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

TagContent
EnhancerAtlas ID
HS187-22259 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr7:1452000-1453040 
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
GTGCAGGTGC TGAGGTCGAT GTCACAGCTC TGGGGTCAGG GCCGCTGCCC TGGGATGGGT 60
CTGAGCTGTG CACGGCATTG CCTGGTGCCC TCCCAGCTCA AGGCCTTGCC TGACTACAGA 120
TGCTGTCCCT GCCTCGGGCC TGCCTGGCTG ACAGCGGGCA TCTGGGCCAG CGCTGCAATG 180
CTGCCAGGTA GAAGTGCTCC CTCCAGGCTG GGGGGACCTG CAACTCCCGC CCGGGAGTCC 240
CTCAGACTTG GAGTGCTCTG AAGAAAGCAA GCCAGCGGCC AAGTGGGCTA TGGGCCAGGT 300
GCGGGAAGGC TCCAGACCCG GGGCTGCAGG GTTGGAGAAG GGCGCAGCAA AGGCCTGGAG 360
ACAGCCTGAA CCAGGGATTC AGGATGGAAT GGGTCTGGGT CAGGGAGCCA GGGTGACCGT 420
GGGCCGCACA GGCCTGCGCG CGCGGGTGCA CGTGCGTAAT GGATGCACAC GCATGCAGCT 480
GGTGTGCGTG CAGTCGGGCG CACCTGTAAC CGGTGCGCAC CCCGCGTCTG GCGTGCAAGT 540
GGGAGCACCT GGCCCAGCGC CCAGCGGGGC CTCGCCCGCC GCTTTCTTAG GAAACGCCGC 600
AGCGCCACCT GCCGGCTACG CGGTCTCAGC TGGACGCGGG CGGGGAGGGC GCCGGGCCAC 660
GAGGCCCCGC CCACAGCCGG AGGCCCCGCC CCTAAAGACT ATCTTGGTGC CCCGCCTCTT 720
CAGACTCCGC CCGATTCCAG GCCACGCCCC TTGTAGGCGT GACCGAGGAC GCTGGTACCC 780
GGACCTGGAC TTCGCAGGGT CTTGGAGGGG CGGGCAGTGG GGGATCTCCG CTTTGGGTCT 840
CCTGGCTGCA AAGCGAGGAC AACTATGAGC CTTAAACGCA CACCAGGAGT GTAATAAGAG 900
CATCTGCTGC GTCACTAACT CTTCCCATTT ACCGATGAGG AAACCAAGAC AGAGAAGTCA 960
AGTCACCTGC CCAGAGTCAC GCAGGAGAAA GTCGTAGGCC GGCTTTGAGC CCAGCATCCT 1020
AGTTGCTGAG TCTCTGCAAT 1040