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

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EnhancerAtlas ID
HS080-00565 
Organism
Homo sapiens 
Tissue/cell
H9 
Coordinate
chr1:25844020-25844890 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr1:25844756-25844768AAACAAACATAC-6.37
INSM1MA0155.1chr1:25844113-25844125CGCCCCCTGCCA-6.07
KLF16MA0741.1chr1:25844109-25844120GACACGCCCCC+6.32
MYCNMA0104.4chr1:25844771-25844783GACCACGTGGCG+6.07
MYCNMA0104.4chr1:25844771-25844783GACCACGTGGCG-6.07
NFYAMA0060.3chr1:25844276-25844287GGCCAATCAGA+6.02
SP8MA0747.1chr1:25844109-25844121GACACGCCCCCT+6.27
TFAP2AMA0003.3chr1:25844581-25844592TGCCTGAGGCT-6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12584422525844803
chr12584454425844811
Number: 1             
IDChromosomeStartEnd
GH01I025518chr12584458125844710
Enhancer Sequence
ACTCTTACCG CAATGGTAAG CAGGTGCTGG ACACGAAAAA CAGGAGATGC TGCTGACACC 60
TGGGGGAGGC CTGTCCCCAC CCACTCAGAG ACACGCCCCC TGCCACCGAT CCAGGGAAGT 120
GCGCAGCAGG TCAGCCTTTG GCTGCCGTCA GTCGGCCAGT CTCCCACATC TCTGGGACTC 180
CTCTTGCCAC GTCGCAGCTG GGAGAGGCCT AGGGAGAGGG GCTGTGTGCA CGGATTGGCA 240
GTGGGAGAGA GATGTAGGCC AATCAGAATA TCACGCGGGT TGGAAAGGGG GCTACTGTGC 300
GCGAGGTGCC TTCTCGTGCC CTGCCTCAGT GGGACCCTCA CCTTAGCTCC GTGCAGGTGA 360
GGAGGCTGGG CCTGGGCCAA GCTCTCACAG CTACAGGGTG CTGGGTGGAA GGGGGCCTCC 420
TGCACTCGGA GCTCTTGGCT TGTCTCCACC CAGCAGCTCC CTTGAGGAAG GTGGGGAAGG 480
TCGCAGCTTT GTGCAAAGGG AGCGAGTACA CAATGTGGCC GCCTCCTCTT TTCCATCCCA 540
TCACCTCTCA TTTCACCAAC CTGCCTGAGG CTGCAATCAA CACTCCCCGC GTGTGGGGGC 600
GGAGCCAACC CACGAGGCCA TGCTTCAGGC CCCTGATTGG TTCAGGAGTA GCGCTTGACC 660
TAATGAGGCG CTACCAATGG GATGCAAAGA GACGTTCCCT GGCCTTCTGC CAGAGCGGTT 720
TCCCTGTTCT CCCAACAAAC AAACATACCT GGACCACGTG GCGCGAGGAT ATTAAGTTTA 780
AGATGGTGGC AGCAGTTTTT GAGACCTTGC AGAGAGAGCT GCTGAAAGCT GCTGGGGGCG 840
CAGCCTCTCA GGTTGTACAC GAGGTGCTGA 870