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

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EnhancerAtlas ID
HS120-03603 
Organism
Homo sapiens 
Tissue/cell
LNCaP-abl 
Coordinate
chr2:20407740-20408690 
Target genes
Number: 9             
NameEnsembl ID
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxo1MA0480.1chr2:20408102-20408113TCTTGTTTACA+6.02
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_02914chr2:20407353-20409539Bladder
SE_23108chr2:20407449-20409559Colon_Crypt_1
SE_23761chr2:20407582-20408957Colon_Crypt_2
SE_24805chr2:20407649-20408942Colon_Crypt_3
SE_26530chr2:20403978-20426236Esophagus
SE_28384chr2:20407358-20409558Fetal_Intestine
SE_29057chr2:20406148-20409772Fetal_Intestine_Large
SE_31478chr2:20407303-20419416Gastric
SE_33954chr2:20407406-20409301HCC1954
SE_35878chr2:20404964-20426386HMEC
SE_41823chr2:20404831-20409818LNCaP
SE_42432chr2:20403633-20409872Lung
SE_43614chr2:20404132-20426415MM1S
SE_50296chr2:20404815-20409905Sigmoid_Colon
SE_52465chr2:20407277-20409713Small_Intestine
SE_64257chr2:20407485-20409929NHEK
SE_67169chr2:20404132-20426415MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr22040788320408194
Enhancer Sequence
CACCGCCTCC CCCAAGAGAA AGCTCAAGAT GGGGCAGGGA TGGGGCAAGG CACTGGCACT 60
TCGACCCCAC GAGCCTCTGC TGCATTGTAG AGTGCCGAAT CTTTCAGCAG AAGCTAGAAC 120
CATTGGATCC ATGCTCCATT CAACAATGAG GCAACCGAAG CCCACAGGGA AGACACACAC 180
ACTGGGGCCC ATGTACAACC TGGGAGACAC CGCCCAGTGA GACCCAGGAA CGCCAGGGAG 240
GCCCCAACAC GTTAGCAGTT TCCCAAGAGC AGGGCTTTCC TCCTGACTAG ATAAGCATTT 300
CAGTCTGCCC TGTCCCTAAA AACAATTTGT TCCCTCAGTT CGGCTGGCTT ATCCCTCTGC 360
AATCTTGTTT ACACAACAAG CTCTTAAGCA AATGTTTTCT CCACTGAAAC CAGCTCCCTG 420
GCCTCCGGGG GCCTCTCCCC TCCCTGGGCC TTCAGTCTCC ACTAAGGGGA CAGGCTAGAG 480
AGACCTCCCA AATCTTCTCC AGCTTGAATC TTCTGGGACA GCCCCTCAGA TGAGAAGGTG 540
AGATTTCAGC CCCCTGAGGA GGAAATTAGC AGAAACTGCT GAGTTTGAAC TTGGATTACC 600
AAGGTGCCAG CTGACTCCCG GAGTTTCTGG TGAGACTTTC GATTTCCTTT AGCAGGCCTG 660
CTGTGCTGAC AGCCGGCAGC AAACTCCCTC TAGGCCTCCT GGGTAGCTCT CCCCAGCATC 720
ATCTCCAACC TGGGTGCTTC CGAGGCTGCC TGGCCACGGC TCAAGGCTGC TCAGGAACAG 780
GTGGCCTCAG CTTGGAGACT ACCTAATGCC CTGCCCAGGA AGGCAACAGG CTAACCAGCC 840
TTTAACCTCT GTAAGTCCCA GGAAAACCAA CTGTTCATAG AACGAATCAA CAACTTTGTG 900
CTAGGTAAGA TCTAGGCTTC CACTCATTCT GTTGTTCAAA GCAAGGGATG 950