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

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EnhancerAtlas ID
HS007-15124 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr7:2183200-2184600 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
STAT3MA0144.2chr7:2183441-2183452CTTCTGGGAAA+6.62
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr721836852183911
Enhancer Sequence
ACCCAATGAC TCTCGAGTCC CTTATGCTTG ACAAGGGCCT GACTCCTCCT GACGCTGCCC 60
AGGCCCCTGA TGGCAGCAGT AGATGAAACA GGCCAGGCCC AGGCACCTGG AAGCACCACA 120
CGGCCAGGTG CTCCAGGACA TGCCAGCCTT GTGGCTTCAG GCCAAGGGCT CTTCTGCCTG 180
GAGGCAGCAA GGTGGGATCT TCAAAACAAA CTGCGGCGAT CACAGCCCAG GCTGGAATGC 240
ACTTCTGGGA AAGCCGATGC ACAGAGGGGA GGCAGGGGAG GCCAGGGCAG ACCCCAACAT 300
GAAGAGCTCC ATCTGCATCC ACGGCCCTCA GGGGCTCCCC TCTGTGGACT TCTCAGCCGG 360
CTCTACCTTA AGTCAGCATC GAGGAGGATG CCTGGGGCTT CAAACAGGCA AAACAGCACC 420
AGGCAGGATC CATGACCCAG GGTCTCTGCT GAGGCAGAGA AGCAAGGCCA AAGCCGAGAC 480
GGCAGCCACA CAACGTGTCC CACAGGGACC CAGGAGCCAC CTGCAAACAC ATCCCACAGA 540
GCTCTGGAGA CCCACAGGCC TGGACGCACG TCCTGCTTTC ACCACCTCCC AGCTGTTTAG 600
CCCGGGGCTC AAGTTCCTCC CTGCAAAAGA GGGAATCATA AGAGCTTCCA GCTGGGAGCG 660
TCTGTGAGGC TCAAGTGAGA GGCTGCGCAT GAAGCACAGC GCAGCGCATG GTGAGGGCAG 720
ATGCGAGACA AACACTGACT GCTCTCAGCG TCCCCATCGT CATTCATCGC CGGGATTACA 780
GATGATACAC CTGAACCCTG GAGCCCTCAC GGGGTCCTGA GAGGCCCCGC TCCCGCCACC 840
AGCCCTCTCC AAAGCACGGT CTTATTTCCA GCACAGCAGA GAAACCGCCA AGAGCATGGC 900
CCCACGCATC CCTGCCCGAG CTTCCCAGCC CTGTTCTTCA CGAGCCCTCA GAGCACGCTG 960
GCCTATTCCC CCCCAGATCT GAAAGATGAC AGCATGGCCA CGGGCTGGGC CACAGAGGAC 1020
TGCAGCCTCC TGTCCCGGCT CTTCCCACGG CAGAGCTGGG GACGCCAGGC AGAGGGGTGC 1080
TTGGGTCCCT AAGGGCCAAG GAGACTAAGA GGGCCCGGAA AGGGAAGGGA GGCTACAGGG 1140
CAGCCCCGGG GTGCCCTGTG TGAAGCGTGA GCAGAGGGCG CACCAGATCC ACCCACTGAT 1200
TCTGAACAGT ATGCCCTGTC CTCAGCCCCA CAACCAGGAG GTCCATTCTC AGATTCTAAG 1260
AGCCGAAACG AGGCTTGAGC GTAAACCAGG CCAGGCTCCC CTACACTGCC ATGAAGCTCC 1320
TGCTCCAAGG TAAAGAGGCC CAGGATCTCT GACACGCTCT GCTCACACCA GTGACCAATG 1380
ACGCCCCATC TGTCCACGGC 1400