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

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EnhancerAtlas ID
HS040-25519 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr3:49334140-49335300 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs3774800chr349334768hg19
rs35395347chr349334797hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr3:49334417-49334428TGGGTGTGGCT-6.14
MSCMA0665.1chr3:49334834-49334844AACAGCTGTT+6.02
MSCMA0665.1chr3:49334834-49334844AACAGCTGTT-6.02
MYF6MA0667.1chr3:49334834-49334844AACAGCTGTT+6.02
MYF6MA0667.1chr3:49334834-49334844AACAGCTGTT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr34933447849334785
Number: 1             
IDChromosomeStartEnd
GH03I049296chr34933428149334430
Enhancer Sequence
TTGTCAATTC AAATTCATCT ATAAAAGAAT TTGTTTTTCC AATGGTTGGC CCATAGGCCC 60
TCTGAAAATT CCTTTGTTGG TGGTCTGCTA AGCTCCCCAC AGGGTAATCC TCCAGTTCCT 120
TTCAGCTCAG GTGTGTGAAA ACACTACTTT CTGGAATTTA CAGAGACCAT GTTAAGGGCT 180
TGGGGTTATA TGTGAAAGTG GACTTTCCCA TGTTCTAGCC CTTGGCACAG TGTCAGCTCT 240
TGGCTGTGTC TGTGCAAGTG AGAACAGAAA TAGATCTTGG GTGTGGCTAG GAACTATTCC 300
TTTTAGAGAG ATCTAGAAGT CATAGGCCCA AAAATGTAAA GGGAAGGAAC TATCTCCTTT 360
ACATACTGAA TTCCTCAGCC AAAAACAAAA ACCAAAACAA AATCCTAAAA CCCTTTCTCA 420
GCAGAGGCAA GTTCCTGAGT GAGAGGTAAA GAGGGAGGGA CAGTACGGCT GTGCTCCATA 480
CTTCCTGGGC AAGTGGCTGC CTGGGAGCAG CAGGCAAGTT CATGTATGGG AGCAGCCGGC 540
AAGTTATTAC ACCACTGTGC CTGGAAGAGG GACACACACA CAATTACACA GAGCAGCCAT 600
GAAGCAGCAT GTGGGAAGGC AGAGGAGGCC TTTGTATTGT CCTCACAGAG ATGAAGAAAC 660
TCAGTCTCAG AGCTTACAGA ATGTTTGAGC TGAAAACAGC TGTTTAAATC AGCCCTGTCA 720
TTTCTGCATT GGGGATGGTA GTATCATGGT ACTCGCTGAG AAGCTACAGC CTGTGGCAGA 780
GAAAGGACAA GATCCTTCCG TACCACACCC CTACTACCAT CTTCCCATCA CACAGCTGGG 840
ATTCCTCTTA AGAAAGGCAT CTCTGATGGT AGGACCATCT GTAGGAGCAG TGATTTGGCC 900
TTCTTCATAG GCAAAACTGT TGAAAAAAGG CTGTGGCTGT GCTGAGGAGA GTTATCAGAA 960
TGTTTAGCTC TGCAGGGCAG GAGGGGTTGA GCACTGATGG CTGCCCACGA TGCCCTCAAT 1020
ACCCATCTCT TGCACCCAGG GGTCAGGGCC AATCCACATG AGCAATGACT GCCCACATTT 1080
TTGTTCTGGA GATATGAATG CAGCAAAGTC TCTAGAATGT GTCCTCTGAC CTGACCTGCA 1140
GCAGAAACTG CTGAGTACTC 1160