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

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EnhancerAtlas ID
HS047-30245 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr7:1452010-1453260 
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
TGAGGTCGAT GTCACAGCTC TGGGGTCAGG GCCGCTGCCC TGGGATGGGT CTGAGCTGTG 60
CACGGCATTG CCTGGTGCCC TCCCAGCTCA AGGCCTTGCC TGACTACAGA TGCTGTCCCT 120
GCCTCGGGCC TGCCTGGCTG ACAGCGGGCA TCTGGGCCAG CGCTGCAATG CTGCCAGGTA 180
GAAGTGCTCC CTCCAGGCTG GGGGGACCTG CAACTCCCGC CCGGGAGTCC CTCAGACTTG 240
GAGTGCTCTG AAGAAAGCAA GCCAGCGGCC AAGTGGGCTA TGGGCCAGGT GCGGGAAGGC 300
TCCAGACCCG GGGCTGCAGG GTTGGAGAAG GGCGCAGCAA AGGCCTGGAG ACAGCCTGAA 360
CCAGGGATTC AGGATGGAAT GGGTCTGGGT CAGGGAGCCA GGGTGACCGT GGGCCGCACA 420
GGCCTGCGCG CGCGGGTGCA CGTGCGTAAT GGATGCACAC GCATGCAGCT GGTGTGCGTG 480
CAGTCGGGCG CACCTGTAAC CGGTGCGCAC CCCGCGTCTG GCGTGCAAGT GGGAGCACCT 540
GGCCCAGCGC CCAGCGGGGC CTCGCCCGCC GCTTTCTTAG GAAACGCCGC AGCGCCACCT 600
GCCGGCTACG CGGTCTCAGC TGGACGCGGG CGGGGAGGGC GCCGGGCCAC GAGGCCCCGC 660
CCACAGCCGG AGGCCCCGCC CCTAAAGACT ATCTTGGTGC CCCGCCTCTT CAGACTCCGC 720
CCGATTCCAG GCCACGCCCC TTGTAGGCGT GACCGAGGAC GCTGGTACCC GGACCTGGAC 780
TTCGCAGGGT CTTGGAGGGG CGGGCAGTGG GGGATCTCCG CTTTGGGTCT CCTGGCTGCA 840
AAGCGAGGAC AACTATGAGC CTTAAACGCA CACCAGGAGT GTAATAAGAG CATCTGCTGC 900
GTCACTAACT CTTCCCATTT ACCGATGAGG AAACCAAGAC AGAGAAGTCA AGTCACCTGC 960
CCAGAGTCAC GCAGGAGAAA GTCGTAGGCC GGCTTTGAGC CCAGCATCCT AGTTGCTGAG 1020
TCTCTGCAAT CAACGACTGC CCCCAACTCC TAGTAAATTC ATCTTTATTT GTTAATTAAT 1080
AGTTATTTAC GAGAATAAAC CCATCCAACC TCCCACCCCT TGCAATAGGT ATCTGGGAAG 1140
TGATGGAGAC AGGCATTCTG AGCTGTCACC AGTATCTTAC ATGGCCAGAA AGGTGGAGTT 1200
CAGGGAGAGG ATTCTCAGGA TTTGGGGGCA AAATGAGTTA GGAGACCGGA 1250