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

TagContent
EnhancerAtlas ID
HS176-39163 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr8:11748480-11749540 
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: 2             
ChromosomeStartEnd
chr81174853511749453
chr81174916711749418
Number: 1             
IDChromosomeStartEnd
GH08I011890chr81174811011750077
Enhancer Sequence
TTGATTGGGG AGGCCCACAA GGCAAGAAAC ACAGGGTGCC TTCTGGGAAA AAACACCTAG 60
GAATCAAGGC CCTTTGTTCA ACTGCCTAAA AGCAATTGAG TCATGTCAAC GACCAAAAAG 120
TGAGCTTGGA AGCAGATTCT CCCCAGTTGG GCCTTTCGAT AAGACTCAAC CTTGCCTGAC 180
ACCTTGAGTG TGGTCTTGTG AGAGACCATA AAATGGAGGA ACCAGCTGAG CTGTGTCCAG 240
ATTCCTGACC TACAGAAACT GTGAGAAAAC GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 300
GTGTGTGTGT GTGAGCCAGA ATCTTGCTTT GTCACCCAGG CTGGAATGCA GTGGCATGAT 360
CATAGCTCAC TGCATCCTTG AACTCCTGGG CTCAAGTGAT CCTCCTGCCT TAGCCTTCTG 420
AGTAGCTAGG ATGGCAGGCA CACATCACCA TGACCAGCTA ATTTAACAAC TTTTATTTTT 480
TGGTAGAGAT GGTATCTCAC TATGTTGCTG AGGCTGGTCT CAAACTGCTG GGCTCAAGTG 540
ATCCTCATAC CTCAGCCTCC CAAAGTATTG GGATTACAAG TGTAAGCCAC TTCACCCTGC 600
CGATGTGTGT TGTTTTAGGT GCCAAATTTA TGCTCCTTTG TCACTCAGCA GTAAATAGCT 660
AAGACAATCC TAAACAAGGT TTTTGAGATG GTAGAATAAA GACTCTCTGG GGTCCAATTA 720
GTATTGGCCT GAGGCAGATT CCCTGAACAG AAAAGGAAGT GACCAGTAAA TCTGAGTCAT 780
CTGGGATGAG GCCCCTTGTT ACTAAACCCT CAGATTCCTT CCTGATGAAA TGAGAAGTTT 840
GGATAGCTCT CCAAGATCCC CTCCCCTCCC CTCTCCTCTC CTCCCCTCCC CTCCTCTCCT 900
CTCCTCTGTA TTTTATTTTC TTTTGAGACA GAGTCTCACA CTGTTGCCTA GACTGGAGTG 960
CAATGGCGAG ATCTCAGTTC ACTGCAACCT CCACCTCCTG GGTTCATGCA ATTCTCCTGC 1020
CTCATCCTCT CGAGTAGCTG TGGTTATAGG CGCACACTAC 1060