EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-39399 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr5:149033400-149036020 
TF binding sites/motifs
Number: 36             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PPARGMA0066.1chr5:149035779-149035799AGGAAGTAACAGTGACCTAG-6.57
RREB1MA0073.1chr5:149034431-149034451CCACACACCACACACACCAC+6.01
RREB1MA0073.1chr5:149035137-149035157CCACACACCACACACACCAC+6.01
RREB1MA0073.1chr5:149034547-149034567ACACCACACACCACACCACA+6.05
RREB1MA0073.1chr5:149034555-149034575CACCACACCACACACACACC+6.11
RREB1MA0073.1chr5:149035283-149035303CACCACACCACACACACACA+6.11
RREB1MA0073.1chr5:149035303-149035323CACCACACCACACACACACA+6.11
RREB1MA0073.1chr5:149035323-149035343CACCACACCACACACACACC+6.11
RREB1MA0073.1chr5:149034413-149034433ACACACACCACACACACACC+6.16
RREB1MA0073.1chr5:149034689-149034709ACACACACCACACACACACC+6.16
RREB1MA0073.1chr5:149034740-149034760ACACACACCACACACACACC+6.16
RREB1MA0073.1chr5:149034764-149034784ACACACACCACACACACACC+6.16
RREB1MA0073.1chr5:149034815-149034835ACACACACCACACACACACC+6.16
RREB1MA0073.1chr5:149034826-149034846ACACACACCACACACACACC+6.16
RREB1MA0073.1chr5:149034850-149034870ACACACACCACACACACACA+6.16
RREB1MA0073.1chr5:149034863-149034883ACACACACCACACACACACA+6.16
RREB1MA0073.1chr5:149034898-149034918ACACACACCACACACACACC+6.16
RREB1MA0073.1chr5:149035254-149035274CCACACCCCACACACACACC+6.16
RREB1MA0073.1chr5:149034880-149034900ACACAAACCACACACCACAC+6.25
RREB1MA0073.1chr5:149034957-149034977CCCCCACACACACACCACAC+6.26
RREB1MA0073.1chr5:149035028-149035048ACACACACCACACACACCCC+6.37
RREB1MA0073.1chr5:149035164-149035184ACACACACCACACACACCCC+6.37
RREB1MA0073.1chr5:149034993-149035013CCACCACACACCACACCACA+6.55
RREB1MA0073.1chr5:149034402-149034422CCACACACCACACACACACC+6.68
RREB1MA0073.1chr5:149034483-149034503CCACACACCACACACACACA+6.68
RREB1MA0073.1chr5:149034638-149034658CCACACACCACACACACACC+6.68
RREB1MA0073.1chr5:149034656-149034676CCACACACCACACACACACC+6.68
RREB1MA0073.1chr5:149034887-149034907CCACACACCACACACACACC+6.68
RREB1MA0073.1chr5:149035008-149035028CCACACACCACACACACACC+6.68
RREB1MA0073.1chr5:149035153-149035173CCACACACCACACACACACC+6.68
RREB1MA0073.1chr5:149035191-149035211CCACACACCACACACACACA+6.68
RREB1MA0073.1chr5:149034940-149034960ACACCAACCACACACACCCC+6.86
RREB1MA0073.1chr5:149034936-149034956ACACACACCAACCACACACA+6.98
ZNF263MA0528.1chr5:149033969-149033990CCCCTATCCTCCCCCTGCCCC-6.37
ZNF263MA0528.1chr5:149033963-149033984TCCCTTCCCCTATCCTCCCCC-6.45
ZNF263MA0528.1chr5:149033960-149033981CCCTCCCTTCCCCTATCCTCC-6.7
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5149034041149034561
Enhancer Sequence
TTTTAGACAT TAAGTGTCAT GAACAATTGA TCACAACTCA GTCGCTGTAG TGCAAAGCAG 60
CCATAGATAA TACATAAGTG AATAGGTGTG ACTGTATGCA ATAATGCTGT ATTTATGGCC 120
ACTGAAATCT GAAATTCGTA TCATCTTCAG TGTCATAAAA CTGTACCCTT CTTTTGATTT 180
TCCCCCCAAC TATTAAAAAA TATAGAGTCC ATTTTTAGTT CACAGGTCAT ATGAAAACAG 240
GTGGCAGCCG GATTTGGCCT GCAGGCTCTA CTTTGCTCAC TCTGCTTTGT GCTGTGCGAC 300
TGCCCTCACC TGCTCCTTAT AGCTCACCTC CTTATTATCT CCATCTCCAG ATAAAGACGT 360
GAAATTTCAA GAGGCTATGA CTTACCCAAG GTTACCTAAT GAGCAGGTTG GGGAGTTGGG 420
ATTTGCAACC AGGTTTGTCT TGTCTCCTGC AGGGGCAGGA GTGCTGGTGC AGGGGGGCAG 480
GAAGCAGGGC TGAGCTGGGG GTTTCAGCAC AGCCTAACTC GGCCTGAAGC CAACAGTCCA 540
CCAAGAGCTG GCAGAACCTC CCCTCCCTTC CCCTATCCTC CCCCTGCCCC CTGCAACCCC 600
GAGAACTGAG TGCAGTAACC AGGGGCCTCT CTGCTCTGTT CTGCCACCAT GGTCCCATTG 660
TCACACCCTC CTGGGATTTG TAAGCAGCTG AAACGCTCTG CTTTCCAAGT CTGGAATCAG 720
AGCCCCAGAA AAACCCAGAG GCCATCTTGA CTTGGTCCAT TCTTGCCAAC CACAGCCATT 780
AAGGAAGGGA AGACCTGGTT TAAAAGGGCC CTGAGCTGCC ACCCGTGAAA CACTTCAGCT 840
CTGGTCCAGC CAAGTCTGGG AAAAGGTTGG GGAAAAGTGA GGGAGGGGAA GAGACAGAGA 900
AACAGAAGGG GAGAGAGGAG AGAGAGAATA AGCAGAAGAG ACGGTGACAA AGAGGCCACA 960
CACACCACAC GCACACCACA CACACCACAC ACCACACACA CGCCACACAC CACACACACA 1020
CCACACACAC ACCACACACC ACACACACCA CACACCTCAC ACACACACAC CACACCACAC 1080
ACACCACACA CCACACACAC ACACCACACG CACACCACAC ACACCACGCA CACCACACAC 1140
ACCACACACA CCACACACCA CACCACACAC ACACCACACA CCGCACACAC ACACTGCACA 1200
CACACACCTG CACACACACC ACACACATAC CACACACACC ACACACCACA CACACACCAC 1260
ACACCACACA CACACCTCAC ACACACACCA CACACACCAC ACACACACCT CACACACACC 1320
ACACACACCT CACACACACC ACACACACCA CACACACACC TCACACACAC ACCACACACA 1380
CACCACACAC ACCTCACACA CACCGCACAC ACCTCACACA CACCACACAC ACACCACACA 1440
CACACCTCAC ACACACACCA CACACACACA CCACACACAC ACACAAACCA CACACCACAC 1500
ACACACCACA CACACACCAC ACACACCACA CACCCCACAC ACACCAACCA CACACACCCC 1560
CCACACACAC ACCACACACA CCACACATGC ACACCACCAC ACACCACACC ACACACCACA 1620
CACACACCAC ACACACCACA CACACCCCAC ACACACACCA CACACACCAC ACACACCACA 1680
CACCACGCCA CACACACCCC CCCACACACA CCACACACAC CACACATACA CACCACACCA 1740
CACACCACAC ACACCACACA CCACACACAC ACCACACACA CCCCACACAC ACCACACACC 1800
ACACACACAC ATCCCACACA CTCCACACAC ACACCATACT CCCATACACA CACACCACAC 1860
CCCACACACA CACCACACAT GCACACCACA CCACACACAC ACACACCACA CCACACACAC 1920
ACACACCACA CCACACACAC ACCACACACC CAGAAAGAGA TCCTTTAAGA GCTGTTTTTT 1980
TCTGGCCCGG AACCGTATTT CATTCTCCAA CTCTGCAGAC ACAGAAAAGG CATTATTGCA 2040
GTAAAAAGTC TCCCCACATT ATTTATTGTT AATACTTACC TACTTTGTCC TCTCTAGGTT 2100
TTTACAGCCT TAACTTCATT CAAAGCAGGC CCCTGGTGTG GGCAATGCAG AGGTTCTTTG 2160
CCTGAGGAGG GATGAGGAGC TCAGAGAGCT CCAGCAACTT GCTCAAGATT GCGCAGCAGG 2220
TTAATGGCCA AGTTGGGACC AAGGATCAAG ACTACCGACT TCCAGTGCAG TGGGAGTCTC 2280
CTACAAACCA TGTCCAGGAT CAAAGCAGAC GCTGAAGGGC AGAGGTTTTG TTTACCCTCT 2340
TCCCTTCAAT TACTGAGTCC CTAAACTCCC TCTTTAATAA GGAAGTAACA GTGACCTAGT 2400
ATATTTGAAC TTGAGCAAGG CAGTGGACAA GCAGGTGCAT GATATTCCCA TGGTCAAGCA 2460
TGATGGAAAA CTGTGAGATG GATTCAAGGG CCGTCAGTAG AAGACTGGCA CCCAAACAAT 2520
TTTGGTGAAT CGGTTTCCAC ATAGAAGGAT GCTTTGCCCC ATGATTTTTT ATTCCTAAAA 2580
TTTAATGACT TGAGCGTCTC TCCCACCTCT TCTTTATTTT 2620