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

TagContent
EnhancerAtlas ID
HS139-52888 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr8:27440090-27442190 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs4732728chr827441521hg19
rs7844965chr827442064hg19
rs73229090chr827442127hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr8:27441404-27441418TGTCCCTGGGGAGT-6.05
GSCMA0648.1chr8:27442155-27442165GGGGATTAGC-6.02
Klf1MA0493.1chr8:27440894-27440905TGGGTGTGGCC-6.62
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_28379chr8:27440292-27443297Fetal_Intestine
SE_47912chr8:27440730-27441251Pancreas
SE_47912chr8:27441395-27442601Pancreas
SE_65621chr8:27440297-27442598Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr82744060027441156
Number: 1             
IDChromosomeStartEnd
GH08I027583chr82744058627443184
Enhancer Sequence
GAAGCCCAGT CCAGCCCTGA GGCTCCGAGC CTGGTGGAAA AGAACACATG TTGTAGTTTC 60
CTTTTCACGA GATCAACTCA GGCTGCAAAC ATTCACTAAC CCCTGTTCTT GTCCCCGCCC 120
CTGTCCCCAA CACTCTACCA GTGGGCAGCA GCCATCAGAA GCAGTAAAGG GTTTATTTTT 180
CTCTTTTAAT GTTGTTATTT TTAAAGGGTC TCACTCTGTC ACCCAGGCTG CAGTGTAGTG 240
GTGCAGTCAT AGCTCACTGC AGCCTTGAAC TCCTGGGCTC AAGCGATCCT TCCATCTTGG 300
CCTCCCCCGT GTAGCTGGGA CCACAGGCGC GTGCCACCAT GCCTGGCTAA TTTTTTGTTA 360
TTTATTTATT TATTTTCTTA GTAGAGACAA GGTCTTTGTT GCCCAGGCTG ATCTTGAACT 420
CCTGGCTTCA GGCGATCCTC CCGCTTCAGC CTCCCGGAGT GCTGGGATTC CAGACGTGAG 480
CTACTGAACC CAGCCAGCAG CTAAAGGTTT AAATGTACCA CGTGTTCTTT GTATGCCAGG 540
CCTGCACTGG GTGTGTCATT CCTTTTAATT TTTGCAGCAT CCCTAGAAAG TGACACATTG 600
CCCTTACTTT ACAGATGAGG AAACTGAGGC TCAGAGAGGT ATCTCCAGAG GGTCTGTGAT 660
GAGCAGCCAG GATGGGATCA TAGGACTCAC TGGCTCCAGC TGAGCCCTAG GCTGGGCTGT 720
AGTGTTTTCT CCCAAGCCAG GCAGCCCGAC AGAGTCCACA CCAGCAGCAG AGCCTGGGGG 780
ACCCACTGGA GTTCATGGCA TTTCTGGGTG TGGCCAAGAT TGTTCCGCTT TAGGTCTGAA 840
CCAGGAATCA AGGGACAAGT CGGCCTCTTT CCTCCAGAGG ATCGGCCTCT CCCCAGGGGA 900
GGGGGACTAC AGGTGGCACT AGAGGGACCC CACTAAACAA ACCATGAGGA AGACTAACTG 960
CCTGAAAGGT GCTGGGAAGT GAAACACAAG AAGCCACGTA TTGGATCTGG GCAGGGAAGG 1020
GCCAAAGAGC AGTGAGGGAG ACCAGCCCAA AGGCCTTGCT CTGTCTGGGT TACAGATTTG 1080
GGGTGAGAAT GGAAAGGGCC CCGCAGGCTT TCTCTCTGTG GCCTCAGCTC CAACACAGCT 1140
GACAGCTTTA TGTGCCTGTG TCTGTAGAGC CGGAGCTGAG CCAGGGAGCT TCCCAATAAA 1200
TTAAACTCTA AATCACACCT GCCACCTTCC GGCGAACAGC CAGAAGCTCC AAGAGAGCTC 1260
CAGGGCCTCT GAGCTCAGCC CACGTGGCTC TCCGGCTTAG CAGCTTCAGC AAACTGTCCC 1320
TGGGGAGTGA GCCAGGGCCA GAGACACACT CAGCGCCTGT GGTTAGAATA ACCCTGTGCC 1380
CTGGGGCCTG TGGAAGCTCT GCCATGGCCA GGCTGGTCCC CAAGACACCA CAGAGCATCT 1440
GCCTAGAAAG AGGCAAGTGC CCCTCCCCAG TGTGTACTCT GCATATACCC AGACCTGATG 1500
CCCAGAAACT CTGGCTCCTT GGGACAGTGG AAGATGCCCA GGCTGTGGAT TCAAGTGGAC 1560
TTAGCCTCTG ATCCTCGCCC CTCACTTACC TGCTGTGTGA CTCTAGGTAA ATCGCTCTGC 1620
CTCTCTGAGC TGTGGTTTGC CCATATATAA AGTAAAGCTG GTAGCAACAA TTGGGGTTGG 1680
GAGGATTCAG CGTCTAGTCC GCATGAAGGG TGCTCACCAG ATGTGCCCTC CCTTCTCACT 1740
ATGATAAACA AAGATTCTTC ATTCTCCATA CAAGACCCCC ACCTCTGGTG TCATCTGAAA 1800
CCCCACAGGA GGTGCCCTGG GCATCTGGTT TATGGCCCAC AGTGAGATGG CAAGGATGGG 1860
ACAGTGGGAC AGGCTTGTGG GGTGGGAGGG GGCGAACGAC CTCTCCAGTG AATCCAGAGG 1920
AGGGGCTGGG CACTGGCGAT GCAGGCCCAG TAGAGGCAGC AGCGCATTCA CACGTTAACC 1980
AAGCCACAGA GGCCACCAGC TCCAGTCCCA GCCCTATTAT GCAAGGTCGT CAGTGGCTCC 2040
AGGAGAGGCA GGAGCTGCGA TGGGAGGGGA TTAGCACCAG CTCCACTCAG AAGGCCTGAG 2100