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

TagContent
EnhancerAtlas ID
HS145-15647 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr22:24255560-24256700 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr22:24255933-24255951ATTTCCTTCCCTCCCTCC-6.45
KLF16MA0741.1chr22:24256256-24256267GGGGGCGGGGC-6.02
KLF16MA0741.1chr22:24256352-24256363GGGGGCGGGGC-6.02
KLF5MA0599.1chr22:24256257-24256267GGGGCGGGGC-6.02
KLF5MA0599.1chr22:24256353-24256363GGGGCGGGGC-6.02
SP1MA0079.4chr22:24256351-24256366CGGGGGCGGGGCTTG-6.23
ZNF263MA0528.1chr22:24255838-24255859CTCTTCCCTTCTTCTTCCTTC-6.61
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_37758chr22:24249966-24257197HSMMtube
SE_56738chr22:24255405-24256233VACO_400
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr222425599724256450
Number: 1             
IDChromosomeStartEnd
GH22I023907chr222425015724258315
Enhancer Sequence
CCAGGGGTTA AGAGGGAGCT TGAGGCACCA GAAAGAGCTA TAGTCACAGC CACCTGTGAA 60
AGCCATCTCT GAGGTCCCTT CCTGTCACAA CAGCTGGGCT CCTGACTCAG ACCAAGACAG 120
CTTTTGTTTC TTTTCCTTTC TAGCCCCCCA CTTCCCACCC ACCTTTCTGC TTTCTCATAT 180
GGGCTCATTA TGGTTTATAG GGCTGGGGAA CGTTGCCTCT TCTGCCCTCC ATTTCTCCCA 240
TCTCCCTTCT TTCCCCTCCA CTTTTTCTGA GTCCACTTCT CTTCCCTTCT TCTTCCTTCC 300
CTCTGGGACG CTGCACAGTT CCTTCCACCC GGCACGGCCT GGGACTCTAG ACTCCCTCTG 360
AAGGCACGGA AGTATTTCCT TCCCTCCCTC CGACCCGATC TTTCTGCCCT TGATTCAAAA 420
CAATCTGAGG TCCCTAGGCC CTTCCCTTTC CGCCTCTGCG CTCCCCATGG GGTCCGGTGT 480
AGTTTTCCCG CCCCTTCCCT GCAGCTCCCG AGACCACCCG GACACAACGG AGCCATCCAG 540
CGCCCTCAGA GGCCCTGGGC ACACGGGCAG ATGGTCACCG CCTCCTAAGG GAGCAGCGCG 600
CGCCCGTTGC TCGCTGCCCG TTGGTTGTTG CTGGTAGCTC CGGAGGGCGG GGTTGGCGAG 660
GAAAGTGAGT CCGTATGTCC CCAGCATGCT CCGCGCGGGG GCGGGGCTCT AAGGGGGCAG 720
GCGAAGGCGG AACTGGCGTG GTCAAACCAA CCTATCAGCC TCCAGCATGC TCCGTGTGGG 780
AGCGGGGTTC CCGGGGGCGG GGCTTGGTTT GTGTGCCCTT CCGGCGTTTC GCCCCTGCGT 840
TCTCTGAGAT GCTCCCACGC AGATGTATGG GCCTAATTCG CTAATATCCA CTCTATATCC 900
TGTTCCATCC TCTTGTAATG GGCGTTTGGA GTGTTGCCAA TTTTTTGCTG TTATAATGAT 960
TGTAATAGCA TATTAAAAAA CTTGAACATA GTTTGATTGT AATAACATTA AATATAGCAT 1020
CTTAAACATA CAGTTTGAGC GTGCCAACCT GATGGGTGTG GAATGTAATA TTCATTATAA 1080
CTTTGATTTT CATTTCCCTA CTTTGAGTAA GTTTGAACTT CTCTTTATGT AATTATTGAC 1140