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

TagContent
EnhancerAtlas ID
HS129-34934 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr8:11748490-11749890 
Target genes
Number: 8             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs55894533chr811749242hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
STAT3MA0144.2chr8:11748519-11748530CTTCTGGGAAA+6.62
ZNF263MA0528.1chr8:11749366-11749387TCCCCTCCTCTCCTCTCCTCT-6.21
ZNF263MA0528.1chr8:11749351-11749372TCTCCTCTCCTCCCCTCCCCT-6.23
ZNF263MA0528.1chr8:11749361-11749382TCCCCTCCCCTCCTCTCCTCT-6.58
ZNF263MA0528.1chr8:11749346-11749367TCCCCTCTCCTCTCCTCCCCT-6.69
ZNF263MA0528.1chr8:11749356-11749377TCTCCTCCCCTCCCCTCCTCT-7.38
ZNF263MA0528.1chr8:11749338-11749359CCCTCCCCTCCCCTCTCCTCT-7.39
ZNF263MA0528.1chr8:11749343-11749364CCCTCCCCTCTCCTCTCCTCC-7.64
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_09230chr8:11747973-11749627CD14
SE_28772chr8:11748723-11749467Fetal_Intestine_Large
SE_46238chr8:11745330-11750396Osteoblasts
SE_56280chr8:11747969-11750403u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr81174853511749453
chr81174916711749418
chr81174947811749546
chr81174958511749659
chr81174968611749795
Number: 1             
IDChromosomeStartEnd
GH08I011890chr81174811011750077
Enhancer Sequence
AGGCCCACAA GGCAAGAAAC ACAGGGTGCC TTCTGGGAAA AAACACCTAG GAATCAAGGC 60
CCTTTGTTCA ACTGCCTAAA AGCAATTGAG TCATGTCAAC GACCAAAAAG TGAGCTTGGA 120
AGCAGATTCT CCCCAGTTGG GCCTTTCGAT AAGACTCAAC CTTGCCTGAC ACCTTGAGTG 180
TGGTCTTGTG AGAGACCATA AAATGGAGGA ACCAGCTGAG CTGTGTCCAG ATTCCTGACC 240
TACAGAAACT GTGAGAAAAC GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 300
GTGAGCCAGA ATCTTGCTTT GTCACCCAGG CTGGAATGCA GTGGCATGAT CATAGCTCAC 360
TGCATCCTTG AACTCCTGGG CTCAAGTGAT CCTCCTGCCT TAGCCTTCTG AGTAGCTAGG 420
ATGGCAGGCA CACATCACCA TGACCAGCTA ATTTAACAAC TTTTATTTTT TGGTAGAGAT 480
GGTATCTCAC TATGTTGCTG AGGCTGGTCT CAAACTGCTG GGCTCAAGTG ATCCTCATAC 540
CTCAGCCTCC CAAAGTATTG GGATTACAAG TGTAAGCCAC TTCACCCTGC CGATGTGTGT 600
TGTTTTAGGT GCCAAATTTA TGCTCCTTTG TCACTCAGCA GTAAATAGCT AAGACAATCC 660
TAAACAAGGT TTTTGAGATG GTAGAATAAA GACTCTCTGG GGTCCAATTA GTATTGGCCT 720
GAGGCAGATT CCCTGAACAG AAAAGGAAGT GACCAGTAAA TCTGAGTCAT CTGGGATGAG 780
GCCCCTTGTT ACTAAACCCT CAGATTCCTT CCTGATGAAA TGAGAAGTTT GGATAGCTCT 840
CCAAGATCCC CTCCCCTCCC CTCTCCTCTC CTCCCCTCCC CTCCTCTCCT CTCCTCTGTA 900
TTTTATTTTC TTTTGAGACA GAGTCTCACA CTGTTGCCTA GACTGGAGTG CAATGGCGAG 960
ATCTCAGTTC ACTGCAACCT CCACCTCCTG GGTTCATGCA ATTCTCCTGC CTCATCCTCT 1020
CGAGTAGCTG TGGTTATAGG CGCACACTAC CACACTCGGC TAATTTTTTT TTTTTTTGTA 1080
GTTTTAGTAG AAATGGGGTT TCACTATGTT GGCCATACTG GTCTCAAATT CCTGACCTCG 1140
TGATCAGCCC TCCTCGGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC ACCGCGCCCA 1200
GCCTTTGTTT GCTTTTCTCT CTTTTTTCTT TTTTGAGACG AACTCTTGCT CTGTCGCCCA 1260
GGCTGTGGAG TGCAGTGGAG CAACCTTGGC TCACTGCAAC CTTTGCCTCC CAGGTTCAGG 1320
TGATTCTCCT CCCTCAGCCT CCCAAGTAGC TGGGACCACA GGAGGGGACA CGCCACCGCA 1380
CCAGGCTAAT TTTTGTATTT 1400