EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS139-26057 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr19:10055860-10056800 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs80076900chr1910056320hg19
TF binding sites/motifs
Number: 32             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:10055907-10055925GGAAGGAAGGAAGGAAAG+10.53
EWSR1-FLI1MA0149.1chr19:10055895-10055913GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:10055899-10055917GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:10055903-10055921GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:10055883-10055901GGAGGGAGGGAGGGAAGG+6.94
EWSR1-FLI1MA0149.1chr19:10055878-10055896GGAAGGGAGGGAGGGAGG+7.08
EWSR1-FLI1MA0149.1chr19:10055911-10055929GGAAGGAAGGAAAGAGAG+7.37
EWSR1-FLI1MA0149.1chr19:10055874-10055892GGAAGGAAGGGAGGGAGG+8.13
EWSR1-FLI1MA0149.1chr19:10055887-10055905GGAGGGAGGGAAGGAAGG+8.45
EWSR1-FLI1MA0149.1chr19:10055866-10055884AGAAGGAAGGAAGGAAGG+9.09
EWSR1-FLI1MA0149.1chr19:10055870-10055888GGAAGGAAGGAAGGGAGG+9.42
EWSR1-FLI1MA0149.1chr19:10055862-10055880GGAAAGAAGGAAGGAAGG+9.47
EWSR1-FLI1MA0149.1chr19:10055891-10055909GGAGGGAAGGAAGGAAGG+9.47
FOSL2MA0478.1chr19:10056311-10056322GGATGACTCAG+6.32
IRF1MA0050.2chr19:10056624-10056645TCTTTCTTTCTTTTTTTTTTT+6.25
JUN(var.2)MA0489.1chr19:10056308-10056322AGAGGATGACTCAG+6.25
JUNBMA0490.1chr19:10056311-10056322GGATGACTCAG+6.14
ZNF263MA0528.1chr19:10055912-10055933GAAGGAAGGAAAGAGAGAGAG+6.03
ZNF263MA0528.1chr19:10055892-10055913GAGGGAAGGAAGGAAGGAAGG+6.24
ZNF263MA0528.1chr19:10055908-10055929GAAGGAAGGAAGGAAAGAGAG+6.28
ZNF263MA0528.1chr19:10055904-10055925GAAGGAAGGAAGGAAGGAAAG+6.48
ZNF263MA0528.1chr19:10055867-10055888GAAGGAAGGAAGGAAGGGAGG+6.76
ZNF263MA0528.1chr19:10055880-10055901AAGGGAGGGAGGGAGGGAAGG+6.76
ZNF263MA0528.1chr19:10055896-10055917GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:10055900-10055921GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:10055871-10055892GAAGGAAGGAAGGGAGGGAGG+7.19
ZNF263MA0528.1chr19:10055888-10055909GAGGGAGGGAAGGAAGGAAGG+7.27
ZNF263MA0528.1chr19:10055875-10055896GAAGGAAGGGAGGGAGGGAGG+7.38
ZNF263MA0528.1chr19:10056339-10056360GGAGGAGGGAAGGGGGAGGAG+7.59
ZNF263MA0528.1chr19:10056333-10056354GGGGGAGGAGGAGGGAAGGGG+7.83
ZNF263MA0528.1chr19:10055884-10055905GAGGGAGGGAGGGAAGGAAGG+7.95
ZNF263MA0528.1chr19:10056336-10056357GGAGGAGGAGGGAAGGGGGAG+8.62
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr191005623610056512
chr191005600610056600
chr191005593710056626
Number: 1             
IDChromosomeStartEnd
GH19I009944chr191005525710057156
Enhancer Sequence
AAGGAAAGAA GGAAGGAAGG AAGGGAGGGA GGGAGGGAAG GAAGGAAGGA AGGAAGGAAG 60
GAAAGAGAGA GAGAGAAAGA AAATAGACAC ACACACAACT CCACAAAACC CACAATTCAG 120
ACACACAGCT CACACACAGG TCTCCAGCAT AGACATATTT ATACATCCGT TTACTCAAAC 180
ACTCACAATA CAATCACATA AAACAGGCAG ACAGTTCACA TGCCAACACA CTCTTGCACA 240
GACACGCAAA CAGAAGCATG GAATTTGTAC AGAGCACGCT CACAGTGTCT GATCCATAAC 300
TCAGACACGG AGTCACGCCC ACAAAGGCAC AGTAGAGGCA GAGTTCACAC ACAAACAGAC 360
CCGCGGGGAC CCACGACACA GCCCTCTGAC ACGAGGACGC CAGGCCAGGG CAGCGTGGGA 420
ATGAGGCTGC AAGGAGGGAG TGAGGTGGAG AGGATGACTC AGGAGGCCTC TCTGGGGGAG 480
GAGGAGGGAA GGGGGAGGAG GGCAGGCATC CAGCGCATGT GGTTCCTATT AGGGGCCTGG 540
GAATTGAGGC ATGAGCTGGC GGGACAAGGA GACCCAGGAA CGCTTCCCAG CCTTACCAAA 600
GCAGGAAGGA GCAGGGCCCT GATCTAAGGC CATGCGGCCG GAACTTGGCT CAGAACCACA 660
GCCGTTCTAA GGCAGAGTGG TCTGCCCCAA GCCAGGCCCA GCAGGGGGCT CATTTCAACC 720
CCTGCGATAG TCCTGGAGAA GATTTCTTTT TATTTTTTCT TCTTTCTTTC TTTCTTTTTT 780
TTTTTTTTCT GAGACAGAGT TTCGCTCTTG TTGCCCAGGC TGCAGTGCAA TGGCGCGATC 840
TCAGCTCACT GGAACCTCCA CCTCCCAGGT TCAAGCGATT CTCCTGCCTC AGCTACCCGA 900
GTAGCTGGGA TTACAGGCTC CTGCCACATG CCTGGCTAAT 940