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

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EnhancerAtlas ID
HS023-12791 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr19:19652060-19653180 
Target genes
Number: 9             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs8102502chr1919652746hg19
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EGR1MA0162.3chr19:19652253-19652267GGTGCGGGGGCGGA-6.01
EGR3MA0732.1chr19:19652253-19652268GGTGCGGGGGCGGAG-6.5
KLF16MA0741.1chr19:19652211-19652222GGGGGCGGGGC-6.02
KLF5MA0599.1chr19:19652212-19652222GGGGCGGGGC-6.02
NFAT5MA0606.1chr19:19652780-19652790ATTTTCCATT+6.02
NFATC1MA0624.1chr19:19652780-19652790ATTTTCCATT+6.02
NFATC3MA0625.1chr19:19652780-19652790ATTTTCCATT+6.02
SP1MA0079.4chr19:19652210-19652225TGGGGGCGGGGCCTC-6.44
SP4MA0685.1chr19:19652208-19652225GTTGGGGGCGGGGCCTC-6.37
ZNF263MA0528.1chr19:19652096-19652117GGAGGAAGGGGAGGTTAGGGG+6.25
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191965272019652967
Number: 1             
IDChromosomeStartEnd
GH19I019539chr191965039319652871
Enhancer Sequence
AGGGGCGGGG TCTGGAGGCT GGGACCTGTA CAGAGGGGAG GAAGGGGAGG TTAGGGGCTG 60
AGCCTGGGAG AGAGGGTGGA GTTAGAGGCG GTGCCTGGAT GTAGAGAGGC AGTGCTTCTC 120
CTGAGCGATG CCTAGAGGGG AGGAGCTAGT TGGGGGCGGG GCCTCGTGGA CGGGGCTGTG 180
AAGGGCGGGG CCTGGTGCGG GGGCGGAGCC TGGAGGACCC AAACTCTGGA GCCAGGTGGA 240
GACCAGCCCT TCCTTCCCTC CTGGGCCCAA GGAGCACTGG TAACTATGCA CATCTGGACA 300
GGTGGATGCC AGGGGGCTCT TGTGCAGGCA GACATGGGCA GATAGGAGGG GGTGCTTCCC 360
CTGTGTGCAT TCCAGACTGT ACAGATGTCT TCGTGGGGAA ACAGAATTCA GTTCATGCAC 420
TCAGGGTGCA CACGTGCATG GCATTTGCAG CCCCCACCCC GGTCCCCCAC GCCCACACAG 480
ACACCCGCTC ACAGCCTGGC AGACATGATG CCTAGGCCCT CCCAGGGCCA GACACCGGGC 540
AAGCCAGGAG GAGACTGGAA ATTCCGCTAG CGCCTGGGCT CCACAAACAC GGCCTGGAGG 600
CTGCTCCGGG GAGCCCGTCA CAGGGTGGGG GCACATGGTG GCCAATGGGG CGTTGGGGTC 660
CCCACCCCAT CGCGCCTGGC TCTGCTCTCC CGGTGCCTGT GCCCTGAAGT TTCCAGTGGA 720
ATTTTCCATT TTATGGAGAA ACCGCAGGAT TGGGAAGGGG GGCAGTTGTT CTCAGCCCAA 780
GATCCAGCCC CTTACTGGGC CCCCAGCCCC TGTCCAGACA TTTTCTCTTC TGCTGGAAAG 840
GGCAGTGCCA TATTTTGAGA CTTACCTCTC CTGTCCCCTC CTATAGGACC TCTTCCCTAC 900
GTCTCTGGAT CCCAGTTCCT ATGCCCTGGC CCAGTCCTGA CCACTTAGCC CATCTCCCCT 960
TCACACTAGG GACTGCTCCA AGCAGGGCCA TGCTGAGGCC TCTGAGAGGC ACCTTATGGG 1020
GGGGCCCCAG GCATATTTGT TGAGTGACTG ATTGAATGGA AAGCCCTCCT CAGGAGGGAG 1080
TGTGAAGGTT TCTCTGTCCT GCTTCCTCTC CATATCCCCC 1120