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

TagContent
EnhancerAtlas ID
HS091-17697 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr16:67849240-67851100 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs35316276chr1667850700hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Arid3bMA0601.1chr16:67850866-67850877ATATTAATTAA+6.62
CTCFMA0139.1chr16:67850588-67850607CAACCACCAGGGGGCAGTG+7.69
HEY2MA0649.1chr16:67851010-67851020GGCACGTGTC-6.02
Lhx3MA0135.1chr16:67850867-67850880TATTAATTAATTT-6.37
Npas2MA0626.1chr16:67851010-67851020GGCACGTGTC+6.02
POU6F1MA0628.1chr16:67850868-67850878ATTAATTAAT+6.02
POU6F1MA0628.1chr16:67850868-67850878ATTAATTAAT-6.02
RUNX3MA0684.1chr16:67851038-67851048TTTGCGGTTT-6.02
ZfxMA0146.2chr16:67850113-67850127CCCGCCTCGGCCTC+6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr166785014667850928
Number: 1             
IDChromosomeStartEnd
GH16I067816chr166785028567850939
Enhancer Sequence
AATGCCATCT TTTTTTTTGA GACAGGCTTT TGCCTGTCAG GGTGCAGTGG TGCAGTGGTG 60
CAGTTATGGC TCGCTGCAGT CTCAAATGCC AGGGCTCAAG TGATCCTCCC ACCTCACCCT 120
CCCAAGTAGC TGGAACTATA GGCACATGCC ACCATACCCA GCTAATTTTT TTGGCAGGGG 180
GGGACAGAGT TTTGCTCTGA CACTCTGGCT GGAGTGCAGT GGCACAAACA CAGCTCACTG 240
CAGACTCCAC CTCCCATGCT GAACCAATCC TCCCACTCAG CCTCCTGAGT AGCTGAGACT 300
ACAGGAGTGC GCCACCACAC CTGGCTATTT TTTGCATTTT TTGTAGAGGC AGAGTCTAAC 360
TACGTTGCCC AAGCTGGTCT TGAACTCCTG GGCTCAAGCT ATCCTCCTTC CTTGGCCTCC 420
CAAAGCACTA GGATTACAGG TGTGAGCCAC CACACTGAGC TCAATACTGT TTTTTTTTTT 480
GAGATGGGGT CTTGCTCTGT CACCCAGGAA GGAGCACAGT GGCGCGATCT CGGCTCACTG 540
CAACCTCCGC CTCCTGGGTT CAAGTGATTA TCCTACCTCA GCCTCCTGAG TAGCTGGGAT 600
TACAGGTGCA CACCACCATG CCCGGCTAAT TTTTTTTTTT TTTTTTTTTT TGAGACGGAA 660
TCTCGCTGTC GCCCAGGCTG GAGTGCAGTG ACGCAATCTC GGCTCACTGC AAGCTCCACC 720
TCCCAGGTTC ACCCCATTCT CCTGCCTCAG CCGCCCCAGT AGCTGGGACA GACGCCCGCC 780
AACACACCTG GCTAATTTTT TTTGTATTTT TAGTAGAGAT GGGGTTTTAC CGTGTTGGCC 840
AGGATGGTCT CGATCTCCTG CCCTCGTGAT CCGCCCGCCT CGGCCTCCCA AAGTGCTGGG 900
ATTACAGGCG TGAGCCACTG TACCTGGCCC CAATGCTGTC TTATTAAGTA CTTTTGGGCT 960
CTTGTTGATA TGATCATAGG ATTGTTATTA ATCAGCAAAT AGCCATTGTC CAAATCTCAT 1020
AAAGGAAAAA ACACATTTGA GTAAACTTAC AACTCTGGCT CACAGTGGAA CAGCATGGGC 1080
TGTATGGTGG TTTTCCTTCT GTGACCCTGA CCCTCGTGGG GAATTTGGAA ACACATGGGC 1140
CACACACTTT GTGGGGCTGG GGACTCCCAA CACCCCTGCG GGAGTGACTC CAGGGAGGAG 1200
AAAGGAGGGG TCAGTATGGA TTATTCGCAG AGACCAAGCG CAGCCCAAAA ACCTGATGAC 1260
TAGGGGAGAG CTCTGAGGCT CCCGGGCACC CTTCTCAGCT GCCACCTTCT GTGGGCCAGG 1320
CTTTTTCATT CTTTCTTTTG CGCGGCATCA ACCACCAGGG GGCAGTGTTC CCTCCCGCCG 1380
TCCCTCCGGG GCCGCCTTCC CGTTTTTACC TACAGGGGGA AGCAGAGAGC ACGGAGCGCC 1440
CGGGAGCACT GCGTTCCAGC CACCCGGGCG GAGATCCCTC AGCTGTTAAT AACCTAGCCG 1500
AGACCCGGCC CTGGCAGCTG GTTCTCCAGC TTCCACTCGC CTCTGCAAGC AAAGGAGGGT 1560
AGCCACATTT TCTCCCGGTA GAAACAGTAG ACAGAACACG AGGACTGGTC TTTTTTTTTT 1620
TTTTTAATAT TAATTAATTT ATTTTTTGAG ACGGAGCCTC GCTCCTCGCC CAGGCTGGAG 1680
CGCAGTGGCA CAGTCTTGGC TCACTGCAAC CTCCACCTCC CAGGTTCAAG CGATTCTCCT 1740
GCCTCAGCCT CCCTAGTAGC TGGGACTACA GGCACGTGTC ACCACACCTG GCTAATTTTT 1800
TGCGGTTTTT TTTTTGTTTT TTGTTTTTTT GAAACAGAGT CTTGCTTTGT CGCCCAGGCT 1860