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

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EnhancerAtlas ID
HS048-33232 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr7:1452080-1453020 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr7:1452599-1452618CAGCGCCACCTGCCGGCTA-6.78
KLF13MA0657.1chr7:1452738-1452756AGGCCACGCCCCTTGTAG+7.34
KLF14MA0740.1chr7:1452739-1452753GGCCACGCCCCTTG+6.08
KLF5MA0599.1chr7:1452682-1452692GCCCCGCCCC+6.02
SP1MA0079.4chr7:1452679-1452694GAGGCCCCGCCCCTA+6.06
SP1MA0079.4chr7:1452660-1452675GAGGCCCCGCCCACA+6.45
SP1MA0079.4chr7:1452737-1452752CAGGCCACGCCCCTT+6.7
SP3MA0746.2chr7:1452739-1452752GGCCACGCCCCTT+6.02
SP4MA0685.1chr7:1452660-1452677GAGGCCCCGCCCACAGC+6.13
SP4MA0685.1chr7:1452737-1452754CAGGCCACGCCCCTTGT+6.76
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr714522001452525
Number: 1             
IDChromosomeStartEnd
GH07I001411chr714514881453169
Enhancer Sequence
CCTGGTGCCC TCCCAGCTCA AGGCCTTGCC TGACTACAGA TGCTGTCCCT GCCTCGGGCC 60
TGCCTGGCTG ACAGCGGGCA TCTGGGCCAG CGCTGCAATG CTGCCAGGTA GAAGTGCTCC 120
CTCCAGGCTG GGGGGACCTG CAACTCCCGC CCGGGAGTCC CTCAGACTTG GAGTGCTCTG 180
AAGAAAGCAA GCCAGCGGCC AAGTGGGCTA TGGGCCAGGT GCGGGAAGGC TCCAGACCCG 240
GGGCTGCAGG GTTGGAGAAG GGCGCAGCAA AGGCCTGGAG ACAGCCTGAA CCAGGGATTC 300
AGGATGGAAT GGGTCTGGGT CAGGGAGCCA GGGTGACCGT GGGCCGCACA GGCCTGCGCG 360
CGCGGGTGCA CGTGCGTAAT GGATGCACAC GCATGCAGCT GGTGTGCGTG CAGTCGGGCG 420
CACCTGTAAC CGGTGCGCAC CCCGCGTCTG GCGTGCAAGT GGGAGCACCT GGCCCAGCGC 480
CCAGCGGGGC CTCGCCCGCC GCTTTCTTAG GAAACGCCGC AGCGCCACCT GCCGGCTACG 540
CGGTCTCAGC TGGACGCGGG CGGGGAGGGC GCCGGGCCAC GAGGCCCCGC CCACAGCCGG 600
AGGCCCCGCC CCTAAAGACT ATCTTGGTGC CCCGCCTCTT CAGACTCCGC CCGATTCCAG 660
GCCACGCCCC TTGTAGGCGT GACCGAGGAC GCTGGTACCC GGACCTGGAC TTCGCAGGGT 720
CTTGGAGGGG CGGGCAGTGG GGGATCTCCG CTTTGGGTCT CCTGGCTGCA AAGCGAGGAC 780
AACTATGAGC CTTAAACGCA CACCAGGAGT GTAATAAGAG CATCTGCTGC GTCACTAACT 840
CTTCCCATTT ACCGATGAGG AAACCAAGAC AGAGAAGTCA AGTCACCTGC CCAGAGTCAC 900
GCAGGAGAAA GTCGTAGGCC GGCTTTGAGC CCAGCATCCT 940