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

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EnhancerAtlas ID
HS048-02115 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:116253460-116254340 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr1:116254263-116254275GTTTGTTTGTTT+6.32
SOX10MA0442.2chr1:116254275-116254286TGCTTTGTTTT-6.02
ZNF263MA0528.1chr1:116254169-116254190TCCTTTCTCTCCTCCACCCCC-6.07
ZNF263MA0528.1chr1:116254014-116254035TCCCCTTTCATCTCCTCCTCT-6.83
ZNF263MA0528.1chr1:116254163-116254184TCTTCTTCCTTTCTCTCCTCC-7.41
ZNF263MA0528.1chr1:116254166-116254187TCTTCCTTTCTCTCCTCCACC-7.4
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1116253980116254177
Number: 1             
IDChromosomeStartEnd
GH01I115713chr1116253961116254110
Enhancer Sequence
ACCAGGAGGT TTCCCACGGC AAGCGACTGG CCTCTGGGAA TCACATCTTT GTGGGAGGAG 60
AAACTGGTGA TTATCCTCTT CTGTTTCCCT GGCAGGGACT GGTGGGAATG AGCCTTCACC 120
AAGCCCTAGG GGACCGGTCC CAGGCCAGGC ACAGCCAAGT CAGGAGCCAA GGCCACATTC 180
GGCAGAGGCT CATGTGTCTC AGACCAAGCA GTGGTCCAGG AGTGAACAGG TCCACAGCAT 240
GCAGCCTGCC CTGCCCTGCT ATCTGTCCTC ATGGCCCCAC TCCTGGGGGA GCTGGCTGTG 300
CTCACTCCAC AAAGGCACGG AAAGGGACCC TTCCTGACTC CATGCCATGG GAAGTTCTGG 360
GCCTCAGGGT CTCTGCTCCT GTGAGGAGAG GCCTGAGCTT GGGAGGGCCA AGCTCTTAAA 420
GTGGGGTCCT GCCCTTGCTT GTGTGGCAGG TGGACAGATA AACGGCCGGG GCTGGAACCA 480
CACAGCTTAG AGGTTGTGTC TAAAGAGGGC ACTGGGTCTG GAGTTTAAAG ACCTTGCACA 540
GGTTGCTTAA CCGCTCCCCT TTCATCTCCT CCTCTGAAAG TGGAGAGAAC AGCTGCCACA 600
TGACTTCTCA GGCATGTTGA TATAACGAGA TGCTATCAGC ATGTGGGTTG GGCAAAGTGT 660
GTAGGGAGAC ACATGCAGAA GGTCCTCATA AAGACTTTGT CTGTCTTCTT CCTTTCTCTC 720
CTCCACCCCC ATCAAACTCT TACTCATTTT AAGATTTTTT TTTTTTTCAC TACTTTGATC 780
CTTCGTTGAT GGGAAGGGTT TTTGTTTGTT TGTTTTGCTT TGTTTTTGTT TTTGAGATGG 840
AGTCTCACTC TGTCACCGAG GCTGGAGTGC AATGGTGTGG 880