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

TagContent
EnhancerAtlas ID
HS002-09047 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr7:100802910-100803790 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2074683chr7100803614hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr7:100803086-100803097GATGAGTCACC-6.32
JUNDMA0491.1chr7:100803086-100803097GATGAGTCACC-6.62
PLAG1MA0163.1chr7:100803442-100803456CCCCCCAGGGCCCC-7.03
ZNF263MA0528.1chr7:100803137-100803158TGAGGAGGGGGAGAGATGGGG+6.01
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_34567chr7:100802020-100808455HCT-116
SE_65756chr7:100801977-100804101Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr7100803006100803372
Number: 1             
IDChromosomeStartEnd
GH07I101159chr7100802601100808148
Enhancer Sequence
TTTAACACAC ACATACTCCA AAGCCTCTGC GTCTCAGGAG GAAAAGGCTA TGGGGATTTG 60
GGGGCTGGCA GAGGGCACCT GGATGTTGGT TCTCCCTGCT CCCCAGCGCC CCCGCCCTCA 120
CCCCATTACT GCCTGCCCCC TCTCTGCTGT GCCATCACCG AGCCCTGGTG CAGGGAGATG 180
AGTCACCGGA ATCTGCAGTG ATGAGCGAGC CCGGCCTGAG CTGGCTCTGA GGAGGGGGAG 240
AGATGGGGGG CGAGGGAGGG CTCATCTTTG CAGTGGGAGA GAGGGCAGAA CTGAACTTGC 300
CACCTCACTG GTCGAGCTTC ACCTTCCCAC ACACGCACAC ACACACACCC TGGCGCGCAC 360
ACACACACAC ACACACACAT GCCCTGGCAC ACACACCCAT CGTGTCACCA GTGTTGCGCT 420
CAGACCCTAA TGACGCATCT CCCTGCAGCC TGGTTCACCT TCCCTCAGGG ACCTGGCACT 480
CACCTCCCTC TGCCTTTTCC CCACTCTGAA AAACAGGACC CAGTCAGCTG TACCCCCCAG 540
GGCCCCAGAA AGATCCCCCA CCTCCTTGTC CCGGCTTCAC TCCCTTTACC CCCAGGTGTC 600
AAGGCGGGGC CCCTGCTTAC CAAGGTCCTG GCTTTGGGTT CTCTGGGTGG TGACGGACTC 660
AACCTGGACC CCCCCTGCCA CTGTTGGCTG GCTCTGGGGC TGGCCCTGGG AGGCTGGTGG 720
GTGCCCCATG AAGGGCTCAC TGGTCCGGCC TTGGGCTCAC ATTGGCTTCT CTCCCCCTCC 780
CCCGTGTCTG TGCCTCCCCC GTCTGACTCT TCCTCGTGAC TGCTGTCTTG CCCACCCTGT 840
CGGCCTCTCC TGGTGTCTCT GCGTCACCCT CTGTCTGTCT 880