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

TagContent
EnhancerAtlas ID
HS091-06948 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr11:6459740-6461390 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10500671chr116460026hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr11:6460393-6460412TTACCAGCAGAGGGAGCAG+6.18
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1164598016460049
Number: 1             
IDChromosomeStartEnd
GH11I006439chr1164603016460490
Enhancer Sequence
TGCATTCAAA AGTACTCTCT TTTTGACTGT GCATCCCCAG ATACTGCCAC TCTGCATTTA 60
CACACATTTT TTATCTACTG TGCTTATACG ATATCCTCCT GTGGCCCTAC ACATTCTCAG 120
TCCATCTGTG GACAACAATG TGCTGTCCTT TTGCACATTA CACACTCTCA GTTTGTGCAA 180
ATCCAGTCAC TATTACTATA ACACACATGC CTCTAGCTCT GTACCCAGAC ACTCCTGTGG 240
CACATTTATC TGCAACACTA TCAGTGTTGA CAAACATATC CACAACTGTT CATCCTGCAA 300
TCACCCATAC GTTATTTCTT CATTCATTTC TTCATTTATT TATTCATTCA TTCATTCATC 360
CAAGAAACAG TCACTGAATA ACTACTATAT GCCAGGCATT GTGAGAGGCA CTGAGGATAA 420
CAAGACTCTG TCTTTCACTT CAGGAAGTTC ACTGTACAAA AGCAGAAAGG ACTCCTGCAA 480
TCCTAGCCAT GCAACTACCA AGGTGTAGTG TAAAGAGTGC ACTGAGAATA TAGACAGAGT 540
GCCTAAGTCT GCCTAGAGAA GTTGTGGAAG GTTTCACACC AAAGAGGAAG CATTGGGCCC 600
AAGAGCTGAA AAATCAGCAG GAATTTTCCA GGTTGACAAG TGAGGAAAGG GTGTTACCAG 660
CAGAGGGAGC AGCATGCAGA GCCCAAACAT GAGGAAGCAG TGTGCTCCAA CCTCATGTAG 720
ATTCGTATGG CTGGCACACA GTGAATGTGG CAGGGGAGGA GATAAACCTG AGAAGATAAC 780
CAAGGCCCAG ATCATGAGAC CCTGTGTGCA CTTGGTTTGT AGTAATCAGG CACATTTTGG 840
GGTCATTTAC TGAAACAGGA AACACAGGAG GAAAGGTTGG TTTGTAAAGA AGATGCAAAG 900
CTTAGTTTGG GGGATGCTGA ATTTTAGGTG CCTGTAGAAC ATACAATTGG AAAGAGATGT 960
CTGGAGCTCA GAAAGTAGAT CTAGATCCAG TGTCCACAGC ATAGATATTC CTCAGAGCCA 1020
AGGTGATGGT TGAGATCACT GAGGGAAGGT ATATGGAAAG GCTAGGATGG ATCCCCAAGG 1080
AACATTAGGG AACTGGTTGA GATAGAATGA GACATTTGAG AAGAGAGAGA AAAGAGGCAG 1140
GAGGGAAAAC AAAGCCGACA GTCAGGACTT CCCCAACCAC ACAGCACCTT TGGCAAGGTA 1200
GGAAAAGGCA CCCCTTCCTC TGAGCAGACA CAGCCTGGGT CACATGGGAC TTGGTGAGCA 1260
CAGCAGACTG GATTTCATGC TCCACATGCT CTTCTAGCCA GGTGCCATTG TGTTGGGAAC 1320
AACTTGCCTT GCCCTATGAA GAGGACTTGA TACAGGGTCA TGGAAGGCAA GGGAAGCAAT 1380
TGCCAGAGAA AAAAAGGATG GCCAGCAGTG TGAGGTACAG CAGAGCGGTG TAGAACTAAG 1440
ACTAGGACTG AAGAACAGCC ACTGGATGGT GCACCTGCCA GGCCCACACG CATGCACACT 1500
CCCTTAGCCC AAGCTTTTAC AGGAAAGGAG GGCACATGGG AAAGAAATCT GCTACCTATT 1560
GCTATGGGCT CCATGCCAAG GCCATTTGGG GGAAGGGTCC CCAGTGTCGA TTCCAGCCCT 1620
TTCCAGCCTG GCCCTGATTT TGGCCCAGCA 1650