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

TagContent
EnhancerAtlas ID
HS187-21072 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr6:33823670-33825730 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2104362chr633825358hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr6:33823800-33823818GGAAGGAAGGAAGCAGTA+6.44
MAFFMA0495.3chr6:33825640-33825655AGGCTGACTCAGCAG-6.03
MAFFMA0495.3chr6:33825640-33825655AGGCTGACTCAGCAG+6.09
MAXMA0058.3chr6:33824939-33824949ACCACGTGCT+6.02
MEOX2MA0706.1chr6:33825081-33825091AGTAATTAAC+6.02
TBX21MA0690.1chr6:33823769-33823779AAGGTGTGAA+6.02
TBX2MA0688.1chr6:33823769-33823780AAGGTGTGAAA+6.62
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr63382438733825066
Number: 2             
IDChromosomeStartEnd
GH06I033856chr63382394133824081
GH06I033857chr63382456133824670
Enhancer Sequence
AGAAAGGAGG CCCGAGGGTG GGTCCCTGCC TGCCCCCAGC TGAGTCCTCC CCTCCAGATC 60
TCAGTTCCTG TAAAGGAAGG TTGCTAGTAC TGTCTGAGGA AGGTGTGAAA GGGAAATGGT 120
AGTCCAGCCG GGAAGGAAGG AAGCAGTAAG AGTTCCCCAA ACAACCTCCC CTCCCTCCCT 180
GGCCCCAGAC TGCACCCTGA GCTCAGTTCT TCCTGGTCTC CCCAACTCCC TTCTGTCCAG 240
CGCAGCCCTG AGGTGCCAGG TCCAGTGACA CAAGGCTCTG TGCTGTGAGG ATGCATTCCT 300
CTGGAGTGGG CCAAGGTCCA CTGGCTGGGG AGGATCTGAA TAGGCCTAGG CTTCAGAGCG 360
CTCCCTGGGC TGAGCTTGGA CCTCGGGTCC AGAGAGACCA TCTCCAGAGA GGAAGGTTGG 420
CTTCAGGGCT GCCCAGCTGG TGCAGATGGG GTCTGGGCCT CTCCAAGAGT GACTCCCACC 480
TGCAGCTCTC TGACCAGACC AGAAACCCGC AGGAAGAGCT GGCGTGAGCC CAGGGCCCCA 540
TGCAGGTACA GAGTGGGCTG CCCTCTTCTG TGTAGCTGCC TCCTGCTTCC CATCAAAAGG 600
CTACAAGGAA GGAGGTTGTT GTTTAGGTGG ATAAACTGGA CCCATGGCTG ACAGCGGCCT 660
CTGAGGTTAC AGTGGAACCT CCCCTCAGGT AGTTCTGAGG CTGGGGAGGC AGTGGGAGAA 720
GCTCAGGGGT AGGGGTGGCA CTTGCTTTCA GGACACAGCA CTTTCCTCTG CTCTGGCAAG 780
CCCTCGGGGG CCCTGGAGCA GCCATGGACA AGTGCCGGGG TGGGGAAAGG GGCTGAGAGA 840
TCTCTGGGGC ATCCTCCCTA CCTGCTGCAG CCCTGAGCAT GGGGAGGGCT GGGGACAGGG 900
GTGACAGGCA CATGCCACAC TGCAGTGCCC ACATCCGCCT CTCCACCCCA CTGAGGCCTC 960
TCTCTGCGGT TGCCTGCTGT GGTCTGGTTT GAGTTTATCA CGCTTGTGGC TAGCTCCTGT 1020
GGCAGGGTGA GGTCTCAAGC CCTGTATCCC CTGGGCTCCC CTGATGTTGG GCTGGGTCCT 1080
GGTAGATGCC CCACAGGTAT TTAACACTCA TGTCAGAGCA TGCCACCTAG CCCAGATGCA 1140
TTGCCAAGAC CAGAGAGGGC AAGGGAGGGG CCCAGAGTCC CCCAGGCAGC TGGCCCAAGA 1200
CCCCCTGGGC CCGGCCAGGG CTGGGGTGGG AGAGGAACCA GTCCCTCTGG ATGTGCAGTG 1260
GGAGGCAGCA CCACGTGCTC CCCGTCCCCC CAGTCTGGGC ACCTGCATCC TCCGAGCTGC 1320
CCCATCACTC TCCCCCTTAT GACAAATGGA GGATGAATAA TTCACGGGTG GCTCTGGCTT 1380
TATGAAGTAT TCATCCCTCC CTGGCCTCCA GAGTAATTAA CTATCTGGCC AGCACACTGA 1440
GTATCTGTAA CAGCCCATTA GCAGCGCCTT GCCCTACGTC AAACTGCCTC TCTGGCTGGC 1500
CCAGGGTGGA TGGGGTCTTG GTTCCACAGC CTGGGTTCTC AGCCTAGAGC CAACTATTGG 1560
ATTTTGCAAC GAGCTGGAGG GTTGCAGATT AGATGCCTTT ATGGGCTTCC AGAGGGAACG 1620
GTTGAGGTTA AGGAGGGTTT TCCGCCTCTG GGGCTAGCAG GGACTTTAGA GATCTTTCTC 1680
CATGTGTGGC TGAAGGGGTC CGGAGTGGGG AGGTTGCTGG CTCCAAACTT CATGCTAGTC 1740
AGTGGCAGAT GAGGGAGCCC CAGTCCAGTG CTCTAGGCAC TAATGAGGCT TCCTGCCCGT 1800
TCCCTCGTCT TGCTCCAAGT GCAAGAATGT CTCCAAAGGG GTGCTGAGAG ACCGGAGACT 1860
ACCCCTTTAC CTTGCCCCAG GCCGCCCACC CCAAGGTGCC TGGGAAGGGG GTCTGGCCTA 1920
GTGGTAGGGA GCAGGGATAC AGCAGAAGTG CCTAGTATTT CCCTGACCAG AGGCTGACTC 1980
AGCAGGGCAT CAGGACTGGC TGCCCTCCCC AGCCCCCTCC ACACCTGAAT CCACTCACTC 2040
AGCACTTCCC ACTTCCCTAC 2060