GRCh38.p7	9:93589371	TGGGCTGGAGAATTC[G/T]TTGTGTAGGGGCTTT	5253
rs58925215	snp	A/G	0.105214	0.203807	intron-variant	PHF2	GRCh38.p7	9:93613664	TCCTGGGCTCAAGCA[A/G]GGAACTCCTTGATCC	5253
rs59044538	snp	C/G	0.0256215	0.110247	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93670846	GGAGGATGCGGATGC[C/G]AGACAGGCTGGGCGC	5253
rs59174058	snp	A/G	0.029116	0.117091	intron-variant	PHF2	GRCh38.p7	9:93633467	GACTTTCCTCATCCC[A/G]CCCTGCCCTGTGGGG	5253
rs59257911	snp	G/T	0.0341408	0.126114	intron-variant	PHF2	GRCh38.p7	9:93651987	AGTGGGTATGAATGG[G/T]GGCAATGAGGACTCC	5253
rs59324530	in-del	-/CAGATG			intron-variant, cds-indel	PHF2, LOC107987098	GRCh38.p7	9:93671291	GCACAGGTGCAGATG[-/CAGATG]TGGGTGTGGGAGTAG	5253
rs59436086	snp	A/G	0.0341408	0.126114	intron-variant	PHF2	GRCh38.p7	9:93677116	TGGTCCAAGTTGGTT[A/G]CATCTTTGTGTGAGC	5253
rs59504471	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93651099	TTATTTTAAAAATTA[-/A]AAAAAAAAAAAAAAA	5253
rs59597511	snp	G/T	0.283421	0.247756	intron-variant	PHF2	GRCh38.p7	9:93633936	TCTCCCAGCTGCAAT[G/T]TCACTGCTGCTGCAT	5253
rs59624778	in-del	-/TGG	0.470908	0.117046	intron-variant	PHF2	GRCh38.p7	9:93624684	TGATGATGGTGGTGG[-/TGG]CGATGGTGGTAGAGG	5253
rs59669021	snp	A/G	0.000399281	0.0141238	intron-variant	PHF2	GRCh38.p7	9:93633148	CAGGGTTCCCAGAGC[A/G]AGCTGTGCCTGAGGT	5253
rs59932250	snp	A/C/G	0.0318376	0.122163	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93594719	TGGATTGCAAGGTAC[A/C/G]TGGGGGTTTGACAGA	5253
rs60016166	snp	G/T	0.0256215	0.110247	intron-variant	PHF2	GRCh38.p7	9:93653697	CCAGCCATAGCCAGG[G/T]CCCCGCACAGGAGCC	5253
rs60166120	in-del	-/CC/CCTTTA/CCTTTT	0.625	0.125	intron-variant	PHF2	GRCh38.p7	9:93649380	ATTTTTTCCTTTTTT[-/CC/CCTTTA/CCTTTT]TTTTTTTTTTTTTTT	5253
rs60423599	snp	A/G	0.0399052	0.1355	intron-variant	PHF2	GRCh38.p7	9:93601207	CCATCTACTGAAACC[A/G]TGCAGATTGGCCGGG	5253
rs60471694	snp	A/G	0.0314385	0.121371	intron-variant	PHF2	GRCh38.p7	9:93585740	CAATTCCAGATCACT[A/G]AGATCTTATTGTAGC	5253
rs60483413	snp	A/C			intron-variant	PHF2	GRCh38.p7	9:93612233	CTGCTGCAGTGAATA[A/C]ACATGATCCACGTAT	5253
rs60513643	snp	A/G	0.00914312	0.0669923	intron-variant	PHF2	GRCh38.p7	9:93599193	CAGGGGCTCTCCAGG[A/G]TGGGTTCCGAAGAAG	5253
rs60697416	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93607462	TTTTTTTTTTTTTTT[-/T]GGTAGGGAGAGGGTT	5253
rs60700162	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93650226	ATGACATAGACATGC[A/G]ATACACCCACGGGCA	5253
rs60881410	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93628732	TTACTGGTCAGTTTT[-/T]ATTTACATGCATTTG	5253
rs60993356	snp	A/T	0.0314385	0.121371	intron-variant	PHF2	GRCh38.p7	9:93585741	AATTCCAGATCACTG[A/T]GATCTTATTGTAGCT	5253
rs61301026	snp	A/G	0.0509478	0.151255	intron-variant	PHF2	GRCh38.p7	9:93650175	CACACTCGCCAACAC[A/G]CCTGTGACACGTTCA	5253
rs61403867	snp	A/G	0.499839	0.00898417	intron-variant	PHF2	GRCh38.p7	9:93620839	CTGAATAATTTCTTA[A/G]GGGGCATTTAGAAAG	5253
rs61453782	snp	A/G	0.463989	0.129263	intron-variant	PHF2	GRCh38.p7	9:93624478	TGATGATGGTGTGGC[A/G]GTGATGGTGATGGTG	5253
rs61471428	snp	A/G	0.495368	0.0478996	intron-variant	PHF2	GRCh38.p7	9:93620624	GTTGGTTTTTTGTTA[A/G]TGAGAAGCTTGTGCT	5253
rs61636268	snp	C/G	0.0425829	0.139564	intron-variant	PHF2	GRCh38.p7	9:93579090	CGTCAGGGGTTGGTG[C/G]TGTTGGTACAGCTCT	5253
rs61705936	in-del	-/TCT			intron-variant	PHF2	GRCh38.p7	9:93613545	GGAGATTGGGGTTCT[-/TCT]GATTTTCTTTTTCTT	5253
rs62573983	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93614850	GGTGATGGTGATAGT[A/G]ATGATGATGGTGATG	5253
rs62573984	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93614854	ATGGTGATAGTAATG[A/G]TGATGGTGATGATGG	5253
rs62573985	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93614862	AGTAATGATGATGGT[A/G]ATGATGGTGACAGTG	5253
rs62573986	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93614873	TGGTGATGATGGTGA[C/T]AGTGATGGTGATGGT	5253
rs62573987	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93614880	GATGGTGACAGTGAT[A/G]GTGATGGTGATGGTA	5253
rs62573988	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93614895	GGTGATGGTGATGGT[A/G]ATGATGGTGATGATG	5253
rs62573989	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93614916	GGTGATGATGGTGAT[A/G]GTAATGGTGATGGTG	5253
rs62573990	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93614923	ATGGTGATAGTAATG[A/G]TGATGGTGATGATGG	5253
rs62573991	snp	C/T	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93615453	CTATCTTTACAGCCA[C/T]CAGCTATGTGCCAGG	5253
rs62573992	snp	C/T	0.288906	0.246954	intron-variant	PHF2	GRCh38.p7	9:93619375	GAGGGCCTGATTCGG[C/T]GTCCTGGGCTGGCAT	5253
rs62573993	snp	C/G	0.450483	0.149354	intron-variant	PHF2	GRCh38.p7	9:93622804	TTGTCCCCAGAACAG[C/G]CATGTTCCAGGGAGT	5253
rs62573996	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93646053	GGAGACCCTTTGATT[C/T]TGGCAGCTATGAATT	5253
rs62573997	snp	A/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93647902	TCAAAAAAAAAAAAT[A/T]CTTTTTATATACATC	5253
rs62573998	snp	C/G	0.0360663	0.129354	intron-variant	PHF2	GRCh38.p7	9:93674205	GGCATTCCTCGACAG[C/G]CCCCGGAGGTTGAAG	5253
rs62574554	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93581404	TAGAACCTCAAATGC[C/T]GGGGAGTACTGGGGG	5253
rs62574555	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93587063	GGACAAGGCACAACA[G/T]TCTTTAGTTTGCAGT	5253
rs62574557	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93597032	GCCTCCCCAGTTCAT[G/T]CCATTCTCCAGCCTC	5253
rs62574558	snp	G/T	0.470715	0.117409	intron-variant	PHF2	GRCh38.p7	9:93600380	CCAGAGCTGCGTCTT[G/T]GTGATCTCCCAGTCC	5253
rs62574559	snp	A/G	0.0103295	0.0711199	intron-variant	PHF2	GRCh38.p7	9:93603851	TGGCATCCCCATAGG[A/G]TTCTGTGTGCCCTGA	5253
rs66957358	in-del	-/AG			intron-variant	PHF2	GRCh38.p7	9:93650142	GCACTCACCAACACG[-/AG]GTACACTCACACATG	5253
rs67001312	in-del	-/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93602270	TTTTTTTTTTTTTTT[-/T]TTTGAGATGGAATCT	5253
rs68180235	in-del	-/TGCAGA	0.359787	0.224604	intron-variant, cds-indel	PHF2, LOC107987098	GRCh38.p7	9:93671283	GGGAGTAGGCACAGG[-/TGCAGA]TGCAGATGTGGGTGT	5253
rs71364385	in-del	-/GGAAAA	0	0	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93593109	AAAAAAAAAAAAAAA[-/GGAAAA]AAGAAAAAAAAAGGA	5253
rs71364388	in-del	-/A/AA	0.488606	0.0746142	intron-variant	PHF2	GRCh38.p7	9:93655276	TTTAAAATGAAAAAA[-/A/AA]AAAAAAAACCAACCC	5253
rs71496443	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93580002	GGGGAGGGAGAATCG[G/T]TGTGTTCTATCCTTG	5253
rs71496444	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93600240	CATGGGGGGTGTGTG[A/G]ATGTGTGTCTGTGTG	5253
rs71496445	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93620297	CCCACTTCCCCACAT[C/T]TGGGTCCTCATGGAG	5253
rs71496446	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93647558	GCTTTCAGCCAGTTT[C/T]CCGTTTCCCCACTTT	5253
rs71496447	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93651838	GTGTGGTGGGAGGCA[A/G]GGACAGCCTGGCCCC	5253
rs71499165	in-del	AGATTGGGGTTC/GGATTGGGG	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93613532	AGTAGGTCCCGGTGG[AGATTGGGGTTC/GGATTGGGG]TTCTGATTTTCTTTT	5253
rs71511669	in-del	-/AA/AAA	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93647900	CTCAAAAAAAAAAAA[-/AA/AAA]TTCTTTTTATATACA	5253
rs71511670	in-del	-/TTTT	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93649398	TTTTTTTTTTTTTTT[-/TTTT]ATAAGACTGGCCCAC	5253
rs71511671	multinucleotide-polymorphism	AT/GA	0.5	0	intron-variant, frameshift-variant	PHF2, LOC107987098	GRCh38.p7	9:93672205	CAGGTGTGGGTGTGG[AT/GA]GTAGGTACAGGTGTA	5253
rs72150120	in-del	-/CACT	0.0785177	0.181917	intron-variant	PHF2	GRCh38.p7	9:93650008	CACGTGGTACACTCA[-/CACT]CACGGACACACTCGC	5253
rs72466629	snp	G/T	0.375	0.216506	intron-variant	PHF2	GRCh38.p7	9:93617891	GGCAGCTGATTAGAT[G/T]GTGCCCACCGAGATT	5253
rs72546545	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93640132	GTCTTTGGTTTTTTT[-/T]TGCAGTTCAAATATG	5253
rs72546547	in-del	-/AG			intron-variant	PHF2	GRCh38.p7	9:93650140	TAGCACTCACCAACA[-/AG]CGGTACACTCACACA	5253
rs72745445	snp	C/T	0.00597247	0.0543191	intron-variant	PHF2	GRCh38.p7	9:93587770	GGGACAGTGTTGTTA[C/T]GTGACTCTCATGATC	5253
rs72745477	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93611033	GCCTCAAGTTCTTGC[C/T]TGCTTCTAGCAACTT	5253
rs72745479	snp	A/C	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93611918	AGAAGCTTGCCCTCT[A/C]TCCCTGCTGAGCACA	5253
rs72745480	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93613222	TATATTCTAGAAATG[C/T]AGTTGAGAAGTGAAT	5253
rs72745481	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93613227	TCTAGAAATGTAGTT[A/G]AGAAGTGAATTCCCT	5253
rs72745485	snp	A/T			intron-variant	PHF2	GRCh38.p7	9:93614207	ACAAATTGAGAAGTT[A/T]AAGCAGCACAGGCTC	5253
rs72745487	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93614439	TCCCTCTGGCTGCCC[C/T]TCCTGCTGAAGAGAA	5253
rs72745490	snp	A/T	0.133435	0.221162	intron-variant	PHF2	GRCh38.p7	9:93616129	CAACCCATTGTTTAA[A/T]GGCTGTGTAATACTC	5253
rs72745492	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93617117	GCATGGTCGGAGGGT[G/T]TCTGAGCCAGGGGCC	5253
rs72745495	snp	C/G			intron-variant	PHF2	GRCh38.p7	9:93621499	GGGTGGTGCTGGAAG[C/G]AGGAAGCCCACAAGG	5253
rs72745496	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93622811	CAGAACAGGCATGTT[C/T]CAGGGAGTGCTGGCC	5253
rs72745500	snp	C/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623842	GCTTCATGCTCTGTT[C/G]CCAGAACTCAAGACT	5253
rs72745501	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93623843	CTTCATGCTCTGTTC[C/T]CAGAACTCAAGACTG	5253
rs72745502	snp	A/C			intron-variant	PHF2	GRCh38.p7	9:93624083	GAGACTATTCTGTGT[A/C]TGGGCAGGCACTTAA	5253
rs72747407	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93625030	ATTCAGTGGTACTTA[A/G]TAAATTCACAATGCT	5253
rs72747414	snp	A/G	0.140581	0.224783	intron-variant	PHF2	GRCh38.p7	9:93633400	ATAGTGGTTAGAAGC[A/G]GCCCTGAATTGCAGC	5253
rs72747426	snp	A/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93651099	TTTATTTTAAAAATT[A/T]AAAAAAAAAAAAAAA	5253
rs72747427	snp	C/T	0.0633504	0.166319	intron-variant	PHF2	GRCh38.p7	9:93651312	GTCTAGGCTATGGAG[C/T]TAGGGAGAGATGGTA	5253
rs72747430	snp	A/G	0.168135	0.236216	intron-variant	PHF2	GRCh38.p7	9:93661326	GGGGTGTAGTGGGAC[A/G]CTTTTGTGTTCTCTT	5253
rs72747444	snp	A/G	5.02567e-05	0.00501257	missense, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93667138	ACACCAAGCCCGGCC[A/G]CAATGCCAGAGTCAA	5253
rs72747446	snp	A/G	0.139225	0.224118	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668133	ATATTACTATTTTAC[A/G]TGCAATATTATGTTC	5253
rs72747448	snp	A/T	0.167484	0.23599	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668160	GTTCATGTAATATTG[A/T]TCAGAAAGCCAGCTG	5253
rs72747451	snp	A/G	0.167809	0.236103	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669068	AGTATTATTTTCCAT[A/G]CCGACTAGTTAGACG	5253
rs73518053	snp	A/G	0.00795532	0.062565	intron-variant	PHF2	GRCh38.p7	9:93592152	CCAGGGGCTCTCAGT[A/G]TGCACCTCCCAGGAG	5253
rs73518058	snp	C/T	0.0360663	0.129354	intron-variant	PHF2	GRCh38.p7	9:93619296	TGGAAACACTGCTCT[C/T]GTTGGAGCCCATCTC	5253
rs73518060	snp	A/G	0.239902	0.249796	intron-variant	PHF2	GRCh38.p7	9:93619513	ATGCGGGCCTTCACC[A/G]GGCTGGTGCTCAGAT	5253
rs73522232	snp	C/G	0.0711525	0.174681	intron-variant	PHF2	GRCh38.p7	9:93620416	GAGTGGGCCTGGCTG[C/G]GGGATCCTTTGTGAG	5253
rs73522240	snp	C/T	0.0399052	0.1355	intron-variant	PHF2	GRCh38.p7	9:93621669	TTTGTGCCTCTGAGT[C/T]CTTGTGCTGGCCGTG	5253
rs73522243	snp	A/G	0.0520825	0.152737	intron-variant	PHF2	GRCh38.p7	9:93621989	GTTCATTGGGGACGT[A/G]CCCAACCACCTGGGG	5253
rs73522245	snp	C/G			intron-variant	PHF2	GRCh38.p7	9:93624233	AGAGTGAGTGCTCAG[C/G]CAGAGTTAGTGATGA	5253
rs73522247	snp	C/T	0.217851	0.247924	intron-variant	PHF2	GRCh38.p7	9:93625249	AGTCCTCATGTGTCA[C/T]GCTTCTTTCATTTAG	5253
rs73522252	snp	C/T	0.0402882	0.136092	intron-variant	PHF2	GRCh38.p7	9:93626421	TACCTGTTTATTAAT[C/T]GGATTGTTTGTCTTT	5253
rs73522271	snp	A/G	0.0345262	0.126772	intron-variant	PHF2	GRCh38.p7	9:93637791	TGGACATATGCTTTT[A/G]TTGTTTTAGGAGTGG	5253
rs73522273	snp	A/G	0.0260105	0.111035	intron-variant	PHF2	GRCh38.p7	9:93639145	AAGTAATTGCTTTCA[A/G]TCTGTAGATCACTCT	5253
rs73522278	snp	C/T	0.00119737	0.0244387	intron-variant	PHF2	GRCh38.p7	9:93642969	TTTTTAATACATCCC[C/T]GTGCCTTGCCGCATC	5253
rs73522292	snp	C/G	0.0345262	0.126772	intron-variant	PHF2	GRCh38.p7	9:93648094	TTTGGCTGTGGAATC[C/G]AAATTAGACCCCCAC	5253
rs73522296	snp	A/G	0.0256215	0.110247	intron-variant	PHF2	GRCh38.p7	9:93651516	TTAAGTCTGTCCCCA[A/G]GGATGTTGGCCAAGC	5253
rs73523904	snp	C/T	0.0260105	0.111035	intron-variant	PHF2	GRCh38.p7	9:93656085	TCCCTCTAGCTGGGT[C/T]GGTGCTAGATGCCTT	5253
rs73523906	snp	A/G	0.0256215	0.110247	intron-variant	PHF2	GRCh38.p7	9:93660046	GTGTGAGTGTGTCAC[A/G]TGATGGTGTGGGGTA	5253
rs73523907	snp	C/T	0.0432317	0.140524	synonymous-codon	PHF2	GRCh38.p7	9:93660506	CAACCTGGACCTGCT[C/T]GAAGCCCACACCAAG	5253
rs73523908	snp	C/T	0.0283406	0.115616	intron-variant	PHF2	GRCh38.p7	9:93661456	GAATGGATGAACAGA[C/T]GGATGGATGAATGAA	5253
rs73523910	snp	C/T	0.0256215	0.110247	intron-variant	PHF2	GRCh38.p7	9:93663170	GTGCTGTGGGGTGTG[C/T]TTACGTGGGTCTGAG	5253
rs73523915	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666493	TGCACAGTGTGAAGA[C/T]AGTTTGGTCCTTTGT	5253
rs73523917	snp	A/G	0.0256215	0.110247	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93667697	AGATGGGGAAACCGA[A/G]GCTCTGAGGGCTTAT	5253
rs73523922	snp	C/G	0.0256215	0.110247	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669042	TTGAGTATGATAATT[C/G]GTGGATTAAAAGTAT	5253
rs73523932	snp	G/T	0.0256215	0.110247	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672492	TGGGAGTAGGCACAG[G/T]TGTACATGCAGGTAT	5253
rs73523933	snp	C/T	0.0271762	0.113356	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93673085	GGAGGGAGTGGGCTA[C/T]GCTGCCCCATCTCAG	5253
rs73523934	snp	C/T	0.0256215	0.110247	intron-variant	PHF2	GRCh38.p7	9:93674164	CACCGGGCGCCATCT[C/T]GCTTCCTCCTGAACC	5253
rs73523942	snp	A/T	0.0256215	0.110247	intron-variant	PHF2	GRCh38.p7	9:93675404	TGGGGTGAGGCCTTG[A/T]CCACCTTCCACATTA	5253
rs73523944	snp	C/T	0.0252325	0.109451	utr-variant-3-prime	PHF2	GRCh38.p7	9:93679501	TTATTTCCCAATTCA[C/T]ATTACTCTTGTATCG	5253
rs73651269	snp	C/T	0.104149	0.203046	intron-variant	PHF2	GRCh38.p7	9:93590015	GGTGTTGCTCCCTGG[C/T]TATCCTGGTCTGTAT	5253
rs73651270	snp	C/T	0.104149	0.203046	intron-variant	PHF2	GRCh38.p7	9:93590123	TTCGGATTTTAAAAT[C/T]GTCAGATTGGTTGTA	5253
rs73651271	snp	A/G	0.290977	0.246619	intron-variant	PHF2	GRCh38.p7	9:93592591	TGGTGAGTCTCTGTC[A/G]CTCAGTGTTCAGAGG	5253
rs73651272	snp	A/G	0.0119091	0.0762411	intron-variant	PHF2	GRCh38.p7	9:93601174	TTTGTGTTCAAGAGT[A/G]TACAGAGCTTTGCAT	5253
rs73651290	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93612112	TGAACAATATACATC[C/T]TGGAAATTGTTCCAG	5253
rs73651291	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93612481	TCTTACTACAAGTGA[C/T]ATTGCACAGCTTCTC	5253
rs73651292	snp	A/G	0.000399281	0.0141238	intron-variant	PHF2	GRCh38.p7	9:93612670	GTTTCCTTTAGGTAC[A/G]TATGACTCATTTGCA	5253
rs73651293	snp	A/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93613046	TCCTGGTCACAGAGC[A/T]TTAGCTGTCTGGGGC	5253
rs73651296	snp	C/G	0.0410537	0.137264	intron-variant	PHF2	GRCh38.p7	9:93616551	ACCCTGTGCCAGATG[C/G]TGCAGAGGGCGGCAA	5253
rs73651297	snp	A/G	0.128976	0.218754	intron-variant	PHF2	GRCh38.p7	9:93620479	GGCGACAACCTTTGA[A/G]GTCAGCAAGATGTGG	5253
rs73651298	snp	A/G	0.105214	0.203807	intron-variant	PHF2	GRCh38.p7	9:93620585	ATCTGGGAATTGCCC[A/G]CTCTGCATTAGTGAG	5253
rs73651299	snp	C/T	0.0356815	0.128715	intron-variant	PHF2	GRCh38.p7	9:93623328	CAGTTCATCTGGTCC[C/T]ACAAAAGTCTTTGCA	5253
rs74312821	in-del	-/AA	0.470811	0.117228	intron-variant	PHF2	GRCh38.p7	9:93616610	TCACCTCTGGGAGTG[-/AA]AGAGGCCACTTCTTT	5253
rs74360278	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93623441	GTCCTGCCCTCCTCT[G/T]TGCTGAGCTCTTCTT	5253
rs74364326	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93586752	GTCCATCTAGCTGGT[G/T]ACGTTTCCTGAACAC	5253
rs74369348	snp	A/G	0.0759472	0.179459	intron-variant	PHF2	GRCh38.p7	9:93664902	AGAGCATTGGAAGCC[A/G]CCTCACCTAGGCACT	5253
rs74387557	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93625144	CCTCTCTCCTCCCAC[C/T]CTCTGGCACCACTAG	5253
rs74409488	snp	C/T	0.0123036	0.0774623	intron-variant	PHF2	GRCh38.p7	9:93586879	GCCCTCATCACCAGC[C/T]GCCTGCGAGTCTGTG	5253
rs74412472	snp	A/G	0.000399281	0.0141238	intron-variant	PHF2	GRCh38.p7	9:93604913	TTAGCATTCCCACCC[A/G]TGACCACTGATGACC	5253
rs74421510	snp	A/G	0.077417	0.180873	intron-variant	PHF2	GRCh38.p7	9:93634872	CACCTACCGCACCAG[A/G]TGGCTTTGCCCTGAG	5253
rs74429411	snp	A/G	0.00835141	0.0640778	intron-variant	PHF2	GRCh38.p7	9:93597819	ACAGTGTTGGGAAGT[A/G]TCTTATAGCCAAGAT	5253
rs74541871	snp	C/T	0.0399052	0.1355	intron-variant	PHF2	GRCh38.p7	9:93656797	CTGGGCCTCTCCTTC[C/T]GATTGGACTGTCCCT	5253
rs74546246	in-del	-/A			intron-variant	PHF2	GRCh38.p7	9:93618897	ATATGTTTGTGTGTG[-/A]TGTGTATGTGCGTCT	5253
rs74558925	snp	C/T	0.00159617	0.0282053	intron-variant	PHF2	GRCh38.p7	9:93660090	GGGCTGATAGTTCCC[C/T]GCCAGCCTGGCACTG	5253
rs74579791	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93611882	GGAAAATATTCAATA[A/G]TAAAAAATTTGTCTC	5253
rs74604187	snp	A/C	0.0158469	0.0875917	intron-variant	PHF2	GRCh38.p7	9:93581066	CAGAAGGTAGAGTGG[A/C]CAAGACTTGCCTGGC	5253
rs74613580	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93625103	CCAAAGGAAACTCCA[C/T]ACCCACTAAACAGTA	5253
rs74614156	snp	C/T	0.077417	0.180873	intron-variant	PHF2	GRCh38.p7	9:93661325	AGGGGTGTAGTGGGA[C/T]GCTTTTGTGTTCTCT	5253
rs74647683	snp	A/G	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672828	TGGGTGTAGGTGTAG[A/G]AACAGGTGTAGATGC	5253
rs74749889	snp	A/G	0.000399281	0.0141238	intron-variant	PHF2	GRCh38.p7	9:93638416	AGTTTTAGCACATAC[A/G]GTTTGTTCTTTGATA	5253
rs74757513	snp	A/C	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93611884	AAAATATTCAATAAT[A/C]AAAAATTTGTCTCCA	5253
rs74780057	snp	A/T	0.0115144	0.0749975	intron-variant	PHF2	GRCh38.p7	9:93596327	GCCCCTGCATTTTTC[A/T]TTTAGCCCAAATTCA	5253
rs74797320	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93651534	ATGTTGGCCAAGCAG[A/G]TAAGGTCAGGCCTGA	5253
rs74824309	snp	A/T			intron-variant	PHF2	GRCh38.p7	9:93625115	CCACACCCACTAAAC[A/T]GTAACTCCTCATTCC	5253
rs74837131	snp	A/G	0.0648419	0.167978	intron-variant	PHF2	GRCh38.p7	9:93643273	TTGGGGTTCCCAACC[A/G]ATGGGTTTAGTGCAA	5253
rs74842678	snp	C/G	0.0785177	0.181917	intron-variant	PHF2	GRCh38.p7	9:93658926	GGTCTGGCCCAGCCT[C/G]GAGCACCCTCTGGGA	5253
rs74843792	snp	A/G	0.0733688	0.176922	intron-variant	PHF2	GRCh38.p7	9:93637711	GTGATGGTCATTTGC[A/G]TTGTTTCCACTTTTT	5253
rs74858391	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93599253	TTATTTTTACCGTCA[G/T]CGTCTTCATCTTCAA	5253
rs74912627	snp	C/G	0.0640965	0.167152	intron-variant	PHF2	GRCh38.p7	9:93597767	CCTTTTCATGTGCCC[C/G]TTACATTTGTGGGTT	5253
rs74921118	snp	C/G	0.0755793	0.179102	intron-variant	PHF2	GRCh38.p7	9:93675241	TGGGAGCCCAGATGT[C/G]CTTCTACACAGCCCC	5253
rs74928553	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93613162	AGGTGGCTCTGCTCT[A/G]TATGTGATTCCCATC	5253
rs74956334	snp	C/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618901	TGTTTGTGTGTGTGT[C/G]TATGTGCGTCTGCAT	5253
rs75018698	snp	A/G	0.0792508	0.182605	intron-variant	PHF2	GRCh38.p7	9:93647025	GTCTCGCCTGTGCTC[A/G]GCTTTACCGCAGGTT	5253
rs75067094	snp	A/C			intron-variant	PHF2	GRCh38.p7	9:93621509	GGAAGGAGGAAGCCC[A/C]CAAGGGGCCCCTCCT	5253
rs75143474	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93622729	AGTGAATCCTTCAGG[-/T]GGGCTCCTGTCCAAA	5253
rs75191194	snp	A/C	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93647889	ATGAGATTTCATCTC[A/C]AAAAAAAAAAATTCT	5253
rs75221812	snp	A/G	0.0376037	0.131863	intron-variant	PHF2	GRCh38.p7	9:93674596	TCTCAAGCTCCATGA[A/G]CAGATGTACGGAGGG	5253
rs75222852	snp	A/T	0.0356815	0.128715	intron-variant	PHF2	GRCh38.p7	9:93642410	TTTGATTTCCTTCTT[A/T]TAGAATTATATCTTT	5253
rs75271573	snp	A/G	0.0209421	0.100162	intron-variant	PHF2	GRCh38.p7	9:93659768	CTTGCCTTTGTGAGG[A/G]CTCAGGGTCCTAGGT	5253
rs75271749	snp	G/T	0.0130921	0.0798413	intron-variant	PHF2	GRCh38.p7	9:93674318	CCCACCAGCCACAGG[G/T]CATGCCCTACAGTGT	5253
rs75301893	snp	A/C	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623900	CTAGGGCCCAAGACC[A/C]TGGTGGCCTTGCAGG	5253
rs75508131	snp	A/G	0.0376037	0.131863	intron-variant	PHF2	GRCh38.p7	9:93577712	GGAAGATGGGGAGGG[A/G]GGAAGGAGGTAACGC	5253
rs75519210	snp	C/T	0.0759472	0.179459	intron-variant	PHF2	GRCh38.p7	9:93661448	GGATGGATGAATGGA[C/T]GAACAGACGGATGGA	5253
rs75520436	snp	G/T	0.0345262	0.126772	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666298	ACTGAGCCTCCTGCC[G/T]GGGGAGGTTATTGGG	5253
rs75555279	snp	A/T	0.0689305	0.172377	intron-variant	PHF2	GRCh38.p7	9:93656675	GGTCAGGGCTGACTG[A/T]CTGGGTGTGAGTGCC	5253
rs75558730	snp	C/T	0.0217236	0.101931	intron-variant	PHF2	GRCh38.p7	9:93637882	CCAAAGCAGGTTCCC[C/T]GTTTTACCTTCCCAC	5253
rs75625893	snp	A/G	0.234692	0.249531	intron-variant	PHF2	GRCh38.p7	9:93605006	CGTGATTTATTTTTA[A/G]TAGACTTAAGTTTTT	5253
rs75653373	snp	A/C	0.5	0	synonymous-codon	PHF2	GRCh38.p7	9:93676722	GCCAGCCTCTACCAC[A/C]CCGGCCTCCACCACC	5253
rs75655550	snp	A/G	0.0310518	0.120672	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93667557	ACATGTACTACAGAC[A/G]GGTAACTCAGGGGGC	5253
rs75661935	snp	A/G	0.0217236	0.101931	intron-variant	PHF2	GRCh38.p7	9:93648417	CAGTGATGCAGACAA[A/G]GCCAGTGGCCCCGGC	5253
rs75678521	snp	C/T	0.234401	0.249513	intron-variant	PHF2	GRCh38.p7	9:93600744	GCTCGGCCCAAGCAG[C/T]CACACCCAGACCCTG	5253
rs75729879	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93617146	CCAGGGCCAGGTGTC[A/G]GTCATTCCTGGCTGG	5253
rs75742615	snp	A/T			intron-variant	PHF2	GRCh38.p7	9:93610072	ATGCCTAGGTGTAGA[A/T]TTTTTTTTGCGGGGA	5253
rs75746788	snp	A/G	0.0217236	0.101931	intron-variant	PHF2	GRCh38.p7	9:93662776	TGGGTGAATGGATGC[A/G]TGGATGGGTAGATGG	5253
rs75747686	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93624052	AGGGCAGTACTATCC[C/T]TAGTGAATGAATAAG	5253
rs75748099	snp	A/G	0.0209421	0.100162	intron-variant	PHF2	GRCh38.p7	9:93645577	GTCCACACCTGTCCC[A/G]GTGCAGGAGGCCTCG	5253
rs75762876	in-del	-/AAA/AAT			intron-variant	PHF2	GRCh38.p7	9:93608336	CATAATAATAATAAT[-/AAA/AAT]TATTATTTTTGTACA	5253
rs75781370	snp	C/T	0.0861826	0.188849	intron-variant	PHF2	GRCh38.p7	9:93655084	TGTGCCCCTAGATGA[C/T]GTTAGAACAAATCCC	5253
rs75805906	snp	A/G	0.029116	0.117091	intron-variant	PHF2	GRCh38.p7	9:93580149	CAAGATTCCTCCTCC[A/G]GCCCCATCTTGACCG	5253
rs75817819	snp	G/T	0.0314385	0.121371	intron-variant	PHF2	GRCh38.p7	9:93659760	TGGGCAAGCTTGCCT[G/T]TGTGAGGGCTCAGGG	5253
rs75843233	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623786	CTAAGATAGAGTGAA[C/T]TTTATATTTTCAAAA	5253
rs75881059	snp	A/T			intron-variant	PHF2	GRCh38.p7	9:93614488	GAAGGCATCATGGCT[A/T]GGGAGGAAGAAACTT	5253
rs75894380	snp	A/G	0.0267878	0.112589	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93671025	CAGGTCTATGTTCAG[A/G]TGGGTGCAGGTGTGG	5253
rs75947939	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93652307	TTTTTTTTTTTTTTT[G/T]TTTTGGAGATGGAGT	5253
rs75952566	snp	C/T	0.0562307	0.157967	intron-variant	PHF2	GRCh38.p7	9:93646076	TATGAATTGCATTAC[C/T]GTGGGTGCTACATGA	5253
rs75952968	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623930	GGTTAGTCTGATACA[C/T]TGGGCACTAGCAGTA	5253
rs75984325	snp	C/G	0.0267878	0.112589	intron-variant	PHF2	GRCh38.p7	9:93581245	AGGCAGAGCCATGTT[C/G]AGGGGCTACCTGGGA	5253
rs76025942	snp	A/G	0.104149	0.203046	intron-variant	PHF2	GRCh38.p7	9:93605618	TACTTTACTGTCTCC[A/G]TAGCTTTGCCTTTTG	5253
rs76045678	snp	A/G	0.0770498	0.180522	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669011	AGTGTTTATTGCTGG[A/G]GGAAAAGGAAAGGAT	5253
rs76085004	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618902	GTTTGTGTGTGTGTG[C/T]ATGTGCGTCTGCATG	5253
rs76133471	snp	G/T	0.0433465	0.140692	intron-variant	PHF2	GRCh38.p7	9:93619781	GAAGAAACTCAGGGG[G/T]TGCTGCTCTTAGCCA	5253
rs76158659	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623940	ATACACTGGGCACTA[A/G]CAGTAACAGCTCACT	5253
rs76202832	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93621394	TCCTGCACAAAGCAG[C/T]AAATGACTGACCAAG	5253
rs76206046	snp	C/T	0.0298908	0.118541	intron-variant	PHF2	GRCh38.p7	9:93643464	TTTCTTCTTCCTCAC[C/T]GTCTAGTCCCCCCTG	5253
rs76244171	snp	A/G	0.0759472	0.179459	intron-variant, utr-variant-3-prime	PHF2, LOC107987098	GRCh38.p7	9:93673473	CGCCCTCTGCCTGCC[A/G]CCTGGGCCAGGAGTT	5253
rs76256243	snp	G/T	0.0128227	0.0790376	intron-variant	PHF2	GRCh38.p7	9:93658132	CCCACCTCACCCAGT[G/T]TCTCCTTCCCAGGCT	5253
rs76258509	snp	C/T	0.0314385	0.121371	intron-variant	PHF2	GRCh38.p7	9:93583730	AATGTCTACTCAAGG[C/T]CTTTGCCCACTTTTA	5253
rs76290025	snp	A/T	0.142531	0.232644	intron-variant	PHF2	GRCh38.p7	9:93608100	GGTCTTGTCTTACCT[A/T]ATTGTATTAGCTAGA	5253
rs76290383	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93624026	TTGCATGTGTAAATG[C/T]CCCAAGGGCAAGGGC	5253
rs76356305	snp	A/G	0.0379877	0.132479	intron-variant	PHF2	GRCh38.p7	9:93603363	GCTGGCATTTCCGGC[A/G]ACAGAGTTTAGGGCA	5253
rs76380815	snp	A/C			intron-variant	PHF2	GRCh38.p7	9:93622840	CCCTGCTAACTGAGC[A/C]CCGAGTCTGTCTGTC	5253
rs76433012	snp	A/G	0.0640965	0.167152	intron-variant	PHF2	GRCh38.p7	9:93613182	TGATTCCCATCAGTC[A/G]TGTTTGGGGTTTTCT	5253
rs76485984	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93611515	TTGGATTAAAAATAT[C/T]CCTTTTATTTTTTAA	5253
rs76488437	snp	A/C	0.234982	0.249549	intron-variant	PHF2	GRCh38.p7	9:93605514	CTATCCATCCCTCCC[A/C]GTACCCCCAAACCTC	5253
rs76499753	snp	A/C	0.0759472	0.179459	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93670155	TGATGCTGATGCAAG[A/C]GTCCTGAAGGGGCAG	5253
rs76557088	snp	C/T	0.0283406	0.115616	intron-variant	PHF2	GRCh38.p7	9:93621557	TGTGCCAGGGCAGAG[C/T]GTCCTAAAGTGGACA	5253
rs76581097	snp	G/T	0	0	intron-variant	PHF2	GRCh38.p7	9:93602268	TTTTTTTTTTTTTTT[G/T]TTGAGATGGAATCTT	5253
rs76587011	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623853	TGTTCCCAGAACTCA[A/G]GACTGTGGTGGCTGT	5253
rs76636570	in-del	-/T	0.290977	0.246619	intron-variant	PHF2	GRCh38.p7	9:93592408	AAATTATCTGCATCC[-/T]TTTGCCTAGTGATTT	5253
rs76656247	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93624053	GGGCAGTACTATCCT[C/T]AGTGAATGAATAAGG	5253
rs76672364	snp	A/G	0.0770498	0.180522	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668260	TCCTGCTTGGCACTA[A/G]GTGGTTCCTGTCCAT	5253
rs76717512	snp	A/G	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672794	GGTATAGGAGTAGGT[A/G]CAGGTGTAGATGCAT	5253
rs76725109	snp	C/T	0.0785177	0.181917	intron-variant	PHF2	GRCh38.p7	9:93639802	GAAGTGGAAGTCCTG[C/T]TCTCCCAAGAAGAAA	5253
rs76746406	snp	A/G	0.0614824	0.164198	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666256	ACAGTGGTCATCTCT[A/G]CCTGGGCGTGCGAGG	5253
rs76751209	snp	C/T	0.00716266	0.059414	intron-variant	PHF2	GRCh38.p7	9:93652733	GACGTGGCCAGGGGT[C/T]GTGGGCACCCTGTTG	5253
rs76780171	snp	A/G	0.0337553	0.125452	intron-variant	PHF2	GRCh38.p7	9:93677446	GCTGAGCTCGGAGCT[A/G]GGGCTTCATAGGCCC	5253
rs76781920	snp	C/T	0.00517822	0.0506191	intron-variant, utr-variant-3-prime	PHF2, LOC107987098	GRCh38.p7	9:93673235	GGAAGGTCACTGAGT[C/T]GGCTTGCTGGCTTTA	5253
rs76810945	in-del	-/G	0.0700422	0.173537	upstream-variant-2KB	PHF2	GRCh38.p7	9:93575053	AGAGGTGTGGGAGCT[-/G]GGGGTCTCCTGCTCT	5253
rs76823381	snp	A/G	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672830	GGTGTAGGTGTAGGA[A/G]CAGGTGTAGATGCAG	5253
rs76832193	snp	A/C	0.5	0	missense	PHF2	GRCh38.p7	9:93660330	CTGGAGAAAGTGTCC[A/C]AAAAAAAGACTCCCA	5253
rs76834016	snp	C/G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623975	AACGAGTGTTCACTC[C/G/T]GGGCCAGGCCCACCC	5253
rs76863038	snp	C/T	0.0759472	0.179459	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93666143	TGAGTGACTCCAGGG[C/T]GGTCTCTGGGGGTGT	5253
rs76868268	snp	A/G	0.0569829	0.158885	intron-variant	PHF2	GRCh38.p7	9:93598966	GGTATGTCCGTGTGC[A/G]CCCTTGGAAGCAGCA	5253
rs76883066	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93616720	GAGTGCAATGGCTCA[A/G]TCTCGGCTCACCGCA	5253
rs76886547	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93621146	TAGCAGGGGATCTGG[C/T]CTGGATCCCTGTGGA	5253
rs76903385	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93607464	TTTTTTTTTTTTTTG[G/T]TAGGGAGAGGGTTTC	5253
rs76904320	snp	A/T	0.0637235	0.166737	intron-variant	PHF2	GRCh38.p7	9:93597665	GGAGGAGCCTGGTGT[A/T]GTCCTGAGGTGAGGG	5253
rs76962843	snp	A/G/T			intron-variant	PHF2	GRCh38.p7	9:93631401	GCTCTTCCTGAACTT[A/G/T]CAGGCTGATAGTTTG	5253
rs77002154	snp	A/G	0.0213758	0.101148	intron-variant	PHF2	GRCh38.p7	9:93608009	TGAGAGAGAGAGAGA[A/G]AAGGAAAGGAGGAAG	5253
rs77017842	snp	A/G	0.0209421	0.100162	intron-variant	PHF2	GRCh38.p7	9:93655008	GCTAGCTGCTAATTA[A/G]GACAATAGTAGGGGA	5253
rs77030578	snp	A/C			intron-variant	PHF2	GRCh38.p7	9:93616732	TCAATCTCGGCTCAC[A/C]GCAACCTCCGCCTCC	5253
rs77133953	snp	G/T	0.0777841	0.181223	intron-variant	PHF2	GRCh38.p7	9:93635287	ATTGTCACTGGGTGG[G/T]CATTAGCTCCCTTTG	5253
rs77286250	snp	C/T	0.0737376	0.17729	intron-variant	PHF2	GRCh38.p7	9:93674209	TTCCTCGACAGGCCC[C/T]GGAGGTTGAAGGACC	5253
rs77292045	snp	C/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623924	TTGCAGGGTTAGTCT[C/G]ATACACTGGGCACTA	5253
rs77302343	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93655289	TGGTTTTTTTTTTTT[C/T]TCATTTTAAATAAGT	5253
rs77331348	snp	A/G	0.0325976	0.123435	intron-variant	PHF2	GRCh38.p7	9:93598960	GTGGCTGGTATGTCC[A/G]TGTGCGCCCTTGGAA	5253
rs77337973	snp	C/T	0.00993419	0.0697739	intron-variant	PHF2	GRCh38.p7	9:93650386	CATACTCCTAACACC[C/T]GCATCCCTGGCACAG	5253
rs77393931	snp	C/T	0.121369	0.214369	intron-variant	PHF2	GRCh38.p7	9:93583830	TTTTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTT	5253
rs77398150	snp	C/T	0.0111196	0.0737302	intron-variant	PHF2	GRCh38.p7	9:93584642	CTGCTTTGATTACTG[C/T]AAAGTTGTAGTAAGT	5253
rs77405940	snp	A/T	0.00501934	0.0498445	intron-variant	PHF2	GRCh38.p7	9:93636532	CTTTCCCAGGTGGGC[A/T]GGCCTTCCTGTATGC	5253
rs77448876	snp	C/G	0.0349115	0.127424	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671061	GGTGCAGGTGTAGAT[C/G]CAGGTGGGGGTGCAG	5253
rs77486680	in-del	-/T			intron-variant	PHF2	GRCh38.p7	9:93612274	AGGACATGTAACAGG[-/T]GTCTGTGTCTAAAAT	5253
rs77586221	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93617109	GGAGGGTGGCATGGT[C/T]GGAGGGTGTCTGAGC	5253
rs77601841	snp	C/T	0.0150606	0.0854603	intron-variant	PHF2	GRCh38.p7	9:93654311	GTTGCAGGCGGGAGT[C/T]GTGGACCTGGGCAGG	5253
rs77606993	snp	A/C	0.0486741	0.148216	intron-variant	PHF2	GRCh38.p7	9:93577821	TCCCACCAAGAAGTA[A/C]ATGGAGGAGGAGGAA	5253
rs77620025	snp	A/G	0.0558544	0.157504	intron-variant	PHF2	GRCh38.p7	9:93619730	GTTGCGGCCCCTGAA[A/G]TTTGCACTTCGGCCA	5253
rs77626301	snp	A/G	0.00517822	0.0506191	intron-variant	PHF2	GRCh38.p7	9:93601033	ACTGAATAGCCTTCC[A/G]TTGTGCTATGGTGGT	5253
rs77671970	snp	C/G			intron-variant	PHF2	GRCh38.p7	9:93625145	CTCTCTCCTCCCACC[C/G]TCTGGCACCACTAGT	5253
rs77678872	snp	A/G	0.0737376	0.17729	intron-variant	PHF2	GRCh38.p7	9:93606950	CACCATTTGTTGATC[A/G]GACTGTTTTGTCTCC	5253
rs77685886	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93665885	TTGGGAGGGGGTGTT[G/T]GGGGAGGGGTGTGGG	5253
rs77688649	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93616666	ATTTTTTTTTTTTTT[C/T]TGAAACAGAGTTTCG	5253
rs77710603	snp	A/G	0.0770498	0.180522	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669565	GAAACCCAAAATGCA[A/G]CGCAGTCCAGTATGT	5253
rs77748276	snp	C/G	0.0107246	0.0724382	intron-variant	PHF2	GRCh38.p7	9:93630934	CACATCTCTGCTGAC[C/G]TGAGCCCTGGACAAG	5253
rs77768484	snp	A/G	0.0948562	0.196037	intron-variant	PHF2	GRCh38.p7	9:93622011	CACCTGGGGCATTTG[A/G]GGGCCTTTCCATGCA	5253
rs77774636	snp	A/G	0.0614824	0.164198	intron-variant	PHF2	GRCh38.p7	9:93628371	GGGATTTTCTTTTTG[A/G]GGGAGGTTTTTTGAT	5253
rs77774853	snp	C/G/T	0.000399281	0.0141238	intron-variant	PHF2	GRCh38.p7	9:93624128	CTCAATTTCCCTATT[C/G/T]TGGTAAATAAGGCTA	5253
rs77823023	snp	A/G	0.0322114	0.122752	intron-variant	PHF2	GRCh38.p7	9:93581940	AATCTCACTTTTGAA[A/G]TTCAGGGTGTGGGTA	5253
rs77836180	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93620735	CTTCAGATTCTCAGT[A/G]TCTTATGCTCCTGGC	5253
rs77858114	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93614493	CATCATGGCTTGGGA[A/G]GAAGAAACTTTGGGT	5253
rs77895198	snp	A/G	0.00597247	0.0543191	intron-variant	PHF2	GRCh38.p7	9:93636253	CCTCCCTATGTGCAT[A/G]GCAGGGTGGGGGTGT	5253
rs77897038	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93613024	GCTGGTGCCAGGCCC[C/T]TAGGCTTCCTGGTCA	5253
rs77902674	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93612251	ATGATCCACGTATCT[A/G]TGGGGAGAGGACATG	5253
rs77915501	snp	A/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93608334	TCTCATAATAATAAT[A/T]ATTATTATTTTTGTA	5253
rs77922475	snp	A/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623944	ACTGGGCACTAGCAG[A/T]AACAGCTCACTGTCT	5253
rs77923071	snp	A/T	0.5	0	intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93672829	GGGTGTAGGTGTAGG[A/T]ACAGGTGTAGATGCA	5253
rs77939363	snp	C/T	0.0325976	0.123435	intron-variant	PHF2	GRCh38.p7	9:93590384	AAGGGCGCCCCACTT[C/T]GATGGGCTGGGAACA	5253
rs77948146	snp	A/G	0.0707826	0.174302	intron-variant	PHF2	GRCh38.p7	9:93675340	GGTCACCTTTGTACC[A/G]GAGGCACCCACTTGA	5253
rs77978457	snp	C/T	0.0652144	0.168387	intron-variant	PHF2	GRCh38.p7	9:93583149	ATTTACTATTTCATA[C/T]GAATAGAATCATACA	5253
rs78152024	snp	A/G	0.0182019	0.0936463	intron-variant	PHF2	GRCh38.p7	9:93664872	TAAGGCAGCGGGCTC[A/G]CCGCCCCTTCACTTA	5253
rs78174934	snp	A/G	0.0948562	0.196037	intron-variant	PHF2	GRCh38.p7	9:93627397	TTTTTCTGTGTATGG[A/G]TTCCTTTAGAGTTTT	5253
rs78206870	snp	C/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623878	GGCTGTGGAACAGAA[C/G]ACTCGTCTAGGGCCC	5253
rs78226967	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93652315	TTTTTTTTTTTTGGA[G/T]ATGGAGTCTCACTCT	5253
rs78254907	snp	G/T			missense	PHF2	GRCh38.p7	9:93659549	TAGCTGTGAAGGTTT[G/T]AAGTGCTCCGGGAGC	5253
rs78266236	snp	C/T	0.0325976	0.123435	intron-variant	PHF2	GRCh38.p7	9:93662754	GGTGAATGGGTACAT[C/T]GATGGGTGGGTGAAT	5253
rs78335081	snp	A/G	0.00119737	0.0244387	intron-variant	PHF2	GRCh38.p7	9:93590996	AGTGTGGACATCCCA[A/G]CAGCTCCGGGGCCAT	5253
rs78337831	snp	C/T	0.00431245	0.0462345	intron-variant, downstream-variant-500B	PHF2, LOC107987098	GRCh38.p7	9:93673879	TGAGTGTCACTCCTG[C/T]GTGGGGCAGGGCCCA	5253
rs78361903	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93613892	ATTGTCAGACCAGAA[A/G]TCTCTATGGGTTGTC	5253
rs78381544	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93623049	AGATGCTGCAGTGAG[A/G]GCACAGCCTGGAGCA	5253
rs78382492	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93613185	TTCCCATCAGTCGTG[C/T]TTGGGGTTTTCTTTG	5253
rs78407785	snp	A/C	0.00821679	0.0635679	intron-variant	PHF2	GRCh38.p7	9:93662892	CCTCTGGGTCACAGC[A/C]GCCCTTTTTTCTAGG	5253
rs78409257	snp	A/C	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93624009	TCTTTGCCTGGCTTC[A/C]TTTGCATGTGTAAAT	5253
rs78487718	snp	C/T	0.00119737	0.0244387	intron-variant	PHF2	GRCh38.p7	9:93598249	GCAGCACACTGTGGA[C/T]GGGTTATTTTGACAA	5253
rs78521668	snp	C/T	0.0279526	0.114869	intron-variant	PHF2	GRCh38.p7	9:93674420	CCCTTTTCATAGCAA[C/T]GGAAGGAGTTGTGAG	5253
rs78522617	snp	A/G	0.0341408	0.126114	intron-variant	PHF2	GRCh38.p7	9:93655143	CACTATTTCTGAAGG[A/G]CTTCCTTTCCTTCTA	5253
rs78544667	snp	C/T	0.084364	0.187256	intron-variant	PHF2	GRCh38.p7	9:93636779	TGGTGACCTTTCTCC[C/T]GCTGGGTGGAAGGGA	5253
rs78547192	snp	C/G	0.103794	0.20279	intron-variant	PHF2	GRCh38.p7	9:93597221	GGTGTGAGCCATCGC[C/G]CCTGGCCTCTGCCAA	5253
rs78619366	snp	G/T	0.103082	0.202275	intron-variant	PHF2	GRCh38.p7	9:93590541	TTGTTTGACTCTTGT[G/T]GTGAGGCCAAGCCTC	5253
rs78644344	snp	C/T	0.107341	0.205301	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93665491	TCCTGTCTGCAGAGG[C/T]TTGGGCCCTCTACCC	5253
rs78663083	snp	G/T	0	0	intron-variant	PHF2	GRCh38.p7	9:93605235	TTTTATACATTTTTT[G/T]GAAACAGGGTCTTGC	5253
rs78679201	snp	A/G	0.0158469	0.0875917	intron-variant	PHF2	GRCh38.p7	9:93585329	CTCCTTTCCCTGACC[A/G]CCATCCTCCCCAGGG	5253
rs78737444	snp	C/G	0.0327778	0.123752	intron-variant	PHF2	GRCh38.p7	9:93587502	TGATGGAGGAGCCCC[C/G]GGTGAGGGATGATGG	5253
rs78738062	in-del	-/CT	0.234692	0.249531	intron-variant	PHF2	GRCh38.p7	9:93616394	TCCCAAGTTAGTCCC[-/CT]GACTAGAAGGGTAAG	5253
rs78763959	snp	A/G	0.00914312	0.0669923	intron-variant	PHF2	GRCh38.p7	9:93657208	AGTTTGCATTTATGC[A/G]TGATTTCCTTTCTCG	5253
rs78792144	snp	C/T	0.103438	0.202533	intron-variant	PHF2	GRCh38.p7	9:93583725	GGACAAATGTCTACT[C/T]AAGGCCTTTGCCCAC	5253
rs78814851	snp	A/G	0.104149	0.203046	intron-variant	PHF2	GRCh38.p7	9:93590652	ATCTCCACATACCCC[A/G]GCCAGTGTTCCTGAA	5253
rs78816659	snp	C/T	0.113334	0.209338	upstream-variant-2KB	PHF2	GRCh38.p7	9:93575141	GCTTTGGGCACTGCC[C/T]TGAGTCTGTATCCAC	5253
rs78925720	snp	G/T	0.0154538	0.0865337	intron-variant	PHF2	GRCh38.p7	9:93602843	GTTGCCCCTCAAAGG[G/T]TCACTTAGGTGTGGC	5253
rs78954488	snp	C/T	0.0107246	0.0724382	intron-variant	PHF2	GRCh38.p7	9:93663965	CCCTGCCTCCCACCA[C/T]GCTCCACCTGTAGTG	5253
rs79012365	snp	C/T	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93672825	GTATGGGTGTAGGTG[C/T]AGGAACAGGTGTAGA	5253
rs79015032	snp	C/T	0.0205511	0.0992634	intron-variant	PHF2	GRCh38.p7	9:93664128	AGCTGGTGCTGAGGA[C/T]GTGCATGGGGGACAG	5253
rs79020256	snp	A/G	0.00834362	0.0640484	intron-variant	PHF2	GRCh38.p7	9:93674897	TGCCCTGCACTCAGC[A/G]GGCCACGCCTTCCCT	5253
rs79049472	snp	G/T	0.0984431	0.198823	intron-variant	PHF2	GRCh38.p7	9:93647116	TCAGGCAGCCTTGTG[G/T]ACCCCAGCTGTAATG	5253
rs79054517	snp	A/G	0.0410537	0.137264	intron-variant	PHF2	GRCh38.p7	9:93676541	GGAGCTCCCTGCTCT[A/G]TTGGCCCAAGTGGGC	5253
rs79056932	snp	A/G	0.103794	0.20279	intron-variant	PHF2	GRCh38.p7	9:93585431	AGAGTAGGGACAGCA[A/G]GCACAGTTATGGAGC	5253
rs79124552	snp	A/C			intron-variant	PHF2	GRCh38.p7	9:93675947	ATTAGAGAGTGCCCT[A/C]TTCCTCCAGGCCCTA	5253
rs79215583	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93623941	TACACTGGGCACTAG[C/T]AGTAACAGCTCACTG	5253
rs79219706	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618899	TATGTTTGTGTGTGT[G/T]TGTATGTGCGTCTGC	5253
rs79247476	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93625035	GTGGTACTTAGTAAA[G/T]TCACAATGCTATGCA	5253
rs79286054	snp	A/G	0.0115144	0.0749975	intron-variant	PHF2	GRCh38.p7	9:93590072	CTGCTGGATATATTC[A/G]AATAAGTAAAGTTGC	5253
rs79299534	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93624010	CTTTGCCTGGCTTCC[G/T]TTGCATGTGTAAATG	5253
rs79329731	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93622842	CTGCTAACTGAGCCC[C/T]GAGTCTGTCTGTCTG	5253
rs79332603	snp	A/G	0.0376037	0.131863	intron-variant	PHF2	GRCh38.p7	9:93577782	GATGGCCATGACCTG[A/G]CCCCATGCCTAGGGC	5253
rs79364474	snp	A/G	0.0130921	0.0798413	intron-variant	PHF2	GRCh38.p7	9:93630612	AAGGGCTGAGGCTTC[A/G]TTTTCTTCTTGGCCC	5253
rs79380127	snp	C/G	0.0322114	0.122752	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678159	GATGTTTATGTCCCC[C/G]CTTCTCTTCCTGAGT	5253
rs79391190	snp	C/G	0.0770498	0.180522	intron-variant	PHF2	GRCh38.p7	9:93637992	GCGAGTGGGTATGAA[C/G]TGGTATCTTATTTTT	5253
rs79403358	snp	A/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93647900	TCTCAAAAAAAAAAA[A/T]TTCTTTTTATATACA	5253
rs79407619	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93677371	CTACCTGCCAGGGCC[C/T]CTTGAGGACACGGCC	5253
rs79432875	snp	C/T	0.000798403	0.0199641	intron-variant	PHF2	GRCh38.p7	9:93588320	GGGACCATGGGACTG[C/T]GGGATAGAGGGGAGC	5253
rs79443824	snp	C/T	0.0718919	0.175435	intron-variant	PHF2	GRCh38.p7	9:93647515	CAGTAAGCCCTCATG[C/T]ACTCAGCACCAGAAA	5253
rs79526768	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93620676	GAAGTCATCTGCTAA[C/T]ATGGCCTTGGGATGC	5253
rs79530803	snp	C/G/T			intron-variant	PHF2	GRCh38.p7	9:93622196	TAGGACTTCCTTACA[C/G/T]TCACAGGCACTGCTG	5253
rs79554354	snp	G/T	0.0644693	0.167566	intron-variant	PHF2	GRCh38.p7	9:93583053	GGTATCCAATAAGTA[G/T]TCACTGCCCTTTCTT	5253
rs79565493	snp	C/G	0.0770498	0.180522	intron-variant	PHF2	GRCh38.p7	9:93634820	GTCTGTTAGGAGCAC[C/G]AAGCCAGCCTGTGAG	5253
rs79570451	snp	A/C			intron-variant	PHF2	GRCh38.p7	9:93654645	GCTTACTGCCCTGTC[A/C]CTTGGACCGTGTCCC	5253
rs79610414	snp	C/G			intron-variant	PHF2	GRCh38.p7	9:93621074	AAGTGGCCACTGTCG[C/G]GGTTGGTGGCACAGG	5253
rs79630334	snp	A/T	0.00119737	0.0244387	intron-variant	PHF2	GRCh38.p7	9:93631769	CAGGAGGTGCTTTCC[A/T]GGGGGGTAGGACCCT	5253
rs79690230	snp	C/T	0.000399281	0.0141238	intron-variant	PHF2	GRCh38.p7	9:93623789	AGATAGAGTGAACTT[C/T]ATATTTTCAAAAACA	5253
rs79708182	snp	A/G	0.00645734	0.0564533	synonymous-codon, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93667106	CTCGGACGAGGGTTC[A/G]CTGCACATCGACACA	5253
rs79717229	snp	C/T	0.00597247	0.0543191	intron-variant	PHF2	GRCh38.p7	9:93590302	AGAGTTGTAGAGTTG[C/T]GTCAGTAGCCCTGGT	5253
rs79721265	snp	A/G	0.0205511	0.0992634	intron-variant	PHF2	GRCh38.p7	9:93582776	TATCAAAGCTTTCCA[A/G]AGGAGGCGTGTCTTG	5253
rs79730252	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93613922	CAGCTCCTGGGCTGG[C/T]CCCTCTCCTCCTGGC	5253
rs79734557	snp	A/C/G	0.0298908	0.118541	intron-variant	PHF2	GRCh38.p7	9:93644563	TGCACTCCTCCCCTC[A/C/G]GCCCTGTCTTGCAGG	5253
rs79773322	snp	C/T	0.0263992	0.111815	intron-variant, utr-variant-3-prime	PHF2, LOC107987098	GRCh38.p7	9:93673122	ACATGGGAAGGTTCC[C/T]TACAAAGTGGGGTAA	5253
rs79775104	snp	A/G	0.00413917	0.045304	intron-variant	PHF2	GRCh38.p7	9:93653375	CTCAAGGTGAGCCAC[A/G]CCCCTCGGGGCACCT	5253
rs79849140	snp	A/G	0.0441095	0.141807	intron-variant	PHF2	GRCh38.p7	9:93598160	CATCTGCCTGGTGAC[A/G]CCCCAGGGATGGGGC	5253
rs79932852	snp	C/G	0.0912534	0.193131	intron-variant	PHF2	GRCh38.p7	9:93619082	CCTCGCTTGCCTGTG[C/G]AGAGGTGGATCACCC	5253
rs79940477	snp	C/T	0.0414363	0.137845	intron-variant	PHF2	GRCh38.p7	9:93661235	ACCCCTGAAGCACCA[C/T]TGAGTGTGAGTTTCT	5253
rs79962091	snp	C/T	0.5	0	missense	PHF2	GRCh38.p7	9:93660340	TGTCCAAAAAAAAGA[C/T]TCCCAAAACTGTGAA	5253
rs79986053	snp	A/T			intron-variant	PHF2	GRCh38.p7	9:93611995	CCTGTGTGTCTTTCC[A/T]GAACATTCTGATTAC	5253
rs79987346	snp	A/G	0.0948562	0.196037	intron-variant	PHF2	GRCh38.p7	9:93622467	GATGACCCAGCAGCT[A/G]CAGCGTCATCACAGT	5253
rs80032681	snp	A/G	0.0655868	0.168795	intron-variant	PHF2	GRCh38.p7	9:93637656	ATGATATTTCATCGT[A/G]TAGATATCCACATAG	5253
rs80062429	snp	C/T	0.234692	0.249531	intron-variant	PHF2	GRCh38.p7	9:93608830	AATTTTATTTATTTG[C/T]TTTTTAATCCACTCT	5253
rs80067224	snp	C/G/T	0.0376113	0.131917	intron-variant	PHF2	GRCh38.p7	9:93579250	TCCTGATCTTCGTAC[C/G/T]GCCTGTACTGTGATT	5253
rs80069215	snp	A/G	0.0329836	0.124112	intron-variant	PHF2	GRCh38.p7	9:93596236	ATTGGGACCCCCTGT[A/G]CCCACGAGTGGAGGG	5253
rs80109961	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93621167	TCCCTGTGGAGGGTC[C/T]ACTTCCTTCAGCCTT	5253
rs80167093	in-del	-/TTTT			intron-variant	PHF2	GRCh38.p7	9:93598510	ACCCCCGTCAGAAGT[-/TTTT]GGGTTGTGTCCATGA	5253
rs80173486	snp	C/T	0.0755793	0.179102	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93665949	GGGTGGCTGGCTCCC[C/T]GCAAGGCCTCCCGCT	5253
rs80198318	snp	C/G	0.078151	0.181571	intron-variant	PHF2	GRCh38.p7	9:93653904	ATCTGGGGGCGGGCA[C/G]GTGCACATGCTGATC	5253
rs80199733	snp	C/T	0.00517822	0.0506191	intron-variant	PHF2	GRCh38.p7	9:93653599	GATGGGATTCAGGCT[C/T]GTTAACAATTGGGTG	5253
rs80206098	snp	C/G			intron-variant	PHF2	GRCh38.p7	9:93616734	AATCTCGGCTCACCG[C/G]AACCTCCGCCTCCTG	5253
rs80220512	snp	A/C			intron-variant	PHF2	GRCh38.p7	9:93622796	GCCAAGTCTTGTCCC[A/C]AGAACAGGCATGTTC	5253
rs80228675	snp	A/G	0.0766824	0.180169	intron-variant	PHF2	GRCh38.p7	9:93637918	GGGTATGAGGGTCTC[A/G]ATTTCTTCACATCCT	5253
rs80253797	snp	C/T	0.0209421	0.100162	intron-variant	PHF2	GRCh38.p7	9:93658001	TTCCAAGAGGAACTG[C/T]TGGCAGTTGAGCTGG	5253
rs80270017	snp	C/G/T	0.444444	0.157135	intron-variant	PHF2	GRCh38.p7	9:93618897	CATATGTTTGTGTGT[C/G/T]TGTGTATGTGCGTCT	5253
rs80292643	snp	A/G	0.00517822	0.0506191	downstream-variant-500B	PHF2	GRCh38.p7	9:93679842	CTTTTGGACTCAAGG[A/G]TATGGCGTTTGGCTG	5253
rs80294194	snp	C/G	0.0770498	0.180522	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93671010	GTGCAGATGCAGCTG[C/G]AGGTCTATGTTCAGG	5253
rs80327122	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93622193	GACTAGGACTTCCTT[A/G]CATTCACAGGCACTG	5253
rs111066151	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93624684	ATGGTGATGATGATG[A/G]TGGTGGTGGCGATGG	5253
rs111162496	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93624492	CGGTGATGGTGATGG[C/T]GGTGATGGTGATGAC	5253
rs111207194	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93624627	GGTTGAGATGATGAT[G/T]ATAATGATGGTGTGG	5253
rs111207195	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93624645	AATGATGGTGTGGCA[A/G]TGTTGGTGATGGTGT	5253
rs111207196	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93624652	GTGTGGCAATGTTGG[C/T]GATGGTGTTGGTGGT	5253
rs111207197	snp	A/G	0.0607341	0.163335	intron-variant	PHF2	GRCh38.p7	9:93662271	TCGATGGATAAATGA[A/G]TGGATGGGTAGATGG	5253
rs111254863	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93612103	GCTCTTTGCTGAACA[A/G]TATACATCCTGGAAA	5253
rs111258002	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93622538	TGTGAGAGCTCGGCT[A/G]GCCATCACTGGCTTT	5253
rs111258945	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93628313	GAAGGATTGGTGTTA[C/T]TCTTCTTTAAATGTT	5253
rs111266558	snp	A/G	0.00438332	0.0466095	intron-variant	PHF2	GRCh38.p7	9:93597725	CCTTAGGCCTATGTG[A/G]CACTGCAGTCACCTT	5253
rs111276080	snp	C/T	0.00358779	0.0422022	intron-variant	PHF2	GRCh38.p7	9:93637262	TGACCCTTCTCTGGG[C/T]AAGGTGTTTTTTTCC	5253
rs111278642	snp	A/C/T	0.000399281	0.0141238	intron-variant	PHF2	GRCh38.p7	9:93649740	AGACATTCATGACAC[A/C/T]CTGACCCTCACATTC	5253
rs111368969	snp	C/T	0	0	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678798	AGAGTTCTTCATTAA[C/T]ATTTATACGAGTTTT	5253
rs111374021	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93616664	TAATTTTTTTTTTTT[C/T]TCTGAAACAGAGTTT	5253
rs111377441	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93675650	GGCTGTGGCCTACAG[C/T]TTGAGGGGGCTGGCC	5253
rs111494831	snp	C/G	0.0337553	0.125452	intron-variant	PHF2	GRCh38.p7	9:93580065	GTGTGGAGTAGAGGT[C/G]GGGGAAACAGGCCCT	5253
rs111500486	snp	C/G	0.0383715	0.133092	intron-variant	PHF2	GRCh38.p7	9:93629574	GGCTCTGAGCTGCCT[C/G]TGGTGTTTTCTGCCC	5253
rs111507009	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93614940	GATGGTGATGATGGC[A/G]ATGGTGATGATGATG	5253
rs111522793	snp	A/C	0.0948562	0.196037	intron-variant	PHF2	GRCh38.p7	9:93627518	TTTTTTGTCTAATTG[A/C]TCTGGCTAGAACTTC	5253
rs111582399	snp	G/T			intron-variant	PHF2, LOC107987098	GRCh38.p7	9:93672702	CAGGTGTAGATGCAG[G/T]TATGGGTATAGGAGT	5253
rs111597695	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93651483	GGTCGGGTCCATGGA[G/T]TGGGCTCTGCTTCAT	5253
rs111603823	snp	C/T	0.0205511	0.0992634	intron-variant	PHF2	GRCh38.p7	9:93663381	CACCCCGCAGTGGCC[C/T]GGGTGGCCACCAGAG	5253
rs111628453	snp	C/T	0.0337553	0.125452	intron-variant	PHF2	GRCh38.p7	9:93664314	GGCATGCTGGATGAG[C/T]CTCGGGGTGAGGCAA	5253
rs111639447	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93637136	TTGAAGGATAATTCC[A/G]CTGGACGCAGAATCC	5253
rs111667193	in-del	-/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618888	TGTGTTTGCATATGT[-/G]TTTGTGTGTGTGTGT	5253
rs111672114	snp	A/G	0.0383715	0.133092	intron-variant	PHF2	GRCh38.p7	9:93625848	GTAATTCTATGTTTA[A/G]TTTTCTGAGGAAACA	5253
rs111678484	snp	A/G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618827	GTGTCTGCATGTGTG[A/G/T]TGTGTGTGGTGTGTG	5253
rs111703361	snp	A/G	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671976	CAGGTGTAGATGCAG[A/G]TGTGGGTGTGGGAGT	5253
rs111740980	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93587647	GGGCTGGACTGGAGG[A/G]TGTCTAACCCTACCA	5253
rs111772181	snp	A/G	0.0399052	0.1355	upstream-variant-2KB	PHF2	GRCh38.p7	9:93575138	AGTGCTTTGGGCACT[A/G]CCCTGAGTCTGTATC	5253
rs111773987	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93587331	TTGAGGGATGATGGA[A/G]GAGCCCTGGGTGAGG	5253
rs111797908	snp	A/G	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671904	CAGGTGTAGATGCAG[A/G]TGTGGGTGTGGGAGT	5253
rs111802777	snp	G/T	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671652	CAGGTGTAGATGCAG[G/T]TGTGGGTGTGGATGT	5253
rs111821504	snp	C/T	0.000798403	0.0199641	intron-variant	PHF2	GRCh38.p7	9:93598841	AGGAATGCATTCCCC[C/T]AAGAAGCCCATCACC	5253
rs111832851	snp	A/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93627614	AGCTTTCAGTCTTTC[A/T]CCATTGTATACAATG	5253
rs111918506	snp	G/T	0.5	0	downstream-variant-500B	PHF2	GRCh38.p7	9:93679639	TCACCCTGGCAGTGA[G/T]GGTGGTGGGGAGGCT	5253
rs111937223	snp	C/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618844	GTGTGTGGTGTGTGT[C/G]TGTGCCTGTGTGTGG	5253
rs111945016	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	PHF2, LOC107987098	GRCh38.p7	9:93673988	GCTCAGCAAAACCCT[C/T]GGCCTCTGACTGCTG	5253
rs112017780	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	PHF2	GRCh38.p7	9:93679811	GAGGATGTCCTTGGG[A/C]AGCCTCTAGAACCTT	5253
rs112056687	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93656992	CCCCTTAGGCTCCCT[C/T]AGGGGCCTGGCAACT	5253
rs112077866	in-del	-/C	0.5	0	intron-variant, upstream-variant-2KB	PHF2, MIR548AU	GRCh38.p7	9:93594534	CACCCCAAGGGTCTA[-/C]TGCAAGTGGGGATCC	5253
rs112087911	snp	A/G			intron-variant	PHF2	GRCh38.p7	9:93577235	GCCGGGCATCCGGAG[A/G]GAGGCCGAGGCCCGG	5253
rs112101838	in-del	-/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93616651	ATGTTTCTCCTATAA[-/T]TTTTTTTTTTTTTTC	5253
rs112132708	snp	C/T	0.029116	0.117091	upstream-variant-2KB	PHF2	GRCh38.p7	9:93575257	GTGGAGCAAACGGCC[C/T]CTTGGCAGCTGCAGG	5253
rs112136670	snp	C/G	0.0221141	0.102801	intron-variant	PHF2	GRCh38.p7	9:93604058	CTCTGCTGAGTTGGG[C/G]AGAGTCCCAGCTTCT	5253
rs112189900	snp	C/G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93605464	CATTGCAATGTAATA[C/G/T]AGAAGAGTTTCATCT	5253
rs112211571	snp	A/G			intron-variant, synonymous-codon	PHF2, LOC107987098	GRCh38.p7	9:93671373	TGTACCTACATCCAC[A/G]CCCACACCTGCATCT	5253
rs112234118	snp	C/T	0.0248432	0.108648	intron-variant	PHF2	GRCh38.p7	9:93648009	ACTCGATAATATTAA[C/T]AGTAATTCCTTGGTG	5253
rs112254982	snp	C/G	0.00279162	0.0372561	intron-variant	PHF2	GRCh38.p7	9:93647606	ATTTTAAAAGGAATT[C/G]TGATCAGGCATGGTA	5253
rs112259060	snp	C/T	0	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671060	AGGTGCAGGTGTAGA[C/T]GCAGGTGGGGGTGCA	5253
rs112310903	snp	A/G	0.0314385	0.121371	intron-variant	PHF2	GRCh38.p7	9:93625775	GAGTCACAATACACA[A/G]TACCTATTCTTAATT	5253
rs112327078	in-del	-/CACA	0.498927	0.0231381	intron-variant	PHF2	GRCh38.p7	9:93663767	ATGCACTCTGCATCT[-/CACA]TCACACACACCACAC	5253
rs112351347	snp	A/C	0.5	0	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668835	TGAGGCCGCCGGCCC[A/C]CCTCAGCCCGCTGCA	5253
rs112367648	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93577691	ACATGATCTTATGCT[C/T]CCTAAGGAAGATGGG	5253
rs112401922	snp	A/G	0.0777841	0.181223	intron-variant	PHF2	GRCh38.p7	9:93661517	GTTGAATGGATTAAC[A/G]AATGGATGAATAGAT	5253
rs112417547	snp	A/G	0.0614824	0.164198	intron-variant	PHF2	GRCh38.p7	9:93644065	AGCAATGGACAACCC[A/G]CAGACTACACCACTG	5253
rs112456616	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93618885	TCTCTGTGTTTGCAT[A/G]TGTTTGTGTGTGTGT	5253
rs112465137	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93662705	GGATGGATGGATGAA[C/T]GAATGAATGAATAAA	5253
rs112473652	snp	A/G	0.5	0	utr-variant-3-prime	PHF2	GRCh38.p7	9:93678006	GGCCTCTGCAGCTCT[A/G]CTGAGAGCATGAGTC	5253
rs112499459	snp	C/T			intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93670592	AAGAGGCCAGGGCTG[C/T]ATCCCATGGGAGGGC	5253
rs112543973	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93617237	TAGGAGGCTGCACCC[C/T]GTAGCCTGCAGCAGG	5253
rs112570997	in-del	-/GTCCGG	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93644956	GGACAGGATGCTCTT[-/GTCCGG]GTCCTTGGGTTGTCA	5253
rs112598288	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93604859	TTTAGCATTTCCTTC[A/G]TGAGATTTTCCCATC	5253
rs112657980	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93592363	TCATTTGGGGAGCGC[A/G]GCATCATTGCCCCCA	5253
rs112732871	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93675344	ACCTTTGTACCGGAG[A/G]CACCCACTTGATGGT	5253
rs112791771	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93653898	ACCTGGATCTGGGGG[C/T]GGGCAGGTGCACATG	5253
rs112837955	in-del	-/A	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93649320	GGTATCAGAGTCTGG[-/A]ATACTGCACATGGCA	5253
rs112948912	snp	A/G	0.5	0	intron-variant, missense	PHF2, LOC107987098	GRCh38.p7	9:93671832	CAGGTGTAGATGCAG[A/G]TGTGGGTGTGGGAGT	5253
rs112999440	snp	C/T	0.0562307	0.157967	intron-variant	PHF2	GRCh38.p7	9:93625666	TATTTTTGGTGGAGC[C/T]AGGGTTTTGCCATGT	5253
rs113068340	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93614879	TGATGGTGACAGTGA[C/T]GGTGATGGTGATGGT	5253
rs113129271	snp	A/C/T	0.012434	0.0778628	intron-variant	PHF2	GRCh38.p7	9:93656033	TGAGGTAGTGCCTGC[A/C/T]GCGCTGTCTGCCCTC	5253
rs113154775	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93669382	GGCAGGAGTGACTGC[A/G]CTCACTTAGGCAGGC	5253
rs113231739	snp	A/G	0.000399281	0.0141238	intron-variant	PHF2	GRCh38.p7	9:93637593	GTGTGTTCAAGGGTC[A/G]TCTGTGCTGTGGCAT	5253
rs113246174	snp	C/G	0.112983	0.209108	intron-variant	PHF2	GRCh38.p7	9:93650576	TGTCGTCAGCCCTGC[C/G]GTCACTGGGTGGGGC	5253
rs113247284	snp	G/T	0.0043584	0.046478	intron-variant	PHF2	GRCh38.p7	9:93676572	TGTGCGTCTGAGGCT[G/T]CCCTGCATGTTTTGT	5253
rs113300403	snp	G/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93585997	AATGGTGCAGACTGA[G/T]TTAGGGGTTTAGGCC	5253
rs113405501	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93639052	AAGTTTGTTTTGATC[A/G]TTCTAGGTCCCTTGT	5253
rs113409787	snp	A/G	0.0244538	0.107838	intron-variant	PHF2	GRCh38.p7	9:93647123	GCCTTGTGTACCCCA[A/G]CTGTAATGTTCATGC	5253
rs113437268	snp	G/T			intron-variant	PHF2	GRCh38.p7	9:93618895	TGCATATGTTTGTGT[G/T]TGTGTGTATGTGCGT	5253
rs113555594	snp	C/G	0.0402882	0.136092	intron-variant	PHF2	GRCh38.p7	9:93657084	CCGCCCTTTTCTGTC[C/G]CAGGTCCTGCCTGGC	5253
rs113567905	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93587581	GGAGTCCTGGGTGAG[A/G]GATGATGGAGGAGCC	5253
rs113617877	snp	C/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93665120	CAGGGAGACAAATTA[C/T]ACACTGTTTCTTAGA	5253
rs113617970	snp	C/T	0.0418186	0.138422	intron-variant	PHF2	GRCh38.p7	9:93596999	GCAGTGGCACGATCT[C/T]GGCTCACTGCCAGCT	5253
rs113618768	snp	A/G	0.0130921	0.0798413	intron-variant	PHF2	GRCh38.p7	9:93625798	TCTTAATTCTTTTGG[A/G]TATGTATCTGTCAGT	5253
rs113724280	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93655720	TGGAGGCTGGGGTTG[A/G]GCCAGAGCCAGAGAG	5253
rs113741585	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93647350	ATGCGGGTGGGGCCT[A/G]GTTTTTCCCCTGGCC	5253
rs113746371	in-del	-/T	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93583827	CTTTTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	5253
rs113760751	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93637659	ATATTTCATCGTATA[A/G]ATATCCACATAGGTA	5253
rs113788394	snp	A/G	0.00199481	0.0315187	intron-variant	PHF2	GRCh38.p7	9:93620219	TCCCAGGAGGGAGAG[A/G]CCCACCTTCTGTCTT	5253
rs113805186	snp	A/C	0.00478085	0.0486577	intron-variant	PHF2	GRCh38.p7	9:93610115	GCTTGGTATCTTTTG[A/C]GCTTCCTGGATCTGT	5253
rs113907105	snp	A/G	0.5	0	intron-variant	PHF2	GRCh38.p7	9:93632639	ACACTAATCCCATTC[A/G]GGAGGACTTTACCCT	5253
rs113908100	snp	A/G	0.21303	0.247251	intron-variant	PHF2	GRCh38.p7	9:93630157	TGGGCCTGGGCCCTG[A/G]GTTGCTGGGGGCAAA	5253
rs113923479	snp	C/T	0.5	0	synonymous-codon	PHF2	GRCh38.p7	9:93676701	CACCACCTCCACCTC[C/T]ACCACGCCAGCCTCT	5253
rs113942376	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	PHF2, LOC107987098	GRCh38.p7	9:93665654	GCTGTGGGGCTATGT[A/G]GATGCTGCTGACCCA	5253
rs113951079	snp	C/G	0.5	0	intron-variant, downstream-variant-500B	PHF2, LOC107987098	GRCh38.p7	9:93673979	CAGGCCTCAGCTCAG[C/G]AAAACCCTCGGCCTC	5253
rs114038058	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93614229	CACAGGCTCTTTAAG[C/T]AGCACAGGGTGGACC	5253
rs114141091	snp	C/T	0.0558544	0.157504	intron-variant	PHF2	GRCh38.p7	9:93634936	GCATGTGCCAACCTA[C/T]ATCCCACAGCCACCC	5253
rs114150377	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93590148	GTTGTACTGATTTCT[C/T]TACACACTGGGCAAC	5253
rs114182087	snp	A/G	0.00835141	0.0640778	intron-variant	PHF2	GRCh38.p7	9:93650738	CCACCCCTCACCCCC[A/G]CTCCATCACATCACC	5253
rs114226655	snp	A/G	0.02016	0.0983543	intron-variant	PHF2	GRCh38.p7	9:93585262	GCGTTTTCCATACAT[A/G]TGTAAGACCTCTCTC	5253
rs114238172	snp	C/T	0.0562307	0.157967	intron-variant	PHF2	GRCh38.p7	9:93639752	ATTACTTGCTGCAGA[C/T]GTAAACTCAGCAACA	5253
rs114264295	snp	A/G	0.0267878	0.112589	intron-variant, utr-variant-5-prime	PHF2, LOC107987098	GRCh38.p7	9:93668511	GGGGTCCTGGGGGTT[A/G]GGGGTGTCTGAGGCC	5253
rs114306260	snp	C/T	0.112983	0.209108	intron-variant	PHF2	GRCh38.p7	9:93651573	GCTGTCTGGGGTAGC[C/T]CTTGGGGCCTGCTGC	5253
rs114376448	snp	A/G	0.00835141	0.0640778	intron-variant	PHF2	GRCh38.p7	9:93581383	TCAGAACTGACAGTT[A/G]AATCCTAGAACCTCA	5253
rs114383509	snp	C/G	0.00676609	0.0577691	intron-variant	PHF2	GRCh38.p7	9:93614603	GGGGTCTCTTCAGCT[C/G]GCAGTCCTGGAGGAA	5253
rs114492208	snp	A/G	0.0103295	0.0711199	intron-variant	PHF2	GRCh38.p7	9:93664086	AGGCCGTGGGACTCC[A/G]TGAGTGTTAGATGTT	5253
rs114579068	snp	A/G	0.0158469	0.0875917	intron-variant	PHF2	GRCh38.p7	9:93586691	CAAGAGGTTTGCCAC[A/G]ACTGGGCTTGGTTCC	5253
rs114579875	snp	A/C	0.00755907	0.0610114	intron-variant	PHF2	GRCh38.p7	9:93631330	TCTCGACCCTATCCC[A/C]AGCACAGCCTCAACA	5253
rs114689898	snp	C/T	0.0267878	0.112589	intron-variant	PHF2	GRCh38.p7	9:93658412	CCTTTGCCCCAGACA[C/T]CCCATGGGTCCGTCC	5253
rs114708009	snp	A/G	0.0115144	0.0749975	intron-variant	PHF2	GRCh38.p7	9:93614163	ACTTTGGCTTACAGG[A/G]TGGTCACCCACTTGT	5253
rs114765798	snp	C/T			intron-variant	PHF2	GRCh38.p7	9:93620569	CCACAAGCACGTGGA[C/T]ATCTGGGAATTGCCC	5253
rs114765802	snp	A/C	0.0379877	0.132479	intron-variant	PHF2	GRCh38.p7	9:93605668	AATCACGTAGTATGT[A/C]GGCTTTTCACTTGGG	5253
rs114768341	snp	C/T	0.0119091	0.0762411	intron-variant	PHF2	GRCh38.p7	9:93584410	TTGATCCATCTTCTG[C/T]TTATTTTTGTAATGA	5253
rs114771476	snp	A/G	0.0295035	0.117819	intron-variant	PHF2	GRCh38.p7	9:93662495	TGGATGAATGGGTGG[A/G]TGGATGAATGGGATG	5253

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