EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS091-08828 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr11:118065130-118067440 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr11:118067379-118067393AGCCACGCCCACCA+6.09
SP1MA0079.4chr11:118067377-118067392CCAGCCACGCCCACC+6.27
SP3MA0746.2chr11:118067379-118067392AGCCACGCCCACC+6.78
SP4MA0685.1chr11:118067377-118067394CCAGCCACGCCCACCAC+6.04
SP8MA0747.1chr11:118067380-118067392GCCACGCCCACC+6.62
Sox3MA0514.1chr11:118065499-118065509AAAACAAAGG-6.02
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_28986chr11:118065065-118066748Fetal_Intestine_Large
SE_28986chr11:118067107-118068176Fetal_Intestine_Large
SE_35395chr11:118064424-118066958HepG2
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr11118065482118066498
chr11118067135118067194
Number: 2             
IDChromosomeStartEnd
GH11I118194chr11118064725118066852
GH11I118196chr11118067108118068176
Enhancer Sequence
TGCTGTGGGG GAAGGGCAGA AAGAAACAAA ACATGCTTGT AAGAAGTAGT TCCATAATCA 60
TAGCAGCTGC TGTTCATTGA GCTCTTCTCA TGAGCCCGGC CCAGTACTGA ATTTCATATG 120
CATTATCTCA TGTGATCCTT ACCACCAGGA GGTAGGTATT ATTATTGCCT TTCTAAGGAT 180
AAGGAAACTG AGGCTCAGAC AGGCCAAGTT ACTGCCCAAG ACCATCTGGC TGCAACACAG 240
AGTTAGAATT TGGACCCAGG TCTGTCTAAC TCCACAGCTT GTGATCTTAA CCTCTGTGTG 300
TACAGCCTCA GAAAGGGAAA ACAGCAAGGT GCCACTACAT TTACATGAAT TTCATCAATT 360
CAACAACAAA AAACAAAGGC TCTTTGTTAC CCCTGCTCCC TATCAGAGAA CACCTTTATA 420
AATGCAGTCT CAAACAAGTG GCCTGCAGTC CCAAATTCAC CAACAGCCTT ATTTAACTTG 480
GCACATCATA TTTTAAAATA ACTTGACTGG CCCCTGCCAG CCTTTGAGTT TGCAGCCCAG 540
GCCTCTTCTC TTACTCTATT GGATCTAGAT CAAGAGGACA GGAATGGTGT TTTCAACAGA 600
ATCAAAACCA TAATCGCCTA GCATTAAACC TGGGGAAGTT AGCTGTGAAG ACAATTGTTC 660
CTCCTGCATC ATCTCCACCT CGGAGACGTT CTGCAAACAG TGCCACCCTG GCTGGTGACC 720
CACTCAGCAG TAGCCACAAG GCAGCTGTAT CAGCAGGTCT CCAGGAGCCA GGATGAGGCC 780
TCGCAAGTTA CTGCAGCATC ACATAACAGT ATGGGAGAAA GATACAGAGG GAAAATGATT 840
CCATTCAGCT GCAACTTCAG GGTGGAGTTA ATGTTTCACT CGGTGGATCC AGGCCAGGCC 900
TCTGATCTCA CACTTCCCTG GCAGACCTCT CTCTGCTGCA ATCAGCTGGG AGTCATGTGT 960
CCTCAGGGCT GGTACGATAG GAACAAACAA AGCCCATCAT TCCACAAGCA GAGGAGGCCA 1020
GCCTTCCCAA ACCCACAGAA CACTGCTCCT TAATAGGCTG GGTGCCTATA ATTAGTCTAC 1080
AAATAGCACC GTGCTCATCG CCAGCTCACT CCTTTTGTCC CTACCCCCAC TCACTGCACG 1140
CCCCGAGGTG CCTTTTCCAG GCACTGCAGT TCTCTAAGGG GCTACAGAAG TCTAAGCAAA 1200
GGGAAATTAG GAATCAGACT CCAAAATATT GTATGAGATC CAGCATGCAG CCTGCCTGGC 1260
AGTTAGGTTA TGAGAAGGTA TAATAAGTCA CAAAGTTAAG AAACAAAATC TAAGCATTGG 1320
AAGGAACCCT ACTTTGACCT TTTGATAGCA AGGAAAACGA CTCACAGCAA CACAATACTT 1380
GCCCAAGGAT CTTATCCTAT TTATCCTATT TTCTTTGTTG TTGTTGTTGT TTTGAGACAG 1440
GAGTCTCGCT CTGTTTCCCA GGCTGGAGTG CAGTGGCGCG ATCTTAGCTC ACTGCAACCT 1500
CCACCTCCCA GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC CAAGTAGCTG GGATTACAGG 1560
TGCCCGCCAC CATGCCTGGC TAATTTTTTT GTATTTTTAG TAAGACAGTG TTTCACCATG 1620
TTGGCCAGGC TGGTCTCAAA CTCCTGACCT CAAGTGATCC ACCTGCCTCA GCCTCCCAAA 1680
GTGCTAGGTT TACAGGTGTG AGCCACCATG CTCGGCCTTT TTTTTTTTTT TTGAAACAGA 1740
GTCTTACTCT GTCTCCCAGG CTGGAGTGTA GTGGTGGATC TCGGCTCATG TAACCAACGC 1800
CTTCCAGGTC CAAGCAATTC TCGTGCCTCA GCCTCCCAAG TAGCTGGGAT TATAGGCACG 1860
CATCTCCACA CCTGGCCAAT TTTTGTATTT TTAGTAGAGA GGGAGTTTTG CCACATTGGC 1920
CAGGCTGGTC TTGAACTCCT GGCCTCAAGC AATCCGCCCA CCTCGGCCTC CCAAAGTGCT 1980
GGGATTTCAG GCATGAGCCA CCACACCCGG CCGTGTTTTC TTTATTAGAT TGAACTGATG 2040
AGGCAAAAGA CGTCCTCCCT GCCCTCAGTA AAAGCCACTC TTCACTTCTT TTCACCACTA 2100
ATATAAATAA TCTCTGGTGA TAACCTTTAA TCCTTGAGCT TGGGTAAGAA AGTTTGATAT 2160
CACTCTTCTA TCCAGCAGAA CTTCAGTTTC TCAGACTTTT CTGCTACTTA GAAAAATCAC 2220
CGCCCTCAGC AGCCTCCCTT GGGCAACCCA GCCACGCCCA CCACCACCAC CACCTGAGCC 2280
TCTGACACCT GGCTCAGCTG AGGCCAGAAT 2310