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

TagContent
EnhancerAtlas ID
HS091-24479 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:49111700-49113130 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2617805chr1949112295hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr19:49112512-49112533TCTTTCTTTCTTTTTTTTTTT+6.25
KLF16MA0741.1chr19:49113110-49113121GGGGGCGGGGC-6.02
KLF5MA0599.1chr19:49113111-49113121GGGGCGGGGC-6.02
Nr2f6(var.2)MA0728.1chr19:49112703-49112718TGAACTCCTGACCTC-6.22
SOX10MA0442.2chr19:49112252-49112263AAAACAAAGAC+6.14
SP3MA0746.2chr19:49113109-49113122GGGGGGCGGGGCG-6.11
ZNF143MA0088.2chr19:49112226-49112242CTCCCACAATGCACCC+6.47
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr194911224649112556
chr194911202949112498
chr194911295649113010
Number: 1             
IDChromosomeStartEnd
GH19I048608chr194911188849112613
Enhancer Sequence
TTTTTTTTTT TTATTTTTTG AGACAGAGTC TCGCTCGGTC ACCCAGGCTT TAGTGCAGTG 60
GCGCGATCTT GGCTCACTGC AACCTCCACC TCCCAGGTTC TAGCGATTCT CCTGCCTCAG 120
CCTCCCGAGT AGCTGGGACT AGAGATGCAT TCCACCAGGC CCGGCTGATT TTTTGTATTT 180
TTAGTAGAGA CAGGGTTTCC CCATGTTAAT CAGGCTGGTC TGAAACTCCT GACCTCGGGT 240
GATCCACCTG CCTCGGCCTC CCAAAGTGCT GGGATTACAG GTGTGAGCCA CCACGCCCAG 300
CCCAAAAGCT GTGTTTTAAC AAGCGCTCCC AGGGATTCTG GTGCATGCAC AGGGTTGAAA 360
GCCACTGTTC CTGAGCAGTG TTCTCAGCTG GGCACCTGTG CTCCCCAGTG GGCATCTGCG 420
CTGTCTGGAG AGGTTTTCGG TTCTCTAATT GGCAGGGAAA GTCGGGGGTA TGGGGCGTGT 480
GATGCTACTG ACCTCTGCTG GGTGGAGGCT GAAGATGCCG AGGAGCCTCC CACAATGCAC 540
CCAACAGCTC CTAAAACAAA GACTTACCCA GCCCGAGCGT GGGTGCCACC CCTGTTGAGG 600
GACCTGGTTC TAGAGGCTCT AACCCTATCA GCCCATGACA TAGAGGGGGA AACTGAGGCA 660
CAGAGAGGTG AAGTAAGTTG CCTGAAGTCA CACAACGAGG AACTGAGAGA GCTAGAATTT 720
GAATCCAGGC CGTCTGGTCC CAGAGGCCAC ACCCCTCTCC TCCCTAGCTG TGCTGTGACC 780
CTGTGAGGTA GGTGCTGTTA TTATTTGCAG TTTCTTTCTT TCTTTTTTTT TTTTTTTTTT 840
TTTTGCTTTT TTGAGATGGA GTCTTGCTCT GTCTCCCAGG CTGGAGTGCG ACAGCGCGAT 900
CTCGGCTCAC TGCAACCTCT CTCCTGGGTT CAAGCAATTC TCCTGCCTCA ACCTCCCAAG 960
TAGCTGGGAA GACAGGGTTT CACCATGTTG GCCAGACTGG TCTTGAACTC CTGACCTCAG 1020
CCAATCTGCC CGCCTCAGCC TCTCAAAGTG CTGGGATTAC AGGCGTGAGC CACCATGTCC 1080
GGGCATTTTC TTAGATGCTC AGAGAGGTGG AGTTATTTAC CCGAGGCAGA GCTTAGATCC 1140
CAATCCAGGT GCTCCTGATT TTGAACAAAC CCCACCCCCA AACTGTTTGC CCAGTTTTCC 1200
AGATAAGAAA ACACCAGGTC AAAGAGAAGC AGACTTACCC AAGACCACTA AACAGGCCAG 1260
CACCAGGTCC GGCCGCGGCA CCAACCTCCT CCGCAGGGAA GAGTGTTTTG CCCCCATTAC 1320
ACAGATGAGA AAAGAGAGGC CTGGGCAAGG GGATGCCAGC TGTTCTCTGA GCACACTGAG 1380
GGAAAGTGGG GTATAGGACG CCGGGAGGTG GGGGGCGGGG CGGGGGCTAC 1430