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

TagContent
EnhancerAtlas ID
HS091-06242 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr10:102822860-102824010 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr10:102822918-102822930CGACCCCTGACA-6.32
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_24658chr10:102820165-102823067Colon_Crypt_2
SE_31743chr10:102819840-102827879Gastric
SE_34806chr10:102819113-102828226HeLa
SE_35714chr10:102819633-102824102HepG2
SE_54395chr10:102819793-102827894Spleen
SE_57911chr10:102819931-102822997VACO_503
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10102823000102823816
Enhancer Sequence
GTACGCATGG CCCGGGGCCC CCACCCCAGC ACTTAGGTTT CCTAGAGGCA CTGCTCCCCG 60
ACCCCTGACA GCATTGGTCT CTGGCCAGCA GAGCAAAAAA GATAAGGCTA TAGAGGCCTC 120
GAGTCCAGTA TAAAACCCTG CTCTCGCTAC TGGTTCATAA AAGCTGCCAC CTTAAGGTGG 180
GGGTGGGGGG TGGAGTGGAG TGGGAGTCCC GGGCTTCGTC AGCAAGCTGC ATTCGCTGAA 240
CCACGTGAAA GCTCCAGAGC TGGCTGGCAG GGAGAGACAG GTCCTCTGAG GGCGCAGGCA 300
CATAACCTAT GGTTTGCTCA GAGACCCCCC CGACTTTTCC CAGACCAGTG GAGTCCAGGC 360
AGCAAGACGG GTTCCTGTGA GATGCAATCA CGTTTCATTC TTAGAGCAGT TTGTTCACCC 420
AGTCTCCCCA CCTCTCTGCT TTCTCCTGCT TTTAGGGATT AGTGAAGGGG AGCGGGAAGT 480
TCTTTCTCTA TCCCTGGGGA CTGGGGTCCA TTCAGGCCTC TAGCTTTCCT TGGTAGCTTT 540
AGTAACTTTC ACTTCCTGAG CCCGGGCTCT GCGTCTGGCT CGGCTGGGGC AGCCAGAAAA 600
CAAACACCCC GTGGGGGTCC CAGCAATTTC CTCCACTCCT GCAGGCTTCC TGCCTGTCGC 660
ACAAGTCCAG CTTCAGGTTC TCTGCCTTGC CGCAGGACTC CCCCAGGGGG TACTGAGGAG 720
GGAACGGCTG CTTTTCCTCC TTTGGGAACT GGGCCTGTTT AGAAAAGGGG AAGGGGGATC 780
TGGAAGGTTT TGATTACAGG CACGCAGGAA AGGCTGGGGA GGGTGAAATG AGGACAGGGG 840
AGCAGTTAGG GACAGAGTGG CTGCCAAGCT ACAATGTAGA TGTGTGTGCT TGTTTGTGCA 900
TTGGGTCTGC ATGAGGTTCT ATGTGCACAT GTGCATGTAT ACCTATCTCC ACGTCTGCGT 960
GGTACCCTTG TGTGTACCAG CATCCATATC TGTGTGTACC TGTGTGTGTC ACGGTGTGTT 1020
TATGGATGTG TATTTACCTC AGCATATATT GTGTTCTGCC ACAAGCATGT CCACAAAAAT 1080
TTGTGTATCA TGTCTTTGCC AGACTGGATG CCTTTGCTGG GCCATGCTAT TCTCAGACCT 1140
CCCGCCTTCA 1150