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

TagContent
EnhancerAtlas ID
HS184-16003 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr2:20407730-20408670 
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
TCTCCTGCTG CACCGCCTCC CCCAAGAGAA AGCTCAAGAT GGGGCAGGGA TGGGGCAAGG 60
CACTGGCACT TCGACCCCAC GAGCCTCTGC TGCATTGTAG AGTGCCGAAT CTTTCAGCAG 120
AAGCTAGAAC CATTGGATCC ATGCTCCATT CAACAATGAG GCAACCGAAG CCCACAGGGA 180
AGACACACAC ACTGGGGCCC ATGTACAACC TGGGAGACAC CGCCCAGTGA GACCCAGGAA 240
CGCCAGGGAG GCCCCAACAC GTTAGCAGTT TCCCAAGAGC AGGGCTTTCC TCCTGACTAG 300
ATAAGCATTT CAGTCTGCCC TGTCCCTAAA AACAATTTGT TCCCTCAGTT CGGCTGGCTT 360
ATCCCTCTGC AATCTTGTTT ACACAACAAG CTCTTAAGCA AATGTTTTCT CCACTGAAAC 420
CAGCTCCCTG GCCTCCGGGG GCCTCTCCCC TCCCTGGGCC TTCAGTCTCC ACTAAGGGGA 480
CAGGCTAGAG AGACCTCCCA AATCTTCTCC AGCTTGAATC TTCTGGGACA GCCCCTCAGA 540
TGAGAAGGTG AGATTTCAGC CCCCTGAGGA GGAAATTAGC AGAAACTGCT GAGTTTGAAC 600
TTGGATTACC AAGGTGCCAG CTGACTCCCG GAGTTTCTGG TGAGACTTTC GATTTCCTTT 660
AGCAGGCCTG CTGTGCTGAC AGCCGGCAGC AAACTCCCTC TAGGCCTCCT GGGTAGCTCT 720
CCCCAGCATC ATCTCCAACC TGGGTGCTTC CGAGGCTGCC TGGCCACGGC TCAAGGCTGC 780
TCAGGAACAG GTGGCCTCAG CTTGGAGACT ACCTAATGCC CTGCCCAGGA AGGCAACAGG 840
CTAACCAGCC TTTAACCTCT GTAAGTCCCA GGAAAACCAA CTGTTCATAG AACGAATCAA 900
CAACTTTGTG CTAGGTAAGA TCTAGGCTTC CACTCATTCT 940