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

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EnhancerAtlas ID
HS010-02508 
Organism
Homo sapiens 
Tissue/cell
B_cell_blood 
Coordinate
chr2:109647680-109649030 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFFMA0495.3chr2:109647739-109647754TGGCTGACTCAGCAC-6.13
MAFFMA0495.3chr2:109647739-109647754TGGCTGACTCAGCAC+6.15
MYCNMA0104.4chr2:109648138-109648150GGCCACGTGGGC+6.27
MYCNMA0104.4chr2:109648138-109648150GGCCACGTGGGC-6.27
ZNF263MA0528.1chr2:109648354-109648375GCCACCTTCTTCCCCTCCCCC-6.09
ZNF263MA0528.1chr2:109647806-109647827GAAGGAGCGGAAGGGAGGAAA+6.17
ZNF263MA0528.1chr2:109648361-109648382TCTTCCCCTCCCCCCACATCC-6.1
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2109648298109648660
Number: 1             
IDChromosomeStartEnd
GH02I109030chr2109646813109650140
Enhancer Sequence
CAAGGTGTCA GCAGTGAGGG GGGCCTGTTC CTCACAGATG GGGGCTTCTT GATGGGTGCT 60
GGCTGACTCA GCACAGATGG GGGCTCTGAT GTGGCAGGGG TGGGGTAGAG ACGGGAACGC 120
TCTGCAGAAG GAGCGGAAGG GAGGAAACAG CTTCCTCCAG CCTTCTTATA AGGTTATCAG 180
CCCCGTTCCC CTTACGACGG AATCACTTCC CTGGAGGCCC CCTCTTACTA CTGTTGCACC 240
GGGGACTGGG CTTCAATCAG TAGCAGCAGG GGATGCGCGC TCAGACCCAG CAGTCGGCTC 300
TGCCCGCCTC GCCGGGCTGC ACCGAGTCCG CGGGTCTCTA GCGCACGGCC TGGCCCCACG 360
TGCGGCGAGG AGGGCGCAGT GAAGTTCTGC TGTGTGCACC CCCTGCAGCT CGGCCGGGAA 420
GCGCCCGCTG GAGGAACGGA GAGCGCCGCT TCAGCGTCGG CCACGTGGGC CGGGCTCTGC 480
CGGTGGCAAC CTGGACGCGC TGCGGGCGCC GGCGAGACCT GCGCCAACGC CTACCTCCGG 540
GCCACAGGCG GGATAAAGCT GCCCCACTTT GCCCCCAGCG AAGAGAACCC TCCTTCCTCT 600
AAGTATTTTC TTCAGCAACT AAGCTTTTCT GTTTGCTCAA TTTCTTGTCC CGTGAGCGCT 660
ACCACCCACC CCCCGCCACC TTCTTCCCCT CCCCCCACAT CCGTTCACTC TCTTTGACCT 720
TTTGCCAAAA CTCTGAACGC TCGCTGCCCT CCCTCCCATT TCCTCACCGC GTTTCAGGAG 780
CTGTAAGTTC TTGGTGTTCA AACCCCCTAC GGTTACGTAA ACAGAACTCT GCAGTTATCT 840
TCTTTCCCTT TCTTCGGAGC TTTGTTTTCA AGTTCATTAG AGACTTCCTG TGGGTGTAAT 900
TACCGCTCTG CAGTTTTGAG CGCTGCCCAC CTTCCCCCTG TTTTGTTAAA AATGTCATAG 960
ATCTTTGGAG ATTTCTTTCA CTTCTAAAGT TATTACCTGT CTGCCTGCAC ATCAATCTTG 1020
TTGATTTTAT TTCAGGGCAT TTTCCGGAGT GAACTTCTGC ATAGCGATTT TTTTTGTCCC 1080
TCCCCACCCC CTCTTTGTTT TGCAGGAAGG TGAAATAAGA CAGAAGAAAA GGGTTAGAAC 1140
TTTAGAACTC CAGGACCCAA CCTCAGTCCT TTCAAGCACC GTCTGCAAAC AGATGCTGTG 1200
CTAGACTCAG CACCCTGTCT GGTGAAACTG CTCCTTGGGG TGACATCGGT CGAATGTGTG 1260
AGAGGCTTCA GCGGATGCCC TGACTTTTAC ACCATGGAAG GGCTTTCTCC TCACTCTCCA 1320
TTCTTCATCC CACTCCATCC ATGCGCTTTC 1350