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

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EnhancerAtlas ID
HS146-09577 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr21:34755150-34756170 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr21:34756066-34756077AGCCACACCCT+6.02
USF1MA0093.2chr21:34755676-34755687GCCACGTGACC+6.62
USF2MA0526.2chr21:34755674-34755690GCGCCACGTGACCCAG-6.69
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_00219chr21:34750982-34756583Adipose_Nuclei
SE_09780chr21:34750609-34758167CD14
SE_10653chr21:34751101-34757835CD19_Primary
SE_10924chr21:34750502-34759616CD20
SE_27036chr21:34754548-34756615Esophagus
SE_36753chr21:34754454-34756616HMEC
SE_53413chr21:34751185-34757173Spleen
SE_58466chr21:34731200-34786233Ly1
SE_60169chr21:34732700-34761220Ly4
SE_60632chr21:34732666-34757447DHL6
SE_61512chr21:34731229-34778660Toledo
SE_64665chr21:34754499-34756570NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr213475529634756154
Number: 1             
IDChromosomeStartEnd
GH21I033378chr213475110834757769
Enhancer Sequence
TGGTGGTGCG TGCCTGTAGT CTCAGCTAGT CAGGAGGCTG AGGTGGGAGG ATCACTTAAG 60
CCTGGAAGGT TGAGGCTGCA GTGAGCGGTG ATGGTGCCAC TGCACTCCAG CCTGGATAAC 120
AGAGCAAGAT GCTGTCTCAA AAACTAGCAA ACGAAACAAA AGGAGAAACT GCTGGCAGCC 180
CCTAATCTAG TACTGTCCCG GCTCCACCCA CCTTCAGATC CAGCCTCCTC CCCTGGCACA 240
CGGGAGCCCC CTCCTCTGAC TGTGCTGAAA GTGAGGGAAG ATCCCCTCTG GGGAGAGAGC 300
TGTAGCCTTG ACCTCTGCAC ACCTTACTTA TCCAGAGCAC GAGGCAGGGC CGCTGACTCA 360
TCCTGGTTTA CCCTGGGCTT TCCCAGTTTC AGCACTGAAA GTCCCGCATC TGGAAAAGCC 420
CCTGAGTCGC TGACAAACCA GACAGTCCGG ACCATGCAAA GCACAGTGCA TGGTGCTTTA 480
GCCACAAAGT TGATTGAAAA GTCAGAGGCA GTGAGCCACA GGAAGCGCCA CGTGACCCAG 540
ACTGCGAGGA GGACACAGGA AACCAACCCT CACTGTGTCC TGCTAGGGGG TTAACCCGTC 600
TACAAGCATC AGGGTTGCCA TTTCAGAGAT CAGCAAACTG AACAGCAGTC GTGACTTGTC 660
CTCGCCTGCA AGACAAGCGA GTAACAAATC CATGAAGGGA AGGACACGGA ATTGAGCAAG 720
GGGGCAGGGC CGGATGTCAT TTTGGCGTTT TTTTTTCTTT CAGTGATTGA GGTAAAATTC 780
ACATAACATA AATTAACCAT TTTAAAGTGT ACGATTCAGA GGCATTTGGT ACATTCACAC 840
TGTTGTGCAA GCACCACCTG TATCTCGTTC CAAAATATTT TCACTTCCCC AAAAGGAAAC 900
TGTGTCCCCA TCAAGCAGCC ACACCCTACT CCCTCACCCC CGCCCCCAGC CTCTGACAAC 960
CACCAATGTA CCTTTTGTCT CTATGGATTT GCCTTTACTG AACAATTCAT AGTAATGGAA 1020