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

TagContent
EnhancerAtlas ID
HS161-15634 
Organism
Homo sapiens 
Tissue/cell
PC3 
Coordinate
chr9:127071230-127072750 
Target genes
Number: 3             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10986311chr9127071493hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EGR3MA0732.1chr9:127072556-127072571GGCGCGTGGGCGGTG-6.07
KLF5MA0599.1chr9:127072253-127072263GGGGCGGGGC-6.02
TEAD1MA0090.2chr9:127072129-127072139CACATTCCAT+6.02
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_02294chr9:127071077-127073507Astrocytes
SE_36996chr9:127070937-127073241HSMMtube
SE_38009chr9:127070839-127073760HUVEC
SE_38868chr9:127070902-127072975IMR90
SE_42506chr9:127071142-127072959Lung
SE_44293chr9:127071327-127073011NHDF-Ad
SE_44809chr9:127070951-127072112NHLF
SE_44809chr9:127072148-127072885NHLF
SE_45648chr9:127066562-127074062Osteoblasts
SE_47283chr9:127070482-127073970Panc1
SE_51779chr9:127071170-127072962Skeletal_Muscle_Myoblast
SE_63558chr9:127071170-127072976HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9127071600127072600
chr9127071472127072577
Number: 1             
IDChromosomeStartEnd
GH09I124308chr9127070962127074018
Enhancer Sequence
TTGGAGGTGG CGACGGAGCA GCCAGGCCTT CCAGGCCAAG GACACAGTTC ACCCTTTCCC 60
TTCTGCTGAG AGCCCCCAGG TGCACCAGGG CCAGGACTCT GCTGGCCCAG GCAGCTGCCC 120
CCAGGAGCCT GGTGTCTCAA GGTGCCCCAC ACCTGAGCAG AGGCCACCCT GGGGACAGCG 180
TCCTGTGGCA GCCCTGGGAG TGCAGTGGTG CCCCAGAGCC TGCTGGACCA TGTCCCCAGC 240
ACACGTGCTC CATCTAGGAA GCTGCCCCAC CAGAGGAGCT GGCCTCTAAT TGGGTCGGAT 300
GGACTGTGAC AAGAAATGCA AATCTGGGTC ATCCATATGC GTGTGAGCAG CTGGAGCCCC 360
AGCCACCTCC ACCCACATCC ACCAGGAGCT TCGGCCCCAC TGTGGAGCTG CACGGTGTAG 420
CCTCCCAGGA CGGGCAGTGT TGGGAACCCC GGCCAGACTC CCACTAGTCA CAGTAAGAAG 480
CCTGGTCTTC CAGGGCAAAG ACCCTCAGGG ACCACTTCCT CCAAACCCTT CACTGTGCCT 540
GGGGGAAACT GAGGCCCAAG AGGGGAGGGA GCCCACCCCC ATCACCAGCA GTGCAGCTGG 600
CTCTAGATCT GACAGGGAGT TCTAGCCTGT TTCCTGATTT GCGAGATGGG ATTCATAACC 660
CTTGCTTCAT GAAGCTATTA GGAGTTTGGA GACATAGAGC TGTCTAAGCA GCTGGAAACT 720
AGCACATAGT AGGCGTCTAA CGTACAACAC CTCATGGTTA TTTTTATGAG TACGTGCGAT 780
TCTTCTAAGT GCTCAGAAAG CCGCCCTGGC TGTTTATGAG GGTATGTGAT TTTGGCTGCA 840
TTCCTAGAGG TGACGGCGTC TGAGTCACAG AGTCCCACTG TGCGCCAGGT CGTGTCAGGC 900
ACATTCCATG TGTCATTCCA CAAACATGCT CCAAGCAGTT GCTCTGGGGT CAGAGCCTCA 960
GTGCAGAGGA CGTGGAGGGG ACTAGACAGG GGCCCCCTTT TGAAGAGGCC GGTGGCGGGT 1020
CCTGGGGCGG GGCCTGGGGC AGGGCTCAGG TGACTGAAAG AATGGAGGCT GGAGCAGGAA 1080
GTGGCAGGCC TGGCCGGTCA GGGGGTCTTG AGTGAAAAGC CGAGGAGGGA TCTGAGCTGA 1140
GAGCCCACCC GATACGGAGC AAGAGCTTGG GCACCACAGT CCCCAGTCCT GGGGTCACAC 1200
CCCAGCTCTG CTGTTCTTTG CTGCCTGATC AGAACAGGTC ACTGCTACCC CTCCAAGCCT 1260
CAGATTCCTG AAATGGGGAC AGCAGTGAGG CCCACTCACA GGGTTGTTCT GAGGACCCAA 1320
AGAGTGGGCG CGTGGGCGGT GTCTGCACAG AGCCCAGCAT GCAGTAGACA CTCAGGATGC 1380
CTGCTCTTCT TAGGTGGGTG CTCTGTGTAC AGGTGTATTT ACCCGACAGA CATTGGCACA 1440
TGGTGGATAA AATCATCATC TTCCTCCTCC AGCAGCCCTC CAGATCGGGT CCTCTGGCAG 1500
GACCCACCAT GAGAGGTAAT 1520