EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-17594 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr2:238569080-238569660 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EHFMA0598.2chr2:238569203-238569215AACCCGGAAGTT+6.44
ELF1MA0473.2chr2:238569203-238569215AACCCGGAAGTT+6.52
ELF3MA0640.1chr2:238569203-238569216AACCCGGAAGTTC+6.02
ELF4MA0641.1chr2:238569203-238569215AACCCGGAAGTT+6.44
ELF5MA0136.2chr2:238569204-238569215ACCCGGAAGTT+6.14
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_01566chr2:238568879-238571154Aorta
SE_23331chr2:238568885-238570238Colon_Crypt_1
SE_23963chr2:238569256-238570053Colon_Crypt_2
SE_24998chr2:238569122-238570436Colon_Crypt_3
SE_31908chr2:238568844-238571159Gastric
SE_42111chr2:238568829-238571135Lung
SE_48071chr2:238568749-238573479Psoas_Muscle
SE_51094chr2:238569466-238573270Skeletal_Muscle
SE_58523chr2:238563966-238621920Ly1
SE_65656chr2:238569477-238570566Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2238569179238569490
Number: 1             
IDChromosomeStartEnd
GH02I237660chr2238568862238573173
Enhancer Sequence
GCTGGCCAGT GTAGGTTTGG GGACATAGGG ACCCCCACAG TGCTGATGAG AGAGTCCACA 60
GCAGCTATCT CTGCAGAGTA CAGCTGGCCA GCATCTGTCC ACTTCAAAAG GCACATGCTG 120
TTTAACCCGG AAGTTCTACC TCTGGGAATT TATCTTGCAC CTCTACTCCC ATGATATGAA 180
ATTCCAAGTC ATTTGCTGCA GTCTTGCTTG TAGCAGAAAA ATGTGGAAAC AAACAAATTT 240
GTCTGCCATA AAGGACTGGT CAAACCTGTT GCCATCCATA CAAGGAGTGC CACGAGCTCC 300
TGTGCACCTG TGGAAGGAGC TCTGAGCTAG ATTGTTTAGC AAGAAAAGCT TCAACACACA 360
AGTTCAGTGA AAAAAGCAAG GGCAGAACAG CGCACGGTGC TACATGTCTG TGGCAGAAAA 420
AGGGAGAAAA GCATGCGTTT TTGAGTTTAT ATATTCCATC ACCTTCAATA TACAGCGTCG 480
GGACACCTGA CCACCTGCAG GACCCACTGT CATCCTGGGA GAGGGAGGAG GAAGCTCTCG 540
GATCTCCTCT TGTGAAAGAG GCGAGATTAT TGCTCAGCCT 580