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

TagContent
EnhancerAtlas ID
HS041-02763 
Organism
Homo sapiens 
Tissue/cell
EWS502 
Coordinate
chr1:230245040-230245890 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr1:230245358-230245373GAGGTCAGAAGTTCA+6.38
RARAMA0729.1chr1:230245358-230245376GAGGTCAGAAGTTCAAGA+6.88
Number of super-enhancer constituents: 13             
IDCoordinateTissue/cell
SE_25348chr1:230236453-230250730DND41
SE_31112chr1:230238334-230250198Fetal_Thymus
SE_34791chr1:230245338-230246545HeLa
SE_39366chr1:230243332-230245406Jurkat
SE_39366chr1:230245502-230246254Jurkat
SE_43672chr1:230244327-230246934MM1S
SE_49908chr1:230243259-230245387RPMI-8402
SE_50426chr1:230243483-230247391Sigmoid_Colon
SE_58501chr1:230239434-230311477Ly1
SE_61418chr1:230219055-230306985Toledo
SE_65792chr1:230244744-230245625Pancreatic_islets
SE_66256chr1:230243332-230245406Jurkat
SE_66256chr1:230245502-230246254Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1230245250230245310
Number: 1             
IDChromosomeStartEnd
GH01I230109chr1230244801230246713
Enhancer Sequence
GTGGTGGTTG GGGGCCCTGC AGGCTCCCTC GGGGTGTAGC AGGGACATGG TGTGGTGGTT 60
AACAGGAGTA GGCCACTCAT GTGGGACGTC AGGACTAGTG CCACAAAGGC AGCCCTGTCA 120
CACGAACAGG TTCTTGGGGG ACAGAGGTCT GTCTGGGACT GGCTAATGAC CTGGAAAGAC 180
TGGAGAGGCA CCATTGTCCA CCACCAGATG TATGGCTGCA GGGTAGGAGT AGACTTAAGA 240
AGGAACACTG TTGGCTGGGC GCAGTGGCTC ACGCATGTAA TCCCAGCACT TCGGGAGGCC 300
GAGGCAGGTG GATCACCTGA GGTCAGAAGT TCAAGAACAG CCTGGTCAAC ATGGTGAAAC 360
CCCATCTCTA CTAAATATAC AAAAATTAGC TGGGCGTGGT GGCAGGTGCC TGTAATCCCA 420
GCTACTCTGG AGGCTGAGGC AGAAGAATCA CTTGAACCTG GGAGGCGGAG GTCGCAGTGA 480
GTTGAGAGAT CACGCCATTG CCCTCCAGCC TGGGCAACAA GAGCGAAACT TCGTCTCCAA 540
AAAAAAAAAA AAGAAGGAAC ACTGTTAGGG AGGCAGTCAG TGAGCCTCAA GTCAGAAAGA 600
CAAACAAGCT CATTTTATGC ATTTGCTAAC ATTTGACCTC TTCTGGGACG CGTAGGTCTC 660
TCAAGTTCTG TTTCTGTTTC CTGTCACGCA GATCAGAGAT GTGAAACAGA CCTGGTGTAC 720
ACCCGTCTGG GGTAGCACTG GGAGCCACGG CGTCCTGGCA GAGCAGGTGT GCCTCCCACA 780
GGCTGATGCA GCCGTTCTCT GTGCAGAGGC TGAGCCATCC TAGGAGCAGC TGTGGGGTGA 840
AAGTGTCCTT 850