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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS073-02502
Organism
Homo sapiens
Tissue/cell
GM19238
Coordinate
chr11:65636100-65637320
Target genes
Number: 34
Name
Ensembl ID
POLA2
ENSG00000014138
AP000769.1
ENSG00000173727
MALAT1
ENSG00000251562
SCYL1
ENSG00000142186
LTBP3
ENSG00000168056
RP11
ENSG00000260233
SSSCA1
ENSG00000173465
FAM89B
ENSG00000176973
EHBP1L1
ENSG00000173442
MAP3K11
ENSG00000173327
PCNXL3
ENSG00000197136
SIPA1
ENSG00000213445
RELA
ENSG00000173039
KAT5
ENSG00000172977
RNASEH2C
ENSG00000172922
AP001266.1
ENSG00000175827
AP5B1
ENSG00000254470
OVOL1
ENSG00000172818
SNX32
ENSG00000172803
MUS81
ENSG00000172732
CFL1
ENSG00000172757
EFEMP2
ENSG00000172638
FIBP
ENSG00000172500
CCDC85B
ENSG00000175602
FOSL1
ENSG00000175592
C11orf68
ENSG00000175573
DRAP1
ENSG00000175550
SART1
ENSG00000175467
BANF1
ENSG00000175334
EIF1AD
ENSG00000175376
SF3B2
ENSG00000087365
PACS1
ENSG00000175115
RAB1B
ENSG00000174903
MRPL11
ENSG00000174547
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr11
65636460
65636709
Enhancer Sequence
CTGAGGAAGC ATGGGGATGG GGACCCCGGG TCAAGGGCAT TCCTCACCAT TCAGTCCCAC 60
AAACATTTCC CAAGAAGGCC CAGCCCCATG TTAGACTGAA TGTAGGAAGA CAGAGGGGGA 120
TGAGACAAGC CACAAGTTCA GCCGGGAGAT GGAGGGTTCA AAGAAAGTTT GCCCAGGCTG 180
CCGCAGCTCA CAGACTTCTC TCTGCCCAGA ACTGGAAGAA ACACTAAATA AGTTACTGGG 240
AATCTAGAGG CTTGGGTGTG AATCCCACCA GCTGATCTAG GGGAATCTCA TTTTCCCAAT 300
CAGTAAAATG AGTGTGTTAG ACTAGATGAG TCTTATGGGT CTGGCTTGTG CTGTAACGCC 360
CAATTCCTGC AACCCACAGT CAACCTGAGC ACCCAGTGGT CACCTCCAAC TAACTGTGAG 420
CTTCACAGGC AGAACATTTC CTTTCTCTTG TTCCCCTCAT GCTGCCAGGT AGCAGTGAGG 480
CCTCATCCCG CAGCAAAGCA TAACATAGGG GGTACATGCC AGTTTACAGG GTGTAAGAAG 540
TCTGGGATCC AGCCCTGGCC CCATCTCATC CTGGCTGTAT GAGCTTGGGC GGGTCACTTA 600
ACCTCTCTTA GCTGAATCAT GAAAGTCACC ATTTACCCAG GACTTTGTGA TTATTTTTAT 660
GTAATCCTCC CAACAAACGT GGAGGGAGAT ATGAATGTCC TCATTTTGTA GAGGAAGGAG 720
AAAATCATAC CTCCTAGGAT TCTTGAGAGG AAGGAGGCCA AGTGTGTCAG GGAATACACT 780
ACGAGGGCAG GTTCTCATTA AGTGGCAGTT CATTCACTTT AAAGCACTGC AGCTTGAGAC 840
TTGCTGGAGC CCATCTATCA CACTCTCACC TAATCCTCAA GACAACCCAT TTTATAGAAG 900
AAGAAACAGG CTCAGAGAGG AGTGACTTGT CCTAGTGCAA AATTCAAATG CAGGTAAATG 960
CAGGTGAGCC TGATATGTGG GACAGGTGGC ACCCACATCC TCAGTCTCAC CAGTAGGCTT 1020
CAGTAAGGAC GTAGCTGCCT CTCCTTGTGC CTCCCCCACT AGCCTGGGAG TGCTCCACAG 1080
CCAGCCGGGG TCGAGTACCC AGGAGGCAGC TGGGTGCACA GTGACAGGAG GCGGAGGCCT 1140
CAAATGGAGA ACTGTGTGGC AGGAGGCACG GCATAGCTAG GGCCTGGGGG TCCACAGAGG 1200
AGTACACAGC AGGGATGGAG 1220