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

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EnhancerAtlas ID
HS177-11808 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr2:42599150-42600210 
Target genes
Number: 10             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs72798544chr242599605hg19
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:42599272-42599290GGAAGAAGGGGAGGAAGA+6.44
HNF4GMA0484.1chr2:42599180-42599195AAGGGGCAAAGGTCA+6.51
Lhx3MA0135.1chr2:42599834-42599847TAATTAATTAGCC+6.32
NR2C2MA0504.1chr2:42599180-42599195AAGGGGCAAAGGTCA+6.67
Nr2f6MA0677.1chr2:42599181-42599195AGGGGCAAAGGTCA+6.73
RxraMA0512.2chr2:42599181-42599195AGGGGCAAAGGTCA+6.53
ZNF263MA0528.1chr2:42599281-42599302GGAGGAAGAGGGAGATGAGAC+6.31
ZNF263MA0528.1chr2:42599273-42599294GAAGAAGGGGAGGAAGAGGGA+6.35
ZNF263MA0528.1chr2:42599278-42599299AGGGGAGGAAGAGGGAGATGA+6.49
ZNF263MA0528.1chr2:42599272-42599293GGAAGAAGGGGAGGAAGAGGG+6.56
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr24259931442599569
Number: 1             
IDChromosomeStartEnd
GH02I042371chr24259836142600103
Enhancer Sequence
AGGCCCTGAA GCCCTGGTCT CACCCCTTGC AAGGGGCAAA GGTCAAGCCA AGGGGTCACA 60
GGTAAGGGGA AGCAAAGTGT TTTTAAGCAG GGCACAGGTG GGCAGCAGCA GACCAAGCTC 120
TGGGAAGAAG GGGAGGAAGA GGGAGATGAG ACTTTTCAGG TTAAGAACAA ACAAGGGAAA 180
GATTCAGTAA GCAGGCAGCT GGGAGCCACA TGTCTGGGCC AAACAACAAG CTTTTAAAAA 240
TCCATAAAGG GCAAGCACTG CATAACAGCG CTCTCTGATG TCAGAGTTCT GCCCTGGCCT 300
TGTGAAAAGC ACCAAGGACT CACCCTGCAG CAGCCAGTCC CTAAATAGTG GGGTGGGGGC 360
TGGTATATCC CAGGCAGCTG GAGGGTGCAC AGAGCAGATG CACCAGACCA GGCTCTGCAG 420
GCCTGGACAG GCAGCTCAGC CAGGCCTGCT TCATTGATAT AGGCTCCTAA TGAGCAGGAT 480
AAACACCATT TGGGGCCATT TGCTGTGAAA TGGGCTGGGG TGTATGAGAA ATTAGCCTTG 540
TATGGGCATA AAACACACAT ATCAGCAGAA AATAATGTGC TGGAAAAGTT TAAATTGAAG 600
ACATGCCATT CTGAGTGTGC AGAGGCGTTA ATGCTTATGT AATTAATCAT TTCATATGTG 660
AAGATTGGGA TTTTTTTTCC CTTTTAATTA ATTAGCCAGT AGACTCATTA TAGTACATTT 720
TTCATGTCAA AAAGGCAGTG GGTTCTAAGA AAAGGGAGGG GGGCTGTAGG GGAGAAGTGA 780
CAGTGTGTTA TAGTGTGATG TGGAAAGTGC AGGGAACCAC CATCCCTGCT CGGAAGAATC 840
CCTGTGGAGG GTGCAGAAAT CCAGAACTCA GCAAAATGCT TTTGACTTAT TCAAGTCCCA 900
TGAATGCAAG ACTGCTGGTG CTCACATTTC CCAGAACCTG CATTTAGCTC CTTTCCAAGA 960
GCTGCTGCCT ACTCAGCTAA TCTGTCTGTC TTTTACTAGA AAGAGGATGC AGCAAGAGGG 1020
CTAAAGGTTA GACTCTGAAG CCAACCAGCC AGATTCCATC 1060