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

TagContent
EnhancerAtlas ID
HS120-04311 
Organism
Homo sapiens 
Tissue/cell
LNCaP-abl 
Coordinate
chr22:24255630-24256800 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr22:24255933-24255951ATTTCCTTCCCTCCCTCC-6.45
KLF16MA0741.1chr22:24256256-24256267GGGGGCGGGGC-6.02
KLF16MA0741.1chr22:24256352-24256363GGGGGCGGGGC-6.02
KLF5MA0599.1chr22:24256257-24256267GGGGCGGGGC-6.02
KLF5MA0599.1chr22:24256353-24256363GGGGCGGGGC-6.02
SP1MA0079.4chr22:24256351-24256366CGGGGGCGGGGCTTG-6.23
ZNF263MA0528.1chr22:24255838-24255859CTCTTCCCTTCTTCTTCCTTC-6.61
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_37758chr22:24249966-24257197HSMMtube
SE_56738chr22:24255405-24256233VACO_400
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr222425599724256450
Number: 1             
IDChromosomeStartEnd
GH22I023907chr222425015724258315
Enhancer Sequence
GAGGTCCCTT CCTGTCACAA CAGCTGGGCT CCTGACTCAG ACCAAGACAG CTTTTGTTTC 60
TTTTCCTTTC TAGCCCCCCA CTTCCCACCC ACCTTTCTGC TTTCTCATAT GGGCTCATTA 120
TGGTTTATAG GGCTGGGGAA CGTTGCCTCT TCTGCCCTCC ATTTCTCCCA TCTCCCTTCT 180
TTCCCCTCCA CTTTTTCTGA GTCCACTTCT CTTCCCTTCT TCTTCCTTCC CTCTGGGACG 240
CTGCACAGTT CCTTCCACCC GGCACGGCCT GGGACTCTAG ACTCCCTCTG AAGGCACGGA 300
AGTATTTCCT TCCCTCCCTC CGACCCGATC TTTCTGCCCT TGATTCAAAA CAATCTGAGG 360
TCCCTAGGCC CTTCCCTTTC CGCCTCTGCG CTCCCCATGG GGTCCGGTGT AGTTTTCCCG 420
CCCCTTCCCT GCAGCTCCCG AGACCACCCG GACACAACGG AGCCATCCAG CGCCCTCAGA 480
GGCCCTGGGC ACACGGGCAG ATGGTCACCG CCTCCTAAGG GAGCAGCGCG CGCCCGTTGC 540
TCGCTGCCCG TTGGTTGTTG CTGGTAGCTC CGGAGGGCGG GGTTGGCGAG GAAAGTGAGT 600
CCGTATGTCC CCAGCATGCT CCGCGCGGGG GCGGGGCTCT AAGGGGGCAG GCGAAGGCGG 660
AACTGGCGTG GTCAAACCAA CCTATCAGCC TCCAGCATGC TCCGTGTGGG AGCGGGGTTC 720
CCGGGGGCGG GGCTTGGTTT GTGTGCCCTT CCGGCGTTTC GCCCCTGCGT TCTCTGAGAT 780
GCTCCCACGC AGATGTATGG GCCTAATTCG CTAATATCCA CTCTATATCC TGTTCCATCC 840
TCTTGTAATG GGCGTTTGGA GTGTTGCCAA TTTTTTGCTG TTATAATGAT TGTAATAGCA 900
TATTAAAAAA CTTGAACATA GTTTGATTGT AATAACATTA AATATAGCAT CTTAAACATA 960
CAGTTTGAGC GTGCCAACCT GATGGGTGTG GAATGTAATA TTCATTATAA CTTTGATTTT 1020
CATTTCCCTA CTTTGAGTAA GTTTGAACTT CTCTTTATGT AATTATTGAC TACTCTGTTT 1080
TCATGTTCTG AGAATTGCCT GTTTGTATTT TATGCCCATT TTTCTATTGG GTTGTGGTTT 1140
TTATTGATTG GTAGTTCTTT ATAATTTTAT 1170