EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS040-16471 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr17:79069960-79072210 
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr17:79071185-79071196CCACACCCTGC+6.62
RREB1MA0073.1chr17:79072114-79072134CCCCCAAACTCCCCCTCTCC+6.2
ZEB1MA0103.3chr17:79071016-79071027GGGCAGGTGGG-6.14
ZNF263MA0528.1chr17:79070725-79070746GGAGGAGGAGGAGGTGGAGGA+10.16
ZNF263MA0528.1chr17:79070734-79070755GGAGGTGGAGGAGAAAGTAGA+6.34
ZNF263MA0528.1chr17:79070758-79070779GGAGAAGAAGGAGAAAGGAGA+6.43
ZNF263MA0528.1chr17:79070761-79070782GAAGAAGGAGAAAGGAGAGGA+6.66
ZNF263MA0528.1chr17:79070737-79070758GGTGGAGGAGAAAGTAGAGGA+6.72
ZNF263MA0528.1chr17:79070773-79070794AGGAGAGGAGGAGGAGGAGGA+6.85
ZNF263MA0528.1chr17:79070731-79070752GGAGGAGGTGGAGGAGAAAGT+6.8
ZNF263MA0528.1chr17:79070722-79070743TGTGGAGGAGGAGGAGGTGGA+6.91
ZNF263MA0528.1chr17:79070767-79070788GGAGAAAGGAGAGGAGGAGGA+7.48
ZNF263MA0528.1chr17:79070755-79070776GGAGGAGAAGAAGGAGAAAGG+7.53
ZNF263MA0528.1chr17:79070740-79070761GGAGGAGAAAGTAGAGGAGGA+7.79
ZNF263MA0528.1chr17:79070752-79070773AGAGGAGGAGAAGAAGGAGAA+8.01
ZNF263MA0528.1chr17:79070764-79070785GAAGGAGAAAGGAGAGGAGGA+8.3
ZNF263MA0528.1chr17:79070776-79070797AGAGGAGGAGGAGGAGGAGGC+8.51
ZNF263MA0528.1chr17:79070728-79070749GGAGGAGGAGGTGGAGGAGAA+9.37
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_25200chr17:79070885-79072115Colon_Crypt_3
SE_26560chr17:79058335-79072649Esophagus
SE_31420chr17:79065869-79071978Gastric
SE_34261chr17:79065007-79076982HCT-116
SE_42160chr17:79070033-79072181Lung
SE_57453chr17:79068914-79072091VACO_503
SE_65191chr17:79070565-79072072NHEK
SE_65309chr17:79065152-79072658Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177907038979072210
Number: 1             
IDChromosomeStartEnd
GH17I081089chr177906372979072490
Enhancer Sequence
TGGCTCTGGG CAGCCCCCTG GGCCTGCCTT TTCTCAGTGC CTCAGTTTCT TTTGCCAGGC 60
GTTGGATCTC CTGCTGAGTG CTCTCTGGCC CTGAGCTCTC TGCCCACCAT GCTTTCCGGG 120
CCGGCCACCG CTGGAAAAGT CCCCAGGGAG GGCACAGAAT CCTCATGATG GGGTGCGTTG 180
GGGGTTTCTC CATGGAACCT CACACACATT CCTGAGGCTG CCCCACTTAA GGGATTCTGG 240
GCACCGAATA GCTCCCTCCA AAGCAGGCAC CCCCATCACA GGCCACTCAG AGCCTGGAGG 300
CGCACCCCAG CATCCCTGGC AGTTCCCTGC GGGAGGAGCG GGGCAGGACC CTGCAGGCGG 360
CCTTGGAACA GGCCTGGGTG TTGGTCTGAG TGGTGTTGCA GGGGCATGGG TGGGTGCTCA 420
TCTCCAGGCC CCTCCTTGTG CACAAGCCCA CTTGTTTCTC GGAGCACACC CTCCCCACCC 480
AGTCCCTTTG ATCCTGAAGG TCAGGAAAGG AGTCCAGCAG CCAGGCTGAG GCTGGAGCAC 540
AGCGGGCTCA GGTGTCCTCC TCCATGGCTG CAGTATGTGG CGTCCTGGCC ACGGCCATCA 600
TGCCCTCCCC AGGCCCCAGG GTACCCCTGA ATCTGGCTGT CGCACTCTAC CCCTTCCTGG 660
AGAAGGAGCC TCAGAGGTCA CTGGAGGTTC TTGGGAGCAG GAGCAGGAAG CCCTGGTAGG 720
TGCATGTTGC ATAACCAGAG GAAAAGTACT TCGCGCTCCA GCTGTGGAGG AGGAGGAGGT 780
GGAGGAGAAA GTAGAGGAGG AGAAGAAGGA GAAAGGAGAG GAGGAGGAGG AGGAGGCAGC 840
GGCAGTGGGG GTGGCGGCAG AGGCCTCAGC ATGGAGCAGA GCTTGCTGGA AAGTCTGCTT 900
AAGGTTGCCT TGCAGGGCCT CTCACCTGTG ATCAAACTTC TCACTTCCTA AATGCCATCT 960
CAGGTCCCCT TTAGGTGACC CTGTGGCCAG GCCCTACAGC GCCTCTGGAG GGTCAAGGCC 1020
TACTGGGGAT AGGAGTAGCA AGCCCGTTGT TTTGAGGGGC AGGTGGGGTT TAGTGTGGGA 1080
AAGCAGGGTG GGCTGCAAGG GCAGGGGAGC GCCGGGCTCC GTGTTGGGGG ATGTGGCTGG 1140
GCAGGCTCTG GCCTTGGGGA CAGCATGGTC TGCTCACACT GGCCAGCAGG CAGAGCCAGT 1200
GCCCGGTGGT AGTGCTGGGA CCGACCCACA CCCTGCCAGG CTGGTTCTCA CCCCTGTAGT 1260
GGAGGCTTGC GGGGGTAGGC AGCCAGGGAA CAGGCTGCTC CGCTCCCCTC CCCGCCGCCC 1320
ACCCGGCCCG GCACTGCCCA CCCACGCTGA GTCAGAGCTG TAGGCGGGGC GGCCGCGAGG 1380
CTGAGTCAGG CAGGGGAGGC CGCCCCCTTG CGGAGGCCGC ATCTTCTTAA GAGCCGATTC 1440
TGAACTGACC ACTCCTTGAC GGGCAATCCC GGTGGACGGG GGGTCTGAGT CCTGCTGTGG 1500
AGGGTCTGCC TGAGGCCGGT AGGGGCTCAG CCCAAGGTAG GTAGGCACAG GAGGAGAGGC 1560
GAGACAGAGG AGAGCTGGAA AGACCTTCCT GGCAGAGGAG AAGCTGGCTC CCTGCTGAAG 1620
CAGCTAGCCT CCTGCGGCCT CCCAGGAGGG GCCTGGGTGT GTCCCTGGGG ACAGGGTCTG 1680
TGCCTCGGGT GCTCCTCCCT TGCCCTCACC AGCCACCCAC AGCCTCATCA GCGTTTTGGG 1740
ATGGAAAGTT TCCAGCCTAC AAAACCGGAG AGCCCTTGAC ATCCAGGGTC CCAGTCGAGC 1800
CCTCCCACTG TCGGGCTGGG GTTCTGGAAT CGGGAACCCC GGGTGCCGGG TGTCAGCTGT 1860
GCCATAGGGC TGTGGTGTCA CGCGCTACCC CAGACCTCAG GCACATGATC CCCAGGCCAG 1920
CTGGGGTCAT GGAGGGGCCA GCGGGGGGTG GGGAGGCATG CTCCTCCCAG AGGGACAGAG 1980
GCAGAGAGCC CTGGGGTTTG GAACTGTCAC TTCCACCTAC AGCCCTGTTG GTCAGGTGAG 2040
TCATACAACA AGCCCTGCAC CCATGGGCAG GCTGGGAGGC GCCTCTGCCC AGGATGGGAG 2100
CACAGTCCGG GGCCTGGGAG GCAGCGGCCG CCCTCAGCTT CTTCGCCACT CTCTCCCCCA 2160
AACTCCCCCT CTCCAGTTTC CTCCCGAGGC TCACGTTGGA GAGGCCTGGG CTCAGCTACA 2220
GTTTCTTGGT CTGGCTTTGC TTGCACTACT 2250