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

TagContent
EnhancerAtlas ID
HS062-00863 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr1:117027140-117028570 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr1:117028046-117028065TGCTGCCACCTGCTGGTCA-8.19
ESX1MA0644.1chr1:117027378-117027388ACCAATTAAC+6.02
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_27848chr1:117025880-117028311Fetal_Intestine
SE_41250chr1:117025585-117028233Left_Ventricle
SE_47846chr1:117027355-117027932Pancreas
SE_50584chr1:117023434-117028613Sigmoid_Colon
SE_52493chr1:117023308-117028704Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1117027705117028232
Number: 1             
IDChromosomeStartEnd
GH01I116481chr1117023899117028464
Enhancer Sequence
TCAGGAGTTC AAAACCAGCC TGGGCAAGAT AGCGAGACCC CATCTCTACA AAATTTTTTT 60
TTTAATTGGC AGGCATGGTG GCATGTGCCT GTGGTACTAG CTACTTGGAG GCTGAGGTTT 120
GAGGATCTCT TGAGCCCAGG AGGTCAAGGC TACAGCAAGC CATGATCGTG ACACTGCACT 180
CTAGCCTGGG TGACAGAGTG AGACCCTGCC TCTAAATAAA TTAAATCAAT CAATCAATAC 240
CAATTAACTA ACTAACCAAC CTGTCTATCG GGGTCAGTCA GCTCTTATAG TCCCACCTGA 300
ATTCTGCTTT GCCTTCTCCT GCAACAGCAA CGCCTTCGAA AGTGCTTACT GTGTGCTAGG 360
CAGGCGTTGC ACATGGACAG GGACTGGGAG TTCAGATGGC CAGCTGGCCT GCTGTCTGGG 420
GACAGGGGGT TTCCCAGGAC CTGAGACTTT CAGTACTAAA ACCAGGACAG TCCTGGGCAA 480
GCTGGAACAG CTGGTCACCT GGTGGGAACT GAGCACCCAT GGAGTCAGCA GAGAAGGAAG 540
GCGGCACCAC AGCATAGCTG GTGGTGGGAG CAAGCAGGAG TCTTTTCCTC CTTAGCACTG 600
GAAGCGCCAC TCTTGGCATT TACCTCCCTT CCTGAATGGA GCCCCACCTG TTTTTATGAG 660
GCCTCCCCAG GCCAAGCCCT CAGGATGGGC AGGGGTGGGT TGAGACTGTG CTGTCTCTGC 720
TGTTTGCTAA GGTTGTTCTC ATGGTATCAC GCTGCCAGAG ACTGTCCACT TGGCTCACAT 780
TGATGGAGGT CAGCTAAGGA CAGGCTGATT AGCTGGCCCC TCAGGGCCTT TCTCTTGGTG 840
ACACAGCCTC TGGCTCAGAA CAAAGGCCCC TCATTTTGCT GAGGCACAGA CTCTTGAACG 900
TGAGAGTGCT GCCACCTGCT GGTCACAGCG CTGCTTCCAG AAGGGGAGCT GGAGCCTCAG 960
GAGGGAGACT GGGCCATGAG CCCAGGTCTG TAGCCTCTCT GTGGGCCACA GCACCACCTC 1020
CCAGCATGCC CTGGGCCAGA TAGCTGAAGA AAAGAAGCTG GGGACCCCCC TAACAGGTAT 1080
GCCTTGAAGG GGACTGCAAG GCTCTCTCAT GCCAGAACTC TCTCAGGCTG GCCATGGATT 1140
CCCAGAATTC CCAGCCAGCG TGGGCACTCT TAGCTATAAT AGAACCCTCG GCCCAGTGGT 1200
GTGCTGGAGC TGCTGGGCAG GAGGCAATCA TCAAATATTC AGGAAATTTA CCAGCTGCAC 1260
TGGTCATGGT GGGAGTATTT ACACCATGGA AATTGGCAAA GGCTACAGAT TAAGAGTTTT 1320
CTCCACCCGT AACTCTTCCT CCAGTGGATT TATCAGTACA CCTTTGCAAA ACCTCTATCA 1380
AACTTAAAAT GTTGTCACCT GAGAAGGGGC AAGTACCAGC CTGTTTGTAA 1430