EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-37328 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr9:88676820-88679100 
TF binding sites/motifs
Number: 33             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:88677598-88677616GGAGGGAGGGGAGGCAGG+6.4
EWSR1-FLI1MA0149.1chr9:88677590-88677608GGAAGGATGGAGGGAGGG+6.66
IRF1MA0050.2chr9:88678379-88678400GGGATGAAAGAGAAACTAAAA-6.65
IRF1MA0050.2chr9:88678385-88678406AAAGAGAAACTAAAACTGAAC-7.26
IRF2MA0051.1chr9:88678383-88678401TGAAAGAGAAACTAAAAC+6.13
ZNF263MA0528.1chr9:88677300-88677321GGAGGAGAGAGGATGGGGAGG+6.03
ZNF263MA0528.1chr9:88677346-88677367AAAGGATGGTGAGGAGAGGGA+6.04
ZNF263MA0528.1chr9:88677355-88677376TGAGGAGAGGGAGAGAAAGGA+6.04
ZNF263MA0528.1chr9:88677386-88677407AAGGGAGGACGGGGGAGGAGG+6.12
ZNF263MA0528.1chr9:88677370-88677391AAAGGAGGACAGAGGGAAGGG+6.13
ZNF263MA0528.1chr9:88677430-88677451GAGGGAGAGGAGGAGGGAAGA+6.21
ZNF263MA0528.1chr9:88677587-88677608AGAGGAAGGATGGAGGGAGGG+6.26
ZNF263MA0528.1chr9:88677412-88677433AGAGGAGGAGGGAGAATGGAG+6.27
ZNF263MA0528.1chr9:88677304-88677325GAGAGAGGATGGGGAGGAGGG+6.35
ZNF263MA0528.1chr9:88677322-88677343GGGGAAGGGGAGGAAGGAGAG+6.38
ZNF263MA0528.1chr9:88677373-88677394GGAGGACAGAGGGAAGGGAGG+6.43
ZNF263MA0528.1chr9:88677321-88677342AGGGGAAGGGGAGGAAGGAGA+6.44
ZNF263MA0528.1chr9:88677529-88677550GGAGGATGGAGGGAGGAAAAG+6.56
ZNF263MA0528.1chr9:88677526-88677547AGAGGAGGATGGAGGGAGGAA+6.57
ZNF263MA0528.1chr9:88677389-88677410GGAGGACGGGGGAGGAGGGAG+6.72
ZNF263MA0528.1chr9:88677415-88677436GGAGGAGGGAGAATGGAGGGA+6.72
ZNF263MA0528.1chr9:88677435-88677456AGAGGAGGAGGGAAGAAAAGA+6.82
ZNF263MA0528.1chr9:88677396-88677417GGGGGAGGAGGGAGGAAGAGG+7.07
ZNF263MA0528.1chr9:88677591-88677612GAAGGATGGAGGGAGGGGAGG+7.08
ZNF263MA0528.1chr9:88677313-88677334TGGGGAGGAGGGGAAGGGGAG+7.27
ZNF263MA0528.1chr9:88677599-88677620GAGGGAGGGGAGGCAGGAGGA+7.34
ZNF263MA0528.1chr9:88677426-88677447AATGGAGGGAGAGGAGGAGGG+7.35
ZNF263MA0528.1chr9:88677307-88677328AGAGGATGGGGAGGAGGGGAA+7.51
ZNF263MA0528.1chr9:88677399-88677420GGAGGAGGGAGGAAGAGGAGG+7.75
ZNF263MA0528.1chr9:88677316-88677337GGAGGAGGGGAAGGGGAGGAA+7.88
ZNF263MA0528.1chr9:88677438-88677459GGAGGAGGGAAGAAAAGAGGA+8.04
ZNF263MA0528.1chr9:88677406-88677427GGAGGAAGAGGAGGAGGGAGA+9.07
ZNF263MA0528.1chr9:88677403-88677424GAGGGAGGAAGAGGAGGAGGG+9.18
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr98867695888677011
chr98867706188677256
chr98867783488678737
Number: 1             
IDChromosomeStartEnd
GH09I086062chr98867742088679098
Enhancer Sequence
GCAGGGGACC CAGATGGGCA GAAAGGCGGG TCTGGACCTG CAGCTATGGG ACAGTGTGCA 60
CAAGTCACCA AGTTTAAATG GAAGGGCGTC GGGAGATTAA GTGTAACTTT CTACAAAGCT 120
TCAGAAAACA CCATCTATCC AGGAAAACAC GTAGGACACA CAGACACAGT TGCTACACGC 180
CCAGAATAGC TCCTGCCAAC ACATCCCTGT GTTGTCACAG GGAAGGTAAC ATCCTCCCAC 240
CCCATCCACC TTGCAGCTTG GCGGGTGTGG GAAAGCACCT CGCTGGGAGA GTGCAGGATG 300
CTCCCAGGAC CCGCCCTGGG GTCACCCGGG TGCCCAGCTT GGCAGAACAA GGTCCATGAG 360
GTGTGGTGGC CATCACAGAC ATAAGCACAG GGTTGATGGC GAGGGGGCCT GAACCCAAGA 420
CTGGCTCACA CCCTCCCCCA GCATCTCCTG CACAGGGCAC ACTGCAGGTG CTTTGGGGAG 480
GGAGGAGAGA GGATGGGGAG GAGGGGAAGG GGAGGAAGGA GAGAGCAAAG GATGGTGAGG 540
AGAGGGAGAG AAAGGAGGAC AGAGGGAAGG GAGGACGGGG GAGGAGGGAG GAAGAGGAGG 600
AGGGAGAATG GAGGGAGAGG AGGAGGGAAG AAAAGAGGAC AGAGTAGGAT GGAGGAAAGG 660
GATGGAAGGA AGAGGAGAGA GACAGGGTCT GGAGGGGAGG AGGGCAAGAG GAGGATGGAG 720
GGAGGAAAAG GACAAAGGAA GGGAGAGGGG TGGAGGGACA GAAAGGAAGA GGAAGGATGG 780
AGGGAGGGGA GGCAGGAGGA AGGAAAAAGG AGGAGAAGCA AACGGGGGGG GCTGCCCTTG 840
CCTCTGAGAA CCTGCTACAC TGTCTCCTTT GGTAGCAGCC TGCCCCTGTG CCTCTAACCT 900
ACACGTGACT TGGGTCAAAT AAAACTTCCA GGAGGATCCA AACCTGAAGG ACAGTGGGAA 960
CCCCAGAATG CACTTTGAGG CTTCTCTAGC AGTGGACGAG CGCCTGTCTT CTTAGTCCCT 1020
GACCCTGGAT CTTTCTGAAG GTCTCCTCAT CACCCAGCTG CCAGGGAACC TGGCTGCCCC 1080
TGAAGCAGCT CACACTGGTC TGTCCCCTCT GCAGCACCAC CCAAGCTGCC CCTCAGCTCT 1140
TCCCGCTGCT CTCACTCCTG AACACTTAAG GAGATGGCAG GGGAGGAGCT GCCGAACCAG 1200
AGGAGCACCC CACACACTGC CAACAGGGCT TGACCCAGGA GCGGGGGCTT GAAAAGCTCC 1260
AGCTCCGTTT TTAGAGGAAG AAGAATGCCG GATTACAACA CAGCACCAGC AATCTGGATA 1320
TTCGTTCCCT GGCTGTTCTT TAACCAGCCA GGAAATGCCC TGTGCAAGGG CTGGAGGCCT 1380
GGGGCTGCAG ACTCCCAATC TCAATGGGCA CCCCAGGGCT GAGCCACCTG AGGGCACTGG 1440
GGGTTTCCAT TTTCAAACGG GAATCCTAGC AGCTTCCCTG CTCCCACCTG CGGAAGAGGA 1500
GACACTTTTG TACATTCTGA CTTTCTGCAG ACAGGTAAAA AGGCGTACAC AGACCTTTGG 1560
GGATGAAAGA GAAACTAAAA CTGAACCAAG TGTACAGGTT ACAGCGTCAC AGTCAAGGCA 1620
CCTAACAGAC CCTACTTACT GTTTGTTCTT AAACATGAAT GACTGCAGAT CCCTGCCAGA 1680
GACGGTAAGT GAAAAAACAG CTACCTCCTA TTTTCTTTAC GTATTTCCCA TCAAACGCCT 1740
GTCTTGGGTT GGGTTAAGAA TTACAGAAGG TAAACGGAGT CAATTCCAAG TCACTCAAGC 1800
AATTTTCTGT GTGAAGAGAG AACAAGACAA AAGCCAACCA CAACAGCAAA ACCCAAAGCC 1860
TCCGTTACGC CTTCTATGGC AATCAAACAC GCCAACGCTC TTTCTAGTGC GTATGAAGCC 1920
AAGGCCAAGA GCGAGGACAC CTGCAGGATT TGGTTCTGTC CCATTAGGAA CAGAGATCAA 1980
TGCACATGAA ATCCATGCCT CGTCTGGTCA GCCGCTAACC ATCGTGGGCA ACCTCACATT 2040
GCACGACAAT GCTTTCCATG TGGAACTTGT CCATGGCATG TTTAAAAATC AAACCACGTC 2100
CTGAATCAAA TAGGCATCTG AGTCTTCTCC TGAGGTCCAG GACATCCCAT GACAGGCTCA 2160
GGCCCCTCCC TGGAGGTGGG AGGTGAGGAC CCAGCACTAG GACACCCACT GAGGCACAGT 2220
CTGCAGTGAA GGACATCTAC CTGAATGGCA TGTTTGCTGC TTCTCCTACA AATGTATTTT 2280