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

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EnhancerAtlas ID
HS139-22026 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr17:1480360-1481540 
Target genes
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr17:1481439-1481454GGGACAGGCTGACCC-6.32
SPI1MA0080.4chr17:1481159-1481173AACTTCCGCATTTA-6.42
SPIBMA0081.2chr17:1481159-1481171AACTTCCGCATT-6.27
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_09501chr17:1477198-1482172CD14
SE_24303chr17:1480428-1481001Colon_Crypt_2
SE_24303chr17:1481005-1481629Colon_Crypt_2
SE_25267chr17:1480380-1481766Colon_Crypt_3
SE_27390chr17:1480364-1481857Esophagus
SE_41871chr17:1480390-1481757LNCaP
SE_50860chr17:1480343-1481848Sigmoid_Colon
SE_53184chr17:1480354-1481865Small_Intestine
SE_68949chr17:1480336-1481912H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1714804001481470
Number: 1             
IDChromosomeStartEnd
GH17I001573chr1714771521482396
Enhancer Sequence
CGTTGGCCAG GCTGGTCTCA AACTCCTGAC CTTGTGATCT GCCTGCCTCG GCCTCCCAAA 60
GTTCTGGGAT TACAGGCGTG AGCCACCGCG CCCGGCCCTG CTGGGTGGTT CTGCAAAGTG 120
TTTCTCTTTG GACCAGCTCC AGGCCCCAGA CTCTGGGGAG GGCCCACCCC ACTCAGCTGT 180
GCCCAGGGCC TGTGGGTGTC TGGCTGAGCC GAGTGGAAAG CGTGGTGCCA GCGGGGACCT 240
GCGGTTTGGG AAACAGGCCC AGAGAGGAGT GTGGAGGCTG GGCTTGGCTC TGCAGTGCCC 300
TCGTCCAGAG AAGCATTGAG TAATCGCGGA AACTCAGCAC CACAGATCCC GCCCCCCTCC 360
CTCAGACCCT GCCAGGACAG CCACAGCTTC CTCCAGGCCT GGGGAGGGGC AGGCGGAGGG 420
CAAGCGGAGC TGGGATTACC CCAGGGGCTG TTGCGGGAAT TGGGAGAGAG TTCCGGGCTA 480
AATCTTAGCA CATGTCAGGC TCTGCTGGCC CAGAGGTGGG AAAGGAATCC CAGCAACACA 540
TGAGCTGGTC CCACATCAGA GACTGTGGAT GATGATGTTT GAGTTTCAGT TTTTGGGTCA 600
AGGCCTGAGC CAGAGAAGAA GGAACCACTG TGGTTCCTTT TATGTTTCTG GGGCTTCTTG 660
GAAAAAGATA CAGGTTTCAT TTTAGCCAGG GCTGGAGAAA GCTATGGCCA GAGCTGGGCG 720
CACTGAGGCT CTGGATGGGC CCGTCTGGTG TATTCTGGAC TCAGTCACCC ATGTTGCTGC 780
CCGTGATGAG GGCAACTGGA ACTTCCGCAT TTAGCTTCAG GCAGCCAGAA CCTACCCATC 840
CTTCCCAGTG AGCAGCCAGG GCCAGCCCCA GGACTCGGCT GTAGTGGCCC CTGAGGCCAT 900
AATGAGCTGC ACAGGTGCCT GACCCTGGCT GGGGGAACTG ACTTCGTGTT GAATGCCAAG 960
GCTTGTGAGC ACCCAACTGT CTGCCCACTG ACCTGCTTCC CACGAGGTAT GGCCTTTCCC 1020
TGAAACACCC AGCAGAAACC CTGGTACCTG TCCCCTGAAG CAGGAAGATG AGCCCTTCTG 1080
GGACAGGCTG ACCCTGCCTC AGAGTCTCAG TCCCACCAGC AACCTCCCCC CGGCCATTCC 1140
CACACCCTCG CCCACCAGGC CACCTGCGGC TTCCAGGACT 1180