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
rs240585199	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48864737	CTTCCTCCTCACCAC[A/G]ACCTCTTAGAGGTGA	18676
rs240599552	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48858133	TCCAGGTCTGACACG[A/T]GCATACCCAGAGCTG	18676
rs240642088	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48851831	ACTTAGAAGAGCCCA[C/T]ATCTGTGAGCAGTCA	18676
rs240664655	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48812631	TGTGGCCAACCGGAG[C/T]GAGCAGGGTTGACCG	18676
rs240674341	snp	G/T			intron-variant, upstream-variant-2KB	Phf2, LOC102642832	Mm_Celera	13:48869969	TGTCAAAACTGGGGT[G/T]CCTCTGCCTGAAGCA	18676
rs240689521	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48835016	CTGAGCCCCAAGCTC[A/T]CACTTAACATAGGCT	18676
rs240743320	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48820972	TCTAGGTTATCCCAG[A/G]GGGATGGAGGTGGGG	18676
rs240743377	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48829181	CAGCAGAGCTCTGCC[A/G]TGTCCCTGCATGCTG	18676
rs240752911	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48803715	GGAGAAATTCTTTTT[A/T]AAAAAGACCAAGAGT	18676
rs240789106	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48840571	TTGCACCAGCTATGG[C/T]CAGTATTTTACACTG	18676
rs240801192	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48821979	ACAAGGCTCAGGTGA[C/T]ATTAGGGAGTAGAGT	18676
rs240803818	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48849549	AACATGACAGAAATT[C/T]GATCCACAAGACAAC	18676
rs240835248	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48827813	TTCAAGGTTTCTCTG[-/T]TCTTTGCTGCTGCAC	18676
rs240849112	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48855074	CTCCTAAAATGAGGA[C/T]ACTCTGAGCTAAAGC	18676
rs240863252	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48862618	ACAGGAATAAAAAAA[A/C]CAATAGGAATTTTTA	18676
rs240867539	in-del	-/ATAT			intron-variant	Phf2	Mm_Celera	13:48830174	TACATACATACATAC[-/ATAT]GGGCAAAACACTCGT	18676
rs240867557	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48861067	AGTCAAAGGCTTAGA[C/T]ACCACAGAACATGGC	18676
rs240888638	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48822681	GGAGTGGTTTCTGGG[-/A]AGTCTTCCCAGCACC	18676
rs240909939	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48865521	ATGATGTCACAGAAG[G/T]TAAGAACACAGGTTG	18676
rs240914786	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48853670	ACAGCAAACAAACCT[C/G]ACTGGAGAGCAAATG	18676
rs240917822	snp	C/T			synonymous-codon	Phf2	Mm_Celera	13:48820585	GAAGGCCAGGCAGTC[C/T]ACGGGGGTGAGTGTG	18676
rs240975544	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48813155	AGTTTAAAGAGTTCT[A/G]TACTAATGACTGCTA	18676
rs240976653	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48837536	AGAAAACAAAAGAAC[-/A]CACAACTCTTATTAA	18676
rs240976659	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48859875	ACAGTTTGGGCAGCC[C/G]TTCTCCGTGTCCTGC	18676
rs241102829	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48826975	GTCGGGAAAAGTTGA[C/G]GCTCGTCAAATAGCT	18676
rs241111568	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48826017	GACATTGGCTTTGAG[C/T]CGAACCTGCCAACCA	18676
rs241112970	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48817446	CAGCTGTCCCTCTGG[A/T]CTGGCCCAAGACAGG	18676
rs241157682	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48850345	ATTTCTGTATCAGAT[A/G]TGCAGAAGAGCATGG	18676
rs241209211	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48849463	CACCAGATAGAACTG[A/G]GTCCTGTTCCTGGGC	18676
rs241211081	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48819914	GTGGATCAGAACTTA[G/T]ACCAACCCCCCAGAT	18676
rs241261156	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48848325	TATAAATTCAAAATC[A/G]GTCTATAACTTGTCT	18676
rs241262636	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48817097	TTAGCTGCAGGGGTG[A/G]GTTCTAGTACTTCGG	18676
rs241264008	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48808942	ATGAAGGACTGACCA[C/T]AGGGCTCCATCTGTA	18676
rs241315685	snp	C/T			synonymous-codon	Phf2	Mm_Celera	13:48826189	ATCCACACTCCTCTC[C/T]GGCCCTGGGGAGGAA	18676
rs241320597	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48809617	CTTCTCCTGAGACCC[C/T]TTTACTTTCCAGCGT	18676
rs241343762	snp	A/C			upstream-variant-2KB	Phf2, LOC102642832	GRCm38.p3	13:48871032	GGGGGCCCGGCCGCG[A/C]GCGGGACACAAAGCG	18676
rs241410491	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48825376	TGGGTGTGTGTGAAC[C/G]ATAAGACAGGCATCC	18676
rs241441158	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48809419	GCCCAGGTAGAGAGC[A/C]GACCATGAAGACCTG	18676
rs241528866	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48839640	AAACAGGTTTGTACA[A/T]CAGAGAACGCCGTTA	18676
rs241578697	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48816418	GCGCCCTGGCACAGG[C/T]CCACACCCACCCTCA	18676
rs241609259	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48811235	CACATGTGGGGTCTG[C/T]AAAGCACTCTCCCCA	18676
rs241691238	in-del	-/ACACACACAC			intron-variant	Phf2	Mm_Celera	13:48830132	CATAATTTTTATTAT[-/ACACACACAC]ACACACACACATACA	18676
rs241704904	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48834137	GCCCAGGAGTCAGGA[G/T]CACCCACCCCACGTA	18676
rs241775006	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48865059	CATGCAGCGTTAGAC[A/C]GTAGCCTGGTTCAAC	18676
rs241831096	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48822613	TAGCTCCCCCTTTGC[C/T]TCAGTGGTGAGCCCC	18676
rs241872222	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48830484	AGGTAATCCTCTGGC[C/T]TCCCAATGCAGGTGC	18676
rs241892297	snp	C/G/T			intron-variant	Phf2	GRCm38.p3	13:48844104	AAATCTTGCAAGCAT[C/G/T]GAGAGTACGTGGCAA	18676
rs241908871	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48823649	TTGACATAAGCCGGA[A/G]TCATCTGAGAAGGGA	18676
rs241946298	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48837901	GGAAGAGCCACGTGA[A/T]CACCTCAACCCATAC	18676
rs241970790	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48854771	GGGGTTAAGAGCACA[A/T]ATTCTCTCAGAGGCC	18676
rs241982851	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48815720	TTGGAGGATATGATG[C/T]AATGTGTGTGTGTGT	18676
rs242009860	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48806192	TCTGGAGGCTGCTGC[A/T]GCAGCAGCGAGTGAG	18676
rs242180928	in-del	-/ACTACCC			intron-variant	Phf2	Mm_Celera	13:48818287	TGGTCCTAGGGTCCC[-/ACTACCC]TGGCATGGCCTTACC	18676
rs242194889	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48829089	TGATTCCAGTAATCC[A/T]CCCTGGAAGCAAGAC	18676
rs242206287	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48840887	GGAGTCTGTGCAATG[G/T]GTCTGACTCTGACTT	18676
rs242282921	in-del	-/GTCG			intron-variant	Phf2	Mm_Celera	13:48845858	AGAGAATGGAGCTTA[-/GTCG]GTCACGTGTCACACG	18676
rs242410927	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48865437	GGACATTCTTCCCAC[-/T]TTTTTCCAGAACTTT	18676
rs242452243	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48827663	GATAAAACCCAGGAC[C/T]TTTATCATGTAAATA	18676
rs242508489	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48838921	TGTATACATGTATGT[C/T]GATGCCAGGGCAGGA	18676
rs242590897	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48838846	TCCTGTGTGTGTGTG[G/T]GTGGGGGGGTGTGTT	18676
rs242604742	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48836594	GGAAATGATGCACAA[A/G]GCTGACCTCTGCAAA	18676
rs242664593	in-del	-/GAAG			intron-variant	Phf2	Mm_Celera	13:48839156	ATTAGAAGAAAGCAT[-/GAAG]GAATGAACTCCTCAA	18676
rs242683112	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48832642	ACCACAGAAGGCACT[G/T]CCAGGCATGTCCAGG	18676
rs242721418	in-del	-/AGAGAGAG			utr-variant-3-prime	Phf2	Mm_Celera	13:48801926	AAATTAAAAAGAGAA[-/AGAGAGAG]AGAGAGAGAGAGAGA	18676
rs242890819	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48836444	TACAAGACGGTGGCA[C/G]GTGCCTACTGTCGCA	18676
rs242947210	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48866103	CCCTGCCTCACATCC[A/G]CCCCAACAGCAGCCA	18676
rs242972655	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48848133	TTAAAAAAAAAATTT[A/T]AACTAAGAATGGCTT	18676
rs243001930	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48864921	CAGGATGGCACTCCA[G/T]AGTCCCACAGGCATT	18676
rs243027361	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48838280	ACAGCCAGGATGGCC[A/G]CTGCTGTCTTCTACT	18676
rs243028455	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48845422	CTGAGTCAGTAACTG[C/T]GCTGCTGTGATAAGA	18676
rs243042596	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48829290	CCACCCCCCACCCCC[A/C]CACACACATTTTTTG	18676
rs243086751	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48844854	AAAGTAATGCCGGGC[A/G]TGGTGGTGGACGCCT	18676
rs243087641	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48817407	CCCTTCCCAGTAACA[A/C]AGGAGAGCAAAGAGG	18676
rs243090045	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48815436	ACAGTGGTGGTGAGC[A/G]AGATCACTGTCTCAG	18676
rs243139132	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48808663	CTATACCTACACCTA[C/T]ACCCTCACCTACACC	18676
rs243183537	in-del	-/GGGACGT			intron-variant	Phf2	Mm_Celera	13:48842009	CACAGGCACCTAAGA[-/GGGACGT]GGGTTTAGCCCTGAA	18676
rs243204039	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48840035	AACATAAAATGAAAT[A/T]CAAGCCAGCAGTCTC	18676
rs243229482	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48857593	AAAGCACTTTCATGC[C/T]CTCAGTACCCTAACA	18676
rs243329714	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48842183	CTGGCAGCTAACAGG[A/G]TGTTGCAGATCCTGC	18676
rs243347851	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48811958	CAGAGTCAGGGTGAG[C/T]GGCTGCCTCGGGCAG	18676
rs243357321	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48830214	ATAAATCTAAAAGAA[-/T]TTTTTTTTAAGTGTG	18676
rs243386131	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48841536	AAATAAAAAAAAAAA[A/G]GTAGAAAAATCACAC	18676
rs243410860	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48812561	CCTGTAATGAGATCT[A/G]AAGACAGCTACAGAA	18676
rs243465146	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48857294	CCCCACCCCCGAACA[G/T]TCTGCAGTCCAGAAC	18676
rs243466158	snp	C/T			utr-variant-3-prime	Phf2	GRCm38.p3	13:48802283	AAGTAACTGCATCCC[C/T]GACCCTCGCCATACA	18676
rs243474230	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48834909	TGTAGGGGTGTTAGG[C/T]GGGATAAACCAAGCT	18676
rs243517395	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48833250	ACACAGGCACCCTCT[-/G]CACAATCACTCCCCA	18676
rs243529078	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48868443	CCTGCCTTCAACCTC[C/T]CTGGTGCTTAGATTA	18676
rs243531549	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48840395	TTTGCAGGTTGATTT[A/G]AAGTGATTTTATGGA	18676
rs243531633	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48834381	CTTCAGCTCTTTCTG[C/T]TCATAGGTCTTAGTC	18676
rs243555674	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48816808	CAATAACACATCCAC[C/T]CCTCTGTCCCTCCTT	18676
rs243580458	in-del	-/GGG			intron-variant	Phf2	Mm_Celera	13:48848538	AAAGAAGAGAAGGGA[-/GGG]AAGAAAAAGAATTCT	18676
rs243602654	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48861776	GGAGGGTCTATGGGG[C/T]TTGCCAGCCAGTCGG	18676
rs243653725	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48845484	TTACTTGGTGTACGG[A/T]GGCTCCAGAGGGACA	18676
rs243673457	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48809947	CCAGCACAGTACCCT[C/T]TCCCGCACAGTACCC	18676
rs243704611	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48832318	CCATATGAAGAACTG[C/T]CACCTTCCTGCCAGG	18676
rs243721864	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48808415	CCATCGACACCCACA[C/T]GCTCACCAAGCCCAC	18676
rs243733407	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48841140	AGAAGCAGCGGTGCC[A/C]CTCCCAGGGGAAGGG	18676
rs243734352	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48810719	TGGGGACTTCACTGA[A/G]CATGGGCAGGAACAA	18676
rs243761846	in-del	-/GC			intron-variant	Phf2	Mm_Celera	13:48835831	ACAGAACCCAAGGAT[-/GC]GCGACCCACAACACC	18676
rs243787765	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48809051	CCTCATCTCCCCCAG[A/G]GTACACTGGTGCCCT	18676
rs243879389	snp	A/G			synonymous-codon	Phf2	Mm_Celera	13:48805874	CCTCTTCTTTGACCG[A/G]GACTTGAAGACGGGG	18676
rs243931955	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48813674	AGCGCGCTGCAGGCC[C/G]GGCTGTGGGAAGGGG	18676
rs243980841	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48836740	ACCAAGATAAAGAGA[C/G]AGGACCTGAAGATTA	18676
rs244019232	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48850584	AGTGAGACTAGCTAT[A/G]AATCTAAACTCTCAT	18676
rs244044581	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48805771	CCCAGGAAATGCCTA[A/G]AGCCATACCTATGTC	18676
rs244101372	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48806589	ACCTCTGGCTATCAG[A/G]AAGGCCCTGGACTAA	18676
rs244221721	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48826920	CACTGATCAATTGGC[A/G]ACTACTCAGGAAATA	18676
rs244233184	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48818941	GAAGAGCGAGAGCCA[C/T]AGTAGGAAACAATAT	18676
rs244277058	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48859549	TTAGAGTATTGGGCC[A/G]GGGTCTTTGCTACAG	18676
rs244310080	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48811608	ACCACCAGAGACTGT[A/G]TGACACCCTGCACAG	18676
rs244373944	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48839762	AGCTCAATAATAAAA[C/T]CATCTAGATTTTAAA	18676
rs244653358	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48822788	ATGTATGTCACTGGT[C/T]CCAAGTGCTCCTTAT	18676
rs244681349	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48844171	ATCCTGAGCCCAGCA[-/T]TTTTTAAGCTTTGCA	18676
rs244689035	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48857982	TGGATGTCCTGGAGC[A/G]GGAGTTATAAGTGAT	18676
rs244733124	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48815160	CCAAATCTACACATC[C/T]CTCCCCATGGCATCC	18676
rs244740819	snp	C/G			intron-variant, upstream-variant-2KB	Phf2, LOC102642832	Mm_Celera	13:48869272	TGGATGCCAGTTGGT[C/G]GCTGTTTATAGTGGC	18676
rs244743880	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48833375	ATATGCCTTCCCCAG[C/T]GGATAGGTTGTTGAC	18676
rs244789432	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48861115	ACACATGAGTGGAGA[C/G]AGATGCAGTGTTCAT	18676
rs244795255	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48868016	GAGGAGGGAAACCTG[A/G]CTGAAGAAGCTGGCA	18676
rs244797757	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48842969	ACACACTTTACCAAC[C/T]GAGCCATATTCCTCC	18676
rs244806522	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48819708	TTCCAGAGGCCACTG[-/C]CCCCCAGACCACTCG	18676
rs244827101	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48825524	GAGTGTAAGTGGGTG[C/T]GCGCATGGTCTGTGT	18676
rs244847613	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48860031	CTAGTTTAGCTCAGG[A/G]CTTGGAATCCCTGGA	18676
rs244880230	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48838211	CAGGAAAAACTCACA[A/G]CTAATATTACACAGG	18676
rs244883209	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48826231	ACATGCCGGGAAAGC[A/G]CTATGGCCTCCCTGG	18676
rs244887445	snp	A/C/T			intron-variant	Phf2	GRCm38.p3	13:48816382	CACAGACTTTCCTCG[A/C/T]AGCTCTGGGGACAGG	18676
rs244956285	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48844788	TCTTCAAAGAGAAAA[A/G]GAGTTACAAAGGCTA	18676
rs244957152	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48864982	CTCACGGCCCAGCTG[A/G]TAGACTTGTTTTACC	18676
rs244961656	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48808863	CTCTATCTGTATCTA[C/T]ACATCTCTTGGTTAG	18676
rs245051057	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48868977	AAATCAAAATCCTCA[A/G]AGAAACAGTAAGGTG	18676
rs245064530	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48837856	CAGCCGCCATCCTTC[C/T]TCAGACGTTCTTACC	18676
rs245123468	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48829379	CTGTAGAAACTCACA[A/C]GCTGATCCTAAAATC	18676
rs245147563	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48856513	TTTTGCATGCTTGGG[A/G]CCTGATGGCACTTGC	18676
rs245178629	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48822300	GTAATAAAAAAAATG[C/T]AGACTACCACCTAAC	18676
rs245217909	in-del	-/TA			intron-variant	Phf2	Mm_Celera	13:48859016	CCCAGGGGGCGGTCC[-/TA]TATAGCACCTGTCAC	18676
rs245247115	in-del	-/AAG			intron-variant	Phf2	Mm_Celera	13:48863033	GTATGAAATTCTTCA[-/AAG]AAGTCACTAGAGTAA	18676
rs245321236	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48831066	GACGGCTGACGTACA[A/G]TGCAGTGGGCCTTGA	18676
rs245339963	in-del	-/CTC			intron-variant	Phf2	Mm_Celera	13:48839164	GAAAGCATGAATGAA[-/CTC]CTCAAGCCTTTGGAT	18676
rs245344959	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48853223	ATTTTAAAATTTGAA[A/C]CTGTTTTAACTAATT	18676
rs245357200	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48806416	TGGTGATTCTGTGGG[C/T]AGCAGCAGGACCTGG	18676
rs245373750	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48828462	ACTACTTAGAGAGCC[C/T]CACCTCCACTCCTGC	18676
rs245374778	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48838374	TAGAAAGAGGTGATG[C/T]GATCTTTATTTGCAG	18676
rs245381097	in-del	-/GACA			intron-variant	Phf2	Mm_Celera	13:48860292	CTATGGCAGGGACCT[-/GACA]GACATACCTGCTGCA	18676
rs245403409	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48827114	CAAGGCGGAACCTGT[C/T]GGAACATCTGTGGAC	18676
rs245425627	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48828986	GCCTCAGTGTCCCTG[A/G]CCACATGCCTCCCAG	18676
rs245435710	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48834966	CACGTATGGGGCTTG[C/G]CTGAGCTTGGGGCCT	18676
rs245449234	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48820679	AGCTTTCACCTCCCC[C/G]ACTCACTCACCCCAG	18676
rs245462501	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48827872	TGGGGATTCCCTGCC[A/G]CTGGCTTCCATTTTC	18676
rs245531484	snp	A/G			utr-variant-3-prime	Phf2	GRCm38.p3	13:48803514	CTCCCTGGGCCAGGC[A/G]GCACAGCCACCGTCC	18676
rs245575063	in-del	-/GG			intron-variant	Phf2	Mm_Celera	13:48868653	CCAAGAATAACTGGA[-/GG]GGGAGAGACACACAG	18676
rs245584540	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48804290	CCAGAATCCTCTTTG[C/T]AGTGTGCTCTCTAAG	18676
rs245654212	in-del	-/GG			upstream-variant-2KB, nc-transcript-variant	Phf2, LOC102642832	Mm_Celera	13:48872228	GGGAGATAGGAAATT[-/GG]GGGGCGGGGGGCGCA	18676
rs245660448	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48864807	GTCAGGAAAGCCGAC[-/T]GTGACAGAGACTTGC	18676
rs245741286	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48840001	CACAGGAAAAAAAAA[-/G]TGATTTCCTCAGAAA	18676
rs245761901	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48824542	TCAGTCACCGCCAGG[A/G]AACCCATGCCTTCCT	18676
rs245876166	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48815079	GGAACCAAGACAGCA[G/T]GGCCATGCTGAGGCT	18676
rs245982873	in-del	-/CACACA			intron-variant	Phf2	Mm_Celera	13:48862804	ATGATAGTGTGCACG[-/CACACA]CACACACACACACAC	18676
rs245986187	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48818194	AGCCTGGACCTGAGG[G/T]TCTCCATCCTTCTCC	18676
rs246037381	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48844909	AGGCAGGTGGATTTC[C/T]GAGTTCGAGGCCAGC	18676
rs246115860	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48856399	ATAAACATTCAGTGA[A/C]ACTGAGTGCTGTGCA	18676
rs246149599	in-del	-/AGA			intron-variant	Phf2	GRCm38.p3	13:48846248	AGGAGGAGGAGAAGG[-/AGA]AGGAGGAGGAGGAGG	18676
rs246166509	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48844996	GGAAAAACAGTCTTT[A/G]AAACTTTCAAACCCT	18676
rs246260028	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48840353	TGGCAAGTGGGGTGC[C/T]AGTGGTGGGAAAAGG	18676
rs246358572	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48810572	CATAATGGCAGGCCA[A/G]GTCACACATCCCTGA	18676
rs246407349	in-del	-/ACACACACACACAGAC			intron-variant	Phf2	Mm_Celera	13:48862345	GTTGTCCTCTGACCT[-/ACACACACACACAGAC]ACACACACAGACACA	18676
rs246407733	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48835657	AAGGACAGAACATTC[-/T]CTCAAAGCCTGGAGA	18676
rs246523008	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48841435	CAAATCCCAGCAACC[A/C]CATGGTGGCTCACAA	18676
rs246551931	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48852049	CAGGTGGTGCTTAGC[A/G]TATCCACACCTGACT	18676
rs246619122	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48864134	AGATAAATCCATGGG[A/G]CCAGAAGGGGATGGG	18676
rs246676398	in-del	-/ACGAAC			intron-variant	Phf2	Mm_Celera	13:48850814	AGCCGAAGGCCAGGA[-/ACGAAC]ACACACACACACACA	18676
rs246687504	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48862489	GATTCCAGCACTCAG[A/G]AGGCAGAGCCAGGTG	18676
rs246721618	in-del	-/CTGTCTGT			intron-variant	Phf2	Mm_Celera	13:48828308	CAGCCAGTGCACAGG[-/CTGTCTGT]CTGTCTGTCTGTCTG	18676
rs246814615	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48836302	AAAAATGTATGGCCT[C/T]ATGATATACTGCATG	18676
rs246850901	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48833092	GGAAGAAGCCATAGA[C/T]GCTAGCATGCACTTG	18676
rs246885249	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48842052	GTCAAAGGTGTAGCT[C/G]TGAAAAGACCATTCT	18676
rs246911676	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48826267	ATGGTGGGGTGGACA[A/C]TGACCTGTCCTCGGC	18676
rs246922147	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48839320	GGTCGTCCTGGATAG[A/G]GGCGGGGCTCATAAA	18676
rs246942699	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48840575	ACCAGCTATGGCCAG[C/T]ATTTTACACTGGCCA	18676
rs246942975	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48851095	CATAAAAACCAGGCA[C/T]GGAAGGGGCACATCT	18676
rs246946574	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48847146	GAAAAGTGAAAGCTG[C/T]CAGTCTAAAATGTCT	18676
rs246972915	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48818610	TCAAGATGGCCTCCC[A/C]TGAGGCCACCCCTAG	18676
rs247007196	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48849950	AATATATACACCACA[C/T]ATATCACACATAAAA	18676
rs247011049	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48858949	GCTGCAAGGTCAGGG[C/T]AGCATTAGAGGTGGC	18676
rs247016864	snp	A/G/T			intron-variant	Phf2	GRCm38.p3	13:48846160	GCAAGTGCAGGCATC[A/G/T]CTTTAAATAGTAGTG	18676
rs247036346	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48819204	GCAGGGTGGCAAGAG[C/T]CACAACTATATCCCT	18676
rs247037199	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48840280	CTAACATACAGGGCC[A/G]ATATTGCAGAACAAC	18676
rs247047394	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48819768	TGGGGTGCCCACCCA[C/G]CCAGCACCTGCCCTA	18676
rs247091057	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48837918	CCTCAACCCATACAG[-/A]AAAAAGCACTGGGTA	18676
rs247113153	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48829833	TGGATTTGGTAAAGG[G/T]TTTAGATTGCAACAA	18676
rs247126016	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48812248	GCTGTCATGAGACTA[C/G]AGAGCTGAGAGGACA	18676
rs247139767	in-del	-/GT			intron-variant	Phf2	Mm_Celera	13:48818839	ATGATTCCCTACCTG[-/GT]GCCTCTGCCTCAAGG	18676
rs247177244	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48864533	AGAAGTCACCAGAAA[C/T]ATGGGGACTAAAGAT	18676
rs247274790	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48824079	CAACTTTCTCTTGGT[C/T]ATGGCGTTTTATCGT	18676
rs247298649	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48805035	CCCAGAGGCATTTAA[C/T]GAGGGCATCCTGGGT	18676
rs247308551	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48845906	TAACCCCAGCACCCA[C/T]AGAAAAAGCTGGCAC	18676
rs247310336	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48838489	GGGATGCAAGATTAC[C/T]ACAGCAGCACGGCTG	18676
rs247331171	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48824778	GTCCTGTTGGCCCAG[C/T]CTGAAGATAGGATAG	18676
rs247332220	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48815303	TCAGCATTAGCTCAC[A/G]CCAGCCCCACTGTCA	18676
rs247371164	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48845107	TCTCTCCCACCACAT[C/T]GGGCCCAAGCAGTGA	18676
rs247395185	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48816742	TCCGCCTACCTATCC[A/G]TCTCTATCCGTTTAC	18676
rs247396512	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48815908	GGGGCACATATGTGA[G/T]GTGGGACACTGTATG	18676
rs247397479	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48837504	TATCTTGATTTCAAA[G/T]CCAGACAAAAGCATA	18676
rs247459937	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48808283	TCAGTCCTGGCAAGG[A/G]ACATTCCTTCTCCGC	18676
rs247502949	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48808117	ACACCCAGTCACACT[C/T]CAGGGAGGGAATGAG	18676
rs247542818	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48840966	TTATAGAAAAGCCAA[-/G]CATGACAGGTAGAAA	18676
rs247573584	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48837742	TCTGTGCCCCCTGGA[A/G]GTTACAGGGGAGCAG	18676
rs247638158	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48831364	ACCTCAGGGTGGTCA[-/G]GGGAGCTGAAGGAGA	18676
rs247664906	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48820275	GTCACCCAAAGTGAC[A/C]GCTACCATGGGTGGA	18676
rs247692306	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48809242	ATCCGGCTCTGACTT[-/C]CTCGGGGCCCTGTGC	18676
rs247706777	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48834851	GAAGCACTGGATTCA[C/T]AACAGCAGGCACTGT	18676
rs247715349	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48867780	AAATCAGGCTGGCCT[A/G]GAACTCAGAGATCTA	18676
rs247716354	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48812774	AAGAGTCAAAGGAAG[C/T]CTATCCTTGCTGCTC	18676
rs247718646	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48821125	ATCCTGATTTTAAAG[C/T]ACATACATAATCACT	18676
rs247772532	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48813503	GGAGCCACCCCCTGC[C/T]ATTCCTATGCCAGGG	18676
rs247831154	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48814454	TCAGCTATGGGCTAT[G/T]AGATACTGTGTATCT	18676
rs247844913	in-del	-/ACACAT			intron-variant	Phf2	Mm_Celera	13:48832937	CACACATGCAAATGG[-/ACACAT]ACACACACACAAGGA	18676
rs247883641	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48862117	TGGCCAAGTCACCAC[A/G]TCATAAAACTCAAAA	18676
rs247955393	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48810423	ACAGCCCCACTGAGA[C/T]TGGATAGGCAAGCTT	18676
rs248000827	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48828419	TTCCAGGGCAGCTTG[G/T]TCTACCTAGAGTTCC	18676
rs248200664	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48858561	GGATGGCAGGAGGAG[A/C]CATCTTCCTGGGTGA	18676
rs248257833	snp	C/T			upstream-variant-2KB, nc-transcript-variant	Phf2, LOC102642832	Mm_Celera	13:48872134	AACCCCCACCCTTCC[C/T]AAATAGGTAAACCCA	18676
rs248265322	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48844131	GCAAACTATTTAAAC[A/G]GTTTGAAGATCAGGG	18676
rs248295467	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48824459	TGTGGGACATGCACC[C/T]TACACGTGCAACTTT	18676
rs248360177	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48814327	AAGCATAGCCCACAA[C/T]CCTCTTTTCCAGACT	18676
rs248400587	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48867564	CAACACTCCACCACT[A/C]CAAGCATGGGTGACT	18676
rs248448640	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48805215	TCCTCTTGCACGAAC[C/T]CTTCCTTCTCCTCAC	18676
rs248485620	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48864000	TATTATTCAGCCATT[-/A]AAAAAAAAAATCAAT	18676
rs248541597	snp	C/T			intron-variant, upstream-variant-2KB	Phf2, LOC102642832	Mm_Celera	13:48869970	GTCAAAACTGGGGTT[C/T]CTCTGCCTGAAGCAG	18676
rs248591131	in-del	-/ACACACACAC			intron-variant	Phf2	GRCm38.p3	13:48847854	TATATACACAAACAT[-/ACACACACAC]ACACACACACACACA	18676
rs248601771	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48863242	ACTTGCAAATCAAGC[A/T]TCAGATAGAGGCGGG	18676
rs248670141	in-del	-/G			upstream-variant-2KB, nc-transcript-variant	Phf2, LOC102642832	Mm_Celera	13:48871711	AGCCACAGGACTGCT[-/G]GGGAAGACAAGGGGT	18676
rs248704879	snp	A/G			missense	Phf2	Mm_Celera	13:48817664	TGGGGGGCTTGGGGG[A/G]TTTGGGGGGCTTGGG	18676
rs248766734	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48863655	GAACCAGTCAAAACC[-/A]ACCGCTAAACACAAC	18676
rs248790417	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48807517	GATGGATTTTACAGT[C/T]CTGACTGTAGCTCCT	18676
rs248875702	snp	C/G/T			intron-variant	Phf2	GRCm38.p3	13:48843259	GGAGGCAGAGGCAGG[C/G/T]GGATCTCAGAGTTGG	18676
rs248890135	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48826462	TACACAGATGCTTAG[C/G]CAACTTGAGCTTCAG	18676
rs248906029	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48864311	ACCTTCAAGTGGTAA[C/T]ATCACATGAACTGAA	18676
rs248935109	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48842409	GACATAGGGGAGGGG[C/T]GAGCATGCCCTTCCA	18676
rs248957974	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48860905	GAAATGGTGCTGGGT[A/G]TTGCTCAGTAGTAGA	18676
rs248975043	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48840216	GTTTGTCTTAAAGTT[C/T]ACACATTCAGCAACA	18676
rs248975467	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48847443	ATCAAATGCAGTAGT[A/G]TGTCTGTAACCCAGT	18676
rs248991956	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48852193	CTTAGGGCAGAGGAA[A/G]ATCTATAGGATCCAG	18676
rs249062375	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48866303	GGAGGGAGGGAGGGA[A/G]GGAAGGAAGGAAGGA	18676
rs249070071	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48811457	GGGTGGTACTAGGCT[C/T]ACCCTAGGTTCCAAC	18676
rs249113205	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48811346	TACCCCCATCTGTGT[G/T]CTGTCTCCACGCCAC	18676
rs249143331	in-del	-/ACACACACACACACAC			intron-variant	Phf2	Mm_Celera	13:48808799	ACCATGTACACCTGT[-/ACACACACACACACAC]ACACACACACACACA	18676
rs249204787	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48838901	AGTTTGCAAATGCAC[A/G]CATGTGTATACATGT	18676
rs249215403	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48844183	AGCATTTTTAAGCTT[C/T]GCATGTGCATGCGGT	18676
rs249230914	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48831990	ACCCCGCCCACCTTG[A/G]AAGGTCTGCCCACCT	18676
rs249237380	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48835124	GGCAAGAGTAAACCA[A/T]AAGTCAGTCAGCTGA	18676
rs249278204	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48833796	CCAGCCTCCCGGGCC[C/T]CAGGGACCAGCTCCA	18676
rs249296831	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48840708	GAGCATCCATACCAG[A/G]TATGGAGGAGTCACA	18676
rs249342193	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48839573	GTGTGTGTTTGTGTG[A/T]GTGAGAGAGAGAAAG	18676
rs249355444	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48830541	TATGAGGAAAAAGAG[A/C]TCAATAGATTTCTCT	18676
rs249365213	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48838126	TTCAGAAAAAAAAAA[A/G]AAAAAAAAAAGTCTT	18676
rs249401513	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48839132	CTCTAAGATCTAAAA[C/T]GATAAAGGTATTAGA	18676
rs249462324	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48824861	GATAACACCTGAGAC[C/T]TGCTGGGACCTCTAC	18676
rs249524530	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48822252	ACACACATTATTATT[C/G]CATGACACTACAAAT	18676
rs249528111	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48807158	CCCTCAAAAAGTCAC[A/G]TTATACGATCCATTT	18676
rs249628650	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48831372	GTGGTCAGGGGAGCT[A/G]AAGGAGACGCTCTCT	18676
rs249644499	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48808666	TACCTACACCTATAC[A/C]CTCACCTACACCTAT	18676
rs249706481	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48809239	CAGGATCCGGCTCTG[A/G]CTTCTCGGGGCCCTG	18676
rs249776687	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48829236	GCAGGCAGCGAGACA[C/T]GCTCCTCATGGGTCT	18676
rs249863327	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48806297	CTGCCCAGCAGCCTG[A/C]ATGGCCACTACGGAG	18676
rs249876403	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48838848	CTGTGTGTGTGTGTG[G/T]GGGGGGGTGTGTTTG	18676
rs249909124	in-del	-/AA			intron-variant	Phf2	Mm_Celera	13:48863999	TATTATTCAGCCATT[-/AA]AAAAAAAAAAATCAA	18676
rs249925951	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48815443	TGGTGAGCGAGATCA[C/G]TGTCTCAGAAAAAGA	18676
rs249946085	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48845426	GTCAGTAACTGTGCT[A/G]CTGTGATAAGATGCT	18676
rs249992085	snp	C/T			synonymous-codon	Phf2	Mm_Celera	13:48807693	GGCAGTCCTCTTCAG[C/T]AGGCGCTTGCCTGTG	18676
rs249995285	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48816279	TGAAAGGCAGCGGAG[A/G]AAGACATGGAGACGA	18676
rs250017916	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48861299	GGGGCTAAATACTTG[A/G]TCCCAAATAGCCAAA	18676
rs250058721	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48803839	CCCCATGGACCCAAC[A/G]TGCTCAGAGGTGTAG	18676
rs250125952	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48804735	CTCCTAAGAACAAAG[G/T]ATGGAGGGGTGCGGC	18676
rs250152618	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48813671	CAAGCGCGCTGCAGG[-/C]CCGGGCTGTGGGAAG	18676
rs250185699	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48836872	AGTGTAGGTAAAATG[A/G]ACAAATTTCCTAGGA	18676
rs250224988	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48851979	CTCCTAGCATCTCAA[G/T]TCCTAAAGAAGCTCA	18676
rs250334548	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48812214	CTCAGGTTCCCCAAT[C/T]ATCAAGTTAAAGTCT	18676
rs250406014	snp	A/G			synonymous-codon	Phf2	Mm_Celera	13:48813046	GTCGATGTGCAGAGA[A/G]CCCTCGTCAGAGGAG	18676
rs250418433	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48804130	GCCCTGAGCTGAGAA[C/T]CGGTCCTGTAATCAG	18676
rs250493871	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48863672	CCGCTAAACACAACT[C/T]CACACCCACTCCCCG	18676
rs250530230	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48858336	CCCCAACAGGCAGGG[A/G]ACAGACCCAGGAGGC	18676
rs250539189	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48816150	TAGTGGGTATAACTG[C/G]GGACCAGATCATGCC	18676
rs250597041	snp	C/T			intron-variant, upstream-variant-2KB	Phf2, LOC102642832	GRCm38.p3	13:48870410	GCCTCGTCCGGCTCC[C/T]GGCCTCCGCGGCCAC	18676
rs250619727	in-del	-/GTGTAT			intron-variant	Phf2	Mm_Celera	13:48839552	AGAGATCATGCAACA[-/GTGTAT]GTGTGTGTTTGTGTG	18676
rs250628570	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48827625	CTGTCTCAAAAAACT[A/T]CAAATAAATAAATAA	18676
rs250644173	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48838958	GTGTCTTCTTCTGTG[C/T]TCTCTGCTTTACTGT	18676
rs250653093	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48868836	AGAGCTCTAGCCCCA[A/G]GAAGAGGGGTAACTC	18676
rs250707474	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48845954	ATCCCAACACTGGGT[A/G]GTAGAGACAGGAAGA	18676
rs250813382	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48803808	GCCAGCTAGGCTGAG[-/C]CCGGGTTTAGAAATC	18676
rs250842059	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48844247	CCTGCGGGCTCTGAG[A/C]TGGATCTAAGAGCCC	18676
rs250859237	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48859190	ATTCTCGACTGTCCC[A/G]GGACAGCAAGGGTCT	18676
rs250871393	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48823850	GACTTGAGCCTACAA[A/C]CCTGGTCTAAGGGAT	18676
rs250904466	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48855386	CAAAACCAGGCTACT[A/T]GCAAGGTCCCCAGCA	18676
rs250915212	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48852643	TTTGTTTTGTTTTTA[A/G]CTTTTAGAAACAGAG	18676
rs250971895	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48864431	CAGGCTCTAGTTCCA[A/G]ATAGGTTTTTCTGTT	18676
rs251027384	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48830815	GGATTTTCCATCTGA[C/T]CCAGTGGCTCCACAC	18676
rs251032247	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48863515	TGATAAATAGTAAAA[A/C]TAAAGTAGACAATGA	18676
rs251080610	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48821350	AGGAAGACTTCTGAA[C/T]GACCACCCTTTTCCT	18676
rs251196810	in-del	-/CATACA			intron-variant	Phf2	Mm_Celera	13:48850902	CAGCCGAAGGCCAGG[-/CATACA]CGCACACACACACAC	18676
rs251214945	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48854180	GCTGTGGTGCATGGA[C/T]TTGGGCCAGGACTCT	18676
rs251215645	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48819384	CAATCTACATCTGTC[C/T]GACACCCCTCAGGGG	18676
rs251268085	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48827424	ATATAAGGGACACAC[A/C]AGCCATCCTGTTCAA	18676
rs251284460	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48869115	TGACAGGTAACCAGA[A/G]GTGCTATAGGTCTTG	18676
rs251314908	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48840076	CTATCTATGAGTTAC[A/G]GATTGGCATTCTGTC	18676
rs251339009	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48837344	CACCAACCCTCCTCC[A/G]AAACAAACAGATAGG	18676
rs251395967	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48820519	CAGCACTGTAGGAGC[A/G]ACCTACCTCATCTGC	18676
rs251396843	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48836667	TCCCCGCAAACGTCA[C/T]CAGTAACACCAGAGA	18676
rs251414432	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48855331	TTCCCTGTGTCCCCA[A/G]ATCCAGAGCCCCAGC	18676
rs251438051	snp	A/G			downstream-variant-500B	Phf2	Mm_Celera	13:48801285	TGGCAGAGAGGGCTC[A/G]TTGCTGGCTCCTTGT	18676
rs251442618	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48867257	ATGGCCAAGACACGA[C/T]TGAATGAGGAGTCTT	18676
rs251503137	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48829159	CAGGGACCACAGTGA[C/T]GAGGGACAGCAGAGC	18676
rs251503295	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48865488	TTCCCTGTCTTAAAA[C/T]GATGAGTTGGGGGGT	18676
rs251504535	in-del	-/TG			intron-variant	Phf2	Mm_Celera	13:48838834	CGGGAAAGACTATCC[-/TG]TGTGTGTGTGTGTGG	18676
rs251504859	in-del	-/CACACA			intron-variant	Phf2	Mm_Celera	13:48829658	GAACAAATAGAAAGT[-/CACACA]CACACACACACACAC	18676
rs251539447	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48865600	CAACCATCCATAACT[C/T]CAGTTCCAGGGAATA	18676
rs251541032	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48810145	CCCTCCAGCACAGTA[C/G]TCCCTCTAGCACAGT	18676
rs251562895	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48829531	AGGACAAACACAAAC[C/T]GGCACCTAGAATTCT	18676
rs251629407	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48824397	CTAAACTCCTTCCAC[A/C]CCCTCAATATGACAC	18676
rs251671317	in-del	-/CC			intron-variant	Phf2	Mm_Celera	13:48806257	AAGTCCCAAGACCCT[-/CC]CCCAAGCAGACTGGG	18676
rs251688270	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48824989	CATGTGGCGGGGAGC[A/G]TGTGATGGAAGTGCT	18676
rs251744016	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48834431	GTCTCAGCTTGCACT[A/G]AGCACCAGGGTGAGA	18676
rs251750211	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48816997	CCCTGTCCACAGAGG[C/T]TCAGGCCCTTATAAC	18676
rs251761421	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48848681	GAGGGCCCAGGGTAG[A/G]AGGCTGGCCCAGAGT	18676
rs251818945	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48833888	AGCTTAACAAGGTGC[C/T]AGAGAGCAAGAACAC	18676
rs251829338	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48806495	AGCAGAGCACACTCA[C/T]CAAGGGGCGCAGATC	18676
rs251861494	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48817894	AGGAGAGGGTCATTC[A/G]TGTTCCCTCTAGACC	18676
rs251885722	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48849365	AAAAGCACTGGACAC[C/G]TGCCAGCAACAGAGG	18676
rs251885844	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48861444	CTAAATACCTAGGGA[A/G]TAGAAGTGACGGATC	18676
rs251916360	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48815180	CCATGGCATCCATCA[C/G]TTAAGGCCATAAGCT	18676
rs251967797	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48825923	CAGGCTCACAGCCCC[A/G]GAACCCAGAGCAGGA	18676
rs251969065	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48860753	GTATAGATTGTGTAC[C/T]CAGCATATGGGTGTG	18676
rs251971055	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48806770	CAGAGCCTTGTTGGT[A/T]TCTGATCTCACATAT	18676
rs252030751	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48826694	CCTGGCCTTCCTTTT[A/G]CTTCCTGACTTATGA	18676
rs252133901	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48848449	AAGAGAGCTGGGGAC[A/G]TCGCTCAAAGTGAAA	18676
rs252225924	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48859949	TCTGGTCAGGTAGCT[A/C]CTTCCCTATCCTCAA	18676
rs252258557	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48866823	CCATAAGAGGGTCAG[A/G]GGGTCAGGTTTAAGG	18676
rs252340672	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48808756	TGCACATACCCTCAT[C/G]TACACTTGTACTCAG	18676
rs252398082	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48809378	CTGAGTTGGGGAGTG[A/G]CACAGGATCCCAATG	18676
rs252556228	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48837114	CTCAGTGGGTAAAGG[C/T]GCTCACCACCAGGCT	18676
rs252573709	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48813257	GGTCCTCAAAACCAC[A/G]AAGGTTGAAGTCACC	18676
rs252652945	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48825443	CTAAGACAGGCATCC[A/G]TGAGTGCACTGAGTG	18676
rs252656493	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48843165	TTCAAAGCTATCTGA[A/G]TTTATAAGTATATCC	18676
rs252668070	snp	A/T			intron-variant	Phf2	GRCm38.p3	13:48847878	ACACACAGATTTTTT[A/T]AAAAAATAGGATATG	18676
rs252746548	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48833225	CATTTACGGTGGCAC[A/G]CGAGTAAGAACACAG	18676
rs252753948	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48858481	TCTCCACTCTCCAAA[G/T]AACACTGGTGGGTTC	18676
rs252757280	in-del	-/AG			intron-variant	Phf2	Mm_Celera	13:48844006	CACACTCAAACACAA[-/AG]AGATCTTGAGAAAGG	18676
rs252792123	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48818142	TCTCCAGGCTCAGGA[G/T]GCTGCCTGGGTCTGG	18676
rs252853826	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48840165	TCCAAGACAGGTGGA[C/T]AGATCAACAACATGT	18676
rs252872235	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48864941	CACAGGCATTCAGCA[-/C]CGGCAGCCCTGTTGT	18676
rs252896868	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48849087	TATGCTCAGAGCCGA[A/G]GCTCCATCTCCTGTC	18676
rs252937344	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48843845	GCTCAGTGACTAAGA[C/T]ACCTGCTGCCAAACC	18676
rs252972771	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48819811	GACCTCCCGTCTCCT[-/C]CCATCTCATATGAAG	18676
rs253038293	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48850213	AGGGCTCTGCCCTGA[A/C]CAGGCCAAGATGTCA	18676
rs253050760	in-del	-/GGAGGC			cds-indel	Phf2	Mm_Celera	13:48804630	CGAGGTGGTACCCGT[-/GGAGGC]GGAGGCAGAGGTGGA	18676
rs253110212	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48833616	ATCTGGAGTCTCCTT[A/G]GAAATGACTCCGAGG	18676
rs253119862	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48837932	AGAAAAAGCACTGGG[C/T]AAAATTCCAACACCT	18676
rs253173309	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48839489	GTGTTCAAAAAATAA[A/G]GAGAAAGAGGAGGGG	18676
rs253178058	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48844568	ACATAGCCCATTCTG[G/T]CCTCAAACTCAGTAT	18676
rs253178150	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48837555	AACTCTTATTAATAG[C/T]ATATAAAAATCCTCA	18676
rs253223635	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48820653	ACTAGCTTCTACCTC[A/G]CTTCCGTGCTAGCTT	18676
rs253240972	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48831170	GTTACCCACGAGAAA[C/G]CAGGACCTGAAGGAA	18676
rs253283449	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48821721	CTCACTGGCAGAGCC[A/G]AAACACCGGGGATGT	18676
rs253298174	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48838442	CACATATATAAAACA[G/T]GCTAGCCCTAATAAA	18676
rs253341622	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48822439	AGCCTCATTCTCATG[C/T]TCCAGGACAGACGCG	18676
rs253377054	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48809178	CCAGGGGTTGGGTCT[C/T]GAGCAGCTTCCTGGT	18676
rs253401277	snp	C/G			intron-variant, upstream-variant-2KB	Phf2, LOC102642832	Mm_Celera	13:48869613	AGGAAGGTCAGGGAC[C/G]GTCCAGAACCACACA	18676
rs253418305	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48845404	ACACACAGAAGCAGC[C/T]AGCTGAGTCAGTAAC	18676
rs253578816	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48817194	GGGTGCTACCCCCAC[C/T]ACAGCACAAACCCTC	18676
rs253580652	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48809000	CCATGCCCTTTCTGC[A/T]CTTTCCTAGCAATGC	18676
rs253623277	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48826304	GTGCATGGCCGTACC[-/G]ACACCCCCAGGACAA	18676
rs253628867	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48836364	GGGGACCTAACGAGA[C/T]GGCTTAGTCAGTAAA	18676
rs253643958	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48809674	CAAACTACAACCAAA[C/T]ACCTGGAGCACTTCT	18676
rs253743794	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48835027	GCTCTCACTTAACAT[A/G]GGCTAGCCTGCCCAC	18676
rs253747533	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48863091	GACTCTTAAGACACT[-/A]AAAGCATGAACAAGA	18676
rs253822701	snp	C/T			synonymous-codon	Phf2	Mm_Celera	13:48816032	CTTCTCCAGCCTCTG[C/T]TCCTCCTCCATCTTC	18676
rs253836290	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48829616	GGCCATGTAAGCAAA[A/T]GGTAGCCTTTTCAAC	18676
rs253842829	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48857285	CAGGCCAGGCCCCAC[C/T]CCCGAACAGTCTGCA	18676
rs253843163	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48844810	CAAAGGCTAGAAACT[C/T]AAATTATATAAAGAA	18676
rs253891169	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48830416	GAGGAGGGGGAAGAG[A/G]AAGAGGAGGGGGAGG	18676
rs253891223	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48822537	CCAGAGCTGGTCTGG[A/G]GAAGTGTAGTTCGCA	18676
rs253896811	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48856007	TCATGCACACCATGG[C/T]AGCACCATGATACCC	18676
rs253947452	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48823436	GGTTGGCGCTCAGAA[A/G]AGATGCTTCTCAACG	18676
rs253967238	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48860399	ACCAAGCTCTCAGCC[A/G]GTACACTGGTGAAGC	18676
rs253995300	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48854101	TGATTGGCTGGAGCT[G/T]GGGACAGGCCGGAAG	18676
rs254004553	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48812178	TGTGGGCCATGGGAC[A/G]GCTGTCTAAGCTCCC	18676
rs254060115	snp	C/T			downstream-variant-500B	Phf2	Mm_Celera	13:48801658	CAAGGATGCACCTGG[C/T]CAGAGCCTGCTGGAG	18676
rs254070911	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48828645	TCCAGGTTTGGTTAT[A/G]GATCCTGTCTAAAGA	18676
rs254196564	in-del	-/CAG			intron-variant	Phf2	Mm_Celera	13:48831449	TTTCACAATAAACAT[-/CAG]CAGAAACCCACCAAC	18676
rs254230459	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48851419	CATAAACATTCTCTC[C/T]AGGTGGTGACCCACA	18676
rs254271021	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48811247	CTGCAAAGCACTCTC[C/T]CCAGACTTGGGGCAC	18676
rs254279883	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48862147	AACCAGGAACCAAAA[A/C]CTTTTCTTCCTTTAG	18676
rs254283765	in-del	-/AG			intron-variant	Phf2	Mm_Celera	13:48847109	CATTCGCTGGCAGGA[-/AG]AGAACACTTGAACAT	18676
rs254302696	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48818863	CTCAAGGTCCTCTGA[A/G]CCTCCCACTTGTTCT	18676
rs254347045	in-del	-/CGCTTTTTAGGGCCCGAAAA			intron-variant	Phf2	Mm_Celera	13:48835737	TGTCCCTCCCAAGAG[-/CGCTTTTTAGGGCCCGAAAA]CCTGCTCAGAAGCTT	18676
rs254366171	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48861788	GGGTTTGCCAGCCAG[C/T]CGGCCAGTCTTGCCA	18676
rs254367641	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48867953	AAACTGTTTGCCAGG[A/G]TAAGGAATCCAATGC	18676
rs254368682	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48848081	GATACATAGTACACA[-/G]GACATACATGAAAGC	18676
rs254374391	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48819649	GGGAAGGACACAATA[A/G]GTTAGTTAGTGTGGT	18676
rs254681619	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48834196	GGCCCCAATGTCCCC[A/G]GAATCTTGGATAAGA	18676
rs254709243	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48856648	CCAGTCTTAGCAAGA[A/G]AAAGGTGGAAATTGG	18676
rs254715118	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48851245	AGCGATAGACCCTGC[A/G]GCAGACACTCCCTCC	18676
rs254730556	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48839679	AAGTCTGCTTATAGA[A/C]TAAGAGAATGTTTTT	18676
rs254731481	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48833312	GCAGCCTCTGCTCAA[A/G]CCCCTCCCCCCCACC	18676
rs254786104	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48839363	CCTGAGGAACTCACT[A/G]ATGGTTACTGCTTAG	18676
rs254826917	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48854022	ACTACTGGAAGTTTT[A/T]GGGGACTAGAGCAGA	18676
rs254867147	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48830187	TACGGGCAAAACACT[C/T]GTACAAATAAAATAA	18676
rs254890124	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48864788	TCGCAGTACAACGGC[G/T]AGGGTCAGGAAAGCC	18676
rs254925704	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48841177	TCCGGTCCCTCCAAG[-/T]TTCATTACCTCGATC	18676
rs254984966	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48805459	TCTGGATGGGAAGTC[A/G]CACCACATCTGCTCT	18676
rs255071908	in-del	-/TGG			intron-variant	Phf2	Mm_Celera	13:48841104	TAAGAAACTCAGGGT[-/TGG]CAGCTGGTCCCCTCC	18676
rs255083813	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48839389	CTTAGGGAGGCAGTG[C/T]CAGTCTCTTCAGTAC	18676
rs255106582	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48816625	CTGGGGTTATGACAG[C/T]AGAGGAGACCAGGCA	18676
rs255144546	in-del	-/GC			intron-variant	Phf2	Mm_Celera	13:48845150	AGACTTGGCAGTAGA[-/GC]CTTCACCCACTGAGC	18676
rs255184443	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48847083	AACCATGGCACATCC[G/T]GGAAAGGAAACATTC	18676
rs255205964	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48867680	TCTAGTTATTGTGGG[A/G]TTTGTTTTTGTTTTG	18676
rs255236970	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48832724	AGACCTTGACCAAGA[A/C]CCACAGGCCAAAATC	18676
rs255260140	in-del	-/TTTTG			intron-variant	Phf2	Mm_Celera	13:48844337	CATTCATTAATTAAA[-/TTTTG]TTTTGTTTTGTTTTG	18676
rs255276320	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48818702	GGGAAGGACCCCTGA[A/T]CTATCCCAGCTTTGA	18676
rs255277896	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48866211	GGATAAAGGCTTCAA[C/T]GCCAGCTAGGCTACT	18676
rs255304833	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48829320	GGAAAAGAGAGCAAA[A/C]CCAAATCCTTCTACC	18676
rs255371291	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48830047	AGCTGCCTACAATTC[A/C]AGCGCCAGGGGAGGT	18676
rs255378397	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48823382	CCAATAAAGAGGGGT[A/G]AGAGAAAGGTCTCAG	18676
rs255442794	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48804272	GCCCCTGATGACCTG[A/G]GACCAGAATCCTCTT	18676
rs255448132	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48841794	TGAAAAGGCCAGGTC[A/C]GGGGTGGCTGTGTGT	18676
rs255504147	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48823525	CCAGAGACCCCCCCA[-/C]CCCCCTCACCCCAGT	18676
rs255511496	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48843444	GCAGAAAGACACAAC[C/T]GAATGCCACTCATCA	18676
rs255517215	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48805137	GCCACTCTCCTGCCT[A/G]GCAGGAGACACAGAG	18676
rs255540211	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48868558	CTGACAAGCTGTTCA[A/G]ACGTGAGGTAAAATG	18676
rs255602047	in-del	-/CC			intron-variant	Phf2	Mm_Celera	13:48834416	AGCCAGGGGACACGG[-/CC]TCTCAGCTTGCACTG	18676
rs255684226	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48869122	TAACCAGAGGTGCTA[C/T]AGGTCTTGGATTGAG	18676
rs255725571	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48823559	ATTTAGTTGCTATCA[A/C]ATCAGCCGCATCCCT	18676
rs255861096	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48857547	AGGAGGTGCAAGGCA[A/G]AAGCTCCAGCCCTGG	18676
rs256033870	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48849594	ATTCTTCTTCCAGGA[A/T]GGGGAGAGGGGTGTT	18676
rs256076972	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48844203	GTGCATGCGGTGGTC[A/G]GAGGGGCTTGCATAG	18676
rs256112213	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48828044	AGTCAGAGTATAAGC[C/G]TATCTAACCTGGAGC	18676
rs256130934	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48842417	GGAGGGGCGAGCATG[C/G]CCTTCCAGGATACTC	18676
rs256172105	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48806849	ATGGGAGCAGTGACA[-/C]CCCCCCCCCCGCCCC	18676
rs256178533	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48820419	CCCTCTTCCCCTCAA[C/T]ACACAGATGTCAGCA	18676
rs256249478	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48815136	ACTCGCTCCTGAGGT[C/T]CTCAGCACCCAAATC	18676
rs256283409	in-del	-/TG			intron-variant	Phf2	Mm_Celera	13:48830708	GAGCGAGCCACAGAC[-/TG]AGAGAACCCTGCTCC	18676
rs256308011	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48818493	GGGGGGTGGGATGGG[A/G]TGGGGGGAGGGGCAG	18676
rs256313084	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48806573	CAGTGGACAGCAGTA[A/G]ACCTCTGGCTATCAG	18676
rs256321118	in-del	-/AT			intron-variant	Phf2	Mm_Celera	13:48842132	CTGTAATTTACAGTC[-/AT]AGAAAAGTCCACCAC	18676
rs256331814	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48838294	CACTGCTGTCTTCTA[C/T]TCAACAGTGTTAGGG	18676
rs256334668	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48850047	ATATCACATAATCCA[C/T]ACGCAAAGCAAATAC	18676
rs256389294	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48844895	CACTTGGGAGGCAGA[A/G]GCAGGTGGATTTCTG	18676
rs256389821	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48811160	ACCGGGAGACTTTGG[A/G]AGAGGAACTGCCTGC	18676
rs256441325	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48857641	GGATATCCCTGACCG[G/T]AAATCCCATTAGGCC	18676
rs256444457	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48840501	ATTGAGTGTTCACAC[C/T]AGCCACAGAGTATTC	18676
rs256508284	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48818570	CAAGGCTCTCTGGGA[-/G]CCACCTCTGCTAGTG	18676
rs256516871	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48856415	ACTGAGTGCTGTGCA[A/C]ACAGCTTTTCTGCAA	18676
rs256625200	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48811577	ACATATATTCTCCTG[A/G]AAGTCAGGCATTCCC	18676
rs256648248	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48836252	AGCTGTATTTAGCAC[G/T]ACTTTTAAATTAAAT	18676
rs256709920	snp	A/G/T			intron-variant	Phf2	Mm_Celera	13:48835560	CAGCAAGCCTGCCTC[A/G/T]GTGAGAACCACTCCC	18676
rs256748550	snp	G/T			downstream-variant-500B	Phf2	Mm_Celera	13:48801505	CCCAGACAGGGCTGA[G/T]ACATCTTCAGCCTTG	18676
rs256778087	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48806127	GGCCTCACAGGCTGC[C/T]ACCCACCCCCACCCC	18676
rs256815057	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48844734	TTTGTGAGAACTAGC[C/T]ACCAGTGTACGTTAT	18676
rs256866927	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48824270	CACCTGACCAGGCTG[G/T]CTGGGGTAGCTCCGT	18676
rs256873871	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48855860	AGAAAGTGAGATGCA[C/G]AAGAAACTGAGTAGG	18676
rs256910300	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48851664	CAGGTGGAGTAGCTA[C/T]CCAGAACATTTTGGC	18676
rs256944032	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48810771	CTATCCTGTCCTCAA[C/T]CCAGGCCACAGGGAC	18676
rs256963715	in-del	-/GTGTGT			intron-variant	Phf2	Mm_Celera	13:48862880	GACAAATACATGATA[-/GTGTGT]GTGTGTGTGTGTGTG	18676
rs256976122	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48851036	TCCATAGGTAAAGTG[C/T]CTGTCAGGCAAATGT	18676
rs257087186	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48844485	CCTCTGACTCCCAAG[G/T]GCTGAGTGCTAAATT	18676
rs257213245	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48814796	AGTCTCAGGGACACT[C/T]CTACTGAAATGACAG	18676
rs257325967	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48806700	GAAATCAGGTACCTG[C/T]GTCAGGCAGGCCCTG	18676
rs257343383	in-del	-/AAA			intron-variant	Phf2	Mm_Celera	13:48856571	GGCAGAAGGGCCAGG[-/AAA]AAAAAAAAAATTCAA	18676
rs257353973	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48819769	GGGGTGCCCACCCAC[C/T]CAGCACCTGCCCTAC	18676
rs257370835	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48834842	GGGTAGGAAGAAGCA[C/T]TGGATTCACAACAGC	18676
rs257439599	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48834237	TGAACAGGAGTGTGG[A/G]CACTCCCACTGCCAA	18676
rs257500579	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48862027	CATGGCCTCTGGCCA[C/T]CACATTCACCCCTGC	18676
rs257540134	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48812626	ACGAGTGTGGCCAAC[C/T]GGAGCGAGCAGGGTT	18676
rs257571739	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48861166	TCAAGAGAGCAATGT[A/G]TAACCTATAGACATT	18676
rs257579197	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48864041	ACATGGCACTGTGTG[A/G]GTGAGCCTTAAAAAT	18676
rs257592086	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48826247	CTATGGCCTCCCTGG[A/G]GGACATGGTGGGGTG	18676
rs257633016	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48812026	ACCCTGGACGGGCCC[A/G]TGGAGTTCTTCCCAA	18676
rs257658350	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48826960	CCCTTTCTGTGTCTG[A/G]TCGGGAAAAGTTGAG	18676
rs257680848	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48836563	GCCCTGTCTCAAAAA[A/C]CAATTACAGCTCCTA	18676
rs257716946	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48815853	TACAGGGCAGTGCAC[A/G]GCATTTGCCATGTAT	18676
rs257770706	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48842247	ATCAGCTTTAAAGGC[A/G]GAAAGACTTATTTTG	18676
rs257785641	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48816402	CTGGGGACAGGCAGA[C/T]GCGCCCTGGCACAGG	18676
rs257788377	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48828469	AGAGAGCCCCACCTC[C/T]ACTCCTGCCCCCGCC	18676
rs257795492	in-del	-/AAAAAA			intron-variant	Phf2	Mm_Celera	13:48838116	CTCCTGACTCTTCAG[-/AAAAAA]AAAAAAAAAAAAAAA	18676
rs257861285	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48813141	TCACGGGGAGACTAG[-/T]TTTAAAGAGTTCTAT	18676
rs257916686	in-del	-/TA			intron-variant	Phf2	Mm_Celera	13:48820401	CCAGAGCATGGAACC[-/TA]CCCCTCTTCCCCTCA	18676
rs257922404	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48864706	CAAACCTTAAGCCAA[G/T]TGTACATGCAAGGTA	18676
rs257934665	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48857905	TTAAACTTATATGTG[C/T]CTGTCTCTCTGTGTG	18676
rs257999174	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48856642	AGAGACCCAGTCTTA[G/T]CAAGAGAAAGGTGGA	18676
rs258008714	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48822926	ACCCTGAGGACAAGG[A/G]TGTGTCTAGGGGTGT	18676
rs258082818	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48823741	TTGACTAGTCGGCAG[A/C]CTGACTCAGTTTCCC	18676
rs258093060	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48816377	GCTCACACAGACTTT[C/G]CTCGCAGCTCTGGGG	18676
rs258095323	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48834274	CCTGTTAACTGGACA[A/G]CCCTGGTACTGGAGT	18676
rs258110439	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48809833	AGAGATCTCCCTCCA[A/G]CACAGTATCCTCGCC	18676
rs258133403	in-del	-/CT			intron-variant	Phf2	Mm_Celera	13:48858613	TTGCTCTCCCTGAGC[-/CT]CTCTACCATTCAACC	18676
rs258175464	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48839295	TCTAAGACTGGGTCA[A/G]GCAACAACAGGTCGT	18676
rs258178195	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48839886	AGTGCAAGTCAGACC[C/T]CTCACTCACTCAGCG	18676
rs258191364	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48825325	TGGGTGTGTGTGAAC[C/G]ATAAGACAGGCATCC	18676
rs258238261	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48846687	TGATGGCCGTTACAG[A/G]ACACAAGCATGTGAC	18676
rs258314923	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48859691	TCTCCACCAGGGCTA[C/T]CCATCCTGCACTCCA	18676
rs258506030	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48837868	TTCCTCAGACGTTCT[C/T]ACCTTAGATAAACGC	18676
rs258548099	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48814103	GCCAGCAGACCATAG[A/G]CCCTCACAGGCAAGA	18676
rs258564628	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48807927	GGCCCTTGGCTCACA[A/G]CCAGGACACTTGGAC	18676
rs258586450	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48833011	TGCCCCAGATCCATA[A/G]AGGAGAGTCAGGAAA	18676
rs258605313	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48804797	GCACAGACAGCTCTG[C/T]CCCAACCCAGATGCA	18676
rs258615601	in-del	-/TTGGTTGT			upstream-variant-2KB, nc-transcript-variant	Phf2, LOC102642832	Mm_Celera	13:48871817	TTGTTGGTTGGTTGG[-/TTGGTTGT]TTGGTTGGTTGGTGA	18676
rs258645693	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48831504	TCCTTCTAACGTAAG[A/G]GAGAAATAAAGATTT	18676
rs258707175	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48841648	AGACCTGTGTGTGGT[A/G]TGTATACACGTAAGT	18676
rs258777007	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48831831	CACAGCAGGTTCCTG[C/G]TTTTTGCTCTCCTGG	18676
rs258794484	in-del	-/GCGC			intron-variant	Phf2	Mm_Celera	13:48806335	GCTCAGGACTCCCCA[-/GCGC]GCGACTCCTACACTG	18676
rs258830644	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48828518	AGTCAAGGAGATGGA[A/G]CCTTGGGTAAAGCAC	18676
rs258834783	in-del	-/GTGTGTGTGTAT			intron-variant	Phf2	Mm_Celera	13:48827680	TTATCATGTAAATAG[-/GTGTGTGTGTAT]GTGTGTGTGTGTGTA	18676
rs258890575	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48821007	ACTCCAGAAAAGCCA[C/T]AGTGCCTCCCTCCCA	18676
rs258917200	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48835733	CAGTGTGTCCCTCCC[A/G]AGAGCCTGCTCAGAA	18676
rs259018898	snp	C/T			synonymous-codon	Phf2	GRCm38.p3	13:48804516	CTCAGGTGAGCTGCC[C/T]TCCTGTGAGGCCTGG	18676
rs259035020	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48835927	TCTTGGTTACAGGTG[A/G]CAAAGAGAGGCCAGT	18676
rs259062349	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48864248	GAGAGGAACACATAA[C/T]ACACATGCATCGAGT	18676
rs259089293	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48831427	TAAGCTCAGCTGCCC[A/G]TGTGAGCTTTCACAA	18676
rs259135430	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48846912	ACATACCCTGACTGT[A/G]TGATTCCACACATGC	18676
rs259145424	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48838765	CTGGTACCTAGCTAG[C/T]TAGAAACAGACCAGC	18676
rs259208640	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48827945	TTTTTATGTGGGTCC[C/T]AGGGATGCAAGGTCA	18676
rs259218868	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48827930	CACTAACACATTAGC[-/T]TTTTATGTGGGTCCT	18676
rs259233494	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48845650	CACACCCTGAACATT[C/T]CATACAGTCCACAAA	18676
rs259280212	snp	C/T			upstream-variant-2KB, nc-transcript-variant	Phf2, LOC102642832	Mm_Celera	13:48871640	CAGGACCCCTTATTA[C/T]AACCCATAGACCCAC	18676
rs259282314	in-del	-/TG			intron-variant	Phf2	Mm_Celera	13:48842708	GTGTGCACATGTTCA[-/TG]TGTGTGTGTGCATAC	18676
rs259505037	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48815417	CAAGGACGTTCCACA[C/T]AACACAGTGGTGGTG	18676
rs259518480	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48836982	AAAGCCCAGGGACTG[A/G]TTCCCGCCACCCAGC	18676
rs259564147	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48807256	GACAAACTGTGGATG[A/G]GGACAAAGTTTCCTT	18676
rs259582344	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48842781	AGATCAACATTGGAC[A/G]TCTTCCTTGGCTGCT	18676
rs259634689	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48847236	CAGTTCCCAGGGTTT[-/G]GGGTCAAGTGAAAGG	18676
rs259643357	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48842164	GTAGGAAATGCCCAC[C/T]GAACTGGCAGCTAAC	18676
rs259681876	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48861214	CCAGCTGCCTCTTTT[C/T]CTTTTTCCTTGTTTT	18676
rs259706905	in-del	-/AC			intron-variant	Phf2	Mm_Celera	13:48867089	TACCAAATGGACCAG[-/AC]ATGATACCTGAGGGC	18676
rs259717140	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48811710	AACTCTCACTCTATC[A/G]TGCCAGGCTAAGCCA	18676
rs259834928	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48866986	TACAGACACAAGGAA[A/G]GACTATGGTTTTTAA	18676
rs259840498	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48867349	ATCCCCACTCCCCAC[C/T]GCCCTCTCCAAGAAA	18676
rs259980873	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48813191	TAGTCTCAGGTTCAC[A/G]CTATGGGTGAGGTCC	18676
rs260020797	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48803733	AAAGACCAAGAGTGA[C/T]AGCGACAGGAGGAGA	18676
rs260049265	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48823804	GCACCTATTGGAAGC[A/G]TTCAAAGGTACCTTT	18676
rs260094367	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48857952	CAGATGCCCATGGAT[C/T]CCAGAAGATGGTGTT	18676
rs260134412	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48806983	AGCCCAGGAACGAGA[A/G]CAGGTCCCTAGAGGA	18676
rs260166717	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48822005	AGAGTCTACTGGGTG[A/C]TAGGGACTCTTGGAC	18676
rs260172908	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48827203	GACTGTAGGTGTCCT[C/T]AAAGATGGAGGAGCA	18676
rs260185458	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48851133	CAGTTCTGGGAAGCG[A/G]AGAGAGGCAGGCCCT	18676
rs260186757	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48862853	AACATATACACATGC[A/G]CACATACACACTGAC	18676
rs260233821	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48844153	AGATCAGGGAACATA[C/T]GGAATCCTGAGCCCA	18676
rs260234653	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48811516	GAGATCCAGGGTACT[A/G]AGGATCTCTGAGACT	18676
rs260253343	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48819946	TCTTCTTATGCCTGT[G/T]CCCTAAGGGGTCATG	18676
rs260294065	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48855160	TAGAGATGCCAAGGC[C/T]GTGGGAGGTGAGGGG	18676
rs260296090	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48843193	TCCAATCTCCTTTTA[A/G]CATATTTTTTGTTTG	18676
rs260322858	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48829471	CAAGACTTACAGATC[C/T]TGACTTCAAAATTTA	18676
rs260345106	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48848343	CTATAACTTGTCTAC[A/T]AAAATGCTGAGCTTG	18676
rs260406935	in-del	-/TT			intron-variant	Phf2	Mm_Celera	13:48838860	GTGTGGGGGGGTGTG[-/TT]TGTGTGATATACTGT	18676
rs260454643	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48809497	TCAGATGAGCCCCGC[A/C]TAGAAAAGAAAACAC	18676
rs260499917	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48818267	CATCTCCCTAGCAGG[C/T]TCCCTTGGTCCTAGG	18676
rs260525519	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48834131	CAGAGAGCCCAGGAG[C/T]CAGGAGCACCCACCC	18676
rs260566845	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48837245	GTGCACACACTCGCA[C/T]ATACATACACACAGA	18676
rs260570432	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48839648	TTGTACAACAGAGAA[C/T]GCCGTTAAGAAAGAA	18676
rs260572564	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48840371	TGGTGGGAAAAGGGG[A/G]GATGTGGGTTTGCAG	18676
rs260597128	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48825739	ATCTGAGCTGTTCAG[G/T]GTGCTTTAAGAGAAA	18676
rs260622314	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48839888	TGCAAGTCAGACCCC[G/T]CACTCACTCAGCGGG	18676
rs260623491	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48849518	CCAGAGTATTTGCTG[C/T]CTGCCTGCTTCTGAA	18676
rs260647753	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48818180	AGGCTCAGACTCCAA[A/G]CCTGGACCTGAGGTT	18676
rs260671130	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48854434	CAATAAGGCCCACAG[A/G]CTATAGGGCACTCCT	18676
rs260716857	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48830490	TCCTCTGGCCTCCCA[A/G]TGCAGGTGCGCACAT	18676
rs260718453	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48865300	GCCAAAAAGTTACAG[C/T]TTGAAAACAAAAACA	18676
rs260781403	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48817472	ACAGGGGCTCCAGTG[C/G]CCCAGCATATGAGGG	18676
rs260781555	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48826018	ACATTGGCTTTGAGT[C/T]GAACCTGCCAACCAA	18676
rs260804413	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48806195	GGAGGCTGCTGCTGC[A/T]GCAGCGAGTGAGAGA	18676
rs260919208	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48829103	CACCCTGGAAGCAAG[A/G]CACACAGGTCCACTG	18676
rs260937661	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48836627	TCAGGCAAGAAAAGG[A/G]AGGGCCTTTTCTTGA	18676
rs260977854	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48867582	AGCATGGGTGACTTA[A/G]GAGATCCTCATTCTA	18676
rs261001844	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48834673	GAGCATATGCACAAG[-/T]CCCGTCCCTGTGTTC	18676
rs261059001	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48831243	GATTTCTTTGGGGGG[C/G]GGGGTAGGGTTAAAG	18676
rs261097980	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48814462	GGGCTATTAGATACT[A/G]TGTATCTTTCTTCTT	18676
rs261098888	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48846504	TGCTCTGAAAAGGCT[A/G]TTGTTTTGAGAATTA	18676
rs261104359	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48844342	ATTAATTAAATTTTG[-/T]TTTGTTTTGTTTTGT	18676
rs261115251	in-del	-/GGGCAGAGGGAGCAA			upstream-variant-2KB, cds-indel	Phf2, LOC102642832	Mm_Celera	13:48872533	GCCTACCAAAGGTGG[-/GGGCAGAGGGAGCAA]GGGAAGAGGACACCC	18676
rs261137761	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48824154	CTGCAGCCCCCATGC[A/C]GCAACAGAGAACCAG	18676
rs261178125	in-del	-/ACAG			intron-variant	Phf2	Mm_Celera	13:48849883	CACTGCCAGACACAA[-/ACAG]ACAGACAGACAGACA	18676
rs261239772	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48834152	GCACCCACCCCACGT[-/A]AGTACCAGCCTCACC	18676
rs261387091	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48823818	CATTCAAAGGTACCT[G/T]TCACTCCAGGTTGGG	18676
rs261432595	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48845948	CCCATAATCCCAACA[C/T]TGGGTGGTAGAGACA	18676
rs261481741	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48857960	CATGGATTCCAGAAG[A/G]TGGTGTTGGATGTCC	18676
rs261535773	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48851602	CTGGAGGAAAGTGAG[C/T]CTATTGACATGGCTT	18676
rs261590506	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48855370	AGACAAGGAACAATC[C/T]CAAAACCAGGCTACT	18676
rs261591976	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48833719	AGATGAGCACACACC[-/A]CTTTACCCCCATCCT	18676
rs261624784	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48865617	AGTTCCAGGGAATAT[A/G]AAACCCTATTCTGAC	18676
rs261633657	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48849196	ATCCAGGTAAGCACT[C/G]TAATTTATAGAAACT	18676
rs261634342	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48830978	GTGACACACATCAGA[A/G]GGATACACACAGCAA	18676
rs261662209	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48827312	AGGACACAGTGAGCC[C/T]CTGGATGCCACAGCT	18676
rs261667014	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48860588	GAGGGGAAAGGATAC[A/G]AGGAAGGAGGTGGAG	18676
rs261799344	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48845974	GACAGGAAGATCTCT[-/G]GGGCTTGCCGACCAG	18676
rs261802136	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48833318	TCTGCTCAAGCCCCT[-/C]CCCCCCACCAGGCCC	18676
rs261821578	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48845247	CAACAGTGTATACTG[C/T]GCCTGATGATTATGG	18676
rs261935937	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48841080	TGATGACAGTGCTCT[A/G]AGTCCTCTCTAAGAA	18676
rs262001231	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48826928	AATTGGCAACTACTC[A/G]GGAAATATTTATTTT	18676
rs262033846	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48818932	GTCCGCTCTGAAGAG[C/T]GAGAGCCATAGTAGG	18676
rs262038661	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48848082	GATACATAGTACACA[A/G]ACATACATGAAAGCA	18676
rs262067317	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48859970	CTATCCTCAACTGAG[C/T]CTTTAACCTTAAAGA	18676
rs262099322	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48823451	GAGATGCTTCTCAAC[-/G]GTGCCTTGTGTGCCA	18676
rs262143888	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48854958	TAAATGTGTGTGTGT[A/G]ATTTCTAATCAGAGG	18676
rs262144369	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48842525	ACCAAGCATCCAGCA[-/C]ACAGGGCTTTAGGGC	18676
rs262159424	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48825462	GTGCACTGAGTGTAA[A/G]TGGGTGTGTGGAAAC	18676
rs262166312	in-del	-/ACATAAACAT			intron-variant	Phf2	Mm_Celera	13:48862056	CACATGTGTGCACAC[-/ACATAAACAT]ACATAAACATACATA	18676
rs262192001	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48822830	TCCTTGGCTTCCTGT[C/T]CCACAACTGGCCATC	18676
rs262213675	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48821814	GTGTGGCGGGTAGAG[C/T]CTACTGGGTGTTGAG	18676
rs262223638	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48815167	TACACATCCCTCCCC[A/T]TGGCATCCATCAGTT	18676
rs262283629	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48811404	AACTGGGCACCAAGG[C/T]GAGGGCCTAGGCTCT	18676
rs262501649	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48843093	TAAATACCTTACTAC[A/T]GAGTTACACCTTTTG	18676
rs262532995	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48820760	AGGTGGAGGAGGGAG[C/T]GTGTCTGAGGTCACA	18676
rs262534167	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48853507	TCTTCTAGATAAAGG[A/G]CAGGGTCTCTTTAAA	18676
rs262564932	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48813248	CTTTCCTAGGGTCCT[C/T]AAAACCACGAAGGTT	18676
rs262595308	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48810497	ACATTTCCTGAACCC[A/G]AGGAGAGGGAAGCCA	18676
rs262598455	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48839608	AAAGAGGGAGGAAAA[A/T]TTTCAATTTAATTAA	18676
rs262620405	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48816880	AGCCATGAGGATGGC[C/T]CCCAAAATGTGGGAG	18676
rs262634432	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48847624	ATGTGAACATACACA[A/T]ATACACATACACCAC	18676
rs262704200	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48816626	TGGGGTTATGACAGC[A/G]GAGGAGACCAGGCAC	18676
rs262752869	in-del	-/AAAT			intron-variant	Phf2	Mm_Celera	13:48827626	GTCTCAAAAAACTTC[-/AAAT]AAATAAATAAATAAA	18676
rs262768223	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48847128	AACACTTGAACATAC[A/G]CCGAAAAGTGAAAGC	18676
rs262803996	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48838376	GAAAGAGGTGATGTG[A/C]TCTTTATTTGCAGAT	18676
rs262807177	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48813094	CAGGGACAGAGCAGC[A/T]GGTCAGGGCAGGGCA	18676
rs262812307	in-del	-/GGG			intron-variant	Phf2	Mm_Celera	13:48831236	TGGCAGGATTTCTTT[-/GGG]GGGGGGGGGGGTAGG	18676
rs262831944	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48844939	CCTAGTCTACAGAGT[A/G]AGTTCCAGGACAGCC	18676
rs262862753	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48836778	CACACATGGAAGTAA[A/C]GACACTGCCACTGGC	18676
rs262897120	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48842503	TCCCATCTACACTAT[A/G]GGCTGGACCAAGCAT	18676
rs262919044	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48824207	AGGCCAAACAGGCCT[-/C]TCATGCCTCTACACT	18676
rs262972694	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48840832	CACTCACAGGAGCCA[C/T]GAAGCATTCGTACGG	18676
rs263161468	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48839072	TTCCTAATGCCCACC[A/G]GACACCCTATGGAAA	18676
rs263173361	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48836314	CCTTATGATATACTG[C/T]ATGATAAACTTCATA	18676
rs263241203	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48823281	GCATCTCACTTCCTA[-/G]GGGAGGAAAGGAAAG	18676
rs263266554	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48812314	GGTGGGGGGAGAGGG[A/G]GGTCCAGGCTGTGCC	18676
rs263274542	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48840307	CAACTCACAGATGAA[A/G]AGTCTATAACAAGTA	18676
rs263275584	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48822588	TGTTGTTAAACACAT[-/C]CAGTTCTCTTAGCTC	18676
rs263336370	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48839380	GGTTACTGCTTAGGG[-/A]AGGCAGTGTCAGTCT	18676
rs263351785	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48832406	CCCATAATGGTGAGT[C/T]GACCCACAGTATAGG	18676
rs263393766	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48845732	ACCACAGCAACCATT[-/A]AAAATGCTTATTTTG	18676
rs263425181	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48808132	CCAGGGAGGGAATGA[A/G]GCCTTGGGTGGAATA	18676
rs263450720	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48808599	CTACAACCCATCCAC[A/G]CCTACACCCCTATCT	18676
rs263494693	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48830062	CAGCGCCAGGGGAGG[C/T]AATGGCCTTTTCTGT	18676
rs263535149	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48868229	GAGCTCATGCTATGG[G/T]GTACATGGGTAGGTT	18676
rs263559133	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48867794	TGGAACTCAGAGATC[C/T]ACCTGCTTTCATCTT	18676
rs263567448	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48815096	GCCATGCTGAGGCTC[A/C]CGTGGCTCCTAAGCT	18676
rs263623062	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48864775	TGCCTGCCCTGGCTC[A/G]CAGTACAACGGCTAG	18676
rs263634862	snp	A/G			downstream-variant-500B	Phf2	Mm_Celera	13:48801460	AGGGACACTTCTTGT[A/G]GTTGTCCATAGGGTG	18676
rs263680498	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48826782	AATGACTATGGACTG[G/T]TGGCTCTAGAATCAT	18676
rs263738837	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48861625	CCAGGACAGCTGGGG[C/T]TGGGGAGATGGCCCC	18676
rs263760533	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48837745	GTGCCCCCTGGAGGT[A/T]ACAGGGGAGCAGGGA	18676
rs263788936	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48814352	CAGACTGCCAGAGTT[G/T]AAATCAAGTCTCAGG	18676
rs263814426	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48859377	ATGAGTATCTCCCAC[C/T]TGCCCTGCATGCTTG	18676
rs263818771	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48805221	TGCACGAACCCTTCC[G/T]TCTCCTCACCTGCTG	18676
rs263858500	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48861034	CTGCCCTCAAAATAT[C/T]TAAAAACAAACTGAG	18676
rs263917973	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48834665	ACACACACGAGCATA[C/T]GCACAAGTCCCGTCC	18676
rs263934280	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48810347	CTAGGAAAGCTACTG[A/C]TCAGAAAATGAGGGT	18676
rs263943798	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48809849	CACAGTATCCTCGCC[A/G]GCACAGTACCCACTC	18676
rs264024513	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48855677	AAAGACAGCTACTGC[C/T]CATCCCCTGCCCAAG	18676
rs264050276	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48831934	GAAGGAGGATGCAGG[A/G]CTTCAGTGGATGGGC	18676
rs264057976	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48829846	GGTTTTAGATTGCAA[C/T]AAGAGCACAAGAAAC	18676
rs264082316	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48838914	ACGCATGTGTATACA[A/T]GTATGTTGATGCCAG	18676
rs264094337	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48853019	ATGACTCTAGCTGTG[C/T]TCTCCCTTATATCTA	18676
rs264123617	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48805052	AGGGCATCCTGGGTA[C/T]CATGTGAGGGAGAGG	18676
rs264145384	in-del	-/TGGGTGTGTGTGTGTGTGTGTGTGTGTG			intron-variant	Phf2	Mm_Celera	13:48842639	ACGGGTGGGGACAGC[-/TGGGTGTGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT	18676
rs264281284	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48822122	CCATCACAACCTGCT[G/T]GGACCAGTGGTGGGT	18676
rs264293337	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48836133	GGCTCCACCCAGAAA[A/G]GATGAAGGGAAGTGG	18676
rs264354343	snp	C/G			intron-variant	Phf2	Mm_Celera	13:48864615	GGGGGACACGCACTG[C/G]CTGTGGACCTCTTGT	18676
rs264431296	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48828455	AGCTAGAACTACTTA[A/G]AGAGCCCCACCTCCA	18676
rs264508399	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48804132	CCTGAGCTGAGAATC[A/G]GTCCTGTAATCAGTG	18676
rs264518921	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48835449	GGTGGGAGGGGAGAC[A/G]GGGCTGTAGAGCTGT	18676
rs264543952	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48851856	CAGTCACTGGCATGT[A/G]TGAGTACCCAGGAAC	18676
rs264557804	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48831473	CACCAACTGAGAACT[C/T]TGCCCAGTGATGCTA	18676
rs264574786	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48863682	CAACTCCACACCCAC[A/T]CCCCGTGAGGATGGT	18676
rs264579325	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48827641	CAAATAAATAAATAA[A/T]TCTGGAGATAAAACC	18676
rs264590760	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48847002	ACTGACACTAGTCTA[A/G]TGTCATAAACGCTAG	18676
rs264624809	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48858584	CTGGGTGATCTCTCT[A/G]CTACTGGGGCATTAT	18676
rs264627870	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48824481	TGCAACTTTCCTGAC[C/T]CCCACATCTGGTGTG	18676
rs264658993	in-del	-/GG			intron-variant	Phf2	Mm_Celera	13:48831237	TGGCAGGATTTCTTT[-/GG]GGGGGGGGGTAGGGT	18676
rs264710841	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48806803	CGCAGGATCATCCGT[-/G]GGGGCTTGGTTTTTC	18676
rs264715686	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48805507	ACTGGAGTATCTGTG[C/T]GGCGGTATGGGAGGT	18676
rs264786985	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48849561	ATTTGATCCACAAGA[A/C]AACATGCAGGGTGCC	18676
rs264803658	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48861082	CACCACAGAACATGG[C/T]AAATGACTGAAGAAG	18676
rs264806223	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48827690	AATAGGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT	18676
rs264875076	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48826223	GGACATGAACATGCC[A/G]GGAAAGCGCTATGGC	18676
rs264891545	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48818484	GGCCACCCCGGGGGG[G/T]GGGATGGGATGGGGG	18676
rs264995807	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48823717	TAGACAGGCCTGGAG[A/G]GCATCTTCTTGACTA	18676
rs265012726	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48815745	GTGTGTGTGTTGCCA[C/T]GTATGATGTCACATA	18676
rs265015861	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48844112	CAAGCATCGAGAGTA[C/T]GTGGCAAACTATTTA	18676
rs265082164	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48814278	ACACAGTCACGCACT[A/G]TAGAGAAAGATCTGA	18676
rs265113176	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48820309	GTTGGCTGTAGTTAC[-/T]TAGAGAGGCTGGCCA	18676
rs265138124	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48819982	GGCTCCTAAAGGGCT[A/G]TAATATCCCTTAGAC	18676
rs265171800	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48852016	CTCTGGGAGCCACAG[A/C]AGAGCCGTCTCTGGG	18676
rs265245907	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48839770	AATAAAACCATCTAG[A/G]TTTTAAATGAGCGAA	18676
rs265262124	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48817417	TAACACAGGAGAGCA[A/G]AGAGGTGTTATCCCA	18676
rs265262723	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48848211	TTCATCAAACGGCTC[A/G]CATACACCACACAGG	18676
rs265278924	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48809772	GGCAAGCTCAGGACC[A/G]GAATCACGGTGATGA	18676
rs265299927	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48845487	CTTGGTGTACGGTGG[C/T]TCCAGAGGGACAGTC	18676
rs265394168	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48838858	GTGTGTGGGGGGGTG[C/T]GTTTGTGTGATATAC	18676
rs265411541	snp	A/C			intron-variant	Phf2	Mm_Celera	13:48835688	ACCCGGAGCTGTTCT[A/C]CAACCACTTGCCCTG	18676
rs265428222	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48841152	GCCCCTCCCAGGGGA[A/T]GGGAGAAGCCTCCGG	18676
rs265533617	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48811673	AGAAGCCACAGCCAG[G/T]CTTCCCCCATGTGTT	18676
rs265600171	snp	C/T			missense	Phf2	Mm_Celera	13:48815997	AAGGAAAACTTGTCC[C/T]TGTTCCCAGCCAGGG	18676
rs265654179	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48808908	CAGCTTAGCCAGGTT[C/T]CCCTCTCTGGGTCCC	18676
rs265659819	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48838226	GCTAATATTACACAG[A/G]ATGATGAAAAGCCAA	18676
rs265690707	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48869086	CCCCTTCTCTGCCTC[A/G]GCAGCAGCCCAGCTG	18676
rs265693500	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48830690	GAAGCACCACACTAA[G/T]GAGAGCGAGCCACAG	18676
rs265723576	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48806477	ATTCCAGCTGTCTAT[C/T]TAAGCAGAGCACACT	18676
rs265724947	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48865532	GAAGTTAAGAACACA[G/T]GTTGCTCTTGCAGAG	18676
rs265777897	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48813492	CCAGCTGATGGGGAG[C/T]CACCCCCTGCTATTC	18676
rs265830996	in-del	-/ACAT			intron-variant	Phf2	Mm_Celera	13:48839152	AGGTATTAGAAGAAA[-/ACAT]GCATGAATGAACTCC	18676
rs265846683	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48859881	TGGGCAGCCGTTCTC[C/T]GTGTCCTGCCCCTGT	18676
rs265861297	in-del	-/CA			intron-variant	Phf2	Mm_Celera	13:48822034	ACAGGGGATACAGCC[-/CA]CTAGGAGCTGGGGCA	18676
rs265886547	snp	G/T			intron-variant	Phf2	Mm_Celera	13:48834864	CACAACAGCAGGCAC[G/T]GTGGAAAAACCAGGC	18676
rs265900486	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48810619	TGTTGGAGCCTCCCT[C/T]GTTAGCCTGCCCTGC	18676
rs265939257	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48839335	GGGCGGGGCTCATAA[A/G]GCCCCACCCCTTCCT	18676
rs266019342	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48845896	ATCTCAGTCTAACCC[-/A]CAGCACCCATAGAAA	18676
rs266028791	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48833099	GCCATAGACGCTAGC[A/G]TGCACTTGATTTTGG	18676
rs266063267	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48836426	TCAGATTCCCAGAAC[A/G]GATACAAGACGGTGG	18676
rs266094327	snp	C/T			intron-variant	Phf2	Mm_Celera	13:48864858	GAATGGAGTTGACAT[C/T]GTGACCTAGCAGACT	18676
rs266136676	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48828597	AGTGTGTGGCCATTC[A/G]TGCTGGAACAGCCAC	18676
rs266167558	snp	C/T			downstream-variant-500B	Phf2	Mm_Celera	13:48801687	AGTCAGCTGGCCCCA[C/T]TGTCACGTGCCCCAC	18676
rs266209703	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48826996	TCAAATAGCTAAGGA[A/T]AGAAAAGTCTTTACA	18676
rs266243318	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48862129	CACATCATAAAACTC[A/G]AAAACCAGGAACCAA	18676
rs386837070	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48823452	AGATGCTTCTCAACG[-/G]TGCCTTGTGTGCCAT	18676
rs386843110	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48855183	TGAGGGGAATCCAGA[-/A]CAGACTGGGGGCTTC	18676
rs386874561	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48831945	AGGGCTTCAGTGGAT[-/T]GGGCCCATGCCTTGG	18676
rs386884626	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48864014	TAAAAAAAAAAATCA[A/G]TAAACACCAACACAT	18676
rs386915208	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48848082	ATACATAGTACACAG[-/G]ACATACATGAAAGCA	18676
rs386948661	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48839347	TAAAGCCCCACCCCT[C/T]CCTGAGGAACTCACT	18676
rs386958704	in-del	-/ACCCTGGGAGTCCTTCATTC			intron-variant	Phf2	Mm_Celera	13:48858644	AGGCTGTCATCCCTC[-/ACCCTGGGAGTCCTTCATTC]CTCGATCCAGGAAAT	18676
rs386974391	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48813131	AGCAGGTCCCTTCAC[A/G]GGGAGACTAGTTTAA	18676
rs386992355	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48816661	CTGTCCACACACAGC[-/T]AATCAATCCATTCCC	18676
rs386996545	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48862618	CAGGAATAAAAAAAA[-/A]CAATAGGAATTTTTA	18676
rs387002604	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48826312	CCGTACCACACCCCC[-/C]AGGACAAATAGGGGC	18676
rs387031886	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48844176	GAGCCCAGCATTTTT[-/T]AAGCTTTGCATGTGC	18676
rs387051054	in-del	-/AGA			intron-variant	Phf2	Mm_Celera	13:48813599	AGGGACTGAGCAAGA[-/AGA]CCATGTCCCTCTTGT	18676
rs387052333	in-del	-/TTTGGTTG			upstream-variant-2KB, nc-transcript-variant	Phf2, LOC102642832	Mm_Celera	13:48871824	TTGGTTGGTTGGTTG[-/TTTGGTTG]GTTGGTGAGATATGA	18676
rs387054837	in-del	-/GA			utr-variant-3-prime	Phf2	Mm_Celera	13:48801947	AGAGAGAGAGAGAGA[-/GA]ACAGCTTGATGCCCG	18676
rs387073368	in-del	-/GGTC			intron-variant	Phf2	Mm_Celera	13:48845861	GAATGGAGCTTAGTC[-/GGTC]ACGTGTCACACGATG	18676
rs387079556	in-del	-/CTC			intron-variant	Phf2	Mm_Celera	13:48839167	AGCATGAATGAACTC[-/CTC]AAGCCTTTGGATTTG	18676
rs387097277	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48822682	GAGTGGTTTCTGGGA[-/A]GTCTTCCCAGCACCT	18676
rs387160378	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48823530	GACCCCCCCACCCCC[-/C]TCACCCCAGTCACAT	18676
rs387163594	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48848119	AATACACATAAAATT[-/T]AAAAAAAAAATTTAA	18676
rs387173565	in-del	-/TACC			intron-variant	Phf2	Mm_Celera	13:48820401	CCAGAGCATGGAACC[-/TACC]CCTCTTCCCCTCAAT	18676
rs387181670	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48847781	TACACACATATATAC[C/T]ACAAACATACACAAA	18676
rs387206010	in-del	-/G			intron-variant	Phf2	Mm_Celera	13:48847239	TTCCCAGGGTTTGGG[-/G]TCAAGTGAAAGGGGG	18676
rs387215048	snp	A/G			intron-variant	Phf2	Mm_Celera	13:48861889	AGGAAGGAAGGAAGG[A/G]AGGGAGGGAGGGAGG	18676
rs387239576	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48852504	GCTGACTTCCTTGCC[C/T]TCTCTCCCTCTCTCT	18676
rs387286435	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48858742	GCCTGTGCAGATGCT[-/T]GTGTGCAGCTGTGGG	18676
rs387304919	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48810046	CCTTCCAGCAGTATC[C/T]TTTCCAGCACAGTAC	18676
rs387347363	in-del	-/TCT			intron-variant	Phf2	Mm_Celera	13:48833592	CAGTTTCTACCTTCT[-/TCT]CTGAGAATCTGGAGT	18676
rs387357969	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48815672	GTGTGTAATGGTGTA[-/A]TGGGGGATGCATGTC	18676
rs387361924	in-del	-/TGTG			intron-variant	Phf2	Mm_Celera	13:48862896	GTGTGTGTGTGTGTG[-/TGTG]CTCGACACACACACA	18676
rs387369294	in-del	-/AAG			intron-variant	Phf2	GRCm38.p3	13:48846250	GAGGAGGAGAAGGAG[-/AAG]GAGGAGGAGGAGGAG	18676
rs387373729	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48827814	TCAAGGTTTCTCTGT[-/T]CTTTGCTGCTGCACA	18676
rs387394704	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48844345	AATTAAATTTTGTTT[-/T]GTTTTGTTTTGTTGT	18676
rs387394737	snp	A/T			intron-variant	Phf2	Mm_Celera	13:48829659	AACAAATAGAAAGTC[A/T]CACACACACACACAC	18676
rs387396938	in-del	-/AAA			intron-variant	Phf2	Mm_Celera	13:48856581	CCAGGAAAAAAAAAA[-/AAA]TTCAACTCACTATAG	18676
rs387435850	in-del	-/TA			intron-variant	Phf2	Mm_Celera	13:48842133	TGTAATTTACAGTCA[-/TA]GAAAAGTCCACCACA	18676
rs387444136	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48835651	TAGATGAAGGACAGA[A/C]CATTCTCTCAAAGCC	18676
rs387459735	in-del	-/TGTGTTTGT			intron-variant	Phf2	Mm_Celera	13:48838856	GTGTGTGTGGGGGGG[-/TGTGTTTGT]GTGATATACTGTATG	18676
rs387483034	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48823368	ATTGACTCTACCCCC[-/C]AATAAAGAGGGGTAA	18676
rs387499739	in-del	-/CA			intron-variant	Phf2	Mm_Celera	13:48847688	AAACACACACACACA[-/CA]TATATACAAACATAC	18676
rs387536660	in-del	-/GCTTTTTAGGGCCCGAAAAC			intron-variant	Phf2	Mm_Celera	13:48835738	GTCCCTCCCAAGAGC[-/GCTTTTTAGGGCCCGAAAAC]CTGCTCAGAAGCTTC	18676
rs387546925	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48848967	GGGCAGGCGGGCAGG[C/T]GGGCAGGCAGGCAGG	18676
rs387548600	in-del	-/CA			intron-variant	Phf2	Mm_Celera	13:48808844	ACACACACACACACA[-/CA]ATCTCTATCTGTATC	18676
rs387555803	in-del	-/GGAGGGAGGGAGGGAGAGAGAGAGAGAGAG			intron-variant	Phf2	GRCm38.p3	13:48861904	GAGGGAGGGAGGGAG[lengthTooLong]AGAGAGAGAGAGAGA	18676
rs387562599	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48807164	AAAAGTCACATTATA[C/T]GATCCATTTAGATGG	18676
rs387588839	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48825003	CGTGTGATGGAAGTG[C/T]TGTGTGTGACGTTAG	18676
rs387600858	snp	A/T			intron-variant	Phf2	GRCm38.p3	13:48842685	GTGTGTGTGTGTGTG[A/T]GAGATATGTGTGCAC	18676
rs387608055	in-del	-/TGGGGTAGCTC			intron-variant	Phf2	Mm_Celera	13:48824272	CCTGACCAGGCTGTC[-/TGGGGTAGCTC]CGTATAACCTGATCC	18676
rs387632031	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48821203	ACTTCAATCTCAAAA[-/A]TGTGGTCAAATTACG	18676
rs387663948	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48854996	CCCATGGGAATGCAT[-/T]ACCAGAGTGGTACTC	18676
rs387669950	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48850802	GCATGAGCCTGCAGC[C/T]GAAGGCCAGGAACGA	18676
rs387686574	in-del	-/GA			intron-variant	Phf2	Mm_Celera	13:48844009	ACTCAAACACAAAGA[-/GA]TCTTGAGAAAGGCTG	18676
rs387698334	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48837257	GCATATACATACACA[C/T]AGACACACACTGAAT	18676
rs387724437	in-del	-/C			intron-variant	Phf2	Mm_Celera	13:48819713	GAGGCCACTGCCCCC[-/C]AGACCACTCGCCCAA	18676
rs387726324	in-del	-/CT			intron-variant	Phf2	Mm_Celera	13:48858617	TCTCCCTGAGCCTCT[-/CT]ACCATTCAACCCAGG	18676
rs387730623	in-del	-/AGA			intron-variant	Phf2	Mm_Celera	13:48846666	AGCCCCTCATGAAGA[-/AGA]TCTCTTGATGGCCGT	18676
rs387740689	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48861880	AAGGAAGAAAGGAAG[A/G]AAGGAAGGGAGGGAG	18676
rs387755205	in-del	-/CA			intron-variant	Phf2	Mm_Celera	13:48867090	ACCAAATGGACCAGA[-/CA]TGATACCTGAGGGCG	18676
rs387760273	snp	G/T			intron-variant	Phf2	GRCm38.p3	13:48816638	AGCAGAGGAGACCAG[G/T]CACTCCTGCTGTCCA	18676
rs387760764	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48854979	TAATCAGAGGAGCTG[C/T]TCCCATGGGAATGCA	18676
rs387760783	in-del	-/GT			intron-variant	Phf2	Mm_Celera	13:48812705	GGCTCACACCCATCT[-/GT]ACAGCTACAGTGTAC	18676
rs387772382	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48868249	ATGGGTAGGTTAGAG[A/G]ACATCTTGCATCTAG	18676
rs387795828	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48827946	TTTTATGTGGGTCCT[-/A]GGGATGCAAGGTCAT	18676
rs387821369	in-del	-/T			intron-variant	Phf2	Mm_Celera	13:48827934	AACACATTAGCTTTT[-/T]ATGTGGGTCCTAGGG	18676
rs387852013	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48847727	CATACCACACATACA[C/T]AGACACAAACATACA	18676
rs387877572	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48846266	GAGGAGGAGGAGGAG[A/G]AGGAGGAGAAGGAGA	18676
rs387885948	in-del	-/A			intron-variant	Phf2	Mm_Celera	13:48845736	CAGCAACCATTAAAA[-/A]TGCTTATTTTGAAAA	18676
rs387894062	in-del	-/AC			intron-variant	Phf2	Mm_Celera	13:48822035	CAGGGGATACAGCCC[-/AC]TAGGAGCTGGGGCAC	18676
rs578543726	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48841166	AAGGGAGAAGCCTCC[A/G]GTCCCTCCAAGTTCA	18676
rs578573557	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48823528	GAGACCCCCCCACCC[A/C]CCTCACCCCAGTCAC	18676
rs578647520	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48857180	GTGTTTAGTTTATCG[A/C]AGCTCGAGGTGTGTC	18676
rs578697619	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48833716	CCTGAGATGAGCACA[C/T]ACCCTTTACCCCCAT	18676
rs579098153	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48831222	GATATGGGAAGAAGT[C/T]GGCAGGATTTCTTTG	18676
rs579117967	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48809988	GTACCCCCTCCAGCA[C/T]AGTACCCCCTCCAGC	18676
rs579119419	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48848518	CCAGCACTGAGGACG[C/T]AGTGAAAGAAGAGAA	18676
rs579256059	snp	A/G			upstream-variant-2KB, nc-transcript-variant	Phf2, LOC102642832	GRCm38.p3	13:48872529	AGTAGCCTACCAAAG[A/G]TGGGGGCAGAGGGAG	18676
rs579315360	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48820387	AGGTTGTTCCTAGCC[A/C]AGAGCATGGAACCTA	18676
rs579318350	snp	C/G			intron-variant	Phf2	GRCm38.p3	13:48854686	CCCCCCCCCCCCCCC[C/G]AAAGAGAAAAGGAAA	18676
rs579747130	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48825350	GCATCCACGAGTGCA[C/T]TGAGTGTGAGTGGGT	18676
rs579774294	snp	A/C			downstream-variant-500B	Phf2	GRCm38.p3	13:48801400	AGGGTGCTTATGGGG[A/C]TGGGAGAGCAGAGGG	18676
rs579776351	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48846245	GAGGAGGAGGAGGAG[A/G]AGGAGGAGGAGGAGG	18676
rs579781758	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48863645	AGCCGGCAGAGGAAC[A/C]AGTCAAAACCACCGC	18676
rs579851028	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48810201	CCAGCACAGTACCCC[A/C]TCCAGCACAGTATCC	18676
rs579908703	snp	G/T			intron-variant	Phf2	GRCm38.p3	13:48844356	GTTTTGTTTTGTTTT[G/T]TTGTTTTTGGTTTTG	18676
rs579999681	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48848976	GGCAGGTGGGCAGGC[A/G]GGCAGGCGGGCAGGC	18676
rs580049311	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48813602	GGACTGAGCAAGACC[A/G]TGTCCCTCTTGTGCC	18676
rs580053358	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48851464	ACTTAGGGAGCAGAG[A/G]CAGGCAGATCTCTGG	18676
rs580335202	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48812710	CACACCCATCTACAG[A/C]TACAGTGTACTCATA	18676
rs580354466	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48849040	GGCAGGAGGGCAGGC[A/G]GGCAGGAGGGCGGGC	18676
rs580418326	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48846257	GAGAAGGAGGAGGAG[A/G]AGGAGGAGGAGGAGG	18676
rs580469333	snp	G/T			intron-variant	Phf2	GRCm38.p3	13:48839346	ATAAAGCCCCACCCC[G/T]TCCTGAGGAACTCAC	18676
rs580519606	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48808598	CCTACAACCCATCCA[C/T]GCCTACACCCCTATC	18676
rs580528164	snp	A/T			intron-variant	Phf2	GRCm38.p3	13:48824289	GGGTAGCTCCGTATA[A/T]CCTGATCCTCTGTAT	18676
rs580538535	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48862803	ACATGATAGTGTGCA[C/T]GCACACACACACACA	18676
rs580603444	snp	C/G			intron-variant	Phf2	GRCm38.p3	13:48827941	TAGCTTTTTATGTGG[C/G]TCCTAGGGATGCAAG	18676
rs580978593	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48865786	TCCCCATATTCAGTA[C/T]CAGAGACTCTGCTAG	18676
rs580995417	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48852586	TGTGTGTGTGTGTGT[A/G]TGTATGTATGTGTGT	18676
rs581001552	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48806247	CACTCTATCTGAAGT[C/T]CCAAGACCCTCCCAA	18676
rs581045936	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48847227	AAAAAGATAGCAGTT[A/C]CCAGGGTTTGGGTCA	18676
rs581159333	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48840337	AAGTCTGAGAGACGG[A/G]TGGCAAGTGGGGTGC	18676
rs581164415	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48839352	CCCCACCCCTTCCTG[A/C]GGAACTCACTGATGG	18676
rs581266887	snp	C/G			intron-variant	Phf2	GRCm38.p3	13:48822625	TGCTTCAGTGGTGAG[C/G]CCCTAACCCTCATGT	18676
rs581595423	snp	C/G			intron-variant	Phf2	GRCm38.p3	13:48852900	TCTCCAGCTGGGCTG[C/G]GCTTCCCTTCCCCGA	18676
rs581702573	snp	C/G			intron-variant	Phf2	GRCm38.p3	13:48868983	AAATCCTCAGAGAAA[C/G]AGTAAGGTGACTAGA	18676
rs581757891	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48830144	TTATACACACACACA[C/T]ACATACATACATACA	18676
rs581785069	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48848980	GGTGGGCAGGCAGGC[A/G]GGCGGGCAGGCAGGC	18676
rs581922365	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48861963	AGAGAGAGAGAGAGA[A/G]AGAAAGGGAACAAAG	18676
rs581979491	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48824197	TCGCTGCCTCAGGCC[A/G]AACAGGCCTCTCATG	18676
rs582142130	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48858621	CCCTGAGCCTCTACC[A/G]TTCAACCCAGGCTGT	18676
rs582305322	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48823242	TTCCACATTCTACCT[C/T]GTAAATCTGCAGGCC	18676
rs582373458	snp	G/T			intron-variant	Phf2	GRCm38.p3	13:48844365	TGTTTTGTTGTTTTT[G/T]GTTTTGGTTTTTTTT	18676
rs582728989	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48847819	ATATACAAACATACA[A/C]ACATACATACCACAA	18676
rs582821343	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48841364	TAGAAAAATCGGGCT[A/G]GTGAGATGGCTCAGT	18676
rs582871394	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48815718	TGTTGGAGGATATGA[C/T]GTAATGTGTGTGTGT	18676
rs582876062	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48809943	CCCTCCAGCACAGTA[C/T]CCTTTCCCGCACAGT	18676
rs582918267	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48846248	GAGGAGGAGGAGAAG[A/G]AGGAGGAGGAGGAGG	18676
rs582936711	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48835726	CAGTGACCAGTGTGT[C/T]CCTCCCAAGAGCCTG	18676
rs583037890	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48852590	TGTGTGTGTGTATGT[A/G]TGTATGTGTGTGTGT	18676
rs583158508	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48828153	GTCACCAATGTCACC[A/G]GGGATGGATCAAACC	18676
rs583164761	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48864804	AGGGTCAGGAAAGCC[A/G]ACTGTGACAGAGACT	18676
rs583338016	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48863659	CCAGTCAAAACCACC[A/G]CTAAACACAACTCCA	18676
rs583387548	snp	G/T			intron-variant	Phf2	GRCm38.p3	13:48804849	TCTACCAGGTAGGAA[G/T]CAGGGAGGGGAGGGG	18676
rs583513673	snp	C/G			intron-variant	Phf2	GRCm38.p3	13:48826298	TGCCTTTGTGCATGG[C/G]CGTACCACACCCCCA	18676
rs583645276	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48824693	TGTGTGATCTCCAGG[C/T]TTGCTGTCTCCCAAC	18676
rs583653342	snp	A/T			intron-variant	Phf2	GRCm38.p3	13:48862824	CACACACACACACAC[A/T]CACACACACACGCAA	18676
rs583764970	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48815236	TGTGCCTTGCCCTGC[C/T]CCACTGGCCACCGGG	18676
rs583885163	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48849055	AGGCAGGAGGGCGGG[C/T]GGGCGGGCAGTCTGG	18676
rs584042563	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48812753	TAAATCTTTAAAAAA[A/G]AAAAAAAGAGTCAAA	18676
rs584198939	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48866273	GAGGAGGGAGGGAGG[A/G]AGGGAGGGAGGGAGG	18676
rs584301398	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48809229	GGCTCTCAGACAGGA[C/T]CCGGCTCTGACTTCT	18676
rs584414313	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48833247	AGAACACAGGCACCC[C/T]CTGCACAATCACTCC	18676
rs584766740	snp	C/G			intron-variant	Phf2	GRCm38.p3	13:48847246	GGGTTTGGGTCAAGT[C/G]AAAGGGGGAATTGAT	18676
rs584854429	snp	G/T			intron-variant	Phf2	GRCm38.p3	13:48864820	ACTGTGACAGAGACT[G/T]GCTGCCTCTGGATCA	18676
rs584892119	snp	C/G			intron-variant	Phf2	GRCm38.p3	13:48830716	CACAGACTGAGAGAA[C/G]CCTGCTCCACCACGG	18676
rs584961415	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48856563	GAGGCAAAGGCAGAA[A/G]GGCCAGGAAAAAAAA	18676
rs584986831	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48822629	TCAGTGGTGAGCCCC[C/T]AACCCTCATGTAGCC	18676
rs585020285	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48841554	AGAAAAATCACACTT[A/G]CAGGTTTATTTAAAA	18676
rs585239870	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48848988	GGCAGGCAGGCGGGC[A/G]GGCAGGCAGGCGGGC	18676
rs585341634	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48818579	CTGGGAGCCACCTCT[A/G]CTAGTGGAAAACGCA	18676
rs585347738	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48854665	TATCACAAACCTCCC[C/T]CTCAACCCCCCCCCC	18676
rs585429001	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48858747	TGCAGATGCTTGTGT[A/G]CAGCTGTGGGTCAGG	18676
rs585495166	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48812700	GATGAAGGCTCACAC[C/T]CATCTACAGCTACAG	18676
rs585599706	snp	G/T			intron-variant	Phf2	GRCm38.p3	13:48835601	TGGGTGGGTATGGCG[G/T]ATCTAGAAGGCAGTG	18676
rs585611818	snp	A/G			upstream-variant-2KB	Phf2, LOC102642832	GRCm38.p3	13:48871031	GGGGGGCCCGGCCGC[A/G]CGCGGGACACAAAGC	18676
rs585664648	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48810200	TCCAGCACAGTACCC[C/T]CTCCAGCACAGTATC	18676
rs585670723	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48848972	GGCGGGCAGGTGGGC[A/G]GGCAGGCAGGCGGGC	18676
rs585684667	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48835728	GTGACCAGTGTGTCC[C/T]TCCCAAGAGCCTGCT	18676
rs586234618	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48826305	GTGCATGGCCGTACC[A/G]CACCCCCAGGACAAA	18676
rs586264113	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48863179	GGATGGTTATCAAGA[A/C]CATGCCAAGTTAGCC	18676
rs586309378	snp	A/C			intron-variant	Phf2	GRCm38.p3	13:48824204	CTCAGGCCAAACAGG[A/C]CTCTCATGCCTCTAC	18676
rs586313379	snp	C/G			intron-variant	Phf2	GRCm38.p3	13:48862355	TGACCTACACACACA[C/G]ACACACACACACACA	18676
rs586343701	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48852620	TGTGTGTGTGTGTGT[A/G]TGTTTTATTTGTTTT	18676
rs586613730	snp	A/T			intron-variant	Phf2	GRCm38.p3	13:48863984	CACCCAGACAGGAGA[A/T]TATTATTCAGCCATT	18676
rs586749497	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48839153	AGGTATTAGAAGAAA[A/G]CATGAATGAACTCCT	18676
rs586828685	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48840229	TTTACACATTCAGCA[A/G]CACAGATGAATGGGA	18676
rs586974012	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48815260	CACCGGGCTCAGAGG[C/T]GCTGAGTCCTGGCCC	18676
rs586982093	snp	C/G/T			intron-variant	Phf2	GRCm38.p3	13:48852511	TCCTTGCCCTCTCTC[C/G/T]CTCTCTCTCTCTCTC	18676
rs587087391	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48847700	ACACATATATACAAA[C/T]ATACACACATACATA	18676
rs587348893	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48864811	GGAAAGCCGACTGTG[A/G]CAGAGACTTGCTGCC	18676
rs587365932	snp	C/T			intron-variant	Phf2	GRCm38.p3	13:48828601	TGTGGCCATTCGTGC[C/T]GGAACAGCCACAGGA	18676
rs587397512	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48846251	GAGGAGGAGAAGGAG[A/G]AGGAGGAGGAGGAGG	18676
rs587400333	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48846953	ATCTGCCCAGGGAGA[A/G]CTGAAAATTCACACA	18676
rs587418698	snp	A/G			intron-variant	Phf2	GRCm38.p3	13:48804928	GGAGGGGAGGGGAGG[A/G]GAGGAGCTGATGAGG	18676
rs864263260	in-del	-/T			utr-variant-3-prime	Phf2	GRCm38.p3	13:48801776	CTGAAATATTTTTAC[-/T]TTTTTTAAAACTTTG	18676

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