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

TagContent
EnhancerAtlas ID
HS108-17196 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr17:46697300-46698510 
Target genes
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Spz1MA0111.1chr17:46697907-46697918GCTGCTACCCT-6.02
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_39949chr17:46697189-46698555K562
SE_47101chr17:46628526-46699689Panc1
SE_56734chr17:46685753-46705899VACO_400
SE_56820chr17:46685753-46705899VACO_400
SE_57368chr17:46696158-46701540VACO_503
SE_58204chr17:46693138-46711614VACO_9m
SE_68498chr17:46671549-46704938TC71
SE_68499chr17:46671549-46704938TC71
SE_68500chr17:46671549-46704938TC71
SE_68501chr17:46671549-46704938TC71
SE_68502chr17:46671549-46704938TC71
SE_68503chr17:46671549-46704938TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr174669740046697600
Number: 2             
IDChromosomeStartEnd
GH17I048618chr174669623246697530
GH17I048620chr174669795646698411
Enhancer Sequence
AGCACCGGCT GGGCCTGGGT AGCCCAGGAT GGGGCAGGAG CCTGGTCTAC ACCAGCTGTA 60
AAGCCAGATT CATTTTGCAT CCCTAATGAA ACCCTCTTTG GAGGGTGCCT GTCCGGGCCT 120
GCCTGATGCG GAGCTCCGCT TTCTCCTGCC TCCCGCCGTC TCTTGGATCA GTTCGTCCTT 180
TCGTTGGAGG AGGGTAGGCC TGGCCTTTTC ACTTGCAGTC TCCCTTCATT CGGGCCATGC 240
TTCGTTCCCA ACTCTACCCC AACTCGCAGG GTCTCCGCGG GCCGCAGTGT TGCCGGCTTG 300
GGTTGGGGAG AGGCTCCTGA GGTAGGCGGG CTCGGGAGCG CCGGCCCGCC GAAGCGGAAT 360
CCCAAGGCCT GGATGAGAAG CGCAGGCTGC CGAGAACTGC GATCTTCATA AGAGGCTCTG 420
GCGAAATCCC TCAGTCTGAG AGGGACAAAA ATGTGCCTCT TGAAACTGAG TTTAATTCTG 480
GGGTCCTTTT GGGAGGTGAA TTTTTCTACT GAGACATTTC TGCTTCACAC TCAATGACCT 540
CTCCACCCTT TGCAGAGGTG CTTACCCAGG GCTCAGCCCC TACCAACCCA GCCCACCTCA 600
GACCAAGGCT GCTACCCTGT GGCTCAAACT GGAGCCTCCA ACCCCAGGTG GGGGCCGAGA 660
ACCCTAAGGC GTTGGCTCCC TTTGAATGGA AGGAAAGAGA TTCCAGCCCT CTGGAGGCCT 720
CTGTCTAGAC CTAGGCACCC TACTGCAGGG AAGAACAGAG GGAAATTACT GTGTTCCTCC 780
CTTGCATCAT ATTTTAAAGC GGCCAAACTA AGGTGACATT CTCAGTGGCT GAGGGAGGAG 840
AGCTACCCCC AGGAGGTGCA GGAAGACCTA CCTTCCCTCC TATTCTCTAG TCAATGAGGA 900
GGTTTCAGGA CCTCATTGCT CCCCAGACCC TGTGCCCTCT CCAAACAACC CACATTTCCT 960
TCCCTCCCCG CTCGTTTTCC AGTTCTCCTG TTGGAAGGCT CTTGATCAGT TTAACCAGTA 1020
GTCTTGGGAC CTGGGGTCTG GGACTGGCTC TCAGCTCCAC CTCTAGAGAG CTCTGCAGGG 1080
GACCTTGCCC TGCAGGGTGT AAGGAGAAAC CTCCTGGACT CAGCAATCTT TTTTTTTCCA 1140
AGCCTTTCTC CCGACAACTG GGATCTCTAC CTATGGTCAG GCCCAGAGAG CCAACACAGA 1200
ATAAGACACA 1210