EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-46375 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr9:131673230-131676220 
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:131673511-131673529CCTTCCTCCCCTCTTCCC-6.24
Foxd3MA0041.1chr9:131674367-131674379GTTTGTTTGTTT+6.32
KLF14MA0740.1chr9:131674238-131674252GGGTGGGCGTGGCC-6.69
Klf12MA0742.1chr9:131674237-131674252GGGGTGGGCGTGGCC-6.15
Klf1MA0493.1chr9:131675784-131675795TGGGTGTGGCT-6.14
RESTMA0138.2chr9:131673840-131673861TGCCCTGTCCCGGGTGCTGTG-6.28
RREB1MA0073.1chr9:131674986-131675006CGGTAGTGTGTGGGGTGGGG-6.13
SP1MA0079.4chr9:131674239-131674254GGTGGGCGTGGCCTG-7.44
SP3MA0746.2chr9:131674239-131674252GGTGGGCGTGGCC-7.52
SP4MA0685.1chr9:131674237-131674254GGGGTGGGCGTGGCCTG-7.15
SP8MA0747.1chr9:131674239-131674251GGTGGGCGTGGC-6.62
STAT3MA0144.2chr9:131676024-131676035TTTCTGGGAAG+6.02
ZNF263MA0528.1chr9:131673920-131673941TCCCCCACCCCCAGCTCCTCC-6.72
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_01786chr9:131670844-131677719Aorta
SE_02982chr9:131673318-131674904Bladder
SE_02982chr9:131675672-131676234Bladder
SE_03426chr9:131673447-131673893Brain_Angular_Gyrus
SE_03426chr9:131674081-131674559Brain_Angular_Gyrus
SE_07249chr9:131672970-131676358Brain_Hippocampus_Middle_150
SE_15043chr9:131674459-131677196CD4_Memory_Primary_7pool
SE_26602chr9:131672946-131677452Esophagus
SE_31756chr9:131673115-131677345Gastric
SE_36103chr9:131673104-131676522HMEC
SE_38626chr9:131672733-131677091HUVEC
SE_40990chr9:131670925-131677482Left_Ventricle
SE_42380chr9:131670371-131677535Lung
SE_48867chr9:131672896-131676330Right_Atrium
SE_65947chr9:131673076-131674381Pancreatic_islets
SE_65947chr9:131674506-131675933Pancreatic_islets
SE_68883chr9:131672842-131676445H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9131675635131676135
chr9131673400131675472
chr9131673302131675608
chr9131673839131674187
Number: 1             
IDChromosomeStartEnd
GH09I128909chr9131671741131677288
Enhancer Sequence
TGGGCACCTG CTCTGTGTTC GCCCTGTGCC AGGCATGATG CACCTGTCCT CCTTCCACCA 60
ACCTGCTGAG TCCTCCCAAC AGGGTCTGTC TATAGCATCC TCAGGCACGG AGGGAGGTGG 120
CCCCTGGAAT GCCCGGTCTG TCTATAGTAT CCTCAGGCAC GGAGGGAGGT GGCCCCTGGA 180
ATGCCCTGTC TGTCCTCCTG GGCCCCAGGA CAGGACACAC CTTCTCCAGC ATCACTCAGA 240
CTAGATGCTT CAGGCCCTCC AGATGCCTGC TGGCTTGGAA GCCTTCCTCC CCTCTTCCCC 300
AGGGCTCCCT TACTGCAGAG CAACCTGCAA CCCACATGTA TCAGGGATTT TGACAAGTCC 360
TTATCTCCGG CCACCCCATA TTATGACTTG AGCACAGTGG GAGAGTGGAC CAGGGCAGGG 420
TTTTCTCTTG TAGTTTCGGG ACAGGCCCAC TGAATAGGAA AACTGGAGTC CCCTGGGGAG 480
AAGCCACATT TGGGAAGCAC AGAACAAACC CAGCCCTTCT TTAATCTGTG GAGGGGGAGA 540
CCCTGTGGCT TCCCCATAGC ACAGTGCTGC CCTTGATAAG CTGGGACTTC CTCACAGCTC 600
CTGCCATTCC TGCCCTGTCC CGGGTGCTGT GCTGGGGCTG TCCTCCTGGT TGGGGGAGGG 660
TTCAAGCCTC CAGCCTGGCT CCCCATCCTG TCCCCCACCC CCAGCTCCTC CCGCCAAGCT 720
TGCCTGTTAG TGTCATGCCT GCTGGCTGAG GTCACCCCTC AGGAAAGGAG CTGGCGGCAA 780
GCACGCTGTC CCAGAGGAAG GAGACCCTCT GGACACCCTG TTTAGCACAT GGCTTAATCA 840
CATCCTGTCC CCACCCCCTG GAACACCAGA GCCTTAATAG GGAAAACAGT TCACTTGGGC 900
CAACCCCAGG CAGGCCCCTC ATTCTGAGTG GGAGGCCTGA GCCCCTCTTC CTCCTCACTC 960
GGGCTTGATG GCTCCTTCTC AGCCACCTTG GCCAGTGGTG ACCAGGAGGG GTGGGCGTGG 1020
CCTGCCCACG CCCTTGCGTG CTGTTTCTCC AGATTTATAC TCTTGCTAAT GAAAGCCTTG 1080
ACAAGACAGT ATTCATTCGT TCACTCGTTT ACTGATGTGT GCAAATTGTT ATGTTTTGTT 1140
TGTTTGTTTT TTTGGTAGAG ACAGGGTCTC ACTGTGTTTT CTAGGCTGGT CTTTAAACTC 1200
CTGGCCTCAA AGCCTCCCAC CTTGGCCGCC CAAAGTGCTG GTATTACAGG CATGAGCCAC 1260
TTCGCCTGGC CTTTGTGCAG ATGTTTTTTG AGCACTTCTA GAATCCAGCT ATGGAGCAAG 1320
GCGCCGGGGA CATGGGGATG AAGAAGGCCA AGTAACGAGG CAGTTAGCAC AGTGCGTAGG 1380
CGCTCTGCTG GAGCACCAGG TCCCTGGGAA CACAGAGGAA CAGGCCCCTG AAGAACGAGG 1440
AGGAGGAAGC CAGGTGGAGG GGAAAGGGAC AGTCCAGGAG GTTCTGGTGG GGAGGAGCAG 1500
TGAGATGGGC TGCCCAGGAA TGTGGGCATC CTGGAGAGCA GAGGTGGGGC TATGGGGGGG 1560
GGTGTGGATG GCAGGGGGGT CCTGTCCTAC ACCTCAGTTT CAATTGTCTC TTCATTTGTT 1620
TAACAGCCGA TCCCTTGCCA GCCCATAGGC TCTGATGACT AAGACCTAGC TCTTTTGTTC 1680
AAGCAAGTGT TTACCGAATT CCTAGTGATT GAGTGGGTGA AGGAATGAGC TGACTTGCAG 1740
CGTGAGGTTC CTCTTGCGGT AGTGTGTGGG GTGGGGTGAG TGAGAGGTGG GAGGTGGAAG 1800
AGAGCTGTTA AGAGACCACG ATTAGCCATC AGGTGAGGCC ACGGGGCCTG GCGTGGCCAA 1860
GGCAGGTAGG GATGGAGAGA CATGGACGGA TCTGGGAGAC GCTGGAGGGG GAATTCAAAG 1920
GGACGGGAGT TGATGGTGGG GGTGGTCTGA GTGACTTGAG CTTTTTTTTG TGGATTGTTG 1980
AGACTGGAGG AAGCACAGGT TTTCAGAGGC CAAGGTGTGT CTCATGTCAG GTGTCTGGGG 2040
CTCTGGGATG TCCAAGGGAC CATCTTGAAT CCACCTGAAG CCCAAGGAGT CACCCTTTCC 2100
AGGCTCATGG GTGAAGATGG GTCCTTGACT TGCTCACTGT GGAGAGCAGA GAGGGAGAAG 2160
GACAGGAGTC TGCAGAAGAG GAGGGCGAGG CCAGAGCGTG GGGCACATGG GGCCTGGGGA 2220
GTTGGCTGGA TTAGGAACTG GTGACTTTGG CCAGAGAGTT AAGGGTGGAC AGGGTCATGG 2280
AGGCAGAGTG AGGAGAGAGA CAGCGGCTTT CCTGCAGTTG GTCAGGAAGG CCAGAGAGCC 2340
AAGGACAACG CTGGGGCCCT GGAAGCCTCC TGAGAGAGTT GTCCTTTTCA AAGATCAGGT 2400
CGAGTTGAGG CCTTTCAGTG CCGATGGGGA CCCACTGAAG TCTCTGGGGA GGTAGGAGAG 2460
GGTGCAATTG GGGGATTGGG AACCAACTTC AAGCCTCCAG GGCACGGGCC GGCGACAATC 2520
CGACAATCCA GCAGAGAAGG ATCGGTCCAG AGGATGGGTG TGGCTGTGGT GGGAGCCGAG 2580
CAACTGAGAG TACCTCCCCT TTTCTCTCTG GGGCCTGGAG AGGGCTCCCT GGCTCAGAGC 2640
AGGGCATGTT CTGGGGAGGA GGCCTTTCAG GGAGGGGGCT CCAGAGCCAG GCTCCATATG 2700
GACCCGAGCT CTGCCACTCG CTGTCCAGAG CTTTCCCACT GTCCCTGACC ACTGCATGTG 2760
TCAGCAGAGG AGATCACGGG GTGGGAGTGG GGTCTTTCTG GGAAGGCTCT GGCCCCTGGG 2820
TGCTCCAGAG CCCACTTCCT GTCTACCCTC TGACCTTCAG CCCCTGCTGA CCTCAAAGCC 2880
AACCCCAAAT GCATTCCTGA TCCTTGGTCA CAGTGGTGGC AGTGTAGGAT ACACAGGTTA 2940
GGAGCCTTTT TGAAAGCACC CCCTGTGCCT GGGCTGGGCA TGGTGGCTCA 2990