EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS042-00634 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr1:15531280-15534510 
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:15532831-15532849GGGAAGAAGGAAGGAGGG+7.09
EWSR1-FLI1MA0149.1chr1:15532851-15532869GGAAGGAGGGAGGGTAGG+7.13
EWSR1-FLI1MA0149.1chr1:15532835-15532853AGAAGGAAGGAGGGAAGG+7.68
EWSR1-FLI1MA0149.1chr1:15532847-15532865GGAAGGAAGGAGGGAGGG+7.97
EWSR1-FLI1MA0149.1chr1:15532843-15532861GGAGGGAAGGAAGGAGGG+8.34
EWSR1-FLI1MA0149.1chr1:15532839-15532857GGAAGGAGGGAAGGAAGG+9.93
RELAMA0107.1chr1:15534435-15534445GGGAATTTCC+6.02
ZBTB18MA0698.1chr1:15534009-15534022AATCCAGATGTGC+6.62
ZNF263MA0528.1chr1:15532848-15532869GAAGGAAGGAGGGAGGGTAGG+6.19
ZNF263MA0528.1chr1:15532844-15532865GAGGGAAGGAAGGAGGGAGGG+6.25
ZNF263MA0528.1chr1:15532856-15532877GAGGGAGGGTAGGGAGGGAAA+6.49
ZNF263MA0528.1chr1:15532766-15532787AGGGGAGGGGAGGGAAGGGAA+6.71
ZNF263MA0528.1chr1:15531997-15532018TCCTTCTCCCTGCCCTCCTCA-6.86
ZNF263MA0528.1chr1:15532833-15532854GAAGAAGGAAGGAGGGAAGGA+6.9
ZNF263MA0528.1chr1:15532758-15532779GGAAGAGGAGGGGAGGGGAGG+7.17
ZNF263MA0528.1chr1:15532761-15532782AGAGGAGGGGAGGGGAGGGAA+7.18
ZNF263MA0528.1chr1:15532852-15532873GAAGGAGGGAGGGTAGGGAGG+7.28
ZNF263MA0528.1chr1:15532836-15532857GAAGGAAGGAGGGAAGGAAGG+7.58
ZNF263MA0528.1chr1:15532840-15532861GAAGGAGGGAAGGAAGGAGGG+8.5
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_31469chr1:15527874-15531661Gastric
SE_31469chr1:15531669-15532253Gastric
SE_31469chr1:15532359-15535771Gastric
SE_47623chr1:15532961-15534364Pancreas
SE_54674chr1:15526004-15535129Stomach_Smooth_Muscle
SE_65327chr1:15530341-15531919Pancreatic_islets
SE_65327chr1:15532220-15535190Pancreatic_islets
SE_69144chr1:15532523-15534592H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr11553176015531892
chr11553278515532847
chr11553299415533890
Number: 2             
IDChromosomeStartEnd
GH01I015205chr11553246415534799
GH01I015206chr11553167015532253
Enhancer Sequence
GTAAAGTGCC TGGGGTGTCA GTGCCCTAAC TATGTGCTGG GGGTTGGGGG ACTAGAGTAC 60
TGGGGGTCTG GCTGATGGTC AGAGCCTGTG CTTAGCCTTG TTTGCCAGGG TCGGGGGGCT 120
GCTGCTGTTG TCCCCAGAGA CACCGATGGC CAGAACCTGG AGAAGGTTCG AGGTGTCAGA 180
CTCACATTGG GCTGACGGGG ACAGGAGATC TGCATCCCTC AGTGCTATCC TGGCAGAGGA 240
AGTCTCTGAA ATGTGAGATG TCACATTTCC CAAGAAATAC TGAATGTGAC TGGGTCCCCC 300
GTGCCAGCCT TCTAAATAAG GCTGGACACC AGCCACCTGC TTAGAGAAAG ACACTATGTC 360
AAGTGCCTCA AGAAAAGATG TATGGTTCAT GAACTCGCTG CTTCTGCTTC TGGTCCCTTG 420
AGTCTTCAAG ATGAACTTGT CTTCCTTAAT TTCTCCAACA CTTACGTGGA TTAGCAAGGA 480
CCCTGGTGAT GTCAGGTTTT ATACAATGCA CCGACAGCTT GTGTTTGGAG TCGGGGAGGG 540
AAGCTGCCTC TTTTCTCTGC AAGCCATGAC ATATTCTGGA AGATGCCCAC TTTCCCATCG 600
CTGTGGGATT ACTGAGGCTG AGCCCTCACC CTGGAATATC CTGATCTCTT ACCCCCAAAT 660
TCCACCCACA GGAAGGCCAC AGAGGCCTCA AGGCCCTGCA GAGCTGCATG CGTATCTTCC 720
TTCTCCCTGC CCTCCTCAAA TTGAATCCGT CATTCTTTTT GGAAGCTCTT CAGACACGCT 780
CCATTTTGGC AGTGCTACTT GGTGTTTAAA AGTGTGGGTT TTAGGATCAG GCGTACCCTA 840
CCCCTGCCTC GTACTCACTG TGTGACCTTA GAAAAATTAC TTTCCGTCTT GGAACCTGTG 900
TCCTTATCTA TAAAATAGAA CCAATAACTA TTAAATGATG ATGCACATAA AGAGCTCCAC 960
AGAGGGCCTG GCACAGAATT GGCATTCAAC ACACATTGAT GCTTTCTCTG ACGCTGACTT 1020
CCCTTCTGTT AGGCAGAATC GCCTGTCTTC CTGCTGGATT GTAAAAGTCT GTCTCATGTA 1080
TCTCGGTATC CCCCAAAGCT CCTGGCATAC AGTAGGGGAA CCGGGAATTG TTTAAATCAA 1140
AATCTTCAAC AAGTCATTTT AAAAGAAATG TTCAGGTCCA GTAGCTCATG CCTGGTAATC 1200
CCAGCACTTT GGGAGGCTGA GGCAGGCAGA TTGCTTGAGC CCAGGAAATC GAGACCAGCC 1260
TGGGCAACAG AGCGAGACCC TTTCTCTACA AAAGACGCAA AAAATAGCTG GACATGGTGG 1320
TGTGTGCCTG TAGTCCCAGC TCCTCGGGGG CCGAGGTGGG AGGATTGCTT AAGCCTGGGA 1380
GGTCAAGGGT ACAGTAAGCC ATGATCATGC CACTGCAGCC TGGATGACAG AGTGAGACCC 1440
TGTCAAAAAA AAAAAAAAAA AAGAGAGAGA GAAGAAAGGG AAGAGGAGGG GAGGGGAGGG 1500
AAGGGAACAT TTACCTGTCA CCCCCTCACA CTTTTGTCCT GAAACACCTC TGGGAAGAAG 1560
GAAGGAGGGA AGGAAGGAGG GAGGGTAGGG AGGGAAACAT TTACCTGTCA CCCTCACACT 1620
TTTGTCCTGA AACACCTCTG GGAACCTCGG TGCCTTGCCC AGAAAGTGGC CCCCAGGGAC 1680
TCAGCTTTGT GGGAACCCGC ATAGTGCAGG CACAGGTGGA CTTCACAGTC AGCTGGATTT 1740
GATTATGAGT CGACTGTGCC ACTTACCGGC TGTGTGGCCC AGGGCAAATT ACTTACCCTG 1800
TCCAAGACTC CAAGATGGTG GGGCAGATCA TTCCTTGAAG GGTGGCCGTG AGGATCGGGT 1860
GAGTTTAGGA ATGCACCTGA TTCATGCTGA GTATCAGCTG CTGCTGATTT CATGATAGCT 1920
GCTGCGGAGA CTGCTATTCT TGTTACCATT ATTCTTCTTA CCCTGCCTTG TGTATTACTT 1980
AACATCCTTT CTTCTTTTTC CCATCAGCTC TCTCCAGCTG GGCAGCCCTC CTCCCAGCTC 2040
CCCTGCCTCT ATGCCTCATT TGCACATTGC TTTTTGTTTT TCCCTAGTGC ACAGTCTAAA 2100
AGATCCCTGG TGCTCTGTTG AAACAGGAAC CTGACACCCT TTGACCTTGG TCCGTGGGGA 2160
GGTAGCCTGA AACTCCCTCC CAGGCAGGAC AGGAGCAGGG GCTCAGCACC TTTTTTCCTA 2220
CCCCCACTGC ATGGGACTGG AAATTGTGAC AAAAGTGATT GTGGGCTGAA ACTTGGCAGA 2280
GAGAGCCCCA CTGAATTCCT CCTTTGTGAT GTGAATGTGG CACAGCCCGG TGGAACCGGG 2340
GATCCCTTTC CCAATTATGC AGCTTGGCAG GAAGAGGTCG GTGCAGGGAG AATGCTCAAG 2400
GAGCCCCTCT GTCATGGGGG TTGGTAGCAC CGCCAGCCGC CTCCGACTGG CAAGACCTCC 2460
TCCCACTAAA GCCAGCTGGG CTGGGCGCTT CTGCAACTGC ACCTTCCGGG GCCACAGCAC 2520
AGAACTCAGT GGTCACGTGA GGGTCTACAT CCGATTCCCA GTTTCTAAAC TGTGTCCTGG 2580
AGAGTTTCTG CAATTCAGCG AGAAGAGGCA GCGGAAGGCC CAGCCATCAA TGCTTGGGCC 2640
CTTTACCCCG TTTCAGCCGG GGCAGCGCTG CTTTCCATCG TCCCATCTTA TTTCAGTCGT 2700
TGTCTTCACG TTCAAGTTCA TGGAGACTCA ATCCAGATGT GCCTGGCTGT GATGGCCCCA 2760
CTCAGGTCTC AGCCACTCTG ATGTCTGGAG CTGGGTCTAC CTCCCTGGCC CCGACTCCTC 2820
CACACCCACT GCACAGCCCC TCCCTGCCGG CTCTGGTTGG CCAGGGGTGT GCACACGAGT 2880
GGAAAGAGCC TCTGCCCAGC GTGGAGCGGT GAGGCTAAAG GCTTCCATGT TCCCTGCTGA 2940
CTTCCACCTG CAAAGGCCAG GCAACCGCTG AAACCTCCAG CCCCACCAGG GAATACTGAT 3000
ACAGTCACTT TCTCAGGTCA CAACGGAAAT CACATTTATT CTGCATATTT TCCTCATGTT 3060
GCCGGCAAAT TATTTGCATA CGGATACAAG ATTTGGGTAT CTGGATCTTC CTGCAAGTTA 3120
GCTTTTATTA ATCCTCTCCC CTTCAGGCTT GGACTGGGAA TTTCCCCTCA TTGATATGAG 3180
ACATTGGTTC AACTTTTAAA CTTGCCAGGT ATTCATTTGT TTGTTCTATA 3230