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

TagContent
EnhancerAtlas ID
HS042-29920 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr22:25208630-25210040 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6004297chr2225209780hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr22:25209055-25209073GGAAGGAAGGGAGCAGTG+6.42
EWSR1-FLI1MA0149.1chr22:25208761-25208779ACTTCCGTTCTTCCTTCC-6.7
EWSR1-FLI1MA0149.1chr22:25209051-25209069TGAAGGAAGGAAGGGAGC+6.82
EWSR1-FLI1MA0149.1chr22:25208765-25208783CCGTTCTTCCTTCCTTCC-7.8
EWSR1-FLI1MA0149.1chr22:25208769-25208787TCTTCCTTCCTTCCTCCC-8.52
NEUROD2MA0668.1chr22:25209769-25209779ACCATATGGC-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr222520923225209422
Enhancer Sequence
GAGCAAGGGA GGGTTTTGCT TAGGGCTGTA CTTCAGGAAG TTTCAGCTAA TAGCAGGGAC 60
CAGGATAGAC AGTTTCTGCC AACTCTTAGA AGAAAACTTT CTCCCTCCCT CTGTTATTTT 120
CTTTCTCCCC CACTTCCGTT CTTCCTTCCT TCCTCCCACA AATATTTATC AAGCATCTAC 180
TATGTGCCAG GCCCTGTTCT ACAAGCTGCA AACTGAGAAG TGAGTAAAGC AATGTCTTTG 240
CTCATATGCC CTCATTCAGT GTACAGTATA GTGGCAGGAG GGCATATAGA GAAAACAAGA 300
AATATGTATT AAAGGTAACA AGAGCTCCAA GGAAAATAAC GGCTGGAAGA GATGGGAAAG 360
GCTTGCCAGA GGAGGTGGTC AGGGATGGCC TCACTGATGG GATGGTGTTT GAGCAGAGAC 420
CTGAAGGAAG GAAGGGAGCA GTGTCAACAT CTACAGGAAG TGTGTGCCTG GCAGAGGGAA 480
TAGCGTATGC AGAGGCTGTG AGTTGGGAAC AGACCAGCTG GGAGGCCAGT GAGGCTGGAG 540
TGAAGTAAAC AAGAGTAGAG ATGAGGTTTG AGAGAGTGGG AGGCTGATTG TTCAAGACCT 600
TGTCCATCGA AGGCATCGAA GGCTTTGGCT TTGACTCTGG TGAGATAGGA GCCATGGGAG 660
TATTCTGAGC AGGGGAGGAA CAGGCAAGTT TTGGGGACAA GTTGAGAGGA AGCAAAGACA 720
CCAGATCATC AGATAAGACA GGAAACGTCT GCCTTTGCTA AGCTTTTCCA TTCTTGGGCT 780
GGAATCACAG CCCCCCACCC ACTACTCGCC CCACTGTGCC AAGGAGAGAC TCCAAAAATG 840
CATGTGCTTG AATGAATGCA GGAATGCCAG GTGGGCTATT TTGGGGCTCT CCGATGCTGG 900
CAGGATTGAC TCAAATCAGC TTGCGTGTGT CGTGTTTGCT GGCTTAAGAG GGCAGAAACG 960
CTCCTCATGA ATAATGCAGC CATATCCACC CGATGCGTTT TGATGCTTTT TCAGGTCTCT 1020
GGCAACCTGG CTTCTGGGAG CTTTTGCTAG TGATGAGCAT CTGTGGCAGC TTAGGCACCC 1080
TGGTTCGATG TGGTGAGGAT GGCAGGAGGG CCCCTGGCTT GCCTGGCTGT GTCTCTTGTA 1140
CCATATGGCT GGGTCTCCCC CAGCCACCTC ATGAGGTGCT CCAGGAGCTG GTGGTAGCAT 1200
TTGTTGCTGG CTGGCCGGTA GGAAAGGGCA TTTTGGTCAC CCCTAAGGGC CCGCAGTTGC 1260
TGTCTGCAGA GCCCAGGATG GGAGGTGAGG AGACCTGTGT CCTTGTTCCA GTTCTGACCC 1320
CAACAATGCT TGTGGCTCCT AACAGGTCCC TTCTCAAGGT CTCACTTTCC TGCTTTCTAA 1380
GTGGACGAGG TTGGACAGCT CCAGGATTCC 1410