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

TagContent
EnhancerAtlas ID
HS101-18225 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr17:29826270-29827940 
Target genes
Number: 8             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2097719chr1729827429hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr17:29826515-29826525GGCACGTGCC+6.02
HES2MA0616.2chr17:29826515-29826525GGCACGTGCC-6.02
Nr2f6(var.2)MA0728.1chr17:29827824-29827839GAGGTCAAGAGATCG+6
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_05270chr17:29826467-29828451Brain_Cingulate_Gyrus
SE_06379chr17:29824218-29828558Brain_Hippocampus_Middle
SE_07497chr17:29826240-29828384Brain_Hippocampus_Middle_150
SE_08278chr17:29826362-29828216Brain_Inferior_Temporal_Lobe
SE_31907chr17:29826677-29827730Gastric
SE_35520chr17:29824590-29828086HepG2
SE_47707chr17:29826760-29827564Pancreas
SE_62782chr17:29813392-29838946Tonsil
SE_65467chr17:29826488-29828527Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr172982672929827607
Number: 1             
IDChromosomeStartEnd
GH17I031498chr172982600929828070
Enhancer Sequence
GTGACTCCAA AGGGGAGTAA AGAGAAAAAC TGCAGGATAC TTCAGGGGAA AGTGGATGAG 60
ACTCTCTGGA CACCATTCCC CCACTTTTTC TTTTCCTTCT TCCTTTCTTT CTTCTTTTTT 120
TTTAGATAGA GTTTCACTCT GTCGCCAGGC TGGAGTACAG TGGCACAGTC TCAGCTCACT 180
GCAACCTCCT ACTCCCTGGT TCAAGCGATT CTCCTGCCTC CGCCTCCCGA GTAGCTGGGA 240
TTACAGGCAC GTGCCACCGT GTCCAGCTAA TTTTTGTATT TTTTAGTAGA GATGGGGTTT 300
CACCATGTTG ACCAGGATGG TCTCAATCTC CTGACCTCGT GATCCGCCCG TCTCGGCCTC 360
CCAAAGTGCT GGGATTACAG GCATGAGCCA CCGCACCTGG CCACATTTCC CCATCTATAA 420
GGAGGAAAAT GATAATTACT TGCAGGGAGT TTACCACCTC TGTAAAGCAC AGAGCAGACT 480
GGCCACATGG TAGGCGCCCT AGTATGTCAA CTTTGTTCTC TTTCTCTGAG TTGTGGCTCC 540
ACTAGCTATT TGTAGACAGG AGATCTTTGT GGCTTCAGGT AGGTGATGGG GGACTGAAAG 600
CTAAGAGGAA AAGCCTCCCC TGACCTGCAG CTTCTCTTTG AGCTGGCATG CCTGGAATTC 660
TTGGGGCTGG CTGCTGGGTT TGTTTTCCAG ATGTGGAAGC AATTTAAGTT CTGTTTTCTT 720
AATCCCCAAC AGTTTGCCTC CGAAGTCCAC ATTCTCATTT GAAAATCAAG GCCGTTGGCT 780
CTGTTTGCAG GGCAGAGGGT AGGCTAGATA GCCTCTTCAA ACCCTTTTTG TTTAGGAAAT 840
GGGCTTACTG GGGCACTCAG ATCTGGGACC CAGGGCATTC TTGGGACAGT CACACCCCAT 900
CCAGGACTTG GTTAAAAGGT GAGTTCACTT TCTCTGTGGG TTTTCCTTGG AGATGATTCA 960
CTGAGCTAAA TTCAGCTGCA CCTTGGTTAC AAACCAGCTC TAGACCGCTG TGGAGTGGCG 1020
GGGGTGGGGC TCGGGTTTGG GCCATGTCAC AGGCCAGCTG GCGTCCCTCT GAGCAGGGTG 1080
CCCACGTGTC CCGGGGGCAG TAGCGGCCCT CCTTCCCACA CTGACCACAA CAGAGGGAGG 1140
AAAATGCTCC AGATGTCAGG TAGCCAGAAA TACTGTCTGG CACGGAGAAA CTGGTAATAT 1200
CTTGTTCAGT TACTGAGCGC TGCTGGTCAC AGAGGCAGCC TGACCCAGGA TAAAAGGCTC 1260
CTTGTGTGAG GGCCTGTGGC TCCAGGGCTA ACTGCTGATT TATTCTCTTG TAAAGCAATC 1320
GCTGTGTAGG TAAAATACCT TTTACATTTG TCTTATAACT ATACTAAATA CAGTTTTGGG 1380
CAAACAAAAA TTGCCTTTGC AATTCTAACG TCTCTGAACT GTGCATATGC TTCTCTGAAA 1440
TTGAAATAGA ATACTTATAC TACTGAGAGA ATGCACAAGA AAATGGAAGT GGCTGGGCAT 1500
GGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCTGA GGCGGGCAGA TCACGAGGTC 1560
AAGAGATCGA GACCATCCTG GCCAACATGG TGAAACCCCG TCTCTACTAA AAATACAAAA 1620
ATTAGCTGGG TGTGATGGCA CGCGCCTGTA GTCCCAGCTA CTCAGGAGGC 1670