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

TagContent
EnhancerAtlas ID
HS050-70938 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr9:136704870-136706140 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:136705773-136705791CTCTCCTCCCGTCCTTCC-6.36
RREB1MA0073.1chr9:136705044-136705064CCAGTGGGGGTGGGTTGGGT-6.88
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_01082chr9:136704996-136706245Adrenal_Gland
SE_09683chr9:136704548-136706026CD14
SE_33648chr9:136704730-136711536H2171
SE_54463chr9:136704844-136706133Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9136705000136705600
Number: 1             
IDChromosomeStartEnd
GH09I133839chr9136704521136706198
Enhancer Sequence
TACACGAGGA GGCATTTTCA AGGAGAGCTT GTAAGAGATC ACACAGAGGT ATTTAAGTCA 60
CCCCTCAGTA GGGACTTTGT AAACACTGAC CTCGATTAAA CAGTGTGACA CACATTTGCA 120
CAGAGAATGT CTGAGCAGAG TTCCTGGGGC CACATCCCAG CTGTAACTTA AAGCCCAGTG 180
GGGGTGGGTT GGGTGGAGAC TCTGGTCATT TTGCAACAAG GCCTAGCTCC ACCCCCCACT 240
CCCCGCCCCC GAGGCCATCT TCAGGCACCA GCTGATTTTC CTTCCCGCAC TTACCCCTAG 300
CGTCCCCTAC CCACACCTTG CCCTGTGGCG TTGCCTTGCT CGTTAAGAGC AGGGAATGAG 360
AAGCAGAGAA GGCCAACCAC AGCCTATCCA GAAGTTGTCC TGAGAGCAGT CATCCTGGCT 420
CCCCAGGGGC GGCTGCATCC CTCTCCTCCC ACCAGAGCCT TCCTGAGCAT GCATTTCCTC 480
GTGCCCGGCT TCGGGAAGCA GAGTTTCCCA CTGCACCGCC GAGGGGACGA AGCAGATGTC 540
CGCACAGGAA GCAGAGAAGC CCCAAGTGCT GAGTGCAGAG AAATCCCCAG CAGAGCCCGC 600
GTTGGGCAGC AGCCCCTCCT CCCAAACGAC CCATCCAATC CCACTCCCCA AGCTTCCTCA 660
GCACCCACTC CCCACTCCTG CCCCTGAGCC ACTGCTTGCT CAAGGAGCTC CCCCAGCCCC 720
CAACAGGCCT TCCCCATGAG CTCAATTCTG GGCAGGACAA TCACAGTCCC AGTGCTACAG 780
CCAAATAAGT CACCAGCCAG AGGACACAGA CCAGAAAACA GAACACCCTA CAGGGGTGCC 840
CAAACCCAAA CCCCGAAGGA AGAGCAGAGG AAACACAGCT CCTGCTTCCA AAGAGCTCCT 900
TCACTCTCCT CCCGTCCTTC CCCGGGGAAT TACGGGGCAC CTGCGTGGGG CTGGCATGGG 960
CGGCCATTTG TCACTGATTC AGGGAGAAGG AACAGCTTGA ATCTCGCTTT GGGATAATAA 1020
ATCAGGCTCC TATCCTTGCC CTCAGGACTT CTGTGAAAAT CTGCTAGAAA CGATGGCGTC 1080
TGCAGGGCAC CACCTGTGCC ACTCACTGTG CCTACAGCTG CATGGTGGCC CCACAGTCCA 1140
GAGGGAGGGG CACATTGGAC GCGCAGGGGT CTCCAAGCTG AGGGTAGCAA GCACAGGTCT 1200
GTCAGTGCAG ACCCTCAGGA TCTCAGCTAG AGGGACGACA GCTTGGGTTT GCTTTCTTGG 1260
AGGGCCCTGA 1270