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

TagContent
EnhancerAtlas ID
HS104-00367 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr1:10693700-10695450 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs61776290chr110694907hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr1:10694635-10694646GGGTGACTCAG+6.02
JUNBMA0490.1chr1:10694635-10694646GGGTGACTCAG+6.02
KLF5MA0599.1chr1:10694988-10694998GGGGCGGGGC-6.02
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_02060chr1:10690589-10696715Aorta
SE_26713chr1:10690557-10694022Esophagus
SE_26713chr1:10694024-10696856Esophagus
SE_31374chr1:10691440-10696898Gastric
SE_33519chr1:10694710-10698955H2171
SE_41555chr1:10694417-10695415LNCaP
SE_42099chr1:10694033-10696874Lung
SE_54510chr1:10694488-10696720Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr11069410810694152
chr11069464510695194
Number: 2             
IDChromosomeStartEnd
GH01I010630chr11069035210694022
GH01I010634chr11069417710697663
Enhancer Sequence
CTGTGTACAG GGGCTTCCCA CCTAGGGACT GGCCACCGCC TGGCCAGGGG GAGCCACGCC 60
CGAGCTGGCA CATGCTGACA TGCATGTGCG TGCACATGTG TGTGGCACCC TCACACTCAC 120
GCAGGGCCCA GTGGGCCCTT TTCAAGAGGT CCCCATGTCC TCCTCCAACA CGTGCCCATT 180
GCAGGCCACA GCTCAGACCA CAGCCTTGGC ACTCTCTTTA ATGCAAAACG GGTCTGAAAT 240
CTCGCCTGGC ATTGAGGGAT GACTACCTGA ATCATGAATA AACCTTAATA ATTTACTTTC 300
ATTGAGCACT TTATAGTTTG TGTTCTCCTA GAAGAAGAAA TGAGATACAT GATATGTTCA 360
TCAGAAAGAT GCCTGAAACC TTTCCTTGCT CCACGACAGA TACTGGAAGG ACCTTCTTTC 420
AAGCGACAGG GTCATGGCTT TAAACACCAC CATGACACTT GGCATCCAGA TGCGTTATAG 480
CCCCAGGGGG AGGAGCCAGC CTCAGGGAGG CTCCGGGCAG CGAGGTTCTT TCTTGGGGAT 540
CCCTGCCTCC TTCCAGTGGT GTGGGGCATG GGGCTTACTG GAGGCCAAGC CACTGGGTCC 600
AGCTGCTCCA GCGCTGGCTG TGGGCCCCCT GGGAGCTGCC GATTCCTCCC TGACCTGCCC 660
CAGAGGGTGC GGAGGCACCT CCCAGCAAGG ATGGCCGGGG CCTGGCTGCT TCATTCTCAG 720
ACAAGGCTCT GGGATTCCAG CCCTTCAGAG GGCACTGCTG CCAGCCCTGG TCCTAGACCA 780
ACGCTACCTG TGGGGCCAGG GCCACCTCCC GTGACAGTGG ATGGGCAGCT GGCCTTTGCC 840
CAGTGGCCTG GTATGCTGCC CAGAAAGGGG GCTGCCTGTC GCCATGTCCA GGCTGGGGCA 900
AGGCCGCTTC GTGAGCGCCA AGGCCCGGCG CCCACGGGTG ACTCAGGTTG CTGGTGGCGC 960
CCCTGCTGGG CCAGGTCCGT GGGAGGTGGG CAGGCCCCTG AGCTCAGCCC TGAGCCTGTG 1020
CGGCGGGTTC TGGCCCTTTC CAGGAGGTTG CAAAACACTT GAATTTGCCC CAGTTTGGGT 1080
GTAGGAGCAT CACACACCAC AGCTAATTAA ATCCCAGAAG GAAAGCATGC TTTACTGCAT 1140
TTCCTACTGA GTCCAACAAG CCACAGGGAG TGCCGTGGGA CCTGGGCCCA TCCCAACCCG 1200
CAGCTGCAGG CCCCCTCCCG GCTCTTGGGG GCGGTCTCAG AGTGGGCAAC ACATGCCTGG 1260
TGGGGGTACG AGCTTCTCTC CACCCTCTGG GGCGGGGCCT GGGATGTGGC ATCATGGGCT 1320
GGCCTGGGTG CAGCGTCCTG AGGCCTTGAG ATGCCTCTGA GAGGTCCCCG AGTCCCCGTT 1380
CCCCTTCCTT GGGCTGGACT CGGGGCCCTG CTTGTCGTGA GGTTGGTTGA CCCTGGGTGT 1440
GGTCCATCCA GGCCCAGAAG ACCAGGGGGC AGTTTTGGGG TCTGGCCAAG GTCAGCAAAC 1500
CACCCTGAGT CCCCATTCTC CCTCCCCTGG GCCCCAGGAG TCAGTGCTGC CCCAGAGAGC 1560
TGCCCACTGT GCCGGAGCCT AGAGGGAGCT CTGTGGCTGC ACCACCCACC CACCGGCTGC 1620
TCAGGGCTTG GCTCCCTGCC TCGCTTCAGG CCCCACGGGA GGCCCACCAG GGCCTGGGAA 1680
GCTCCAATAA TGGTTTTAAT TTGTTGAACT TGTGTTTTAT CCCATAAATT AGTCACTGTT 1740
TTATTTAACA 1750