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

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EnhancerAtlas ID
HS047-21989 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr21:34755010-34756220 
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
CAGGCCGAGC TGTGATGGCT CATGCCTGTA TTCCCAGCAC TATGGGAGGC TGAGGCAGGC 60
GGATCGCTTG AGCCCAGGAG TTTGAGACCA CCCTGGGCAA ACCTATCTTT CCAAAAAAAT 120
ACAAAAAGAT TAGCTGGGCA TGGTGGTGCG TGCCTGTAGT CTCAGCTAGT CAGGAGGCTG 180
AGGTGGGAGG ATCACTTAAG CCTGGAAGGT TGAGGCTGCA GTGAGCGGTG ATGGTGCCAC 240
TGCACTCCAG CCTGGATAAC AGAGCAAGAT GCTGTCTCAA AAACTAGCAA ACGAAACAAA 300
AGGAGAAACT GCTGGCAGCC CCTAATCTAG TACTGTCCCG GCTCCACCCA CCTTCAGATC 360
CAGCCTCCTC CCCTGGCACA CGGGAGCCCC CTCCTCTGAC TGTGCTGAAA GTGAGGGAAG 420
ATCCCCTCTG GGGAGAGAGC TGTAGCCTTG ACCTCTGCAC ACCTTACTTA TCCAGAGCAC 480
GAGGCAGGGC CGCTGACTCA TCCTGGTTTA CCCTGGGCTT TCCCAGTTTC AGCACTGAAA 540
GTCCCGCATC TGGAAAAGCC CCTGAGTCGC TGACAAACCA GACAGTCCGG ACCATGCAAA 600
GCACAGTGCA TGGTGCTTTA GCCACAAAGT TGATTGAAAA GTCAGAGGCA GTGAGCCACA 660
GGAAGCGCCA CGTGACCCAG ACTGCGAGGA GGACACAGGA AACCAACCCT CACTGTGTCC 720
TGCTAGGGGG TTAACCCGTC TACAAGCATC AGGGTTGCCA TTTCAGAGAT CAGCAAACTG 780
AACAGCAGTC GTGACTTGTC CTCGCCTGCA AGACAAGCGA GTAACAAATC CATGAAGGGA 840
AGGACACGGA ATTGAGCAAG GGGGCAGGGC CGGATGTCAT TTTGGCGTTT TTTTTTCTTT 900
CAGTGATTGA GGTAAAATTC ACATAACATA AATTAACCAT TTTAAAGTGT ACGATTCAGA 960
GGCATTTGGT ACATTCACAC TGTTGTGCAA GCACCACCTG TATCTCGTTC CAAAATATTT 1020
TCACTTCCCC AAAAGGAAAC TGTGTCCCCA TCAAGCAGCC ACACCCTACT CCCTCACCCC 1080
CGCCCCCAGC CTCTGACAAC CACCAATGTA CCTTTTGTCT CTATGGATTT GCCTTTACTG 1140
AACAATTCAT AGTAATGGAA CCATACAATA TGTAGTCCTT TGCGACTGGC TTTTTTTACT 1200
CAGCATCAAT 1210