EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS026-00236 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr1:10783480-10786760 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr1:10784249-10784264TGAGAGCAAAGGCCA+6.17
HSF1MA0486.2chr1:10785937-10785950GAATGTTCTAGAA-7.52
MEF2AMA0052.3chr1:10784279-10784291GCTATAAATAGC+6.32
MEF2BMA0660.1chr1:10784279-10784291GCTATAAATAGC+7.22
MYCNMA0104.4chr1:10784259-10784271GGCCACGTGGTC+6.52
MYCNMA0104.4chr1:10784259-10784271GGCCACGTGGTC-6.52
NEUROD2MA0668.1chr1:10785441-10785451GCCATATGGT+6.02
ZNF263MA0528.1chr1:10784826-10784847GGAAGAGGAGGCAGAGGAAGG+6.37
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_23090chr1:10783548-10785045Colon_Crypt_1
SE_24724chr1:10782796-10784169Colon_Crypt_3
SE_24724chr1:10784444-10785540Colon_Crypt_3
SE_26723chr1:10782546-10784344Esophagus
SE_26723chr1:10784380-10784964Esophagus
SE_26723chr1:10784993-10785467Esophagus
SE_26723chr1:10785666-10786401Esophagus
SE_31374chr1:10781495-10788546Gastric
SE_40607chr1:10772324-10790002Left_Ventricle
SE_41555chr1:10781532-10785534LNCaP
SE_41555chr1:10785643-10788541LNCaP
SE_42099chr1:10779231-10788633Lung
SE_47486chr1:10783767-10784248Pancreas
SE_47486chr1:10784380-10785439Pancreas
SE_47486chr1:10785707-10786041Pancreas
SE_47486chr1:10786176-10787914Pancreas
SE_48119chr1:10782759-10788636Psoas_Muscle
SE_48591chr1:10773352-10788686Right_Atrium
SE_49447chr1:10781476-10784257Right_Ventricle
SE_49447chr1:10784422-10785425Right_Ventricle
SE_49447chr1:10785569-10788365Right_Ventricle
SE_54510chr1:10783384-10788141Stomach_Smooth_Muscle
SE_65281chr1:10783274-10785800Pancreatic_islets
SE_65281chr1:10786062-10788457Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11078402810784719
Number: 1             
IDChromosomeStartEnd
GH01I010722chr11078291210789847
Enhancer Sequence
CATTAAAACC ACCCATAAAA CAGAGGAGCC ACTGGCTGTG GCTCTGAGCA GTCTATTCAA 60
GCCAGGCGCC AGCCTCTCAC CTGCTGCCTC ACCCCTGCCC CGGTGCCCAG CCTGGGGGCA 120
GCACATGCCC TGTTGGACAC GGCAAATTTG GGTGGGGTTA GGCCAGCTTC CTGGCACTGG 180
GCAATGGGGT CCTGCGCTTT GCAGGTGCCT TTCTCATGGC TTAGAGGAAA GGACCCTCCA 240
GGGCATCAAA TCAGCAGCCC TGGCTGGAAG CTGCCCCCAT CTCTGAATCT TCCTTGGCCC 300
TGTCTCCCAC TCTCTTTTCT CCATGGCCTG GGTCCTTCAG GACTAGATGC CCAGGAAGCT 360
CATCCAGCGG TCACATTTCC CTCTAACTCC CCCTGCAACC TGGCTGCTCT CACGGTCAGC 420
TTCAGTCCAC CCGTCTCAGG TGGCCTCCCC AGTTCAGCAC TGCCTGGGTC ATGTGCCCCA 480
GCCCCAGAGC CCACCTTCTC CTCTTCTTTG GGGGTTCTTC CCGAGTCCAA ACCATGCCAG 540
CAGGGGTTCA ACCCTAAACT CACACCCAAC CGCTAGCACC TGCCCCAGCC TCCCATATCA 600
CTTTGGATTC CTGGTGAGGA CAAGTCCAGT TTTCCAAACC GACCTTGGAG CTCTTTGACC 660
ACAGCACACT TTGGGAGAAG GTGGAAGAGT CCTCCCCATC TTTGCCAAAA GAGGTGTCAG 720
GCTAACGTTA CACCAGCTTT AAAAATACCC CAGCACACGA TCCACAGGGT GAGAGCAAAG 780
GCCACGTGGT CAGAGCCGGG CTATAAATAG CCAGCAAATC ATTTCCCAGA GCCACGGCCC 840
CCTCCCCAGC ACCAAGAACC TTTCTGAGGA AATCAAAGTG AACGCAACTG TTACCAAGTC 900
ACTACTAAAA TATTTACCAG CCTGGCGAAG TGCCGAAGGT GCTTGGCACC GAGTGTTTGC 960
TTATTTACAA GGCTGTTTTA AAGGGTAGAA AGCAAAATAA GGTAACCTGA GCTATTAAAC 1020
CCGGGGGCCA GGTGGTACCT ACCAGCTGTC AGCCACCCCA GGCATGTCGG GAGCTAGAAC 1080
AGTCCTGGTG GAGATTCCCT TGAAATGGGT CAGGAAAGCA GAGAGAGGCT TTGGAGCCCA 1140
GGAATCACCT AGCCCTCAGG GGTAGGGGCT CAGGGAGTGG GAGCAGAGAG TGTTAGAGGT 1200
TAGAGAAGCA CTTCTCCCCC AGCCAAAGCA AGCAGGGCCT AGCACGAGCT CCAAGGTTGC 1260
CCCTGGTCTT CGCTCAGAGG GGCACCCCAA GGGCACTGCC CAGCCAGAGG CAGGGGCAAG 1320
GGCCCTGGGA GGGAGAGGCA AGGCGGGGAA GAGGAGGCAG AGGAAGGCAG GTGGGGGGCT 1380
GGCTGGGAGC CTCGGAGGAT GACATAAGGG GGACACAGCC AACCTGGGGA AGAGAAGGTG 1440
CTCAACTTCT CTCTTTCTCC TCTTTCTCTG AAGTTTCCTT GTGGTTTGAA TTTAATTTTG 1500
ATTTTCTCAA CTTCAGCAGA TTGAAGTTGA AATAACCTAC AAATTACTTA ATGTGTTGTA 1560
AATCTGGGGG AATTCAGGAG TAATTGGGAC CACATGTTGG CCGGGAGGGA GCCCACAGAG 1620
GACGGAGGGA AGCAGCCCTC GCAGACGTGC AGGTGGCTGT TCTTCCCTGG AGGGAGGGGG 1680
CTTGGGCTCC CCTCGGTGGG GGTAGGATTC CCTAGTTGGC CAGGGAGCCC TGGATGGATA 1740
CGGCGAGAAC GTGTTAAGAC CAAGGAGTGA CCATGTCACT GCCCAGGGCA GCCCGGTGAC 1800
CGTGGACACA GGGCGGCCAA GTAGGCTGGG TGCCAGGCGT CTGCCAGGCC CCTCCACCGT 1860
GCCAATGCCA ACACCGTGGC CGCCTCCCGC TGCATGCGTG TGGCTGTCAG CTGAGCTCCC 1920
CTCCCGCCCT CCCTCTCCGG CAGGCTCCTC TCAAGTACTG AGCCATATGG TTCCAGTTAA 1980
GCTCCATATT TTTCCTTGTC GATTGAAGAG ACACACTTTC CTCTTTGCCA GACAGTTTGC 2040
AGATTGCTCT GTTGGCTCAA TTTCTTATTG GATTTCTCAA AAAACCTGAC ATTTTAAATT 2100
AATTTACAGC CACAACAAAA AGAGTTCAGA ATTTTAATGG TGTTGTAAGT AATTTTTAGG 2160
TAATCCACTC CAGATTTTGA TATTAACCTT TGAAACTGGA GTTCATTCAG CTACCATGTT 2220
ACAATCCAGT CACACTCCAG GCCTGGGGGA GGCCAGGCTT GGGGAGGAGG TGGAAGCCAG 2280
GTTCTGGAAA GCCCTTTTTT TTTTTTTACT AGGAGACCCC AGAGAGGATG ATCCTGGGGA 2340
ACCCTGGACA GGTGAGTGAC AAGACAGCGG CAGTGGGGTG GGGAGGGAAT GGCAAGGGGG 2400
GCCTGAAGAC AGCAGGGCAG GTGTAAGAGA GTCATTGAGG GGGCCAGAGG GCCTGCCGAA 2460
TGTTCTAGAA GGATGGGCCG GACTTAGGAG GGGGCAGCAT CCTCAGGATC CCTTAGTAGC 2520
AAGAGCAGGG TGAGGCTCCA CCTCAGTGCA CTAGGAAATA ATGGTAATAG CAATAATAAT 2580
GACAGCTAGC ATTTGCTGAG CAGTCACTAT CTGTCAGGGG CTGTACCATC TCATTGATGC 2640
CTCCAACCAC CTATGGGGCA GGGCCTATAC TATCACCACC ACCACTACTA CCAGTACTAC 2700
TACTACTGCT GCTACTACCA CCAGCATGAC CATTAATTGT TAGTGTTTAT GGAGGGCTGA 2760
CCGCGTCCCA GGCAGAGTGA AGTCGGTTTT ATAAACCACC TCATTAAACA GCAACAGAAA 2820
CCCTGTAGGA GACACCACTG TTCATGCCCT CATTTACGGA GGAGGAAATG AGGCTTGGGG 2880
AGGTGAAACC GGGTCTCCCC AGCTTGGGGC TACTGACCAA CAGCCACGCT CTGGGATGCC 2940
GCCATCCTCA GCCTACTCCG TATCTCCTTT CAGAAGATGC TATGAAATAC TCATGGCCAT 3000
CACAGTCCTC CTGGCTGGAG CCGGAGGGAG GAGGAGGGCG GTGTAGTCCT CCAGGCTGGC 3060
CAGGCTGGGG CCGGTGGAGG ATGCCACCTT TTCCTCGTGC CGCCTCAGGC CAAGCTGAAG 3120
GCTGCATGCC AATCCGGCCA GAGGAAACAC CGGGCACGGG GAATGGAGCC CTCGCCAGCG 3180
TCTTTACTAG GCCCTGGCGC TGTGCGGCCC CTGCCTGGGT GCGGTGCCAG CTCACTACAC 3240
CAGCAGATCG TTAGCATTCC TTTCCTGCAG GAGCTGCCCA 3280