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

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EnhancerAtlas ID
HS184-18272 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr20:44621910-44622700 
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr20:44622305-44622316GGGTGACTCAG+6.02
JUNBMA0490.1chr20:44622305-44622316GGGTGACTCAG+6.02
NR2C2MA0504.1chr20:44622544-44622559TGACCTCTGACCCCT-9.03
Nr2f6MA0677.1chr20:44622544-44622558TGACCTCTGACCCC-7.03
RxraMA0512.2chr20:44622544-44622558TGACCTCTGACCCC-6.98
ZNF263MA0528.1chr20:44621959-44621980AGAGGAGAGGCGAGGGGAGGG+6.23
ZNF263MA0528.1chr20:44621934-44621955AGAGGAGAGGAGAGGAGAGGG+6.29
ZNF263MA0528.1chr20:44621981-44622002AGGGGAGGGGAGAGGAGAGGA+6.69
ZNF263MA0528.1chr20:44621939-44621960AGAGGAGAGGAGAGGGGAGGA+6.86
ZNF263MA0528.1chr20:44621971-44621992AGGGGAGGGGAGGGGAGGGGA+6.91
ZNF263MA0528.1chr20:44621944-44621965AGAGGAGAGGGGAGGAGAGGA+6.95
ZNF263MA0528.1chr20:44621976-44621997AGGGGAGGGGAGGGGAGAGGA+7.1
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr204462213244622355
Number: 1             
IDChromosomeStartEnd
GH20I045992chr204462141044623020
Enhancer Sequence
GAAGGAAGGA AGGAAAAAGA AAGGAGAGGA GAGGAGAGGA GAGGGGAGGA GAGGAGAGGC 60
GAGGGGAGGG GAGGGGAGGG GAGAGGAGAG GAGGAAATTA GAGGACCCCT GAGTCAGGGG 120
AAGCTACTCT AGTCTCTAAG GTCAGCCTGA GTGGGGTTTT GGGGTGCTTT GCAGGGAAGA 180
GAGGAACCTC GCCTGCTCTC TTCGCAGGCT CCAGGTCTGC TCTGAGCCCA CATCTGCCCG 240
AAGGCATGCC CGCTGGGGTG TTCCTTGCTG AGCGAGTGAG GCAATCCCTG CAAGGGAGGT 300
GTGGTGGTTC TGGCGTGAGC CTGAACCTTG GGGCAAGAGG GAAGGACAAT GTACTTCTCA 360
GCCATTGCAG GGTGTGTGTA ACCTGCCCTG CCAGTGGGTG ACTCAGGCTG AAACCAGACC 420
CAGCATTCAC CCTGTCTAAG CCTAGTTGGT TAGTGTCTGG AGTGCTGTCA ATTGCTTTAC 480
ATTTGCCCTT CAGGGAAATG CTTTTGCACT GACAGGCGGG GCCCAGATTG GAGGTTGTCA 540
AATCTGCAAA GCCCTACTCC TCCATTTCCA CATGGCAGAC TCCTATTCAC ACTCCAAAAC 600
CCGGCCCAGG TAGTGCTCCT GCTGAACCCT TTCCTGACCT CTGACCCCTC CCCCATGGAG 660
TGAATAATGT TGTCTTCCAA TATGCACTCT GGAGCCAGAC TGCCTGGGTG TGAATCCCTT 720
CTCTGCCACT TACTAGCTGT GTAATCTTGG TCAAGTTACT TAACTTCTCT GTACTTCTAC 780
ATCTGCGGAA 790