EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-27110 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr2:106361600-106364950 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:106361801-106361819CCTTCCTGCCCGCCTTCC-7.43
Foxd3MA0041.1chr2:106364451-106364463GTATGTTTATTT+6.11
JUNMA0488.1chr2:106364765-106364778ATGGCATCATCTT-6.13
SP1MA0079.4chr2:106362768-106362783GGTGGGCGTGGCTTG-7.91
SP3MA0746.2chr2:106362768-106362781GGTGGGCGTGGCT-6.78
SP4MA0685.1chr2:106362766-106362783CCGGTGGGCGTGGCTTG-6.51
SP8MA0747.1chr2:106362768-106362780GGTGGGCGTGGC-6.62
Stat6MA0520.1chr2:106363157-106363172GGTTTCCTGAGAAGC+6.07
Number of super-enhancer constituents: 21             
IDCoordinateTissue/cell
SE_10292chr2:106361659-106363935CD19_Primary
SE_10292chr2:106364382-106367666CD19_Primary
SE_10910chr2:106358550-106368508CD20
SE_11843chr2:106361914-106367755CD3
SE_14420chr2:106360241-106367719CD4_Memory_Primary_7pool
SE_15409chr2:106361433-106367753CD4_Memory_Primary_8pool
SE_16019chr2:106361544-106365852CD4_Naive_Primary_7pool
SE_16297chr2:106361497-106367758CD4_Naive_Primary_8pool
SE_17053chr2:106361471-106367573CD4p_CD225int_CD127p_Tmem
SE_17337chr2:106361480-106387542CD4p_CD25-_CD45RAp_Naive
SE_17777chr2:106353821-106375306CD4p_CD25-_CD45ROp_Memory
SE_18243chr2:106361552-106379750CD4p_CD25-_Il17-_PMAstim_Th
SE_19126chr2:106359851-106367802CD4p_CD25-_Il17p_PMAstim_Th17
SE_21170chr2:106361531-106367770CD8_Memory_7pool
SE_21696chr2:106361351-106368467CD8_Naive_7pool
SE_21946chr2:106359820-106368483CD8_Naive_8pool
SE_22311chr2:106361687-106368225CD8_primiary
SE_37706chr2:106360079-106367801HSMMtube
SE_43610chr2:106360437-106364008MM1S
SE_53622chr2:106359625-106367802Spleen
SE_62262chr2:106353762-106421483Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2106364522106364900
Enhancer Sequence
CGCGGCTAGG CGGGCGTGGG GCGGGGGCCA CAAACTTGGG GCCGTTGGGC GGAGTTGGGA 60
GCGCGGCGGG GCTCGCGGGC CGGGGTGCGC CCGGGAAGGG GCCAGGAGAG CGGGTCCCCT 120
CCGCGCCCCT CCGGTGCTCT CGGCCCTGCC GCGGCCTGGG CGCCCCCGAC CGCGGACTGC 180
CGGGCACCTC CCGGCTCTGC ACCTTCCTGC CCGCCTTCCC ATCCCTAACC CCCACCATCG 240
GGGGCCGGCC CAGGGGCGGG GACGCCAGCC AAGGGCGCGG GCGAGGATCA GGGCAGGGGG 300
CCCGGCTGCG GGGCCCGGGG ACTGGAGACC CCCGGGTGCG CAGGCTGCGC CTGGCCTGCA 360
GGCGGGCGGC CGGCACGGAG CTCGGGGCTA GCGTGGGACC GTGCGGTGGC CAGGGTCGCC 420
AGGGCGCGTG TGCCGGGGAA GAATAGCCGC GGATCGCAGG GCCCCGGCGC AGGGACGGGG 480
GAGGCCGCGA TCGGCCGGGA GAACTTAACC GTGTTTATTA CAACTATTTA TGTTCGCGCA 540
CAAAGCTGCT GTCACATTGC ATAAAGGAGG TCCTCGCTTC GGCGAAGGGA GCTTTTGTGC 600
CCGGCTTCAG GCTCTGCGCC CTGCCCCAGA TTTACAGGAC TCTAACAGCC ACCTGAATGA 660
ACCAAAGTTT CTCACAATCG CTCGGCTCTC TCGGTTTTTT TCAGGGCGAT TTAATCACCG 720
AGTGCTTTTG GAAAAATTTG ATATGTGAGT TTTAAGGCAT GGAGGGTAAC TGCCTTATGA 780
GCACAGTTAG CTTGGCATTG TGTGGAGGGG TTTAATTTGC AAAACGCTTT AATTTGTAGA 840
CAATGGGGAT CTCTGTGAAG GTCTGCGGTG GATGCTAGGG GTCATTGGCT GGTGGACCCC 900
AGGCACCTGA CTTAAACTAG TATTGTAACA GCTTCAGGGA CAAAGCCGAG CGTGCGTGGA 960
GTCGGCCTTG GCCACTTCAC ACAATTCAGG TTGGCAGATT CCTCTTTATT TGGCTTTGTT 1020
TATTTTGCCA ACAGGTTTAA GGCTGCTTCT GCCAAGTTTG CATCTGCATA ATGGGATGAG 1080
CAGGCCCCAG TGTGGGCAGG AGGGGGCCTA AAATATCGCA AGGGCCAGCT CCGTCCCTCG 1140
ACCCAGAAAG AAACAACCCT GAGAGGCCGG TGGGCGTGGC TTGCTGGGAC CTACAGGTAG 1200
GGGAGTCCCT TCCTGGCCCA GGCGCAGTCC CCGCTTCTCG GAAGGGATTT TGTGTAGGAA 1260
TGAAAGTGAT TCAGGGTGTT TTTCATGCCT CTGTTTTAGA TGTAGTTATC AAGTCTCAAA 1320
AGTGACTGAA AATGAAATTA ACCTGGGCCG CTTTAACTTA CCAAAACGGA ACTGTGCGTG 1380
TGAACACTCC CTCAATTCAC TTTGCAAGCT TCATAGATAA GCAGGTGAAT TAGTAACAGG 1440
ATTCAAGCCT TGCGAGTTTT ACGTAAAGAG AATGGCAGTC ATCGGACACG TGGAGAAGAA 1500
ATTGACTTCA CCTGGAGATT GGGCTAGACA TGGAGGTTTT TTGACGTTTG GAACAGGGGT 1560
TTCCTGAGAA GCAAGTGTTA ACCTGCTTGT GAAGAAGTGA ACACGAGGGA AAATCCTACC 1620
TCAGTATATT CTGCCCTGGA GGTTGGTTAG ATGTAGTTTT GATTGGAGAA GGTGGCGGAA 1680
TCTTAGTGGT CTTCTGGCGG CTACTTGAGG CTGAAATGGA GAACTTTAGG CATAGGAAGC 1740
TGTGGAGGTG CCTGGCCCAC TTCCTGTCCC GGAGGCCTCG CCTGGATTCT GAGCTTCTTT 1800
CCTGCTTCAT AAACATTCAG GGGGGTTGGT CATGAAACAC TGGATGAAAT TGGGTCACAA 1860
ATTGCCATCA GGAAGAGTTG GCTGCTGCAT AACCCCCTCT GTCCACTTGT GGAGAAACTG 1920
ACCCTGTTAA CCGTCGGGCT TGCTGAAGGT GCCTTGCAGG TGGCTGTGCT CAGTTTTCAT 1980
GCTTTGTGTT TTGCTTAGGA CACGCTGCAT ACTTAAATCT TCTTCATCCT TGCTCTGTTT 2040
GACCCTGCCA TATTCCCAGG CTTTGTCATT TACATTTTCG GTTATTTAGC TTTTCCAACA 2100
AACAGCAGAT CTTATGTACA CAGTACTATA TTTGAGAAAT GCACTACCAT CCATATTAAA 2160
TACACCGGAA ATCTTCCTTG CATGTGCACA GACTGGATAA CCTTTTAAAA TACCCTAAGA 2220
CTCCCGGAAT GGCGCAGAAT GCACTGGAGT CCTTTACTTG ATCAGTTGCA CTAGCTTAGT 2280
TTGCCCTGGA TAGACCAGGC TGCGAGGCTC TATGGGACAC CCATTTTTCT AACTGCTCAA 2340
ACTGGCTTGC CGTGTGCACT GGGGGAGACA GGGCTTGCGG AAATCATTCT CTGACATTAA 2400
AAATGAGGCT TAAAGACTGA AGAGCTCAGA ATTGCTTGCT GGAACTACAG GGGAGGATGA 2460
TGAGTGATGT TTGGAAAAAC AAGTAAGCTA ACTTTTTTCA CAAATGAACT GGAAACTCCC 2520
TACAGCTCAC TTCAGATGCT TAGGAAATTA GTTTTCCCAT CCAGAGGGTT TGCGAGTGGC 2580
ACTTCCAAAT GGTTTCTGTT TCCTAAAATG AGTGATGGAA ATACTTCACG GCACGTTTTC 2640
AAAGGGCCTA AGCTAAAATG TGATTTCGTG TATCTTGTTC CATGCCTGAG TTAAGGCAAC 2700
TCAGAAGAAG GTCGTGACGG CCTTTTAACG GGCTATCAAA AGTGTGCAGC TAAAGCAAAA 2760
ACAGTTTTGC ATTTCTTTAG GCCATTTAGT AGCACAATTA AAAAATTAGA CTCTTTTCTT 2820
TTCCTGCATT TTCCTTTGAA CATTTCCCAA AGTATGTTTA TTTCTAAAGG TAAATGAACG 2880
TTAGCAAGTA TTACCTCTGC CCAGTGACAC ACATCCACAT GTGTACTGGC ACATACATTC 2940
CTACCTCAAG AATCTTAGTC CTTGAAACTG TGGAAATGAA AGTTATTTTG ATTGAGGTAG 3000
CAGTGTCACA GTGATGTCAT ACGGTGTCAC TGTCCCTGAC CAGCCTCTGT GTTCCCTCTC 3060
AACTCCTTGG CTCAGTCTCC TCCGTGTCCT GAGTTCTTAC TCATCCCAAG GGTCGTCTCT 3120
TACTTCTTTT CTTCCCCACA TCTTATCAAC TCCAAACTAG AGGGGATGGC ATCATCTTTA 3180
AACTTCCACA GCACTTTCTT TGTGTCCCTG ATTTGTCATC TGTGACATTC TTTCCTGCAG 3240
TTGTTTTTTT TCTTTTTTTA AGGCAGGGTT TCACCCTGTC ACCCAGGCTG GAGTACAGTA 3300
GCATGATCAC AGCTCACTGC ATCCTCGAGC TTCTGGGTTC AGGCAATCTT 3350