EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-18555 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr16:89764980-89767330 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs35432452chr1689765046hg19
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ATF3MA0605.2chr16:89766748-89766760AGTGACGTCATC+6.11
ATF3MA0605.2chr16:89766748-89766760AGTGACGTCATC-6.14
JDP2(var.2)MA0656.1chr16:89766748-89766760AGTGACGTCATC-6.07
KLF16MA0741.1chr16:89766594-89766605GCCCCGCCCCC+6.02
KLF5MA0599.1chr16:89766594-89766604GCCCCGCCCC+6.02
MYCMA0147.3chr16:89766736-89766748GCCCACGTGCCC+6.44
RFX1MA0509.2chr16:89766704-89766720CGCTGCCATGGCAACC+6
RFX1MA0509.2chr16:89766704-89766720CGCTGCCATGGCAACC-6
RFX2MA0600.2chr16:89766704-89766720CGCTGCCATGGCAACC+6.26
RFX2MA0600.2chr16:89766704-89766720CGCTGCCATGGCAACC-6.32
RFX5MA0510.2chr16:89766704-89766720CGCTGCCATGGCAACC-6.69
RFX5MA0510.2chr16:89766704-89766720CGCTGCCATGGCAACC+6.91
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr168976611689766800
Enhancer Sequence
CGTCCCAGGT TCAAGCAAGT TCCCCTGCCT CAGCCTCCCG GGTAGCTGGG ACTACAGGCG 60
CCCACCACCA CACCCGGCTA ATTTTCATAT TTTTAGTAGA GACAGGGTTT CACCATGTTG 120
GCCATGCTGG TCTCAAACTC CTGACCTCAA GTGATCCGCC TGCCTTGAGC TCCCAAAGTG 180
CTGGGATTAC AAGCGTGAGC CACTGTGCCC GGCCTAGAAT TTTTTTTTTT TTTTCTTTTT 240
TGAGACAGAG TCTCGCTCTG TCTGGAGTAC AGTGGCACGA TCTCGGCTCA CTACAACCTC 300
CTCCTCCCGG GTTCAAGCGA TCTTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGT 360
GCGCACCACC ACGCCCCACT AATTTTTGTA TATTTAGTAG AGACGGGGTT TCACCATGTT 420
GACCAGGAAG GTCTTGATCC CTTGACCTCA TGATCCACCC ACCTTGGCCT CCCGAAGTGC 480
TGGGATTACA GGTGTGAGCC ACCGCACCTG GCCGAATTTC TTAAATTTAA TGGAAAAAAC 540
AATGAATACA TTAACCTAGC TCACAAATCA GAACAAAATG AAGAGCCCCT GTACTGAGAA 600
ATTCCACTGT CTTCTGTCCC ACCGCTCCCT TCACCCCTGG AGATGGCCTC ATCTAATTAG 660
TTTTGAATGT ACTTGCCCAG GTGTTTGTTT TGCAAACCCA AATACAGATT TCGTTTGCTC 720
CTCGTATGAG GTAGTCCCCC CTTTTTTTTC ACCTCTTTGT AAGGTCTCTA ACCAAAGCTA 780
GACAGGTAGC CTCTTAAACG TGTTGTTCTG AACTTTGTTT TTTTCCACTA CAGTCTTGCA 840
GACAAGGACA GAAGCTGTAA CGTTCATTCC CCCTGCTGTG TAGTATTCCA CCATGGGGGT 900
GACACGTCTG TTTTCAGCGC TCTCCAGAGG CTGTCCATGC ACTGGGCTGA CAGCCGTGGG 960
ACGGTAGAAG GGTGAGTGCT CTTTTTTTTT TTTTTTTGAG ACGGAGTCTC ACTCTGTCAC 1020
CAGGATGGAG TGCAGTGGCT CGATCTCTGC TCACTACAAC CTCCACCTCC CAGGTTCAAG 1080
TGATTCTCCT CCCTCAGCCT CCTGAGTAGC TGGGATTACA GGCGCGTGCC ACCACACCCA 1140
GCTCATTTTT GTATTTTTTA ATAGAGACGG GGTTTCACCA TGTTGGTTAG GCTGGTGTCA 1200
ATCTCCTGAC CTCGTGATCT GCCCACCTCG GCCTCCCAAA GAGCTGGGAT TACAGGCGTG 1260
AGCCACCGCG CCCGGCCTGG CTGAGTGCTT TCTAGCCTAC ACTTAGGTGA AGAACTAAAG 1320
GAGCTCAGGA CAATCACTGC GAGCGTCTCC TGACTCTCAA ATTCCCTAAC TCCGGGACTC 1380
CTAGCATCTA ATGCCTGGAC ACGGCCCACG TGTGGAGCGC CCAGTGCCTG CAGCACTGAG 1440
CTCGGGGCTT TGATTCATTC CTCTGGCCCC ATGAACTGGA CTGTTCCCGT GTCGCTGTCT 1500
CAGGAGGAAA GGGGCTGACA GAGATTAGCT AATTTGGCCA AGTCCTCGCG GCCAGGAAGC 1560
AGCAGAACTA AGTCCAAACC AGGGCTGTCC GGCACTGAAG CCGGTTATTC CCCCGCCCCG 1620
CCCCCTGGGA GGCCTCAAGG GCGGGCCTGT CCGTCCTCTC TCATGAATGA AAGTCCTGGC 1680
GCCTCCGACC AGCAGGTGTC CCCGGGGAGC CGCGGAGAGA CTGCCGCTGC CATGGCAACC 1740
GGCGGAGGCG TAGCTCGCCC ACGTGCCCAG TGACGTCATC GGCTTCCTAC TCTTCCGAAT 1800
TAGCTCAGAG CTCCCGGCGG CCCTGCCCCC TCCTGCCGCC AGGAGCTCAC CTGGAGAGGC 1860
CAGGCCAGCC CTGGGCACAG CCTCCCGCCC CAGGCCGTGG AGTTCACTAG GTCTGAGCCC 1920
AGCCCTGAGA CTTCACAGGG ATGCACCCAT CTGCAGTCCT CCCAGCCTCG GCGGCCTCCT 1980
CTGCAAATGG GATTGGCCCA TAACCTGGAG GAATTAGGAT GACCATGGGA ACTCAAGTCC 2040
CTTCTGTGCC CCCGTCCTAA GATTTCCATG GCAACTGGGG CCGCGAGGCC TCTTAGGGAA 2100
GACACTGACG CAAGCTCTCA GGGCAGGACC CCGTAGGCAG CACCCAAGCC TGCCCTCGCC 2160
CACCCCATGT TCTCAGCCCT AGGAGTGGGT GCCCCCACAC GCCCACGACC CCTCAGCGCT 2220
CGGAGCCTTG AGGAGCCCAC CAGGCACTGA GGACACTTGA AGCCCCTCTC TCTCGAAAGG 2280
CGTGGTCCCC CATGGTCGGC GGCCCCGCGA CCCGCAGGCC AGGACGAGGG GCGCGCTCCT 2340
CCTGGCCTGG 2350