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

TagContent
EnhancerAtlas ID
HS139-33632 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr20:56653700-56654770 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs201459901chr2056653725hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr20:56654358-56654370TGCCCCCAGACA-6.44
MAFFMA0495.3chr20:56654156-56654171ATGCTTACTCAGCAA+6.89
MAFFMA0495.3chr20:56654156-56654171ATGCTTACTCAGCAA-7
MAFKMA0496.2chr20:56654154-56654173AGATGCTTACTCAGCAACC-6.18
RREB1MA0073.1chr20:56653731-56653751CCCCCACCCAACCATCACCA+6.64
SOX10MA0442.2chr20:56654202-56654213AAAACAAAGAC+6.14
Stat6MA0520.1chr20:56654130-56654145AGTTCACAGGAAATC-6.01
ZNF740MA0753.2chr20:56653722-56653735CTACCCCCCCCCC+6.13
ZNF740MA0753.2chr20:56653725-56653738CCCCCCCCCCCAC+6.92
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr205665381456654357
Number: 2             
IDChromosomeStartEnd
GH20I058078chr205665385756654057
GH20I058079chr205665406156654230
Enhancer Sequence
CCACCCCCCA CTCCTCCCTG CACTACCCCC CCCCCCACCC AACCATCACC ACCACCACCA 60
AGAGCAAACT CTAAGAGGAT CTCAGGTGTT TTCCTGGATC ACAGAAGCCC AGGGAGCAGA 120
CCCCACAGCT AACACTGACT CATGCCTCTT CCATGCCACC CCCTGCCCCT GTGCCCCAGA 180
GCCTCCCTTG GTTCATTTTT GGCAATCCTT GGTTCCTACA ATTCCTGCAG CTGCCTTGAT 240
TCAAACTCCC TCCCCAACTC CACCCCAGGC TTAAGGGTGG ACTGGATGGG AGCTGCAGGT 300
CATGGCGGAG GTCGGGGGGG ATCTCCAGCC AGTTACACCC CAAGGAGATG GAAATCAAAG 360
CCAATAGAAA CTCCTGTTGT TCACCAGCCC CTTCAAACAT CCTGCTTGGA GCAGATTCAG 420
GCTCTGGAAA AGTTCACAGG AAATCCTGGA GATCAGATGC TTACTCAGCA ACCACAAGCT 480
TTATCTTGGG TCTGAGTCCC AGAAAACAAA GACAAAAGTT TCTTCTAAGA CTCCCTTCTC 540
CCTTCGCCAA CTGGTGGAGC ACCATTTCCA AATAAAGGGG CTCCAAAAGC AATTCTAAAG 600
CAGAACTTGA AAGTCAAATC ACATTCTCAA AGCTCGTGCA GTTAAAACAC GGGTCAGATG 660
CCCCCAGACA GAGTCCCCCC ACAACCCGCC CTCCCACTAG CTGCAGAAAA GCAGCTAGGC 720
TTGAGCCGTT CAATTCAGTA GCCATTAGGA TTATGTGGTT CTTCAGCACC CAGTGTAGCC 780
AAGGAATTGA ATTTTTTAAG TTTAATAAAC TTAAACTTTA AAACTGAACA GTAACATATT 840
TGTCCATGAA GACAACTTTA TTGTTTTGTA GAACTACTTA CTGTATTCAT TTCCAATTGC 900
TACTGTGATG AATTACCAGA AACCTTGTCA CTTAAAACAA CAGGCTCGGT ACAGTGGCTC 960
AGGCCTGTAA TCCCAGCACT TCGGGAGGCT GTGGTGGGCG GATCACTTGA GTCCAGGAGT 1020
TCAAGACCCA ACTGAGCAAC ATGGTGAAAC CCCATCTCTA TTAAAATTAA 1070