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

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EnhancerAtlas ID
HS048-02654 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:167134930-167135990 
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:167135074-167135092AGAAGGAAGGAAGGAGAT+6.36
EWSR1-FLI1MA0149.1chr1:167135062-167135080GGAAGGAAGAAAAGAAGG+7.71
EWSR1-FLI1MA0149.1chr1:167135066-167135084GGAAGAAAAGAAGGAAGG+8.01
EWSR1-FLI1MA0149.1chr1:167135070-167135088GAAAAGAAGGAAGGAAGG+8.32
RFX1MA0509.2chr1:167135743-167135759GGTCTCCATGGCAACG-6.38
RFX1MA0509.2chr1:167135743-167135759GGTCTCCATGGCAACG+6.4
RFX2MA0600.2chr1:167135743-167135759GGTCTCCATGGCAACG+6.58
RFX2MA0600.2chr1:167135743-167135759GGTCTCCATGGCAACG-6.74
RFX5MA0510.2chr1:167135743-167135759GGTCTCCATGGCAACG+6.15
RFX5MA0510.2chr1:167135743-167135759GGTCTCCATGGCAACG-6.38
ZNF263MA0528.1chr1:167135063-167135084GAAGGAAGAAAAGAAGGAAGG+7.15
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1167135000167135800
Number: 1             
IDChromosomeStartEnd
GH01I167165chr1167134931167136858
Enhancer Sequence
TTCTATGCAA GCTAGAAATG TTTTCTCACT TTTTCCCTGT GCCTACACAT CTCTATACAC 60
CTTCCTAATC CTGAAAACCC AGAACACAGC TTTATGCTGG CTTGGTACTG AATACCCAGT 120
AAGTGTTGAA TAGGAAGGAA GAAAAGAAGG AAGGAAGGAG ATTTTAAAAA GAATGGATAT 180
TATTTAAAAA AGGAAACACT TGGAAAAAAT TATTTCCACC TTGCTCTTTC TTCTCCCCGA 240
AGCCTCCCCC AATCTCCACC TTGCTAGTCT TCCTTTTTGC GATGCAAATG GTTGAGCAGA 300
CAGTAGTGGG GAGAGCTGCA GGAGAGGTCA GCGGTTAAGC TTAATTACAA GTAAATACAA 360
TTTCTCTGGG GTTGCTGTGG AAAGGAGAGC AGATAAGATC AGCGAAAAGT ACTTGGAGGG 420
CCTTGGAAGA CAGCCCCTCT GCAAATATAG GATTGGCTTT TATTGTTGTT GCTGCTAATA 480
AAACAGATGT TCTCAAAGCA TTCCTCCAAC CAGTGAGAGG GCTGGGGAAA TCGCTATGTC 540
TTTACTGGTT GCTGAAACCA AATAAAAATC AAATTAAAGT TTAATTCACC TCATAATTTT 600
CTTCATGGCA GGTCTGCTCA GCAGCCTTGA GGCAGCGCCA ATGTCCTCCT CCACTGTGGC 660
GTACATCACC CTCAGCCCGG GGACCCCAGA GGTCAGCTGC ACATTTCCCT CGTGGGTGTT 720
TGCAGCTGAA GAAAAGGCCC AGGCTAAGAC GAAAGGGTGT TGGGAGCTGC TGGAAGATAC 780
CAGAAAGGCC TTCCCTCCTC TTCCCGTCTC CAGGGTCTCC ATGGCAACGG GGGGAAAGCT 840
GCTAGGTATT CCAGCTATGT GACCCGGGCC ATGTATATTA CCCAGCCTCC TGAGGGGTGC 900
CAGACCATAA ACACTGAGCC GCCTGCAACC ACAGATGTCA TGCTCCCTCC TATGCTCCTC 960
ATACCCAGGA CAGTGTCTGT GATAAGGAGG GCTCGAGTAA CATTTCATGC ACCCATGCAA 1020
TAAAGTTTCC TATTCAGTTA ATATGAGTGA GGGAATGAAC 1060