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

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EnhancerAtlas ID
HS051-05246 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr11:113235780-113236940 
Target genes
Number: 1             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10789942chr11113236199hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:113236097-113236115CCTTCTTCCCCTCCCTCC-6.04
ZNF263MA0528.1chr11:113236103-113236124TCCCCTCCCTCCCACTCCACC-6.51
ZNF263MA0528.1chr11:113236106-113236127CCTCCCTCCCACTCCACCTCC-7.15
ZNF263MA0528.1chr11:113236093-113236114TCCTCCTTCTTCCCCTCCCTC-7.89
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11113235820113235875
Enhancer Sequence
AGGTATGCTG TGGACACGGA GCCAGGCTGA CCTATTGCAG AAAGAGCAGC TGAGCTGAGG 60
TGCTGAGTTT TGGCTGGGAC TGCATGCCAC ACAGAACAGT GTGGGAAGCC CTCATGCTTT 120
CTGTGCAGAC CTAGGTTAAG CCCAGTAGCT GCTTCTCTGA AGAAAGCCTT TCTAGAGGAA 180
ACTGGGGAGC TCTCGGTCTC CAACCAGAGA GGGAATCGGC TTGTCTGACA GGGACGTGCT 240
GCTCCCACTT GCTGCCGTTG CCTTCTCTCC ATTCCATTCT CCACTGTTTT GCATCCCTCT 300
CCCTGTCTCT TTATCCTCCT TCTTCCCCTC CCTCCCACTC CACCTCCCCT TCTCTTCCCT 360
CTTTTCTCTC TTCTCCACTT TTCCAGAAAC AGACCCCCCA CTTCATGTTC TTTGCCTCAG 420
CCTAAACAAA TGGAGGAACG GCCAGCAAGG GTCACATGTT CATGCAGGAG AAAACAGTGG 480
AGAAGGAGAG ACGCAGAACA GCATGCCGAG GTCCCCAGTG AGCGAGGGCA AGAGATGTGG 540
GCTGTAACTG TGCCCATGGC TTCTCTGTTA GCTCAGACCT CCACTCTGCT CTGCTCCTCT 600
TCTGATGTGC AGACGCATCT CATTGCACGT GCTTTTGGGA GGTGTCCACC TGTGGCTGAG 660
CAAAGGAGCC CTGGCATAGA GCAAGGGTAA CCCCGGGAGC TGAGTGAGAG AGGCTCCTTC 720
CCTTACATCC ACATGCCTTT AATTCCTCCT CTGTAGATTG AGGGGGTTGG CCTTGATAAT 780
ATCTAAGGTC CTTTCAAGTT CTGTCTGGTT GTTCAAATGG AAGGAATAGT TAAAATCTTT 840
CTTCTATAGA AAGAAAGCAC ATTAGCTAGG ATGACTTCAA AGTGGCAACC TATGGGGGAG 900
TTCTCGAGAG CAAGGTCCTG TCTGATCAGC CTGACACACC TGCCACCTGC AGCGAGTGTT 960
TTCAGTGCTT TGTGGGCCTC CCTGAGGGTC TTACTTACCC CTGTGATCTT TAGGGTACCC 1020
CAATGCCACA GCCACTTCCT GTTTCCACCC AGAGTGATAG GACTGACGTT CTCAGCCAGC 1080
TTCCATCTGA GAGGGTGTTG GCTCTGGGCT CCAGAAGCCT GAACCGTGGC ACTTATGCCC 1140
TGGGTTGTTT GTTTTGATTG 1160