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

TagContent
EnhancerAtlas ID
HS110-04718 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr8:27190270-27191410 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZBTB18MA0698.1chr8:27191341-27191354CATCCAGATGTGA+6.07
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_08208chr8:27191183-27193111Brain_Inferior_Temporal_Lobe
SE_09156chr8:27181374-27208460CD14
SE_10868chr8:27181046-27285079CD20
SE_18325chr8:27186895-27191430CD4p_CD25-_Il17-_PMAstim_Th
SE_20066chr8:27187970-27193004CD56
SE_22414chr8:27187957-27191473CD8_primiary
SE_27921chr8:27189260-27194488Fetal_Intestine
SE_28623chr8:27189169-27194496Fetal_Intestine_Large
SE_50221chr8:27189287-27193915Sigmoid_Colon
SE_52630chr8:27189370-27193798Small_Intestine
SE_53591chr8:27189274-27193699Spleen
SE_62276chr8:27181124-27271753Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr82719051427191364
Number: 1             
IDChromosomeStartEnd
GH08I027330chr82718809527194337
Enhancer Sequence
AAAATTTTTG TAGAGACGAT GTCTTGCTAT GTTGGCCAGG CTGGTGTTGA ACACCTGGGC 60
TCAAGCAATT CTGCTTCGGC CTCCCAGAGT GTTGGGATCA CAGGCATGAA CCACCACTTC 120
TTCCCCCTAA TTTGAGGAAT TATATCTGTC CTCACAAAGT TTATAGTATG GTAGGGGAGG 180
CAATACATGA AGATAAAGAA CTGTAAGATA TTTATTTAAC TCTAAGTTAC TTAAAGGTAA 240
ATAATGTGCC ATAAAAGAGG CACGAAGTGC TATGAGATTG CAGGGCAGAG ATTCCTTCTG 300
GCTATGGACT CTGGGAATGC TTCCTGGAGG AGACGGCATT TGGCAAAGCT CTGAAAGGAT 360
AGACAGGATA CACTGTGGGA ACTTGAGATG GTGGCTGTAG TCAAAGAAGA GTATAAATAA 420
CAGCAGAGAG ATGGAGAGGT GTGGTTTGAG TGACTCATTT TGGGTGGAAC CAAGAGTGGC 480
AAAAGGCAAT CAGAGTTGGG GGTGGAACGG AAGATAAGGC TTGGACAGGG AGGCCAATGT 540
GTTTGGGAGT TATCCTGGAA GTCCCAGACA GCCATGGGGC TTTATTCTGA AGGCAGTAGG 600
AGCTGTTGAC CATGCTGACT TCGGTGGAGG TGCGAGGGTC AGATTCTGGT GTGTAGAGTG 660
GATGAGAGTG AAGAGAGCTT GAATTCGCAA GGGAGCAGAT AAGAGAGTGT TGTAATATTT 720
CAGGCCTCAC ACATCTGAAT AAATTGCGTA ACTCAGATAC TTTGCGGTCC TGTGGAGCAT 780
GCAGGCATCC CCTGGAGGCT TCTACTTTCT CTGAGCTGAA ATTGGTTCTT TGATGAATTT 840
GAGAGATATA TAACTTATGA GAACATCCAT GAGAAACCCA CCATTCCTCT TCACCTCTGT 900
CTTCCATATT CTTGATTCCC AGCCTGGCCG CTTCCCCCTG GGCCTCCCCT CTGCTAGGAG 960
TGTGTTAAAT GCCAAGCCTG TCTCAACCTC TATCTGGCAG CACCTTGAAG TATCAAGTCA 1020
GGAATATGCA CTTAGATCCA CAGGCCCCTT CTCCATCATG TCTCCGGTGA CCATCCAGAT 1080
GTGATGATTC CCAGGACCCT CCCTCCCTCC CTTAGCCCTC ACTTCTAAGA GTCTGTAAGA 1140