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

TagContent
EnhancerAtlas ID
HS091-33448 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr22:50431050-50432940 
Target genes
Number: 1             
NameEnsembl ID
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr22:50431967-50431986CACTGCCGCCTGGTGGCAG-6.19
KLF14MA0740.1chr22:50431421-50431435AGCCACGCCCCCTC+6.73
KLF16MA0741.1chr22:50431422-50431433GCCACGCCCCC+6.62
SP1MA0079.4chr22:50431419-50431434CCAGCCACGCCCCCT+6.31
SP3MA0746.2chr22:50431421-50431434AGCCACGCCCCCT+6.46
SP4MA0685.1chr22:50431419-50431436CCAGCCACGCCCCCTCG+6.55
SP8MA0747.1chr22:50431422-50431434GCCACGCCCCCT+6.92
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr225043145050431800
Number: 1             
IDChromosomeStartEnd
GH22I049993chr225043153150432447
Enhancer Sequence
AGTTTATTAT TTTTAAGATG GTGTCTCATT CAGTCACCCA GGATGGAGTG CAGTGGCATG 60
ATCTCAGCTC ACTGCAACCT CTGCCTTCTG GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC 120
TGAGTAGCTG GGATTACAGG TGCCCACCAC AATGCCTGGT TAATTTTTGT ATTTTTAGTA 180
GAGCTGGGGT TTCCCCATGT TGGCCAGGTG GTCTCAAACT CCTGACCTTA AGTAATCCAC 240
CCGCCTTGGT CTCCCAAAGT GCTGGGATTA CAGGCGGGAG CCACCGTGCC CAGACCCACC 300
CTATTTCAGA TTGCAGCTCC CCACACTCCC CATCGTGCTC CCAGCCTCAT TCCTCACCCC 360
ACACTGGCAC CAGCCACGCC CCCTCGCTTA CTTATGTCAC TTGGCTCTGG TTGTCTCTCT 420
CATGCAAAGG TCAGCTCCAT GATCCCAGTT TGCCTGGGAC TGTCCTGGTG TCAGCACTGA 480
CACTCTGACC CAAGACCCTC CTTAGTGCCA GGCAGCCCCA GACTTGGTCC CCCAGCTGCA 540
GGGCCCGGGA TCTTTGCCAG TGTTGTTTGT TCCCGGTGCT GGGTCGGGGC CCAGGGCCCA 600
AGGCCTGCTC AGCTGTGTGT CATGAGTGAA TGAGGCAGGC GGGCGTCCAA GGCTCACCCG 660
TGTTATACTG TGGCCCAGAT GTGAGCAGGG CTGTGCACCC CAGTACAGGT GCTCCTGCCC 720
GCCCCTACCG CACCCCCCTT TCTGGGGCCC GGGGTCCTCA GCACTTTTCT CCTGGCAGGT 780
GTGGGGGTGG GTTTCCGGCG GTGGTGGTGG AGGGAGGGCA GCGTCCCTGG CCAAGGAGGC 840
GGTGGGTGCA CTGGGCTGTG GGCGCTCCGT GTTGGGTGCT GGGGCGGCTG ATCCGGCTCA 900
GCACCAGCAC TAAGAGCCAC TGCCGCCTGG TGGCAGCACG CGTGTGTCCT CCAGCAGGTT 960
CCTCCCTTGT CTGGGAGGGA CAGTAGGACA GCTGAGATCT GAACACAGCC TCTTAACAGT 1020
CCCCAAAGAC TCAGTTTCCC CCATCTGCAG AAGAAAAGAC TCAGTTTCCC CCATCTGTGG 1080
AAGGCTTGAG GGAGCCCACA CCCGTCAGGC AGGAGCTCAG CTCTGTGACC CTGGTCTGGC 1140
CAATCCTCCC CAGCCCCACC TCCACGGTGG CCAGGATTCC CGGAGTAGCC CTGGGTCAGA 1200
GCAGGGGTCT TTGTGCACCA CAGGGAGCAC CCCTGGCTGG TCCAGGAGGC AGGAGCAGGA 1260
ACCTGGGGCG GGGACTGCCC TGCTGAGCCG GGACACTTGT TTTCTGGCTG GGGGCGGACG 1320
GGGTCTCCAG AGGAGACATG GAGAGAGCAG AGTGGCAGCT TGTGCTGTGC CCCCCACCCC 1380
CACTGTGCCC CTGACCTCCC CCAGGCTAGG GAGGGGCACC TGGGTGAGTG GCAGCCTGTA 1440
TCCCCCCATT CCCCTGATCT CCAGGTTAGG GAAGGGCACC TGGGCGAGTG GCAGCCTGCA 1500
TCCCCCCATG CCCCTGATCT CCAGGTTAGG GAGGGACACC CTGTCCATGC CCCCCACTGG 1560
CCTCCCTGCC CCTGGTGCTC AAACCCAGCT TCTAAAGCCC CTCACCTGGC CTGACCTCCG 1620
CATCCCCAGG GTGTCTCCAC CACTGGTCCT TTATGGGGAC ACTTGGATGG GGATGTCTGG 1680
TCACACCATG TGACGCTGAC CTCAAATCCA CTCCCAGAGA CCCGGCACCT CCCCTGAGTC 1740
CCAAGGTGCT CCCTGCCCCC CACATGCCCA TGGGGGTGCG GCCTCCCACG CCTTTGGGGT 1800
GCTCTTGGGT CCAGCCTGGT GGGGATGGCT CCACGACACC CGCACTCCAG ACTTGTCCCT 1860
GGTGCCGTCA CCATCCAGCC AGGCCCAAGC 1890